(S)-oleuropeic acid
Identification
| Name | (S)-oleuropeic acid |
| CAS Number | 5027-76-9 |
| FDA UNII | Search |
| Molecular Formula | C10 H16 O3 |
| Molecular Weight | 184.23512000 |
| Nikkaji Number | J14.268I |
Regulatory
Physical Properties
| Assay | 95.00 to 100.00 |
| Food Chemicals Codex Listed | No |
| Soluble in | water, 6855 mg/L @ 25 °C (est) |
No sensory data available
Safety Information
| Oral/Parenteral Toxicity | Not determined |
| Dermal Toxicity | Not determined |
| Inhalation Toxicity | Not determined |
GHS Classification
['GHS Classification in accordance with 29 CFR 1910 (OSHA HCS)', 'GHS Label elements, including precautionary statements']
Safety in Use
| 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. |
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Potential Uses
Natural Occurrence
Synonyms
1-
cyclohexene-1-carboxylicacid, 4-(1-hydroxy-1-methylethyl)-, (4S)-
(4S)-4-(2-
hydroxypropan-2-yl)cyclohexene-1-carboxylic acid
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.