ArticleslgStudy

biology

Malathion

Malathion is a biology topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Malathion rather than just read about it. In short: Malathion is an organophosphate insecticide which acts as an acetylcholinesterase inhibitor. In the USSR, it was known as carbophos, in New Zealand and Australia as maldison and in South Africa as mercaptothion.

Malathion — main illustration
Malathion — illustration

Key takeaways

  • Malathion belongs to biology; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Malathion to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Malathion from memory before moving on to harder problems.

Reference excerpt

Malathion is an organophosphate insecticide which acts as an acetylcholinesterase inhibitor. In the USSR, it was known as carbophos, in New Zealand and Australia as maldison and in South Africa as mercaptothion.

Pesticide use Malathion is a pesticide that is widely used in agriculture, residential landscaping, public recreation areas, and in public health pest control programs such as mosquito eradication. In the US, it is the most commonly used organophosphate insecticide. A malathion mixture with corn syrup was used in the 1980s in Australia to combat the Mediterranean fruit fly. In Canada and the US starting in the early 2000s, malathion was sprayed in many cities to combat west Nile virus. In the United Kingdom, malathion was withdrawn from sale in 2002.

Mechanism of action Malathion is an acetylcholinesterase inhibitor, a diverse family of chemicals. Upon uptake into the target organism, it binds irreversibly to the serine residue in the active catalytic site of the cholinesterase enzyme. The resultant phosphoester group is strongly bound to the cholinesterase, and irreversibly deactivates the enzyme which leads to rapid build-up of acetylcholine at the synapse.

Production method Malathion is produced by the addition of dimethyl dithiophosphoric acid to diethyl maleate or diethyl fumarate in the presence of catalytic amounts of triethylamine and hydroquinone at elevated temperature:

(CH3O)2PS2H + C8H12O4 → C10H19O6PS2 This process produces the S enantiomer.

Medical use Malathion in low doses (0.5% preparations) is used as a treatment for head lice and body lice infection (pediculosis) in the US, where it is approved by the US Food and Drug Administration. In some areas in the UK, head lice had developed a resistance to malathion as of 1999, and it was ineffective against 64% of cases. This is believed to be caused by development in the lice of an enzyme-mediated malathion specific esterase, able to destroy malathion bound to the acetylcholine receptor. It is also used for the treatment of scabies. Preparations include Derbac-M, Prioderm, Quellada-M and Ovide.

Risks

General Malathion is of low toxicity. In arthropods it is metabolized into malaoxon which is 61 times more toxic, being a more potent inhibitor of acetylcholinesterase. In studies of the effects of long-term exposure to oral ingestion of malaoxon in rats, malaoxon has been shown to be 61 times more toxic than malathion, and malaoxon is 1,000 times more potent than malathion in terms of its acetylcholinesterase inhibition. Absorption or ingestion into the human body also readily results in its metabolism to malaoxon, which is substantially more toxic. It is cleared from the body quickly, in three to five days. According to the United States Environmental Protection Agency, no reliable information is available on adverse health effects of chronic exposure. In 1981, Malathion was sprayed over a 1,400 sq mi (3,600 km2) area to control an outbreak of Mediterranean fruit flies in California. In order to demonstrate the chemical's safety, B. T. Collins, director of the California Conservation Corps, publicly swallowed a mouthful of dilute malathion solution.

Carcinogenicity Malathion is classified by the IARC as probable carcinogen (group 2A). Malathion is classified by US EPA as having "suggestive evidence of carcinogenicity". This classification was based on the occurrence of liver tumors at excessive doses in mice and female rats and the presence of rare oral and nasal tumors in rats that occurred following exposure to very large doses. Exposure to organophosphates is associated with non-Hodgkin's lymphoma. Malathion used as a fumigant was not associated with increased cancer risk. Between 1993 and 1997, as part of the Agricultural Health Study, no clear association between malathion exposure and cancer was reported.

Toxicity to amphibians Malathion is toxic to leopard frog tadpoles.

Regulation Different organizations and governments have set different drinking water quality standards for malathion. The World Health Organization has determined that while malathion can last in water for months and years, it usually does not last in water for longer than one to two weeks; and since the amount of malathion found in drinking water is usually lower than a level that would lead to concerns about health that there is no need to set a drinking water guideline for the level of malathion allowed in water. In contrast, the Canadian government has set a maximum acceptable concentration of 0.29 mg/L of malathion in drinking water, and requires that drinking water should be monitored for the chemical when there is a reason to suspect it is in the water and might need to be removed. Australia has a much lower maximum level of 0.07 mg/L of malathion in drinking water. The European Union has set their level still lower at 0.10 μg/L for any one pesticide in drinking water, including malathion. The United States does not have an official maximum contaminant level for malathion, but proposes a lifetime health advisory of 0.5 mg/L.

See also Isomalathion Pesticide toxicity to bees

References

External links Malathion Technical Fact Sheet - National Pesticide Information Center Malathion General Fact Sheet - National Pesticide Information Center Malathion Pesticide Information Profile - Extension Toxicology Network Malathion in the Pesticide Properties DataBase (PPDB)

Illustrations

Malathion: Structural formula of malathion
Structural formula of malathion
Malathion: 3D representation of malathion
3D representation of malathion
Malathion: Space filling model of malathion, showing van der Waals radii for each atom
Space filling model of malathion, showing van der Waals radii for each atom
Malathion illustration
Malathion illustration

Worked examples

Example 1 — a first encounter with Malathion

Start with the simplest possible case. Write down what Malathion claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In biology, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Malathion before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Malathion ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Malathion

In research
Malathion appears in biology research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Malathion in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Malathion is common in secondary-school and first-year university syllabi. It links to neighbouring topics Acetylcholinesterase inhibitors, Antiparasitic agents, Ethyl esters, so understanding it makes those chapters shorter.
In everyday life
Look for Malathion outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
Ask Teacher Smith questions about this articleOpens your AI tutor with a question about “Malathion” →

Affiliate

Preply — study more efficiently by working with a personal tutor. 50% off.

How to study Malathion in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Malathion means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Malathion out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Malathion in simple terms?

Malathion is an organophosphate insecticide which acts as an acetylcholinesterase inhibitor. In the USSR, it was known as carbophos, in New Zealand and Australia as maldison and in South Africa as mercaptothion.

Why does Malathion matter?

Because it connects several biology ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Malathion?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Malathion.

Tags

  • Acetylcholinesterase inhibitors
  • Antiparasitic agents
  • Ethyl esters
  • IARC Group 2A carcinogens
  • Neurotoxins
  • Organophosphate insecticides
  • Phosphorodithioates

Keep exploring