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Tetrabutylammonium tetrafluoroborate
[CAS# 429-42-5]

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Complete supplier list of Tetrabutylammonium tetrafluoroborate
Identification
Classification Chemical reagent >> Organic reagent >> Amine salt (ammonium salt)
Name Tetrabutylammonium tetrafluoroborate
Molecular Structure CAS # 429-42-5, Tetrabutylammonium tetrafluoroborate
Molecular Formula C16H36N.BF4
Molecular Weight 329.27
CAS Registry Number 429-42-5
EC Number 207-058-8
SMILES [B-](F)(F)(F)F.CCCC[N+](CCCC)(CCCC)CCCC
Properties
Melting point 156-163 ºC
Water solubility Slightly soluble
Safety Data
Hazard Symbols symbol symbol   GHS05;GHS07 Danger    Details
Hazard Statements H302-H315-H318-H319-H335    Details
Precautionary Statements P261-P264-P264+P265-P270-P271-P280-P301+P317-P302+P352-P304+P340-P305+P351+P338-P305+P354+P338-P317-P319-P321-P330-P332+P317-P337+P317-P362+P364-P403+P233-P405-P501    Details
Hazard Classification
up    Details
HazardClassCategory CodeHazard Statement
Skin irritationSkin Irrit.2H315
Specific target organ toxicity - single exposureSTOT SE3H335
Eye irritationEye Irrit.2H319
Acute toxicityAcute Tox.4H302
Serious eye damageEye Dam.1H318
Acute toxicityAcute Tox.3H331
Chronic hazardous to the aquatic environmentAquatic Chronic1H410
Acute toxicityAcute Tox.3H311
Skin corrosionSkin Corr.1CH314
Acute toxicityAcute Tox.3H301
Skin corrosionSkin Corr.1BH314
SDS Available
up Discovory and Applicatios
Tetrabutylammonium tetrafluoroborate is an ionic liquid that has gained recognition for its unique properties and wide range of applications in chemical and industrial processes. This compound belongs to a class of ionic liquids known for their low volatility and high stability.

Tetrabutylammonium tetrafluoroborate (often abbreviated as [N4444][BF4]) was first synthesized in the mid-20th century as part of research to develop ionic liquids with desirable chemicophysical properties. The synthesis involves the reaction of tetrabutylammonium hydroxide with tetrafluoroboric acid, which produces a stable ionic liquid with tetrafluoroborate anions, which gives the compound its unique properties.

Tetrabutylammonium tetrafluoroborate is often used as an electrolyte in energy storage systems such as batteries and supercapacitors. Its high ionic conductivity and chemical stability make it an excellent choice to improve the performance and lifetime of these devices.

In organic synthesis, [N4444][BF4] is a versatile solvent. It is able to dissolve a wide range of organic and inorganic substances, thereby facilitating a variety of chemical reactions. This property is particularly useful in catalysis and extraction processes.

The compound is used in separation and extraction techniques in analytical chemistry. It helps to separate and purify target substances from complex mixtures, improving the accuracy and efficiency of analytical procedures.

Tetrabutylammonium tetrafluoroborate is used in the synthesis of advanced materials. Its role as a solvent or medium helps to form nanomaterials and other functional materials with specific properties. This application is important for the development of new materials with customized properties.

As a green solvent, [N4444][BF4] supports environmentally friendly chemical processes. Its low vapor pressure and reusability help reduce the environmental impact of industrial and research activities in line with sustainable practices.

Tetrabutylammonium tetrafluoroborate is known for its high stability and low volatility. These properties make it a safer and more reliable alternative to traditional solvents, minimizing the risks associated with volatile organic compounds. The ability of ionic liquids to dissolve a wide range of substances increases their usefulness in a variety of chemical processes. This versatility enhances its use in organic synthesis, separations, and materials science. The low toxicity and reusability of this compound make it a green choice for industrial and research applications. Its use helps reduce the environmental impact of chemical processes.

References

2010 Highly efficient macrolactonization of ?-hydroxy acids using benzotriazole esters: synthesis of Sansalvamide A. Organic & Biomolecular Chemistry, 8, 4940. DOI: 10.1039/c0ob00161a

2009 A new class of non-conjugated bipolar hybrid hosts for phosphorescent organic light-emitting diodes. Journal of Materials Chemistry, 19, 8772.
DOI: 10.1039/b909787b

2009 Electrochemical reduction of oxygen on nanoparticulate gold electrodeposited on a molecular template. Physical Chemistry Chemical Physics, 11, 3463. DOI: 10.1039/b818439a
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