CN101588719B - 基于唑并嘧啶基胺衍生物和杀虫剂的农药混合物 - Google Patents
基于唑并嘧啶基胺衍生物和杀虫剂的农药混合物 Download PDFInfo
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- 125000006340 pentafluoro ethyl group Chemical group FC(F)(F)C(F)(F)* 0.000 description 1
- 125000003538 pentan-3-yl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])[H] 0.000 description 1
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- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 1
- 230000029553 photosynthesis Effects 0.000 description 1
- 238000010672 photosynthesis Methods 0.000 description 1
- 230000035479 physiological effects, processes and functions Effects 0.000 description 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 description 1
- 150000004885 piperazines Chemical class 0.000 description 1
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- 239000002574 poison Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
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- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
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- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-N 0.000 description 1
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- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
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- 239000004550 soluble concentrate Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
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- 229940014213 spinosad Drugs 0.000 description 1
- DTDSAWVUFPGDMX-UHFFFAOYSA-N spirodiclofen Chemical compound CCC(C)(C)C(=O)OC1=C(C=2C(=CC(Cl)=CC=2)Cl)C(=O)OC11CCCCC1 DTDSAWVUFPGDMX-UHFFFAOYSA-N 0.000 description 1
- CLSVJBIHYWPGQY-GGYDESQDSA-N spirotetramat Chemical compound CCOC(=O)OC1=C(C=2C(=CC=C(C)C=2)C)C(=O)N[C@@]11CC[C@H](OC)CC1 CLSVJBIHYWPGQY-GGYDESQDSA-N 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
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- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- YROXIXLRRCOBKF-UHFFFAOYSA-N sulfonylurea Chemical class OC(=N)N=S(=O)=O YROXIXLRRCOBKF-UHFFFAOYSA-N 0.000 description 1
- XIUROWKZWPIAIB-UHFFFAOYSA-N sulfotep Chemical compound CCOP(=S)(OCC)OP(=S)(OCC)OCC XIUROWKZWPIAIB-UHFFFAOYSA-N 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 208000024891 symptom Diseases 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000012622 synthetic inhibitor Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- UJMBCXLDXJUMFB-GLCFPVLVSA-K tartrazine Chemical compound [Na+].[Na+].[Na+].[O-]C(=O)C1=NN(C=2C=CC(=CC=2)S([O-])(=O)=O)C(=O)C1\N=N\C1=CC=C(S([O-])(=O)=O)C=C1 UJMBCXLDXJUMFB-GLCFPVLVSA-K 0.000 description 1
- 235000012756 tartrazine Nutrition 0.000 description 1
- 239000004149 tartrazine Substances 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- FFSJPOPLSWBGQY-UHFFFAOYSA-N triazol-4-one Chemical compound O=C1C=NN=N1 FFSJPOPLSWBGQY-UHFFFAOYSA-N 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- RVKCCVTVZORVGD-UHFFFAOYSA-N trinexapac-ethyl Chemical group O=C1CC(C(=O)OCC)CC(=O)C1=C(O)C1CC1 RVKCCVTVZORVGD-UHFFFAOYSA-N 0.000 description 1
- SBXWFLISHPUINY-UHFFFAOYSA-N triphenyltin Chemical class C1=CC=CC=C1[Sn](C=1C=CC=CC=1)C1=CC=CC=C1 SBXWFLISHPUINY-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- DBXFMOWZRXXBRN-LWKPJOBUSA-N valifenalate Chemical compound CC(C)OC(=O)N[C@@H](C(C)C)C(=O)NC(CC(=O)OC)C1=CC=C(Cl)C=C1 DBXFMOWZRXXBRN-LWKPJOBUSA-N 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 238000009333 weeding Methods 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000005943 zeta-Cypermethrin Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- UHVMMEOXYDMDKI-JKYCWFKZSA-L zinc;1-(5-cyanopyridin-2-yl)-3-[(1s,2s)-2-(6-fluoro-2-hydroxy-3-propanoylphenyl)cyclopropyl]urea;diacetate Chemical compound [Zn+2].CC([O-])=O.CC([O-])=O.CCC(=O)C1=CC=C(F)C([C@H]2[C@H](C2)NC(=O)NC=2N=CC(=CC=2)C#N)=C1O UHVMMEOXYDMDKI-JKYCWFKZSA-L 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/02—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having no bond to a nitrogen atom
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/22—O-Aryl or S-Aryl esters thereof
Abstract
本发明涉及农药混合物,其包含:a)式(I)的唑并嘧啶基胺:其中各取代基如说明书所定义,和b)至少一种如本说明书中所定义的杀虫剂化合物II;植物保护混合物;含有这些混合物的组合物,以及涉及通过将这些混合物施用于植物或其场所来防治或预防植物中的真菌侵染或有害昆虫或线虫的方法和改善植物的健康的方法。
Description
本发明涉及农药混合物,其包含:
a)至少一种式I的唑并嘧啶基胺:
其中各取代基如下所定义:
R1为C3-C12烷基、C2-C12链烯基、C5-C12烷氧基烷基、C3-C6环烷基、苯基或苯基-C1-C4烷基;
R2为C1-C12烷基、C2-C12链烯基、C1-C4卤代烷基或C1-C4烷氧基-C1-C4烷基,
其中R1和/或R2中的脂族链可被1-4个相同或不同的Ra基团取代:
Ra为卤素、氰基、羟基、巯基、C1-C10烷基、C1-C10卤代烷基、C3-C8环烷基、C2-C10链烯基、C2-C10炔基、C1-C6烷氧基、C1-C6烷硫基、C1-C6烷氧基-C1-C6烷基或NRARB;
RA、RB为氢或C1-C6烷基;
其中R1和/或Ra中的环状基团可被1-4个Rb基团取代:
Rb为卤素、氰基、羟基、巯基、硝基、NRARB、C1-C10烷基、C1-C6卤代烷基、C2-C6链烯基、C2-C6炔基或C1-C6烷氧基;
R3为氢、卤素、氰基、NRARB、羟基、巯基、C1-C6烷基、C1-C6卤代烷基、C3-C8环烷基、C1-C6烷氧基、C1-C6烷硫基、C3-C8环烷氧基、C3-C8环烷硫基、羧基、甲酰基、C1-C10烷基羰基、C1-C10烷氧基羰基、C2-C10链烯氧基羰基、C2-C10炔氧基羰基、苯基、苯氧基、苯硫基、苄氧基、苄硫基或C1-C6烷基-S(O)m-;
m为0、1或2;
A为CH或N;
和
b)至少一种化合物II,其选自下组:
A.1.有机(硫代)磷酸酯类:高灭磷(acephate)、唑啶磷(azamethiphos)、乙基谷硫磷(azinphos-ethyl)、谷硫磷(azinphos-methyl)、壤虫氯磷(chlorethoxyfos)、毒虫畏(chlorfenvinphos)、氯甲磷(chlormephos)、毒死蜱(chlorpyrifos)、甲基毒死蜱(chlorpyrifos-methyl)、蝇毒磷(coumaphos)、杀螟腈(cyanophos)、甲基内吸磷(demeton-S-methyl)、二嗪农(diazinon)、敌敌畏(dichlorvos/DDVP)、百治磷(dicrotophos)、乐果(dimethoate)、甲基毒虫畏(dimethylvinphos)、乙拌磷(disulfoton)、苯硫磷(EPN)、乙硫磷(ethion)、灭克磷(ethoprophos)、氨磺磷(famphur)、克线磷(fenamiphos)、杀螟松(fenitrothion)、倍硫磷(fenthion)、吡氟硫磷(flupyrazophos)、噻唑酮磷(fosthiazate)、庚虫磷(hepten ophos)、异噁唑磷(isoxathion)、马拉硫磷(malathion)、灭蚜磷(mecarbam)、甲胺磷(methamidophos)、杀扑磷(methidathion)、速灭磷(mevinphos)、久效磷(monocrotophos)、二溴磷(naled)、氧化乐果(omethoate)、砜吸磷(oxydemeton-methyl)、一六零五(parathion)、甲基一六零五(parathion-methyl)、稻丰散(phenthoate)、甲拌磷(phorate)、伏杀磷(phosalone)、亚胺硫磷(phosmet)、磷胺(phosphamidon)、辛硫磷(phoxim)、虫螨磷(pirimiphos-methyl)、丙溴磷(profenofos)、烯虫磷(propetamphos)、丙硫磷(prothiofos)、吡唑硫磷(pyraclofos)、打杀磷(pyridaphenthion)、喹恶磷(quinalphos)、硫特普(sulfotep)、嘧丙磷(tebupirimfos)、硫甲双磷(temephos)、特丁磷(terbufos)、杀虫畏(tetrachlorvinphos)、甲基乙拌磷(thiometon)、三唑磷(triazophos)、敌百虫(trichlorfon)、蚜灭多(vamidothion);
A.2.氨基甲酸酯类:涕灭威(aldicarb)、棉铃威(alanycarb)、噁虫威(bendiocarb)、丙硫克百威(benfuracarb)、丁叉威(butocarboxim)、氧丁叉威(butoxycarboxim)、甲萘威(carbaryl)、虫螨威(carbofuran)、丁硫克百威(carbosulfan)、苯虫威(ethiofencarb)、丁苯威(fenobucarb)、伐虫脒(formetanate)、呋线威(furathiocarb)、异丙威(isoprocarb)、灭虫威(methiocarb)、灭多虫(methomyl)、速灭威(metolcarb)、甲氨叉威(oxamyl)、抗蚜威(pirimicarb)、残杀威(propoxur)、硫双威(thiodicarb)、特氨叉威(thiofanox)、混杀威(trimethacarb)、二甲威(XMC)、灭杀威(xylylcarb)、唑蚜威(triazamate);
A.3.合成除虫菊酯类:氟锁草醚(acifluorfen)、丙烯除虫菊(allethrin)、d-顺-反丙烯除虫菊、d-反丙烯除虫菊、氟氯菊酯(bifenthrin)、反丙烯除虫菊(bioallethrin)、反丙烯除虫菊S-环戊烯基(bioallethrin S-cylclopentenyl)、右旋反灭虫菊酯(bioresmethrin)、乙氰菊脂(cycloprothrin)、氟氯氰菊酯(cyfluthrin)、β-氟氯氰菊酯、(RS)氯氟氰菊酯(cyhalothrin)、λ-(RS)氯氟氰菊酯、γ-(RS)氯氟氰菊酯、氯氰菊酯(cypermethrin)、甲体氯氰菊酯(alpha-cypermethrin)、乙体氯氰菊酯(beta-cypermethrin)、辛体氯氰菊酯(beta-cypermethrin)、己体氯氰菊酯(zeta-cypermethrin)、苯醚氰菊酯(cyphenothrin)、溴氰菊酯(deltamethrin)、烯炔菊酯(empenthrin)、高氰戊菊酯(esfenvalerate)、醚菊酯(etofenprox)、甲氰菊酯(fenpropathrin)、杀灭菊酯(fenvalerate)、氟氰戊菊酯(flucythrinate)、氟氯苯菊酯(flumethrin)、T-氟氯苯菊酯(tau-flumethrin)、卤醚菊酯(halfenprox)、咪炔菊酯(imiprothrin)、氯菊酯(permethrin)、苯醚菊酯(phenothrin)、炔酮菊酯(prallethrin)、灭虫菊(resmethrin)、RU 15525、灭虫硅醚(silafluofen)、七氟菊酯(tefluthrin)、胺菊酯(tetramethrin)、四溴菊酯(tralomethrin)、四氟菊酯(transfluthrin);ZXI 8901;
A.4.拟保幼激素(juvenile hormone mimics):蒙五一二(hydroprene)、蒙七七七(kinoprene)、蒙五一五(methoprene)、双氧威(fenoxycarb)、蚊蝇醚(pyriproxyfen);
A.5.烟碱受体激动剂/拮抗剂化合物:吡虫清(acetamiprid)、杀虫磺(bensultap)、巴丹(cartap hydrochloride)、噻虫胺(clothianidin)、呋虫胺(dinotefuran)、吡虫啉(imidacloprid)、噻虫嗪(thiamethoxam)、硝胺烯啶(nitenpyram)、烟碱(nicotine)、艾克敌105(spinosad)(变构激动剂)、噻虫啉(thiacloprid)、硫环杀(thiocyclam)、杀虫双(thiosultap-sodium)和式Γ1的噻唑化合物:
A.6.GABA门控氯离子通道拮抗剂化合物:氯丹(chlordane)、硫丹(endosulfan)、林丹(gamma-HCH)、acetoprole、乙虫清(ethiprole)、锐劲特(fipronil)、pyrafluprole、pyriprole、氟吡唑虫(vaniliprole)、5-氨基-1-(2,6-二氯-4-三氟甲基苯基)-4-三氟甲烷亚磺酰基-1H-吡唑-3-甲酰胺;
A.7.氯离子通道活化剂:齐墩螨素(abamectin)、甲氨基阿维菌素(emamectin benzoate)、米尔螨素(milbemectin)、lepimectin;
A.8.METI I化合物:喹螨醚(fenazaquin)、唑螨酯(fenpyroximate)、嘧胺苯醚(pyrimidifen)、哒螨酮(pyridaben)、吡螨胺(tebufenpyrad)、唑虫酰胺(tolfenpyrad)、flufenerim、鱼藤酮(rotenone);
A.9.METI II和III化合物:灭螨醌(acequinocyl)、fluacyprim、灭蚁腙(hydramethylnon);
A.10.氧化磷酸化去偶剂(Uncoupler):氟唑虫清(chlorfenapyr),二硝甲酚(DNOC);
A.11.氧化磷酸化抑制剂:唑环锡(azocyclotin)、三环锡(cyhexatin)、杀螨硫隆(diafenthiuron)、杀螨锡(fenbutatin oxide)、克螨特(propargite)、三氯杀螨砜(tetradifon);
A.12.蜕皮干扰剂(Moulting disruptor):cryomazine、chromafenozide、特丁苯酰肼(halofenozide)、甲氧苯酰肼(methoxyfenozide)、双苯酰肼(tebufenozide);
A.13.增效剂:增效醚(piperonyl butoxide)、脱叶磷(tribufos);
A.14.钠通道阻断剂化合物:噁二唑虫(indoxacarb)、氰氟虫胺(metaflumizone);
A.15.熏蒸剂:甲基溴、氯化苦(chloropicrin)、磺酰氟(sulfuryl fluoride)
A.16.选择性进食阻断剂(Selective feeding blocker):氟铝酸钠(cryolite)、拒嗪酮(pymetrozine)、氟啶虫酰胺(flonicamid);
A.17.螨虫生长抑制剂:四螨嗪(clofentezine)、噻螨酮(hexythiazox)、特苯噁唑(etoxazole);
A.18.甲壳素合成抑制剂:噻嗪酮(buprofezin)、双三氟虫脲(bistrifluron)、定虫隆(chlorfluazuron)、氟脲杀(diflubenzuron)、氟螨脲(flucycloxuron)、氟虫脲(flufenoxuron)、氟铃脲(hexaflumuron)、氟丙氧脲(lufenuron)、双苯氟脲(novaluron)、多氟脲(noviflumuron)、伏虫隆(teflubenzuron)、杀虫隆(triflumuron);
A.19.类脂生物合成抑制剂:螺螨酯(spirodiclofen)、螺甲螨酯(spiromesifen)、spirotetramat;
A.20.章鱼胺激动剂(octapaminergic agonist):虫螨脒(amitraz);
A.21.鱼尼汀(ryanodine)受体调节剂:氟虫酰胺(flubendiamide);
A.22.其它:磷化铝、amidoflumet、benclothiaz、苯螨特(benzoximate)、联苯肼酯(bifenazate)、硼砂、溴螨酯(bromopropylate)、氰化物、cyenopyrafen、丁氟螨酯(cyflumetofen)、灭螨猛(chinomethionate)、开乐散(dicofol)、氟乙酸酯、膦、啶虫丙醚(pyridalyl)、pyrifluquinazon、硫、吐酒石(tartar emetic);
A.23.N-R′-2,2-二halo-1-R″环丙烷甲酰胺-2-(2,6-二氯-α,α,α-三氟-对甲苯基)腙或N-R′-2,2-二(R′″)丙酰胺-2-(2,6-二氯-α,α,α-三氟-对甲苯基)-腙,其中R′为甲基或乙基,halo为氯或溴,R″为氢或甲基且R′″为甲基或乙基;
