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244007

Sigma-Aldrich

3,3,5,5-Tetramethyl-1-pyrroline N-oxide

95%

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About This Item

Fórmula empírica (Notação de Hill):
C8H15NO
Número CAS:
Peso molecular:
141.21
Número MDL:
Código UNSPSC:
12352100
ID de substância PubChem:
NACRES:
NA.22

Ensaio

95%

Formulário

solid

p.e.

73 °C/1 mmHg (lit.)

pf

58-61 °C (lit.)

temperatura de armazenamento

−20°C

cadeia de caracteres SMILES

CC1(C)CC(C)(C)[N+]([O-])=C1

InChI

1S/C8H15NO/c1-7(2)5-8(3,4)9(10)6-7/h6H,5H2,1-4H3

chave InChI

GUQARRULARNYQZ-UHFFFAOYSA-N

Descrição geral

The ESR spectrum of 3,3,5,5-tetramethyl-1-pyrroline N-oxide was studied[1].

Aplicação

3,3,5,5-Tetramethyl-1-pyrroline N-oxide was used as a spin traping reagent[2].

Código de classe de armazenamento

11 - Combustible Solids

Classe de risco de água (WGK)

WGK 3

Ponto de fulgor (°F)

Not applicable

Ponto de fulgor (°C)

Not applicable

Equipamento de proteção individual

Eyeshields, Gloves, type N95 (US)


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D De Bono et al.
Free radical research, 20(5), 327-332 (1994-05-01)
The hydroxyl radical adducts of 5,5 dimethyl-1-pyrolline-N-oxide (DMPO) and 3,3,5,5 tetramethyl-1-pyrolline-N-oxide (TMPO) formed in the presence of hydrogen peroxide and FeII are normally quite stable, but in the presence of 5-20 micromolar myoglobin their ESR signals decay rapidly. This decay
E G Janzen et al.
Journal of biochemical and biophysical methods, 30(4), 239-247 (1995-11-01)
To obtain the strongest possible free radical spin adduct signal using the electron paramagnetic resonance spectroscopy-spin trapping technique, it is desirable to load an animal with the highest dose of spin trap possible. One hundred and twenty six male Sprague-Dawley
Shing-Jong Huang et al.
Solid state nuclear magnetic resonance, 29(4), 272-277 (2005-11-09)
We show that a Gaussian-shaped pulse can be used to excite selected 1H signals in hydroxyapatite, monetite and H-Y zeolite loaded with trimethylphosphine oxide (TMPO). This selective excitation method can be incorporated into Lee-Goldburg (LG) cross-polarization to obtain useful spectral
J F Torres-Roca et al.
Journal of immunology (Baltimore, Md. : 1950), 165(9), 4822-4830 (2000-10-25)
The roles of oxygen and reactive oxygen intermediates in apoptosis are unclear at present. Although oxygen and reactive oxygen intermediates are not required for the execution of apoptosis, oxygen may be involved in at least some forms of apoptosis. In
M J Davies et al.
The Biochemical journal, 240(3), 789-795 (1986-12-15)
Spin trapping using 5,5-dimethyl-1-pyrroline N-oxide (DMPO) has been used to detect and distinguish between the carbon-centred, alkoxyl, and peroxyl radicals produced during the photolytic decomposition of hydroperoxides. Photolysis of tert-butyl and cumene hydroperoxides, and peroxidized fatty acids, in toluene, with

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