Flocoumafen

CAS90035-08-8
EC421-960-0

List details

Active substance data

Substance information page external link [echa.europa.eu]
Product type PT14-Rodenticides
BAS number 34
Candidate for substitution Yes
Regulatory Process
  • Review programme substance
Approval status Approved

Approval data

Evaluating competent authority
  • Netherlands
R4BP asset number EU-0005378-0000
Validity of approval - start date 2011-10-01
Validity of approval - end date 2024-06-30

Other data

Related authorised biocidal products 7
Factsheet URL external link [echa.europa.eu]
RML Id 100.102.053
Inclusion category 0

Related substances

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Related regulatory records

  • Registered substances under the name A mixture of: cis-4-hydroxy-3-(1,2,3,4-tetrahydro-3-(4-(4-trifluoromethylbenzyloxy)phenyl)-1-naphthyl)coumarin; trans-4-hydroxy-3-(1,2,3,4-tetrahydro-3-(4-(4-trifluoromethylbenzyloxy)phenyl)-1-naphthyl)coumarin
    Tonnage band: Tonnage Data Confidential
  • Registry of CLH intentions until outcome under the name A mixture of: cis-4-hydroxy-3-(1,2,3,4-tetrahydro-3-(4-(4-trifluoromethylbenzyloxy)phenyl)-1-naphthyl)coumarin; trans-4-hydroxy-3-(1,2,3,4-tetrahydro-3-(4-(4-trifluoromethylbenzyloxy)phenyl)-1-naphthyl)coumarin
    Deadline for commenting: 2013-04-19
  • Harmonised classification and labelling (CLP Annex VI) under the name flocoumafen (ISO); reaction mass of: cis-4-hydroxy-3-(1,2,3,4-tetrahydro-3-(4-(4-trifluoromethylbenzyloxy)phenyl)-1-naphthyl)coumarin and trans-4-hydroxy-3-(1,2,3,4-tetrahydro-3-(4-(4-trifluoromethylbenzyloxy)phenyl)-1-naphthyl)coumarin
    Hazard Class and Category Codes: Repr. 1B: Reproductive toxicity; Acute Tox. 1: Acute toxicity; Acute Tox. 1: Acute toxicity; Acute Tox. 1: Acute toxicity; STOT RE 1: Specific target organ toxicity — repeated exposure; Aquatic Acute 1: Hazardous to the aquatic environment; Aquatic Chronic 1: Hazardous to the aquatic environment

Record history

The following timeline shows when we detected changes of this regulatory record (the date might slightly differ from the date of the actual change). Additions between versions are hightlighted in green color, red color shows data removed between versions.

This version
July 9, 2019
  • Validity of approval - end date: 2024-06-30
  • Validity of approval - start date: 2011-10-01
  • Approval status: Approved
  • Evaluating competent authority: Netherlands
  • Legal act: Reg (EU) 2017/1383
  • Legal act URL: http://eur-lex.europa.eu/legal-content/EN/ALL/?uri=CELEX:32017R1383
  • R4BP asset number: EU-0005378-0000
June 25, 2019
  • Validity of approval - end date: 2024-06-30
  • Validity of approval - start date: 2011-10-01
  • Approval status: Approved
  • Evaluating competent authority: Netherlands
  • R4BP asset number: EU-0005378-0000
June 5, 2019
  • Candidate for substitution: Under AssessmentYes
Feb. 4, 2019
  • Annex I Substance Flag: false
  • Validity of approval - end date: 2024-06-30
  • Validity of approval - start date: 2011-10-01
  • Date of approval: 2011-10-01
  • Evaluating competent authority: NLNetherlands
  • Expiry date: 2024-07-01
  • BAS number: 34
  • Candidate for substitution: Under Assessment
  • Factsheet URL: https://echa.europa.eu/information-on-chemicals/biocidal-active-substances/-/disas/factsheet/34/PT14
  • Inclusion category: 0
  • Type: 14 - Rodenticides
  • Legal act URL: http://eur-lex.europa.eu/legal-content/EN/ALL/?uri=CELEX:32017R1383
  • New Active Substance Flag: false
  • Product type: PT14-Rodenticides
  • R4BP asset number: EU-0005378-0000
  • Related authorised biocidal products: 7
  • Review Programme Flag: true
  • RML Id: 100.102.053
  • Substance information page: https://echa.europa.eu/substance-information/-/substanceinfo/100.102.053
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