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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2010/2/EU ,
Reg. (EU) No 540/2011
   
Date of approval 01/12/2009 Expiration of approval 30/11/2021
RMS

Co-RMS
AT

IT
Risk Assessment EFSA
Category PG Review Report   Confirmatory data 2015
  list_Chlormequat.pdf
Remarks Extension of the approval period: Reg. (EU) 2017/555

The original RMS was UK.
Authorisation at national level
Authorised in In progress for
AT, BE, CZ, DE, DK, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, NL, PL, PT, RO, SE, SI, SK, UK BG
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Chlormequat (sum of chlormequat and its salts, expressed as chlormequat-chloride)
    MRLs Annex II
Classification Reg. 1272/2008
Acute Tox. 4 - H302 Acute Tox. 4 - H312
Toxicological information
Reference values Source Remark
ADI 0.04 EFSA 08  
ARfD 0.09 EFSA 08  
AOEL 0.04 EFSA 08  
Other
ARfD 0,05 ADI 0,05 JMPR 2000 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level