Organotin [Organometallic Reagents] — covers organotin compounds with single or multiple carbon–tin bonds, including organic tin halides and oxides, which act as transition-metal reagents in carbon–carbon bond formation and transmetalation reactions in complex organic synthesis.
Organotin reagents are widely used in Stille coupling reactions to form carbon–carbon bonds in the synthesis of complex aromatic and heterocyclic molecules, including by synthetic organic chemistry researchers and for functional materials such as thiophene-based organic semiconductors. Their halide and oxide derivatives also serve as precursors in catalyst preparation and surface modification of materials.
Examples of products in this collection: TCI T3703 1112-56-7 Tetravinylstannane, TCI B5690 178931-63-0 5,5''-Bis(trimethylstannyl)-2,2':5',2''-terthiophene, TCI T2009 7393-43-3 Tetraallyltin, TCI B6395 86134-26-1 2,5-Bis(trimethylstannyl)thiophene, TCI T1928 59020-06-3 Trimethyl(4-pyridyl)tin, TCI D0223 683-18-1 Dibutyltin Dichloride, TCI T1742 13737-05-8 Trimethyl(2-pyridyl)tin, TCI D0302 1067-33-0 Dibutyltin Diacetate.
Choose according to the type of alkyl/aryl substituent and the degree of substitution on the tin atom, and pay attention to the compound's stability against air and moisture during storage and handling in the laboratory. All products are genuine Tokyo Chemical Industry (TCI) Japan products, with purity, packaging, and storage conditions listed on each item's page.
Other parallel categories under Organometallic Reagents, often used together in a single laboratory workflow:
This collection is further divided into 3 more specific groups:
Back to Organometallic Reagents. 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.
