Desethyl atrazine and desethyl terbutylazine, the degradation products
of two commonly encountered pesticides, were investigated by UV spect
rophotometric and electrochemical techniques. In a sufficiently acidic
environment, both compounds undergo further redox degradation which i
nvolves the cleavage of the chlorine atom. The reaction is pH dependen
t and proceeds via the protonated forms of both compounds. Spectrophot
ometric data indicate that the pH required for this reaction is about
one unit lower than that required for the degradation of the parent pe
sticides, (C) 1998 Academic Press.