A.24.丙二腈化合物:CF3(CH2)2C(CN)2CH2(CF2)3CF2H、CF3(CH2)2C(CN)2CH2(CF2)5CF2H、CF3(CH2)2C(CN)2(CH2)2C(CF3)2F、CF3(CH2)2C(CN)2(CH2)2(CF2)3CF3、CF2H(CF2)3CH2C(CN)2CH2(CF2)3CF2H、CF3(CH2)2C(CN)2CH2(CF2)3CF3、CF3(CF2)2CH2C(CN)2CH2(CF2)3CF2H和CF3CF2CH2C(CN)2CH2(CF2)3CF2H;
A.25.微生物干扰物(disruptor):苏云金芽孢杆菌以色列亚种(Bacillusthuringiensis subsp.Israelensi)、球形芽孢杆菌(Bacillus sphaericus)、苏云金芽胞杆菌鲇泽亚种(Bacillus thuringiensis subsp.Aizawai)、苏云金芽孢杆菌库斯克亚种(Bacillus thuringiensis subsp.Kurstaki)、苏云金芽胞杆菌拟步行甲亚种(Bacillus thuringiensis subsp.Tenebrionis)。
本发明还涉及植物保护混合物且涉及一种通过将所述混合物施用于植物或其场所来改善所述植物的健康的方法。
此外,本发明涉及一种防治真菌和/或改善植物健康的方法,其包括用本发明混合物中所存在的农药以任何所需顺序或同时,即联合或分开对真菌侵染或易受真菌侵染的位置,例如植物或植物繁殖材料进行处理。
此外,本发明涉及一种防治有害昆虫或线虫的方法,其包括用本发明混合物中所存在的农药以任何所需顺序或同时,即联合或分开对被所述害虫侵染或易被所述害虫侵染的位置,例如植物或植物繁殖材料进行处理。
在害虫防治领域产生的一个典型问题是需要降低活性成分的剂量率以降低或避免不利的环境或毒性作用,同时仍允许有效防治害虫和病原体。
所遇到的另一问题是需要能够得到对宽范围的害虫和病原体有效的害虫防治剂。
本发明的另一问题是需要改善植物的组合物,一种改善在下文中通常称为“植物健康”的方法。例如可提及的有利性能为改善包括如下的作物特征:萌发、作物产量、蛋白质含量、油含量、淀粉含量、更发达的根系(改善根的生长)、改善的胁迫耐受性(例如对干旱、热、盐、UV、水、寒冷)、乙烯减少(降低产生和/或抑制接收)、分蘖增加、植物高度增加、叶片变大、死亡的基生叶更少、更强的分蘖、叶颜色更绿、色素含量、光合作用活性、需要更少的投入(如肥料和水)、需要更少的种子、更能生产的分蘖、较早开花、谷物更早成熟、更少的植物寄生、枝生长增加、植物活力增加、植物直立增加和早期更好发芽;或本领域熟练技术人员熟知的任何其它优点。
与使用农药相关的另一困难在于反复和单一施用单独的活性化合物在很多情况下导致害虫或病原体出现快速的选择性,这些害虫或病原体对于所述活性化合物具有天然的或者适应的耐药性。
因此,本发明的目的是提供解决上述问题的农药混合物。
对抗有害的植物病原性真菌并不是农民必须面对的唯一问题。有害昆虫和其它害虫也可对作物和其它植物造成很大的损害。希望杀真菌和杀虫活性有效组合以克服该问题。因此,本发明的另一目的是提供一方面具有良好杀真菌活性且另一方面具有良好杀虫活性并导致更宽的农药活性谱的混合物。
我们发现该目的部分或全部由开头所定义的活性化合物的组合实现。
并且在施用至植物、植物部分、种子或它们生长的场所时,与单个化合物的防治率相比,如本文开头所定义的至少一种式I化合物与至少一种化合物II的混合物对植物病原体显示出显著增强作用和/或更适合改善植物健康。
已发现,本发明混合物(例如如开头所定义的式I化合物与化合物II的混合物)的作用远远超过单独存在于混合物中的活性化合物的杀真菌和杀虫作用。已表明,在本发明的框架内所述混合物显示植物健康作用。术语植物健康包括各种与害虫防治无关的对于植物的改善。
上文称作组分a的式I的唑并嘧啶-7-基胺,其制备及其对有害真菌的作用由如下文献已知(EP-A 71 792;EP-A 141 317;WO 03/009687;WO05/087771;WO 05/087772;WO 05/087773;PCT/EP/05/002426;PCT/EP2006/050922;PCT/EP 2006/060399)。
组A.1-A.25的市售化合物II可在The Pesticide Manual,第13版,British Crop Protection Council(2003)在其它出版物,如http://www.hclrss.demon.co.uk/index.html中找到。
5-氨基-1-(2,6-二氯-4-三氟甲基-苯基)-4-三氯甲烷亚磺酰基-1H-吡唑-3-硫代甲酸酰胺及其制备已描述于WO 98/28279中。Lepimectin由AgroProject,PJB Publications Ltd,2004年11月已知。Benclothiaz及其制备描述于EP-A1454621中。杀扑磷和对氧磷及其制备描述于Farm ChemicalsHandbook,第88卷,Meister Publishing Company,2001中。Acetoprole及其制备描述于WO 98/28277中。氰氟虫胺及其制备描述于EP-A1462456中。吡氟硫磷描述于Pesticide Science 54,1988,第237-243页和US 4822779中。Pyrafluprole及其制备描述于JP 2002193709和WO 01/00614中。Pyriprole及其制备描述于WO 98/45274和US 6335357中。Amidoflumet及其制备描述于US 6221890和JP 21010907中。Flufenerim及其制备描述于WO 03/007717和WO 03/007718中。类似于AKD-1022的新烟碱类的制备方法已由Zhang,A.等人描述于J.Neurochemistry,75(3),2000中。丁氟螨酯及其制备描述于WO 04/080180中。丙二腈化合物CF3(CH2)2C(CN)2CH2(CF2)3CF2H、CF3(CH2)2C(CN)2CH2(CF2)5CF2H、CF3(CH2)2C(CN)2(CH2)2C(CF3)2F、CF3(CH2)2C(CN)2(CH2)2(CF2)3CF3、CF2H(CF2)3CH2C(CN)2CH2(CF2)3CF2H、CF3(CH2)2C(CN)2CH2(CF2)3CF3、CF3(CF2)2CH2C(CN)2CH2(CF2)3CF2H和CF3CF2CH2C(CN)2CH2(CF2)3CF2H已描述于WO 05/63694中。
在对上文各式给出的符号定义中,使用通常表示以下取代基的集合性术语:
卤素:氟、氯、溴和碘;
烷基:具有1至4、6、8或10个碳原子的饱和直链或支化烃基,例如C1-C6烷基,如甲基、乙基、丙基、1-甲基乙基、丁基、1-甲基丙基、2-甲基丙基、1,1-二甲基乙基、戊基、1-甲基丁基、2-甲基丁基、3-甲基丁基、2,2-二甲基丙基、1-乙基丙基、己基、1,1-二甲基丙基、1,2-二甲基丙基、1-甲基戊基、2-甲基戊基、3-甲基戊基、4-甲基戊基、1,1-二甲基丁基、1,2-二甲基丁基、1,3-二甲基丁基、2,2-二甲基丁基、2,3-二甲基丁基、3,3-二甲基丁基、1-乙基丁基、2-乙基丁基、1,1,2-三甲基丙基、1,2,2-三甲基丙基、1-乙基-1-甲基丙基和1-乙基-2-甲基丙基;
卤代烷基:具有1至2、4或6个碳原子的直链或支化烷基(如上所述),其中这些基团中的一些或所有氢原子可被上述卤素原子替换:尤其是C1-C2卤代烷基,如氯甲基、溴甲基、二氯甲基、三氯甲基、氟甲基、二氟甲基、三氟甲基、氯氟甲基、二氯氟甲基、氯二氟甲基、1-氯乙基、1-溴乙基、1-氟乙基、2-氟乙基、2,2-二氟乙基、2,2,2-三氟乙基、2-氯-2-氟乙基、2-氯-2,2-二氟乙基、2,2-二氯-2-氟乙基、2,2,2-三氯乙基、五氟乙基或1,1,1-三氟丙-2-基。
鉴于本发明中式I的唑并嘧啶基胺的意欲用途,特别优选取代基在每种情况下单独或组合地具有以下含义:
根据本发明特别适合使用的是如下式I的化合物,其中R1为可被1至3个卤素或C1-C4烷基取代的直链或支化C3-C12烷基或苯基。
在式I化合物的一个实施方案中,Ra基团不存在。
优选实施方案涉及如下式I的化合物,其中R1为直链或支化C5-C10烷基,尤其是乙基、3,5,5-三甲基己基、正庚基、正辛基、正壬基和正癸基。
另一实施方案涉及如下式I的化合物,其中R1为未被取代或被1至4个卤素、氰基、羟基、巯基、硝基、NRARB、C1-C10烷基、C1-C6卤代烷基、C2-C6链烯基、C2-C6炔基和C1-C6烷氧基取代的苯基。
优选的式I化合物为其中R1为对应于G基团的取代苯基的那些:
其中
L1为氰基、卤素、羟基、巯基、硝基、NRARB、C1-C10烷基、C1-C6卤代烷基、C2-C6链烯基、C2-C6炔基和C1-C6烷氧基;和
L2、L3相互独立地为氢或在L1下所提及的基团之一,且
#表示连接至唑并嘧啶骨架的键。
在式I化合物的另一实施方案中,L1为氰基、卤素、羟基、巯基、硝基、NRARB、C1-C6烷基、卤代甲基或C1-C2烷氧基,优选为氰基、卤素、C1-C6烷基、卤代甲基或C1-C2烷氧基。
在式I化合物的另一实施方案中,L2为氢或上述基团之一。
在式I化合物的另一实施方案中,L3为氢、氰基、卤素、羟基、巯基、硝基、NRARB、C1-C6烷基、卤代甲基或C1-C2烷氧基,优选为氢。
优选其中R2为直链或支化C1-C12烷基、C1-C4烷氧基-C1-C4烷基或C1-C4卤代烷基的式I的化合物。
在式I化合物的特别优选实施方案中,R2为甲基、乙基、正丙基、正辛基、三氟甲基或甲氧基甲基,尤其是甲基、乙基、三氟甲基或甲氧基甲基。
此外,优选为如下式I的化合物,其中R3为氢。
在式I化合物的另一实施方案中,R3为氨基。
式I化合物的一个实施方案涉及A为N的那些。这些化合物对应于式IA,其中变量如对式I所定义:
式I化合物的另一实施方案涉及A为CH的那些。这些化合物对应于式IB,其中变量如对式I所定义:
在优选化合物I的另一实施方案中,R1与R2的碳链一起不具有超过12个的碳原子。
鉴于化合物的用途,尤其优选汇集于下表中的化合物I。此外,表中关于取代基所提及的基团本身(与其中提及它们的组合无关)为所述取代基的特别优选实施方案。
表1
其中对化合物而言R1、R2和R3的组合在每种情况下对应于表I的一行的式IA的化合物
表2
其中对化合物而言R1、R2和R3的组合在每种情况下对应于表I的一行的式IB的化合物
表I
编号 | R1 | R2 | R3 |
I-1 | C6H5 | CH3 | H |
I-2 | 2-Cl-C6H4 | CH3 | H |
I-3 | 3-Cl-C6H4 | CH3 | H |
I-4 | 4-Cl-C6H4 | CH3 | H |
I-5 | 2-F-C6H4 | CH3 | H |
I-6 | 3-F-C6H4 | CH3 | H |
I-7 | 4-F-C6H4 | CH3 | H |
I-8 | 2,4-Cl2-C6H3 | CH3 | H |
I-9 | 3,4-Cl2-C6H3 | CH3 | H |
I-10 | 2,4-F2-C6H3 | CH3 | H |
编号 | R1 | R2 | R3 |
I-11 | 3,4-F2-C6H3 | CH3 | H |
I-12 | 4-CH3-C6H4 | CH3 | H |
I-13 | 4-CH2CH3-C6H4 | CH3 | H |
I-14 | 4-CH2CH2CH3-C6H4 | CH3 | H |
I-15 | 4-CH(CH3)2-C6H4 | CH3 | H |
I-16 | 4-CH2CH2CH2CH3-C6H4 | CH3 | H |
I-17 | 4-C(CH3)CH2CH3-C6H4 | CH3 | H |
I-18 | 4-C(CH3)3-C6H4 | CH3 | H |
I-19 | CH2CH2CH2CH3 | CH3 | H |
I-20 | CH2CH2CH2CH2CH3 | CH3 | H |
I-21 | CH2CH2CH2CH2CH2CH3 | CH3 | H |
I-22 | CH2CH(CH3)CH2CH2CH3 | CH3 | H |
I-23 | CH2CH(CH2CH3)2 | CH3 | H |
I-24 | CH2CH2CH2CH2CH2CH2CH3 | CH3 | H |
I-25 | CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | H |
I-26 | CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | H |
I-27 | CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | H |
I-28 | CH2CH2CH(CH3)CH2CH(CH3)3 | CH3 | H |
I-29 | CH2CH2CH2CH3 | CH3 | NH2 |
I-30 | CH2CH2CH2CH2CH3 | CH3 | NH2 |
I-31 | CH2CH2CH2CH2CH2CH3 | CH3 | NH2 |
I-32 | CH2CH(CH3)CH2CH2CH3 | CH3 | NH2 |
I-33 | CH2CH(CH2CH3)2 | CH3 | NH2 |
I-34 | CH2CH2CH2CH2CH2CH2CH3 | CH3 | NH2 |
I-35 | CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | NH2 |
I-36 | CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | NH2 |
I-37 | CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | NH2 |
I-38 | CH2CH2CH(CH3)CH2CH(CH3)3 | CH3 | NH2 |
I-39 | CH2CH2CH2CH3 | CH3 | CH3 |
I-40 | CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-4I | CH2CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-42 | CH2CH(CH3)CH2CH2CH3 | CH3 | CH3 |
I-43 | CH2CH(CH2CH3)2 | CH3 | CH3 |
I-44 | CH2CH2CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-45 | CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-46 | CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | CH3 |
编号 | R1 | R2 | R3 |
I-47 | CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-48 | CH2CH2CH(CH3)CH2CH(CH3)3 | CH3 | CH3 |
I-49 | (CH2)3-O-CH3 | CH3 | H |
I-50 | (CH2)3-O-CH2CH3 | CH3 | H |
I-51 | (CH2)3-O-CH2CH2CH3 | CH3 | H |
I-52 | (CH2)3-O-CH2CH2CH2CH3 | CH3 | H |
I-53 | (CH2)3-O-CH2CH2CH2CH2CH3 | CH3 | H |
I-54 | (CH2)3-O-CH2CH2CH2CH2CH2CH3 | CH3 | H |
I-55 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH3 | CH3 | H |
I-56 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | H |
I-57 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | H |
I-58 | (CH2)3-O-CH(CH3)2 | CH3 | H |
I-59 | (CH2)3-O-C(CH3)3 | CH3 | H |
I-60 | (CH2)3-O-CH2C(CH3)3 | CH3 | H |
I-61 | (CH2)3-O-CH(CH3)CH2C(CH3)3 | CH3 | H |
I-62 | (CH2)3-O-CH(CH2CH3)CH2C(CH3)3 | CH3 | H |
I-63 | (CH2)3-O-CH2CH(CH3)CH2CH(CH3)2 | CH3 | H |
I-64 | (CH2)3-O-CH2CH(CH2CH3)CH2CH2CH3 | CH3 | H |
I-65 | (CH2)3-O-CH2CH2CH(CH3)CH2CH(CH3)2 | CH3 | H |
I-66 | (CH2)3-O-CH2CH2CH(CH3)CH2C(CH3)3 | CH3 | H |
I-67 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH(CH3)2 | CH3 | H |
I-68 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH2CH(CH3)2 | CH3 | H |
I-69 | (CH2)3-O-CH3 | CH3 | CH3 |
I-70 | (CH2)3-O-CH2CH3 | CH3 | CH3 |
I-71 | (CH2)3-O-CH2CH2CH3 | CH3 | CH3 |
I-72 | (CH2)3-O-CH2CH2CH2CH3 | CH3 | CH3 |
I-73 | (CH2)3-O-CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-74 | (CH2)3-O-CH2CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-75 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-76 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-77 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH3 | CH3 |
I-78 | (CH2)3-O-CH(CH3)2 | CH3 | CH3 |
I-79 | (CH2)3-O-C(CH3)3 | CH3 | CH3 |
I-80 | (CH2)3-O-CH2C(CH3)3 | CH3 | CH3 |
I-81 | (CH2)3-O-CH(CH3)CH2C(CH3)3 | CH3 | CH3 |
I-82 | (CH2)3-O-CH(CH2CH3)CH2C(CH3)3 | CH3 | CH3 |
编号 | R1 | R2 | R3 |
I-83 | (CH2)3-O-CH2CH(CH3)CH2CH(CH3)2 | CH3 | CH3 |
I-84 | (CH2)3-O-CH2CH(CH2CH3)CH2CH2CH3 | CH3 | CH3 |
I-85 | (CH2)3-O-CH2CH2CH(CH3)CH2CH(CH3)2 | CH3 | CH3 |
I-86 | (CH2)3-O-CH2CH2CH(CH3)CH2C(CH3)3 | CH3 | CH3 |
I-87 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH(CH3)2 | CH3 | CH3 |
I-88 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH2CH(CH3)2 | CH3 | CH3 |
I-89 | CH2-C6H5 | CF3 | H |
I-90 | CH2-(4-Cl-C6H4) | CF3 | H |
I-91 | CH2CH2CH3 | CF3 | H |
I-92 | CH2CH2CH2CH3 | CF3 | H |
I-93 | CH2CH2CH2CH2CH3 | CF3 | H |
I-94 | CH2CH2CH2CH2CH2CH3 | CF3 | H |
I-95 | CH2CH(CH3)CH2CH2CH3 | CF3 | H |
I-96 | CH2CH(CH2CH3)2 | CF3 | H |
I-97 | CH2CH2CH2CH2CH2CH2CH3 | CF3 | H |
I-98 | CH2CH2CH2CH2CH2CH2CH2CH3 | CF3 | H |
I-99 | CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CF3 | H |
I-100 | CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CF3 | H |
I-101 | CH2CH2CH(CH3)CH2CH(CH3)3 | CF3 | H |
I-102 | 环-C5H9 | CF3 | H |
I-103 | 环-C6H11 | CF3 | H |
I-104 | CH2CH2CH2CH3 | CH2CH3 | H |
I-105 | CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-106 | CH2CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-107 | CH2CH(CH3)CH2CH2CH3 | CH2CH3 | H |
I-108 | CH2CH(CH2CH3)2 | CH2CH3 | H |
