Ethyl methanesulfonate
| Names | |
|---|---|
| Preferred IUPAC name
Ethyl methanesulfonate | |
| Other names
Ethyl mesylate Ethyl methanesulphonate | |
| Identifiers | |
3D model (JSmol) |
|
| Abbreviations | EMS |
| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.000.488 |
| EC Number |
|
| KEGG | |
PubChem CID |
|
| UNII | |
CompTox Dashboard (EPA) |
|
| |
| |
| Properties | |
| CH3SO3C2H5 | |
| Molar mass | 124.16 g/mol |
| Appearance | Clear colorless liquid |
| Density | 1.1452 g/cm3 (22 °C) |
| Melting point | < 25 °C |
| Boiling point | 85–86 °C (185–187 °F; 358–359 K) /10 mmHg(lit) |
| Vapor pressure | 0.044 kPa @ 25˚C |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H302, H340, H351 | |
| P203, P264, P270, P280, P301+P317, P318, P330, P405, P501 | |
| NFPA 704 (fire diamond) | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Ethyl methanesulfonate (EMS) is an organosulfur compound with the formula CH3SO3C2H5. It is the ethyl ester of methanesulfonic acid. A colorless liquid, it is classified as an alkylating agent. EMS is the most commonly used chemical mutagen in experimental genetics. Mutations induced by EMS exposure can then be studied in genetic screens or other assays.