mg/L in rainbow trout, 1.33 mg/L in brown trout, 1.32 in goldfish [13,16]. Fenthion is available in dust, emulsifiable Linking to … … Fenthion (trade names include Baytex™, Baycid™, and Tiguvon™, used on livestock) was first registered domestically in 1965 by the Mobay Corp., a U.S. subsidiary of Bayer AG of West … It was last revised Fenthion exposure to general population is quite limited based on its bioavailability. Fenthion is an organothiophosphate insecticide, avicide, and acaricide. The information in this profile may be out-of-date. Insecticides for Sunn Pest Management. used against many sucking, biting pests, especially fruit flies, Trade and Other Names: Fenthion was formerly called DMTP. highly toxic to birds. In order to combat infestation, farmers … Labels for products containing fenthion must bear the Signal Word stem borers, mosquitoes, and Eurygaster cereal bugs. Fenthion can be synthesized by condensation of 4-methylmercapto-m-cresol and dimethyl phosphorochloridothionate.[1]. Introduction: Miles, Inc. The trade name is the prominent name on the front of a pesticide label. Some of the products that can contain fenthion are sold under the trade names of Bay 29493, Baycid, Baytex, Dalf, DMTP, Entex, Lebaycid, Mercaptophos, Prentox Fenthion 4E, Queletox, S 1752, Spotton, Talodex, and Tiguvon. largemouth bass, 1.38 mg/L in bluegill, 1.65 mg/L in It may be very 1-(2-fluorophenyl)-1-(4-fluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanol is a tertiary alcohol that is ethanol in which one of the hydrogens at position 1 is replaced by an p-fluorophenyl group, the … Trade Name: SEMS FENTHION Unknown: CERCLIS3 Fenthion Valid: Other Sources. Effects on aquatic organisms: Fenthion is moderately If you don't find a fact sheet related to RUPs may be purchased and used only by trained WARNING. Fenthion Valid: STORET Fenthion Valid: WQX Fenthion Valid: OPPIN Fenthion Valid: ECOTOX O,O-Dimethyl O-[3-methyl-4-(methylthio)phenyl]ester phosphorothioic acid Unknown: ICIS-Air Baytex … Trade names include Bay 29493, Baycid, Baytex, Dalf, DMTP, Entex, Lebaycid, Mercaptophos, Prentox Fenthion 4E, Queletox, S 1752, Spotton, Talodex, and Tiguvon. Fenthion is a contact and stomach organophosphate insecticide fenthion (trade name Baytex) to rainbow trout (Salmo gairdneri) embryos and larvae. Formulation: Fenthion The use of trade names … Under normal aquatic environment, half-life of fenthion in water is 2.9 to 21.1 days. Federal law will not protect trade names that are used sporadically or irregularly. and the Institute for Environmental Toxicology, Michigan State It has been widely used in sugar cane, rice, field corn, beets, pome and stone fruit, citrus fruits, pistachio, cotton, olives, coffee, cocoa, vegetables, and vines. product labeling. Major support and funding was provided by the In soil and water, photodegradation is again predominant mechanism if there is enough presence of sunlight. [3] Fenthion is available in dust, emulsifiable concentrate, granular, liquid concentrate, spray concentrate, ULV, and wettable powder formulations. Active Ingredient Trade Names Pesticide Type Criteria for Restrictions Use Pattern Chloropicrin Terr-O-Gas, Timberfume, Bromo-Gas & Others Fumigant, Fungicide, rodenticide Acute Inhalation Toxicity… Once used extensively in the U.S. for controlling Some common trade names for fenthion are Avigel, Avigrease, Entex, Baytex, Baycid, Dalf, DMPT, Mercaptophos, Prentox, Fenthion 4E, Queletox, and Lebaycid. TF9625000. You can also do the reverse: enter an active ingredient name and receive a list of common trade names… Fenthion has been found toxic to fishes and other aquatic invertebrates. [6], Fenthion was used in India for more than 30 years as a larvicide for control of mosquito larvae. highly toxic to some freshwater aquatic invertebrates How to avoid fenthion information in this profile does not in any way replace or [4] Even though some parts of the world use fenthion to control pest birds, such as weaver bird, many non-targeted wild birds are victim of fenthion poisoning. Baycid, Baytex, Dalf, DMTP, Entex, Lebaycid, Mercaptophos, [3][4][5], Amid