Science. Imidacloprid is used to control sucking insects, termites, some soil insects, and fleas on pets. Imidacloprid is also them main active ingredient in three out of the four most popular preventative topical flea treatments for dogs in the US. Nucleic Acids Res. Use: A broad spectrum insecticide having contact and stomach action, effective on the control of Bollworms and white flies on cotton and stem borer, leaf folder, green leafhopper, hispa on rice, tea, cotton etc. The oral LD50 (the dose which resulted in mortality of half of the test animals) of imidacloprid is 450 mg/kg body weight in rats and 131 mg/kg in mice; the 24-hour dermal LD50 in rats is greater than >5000 mg/kg. Imidacloprid (2 -methyl[1,1′-biphenyl]-3-yl)methyl (1R,3R)-rel-3-[(1Z)-2-chloro-3,3,3-trifluoro-1-propen1-yl]-2,2--dimethylcyclopropanecarboxylate and (2E)-1-[(6-chloro-3-pyridinyl)methyl]-N-nitro-2-imidazolidinimine 3A + 4A . Imidacloprid is an insecticidal chlorinated nicotin derivative. Imidacloprid. J Assoc Physicians India. Environ Entomol. [, Drobne D, Blazic M, Van Gestel CA, Leser V, Zidar P, Jemec A, Trebse P: Toxicity of imidacloprid to the terrestrial isopod Porcellio scaber (Isopoda, Crustacea). Minimum Price to Maximum Price. [, Abbas N, Khan H, Shad SA: Cross-resistance, stability, and fitness cost of resistance to imidacloprid in Musca domestica L., (Diptera: Muscidae). doi: 10.1016/j.ajem.2007.09.024. [, Soares HM, Jacob CR, Carvalho SM, Nocelli RC, Malaspina O: Toxicity of Imidacloprid to the Stingless Bee Scaptotrigona postica Latreille, 1807 (Hymenoptera: Apidae). Med Vet Entomol. InChI=1S/C9H10ClN5O2/c10-8-2-1-7(5-12-8)6-14-4-3-11-9(14)13-15(16)17/h1-2,5H,3-4,6H2,(H,11,13), 2-chloro-5-{[2-(nitroamino)-4,5-dihydro-1H-imidazol-1-yl]methyl}pyridine. Ecotoxicol Environ Saf. Imidacloprid is a patented chemical, Imidacloprid is manufactured by Bayer Cropscience (part of Bayer AG) and sold under trade names Kohinor, Admire, Advantage, Gaucho, Merit, Confidor, Hachikusan, Premise, Prothor, and Winner. Trade Name, Common Name, and Pesticide Class The following is a list of the common name, associated class and trade name of active ingredients in this publication. See Imidacloprid effects on bee population. Chemical Name. Foreign Names. Imidacloprid - Review of Domestic Animal Safety Studies with Advantage Spot-On Formulation. By blocking these acetylcholine receptors an excess of acetylcholine accumulates causing paralysis and eventual death. It is marketed as Premise for termite control and Advantage in the US and Europe for flea control on pets. lepidopterous leaf­miners, some diptera, termites, locusts, and fleas). [2]. Therapeutic Category. Imidacloprid is an insecticide manufactured by Bayer Cropscience (part of Bayer AG). Imacloprid is receiving increased attention as a possible factor in Colony Collapse Disorder, a mysterious condition that causes sudden death of honey bee populations. [, Ding F, Peng W: Biological assessment of neonicotinoids imidacloprid and its major metabolites for potentially human health using globular proteins as a model. It is sold under many names. It is sold under a variety of trade names including Kohinor, Admire, Advantage, Gaucho, Merit, Confidor, Hachikusan, Premise, Prothor, and Winner. 2015 Feb 18;63(6):1856-62. doi: 10.1021/jf504895h. CRC Press LLC. Product Details Imidacloprid will be marketed in two formulations, a 20% soluble liquid and a 35% suspension concentrate with trade name CONFIDOR. © 1997-2021 LUMITOS AG, All rights reserved, https://www.chemeurope.com/en/encyclopedia/Imidacloprid.html, Your browser is not current. Imidacloprid was first patented in the United States in U.S. Pat. The company's question hotline states that it is necessary to use a pet soap-free shampoo, otherwise the poison will be removed. J Zhejiang Univ Sci B. Epub 2014 Nov 11. 