Fenpropathrin химические свойства, назначение, производство
Использование
Fenpropathrin controls many species of mites and insects on pome
fruit, citrus, vines, hops, vegetables, cotton, ornamentals and glasshouse
crops such as tomatoes.
Метаболический путь
Fenpropathrin possesses only one chiral centre (at benzylic carbon) and
therefore presents a much simpler stereochemical picture than that seen
with most of the other pyrethroids. Most metabolic work has been conducted
with the RS racemate. Solution and surface photochemistry, and
degradation in water, soils, plants and animals, have been reported. The
fate of the 3-phenoxybenzyl portion of the molecule is very similar to that
reported for cypermethrin and other analogues. Degradation is mainly by
ester cleavage and hydroxylation.
Fenpropathrin препаратная продукция и сырье
сырьё
препарат