CN115299444B - 一种包含三氟杀线酯的组合物和应用 - Google Patents
一种包含三氟杀线酯的组合物和应用 Download PDFInfo
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- CN115299444B CN115299444B CN202110535003.5A CN202110535003A CN115299444B CN 115299444 B CN115299444 B CN 115299444B CN 202110535003 A CN202110535003 A CN 202110535003A CN 115299444 B CN115299444 B CN 115299444B
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- trifloxystrobin
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- DBHVHTPMRCXCIY-UHFFFAOYSA-N tyclopyrazoflor Chemical compound N1=C(Cl)C(N(C(=O)CCSCCC(F)(F)F)CC)=CN1C1=CC=CN=C1 DBHVHTPMRCXCIY-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/08—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings with oxygen as the ring hetero 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/42—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing within the same carbon skeleton a carboxylic group or a thio analogue, or a derivative thereof, and a carbon atom having only two bonds to hetero atoms with at the most one bond to halogen, e.g. keto-carboxylic acids
-
- 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
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/06—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings
- A01N43/12—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom five-membered rings condensed with a carbocyclic ring
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
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- 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
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
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- 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
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Abstract
本发明提供了一种包含三氟杀线酯的组合物和应用。该组合物包括式(I)所示的化合物,和至少一种化合物Ⅱ(杀虫剂),和/或至少一种化合物III(杀菌剂)。本发明提供的在特定的配比范围内表现出明显的增效作用,能够有效提高对害虫的防治效果;在应用中降低了农药的使用剂量,从而降低使用成本、降低了农药在作物上的残留量,增强了对环境的友好性,减少环境污染。另外,本发明提供的组合物中有效成分的作用机理不同,不存在交互抗性的问题,能够延缓害虫抗药性的发生,并提高对抗性种群的防治效果,还可以防治多种病虫害。
Description
技术领域
本发明涉及杀虫剂的复配组合物技术领域,具体涉及一种包含三氟杀线酯的组合物和应用。
背景技术
害虫防治领域中出现的一个典型问题为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物学影响,同时仍能容许有效的害虫防治。遭遇的另一个问题涉及需要具有有效对抗宽范围害虫的可得的害虫防治剂。还存在需要击倒(know-down)活性与长期防治结合,即快速作用与持久作用结合的害虫防治剂。与使用农药相关的另一困难是各种农药化合物的重复和单一施用在许多情况下导致害虫的快速选择性,害虫对所述活性成分己具有天然或适应的耐药性。因此,需要有助于防止或克服耐药性的害虫防治剂。
杀虫剂复配是解决上述问题的最为有效的办法之一,合理的化学杀虫杀螨剂复配具有扩大杀虫谱,提高防治效果,减少用药量,降低药害,减少残留,延缓害虫耐药性和抗药性的发生与发展等优点。
发明内容
本发明的目的是为了克服现有技术存在的技术问题,提供一种包含三氟杀线酯的组合物和用途,在减少用药量的基础上,满足目前农业生产的需要,扩大农药的防治谱,实现病虫害的同时防治。
已发现该目的部分或完全地通过下文定义的活性化合物的组合实现。
本发明第一方面提供一种包含三氟杀线酯的组合物,该组合物包括式(I)所示的化合物,
和至少一种选自如下列出的化合物Ⅱ:
Ⅱ-M.1烟碱乙酰胆碱受体激动剂:
Ⅱ-M.1A新烟碱类:氯噻啉、啶虫脒、可尼丁、烯啶虫胺、吡虫清、噻虫胺、呋虫胺、吡虫啉、硝胺烯啶、哌虫啶、环氧虫啶、氟吡呋喃酮、噻虫啉和噻虫嗪;或
Ⅱ-M.1A.1:1-[(6-氯-3-吡啶基)甲基]-2,3,5,6,7,8-六氢-9-硝基-(5S,8R)-5,8-环氧基-1H-咪唑并[1,2-a]氮杂;或
Ⅱ-M.1A.2:(2E-)-1-[(6-氯吡啶-3-基)甲基]-N’-硝基-2-亚戊基氨基胍;或
Ⅱ-M.1A.3:1-[(6-氯吡啶-3-基)甲基]-7-甲基-8-硝基-5-丙氧基-1,2,3,5,6,7-六氢咪唑并[1,2-a]吡啶;或
