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Names | |||
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Preferred IUPAC name
2-Sulfanylbenzoic acid
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Other names
2-Mercaptobenzoic acid (no longer recommended)
o-Thiosalicylic acid |
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Identifiers | |||
3D model (JSmol)
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508507 | |||
ChEBI | |||
ChemSpider | |||
ECHA InfoCard | 100.005.187 | ||
EC Number | 205-704-3 | ||
3838 | |||
KEGG | |||
MeSH | 2-Thiosalicylic+acid | ||
PubChem CID
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RTECS number | DH3325000 | ||
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Properties | |||
C7H6O2S | |||
Molar mass | 154.18 g·mol−1 | ||
Appearance | Leaf or needle shaped crystals | ||
Density | 1.49 g cm−3 | ||
Melting point | 162 to 169 °C (324 to 336 °F; 435 to 442 K) | ||
log P | 2.39 | ||
Acidity (pKa) | 3.501 | ||
Hazards | |||
EU classification (DSD) (outdated)
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Xi | ||
R-phrases (outdated) | R36/37/38 | ||
S-phrases (outdated) | S26 | ||
Related compounds | |||
Related compounds
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Salicylic acid |
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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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what is ?) | (|||
Infobox references | |||
Thiosalicylic acid is an organosulfur compound containing carboxyl and sulfhydryl functional groups. Its molecular formula is C6H4(SH)(CO2H). it is a yellow solid that is slightly soluble in water, ethanol and diethyl ether, and alkanes, but more soluble in DMSO.
Thiosalicylic acid is prepared from 2-aminobenzoic acid via diazotization.
Thiosalicylic acid is a precursor to the dyestuff thioindigo. Thiosalicylic acid is also used to make the vaccine preservative thiomersal.
It is a precursor to drug candidates for treatment of atherosclerosis and melanoma.