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Grade
technical grade
Product Description
Application
Used as an etchant for silica films Reactant for: Nucleophilic fluorination Ring-opening fluorination reaction Substitution reactions Tetrabutylammonium hydrogen difluoride (TBABF) can be used as a reagent: For the conversion of aromatic boronic acids and esters into corresponding tetrabutylammonium trifluoroborate salts. These salts are utilized as surrogates of boronic acids in Suzuki-Miyaura cross-coupling reactions. In the nucleophilic fluorination of organic halides, tosylates, and triflates. For the regioselective synthesis of fluorohydrins by ring-opening of terminal epoxides.
Tetraalkylammonium salt - Hydrocarbon derivative - Organic salt - Amine - Organic cation - Aliphatic acyclic compound
Description
This compound belongs to the class of organic compounds known as tetraalkylammonium salts. These are organonitrogen compounds containing a quaternary ammonium substituted with four alkyl chains.
External Descriptors
Not available
1. Djoumbou Feunang Y, Eisner R, Knox C, Chepelev L, Hastings J, Owen G, Fahy E, Steinbeck C, Subramanian S, Bolton E, Greiner R, and Wishart DS. ClassyFire: Automated Chemical Classification With A Comprehensive, Computable Taxonomy. Journal of Cheminformatics, 2016, 8:61.
