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Euxanthic acid

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Euxanthic acid
Names
IUPAC name (8-Hydroxy-9-oxo-9H-xanthen-2-yl) β-D-glucopyranosiduronic acid
Systematic IUPAC name (2S,3S,4S,5R,6S)-3,4,5-Trihydroxy-6-oxane-2-carboxylic acid
Identifiers
CAS Number
3D model (JSmol)
ChemSpider
PubChem CID
UNII
CompTox Dashboard (EPA)
InChI
  • InChI=1S/C19H16O10/c20-9-2-1-3-11-12(9)13(21)8-6-7(4-5-10(8)28-11)27-19-16(24)14(22)15(23)17(29-19)18(25)26/h1-6,14-17,19-20,22-24H,(H,25,26)/t14-,15-,16+,17-,19+/m0/s1Key: JGIDSJGZGFYYNX-YUAHOQAQSA-N
  • InChI=1/C19H16O10/c20-9-2-1-3-11-12(9)13(21)8-6-7(4-5-10(8)28-11)27-19-16(24)14(22)15(23)17(29-19)18(25)26/h1-6,14-17,19-20,22-24H,(H,25,26)/t14-,15-,16+,17-,19+/m0/s1Key: JGIDSJGZGFYYNX-YUAHOQAQBY
SMILES
  • OC(=O)4O(Oc1ccc2Oc3cccc(O)c3C(=O)c2c1)(O)(O)4O
Properties
Chemical formula C19H16O10
Molar mass 404.327 g·mol
Density 1.737 g/ml
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). checkverify (what is  ?) Infobox references
Chemical compound

Euxanthic acid is a xanthonoid glycoside, a conjugate of the aglycone euxanthone with glucuronic acid. Its magnesium salt is the primary colourant of the pigment Indian Yellow.

References

  1. Katherine Spendel, Dr. M. Scott Goodman, Dr. Rebecca Ploeger and Dr. Aaron Shugar. "Preparation of a Synthetic Indian Yellow" (PDF). SUNY Buffalo. Retrieved July 11, 2018.{{cite web}}: CS1 maint: multiple names: authors list (link)
Types of xanthonoids
Aglycones
Glycosides
Acetylated
Misc.


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