翻訳と辞書
Words near each other
・ 1,1-Ethanedithiol
・ 1,2,3 Soleils
・ 1,2,3,4,6-Pentagalloyl glucose
・ 1,2,3,4-Tetraphenylnaphthalene
・ 1,2,3,5-Tetrahydroxybenzene
・ 1,2,3-Triazole
・ 1,2,3-Tribromopropane
・ 1,2,3-Trichloropropane
・ 1,2,3-Trimethylbenzene
・ 1,2,3-Trinitrobenzene
・ 1,2,4-Butanetriol
・ 1,2,4-Butanetriol trinitrate
・ 1,2,4-Triazole
・ 1,2,4-Trichlorobenzene
・ 1,2,4-Trihydroxyanthraquinone
1,2,4-Trimethylbenzene
・ 1,2,4-Trioxane
・ 1,2,6-Trigalloyl glucose
・ 1,2-alpha-L-fucosidase
・ 1,2-alpha-mannosidase
・ 1,2-Benzenedithiol
・ 1,2-Benzoquinone
・ 1,2-Bis(dicyanomethylene)squarate
・ 1,2-Bis(diisopropylphosphino)ethane
・ 1,2-Bis(dimethylarsino)benzene
・ 1,2-Bis(dimethylphosphino)ethane
・ 1,2-Bis(diphenylphosphino)ethane
・ 1,2-Butanediol
・ 1,2-Butylene carbonate
・ 1,2-Cyclohexane dicarboxylic acid diisononyl ester


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1,2,4-Trimethylbenzene : ウィキペディア英語版
1,2,4-Trimethylbenzene

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1,2,4-Trimethylbenzene is an organic compound with the chemical formula C6H3(CH3)3. Classified as an aromatic hydrocarbon, it is a flammable colorless liquid with a strong odor. It is nearly insoluble in water but soluble in organic solvents. It occurs naturally in coal tar and petroleum (about 3%).
==Production==
Industrially, it is isolated from the C9 aromatic hydrocarbon fraction during petroleum distillation. Approximately 40% of this fraction is 1,2,4-trimethylbenzene. It is also generated by methylation of toluene and xylenes and the disproportionation of xylene over aluminosilicate catalysts.〔Karl Griesbaum, Arno Behr, Dieter Biedenkapp, Heinz-Werner Voges, Dorothea Garbe, Christian Paetz, Gerd Collin, Dieter Mayer, Hartmut Höke "Hydrocarbons" in Ullmann's Encyclopedia of Industrial Chemistry 2002 Wiley-VCH, Weinheim. 〕

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「1,2,4-Trimethylbenzene」の詳細全文を読む



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