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  2. Malathion - Wikipedia

    en.wikipedia.org/wiki/Malathion

    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 .

  3. Propoxur - Wikipedia

    en.wikipedia.org/wiki/Propoxur

    Propoxur (Baygon) is a carbamate non-systemic insecticide, produced from catechol, [2] and was introduced in 1959. It has a fast knockdown and long residual effect, and is used against turf, forestry, and household pests and fleas. It is also used in pest control for domestic animals, Anopheles mosquitoes, ants, gypsy moths, and other ...

  4. Benzyl benzoate - Wikipedia

    en.wikipedia.org/wiki/Benzyl_benzoate

    Benzyl benzoate is an organic compound which is used as a medication and insect repellent. [1] As a medication it is used to treat scabies and lice. [2] For scabies either permethrin or malathion is typically preferred. [3] It is applied to the skin as a lotion. [2] Typically two to three applications are needed. [2]

  5. Flea treatments - Wikipedia

    en.wikipedia.org/wiki/Flea_treatments

    A spot-on insecticide kills the fleas on the pet. A fogger or spray insecticide containing an insect growth regulator, such as pyriproxyfen or methoprene can kill eggs and pupae, which are quite resistant to insecticides. A comparison of 3 insecticides (selamectin, fipronil, imidacloprid) showed that selamectin reduced larval cat fleas ≥93.5% ...

  6. 1989 California medfly attack - Wikipedia

    en.wikipedia.org/wiki/1989_California_medfly_attack

    It was instead ordered that, rather than 1–2 aerial sprayings of the infected communities, more than a dozen sprayings would be necessary over a period of months. [19] In addition, Malathion was no longer used alone, but mixed in a 4:1 ratio with Nu-Lure0 bait to attract insects to the area.

  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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