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・ Glycoprotein-N-acetylgalactosamine 3-beta-galactosyltransferase
・ Glycoproteinosis
・ Glycoproteomics
・ Glycopyrronium bromide
・ Glycorandomization
・ Glycosaminoglycan
・ Glycosaminoglycan galactosyltransferase
・ Glycerophospholipid
・ Glycerophospholipid acyltransferase (CoA-dependent)
・ Glycerophospholipid arachidonoyl-transferase (CoA-independent)
・ Glycerophthora
・ Glyceryl behenate
・ Glyceryl hydroxystearate
・ Glycia
・ Glycidic acid
Glycidol
・ Glycidyl methacrylate
・ Glycin
・ Glycine
・ Glycine (data page)
・ Glycine (plant)
・ Glycine betaine aldehyde
・ Glycine C-acetyltransferase
・ Glycine clandestina
・ Glycine cleavage system
・ Glycine dehydrogenase
・ Glycine dehydrogenase (cyanide-forming)
・ Glycine dehydrogenase (cytochrome)
・ Glycine dehydrogenase (decarboxylating)
・ Glycine encephalopathy


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Glycidol : ウィキペディア英語版
Glycidol

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Glycidol is an organic compound that contains both epoxide and alcohol functional groups. Being bifunctional, it has a variety of industrial uses. The compound is a slightly viscous liquid that is slightly unstable and is not often encountered in pure form.
==Synthesis and applications==
Glycidol is prepared by the epoxidation of allyl alcohol.〔Guenter Sienel, Robert Rieth, Kenneth T. Rowbottom "Epoxides" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2005. 〕
Glycidol is used as a stabilizer for natural oils and vinyl polymers and as a demulsifier. It is used as a chemical intermediate in the synthesis of glycerol, glycidyl ethers, esters and amines. It is used in surface coatings, chemical synthesis, pharmaceuticals, sanitary chemicals and sterilizing milk of magnesia, and as a gelation agent in solid propellants.〔(Glycidol at chemicalland21.com )〕

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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