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The National Toxicology Program (NTP) recently released a report on
chronic studies of the dangers of 2-Butoxyethanol, also know as butyl
cellosolve.1 Butoxyethanol belongs to a family of glycol ethers. It
is used extensively as a solvent in surface coatings such as lacquers,
enamels, varnishes, and latex paint; in paint thinners, paint stripping
formulations, and inks; and in degreasers and industrial and household
cleaners. It was nominated for study by the UAW because of its use in
the auto industry and because of the potent toxicity of the related
chemicals ethoxy- and methoxy-ethanol. CPSC also nominated butoxyethanol
for testing.
Rats were exposed to 2-Butoxyethanol by inhalation at concentrations of 0, 31.2, 62.5, or 125 ppm for 104 weeks. A consistent exposure-related effect on the blood forming system was an exposure concentration-related anemia present at 3, 6, and 12 months, with females more affected than males. Significant increases in bone marrow cells were observed at 125 ppm. Exposure-related degeneration of the olfactory epithelium and pigmentation of the liver were observed in male and female rats at exposures as low as 31.2 ppm, the lowest dose tested. Mice were exposed to 2-Butoxyethanol by inhalation at concentrations of 0, 62.5, 125, or 250 ppm for 104 weeks. A consistent exposure-related effect on the blood forming system was an exposure concentration-related minimal anemia present at 3, 6, and 12 months, with females affected slightly more than males. Exposure related abnormal cell growth in the stomach, and pigmentation of cells in the liver, was observed at 62.5 ppm, the lowest dose tested. Damage to the nose, abnormal cell growth in the bone marrow and spleen were also observed. In genetic toxicology tests, 2-Butoxyethanol did not induce effects in the tests given. Regarding cancer, the investigators concluded that there was some evidence of carcinogenic activity in male mice based on increased incidences of hemangiosarcoma of the liver. A marginal increase in the incidences of forestomach squamous cell papilloma and an increase in the incidences of hepatocellular carcinoma may have been exposure related. There was some evidence of carcinogenic activity in female mice based on increased incidences of forestomach squamous cell papilloma or carcinoma (mainly papilloma). There was equivocal evidence of carcinogenic activity in female rats based on the increased combined incidences of benign or malignant pheochromocytoma (mainly benign) of the adrenal medulla. There was no evidence of carcinogenic activity in male rats.
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