1-[(o-クロロフェニル)スルホニル]-3-(4-メトキシ-6-メチル-1,3,5-トリアジン-2-イル)尿素

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

  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

  P273：環境への放出を避けること。

  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。

1-[(o-クロロフェニル)スルホニル]-3-(4-メトキシ-6-メチル-1,3,5-トリアジン-2-イル)尿素 価格

MSDS Information

• Telar

1-[(o-クロロフェニル)スルホニル]-3-(4-メトキシ-6-メチル-1,3,5-トリアジン-2-イル)尿素 化学特性,用途語,生産方法

• 外観

  白色, 結晶〜粉末

• 溶解性

  水300(pH5)、27900(pH7)(mg/l、25℃)。ジクロロメタン102、アセトン57、メタノール14、トルエン3、ヘキサン＜0.01(g/l、22℃)。メタノールに溶ける。

• 農薬用途

  除草剤

• 説明

  Chlorsulfuron is one of the first sulfonylurea herbicides developed and commercialized by DuPont. Dr George Levitt and his team at DuPont first synthesized chlorsulfuron in 1976, and it was commercialized for use as a herbicide in 1981. It is currently registered by DuPont in the United States, Canada, the European Union, Russia, the Ukraine, Australia, New Zealand, South Africa, Saudi Arabia, and in several countries of South America.
  Compared with many other herbicides that are applied at levels of pounds per acre (or kilograms per acre), sulfonylureas are highly effective at use rates of less than an ounce per acre (approximately 6 g per acre for chlorsulfuron).

• 化学的特性

  Colorless, odorless crystals

• 使用

  Chlorsulfuron is used as a postemergence herbicide for the control of dicotyledonous weeds, with excellent safety for wheat and other cereals crops. While chlorsulfuron is primarily used to control weeds in cereals, it can also be used in range and pasture applications. It is currently only used to a minor extent for nonfood industrial applications and right-of-way purposes.

• 一般的な説明

  Colorless crystals. Non corrosive. Insoluble in water. Used as an herbicide.

• 空気と水の反応

  Insoluble in water. Reacts slowly with water. The reaction is promoted by acid such that the pH is less than 5.0 (1/2 life of 24-48 hrs.). Reaction is also promoted by polar organic solvents such as methanol and acetone.

• 作用机制

  アセト乳酸合成酵素（ALS）を阻害する

• 农业用途

  Herbicide: A selective systemic herbicide used to control most broadleaf weeds and some annual grasses in wheat, barley, oats, duram, rye, triticale and flax. Applied to non-crop sites such as rights-of-way, fence rows and roadsides.

• 製品名

  DPX 4189®; FINESSE®; GLEAN®; GLEAN 20DF®; LANDMARK® MP; LASHER®; RIVERDALE CORSAIR®; TELAR® DF

• 職業ばく露

  A selective systemic sulfonylurea herbicide used to control most broadleaf weeds and some annual grasses in wheat, barley, oats, duram, rye, triticale, and flax. Applied to noncrop sites such as rights-of-way, fence rows, and roadsides.

• 環境運命予測

  Soil. Degrades in soil via hydrolysis followed by microbial degradation forming low molecular weight, inactive compounds. The estimated half-life was reported to range from 4 to 6 weeks (Hartley and Kidd, 1987; Cremlyn, 1991). Microorganisms capable of degrading chlorsulfuron are Aspergillis niger, Streptomyces griseolus and Penicillium sp. (Humburg et al., 1989). One transformation product reported in field soils is 2-chlorobenzenesulfonamide (Smith, 1988)
  The reported dissipation rate of chlorsulfuron in surface soil is 0.024/day (Walker and Brown, 1983). The persistence of chlorsulfuron decreased when soil temperature and moisture were increased (Walker and Brown, 1983; Thirunarayanan et al., 1985)
  Plant. Chlorsulfuron is metabolized by plants to hydroxylated, nonphytotoxic compounds including 2-chloro-N-(((4-methoxy-6-methyl-1,3,5-triazin-2-yl)-amino)carbonyl)benzenesulfonamide (Duke et al., 1991). Devine and Born (1985) and Peterson and
  Photolytic. The reported photolysis half-lives of chlorsulfuron in distilled water, methanol and natural creek water at λ >290 nm were 18, 92 and 18 hours, respectively. In all cases, 2-chlorobenzene sulfonamide, 2-methoxy-4-methyl-6-amino-1,3,5-triazine and trace amounts of the tentatively identified compound nitroso-2-chlorophenylsulfone formed as photoproducts (Herrmann et al., 1985).

• 代謝経路

  Chlorsulfuron is metabolized in wheat and in tolerant broadleaves via different pathways where hydroxylation occurs on the methyl group of the triazine ring and at the phenyl ring of the chlorsulfuron in respective plants. With chemical degradation of chlorsulfuron on dry minerals (Syst.), two pathways of degradation are observed, one of which is direct

• 輸送方法

  UN3077 Environmentally hazardous substances, solid, n.o.s., Hazard class: 9; Labels: 9-Miscellaneous hazardous material, Technical Name Required.

• 不和合性

  Slowly hydrolyzes in water, releasing ammonia and forming acetate salts. May bencompatible with oxidizers (chlorates, nitrates, peroxides, permanganates, perchlorates, chlorine, bromine, fluorine, etc.); contact may cause fires or explosions. Keep away from alkaline materials, strong bases, strong acids, oxoacids, epoxides.

• 廃棄物の処理

  It is the responsibility of chemical waste generators to determine the toxicity and physical properties and of a discarded chemical and to properly identify its classification and certification as a hazardous waste and to determine the disposal method. United States Environmental Protection Agency guidelines for the classification determination are listed in 40 CFR Parts 261.3. In addition, waste generators must consult and follow all regional, national, state, and local hazardous waste laws to ensure complete and accurate classification and disposal methods. Recycle any unused portion of the material for its approved use or return it to the manufacturer or supplier. Ultimate disposal of the chemical must consider: the material’s impact on air quality; potential migration in soil or water; effects on animal, aquatic, and plant life; and conformance with environmental and public health regulations

1-[(o-クロロフェニル)スルホニル]-3-(4-メトキシ-6-メチル-1,3,5-トリアジン-2-イル)尿素 上流と下流の製品情報

64902-72-3, 1-[(o-クロロフェニル)スルホニル]-3-(4-メトキシ-6-メチル-1,3,5-トリアジン-2-イル)尿素 キーワード