rac-2β*-(2-メチルベンジルオキシ)-4α*-イソプロピル-1α*-メチル-7-オキサビシクロ[2.2.1]ヘプタン

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

  H411：長期的影響により水生生物に毒性

• 注意書き

  P273：環境への放出を避けること。

rac-2β*-(2-メチルベンジルオキシ)-4α*-イソプロピル-1α*-メチル-7-オキサビシクロ[2.2.1]ヘプタン 価格

rac-2β*-(2-メチルベンジルオキシ)-4α*-イソプロピル-1α*-メチル-7-オキサビシクロ[2.2.1]ヘプタン 化学特性,用途語,生産方法

• 外観

  ごくうすい黄色〜黄色, 液体

• 溶解性

  アセトンに溶け、水にほとんど溶けない。

• 農薬用途

  除草剤

• 説明

  Cinmethylinwas developed by Shell Chemical Company in the early 1980s as a weed control agent for monocotyledonous species. This herbicide controls important grasses such as green foxtail (Setaria viridis) and barnyardgrass (Echinochloa crus-galli) and suppresses the growth of several broadleaf weeds such as prickly sida (Sida spinosa) and velvetleaf (Abutilon theophrasti).

• 使用

  Cinmethylin is used as pre-emergence grass herbicide. Cinmethylin is member of the cineole eucalyptol family.

• 薬理学

  Cinmethylin is active on several important grasses in rice (Echinochloa spp., Cyperus spp., and Monochoria vaginalis) at rates from 25 to 100 g ai/ha (5). Its chemical and toxicological features (low persistence in environment and low mammalian toxicity) generated a significant level of interest in its use as a rice herbicide.

• 代謝経路

  When rats are administered 14C-cinmethylin orally, the major route of its elimination is via urinary excretion. A complex degradation pattern of cinmethylin is observed and the metabolic pathways involve hydroxylation, oxidation at the benzyl and cineol portions, conjugation with glucuronic acid and glycine, and cleavage of the ether linkage. When rats are administered 14C-cinmethylin by stomach incubation, two minor metabolites are identified as o- (acetoxymethyl)benzoic acid and 9-(acetoxymethyl)-a- carboxycinmethylin.

rac-2β*-(2-メチルベンジルオキシ)-4α*-イソプロピル-1α*-メチル-7-オキサビシクロ[2.2.1]ヘプタン 上流と下流の製品情報

rac-2β*-(2-メチルベンジルオキシ)-4α*-イソプロピル-1α*-メチル-7-オキサビシクロ[2.2.1]ヘプタン 生産企業

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87818-31-3, rac-2β*-(2-メチルベンジルオキシ)-4α*-イソプロピル-1α*-メチル-7-オキサビシクロ[2.2.1]ヘプタン キーワード