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mesitylene

均三甲苯; 均三甲苯

The Collaborative International Dictionary of English v.0.48 (gcide)

Mesitylene \Me*sit"y*lene\, n. (Chem.)
A colorless, fragrant liquid, {C6H3(CH3)3}, of the benzene
series of hydrocarbons, obtained by distilling acetone with
sulphuric acid. -- {Me*sit`y*len"ic}, a.
[1913 Webster]

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Mesitylene - Wikipedia
Mesitylene is a colorless liquid with sweet aromatic odor It is a component of coal tar , which is its traditional source It is a precursor to diverse fine chemicals
mesitylene - 108-67-8, C9H12, density, melting point, boiling . . .
mesitylene - cas 108-67-8, synthesis, structure, density, melting point, boiling point
Mesitylene | C9H12 | CID 7947 - PubChem
Mesitylene | C9H12 | CID 7947 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety hazards toxicity information, supplier lists, and more
Mesitylene 98 108-67-8 - MilliporeSigma
Mesitylene, also known as 1,3,5-trimethylbenzene, is a benzene derivative Its carbon-13 spin-lattice relaxation times, dipolar relaxation rates and nuclear Overhauser enhancements have been measured to analyze the internal methyl rotation and intermolecular interactions
Mesitylene | 108-67-8 - ChemicalBook
Mesitylene (CAS 108-67-8) information, including chemical properties, structure, melting point, boiling point, density, formula, molecular weight, uses, prices, suppliers, SDS and more, available at Chemicalbook
Mesitylene - chemeurope. com
In organic chemistry, mesitylene or 1,3,5-trimethylbenzene (C 9 H 12) is an aromatic hydrocarbon with three methyl substituents attached to the benzene ring It is prepared from distillation of acetone with sulfuric acid or by the trimerization of propyne in sulfuric acid , which in both cases acts as a homogeneous catalyst and dehydrating agent
Mesitylene - an overview | ScienceDirect Topics
Mesitylene is a type of solvent that, compared to other solvents like decane and dodecane, acts as an H2 acceptor instead of an H2 donor, showing higher activity for the DO reaction due to its unsaturated nature

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