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Thio Salicylic Acid is a high-purity organosulfur compound supplied by Sarchem Labs for research and industrial applications. It is widely used as an intermediate in pharmaceutical synthesis, agrochemical formulations, and specialty chemical production. Known for its consistent quality and controlled specifications, this compound ensures reliable performance in laboratory and manufacturing processes. Sarchem Labs maintains strict quality standards to deliver dependable and application-ready materials.
Synonym: thiosalicylic acid, 2-mercaptobenzoic acid, o-mercaptobenzoic acid, 2-thiosalicylic acid, o-thiosalicylic acid, 2-carboxythiophenol, o-benzoic acid thiol, o-carboxythiophenol, o-sulfhydrylbenzoic acid, benzoic acid, 2-mercapto
| Appearance | White to off-white / pale yellow crystalline powder |
| Melting Point | 164–169 °C (clear melt) |
| pH of Liquid, Typical (10% soln) | Not routinely specified for solid thiosalicylic acid; estimated acidic solution pH around ~2-3 due to benzoic acid moiety |
| Specific Gravity Approx | ~1.49 g/cm³ (solid density) |
| Odor | Slight sulfur / stench odour typical of thiols |
| Color | White to yellow / off-white |
| Linear Formula | HSC₆H₄CO₂H |
| IUPAC Name | 2-sulfanylbenzoic acid |
| Formula Weight | 154.18–154.19 g/mol |
| percent purity | Typical high purity ~98% |
| Physical Form | Crystalline powder / solid crystals |
| Chemical Name or Material | Thiosalicylic Acid (o-mercaptobenzoic acid) |
| Content / Assay Percent Range | Typically ≥97.5–102.5% (Argentometric titration) ~98% Purity grade |
Classification of the substance or mixture
GHS Label elements, including precautionary statements
Hazards not otherwise classified (HNOC) or not covered by GHS
Yes
GHS Classification in accordance with 29 CFR 1910 (OSHA HCS). For the full text of the H-Statements mentioned in this Section, see Section 16.
Yes
Signal word :
Warning
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Thio salicylic acid is an organosulfur compound derived from salicylic acid. It is valued in pharmaceuticals, chemical synthesis, and research for its unique sulfur-containing structure and versatile reactivity.
Common thio salicylic acid uses include manufacturing pharmaceuticals, corrosion inhibitors, and chemical intermediates. It also appears in certain cosmetic formulations and laboratory research due to its functional chemical groups.
Key thio salicylic acid properties include its sulfur-containing thiol group, ability to chelate metals, and moderate solubility in organic solvents. These features make it valuable in metal complexation and specialized chemical reactions.
Thio salicylic acid is typically prepared by introducing a thiol group into salicylic acid through controlled chemical reactions. The process may involve substitution or coupling steps, followed by purification to ensure high purity.
Handling thio salicylic acid requires gloves, protective eyewear, and adequate ventilation. It may cause skin or eye irritation, so following laboratory safety protocols is essential to prevent health hazards during use.
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