This article establishes the processing-microstructure-motion-property relationship of high-speed melt-spun nylon-6 fibers. From solid-state H-1 NMR T-1 rho (spin-lattice relaxation time in the rotating frame) relaxation studies, all nylon-6 fibers spun at 4500-6100 m/min showed three-component exponential decay with the time constants T-1 rho ,T-I, T-1 rho ,T-II, and T-1 rho ,T-III, indicating that there existed three different motional phases. These phases were assigned to immobile crystalline, intermediate rigid amorphous, and mobile amorphous regions. The determination of the correlation time (tau (c)) of the respective phases provided information about the local molecular mobility of each phase with respect to the spinning speed. As the spinning speed increased, tau (c) of the crystalline region increased (4500-5200 m/min) and then reached a plateau. However, tau (c) for the rigid amorphous region increased from 5200 m/min onward, indicating that the rigid amorphous chains were more oriented and constrained in the spinning speed range of 5500-6100 m/min. The drastic increase of the maximum thermal stress for all fibers from 5500 to 6100 m/min was coincident with the tau (c) characteristics of the rigid amorphous region. The significant increase in tenacity and Young's modulus and the large decrease in elongation at break at 5500-6100 m/min were also in good agreement with the local molecular motion of the intermediate rigid amorphous phase in the nylon-6 fibers.