≥96% for sensitive chromatographic and analytical workflows requiring minimal baseline interference.
Store at 2-8°C Ships Wet ice 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 0 peer-reviewed publications across chromatography, organic synthesis, and cross-coupling reactions.
Description
We are committed to bringing you Greener Alternative Products, which adhere to one or more of The 12 Principles of Greener Chemistry. This product has been enhanced for energy efficiency. Find detailshere.Allyl methyl sulfone is an organosulfur compound. It can be used as a solvent or an additive for electrochemical applications.
| Pubchem Sid | 488188062 |
|---|---|
| Sonrisas canónicas | CS(=O)(=O)CC=C |
| IUPAC Name | 3-methylsulfonylprop-1-ene |
| InChIKey | WOPDMJYIAAXDMN-UHFFFAOYSA-N |
| INCHI | 1S/C4H8O2S/c1-3-4-7(2,5)6/h3H,1,4H2,2H3 |
| Isómeros SMILES | CS(=O)(=O)CC=C |
| Peso molecular | 120.17 |
| Reaxy-Rn | 1745396 |
| Reaxys-RN_link_address | https://www.reaxys.com/reaxys/secured/hopinto.do?context=S&query=IDE.XRN=1745396&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 | Organosulfur compounds |
| Clase | Sulfonyls |
| Subclass | Sulfones |
| Intermediate Tree Nodes | Not available |
| Direct Parent | Sulfones |
| Alternative Parents | Allyl sulfur compounds Organic oxides Hydrocarbon derivatives |
| Molecular Framework | Aliphatic acyclic compounds |
| Substituents | Sulfone - Allyl sulfur compound - Organic oxygen compound - Organic oxide - Hydrocarbon derivative - Aliphatic acyclic compound |
| Descripción | This compound belongs to the class of organic compounds known as sulfones. These are compounds containing a sulfonyl group( which as the general structure RS(=O)2R' (R,R' =alkyl, aryl)) attached to two carbon atoms. |
| External Descriptors | Not available |
Find and download the COA for your product by matching the lot number on the packaging.
| Lot Number | Certificate Type | Fecha | Articulo |
|---|---|---|---|
 E2327799 | Certificate of Analysis | Mar 11, 2026 | A468089 |
| E2327802 | Certificate of Analysis | Mar 11, 2026 | A468089 |
| E2327804 | Certificate of Analysis | Mar 11, 2026 | A468089 |
| E2327803 | Certificate of Analysis | Apr 27, 2023 | A468089 |
| Índice de refracción | n20/D 1.472 |
|---|---|
| Punto de inflamación (°F) | Not applicable |
| Punto de inflamación (°C) | Not applicable |
| Peso molecular | 120.170 g/mol |
| XLogP3 | 0.200 |
| Hydrogen Bond Donor Count | 0 |
| Hydrogen Bond Acceptor Count | 2 |
| Rotatable Bond Count | 2 |
| Exact Mass | 120.025 Da |
| Monoisotopic Mass | 120.025 Da |
| Topological Polar Surface Area | 42.500 Ų |
| Heavy Atom Count | 7 |
| Formal Charge | 0 |
| Complexity | 138.000 |
| 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 |
