1-(4-クロロフェノキシ)-1-(1H-1,2,4-トリアゾール-1-イル)-3,3-ジメチルブタン-2-オン

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

  H302：飲み込むと有害

  H317：アレルギー性皮膚反応を起こすおそれ

  H330：吸入すると生命に危険

  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。

  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。

  P301+P312：飲み込んだ場合：気分が悪い時は医師に連絡する こと。

  P302+P352：皮膚に付着した場合：多量の水と石鹸で洗うこと。

1-(4-クロロフェノキシ)-1-(1H-1,2,4-トリアゾール-1-イル)-3,3-ジメチルブタン-2-オン 価格

MSDS Information

• 1-(tert-Butylcarbonyl-(4-chlorophenoxy)methyl)-1H-1,2,4-triazole

1-(4-クロロフェノキシ)-1-(1H-1,2,4-トリアゾール-1-イル)-3,3-ジメチルブタン-2-オン 化学特性,用途語,生産方法

• 外観

  白色～わずかにうすい黄色, 結晶性粉末

• 溶解性

  水64mg/l(20℃)。多くの有機溶媒に溶ける。ジクロロメタン, トルエン＞200,イソプロパノール50～100, ヘキサン5～10(全てg/l 20℃)。

• 用途

  DMI剤（脱メチル化阻害剤）茎葉処理剤や種子処理剤として使用

• 農薬用途

  殺菌剤

• 説明

  Triadimefon has been a widely used fungicide on crops and nonfood products since the early 1970s. The metabolite triadimenol is also active and is registered separately for use as seed treatment. Triadimenol has a broad regulatory toxicology database, but its toxicity is considered to be encompassed in that of triadimefon and therefore the same study was used by the United States Environmental Protection Agency (US EPA) in establishing regulatory levels for both pesticides. In nontarget species, dopaminergic neurotoxicity is the primary effect, but with chronic exposures its toxicities include hepatic, carcinogenic, developmental, and reproductive effects.

• 使用

  Triadimefon is an triazole fungicide is used for the management of mango powdery mildew in South Gujarat.

• 一般的な説明

  Colorless to pale yellow crystalline solid with a slight odor.

• 空気と水の反応

  Insoluble in water.

• 反応プロフィール

  Triadimefon is incompatible with strong oxidizing agents and acids. Reacts with acid halides and anhydrides. Also reacts with most active hydrogen compounds .

• 火災危険

  Flash point data for Triadimefon are not available; however, Triadimefon is probably combustible.

• 作用机制

  C14位脱メチル化酵素を阻害することによって効果を発揮する

• 农业用途

  Fungicide: Triadimefon is a systemic fungicide that is used to control powdery mildews, rusts, and other fungi on coffee, seed grasses, cereals, fruits, grapes, vegetables, vines, pineapple, sugar cane, sugar beets, turf, shrubs, and trees. Not approved for use in EU countries. Registered for use in the U.S. U.S. Maximum Allowable Residue Levels for Triadimefon

• 製品名

  ACCOST®; ACIZOL®; AMIRAL®; BAY® 6681-F; BAYLETON®; BAY®-MEB-6447; BAYER® 6681-F; BAYER® MEB-6447; MEB 6447®; PRO-TEK®; ROFON®

• 薬理学

  Triadimefon (36) and its alcohol analog triadimenol (37) have been intensively investigated to determine the influence of their enantiomeric difference on fungicidal activity. Between stereoisomeric triadimefon, no significant difference is observed in their fungicidal activity. However, triadimenol, which shows a much higher fungicidal activity than triadimefon, exhibits a clear stereochemistry-dependent activity difference. Greater fungicidal activity is possessed by the (1S, 2R)-isomer (28).

• 安全性プロファイル

  Poison by ingestion. Mutation data reported. When heated to decomposition it emits very toxic fumes of Cland NOx. See also KETONES.

• 環境運命予測

  Soil. In a culture study, the microorganism Aspergillus niger degraded 32% of tri- adimefon to triadimenol after 5 days (Clark et al., 1978).
  Plant. In soils and plants, triadimefon degrades to triadimenol (Clark et al., 1978; Rouchaud et al., 1981). In barley plants, triadimefon was metabolized to triadimenol and p-chlorophenol (Rouchaud et al., 1981; Rouchaud, 1982). In the grains an
  Photolytic. When triadimefon was subjected to UV light for one week, p-chlorophenol, 4-chlorophenyl methyl carbamate and a 1,2,4-triazole formed as products (Clark et al., 1978).

• 代謝経路

  Enzymic reduction of triadimefon is an important pathway in plants, soils and fungi and may be regarded as an activation process, which produces fungicidally active triadimenol. Two diastereoisomers of triadimenol, A and B [( 1RS,2SR)-l-(4-chlorophenoxy)-3,3-dimethyl^-1-(1H-1,2,4-triazol^-1-yl) butan-2-ol is referred to as diastereoisomer A; 1RS,2RS- is referred to as diastereoisomer β], are produced in different amounts by plants and fungi and the proportions may differ within the plant. Similar metabolic pathways are followed in mammals where reduction of the keto group yields triadimenol as the principal metabolite and oxidation of the butyl group gives alcohol and carboxylic acid derivatives.

1-(4-クロロフェノキシ)-1-(1H-1,2,4-トリアゾール-1-イル)-3,3-ジメチルブタン-2-オン 上流と下流の製品情報

1-(4-クロロフェノキシ)-1-(1H-1,2,4-トリアゾール-1-イル)-3,3-ジメチルブタン-2-オン 生産企業

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