TEMPO
| Names | |
|---|---|
| Preferred IUPAC name
(2,2,6,6-Tetramethylpiperidin-1-yl)oxyl | |
| Other names
(2,2,6,6-Tetramethylpiperidin-1-yl)oxidanyl | |
| Identifiers | |
3D model (JSmol) |
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| ChEBI | |
| ChEMBL | |
| ChemSpider | |
| ECHA InfoCard | 100.018.081 |
| EC Number |
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PubChem CID |
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| RTECS number |
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| UNII | |
CompTox Dashboard (EPA) |
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| Properties | |
| C9H18NO | |
| Molar mass | 156.249 g·mol−1 |
| Appearance | Orange-red solid |
| Melting point | 36 to 38 °C (97 to 100 °F; 309 to 311 K) |
| Boiling point | sublimes under vacuum |
| Hazards | |
| GHS labelling: | |
| Danger | |
| H314 | |
| P260, P264, P273, P280, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P321, P363, P405, P501 | |
| Safety data sheet (SDS) | External MSDS |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Infobox references | |
(2,2,6,6-Tetramethylpiperidin-1-yl)oxyl or (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl, commonly known as TEMPO, is a chemical compound with the formula (CH2)3(CMe2)2NO. This heterocyclic compound is a red-orange, sublimable solid. As a stable aminoxyl radical, it has applications in chemistry and biochemistry. TEMPO is used as a radical marker, as a structural probe for biological systems in conjunction with electron spin resonance spectroscopy, as a reagent in organic synthesis, and as a mediator in controlled radical polymerization.