Ⅱ-M.1B氟啶虫胺腈;或
Ⅱ-M.1C烟碱;或
Ⅱ-M.1D三氟苯嘧啶、二氯噻吡嘧啶、Flupyrimin;
Ⅱ-M.2烟碱乙酰胆碱受体变构活化剂:多杀菌素和乙基多杀菌素;
Ⅱ-M.3钠通道调节剂:
Ⅱ-M.3A拟除虫菊酯类:右旋反式氯丙炔菊酯、高效氯氰菊酯、氟丙菊酯、丙烯除虫菊、右旋丙烯菊酯、右旋反式丙烯菊酯、氟氯菊酯、生物烯丙菊酯、联苯菊酯、2-环戊烯基生物烯丙菊酯、生物苄呋菊酯、乙氰菊酯、氟氯氰菊酯、高效氟氯氰菊酯、(RS)氯氟氰菊酯、氯氟氰菊酯、精高效氯氟氰菊酯、氯氰菊酯、甲体氯氰菊酯、乙体氯氰菊酯、高效反式氯氰菊酯、己体氯氰菊酯、苯醚氰菊酯、溴氰菊酯、烯炔菊酯、高氰戊菊酯、醚菊酯、甲氰菊酯、杀灭菊酯、氟氰戊菊酯、氟氯苯菊酯、氟胺氰菊酯、溴氟醚菊酯、右旋七氟甲醚菊酯、咪炔菊酯、氯氟醚菊酯、甲氧苄氟菊酯、Momfluorothrin、Epsilon-metofluthrin、Epsilon-momfluorothrin、氯菊酯、苯醚菊酯、炔酮菊酯、丙氟菊酯、除虫菊酯(除虫菊)、灭虫菊、灭虫硅醚、七氟菊酯、四氟醚菊酯、胺菊酯、乙氰菊酯、苄螨醚、右旋炔丙菊酯、氟硅菊酯、右旋胺菊酯、四溴菊酯和四氟菊酯;或
Ⅱ-M.3B钠通道调节剂:滴滴涕和甲氧滴滴涕;或
Ⅱ-M.3C氰氟虫腙、茚虫威、藜芦碱;
Ⅱ-M.4双酰胺类的鱼尼汀受体调节剂:氟苯虫酰胺、氯氟氰虫酰胺、氯虫苯甲酰胺、溴氰虫酰胺、四氯虫酰胺、环丙虫酰胺、四唑虫酰胺、环溴虫酰胺、氟氰虫酰胺、氟氧虫酰胺、噻虫酰胺、硫虫酰胺、氟虫双酰胺,或邻苯二甲酰胺类化合物:
Ⅱ-M.4.1:(R)-3-氯-N1-{2-甲基-4-[1,2,2,2-四氟-1-(三氟甲基)乙基]苯基}-N2-(1-甲基-2-甲基磺酰基乙基)邻苯二甲酰胺;或
Ⅱ-M.4.2:(S)-3-氯-N1-{2-甲基-4-[1,2,2,2-四氟-1-(三氟甲基)乙基]苯基}-N2-(1-甲基-2-甲基磺酰基乙基)邻苯二甲酰胺;或化合物
Ⅱ-M.4.3:2-[3,5-二溴-2-({[3-溴-1-(3-氯吡啶-2-基)-1H-吡唑-5-基])基}氨基)苯甲酰基]-1,2-二甲基肼羧酸甲酯;或选自M.4.4a)至M.4.4l)的化合物:
Ⅱ-M.4.4a)N-[4,6-二氯-2-[(二乙基-λ-4-亚硫烷基(Sulfanylidene))氨基甲酰基]苯基]-2-(3-氯-2-吡啶基)-5-三氟甲基吡唑-3-甲酰胺;
Ⅱ-M.4.4b)N-[4-氯-2-[(二乙基-λ-4-亚硫烷基)氨基甲酰基]-6-甲基苯基]-2-(3-氯-2-吡啶基)-5-三氟甲基吡唑-3-甲酰胺;
Ⅱ-M.4.4c)N-[4-氯-2-[(二-2-丙基-λ-4-亚硫烷基)氨基甲绊基]-6-甲基苯基]-2-(3-氛-2-吡啶基)-5-三氟甲基吡唑-3-甲酰胺;
Ⅱ-M.4.4d)N-[4,6-二氯-2-[(二-2-丙基-λ-4-亚硫烷基)氨基甲酰基]苯基]-2-(3-氯-2-吡啶基)-5-三氟甲基吡唑-3-甲酰胺;
Ⅱ-M.4.4e)N-[4,6-二氯-2-[(二乙基-λ-4-亚硫烷基)氨基甲酰基]-苯基]-2-(3-氯-2-吡啶基)-5-二氟甲基吡唑-3-甲酰胺;
Ⅱ-M.4.4f)N-[4,6-二溴-2-[(二-2-丙基-λ-4-亚硫烷基)氨基甲酰基]-苯基]-2-(3-氯-2-吡啶基)-5-三氟甲基吡唑-3-甲酰胺;
