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1-Bromo-2,6-Dichlorobenzene

    • Product Name 1-Bromo-2,6-Dichlorobenzene
    • Alias 1,2,6-Trichlorobromobenzene
    • Einecs 221-021-2
    • 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

    948231

    Name 1-Bromo-2,6-Dichlorobenzene
    Molecularformula C6H3BrCl2
    Molecularweight 240.90 g/mol
    Casnumber 827-52-1
    Appearance White to off-white solid
    Meltingpoint 42-44 °C
    Boilingpoint 248-250 °C
    Density 1.81 g/cm³
    Solubilityinwater Insoluble
    Flashpoint 115 °C
    Odor Aromatic
    Refractiveindex 1.589 (20 °C)
    Pubchemcid 123419

    As an accredited 1-Bromo-2,6-Dichlorobenzene 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 100 grams of 1-Bromo-2,6-Dichlorobenzene, tightly sealed with a screw cap and hazard labeling.
    Shipping 1-Bromo-2,6-dichlorobenzene is classified as a hazardous material for shipping. It should be packed in tightly sealed, compatible containers and clearly labeled according to relevant regulations (e.g., DOT, IATA). Ship in compliance with all chemical transport guidelines, ensuring appropriate documentation and precautions to prevent leakage, exposure, and environmental contamination.
    Storage Store 1-Bromo-2,6-dichlorobenzene in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight, heat, and sources of ignition. Keep it separate from incompatible materials such as strong oxidizers. Ensure proper labeling, and avoid storage near food or drinking water. Use appropriate chemical storage cabinets if available, and follow local regulations for hazardous chemicals.
    Application of 1-Bromo-2,6-Dichlorobenzene

    Applications of 1-Bromo-2,6-Dichlorobenzene in Industrial Manufacturing

    As an established producer of 1-Bromo-2,6-Dichlorobenzene, we supply this key halogenated aromatic intermediate to specialized manufacturers across the chemical sector. The following application segments detail targeted industrial uses backed by recognized compliance standards, industry-specific formulation ratios, exact points of process integration, and corresponding end-use products.

    1. Agrochemical Intermediate Manufacturing

    Agrochemical formulators employ 1-Bromo-2,6-Dichlorobenzene as a core intermediate in synthesizing specific fungicidal and herbicidal actives that rely on precise halogen patterns for selectivity and stability. The raw material enters the chlorination/bromination steps for building complex molecular frameworks, impacting the efficacy and environmental profile of final crop protection compounds.

    Industry compliance standards

    • FAO/WHO Specification for Pesticide Technical Grade
    • REACH Annex XVII for Agrochemicals (EU)
    • EPA FIFRA Regulations (USA)
    • China GB 2763 Maximum Residue Standard

    Typical usage ratio

    • Intermediate batch concentrations range from 12-18% w/w, adjusted for target halogen substitution yields and impurity control in the active ingredient formation stage.

    Downstream process integration

    • Material is introduced during the aromatic halogenation step of active ingredient synthesis prior to further condensation or coupling reactions.

    Final product types

    • Pre-formulated fungicide technical concentrates
    • Herbicide technical grade materials for emulsifiable concentrates
    • Pesticide active intermediates packaged for contract formulation

    2. Pharmaceutical Intermediate Synthesis

    Chemical process development teams in the pharmaceutical industry utilize this compound in multi-step syntheses of advanced pharmaceutical intermediates where its ortho-bromo, di-chloro structure is essential for constructing heterocyclic scaffolds and facilitating regioselective C–C or C–N coupling during drug precursor manufacturing. The batch-wise introduction ensures reliable synthesis results and consistent impurity profiles.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF for relevant APIs and intermediates
    • EU EudraGMP Volume 4, Part II
    • Chinese Pharmacopoeia standards for pharmaceutical intermediates

    Typical usage ratio

    • Mol ratios of 0.9–1.2 equivalents relative to target core structure, tuned to limit halide byproduct formation and optimize reaction yield in pilot and commercial scale runs.

