1-ヘプタノール 化学特性,用途語,生産方法
外観
無色澄明の液体
溶解性
エタノール及びアセトンに溶けやすく、水に極めて溶けにくい。
解説
C7H16O(116.20).CH3(CH2)5CH2OH.1-ヘプタノールともいう.炭素数7の脂肪族飽和アルコールで,直鎖状,末端炭素にヒドロキシ基をもつものをいう.工業的には,エテンをチーグラー触媒で三量化してヘキセンとし,これをオキソ合成でヘプチルアルコール(異性体混合物)に変換すると得られる.無色の液体.融点-34.0 ℃,沸点176.2 ℃.d254 0.8191.n25D 1.4223.エタノール,エーテルに可溶,水に微溶.ヘプチルアルコールは,ソフト型合成洗剤,界面活性剤,可塑剤,医薬品,化粧品などの合成原料として用いられる.森北出版「化学辞典(第2版)
用途
有機合成原料、溶剤。
用途
化粧品用溶剤、有機合成用溶剤にもちいられるほか、カーネーションやジャスミンの花の香りなどにも使われる。
説明
Heptyl alcohol has a faint, aromatic, fatty odor and a pungent,
spicy taste. It may be synthesized by reduction of enanthic aldehyde, which is a distillation product of castor oil.
化学的特性
colourless liquid
天然物の起源
Reported found in a few essential oils, hyacinth, violet leaves, Litsea zeylanica Also reported found in apple, banana, citrus peel oils, orange juice, bilberry, cranberry, blueberry, other berries, currants, melon, papaya, peach, pear, pineapple, asparagus, peas, potato, mustard, cheeses, butter, milk, meats, hop oil, beer, cognac, rum, bourbon whiskey, grape wines, cocoa, tea, flberts, pecans, peanuts, soybeans, passion fruit juice, olive, macadamia nuts, mango, tamarind, fgs, cardamom, rice, calamus, dill, corn, malt, kiwifruit, truffe, nectarine, crab, crayfsh, clams and other sources
使用
1-Heptanol have also been used in the fragrance industry due to its pleasant smell.
製造方法
By reduction of enanthic aldehyde, which is a distillation product of castor oil.
調製方法
1-Heptanol is produced by reacting hexenes with carbon
monoxide in the oxo process or by the catalytic reduction
of heptaldehyde. It has little commercial value except in
fragrances and as an artificial flavoring agent.
一般的な説明
Colorless oily liquid. 0.2% soluble in water,
soluble in alcohol, miscible with oils.
Sp.Gr. 0.82. B.P. 175° C.
Fresh and light, green-fatty, winey and saPIike odor of poor tenacity.
Sweet winey-nut-like taste. Green only in
high concentration.
反応プロフィール
Heptan-1-ol is an alcohol. Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides.
危険性
Combustible.
健康ハザード
Low toxicity; liquid may irritate eyes.
化学反応性
Reactivity with Water No reaction; Reactivity with Common Materials: No reactions; Stability During Transport: Stable; Neutralizing Agents for Acids and Caustics: Not pertinent; Polymerization: Not pertinent; Inhibitor of Polymerization: Not pertinent.
純化方法
Shake the alcohol with successive lots of alkaline KMnO4 until the colour persists for 15minutes, then dry it with K2CO3 or CaO, and fractionally distil it. [Beilstein 1 IV 1731.]
1-ヘプタノール 上流と下流の製品情報
原材料
準備製品