NaOTf

Sodium trifluoromethanesulfonate (NaOTf) is commonly known as trifluoromethanesulfonic acid or TFMS. Possessing unique properties, TFMS is water-soluble, anionic, and boasts a range of valuable attributes. As a colorless, odorless, and non-toxic substance, TFMS finds widespread use as a reagent in organic synthesis, a catalyst in industrial applications, and a buffer in various biochemical experiments. In scientific research, TFMS stands out due to its robust acidity, enabling it to act as a potent catalyst in organic synthesis. Additionally, it effectively serves as a reliable buffer at pH levels, ensuring precise pH maintenance in biochemical experiments. As an anionic compound, TFMS functions as a strong acid in solution, facilitating the donation of protons to other molecules, thus reducing the pH.

White to off-white powder

Sodium trifluoromethanesulfonate can be employed as a reagent for the preparation of:

• Aryl fluorides via silver-catalyzed fluorination of arylstannanes.
• Ionic liquids such as N, N -dialkylpyrrolidinium triflate, N,N-dialkylimidazolium triflate, and N-alkylpyridinium triflate.

It can be also used as supporting electrolyte in electrochemical O-glycosylation of primary alcohols with O-protected thioglycosides.

NaOTf is used in the preparation of N-fluoro-2-methylpyridinium triflate by reaction with dinitrogen difluoride as a reagent. It is also used as a chaotropic mobile phase additive in reversed-phase liquid chromatography (RP-LC).

NaOTf is prepared by adding a slight excess of sodium sulfate to an aqueous solution of barium trifluoromethanesulfonate. The reaction mixture is stirred for several minutes and allowed to stand for one day, and the white precipitate of barium sulfate is removed by filtration. The clear filtrate is evaporated to dryness, and the solid product is recrystallized from dry acetone. The salt is dried under vacuum at 110°C.1 Barium trifluoromethanesulfonate can be easily prepared from aqueous trifluoromethanesulfonic acid and barium carbonate. Other methods include the preparation of sodium trifluoromethane sulfonate from sodium dithionite and bromotrifluoromethane and its oxidation to sodium trifluoromethane sulfonate using hydrogen peroxide.

Sodium trifluoromethanesulfonate (Sodium triflate or NaOTf) is an efficient catalyst as well as a reagent in many organic reactions. The prominent application includes catalytic asymmetric Mannich-type reactions, Mannich-type reactions in water, and Diels-Alder reactions.

Hard carbon-based sodium-ion batteries (HC-based SIBs)  have poor performance at low temperatures. Jidao Li and colleagues^[1] propose an anion-inverted coordination electrolyte strategy using sodium trifluoromethanesulfonate (NaOTf). This optimized electrolyte enhances ionic conductivity, interfacial stability, and low-temperature performance.

soluble in water, alcohol, acetonitrile, N,N-dimethylformamide, and most highly polar organic solvents.

[1] Li, J., Long, J., Gong, H., Zhou, S., Wang, J., Jiang, Z., Huang, S., Zhou, Q., Wang, F., Shi, J., Zhang, Y., Bai, Z., & Tang, Y. (2026). Anion-inverted coordination: An "ice-breaking" ether electrolytes for low temperature sodium battery. Chemical Engineering Journal, 538, 176555. https://doi.org/10.1016/j.cej.2026.176555