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2,5,6-Trimethylbenzothiazole

    • Product Name 2,5,6-Trimethylbenzothiazole
    • Alias 2,5,6-Trimethylbenzo[d]thiazole
    • Einecs 249-959-9
    • 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

    288360

    Cas Number 34461-28-0
    Molecular Formula C10H11NS
    Molecular Weight 177.27 g/mol
    Appearance Yellow to brown solid
    Melting Point 85-88°C
    Boiling Point Unknown
    Density Unknown
    Solubility In Water Insoluble
    Purity Typically ≥98%
    Synonyms 2,5,6-Trimethyl-1,3-benzothiazole
    Smiles CC1=CC(=C2C(=C1C)SC=N2)C
    Inchi InChI=1S/C10H11NS/c1-6-4-8(2)10-9(5-6)12-3-7(10)11/h4-5H,1-3H3

    As an accredited 2,5,6-Trimethylbenzothiazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical, 2,5,6-Trimethylbenzothiazole (25g), is supplied in a sealed amber glass bottle with a tamper-evident cap.
    Shipping 2,5,6-Trimethylbenzothiazole should be shipped in tightly sealed containers, protected from light and moisture. Ensure compliance with local, national, and international regulations for hazardous chemicals. Use appropriate labeling and packaging to prevent leaks or spills. Handle with care, and transport under controlled temperature conditions if specified by the supplier’s safety data sheet (SDS).
    Storage 2,5,6-Trimethylbenzothiazole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect it from light and moisture. Ensure the storage area is equipped for chemical spills and labeled properly to prevent accidental exposure. Use appropriate personal protective equipment when handling.
    Application of 2,5,6-Trimethylbenzothiazole

    Applications of 2,5,6-Trimethylbenzothiazole in Industrial Manufacturing

    As a manufacturer specializing in 2,5,6-Trimethylbenzothiazole, we deliver this intermediate for established, large-scale processes across several chemical sectors. Below are the precise industrial routes where our material integrates deeply, each tied to real compliance demands, formulation levels, process entry points, and resulting end products.

    1. Rubber Vulcanization Accelerators

    2,5,6-Trimethylbenzothiazole serves as a critical building block in the synthesis of vulcanization accelerators, especially in creating derivatives like MBT-based accelerators for tire-grade and industrial rubber. Leading elastomer producers use it during chemical synthesis steps to enhance crosslinking efficiency, improve mechanical properties, and optimize processing safety margins for high-performance rubber goods. The use must align with end-market requirements for non-blooming, low-toxicity, and regulatory approval in tires and industrial components.

    Industry compliance standards

    • REACH Annex XVII (European market restrictions on certain rubber accelerators)
    • US EPA TSCA compliance
    • ISO 9001:2015 certified production management
    • China GB/T 21861-2008—Rubber Chemicals standard

    Typical usage ratio

    • Intermediary stage synthesis: 1.5–2.8% (w/w) in accelerator manufacture
    • Final rubber compounding: typical equivalency per accelerator derived, usually 0.3–0.8 parts per hundred rubber (phr) of final accelerator in the elastomer mix, depending on blend design for tires, conveyor belts, or hoses

    Downstream process integration

    • Precursor input for MBT (2-mercaptobenzothiazole) synthesis at chemical plant reactor stage
    • Further conversion to secondary and tertiary accelerating compounds before being supplied to rubber mixing facilities
    • Finished accelerator added during internal mixer or banbury stage in rubber compounding

    Final product types

    • Radial and bias tires for automotive and heavy machinery
    • Industrial rubber seals and gaskets
    • Conveyor belts, drive belts, and rubberized rollers

    2. Specialty Dyestuff and Pigment Intermediates

    Certain high-performance organic pigments and dyes rely on 2,5,6-Trimethylbenzothiazole as a key chemical building block, especially within the thiazole-based chromophore system, supporting stringent quality and color stability targets. Advanced textile dye manufacturers implement it in multi-step syntheses to amplify light fastness and chemical resistance. Compliance rests on not only pigment performance but also adherence to regional chemical safety and textile eco-label requirements.

