51526-59-1

Basic information

• Product Name: 1-oxyl-2,2,6,6-tetramethyl-4-piperidyl-N,N,N',N'-bis(ethylene)phosphorodiamidothioate
• Synonyms: 1-oxyl-2,2,6,6-tetramethyl-4-piperidyl-N,N,N',N'-bis(ethylene)phosphorodiamidothioate
• CAS NO: 51526-59-1
• Molecular Formula: C13H25N3O2PS *
• Molecular Weight: 318.395261
• Mol File: 51526-59-1.mol
• Article Data: 2

Chemical Properties

• Boiling Point: 403.8°Cat760mmHg
• Flash Point: 198°C
• Appearance: /
• Density: 1.3g/cm³
• CAS DataBase Reference: 1-oxyl-2,2,6,6-tetramethyl-4-piperidyl-N,N,N',N'-bis(ethylene)phosphorodiamidothioate(CAS DataBase Reference)
• NIST Chemistry Reference: 1-oxyl-2,2,6,6-tetramethyl-4-piperidyl-N,N,N',N'-bis(ethylene)phosphorodiamidothioate(51526-59-1)
• EPA Substance Registry System: 1-oxyl-2,2,6,6-tetramethyl-4-piperidyl-N,N,N',N'-bis(ethylene)phosphorodiamidothioate(51526-59-1)

Safety Data

• Hazardous Substances Data: 51526-59-1(Hazardous Substances Data)

Usage

Chemical Structure

1-oxyl-2,2,6,6-tetramethyl-4-piperidyl-N,N,N',N'-bis(ethylene)phosphorodiamidothioate

Explanation

TEMPOL is a nitroxide free radical compound with a complex structure that includes a 4-piperidine ring, a phosphorodiamidothioate group, and an ethylene group.

Explanation

TEMPOL is a stable free radical, meaning it does not readily undergo reactions that would alter its structure or properties.

Explanation

TEMPOL's unique properties make it an ideal spin-labeling agent for studying the behavior of molecules in various chemical and biological systems.

Explanation

TEMPOL can neutralize reactive oxygen species, which are harmful molecules that can cause cellular damage and contribute to various diseases.

Explanation

TEMPOL can protect cells from oxidative damage by neutralizing reactive oxygen species and other harmful molecules.

Explanation

TEMPOL has been shown to have various therapeutic effects, including reducing inflammation, inhibiting tumor growth, and protecting neurons from damage.

Explanation

Due to its various therapeutic effects, TEMPOL has potential applications in the treatment of cardiovascular diseases and as a contrast agent in imaging techniques to improve the visualization of biological structures.

Explanation

The IUPAC name is the official chemical name for TEMPOL, which provides a detailed description of its structure and composition.

Stability

Stable nitroxide free radical

Spin-labeling agent

Widely used in chemical and biological research

Reactive oxygen species scavenger

Ability to scavenge reactive oxygen species

Antioxidant properties

Acts as an antioxidant

Therapeutic effects

Anti-inflammatory, antitumor, and neuroprotective properties

Potential applications

Treatment of cardiovascular diseases and as a contrast agent in imaging techniques

InChI:InChI=1/C13H25N3O2PS/c1-12(2)9-11(10-13(3,4)16(12)17)18-19(20,14-5-6-14)15-7-8-15/h11H,5-10H2,1-4H3

Downstream Products

• 78996-69-7 1-hydroxy-2,2,6,6-tetramethyl-4-piperidyl N,N:N',N'-phosphorodiamidothioate 

Relevant articles and documents

Improvements in the preparation of spin labeled phosphorus compounds of potential cytotoxicity

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