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

myrianthic acid

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CAS Number: 89786-84-5Picture of molecule3D/inchi
Other(deleted CASRN):65669-84-3
FDA UNII: Search
Nikkaji Web:J1.358.980A
XlogP3-AA:4.30 (est)
Molecular Weight:504.70776000
Formula:C30 H48 O6
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
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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
Soluble in:
 water, 0.9074 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.
Myrianthic acid >95%
Odor: characteristic
Use: Myrianthic acid is a natural triterpenoid compound found in several plants.
 
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 myrianthic acid usage levels up to:
 not for fragrance use.
 
Recommendation for myrianthic acid 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 :182497
National Institute of Allergy and Infectious Diseases:Data
(1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
Chemidplus:0089786845
 
References:
 (1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):182497
Pubchem (cas):89786-84-5
 
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
CHEMBL:View
HMDB (The Human Metabolome Database):Search
FooDB:FDB014656
VCF-Online:VCF Volatile Compounds in Food
ChemSpider:View
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 coleus amboinicus
Search Trop Picture
 
Synonyms:
(1R,2R,4aS,6aR,6aS,6bR,8aR,9R,10S,11R,12aR,14bS)-1,10,11-trihydroxy-9-(hydroxymethyl)-1,2,6a,6b,9,12a-hexamethyl-2,3,4,5,6,6a,7,8,8a,10,11,12,13,14b-tetradecahydropicene-4a-carboxylic acid
 urs-12-en-28-oic acid, 2,3,19,23-tetrahydroxy-, (2alpha,3alpha,4alpha)-
 

Articles:

PubMed:Biological activities of triterpenoids from Poraqueiba sericea stems.
PubMed:[Triterpenoids from roots of Rosa laevigata].
PubMed:[Triterpene constituents from Rosa cymosa Tratt].
PubMed:Triterpenoids from the fruits and leaves of the blackberry (Rubus allegheniensis) and their inhibitory activities on foam cell formation in human monocyte-derived macrophage.
PubMed:[Studies on the chemical constituents of Callicarpa kochiana].
PubMed:Delavayol, a novel sesquiterpene from Incarvillea delavayi Bureau et Franchet.
PubMed:Hepatoprotective effects of Rubus aleaefolius Poir. and identification of its active constituents.
PubMed:[Triterpenes from herb of Potentilla chinesis].
PubMed:Insulin-mimetic and insulin-sensitizing activities of a pentacyclic triterpenoid insulin receptor activator.
PubMed:24-nor-Ursane type triterpenoids from the stems of Rumex japonicus.
PubMed:Anti-platelet pentacyclic triterpenoids from leaves of Campsis grandiflora.
PubMed:Pentacyclic triterpenoid and saponins from Gambeya boukokoensis.
PubMed:Flavanone glycosides from Miconia trailii.
PubMed:Triterpene phytoalexins from strawberry fruit.
 
Notes:
None found
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