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Merck

267112

Palladium

wire, diam. 1.0 mm, 99.9% trace metals basis

Synonym(s):

Palladium (powder), Palladium black, Palladium element

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900 MG

€ 265,00

9 G

€ 2.280,00

€ 265,00

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About This Item

Linear Formula:
Pd
CAS Number:
7440-05-3
Molecular Weight:
106.42
NACRES:
NA.23
PubChem Substance ID:
24856199
UNSPSC Code:
12141733
EC Number:
231-115-6
MDL number:
MFCD00011167

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Product Name

Palladium, wire, diam. 1.0 mm, 99.9% trace metals basis

InChI key

KDLHZDBZIXYQEI-UHFFFAOYSA-N

InChI

1S/Pd

SMILES string

[Pd]

assay

99.9% trace metals basis

form

wire

resistivity

9.96 μΩ-cm, 20°C

diam.

1.0 mm

bp

2970 °C (lit.)

mp

1554 °C (lit.)

density

12.02 g/cm3 (lit.)

Quality Level

100

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1 of 4

This Item
348694GF65941421348678
Palladium wire, diam. 1.0 mm, 99.9% trace metals basis

Sigma-Aldrich

267112

Palladium

Palladium wire, diam. 0.5 mm, 99.9% trace metals basis

Sigma-Aldrich

348694

Palladium

Palladium wire, 0.04 mm diameter, length 1 m, purity 99.95%

GF65941421

Palladium

Palladium foil, thickness 1.0 mm, 99.9% trace metals basis

Sigma-Aldrich

348678

Palladium

assay

99.9% trace metals basis

assay

99.9% trace metals basis

assay

99.95%

assay

99.9% trace metals basis

form

wire

form

wire

form

wire

form

foil

mp

1554 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (lit.)

mp

1554 °C (lit.)

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.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

density

12.02 g/cm3 (lit.)

Application

Palladium is widely used as a metal wire electrode to synthesize Pd-based nanomaterials with good electrocatalytic activity. For example, it is used to prepare carbon-supported Pd nanoclusters and PdAu nanoparticles.

Itcan also be used as a hydrogenation catalyst in various organic reactions, suchas hydrogenation of alkenes and alkynes to their corresponding hydrocarbons.

Preparation Note

900 mg = 10 cm; 9 g = 100 cm

Storage Class

13 - Non Combustible Solids

wgk

WGK 3

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Eyeshields, Gloves, type N95 (US)

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Certificates of Analysis (COA)

Lot/Batch Number
MKCV2963
MKCR6186
MKCS1493
MKCQ9071
MKCP7723

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Ling Li et al.
Nature chemistry, 5(7), 607-612 (2013-06-22)
The development of transition metal-catalysed cross-coupling reactions has greatly influenced the manner in which the synthesis of complex organic molecules is approached. A wide variety of methods are now available for the formation of C(sp(2))-C(sp(2)) bonds, and more recent work
Gary A Molander et al.
The Journal of organic chemistry, 78(8), 4123-4131 (2013-04-11)
A method has been developed for the Pd-catalyzed synthesis of α-(hetero)aryl esters and amides through a Suzuki-Miyaura cross-coupling reaction. This method avoids the use of strong base, does not necessitate inert or low temperature formation of reagents, and does not
A K Grekhova et al.
Biomeditsinskaia khimiia, 59(1), 107-114 (2013-05-09)
A comparative study on the genotoxic activity of cisplatin versus morfozol, the first representative of a new class of cation-anion complexes of palladium [AH]2[PdCl4] (where A-methylmorpholine) has been performed using human lymphocytes in vitro. The results of the DNA-DNA cross-linking
Sylwester Kurcoń et al.
The Journal of organic chemistry, 78(8), 4115-4122 (2013-04-03)
Heptamethyl cobyrinate was transformed into hexamethyl 8-nor-cobyrinate. The crucial step involved the synthesis of new, vitamin B12 derived cobryketone via palladium-catalyzed cleavage of the sp(3)-sp(3) carbon-carbon bond with the liberation of the ketone. The replacement of sp(3) carbon atom with
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.
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