Names | |
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IUPAC name
2-Methyl-5-(1-methylethenyl)-2-cyclohexen-1-ol
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Systematic IUPAC name
2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-en-1-ol
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Other names
Mentha-6,8-dien-2-ol
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Identifiers | |
3D model (Jmol)
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3DMet | B04241 |
1861032 | |
ChEBI | |
ChemSpider | |
ECHA InfoCard | 100.002.507 |
EC Number | 202-757-4 |
KEGG | |
MeSH | Carveol |
PubChem CID
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RTECS number | OS8400000 |
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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)
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Xi |
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).
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what is ?) | (|
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.