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・ 2-6-6-4
・ 2-6-6-6
・ 2-6-8-0
・ 2-8-0
・ 2-8-0+0-8-2
・ 2-8-2
・ 2-8-2+2-8-2
・ 2-8-4
・ 2-8-6
・ 2-8-8-0
・ 2-8-8-2
・ 2-8-8-4
・ 2-8-8-8-2
・ 2-8-8-8-4
・ 2-acetolactate mutase
2-Acetyl-1-pyrroline
・ 2-Acetyl-5-methylfuran
・ 2-Acetylaminofluorene
・ 2-Acetylfuran
・ 2-Acetylpyridine
・ 2-Acrylamido-2-methylpropane sulfonic acid
・ 2-acylglycerol O-acyltransferase
・ 2-acylglycerol-3-phosphate O-acyltransferase
・ 2-acylglycerophosphocholine O-acyltransferase
・ 2-alkenal reductase
・ 2-alkyn-1-ol dehydrogenase
・ 2-Amino-1,2-dihydronaphthalene
・ 2-Amino-1-methyl-6-phenylimidazo(4,5-b)pyridine
・ 2-amino-3,7-dideoxy-D-threo-hept-6-ulosonate synthase
・ 2-Amino-3-carboxymuconic semialdehyde


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2-Acetyl-1-pyrroline : ウィキペディア英語版
2-Acetyl-1-pyrroline

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2-Acetyl-1-pyrroline, abbreviated 2AP, with the IUPAC name 1-(3,4-dihydro-2''H''-pyrrol-5-yl)ethanone, is an aroma compound and flavor that gives white bread, jasmine rice and basmati rice, the spice ''pandan'' (''Pandanus amaryllifolius''), and ''bread flowers'' (''Vallaris glabra'') their customary smell. 2-Acetyl-1-pyrroline and its structural homolog, 6-acetyl-2,3,4,5-tetrahydropyridine of similar smell, can be formed by Maillard reactions during heating of food such as the baking of bread dough. Both compounds have odor thresholds below 0.06 ng/l.
== Structure and properties ==
2-Acetyl-1-pyrroline is a substituted pyrroline and a cyclic imine as well as a ketone.

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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