14691-88-4
Chemical Structure
4-Amino-TEMPO
Synonym(s): 4-Amino-2,2,6,6-tetramethylpiperidine-1-oxyl
- CAS No.: 14691-88-4
- Formula:C9H19N2O
- Molecular Weight:171.26
InChIKey: XUXUHDYTLNCYQQ-UHFFFAOYSA-N
SMILES: CC1(C)N([O])C(C)(C)CC(N)C1
Biological Activity: 4-Amino-TEMPO (4-Amino-2,2,6,6-tetramethylpiperidine-1-oxyl) is a stable nitroxide radical and N-nucleophile based on TEMPO. 4-Amino-TEMPO has superoxide dismutase-mimetic activity, can protect cells from oxidative damage, and has radioprotective effects. 4-Amino-TEMPO is widely used in fields such as biomedicine, materials science, and industrial production. 4-Amino-TEMPO can be used as a spin label to detect free radicals, an oxidation catalyst in industrial production, and an antioxidant stabilizer for polymers, among others[1][2].
| Cat. No. | Product Name | Purity | Description | Pricing | |||||||||||||||||||
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4-Amino-TEMPO | 99.84% | 4-Amino-TEMPO (4-Amino-2,2,6,6-tetramethylpiperidine-1-oxyl) is a stable nitroxide radical and N-nucleophile based on TEMPO. 4-Amino-TEMPO has superoxide dismutase-mimetic activity, can protect cells from oxidative damage, and has radioprotective effects. 4-Amino-TEMPO is widely used in fields such as biomedicine, materials science, and industrial production. 4-Amino-TEMPO can be used as a spin label to detect free radicals, an oxidation catalyst in industrial production, and an antioxidant stabilizer for polymers, among others. | ||||||||||||||||||||
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4-Amino-TEMPO-d17 | 4-Amino-TEMPO-d17 (4-Amino-2,2,6,6-tetramethylpiperidine-1-oxyl-d17) is the deuterium labeled 4-Amino-TEMPO (HY-W002004). 4-Amino-TEMPO (4-Amino-2,2,6,6-tetramethylpiperidine-1-oxyl) is a stable nitroxide radical and N-nucleophile based on TEMPO. 4-Amino-TEMPO has superoxide dismutase-mimetic activity, can protect cells from oxidative damage, and has radioprotective effects. 4-Amino-TEMPO is widely used in fields such as biomedicine, materials science, and industrial production. 4-Amino-TEMPO can be used as a spin label to detect free radicals, an oxidation catalyst in industrial production, and an antioxidant stabilizer for polymers, among others. | |||||||||||||||||||||
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4-Amino-TEMPO-d17,15N | 4-Amino-TEMPO-d17,15N (4-Amino-2,2,6,6-tetramethylpiperidine-1-oxyl-d17,15N) is the deuterium labeled 4-Amino-TEMPO-d17 (HY-W002004S1). 4-Amino-TEMPO (4-Amino-2,2,6,6-tetramethylpiperidine-1-oxyl) is a stable nitroxide radical and N-nucleophile based on TEMPO. 4-Amino-TEMPO has superoxide dismutase-mimetic activity, can protect cells from oxidative damage, and has radioprotective effects. 4-Amino-TEMPO is widely used in fields such as biomedicine, materials science, and industrial production. 4-Amino-TEMPO can be used as a spin label to detect free radicals, an oxidation catalyst in industrial production, and an antioxidant stabilizer for polymers, among others. | |||||||||||||||||||||
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Similarity Score 0.90
HY-100561RTempol (Standard) -
Similarity Score 0.83
HY-W001187Tempo -
Similarity Score 0.82
HY-W7770724-Isocyanato-TEMPO,Technical grade -
Similarity Score 0.82
HY-151847N3-TEMPO -
Similarity Score 0.82
HY-129242Tempone -
Similarity Score 0.78
HY-23033Tempone-H -
Similarity Score 0.75
HY-Y17542,2,6,6-Tetramethylpiperidine-N-oxyl-4-amino-4-carboxylic acid -
Similarity Score 0.75
HY-B1382APempidine hydrochloride -
Similarity Score 0.75
HY-B1382Pempidine -
Explore the MedChemAI to find more analogs
References
- [1]. Żamojć K, Zdrowowicz M, Hać A, et al. Dihydroxy-substituted coumarins as fluorescent probes for nanomolar-level detection of the 4-amino-TEMPO spin label[J]. International journal of molecular sciences, 2019, 20(15): 3802. [Content Brief]
- [2]. Gergely M, et al. 4‐Amino‐TEMPO as N‐Nucleophile in Palladium‐Catalyzed Aminocarbonylation. Journal of Heterocyclic Chemistry, 2017, 54(1): 634-640.
