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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 | 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. |
Applications of Bis(Tri-Tert-Butylphosphine)Palladium(0) in Industrial ManufacturingAs 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 SynthesisMajor 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
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2. Electronic Materials: OLED Intermediate SynthesisProducers 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
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3. Agrochemical Intermediate SynthesisManufacturers 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
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4. Specialty Polymer Synthesis: Advanced Polyaromatic MaterialsProducers 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
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