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3,4-Dimethylthiophenol

    • Product Name 3,4-Dimethylthiophenol
    • Alias 3,4-Dimethylbenzenethiol
    • Einecs 228-695-2
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    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 & Storage
    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.
    Application of 3,4-Dimethylthiophenol

    Applications of 3,4-Dimethylthiophenol in Industrial Manufacturing

    As 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

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA Title 21 CFR Parts 210 & 211
    • European Pharmacopoeia monographs for relevant APIs
    • China GMP (2020 revision)

    Typical usage ratio

    • 2–10 mol% relative to the key intermediate; adjusted per molecular design and impurity targets

    Downstream process integration

    • Introduced post-initial substrate preparation, entering either as a nucleophile or thiol-group donor during the controlled condensation step
    • Subject to in situ monitoring by HPLC or NMR for batchwise yield control

    Final product types

    • Benzothiophene-based kinase inhibitors
    • Cyclic sulfur-containing intermediates for cardiovascular and anti-infective APIs

    2. Agrochemical Production – Synthesis of Select Fungicide Intermediates

    In 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

    • FAO/WHO Specifications (JMPS) for pesticide technical materials
    • EU REACH Registration for agrochemicals
    • ISO 9001:2015-certified QC systems for batch records
    • China Ministry of Agriculture mandatory pesticide standards

    Typical usage ratio

    • 0.8–1.5 weight % of total reactants in sulfur heterocycle synthesis; tuned by targeted yield and downstream formulation activity

    Downstream process integration

    • Charged during closed, temperature-controlled sulfurization stage for thioether or thioketone intermediate manufacture
    • In-process gas-phase capture for odor emissions management

    Final product types

    • Sulfur-containing triazole fungicide actives (technical grade)
    • Benzothiophene fungicide precursors

    3. Advanced Dye Intermediates for Specialty Pigments

    Specialty 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

    • OEKO-TEX® Standard 100 for textile colorants
    • EU REACH Annex XVII (dye substance restrictions)
    • ISO 9001:2015 for colorant production
    • GB/T 21866-2008 (China textile dye standards)

    Typical usage ratio

    • 0.5–2 weight % depending on targeted chromophore substituent ratio

    Downstream process integration

    • Added to diazotization or aryl coupling step before oxidation
    • Batchwise blending to avoid over-sulfonation or color deviation

    Final product types

    • Sulfur dyes for cellulosic textiles
    • Intermediate pigment dispersions for plastics and coatings

    4. Polymer Additive Manufacturing – Thioether-Based Modifier Synthesis

    Within 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

    • ASTM D5630 – Standard Test Method for the Ash Content of Plastics
    • UL 94 Flammability standard (for final product regulatory pathways)
    • ISO 9001:2015 for batch consistency and traceability
    • RoHS Directive (if used in electronics-relevant polymers)

    Typical usage ratio

    • 0.3–1.2 weight % of total polymer blend, set by chain length and mechanical property targeting

    Downstream process integration

    • Pre-polymer masterbatch mixing before high-temperature polymerization
    • In-line viscometry and IR tracking for reaction monitoring

    Final product types

    • Impact-modified polyamides and polyesters
    • Heat-stabilized engineering plastics used in automotive components
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