I-109 | CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-110 | CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-111 | CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-112 | CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-113 | CH2CH2CH(CH3)CH2CH(CH3)3 | CH2CH3 | H |
I-114 | CH2CH2CH2CH3 | CH2CH3 | NH2 |
I-115 | CH2CH2CH2CH2CH3 | CH2CH3 | NH2 |
I-116 | CH2CH2CH2CH2CH2CH3 | CH2CH3 | NH2 |
I-117 | CH2CH(CH3)CH2CH2CH3 | CH2CH3 | NH2 |
I-118 | CH2CH(CH2CH3)2 | CH2CH3 | NH2 |
编号 | R1 | R2 | R3 |
I-119 | CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | NH2 |
I-120 | CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | NH2 |
I-121 | CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | NH2 |
I-122 | CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | NH2 |
I-123 | CH2CH2CH(CH3)CH2CH(CH3)3 | CH2CH3 | NH2 |
I-124 | CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-125 | CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-126 | CH2CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-127 | CH2CH(CH3)CH2CH2CH3 | CH2CH3 | CH3 |
I-128 | CH2CH(CH2CH3)2 | CH2CH3 | CH3 |
I-129 | CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-130 | CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-131 | CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-132 | CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-133 | CH2CH2CH(CH3)CH2CH(CH3)3 | CH2CH3 | CH3 |
I-134 | (CH2)3-O-CH3 | CH2CH3 | H |
I-135 | (CH2)3-O-CH2CH3 | CH2CH3 | H |
I-136 | (CH2)3-O-CH2CH2CH3 | CH2CH3 | H |
I-137 | (CH2)3-O-CH2CH2CH2CH3 | CH2CH3 | H |
I-138 | (CH2)3-O-CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-139 | (CH2)3-O-CH2CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-140 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-141 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-142 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | H |
I-143 | (CH2)3-O-CH(CH3)2 | CH2CH3 | H |
I-144 | (CH2)3-O-C(CH3)3 | CH2CH3 | H |
I-145 | (CH2)3-O-CH2C(CH3)3 | CH2CH3 | H |
I-146 | (CH2)3-O-CH(CH3)CH2C(CH3)3 | CH2CH3 | H |
I-147 | (CH2)3-O-CH(CH2CH3)CH2C(CH3)3 | CH2CH3 | H |
I-148 | (CH2)3-O-CH2CH(CH3)CH2CH(CH3)2 | CH2CH3 | H |
I-149 | (CH2)3-O-CH2CH(CH2CH3)CH2CH2CH3 | CH2CH3 | H |
I-150 | (CH2)3-O-CH2CH2CH(CH3)CH2CH(CH3)2 | CH2CH3 | H |
I-151 | (CH2)3-O-CH2CH2CH(CH3)CH2C(CH3)3 | CH2CH3 | H |
I-152 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH(CH3)2 | CH2CH3 | H |
I-153 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH2CH(CH3)2 | CH2CH3 | H |
I-154 | (CH2)3-O-CH3 | CH2CH3 | CH3 |
编号 | R1 | R2 | R3 |
I-155 | (CH2)3-O-CH2CH3 | CH2CH3 | CH3 |
I-156 | (CH2)3-O-CH2CH2CH3 | CH2CH3 | CH3 |
I-157 | (CH2)3-O-CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-158 | (CH2)3-O-CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-159 | (CH2)3-O-CH2CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-160 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-161 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-162 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH3 | CH3 |
I-163 | (CH2)3-O-CH(CH3)2 | CH2CH3 | CH3 |
I-164 | (CH2)3-O-C(CH3)3 | CH2CH3 | CH3 |
I-165 | (CH2)3-O-CH2C(CH3)3 | CH2CH3 | CH3 |
I-166 | (CH2)3-O-CH(CH3)CH2C(CH3)3 | CH2CH3 | CH3 |
I-167 | (CH2)3-O-CH(CH2CH3)CH2C(CH3)3 | CH2CH3 | CH3 |
I-168 | (CH2)3-O-CH2CH(CH3)CH2CH(CH3)2 | CH2CH3 | CH3 |
I-169 | (CH2)3-O-CH2CH(CH2CH3)CH2CH2CH3 | CH2CH3 | CH3 |
I-170 | (CH2)3-O-CH2CH2CH(CH3)CH2CH(CH3)2 | CH2CH3 | CH3 |
I-171 | (CH2)3-O-CH2CH2CH(CH3)CH2C(CH3)3 | CH2CH3 | CH3 |
I-172 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH(CH3)2 | CH2CH3 | CH3 |
I-173 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH2CH(CH3)2 | CH2CH3 | CH3 |
I-174 | CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-175 | CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-176 | CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-177 | CH2CH(CH3)CH2CH2CH3 | CH2CH2CH3 | H |
I-178 | CH2CH(CH2CH3)2 | CH2CH2CH3 | H |
I-179 | CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-180 | CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-181 | CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-182 | CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-183 | CH2CH2CH(CH3)CH2CH(CH3)3 | CH2CH2CH3 | H |
I-184 | CH2-O-CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-185 | CH2-O-CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-186 | CH2-O-CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-187 | CH2-O-CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-188 | CH2-O-CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-189 | CH2-O-CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-190 | CH2-O-C(CH3)3 | CH2CH2CH3 | H |
编号 | R1 | R2 | R3 |
I-191 | CH2-O-CH2C(CH3)3 | CH2CH2CH3 | H |
I-192 | CH2-O-CH(CH3)CH2C(CH3)3 | CH2CH2CH3 | H |
I-193 | CH2-O-CH(CH2CH3)CH2C(CH3)3 | CH2CH2CH3 | H |
I-194 | CH2-O-CH2CH(CH3)CH2CH(CH3)2 | CH2CH2CH3 | H |
I-195 | CH2-O-CH2CH(CH2CH3)CH2CH2CH3 | CH2CH2CH3 | H |
I-196 | CH2-O-CH2CH2CH(CH3)CH2CH(CH3)2 | CH2CH2CH3 | H |
I-197 | CH2-O-CH2CH2CH(CH3)CH2C(CH3)3 | CH2CH2CH3 | H |
I-198 | CH2-O-CH2CH2CH(CH3)CH2CH2CH(CH3)2 | CH2CH2CH3 | H |
I-199 | CH2-O-CH2CH2CH(CH3)CH2CH2CH2CH(CH3)2 | CH2CH2CH3 | H |
I-200 | (CH2)2-O-CH2CH2CH3 | CH2CH2CH3 | H |
I-201 | (CH2)2-O-CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-202 | (CH2)2-O-CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-203 | (CH2)2-O-CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-204 | (CH2)2-O-CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-205 | (CH2)2-O-CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-206 | (CH2)2-O-CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-207 | (CH2)2-O-CH(CH3)2 | CH2CH2CH3 | H |
I-208 | (CH2)2-O-C(CH3)3 | CH2CH2CH3 | H |
I-209 | (CH2)2-O-CH2C(CH3)3 | CH2CH2CH3 | H |
I-210 | (CH2)2-O-CH(CH3)CH2C(CH3)3 | CH2CH2CH3 | H |
I-211 | (CH2)2-O-CH(CH2CH3)CH2C(CH3)3 | CH2CH2CH3 | H |
I-212 | (CH2)2-O-CH2CH(CH3)CH2CH(CH3)2 | CH2CH2CH3 | H |
I-213 | (CH2)2-O-CH2CH(CH2CH3)CH2CH2CH3 | CH2CH2CH3 | H |
I-214 | (CH2)2-O-CH2CH2CH(CH3)CH2CH(CH3)2 | CH2CH2CH3 | H |
I-215 | (CH2)2-O-CH2CH2CH(CH3)CH2C(CH3)3 | CH2CH2CH3 | H |
I-216 | (CH2)2-O-CH2CH2CH(CH3)CH2CH2CH(CH3)2 | CH2CH2CH3 | H |
I-217 | (CH2)2-O-CH2CH2CH(CH3)CH2CH2CH2CH(CH3)2 | CH2CH2CH3 | H |
I-218 | (CH2)3-O-CH3 | CH2CH2CH3 | H |
I-219 | (CH2)3-O-CH2CH3 | CH2CH2CH3 | H |
I-220 | (CH2)3-O-CH2CH2CH3 | CH2CH2CH3 | H |
I-221 | (CH2)3-O-CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-222 | (CH2)3-O-CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-223 | (CH2)3-O-CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-224 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-225 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
I-226 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2CH2CH3 | H |
编号 | R1 | R2 | R3 |
I-227 | (CH2)3-O-CH(CH3)2 | CH2CH2CH3 | H |
I-228 | (CH2)3-O-C(CH3)3 | CH2CH2CH3 | H |
I-229 | (CH2)3-O-CH2C(CH3)3 | CH2CH2CH3 | H |
I-230 | (CH2)3-O-CH(CH3)CH2C(CH3)3 | CH2CH2CH3 | H |
I-231 | (CH2)3-O-CH(CH2CH3)CH2C(CH3)3 | CH2CH2CH3 | H |
I-232 | (CH2)3-O-CH2CH(CH3)CH2CH(CH3)2 | CH2CH2CH3 | H |
I-233 | (CH2)3-O-CH2CH(CH2CH3)CH2CH2CH3 | CH2CH2CH3 | H |
I-234 | (CH2)3-O-CH2CH2CH(CH3)CH2CH(CH3)2 | CH2CH2CH3 | H |
I-235 | (CH2)3-O-CH2CH2CH(CH3)CH2C(CH3)3 | CH2CH2CH3 | H |
I-236 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH(CH3)2 | CH2CH2CH3 | H |
I-237 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH2CH(CH3)2 | CH2CH2CH3 | H |
I-238 | CH2CH2CH3 | CH2OCH3 | H |
I-239 | CH2CH2CH2CH3 | CH2OCH3 | H |
I-240 | CH2CH2CH2CH2CH3 | CH2OCH3 | H |
1-241 | CH2CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-242 | CH2CH(CH3)CH2CH2CH3 | CH2OCH3 | H |
I-243 | CH2CH(CH2CH3)2 | CH2OCH3 | H |
I-244 | CH2CH2CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-245 | CH2CH2CH2CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-246 | CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-247 | CH2CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-248 | CH2CH2CH(CH3)CH2CH(CH3)3 | CH2OCH3 | H |
I-249 | (CH2)3-O-CH3 | CH2OCH3 | H |
I-250 | (CH2)3-O-CH2CH3 | CH2OCH3 | H |
1-251 | (CH2)3-O-CH2CH2CH3 | CH2OCH3 | H |
I-252 | (CH2)3-O-CH2CH2CH2CH3 | CH2OCH3 | H |
I-253 | (CH2)3-O-CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-254 | (CH2)3-O-CH2CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-255 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-256 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-257 | (CH2)3-O-CH2CH2CH2CH2CH2CH2CH2CH2CH3 | CH2OCH3 | H |
I-258 | (CH2)3-O-CH(CH3)2 | CH2OCH3 | H |
I-259 | (CH2)3-O-C(CH3)3 | CH2OCH3 | H |
I-260 | (CH2)3-O-CH2C(CH3)3 | CH2OCH3 | H |
1-261 | (CH2)3-O-CH(CH3)CH2C(CH3)3 | CH2OCH3 | H |
I-262 | (CH2)3-O-CH(CH2CH3)CH2C(CH3)3 | CH2OCH3 | H |
编号 | R1 | R2 | R3 |
I-263 | (CH2)3-O-CH2CH(CH3)CH2CH(CH3)2 | CH2OCH3 | H |
I-264 | (CH2)3-O-CH2CH(CH2CH3)CH2CH2CH3 | CH2OCH3 | H |
I-265 | (CH2)3-O-CH2CH2CH(CH3)CH2CH(CH3)2 | CH2OCH3 | H |
I-266 | (CH2)3-O-CH2CH2CH(CH3)CH2C(CH3)3 | CH2OCH3 | H |
I-267 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH(CH3)2 | CH2OCH3 | H |
I-268 | (CH2)3-O-CH2CH2CH(CH3)CH2CH2CH2CH(CH3)2 | CH2OCH3 | H |
I-269 | CH3 | (CH2)3CH3 | H |
I-270 | CH2CH3 | (CH2)3CH3 | H |
I-271 | CH2CH2CH3 | (CH2)3CH3 | H |
I-272 | CH2CH2CH2CH3 | (CH2)3CH3 | H |
I-273 | CH2CH2CH2CH2CH3 | (CH2)3CH3 | H |
I-274 | CH3 | (CH2)4CH3 | H |
I-275 | CH2CH3 | (CH2)4CH3 | H |
I-276 | CH2CH2CH3 | (CH2)4CH3 | H |
I-277 | CH2CH2CH2CH3 | (CH2)4CH3 | H |
I-278 | CH2CH2CH2CH2CH3 | (CH2)4CH3 | H |
I-279 | CH3 | (CH2)5CH3 | H |
1-280 | CH2CH3 | (CH2)5CH3 | H |
I-281 | CH2CH2CH3 | (CH2)5CH3 | H |
I-282 | CH2CH2CH2CH3 | (CH2)5CH3 | H |
