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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. 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]

4. 2,4-Dichlorophenoxyacetic acid - Wikipedia

   en.wikipedia.org/wiki/2,4-Dichlorophenoxyacetic_acid

   2,4-Dichlorophenoxyacetic acid is an organic compound with the chemical formula Cl 2 C 6 H 3 OCH 2 CO 2 H.It is usually referred to by its ISO common name 2,4-D. [4] It is a systemic herbicide that kills most broadleaf weeds by causing uncontrolled growth, but most grasses such as cereals, lawn turf, and grassland are relatively unaffected.

5. 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:

6. Dilution ratio - Wikipedia

   en.wikipedia.org/wiki/Dilution_ratio

   For example, in a solution with a 1:5 dilution ratio, entails combining 1 unit volume of solute (the material to be diluted) with 5 unit volumes of the solvent to give 6 total units of total volume. In photographic development, dilutions are normally given in a '1+x' format.

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]