Delphinidin
| Names | |
|---|---|
| IUPAC name 3,3′,4′,5,5′,7-Hexahydroxyflavylium | |
| Systematic IUPAC name 3,5,7-Trihydroxy-2-(3,4,5-trihydroxyphenyl)-1λ4-1-benzopyran-1-ylium | |
| Identifiers | |
| 
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| 3D model (JSmol) | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.007.671 | 
| E number | E163b (colours) | 
| KEGG | |
| PubChem CID | |
| UNII | 
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| CompTox Dashboard (EPA) | |
| 
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| 
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| Properties | |
| C15H11O7+ | |
| Molar mass | 303.24 g/mol | 
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). Infobox references | |
Delphinidin (also delphinidine) is an anthocyanidin, a primary plant pigment, and also an antioxidant. Delphinidin gives blue hues to flowers in the genera Viola and Delphinium. It also gives the blue-red color of the grape variety Cabernet Sauvignon, and can be found in cranberries and Concord grapes as well as pomegranates, and bilberries.
Delphinidin, like nearly all other anthocyanidins, is pH-sensitive, i.e. a natural pH indicator, and changes from blue in basic solution to red in acidic solution.