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348678

Sigma-Aldrich

Palladium

foil, thickness 1.0 mm, 99.9% trace metals basis

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Synonym(s):
Palladium (powder), Palladium black, Palladium element
Linear Formula:
Pd
CAS Number:
Molecular Weight:
106.42
EC Number:
MDL number:
PubChem Substance ID:
NACRES:
NA.23

Quality Level

Assay

99.9% trace metals basis

form

foil

resistivity

9.96 μΩ-cm, 20°C

thickness

1.0 mm

bp

2970 °C (lit.)

mp

1554 °C (lit.)

density

12.02 g/cm3 (lit.)

SMILES string

[Pd]

InChI

1S/Pd

InChI key

KDLHZDBZIXYQEI-UHFFFAOYSA-N

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1 of 4

This Item
348643267120464651
Palladium foil, thickness 1.0 mm, 99.9% trace metals basis

Sigma-Aldrich

348678

Palladium

Palladium foil, thickness 0.25 mm, 99.98% trace metals basis

Sigma-Aldrich

348643

Palladium

Palladium foil, thickness 0.025 mm, 99.9% trace metals basis

Sigma-Aldrich

267120

Palladium

Palladium powder, <75 μm, 99.9% trace metals basis

Sigma-Aldrich

464651

Palladium

form

foil

form

foil

form

foil

form

powder

resistivity

9.96 μΩ-cm, 20°C

resistivity

9.96 μΩ-cm, 20°C

resistivity

9.96 μΩ-cm, 20°C

resistivity

9.96 μΩ-cm, 20°C

bp

2970 °C (lit.)

bp

2970 °C (lit.)

bp

2970 °C (lit.)

bp

2970 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

General description

Palladium and its alloys are used for hydrogen purification in fuel cells. Energy dispersive x-ray diffraction during electrochemical loading of palladium foils with hydrogen and deuterium was studied. Palladium foil was tested as a catalyst for Suzuki-Miyaura cross coupling reaction.

Quantity

7.6 g = 25 × 25 mm; 30.4 g = 50 × 50 mm

Storage Class Code

13 - Non Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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25G
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MMYOMAG-74K-13

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Studies on the catalytic ability of palladium wire, foil and sponge in the Suzuki-Miyaura cross coupling
Amoroso F, et al.
Inorgorganica Chimica Acta, 375, 256-262 (2011)
In situ synchrotron energy-dispersive x-ray diffraction study of thin Pd foils with Pd:D and Pd:H concentrations up to 1:1
Knies DL, et al.
Journal of Applied Physics, 112 (2012)
Xuxing Chen et al.
Organic & biomolecular chemistry, 11(16), 2582-2585 (2013-03-19)
A one-pot two-step synthesis of versatile indenones has been developed. This palladium(II)-catalyzed transformation involves generation and condensation of ortho-functionalized 1,2-benzils from 2-(2-arylethynylphenyl)acetonitriles using Ph2SO as the oxidant. The resulting 3-cyanoindenones can be converted to various valuable molecules.
Stefano Nicolai et al.
The Journal of organic chemistry, 78(8), 3783-3801 (2013-03-21)
Tetrahydrofurans and pyrrolidines are among the most important heterocycles found in bioactive compounds. Cyclization-functionalization domino reactions of alcohols or amines onto olefins constitute one of the most efficient methods to access them. In this context, oxy- and aminoalkynylation are especially
Meng Wang et al.
Organic & biomolecular chemistry, 11(16), 2574-2577 (2013-03-15)
A novel Pd/Cu catalyzed domino reaction for the synthesis of functionalized pyrrolo[1,2-b]pyridazines from readily accessible (hetero)aryl propargyl alcohols and 1-amino-2-bromopyrroles was developed. This cascade process involves a Sonogashira cross-coupling reaction, an isomerization and an intramolecular condensation.

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