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7-Chloro-2H-1,4-Benzothiazin-3(4H)-One

    • Product Name 7-Chloro-2H-1,4-Benzothiazin-3(4H)-One
    • Alias Chlorothiazone
    • Einecs 621-327-7
    • 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

    323116

    Chemical Name 7-Chloro-2H-1,4-Benzothiazin-3(4H)-One
    Molecular Formula C8H4ClNOS
    Molecular Weight 197.64 g/mol
    Cas Number 3562-84-3
    Appearance White to light yellow crystalline powder
    Melting Point 177-181°C
    Solubility Slightly soluble in water; soluble in organic solvents like DMSO
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep tightly closed
    Smiles Clc1ccc2c(=O)sncc2c1
    Inchi InChI=1S/C8H4ClNOS/c9-5-1-2-6-7(3-5)11-4-8(12)10-6/h1-4H

    As an accredited 7-Chloro-2H-1,4-Benzothiazin-3(4H)-One 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 7-Chloro-2H-1,4-Benzothiazin-3(4H)-One; labeled with hazard information and product details.
    Shipping 7-Chloro-2H-1,4-Benzothiazin-3(4H)-One is shipped in sealed, chemical-resistant containers to prevent moisture and contamination. It is handled according to standard chemical safety protocols, with careful packaging to avoid breakage during transit. Shipping complies with relevant local and international regulations for chemical transport, ensuring secure and reliable delivery.
    Storage Store 7-Chloro-2H-1,4-benzothiazin-3(4H)-one in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area, away from sources of ignition, incompatible substances, and strong oxidizers. Ensure the storage area is equipped with proper chemical safety measures and is accessible only to trained personnel. Label containers clearly and handle using appropriate protective equipment.
    Application of 7-Chloro-2H-1,4-Benzothiazin-3(4H)-One

    Applications of 7-Chloro-2H-1,4-Benzothiazin-3(4H)-One in Industrial Manufacturing

    We supply 7-Chloro-2H-1,4-Benzothiazin-3(4H)-One strictly for authentic industrial applications based on decade-long production experience and close collaborations with demanding B2B customers. All listed scenarios reflect real, established downstream processes where our material integrates efficiently under controlled, auditable conditions. Our technical support spans the entire process from raw material handling to customer QC release to ensure traceability and performance in every batch.

    1. Anti-Tuberculosis Pharmaceutical Ingredient Synthesis

    Pharmaceutical manufacturers employ this benzothiazine derivative as a core intermediate in the synthesis of rifapentine and related rifamycin antibiotics. Integration occurs at the condensation step, allowing for efficient ring formation without introducing extraneous impurities. Sourcing from established GMP producers ensures endpoint bioactivity and regulatory acceptability for active tuberculosis drugs. Quality release includes verification by HPLC impurity profiling, in accordance with stringent pharmacopoeia limits.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • China Pharmacopoeia ChP 2025 (API intermediate sections)
    • European Pharmacopoeia (Ph. Eur. 11.0), applicable intermediate guidelines
    • US FDA 21 CFR Part 210/211 (where applicable for supply to US pharma)

    Typical usage ratio

    • Batch ratios range from 0.98 to 1.02 molar equivalents relative to precursor aldehydes, adjusted based on purity and conversion yield requirements

    Downstream process integration

    • Added during the cyclization and coupling stage with hydrazine derivatives in rifapentine API synthesis routes
    • Tight impurity control required prior to final API crystallization

    Final product types

    • Rifapentine API
    • Bulk antibiotic intermediates for finished oral tablets and injectable formulations

    2. Intermediate for Agrochemical Synthesis

    Agrochemical producers utilize this compound as a sulfur-heterocycle building block in the production of selected fungicide actives. It reacts efficiently in stepwise N-alkylation or acylation, contributing to fungicidal spectrum targeting phytopathogenic fungi in cereals and vegetables. Process engineers implement precise temperature and solvent controls to minimize side-reactions, facilitating compliance with regulatory impurity thresholds for downstream crop protection agents.

    Industry compliance standards

    • FAO/WHO Specifications for Pesticides
    • SANCO/12545/2014 guidance on technical active substance purity (EU)
    • China ICAMA technical material registration requirements
    • REACH Annex VII–IX registration dossiers (as supporting intermediate, if exported to EU)

    Typical usage ratio

    • Dosage typically at stoichiometric levels: 1.00–1.05 molar equivalents per target molecule, variable upon desired fungicide yield and process scale

    Downstream process integration

    • Enters reaction vessel post-initial condensation, prior to functional group derivatization or sulfonation
    • In-line HPLC assays monitor isolation purity prior to further synthesis steps

    Final product types

    • Technical-grade fungicide actives containing thiazinone core
    • Wettable powders and emulsifiable concentrate crop protection agents

    3. Dye and Pigment Intermediate for Specialty Colorants

    Specialty pigment and dye manufacturers introduce this heterocyclic scaffold during azo and sulfur dye synthetic pathways, particularly in the batch production of heat-resistant paints and electronic-grade printing inks. Its chemical structure provides chromophoric stability and enhances thermal performance. Advanced analytical controls during the diazotization stage maintain batch-to-batch consistency, supporting downstream integration in automotive and industrial coatings.

    Industry compliance standards

    • ISO 9001:2015 for quality management in pigment manufacturing
    • EN 71–3 (Safety of toys – migration of specific elements) when pigments are used for toy applications
    • RoHS Directive 2011/65/EU (limitation on certain hazardous substances in electrical and electronic equipment)
    • SGS colorant and additives material traceability guidelines

    Typical usage ratio

    • Composition typically calls for 0.1–0.3 parts per 10 parts dye base, modulated by the targeted shade intensity and heat stability requirements

    Downstream process integration

    • Added at the colorant formation stage before coupling with diazo components
    • Color yield and fastness adjusted by real-time spectrophotometry

    Final product types

    • High-performance specialty dyes for plastics
    • Industrial-grade pigments used in automotive and heat-cured paints
    • Precision printing inks for PCBs and electronics

    4. Intermediate for Advanced Material Synthesis (Polymer Additives)

    Producers of specialty polymers occasionally require stabilized heterocyclic building blocks to impart thermal or UV resistance to select engineering plastics. The compound is effective as a precursor for synthesizing benzothiazine-based stabilizers incorporated into masterbatch formulations. The integration process demands strict moisture and color control, as even trace impurity or residual moisture impacts downstream polymer performance. End-use testing focuses on accelerated aging and mechanical strength under UV exposure.

    Industry compliance standards

    • ISO 14001 for environmental management in advanced polymer production
    • ASTM D638/D790 for mechanical and UV performance of finished plastics
    • GB/T 2408 for flame retardancy in plastic components (for electronics)
    • UL 746C (Polymer Additive Safety, if used in US electrical/electronics)

    Typical usage ratio

    • Typical inclusion level is 0.05–0.15 wt% in masterbatch, dependent on base polymer reactivity and stability target

    Downstream process integration

    • Introduced during early masterbatch compounding, blended with base resin under nitrogen to prevent oxidation
    • Controlled melt extrusion parameters to ensure uniform dispersal with minimum color shift

    Final product types

    • Engineering polymer masterbatches with built-in UV or thermal stabilizers
    • High-durability plastic components for automotive, appliance, and outdoor applications
    Free Quote

    Competitive 7-Chloro-2H-1,4-Benzothiazin-3(4H)-One prices that fit your budget—flexible terms and customized quotes for every order.

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