Triethyloxonium tetrafluoroborate
| Names | |
|---|---|
| IUPAC name
Triethyloxonium tetrafluoroborate | |
| Identifiers | |
3D model (JSmol) |
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| 3598090 | |
| ChemSpider | |
| ECHA InfoCard | 100.006.096 |
PubChem CID |
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| UNII | |
| UN number | 3261 |
CompTox Dashboard (EPA) |
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| Properties | |
| [(CH3CH2)3O]+[BF4]− | |
| Molar mass | 189.99 g·mol−1 |
| Melting point | 91 to 92 °C (196 to 198 °F; 364 to 365 K) |
| Reacts | |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H314 | |
| P260, P280, P303+P361+P353, P304+P340+P310, P305+P351+P338, P310, P363 | |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
Triethyloxonium tetrafluoroborate is the organic oxonium compound with the formula [(CH3CH2)3O]+[BF4]−. It is often called Meerwein's reagent or Meerwein's salt after its discoverer Hans Meerwein. Also well known and commercially available is the related trimethyloxonium tetrafluoroborate. The compounds are white solids that dissolve in polar organic solvents. They are strong alkylating agents. Aside from the BF−4 salt, many related derivatives are available.