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Active substance factsheet - Last updated: 21/11/2019

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

MAXFORCE PLATIN

Belgium

Denmark

France

Germany

Ireland

Luxembourg

Netherlands

Slovenia

Spain

Sweden

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