{
  "url": "https://openlegislation.uk/eu-directive-2008-58/annex-1F",
  "json_url": "https://openlegislation.uk/eu-directive-2008-58/annex-1F.json",
  "legislation": "eudr/2008/58",
  "legislation_title": "Commission Directive 2008/58/EC of 21 August 2008 amending, for the purpose of its adaptation to technical progress, for the 30th time, Council Directive 67/548/EEC on the approximation of the laws, regulations and administrative provisions relating to the classification, packaging and labelling of dangerous substances (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-directive-2008-58",
  "path": "annex/1F",
  "kind": "annex",
  "number": "1F",
  "heading": null,
  "text": "Index No\nChemical name\nNotes related to substances\nEC No\nCAS No\nClassification\nLabelling\nConcentration Limits\nNotes related to preparations\n‘006-011-00-7\ncarbaryl (ISO);\n1-naphthyl methylcarbamate\n200-555-0\n63-25-2\nCarc. Cat. 3; R40\nXn; R20/22\nN; R50\nXn; N\nR: 20/22-40-50\nS: (2-)36/37-46-61\nC ≥ 25 %: Xn, N; R20/22-40-50\n1 % ≤ C < 25 %: Xn, N; R40-50\n0,25 % ≤ C < 1 %: N; R50\n006-045-00-2\nmethomyl (ISO);\n1-(methylthio)ethylideneamino N-methylcarbamate\n240-815-0\n16752-77-5\nT+; R28\nN; R50-53\nT+; N\nR: 28-50/53\nS: (1/2-)28-36/37-45-60-61\nC ≥ 7 %: T+, N; R28-50/53\n1 % ≤ C < 7 %: T, N; R25-50/53\n0,25 % ≤ C < 1 %: Xn, N; R22-50/53\n0,1 % ≤ C < 0,25 %: Xn, N; R22-51/53\n0,025 % ≤ C < 0,1 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n006-087-00-1\nfurathiocarb (ISO);\n2,3-dihydro-2,2-dimethyl-7-benzofuryl 2,4-dimethyl-6-oxa-5-oxo-3-thia-2,4-diazadecanoate\n265-974-3\n65907-30-4\nT+; R26\nT; R25\nXn; R48/22\nXi; R36/38\nR43\nN; R50-53\nT+; N\nR: 25-26-36/38-43-48/22-50/53\nS: (1/2-)28-36/37-38-45-60-61\nC ≥ 25 %: T+, N; R25-26-36/38-43-48/22-50/53\n20 % ≤ C < 25 %: T+, N; R22-26-36/38-43-48/22-50/53\n10 % ≤ C < 20 %: T+, N; R22-26-43-48/22-50/53\n7 % ≤ C < 10 %: T+, N; R22-26-43-50/53\n3 % ≤ C < 7 %: T, N; R22-23-43-50/53\n1 % ≤ C < 3 %: T, N; R23-43-50/53\n0,25 % ≤ C < 1 %: Xn, N; R20-50/53\n0,1 % ≤ C < 0,25 %: Xn, N; R20-51/53\n0,025 % ≤ C < 0,1 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n007-007-00-8\nethyl nitrate\n210-903-3\n625-58-1\nE; R3\nE\nR: 3\nS: (2-)23-24/25\n009-001-00-0\nfluorine\n231-954-8\n7782-41-4\nO; R8\nT+; R26\nC; R35\nO; T+; C\nR: 8-26-35\nS: (1/2-)9-26-28-36/37/39-45\n013-002-00-1\naluminium powder (stabilised)\nT\n231-072-3\n7429-90-5\nF; R11-15\nF\nR: 11-15\nS: (2-)7/8-43\n015-003-00-2\ncalcium phosphide;\ntricalcium diphosphide\n215-142-0\n1305-99-3\nF; R15/29\nT+; R28\nN; R50\nF; T+; N\nR: 15/29-28-50\nS: (1/2-)22-28-36/37-43-45-61\nC ≥ 7 %: T+, N; R28-50\n1 % ≤ C < 7 %: T, N; R25-50\n0,25 % ≤ C < 1 %: Xn, N; R22-50\n0,1 % ≤ C < 0,25 %: Xn; R22\n015-004-00-8\naluminium phosphide\n244-088-0\n20859-73-8\nF; R15/29\nT+; R28\nR32\nN; R50\nF; T+; N\nR: 15/29-28-32-50\nS: (1/2-)3/9/14-28-30-36/37-43-45-61\nC ≥ 7 %: T+, N; R28-50\n1 % ≤ C < 7 %: T, N; R25-50\n0,25 % ≤ C < 1 %: Xn, N; R22-50\n0,1 % ≤ C < 0,25 %: Xn; R22\n015-005-00-3\nmagnesium phosphide;\ntrimagnesium diphosphide\n235-023-7\n12057-74-8\nF; R15/29\nT+; R28\nN; R50\nF; T+; N\nR: 15/29-28-50\nS: (1/2-)22-28-43-45-61\nC ≥ 7 %: T+, N; R28-50\n1 % ≤ C < 7 %: T, N; R25-50\n0,25 % ≤ C < 1 %: Xn, N; R22-50\n0,1 % ≤ C < 0,25 %: Xn; R22\n015-006-00-9\ntrizinc diphosphide;\nzinc phosphide\nT\n215-244-5\n1314-84-7\nF; R15/29\nT+; R28\nR32\nN; R50-53\nF; T+; N\nR: 15/29-28-32-50/53\nS: (1/2-)28-30-36/37-43-45-60-61\nC ≥ 7 %: T+, N; R28-50/53\n1 % ≤ C < 7 %: T, N; R25-50/53\n0,25 % ≤ C < 1 %: Xn, N; R22-50/53\n0,1 % ≤ C < 0,25 %: Xn, N; R22-R51/53\n0,025 % ≤ C < 0,1 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n015-019-00-X\ndichlorvos (ISO);\n2,2-dichlorovinyl dimethyl phosphate\n200-547-7\n62-73-7\nT+; R26\nT; R24/25\nR43\nN; R50\nT+; N\nR: 24/25-26-43-50\nS: (1/2-)28-36/37-45-61\nC ≥ 25 %: T+, N; R24/25-26-43-50\n7 % ≤ C < 25 %: T+, N; R21/22-26-43-50\n3 % ≤ C < 7 %: T, N; R21/22-23-43-50\n1 % ≤ C < 3 %: T, N; R23-43-50\n0,1 % ≤ C < 1 %: Xn, N; R20-50\n0,025 % ≤ C < 0,1 %: N; R50\n015-048-00-8\nfenthion (ISO);\nO,O-dimethyl-O-(4-methylthion-m-tolyl) phosphorothioate\n200-231-9\n55-38-9\nMuta. Cat. 3; R68\nT; R23-48/25\nXn; R21/22\nN; R50-53\nT; N\nR: 21/22-23-48/25-68-50/53\nS: (1/2-)36/37-45-60-61\nC ≥ 25 %: T, N; R21/22-23-48/25-68-50/53\n10 % ≤ C < 25 %: T, N; R20-48/25-68-50/53\n3 % ≤ C < 10 %: Xn, N; R20-48/22-68-50/53\n1 % ≤ C < 3 %: Xn, N; R48/22-68-50/53\n0,25 % ≤ C < 1 %: N; R50/53\n0,025 % ≤ C < 0,25 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n015-056-00-1\nazinphos-ethyl (ISO);\nO,O-diethyl 4-oxobenzotriazin-3-ylmethyl phosphorodithioate\n220-147-6\n2642-71-9\nT+; R28\nT; R24\nN; R50-53\nT+; N\nR: 24-28-50/53\nS: (1/2-)28-36/37-45-60-61\nC ≥ 25 %: T+, N; R24-28-50/53\n7 % ≤ C < 25 %: T+, N; R21-28-50/53\n3 % ≤ C < 7 %: T, N; R21-25-50/53\n1 % ≤ C < 3 %: T, N; R25-50/53\n0,25 % ≤ C < 1 %: Xn, N; R22-50/53\n0,1 % ≤ C < 0,25 %: Xn, N; R22-51/53\n0,025 % ≤ C < 0,1 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n015-067-00-1\nphosalone (ISO);\nS-(6-chloro-2-oxobenzoxazolin-3-ylmethyl) O,O-diethyl phosphorodithioate\n218-996-2\n2310-17-0\nT; R25\nXn; R20/21\nR43\nN; R50-53\nT; N\nR: 20/21-25-43-50/53\nS: (1/2-)36/37-45-60-61\nC ≥ 25 %: T, N; R21-25-50/53\n3 % ≤ C < 25 %: Xn, N; R22-50/53\n0,025 % ≤ C < 3 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n015-114-00-6\nchlormephos (ISO);\nS-chloromethyl O,O-diethyl phosphorodithioate\n246-538-1\n24934-91-6\nT+; R27/28\nN; R50-53\nT+; N\nR: 27/28-50/53\nS: (1/2-)27-28-36/37-45-60-61\nC ≥ 7 %: T+, N; R27/28-50/53\n2,5 % ≤ C < 7 %: T, N; R24/25-50/53\n1 % ≤ C < 2,5 %: T, N; R24/25-51/53\n0,25 % ≤ C < 1 %: Xn, N; R21/22-51/53\n0,1 % ≤ C < 0,25 %: Xn; R21/22-52/53\n0,025 % ≤ C < 0,1 %: R52/53\n015-115-00-1\nchlorthiophos (ISO);\n[isomeric reaction mixture in which O-2,5-dichlorophenyl-4-methylthiophenyl O,O-diethyl phosphorothioate predominates]\n244-663-6\n21923-23-9\nT+; R28\nT; R24\nN; R50-53\nT+; N\nR: 24-28-50/53\nS: (1/2-)28-36/37-45-60-61\nC ≥ 25 %: T+, N; R24-28-50/53\n7 % ≤ C < 25 %: T+, N; R21-28-50/53\n3 % ≤ C < 7 %: T, N; R21-25-50/53\n1 % ≤ C < 3 %: T, N; R25-50/53\n0,1 % ≤ C < 1 %: Xn, N; R22-50/53\n0,025 % ≤ C < 0,1 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n015-140-00-8\ntriazophos (ISO);\nO,O-diethyl-O-1-phenyl-1H-1,2,4-triazol-3-yl phosphorothioate\n245-986-5\n24017-47-8\nT; R23/25\nXn; R21\nN; R50-53\nT; N\nR: 21-23/25-50/53\nS: (1/2-)36/37-45-60-61\nC ≥ 25 %: T, N; R21-23/25-50/53\n3 % ≤ C < 25 %: Xn, N; R20/22-50/53\n0,25 % ≤ C < 3 %: N; R50/53\n0,025 % ≤ C < 0,25 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n016-084-00-7\nprosulfuron (ISO);\n1-(4-methoxy-6-methyl-1,3,5-triazin-2-yl)-3-[2-(3,3,3-trifluoropropyl)phenylsulfonyl]urea\n—\n94125-34-5\nXn; R22\nN; R50-53\nXn; N\nR: 22-50/53\nS: (2-)60-61\nC ≥ 25 %: Xn, N; R22-50/53\n0,25 % ≤ C < 25 %: N; R50/53\n0,025 % ≤ C < 0,25 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n017-001-00-7\nchlorine\n231-959-5\n7782-50-5\nT; R23\nXi; R36/37/38\nN; R50\nT; N\nR: 23-36/37/38-50\nS: (1/2-)9-45-61\nC ≥ 25 %: T, N; R23-36/37/38-50\n20 % ≤ C < 25 %: Xn, N; R20-36/37/38-50\n3 % ≤ C < 20 %: Xn, N; R20-50\n0,25 % ≤ C < 3 %: N; R50\n017-012-00-7\ncalcium hypochlorite\n231-908-7\n7778-54-3\nO; R8\nC; R34\nXn; R22\nR31\nN; R50\nO; C; N\nR: 8-22-31-34-50\nS: (1/2-)26-36/37/39-45-61\nC ≥ 25 %: C, N; R22-34-50\n10 % ≤ C < 25 %: C, N; R34-50\n3 % ≤ C < 10 %: Xi, N; R37/38-41-50\n2,5 % ≤ C < 3 %: Xi, N; R36-50\n0,5 % ≤ C < 2,5 %: Xi; R36\n017-026-00-3\nchlorine dioxide\n233-162-8\n10049-04-4\nO; R8\nR6\nT+; R26\nC; R34\nN; R50\nO; T+; N\nR: 6-8-26-34-50\nS: (1/2-)23-26-28-36/37/39-38-45-61\nC ≥ 5 %: T+, N; R26-34-50\n2,5 % ≤ C < 5 %: T+, N; R26-36/37/38-50\n1 % ≤ C < 2,5 %: T+; R26-36/37/38\n0,5 % ≤ C < 1 %: T; R23-36/37/38\n0,2 % ≤ C < 0,5 %: T; R23\n0,02 % ≤ C < 0,2 %: Xn; R20\n5\n017-026-01-0\nchlorine dioxide ... %\nB\n233-162-8\n10049-04-4\nT; R25\nC; R34\nN; R50\nT; N\nR: 25-34-50\nS: (1/2-)23-26-28-36/37/39-45-61\nC ≥ 25 %: T, N; R25-34-50\n10 % ≤ C < 25 %: C, N; R22-34-50\n3 % ≤ C < 10 %: Xn, N; R22-36/37/38-50\n2,5 % ≤ C < 3 %: Xi, N; R36-50\n0,3 % ≤ C < 2,5 %: Xi; R36\n027-004-00-5\ncobalt dichloride\nE\n231-589-4\n7646-79-9\nCarc. Cat. 2; R49\nMuta. Cat. 3; R68\nRepr. Cat. 2; R60\nXn; R22\nR42/43\nN; R50-53\nT; N\nR: 49-60-22-42/43-68-50/53\nS: 53-45-60-61\nC ≥ 25 %: T, N; R49-60-22-42/43-68-50/53\n2,5 % ≤ C < 25 %: T, N; R49-60-42/43-68-50/53\n1 % ≤ C < 2,5 %: T, N; R49-60-42/43-68-51/53\n0,5 % ≤ C < 1 %: T, N; R49-60-51/53\n0,25 % ≤ C < 0,5 %: T, N; R49-51/53\n0,025 % ≤ C < 0,25 %: T; R49-52/53\n0,01 % ≤ C < 0,025 %: T; R49\n1\n027-005-00-0\ncobalt sulfate\nE\n233-334-2\n10124-43-3\nCarc. Cat. 2; R49\nMuta. Cat. 3; R68\nRepr. Cat. 2; R60\nXn; R22\nR42/43\nN; R50-53\nT; N\nR: 49-60-22-42/43-68-50/53\nS: 53-45-60-61\nC ≥ 25 %: T, N; R49-60-22-42/43-68-50/53\n2,5 ≤ C < 25 %: T, N; R49-60-42/43-68-50/53\n1 % ≤ C < 2,5 %: T, N; R49-60-42/43-68-51/53\n0,5 % ≤ C < 1 %: T, N; R49-60-51/53\n0,25 % ≤ C < 0,5 %: T, N; R49-51/53\n0,025 % ≤ C < 0,25 %: T; R49-52/53\n0,01 % ≤ C < 0,025 %: T; R49\n1\n028-002-00-7\nnickel\nS\n231-111-4\n7440-02-0\nCarc. Cat. 3; R40\nT; R48/23\nR43\nT\nR: 40-43-48/23\nS: (2-)36/37/39-45\n7\n028-009-00-5\nnickel sulfate\nE\n232-104-9\n7786-81-4\nCarc. Cat. 1; R49\nMuta. Cat. 3; R68\nRepr. Cat. 2; R61\nT; R48/23\nXn; R20/22\nXi; R38\nR42/43\nN; R50-53\nT; N\nR: 49-61-20/22-38-42/43-48/23-68-50/53\nS: 53-45-60-61\nC ≥ 25 %: T, N; R49-61-20/22-38-42/43-48/23-68-50/53\n20 % ≤ C < 25 %: T, N; R49-61-38-42/43-48/23-68-51/53\n2,5 % ≤ C < 20 %: T, N; R49-61-42/43-48/23-68-51/53\n1 % ≤ C < 2,5 %: T; R49-61-42/43-48/23-68-52/53\n0,5 % ≤ C < 1 %: T; R49-61-43-48/20-52/53\n0,25 % ≤ C < 0,5 %: T; R49-43-48/20-52/53\n0,1 % ≤ C < 0,25 %: T; R49-43-48/20\n0,01 % ≤ C < 0,1 %: Xi; R43\n028-010-00-0\nnickel carbonate;\nbasic nickel carbonate;\ncarbonic acid, nickel (2+) salt; [1]\ncarbonic acid, nickel salt; [2]\n[μ-[carbonato(2-)-O:O’]] dihydroxy trinickel; [3]\n[carbonato(2-)] tetrahydroxytrinickel [4]\nE\n222-068-2 [1]\n240-408-8 [2]\n265-748-4 [3]\n235-715-9 [4]\n3333-67-3 [1]\n16337-84-1 [2]\n65405-96-1 [3]\n12607-70-4 [4]\nCarc. Cat. 1; R49\nMuta. Cat. 3; R68\nRepr. Cat. 2; R61\nT; R48/23\nXn; R20/22\nXi; R38\nR42/43\nN; R50-53\nT; N\nR: 49-61-20/22-38-42/43-48/23-68-50/53\nS: 53-45-60-61\n042-001-00-9\nmolybdenum trioxide\n215-204-7\n1313-27-5\nCarc. Cat. 3; R40\nXi; R36/37\nXn\nR: 36/37-40\nS: (2-)22-36/37\n042-002-00-4\ntetrakis(dimethylditetradecylammonium) hexa-μ-oxotetra-μ3-oxodi-μ5-oxotetradecaoxooctamolybdate(4-)\n404-760-8\n117342-25-3\nT; R23\nXi; R41\nT\nR: 23-41\nS: (1/2-)26-36/37/39-45\n080-006-00-8\ndimercury dicyanide oxide;\nmercuric oxycyanide\n215-629-8\n1335-31-5\nE; R2\nT; R23/24/25\nR33\nN; R50-53\nE; T; N\nR: 2-23/24/25-33-50/53\nS: (1/2-)28-36/37-45-60-61\n082-004-00-2\nlead chromate\n231-846-0\n7758-97-6\nCarc. Cat. 2; R45\nRepr. Cat. 1; R61\nRepr. Cat. 3; R62\nR33\nN; R50-53\nT; N\nR: 45-61-33-62-50/53\nS: 53-45-60-61\n1\n082-009-00-X\nlead sulfochromate yellow;\nC.I. Pigment Yellow 34;\n[This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77603.]\n215-693-7\n1344-37-2\nCarc. Cat. 2; R45\nRepr. Cat. 1; R61\nRepr. Cat. 3; R62\nR33\nN; R50-53\nT; N\nR: 45-61-33-62-50/53\nS: 53-45-60-61\n1\n082-010-00-5\nlead chromate molybdate sulfate red;\nC.I. Pigment Red 104;\n[This substance is identified in the Colour Index by Colour Index Constitution Number, C.I. 77605.]\n235-759-9\n12656-85-8\nCarc. Cat. 2; R45\nRepr. Cat. 1; R61\nRepr. Cat. 3; R62\nR33\nN; R50-53\nT; N\nR: 45-61-33-62-50/53\nS: 53-45-60-61\n1\n601-006-00-1\npentane; [1]\nisopentane;\n2-methylbutane [2]\nC\n203-692-4 [1]\n201-142-8 [2]\n109-66-0 [1]\n78-78-4 [2]\nF+; R12\nXn; R65\nR66\nR67\nN; R51-53\nF+; Xn; N\nR: 12-65-66-67-51/53\nS: (2-)9-16-29-33-61-62\n4\n601-007-00-7\nhexane (containing < 5 % n-hexane (203-777-6));\n2-methylpentane; [1]\n3-methylpentane; [2]\n2,2-dimethylbutane; [3]\n2,3-dimethylbutane [4]\nC\n203-523-4 [1]\n202-481-4 [2]\n200-906-8 [3]\n201-193-6 [4]\n107-83-5 [1]\n96-14-0 [2]\n75-83-2 [3]\n79-29-8 [4]\nF; R11\nXn; R65\nXi; R38\nR67\nN; R51-53\nF; Xn; N\nR: 11-38-65-67-51/53\nS: (2-)9-16-29-33-61-62\n4\n601-008-00-2\nheptane;\nn-heptane; [1]\n2,4-dimethylpentane; [2]\n2,2,3-trimethylbutane; [3]\n3,3-dimethylpentane; [4]\n2,3-dimethylpentane; [5]\n3-methylhexane; [6]\n2,2-dimethylpentane; [7]\n2-methylhexane; [8]\n3-ethylpentane; [9]\nisoheptane; [10]\nC\n205-563-8 [1]\n203-548-0 [2]\n207-346-3 [3]\n209-230-8 [4]\n209-280-0 [5]\n209-643-3 [6]\n209-680-5 [7]\n209-730-6 [8]\n210-529-0 [9]\n250-610-8 [10]\n142-82-5 [1]\n108-08-7 [2]\n464-06-2 [3]\n562-49-2 [4]\n565-59-3 [5]\n589-34-4 [6]\n590-35-2 [7]\n591-76-4 [8]\n617-78-7 [9]\n31394-54-4 [10]\nF; R11\nXn; R65\nXi; R38\nR67\nN; R50-53\nF; Xn; N\nR: 11-38-65-67-50/53\nS: (2-)9-16-29-33-60-61-62\n4\n601-009-00-8\noctane;\nn-octane; [1]\n2,2,4-trimethylpentane; [2]\n2,3,3-trimethylpentane; [3]\n3,3-dimethylhexane; [4]\n2,2,3-trimethylpentane; [5]\n2,3,4-trimethylpentane; [6]\n3,4-dimethylhexane; [7]\n2,3-dimethylhexane; [8]\n2,4-dimethylhexane; [9]\n4-methylheptane; [10]\n3-methylheptane; [11]\n2,2-dimethylhexane; [12]\n2,5-dimethylhexane; [13]\n2-methylheptane; [14]\n2,2,3,3-tetramethylbutane; [15]\n3-ethyl-2-methylpentane; [16]\n3-ethylhexane; [17]\n3-ethyl-3-methylpentane; [18]\nisooctane; [19]\nC\n203-892-1 [1]\n208-759-1 [2]\n209-207-2 [3]\n209-243-9 [4]\n209-266-4 [5]\n209-292-6 [6]\n209-504-7 [7]\n209-547-1 [8]\n209-649-6 [9]\n209-650-1 [10]\n209-660-6 [11]\n209-689-4 [12]\n209-745-8 [13]\n209-747-9 [14]\n209-855-6 [15]\n210-187-2 [16]\n210-621-0 [17]\n213-923-0 [18]\n247-861-0 [19]\n111-65-9 [1]\n540-84-1 [2]\n560-21-4 [3]\n563-16-6 [4]\n564-02-3 [5]\n565-75-3 [6]\n583-48-2 [7]\n584-94-1 [8]\n589-43-5 [9]\n589-53-7 [10]\n589-81-1 [11]\n590-73-8 [12]\n592-13-2 [13]\n592-27-8 [14]\n594-82-1 [15]\n609-26-7 [16]\n619-99-8 [17]\n1067-08-9 [18]\n26635-64-3 [19]\nF; R11\nXn; R65\nXi; R38\nR67\nN; R50-53\nF; Xn; N\nR: 11-38-65-67-50/53\nS: (2-)9-16-29-33-60-61-62\n4\n601-017-00-1\ncyclohexane\n203-806-2\n110-82-7\nF; R11\nXn; R65\nXi; R38\nR67\nN; R50-53\nF; Xn; N\nR: 11-38-65-67-50/53\nS: (2-)9-16-25-33-51-60-61-62\n4\n601-018-00-7\nmethylcyclohexane\n203-624-3\n108-87-2\nF; R11\nXn; R65\nXi; R38\nR67\nN; R51-53\nF; Xn; N\nR: 11-38-65-67-51/53\nS: (2-)9-16-33-61-62\n4\n601-019-00-2\n1,4-dimethylcyclohexane\n209-663-2\n589-90-2\nF; R11\nXn; R65\nXi; R38\nR67\nN; R51-53\nF; Xn; N\nR: 11-38-65-67-51/53\nS: (2-)9-16-33-61-62\n4\n601-021-00-3\ntoluene\n203-625-9\n108-88-3\nF; R11\nRepr.Cat.3; R63\nXn; R48/20-65\nXi; R38\nR67\nF; Xn\nR: 11-38-48/20-63-65-67\nS: (2-)36/37-62\n4\n601-033-00-9\nbenz[a]anthracene\n200-280-6\n56-55-3\nCarc. Cat. 2; R45\nN; R50-53\nT; N\nR: 45-50/53\nS: 53-45-60-61\nC ≥ 0,25 %: T, N; R45-50/53\n0,1 % ≤ C < 0,25 %: T, N; R45-51/53\n0,025 % ≤ C < 0,1 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n601-037-00-0\nn-hexane\n203-777-6\n110-54-3\nF; R11\nRepr. Cat. 3; R62\nXn; R48/20-65\nXi; R38\nR67\nN; R51-53\nF; Xn; N\nR: 11-38-48/20-62-65-67-51/53\nS: (2-)9-16-29-33-36/37-61-62\nC ≥ 25 %: Xn, N; R38-48/20-62-51/53\n20 % ≤ C < 25 %: Xn; R38-48/20-62-52/53\n5 % ≤ C < 20 %: Xn; R48/20-62-52/53\n2,5 % ≤ C < 5 %: R52/53\n4\n601-041-00-2\ndibenz[a,h]anthracene\n200-181-8\n53-70-3\nCarc. Cat. 2; R45\nN; R50-53\nT; N\nR: 45-50/53\nS: 53-45-60-61\nC ≥ 0,25 %: T, N; R45-50/53\n0,025 % ≤ C < 0,25 %: T, N; R45-51/53\n0,01 % ≤ C < 0,025 %: T; R45-52/53\n0,0025 % ≤ C < 0,01 %: R52/53\n602-050-00-4\nisodrin;\n(1α,4α,4aβ,5β,8β,8aβ)-1,2,3,4,10,10-hexachloro-1,4,4a,5,8,8a-hexahydro-1,4:5,8-dimethanonaphthalene\n207-366-2\n465-73-6\nT+; R26/27/28\nN; R50-53\nT+; N\nR: 26/27/28-50/53\nS: (1/2-)13-28-36/37-45-60-61\nC ≥ 7 %: T+, N; R26/27/28-50/53\n1 % ≤ C < 7 %: T, N; R23/24/25-50/53\n0,25 % ≤ C < 1 %: Xn, N; R20/21/22-50/53\n0,1 % ≤ C < 0,25 %: Xn, N; R20/21/22-51/53\n0,025 % ≤ C < 0,1 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n602-052-00-5\nendosulfan (ISO);\n1,2,3,4,7,7-hexachloro-8,9,10-trinorborn-2-en-5,6-ylenedimethyl sulfite;\n1,4,5,6,7,7-hexachloro-8,9,10-trinorborn-5-en-2,3-ylenedimethylene) sulfite\n204-079-4\n115-29-7\nT+; R26/28\nXn; R21\nN; R50-53\nT+; N\nR: 21-26/28-50/53\nS: (1/2-)28-36/37-45-60-61-63\n602-076-00-6\n2,3,4-trichlorobut-1-ene\n219-397-9\n2431-50-7\nCarc. Cat. 3; R40\nT; R23\nXn; R22\nXi; R36/37/38\nN; R50-53\nT; N\nR: 22-23-36/37/38-40-50/53\nS: (1/2-)36/37-45-60-61\nC ≥ 25 %: T, N; R22-23-36/37/38-40-50/53\n20 % ≤ C < 25 %: Xn, N; R20-36/37/38-40-51/53\n3 % ≤ C < 20 %: Xn, N; R20-40-51/53\n2,5 % ≤ C < 3 %: Xn, N; R40-51/53\n0,25 % ≤ C < 2,5 %: Xn; R40-52/53\n0,1 % ≤ C < 0,25 %: Xn; R40\n602-080-00-8\nalkanes, C10-13, chloro;\nchlorinated paraffins, C10-13\n287-476-5\n85535-84-8\nCarc. Cat. 3; R40\nR66\nN; R50-53\nXn; N\nR: 40-66-50/53\nS: (2-)24-36/37-46-60-61\n603-003-00-0\npropan-1-ol;\nn-propanol\n200-746-9\n71-23-8\nF; R11\nXi; R41\nR67\nF; Xi\nR: 11-41-67\nS: (2-)7-16-24-26-39\n603-004-00-6\nbutan-1-ol;\nn-butanol\n200-751-6\n71-36-3\nR10\nXn; R22\nXi; R37/38-41\nR67\nXn\nR: 10-22-37/38-41-67\nS: (2-)7/9-13-26-37/39-46\n603-022-00-4\ndiethyl ether;\nether\n200-467-2\n60-29-7\nF+; R12\nR19\nXn; R22\nR66\nR67\nF+; Xn\nR: 12-19-22-66-67\nS: (2-)9-16-29-33\n603-032-00-9\nethylene dinitrate;\nethylene glycol dinitrate\n211-063-0\n628-96-6\nE; R3\nT+; R26/27/28\nR33\nE; T+\nR: 3-26/27/28-33\nS: (1/2-)27/28-33-35-36/37-45\n603-037-00-6\ncellulose nitrate;\nnitrocellulose, containing more than 12,6 % nitrogen\n—\n—\nE; R3\nE\nR: 3\nS: (2-)35\n603-045-00-X\ndiisopropyl ether; [1]\ndipropyl ether [2]\nC\n203-560-6 [1]\n203-869-6 [2]\n108-20-3 [1]\n111-43-3 [2]\nF; R11\nR19\nR66\nR67\nF\nR: 11-19-66-67\nS: (2-)9-16-29-33\n603-085-00-8\nbronopol (INN);\n2-bromo-2-nitropropane-1,3-diol\n200-143-0\n52-51-7\nXn; R21/22\nXi; R37/38-41\nN; R50\nXn; N\nR: 21/22-37/38-41-50\nS: (2-)26-36/37/39-61\nC ≥ 25 %: Xn, N; R21/22-37/38-41-50\n20 % ≤ C < 25 %: Xi, N; R37/38-41-50\n10 % ≤ C < 20 %: Xi, N; R41-50\n5 % ≤ C < 10 %: Xi, N; R36-50\n2,5 % ≤ C < 5 %: N; R50\n603-108-00-1\n2-methylpropan-1-ol;\niso-butanol\n201-148-0\n78-83-1\nR10\nXi; R37/38-41\nR67\nXi\nR: 10-37/38-41-67\nS: (2-)7/9-13-26-37/39-46\n603-117-00-0\npropan-2-ol;\nisopropyl alcohol;\nisopropanol\n200-661-7\n67-63-0\nF; R11\nXi; R36\nR67\nF; Xi\nR: 11-36-67\nS: (2-)7-16-24/25-26\n603-127-00-5\nbutan-2-ol; [1]\n(S)-butan-2-ol; [2]\n(R)-butan-2-ol; [3]\n(±)-butan-2-ol [4]\nC\n201-158-5 [1]\n224-168-1 [2]\n238-967-8 [3]\n240-029-8 [4]\n78-92-2 [1]\n4221-99-2 [2]\n14898-79-4 [3]\n15892-23-6 [4]\nR10\nXi; R36/37\nR67\nXi\nR: 10-36/37-67\nS: (2-)7/9-13-24/25-26-46\n604-005-00-4\n1,4-dihydroxybenzene;\nhydroquinone;\nquinol\n204-617-8\n123-31-9\nCarc. Cat. 3; R40\nMuta. Cat. 3; R68\nXn; R22\nXi; R41\nR43\nN; R50\nXn; N\nR: 22-40-41-43-68-50\nS: (2-)26-36/37/39-61\nC ≥ 25 %: Xn, N; R22-40-41-43-68-50\n10 % ≤ C < 25 %: Xn, N; R40-41-43-68-50\n5 % ≤ C < 10 %: Xn, N; R36-40-43-68-50\n2,5 % ≤ C < 5 %: Xn, N; R40-43-68-50\n1 % ≤ C < 2,5 %: Xn; R40-43-68\n604-030-00-0\nbisphenol A;\n4,4'-isopropylidenediphenol\n201-245-8\n80-05-7\nRepr. Cat. 3; R62\nXi; R37-41\nR43\nR52\nXn\nR: 37-41-43-62-52\nS: (2-)26-36/37-39-46-61\n604-055-00-7\n2,2'-((3,3',5,5'-tetramethyl-(1,1'-biphenyl)-4,4'-diyl)-bis(oxymethylene))-bis-oxirane\n413-900-7\n85954-11-6\nCarc. Cat. 3; R40\nR43\nXn\nR: 40-43\nS: (2-)22-36/37\n605-010-00-4\n2-furaldehyde\n202-627-7\n98-01-1\nCarc. Cat. 3; R40\nT; R23/25\nXn; R21\nXi; R36/37/38\nT\nR: 21-23/25-36/37/38-40\nS: (1/2-)26-36/37-45\n606-001-00-8\nacetone;\npropan-2-one;\npropanone\n200-662-2\n67-64-1\nF; R11\nXi; R36\nR66\nR67\nF; Xi\nR: 11-36-66-67\nS: (2-)9-16-26-46\n606-002-00-3\nbutanone;\nethyl methyl ketone\n201-159-0\n78-93-3\nF; R11\nXi; R36\nR66\nR67\nF; Xi\nR: 11-36-66-67\nS: (2-)9-16\n606-006-00-5\npentan-3-one;\ndiethyl ketone\n202-490-3\n96-22-0\nF; R11\nXi; R37\nR66\nR67\nF; Xi\nR: 11-37-66-67\nS: (2-)9-16-25-33\n606-013-00-3\np-benzoquinone;\nquinone\n203-405-2\n106-51-4\nT; R23/25\nXi; R36/37/38\nN; R50\nT; N\nR: 23/25-36/37/38-50\nS: (1/2-)26-28-45-61\nC ≥ 25 %: T, N; R23/25-36/37/38-50\n20 % ≤ C < 25 %: Xn, N; R20/22-36/37/38-50\n3 % ≤ C < 20 %: Xn, N; R20/22-50\n2,5 % ≤ C < 3 %: N; R50\n606-030-00-6\nhexan-2-one;\nmethyl butyl ketone;\nbutyl methyl ketone;\nmethyl-n-butyl ketone\n209-731-1\n591-78-6\nR10\nRepr. Cat. 3; R62\nT; R48/23\nR67\nT\nR: 10-48/23-62-67\nS: (1/2-)36/37-45\nC ≥ 10 %: T; R48/23-62\n5 % ≤ C < 10 %: Xn; R48/20-62\n1 % ≤ C < 5 %: Xn; R48/20\n606-034-00-8\nmetribuzin (ISO);\n4-amino-6-tert-butyl-3-methylthio-1,2,4-triazin-5(4H)-one;\n4-amino-4,5-dihydro-6-(1,1-dimethylethyl)-3-methylthio-1,2,4-triazin-5-one\n244-209-7\n21087-64-9\nXn; R22\nN; R50-53\nXn; N\nR: 22-50/53\nS: (2-)60-61\nC ≥ 25 %: Xn, N; R22-50/53\n2,5 % ≤ C < 25 %: N; R50/53\n0,25 % ≤ C < 2,5 %: N; R51/53\n0,025 % ≤ C < 0,25 %: R52/53\n607-003-00-1\nchloroacetic acid\n201-178-4\n79-11-8\nT; R23/24/25\nC; R34\nN; R50\nT; N\nR: 23/24/25-34-50\nS: (1/2-)26-36/37/39-45-61-63\nC ≥ 25 %: T, N; R23/24/25-34-50\n10 % ≤ C < 25 %: C; R20/21/22-34\n5 % ≤ C < 10 %: Xn; R20/21/22-36/37/38\n3 % ≤ C < 5 %: Xn; R20/21/22\n607-016-00-2\npropyl formate; [1]\nisopropyl formate [2]\nC\n203-798-0 [1]\n210-901-2 [2]\n110-74-7 [1]\n625-55-8 [2]\nF; R11\nXi; R36/37\nR67\nF; Xi\nR: 11-36/37-67\nS: (2-)9-16-24-33\n607-021-00-X\nmethyl acetate\n201-185-2\n79-20-9\nF; R11\nXi; R36\nR66\nR67\nF; Xi\nR: 11-36-66-67\nS: (2-)16-26-29-33\n607-022-00-5\nethyl acetate\n205-500-4\n141-78-6\nF; R11\nXi; R36\nR66\nR67\nF; Xi\nR: 11-36-66-67\nS: (2-)16-26-33\n607-024-00-6\npropyl acetate; [1]\nisopropyl acetate [2]\nC\n203-686-1 [1]\n203-561-1 [2]\n109-60-4 [1]\n108-21-4 [2]\nF; R11\nXi; R36\nR66\nR67\nF; Xi\nR: 11-36-66-67\nS: (2-)16-26-29-33\n607-025-00-1\nn-butyl acetate\n204-658-1\n123-86-4\nR10\nR66\nR67\nR: 10-66-67\nS: (2-)25\n607-065-00-X\nbromoacetic acid\n201-175-8\n79-08-3\nT; R23/24/25\nC; R35\nR43\nN; R50\nT; C; N\nR: 23/24/25-35-43-50\nS: (1/2-)26-36/37/39-45-61\n607-162-00-7\ndalapon;\n2,2-dichloropropionic acid; [1]\ndalapon-sodium;\nsodium 2,2-dichloropropionate [2]\n200-923-0 [1]\n204-828-5 [2]\n75-99-0 [1]\n127-20-8 [2]\nXi; R38-41\nR52-53\nXi\nR: 38-41-52/53\nS: (2-)26-39-61\n607-189-00-4\ntrimethylenediaminetetraacetic