Abstract
The HPTLC behavior of closely related N-phenylamide derivatives of phenoxyacetic acid has been studied on silica gel and diol-modified silica gel layers developed with binary non-aqueous mobile phases (ethyl acetate, dioxane, or methyl ethyl ketone in n-heptane or dichloromethane). The influence of the different polar modifiers on the retention was illustrated as linear plots of RM = f(log c). The separation selectivities of the investigated compounds on silica gel and diol phases were compared as RM(silica) vs. RM(diol) relationships.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
