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1,2-Bis(Diphenylphosphino)Benzene

    • Product Name 1,2-Bis(Diphenylphosphino)Benzene
    • Alias DPPB
    • Einecs 227-823-9
    • 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
    VTB
    Specifications

    HS Code

    159910

    Cas Number 1663-45-2
    Iupac Name 1,2-Bis(diphenylphosphanyl)benzene
    Molecular Formula C30H24P2
    Molar Mass 446.45 g/mol
    Appearance White to off-white solid
    Melting Point 210-213 °C
    Solubility Soluble in organic solvents (e.g., dichloromethane, toluene)
    Purity Typically ≥98%
    Smiles c1ccc(cc1)P(c2ccccc2)c3ccccc3P(c4ccccc4)c5ccccc5
    Synonyms DPPB; o-Phenylenebis(diphenylphosphine)
    Density 1.24 g/cm³ (approximate)
    Boiling Point Decomposes before boiling
    Storage Conditions Store under inert atmosphere, protect from moisture and air
    Hazard Statements May cause skin and eye irritation

    As an accredited 1,2-Bis(Diphenylphosphino)Benzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g quantity of 1,2-Bis(Diphenylphosphino)Benzene is packaged in a sealed amber glass bottle with tamper-evident cap.
    Shipping 1,2-Bis(Diphenylphosphino)Benzene is shipped in tightly sealed containers to prevent moisture and air exposure. It should be packed in inert atmosphere packaging, cushioned to avoid breakage. Store and transport at room temperature, complying with all local, national, and international regulations regarding the shipment of chemical substances. Handle with care.
    Storage 1,2-Bis(diphenylphosphino)benzene should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Keep it in a cool, dry place away from moisture and direct sunlight. Store it separately from oxidizing materials and sources of ignition. Use appropriate personal protective equipment when handling this chemical.
    Application of 1,2-Bis(Diphenylphosphino)Benzene

    Applications of 1,2-Bis(Diphenylphosphino)Benzene in Industrial Manufacturing

    As the direct manufacturer of 1,2-Bis(Diphenylphosphino)Benzene (DPPB), we service multiple specialized chemical sectors. Our DPPB supports advanced catalyst systems and highly specific transformations across organometallic, pharmaceutical, polymer, electronic, and fine chemical industries. Below, we outline the principal industrial application scenarios, technical integration points, and compliance pathways specific to each downstream segment.

    1. Homogeneous Catalysis for Fine Chemical Synthesis

    DPPB functions as an efficient ligand in the formulation of metal-complex catalysts, especially in processes such as asymmetric hydrogenation, hydroformylation, and cross-coupling reactions within fine chemical manufacturing plants. End users select DPPB for its defined bite angle and electronic properties, enabling increased selectivity and turnover in both pilot and commercial scale processes. Catalysts based on DPPB support the synthesis of advanced intermediates for flavors, agrochemical actives, and specialty compounds. Exact formulation ratios depend on the metal center and target transformation, with application dictated by production scale and downstream product purity specifications.

    Industry compliance standards

    • REACH Registration for use in industrial synthesis (EC No. 216-086-1)
    • Responsible Care® Initiative (International Council of Chemical Associations)
    • ISO 9001:2015 Quality Management System for chemical processing
    • GMP guidelines for fine chemical intermediates where applicable

    Typical usage ratio

    • 0.5–3 mol% relative to metal content, adjusted for substrate reactivity and desired catalytic performance. Process engineers verify active loading during batch optimization cycles.

    Downstream process integration

    • DPPB enters during catalyst assembly in the reactor charge step. Operators combine DPPB with transition metal precursors under inert atmosphere, forming the active complex in situ prior to substrate addition. QC monitors ligand purity during catalyst pre-activation.

