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Chiral separation of rac ‐Ornidazole and detection of the impurity of ( R )‐Ornidazole in ( S )‐Ornidazole injection and raw material
Author(s) -
Huang Jianquan,
Cao Guoying,
Hu Xin,
Sun Chunhua,
Zhang Junren
Publication year - 2006
Publication title -
chirality
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.43
H-Index - 77
eISSN - 1520-636X
pISSN - 0899-0042
DOI - 10.1002/chir.20292
Subject(s) - ornidazole , chemistry , chromatography , isopropyl alcohol , hexane , methanol , enantiomer , impurity , chirality (physics) , resolution (logic) , high performance liquid chromatography , isopropyl , acetonitrile , organic chemistry , chiral symmetry breaking , physics , quantum mechanics , artificial intelligence , computer science , nambu–jona lasinio model , quark
( S )‐Ornidazole is a subject of research as an antifertility agent in male animals at present. However, there seems to be no relative report on chiral separation for rac ‐Ornidazole, which has been used as an effective medicine for more than 30 years. In this article, the chiral separation of rac ‐Ornidazole on a Chiralcel OB‐H column based on normal‐phase high‐performance liquid chromatography (NP‐HPLC) is investigated and the methodology for detection of impurity of ( R )‐Ornidazole in ( S )‐Ornidazole injection and raw material is established. The novel mobile phase is utilized by mixing n ‐hexane, methanol and isopropyl alcohol (95:4:1, v/v/v) instead of the typical mobile phase of n ‐hexane and isopropyl alcohol, although the methanol, which offers a good resolution factor for the enantiomeric separation in this system, is not recommended on the Chiralcel OB‐H column according to the instruction supplied by Daicel Chemical Ind., LTD (Japan). Chirality, 2006. © 2006 Wiley‐Liss, Inc.