I-283 | CH2CH2CH2CH2CH3 | (CH2)5CH3 | H |
I-284 | CH3 | (CH2)6CH3 | H |
I-285 | CH2CH3 | (CH2)6CH3 | H |
I-286 | CH2CH2CH3 | (CH2)6CH3 | H |
I-287 | CH2CH2CH2CH3 | (CH2)6CH3 | H |
I-288 | CH2CH2CH2CH2CH3 | (CH2)6CH3 | H |
I-289 | CH3 | (CH2)7CH3 | H |
I-290 | CH2CH3 | (CH2)7CH3 | H |
I-291 | CH2CH2CH3 | (CH2)7CH3 | H |
I-292 | CH2CH2CH2CH3 | (CH2)7CH3 | H |
I-293 | CH2CH2CH2CH2CH3 | (CH2)7CH3 | H |
I-294 | CH3 | (CH2)8CH3 | H |
I-295 | CH2CH3 | (CH2)8CH3 | H |
I-296 | CH2CH2CH3 | (CH2)8CH3 | H |
I-297 | CH2CH2CH2CH3 | (CH2)8CH3 | H |
I-298 | CH2CH2CH2CH2CH3 | (CH2)8CH3 | H |
本发明混合物的优选实施方案包含选自下列的化合物作为式I的活性化合物:
6-(3,4-二氯苯基)-5-甲基-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;
6-(4-叔丁基苯基)-5-甲基-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;
5-甲基-6-(3,5,5-三甲基己基)-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;
5-甲基-6-辛基-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;
5-乙基-6-辛基-[1,2,4]三唑并[1,5-a]嘧啶-2,7-二胺;
6-乙基-5-辛基-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;
5-乙基-6-辛基-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;
5-乙基-6-(3,5,5-三甲基己基)-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;
6-辛基-5-丙基-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;
5-甲氧基甲基-6-辛基-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;
6-辛基-5-三氟甲基-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺;和
5-三氟甲基-6-(3,5,5-三甲基己基)-[1,2,4]三唑并[1,5-a]嘧啶-7-基胺。
本发明的一个优选实施方案涉及至少一种式I化合物,尤其是上述优选化合物列中之一与至少一种选自如开头所定义的氨基甲酸酯类组的化合物II的混合物。氨基甲酸酯类优选选自虫螨威、丁硫克百威和硫双威。
本发明的另一优选实施方案涉及至少一种式I化合物,尤其是上列化合物之一与至少一种选自如开头所定义的合成除虫菊酯类组的化合物II的混合物。合成除虫菊酯类优选选自氟氯菊酯、氟氯氰菊酯、氯氰菊酯、甲体氯氰菊酯和七氟菊酯。
本发明的另一优选实施方案涉及至少一种式I化合物,尤其是上列化合物之一与至少一种选自如开头所定义的烟碱受体激动剂/拮抗剂化合物组的化合物II的混合物。烟碱受体激动剂/拮抗剂化合物优选选自吡虫清、噻虫胺、呋虫胺、吡虫啉、艾克敌105、噻虫嗪和噻虫啉。
本发明的另一优选实施方案涉及至少一种式I化合物,尤其是上列化合物之一与至少一种选自如开头所定义的GABA门控氯离子通道拮抗剂化合物组的化合物II的混合物。优选的GABA门控氯离子通道拮抗剂化合物为锐劲特。
优选实施方案为表A中所列的组合,其中在每种情况下表A中的一行对应于包含所述特定的式I化合物(组分a)和所述组中的一种活性化合物II(组分b)的农药组合,该活性化合物II优选选自上文定义的优选实施方案。
表A
编号 | 组分a | 组分b |
A-1 | 表1,I-9 | 选自组A.2的活性化合物II |
A-2 | 表1,I-9 | 选自组A.3的活性化合物II |
A-3 | 表1,I-9 | 选自组A.5的活性化合物II |
A-4 | 表1,I-9 | 选自组A.6的活性化合物II |
A-5 | 表1,I-18 | 选自组A.2的活性化合物II |
A-6 | 表1,I-18 | 选自组A.3的活性化合物II |
A-7 | 表1,I-18 | 选自组A.5的活性化合物II |
A-8 | 表1,I-18 | 选自组A.6的活性化合物II |
A-9 | 表1,1-25 | 选自组A.2的活性化合物II |
A-10 | 表1,I-25 | 选自组A.3的活性化合物II |
A-11 | 表1,I-25 | 选自组A.5的活性化合物II |
A-12 | 表1,I-25 | 选自组A.6的活性化合物II |
A-13 | 表1,I-28 | 选自组A.2的活性化合物II |
A-14 | 表1,I-28 | 选自组A.3的活性化合物II |
A-15 | 表1,I-28 | 选自组A.5的活性化合物II |
A-16 | 表1,I-28 | 选自组A.6的活性化合物II |
A-17 | 表1,I-98 | 选自组A.2的活性化合物II |
A-18 | 表1,I-98 | 选自组A.3的活性化合物II |
A-19 | 表1,I-98 | 选自组A.5的活性化合物II |
A-20 | 表1,I-98 | 选自组A.6的活性化合物II |
A-21 | 表1,I-101 | 选自组A.2的活性化合物II |
A-22 | 表1,I-101 | 选自组A.3的活性化合物II |
A-23 | 表1,I-101 | 选自组A.5的活性化合物II |
A-24 | 表1,I-101 | 选自组A.6的活性化合物II |
A-25 | 表1,I-110 | 选自组A.2的活性化合物II |
A-26 | 表1,I-110 | 选自组A.3的活性化合物II |
A-27 | 表1,I-110 | 选自组A.5的活性化合物II |
A-28 | 表1,I-110 | 选自组A.6的活性化合物II |
A-29 | 表1,I-113 | 选自组A.2的活性化合物II |
A-30 | 表1,I-113 | 选自组A.3的活性化合物II |
编号 | 组分a | 组分b |
A-31 | 表1,I-113 | 选自组A.5的活性化合物II |
A-32 | 表1,I-113 | 选自组A.6的活性化合物II |
A-33 | 表1,I-120 | 选自组A.2的活性化合物II |
A-34 | 表1,I-120 | 选自组A.3的活性化合物II |
A-35 | 表1,I-120 | 选自组A.5的活性化合物II |
A-36 | 表1,I-120 | 选自组A.6的活性化合物II |
A-37 | 表1,I-180 | 选自组A.2的活性化合物II |
A-38 | 表1,I-180 | 选自组A.3的活性化合物II |
A-39 | 表1,I-180 | 选自组A.5的活性化合物II |
A-40 | 表1,I-180 | 选自组A.6的活性化合物II |
A-41 | 表1,I-245 | 选自组A.2的活性化合物II |
A-42 | 表1,I-245 | 选自组A.3的活性化合物II |
A-43 | 表1,I-245 | 选自组A.5的活性化合物II |
A-44 | 表1,I-245 | 选自组A.6的活性化合物II |
A-45 | 表1,I-290 | 选自组A.2的活性化合物II |
A-46 | 表1,I-290 | 选自组A.3的活性化合物II |
A-47 | 表1,I-290 | 选自组A.5的活性化合物II |
A-48 | 表1,I-290 | 选自组A.6的活性化合物II |
式I化合物和化合物II能够与无机酸或有机酸或与金属离子形成盐或加合物。
无机酸的实例为氢卤酸,如氟化氢、氯化氢、溴化氢和碘化氢;硫酸、磷酸和硝酸。
合适的有机酸例如为甲酸、碳酸和链烷酸如乙酸、三氟乙酸、三氯乙酸和丙酸,以及乙醇酸、乳酸、丁二酸、柠檬酸、苯甲酸、肉桂酸、草酸、对甲苯磺酸、水杨酸、对氨基水杨酸、2-苯氧基苯甲酸或2-乙酰氧基苯甲酸。
合适的金属离子尤其是以下元素的离子:第一至第八过渡族元素,尤其是铬、锰、铁、钴、镍、铜、锌;以及另外的第二主族元素,尤其是钙和镁;和第三和第四主族元素,尤其是铝、锡和铅。合适的话,金属可以其可呈现的不同化合价存在。
上述活性化合物也可以其农业相容性盐的形式使用。这些盐通常为碱金属或碱土金属盐,如钠盐、钾盐或钙盐。
式I化合物也可以生物活性可能不同的各种晶型存在。它们也构成本发明主题的一部分。
在本发明的优选实施方案中,使用式I的唑并嘧啶基胺与活性化合物II的混合物。在某些条件下,可能有利的是将唑并嘧啶基胺与两种或更多种活性化合物II组合。另外,两种或更多种化合物I与一种或多种活性化合物II的混合物也可以是合适的。
当制备混合物时,优选使用纯活性化合物,需要的话,可将这些纯活性化合物与其它对抗有害真菌或其它害虫,如昆虫、蜘蛛或线虫的活性化合物或者作为另外活性组分的具除草活性或生长调节活性的化合物或肥料混合。
优选的其它杀虫剂为在开头作为组分b所述的那些,更优选上述优选化合物II。
优选的其他杀真菌剂为选自下列的那些:
·嗜球果伞素类(Strobilurins),如腈嘧菌酯(azoxystrobin)、醚菌胺(dimoxystrobin)、烯肟菌酯(enestroburin)、氟嘧菌酯(fluoxastrobin)、亚胺菌(kresoxim-methyl)、叉氨苯酰胺(metominostrobin)、肟醚菌胺(orysastrobin)、啶氧菌酯(picoxystrobin)、唑菌胺酯(pyraclostrobin)、pyribencarb、肟菌酯(trifloxystrobin)、2-(邻-((2,5-二甲基苯氧基亚甲基)苯基)-3-甲氧基丙烯酸甲酯;
·羧酰胺类,如N-酰苯胺类:苯霜灵(benalaxyl)、高苯霜灵(benalaxyl-M)、麦锈灵(benodanil)、bixafen、啶酰菌胺(boscalid)、萎锈灵(carboxin)、氯环丙酰胺(carpropamid)、双氯氰菌胺(diclocymet)、呋菌胺(fenfuram)、环酰菌胺(fenhexamide)、氟酰胺(flutolanil)、呋吡唑灵(furametpyr)、异噻菌胺(isotianil)、kiralaxyl、双炔酰菌胺(mandipropamid)、丙氧灭绣胺(mepronil)、甲霜灵(metalaxyl)、甲呋酰胺(ofurace)、噁霜灵(oxadixyl)、氧化萎锈灵(oxycarboxin)、吡噻菌胺(penthiopyrad)、硅噻菌胺(silthiofam)、溴氟唑菌(thifluzamide)、噻酰菌胺(tiadinil)、N-(3′,4′-二氯-5-氟-联苯-2-基)-3-二氟甲基-1-甲基-1H-吡唑-4-甲酰胺、N-(2-(1,3-二甲基-丁基)-苯基)-l,3-二甲基-5-氟-1H-吡唑-4-甲酰胺、N-(4′-氯-3′,5-二氟-联苯-2-基)-3-二氟甲基-1-甲基-1H-吡唑-4-甲酰胺、N-(4′-氯-3′,5-二氟-联苯-2-基)-3-三氟甲基-1-甲基-1H-吡唑-4-甲酰胺、N-(3′,4′-二氯-5-氟-联苯-2-基)-3-三氟甲基-1-甲基-1H-吡唑-4-甲酰胺、N-(3′,5-二氟-4′-甲基-联苯-2-基)-3-二氟甲基-1-甲基-1H-吡唑-4-甲酰胺、N-(3′,5-二氟-4′-甲基-联苯-2-基)-3-三氟甲基-1-甲基-1H-吡唑-4-甲酰胺、N-(2-双环丙基-2-基-苯基)-3-二氟甲基-1-甲基-1H-吡唑-4-甲酰胺、N-(顺-2-双环丙基-2-基-苯基)-3-二氟甲基-1-甲基-1H-吡唑-4-甲酰胺、N-(反-2-双环丙基-2-基-苯基)-3-二氟甲基-1-甲基-1H-吡唑-4-甲酰胺;
羧酸吗啉化物:烯酰吗啉(dimethomorph)、氟吗啉(flumorph);
苯甲酰胺类:氟联苯菌(flumetover)、氟吡菌胺(fluopicolide)、氟吡菌酰胺(fluopyram)、苯酰菌胺(zoxamide);
·唑类,如三唑类:戊环菌(azaconazole)、双苯三唑醇(bitertanol)、糠菌唑(bromuconazole)、环唑醇(cyproconazole)、噁醚唑(difenoconazole)、烯唑醇(diniconazole)、氧唑菌(epoxiconazole)、腈苯唑(fenbuconazole)、喹唑菌酮(fluquinconazole)、氟硅唑(flusilazole)、粉唑醇(flutriafol)、己唑醇(hexaconazole)、酰胺唑(imibenconazole)、环戊唑醇(ipconazole)、环戊唑菌(metconazole)、腈菌唑(myclobutanil)、oxpoconazol、多效唑(Paclobutrazol)、戊菌唑(penconazole)、丙环唑(propiconazole)、丙硫菌唑(prothioconazole)、硅氟唑(simeconazole)、戊唑醇(tebuconazole)、氟醚唑(tetraconazole)、三唑酮(triadimefon)、唑菌醇(triadimenol)、戊叉唑菌(triticonazole);
咪唑类:氰霜唑(cyazofamid)、烯菌灵(imazalil)、稻瘟酯(pefurazoate)、丙氯灵(prochloraz)、氟菌唑(triflumizole);
苯并咪唑类:苯菌灵(benomyl)、多菌灵(carbendazim)、麦穗宁(fuberidazole)、涕必灵(thiabendazole);
其他:噻唑菌胺(ethaboxam)、氯唑灵(etridiazole)、土菌消(hymexazole)、1-(4-氯-苯基)-1-(丙炔-2-基氧基)-3-(4-(3,4-二甲氧基-苯基)-异噁唑-5-基)-丙-2-酮;
·含氮杂环,如吡啶类:氟啶胺(fluazinam)、啶斑肟(pyrifenox)、3-[5-(4-氯苯基)-2,3-二甲基异噁唑烷-3-基]吡啶;
嘧啶类:磺嘧菌灵(bupirimate)、环丙嘧啶(cyprodinil)、氟嘧菌胺(diflumetorim)、异嘧菌醇(fenarimol)、嘧菌腙(ferimzone)、嘧菌胺(mepanipyrim)、氯定(nitrapyrin)、氟苯嘧啶醇(nuarimol)、二甲嘧菌胺(pyrimethanil);
吡咯类:拌种咯(fenpiclonil)、氟噁菌(fludioxonil);
吗啉类:4-十二烷基-2,6-二甲基吗啉(aldimorph)、吗菌灵(dodemorph)、丁苯吗啉(fenpropimorph)、克啉菌(tridemorph);
二羧酰亚胺类:唑啶草(fluoroimide)、异丙定(iprodione)、杀菌利(procymidone)、烯菌酮(vinclozolin);
非芳族5员环:噁唑酮菌(famoxadone)、咪唑菌酮(fenamidone)、异噻菌酮(octhilinone)、噻菌灵(probenazole);
其他:噻二唑素(acibenzolar-S-methyl)、吲唑磺菌胺(amisulbrom)、敌菌灵(anilazin)、灭瘟素(blasticidin-S)、敌菌丹(captafol)、克菌丹(captan)、灭螨猛(chinomethionat)、棉隆(dazomet)、双乙氧咪唑威(debacarb)、哒菌清(diclomezine)、氰菌胺(fenoxanil)、苯锈啶(fenpropidin)、灭菌丹(folpet)、粉病灵(piperalin)、丙氧喹啉(proquinazid)、咯喹酮(pyroquilon)、喹氧灵(quinoxyfen)、唑菌嗪(triazoxid)、三环唑(tricyclazole)、嗪氨灵(triforine)、5-氯-7-(4-甲基哌啶-1-基)-6-(2,4,6-三氟苯基)-[1,2,4]三唑并[1,5-a]嘧啶、2-丁氧基-6-碘-3-丙基苯并吡喃-4-酮;
·氨基甲酸盐和二硫代氨基甲酸盐,如二硫代氨基甲酸盐:福美铁(ferbam)、代森锰锌(mancozeb)、代森锰(maneb)、威百亩(metam)、代森联(metiram)、甲基代森锌(propineb)、福美双(thiram)、代森锌(zineb)、福美锌(ziram);
·氨基甲酸盐类:乙霉威(diethofencarb)、flubenthiavalicarb、异丙菌胺(iprovalicarb)、百维灵(propamocarb)、valiphenal、N-(1-(1-(4-氰基苯基)乙基磺酰基)丁-2-基)氨基甲酸4-氟苯基酯;
·胍类,如多果定(dodine)、双胍盐(guazatine)、双胍辛醋酸盐(iminoctadine);
抗菌素类:春雷素(kasugamycin)、多氧霉素(polyoxine)、链霉素(streptomycin)、井冈霉素(validamycin A);
·有机金属化合物类:三苯锡基盐(如薯瘟锡(fentin acetate)、三苯锡氯、毒菌锡(fentin hydroxide));
·含硫的杂环如:二噻农(dithianon)、稻瘟灵(isoprothiolane);
·有机磷化合物如:克瘟散(edifenphos)、藻菌磷(fosetyl)、乙膦铝(fosetyl-aluminum)、异稻瘟净(iprobenfos)、定菌磷(pyrazophos)、甲基立枯磷(tolclofos-methyl);
·有机氯化合物如:百菌清(chlorothalonil)、抑菌灵(dichlofluanid)、双氯酚(dichlorophen)、磺菌胺(flusulfamide)、六氯苯(hexachlorobenzene)、戊菌隆(pencycuron)、四氯苯酞(phthalide)、五氯硝基苯(quintozene)、甲基托布津(thiophanate-methyl)、对甲抑菌灵(tolylfluanid);
·无机活性化合物如:硫、亚磷酸(H3PO3)及其盐、铜盐如波尔多液(Bordeaux mixture)、醋酸铜、氢氧化铜、王铜(copper oxychloride)、碱式硫酸铜;
·硝基苯基衍生物:乐杀螨(binapacryl)、氯硝胺(dicloran)、敌螨通(dinobuton)、敌螨普(dinocap)、四氯硝基苯(tecnazen);
生长阻滞剂:调环酸(prohexadione)及其盐、抗倒酯(trinexapac-ethyl)、矮壮素阳离子(chlormequat)、甲哌鎓(mepiquat chloride)和二氟吡隆(diflufenzopyr);
·其他:溴硝丙二醇(bronopol)、环氟菌胺(cyflufenamid)、清菌脲(cymoxanil)、二苯胺(diphenylamine)、苯菌酮(metrafenone)、米多霉素(mildiomycin)、螺噁茂胺(spiroxamine)、对甲抑菌灵(tolylfluanid)、N-(环丙基甲氧基亚氨基-(6-二氟甲氧基-2,3-二氟苯基)-甲基)-2-苯基乙酰胺。
更优选其它杀真菌剂为选自下列的那些:
·唑类:苯菌灵、噁醚唑、氧唑菌、喹唑菌酮、粉唑醇、土菌消、烯菌灵、环戊唑菌、丙硫菌唑、戊唑醇;涕必灵、唑菌醇、丙氯灵、戊叉唑菌、多菌灵;
·嗜球果伞素类,如腈嘧菌酯、亚胺菌、肟醚菌胺、唑菌胺酯、肟菌酯;
·羧酰胺类,如啶酰菌胺、萎锈灵、甲霜灵、噁霜灵、烯酰吗啉、硅噻菌胺、双炔酰菌胺;
·杂环化合物如氟噁菌;克菌丹、棉隆、二甲嘧菌胺;异丙定;
·氨基甲酸盐类如代森锰锌、代森锰、代森联、福美双;
·其它活性化合物,其选自无机活性化合物:硫、波尔多液、醋酸铜、氢氧化铜、王铜、碱式硫酸铜;其它:双胍盐、链霉素。
其他优选实施方案为表B中所列的组合,其中在每种情况下表B中的一行对应于包含所述式I的特定化合物(组分a)和特定化合物II(组分b)的农药组合。这些二元组合中的每一个可另外含有一种或多种,尤其是一种上述其它杀虫剂或杀真菌剂。
编号 | 组分a | 组分b |
B-1 | 表1,I-9 | 虫螨威 |
B-2 | 表1,I-9 | 丁硫克百威 |
B-3 | 表1,I-9 | 硫双威 |
B-4 | 表1,I-9 | 氟氯菊酯 |
B-5 | 表1,I-9 | 氟氯氰菊酯 |
B-6 | 表1,I-9 | 氯氰菊酯 |
B-7 | 表1,I-9 | 甲体氯氰菊酯 |
B-8 | 表1,I-9 | 七氟菊酯 |
B-9 | 表1,I-9 | 吡虫清 |
B-10 | 表1,I-9 | 噻虫胺 |
B-11 | 表1,I-9 | 呋虫胺 |
B-12 | 表1,I-9 | 吡虫啉 |
B-13 | 表1,I-9 | 艾克敌105 |
B-14 | 表1,I-9 | 噻虫嗪 |
B-15 | 表1,I-9 | 噻虫啉 |
B-16 | 表1,I-9 | 锐劲特 |
B-17 | 表1,I-18 | 虫螨威 |
B-18 | 表1,I-18 | 丁硫克百威 |
B-19 | 表1,I-18 | 硫双威 |
B-20 | 表1,I-18 | 氟氯菊酯 |
B-21 | 表1,I-18 | 氟氯氰菊酯 |
B-22 | 表1,I-18 | 氯氰菊酯 |
B-23 | 表1,I-18 | 甲体氯氰菊酯 |
B-24 | 表1,I-18 | 七氟菊酯 |
编号 | 组分a | 组分b |
B-25 | 表1,I-18 | 吡虫清 |
B-26 | 表1,I-18 | 噻虫胺 |
B-27 | 表1,I-18 | 呋虫胺 |
