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| | CARVEOL Basic information |
| Product Name: | CARVEOL | | Synonyms: | carveol,2-methyl-5-(1-methylethenyl)-2-cyclohexenol;2-Cyclohexen-1-ol, 2-methyl-5-(1-methylethenyl)-;PARA-MENTHA-6,8-DIEN-2-OL,L-;PARA-MENTHA-1,8-DIEN-6-OL;(-)-Carveol, mixture of isomers, p-Mentha-6,8-dien-2-ol;L-Carveol, mixture of cis and trans;(-)-Carveol, 95%, mixture of isomers;2-Methyl-5-isopropenyl-1-cyclohexene-3-ol | | CAS: | 99-48-9 | | MF: | C10H16O | | MW: | 152.23 | | EINECS: | 202-757-4 | | Product Categories: | | | Mol File: | 99-48-9.mol |  |
| | CARVEOL Chemical Properties |
| 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) | | pka | 14.60±0.60(Predicted) | | form | neat | | color | Clear Colourless to Light Yellow | | Specific Gravity | 0.96 | | Odor | at 100.00 %. minty spearmint cooling green herbal caraway spicy | | Odor Type | minty | | optical activity | [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 | | LogP | 3.120 | | EPA Substance Registry System | Carveol (99-48-9) |
| Hazard Codes | Xi | | Risk Statements | 36/37/38 | | Safety Statements | 26-37/39 | | WGK Germany | 2 | | RTECS | OS8400000 | | TSCA | Yes | | HS Code | 29061900 |
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ACROS
| English |
| | CARVEOL Usage And Synthesis |
| Chemical Properties | Clear colorless to slightly yellow liquid | | Chemical Properties | Carveol has spearmint-like odor. | | 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. | | 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. | | Aroma threshold values | Detection: 4 ppm | | 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. | | 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. |
| | CARVEOL Preparation Products And Raw materials |
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