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・ N-Hydroxysuccinimide
・ N-hydroxythioamide S-beta-glucosyltransferase
・ N-I (rocket)
・ N-II (rocket)
・ N-isopropylammelide isopropylaminohydrolase
・ N-jet
・ N-Joi
・ N-JOY
・ N-Joy
・ N-Joypad
・ N-linked glycosylation
・ N-localizer
・ N-malonylurea hydrolase
・ N-methyl nucleosidase
・ N-methyl-2-oxoglutaramate hydrolase
N-Methyl-2-pyrrolidone
・ N-Methyl-3-piperidyl benzilate
・ N-Methyl-D-aspartic acid
・ N-methyl-L-amino-acid oxidase
・ N-Methyl-L-glutamic acid
・ N-Methyl-N-ethyltryptamine
・ N-Methyl-PPPA
・ N-methylalanine dehydrogenase
・ N-Methylaniline
・ N-Methylcarfentanil
・ N-methylcoclaurine 3'-monooxygenase
・ N-Methylconiine
・ N-Methylephedrine
・ N-Methylethanolamine
・ N-Methylformamide


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N-Methyl-2-pyrrolidone : ウィキペディア英語版
N-Methyl-2-pyrrolidone

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''N''-Methyl-2-pyrrolidone (NMP) is an organic compound consisting of a 5-membered lactam. It is a colorless liquid, although impure samples can appear yellow. It is miscible with water and with most common organic solvents. It also belongs to the class of dipolar aprotic solvents such as dimethylformamide and dimethyl sulfoxide. It is used in the petrochemical and plastics industries as a solvent, exploiting its nonvolatility and ability to dissolve diverse materials.〔Albrecht Ludwig Harreus, R. Backes, J.-O. Eichler, R. Feuerhake, C. Jäkel, U. Mahn, R. Pinkos, R. Vogelsang"2-Pyrrolidone" in ''Ullmann's Encyclopedia of Industrial Chemistry'', Wiley-VCH, 2011, Weinheim. 〕
==Preparation==
NMP is produced industrially by a typical ester-to-amide conversion, by treating butyrolactone with methylamine. Alternative routes include the partial hydrogenation of ''N''-methylsuccinimide and the reaction of acrylonitrile with methylamine followed by hydrolysis. About 20,000 to 30,000 tons are produced annually.〔

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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