Certain features of will be down for maintenance Saturday afternoon/evening, February 24th starting at 3:00 pm CT until 9:00 pm CT.

Please note that you still have telephone and email access to our local offices. We apologize for any inconvenience.


Organoborates are convenient nucleophilic reagents due to their stability towards air and moisture; however, the stability does not hamper their high reactivity in a large variety of reactions, such as oxidative cross-coupling between the alkynyl and aryl ligands of the borates, forming an sp-sp2 carbon-carbon bond. Organoborates are involved in the sequence hydroboration-oxidation and are being investigated as electrolytes for lithium batteries.

Product #



Molecular Formula

Add to Cart

92330 Trimethyl borate purum, ≥99.0% (GC) C3H9BO3
447218 Trimethyl borate 99.999% (trace metal basis) C3H9BO3
443999 Trimethyl borate purified by redistillation, ≥99.5% C3H9BO3
452920 Trimethyl borate ≥98% C3H9BO3
790877 Tris(2,2,2-trifluoroethyl) borate 97% C6H6BF9O3
T59307 Triethyl borate 99% C6H15BO3
673943 2-Methoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 96% C7H15BO3
417149 2-Isopropoxy-4,4,5,5-tetramethyl-1,3,2-dioxaborolane 98% C9H19BO3
197335 Triisopropyl borate ≥98% C9H21BO3
348635 Tris(trimethylsilyl) borate 99% C9H27BO3Si3
236608 Tri-tert-butyl borate 98% C12H27BO3
90795 Tributyl borate ≥99.0% (T) C12H27BO3
418714 Triphenyl borate ≥97% C18H15BO3
CDS000471 Trihexadecyl borate AldrichCPR C48H99BO3