B-28 | 表1,I-18 | 吡虫啉 |
B-29 | 表1,I-18 | 艾克敌105 |
B-30 | 表1,I-18 | 噻虫嗪 |
B-31 | 表1,I-18 | 噻虫啉 |
B-32 | 表1,I-18 | 锐劲特 |
B-33 | 表1,I-25 | 虫螨威 |
B-34 | 表1,I-25 | 丁硫克百威 |
B-35 | 表1,I-25 | 硫双威 |
B-36 | 表1,I-25 | 氟氯菊酯 |
B-37 | 表1,I-25 | 氟氯氰菊酯 |
B-38 | 表1,I-25 | 氯氰菊酯 |
B-39 | 表1,I-25 | 甲体氯氰菊酯 |
B-40 | 表1,I-25 | 七氟菊酯 |
B-41 | 表1,I-25 | 吡虫清 |
B-42 | 表1,I-25 | 噻虫胺 |
B-43 | 表1,I-25 | 呋虫胺 |
B-44 | 表1,I-25 | 吡虫啉 |
B-45 | 表1,I-25 | 艾克敌105 |
B-46 | 表1,I-25 | 噻虫嗪 |
B-47 | 表1,I-25 | 噻虫啉 |
B-48 | 表1,I-25 | 锐劲特 |
编号 | 组分a | 组分b |
B-49 | 表1,I-28 | 虫螨威 |
B-50 | 表1,I-28 | 丁硫克百威 |
B-51 | 表1,I-28 | 硫双威 |
B-52 | 表1,I-28 | 氟氯菊酯 |
B-53 | 表1,I-28 | 氟氯氰菊酯 |
B-54 | 表1,I-28 | 氯氰菊酯 |
B-55 | 表1,I-28 | 甲体氯氰菊酯 |
B-56 | 表1,I-28 | 七氟菊酯 |
B-57 | 表1,I-28 | 吡虫清 |
B-58 | 表1,I-28 | 噻虫胺 |
B-59 | 表1,I-28 | 呋虫胺 |
B-60 | 表1,I-28 | 吡虫啉 |
B-61 | 表1,I-28 | 艾克敌105 |
B-62 | 表1,I-28 | 噻虫嗪 |
B-63 | 表1,I-28 | 噻虫啉 |
B-64 | 表1,I-28 | 锐劲特 |
B-65 | 表1,I-98 | 虫螨威 |
B-66 | 表1,I-98 | 丁硫克百威 |
B-67 | 表1,I-98 | 硫双威 |
B-68 | 表1,I-98 | 氟氯菊酯 |
B-69 | 表1,I-98 | 氟氯氰菊酯 |
B-70 | 表1,I-98 | 氯氰菊酯 |
B-71 | 表1,I-98 | 甲体氯氰菊酯 |
B-72 | 表1,I-98 | 七氟菊酯 |
B-73 | 表1,I-98 | 吡虫清 |
B-74 | 表1,I-98 | 噻虫胺 |
B-75 | 表1,I-98 | 呋虫胺 |
B-76 | 表1,I-98 | 吡虫啉 |
B-77 | 表1,I-98 | 艾克敌105 |
B-78 | 表1,I-98 | 噻虫嗪 |
B-79 | 表1,I-98 | 噻虫啉 |
B-80 | 表1,I-98 | 锐劲特 |
B-81 | 表1,I-101 | 虫螨威 |
B-82 | 表1,I-101 | 丁硫克百威 |
B-83 | 表1,I-101 | 硫双威 |
B-84 | 表1,I-101 | 氟氯菊酯 |
编号 | 组分a | 组分b |
B-85 | 表1,I-101 | 氟氯氰菊酯 |
B-86 | 表1,I-101 | 氯氰菊酯 |
B-87 | 表1,I-101 | 甲体氯氰菊酯 |
B-88 | 表1,I-101 | 七氟菊酯 |
B-89 | 表1,I-101 | 吡虫清 |
B-90 | 表1,I-101 | 噻虫胺 |
B-91 | 表1,I-101 | 呋虫胺 |
B-92 | 表1,I-101 | 吡虫啉 |
B-93 | 表1,I-101 | 艾克敌105 |
B-94 | 表1,I-101 | 噻虫嗪 |
B-95 | 表1,I-101 | 噻虫啉 |
B-96 | 表1,I-101 | 锐劲特 |
B-97 | 表1,I-110 | 虫螨威 |
B-98 | 表1,I-110 | 丁硫克百威 |
B-99 | 表1,I-110 | 硫双威 |
B-100 | 表1,I-110 | 氟氯菊酯 |
B-101 | 表1,I-110 | 氟氯氰菊酯 |
B-102 | 表1,I-110 | 氯氰菊酯 |
B-103 | 表1,I-110 | 甲体氯氰菊酯 |
B-104 | 表1,I-110 | 七氟菊酯 |
B-105 | 表1,I-110 | 吡虫清 |
B-106 | 表1,I-110 | 噻虫胺 |
B-107 | 表1,I-110 | 呋虫胺 |
B-108 | 表1,I-110 | 吡虫啉 |
B-109 | 表1,I-110 | 艾克敌105 |
B-110 | 表1,I-110 | 噻虫嗪 |
B-111 | 表1,I-110 | 噻虫啉 |
B-112 | 表1,I-110 | 锐劲特 |
B-113 | 表1,I-113 | 虫螨威 |
B-114 | 表1,I-113 | 丁硫克百威 |
B-115 | 表1,I-113 | 硫双威 |
B-116 | 表1,I-113 | 氟氯菊酯 |
B-117 | 表1,I-113 | 氟氯氰菊酯 |
B-118 | 表1,I-113 | 氯氰菊酯 |
B-119 | 表1,I-113 | 甲体氯氰菊酯 |
B-120 | 表1,I-113 | 七氟菊酯 |
编号 | 组分a | 组分b |
B-121 | 表1,I-113 | 吡虫清 |
B-122 | 表1,I-113 | 噻虫胺 |
B-123 | 表1,I-113 | 呋虫胺 |
B-124 | 表1,I-113 | 吡虫啉 |
B-125 | 表1,I-113 | 艾克敌105 |
B-126 | 表1,I-113 | 噻虫嗪 |
B-127 | 表1,I-113 | 噻虫啉 |
B-128 | 表1,I-113 | 锐劲特 |
B-129 | 表1,I-120 | 虫螨威 |
B-130 | 表1,I-120 | 丁硫克百威 |
B-131 | 表1,I-120 | 硫双威 |
B-132 | 表1,I-120 | 氟氯菊酯 |
B-133 | 表1,I-120 | 氟氯氰菊酯 |
B-134 | 表1,I-120 | 氯氰菊酯 |
B-135 | 表1,I-120 | 甲体氯氰菊酯 |
B-136 | 表1,I-120 | 七氟菊酯 |
B-137 | 表1,I-120 | 吡虫清 |
B-138 | 表1,I-120 | 噻虫胺 |
B-139 | 表1,I-120 | 呋虫胺 |
B-140 | 表1,I-120 | 吡虫啉 |
B-141 | 表1,I-120 | 艾克敌105 |
B-142 | 表1,I-120 | 噻虫嗪 |
B-143 | 表1,I-120 | 噻虫啉 |
B-144 | 表1,I-120 | 锐劲特 |
B-145 | 表1,I-180 | 虫螨威 |
B-146 | 表1,I-180 | 丁硫克百威 |
B-147 | 表1,I-180 | 硫双威 |
B-148 | 表1,I-180 | 氟氯菊酯 |
B-149 | 表1,I-180 | 氟氯氰菊酯 |
B-150 | 表1,I-180 | 氯氰菊酯 |
B-151 | 表1,I-180 | 甲体氯氰菊酯 |
B-152 | 表1,I-180 | 七氟菊酯 |
B-153 | 表1,I-180 | 吡虫清 |
B-154 | 表1,I-180 | 噻虫胺 |
B-155 | 表1,I-180 | 呋虫胺 |
B-156 | 表1,I-180 | 吡虫啉 |
编号 | 组分a | 组分b |
B-157 | 表1,I-180 | 艾克敌105 |
B-158 | 表1,I-180 | 噻虫嗪 |
B-159 | 表1,I-180 | 噻虫啉 |
B-160 | 表1,I-180 | 锐劲特 |
B-161 | 表1,I-245 | 虫螨威 |
B-162 | 表1,I-245 | 丁硫克百威 |
B-163 | 表1,I-245 | 硫双威 |
B-164 | 表1,I-245 | 氟氯菊酯 |
B-165 | 表1,I-245 | 氟氯氰菊酯 |
B-166 | 表1,I-245 | 氯氰菊酯 |
B-167 | 表1,I-245 | 甲体氯氰菊酯 |
B-168 | 表1,I-245 | 七氟菊酯 |
B-169 | 表1,I-245 | 吡虫清 |
B-170 | 表1,I-245 | 噻虫胺 |
B-171 | 表1,I-245 | 呋虫胺 |
B-172 | 表1,I-245 | 吡虫啉 |
B-173 | 表1,I-245 | 艾克敌105 |
B-174 | 表1,I-245 | 噻虫嗪 |
B-175 | 表1,I-245 | 噻虫啉 |
B-176 | 表1,I-245 | 锐劲特 |
B-177 | 表1,I-290 | 虫螨威 |
B-178 | 表1,I-290 | 丁硫克百威 |
B-179 | 表1,I-290 | 硫双威 |
B-180 | 表1,I-290 | 氟氯菊酯 |
B-181 | 表1,I-290 | 氟氯氰菊酯 |
B-182 | 表1,I-290 | 氯氰菊酯 |
B-183 | 表1,I-290 | 甲体氯氰菊酯 |
B-184 | 表1,I-290 | 七氟菊酯 |
B-185 | 表1,I-290 | 吡虫清 |
B-186 | 表1,I-290 | 噻虫胺 |
B-187 | 表1,I-290 | 呋虫胺 |
B-188 | 表1,I-290 | 吡虫啉 |
B-189 | 表1,I-290 | 艾克敌105 |
B-190 | 表1,I-290 | 噻虫嗪 |
B-191 | 表1,I-290 | 噻虫啉 |
B-192 | 表1,I-290 | 锐劲特 |
在另一优选实施方案中,混合物仅包含两种活性成分。各优选实施方案与上述实施方案一致。
在另一优选实施方案中,混合物仅包含三种活性成分。更优选的是可另外含有另一种活性化合物,尤其是另一种杀真菌剂的组合B-1至B-192中的任一个。各优选实施方案与上述实施方案一致。
在一个实施方案中,本发明混合物用于对抗有害真菌和有害昆虫或线虫。
在另一实施方案中,本发明混合物用于对抗有害真菌。
式I化合物与化合物II的混合物尤其适用于防治以下有害真菌:卵菌纲(Peronosporomycetes)(同义词:Oomycetes),如霜霉(Peronospora)属、疫霉(Phytophthora)属、葡萄生单轴霉(Plasmopara viticola)和假霜霉属(Pseudoperonospora),尤其是对应于下述那些的真菌。
在另一实施方案中,本发明混合物用于对抗有害昆虫或线虫。
在另一实施方案中,本发明混合物包含协同增效有效量的式I化合物与化合物II。
在另一实施方案中,本发明混合物包含协同增效有效量的式I化合物与化合物II并用于对抗有害昆虫或线虫。
在另一实施方案中,本发明混合物用于防治真菌和/或改善植物健康的方法,该方法包括用至少一种式I化合物和至少一种化合物II以任何所需顺序或同时,即联合或分开处理受真菌侵染或易受真菌侵染的位置,例如植物或植物繁殖材料。
在另一实施方案中,本发明混合物用于防治有害昆虫或线虫的方法,该方法包括用至少一种式I化合物和至少一种化合物II以任何所需顺序或同时,即联合或分开处理受真菌侵染或易受真菌侵染的位置,例如植物或植物繁殖材料。
在另一实施方案中,本发明混合物用于一种改善植物健康的方法,该方法包括用至少一种式I化合物和至少一种化合物II以任何所需顺序或同时,即联合或分开处理受真菌侵染或易受真菌侵染的位置,例如植物或植物繁殖材料。
在该方法的另一实施方案中,至少一种式I化合物和至少一种化合物II的施用可在无害虫压力的情况下进行。
在另一实施方案中,本发明混合物包含协同增效有效量的式I化合物与化合物II并用于改善植物的健康。该方法可在害虫压力下或在无害虫压力的情况下应用。
在另一优选实施方案中,本发明混合物用于活的植物作物的叶面施用、用于播种或种植前的土壤施用(包括整个土壤处理和犁沟施用)以及尤其用于针对植物繁殖材料的拌种施用。植物繁殖材料涵盖所有种类的种子(果实、块茎、谷粒)、插枝、伐条等。一个特殊应用领域为所有种类种子的处理。
本发明混合物对于防治各种作物植物和这些植物的种子或牧草和牧草种子上的大量真菌和昆虫或线虫尤其重要,其中这些作物植物例如为小麦、玉米、黑麦、大麦、燕麦、高粱、稻、玉蜀黍、草、香蕉、棉花、大豆、咖啡、甘蔗、葡萄藤、水果种类、观赏植物和蔬菜,如黄瓜、菜豆、干豆、西红柿、马土豆、莴苣、葫芦、莴苣、胡萝卜、十字花科植物、向日葵和葫芦。在特定实施方案中,将本发明混合物施用于大豆上。在另一优选实施方案中,将本发明混合物施用于种子上。在特定实施方案中,将本发明混合物施用于大豆种子上。
化合物I可用作大量不同活性化合物II的增效剂。同时,即联合地或分开地施用至少一种式I化合物与活性化合物II以超加合方式增加杀真菌活性和/或增加植物健康的活性。
具体而言,式I化合物和混合物适用于防治以下有害真菌:
·蔬菜、油菜籽、糖用甜菜、禾谷类、水果和稻上的链格孢(Alternaria)属,例如土豆和西红柿上的早疫链格孢(A.solani)或细交链孢(A.alternata),
·糖用甜菜和蔬菜上的丝囊霉(Aphanomyces)属,
·禾谷类和蔬菜上的壳二孢(Ascochyta)属,例如小麦上的小麦裾叶炫菌(Ascochyta tritici)(叶斑病),
·玉米、禾谷类、稻和草坪中的平脐蠕孢(Bipolaris)属和内脐蠕孢(Drechslera)属,例如玉米上的玉米小斑病菌(D.maydis),
·禾谷类(例如小麦或大麦)中的禾白粉菌(Blumeria graminis)(白粉病),
·草莓、蔬菜、花卉、小麦和葡萄糖上的灰葡萄孢(Botrytis cinerea),
·莴苣上的莴苣盘梗霉(Bremia lactucae),
·玉米、大豆、稻和糖用甜菜上的尾孢(Cercospora)属,例如大豆上的大豆尾孢(Cercospora sojina)或菊池尾孢(Cercospora kikuchii),
·小麦上的扁豆枝孢(Cladosporium herbarum),
·玉米、禾谷类和稻上的旋孢腔菌(Cochliobolus)属,例如禾谷类上的禾旋孢腔菌(Cochliobolus sativus),和稻上的宫部旋孢腔菌(Cochliobolusmiyabeanus)),
·大豆和棉花上的剌盘孢(Colletotricum)属,例如大豆上的毛豆炭疽病菌(Colletotrichum truncatum),
·大豆上的山扁豆生棒孢(Corynespora cassiicola),
·大豆上的白纹羽束丝菌(Dematophora necatrix),
·大豆上的菜豆间座壳(Diaporthe phaseolorum),
·玉米、禾谷类、稻和草坪上的内脐蠕孢(Drechslera)属、核腔菌(Pyrenophora)属,例如大麦网斑内脐蠕孢(D.teres))或小麦上的D.tritci-repentis),
·由Phaeoacremonium chlamydosporium、Ph.Aieophilum和Formitipora punctata(同义词斑孔木层孔菌(Phellinus punctatus))引起的葡萄藤上的埃斯卡(Esca);
·葡萄藤上的痂囊腔菌(Elsinoe ampelina),
·稻上的Entyloma oryzae,
·小麦上的附球菌属(Epicoccum),
·玉米上的突脐蠕孢(Exserohilum)属,
·黄瓜上的二孢白粉菌(Erysiphe cichoracearum)和单丝壳白粉菌(Sphaerotheca fuliginea),
·各种植物上的镰孢霉(Fusarium)属和轮枝孢(Verticillium)属,例如禾谷类上的禾谷镰刀菌(F.graminearum)或大刀镰孢(F.culmorum)或多种植物,如西红柿上的尖镰孢(F.oxysporum),和大豆上的真马特腐皮镰孢(Fusarium Solani)
·禾谷类,如大麦或小麦上的禾顶囊壳(Gaeumanomyces graminis)属,
·葡萄藤和其它作物上的围小丛壳(Glomerella cingulata),
·禾谷类和稻上的赤霉(Gibberella)属,例如稻上的藤仓赤霉(Gibberella fujikuroi),
·稻上的革兰氏染色配合物(Grainstaining complex),
·葡萄藤上的葡萄球座菌(Guignardia budwelli),
·玉米和稻上的长蠕孢(Helminthosporium)属,
·葡萄藤上的褐斑拟棒束孢(Isariopsis clavispora),
·大豆上的菜豆格孢(Macrophomina phaseolina),
·禾谷类上的Michrodochium nivale,
·大豆上的Microsphaera diffusa,
·禾谷类、香蕉和花生上的球腔菌(Mycosphaerella)属,例如小麦上的禾生球腔菌(M.graminicola)或香蕉上的M.fijiesis,
·甘蓝和洋葱植物上的霜霉(Peronospora)属,例如甘蓝上的芸苔霜霉(P.brassicae),洋葱上的P.destructor,或大豆上的东北霜霉(Peronosporamanshurica),
·大豆上的豆薯层锈菌(Phakopsora pachyrhizi)和山马蟥层锈菌(Phakopsara meibomiae),
·大豆上的Phialophora gregata,
·向日葵、葡萄藤和大豆上的拟茎点霉(Phomopsis)属(大豆上的P.phaseoli和葡萄藤上的葡萄拟茎点霉(P.viticola)),
·各种植物上的疫霉属(Phytophthora),例如胡椒上的辣椒疫霉(P.capsici),大豆上的大雄疫霉(P.megasperma),土豆和西红柿上的致病疫霉(P.infestans),
·葡萄藤上的葡萄生单轴霉(Plasmopara viticola),
·苹果上的苹果白粉病菌(Podosphaera leucotricha),
·禾谷类上(小麦或大麦)的小麦基腐病菌(Pseudocercosporellaherpotrichoides),
·各种植物上的假霜霉(Pseudoperonospora)属,例如黄瓜上的古巴假霜霉(P.cubenis)或啤酒花上的葎草假霜霉(P.humili),
·葡萄藤上的Pseudopezicula tracheiphilai,
·各种植物上的柄锈菌(Puccinia)属,例如禾谷类(大麦和小麦)上的小麦锈病菌(P.triticina),条锈病菌(P.striformis),大麦锈病菌(P.hordei)或禾柄锈菌(P.graminis)或芦笋上的芦笋锈病菌(P.asparagi),
·稻上的稻瘟病菌(Pyricularia oryzae)、笹木伏革菌(Corticiumsasaii)、帚梗柱孢属(Sarocladium oryzae)、稻叶鞘腐败病(S.attenuatum)、稻叶黑粉菌(Entyloma oryzae)
·小麦上的Pyrenophora tritici-repentis或大麦上的Pyrenophorateres
·草坪和禾谷类上的稻梨孢菌(Pyricularia grisea),
·草坪、稻、玉米、小麦、棉花、油菜籽、向日葵、糖用甜菜、蔬菜和其他植物上的腐霉(Pythium)属,例如各种植物上的终极腐霉(P.ultimum)、草坪上的瓜果腐霉(P.aphanidermatum)),
·大麦上的Ramularia collo-cygni(生理叶斑病),
·棉花、稻、土豆、草坪、玉米、油菜籽、土豆、糖用甜菜、蔬菜和各种植物上的丝核菌(Rhizoctonia)属,例如甜菜和各种植物上的立枯丝核病菌(Rhizoctonia solani),和小麦或大麦上的禾谷丝核菌(Rhizoctoniacerealis),
·大麦、黑麦和黑小麦上的黑麦喙孢(Rhynchosporium secalis),
·油菜籽、向日葵和大豆上的核盘菌(Sclerotinia)属,例如大豆上的核盘菌(Sclerotinia sclerotiorum)或Sclerotinia rolfsii,
·大豆上的大豆壳针孢(Septoria glycines),
·小麦上的小麦壳针孢(Septoria tritici)和颖枯壳多孢(Stagonosporanodorum),
·葡萄藤上的葡萄钩丝壳(Erysiphe(同义词Uncinula necator),
·玉米和草坪上的Setospaeria属,
·玉米上的丝轴黑粉菌(Sphacelotheca reilinia),
·小麦上的颖枯壳多孢(Stagonospora nodorum),
·大豆和棉花上的根串珠霉(Thievaliopsis)属,
·禾谷类上的腥黑粉菌(Tilletia)属,
·小麦或大麦上的肉孢核瑚菌(Typhula incarnate),
·禾谷类、玉米和甘蔗上的黑粉菌(Ustilago)属,例如玉米上的玉蜀黍黑粉菌(U.maydis),
·苹果和梨上的黑星菌(Venturia)属(黑星病),例如苹果上的苹果黑星病(V.inaequalis)。
它们还适用于防治选自如下目的有害昆虫:
