2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na

2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na Suppliers list
Company Name: Merck KGaA  
Tel: 21-20338288
Email: ordercn@merckgroup.com
Company Name: Santa Cruz Biotechnology Inc  
Tel: 021-60936350
Email: scbt@scbt.com
Company Name: Absin Bioscience Inc.  
Tel: 021-38015121-8802
Email: chenjw@absin.cn
Company Name: EMD Biosciences, Inc.  
Tel: 858 450 5500
Email: technical@calbiochem.com
2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na Basic information
Product Name:2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na
Synonyms:CARBOXY-PTIO, SODIUM SALT;2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na
CAS:
MF:C14H16N2NaO4*
MW:299.28
EINECS:
Product Categories:
Mol File:Mol File
2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na Structure
2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na Chemical Properties
storage temp. -20°C
solubility HEPES Buffer: 0.4mg/mL
form solid
color dark blue
Safety Information
WGK Germany WGK 1
Storage Class11 - Combustible Solids
MSDS Information
2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na Usage And Synthesis
UsesReacts with nitric oxide at pH 7.4, resulting in the generation of NO2-/NO3- with a rate constant of 1 x 104 M-1sec-1. Prevents SIN-1 induced endothelial cell death. Reported to have potent therapeutic value in endotoxin shock through its nitric oxide scavenging action.
Biological ActivityCell permeable: no', 'Primary Target
Nitric oxide scavenging action', 'Product does not compete with ATP.', 'Reversible: no
2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na Preparation Products And Raw materials
Tag:2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide, na Related Product Information
Carboxy-ptio 2-(4-Carboxyphenyl)-4,4,5,5-tetramethylimidazoline-1-oxyl-3-oxide CARBOXY-PTIO