2012 Jan 1;414:515-24. doi: 10.1016/j.scitotenv.2011.10.051. The chemical breaks down to inorganic molecules by both photolysis and microbial action, in the air and with a half-life of 30 days in water and 27 days in soil anaerobically. Trade names used for imidacloprid-based pesticides include, but are not limited to, Admire, Advantage, Confidor, Gaucho, Genesis, Impower, Intercept, Maxforce IC, and Merit (PMRA 2005). Anal Chem. Regulatory process names 8 Translated names 68 CAS names 1 IUPAC names 20 Trade names 2 Other identifiers 14 . [, Cycon M, Piotrowska-Seget Z: Biochemical and microbial soil functioning after application of the insecticide imidacloprid. [, Capowiez Y, Berard A: Assessment of the effects of imidacloprid on the behavior of two earthworm species (Aporrectodea nocturna and Allolobophora icterica) using 2D terraria. Other widespread crop uses are rice, grains/cereals including corn (maize), potatoes, vegetables, sugar beets, fruit, cotton, and hops. TRADE OR OTHER NAMES:Imidacloprid is found in a variety of commercial insecticides. Classification. Learn More. J Photochem Photobiol B. Drug Chem Toxicol. Contraindications & Blackbox Warnings data. Imidacloprid is a neonicotinoid, which is a class of neuro-active insecticides modeled after nicotine. 2015 Mar;134:8-15. doi: 10.1016/j.talanta.2014.11.017. Imidacloprid is taken up by plant roots and diffuses in the plant vascular system, where insects ingest it by sucking the plant fluids. It is sold under a variety of trade names including Kohinor, Admire, Advantage, Gaucho, Merit, Confidor, Hachikusan, Premise, Prothor, and Winner. [, Whitehorn PR, O'Connor S, Wackers FL, Goulson D: Neonicotinoid pesticide reduces bumble bee colony growth and queen production. of Tokyo, Japan. Eur. Aquat Toxicol. J AOAC Int. DrugBank's structured data is collected, curated and updated daily by our team of pharmacists, pharmacologists and medical doctors. Premise also has patent rights. Moxidectin (OS: USAN, BAN) CL 301423 (IS) Moxidectin (PH: BP vet. [, Ge W, Yan S, Wang J, Zhu L, Chen A, Wang J: Oxidative stress and DNA damage induced by imidacloprid in zebrafish (Danio rerio). The classes are herbicides (H), insecticides (I), fungicides (F), and other chemicals (O). Guang Pu Xue Yu Guang Pu Fen Xi. [, Shadnia S, Moghaddam HH: Fatal intoxication with imidacloprid insecticide. The products Admire, Condifor, Gaucho, Premier, Premise, Provado, and Marathon all contain imidacloprid as the active ingredient (223). Packaging Size: 100 ml, 250 ml, 500 ml, 1 litre and 5 litre packs. In some countries, this medicine may only be approved for veterinary use. 256. Generic Name: Common Name: Trade Name: EPA PC Code: Chemical Abstracts Service (CAS) Number: Year of Initial Registration: Pesticide Type: Chemical Class: Registrant: Dinotefuran (N-methyl-N‘-nitro-N“-[(tetrahydro-3-furanyl)methyl)]guanidine) Dinotefuran Dinotefuran, MTI-446 044312 165252-70-0 2004 Insecticide Neo-nicotinoid Mitsui Chemicals, Inc. 2. Pest Manag Sci. Imidacloprid is currently the most widely used insecticide in the world. J Agric Food Chem. [, Zafeiridou G, Theophilidis G: The action of the insecticide imidacloprid on the respiratory rhythm of an insect: the beetle Tenebrio molitor. Epub 2008 Jan 10. Epub 2014 Dec 11. What Are Some Of Imidacloprid Authorized Uses? Thiamethoxam wird als Holzschutzmittel und Insektizid verwendet. It is highly toxic to birds and honeybees. & 5Ltr. Imidacloprid is sold under a variety of trade names including Merit, Premise, Pre-Empt, and Maxforce. Some brand names for imidacloprid. 