Pesticides examples

Mechanism of action can be an important factor determining selectivity. In the extreme case, one group of organisms has a site of action that is not present in another group. Thus, most of the insecticides that are neurotoxic have very little phytotoxicity indeed, some of them (e.g., the OPs dimethoate, disyston, and demeton-5 -methyl) are good systemic insecticides. Most herbicides that act upon photosynthesis (e.g., triaz-ines and substituted ureas) have very low toxicity to animals (Table 2.7). The resistance of certain strains of insects to insecticides is due to their possessing a mutant form of the site of action, which is insensitive to the pesticide. Examples include certain strains of housefly with knockdown resistance (mutant form of Na+ channel that is insensitive to DDT and pyrethroids) and strains of several species of insects that are resistant to OPs because they have mutant forms of acetylcholinesterase. These... 

Example Four Component Pesticide Example. Cornell (2) presented the analysis of a four component pesticide mixture containing Vendex (Xj), Omite, Kelthane (X,), and Dibrom (X.) to control mites on plants. The response, the average percentage of mites seven days... 

Inorganic arsenicals find limited use as pesticides. Examples include arsenious oxide in cattle dips, zinc arsenite as a wood preservative, and calcium and lead arsenates and Paris green (double salt of copper arsenite and copper acetate) as insecticides30. ... 

These activities have enabled WHOPES to plan for the expansion of the Scheme to include the testing and evaluation of a greater variety of pesticides. In recent years, WHOPES has also vigorously promoted the use of WHO specifications for public health pesticides in accordance with the International Code of Conduct on Distribution and Use of Pesticides. Examples of such efforts include the development and wide distribution of guidelines for the purchase of pesticides for public health use, provision of access to WHO specifications for pesticides and their test methods on the Internet, and an increase in the number of WHO collaborating centres for quality control of pesticides (currently three). 

Figures 9 and 10 describe a similar pesticide example based.on the Stauffer Chemical series of thiolcarbamate herbicides. The implied optimum in transport or binding is...

Nature of This Study. The following represents preliminary results of an initial study on the adsorptive behavior of two organometal-llcs. Numerous organometalllcs comprise the active ingredient of various pesticides. Examples include phenylmercurlc salts, diphenyl mercury, triphenyl, tributyl, and tricyclohexyltin salts, as well as organoarsenic compounds (Table 1). Because of the toxicity of these substances their behavior and associations in natural water systems is a matter of concern. 

Dichlorobenzene (DCB) in mothballs provides a different type of pesticide example. A cancer bioassay conducted by NTP (1987) found excess tumors in both rats and mice. The Intemational Agency for Research on Cancer (lARC) concluded that DCB is reasonably anticipated to be a human carcinogen, and it is listed by the State of California as a chemical known to cause cancer (see below). DCB in mothballs results in low vapor levels in areas where it is used, and vapors emanate from clothes worn after storage with DCB. An estimated human inhalation cancer risk value is available (OEHHA, 2005). Despite the widespread exposure and recognized cancer risk, there are no restrictions on the use of DCB for this purpose. 

Most organisms, regardless of complexity, share a number of biochemical pathways for metabolizing pesticides. Examples can... 

Two examples from the analysis of water samples illustrate how a separation and preconcentration can be accomplished simultaneously. In the gas chromatographic analysis for organophosphorous pesticides in environmental waters, the analytes in a 1000-mL sample may be separated from their aqueous matrix by a solid-phase extraction using 15 mb of ethyl acetate. After the extraction, the analytes are present in the ethyl acetate at a concentration that is 67 times greater than that in... 

This publication provides several examples of the use of solid-phase extractions for separating analytes from their matrices. Some of the examples included are caffeine from coffee, polyaromatic hydrocarbons from water, parabens from cosmetics, chlorinated pesticides from water, and steroids from hydrocortisone creams. Extracted analytes maybe determined quantitatively by gas (GC) or liquid chromatography (LG). 

Examples of the application of HPLC to the analysis of (a) acetaminophen, salicylic acid, and caffeine (b) chlorinated pesticides (c) tricyclic antidepressants and (d) peptides. (Chromatograms courtesy of Alltech Associates, Inc. Deerfield, IL). 

The value of many chemical products, from pesticides to pharmaceuticals to high performance polymers, is based on unique properties of a particular isomer from which the product is ultimately derived. Eor example, trisubstituted aromatics may have as many as 10 possible geometric isomers whose ratio ia the mixture is determined by equiHbrium. Often the purity requirement for the desired product iacludes an upper limit on the content of one or more of the other isomers. This separation problem is a compHcated one, but one ia which adsorptive separation processes offer the greatest chances for success. 

