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  2. Diafenthiuron - Wikipedia

    en.wikipedia.org/wiki/Diafenthiuron

    Next to that, the repeated use of diafenthiuron can lead to the development of resistance in target pests, reducing the efficacy of the insecticide over time. Side effects Apart from enzymatic conversion, diafenthiuron readily dissolves in organic solvents or is broken down by sunlight into two major by-products; diafenthiuron carbodiimide and ...

  3. Toxicity label - Wikipedia

    en.wikipedia.org/wiki/Toxicity_label

    Toxicity labels [1] viz; red label, yellow label, blue label and green label are mandatory labels employed on pesticide containers in India identifying the level of toxicity (that is, the toxicity class) of the contained pesticide. [1] [2] [3] The schemes follows from the Insecticides Act of 1968 [1] and the Insecticides Rules of 1971.

  4. Dichlorvos - Wikipedia

    en.wikipedia.org/wiki/Dichlorvos

    Dichlorvos (2,2-dichlorovinyl dimethyl phosphate, commonly abbreviated as an DDVP [1]) is an organophosphate widely used as an insecticide to control household pests, in public health, and protecting stored products from insects. The compound has been commercially available since 1961.

  5. 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.

  6. Federal Insecticide, Fungicide, and Rodenticide Act - Wikipedia

    en.wikipedia.org/wiki/Federal_Insecticide...

    Mexican Brand Insect Fluid, "Under the Insecticide Act of 1910" The Federal Insecticide Act (FIA) of 1910 was the first pesticide legislation enacted. [2] This legislation ensured quality pesticides by protecting farmers and consumers from fraudulent and/or adulterated products by manufacturers and distributors.

  7. Chlorfenapyr - Wikipedia

    en.wikipedia.org/wiki/Chlorfenapyr

    Chlorfenapyr was developed by American Cyanamid from the natural product dioxapyrrolomycin, which was isolated from Streptomyces fumanus. [2]The United States Environmental Protection Agency initially denied registration in 2000 for use on cotton primarily because of concerns that the insecticide was toxic to birds and because effective alternatives were available. [3]

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  9. Pesticide formulation - Wikipedia

    en.wikipedia.org/wiki/Pesticide_formulation

    A particularly efficient form of pesticide dose transfer is seed treatment and specific formulations have been developed for this purpose. A number of pesticide bait formulations are available for rodent pest control, etc.