Hexahydroxydiphenic acid
Chemical structure of hexahydroxydiphenic acid
Names
Preferred IUPAC name
4,4′,5,5′,6,6′-Hexahydroxy[1,1′-biphenyl]-2,2′-dicarboxylic acid
Other names
HHDP
3,4,5,3′,4′,5′-Hexahydroxydiphenate
3,4,5,3′,4′,5′-Hexahydroxydiphenic acid
Identifiers
3D model (JSmol)
ChemSpider
  • InChI=1S/C14H10O10/c15-5-1-3(13(21)22)7(11(19)9(5)17)8-4(14(23)24)2-6(16)10(18)12(8)20/h1-2,15-20H,(H,21,22)(H,23,24) ☒N
    Key: MFTSECOLKFLUSD-UHFFFAOYSA-N ☒N
  • InChI=1/C14H10O10/c15-5-1-3(13(21)22)7(11(19)9(5)17)8-4(14(23)24)2-6(16)10(18)12(8)20/h1-2,15-20H,(H,21,22)(H,23,24)
    Key: MFTSECOLKFLUSD-UHFFFAOYAZ
  • O=C(O)c2cc(O)c(O)c(O)c2c1c(O)c(O)c(O)cc1C(=O)O
Properties
C14H10O10
Molar mass 338.224 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Infobox references

Hexahydroxydiphenic acid is an organic compound with the formula [(HO)3C6HCO2H]2. It is the oxidatively coupled derivative of gallic acid[2] It is a white solid, although samples are typically brown owing to oxidation.

Ellagic acid.

Hexahydroxydiphenic acid is a component of some ellagitannins,[3] such as casuarictin. Luteic acid is the monolactone and ellagic acid is the dilactone of hexahydroxydiphenic acid.

See also

References

  1. ↑ "MetaCyc hexahydroxydiphenic acid". biocyc.org.
  2. ↑ Haslam, E.; Cai, Y. (1994). "Plant polyphenols (vegetable tannins): Gallic acid metabolism". Natural Product Reports. 11 (1): 41–66. doi:10.1039/NP9941100041. PMID 15206456.
  3. ↑ Feldman, Ken S.; Iyer, Malliga R.; Liu, Yanze (2003). "Ellagitannin Chemistry. Studies on the Stability and Reactivity of 2,4-HHDP-Containing Glucopyranose Systems". The Journal of Organic Chemistry. 68 (19): 7433–7438. doi:10.1021/jo034495x. PMID 12968897.
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