Journal of AOAC International 93 (6), 1957-1964, 2010.

A Fast, Inexpensive, and Safe Method for Residue Analysis of Meptyldinocap in Different Fruits by Liquid Chromatography/Tandem Mass Spectrometry

KAUSHIK BANERJEE, SOMA DASGUPTA, and MANJUSHA R. JADHAV
National Research Centre for Grapes, Manjri Farm, Pune, Maharashtra, India 412307
DATTATRAYA G. NAIK
Agharkar Research Institute, Pune-411004, India
AXEL PATRICK LIGON
Am Surck 55, 44225 Dortmund, Germany
DASHARATH P. OULKAR, RAHUL H. SAVANT, and PANDURANG G. ADSULE
National Research Centre for Grapes, Manjri Farm, Pune, Maharashtra, India 412307

Received: February 16, 2010

Acceped: March 26, 2010

Abstract:

An analytical method is reported for residue analysis of the fungicide meptyldinocap in different fruit matrixes that involves extraction with ethyl acetate, hydrolysis of the residues with ethanolamine, and determination by LC/MS/MS. The method involves extraction of 10 g sample with 10 mL ethyl acetate; evaporation of the ethyl acetate phase to dryness, and subsequent hydrolysis of the residues to 4,6-dinitro-2- (1-methylheptyl) phenol on reaction with 1% ethanolamine. The pH of this hydrolyzed product was neutralized with formic acid and analyzed by LC/MS/MS. The hydrolysis reaction followed pseudo-first-order kinetics, and the reaction product was spectroscopically confirmed as 2-(1-methylheptyl)-4,6-dinitrophenol. The method offered >80% recoveries at an LOQ of 10 ng/g for grape and mango, 25 ng/g for pomegranate with intralaboratory Horwitz ratio <0.5, and measurement uncertainties <10% at LOQ levels. Considering first-order rate kinetics, activation energy, enthalpy of activation, and entropy of activation varied as solvent > mango > grape > pomegranate. Free energy of activation at 298 K was higher than at 280 K and was similar for solvent and three matrixes at both temperatures.