214000
98%
solid
reagent type: oxidant
Catalysis
Learn more about the Principles of Green Chemistry.
36-38 °C (lit.)
Aligned
2-8°C
CC1(C)CCCC(C)(C)N1[O]
1S/C9H18NO/c1-8(2)6-5-7-9(3,4)10(8)11/h5-7H2,1-4H3
QYTDEUPAUMOIOP-UHFFFAOYSA-N
Looking for similar products? Visit Product Comparison Guide
Danger
Aquatic Chronic 3 - Eye Dam. 1 - Skin Corr. 1C
8A - Combustible, corrosive hazardous materials
WGK 3
152.6 °F - closed cup
67 °C - closed cup
dust mask type N95 (US), Eyeshields, Gloves
Enter Lot Number to search for Certificate of Analysis (COA).
Enter Lot Number to search for Certificate of Origin (COO).
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.
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.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service