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  2. Flufenoxuron - Wikipedia

    en.wikipedia.org/wiki/Flufenoxuron

    Flufenoxuron is an insecticide that belongs to the benzoylurea chitin synthesis inhibitor group, which also includes diflubenzuron, triflumuron, and lufenuron. [1] Flufenoxuron is a white crystalline powder. It is insoluble in water, is not flammable, and is not an oxidizer.

  3. List of insecticides - Wikipedia

    en.wikipedia.org/wiki/List_of_insecticides

    The 2024 IRAC poster of insecticide modes of action includes the majority of chemicals listed below. [5] The pesticide manual provides much information on pesticides. [6] [7] Many of the insecticides in the list are not in use.

  4. 4-Hydroxy-TEMPO - Wikipedia

    en.wikipedia.org/wiki/4-Hydroxy-TEMPO

    4-Hydroxy-TEMPO or TEMPOL, formally 4-hydroxy-2,2,6,6-tetramethylpiperidin-1-oxyl, is a heterocyclic compound. Like the related TEMPO , it is used as a catalyst and chemical oxidant by virtue of being a stable aminoxyl radical .

  5. Spirotetramat - Wikipedia

    en.wikipedia.org/wiki/Spirotetramat

    It is a systemic insecticide that penetrates plant leaves when sprayed on. It is ambimobile , being transported both upwards and downwards through vascular bundles . [ 5 ] In plants, it is hydrolyzed to the enol form by cleavage of the central ethoxycarbonyl group .

  6. Indoor residual spraying - Wikipedia

    en.wikipedia.org/wiki/Indoor_residual_spraying

    Indoor residual spraying or IRS is the process of spraying the inside of dwellings with an insecticide to kill mosquitoes that spread malaria. A dilute solution of insecticide is sprayed on the inside walls of certain types of dwellings—those with walls made from porous materials such as mud or wood but not plaster as in city dwellings.

  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]