Skip to Content
Merck
All Photos(1)

Documents

88965

Supelco

Sulfolane

analytical standard

Synonym(s):

Tetrahydrothiophene 1,1-dioxide, Tetramethylene sulfone

Sign Into View Organizational & Contract Pricing


About This Item

Empirical Formula (Hill Notation):
C4H8O2S
CAS Number:
Molecular Weight:
120.17
Beilstein:
107765
EC Number:
MDL number:
UNSPSC Code:
41116107
PubChem Substance ID:
NACRES:
NA.24

grade

analytical standard

Quality Level

vapor density

4.2 (vs air)

vapor pressure

0.01 mmHg ( 20 °C)

Assay

≥99.8% (GC)

shelf life

limited shelf life, expiry date on the label

technique(s)

HPLC: suitable
gas chromatography (GC): suitable

refractive index

n20/D 1.484 (lit.)
n20/D 1.485

bp

104 °C/0.2 mmHg (lit.)
285 °C (lit.)

mp

20-26 °C (lit.)

density

1.261 g/mL at 25 °C (lit.)

application(s)

environmental

format

neat

SMILES string

O=S1(=O)CCCC1

InChI

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

InChI key

HXJUTPCZVOIRIF-UHFFFAOYSA-N

Looking for similar products? Visit Product Comparison Guide

General description

Sulfolane is an aprotic polar solvent, used in the separation of aromatic hydrocarbons from aliphatic hydrocarbons.
Sulfolane is widely used in combination with diisopropanolamine in the sulfinol process of removal of toxic levels of hydrogen sulfide and carbonyl sulfide from raw natural gas condensate. It is also used as an industrial solvent for photographic chemicals, polymer, and petrochemical industries.

Application

Refer to the product′s Certificate of Analysis for more information on a suitable instrument technique. Contact Technical Service for further support.
Sulfolane may be used as an analytical reference standard for the quantification of the analyte in groundwater samples using gas chromatography-mass spectrometry technique.

Pictograms

Health hazardExclamation mark

Signal Word

Danger

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Repr. 1B

Storage Class Code

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

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Choose from one of the most recent versions:

Certificates of Analysis (COA)

Lot/Batch Number

Don't see the Right Version?

If you require a particular version, you can look up a specific certificate by the Lot or Batch number.

Already Own This Product?

Find documentation for the products that you have recently purchased in the Document Library.

Visit the Document Library

Industrial Solvents Handbook, Revised And Expanded (2003)
Thermochemical conversion of cellulose in polar solvent (sulfolane) into levoglucosan and other low molecular-weight substances
Kawamoto.H, et al.
Journal of Analytical and Applied Pyrolysis, 70, 303-313 (2003)
Conversion of fructose into 5-(hydroxymethyl)furfural in sulfolane.
Benjamin R Caes et al.
ChemSusChem, 4(3), 353-356 (2011-03-12)
Christopher J Hogan et al.
Physical chemistry chemical physics : PCCP, 12(41), 13476-13483 (2010-09-30)
We investigate whether "supercharging" reagents able to shift the charge state distributions (CSDs) of electrosprayed protein ions upward also influence gas-phase protein structure. A differential mobility analyzer and a mass spectrometer are combined in series (DMA-MS) to measure the mass
Kevin Aart Douglass et al.
Journal of the American Society for Mass Spectrometry, 23(3), 489-497 (2012-01-06)
The supercharging effect of sulfolane on cytochrome c (cyt c) during electrospray ionization mass spectrometry (ESI-MS) in the absence of conformational effects was investigated. The addition of sulfolane on the order of 1 mM or greater to denaturing solutions of cyt

Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.

Contact Technical Service