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・ 1,3-Benzodioxolylbutanamine
・ 1,3-beta-D-glucan phosphorylase
・ 1,3-beta-galactosyl-N-acetylhexosamine phosphorylase
・ 1,3-Beta-glucan synthase
・ 1,3-beta-oligoglucan phosphorylase
・ 1,3-Bis(dicyanomethylene)squarate
・ 1,3-Bis(diphenylphosphino)propane
・ 1,3-Bisphosphoglyceric acid
・ 1,3-Butadiene
・ 1,3-Butadiene (data page)
・ 1,3-Butanediol
・ 1,3-Cycloheptadiene
・ 1,3-Cyclohexadiene
・ 1,3-DCP
・ 1,3-Dehydroadamantane
1,3-Diaminopropane
・ 1,3-Diazepine
・ 1,3-Dibromopropane
・ 1,3-Dichlorobenzene
・ 1,3-Dichloropropane
・ 1,3-Dichloropropene
・ 1,3-Difluoro-2-propanol
・ 1,3-Dihydroxyanthraquinone
・ 1,3-Diisocyanatobenzene
・ 1,3-Dimethyl-2-imidazolidinone
・ 1,3-Dimethylbutylamine
・ 1,3-Dioxane
・ 1,3-Dioxetane
・ 1,3-Dioxetanedione
・ 1,3-Dipolar cycloaddition


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1,3-Diaminopropane : ウィキペディア英語版
1,3-Diaminopropane

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1,3-Diaminopropane, also known as , is a simple diamine with the formula (CH2)3(NH2)2. A colourless liquid with a fishy odor, it is soluble in water and many polar organic solvents. It is isomeric with 1,2-diaminopropane. Both are building blocks in the synthesis of heterocycles, such as those used in textile finishing, and coordination complexes. It is prepared by the amination of acrylonitrile followed by hydrogenation of the resulting aminopropionitrile.〔Karsten Eller, Erhard Henkes, Roland Rossbacher, Hartmut Höke "Amines, Aliphatic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. 〕
The potassium salt was used in the alkyne zipper reaction.
== Safety==
Diamines are typically skin irritants.

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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