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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 05/53/EC ,
Reg. (EU) 2018/1262 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2017/1511 ,
Reg. (EU) No 533/2013
Date of approval 01/03/2006 Expiration of approval 31/10/2019
RMS

Co-RMS
SE

FI
Risk Assessment Commission
Category FU Review Report   Thiophanate_methyl_List of studies_2018_final_sanitised.pdf
  Review_Report_thiophanate-methyl.pdf
Remarks The original RMS was Germany.

Extension of approval period: Reg. (EU) 2017/1511
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IT, LT, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK IE
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Thiophanate-methyl (R)
    MRLs Annex II
  • Annex IIIB
Classification Reg. 1272/2008
Skin Sens. 1 - H317 Acute Tox. 4 - H332
Muta. 2 - H341 Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.08 Dir 05/53  
ARfD 0.2 Dir 05/53  
AOEL 0.08 Dir 05/53  
Other
ARfD unnecessary ADI 0,08 JMPR 2006 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level