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STODDARD SOLVENT 67-13<br />

to evaporate before penetrating the soil. Obviously, such an exposure<br />

scenario requires a substantial release of Stoddard solvent into the<br />

soil, <strong>and</strong> is more likely to occur if the solvent is being h<strong>and</strong>led in<br />

bulk rather than in drums.<br />

67.2.4 Other Sources of Human Exposure<br />

Data on the ambient concentrations of Stoddard solvent in air <strong>and</strong><br />

water as well as in food <strong>and</strong> drinking water are not readily available<br />

in the literature. Exposure information on some specific components<br />

may be found' in other chapters of this guide. Croups expected to<br />

receive the largest exposure to Stoddard solvent include those who use<br />

it as a solvent cleaner. Inhalation exposures are likely, as are<br />

dermal exposures if protective gloves <strong>and</strong> clothing are not worn. The<br />

same is also true for those using paints or paint thirmers that contain<br />

Stoddard solvent. Dry cleaners using Stoddard solvent can also expect<br />

to experience inhalation <strong>and</strong> dermal exposures. Although traces of the<br />

solvent may remain on clothes after dry cleaning,. inhalation <strong>and</strong> dermal<br />

exposures that result from wearing dry-cleaned clothes are not expected<br />

to be significant.<br />

67.3 HUMAN HEALTH CONSIDERATIONS<br />

67.3.1 Animal Studies<br />

67.3.1.1 Carcinogenicity<br />

There are no carcinogenicity data available for Stoddard solvent.<br />

67.3.1.2 Mutagenicity<br />

Stoddard solvent is not mutagenic in either f~ B or b m<br />

sys tame. The American Petroleum Institute evaluated Stoddard solvent<br />

in 3 tests (1914). In the Ames assay, there was no significant<br />

increase in the numbers of revertant colonies of m m<br />

strains TA98, 100, 1535, 1537 or 1538 both with <strong>and</strong> without microsomal<br />

activation. Negative results were also reported in the L5178Y mouse<br />

lymphoma assay <strong>and</strong> in a dominant lethal assay in which CD rats .were<br />

administered ip doses of 0.087, 0.289 or 0.868 ~&/kg/day for 5 days.<br />

Cochet pf &. (1968) reported negative results in the micronucleus test<br />

on mouse bone marrow cells <strong>and</strong> in the 19 m induction of sister<br />

chromatfd exchange in human lympohocytes.<br />

67.3.1.3 Teratogenicity, Embryotoxicity <strong>and</strong> Reproductive Effects<br />

In one study, there wore no treatment-related effects on<br />

Lm<strong>plan</strong>tation, fetal resorption or number of viable femme after mated<br />

female CD rate were exposed to vapor levels of 100 or 300 ppm 6 hours<br />

daily on days 6 through 15 of gestation. In the high exposure group<br />

there was a statistically significant increase in the total incidence<br />

of fetuses with ossification variation but the types <strong>and</strong> relative<br />

6/87

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