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article · Proceedings of the National Academy of Sciences

Unexpected formation of oxygen-free products and nitrous acid from the ozonolysis of the neonicotinoid nitenpyram

202033 citationsOpen accessDebre Berhan University

In plain language

The neonicotinoid pesticide nitenpyram is widely applied in agricultural operations and for flea management in domestic animals. When exposed to atmospheric pollutants such as ozone, the substance undergoes oxidation, creating new chemical derivatives that possess toxicological profiles distinct from the parent compound. Analysis of the ozonolysis process reveals that several resulting breakdown products do not contain oxygen, despite developing within an intensely oxidising chemical environment. Furthermore, this degradation pathway releases nitrous acid, which serves as a major precursor to reactive hydroxyl free radicals in the air. Documenting this unusual reaction mechanism is essential for accurately mapping the atmospheric lifetime, degradation pathways, and broader environmental impacts of nitenpyram.

Key takeaways

  • Nitenpyram reacts with atmospheric ozone to produce breakdown products with toxicities distinct from the parent pesticide.
  • Multiple ozonolysis products lack oxygen despite forming within a highly oxidising setting.
  • The reaction between ozone and nitenpyram generates nitrous acid, a notable source of atmospheric hydroxyl radicals.
  • Understanding these newly identified reaction mechanisms is vital for assessing the environmental fate and impact of the compound.

Why it matters

Pesticides interact continuously with air pollutants, generating secondary compounds that behave unpredictably in the environment. Demonstrating that nitenpyram breaks down into unexpected, oxygen-free substances and generates airborne nitrous acid enables environmental scientists and regulators to properly assess the true ecological and atmospheric consequences of widespread agricultural and veterinary chemical use.

Commercialisation angle

This is early-stage research focused on fundamental reaction pathways rather than a direct commercial technology. The findings could eventually be utilised by environmental regulators, ecotoxicologists, and agrochemical manufacturers to refine environmental impact assessments and safety data for pesticide registrations. Any direct application remains far from market, as the findings serve primarily to improve chemical hazard modelling and atmospheric monitoring protocols.

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Abstract

Significance The neonicotinoid nitenpyram (NPM) has widespread use in agricultural settings and for flea control in animals. This may be oxidized on contact with air pollutants such as ozone to form new products that have different toxicity compared to the parent compound, yet little is known of the reaction kinetics, products, and mechanisms. We show here that many of the ozonolysis products of NPM do not contain oxygen, despite the highly oxidizing environment. Understanding such unusual and previously unrecognized chemistry is critical for accurate assessment of the environmental fates and impacts of this neonicotinoid. We also show that nitrous acid, a major source of the highly reactive hydroxyl free radical in air (but whose sources are controversial), is also generated.

Research topics

  • Insect and Pesticide Research
  • Molecular Junctions and Nanostructures
  • Spectroscopy and Quantum Chemical Studies

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DOI: 10.1073/pnas.2002397117

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