High-performance liquid chromatography factor

B. Waiczak, L. Morin-Allory, M. Chrdtien, M. Lafosse and M. Dreux, Factor analysis and experiment design in high-performance liquid chromatography. III. Influence of mobile phase modifications on the selectivity of chalcones on a diol stationary phase. Chemom. Intell. Lab. Syst., I (1986) 79-90. 

Guo, D., Mant, C. T., Taneja, A. K., and Hodges, R. S., Prediction of peptide retention times in reversed-phase high-performance liquid chromatography II. Correlation of observed and predicted petide retention times and factors influencing the retention times of peptides, /. Chromatogr., 359, 519,1986. 

Dong, M.W., Tran, A.D. (1990). Factors influencing the performance of peptide mapping by reversed-phase high-performance liquid chromatography. J. Chromatogr. 499, 125-139. 

Enantiomers of the 8,9-dichloro-2,3,4,4 ,5,6-hexahydro-177-pyrazino[l,2-tf]quinoxalin-5-one (structure 249 Rz = R3 = Cl R1 = R4 = H) could be separated by normal-phase, chiral high-performance liquid chromatography (HPLC) with increased retention and separation factors if ethoxynonafluorobutane was used as solvent, instead of -hexane <2001JCH(918)293>. 

Aboul-Enein and Ali [78] compared the chiral resolution of miconazole and two other azole compounds by high performance liquid chromatography using normal-phase amylose chiral stationary phases. The resolution of the enantiomers of ( )-econazole, ( )-miconazole, and (i)-sulconazole was achieved on different normal-phase chiral amylose columns, Chiralpak AD, AS, and AR. The mobile phase used was hexane-isopropanol-diethylamine (400 99 1). The flow rates of the mobile phase used were 0.50 and 1 mL/min. The separation factor (a) values for the resolved enantiomers of econazole, miconazole, and sulconazole in the chiral phases were in the range 1.63-1.04 the resolution factors Rs values varied from 5.68 to 0.32. 

Sherblom, P.M., Eganhouse, R.P. (1988) Correlations between octanol-water partition coefficients and reversed-phase high-performance liquid chromatography capacity factors. J. Chromtogr. 454, 37-50. 

Hamisch, M., Mockel, H.J., Schule, G. (1983) Relationship between log Pow shake-flask values and capacity factors derived from reversed-phase high-performance liquid chromatography for n-alkylbenzenes and some OECD reference substances. J. Chromatogr. 282, 315-332. 

Vowles and Mantoura [38] determined sediment-water partition coefficients and the high-performance liquid chromatography capacity factors for 14 alkylbenzene and polyaromatic hydrocarbons. The partition coefficients correlated well with the alkyl-cyano capacity factors, and it was concluded that this phase gave a better indication of sorption on sediment than either the octanol or octadecylsilane phases. 

Klausen, N. K., and Kornfelt, T. (1995). Analysis of the glycoforms of human recombinant factor Vila by capillary electrophoresis and high-performance liquid chromatography.. Chromatogr. A 718, 195-202. 

Walczak, B., Chretien, J.R., Dreux, M., Morin-Allory, L., and Lafosse, M. (1987), Factor Analysis and Experiment Design in High-performance Liquid Chromatography. IV. Influence of Mobile Phase Modifications of the Selectivity of Chalcones on an ODS Stationary Phase, Chemom. Intel. Lab. Sys., 1, 177-189. 

DK Lloyd, A Ahmed, F Pastore. A quantitative relationship between capacity factor and selector concentration in capillary electrophoresis and high-performance liquid chromatography evidence from the enantioselective resolution of benzoin using human serum albumin as chiral selector. Electrophoresis 18 958-964, 1997. 

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