Comparison of several liquid phases in gas liquid chromatography of methyl parathion and metabolites

1970 ◽  
Vol 5 (2) ◽  
pp. 98-103 ◽  
Author(s):  
P. S. Jaglan ◽  
F. A. Gunther
1976 ◽  
Vol 59 (4) ◽  
pp. 740-744
Author(s):  
Edwin R Jackson

Abstract Methyl parathion formulations (a synthetic sample, a technical material, and 6 emulsifiable concentrates) were analyzed by high-performance liquid chromatography (HPLC), gas-liquid chromatography (GLC), and infrared (IR) spectroscopy. The HPLC method used in ultraviolet detector and a Permaphase ODS column with a methanol-water mobile phase. The GLC method used an SE-30/OV-210 column and flame ionization detection. The IR spectrum was recorded at 8.16 μm. A synthetic sample formulated to contain 45.5% methyl parathion (analytical grade) was analyzed 8 times by each method. HPLC yielded an average value of 45.4%, GLC 45.9%, and IR 45.7%. Analyses of variance of this repeatability study showed that the differences between the GLC mean and both the theoretical value and the HPLC mean were small, but significant. Technical methyl parathion and 6 emulsifiable concentrates were analyzed in duplicate by each method. Variance calculations for each set of duplicates by each method indicate a high probability of difference in the methods. High results from the IR analysis are probably due to impurities in the technical material because analysis of the synthetic sample was satisfactory. The HPLC and GLC methods appear to be precise and will be studied collaboratively.


1960 ◽  
Vol 38 (5) ◽  
pp. 631-640 ◽  
Author(s):  
E. von Rudloff

A study has been made of the degree of separation of mixtures of some terpene hydrocarbons, some of their oxygenated derivatives, two sesquiterpene alcohols, and three monophenols on a variety of columns. Temperature and sample size affected the degree of separation and the solid support Chromosorb W, a calcined diatomaceous earth, was found to combine the advantages of Celite and C-22 firebrick without causing decomposition of the sample at higher temperatures. When Craig polyesters were used as liquid phases, separations equal to those obtained on polyethylene glycol were realized with the added advantage that these produced columns which are stable at 190 to 220 °C. Consequently, sesquiterpene alcohols and monophenols were also separated successfully. Another useful liquid phase for both low and high temperatures was found in a meta-linked polyphenyl ether. Squalene was found to be an efficient liquid phase for the separation of terpene hydrocarbons at 130 °C and lower. The possible application of the present findings for preparative work is discussed.


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