Trifluoromethanesulfonic acid CAS: 1493-13-6
Catalog Number | XD93573 |
Product Name | Trifluoromethanesulfonic acid |
CAS | 1493-13-6 |
Molecular Formula | CHF3O3S |
Molecular Weight | 150.08 |
Storage Details | Ambient |
Product Specification
Appearance | White powder |
Assay | 99% min |
Trifluoromethanesulfonic acid (CF3SO3H), commonly known as triflic acid, is a highly reactive and strong acid that finds extensive use in various chemical processes and industries. It is widely utilized as a catalyst, solvent, and reagent due to its exceptional acidity and unique properties.One of the primary applications of trifluoromethanesulfonic acid is as a superacid catalyst. It is considered one of the strongest Brønsted acids known, surpassing sulfuric, hydrochloric, and even fluorosulfuric acid in terms of acidity. This remarkable acidity allows triflic acid to catalyze various reactions that require strong acid conditions, including esterification, acylation, alkylations, and rearrangements. It is particularly valuable for promoting reactions that involve carbocations, as it stabilizes and enhances their reactivity.Triflic acid is also employed as a solvent for certain reactions, especially those that require highly acidic environments. It can dissolve a wide range of organic and inorganic compounds, making it useful for reactions that involve polar and nonpolar solutes. Additionally, its strong acidic nature can enhance solubility and aid in reaction kinetics.Another important use of trifluoromethanesulfonic acid is in the production of triflates. Triflic acid can react with alcohols, amines, and other nucleophiles to form their corresponding triflates (CF3SO3-), which are highly stable and versatile functional groups. Triflates can serve as good leaving groups or activate nucleophiles, enabling a variety of subsequent reactions such as nucleophilic substitutions, rearrangements, and carbon-carbon bond formations.Furthermore, triflic acid has applications in the synthesis of pharmaceuticals, agrochemicals, and specialty chemicals. Its unique reactivity and acidity make it a valuable reagent for the formation of complex organic molecules. Additionally, it can exhibit selective reactivity, enabling it to target specific functional groups or positions in a molecule, facilitating the synthesis of specific isomers or enantiomers.It is important to note that trifluoromethanesulfonic acid should be handled with extreme care due to its highly corrosive nature. Proper safety precautions, including the use of protective equipment and working under suitable ventilation, should be followed to minimize risks.In summary, trifluoromethanesulfonic acid is a powerful acid with various applications in chemical processes and industries. Its exceptionally strong acidity enables it to catalyze a wide range of reactions, act as a solvent, and participate in the formation of stable functional groups. Its versatility and reactivity make it an indispensable reagent for the synthesis of complex organic molecules. However, caution must be exercised when handling triflic acid, adhering to proper safety protocols to ensure the well-being of the chemist and prevent accidents.