3,5-Dihydroxybenzoic acid

From WikiMD's Medical Encyclopedia

Revision as of 06:01, 3 March 2025 by Prab (talk | contribs) (CSV import)
(diff) ← Older revision | Latest revision (diff) | Newer revision → (diff)

3,5-Dihydroxybenzoic acid, also known as α-Resorcylic acid, is a type of dihydroxybenzoic acid with the chemical formula C_7H_6O_4. It is one of the several isomers of dihydroxybenzoic acid, which are distinguished by the positions of the hydroxyl groups on the benzene ring.

Chemical Properties[edit]

3,5-Dihydroxybenzoic acid is a white to off-white crystalline powder. It has a melting point of approximately 230°C and decomposes upon boiling. The compound is slightly soluble in water but more soluble in ethanol and ether.

Synthesis[edit]

The synthesis of 3,5-Dihydroxybenzoic acid can be achieved through various chemical reactions, including the Kolbe-Schmitt reaction and the hydrolysis of suitable precursors.

Applications[edit]

3,5-Dihydroxybenzoic acid is used in the synthesis of various pharmaceuticals, dyes, and polymers. It also serves as an intermediate in organic synthesis and can be used in the study of enzyme activities.

Related Compounds[edit]

See Also[edit]

References[edit]

This article is a stub related to chemistry. You can help WikiMD by expanding it!


Navigation: Wellness - Encyclopedia - Health topics - Disease Index‏‎ - Drugs - World Directory - Gray's Anatomy - Keto diet - Recipes


Ad. Transform your life with W8MD's

GLP-1 weight loss injections special from $29.99 with insurance

Advertise on WikiMD


WikiMD Medical Encyclopedia

Medical Disclaimer: WikiMD is for informational purposes only and is not a substitute for professional medical advice. Content may be inaccurate or outdated and should not be used for diagnosis or treatment. Always consult your healthcare provider for medical decisions. Verify information with trusted sources such as CDC.gov and NIH.gov. By using this site, you agree that WikiMD is not liable for any outcomes related to its content. See full disclaimer.
Credits:Most images are courtesy of Wikimedia commons, and templates, categories Wikipedia, licensed under CC BY SA or similar.