Chlorantraniliprole belongs to the IRAC chemical group 28: Diamides (Ryanodine receptor modulators). Molecular Formula C 18 H 14 BrCl 2 N 5 O 2; Average mass 483.146 Da; Monoisotopic mass 480.970795 Da; ChemSpider ID 9446648; More details: Systematic name . « l'ouverture anarchique des canaux ioniques (les récepteurs à la ryanodine, RyR), qui sont responsables de la libération de, « des effets débilitants qui se traduisent notamment par des déficits locomoteurs durables (plus de 24h). 3-Bromo-1- (3-chloro-2-pyridinyl)- N - [4-cyano-2-methyl-6- (methylcarbamoyl)phenyl]-1 H -pyrazole-5-carboxamide. Send us your requirement details of chlorantraniliprole 95%TC 2 Chemical Class: Anthranilic diamide insecticide Mode of Action: Interruption of normal muscle contraction Pesticide Type: Insecticide U.S. Technical Registrant: DuPont Crop Protection P.O. Coragen Chlorantraniliprole 3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide 28 Dupont Co-Ral Coumaphos O,O-diethyl O-(3-chloro-4-methyl-2-oxo2H-1-enzopyuran 7-yl- phosphorothioate 1B Bayer Corporation Co-Ral Plus Coumpahos + Diazinon Cette altération de la régulation musculaire épuise les réserves de calcium présent dans les fibres musculaires et conduit à la paralysie, puis à la mort de l'insecte[3]. New class of chemistry Anthralinic Diamides group: 16. In 2018–19 Australia exported 205 kt of sorghum grain valued at $95.8 million (ABARES estimate . CHICKPEA, MUNG BEAN, SOYBEAN: DO NOT GRAZE OR CUT FOR STOCK FOOD FOR 14 DAYS AFTER APPLICATION Son mode d'action consiste à surstimuler les muscles des insectes en déclenchant l'activation des récepteurs de ryanodine. A ryanodine receptor agonist, it is used as insecticide for the con trol of whitefly, thrips, aphids, fruitflies, and fruit worms in crops such as onions, potatoes and tomatoes. Chlorantraniliprole (CAS No. [1] Chlorantraniliprole is being developed world-wide by DuPont belonging to a new class of selective insecticides featuring a novel mode of action to control a range of pests belonging to the order Lepidoptera and some other Coleoptera, Diptera and Isoptera species. Names. b. Chlorantraniliprole 18.5% SC having the trade name Coragen. Chlorantraniliprole 18.5% SC : Coragen (DuPont) ~ Effective and long duration control of early and top borer in sugarcane. http://echa.europa.eu/information-on-chemicals/registered-substances Une étude récente (2019), postérieure à son autorisation, a confirmé des symptômes sublétaux et mortels chez l'abeille domestique[2]. Cyantraniliprole. a. Chlorantraniliprole 0.4% GR having the trade name Ferterra. As active ingredient (a.i.) Chlorantraniliprole opens muscular calcium channels (in particular the ryanodine receptor), rapidly causing paralysis and ultimately death of sensitive species. in insecticide -. Subscribe here. 2.2. Common Name: Chlorantraniliprole Experimental Name: DPX-E2Y45 EPA PC Code: 090100 . Chlorantraniliprole is active on chewing pest insects primarily by ingestion and secondarily by contact. Chlorantraniliprole (DPX-E2Y45, Rynaxypyr®,Coragen®) is a new compound by DuPont belonging to a new class of selective insecticides (anthranilic diamides) featuring a novel mode of action (group 28 in the IRAC classification). Preventing the buildup of the pest population. It has been classified as non toxic to birds, mammals, and fish. Chlorantraniliprole acts against a wide range of insects including many species of moths, leafrollers, armyworms, caterpillars, white grubs, and beetles. Chlorantraniliprole | C18H14BrCl2N5O2 | CID 11271640 - structure, chemical names, physical and chemical properties, classification, patents, literature, biological activities, safety/hazards/toxicity information, supplier lists, and more. INSECTICIDE. Chlorantraniliprole 3D molecular model generated using Avogadro software, 5-bromo-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-2-(3-chloropyridin-2-yl)pyrazole-3-carboxamide, InChI=1S/C18H14BrCl2N5O2/c1-9-6-10(20)7-11(17(27)22-2)15(9)24-18(28)13-8-14(19)25-26(13)16-12(21)4-3-5-23-16/h3-8H,1-2H3,(H,22,27)(H,24,28), CC1=C(C(=CC(=C1)Cl)C(=O)NC)NC(=O)C2=CC(=NN2C3=C(C=CC=N3)Cl)Br, Except where otherwise noted, data are given for materials in their, EPA Pesticides Fact Sheet: Chlorantraniliprole, https://en.wikipedia.org/w/index.php?title=Chlorantraniliprole&oldid=977442818, Pages using collapsible list with both background and text-align in titlestyle, Articles containing unverified chemical