{
  "url": "https://openlegislation.uk/eu-directive-2011-6/annex",
  "json_url": "https://openlegislation.uk/eu-directive-2011-6/annex.json",
  "legislation": "eudr/2011/6",
  "legislation_title": "Commission Directive 2011/6/EU of 20 January 2011 amending Council Directive 91/414/EEC to include buprofezin as active substance (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-directive-2011-6",
  "path": "annex",
  "kind": "annex",
  "number": null,
  "heading": null,
  "text": "The following entry shall be added at the end of the table in Annex I to Directive 91/414/EEC:\nFurther details on identity and specification of active substance are provided in the review report.\nNo\nCommon Name, Identification Numbers\nIUPAC Name\nPurity\nEntry into force\nExpiration of inclusion\nSpecific provisions\n‘325\nBuprofezin\nCAS No: 953030-84-7\nCIPAC No: 681\n(Z)-2-tert-butylimino-3-isopropyl-5-phenyl-1,3,5-thiadiazinan-4-one\n≥ 985 g/kg\n1 February 2011\n31 January 2021\nPART A\nOnly uses as insecticide and acaricide may be authorised.\nPART B\nFor the implementation of the uniform principles of Annex VI the conclusions of the review report on buprofezin, and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health on 23 November 2010, shall be taken into account.\nIn this overall assessment Member States shall pay particular attention to:\n(a) the operators’ and workers’ safety and ensure that conditions of use impose adequate personal protective equipment where appropriate;\n(b) the dietary exposure of consumers to the buprofezin (aniline) metabolites in processed food;\n(c) the application of an appropriate waiting period for rotational crops in greenhouses;\n(d) the risk to aquatic organisms and ensure that conditions of use impose adequate risk mitigation measures, where appropriate.\nThe Member States concerned shall request the submission of confirmatory information as regards the processing and conversion factors for consumer risk assessment.\nThe Member States concerned shall ensure that the applicant submits such confirmatory information to the Commission by 31 January 2013.’",
  "extent": "E+W+S+N.I.",
  "status": null,
  "version": "current",
  "annotations": [
    {
      "type": "footnote",
      "label": "f1",
      "text": "Further details on identity and specification of active substance are provided in the review report."
    }
  ],
  "outstanding_effects": [],
  "provenance": {
    "source": "legislation.gov.uk",
    "source_url": "https://www.legislation.gov.uk/eudr/2011/6/annex",
    "retrieved_at": "2026-11-01T15:22:03.466998+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."
}