Date published: 2025-11-12

1-800-457-3801

SCBT Portrait Logo
Seach Input

Trifluoromethanesulfonic acid (CAS 1493-13-6)

5.0(1)
Write a reviewAsk a question

Alternate Names:
Triflic acid; Perfluoromethanesulfonic acid; Trimsylate
Application:
Trifluoromethanesulfonic acid is a strong monoprotic acid
CAS Number:
1493-13-6
Purity:
≥98%
Molecular Weight:
150.08
Molecular Formula:
CF3SO3H
Supplemental Information:
This is classified as a Dangerous Good for transport and may be subject to additional shipping charges.
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

QUICK LINKS

Trifluoromethanesulfonic acid (TfOH) is a compound of significant interest in scientific research due to its unique properties and versatile applications across various disciplines. One of its primary mechanisms of action lies in its role as a strong acid catalyst. Trifluoromethanesulfonic acid′s high acidity, attributed to the electronegativity of the trifluoromethylsulfonyl group, makes it a potent catalyst for a wide range of organic transformations. In organic synthesis, TfOH facilitates reactions such as esterifications, acylations, and rearrangements by protonating reactants and activating functional groups. Moreover, TfOH finds extensive use in polymer chemistry for the polymerization of various monomers, including olefins, epoxides, and vinyl ethers. Its ability to initiate cationic polymerization reactions under mild conditions enables the synthesis of high molecular weight polymers with controlled architectures and properties. Additionally, research efforts have explored its potential in materials science, where it serves as a key component in the fabrication of organic-inorganic hybrid materials and functionalized surfaces. Furthermore, trifluoromethanesulfonic acid is utilized in analytical chemistry as a reagent for the determination and quantification of certain analytes. Its reaction with specific functional groups, such as alcohols and amines, enables their derivatization and subsequent analysis via chromatographic or spectroscopic techniques. Overall, trifluoromethanesulfonic acid continues to be a versatile and indispensable tool in scientific investigations, owing to its diverse functionalities and broad utility in research applications spanning organic synthesis, polymer chemistry, materials science, and analytical chemistry.


Trifluoromethanesulfonic acid (CAS 1493-13-6) References

  1. Trifluoromethanesulfonic Acid, an Unusually Powerful Catalyst for the Michael Addition Reaction of beta-Ketoesters under Solvent-Free Conditions.  |  Kotsuki, H., et al. 1999. J Org Chem. 64: 3770-3773. PMID: 11674516
  2. Trifluoromethanesulfonic acid-based proteomic analysis of cell wall and secreted proteins of the ascomycetous fungi Neurospora crassa and Candida albicans.  |  Maddi, A., et al. 2009. Fungal Genet Biol. 46: 768-81. PMID: 19555771
  3. Interaction of acetonitrile with trifluoromethanesulfonic acid: unexpected formation of a wide variety of structures.  |  Salnikov, GE., et al. 2012. Org Biomol Chem. 10: 2282-8. PMID: 22322594
  4. Effective Friedel-Crafts acylation of biotin acid chloride in trifluoromethanesulfonic acid.  |  Muto, Y., et al. 2012. Biosci Biotechnol Biochem. 76: 2162-4. PMID: 23132579
  5. Trifluoromethanesulfonic acid catalyzed friedel-Crafts alkylations of 1,2,4-trimethoxybenzene with aldehydes or benzylic alcohols.  |  Wilsdorf, M., et al. 2013. Org Lett. 15: 2494-7. PMID: 23642222
  6. Trifluoromethanesulfonic acid catalyzed synergetic oxidative/[3+2] cyclization of quinones with olefins.  |  Meng, L., et al. 2013. Angew Chem Int Ed Engl. 52: 10195-8. PMID: 23939998
  7. t-boc synthesis of huwentoxin-i through native chemical ligation incorporating a trifluoromethanesulfonic acid cleavage strategy.  |  Thapa, P., et al. 2016. Biopolymers. 106: 737-45. PMID: 27271997
  8. Exposure to low concentration of trifluoromethanesulfonic acid induces the disorders of liver lipid metabolism and gut microbiota in mice.  |  Zhou, J., et al. 2020. Chemosphere. 258: 127255. PMID: 32554004
  9. Trifluoromethanesulfonic Acid Promoted Controllable Electrophilic Aromatic Nitration.  |  Wu, Y., et al. 2023. J Org Chem. 88: 11322-11327. PMID: 37463455
  10. Deglycosylation with trifluoromethanesulfonic acid differentially affects inhibitor activities of turkey ovomucoid.  |  Dabich, D., et al. 1993. Biochim Biophys Acta. 1164: 47-53. PMID: 8390860

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Trifluoromethanesulfonic acid, 10 g

sc-203415
10 g
$33.00

Trifluoromethanesulfonic acid, 50 g

sc-203415A
50 g
$97.00

Trifluoromethanesulfonic acid, 100 g

sc-203415B
100 g
$163.00