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RESEARCH PRODUCT
Zum metabolismus von dialkyldithiocarbamaten
I. NitscheKarlheinz BallschmiterF. Selenkasubject
Detection limitchemistry.chemical_classificationPrimary (chemistry)Organic Chemistrychemistry.chemical_elementGeneral MedicineMetabolismBiochemistryNitrogenIsocyanateAnalytical Chemistrychemistry.chemical_compoundSiliconechemistryUreaOrganic chemistryDithiocarbamatedescription
Abstract Metabolism dialkyldithiocarbamates. I. Determination of amines using a reaction with isocyanates followed by gas chromatographic identification of the urea derivatives formed. N,N′-Di- and N,N′,N′-trisubstituted areas, formed by the reaction of amines with isocyanates, e.g. tert. -butyl isocyanate or 3-trifluoromethylphenyl isocyanate, are useful derivatives for the gas chromatographic analysis of primary and secondary amines. The separation is carried out at temperatures between 70 and 130° on liquid phases such as silicone OV-101 and silicone OV-17. With nitrogen and electron capture detectors the detection limit is 10 10 g. Trace analysis of simple primary and secondary amines is important for the study of the metabolism of dialkyl dithiocarbamate fungicides or urea herbicides. Since secondary amines are considered to be potential precursors of cancerogenic nitrosamines their analysis is also of great importance.
year | journal | country | edition | language |
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1974-07-01 | Journal of Chromatography A |