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・ 2-Bromomescaline
・ 2-Bromopropane
・ 2-Butanol
・ 2-Butene
・ 2-Butoxyethanol
・ 2,5-Dimethoxybenzaldehyde
・ 2,5-Dimethylfuran
・ 2,5-Dimethylhexane
・ 2,5-dioxopiperazine hydrolase
・ 2,5-dioxovalerate dehydrogenase
・ 2,5-Diphenyloxazole
・ 2,5-Furandicarboxylic acid
・ 2,5-Xylidine
・ 2,500 year celebration of the Persian Empire
・ 2,6-beta-fructan 6-levanbiohydrolase
2,6-Di-tert-butylphenol
・ 2,6-Di-tert-butylpyridine
・ 2,6-Diacetylpyridine
・ 2,6-Diaminopurine
・ 2,6-Dichlorobenzonitrile
・ 2,6-Dichlorophenol
・ 2,6-Dihydroxybenzoic acid
・ 2,6-dihydroxypseudooxynicotine hydrolase
・ 2,6-Dihydroxypyridine
・ 2,6-dihydroxypyridine 3-monooxygenase
・ 2,6-Dimethoxybenzoquinone
・ 2,6-Dimethylnaphthalene
・ 2,6-Dimethylpiperidine
・ 2,6-dioxo-6-phenylhexa-3-enoate hydrolase
・ 2,6-Lutidine


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2,6-Di-tert-butylphenol : ウィキペディア英語版
2,6-Di-tert-butylphenol

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2,6-Di-''tert''-butylphenol is an organic compound with the structural formula 2,6-((CH3)3C)2C6H3OH. This colorless solid alkylated phenol and its derivatives are used industrially as UV stabilizers and antioxidants for hydrocarbon-based products ranging from petrochemicals to plastics. Illustrative of its usefulness, it prevents gumming in aviation fuels.
==Production==
2,6-Di-''tert''-butylphenol is prepared by the reaction of phenol with isobutene catalyzed by aluminium phenoxide:
〔Helmut Fiege, Heinz-Werner Voges, Toshikazu Hamamoto, Sumio Umemura, Tadao Iwata, Hisaya Miki, Yasuhiro Fujita, Hans-Josef Buysch, Dorothea Garbe, Wilfried Paulus "Phenol Derivatives" in ''Ullmann's Encyclopedia of Industrial Chemistry'', Wiley-VCH, Weinheim, 2002. Article Online Posting Date: June 15, 2000.〕
:C6H5OH + 2 CH2=C(CH3)2 → ((CH3)3C)2C6H3OH
In this way, approximately 2.5M kg/y are produced.

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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