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Sigma-Aldrich

Nonafluorobutane-1-sulfonic acid

97%

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Synonym(s):
1,1,2,2,3,3,4,4,4-Nonafluoro-1-butanesulfonic acid, 1-Perfluorobutanesulfonic acid, Nonafluoro-1-butanesulfonic acid, Nonafluorobutan-1-sulfonic acid, Nonafluorobutanesulfonic acid, Perfluorobutanesulfonic acid, n-Nonafluorobutanesulfonic acid
Linear Formula:
CF3(CF2)3SO3H
CAS Number:
Molecular Weight:
300.10
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Quality Level

Assay

97%

refractive index

n20/D 1.3230 (lit.)

bp

112-114 °C/14 mmHg (lit.)

density

1.811 g/mL at 25 °C (lit.)

storage temp.

2-8°C

SMILES string

OS(=O)(=O)C(F)(F)C(F)(F)C(F)(F)C(F)(F)F

InChI

1S/C4HF9O3S/c5-1(6,3(9,10)11)2(7,8)4(12,13)17(14,15)16/h(H,14,15,16)

InChI key

JGTNAGYHADQMCM-UHFFFAOYSA-N

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General description

Nonafluorobutane-1-sulfonic acid is a colorless liquid that can be considered as a superacid, which can be synthesized by reacting 1-iodononafluorobutane with sodium dithionite in the presence of sodium bicarbonate in acetonitrile/water.

Application

Nonafluorobutane-1-sulfonic acid may be used as catalyst in the synthesis of 6-chloro-6H-dibenz[c,e][1,2]oxaphosphorin and N-benzylpyridin-2-amine.

Pictograms

CorrosionExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Eye Dam. 1 - Skin Corr. 1B

Supplementary Hazards

WGK

WGK 3

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

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Black D
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 15 (2014)
Lizhu Tang et al.
Chemosphere, 256, 127169-127169 (2020-05-29)
Parental exposure to perfluorobutane sulfonate (PFBS), an aquatic pollutant of emerging concern, is previously found to impair the embryonic development of offspring. However, the impairing mechanisms remain to clarify. In the present study, adult zebrafish were exposed to 0, 10
"A general method for the preparation of perfluoroalkanesulfonyl chlorides"
Scott.H.J P, et al.
Journal of Fluorine Chemistry, 126(8), 1196-1201 (2005)
"Superacid-catalyzed Friedel?Crafts phosphination of 2-hydroxybiphenyls with phosphorus trichloride"
Ito T, et al.
Heteroatom Chem., 27(5), 336-342 (2016)
Yiren Yue et al.
Food and chemical toxicology : an international journal published for the British Industrial Biological Research Association, 145, 111695-111695 (2020-08-25)
Perfluorobutanesulfonic acid (PFBS), a shorter chain Per- and polyfluoroalkyl substances (PFASs) cognate of perfluorooctanesulfonic acid (PFOS), has been used as replacement for the toxic surfactant PFOS. However, emerging evidences suggest safety concerns for PFBS and its effect on reproductive health

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