Bis(triphenylphosphine)palladium(II) Dichloride TCI B1667

Chemical Identity

Other names: [PdCl2(PPh3)2]
CAS No.: 13965-03-2
PubChem: CID 84124·SID 87564568
Formula: C36H30Cl2P2Pd
Molecular weight: 701.9 g/mol
Purity: >98.0%(T)
Reference databases: ChemSpider·ECHA·Wikipedia

Full identifiers (IUPAC, SMILES, InChIKey)

IUPAC: palladium(2+);bis(triphenylphosphane);dichloride
SMILES: C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.C1=CC=C(C=C1)P(C2=CC=CC=C2)C3=CC=CC=C3.[Cl-].[Cl-].[Pd+2]
InChIKey: YNHIGQDRGKUECZ-UHFFFAOYSA-L

Rp 1.618.050,00

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Bis(triphenylphosphine)palladium(II) Dichloride is a chemical compound widely used in catalytic reactions, particularly in C-H activation processes. It plays a crucial role in the synthesis of complex organic compounds, such as in coupling and substitution reactions. As a catalyst, it accelerates chemical reactions without being consumed in the final product. This compound is essential in modern laboratory settings where efficiency and selectivity are paramount. Its unique properties make it a versatile tool for chemists working in both organic and inorganic chemistry.

The compound is known for its chemical stability and high reactivity towards transition metal reactions. It has the ability to bind with other ligands, which enhances its applicability in various chemical reactions. This property allows it to be used in a wide range of catalytic processes, making it a preferred choice for researchers. Its compatibility with different reaction conditions and its effectiveness in promoting desired chemical transformations further solidify its importance in laboratory work.

In Indonesian laboratories, Bis(triphenylphosphine)palladium(II) Dichloride is commonly used in organic and inorganic chemistry research. Its availability and reliable performance make it a sought-after material for students and researchers conducting catalytic experiments. Its role in enabling efficient and selective reactions is vital for advancing chemical studies in Indonesia.

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

C-H Activation Reactions: This compound is ideal for activating carbon-hydrogen bonds, enabling selective functionalization in complex organic molecules.
Cross-Coupling Reactions: Its catalytic properties make it suitable for cross-coupling reactions, such as Suzuki or Heck reactions, where bond formation between different organic substrates is required.
Substitution Reactions: It is frequently used in substitution reactions to replace hydrogen atoms with other functional groups, enhancing the versatility of synthetic pathways.
Transition Metal Catalysis: Due to its interaction with transition metals, it is a key component in catalytic systems involving metal-based reactions.
Ligand Binding Studies: Its ability to bind with other ligands makes it useful in studying coordination chemistry and ligand exchange processes.

Brand	TCI
CAS number	13965-03-2
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
Storage	Store in a cool, dry place away from moisture and light

This compound should be stored in a cool, dry environment, away from moisture and direct light to maintain its stability and reactivity. It is recommended to use airtight containers to prevent exposure to air and humidity. Due to its chemical nature, it should be handled with care, using appropriate personal protective equipment such as gloves and safety goggles. It is important to ensure that the storage area is well-ventilated to minimize any potential risks associated with its handling. Proper labeling of containers is also essential to ensure safe and efficient use in laboratory settings.

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