beta-amyrin

olean-12-en-3beta-ol

CAS: 559-70-6 C30 H50 O MW: 426.72770000

Identification

Namebeta-amyrin
IUPAC(3S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b-octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol
CAS Number559-70-6
EINECS209-204-6
FDA UNIIKM8353IPSO
Molecular FormulaC30 H50 O
Molecular Weight426.72770000
MDL NumberMFCD00017381
Nikkaji NumberJ6.490D
Beilstein2063468

Regulatory

Physical Properties

Assay 95.00 to 100.00
Food Chemicals Codex Listed No
Melting Point 197.00 °C. @ 760.00 mm Hg
Boiling Point 490.67 °C. @ 760.00 mm Hg (est)
Flash Point 424.00 °F. TCC ( 217.70 °C. ) (est)
logP (o/w) 10.481 (est)
Soluble in water, 9.552e-005 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 beta-amyrin usage levels up tonot for fragrance use.
Recommendation for beta-amyrin flavor usage levels up tonot for flavor use.

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Potential Uses

None Found

Natural Occurrence

anise seed basswood leaf bilberry leaf broccoli asparagus broccoli bud buckwheat seed burdock leaf burdock plant cantaloupe seed carrot root chicory seed coconut seed oil corn shoot cotton plant cucumber fruit dandelion dandelion flower dandelion root date palm pollen elder black elder flower evening-primrose fruit evening-primrose inflorescence evening-primrose seed fig leaf grape leaf grape stem guava fruit melon bitter melon seed oil nance olive leaf pea seed pepper bell pepper seed rosemary rosemary plant rosemary shoot sage leaf salvia lavandulifolia vahl. leaf oil @ 0.80% Data sesame seed oil shea tree plant shea tree seed oil soybean seed soybean sprout sunflower seed tea leaf oil tea seed oil tomato fruit wheat seed

Synonyms

b- amyrenol beta- amyrenol amyrin b- amyrin (3S,4aR,5R,6aR,6bR,8S,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b- octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-eicosahydro-picen-3-ol (3S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b- octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydro-3-picenol (3S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b- octamethyl-1,2,3,4,4a,5,6,6a,6b,7,8,8a,9,10,11,12,12a,14,14a,14b-icosahydropicen-3-ol (3S,4aR,6aR,6bS,8aR,12aR,14aR,14bR)-4,4,6a,6b,8a,11,11,14b- octamethyl-1,2,3,4a,5,6,7,8,9,10,12,12a,14,14a-tetradecahydropicen-3-ol (3beta)- olean-12-en-3-ol olean-12-en-3b-ol olean-12-en-3beta-ol PubMed: Changes in the triterpenoid content of cuticular waxes during fruit ripening of eight grape (Vitis vinifera) cultivars grown in the Upper Rhine Valley. PubMed: [Triterpene compounds of Ainsliaea yunnanensis]. PubMed: Discovery of soluble epoxide hydrolase inhibitors from natural products. PubMed: Vitiquinolone--a quinolone alkaloid from Hibiscus vitifolius Linn. PubMed: Triterpenoid content of berries and leaves of bilberry Vaccinium myrtillus from Finland and Poland. PubMed: Comparison of the triterpenoid content of berries and leaves of lingonberry Vaccinium vitis-idaea from Finland and Poland. PubMed: An unusual plant triterpene synthase with predominant α-amyrin-producing activity identified by characterizing oxidosqualene cyclases from Malus × domestica. PubMed: Xanthine oxidase inhibitory triterpenoid and phloroglucinol from guttiferaceous plants inhibit growth and induced apoptosis in human NTUB1 cells through a ROS-dependent mechanism. PubMed: High throughput screening of mutants of oat that are defective in triterpene synthesis. PubMed: New triterpenoids and other constituents from a special microbial-fermented tea-Fuzhuan brick tea. PubMed: Separation and identification of some common isomeric plant triterpenoids by thin-layer chromatography and high-performance liquid chromatography. PubMed: A new fatty acid ester of triterpenoid from Celastrus rosthornianus with anti-tumor activitives. PubMed: Triterpenoids from swallow roots--a convenient HPLC method for separation. PubMed: Variation of chemical composition of the lipophilic extracts from yellow birch (Betula alleghaniensis) foliage. PubMed: Recycling plant wax constituents for chemical defense: hemi-biosynthesis of triterpene saponins from beta-amyrin in a leaf beetle. PubMed: Phytosterol content in American ginseng seed oil.