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2-Methylbenzothiazole

    • Product Name 2-Methylbenzothiazole
    • Alias o-Tolylthiazole
    • Einecs 204-419-1
    • 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

    447790

    Cas Number 615-20-3
    Molecular Formula C8H7NS
    Molecular Weight 149.21 g/mol
    Iupac Name 2-Methyl-1,3-benzothiazole
    Appearance Colorless to pale yellow liquid
    Melting Point −9 °C
    Boiling Point 241-243 °C
    Density 1.133 g/cm³
    Refractive Index 1.624
    Solubility In Water Insoluble
    Flash Point 108 °C (closed cup)
    Structure Benzothiazole ring with a methyl group at position 2

    As an accredited 2-Methylbenzothiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500g amber glass bottle labeled "2-Methylbenzothiazole," featuring hazard symbols, chemical details, batch number, and manufacturer information.
    Shipping 2-Methylbenzothiazole is typically shipped in tightly sealed containers—such as steel or high-density polyethylene drums—to prevent leaks and contamination. It should be stored in a cool, dry, well-ventilated area away from ignition sources. Handling requires chemical-resistant gloves and eye protection. Transport must comply with local and international hazardous materials regulations.
    Storage 2-Methylbenzothiazole should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition. Keep it away from strong oxidizing agents and direct sunlight. Use secondary containment to avoid leaks. Label the container clearly and ensure fire safety measures are in place, as the compound may be combustible.
    Application of 2-Methylbenzothiazole

    Applications of 2-Methylbenzothiazole in Industrial Manufacturing

    As a specialized producer of 2-Methylbenzothiazole, we prioritize real-world performance and compliance in each supported manufacturing segment. Below, we provide detailed application insights across downstream sectors where 2-Methylbenzothiazole is proven to deliver process and product value.

    1. Rubber Vulcanization Accelerator Production

    2-Methylbenzothiazole functions as a key intermediate in the synthesis of rubber vulcanization accelerators such as MBT (2-mercaptobenzothiazole) and its derivatives. In downstream rubber chemical plants, 2-Methylbenzothiazole integrates directly into closed-loop reactor systems under controlled temperature and pressure, where it reacts with sulfur and other agents to form accelerators critical for tire, hose, and gasket manufacturing. Operators select dosage based on rubber grade, targeted cure rate, and specific elastomer base, with QC protocols tightly aligned to accelerator purity extracted from 2-Methylbenzothiazole streams.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • REACH Regulation (EC) No 1907/2006 for substance registration
    • ASTM D4671 – Standard Specification for Accelerators in Vulcanized Rubber
    • Automotive OEM technical delivery conditions (e.g., VW TL501.20 for elastomers)

    Typical usage ratio

    • 0.5–3% of compound formulation by weight, adjusted for target accelerator concentration; precise usage depends on finished product performance parameters

    Downstream process integration

    • Added to closed synthesis reactors for thiazole-type accelerator production; intermediate isolation and purification precedes next-step compounding

    Final product types

    • OEM automotive tires
    • Industrial conveyor belts
    • Rubber gaskets and seals
    • Rubber-coated fabric components

    2. Corrosion Inhibitor Synthesis for Metalworking Fluids

    2-Methylbenzothiazole serves as a critical building block in the manufacture of benzothiazole-based corrosion inhibitors used in formulations for metalworking, engine coolants, and recirculating water systems. Chemical processors introduce the intermediate during active synthesis steps where its aromatic structure facilitates subsequent conversion to thiol or salt forms, which bind selectively to ferrous or non-ferrous substrates, reducing oxidation and pitting in aggressive industrial environments.

    Industry compliance standards

    • OECD Guidelines for Testing of Chemicals (relevant to toxicity, biodegradability)
    • ASTM D6557 – Standard Test Method for Evaluation of Rust Preventatives
    • EU CLP Regulation (EC) No 1272/2008 classification for safe use in coolant and MWF applications
    • ISO 6743-13:2002 for metalworking fluid classification and performance

    Typical usage ratio

    • 0.1–0.5% of inhibitor intermediate batch volume; ratio refined per expected corrosion protection duration and fluid matrix (oil-based vs. water-based)

    Downstream process integration

    • Charged into synthesis reactors for in situ inhibitor functionalization, followed by blending with additive packages for commercial fluid manufacture

    Final product types

    • Industrial engine coolants and antifreezes
    • Metalworking fluid concentrates and semi-synthetics
    • Closed-system water treatment additives
    • Protective rust-inhibiting sprays

    3. Dye Intermediate for Textile and Leather Processing

    Downstream specialty dye manufacturers utilize 2-Methylbenzothiazole as a core intermediate when producing benzothiazole-derived colorants, especially for acid, direct, and sulfur dye classes. The compound’s methyl-substituted benzene ring structure supports robust chromophore formation during controlled sulfonation or diazotization, yielding dye precursors with superior affinity to cellulose, polyamide, and natural leather substrates. Material handling protocols include staged addition, with process controls focused on homogeneity and conversion yield.

    Industry compliance standards

    • GOTS (Global Organic Textile Standard) for permitted dye intermediates
    • ZDHC MRSL 2.0 (Zero Discharge of Hazardous Chemicals)
    • OEKO-TEX® STANDARD 100 restricted substance list
    • ISO 9001:2015 certified dye production facilities

    Typical usage ratio

    • 2–8% of total reaction mixture for dye intermediate synthesis; adjusted based on target dye yield and coloration strength

    Downstream process integration

    • Stepped addition into colorant synthesis reactors; processed via diazotization, sulfonation or condensation prior to purification and milling for dye formulation

    Final product types

    • Reactive, sulfur, and acid textile dyes
    • Leather colorant solutions
    • Industrial inks for fabric and paper
    • Non-woven fiber dye staples

    4. Synthesis of Pharmaceutical Intermediates (API Precursors)

    In pharmaceutical chemical manufacturing, 2-Methylbenzothiazole acts as a specialized intermediate in the multi-step synthesis of active ingredient precursors such as antihypertensives, antifungals, and anti-inflammatory agents. GMP-compliant facilities introduce the raw material during controlled condensation or cyclization steps, with automated dosing aligned to batch record specifications. Adjustments in input proportion correlate with desired product purity and downstream route yield to minimize impurity profiles in regulated APIs.

    Industry compliance standards

    • ICH Q7 – Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211
    • European Pharmacopoeia monographs for intermediates
    • ISO 14001:2015 (for safe handling during synthesis)

    Typical usage ratio

    • 5–15% of initial charge in synthesis step; refined according to target precursor molecular yield and purity required by downstream API pathway

    Downstream process integration

    • Fed into reaction vessels for condensation or cyclization; typically followed by recrystallization, extraction, and assay ahead of API finishing routes

    Final product types

    • API intermediates for cardiovascular drugs
    • Bulk intermediates for antifungal pharmaceuticals
    • Key segments of anti-inflammatory compound synthesis chains
    • Fine chemical intermediates for generic formulations
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