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2-Amino-6-Methylbenzothiazole

    • Product Name 2-Amino-6-Methylbenzothiazole
    • Alias 2-AMBT
    • Einecs 219-020-7
    • 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

    458470

    Cas Number 1193-02-8
    Molecular Formula C8H8N2S
    Molecular Weight 164.23 g/mol
    Appearance Light yellow to beige powder
    Melting Point 147-150 °C
    Solubility In Water Slightly soluble
    Purity Typically >98%
    Storage Conditions Store in a cool, dry place, tightly closed
    Iupac Name 2-amino-6-methyl-1,3-benzothiazole
    Smiles CC1=CC2=C(S1)N=C(N)C=C2

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

    Packing & Storage
    Packing The 100g 2-Amino-6-Methylbenzothiazole comes in a sealed amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 2-Amino-6-Methylbenzothiazole is shipped in tightly sealed containers, protected from moisture and light. It should be labeled appropriately as a chemical substance, handled according to safety protocols to avoid inhalation, ingestion, or skin contact. Transport follows regulatory guidelines for hazardous materials to ensure safe delivery and prevent environmental contamination.
    Storage Store 2-Amino-6-Methylbenzothiazole in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep separated from incompatible substances such as strong oxidizing agents and acids. Clearly label the container, and restrict access to trained personnel. Use secondary containment to prevent spills and ensure compliance with local regulations.
    Application of 2-Amino-6-Methylbenzothiazole

    Applications of 2-Amino-6-Methylbenzothiazole in Industrial Manufacturing

    As a direct manufacturer specializing in the industrial production of 2-Amino-6-Methylbenzothiazole, we support a focused set of application scenarios across established chemical sectors. The following sections outline the principal downstream uses, with each scenario detailing regulatory compliance, recommended formulation ratios, integration points in the production process, and the end product categories.

    1. Synthesis of Sulfur-Containing Pharmaceutical Intermediates

    In the pharmaceutical sector, established process designers employ this molecule to introduce specific thiazole structures during the synthesis of active pharmaceutical intermediates, primarily in antibacterial, antitubercular, and central nervous system drug development lines. Downstream R&D formulates the raw material for coupling reactions, where it contributes its functionalized aromatic system as a key nucleus. The usage ratio is determined in route scouting and process validation, driven by stoichiometry for batch and continuous manufacturing reactors.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopeia (monograph references for intermediates)
    • US FDA 21 CFR Part 211 for drug application intermediates
    • Chinese Pharmacopoeia (Appendix IX for synthesis requirements)

    Typical usage ratio

    • Equimolar to target molecular transformation; typically 0.8%–2.2% w/w based on batch size, adjusted according to yield optimization and process losses

    Downstream process integration

    • Charged into high-shear reactors after main ring-forming step
    • Undergoes nucleophilic aromatic substitution or condensation, followed by purification and crystallization
    • QC on completeness of reaction via HPLC and NMR monitoring

    Final product types

    • Benzothiazole antibiotic precursors
    • Anticonvulsant intermediate compounds
    • Building blocks for anti-tuberculosis APIs
    • Specialty CNS-active pharmaceutical intermediates

    2. Rubber Vulcanization Accelerators

    Compounders in the rubber and elastomer industries employ this material in formulating thiazole-based accelerators, essential for high-performance tire and industrial rubber products. In accelerator manufacturing, it undergoes sulfenamide condensation with other aromatic amines, entering the process before secondary catalyst addition. Usage—calculated by rubber matrix and application requirements—directly influences crosslinking density and mechanical performance.

