N-[(ジエトキシチオホスフィノイルチオ)アセチル]-N-メチルカルバミド酸エチル

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

  H311：皮膚に接触すると有毒

  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。

  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。

  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。

N-[(ジエトキシチオホスフィノイルチオ)アセチル]-N-メチルカルバミド酸エチル 価格

N-[(ジエトキシチオホスフィノイルチオ)アセチル]-N-メチルカルバミド酸エチル 化学特性,用途語,生産方法

• 外観

  わずかにうすい黄色～褐色, 液体

• 溶解性

  エタノール及びアセトンに溶け、水にほとんど溶けない。

• 農薬用途

  殺虫剤

• 使用上の注意

  アルゴン封入

• 説明

  Mecarbam is a pale yellow to light brown oil, bp 144 ?C/0.02 mm Hg. It is slightly soluble in water (<0.1% at 25 ?C) and miscible with most organic solvents except alkanes. Log Kow = 2.6. It is readily hydrolyzed in aqueous media below pH 3.

• 化学的特性

  Yellow oil.

• 使用

  Mecarbam is an organothiophosphate acaricides used to control powdery mildew of cucumbers.

• 定義

  ChEBI: An organic thiophosphate that is O,O-diethyl hydrogen phosphorodithioate in which the hydrogen attached to a sulfur is replaced by a 2-[(ethoxycarbonyl)(methyl)amino]-2-oxoethyl group.

• 危険性

  Highly toxic, cholinesterase inhibitor. Use may be restricted.

• 代謝経路

  Mecarbam in a close chemical analogue of dimethoate and it is photolytically decarboxyethylated to the diethyl analogue of dimethoate. The main route of hydrolytic decomposition in moderately basic solution is via attack on the S-methylene carbon atom rather than on phosphorus or the carbamoyl group, followed by cleavage of the S-C bond yielding O,Odiethyl phosphorodithioate as the main product. Mecarbam oxon has been reported as a metabolite in plants and animals but few detailed studies have been reported on the metabolic or environmental fate of mecarbam.

• 代謝

  In mammals, mecarbam is rapidly metabolized by hydrolysis, oxidative desulfuration to the oxon, and degradation of the carbamoyl moiety. O-Deethylation also takes place to a minor extent. In soil, it persists for 4–6 weeks.

2595-54-2, N-[(ジエトキシチオホスフィノイルチオ)アセチル]-N-メチルカルバミド酸エチル キーワード