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Identification of different products obtained by electrochemical and photochemical reduction of the herbicide metamitron

✍ Scribed by Carlos Olmedo; Luis Deban; Enrique Barrado; Yolanda Castrillejo; Luis Herrero


Publisher
Elsevier Science
Year
1994
Tongue
English
Weight
391 KB
Volume
39
Category
Article
ISSN
0013-4686

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✦ Synopsis


The electrochemical reduction of the herbicide Metamitron (4-amino_4,5dihydro-3-methyl& phenyl-1,2,4-triazin-5-one) has been carried out at different pHs using a mercury pool cathode. The iinal product of these reductions depends both on the electrolysis potential and on the pH. All processes are irreversible and the reductions of the C-N and the N-NH, (pH > 3) or N-NH: bond @H < 3) are inferred.

An aqueous solution of Metamitron is also degraded by sunlight leading to 4,5dihydro-3-methyl&phenyl-1,2,4-triazin-5-one (deaminometamitron). This reaction can be monitored polarographically.


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Unsymmetrical disulphides and trisulphides were obtained after electrochemical reduction of 1,2-dithiole-3-thiones in N,N dimethylformamide as by-products in addition to the major symmetrical disulphide. In a previous paper', we reported the electrochemical reduction of 1,2-dithiole-3-thiones