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It is a catalyst used in Stille reaction, hydrogenation reactions, Suzuki-Miyaura cross-coupling and Heck-Mizoroki reactions, deoxygenation, oxidation reactions and coupling reactions.
Hydrogenation catalyst, which may be preferred where deactivation by the reaction products is possible:
Used in low-pressure hydrogenolysis of N-benzylamines: Org. Synth. Coll., 7, 152 (1990). Reduction of oximes to amines: Org. Synth. Coll., 5, 376 (1973). Widely used along with hydrogen donors such as Ammonium formate, A10699, Sodium formate, A17813, Formic acid, A13285, Cyclohexene, A11359, or Hydrazine monohydrate, A14005, for catalytic transfer hydrogenation reactions. In combination with Sodium borohydride, 13432, promotes the reduction of nitro-compounds to amines, where borohydride alone is ineffective: Synthesis, 713 (1987).
Dinh, L. N.; Cairns, G. A.; Strickland, R. A.; McLean, W.; Maxwell, R. S. Mechanism and Kinetic Modeling of Hydrogenation in the Organic Getter/Palladium Catalyst/Activated Carbon Systems. J. Phys. Chem. A. 2015, 119 (6), 943-951.
Liu, X.; Zhang, Z.; Yang, Y.; Yin, D.; Su, S.; Lei, D.; Yang, J. Selective hydrogenation of citral to 3,7-dimethyloctanal over activated carbon supported nano-palladium under atmospheric pressure. Chem. Eng. J. 2015, 263, 290-298.
Gefahrenhinweise (EU): H228
Keep away from heat/sparks/open flames/hot surfaces. - No smoking. Wear protective gloves and eye/face protection. Ground/bond container and receiving equipment. Use explosion-proof electrical/ventilating/lighting/ equipment. In case of fire: Use for extinction: CO2, powder or water spray.