Commission Regulation (EU) No 944/2013 of 2 October 2013 amending, for the purposes of its adaptation to technical and scientific progress, Regulation (EC) No 1272/2008 of the European Parliament and of the Council on classification, labelling and packaging of substances and mixtures (Text with EEA relevance)

magnesium phosphide;

trimagnesium diphosphide

fenamiphos (ISO);

ethyl-4-methylthio-m-tolyl isopropyl phosphoramidate

M = 100

M = 100

chloroform;

trichloromethane

1,1’,1’-nitrilotripropan-2-ol;

triisopropanolamine

GHS07

Wng

acrolein;

prop-2-enal;

acrylaldehyde

reaction mass of:

• succinic acid

• monopersuccinic acid

• dipersuccinic acid

• monomethyl ester of succinic acid

• monomethyl ester of persuccinic acid

• dimethyl succinate glutaric acid

• monoperglutaric acid

• diperglutaric acid

• monomethyl ester of glutaric acid

• monomethyl ester of perglutaric acid

• dimethyl glutarate adipic acid

• monoperadipic acid

• diperadipic acid

• monomethyl ester of adipic acid

• monomethyl ester of peradipic acid

• dimethyl adipate

• hydrogen peroxide

• methanol

• water

aclonifen (ISO);

2-chloro-6-nitro-3-phenoxyaniline

M = 100

M = 10

epoxiconazole (ISO);

(2RS,3SR)-3-(2-chlorophenyl)-2-(4-fluorophenyl)-[( 1H-1,2,4-triazol-1-yl)methyl]oxirane

pitch, coal tar, high-temp.;

[The residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 30 °C to 180 °C (86 °F to 356 °F). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.]

M = 1000

M = 1000

naphtha (petroleum), hydrodesulphurized heavy;

Low boiling point hydrogen treated naphtha;

[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).]

stoddard solvent;

Low boiling point naphtha — unspecified;

[A colourless, refined petroleum distillate that is free from rancid or objectionable odours and that boils in a range of approximately 148,8 °C to 204,4 °C (300 °F to 400 °F).]

solvent naphtha (petroleum), medium aliph.;

Straight run kerosine;

[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 C9 through C12 and boiling in the range of approximately 140 °C to 220 °C (284 °F to 428 °F).]

GHS08

Wng

GHS08

Wng

GHS08

Dgr

GHS08

Dgr

sulcotrione (ISO);

2-[2-chloro-4-(methylsulfonyl)benzoyl]cyclohexane-1,3-dione

M = 1

M = 10

bifenthrin (ISO);

(2-methylbiphenyl-3-yl)methyl rel-(1R,3R)-3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate

M = 10 000

M = 100 000

indoxacarb (ISO);

methyl (4aS)-7-chloro-2-{(methoxycarbonyl)[4-(trifluoromethoxy)phenyl]carbamoyl}-2,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylate [1]

M = 1

M = 1

reaction mass of (S)- Indoxacarb and (R)- Indoxacarb 75:25;

methyl 7-chloro-2-{(methoxycarbonyl)[4-(trifluoromethoxy)phenyl]carbamoyl}-2,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylate [2]

GHS08

Dgr

M = 10

M = 10

M = 10

M = 10

M = 10

M = 10

M = 10

M = 10

M = 10

M = 10

flufenoxuron (ISO);

1-(4-(2-cloro-α,α,α-p-trifluorotolyloxy)-2-fluorophenyl)-3-(2,6-difluorobenzolyl)urea

M = 10 000

M = 10 000

M = 10

M = 10

N-ethyl-2-pyrrolidone;

1-ethylpyrrolidin-2-one

GHS08

Dgr

amidosulfuron (ISO);

3-(4,6-dimethoxypyrimidin-2-yl)-1-((N-methyl-N-methylsulfonylamino)sulfonyl)urea

M = 100

M = 100

tebufenpyrad (ISO);

N-(4-tertbutylbenzyl)-4-chloro-3-ethyl-1-methyl-1Hpyrazole-5- carboxamide

M = 10

M = 10

proquinazid (ISO);

