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  2. Bifenthrin - Wikipedia

    en.wikipedia.org/wiki/Bifenthrin

    Products containing bifenthrin include Sevin, Transport, Talstar, Maxxthor, Biforce, Capture, Brigade, Bifenthrine, DuoCide insect control, Ortho Home Defense Max, Bifen XTS, Bifen IT, Bifen L/P, Torant, Zipak, Scotts Turf Builder SummerGuard, Wisdom TC Flowable, FMC 54800, Allectus, Ortho Max Pro and OMS3024 and mega wash from green planet and ...

  3. Scotts Miracle-Gro Company - Wikipedia

    en.wikipedia.org/wiki/Scotts_Miracle-Gro_Company

    The company manufactures and sells consumer lawn, garden and pest control products, as well as soilless indoor gardening equipment. [3] In the U.S., the company manufactures Scotts, Miracle-Gro and Ortho brands. It also markets and distributes the herbicide Roundup in the U.S. and several international markets including China. [4]

  4. Chlordane - Wikipedia

    en.wikipedia.org/wiki/Chlordane

    In the years 1948–1988 chlordane was a common pesticide for corn and citrus crops, as well as a method of home termite control. [6] Pathways of exposure to chlordane include ingestion of crops grown in chlordane-contaminated soil, inhalation of air in chlordane-treated homes and from landfills, and ingestion of high-fat foods such as meat ...

  5. The Best Time To Apply Weed Killer To A Lawn, According To ...

    www.aol.com/best-time-apply-weed-killer...

    Before you opt for a chemical weed killer, consider alternatives that are less damaging to the environment, garden, lawn, and your wallet. Better yet, dedicate time to managing your lawn and fewer ...

  6. Monroe County agriculture: Birkey offers tips for healthy ...

    www.aol.com/monroe-county-agriculture-birkey...

    Monroe County agriculture: Birkey offers tips for healthy lawns, insect control. Gannett. Ned Birkey. July 2, 2024 at 3:30 AM.

  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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