Paria, Santanu et al. published their research in Industrial & Engineering Chemistry Research in 2006 | CAS: 104-73-4

1-Dodecylpyridin-1-ium bromide (cas: 104-73-4) belongs to pyridine derivatives. In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. Halopyridines are particularly attractive synthetic building blocks in a variety of cross-coupling methods, including the Suzuki-Miyaura cross-coupling reaction.Application of 104-73-4

Effects of Chain Length and Electrolyte on the Adsorption of n-Alkylpyridinium Bromide Surfactants at Sand-Water Interfaces was written by Paria, Santanu;Yuet, Pak K.. And the article was included in Industrial & Engineering Chemistry Research in 2006.Application of 104-73-4 This article mentions the following:

The kinetic and equilibrium studies of the adsorption of four cationic surfactants (pyridinium bromide) with different chain lengths (C16, C14, C12, and C10) onto sand are presented here. The adsorption and desorption behavior in the absence and presence of different electrolytes (NaCl, CaCl2, and Na2SO4) are compared in batch and continuous column experiments The kinetic studies show that the rates of adsorption of pyridinium bromide surfactants on sand surfaces are very high (閳?0% of saturation adsorption occurs in 30 s) and are almost the same at low concentration (0.5 mM) for different chain lengths. The amount of surfactant adsorbed is enhanced by the presence of electrolyte because of a reduction in electrostatic repulsion among the headgroups, whereas the effect of the valence of coion does not appear to be important. Desorption studies based on column experiments show that a lower amount of surfactant is retained when eluted with electrolyte solution instead of pure water. In the experiment, the researchers used many compounds, for example, 1-Dodecylpyridin-1-ium bromide (cas: 104-73-4Application of 104-73-4).

1-Dodecylpyridin-1-ium bromide (cas: 104-73-4) belongs to pyridine derivatives. In contrast to benzene, Pyridine’s electron density is not evenly distributed over the ring, reflecting the negative inductive effect of the nitrogen atom. Halopyridines are particularly attractive synthetic building blocks in a variety of cross-coupling methods, including the Suzuki-Miyaura cross-coupling reaction.Application of 104-73-4

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem