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236535

Sigma-Aldrich

Fluorosulfonic acid

purified by triple-distillation

Synonym(s):

Fluosulfuric acid

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About This Item

Linear Formula:
FSO3H
CAS Number:
7789-21-1
Molecular Weight:
100.07
EC Number:
232-149-4
MDL number:
MFCD00066174
UNSPSC Code:
12352300
PubChem Substance ID:
24854177
NACRES:
NA.23

vapor density

3.5 (vs air)

vapor pressure

2.5 mmHg ( 25 °C)

purified by

triple-distillation

bp

165.5 °C (lit.)

mp

−87.3 °C (lit.)

density

1.726 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

OS(F)(=O)=O

InChI

1S/FHO3S/c1-5(2,3)4/h(H,2,3,4)

InChI key

UQSQSQZYBQSBJZ-UHFFFAOYSA-N

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Related Categories

Application

  • Polymerization of epoxidized triglycerides with fluorosulfonic acid: The article investigates the use of fluorosulfonic acid for the cationic polymerization of epoxidized triglycerides, exploring its potential in polymer chemistry (Biswas et al., 2016).

Packaging

Packaged in PFA/FEP bottles

Pictograms

CorrosionExclamation mark
GHS05,GHS07

Signal Word

Danger

Hazard Statements

H314,H332

Hazard Classifications

Acute Tox. 4 Inhalation - Skin Corr. 1A

Storage Class Code

8A - Combustible corrosive hazardous materials

WGK

WGK 1

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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Leslie Dos Santos et al.
Membranes, 10(10) (2020-09-27)
Electrospinning was employed to fabricate composite membranes containing perfluorosulfonic acid (PFSA) ionomer, poly(vinylidene fluoride) (PVDF) reinforcement and a sulfonated silica network, where the latter was incorporated either in the PFSA matrix or in the PVDF fibers. The best membrane, in
Roger L Snowden
Chemistry & biodiversity, 5(6), 958-969 (2008-07-12)
Using a novel, acid-mediated cyclization methodology, a direct access to Cetalox ((+/-)-1; a commercially important ambergris-type odorant) and various structurally related didehydro (i.e., 19, 26, and 30) and tetradehydro (i.e., 28 and 37/38) analogues is described. Treatment of either (E,E)-14
F Renosto et al.
The Journal of biological chemistry, 262(34), 16279-16288 (1987-12-05)
ATP sulfurylase from Penicillium chrysogenum is a noncooperative homooligomer containing three free sulfhydryl groups per subunit. Under nondenaturing conditions, one SH group per subunit was modified by 5,5'-dithiobis-(2-nitrobenzoate), or N-ethylmaleimide. Modification had only a small effect on kcat, but markedly
Xiaolu Li et al.
Analytica chimica acta, 1122, 31-38 (2020-06-07)
An upright GO (UGO) modified screen-printed electrode was prepared with the help of the external magnetic field for improving its electrochemical performance. The ratio of GO: Nafion and the magnetic field intensity on the properties of UGO were examined by
P A Seubert et al.
Archives of biochemistry and biophysics, 240(2), 509-523 (1985-08-01)
The kinetics of the forward ATP sulfurylase-catalyzed reaction were examined using a new assay based on 32PPi released from [gamma-32P]MgATP in the presence of inorganic sulfate. Replots yielded Vmaxf = 6.6 units mg protein-1, KmA = 0.13 mM, Kia =
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