TGSC Information System

EU/US Properties Organoleptics Cosmetics Suppliers Safety Safety in use Safety references References Other Blenders Uses Occurrence Synonyms Articles Notes

beta-amyrin
olean-12-en-3beta-ol

Supplier Sponsors

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 Molecule and chiral compounds.
BOC Sciences provides a wide range of services to support the pharmaceutical industry through all stages of drug discovery including Custom Synthesis of those chemicals that are not in stock, Isotope Labeling Service, Chiral Synthesis and Resolution, Bioconjugation, PEGylation services, analytical services.
BOC Sciences is a brand of BOCSCI Inc. We leverage our wide spectrum of business in the fields of development, manufacturing, marketing, and distribution to help you make best-informed decisions tailored to your evolving needs for premium chemicals. Our complete suite of CRO services spans the entire molecule development pipeline including contract research for target identification, building blocks, compound synthesis, biochemical and cellular analysis, preclinical animal tests, and clinical studies.
Email:	Marketing
US Email:	Marketing
Email:	Sales
US Email:	Sales
Voice: 1-631-485-4226
Fax: 1-631-614-7828
US Voice: 1-631-485-4226
US Fax: 1-631-614-7828
Europe	44-203-286-1088
Facebook
Twitter
Linkedin
Blog
Get the App!
CODE105768 CODE105768
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

Name:	(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 Number:	559-70-6	3D/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, Edge 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

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)

Organoleptic Properties:

Odor and/or flavor descriptions from others (if found).

Cosmetic Information:

None found

Suppliers:

Alfa Biotechnology

For experimental / research use only.

beta-amyriin 98%

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

For experimental / research use only.

For experimental / research use only.

beta-Amyrin from Plants ≥96%

For experimental / research use only.

beta-Amyrin (HPLC) ≥98.5%

Santa Cruz Biotechnology

For experimental / research use only.

For experimental / research use only.

analytical standard

Safety Information:


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

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.

Safety References:

EPI System: View

AIDS Citations:Search

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

(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

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

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

Potential Blenders and core components note

None Found

Potential Uses:

None Found

Occurrence (nature, food, other):note

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

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

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.

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.

Top of Page Home

Copyright © 1980-2021 The Good Scents Company (tgsc) ™ Disclaimer Privacy Policy