2,2,6,6-Tetramethylpiperidine 1-Oxyl Free Radical (CAS 2564-83-2) is a high-quality chemical from TCI, supplied as GC Grade / for Synthesis.
Application: Six-membered heterocyclic compound used in the synthesis of pharmaceuticals, ligands, and bioactive compounds.
Specifications:
- Molecular formula: C9H18NO
- CAS number: 2564-83-2
- Purity: >98.0%(GC)(T)
- TCI product code: T1560
Synonyms: TEMPO Free Radical
Available from AMI Scientific, the authorised TCI distributor in Indonesia. Contact us for pricing and stock availability — we ship throughout Indonesia.
TCI brochures (PDF)
- Crystalline Hypochlorite Salt with Ease of Handling 2025-06-17 · p. 1
- Highly Active Catalyst for Alcohol Oxidation - AZADOL® 2024-07-03 · p. 2
- Organic Radical Magnets 2024-11-27 · p. 1
- Oxidizing Agents 2025-06-11 · p. 2
- Battery Research Reagents 2026-09-18 · p. 7
- C-H Bond Activation Reaction 2025-06-20 · p. 10
Related TCI products
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- TCI G0555 122413-85-8 4-Glycidyloxy-2,2,6,6-tetramethylpiperidine 1-Oxyl Free Radical
- TCI C1406 2154-68-9 3-Carboxy-2,2,5,5-tetramethylpyrrolidine 1-Oxyl Free Radical
- TCI H1404 1155843-79-0 2-Hydroxy-2-azaadamantane
- TCI B0643 106-95-6 Allyl Bromide
- TCI T0431 76-05-1 Trifluoroacetic Acid
From the TCI brochure
- 0.013 eq (S0939 1.2 eq, Bu4NHSO4 0.05 eq, CH2Cl2, 5 °C)
- 0.01 eq (S0939 1.6 eq, Bu4NHSO4 0.05 eq, CH2Cl2, 15 °C)
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Data from the TCI brochure
| Massa dan jumlah mol pada prosedur | 21 mg, 0.13 mmol (2-octanol 1.30 g (10.0 mmol), NaOCl·5H2O 2.0 g (12.2 mmol), CH2Cl2 10 mL, 5 °C, 0.5 h) |
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Source: TCI brochure RR064 (2025-06-17)
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References cited in the TCI brochure
- Yoshikazu Kimura. Sodium Hypochlorite Pentahydrate (NaOCl·5H2O) Crystals as an Extraordinary Oxidant for Primary and Secondary Alcohols Synlett, 2014. doi:10.1055/s-0033-1340483
- Masaki Hayashi. 9-Azanoradamantane N-Oxyl (Nor-AZADO): A Highly Active Organocatalyst for Alcohol Oxidation Chemical and Pharmaceutical Bulletin, 2011. doi:10.1248/cpb.59.1570
- Yoshiharu Iwabuchi. Practical Preparation Methods for Highly Active Azaadamantane-Nitroxyl-Radical-Type Oxidation Catalysts Synthesis, 2011. doi:10.1055/s-0030-1260257
- Masaki Hayashi. Oxidation of Alcohols to Carbonyl Compounds with Diisopropyl Azodicarboxylate Catalyzed by Nitroxyl Radicals The Journal of Organic Chemistry, 2012. doi:10.1021/jo300088b
Product Categories
- Catalysis and Inorganic ChemistryOrganocatalysts [Catalysis]Oxidation Organocatalysts
- Catalysis and Inorganic ChemistryOxidation [Catalysis]Oxidation Organocatalysts
- Chemical BiologyGlycoscienceReagents for Oligosaccharide Synthesis [Glycoscience]
- Synthetic ReagentsOxidation [Synthetic Reagents]Oxidants (Other) [Oxidation]
- Synthetic ReagentsRadical ChemistryStable Radicals [Synthetic Reagents]
- Synthetic ReagentsC-X(Non-Halogen) Bond Formation [Synthetic Reagents]C-H Bond Activation Reaction [Synthetic Reagents]
- Battery MaterialsOrganic Redox Flow Battery Materials [Battery Materials]Organic Radicals [Battery Materials]
- Electronic MaterialsBattery MaterialsOrganic Redox Flow Battery Materials [Battery Materials]
- Magnetic MaterialsOrganic Radicals [Magnetic Materials]
- Polymer/Macromolecule ReagentsPolymerization ReagentsControlled Radical Polymerization Reagents
- Biomaterials/Biocompatible Materials Research ReagentsPolymerization Reagents (Initiators, Catalysts, Ligands) [Biomaterials/Biocompatible Materials Research Reagents]Nitroxide-Mediated Radical Polymerization (NMP) Reagents