6-iodo-2-propoxy-3-propylquinazolin-4(3H)-one

M = 1

M = 10

F; R15/29

T+; R26/28

Xn; R21

R32

N; R50

F; T+; N

R: 15/29-21-26/28-32-50

S: (1/2-)3/9/14/49-8-22-30-36/37-43-45-60-61

magnesium phosphide;

trimagnesium diphosphide

F; R15/29

T+; R26/28

Xn; R21

R32

N; R50

F; T+; N

R: 15/29-21-26/28-32-50

S: (1/2-)3/9/14/49-8-22-30-36/37-43-45-60-61

fenamiphos (ISO);

ethyl-4-methylthio-m-tolyl isopropyl phosphoramidate

T+; R26/28

T; R24

Xi; R36

N; R50-53

T+; N

R: 24-26/28-36-50/53

S: (1/2-)23-26-28-35-36/37-45-60-61

N; R50-53: C ≥ 0,25 %

N; R51-53: 0,025 % ≤ C < 0,25 %

R52-53: 0,0025 % ≤ C < 0,025 %

R: 53

S: 61

chloroform;

trichloromethane

Carc. Cat. 3; R40

Repr. Cat. 3; R63

Xn; R20/22-48/20

Xi; R36/38

Xn

R: 20/22-36/38-40-48/20-63

S: (2-)36/37

1,1′,1′′-nitrilotripropan-2-ol;

triisopropanolamine

Xi

R: 36

S: (2-)26

acrolein;

prop-2-enal;

acrylaldehyde

F; R11

T+; R26/28

T; R24

C; R34

N; R50

F; T+; N

R: 11-24-26/28-34-50

S: (1/2-)23-26-28-36/37/39-45-61

C; R34: C ≥ 0,1 %

N; R50: C ≥ 0,25 %

F; R11

Carc. Cat. 3; R40

Xn; R20

Xi; R37

F; Xn

R: 11-20-37-40

S: 9-16-33-36/37

reaction mass of:

• succinic acid

• monopersuccinic acid

• dipersuccinic acid

• monomethyl ester of succinic acid

• monomethyl ester of persuccinic acid

• dimethyl succinate

• glutaric acid

• monoperglutaric acid

• diperglutaric acid

• monomethyl ester of glutaric acid

• monomethyl ester of perglutaric acid

• dimethyl glutarate

• adipic acid

• monoperadipic acid

• diperadipic acid

• monomethyl ester of adipic acid

• monomethyl ester of peradipic acid

• dimethyl adipate

• hydrogen peroxide

• methanol

• water

C; R34

Xn; R20/21/22-68/20/21/22

C

R: 20/21/22-34-68/20/21/22

S: (1/2-)26-28-36/37/39-45

Carc. Cat. 3; R40

Repr. Cat. 2; R60

T; R23/24/25-48/23/24/25

R52-53

T

R: 23/24/25-48/23/24/25-40-60-52/53

S: 45-53

aclonifen (ISO);

2-chloro-6-nitro-3-phenoxyaniline

Carc. Cat. 3; R40

R43

N; R50-53

Xn; N

R: 40-43-50/53

S: (2-)36/37-60-61

R43: C ≥ 0,1 %

N; R50-53: C ≥ 0,25 %

N; R51-53: 0,025 % ≤ C < 0,25 %

R52-53: 0,0025 % ≤ C < 0,025 %

epoxiconazole (ISO);

(2RS,3SR)-3-(2-chlorophenyl)-2-(4-fluorophenyl)-[(1H-1,2,4-triazol-1-yl)methyl]oxirane

Carc. Cat. 3; R40

Repr. Cat. 2; R61

Repr. Cat. 3; R62

N; R51-53

T; N

R: 61-40-62-51/53

S: 45-53-61

R: 53

S: 61

pitch, coal tar, high-temp.;

[The residue from the distillation of high temperature coal tar. A black solid with an approximate softening point from 30 °C to 180 °C (86 °F to 356 °F). Composed primarily of a complex mixture of three or more membered condensed ring aromatic hydrocarbons.]