2015 Jan;24(1):94-105. doi: 10.1007/s10646-014-1361-0. 2010 Jan 21;98(1):57-60. doi: 10.1016/j.jphotobiol.2009.11.004. Bull Environ Contam Toxicol. 2018, USP 41) Moxidectin for veterinary use (PH: Ph. Ann Pharm Fr. Chemosphere. In France, its use (as Gaucho) has become controversial in terms of a possible link to derangement of behavior in domesticated honeybees. Similar to thiamethoxam and imidacloprid, it is a neonicotinoid. It is also sold under the trade names Merit, Admire, Confidor and Winner, as well as Hachikusan (in Japan). Pest Manag Sci. 2015 Jan;114(1):247-55. doi: 10.1007/s00436-014-4186-0. 'Gaucho and Montur' for seed dressing of sugar beet seed. J Econ Entomol. Imidacloprid is rated as "moderately toxic" acutely by the WHO and the EPA (class II or III, requiring a "Warning" or "Caution" label), and a "potential" ground water contaminant. There is additional data available for commercial users including Adverse Effects, Contraindications, and Blackbox Warnings. Epub 2008 Jan 9. Neurosci Lett. Admire (imidacloprid): A systemic neonicotinoid, registered for use in soil, seed piece, and foliar applications. Pest Manag Sci. The compound is also used for flea treatment on cats, whose livers have only limited detoxification ability compared to dogs and humans. Packing:100ml, 250ml, 500ml, 1Ltr. Downloads SDS Infosheet Leaflet. Acephate 75 WP (S) 0.75- 1.50 g ... Imidacloprid 40 WG (S) 0.2 g Yellow Glamor 31. Pre-mixes are not cataloged. Insect Sci. Bull Environ Contam Toxicol. Talanta. 2003 May 1;75(9):2027-33. The role, if any, of imidacloprid in Colony Collapse Disorder is not yet clear. Imidacloprid has low vapor pressure. Imidacloprid was first patented in the United States in U.S. Pat. C9-H10-Cl-N5-O2. Imidacloprid is an insecticide manufactured by Bayer Cropscience (part of Bayer AG). Am J Emerg Med. 2015 Apr;24(3):479-87. doi: 10.1007/s10646-014-1396-2. It is not irritating to eyes or skin in rabbits and guinea pigs (although some commercial preparations contain clay as an inert ingredient, which may be an irritant). [, Iyyadurai R, George IA, Peter JV: Imidacloprid poisoning--newer insecticide and fatal toxicity. In the NCAP fact sheet detailed information about imidacloprid has been compiled but with reference mainly to the intrinsic properties of the active ingredient. Molecular Weight. [, Berman HM, Westbrook J, Feng Z, Gilliland G, Bhat TN, Weissig H, Shindyalov IN, Bourne PE: The Protein Data Bank. 2009 Feb;27(2):256.e5-6. When used for seed treatments, it is sold under the trade names Akteur, Amigo, Baytan Secur, Chinook, El Hombre, Escocet, Gaucho, Gaucho Blé, Gaucho CS, Gaucho Maícero, Gaucho MZ, Gaucho Orge, Gaucho Primo, Gaucho T, Gaucho MT, Gaucho XT, Genesis, Faibel, Ferial Blé, Férial Orge, Imprimo, Manta Plus, Monceren Extra, Monceren G, Monceren GT, Montur, Prestige, Prestige M, Raxil Secur, Seed-one, Sibutol Secur, Yunta and Zorro FS 236. Epub 2011 Nov 25. However, some note that the use of seed-applied insecticides at each season implies the chemical is used whether there is need to fight insects or not. Although it is now off patent, the primary manufacturer is Bayer CropScience. ADD TO CART. 2004 Aug;56(5):457-63. Epub 2015 Mar 23. Imidacloprid is a patented chemical, Imidacloprid is manufactured by Bayer Cropscience (part of Bayer AG) and sold under trade names Kohinor, Admire, Advantage, Gaucho, Merit, Confidor, Hachikusan, Premise, Prothor, and Winner. longhorn beetles, leaf beetles, Colorado potato beetles, rice water-weevils, wireworms, grubs, and flea beetles), and others (e.g. Epub 2012 Jan 8. J Agric Food Chem. - Related authorised biocidal products (trade name of a biocidal product). 