luteone
4H-1-benzopyran-4-one, 3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methyl-2-buten-1-yl)-
Identification
| Name | luteone |
| IUPAC | 3-(2,4-dihydroxyphenyl)-5,7-dihydroxy-6-(3-methylbut-2-enyl)chromen-4-one |
| CAS Number | 41743-56-0 |
| FDA UNII | FU3E0232IF |
| Molecular Formula | C20 H18 O6 |
| Molecular Weight | 354.35866000 |
| Nikkaji Number | J16.475E |
Regulatory
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) |
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 luteone usage levels up to | not for fragrance use. |
| Recommendation for luteone flavor usage levels up to | not for flavor use. |
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Potential Uses
Natural Occurrence
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
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.