Apigenin
| Names | |
|---|---|
| IUPAC name 4′,5,7-Trihydroxyflavone | |
| Systematic IUPAC name 5,7-Dihydroxy-2-(4-hydroxyphenyl)-4H-1-benzopyran-4-one | |
| Other names Apigenine; Chamomile; Apigenol; Spigenin; Versulin; C.I. Natural Yellow 1 | |
| Identifiers | |
| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| DrugBank | |
| ECHA InfoCard | 100.007.540 | 
| EC Number | 
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| KEGG | |
| PubChem CID | |
| UNII | |
| CompTox Dashboard (EPA) | |
| 
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| 
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| Properties | |
| C15H10O5 | |
| Molar mass | 270.240 g·mol−1 | 
| Appearance | Yellow crystalline solid | 
| Melting point | 345 to 350 °C (653 to 662 °F; 618 to 623 K) | 
| UV-vis (λmax) | 267, 296sh, 336 nm in methanol | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Apigenin (4′,5,7-trihydroxyflavone), found in many plants, is a flavone compound that is the aglycone of several naturally occurring glycosides. It is a yellow crystalline solid that has been used to dye wool.
Apigenin is abundant in parsley, celery, celeriac, and chamomile flowers. It occurs in many fruits and vegetables, with the highest concentrations in dried and fresh parsley.