ジチオりん酸O,O-ジメチルS-(α-エトキシカルボニルベンジル)

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

  H302：飲み込むと有害

  H312：皮膚に接触すると有害

  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

  P264：取扱い後は皮膚をよく洗うこと。

  P264：取扱い後は手や顔をよく洗うこと。

  P270：この製品を使用する時に、飲食または喫煙をしないこ 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。

  P301+P312：飲み込んだ場合：気分が悪い時は医師に連絡する こと。

  P302+P352：皮膚に付着した場合：多量の水と石鹸で洗うこと。

  P312：気分が悪い時は医師に連絡すること。

  P322：特別な処置が必要である（このラベルの．．． を見よ）。

  P330：口をすすぐこと。

  P363：汚染された衣類を再使用す場合には洗濯をすること。

  P391：漏出物を回収すること。

  P501：内容物/容器を．．．に廃棄すること。

ジチオりん酸O,O-ジメチルS-(α-エトキシカルボニルベンジル) 価格

MSDS Information

• Phenthoate

ジチオりん酸O,O-ジメチルS-(α-エトキシカルボニルベンジル) 化学特性,用途語,生産方法

• 外観

  無色～うすい黄色, 澄明の液体

• 溶解性

  エタノール及びアセトンに溶けやすく、水にほとんど溶けない。

• 農薬用途

  殺虫剤、ダニ駆除剤

• 説明

  Phenthoate is a colorless crystalline substance. Solubility in water is 10 mg/L (25 ?C). It is readily soluble in most organic solvents. Log Kow = 3.69. It is relatively stable in neutral and acidic aqueous media but decomposed under alkaline conditions.

• 使用

  Phenthoate is an organothiophosphate insecticide used against lepidoptera and houseflies.

• 定義

  ChEBI: An organic thiophosphate that is ethyl mandelate in which the hydroxy group has been replaced by a (dimethoxyphosphorothioyl)sulfanediyl group.

• 代謝経路

  Studies which have measured the degradation of phenthoate in buffered aqueous solution have shown that it can be hydrolysed at the carboethoxy group, by cleavage of the P-S and C-S bonds and by demethylation in addition to oxidative desulfuration to the oxon. Reports on the metabolism of phenthoate in plants, insects and mammals have shown that the metabolic products can be largely explained by cleavage of these reactive groups. P-S and C-S bond cleavage is demonstrated by the formation of both O,O-dimethyl phosphorothioate and O,O-dimethyl phosphorodithioate. Metabolism in plants, insects and mammals is similar with many of the possible metabolites being identified in most species. Phenthoate carboxylic acid is a major metabolite except in plants where hydrolysis of the phosphorodithioate moiety predominates. In mammals, little or none of the activated metabolite, phenthoate oxon, can be detected, suggesting that the predominant metabolic route is degradative, wkuch may in part explain the favourable mammalian toxicity of the compound.

• 代謝

  Phenthoate is degraded by hydrolysis of the carboethoxy moiety. Demethylation and the cleavage of P?S?C linkages are also important degradation routes. Oxidative desulfuration to the oxon followed by hydrolysis occurs in animals and plants.The major metabolites excreted in the urine and feces are demethyl phenthoate, demethyl phenthoate acid, demethyl phenthoate oxon, and O,O-dimethyl hydrogen phosphorodithioate and phosphorothioate. It is rapidly degraded in soils; DT₅₀ was less than 1 d in both upland and submerged soil.

ジチオりん酸O,O-ジメチルS-(α-エトキシカルボニルベンジル) 上流と下流の製品情報

ジチオりん酸O,O-ジメチルS-(α-エトキシカルボニルベンジル) スペクトルデータ(¹HNMR、¹³CNMR、IR1、MS)

2597-03-7, ジチオりん酸O,O-ジメチルS-(α-エトキシカルボニルベンジル) キーワード