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Merck

562629

Nonafluorobutane-1-sulfonic acid

97%

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

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About This Item

Linear Formula:
CF3(CF2)3SO3H
CAS Number:
Molecular Weight:
300.10
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
EC Number:
206-793-1
MDL number:
Assay:
97%
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InChI key

JGTNAGYHADQMCM-UHFFFAOYSA-N

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)

SMILES string

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

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.)

functional group

fluoro, sulfonic acid

storage temp.

2-8°C

Quality Level

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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

signalword

Danger

hcodes

Hazard Classifications

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

supp_hazards

Storage Class

8A - Combustible corrosive hazardous materials

wgk

WGK 3

flash_point_f

350.6 °F - Pensky-Martens closed cup

flash_point_c

177 °C - Pensky-Martens closed cup

ppe

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


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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)
Black D
Science of Synthesis: Houben-Weyl Methods of Molecular Transformations, 15 (2014)
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
Christopher Lau et al.
Toxicology, 441, 152522-152522 (2020-06-14)
Per- and polyfluoroalkyl substances (PFAS) are organic chemicals with wide industrial and consumer uses. They are found ubiquitously at low levels in the environment and are detectable in humans and wildlife. Perfluorobutane Sulfonate (PFBS) is a short-chained PFAS used to

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