Aerosol products are hermetically sealed, ensuring that the contents caimot leak, spill, or be contaminated. The packages can be considered to be tamper-proof. They deUver the product in an efficient manner generating Httie waste, often to sites of difficult access. By control of particle size, spray pattern, and volume deUvered per second, the product can be appHed directiy without contact by the user. For example, use of aerosol pesticides can minimize user exposure and aerosol first-aid products can soothe without applying painful pressure to a wound. Spray contact lens solutions can be appHed directiy and aerosol lubricants (qv) can be used on machinery in operation. Some preparations, such as stable foams, can only be packaged as aerosols. 

These chemorational techniques have generated great interest in, and high expectations for, the acceleration of development of innovative pesticides. However, many purportedly successful appHcations of QSAR procedures have reHed on the quaHtative insights traditionally associated with art-based pesticide development programs. Retrospective QSAR analyses have, however, been helpful in identifying the best compounds for specific uses (17). Chemorational techniques have also found some appHcations in the development of pesticides from natural product lead compounds, the best known examples being the synthetic pyrethroid insecticides (19) modeled on the plant natural product, pyrethmm. 

Substances other than enzymes can be immobilized. Examples include the fixing of heparin on polytetrafluoroethylene with the aid of PEI (424), the controUed release of pesticides which are bound to PEI (425), and the inhibition of herbicide suspensions by addition of PEI (426). The uptake of anionic dyes by fabric or paper is improved if the paper is first catonized with PEI (427). In addition, PEI is able to absorb odorizing substances such as fatty acids and aldehydes. Because of its high molecular weight, PEI can be used in cosmetics and body care products, as weU as in industrial elimination of odors, such as the improvement of ambient air quaHty in sewage treatment plants (428). 

MIBK is a highly effective separating agent for metals from solutions of their salts and is used in the mining industries to extract plutonium from uranium, niobium from tantalum, and zirconium from hafnium (112,113). MIBK is also used in the production of specialty surfactants for inks (qv), paints, and pesticide formulations, examples of which are 2,4,7,9-tetramethyl-5-decyn-4,7-diol and its ethoxylated adduct. Other appHcations include as a solvent for adhesives and wax/oil separation (114), in leather (qv) finishing, textile coating, and as a denaturant for ethanol formulations. 

Methyl- and dimethylnaphthalenes are contained in coke-oven tar and in certain petroleum fractions in significant amounts. A typical high temperature coke-oven coal tar, for example, contains ca 3 wt % of combined methyl- and dimethylnaphthalenes (6). In the United States, separation of individual isomers is seldom attempted instead a methylnaphtha1 ene-rich fraction is produced for commercial purposes. Such mixtures are used for solvents for pesticides, sulfur, and various aromatic compounds. They also can be used as low freezing, stable heat-transfer fluids. Mixtures that are rich in monomethyinaphthalene content have been used as dye carriers (qv) for color intensification in the dyeing of synthetic fibers, eg, polyester. They also are used as the feedstock to make naphthalene in dealkylation processes. PhthaUc anhydride also can be made from m ethyl n aph th al en e mixtures by an oxidation process that is similar to that used for naphthalene. 

The group of tests that must be performed for each pesticide depends on how that pesticide is to be used. For example, if a pesticide is not used on food or feed crops, extensive residue and metaboHsm tests in plants and domestic animals might not be required. Similarly, if a pesticide is not used in field crops nor on other extensive outdoor areas, aH the environmental fate studies might not be required. 

When illegal residues have been found in monitoring studies conducted by the FDA or USD A, the reason has often been that no U.S. tolerance had been requested for that particular pesticide in that specific crop. For example, an imported crop would be deemed to be adulterated and would be seized at the port of entry into the United States if found to contain a pesticide residue in the absence of a tolerance in that crop. This is so even if tolerances have been set for the same pesticide in several crops grown in the United States and the pesticide had been used to control a pest that does not exist in the United States. Furthermore, an international maximum residue level (MRL) might already have been estabUshed for that pesticide—crop combination under the Codex system of standards for food of importance in international trade. The U.S. GAO issued two reports on food safety and pesticides in 1991 (89,90). 

Oxidative Reactions. The majority of pesticides, or pesticide products, are susceptible to some form of attack by oxidative enzymes. For more persistent pesticides, oxidation is frequently the primary mode of metaboHsm, although there are important exceptions, eg, DDT. For less persistent pesticides, oxidation may play a relatively minor role, or be the first reaction ia a metaboHc pathway. Oxidation generally results ia degradation of the parent molecule. However, attack by certain oxidative enzymes (phenol oxidases) can result ia the condensation or polymerization of the parent molecules this phenomenon is referred to as oxidative coupling (16). Examples of some important oxidative reactions are ether cleavage, alkyl-hydroxylation, aryl-hydroxylation, AJ-dealkylation, and sulfoxidation. 

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