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8.C.e <br />Regulatory <br />History <br />Human Health <br />Assessment <br />Diquat dibromide is the common name for 6,7-dihydrodipyrido (1,2- <br />a:2',1'-c) pyrazinediium dibromide. The manufacture of diquat dibromide <br />may result in the formation of ethylene dibromide (EDB) as a process <br />impurity. EDB is considered a carcinogen, and all pesticide uses have been <br />cancelled. EPA assessed the potential exposure risks of diquat dibromide and <br />concluded in June 1986 that the presence of EDB does not pose a significant <br />dietary risk, based on worst case assumptions. In addition, the registrant <br />certified an upper limit of 10 parts per billion for EDB in diquat dibromide, <br />and demonstrated that EDB does not persist and will slowly dissipate over <br />time in diquat dibromide. <br />EPA issued a Registration Standard for diquat dibromide in June 1986 <br />(NTIS #PB87-105490). A 1991 Data Call -In required additional toxicology, <br />ecological effects, environmental fate, and residue chemistry data. Currently, <br />43 products containing the active ingredient diquat dibromide are registered <br />and marketed under the trade name Diquat. <br />Toxicity <br />In studies using laboratory animals, diquat dibromide has been shown <br />generally to be of moderate toxicity. It can cause slight to severe eye <br />irritation and has been placed in Toxicity Category II (the second highest of <br />four categories) for acute dermal and eye irritation effects. It is slightly <br />acutely toxic by the oral and inhalation routes and has been placed in Toxicity <br />Category III for these effects. Diquat dibromide causes slight dermal <br />irritation and has been placed in Toxicity Category IV for this effect. It is not <br />a skin sensitizer. <br />A supplemental subchronic dermal toxicity study using rabbits indicated <br />that diquat dibromide is toxic via repeated dermal exposure. A second dermal <br />study using rats resulted in high mortality, decreased food consumption and <br />weight gain, congestion in the lungs, liver and kidneys, and dermal irritation <br />at the application site. An inhalation study using rats resulted in increases in <br />lung weight, lung/body weight and lung/brain weight, lung lesions, and <br />mottling and reddening of the lungs in females; however, all effects except <br />the latter were reversible. A second inhalation study using rats showed no <br />effects on any of the parameters examined. <br />A chronic feeding/carcinogenicity study using rats resulted in eye <br />effects including lens opacity and severe cataracts. A feeding study using <br />beagle dogs showed some incidence of cataracts, and decreased adrenal and <br />epididymide weights in males. <br />Another chronic feeding/cancer study using rats resulted in evidence of <br />bone tumors. The Agency's Health Effects Division Reference Dose/Peer <br />Review Committee evaluated the carcinogenic potential of diquat dibromide <br />in March 1994 and classified it as a Group E carcinogen --a chemical for <br />which there is evidence of non -carcinogenicity for humans --based on a lack of <br />Attachment: EPA Facts (2109 : Dukes Root Control) <br />2 <br />Packet Pg. 56 <br />