Paper

Formation of cyanide ion or cyanogen chloride through the cleavage of aromatic rings by nitrous acid or chlorine. IX. On the reactions of chlorinated, nitrated, carboxylated or methylated benzene derivatives with hypochlorous acid in the presence of ammonium ion

Published Jan 1, 1987 · N. Maeda, T. Ohya, K. Nojima

Chemosphere

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Abstract

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Study Snapshot

Chlorinated, nitrated, carboxylated, or methylated benzene derivatives react with hypochlorous acid to produce cyanogen chloride, with 2,4,6-trichlorophenol yielding 13.3% cyanogen chloride.

PopulationOlder adults (50-71 years)

Sample size24

MethodsObservational

OutcomesBody Mass Index projections

ResultsSocial networks mitigate obesity in older groups.

Formation of cyanide ion or cyanogen chloride through the cleavage of aromatic rings by nitrous acid or chlorine. IX. On the reactions of chlorinated, nitrated, carboxylated or methylated benzene derivatives with hypochlorous acid in the presence of ammonium ion

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