Study of the Performances of Thin Layer Chromatography. IV--Optimization of Experimental Conditions

1979 ◽  
Vol 17 (7) ◽  
pp. 368-386 ◽  
Author(s):  
G. Guiochon ◽  
F. Bressolle ◽  
A. Siouffi
1980 ◽  
Vol 58 (7) ◽  
pp. 723-726 ◽  
Author(s):  
Patricia F. Currie ◽  
J. Wilson Quail ◽  
John A. Weil

The reaction between 2,2-diphenyl-1-picrylhydrazyl and bromine in solution bas been studied at several temperatures. Despite the literature, reporting simple phenyl bromination products, a substantial yield of nitration products is observed. These have been identified by use of thin-layer chromatography, mass spectrometry, nuclear magnetic resonance, and elemental analysis. Among various products, 2-(p-nitrophenyl)-2-phenyl-1-picrylhydrazine is a major one at room temperature and above. It is thought that this compound is formed by reaction of DPPH with NO2, displaced from ortho nitro groups in the picryl rings by bromine. Yields were found to vary, depending on experimental conditions, with the temperature and the rate of bromine addition as primary controlling factors.


2005 ◽  
Vol 88 (1) ◽  
pp. 70-79 ◽  
Author(s):  
Anna Maślanka ◽  
Jan Krzek

Abstract A thin-layer chromatography (TLC)-densitometry method has been developed to identify and quantify haloperidol, amitriptyline, sulpiride, promazine, fluphenazine, doxepin, diazepam, trifluoperazine, clonazepam, and chlorpromazine in selected psychotropic drugs. Separation was performed on precoated silica gel 60 F254 TLC plates. Chromatograms were developed in various mobile phases, and 8 of 30 tested phases were selected based on spot location and developing time. The identification and quantification were carried out based on ultraviolet densitometric measurements at chosen wavelengths. In addition to retention coefficients, the absorption spectra recorded directly from chromatograms were also used in qualitative analysis. Under established experimental conditions, high sensitivity of the method was achieved. The limit of detection ranged from 0.009 to 0.260 μg, depending on the wavelength selected for measuring. A satisfactory recovery, ranging from 92.99 to 104.70%, was achieved for individual constituents.


Author(s):  
H. R. Bolliger ◽  
M. Brenner ◽  
H. Gänshirt ◽  
Helmut K. Mangold ◽  
H. Seiler ◽  
...  

1969 ◽  
Vol 61 (4) ◽  
pp. 641-648 ◽  
Author(s):  
Leon J. Sholiton ◽  
Emile E. Werk

ABSTRACT Rat and bovine brain have been incubated with testosterone-4-14C under standard conditions. With use of paper chromatography, the extracted metabolites were noted to fall into less-polar, iso-polar, and more polar fractions. The components of the less-polar fraction were separated by acetylation and thin-layer chromatography and the major end-products identified by recrystallization to constant specific activity or constant 3H/14C ratios. Androst-4-enedione and 5α-dihydrotestosterone were formed consistently under the conditions utilized. Trace amounts of other less-polar metabolites were noted occasionally.


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