    Final product types

    • Chiral amines and alcohols
    • Specialty aldehydes
    • Pharmaceutical building blocks
    • Pheromones and specialty aroma compounds

    2. Ligand in Pharmaceutical Active Ingredient Synthesis

    Within cGMP-regulated pharmaceutical manufacturing, DPPB serves as a ligand in metal-catalyzed transformations, especially during key C-C and C-N bond-forming steps in active pharmaceutical ingredient (API) production. Its rigid bidentate coordination supports consistent stereochemical outcomes and minimizes batch-to-batch variation. End users apply DPPB for palladium-catalyzed Suzuki, Sonogashira, and Buchwald-Hartwig couplings, which form critical intermediates or late-stage API derivatives. The integrity of DPPB and its documented traceability meet audit requirements for regulated pharmaceutical manufacturing environments.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP-NF and EP compendia (for trace metal and ligand residuals in APIs)
    • FDA 21 CFR Part 211 (for quality systems in finished pharmaceuticals)
    • Specific drug master file (DMF) submissions in the United States, EU CEP filings where required

    Typical usage ratio

    • 0.1–2 mol% with respect to catalyst metal, customized based on step yield, impurity control, and downstream regulatory acceptance criteria.

    Downstream process integration

    • Used in reactor systems equipped for oxygen-sensitive chemistry, DPPB is dissolved in anhydrous solvents prior to metal salt addition. Pharmaceutical QC assays verify residual ligand post-process. Operators employ phase extraction or crystallization for ligand removal before API isolation.

    Final product types

    • Active pharmaceutical ingredients (small molecule drugs)
    • Complex drug intermediates
    • Advanced pharmaceutical intermediates (APIs-in-progress)
    • Precursor compounds for oncology and CNS drugs

    3. Catalytic Applications in Specialty Polymer Synthesis

    Many polymer modification and specialty polymerization processes utilize DPPB-based complexes to modulate polymer architecture, control molecular weight distributions, or facilitate living/controlled polymerizations. Our material supports precise phosphine ligand architecture in olefin polymerization and post-polymerization functionalization—especially where narrow PDI or targeted end-group functionality is required. Producers favor DPPB in the development of high-value engineering plastics and advanced elastomers with improved mechanical and chemical resistance profiles.

    Industry compliance standards

    • ISO 9001:2015 for specialty polymers
    • ASTM D883 (Standard Terminology Relating to Plastics)
    • EU Regulation (EC) No 1907/2006 (REACH) for polymer processing
    • Customer-specific specifications for allowable catalyst residues

    Typical usage ratio

    • 0.1–1.2 wt% as a ligand in catalyst formulation, with dosage determined by monomer type, target polymer structure, and metal center compatibility.

    Downstream process integration

    • Operators charge DPPB into the polymerization reactor during catalyst pre-treatment. After polymerization, downstream separation or purification steps remove residual ligand and metal per customer purity request.

    Final product types

    • Thermoplastic elastomer base resins
    • High-performance polyolefins
    • Specialty copolymers for automotive and electronics
    • Block copolymers for adhesives and sealants

    4. Synthesis of Organometallic Electronic Materials

    Manufacturers of advanced electronic materials use DPPB as a ligand in the synthesis of phosphine-coordinated transition metal complexes, especially for OLED precursors, organic semiconductors, and coordination compounds required for light-emitting or charge-transport functions. The defined electronic characteristics of DPPB give precise control over HOMO-LUMO gaps and tuning of photophysical properties in the final device infrastructure. Purity, reproducibility of spectral characteristics, and trace metal content must match electronics-grade specifications at every stage.

    Industry compliance standards

    • JEITA EM-360 (Material Guidelines for Organic Electronic Devices, Japan)
    • IEC 62899-201 (Printed electronics – Materials)
    • ISO 14644 (Cleanroom particle count for electronics manufacturing)
    • RoHS Directive 2011/65/EU (for residual metal and phosphorus content in device components)

    Typical usage ratio

    • 0.05–1 eq relative to metal center, determined by the coordination requirements of the target complex and batch size in pre-formulation labs.

    Downstream process integration

    • DPPB is solubilized and added during ligand exchange or direct complexation steps, followed by chromatographic purification to electronics-grade residual levels. Material is handled in controlled environment suites to minimize contamination for device critical parts.

    Final product types

    • OLED small molecule precursors
    • Phosphorescent emitters
    • Organic electronic semiconductors
    • Photoactive organometallic dyes
    Free Quote

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