4-クロロ-N-[(E)-1-(1H-イミダゾール-1-イル)-2-プロポキシエチリデン]-2-(トリフルオロメチル)アニリン

4-クロロ-N-[(E)-1-(1H-イミダゾール-1-イル)-2-プロポキシエチリデン]-2-(トリフルオロメチル)アニリン 価格

4-クロロ-N-[(E)-1-(1H-イミダゾール-1-イル)-2-プロポキシエチリデン]-2-(トリフルオロメチル)アニリン 化学特性,用途語,生産方法

• 農薬用途

  殺菌剤

• 使用

  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.

• 代謝経路

  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.

• Degradation

  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).

4-クロロ-N-[(E)-1-(1H-イミダゾール-1-イル)-2-プロポキシエチリデン]-2-(トリフルオロメチル)アニリン 上流と下流の製品情報

4-クロロ-N-[(E)-1-(1H-イミダゾール-1-イル)-2-プロポキシエチリデン]-2-(トリフルオロメチル)アニリン 生産企業

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