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Triisopropyl borate is used as reagent in Pd-catalyzed coupling reaction with aryl halides such as Suzuki reaction. It is used as a reagent for the preparation of the boronic acids and esters; as a Lewis acid catalyst and involved in the ortho-borylation of 1-substituted naphthalenes. Furthermore, it plays an important role as a catalyst for the production of resins, waxes, paints and varnishes.
Reagent for preparation of boronates from Grignard or organolithium reagents, often giving higher yields than other trialkyl borates: Organometallics, 2, 1316 (1983); Tetrahedron Lett ., 29, 2631 (1988).
Garcia-Alonso, D.; Potts, S. E.; van Helvoirt, C. A.; Verheijen, M. A.; Kessels, W. M. Atomic layer deposition of B-doped ZnO using triisopropyl borate as the boron precursor and comparison with Al-doped ZnO. J. Mater. Chem. C 2015, 3 (13), 3095-3107.
Lyu, S. C.; Han, J. H.; Shin, K. W.; Sok, J. H. Synthesis of boron-doped double-walled carbon nanotubes by the catalytic decomposition of tetrahydrofuran and triisopropyl borate. Carbon 2011, 49 (5), 1532-1541.
Hazard Statements: H225
Highly flammable liquid and vapour.
Precautionary Statements: P210-P280a-P240-P241-P303+P361+P353-P501a
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. IF ON SKIN (or hair): Remove/Take off immediately all contaminated clothing. Rinse skin with water/shower. Dispose of contents/container in accordance with local/regional/national/international regulations.