Carc. Cat. 1; R45

Muta. Cat. 2; R46

Repr. Cat. 2; R60-61

N; R50-53

T; N

R: 45-46-60-61-50/53

S: 45-53-60-61

N; R50-53: C ≥ 0,025 %

N; R51-53: 0,0025 % ≤ C <

0,025 %

R52-53: 0,00025 % ≤ C <

0,0025 %

naphtha (petroleum), hydrodesulphurized heavy;

Low boiling point hydrogen treated naphtha;

[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).]

Carc. Cat. 2; R45

Muta. Cat. 2; R46

Xn; R48/20-65

T

R: 45-46-48/20-65

S: 45-53

stoddard solvent;

Low boiling point naphtha — unspecified;

[A colourless, refined petroleum distillate that is free from rancid or objectionable odours and that boils in a range of approximately 148,8 °C to 204,4 °C (300 °F to 400 °F).]

Carc. Cat. 2; R45

Muta. Cat. 2; R46

Xn; R48/20-65

T

R: 45-46-48/20-65

S: 45-53

solvent naphtha (petroleum), medium aliph.;

Straight run kerosine;

[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 C9 through C12 and boiling in the range of approximately 140 °C to 220 °C (284 °F to 428 °F).]

Xn

R: 48/20-65

S: (2-)23-24-62

Carc. Cat. 2; R45

T; R48/23

T

R: 45-48/23

S: 45-53

Xn

R: 63

S: (2-)22-36/37

Xn

R: 63

S: (2-)22-36/37

T

R: 61

S: 45-53

F; R11

Xn; R65

R67

F; Xn

R: 11-65-67

S: 9-16-33-62

sulcotrione (ISO);

2-[2-chloro-4-(methylsulfonyl)benzoyl]cyclohexane-1,3-dione

Repr. Cat. 3; R63

Xn; R48/22

R43

N; R50-53

Xn; N

R: 43-48/22-63-50/53

S: (2-)22-36/37-60-61

N; R50-53: C ≥ 25 %

N; R51-53: 2,5 % ≤ C < 25 %

R52-53: 0,25 % ≤ C< 2,5 %

R43: C ≥ 0,1 %

bifenthrin (ISO);

(2-methylbiphenyl-3-yl)methyl rel-(1R,3R)-3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylate

Carc. Cat 3; R40

T; R23/25

Xn; R48/22

R43

N; R50-53

T; N

R: 23/25-40-43-48/22-50/53

S: (1/2-)23-24-36/37-38- 45-60-61

N; R50-53: C ≥ 0,0025 %

N; R51-53: 0,00025 % ≤ C< 0,0025 %

R52-53: 0,000025 % ≤ C < 0,00025 %

indoxacarb (ISO);

methyl (4aS)-7-chloro-2-{(methoxycarbonyl)[4-(trifluoromethoxy)phenyl]carbamoyl}-2,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylate

T; R25-48/25

Xn; R20

R43

N; R50-53

T; N

R: 20-25-43-48/25-50/53

S: (1/2-)24-37-45-60-61

N; R50-53: C ≥ 25 %

N; R51-53: 2,5 % ≤ C < 25 %

R52-53: 0,25 % ≤ C < 2,5 %

reaction mass of (S)- Indoxacarb and (R)- Indoxacarb 75:25;

methyl 7-chloro-2-{(methoxycarbonyl)[4-(trifluoromethoxy)phenyl]carbamoyl}-2,5-dihydroindeno[1,2-e][1,3,4]oxadiazine-4a(3H)-carboxylate

