Palladium(II) Acetate (Purified), with the CAS number 3375-31-3, is a key chemical compound widely used in catalytic processes, particularly in C-H activation reactions. This compound serves as an essential catalyst in various chemical reactions, enabling the efficient transformation of organic molecules without being consumed in the process. It is commonly found in chemical laboratories, especially in fields like catalysis and inorganic chemistry, where its reactivity and effectiveness are highly valued. As a versatile catalyst, Palladium(II) Acetate plays a critical role in facilitating complex chemical transformations, making it a fundamental reagent in modern synthetic chemistry.
One of the primary reasons Palladium(II) Acetate is preferred in laboratory settings is its high reactivity and stability. It exhibits excellent solubility in organic solvents, which makes it easy to handle and incorporate into various reaction systems. Its chemical structure allows it to act as an efficient catalyst in a wide range of reactions, including hydrogenation, oxidation, and substitution reactions. Additionally, its ability to selectively activate C-H bonds makes it particularly useful in synthetic applications where specificity is crucial. These properties contribute to its widespread use in both academic and industrial research environments.
In Indonesian laboratories, Palladium(II) Acetate is frequently utilized in chemical research, especially in catalysis and organic synthesis. Its role in accelerating chemical reactions with high efficiency has made it a preferred choice for researchers aiming to optimize reaction conditions and reduce the need for excessive reagents. Its availability and performance make it a standard component in many chemical laboratories across Indonesia, supporting both basic and applied research in the field of chemistry.
TCI brochures (PDF)
- Carbon Monoxide (CO) Surrogate Reagents for Carbonylation 2024-11-07 · p. 2
- Easily-preparable N-Heterocyclic Carbene (NHC) Precursors 2021-09-14 · p. 1
- Sulfur Dioxide (SO2) Surrogate Reagents Usable for Sulfonation 2026-05-18 · p. 1
- Palladium Catalysts for Cross-Coupling Reaction 2025-05-01 · p. 1
- Oxidizing Agents 2025-06-11 · p. 9
- C-H Bond Activation Reaction 2025-06-20 · p. 4
Related TCI products
- TCI A1424 3375-31-3 Palladium(II) Acetate
- TCI P1870 42196-31-6 Palladium(II) Trifluoroacetate
- TCI P1489 7647-10-1 Palladium(II) Chloride
- TCI T1350 14221-01-3 Tetrakis(triphenylphosphine)palladium(0)
- TCI B3160 95408-45-0 [1,1'-Bis(di-tert-butylphosphino)ferrocene]palladium(II) Dichloride
- TCI B2064 95464-05-4 [1,1'-Bis(diphenylphosphino)ferrocene]palladium(II) Dichloride Dichloromethane Adduct
- C-H Activation Reactions: Palladium(II) Acetate is ideal for C-H activation due to its ability to selectively activate carbon-hydrogen bonds, enabling efficient and targeted chemical transformations.
- Organic Synthesis: This compound is widely used in organic synthesis to facilitate complex reactions with high yield and selectivity, making it a valuable tool in synthetic chemistry.
- Catalytic Hydrogenation: Its catalytic properties make it suitable for hydrogenation reactions, where it helps in the reduction of organic compounds under controlled conditions.
- Oxidation Reactions: Palladium(II) Acetate can be used in oxidation processes to promote the formation of functional groups in organic molecules.
- Substitution Reactions: It is effective in substitution reactions, where it facilitates the replacement of specific atoms or groups in organic compounds.
From the TCI brochure
- Metal reactant for Pd(NHC)3(OAc)2 preparation with NHC-CO2 adducts
| Brand | TCI |
|---|---|
| CAS number | 3375-31-3 |
| Molecular formula | — |
| Purity | — |
| Category | Chemistry > Catalysis and Inorganic Chemistry > C-H Activation [Catalysis] |
| Pack sizes | Available in various quantities as per supplier specifications |
| Physical form | Solid (may vary depending on supplier) |
| Storage | Store in a cool, dry place away from moisture and light |
Palladium(II) Acetate should be stored in a cool, dry environment to maintain its chemical stability and prevent degradation. It is recommended to keep the compound in a sealed container to minimize exposure to moisture and air, which can affect its reactivity. When handling this material, it is important to use appropriate personal protective equipment, such as gloves and safety goggles, to avoid direct contact. Due to its chemical nature, it should be stored away from incompatible substances like strong acids or bases. In laboratory settings, it is essential to follow standard safety protocols to ensure safe handling and prevent any potential hazards. Proper storage and handling practices help preserve the compound's effectiveness and ensure its safe use in chemical experiments.
References cited in the TCI brochure
- Adelina M. Voutchkova. Disubstituted Imidazolium-2-Carboxylates as Efficient Precursors to N-Heterocyclic Carbene Complexes of Rh, Ru, Ir, and Pd Journal of the American Chemical Society, 2005. doi:10.1021/ja056625k
Product Categories
- Catalysis and Inorganic ChemistryC-H Activation [Catalysis]Palladium Compounds [C-H Activation]
- Catalysis and Inorganic ChemistryOxidation [Catalysis]Metal Catalysts for Oxidation
- 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]
- Catalysis and Inorganic ChemistryMetallic Salts [Catalysis and Inorganic Chemistry]Acetate Salts [Metallic Salts]
- Synthetic ReagentsC-C Bond Formation [Synthetic Reagents]Cross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]
