3-acetyl lupeol
lupeyl acetate
Identification
| Name | 3-acetyl lupeol |
| IUPAC | [(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate |
| CAS Number | 1617-68-1 |
| EINECS | 216-575-8 |
| FDA UNII | WJ3A89G0H6 |
| Molecular Formula | C32 H52 O2 |
| Molecular Weight | 468.76484000 |
| MDL Number | MFCD00017362 |
| Nikkaji Number | J145.292D |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Boiling Point | 502.70 °C. @ 760.00 mm Hg (est) |
| Flash Point | 490.00 °F. TCC ( 254.70 °C. ) (est) |
| logP (o/w) | 11.870 (est) |
| Soluble in | water, 2.041e-006 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| Category | natural substances and extractives |
| Recommendation for 3-acetyl lupeol usage levels up to | not for fragrance use. |
| Recommendation for 3-acetyl lupeol flavor usage levels up to | not for flavor use. |
BOC Sciences
Best of Chemicals Supplier
Quality supplier of research chemicals and biochemicals including inhibitors, building blocks, GMP Products, impurities and metabolites, APIs for Veterinary, Natural Compounds, ADCs, Stem Cell Molecul...
Potential Uses
Natural Occurrence
Synonyms
3-
acetyllupeol
[(1R,3aR,5aR,5bR,7aR,9S,11aR,11bR,13aR,13bR)-3a,5a,5b,8,8,11a-
hexamethyl-1-prop-1-en-2-yl-1,2,3,4,5,6,7,7a,9,10,11,11b,12,13,13a,13b-hexadecahydrocyclopenta[a]chrysen-9-yl] acetate
lup-20(29)-en-3-ol, acetate, (3beta)-
lup-20(29)-en-3beta-ol, acetate (8CI)
lupeol acetate
lupeyl acetate
PubMed:
Occurrence and sources of triterpenoid methyl ethers and acetates in sediments of the cross-river system, southeast Nigeria.
PubMed:
[Isolation and identification of the lipophilic constituents from the root of Euphorbia fischeriana Steud].
PubMed:
New lupane triterpenoids from Solidago canadensis that inhibit the lyase activity of DNA polymerase beta.
PubMed:
Two new triterpene esters from the twigs of Brachylaena ramiflora from the Madagascar rainforest.
PubMed:
New cytotoxic terpenoids from the wood of Vepris punctata from the Madagascar Rainforest.
PubMed:
New cytotoxic lupane triterpenoids from the twigs of Coussarea paniculata.