·鳞翅目(Lepidoptera),例如小地老虎(Agrotis ypsilon)、黄地老虎(Agrotis segetum)、木棉虫(Alabama argillacea)、黎豆夜蛾(Anticarsiagemmatalis)、Argyresthia conjugella、叉纹夜蛾(Autographa gamma)、树尺蠖(Bupalus piniarius)、Cacoecia murinana、Capua reticulana、Cheimatobia brumata、云杉色卷蛾(Choristoneura fumiferana)、Choristoneura occidentalis、二化螟(Cirphis unipuncta)、苹果小卷蛾(Cydiapomonella)、松毛虫(Dendrolimus pini)、Diaphania nitidalis、西南玉米杆草螟(Diatraea grandiosella)、埃及钻夜蛾(Earias insulana)、南美玉米苗斑螟(Elasmopalpus lignosellus)、女贞细卷蛾(Eupoecilia ambiguella)、Evetriabouliana、Feltia subterranea、蜡螟(Galleria mellonella)、李小食心虫(Grapholitha funebrana)、梨小食心虫(Grapholitha molesta)、棉铃虫(Heliothis armigera)、烟芽夜蛾(Heliothis virescens)、玉米穗虫(Heliothiszea)、菜螟(Hellula undalis)、Hibernia defoliaria、美国白蛾(Hyphantriacunea)、苹果巢蛾(Hyponomeuta malinellus)、番茄虫蛾(Keiferialycopersicella)、Lambdina fiscellaria、甜菜夜蛾(Laphygma exigua)、咖啡潜叶蛾(Leucoptera coffeella)、旋纹潜蛾(Leucoptera scitella)、Lithocolletisblancardella、葡萄浆果小卷蛾(Lobesia botrana)、甜菜网螟(Loxostegesticticalis)、舞毒蛾(Lymantria dispar)、模毒蛾(Lymantria monacha)、桃潜蛾(Lyonetia clerkella)、黄褐天幕毛虫(Malacosoma neustria)、甘蓝夜蛾(Mamestra brassicae)、黄杉毒蛾(Orgyia pseudotsugata)、玉米螟(Ostrinianubilalis)、小眼夜蛾(Panolis flammea)、棉花红铃虫(Pectinophoragossypiella)、疆夜蛾(Peridroma saucia)、圆掌舟蛾(Phalera bucephala)、马铃薯麦蛾(Phthorimaea operculella)、柑桔潜叶蛾(Phyllocnistis citrella)、欧洲粉蝶(Pieris brassicae)、苜蓿绿夜蛾(Plathypena scabra)、菜蛾(Plutellaxylostella)、大豆夜蛾(Pseudoplusia includens)、Rhyacionia frustrana、Scrobipalpula absoluta、麦蛾(Sitotroga cerealella)、葡萄卷叶蛾(Sparganothis pilleriana)、草地夜蛾(Spodoptera frugiperda)、海灰翅夜蛾(Spodoptera littoralis)、斜纹夜蛾(Spodoptera litura)、Thaumatopoeapityocampa、绿色橡木飞蛾(Tortrix viridana)、粉纹夜蛾(Trichoplusia ni)和Zeiraphera canadensis,
·甲虫(鞘翅目(Coleoptera)),例如梨窄吉丁(Agrilus sinuatus)、直条叩头虫(Agriotes lineatus)、暗色叩头虫(Agriotes obscurus)、Amphimallussolstitialis、Anisandrus dispar、墨西哥棉铃象(Anthonomus grandis)、苹花象(Anthonomus pomorum)、甜菜隐食甲(Atomaria linearis)、纵坑切梢小蠹(Blastophagus piniperda)、Blitophaga undata、蚕豆象(Bruchusrufimanus)、豌豆象(Bruchus pisorum)、欧洲兵豆象(Bruchus lentis)、苹卷象(Byctiscus betulae)、甜菜大龟甲(Cassida nebulosa)、Cerotomatrifurcata、白菜籽龟象(Ceuthorrhynchus assimilis)、芫菁龟象(Ceuthorrhynchus napi)、甜菜胫跳甲(Chaetocnema tibialis)、Conoderusvespertinus、石刁柏负泥虫(Crioceris asparagi)、长角叶甲(Diabroticalongicornis)、Diabrotica 12-punctata、玉米根叶甲(Diabrotica virgifera)、墨西哥豆瓢虫(Epilachna varivestis)、烟草跳甲(Epitrix hirtipennis)、棉灰蒙象变种(Eutinobothrus brasiliensis)、欧洲松树皮象(Hylobius abietis)、埃及苜蓿叶象(Hypera brunneipennis)、紫苜蓿叶象(Hypera postica)、云杉八齿小蠹(Ips typographus)、烟草负泥虫(Lema bilineata)、黑角负泥虫(Lemamelanopus)、马铃薯叶甲(Leptinotarsa decemlineata)、Limoniuscalifornicus、稻水象甲(Lissorhoptrus oryzophilus)、Melanotus communis、油菜露尾甲(Meligethes aeneus)、大栗鳃金龟(Melolontha hippocastani)、五月鳃金龟(Melolontha melolontha)、水稻负泥虫(Oulema oryzae)、葡萄黑耳喙象(Ortiorrhynchus sulcatus)、草莓根象甲(Otiorrhynchus ovatus)、辣根猿叶甲(Phaedon cochleariae)、Phyllotreta chrysocephala、食叶鳃金龟属(Phyllophaga sp.)、庭园发丽金龟(Phyllopertha horticola)、大豆淡足跳甲(Phyllotreta nemorum)、黄曲条菜跳甲(Phyllotreta striolata)、日本金龟子(Popillia japonica)、豌豆叶象(Sitona lineatus)和谷象(Sitophilusgranaria),
·双翅目(Diptera),例如埃及伊蚊(Aedes aegyptii)、剌扰伊蚊(Aedesvexans)、墨西哥果蝇(Anastrepha ludens)、五斑按蚊(Anophelesmaculipennis)、地中海实蝇(Ceratitis capitata)、蛆症金蝇(Chrysomyabezziana)、Chrysomya hominivorax、Chrysomya macellaria、高粱瘿蚊(Contarinia sorghicola)、嗜人瘤蝇蛆(Cordylobia anthropophaga)、尖音库蚊(Culex pipiens)、瓜蝇(Dacus cucurbitae)、油橄榄实蝇(Dacus oleae)、油菜叶瘿蚊(Dasineura brassicae)、小毛厕蝇(Fannia canicularis)、马蝇(Gasterophilus intestinalis)、刺舌蝇(Glossina morsitans)、Haematobiairritans、Haplodiplosis equestris、花生田灰地种蝇(Hylemyia platura)、纹皮蝇(Hypoderma lineata)、蔬菜斑潜蝇(Liriomyza sativae)、美国潜叶蝇(Liriomyza trifolii)、Lucilia caprina、铜绿蝇(Lucilia cuprina)、丝光绿蝇(Lucilia sericata)、Lycoria pectoralis、麦瘿蚊(Mayetiola destructor)、家蝇(Musca domestica)、厩腐蝇(Muscina stabulans)、羊狂蝇(Oestrus ovis)、欧洲麦秆蝇(Oscinella frit)、天仙子泉蝇(Pegomya hysocyami)、葱蝇(Phorbia antiqua)、萝卜蝇(Phorbia brassicae)、麦地种蝇(Phorbiacoarctata)、樱桃实蝇(Rhagoletis cerasi)、苹果实蝇(Rhagoletispomonella)、牛虻(Tabanus bovinus)、Tipula oleracea和欧洲大蚊(Tipulapaludosa),
·蓟马(缨翅目(Thysanoptera)),例如烟褐蓟马(Frankliniella fusca)、苜蓿花蓟马(Frankliniella occidentalis)、东方花蓟马(Frankliniellatritici)、桔硬蓟马(Scirtothrips citri)、稻蓟马(Thrips oryzae)、棕榈蓟马(Thrips palmi)和烟蓟马(Thrips tabaci),
·膜翅目(Hymenoptera)),例如新疆菜叶蜂(Athalia rosae)、切叶蚁(Atta cephalotes)、Atta sexdens、Atta texana、Hoplocampa minuta、Hoplocampa testudinea、小黄家蚁(Monomorium pharaonis)、热带火蚁(Solenopsis geminate)和红火蚁(Solenopsis invicta),
·异翅目(Heteroptera),例如拟绿蝽(Acrosternum hilare)、玉米长蝽(Blissus leucopterus)、黑斑烟盲蝽(Cyrtopeltis notatus)、棉红蝽(Dysdercus cingulatus)、Dysdercus intermedius、麦扁盾蝽(Eurygasterintegriceps)、烟草蝽(Euschistus impictiventris)、棉红铃喙缘蝽(Leptoglossus phyllopus)、美洲牧草盲蝽(Lygus lineolaris)、牧草盲蝽(Lygus pratensis)、稻绿蝽(Nezara viridula)、甜菜拟网蝽(Piesmaquadrata)、Solubea insularis和Thyanta perditor、
·同翅目(Homoptera),如Acyrthosiphon onobrychis、落叶松球蚜(Adelges laricis)、Aphidula nasturtii、甜菜蚜(Aphis fabae)、草莓根蚜(Aphis forbesi)、苹果蚜(Aphis pomi)、棉蚜(Aphis gossypii)、北美茶簏子蚜(Aphis grossulariae)、希奈德蚜(Aphis schneideri)、卷叶蚜(Aphisspiraecola)、接骨木蚜(Aphis sambuci)、豌豆蚜(Acyrthosiphon pisum)、茄无网蚜(Aulacorthum solani)、飞廉短尾蚜(Brachycaudus cardui)、李短尾蚜(Brachycaudus helichrysi)、桃短尾蚜(Brachycaudus persicae)、Brachycaudus prunicola、甘蓝蚜(Brevicoryne brassicae)、Capitophorushorni、Cerosipha gossypii、草莓中瘤钉毛蚜(Chaetosiphon fragaefolii)、茶镳隐瘤蚜(Cryptomyzus ribis)、高加索冷杉椎球蚜(Dreyfusianordmannianae)、云杉椎球蚜(Dreyfusia piceae)、居根西圆尾蚜(Dysaphisradicola)、Dysaulacorthum pseudosolani、车前圆尾蚜(Dysaphisplantaginea)、梨西圆尾蚜(Dysaphis pyri)、蚕豆微叶蝉(Empoascafabae)、桃大尾蚜(Hyalopterus pruni)、Hyperomyzus lactucae、麦长管蚜(Macrosiphum avenae)、大戟长管蚜(Macrosiphum euphorbiae)、蔷薇管蚜(Macrosiphon rosae)、巢莱修尾蚜(Megoura viciae)、Melanaphispyrarius、麦无网蚜(Metopolophium dirhodum)、Myzodes persicae、冬葱瘤额蚜(Myzus ascalonicus)、Myzus cerasi、李瘤蚜(Myzus varians)、黑茶镳子衲长管蚜(Nasonovia ribis-nigri)、稻飞虱(Nilaparvata lugens)、囊柄瘿绵蚜(Pemphigus bursarius)、蔗飞虱(Perkinsiella saccharicida)、忽布疣蚜(Phorodon humuli)、苹木虱(Psylla mali)、梨木虱(Psylla piri)、冬葱瘤蛾蚜(Rhopalomyzus ascalonicus)、玉米蚜(Rhopalosiphum maidis)、禾谷溢管蚜(Rhopalosiphum padi)、苹草缢管蚜(Rhopalosiphum insertum)、Sappaphis mala、Sappaphis mali、麦二叉蚜(Schizaphis graminum)、Schizoneura lanuginosa、麦长管蚜(Sitobion avenae)、白粉虱(Trialeurodes vaporariorum)、桔二叉蚜(Toxoptera aurantiiand)和葡萄根瘤蚜(Viteus vitifolii)。
·白蚁(等翅目),例如Calotermes flavicollis、Leucotermes flavipes、欧洲散白蚁(Reticulitermes lucifugus)和Termes natalensis,
·直翅目(orthoptera),例如居屋艾蟋(Acheta domestica)、东方蜚蠊(Blatta orientalis)、德国小蠊(Blattella germanica)、欧洲球螋(Forficulaauricularia)、蝼蛄(Gryllotalpa gryllotalpa)、飞蝗(Locusta migratoria)、双纹黑蝗(Melanoplus bivittatus)、红足黑蝗(Melanoplus femur-rubrum)、墨西哥黑蝗(Melanoplus mexicanus)、迁飞黑蝗(Melanoplus sanguinipes)、石栖黑蝗(Melanoplus spretus)、条纹红蝗(Nomadacris septemfasciata)、美洲大蠊(Periplaneta americana)、美洲沙漠蝗(Schistocerca americana)、Schistocerca peregrina、Stauronotus maroccanus和庭疾灶螽(Tachycinesasynamorus),
·蜘蛛纲(Arachnoidea)),如蜘蛛(蜱螨目(Acarina)),例如软蜱科(Argasidae)、硬蜱科(Ixodidae)和疥螨科(Sarcoptidae),如长星形壁虱(Amblyomma americanum)、热带花蜱(Amblyomma variegatum)、波斯锐缘蜱(Argas persicus)、牛壁虱(Boophilus annulatus)、Boophilusdecoloratus、微小牛蜱(Boophilus microplus)、Dermacentor silvarum、Hyalomma truncatum、蓖子硬蜱(Ixodes ricinus)、Ixodes rubicundus、Ornithodorus moubata、Otobius megnini、鸡皮刺螨(Dermanyssusgallinae)、绵羊疥病(Psoroptes ovis)、Rhipicephalus appendiculatus、Rhipicephalus evertsi、人疥螨(Sarcoptes scabiei),瘿螨(Eriophyidae)属,如苹果刺锈螨(Aculus schlechtendali)、Phyllocoptrata oleivora和Eriophyes sheldoni;细螨(Tarsonemidae)属,如Phytonemus pallidus和侧多食跗线螨(Polyphagotarsonemus latus);细须螨(Tenuipalpidae)属,如紫红短须螨(Brevipalpus phoenicis);叶螨(Tetranychidae)属,如朱砂叶螨(Tetranychus cinnabarinus)、神泽叶螨(Tetranychus kanzawai)、太平洋叶螨(Tetranychus pacificus)、棉叶螨(Tetranychus telarius)和二点叶螨(Tetranychus urticae),苹果叶螨(Panonychus ulmi)、柑椐叶螨(Panonychus citri)和草地小爪螨(Oligonychus pratensis);
它们还适用于防治如下有害线虫,尤其是植物寄生线虫如根结线虫,北方根结线虫(Meloidogyne hapla)、南方根结线虫(Meloidogyneincognita)、爪哇根结线虫(Meloidogyne javanica)和其它根结线虫属(Meloidogyne);形成胞囊的线虫,马铃薯金线虫(Globodera rostochiensis)和其它球胞囊(Globodera)属;禾谷胞囊线虫(Heterodera avenae)、大豆胞囊线虫(Heterodera glycines)、甜菜胞囊线虫(Heterodera schachtii)、三叶草胞囊线虫(Heterodera trifolii)和其它胞囊线虫(Heterodera)属;种子肿瘿线虫,粒线虫(Anguina)属;茎叶线虫,滑刃线虫(Aphelenchoides)属;刺线虫,杂草刺线虫(Belonolaimus longicaudatus)和其它针刺线虫属(Belonolaimus);松线虫,松材线虫(Bursaphelenchus xylophilus)和其它伞滑刃线虫属(Bursaphelenchus);环形线虫,环纹线虫属(Criconema)、小环线虫属(Criconemella)、轮线虫属(Criconemoides)、中环线虫属(Mesocriconema);球茎线虫,腐烂茎线虫(Ditylenchus destructor)、甘薯茎线虫(Ditylenchus dipsaci)和其它茎线虫属(Ditylenchus);锥线虫,锥线虫属(Dolichodorus);螺旋形线虫,Heliocotylenchus multicinctus和其它Helicotylenchus属;鞘线虫和鞘形(sheathoid)线虫,鞘线虫属(Hemicycliophora)和Hemicriconemoides属;Hirshmanniella属;冠线虫,Hoploaimus属;伪根结线虫,珍珠线虫属(Nacobbus);针线虫,Longidoruselongatus和其它长针线虫属(Longidorus);根腐线虫,Pratylenchusncglectus、穿刺根腐线虫(Pratylenchus penetrans)、Pratylenchuscurvitatus、Pratylenchus goodeyi和其它根腐线虫属(Pratylenchus);穿孔线虫,香蕉穿孔线虫(Radopholus similis)和其它穿孔线虫属(Radopholus);肾形线虫,Rotylenchus robustus和其它盘旋线虫属(Rotylenchus);Scutellonema属;残根线虫,Trichodorus primitivus和其它毛刺线虫属(Trichodorus)、拟毛刺属(Paratrichodorus);阻长线虫,Tylenchorhynchusclaytoni、Tylenchorhynchus dubius 和其它矮化线虫属(Tylenchorhynchus);柑桔线虫,垫刃线虫属(Tylenchulus);剑线虫,剑线虫属(Xiphinema);以及其它植物寄生线虫属;
本发明混合物尤其适用于对抗鞘翅目、鳞翅目、缨翅目、同翅目、等翅目和直翅目的害虫。
它们也适用于防治以下植物寄生线虫,根结线虫属(Meloidogyne)、球胞囊线虫属(Globodera)、胞囊线虫属(Heterodera)、穿孔线虫属(Radopholus)、盘旋线虫属(Rotylenchus)、短体线虫属(Pratylenchus)和其它属。
对于种子处理而言,合适目标为各种作物种子、水果类、蔬菜、香料和观赏植物种子,例如玉米/玉蜀黍(甜和野生)、硬粒小麦、大豆、小麦、大麦、燕麦、黑麦、黑小麦、香蕉、稻、棉花、向日葵、土豆、牧草、苜蓿、草、草皮、高粱、油菜籽、芸苔属(Brassica spp.)、甜菜、茄子、西红柿、莴苣、卷心莴苣、胡椒、黄瓜、南瓜、甜瓜、菜豆、干豆、豌豆、韭菜、大蒜、洋葱、甘蓝菜、胡萝卜、块茎如甘蔗、烟草、咖啡、草皮和草料、十字花科植物、葫芦、葡萄藤、胡椒、饲料甜菜、油菜、三色堇、凤仙花属、矮牵牛和天竺葵。
术语种子处理包括本领域已知的所有合适的种子处理技术,例如包括但不限于拌种、种子包衣、种子撒粉、种子浸泡、种子涂膜、种子多层涂覆、种子包壳、种子滴淋和种子造粒。
本发明的活性成分混合物对于油菜、小麦、玉米、黑麦、大麦、燕麦、高梁、向日葵、稻、玉蜀黍、草皮和草料、棉花、甜菜、菜豆、豌豆、大豆、观赏植物和蔬菜(如葫芦、西红柿、茄子、土豆、胡椒、莴苣、甘蓝菜、胡萝卜、十字花科植物)的种子处理特别有利。
特别优选油菜、小麦、豆、玉米、大豆、棉花、高粱、甜菜、稻、蔬菜和观赏植物的种子处理。
本发明混合物最优选用于油菜的种子处理。
此外,本发明混合物也可用于因包括遗传工程方法在内的育种而耐受除草剂或杀真菌剂或杀虫剂的作用的作物。
例如,本发明混合物可用于转基因作物,该作物对选自磺酰脲类、咪唑啉酮类或草铵膦(glufosinate-ammonium)或草甘膦(glyphosateisopropylammonium)和类似活性物质的除草剂具有抗性(参见例如EP-A242 236、EP-A 242 246)(WO 92/00377)(EP-A 257 993、US 5,013,659),或用于转基因作物植物,例如棉花的种子,它们产生芽孢杆菌(Bacillusthuringiensis)毒素(Bt毒素)并且因此对某些害虫具有抗性(EP-A 142 924、EP-A 193 259)。
