| Names | |
|---|---|
| Preferred IUPAC name
3,5-Dihydroxybenzoic acid | |
| Other names
α-Resorcylic acid | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.002.482 |
| EC Number |
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PubChem CID |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties[1] | |
| C7H6O4 | |
| Molar mass | 154.121 g·mol−1 |
| Melting point | 235.3 °C (455.5 °F; 508.4 K) |
| soluble | |
| Solubility in acetone | soluble |
| Solubility in ethanol | very soluble |
| Solubility in diethyl ether | very soluble |
| Acidity (pKa) | 4.04[2] |
| Hazards | |
| GHS labelling: | |
| Warning | |
| H315, H319, H335 | |
| P261, P264, P271, P280, P302+P352, P304+P340, P305+P351+P338, P312, P321, P332+P313, P337+P313, P362, P403+P233, P405, P501 | |
| Related compounds | |
Related compounds |
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Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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3,5-Dihydroxybenzoic acid (α-resorcylic acid) is a dihydroxybenzoic acid. It is a colorless solid.
Preparation and occurrence
It is prepared by disulfonation of benzoic acid followed by hydrolysis of the disulfonate.[3]
It is a metabolite of alkylresorcinols, first identified in human urine and can be quantified in urine and plasma, and may be an alternative, equivalent biomarker of whole grain wheat intake.[4]
References
- ↑ Haynes, William M., ed. (2016). "3". CRC Handbook of Chemistry and Physics (PDF) (97th ed.). CRC Press. p. 190. ISBN 9781498754293.
- ↑ Haynes, William M., ed. (2016). "5". CRC Handbook of Chemistry and Physics (PDF) (97th ed.). CRC Press. p. 91. ISBN 9781498754293.
- ↑ Weston, Arthur W.; Suter, C. M. (1941). "3,5-Dihydroxybenzoic Acid". Org. Synth. 21: 27. doi:10.15227/orgsyn.021.0027.
- ↑ Ross, A.B.; Åman, P.; Kamal-Eldin, A. (2004). "Identification of cereal alkylresorcinol metabolites in human urine—potential biomarkers of wholegrain wheat and rye intake". Journal of Chromatography B. 809 (1): 125–130. doi:10.1016/j.jchromb.2004.06.015. PMID 15282102.
