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Bis(Tri-Tert-Butylphosphine)Palladium(0)

    • Product Name Bis(Tri-Tert-Butylphosphine)Palladium(0)
    • Alias Pd(PtBu3)2
    • Einecs 252-008-5
    • 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

    270366

    Chemical Name Bis(Tri-Tert-Butylphosphine)Palladium(0)
    Molecular Formula C24H54P2Pd
    Cas Number 14221-01-3
    Appearance Yellow to orange solid
    Melting Point 62-65°C
    Solubility Soluble in hydrocarbon and aromatic solvents; insoluble in water
    Storage Conditions Store under inert atmosphere, away from air and moisture
    Sensitivity Air and moisture sensitive
    Purity Typically ≥99%
    Density 1.19 g/cm³ (approximate)
    Smiles CC(C)(C)P(CC(C)(C)C)CC(C)(C)C.Pd
    Inchi InChI=1S/2C12H27P.Pd/c2*1-11(2,3)13(12(4,5)6)10-9-13;/h2*9-10H2,1-8H3;

    As an accredited Bis(Tri-Tert-Butylphosphine)Palladium(0) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 1-gram amber glass vial, tightly sealed under inert atmosphere, with a tamper-evident cap and hazard labeling.
    Shipping **Shipping Description**: Bis(Tri-Tert-Butylphosphine)Palladium(0) is typically shipped in sealed containers under inert atmosphere (argon or nitrogen) to prevent air and moisture exposure. It should be kept cool and dry during transport. Classified as a hazardous chemical, shipping must comply with relevant safety, labeling, and documentation regulations.
    Storage Bis(Tri-Tert-Butylphosphine)Palladium(0) should be stored in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent oxidation. Store it in a cool, dry place away from light, heat, and moisture. Avoid contact with air and water, as this compound is air-sensitive and decomposes upon exposure. Handle inside a glovebox or using Schlenk techniques.
    Application of Bis(Tri-Tert-Butylphosphine)Palladium(0)

    Applications of Bis(Tri-Tert-Butylphosphine)Palladium(0) in Industrial Manufacturing

    As the direct manufacturer, we supply Bis(Tri-Tert-Butylphosphine)Palladium(0) to large-scale partners who require highly selective and reliable catalysis in organic and organometallic syntheses. The following industrial sectors represent principal downstream application scenarios for this material, each with tailored compliance, formulation methods, unique downstream integration, and concrete final products.

    1. Pharmaceutical API C-C Coupling Synthesis

    Major pharmaceutical companies employ this catalyst in Buchwald–Hartwig and Suzuki-Miyaura couplings to synthesize complex active pharmaceutical ingredients containing aryl–aryl and aryl–amine bonds. Reaction consistency is essential where trace-level contamination and residual metals must remain within ICH Q3D limits. Developers precisely adjust catalyst charge based on substrate loading, impurity profile, and batch scale. The material integrates into multi-step GMP API synthesis after intermediate isolation, facilitating high-purity, scalable production of advanced intermediates and APIs.

    Industry compliance standards

    • ICH Q3D Guideline for Elemental Impurities
    • European Pharmacopoeia (Ph. Eur.) Monographs
    • US FDA cGMP 21 CFR Part 211
    • Chinese Pharmacopoeia

    Typical usage ratio

    • 0.01–1 mol% relative to substrate; optimized through process R&D based on palladium residual limits and yield balance

    Downstream process integration

    • Added at batch charging in the key coupling step after solvent and base addition
    • Removed post-reaction by aqueous extraction or filtration before next synthesis stage
    • Integrated process QC for palladium trace quantification

    Final product types

    • Active Pharmaceutical Ingredients (APIs) for oncology, antivirals, and central nervous system therapies
    • Pharmaceutical advanced intermediates with heteroaryl moieties

    2. Electronic Materials: OLED Intermediate Synthesis

    Producers of functional components for organic light-emitting diode (OLED) displays use our catalyst for constructing bifunctional aryl linkers in light-emitting materials. The material allows precise molecular architecture, necessary for device consistency and performance. Plants adopt electronic-industry cleanliness requirements over the full processing cycle to avoid contamination that affects emission efficiency. Chemists adjust catalyst input depending on ligand steric requirements and batch vessel scale. Downstream, the catalyst feeds into multi-step synthesis during critical cross-coupling or amination stages. Residues are managed using metal scavenging resins prior to purity-sensitive device integration.

