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  2. Amitraz - Wikipedia

    en.wikipedia.org/wiki/Amitraz

    Amitraz (development code BTS27419) is a non-systemic acaricide and insecticide [1] and has also been described as a scabicide. It was first synthesized by the Boots Co. in England in 1969. [2] Amitraz has been found to have an insect repellent effect, works as an insecticide and also as a pesticide synergist. [3]

  3. White oil - Wikipedia

    en.wikipedia.org/wiki/White_oil

    White oil is an insecticide spray used for controlling a wide range of insect pests in the garden. The spray works by blocking the breathing pores of insects, causing suffocation and death. It is effective in the control of aphids, scale, mealybug, mites, citrus leafminer and other smooth skinned caterpillars. [1] "

  4. Bifenthrin - Wikipedia

    en.wikipedia.org/wiki/Bifenthrin

    Bifenthrin is poorly soluble in water and often remains in soil. Its residual half-life in soil is between 7 days and 8 months, depending on the soil type, with a low mobility in most soil types. Bifenthrin has the longest known residual time in soil of insecticides currently on the market. It is a white, waxy solid with a faint sweet smell.

  5. Acaricide - Wikipedia

    en.wikipedia.org/wiki/Acaricide

    Dicofol, a compound structurally related to the insecticide DDT, is a miticide that is effective against the red spider mite Tetranychus urticae. Lime sulfur is effective against sarcoptic mange. It is made by mixing hydrated lime, sulfur, and water, and boiling for about 1 hour.

  6. Phosmet - Wikipedia

    en.wikipedia.org/wiki/Phosmet

    Phosmet is a phthalimide-derived, non-systemic, organophosphate insecticide used on plants and animals. It is mainly used on apple trees for control of codling moth, though it is also used on a wide range of fruit crops, ornamentals, and vines for the control of aphids, suckers, [clarification needed] mites, and fruit flies.

  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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