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Active substance factsheet - Last updated: 14/02/2020

Active substance

Substance name:

(E)-1-(2-Chloro-1,3-thiazol-5-ylmethyl)-3- methyl-2-nitroguanidine (Clothianidin)

EC number:

433-460-1

CAS number:

210880-92-5

IUPAC name:

(E)-N'-[(2-chloro-1,3-thiazol-5-yl)methyl]-N-methyl-N''-nitroguanidine

BAS number:

15

Product-type:

PT18

Candidate for substitution:

Yes

Regulatory Process:

Review programme substance

Approval/Assessment status:

Approved

Related authorised biocidal products

1 related product

Trade name
Market area
Autorisation Type

-

CLOTHIANIDIN RB1

Clothianidin RB 1

MAXFORCE PLATIN

SOLFAC GEL BARATAS

Austria

Belgium

Denmark

France

Germany

Greece

Ireland

Luxembourg

Netherlands

Portugal

Slovenia

Spain

Sweden

Switzerland

United Kingdom

 National authorisation Link to the factsheet
Approval data details
Administrative identifiers

Evaluating competent authority:

Germany

R4BP asset number:

EU-0012168-0000

Approval identifiers

Legal act:

REGULATION (EU) 2015/985

Validity of approval

Start date:

01/10/2016

End date:

30/09/2026

Documents
Assessment Reports

Assessment Report

0015-18_Assessment_Report.pdf (en)

Study summaries (Document III-A)
Other documents

BPC opinions

Clothianidin_PT18_Final BPC opinion.pdf (en)

Amendment of active substance - Conclusion Date: 11/04/2019
Assessment information

Evaluating competent authority:

European Commission

Assessment outcome:

Successful

Conclusion date:

11/04/2019

Validity of approval

Start date:

01/10/2016

End date:

30/09/2026

Legal act:

REGULATION (EU) 2015/985

Documents
Assessment Reports

Assessment Report

0015-18_Assessment_Report.pdf (en)

Study summaries (Document III-A)
Other documents

BPC opinions

Clothianidin_PT18_Final BPC opinion.pdf (en)

Amendment of active substance - Conclusion Date: 24/07/2015
Assessment information

Evaluating competent authority:

European Commission

Assessment outcome:

Successful

Conclusion date:

24/07/2015

Validity of approval

Start date:

01/10/2016

End date:

30/09/2026

Legal act:

REGULATION (EU) 2015/985

Documents
Assessment Reports

Assessment Report

0015-18_Assessment_Report.pdf (en)

Study summaries (Document III-A)
Other documents
Approval of active substance - Conclusion Date: 14/07/2015
Assessment information

Evaluating competent authority:

Germany

Assessment outcome:

Successful

Conclusion date:

14/07/2015

Validity of approval

Start date:

01/10/2016

End date:

30/09/2026

Legal act:

REGULATION (EU) 2015/985

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