Chlorpyrifos: Difference between revisions
mNo edit summary |
CSV import |
||
| Line 1: | Line 1: | ||
= | {{Short description|Organophosphate pesticide used in agriculture}} | ||
{{Use dmy dates|date=October 2023}} | |||
{{Pesticide}} | |||
[[File:Industrial synthesis of chlorpyrifos.svg|thumb|Industrial synthesis of chlorpyrifos]] | |||
Chlorpyrifos | [[File:Chlorpyrifos USA 2011.png|thumb|Chlorpyrifos usage in the USA, 2011]] | ||
[[File:Chlorpyrifos-oxon.svg|thumb|Chemical structure of chlorpyrifos-oxon, a metabolite of chlorpyrifos]] | |||
'''Chlorpyrifos''' is an organophosphate pesticide widely used in agriculture to control a variety of pests. It was first introduced in 1965 by Dow Chemical Company and has been used on crops such as corn, soybeans, fruit trees, and vegetables. Chlorpyrifos acts on the nervous system of insects by inhibiting the enzyme acetylcholinesterase, leading to the accumulation of acetylcholine and subsequent paralysis and death of the pest. | |||
Chlorpyrifos is | |||
== | ==Chemical Properties== | ||
Chlorpyrifos is | Chlorpyrifos is a crystalline solid with a molecular formula of C<sub>9</sub>H<sub>11</sub>Cl<sub>3</sub>NO<sub>3</sub>PS. It is moderately soluble in water and has a low vapor pressure, which limits its volatility. The compound is stable under normal conditions but can degrade in the presence of sunlight and alkaline conditions. | ||
==Mechanism of Action== | |||
Chlorpyrifos exerts its toxic effects by inhibiting acetylcholinesterase, an enzyme essential for the breakdown of acetylcholine in the synaptic cleft. This inhibition leads to an accumulation of acetylcholine, resulting in continuous stimulation of muscles, glands, and central nervous system structures, ultimately causing paralysis and death in insects. | |||
== | ==Uses== | ||
Chlorpyrifos is used in agriculture to control a wide range of pests, including: | |||
* | * Aphids | ||
* | * Caterpillars | ||
* Beetles | |||
* Mites | |||
It is applied in various forms, including sprays, granules, and seed treatments. The pesticide is also used in non-agricultural settings, such as golf courses and turf management. | |||
== | ==Health and Environmental Concerns== | ||
Chlorpyrifos has been associated with potential health risks to humans, particularly in children and agricultural workers. Exposure can occur through inhalation, skin contact, or ingestion of residues on food. Health effects may include: | |||
* Neurological symptoms such as headaches, dizziness, and confusion | |||
* Developmental delays in children | |||
* Respiratory issues | |||
Environmental concerns include its potential to contaminate water sources and its toxicity to non-target organisms, such as birds, fish, and beneficial insects. | |||
== | ==Regulation and Controversy== | ||
The use of chlorpyrifos has been subject to regulatory scrutiny and controversy. In the United States, the Environmental Protection Agency (EPA) has taken steps to restrict its use due to health concerns. Several countries have banned or severely restricted chlorpyrifos, while others continue to allow its use under specific conditions. | |||
[[ | ==Also see== | ||
[[ | * [[Organophosphate poisoning]] | ||
[[ | * [[Pesticide regulation]] | ||
* [[Acetylcholinesterase inhibitor]] | |||
* [[Environmental impact of pesticides]] | |||
==References== | |||
{{Reflist}} | |||
[[Category:Organophosphate insecticides]] | |||
[[Category:Agricultural chemicals]] | |||
[[Category:Neurotoxins]] | |||
Latest revision as of 02:45, 11 December 2024
Organophosphate pesticide used in agriculture



Chlorpyrifos is an organophosphate pesticide widely used in agriculture to control a variety of pests. It was first introduced in 1965 by Dow Chemical Company and has been used on crops such as corn, soybeans, fruit trees, and vegetables. Chlorpyrifos acts on the nervous system of insects by inhibiting the enzyme acetylcholinesterase, leading to the accumulation of acetylcholine and subsequent paralysis and death of the pest.
Chemical Properties[edit]
Chlorpyrifos is a crystalline solid with a molecular formula of C9H11Cl3NO3PS. It is moderately soluble in water and has a low vapor pressure, which limits its volatility. The compound is stable under normal conditions but can degrade in the presence of sunlight and alkaline conditions.
Mechanism of Action[edit]
Chlorpyrifos exerts its toxic effects by inhibiting acetylcholinesterase, an enzyme essential for the breakdown of acetylcholine in the synaptic cleft. This inhibition leads to an accumulation of acetylcholine, resulting in continuous stimulation of muscles, glands, and central nervous system structures, ultimately causing paralysis and death in insects.
Uses[edit]
Chlorpyrifos is used in agriculture to control a wide range of pests, including:
- Aphids
- Caterpillars
- Beetles
- Mites
It is applied in various forms, including sprays, granules, and seed treatments. The pesticide is also used in non-agricultural settings, such as golf courses and turf management.
Health and Environmental Concerns[edit]
Chlorpyrifos has been associated with potential health risks to humans, particularly in children and agricultural workers. Exposure can occur through inhalation, skin contact, or ingestion of residues on food. Health effects may include:
- Neurological symptoms such as headaches, dizziness, and confusion
- Developmental delays in children
- Respiratory issues
Environmental concerns include its potential to contaminate water sources and its toxicity to non-target organisms, such as birds, fish, and beneficial insects.
Regulation and Controversy[edit]
The use of chlorpyrifos has been subject to regulatory scrutiny and controversy. In the United States, the Environmental Protection Agency (EPA) has taken steps to restrict its use due to health concerns. Several countries have banned or severely restricted chlorpyrifos, while others continue to allow its use under specific conditions.
Also see[edit]
- Organophosphate poisoning
- Pesticide regulation
- Acetylcholinesterase inhibitor
- Environmental impact of pesticides
References[edit]
<references group="" responsive="1"></references>