The oxygen nonstoichiometry of SrFeO3−δ was determined by solid‐state Coulometric titration at 750°C‐1040°C and 10−18≤pO2(atm)≤0.5. At T≤850°C, a hysteresis in the oxygen nonstoichiometry (δ) isotherms indicates the presence of a two‐phase region corresponding to a mixture of a perovskite and an oxygen vacancy ordered phase. The variation of δ with temperature at fixed pO2 values and the variation of log(pO2) with reciprocal temperature at fixed δ are reported. The pO2 at the p‐n transition in the electrical conductivity increases as the temperature increases, and the transition in the conductivity isotherm occurs at a composition of SrFeO2.505(1) at 950°C and SrFeO2.508(1) at 900°C. Since strontium exclusively occupies the A‐site, a simple point defect model that assumes noninteracting defects can describe the isotherms but only at 1040°C; nonideal behavior is observed at lower temperatures. The partial molar thermodynamic quantities for oxygen in SrFeO3−δ were determined.