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419087

Sigma-Aldrich

Barium trifluoromethanesulfonate

98%

Synonym(s):

Barium triflate, Trifluoromethanesulfonic acid barium salt

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About This Item

Linear Formula:
(CF3SO3)2Ba
CAS Number:
2794-60-7
Molecular Weight:
435.47
Beilstein:
3729346
EC Number:
220-526-6
MDL number:
MFCD00143644
UNSPSC Code:
12352302
PubChem Substance ID:
24866091
NACRES:
NA.22
grade:
for analytical purposes
Pricing and availability is not currently available.

grade

for analytical purposes

Assay

98%

mp

>300 °C (lit.)

functional group

fluoro
triflate

SMILES string

[Ba++].[O-]S(=O)(=O)C(F)(F)F.[O-]S(=O)(=O)C(F)(F)F

InChI

1S/2CHF3O3S.Ba/c2*2-1(3,4)8(5,6)7;/h2*(H,5,6,7);/q;;+2/p-2

InChI key

DXJURUJRANOYMX-UHFFFAOYSA-L

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Application

Ba(CF3SO3) can be utilized as a precursor to synthesize:
  • Alkali metal and silver trifluoromethanesulfonates.[1]
  • Sodium trifluoromethanesulfonate (sodium triflate) by reacting with sodium sulfate. Sodium triflate finds application in organic synthesis as an efficient catalyst as well as a reactant in catalytic asymmetric Mannich-type reactions, and Diels-Alder reactions.[1]

Pictograms

Exclamation mark
GHS07

Signal Word

Warning

Hazard Statements

H302 + H332

Hazard Classifications

Acute Tox. 4 Inhalation - Acute Tox. 4 Oral

Storage Class Code

11 - Combustible Solids

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

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Certificates of Analysis (COA)

Lot/Batch Number
0000258586
MKBB1361V
MKBB1361
12028KI

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Sodium 1, 1, 1-Trifluoromethanesulfonate
Surya Prakash GK and Mathew T
Encyclopedia of Reagents for Organic Synthesis, Second Edition (2001)
Daniel Lundberg et al.
Physical chemistry chemical physics : PCCP, 20(21), 14525-14536 (2018-05-17)
The structures of the N,N-dimethylformamide (dmf), N,N-dimethylacetamide (dma), and N,N-dimethylpropionamide (dmp) solvated strontium and barium ions have been determined in solution using large angle X-ray scattering and EXAFS spectroscopy. The strontium ion has a mean coordination number (CN) between 6.2
Yasuyuki Muto et al.
Bioscience, biotechnology, and biochemistry, 76(11), 2162-2164 (2012-11-08)
Biotin is one of the most useful tags in (bio)analytical science due to its specific interaction with avidin, but is not easy to convert because of its low solubility in most solvents. Friedel-Crafts acylation of biotin acid chloride in triflic
Dominika Bratkowska et al.
Journal of separation science, 35(15), 1953-1958 (2012-08-07)
Two imidazolium supported ionic liquid phases (SILPs) containing different anions, trifluoromethanesulphonate [CF(3)SO(3)(-)], and tetrafluoroborate [BF(4)(-)], were synthesized and evaluated as solid-phase extraction sorbents for extracting acidic pharmaceuticals from aqueous samples under strong anion-exchange conditions, which include an effective cleanup of
Yu Hsien Lin et al.
Chemical communications (Cambridge, England), 48(88), 10910-10912 (2012-10-02)
β-Glycosyl imidinium triflate is generated from participating thioglycoside donors for disarmed-armed iterative glycosylations and one-pot oligosaccharide synthesis.
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