Digallic acid

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Digallic acid
200px
meta-depside bond digalloyl ester
Names
IUPAC name
3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyl)oxybenzoic acid
Other names
Digallate
3,4-dihydroxy-5-(3,4,5-trihydroxybenzoyloxy)benzoate
m-digallic acid
Digalloyl ester
Identifiers
536-08-3 YesY
ChEMBL ChEMBL366356 N
ChemSpider 334 N
Jmol 3D model Interactive image
Interactive image
PubChem 341
  • InChI=1S/C14H10O9/c15-7-2-6(3-8(16)11(7)18)14(22)23-10-4-5(13(20)21)1-9(17)12(10)19/h1-4,15-19H,(H,20,21) N
    Key: COVFEVWNJUOYRL-UHFFFAOYSA-N N
  • InChI=1/C14H10O9/c15-7-2-6(3-8(16)11(7)18)14(22)23-10-4-5(13(20)21)1-9(17)12(10)19/h1-4,15-19H,(H,20,21)
    Key: COVFEVWNJUOYRL-UHFFFAOYAG
  • C1=C(C=C(C(=C1O)O)O)C(=O)OC2=CC(=CC(=C2O)O)C(=O)[O-]
  • O=C(O)c2cc(O)c(O)c(OC(=O)c1cc(O)c(O)c(O)c1)c2
Properties
C14H10O9
Molar mass 322.22 g/mol
Vapor pressure {{{value}}}
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N verify (what is YesYN ?)
Infobox references

Digallic acid is a polyphenolic compound found in Pistacia lentiscus.[1] Digallic acid is also present in the molecule of tannic acid.[2] Digalloyl esters involve either -meta or -para depside bonds.[3]

Tannase is an enzyme that uses digallate to produce gallic acid. This enzyme can also be used to produce digallic acid from gallotannins.[4]

References

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  2. Lua error in package.lua at line 80: module 'strict' not found.
  3. Tannin chemistry, by Ann E. Hagerman
  4. Lua error in package.lua at line 80: module 'strict' not found.


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