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Sigma-Aldrich

Palladium on barium sulfate

greener alternative

extent of labeling: 5 wt. % loading, unreduced

Synonym(s):

Pd/BaSO4, Rosenmund catalyst

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About This Item

Linear Formula:
Pd
MDL number:
UNSPSC Code:
12141733
eCl@ss:
38191001
PubChem Substance ID:
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

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extent of labeling

5 wt. % loading

greener alternative category

SMILES string

[Pd]

InChI

1S/Pd

InChI key

KDLHZDBZIXYQEI-UHFFFAOYSA-N

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Application

Palladium on barium sulfate (Pd/BaSO4), also known as Rosenmund catalyst, is used for the decarboxylation of aliphatic esters for further production of biodiesel. It can also be used in hydrogenation reaction. Pd/BaSO4 may be used as a catalyst reservoir for the Stille cross-coupling reaction between iodobenzene and tributylphenyltin.

Other Notes

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.

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

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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Palladium on carbon-catalyzed solvent-free and solid-phase hydrogenation and Suzuki-Miyaura reaction
Monguchi Y, et al.
Tetrahedron, 67(45), 8628-8634 (2011)
Stille cross-coupling reaction using Pd/BaSO4 as catalyst reservoir
Coelho AV, et al.
Applied Organometallic Chemistry, 22(1), 39-42 (2008)
Palladium-catalyzed decarboxylation of higher aliphatic esters: Towards a new protocol to the second generation biodiesel production
Han J, et al.
Green Chemistry, 12(3), 463-467 (2010)

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