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  2. Cypermethrin - Wikipedia

    en.wikipedia.org/wiki/Cypermethrin

    Cypermethrin is a broad-spectrum insecticide, which means it kills beneficial insects as well as the targeted insects. [14] Fish are particularly susceptible to cypermethrin, [ 15 ] [ 16 ] but when used as directed, application around residential sites poses little risk to aquatic life. [ 17 ]

  3. Dieldrin - Wikipedia

    en.wikipedia.org/wiki/Dieldrin

    Dieldrin was an insecticide used on fruit, soil, and seed. It persists in the soil with a half-life of five years at temperate latitudes. Both aldrin and dieldrin may be volatilized from sediment and redistributed by air currents, contaminating areas far from their sources.

  4. Diazinon - Wikipedia

    en.wikipedia.org/wiki/Diazinon

    Diazinon is a contact insecticide which kills insects by altering normal neurotransmission within the nervous system of the insect. As mentioned above, diazinon inhibits the enzyme acetylcholinesterase (AChE), which hydrolyzes the neurotransmitter acetylcholine (ACh) in cholinergic synapses and neuromuscular junctions .

  5. Getting the Bugs Out: 22 Cheap, Natural Ways to Rid ... - AOL

    www.aol.com/22-cheap-natural-ways-rid-111300325.html

    Fleas, spiders, termites, flies, centipedes, ants, bedbugs, cockroaches — these icky intruders won't give up. But keeping them away doesn't require expensive chemical pesticides.

  6. Boric acid - Wikipedia

    en.wikipedia.org/wiki/Boric_acid

    Boric acid has also been widely used in the treatment of wood for protection against termites. The full complexity of its mechanism is not fully understood, but aside from causing dose-dependent mortality, boric acid causes dysbiosis in the Eastern Subterranean termite , leading to the opportunistic rise of insect pathogens that could be ...

  7. Carbaryl - Wikipedia

    en.wikipedia.org/wiki/Carbaryl

    Carbaryl is often inexpensively produced by direct reaction of methyl isocyanate with 1-naphthol. [5]C 10 H 7 OH + CH 3 NCO → C 10 H 7 OC(O)NHCH 3. Alternatively, 1-naphthol can be treated with excess phosgene to produce 1-naphthyl chloroformate, which is then converted to carbaryl by reaction with methylamine. [5]

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