The genotoxicity of piperonyl butoxide has been investigated in bacter
ial mutation assays using tester strains TA98, TA100, TA1535, TA1537 a
nd TA1538. The assays were conducted both with and without metabolic a
ctivation. Piperonyl butoxide was tested for mutation with and without
metabolic activation in the CHO/HGPRT assay. Chromosomal aberrations
were investigated also using Chinese hamster ovary (CHO) cells and eff
ects on DNA were evaluated by in vitro unscheduled DNA synthesis (UDS)
test using rat liver primary cell cultures. Piperonyl butoxide was no
t shown to be genotoxic in any assay system. The data presented suppor
ts the view that the liver tumors observed in rodents at dose levels a
bove the maximally tolerated dose (MTD) result from a secondary non-ge
notoxic mechanism.