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Active substance factsheet - Last updated: 28/06/2024

Active substance

Substance 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

EC number:

421-960-0

CAS number:

90035-08-8

IUPAC name:

4-hydroxy-3-[3-(4-{[4-(trifluoromethyl)phenyl]methoxy}phenyl)-1,2,3,4-tetrahydronaphthalen-1-yl]-2H-chromen-2-one

BAS number:

34

Product-type:

PT14

Candidate for substitution:

Yes

Regulatory categorisation:

Review programme substance

Approval/Assessment status:

Approved - Renewal in progress
Competent authority evaluation

Harmonised classification and labeling of the substance

C&L inventory

Related authorised biocidal products

No related authorised products are available

Approval data details
Administrative identifiers

Evaluating competent authority:

Netherlands

R4BP asset number:

EU-0005378-0000

Approval identifiers

Legal act:

Commission Implementing Decision (EU) 2024/734

Validity of approval

Start date:

01/10/2011

End date:

31/12/2026

Documents
Assessment Reports

Assessment Report

AS-RNL_Flocoumafen_PT14_Final Assessment Report.pdf (en)

0034-14_Assessment_Report.pdf (en)

Flocoumafen_PT14_relevant_renewal_data.pdf (en)

Study summaries (Document III-A)

Study summary

Data_003.pdf (en)

Data_006.pdf (en)

Data_004.pdf (en)

Data_001.pdf (en)

Data_011.pdf (en)

Data_007.pdf (en)

Data_008.pdf (en)

Data_010.pdf (en)

Data_002.pdf (en)

Data_005.pdf (en)

Data_012.pdf (en)

Data_009.pdf (en)

Other documents

BPC opinions

Flocoumafen_PT14_Final BPC opinion.pdf (en)

Renewal of active substance
Assessment information

Evaluating competent authority:

Netherlands

Assessment outcome:

In progress

Conclusion date:

Validity of approval

Start date:

End date:

Legal act:

Documents
Assessment Reports
Study summaries (Document III-A)
Other documents
Amendment of active substance - Conclusion Date: 30/04/2024   This item is not a consequence of further evaluation of the substance
Assessment information

Evaluating competent authority:

-

Assessment outcome:

Successful

Conclusion date:

30/04/2024

Validity of approval

Start date:

01/10/2011

End date:

31/12/2026

Legal act:

Commission Implementing Decision (EU) 2024/734

Documents
Assessment Reports

Assessment Report

AS-RNL_Flocoumafen_PT14_Final Assessment Report.pdf (en)

0034-14_Assessment_Report.pdf (en)

Flocoumafen_PT14_relevant_renewal_data.pdf (en)

Study summaries (Document III-A)

Study summary

Data_003.pdf (en)

Data_006.pdf (en)

Data_004.pdf (en)

Data_001.pdf (en)

Data_011.pdf (en)

Data_007.pdf (en)

Data_008.pdf (en)

Data_010.pdf (en)

Data_002.pdf (en)

Data_005.pdf (en)

Data_012.pdf (en)

Data_009.pdf (en)

Other documents

BPC opinions

Flocoumafen_PT14_Final BPC opinion.pdf (en)

Amendment of active substance - Conclusion Date: 17/01/2022   This item is not a consequence of further evaluation of the substance
Assessment information

Evaluating competent authority:

-

Assessment outcome:

Successful

Conclusion date:

17/01/2022

Validity of approval

Start date:

01/10/2011

End date:

30/06/2024

Legal act:

Reg (EU) 2017/1383

Documents
Assessment Reports

Assessment Report

AS-RNL_Flocoumafen_PT14_Final Assessment Report.pdf (en)

0034-14_Assessment_Report.pdf (en)

Flocoumafen_PT14_relevant_renewal_data.pdf (en)

Study summaries (Document III-A)

Study summary

Data_003.pdf (en)

Data_006.pdf (en)

Data_004.pdf (en)

Data_001.pdf (en)

Data_011.pdf (en)

