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686468

Sigma-Aldrich

Palladium

nanopowder, <25 nm particle size (TEM), ≥99.5%

Sinonimo/i:

Palladium (powder), Palladium black, Palladium element

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About This Item

Formula condensata:
Pd
Numero CAS:
7440-05-3
Peso molecolare:
106.42
Numero CE:
231-115-6
Numero MDL:
MFCD00011167
Codice UNSPSC:
12352302
ID PubChem:
329761051
NACRES:
NA.23

Livello qualitativo

100

Saggio

≥99.5%

Forma fisica

nanopowder

Impiego in reazioni chimiche

reagent type: catalyst
core: palladium

Resistività

9.96 μΩ-cm, 20°C

Dimensione particelle

<25 nm (TEM)

P. eboll.

2970 °C (lit.)

Punto di fusione

1554 °C (lit.)

Densità

12.02 g/cm3 (lit.)

applicazioni

battery manufacturing

Stringa SMILE

[Pd]

InChI

1S/Pd
KDLHZDBZIXYQEI-UHFFFAOYSA-N

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Pittogrammi

FlameExclamation mark
GHS02,GHS07

Avvertenze

Danger

Indicazioni di pericolo

H228,H315,H319,H335

Classi di pericolo

Eye Irrit. 2 - Flam. Sol. 1 - Skin Irrit. 2 - STOT SE 3

Organi bersaglio

Respiratory system

Codice della classe di stoccaggio

4.1B - Flammable solid hazardous materials

Classe di pericolosità dell'acqua (WGK)

WGK 3

Punto d’infiammabilità (°F)

Not applicable

Punto d’infiammabilità (°C)

Not applicable

Dispositivi di protezione individuale

Eyeshields, Gloves, type P3 (EN 143) respirator cartridges

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Certificati d'analisi (COA)

Lot/Batch Number
MKCP7211
MKCM3115
MKCL3042
MKCH7939
MKCD2756

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Palladium powder, &lt;75&#160;&#956;m, 99.9% trace metals basis

Sigma-Aldrich

464651

Palladium

Palladium powder, max. particle size 10 micron, weight 1&#160;g, purity 99.95%

GF05003693

Palladium

Palladium 99+ powdered for analysis 99+ EMSURE&#174;

Supelco

1.19225

Palladium 99+ powdered

Palladium sponge, 99.9% trace metals basis

Sigma-Aldrich

267082

Palladium

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.
Meifang Zheng et al.
Organic letters, 15(8), 1838-1841 (2013-04-02)
Palladium-catalyzed oxidative difunctionalization of enol ethers with 1,3-dicarbonyl compounds to construct trisubstituted furans in one step under mild conditions is described. The reaction is thought to proceed through a C-C bond formation along with a C-O bond closing the ring
Bin Kim et al.
Journal of nanoscience and nanotechnology, 13(1), 517-522 (2013-05-08)
In order to form flexible printed circuits through inkjet printing technique, the Pd(ll) catalyst ink was printed on the surface of polyimide film modified with KOH solution and then reduced with NaBH4 solution to extract the Pd(O) catalyst nuclei. The
Xiaohu Xia et al.
Proceedings of the National Academy of Sciences of the United States of America, 110(17), 6669-6673 (2013-04-10)
Controlling the shape or morphology of metal nanocrystals is central to the realization of their many applications in catalysis, plasmonics, and electronics. In one of the approaches, the metal nanocrystals are grown from seeds of certain crystallinity through the addition
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
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