Galvinoxyl
 | |
| Properties | |
|---|---|
| C29H41O2 | |
| Molar mass | 421.65 g·mol−1 |
| Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). | |
| Infobox references | |
Galvinoxyl is a commercially available free radical inhibitor. It may be synthesized by oxidation of the parent phenol with lead dioxide or potassium hexacyanoferrate(III). Its radical structure is confirmed by the loss of the O-H stretch in the IR spectrum and by electron spin resonance; it is stable even in the presence of oxygen.[1][2]
References
- ↑ Coppinger, Galvin M. (1957). "A Stable Phenoxy Radical Inert to Oxygen". J. Am. Chem. Soc. 79 (2): 501. doi:10.1021/ja01559a073.
- ↑ Kharasch, M. S.; Joshi, B. S. (1957). "Reactions of Hindered Phenols. II. Base-Catalyzed Oxidations of Hindered Phenols". J. Am. Chem. Soc. 22 (11): 1439. doi:10.1021/jo01362a034.
This article is issued from Wikipedia - version of the 7/7/2015. The text is available under the Creative Commons Attribution/Share Alike but additional terms may apply for the media files.