Triflic acid, >99%
Price range: $267.00 through $2,965.50
Product Code: KI-0008-HPCAS 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**
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 FriedelโCrafts 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 tertโbutyl and silyl group manipulations.
2. Catalysis in Industrial & Fine Chemical Manufacturing
- Acts as a robust, nonโoxidizing acid catalyst in pharmaceutical synthesis, improving yields and selectivity in key steps.
- Supports polymerization reactions, including cationic polymerizations requiring strong proton donors.
- Enables highโefficiency 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 highโperformance 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 byโproduct formation.
- Plays a role in designing recyclable catalytic systems and solventโfree 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 superacidโstabilized intermediates.
Please contact us if you want to learn more or need assistance with your order.





