| Identification | Back Directory | [Name]
CARVEOL | [CAS]
99-48-9 | [Synonyms]
CARVEOL
NSC 68313
L-Carveol,97%
L-CARVEOL 95+%
P-MENTHA-6,8-DIEN-2-OL
p-Mentha-1,8-dien-6-ol
p-mentha-1(6),8-dien-2-ol
PARA-MENTHA-1,8-DIEN-6-OL
p-Mentha-6,8-dien-2-ol, l-
p-Mentha-1(6),8-diene-2-ol
PARA-MENTHA-6,8-DIEN-2-OL,L-
(-)-carveol,mixtureofisomers
Carveol (Mixture of cis and trans)
(-)-Carveol, mixture of isomers 97%
(-)-Carveol, 95%, mixture of isomers
(-)-CARVEOL, 97%, MIXTURE OF ISOMERS
5-Isopropenyl-2-methyl-2-cyclohexen-1-ol
1-Methyl-4-isopropenyl-6-cyclohexen-2-ol
L-Carveol, mixture of cis and trans
2-Methyl-5-isopropenyl-2-cyclohexen-1-ol
2-Methyl-5-isopropenyl-1-cyclohexene-3-ol
2-Methyl-5-isopropenyl-2-cyclohexene-1-ol
2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-enol
2-Methyl-5-(1-methylethenyl)-cyclohexen-2-ol
2-methyl-5-(1-methylethenyl)-2-cyclohexen-1-o
2-methyl-5-(1-methylethenyl)-2-Cyclohexen-1-ol
2-Methyl-5(1-methylethenyl)cyclohex-2-ene-1-ol
2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-
carveol,2-methyl-5-(1-methylethenyl)-2-cyclohexenol
(-)-Carveol, mixture of isomers, p-Mentha-6,8-dien-2-ol | [EINECS(EC#)]
202-757-4 | [Molecular Formula]
C10H16O | [MDL Number]
MFCD00062993 | [MOL File]
99-48-9.mol | [Molecular Weight]
152.23 |
| Chemical Properties | Back Directory | [Appearance]
Clear colorless to slightly yellow liquid | [Melting point ]
24-25 °C | [Boiling point ]
226-227 °C751 mm Hg(lit.)
| [density ]
0.958 g/mL at 25 °C(lit.)
| [FEMA ]
2247 | CARVEOL | [refractive index ]
n20/D 1.496
| [Fp ]
209 °F
| [storage temp. ]
2-8°C
| [solubility ]
Chloroform, Ethyl Acetate (Slightly) | [form ]
neat | [pka]
14.60±0.60(Predicted) | [color ]
Clear Colourless to Light Yellow | [Specific Gravity]
0.96 | [Odor]
at 100.00 %. minty spearmint cooling green herbal caraway spicy | [biological source]
synthetic | [Odor Type]
minty | [Optical Rotation]
[α]22/D 115°, c = 1 in chloroform | [Water Solubility ]
Partly soluble in water. Soluble in alcohol, ethanol and DMSO. | [JECFA Number]
381 | [BRN ]
6269416 | [Dielectric constant]
11.2（18℃） | [Cosmetics Ingredients Functions]
PERFUMING | [InChI]
1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h4,9-11H,1,5-6H2,2-3H3/t9-,10?/m1/s1 | [InChIKey]
BAVONGHXFVOKBV-YHMJZVADSA-N | [SMILES]
CC(=C)[C@@H]1CC=C(C)C(O)C1 | [LogP]
3.120 | [EPA Substance Registry System]
Carveol (99-48-9) |
| Hazard Information | Back Directory | [Chemical Properties]
Clear colorless to slightly yellow liquid | [Definition]
ChEBI: A limonene monoterpenoid that is cyclohex-2-en-1-ol substituted by a methyl group at position 2 and a prop-1-en-2-yl group at position 5. | [General Description]
Clear colorless liquid. Insoluble in water. | [Air & Water Reactions]
Insoluble in water. | [Reactivity Profile]
Flammable and/or toxic gases are generated by the combination of alcohols with alkali metals, nitrides, and strong reducing agents. They react with oxoacids and carboxylic acids to form esters plus water. Oxidizing agents convert them to aldehydes or ketones. Alcohols exhibit both weak acid and weak base behavior. They may initiate the polymerization of isocyanates and epoxides. | [Health Hazard]
ACUTE/CHRONIC HAZARDS: Toxic. | [Occurrence]
In small amounts, sometimes esterified, it has been reported present in caraway seeds, spearmint, orange juice,
mango and eucalyptus oil. | [Uses]
Carveol, is a constituent of spearmint essential oil in the form of cis-(?)-carveol. It can be used as a fragrance ingredient, and as a flavor additive in the food industry. It is also found that its alpha-trans-dihydroxy derivative, possesses potent antiparkinsonian activity in animal models. | [Aroma threshold values]
Detection: 4 ppm | [Synthesis]
The various d-, l- and dl- (cis- and trans-, respectively) forms have been prepared synthetically and isolated by means of
the dinitrobenzoates according to Amvers’ law. They are prepared by oxidation of limonene or, better, from carvone. |
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Sigma-Aldrich
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