beta-amyrin
olean-12-en-3beta-ol
 
Notes:
alpha-amyrin is also available; a 5 ring triterpene derived from oleanane that differs from alpha-amyrin in having the 29-carbon at the 20 position.
  • BOC Sciences
    • BOC Sciences
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      Product(s):
      559-70-6 beta-Amyrin 96%
      ?-Amyrin isolated from the stem bark of Alstonia boonei. It can enhance the total sleeping behavior in pentobarbital-induced sleeping model via the activating of GABAergic neurotransmitter system GABA content in the brain. anti-inflammatory activity
       
       
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CAS Number: 559-70-6Picture of molecule3D/inchi
ECHA EINECS - REACH Pre-Reg: 209-204-6
FDA UNII: KM8353IPSO
Nikkaji Web: J6.490D
Beilstein Number: 2063468
MDL: MFCD00017381
XlogP3-AA: 9.20 (est)
Molecular Weight: 426.72770000
Formula: C30 H50 O
BioActivity Summary: listing
NMR Predictor: Predict (works with chrome or firefox)
Category: natural substances and extractives
 
US / EU / FDA / JECFA / FEMA / FLAVIS / Scholar / Patent Information:
Google Scholar: Search
Google Books: Search
Google Scholar: with word "volatile"Search
Google Scholar: with word "flavor"Search
Google Scholar: with word "odor"Search
Google Patents: Search
US Patents: Search
EU Patents: Search
Pubchem Patents: Search
PubMed: Search
NCBI: Search
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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)
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Organoleptic Properties:
 
Odor and/or flavor descriptions from others (if found).
 
 
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Cosmetic Information:
None found
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Suppliers:
Alfa Biotechnology
For experimental / research use only.
beta-amyriin 98%
BOC Sciences
For experimental / research use only.
beta-Amyrin 96%
Odor: characteristic
Use: ?-Amyrin isolated from the stem bark of Alstonia boonei. It can enhance the total sleeping behavior in pentobarbital-induced sleeping model via the activating of GABAergic neurotransmitter system GABA content in the brain. anti-inflammatory activity
Carbosynth
For experimental / research use only.
b-Amyrin
Coompo
For experimental / research use only.
beta-Amyrin from Plants ≥96%
ExtraSynthese
For experimental / research use only.
beta-Amyrin (HPLC) ≥98.5%
Santa Cruz Biotechnology
For experimental / research use only.
beta-Amyrin
Sigma-Aldrich
For experimental / research use only.
b-Amyrin
analytical standard
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Safety Information:
Preferred SDS: View
 
Hazards identification
 
Classification of the substance or mixture
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)
None found.
GHS Label elements, including precautionary statements
 
Pictogram
 
Hazard statement(s)
None found.
Precautionary statement(s)
None found.
Oral/Parenteral Toxicity:
Not determined
Dermal Toxicity:
Not determined
Inhalation Toxicity:
Not determined
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Safety in Use Information:
Category: natural substances and extractives
Recommendation for beta-amyrin usage levels up to:
 not for fragrance use.
 
Recommendation for beta-amyrin flavor usage levels up to:
 not for flavor use.
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Safety References:
EPI System: View
Cancer Citations: Search
Toxicology Citations: Search
EPA ACToR: Toxicology Data
EPA Substance Registry Services (SRS): Registry
Laboratory Chemical Safety Summary : 73145
National Institute of Allergy and Infectious Diseases: Data
WGK Germany: 3
 (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
Chemidplus: 0000559706
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References:
 (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
NIST Chemistry WebBook: Search Inchi
Pubchem (cid): 73145
Pubchem (sid): 135029592
Pherobase: View
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Other Information:
(IUPAC): Atomic Weights of the Elements 2011 (pdf)
Videos: The Periodic Table of Videos
tgsc: Atomic Weights use for this web site
(IUPAC): Periodic Table of the Elements
CHEBI: View
CHEMBL: View
KEGG (GenomeNet): C08616
HMDB (The Human Metabolome Database): Search
FooDB: FDB004092
Typical G.C.
VCF-Online: VCF Volatile Compounds in Food
ChemSpider: View
Wikipedia: View
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Potential Blenders and core components note
 
None Found
 
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Potential Uses:
None Found
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Occurrence (nature, food, other): note
 anise seed
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 basswood leaf
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 bilberry leaf
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 broccoli asparagus broccoli bud
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 buckwheat seed
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 burdock leaf
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 burdock plant
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 cantaloupe seed
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 carrot root
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 chicory seed
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 coconut seed oil
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 corn shoot
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 cotton plant
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 cucumber fruit
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 dandelion
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 dandelion flower
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 dandelion root
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 date palm pollen
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 elder black elder flower
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 evening-primrose fruit
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 evening-primrose inflorescence
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 evening-primrose seed
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 fig leaf
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 grape leaf
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 grape stem
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 guava fruit
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 melon bitter melon seed oil
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 nance
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 olive leaf
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 pea seed
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 pepper bell pepper seed
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 rosemary
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 rosemary plant
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 rosemary shoot
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 sage leaf
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 salvia lavandulifolia vahl. leaf oil @ 0.80%
Data  GC  Search Trop  Picture
 sesame seed oil
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 shea tree plant
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 shea tree seed oil
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 soybean seed
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 soybean sprout
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 sunflower seed
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 tea leaf oil
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 tea seed oil
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 tomato fruit
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 wheat seed
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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
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Articles:
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.
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