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Application For the preparation of N - and O -trifluoroacetyl derivatives of a wide range of biologically active compounds for GC analysis. Also used in the oxidation of aldehydes to acids, esters, or amides.

Application For the preparation of N - and O -trifluoroacetyl derivatives of a wide range of biologically active compounds for GC analysis. Also used in the oxidation of aldehydes to acids, esters, or amides.

Application For the preparation of N - and O -trifluoroacetyl derivatives of a wide range of biologically active compounds for GC analysis. Also used in the oxidation of aldehydes to acids, esters, or amides.

Application Learn more in the Product Information Suitable for derivatization of amines, aryl amines, phenolic amines, primany amines, tertiary aromatic amines, amino acids, aminoalkylphosphoric acids, 2-aminoethylphosphoric acid,

Application Learn more in the Product Information Suitable for derivatization of amines, aryl amines, phenolic amines, primany amines, tertiary aromatic amines, amino acids, aminoalkylphosphoric acids, 2-aminoethylphosphoric acid,

Application Learn more in the Product Information Suitable for derivatization of amines, aryl amines, phenolic amines, primany amines, tertiary aromatic amines, amino acids, aminoalkylphosphoric acids, 2-aminoethylphosphoric acid,

Other Notes Please note that Sigma-Aldrich provides this product to early discovery researchers as part of a collection of unique chemicals. Sigma-Aldrich does not collect analytical data for this product.

Application Trifluoroethylene (TrFE) can be used as a monomer unit for the preparation of fluoropolymer (poly(trifluoroethylene)), which finds application in microelectronics, protective/anti-adhesive coatings, chemical industry and Li-ion

Application Reagent used in the rhodium-catalyzed &#945-trifluoromethylation of &#945,ß-unsaturated ketones. Packaging Supplied in a Sure/Pac &#8482 cylinder and has a brass needle valve with a male 1/4 NPTF outlet thread installed."

Application Reagent used in the rhodium-catalyzed &#945-trifluoromethylation of &#945,ß-unsaturated ketones. Packaging Supplied in a Sure/Pac &#8482 cylinder and has a brass needle valve with a male 1/4 NPTF outlet thread installed."

Application Trifluoromethanesulfonamide can undergo reaction with paraformaldehyde either in sulfuric acid to give the corresponding open chain and cyclic condensation products or in ethyl acetate to give the corresponding oxy-methylated products.

Application Trifluoromethanesulfonamide can undergo reaction with paraformaldehyde either in sulfuric acid to give the corresponding open chain and cyclic condensation products or in ethyl acetate to give the corresponding oxy-methylated products.