    Industry compliance standards

    • ISO 9001:2015 for Quality Management
    • ASTM D2084 for Vulcanization Measurement
    • REACH Regulation (EC) No 1907/2006 Annex XVII for rubber chemicals
    • IATF 16949 for automotive elastomers

    Typical usage ratio

    • 0.3%–1.2% by weight of total accelerator package
    • Adjusted according to rubber type and curing cycle speed

    Downstream process integration

    • Dosed into internal mixer or mill at pre-mixing with bulk accelerators
    • Incorporates via melt blending prior to sulfur vulcanization
    • QC by tensile strength, elongation at break, and cure rate index

    Final product types

    • High-durability automotive tire treads
    • Conveyor belt base layers
    • Technical molded industrial seals and gaskets
    • Rubberized anti-vibration pads

    3. Corrosion Inhibitor Synthesis for Industrial Cooling Systems

    Downstream corrosion control chemical manufacturers incorporate the raw material as a ring-based building block in synthesizing benzothiazole-thio derivatives for water treatment. The aromatic amine group forms the core structure in custom inhibitors, tailored for closed-loop cooling and process water. Dosing levels are established during inhibitor blending trials to balance system protection with cost efficiency and environmental safety.

    Industry compliance standards

    • ANSI/AWWA B603-19 for cooling water treatment chemicals
    • ISO 14001:2015 Environmental Management
    • OHSAS 18001 for chemical workplace safety
    • EU Biocidal Products Regulation (BPR, Regulation (EU) 528/2012)

    Typical usage ratio

    • 0.05%–0.15% of final inhibitor concentrate
    • Formulator optimizes based on steel and copper alloy system exposure levels

    Downstream process integration

    • Added during inhibitor synthesis at the condensation reaction stage
    • Followed by extraction, filtration, and stabilization before finished blending
    • QC checkpoint: metal coupon static immersion test

    Final product types

    • Circuit water scale and rust inhibitors
    • Chilled water closed-loop anti-corrosion formulas
    • Power plant cooling tower additive blends
    • Heavy industrial heat exchanger treatment packages

    4. Dye Intermediate for Specialty Organic Pigments

    Producers in the colorant sector employ 2-Amino-6-Methylbenzothiazole as a precursor in multi-step syntheses of sulfur-containing thiazole dyes. The compound enters the diazotization and subsequent coupling stages to provide azo and thiazole-based chromophores. Precise dosing ensures color intensity and compatibility with high-performance plastics, inks, and synthetic fiber coloration.

    Industry compliance standards

    • EN 71-3 for migration of coloring agents in toys
    • REACH Annex XVII restrictions for dyes
    • ISO 9001 for pigment manufacturing quality
    • OEKO-TEX Standard 100 for textile dye safety

    Typical usage ratio

    • 5%–8% based on target pigment batch
    • Tuning according to target shade depth and substrate

    Downstream process integration

    • Charged into diazotization reactor with acid donors
    • Coupled to aromatic substrates or resins pre-precipitation
    • QC by colorimetric analysis and HPLC for byproducts

    Final product types

    • Organic yellow and orange pigments for plastics
    • High fastness textile dyes
    • Printing ink pigment dispersions
    • Color masterbatches for fiber extrusion

    5. Analytical Reagent Production for Laboratory Diagnostics

    Producers of laboratory chemicals use this material in formulating highly sensitive sulfur-heterocycle-based reagents for ion and metal detection assays. During the analytical reagent manufacturing cycle, the raw material acts as a key reactant in condensation reactions, yielding target indicator complexes a laboratory might deploy in trace analysis protocols. Formulation ratios are determined via method validation for signal strength and background reduction.

    Industry compliance standards

    • ISO 17034 for reference material producers
    • ISO/IEC 17025 for test laboratory reagents
    • Good Laboratory Practice (GLP) guidelines
    • US EPA Method 200.7 and Method 6010 for metal analysis

    Typical usage ratio

    • 0.01%–0.05% per finished reagent volume
    • Formulation target: maximize specificity and signal-to-noise

    Downstream process integration

    • Addition to reaction chamber after buffer system set-up
    • Complexation with metals under temperature-controlled conditions
    • Final purification via distillation or crystallization

    Final product types

    • Chelating agents for spectrophotometric metal analysis
    • Color indicator reagents for chemical test kits
    • Analytical standards for laboratory calibration
    • Ready-made wet chemistry diagnostic packs
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