The objective of this research was to test an appropriate DNA barcode from four candidate barcoding loci (matK, rbcL, psbA-trnH and ITS2) for discrimination between Illicium verumand its congeneric toxic adulterants in trade. Twenty fresh samples from 8 species of the genera Illicium were collected from four areas of China, and two samples of medicinal material of I. verum were purchased respectively, from the market and pharmacy. In this study, PCR amplification success rate, sequencing efficiency, the intra- and inter-specific divergences, and DNA barcoding gap were employed to assess the ability of each barcode for the authentication of I. verum and its adultrants. The results showed that psbA-trnHexhibited the highest inter-specific divergence among the four DNA barcoding sequences and the highest species identification efficiency at 100% both by BLAST1 and the nearest distance method. In addition, the psbA-trnH query sequences of the two dried fruits were compared with the reference sequence by BLAST1, they were identified as I. verum. Our findings supported the notion that the psbA-trnH region could distinguish I. verum from other adulterating species. Key words: Illicium verum, psbA-trnH, identification, DNA barcoding, Illiciaceae, medicinal material.