1.
Chemosphere
; 145: 464-9, 2016 Feb.
Artigo
em Inglês
| MEDLINE
| ID: mdl-26694797
RESUMO
Reaction of 2-aminophenol (2AP) with monochloramine in aqueous solution was investigated at pH 8.5 and 25 °C, with an excess of monochloramine. 2-Amino-3H-phenoxazin-3-one (APO) was the major product formed in about 70% yield. Despite low formation yields, adsorbable organic halides (AOX) were also formed over reaction time.