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Title 農薬の名称 Author(S) 大野, 稔 Citation 防虫科学 (1956), 21(2

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Title 農薬の名称 Author(s) 大野, 稔 Citation 防虫科学 (1956), 21(2): 54-62 Issue Date 1956-05-29 URL http://hdl.handle.net/2433/156936 Right Type Departmental Bulletin Paper Textversion publisher Kyoto University 防 虫 科 学 郡 21 巻-T 雑 録 CommonNaJneSOEPesticidesMino印 OfI y0 ,BoLyu-Kagahu21 , 弘,1956. 13 ･､農 薬 の 名 称 . 大 野 稔 近咋多種多様の良薬の出葺削こより,ややもするとその名称に混乱を来 しそうである｡ 米国では T. Econ.Ent. , に用ひる殺虫剤の名称は ⅠnterdepartmentalCommitteeofPestControl で公認 された commonname のあるものは･ その名称 を 用ひなlすればな らないこととされて JF_tる｡ 其の他に, 独 占的でよく知 られた田有名や会社番号名の ものは 大文字をつけて用ひて も よい｡ 又長い間親 しまれた名称で改名すると混乱する恐れのあるものや, 分子中の原子,原子 団の位置を省略 した短い化学名な どは, そのまま使用 して もよいこととされて居 る｡ 次 に共等 の朝出剤及び教程の殺菌剤の名称 (下表 ･左仙)を示す｡ ComⅡ10JINamesoflnSeCticides NA hLJ.i HT,o BR D EFIyI,mi ･TO.TiITEでIA諾 SDr言霊NATl冨T3Ds .lldrin notlessthan95percentof1 ,2, 3,4,10,10- compourid118 hexachloro l1, 4,4a ,5,8,8a-hexahydr0-1 ,4,5,. 8-dimethanonapbtbalene .lllcthrin dE-2 lally1-41hydroxy-3-methy1-2-cyclopenten- allyll10mOlogofcinerin1 1-oneesterifiedwithamixtureofGisand syntheticpyrethrins ･ tramsdZ-Chrysanthemummonocarboxylicacids ^m.Cy.lnamid 3911 0,0-diethylS-ethylmercaptomethyldithio - pl10Sphate ^m.Cy.lnamid4124 0 -(2-cわlor(I-4-mitropheny l)-0,0 -dimethyl isochlorthion t】liophosphate ^rn.Cyanamid12008 0 ,0-diethyl.S-isopropylmercaptO-methyl dithoplloSphate ^m.Cyammid1200rJ 0,0-diethyl.Sl1Z-PrOpylmercapto一methyl dithiophospbate Am.Cy.lnamid12013 0,0 -diisopropylS-isopropylmercapt0-methyl dithiophosphate ^r.lmite productcontaining2-(p-tert-I)utylphenoxy) compoundSSR isopropy1-1-methylethy 1 2-chloroethyl-sulfitealkylarylsulfite azobenzene azobenzide - diphenyldiimide Baycr21/199 3-clllor0-4-metbylumbelliferone-0,0-dietllyl tbiop土10Spllate Payer21/200 3-chlor0-41methylumbelliferone-0 ,0-dimethyl thiophosphate BayerL 13/ 59 0,0 -dimethy12 ,2,21trichlorol1-hydroxy- ethylphospl10nate Bayer28/63 〔2-(diethoxyphospllinylthiq)ethyl〕ethy1-methyl sulfoniummethylsulfate / Payer16259 0 ,0-diethyl-S-(4-oxo-benzotriazinol3-methyl) ahenzotria2:inederivativeof pbospllOrOdithioate anethylditlliopllOSpllate payer17147 0,0 -dimethyl-S-(4-oxo-benzotriazin0-3-me- abeIIZOtriazinederivativeof tbyl)phospborodi tb ioate amethyldithiophosp h ate 11ⅠIC 1,2,3,4,5, 6-hexachlorocyclohe羊ane,Consisting benzenehexachloride,666 ofseveralisomersandcontaining12to1 4 gammeXane･ percentofthegammaisomer 64 UJ' 山 村 学 郡 21 ･yu8-T OTEJm D ESTON^TrONS N^ 刈ETO nlC Df!FTFrTTTON tlZIRD TrT^T lⅠ^vT:n 7叩:Nt ISEn Buhn 1.1-his (p -chlorophenyl) -2lnZtrobutane CS-674A butoxypolypropylene CragFュyRepellent glyCol hlltOXythiocyanodiethyl 2-1JlltOXy-2'-thiocyanodiethylether Letbane384 ether CIllorr)benzihte ethy14,4'-dlchlorobenzilate Geig y331q G-23992 chlordane 1,2 ,14 ,r) .6,7,8,8-Octachlor0 -2,313a ,4,7,7a - chlordan hexahydr0-4 ,7-methanoindene Velsicol1068 