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205680

Sigma-Aldrich

Palladium on carbon

greener alternative

extent of labeling: 5 wt. % loading (dry basis), matrix activated carbon support

Synonym(s):

Pd/C

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About This Item

Linear Formula:
Pd
Molecular Weight:
106.42
MDL number:
MFCD03457879
UNSPSC Code:
12141733
eCl@ss:
38191001
PubChem Substance ID:
24852218
NACRES:
NA.22

form

powder

reaction suitability

core: palladium
reaction type: Buchwald-Hartwig Cross Coupling Reaction
reaction type: Heck Reaction
reaction type: Hiyama Coupling
reaction type: Negishi Coupling
reaction type: Sonogashira Coupling
reaction type: Stille Coupling
reaction type: Suzuki-Miyaura Coupling
reagent type: catalyst

greener alternative product characteristics

Design for Energy Efficiency
Learn more about the Principles of Green Chemistry.

sustainability

Greener Alternative Product

extent of labeling

5 wt. % loading (dry basis)

matrix

activated carbon support

greener alternative category

Enabling,

SMILES string

[Pd]

InChI

1S/Pd

InChI key

KDLHZDBZIXYQEI-UHFFFAOYSA-N

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General description

We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find details here.

Application

Catalyst for:
  • Stille reaction
  • Hydrogenation reactions
  • Suzuki-Miyaura cross-coupling and Heck-Mizoroki reactions
  • Deoxygenation
  • Oxidation reactions
  • Coupling reactions
Palladium on carbon (Pd/C) (5 wt. % loading (dry basis), matrix activated carbon support) can be used for a variety of applications, such as:

  • a catalyst for hydrodechlorination of dichlorodifluoromethane (CCl2F2), which is a known greenhouse gas
  • a catalyst for Heck reactions of aryl halides in ionic liquids
  • an anode catalyst for the fabrication of direct formic acid fuel cells (DFAFC)
  • a cost-effective electrocatalyst for the oxidation of methanol
  • in the catalytic hydrogenation of chemical hydrides for the production of hydrogen
  • a catalyst in Suzuki-Mayaura reaction
Product can be used with our benchtop hydrogen generator, H-Genie Lite (Z744083)

Storage Class Code

11 - 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

Regulatory Listings

Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.

FSL

Group 2: Flammable solids
Metal powder
Hazardous rank II
1st combustible solid

JAN Code

205680-10G:
205680-BULK:
205680-VAR:
205680-100G:
205680-50G:

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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Soosan Kim et al.
Journal of hazardous materials, 392, 122464-122464 (2020-03-21)
The accumulation of industrial plastic waste in the environment is a global growing concern. Thermochemical process is a preferred method to dispose plastic waste mainly because it can reduce volume of the waste; however, the thermochemical disposal of plastic waste
Pd/C: an old catalyst for new applications-its use for the Suzuki-Miyaura reaction
Felpin F, et al.
European Journal of Organic Chemistry, 2006(12), 2679-2690 (2006)
Pd-C powder and thin film catalysts for hydrogen production by hydrolysis of sodium borohydride
Patel N, et al.
International Journal of Hydrogen Energy, 33(1), 287-292 (2008)
Heterogeneous Heck reaction catalyzed by Pd/C in ionic liquid
Hagiwara H, et al.
Tetrahedron Letters, 42(26), 4349-4351 (2001)
Svilen P Simeonov et al.
ChemSusChem, 12(12), 2748-2754 (2019-05-06)
A new scalable synthesis of pentane-1,2,5-triol from the furanics platform has been developed. Excellent yields of up to 92 % are obtained under flow conditions by using readily available catalysts from the existing pool. The strategy exploits the highly functionalized Achmatowicz
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