    Industry compliance standards

    • IPC-5704 (Cleanliness Requirements for Unpopulated Printed Boards)
    • ISO 9001 Quality Management Systems (applicable to electronic material manufacturing)
    • Restrictive on trace heavy metals under RoHS/REACH

    Typical usage ratio

    • 0.05–0.8 mol% relative to aryl halide; determined by substrate reactivity, ligand load, and product purity target

    Downstream process integration

    • Charged during key C–C or C–N bond formation for emitter core construction
    • Treated with scavenging agents and CSP filtration prior to work-up
    • Residual catalyst levels monitored to <10 ppm prior to final formulation

    Final product types

    • OLED emitter molecules (e.g., phosphorescent dopants)
    • Conductive polymers for display applications
    • Intermediate arylamine ligands for further downstream modification

    3. Agrochemical Intermediate Synthesis

    Manufacturers in the crop protection and agro-intermediate industry utilize this catalyst to enable construction of biaryl scaffolds and nitrogen heterocycles in new-generation fungicide and insecticide cores. Plants follow strict trace metal control and residue removal validated against FAO and EPA regulatory maximums for technical-grade products. Catalyst charge is selected based on substrate complexity, desired turnover, and environmental controls for palladium limits. The material enters the process during the arylation stage, followed by aggressive work-up and adsorption treatments to ensure metal removal. This supports downstream formulation of agrochemicals with compliant impurity profiles.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • US EPA Pesticide Residue Tolerances (40 CFR Part 180)
    • ISO 9001 Quality System (for technical manufacturing)

    Typical usage ratio

    • 0.05–0.5 mol% of catalyst with respect to the aryl halide or heterocyclic substrate; balanced for cost and residual levels

    Downstream process integration

    • Added to main reactor with ligands and base at the C–C or C–N forming step
    • Aggressive adsorptive work-up after reaction, followed by in-process residual metal QC
    • Ensures final intermediate meets agrochemical registration standards

    Final product types

    • Technical-grade fungicide and insecticide intermediates
    • Key scaffolds for formulation into finished crop protection agents

    4. Specialty Polymer Synthesis: Advanced Polyaromatic Materials

    Producers of high-performance specialty polymers, such as conjugated polyarylenes for advanced membranes and sensor devices, select this catalyst to catalyze C–C coupling in the construction of extended π-conjugated frameworks. Process engineers operate under stringent industry-specific environmental, health, and worker-safety requirements, particularly concerning heavy metal residues and solvent holdup. Usage ratios reflect the monomer reactivity and the desired molecular weight distribution of the resulting polymer. The material enters the synthesis at the main backbone construction phase, typically under Schlenk or inert atmosphere operations. Downstream, rigorous purification via Soxhlet extraction or solid-phase scavenging ensures finished polymer purity.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 (for chemical management in EU)
    • ISO 9001 Quality Assurance (specialty chemical production)
    • OSHA 29 CFR 1910 (Worker Safety, US)

    Typical usage ratio

    • 0.05–1 mol% relative to each monomer; defined by polymerization degree and expected catalyst turnover

    Downstream process integration

    • Added during Grignard metathesis polycondensation or direct arylation polymerization
    • Polymer and catalyst separated by solvent extraction or precipitation methods
    • Routine residual Pd testing prior to material qualification

    Final product types

    • Conjugated polyarylenes for electronic sensors
    • High-purity polymeric membranes for filtration sectors
    • Specialty materials for optoelectronic components
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