0cta-Klor octichl.r Chlorthion 0 -(3-chloro-4-nitrophenyl) -0,0 -dimethyl rhyer22/In° thiopI10Sphate eyclethrin dl121(2 -cyclopentynyl)-4-hydroxy-3-methy1-2- cyclopenten l1-oneesterifiedwithamiⅩture ofGisandtrans dZ-chrysanthemummonomr- boXylicacids D-Dmixture mixtureof1 ,2-dichloropropaneand1 ,3- D-D dicbloropropene. D oly∫umeN I)DT Commerciallyavailabledichloro-djphenyl- chlorophenoth:lne trichloroethane,theprincipalconstitllent (U.S.PharmarOPOelh ofwhichis1 ,1,11trichlor0-2 ,2-biS(i)-chlo ･ 14:1:36.lni'JO) rophenyl)ethane ?,tI-T)r)T 1,1,1-trichlor0-2 ,2-his(p-chlorophenyl)ethnc nDVll dimethy12 ,2-dichlorovinylphosphate llerntLtOn mixtureof0 , 0-diethyl-S-ethylmereaptoethyl .1tri.llkylthiophosJ)h.lIe thiophosphateand0 ,0 -diethyト0-ethylmcr- mptoethylthiophosphate Dhzinrm 0,0-diethyl O 一(21isopropy1-6-methyl 14-pyri - G･244糾 midinyl)thiopb0Spbate dichloroethylether bet .1 ,7)eta'-dichloroethylether 1-ehloro-2(bcta - chloroethoxy)eth.lnC dichlorophenylbenzene- 2.4-dichlorophenylhenzenesulfonatc Gellite sulfonate Geni上()1923 dieldrin notlessthan85percentof1 ,2.3,4,10,101 compollnd497 bexacblor0-6 , 7-epoxy-1 ,4,4a-5 ,6,7,8,8a- octahydr0-1 ,4,5,8-dimethanonaplltbalene diisopropylparathion 0,0 -diisopropyl0-♪･nitropbenylthiopl10S- compound34lJ6 phate T)jhn mixtureof1partofProlanand2partsof CS-708 Jlulan dimefox his(dimcthylamino)8uorophosphineoxide IIanane dimethylcarbate dirnethylGis-bicyclol2.2.1) -5-heptene-2 ,31 dicarboXylate･ dinitroblltyl-phenol 4,6-dinitr0-0-5eC-butylpllenO1 Dinoseb DNOSBP dinitrocycloheXylpllenOl 4,6-dJ'nitr 0 -0 ICydohexylpheno1 DNOCHP' Dinex dinitrocresol 4,0-din]'t ro IO-ere.q()I DNOC DNC Sidox 65 防 虫 科 学 郡 21 . 巻 一甘 N^ユ柑TOI17T DI;FINlTLOh' OTIIJTRDF:SrGNATIOh,S tIST･:D TTr^TZrAV r; ll TYTl:NVsF;D dithiocyanodiethylether beta,beta′-dithiocyanodiethylether Lethane A -70 I)MC 4,4′-dichloro-alpha-methy l henzhydro1 di(クーcbloropbenyl) methylcarllinol 1,1-his(♪-chlorophepyl) ethanol,Dimite DolyF .T-14 0,0 -dimethyl02 ,4,5-trichlorophenyl phospl10rOthioate DowET･1lJ 0-methy 10 -2,4,Tトーrichlorophenylphosphor- amidotbioate cndrin 1,2,3,4･10,10-hexachloro -G,7-epoxy ･1,4,4a ,5, Compound2-m 6,7,8,8a10Ctahyd r 0-1,4,r) ,8-endo-endo - dimethanonaphthalene 0-ethylO-かnitrophenylhenzenethiophospho- F.PN_300 ' EPN mate ethylhex-Tlnerliol 2-ethyl-1 I3-hexanediol ＼ lく1】tgerS612 fllrethrin dZ-2-(21furfuryl) -4-hydroxy-3-methシ1 12- I ､ cyclopenten- 1 -Oneesterifiedwith'amiⅩture ofGisandtransdL-chrysanthemummono- carboXylicacids hcpt.TIChlor 1(or3 a).4 ,5,6,7,8,8-heptachlorol3a ,4,7,7a-velsic｡1104 tetraIlydr0-4 ,7-metllanOindane E-3314 ･ H F.'rP mixtureofethylpolyphosphatescontaining hexaethyltetraphosph.TttC 12t｡