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luteone
4H-1-benzopyran-4-one, 3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methyl-2-buten-1-yl)-

Supplier Sponsors

Name:3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)chromen-4-one
CAS Number: 41743-56-0Picture of molecule3D/inchi
FDA UNII: FU3E0232IF
Nikkaji Web:J16.475E
XlogP3-AA:4.20 (est)
Molecular Weight:354.35866000
Formula:C20 H18 O6
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
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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: 635.70 °C. @ 760.00 mm Hg (est)
Flash Point: 448.00 °F. TCC ( 230.90 °C. ) (est)
logP (o/w): 5.080 (est)
Soluble in:
 water, 2.076 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.
Luteone 98%
BOC Sciences
For experimental / research use only.
Luteone >98%
Odor: characteristic
Use: Luteone is a natural flavonoid isolated from the herbs of Erythrina variegata Linn.
Coompo
For experimental / research use only.
Luteone from Plants ≥96%
 
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 luteone usage levels up to:
 not for fragrance use.
 
Recommendation for luteone 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 :5281797
National Institute of Allergy and Infectious Diseases:Data
3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)chromen-4-one
Chemidplus:0041743560
 
References:
 3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)chromen-4-one
NIST Chemistry WebBook:Search Inchi
Pubchem (cid):5281797
Pubchem (sid):135230730
 
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):C10498
HMDB (The Human Metabolome Database):HMDB36595
FooDB:FDB015507
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 black bean plant
Search Trop Picture
 bean butter bean
Search Trop Picture
 bean field bean plant
Search Trop Picture
 lupine white lupine
Search Trop Picture
 
Synonyms:
4H-1-benzopyran-4-one, 3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methyl-2-buten-1-yl)-
4H-1-benzopyran-4-one, 3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methyl-2-butenyl)-
3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methyl-2-buten-1-yl)-4H-chromen-4-one
3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methyl-2-butenyl)-4H-1-benzopyran-4-one
3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)chromen-4-one
 ruizgenin
 uncinanone A
 

Articles:

PubMed:Antimicrobial and antioxidant activity and chemical characterisation of Erythrina stricta Roxb. (Fabaceae).
PubMed:LC-MSMS profiling of flavonoid conjugates in wild Mexican lupine, Lupinus reflexus.
PubMed:Sucrose-induced lupine defense against Fusarium oxysporum. Sucrose-stimulated accumulation of isoflavonoids as a defense response of lupine to Fusarium oxysporum.
PubMed:Regioselective synthesis of 6-alkyl- and 6-prenylpolyhydroxyisoflavones and 6-alkylcoumaronochromone derivatives.
PubMed:Investigations of Terpenoid Biosynthesis by the Dorid Nudibranch Cadlina luteomarginata.
PubMed:Distribution of isoflavones in lupin hypocotyls. Possible control of cell wall peroxidase activity involved in lignification.
 
Notes:
Constit. of Lupinus spp.
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