Transition Metal Catalysts

Usually used as a catalyst for arylation reactions.

Palladium hydroxide.

Palladium hydroxide.

Palladium hydroxide.

DescriptionWe 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 catalysis.Click herefor more information.Hydrogenation

DescriptionWe 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 catalysis.Click herefor more information.Hydrogenation

Addition of Pd/C to Pd(OH)2/C improves the efficiency of N- or O-debenzylation.[2] Effectively catalyzes the direct arylation reactions of aryl iodides and bromides in both intra- and intermolecular processes. Particularly active for hydrogenolysis

Addition of Pd/C to Pd(OH)2/C improves the efficiency of N- or O-debenzylation.[2] Effectively catalyzes the direct arylation reactions of aryl iodides and bromides in both intra- and intermolecular processes. Particularly active for hydrogenolysis

Addition of Pd/C to Pd(OH)2/C improves the efficiency of N- or O-debenzylation.[2] Effectively catalyzes the direct arylation reactions of aryl iodides and bromides in both intra- and intermolecular processes. Particularly active for hydrogenolysis

Addition of Pd/C to Pd(OH)2/C improves the efficiency of N- or O-debenzylation.[2] Effectively catalyzes the direct arylation reactions of aryl iodides and bromides in both intra- and intermolecular processes. Particularly active for hydrogenolysis

DescriptionA robust palladium heterogenous catalyst.Catalyst for:Solvent-free hydrogenationAerobic alcohol oxidationA recyclable nanocatalyst for the racemization of primary amines. When used in conjunction with a lipase produces enantiopure amines

Palladium nitrate dihydrate.