| Weight | 152.237 g/mol |
|---|---|
| Formula | C10H16O |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
CARVEOL (2102-59-2, 99-48-9)
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- Monoterpene Metabolism. Cloning, Expression, and Characterization of ()-Isopiperitenol/()-Carveol Dehydrogenase of Peppermint and Spearmint (Plant Physiology, 2005)
- Biotransformation of d-Limonene to (+) trans-Carveol by Toluene-Grown Rhodococcus opacus PWD4 Cells (Applied and Environmental Microbiology, 2001)
- Improved Reactor Performance and Operability in the Biotransformation of Carveol to Carvone Using a Solid-Liquid Two-Phase Partitioning Bioreactor (Biotechnology and Bioengineering, 2008)
- Maintenance of cell viability in the biotransformation of (-)-carveol with whole cells of Rhodococcus erythropolis (Journal of Molecular Catalysis B-enzymatic, 2002)
- Gas-phase ozonolysis of the monoterpenoids (S)-(+)-carvone, (R)-( )-carvone, ( )-carveol, geraniol and citral (Atmospheric Environment, 2005)
- Metabolism of carveol and dihydrocarveol in Rhodococcus erythropolis DCL14 (Microbiology, 2000)
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Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESCC1=CCC(CC1O)C(=C)C
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InChIKeyBAVONGHXFVOKBV-UHFFFAOYSA-N
- Pubchem - CARVEOL
- Wikipedia - carveol
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.
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