SODIUM TRIFLUOROMETHANESULFONATE MARKET

INTRODUCTION

 A mild excess of sodium sulfate is added to an aqueous solution of barium trifluoromethanesulfonate to create Sodium Trifluoromethanesulfonate .

For the manufacture of alkali metal and silver trifluoromethanesulfonate, barium trifluoromethanesulfonate has been commonly employed since barium can be easily extracted as its insoluble sulfate.

The reaction mixture is agitated for a few minutes and left to stand for a day before the white barium sulfate precipitate is filtered out.

The solid product is recrystallized from dry acetone after the clear filtrate has been evaporated to dryness. At 110 °C, the salt is dried in a vacuum.

Aqueous trifluoromethanesulfonic acid and barium carbonate can be used to make barium trifluoromethanesulfonate quickly and efficiently.

The creation of sodium trifluoromethanesulfinate from sodium dithionite and bromotrifluoromethane are further techniques.

Sodium Trifluoromethanesulfonate acid has a pKa of 0.23, making it a very weak base when compared to acetic acid, which has a pKa of 4.76.

This is because the three fluorine atoms next to the carboxylate group have an electron-withdrawing effect. Trifluoroacetate ion can be protonated to Sodium Trifluoromethanesulfonate acid by strong acids like sulfuric or hydrochloric acid:CF 3 CO 2 + HCl becomes CF 3 CO 2 H + Cl in the display style "ce" formula.CF 3 CO 2 + H 2 SO 4 becomes CF 3 CO 2 H + HSO 4 using the displaystyle "ce" command.

In general, trifluoroacetate produces trifluoroacetic acid when it interacts in equilibrium with hydronium cations:CF 3 CO 2 + H 3 O + + CF3 CO2H + H2O.

SODIUM TRIFLUOROMETHANESULFONATE MARKET SIZE AND FORECAST

The Global Sodium Trifluoromethanesulfonate Market accounted for $XX Billion in 2022 and is anticipated to reach $XX Billion by 2030, registering a CAGR of XX% from 2024 to 2030.

SODIUM TRIFLUOROMETHANESULFONATE MARKETRECENT UPDATE

In many chemical processes, sodium trifluoromethanesulfonate (also known as sodium triflate or NaOTf) serves as both a reagent and an effective catalyst.

Catalytic asymmetric Mannich-type reactions, Mannich-type reactions in water, and Diels-Alder reactions are some of the main applications.

Application-As a reagent, sodium trifluoromethanesulfonate is useful in the production of:By fluorinated aryl stannanes under the influence of silver, aryl fluores.N,N-dialkyl pyrrolidinium triflate, N,N-dialkylimidazolium triflate, and N-alkylpyridinium triflate are examples of ionic liquids.

In electrochemical O-glycosylation of primary alcohols with O-protected thioglycosides, it can also be utilized as a supportive electrolyte.Packaging 5, 25 g in a bottle of glass.

SODIUM TRIFLUOROMETHANESULFONATE MARKETCOMPANY PROFILE

• Central Glass
• Solvay
• Time Chemical
• 718th Research Institute of CSIC
• Russia Aecc
• Oakwood Chemicals

SODIUM TRIFLUOROMETHANESULFONATE MARKETTHIS REPORT WILL ANSWER FOLLOWING QUESTIONS

1. How many Sodium Trifluoromethanesulfonate are manufactured per annum globally? Who are the sub-component suppliers in different regions?
2. Cost breakup of a Global Sodium Trifluoro methane sulfonate and key vendor selection criteria
3. Where is the Sodium Trifluoromethanesulfonate manufactured? What is the average margin per unit?
4. Market share of Global Sodium Trifluoromethanesulfonate market manufacturers and their upcoming products
5. Cost advantage for OEMs who manufacture Global Sodium Trifluoromethanesulfonate in-house
6. key predictions for next 5 years in Global Sodium Trifluoromethanesulfonate market
7. Average B-2-B Sodium Trifluoromethanesulfonate market price in all segments
8. Latest trends in Sodium Trifluoromethanesulfonate market, by every market segment
9. The market size (both volume and value) of the Sodium Trifluoromethanesulfonate market in 2024-2030 and every year in between?
10. Production breakup of Sodium Trifluoromethanesulfonate market, by suppliers and their OEM relationship