acid\n400-400-9\n1939-36-2\nXn; R22\nXi; R41\nXn\nR: 22-41\nS: (2-)22-26-39\n607-213-00-3\nethyl 3,3-bis(tert-pentylperoxy)butyrate\n403-320-2\n67567-23-1\nE; R3\nO; R7\nR10\nN; R51-53\nE; N\nR: 3-7-10-51/53\nS: (2-)3/7-14-33-36/37/39-61\n607-252-00-6\nlambda-cyhalothrin (ISO);\nA 1:1 mixture of: (S)-α-cyano-3-phenoxybenzyl(Z)-(1R)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate;\n(R)-α-cyano-3-phenoxybenzyl (Z)-(1S)-cis-3-(2-chloro-3,3,3-trifluoropropenyl)-2,2-dimethylcyclopropanecarboxylate\n415-130-7\n91465-08-6\nT+; R26\nT; R25\nXn; R21\nN; R50-53\nT+; N\nR: 21-25-26-50/53\nS: (1/2-)28-36/37/39-38-45-60-61\nC ≥ 25 %: T+, N; R21-25-26-50/53\n7 % ≤ C < 25 %: T+, N; R22-26-50/53\n3 % ≤ C < 7 %: T, N; R22-23-50/53\n1 % ≤ C < 3 %: T, N; R23-50/53\n0,1 % ≤ C < 1 %: Xn, N; R20-50/53\n0,0025 % ≤ C < 0,1 %: N; R50/53\n0,00025 % ≤ C < 0,0025 %: N; R51/53\n0,000025 % ≤ C < 0,00025 %: R52/53\n607-253-00-1\ncyfluthrin (ISO);\nα-cyano-4-fluoro-3-phenoxybenzyl-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate\n269-855-7\n68359-37-5\nT+; R28\nT; R23\nN; R50-53\nT+; N\nR: 23-28-50/53\nS: (1/2-)28-36/37/39-45-60-61\nC ≥ 25 %: T+, N; R23-28-50/53\n7 % ≤ C < 25 %: T+, N; R20-28-50/53\n3 % ≤ C < 7 %: T, N; R20-25-50/53\n1 % ≤ C < 3 %: T, N; R25-50/53\n0,1 % ≤ C < 1 %: Xn, N; R22-50/53\n0,025 % ≤ C < 0,1 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n607-319-00-X\ndeltamethrin (ISO);\n(S)-α-cyano-3-phenoxybenzyl (1R, 3R)-3-(2,2-dibromovinyl)-2,2-dimethylcyclopropanecarboxylate\n258-256-6\n52918-63-5\nT; R23/25\nN; R50-53\nT; N\nR: 23/25-50/53\nS: (1/2-)24-28-36/37/39-38-45-60-61\nC ≥ 25 %: T, N; R23/25-50/53\n3 % ≤ C < 25 %: Xn, N; R20/22-50/53\n0,000025 % ≤ C < 3 %: N; R50/53\n0,0000025 % ≤ C < 0,000025 %: N; R51/53\n0,00000025 % ≤ C < 0,0000025 %: R52/53\n607-422-00-X\nα-cypermethrin (ISO);\nracemate comprising (R)-α-cyano-3-phenoxybenzyl (1S,3S)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate;\n(S)-α-cyano-3-phenoxybenzyl (1R,3R)-3-(2,2-dichlorovinyl)-2,2-dimethylcyclopropanecarboxylate\n257-842-9\n67375-30-8\nT; R25\nXn; R48/22\nXi; R37\nN; R50-53\nT; N\nR: 25-37-48/22-50/53\nS: (1/2-)36/37/39-45-60-61\nC ≥ 25 %: T, N; R25-37-48/22-50/53\n20 % ≤ C < 25 %: Xn, N; R22-37-48/22-50/53\n10 % ≤ C < 20 %: Xn, N; R22-48/22-50/53\n3 % ≤ C < 10 %: Xn, N; R22-50/53\n0,025 % ≤ C < 3 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n608-014-00-4\nchlorothalonil (ISO);\ntetrachloroisophthalonitrile\n217-588-1\n1897-45-6\nCarc. Cat. 3; R40\nT+; R26\nXi; R37-41\nR43\nN; R50-53\nT+; N\nR: 26-37-40-41-43-50/53\nS: (1/2-)28-36/37/39-45-60-61\nC ≥ 20 %: T+, N; R26-37-40-41-43-50/53\n10 % ≤ C < 20 %: T+, N; R26-40-41-43-50/53\n7 % ≤ C < 10 %: T+, N; R26-40-36-43-50/53\n5 % ≤ C < 7 %: T, N; R23-40-36-43-50/53\n2,5 % ≤ C < 5 %: T, N; R23-40-43-50/53\n1 % ≤ C < 2,5 %: T, N; R23-40-43-51/53\n0,25 % ≤ C < 1 %: Xn, N; R20-51/53\n0,1 % ≤ C < 0,25 %: Xn; R20-52/53\n0,025 % ≤ C < 0,1 %: R52/53\n608-034-00-3\nchlorfenapyr (ISO);\n4-bromo-2-(4-chlorophenyl)-1-ethoxymethyl-5-trifluoromethylpyrrole-3-carbonitrile\n—\n122453-73-0\nT; R23\nXn; R22\nN; R50-53\nT; N\nR: 22-23-50/53\nS: (1/2-)13-36/37-45-60-61\nC ≥ 25 %: T, N; R23-22-50/53\n3 % ≤ C < 25 %: Xn, N; R20-50/53\n0,25 % ≤ C < 3 %: N; R50/53\n0,025 % ≤ C < 0,25 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n608-058-00-4\nesfenvalerate (ISO);\n(S)-α-cyano-3-phenoxybenzyl-(S)-2-(4-chlorophenyl)-3-methylbutyrate\n—\n66230-04-4\nT; R23/25\nR43\nN; R50-53\nT; N\nR: 23/25-43-50/53\nS: (1/2-)24-36/37/39-45-60-61\nC ≥ 25 %: T, N; R23/25-43-50/53\n3 % ≤ C < 25 %: Xn, N; R20/22-43-50/53\n1 % ≤ C < 3 %: Xi, N; R43-50/53\n0,0025 % ≤ C < 1 %: N; R50/53\n0,00025 % ≤ C < 0,0025 %: N; R51/53\n0,000025 % ≤ C < 0,00025 %: R52/53\n609-005-00-8\n1,3,5-trinitrobenzene\n202-752-7\n99-35-4\nE; R3\nT+; R26/27/28\nR33\nN; R50-53\nE; T+; N\nR: 3-26/27/28-33-50/53\nS: (1/2-)28-36/37-45-60-61\n609-009-00-X\n2,4,6-trinitrophenol;\npicric acid\n201-865-9\n88-89-1\nE; R3\nR4\nT; R23/24/25\nE; T\nR: 3-4-23/24/25\nS: (1/2-)28-35-36/37-45\n609-018-00-9\n2,4,6-trinitroresorcinol;\nstyphnic acid\n201-436-6\n82-71-3\nE; R3\nR4\nXn; R20/21/22\nE; Xn\nR: 3-4-20/21/22\nS: (2-)35-36/37\n609-023-00-6\ndinocap (ISO);\n(RS)-2,6-dinitro-4-octylphenyl crotonates and (RS)-2,4-dinitro-6-octylphenyl crotonates in which “octyl” is a mixture of 1-methylheptyl, 1-ethylhexyl and 1-propylpentyl groups\nE\n254-408-0\n39300-45-3\nRepr. Cat. 2; R61\nXn; R20/22-48/22\nXi; R38\nR43\nN; R50-53\nT; N\nR: 61-20/22-38-43-48/22-50/53\nS: 53-45-60-61\nC ≥ 25 %: T, N; R61-20/22-38-43-48/22-50/53\n20 % ≤ C < 25 %: T, N; R61-38-43-48/22-50/53\n10 % ≤ C < 20 %: T, N; R61-43-48/22-50/53\n1 % ≤ C < 10 %: T, N; R61-43-50/53\n0,5 % ≤ C < 1 %: T, N; R61-50/53\n0,25 % ≤ C < 0,5 %: N; R50/53\n0,025 % ≤ C < 0,25 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n609-046-00-1\ntrifluralin (ISO) (containing < 0.5 ppm NPDA);\nα,α,α-trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine (containing < 0.5 ppm NPDA);\n2,6-dinitro-N,N-dipropyl-4-trifluoromethylaniline (containing < 0.5 ppm NPDA);\nN,N-dipropyl-2,6-dinitro-4-trifluoromethylaniline (containing < 0.5 ppm NPDA)\n216-428-8\n1582-09-8\nCarc. Cat. 3; R40\nR43\nN; R50-53\nXn; N\nR: 40-43-50/53\nS: (2-)36/37-46-60-61\nC ≥ 2,5 %: Xn, N; R40-43-50/53\n1 % ≤ C < 2,5 %: Xn, N; R40-43-51/53\n0,25 % ≤ C < 1 %: N; R51/53\n0,025 % ≤ C < 0,25 %: R52/53\n611-067-00-6\nA mixture of: bis(tris(2-(2-hydroxy(1-methyl)ethoxy)ethyl)ammonium) 7-anilino-4-hydroxy-3-(2-methoxy-5-methyl-4-(4-sulfonatophenylazo)phenylazo)naphthalene-2-sulfonate;\nbis(tris(2-(2-hydroxy(2-methyl)ethoxy)ethyl)ammonium) 7-anilino-4-hydroxy-3-(2-methoxy-5-methyl-4-(4-sulfonatophenylazo)phenylazo)naphthalene-2-sulfonate\n406-910-8\n—\nXn; R22\nR52-53\nXn\nR: 22-52/53\nS: (2-)22-61\n611-130-00-8\ntetra-ammonium 2-[6-[7-(2-carboxylato-phenylazo)-8-hydroxy-3,6-disulfonato-1-naphthylamino]-4-hydroxy-1,3,5-triazin-2-ylamino]benzoate\n418-520-5\n183130-96-3\nXi; R36\nR52-53\nXi\nR: 36-52/53\nS: (2-)26-39-61\n612-017-00-6\nN-methyl-N-2,4,6-tetranitroaniline;\ntetryl\n207-531-9\n479-45-8\nE; R3\nT; R23/24/25\nR33\nE; T\nR: 3-23/24/25-33\nS: (1/2-)35-36/37-45-63\n612-018-00-1\nbis(2,4,6-trinitrophenyl)amine;\nhexyl\n205-037-8\n131-73-7\nE; R3\nT+; R26/27/28\nR33\nN; R51-53\nE; T+; N\nR: 3-26/27/28-33-51/53\nS: (1/2-)27/28-35-36/37-45-61-63\n612-019-00-7\ndipicrylamine, ammonium salt\n220-639-0\n2844-92-0\nE; R3\nT+; R26/27/28\nR33\nN; R51-53\nE; T+; N\nR: 3-26/27/28-33-51/53\nS: (1/2-)27/28-36/37-45-61-63\n612-034-00-9\n2-amino-4,6-dinitrophenol;\npicramic acid\n202-544-6\n96-91-3\nE; R2\nXn; R20/21/22\nR52-53\nE; Xn\nR: 2-20/21/22-52/53\nS: (2-)35-36/37-46-61\n612-057-00-4\npiperazine;\n[solid]\n203-808-3\n110-85-0\nRepr. Cat. 3; R62-63\nC; R34\nR42/43\nXn; C\nR: 34-42/43-62-63\nS: (1/2-)22-26-36/37/39-45\n612-083-00-6\n1-methyl-3-nitro-1-nitrosoguanidine\nE\n200-730-1\n70-25-7\nCarc. Cat. 2; R45\nXn; R20\nXi; R36/38\nN; R51-53\nT; N\nR: 45-20-36/38-51/53\nS: 53-45-61\nC ≥ 25 %: T, N; R45-20-36/38-51/53\n20 % ≤ C < 25 %: T; R45-36/38-52/53\n2,5 % ≤ C < 20 %: T; R45-52/53\n0,01 % ≤ C < 2,5 %: T; R45\n612-094-00-6\n4-(2-chloro-4-trifluoromethyl)phenoxy-2-fluoroaniline hydrochloride\n402-190-4\n113674-95-6\nT; R48/25\nXn; R22-48/20\nXi; R41\nR43\nN; R50-53\nT; N\nR: 22-41-43-48/20-48/25-50/53\nS: (1/2-)26-36/37/39-45-60-61\n612-098-00-8\nnitrosodipropylamine\nE\n210-698-0\n621-64-7\nCarc. Cat. 2; R45\nXn; R22\nN; R51-53\nT; N\nR: 45-22-51/53\nS: 53-45-61\nC ≥ 25 %: T, N; R45-22-51/53\n2,5 % ≤ C < 25 %: T; R45-52/53\n0,001 % ≤ C < 2,5 %: T; R45\n612-122-00-7\nhydroxylamine .... %\n[> 55 % in aqueous solution]\nB\n232-259-2\n7803-49-8\nE; R2\nCarc. Cat. 3; R40\nXn; R21/22-48/22\nXi; R37/38-41\nR43\nN; R50\nE; Xn; N\nR: 2-21/22-37/38-40-41-43-48/22-50\nS: (2-)26-36/37/39-61\n612-123-00-2\nhydroxylammonium chloride;\nhydroxylamine hydrochloride; [1]\nbis(hydroxylammonium) sulfate;\nhydroxylamine sulfate (2:1) [2]\n226-798-2 [1]\n233-118-8 [2]\n5470-11-1 [1]\n10039-54-0 [2]\nE; R2\nCarc. Cat. 3; R40\nXn; R21/22-48/22\nXi; R36/38\nR43\nN; R50\nE; Xn; N\nR: 2-21/22-36/38-40-43-48/22-50\nS: (2-)36/37-61\n613-003-00-2\n1,2,3,4-tetranitrocarbazole\n—\n6202-15-9\nE; R2\nXn; R20/21/22\nE; Xn\nR: 2-20/21/22\nS: (2-)35-36/37\n613-010-00-0\nametryn (ISO);\n2-ethylamino-4-isopropylamino-6-methylthio-1,3,5-triazine\n212-634-7\n834-12-8\nXn; R22\nN; R50-53\nXn; N\nR: 22-50/53\nS: (2-)36-60-61\nC ≥ 25 %: Xn, N; R22-50/53\n0,25 % ≤ C < 25 %: N; R50/53\n0,025 % ≤ C < 0,25 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n613-030-00-X\ntroclosene potassium; [1]\ntroclosene sodium [2]\nT\n218-828-8 [1]\n220-767-7 [2]\n2244-21-5 [1]\n2893-78-9 [2]\nE; R2\nO; R8\nXn; R22\nXi; R36/37\nR31\nN; R50-53\nE; Xn; N\nR: 2-8-22-31-36/37-50/53\nS: (2-)8-26-41-45-60-61\nC ≥ 25 %: Xn, N; R22-36/37-50/53\n10 % ≤ C < 25 %: Xn, N; R22-31-36/37-51/53\n2,5 % ≤ C < 10 %: N; R51/53\n0,25 % ≤ C < 2,5 %: R52/53\n613-044-00-6\ncaptan (ISO);\n1,2,3,6-tetrahydro-N-(trichloromethylthio)phthalimide\n205-087-0\n133-06-2\nCarc. Cat. 3; R40\nT; R23\nXi; R41\nR43\nN; R50\nT; N\nR: 23-40-41-43-50\nS: (1/2-)26-29-36/37/39-45-61\nC ≥ 25 %: T, N; R23-40-41-43-50\n10 % ≤ C < 25 %: Xn, N; R20-40-41-43-50\n5 % ≤ C < 10 %: Xn, N; R20-36-40-43-50\n3 % ≤ C < 5 %: Xn, N; R20-40-43-50\n2,5 % ≤ C < 3 %: Xn, N; R40-43-50\n1 % ≤ C < 2,5 %: Xn; R40-43\n613-045-00-1\nfolpet (ISO);\nN-(trichloromethylthio)phthalimide\n205-088-6\n133-07-3\nCarc. Cat. 3; R40\nXn; R20\nXi; R36\nR43\nN; R50\nXn; N\nR: 20-36-40-43-50\nS: (2-)36/37-46-61\nC ≥ 25 %: Xn, N; R20-36-40-43-50\n20 % ≤ C < 25 %: Xn, N; R36-40-43-50\n2,5 % ≤ C < 20 %: Xn, N; R40-43-50\n1 % ≤ C < 2,5 %: Xn; R40-43\n613-060-00-3\nresmethrin (ISO);\n5-benzyl-3-furylmethyl (±)-cis-trans-chrysanthemate\n233-940-7\n10453-86-8\nXn; R22\nN; R50-53\nXn; N\nR: 22-50/53\nS: (2-)60-61\nC ≥ 25 %: Xn, N; R22-50/53\n0,025 % ≤ C < 25 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n613-120-00-9\nbioresmethrin (ISO);\n(5-benzylfur-3-yl)methyl(1R)-trans-2,2-dimethyl-3-(2-methylpropenyl)cyclopropanecarboxylate\n249-014-0\n28434-01-7\nN; R50-53\nN\nR: 50/53\nS: 60-61\nC ≥ 0,025 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n613-139-00-2\nmetsulfuron-methyl (ISO);\n2-(4-methoxy-6-methyl-1,3,5-triazin-2-ylcarbamoylsulfamoyl) benzoic acid\n—\n74223-64-6\nN; R50-53\nN\nR: 50/53\nS: 60-61\nC ≥ 0,025 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n613-163-00-3\nazimsulfuron (ISO);\n1-(4,6-dimethoxypyrimidin-2-yl)-3-[1-methyl-4-(2-methyl-2H-tetrazol-5-yl)pyrazol-5-ylsulfonyl]urea\n—\n120162-55-2\nN; R50-53\nN\nR: 50/53\nS: 60-61\nC ≥ 0,025 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n613-164-00-9\nflufenacet (ISO);\nN-(4-fluorophenyl)-N-isopropyl-2-(5-trifluoromethyl-[1,3,4]thiadiazol-2-yloxy)acetamide\n—\n142459-58-3\nXn; R22-48/22\nR43\nN; R50-53\nXn; N\nR: 22-43-48/22-50/53\nS: (2-)13-24-37-60-61\nC ≥ 25 %: Xn, N; R22-43-48/22-50/53\n10 % ≤ C < 25 %: Xn, N; R43-48/22-50/53\n1 % ≤ C < 10 %: Xi, N; R43-50/53\n0,25 % ≤ C < 1 %: N; R50/53\n0,025 % ≤ C < 0,25 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n613-165-00-4\nflupyrsulfuron-methyl-sodium (ISO);\nmethyl 2-[[(4,6-dimethoxypyrimidin-2-ylcarbamoyl)sulfamoyl]-6-trifluoromethyl]nicotinate, monosodium salt\n—\n144740-54-5\nN; R50-53\nN\nR: 50/53\nS: 60-61\nC ≥ 0,25 %: N; R50/53\n0,025 % ≤ C < 0,25 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n613-166-00-X\nflumioxazin (ISO);\nN-(7-fluoro-3,4-dihydro-3-oxo-4-prop-2-ynyl-2H-1,4-benzoxazin-6-yl)cyclohex-1-ene-1,2-dicarboxamide\n—\n103361-09-7\nRepr. Cat. 2; R61\nN; R50-53\nT; N\nR: 61-50/53\nS: 53-45-60-61\nC ≥ 0,5 %: T, N; R61-50/53\n0,025 % ≤ C < 0,5 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n613-169-00-6\n9-vinylcarbazole\n216-055-0\n1484-13-5\nMuta. Cat. 3; R68\nXn; R21/22\nXi; R38\nR43\nN; R50-53\nXn; N\nR: 21/22-38-43-68-50/53\nS: (2-)22-23-36/37-60-61\nC ≥ 25 %: Xn, N; R21/22-38-43-68-50/53\n20 % ≤ C < 25 %: Xn, N; R38-43-68-50/53\n1 % ≤ C < 20 %: Xn, N; R43-68-50/53\n0,25 % ≤ C < 1 %: N; R50/53\n0,025 % ≤ C < 0,25 %: N; R51/53\n0,0025 % ≤ C < 0,025 %: R52/53\n613-174-00-3\ntetraconazole (ISO);\n(+/-) 2-(2,4-dichlorophenyl)-3-(1H-1,2,4-triazol-1-yl)propyl-1,1,2,2-tetrafluoroethylether\n407-760-6\n112281-77-3\nXn; R20/22\nN; R51-53\nXn; N\nR: 20/22-51/53\nS: (2-)36-61\n613-203-00-X\npyraflufen-ethyl (ISO);\n2-chloro-5-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)-4-fluorophenoxyacetic acid ethyl ester; [1]\npyraflufen (ISO);\n2-chloro-5-(4-chloro-5-difluoromethoxy-1-methylpyrazol-3-yl)-4-fluorophenoxyacetic acid [2]\n[1]\n[2]\n129630-19-9 [1]\n129630-17-7 [2]\nN; R50-53\nN\nR: 50/53\nS: 60-61\nC ≥ 0,025 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n613-204-00-5\noxadiargyl (ISO);\n3-[2,4-dichloro-5-(2-propynyloxy)phenyl]-5-(1,1-dimethylethyl)-1,3,4-oxadiazol-2(3H)-one;\n5-tert-butyl-3-[2,4-dichloro-5-(prop-2-ynyloxy)phenyl]-1,3,4-oxadiazol-2(3H)-one\n254-637-6\n39807-15-3\nRepr. Cat. 3; R63\nXn; R48/22\nN; R50-53\nXn; N\nR: 48/22-63-50/53\nS: (2-)36/37-46-60-61\nC ≥ 10 %: Xn, N; R48/22-63-50/53\n5 % ≤ C < 10 %: Xn, N; R63-50/53\n0,025 % ≤ C < 5 %: N; R50/53\n0,0025 % ≤ C < 0,025 %: N; R51/53\n0,00025 % ≤ C < 0,0025 %: R52/53\n614-005-00-6\ncolchicine\nE\n200-598-5\n64-86-8\nMuta. Cat. 2; R46\nT+; R28\nT+\nR: 46-28\nS: 53-45\n615-005-00-9\n4,4'-methylenediphenyl diisocyanate;\ndiphenylmethane-4,4'-diisocyanate; [1]\n2,2'-methylenediphenyl diisocyanate;\ndiphenylmethane-2,2'-diisocyanate; [2]\no-(p-isocyanatobenzyl)phenyl isocyanate;\ndiphenylmethane-2,4'-diisocyanate; [3]\nmethylenediphenyl diisocyanate [4]\nC\n202-966-0 [1]\n219-799-4 [2]\n227-534-9 [3]\n247-714-0 [4]\n101-68-8 [1]\n2536-05-2 [2]\n5873-54-1 [3]\n26447-40-5 [4]\nCarc. Cat. 3; R40\nXn; R20-48/20\nXi; R36/37/38\nR42/43\nXn\nR: 20-36/37/38-40-42/43-48/20\nS: (1/2-)23-36/37-45\nC ≥ 25 %: Xn; R20-36/37/38-40-42/43-48/20\n10 % ≤ C < 25 %: Xn; R36/37/38-40-42/43-48/20\n5 % ≤ C < 10 %: Xn; R36/37/38-40-42/43\n1 % ≤ C < 5 %: Xn; R40-42/43\n0,1 % ≤ C < 1 %: Xn; R42\n2\n615-022-00-1\nmethyl 3-isocyanatosulfonyl-2-thiophene-carboxylate\n410-550-7\n79277-18-2\nR14\nXn; R48/22\nR42/43\nXn\nR: 14-42/43-48/22\nS: (2-)22-30-35-36/37-45\n616-006-00-7\ndichlofluanid (ISO);\nN-dichlorofluoromethylthio-N',N'-dimethyl-N-phenylsulfamide\n214-118-7\n1085-98-9\nXn; R20\nXi; R36\nR43\nN; R50\nXn; N\nR: 20-36-43-50\nS: (2-)24-37-61\nC ≥ 25 %: Xn, N; R20-36-43-50\n20 % ≤ C < 25 %: Xi, N; R36-43-50\n2,5 % ≤ C < 20 %: Xi, N; R43-50\n1 % ≤ C < 2,5 %: Xi; R43\n616-009-00-3\npropanil (ISO);\n3',4'-dichloropropionanilide\n211-914-6\n709-98-8\nXn; R22\nN; R50\nXn; N\nR: 22-50\nS: (2-)22-61\nC ≥ 25 %: Xn, N; R22-50\n2,5 % ≤ C < 25 %: N; R50\n617-008-00-0\ndibenzoyl peroxide;\nbenzoyl peroxide\n202-327-6\n94-36-0\nE; R3\nO; R7\nXi; R36\nR43\nE; Xi\nR: 3-7-36-43\nS: (2-)3/7-14-36/37/39\n617-010-00-1\n1-hydroperoxycyclohexyl 1-hydroxycyclohexyl peroxide; [1]\n1,1'-dioxybiscyclohexan-1-ol; [2]\ncyclohexylidene hydroperoxide; [3]\ncyclohexanone, peroxide [4]\nC\n201-091-1 [1]\n219-306-2 [2]\n220-279-4 [3]\n235-527-7 [4]\n78-18-2 [1]\n2407-94-5 [2]\n2699-11-8 [3]\n12262-58-7 [4]\nE; R3\nO; R7\nC; R34\nXn; R22\nE; C\nR: 3-7-22-34\nS: (1/2-)3/7-14-36/37/39-45\nC ≥ 25 %: C; R22-34\n10 % ≤ C < 25 %: C; R34\n5 % ≤ C < 10 %: Xi; R36/37/38\n648-002-00-6\nTar oils, brown-coal;\nLight Oil;\n[The distillate from lignite tar boiling in the range of approximately 80 °C to 250 °C (176 °F to 482 °F). Composed primarily of aliphatic and aromatic hydrocarbons and monobasic phenols.]\nH J\n302-674-4\n94114-40-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-003-00-1\nBenzol forerunnings (coal);\nLight Oil Redistillate, low boiling;\n[The distillate from coke oven light oil having an approximate distillation range below 100 °C (212 °F). Composed primarily of C4 to C6 aliphatic hydrocarbons.]\nH J\n266-023-5\n65996-88-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-004-00-7\nDistillates (coal tar), benzole fraction, BTX-rich;\nLight Oil Redistillate, low boiling;\n[A residue from the distillation of crude benzole to remove benzole fronts. Composed primarily of benzene, toluene and xylenes boiling in the range of approximately 75 °C to 200 °C (167 °F to 392 °F).]\nH J\n309-984-9\n101896-26-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-005-00-2\nAromatic hydrocarbons, C6-10, C8-rich;\nLight Oil Redistillate, low boiling\nH J\n292-697-5\n90989-41-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-006-00-8\nSolvent naphtha (coal), light;\nLight Oil Redistillate, low boiling\nH J\n287-498-5\n85536-17-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-007-00-3\nSolvent naphtha (coal), xylene-styrene cut;\nLight Oil Redistillate, intermediate boiling\nH J\n287-502-5\n85536-20-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-008-00-9\nSolvent naphtha (coal), coumarone-styrene contg.;\nLight Oil Redistillate, intermediate boiling\nH J\n287-500-4\n85536-19-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-009-00-4\nNaphtha (coal), distn. residues;\nLight Oil Redistillate, high boiling;\n[The residue remaining from the distillation of recovered naphtha. Composed primarily of naphthalene and condensation products of indene and styrene.]\nH J\n292-636-2\n90641-12-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-010-00-X\nAromatic hydrocarbons, C8;\nLight Oil Redistillate, high boiling\nH J\n292-694-9\n90989-38-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-012-00-0\nAromatic hydrocarbons, C8-9, hydrocarbon resin polymn. by-product;\nLight Oil Redistillate, high boiling;\n[A complex combination of hydrocarbons obtained from the evaporation of solvent under vacuum from polymerized hydrocarbon resin. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C9 and boiling in the range of approximately 120 °C to 215 °C (248 °F to 419 °F).]\nH J\n295-281-1\n91995-20-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-013-00-6\nAromatic hydrocarbons, C9-12, benzene distn.;\nLight Oil Redistillate, high boiling\nH J\n295-551-9\n92062-36-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-014-00-1\nExtract residues (coal), benzole fraction alk., acid ext.;\nLight Oil Extract Residues, low boiling;\n[The redistillate from the distillate, freed of tar acids and tar bases, from bituminous coal high temperature tar boiling in the approximate range of 90 °C to 160 °C (194 °F to 320 °F). It consists predominantly of benzene, toluene and xylenes.]\nH J\n295-323-9\n91995-61-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-015-00-7\nExtract residues (coal tar), benzole fraction alk., acid ext.;\nLight Oil Extract Residues, low boiling;\n[A complex combination of hydrocarbons obtained by the redistillation of the distillate of high temperature coal tar (tar acid and tar base free). It consists predominantly of unsubstituted and substituted mononuclear aromatic hydrocarbons boiling in the range of 85 °C to 195 °C (185 °F to 383 °F).]\nH J\n309-868-8\n101316-63-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-016-00-2\nExtract residues (coal), benzole fraction acid;\nLight Oil Extract Residues, low boiling;\n[An acid sludge by-product of the sulfuric acid refining of crude high temperature coal. Composed primarily of sulfuric acid and organic compounds.]\nH J\n298-725-2\n93821-38-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-017-00-8\nExtract residues (coal), light oil alk., distn. overheads;\nLight Oil Extract Residues, low boiling;\n[The first fraction from the distillation of aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oil boiling substantially below 145 °C (293 °F).Composed primarily of C7 and C8 aliphatic and aromatic hydrocarbons.]\nH J\n292-625-2\n90641-02-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-018-00-3\nExtract residues (coal), light oil alk., acid ext., indene fraction;\nLight Oil Extract Residues, intermediate boiling\nH J\n309-867-2\n101316-62-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-019-00-9\nExtract residues (coal), light oil alk., indene naphtha fraction;\nLight Oil Extract Residues, high boiling;\n[The distillate from aromatic hydrocarbons, coumarone, naphthalene and indene rich prefractionator bottoms or washed carbolic oils, having an approximate boiling range of 155 °C to 180 °C (311 °F to 356 °F).Composed primarily of indene, indan and trimethylbenzenes.]\nH J\n292-626-8\n90641-03-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-020-00-4\nSolvent naphtha (coal);\n[The distillate from either high temperature coal tar, coke oven light oil, or coal tar oil alkaline extract residue having an approximate distillation range of 130 °C to 210 °C (266 °F to 410 °F). Composed primarily of indene and other polycyclic ring systems containing a single aromatic ring. May contain phenolic compounds and aromatic nitrogen bases.]; Light Oil Extract Residues, high boiling\nH J\n266-013-0\n65996-79-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-021-00-X\nDistillates (coal tar), light oils, neutral fraction; Light Oil Extract Residues, high boiling;\n[A distillate from the fractional distillation of high temperature coal tar. Composed primarily of alkyl-substituted one ring aromatic hydrocarbons boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F). May also include unsaturated hydrocarbons such as indene and coumarone.]\nH J\n309-971-8\n101794-90-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-022-00-5\nDistillates (coal tar), light oils, acid exts.; Light Oil Extract Residues, high boiling;\n[This oil is a complex mixture of aromatic hydrocarbons, primarily indene, naphthalene, coumarone, phenol, and o-, m- and p-cresol and boiling in the range of 140 °C to 215 °C (284 °F to 419 °F).]\nH J\n292-609-5\n90640-87-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-023-00-0\nDistillates (coal tar), light oils; Carbolic Oil;\n[A complex combination of hydrocarbons obtained by distillation of coal tar. It consists of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills at the approximate range of 150 °C to 210 °C (302 °F to 410 °F).]