Crystal violet (CV) dye has been used in the textile industry, as printing ink, biological stain, and antimicrobial agent. CV dye persists in water for a long time and poses a serious threat to humans and aquatic life. In this study, g‐C3N4, MnFe2O4 nanoparticles, and g‐C3N4@MnFe2O4 (80 : 20 wt %) nanocomposite were synthesized via thermal decomposition and chemical co‐precipitation routes. The crystallite size was found 36.31 nm and 30 nm for bare MnFe2O4 nanoparticle and g‐C3N4@MnFe2O4 nanocomposite respectively. The optical band gaps of MnFe2O4, g‐C3N4, and g‐C3N4@MnFe2O4 were 1.8 eV, 2.7 eV, and 2.4 eV, respectively. The photoluminescence intensity decreases in the following order: g‐C3N4>g‐C3N4@MnFe2O4 nanocomposite>MnFe2O4. The degradation efficiency of MnFe2O4, g‐C3N4, and g‐C3N4@MnFe2O4 nanocomposite was found to be 25.13 %, 58.11 %, and 98.42 % respectively, and followed first‐order kinetics. The value of the rate constant for g‐C3N4@MnFe2O4 was 0.022 min−1 which was around ten times higher than g‐C3N4 and MnFe2O4. By adding three scavengers, the degradation capacity of nanocomposite was decreased in the order AA (L‐ascorbic acid)>EDTA (ethylenediaminetetraacetic acid)>TBA (t‐butyl alcohol). A slight reduction in degradation efficiency was observed after five consecutive cycles. Thus, this new finding can be applied to the degradation of CV dye‐contaminated industrial wastewater under solar light.