244007
3,3,5,5-Tetramethyl-1-pyrroline N-oxide
95%
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About This Item
Formula empirica (notazione di Hill):
C8H15NO
Numero CAS:
Peso molecolare:
141.21
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Saggio
95%
Stato
solid
P. ebollizione
73 °C/1 mmHg (lit.)
Punto di fusione
58-61 °C (lit.)
Temperatura di conservazione
−20°C
Stringa SMILE
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
GUQARRULARNYQZ-UHFFFAOYSA-N
Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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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
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
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
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
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