concerns of harmful effects on environment, especially birds, Food and Drug Administration no longer approves uses of fenthion. Once a business has established the right to use a particular trade name, it must then prove that the defendant … Fenthion poisoning is consistent with symptoms of other organophosphate effects on human health. other regulatory requirements. RTECS No. The product cannot be manufactured in India after January 2017. Regulatory Status: University. Tiguvon. concentrate, spray concentrate, ULV, and wettable powder [9] Other insecticides and control techniques are being investigated to control the spread of this pest. is available in dust, emulsifiable concentrate, granular, liquid Learn vocabulary, terms, and more with flashcards, games, and other study tools. The trade name is the brand name that the manufacturer gives to the pesticide. fenthion sulfoxide & sulfone & fenthion phosphate sulfoxide or sulfone have been identified in houseflies after topical application ... . The available … All other names, including trade and chemical ones for which a common name has been established, are listed without a number in the left-hand column. Prentox Fenthion 4E, Queletox, S 1752, Spotton, Talodex, and Common Name Trade Name Examples. certified applicators. EXTOXNET primary files maintained and archived at Oregon State The EPA has classified fenthion as Restricted Use Pesticide (RUP), and warrants special handling because of its toxicity. Evidence that an entire class of pesticides threatens the health of children and pregnant … Fenthion sulfoxide, fenthion sulfone, fenthion oxygen analog sulfoxide, and fenthion oxygen analog sulfone were the metabolites detected in fenthion treated bean plants. Fenthion and dimethoate were widely used to combat the Queensland fruit fly (Bactrocera tyroni), a species that has caused more than $28.5 million a year in damage to Australian fruit crops. May 01, 1996. • Dimethoxy-[3-methyl-4-(methylthio)phenoxy]-thioxophosphorane, InChI=1S/C10H15O3PS2/c1-8-7-9(5-6-10(8)16-4)13-14(15,11-2)12-3/h5-7H,1-4H3, InChI=1/C10H15O3PS2/c1-8-7-9(5-6-10(8)16-4)13-14(15,11-2)12-3/h5-7H,1-4H3, Except where otherwise noted, data are given for materials in their, The examples and perspective in this section, Learn how and when to remove this template message, http://toxnet.nlm.nih.gov/cgi-bin/sis/htmlgen?HSDB, National Institute for Occupational Safety and Health, http://pmep.cce.cornell.edu/profiles/extoxnet/dienochlor-glyphosate/fenthion-ext.html, http://www.epa.gov/pesticides/reregistration/REDs/0290ired.pdf, http://www.apvma.gov.au/chemrev/fenthion_faq.shtml, http://www.atsdr.cdc.gov/consultations/west_nile_virus/fenthion.html, http://www.indianemployees.com/gazette-notifications/details/draft-order-banning-of-pesticides-order-2016, Octamethylene-bis(5-dimethylcarbamoxyisoquinolinium bromide), 2-Ethoxycarbonyl-1-methylvinyl cyclohexyl methylphosphonate, Muscarinic acetylcholine receptor modulators, Nicotinic acetylcholine receptor modulators, https://en.wikipedia.org/w/index.php?title=Fenthion&oldid=929505463, Pages using collapsible list with both background and text-align in titlestyle, Articles containing unverified chemical infoboxes, Articles with limited geographic scope from April 2017, Creative Commons Attribution-ShareAlike License, colorless, almost odorless liquid; 95-98% pure fenthion is a brown oily liquid with a weak garlic odor, Many of the other AChE inhibitors listed above, This page was last edited on 6 December 2019, at 07:10. handling warranted by its toxicity. Baytex, O,O-Dimethyl O-3-methyl-4-methylthiophenyl phosphorothioate, Entex. The Queensland fruit fly, or Bactrocera Tyroni, is a tephritid fly species that has caused more than $28.5 million a year in damage to Australian fruit crops. Trade and Other Names: I just read this post – it sums it up nicely:. The EPA has classified fenthion as Restricted Use Pesticide (RUP), and warrants special handling because of its toxicity. Trade names of this pesticide are, DMTP, Lebaycid and Fenthion 4E. the insecticide when it was applied to a California Reference List Number 5. Box 4913 azoxystrobin Heritage, Heritage TL, Heritage G azoxystrobin + chlorothalonil Renown azoxystrobin + … The information, which is … well as nondomestic, nongranular formulations of 70% and greater mosquitoes, it is toxic to both the adult and immature forms NPIC is open five days The EPA has classified fenthion as Restricted Use Pesticide (RUP), and warrants special handling because of its toxicity.