-
Categories
-
Pharmaceutical Intermediates
-
Active Pharmaceutical Ingredients
-
Food Additives
- Industrial Coatings
- Agrochemicals
- Dyes and Pigments
- Surfactant
- Flavors and Fragrances
- Chemical Reagents
- Catalyst and Auxiliary
- Natural Products
- Inorganic Chemistry
-
Organic Chemistry
-
Biochemical Engineering
- Analytical Chemistry
-
Cosmetic Ingredient
- Water Treatment Chemical
-
Pharmaceutical Intermediates
Promotion
ECHEMI Mall
Wholesale
Weekly Price
Exhibition
News
-
Trade Service
Microwave-assisted extraction (MAE) is a simple, fast, and accurate method developed for the analysis of
N,N
-dimethyldithiocarbamate (DMDTC) and ethylenebis(dithiobamate) (EBDTC) fungicides in fruits and vegetables. Residues are extracted from the plant matrices and hydrolyzed to CS
2
in a single step in the presence of 1.5% SnCl
2
in 5
N
hydrochloric acid using a laboratory microwave oven operated in the closed-vessel mode. The evolved CS
2
, trapped in a layer of isooctane overlaying the reaction mixture, is analyzed by gas chromatography/flame photometric detection (GC/FPD). Sets of 12 samples are processed simultaneously. Quantification is based on external standard calibration curves made with either standard solutions of individual DMDTCs (thiram, ziram) or EBDTCs (maneb, zineb, mancozeb), which are processed as the field samples, or using standard solutions of CS
2
made in isooctane. Calibration curves are better fitted with quadratic equations with correlation coefficients >0.999; however, good linear correlation coefficients can also be obtained in narrower calibration ranges. Limits of detection (LODs) and limits of quantitation (LOQs) are in the range 0.005–0.1 mg/kg. Recoveries are >80%, with respective relative standard deviation values <20%.