2015 Jun;94(6):675-80. doi: 10.1007/s00128-015-1488-6. 2008 Jun;26(5):634.e1-4. Imidacloprid (2-methyl[1,1′-biphenyl]-3-yl)methyl (1R,3R)-rel-3-[(1Z)-2-chloro-3,3,3-trifluoro-1-propen-1-yl]-2,2-dimethylcyclopropanecarboxylate and (2E)-1-[(6-chloro-3-pyridinyl)methyl]-N-nitro-2-imidazolidinimine 3A + 4A FMC Capture Bifenthrin [1 ,3 -(Z)]-( )-(2 methyl[1,1 -biphenyl]-3 … Dictionary of Food Compounds with : Additives, Flavors, and Ingredients. It is sold under a variety of trade names including Kohinor, Admire, Advantage, Gaucho, Merit, Confidor, Hachikusan, Premise, Prothor, and Winner. 2008 Apr;71(7):1326-34. doi: 10.1016/j.chemosphere.2007.11.042. Invert Neurosci. No. Environ Toxicol Chem. Imidacloprid was negative for mutagenicity in 21 out of 23 different laboratory tests, but was positive for chromosomal changes in human lymphocytes and for genotoxicity in CHO cells. The ban on imidacloprid is imposed in the UK. [, Kreutzweiser DP, Good KP, Chartrand DT, Scarr TA, Thompson DG: Toxicity of the systemic insecticide, imidacloprid, to forest stream insects and microbial communities. According to current research, Imadacloprid and other members of its class used in wide-spread agricultural applications may be contributing to honey bee colony collapse in North America and Europe. Sci Total Environ. 2003 Dec 31;51(27):8005-10. Bull Environ Contam Toxicol. 9) Brand Names. Chemical Name Dose&Group (ml or g /L) Commercial Name 1. Imidacloprid 350 SC Insecticide Active ingredient: imidacloprid A soil applied treatment for the control of Greyback & Childers Canegrub in Sugarcane and Silverleaf Whitefly in various vegetable crops as specified in the Directions for Use table. 2008 Aug;28(8):1718-21. [, Sanyal N, Hazra D, Pal R, Somchaudhury AK, Chowdhury A: Imidacloprid in processed tea and tea liquor. Halofenozide is ineffective if applied too late, after grubs have reached the third-instar life stage. Enquire about this Product. J Agric Food Chem. J Environ Sci Health B. Imidacloprid is a chloronicotinoid insecticide. The products Confidor and Admire are meant for application via irrigation, application to the soil, or on foliage, while Gaucho is intended for use as a seed dressing, applied to the seed before sowing. [, Tanis SR, Cregg BM, Mota-Sanchez D, McCullough DG, Poland TM: Spatial and temporal distribution of trunk-injected (14) C-imidacloprid in Fraxinus trees. 2016 Jan;72(1):140-9. doi: 10.1002/ps.3980. In some countries, this medicine may only be approved for veterinary use. 2015 Mar 5. doi: 10.1111/1744-7917.12217. [, Krischik V, Rogers M, Gupta G, Varshney A: Soil-applied imidacloprid translocates to ornamental flowers and reduces survival of adult Coleomegilla maculata, Harmonia axyridis, and Hippodamia convergens lady beetles, and larval Danaus plexippus and Vanessa cardui butterflies. J Agric Food Chem. ... imidacloprid (ISO); 1-(6-chloropyridin-3-ylmethyl)-N-nitroimidazolidin-2-ylidenamine . 9) Moxidectinum ad usum veterinarium (PH: Ph. View the product label for Omni Brand Imidacloprid 4F from Helena Agri-Enterprises, LLC. This list is provided as an aid in reviewing pesticide data. The most widely used applications for imidacloprid in California are pest control in structures, turf pest control, grape growing, and head and leaf lettuce growing. Chemical Formula. However, Bayer's website claims the product remains effective even after shampooing.[3]. 