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amyrin palmitate
olean-12-en-3-ol, hexadecanoate, (3b)-

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Name:[(3S,6aR,6bS,8aR,12aS,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-yl] hexadecanoate
CAS Number: 5973-06-8Picture of molecule3D/inchi
FDA UNII: Search
XlogP3-AA:17.10 (est)
Molecular Weight:665.14200000
Formula:C46 H80 O2
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
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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
Boiling Point: 661.44 °C. @ 760.00 mm Hg (est)
Flash Point: 669.00 °F. TCC ( 354.10 °C. ) (est)
logP (o/w): 18.579 (est)
Soluble in:
 water, 1.574e-013 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
BOC Sciences
For experimental / research use only.
b-Amyrin palmitate > 95%
Odor: characteristic
Use: ?-Amyrin palmitate isolated from the root of Periploca sepium Bung. It may release norepinephrine from newly synthesized pools to activate noradrenergic activity. And It has similar properties with mianserin in some respects, possessing a sedative action
Coompo
For experimental / research use only.
beta-Amyrin Palmitate from Plants ≥96%
Odor: characteristic
Use: beta-Amyrin palmitate, like mianserin and imipramine, reduced the duration of immobility of mice significantly in a dose-dependent manner (5, 10 and 20 mg kg-1). beta-Amyrin palmitate (5, 10 and 20 mg kg-1) or mianserin (5, 10 and 20 mg kg-1) elicited a dose-related reduction in locomotor activity of mice and antagonized locomotor stimulation induced by methamphetamine. In contrast, imipramine (5, 10 and 20 mg kg-1) increased locomotor activity and potentiated methamphetamine-induced hyperactivity. beta-Amyrin palmitate showed no effect on reserpine-induced hypothermia, whilst mianserin (10 mg kg-1) and imipramine (10 and 20 mg kg-1) antagonized the reserpine-induced effect. beta-amyrin palmitate has similar properties in some respects to mianserin and might possess a sedative action. beta-Amyrin palmitate might release norepinephrine from newly synthesized pools, and thus, it might activate noradrenergic activity.
 
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 amyrin palmitate usage levels up to:
 not for fragrance use.
 
Recommendation for amyrin palmitate 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 :165382
National Institute of Allergy and Infectious Diseases:Data
[(3S,6aR,6bS,8aR,12aS,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-yl] hexadecanoate
Chemidplus:0005973068
 
References:
 [(3S,6aR,6bS,8aR,12aS,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-yl] hexadecanoate
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):165382
Pubchem (sid):135121754
 
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
HMDB (The Human Metabolome Database):HMDB36660
FooDB:FDB015587
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
 elder black elder leaf
Search Trop Picture
 periploca sepium root
Search Trop Picture
 sandalwood
Search Trop Picture
 
Synonyms:
alpha-amyrin palmitate
[(3S,6aR,6bS,8aR,12aS,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-yl] hexadecanoate
 olean-12-en-3-ol, hexadecanoate, (3b)-
 

Articles:

PubMed:Promising anti-diabetes mellitus activity in rats of β-amyrin palmitate isolated from Hemidesmus indicus roots.
PubMed:β-Amyrin acetate and β-amyrin palmitate as antidyslipidemic agents from Wrightia tomentosa leaves.
PubMed:Pharmacological properties of beta-amyrin palmitate, a novel centrally acting compound, isolated from Lobelia inflata leaves.
PubMed:A possible mechanism of antidepressant activity of beta-amyrin palmitate isolated from Lobelia inflata leaves in the forced swimming test.
PubMed:An alpha-adrenoceptor-mediated mechanism of hypoactivity induced by beta-amyrin palmitate.
PubMed:Effect of alpha-amyrin palmitate on adjuvant arthritis.
PubMed:Chemical constituents of flowers and fruits of Rabdosia excisa.
PubMed:Bioactive triterpenes from Diospyros blancoi.
PubMed:Two new triterpene esters from the twigs of Brachylaena ramiflora from the Madagascar rainforest.
PubMed:Antiinflammatory activity of a Ghanaian antiarthritic herbal preparation: III.
PubMed:Oleanane-type triterpenes from Ludwigia octovalvis.
PubMed:Inhibition of serine proteases by anti-inflammatory triterpenoids.
PubMed:An antidepressant principle of Lobelia inflata L. (Campanulaceae).
PubMed:A new fatty acid ester of triterpenoid from Celastrus rosthornianus with anti-tumor activitives.
PubMed:[Studies on the chemical constituents of Carduus crispus L].
 
Notes:
Isol. from Santalum album (sandalwood). Flavouring ingredient
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