20percentoftetraethylpyrophosphate ITolcornhcompound32G 0,0 -diisopropyldithiophosphoricacidester of N,N-diethyldithioca ri 'amicよnhydrosulfide Ind.llone l笠 n31 64二:tih.:odxr;'1-a2:e21dimethyl ~410 X O~2 1ト 'Z-1':Yaltemesityloxitlc butopyronoxy1 is()TJOrnylthl'dcyano- terpinylthiocyanoaぐChtC acct.ltC Tbanite is lにhlorthitm 0 -(2-chlor0-41nitrophenyl)-0,0-dimethyl compound4124･ thit)phosphate isodrin l･2･3,4,10,101hexachlor0-1 ,4,4a ,5,8,Ba-hexa - Icompound711 hydr0-1 ,4,5,8,-endo-end()-dimethanonapb- thalene G-23611 Isohn dicmaertlTayLa6:e(1-isopropyl~3~mcthylpyrazolyu lLaralhanc dinitro(1-methylheptyl)PhenylerotQnate lauscttInell ChloromethylL)-chlorophenylsulfone lin(hnc gammaisomerof13HC ofnotlessthan 99 gammaliIiC percentpurity malathon -alathion Old?I-hdil怒atohsyplh-aSt- e(1 ･2-dicarboxyethyl) compound40 19 Metacide productcontaining m ethylparathionand parathion methoxychlor 1,1,1-trichloro 12･2-I)is(p-rncthoxypheny) - Marlate ethane 1) lWD T -ethylde-eton mli諾uyrleaOnfd Oo',0 .I_ddiimmeetthhyyi-_S.-_eeThyyllmmeer ,ccaaPptt Oo-_ ethylthiophosphates methylparathion O' O-dimethyl0-p-nitrophenylthiophosphate methylhomo10gof parathion MGK2 64 N-(2-ethylhexyl)bicyclo 〔2,2,1〕 151heptene- loctacl'de261 2,3-dicarboximide VanDyk264 mipafox ∴ his(isopropylamino)Lluorophosphineoxide .甲 yJ 虫 料 や 那 21 だ.BIT N^Lは･110 rlT.: I)F.FL h' rT10N OTm･: R D EB.TOy^TIOyS tJS7TD TEIAT lrAVR BT･:EN tIFlF:T) -Neotmn productcontain lnghis (p -Chlorophenoxy) - di(47cIlloropIlenOXy) mcthane methane K-1875 Npn tetrapropyldithiopyrophosphate OVeX かchlorophenylかchlorobenzenesulfonate 0votranK-6451 Ovl)tram productcムntainjngp-ぐhloropheTyl♪-ch16ro- 冗 -64.51 henzenesulf(】nate Par;トOXOn oxygenanalogofpaT'a- die thyl♪ i troph en ylph osp hate thion E-600 p.lrathion 0,0-diethyl 0-1･-nitrophenylthiophosphate E-605 compound3422 Perth:lTle 1,1-dichloro 12,217)is (♪-ethylphenyl)ethILne Q1137 pIPerOny17)tJtOXide productcont.liningasitsprlnCipalconstituent. (butylcarbitol) Lllpha- 〔2-(2-hutoxyethoxy)-ethox y 〕-4,6- (6-propylpiperonyl) methylenedioxy -2-propyltoluene ether comopund312 piperonyl cyclonene mixtureof3-alkyト6-carbethoxy-5(3 ,4･ pIPerOnyl cy clohexenPne methylenedioxyphenyl) -2- cy clohexenel 1 - oneand3-a】kyll5(3 ,4-methylenedioxyphcnyl) 2- cy clohexene-1-one Pirazinrln 0,0-diethy13 1(2-propy1 -6-methy1-41Pyr王mi- G･24622 dinyl)thiopDosp h atと Pot.iSan 4-methyluml)ellifer(1ne 0 ,0-dietllyl E-838 thioph｡sphate 0,0-diethylthio- phosphoricacid esterof7-bydroxy- 4-methylcoumarin PTOhn 1,1-7)is(Z･-chlorophenyl) -2-nitroprop.lne cS- 645A prr)pylisnme di-n-propy1 -21methy1-6 ,7- n?ethylenc(1ioxy l1, 〟-propylisome 2,3,4-tetrahydronapbthalene-3 ,4-dicarhqX- ylate Pymzoxon 0 ,0-diethyl0 -5-( 3-methylpyrazolyl)phosphate G-24483 ･Pyrolan dimethy15 -(3-methyト1-pbenylpyrazoly り- G-22008 Carbamate Rohm皮 ‖aasFW -152 1,1-his(p -Chlorophenyl)2 ,2-dichloroethanol Rohm皮 ‖aasFW ･293 1,1-his(p -Chlorophenyl )2,2,2-trichloroethanol schradan octamethylpyrophosphoramidc his(his-(lirhethylamino) pl叩SPhonousanhydride Pestox:III OMPA £es:tmln 2,6-his(3 ,4-methylenedioxyphenyl)-3 ,7- dioxahi cy clo〔3:3･0〕octazle sesamoljn L'-(3,4-methylenedioxy'phenyl)-6-(3 ,4-I methylenedioxyphenoxy) 