Systemic Fungicide

Fenbuconazole Fenfuram Fenpropimorph Flutriafol Fosetyl-aluminum 8-Hydroxyquinoline sulfate Imazalil Oxycarboxin Tebuconazole Thiophanate Triadimenol Tridemorph fungicide, systemic agric. 

CioHgC NOiS. A protective non-systemic fungicide used principally for the control of potato blight. M.p. 160-161 C. It is relatively non-toxic to most animal life although it is harmful to hsh. 

Copper electrodes Copper foil Copper fungicides Copper glycinate Copper-gold Copper halide Copper halide system... 

Microtubulin Polymerization Inhibitors. The ben2imida2oles were first reported to have systemic fungicidal activity in 1964 (29). Prominent examples include thiabendazole [148-79-8] (42) fuberida2ole [3878-19-1] (43) carbendazim [10605-21-7] (44) benomyl [17804-35-2] (45) and thiophanate methyl [23564-05-8] (46). Benomyl (45), the most widely used member of this group is almost certainly inactive as a fungicide until it is converted in plants and soil to carbendazim (44). Likewise, thiophanate and thiophanate methyl (46) are nonfungitoxic until converted to carbendazin (44). 

Pesticide Solvent. The majority of organic fungicides, insecticides, and herbicides (qv) are soluble in DMSO, including such difficult-to-solvate materials as the substituted ureas and carbamates (see Fungicides, agricultural Insect control technology Pesticides). Dimethyl sulfoxide forms cosolvent systems of enhanced solubiUty properties with many solvents (109). 

More recently, self-assembling 3//-azepine monolayers on a gold surface have been obtained by the photodecomposition of bis ll-[(4-azidobenzoyl)oxy]undec-l-yl disulfide.284 Other than some alkyl and aryl 177-azepine-l-carboxylates, which possess fungicidal activity, particularly against Sclerotium rolfsii,104 the unsaturated azepine systems surveyed in this section do not have any notable biological activity. 

The rapid rise in the industrial (catalyst in PVC and foam production), agricultural (fungicides and acaricides), and biological applications (wood, stone, and glass preservatives) of organotin(IV) compounds during the last few decades has led to their accumulation in the environment and, consequently, in biological systems. 

A method has been reported for the quantification of five fungicides (shown in Figure 5.39) used to control post-harvest decay in citrus fruits to ensure that unacceptable levels of these are not present in fruit entering the food chain [26]. A survey of the literature showed that previously [27] APCl and electrospray ionization (ESI) had been compared for the analysis of ten pesticides, including two of the five of interest, i.e. carbendazim and thiabendazole, and since it was found that APCl was more sensitive for some of these and had direct flow rate compatibility with the HPLC system being used, APCl was chosen as the basis for method development. 

Organometallic compounds such as alkylmercury fungicides, and tetraethyl lead, used as an antiknock in petrol, are neurotoxic, especially to the central nervous system of vertebrates (Wolfe et al. 1998, Environmental Health Criteria 101, and Chapter 8,... 

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