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| Names | |
|---|---|
| IUPAC name
3,5-Bis(β-D-glucopyranosyloxy)-3′,4′,7-trihydroxyflavylium | |
| Systematic IUPAC name
2-(3,4-Dihydroxyphenyl)-7-hydroxy-3,5-bis{[(2S,3R,4S,5S,6R)-3,4,5-trihydroxy-6-(hydroxymethyl)oxan-2-yl]oxy}-1λ4-benzopyran-1-ylium | |
| Other names
Cyanidin 3,5-O-diglucoside | |
| Identifiers | |
3D model (JSmol) |
|
| 1417221 | |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.018.214 
|
| EC Number |
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| KEGG | |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
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| |
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| Properties | |
| C27H31O16 | |
| Molar mass | 611.52 g/mol (chloride 647 g/mol) |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
| |
Cyanidin-3,5-O-diglucoside, also known as cyanin, is an anthocyanin. It is the 3,5-O-diglucosideofcyanidin.
Cyanin can be found in species of the genus Rhaponticum (Asteraceae).[1]
Cyanin can be found in red wine as well as pomegranate juice according to a study done by Graça Miguel, Susana Dandlen, Dulce Antunes, Alcinda Neves, and Denise Martins in the winter of 2004. Pomegranate juice extracted through centrifugal seed separation has higher amounts of cyanidin-3,5-O-diglucoside than juice extracted by squeezing fruit halves with an electric lemon squeezer.[2]
Cyanidin-3,5-O-diglucosideatPhenol-Explorer.eu
