Trinitrotoluene (TNT) and related compounds were tested for induction of mu
tation in the CHO-hprt mutation assay. The parent compound, TNT, was consis
tently found to be mutagenic at concentrations above 40 mug ml(-1), whether
or not S9 activating enzymes were added. Five TNT metabolites gave statist
ically significant but small increases in mutation frequency over solvent c
ontrols: 4-amino-2,6-dinitrotoluene, 2,4',6,6'-tetranitro-2',4-azoxytoluene
, 2,2',6,6'- tetranitro-4,4'-azoxytoluene, 2',4,6,6'-tetranitra-2,4'-azoxyt
oluene and triaminotoluene. Clear dose-response relationships could not be
established for the mutagenic response of these compounds. They are conside
red as very weak mutagens in this mammalian test system. Five compounds did
not produce statistically significant mutation frequencies at the levels t
ested: 2-amino-4,6-dinitrotoluene, 2,4-diamino-6-nitrotoluene, 1,3,5-trinit
robenzene, 2,6-diamino-4-nitrotoluene and 4,4',6,6'-tetranitro-2,2'-azoxyto
luene. The results indicate that none of the TNT metabolites tested pose a
significant mutational health risk, at least as judged by the CHO-hprt assa
y. Copyright (C) 2000 John Wiley & Sons, Ltd.