infoboxes, Articles with unsourced statements from April 2020, Creative Commons Attribution-ShareAlike License, This page was last edited on 8 September 2020, at 21:36. Chlorantraniliprole (trade name Rynaxypyr®, DuPont, Wilmington, DE, USA) is an anthranilic diamide insecticide that binds to ryanodine receptors, resulting in the unregulated release of calcium from insect muscle cells and leading to the cessation of feeding, lethargy, muscle paralysis, and death (Han et al., 2012, Cordova et al., 2006). Il a été approuvé par la commission Européenne malgré les lacunes notamment identifiées par l'EFSA dans son « projet de rapport d'évaluation » (DAR) relatif à ses impacts potentiels sur les pollinisateurs[2]. Chlorantraniliprole (Ref: DPX E2Y45) Last updated: 04/01/2021 (Also known as: rynaxypyr; IN-E2Y45) Cyantraniliprole. Le chlorantraniliprole est une substance active de produit phytosanitaire ; c'est la première molécule de la famille chimique des diamides anthraniliques mise sur le marché, qui présente un puissant effet insecticide et acaricide. Chlorantraniliprole is a very targeted pesticide that has wide variations in effect on non target pests La dernière modification de cette page a été faite le 9 octobre 2020 à 15:27. Depuis l'autorisation de mise sur le marché de ce produit, des études in vitro et des études comportementales faites sur l'abeille domestique ont montré que le chlorantraniliprole induit : Un article de Wikipédia, l'encyclopédie libre. NO. https://fr.wikipedia.org/w/index.php?title=Chlorantraniliprole&oldid=175425910, Substance active de produit phytosanitaire, Portail:Agriculture et agronomie/Articles liés, Portail:Protection des cultures/Articles liés, licence Creative Commons attribution, partage dans les mêmes conditions, comment citer les auteurs et mentionner la licence. Chlorantraniliprole (Acelepryn®; Syngenta, Greensboro, North Carolina, U.S.) is the first anthranilic diamide registered for use on turf- grass and landscape ornamentals. 4. Coragen Chlorantraniliprole 3-bromo-N-[4-chloro-2-methyl-6-[(methylamino)carbonyl]phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxamide 28 Dupont Co-Ral Coumaphos O,O-diethyl O-(3-chloro-4-methyl-2-oxo2H-1-enzopyuran 7-yl- phosphorothioate 1B Bayer Corporation Co-Ral Plus Coumpahos + Diazinon It is very efficient for controlling lepidopteran insect pests, as well as some species in the orders Diptera, Hemiptera, and Coleoptera. Your Email 500008-45-7) is an insecticide that operates by a highly specific biochemical mode of action. WITHHOLDING PERIODS HARVEST COTTON: DO NOT HARVEST FOR 28 DAYS AFTER APPLICATION. Chlorantraniliprole is being developed world-wide by DuPont belonging to a new class of selective insecticides featuring a novel mode of action to control a range of pests belonging to the order Lepidoptera and some other Coleoptera, Diptera and Isoptera species. Chlorantraniliprole 2 Product Results | Match Criteria: Product Name, Description * Acetamiprid 20 SP (S) 0.20 g Yellow Pride,Ekka,Polar,Tata Manik, Lift,Ennova,Judo,Prima,Active. Collet, C., Kadala, P. A., Charreton, M., & Charnet, P. (2019, August). Chlorantraniliprole is a member of the anthranilic diamine class of insecticides.This insecticide affects insect ryanodine receptors, which means it interrupts normal muscle contraction. Coragen (chlorantraniliprole): A diamide that has contact activity, but is most effective through ingestion of treated plant material. IUPAC name. Il a aussi été commercialisé environ respectivement 15, 10 et 9 fois moins que l'imidaclopride, la cyperméthrine et le chlorpyriphos-ethyl (produits alors les plus vendus parmi les insecticides néonicotinoïdes, pyréthrinoïdes et organophosphorés) [2]. USE PATTERNS AND FORMULATIONS … Other names. Malgré une relative rémission à 48h, les abeilles présentent les signes d'une rechute sévère 7 jours après exposition », « la question de la validité des tests OCDE classiques pour évaluer cette nouvelle classe d'insecticides ». Chlorantraniliprole Identification; Nom UICPA: 3-bromo-4′-chloro-1-(3-chloro-2-pyridyl)-2′-methyl-6′-(methylcarbamoyl)pyrazole-5-carboxanilide: N o CAS: N o ECHA: InChI INSECTICIDES AND THEIR COMMERCIAL NAME SL. The differential selectivity Chlorantraniliprole had towards insect ryanodine receptors explained the outstanding profile of low mammalian toxicity[citation needed]. chlorantraniliprole. Chlorantraniliprole (Rynaxypyr) is an insecticide of the ryanoid class. 