| Names | |
|---|---|
|
IUPAC name
2-Methyl-5-(1-methylethenyl)-2-cyclohexen-1-ol
|
|
|
Systematic IUPAC name
2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-ol
|
|
| Other names
Mentha-6,8-dien-2-ol
|
|
| Identifiers | |
|
3D model (Jmol)
|
|
| 3DMet | B04241 |
| 1861032 | |
| ChEBI | |
| ChemSpider | |
| ECHA InfoCard | 100.002.507 |
| EC Number | 202-757-4 |
| KEGG | |
| MeSH | Carveol |
|
PubChem CID
|
|
| RTECS number | OS8400000 |
|
|
|
|
| Properties | |
| C10H16O | |
| Molar mass | 152.24 g·mol−1 |
| Density | 0.958 g cm−3 |
| Boiling point | 226 to 227 °C (439 to 441 °F; 499 to 500 K) |
| Hazards | |
|
EU classification (DSD)
|
|
| R-phrases | R36/37/38 |
| S-phrases | S26 S37/39 |
| NFPA 704 | |
| Flash point | 98 °C (208 °F; 371 K) |
|
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
|
|
|
|
| Infobox references | |
Carveol is a natural unsaturated, monocyclic monoterpenoid alcohol that is a constituent of spearmint essential oil in the form of cis-(−)-carveol. It is a colorless fluid soluble in oils, but insoluble in water and has an odor and flavor that resemble those of spearmint and caraway. Consequently, it is used as a fragrance in cosmetics and as a flavor additive in the food industry.
It has been found to exhibit chemoprevention of mammary carcinogenesis (prevents breast cancer).
An alpha-trans-dihydroxy derivative ((1R,2R,6S)-3-methyl-6-(prop-1-en-2-yl)cyclohex-3-ene-1,2-diol) possesses potent antiparkinsonian activity in animal models.