- (+)-Dihydrocarvone
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- $15.00 / 1KG
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2021-07-02
- CAS:5524-05-0
- Min. Order: 1KG
- Purity: 99%+ HPLC
- Supply Ability: Monthly supply of 1 ton
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| | (+)-DIHYDROCARVONE MIXTURE OF ISOMERS Basic information |
| Product Name: | (+)-DIHYDROCARVONE MIXTURE OF ISOMERS | | Synonyms: | (2S,5R)-2-methyl-5-(1-methylethenyl)-1-cyclohexanone;(+)-dihydrocarvone,mixtureofisomers;(2theta-trans)-cyclohexanon;2-methyl-5-(1-methylethenyl)-,(2R-trans)-Cyclohexanone;Carvone,dihydro-;Cyclohexanone,2-methyl-5-(1-methylethenyl)-,(2R,5R)-rel-;Cyclohexanone,2-methyl-5-(1-methylethenyl)-,trans-;p-Menth-8-en-2-one,trans- | | CAS: | 5524-05-0 | | MF: | C10H16O | | MW: | 152.23 | | EINECS: | 226-872-4 | | Product Categories: | | | Mol File: | 5524-05-0.mol |  |
| | (+)-DIHYDROCARVONE MIXTURE OF ISOMERS Chemical Properties |
| alpha | +17°(22℃,neat) | | Boiling point | 87-88°C/6mmHg | | density | 0.928 g/mL at 20 °C(lit.) | | FEMA | 3565 | P-MENTH-8-EN-2-ONE | | refractive index | n20/D 1.471 | | Fp | 102 °C | | storage temp. | Sealed in dry,Room Temperature | | solubility | Chloroform (Sparingly), Ethyl Acetate (Slightly), Methanol (Slightly) | | form | Liquid | | Specific Gravity | 0.929 | | color | Clear | | Odor | at 100.00 %. herbal minty mentholic | | Odor Type | minty | | Optical Rotation | [α]20/D +20±2°, neat | | JECFA Number | 377 | | BRN | 2044615 | | InChI | 1S/C10H16O/c1-7(2)9-5-4-8(3)10(11)6-9/h8-9H,1,4-6H2,2-3H3 | | InChIKey | AZOCECCLWFDTAP-UHFFFAOYSA-N | | SMILES | CC1CCC(CC1=O)C(C)=C | | LogP | 3.225 (est) | | EPA Substance Registry System | Cyclohexanone, 2-methyl-5-(1-methylethenyl)-, (2R,5R)- (5524-05-0) |
| Safety Statements | 23-24/25 | | WGK Germany | 3 | | TSCA | TSCA listed | | HS Code | 29142900 | | Storage Class | 10 - Combustible liquids |
| | (+)-DIHYDROCARVONE MIXTURE OF ISOMERS Usage And Synthesis |
| Chemical Properties | clear liquid | | Uses | (+)-Dihydrocarvone may be used in the following processes:
- Synthesis of dispiro 1,2,4,5-tetraoxanes, which show potent anti-malarial activity.
- Synthesis of an epoxylactone by oxidation, which can undergo copolymerization with ε-caprolactone to form cross-linked copolymers with shape memory properties.
- Synthesis of α-Cyperone, a eudesmane type sesquiterpenoid compound with potent insecticidal activity.
| | Definition | ChEBI: A dihydrocarvone in (R,R) configuration. | | General Description | (+)-Dihydrocarvone, a monoterpenoid compound found in caraway oil, is a key building block to synthesize sesquiterpenes. It is generally produced either by the hydrogenation of carvone or oxidation of limonene. |
| | (+)-DIHYDROCARVONE MIXTURE OF ISOMERS Preparation Products And Raw materials |
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