Magic acid
Fluorosulfuric acid-antimony pentafluoride 1:1 | |
| Names | |
|---|---|
| IUPAC name
Sulfurofluoridic acid — pentafluorostiborane (1:1) | |
| Other names
Fluorosulfonyl Pentafluoroantimonic acid | |
| Identifiers | |
3D model (JSmol) |
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| ChemSpider | |
| ECHA InfoCard | 100.041.727 |
PubChem CID |
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CompTox Dashboard (EPA) |
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| Properties | |
| HSbF6SO3 | |
| Molar mass | 316.82 g/mol |
| Appearance | Liquid |
| Hazards | |
| Occupational safety and health (OHS/OSH): | |
Main hazards |
Extremely corrosive, toxic, violent hydrolysis, oxidizer. |
| GHS labelling: | |
| Danger | |
| H240, H271, H290, H302, H314, H335, H350, H402, H410, H411, H441 | |
| P234, P261, P264, P270, P271, P273, P280, P284, P301+P310, P301+P330+P331, P303+P361+P353, P304+P340+P310, P305+P351+P338+P310, P363, P390, P403+P233, 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 | |
Magic acid (FSO3H·SbF5) is a superacid consisting of a mixture, most commonly in a 1:1 molar ratio, of fluorosulfuric acid (HSO3F) and antimony pentafluoride (SbF5). This conjugate Brønsted–Lewis superacid system was developed in the 1960s by Ronald Gillespie and his team at McMaster University, and has been used by George Olah to stabilise carbocations and hypercoordinated carbonium ions in liquid media. Magic acid and other superacids are also used to catalyze isomerization of saturated hydrocarbons, and have been shown to protonate even weak bases, including methane, xenon, halogens, and molecular hydrogen.