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2-(Diphenylphosphino)Benzoic Acid

    • Product Name 2-(Diphenylphosphino)Benzoic Acid
    • Alias DPPBA
    • Einecs 222-161-1
    • 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

    477050

    Productname 2-(Diphenylphosphino)Benzoic Acid
    Casnumber 2626-37-7
    Molecularformula C19H15O2P
    Molecularweight 306.29
    Appearance White to off-white powder
    Meltingpoint 207-211 °C
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents
    Boilingpoint Decomposes before boiling
    Storagecondition Store at 2-8°C, under inert atmosphere
    Density 1.27 g/cm³
    Synonyms o-(Diphenylphosphino)benzoic acid

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

    Packing & Storage
    Packing Amber glass bottle containing 5 grams of 2-(Diphenylphosphino)benzoic acid, sealed with a screw cap and labeled for laboratory use.
    Shipping 2-(Diphenylphosphino)benzoic acid is shipped in tightly sealed containers, protected from moisture and air. It should be transported at room temperature, away from incompatible substances and direct sunlight. Packaging complies with chemical safety regulations to prevent leaks or spills. Handle with appropriate personal protective equipment during receipt and unpacking.
    Storage 2-(Diphenylphosphino)benzoic acid should be stored in a cool, dry, and well-ventilated area, protected from light and moisture. Keep the container tightly closed when not in use. Store away from incompatible materials such as strong oxidizing agents and acids. Recommended storage is under inert atmosphere (e.g., nitrogen or argon) to prevent oxidation of the phosphine group.
    Application of 2-(Diphenylphosphino)Benzoic Acid

    Applications of 2-(Diphenylphosphino)Benzoic Acid in Industrial Manufacturing

    2-(Diphenylphosphino)Benzoic Acid serves as a critical specialty intermediate throughout various organometallic, pharmaceutical, and advanced materials industries. As a direct manufacturer, we supply this compound to clients with diverse high-purity and process integration requirements, supporting downstream innovation and regulatory compliance.

    1. Homogeneous Catalysts for Cross-Coupling Reactions

    This compound functions as a chelating ligand in the synthesis of palladium and nickel complexes used for Suzuki-Miyaura and Buchwald-Hartwig cross-coupling. Industrial catalyst suppliers incorporate it to tailor electronic and steric properties, improving selectivity in large-scale synthesis of fine chemicals and API intermediates. Reaction engineers set dosage according to metal-to-ligand ratios, impacting catalyst turnover and substrate conversion in batch and continuous flow reactors.

    Industry compliance standards

    • ISO 9001:2015 Quality Management System
    • REACH registration requirements (EU chemicals legislation)
    • ICH Q7 GMP Guidelines for Active Pharmaceutical Ingredient Manufacturing (if ligands enter pharma)
    • European Pharmacopeia General Monographs (for relevant pharmaceutical applications)

    Typical usage ratio

    • 0.8–1.2 molar equivalents per transition metal precursor for pre-catalyst synthesis
    • 0.1–2 wt% relative to substrate load in catalytic batch processes, depending on substrate complexity and catalyst recyclability

    Downstream process integration

    • Dissolve the acid in anhydrous solvent, combine with metal salt under inert atmosphere for ligand exchange; follow with in situ catalyst activation pre-charging into reactors
    • Used in continuous stirred-tank reactors (CSTRs) and fixed-bed catalytic modules for specialty chemicals manufacturing

    Final product types

    • Pharmaceutical intermediates produced via cross-coupling
    • Fine chemicals (biaryls, arylamines, and aryl ethers)
    • Agrochemical precursors and building blocks
    • Catalyst kits for large-scale synthetic plants

    2. Ligand Source in Organometallic Complex R&D

    Research groups and advanced materials developers use this material to synthesize novel phosphine-metal complexes for new functional materials, coordinated polymers, and OLED device fabrication. Precise control of the phosphine donor’s environment enables material scientists to design next-generation photosensitizers and electronic components. The compound’s carboxylic group supports anchoring on functionalized surfaces during device assembly.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for R&D labs in regulated sectors
    • ISO 17025:2017 for analytical testing labs
    • Material safety conformity to GHS (Globally Harmonized System)
    • RoHS Directive 2011/65/EU (for electronic applications in the EU)

    Typical usage ratio

    • 0.5–3 molar equivalents, adjusted per target complex geometry and coordination environment
    • 1–10 wt% loading onto device substrates or anchoring phases in material fabrication workflows

    Downstream process integration

    • Combine in situ with metal precursors at laboratory or pilot scale, followed by purification and structural characterization
    • Immobilize on solid-state surfaces pre- or post-coordination for device assembly sequences

    Final product types

    • OLED emitter components
    • Photosensitizer complexes for solar energy devices
    • Functional electrode materials
    • Chemical reagent kits for R&D and pilot-scale manufacturing

    3. Building Block in API (Active Pharmaceutical Ingredient) Intermediate Synthesis

    Synthetic pharmaceutical manufacturers employ this compound in building API intermediates through metal-catalyzed coupling and functionalization steps. The presence of both phosphine and carboxyl functional groups enables multi-step transformations under controlled GMP conditions. Chemists optimize the reagent ratio and handling to limit residual metals and meet regulatory impurity profiles.

    Industry compliance standards

    • EU GMP EudraLex Vol 4: Part II – Basic Requirements for Active Substances
    • US FDA 21 CFR Part 210/211 for Finished Pharmaceuticals
    • Japanese Pharmacopoeia general tests for related substances
    • USP <232>/<233> for elemental impurities (where applicable)

    Typical usage ratio

    • 0.5–1.5 molar equivalents per coupling or ligation step; adjusted to minimize excess and byproduct formation
    • Strictly controlled in multi-step API synthesis, with comprehensive mass-balance calculations

    Downstream process integration

    • Metered into reaction vessels during catalytic coupling or ligation stages under validated process conditions
    • Removed and quantified prior to final purification and crystallization steps

    Final product types

    • Small-molecule drug candidates
    • API intermediates with phosphine-derived scaffolds
    • Registered pharmaceutical substances manufactured for global markets
    • Pilot-scale cGMP samples for regulatory submission

    4. Phosphine Ligand for Specialty Polymerization Catalysts

    Polymer industry producers incorporate this acid as a ligand precursor in the development of coordination catalysts used in precise polymer structure control. The carboxylic function improves immobilization onto catalyst supports for high-activity Ziegler–Natta and metallocene-type catalyst systems. Technicians tune loading based on polymerization activity profiles during scale-up.

    Industry compliance standards

    • ISO 14001:2015 Environmental Management (polymer production facilities)
    • ASTM D3576 – Purity of Catalyst Components
    • REACH Safety Data Sheet (required for all EU supply chains)
    • Internal QMS benchmarking for specialty polymers

    Typical usage ratio

    • 0.05–0.5 molar equivalents based on metal species in catalyst precursor synthesis
    • Lower ratios (typically 0.01–0.05 wt%) for nanostructured polymerizations to avoid catalyst fouling

    Downstream process integration

    • Add to catalyst synthesis blend during initial ligand complexation step
    • Anchor ligand on silica or polymer-supported phases prior to reactor charging

    Final product types

    • High-performance engineering plastics
    • Specialty polyolefins and block copolymers
    • Polymer-grade catalyst masterbatches
    • Supported catalyst systems for process licensors
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