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4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-Oxyl Benzoate Free Radical [Catalyst for Oxidation]

Catalog Number
ACM3225261-1
Product Name
4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-Oxyl Benzoate Free Radical [Catalyst for Oxidation]
Structure
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CAS
3225-26-1
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Synonyms
4-Hydroxy-TEMPO Benzoate Free Radical
4-Benzoyloxy-2,2,6,6-tetramethylpiperidine 1-Oxyl Free Radical
4-Benzoyloxy-TEMPO Free Radical
IUPAC Name
(1-λ1-oxidanyl-2,2,6,6-tetramethylpiperidin-4-yl) benzoate;
Molecular Weight
276.36
Molecular Formula
C16H22NO3
Canonical SMILES
CC1(CC(CC(N1[O])(C)C)OC(=O)C2=CC=CC=C2)C;
InChI
InChI=1S/C16H22NO3/c1-15(2)10-13(11-16(3,4)17(15)19)20-14(18)12-8-6-5-7-9-12/h5-9,13H,10-11H2,1-4H3
InChI Key
MJEDTBDGYVATPI-UHFFFAOYSA-N
Melting Point
104 °C
Purity
>97.0%(GC)(T)
Appearance
Light yellow to Brown powder to crystal
Storage
Store under inert gas
Complexity
341
Covalently-Bonded Unit Count
1
Exact Mass
276.16g/mol
H-Bond Acceptor
3
Heavy Atom Count
20
MDL Number
MFCD00075563
Monoisotopic Mass
276.16g/mol
Rotatable Bond Count
3
Topological Polar Surface Area
30.5A^2
Application
The purpose of 4-Hydroxy-2,2,6,6-tetramethylpiperidine 1-Oxyl Benzoate Free Radical as a catalyst for oxidation is to facilitate the conversion of alcohols into aldehydes, ketones, and carboxylic acids without the need for catalytic or stoichiometric heavy metal oxidants. This product acts as a recyclable catalyst within a hypochlorite/bromite-nitroxide system, providing an efficient and environmentally friendly alternative for oxidation processes. As a derivative of 4-substituted 2,2,6,6-tetramethylpiperidyl-1-oxy (TEMPO), it exists as an orange crystalline powder, emphasizing its role in sustainable chemical transformations.
April 15, 2025

A Game-Changer in Oxidation Catalysis

Using Alfa Chemistry's 4-Hydroxy-TEMPO Benzoate has simplified our lab's oxidation processes. Its efficiency in alcohols to carbonyls conversion, without heavy metals, proved invaluable in our research applications. Highly recommend for precise, sustainable experiments.

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