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Merck

88965

Supelco

Sulfolano

analytical standard

Sinónimos:

1,1-Dióxido de tetrahidrotiofeno, Tetrametilensulfona

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About This Item

Fórmula empírica (notación de Hill):
C4H8O2S
Número de CAS:
Peso molecular:
120.17
Beilstein/REAXYS Number:
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

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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

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_germany

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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Visite la Librería de documentos

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
François Versace et al.
Analytical and bioanalytical chemistry, 404(6-7), 1831-1838 (2012-08-25)
The role of busulfan (Bu) metabolites in the adverse events seen during hematopoietic stem cell transplantation and in drug interactions is not explored. Lack of availability of established analytical methods limits our understanding in this area. The present work describes

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