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kaempferol 7-O-glucoside
kaempferol-7-O-beta-D-glucopyranoside

Supplier Sponsors

Name:3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
CAS Number: 16290-07-6Picture of molecule3D/inchi
FDA UNII: RZF1QN1Z8R
Nikkaji Web:J94.495E
MDL:MFCD08459623
XlogP3-AA:0.70 (est)
Molecular Weight:448.38160000
Formula:C21 H20 O11
BioActivity Summary:listing
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: 810.20 °C. @ 760.00 mm Hg (est)
Flash Point: 549.00 °F. TCC ( 287.00 °C. ) (est)
logP (o/w): -0.190 (est)
Soluble in:
 water, 6409 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.
Kaempferol-7-O-β-D-glucoside 98%
BOC Sciences
For experimental / research use only.
Kaempferol-7-O-glucoside >98%
Odor: characteristic
Use: Kaempferol-7-O-?-D-glucopyranoside is extracted from the herbs of Hosta plantaginea.
ExtraSynthese
For experimental / research use only.
Kaempferol-7-O-glucoside (HPLC) ≥90%
Sigma-Aldrich: Sigma
For experimental / research use only.
Kaempferol 7-O-β -D-glucopyranoside ≥90.0% (HPLC)
 
Safety Information:
Preferred SDS: View
 
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 kaempferol 7-O-glucoside usage levels up to:
 not for fragrance use.
 
Recommendation for kaempferol 7-O-glucoside 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 :10095180
National Institute of Allergy and Infectious Diseases:Data
WGK Germany:3
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
Chemidplus:0016290076
 
References:
 3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):10095180
Pubchem (sid):172648475
 
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
HMDB (The Human Metabolome Database):Search
FooDB:FDB016495
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
 bean fava bean fruit
Search Trop Picture
 bean mat bean
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 cabbage leaf
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 centaurea microcarpa
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 cherry sweet cherry
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 flax
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 ginkgo biloba leaf
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 ginkgo biloba plant
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 ginkgo biloba pollen
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 grape leaf
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 saffron
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Synonyms:
3,5-dihydroxy-2-(4-hydroxyphenyl)-7-[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxychromen-4-one
 kaempferol 7-O-beta-D-glucopyranoside
 kaempferol-7-O-beta-D-glucopyranoside
 kaempferol-7-O-glucoside
 

Articles:

PubMed:Flavonoids from Algerian endemic Centaurea microcarpa and their chemotaxonomical significance.
PubMed:Improved cryopreservation by diluted vitrification solution with supercooling-facilitating flavonol glycoside.
PubMed:A flavonoid glycoside isolated from Smilax china L. rhizome in vitro anticancer effects on human cancer cell lines.
PubMed:A new lanostane-type triterpenoid from Chamaesyce prostrata.
PubMed:Isolation and purification of four flavonoid constituents from the flowers of Paeonia suffruticosa by high-speed counter-current chromatography.
 
Notes:
None found
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