Investigation of the reaction products of unsymmetrical dimethylhydrazine with potassium permanganate by gas chromatography-mass spectrometry

2011 ◽  
Vol 45 (4) ◽  
pp. 550-555 ◽  
Author(s):  
A. K. Buryak ◽  
T. M. Serdyuk ◽  
A. V. Ul’yanov
1990 ◽  
Vol 53 (8) ◽  
pp. 689-692
Author(s):  
YUMIKO NAKAMURA ◽  
YUKARI HASEGAWA ◽  
YASUHIDE TONOGAI ◽  
YOSHIO ITO

The concentration of residual daminozide (trade name of formulation: Alar or B-Nine) in cherries, grapes, peaches, and apples purchased in Japan was investigated using the colorimetric method. Daminozide hydrolyzes in boiling strong alkaline solution to release unsymmetrical dimethylhydrazine which is distilled and reacted with trisodium pentacyanoamine ferroate to form a specific red color at pH 4.5. This color is measured spectrophotometrically. The levels of daminozide detected were 0.07–1.39 ppm in cherries (11 samples), 0–0.36 ppm in grapes (10 samples), 0–0.42 ppm in peaches (9 samples), and 0–0.88 ppm in apples (10 samples). Furthermore, daminozide in each sample was identified as methyl daminozide by the gas chromatography/mass spectrometry (GC/MS) method.


2019 ◽  
Vol 26 (3) ◽  
pp. 213-224
Author(s):  
A Veeresham ◽  
M Sandeep ◽  
T Jagadeshwar Reddy ◽  
A Suresh Pal ◽  
K Srinivas ◽  
...  

Screening of chemicals related to chemical weapons convention including their all possible degradation and reaction products in environmental samples is important in the organization for prohibition of chemical weapons verification process. Sulfur mustards, commonly known as blistering agents, are included in schedule 1 chemicals of chemical weapons convention. Because of the presence of chlorine atoms in sulfur mustards, they are highly reactive and prone to react with other organic molecules such as phenols to produce corresponding reaction products. Thus, it is important to screen for not only the sulfur mustards but also their reaction products for verification process. The sulfur mustards and their degradation products have been routinely analyzed by gas chromatography/mass spectrometry method, however, the methods are yet to establish for the reaction products. In this study, the reaction products of the sulfur mustards with phenol (compounds 1–7) were studied by gas chromatography/mass spectrometry under electron ionization and chemical ionization conditions. The EI spectra of 1–7 displayed molecular ion and characteristic fragments that provided structure information. Mostly the fragment ions were due to homolytic cleavages involving C–O, C–S, and C–C cleavages. The methane or isobutane CI spectra showed M+., [M + H]+, and [M − H]+ ions including reagent specific adduct ions. The CI spectra also showed other adduct ions formed by association of analyte molecule with its most abundant fragment ion. The gas chromatography/retention index values were also calculated, which support unambiguous identification of targeted molecules in suspected environmental samples. The method was demonstrated for detection of the targeted molecules spiked in soil samples.


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