4-Oxo-2,2,6,6-tetramethylpiperidinooxy Basic information |
Product Name: | 4-Oxo-2,2,6,6-tetramethylpiperidinooxy |
Synonyms: | 4-Oxo-2,2,6,6-tetramethyl-1-piperidinyloxy, free radical;4-OXO-TEMPO, FREE RADICAL 80+%;4-OXO-TEMPO, FREE RADICAL 99+%;4-OXO-2,2,6,6-TETRAMETHYLPIPERIDINOXY;4-Oxo-2,2,6,6-tetramethylpiperidine-1-oxyl(4-Oxo-TEMPO,freeradical);4-Oxo-2,2,6,6;4-Oxo-2,2,6,6-trtramethyl-1-piperidi nyloxy,free radical;2,2,6,6-Tetramethyl-4-piperidone 1-oxyl, free radical |
CAS: | 2896-70-0 |
MF: | C9H16NO2* |
MW: | 170.23 |
EINECS: | 220-778-7 |
Product Categories: | Industrial/Fine Chemicals;Spin Labeling Compounds;Analytical Chemistry;ESR Spectrometry;Spin Labels |
Mol File: | 2896-70-0.mol |
4-Oxo-2,2,6,6-tetramethylpiperidinooxy Chemical Properties |
Melting point | 33-38 °C |
Boiling point | 299.88°C (rough estimate) |
density | 1.0710 (rough estimate) |
vapor pressure | 2.254Pa at 25℃ |
refractive index | 1.4640 (estimate) |
storage temp. | 2-8°C |
form | Needles, Crystals or Crystalline Powder |
color | Orange |
Water Solubility | Soluble in water (partly), acetone, DMSO, 100% ethanol, and diethylether. Insoluble in water. |
BRN | 1818579 |
LogP | 0.28 at 22℃ |
CAS DataBase Reference | 2896-70-0(CAS DataBase Reference) |
NIST Chemistry Reference | 1-Piperidinyloxy, 2,2,6,6-tetramethyl-4-oxo-(2896-70-0) |
EPA Substance Registry System | 1-Piperidinyloxy, 2,2,6,6-tetramethyl-4-oxo- (2896-70-0) |
Safety Information |
Risk Statements | 36/37/38 |
Safety Statements | 24/25 |
RIDADR | UN 3077 9 / PGIII |
WGK Germany | 3 |
RTECS | TN9200000 |
TSCA | Yes |
HS Code | 29333990 |
MSDS Information |
Provider | Language |
---|---|
4-Oxo-TEMPO | English |
ACROS | English |
SigmaAldrich | English |
ALFA | English |
4-Oxo-2,2,6,6-tetramethylpiperidinooxy Usage And Synthesis |
Description | 2,2,6,6-Tetramethylpiperidin-1-oxyl (TEMPO) is a stable radical that will react with reactive oxygen species (ROS). This conversion, followed by ESR, provides an indirect way to monitor ROS production in biological systems. TEMPONE is the 4-oxo derivative of TEMPO. In addition to possible uses as a spin trap, this nitroxyl radical can be used in hydrogen transfer experiments and as a polarizing agent in dynamic nuclear polarization NMR spectroscopy. TEMPONE and other nitroxyl radicals have also been shown to reduce mean arterial pressure in spontaneously hypertensive rats when administered intravenously. |
Chemical Properties | Pink Needles |
Uses | A spin label for ESR studies |
Uses | Free-radical nitroxide spin probe typically used for:
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General Description | 4-Oxo-TEMPO is formed by the reaction of 2,2,6,6-tetramethyl-4-piperidone (4-oxo-TMP) and 1O2. It is a stable paramagnetic product formed during the irradiation of TiO2 in aqueous suspensions. |
Flammability and Explosibility | Nonflammable |
4-Oxo-2,2,6,6-tetramethylpiperidinooxy Preparation Products And Raw materials |
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