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Sigma-Aldrich

Potassium tetrachloropalladate(II)

98%

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Synonym(s):
Potassium palladium(II) chloride
Linear Formula:
K2PdCl4
CAS Number:
Molecular Weight:
326.43
EC Number:
MDL number:
UNSPSC Code:
12352302
PubChem Substance ID:
NACRES:
NA.23

Quality Level

assay

98%

form

crystals

mp

105 °C (dec.) (lit.)

density

2.67 g/mL at 25 °C (lit.)

SMILES string

[K+].[K+].Cl[Pd--](Cl)(Cl)Cl

InChI

1S/4ClH.2K.Pd/h4*1H;;;/q;;;;2*+1;+2/p-4

InChI key

LGCKLDWLSVFMGL-UHFFFAOYSA-J

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General description

Potassium tetrachloropalladate(II) is a dark brown crystalline solid widely used as a Pd source in the field of catalysis, nanomaterial synthesis, and electronics.

Application

Potassium tetrachloropalladate(II) can be used:
  • As a precursor to synthesize Pd nanoparticles for catalytic degradation of organic pollutants and Pd-GO electrocatalyst in formic acid and ethanol oxidation.
  • To synthesize Pd–Pt alloy nanocrystals (NCs) with hollow structures by a galvanic replacement method with uniform Pd octahedral and cubic NCs as sacrificial templates. The hollow NCs exhibited higher ORR activities.
  • To synthesize immobilized Pd catalysts, a versatile method involves the layer-by-layer deposition of PAA and PEI-Pd(II) on alumina, followed by the reduction of Pd2+. This approach offers several benefits, including the stabilization of particles through the polyelectrolyte matrix, introduction of selectivity, and a significant reduction in undesired isomerization. Expanding the application of polyelectrolyte films holds promise for further enhancing selectivity in hydrogenation and other reactions.
  • To fabricate conductive and porous metal-organic frameworks(MOFs) for gas sensing applications and also to synthesize bimetallic Pd/SnO2 nanoparticles on metal organic framework (MOF) as an electrocatalyst for ethanol oxidation.
  • To prepare rigid macrocyclic pincer catalysts possessing polyaromatic ligands with enhanced catalytic activity.

Features and Benefits

Used in the synthesis of semiconducting metal-containing polymers in which the polypyrrole backbone has a conformational energy minimum and is nearly planar. Reacts with bis(dithiolates) to metal-bis(dithiolates) with applications in laser Q-switch materials, optical CD recording media, bar code material and superconductivity.

Pictograms

Exclamation mark

signalword

Warning

Hazard Classifications

Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3

target_organs

Respiratory system

wgk_germany

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

dust mask type N95 (US), Eyeshields, Gloves


Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Mathis, M. et al.
Chemistry of Materials, 10, 3568-3568 (1998)
L V Tat'ianenko et al.
Voprosy meditsinskoi khimii, 28(6), 126-131 (1982-11-01)
Mechanism of interaction between biologically active substances and membranes as well as and membrane-bound enzymes of two types: mitochondrial monoamine oxidase (MAO) from rat liver tissue and Ca2+, Mg+2-dependent ATPase from sarcoplasmic reticulum (SR) were studied. All the substances studied
Joris Muris et al.
Contact dermatitis, 67(2), 94-100 (2012-04-03)
Exposure to palladium (Pd) may lead to clinical allergic reactions. With frequent nickel (Ni) exposure and cross-reactivity between Ni and Pd at the T cell recognition level, positive Pd reactions on patch testing are surprisingly uncommon. PdCl(2) is often used
B L Iverson et al.
Nucleic acids research, 15(19), 7823-7830 (1987-10-12)
Reaction of DNA with K2PdCl4 at pH 2.0 followed by a piperidine workup produces specific cleavage at adenine (A) residues. Product analysis revealed the K2PdCl4 reaction involves selective depurination at adenine, affording an excision reaction analogous to the other chemical
[Spectrophotometric analysis of D-penicillamine and mercaptopropionylglycine in pharmaceutical formulations with ammonium tetrachloropalladate].
M A Raggi et al.
Bollettino chimico farmaceutico, 125(8), 295-297 (1986-08-01)

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