\nH J\n283-483-2\n84650-03-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-024-00-6\nTar oils, coal;\nCarbolic Oil;\n[The distillate from high temperature coal tar having an approximate distillation range of 130 °C to 250 °C (266 °F to 410 °F). Composed primarily of naphthalene, alkylnaphthalenes, phenolic compounds, and aromatic nitrogen bases.]\nH J\n266-016-7\n65996-82-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-026-00-7\nExtract residues (coal), light oil alk., acid ext.;\nCarbolic Oil Extract Residue;\n[The oil resulting from the acid washing of alkali-washed carbolic oil to remove the minor amounts of basic compounds (tar bases). Composed primarily of indene, indan and alkylbenzenes.]\nH J\n292-624-7\n90641-01-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-027-00-2\nExtract residues (coal), tar oil alk.;\nCarbolic Oil Extract Residue;\n[The residue obtained from coal tar oil by an alkaline wash such as aqueous sodium hydroxide after the removal of crude coal tar acids. Composed primarily of naphthalenes and aromatic nitrogen bases.]\nH J\n266-021-4\n65996-87-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-028-00-8\nExtract oils (coal), light oil;\nAcid Extract;\n[The aqueous extract produced by an acidic wash of alkali-washed carbolic oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.]\nH J\n292-622-6\n90640-99-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-029-00-3\nPyridine, alkyl derivs.;\nCrude Tar Bases;\n[The complex combination of polyalkylated pyridines derived from coal tar distillation or as high-boiling distillates approximately above 150 °C (302 °F) from the reaction of ammonia with acetaldehyde, formaldehyde or paraformaldehyde.]\nH J\n269-929-9\n68391-11-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-030-00-9\nTar bases, coal, picoline fraction;\nDistillate Bases;\n[Pyridine bases boiling in the range of approximately 125 °C to 160 °C (257 °F 320 °F) obtained by distillation of neutralized acid extract of the base-containing tar fraction obtained by the distillation of bituminous coal tars. Composed chiefly of lutidines and picolines.]\nH J\n295-548-2\n92062-33-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-031-00-4\nTar bases, coal, lutidine fraction;\nDistillate Bases\nH J\n293-766-2\n91082-52-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-032-00-X\nExtract oils (coal), tar base, collidine fraction;\nDistillate Bases;\n[The extract produced by the acidic extraction of bases from crude coal tar aromatic oils, neutralization, and distillation of the bases. Composed primarily of collidines, aniline, toluidines, lutidines, xylidines.]\nH J\n273-077-3\n68937-63-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-033-00-5\nTar bases, coal, collidine fraction;\nDistillate Bases;\n[The distillation fraction boiling in the range of approximately 181 °C to 186 °C (356 °F to 367 °F) from the crude bases obtained from the neutralized, acid-extracted base-containing tar fractions obtained by the distillation of bituminous coal tar. It contains chiefly aniline and collidines.]\nH J\n295-543-5\n92062-28-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-034-00-0\nTar bases, coal, aniline fraction;\nDistillate Bases;\n[The distillation fraction boiling in the range of approximately 180 °C to 200 °C (356 °F to 392 °F) from the crude bases obtained by dephenolating and debasing the carbolated oil from the distillation of coal tar. It contains chiefly aniline, collidines, lutidines and toluidines.]\nH J\n295-541-4\n92062-27-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-035-00-6\nTar bases, coal, toluidine fraction;\nDistillate Bases\nH J\n293-767-8\n91082-53-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-036-00-1\nDistillates (petroleum), alkene-alkyne manuf. pyrolysis oil, mixed with high-temp. coal tar, indene fraction;\nRedistillates;\n[A complex combination of hydrocarbons obtained as a redistillate from the fractional distillation of bituminous coal high temperature tar and residual oils that are obtained by the pyrolytic production of alkenes and alkynes from petroleum products or natural gas. It consists predominantly of indene and boils in a range of approximately 160 °C to 190 °C (320 °F to 374 °F).]\nH J\n295-292-1\n91995-31-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-037-00-7\nDistillates (coal), coal tar-residual pyrolysis oils, naphthalene oils;\nRedistillates;\n[The redistillate obtained from the fractional distillation of bituminous coal high temperature tar and pyrolysis residual oils and boiling in the range of approximately 190 °C to 270 °C (374 °F to 518 °F). Composed primarily of substituted dinuclear aromatics.]\nH J\n295-295-8\n91995-35-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-038-00-2\nExtract oils (coal), coal tar-residual pyrolysis oils, naphthalene oil, redistillate;\nRedistillates;\n[The redistillate from the fractional distillation of dephenolated and debased methylnaphthalene oil obtained from bituminous coal high temperature tar and pyrolysis residual oils boiling in the approximate range of 220 °C to 230 °C (428 °F to 446 °F). It consists predominantly of unsubstituted and substituted dinuclear aromatic hydrocarbons.]\nH J\n295-329-1\n91995-66-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-039-00-8\nExtract oils (coal), coal tar-residual pyrolysis oils, naphthalene oils;\nRedistillates;\n[A neutral oil obtained by debasing and dephenolating the oil obtained from the distillation of high temperature tar and pyrolysis residual oils which has a boiliing range of 225 °C to 255 °C (437 °F to 491 °F). Composed primarily of substituted dinuclear aromatic hydrocarbons.]\nH J\n310-170-0\n122070-79-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-040-00-3\nExtract oils (coal), coal tar residual pyrolysis oils, naphthalene oil, distn. residues;\nRedistillates;\n[Residue from the distillation of dephenolated and debased methylnaphthalene oil (from bituminous coal tar and pyrolysis residual oils) with a boiling range of 240 °C to 260 °C (464 °F to 500 °F). Composed primarily of substituted dinuclear aromatic and heterocyclic hydrocarbons.]\nH J\n310-171-6\n122070-80-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-043-00-X\nCreosote oil, acenaphthene fraction, acenaphthene-free;\nWash Oil Redistillate;\n[The oil remaining after removal by a crystallization process of acenaphthene from acenaphthene oil from coal tar. Composed primarily of naphthalene and alkylnaphthalenes.]\nH M\n292-606-9\n90640-85-0\nCarc. Cat. 2; R45\nT\nR: 45\nS: 53-45\n648-080-00-1\nResidues (coal tar), creosote oil distn.;\nWash Oil Redistillate;\n[The residue from the fractional distillation of wash oil boiling in the approximate range of 270 °C to 330 °C (518 °F to 626 °F). It consists predominantly of dinuclear aromatic and heterocyclic hydrocarbons.]\nH M\n295-506-3\n92061-93-3\nCarc. Cat. 2; R45\nT\nR: 45\nS: 53-45\n648-084-00-3\nDistillates (coal), coke-oven light oil, naphthalene cut;\nNaphthalene Oil;\n[The complex combination of hydrocarbons obtained from prefractionation (continuous distillation) of coke oven light oil. It consists predominantly of naphthalene, coumarone and indene and boils above 148 °C (298 °F).]\nHJM\n285-076-5\n85029-51-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-085-00-9\nDistillates (coal tar), naphthalene oils;\nNaphthalene Oil;\n[A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic and other hydrocarbons, phenolic compounds and aromatic nitrogen compounds and distills in the approximate range of 200 °C to 250 °C (392 °F to 482 °F).]\nHJM\n283-484-8\n84650-04-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-086-00-4\nDistillates (coal tar), naphthalene oils, naphthalene-low;\nNaphthalene Oil Redistillate;\n[A complex combination of hydrocarbons obtained by crystallization of naphthalene oil.Composed primarily of naphthalene, alkyl naphthalenes and phenolic compounds.]\nHJM\n284-898-1\n84989-09-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-087-00-X\nDistillates (coal tar), naphthalene oil crystn. mother liquor;\nNaphthalene Oil Redistillate;\n[A complex combination of organic compounds obtained as a filtrate from the crystallization of the naphthalene fraction from coal tar and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Contains chiefly naphthalene, thionaphthene and alkylnaphthalenes.]\nHJM\n295-310-8\n91995-49-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-088-00-5\nExtract residues (coal), naphthalene oil, alk.;\nNaphthalene Oil Extract Residue;\n[A complex combination of hydrocarbons obtained from the alkali washing of naphthalene oil to remove phenolic compounds (tar acids). It is composed of naphthalene and alkyl naphthalenes.]\nHJM\n310-166-9\n121620-47-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-089-00-0\nExtract residues (coal), naphthalene oil, alk., naphthalene-low;\nNaphthalene Oil Extract Residue;\n[A complex combination of hydrocarbons remaining after the removal of naphthalene from alkali-washed naphthalene oil by a crystallization process. It is composed primarily of naphthalene and alkyl naphthalenes.]\nHJM\n310-167-4\n121620-48-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-090-00-6\nDistillates (coal tar), naphthalene oils, naphthalene-free, alk. exts.;\nNaphthalene Oil Extract Residue;\n[The oil remaining after the removal of phenolic compounds (tar acids) from drained naphthalene oil by an alkali wash. Composed primarily of naphthalene and alkyl naphthalenes.]\nHJM\n292-612-1\n90640-90-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-091-00-1\nExtract residues (coal), naphthalene oil alk., distn. overheads;\nNaphthalene Oil Extract Residue;\n[The distillate from alkali-washed naphthalene oil having an approximate distillation range of 180 °C to 220 °C (356 °F to 428 °F). Composed primarily of naphthalene, alkylbenzenes, indene and indan.]\nHJM\n292-627-3\n90641-04-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-092-00-7\nDistillates (coal tar), naphthalene oils, methylnaphthalene fraction;\nMethylnaphthalene Oil;\n[A distillate from the fractional distillation of high temperature coal tar. Composed primarily of substituted two ring aromatic hydrocarbons and aromatic nitrogen bases boiling in the range of approximately 225 °C to 255 °C (437 °F to 491 °F).]\nHJM\n309-985-4\n101896-27-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-093-00-2\nDistillates (coal tar), naphthalene oils, indole-methylnaphthalene fraction;\nMethylnaphthalene Oil;\n[A distillate from the fractional distillation of high temperature coal tar. Composed primarily of indole and methylnaphthalene boiling in the range of approximately 235 °C to 255 °C (455 °F to 491 °F).]\nHJM\n309-972-3\n101794-91-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-094-00-8\nDistillates (coal tar), naphthalene oils, acid exts.;\nMethylnaphthalene Oil Extract Residue;\n[A complex combination of hydrocarbons obtained by debasing the methylnaphthalene fraction obtained by the distillation of coal tar and boiling in the range of approximately 230 °C to 255 °C (446 °F to 491 °F). Contains chiefly 1(2)-methylnaphthalene, naphthalene, dimethylnaphthalene and biphenyl.]\nHJM\n295-309-2\n91995-48-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-095-00-3\nExtract residues (coal), naphthalene oil alk., distn. residues;\nMethylnaphthalene Oil Extract Residue;\n[The residue from the distillation of alkali-washed naphthalene oil having an approximate distillation range of 220 °C to 300 °C (428 °F to 572 °F). Composed primarily of naphthalene, alkylnaphthalenes and aromatic nitrogen bases.]\nHJM\n292-628-9\n90641-05-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-096-00-9\nExtract oils (coal), acidic, tar-base free;\nMethylnaphthalene Oil Extract Residue;\n[The extract oil boiling in the range of approximately 220 °C to 265 °C (428 °F to 509 °F) from coal tar alkaline extract residue produced by an acidic wash such as aqueous sulfuric acid after distillation to remove tar bases. Composed primarily of alkylnaphthalenes.]\nHJM\n284-901-6\n84989-12-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-097-00-4\nDistillates (coal tar), benzole fraction, distn. residues;\nWash Oil;\n[A complex combination of hydrocarbons obtained from the distillation of crude benzole (high temperature coal tar). It may be a liquid with the approximate distillation range of 150 °C to 300 °C (302 °F to 572 °F) or a semi-solid or solid with a melting point up to 70 °C (158 °F). It is composed primarily of naphthalene and alkyl naphthalenes.]\nHJM\n310-165-3\n121620-46-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-098-00-X\nCreosote oil, acenaphthene fraction;\nWash Oil;\n[A complex combination of hydrocarbons produced by the distillation of coal tar and boiling in the range of approximately 240 °C to 280 °C (464 °F to 536 °F). Composed primarily of acenaphthene, naphthalene and alkyl naphthalene.]\nH M\n292-605-3\n90640-84-9\nCarc. Cat. 2; R45\nT\nR: 45\nS: 53-45\n648-099-00-5\nCreosote oil;\n[A complex combination of hydrocarbons obtained by the distillation of coal tar. It consists primarily of aromatic hydrocarbons and may contain appreciable quantities of tar acids and tar bases. It distills at the approximate range of 200 °C to 325 °C (392 °F to 617 °F).]\nH M\n263-047-8\n61789-28-4\nCarc. Cat. 2; R45\nT\nR: 45\nS: 53-45\n648-100-00-9\nCreosote oil, high-boiling distillate;\nWash Oil;\n[The high-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillates, removed. It is crystal free at approximately 5 °C (41 °F).]\nH M\n274-565-9\n70321-79-8\nCarc. Cat. 2; R45\nT\nR: 45\nS: 53-45\n648-102-00-X\nExtract residues (coal), creosote oil acid;\nWash Oil Extract Residue;\n[A complex combination of hydrocarbons from the base-freed fraction from the distillation of coal tar, boiling in the range of approximately 250 °C to 280 °C (482 °F to 536 °F). It consists predominantly of biphenyl and isomeric diphenylnaphthalenes.]\nH M\n310-189-4\n122384-77-4\nCarc. Cat. 2; R45\nT\nR: 45\nS: 53-45\n648-103-00-5\nAnthracene oil, anthracene paste;\nAnthracene Oil Fraction;\n[The anthracene-rich solid obtained by the crystallization and centrifuging of anthracene oil. It is composed primarily of anthracene, carbazole and phenanthrene.]\nHJM\n292-603-2\n90640-81-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-104-00-0\nAnthracene oil, anthracene-low;\nAnthracene Oil Fraction;\n[The oil remaining after the removal, by a crystallization process, of an anthracene-rich solid (anthracene paste) from anthracene oil. It is composed primarily of two, three and four membered aromatic compounds.]\nHJM\n292-604-8\n90640-82-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-105-00-6\nResidues (coal tar), anthracene oil distn.;\nAnthracene Oil Fraction;\n[The residue from the fraction distillation of crude anthracene boiling in the approximate range of 340 °C to 400 °C (644 °F to 752 °F). It consists predominantly of tri- and polynuclear aromatic and heterocyclic hydrocarbons.]\nHJM\n295-505-8\n92061-92-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-106-00-1\nAnthracene oil, anthracene paste, anthracene fraction;\nAnthracene Oil Fraction;\n[A complex combination of hydrocarbons from the distillation of anthracene obtained by the crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of 330 °C to 350 °C (626 °F to 662 °F). It contains chiefly anthracene, carbazole and phenanthrene.]\nHJM\n295-275-9\n91995-15-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-107-00-7\nAnthracene oil, anthracene paste, carbazole fraction;\nAnthracene Oil Fraction;\n[A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous coal high temperature tar and boiling in the approximate range of 350 °C to 360 °C (662 °F to 680 °F). It contains chiefly anthracene, carbazole and phenanthrene.]\nHJM\n295-276-4\n91995-16-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-108-00-2\nAnthracene oil, anthracene paste, distn. lights;\nAnthracene Oil Fraction;\n[A complex combination of hydrocarbons from the distillation of anthracene obtained by crystallization of anthracene oil from bituminous high temperature tar and boiling in the range of approximately 290 °C to 340 °C (554 °F to 644 °F). It contains chiefly trinuclear aromatics and their dihydro derivatives.]\nHJM\n295-278-5\n91995-17-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-109-00-8\nTar oils, coal, low-temp.;\nTar Oil, high boiling;\n[A distillate from low-temperature coal tar. Composed primarily of hydrocarbons, phenolic compounds and aromatic nitrogen bases boiling in the range of approximately 160 °C to 340 °C (320 °F to 644 °F).]\nHJM\n309-889-2\n101316-87-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-110-00-3\nExtract residues (coal), low temp. coal atar alk.;\n[The residue from low temperature coal tar oils after an alkaline wash, such as aqueous sodium hydroxide, to remove crude coal tar acids. Composed primarily of hydrocarbons and aromatic nitrogen bases.]\nHJM\n310-191-5\n122384-78-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-111-00-9\nPhenols, ammonia liquor ext.;\nAlkaline Extract;\n[The combination of phenols extracted, using isobutyl acetate, from the ammonia liquor condensed from the gas evolved in low-temperature (less than 700 °C (1 292 °F)) destructive distillation of coal. It consists predominantly of a mixture of monohydric and dihydric phenols.]\nHJM\n284-881-9\n84988-93-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-112-00-4\nDistillates (coal tar), light oils, alk. exts.;\nAlkaline Extract;\n[The aqueous extract from carbolic oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.]\nHJM\n292-610-0\n90640-88-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-113-00-X\nExtracts, coal tar oil alk.;\nAlkaline Extract;\n[The extract from coal tar oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.]\nHJM\n266-017-2\n65996-83-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-114-00-5\nDistillates (coal tar), naphthalene oils, alk. exts.;\nAlkaline Extract;\n[The aqueous extract from naphthalene oil produced by an alkaline wash such as aqueous sodium hydroxide. Composed primarily of the alkali salts of various phenolic compounds.]\nHJM\n292-611-6\n90640-89-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-115-00-0\nExtract residues (coal), tar oil alk., carbonated, limed;\nCrude Phenols;\n[The product obtained by treatment of coal tar oil alkaline extract with CO2 and CaO. Composed primarily of CaCO3, Ca(OH)2, Na2CO3 and other organic and inorganic impurities.]\nHJM\n292-629-4\n90641-06-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-116-00-6\nTar acids, coal, crude;\nCrude Phenols;\n[The reaction product obtained by neutralizing coal tar oil alkaline extract with an acidic solution, such as aqueous sulfuric acid, or gaseous carbon dioxide, to obtain the free acids. Composed primarily of tar acids such as phenol, cresols, and xylenols.]\nHJM\n266-019-3\n65996-85-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-117-00-1\nTar acids, brown-coal, crude;\nCrude Phenols;\n[An acidified alkaline extract of brown coal tar distillate. Composed primarily of phenol and phenol homologs.]\nHJM\n309-888-7\n101316-86-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-118-00-7\nTar acids, brown-coal gasification;\nCrude Phenols;\n[A complex combination of organic compounds obtained from brown coal gasification. Composed primarily of C6-10 hydroxy aromatic phenols and their homologs.]\nHJM\n295-536-7\n92062-22-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-119-00-2\nTar acids, distn. residues;\nDistillate Phenols;\n[A residue from the distillation of crude phenol from coal. It consists predominantly of phenols having carbon numbers in the range of C8 through C10 with a softening point of 60 °C to 80 °C (140 °F to 176 °F).]\nHJM\n306-251-5\n96690-55-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-120-00-8\nTar acids, methylphenol fraction;\nDistillate Phenols;\n[The fraction of tar acid rich in 3- and 4-methylphenol, recovered by distillation of low-temperature coal tar crude tar acids.]\nHJM\n284-892-9\n84989-04-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-121-00-3\nTar acids, polyalkylphenol fraction;\nDistillate Phenols;\n[The fraction of tar acids, recovered by distillation of low-temperature coal tar crude tar acids, having an approximate boiling range of 225 °C to 320 °C (437 °F to 608 °F).Composed primarily of polyalkylphenols.]\nHJM\n284-893-4\n84989-05-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-122-00-9\nTar acids, xylenol fraction;\nDistillate Phenols;\n[The fraction of tar acids, rich in 2,4- and 2,5-dimethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.]\nHJM\n284-895-5\n84989-06-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-123-00-4\nTar acids, ethylphenol fraction;\nDistillate Phenols;\n[The fraction of tar acids, rich in 3- and 4-ethylphenol, recovered by distillation of low-temperature coal tar crude tar acids.]\nHJM\n284-891-3\n84989-03-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-124-00-X\nTar acids, 3,5-xylenol fraction;\nDistillate Phenols;\n[The fraction of tar acids, rich in 3,5-dimethylphenol, recovered by distillation of low-temperature coal tar acids.]\nHJM\n284-896-0\n84989-07-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-125-00-5\nTar acids, residues, distillates, first-cut;\nDistillate Phenols;\n[The residue from the distillation in the range of 235 °C to 355 °C (481 °F to 697 °F) of light carbolic oil.]\nHJM\n270-713-1\n68477-23-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-126-00-0\nTar acids, cresylic, residues;\nDistillate Phenols;\n[The residue from crude coal tar acids after removal of phenol, cresols, xylenols and any higher boiling phenols. A black solid with a melting point approximately 80 °C (176 °F). Composed primarily of polyalkylphenols, resin gums, and inorganic salts.]\nHJM\n271-418-0\n68555-24-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-127-00-6\nPhenols, C9-11;\nDistillate Phenols\nHJM\n293-435-2\n91079-47-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-128-00-1\nTar acids, cresylic;\nDistillate Phenols;\n[A complex combination of organic compounds obtained from brown coal and boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). It contains chiefly phenols and pyridine bases.]