3-tert-ブチル-1-(4-フェノキシ-2,6-ジイソプロピルフェニル)チオ尿素

危険有害性情報のコード(GHS)

• 絵表示(GHS)

  

• 注意喚起語

  Warning

• 危険有害性情報

  H332：吸入すると有害

• 注意書き

  P261：粉じん/煙/ガス/ミスト/蒸気/スプレーの吸入を避ける こと。

  P271：屋外または換気の良い場所でのみ使用すること。

3-tert-ブチル-1-(4-フェノキシ-2,6-ジイソプロピルフェニル)チオ尿素 価格

3-tert-ブチル-1-(4-フェノキシ-2,6-ジイソプロピルフェニル)チオ尿素 化学特性,用途語,生産方法

• 外観

  白色, 結晶性粉末〜粉末

• 溶解性

  水に不溶 (0.06mg/l at 25℃), エタノール43g/l, アセトン320g/l, トルエン330g/l, n-ヘキサン9.6g/l, n-オクタノール26g/l at 25℃。アセトンに溶けやすく、エタノールにやや溶けやすく、水にほとんど溶けない。

• 農薬用途

  殺虫剤

• 説明

  Diafenthiuron is a broad spectrum acaricide and insecticide, diafenthiuron is registered for use on cotton, soybeans, vegetables, fruit and ornamentals. It controls all post-hatch stages of mites, whiteflies and aphids. Its ability to control all sucking pests of cotton as well as mites, with no known toxicity to beneficial insects, is unique and very valuable in cotton integrated pest management (IPM) programs.

• 使用

  Diafenthiuron is an insecticide.

• 毒性学

  Diafenthiuron has low toxicity to birds, mammals and beneficial insects, and is only slightly toxic to predatory mites. It is toxic to fish, but presents little hazard because it is rapidly degraded.

• Mode of action

  Diafenthiuron is a proinsecticide, which means that it must be converted to another compound – the drug – in order to be toxic. Activation of diafenthiuron to its carbodiimide drug occurs on the leaf surface, catalyzed by light, or in the insect, catalyzed by P450 monooxygenases. Diafenthiuron carbodiimide binds to the glutamate residue in the transmembrane F0 subunit of ATP synthase where protons from the intermembrane space dock to begin their journey across the inner mitochondrial membrane. Binding of diafenthiuron carbodiimide to this site blocks proton transport and ATP synthesis. Diafenthiuron was launched in 1991 and resistance has not yet been reported.

3-tert-ブチル-1-(4-フェノキシ-2,6-ジイソプロピルフェニル)チオ尿素 上流と下流の製品情報

3-tert-ブチル-1-(4-フェノキシ-2,6-ジイソプロピルフェニル)チオ尿素 生産企業

Global(209)Suppliers

80060-09-9, 3-tert-ブチル-1-(4-フェノキシ-2,6-ジイソプロピルフェニル)チオ尿素 キーワード