{
  "url": "https://openlegislation.uk/eu-directive-2011-25/annex",
  "json_url": "https://openlegislation.uk/eu-directive-2011-25/annex.json",
  "legislation": "eudr/2011/25",
  "legislation_title": "Commission Directive 2011/25/EU of 3 March 2011 amending Council Directive 91/414/EEC to include bupirimate as active substance and amending Commission Decision 2008/934/EC (Text with EEA relevance)",
  "legislation_url": "https://openlegislation.uk/eu-directive-2011-25",
  "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‘337\nBupirimate\nCAS No: 41483-43-6\nCIPAC No: 261\n5-butyl-2-ethylamino-6-methylpyrimidine-4-yl dimethylsulfamate\n≥ 945 g/kg\nImpurities:\nEthirimol: max. 2 g/kg\nToluene: max. 3 g/kg\n1 June 2011\n31 May 2021\nPART A\nOnly uses as fungicide may be authorised.\nPART B\nFor the implementation of the uniform principles of Annex VI, the conclusions of the review report on bupirimate, and in particular Appendices I and II thereof, as finalised in the Standing Committee on the Food Chain and Animal Health on 28 January 2011 shall be taken into account.\nIn this overall assessment Member States shall pay particular attention to:\nthe protection of aquatic organisms. Conditions of authorisation shall include risk mitigation measures, where appropriate,\nthe protection of the groundwater, when the active substance is applied in regions with vulnerable soil and/or climatic conditions. Conditions of authorisation shall include risk mitigations, where appropriate,\nthe in-field risk to non-target arthropods.\nThe Member States concerned shall request the submission of confirmatory information as regards:\n(1) the specification of the technical material, as commercially manufactured, by appropriate analytical data; including information on the relevance of the impurities;\n(2) the equivalence between the specifications of the technical material; as commercially manufactured, and those of the test material used in the toxicity dossiers;\n(3) the kinetic parameters, the soil degradation and the adsorption and desorption parameter for the major soil metabolite DE-B (de-ethyl-bupirimate).\nThe Member States concerned shall ensure that the applicant submits such confirmatory data and information to the Commission set out in points (1) and (2) by 30 November 2011 and the information set out in point (3) by 31 May 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/2011/25/annex",
    "retrieved_at": "2026-11-01T15:22:02.415043+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."
}