13,7･dioxabi cy clo･ 〔3.3.0〕octane sllellOS1836 diethy12-ehlorovinylphosphate shellOS2046 1-C.lrIJprnethoxy-1-propen-2-yldimethyl′ ph()sphate Strobane .lterPenCPOlyCh70rimtelyitha/Chlorine compound3961 contentofnpproximnte)y6Opercent- sulfotepp 0,0 .0,0 -tctr;tethyl･dithiopyrlopho-qphate ditbione Sulfatep Lr JT rJJ'L山ノ科 学 弟 21 巻-T OTHER DIはIQNATIO加S N^N TSTO DJI D IでFINITION tISTl.' D TIIATZIAVR BEJTNtlsl弓D sulLoxide n-octyliulfoxideofisosafrole Sulfox-Cide SulpIlenOne productcontainingpIChlorophenylphenyl R-242 sulfoneandrelatedsulfones Systo又 productcombiningdemeton TDE commercia.llyavailabledichloro-dipheny1- ODD dichloroethane,theprlnCipaleomstituent- Rhothane oEwhichis1 ,1-dichloro 12,2-his tetrachlorodiphenyl - (カーcbloropbenyl)etbane etbane TEPP tetraethylpyrophosphate TEP thiocyanoethyllaurate beta-thiocyanoethyllaurate Letbane60 toxaphene chlorinatedcapphenehavingachlorine compound3956 contentof67-69percent. ･CommonNAme80fFtugicideJ9 OTHER D】ミSIGNATIONb N ^ N7;TOBTCtJSmD
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    The WHO Recommended Classi cation of Pesticides by Hazard and Guidelines to Classi cation 2019 cation Hazard of Pesticides by and Guidelines to Classi The WHO Recommended Classi The WHO Recommended Classi cation of Pesticides by Hazard and Guidelines to Classi cation 2019 The WHO Recommended Classification of Pesticides by Hazard and Guidelines to Classification 2019 TheInternational Programme on Chemical Safety (IPCS) was established in 1980. The overall objectives of the IPCS are to establish the scientific basis for assessment of the risk to human health and the environment from exposure to chemicals, through international peer review processes, as a prerequisite for the promotion of chemical safety, and to provide technical assistance in strengthening national capacities for the sound management of chemicals. This publication was developed in the IOMC context. The contents do not necessarily reflect the views or stated policies of individual IOMC Participating Organizations. The Inter-Organization Programme for the Sound Management of Chemicals (IOMC) was established in 1995 following recommendations made by the 1992 UN Conference on Environment and Development to strengthen cooperation and increase international coordination in the field of chemical safety. The Participating Organizations are: FAO, ILO, UNDP, UNEP, UNIDO, UNITAR, WHO, World Bank and OECD. The purpose of the IOMC is to promote coordination of the policies and activities pursued by the Participating Organizations, jointly or separately, to achieve the sound management of chemicals in relation to human health and the environment. WHO recommended classification of pesticides by hazard and guidelines to classification, 2019 edition ISBN 978-92-4-000566-2 (electronic version) ISBN 978-92-4-000567-9 (print version) ISSN 1684-1042 © World Health Organization 2020 Some rights reserved.
