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Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 2006/797/EC ,
Reg. (EU) 2017/2065 ,
Reg. (EU) No 540/2011 ,
Reg. (EU) No 993/2011
   
Date of approval 01/01/2012 Expiration of approval 31/12/2021
RMS

Co-RMS
ES

NL
Risk Assessment EFSA
Category FU Review Report   Review Report 2017
  Approval 2011
Type Candidate for Substitution (CfS) CfS - criteria toxic for reproduction 1A / 1B
Authorisation at national level
Authorised in In progress for
CY, ES, FR, IT, MT, PT, SI EL
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • 8-hydroxyquinoline (sum of 8-hydroxyquinoline and its salts, expressed as 8-hydroxyquinoline)
    MRLs Annex IIIA
Classification Reg. 1272/2008
Acute Tox. 3 - H301 Skin Sens. 1 - H317
Eye Dam. 1 - H318 Repr. 1B - H360D
Aquatic Acute 1 - H400 Aquatic Chronic 1 - H410
Toxicological information
Reference values Source Remark
ADI 0.05 Reg. (EU) No 993/2011  
ARfD 0.05 Reg. (EU) No 993/2011  
AOEL 0.05 Reg. (EU) No 993/2011  
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