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oleoside 11-methyl ester

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CAS Number: 60539-23-3Picture of molecule3D/inchi
FDA UNII: Search
Nikkaji Web:J510.902G
XlogP3-AA:-2.00 (est)
Molecular Weight:404.36948000
Formula:C17 H24 O11
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
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Google Patents:Search
US Patents:Search
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Pubchem Patents:Search
PubMed:Search
NCBI:Search
 
Physical Properties:
Assay: 95.00 to 100.00
Food Chemicals Codex Listed: No
Soluble in:
 water, 1.665e+005 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.
Oleoside 11-methyl ester 98%
Odor: characteristic
Use: Oleoside 11-methyl ester is an iridoid isolated from Ligustrum lucidum.
 
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 oleoside 11-methyl ester usage levels up to:
 not for fragrance use.
 
Recommendation for oleoside 11-methyl ester 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 :10692563
National Institute of Allergy and Infectious Diseases:Data
2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetic acid
 
References:
 2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):10692563
Pubchem (cas):60539-23-3
 
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):HMDB41550
FooDB:FDB021533
VCF-Online:VCF Volatile Compounds in Food
 
Potential Blenders and core components note
None Found
 
Potential Uses:
None Found
 
Occurrence (nature, food, other):note
 jasminum sambac
Search Trop Picture
 
Synonyms:
2-[(2S,3E,4S)-3-ethylidene-5-methoxycarbonyl-2-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy-4H-pyran-4-yl]acetic acid
 oleoside methyl ester
 

Articles:

PubMed:Lignans and secoiridoid glycosides from the stem barks of Jasminum tortuosum.
PubMed:Hydroxycinnamoyl derivatives and secoiridoid glycoside derivatives from Syringa vulgaris flowers and their effects on the pro-inflammatory responses of human neutrophils.
PubMed:Structure-activity relationships of fraxamoside as an unusual xanthine oxidase inhibitor.
PubMed:Survival of foodborne pathogens in natural cracked olive brines.
PubMed:Ultrahigh-pressure liquid chromatography triple-quadrupole tandem mass spectrometry quantitation of polyphenols and secoiridoids in california-style black ripe olives and dry salt-cured olives.
PubMed:Phenolic profile characterization of Chemlali olive stones by liquid chromatography-ion trap mass spectrometry.
PubMed:Metabolites involved in oleuropein accumulation and degradation in fruits of Olea europaea L.: Hojiblanca and Arbequina varieties.
PubMed:Structural revision of oleoacteoside and oleoechinacoside.
PubMed:Iridoids from Fraxinus excelsior with adipocyte differentiation-inhibitory and PPARalpha activation activity.
PubMed:Inhibitors of lactic acid fermentation in Spanish-style green olive brines of the Manzanilla variety.
PubMed:[Glycosides from flowers of Jasminum officinale L. var. grandiflorum].
PubMed:Main antimicrobial compounds in table olives.
PubMed:Oligomeric secoiridoid glucosides from Jasminum abyssinicum.
PubMed:Isolation of an angiotensin converting enzyme (ACE) inhibitor from Olea europaea and Olea lancea.
 
Notes:
None found
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