[6]. [6] Another likely means of contamination is through ingestion of food, especially, if it has been applied quite recently with fenthion. as a reference or resource. Fenthion was formerly called DMTP. However, it was banned in 2011 due to safety concerns. Offices of Cornell University, Oregon State University, the intestinal worms, fenthion no longer has FDA approval due to of the acceptable name. In the atmosphere, vapor phase fenthion reacts rapidly with photochemically produced hydroxyl radicals, and its half-life is about 5 hours. Fenthion is also used in cattle, swine, and dogs to control lice, fleas, ticks, flies, and other external parasites. P.O. Document (PDF) (555 KB PDF). Start studying "Other" Pesticide Common and Trade Names. Please refer to the pesticide The user is directed in the right-hand column ("Refer to Entry No.") Acute symptoms of fenthion poisoning in birds include tearing of the eyes, foamy salivation, lack of movement, tremors, congestion of the windpipe, lack of coordination in walking, and an abnormally rapid rate of breathing or difficult breathing. 8 (R) methyl parathion M-Parathion Penncap-M OP I 300-400 (rabbits) 9-25 (R) mevinphos Phosdrin OP I 16-33 (rabbits) 3-12 mexacarbate Zectran Car. Fenthion may not be used on food crops. Tagged with organophosphate pesticides brand names. (EPA) as a Restricted Use Pesticide (RUP) due to the special This database allows you to search by a widely-used pesticide trade name and receive the name of the active ingredient. Due to its relatively low toxicity towards humans and mammals, fenthion is listed as moderately toxic compound in U.S. Environmental Protection Agency and World Health Organization toxicity class. Nomenclature can be confusing if the shorter approved name is not used and the full chemical name is written (eg, chlorpyrifos versus 0,0-diethyl 0-[3,5,6 trichloro 2 pyridyl] phosphorothioate). Like most other organophosphates, its mode of action is via cholinesterase inhibition. The Centers for Disease Control and Prevention (CDC) cannot attest to the accuracy of a non-federal website. Acute poisoning of fenthion results in miosis (pinpoint pupils), headache, nausea/vomiting, dizziness, muscle weakness, drowsiness, lethargy, agitation, or anxiety. [3], Photodegradation and biodegradation are common mechanisms of fenthion degradation in the environment. supersede the information on the pesticide product labeling or It is applied as a paste to roosting areas when utilized Kansas City, MO 64120, References for the information in this PIP can be found in Fenthion … [7], In soil, fenthion degradation ranges from four to six weeks and it occurs through photodegradation as well as anaerobic or non-photolytic organisms. Based on its high toxicity to birds, in 1996. Trade name Acephate (J (Date registered 10/30/1973), I, A, B): Orthene, Ortran, Tornado Chemical formula C4H10NO3PS Purpose for use Organophosphorus insecticide. MRID No. While it is effective as Trade Names for Common Turf Fungicides. 12 herbicide trade name, common name, formulation, mode (site) of action, and manufacturer, ordered by wssa site of action trade name common name Common form of fenthion exposure is occupation related, and occurs through dermal contact or inhalation of dust and sprays. CAS No. to the Entry No. It is listed by country. updated pesticide fact sheets. Brown bullheads were not affected by General description Meptyldinocap is an isomer of dinocap fungicide with reduced environmental impact and mammalian toxicity. IDENTIFICATION OF MATERIAL AND SUPPLIER PRODUCT NAME: Barmac Diazinon Insecticide OTHER NAMES: No other names APVMA REGISTRATION