Bis(ethylenediamine)palladium(II) Dichloride TCI B2244

Chemical Identity

CAS No.: 16483-18-4
PubChem: CID 167543·SID 87565097
Formula: C4H16Cl2N4Pd
Molecular weight: 297.52 g/mol
Purity: >98.0%(T)
Reference databases: ECHA

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: bis(ethane-1,2-diamine);palladium(2+);dichloride
SMILES: C(CN)N.C(CN)N.[Cl-].[Cl-].[Pd+2]
InChIKey: VBDQNUWZQXYUDP-UHFFFAOYSA-L

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Bis(ethylenediamine)palladium(II) Dichloride is a chemical compound widely used in catalytic reactions, particularly in organic synthesis. As a transition metal complex, it plays a crucial role in accelerating chemical reactions without being consumed in the process. This compound is especially effective in coupling reactions, such as the Suzuki-Miyaura and Heck reactions, where it facilitates the formation of carbon-carbon bonds. Its versatility makes it an essential tool for chemists working in both organic and inorganic fields.

The compound is prized for its high catalytic activity and stability under various reaction conditions. Its ability to bind with different ligands allows for precise control over reaction environments, making it highly adaptable to a range of synthetic strategies. Additionally, its relatively stable nature ensures that it remains effective over time, reducing the need for frequent replenishment. These properties make it a preferred choice for researchers aiming to achieve efficient and reproducible results in their experiments.

In Indonesian laboratories, Bis(ethylenediamine)palladium(II) Dichloride is commonly used in organic chemistry research, particularly in the synthesis of complex organic molecules. Its role in catalytic processes is vital for advancing chemical studies and developing new compounds. Due to its effectiveness and reliability, it is a staple in many research settings, supporting both academic and industrial applications.

TCI brochures (PDF)

Transition Metal Catalysts 2026-04-10 · p. 14

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Organic synthesis reactions benefit from its catalytic activity in forming carbon-carbon bonds efficiently.
Transition metal catalysis applications rely on its stability and ability to coordinate with various ligands.
Coupling reactions such as Suzuki-Miyaura and Heck are enhanced by its high reactivity and selectivity.
Inorganic chemistry experiments use it to study metal-ligand interactions and coordination chemistry.
Catalytic processes in industrial-scale chemical production require its reliability and consistent performance.

Brand	TCI
CAS number	16483-18-4
Molecular formula	—
Purity	—
Category	Chemistry > Catalysis and Inorganic Chemistry > Transition Elements [Catalysis and Inorganic Chemistry]
Pack sizes	Available in various quantities as per standard laboratory supply
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, away from moisture and direct sunlight to maintain its stability. It is recommended to use airtight containers to prevent exposure to air and humidity. Since it is a catalyst, it should be handled with care to avoid contamination. Proper labeling of containers is essential for safe storage and retrieval. Laboratory personnel should wear appropriate personal protective equipment when handling it to ensure safety. Regular inspection of storage conditions is advised to ensure the compound remains in optimal condition for use.

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