{
  "url": "https://openlegislation.uk/eu-regulation-2020-1771/annex",
  "json_url": "https://openlegislation.uk/eu-regulation-2020-1771/annex.json",
  "legislation": "eur/2020/1771",
  "legislation_title": "Commission Implementing Regulation (EU) 2020/1771 of 26 November 2020 approving reaction mass of peracetic acid (PAA) and peroxyoctanoic acid (POOA) as an existing active substance for use in biocidal products of product-types 2, 3 and 4 (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-regulation-2020-1771",
  "path": "annex",
  "kind": "annex",
  "number": null,
  "heading": null,
  "text": "The purity indicated in this column was the minimum degree of purity of the active substance evaluated. The active substance in the product placed on the market can be of equal or different purity if it has been proven to be technically equivalent to the evaluated active substance.\nRegulation (EC) No 1935/2004 of the European Parliament and of the Council of 27 October 2004 on materials and articles intended to come into contact with food and repealing Directives 80/590/EEC and 89/109/EEC (OJ L 338, 13.11.2004, p. 4).\nCommon Name\nIUPAC NameIdentification Numbers\nMinimum degree of purity of the active substance\nDate of approval\nExpiry date of approval\nProduct type\nSpecific conditions\nReaction mass of peracetic acid (PAA) and peroxyoctanoic acid (POOA)\nIUPAC name: Reaction mass of peracetic acid (PAA) and peroxyoctanoic acid (POOA)\nEC No: 201-186-8 and 450-280-7\nCAS No: 79-21-0 and 33734-57-5\nThe minimum purity of the active substance is not relevant as the active substance is a double equilibrium using hydrogen peroxide, acetic acid and octanoic acid as starting materials. The specifications correspond to a range of concentration.\n1 April 2022\n31 March 2032\n2\nThe authorisations of biocidal products are subject to the following conditions:\n(a) The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any uses covered by an application for authorisation, but not addressed in the Union level assessment of the active substance.\n(b) In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to professional users.\nComponents\nSpecifications range content (%w/w)\nActive substance\nPeracetic acid\n1,8–13,9\nActive substance\nPeroxyoctanoic acid\n0,15–2,42\nRelevant impurity\nHydrogn peroxyde\n1,1–25,45\nRelevant impurity\nAcetic acid\n5,74–51\n3\nThe authorisations of biocidal products are subject to the following conditions:\n(a) The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any uses covered by an application for authorisation, but not addressed in the Union level assessment of the active substance.\n(b) In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to professional users.\nRelevant impurity\nOctanoic acid\n1,63–9,03\n4\nThe authorisations of biocidal products are subject to the following conditions:\n(a) The product assessment shall pay particular attention to the exposures, the risks and the efficacy linked to any uses covered by an application for authorisation, but not addressed in the Union level assessment of the active substance.\n(b) Products containing reaction mass of peracetic acid and peroxyoctanoic acid shall not be incorporated in materials and articles intended to come into contact with food within the meaning of Article 1(1) of Regulation (EC) No 1935/2004 of the European Parliament and of the Council, unless the Commission has established specific limits on the migration of reaction mass of peracetic acid and peroxyoctanoic acid into food or it has established] in accordance with that Regulation that such limits are not necessary.\n(c) In view of the risks identified for the uses assessed, the product assessment shall pay particular attention to professional users.",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "footnote",
      "label": "f1",
      "text": "The purity indicated in this column was the minimum degree of purity of the active substance evaluated. The active substance in the product placed on the market can be of equal or different purity if it has been proven to be technically equivalent to the evaluated active substance."
    },
    {
      "type": "footnote",
      "label": "f2",
      "text": "Regulation (EC) No 1935/2004 of the European Parliament and of the Council of 27 October 2004 on materials and articles intended to come into contact with food and repealing Directives 80/590/EEC and 89/109/EEC (OJ L 338, 13.11.2004, p. 4)."
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eur/2020/1771/annex",
    "retrieved_at": "2026-11-01T14:42:20.088437+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."
}