4-ブチルフェノール 化学特性,用途語,生産方法
外観
うすい黄色～褐色, 澄明の液体
溶解性
エタノール、アセトン及びヘキサンに溶け、水に溶けにくい。ヘキサンに溶ける
用途
環境試料中の内分泌攪乱物質の分析(HPLC)用標準品、GC-MS分析標準品。
使用上の注意
不活性ガス封入
化学的特性
liquid
使用
Intermediates of Liquid Crystals
安全性プロファイル
A poison. Questionable
carcinogen with experimental tumorigenic v v
data. When heated to decomposition it
emits acrid smoke and irritating fumes. See
also PHENOL and other butyl phenols.
職業ばく露
Butylphenols may be used as intermediates in manufacturing varnish and lacquer resins; as a
germicidal agent in detergent disinfectants; as a pour point
depressant, in motor-oil additives; de-emulsifier for oil;
soap-antioxidant, plasticizer, fumigant, and insecticide
輸送方法
UN2430 Alkylphenols, solid, n.o.s. (including
C2-C12 homologues), Hazard class: 8; Labels: 8—
Corrosive material
不和合性
Vapors may form explosive mixture with
air. These phenol/cresol materials can react with oxidizers;
reaction may be violent. Incompatible with strong reducing
substances such as hydrides, nitrides, alkali metals, and sulfides. Flammable gas (H2) is often generated, and the heat
of the reaction may cause the gas to ignite and explode.
Heat is also generated by the acid-base reaction with bases;
such heating may initiate polymerization of the organic
compound. React with boranes, alkalies, aliphatic amines,
amides, nitric acid, sulfuric acid. Phenols are sulfonated
very readily (for example, by concentrated sulfuric acid at
room temperature). These reactions generate heat. Phenols
are also nitrated very rapidly, even by dilute nitric acid and
can explode when heated. Many phenols form metal salts
that may be detonated by mild shock
4-ブチルフェノール 上流と下流の製品情報
原材料
準備製品