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CasNo: 528-48-3
MF: C15H10O6
Appearance: yellow to brown crystalline powder
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Fisetin is used in biological studies as spleen tyrosine kinase inhibitors for autoimmune inflammation disease. Fisetin has neuroprotective properties.
3,4,2',4'-tetrahydroxy-chalcone
3,7,3',4'-tetrahydroxyflavone
Conditions | Yield |
---|---|
With
sodium carbonate / sodium bicarbonate buffer solution; potassium hydrogen sulfate complex;
In
dichloromethane; acetone;
at 20 ℃;
for 21h;
|
96.7% |
3,3′,4′,7-tetraacetoxyflavone
3,7,3',4'-tetrahydroxyflavone
Conditions | Yield |
---|---|
With
sodium dithionite; water; sodium hydroxide;
In
methanol;
at 20 ℃;
for 4h;
Inert atmosphere;
|
65% |
The CAS number of Fisetin is 528-48-3.
More information of Fisetin 528-48-3 are:
CAS Number |
528-48-3 |
Density |
1.688 g/cm3 |
Melting Point |
330 ºC |
Boiling Point |
599.4 ºC at 760 mmHg |
Flash Point |
233 ºC |
Vapor Pressure |
3.23E-15mmHg at 25°C |
Refractive Index |
1.4413 (estimate) |
HS CODE |
29329990 |
PSA |
111.13000 |
LogP |
2.28240 |
Pka |
6.83±0.40(Predicted) |
Synonyms for Fisetin 528-48-3:Fisetin(6CI);Flavone, 3,3',4',7-tetrahydroxy- (8CI);2-(3,4-Dihydroxyphenyl)-3,7-dihydroxy-4H-benzopyran-4-one;3,3',4',7-Tetrahydroxyflavone;5-Desoxyquercetin;Bois Bleu de Honqrie;C.I.75620;C.I. Natural Brown 1;Cotinin;Fisetholz;Fustel;Fustet;Junger Fustik;NSC 407010;NSC 656275;Superfustel;Superfustel K;Ungarisches Gelbholz;Ventin Sumach;Viset;Young Fustic;Young FusticCrystals;Zante Fustic;
The chemical formula of Fisetin is C15H10O6 which containing 15 Carbon atoms,10 Hydrogen atoms and 6 Oxygen atoms,and the molecular weight of Fisetin is 286.241.
Fisetin, a naturally occurring flavonoid, is a primary reference substance with assigned absolute purity. It is derived from various plant sources and exhibits a range of biological activities, including its role as a spleen tyrosine kinase inhibitor and neuroprotective properties. Fisetin is characterized by its ochre powder appearance and is produced by PhytoLab GmbH & Co. KG.
InChI:InChI=1/C15H10O6/c16-8-2-3-9-12(6-8)21-15(14(20)13(9)19)7-1-4-10(17)11(18)5-7/h1-6,16-18,20H
Relevant articles related to Fisetin:
Article |
Source |
Synthesis of fisetin and 2′,4′,6′-trihydroxydihyrochalcone 4′-O-β-neohesperidoside based on site-selective deacetylation and deoxygenation |
Tsunekawa, Ryuji,Hanaya, Kengo,Higashibayashi, Shuhei,Sugai, Takeshi , p. 1316 - 1322 (2018/07/29) |
MICROBIAL PRODUCTION OF THE FLAVONOIDS GARBANZOL, RESOKAEMPFEROL AND FISETIN |
- Page/Page column 41; 42, (2016/06/01) |
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