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Human Health Risk Assessment <br /> 0 <br /> Former Mobil Oil Bulk Plant 04-343 I <br /> 500 East Grant Line Road <br /> Tray, California <br /> r effects (API, 1986). The IARC (1982) reports that a relationship between benzene and acute <br /> myelogenous leukemia has been established in epidemiological stt dies performed among <br /> shoemakers and workers in the rubber, printing, and petroleum industries. These studies have <br /> been criticized, however, particularly regarding the association of the in ,deuce of leukemia with <br /> ' the low concentrations of benzene measured in these industries (API, 1986). Benzene has been <br /> placed into Group A, "known human carcinogen," under the EPA weight-of-evidence <br /> classification. <br /> I <br /> 3.3 TOLUENE <br /> Toluene is a monocyclic aromatic hydrocarbon (C6H5CH3) with a mol,•..;ular weight of 92.1. It <br /> is the lowest molecular weight member of the alkylbenzenes. Alkylbet�,%:nes, in general, possess <br /> properties similar to those described for benzene. Toluene is found in gasoline at concentrations <br /> ' ranging from approximately 3 to 22 percent (CLUFTFM, 1989). Alkti. - substitutions change the <br /> physical characteristic of toluene and, in turn, alter its absorption, partition, and metabolic <br /> properties. Toluene is a clear, colorless liquid with a pungent, benzene-like odor (EPA, 1985b). <br /> It is only slightly soluble in water, and is soluble in alcohol, ether, chloroform, acetone, glacial <br /> acetic acid, and carbon disulfide (Merck, 1989). Chemical processes and photochemical <br /> ' processes appear unlikely to compete significantly with volatilizatio;) and biodegradation as <br /> removal processes (EPA, 1985b). The physical and chemical pn iperties of toluene are <br /> summarized in Table 3--5. <br /> Toluene is readily absorbed in the lungs as a vapor and in the gastroin,estinal tract as a liquid. <br /> Once absorbed, the major excretory pathway is rapid oxidation of toluene to benzoic acid, which <br /> is conjugated with glycine and excreted as hippuric acid in urine. E:._cretion of hippuric acid <br /> ' may be proportional to exposure (Doull et al., 1980). Toluene ma ., be eliminated through <br /> respiration. Inspired toluene has an estimated biological half-life of 0.083 days <br /> ' (Cleland and Kingsbury, 1977). <br /> The odor threshold of toluene is 10.15 ppm, and at concentrations bef.,veen 300 and 400 ppm, <br />' eye irritation is experienced (OSHA, 1978). Perceptual speed is not significantly affected until <br /> exposure exceeds 700 ppm for a period of 20 minutes (EPA, 1985b). Evidence indicates that <br /> 30-0136-11 <br /> i 3-10 <br /> i <br />