所有图片(3)
别名:
4-氨基-2,2,6,6-四甲基哌啶-1-氧, 4-氨基-2,2,6,6-四甲基哌啶氧自由基, 4-氨基-TEMPO
经验公式（希尔记法）:
C9H19N2O
CAS号:
分子量:
171.26
Beilstein:
3933966
EC 号:
MDL编号:
UNSPSC代码:
12352000
PubChem化学物质编号:
NACRES:
NA.22
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应用
可用于研究生物系统、聚合物的自旋标记物，并且可作为更复杂的自旋标记物的结构单元。
警示用语：
Warning
危险声明
危险分类
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
靶器官
Respiratory system
WGK
WGK 3
个人防护装备
dust mask type N95 (US), Eyeshields, Gloves
N Naber et al.
Biochemistry, 33(13), 3855-3861 (1994-04-05)
Each actin molecule contains a nucleotide, tightly bound in a deep cleft that divides the molecule. To probe conformational changes within this region of the molecule, we have incorporated two spin label analogues of ATP into actin. In both analogs
Spin-Labeled Dendrimers in EPR Imaging with Low Molecular Weight Nitroxides.
Alexander T. Yordanov et al.
Angewandte Chemie (International ed. in English), 40(14), 2690-2692 (2001-07-18)
D A Hall et al.
Science (New York, N.Y.), 276(5314), 930-932 (1997-05-09)
Large dynamic nuclear polarization signal enhancements (up to a factor of 100) were obtained in the solid-state magic-angle spinning nuclear magnetic resonance (NMR) spectra of arginine and the protein T4 lysozyme in frozen glycerol-water solutions with the use of dynamic
Jianfei Jiang et al.
The Journal of pharmacology and experimental therapeutics, 320(3), 1050-1060 (2006-12-21)
Suppression of mitochondrial production of reactive oxygen species is a promising strategy against intrinsic apoptosis typical of degenerative diseases. Stable nitroxide radicals such as 4-hydroxy-2,2,6,6-tetramethyl piperidine-1-oxyl (TEMPOL) and its analogs combine several important features, including recycleability, electron acceptance from respiratory
Tareq Taha Jubeh et al.
Molecular pharmaceutics, 2(1), 2-11 (2005-04-05)
The purpose of the present study was to investigate whether the local prevention of luminal superoxide-mediated biological damage in the rat jejunal mucosa could be achieved by liposomal superoxide dismutase (SOD) and the SOD mimic tempamine (TMN). Cationic liposomes loaded
商品
TEMPO（2,2,6,6-四甲基哌啶氧基或2,2,6,6-四甲基哌啶1-氧基）及其衍生物在有机氧化反应催化剂中可以作为稳定的硝酰基使用。TEMPO由Lebedev和Kazarnovskii于1960年发现，其具有的稳定自由基性质得益于其庞大的取代基团阻碍了自由基与其他分子之间发生反应。
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