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3-Bromo-1-Benzothiophene

    • Product Name 3-Bromo-1-Benzothiophene
    • Alias 3-Bromobenzo[b]thiophene
    • Einecs 211-872-0
    • 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

    828913

    Productname 3-Bromo-1-Benzothiophene
    Casnumber 585-76-2
    Molecularformula C8H5BrS
    Molecularweight 213.10
    Appearance Light yellow to brown solid
    Meltingpoint 37-41°C
    Boilingpoint 307°C
    Density 1.6 g/cm³
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles Brc1c2ccccc2s1
    Inchikey OBBTVTCKFDWBEQ-UHFFFAOYSA-N

    As an accredited 3-Bromo-1-Benzothiophene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle with tamper-evident cap, labeled “3-Bromo-1-Benzothiophene, 25g,” hazard and handling symbols clearly displayed.
    Shipping 3-Bromo-1-Benzothiophene is shipped in tightly sealed containers to prevent moisture and contamination. It is packed according to hazardous material regulations, typically under inert gas, and labeled appropriately. Shipping is conducted via certified carriers with necessary documentation and safety data, ensuring compliance with national and international transport regulations for chemicals.
    Storage Store **3-Bromo-1-Benzothiophene** in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and protected from light and moisture. Use appropriate chemical-resistant containers. Ensure proper labeling and access only to trained personnel, with suitable precautions for handling hazardous organic compounds.
    Application of 3-Bromo-1-Benzothiophene

    Applications of 3-Bromo-1-Benzothiophene in Industrial Manufacturing

    As a direct manufacturer, we supply 3-Bromo-1-Benzothiophene for downstream customers engaged in advanced materials synthesis, API intermediates, and specialty chemical production. Our application support ensures that formulation and process engineers can integrate this core intermediate into their flow with efficiency, batch reliability, and regulatory alignment. Below are key industry application scenarios—each detailing compliance, recipe information, factory-stage process, and end product forms—where this compound delivers specific functionality in commercial-scale manufacturing environments.

    1. Pharmaceutical Intermediate for Antifungal Agents

    Leading pharmaceutical companies employ this compound as a critical intermediate in the synthesis of antifungal drug candidates, particularly in benzothiophene-structured actives. The compound heads multi-stage synthesis chains for producing APIs such as selective estrogen receptor modulators, which require this heterocycle with precise halogen substitution. Its commercial supply centers on consistent purity tracked to pharmacopoeial quality and traceable batch records.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia, section 5.2.8 for pharmaceutical starting materials
    • US FDA DMF (Drug Master File) submission requirements
    • ISO 9001:2015 Quality Management System for documentation and traceability

    Typical usage ratio

    • Ranges from 0.8 to 1.3 mol/mol per target API, depending on route and stoichiometry adjustments during process scale-up, particularly in the step adding benzothiophene backbone

    Downstream process integration

    • Charged during early-stage synthesis post-protection/deprotection of thiophene ring; often follows halogen-metal exchange or Suzuki coupling, prior to chiral resolution or side chain modification

    Final product types

    • Benzothiophene-derived antifungal actives (e.g., experimental and generic agents)
    • SERMs (Selective Estrogen Receptor Modulators)
    • Research chemicals for preclinical medicine development

    2. Agrochemical Intermediate for Fungicide Synthesis

    This compound supports agrochemical manufacturers producing triazole or strobilurin fungicides where benzothiophene units contribute to potency and selectivity. Downstream customers introduce the intermediate at key coupling steps for patented and off-patent crop protection products with regulatory clearance for field use, subject to strict residue and synthesis controls under national crop chemical regulations.

    Industry compliance standards

    • FAO/WHO International Code of Conduct on Pesticide Management
    • GB 2763 Maximum Residue Limits (China) for active agrochemical ingredients
    • REACH Annex XVII for manufacturing and supply (EU)
    • ISO 17025 certified quality control of all raw materials and final actives

    Typical usage ratio

    • Applied at 1.0–1.3 molar equivalents per fungicide product batch; small scale process development may titrate this to match specific target impurity thresholds and yield objectives

    Downstream process integration

    • Fed into palladium-catalyzed coupling and heterocycle condensation reactors after upstream formation of thiophene core; inclusion monitored by in-process HPLC for stepwise synthesis validation

    Final product types

    • Benzothiophene-containing triazole fungicides
    • Strobilurin crop protection actives
    • Blended technical-grade agrochemical products

    3. Advanced Material Synthesis for Organic Semiconductors

    Electronics material producers depend on this specialty raw material as a core building block for constructing organic semiconductor layers used in organic thin-film transistors and OLED (organic light-emitting diode) device prototypes. Here, the compound’s bromo-substituted thiophene enhances electronic performance and stability in finished materials, and formulations must meet the microelectronic industry’s exacting contamination and purity controls.

    Industry compliance standards

    • IPC-1752 material declaration for electronic assemblies
    • RoHS Directive (2011/65/EU) compliance for heavy metal and organic content
    • SEMI C59-0998 purity specifications for organics in electronics manufacturing
    • REACH compliance for all monomer-level industrial applications

    Typical usage ratio

    • Commonly used at 15–30% w/w in the monomer mixture feeding polymerization reactors, with the proportion adjusted to tune polymer chain length and charge mobility properties

    Downstream process integration

    • Added as a co-monomer or precursor for Suzuki or Stille coupling polymerization; enters reactor feed as purified solid or solution, followed by film casting and annealing during device substrate fabrication

    Final product types

    • Small-molecule organic semiconductors
    • OLED emissive and transport materials
    • Soluble precursor inks for thin-film electronics patterning

    4. Intermediate for Specialty Dye Manufacture

    Producers of specialty dyes use this compound to introduce a distinctive bromo-benzothiophene motif into dye molecules, affecting absorption wavelength, stability, and fastness characteristics required for technical applications such as laser marking, industrial sensors, or security printing. The intermediate enters multi-step dye synthesis, typically within proprietary coupling or addition chemistry under regulated workplace exposure controls.

    Industry compliance standards

    • OEKO-TEX® Standard 100–class IV for colorant raw materials
    • EN 71-3 safety requirements for substances in industrial coatings and colorants
    • Clean Air Act MACT standards for dye and pigment production (US EPA)
    • REACH SVHC (Substances of Very High Concern) registration for dye intermediates

    Typical usage ratio

    • Between 5–12% by mass of target dye synthesis batch, optimized for chromophore content and exhaust/uptake during downstream blending or application

    Downstream process integration

    • Integrated post-azo or anthraquinone coupling, in sealed batch reactors under nitrogen protection, then subjected to filtration and purification ahead of dye isolation

    Final product types

    • Infrared-absorbing dyes for technical textiles and inks
    • Security pigments for anti-counterfeiting applications
    • Colorant intermediates for high-fastness specialty inks
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