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Tricetinidin

From Wikipedia, the free encyclopedia
Tricetinidin (chloride)
Names
IUPAC name
5-(5,7-dihydroxychromenylium-2-yl)benzene-1,2,3-triol chloride
Identifiers
3D model (JSmol)
ChEBI
ChemSpider
UNII
  • InChI=1S/C15H10O6/c16-8-5-10(17)9-1-2-13(21-14(9)6-8)7-3-11(18)15(20)12(19)4-7/h1-6H,(H4-,16,17,18,19,20)/p+1
    Key: CMPNIWQMRYYTMK-UHFFFAOYSA-O
  • chloride: InChI=1S/C15H10O6.ClH/c16-8-5-10(17)9-1-2-13(21-14(9)6-8)7-3-11(18)15(20)12(19)4-7;/h1-6H,(H4-,16,17,18,19,20);1H
    Key: MSRWCRMKQPGZND-UHFFFAOYSA-N
  • C1=CC(=[O+]C2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O
  • chloride: C1=CC(=[O+]C2=CC(=CC(=C21)O)O)C3=CC(=C(C(=C3)O)O)O.[Cl-]
Properties
C15H11O6+ (Cl)
Molar mass 287.24 g/mol (cation), 322.69 g/mol (chloride)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Tricetinidin is an intense red-colored chemical compound belonging to the 3-deoxyanthocyanidins. It can be found in black tea infusions.[1] Tricetinidin, in tea, would be a product of the oxidative degallation of epigallocatechin gallate (EGCG).[2]

References

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