4-Oxo-TEMPO-d16,1-15N, free radical
4-Oxo-TEMPO-d16,1-15N, free radical (CAS: 80404-14-4) is a deuterated and nitrogen-15 labelled derivative of the stable nitroxyl radical TEMPO. With a molecular weight of 187.32 g/mol, this compound is specifically prepared for Electron Spin Resonance (ESR) spectroscopy. Its isotopic labelling enhances spectral resolution and provides unique analytical capabilities in various research applications, particularly in studies involving radical chemistry and spin labelling.
- IUPAC
- 4-Oxo-2,2,6,6-tetramethylpiperidine-d16,1-15N-1-oxyl,TEMPONE-d16,1-15N
- Synonyms
- 80404-14-4C9D1615NO24-Oxo-2,2,6,6-tetramethylpiperidine-d16,1-15N-1-oxylTEMPONE-d16,1-15N

ESR Spectroscopy
Utilised as a spin probe or spin label in Electron Spin Resonance (ESR) spectroscopy due to its stable radical nature and isotopic enrichment. The deuterium and 15N labelling allows for fine-tuning spectral parameters and enhancing sensitivity in complex biological and chemical systems.
Isotopic Labelling Studies
Serves as a valuable tool in mechanistic studies where isotopic tracing is required. The precisely labelled atoms enable researchers to track the fate of the TEMPO moiety in chemical reactions and biological processes with high accuracy.
Chemical Synthesis
Can be employed as a reagent in organic synthesis, leveraging its properties as a stable radical and an oxidising agent, with the added benefit of isotopic markers for reaction pathway elucidation.
| Molecular weight | 187.32 |
|---|---|
| Empirical formula | C9D1615NO2 |
| Grade | for ESR-spectroscopy |
| Melting point | 35 °C(lit.) |
| Mol Wt | mol wt 186.98 by atom % calculation |
|---|---|
| Isotopic Purity | 98 atom % 15N98 atom % D |
| Mass Shift | M+17 |
Documentation
Every batch ships with a Certificate of Analysis covering assay, identity and purity; the grade is confirmed against your enquiry. Safety Data Sheets and technical data sheets are available on request.
Supply & logistics
Samples for technical evaluation; bulk MOQ by grade and packaging. In-stock material ships in 7–10 working days, worldwide, with full export documentation.
What is 4-Oxo-TEMPO-d16,1-15N, free radical used for?
+
This compound is primarily used for ESR spectroscopy as a spin probe or label, and in chemical synthesis for mechanistic studies requiring isotopic tracing.
What are the CAS number and molecular formula?
+
The CAS number is 80404-14-4. The empirical formula is C9D1615NO2.
What grade and purity does Tech Serve Solutions supply?
+
Tech Serve Solutions supplies this product for ESR spectroscopy, with isotopic purity of 98 atom % 15N and 98 atom % D. TSS does not represent this product as USP, BP, EP or other pharmacopoeial grades.
How should 4-Oxo-TEMPO-d16,1-15N, free radical be handled?
+
It is classified as hazardous with Water Hazard Class 3 (WGK 3) in Germany. Handle with appropriate personal protective equipment in a well-ventilated area to avoid exposure.
How is this chemical packed, shipped, and exported?
+
Tech Serve Solutions expertly packs and ships chemicals globally, adhering to all relevant regulations for safe international transit. Contact us for specific shipping details.
How can I request a quote or sample?
+
Please contact our sales team via the website or direct email to request a quotation or a sample for evaluation.
▶ Related products

1-(2-Fluorobenzyl)piperazine
C11H15FN2
Chemical Synthesis
1-(2-Fluorophenyl)biguanide hydrochloride
Chemical Synthesis

1-(2-Fluorophenyl)cyclopropanecarboxylic acid
C10H9FO2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine
C10H13FN2
Chemical Synthesis
1-(2-Fluorophenyl)piperazine monohydrochloride
C10H13FN2 · HCl
Chemical Synthesis
1-(2-Furoyl)-1H-benzotriazole
C11H7N3O2
Chemical Synthesis
1-(2-Furoyl)piperazine
C9H12N2O2
Chemical Synthesis
1-(2-Hydroxy-5-methylphenyl)-3-phenyl-1,3-propanedione
Chemical Synthesis
▶ Explore more

3-Methyl-1,5-di-p-tolyl-1,4-pentazadiene
Chemical Synthesis

3-Methyl-1,5-pentanediol
Chemical Synthesis

3-Methyl-1-(2-methylphenyl)-1H-pyrazol-5-amine
C11H13N3
Chemical Synthesis
3-Methyl-1-(3′-sulfoamidophenyl)-5-pyrazolone
C10H11N3O3S
Chemical Synthesis