Ⅱ-M.4.4g)N-[4-氯-2-[(二-2-丙基-λ-4-亚硫烷基)氨基甲酰基]-6-氰基苯基]-2-(3-氯-2-吡啶基)-5-三氟甲基吡唑-3-甲酰胺;
Ⅱ-M.4.4h)N-[4,6-二溴-2-[(二乙基-λ-4-亚硫烷基)氨基甲酰基]-苯基]-2-(3-氯-2-吡啶基)-5-三氟甲基吡唑-3-甲酰胺;
Ⅱ-M.4.4i)N-[2-(5-氨基-1,3,4-噻二唑-2-基)-4-氯-6-甲基苯基]-3-溴-1-(3-氯-2-吡啶基)-1H-吡唑-5-甲酰胺;
Ⅱ-M.4.4j)3-氯-1-(3-氯-2-吡啶基)-N-[2,4-二氯-6-[[(1-氰基-1-甲基乙基)氨基]羧基]苯基]-1H-吡唑-5-甲酰胺;
Ⅱ-M.4.4k)3-溴-N-[2,4-二氯-6-(甲基氨基甲酰基)苯基]-1-(3,5-二氯-2-吡啶基)-1H-吡唑-5-甲酰胺;
Ⅱ-M.4.41)N-[4-氯-2-[[(1,1-二甲基乙基)氨基]羧基]]-6-甲基苯基]-1-(3-氯-2-吡啶基)-3-(氟甲氧基)-1H-吡唑-5-甲酰胺;
或选自如下列出的化合物:
Ⅱ-M.4.5:N-(2-氰基丙-2-基)-N-(2,4-二甲基苯基)-3-碘苯-1,2-二甲酰胺;或
Ⅱ-M.4.6:3-氯-N-(2-氰基丙-2-基)-N-(2,4-二甲基苯基)-苯-1,2-二甲酰胺;
Ⅱ-M.4.7a)1-(3-氯-2-吡啶基)-N-[4-氰基-2-甲基-6-[(甲基氨基)羧基]苯基]-3-[[5-(三氟甲基)-2H-四唑-2-基]甲基]-1H-吡唑-5-甲酰胺;或者
Ⅱ-M.4.7b)1-(3-氯-2-吡啶基)-N-[4-氰基-2-甲基-6-[(甲基氨基))基]苯基]-3-[[5-(三氟甲基)-1H-四唑-1-基]甲基]-1H-吡唑-5-甲酰胺;
Ⅱ-M.5GABA门控氯离子通道拮抗剂:
Ⅱ-M.5A有机氯化合物:毒杀芬、狄氏剂、七氯、灭蚁灵、艾氏剂、硫丹、氯丹、三氯杀螨醇;或
Ⅱ-M.5B苯基吡唑类:乙虫腈、丁虫腈、氟虫腈、吡嗪氟虫腈、吡啶氟虫腈、乙酰虫腈、丁烯氟虫腈、Pyrafluprole和Pyriprole;
Ⅱ-M.5C异噁唑类:氟噁唑酰胺、氟雷拉纳、阿福拉纳、沙罗拉纳、洛替拉纳、异噁唑虫酰胺;
Ⅱ-M.5D:间双酰胺类:溴虫氟苯双酰胺、环丙氟虫胺;
Ⅱ-M.6选择性同翅目昆虫进食阻断剂:双丙环虫酯、吡蚜酮、拒嗪酮、氟啶虫酰胺、Pyrifluquinazon;
Ⅱ-M.7乙酰胆碱酯酶抑制剂
Ⅱ-M.7A氨基甲酸酯类:涕灭威、棉铃威、丙硫克百威、甲萘威、虫螨威、丁硫克百威、灭虫威、灭多虫、甲氨叉威、抗蚜威、残杀威、硫双威、灭害威、噁虫威、丁叉威、氧丁叉威、虫螨威、丁酮砜威、西维因、克百威、乙硫甲威、仲丁威、伐虫脒、呋线威、异丙威、灭多威、速灭威、杀线威、敌克威、混灭威、唑蚜威、灭除威、苯虫威、丁苯威、特氨叉威、混杀威、二甲威和灭杀威;或:
Ⅱ-M.7B有机磷酸酯类:噻唑膦、甲基异柳磷、硝虫硫磷、氯唑磷、高灭磷、乙基谷硫磷、辛硫磷、谷硫磷、苯硫磷、灭克磷、氨磺磷、毒虫畏、毒死蜱、甲基毒死蜱、庚虫磷、Imicyafos、甲基内吸磷、二嗪农、二溴磷、敌敌畏、百治磷、乐果、甲基乙拌磷、克线磷、乙硫磷、倍硫磷、异噁唑磷、马拉硫磷、灭蚜磷、甲胺磷、杀扑磷、速灭磷、久效磷、氧乐果、砜吸磷、一六零五、甲基一六零五、甲基对硫磷、稻丰散、甲拌磷、伏杀磷、亚胺硫磷、磷胺、虫螨磷、丙溴磷、烯虫磷、丙硫磷、喹硫磷、特丁磷、乙酰甲胺磷、甲基吡噁磷、益棉磷、保棉磷、吡唑硫磷、喹恶磷、打杀磷、硫特普、硫甲双磷、嘧丙磷、硫线磷、氯氧磷、氯甲硫磷、蝇毒磷、杀螟腈、杀螟松、特丁硫磷、沙虫畏、香芹油、香茅油、三唑磷、丙胺磷、0-(甲氧基氨硫代磷酰基)水杨酸异丙酯、敌百虫、唑啶磷、壤虫氯磷、氯甲磷、甲基毒虫畏、噻唑酮磷、蚜灭多;
