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Merck

80126

Supelco

N-tert-Butyl-α-phenylnitrone

for ESR-spectroscopy

Sinónimos:

N-Benzylidene-tert-butylamine N-oxide, PBN, Phenyl N-t-butylnitrone

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About This Item

Fórmula lineal:
C6H5CH=N(O)C(CH3)3
Número de CAS:
Peso molecular:
177.24
Beilstein:
2044028
Número CE:
Número MDL:
Código UNSPSC:
12000000
ID de la sustancia en PubChem:
NACRES:
NA.21

grado

for ESR-spectroscopy

Nivel de calidad

Análisis

≥99.5% (HPLC)

formulario

powder

mp

72-74 °C
73-74 °C (lit.)

solubilidad

chloroform: 50 mg/mL, clear, colorless

temp. de almacenamiento

−20°C

cadena SMILES

CC(C)(C)[N+](\[O-])=C\c1ccccc1

InChI

1S/C11H15NO/c1-11(2,3)12(13)9-10-7-5-4-6-8-10/h4-9H,1-3H3/b12-9-

Clave InChI

IYSYLWYGCWTJSG-XFXZXTDPSA-N

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Aplicación

N-tert-Butyl-a-phenylnitrone was used as spin trapping agent during measurement of scavenging rate constant of carotenoid using EPR spin-trapping technique. This reagent helps in obtaining a six-line ESR spectrum and hyperfine coupling constants, confirming the presence of carbon-based radical in uric acid and peroxynitrite, using electron spin resonance spectroscopy and liquid chromatography mass spectrometry.

Acciones bioquímicas o fisiológicas

N-tert-butyl-α-phenylnitrone (PBN) is a commonly used free-radical spin trap. It has been shown to reduce the number of emboli-induced cerebral microinfarctions in the rabbit cortex and prevent neoplasia by its radical scavenging activity and its ability to inhibit cyclooxygenase-2 activity. Reported to inhibit the induction of nitric oxide synthase (iNOS), thereby preventing the overproduction of nitric oxide (NO). PBN in a dose of 100 mg/kg i.p. reduced necrosis of the substantia nigra, pars reticulate in flurothyl-induced status epilepticus in rats. It protects against some types of post-trauma epileptogenic events in an animal model of epilepsy. The lethal dose of PBN in rats was found to be approximately 100 mg/100 g body weight (0.564 mmol/100Å g).

Código de clase de almacenamiento

11 - Combustible Solids

Clase de riesgo para el agua (WGK)

WGK 3

Punto de inflamabilidad (°F)

Not applicable

Punto de inflamabilidad (°C)

Not applicable


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Antioxidant and redox properties of supramolecular complexes of carotenoids with beta-glycyrrhizic acid.
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