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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 .

  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. Dilution ratio - Wikipedia

    en.wikipedia.org/wiki/Dilution_ratio

    The following formulas can be used to calculate the volumes of solute (V solute) and solvent (V solvent) to be used: [1] = = where V total is the desired total volume, and F is the desired dilution factor number (the number in the position of F if expressed as "1/F dilution factor" or "xF dilution"). However, some solutions and mixtures take up ...

  5. Diazinon - Wikipedia

    en.wikipedia.org/wiki/Diazinon

    According to the German Patent bureau, the industrial synthesis of diazinon is as follows: β-isobutyrylaminocrotonic acid amine was cyclized with NaOR (R is either a hydrogen or aliphatic chain of 1 to 8 carbons) in a mixture of 0 to 100% by weight of water and an alcohol having 1 to 8 carbon atoms, above 90°C (but below the boiling point of the mixture used).

  6. Chlorothalonil - Wikipedia

    en.wikipedia.org/wiki/Chlorothalonil

    Chlorothalonil (2,4,5,6-tetrachloroisophthalonitrile) is an organic compound mainly used as a broad spectrum, nonsystemic fungicide, with other uses as a wood protectant, pesticide, acaricide, and to control mold, mildew, bacteria, algae. [2] Chlorothalonil-containing products are sold under the names Bravo, Echo, and Daconil.

  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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