Ⅱ-M.8氯离子通道激动剂:阿维菌素和米尔贝霉素:甲氨基阿维菌素苯甲酸盐(甲维盐)、伊维菌素、弥拜菌素、齐墩螨素、雷皮菌素和米尔螨素、阿维菌素B2;
Ⅱ-M.9保幼激素模拟物:蒙五一二、蒙七七七、烯虫炔酯、蒙五一五、双氧威、蚊蝇醚、烯虫乙酯、烯虫酯、苯氧威、吡丙醚;
Ⅱ-M.10螨生长抑制剂:四螨嗪、噻螨酮、特苯噁唑、氟螨嗪;
Ⅱ-M.11线粒体ATP合成酶抑制剂:杀螨硫隆、杀螨锡、唑环锡、三环锡、克螨特、三氯杀螨砜、三唑锡、苯丁锡、丁醚脲、二环己基碳二亚胺、炔螨特、4,6-二硝基邻甲酚(DNOC);
Ⅱ-M.12经由质子梯度干扰的氧化磷酸化去偶剂:虫螨腈、氟唑虫清、二硝甲酚、氟虫胺;
Ⅱ-M.13烟碱乙酰胆碱受体通道阻断剂:杀虫磺、巴丹、硫环杀、杀虫单、杀螟丹、杀虫环、杀虫双;
Ⅱ-M.14苯甲酰脲类的几丁质生物合成类型0抑制剂,包含双三氟虫脲、定虫隆、氟脲杀、氟螨脲、氟虫脲、氟铃脲、氟丙氧脲、双苯氟脲、多氟脲、伏虫隆、杀虫隆、氟啶脲、除虫脲、氟环脲、虱螨脲、氟酰脲、杀铃脲;
Ⅱ-M.15几丁质生物合成类型1抑制剂:噻嗪酮;
Ⅱ-M.16蜕皮干扰剂:灭蝇胺、乙螨唑、KK-42;
Ⅱ-M.17蜕皮激素受体激动剂:甲氧苯酰肼、双苯酰肼、特丁苯酰肼、呋喃虫酰肼、环虫酰肼、环氧酰肼、甲氧虫酰肼、虫酰肼、印楝素;
Ⅱ-M.18章鱼胺受体激动剂:双甲脒(虫螨脒);
Ⅱ-M.19线粒体配合物电子传输抑制剂:
Ⅱ-M.19.A线粒体配合物I电子传输抑制剂类:哒螨灵、喹螨醚、唑螨酯、嘧胺苯醚、哒螨酮、吡螨胺、嘧螨醚、唑虫酰胺、嘧虫胺、鱼藤酮;
Ⅱ-M.19.B线粒体配合物III电子传输抑制剂类:Flometoquin、灭蚁腙、灭螨醌、嘧螨酯、嘧螨胺、抗霉素;
Ⅱ-M.20电压依赖性钠通道阻断剂:噁二唑虫、氰氟虫胺、2-[2-(4-氰基苯基)-1-[3-(三氟甲基)苯基]亚乙基]-N-[4-(二氟甲氧基)苯基]氨基脲、N-(3-氯-2-甲基苯基)-2-[(4-氯苯基)[4-[甲基(甲基磺酰基)氨基]苯基]亚甲基]氨基脲;
Ⅱ-M.21乙酰CoA羧化酶抑制剂:包括特窗酸和特拉姆酸衍生物,包括螺螨酯、螺甲螨酯、螺虫乙酯、甲氧哌啶乙酯;
Ⅱ-M.22线粒体复合体IV电子传输抑制剂:
Ⅱ-M.22.A含磷化合物:磷化铝、磷化氢、磷化钙、膦和磷化锌;
Ⅱ-M.22.B氰化物;
Ⅱ-M.23β-酮腈衍生物类别的线粒体复合体II电子传输抑制剂:丁氟螨酯、腈吡螨酯、乙唑螨腈、氟吡甲酰胺;
Ⅱ-M.24混杂非特异性(多位点)抑制剂:
Ⅱ-M.24.A烷基卤:甲基溴、其他烷基卤;
Ⅱ-M.24.B氯化苦、硫酰氟、硼砂、吐酒石;
Ⅱ-M.24.C释放异硫氰酸甲酯:棉隆、威百亩;
Ⅱ-M.25生物胺受体竞争剂类化合物:双甲脲、苯甲醛腙、苯甲醛半卡巴腙;
Ⅱ-M.26神经细胞抑制剂:联苯肼酯;
Ⅱ-M.27顺乌头酸抑制剂:氟乙酸;
Ⅱ-M.28昆虫中肠膜微生物紊乱剂:蜡质芽孢杆菌、坚强芽孢杆菌、枯草芽孢杆菌、苏云金杆菌或球形芽孢杆菌及其产生的杀虫蛋白,如苏云金杆菌Israelensis亚种、苏云金杆菌Aizawai亚种、苏云金杆菌Kurstaki亚种、苏云金杆菌Tenebrionis亚种,或Bt作物蛋白:Cry1Ab、Cry1Ac、Cry1Fa、Cry2Ab、mCry3A、Cry3Ab、Cry3Bb和Cry34/35Ab1;
