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・ Propionate CoA-transferase
・ Propionate kinase
・ Propionate—CoA ligase
・ Propionibacteriaceae
・ Propionibacterineae
・ Propionibacterium
・ Propionibacterium acnes
・ Propionibacterium freudenreichii
・ Propionibacterium propionicus
・ Propionibacterium zappae
・ Propionic acid
・ Propionic acidemia
・ Propionic anhydride
・ Propionigenium modestum
・ Propionispora
Propionitrile
・ Propionivibrio
・ Propionivibrio dicarboxylicus
・ Propionivibrio limicola
・ Propionivibrio pelophilus
・ Propionycha
・ Propionyl coenzyme A carboxylase
・ Propionyl-CoA
・ Propionyl-CoA C2-trimethyltridecanoyltransferase
・ Propionyl-CoA carboxylase
・ Propiophenone
・ Propiram
・ Propiromorpha
・ Propiska
・ Propiska in the Soviet Union


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Propionitrile : ウィキペディア英語版
Propionitrile

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Propionitrile, also known as ethyl cyanide and propanenitrile, is an organic compound with the formula CH3CH2CN. It is a simple aliphatic nitrile. The compound is a colourless, water-soluble liquid. It is used as a solvent and a precursor to other organic compounds.〔
==Production==
The main industrial route to this nitrile is the hydrogenation of acrylonitrile. It is also prepared by the ammoxidation of propanol (propionaldehyde can also be used instead):〔Peter Pollak, Gérard Romeder, Ferdinand Hagedorn, Heinz-Peter Gelbke "Nitriles" in Ullmann's Encyclopedia of Industrial Chemistry 2002, Wiley-VCH, Weinheim. 〕
:CH3CH2CH2OH + O2 + NH3 → CH3CH2CN + 3 H2O
Propionitrile is a byproduct of the electrodimerisation of acrylonitrile to adiponitrile.
In the laboratory propanenitrile can also be produced by the dehydration of propionamide, by catalytic reduction of acrylonitrile, or by distilling ethyl sulfate and potassium cyanide.

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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