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Atomfair Tetrabutylammonium Fluoride TBAF C16H36FN

Description Tetrabutylammonium Fluoride (TBAF) is a quaternary ammonium salt with the molecular formula C16H36FN. This highly versatile reagent is widely used in organic synthesis, particularly as a fluoride ion source for desilylation reactions. Available in anhydrous and trihydrate forms, our high-purity TBAF is rigorously tested to ensure consistent performance in sensitive applications. The compound is supplied as a white crystalline solid or as a solution in THF, with careful packaging to maintain stability. CAS 22206-57-1 (anhydrous) and 429-41-4 (trihydrate) variants are both available to meet your specific research needs. Key Features: Purity: ??98% (HPLC) Alternative CAS: 429-41-4 (trihydrate) Storage: Under…

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Description

Description

Tetrabutylammonium Fluoride (TBAF) is a quaternary ammonium salt with the molecular formula C16H36FN. This highly versatile reagent is widely used in organic synthesis, particularly as a fluoride ion source for desilylation reactions. Available in anhydrous and trihydrate forms, our high-purity TBAF is rigorously tested to ensure consistent performance in sensitive applications. The compound is supplied as a white crystalline solid or as a solution in THF, with careful packaging to maintain stability. CAS 22206-57-1 (anhydrous) and 429-41-4 (trihydrate) variants are both available to meet your specific research needs.

Key Features:

  • Purity: ??98% (HPLC)
  • Alternative CAS: 429-41-4 (trihydrate)
  • Storage: Under inert atmosphere at 2-8??C
  • Packaging: Glass bottles with secure seals
  • Hazard Class: 8 (Corrosive)
  • CAS No: 22206-57-1
  • Molecular Formula: C16H36FN
  • Molecular Weight: 261.46
  • Exact Mass: 261.28317831
  • Monoisotopic Mass: 261.28317831
  • IUPAC Name: tetrabutylazanium;fluoride
  • SMILES: CCCC[N+](CCCC)(CCCC)CCCC.[F-]
  • Synonyms: Tetrabutylammonium fluoride, 429-41-4, TETRA-N-BUTYLAMMONIUM FLUORIDE, UNII-2618F0C37I, EINECS 207-057-2

Application

Tetrabutylammonium Fluoride is primarily employed as a desilylating agent in organic synthesis, efficiently cleaving silicon-protecting groups from alcohols, phenols, and carboxylic acids. It serves as a strong base in elimination reactions and finds application in the preparation of fluoroorganic compounds. Researchers also utilize TBAF in material science for surface modification and as a phase-transfer catalyst in nucleophilic fluorination reactions.

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