Ⅱ-M.29寄生性真菌:厚孢轮枝菌、淡紫拟青霉、厚垣孢普克尼亚菌、淡紫紫孢菌、白僵菌、绿僵菌;
Ⅱ-M.30未知或不确定作用模式的杀虫或杀线虫活性化合物:氰氨化钙、石灰氮、氨基寡糖素、异硫氰酸烯丙酯、嗜硫小红卵菌HNI-1、二甲基二硫、二甲基二硫醚、噁线硫醚、三氟吡啶胺、1,3-二氯丙烯、α-三噻吩、氟烯线砜、三氟咪啶酰胺、糠醛、蓖麻碱、二硫氰基甲烷、磺胺螨酯、苯螨特、溴螨酯、喹菌酮、冰晶石、苦参碱、藜芦碱、松螨鲨、橄榄鲨、螺螨双酯、氟螨双醚、嘧虫胺、氟噻虫砜、Fluhexafon、噁虫酮、硫酰氟、氟螨嗪、灭螨猛、啶虫丙醚、嗪虫唑酰胺、Pyflubumide、Flupentiofenox、Pyrifluquinazon、Tioxazafen、Benzpyrimoxan、Tyclopyrazoflor、Nicofluprole、Oxazosulfyl、Spidoxamat、Acynonapyr、Cyclobutrifluram、Dimpropyridaz、噻唑烷基吡啶胺类化合物:(6-甲氧基-N-((噻唑-5-基)甲基)-N-甲基-3-硝基吡啶-2-胺、6-甲氧基-N-((噻唑-5-基)甲基)-N-乙基3-硝基吡啶-2-胺、6-甲氧基-N-((5-溴噻唑-4-基)甲基)-N-乙基-3-硝基吡啶-2-胺);
和/或至少一种选自如下列出的化合物III:
III-F.I呼吸抑制剂
III-F.I1配合物III在Qo位点的抑制剂:腈嘧菌酯、嘧菌酯、丁香菌酯、甲香菌酯、醚菌胺、醚菌酯、吡唑醚菌酯、烯肟菌酯、烯肟菌胺、氟菌螨酯、氟嘧菌酯、亚胺菌、叉氨苯酰胺、肟醚菌胺、啶氧菌酯、唑菌胺酯、唑胺菌酯、唑菌酯、氯啶菌酯、苯氧菌胺、恶唑菌酮、甲酰胺、吡菌苯威、肟菌酯;
III-F.I2配合物III在Qi位点的抑制剂:氰霜唑、吲哚磺菌胺;
III-F.I3配合物I I抑制剂:麦锈灵、苯丙烯氟菌唑、啶酰菌胺、萎锈灵、呋菌胺、氟吡菌酰胺、甲呋酰胺、噻呋酰胺、氟酰胺、氟唑菌酰胺、氟唑菌酰羟胺、苯丙烯氟菌唑、联苯吡菌胺、呋吡菌胺、呋吡唑灵、Isofetamid、吡唑萘菌胺、丙氧灭绣胺、氧化萎锈灵、氟唑菌苯胺、吡噻菌胺、氟唑环菌胺、叶枯酞、溴氟唑菌;
III-F.I4其他呼吸抑制剂:二氟林;硝基苯基衍生物:乐杀螨、敌螨通、敌螨普、氟啶胺;嘧菌腙;有机金属化合物:薯瘟锡、三苯锡氯和毒菌锡;唑嘧菌胺;和硅噻菌胺、灭锈胺、嘧菌环胺;
III-F.II甾醇生物合成抑制剂:
III-F.II1 C14脱甲基酶抑制剂:
三唑类:戊环唑、双苯三唑醇、糠菌唑、环唑醇、噁醚唑、烯唑醇、精烯唑醇、氧唑菌、腈苯唑、喹唑菌酮、氟硅唑、粉唑醇、已唑醇、酰胺唑、环戊唑醇、环戊唑菌、腈菌唑、噁咪唑、多效唑、戊菌唑、丙环唑、丙硫菌唑、硅氟唑、戊唑醇、氟醚唑、三唑酮、唑菌醇、戊叉唑菌、烯效唑、灭菌唑、三唑醇、叶菌唑、亚胺唑、乙环唑;
咪唑类:抑霉唑、稻瘟酯、丙氯灵、氟菌唑;
嘧啶类、吡啶类和哌嗪类:异嘧菌醇、氟苯嘧啶醇、啶斑肟、嗪氨灵;
III-F.II2δ14-还原酶抑制剂:吗菌灵、吗菌灵乙酸酯、丁苯吗啉、十三吗啉、哌丙灵、螺环菌胺、克啉菌、苯锈啶、粉病灵和螺噁茂胺;
III-F.II3 3-酮基还原酶抑制剂:环酰菌胺、胺苯吡菌酮;
