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SU0006659 SSCRPT
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SU0006659 SSCRPT
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Entry Properties
Last modified
5/7/2020 11:32:38 AM
Creation date
9/9/2019 10:40:26 AM
Metadata
Fields
Template:
EHD - Public
ProgramCode
2600 - Land Use Program
FileName_PostFix
SSCRPT
RECORD_ID
SU0006659
PE
2622
FACILITY_NAME
PA-0700352
STREET_NUMBER
11450
Direction
E
STREET_NAME
TOKAY COLONY
STREET_TYPE
RD
City
LODI
Zip
95240
APN
06319020
ENTERED_DATE
7/31/2007 12:00:00 AM
SITE_LOCATION
11450 E TOKAY COLONY RD
RECEIVED_DATE
7/31/2007 12:00:00 AM
P_LOCATION
99
P_DISTRICT
004
QC Status
Approved
Scanner
SJGOV\rtan
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\MIGRATIONS\T\TOKAY COLONY\11450\PA-0700352\SU0006659\SSC RPT.PDF
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EHD - Public
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;XTOXNET PIP - ESFENVALERATP Page 2 o: <br /> L S./ <br /> ,ercentage of the one insecticidally active isomer(84% for esfenvalerate and 22% for fenvalerate). <br /> toxicological Effects: <br /> . Acute toxicity: Esfenvalerate is a moderately toxic compound via the oral route. The reported oral LD50 of <br /> esfenvalerate is 458 mg/kg in rats. It is slightly toxic via the dermal route, with a reported dermal LD50 of 2500 <br /> mg/kg in rabbits. It is practically non-toxic via inhalation,with a reported inhalation LC50 of greater than 2.93 <br /> mg/L in rats [2,12]. Because esfenvalerate is a relatively new compound it has little usage history. The bulk of <br /> evidence related to acute poisonings in humans due to esfenvalerate comes from incidents in India. Nearly 600 <br /> individual cases of poisoning were reported between 1982 and 1988. These cases were due to improper handling c <br /> the pesticide. Acute toxic effects were observed in workers and among the general public. Symptoms of acute <br /> poisoning included dizziness, burning and itching (which was worsened by sweating and washing). Severe cases c <br /> direct contact caused blurred vision, tightness in the chest, and convulsions (2). The changes appear to be <br /> reversible. In rats, high acute exposure to esfenvalerate produced muscle incoordination, tremors, convulsions, <br /> nerve damage, and weight loss. The compound may produce nausea, vomiting, headache, temporary nervous <br /> system effects such as weakness, tremors, and incoordination at acute exposure levels in humans. Esfenvalerate is <br /> strong eye irritant,producing tearing or blurring of vision. <br /> . Chronic toxicity: Rats fed fenvalerate at concentrations of approximately 12.5 mg/kg/day for two years had no <br /> compound-related changes in the blood or urine [12]. In other studies significant reduction in body weight was the <br /> main adverse effect seen in both rats and mice of both sexes. <br /> . Reproductive effects: In a three-generation rat study, low doses (up to 12.5 mg/kg/day) of fenvalerate produced r <br /> toxicity in the fetus. Some maternal toxicity was noted in the second generation at the higher dose. When pregnani <br /> mice and rabbits were fed low dietary levels of fenvalerate (2.5 mg/kg/day) on days 6 to 15 of gestation, there was <br /> maternal toxicity in both species. It seems that during pregnancy, the females are more sensitive to fenvalerate tha <br /> they would otherwise be, even though the toxicity is not reflected in any effect on the fetus [5]. There are no <br /> specific data available for esfenvalerate, but it is not expected to cause reproductive effects at low doses. <br /> . Teratogenic effects: Esfenvalerate did not produce any birth defects in offspring at low dietary doses [2]. It appe� <br /> the the pesticide would not pose a teratogenic threat to humans at expected exposure levels. <br /> . Mutagenic effects: Esfenvalerate shows no mutagenic effects. Numerous tests in hamsters, mice and rats show nc <br /> signs of mutagenic activity associated with this compound [2]. It is likely that it poses no mutagenic risk to humar. <br /> . Carcinogenic effects: A rat study of fenvalerate conducted over a wide range of doses of up to 75 mg/kg, for two <br /> years, resulted in no evidence of cancer. Mice fed diets containing small amounts of fenvalerate for two years <br /> showed no adverse effects [2]. It appears that fenvalerate does not cause cancer. <br /> . Organ toxicity: Studies to date have not shown any dose-related effects on internal organs of test animals or in <br /> human populations [2]. <br /> . Fate in humans and animals: Cows treated with 0.1 or 0.5 g fenvalerate on their skin had 0.03 to 0.06% of the <br /> applied chemical in the milk. When the cows received fenvalerate orally at very low levels, about 0.50%of the do <br /> appeared in the milk. Fenvalerate does not appear to be metabolized by bovine rumen,but it is degraded further <br /> down the digestive tract [32]. This happens rapidly with less than 0.02% of the parent compound found in the urin <br /> and 20% of the major metabolite present. Higher concentrations of the parent compound are present in the feces. I <br /> the rat, fenvalerate is rapidly broken down and almost completely eliminated within several days. One study <br /> indicated mammals eliminated 96% in the feces in 6 to 14 days [32]. While the data presented here are for <br /> fenvalerate, esfenvalerate behaves in the same manner [33]. <br /> Ecological Effects: <br /> . Effects on birds: Esfenvalerate is slightly toxic to birds. Oral LD50 values for the compound are 1312 mg/kg in <br /> bobwhite quail and greater than 2250 mg/kg in mallard ducks [12]. <br /> . Effects on aquatic organisms: Based on laboratory studies, fish are very sensitive to esfenvalerate. It has a 96- <br /> ,ttp:Hextoxnet.orst.edu/pips/esfenval.htm 6/25/20, <br />
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