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5-Bromo-2-Methylbenzothiazole

    • Product Name 5-Bromo-2-Methylbenzothiazole
    • Alias 1-Bromo-6-methylbenzo[d]thiazole
    • Einecs 629-226-5
    • 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

    161309

    Product Name 5-Bromo-2-Methylbenzothiazole
    Cas Number 4639-44-9
    Molecular Formula C8H6BrNS
    Molecular Weight 228.11 g/mol
    Appearance Off-white to light yellow powder
    Melting Point 69-73°C
    Purity Typically ≥98%
    Solubility Slightly soluble in organic solvents
    Density 1.6 g/cm³ (approximate)
    Smiles CC1=NC2=CC(=CC=C2S1)Br

    As an accredited 5-Bromo-2-Methylbenzothiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of 5-Bromo-2-Methylbenzothiazole, tightly sealed with a screw cap, labeled with hazard information.
    Shipping 5-Bromo-2-Methylbenzothiazole is shipped in tightly sealed containers, protected from moisture and light, and kept at ambient or cool temperatures. It is transported following relevant chemical safety regulations, with clear labeling and appropriate documentation. Handling should be by trained personnel using personal protective equipment to ensure safety during transit and delivery.
    Storage 5-Bromo-2-Methylbenzothiazole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. It should be kept away from incompatible substances such as strong oxidizing agents. Appropriate labeling and secure containment are essential to prevent accidental release, and access should be restricted to trained personnel only.
    Application of 5-Bromo-2-Methylbenzothiazole

    Applications of 5-Bromo-2-Methylbenzothiazole in Industrial Manufacturing

    5-Bromo-2-methylbenzothiazole serves as a specialized intermediate in several industrial manufacturing processes. Its chemical structure enables targeted transformations, making it valuable in controlled syntheses for advanced material and pharmaceutical production. Below we detail key application scenarios based on established industry practice.

    1. Pharmaceutical Intermediate for Anti-Infective Drug Synthesis

    Manufacturers use 5-bromo-2-methylbenzothiazole in the synthesis of select benzothiazole-based anti-infective agents, particularly in producing APIs for tuberculosis and parasitic disease treatment. The bromine substituent provides a reactive handle for further functionalization during the multi-step condensation and substitution reactions that define this API class. Our facility operates under validated batch records with full traceability and stringent process controls, enabling consistent integration of this intermediate into the customer’s defined synthetic route as outlined in their DMF submissions. We maintain analytical support to profile all critical impurity thresholds as required by global registration dossiers.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP General Chapters — Residual Solvents and Related Substances
    • EU EudraLex Vol. 4 Part II for chemical API manufacturing
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • 0.15 to 0.35 mol per mol of final API in route step; exact ratio adjusted for route yield and impurity control strategy per customer’s process validation data.

    Downstream process integration

    • Introduced in stage two or three of the multi-step organometallic or nucleophilic substitution protocol for heterocyclic core construction.
    • Input batch identity confirmed by IR/NMR and titration before reaction charging.

    Final product types

    • Benzothiazole-derived anti-infective APIs (e.g., tuberculosis drug precursors)
    • Finished oral or parenteral pharmaceutical formulations containing synthesized APIs
    • Veterinary pharmaceuticals utilizing related core structures
    • Pharmaceutical intermediates for further downstream molecule elaboration

    2. Agrochemical Intermediate for Fungicide Synthesis

    Agrochemical manufacturers incorporate 5-bromo-2-methylbenzothiazole into fungicide production, utilizing its brominated benzothiazole scaffold for selective introduction into triazole or strobilurin classes. Production lines focus on maintaining rapid batch turnovers and impurity profiling as dictated by regulatory residue requirements. Our material undergoes QA testing for halogen content and assists in the formation of active moieties that act on fungal biochemical pathways. Detailed COA and regulatory documentation meet Japanese and EU agrochemical safety requirements.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • ISO 17025 Certified Laboratory Testing for Analytical Parameters
    • Regulation (EC) No 1107/2009 (EU Plant Protection Products Regulation)
    • Japanese Agricultural Chemicals Regulation Law (JACL)

    Typical usage ratio

    • 0.07 to 0.18 mol per mol of fungicidal active; adjusted per synthetic conversion step and target residue levels in formulation.

    Downstream process integration

    • Charged during the active ingredient synthesis step prior to functional group elaboration and final formulation blending and granulation.
    • Material undergoes pre-reaction melt point and halogen analysis per SOP.

    Final product types

    • Systemic fungicidal granules and wettable powders
    • Tank-mix fungicide liquid concentrates
    • Seed treatment actives and seed coating agents
    • Professional crop-protection ready-to-use formulas

    3. Specialty Polymer Additive Precursor

    Within the specialty polymer sector, manufacturers employ 5-bromo-2-methylbenzothiazole as a functional monomer precursor for polymer modification, especially for engineering plastics and elastomers requiring enhanced thermal and electrical properties. This integration typically targets high-performance insulating materials for electronic applications or molded automotive components. Strict batch controls and analytical trace metal limits support the demands of downstream polymer reactor charging. Our process engineering enables controlled blending with other functional comonomers, providing batch-to-batch consistency for customer applications.

    Industry compliance standards

    • REACH Regulation EC 1907/2006 Compliance for Substances in Polymers
    • ISO 9001:2015 Quality Management Systems for Polymer Compounds
    • IEC 60216 and UL 94 Certification Potential for Downstream Compounds
    • RoHS 2011/65/EU for Restricted Substances in Electronics

    Typical usage ratio

    • 0.5% to 2.8% (w/w) relative to co-monomers in resin formulation; adjusted based on targeted polymer functional group loading and final product end-use application.

    Downstream process integration

    • Fed directly into the monomer mix tank for step-growth or chain-growth polymerization, or post-polymerization modification step in continuous process environments.
    • QC sampling for residual monomer completeness post-integration.

    Final product types

    • High-performance electrical insulation polymers
    • Thermally stable automotive plastic parts
    • Conductive and anti-static elastomer compounds
    • Specialty film and coating materials for electronics and sensors

    4. Dye and Pigment Intermediate for Electronic Imaging

    Leading dye and pigment manufacturers use 5-bromo-2-methylbenzothiazole to introduce specific heterocyclic motifs into high-purity, lightfast dye precursors, especially for photoresist layers and electronic imaging colorants. The compound’s controlled reactivity supports sulfonation and coupling reactions for producing pixels and organic electronic circuits. All supply batches are subject to high-resolution chromatographic purity checks, with support documentation for downstream RoHS and REACH safety registration where applicable. Application-specific lot control ensures compatibility in precision colorant synthesis for imaging and microelectronics industries.

    Industry compliance standards

    • ISO 18314-1 Colorimetry for Colorant Measurement
    • RoHS 2011/65/EU for electronic colorant components
    • REACH SVHC Annual Update for Dye Precursors
    • IEC 62471 for Chemical Use in Optical Devices

    Typical usage ratio

    • 0.03 to 0.11 mol per mol of final dye or pigment structure, ratio adjusted per chromophore design and end-use spectral requirements.

    Downstream process integration

    • Charged during primary intermediate coupling for azo or thiazole pigment backbone formation in closed, monitored reactors.
    • Product lots undergo lightfastness and purity QC prior to downstream blending steps.

    Final product types

    • Colorants for OLED and LCD display manufacturing
    • High-performance inkjet ink bases
    • Organic photoresist compounds for semiconductor lithography
    • Industrial digital printing pigment dispersions
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    Email: admin@sinochem-nanjing.com

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