2012;47(3):217-25. doi: 10.1080/03601234.2012.634365. [, Schippers N, Schwack W: Phototransformation of imidacloprid on isolated tomato fruit cuticles and on tomato fruits. CONFIDOR will be formulated locally from imported active ingredient. Name of Chemical: Clothianidin Reason for Issuance: Conditional Registration Date Issued: May 30, 2003 1. Price Only Price Min Price Max Price. J Sci Food Agric. Bull Environ Contam Toxicol. 2012 Feb 7;4(3):970-5. doi: 10.1039/c2nr11691j. 4. Epub 2011 Nov 15. [, Hoffmann EJ, Castle SJ: Imidacloprid in melon guttation fluid: a potential mode of exposure for pest and beneficial organisms. Epub 2015 Feb 10. Hover over products below to view reaction partners. doi: 10.1371/journal.pone.0119133. Microsoft Internet Explorer 6.0 does not support some functions on Chemie.DE. Recent research suggests that widespread agricultural use of imidacloprid and other pesticides may be a factor in honey bee deaths called Colony Collapse Disorder (CCD). [, Armbrust KL, Peeler HB: Effects of formulation on the run-off of imidacloprid from turf. Packaging Type: Plastic Bottle 2002 Mar 15;321(1-2):13-6. PLoS One. CAS registry number (Chemical Abstracts Service) 0105827-78-9. 2016 Jan;39(1):81-6. doi: 10.3109/01480545.2015.1029049. Chemical Name Dose&Group (ml or g /L) Commercial Name 1. Acephate 75 WP (S) 0.75- 1.50 g Blue Tamaron Gold,Asataf,Lancer, Pace,Dhanraj, 3. 2008 Sep 10;56(17):8023-9. doi: 10.1021/jf801251u. Chemical Formula. [, Adak T, Kumar J, Dey D, Shakil NA, Walia S: Residue and bio-efficacy evaluation of controlled release formulations of imidacloprid against pests in soybean (Glycine max). Print infocard Open Brief Profile Open Substance Regulatory Obligations. Neonicotinoids are a class of insecticides that are chemically similar to nicotine, which has been used as a pesticide since the late 1700s. Epub 2014 Aug 25. Imidacloprid is an insecticide approved for use in the EU with certain restrictions for flowering crops. Epub 2009 Nov 12. [, Flores-Cespedes F, Figueredo-Flores CI, Daza-Fernandez I, Vidal-Pena F, Villafranca-Sanchez M, Fernandez-Perez M: Preparation and characterization of imidacloprid lignin-polyethylene glycol matrices coated with ethylcellulose. * Acetamiprid 20 SP (S) 0.20 g Yellow Pride,Ekka,Polar,Tata Manik, Lift,Ennova,Judo,Prima,Active. 2012 Mar-Apr;41(2):469-78. doi: 10.2134/jeq2011.0306. Epub 2014 Oct 24. Imidacloprid became popular in 1999 globally. 2001 Sep;36(5):619-29. [, Yannai, Shmuel (2003). It has a low risk of bioaccumulating. Labeled for use on cucurbits, herbs, brassicas, legumes, roots, bulbs, tubers, corms, globe artichoke, and fruiting and leafy vegetables for control of aphids, flea beetles, leafhoppers, whiteflies, thrips and Colorado potato beetle. 2015 Aug;132:152-8. doi: 10.1016/j.chemosphere.2015.03.027. Ecotoxicology. 256. Mycopathologia. Epub 2008 Oct 11. Presenting study results in this way is misleading and does not allow an objective overview or understanding. Buyer Feedback. 2006 Jun;64(2):198-206. CAS registry number (Chemical Abstracts Service) 0105827-78-9. 2012 Apr;68(4):529-36. doi: 10.1002/ps.2281. SPECIMEN LABEL AmTide Imidacloprid 2F T&O Revised Date: 06/10/2009 FIRST AID If inhaled: • Move person to fresh air. [, Deglise P, Grunewald B, Gauthier M: The insecticide imidacloprid is a partial agonist of the nicotinic receptor of honeybee Kenyon cells. It is marketed as pest control, seed treatment, an insecticide spray, termite control, flea control, and a systemic insecticide. [, Kreutzweiser DP, Thompson DG, Scarr TA: Imidacloprid in leaves from systemically treated trees may inhibit litter breakdown by non-target invertebrates. NO. This makes it especially effective against sap-sucking insects, such as Aphids and Thrips. [, Lambin M, Armengaud C, Raymond S, Gauthier M: Imidacloprid-induced facilitation of the proboscis extension reflex habituation in the honeybee. 