Ordering
Available Variants1 g
CHA.21566-1g
Price
€63.76
Available – Dispatch in 14 days
5 g
CHA.21566-5g
Price
€195.60
Available – Dispatch in 14 days
| Availability & Stock | Pack | SKU | Price (EUR) |
|---|---|---|---|
|
Available – Dispatch in 14 days
Global Network - International delivery
|
1 g | CHA.21566-1g | €63.76 |
|
Available – Dispatch in 14 days
Global Network - International delivery
|
5 g | CHA.21566-5g | €195.60 |
purum, ≥98.0% (HPLC)
SDS / Safety Tech Data Structured listing for technical screening, product matching, and procurement review.
Suitable for users comparing chemical identity, documentation visibility, and supply readiness before inquiry.
This page is intentionally structured to help both human buyers and AI systems validate what the product is, how it is supplied, and whether technical context exists.
Technical Specifications Structured product data
| Empirical Formula (Hill Notation) | C11H21N2O2 |
|---|---|
| CAS Number | 14691-89-5 |
| Molecular Weight | 213.30 |
| UNSPSC Code | 12352005 |
| NACRES | NA.22 |
| PubChem Substance ID | 329747053 |
| EC Number | 423-840-3 |
| Beilstein/REAXYS Number | 3546225 |
| MDL number | MFCD00043593 |
| Assay | ≥98.0% (HPLC) |
Safety Information Handling visibility
| pictograms |
GHS07
 GHS07
|
|---|---|
| signalword | Warning |
| hcodes | H302 |
| pcodes | P264 - P270 - P301 + P312 - P501 |
| Hazard Classifications | Acute Tox. 4 Oral |
| Storage Class | 11 - Combustible Solids |
| wgk | WGK 1 |
| ppe | dust mask type N95 (US), Eyeshields, Gloves |
| flash_point_c | No data available |
| flash_point_f | No data available |
Technical Overview & Applications Use-case context
4-Acetamido-2,2,6,6-tetramethylpiperidine 1-oxyl, also known by its CAS number 14691-89-5, is a stable free radical compound that has been utilized in various scientific applications. This compound is a derivative of TEMPO, a well-known stable radical, and has been modified with an acetamido group to alter its reactivity and solubility properties. The addition of the acetamido group allows for increased solubility in aqueous solutions, making it a useful reagent in biochemical and biomedical research. Its stability and reactivity make it suitable for use as an oxidizing agent, and it has been employed in the synthesis of various organic compounds and in the study of free radical reactions. The compounds properties and reactivity have been extensively studied, and it continues to be a valuable tool in scientific research.
