A comprehensive DTA study of some 40 different binary phenol systems i
nvolving the 'in situ' formation of the p-nitrobenzoylchloride, p-phen
ylazobenzoylchloride or 3,5-dinitrobenzoylchloride derivatives, has re
vealed that for most of these systems, well-resolved endotherms appear
in the DTA profiles corresponding to the melting points of the consti
tuent phenols and of the respective derivatives. Thus this procedure i
s of sufficient versatility for the identification of phenols in a bin
ary mixture. The general method involves adding the chosen acid chlori
de to the solid-state binary phenol mixture and obtaining the correspo
nding DTA profile, which is subsequently compared with those in a bank
for phenols, binary phenol mixtures and binary phenol derivative mixt
ures. The method offers rapid identification of phenols in the solid s
tate.