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6-Bromo-2-Benzothiazolinone

    • Product Name 6-Bromo-2-Benzothiazolinone
    • Alias 6-Bromo-2(3H)-benzothiazolone
    • Einecs 221-139-7
    • 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

    288023

    Product Name 6-Bromo-2-Benzothiazolinone
    Cas Number 15552-91-7
    Molecular Formula C7H4BrNOS
    Molecular Weight 230.08 g/mol
    Appearance Light yellow to beige crystalline powder
    Melting Point 177-181°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents like DMSO and ethanol
    Boiling Point No data available (decomposes before boiling)
    Storage Conditions Store at 2-8°C, protected from light and moisture

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

    Packing & Storage
    Packing The 6-Bromo-2-Benzothiazolinone is supplied in a sealed 25g amber glass bottle with a secure screw cap and hazard labeling.
    Shipping 6-Bromo-2-Benzothiazolinone is shipped in tightly sealed containers, protected from moisture and light. It is classified as a laboratory chemical and may require handling as a hazardous substance under applicable regulations. Appropriate labeling and documentation are provided, and shipping follows all relevant safety guidelines for chemical transport, including temperature control if necessary.
    Storage 6-Bromo-2-Benzothiazolinone should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition, moisture, and incompatible substances such as strong oxidizers. Protect from direct sunlight and keep at room temperature. Ensure proper labeling and secure storage to prevent unauthorized access. Use appropriate personal protective equipment when handling the chemical.
    Application of 6-Bromo-2-Benzothiazolinone

    Applications of 6-Bromo-2-Benzothiazolinone in Industrial Manufacturing

    As a specialized manufacturer of 6-Bromo-2-Benzothiazolinone, we supply this advanced organic intermediate to key industrial sectors with established downstream demand. Our quality management and technical team support precise integration into critical formulation and synthesis workflows, strictly targeting proven end-use markets and observing specific compliance frameworks at each stage.

    1. Pharmaceutical Intermediate Synthesis for Cephalosporin Antibiotics

    6-Bromo-2-Benzothiazolinone serves as a critical coupling building block in the synthesis of cephalosporin intermediates, specifically in the construction of side chain heterocycles. Its consistent specification and impurity control are essential in large-scale production of semi-synthetic antibiotic actives. Our regular customers use it in multi-step reactions, introducing it at the heterocycle ring formation stage where precise bromination patterns define the bioactivity of the final product. Compliance with pharmacopoeial guidance and validated process audits are standard practice for all shipments into these facilities.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, ICH Q7)
    • European Pharmacopoeia (Ph. Eur.) requirements for intermediates
    • US Food and Drug Administration (FDA) regulations for antibiotic API intermediates
    • ICH Q3A(R2) guideline for residual solvents and impurities

    Typical usage ratio

    • Generally 0.9–1.1 molar equivalents relative to the parent core; adjusted based on reactivity and desired substitution pattern

    Downstream process integration

    • Charged as the key brominated heterocyclic reactant during the intermediate synthesis stage prior to core peptide-side chain coupling; strict batch-wise verification and analytical release required

    Final product types

    • Semi-synthetic cephalosporin API intermediates
    • Third-generation cephalosporin active pharmaceutical ingredients
    • Custom novel antibiotics for clinical development

    2. Dye and Pigment Intermediate for Specialty Textile Formulations

    This compound is incorporated as a precursor in the synthesis of sulfur-containing heterocyclic dyes. Renowned textile chemical manufacturers utilize the chemical to introduce distinct substituent effects into chromophore backbones, delivering improved wash fastness and hue stability. Its performance under oxidative coupling conditions proves dependable for processes requiring high-purity intermediates and color uniformity, often feeding into continuous dye synthesis reactors producing high-volume textile colorants.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for restricted substances in textiles
    • ZDHC MRSL v3.1 (Zero Discharge of Hazardous Chemicals)
    • ISO 9001:2015 for pigment process controls
    • REACH Annex XVII substance restrictions

    Typical usage ratio

    • Typically 3–7% weight of finished dye, adjusted for target color depth and final chromophore substitution requirements

    Downstream process integration

    • Introduced during the initial synthesis of the dye intermediate, commonly dissolved with other aromatic reactants prior to oxidative coupling and post-processing purification

    Final product types

    • Reactive dyes for cotton and cellulosic fibers
    • Disperse dyes for polyester blends
    • Sulfur-based pigment blends for technical textiles

    3. Photographic Chemical Synthesis for Imaging Materials

    Manufacturers of high-resolution imaging materials incorporate 6-Bromo-2-Benzothiazolinone as a key intermediate for synthesizing light-sensitive heterocycle color developers. Stringent process control is vital, as these photochemical compounds demand sub-ppm purity and precise substitution to meet performance and compatibility standards for both medical imaging and industrial X-ray films. Our material integrates seamlessly into standard developer synthesis, contributing to enhanced sensitivity and gradation control in final photoproducts.

    Industry compliance standards

    • ISO 18902:2013 for imaging materials — processed films and safety requirements
    • GMP-like systems for photochemical manufacturing (site audits standard in the sector)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • REACH registration for manufacturing and end uses

    Typical usage ratio

    • Ranges from 0.5–2.5% by mass in the color developer formulation; adjusted depending on required image tone and resolution

    Downstream process integration

    • Dosed during the color developer complex formation, pre-mixing with phenolic or aminated aromatic partners under controlled temperature and inert atmosphere

    Final product types

    • Medical X-ray film color developers
    • Analog photographic paper and film chemicals
    • Industrial non-destructive testing imaging developers

    4. Agricultural Chemical Synthesis: Pesticide Intermediate for Fungicide Formulations

    Producers of modern agricultural fungicides utilize our material as a reactant in constructing benzothiazole-based ring structures, imparting targeted antifungal profiles to protect high-value crops. The compound’s controlled halogen placement is essential for selective biological activity, and our supply to the agrochemical market accompanies full traceability for regulatory registration. Typically, batch-wise QC supports integration into multistep manufacturing of technical-grade fungicidal actives that downstream formulators dilute or granulate for market-ready products.

    Industry compliance standards

    • FAO/WHO specification for pesticide technical materials
    • ISO 9001:2015 for full-scale agrochemical production
    • EU Regulation (EC) No 1107/2009 on plant protection product authorizations
    • EPA (US) registration dossiers for active ingredient intermediates

    Typical usage ratio

    • Generally 1.0–1.2 mol equivalents per target active structure; can be fine-tuned based on the desired substitution index and the crop or region of target application

    Downstream process integration

    • Incorporated at the key cyclization or halogenation stage during multi-step batch synthesis for technical-grade actives, with dedicated reactor cleaning to avoid cross-contamination of actives

    Final product types

    • Technical-grade heterocyclic fungicides
    • Wettable powder and liquid suspension agrochemical concentrates
    • Seed treatment and foliar application formulations
    Free Quote

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