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:XTOXNET PIP - IPRODIONE Page 2 0: <br /> beagle dogs fed dietary doses of about 2.3 mg/kg/day for 1 year showed liver and kidney weight increases. At dos <br /> starting at about 1.5 mg/kg/day, the dogs had decreased prostrate weights and changes within red blood cells <br /> (damage to the hemoglobin molecules). Females also had slight decreases in uterus weights. No effects were note( <br /> below 0.5 mg/kg/day dose [43]. <br /> • Reproductive effects: Female rats were fed iprodione over three successive generations showed no effects on <br /> reproduction at doses at and below 1.25 mg/kg/day [43]. Reductions in fertility and fecundity were not observed a <br /> doses of 5 mg/kg/day [43]. Based on these data, ioprodione is not likely to cause reproductive effects. <br /> • Teratogenic effects: There were no developmental effects noted in the offspring of pregnant rats receiving dietar; <br /> doses of about 5.4 mg/kg/day [43]. However, the dose rate of about 120 mg/kg/day elicited unspecified <br /> developmental toxicity in the rats [43]. Rabbits did not develop any dose-related toxicity at or below 2.7 mg/kg/da <br /> of iprodione,but did develop toxicity at 6 mg/kg/day [43]. It appears that iprodione is not likely to cause teratoger <br /> effects at expected exposure levels. <br /> • Mutagenic effects: No data are currently available. <br /> • Carcinogenic effects: A 2-year feeding experiment with rats showed no increases in tumor formation or tumor <br /> precursors(neoplastic foci) at dietary doses of about 2.5 mg/kg/day [43]. An 18-month study in mice showed <br /> cancer related effects at doses up to approximately 22 mg/kg/day [43]. Current evidence on the carcinogenicity of <br /> iprodione is inconclusive. <br /> • Organ toxicity: Target organs identified in animal studies include the reproductive system (prostate gland and <br /> uterus), liver, and kidneys. <br /> • Fate in humans and animals: No data are currently available [43]. <br /> :colouical Effects: <br /> • Effects on birds: Iprodione is slightly toxic to wildfowl. The reported acute oral LD50 in bobwhite quail is 930 <br /> mg/kg [1]. <br /> • Effects on aquatic organisms: Iprodione is moderately toxic to fish species, with LC50 values ranging from 2.25 <br /> mg/L in the sunfish to 6.7 mg/L in the rainbow trout [8]. Reported bioconeentration factors of 50 to 360 in carp an <br /> other fish species indicate low bioconcentration potential [8]. <br /> • Effects on other organisms: Iprodione is nontoxic to bees [1]. <br /> Mvironmental Fate: <br /> • Breakdown in soil and groundwater: The half-life of iprodione in soil ranges from less than 7 to greater than 60 <br /> days [l,l 11. A representative half-life in most soils is estimated to be 14 days [11]. Degradation rates vary with so' <br /> acidity, soil clay content, and history of the soil fungicide treatment. In soils that had been treated consistently wit] <br /> iprodione for 10 or more years, slow or little breakdown of the compound vinclozolin occurred, while in soil that <br /> had been treated with vinclozolin rapid degradation of vinclozolin and iprodione occurred [44]. Iprodione is slight <br /> soluble and moderately to well sorbed by most soils [11]. These properties, combined with its short field half-life <br /> indicate a low potential to contaminate groundwater. <br /> • Breakdown in water: The compound breaks down very rapidly in water under aerobic conditions;the rate is <br /> lesser, but still rapid under near-anaerobic conditions [8]. The compound is readily degraded by UV light. <br /> • Breakdown in vegetation: The compound is rapidly broken down in the plant after is taken up by the roots and <br /> translocated [1]. The main metabolite in plants is 3,5-dichloroaniline [1]. Iprodione alone or in combinations with <br /> several other fungicides was not toxic to plants (phytotoxic) [45]. <br /> "hysical Properties: <br /> • Appearance; Iprodione is a colorless,odorless crystal [1]. <br /> . Chemical Name: 3-(3,5-dichlorophenyi)-N-(1-methylethyl)2,4-dioxo-l-imidazoline-carboxamide [1] <br /> tttp://extoxnet.orst.edu/pips/iprodion.htm 7/2/20( <br />