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・ 4-Methylaminobutanoate oxidase (formaldehyde-forming)
・ 4-Methylaminobutanoate oxidase (methylamine-forming)
・ 4-Methylaminorex
・ 4-Methylamphetamine
・ 4-Methylbenzaldehyde
・ 4-Methylbenzylidene camphor
・ 4-Methylbuphedrone
・ 4-Methylcatechol
・ 4-Methylcathinone
・ 4-Methylcyclohexanemethanol
・ 4-Methyldiphenhydramine
・ 4-methyleneglutamate—ammonia ligase
・ 4-methyleneglutaminase
・ 4-Methylethcathinone
・ 4-Methylhistamine
4-Methylimidazole
・ 4-Methylmethamphetamine
・ 4-Methylmethylphenidate
・ 4-methyloxaloacetate esterase
・ 4-Methylpentanoic acid
・ 4-Methylpentedrone
・ 4-Methylphenethylamine
・ 4-Methylphenylisobutylamine
・ 4-Methylpregabalin
・ 4-Methylpyridine
・ 4-Methylsalicylic acid
・ 4-Methylthioamphetamine
・ 4-millimeter band
・ 4-MMA
・ 4-NEMD


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4-Methylimidazole : ウィキペディア英語版
4-Methylimidazole

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4-Methylimidazole (4-MeI or 4-MEI) is a heterocyclic organic chemical compound with molecular formula – or . It is formally derived from imidazole through replacement of the hydrogen in position 4 by a methyl group. It is a slightly yellowish solid.
4-MeI may be formed in the browning of certain foods through the Maillard reaction between carbohydrates and amino-containing compounds. In particular, it is found in roasted foods, grilled meats, coffee and in types of caramel coloring produced with ammonia-based processes.〔〔http://oehha.ca.gov/public_info/facts/pdf/4MEIfacts_021012.pdf〕 It may arise also by fermentation.
==Preparation and structure==
4-MeI may be prepared using the Debus-Radziszewski imidazole synthesis, by reacting methylglyoxal with ammonia and formaldehyde. It may also be prepared by the reaction of hydroxyacetone and formamide in ammonia.
Small energy difference separates 4-methylimidazole from its tautomer 5-methylimidazole.〔G.-S. Li, M. F. Ruiz-López, B. Maigret "Ab Initio Study of 4(5)-Methylimidazole in Aqueous Solution" J. Phys. Chem. A, 1997, vol. 101, pp 7885–7892. 〕

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