| 1995 | Folia Pharm. Univ. Carol. 19 | Pag. 57—62 |
Jiří Gabriel1, Naďa Zimová2, Ivan Němec2, Karel Waisser3 (waisser@faf.cuni.cz), Alexandr Hrabálek3
1Microbiological Institute, Academy of Sciences of the Czech Republic, Prague
2Department of Analytical Chemistry, Faculty of Natural Science, Charles University, Prague, Czech Republic
3Department of Inorganic and Organic Chemistry, Faculty of Pharmacy, Charles University, Hradec Králové, Czech Republic
The basic chromatographic study of a new 1-phenyl-5-mercaptotetrazole derivatives was performed using a silica column with chloroform—acetonitrile (containing 1% of acetic acid) mobile phase. The optimal composition of mobile phase for 1-(4-bromophenyl)-5-mercaptotetrazole, compound with the best thyreostatic activity from other derivatives, was chloroform : acetonitrile 92.5 : 7.5. The detection limit of 1-(4-bromophenyl)-5-mercaptotetrazole, 2 ng (injection 1 µl), was established.