2,4-Dihydroxybenzoic acid

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2,4-Dihydroxybenzoic acid
Chemical structure of 2,4-dihydroxybenzoic acid
Names
IUPAC name
2,4-dihydroxybenzoic acid
Other names
beta-Resorcylic acid
beta-Resorcinolic acid
p-Hydroxysalicylic acid
2,4-DHBA
Identifiers
89-86-1 YesY
ChEMBL ChEMBL328910 YesY
ChemSpider 1446 YesY
DrugBank DB02839 YesY
Jmol 3D model Interactive image
PubChem 1491
  • InChI=1S/C7H6O4/c8-4-1-2-5(7(10)11)6(9)3-4/h1-3,8-9H,(H,10,11) YesY
    Key: UIAFKZKHHVMJGS-UHFFFAOYSA-N YesY
  • C1=CC(=C(C=C1O)O)C(=O)O
Properties
C7H6O4
Molar mass 154.12 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).
YesY verify (what is YesYN ?)
Infobox references

2,4-Dihydroxybenzoic acid (β-resorcylic acid) is a dihydroxybenzoic acid.

As a resorcylic acid, it is one of the three isomeric crystalline acids that are both carboxyl derivatives of resorcinol and dihydroxy derivatives of benzoic acid.[1]

It is a degradation product of cyanidin glycosides from tart cherries in cell cultures.[2] It is also a metabolite found in human plasma after cranberry juice consumption.[3]

References

  1. Resorcyclic acid on merriam-webster on-line dictionary
  2. Degradation Products of Cyanidin Glycosides from Tart Cherries and Their Bioactivities. Navindra P. Seeram, Leslie D. Bourquin and Muraleedharan G. Nair, J. Agric. Food Chem., 2001, 49 (10), pp. 4924–4929, doi:10.1021/jf0107508
  3. GC-MS Determination of Flavonoids and Phenolic and Benzoic Acids in Human Plasma after Consumption of Cranberry Juice. Kai Zhang and Yuegang Zuo, J. Agric. Food Chem., 2004, 52 (2), pp. 222–227, doi:10.1021/jf035073r

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