3-Bromo-N-[4-chloro-2-methyl-6-(methylca rbamoyl)phenyl]-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carbo xamide. Effets débilitants d'un nouvel insecticide avec rechute sévère plusieurs jours après exposition-Perturbation de l'homéostasie calcique neuromusculaire des abeilles et effets topiques différentiels. CHICKPEA, MUNG BEAN, SOYBEAN: DO NOT HARVEST FOR 14 DAYS AFTER APPLICATION GRAZING DO NOT ALLOW LIVESTOCK TO GRAZE CROPS, COTTON STUBBLE OR GIN TRASH TREATED WITH ALTACOR? It is a selective and potent activator of insect ryanodine receptors (RyRs) that are critical for muscle contraction. Aluminiumphosphide 56 Tab 1 Tab(3g) / … SMILES. COMMON TRADE NAMES Exirel, Verimark, Benevia, Fortenza, A17960A, Spinner, A16901B MAJOR DEGRADATES Multiple (13) APPLICATION RATE (lbs a.i./A) Single: 0.04 - 0.4 Max Annual: 0.4 HONEY BEE ICON EPA has registered cyantraniliprole as a broad-spectrum insecticide for Present REGISTRATION STATUS EPA: February 2014 Minnesota: February 2014 TOXICITY PROFILE FOR APPLICATORS Signal … Your Name. Chlorantraniliprole 0.4% GR: Ferterra (DuPont) ~ Preventing the buildup of the pest population. 405 chlorantraniliprole products are offered for sale by suppliers on Alibaba.com, of which insecticide accounts for 15%, animal pharmaceuticals accounts for 3%, and herbicide accounts for 2%. Jump to navigation Jump to search. Chemical Name Dose&Group (ml or g /L) Commercial Name 1. New class of chemistry Anthralinic Diamides group: 17. STAR BIO SCIENCE is leading Manufacturer & Supplier of chlorantraniliprole 95%TC in Kolkata, WB. Insects rapidly stop feeding, become paralyzed and typically die within 1-3 days. 4). contact name company or group name (if relevant) ... chlorantraniliprole. Box 30 Newark, DE 19714-0030 Chemical Structure: N N N NH O Cl Br HN O Cl 2. Chlorantraniliprole is a new reduced risk insecticide by Dupont. Cc1cc(cc(c1NC(=O)c2c c(nn2c3c(cccn3)Cl)Br)C(=O)NC)Cl Copy. A carboxamide that is chlorantraniliprole in which the chlorine atom attached to the phenyl ring has been replaced by a cyano group. It is highly toxic to honeybees. Becomes systemic when applied to soil. Cet insecticide est vendu comme efficace notamment sur les lépidoptères des cultures fruitières et légumières, contre l'eudémis et la cochylis sur la vigne, contre la pyrale du maïs, et contre le doryphore sur pomme de terre, tomate et aubergine. Destination and value of sorghum exports . In 30ème Congrès UIEIS-Insectes Sociaux-Section Française. Chlorantraniliprole is a novel anthranilic diamide insecticide belonging to the class of selective ryanodine receptor agonists. Std. The mode of action is different to most other commercial insecticides. From Wikipedia, the free encyclopedia. Acephate 75 WP (S) 0.75- 1.50 g Blue Tamaron Gold,Asataf,Lancer, Pace,Dhanraj, 3. InChi. Chlorantraniliprole ( Rynaxypyr) is an insecticide of the ryanoid class. Chlorantraniliprole is the ISO approved common name for 3-bromo-N-[4-chloro-2-methyl-6-(methylcarbamoyl)phenyl]-1-(3-chloropyridin-2-yl)-1H-pyrazole-5-carboxamide). The risk to trade with respect to maize grain and animal commodities is low and does not require further consideration. Ce pesticide (insecticide/acaricide) a rapidement été très utilisé, dont en France ; ainsi en 2016, en a ton vendu en France environ 18 tonnes, soit respectivement ~1.7, 2, 3 et 7 fois plus que la pymétrozine, l'indoxacarbe, le fénoxycarbe et l'émamectine, 4 molécules en tête des ventes pour les familles des pyridines, oxadiazines, carbamates et avermectines)[2]. A wide variety of chlorantraniliprole options are available to you, such as powder, liquid. http://ec.europa.eu/food/plant/pesticides/eu-pesticides-database/public/?event=homepage&language=EN. … Subscribe to the IRAC eConnection to receive our latest news in your inbox. 356 Chlorantraniliprole IN-DBC80 CAS name: 3-Bromo-1-(3-chloro-2-pyridinyl)-1H-pyrazole-5-carboxylic acid N N N O Cl Br OH CAS number: 500011-86-9 Molecular Weight: 302.52 Structural formula: C9H5BrClN 3O2 Observed in: Goat, hen, rat, rice IN-ECD73 CAS name: 2,6-dichloro-4-methyl-11H-pyrido[2,1-b]quinazolin-11-one O N N Cl Cl CAS number: Not available Molecular Weight: 279.13 … Abamectin 1.9 EC 1.00 ml Red Abamectin,ABC,Vertimec 2. The resistance risk is assessed to be low- moderate because of the current pest situation and the intended use of chlorantraniliprole in Norway. 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