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Wichtige Dokumente
92688
5,5-Dimethyl-1-Pyrrolin N-Oxid
for ESR-spectroscopy
Synonym(e):
DMPO
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About This Item
Empirische Formel (Hill-System):
C6H11NO
CAS-Nummer:
Molekulargewicht:
113.16
Beilstein:
107603
EG-Nummer:
MDL-Nummer:
UNSPSC-Code:
12000000
PubChem Substanz-ID:
NACRES:
NA.21
Empfohlene Produkte
Qualität
for ESR-spectroscopy
Qualitätsniveau
Assay
≥98.0% (GC)
Form
crystals
Brechungsindex
n20/D 1.496 (lit.)
bp
75 °C/0.4 mmHg (lit.)
mp (Schmelzpunkt)
25-29 °C (lit.)
Dichte
1.015 g/mL at 25 °C (lit.)
Lagertemp.
−20°C
SMILES String
CC1(C)CCC=[N+]1[O-]
InChI
1S/C6H11NO/c1-6(2)4-3-5-7(6)8/h5H,3-4H2,1-2H3
InChIKey
VCUVETGKTILCLC-UHFFFAOYSA-N
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Anwendung
Neuroprotektives Mittel; Stickstoffmonoxid-Spin-Falle. Wird verwendet, um Radikale, die durch enzymatische Acetaldehyd-Oxidation gebildet werden, zu untersuchen.
Neuroprotektives Mittel; Stickstoffmonoxid-Spin-Falle. Wird verwendet, um Radikale, die durch enzymatische Acetaldehyd-Oxidation gebildet werden, zu untersuchen. Inkubation von Lymphozyten mit DMPO verringert DNA-Schäden durch NiCl2.
5,5-Dimethyl-1-pyrroline N-oxide is a reagent generally used either as a free-radical spin-trapping agent, or electrophilic component during the synthesis of pyrrolidine derivatives. It may also be considered as 1,3-dipole in cycloaddition processes.
Verpackung
Bottomless glass bottle. Contents are inside inserted fused cone.
Lagerklassenschlüssel
11 - Combustible Solids
WGK
WGK 3
Flammpunkt (°F)
203.0 °F - closed cup
Flammpunkt (°C)
95 °C - closed cup
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Karim Michail et al.
Analytical chemistry, 84(15), 6739-6746 (2012-06-26)
Free radicals are conventionally detected by electron paramagnetic resonance (EPR) spectroscopy after being trapped as spin adducts. Albeit this technique has demonstrated utmost efficacy in studying free radicals, its application to biological settings is intrinsically hampered by the inevitable bioreduction
Murugesan Velayutham et al.
Free radical biology & medicine, 51(1), 160-170 (2011-05-07)
In cells, mitochondria, endoplasmic reticulum, and peroxisomes are the major sources of reactive oxygen species (ROS) under physiological and pathophysiological conditions. Cytochrome c (cyt c) is known to participate in mitochondrial electron transport and has antioxidant and peroxidase activities. Under
Pedro L Zamora et al.
The journal of physical chemistry. A, 116(26), 7210-7218 (2012-06-07)
Radical forms of sulfur dioxide (SO(2)), sulfite (SO(3)(2-)), sulfate (SO(4)(2-)), and their conjugate acids are known to be generated in vivo through various chemical and biochemical pathways. Oxides of sulfur are environmentally pervasive compounds and are associated with a number
Emiko Sato et al.
Journal of biochemistry, 150(2), 173-181 (2011-05-17)
The nicotinamide adenine dinucleotide (NADH)/nicotinamide adenine dinucleotide phosphate (NADPH) oxidase and the xanthine oxidase (XOD) systems generate reactive oxygen species (ROS). In the present study, to characterize the difference between the two systems, the kinetics of ROS generated by both
Suchandra Bhattacharjee et al.
Nucleic acids research, 40(12), 5477-5486 (2012-03-06)
Oxidative stress-related damage to the DNA macromolecule produces lesions that are implicated in various diseases. To understand damage to DNA, it is important to study the free radical reactions causing the damage. Measurement of DNA damage has been a matter
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