Making Waves: Formulation components used in agriculture may serve as important precursors for nitrogenous
Jean M Brownell1, Moshan Chen1, Kimberly M Parker1
1Department of Energy, Environmental & Chemical Engineering, Washington University in St. Louis, St. Louis, Missouri 63130, United States.
Abstract:
N-Nitrosamines, many of which are carcinogenic, mutagenic, and teratogenic, are disinfection byproducts (DBPs) formed from the reaction of chloramine with nitrogenous organic compounds during water disinfection. The identification of major nitrosamine precursors is important to understand and prevent nitrosamine formation. In this analysis, we propose that efforts to identify nitrosamine precursors must look beyond conventionally evaluated active agent chemicals to consider inert or inactive chemicals as potentially relevant precursors. Using agricultural chemicals applied in the US as an example, we demonstrate that amines widely used as inactive agents in herbicide formulations (i.e., dimethylamine [DMA], a known N-nitrosamine precursor) are potentially much more important than active agent herbicides previously evaluated as potential nitrosamine precursors (i.e., the herbicides diuron or trifluralin). Accounting for use rates and nitrosamine yields, amines used in herbicide formulations represent potential nitrosamine precursor inputs to the environment that are similar in magnitude to recognized precursors like the pharmaceuticals ranitidine and metformin. Because the amounts of amines used as inert agents in herbicide formulations have increased dramatically over recent decades, particularly in certain US regions, we suggest that identification of potential nitrosamine precursors should consider variation in the inputs of both active and inactive agents over time, as well as geographical variation in use that may alter the relative importance of specific precursors in certain locations.
More Related Videos
Related Concept Videos
Overview of Nitrogen Metabolism
The largest pool of nitrogen available in the terrestrial ecosystem is gaseous nitrogen (N2) from the air, but this...
2° Amines to N-Nitrosamines: Reaction with NaNO2
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Overview
The nitrous acid is unstable. Hence, it is formed in situ from a solution of sodium nitrite and cold aqueous acids such as hydrochloric or sulfuric acid. In an acidic solution, the –OH group of nitrous acid undergoes protonation to give oxonium ion, followed by...
The Nitrogen Cycle
Diazonium Group Substitution: –OH and –H
1° Amines to Diazonium or Aryldiazonium Salts: Diazotization with NaNO2 Mechanism


