ジアミルアミン

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

  H226：引火性の液体および蒸気

  H314：重篤な皮膚の薬傷?眼の損傷

• 注意書き

  P210：熱/火花/裸火/高温のもののような着火源から遠ざ けること。－禁煙。

  P233：容器を密閉しておくこと。

  P240：容器を接地すること/アースをとること。

  P241：防爆型の電気機器/換気装置/照明機器/．．．機器を使 用すること。

  P242：火花を発生させない工具を使用すること。

  P243：静電気放電に対する予防措置を講ずること。

  P264：取扱い後は皮膚をよく洗うこと。

  P264：取扱い後は手や顔をよく洗うこと。

  P270：この製品を使用する時に、飲食または喫煙をしないこ と。

  P280：保護手袋/保護衣/保護眼鏡/保護面を着用するこ と。

  P301+P330+P331：飲み込んだ場合：口をすすぐこと。無理に吐かせ ないこと。

  P303+P361+P353：皮膚（または髪）に付着した場合：直ちに汚染された衣 類をすべて脱ぐこと/取り除くこと。皮膚を流水/シャワー で洗うこと。

  P370+P378：火災の場合：消火に．．．を使用すること。

  P403+P235：換気の良い場所で保管すること。涼しいところに 置くこと。

  P405：施錠して保管すること。

  P501：内容物/容器を．．．に廃棄すること。

ジアミルアミン 価格

MSDS Information

• N-Pentyl-1-pentanamine

ジアミルアミン 化学特性,用途語,生産方法

• 外観

  無色～黄褐色, 澄明の液体

• 溶解性

  水に不溶。エタノールに混和。

• 用途

  有機合成原料。

• 化学的特性

  Diamylamine is a relatively strong base and forms salts with acids. Its vapors can form explosive mixtures with air.

• 使用

  Di-n-amylamine is manufactured from amyl chloride and ammonia. It is used in organic syntheses and as a solvent, rubber accelerator, flotation reagent, and corrosion inhibitor.

• 調製方法

  Diamylamine is manufactured by the same processes as n-amylamine by reaction of amyl chloride with ammonia and then separated from the amylenes and amyl alcohol by steam distillation (Hawley 1977). It also can be synthesized by amination of alkyl halides at high temperature and pressure (Schweizer et al 1978). The commercial product may be a mixture of amyl isomers (HSDB 1989).

• 一般的な説明

  A clear colorless liquid with an ammonia-like odor. Very slightly soluble in water. Density 6.40 lb / gal (less than water) Vapors heavier than air. Flash point 152°F. Difficult to ignite. Moderately toxic. Contact with liquid may cause a chemical burn. Vapors may irritate respiratory tract. Used in the manufacture of rubber, resins, and dyes.

• 空気と水の反応

  Flammable. Sensitive to air and heat. Slightly soluble in water.

• 反応プロフィール

  Diamylamine neutralizes acids to form salts plus water. May be incompatible with isocyanates, halogenated organics, peroxides, phenols (acidic), epoxides, anhydrides, and acid halides. Flammable gaseous hydrogen is generated in combination with strong reducing agents, such as hydrides.

• 健康ハザード

  Diamylamine is a strong eye, skin, and respiratory irritant owing to its basicity (HSDB 1989). Vapor exposure results in irritation of the nose and throat with distressed breathing and coughing. Prolonged exposure may lead to pulmonary edema. Direct skin contact can cause secondary burns.

• 火災危険

  HIGHLY FLAMMABLE: Will be easily ignited by heat, sparks or flames. Vapors may form explosive mixtures with air. Vapors may travel to source of ignition and flash back. Most vapors are heavier than air. They will spread along ground and collect in low or confined areas (sewers, basements, tanks). Vapor explosion and poison hazard indoors, outdoors or in sewers. Runoff to sewer may create fire or explosion hazard. Containers may explode when heated. Many liquids are lighter than water.

• 工業用途

  Diamylamine is less widely used than n-amylamine with only 20 tons being manufactured in the U.S. in 1976. Its most widespread use is as a corrosion inhibitor and rubber accelerator (Hawley 1977). It is also useful as a solvent for oils, resins, and some cellulose esters. Introduction of the amyl group imparts oil solubility to otherwise oil-insoluble substances. Diamylamine also is used in flotation reagents, dyestuffs and as a cockroach repellent (HSDB 1989).

• 安全性プロファイル

  Poison by inhalation, ingestion, and skin contact. A severe skin irritant. See also AMINES. Flammable liquid when exposed to heat or flame; can react with oxidizing materials. To fight fire, use alcohol foam, foam, CO2, dry chemical. When heated to decomposition it emits toxic fumes of NOx.

• 代謝

  In contrast to n-amylamine, little information is available on diamylamine metabolism, particularly with respect to its suitability as a substrate for the amine oxidases. Generally, the rate of oxidation of secondary amines by monoamine oxidase is slower than that of primary amines (Beard and Noe 1981). In agreement, Yamada et al (1965) demonstrated that crystalline amine oxidase prepared from Aspergillus niger oxidized diamylamine very slowly with respect to n-amylamine.
  As with other secondary aliphatic amines, the propensity of diamylamine to form nitrosamines is of interest. It has been shown that treatment of diamylamine with nitrous acid in dilute aqueous solution gave optimum nitrosamine formation between pH 1 and 3, corresponding to stomach conditions (Sander et al 1968). When rats were fed a diet supplemented with sodium nitrite and secondary amines of low basicity, synthesis of nitrosamines in the stomach was observed. Malignant tumors arising through formation of nitrosamines in the stomach was demonstrated only when nitrite was present in the stomach concomitantly with secondary amines which readily formed carcinogenic nitrosamines.

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ジアミルアミン スペクトルデータ(¹HNMR、¹³CNMR、IR1、MS、Raman)

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