|
FISETIN | ||
PRODUCT IDENTIFICATION | ||
CAS NO. | 528-48-3 |
|
EINECS NO. | 208-434-4 | |
FORMULA | C15H10O6 | |
MOL WT. | 286.24 | |
H.S. CODE |
||
TOXICITY |
||
SYNONYMS |
Fisetin; Fietin; Viset; C.I. Natural Brown 1; C.I. 75620; | |
2-(3,4-Dihydroxyphenyl)-3,7-dihydroxy-4H-1-benzopyran-4-one; 3,3',4',7-Tetrahydroxyflavone; 5-Desoxyquercetin; Cotinin; Fustel; Fustet; 5-Desoxyquercetin; 2-(3,4-Dihydroxyphenyl)-3,7- dihydroxy-chromen-4-one; | ||
SMILES |
c1(c2cc(c(O)cc2)O)oc2c(ccc(c2)O)c(c1O)=O | |
CLASSIFICATION |
Flavonol, Topoisomerase inhibitor, Catechol | |
EXTRA NOTES |
Fisetin is a flavonol, a structurally distinct chemical substance that belongs to the flavonoid group of polyphenols. It can be found in many plants, where it serves as a colouring agent. Its chemical formula was first described by Austrian chemist Josef Herzig in 1891 (Wikipedia) | |
PHYSICAL AND CHEMICAL PROPERTIES | ||
PHYSICAL STATE |
yellow to brown crystalline powder | |
MELTING POINT |
330 C | |
BOILING POINT |
| |
SPECIFIC GRAVITY |
| |
SOLUBILITY IN WATER | ||
pH | ||
VAPOR DENSITY |
| |
REFRACTIVE INDEX |
| |
NFPA RATINGS |
||
AUTOIGNITION |
| |
FLASH POINT |
| |
STABILITY | Stable under normal conditions. | |
EXTERNAL LINKS & GENERAL DESCRIPTION | ||
Wikipedia Linking - Fisetin Google Scholar Search - Fisetin Drug Information Portal (U.S. National Library of Medicine) - Fisetin PubChem Compound Summary - Fisetin KEGG (Kyoto Encyclopedia of Genes and Genomes) - Fisetin Chemical Entities of Biological Interest (ChEBI) - Fisetin http://www.ncbi.nlm.nih.gov/ - Fisetin http://toxnet.nlm.nih.gov/ Local | ||
SALES SPECIFICATION | ||
APPEARANCE |
yellow to brown crystalline powder | |
IDENTIFICATION |
passes Test IR | |
ASSAY |
98% min (HPLC) | |
ASH |
0.5% max | |
LOSS ON DRYING |
3.0% max | |
HEAVY METALS |
10ppm max | |
TRANSPORTATION | ||
PACKING | | |
HAZARD CLASS | ||
UN NO. | ||
OTHER INFORMATION | ||
Hazard Symbols: , Risk Phrases: 36/37/38, Safety Phrases: 26-36 | ||
GENERAL DESCRIPTION OF FLAVONOID | ||
Flavonoid is any member of a class of widely distributed biological natural products containing aromatic heterocyclic skeleton of flavan (2-Phenylbenzopyran) but no nitrogen in plants. Generally, flavonoids are biological pigments providing colours from red to blue in flowers, fruit and leaves. Besides their coloring in plants, flavonoids have important roles in the growth and development of plants; protection against UV-B radiation; forming antifungal barriers; antimicrobial, insecticidal and oestrogenic activities; plant reproduction. Flavonoids also exhibit a wide range of biological properties including anti-microbial, insecticidal and oestrogenic activities. Flavonoids are usually classified into main 6 subgroups as below plus flavans, neoflavonoids, flavonols, aurons, catechins according to the structural patterns.
|
||
PRICE INFORMATION |
||
|
|