Tetra-n-butylammonium fluoride, 75% w/w aq. soln.
Tetra-n-butylammonium fluoride, 75% w/w aq. soln.
Tetra-n-butylammonium fluoride, 75% w/w aq. soln.
Thermo Scientific Chemicals

Tetra-n-butylammonium fluoride, 75% w/w aq. soln.

CAS: 429-41-4 | C16H36FN | 261.47 g/mol
Have Questions?
變更視圖buttonViewtableView
Quantity:
25 g
100 g
500 g
產品號碼 B21261.36
亦稱為 B21261-36
價格 (TWD)
-
Quantity:
500 g
Request bulk or custom format
化學識別
CAS429-41-4
IUPAC Nametetrabutylazanium fluoride
Molecular FormulaC16H36FN
InChI KeyFPGGTKZVZWFYPV-UHFFFAOYSA-M
SMILES[F-].CCCC[N+](CCCC)(CCCC)CCCC
檢視更多
規格Specification Sheet規格表
Appearance (Color)Clear colorless to yellow
FormViscous liquid
Assay (Non-aqueous acid-base Titration)≥70.0 to ≤80.0%
Water Content (Karl Fischer Titration)≥20.0 to ≤30.0%
Tetrabutylammonium Fluoride is a reactant used for the synthesis of multiple compounds, including conjugated dienoic acid esters, oligoribonucleotides with phosphonate-modified linkages, and triple monoamine reuptake inhibitors, among others. It has proven useful in studying cancer, diabetes, and neurochemistry.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Tetrabutylammonium Fluoride is a reactant used for the synthesis of multiple compounds, including conjugated dienoic acid esters, oligoribonucleotides with phosphonate-modified linkages, and triple monoamine reuptake inhibitors, among others. It has proven useful in studying cancer, diabetes, and neurochemistry.

Solubility
Insoluble in water.

Notes
Hygroscopic. Store in cool place. Keep container tightly closed in a dry and well-ventilated place. Stable under recommended storage conditions.Keep away from strong oxidizing agents,
RUO – Research Use Only

General References:

  1. GVM Sharma.; VG Reddy.; AS Chander. Tetra-n-butylammonium fluoride: an efficient base for aza-Michael addition—synthesis of glycosyl β-amino acid esters. Tetrahedron: Asymmetry. 200213 (1), 21-24.
  2. AH Narten.; S Lindenbaum. Diffraction Pattern and Structure of the System Tetra-n-butylammonium Fluoride-Water at 25°C. The Journal of Chemical Physics. 196951 (1), 1108-1110.