By Wilfried Paulus (Editor)
This version is split into elements. half One provides commonly assorted contributions from 23 international specialists, on such issues as: Microbicides with reference to the connection among chemical constitution and mode of motion and job; learn and improvement in attention of registration systems; Legislative facets. using microbicides in 18 significant program components are defined intimately. half collects Microbicide info, equipped into 21 substance periods (e.g. alcohols, aldehydes, acids, amides, etc.), and together with a few three hundred entries.
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Additional info for Directory of Microbicides for the Protection of Materials and Processes
Journal of Appl. Bacteriology 64, 265. Lewis, S. , Miller, G. , Hausman, M. and Szamborski, E. , 1971. Isothiazoles: 4-Isothiazolinones. A general synthesis from 3,3‘-dithiopropionamides. Journal of Heterocyclic Chemistry 8, 571–580. Lucken, R. , 1966. The fungitoxicity of compounds containing a trichloromethylthio group. J. Agricult. Food Chem. 14, 365–367. Ludwig, R. A. and Thorn, G. , 1960. Chemistry and mode of action of dithiocarbamate fungicides. Ado. Pest. Cont. Res. 3, 219–252. Miller, G.
Today, there is pressure on some bactericides due to environmental concerns and human health hazard and only three points of discussion should be briefly mentioned here. First, the use of bactericides containing chlorine or bromine in the molecule is discussed in Europe because of AOX problems in waste water treatment. Second, there is an increasing pressure on bactericides based on formaldehyde or formaldehyde releasing compounds due to health hazards. The third issue is the R43 labeling (sensitizing through skin contact possible) of products which contain more than 15 ppm CMIT/MIT in a three to one ratio in Europe.
Presents an active ingredient which in contrast to Fluorfolpet is not thermostable, but substantially soluble in non-polar solvents; it is therefore used successfully for the fungicidal and algaecidal treatment of solvent based paints including antifouling coatings and non-film-forming decorative wood stains. Figure 14 Formation of a N-haloalkylthio compounds containing an activated N-S bond. 18 directory of microbicides for the protection of materials Table 2 Antimicrobial activity of R-S-CX3 compounds produced from substances with H atoms of different reactivity.