4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy

4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy
  • CAS No.:2226-96-2
Other grades of this product :

4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy Basic information
Product Name:4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy
Synonyms:HYDROXY-TEMPO;4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINE-N-OXYL;4-HYDROXY-2,2,6,6-TETRAMETHYL-PIPERIDINOOXY;4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINE 1-OXYL;4-HYDROXY-2,2,6,6-TETRAMETHYL-1-PIPERIDIN-1-YLOXY;4-HYDROXY-2,2,6,6-TETRAMETHYL-1-PIPERIDINYLOXY, FREE RADICAL;4-HYDROXY-2,2,6,6-TETRAMETHYL-PIPERIDINOOXY, FREE RADICAL;4-HYDROXY-2,2,6,6-TETRAMETHYLPIPERIDINYLOXY
CAS:2226-96-2
MF:C9H18NO2*
MW:172.24
EINECS:218-760-9
Product Categories:Inhibitors;Analytical Chemistry;ESR Spectrometry;Spin Labels;Heterocycles;Nitric Oxide Reagents;Spin Labeling Compounds
Mol File:2226-96-2.mol
4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy Chemical Properties
Melting point 69-71 °C(lit.)
Boiling point 302.58°C (rough estimate)
density 1.0402 (rough estimate)
vapor pressure 0.025Pa at 20℃
refractive index 1.4350 (estimate)
Fp 146°(295°F)
storage temp. 2-8°C
solubility 1670g/l
form Crystals or Crystalline Powder
pka5.07[at 20 ℃]
color Orange
PH8.2 (20g/l, H2O, 20℃)
Water Solubility soluble
Merck 14,9141
BRN 1422990
Stability:Stable. Incompatible with strong oxidizing agents.
InChIKeyFAPCFNWEPHTUQK-UHFFFAOYSA-N
LogP0.56 at 25℃
CAS DataBase Reference2226-96-2(CAS DataBase Reference)
NIST Chemistry Reference1-Piperidinyloxy, 4-hydroxy-2,2,6,6-tetramethyl-(2226-96-2)
EPA Substance Registry System1-Piperidinyloxy, 4-hydroxy-2,2,6,6-tetramethyl- (2226-96-2)
Safety Information
Hazard Codes Xn,Xi
Risk Statements 22-36/37/38-36/38
Safety Statements 26-36-37/39-36/37/39-27
WGK Germany 1
RTECS TN8991000
TSCA Yes
HS Code 29333999
Hazardous Substances Data2226-96-2(Hazardous Substances Data)
ToxicityLD50 oral in rat: 1053mg/kg
MSDS Information
ProviderLanguage
2,2,6,6-Tetramethyl freeagaoxy-4-piperidylEnglish
SigmaAldrichEnglish
ACROSEnglish
ALFAEnglish
4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy Usage And Synthesis
DescriptionTEMPOL is a piperidine nitroxide and spin label with superoxide dismutase (SOD) mimetic activity. It inhibits lipid peroxidation in rat liver microsomes with 50% inhibition of microsomal lipid peroxidation (IP50) values of 117, 61, and 381 μM for peroxidation induced by iron plus NADPH, iron plus ascorbate, and t-butylhydroperoxide, respectively. TEMPOL (1 mM) inhibits production of superoxide anions by 92% via a xanthine-xanthine oxidase reaction in vitro. It reduces mean arterial pressure and heart rate in spontaneously hypertensive rats (ED50s = 70 and 63 μmol/kg, respectively) when administered intravenously. TEMPOL is a cell-permeable spin label that has been used to quantify intracellular oxygen in various cell types by electron spin resonance (ESR) spectroscopy.
Chemical Propertiessolid
UsesA free radical scavenger
UsesSpin label for EPR studies; phase transfer dehydration catalyst; antioxidant; inhibitor of olefin free radical polymerization.
UsesTempol, a water-soluble piperidine nitroxide derivative having nonspecific radical-scavenging and superoxide dismutase (SOD) activity, protects cultured aerobic, but not hypoxic, cells against radiation-induced killing. Protection does not depend on intracellular thiols and does not involve O2-depletion. Tempol reacts with peroxyl radicals and can also oxidize DNA-bound metal ions, thereby interfering with OH? generation.
Synthesis Reference(s)Synthetic Communications, 19, p. 3509, 1989 DOI: 10.1080/00397918908052760
General Description4-Hydroxy-TEMPO is a 4-substituted 2,2,6,6-tetramethylpiperidyl-1-oxy (TEMPO) derivative. It is a low-molecular weight compound and has been proposed as superoxide dismutase mimic.
Flammability and ExplosibilityNonflammable
Biological ActivitySuperoxide scavenger that displays neuroprotective, anti-inflammatory and analgesic effects.
References1) Lipman et al. (2006), Neuroprotective effects if the stable nitroxide compound Tempol in 1-methyl-4-phenylpyridinium ion-induced neurotoxicity in the Nerve Growth Factor-differentiated model of pheochromocytoma PC12? cells; Eur. J. Pharmacol., 549 50 2) Guron et al. (2006), Acute effects of the superoxide dismutase mimetic tempol on split kidney function in two-kidney one-clip hypertensive rats; J. Hypertens., 24 387 3) Samuni and Barenholz (1997), Gamma-irradiation damage to liposomes differing in composition and their protection by nitroxides; Free Radic. Biol. Med., 23 972 4) Bernardy et al. (2017), Tempol, a Superoxide Dismutase Mimetic Agent, Inhibits Superoxide Anion-Induced Inflammatory Pain in Mice; Biomed. Res. Int., 2017 9584819 5) De Blasio et al. (2017), The superoxide dismutase mimetic tempol blunts diabetes-induced upregulation of NADPH oxidase and endoplasmic reticulum stress in a rat model of diabetic nephropathy; Eur. J. Pharmacol., 807 12
4-Hydroxy-2,2,6,6-tetramethyl-piperidinooxy Preparation Products And Raw materials
Preparation Products6-Hydroxy-2-naphthaldehyde

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