Collection: Palladium Catalysts [Cross-coupling Reaction using Transition Metal Catalysts]

Palladium Catalysts [Cross-coupling Reaction using Transition Metal Catalysts] — includes palladium(0) and palladium(II) complexes with various phosphine ligands, N-heterocyclic carbenes (NHC), and acetonitrile, ranging from classic complexes to newer precatalysts that are more stable toward air. These complexes serve as the core catalysts in transition-metal-mediated carbon-carbon bond-forming cycles.

Palladium Catalysts are used by synthetic organic and pharmaceutical chemists for cross-coupling reactions such as Suzuki, Negishi, Sonogashira, Heck, and Buchwald-Hartwig in the formation of carbon-carbon as well as carbon-nitrogen bonds. Bulky phosphine ligands and NHC complexes are chosen for aryl chlorides that are less reactive or for reactions at low temperature, while Pd(0) precatalysts are used directly without an additional activation step. These catalysts form the backbone of complex molecule synthesis in research laboratories and at process scale.

Product examples in this collection: TCI T3023 68569-14-2 Tetrakis(acetonitrile)palladium(II) Bis(trifluoromethanesulfonate), TCI B6199 905459-27-0 [1,3-Bis(2,6-Diisopropylphenyl)imidazol-2-ylidene](3-chloropyridyl)palladium(II) Dichloride, TCI T2184 51364-51-3 Tris(dibenzylideneacetone)dipalladium(0), TCI B6255 887919-35-9 Bis[di-tert-butyl(4-dimethylaminophenyl)phosphine]dichloropalladium(II), TCI T1350 14221-01-3 Tetrakis(triphenylphosphine)palladium(0), TCI B7081 1071965-73-5 Bromo[4-(trifluoromethyl)phenyl][tris(1,1-dimethylethyl)phosphine]palladium, TCI B3224 31277-98-2 Bis[1,2-bis(diphenylphosphino)ethane]palladium(0), TCI C2372 930796-10-4 Chloro[[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](N,N-dimethylbenzylamine)palladium(II)].

Choose based on the oxidation state of palladium, the type of ligand such as bulky phosphine, NHC, or bidentate, and stability toward air and moisture, according to the type of coupling reaction and the aryl substrate used. All products are genuine Tokyo Chemical Industry (TCI) Japan products, with purity, packaging, and storage conditions listed on the page of each item.

Other parallel categories under Cross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation], often used together in one laboratory workflow:

• Phosphine Ligands [Cross-coupling Reaction using Transition Metal Catalysts]
• N-Heterocyclic Carbene (NHC) Ligands [Cross-coupling Reaction using Transition Metal Catalysts]
• Nickel [Catalysis and Inorganic Chemistry]
• Nickel Catalysts [Cross-coupling Reaction using Transition Metal Catalysts]
• Copper Catalysts [Cross-coupling Reaction using Transition Metal Catalysts]
• Bases and Additives [Cross-coupling Reaction using Transition Metal Catalysts]

Back to Cross-coupling Reaction using Transition Metal Catalysts [C-C Bond Formation]. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — the official TCI Japan distributor in Indonesia — to check availability and lead time directly from Japan.