III-F.III核酸合成抑制剂:
III-F.III1苯基酰胺类或酰基氨基酸类杀真菌剂:苯霜灵、精苯霜灵、甲霜灵、精甲霜灵和恶霜灵、噁霉灵;
III-F.III2其他:土菌消、辛噻酮、异噻菌酮、恶喹酸、磺嘧菌灵;
III-F.IV细胞分裂和细胞骨架抑制剂:
III-F.IV1选自如下类别的微管蛋白抑制剂:
苯并咪唑类和托布津类:噻菌灵、苯菌灵、多菌灵、麦穗宁、涕必灵和甲基硫菌灵;
III-F.IV2其他细胞分裂抑制剂:乙霉威、噻唑菌胺、戊菌隆、氟吡菌胺、苯酰菌胺、苯菌酮、氰烯菌酯;
III-F.V氨基酸和蛋白质合成抑制剂:
III-F.V1选自如下苯氨基嘧啶类别的蛋氨酸合成抑制剂:环丙嘧啶、甲氧苯唳菌、嘧菌胺和二甲嘧菌胺;
III-F.V2蛋白质合成抑制剂:灭瘟素、春雷素、水合春雷素、米多霉素、链霉素、土霉素、多氧霉素和井冈霉素;
III-F.VI信号转导抑制剂:
F.VI1 MAP/组氨酸蛋白激酶抑制剂:氟菌安、咯菌腈、异丙定、杀菌利、烯菌酮、拌种咯和氟噁菌;
III-F.VI2 G蛋白抑制剂:喹氧灵;
III-F.VII类脂和膜合成抑制剂:
F.VII1磷脂生物合成抑制剂:克瘟散、异稻瘟净、定菌磷、稻瘟灵;
F.VII2类脂过氧化:氯硝胺、氯甲氧苯、五氯硝基苯、四氯硝基苯、甲基立枯磷、联苯、地茂散和氯唑灵;
F.VII3磷脂生物合成和细胞壁沉积:烯酰吗啉、氟吗啉、双炔酰菌胺、丁吡吗啉、苯噻菌胺、异丙菌胺;
III-F.VII4影响细胞膜渗透性的化合物和脂肪酸:百维灵;
III-F.VII5脂肪酸酰胺水解酶抑制剂:氟噻唑吡乙酮;
III-F.VIII具有多位点作用的抑制剂:
III-F.VIII1无机活性物质:波尔多液(Bordeaux混合物)、醋酸铜、氢氧化铜、王铜、碱式硫酸铜和硫;
III-F.VIII2硫代-和二硫代氨基甲酸酯类:福美铁、代森锰锌、代森锰、威百亩、代森联、甲基代森锌、福美双、代森锌和福美锌;
III-F.VIII3选自如下邻苯二甲酰亚胺、硫酰胺和氯代腈类别的有机氯化合物:敌菌灵、百菌清、敌菌丹、克菌丹、灭菌丹、抑菌灵、双氯酚、六氯苯、五氯酚及其盐、四氯苯酞、对甲抑菌灵、乙烯利、菌核净、异菌脲、腐霉利、乙烯菌核利;
III-F.VIII4胍类及其他:胍、多果定、多果定游离碱、双胍盐、双胍辛胺、双胍辛醋酸盐、双胍辛胺三乙酸盐、双八胍盐、二噻农;
III-F.IX细胞壁合成抑制剂:
III-F.IX1葡聚糖合成抑制剂:井冈霉素和多氧霉素;
III-F.IX2黑素合成抑制剂:咯喹酮、三环唑、氯环丙酰胺、双氯氰菌胺和氰菌胺;
III-F.X植物防御诱发剂:
III-F.X1噻二唑素、噻菌灵、异噻菌胺、噻酰菌胺、调环酸钙;
III-F.X2膦酸酯类:藻菌磷、乙磷铝、亚磷酸及其盐、碳酸氢钾或钠;
III-F.XI未知作用模式:
环氟菌胺、棉隆、咪菌威、哒菌清、野燕枯、野燕枯甲基硫酸酯、二苯胺、氟联苯菌、磺菌胺、Flutianil、磺菌威、氯定、异丙消、Tolprocarb、喹啉铜、丙氧喹啉、Tebufloquin、叶枯酞、唑菌嗪。
根据本发明的一些实施方式,施用式(I)所示的化合物与至少一种化合物Ⅱ和/或Ⅲ。
根据本发明的一些实施方式,式(I)所示的化合物与化合物II和/或化合物Ⅲ的重量比为50:1-1:50,如50:1、45:1、40:1、35:1、30:1、25:1、20:1、15:1、10:1、5:1、1:1、1:5、1:10、1:15、1:20、1:25、1:30、1:35、1:40、1:45、1:50或上述数值之间的任意值。
