Carvone

Base Information Edit

Chemical Name:Carvone
CAS No.:99-49-0
Deprecated CAS:22327-39-5
Molecular Formula:C₁₀H₁₄O
Molecular Weight:150.221
Hs Code.:
European Community (EC) Number:202-759-5
NSC Number:93738,6275
UNII:75GK9XIA8I
DSSTox Substance ID:DTXSID8047426
Nikkaji Number:J4.522E
Wikipedia:Carvone
Wikidata:Q416800
Metabolomics Workbench ID:123649
ChEMBL ID:CHEMBL15676
Mol file:99-49-0.mol

Synonyms:(RS)-5-isopropenyl-2-methylcyclohex-2-en-1-one;2-methyl-5-(1-methylethenyl)-2-cyclohexene-1-one;2-methyl-5-isopropenyl-2-cyclohexenone;5-isopropyl-2-methyl-2-cyclohexen-1-one;carvone;carvone, (+--)-;carvone, (R)-isomer;carvone, (S)-isomer;limonen-6-one

Suppliers and Price of Carvone

Supply Marketing:Edit

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

TRC
Carvone
5g
$ 160.00

Chemenu
2-Methyl-5-(prop-1-en-2-yl)cyclohex-2-enone 95%
100g
$ 527.00

AK Scientific
Carvone
25g
$ 100.00

AHH
Carvone 98%
2500g
$ 418.00

Total 46 raw suppliers

Chemical Property of Carvone Edit

Chemical Property:

Vapor Pressure:0.0656mmHg at 25°C
Melting Point:230℃
Refractive Index:1.710
Boiling Point:230.5 °C at 760 mmHg
Flash Point:88.9 °C
Density:0.94 g/cm³
Storage Temp.:2-8°C
Solubility.:Chloroform (Slightly), Methanol (Slightly)
XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:150.104465066
Heavy Atom Count:11
Complexity:223

Purity/Quality:

98%,99%, ^*data from raw suppliers

Carvone ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Chemical Classes:Biological Agents -> Plant Oils and Extracts
Canonical SMILES:CC1=CCC(CC1=O)C(=C)C
Physical properties The carvones are colorless to slightly yellow liquids.(+)-Carvone has a herbaceous odor reminiscent of caraway and dill seeds, whereas (?)-carvone has a herbaceous odor reminiscent of spearmint. Depending on the reaction conditions, hydrogenation of carvone yields either carveol or dihydrocarvone, which are also used as flavor compounds. When treated with strong acids, carvone isomerizes to carvacrol.
Uses Flavoring, liqueurs, perfumery, soaps. Carvone is useful for the treatment of various metabolic disorders and GI related disorders.

Technology Process of Carvone

There total 96 articles about Carvone which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 85.0%

: 99-49-0,22327-39-5
Carvone

: 499-75-2
carvacrol

Guidance literature:

Reference yield: 33.0%

: 99-48-9,22567-18-6,20307-86-2
5-Isopropenyl-2-methyl-cyclohex-2-enol

: 18383-49-8,33204-74-9,36616-60-1,39067-90-8,39903-97-4,39903-98-5,74608-55-2,117181-65-4
carvone epoxide

: 99-49-0,22327-39-5
Carvone

Guidance literature:: With cobalt; oxygen; isobutyraldehyde; In acetonitrile; for 24h; Ambient temperature;
DOI:10.1016/S0040-4020(97)00432-8

Reference yield: 9.4%

: 5989-27-5,555-08-8,8022-90-0,9003-73-0,95327-98-3
D-limonene

: 99-49-0,22327-39-5
Carvone

: 1195-32-0
1-methyl-4-isopropenylbenzene

: 1253216-40-8,188635-29-2,22567-18-6,20307-86-2
(5S)-2-methyl-5-(1-methylvinyl)-2-cyclohexen-1-ol

: 5503-12-8
L-perillaldehyde

Guidance literature:: With tert.-butylhydroperoxide; air; iron(III) chloride; In acetic acid; acetonitrile; Product distribution; picolinic acid, time, atmosphere;
DOI:10.1016/S0040-4039(00)73340-5