Data_007.pdf (en)

Data_008.pdf (en)

Data_010.pdf (en)

Data_002.pdf (en)

Data_005.pdf (en)

Data_012.pdf (en)

Data_009.pdf (en)

Other documents

BPC opinions

Flocoumafen_PT14_Final BPC opinion.pdf (en)

Amendment of active substance - Conclusion Date: 10/10/2019   This item is not a consequence of further evaluation of the substance
Assessment information

Evaluating competent authority:

-

Assessment outcome:

Successful

Conclusion date:

10/10/2019

Validity of approval

Start date:

01/10/2011

End date:

30/06/2024

Legal act:

Reg (EU) 2017/1383

Documents
Assessment Reports

Assessment Report

AS-RNL_Flocoumafen_PT14_Final Assessment Report.pdf (en)

0034-14_Assessment_Report.pdf (en)

Study summaries (Document III-A)

Study summary

Data_003.pdf (en)

Data_006.pdf (en)

Data_004.pdf (en)

Data_001.pdf (en)

Data_011.pdf (en)

Data_007.pdf (en)

Data_008.pdf (en)

Data_010.pdf (en)

Data_002.pdf (en)

Data_005.pdf (en)

Data_012.pdf (en)

Data_009.pdf (en)

Other documents

BPC opinions

Flocoumafen_PT14_Final BPC opinion.pdf (en)

Amendment of active substance - Conclusion Date: 11/04/2019   This item is not a consequence of further evaluation of the substance
Assessment information

Evaluating competent authority:

-

Assessment outcome:

Successful

Conclusion date:

11/04/2019

Validity of approval

Start date:

01/10/2011

End date:

30/06/2024

Legal act:

Reg (EU) 2017/1383

Documents
Assessment Reports

Assessment Report

0034-14_Assessment_Report.pdf (en)

Study summaries (Document III-A)

Study summary

Data_003.pdf (en)

Data_006.pdf (en)

Data_004.pdf (en)

Data_001.pdf (en)

Data_011.pdf (en)

Data_007.pdf (en)

Data_008.pdf (en)

Data_010.pdf (en)

Data_002.pdf (en)

Data_005.pdf (en)

Data_012.pdf (en)

Data_009.pdf (en)

Other documents

BPC opinions

Flocoumafen_PT14_Final BPC opinion.pdf (en)

Renewal of active substance - Conclusion Date: 16/10/2017  
Assessment information

Evaluating competent authority:

Netherlands

Assessment outcome:

Successful

Conclusion date:

16/10/2017

Validity of approval

Start date:

01/10/2011

End date:

30/06/2024

Legal act:

Reg (EU) 2017/1383

Documents
Assessment Reports

Assessment Report

0034-14_Assessment_Report.pdf (en)

Study summaries (Document III-A)

Study summary

Data_003.pdf (en)

Data_006.pdf (en)

Data_004.pdf (en)

Data_001.pdf (en)

Data_011.pdf (en)

Data_007.pdf (en)

Data_008.pdf (en)

Data_010.pdf (en)

Data_002.pdf (en)

Data_005.pdf (en)

Data_012.pdf (en)

Data_009.pdf (en)

Other documents
Approval of active substance - Conclusion Date: 25/07/2017  
Assessment information

Evaluating competent authority:

Netherlands

Assessment outcome:

Successful

Conclusion date:

25/07/2017

Validity of approval

Start date:

01/10/2011

End date:

30/09/2016

Legal act:

Directive 2009/150/EC

Documents
Assessment Reports
Study summaries (Document III-A)
Other documents
Amendment of active substance - Conclusion Date: 23/06/2016   This item is not a consequence of further evaluation of the substance
Assessment information

Evaluating competent authority:

-

Assessment outcome:

Successful

Conclusion date:

23/06/2016

Validity of approval

Start date:

01/10/2011

End date:

30/06/2018

Legal act:

Directive 2009/150/EC

Documents
Assessment Reports
Study summaries (Document III-A)
Other documents