We make derivatives of (iso)nicotinamides. In some cases the C-13 linewidths are broader for carbon atoms directly attached to the pyridine nitrogen, but sometimes not. There might be a relationship with whether or not the pyridine nitrogen is alkylated. I seem to recall reading about this many years ago and thinking that it was in some way related to the fact that N-14 is quadrupolar, but I cannot recall the details. Does anyone have any thoughts?