    Downstream process integration

    • Fed at the halogen exchange or Suzuki/Miyaura cross-coupling stage within API intermediate construction, followed by isolation and further conversion to higher-value drug intermediates.

    Final product types

    • Chlorobrominated heterocyclic pharmaceutical intermediates
    • Specialty building blocks for patented drug APIs
    • Advanced intermediates for timeline compression in kilo-lab production

    3. Dye and Pigment Intermediate Production

    Manufacturers in the colorant industry rely on 1-Bromo-2,6-Dichlorobenzene to introduce bromo and chloro substituents into aromatic systems for creating color-stable dye and pigment intermediates. This ensures the resulting pigments feature required resistance to light, solvents, and chemicals in textile and plastics applications, while consistent impurity levels in the supply chain protect downstream process reproducibility.

    Industry compliance standards

    • EN 71-3 (EU) Safety Standard for Toy Colorants
    • ISO 787 (General Methods of Test for Pigments and Extenders)
    • REACH Annex XIV for Pigment Chemicals
    • OEKO-TEX® Eco-Passport standards for input chemicals

    Typical usage ratio

    • Standard addition ranges from 8–14% of dye intermediate mass, modulated based on chromophore yield targets and chromatographic purity in continuous and batch colorant synthesis.

    Downstream process integration

    • Substrate is loaded at the aromatic substitution or coupling process, furnishing pure-bromo/chloro substituted intermediates prior to further diazotization or condensation steps.

    Final product types

    • Quinoline-based pigment intermediates
    • Fast-acid and disperse dyes for textile printing
    • Heat-stable pigments for plastics masterbatch production

    4. Specialty Polymer Synthesis

    Producers of high-performance engineering polymers integrate this halogenated aromatics intermediate during the polymer backbone functionalization step. Its unique substitution pattern modifies reactivity and imparts improved thermal and chemical resistance properties in specialty resins and thermoplastics, important for electrical, electronic, and automotive parts manufacturing that must pass strict regulatory performance tests.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics
    • RoHS Directive (EU) for Electronic Components
    • ASTM D638 for Mechanical Properties of Plastics
    • ISO 1043-1 for Polymer Additive Nomenclature

    Typical usage ratio

    • Introduced at 3–10% by polymer recipe mass, subject to adjustments for molecular weight control and desired halogen content in reaction monitoring.

    Downstream process integration

    • Feeds directly into the monomer functionalization stage or co-polymerization reactor for specialty polymer chain assembly, monitored by QC to ensure reproducible additive levels.

    Final product types

    • Halogenated engineering thermoplastics for automotive connectors
    • Flame-retardant resins for PCB and electronics housing
    • Custom molding compounds for high-specification industrial parts

    5. Fine Chemical Building Block Manufacture

    Producers of complex fine chemicals utilize this compound as a high-purity halide source for constructing advanced molecules used in chemical research, new material development, and specialized laboratory reagents. The material’s defined halogen profile enables precision-oriented synthesis, where trace impurities or substitutions can drastically impact research or formulation outcomes.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System for Chemical Production
    • OECD Guidelines for Testing of Chemicals
    • REACH Annex I for Laboratory Chemicals
    • GHS Classification and Labeling for Laboratory Use

    Typical usage ratio

    • Reagent-grade processes utilize 15–25 mmol per reaction, tailored by application scope, target molecule complexity, and analytical purity requirements.

    Downstream process integration

    • Charged during halide insertion, electrophilic aromatic substitution, or cross-coupling stages in multistep fine chemical synthesis, with batch purity confirmed by HPLC or GC methods.

    Final product types

    • Aryl bromide laboratory reagents
    • Multi-functional chemical building blocks for R&D pipelines
    • Custom fine chemicals for academic and pilot-scale research
    Free Quote

    Competitive 1-Bromo-2,6-Dichlorobenzene prices that fit your budget—flexible terms and customized quotes for every order.

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