Abstract |
Methyl n-butyl ketone (MBK) was considered rather harmless until an outbreak of peripheral neuropathy occurred in 1973 among workers exposed to MBK. MBK easily penetrates the skin; pulmonary retention is approximately 80-85% in man. Distribution is widespread with highest levels in blood and liver; MBK also reaches the fetal tissues. MBK metabolism probably depends on the route of exposure, and is very similar to that of n-hexane. The critical organ is the nervous system. These effects find expression as peripheral neuropathy, with potential for serious effects of the central nervous system. From the viewpoint of neurotoxicity, 2,5-hexanedione is the most important metabolite. The neurotoxicity is potentiated by several compounds, while MBK itself potentiates the toxicity of other chemicals. From animal experiments, a no-adverse-effect level (NAEL) could not be established. Peripheral neuropathy may develop in workers exposed to only a few ppm of MBK. The difference in the Occupational Exposure Limits for MBK and n-hexane, as established by several organizations, is questioned in view of the neurotoxic effects of these substances.
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Authors | P M Bos, G de Mik, P C Bragt |
Journal | American journal of industrial medicine
(Am J Ind Med)
Vol. 20
Issue 2
Pg. 175-94
( 1991)
ISSN: 0271-3586 [Print] United States |
PMID | 1659188
(Publication Type: Journal Article, Research Support, Non-U.S. Gov't, Review)
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Chemical References |
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Topics |
- Animals
- Drug Interactions
- Environmental Monitoring
- Humans
- Methyl n-Butyl Ketone
(adverse effects)
- Occupational Diseases
(chemically induced)
- Occupational Exposure
(adverse effects)
- Peripheral Nervous System Diseases
(chemically induced)
- Risk Factors
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