\nHJM\n295-540-9\n92062-26-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-129-00-7\nTar acids, brown-coal, C2-alkylphenol fraction;\nDistillate Phenols;\n[The distillate from the acidification of alkaline washed lignite tar distillate boiling in the range of approximately 200 °C to 230 °C (392 °F to 446 °F). Composed primarily of m- and p-ethylphenol as well as cresols and xylenols.]\nHJM\n302-662-9\n94114-29-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-130-00-2\nExtract oils (coal), naphthalene oils;\nAcid Extract;\n[The aqueous extract produced by an acidic wash of alkali-washed naphthalene oil. Composed primarily of acid salts of various aromatic nitrogen bases including pyridine, quinoline and their alkyl derivatives.]\nHJM\n292-623-1\n90641-00-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-131-00-8\nTar bases, quinoline derivs.;\nDistillate Bases\nHJM\n271-020-7\n68513-87-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-132-00-3\nTar bases, coal, quinoline derivs. fraction;\nDistillate Bases\nHJM\n274-560-1\n70321-67-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-133-00-9\nTar bases, coal, distn. residues;\nDistillate Bases;\n[The distillation residue remaining after the distillation of the neutralized, acid-extracted base-containing tar fractions obtained by the distillation of coal tars. It contains chiefly aniline, collidines, quinoline and quinoline derivatives and toluidines.]\nHJM\n295-544-0\n92062-29-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-134-00-4\nHydrocarbon oils, arom., mixed with polyethylene and polypropylene, pyrolyzed, light oil fraction;\nHeat Treatment Products;\n[The oil obtained from the heat treatment of a polyethylene/polypropylene mixture with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 120 °C (158 °F to 248 °F).]\nHJM\n309-745-9\n100801-63-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-135-00-X\nHydrocarbon oils, arom., mixed with polyethylene, pyrolyzed, light oil fraction;\nHeat Treatment Products;\n[The oil obtained from the heat treatment of polyethylene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of 70 °C to 120 °C (158 °F to 248 °F).]\nHJM\n309-748-5\n100801-65-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-136-00-5\nHydrocarbon oils, arom., mixed with polystyrene, pyrolyzed, light oil fraction;\nHeat Treatment Products;\n[The oil obtained from the heat treatment of polystyrene with coal tar pitch or aromatic oils. It consists predominantly of benzene and its homologs boiling in a range of approximately 70 °C to 210 °C (158 °F to 410 °F).]\nHJM\n309-749-0\n100801-66-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-137-00-0\nExtract residues (coal), tar oil alk., naphthalene distn. residues;\nNaphthalene Oil Extract Residue;\n[The residue obtained from chemical oil extracted after the removal of naphthalene by distillation composed primarily of two to four membered condensed ring aromatic hydrocarbons and aromatic nitrogen bases.]\nHJM\n277-567-8\n73665-18-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-138-00-6\nCreosote oil, low-boiling distillate;\nWash Oil;\n[The low-boiling distillation fraction obtained from the high temperature carbonization of bituminous coal, which is further refined to remove excess crystalline salts. It consists primarily of creosote oil with some of the normal polynuclear aromatic salts, which are components of coal tar distillate, removed. It is crystal free at approximately 38 °C (100 °F).]\nH M\n274-566-4\n70321-80-1\nCarc. Cat. 2; R45\nT\nR: 45\nS: 53-45\n648-139-00-1\nTar acids, cresylic, sodium salts, caustic solns.;\nAlkaline Extract\nHJM\n272-361-4\n68815-21-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-140-00-7\nExtract oils (coal), tar base;\nAcid Extract;\n[The extract from coal tar oil alkaline extract residue produced by an acidic wash such as aqueous sulfuric acid after distillation to remove naphthalene. Composed primarily of the acid salts of various aromatic nitrogen bases including pyridine, quinoline, and their alkyl derivatives.]\nHJM\n266-020-9\n65996-86-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-141-00-2\nTar bases, coal, crude;\nCrude Tar Bases;\n[The reaction product obtained by neutralizing coal tar base extract oil with an alkaline solution, such as aqueous sodium hydroxide, to obtain the free bases. Composed primarily of such organic bases as acridine, phenanthridine, pyridine, quinoline and their alkyl derivatives.]\nHJM\n266-018-8\n65996-84-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-147-00-5\nLight oil (coal), coke-oven;\nCrude benzole;\n[The volatile organic liquid extracted from the gas evolved in the high temperature (greater than 700 °C (1 292 °F)) destructive distillation of coal. Composed primarily of benzene, toluene, and xylenes. May contain other minor hydrocarbon constituents.]\nH J\n266-012-5\n65996-78-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-148-00-0\nDistillates (coal), liq. solvent extn., primary;\n[The liquid product of condensation of vapors emitted during the digestion of coal in a liquid solvent and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of partly hydrogenated condensed-ring aromatic hydrocarbons, aromatic compounds containing nitrogen, oxygen and sulfur, and their alkyl derivatives having carbon numbers predominantly in the range of C4 through C14.]\nH J\n302-688-0\n94114-52-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-149-00-6\nDistillates (coal), solvent extn., hydrocracked;\n[Distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 300 °C (86 °F to 572 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 through C14. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.]\nH J\n302-689-6\n94114-53-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-150-00-1\nNaphtha (coal), solvent extn., hydrocracked;\n[Fraction of the distillate obtained by hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 30 °C to 180 °C (86 °F to 356 °F). Composed primarily of aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes with carbon numbers predominantly in the range of C4 to C9. Nitrogen, sulfur and oxygen-containing aromatic and hydrogenated aromatic compounds are also present.]\nH J\n302-690-1\n94114-54-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-152-00-2\nDistillates (coal), solvent extn., hydrocracked middle;\n[Distillate obtained from the hydrocracking of coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 300 °C (356 °F to 572 °F. Composed primarily of two-ring aromatic, hydrogenated aromatic and naphthenic compounds, their alkyl derivatives and alkanes having carbon numbers predominantly in the range of C9 through C14. Nitrogen, sulfur and oxygen-containing compounds are also present.]\nH J\n302-692-2\n94114-56-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-153-00-8\nDistillates (coal), solvent extn., hydrocracked hydrogenated middle;\n[Distillate from the hydrogenation of hydrocracked middle distillate from coal extract or solution produced by the liquid solvent extraction or supercritical gas extraction processes and boiling in the range of approximately 180 °C to 280 °C (356 °F to 536 °F). Composed primarily of hydrogenated two- ring carbon compounds and their alkyl derivatives having carbon numbers predominantly in the range of C9 through C14.]\nH J\n302-693-8\n94114-57-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n648-156-00-4\nLight oil (coal), semi-coking process;\nFresh oil;\n[The volatile organic liquid condensed from the gas evolved in the low-temperature (less than 700 °C (1 292 °F)) destructive distillation of coal. Composed primarily of C6-10 hydrocarbons.]\nH J\n292-635-7\n90641-11-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nT\nR: 45-46\nS: 53-45\n649-062-00-6\nGases (petroleum), catalytic cracked naphtha depropanizer overhead, C3-rich acid-free;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from fractionation of catalytic cracked hydrocarbons and treated to remove acidic impurities. It consists of hydrocarbons having carbon numbers in the range of C2 through C4, predominantly C3.]\nH K\n270-755-0\n68477-73-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-063-00-1\nGases (petroleum), catalytic cracker;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of the products from a catalytic cracking process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n270-756-6\n68477-74-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-064-00-7\nGases (petroleum), catalytic cracker, C1-5-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of aliphatic hydrocarbons having carbon numbers in the range of C1 through C6, predominantly C1 through C5.]\nH K\n270-757-1\n68477-75-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-065-00-2\nGases (petroleum), catalytic polymd. naphtha stabilizer overhead, C2-4-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the fractionation stabilization of catalytic polymerized naphtha. It consists of aliphatic hydrocarbons having carbon numbers in the range of C2 through C6, predominantly C2 through C4.]\nH K\n270-758-7\n68477-76-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-066-00-8\nGases (petroleum), catalytic reformer, C1-4-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers in the range of C1 through C6, predominantly C1 through C4.]\nH K\n270-760-8\n68477-79-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-067-00-3\nGases (petroleum), C3-5 olefinic-paraffinic alkylation feed;\nPetroleum gas;\n[A complex combination of olefinic and paraffinic hydrocarbons having carbon numbers in the range of C3 through C5 which are used as alkylation feed. Ambient temperatures normally exceed the critical temperature of these combinations.]\nH K\n270-765-5\n68477-83-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-068-00-9\nGases (petroleum), C4-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by distillation of products from a catalytic fractionation process. It consists of aliphatic hydrocarbons having carbon numbers in the range of C3 through C5, predominantly C4.]\nH K\n270-767-6\n68477-85-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-069-00-4\nGases (petroleum), deethanizer overheads;\nPetroleum gas;\n[A complex combination of hydrocarbons produced from distillation of the gas and gasoline fractions from the catalytic cracking process. It contains predominantly ethane and ethylene.]\nH K\n270-768-1\n68477-86-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-070-00-X\nGases (petroleum), deisobutanizer tower overheads;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the atmospheric distillation of a butane-butylene stream. It consists of aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C4.]\nH K\n270-769-7\n68477-87-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-071-00-5\nGases (petroleum), depropanizer dry, propene-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of products from the gas and gasoline fractions of a catalytic cracking process. It consists predominantly of propylene with some ethane and propane.]\nH K\n270-772-3\n68477-90-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-072-00-0\nGases (petroleum), depropanizer overheads;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by distillation of products from the gas and gasoline fractions of a catalytic cracking process. It consists of aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C4.]\nH K\n270-773-9\n68477-91-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-073-00-6\nGases (petroleum), gas recovery plant depropanizer overheads;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by fractionation of miscellaneous hydrocarbon streams. It consists predominantly of hydrocarbons having carbon numbers in the range of C1 through C4, predominantly propane.]\nH K\n270-777-0\n68477-94-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-074-00-1\nGases (petroleum), Girbotol unit feed;\nPetroleum gas;\n[A complex combination of hydrocarbons that is used as the feed into the Girbatol unit to remove hydrogen sulfide. It consists of aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C4.]\nH K\n270-778-6\n68477-95-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-075-00-7\nGases (petroleum), isomerized naphtha fractionator, C4-rich, hydrogen sulfide-free;\nPetroleum gas\nH K\n270-782-8\n68477-99-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-076-00-2\nTail gas (petroleum), catalytic cracked clarified oil and thermal cracked vacuum residue fractionation reflux drum;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from fractionation of catalytic cracked clarified oil and thermal cracked vacuum residue. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n270-802-5\n68478-21-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-077-00-8\nTail gas (petroleum), catalytic cracked naphtha stabilization absorber;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the stabilization of catalytic cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n270-803-0\n68478-22-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-078-00-3\nTail gas (petroleum), catalytic cracker, catalytic reformer and hydrodesulfurizer combined fractionater;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the fractionation of products from catalytic cracking, catalytic reforming and hydrodesulfurizing processes treated to remove acidic impurities. It consists predominantly of hydrocarbons having cabon numbers predominantly in the range of C1 through C5.]\nH K\n270-804-6\n68478-24-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-079-00-9\nTail gas (petroleum), catalytic reformed naphtha fractionation stabilizer;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the fractionation stabilization of catalytic reformed naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n270-806-7\n68478-26-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-080-00-4\nTail gas (petroleum), saturate gas plant mixed stream, C4-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the fractionation stabilization of straight-run naphtha, distillation tail gas and catalytic reformed naphtha stabilizer tail gas. It consists of hydrocarbons having carbon numbers in the range of C3 through C6, predominantly butane and isobutane.]\nH K\n270-813-5\n68478-32-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-081-00-X\nTail gas (petroleum), saturate gas recovery plant, C1-2-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from fractionation of distillate tail gas, straight-run naphtha, catalytic reformed naphtha stabilizer tail gas. It consists predominantly of hydrocarbons having carbon numbers in the range of C1through C5, predominantly methane and ethane.]\nH K\n270-814-0\n68478-33-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-082-00-5\nTail gas (petroleum), vacuum residues thermal cracker;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the thermal cracking of vacuum residues. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n270-815-6\n68478-34-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-083-00-0\nHydrocarbons, C3-4-rich, petroleum distillate;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by distillation and condensation of crude oil. It consists of hydrocarbons having carbon numbers in the range of C3 through C5, predominantly C3 through C4.]\nH K\n270-990-9\n68512-91-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-084-00-6\nGases (petroleum), full-range straight-run naphtha dehexanizer off;\npetroleum gas;\n[A complex combination of hydrocarbons obtained by the fractionation of the full-range straight-run naphtha. It consists of hydrocarbons having carbon numbers predominantly in the range of C2 through C6.]\nH K\n271-000-8\n68513-15-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-085-00-1\nGases (petroleum), hydrocracking depropanizer off, hydrocarbon-rich;\nPetroleum gas;\n[A complex combination of hydrocarbon produced by the distillation of products from a hydrocracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C4. It may also contain small amounts of hydrogen and hydrogen sulfide.]\nH K\n271-001-3\n68513-16-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-086-00-7\nGases (petroleum), light straight-run naphtha stabilizer off;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by the stabilization of light straight-run naphtha. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C6.]\nH K\n271-002-9\n68513-17-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-087-00-2\nResidues (petroleum), alkylation splitter, C4-rich;\nPetroleum gas;\n[A complex residuum from the distillation of streams various refinery operations. It consists of hydrocarbons having carbon numbers in the range of C4 through C5, predominantly butane and boiling in the range of approximately -11.7 °C to 27.8 °C (11 °F to 82 °F).]\nH K\n271-010-2\n68513-66-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-088-00-8\nHydrocarbons, C1-4;\nPetroleum gas;\n[A complex combination of hydrocarbons provided by thermal cracking and absorber operations and by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately minus 164 °C to minus 0.5 °C (-263 °F to 31 °F).]\nH K\n271-032-2\n68514-31-8\nF+; R12\nCarc. Cat 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-089-00-3\nHydrocarbons, C1-4, sweetened;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by subjecting hydrocarbon gases to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately -164 °C to -0.5 °C (-263 °F to 31 °F).]\nH K\n271-038-5\n68514-36-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-090-00-9\nHydrocarbons, C1-3;\nPetroleum gas;\n[A complex combination of hydrocarbons having carbon numbers predominantly in the range of C1 through C3 and boiling in the range of approximately minus 164 °C to minus 42 °C (-263 °F to -44 °F).]\nH K\n271-259-7\n68527-16-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-091-00-4\nHydrocarbons, C1-4, debutanizer fraction;\nPetroleum gas\nH K\n271-261-8\n68527-19-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-092-00-X\nGases (petroleum), C1-5, wet;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of crude oil and/or the cracking of tower gas oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n271-624-0\n68602-83-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-093-00-5\nHydrocarbons, C2-4;\nPetroleum gas\nH K\n271-734-9\n68606-25-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-094-00-0\nHydrocarbons, C3;\nPetroleum gas\nH K\n271-735-4\n68606-26-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-095-00-6\nGases (petroleum), alkylation feed;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the catalytic cracking of gas oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C4.]\nH K\n271-737-5\n68606-27-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-096-00-1\nGases (petroleum), depropanizer bottoms fractionation off;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the fractionation of depropanizer bottoms. It consists predominantly of butane, isobutane and butadiene.]\nH K\n271-742-2\n68606-34-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-097-00-7\nGases (petroleum), refinery blend;\nPetroleum gas;\n[A complex combination obtained from various processes. It consists of hydrogen, hydrogen sulfide and hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n272-183-7\n68783-07-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-098-00-2\nGases (petroleum), catalytic cracking;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of the products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C3 through C5.]\nH K\n272-203-4\n68783-64-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-099-00-8\nGases (petroleum), C2-4, sweetened;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C2 through C4 and boiling in the range of approximately -51 °C to -34 °C (-60 °F to -30 °F).]\nH K\n272-205-5\n68783-65-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-100-00-1\nGases (petroleum), crude oil fractionation off;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the fractionation of crude oil. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n272-871-7\n68918-99-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-101-00-7\nGases (petroleum), dehexanizer off;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by the fractionation of combined naphtha streams. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n272-872-2\n68919-00-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-102-00-2\nGases (petroleum), light straight run gasoline fractionation stabilizer off;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by the fractionation of light straight-run gasoline. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n272-878-5\n68919-05-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-103-00-8\nGases (petroleum), naphtha unifiner desulfurization stripper off;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by a naphtha unifiner desulfurization process and stripped from the naphtha product. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n272-879-0\n68919-06-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-104-00-3\nGases (petroleum), straight-run naphtha catalytic reforming off;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by the catalytic reforming of straight-run naphtha and fractionation of the total effluent. It consists of methane, ethane, and propane.]\nH K\n272-882-7\n68919-09-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-105-00-9\nGases (petroleum), fluidized catalytic cracker splitter overheads;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the fractionation of the charge to the C3 -C4 splitter. It consists predominantly of C3 hydrocarbons.]\nH K\n272-893-7\n68919-20-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-106-00-4\nGases (petroleum), straight-run stabilizer off;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the fractionation of the liquid from the first tower used in the distillation of crude oil. