4,6-ジクロロ-N-(o-クロロフェニル)-1,3,5-トリアジン-2-アミン 化学特性,用途語,生産方法
外観
白色, 結晶～粉末
溶解性
水に不溶。水8mg/l(20℃)。アセトン100, クロロベンゼン60,トルエン50, キシレン40(全てg/l 30℃)。ジクロロメタン90,イソプロパノール8, ヘキサン1.7(全てg/l 20℃)。
用途
失効農薬、抗真菌薬、窒素複素環系殺菌剤
農薬用途
殺菌剤
化学的特性
white to light brown crystals or powder
使用
Pesticide used to control fungus diseases in lawns and turf.
定義
ChEBI: A member of the class of triazenes that is dichlorotriazene in which the hydrogen is replaced by an o-chloroanilino group. A fungicide formerly used to control leaf spots and downy mildew, it is no longer approved for use within the European U
ion.
一般的な説明
White to tan crystals or white powder. Moderately soluble in organic solvents. Insoluble in water. Melting point 159°C.
空気と水の反応
Insoluble in water. Stable in neutral and slightly acidic aqueous media but hydrolyzes on heating with alkali.
反応プロフィール
ANILAZINE is incompatible with oils and alkalis. ANILAZINE is slightly corrosive to metals.
火災危険
Flash point data for ANILAZINE are not available; however, ANILAZINE is probably combustible.
環境運命予測
Soil. Anilazine is readily degraded by soil bacteria (Harris et al., 1968). The reported
half-life of anilazine in soil is approximately 12 hours (Hartley and Kidd, 1987)
Plant. In plants, one or both of the chlorine atoms on the triazine ring may be replaced
by thio or amino groups (Hartley and Kidd, 1987)
Chemical/Physical. Anilazine is subject to hydrolysis (Windholz et al., 1983) releasing
chlorine gas (Hartley and Kidd, 1987)
4,6-ジクロロ-N-(o-クロロフェニル)-1,3,5-トリアジン-2-アミン 上流と下流の製品情報
原材料
準備製品