Discovery of 2213-43-6

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Application of 2213-43-6, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 2213-43-6

Application of 2213-43-6, The reaction rate of a catalyzed reaction is faster than the reaction rate of the uncatalyzed reaction at the same temperature.2213-43-6, Name is 1-Aminopiperidine, molecular formula is C5H12N2. In a Article,once mentioned of 2213-43-6

N-aminopiperidine (NAPP) belongs to a large family of compounds, namely the cyclic alkylhydrazines, used as precursors for different targets in fine chemicals, such as pharmaceuticals and cosmetics. The formation of NAPP via the Raschig process by reacting piperidine (C5H10NH, PP) with monochloramine (NH2Cl) involves many side-reactions because of the reactivity of the latter. An exhaustive kinetic model, which reflects the rate of NAPP formation and that of side-reactions occurring during the synthesis of NAPP, was established. Additionally, a comparative study of theoretical and experimental concentration-time curves permitted to verify the accuracy of the model in a diluted medium. Moreover, the established kinetic model allowed to define the optimal conditions for NAPP synthesis in a concentrated medium, by varying the reactants concentrations, [PP]/[NH2Cl] ratio, pH and temperature. Hence, the application of the kinetic model enabled to optimize the reaction in view of its transfer to a continuous process.

One of the oldest and most widely used commercial enzyme inhibitors is aspirin, Application of 2213-43-6, which selectively inhibits one of the enzymes involved in the synthesis of molecules that trigger inflammation. you can also check out more blogs about 2213-43-6

Reference:
Piperidine – Wikipedia,
Piperidine | C5H915N – PubChem