Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Formation of Cyanide Ion or Cyanogen Chloride through the Cleavage of Aromatic Rings by Nitrous Acid or Chlorine. VII. On the Reaction of Aromatic Amino Acids with Hypochlorous Acid in the Presence of Ammonium Ion
大谷 武司菅野 三郎
著者情報
キーワード: hypochlorous acid
ジャーナル フリー

1984 年 32 巻 1 号 p. 280-283

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抄録
Cyanogen chloride was formed by the reactions of aromatic amino acids such as phenylalanine, tyrosine, tryptophan and histidine with hypochlorous acid in the presence of ammonium ion. It was found that the formation of cyanogen chloride was due to cleavage of the aromatic rings of the aromatic amino acids by chloramine.
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© The Pharmaceutical Society of Japan
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