Buprofezin химические свойства, назначение, производство
Использование
Buprofezin is a insecticide which works as a chitin synthesis inhibitor. Buprofezin is used to control stubborn rice pests and is effective in controlling green leaf hoppers and white back plant hoppe
rs for long durations.
Опасность
Moderately toxic by ingestion. Low toxic-
ity by skin contact.
Сельскохозяйственное использование
Insecticide, Acaricide, Insect growth regulator: For insect control in food crops and greenhouse
ornamentals.
Торговое название
APPLAUD®; NNI-750®
Фармаколо?гия
The foregoing indicates that the modes of action of
buprofezin and benzoylureas could be similar or identical.
However, one differing biochemical effect of buprofezin is
inhibition of prostaglandin biosynthesis (33), a mechanism
that has been suggested as responsible for its ovicidal
activity. Subsequently, the in vitro and in vivo effects of
buprofezin were found to be strongly antagonized by 20-
hydroxyecdysone (34), which also affected prostaglandin
biosynthesis. Thus, inhibition of both prostaglandin and
chitin biosynthesis by buprofezin was prevented by 20-
hydroxyecdysone, so that both effects of the insecticide
are mediated via an effect on the hormone concentration
or its receptor. Consequently, buprofezin seems to inhibit
the drop in the 20-hydroxyecdysone titer that triggers
epidermal cell proliferation, old cuticle digestion, and new
cuticle deposition, but the detailed mechanism of this
action has yet to be established.
Метаболический путь
Buprofezin gradually decomposes in soils under
flooded and upland conditions, with half-lives of
104 and 80 days, respectively. After 150 days, five
degradation products are identified as 2-tert-
butylimino-5-(4-hydroxyphenyl)-3-isopropylperhydro-
1,3,5-thiadiazin-4-one, 3-isopropyl-5-phenylperhydro-
1,3,5-thiadiazin-2,4-dione, 1-tert-butyl-3-ispropyl-5-
phenylbiuret, 1-isopropyl-3-phenylurea, and
phenylurea. As minor products, 2-tert-butylimino-5-
phenylperhydro-1,3,5-thiadiazin-4-one or buprofezin
sulfoxide are found in the flooded or in the upland
soils. Since neither formation of 14CO2 nor
hydroxylation is observed in the sterile soils,
buprofezin seems to have undergone complete
mineralization in soils under both conditions through
biological transformation by soil microorganisms.
Buprofezin препаратная продукция и сырье
сырьё
препарат