This material is a metal-based complex compound containing palladium, widely used in catalytic reactions, particularly in organic synthesis. As a palladium-based catalyst, it plays a crucial role in accelerating chemical reactions while maintaining stability and selectivity. Its application spans various fields of chemistry, including both organic and inorganic research, where efficiency and precision are essential. The compound is part of the imidazole-based catalyst category, known for its ability to mediate complex reactions such as coupling, hydroformylation, and hydrogenation.
The compound's unique structure, consisting of a palladium(II) ion coordinated with imidazole and acetanilide ligands, provides it with high catalytic activity and stability. These properties make it a preferred choice for researchers aiming to achieve consistent and reproducible results in their experiments. Its chemical and physical properties are well-suited for use in controlled laboratory environments, ensuring reliable performance under various reaction conditions.
In Indonesian laboratories, this compound is commonly used in organic chemistry research, especially in catalytic reactions requiring efficient and selective catalysts. It is also employed in the development of environmentally friendly and cost-effective synthetic methods. Due to its specific properties, it is a valuable tool for advancing chemical research and innovation in the region.
TCI brochures (PDF)
- Palladium Catalyst with Both Ease-of-Handling and High Reactivity 2025-01-06 · p. 1
- Useful Palladacycle Catalysts 2025-04-17 · p. 1
- N-Heterocyclic Carbene (NHC) Ligands and Metal Complexes 2026-02-10 · p. 2
- Transition Metal Catalysts 2026-04-10 · p. 14
- Suzuki-Miyaura Cross Coupling Reaction 2025-12-01 · p. 23
Related TCI products
- TCI C2406 1093348-08-3 Chloro[[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](N,N-dimethyl-3,5-dimethoxybenzylamine)palladium(II)]
- TCI C2372 930796-10-4 Chloro[[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](N,N-dimethylbenzylamine)palladium(II)]
- TCI B6199 905459-27-0 [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) Dichloride
- TCI D3806 287410-78-0 Di-mu-chlorobis[5-chloro-2-[(4-chlorophenyl)(hydroxyimino)methyl]phenyl]palladium(II) Dimer
- TCI C2734 1375325-71-5 Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II)
- TCI T1350 14221-01-3 Tetrakis(triphenylphosphine)palladium(0)
- Organic synthesis reactions benefit from this catalyst’s ability to mediate coupling and hydrogenation processes efficiently.
- Catalytic hydrogenation applications rely on its stability and selectivity to ensure consistent product formation.
- Hydroformylation reactions utilize its high activity to enhance the rate of carbon-carbon bond formation.
- Inorganic chemistry research leverages its structural complexity for studying transition metal coordination chemistry.
- Green chemistry initiatives incorporate this compound to develop sustainable and eco-friendly synthetic pathways.
From the TCI brochure
- Highly active Suzuki-Miyaura coupling catalyst
| Brand | TCI |
|---|---|
| CAS number | 1228009-69-5 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Catalysis and Inorganic Chemistry > Transition Elements [Catalysis and Inorganic Chemistry] |
| Pack sizes | Available in standard laboratory quantities as per supplier specifications |
| Physical form | Solid powder or crystalline form, depending on packaging |
| 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 chemical integrity and catalytic activity. It is recommended to use airtight containers to prevent exposure to moisture and air, which could lead to degradation. Due to its chemical nature, it should be handled with appropriate personal protective equipment, such as gloves and safety goggles, to ensure laboratory safety. Avoid direct contact with skin or inhalation of vapors. It is important to keep the material away from incompatible substances and ensure proper ventilation in the workspace. Regular monitoring of storage conditions will help preserve the compound's effectiveness for research applications.
—
Product Categories
- Catalysis and Inorganic ChemistryTransition Elements [Catalysis and Inorganic Chemistry]Palladium [Catalysis and Inorganic Chemistry]
- Catalysis and Inorganic ChemistryCross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]Palladium Catalysts [Cross-coupling Reaction using Transition Metal Catalysts]
- Synthetic ReagentsC-C Bond Formation [Synthetic Reagents]Cross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]
palladium(II)] (CAS 1228009-69-5) - TCI C2387 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510C2387.jpg?v=1767098252&width=1445)
palladium(II)] (CAS 1093348-08-3) - TCI C2406 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510C2406.jpg?v=1767098294&width=533)
palladium(II)] (CAS 930796-10-4) - TCI C2372 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510C2372.jpg?v=1767098223&width=533)
palladium(II) Dichloride (CAS 905459-27-0) - TCI B6199 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510B6199_8fb24a5d-0ce1-4fc9-b0bc-4be9be705d27.jpg?v=1767864859&width=533)
![Di-mu-chlorobis[5-chloro-2-[(4-chlorophenyl)(hydroxyimino)methyl]phenyl]palladium(II) Dimer (CAS 287410-78-0) - TCI D3806 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510D3806.jpg?v=1767106583&width=533)
![Chloro[(tri-tert-butylphosphine)-2-(2-aminobiphenyl)]palladium(II) (CAS 1375325-71-5) - TCI C2734 - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510C2734.jpg?v=1767098705&width=533)

![31277-98-2 Bis[1,2-bis(diphenylphosphino)ethane]palladium(0) - AMI Scientific](http://amiscientific.com/cdn/shop/files/TCI2510B3224_8c85b882-6dd5-4a37-880a-a8e8601dc8ca.jpg?v=1767431836&width=533)
