Triflic acid, >99%

Price range: $267.00 through $2,965.50

Product Code: KI-0008-HP

CAS NO: 1493-13-6

  • Chemical Formula: CHF3O3S
  • Synonyms: TfOH, as triflic acid, TFMS, TFSA, HOTf

**This product will incur a $97.00 HazMat fee when the order is placed**

Clear
Category:

SUM Formula: CHF3O3S

Molecular Weight: 150.08

Purity: >99%

  • SUM Formula: CHF3O3S
  • Molecular Weight: 150.08

Triflic acid, CAS: 1493-13-6

Key Applications:

1. Organic Synthesis & Reaction Activation

  • Protonates weakly basic substrates and hydrocarbons, enabling otherwise inaccessible transformations.
  • Facilitates Friedelโ€“Crafts alkylation and acylation, esterification, dehydration, and rearrangement reactions.
  • Used to generate highly reactive intermediates, including carbocations and sulfonate esters.
  • Serves as a strong acid catalyst in protecting group chemistry, including tertโ€‘butyl and silyl group manipulations.

2. Catalysis in Industrial & Fine Chemical Manufacturing

  • Acts as a robust, nonโ€‘oxidizing acid catalyst in pharmaceutical synthesis, improving yields and selectivity in key steps.
  • Supports polymerization reactions, including cationic polymerizations requiring strong proton donors.
  • Enables highโ€‘efficiency catalytic cycles in petrochemical upgrading and specialty chemical production.

3. Electrolytes, Salts & Advanced Materials

  • Serves as a precursor to triflate salts, widely used in battery electrolytes, ionic liquids, and highโ€‘performance materials.
  • Used in the synthesis of metal triflates, which function as Lewis acid catalysts in green chemistry.
  • Supports development of electronic materials, including etching and doping processes in semiconductor fabrication.

4. Environmental & Green Chemistry Applications

  • Enables cleaner catalytic pathways due to its stability and low nucleophilicity, reducing byโ€‘product formation.
  • Plays a role in designing recyclable catalytic systems and solventโ€‘free reaction conditions.

5. Pharmaceutical & Biochemical Applications

  • Used in the synthesis of active pharmaceutical ingredients (APIs) requiring strong, selective protonation steps.
  • Supports formation of complex heterocycles and functionalized aromatic systems.

6. Specialty & Niche Applications

  • Functions in surface modification, fluorinated material synthesis, and precision etching in electronics manufacturing.
  • Employed in mechanistic studies involving superacidโ€‘stabilized intermediates.

Please contact us if you want to learn more or need assistance with your order.

Additional information

Weight 0.025 g
Qty

, , , , ,