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(4-Bromobutyl)Triphenylphosphonium Bromide

    • Product Name (4-Bromobutyl)Triphenylphosphonium Bromide
    • Alias (4-Bromobutyl)triphenylphosphonium bromide
    • Einecs 629-360-9
    • 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

    420419

    Chemical Name (4-Bromobutyl)Triphenylphosphonium Bromide
    Cas Number 16809-26-6
    Molecular Formula C22H22Br2P
    Molecular Weight 475.20 g/mol
    Appearance White to off-white powder
    Melting Point 173-177°C
    Solubility Soluble in water and polar organic solvents
    Storage Conditions Store at room temperature, keep container tightly closed
    Purity Typically ≥98%
    Synonyms 4-Bromobutyltriphenylphosphonium bromide
    Smiles BrCCCC[P+](c1ccccc1)(c2ccccc2)c3ccccc3.[Br-]
    Inchi InChI=1S/C22H22BrP.BrH/c23-17-9-16-24(18-19-20-12-4-1-5-13-20,21-14-6-2-7-15-21,22-10-8-3-11-22)/h1-15H,16-19H2;1H/q+1;/p-1

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

    Packing & Storage
    Packing (4-Bromobutyl)triphenylphosphonium bromide is supplied in a 5g amber glass bottle with a screw cap, securely sealed and clearly labeled.
    Shipping (4-Bromobutyl)Triphenylphosphonium Bromide should be shipped in tightly sealed containers, protected from moisture and light. The chemical must be handled as a hazardous material and transported according to local, national, and international regulations. Proper labeling and documentation are required to ensure safety during transit. Temperature control is recommended if specified by the manufacturer.
    Storage **(4-Bromobutyl)triphenylphosphonium bromide** should be stored in a tightly sealed container, away from moisture and incompatible materials such as strong oxidizers. Keep it in a cool, dry, well-ventilated area, ideally at room temperature (15–25°C). Protect from light and direct heat sources. Ensure proper labeling and store in accordance with local chemical storage regulations.
    Application of (4-Bromobutyl)Triphenylphosphonium Bromide

    Applications of (4-Bromobutyl)Triphenylphosphonium Bromide in Industrial Manufacturing

    (4-Bromobutyl)Triphenylphosphonium Bromide serves advanced roles in several specialized chemical synthesis environments. As the original producer, we focus on consistently high-purity output, traceable quality, and batch-to-batch reliability, ensuring downstream manufacturers meet strict compliance and processing requirements. The following real-world application scenarios detail how manufacturers utilize this compound, with focus on formulation specifics and regulatory compliance.

    1. Pharmaceutical Intermediate Synthesis for Quaternary Ammonium Antibacterials

    Pharmaceutical manufacturers select this phosphonium salt for alkylation steps in the synthesis of quaternary ammonium compounds. Its bromoalkyl structure allows for precise introduction of butyl chains onto pharmacophores, supporting the creation of potent antibacterial agents. Handling at this stage requires close compliance with both synthesis safety protocols and active ingredient residual limits.

    Industry compliance standards

    • ISO 9001:2015 for QC traceability
    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • Ph. Eur. and USP monographs for related starting materials
    • REACH registration under EC Regulation 1907/2006

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to nucleophile, adjusted per active intermediate conversion rate, and verified by endpoint HPLC

    Downstream process integration

    • Introduced via controlled addition to the alkylation or quaternization reactor under inert atmosphere, after substrate charging and prior to base addition in stepwise temperature-controlled synthesis

    Final product types

    • Cationic pharmaceutical intermediates
    • Antimicrobial or antiseptic agents for topical formulations
    • Preservative actives for oral hygiene solutions
    • Bulk drug substances for finished dosage form production

    2. Phase-Transfer Catalyst Precursor Production

    Manufacturers of phase-transfer catalysts employ this compound to produce phosphonium-based systems. These are valued in industrial-scale biphasic synthesis, especially for nucleophilic substitution and oxidation reactions where transfer efficiency between organic and aqueous phases must meet yield and purity targets within defined operating conditions.

    Industry compliance standards

    • ISO 14001 for environmental management in catalyst production
    • Standard Operating Procedures (SOP) for hazardous chemical handling (Occupational Safety and Health Administration 29 CFR 1910.1200)
    • Chemical process safety under Process Safety Management (PSM) regulations
    • Internal corporate specifications for catalyst purity minimums (typically >99%)

    Typical usage ratio

    • Batch formulations use 1.0-1.3 equivalents, depending on nucleophile reactivity and target conversion rate; ratio determined by pilot yields and scalability assessments

    Downstream process integration

    • Charged directly to the reactor at initial blending, co-dissolved or suspended in appropriate solvent to ensure homogeneity before addition of secondary reactants

    Final product types

    • Trialkylphosphonium and tetraalkylphosphonium salts
    • Custom phase-transfer catalyst blends for pharma or agrochemical synthesis
    • Industrial catalysts for halide exchange and Williamson ether synthesis
    • Catalyst intermediates for further functional group modification

    3. Ion-Exchange Membrane Material Modification

    Specialty polymer manufacturers incorporate this phosphonium bromide into cross-linking or grafting protocols for ion-conductive membranes. The controlled quaternization enabled by this reagent enhances membrane selectivity and stability, supporting applications in energy devices and chemical separations where ionic conductivity and chemical resistance are paramount.

    Industry compliance standards

    • ISO 9001:2015 for documented process controls
    • IEC 62321 for safety assessment of materials in electrochemical environments
    • RoHS compliance for restricted hazardous substances
    • ISO 14040 for life-cycle assessment in advanced materials

    Typical usage ratio

    • Typically 5–15% by weight relative to the polymer backbone; adjusted based on target ion-exchange capacity, confirmed through post-grafting capacity tests

    Downstream process integration

    • Added to the polymer modification reactor during the quaternization or post-polymerization grafting phase, following pre-swelling and prior to membrane casting or extrusion

    Final product types

    • Alkaline ion-exchange membranes for fuel cell stacks
    • Anion-exchange membranes for electrodialysis systems
    • Polymeric separation membranes for industrial water treatment
    • Bipolar membranes for redox flow batteries

    4. Organic Synthesis Building Block for Advanced Materials Development

    Materials science laboratories and industrial synthesis plants utilize this reagent as a bromobutyl donor for the construction of functionalized organophosphorus compounds. These serve as key components in organic electronics, chromatography stationary phases, and specialty surfactants, where molecular structure precision affects downstream performance attributes.

    Industry compliance standards

    • ISO 17025 accreditation for analytical traceability in R&D
    • Responsible Care® program compliance (chemical management)
    • REACH (EC 1907/2006) registration for new materials
    • Company-specific new material evaluation protocols

    Typical usage ratio

    • Reagent charge typically 1.0–1.1 equivalents per nucleophile for precise stoichiometry; excess may be minimized to reduce purification load

    Downstream process integration

    • Dosed into the organic synthesis reaction vessel with cooling and inert protection, timed to ensure complete reaction and allow scalable downstream functionalization

    Final product types

    • Functionalized organophosphorus ligands for homogeneous catalysis
    • Customized stationary phases for high-performance liquid chromatography (HPLC)
    • Precursor molecules for cationic surfactants in specialty formulations
    • Component molecules for advanced functional polymers in electronic applications
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