Tetrabutylammonium fluoride
[CAS# 429-41-4]

Identification

• Classification: Surfactant >> Cationic surfactant >> Quaternary ammonium salt type
• Name: Tetrabutylammonium fluoride
• Synonyms: TBAF
• Molecular Formula: C₁₆H₃₆FN
• Molecular Weight: 261.46
• CAS Registry Number: 429-41-4
• EC Number: 207-057-2
• SMILES: CCCC[N+](CCCC)(CCCC)CCCC.[F-]

Properties

• Density: 0.903 g/mL (Expl.)
• Melting point: 54-60 ºC (Expl.)
• Flash point: -17 ºC (Expl.)

Safety Data

• Hazard Symbols: GHS05;GHS07 Danger
• Hazard Statements: H314-H318-H335
• Precautionary Statements: P260-P261-P264-P264+P265-P271-P273-P280-P301+P330+P331-P302+P361+P354-P304+P340-P305+P354+P338-P316-P317-P319-P321-P363-P403+P233-P405-P501

Hazard Classification

Hazard	Class	Category Code	Hazard Statement
Skin corrosion	Skin Corr.	1B	H314
Specific target organ toxicity - single exposure	STOT SE	3	H335
Serious eye damage	Eye Dam.	1	H318
Skin corrosion	Skin Corr.	1C	H314
Acute toxicity	Acute Tox.	3	H301
Acute toxicity	Acute Tox.	4	H302
Flammable liquids	Flam. Liq.	2	H225
Carcinogenicity	Carc.	2	H351
Acute toxicity	Acute Tox.	3	H311
Acute toxicity	Acute Tox.	4	H312
Acute toxicity	Acute Tox.	4	H332
Specific target organ toxicity - repeated exposure	STOT RE	1	H372

• Transport Information: UN 3261

Discovory and Applicatios

Tetrabutylammonium fluoride (TBAF) is a quaternary ammonium salt with the chemical formula (C4H9)4NF. It consists of a tetrabutylammonium cation (C4H9)4N+ paired with a fluoride anion (F−). This compound is typically encountered as a colorless, hygroscopic solid, or in solution. TBAF is known for its distinctive reactivity and has important applications in both synthetic chemistry and material science.

The discovery and development of tetrabutylammonium fluoride occurred alongside the exploration of various quaternary ammonium salts, which are widely used as catalysts, reagents, and phase transfer agents in chemical processes. These salts, including TBAF, are recognized for their ability to dissolve in both polar and nonpolar solvents, as well as their utility in facilitating reactions that involve the transfer of ions or molecules between different phases. The fluoride anion in TBAF is particularly reactive, making this compound useful in several chemical processes, particularly those that involve fluorine chemistry.

Tetrabutylammonium fluoride has several applications in organic synthesis. One of its most important uses is as a fluoride source in reactions that require the introduction of a fluoride ion into an organic molecule. The fluoride anion is highly nucleophilic and can participate in various substitution reactions, including the deprotection of silyl ethers in organic synthesis. In these reactions, TBAF is often used to remove protective groups such as silyl groups (e.g., trimethylsilyl or tert-butyldimethylsilyl groups) from oxygen atoms in alcohols, phenols, and other functional groups, which is a critical step in many synthetic pathways. This ability to remove silyl groups efficiently is valuable in the synthesis of complex organic compounds, including pharmaceuticals and natural products.

In addition to its role in silylation and deprotection reactions, TBAF is also used in the preparation of organofluorine compounds. The fluoride anion from TBAF can replace other halides or leaving groups in various substitution reactions to introduce fluorine into organic molecules. Fluorinated compounds are of significant interest in various fields, including medicinal chemistry, agrochemicals, and materials science, as fluorine can modify the physical and chemical properties of a molecule in ways that enhance its stability, bioactivity, or electronic properties.

TBAF is also used in polymer chemistry. It is sometimes employed in the preparation of polymer-bound fluorine compounds, which can be utilized in the development of new materials, including ion-conducting polymers and membranes for energy storage and conversion devices. The fluoride ion is involved in ionic conductivity and other properties that are crucial for the performance of materials in electrochemical applications.

Another application of tetrabutylammonium fluoride is in the field of phase transfer catalysis. In these reactions, TBAF can facilitate the transfer of fluoride ions between immiscible phases, typically from an aqueous phase to an organic phase. This ability is particularly useful in reactions that require a fluoride source but where the reagents or products are not soluble in the same solvent. TBAF’s role in phase transfer catalysis helps increase the efficiency and yield of reactions by ensuring that the fluoride anion is available in the appropriate phase.

Despite its usefulness, TBAF must be handled with care. The fluoride ion is toxic and can cause significant damage to tissues upon contact. Therefore, when working with TBAF, appropriate safety precautions, including the use of gloves, protective eyewear, and fume hoods, should be taken. Additionally, TBAF is hygroscopic, meaning that it readily absorbs water from the atmosphere, which can lead to the formation of hydrofluoric acid (HF), a highly corrosive substance. Therefore, TBAF should be stored in a dry environment to maintain its stability.

In summary, tetrabutylammonium fluoride is a versatile chemical compound with important applications in organic synthesis, fluorine chemistry, polymer chemistry, and phase transfer catalysis. Its ability to provide a reactive fluoride ion makes it a valuable reagent in various chemical processes, particularly those that require selective deprotection or the introduction of fluorine into organic molecules. The continued use and study of TBAF highlight its significant role in modern synthetic chemistry and materials science.

References

2025 Design, Synthesis, and Cellular Imaging Application of a Fluorescent Probe Based on Fluoride Ion-Induced Cyclization of Phenothiazine Derivatives. Journal of Fluorescence, 2025, 1.
DOI: 10.1007/s10895-023-03526-3

2024 Ring opening of epoxides: a facile approach towards the synthesis of polyketides and related stereoenriched natural products: a review. Molecular Diversity, 2024, 1.
DOI: 10.1007/s11030-024-11057-7

2024 Asymmetric dearomative single-atom skeletal editing of indoles and pyrroles. Nature Chemistry, 2024, 1.
DOI: 10.1038/s41557-024-01680-0