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n272-883-2\n68919-10-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-107-00-X\nGases (petroleum), catalytic cracked naphtha debutanizer;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from fractionation of catalytic cracked naphtha. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n273-169-3\n68952-76-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-108-00-5\nTail gas (petroleum), catalytic cracked distillate and naphtha stabilizer;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by the fractionation of catalytic cracked naphtha and distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n273-170-9\n68952-77-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-109-00-0\nTail gas (petroleum), thermal-cracked distillate, gas oil and naphtha absorber;\npetroleum gas;\n[A complex combination of hydrocarbons obtained from the separation of thermal-cracked distillates, naphtha and gas oil. It consists pedrominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n273-175-6\n68952-81-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-110-00-6\nTail gas (petroleum), thermal cracked hydrocarbon fractionation stabilizer, petroleum coking;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the fractionation stabilization of thermal cracked hydrocarbons from petroleum coking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n273-176-1\n68952-82-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-111-00-1\nGases (petroleum, light steam-cracked, butadiene conc.;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of products from a thermal cracking process. It consists of hydrocarbons having a carbon number predominantly of C4.]\nH K\n273-265-5\n68955-28-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-112-00-7\nGases (petroleum), straight-run naphtha catalytic reformer stabilizer overhead;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by the catalytic reforming of straight-run naphtha and the fractionation of the total effluent. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C4.]\nH K\n273-270-2\n68955-34-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-113-00-2\nHydrocarbons, C4;\nPetroleum gas\nH K\n289-339-5\n87741-01-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-114-00-8\nAlkanes, C1-4, C3-rich;\nPetroleum gas\nH K\n292-456-4\n90622-55-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-115-00-3\nGases (petroleum), steam-cracker C3-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of products from a steam cracking process. It consists predominantly of propylene with some propane and boils in the range of approximately -70 °C to 0 °C (-94 °F to 32 °F).]\nH K\n295-404-9\n92045-22-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-116-00-9\nHydrocarbons, C4, steam-cracker distillate;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of the products of a steam cracking process. It consists predominantly of hydrocarbons having a carbon number of C4, predominantly 1-butene and 2-butene, containing also butane and isobutene and boiling in the range of approximately minus 12 °C to 5 °C (10.4 °F to 41 °F).]\nH K\n295-405-4\n92045-23-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-117-00-4\nPetroleum gases, liquefied, sweetened, C4 fraction;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by subjecting a liquified petroleum gas mix to a sweetening process to oxidize mercaptans or to remove acidic impurities. It consists predominantly of C4 saturated and unsaturated hydrocarbons.]\nHKS\n295-463-0\n92045-80-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-118-00-X\nHydrocarbons, C4, 1,3-butadiene- and isobutene-free;\nPetroleum gas\nH K\n306-004-1\n95465-89-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-119-00-5\nRaffinates (petroleum), steam-cracked C4 fraction cuprous ammonium acetate extn., C3-5 and C3-5 unsatd., butadiene-free;\nPetroleum gas\nH K\n307-769-4\n97722-19-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-120-00-0\nGases (petroleum), amine system feed;\nRefinery gas;\n[The feed gas to the amine system for removal of hydrogen sulfide. It consists of hydrogen. Carbon monoxide, carbon dioxide, hydrogen sulfide and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5 may also be present.]\nH K\n270-746-1\n68477-65-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-121-00-6\nGases (petroleum), benzene unit hydrodesulfurizer off;\nRefinery gas;\n[Off gases produced by the benzene unit. It consists primarily of hydrogen. Carbon monoxide and hydrocarbons having carbon numbers predominantly in the range of C1 through C6, including benzene, may also be present.]\nH K\n270-747-7\n68477-66-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-122-00-1\nGases (petroleum), benzene unit recycle, hydrogen-rich;\nRefinery gas;\n[A complex combination of hydrocarbons obtained by recycling the gases of the benzene unit. It consists primarily of hydrogen with various small amounts of carbon monoxide and hydrocarbons having carbon numbers in the range of C1 through C6.]\nH K\n270-748-2\n68477-67-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-123-00-7\nGases (petroleum), blend oil, hydrogen-nitrogen-rich;\nRefinery gas;\n[A complex combination of hydrocarbons obtained by distillation of a blend oil. It consists primarily of hydrogen and nitrogen with various small amounts of carbon monoxide, carbon dioxide, and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n270-749-8\n68477-68-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-124-00-2\nGases (petroleum), catalytic reformed naphtha stripper overheads;\nRefinery gas;\n[A complex combination of hydrocarbons obtained from stabilization of catalytic reformed naphtha. Its consists of hydrogen and saturated hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n270-759-2\n68477-77-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-125-00-8\nGases (petroleum), C6-8 catalytic reformer recycle;\nRefinery gas;\n[A complex combination of hydrocarbons produced by distillation of products from catalytic reforming of C6-C8 feed and recycled to conserve hydrogen. It consists primarily of hydrogen. It may also contain various small amounts of carbon monoxide, carbon dioxide, nitrogen, and hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n270-761-3\n68477-80-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-126-00-3\nGases (petroleum), C6-8 catalytic reformer;\nRefinery gas;\n[A complex combination of hydrocarbons produced by distillation of products from catalytic reforming of C6-C8feed. It consists of hydrocarbons having carbon numbers in the range of C1 through C5 and hydrogen.]\nH K\n270-762-9\n68477-81-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-127-00-9\nGases (petroleum), C6-8 catalytic reformer recycle, hydrogen-rich;\nRefinery gas\nH K\n270-763-4\n68477-82-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-128-00-4\nGases (petroleum), C2-return stream;\nRefinery gas;\n[A complex combination of hydrocarbons obtained by the extraction of hydrogen from a gas stream which consists primarily of hydrogen with small amounts of nitrogen, carbon monoxide, methane, ethane, and ethylene. It contains predominantly hydrocarbons such as methane, ethane, and ethylene with small amounts of hydrogen, nitrogen and carbon monoxide.]\nH K\n270-766-0\n68477-84-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-129-00-X\nGases (petroleum), dry sour, gas-concn.-unit-off;\nRefinery gas;\n[The complex combination of dry gases from a gas concentration unit. It consists of hydrogen, hydrogen sulfide and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.]\nH K\n270-774-4\n68477-92-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-130-00-5\nGases (petroleum), gas concn. reabsorber distn.;\nRefinery gas;\n[A complex combination of hydrocarbons produced by distillation of products from combined gas streams in a gas concentration reabsorber. It consists predominantly of hydrogen, carbon monoxide, carbon dioxide, nitrogen, hydrogen sulfide and hydrocarbons having carbon numbers in the range of C1 through C3.]\nH K\n270-776-5\n68477-93-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-131-00-0\nGases (petroleum), hydrogen absorber off;\nRefinery gas;\n[A complex combination obtained by absorbing hydrogen from a hydrogen rich stream. It consists of hydrogen, carbon monoxide, nitrogen, and methane with small amounts of C2 hydrocarbons.]\nH K\n270-779-1\n68477-96-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-132-00-6\nGases (petroleum), hydrogen-rich;\nRefinery gas;\n[A complex combination separated as a gas from hydrocarbon gases by chilling. It consists primarily of hydrogen with various small amounts of carbon monoxide, nitrogen, methane, and C2 hydrocarbons.]\nH K\n270-780-7\n68477-97-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-133-00-1\nGases (petroleum), hydrotreater blend oil recycle, hydrogen-nitrogen-rich;\nRefinery gas;\n[A complex combination obtained from recycled hydrotreated blend oil. It consists primarily of hydrogen and nitrogen with various small amounts of carbon monoxide, carbon dioxide and hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n270-781-2\n68477-98-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-134-00-7\nGases (petroleum), recycle, hydrogen-rich;\nRefinery gas;\n[A complex combination obtained from recycled reactor gases. It consists primarily of hydrogen with various small amounts of carbon monoxide, carbon dioxide, nitrogen, hydrogen sulfide, and saturated aliphatic hydrocarbons having carbon numbers in the range of C1 through C5.]\nH K\n270-783-3\n68478-00-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-135-00-2\nGases (petroleum), reformer make-up, hydrogen-rich;\nRefinery gas;\n[A complex combination obtained from the reformers. It consists primarily of hydrogen with various small amounts of carbon monoxide and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n270-784-9\n68478-01-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-136-00-8\nGases (petroleum), reforming hydrotreater;\nRefinery gas;\n[A complex combination obtained from the reforming hydrotreating process. It consists primarily of hydrogen, methane, and ethane with various small amounts of hydrogen sulfide and aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C5.]\nH K\n270-785-4\n68478-02-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-137-00-3\nGases (petroleum), reforming hydrotreater, hydrogen-methane-rich;\nRefinery gas;\n[A complex combination obtained from the reforming hydrotreating process. It consists primarily of hydrogen and methane with various small amounts of carbon monoxide, carbon dioxide, nitrogen and saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C5.]\nH K\n270-787-5\n68478-03-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-138-00-9\nGases (petroleum), reforming hydrotreater make-up, hydrogen-rich;\nRefinery gas;\n[A complex combination obtained from the reforming hydrotreating process. It consists primarily of hydrogen with various small amounts of carbon monoxide and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n270-788-0\n68478-04-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-139-00-4\nGases (petroleum), thermal cracking distn.;\nRefinery gas;\n[A complex combination produced by distillation of products from a thermal cracking process. It consists of hydrogen, hydrogen sulfide, carbon monoxide, carbon dioxide and hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n270-789-6\n68478-05-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-140-00-X\nTail gas (petroleum), catalytic cracker refractionation absorber;\nRefinery gas;\n[A complex combination of hydrocarbons obtained from refractionation of products from a catalytic cracking process. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.]\nH K\n270-805-1\n68478-25-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-141-00-5\nTail gas (petroleum), catalytic reformed naphtha separator;\nRefinery gas;\n[A complex combination of hydrocarbons obtained from the catalytic reforming of straight run naphtha. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n270-807-2\n68478-27-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-142-00-0\nTail gas (petroleum), catalytic reformed naphtha stabilizer;\nRefinery gas;\n[A complex combination of hydrocarbons obtained from the stabilization of catalytic reformed naphtha. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n270-808-8\n68478-28-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-143-00-6\nTail gas (petroleum), cracked distillate hydrotreater separator;\nRefinery gas;\n[A complex combination of hydrocarbons obtained by treating cracked distillates with hydrogen in the presence of a catalyst. It consists of hydrogen and saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n270-809-3\n68478-29-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-144-00-1\nTail gas (petroleum), hydrodesulfurized straight-run naphtha separator;\nRefinery gas;\n[A complex combination of hydrocarbons obtained from hydrodesulfurization of straight-run naphtha. It consists of hydrogen and saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n270-810-9\n68478-30-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-145-00-7\nGases (petroleum), catalytic reformed straight-run naphtha stabilizer overheads;\nRefinery gas;\n[A complex combination of hydrocarbons obtained from the catalytic reforming of straight-run naphtha followed by fractionation of the total effluent. It consists of hydrogen, methane, ethane and propane.]\nH K\n270-999-8\n68513-14-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-146-00-2\nGases (petroleum), reformer effluent high-pressure flash drum off;\nRefinery gas;\n[A complex combination produced by the high-pressure flashing of the effluent from the reforming reactor. It consists primarily of hydrogen with various small amounts of methane, ethane, and propane.]\nH K\n271-003-4\n68513-18-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-147-00-8\nGases (petroleum), reformer effluent low-pressure flash drum off;\nRefinery gas;\n[A complex combination produced by low-pressure flashing of the effluent from the reforming reactor. It consists primarily of hydrogen with various small amounts of methane, ethane, and propane.]\nH K\n271-005-5\n68513-19-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-148-00-3\nGases (petroleum), oil refinery gas distn. off;\nRefinery gas;\n[A complex combination separated by distillation of a gas stream containing hydrogen, carbon monoxide, carbon dioxide and hydrocarbons having carbon numbers in the range of C1 through C6 or obtained by cracking ethane and propane. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C2, hydrogen, nitrogen, and carbon monoxide.]\nH K\n271-258-1\n68527-15-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-149-00-9\nGases (petroleum), benzene unit hydrotreater depentanizer overheads;\nRefinery gas;\n[A complex combination produced by treating the feed from the benzene unit with hydrogen in the presence of a catalyst followed by depentanizing. It consists primarily of hydrogen, ethane and propane with various small amounts of nitrogen, carbon monoxide, carbon dioxide and hydrocarbons having carbon numbers predominantly in the range of C1 through C6. It may contain trace amounts of benzene.]\nH K\n271-623-5\n68602-82-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-150-00-4\nGases (petroleum), secondary absorber off, fluidized catalytic cracker overheads fractionator;\nRefinery gas;\n[A complex combination produced by the fractionation of the overhead products from the catalytic cracking process in the fluidized catalytic cracker. It consists of hydrogen, nitrogen, and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.]\nH K\n271-625-6\n68602-84-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-151-00-X\nPetroleum products, refinery gases;\nRefinery gas;\n[A complex combination which consists primarily of hydrogen with various small amounts of methane, ethane, and propane.]\nH K\n271-750-6\n68607-11-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-152-00-5\nGases (petroleum), hydrocracking low-pressure separator;\nRefinery gas;\n[A complex combination obtained by the liquid-vapor separation of the hydrocracking process reactor effluent. It consists predominantly of hydrogen and saturated hydrocarbons having carbon numbers predominantly in the range of C1 through C3.]\nH K\n272-182-1\n68783-06-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-153-00-0\nGases (petroleum), refinery;\nRefinery gas;\n[A complex combination obtained from various petroleum refining operations. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C3.]\nH K\n272-338-9\n68814-67-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-154-00-6\nGases (petroleum), platformer products separator off;\nRefinery gas;\n[A complex combination obtained from the chemical reforming of naphthenes to aromatics. It consists of hydrogen and saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C4.]\nH K\n272-343-6\n68814-90-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-155-00-1\nGases (petroleum), hydrotreated sour kerosine depentanizer stabilizer off;\nRefinery gas;\n[The complex combination obtained from the depentanizer stabilization of hydrotreated kerosine. It consists primarily of hydrogen, methane, ethane, and propane with various small amounts of nitrogen, hydrogen sulfide, carbon monoxide and hydrocarbons having carbon numbers predominantly in the range of C4 through C5.]\nH K\n272-775-5\n68911-58-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-156-00-7\nGases (petroleum), hydrotreated sour kerosine flash drum;\nRefinery gas;\n[A complex combination obtained from the flash drum of the unit treating sour kerosine with hydrogen in the presence of a catalyst. It consists primarily of hydrogen and methane with various small amounts of nitrogen, carbon monoxide, and hydrocarbons having carbon numbers predominantly in the range of C2 through C5.]\nH K\n272-776-0\n68911-59-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-157-00-2\nGases (petroleum), distillate unifiner desulfurization stripper off;\nRefinery gas;\n[A complex combination stripped from the liquid product of the unifiner desulfurization process. It consists of hydrogen sulfide, methane, ethane, and propane.]\nH K\n272-873-8\n68919-01-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-158-00-8\nGases (petroleum), fluidized catalytic cracker fractionation off;\nRefinery gas;\n[A complex combination produced by the fractionation of the overhead product of the fluidized catalytic cracking process. It consists of hydrogen, hydrogen sulfide, nitrogen, and hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n272-874-3\n68919-02-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-159-00-3\nGases (petroleum), fluidized catalytic cracker scrubbing secondary absorber off;\nRefinery gas;\n[A complex combination produced by scrubbing the overhead gas from the fluidized catalytic cracker. It consists of hydrogen, nitrogen, methane, ethane and propane.]\nH K\n272-875-9\n68919-03-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-160-00-9\nGases (petroleum), heavy distillate hydrotreater desulfurization stripper off;\nRefinery gas;\n[A complex combination stripped from the liquid product of the heavy distillate hydrotreater desulfurization process. It consists of hydrogen, hydrogen sulfide, and saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n272-876-4\n68919-04-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-161-00-4\nGases (petroleum), platformer stabilizer off, light ends fractionation;\nRefinery gas;\n[A complex combination obtained by the fractionation of the light ends of the platinum reactors of the platformer unit. It consists of hydrogen, methane, ethane and propane.]\nH K\n272-880-6\n68919-07-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-162-00-X\nGases (petroleum), preflash tower off, crude distn.;\nRefinery gas;\n[A complex combination produced from the first tower used in the distillation of crude oil. It consists of nitrogen and saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n272-881-1\n68919-08-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-163-00-5\nGases (petroleum), tar stripper off;\nRefinery gas;\n[A complex combination obtained by the fractionation of reduced crude oil. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n272-884-8\n68919-11-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-164-00-0\nGases (petroleum), unifiner stripper off;\nRefinery gas;\n[A combination of hydrogen and methane obtained by fractionation of the products from the unifiner unit.]\nH K\n272-885-3\n68919-12-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-165-00-6\nTail gas (petroleum), catalytic hydrodesulfurized naphtha separator;\nRefinery gas;\n[A complex combination of hydrocarbons obtained from the hydrodesulfurization of naphtha. It consists of hydrogen, methane, ethane, and propane.]\nH K\n273-173-5\n68952-79-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-166-00-1\nTail gas (petroleum), straight-run naphtha hydrodesulfurizer;\nRefinery gas;\n[A complex combination obtained from the hydrodesulfurization of straight-run naphtha. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n273-174-0\n68952-80-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-167-00-7\nGases (petroleum), sponge absorber off, fluidized catalytic cracker and gas oil desulfurizer overhead fractionation;\nRefinery gas;\n[A complex combination obtained by the fractionation of products from the fluidized catalytic cracker and gas oil desulfurizer. