4-HYDROXYBENZOIC ACID
| '' | |
|---|---|
| Chemical name | |
| Other names | ''p''-Hydroxybenzoic acid ''para''-Hydroxybenzoic acid |
| Chemical formula | |
| Molecular mass | g/mol |
| CAS number | [] |
| Density | g/cm³ |
| Melting point | °C |
| SMILES | |
'4-Hydroxybenzoic acid', or ''p''-hydroxybenzoic acid, is a phenolic derivative of benzoic acid. It is a white crystalline solid that is slightly soluble in water and chloroform, but soluble to extremely soluble in alcohols, ether, and acetone.
4-Hydroxybenzoic acid is primarily known as the basis for the preparation of its esters, known as parabens, which are used as preservatives in cosmetics.
| Contents |
| Production |
| See also |
| References |
| External links |
Production
4-Hydroxybenzoic acid is produced commercially from potassium phenoxide and carbon dioxide in the Kolbe-Schmitt reaction. It can also be produced in the laboratory by heating potassium salicylate with potassium carbonate to 240 °C, followed by treating with acid.[1]
See also
The closely related 2-hydroxybenzoic acid is known as salicylic acid, a precursor to aspirin.
References
1. Organic Syntheses, p-hydroxybenzoic acid, Coll. Vol. 2, p. 341 (1943).
External links
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