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  2. Mancozeb - Wikipedia

    en.wikipedia.org/wiki/Mancozeb

    Mancozeb is a dithiocarbamate non-systemic agricultural fungicide with multi-site, protective action on contact. It is a combination of two other dithiocarbamates: maneb and zineb . [ 1 ] The mixture controls many fungal diseases in a wide range of field crops, fruits, nuts, vegetables, and ornamentals.

  3. Metalaxyl - Wikipedia

    en.wikipedia.org/wiki/Metalaxyl

    Metalaxyl is an acylalanine fungicide with systemic function. [3] Its chemical name is methyl N-(methoxyacetyl)-N-(2,6-xylyl)-DL-alaninate. It can be used to control Pythium in a number of vegetable crops, and Phytophthora in peas.

  4. List of fungicides - Wikipedia

    en.wikipedia.org/wiki/List_of_fungicides

    This is a list of fungicides.These are chemical compounds which have been registered as agricultural fungicides.The names on the list are the ISO common name for the active ingredient which is formulated into the branded product sold to end-users. [1]

  5. File:Mancozeb.svg - Wikipedia

    en.wikipedia.org/wiki/File:Mancozeb.svg

    Main page; Contents; Current events; Random article; About Wikipedia; Contact us; Pages for logged out editors learn more

  6. Toxicity label - Wikipedia

    en.wikipedia.org/wiki/Toxicity_label

    Toxicity labels [1] viz; red label, yellow label, blue label and green label are mandatory labels employed on pesticide containers in India identifying the level of toxicity (that is, the toxicity class) of the contained pesticide. [1] [2] [3] The schemes follows from the Insecticides Act of 1968 [1] and the Insecticides Rules of 1971.

  7. Zineb - Wikipedia

    en.wikipedia.org/wiki/Zineb

    Mancozeb - A common fungicide containing Zineb and Maneb. References External links. Zineb in the Pesticide Properties DataBase (PPDB) This page was last ...

  8. Azoxystrobin - Wikipedia

    en.wikipedia.org/wiki/Azoxystrobin

    The first synthesis of azoxystrobin was disclosed in patents filed by the ICI group. [13] The sequence of the two substitution reactions allows for the synthesis of a diverse range of structural analogs via an Ullmann-type etherification between the aryl chloride of the first intermediate and a substituted phenol, thus introducing a range of structural diversity while maintaining the central ...

  9. Carbendazim - Wikipedia

    en.wikipedia.org/wiki/Carbendazim

    High doses of carbendazim destroy the testicles of laboratory animals. [6] [7]Maximum pesticide residue limits (MRLs) for fresh produce in the EU are between 0.1 and 0.7 mg/kg with the exception of loquat fruits, which is set at 2 mg/kg. [8]

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