T; R48/25

Xn; R20/22

R43

N; R50-53

T; N

R: 20/22-43-48/25-50/53

S: (1/2-)24-37-45-60-61

N; R50-53: C ≥ 25 %

N; R51-53: 2,5 % ≤ C < 25 %

R52-53: 0,25 % ≤ C < 2,5 %

T

R: 60-61

S: 45-53

Carc. Cat. 3; R40

Repr. Cat. 2; R61

R64

T; R48/23

Xn; R20/22-48/21/22

Xi; R41

T

R: 61-20/22-40-41- 48/23-48/21/22-64

S: 45-53

Carc. Cat. 3; R40

Repr. Cat. 2; R61

R64

T; R48/23

Xn; R20/22-48/21/22

Xi; R41

T

R: 61-20/22-40-41-48/23-48/21/22-64

S: 45-53

Xn; R48/22-65

Xi; R38-41

N; R50-53

Xn; N

R: 38-41-48/22-65-50/53

S: (2-)26-36/37/39-60-61-62

N; R50-53: C ≥ 2,5 %

N; R51-53: 0,25 % ≤ C < 2,5 %

R52-53: 0,025 % ≤ C < 0,25 %

Xn; R22-48/22-65

C; R34

N; R50-53

C; N

R: 22-34-48/22-65-50/53

S: (1/2-)23-26-36/37/39-45-60-61-62

C; R34: C ≥ 10 %

Xi; R36/37/38: 5 % ≤ C < 10 %

N; R50-53: C ≥ 2,5 %

N; R51-53: 0,25 % ≤ C < 2,5 %

R52-53: 0,025 % ≤ C < 0,25 %

Xn; R48/22-65

Xi; R38-41

N; R50-53

Xn; N

R: 38-41-48/22-65-50/53

S: (2-)26-36/37/39-60-61-62

N; R50-53: C ≥ 2,5 %

N; R51-53: 0,25 % ≤ C < 2,5 %

R52-53: 0,025 % ≤ C < 0,25 %

Xn; R22-48/22-65

C; R35

N; R50-53

C; N

R: 22-35-48/22-65-50/53

S: (1/2-)23-26-36/37/39-45-60-61-62

C; R35: C ≥ 10 %

C; R34: 5 % ≤ C < 10 %

Xi; R36/37/38: 1 % ≤ C < 5 %

N; R50-53: C ≥ 2,5 %

N; R51-53: 0,25 % ≤ C < 2,5 %

R52-53: 0,025 % ≤ C < 0,25 %

Xn; R22-48/22-65

C; R35

N; 50-53

C; N

R: 22-35-48/22-65-50/53

S: (1/2-)26-36/37/39-45-60-61-62

N; R50-53: C ≥ 2,5 %

N; R51-53: 0,25 % ≤ C < 2,5 %

R52-53: 0,025 % ≤ C < 0,25 %

flufenoxuron (ISO);

1-(4-(2-cloro-α,α,α-p-trifluorotolyloxy)-2-fluorophenyl)-3-(2,6-difluorobenzolyl)urea

R64

R33

N; R50-53

N

R: 33-64-50/53

S: (2-)22-36/37-46-60-61

N; R50-53 C ≥ 0,0025 %

N; R51-53 0,00025 % ≤ C < 0,0025 %

R52-53 0,000025 % ≤ C < 0,00025 %

Carc. Cat 3; R40

Xn; R22

T; R48/23

Xi; R41

R43

N; R50-53

T; N

R: 22-40-41-43-48/23-50/53

S: (1/2-)22-36/37/39-45-60-61

N; R50-53: C ≥ 2,5 %

N; R51-53: 0,25 % ≤ C < 2,5 %

R52-53: 0,025 % ≤ C < 0,25 %

N-ethyl-2-pyrrolidone;

1-ethylpyrrolidin-2-one

T

R: 61

S: 45-53

amidosulfuron (ISO);

3-(4,6-dimethoxypyrimidin-2-yl)-1-((N-methyl-N-methylsulfonylamino)sulfonyl)urea

N

R: 50/53

S: 60-61

N; R50-53: C ≥ 0,25 %

N; R51-53: 0,025 % ≤ C < 0,25 %

R52-53: 0,0025 % ≤ C < 0,025 %

tebufenpyrad (ISO);

N-(4-tertbutylbenzyl)-4-chloro-3-ethyl-1-methyl-1Hpyrazole-5-carboxamide

Xn; R20/22

R43

N; R50-53

Xn; N

R: 20/22-43-50/53

S: (2-)24-37-46-60-61

N; R50-53: C ≥ 2,5 %

N; R51-53: 0,25 % ≤ C < 2,5 %

R52-53: 0,025 % ≤ C < 0,25 %

proquinazid (ISO);

6-iodo-2-propoxy-3-propylquinazolin-4(3H)-one

Carc. Cat. 3; R40

N; R50-53

Xn; N

R: 40-50/53

S: (2-)36/37-46-60-61