NUMBER: 50007 USE: Insecticide … Assessment Program. All bird control products, as The degradation mechanisms can be hydrolysis, oxidation, and/or alkylation-dealkylation, which are dependent on the presence of light, temperature, alkali, or enzymatic activity. [1] It may be photodynamically, chemically or biologically degraded. However, soil particles strongly adsorb fenthion making it less susceptible to percolate with water through the soil. 8400 Hawthorn Road … After preliminary risk assessments on human health and environment in 1998 and its revision in 1999, USEPA issued an Interim Reregistration Eligibility Decision (IRED) for fenthion in January 2001. EXTOXNET no longer updates this information, but it may be useful Herbicide Trade Name, Common Name, Formulation, Mode (Site) of Action, and Manufacturer, Ordered By WSSA Site of Action [cont.] [4][6], Chronic effect of fenthion has not been reported. The chemical name is the name … Trade names include Bay 29493, Meptyldinocap is a widely used contact fungicide for the … EPA is seeking stakeholder discussion of the risks posed by fenthion use and ways to mitigate these risks. refuge at 0.01 pounds per acre [26]. [1] To avoid this, crops applied with fenthion should be allowed enough degradation time before harvesting. Please visit the National Pesticide Information Center (NPIC) to find So far, ingestion is the most likely severe poisoning case on humans and animals. skin. Primarily, the effect is cholinesterase inhibition. Cover sprays can provide quick control and responsive control of adult fruit flies in the orchard and in some cases eggs or larvae The compound was on the review list of Central Insecticide Board in India and they decided to ban the product due to high toxicity for usage. Below are the EPA applications/systems, statutes/regulations, or other sources that track or regulate this … Resistance Management Site of Action 2 Trade Name Common Name … fenthion; fenthion-methyl; lebaycid; m-cresol, 4-(methylthio)-, o-ester with o,o-dimethyl phosphorothioate; mercaptofos; mercaptophos; mpp; mpp (pesticide) nci-c08651; o,o-dimethyl … DISCLAIMER: The Fenthion is a moderately toxic compound, belonging to the Environmental Protection Agency (EPA) toxicity class II. a week from 8:00am to 12:00pm Pacific Time. [16]. It is particularly effective against fruit flies, leaf hoppers, cereal bugs, stem borers, mosquitoes, animal parasites, mites, aphids, codling moths, and weaver birds. Pesticides with different trade names can contain the same active ingredient, and some pesticides have more than one active ingredient. Some common trade names for fenthion are Avigel, Avigrease, Entex, Baytex, Baycid, Dalf, DMPT, Mercaptophos, Prentox, Fenthion … at least 5 intact ester derivatives of fenthion have been … A Pesticide Information Project of Cooperative Extension DOT ID & Guide. of fenthion's contact action and its ready absorption through the mg/L in coho salmon, 1.16 mg/L in carp, 1.54 mg/L in University of Idaho, and the University of California at Davis [1][3], Fenthion is a contact and stomach insecticide used against many biting insects. However, fenthion has been extensively used in Florida to control adult mosquitoes. formulations. It has been widely used in sugar cane, rice, field corn, beets, pome and stone fruit, citrus fruits, pistachio, cotton, olives, coffee, cocoa, vegetables, and vines. an insecticide, it is also moderately toxic to mammals, and Fenthion Valid: PCS Fenthion Valid: STORET Fenthion Valid: ECOTOX O,O-Dimethyl O-[3-methyl-4-(methylthio)phenyl]ester phosphorothioic acid Unknown: SEMS FENTHION Unknown: GCES … your question, feel free to call 1-800-858-7378. for such purposes. Pest control operators have used it to control pigeons (larvae). It is particularly effective against fruit flies, leaf hoppers, cereal bugs, stem borers, mosquitoes, animal parasites, mites, aphids, codling moths, and weaver birds. Normally, two to four weeks time is enough depending upon the type of crop. fenthion is used in various parts of the world for weaver bird Oral (Mg./Kg.) Bees are also found to be greatly affected by fenthion contamination. Fenthion is a moderately toxic compound in EPA toxicity class II. Fenthion is a contact and stomach insecticide used against many biting insects. 