Thermo Scientific Chemicals

Trifluoromethanesulfonic acid, 98+%, Thermo Scientific Chemicals

Catalog number: A10173.18
50 g, Each
Thermo Scientific Chemicals

Trifluoromethanesulfonic acid, 98+%, Thermo Scientific Chemicals

Catalog number: A10173.18
50 g, Each
Quantity
Informational:Informational:This chemical may require us to obtain additional information for our regulatory and chemical compliance records. If required, we will contact you for this information once your order is placed.
Catalog number: A10173.18
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Chemical Identifiers

CAS
1493-13-6
IUPAC Name
trifluoromethanesulfonic acid
Molecular Formula
CHF3O3S
InChI Key
ITMCEJHCFYSIIV-UHFFFAOYSA-N
SMILES
OS(=O)(=O)C(F)(F)F
Form
Fuming liquid
Comment
May darken on storage
Assay (unspecified)
≥98.0%
Appearance (Color)
Clear colorless to yellow

Description

Trifluoromethanesulfonic acid acts as a catalyst for esterification reactions and an acidic titrant in nonaqueous acid-base titration. It is useful in protonations due to the presence of conjugate base triflate is non nucleophilic. It serves as a deglycosylation agent for glycoproteins. In addition, it is a precursor and a catalyst in organic chemistry. It reacts with acyl halides to prepare mixed triflate anhydrides, which are strong acylating agents used in Friedel-Crafts reactions. It acts as a key starting material for the preparation of ethers and olefins by reacting with alcohols as well as to prepare trifluoromethanesulfonic anhydride by dehydration reaction.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
Trifluoromethanesulfonic acid acts as a catalyst for esterification reactions and an acidic titrant in nonaqueous acid-base titration. It is useful in protonations due to the presence of conjugate base triflate is non nucleophilic. It serves as a deglycosylation agent for glycoproteins. In addition, it is a precursor and a catalyst in organic chemistry. It reacts with acyl halides to prepare mixed triflate anhydrides, which are strong acylating agents used in Friedel-Crafts reactions. It acts as a key starting material for the preparation of ethers and olefins by reacting with alcohols as well as to prepare trifluoromethanesulfonic anhydride by dehydration reaction.

Solubility
Miscible with water, dimethyl sulfoxide, dimethyl formamide and acetonitrile.

Notes
Hygroscopic. Incompatible with strong oxidizing agents, strong bases, water and metals.
RUO – Research Use Only

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