reagent type: oxidant
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36-38 °C (lit.)
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Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C
8A - Combustible, corrosive hazardous materials
152.6 °F - closed cup
67 °C - closed cup
TEMPO (2,2,6,6-Tetramethylpiperidinyloxy or 2,2,6,6-Tetramethylpiperidine 1-oxyl) and its derivatives are stable nitroxy radicals used as catalysts in organic oxidation reactions. TEMPO was discovered by Lebedev and Kazarnovskii in 1960. The stable free radical nature of TEMPO is due to the presence of bulky substituent groups, which hinder the reaction of the free radical with other molecules.
he Stahl Lab focuses on the development of catalysts and catalytic reactions for selective oxidation of organic molecules, with particular emphasis on aerobic oxidation reactions.