methyl oleanolate

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olean-12-en-28-oic acid, 3-hydroxy-, methyl ester, (3beta)-

CAS: 1724-17-0 C31 H50 O3 MW: 470.73710000
All Ingredients Aromatic Ingredients CAS Numbers EINECS Numbers Found in Nature

Identification

Namemethyl oleanolate
IUPACmethyl (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate
CAS Number1724-17-0
EINECS217-029-1
FDA UNIISearch
Molecular FormulaC31 H50 O3
Molecular Weight470.73710000
Nikkaji NumberJ203.120E

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Boiling Point 526.10 °C. @ 760.00 mm Hg (est)
Flash Point 375.00 °F. TCC ( 190.70 °C. ) (est)
logP (o/w) 9.520 (est)
Soluble in water, 0.0003266 mg/L @ 25 °C (est)

No sensory data available

Safety Information

Oral/Parenteral ToxicityNot determined
Dermal ToxicityNot determined
Inhalation ToxicityNot determined

GHS Classification

['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']

Safety in Use

Categorynatural substances and extractives
Recommendation for methyl oleanolate usage levels up tonot for fragrance use.
Recommendation for methyl oleanolate flavor usage levels up tonot for flavor use.

No supplier data available

Potential Uses

None Found

Natural Occurrence

grape leaf

Synonyms

methyl (3beta)-3-hydroxyolean-12-en-28-oate methyl (4aS,6aR,6aS,6bR,8aR,10S,12aR,14bS)-10-hydroxy-2,2,6a,6b,9,9,12a-heptamethyl-1,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylate methyloleanolate olean-12-en-28-oic acid, 3-hydroxy-, methyl ester, (3beta)- oleanolic acid methyl ester oleanolic acid methylester PubMed: C-lactam derivatives of oleanolic acid. hydrolysis and further acylation of methyl acetyloleanolate C-lactam and C-thiolactam. PubMed: [Study on constituents of the aerial parts of Pogostemon cablin]. PubMed: The analgesic and anti-inflammatory effect of new oleanolic acid acyloxyimino derivative. PubMed: [Study on the triterpenoids from the fruits of Ligustrum lucidum]. PubMed: Anticancer effect of A-ring or/and C-ring modified oleanolic acid derivatives on KB, MCF-7 and HeLa cell lines. PubMed: [Chemical constituents of Incarvillea younghusbandii]. PubMed: Kalaic acid, a new ursane-type saponin from Musanga cecropioides. PubMed: Triterpenoids. Part 21: Oleanolic acid azaderivatives as percutaneous transport promoters. PubMed: Structure-activity relationships of synthetic saponins.