1,4-Bis(diphenylphosphino)butane palladium(II) dichloride is a versatile catalyst widely used in chemical reactions, particularly in C-H activation processes. This compound plays a crucial role in laboratory settings where metal-based catalysts are required for the synthesis of complex organic compounds. Its ability to facilitate selective and efficient chemical transformations makes it an essential reagent in modern synthetic chemistry. It is especially valuable in reactions that demand high catalytic activity and specificity, contributing to the advancement of both academic and industrial research.
The compound's unique molecular structure and strong affinity for metal atoms make it a preferred choice among chemists. Its stability under various reaction conditions and its capacity to form active catalytic species enhance its effectiveness in a wide range of applications. Additionally, its resistance to unwanted side reactions ensures minimal contamination, which is critical in maintaining the integrity of experimental results. These properties collectively contribute to its reliability and performance in both research and production environments.
In Indonesian laboratories, this catalyst is commonly used in research focused on organic synthesis, catalytic processes, and material science. Its application is particularly prominent in studies involving cross-coupling reactions and hydrogenation processes. Due to its high efficiency and cost-effectiveness, it is a favored option for researchers aiming to optimize reaction outcomes while maintaining experimental consistency.
TCI brochures (PDF)
- Palladium Catalysts for Cross-Coupling Reaction 2025-05-01 · p. 1
- C-H Bond Activation Reaction 2025-06-20 · p. 4
- Transition Metal Catalysts 2026-04-10 · p. 14
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 23
Related TCI products
- TCI B3160 95408-45-0 [1,1'-Bis(di-tert-butylphosphino)ferrocene]palladium(II) Dichloride
- TCI B2192 59831-02-6 [1,3-Bis(diphenylphosphino)propane]palladium(II) Dichloride
- TCI B2064 95464-05-4 [1,1'-Bis(diphenylphosphino)ferrocene]palladium(II) Dichloride Dichloromethane Adduct
- TCI B2055 29934-17-6 Bis(tricyclohexylphosphine)palladium(II) Dichloride
- TCI B2026 40691-33-6 Bis(tri-o-tolylphosphine)palladium(II) Dichloride
- TCI B2016 19978-61-1 [1,2-Bis(diphenylphosphino)ethane]palladium(II) Dichloride
- C-H Activation Reactions: This catalyst is ideal for C-H activation due to its ability to facilitate selective bond cleavage and formation, enhancing reaction efficiency.
- Cross-Coupling Reactions: It is widely used in cross-coupling reactions because of its high catalytic activity and compatibility with various substrates.
- Hydrodefunctionalization Processes: The compound supports hydrodefunctionalization by enabling efficient hydrogenation under mild conditions.
- Organic Synthesis in Industrial Settings: Its stability and reusability make it suitable for large-scale organic synthesis in industrial laboratories.
- Material Science Research: It is employed in the development of new materials due to its ability to promote controlled chemical transformations.
| Brand | TCI |
|---|---|
| CAS number | 29964-62-3 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis] |
| Pack sizes | Available in various quantities as per standard laboratory requirements |
| Physical form | Solid powder |
| Storage | Store in a cool, dry place away from moisture and direct sunlight |
This compound should be stored in a cool, dry environment to maintain its stability and catalytic activity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could degrade its performance. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is advisable to store it in a well-ventilated area to minimize any potential risks associated with its handling. Proper storage ensures that the material remains effective for extended periods, supporting consistent results in laboratory experiments.
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