Rw. Reiser et al., IDENTIFICATION OF A NOVEL ANIMAL METABOLITE OF METHOMYL INSECTICIDE, Journal of agricultural and food chemistry, 45(6), 1997, pp. 2309-2313
In studies conducted to determine the fate of methomyl in goat, chicke
n, and monkey, an unknown highly polar, acidic metabolite was found in
the urine/excreta of all three animals. The metabolite was purified b
y HPLC and analyzed by microcolumn LC/MS with electrospray ionization
and by NMR. A Hypercarb porous graphitic carbon HPLC column was used f
or purification and LC/MS, since the unknown was unretained on convent
ional reversed phase HPLC columns. [C-14]Methomyl was used as radiotra
cer, and [C-13]methomyl was added at the 50% level to facilitate metab
olite identification. The molecular weight of the metabolite was deter
mined by LC/MS-electrospray, using positive and negative ionization, a
nd structurally useful fragment ions were obtained in both modes by in
-source collision-induced dissociation(CID). High-resolution accurate
mass measurements of the MH+ doublet allowed assignment of the element
al composition. NMR data showed the presence of methyl, methylene, and
methine protons with coupling observed between C-13 and the methyl an
d methine protons. From these data, the structure was determined to be
an unusual double conjugate of acetonitrile (a degradate of methomyl)
, involving conjugation with both cysteine and sulfate.