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HS Code |
657752 |
| Chemical Name | 3,4-Dimethylthiophenol |
| Molecular Formula | C8H10S |
| Molar Mass | 138.23 g/mol |
| Cas Number | 13706-34-2 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 230-232 °C |
| Density | 1.07 g/cm3 |
| Flash Point | 107 °C |
| Refractive Index | 1.573 |
| Solubility In Water | Insoluble |
| Odor | Strong, unpleasant odor |
| Pka | 7.1 |
| Smiles | CC1=CC(=C(C=C1)S)C |
| Pubchem Cid | 251737 |
As an accredited 3,4-Dimethylthiophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 3,4-Dimethylthiophenol is packaged in a 100 mL amber glass bottle with a secure screw cap, labeled with hazard warnings. |
| Shipping | 3,4-Dimethylthiophenol is shipped in tightly sealed containers made of compatible materials, such as amber glass bottles, to prevent leakage and degradation. The chemical is transported under cool, dry conditions, with clear hazard labeling as it is flammable and emits an unpleasant odor. Handle in compliance with local and international regulations. |
| Storage | 3,4-Dimethylthiophenol should be stored in a tightly sealed container, away from direct sunlight, heat, and sources of ignition. Keep it in a cool, dry, well-ventilated area, separate from strong oxidizers and acids. Properly label the container and avoid contact with incompatible materials. Use in a fume hood and store away from food and drink to prevent contamination. |
Applications of 3,4-Dimethylthiophenol in Industrial ManufacturingAs a specialty chemical producer, we support a range of advanced manufacturing sectors with 3,4-Dimethylthiophenol, targeting applications requiring stringent process integration and product consistency. Below, we outline key real-world downstream use cases, each demonstrating unique sector requirements, compliant formulation practices, established process steps, and specific end products. 1. Pharmaceutical Intermediate Synthesis for Active Pharmaceutical Ingredients (APIs)3,4-Dimethylthiophenol serves as a crucial intermediate in multi-step syntheses of select API sulfur-containing benzothiophene derivatives, where its reactivity with acylation and alkylation agents underpins vital structural assembly. Process reliability hinges on consistent purity and specification adherence for each molecule batch destined for the regulated pharmaceutical market, with manufacturing environments strictly audited for cGMP conformance. Its formulation demands close dosing control based on stoichiometric calculations and the target impurity profile, supporting downstream steps such as condensation, cyclization, and deprotection to achieve the required pharmacological entity. Industry compliance standards
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2. Agrochemical Production – Synthesis of Select Fungicide IntermediatesIn the agrochemical manufacturing chain, 3,4-Dimethylthiophenol is implemented in the synthesis of intermediates for modern fungicides containing sulfur-rich aromatic scaffolds. Process engineers regulate its addition under closed system protocols due to its odor and reactivity, with strict batch documentation for traceable formulation. Dosing relies on reaction yield and impurity monitoring, and integration typically occurs during the sulfurization stage of heterocyclic ring construction, directly impacting biological activity of the final crop protection active ingredient. Industry compliance standards
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3. Advanced Dye Intermediates for Specialty PigmentsSpecialty dye manufacturers employ 3,4-Dimethylthiophenol for its role in synthesizing high-stability sulfurated aromatic intermediates, integral to certain azo and sulfur dyes. Dosing falls under tightly regulated procedures to prevent batchwise color tone drift and maximize target chromophore yield. The raw material is introduced prior to oxidative coupling, forming arylthio linkages that enhance both the photostability and chemical resistance of the final pigment. Quality assurance relies on spectroscopic endpoint determinations, and finished output includes high-purity dye intermediates for further downstream formulation in high-fastness pigment applications. Industry compliance standards
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4. Polymer Additive Manufacturing – Thioether-Based Modifier SynthesisWithin specialty polymer manufacturing, 3,4-Dimethylthiophenol is used for producing thioether-based chain modifiers, which act as crosslinking and stabilization agents in engineering thermoplastics. The incorporation step is essential for controlling polymer flexibility and oxidative resistance. Dosing strategies follow polymer weight percent formulas, with lab-scale optimization to ensure targeted mechanical property shifts. Integration occurs during pre-polymer blending, prior to bulk polymerization, under inert atmosphere to prevent side reactions. The modified polymers are typically used in technical components that demand enhanced ageing and stress-crack resistance. Industry compliance standards
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