scholarly journals Gas-liquid chromatography of dialkyl, alkyl acyl, and diacyl derivatives of glycerol

1969 ◽  
Vol 10 (1) ◽  
pp. 128-131
Author(s):  
Randall Wood ◽  
W.J. Baumann ◽  
Fred Snyder ◽  
H.K. Mangold
1978 ◽  
Vol 24 (4) ◽  
pp. 669-674 ◽  
Author(s):  
P Purkiss ◽  
R C Hughes ◽  
R W Watts

Abstract A method for screening urine for abnormalities in glycoconjugate excretion is presented. An oligosaccharide-containing fraction is isolated from urine by gel chromatography and the carbohydrate-containing components in this fraction are degraded to monosaccharides, suitable derivatives of which are analyzed by gas-liquid chromatography. A pattern which characterizes the monosaccharides originating in complex carbohydrates in urine is thus obtained. Data obtained by applying this method to normal subjects in various age groups are presented and the applicability of the method and its limitations are illustrated by the use of examples from patients with previously diagnosed disorders of glycoconjugate metabolism.


1981 ◽  
Vol 64 (6) ◽  
pp. 1470-1473
Author(s):  
Patrick Haché ◽  
René Marquette ◽  
Gilles Volpé ◽  
Victorin N Mallet

Abstract A simple method is described for the fast recovery of fenitrothion, an organophosphorus insecticide, from soil, chicken liver, urine, clams, and pine needles. The substrate is homogenized with acetonitrile or methanol, diluted with water, and passed through a column containing Amberlite XAD-7. Fenitrothion is recovered quantitatively by eluting with 4 portions of 25 mL ethyl acetate. After evaporation, the compound is determined quantitatively by gas-liquid chromatography with a flame photometric detector. The procedure is also suitable for some derivatives of fenitrothion, namely, fenitrooxon and S-methylfenitrothion. As low as 0.05 ppm of the parent compound may be determined.


1969 ◽  
Vol 47 (21) ◽  
pp. 4091-4093 ◽  
Author(s):  
M. B. Perry ◽  
Ann C. Webb

The mono-, di-, and tri-O-methyl ether derivatives of 2-amino-2-deoxy-D-glucopyranose have been analyzed by gas–liquid chromatography of their fully acetylated 2-acetamido-2-deoxy-D-glucitol derivatives which were prepared from the glycoses by reduction with sodium borohydride followed by acetylation with acetic anhydride. The methyl ethers of 2-amino-2-deoxy-D-glucopyranose were also characterized by degradation with ninhydrin to the corresponding methyl ether derivatives of D-arabinose which were identified by paper chromatography.


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