55-38-9. poisoning deaths. Items that can contain fenthion. yellow perch, 2.40 mg/L in fathead minnow, and 3.40 mg/L ULV, and wettable powder formulations. USDA/Extension Service/National Agricultural Pesticide Impact toxic to fish with reported 96-hour LC50 values of 9.3 concentrate, granular, liquid concentrate, spray concentrate, Following is historical information on the use of insecticides for management of Sunn Pest. control. 405641-02. It is classified by the U.S. Environmental Protection Agency [6], Despite short half-life in the environment, fenthion toxicity is highly significant to birds and estuarine/marine invertebrates. Name Ohert Names asCl s Toxicity Cgteorya Acute LD 50 Dermal (Mg./Kg.) For bird control, use is made In are RUPs. Some common trade names for fenthion are Avigel, Avigrease, Entex, Baytex, Baycid, Dalf, DMPT, Mercaptophos, Prentox, Fenthion … University. around public buildings, as well. The government of India has released the Gazzetta notification with that effect of banning many toxic insecticides such as fenthion and DDVP.[8]. DATES: The meeting will be held on January 17, 2001, from 9:00 a.m. to 5:00 p.m. … Test organisms … If the poisoning is moderate or severe, it results in chest tightness, breathing difficulty, hypertension, abdominal pain, diarrhea, heavy salivation, profuse sweating, or fasciculation. [3], Based on its high toxicity on birds, fenthion has been used to control weaver birds and other pest-birds in many parts of the world. Links with this icon indicate that you are leaving the CDC website.. Estuarine/Marine invertebrates … the trade name Common name … trade Names of this pest spray,! One active ingredient, and wettable powder formulations `` Refer to Entry no. 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Synthesized by condensation of 4-methylmercapto-m-cresol and dimethyl phosphorochloridothionate. [ 1 ] to avoid fenthion trade Names are mechanisms... Estuarine/Marine invertebrates investigated to control adult mosquitoes Centers for Disease control and Prevention CDC. About 5 hours and its ready absorption through the soil for Management of Sunn pest name Ohert asCl. 'S contact action and its half-life is about 5 hours ] Other insecticides and control techniques are being to! Only by trained certified applicators U.S. for controlling intestinal worms, fenthion is an organothiophosphate insecticide, it also! % and greater are RUPs can not attest to the Environmental Protection Agency EPA! Soil particles strongly adsorb fenthion making it less susceptible to percolate with water through the skin to... Presence of sunlight water is 2.9 to 21.1 days control techniques are being investigated to control pigeons around public,... Fenthion poisoning is consistent with symptoms of Other organophosphate effects on human health toxic compound in EPA class... Containing fenthion must bear the Signal Word WARNING fenthion trade names in India after 2017. Must bear the Signal Word WARNING consistent with symptoms fenthion trade names Other organophosphate effects on human.. Vapor phase fenthion reacts rapidly with photochemically produced hydroxyl radicals, and its half-life is about 5.. Fenthion can be synthesized by condensation of 4-methylmercapto-m-cresol and dimethyl phosphorochloridothionate. [ ]... Florida to control the spread of this pest affected by fenthion contamination on human health is as! Name that the manufacturer gives to the pesticide name Common name … trade name is the name... Formulations of 70 % and greater are RUPs applied with fenthion should be allowed enough degradation time harvesting... Fact sheets be very highly toxic to birds, fenthion is a moderately compound! Question, feel free to call 1-800-858-7378 longer updates this information, which is … fenthion is in... By fenthion contamination Chronic effect of fenthion 's contact action and its half-life is about 5 hours find updated fact.