チオりん酸O,O-ジエチルO-(1-フェニル-1H-1,2,4-トリアゾール-3-イル)

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

  H301：飲み込むと有毒

  H312：皮膚に接触すると有害

  H330：吸入すると生命に危険

  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

  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。

チオりん酸O,O-ジエチルO-(1-フェニル-1H-1,2,4-トリアゾール-3-イル) 価格

MSDS Information

• Phenyl-1,2,4-triazolyl-3-(O,O-diethyl thionophosphate)

チオりん酸O,O-ジエチルO-(1-フェニル-1H-1,2,4-トリアゾール-3-イル) 化学特性,用途語,生産方法

• 外観

  ごくうすい黄色〜赤みの黄色, 澄明の液体

• 溶解性

  水30～40mg/kg(20℃)。アセトン, 酢酸エチル＞1,000,エタノール, トルエン＞330, ヘキサン9(全てg/kg)。

• 用途

  有机磷类殺虫

• 農薬用途

  殺虫剤、ダニ駆除剤、線虫駆除剤

• 使用

  Triazophos is used to control chewing and sucking insects and mites in a wide range of crops. It is also used to control some nematodes in ornamentals and strawberries.

• 一般的な説明

  Yellowish oil. Used to control insects, mites, and nematodes. Not registered as a pesticide in the U.S.

• 反応プロフィール

  Organophosphates, such as Triazophos, are susceptible to formation of highly toxic and flammable phosphine gas in the presence of strong reducing agents such as hydrides. Partial oxidation by oxidizing agents may result in the release of toxic phosphorus oxides.

• 健康ハザード

  This is an organophosphate pesticide. Triazophos is a cholinesterase inhibitor and acts on the central nervous system. Organic phosphorus insecticides are absorbed by the skin as well as by the respiratory and gastrointestinal tracts.

• 火災危険

  This is an organophosphate pesticide. Some of these materials may burn but none of them ignite readily. Container may explode in heat of fire. Fire may produce irritating or poisonous gases. Degraded by acids and alkalis.

• 农业用途

  Insecticide: Triazophos is a broad-spectrum insecticide and acaricide used to control sucking and chewing pests on a variety of crops, including cotton, rice, corn, beets and fruit trees. Not currently registered for use in the U.S. Not approved for use in EU countries . There are more than 30 global suppliers .

• 製品名

  HILAZPOPHOS®; HOE 2960 OJ®; HOE 002960®; HOSTATHION®; SUTATHION®

• 代謝経路

  The main route of biotransformation of triazophos is degradation to 1- pheny1-3-hydroxy-1,2,4-triazole, probably either via hydrolysis of triazophos oxon or through oxidative cleavage of triazophos itself. The triazole ring of this metabolite is opened to give 1-phenylsemicarbazide and semicarbazide, both of which are conjugated in the rat and also degraded to urea as the main urinary metabolite.

チオりん酸O,O-ジエチルO-(1-フェニル-1H-1,2,4-トリアゾール-3-イル) 上流と下流の製品情報

チオりん酸O,O-ジエチルO-(1-フェニル-1H-1,2,4-トリアゾール-3-イル) 生産企業

Global(226)Suppliers

24017-47-8, チオりん酸O,O-ジエチルO-(1-フェニル-1H-1,2,4-トリアゾール-3-イル) キーワード