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CHRYSIN | ||
PRODUCT IDENTIFICATION | ||
CAS NO. | 480-40-0 |
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EINECS NO. |
207-549-7 | |
FORMULA | C15H10O4 | |
MOL WT. | 254.24 | |
H.S. CODE |
2932.99.6100 | |
TOXICITY |
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SYNONYMS | 5,7-Dihydroxy-2-phenyl-4H-benzo[b]pyran-4-one; | |
5,7-Dihidroxi-2-fenil-4H-benzo[b]piran-4-ona; 5,7-Dihydroxy-2-phényl-4H-benzo[b]pyranne-4-one; 5,7-Dihydroxyflavone; Galangin flavanone; | ||
SMILES |
c12c(oc(c3ccccc3)cc1=O)cc(O)cc2O | |
CLASSIFICATION |
Flavone | |
EXTRA NOTES |
5,7-Dihydroxyflavone is found in carrot. Chrysin is a naturally occurring flavone chemically extracted from the blue passion flower (Passiflora caerulea). Honeycomb also contains small amounts. It is also reported in Oroxylum indicum or Indian trumpetflower. (Wikipedia) | |
PHYSICAL AND CHEMICAL PROPERTIES | ||
PHYSICAL STATE | yellow powder | |
MELTING POINT | 285 - 286 C | |
BOILING POINT |
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SPECIFIC GRAVITY |
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SOLUBILITY IN WATER | Practically insoluble (84 mg/l) | |
SOLVENT SOLUBILITY |
Soluble in alkali hydroxide solution, slightly soluble in alcohol, chloroform, ether. | |
pH | ||
VAPOR DENSITY |
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REFRACTIVE INDEX |
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NFPA RATINGS |
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AUTOIGNITION |
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FLASH POINT |
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STABILITY | Stable under normal conditions. | |
EXTERNAL LINKS & GENERAL DESCRIPTION | ||
Wikipedia Linking - Chrysin Google Scholar Search - Chrysin Drug Information Portal (U.S. National Library of Medicine) - Chrysin PubChem Compound Summary - Chrysin KEGG (Kyoto Encyclopedia of Genes and Genomes) - Chrysin http://www.ebi.ac.uk/ - Chrysin http://www.ncbi.nlm.nih.gov/ - Chrysin http://toxnet.nlm.nih.gov/ Local | ||
SALES SPECIFICATION | ||
APPEARANCE |
yellow powder | |
ASSAY |
99.0% min | |
WATER |
0.5% max | |
HEAVY METALS |
10ppm max |
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TRANSPORTATION | ||
PACKING | | |
HAZARD CLASS | ||
UN NO. | ||
GENERAL DESCRIPTION OF FLAVONOID |
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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.
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SAFETY INFORMATION | ||
HAZARD OVERVIEW |
May be harmful if inhaled. May cause respiratory tract irritation. May be harmful if absorbed through skin. May cause skin irritation. May cause eye irritation. May be harmful if swallowed. | |
HAZARD CODES |
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RISK PHRASES |
36/37/38 | |
SAFETY PHRASES |
22-24/25 | |
PRICE INFORMATION | ||
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