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Tetrabutylammonium Trifluoromethanesulfonate
PRICE INQUIRYCatalog Number
ACM35895706-2
Product Name
Tetrabutylammonium Trifluoromethanesulfonate
Structure
![{[CurrentData.Name]}](https://resource.alfachemic.com/structure/35895-70-6.gif)
CAS
35895-70-6
Synonyms
Tetrabutylammonium Triflate
Trifluoromethanesulfonic Acid Tetrabutylammonium Salt
Trifluoromethanesulfonic Acid Tetrabutylammonium Salt
IUPAC Name
tetrabutylazanium;trifluoromethanesulfonate;
Molecular Weight
391.53
Molecular Formula
C17H36F3NO3S
Canonical SMILES
CCCC[N+](CCCC)(CCCC)CCCC.C(F)(F)(F)S(=O)(=O)[O-];
InChI
1S/C16H36N.CHF3O3S/c1-5-9-13-17(14-10-6-2,15-11-7-3)16-12-8-4;2-1(3,4)8(5,6)7/h5-16H2,1-4H3;(H,5,6,7)/q+1;/p-1
InChI Key
YNJQKNVVBBIPBA-UHFFFAOYSA-M
Melting Point
113 °C
Purity
>98.0%(T)
Appearance
White to Almost white powder to crystal
Storage
Store under inert gas
Complexity
261
Covalently-Bonded Unit Count
2
EC Number
252-783-5
Exact Mass
391.237g/mol
H-Bond Acceptor
6
Heavy Atom Count
25
MDL Number
MFCD00042585
Monoisotopic Mass
391.237g/mol
Refractive Index
1.42
Rotatable Bond Count
12
Topological Polar Surface Area
65.6A^2
Application
Tetrabutylammonium Trifluoromethanesulfonate, appearing as a white to off-white crystalline powder, serves as a versatile catalyst in various chemical reactions. Its applications include facilitating the condensation of alcohols and carboxylic acids, enhancing reactions between aromatic compounds and sulfonyl chlorides, and promoting the cracking and isomerization of alkanes. Additionally, it is instrumental in the alkylation of alkenes, trans-alkylation of aromatics, trans-bromination, and other Friedel-Crafts reactions, making it an essential component in the field of organic synthesis.
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