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5-Bromo-2-Phenylbenzimidazole

    • Product Name 5-Bromo-2-Phenylbenzimidazole
    • Alias Hoechst 33258
    • Einecs 629-292-7
    • 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
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    Specifications

    HS Code

    444757

    Chemical Name 5-Bromo-2-Phenylbenzimidazole
    Cas Number 3982-63-4
    Molecular Formula C13H9BrN2
    Molecular Weight 273.13 g/mol
    Appearance Off-white to light yellow powder
    Melting Point 218-222 °C
    Purity Typically ≥98%
    Solubility Slightly soluble in DMSO, DMF, and chloroform
    Storage Conditions Store at room temperature, protect from light
    Synonyms 5-Bromo-2-phenyl-1H-benzimidazole
    Smiles Brc1ccc2nc(-c3ccccc3)nc2c1
    Inchi InChI=1S/C13H9BrN2/c14-10-6-7-12-13(8-10)16-11(15-12)9-4-2-1-3-5-9

    As an accredited 5-Bromo-2-Phenylbenzimidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White powder packaged in a sealed, amber glass bottle, 25 grams, labeled with chemical name, CAS number, and hazard warnings.
    Shipping 5-Bromo-2-Phenylbenzimidazole is shipped in sealed, chemical-resistant containers to prevent moisture or contamination. The package is clearly labeled with hazard symbols and handled as per standard chemical safety protocols. Transport complies with local, state, and international regulations for hazardous materials to ensure safe and secure delivery. Handle with care.
    Storage 5-Bromo-2-Phenylbenzimidazole should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Store it in a cool, dry, well-ventilated area away from sources of ignition and strong oxidizing agents. Proper labeling and secondary containment are advised. Always follow institutional and regulatory safety guidelines when handling and storing this chemical.
    Application of 5-Bromo-2-Phenylbenzimidazole

    Applications of 5-Bromo-2-Phenylbenzimidazole in Industrial Manufacturing

    As a specialized manufacturer, we supply 5-Bromo-2-Phenylbenzimidazole into key industrial sectors where its unique chemical characteristics fulfill specific product design and performance requirements. Below you will find a comprehensive overview of practical application scenarios, focusing on real downstream usage, integration points in production flows, and established industry compliance frameworks.

    1. Synthesis of Pharmaceutical Intermediates for Antiviral Compounds

    Pharmaceutical active ingredient manufacturers utilize 5-Bromo-2-Phenylbenzimidazole as a precursor for synthesizing heterocyclic scaffolds in antivirals targeting RNA polymerase inhibition. It enters proprietary multi-step synthesis processes, contributing structural motifs which enhance bioactivity in subsequent API molecules. Quality assurance, traceability, and residual bromine testing are managed in compliance with industry pharmacopeial requirements.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP (United States Pharmacopeia) monographs for intermediate and final product quality
    • European Pharmacopoeia (Ph. Eur.) standards
    • REACH Registration (for Europe-bound shipments)

    Typical usage ratio

    • Usually 0.5–2.5 molar equivalents per synthesis batch, adjusted per target product yield and outflows; ratio determined by desired reaction throughput and substrate reactivity in intermediate formation.

    Downstream process integration

    • Introduced at the heterocycle construction step, followed by coupling reactions, halogen exchange, or subsequent substitution; integrated into automated reactor trains within cGMP-compliant facilities.

    Final product types

    • Antiviral API intermediates (e.g., benzimidazole derivatives for COVID-19 and hepatitis therapies)
    • Final small-molecule drug substances prepared by related downstream synthesis

    2. High-Temperature Polymers and Advanced Material Performance Additives

    Industries producing high-performance engineering plastics and specialty resins adopt 5-Bromo-2-Phenylbenzimidazole as a building block to impart enhanced thermal stability and fire resistance. Its use focuses on chain extension and modification chemistry, particularly for aerospace, electronics encapsulation, and consumer electrical insulation components. Meticulous adherence to relevant thermal and emissions standards guides material qualification stages.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics Materials
    • RoHS Directive (2011/65/EU) for restricted substances
    • ISO 1043-1 for polymer identification and nomenclature
    • ASTM D2863 (Limiting Oxygen Index for flame retardancy assessment)

    Typical usage ratio

    • Blended at 0.8–2.1% by polymer weight, depending on targeted heat deflection temperature and flammability class; dose calculated in pilot formulation trials according to compounding parameters.

