Organoaluminum [Organometallic Reagents] — this collection brings together organoaluminum compounds, namely aluminum complexes bonded to alkoxide, alkyl, or beta-diketonate ligands, which function as Lewis acids and catalysts in various organic reactions. Aluminum–oxygen or aluminum–carbon bonds provide distinctive reactivity that is utilized to activate carbonyl groups as well as accelerate polymerization reactions.
Organoaluminum compounds in this category are used as catalysts or auxiliary reagents in Meerwein-Ponndorf-Verley and Oppenauer reactions, olefin polymerization, and various addition and coordination reactions that require carbonyl activation by a Lewis acid. Synthetic organic chemists and polymer materials researchers use these alkoxide and alkyl aluminum derivatives to control selectivity and reaction rate in laboratory-scale synthesis.
Example products in this collection: TCI A0244 2269-22-9 Aluminum sec-Butoxide, TCI M1211 56252-55-2 Methylaluminum Bis(2,6-di-tert-butyl-4-methylphenoxide) (0.4mol/L in Toluene), TCI A0241 13963-57-0 Tris(2,4-pentanedionato)aluminum(III), TCI A0245-250G 555-75-9 Aluminum Ethoxide, TCI A1267 14354-59-7 Tris(trifluoro-2,4-pentanedionato)aluminum(III), TCI A0804 556-91-2 Aluminum tert-Butoxide.
Selecting an organoaluminum compound requires attention to the type of ligand (alkoxide, alkyl, or beta-diketonate), the concentration where provided as a solution in solvent, and its sensitivity to atmospheric moisture, which calls for special handling and packaging. All products are genuine products of Tokyo Chemical Industry (TCI) Japan, with purity, packaging, and storage conditions listed on each item's page.
Other parallel categories under Organometallic Reagents, often used together in one laboratory workflow:
Back to Organometallic Reagents. For large-volume procurement, special packaging, or specific grades, contact the AMI Scientific team — official distributor of TCI Japan in Indonesia — to check availability and lead time directly from Japan.
