Hydroxylamine (NH2OH or HA) is a redox-active nitrogen oxide that occurs as a toxic intermediate in the oxidation of ammonium by nitrifying and methanotrophic bacteria. Within ammonium containing environments, HA is generated by ammonia monooxygenase (nitrifiers) or methane monooxygenase (methanotrophs). Subsequent oxidation of HA is catalyzed by heme proteins, including cytochromes P460 and multiheme hydroxylamine oxidoreductases, the former contributing to emissions of N2O, an ozone-depleting greenhouse gas. A heme-HA complex is also a proposed intermediate in the reduction of nitrite to ammonia by cytochrome c nitrite reductase. Despite the importance of heme-HA complexes within the biogeochemical nitrogen cycle, fundamental aspects of their coordination chemistry remain unknown, including the effect of the Fe redox state on heme-HA affinity, kinetics, and spectroscopy. Using stopped-flow UV-vis and resonance Raman spectroscopy, we investigated HA complexes of the L16G distal pocket variant of Alcaligenes xylosoxidans cytochrome c'-alpha (L16G AxCP-alpha), a pentacoordinate c-type cytochrome that we show binds HA in its Fe(III) (K-d similar to 2.5 mM) and Fe(II) (K-d = 0.0345 mM) states. The similar to 70-fold higher HA affinity of the Fe(II) state is due mostly to its lower k(off) value (0.0994 s(-1) vs 11 s(-1)), whereas k(on) values for Fe(II) (2880 M-1 s(-1)) and Fe(III) (4300 M-1 s(-1)) redox states are relatively similar. A comparison of the HA and imidazole affinities of L16G AxCP-alpha was also used to predict the influence of Fe redox state on HA binding to other proteins. Although HA complexes of L16G AxCP-alpha decompose via redox reactions, the lifetime of the Fe(II)HA complex was prolonged in the presence of excess reductant. Spectroscopic parameters determined for the Fe(II)HA complex include the N-O stretching vibration of the NH2OH ligand, nu(N-O) = 906 cm(-1). Overall, the kinetic trends and spectroscopic benchmarks from this study provide a foundation for future investigations of heme-HA reaction mechanisms.