Chemistry name: | cymol; isopropyltoluene; methylpropylbenzene |
CAS: | 535-77-3 |
CAS: | 527-84-4 |
CAS: | 99-87-6 |
CAS: | 25155-15 |
M Formula: | CH3C6H4CH(CH3)2 |
Properties: | |
Colorless, transparent liquids with aromatic odor. Combustible. D: o- 0.8748, m- 0.862, p- 0.8551. Fp: o- −71C, m- −64C, p- −68C. Bp:o- 177C, m- 175.6C, p- 176.5C. Refr index: p- 1.489 (20C). Soluble in alcohol, ether, and chloroform; insoluble in water. Flash p (p-) 127F (51C) (CC). | |
Derivation: | |
Mixed cymenes are produced from toluene by alkylation. p-Cymene occurs in several essential oils and is made from monocyclic terpenes by dehydrogenation. These terpenes can be made from turpentine or obtained as a by-product from the sulfite digestion of spruce pulp in paper manufacture. | |
Method of purification: | |
Washing with sulfuric acid, water, and alkali. | |
Grade: | |
Technical. | |
Hazard: | |
Moderate fire risk. Moderately toxic by ingestion. | |
Use: | |
Solvents, synthetic-resin manufacture, metal polishes, organic synthesis (oxidation to hydroperoxides used as catalysts for synthetic-rubber manufacture; cymene alcohols are made by hydrogenating the hydroperoxides). Pure p-cresol and carvacrol are made from p-cymene. | |
The o-, m-, and p-isomers are known.