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HS Code |
589232 |
| Cas Number | 3446-89-7 |
| Molecular Formula | C8H10S |
| Molecular Weight | 138.23 g/mol |
| Synonyms | p-Tolylmethyl mercaptan, 4-Methylbenzyl thiol |
| Appearance | Colorless to pale yellow liquid |
| Odor | Strong, unpleasant, mercaptan-like |
| Boiling Point | 237-239°C |
| Melting Point | -13°C |
| Density | 1.062 g/cm³ at 25°C |
| Flash Point | 100°C (closed cup) |
| Refractive Index | 1.565 at 20°C |
| Solubility In Water | Insoluble |
| Storage Temperature | Store at room temperature, tightly closed |
As an accredited 4-Methylbenzyl Mercaptan factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 4-Methylbenzyl Mercaptan is packaged in a 100 mL amber glass bottle, tightly sealed with a screw cap and hazard labels. |
| Shipping | 4-Methylbenzyl Mercaptan is typically shipped in sealed, chemical-resistant containers to prevent leaks and exposure. It should be transported in compliance with applicable regulations for hazardous materials, kept away from heat, flames, and strong oxidizers, and clearly labeled for safe handling. Ensure cool, well-ventilated storage during transit. |
| Storage | 4-Methylbenzyl mercaptan should be stored in a tightly closed container, away from sources of ignition and heat, in a well-ventilated, cool, and dry area. Protect from direct sunlight, moisture, and incompatible substances such as strong oxidizing agents. Store in a chemical storage cabinet designed for flammable or toxic materials. Clearly label and limit access to authorized, trained personnel only. |
Applications of 4-Methylbenzyl Mercaptan in Industrial Manufacturing4-Methylbenzyl Mercaptan is a specialized aromatic thiol with a distinct reactive profile. Our direct manufacturing supports a range of industrial consumers in need of established sulfur-based intermediates. See below for verified application scenarios, relevant standards, process insights, and finished product examples. 1. Aroma Chemicals for Flavors and FragrancesMany leading fragrance compounders utilize 4-Methylbenzyl Mercaptan to create complex musk, roasted, and savory notes. Its use offers unique thioether profiles in compounding, and direct addition supports the construction of aroma molecules in both liquid and solid phase perfume and flavor matrices. Process technicians must ensure standard compliance and manage sulfur content to avoid off-notes, requiring tight compound QC. Industry compliance standards
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2. Pharmaceutical Synthesis Intermediate4-Methylbenzyl Mercaptan functions as a critical building block in the multistep synthesis of certain active pharmaceutical ingredients, especially in sulfenylation or thioetherification reactions. Our chemical supports GMP-driven processes where controlled sulfur introduction is required, and where API manufacturers demand high-purity material, full traceability, and documentation for clinical batch records. Industry compliance standards
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3. Agrochemical Synthesis Building BlockIntegrators in the crop protection industry use this mercaptan as a key feedstock for the production of sulfur-bearing pesticides, herbicide intermediates, and fungicides. With correct dosing precision, the mercaptan enters multiple routes towards final actives, especially in the formation of thioether linkages or substitution patterns needed for crop efficacy and environmental safety assessment. Industry compliance standards
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4. Rubber and Polymer Chemical ModificationRubber compounders and plastic additive suppliers add 4-Methylbenzyl Mercaptan to enhance crosslinking in vulcanization and introduce aromatic thioether groups into polymer chains. Plants use it to adjust polymer structure and performance, influencing tear resistance, elasticity, and aging characteristics, with quantification of residual sulfur vital for approvals in automotive and general industry. Industry compliance standards
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5. Specialty Chemical Synthesis for ElectronicsManufacturers of electronic-grade chemicals employ 4-Methylbenzyl Mercaptan for the targeted introduction of sulfur atoms into organic dielectric materials and in the fabrication of high-purity intermediates for photoresists. Its aromatic thiol structure supports strong adhesion on gold or silver contacts, enhancing microcircuit reliability and photo-patterning precision for integrated circuit production. Industry compliance standards
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