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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2008/69 ,
Reg. (EU) No 1100/2011 ,
Reg. (EU) No 540/2011
   
Date of approval 01/01/2009 Expiration of approval 31/12/2018
RMS

Co-RMS
ES

UK
Risk Assessment EFSA
Category FU Review Report   Specifications 2013
  Update 2011
  Correction 2012
Remarks Substance fulfilling criteria Annex V Reg 1490/2002

The original RMS was Sweden.
Type Candidate for Substitution (CfS) CfS - criteria two PBT criteria
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CY, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.01 Dir 08/69  
ARfD 0.16 Dir 08/69  
AOEL 0.16 Dir 08/69  
Other
 
Legend
  • RMS:Rapporteur Member State
  • Co-RMS:Co-Rapporteur Member State
  • ADI:Acceptable daily intake
  • ARfD:Acute reference dose
  • AOEL:Acceptable operator exposure level