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n273-269-7\n68955-33-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-168-00-2\nGases (petroleum), crude distn. and catalytic cracking;\nRefinery gas;\n[A complex combination produced by crude distillation and catalytic cracking processes. It consists of hydrogen, hydrogen sulfide, nitrogen, carbon monoxide and paraffinic and olefinic hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n273-563-5\n68989-88-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-169-00-8\nGases (petroleum), gas oil diethanolamine scrubber off;\nRefinery gas;\n[A complex combination produced by desulfurization of gas oils with diethanolamine. It consists predominantly of hydrogen sulfide, hydrogen and aliphatic hydrocarbons having carbon numbers in the range of C1 through C5.]\nH K\n295-397-2\n92045-15-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-170-00-3\nGases (petroleum), gas oil hydrodesulfurization effluent;\nRefinery gas;\n[A complex combination obtained by separation of the liquid phase from the effluent from the hydrogenation reaction. It consists predominantly of hydrogen, hydrogen sulfide and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C3.]\nH K\n295-398-8\n92045-16-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-171-00-9\nGases (petroleum), gas oil hydrodesulfurization purge;\nRefinery gas;\n[A complex combination of gases obtained from the reformer and from the purges from the hydrogenation reactor. It consists predominantly of hydrogen and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n295-399-3\n92045-17-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-172-00-4\nGases (petroleum), hydrogenator effluent flash drum off;\nRefinery gas;\n[A complex combination of gases obtained from flash of the effluents after the hydrogenation reaction. It consists predominantly of hydrogen and aliphatic hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n295-400-7\n92045-18-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-173-00-X\nGases (petroleum), naphtha steam cracking high-pressure residual;\nRefinery gas;\n[A complex combination obtained as a mixture of the non-condensable portions from the product of a naphtha steam cracking process as well as residual gases obtained during the preparation of subsequent products. It consists predominantly of hydrogen and paraffinic and olefinic hydrocarbons having carbon numbers predominantly in the range of C1 through C5 with which natural gas may also be mixed.]\nH K\n295-401-2\n92045-19-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-174-00-5\nGases (petroleum), residue visbaking off;\nRefinery gas;\n[A complex combination obtained from viscosity reduction of residues in a furnace. It consists predominantly of hydrogen sulfide and paraffinic and olefinic hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n295-402-8\n92045-20-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-177-00-1\nGases (petroleum), C3-4;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by distillation of products from the cracking of crude oil. It consists of hydrocarbons having carbon numbers in the range of C3 through C4, predominantly of propane and propylene, and boiling in the range of approximately -51 °C to -1 °C (-60 °F to 30 °F.)]\nH K\n268-629-5\n68131-75-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-178-00-7\nTail gas (petroleum), catalytic cracked distillate and catalytic cracked naphtha fractionation absorber;\nPetroleum gas;\n[The complex combination of hydrocarbons from the distillation of the products from catalytic cracked distillates and catalytic cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C1 through C4.]\nH K\n269-617-2\n68307-98-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-179-00-2\nTail gas (petroleum), catalytic polymn. naphtha fractionation stabilizer;\nPetroleum gas;\n[A complex combination of hydrocarbons from the fractionation stabilization products from polymerization of naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C1 through C4.]\nH K\n269-618-8\n68307-99-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-180-00-8\nTail gas (petroleum), catalytic reformed naphtha fractionation stabilizer, hydrogen sulfide-free;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from fractionation stabilization of catalytic reformed naphtha and from which hydrogen sulfide has been removed by amine treatment. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n269-619-3\n68308-00-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-181-00-3\nTail gas (petroleum), cracked distillate hydrotreater stripper;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by treating thermal cracked distillates with hydrogen in the presence of a catalyst. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n269-620-9\n68308-01-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-182-00-9\nTail gas (petroleum), straight-run distillate hydrodesulfurizer, hydrogen sulfide-free;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from catalytic hydrodesulfurization of straight run distillates and from which hydrogen sulfide has been removed by amine treatment. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n269-630-3\n68308-10-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-183-00-4\nTail gas (petroleum), gas oil catalytic cracking absorber;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the distillation of products from the catalytic cracking of gas oil. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n269-623-5\n68308-03-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-184-00-X\nTail gas (petroleum), gas recovery plant;\nPetroleum gas;\n[A complex combination of hydrocarbons from the distillation of products from miscellaneous hydrocarbon streams. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n269-624-0\n68308-04-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-185-00-5\nTail gas (petroleum), gas recovery plant deethanizer;\nPetroleum gas;\n[A complex combination of hydrocarbons from the distillation of products from miscellaneous hydrocarbon streams. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n269-625-6\n68308-05-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-186-00-0\nTail gas (petroleum), hydrodesulfurized distillate and hydrodesulfurized naphtha fractionator, acid-free;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from fractionation of hydrodesulfurized naphtha and distillate hydrocarbon streams and treated to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n269-626-1\n68308-06-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-187-00-6\nTail gas (petroleum), hydrodesulfurized vacuum gas oil stripper, hydrogen sulfide-free;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from stripping stabilization of catalytic hydrodesulfurized vacuum gas oil and from which hydrogen sulfide has been removed by amine treatment. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n269-627-7\n68308-07-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-188-00-1\nTail gas (petroleum), light straight-run naphtha stabilizer, hydrogen sulfide-free;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from fractionation stabilization of light straight run naphtha and from which hydrogen sulfide has been removed by amine treatment. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH K\n269-629-8\n68308-09-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-189-00-7\nTail gas (petroleum), propane-propylene alkylation feed prep deethanizer;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the distillation of the reaction products of propane with propylene. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n269-631-9\n68308-11-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-190-00-2\nTail gas (petroleum), vacuum gas oil hydrodesulfurizer, hydrogen sulfide-free;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from catalytic hydrodesulfurization of vacuum gas oil and from which hydrogen sulfide has been removed by amine treatment. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C6.]\nH K\n269-632-4\n68308-12-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-191-00-8\nGases (petroleum), catalytic cracked overheads;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of products from the catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C5 and boiling in the range of approximately -48 °C to 32 °C (-54 °F to 90 °F).]\nH K\n270-071-2\n68409-99-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-193-00-9\nAlkanes, C1-2;\nPetroleum gas\nH K\n270-651-5\n68475-57-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-194-00-4\nAlkanes, C2-3;\nPetroleum gas\nH K\n270-652-0\n68475-58-1\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-195-00-X\nAlkanes, C3-4;\npetroleum gas\nH K\n270-653-6\n68475-59-2\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-196-00-5\nAlkanes, C4-5;\nPetroleum gas\nH K\n270-654-1\n68475-60-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-197-00-0\nFuel gases;\nPetroleum gas;\n[A combination of light gases. It consists predominantly of hydrogen and/or low molecular weight hydrocarbons.]\nH K\n270-667-2\n68476-26-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-198-00-6\nFuel gases, crude oil of distillates;\nPetroleum gas;\n[A complex combination of light gases produced by distillation of crude oil and by catalytic reforming of naphtha. It consists of hydrogen and hydrocarbons having carbon numbers predominantly in the range of C1 through C4 and boiling in the range of approximately -217 °C to -12 °C (-423 °F to 10 °F).]\nH K\n270-670-9\n68476-29-9\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-199-00-1\nHydrocarbons, C3-4;\nPetroleum gas\nH K\n270-681-9\n68476-40-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-200-00-5\nHydrocarbons, C4-5;\nPetroleum gas\nH K\n270-682-4\n68476-42-6\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-201-00-0\nHydrocarbons, C2-4, C3-rich;\nPetroleum gas\nH K\n270-689-2\n68476-49-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-202-00-6\nPetroleum gases, liquefied;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately -40 °C to 80 °C (-40 °F to 176 °F).]\nHKS\n270-704-2\n68476-85-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-203-00-1\nPetroleum gases, liquefied, sweetened;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained by subjecting liquefied petroleum gas mix to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C7 and boiling in the range of approximately -40 °C to 80 °C (-40 °F to 176 °F).]\nHKS\n270-705-8\n68476-86-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-204-00-7\ngases (petroleum), C3-4, isobutane-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons from the distillation of saturated and unsaturated hydrocarbons usually ranging in carbon numbers from C3 through C6, predominantly butane and isobutane. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C4, predominantly isobutane.]\nH K\n270-724-1\n68477-33-8\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-205-00-2\nDistillates (petroleum), C3-6, piperylene-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons from the distillation of saturated and unsaturated aliphatic hydrocarbons usually ranging in the carbon numbers C3 through C6. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C6, predominantly piperylenes.]\nH K\n270-726-2\n68477-35-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-206-00-8\nGases (petroleum), butane splitter overheads;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the distillation of the butane stream. It consists of aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C4.]\nH K\n270-750-3\n68477-69-0\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-207-00-3\nGases (petroleum), C2-3;\nPetroleum gas;\n[A complex combination of hydrocarbons produced by the distillation of products from a catalytic fractionation process. It contains predominantly ethane, ethylene, propane, and propylene.]\nH K\n270-751-9\n68477-70-3\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-208-00-9\nGases (petroleum), catalytic-cracked gas oil depropanizer bottoms, C4-rich acid-free;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from fractionation of catalytic cracked gas oil hydrocarbon stream and treated to remove hydrogen sulfide and other acidic components. It consists of hydrocarbons having carbon numbers in the range of C3 through C5, predominantly C4.]\nH K\n270-752-4\n68477-71-4\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-209-00-4\nGases (petroleum), catalytic-cracked naphtha debutanizer bottoms, C3-5-rich;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the stabilization of catalytic cracked naphtha. It consists of aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C5.]\nH K\n270-754-5\n68477-72-5\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-210-00-X\nTail gas (petroleum), isomerized naphtha fractionation stabilizer;\nPetroleum gas;\n[A complex combination of hydrocarbons obtained from the fractionation stabilization products from isomerized naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C1 through C4.]\nH K\n269-628-2\n68308-08-7\nF+; R12\nCarc. Cat. 1; R45\nMuta. Cat. 2; R46\nF+; T\nR: 45-46-12\nS: 53-45\n649-261-00-8\nGasoline, natural;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons separated from natural gas by processes such as refrigeration or absorption. It consists predominantly of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately minus 20 °C to 120 °C (-4 °F to 248 °F).]\nH P\n232-349-1\n8006-61-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-262-00-3\nNaphtha;\nLow boiling point naphtha;\n[Refined, partly refined, or unrefined petroleum products produced by the distillation of natural gas. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C6 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).]\nH P\n232-443-2\n8030-30-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-263-00-9\nLigroine;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons obtained by the fractional distillation of petroleum. This fraction boils in a range of approximately 20 °C to 135 °C (58 °F to 275 °F).]\nH P\n232-453-7\n8032-32-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-264-00-4\nNaphtha (petroleum), heavy straight-run;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).]\nH P\n265-041-0\n64741-41-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C <10 %: T; R45-46\n4\n649-265-00-X\nNaphtha (petroleum), full-range straight-run;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons produced by distillation of crude oil. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately -20 °C to 220 °C (-4 °F to 428 °F).]\nH P\n265-042-6\n64741-42-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-266-00-5\nNaphtha (petroleum), light straight-run;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons produced by distillation of crude oil. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately -20 °C to 180 °C (-4 °F to 356 °F).]\nH P\n265-046-8\n64741-46-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-267-00-0\nSolvent naphtha (petroleum), light aliph.;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons obtained from the distillation of crude oil or natural gasoline. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C5 through C10 and boiling in the range of approximately 35 °C to 160 °C (95 °F to 320 °F).]\nH P\n265-192-2\n64742-89-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-268-00-6\nDistillates (petroleum), straight-run light;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons produced by the distillation of crude oil It consists of hydrocarbons having carbon numbers predominantly in the range of C2 through C7 and boiling in the range of approximately -88 °C to 99 °C (-127 °F to 210 °F).]\nH P\n270-077-5\n68410-05-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-269-00-1\nGasoline, vapor-recovery;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons separated from the gases from vapor recovery systems by cooling. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately -20 °C to 196 °C(-4 °F to 384 °F).]\nH P\n271-025-4\n68514-15-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-270-00-7\nGasoline, straight-run, topping-plant;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons produced from the topping plant by the distillation of crude oil. It boils in the range of approximately 36.1 °C to 193.3 °C (97 °F to 380 °F).]\nH P\n271-727-0\n68606-11-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 ≤ C < 10 %: T; R45-46\n4\n649-271-00-2\nNaphtha (petroleum), unsweetened;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons produced from the distillation of naphtha streams from various refinery processes It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 0 °C to 230 °C (25 °F to 446 °F).]\nH P\n272-186-3\n68783-12-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-272-00-8\nDistillates (petroleum), light straight-run gasoline fractionation stabilizer overheads;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons obtained by the fractionation of light straight-run gasoline. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C6.]\nH P\n272-931-2\n68921-08-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-273-00-3\nNaphtha (petroleum), heavy straight run, arom.-contg.;\nLow boiling point naphtha;\n[A complex combination of hydrocarbons obtained from a distillation process of crude petroleum. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).]\nH P\n309-945-6\n101631-20-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-274-00-9\nNaphtha (petroleum), full-range alkylate;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 220 °C (194 °F to 428 °F).]\nH P\n265-066-7\n64741-64-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-275-00-4\nNaphtha (petroleum), heavy alkylate;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 to C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C9 through C12 and boiling in the range of approximately 150 °C to 220 °C (302 °F to 428 °F).]\nH P\n265-067-2\n64741-65-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-276-00-X\nNaphtha (petroleum), light alkylate;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons produced by distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C10 and boiling in the range of approximately 90 °C to 160 °C (194 °F to 320 °F).]\nH P\n265-068-8\n64741-66-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-277-00-5\nNaphtha (petroleum), isomerization;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons obtained from catalytic isomerization of straight chain paraffinic C4 through C6 hydrocarbons. It consists predominantly of saturated hydrocarbons such as isobutane, isopentane, 2,2-dimethylbutane, 2-methylpentane, and 3-methylpentane.]\nH P\n265-073-5\n64741-70-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-278-00-0\nNaphtha (petroleum), solvent-refined light;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).]\nH P\n265-086-6\n64741-84-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-279-00-6\nNaphtha (petroleum), solvent-refined heavy;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons obtained as the raffinate from a solvent extraction process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).]\nH P\n265-095-5\n64741-92-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-280-00-1\nRaffinates (petroleum), catalytic reformer ethylene glycol-water countercurrent exts.;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons obtained as the raffinate from the UDEX extraction process on the catalytic reformer stream. It consists of saturated hydrocarbons having carbon numbers predominantly in the range of C6 through C9.]\nH P\n270-088-5\n68410-71-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-281-00-7\nRaffinates (petroleum), reformer, Lurgi unit-sepd.;\nLow boiling point modified naphtha;\n[The complex combination of hydrocarbons obtained as a raffinate from a Lurgi separation unit. It consists predominantly of non-aromatic hydrocarbons with various small amounts of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8.]\nH P\n270-349-3\n68425-35-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-282-00-2\nNaphtha (petroleum), full-range alkylate, butane-contg.;\nLow boiling point modified naphta;\n[A complex combination of hydrocarbons produced by the distillation of the reaction products of isobutane with monoolefinic hydrocarbons usually ranging in carbon numbers from C3 through C5. It consists of predominantly branched chain saturated hydrocarbons having carbon numbers predominantly in the range of C7 through C12 with some butanes and boiling in the range of approximately 35 °C to 200 °C (95 °F to 428 °F).]\nH P\n271-267-0\n68527-27-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-283-00-8\nDistillates (petroleum), naphtha steam cracking-derived, solvent-refined light hydrotreated;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons obtained as the raffinates from a solvent extraction process of hydrotreated light distillate from steam-cracked naphtha.]\nH P\n295-315-5\n91995-53-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-284-00-3\nNaphtha (petroleum), C4-12 butane-alkylate, isooctane-rich;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons obtained by alkylation of butanes. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12, rich in isooctane, and boiling in the range of approximately 35 °C to 210 °C (95 °F to 410 °F).]\nH P\n295-430-0\n92045-49-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-285-00-9\nHydrocarbons, hydrotreated light naphtha distillates, solvent-refined;\nLow boiling point modified naphtha;\n[A combination of hydrocarbons obtained from the distillation of hydrotreated naphtha followed by a solvent extraction and distillation process. It consists predominantly of saturated hydrocarbons boiling in the range of approximately 94 °C to 99 °C (201 °F to 210 °F).]\nH P\n295-436-3\n92045-55-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-286-00-4\nNaphtha (petroleum), isomerization, C6-fraction;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons obtained by distillation of a gasoline which has been catalytically isomerized. It consists predominantly of hexane isomers boiling in the range of approximately 60 °C to 66 °C (140 °F to 151 °F).]