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Key Documents

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236535

Sigma-Aldrich

Fluorosulfonic acid

purified by triple-distillation

Sinónimos:

Fluosulfuric acid

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About This Item

Fórmula lineal:
FSO3H
Número de CAS:
7789-21-1
Peso molecular:
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)

Quality Level

100

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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Categorías relacionadas

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

signalword

Danger

hcodes

H314,H332

Hazard Classifications

Acute Tox. 4 Inhalation - Skin Corr. 1A

Storage Class

8A - Combustible corrosive hazardous materials

wgk_germany

WGK 1

flash_point_f

Not applicable

flash_point_c

Not applicable

ppe

Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter

Certificados de análisis (COA)

Busque Certificados de análisis (COA) introduciendo el número de lote del producto. Los números de lote se encuentran en la etiqueta del producto después de las palabras «Lot» o «Batch»

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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
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
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
Y Takeuchi et al.
Chemical & pharmaceutical bulletin, 45(6), 1085-1088 (1997-06-01)
In order to develop novel methods for electrophilic and enantioselective fluorination of active methine compounds, preliminary experiments were carried out. The N-tosyl derivative 5 obtained from D-phenylglycine was fluorinated with FClO3 or diluted F2 gas to give the N-fluoro-N-tosyl derivative
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