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| Names | |
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| IUPAC name
3′,4′,5,5′-Tetrahydroxy-7-(6-O-{4-[6-O-(4-hydroxybenzoyl)-β-D-glucopyranosyloxy]benzoyl}-β-D-glucopyranosyloxy)-3-[α-L-rhamnopyranosyl-(1→6)-β-D-glucopyranosyloxy]flavylium | |
| Systematic IUPAC name
(12R,13R,14R,15R,16S,42R,43S,44S,45R,46S,82S,83R,84S,85S,86R,142S,143R,144S,145S,146R)-13,14,15,43,44,45,65,83,84,85,143,144,145,184-Tetradecahydroxy-16-methyl-11,17-dioxo-62-(3,4,5-trihydroxyphenyl)-2,5,7,10,13,16-hexaoxa-61λ4-6(3,7)-[1]benzopyrana-1(2),4,8,14(2,6)-tetrakis(oxana)-12(1,4),18(1)-dibenzenaoctadecaphan-61-ylium | |
| Other names
Delphinidin 3-rutinoside-7-O-(6-O-(4-(6-O-(4-hydroxybenzoyl)-beta-D-glucosyl)oxybenzoyl)-beta-D-glucoside) | |
| Identifiers | |
3D model (JSmol) |
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PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |
| C53H59O30+ | |
| Molar mass | 1176.02 g/mol |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Violdelphin is an anthocyanin, a plant pigment, has been found in the purplish blue flower of Aconitum chinense,[1] in the blue flowers in the genus Campanula[2] and in the blue flowers of Delphinium hybridum.[3] It is a flavenoid natural product, incorporating two p-hydroxy benzoic acid residues, one rutinoside and two glucosides associated with a delphinidin.
