- DIHYDROACTINIDIOLIDE
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- $0.00 / 1kg
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2024-07-18
- CAS:15356-74-8
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 10ton
- Dihydroactinidiolide
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- $180.00 / 1kg
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2024-05-31
- CAS:15356-74-8
- Min. Order: 1kg
- Purity: 99%
- Supply Ability: 20ton
- DIHYDROACTINIDIOLIDE
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- $10.00 / 1KG
-
2019-07-06
- CAS:15356-74-8
- Min. Order: 25KG
- Purity: 99%
- Supply Ability: 1000KGS
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| | DIHYDROACTINIDIOLIDE Basic information |
| Product Name: | DIHYDROACTINIDIOLIDE | | Synonyms: | (2,6,6-trimethy1-2-hydroxycyclohexylidene)-acetic acid lactone;4,4,7a-Trimethyl-5,6,7,7a-tetrahydro-1-benzofuran-2(4H)-one;4,5,7,7a-Tetrahydro-4,4,7a-trimethyl-2(6H)benzofuranone;4,4,7a-Trimethyl-2,4,5,6,7,7a-hexahydrobenzofuran-2-one;4,4,7a-Trimethyl-5,6,7,7a-tetrahydrobenzofuran-2(4H)-one;Dihydroactinolide;2,4,5,6,7,7a-Hexahydro-4,4,7a-trimethylbenzofuran-2-one;2-Hydroxy-2,6,6-trimethylcyclohexylidene-1-acetic acid lactone | | CAS: | 15356-74-8 | | MF: | C11H16O2 | | MW: | 180.24 | | EINECS: | 239-390-4 | | Product Categories: | | | Mol File: | 15356-74-8.mol |  |
| | DIHYDROACTINIDIOLIDE Chemical Properties |
| Melting point | 42-43° | | Boiling point | 296℃ | | density | 1.05 | | FEMA | 4020 | (+/-)-(2,6,6-TRIMETHYL-2-HYDROXYCYCLOHEXYLIDENE)ACETIC ACID GAMMA-LACTONE | | Fp | 120℃ | | storage temp. | 2-8°C | | solubility | Chloroform (Slightly), DMSO (Slightly), Methanol (Slightly) | | form | Solid | | color | Off-White | | Odor | at 100.00 %. ripe apricot fruity plum berry grape tropical fruit woody | | Odor Type | fruity | | JECFA Number | 1164 | | LogP | 2.26 | | EPA Substance Registry System | 2(4H)-Benzofuranone, 5,6,7,7a-tetrahydro-4,4,7a-trimethyl- (15356-74-8) |
| | DIHYDROACTINIDIOLIDE Usage And Synthesis |
| Chemical Properties | (+/–)-(2,6,6-Trimethyl-2-hydroxycyclohexylidene) acetic acid gamma-lactone has a powerful musky or coumarin like
odor. As this compound is formed from photooxidation of carotene-like structures, its taste is related to certain fruit types at their
peak of ripeness. | | Occurrence | Reportedly present in lemongrass and sweet grass oil. | | Preparation | Prepared in a patented process by degradation of beta-carotene in the presence of nitrogen and air. | | Definition | ChEBI: Dihydroactinidiolide is a member of benzofurans. |
| | DIHYDROACTINIDIOLIDE Preparation Products And Raw materials |
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