Structure via PubChem · Public domain (PubChem)
Sulfolan
Sign in to saveAlso known as tetramethylene sulfone, (CH2)4SO2, tetrahydrothiophene 1-dioxide, 1,1-dioxidetetrahydrothiophene, 2,3,4,5-tetrahydrothiophene-1,1-dioxide, thiophane dioxide, thiacyclopentane dioxide
organische Schwefelverbindung, polares Lösungsmittel
Chemical data
- Formula
- C4H8O2S
- Molecular weight
- 120.17 g/mol
- IUPAC name
- thiolane 1,1-dioxide
- SMILES
- C1CCS(=O)(=O)C1
- InChIKey
- HXJUTPCZVOIRIF-UHFFFAOYSA-N
- XLogP
- -0.8
- Polar surface area
- 42.5 Ų
- H-bond donors
- 0
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Drug data · ChEMBL
- Molecule type
- Small molecule
via ChEMBL · EBI
Research
321 papers- Treatment of sulfolane in groundwater: A critical review.Journal of environmental management · 2020
- Sulfolane-Based Flame-Retardant Electrolyte for High-Voltage Sodium-Ion Batteries.Nano-micro letters · 2024
- Sulfolane-Induced Supercharging of Electrosprayed Salt Clusters: An Experimental/Computational Perspective.Journal of the American Society for Mass Spectrometry · 2021
- Ion Transport in Glyme- and Sulfolane-Based Highly Concentrated Electrolytes.Chemical record (New York, N.Y.) · 2023
- Clustering and Sorption of Sulfolane and Pyridine onto Silicates.The journal of physical chemistry. B · 2025
via PubMed
Wikidata facts
- Subclass of
- chemical compound
- Has part
- hydrogen
- Mass
- 120.025
Show 7 more facts
- canonical SMILES
- C1CCS(=O)(=O)C1
- Commons category
- Sulfolane
- found in taxon
- Batzella
- chemical formula
- C₄H₈O₂S
- boiling point
- 285
- melting point
- 27.6
- ionization energy
- 9.80
via Wikidata · CC0
Article · Deutsch
Sulfolan, systematischer Name Tetrahydrothiophen-1,1-dioxid, zählt zu den Sulfonen und ist ein polares Lösungsmittel. Das Molekül lässt sich als Fünfring aus vier Kohlenstoff-Atomen und einem doppelt oxidierten Schwefel-Atom beschreiben.
Abstract from DBpedia / Wikipedia · CC BY-SA