テフルトリン

危険有害性情報のコード(GHS)

• 絵表示(GHS)

  

• 注意喚起語

  Danger

• 危険有害性情報

  H410：長期的影響により水生生物に非常に強い毒性

• 注意書き

  P260：粉じん/煙/ガス/ミスト/蒸気/スプレーを吸入しないこ と。

  P262：眼、皮膚、衣類につけないこと。

  P273：環境への放出を避けること。

  P280：保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。

テフルトリン 価格

テフルトリン 化学特性,用途語,生産方法

• 外観

  白色〜ほとんど白色, 結晶性粉末〜粉末

• 溶解性

  水に殆ど不溶。有機溶媒に易溶。水0.02mg/l(pH 5.9, 20℃)。アセトン,ヘキサン, トルエン, ジクロロメタン, 酢酸エチル＞500, メタノール263。(全てg/l 21℃)。アセトンに溶け、水にほとんど溶けない。

• 用途

  合成ピレスロイド土壌害虫の防除に使用

• 農薬用途

  殺虫剤

• 化学的特性

  Pale Yellow Low Melting Solid

• 使用

  Tefluthrin is a pyrethroid based insecticide. Tefluthrin is used in the control of a broad range of soil pests, including members of the Coleoptera, Lepidoptera, and Diptera.

• 定義

  ChEBI: A cyclopropanecarboxylate ester resulting from the formal condensation of the carboxy group of 3-[(1Z)-2-chloro-3,3,3-trifluoroprop-1-en-1-yl]-2,2-dimethylcyclopropanecarboxylic acid with the hydroxy group of 2,3,5,6-tetrafluoro-4-methylbe zyl alcohol.

• 作用机制

  昆虫の神経軸索の電位依存性ナトリウムチャンネルを遮断して昆虫を致死させる

• 农业用途

  Insecticide, Miticide: A U.S. EPA restricted use Pesticide (RUP). Registered in the U.S. for use on corn. Elsewhere it is registered for use on a variety of crops, e.g., peanuts, sweet potato, sugarcane, cabbage, radish, Brussels sprouts, and strawberries. Registered for use in EU countries.

• 製品名

  FORCE®; FORCE® ST; FORZA®; JF 6064®; KOMET-RP®; PP 993®; R 151993®

• 薬理学

  The commercialized compound, tefluthrin, was recommended to control soil-inhabiting pests (28). The most salient feature of the compound, which justifies its use exclusively for better performance of tefluthrin as a soil insecticide compared with cyhalothrin, is its approximately four orders ofmagnitude higher vapor pressure (V.P. = 8.4 vs. 0.001 mPa; see Table 6). Beside the quick insecticidal action attributed to fast penetration, tefluthrin also displays toxic symptoms at its sublethal dose, which could play an important role in field performance (179). The most active configuration of tefluthrin, (Z)(1RS)-cis-isomer mixture, is the optically active (Z)(1R)-cis-isomer.

• 代謝経路

  When a goat is dosed with 14C-tefluthrin orally, extensive metabolism occurs in the goat by ester cleavage and oxidation at a variety of positions on the molecules. Low radioactive residues are detected in the milk, fat, and muscle, with tefluthrin as the largest individual component of the residue. Higher residues are present in the kidney and liver, and only a small percentage of this residue is due to tefluthrin. The remainder in the kidney and liver is a complex mixture of metabolites. In total, eight metabolites are identified in the feces and urine as well as other tissues such as fat, muscle, kidney, and liver.

テフルトリン 上流と下流の製品情報

79538-32-2, テフルトリン キーワード