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Merck
CN

T22209

Sulfolane

99%

Synonym(s):

Tetrahydrothiophene 1,1-dioxide, Tetramethylene sulfone

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About This Item

Empirical Formula (Hill Notation):
C4H8O2S
CAS Number:
Molecular Weight:
120.17
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
EC Number:
204-783-1
Beilstein/REAXYS Number:
107765
MDL number:
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Product Name

Sulfolane, 99%

InChI key

HXJUTPCZVOIRIF-UHFFFAOYSA-N

InChI

1S/C4H8O2S/c5-7(6)3-1-2-4-7/h1-4H2

SMILES string

O=S1(=O)CCCC1

vapor density

4.2 (vs air)

vapor pressure

0.01 mmHg ( 20 °C)

assay

99%

refractive index

n20/D 1.484 (lit.)

bp

104 °C/0.2 mmHg (lit.)
285 °C (lit.)

mp

20-26 °C (lit.)

density

1.261 g/mL at 25 °C (lit.)

Quality Level

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Application

Sulfolane is a polar aprotic solvent that may be used for the complete pyrolysis of cellulose without any polymerization or carbonization side reaction. Sulfolane, in combination with mesitylene, can be used as a solvent in the synthesis of poly(succinimide) (PSI) from L-aspartic acid. It can also be used as a solvent in the synthesis of chlorine-terminated polyethersulfone oligomer, a polymeric activator for nylon 6-polyethersulfone (PES)-nylon 6 block copolymer synthesis.

pictograms

Health hazardExclamation mark

signalword

Danger

Hazard Classifications

Acute Tox. 4 Oral - Repr. 1B

Storage Class

6.1C - Combustible acute toxic Cat.3 / toxic compounds or compounds which causing chronic effects

wgk

WGK 1

flash_point_f

350.6 °F - closed cup

flash_point_c

177 °C - closed cup

ppe

dust mask type N95 (US), Eyeshields, Gloves


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Self-aggregates of hydrophobically modified poly (2-hydroxyethyl aspartamide) in aqueous solution.
Yang SR
Coll. Polymer Sci., 281(9), 852-861 (2003)
Nylon 6-polyethersulfone-nylon 6 block copolymer: synthesis and application as compatibilizer for polyethersulfone/nylon 6 blend.
Ahn TO
Polymer, 38(1), 207-215 (1997)
Christopher Paul Kasanke et al.
Scientific reports, 9(1), 3121-3121 (2019-03-01)
Sulfolane is an industrial solvent and emerging organic contaminant affecting groundwater around the world, but little is known about microbes capable of biodegrading sulfolane or the pathways involved. We combined DNA-based stable isotope probing (SIP) with genome-resolved metagenomics to identify
Polymer micelle-like aggregates of novel amphiphilic biodegradable poly (asparagine) grafted with poly (caprolactone).
Jeong JH
Polymer, 44(3), 583-591 (2003)
Thermochemical conversion of cellulose in polar solvent (sulfolane) into levoglucosan and other low molecular-weight substances.
Kawamoto H
Journal of Analytical and Applied Pyrolysis, 70(2), 303-313 (2003)

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