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ARCHIVED REPORTS_XR0003232
Environmental Health - Public
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EHD Program Facility Records by Street Name
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2900 - Site Mitigation Program
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PR0505148
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ARCHIVED REPORTS_XR0003232
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Entry Properties
Last modified
2/5/2020 6:30:43 PM
Creation date
2/5/2020 2:56:41 PM
Metadata
Fields
Template:
EHD - Public
ProgramCode
2900 - Site Mitigation Program
File Section
ARCHIVED REPORTS
FileName_PostFix
XR0003232
RECORD_ID
PR0505148
PE
2950
FACILITY_ID
FA0003950
FACILITY_NAME
SJ COUNTY GARAGE
STREET_NUMBER
130
Direction
N
STREET_NAME
HUNTER
STREET_TYPE
ST
City
STOCKTON
Zip
95202
CURRENT_STATUS
02
SITE_LOCATION
130 N HUNTER ST
P_LOCATION
01
QC Status
Approved
Scanner
SJGOV\sballwahn
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EHD - Public
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U <br /> i <br /> it may be appropriate to prevent exposure during pregnancy GENETIC TOXICITY 1 CARCINOGENICITY Xylene was <br /> not genotoxic in several mutagenicity testing assays including the Ames test In a cancer study sponsored by the National <br /> Toxicology Program (NTP),technical grade xylene gave no evidence of carcinogenicity in rats or mice dosed daily for two <br /> years HEARING Mixed xylenes have been shown to cause measurable hearing loss in rats exposed to 800 ppm in the <br /> air for 14 hours per day for six weeks Exposure to 1450 ppm xylene for 8 hours caused hearing loss while exposure to <br /> 1700 ppm for 4 hours did not Although no information is available for lower concentrations, other chemicals that cause <br /> hearing loss in rats at relatively high concentrations do not cause hearing loss in rats at low concentrations Worker <br /> exposure to xylenes at the permissible exposure limit(100 ppm,time-weighted average) is not expected to cause hearing <br /> loss <br /> This product contains ETHYLBENZENE <br /> BIRTH DEFECTS AND REPRODUCTION Ethylbenzene is not expected to cause birth defects or other developmental <br /> effects based on well-conducted studies in rabbits and rats sponsored by NIOSH Other studies in rats and mice,which <br /> reported urinary tract malformations, have many deficiencies and have limited usefulness in evaluating human risk <br /> Reproductive effects are not expected based on a N IOSH study of fertility, and lack of effects observed for sperm counts <br /> and motility,estrous cycle and pathology of reproductive organs following repeated exposures HEARING Ethylbenzene <br /> caused probable hearing loss in rats exposed to 400 ppm for 8 hr/day for 5 days based on increases in auditory <br /> thresholds and loss of inner ear hair cells At 300 ppm, there was loss of inner ear hair cells without any effect on auditory <br /> thresholds There is no evidence of hearing loss in people GENETIC TOXICITY Ethylbenzene tested negative in the <br /> bacterial mutation test, Chinese Hamster Ovary(CHO) cell in vitro assay, sister chromatid exchange assay and an <br /> unscheduled DNA synthesis assay Conflicting results have been reported for the mouse lymphoma cell assay <br /> Increased micronuclei were reported in an in vitro Syrian hamster embryo cell assay, however,two in vivo micronuclei <br /> studies in mice were negative In Syrian hamster embryo cells in vitro,cell transformation was observed at 7 days of <br /> incubation but not at 24 hours Based on these results, ethylbenzene is not expected to be mutagenic or clastogenic <br /> CARCINOGENICITY In studies conducted by the National Toxicology Program, rats and mice were exposed to <br /> ethylbenzene at 25, 250 and 750 ppm for six hours per day,five days per week for 103 weeks In rats exposed to 750 <br /> ppm,the incidence of kidney tubule hyperplasia and tumors was increased Testicular tumors develop spontaneously in <br /> nearly all rats if allowed to complete their natural life span, in this study,the development of these tumors appeared to be <br /> enhanced in male rats exposed to 750 ppm In mice,the incidences of lung tumors in males and liver tumors in females <br /> exposed to 750 ppm were increased as compared to control mice but were within the range of incidences observed <br /> historically in control mice Other liver effects were observed in male mice exposed to 250 and 750 ppm The incidences <br /> of hyperplasia were increased in the pituitary gland in female mice at 250 and 750 ppm and in the thyroid in male and <br /> female mice at 750 ppm <br /> SECTION 12 ECOLOGICAL INFORMATION <br /> ECOTOXICITY <br /> This material is expected to be toxic to aquatic organisms <br /> The 96 hour(s) LC50 for rainbow trout ( Salmo garrdnen) is 8 2 mg/I <br /> The 96 hour(s) LC50 for bluegill sunfish ( Lepomis macrochlrus) is 13 mg/I <br /> The 96 hour(s) LC50 for fathead minnow( Prmephales promelas) is 27 mg/I <br /> ENVIRONMENTAL FATE <br /> This material is expected to be readily biodegradable <br /> More than 99% of xylene released to the environment is volatilized to the atmosphere Xylene is readily biodegradable, <br /> the rate of biodegradation varies with the source of microbial culture and whether acclimation to the substrate has been <br /> accomplished by pre-exposure to xylene <br /> SECTION 13 DISPOSAL CONSIDERATIONS <br /> Use material for its intended purpose or recycle if possible This material, if it must be discarded, may meet the criteria of <br /> a hazardous waste as defined by US EPA under RCRA(40 CFR 261)or other State and local regulations Measurement <br /> • Revision Number 1 6 of 9 MIXED XYLENES <br /> Revision Date 01/08/2003 MSDS PE0014 <br />
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