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  2. Imidacloprid - Wikipedia

    en.wikipedia.org/wiki/Imidacloprid

    Imidacloprid is one of the most widely used insecticide in the world. [4] [5] [6] Its major uses include: Seed treatment – Imidacloprid is a popular seed treatment insecticide in the world [8] Agriculture – Control of aphids, cane beetles, thrips, [16] stink bugs, locusts, and a variety of other insects that damage crops

  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. Pesticide formulation - Wikipedia

    en.wikipedia.org/wiki/Pesticide_formulation

    By far the most frequently used products are formulations for mixing with water then applying as sprays. Water miscible, older formulations include: EC Emulsifiable concentrate; WP Wettable powder; SL Soluble (liquid) concentrate; SP Soluble powder; Newer, non-powdery formulations with reduced or no use of hazardous solvents and improved ...

  5. Campbell Vaughn: When it comes to insecticides, you ... - AOL

    www.aol.com/campbell-vaughn-comes-insecticides...

    Bugs are quick to develop resistance to pesticides, to be sure to change them regularly to keep them away.

  6. Etofenprox - Wikipedia

    en.wikipedia.org/wiki/Etofenprox

    Etofenprox is a broad-spectrum insecticide which disturbs insect nervous systems following direct contact or ingestion, and which is active against a broad spectrum of pests. It is used in agriculture, horticulture, viticulture, forestry, animal health and public health against many insect pests, for instance Lepidoptera , Hemiptera ...

  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]