ATC Code P03
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ATC Code P03
P03A Ectoparasiticides, including scabicides P03AA Sulfur containing products :P03AA01 Dixanthogen :P03AA02 Potassium polysulfide :P03AA03 Mesulfen :P03AA04 Disulfiram :P03AA05 Thiram :P03AA54 Disulfiram, combinations P03AB Chlorine containing products :P03AB01 Clofenotane :P03AB02 Lindane :P03AB51 Clofenotane, combinations P03AC Pyrethrines, including synthetic compounds :P03AC01 Pyrethrum :P03AC02 Bioallethrin :P03AC03 Phenothrin :P03AC04 Permethrin :P03AC51 Pyrethrum, combinations :P03AC52 Bioallethrin, combinations :P03AC53 Phenothrin, combinations :P03AC54 Permethrin, combinations P03AX Other ectoparasiticides, including scabicides :P03AX01 Benzyl benzoate :P03AX02 Copper oleinate :P03AX03 Malathion :P03AX04 Quassia :P03AX05 Dimeticone :P03AX06 Benzyl alcohol :P03AX07 Abametapir P03B Insecticides and repellents P03BA Pyrethrines :P03BA01 Cyfluthrin :P03BA02 Cypermethrin :P03BA03 Decamethrin :P03BA04 Tetramethrin P03BX Other insecticides and repellents :P03BX01 Di ...
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Dixanthogen
: Structure of diethyl dixanthogen disulfide. Dixanthogen disulfides are a class of organosulfur compounds with the formula . Usually yellow solids, they are the product of the oxidation of xanthate salts. A common derivative is diethyl dixanthogen disulfide. Diisopropyl dixanthogen disulfide is commercially available. They are structurally related to thiuram disulfides. Uses and reactions Diethyl dixanthogen disulfide is a component for froth flotations used, inter alia, for the separation of sulfide minerals like pyrrhotite. Diisopropyl dixanthogen disulfide is a reagent in the synthesis of sulfur heterocycles. Dialkoxy dixanthogen disulfides undergo desulfurization by cyanide to give bis(alkoxythiocarbonyl)sulfides: : Dixanthogens are also ectoparasiticide An ectoparasiticide is an antiparasitic drug used in the treatment of ectoparasitic infestations. These drugs are used to kill the parasites that live on the body surface. Permethrin, sulfur, lindane, dicophane, benzyl be ...
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Quassia
''Quassia'' ( or ) is a plant genus in the family Simaroubaceae. Its size is disputed; some botanists treat it as consisting of only one species, ''Quassia amara'' from tropical South America, while others treat it in a wide circumscription as a pantropical genus containing up to 40 species of trees and shrubs. The genus was named after a former slave from Suriname, Graman Quassi in the eighteenth century. He discovered the medicinal properties of the bark of ''Quassia amara''. Distribution Members of the genus are found in the Tropics throughout the world. Countries and regions where species are native include: Andaman Islands, Angola, Bangladesh, Belize, Benin, Bismarck Archipelago, Borneo, North and Northeast Brazil, Burkina, Cabinda, Cambodia, Cameroon, Central African Republic, Chad, Colombia, Comoros, Congo, Costa Rica, El Salvador, Equatorial Guinea, Gabon, Gambia, Ghana, Guatemala, Guinea, Guinea-Bissau, Gulf of Guinea Islands, Honduras, India, Ivory Coast, Kenya, Laos, L ...
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Etohexadiol
Etohexadiol (or ethohexadiol) is an ectoparasiticide An ectoparasiticide is an antiparasitic drug used in the treatment of ectoparasitic infestations. These drugs are used to kill the parasites that live on the body surface. Permethrin, sulfur, lindane, dicophane, benzyl benzoate, ivermectin and crot .... It was known as the insect repellent "6-12" (Six-twelve), or Rutgers 612. Its use in the U.S. was halted in 1991 after it was shown to cause developmental defects in animals. References Alkanediols Insect repellents {{antiinfective-drug-stub ...
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Dimethylcarbate
Dimethyl carbate is an insect repellent. It can be prepared by the Diels–Alder reaction of dimethyl maleate and cyclopentadiene Cyclopentadiene is an organic compound with the chemical formula, formula C5H6.LeRoy H. Scharpen and Victor W. Laurie (1965): "Structure of cyclopentadiene". ''The Journal of Chemical Physics'', volume 43, issue 8, pages 2765-2766. It is often ab .... References Insect repellents Methyl esters {{antiinfective-drug-stub ...
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Dibutylphthalate
Dibutyl phthalate (DBP) is an organic compound which is commonly used as a plasticizer because of its low toxicity and wide liquid range. With the chemical formula C6H4(CO2C4H9)2, it is a colorless oil, although commercial samples are often yellow.Peter M. Lorz, Friedrich K. Towae, Walter Enke, Rudolf Jäckh, Naresh Bhargava, Wolfgang Hillesheim "Phthalic Acid and Derivatives" in Ullmann's Encyclopedia of Industrial Chemistry, 2007, Wiley-VCH, Weinheim. Production and use DBP is produced by the reaction of ''n''-butanol with phthalic anhydride. DBP is an important plasticizer that enhances the utility of some major engineering plastics, such as PVC. Such modified PVC is widely used in plumbing for carrying sewerage and other corrosive materials. Degradation Hydrolysis of DBP leads to phthalic acid and 1-butanol. Monobutyl phthalate (MBP) is its major metabolite. Biodegradation Biodegradation by microorganisms represents one route for remediation of DBP. For example, ''Entero ...
