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Journal of Pharmacology And Experimental Therapeutics, Vol. 94, Issue 4, 401-411, 1948
Copyright © 1948 by American Society for Pharmacology and Experimental Therapeutics


BROMAL HYDRATE AND CHLORAL HYDRATE: A PHARMACOLOGICAL CONTRAST AND ITS CHEMICAL BASIS

THOMAS C. BUTLER 1

1 Department of Pharmacology and Experimental Therapeutics, The Johns Hopkins University, Baltimore, Maryland

1. When bromal hydrate is administered to dogs, neither tribromoethanol nor tribromoacetic acid can be demonstrated in the plasma.

2. Under physiological conditions in vitro bromal hydrate reacts rapidly with serum albumin and with cysteine, the latter substance being oxidized to cystine.

3. It is suggested that the "positive halogen" properties of bromal hydrate are responsible for its high toxicity.

4. The structural features responsible for the difference in reactivity of bromal hydrate and chloral hydrate are discussed.

Submitted on August 20, 1948







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Copyright © 1948 by the American Society for Pharmacology and Experimental Therapeutics.