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  2. Pesticide formulation - Wikipedia

    en.wikipedia.org/wiki/Pesticide_formulation

    The biological activity of a pesticide, be it chemical or biological in nature, is determined by its active ingredient (AI - also called the active substance). Pesticide products very rarely consist of the pure active ingredient. The AI is usually formulated with other materials (adjuvents and co-formulants) and this is the product as sold, but ...

  3. Mixing ratio - Wikipedia

    en.wikipedia.org/wiki/Mixing_Ratio

    Two binary solutions of different compositions or even two pure components can be mixed with various mixing ratios by masses, moles, or volumes. The mass fraction of the resulting solution from mixing solutions with masses m 1 and m 2 and mass fractions w 1 and w 2 is given by:

  4. White oil - Wikipedia

    en.wikipedia.org/wiki/White_oil

    Concentrates must be diluted before use at a ratio of 10–20 ml concentrate per litre of water and placed in a spray bottle or sprayer. [13] [10] [9] As with ready-to-use spray bottles or cans, the mixture is applied to all surfaces of a plant's leaves and stems. [8] [9] [10] [11]

  5. Chlordane - Wikipedia

    en.wikipedia.org/wiki/Chlordane

    Chlordane, or chlordan, is an organochlorine compound that was used as a pesticide. It is a white solid. In the United States, chlordane was used for termite-treatment of approximately 30 million homes until it was banned in 1988. [4] Chlordane was banned 10 years earlier for food crops like corn and citrus, and on lawns and domestic gardens. [5]

  6. Chlorpyrifos - Wikipedia

    en.wikipedia.org/wiki/Chlorpyrifos

    Chlorpyrifos is normally supplied as a 23.5% or 50% liquid concentrate. The recommended concentration for direct-spray pin point application is 0.5% and for wide area application a 0.03–0.12% mix is recommended (US). [25] [26]

  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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