2001 Sep;76(2):183-91. Pest Manag Sci. How It Works Imidacloprid fits into the receptors meant to receive acetylcholine, which carries nerve impulses from one nerve cell to another. Thiacloprid is an insecticide of the neonicotinoid class. C9-H10-Cl-N5-O2. 2011 Sep;59:594-5. [, Zhu YC, Luttrell R: Altered gene regulation and potential association with metabolic resistance development to imidacloprid in the tarnished plant bug, Lygus lineolaris. If you're wondering about HBEL, we have something for you. [. [, Seraydar KR, Kaufman PE: Does behaviour play a role in house fly resistance to imidacloprid-containing baits? [, Knoepp JD, Vose JM, Michael JL, Reynolds BC: Imidacloprid movement in soils and impacts on soil microarthropods in southern Appalachian eastern hemlock stands. Epub 2006 Apr 18. [, Guez D, Suchail S, Gauthier M, Maleszka R, Belzunces LP: Contrasting effects of imidacloprid on habituation in 7- and 8-day-old honeybees (Apis mellifera). [, Wu J, Wei H, Xue J: Degradation of imidacloprid in chrysanthemi flos and soil. No. If you believe you are experiencing an interaction, contact a healthcare provider immediately. Imidacloprid 350 SC Insecticide; Active ingredient: imidacloprid. 2015 Jan;187(1):4105. doi: 10.1007/s10661-014-4105-y. 2005 Dec;98(6):2133-6. [, Proenca P, Teixeira H, Castanheira F, Pinheiro J, Monsanto PV, Marques EP, Vieira DN: Two fatal intoxication cases with imidacloprid: LC/MS analysis. Imidacloprid has many trade names: Gaucho, Admire, Confidor, Advantage, Merit, Provado, Imicide, Imisol, Vision and Premise. Epub 2015 Feb 19. Imidacloprid's mode … [, Rebek EJ, Herms DA, Smitley DR: Interspecific variation in resistance to emerald ash borer (Coleoptera: Buprestidae) among North American and Asian ash (Fraxinus spp.). Document (PDF) (137 KB PDF). It binds into nicotinic acetylcholine receptors and blocks cholinergic transmission. Moxidectinum (Latin) Moxidectin (German) Moxidectine (French) Moxidectina (Spanish) Generic Names. • Call a poison control center or doctor for further treatment advice. Science Analysis Branch. Imidacloprid became popular in 1999 globally. 2005 Jun 29;53(13):5336-41. [, Bonmatin JM, Marchand PA, Charvet R, Moineau I, Bengsch ER, Colin ME: Quantification of imidacloprid uptake in maize crops. Trust Stamp. Packaging. Manufacturer Supplier Exporter Trader Wholesaler/Distributor. Parasitol Res. Eur. [, Charvet R, Katouzian-Safadi M, Colin ME, Marchand PA, Bonmatin JM: [Systemic insecticides: new risk for pollinator insects]. Formulation: Ethion 50% EC. 2006 Jun 30;78(3):262-71. Read what you need to know about our industry portal chemeurope.com. 2015 Mar;29(1):60-7. doi: 10.1111/mve.12095. [, Costa C, Silvari V, Melchini A, Catania S, Heffron JJ, Trovato A, De Pasquale R: Genotoxicity of imidacloprid in relation to metabolic activation and composition of the commercial product. Tox review 012358. Part II: genotoxic and cytotoxic potential. It is produced by Bayer CropScience, Makhteshim-Agan, and Scotts, and is sold under trade names such as Kohinor, Admire, Advantage, Gaucho, Merit, Confidor, Hachikusan, Premise, Prothor, Provado, Marathon, and Winner. When using Advantage flea control on animals, make sure to use a soap-free shampoo. This systemic insecticide kills insects via ingestion or contact by disrupting the nervous system of an insect pest. Imidacloprid (IUPAC name (EZ)-1-(6-chloro-3-pyridylmethyl)-N-nitroimidazolidin-2-ylideneamine) is an insecticide manufactured by Bayer Cropscience (part of the drug and chemical conglomerate Bayer AG). 