Abstract3‐Deoxyanthocyanidins (3‐DAS) are the unique flavonoid compounds in sorghum. The majority of research to date have concentrated on the biological activity and extraction of 3‐DAS from sorghum and lacked systematic purification and identification investigations. Herein, a facile method for the purification of sorghum 3‐DAS from the acidic methanol solution crude extract using macroporous resins (MARs) was proposed and investigated in this work. Based on the experimental data, commercial MAR AB‐8 was selected to achieve the purification of sorghum 3‐DAS. The adsorption‐desorption experiment confirmed the optimal procedure. With this procedure, the total purity of 3‐DAS was 19.32%, and 3‐DAS content in the purified product was 8.4 times higher than that in the crude extract. UPLC‐QTRAP‐MS/MS identification indicated that the purified 3‐DAS product was mainly composed of apigeninidin, luteolinidin, and their methoxy derivatives. Besides, the purified product exhibited better bioactivities than the crude extract, including the scavenging activities for DPPH, ABTS+, and hydroxyl radicals, the total antioxidant capacity, and the inhibitory effects for α‐amylase, α‐glucosidase, and lipase. This work provides a potential way for the large‐scale purification of bioactive sorghum 3‐DAS from crude extract, which is significant to deepen the applications of sorghum 3‐DAS in the food nutrition and pharmaceutical industries.