organophosphate
Sign in to saveAlso known as phosphate ester, organophosphates, phosphate esters, phosphoric ester
thumb|right|General chemical structure of the organophosphate functional group
Research
46,216 papers- Organophosphate pesticide-induced toxicity through DNA damage and DNA repair mechanisms.Molecular biology reports · 2023
- Exploring organophosphate ester contamination and distribution in food: A meta-analysis.Food chemistry · 2024
- Association between exposure to organophosphate esters metabolites and sarcopenia prevalence: A cross-sectional study using NHANES data.Ecotoxicology and environmental safety · 2024
- Organophosphate esters in water and air: A minireview of their sources, occurrence, and air-water exchange.Chemosphere · 2024
- Organophosphate exposure and the chronic effects on farmers: a narrative review.Rural and remote health · 2020
via PubMed
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Encyclopedic overview
21 sectionsContents
- Forms
- Synthesis
- Alcoholysis of {{chem2|POCl3}}
- Esterification of phosphoric acid and P<sub>2</sub>O<sub>5</sub>
- Oxidation of phosphite esters
- Phosphorylation
- Laboratory methods
- Properties
- Bonding
- Acidity
- Water solubility
- Industrial materials
- Pesticides{{anchor|Insecticides}}
- Flame retardants
- Plasticisers
- Hydraulic fluids and lubricant additives
- Metal extractants
- Surfactants
- Nerve agents
- In nature
- References
thumb|right|General chemical structure of the organophosphate functional group
In organic chemistry, organophosphates (also known as phosphate esters, or OPEs) are a class of organophosphorus compounds with the general structure , a central phosphate molecule with alkyl or aromatic substituents. They can be considered as esters of phosphoric acid. Organophosphates are best known for their use as pesticides.
Excerpted from Wikipedia’s “organophosphate” article, available under the CC BY-SA 4.0 licence.