此外,本发明混合物也可用于处理与现有植物相比具有改进性能的植物的种子,后者可通过例如传统育种方法和/或产生突变体,或通过重组程序而产生。例如,对于改变植物中合成的淀粉(例如WO 92/11376、WO92/14827、WO 91/19806)或具有改变的脂肪酸组成的转基因作物植物(WO91/13972),已描述关于作物植物的重组改性的许多案例。
式I化合物和化合物II以及任选的其它活性成分可同时,即联合地或分别地或依次施用;在分开施用的情况下,施用顺序一般对防治措施的结果无任何影响。
式I化合物和化合物II通常以有效量施用,其重量比优选100∶1-1∶100,尤其是20∶1-1∶20,优选10∶1-1∶10。
式I化合物及其他杀真菌剂通常以有效量施用,优选以1000∶1-1∶1000的重量比施用。
取决于所需效果,尤其在农业栽培领域的情况下,本发明混合物的施用率为5-2000g/ha,优选50-1500g/ha,尤其是50-750g/ha。
此处,式I化合物的施用率为1g至1kg/ha,优选10-900g/ha,尤其是20-750g/ha。
相应地,化合物II的施用率为1g至1kg/ha,优选10-750g/ha,尤其是20-500g/ha。
相应地,其他杀真菌剂的施用率为1g至1kg/ha,优选5-900g/ha,尤其是10-750g/ha。
在处理种子中,本发明混合物的施用率一般为3kg:30g活性成分/100kg、100g:1g活性成分/100kg、30g:3kg活性成分/100kg或1g:100g活性成分/100kg。对于一些特定作物种子,如莴苣或洋葱,施用率可更高。
本发明的另一实施方案涉及用本发明混合物处理的种子。
本发明的活性成分混合物具有非常有利的治疗、预防和内吸杀真菌性能以保护栽培植物。如上所述,这些活性成分混合物可用于抑制或破坏不同作物或有用植物的植物或植物部分(果实、花、叶、茎、块茎、根)上所出现的病原体,同时保护那些后来生长出的植物部分防止这些病原体侵袭。活性成分混合物对主要出现于植物发育早期的土壤中的病害具有高活性的特殊优点。
在防治植物病原性有害真菌和/或有害昆虫和/或线虫时,尤其在防治植物病原性有害真菌和/或有害昆虫时,式I化合物和化合物II以及任选其它活性成分或本发明混合物的分开或联合施用通过在植物播种前或播种后或在植物出苗前或出苗后处理种子、植物或土壤而进行。
活性化合物和本发明混合物可例如制备成直接可喷雾溶液、粉末和悬浮液的形式或制备成高度浓缩水性、油性或其它悬浮液、分散体、乳液、油分散体、糊、粉剂、撒播用组合物或颗粒的形式,并可通过喷雾、雾化、撒粉、播撒或浇水,或直接或以水基浆料形式用种子处理机施用的着色悬浮液、溶液、乳液而施用。施用形式取决于特定目的;在每种情况下,其应确保本发明混合物尽可能精细且均匀的分布。
活性化合物和混合物可转化为常规配制剂,例如溶液、乳液、悬浮液、粉剂、粉末、糊和颗粒。使用形式取决于特定的目的;在每种情况下应确保本发明化合物精细和均匀地分布。
配制剂以已知方式制备,例如通过将活性化合物适用于配制农用化学品的助剂如溶剂和/或载体,以及需要的话乳化剂、表面活性剂和分散剂、防腐剂、消泡剂、防冻剂混合而制备,对于种子处理配制剂还任选有着色剂和/或粘合剂和/或胶凝剂(例如参见综述US 3,060,084、EP-A 707 445(对于液体浓缩物),Browning,“Agglomeration”,Chemical Engineering,1967年12月4日,147-48,Perry’s Chemical Engineer’s Handbook,第4版,McGraw-Hill,New York,1963,第8-57页及随后各页。WO 91/13546;US 4,172,714;US 4,144,050;US 3,920,442;US 5,180,587;US 5,232,701;US 5,208,030;GB 2,095,558;US 3,299,566,Klingman,Weed Control asa Science(杂草防治科学),John Wiley and Sons,Inc.,New York,1961,Hance等,Weed Control Handbook(杂草防治手册),第8版,BlackwellScientific Publications,Oxford,1989和Mollet,H.,Grubemann,A.,Formulation technology(配制技术),Wiley VCH Verlag GmbH,Weinheim(德国),2001,2.D.A.Knowles,Chemistry and Technology of AgrochemicalFormulations(农业化学配制剂化学和技术),Kluwer Academic Publishers,Dordrecht,1998(ISBN 0-7514-0443-8)。
合适的溶剂为水、芳族溶剂(如Solvesso产品、二甲苯)、石蜡(如矿物油馏分)、醇类(如甲醇、丁醇、戊醇、苄醇)、酮类(如环己酮、γ-丁内酯)、吡咯烷酮(NMP、NOP)、乙酸酯(乙二醇二乙酸酯)、二元醇、脂肪酸二甲基酰胺、脂肪酸及脂肪酸酯。原则上还可以使用溶剂混合物。
合适乳化剂为非离子和阴离子乳化剂(例如聚氧乙烯脂肪醇醚、烷基磺酸盐和芳基磺酸盐)。
分散剂的实例为木素亚硫酸盐废液和甲基纤维素。
适合使用的表面活性剂是木素磺酸、萘磺酸、苯酚磺酸、二丁基萘磺酸的碱金属盐、碱土金属盐和铵盐,烷基芳基磺酸盐,烷基硫酸盐,烷基磺酸盐,脂肪醇硫酸盐,脂肪酸和硫酸化脂肪醇乙二醇醚,还有磺化萘和萘衍生物与甲醛的缩合物,萘或萘磺酸与苯酚和甲醛的缩合物,聚氧乙烯辛基酚醚,乙氧基化异辛基酚、辛基酚、壬基酚,烷基酚聚乙二醇醚,三丁基苯基聚乙二醇醚,三硬脂基苯基聚乙二醇醚,烷基芳基聚醚醇,醇和脂肪醇/氧化乙烯缩合物,乙氧基化蓖麻油,聚氧乙烯烷基醚,乙氧基化聚氧丙烯,月桂醇聚乙二醇醚缩醛,山梨醇酯,木素亚硫酸盐废液和甲基纤维素。
适于制备可直接喷雾溶液、乳液、糊或油分散体的物质是中沸点到高沸点的矿物油馏分,如煤油或柴油,此外还有煤焦油和植物或动物来源的油,脂族、环状和芳族烃,例如甲苯、二甲苯、石蜡、四氢化萘、烷基化萘或其衍生物、甲醇、乙醇、丙醇、丁醇、环己醇、环己酮、异佛尔酮,强极性溶剂,例如二甲亚砜、N-甲基吡咯烷酮或水。
防冻剂如甘油、乙二醇、丙二醇以及杀菌剂也可加入配制剂。
合适的消泡剂例如为基于聚硅氧烷或硬脂酸镁的消泡剂。
合适的防腐剂例如为双氯酚(Dichlorophen)和苯甲醇半缩甲醛。
种子处理配制剂可额外包含粘合剂和任选着色剂。
可添加粘合剂以改进活性材料在处理后对于种子的粘附。合适粘合剂为嵌段共聚物EO/PO表面活性剂,以及聚乙烯醇、聚乙烯吡咯烷酮、聚丙烯酸酯、聚甲基丙烯酸酯、聚丁烯、聚异丁烯、聚苯乙烯、聚乙烯胺、聚乙烯酰胺、聚乙烯亚胺()、聚醚、聚氨酯、聚乙烯基乙酸酯、纤基乙酸钠和衍生自这些聚合物的共聚物。
任选在配制剂中也包含着色剂。适用于种子处理配制剂的着色剂或染料为若丹明B、C.I.颜料红112、C.I.溶剂红1、颜料蓝15:4、颜料蓝15:3、颜料蓝15:2、颜料蓝15:1、颜料蓝80、颜料黄1、颜料黄13、颜料红112、颜料红48:2、颜料红48:1、颜料红57:1、颜料红53:1、颜料橙43、颜料橙34、颜料橙5、颜料绿36、颜料绿7、颜料白6、颜料棕25、碱性紫10、碱性紫49、酸性红51、酸性红52、酸性红14、酸性蓝9、酸性黄23、碱性红10、碱性红108。
粉末、撒播用材料和可撒粉产品可以通过将活性物质与固体载体混合或同时研磨而制备。
颗粒如涂覆颗粒、浸渍颗粒和均质颗粒可以通过将活性化合物与固体载体粘附而制备。固体载体的实例是矿土如硅胶、硅酸盐、滑石、高岭土、活性粘土(attaclay)、石灰石、石灰、白垩、红玄武土、黄土、粘土、白云石、硅藻土、硫酸钙、硫酸镁、氧化镁,磨碎的合成材料,肥料如硫酸铵、磷酸铵、硝酸铵、尿素,以及植物来源的产品如谷粉、树皮粉、木粉和坚果壳粉,纤维素粉和其它固体载体。
配制剂通常包含0.01-95重量%,优选0.1-90重量%活性化合物。活性化合物以90-100重量%,优选95-100重量%的纯度(根据NMR谱)使用。
对于种子处理,各种配制剂可在稀释2-10倍后得到活性化合物在即用制剂中的0.01-60重量%,优选0.1-40重量%的浓度。
式I化合物和混合物可以直接、以其配制剂形式或由其制备的使用形式,如可直接喷雾溶液、粉末、悬浮液或分散体、乳液、油分散体、糊、可撒粉产品、撒播用材料或颗粒,借助喷雾、雾化、撒粉、撒播或浇灌来使用。使用形式完全取决于意欲的目的;意欲在每种情况下确保本发明活性化合物的最佳可能分布。
含水使用形式可通过加入水由乳液浓缩物、糊或可湿性粉末(可喷雾粉末、油分散体)制备。为制备乳液、糊或油分散体,可借助湿润剂、增粘剂、分散剂或乳化剂将该物质直接或溶于油或溶剂中后在水中均化。或者还可以制备由活性物质、湿润剂、增粘剂、分散剂或乳化剂以及合适的话溶剂或油组成的浓缩物且该浓缩物适于用水稀释。
即用制剂中的活性化合物浓度可在较宽范围内变化。其通常为0.0001-10重量%,优选0.01-1重量%。
活性化合物还可成功地以超低容量法(ULV)使用,其中可以施用包含超过95重量%活性化合物的配制剂或甚至可以在没有添加剂的情况下施用活性化合物。
下列为配制剂实例:
1.用水稀释的用于叶面施用的产品
对于种子处理,这些产品可稀释或不经稀释而施用于种子。
A水溶性浓缩物(SL、LS)
将10重量份活性化合物溶于90重量份水或水溶性溶剂中。或者,加入湿润剂或其它助剂。活性化合物经水稀释溶解,以此方式得到具有10重量%活性化合物的配制剂。
B分散性浓缩物(DC)
将20重量份活性化合物溶于70重量份环己酮中并加入10重量份分散剂如聚乙烯基吡咯烷酮。用水稀释得到分散体,由此得到具有20重量%活性化合物的配制剂。
C乳油(EC)
将15重量份活性化合物溶于7重量份二甲苯中并加入十二烷基苯磺酸钙和蓖麻油乙氧基化物(在每种情况下为5重量份)。用水稀释得到乳液,由此得到具有15重量%活性化合物的配制剂。
D乳液(EW、EO、ES)
将25重量份活性化合物溶于35重量份二甲苯中并加入十二烷基苯磺酸钙和蓖麻油乙氧基化物(在每种情况下为5重量份)。借助乳化机(如Ultraturrax)将该混合物加入30重量份水中并制成均相乳液。用水稀释得到乳液,由此得到具有25重量%活性化合物的配制剂。
E悬浮液(SC、OD、FS)
在搅拌的球磨机中,将20重量份活性化合物粉碎并加入10重量份分散剂和湿润剂以及70重量份水或有机溶剂,得到细碎活性化合物悬浮液。用水稀释得到稳定的活性化合物悬浮液,由此得到具有20重量%活性化合物的配制剂。
F水分散性颗粒和水溶性颗粒(WG、SG)
将50重量份活性化合物细碎研磨并加入50重量份分散剂和湿润剂,借助工业装置(如挤出机、喷雾塔、流化床)将其制成水分散性或水溶性颗粒。用水稀释得到稳定的活性化合物分散体或溶液,由此得到具有50重量%活性化合物的配制剂。
G水分散性粉末和水溶性粉末(WP、SP、SS、WS)
将75重量份活性化合物在转子-定子磨机中研磨并加入25重量份分散剂、湿润剂和硅胶。用水稀释得到稳定的活性化合物分散体或溶液,由此得到具有75重量%活性化合物的配制剂。
凝胶配制剂(GF)
在搅拌的球磨机中,将20重量份活性化合物在添加10重量份分散剂,1重量份胶凝剂以及70重量份水或有机溶剂下研磨,得到细碎活性化合物悬浮液。用水稀释得到稳定的活性化合物悬浮液,由此得到具有20重量%活性化合物的配制剂。
2.不经稀释而叶面施用的产品。对于种子处理,这些产品可经稀释施用于种子。
I可撒粉粉末(DP、DS)
将5重量份活性化合物细碎研磨并与95重量份细碎高岭土充分混合。这得到具有5重量%活性化合物的可撒粉产品。
J颗粒(GR、FG、GG、MG)
将0.5重量份活性化合物细碎研磨并结合99.5重量份载体,由此得到具有0.5重量%活性化合物的配制剂。现行方法是挤出、喷雾干燥或流化床方法。这得到不经稀释而叶面施用的颗粒。
K ULV溶液(UL)
将10重量份活性化合物溶于90重量份有机溶剂如二甲苯中。这得到不经稀释而叶面施用的具有10重量%活性化合物的产品。
常用的种子处理配制剂例如包括可流动浓缩物FS、溶液LS、干处理用粉末DS、浆料处理用水分散性粉末WS、水溶性粉末SS和乳液ES与EC和凝胶配制剂GF。这些配制剂可以不经稀释的形式或以经稀释的形式施用于种子。施用于种子可在播种之前进行或直接施用于种子。
在优选实施方案中,将FS配制剂用于种子处理。FS配制剂通常可包含1-800g/l活性成分、1-200g/l表面活性剂、0-200g/l防冻剂、0-400g/l粘合剂、0-200g/l颜料和至多1升溶剂,优选水。
即用制剂中的活性化合物浓度可在较宽范围内变化。通常而言,其为0.0001-10%,优选0.01-1%。
活性化合物还可成功地以超低容量法(ULV)使用,其中可以施用包含超过95重量%活性化合物的配制剂或甚至可以在没有添加剂的情况下施用活性化合物。
可以将各种类型的油、润湿剂、辅助剂、除草剂、杀真菌剂、其它农药或杀菌剂加入活性化合物中,合适的话恰在紧临使用之前(桶混合)加入。这些试剂通常可以1∶100-100∶1,优选1∶10-10∶1的重量比与本发明试剂混合。
就此而言合适的辅助剂尤其为:有机改性的聚硅氧烷,例如BreakThru S醇烷氧基化物,例如AtplusAtplus MBAPlurafac LF和Lutensol ONEO/PO嵌段聚合物,例如PluronicRPE和Genapol醇乙氧基化物,例如Lutensol XP以及磺基琥珀酸二辛酯钠,例如Leophen
本发明混合物的测试显示这些混合物有效防治真菌和/或昆虫和/或线虫且有效改善植物的健康。
应用实施例
化合物和混合物的杀真菌作用由以下测试证实:
温室
制备:以数个步骤制备喷雾溶液:
制备储备溶液:将丙酮和/或DMSO与湿润剂/乳化剂Uniperol(基于乙氧基化烷基酚)的混合物(溶剂-乳化剂之比为99∶1(体积))加入25mg化合物中,总共得到10ml。接着加入水直至总体积为100ml。
用所述溶剂-乳化剂-水混合物将储备溶液稀释至给定浓度。
应用实施例1-对致病疫霉(Phytophthora infestans)引起的西红柿晚疫病的防治
使西红柿植物的幼秧苗在盆中生长。将这些植物用活性成分或其混合物的浓度如下表所述的含水悬浮液喷雾至滴流点。第二天将叶子用致病疫霉的含水孢子囊悬浮液接种。在接种后,立即将测试植物转移至潮湿室中。在18-20℃和接近于100%的相对湿度下6天后,以害病叶面积%肉眼评估叶片上真菌侵袭的程度。
将肉眼测定的侵染叶面积百分数转化成以未处理对照的%表示的效力。
使用Abbot公式按如下计算的效力(E):
E=(1-α/β)·100
α对应于处理植物的真菌侵染百分数,和
β对应于未处理(对照)植物的真菌侵染百分数。
效力为0表示处理植物的侵染水平相当于未处理的对照植物;效力为100表示处理植物未受侵染。
活性化合物组合的预期效力使用Colby公式[Colby S.R.,“计算除草剂组合的协同增效和拮抗响应”,Weeds(杂草),15,第20-22页,1967)]确定并与观察的效力比较。
Colby公式:E=x+y-x·y/100
E使用浓度为a和b的活性化合物A和B的混合物时的预期效力,以相对于未处理对照的%表示,
x使用浓度为a的活性化合物A时的效力,以相对于未处理对照的%表示,y使用浓度为b的活性化合物B时的效力,以相对于未处理对照的%表示。
表1A-单个活性化合物
表1B-本发明的来自表1A的活性化合物的混合物
编号 | 活性化合物的混合物浓度混合比 | 观察到的效力 | 计算的效力* |
8 | 表1,#I-245+锐劲特16+63ppm1∶4 | 22 | 0 |
9 | 表1,#I-113+锐劲特4+16ppm1∶4 | 78 | 22 |
10 | 表1,#I-113+吡虫啉4+16ppm1∶4 | 78 | 40 |
11 | 表1,#I-113+虫螨威 | 89 | 22 |
4+16ppm1∶4 |
应用实施例2-预防性防治青椒叶上的灰霉病(灰葡萄孢(Botrytis cinerea))
使青椒幼秧苗在盆中生长至2-3片叶阶段。将这些植物用活性成分或其混合物的浓度如下表所述的含水悬浮液喷雾至滴流点。第二天将处理植物用灰葡萄孢于2%生物麦芽水溶液中的孢子悬浮液。立即将测试植物转移至黑暗潮湿室中。在22-24℃和接近于100%的相对湿度下5天后,以害病叶面积%肉眼评估叶片上真菌侵袭的程度。
类似于实施例1进行评估。
表2A-单个活性化合物
编号 | 活性化合物 | 活性化合物在喷雾液中的浓度[ppm] | 效力,以未处理对照的百分数表示 |
12 | 对照(未处理) | - | (90%侵染) |
13 | 表1,#I-290 | 16 | 0 |
14 | 锐劲特 | 63 | 10 |
表2B-本发明的来自表2A的活性化合物的混合物
编号 | 活性化合物的混合物浓度混合比 | 观察到的效力 | 计算的效力* |
15 | 表1,#I-290+锐劲特16+63ppm1∶4 | 30 | 10 |
应用实施例3-治疗性防治大豆上由豆薯层锈菌(Phakopsora pachyrhizi)引起的大豆锈病
将盆植大豆秧苗的叶用豆薯层锈菌孢子接种。为确保人工接种成功,将植物转移至相对湿度为约95%和温度为23-27℃的潮湿室中放置24小时。第二天,将这些植物用活性成分浓度如下表所述的含水悬浮液喷雾至滴流点。使植物风干。接着将试验植物在温度为23-27℃且相对湿度为60-80%的温室中培育14天。以害病叶面积%肉眼评估叶片上真菌侵袭的程度。
类似于实施例1进行评估。
将化合物N-R′-2,2-二halo-1-R″环丙烷甲酰胺-2-(2,6-二氯-α,α,α-三氟-对甲苯基)腙(其中R′为乙基,halo为氯,和R″为甲基)编号为A.23-1。
表3A-单个活性化合物
表3B-本发明的来自表3A的活性化合物的混合物
编号 | 活性化合物的混合物浓度混合比 | 观察到的效力 | 计算的效力* |
21 | 表1,#I-245+A.23-116+63ppm1∶4 | 33 | 0 |
22 | 表1,#I-245+虫螨威4+16ppm1∶4 | 56 | 0 |
应用实施例4-杀真菌性防治由葡萄生单轴霉(Plasmopara viticola)引起的葡萄霜霉病
使葡萄插枝在盆中生长至4-5叶片阶段。用含有下表中所述浓度的活性成分或其混合物的含水悬浮液对这些植物喷雾至滴流点。使植物风干。第二天,用葡萄生单轴霉的含水孢子悬浮液通过将该悬浮液喷雾较低叶面处对植物接种。接着,立即将测试植物转移至温度为22-24℃且相对湿度接近于100%的潮湿室中放置24小时。随后在温度为20-25℃且相对湿度为约50-80%的温室中培育5天。为促进病害症状的发作,再次将植物转移至潮湿室中放置24小时。然后以害病叶面积%肉眼评估叶片上真菌侵袭的程度。
类似于实施例1进行评估。
表4A-单个活性化合物
表4B-本发明的来自表4A的活性化合物的混合物
编号 | 活性化合物的混合物浓度混合比 | 观察到的效力 | 计算的效力* |
31 | 表1,#I-9+锐劲特4+16ppm1∶4 | 22 | 0 |
32 | 表1,#I-9+氰氟虫胺4+16ppm1∶4 | 22 | 0 |
33 | 表1,#I-290+吡虫清4+16ppm1∶4 | 22 | 0 |
34 | 表1,#I-290+甲体氯氰菊酯16+63ppm1∶4 | 83 | 56 |
微滴定板测试
应用实施例5-在微滴定板测试中对晚疫病病原体致病疫霉的活性
制备10000mg活性成分/1L DMSO。将储备溶液移至微滴定板(MTP)上并使用用于真菌的基于豌豆汁的水性营养培养基稀释,并在第二步中用致病疫霉的含水游动孢子悬浮液稀释至规定活性化合物浓度。将微滴定板置于温度为18℃的水蒸气饱和室中。在接种后第7天,使用吸收光度计在405nm处测量MTP。
将测量的参数与不含活性化合物的对照方案的生长以及不含真菌和活性化合物的空白值比较,以确定各活性化合物中病原体的相对生长%。
类似于实施例1进行评估。
表5A-单个活性化合物
表5B-本发明的来自表5A的活性化合物的混合物
编号 | 活性化合物的混合物浓度混合比 | 观察到的效力 | 计算的效力* |
61 | 表1,#I-9+A.23-11+4ppm1∶4 | 91 | 69 |
62 | 表1,#I-110+锐劲特1+4ppm1∶4 | 92 | 22 |
63 | 表1,#I-110+吡虫啉1+4ppm1∶4 | 94 | 13 |
64 | 表1,#I-110+吡虫清1+4ppm1∶4 | 96 | 14 |
65 | 表1,#I-110+甲体氯氰菊酯1+4ppm1∶4 | 93 | 14 |
66 | 表1,#I-110+虫螨威1+4ppm1∶4 | 96 | 15 |
67 | 表1,#I-110+噻虫胺1+4ppm1∶4 | 93 | 10 |
68 | 表1,#I-110+A.23-11+4ppm1∶4 | 96 | 21 |
69 | 表1,#I-110+氰氟虫胺1+4ppm1∶4 | 93 | 13 |
70 | 表1,#I-113+锐劲特4+16ppm1∶4 | 96 | 28 |
编号 | 活性化合物的混合物浓度混合比 | 观察到的效力 | 计算的效力* |
71 | 表1,#I-113+吡虫啉4+16ppm1∶4 | 78 | 21 |
72 | 表1,#I-113+吡虫清4+16ppm1∶4 | 85 | 19 |
73 | 表1,#I-113+甲体氯氰菊酯4+16ppm1∶4 | 92 | 19 |
74 | 表1,#I-113+虫螨威4+16ppm1∶4 | 84 | 22 |
75 | 表1,#I-113+噻虫胺4+16ppm1∶4 | 84 | 21 |
76 | 表1,#I-113+A.23-14+16ppm1∶4 | 99 | 24 |
77 | 表1,#I-113+氰氟虫胺4+16ppm1∶4 | 71 | 22 |
78 | 表1,#I-245+锐劲特0.25+1ppm1∶4 | 67 | 10 |
79 | 表1,#I-245+吡虫啉0.25+1ppm1∶4 | 48 | 14 |
80 | 表1,#I-245+虫螨威0.25+1ppm1∶4 | 50 | 15 |