    Downstream process integration

    • Dispensed in the pre-polymerization or compounding stage, either via direct chemical copolymerization or as a reactive flame-retardant additive during melt processing; compatibility is confirmed with extrusion or injection molding systems.

    Final product types

    • FR (flame-retardant) polyimide and polyamide resins for electrical enclosures
    • Composite components for electronic connectors and relay bases
    • Heat-resistant automotive sensor housings

    3. Organic Light-Emitting Diode (OLED) and Electronic Material Synthesis

    Electronic material producers employ 5-Bromo-2-Phenylbenzimidazole for manufacture of custom organic intermediates in OLED emitter and charge transport layer materials. Its bromo-functionalized aromatic structure serves as a cross-coupling substrate in palladium-catalyzed C–N or C–C bond-forming reactions, essential for optoelectronic property tuning. Manufacturers implement strict documentation and traceability procedures to meet electronics sector purity requirements.

    Industry compliance standards

    • IEC 61249-2-21 standards for materials introduced into printed circuit boards
    • JEDEC JESD 625B Material Handling Standard
    • RoHS and REACH compliance for global electronics applications
    • 92/31/EEC (European directive on electromagnetic compatibility, relevant for display materials)

    Typical usage ratio

    • Reacted at 0.68–1.15 molar equivalents based on the stoichiometry of the cross-coupling reaction step; actual proportion depends on the molecular design of the target OLED intermediate.

    Downstream process integration

    • Loaded into anhydrous organic reaction systems under inert atmosphere, typically as an aryl bromide reactant in Suzuki, Buchwald-Hartwig, or Stille coupling protocols; followed by crystallization and high-vacuum purification.

    Final product types

    • Hole transport or electron transport materials for OLED displays
    • Customized benzimidazole derivatives for organic thin film transistors (OTFTs)
    • Functional intermediates for optoelectronic device fabrication

    4. UV Absorber and Stabilizer Synthesis in Industrial Coatings

    Formulators in the coatings industry use 5-Bromo-2-Phenylbenzimidazole to create UV-absorbing chemical scaffolds for protective clear coats and specialty paints. Its molecular core supports the design of high-efficiency stabilizers, which are subsequently reacted, functionalized, and incorporated to reduce polymer discoloration and extend service life of coated surfaces. Each production lot aligns with testing protocols established by regulatory and customer-specific requirements.

    Industry compliance standards

    • ISO 11507 (Artificial weathering exposure methods)
    • EN 71-3 (Safety of toys – migration of certain elements, relevant for toy coatings)
    • ASTM D4587 (UV exposure testing) and ASTM G154 (UV/condensation apparatus standards)
    • REACH Annex XVII (restrictions due to toxicological profile in finished goods)

    Typical usage ratio

    • Converted in-house to target stabilizer at a calculated conversion of 1.1–1.3 molar equivalents per reaction, afterward dosed at 0.15–0.35% by total coating resin weight to optimize UV resistance without jeopardizing end-use regulatory limits.

    Downstream process integration

    • First processed through synthesis of benzimidazole-based UV stabilizer, then let down into industrial resin matrix during the pigment dispersion or clear coat top-off stage; QC follows simulated aging and UV resistance criteria.

    Final product types

    • UV-protection clear and pigmented coatings for automotive exteriors
    • Weather-resistant industrial finishes for plastic and metal substrates
    • Protective exterior wood coating formulations
    Free Quote

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