  • Opis Patentowy 130618 Rzeczpospolita Lodowa

    Opis Patentowy 130618 Rzeczpospolita Lodowa

    POLSKA OPIS PATENTOWY 130618 RZECZPOSPOLITA LODOWA Patent dodatkowy do patentu nr — Zgłoszono: 82 06 25 (P. 237 107) Int. Cl8 A01N 57/10 Pierwszeństwof 81 06 27 Republika Federalna Niemiec URZĄD PATENTOWY Zgłoszenie ogłoszono: 83 02 28 PRL Opis patentowy opublikowano: .1987 10 15 Twórcy wynalazku: Miklos Ghyczy, Heinrich Osthoff, Eugen Etschen- berg Uprawniony z patentu: A. Nattermann und Cie GmbH, Kolonia (Republika Federalna Niemiec) Środek owadobójczy Przedmiotem wynalazku jest środek owadobój¬ kach o do 80%, gdy substancję owadobójczą lub czy. Na plantacjach roślin, liczne żyjące i ssące mieszaninę kilku substancji owadobójczych stosuje owady powodują poważne straty produkcyjne, się wespół z pewną substancją dodatkową będącą zwłaszcza w przypadku upraw bawełny, ryżu, zbóż, fosfolipidem. ziemniaków, owoców, warzyw i winorośli. Środek owadobójczy według wynalazku zawiera * Celem zwalczania owadów, podstawową sprawą jedną lub więcej substancji owadobójczych oraz jest obecnie stosowanie chemicznych środków owa¬ znane nośniki, rozcieńczalniki, rozpuszczalniki, pro- dobójczych. Niejednokrotnie konieczne jest stoso¬ pellenty yiub inne obojętne substancje pomocnicze, wanie chemicznych substancji owadobójczych w a cechą tego środka jest to, że zawiera jeden lub znacznych stężeniach, co w rezultacie staje się ło więcej fosfolipidów z grupy obejmującej fosfaty- źródłem toksycznych zanieczyszczeń otoczenia. Nie¬ dylocholinę, fosfatydyloetanoloaminę, N-acylofosfa- znaczna rozpuszczalność niektórych substancji owa¬ tydyloetanoloaminy, fosfatydyloinozyt, fosfatydylo- dobójczych, zwłaszcza w wodzie, powoduje ko¬ serynę, lizolecytynę, fosfatydyloglicerynę i uwodor¬ nieczność użycia toksycznych rozpuszczalników or¬ nione fosfatydylocholiny, przy czym stosunek wa¬ ganicznych. Ponadto większość chemicznych sub¬ 15 gowy substancji czynnej lub substancji czynnych stancji owadobójczych nie zawsze może wykazać do fosfolipidu lub fosfolipidów wynosi od 1 : 0,2 do swoją całkowitą aktywność, ponieważ nie wystar¬ 1 :20.
  • Insecticide Resistance in the Sugarcane Borer, Diatraea Saccharalis (F.)

    Insecticide Resistance in the Sugarcane Borer, Diatraea Saccharalis (F.)

    Louisiana State University LSU Digital Commons LSU Historical Dissertations and Theses Graduate School 1964 Insecticide Resistance in the Sugarcane Borer, Diatraea Saccharalis (F.). Raghunath Prasad Yadav Louisiana State University and Agricultural & Mechanical College Follow this and additional works at: https://digitalcommons.lsu.edu/gradschool_disstheses Recommended Citation Yadav, Raghunath Prasad, "Insecticide Resistance in the Sugarcane Borer, Diatraea Saccharalis (F.)." (1964). LSU Historical Dissertations and Theses. 965. https://digitalcommons.lsu.edu/gradschool_disstheses/965 This Dissertation is brought to you for free and open access by the Graduate School at LSU Digital Commons. It has been accepted for inclusion in LSU Historical Dissertations and Theses by an authorized administrator of LSU Digital Commons. For more information, please contact [email protected]. This dissertation has been 64—13,278 microfilmed exactly as received YADAV, Raghunath Prasad, 1935- INSECTICIDE RESISTANCE IN THE SUGARCANE SORER, DIATRAEA SACCHARALIS (F.). Louisiana State University, Ph.D., 1964 Zoology University Microfilms, Inc., Ann Arbor, Michigan INSECTICIDE RESISTANCE IN THE SUGARCANE BORER, DIATRAEA SACCHARALIS (F.) A Dissertation Submitted to the Graduate Faculty of the Louisiana State University and Agricultural and Mechanical College in partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Entomology by Raghunath Prasad Yadav M.S., Govt. Agricultural College, Kanpur, 1958 May, 1964 ACKNOWLEDGMENT The writer is sincerely grateful to his major professor, Dr. W. H. Long, for many helpful suggestions and assistance in the preparation of this manuscript. Special thanks are due Dr. L. D. Newsom, Head of the Department of Entomology, for providing the opportunity to study at Louisiana State University.
