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Tetraethylammonium fluoride hydrate, 97%
CAS: 98330-04-2 | C8H20FN | 149.25 g/mol
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Catalog number B23173.06
also known as B23173-06
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Quantity:
5 g
Price (USD)
80.65
Online Exclusive
89.40Save 8.75 (10%)
Each
Chemical Identifiers
CAS98330-04-2
IUPAC Nametetraethylazanium fluoride
Molecular FormulaC8H20FN
InChI KeyQSUJAUYJBJRLKV-UHFFFAOYSA-M
SMILES[F-].CC[N+](CC)(CC)CC
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Specifications
Specification Sheet
Specification SheetCommentSpecification differs for U.S. and non-U.S. material where indicated
Water Content (Karl Fischer Titration)≤30% (non-U.S. specification)
Assay from Suppliers CofA≥96.0% (U.S. specification)
Appearance (Color)White to pale cream
FormPowder or crystals or crystalline powder or lumpy crystalline powder
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Tetraethylammonium fluoride hydrate is used as a catalyst for oxidation, methylation and deuteration reactions of fluorine. It is involved as a reagent for the cleavage of Si-C bonds and also acts as a phase transfer catalyst in synthetic chemistry.
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
Tetraethylammonium fluoride hydrate is used as a catalyst for oxidation, methylation and deuteration reactions of fluorine. It is involved as a reagent for the cleavage of Si-C bonds and also acts as a phase transfer catalyst in synthetic chemistry.
Solubility
Soluble in water.
Notes
Hygroscopic. Air sensitive. Incompatible with strong oxidizing agents and strong bases.
Tetraethylammonium fluoride hydrate is used as a catalyst for oxidation, methylation and deuteration reactions of fluorine. It is involved as a reagent for the cleavage of Si-C bonds and also acts as a phase transfer catalyst in synthetic chemistry.
Solubility
Soluble in water.
Notes
Hygroscopic. Air sensitive. Incompatible with strong oxidizing agents and strong bases.
RUO – Research Use Only
General References:
- Otake, K.; Azukizawa, S.; Takeda, S.; Fukui, M.; Kawahara, A.; Kitao, T.; Shirahase, H. Novel 2,7-Substituted (S)-1,2,3,4-Tetrahydroisoquinoline-3-carboxylic Acids: Peroxisome Proliferator-Activated Receptor gamma Partial Agonists with Protein-Tyrosine Phosphatase 1B Inhibition. Chem. Pharm. Bull. 2015, 63 (12), 998-1014.
- Zheng, X.; Gandour, R. D.; Edgar, K. J. Probing the Mechanism of TBAF-Catalyzed Deacylation of Cellulose Esters. Biomacromolecules 2013, 14 (5), 1388-1394.