Determination of DDVP in DDVP-Dipterex Formulations by Gas Chromatography

1965 ◽  
Vol 48 (6) ◽  
pp. 1115-1117
Author(s):  
John Ellis ◽  
John Bates
Keyword(s):  
Gas Chromatography ◽  
Electron Capture ◽  
Chromatographic Method ◽  
Spectrophotometric Methods ◽  
Other Substances ◽  
Gas Chromatographic Method

Abstract In the analyses of commercial fly-bait samples for DDVP (0,0-dimethyI-2,2-dichloro vinyl phosphate), containing Dipterex (0,0-dimethyl-2,2,2-trichloro - 1 - hydroxyethyl phosphonate) as a guaranteed ingredient, interferences were observed at 9.9– 10.4/t with the current spectrophotometric methods. These samples were analyzed by an electron capture gas chromatographic method, and the results showed no interference from Dipterex or other substances. A selected group of samples was analyzed by gas chromatography and spectrophotometry, and the results were compared.

Gas Chromatographic Determination of N-Butyl-N-ethyl-α,α,α-trifluoro-2,6-dinitro-p-toluidine and α,α,α-Trifluoro-2,6-dinitro-N,N-dipropyl-p-toluidine in Formulations

1971 ◽  
Vol 54 (3) ◽  
pp. 711-712
Author(s):  
Martha Fuzesi
Keyword(s):  
Gas Chromatography ◽  
Quantitative Determination ◽  
Electron Capture ◽  
Chromatographic Method ◽  
Chromatographic Determination ◽  
Electron Capture Detector ◽  
Reference Solution ◽  
Gas Chromatographic Method

Abstract A gas chromatographic method is described for the quantitative determination of N-butyl-N-ethyl-α,α,α-trifluoro-2,6-dinitro-p-tolindine and α,α,α-trifluoro-2,6-dinitro-N,N-dipropyI-p-toluidine herbicides in formulations. The sample is extracted with benzene, and equal amounts of sample and reference solution in the same concentration range are analyzed by gas chromatography, using an electron capture detector and an SE-30/Diatoport S column. The method has been applied successfully to laboratory-prepared and commercial samples.

Determination of fluoxetine and norfluoxetine in plasma by gas chromatography with electron-capture detection.

1982 ◽  
Vol 28 (10) ◽  
pp. 2100-2102 ◽  
Author(s):  
J F Nash ◽  
R J Bopp ◽  
R H Carmichael ◽  
K Z Farid ◽  
L Lemberger
Keyword(s):  
Gas Chromatography ◽  
Human Plasma ◽  
Electron Capture ◽  
Relative Error ◽  
Chromatographic Method ◽  
Linear Range ◽  
Electron Capture Detector ◽  
Electron Capture Detection ◽  
Gas Chromatographic Method

Abstract This gas-chromatographic method for assay of fluoxetine and norfluoxetine in human plasma involves extraction of the drugs and use of a 63Ni electron-capture detector. The linear range of detection is 25 to 800 micrograms/L for each drug. Overall precision (CV) in the concentration range of 10 to 100 micrograms/L for both drugs was approximately 10%. Accuracy (relative error) in the same concentration range was approximately +10%. None of the commonly prescribed antidepressants or tranquilizers that we tested interfere with the assay.

Evaluation of Electron Capture Gas Chromatographic Method for Determination of Methyl Mercury in Freezer-Case Seafoods

1984 ◽  
Vol 67 (4) ◽  
pp. 715-717
Author(s):  
George H Alvarez ◽  
George H Hight ◽  
Stephen G Capar
Keyword(s):  
Gas Chromatography ◽  
Electron Capture ◽  
Mercuric Chloride ◽  
Methyl Mercury ◽  
Chloride Solution ◽  
Chromatographic Method ◽  
Mercuric Chloride Solution ◽  
Fresh Frozen ◽  
Gas Chromatographic Method

Abstract A method was recently adopted by AOAC for determination of methylbound mercury in canned and fresh-frozen seafood by electron capture gas chromatography. That method was applied to the analysis of commercially prepared freezer-case seafoods. None of the commercially added ingredients produced electron capture responses that interfered in the analysis for methyl mercury. Recoveries of 95.7-114% were obtained in fortification studies of methyl mercury at 0.2 and 1.0 ppm levels. The applicability of aqueous methyl mercuric chloride solution for fortification studies was demonstrated.

scholarly journals The Use of Cryogenic Temperature Gas Chromatography for the Determination of Carbon Monoxide and Carbon Dioxide in Cigarette Smoke

1972 ◽  
Vol 6 (4) ◽  
Author(s):  
G.P. Morie ◽  
C.H. Sloan
Keyword(s):  
Carbon Dioxide ◽  
Gas Chromatography ◽  
Carbon Monoxide ◽  
Liquid Nitrogen ◽  
Cigarette Smoke ◽  
Cryogenic Temperature ◽  
Chromatographic Method ◽  
Porapak Q ◽  
Gas Chromatographic Method

AbstractA gas chromatographic method for the determination of carbon monoxide and carbon dioxide in cigarette smoke was developed. A column containing Porapak Q packing and a cryogenic temperature programmer which employed liquid nitrogen to cool the column to subambient temperatures was used. The separation of N

