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1-(4-Bromophenyl)Imidazole

    • Product Name 1-(4-Bromophenyl)Imidazole
    • Alias 4-Bromo-1-phenylimidazole
    • Einecs 629-506-2
    • 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

    378176

    Product Name 1-(4-Bromophenyl)Imidazole
    Molecular Formula C9H7BrN2
    Molecular Weight 223.07 g/mol
    Cas Number 17369-59-4
    Appearance White to off-white solid
    Melting Point 99-101°C
    Purity Typically >97%
    Solubility Soluble in DMSO, methanol
    Smiles Brc1ccc(cc1)n2ccnc2
    Inchi InChI=1S/C9H7BrN2/c10-8-3-1-7(2-4-8)12-6-5-11-9-12/h1-6H,9H2
    Storage Conditions Store at room temperature, in a dry and cool place

    As an accredited 1-(4-Bromophenyl)Imidazole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g bottle of 1-(4-Bromophenyl)imidazole is sealed in an amber glass container with a screw cap and safety label.
    Shipping 1-(4-Bromophenyl)Imidazole is shipped in tightly sealed containers, protected from light and moisture. It is handled in accordance with standard chemical shipping regulations, ensuring safe transit. Packages are clearly labeled and may require documentation for hazardous materials, depending on quantity and destination. Temperature control is maintained if necessary to preserve product integrity.
    Storage 1-(4-Bromophenyl)imidazole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as oxidizing agents. Protect from moisture and direct sunlight. Ensure proper labeling and limit exposure by using in a chemical fume hood. Store according to institutional and safety guidelines.
    Application of 1-(4-Bromophenyl)Imidazole

    Applications of 1-(4-Bromophenyl)Imidazole in Industrial Manufacturing

    1-(4-Bromophenyl)Imidazole serves as a key intermediate across several industrial sectors, particularly in pharmaceutical synthesis, specialty agrochemical production, advanced material development, and dye manufacturing. Its brominated aromatic structure and imidazole moiety enable precise downstream chemical transformations, supporting strict process control and high product yields.

    1. Pharmaceutical API Intermediate Synthesis

    Manufacturers use this compound in the synthesis of azole-based antifungal agents and investigational drug candidates. Its imidazole ring facilitates the construction of heterocyclic scaffolds, while the bromine atom enables targeted substitution or coupling reactions. Chemists introduce this intermediate during multi-stage sequence synthesis, including Suzuki and Buchwald-type cross-coupling, to generate pharmacologically active cores before final salt formation and purification.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) – ICH Q7 guidelines
    • EU EudraLex Volume 4 GMP
    • United States Pharmacopeia (USP) for process validation (where applicable for intermediates)
    • International Organization for Standardization ISO 9001:2015 for chemical intermediates

    Typical usage ratio

    • Applied in 0.8–1.2 molar equivalents relative to target API scaffold, depending on route optimization and yield targets
    • Adjusted based on reaction efficiency and subsequent purification requirements

    Downstream process integration

    • Introduced in the mid-stages of synthetic routes as the building block for azole rings
    • Undergoes halogenation, N-alkylation, or palladium-catalyzed coupling steps
    • Processed further with base or acid hydrolysis before entering final crystallization

    Final product types

    • Active pharmaceutical ingredients such as antifungal imidazoles
    • Investigational agents for CNS or oncology indications
    • Intermediate compounds for custom drug discovery projects

    2. Agrochemical Synthesis – Fungicide Precursors

    This raw material supports the industrial production of systemically active agrichemicals—especially triazole and imidazole fungicides. Application specialists dose this intermediate during field-use fungicide precursor assembly to impart broad-spectrum fungal protection. Bromine activation increases reactivity in nucleophilic aromatic substitution, enhancing the downstream introduction of protective groups or co-formulant moieties.

    Industry compliance standards

    • ISO 9001:2015 QMS for agrochemical synthesis
    • Food and Agriculture Organization (FAO) specification for pesticide active ingredients
    • REACH Regulation (EC) No 1907/2006 for chemical registration in Europe
    • OECD Principles of Good Laboratory Practice (GLP) for process development

    Typical usage ratio

    • Dosed at 1.0–1.5 molar ratio to target fungicide active group
    • Ratio fine-tuned according to downstream alkylation or acylation efficiency

    Downstream process integration

    • Added to batch reactors during the nucleophilic substitution phase
    • Couples with various co-reactants to yield azole-fungicide backbones
    • Subjected to high-shear mixing and temperature-controlled stages before final formulation

    Final product types

    • Systemic triazole and imidazole fungicides for crop protection
    • Intermediates for protective seed-treatment chemicals
    • Precursors for soil fungicide blends

    3. OLED and Electronic Material Development

    Producers use this compound for synthesizing functional imidazole derivatives deployed in organic light-emitting diode (OLED) emissive layers and electronic materials. The molecule’s aromatic-brominated motif facilitates site-selective substitution, supporting precision manufacturing of electron-transporting and hole-blocking materials. Material scientists insert this intermediate mainly in early-stage organic synthesis to construct performance-critical specialty polymers.

    Industry compliance standards

    • IPC-1752 Material Declaration Management Standard for electronics
    • RoHS Directive (2011/65/EU) for restricted substances in electronics
    • ISO 14001:2015 for environmental management in material manufacturing
    • REACH Regulation for handling and downstream user registration

    Typical usage ratio

    • Introduced at 0.6–1.1 molar equivalents relative to target polymer building units
    • Ratio depends on the specific electronic structure and desired luminescence or conductivity

    Downstream process integration

    • Supplied to organic synthesis reactors for functional group introduction
    • Undergoes subsequent cross-coupling or metallation steps for advanced OLED layers
    • Processed further in solution or melt-phase synthesis before film casting

    Final product types

    • OLED emissive and charge-transport layer compounds
    • Organic electronic substrates
    • Functionalized polymers for display panel manufacturing

    4. Specialty Dye and Pigment Intermediates

    1-(4-Bromophenyl)Imidazole acts as a precursor in the manufacture of high-performance dyes, particularly for use in printing inks and specialty polyester coloration. Its dual reactivity profile allows coloring chemists to install chromophoric substituents via controlled aromatic substitution. The bromine facilitates the attachment of donor-acceptor groups to deepen shade saturation or enhance photostability during final dye manufacture.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for dye production
    • EN 71-3:2019 (Migration of chemicals) for colorants in consumer goods
    • Oeko-Tex Standard 100 for textile dyes
    • REACH Authorization and Restriction of Chemicals for pigments and dyes

    Typical usage ratio

    • Utilized in 0.9–1.5 molar equivalents per target dye intermediate
    • Proportional adjustment based on chromophore complexity and target shade profile

    Downstream process integration

    • Reacted during the dye precursor formation stage in batch or continuous processing
    • Undergoes subsequent functionalization (amination, sulfonation, etc.) to fine-tune end-color properties
    • Integrated before final purification and formulation into commercial inks or pigment pastes

    Final product types

    • Disperse dyes for polyester
    • Reactive dye intermediates for paper and textile printing
    • High-stability pigments for specialty inks
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