\nH P\n295-440-5\n92045-58-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-287-00-X\nHydrocarbons, C6-7, naphtha-cracking, solvent-refined;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons obtained by the sorption of benzene from a catalytically fully hydrogenated benzene-rich hydrocarbon cut that was distillatively obtained from prehydrogenated cracked naphtha. It consists predominantly of paraffinic and naphthenic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 70 °C to 100 °C (158 °F to 212 °F).]\nH P\n295-446-8\n92045-64-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-288-00-5\nHydrocarbons, C6-rich, hydrotreated light naphtha distillates, solvent-refined;\nLow boiling point modified naphtha;\n[A complex combination of hydrocarbons obtained by distillation of hydrotreated naphtha followed by solvent extraction. It consists predominantly of saturated hydrocarbons and boiling in the range of approximately 65 °C to 70 °C (149 °F to 158 °F).]\nH P\n309-871-4\n101316-67-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-289-00-0\nNaphtha (petroleum), heavy catalytic cracked;\nLow boiling point cat-cracked naphtha;\n[A complex combination of hydrocarbons produced by a distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (148 °F to 446 °F). It contains a relatively large proportion of unsaturated hydrocarbons.]\nH P\n265-055-7\n64741-54-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-290-00-6\nNaphtha (petroleum), light catalytic cracked;\nLow boiling point cat-cracked naphtha;\n[A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately -20 °C to 190 °C (-4 °F to 374 °F). It contains a relatively large proportion of unsaturated hydrocarbons.]\nH P\n265-056-2\n64741-55-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-291-00-1\nHydrocarbons, C3-11, catalytic cracker distillates;\nLow boiling point cat-cracked naphtha;\n[A complex combination of hydrocarbons produced by the distillations of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C11 and boiling in a range approximately up to 204 °C (400 °F).]\nH P\n270-686-6\n68476-46-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-292-00-7\nNaphtha (petroleum), catalytic cracked light distd.;\nLow boiling point cat-cracked naphtha;\n[A complex combination of hydrocarbons produced by the distillation of products from a catalytic cracking process. It consists of hydrocarbons having carbon numbers predominantly in the range of C1 through C5.]\nH P\n272-185-8\n68783-09-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-293-00-2\nDistillates (petroleum), naphtha steam cracking-derived, hydrotreated light arom.;\nLow boiling point cat-cracked naphtha.;\n[A complex combination of hydrocarbons obtained by treating a light distillate from steam-cracked naphtha. It consists predominantly of aromatic hydrocarbons.]\nH P\n295-311-3\n91995-50-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-294-00-8\nNaphtha (petroleum), heavy catalytic cracked, sweetened;\nLow boiling point cat-cracked naphtha;\n[A complex combination of hydrocarbons obtained by subjecting a catalytic cracked petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 60 °C to 200 °C (140 °F to 392 °F).]\nH P\n295-431-6\n92045-50-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-295-00-3\nNaphtha (petroleum), light catalytic cracked sweetened;\nLow boiling point cat-cracked naphtha;\n[A complex combination of hydrocarbons obtained by subjecting naphtha from a catalytic cracking process to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons boiling in a range of approximately 35 °C to 210 °C (95 °F to 410 °F).]\nH P\n295-441-0\n92045-59-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-296-00-9\nHydrocarbons, C8-12, catalytic-cracking, chem. neutralized;\nLow boiling point cat-cracked naphtha;\n[A complex combination of hydrocarbons produced by the distillation of a cut from the catalytic cracking process, having undergone an alkaline washing. It consists predominantly of hydrocarbons having carbon numbers in the range of C8 through C12 and boiling in the range of approximately 130 °C to 210 °C (266 °F to 410 °F).]\nH P\n295-794-0\n92128-94-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-297-00-4\nHydrocarbons, C8-12, catalytic cracker distillates;\nLow boiling point cat-cracked naphtha;\n[A complex combination of hydrocarbons obtained by distillation of products from a catalytic cracking process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C12 and boiling in the range of approximately 140 °C to 210 °C (284 °F to 410 °F).]\nH P\n309-974-4\n101794-97-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-298-00-X\nHydrocarbons, C8-12, catalytic cracking, chem. neutralized, sweetened;\nLow boiling point cat-cracked naphtha\nH P\n309-987-5\n101896-28-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-299-00-5\nNaphtha (petroleum), light catalytic reformed;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.]\nH P\n265-065-1\n64741-63-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-300-00-9\nNaphtha (petroleum), heavy catalytic reformed;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons produced from the distillation of products from a catalytic reforming process. It consists of predominantly aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).]\nH P\n265-070-9\n64741-68-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-301-00-4\nDistillates (petroleum), catalytic reformed depentanizer;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons from the distillation of products from a catalytic reforming process. It consists predominantly of aliphatic hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately -49 °C to 63 °C (-57 °F to 145 °F).]\nH P\n270-660-4\n68475-79-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-302-00-X\nHydrocarbons, C2-6, C6-8 catalytic reformer;\nLow boiling point cat-reformed naphtha\nH P\n270-687-1\n68476-47-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-303-00-5\nResidues (petroleum), C6-8 catalytic reformer;\nLow boiling point cat-reformed naphtha;\n[A complex residuum from the catalytic reforming of C6-8 feed. It consists of hydrocarbons having carbon numbers predominantly in the range of C2 through C6.]\nH P\n270-794-3\n68478-15-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-304-00-0\nNaphtha (petroleum), light catalytic reformed, arom.-free;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons obtained from distillation of products from a catalytic reforming process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 35 °C to 120 °C (95 °F to 248 °F). It contains a relatively large proportion of branched chain hydrocarbons with the aromatic components removed.]\nH P\n270-993-5\n68513-03-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-305-00-6\nDistillates (petroleum), catalytic reformed straight-run naphtha overheads;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons obtained by the catalytic reforming of straight-run naphtha followed by the fractionation of the total effluent. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C6.]\nH P\n271-008-1\n68513-63-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-306-00-1\nPetroleum products, hydrofiner-powerformer reformates;\nLow boiling point cat-reformed naphtha;\n[The complex combination of hydrocarbons obtained in a hydrofiner-powerformer process and boiling in a range of approximately 27 °C to 210 °C (80 °F to 410 °F).]\nH P\n271-058-4\n68514-79-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-307-00-7\nNaphtha (petroleum), full-range reformed;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons produced by the distillation of the products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).]\nH P\n272-895-8\n68919-37-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C <10 %: T; R45-46\n4\n649-308-00-2\nNaphtha (petroleum), catalytic reformed;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons produced by the distillation of products from a catalytic reforming process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 220 °C (90 °F to 430 °F). It contains a relatively large proportion of aromatic and branched chain hydrocarbons. This stream may contain 10 vol. % or more benzene.]\nH P\n273-271-8\n68955-35-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-309-00-8\nDistillates (petroleum), catalytic reformed hydrotreated light, C8-12 arom. fraction;\nLow boiling point cat-reformed naphtha;\n[A complex combination of alkylbenzenes obtained by the catalytic reforming of petroleum naphtha. It consists predominantly of alkylbenzenes having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 160 °C to 180 °C (320 °F to 356 °F).]\nH P\n285-509-8\n85116-58-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-310-00-3\nAromatic hydrocarbons, C8, catalytic reforming-derived;\nLow boiling point cat-reformed naphtha\nH P\n295-279-0\n91995-18-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-311-00-9\nAromatic hydrocarbons, C7-12, C8-rich;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 (primarily C8) and can contain nonaromatic hydrocarbons, both boiling in the range of approximately 130 °C to 200 °C (266 °F to 392 °F).]\nH P\n297-401-8\n93571-75-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-312-00-4\nGasoline, C5-11, high-octane stabilized reformed;\nLow boiling point cat-reformed naphtha;\n[A complex high octane combination of hydrocarbons obtained by the catalytic dehydrogenation of a predominantly naphthenic naphtha. It consists predominantly of aromatics and non-aromatics having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 45 °C to 185 °C (113 °F to 365 °F).]\nH P\n297-458-9\n93572-29-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-313-00-X\nHydrocarbons, C7-12, C >9-arom.-rich, reforming heavy fraction;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 120 °C to 210 °C (248 °F to 380 °F) and C9 and higher aromatic hydrocarbons.]\nH P\n297-465-7\n93572-35-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-314-00-5\nHydrocarbons, C5-11, nonaroms.-rich, reforming light fraction;\nLow boiling point cat-reformed naphtha;\n[A complex combination of hydrocarbons obtained by separation from the platformate-containing fraction. It consists predominantly of nonaromatic hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 125 °C (94 °F to 257 °F), benzene and toluene.]\nH P\n297-466-2\n93572-36-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-316-00-6\nNaphtha (petroleum), light thermal cracked;\nLow boiling point thermally cracked naphtha;\n[A complex combination of hydrocarbons from distillation of products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C8 and boiling in the range of approximately -10 °C to 130 °C (14 °F to 266 °F).]\nH P\n265-075-6\n64741-74-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-317-00-1\nNaphtha (petroleum), heavy thermal cracked;\nLow boiling point thermally cracked naphtha;\n[A complex combination of hydrocarbons from distillation of the products from a thermal cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 220 °C (148 °F to 428 °F).]\nH P\n265-085-0\n64741-83-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-318-00-7\nDistillates (petroleum), heavy arom.;\nLow boiling point thermally cracked naphtha;\n[The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This higher boiling fraction consists predominantly of C5-7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having carbon number predominantly of C5.This stream may contain benzene.]\nH P\n267-563-4\n67891-79-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-319-00-2\nDistillates (petroleum), light arom.;\nLow boiling point thermally cracked naphtha;\n[The complex combination of hydrocarbons from the distillation of the products from the thermal cracking of ethane and propane. This lower boiling fraction consists predominantly of C5-7 aromatic hydrocarbons with some unsaturated aliphatic hydrocarbons having a carbon number predominantly of C5.This stream may contain benzene.]\nH P\n267-565-5\n67891-80-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-320-00-8\nDistillates (petroleum), naphtha-raffinate pyrolyzate-derived, gasoline-blending;\nLow boiling point thermally cracked naphtha;\n[The complex combination of hydrocarbons obtained by the pyrolysis fractionation at 816 °C (1 500 °F) of naphtha and raffinate. It consists predominantly of hydrocarbons having a carbon number of C9 and boiling at approximately 204 °C (400 °F).]\nH P\n270-344-6\n68425-29-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-321-00-3\nAromatic hydrocarbons, C6-8, naphtha-raffinate pyrolyzate-derived;\nLow boiling point thermally cracked naphtha;\n[A complex combination of hydrocarbons obtained by the fractionation pyrolysis at 816 °C (1 500 °F) of naphtha and raffinate. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C6 through C8, including benzene.]\nH P\n270-658-3\n68475-70-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-322-00-9\nDistillates (petroleum), thermal cracked naphtha and gas oil;\nLow boiling point thermally cracked naphtha;\n[A complex combination of hydrocarbons produced by distillation of thermally cracked naphtha and/or gas oil. It consists predominantly of olefinic hydrocarbons having a carbon number of C5 and boiling in the range of approximately 33 °C to 60 °C (91 °F to 140 °F).]\nH P\n271-631-9\n68603-00-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-323-00-4\nDistillates (petroleum), thermal cracked naphtha and gas oil, C5-dimer-contg.;\nLow boiling point thermally cracked naphtha;\n[A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil. It consists predominantly of hydrocarbons having a carbon number of C5 with some dimerized C5 olefins and boiling in the range of approximately 33 °C to 184 °C (91 °F to 363 °F).]\nH P\n271-632-4\n68603-01-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-324-00-X\nDistillates (petroleum), thermal cracked naphtha and gas oil, extractive;\nLow boiling point thermally cracked naphtha;\n[A complex combination of hydrocarbons produced by the extractive distillation of thermal cracked naphtha and/or gas oil.. It consists of paraffinic and olefinic hydrocarbons, predominantly isoamylenes such as 2-methyl-1-butene and 2-methyl-2-butene and boiling in the range of approximately 31 °C to 40 °C (88 °F to 104 °F).]\nH P\n271-634-5\n68603-03-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-325-00-5\nDistillates (petroleum), light thermal cracked, debutanized arom.;\nLow boiling point thermally cracked naphtha;\n[A complex combination of hydrocarbons produced by the distillation of products from a thermal cracking process. It consists predominantly of aromatic hydrocarbons, primarily benzene.]\nH P\n273-266-0\n68955-29-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 %≤ C <10 %: T; R45-46\n4\n649-326-00-0\nNaphtha (petroleum), light thermal cracked, sweetened;\nLow boiling point thermally cracked naphtha;\n[A complex combination of hydrocarbons obtained by subjecting a petroleum distillate from the high temperature thermal cracking of heavy oil fractions to a sweetening process to convert mercaptans. It consists predominantly of aromatics, olefins and saturated hydrocarbons boiling in the range of approximately 20 °C to 100 °C (68 °F to 212 °F).]\nH P\n295-447-3\n92045-65-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-327-00-6\nNaphtha (petroleum), hydrotreated heavy;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C13 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).]\nH P\n265-150-3\n64742-48-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-328-00-1\nNaphtha (petroleum), hydrotreated light;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (-4 °F to 374 °F).]\nH P\n265-151-9\n64742-49-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-329-00-7\nNaphtha (petroleum), hydrodesulfurized light;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately -20 °C to 190 °C (-4 °F to 374 °F).]\nH P\n265-178-6\n64742-73-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-330-00-2\nNaphtha (petroleum), hydrodesulfurized heavy;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).]\nH P\n265-185-4\n64742-82-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-331-00-8\nDistillates (petroleum), hydrotreated middle, intermediate boiling;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by the distillation of products from a middle distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C5 through C10 and boiling in the range of approximately 127 °C to 188 °C (262 °F to 370 °F).]\nH P\n270-092-7\n68410-96-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-332-00-3\nDistillates (petroleum), light distillate hydrotreating process, low-boiling;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by the distillation of products from the light distillate hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C9 and boiling in the range of approximately 3 °C to 194 °C (37 °F to 382 °F).]\nH P\n270-093-2\n68410-97-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-333-00-9\nDistillates (petroleum), hydrotreated heavy naphtha, deisohexanizer overheads;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by distillation of the products from a heavy naphtha hydrotreating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately -49 °C to 68 °C (-57 °F to 155 °F).]\nH P\n270-094-8\n68410-98-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 %≤ C <10 %: T; R45-46\n4\n649-334-00-4\nSolvent naphtha (petroleum), light arom., hydrotreated;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).]\nH P\n270-988-8\n68512-78-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-335-00-X\nNaphtha (petroleum), hydrodesulfurized thermal cracked light;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by fractionation of hydrodesulfurized thermal cracker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 195 °C (73 °F to 383 °F).]\nH P\n285-511-9\n85116-60-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-336-00-5\nNaphtha (petroleum), hydrotreated light, cycloalkane-contg.;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained from the distillation of a petroleum fraction. It consists predominantly of alkanes and cycloalkanes boiling in the range of approximately -20 °C to 190 °C (-4 °F to 374 °F).]\nH P\n285-512-4\n85116-61-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-337-00-0\nNaphtha (petroleum), heavy steam-cracked, hydrogenated;\nLow boiling point hydrogen treated naphtha\nH P\n295-432-1\n92045-51-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-338-00-6\nNaphtha (petroleum), hydrodesulfurized full-range;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained from a catalytic hydrodesulfurization process. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 250 °C (86 °F to 482 °F).]\nH P\n295-433-7\n92045-52-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-339-00-1\nNaphtha (petroleum), hydrotreated light steam-cracked;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by treating a petroleum fraction, derived from a pyrolysis process, with hydrogen in the presence of a catalyst. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C5 through C11 and boiling in the range of approximately 35 °C to 190 °C (95 °F to 374 °F).]\nH P\n295-438-4\n92045-57-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-340-00-7\nHydrocarbons, C4-12, naphtha-cracking, hydrotreated;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by distillation from the product of a naphtha steam cracking process and subsequent catalytic selective hydrogenation of gum formers. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 30 °C to 230 °C (86 °F to 446 °F).]\nH P\n295-443-1\n92045-61-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-341-00-2\nSolvent naphtha (petroleum), hydrotreated light naphthenic;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained by treating a petroleum fraction with hydrogen in the presence of a catalyst. It consists predominantly of cycloparaffinic hydrocarbons having carbon numbers predominantly in the range of C6 through C7 and boiling in the range of approximately 73 °C to 85 °C (163 °F to 185 °F).]\nH P\n295-529-9\n92062-15-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-342-00-8\nNaphtha (petroleum), light steam-cracked, hydrogenated;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons produced from the separation and subsequent hydrogenation of the products of a steam-cracking process to produce ethylene. It consists predominantly of saturated and unsaturated paraffins, cyclic paraffins and cyclic aromatic hydrocarbons having carbon numbers predominantly in the range of C4 through C10 and boiling in the range of approximately 50 °C to 200 °C (122 °F to 392 °F).The proportion of benzene hydrocarbons may vary up to 30 wt. % and the stream may also contain small amounts of sulfur and oxygenated compounds.]\nH P\n296-942-7\n93165-55-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-343-00-3\nHydrocarbons, C6-11, hydrotreated, dearomatized;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained as solvents which have been subjected to hydrotreatment in order to convert aromatics to naphthenes by catalytic hydrogenation.]\nH P\n297-852-0\n93763-33-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-344-00-9\nHydrocarbons, C9-12, hydrotreated, dearomatized;\nLow boiling point hydrogen treated naphtha;\n[A complex combination of hydrocarbons obtained as solvents which have been subjected to hydrotreatment in order to convert aromatics to naphthenes by catalytic hydrogenation.]\nH P\n297-853-6\n93763-34-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-345-00-4\nStoddard solvent;\nLow boiling point naphtha — unspecified;\n[A colorless, refined petroleum distillate that is free from rancid or objectionable odors and that boils in a range of approximately 148.8 °C to 204.4 °C. (300 °F to 400 °F).]\nH P\n232-489-3\n8052-41-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-346-00-X\nNatural gas condensates (petroleum);\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons separated as a liquid from natural gas in a surface separator by retrograde condensation. It consists mainly of hydrocarbons having carbon numbers predominantly in the range of C2 to C20. It is a liquid at atmospheric temperature and pressure.]