  • Identifying Potential POP and PBT Substances Development of a New Persistence/ Bioaccumulation Score

    Identifying Potential POP and PBT Substances Development of a New Persistence/ Bioaccumulation Score

    Identifying potential POP and PBT substances Development of a new Persistence/ Bioaccumulation score Report 601356001/2011 E. Rorije et al. National Insitute for Public Health and the Environment P.O. Box 1 | 3720 BA Bilthoven www.rivm.com Identifying potential POP and PBT substances Development of a new Persistence/Bioaccumulation-score RIVM Report 601356001/2011 Page 1 of 86 RIVM Report 601356001 Colophon © RIVM 2011 Parts of this publication may be reproduced, provided acknowledgement is given to the 'National Institute for Public Health and the Environment', along with the title and year of publication. E. Rorije (first author), SEC E.M.J. Verbruggen, SEC A. Hollander, LER T.P. Traas, SEC M.P.M. Janssen, SEC Contact: Martien Janssen RIVM/SEC [email protected] This investigation has been performed by order and for the account of I&M/RB, within the framework of Mondiaal Stoffenbeleid (M/601356) and REACH strategic support (M/601353) Page 2 of 86 RIVM Report 601356001 Abstract Identifying potential POP and PBT candidates Development of a new Persistence/Bioaccumulation score RIVM has screened the potential for long-term fate in the environment of a large number of substances. For this purpose a new methodology has been developed which indicates whether substances will persist in the environment and/or bioaccumulate in biological organisms. The results are a first step towards selection of substances which have inherent chemical properties that potentially make them a long-term hazard for the environment. Further research into the actual persistence and bioaccumulation of these substances in the environment will be needed.
  • NMP-Free Formulations of Neonicotinoids

    NMP-Free Formulations of Neonicotinoids

    (19) & (11) EP 2 266 400 A1 (12) EUROPEAN PATENT APPLICATION (43) Date of publication: (51) Int Cl.: 29.12.2010 Bulletin 2010/52 A01N 43/40 (2006.01) A01N 43/86 (2006.01) A01N 47/40 (2006.01) A01N 51/00 (2006.01) (2006.01) (2006.01) (21) Application number: 09305544.0 A01P 7/00 A01N 25/02 (22) Date of filing: 15.06.2009 (84) Designated Contracting States: (72) Inventors: AT BE BG CH CY CZ DE DK EE ES FI FR GB GR • Gasse, Jean-Jacques HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL 27600 Saint-Aubin-Sur-Gaillon (FR) PT RO SE SI SK TR • Duchamp, Guillaume Designated Extension States: 92230 Gennevilliers (FR) AL BA RS • Cantero, Maria 92230 Gennevilliers (FR) (71) Applicant: NUFARM 92233 Gennevelliers (FR) (74) Representative: Cabinet Plasseraud 52, rue de la Victoire 75440 Paris Cedex 09 (FR) (54) NMP-free formulations of neonicotinoids (57) The invention relates to NMP-free liquid formulation comprising at least one nicotinoid and at least one aprotic polar component selected from the group comprising the compounds of formula I, II or III below, and mixtures thereof, wherein R1 and R2 independently represent H or an alkyl group having less than 5 carbons, preferably a methyl group, and n represents an integer ranging from 0 to 5, and to their applications. EP 2 266 400 A1 Printed by Jouve, 75001 PARIS (FR) EP 2 266 400 A1 Description Technical Field of the invention 5 [0001] The invention relates to novel liquid formulations of neonicotinoids and to their use for treating plants, for protecting plants from pests and/or for controlling pests infestation.