| Identification | Back Directory | [Name]
3-(AMINOMETHYL)-PROXYL | [CAS]
54606-49-4 | [Synonyms]
RARECHEM AL BW 2151
3-(AMINOMETHYL)-PROXYL
3-Aminomethyl-2,2,5,5-tetramethylpyrrolidine-N-oxy
3-Aminomethyl-2,2,5,5-tetramethylpyrrolidine-N-oxyl
3-AMINOMETHYL-2,2,5,5-TETRAMETHYL-1-PYRROLIDINYLOXY
3-aminomethyl-2,2,5,5-tetramethyl-1-pyrrolidinyl-n-oxyl
[3-(Aminomethyl)-2,2,5,5-tetramethylpyrrolizinooxy]radical
[4-(Aminomethyl)-2,2,5,5-tetramethylpyrrolizinooxy]radical
(3-Aminomethyl-2,2,5,5-tetramethyl-1-pyrrolidinyloxy)radical
[3-(Aminomethyl)-2,2,5,5-tetramethyl-1-pyrrolidinyloxy]radical | [Molecular Formula]
C9H19N2O * | [MDL Number]
MFCD00010547 | [MOL File]
54606-49-4.mol | [Molecular Weight]
171.26 |
| Chemical Properties | Back Directory | [Appearance]
Yellow-Orange Oil | [Boiling point ]
128-131 °C13 mm Hg(lit.)
| [Fp ]
144 °F
| [storage temp. ]
2-8°C | [solubility ]
Chloroform, Dichloromethane, Dimethyl Sulfoxide, Ethyl Acetate | [form ]
Oil | [color ]
Yellow-Orange |
| Hazard Information | Back Directory | [Chemical Properties]
Yellow-Orange Oil | [Uses]
Useful spin label for studying biological systems.
Used to study molecular diffusion into horse spleen ferritin and has been shown to be an effective nonthiol radioprotector.
Used in pharmacological studies of myeloperoxidase-mediated hypochlorous acid production inhibition
Reactant involved in:
- Reduction reactions with nitroxides
- Synthesis of adenosine methycarboxamides for use as cardioprotectants
| [Definition]
ChEBI: 3-(aminomethyl)-PROXYL is a member of aminoxyls, a member of pyrrolidines and a primary amine. It is functionally related to a PROXYL. |
|
| Company Name: |
Energy Chemical
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Sigma-Aldrich
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https://www.sigmaaldrich.cn |
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Medical Isotopes
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SIGMA-RBI
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