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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 04/99/EC ,
Reg. (EU) 2018/524 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) 2016/2016
Date of approval 01/01/2005 Expiration of approval 30/04/2019
RMS

Co-RMS
UK

DE
Risk Assessment Commission
Category IN Review Report
Remarks Extension of the approval period (Reg. (EU) 2018/524)
Type Candidate for Substitution (CfS) CfS - criteria endocrine disrupting properties
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, NL, PL, PT, RO, SE, SI, SK, UK
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Acute Tox. 4 - H332
STOT SE 3 - H336 Carc. 2 - H351
Repr. 1B - H360FD Aquatic Acute 1 - H400
Aquatic Chronic 1 - H410  
Toxicological information
Reference values Source Remark
ADI 0.01 04/99/EC  
ARfD 0.03 04/99/EC  
AOEL 0.02 04/99/EC  
Other
ARfD 0,03 - ADI 0,01 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