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Key Documents

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:
Molecular Weight:
100.07
EC Number:
MDL number:
UNSPSC Code:
12352300
PubChem Substance ID:
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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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

Signal Word

Danger

Hazard Statements

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

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Ivan Wlassics et al.
Molecules (Basel, Switzerland), 16(8), 6512-6540 (2011-08-06)
In this study we will present and discuss both the synthesis of CF(2) = CFCF(2)OSO(2)F (perfluoroallyl fluorosulfate, FAFS), focusing in particular on the important role of C(3)F(6)/SO(3) ratio, reaction temperature and boron catalyst/SO(3) ratio on FAFS' yield and selectivity, as
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
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
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

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