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  2. S-Ethyl dipropylthiocarbamate - Wikipedia

    en.wikipedia.org/wiki/S-Ethyl_dipropylthiocarbamate

    S-Ethyl dipropylthiocarbamate (EPTC) is a selective herbicide used for pre-emergent control of certain grasses and broadleaf weeds in Australia and the United States. [3] [4] It was introduced in 1957. [5] EPTC can be applied pre-emergently or post-emergently and its effectiveness does not depend on post-application rainfall.

  3. Pesticide formulation - Wikipedia

    en.wikipedia.org/wiki/Pesticide_formulation

    By far the most frequently used products are formulations for mixing with water then applying as sprays. Water miscible, older formulations include: EC Emulsifiable concentrate; WP Wettable powder; SL Soluble (liquid) concentrate; SP Soluble powder; Newer, non-powdery formulations with reduced or no use of hazardous solvents and improved ...

  4. Nufarm - Wikipedia

    en.wikipedia.org/wiki/Nufarm

    Nufarm is listed on the Australian Stock Exchange (symbol NUF) and its head office is located at Laverton in Melbourne. [2] As at close on Friday 4 October 2019, its ordinary share capital was valued at AUD$6.49, implying a market capitalisation of AUD$2.45 billion.

  5. Glyphosate-based herbicides - Wikipedia

    en.wikipedia.org/wiki/Glyphosate-based_herbicides

    Roundup was the first glyphosate-based herbicide, developed by Monsanto in the 1970s. It is used most heavily on corn, soy, and cotton crops that have been genetically modified to be resistant to the herbicide. Some products include two active ingredients, such as Enlist Duo which includes 2,4-D as well as glyphosate. As of 2010, more than 750 ...

  6. Glyphosate - Wikipedia

    en.wikipedia.org/wiki/Glyphosate

    Glyphosate has four ionizable sites, with pKa values of 2.0, 2.6, 5.6 and 10.6. [83] Therefore, it is a zwitterion in aqueous solutions and is expected to exist almost entirely in zwitterionic forms in the environment. Zwitterions generally adsorb more strongly to soils containing organic carbon and clay than their neutral counterparts. [84]

  7. Butafenacil - Wikipedia

    en.wikipedia.org/wiki/Butafenacil

    By 1993 a patent claiming specific ester derivatives including butafenacil was published. [6] This was developed for the market under the code number CGA276854 and launched in 2001. [ 1 ] [ 7 ] By that time, further mergers in the industry meant that the product was supplied by Syngenta [ 8 ] with brand names including B Power.

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