编号 | 活性化合物的混合物浓度混合比 | 观察到的效力 | 计算的效力* |
81 | 表1,#I-245+噻虫胺0.25+1ppm1∶4 | 41 | 12 |
82 | 表1,#I-245+A.23-10.25+1ppm1∶4 | 54 | 20 |
应用实施例6-在微滴定测试中对小麦壳针孢的活性
制备10000mg活性成分/1L DMSO。将储备溶液移至微滴定板(MTP)上并使用用于真菌的基于生物麦芽的水性营养培养基稀释,并在第二步中用小麦壳针孢的含水游动孢子悬浮液稀释至规定活性化合物浓度。将微滴定板置于温度为18℃的水蒸气饱和室中。在接种后第7天,使用吸收光度计在405nm处测量MTP。
将测量的参数与不含活性化合物的对照方案的生长以及不含真菌和活性化合物的空白值比较,以确定各活性化合物中病原体的相对生长%。
类似于实施例1进行评估。
表6A-单个活性化合物
编号 | 活性化合物 | 活性化合物在喷雾液中的浓度[ppm] | 效力,以未处理对照的百分数表示 |
83 | 表1,#I-9 | 16 | 12 |
84 | 表1,#I-245 | 16 | 4 |
85 | 甲体氯氰菊酯 | 63 | 9 |
86 | 氰氟虫胺 | 63 | 0 |
表6B-本发明的来自表6A的活性化合物的混合物
编号 | 活性化合物的混合物浓度混合比 | 观察到的效力 | 计算的效力* |
87 | 表1,#I-9+氰氟虫胺16+63ppm1∶4 | 39 | 12 |
88 | 表1,#I-245+甲体氯氰菊酯6+63ppm1∶4 | 37 | 13 |
89 | 表1,#I-245+氰氟虫胺6+63ppm1∶4 | 36 | 4 |
测试结果显示由于协同增效作用,与使用Colby公式预期的相比,本发明混合物显著更为有效。
Claims (14)
1.农药混合物,其包含:
a)至少一种选自式I-110、I-113、I-245和I-290的唑并嘧啶基胺:
和
b)至少一种化合物II,其选自下组:
A.2.氨基甲酸酯类:虫螨威;
A.3.合成除虫菊酯类:甲体氯氰菊酯;
A.5.烟碱受体激动剂/拮抗剂化合物:吡虫清、噻虫胺、吡虫啉;
A.6.GABA门控氯离子通道拮抗剂化合物:氯丹、硫丹、林丹、acetoprole、乙虫清、锐劲特、pyrafluprole、pyriprole、氟吡唑虫、5-氨基-1-(2,6-二氯-4-三氟甲基苯基)-4-三氟甲烷亚磺酰基-1H-吡唑-3-甲酰胺;和
A.14.钠通道阻断剂化合物:氰氟虫胺,
其中式I化合物和化合物II的重量比为10∶1-1∶10。
2.根据权利要求1的农药混合物,其中化合物II为虫螨威。
3.根据权利要求1的农药混合物,其中化合物II为甲体氯氰菊酯。
4.根据权利要求1的农药混合物,其中化合物II选自吡虫清、噻虫胺和吡虫啉。
5.根据权利要求1的农药混合物,其中化合物II为钠通道阻断剂化合物氰氟虫胺。
6.根据权利要求1的农药混合物,其中化合物II为锐劲特。
7.根据权利要求1-6中任一项的农药混合物,其进一步包含一种杀真菌剂。
8.一种改善植物健康的方法,其包括以任何所需顺序,同时,即联合或分开或依次施用有效量的根据权利要求1-7中任一项的混合物。
9.一种在植物、植物部分、种子或其生长场所中防治或预防真菌侵染的方法,其包括以任何所需顺序,同时,即联合或分开或依次施用协同增效有效量的根据权利要求1-7中任一项的混合物。
10.一种在植物、植物部分、种子或其生长场所中防治或预防有害昆虫或线虫的方法,其包括以任何所需顺序,同时,即联合或分开或依次施用协同增效有效量的根据权利要求1-7中任一项的混合物。
11.一种保护种子的方法,其包括在播种前和/或在预萌发后使种子与协同增效有效量的如权利要求1-7中任一项所定义的混合物接触。
12.一种处理植物繁殖材料的方法,其中用如权利要求1-7中任一项所定义的混合物处理所述植物繁殖材料。
13.一种处理种子的方法,其中以每100kg种子0.1g至5kg的量的根据权利要求1-7中任一项的混合物处理所述种子。
14.一种农药组合物,其包含液体或固体载体和根据权利要求1-7中任一项的混合物。
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Families Citing this family (15)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1380209B1 (en) * | 2001-04-17 | 2012-09-05 | Nihon Nohyaku Co., Ltd. | Pest control agent composition and method of using the same |
WO2008087182A2 (de) | 2007-01-19 | 2008-07-24 | Basf Se | Fungizide mischungen aus 1-methylpyrazol-4-ylcarbonsäureaniliden und azolopyrimidinylaminen |
WO2008092836A2 (en) * | 2007-01-30 | 2008-08-07 | Basf Se | Method for improving plant health |
AU2008300629B2 (en) | 2007-09-20 | 2014-04-03 | Basf Se | Combinations comprising a fungicidal strain and an active compound |
WO2010043639A2 (en) * | 2008-10-16 | 2010-04-22 | Basf Se | Pesticidal mixtures |
WO2010043553A1 (en) * | 2008-10-16 | 2010-04-22 | Basf Se | Pesticidal mixtures comprising metaflumizone and a fungicidal compound |
CN201712857U (zh) | 2010-05-10 | 2011-01-19 | S.C.约翰逊父子公司 | 用于挥发性材料的散发装置及其壳体和散发片 |
CN102415403B (zh) * | 2010-09-28 | 2013-12-25 | 南京华洲药业有限公司 | 一种含呋虫胺和速灭威的复合杀虫组合物及其用途 |
EP2460407A1 (de) | 2010-12-01 | 2012-06-06 | Bayer CropScience AG | Wirkstoffkombinationen umfassend Pyridylethylbenzamide und weitere Wirkstoffe |
CN102630693A (zh) * | 2012-03-28 | 2012-08-15 | 联保作物科技有限公司 | 一种杀虫组合物及其制剂和应用 |
CN103828821B (zh) * | 2012-11-27 | 2016-01-13 | 陕西汤普森生物科技有限公司 | 一种含唑嘧菌胺与甲氧基丙烯酸酯类的杀菌组合物 |
US9205163B2 (en) | 2012-11-27 | 2015-12-08 | S.C. Johnson & Son, Inc. | Volatile material dispenser |
US9278151B2 (en) | 2012-11-27 | 2016-03-08 | S.C. Johnson & Son, Inc. | Volatile material dispenser |
CN103250742B (zh) * | 2013-05-23 | 2014-08-06 | 苏州谷力生物科技有限公司 | 一种杀虫剂组合物 |
KR102377395B1 (ko) * | 2021-11-05 | 2022-03-22 | 주식회사 에스비티제약 | 살충제 및 이를 이용한 해충 구제 방법 |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0071792A2 (de) * | 1981-08-01 | 1983-02-16 | BASF Aktiengesellschaft | 7-Amino-azolo(1,5-a)pyrimidine, Verfahren zu ihrer Herstellung und diese enthaltende Fungizide |
Family Cites Families (38)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3060084A (en) * | 1961-06-09 | 1962-10-23 | Du Pont | Improved homogeneous, readily dispersed, pesticidal concentrate |
US3299566A (en) * | 1964-06-01 | 1967-01-24 | Olin Mathieson | Water soluble film containing agricultural chemicals |
US4144050A (en) * | 1969-02-05 | 1979-03-13 | Hoechst Aktiengesellschaft | Micro granules for pesticides and process for their manufacture |
US3920442A (en) * | 1972-09-18 | 1975-11-18 | Du Pont | Water-dispersible pesticide aggregates |
US4172714A (en) * | 1976-12-20 | 1979-10-30 | E. I. Du Pont De Nemours And Company | Dry compactible, swellable herbicidal compositions and pellets produced therefrom |
DE3338292A1 (de) * | 1983-10-21 | 1985-05-02 | Basf Ag, 6700 Ludwigshafen | 7-amino-azolo(1,5-a)-pyrimidine und diese enthaltende fungizide |
EP0192060B1 (de) * | 1985-02-04 | 1991-09-18 | Nihon Bayer Agrochem K.K. | Heterocyclische Verbindungen |
US5013659A (en) * | 1987-07-27 | 1991-05-07 | E. I. Du Pont De Nemours And Company | Nucleic acid fragment encoding herbicide resistant plant acetolactate synthase |
KR900003088B1 (ko) * | 1988-03-26 | 1990-05-07 | 재단법인 한국화학연구소 | 5-하이드록시피라졸 유도체 |
US5180587A (en) * | 1988-06-28 | 1993-01-19 | E. I. Du Pont De Nemours And Company | Tablet formulations of pesticides |
ATE208560T1 (de) * | 1989-08-30 | 2001-11-15 | Kynoch Agrochemicals Proprieta | Herstellung eines dosierungsmittels |
ES2091878T3 (es) * | 1990-10-11 | 1996-11-16 | Sumitomo Chemical Co | Composicion plaguicida. |
FR2684519B1 (fr) * | 1991-12-06 | 1994-01-28 | Rhone Poulenc Agrochimie | Association d'un fongicide de la famille des triazoles et d'imidacloprid. |
KR100500181B1 (ko) * | 1997-04-07 | 2005-07-12 | 니혼노야쿠가부시키가이샤 | 피라졸 유도체, 이의 제조방법, 중간체 및 이를 유효 성분으로서 함유하는 유해 생물 방제제 |
US6277856B1 (en) * | 1998-09-25 | 2001-08-21 | American Cynamid Co. | Fungicidal mixtures |
US6221890B1 (en) * | 1999-10-21 | 2001-04-24 | Sumitomo Chemical Company Limited | Acaricidal compositions |
DK1414302T3 (da) * | 2001-07-26 | 2007-06-18 | Basf Ag | 7-aminotriazolopyrimidiner til bekæmpelse af skadelige svampe |
EP1725559A2 (de) * | 2004-03-10 | 2006-11-29 | Basf Aktiengesellschaft | 5,6-dialkyl-7-amino-triazolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
EP1725561B1 (de) * | 2004-03-10 | 2010-07-07 | Basf Se | 5,6-dialkyl-7-aminotriazolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
ATE473227T1 (de) * | 2004-03-10 | 2010-07-15 | Basf Se | 5,6-dialkyl-7-amino-triazolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
US20080076785A1 (en) * | 2004-09-28 | 2008-03-27 | Carsten Blettner | 7-Aminomethyl-1,2,4-Triazolo[1,5-A]Pyrimidine Compounds And Their Use For Controlling Pathogenic Fungi |
US20080227796A1 (en) * | 2004-12-17 | 2008-09-18 | Basf Aktiengesellschaft | 7-Amino-6-Hetaryl-1,2,4-Triazolo[1,5-A]Pyrimidine Compounds and the Use Thereof for Controlling Pathogenic Fungi |
BRPI0608161A2 (pt) * | 2005-02-16 | 2010-11-09 | Basf Ag | compostos, processo para preparar os mesmos, agente, semente, e, processo para combater fungos nocivos fitopatogênicos |
DE102005007160A1 (de) * | 2005-02-16 | 2006-08-24 | Basf Ag | Pyrazolcarbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
CN101133059A (zh) * | 2005-03-01 | 2008-02-27 | 巴斯福股份公司 | 5,6-二烷基-7-氨基唑并嘧啶、其制备方法及其在防治病原性真菌中的用途以及包含这些化合物的组合物 |
WO2006092413A1 (de) * | 2005-03-01 | 2006-09-08 | Basf Aktiengesellschaft | 5,6-dialkyl-7-amino-azolopyrimidine, verfahren zu ihrer herstellung und ihre verwendung zur bekämpfung von schadpilzen sowie sie enthaltende mittel |
JP2008532944A (ja) * | 2005-03-01 | 2008-08-21 | ビーエーエスエフ ソシエタス・ヨーロピア | 5,6−ジアルキル−7−アミノアゾロピリミジン、それらの製造方法、有害な菌類を防除するためのそれらの使用、およびそれらの化合物を含む物質 |
JP2008536805A (ja) * | 2005-03-01 | 2008-09-11 | ビーエーエスエフ ソシエタス・ヨーロピア | 5,6−ジアルキル−7−アミノアゾロピリミジン、それらの製造方法、植物病原性菌類を防除するためのそれらの使用、およびそれらを含む薬剤 |
CN101163404A (zh) * | 2005-04-25 | 2008-04-16 | 巴斯福股份公司 | 5-烷基-6-苯基烷基-7-氨基唑并嘧啶的用途、新的唑并嘧啶、其制备方法以及包含它们的组合物 |
JP2009502862A (ja) * | 2005-07-27 | 2009-01-29 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌剤5−アルキル−6−フェニルピラゾロピリミジン−7−イルアミン |
EP1910371A1 (de) * | 2005-07-27 | 2008-04-16 | Basf Se | Fungizide 5-methyl-6-phenyl-pyrazolopyrimidin-7-ylamine |
CA2616199C (en) * | 2005-07-27 | 2014-06-10 | Basf Aktiengesellschaft | Fungicidal mixtures based on azolopyrimidinylamines |
BRPI0613912A2 (pt) * | 2005-07-27 | 2016-11-22 | Basf Ag | compostos, processo para preparar compostos, agente fungicida, semente, e, método para combater fungos nocivos fitopatogênicos |
JP5618479B2 (ja) * | 2005-08-05 | 2014-11-05 | ビーエーエスエフ ソシエタス・ヨーロピアBasf Se | 置換1−メチルピラゾール−4−イルカルボキシアニリド類を含む殺菌性混合物 |
BRPI0710774A2 (pt) * | 2006-05-03 | 2011-06-21 | Basf Se | método para proteger plantas após germinação contra o ataque de fungos fitopatogênicos foliares, formulação para tratamento de semente, semente, e, uso de pelo menos um composto |
BRPI0713944A2 (pt) * | 2006-07-13 | 2012-12-04 | Basf Se | compostos, processo para preparar compostos, composição, semente e, processo para combater fungos nocivos fitopatogênicos |
WO2008087182A2 (de) * | 2007-01-19 | 2008-07-24 | Basf Se | Fungizide mischungen aus 1-methylpyrazol-4-ylcarbonsäureaniliden und azolopyrimidinylaminen |
EP1952690A3 (en) * | 2007-01-31 | 2009-04-22 | Basf Se | Pesticidal mixtures based on triazolopyrimidines and insecticides |
-
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Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0071792A2 (de) * | 1981-08-01 | 1983-02-16 | BASF Aktiengesellschaft | 7-Amino-azolo(1,5-a)pyrimidine, Verfahren zu ihrer Herstellung und diese enthaltende Fungizide |
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US20100093531A1 (en) | 2010-04-15 |
BRPI0806766A2 (pt) | 2011-09-13 |
CR10945A (es) | 2009-09-14 |
CL2008000240A1 (es) | 2008-05-30 |
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