6-メチルキノキサリン-2,3-ジチオール2,3-カルボナート 化学特性,用途語,生産方法
外観
白色～うすい黄色, 結晶～粉末
溶解性
水に不溶 (1mg/l at 20℃)。トルエン20g/l, ジクロロメタン40g/l, ヘキサン1.8g/l, イソプロパノール0.9g/l, シクロヘキサノン18g/l, ジメチルホルムアミド10g/l at 20℃。トルエンにやや溶けにくく、ヘキサンに溶けにくい。
農薬用途
殺虫剤、殺菌剤、ダニ駆除剤
化学的特性
Chinomethionate is a tan to yellow crystals. Soluble in benzene, toluene, and dioxane; insoluble in water. It has been shown to have low toxicity to mammals, birds and bees, but is highly toxic to fish and some aquatic invertebrates.
定義
ChEBI: A dithioloquinoxaline that results from the formal condensation of 6-methylquinoxaline-2,3-dithiol with phosgene. It has been used as a fungicide and acaricide for the control of mites and powdery mildew on citrus, vegetables, and walnuts, but is not appro
ed for use in the EU.
一般的な説明
Yellow crystals. Non-corrosive. Used as a selective fungicide.
空気と水の反応
Hydrolyzed in alkaline solution.
反応プロフィール
A member of the quinoxaline, dithiolane family.
危険性
Toxic by ingestion and inhalation.
安全性プロファイル
Moderately toxic by intraperitoneal, ingestion, and skin contact routes. A pesticide. When heated to decomposition it emits very toxic fumes of NOx and SOx.
環境運命予測
Chemical/Physical. Reacts with ammonia forming 6-methyl-2,3-quinoxalinedithiol.
代謝経路
Limited information is available to describe the degradation and metabolic
fate of chinomethionat. Hydrolytic cleavage of the dithiocarbonate
ring is the primary degradation reaction in water, plants and animals.
6-メチルキノキサリン-2,3-ジチオール2,3-カルボナート 上流と下流の製品情報
原材料
準備製品