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Dimethylphthalate
Dimethyl phthalate is an organic compound and phthalate ester. it is a colourless and oily liquid that is soluble in organic solvents, but which is only poorly soluble in water (~4 g/L). It is used in a variety of products and is most commonly used as insect repellent such as ectoparasiticide for mosquitoes and flies for animal livestock. The short-chain or low molecular weight phthalate is also frequently used in consumer products such as cosmetics, ink, soap, household cleaning supplies, etc. Other uses of DMP include solid rocket propellants and plastics. The U.S Environmental Protection Agency has classified Dimethyl phthalate as not classifiable for human carcinogenicity. Its oral LD50 is 4390 to 8200 mg/kg bw/d in rats and the dermal LD50 is 38000 mg/kg bw in rats and more than 4800 mg/kg bw in guinea pigs. Synthesis Dimethyl phthalate is manufactured commercially via the esterification of phthalic anhydride with methanol. The reaction can be catalysed by ...
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Diethyltoluamide
''N'',''N''-Diethyl-''meta''-toluamide, also called DEET () or diethyltoluamide, is the most common active ingredient in insect repellents. It is a slightly yellow oil intended to be applied to the skin or to clothing and provides protection against mosquitoes, flies, ticks, fleas, chiggers, leeches and many biting insects. History DEET was developed in 1944 by Samuel Gertler of the United States Department of Agriculture for use by the United States Army, following its experience of jungle warfare during World War II. It was originally tested as a pesticide on farm fields, and entered military use in 1946 and civilian use in 1957. It was used in Vietnam and Southeast Asia. In its original form, known as "bug juice", the application solution was composed of 75% DEET and 25% ethanol. Later, a new version of the repellent was developed by the U.S. Army and the USDA. This formulation consisted of DEET and a mixture of polymers that extended its release and reduced its evaporation ...
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Tetramethrin
Tetramethrin is a potent synthetic insecticide in the pyrethroid family. It is a white crystalline solid with a melting point of 65-80 °C. The commercial product is a mixture of stereoisomer In stereochemistry, stereoisomerism, or spatial isomerism, is a form of isomerism in which molecules have the same molecular formula and sequence of bonded atoms (constitution), but differ in the three-dimensional orientations of their atoms in ...s. It is commonly used as an insecticide, and affects the insect's nervous system. It is found in many household insecticide products. Tetramethrin has an expected half-life of 12.5-14 days in soil and 13-25 days in water. References External linksPyrethrins and Pyrethroids Fact Sheet - National Pesticide Information Center
* Maleimides
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Decamethrin
Deltamethrin is a pyrethroid ester insecticide. Deltamethrin plays a key role in controlling malaria vectors, and is used in the manufacture of long-lasting insecticidal mosquito nets; however, resistance of mosquitos and bed bugs to deltamethrin has seen a widespread increase. Deltamethrin is toxic to aquatic life, particularly fish. Although generally considered safe to use around humans, it is still neurotoxic. It is an allergen and causes asthma in some people. Usage Deltamethrin is a highly effective insecticide. It is used, among other applications, for the production of long-lasting insecticidal nets (LLINs), which, along with indoor residual spraying (IRS), are the main vector control strategies recommended by the World Health Organization (WHO) for the management of malaria. Deltamethrin plays a key role in controlling malaria vectors, and is used in the manufacture of long-lasting insecticidal mosquito nets. It is used as one of a battery of pyrethroid insecticides in ...
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Cypermethrin
Cypermethrin (CP) is a synthetic pyrethroid used as an insecticide in large-scale commercial agricultural applications as well as in consumer products for domestic purposes. It behaves as a fast-acting neurotoxin in insects. It is easily degraded on soil and plants but can be effective for weeks when applied to indoor inert surfaces. Exposure to sunlight, water and oxygen will accelerate its decomposition. Cypermethrin is highly toxic to fish, bees and aquatic insects, according to the National Pesticides Telecommunications Network (NPTN). It is found in many household ant and cockroach killers, including Raid, Ortho, Combat, ant chalk, and some products of Baygon in Southeast Asia. Uses Cypermethrin is used in agriculture to control ectoparasites which infest cattle, sheep, and poultry. Human exposure Cypermethrin is moderately toxic through skin contact or ingestion. It may cause irritation to the skin and eyes. Symptoms of dermal exposure include numbness, tingling, itching, ...
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Cyfluthrin
Cyfluthrin is a pyrethroid insecticide and common household pesticide. It is a complex organic compound and the commercial product is sold as a mixture of isomers. Like most pyrethroids (MoA 3a), it is highly toxic to fish and invertebrates, but it is far less toxic to humans. It is generally supplied as a 10–25% liquid concentrate for commercial use and is diluted prior to spraying onto agricultural crops and outbuildings. Safety In rats, the s are 500, 800 (oral), and 600 (skin) mg/kg. Excessive exposure can cause nausea, headache, muscle weakness, salivation, shortness of breath and seizures. In humans, it is deactivated by enzymatic hydrolysis to several carboxylic acid metabolites, whose urinary excretion half-lives are in a range of 5–7 hours. Worker exposure to the chemical can be monitored by measurement of the urinary metabolites, while severe overdosage may be confirmed by quantification of cyfluthrin in blood or plasma. Health and safety risks are controlled by r ...
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