翻訳と辞書 ・ 1,4-Naphthoquinone
・ 1,4-Thiazepine
・ 1,5-anhydro-D-fructose dehydratase
・ 1,5-anhydro-D-fructose reductase
・ 1,5-anhydro-D-fructose reductase (1,5-anhydro-D-mannitol-forming)
・ 1,5-Anhydroglucitol
・ 1,5-Cyclooctadiene
・ 1,5-Diazabicyclo(4.3.0)non-5-ene
・ 1,5-Dihydroxynaphthalene
・ 1,5-Methano(10)annulene
・ 1,5-Pentanediol
・ 1,6-alpha-D-mannosidase
・ 1,6-alpha-L-fucosidase
・ 1,6-Digalloyl glucose
・ 1,6-dihydroxycyclohexa-2,4-diene-1-carboxylate dehydrogenase
・ 1,6-Hexanediol
・ 1,6-Methano(10)annulene
・ 1,68
・ 1,7-Bis(4-hydroxyphenyl)-1,4,6-heptatrien-3-one
・ 1,778 Stories of Me and My Wife
・ 1,8-Bis(dimethylamino)naphthalene
・ 1,8-Cineole 2-endo-monooxygenase
・ 1,8-Cineole 2-exo-monooxygenase
・ 1,8-cineole synthase
・ 1,8-Diaminonaphthalene
・ 1,8-Diazabicycloundec-7-ene
・ 1,8-Diazafluoren-9-one
・ 1,8-Octanediol
・ 1,837 Seconds of Humor
・ 1,9-Pyrazoloanthrone
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| 1,6-Hexanediol ： ウィキペディア英語版 |
1,6-Hexanediol
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1,6-Hexanediol (HOCH2(CH2)4CH2OH) is a colorless crystalline solid that melts at 42 °C and boils at 250 °C.〔 It is soluble in water and is hygroscopic.
== Production ==
1,6-Hexanediol is prepared industrially by the hydrogenation of adipic acid. Laboratory synthesis can be done by reduction of adipic acid with lithium aluminium hydride, however, since it is cheaply and commercially available, it is usually not synthesized in the laboratory.
抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』
■ウィキペディアで「1,6-Hexanediol」の詳細全文を読む
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