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Mercury compounds with fungicidal properties

Organic mercury compounds are discussed in three main groups, according to the nature of the hydrocarbon or substituted hydrocarbon radical. [Pg.284]

Organic mercury compounds containing an alkyl group with a low carbon atom number are classed in this group. The fungicidal effect of the derivatives decreases with increasing carbon atom number (Gassner, 1951), so that, in practice, only methyl- and ethylmercury compounds are important. [Pg.284]

Several methods of preparation have been developed, among them the following  [Pg.284]

Using anhydrous tetrahydrofurane as solvent, the chloride derivatives, slightly soluble in ether, can also be prepared directly (Coates, 1960). Alkylation can also be undertaken with tetraethyl lead compounds (Whelen, 1959). [Pg.284]

The presence of peracetic acid facilitates this reaction (Kloes et al., 1963). [Pg.284]


See other pages where Mercury compounds with fungicidal properties is mentioned: [Pg.283]    [Pg.283]    [Pg.398]    [Pg.2584]    [Pg.398]    [Pg.283]    [Pg.2583]   


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Compound, compounds properties

Compounds (Mercurials)

Fungicidal compounds

Fungicidal properties

Mercurial compounds

Mercury compounds

Mercury properties

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