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

(S)-oleuropeic acid

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CAS Number: 5027-76-9Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J14.268I
XlogP3-AA:1.20 (est)
Molecular Weight:184.23512000
Formula:C10 H16 O3
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
Soluble in:
 water, 6855 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.
Oleuropeic acid
 
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 (S)-oleuropeic acid usage levels up to:
 not for fragrance use.
 
Recommendation for (S)-oleuropeic 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 :188320
National Institute of Allergy and Infectious Diseases:Data
(4S)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylic acid
Chemidplus:0005027769
 
References:
 (4S)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):188320
Pubchem (cas):5027-76-9
 
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):HMDB36998
FooDB:FDB015973
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
 olea europaea
Search Trop Picture
 
Synonyms:
1-cyclohexene-1-carboxylicacid, 4-(1-hydroxy-1-methylethyl)-, (4S)-
(4S)-4-(2-hydroxypropan-2-yl)cyclohexene-1-carboxylic acid
 

Articles:

PubMed:Radical-scavenging compounds from olive tree (Olea europaea L.) wood.
PubMed:Localization of oleuropeyl glucose esters and a flavanone to secretory cavities of Myrtaceae.
PubMed:Multiphoton fluorescence lifetime imaging shows spatial segregation of secondary metabolites in Eucalyptus secretory cavities.
PubMed:Phenolic compounds from the branches of Eucalyptus maideni.
PubMed:Identification of hypoglycaemic compounds from berries of Juniperus oxycedrus subsp. oxycedrus through bioactivity guided isolation technique.
PubMed:α,β-Unsaturated monoterpene acid glucose esters: structural diversity, bioactivities and functional roles.
PubMed:Synthesis of the monoterpenoid esters cypellocarpin C and cuniloside B and evidence for their widespread occurrence in Eucalyptus.
PubMed:Phloroglucinol glycosides from the fresh fruits of Eucalyptus maideni.
PubMed:Eucalmaidins A-E, (+)-oleuropeic acid derivatives from the fresh leaves of Eucalyptus maideni.
PubMed:Non-volatile components of the essential oil secretory cavities of Eucalyptus leaves: discovery of two glucose monoterpene esters, cuniloside B and froggattiside A.
PubMed:Biotransformation of alpha-terpineol by the larvae of common cutworm (Spodoptera litura).
PubMed:Cypellocarpins A-C, phenol glycosides esterified with oleuropeic acid, from Eucalyptus cypellocarpa.
PubMed:Metabolism of alpha-terpineol by Pseudomonas incognita.
 
Notes:
None found
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