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This article is mainly about the principle of TEMPO free radical(2,2,6,6-tetramethylpiperidine-1-oxyl, 2564-83-2) oxidation, why the reaction can be selective and how to reduce the consumption of TEMPO. Presented by NanJing Liskon Biological Technology Co.,ltd.

TEMPO oxidizes alcohols to aldehydes and ketonesIn 1987, Anelli reported the oxidation of alcohols to aldehydes and ketones using TEMPO (CA.1% mol), NaOCl, KBr and NaHCO3 in dichloromethane - water two-phase solvent.TEMPO also called 2,2,6,6-tetramethylpiperidine-1-oxide, or 2,2,6,6-tetramethylpiper

SAN DIEGO, Aug. 19, 2021 (GLOBE NEWSWIRE) — Adamis Pharmaceuticals Corporation (Nasdaq: ADMP) today highlighted that the NIH has identified Tempol as a potential home treatment for COVID-19 (TEMPOL: A Potential Home Treatment for COVID-19 | NIH COVID-19 Research). The NIH news stated that, “This tre

A new drug of datoromycin for injection developed by Zhejiang Hisun Pharmaceutical Co.,ltd has been approved by the U.S. Food and Drug Administration(FDA). It means that the applicant can produce and sell the product in the U.S. market.Daptomycin for injection is suitable for the treatment of: 1. Co

QUESTION:TEMPO ((2,2,6,6-tetramethylpiperidin-1-yl)oxyl, or (2,2,6,6-tetramethylpiperidin-1-yl)oxidanyl),Given that it's a free radical, why doesn't it react with itself, despite being capable of reacting with other radicals in the system itself)?In addition, according to Wikipedia, it's a red-orang