PLANTS

Language selector

Accessibility tools

Navigation path

Status under Reg. (EC) No 1107/2009 (repealing Directive 91/414/EEC )
Legislation 06/64/EC ,
Reg. (EU) No 2018/524 ,
Reg. (EU) No 540/2011
Old Legislation Reg. (EU) No 678/2014
Date of approval 01/05/2007 Expiration of approval 30/04/2019
RMS

Co-RMS
LT

LV
Risk Assessment EFSA
Category PG Review Report   List of studies 2018
  Review Report 2006
Remarks Extention of the approval (Reg (EU)2018/524)
The original RMS was the Netherlands.
Authorisation at national level
Authorised in In progress for
AT, BE, BG, CZ, DE, DK, EE, EL, ES, FI, FR, HR, HU, IE, IT, LT, LU, LV, MT, NL, PL, PT, RO, SE, SI, SK, UK
EU - Maximum Residue Levels (Reg. (EC) No 396/2005) (MRLs)
Legislation Annexes
  • Trinexapac (sum of trinexapac (acid) and its salts, expressed as trinexapac)
    MRLs Annex II
Classification Reg. 1272/2008
No classification
Toxicological information
Reference values Source Remark
ADI 0.32 Dir 06/64  
ARfD Not applicable Dir 06/64  
AOEL 0.34 Dir 06/64  
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