Comparison of Emmerie-Engel Method and Gas Chromatographic Method for Determination of Supplemental α-Tocopheryl Acetate in Feed Concentrates

1987 ◽  
Vol 70 (3) ◽  
pp. 417-419
Author(s):  
Michael P Labadie ◽  
Charles E Boufford
Keyword(s):  
Gas Chromatography ◽  
Vitamin E ◽  
Coefficient Of Variation ◽  
Chromatographic Method ◽  
Tocopheryl Acetate ◽  
High Potency ◽  
Gc Analysis ◽  
Gas Chromatographic Method ◽  
Official Procedure

Abstract The determination of supplemental a-tocopheryl acetate in high potency vitamin E powders and oils was compared using the Emmerie- Engel method and gas chromatography (GC). The Emmerie-Engel reaction requires saponification, extraction of the saponiflable fracaon, and quantitation by colorimetry. GC analysis requires only an extraction and/or dilution before quantitation. These are represented essentially by AOAC methods 43.147-43.151 (colorimetry) and 43.152-43.159 (GC) for high potency vitamin E concentrates. Each method was statistically evaluated for precision and sample-to-sample reproducibility. Each Emmerie-Engel value was divided by the GC value obtained for the same sample; an average of 1.049 with a coefficient of variation of 2.89% was obtained. It was concluded that (he GC procedure was superior to the Emmerie-Engel method, and ahould be the official procedure for determination of supplemental a-tocopheryl acetate in feed concentrates.

scholarly journals Gas Chromatographic Determination of Chlorothalonil in Leaves and Roots of Scrophularia and in Soil

1996 ◽  
Vol 79 (2) ◽  
pp. 587-588 ◽  
Author(s):  
Lan Zhao ◽  
De-Fang Fan
Keyword(s):  
Electron Capture ◽  
Chromatographic Method ◽  
Detection Limits ◽  
Chromatographic Determination ◽  
Soil Samples ◽  
Florisil Column ◽  
Glass Column ◽  
Leaves And Roots ◽  
Gas Chromatographic Method

Abstract A gas chromatographic method is described for determination of chlorothalonil residues in leaves and roots of Scrophularia and in soil. Samples were extracted with acetone and cleaned up on a Florisil column. Chlorothalonil residues are chromatographed directly on a glass column of 1.5% OV-17 and 2% QF-1 coated on 80-100 mesh Chromosorb W (HP) support and measured with a 63Ni electron capture detector. Detection limits are 0.001 ppm for leaf, 0.005 ppm for root, and 0.001 ppm for soil.

Capillary Column Gas Chromatographic Determination of Trace Residues of the Herbicide Chlorsulfuron in Agricultural Runoff Water

1987 ◽  
Vol 70 (4) ◽  
pp. 745-748
Author(s):  
Uaz Ahmad
Keyword(s):  
Gas Chromatography ◽  
Chromatographic Method ◽  
Capillary Column ◽  
Methylene Chloride ◽  
Chromatographic Determination ◽  
Agricultural Runoff ◽  
Runoff Water ◽  
Florisil Column ◽  
Gas Chromatographic Method

Abstract A capillary column gas chromatographic method is described for determining parts-per-trillion (ppt) levels of chlorsulfuron in agricultural runoff water. The water sample is acidified with acetic acid and extracted with methylene chloride. The chlorsulfuron in the extract is derivatized to its monomethyl derivative. After Florisil column cleanup, the methylated chlorsulfuron is determined by electron-capture gas chromatography. Recovery of chlorsulfuron from fortified water samples is greater than 80%. Detection limit of the method is 25 ng chlorsulfuron/L water (25 ppt). There are 2 reaction sites on the chlorsulfuron molecule, both of which are susceptible to methylation leading to monomethyl chlorsulfuron and dimethyl chlorsulfuron. A procedure is described to methylate selectively the sulfonamide nitrogen of chlorsulfuron.

Qualitative and Quantitative Determination of Methaqualone in Serum by Gas Chromatography

1974 ◽  
Vol 20 (2) ◽  
pp. 249-254 ◽  
Author(s):  
M A Evenson ◽  
G L Lensmeyer
Keyword(s):  
Gas Chromatography ◽  
Quantitative Determination ◽  
Chromatographic Method ◽  
Internal Standard ◽  
Serum Concentrations ◽  
Single Extraction ◽  
Qualitative And Quantitative ◽  
Gas Chromatographic Method ◽  
Isothermal Gas

Abstract A rapid, simple, accurate, and precise isothermal gas-chromatographic method is introduced for determination of methaqualone (2-methyl-3-o-tolyl-4(3H)-quinazolinone) in serum. A single extraction of 2 ml of serum, without derivative formation, will give adequate sensitivity for quantitation of therapeutic serum concentrations of the drug within 15 min. The method is free of interferences from biological substances, as well as from commonly used drugs. A non-drug internal standard compensates for variables in extraction, injection, and instrumental changes during analysis. The coefficient of variation, day-to-day, is 5.6%. Mean recovery of added methaqualone was 80%. To compensate for the nonquantitative yield and ensure accurate results, we prepared all analytical methaqualone standards in serum.

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