MEFENPYR-DIETHYL TECHNICAL MATERIAL
FAO Specification 651.229/TC (May 2011*)
This specification, which is PART ONE of this publication, is based on an evaluation
of data submitted by the manufacturer whose name is listed in the evaluation report
(651.229/2010). It should be applicable to relevant products of these manufacturers
but it is not an endorsement of those products, nor a guarantee that they comply with
the specifications. The specification may not be appropriate for the products of other
manufacturers. The evaluation report (651.229/2010) as PART TWO forms an
integral part of this publication.
1 Description
The material shall consist of mefenpyr-diethyl together with related
manufacturing impurities, in the form of white to beige crystalline powder, and
shall be free from visible extraneous matter and added modifying agents.
2 Active ingredient
2.1 Identity tests (CIPAC CIPAC/4627/A, Note 1)
The safener shall comply with an identity test and, where the identity remains
in doubt, shall comply with at least one additional test.
2.2 Mefenpyr-diethyl content (CIPAC CIPAC/4627/A, Note 1)
The mefenpyr-diethyl content shall be declared (not less than 940 g/kg) and,
when determined, the average measured content shall not be lower than the
declared minimum content.
3 Relevant impurities (Note 2)
Note 1: The reversed phase HPLC method (CIPAC/4627/A) for the determination of mefenpyrdiethyl
in TC, and the normal phase HPLC method (CIPAC/4627/B) for the determination of
mefenpyr-diethyl in WG, OD, EW and EC were adopted by CIPAC in 2008. Prior to their
publication in Handbook N, copies of the methods may be obtained through
http://www.cipac.org/cipacpub.htm
Note 2 There are no relevant impurities to be controlled in products of the manufacturer identified in
evaluation report 651.229/2010. However, ethyl-2-chloro-2-(2,4-dichloro-phenylhydrazono)
acetate may occur as a result of certain manufacturing processes. If this impurity
would occur at ≥ 1 mg/kg (relative to mefenpyr-diethyl) in the products of other
manufacturers, it would be designated as relevant impurity and a clause would be required
to limit its concentration.
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