Literature DB >> 18996563

Unusual products of the aqueous chlorination of atenolol.

Marina DellaGreca1, Maria Rosaria Iesce, Paola Pistillo, Lucio Previtera, Fabio Temussi.   

Abstract

The reaction of the drug atenolol with hypochlorite under conditions that simulate wastewater disinfection was investigated. The pharmaceutical reacted in 1h yielding three products that were separated by chromatographic techniques and characterized by spectroscopic features. Two unusual products 2-(4-(3-(chloro(2-chloropropan-2-yl)amino)-2-hydroxypropoxy)phenyl) acetamide and 2-(4-(3-formamido-2-hydroxypropoxy)phenyl) acetamide were obtained along with 2-(4-hydroxyphenyl) acetamide. When the reaction was stopped at shorter times only 2-(4-(3-amino-2-hydroxypropoxy)phenyl) acetamide and the dichlorinated product were detected. Tests performed on the seeds of Lactuca sativa show that chlorinated products have phytotoxic activity.

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Year:  2008        PMID: 18996563     DOI: 10.1016/j.chemosphere.2008.09.067

Source DB:  PubMed          Journal:  Chemosphere        ISSN: 0045-6535            Impact factor:   7.086


  2 in total

1.  Graphene Facilitated Removal of Labetalol in Laccase-ABTS System: Reaction Efficiency, Pathways and Mechanism.

Authors:  Shipeng Dong; Huifang Xiao; Qingguo Huang; Jian Zhang; Liang Mao; Shixiang Gao
Journal:  Sci Rep       Date:  2016-02-19       Impact factor: 4.379

2.  The Fate of Sulfamethazine in Sodium-Hypochlorite-Treated Drinking Water: Monitoring by LC-MS (n) -IT-TOF.

Authors:  Tyler C Melton; Stacy D Brown
Journal:  Int J Med Chem       Date:  2012-05-15
  2 in total

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