(-)-Carveol
(-)-Carveol structure
|
Common Name | (-)-Carveol | ||
|---|---|---|---|---|
| CAS Number | 99-48-9 | Molecular Weight | 152.233 | |
| Density | 0.9±0.1 g/cm3 | Boiling Point | 231.5±40.0 °C at 760 mmHg | |
| Molecular Formula | C10H16O | Melting Point | N/A | |
| MSDS | Chinese USA | Flash Point | 98.3±0.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
|
Inhibition by menthol and its related chemicals of compound action potentials in frog sciatic nerves.
Life Sci. 92(6-7) , 359-67, (2013) Transient receptor potential (TRP) vanilloid-1 (TRPV1) and melastatin-8 (TRPM8) channels play a role in transmitting sensory information in primary-afferent neurons. TRPV1 agonists at high concentrations inhibit action potential conduction in the neurons and ... |
|
|
Chemical composition and larvicidal activity of essential oil from Mentha spicata (Linn.) against three mosquito species.
Parasitol. Res. 110(5) , 2023-32, (2012) Mosquitoes are blood-feeding insects and serve as the most important vectors for spreading human diseases such as malaria, yellow fever, dengue fever, and filariasis. The continued use of synthetic insecticides has resulted in resistance in mosquitoes. Synthe... |
|
|
A glandular trichome-specific monoterpene alcohol dehydrogenase from Artemisia annua.
Phytochemistry 71(11-12) , 1264-9, (2010) The major components of the isoprenoid-rich essential oil of Artemisia annua L. accumulate in the subcuticular sac of glandular secretory trichomes. As part of an effort to understand isoprenoid biosynthesis in A. annua, an expressed sequence tag (EST) collec... |
|
|
Hydroxylation of limonene enantiomers and analogs by recombinant (-)-limonene 3- and 6-hydroxylases from mint (Mentha) species: evidence for catalysis within sterically constrained active sites.
Arch. Biochem. Biophys. 387(1) , 125-36, (2001) Limonene enantiomers and substrate analogs, including specifically fluorinated derivatives, were utilized to probe active site interactions with recombinant (-)-(4S)-limonene-3-hydroxylase (CYP71D13) and (-)-(4S)-limonene-6-hydroxylase (CYP71D18) from mint (M... |
|
|
Distinct effects of carvone analogues on the isolated nerve of rats.
Eur. J. Pharmacol. 645(1-3) , 108-12, (2010) Carvone (p-mentha-6,8-dien-2-one) is a monoterpene ketone found as the main active component of various essential oils. It is obtained by distillation and occurs naturally as the enantiomers (+)- and (-)-carvone. Our group have shown that the in vivo antinoci... |
|
|
Fragrance material review on carveol.
Food Chem. Toxicol. 46 Suppl 11 , S85-7, (2008) A toxicologic and dermatologic review of carveol when used as a fragrance ingredient is presented. |
|
|
Preventing biofilm formation: promoting cell separation with terpenes.
FEMS Microbiol. Ecol. 61(3) , 406-13, (2007) Both carveol and carvone were effective in dispersing Rhodococcus erythropolis cells that were being stimulated to aggregate by the presence of organic solvents. The two terpenes influenced the fatty acid composition of the cell membrane, decreasing the perce... |
|
|
Fragrance material review on laevo-carveol.
Food Chem. Toxicol. 46 Suppl 11 , S88-90, (2008) A toxicologic and dermatologic review of laevo-carveol when used as a fragrance ingredient is presented. |
|
|
Inhibitory effects of substrate and product on the carvone biotransformation activity of Rhodococcus erythropolis.
Biotechnol. Lett. 30(7) , 1245-50, (2008) The aqueous substrate and product toxicity thresholds in the microbial biotransformation of (-)-trans-carveol to the fragrance/flavor compound (R)-(-)-carvone by Rhodococcus erythropolis were determined. Above aqueous phase concentrations of approx. 500 mg ca... |
|
|
Influence of different extraction parameters on a solid-phase dynamic extraction for the gas chromatographic determination of d-limonene degradation products by using a fractional factorial design.
J. AOAC Int. 90(6) , 1623-7, (2007) Through the application of a solid-phase dynamic extraction (SPDE) method for the determination of volatile substances, different parameters may influence the extraction and desorption process and are, therefore, vital for the determination of the extracted s... |