We have studied crystallization remanent magnetization (CRM) in the γFe2O3 → αFe2O3 transformation, starting from synthetic, equidimensional maghemite crystals of single‐domain size (median diameter of 245 Å). Inversion of maghemite to hematite on heating was indicated by an exothermic peak in differential thermal analysis (DTA) at 555°C. In CRM experiments, samples of dispersed maghemite were heated in zero field to temperatures between 300°C and 604°C, held for 3 hours in a 50‐μT field HCRM, and cooled in zero field to 20°C. The intensity of the resulting CRM MCRM increased with increasing conversion to hematite, reaching a maximum of 784 A m−1 (0.784 emu cm−3) after the 556°C run, then decreased to 1.3 A m−1 (0.0013 emu cm−3) after the 604°C run. Maximum CRM intensity and the most rapid inversion indicated by DTA both occurred around 555°C. MCRM partially inverted samples was always parallel to HCRM. Hematite cannot explain the high intensity and moderate coercivity of the CRM. The bulk of the CRM seems to be carried by maghemite and to be acquired viscously rather than by grain growth. In a second set of experiments, CRM was produced in the presence of a preexisting anhysteretic remanent magnetization (ARM) MARM perpendicular to HCRM. The resulting remanence MT was a composite of surviving anhysteretic remanent magnetization ARM plus CRM directed parallel to HCRM, rather than a single vector of intermediate direction. MT can be synthesized by orthogonally combining CRMs measured in the first set of experiments with ARMs heated in zero field. Phase coupling of maghemite and hematite is not necessary to explain the main features of CRM, with or without an m initial remanence.