甲苯 - 百度百科
1844年甲苯由法国科学家 HenriEtienne Sainte-Claire Deville 通过对吐鲁香胶的干馏首次制备成功，甲苯的英语名称 toluene 也由此而来。 1861年，德国化学家约瑟夫·威尔布兰特用甲苯作原料，首次合成了不纯的 TNT 。
甲苯 - 维基百科，自由的百科全书
甲苯（英語： Toluene ）是一种无色带特殊芳香味的易挥发 液体，分子式為C 7 H 8 ，難溶於水。
Toluene - Wikipedia
Toluene is irritating to the eyes, skin, and respiratory tract. It is absorbed slowly through the skin. It can cause systemic toxicity by inhalation or ingestion.
FRIEDEL-CRAFTS REACTIONS OF BENZENE AND METHYLBENZENE …
This page gives details of the Friedel-Crafts reactions of benzene and methylbenzene (toluene). The mechanisms for some of these reactions are covered elsewhere on the site and you will find links to those as you go along.
Toluene | C6H5CH3 | CID 1140 - PubChem
Purified toluene contains about 0.01% benzene, but crude toluene may contain as much as 25% benzene. Rotogravure printers were exposed to high concentrations of toluene (decreasing from about 1710 ppm in 1969 to about 43-157 ppm in 1980).
甲苯 - 維基百科，自由的百科全書
Toluene and xylene are preferred IUPAC names, but are not freely substitutable; toluene is substitutable under certain conditions, but only for general nomenclature (see P-15.1.8 for a general substitution rules for retained names).
Halogenation of Benzene and Methylbenzene - Chemistry …
2023年1月23日 · This page looks at the reactions of benzene and methylbenzene (toluene) with chlorine and bromine under various conditions. The halogenation of benzene Substitution reactions
Toluene - Thermophysical Properties - The Engineering ToolBox
2012年11月4日 · Chemical, physical and thermal properties of toluene, also called methylbenzene, toluol and phenylmethane. Phase diagram included. Toluene, C 6 H 5 -CH 3 , is a clear colorless liquid, highly flammable with a sweet, pungent aromatic odor.
Toluene - Chemical Safety Facts
2022年10月14日 · Toluene, also known as methylbenzene, is a clear, colorless liquid with a distinctive sweet smell that is widely used in industrial settings as a solvent.
HALOGENATION OF BENZENE AND METHYLBENZENE
This page looks at the reactions of benzene and methylbenzene (toluene) with chlorine and bromine under various conditions. The mechanisms for several of these reactions are covered elsewhere on the site and you will find links to these other pages.
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