Related Experiment Video
Updated: Aug 19, 2026

Functional Characterization of Carboxylesterases in Insecticide Resistant House Flies, Musca Domestica
Published on: August 23, 2018
Methylene retention indexes for isolated toxaphene congeners
J G McDonald1, W Vetter, R A Hites
1Environmental Science Research Center, School of Public and Environmental Affairs and Department of Chemistry, Indiana University, Bloomington 47405, USA.
Abstract:
Toxaphene was a heavily used, broad-spectrum insecticide, which was banned in most countries in the 1980s. Early data suggested that a limited number of congeners in the technical mixture were responsible for its toxicity to insects. However, toxaphene research has historically focused on analyzing total toxaphene, largely due to insufficient analytical methodology to measure the individual congeners. In recent years, congener-specific toxaphene research has flourished due to analytical advances leading to the identification of several congeners, about 25 of which are commercially available. However, the high price of these standards may inhibit toxaphene research in some laboratories. We report here the methylene retention indexes for 28 isolated toxaphene congeners. When used in conjunction with mass spectrometry, methylene retention indexes provide an alternative method for identifying these compounds when direct comparison with standard compounds is not practical.
More Related Videos
10:35Study on the Metabolism of Six Systemic Insecticides in a Newly Established Cell Suspension Culture Derived from Tea (Camellia Sinensis L.) Leaves
Published on: June 15, 2019
04:17Analysis of Organochlorine Pesticides in a Soil Sample by a Modified QuEChERS Approach Using Ammonium Formate
Published on: January 20, 2023
Related Concept Videos
NMR Spectroscopy of Benzene Derivatives
Mass Spectrometry: Cycloalkane Fragmentation
For example, cyclohexane molecular ions have a mass-to-charge ratio (m/z) of 84, which tends to produce a stronger signal than linear alkanes like hexane. This stability comes from...
Mass Spectrometry: Aromatic Compound Fragmentation