1 M in THF for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Room temperature Ships Check lot-specific COA for exact specifications.
SDS, COA, datasheet, and spec sheet available for download. Lot-specific COA accessible via lot number lookup.
Cited in 286 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Application
Valuable building block or solvent offered as a solution in tetrahydrofuran for more convenient handling. 1,3.Flammable liquid-Propanesultone has been used in: preparation of poly[2-ethynyl- N -(propylsulfonate)pyridinium betaine], a new ionic conjugated polymer preparation of novel poly(4-vinylpyridine) supported acidic ionic liquid catalyst preparation of poly((2-(dimethylamino)ethyl methacrylate)-co-3.Flammable liquid-dimethyl(methacryloyloxyethyl)ammonium propanesulfonate)-coated mesoporous silica nanoparticles sulfonation of surface of self-assembled nanoporous silica colloidal crystalline films comprised of 184nm-diameter silica spheres
| Canonical Smiles | C1COS(=O)(=O)C1 |
|---|---|
| IUPAC Name | oxathiolane 2,2-dioxide |
| InChIKey | FSSPGSAQUIYDCN-UHFFFAOYSA-N |
| INCHI | 1S/C3H6O3S/c4-7(5)3-1-2-6-7/h1-3H2 |
| Isomeric SMILES | C1COS(=O)(=O)C1 |
| WGK Germany | 3 |
| RTECS | RP5425000 |
| UN Number | 2810 |
| Packing Group | I |
| Molecular Weight | 122.14 |
| Beilstein | 109782 |
| Reaxy-Rn | 109782 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=109782&ln= |
Comprehensive hazard, handling, storage, and regulatory compliance document.
Download SDS →Lot-specific quality data. Enter your lot number to retrieve the exact COA.
Look up COA →Full quality attributes and acceptance criteria for this grade.
View spec sheet →Taxonomy Tree
| Kingdom | Organic compounds |
|---|---|
| Superclass | Organoheterocyclic compounds |
| Class | Oxathiolanes |
| Subclass | Gamma sultones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Gamma sultones |
| Alternative Parents | Sulfonic acid esters Organosulfonic acid esters Oxacyclic compounds Organooxygen compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic heteromonocyclic compounds |
| Substituents | Gamma-sultone - Organosulfonic acid ester - Sulfonic acid ester - Organosulfonic acid or derivatives - Organic sulfonic acid or derivatives - Oxacycle - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Organooxygen compound - Aliphatic heteromonocyclic compound |
| Description | This compound belongs to the class of organic compounds known as gamma sultones. These are organic compounds containing a gamma-sultone, a Intramolecular cyclic ester of hydroxy sulfonic acid, with a SO ring bond, and three ring carbon atoms. |
| External Descriptors | sultone |
| Freezing Point(°C) | 32 °C |
|---|---|
| Flash Point(°F) | >230 °F |
| Flash Point(°C) | >110 °C |
| Boil Point(°C) | 180 °C/30 mmHg |
| Melt Point(°C) | 32°C |
| Molecular Weight | 122.150 g/mol |
| XLogP3 | -0.200 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 3 |
| Rotatable Bond Count | 0 |
| Exact Mass | 122.004 Da |
| Monoisotopic Mass | 122.004 Da |
| Topological Polar Surface Area | 51.800 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 140.000 |
| Isotope Atom Count | 0 |
| Defined Atom Stereocenter Count | 0 |
| Undefined Atom Stereocenter Count | 0 |
| Defined Bond Stereocenter Count | 0 |
| Undefined Bond Stereocenter Count | 0 |
| The total count of all stereochemical bonds | 0 |
| Covalently-Bonded Unit Count | 1 |
