Methylation of a wide range of organic acids with methyl iodide was si
mply and efficiently performed on anion exchange resins with either su
percritical carbon dioxide or acetonitrile as solvents. Analytes inclu
ding chlorophenoxyacetic acids, pentachlorophenol, and quinoxaline-2-c
arboxylic acid were displaced from the resin in a single step as their
methyl esters or ethers in high yield using the supercritical fluid e
xtraction (SFE) system, The conversion of 2,4-D and 2,4,5-T (solutions
of 100 and 35 ppb, respectively) to their methyl esters was complete
in 30 min and gave yields of 92% and 99% with coefficients of variatio
n of 10%. Analytes in up to 200 mt of aqueous solution could be trappe
d on 0.1 g of AG MP-1 anion exchange resin and derivatized and eluted
using methyl iodide in supercritical carbon dioxide at 200 bar and 80
degrees C, Less acidic compounds including albendazole, fenbendazole,
triclabendazole, and sulfadimidine could also be derivatized on the re
sin under SFE conditions or in a quick and inexpensive procedure using
acetonitrile; however, these compounds gave lower yields and multiple
methylated products.