CAS 34322-45-7
:Pyridine-15N
Description:
Pyridine-15N is a nitrogen-labeled isotopic variant of pyridine, a heterocyclic aromatic organic compound characterized by a six-membered ring containing five carbon atoms and one nitrogen atom. The presence of the nitrogen-15 isotope, which is a stable isotope of nitrogen, allows for specific applications in nuclear magnetic resonance (NMR) spectroscopy and other analytical techniques, enhancing the study of molecular structures and dynamics. Pyridine itself is a colorless liquid with a distinctive, unpleasant odor, and it is known for its basicity and ability to act as a solvent and reagent in various chemical reactions. Pyridine-15N retains the chemical properties of pyridine while providing insights into nitrogen behavior in chemical environments. It is utilized in research and industrial applications, particularly in the fields of organic synthesis, pharmaceuticals, and materials science. Safety considerations include its flammability and potential health effects upon exposure, necessitating appropriate handling and storage measures.
Sort by
Purity (%)
0
100
|
0
|
50
|
90
|
95
|
100
Found 2 products.
Pyridine-15N
CAS:Controlled Product<p>Applications Pyridine-15N, is the labeled analogue of Pyridine (P991280), a basic six-membered heterocyclic ring. Pyridine is a base structure present in many biologically active compounds like the vitamins niacin and pyridoxal. Pyridine is used in dehalogenation reactions and can be used as a base in condensation reactions.<br>References Egyed, J. et al.: Bull. Soc. Chim. Fra., 11, 3014 (1973); Li, Y. et al.: Wuli HUa. Xueb., 14, 1048 (1998);<br></p>Formula:C5H515NColor and Shape:NeatMolecular weight:80.09Pyridine-15N
CAS:Controlled Product<p>Pyridine-15N is a chemical compound that has been shown to be a promising candidate for molecular hydrogen storage. It is believed that the pyridine ring of Pyridine-15N interacts with the proton, forming a pyridinium ion. This interaction may be due to the increased temperatures and simulations used in this study, as well as the magnetic resonance spectroscopy techniques. The reaction selectivity of Pyridine-15N was found to depend on its acid moieties and the mesoporous nature of silicon. The hydrogen bond between these two compounds also contributed to its stability and reactivity.</p>Formula:C5H5NPurity:Min. 95%Molecular weight:79.1 g/mol

