(+)-DIHYDROCARVONE
(+)-DIHYDROCARVONE Basic information
- Product Name:
- (+)-DIHYDROCARVONE
- Synonyms:
-
- P-MENTH-8-EN-2-ONE
- (Z)-dihydrocarvone
- 2-methyl-5-(1-methylethenyl)-cyclohexanon
- 2-Methyl-5-(1-methylethenyl)cyclohexanone
- 2-methyl-5-(1-methylethenyl)-Cyclohexanone
- 5-Isopropenyl-2-methylcyclohexanone
- cis-Dihydrocarvone
- Cyclohexanone, 2-methyl-5-(1-methylethenyl)-
- CAS:
- 7764-50-3
- MF:
- C10H16O
- MW:
- 152.23
- EINECS:
- 231-857-0
- Product Categories:
-
- Chiral Building Blocks
- Ketones
- Organic Building Blocks
- Mol File:
- 7764-50-3.mol
(+)-DIHYDROCARVONE Chemical Properties
- Boiling point:
- 87-88 °C6 mm Hg(lit.)
- Density
- 0.929 g/mL at 25 °C(lit.)
- vapor density
- 5.2 (vs air)
- vapor pressure
- 0.06 mm Hg ( 20 °C)
- refractive index
- n20/D 1.472(lit.)
- FEMA
- 3565 | P-MENTH-8-EN-2-ONE
- Flash point:
- 178 °F
- storage temp.
- 2-8°C
- Odor
- at 100.00 %. warm powerful herbal spearmint
- Odor Type
- minty
- optical activity
- [α]22/D +17°, neat
- JECFA Number
- 377
- Dielectric constant
- 8.5(19℃)
- LogP
- 2.85
- CAS DataBase Reference
- 7764-50-3
- EPA Substance Registry System
- Cyclohexanone, 2-methyl-5-(1-methylethenyl)- (7764-50-3)
Safety Information
- Hazard Codes
- Xi
- Risk Statements
- 36/37/38
- Safety Statements
- 26-36/37/39
- WGK Germany
- 3
- RTECS
- OT0305000
MSDS
- Language:English Provider:ACROS
- Language:English Provider:SigmaAldrich
(+)-DIHYDROCARVONE Usage And Synthesis
Chemical Properties
p-Menth-8-en-2-one has an herbaceous, spearmint-like odor.
Occurrence
Reported present in oregano oil, celery, spearmint oil, scotch spearmint oil, thymus, dill herb and seed and caraway seed.
Uses
The dual, herbal-minty quality of this compound will add an interesting twist to mint flavors as well as to celery, caraway, dill and herbal flavors, especially intended for cough drops and oral care products. At very low levels, it will add depth to tropical flavors like lychee, guava, passion fruit and rambutan.
Uses
The N-functionalization of dihydrocarvone forms imine derivatives, which are synthons for preparing N-heterocycles.
Preparation
The production of cis-Dihydrocarvone: 1) by Isomerization of Limonene oxide. 2) from Dihydrocarveol by oxidation - or 3) from Carvone by reduction.
Definition
ChEBI: A dihydrocarvone resulting from reduction of the endocyclic cyclohexene double bond.
Aroma threshold values
Detection: 820 ppb to 1.06 ppm
Synthesis Reference(s)
Journal of the American Chemical Society, 89, p. 2794, 1967 DOI: 10.1021/ja00987a087
Tetrahedron Letters, 30, p. 6567, 1989 DOI: 10.1016/S0040-4039(01)89023-7
General Description
Natural occurence: Caraway seed, celery seed, dill, patchouli, spearmint, buchu and pepper
Biochem/physiol Actions
Taste at 2-4ppm
Safety Profile
Moderately toxic by subcutaneous route. A skin irritant. When heated to decomposition it emits acrid smoke and irritating fumes.
(+)-DIHYDROCARVONE Preparation Products And Raw materials
Raw materials
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