Основные атрибуты  химическое свойство Информация о безопасности химические свойства, назначение, производство запасные части и сырье поставщик Обзор
ТРИФЛУМИЗОЛ структурированное изображение

ТРИФЛУМИЗОЛ

  • английское имяTriflumizole
  • CAS №99387-89-0
  • CBNumberCB91120821
  • ФормулаC15H15ClF3N3O
  • мольный вес345.75
  • файл Mol99387-89-0.mol
химическое свойство
давление пара 1.86 x 10-4 Pa (25 °C )
пка 3.7 (base)
Растворимость в воде 12.5 x 103 mg l-1(20 °C )
FDA UNII 7J6Y4H9MV5
Система регистрации веществ EPA 1H-Imidazole, 1-[(1E)-1-[[4-chloro-2-(trifluoromethyl) phenyl]imino]-2-propoxyethyl]- (99387-89-0)
Пестициды Закон о свободе информации (FOIA) Triflumizole
Заявления об опасности и безопасности
РИДАДР 3077
Класс опасности 9
Группа упаковки III

ТРИФЛУМИЗОЛ химические свойства, назначение, производство

Использование

Triflumizole is used for the control of Gymnospurangum and Venturia spp. in pome fruit, against powdery Erysiphaceae in fruit and vegetables, and against Fusarium, Fulvia and Monilia spp. It is also used as a seed treatment against Helminthospurium, Tilletia and Ustilago spp. in cereals.

Метаболический путь

Triflumizole is unstable in aqueous solution when exposed to light and it is readily metabolised by plants and animals. The primary route of metabolism is by cleavage of the imidazole ring to give several metabolites which retain the 4-chloro-2-trifluoromethylaniline moiety. The major metabolite in crops, 2, is formed by loss of the imidazole ring.

Деградация

Aqueous solutions of triflumizole are degraded by sunlight with a DT50 of 29 hours. The sole hydrolysis product of triflumizole in the dark is 2, which is formed by loss of the imidazole ring.
The major product of photolysis of triflumizole is 4, which is probably formed in the presence of oxygen via 3. This compound was soluble in the solid state but decomposed in solution, even if stored in a refrigerator (Hashimoto et al., 1990).

ТРИФЛУМИЗОЛ запасные части и сырье

запасной предмет

ТРИФЛУМИЗОЛ поставщик

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