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674133

Sigma-Aldrich

Palladium nanoparticles entrapped in aluminum hydroxide matrix

0.5 wt. % loading

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About This Item

Linear Formula:
Pd/AlO(OH)
UNSPSC Code:
12161600
PubChem Substance ID:
24885199
NACRES:
NA.22

form

solid

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

SMILES string

[Pd].O[Al]=O

InChI

1S/Al.H2O.O.Pd/h;1H2;;/q+1;;;/p-1

InChI key

BBEPUHUDSUQPRM-UHFFFAOYSA-M

General description

A robust palladium heterogenous catalyst.

Application

Catalyst for:
  • Solvent-free hydrogenation
  • Aerobic alcohol oxidation
A recyclable nanocatalyst for the racemization of primary amines. When used in conjunction with a lipase produces enantiopure amines by Dynamic Kinetic Resolution.

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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.

JAN Code

674133-10G:
674133-VAR:
674133-BULK:

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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Min Serk Kwon et al.
Organic letters, 7(6), 1077-1079 (2005-03-12)
[reaction: see text] A new aluminum hydroxide-supported palladium catalyst (1) made by a one-pot synthesis through nanoparticle generation and gelation shows a dual catalytic activity for olefinic hydrogenation and aerobic alcohol oxidation.
Mahn-Joo Kim et al.
Organic letters, 9(6), 1157-1159 (2007-02-13)
A practical procedure for the dynamic kinetic resolution (DKR) of primary amines has been developed. This procedure employs a palladium nanocatalyst as the racemization catalyst, a commercial lipase (Novozym-435) as the resolution catalyst, and ethyl acetate or ethyl methoxyacetate as

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