Reference of 6645-46-1, Redox catalysis has been broadly utilized in electrochemical synthesis due to its kinetic advantages over direct electrolysis. The appropriate choice of redox mediator can avoid electrode passivation and overpotential. 6645-46-1, Name is (R)-3-Carboxy-2-hydroxy-N,N,N-trimethylpropan-1-aminium chloride, SMILES is C[N+](C)(C)C[C@H](O)CC(O)=O.[Cl-], belongs to chiral-catalyst compound. In a article, author is Zhang Wei-Min, introduce new discover of the category.
The effect of the nonionic surfactant primary alcobol ethoxylate (AEO-3) as an additive on the crystallization of beta zeolites was investigated by adding it into the conventional hydrothermal synthesis system of the beta zeolites with a formula of n(Al2O3):n(SiO2):n(Na2O):n(TEAOH):n(H2O):n(AEO-3):n(C2H5OH)=(0.28 similar to 1):40:1.55:10:640:(0.45 similar to 7.69):11.37. It was indicated that the addition of AEO-3 could promote the formation of aluminosilicate sol and increase the degree of its homogenization, as well as the yield of the product. The as-synthesized samples were characterized by X-ray diffraction, N-2 and Ar adsorption-desorption, scanning electron microscope, NMR and n-decane adsorption. The results showed that the nano particles of beta zeolites were more complete and uniform, the crystallinity and micropore volume increased by the addition of surfactant AEO-3, and the yield of product, Si/Al ratio and acid strength increased as well. In addition, the addition of AEO-3 increased the proportion of chiral polymorph A in the structure of beta zeolites.
Reference of 6645-46-1, The reactant in an enzyme-catalyzed reaction is called a substrate. Enzyme inhibitors cause a decrease in the reaction rate of an enzyme-catalyzed reaction.I hope my blog about 6645-46-1 is helpful to your research.
Reference:
Chiral Catalysts,
,Chiral catalysts – SlideShare