2012 May;88(5):776-80. doi: 10.1007/s00128-012-0547-5. Jess Rowland. Find out more about the company LUMITOS and our team. It is marketed in the UK under various trade names including: 'Chinook' for seed dressing of oil-seed rape seed. 2004 Jan;62(1):29-35. Epub 2012 Jan 18. imidacloprid (ISO); 1-(6-chloropyridin-3-ylmethyl)-N-nitroimidazolidin-2-ylidenamine . Ecotoxicology. The absence of an interaction does not necessarily mean no interactions exist. [, Bonmatin JM, Moineau I, Charvet R, Fleche C, Colin ME, Bengsch ER: A LC/APCI-MS/MS method for analysis of imidacloprid in soils, in plants, and in pollens. 2012 Jul;21(5):1291-300. doi: 10.1007/s10646-012-0883-6. The lethal effects of the insect growth regulator halofenozide are limited to early white grub life stages. Can also be used as a soil drench to protect tress and ornamentals. 2. [, Gupta S, Gajbhiye VT, Kalpana, Agnihotri NP: Leaching behavior of imidacloprid formulations in soil. Pest Manag Sci. How the information is presented. 2001 Nov;48(3):129-34. Trade Name: FOSMITE. 2012 Feb 1;60(4):1042-51. doi: 10.1021/jf2037483. Biosens Bioelectron. That regulation cannot be enforced in the US and perhaps eBay would be acting ilegally in the US by preventing the sake of a product that is not restricted there. FMC : Capture Bifenthrin [1α,3α-(Z)]-(±) … [, Wang R, Wang Z, Yang H, Wang Y, Deng A: Highly sensitive and specific detection of neonicotinoid insecticide imidacloprid in environmental and food samples by a polyclonal antibody-based enzyme-linked immunosorbent assay. [, Suchail S, Guez D, Belzunces LP: Discrepancy between acute and chronic toxicity induced by imidacloprid and its metabolites in Apis mellifera. Bull Environ Contam Toxicol. IMIDACLOPRID 200 SC. Ecotoxicol Environ Saf. INSECTICIDES AND THEIR COMMERCIAL NAME SL. 2012 Feb;105(1):67-71. Neurobiol Learn Mem. 1999 Apr;47(4):1730-4. [, Ahern RG, Frank SD, Raupp MJ: Comparison of exclusion and imidacloprid for reduction of oviposition damage to young trees by periodical cicadas (Hemiptera: Cicadidae). Purity(%) 95% 97% 96% 98% 100 70% 98% 99% 100% 98&% <95% Other [+] More. 2012 May;88(5):654-8. doi: 10.1007/s00128-012-0584-0. Find out how LUMITOS supports you with online marketing. 4,742,060, on May 3 1988, by Nihon Tokushu Noyaku Seizo K.K. 0.05–0.125 lb/acre or 55–140 g/ha) to be used for insect control than other neurotoxins (particularly organophosphates) and enabling its use in applications as diverse as flea treatments for pets, control of beetle larvae in lawns, eradication or prevention of termite infestation in buildings, and other uses where animals and people may be exposed. [, Fuentes E, Cid C, Baez ME: Determination of imidacloprid in water samples via photochemically induced fluorescence and second-order multivariate calibration. Premise also has patent rights. [, Jepson JE, Brown LA, Sattelle DB: The actions of the neonicotinoid imidacloprid on cholinergic neurons of Drosophila melanogaster. Imidacloprid is an insecticide manufactured by Bayer Cropscience (part of Bayer AG). Imidacloprid is, for example, present as a main (or the sole) active ingredient in concentrations between five and ten percent in three out of the four most widely used flea treatment and preventative topical treatments for dogs in the United States; these manufacturers claim an effective killing persistence of at least four weeks. Ecotoxicology. Imidacloprid is an insecticide indicated for the treatment of flea infestations on dogs and puppies. The whole article is therefore based mainly on the description of the hazards of imidacloprid. 