Date published: 2026-4-5

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Sulfolane (CAS 126-33-0)

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Alternate Names:
Tetrahydrothiophene 1,1-dioxide; Tetramethylene sulfone
CAS Number:
126-33-0
Molecular Weight:
120.17
Molecular Formula:
C4H8O2S
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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Sulfolane is a high-boiling polar aprotic solvent that is and development applications. It functions as a solvent for chemical reactions and is particularly useful for extracting aromatic hydrocarbons from hydrocarbon mixtures. Its mode of action involves its ability to dissolve a wide range of organic and inorganic compounds, making it a versatile for various experimental procedures. Sulfolane′s molecular structure allows it to interact with a variety of substances, facilitating the separation and purification of compounds in laboratory applications. Its solvent properties enable it to participate in a range of chemical processes, making it a component in experimental protocols. sulfolane plays a significant role in facilitating the manipulation and isolation of various compounds in and development .


Sulfolane (CAS 126-33-0) References

  1. Population Pharmacokinetics of Busulfan and Its Metabolite Sulfolane in Patients with Myelofibrosis Undergoing Hematopoietic Stem Cell Transplantation.  |  Dadkhah, A., et al. 2022. Pharmaceutics. 14: PMID: 35745718
  2. Difluoro(oxalato)borate's Role in the Intercalation Behavior of Mixed Anions from Sulfolane.  |  Wang, Y., et al. 2023. ChemSusChem. 16: e202201218. PMID: 36039804
  3. Theoretical Investigation of the Structure and Physicochemical Properties of Alkaline and Alkaline Earth Metal Perchlorate Solutions in Sulfolane.  |  Yusupova, AR., et al. 2022. J Phys Chem B. 126: 7676-7685. PMID: 36149734
  4. Negative Electrospray Supercharging Mechanisms of Nucleic Acid Structures.  |  Ghosh, D., et al. 2022. Anal Chem. 94: 15386-15394. PMID: 36288105
  5. Kinetic model for the dehydration of xylose to furfural from a boronate diester precursor.  |  Ricciardi, L., et al. 2022. RSC Adv. 12: 31818-31829. PMID: 36380937
  6. Energy, exergy, economic, environment, exergo-environment based assessment of amine-based hybrid solvents for natural gas sweetening.  |  Ellaf, A., et al. 2023. Chemosphere. 313: 137426. PMID: 36470356
  7. Comprehensive H2 O Molecules Regulation via Deep Eutectic Solvents for Ultra-Stable Zinc Metal Anode.  |  Li, M., et al. 2023. Angew Chem Int Ed Engl. 62: e202215552. PMID: 36536537
  8. Does Li-ion transport occur rapidly in localized high-concentration electrolytes?  |  Watanabe, Y., et al. 2023. Phys Chem Chem Phys. 25: 3092-3099. PMID: 36621826
  9. Effects of biodegradation, biotoxicity and microbial community on biostimulation of sulfolane.  |  Chang, SH., et al. 2023. Chemosphere. 319: 138047. PMID: 36739988
  10. Cage Dynamics-Mediated High Ionic Transport in Li-O2 Batteries with a Hybrid Aprotic Electrolyte: LiTFSI, Sulfolane, and N,N-Dimethylacetamide.  |  Dhananjay,. and Mallik, BS. 2023. J Phys Chem B. 127: 2991-3000. PMID: 36960946
  11. Sulfolane-containing aqueous electrolyte solutions for producing efficient ampere-hour-level zinc metal battery pouch cells.  |  Wang, Y., et al. 2023. Nat Commun. 14: 1828. PMID: 37005392
  12. Liquid-Phase Dehydration of Glycerol to Acrolein with ZSM-5-Based Catalysts in the Presence of a Dispersing Agent.  |  Huang, L., et al. 2023. Molecules. 28: PMID: 37110548
  13. Microwave-Accelerated McKenna Synthesis of Phosphonic Acids: An Investigation.  |  Mustafa, D., et al. 2023. Molecules. 28: PMID: 37110732

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

Sulfolane, 5 g

sc-251090
5 g
$23.00

Sulfolane, 100 g

sc-251090A
100 g
$21.00