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ARCHIVED REPORTS XR0000638
Environmental Health - Public
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EHD Program Facility Records by Street Name
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C
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CENTER
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121
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3500 - Local Oversight Program
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PR0544166
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ARCHIVED REPORTS XR0000638
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Last modified
2/22/2019 5:41:16 PM
Creation date
2/22/2019 2:12:37 PM
Metadata
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Template:
EHD - Public
ProgramCode
3500 - Local Oversight Program
File Section
ARCHIVED REPORTS
FileName_PostFix
XR0000638
RECORD_ID
PR0544166
PE
3528
FACILITY_ID
FA0005252
FACILITY_NAME
GREYHOUND LINES INC
STREET_NUMBER
121
Direction
S
STREET_NAME
CENTER
STREET_TYPE
ST
City
STOCKTON
Zip
95202
APN
13730011
CURRENT_STATUS
02
SITE_LOCATION
121 S CENTER ST
P_LOCATION
01
P_DISTRICT
001
QC Status
Approved
Scanner
WNg
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EHD - Public
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10 months in mild to moderate cases. 'out may take up to 3 years in <br /> serious cases. The threshold level at which neuropathy occurs has not <br /> been firmly established but symptoms have been observed in people <br /> exposed to concentrations ranging from 10 to 200 ppm for 9-12 months. <br /> �J <br /> In animals, signs of narcosis are seen after mice are exposed to <br /> vapor levels of 16,000 ppm for 5 minutes. Death generally occurred at <br /> concentrations between 43,800 and 52,000 ppm after 9-119 minutes. The <br /> oral LD., is cited as 24 mL/kg for 14-day-old rats and 49 mL/kg for <br /> young adult rats. <br /> Tong-term inhalation experiments in rats suggest that the first <br /> signs of neurotoxicity appear after they are exposed to levels of 200 <br /> ppm for 24 weeks. This higher threshold to induce neurotoxicity in -- <br /> animals may be due to differences in metabolism. Specifically, <br /> 2-hexanol is the chief metabolite in animals. while 2,5-hexanedione <br /> which is neurotoxic. predominates in man. Chronic topical application <br /> of a solvent containing 35.21 n-hexane caused axonal swelling and <br /> Myelin degeneration in chicks. No clinical signs were seen. Dosage <br /> was 1 g/kg/day for 64 days. In rabbits, topical application of 0.5 <br /> ML/day for up cc 10 days caused redness, irritation and scab formation. -- <br /> N-hexane is neither carcinogenic or teratogenic. One in vivo study in <br /> rats that inhaled 150 ppm for 5 days found an increased number of <br /> chromosome aberrations in the bone marrow cells. No studies an <br /> mutagenicity. reproductive toxicity or carcinogenicity in man were <br /> found (12,2930.1935) . <br /> j&gp_e_nrane <br /> Isopentane is a CNS depressant. Effects may include exhilaration, <br /> dizziness, headache, loss of appetite, nausea, confusion. inability cc <br /> do fine work. a persistent taste of gasoline and in extreme cases, loss <br /> of consciousness. Inhalation of up to 500 ppm appears to have no <br /> effect on humans. -Very high" vapor concentrations are irritating to <br /> the skin and eyes. Repeated or prolonged skin contact will dry and <br /> defac skim resulting in irritation and dermatitis. The LCs. in the <br /> mouse is estimated to be 1000 mg/L (12) . <br /> 2-Hethylvenrane (isohexane, 3-mechyipentane) <br /> No physiological data are available but isohexanes are expected to <br /> be mucous membrane irritants and to have a low oral toxicity. <br /> Ischexanes are predicted to have- narcotic properties and are documented <br /> to be cardiac sensitizers buc are not expected to have neurotoxic <br /> properties (12) . -- <br /> Cyclohexane <br /> Cyclohexane is a CNS depressant of low toxicity. Symptoms of r <br /> acute exposure are excitement, loss of equilibrium, stupor and coma. <br /> Rarely, death results due to respiratory failure. The anesthesia which <br /> is induced is weak and of brief duration bur- more potent than that <br /> 6/87 �. <br />
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