    Industry compliance standards

    • OEKO-TEX Standard 100 (for harmful substances in textile chemicals)
    • EU REACH SVHC declaration for dye intermediates
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals - Manufacturing Restricted Substances List)
    • ISO 9001 for pigment manufacturing sites

    Typical usage ratio

    • Dye intermediate synthesis: 2.0–4.5% of total input mass, adjusted for chromophore strength and yield coefficients
    • In final pigment paste: content varies (trace to 0.7%) based on target shade and application sector

    Downstream process integration

    • Batch or continuous reactor charge during synthesis of benzothiazole-based dye intermediates
    • Stepwise condensation and sulfonation to generate final pigment outputs
    • Dispersion into finished dye or pigment slurries using high-shear mixing

    Final product types

    • Reactive and disperse textile dyes for polyester/cellulose blends
    • High-color-stability printing inks
    • Plastic coloring masterbatches for automotive and consumer products

    3. Photographic and Imaging Chemical Synthesis

    Specialty phototools and industrial imaging sectors use this raw material in the controlled synthesis of sensitizer precursors and stabilizer molecules required for silver halide and other traditional photographic emulsions. The material’s thiazole structure supports chemical stability and enhances photoactive compound shelf life during photographic film and plate coating.

    Industry compliance standards

    • ANSI IT9.9 (Stability of processed photographic images)
    • ISO 18902 (Archival storage and permanence of imaging materials)
    • EU REACH for chemical import and handling during sensitizer manufacture
    • US OSHA 29 CFR 1910.1200 for chemical labeling

    Typical usage ratio

    • Intermediate synthesis step: 1.1–3.6% technical input per batch, depending on the silver complex or dye application strength
    • Finished emulsion: low ppm levels (0.005–0.02%) derived after conversion

    Downstream process integration

    • Input at early- or mid-stage in organic chemical synthesis of photoactive ingredients or stabilizers
    • Post-processing, emulsion component added to gelatin-silver coating solution
    • Quality control checks for residuals before casting on film base

    Final product types

    • Black and white and color photographic films
    • Photographic plates and specialty imaging papers
    • Laboratory diagnostic imaging media

    4. Corrosion Inhibitor Formulations

    The benzothiazole nucleus, with methyl substitutions, grants unique properties in synthesizing advanced corrosion inhibitors, especially those designed for protection of copper and alloyed metals in both open and closed system water treatment. Industrial anti-corrosion product engineers dose it during synthesis runs that require targeted performance in harsh alkaline or brine environments without exceeding regulatory residue thresholds in downstream open-use applications.

    Industry compliance standards

    • ASTM D1384—Corrosion test for engine coolants in glassware
    • US EPA regulations for water system additives
    • EN 15051 (Safety and performance of chemical compounds used in water treatment)
    • ISO 9001:2015 for inhibitor manufacturing QC

    Typical usage ratio

    • Corrosion inhibitor synthesis: 0.5–2.0% of total batch composition, adjusted by polymer matrix and intended system life
    • Finished coolant or inhibitor concentrate: converted ingredients dosed at 50–500 ppm (after downstream synthesis and dilution)

    Downstream process integration

    • Early input to the batch reactor in multi-component azole- or thiazole-based corrosion inhibitor manufacturing
    • Blended into final water treatment chemicals post-filtration and post-neutralization
    • QC and performance validation for inhibitor blends before packaging

    Final product types

    • Engine coolants and heat transfer fluids
    • Industrial closed circuit and open system water inhibitors
    • Copper and brass metalworking fluids

    5. Electronics-Grade Chemical Synthesis for Photolithography

    Advanced semiconductor and PCB fabrication processes exploit the high purity and functional reactivity of 2,5,6-Trimethylbenzothiazole–based intermediates in the preparation of novel photoresist sensitizers and protecting groups. The demands for ultra-low trace impurities, tightly specified chemical steps, and documentation for electronics manufacturing necessitate precision logistics and cleanroom-compatible supply.

    Industry compliance standards

    • IATF 16949 for supplier quality systems (automotive semiconductor sectors)
    • RoHS (Restriction of Hazardous Substances Directive)
    • IEC 62474 material declaration for electronics
    • Internal fab chemical QC standards—semiconductor grade purity/trace metal limits

    Typical usage ratio

    • Intermediate photoresist synthesis: 0.2–1.0% as a structural building block in the scale-up batch
    • In final resist formulation: present only as a fully converted intermediate trace or blocked group, not as raw

    Downstream process integration

    • First-stage reacting agent in small-molecule photoinitiator or mask-protector synthesis
    • Conversion to fully functionalized end compound under GMP or cleanroom conditions, with material handled under nitrogen and filtered submicron standards
    • Integrated into advanced photoresist material blending before final product cartridge filling

    Final product types

    • Photolithographic resists for microelectronics (ICs, MEMS)
    • HDI printed circuit board coatings
    • Specialty coatings for wafer-level chip scale packaging
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