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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 | 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. |
Applications of 2-Amino-6-Methylbenzothiazole in Industrial ManufacturingAs 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 IntermediatesIn 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
Typical usage ratio
Downstream process integration
Final product types
2. Rubber Vulcanization AcceleratorsCompounders 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
Typical usage ratio
Downstream process integration
Final product types
3. Corrosion Inhibitor Synthesis for Industrial Cooling SystemsDownstream 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
Typical usage ratio
Downstream process integration
Final product types
4. Dye Intermediate for Specialty Organic PigmentsProducers 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
Typical usage ratio
Downstream process integration
Final product types
5. Analytical Reagent Production for Laboratory DiagnosticsProducers 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
Typical usage ratio
Downstream process integration
Final product types
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