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

6"-O-malonyl genistin
genistin 6''-O-malonate

Supplier Sponsors

CAS Number: 51011-05-3Picture of molecule3D/inchi
FDA UNII: 2AUB85VT2K
Nikkaji Web:J485.134J
MDL:MFCD02684045
XlogP3-AA:0.60 (est)
Molecular Weight:518.42894000
Formula:C24 H22 O13
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
Boiling Point: 882.51 °C. @ 760.00 mm Hg (est)
Flash Point: 577.00 °F. TCC ( 302.70 °C. ) (est)
logP (o/w): 1.668 (est)
Soluble in:
 water, 912.8 mg/L @ 25 °C (est)
 
Organoleptic Properties:
Odor and/or flavor descriptions from others (if found).
 
Cosmetic Information:
None found
 
Suppliers:
Alfa Biotechnology
For experimental / research use only.
6''-O-Malonylgenistin 98%
BOC Sciences
For experimental / research use only.
6"-O-Malonylgenistin
Carbosynth
For experimental / research use only.
6"-O-Malonylgenistin
Nacalai USA
For experimental / research use only.
6"-O-Malonylgenistin
 
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 6"-O-malonyl genistin usage levels up to:
 not for fragrance use.
 
Recommendation for 6"-O-malonyl genistin 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 :15934091
National Institute of Allergy and Infectious Diseases:Data
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-3-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid
Chemidplus:0051011053
 
References:
 3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-3-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):15934091
Pubchem (sid):162263745
 
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
CHEBI:View
CHEMBL:View
KEGG (GenomeNet):C16192
HMDB (The Human Metabolome Database):HMDB29529
FooDB:FDB000670
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
 lupine white lupine
Search Trop Picture
 soybean plant
Search Trop Picture
 soybean seed
Search Trop Picture
 
Synonyms:
 genistin 6''-O-malonate
6"-O-malonylgenistin
3-oxo-3-[[(2R,3S,4S,5R,6S)-3,4,5-trihydroxy-6-[5-hydroxy-3-(4-hydroxyphenyl)-4-oxochromen-7-yl]oxyoxan-2-yl]methoxy]propanoic acid
 

Articles:

PubMed:Detection and structural characterization of thermally generated isoflavone malonylglucoside derivatives.
PubMed:Isoflavone content and its potential contribution to the antihypertensive activity in soybean Angiotensin I converting enzyme inhibitory peptides.
PubMed:Isoflavonoid composition of a callus culture of the relict tree Maackia amurensis Rupr. et Maxim.
PubMed:Correlations of oil and protein with isoflavone concentration in soybean [Glycine max (L.) Merr.].
PubMed:Variation in isoflavone of soybean cultivars with location and storage duration.
PubMed:Isoflavone aglycon and glucoconjugate content of high- and low-soy U.K. foods used in nutritional studies.
PubMed:Preparative separation of isoflavone components in soybeans using high-speed counter-current chromatography.
 
Notes:
Present in soy foods. Potential nutriceutical
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