Article 1
Open ↗The approval of the active substance cis-tricos-9-ene for use in biocidal products of product-type 19 is renewed, subject to the conditions set out in the Annex.
Source
Commission Implementing Regulation (EU) 2026/2247 of 12 October 2026 renewing the approval of the active substance cis-tricos-9-ene for use in biocidal products of product-type 19 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council
Commission Implementing Regulation (EU) 2026/2247 of 12 October 2026 renewing the approval of the active substance cis-tricos-9-ene for use in biocidal products of product-type 19 in accordance with Regulation (EU) No 528/2012 of the European Parliament and of the Council
In force
Version historyWe hold this version only; in force from 2026-10-12.
Data as of 2026-11-02 · Compiled from an official source version. Later amendments or repeals may not be reflected; the official text prevails. · Read the official text ↗
Article 2
Open ↗This Regulation shall enter into force on the twentieth day following that of its publication in the Official Journal of the European Union .
Supplementary provisions
ANNEXSupplementary provisions
Open ↗ANNEX Common Name IUPAC Name Identification Numbers Minimum degree of purity of the active substance ( 1 ) Expiry date of approval Product type Specific conditions Muscalure cis-tricos-9-ene EC No: 248-505-7 CAS No: 27519-02-4 80,1 % weight/weight 30 June 2041 19 When assessing the product in the context of the authorisation procedure of biocidal products containing cis-tricos-9-ene as an active substance, the Member States’ competent authorities or, in the case of a Union authorisation the Commission, shall pay particular attention to the exposures, the risks and the efficacy linked to any uses covered by an application for authorisation, but which were not addressed in the Union level assessment of the active substance. ( 1 ) The purity indicated in this column was the minimum degree of purity of the active substance evaluated. The active substance in the product made available on the market may be of equal or different purity if it has been proven to be technically equivalent to the evaluated active substance.
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Source: EUR-Lex (Publications Office of the EU), © European Union, reuse permitted under Commission Decision 2011/833/EU.
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