\nH P\n265-047-3\n64741-47-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 %≤ C <10 %: T; R45-46\n4\n649-347-00-5\nNatural gas (petroleum), raw liq. mix;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons separated as a liquid from natural gas in a gas recycling plant by processes such as refrigeration or absorption. It consists mainly of saturated aliphatic hydrocarbons having carbon numbers in the range of C2 through C8.]\nH P\n265-048-9\n64741-48-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-348-00-0\nNaphtha (petroleum), light hydrocracked;\nLow boiling naphtha — unspecified;\n[A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C4 through C10, and boiling in the range of approximately -20 °C to 180 °C (-4 °F to 356 °F).]\nH P\n265-071-4\n64741-69-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-349-00-6\nNaphtha (petroleum), heavy hydrocracked;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons from distillation of the products from a hydrocracking process. It consists predominantly of saturated hydrocarbons having carbon numbers predominantly in the range of C6 through C12, and boiling in the range of approximately 65 °C to 230 °C (148 °F to 446 °F).]\nH P\n265-079-8\n64741-78-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-350-00-1\nNaphtha (petroleum), sweetened;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately -10 °C to 230 °C (14 °F to 446 °F).]\nH P\n265-089-2\n64741-87-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-351-00-7\nNaphtha (petroleum), acid-treated;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained as a raffinate from a sulfuric acid treating process. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 90 °C to 230 °C (194 °F to 446 °F).]\nH P\n265-115-2\n64742-15-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-352-00-2\nNaphtha (petroleum), chemically neutralized heavy;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C6 through C12 and boiling in the range of approximately 65 °C to 230 °C (149 °F to 446 °F).]\nH P\n265-122-0\n64742-22-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-353-00-8\nNaphtha (petroleum), chemically neutralized light;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons produced by a treating process to remove acidic materials. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately -20 °C to 190 °C (-4 °F to 374 °F).]\nH P\n265-123-6\n64742-23-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-354-00-3\nNaphtha (petroleum), catalytic dewaxed;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained from the catalytic dewaxing of a petroleum fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C12 and boiling in the range of approximately 35 °C to 230 °C (95 °F to 446 °F).]\nH P\n265-170-2\n64742-66-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-355-00-9\nNaphtha (petroleum), light steam-cracked;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by the distillation of the products from a steam cracking process. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately minus 20 °C to 190 °C (-4 °F to 374 °F).This stream is likely to contain 10 vol. % or more benzene.]\nH P\n265-187-5\n64742-83-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-356-00-4\nSolvent naphtha (petroleum), light arom.;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained from distillation of aromatic streams. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C10 and boiling in the range of approximately 135 °C to 210 °C (275 °F to 410 °F).]\nH P\n265-199-0\n64742-95-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-357-00-X\nAromatic hydrocarbons, C6-10, acid-treated, neutralized;\nLow boiling point naphtha — unspecified\nH P\n268-618-5\n68131-49-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-358-00-5\nDistillates (petroleum), C3-5, 2-methyl-2-butene-rich;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons from the distillation of hydrocarbons usually ranging in carbon numbers from C3 through C5, predominantly isopentane and 3-methyl-1-butene. It consists of saturated and unsaturated hydrocarbons having carbon numbers in the range of C3 through C5, predominantly 2-methyl-2-butene.]\nH P\n270-725-7\n68477-34-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-359-00-0\nDistillates (petroleum), polymd. steam-cracked petroleum distillates, C5-12 fraction;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained from the distillation of polymerized steam-cracked petroleum distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C12.]\nH P\n270-735-1\n68477-50-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-360-00-6\nDistillates (petroleum), steam-cracked, C5-12 fraction;\nLow boiling point naphtha — unspecified;\n[A complex combination of organic compounds obtained by the distillation of products from a steam cracking process. It consists of unsaturated hydrocarbons having carbon numbers predominantly in the range of C5 through C12.]\nH P\n270-736-7\n68477-53-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-361-00-1\nDistillates (petroleum), steam-cracked, C5-10 fraction, mixed with light steam-cracked petroleum naphtha C5 fraction;\nLow boiling point naphtha — unspecified\nH P\n270-738-8\n68477-55-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-362-00-7\nExtracts (petroleum), cold-acid, C4-6;\nLow boiling point naphtha — unspecified;\n[A complex combination of organic compounds produced by cold acid unit extraction of saturated and unsaturated aliphatic hydrocarbons usually ranging in carbon numbers from C3 through C6, predominantly pentanes and amylenes. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers in the range of C4 through C6, predominantly C5.]\nH P\n270-741-4\n68477-61-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-363-00-2\nDistillates (petroleum), depentanizer overheads;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained from a catalytic cracked gas stream. It consists of aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C6.]\nH P\n270-771-8\n68477-89-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-364-00-8\nResidues (petroleum), butane splitter bottoms;\nLow boiling point naphtha — unspecified;\n[A complex residuum from the distillation of butane stream. It consists of aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C6.]\nH P\n270-791-7\n68478-12-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C <10 %: T; R45-46\n4\n649-365-00-3\nResidual oils (petroleum), deisobutanizer tower;\nLow boiling point naphtha — unspecified;\n[A complex residuum from the atmospheric distillation of the butane-butylene stream. It consists of aliphatic hydrocarbons having carbon numbers predominantly in the range of C4 through C6.]\nH P\n270-795-9\n68478-16-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-366-00-9\nNaphtha (petroleum), full-range coker;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons produced by the distillation of products from a fluid coker. It consists predominantly of unsaturated hydrocarbons having carbon numbers predominantly in the range of C4 through C15 and boiling in the range of approximately 43 °C to 250 °C (110 °F-500 °F).]\nH P\n270-991-4\n68513-02-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-367-00-4\nNaphtha (petroleum), steam-cracked middle arom.;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons produced by the distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 130 °C to 220 °C (266 °F to 428 °F).]\nH P\n271-138-9\n68516-20-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-368-00-X\nNaphtha (petroleum), clay-treated full-range straight-run;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons resulting from treatment of full-range straight-run naphtha with natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately -20 °C to 220 °C (-4 °F to 429 °F).]\nH P\n271-262-3\n68527-21-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-369-00-5\nNaphtha (petroleum), clay-treated light straight-run;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons resulting from treatment of light straight-run naphtha with a natural or modified clay, usually in a percolation process to remove the trace amounts of polar compounds and impurities present. It consists of hydrocarbons having carbon numbers predominantly in the range of C7 through C10 and boiling in the range of approximately 93 °C to 180 °C (200 °F to 356 °F).]\nH P\n271-263-9\n68527-22-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-370-00-0\nNaphtha (petroleum), light steam-cracked arom.;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C9 and boiling in the range of approximately 110 °C to 165 °C (230 °F to 329 °F).]\nH P\n271-264-4\n68527-23-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-371-00-6\nNaphtha (petroleum), light steam-cracked, debenzenized;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons produced by distillation of products from a steam-cracking process.t consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C12 and boiling in the range of approximately 80 °C to 218 °C (176 °F to 424 °F).]\nH P\n271-266-5\n68527-26-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-372-00-1\nNaphtha (petroleum), arom.-contg.;\nLow boiling point naphtha — unspecified\nH P\n271-635-0\n68603-08-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-373-00-7\nGasoline, pyrolysis, debutanizer bottoms;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained from the fractionation of depropanizer bottoms. It consists of hydrocarbons having carbon numbers predominantly greater than C5.]\nH P\n271-726-5\n68606-10-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-374-00-2\nNaphtha (petroleum), light, sweetened;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by subjecting a petroleum distillate to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of saturated and unsaturated hydrocarbons having carbon numbers predominantly in the range of C3 through C6 and boiling in the range of approximately -20 °C to 100 °C (-4 °F to 212 °F).]\nH P\n272-206-0\n68783-66-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-375-00-8\nNatural gas condensates;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons separated and/or condensed from natural gas during transportation and collected at the wellhead and/or from the production, gathering, transmission, and distribution pipelines in deeps, scrubbers, etc. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C2 through C8.]\nH J\n272-896-3\n68919-39-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-376-00-3\nDistillates (petroleum), naphtha unifiner stripper;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons produced by stripping the products from the naphtha unifiner. It consists of saturated aliphatic hydrocarbons having carbon numbers predominantly in the range of C2 through C6.]\nH P\n272-932-8\n68921-09-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-377-00-9\nNaphtha (petroleum), catalytic reformed light, arom.-free fraction;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons remaining after removal of aromatic compounds from catalytic reformed light naphtha in a selective absorption process. It consists predominantly of paraffinic and cyclic compounds having carbon numbers predominantly in the range of C5 to C8 and boiling in the range of approximately 66 °C to 121 °C (151 °F to 250 °F).]\nH P\n285-510-3\n85116-59-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-378-00-4\nGasoline;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons consisting primarily of paraffins, cycloparaffins, aromatic and olefinic hydrocarbons having carbon numbers predominantly greater than C3 and boiling in the range of 30 °C to 260 °C (86 °F to 500 °F).]\nH P\n289-220-8\n86290-81-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-379-00-X\nAromatic hydrocarbons, C7-8, dealkylation products, distn. residues;\nLow boiling point naphtha — unspecified\nH P\n292-698-0\n90989-42-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-380-00-5\nHydrocarbons, C4-6, depentanizer lights, arom. hydrotreater;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained as first runnings from the depentanizer column before hydrotreatment of the aromatic charges. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C6, predominantly pentanes and pentenes, and boiling in the range of approximately 25 °C to 40 °C (77 °F to 104 °F).]\nH P\n295-298-4\n91995-38-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-381-00-0\nDistillates (petroleum), heat-soaked steam-cracked naphtha, C5-rich;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by distillation of heat-soaked steam-cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C4 through C6, predominantly C5.]\nH P\n295-302-4\n91995-41-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-382-00-6\nExtracts (petroleum), catalytic reformed light naphtha solvent;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained as the extract from the solvent extraction of a catalytically reformed petroleum cut. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C7 through C8 and boiling in the range of approximately 100 °C to 200 °C (212 °F to 392 °F).]\nH P\n295-331-2\n91995-68-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-383-00-1\nNaphtha (petroleum), hydrodesulfurized light, dearomatized;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by distillation of hydrodesulfurized and dearomatized light petroleum fractions. It consists predominantly of C7 paraffins and cycloparaffins boiling in a range of approximately 90 °C to 100 °C (194 °F to 212 °F).]\nH P\n295-434-2\n92045-53-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-384-00-7\nNaphtha (petroleum), light, C5-rich, sweetened;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists of hydrocarbons having carbon numbers predominantly in the range of C4 through C5, predominantly C5, and boiling in the range of approximately minus 10 °C to 35 °C (14 °F to 95 °F).]\nH P\n295-442-6\n92045-60-8\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-385-00-2\nHydrocarbons, C8-11, naphtha-cracking, toluene cut;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by distillation from prehydrogenated cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C8 through C11 and boiling in the range of approximately 130 °C to 205 °C (266 °F to 401 °F).]\nH P\n295-444-7\n92045-62-0\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-386-00-8\nHydrocarbons, C4-11, naphtha-cracking, arom.-free;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained from prehydrogenated cracked naphtha after distillative separation of benzene- and toluene-containing hydrocarbon cuts and a higher boiling fraction. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C4 through C11 and boiling in the range of approximately 30 °C to 205 °C (86 °F to 401 °F).]\nH P\n295-445-2\n92045-63-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-387-00-3\nNaphtha (petroleum), light heat-soaked, steam-cracked;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by the fractionation of steam cracked naphtha after recovery from a heat soaking process. It consists predominantly of hydrocarbons having a carbon number predominantly in the range of C4 through C6 and boiling in the range of approximately 0 °C to 80 °C (32 °F to 176 °F).]\nH P\n296-028-8\n92201-97-3\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-388-00-9\nDistillates (petroleum), C6-rich;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained from the distillation of a petroleum feedstock. It consists predominantly of hydrocarbons having carbon numbers of C5 through C7, rich in C6, and boiling in the range of approximately 60 °C to 70 °C (140 °F to 158 °F).]\nH P\n296-903-4\n93165-19-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-389-00-4\nGasoline, pyrolysis, hydrogenated;\nLow boiling point naphtha-unspecified;\n[A distillation fraction from the hydrogenation of pyrolysis gasoline boiling in the range of approximately 20 °C to 200 °C (68 °F to 392 °F).]\nH P\n302-639-3\n94114-03-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-390-00-X\nDistillates (petroleum), steam-cracked, C8-12 fraction, polymd., distn. lights;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by distillation of the polymerized C8 through C12 fraction from steam-cracked petroleum distillates. It consists predominantly of aromatic hydrocarbons having carbon numbers predominantly in the range of C8 through C12.]\nH P\n305-750-5\n95009-23-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-391-00-5\nExtracts (petroleum) heavy naphtha solvent, clay-treated;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by the treatment of heavy naphthic solvent petroleum extract with bleaching earth. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C10 and boiling in the range of approximately 80 °C to 180 °C (175 °F to 356 °F).]\nH P\n308-261-5\n97926-43-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-392-00-0\nNaphtha (petroleum), light steam-cracked, debenzenized, thermally treated;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by the treatment and distillation of debenzenized light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C7 through C12 and boiling in the range of approximately 95 °C to 200 °C (203 °F to 392 °F).]\nH P\n308-713-1\n98219-46-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-393-00-6\nNaphtha (petroleum), light steam-cracked, thermally treated;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by the treatment and distillation of light steam-cracked petroleum naphtha. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C6 and boiling in the range of approximately 35 °C to 80 °C (95 °F to 176 °F).]\nH P\n308-714-7\n98219-47-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-394-00-1\nDistillates (petroleum), C7-9, C8-rich, hydrodesulfurized dearomatized;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by the distillation of petroleum light fraction, hydrodesulfurized and dearomatized. It consists predominantly of hydrocarbons having carbon numbers in the range of C7 through C9, predominantly C8 paraffins and cycloparaffins, boiling in the range of approximately 120 °C to 130 °C (248 °F to 266 °F).]\nH P\n309-862-5\n101316-56-7\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-395-00-7\nHydrocarbons, C6-8, hydrogenated sorption-dearomatized, toluene raffination;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained during the sorptions of toluene from a hydrocarbon fraction from cracked gasoline treated with hydrogen in the presence of a catalyst. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C6 through C8 and boiling in the range of approximately 80 °C to 135 °C (176 °F to 275 °F).]\nH P\n309-870-9\n101316-66-9\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-396-00-2\nNaphtha (petroleum), hydrodesulfurised full-range coker;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by fractionation from hydrodesulfurised coker distillate. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 to C11 and boiling in the range of approximately 23 °C to 196 °C (73 °F to 385 °F).]\nH P\n309-879-8\n101316-76-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-397-00-8\nNaphtha (petroleum), sweetened light;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by subjecting a petroleum naphtha to a sweetening process to convert mercaptans or to remove acidic impurities. It consists predominantly of hydrocarbons having carbon numbers predominantly in the range of C5 through C8 and boiling in the range of approximately 20 °C to 130 °C (68 °F to 266 °F).]\nH P\n309-976-5\n101795-01-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-398-00-3\nHydrocarbons, C3-6, C5-rich, steam-cracked naphtha;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by distillation of steam-cracked naphtha. It consists predominantly of hydrocarbons having carbon numbers in the range of C3 through C6, predominantly C5.]\nH P\n310-012-0\n102110-14-5\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-399-00-9\nHydrocarbons, C5-rich, dicyclopentadiene-contg.;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by distillation of the products from a steam-cracking process. It consists predominantly of hydrocarbons having carbon numbers of C5 and dicyclopentadiene and boiling in the range of approximately 30 °C to 170 °C (86 °F to 338 °F).]\nH P\n310-013-6\n102110-15-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-400-00-2\nResidues (petroleum), steam-cracked light, arom.;\nLow boiling point naphtha — unspecified;\n[A complex combination of hydrocarbons obtained by the distillation of the products of steam cracking or similar processes after taking off the very light products resulting in a residue starting with hydrocarbons having carbon numbers greater than C5. It consists predominantly of aromatic hydrocarbons having carbon numbers greater than C5 and boiling above approximately 40 °C (104 °F).]\nH P\n310-057-6\n102110-55-4\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-401-00-8\nHydrocarbons, C≥ 5, C5-6-rich;\nLow boiling point naphtha — unspecified\nH P\n270-690-8\n68476-50-6\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-402-00-3\nHydrocarbons, C5-rich;\nLow boiling point naphtha — unspecified\nH P\n270-695-5\n68476-55-1\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4\n649-403-00-9\nAromatic hydrocarbons, C8-10;\nLow boiling point naphtha — unspecified\nH P\n292-695-4\n90989-39-2\nCarc. Cat. 2; R45\nMuta. Cat. 2; R46\nXn; R65\nT\nR: 45-46-65\nS: 53-45\nC ≥ 10 %: T; R45-46-65\n0,1 % ≤ C < 10 %: T; R45-46\n4’",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eudr/2008/58/annex/1F",
    "retrieved_at": "2026-11-01T15:22:20.633562+00:00"
  },
  "licence": "Open Government Licence v3.0",
  "licence_url": "https://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/",
  "attribution": "Contains public sector information licensed under the Open Government Licence v3.0. Source: legislation.gov.uk, The National Archives."
}