| |||
| Names | |||
|---|---|---|---|
| IUPAC name 1-isopropyl-4-methylcyclohexane | |||
| Identifiers | |||
| |||
3D model (JSmol) | |||
| ChemSpider | |||
| ECHA InfoCard | 100.002.537 | ||
| EC Number |
| ||
| UNII | |||
| |||
| |||
| Properties | |||
| C10H20 | |||
| Molar mass | 140.270 g·mol−1 | ||
| Appearance | Colorless liquid | ||
| Density | 0.8086 g/cm3 | ||
| Boiling point | 168 °C (334 °F; 441 K) | ||
| Solubility in organic solvents | Soluble | ||
Except where otherwise noted, data are given for materials in theirstandard state (at 25 °C [77 °F], 100 kPa). | |||
p-Menthane is ahydrocarbon with the formula (CH3)2CHC6H10CH3. It is the product of the hydrogenation or hydrogenolysis of variousterpenoids, includingp-cymene,terpinolenes,phellandrene, andlimonene. It is a colorless liquid with a fragrant fennel-like odor. It occurs naturally, especially in exudates ofEucalyptus fruits. The compound is generally encountered as a mixture of thecis andtrans isomers, which have very similar properties. It is mainly used as a precursor to itshydroperoxide, which is used to initiatepolymerizations.[1]