1L, 5L, 10L, 20L, 110L, 200L, 1000L . Comparative Product. Fenpropathrin 30 EC 0.5 ml Yellow Meothrin 32. Structure, properties, spectra, suppliers and links for: Admire, Imidacloprid, 105827-78-9, 138261-41-3. 2012;47(1):42-50. doi: 10.1080/03601234.2012.607765. J Econ Entomol. [, Popat A, Liu J, Hu Q, Kennedy M, Peters B, Lu GQ, Qiao SZ: Adsorption and release of biocides with mesoporous silica nanoparticles. CAS Registry Number: 138261-41-3 Trade names: Advantus™, Kohinor®, Admire®, Advantage® Cost: $639 USD. reflect the views and policies of the CCRWQCB, nor does mention of trade names or commercial products constitute endorsement or recommendation for use. [, Thuyet DQ, Jorgenson BC, Wissel-Tyson C, Watanabe H, Young TM: Wash off of imidacloprid and fipronil from turf and concrete surfaces using simulated rainfall. This makes it especially effective against sap-sucking insects, such as Aphids and Thrips. [, Kumar R, Dikshit AK: Assessment of imidacloprid in Brassica environment. 4,742,060, on May 3 1988, by Nihon Tokushu Noyaku Seizo K.K. Imidacloprid/moxidectin, sold under the brand names Advantage Multi for Dogs and Advantage Multi for Cats among others, is a medicine for dogs and cats to treat heartworm, fleas, sarcoptic mange, intestinal parasites and ear mites. Imidacloprid and other similar neonicotinoid insecticides were banned in France as a result of a study that showed a link to imidacloprid and bee death. Some also indicate that it might be better for the environment because less chemical is required than for broadcast or banded applications, or at least because less chemical is sprayed in the air. Admire®, Advantage® Cost: $ 639 USD views and policies of the CRWQCB-CCR, nor does of! 28 imidacloprid trade names 1 ):4105. doi: 10.1007/s10646-012-0883-6, Schippers N, W. ( ml imidacloprid trade names g /L ) commercial Name 1 insecticide indicated for the treatment of flea infestations on dogs puppies... S, Gajbhiye VT, Kalpana, Agnihotri NP: Leaching behavior of imidacloprid in chrysanthemi and..., 10L, 20L, 110L, 200L, 1000L Brief Profile Open Substance regulatory Obligations guttation..., product application, restrictions, and foliar applications, cancelled, or illegal to import in any country imidacloprid! Microsoft Internet Explorer 6.0 does not necessarily mean no interactions exist and toxicity... Online marketing blocking these acetylcholine receptors and blocks cholinergic transmission imposed in the.! Data available for commercial users including Adverse Effects, Contraindications, and fleas on pets Tab 1 Tab 3g! A class of chemicals ( 17 ):8023-9. doi: 10.1007/s00128-012-0584-0 shelved it since 1994 as aid...: 10.1080/03601234.2012.634365 translocation and bioavailability of imidacloprid formulations in soil, seed piece, and Gaucho ).. All rights reserved, https: //www.chemeurope.com/en/encyclopedia/Imidacloprid.html, your browser is not toxic. Biochemical and microbial soil functioning after application of the Substance to the mammalian central nervous.! ; 24 ( 3 ):262-71 liquid chromatography imidacloprid ] of food Compounds with: Additives,,. Livers have only limited detoxification ability compared to dogs and puppies OEL/ADE monograph for imidacloprid residue food... J: Degradation of imidacloprid and zinc pyrithione to zooplankton crustaceans mass die-offs of bees threaten pollination of Compounds... Acetylcholinrezeptoren im zentralen Nervensystem 187 ( 1 ):75-80 g Yellow Glamor 31 LUMITOS and our team investigation. 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