优选的,式(I)所示的化合物与化合物II和/或化合物Ⅲ的重量比为30:1-1:10。
根据本发明的一些实施方式,所述组合物的剂型悬浮剂、悬乳剂、微乳剂、水分散粒剂、颗粒剂、烟剂、微囊悬浮剂、微囊悬浮-悬浮剂、种子处理剂、悬浮种衣剂、种子处理乳剂、种子处理粉剂、粉剂、干悬浮剂、乳油或水乳剂。
优选的,所述剂型为颗粒剂、种子处理剂、悬浮种衣剂或乳油。
本发明还提供一种防治昆虫、螨虫或线虫的方法,该方法包括使昆虫、螨虫、线虫或其食物供应链、栖息地、繁殖地以及其它场所与农药有效量的前述组合物接触。
本发明还提供一种保护植物繁殖材料的方法,该方法包括使植物繁殖材料与农药有效量的前述组合物接触。
本发明还提供一种种子制品,该种子制品包括种子以及含量为0.1g至100kg/100kg种子的前述组合物。
本发明还提供一种前述组合物在对抗昆虫、螨虫或线虫中的用途。
本发明还提供一种农药组合物,包含固体或液体载体以及前述组合物。
本发明还提供一种前述组合物在防治植物病虫害中的用途。
本发明具有如下优点:
本发明含有三氟杀线酯的杀虫杀菌组合物,以提高防效,降低用药量,同时解决杀虫杀螨单剂长期使用可能带来的抗性产生、药效下降等问题,以满足农业病虫害防治方面的需求。
本发明提供组合物的增效作用具体表现为:
1.本发明的组合物在一定配比范围内表现出明显的增效作用,提高了该化合物对害虫的防治效果。
2.该组合物在应用中降低了农药的使用剂量,从而降低使用成本,降低了农药在作物上的残留量,增强了对环境的友好性,减少环境污染。
3.该组合物各有效成分的作用机理不同,不存在交互抗性的问题,可以延缓害虫抗药性的发生,并提高对抗性种群的防治效果。
4.该组合物可以防治多种病虫害。
具体实施方式
下文将结合具体实施例对本发明做更进一步的详细说明。应当理解,下列实施例仅为示例性地说明和解释本发明,而不应被解释为对本发明保护范围的限制。凡基于本发明上述内容所实现的技术均涵盖在本发明旨在保护的范围内。
下述实施例中所使用的实验方法如无特殊说明,均为常规方法;下述实施例中所用的试剂、材料等,如无特殊说明,均可从商业途径得到。
下述实施例中计算处理药剂防治效果的公式如下:
病情分级标准:
0级:全株无病;
1级:第4张叶片及其以下各叶鞘、叶片发病(以顶叶为第1叶片);
3级:第3张叶片及其以下各叶鞘、叶片发病;
5级:第2张叶片及其以下各叶鞘、叶片发病;
7级:剑叶叶片及其以下各叶鞘、叶片发病;
9级:全株发病,提早枯死。
式中:
CK0-空白对照区施药前病情指数
CK1-空白对照区施药后病情指数
PT0-药剂处理区施药前病情指数
PT1-药剂处理区施药后病情指数
下述实施例的制剂中各组分如果没有特别的说明,均是指质量百分含量。
实施例
1)试验作物为柑橘
防治对象为柑橘全爪螨(Panonchus citri Mc Gregor)
田间药效试验参照《农药田间药效试验准则》进行。对照试药剂试验剂量为推荐剂量。设清水处理为空白对照,每个剂量处理4次重复,随机区组排列。将药剂均匀喷雾于植株枝条和叶片正反面,使螨充分接触药液。施药前调查虫口基数,施药后采用定点调查法,每小区调查2株植株,每株标记东、南、西、北、中五点,每点1梢,每梢调查5张叶片,每小区共调查50张叶片,记录活成、若螨数,于施药后14天调查结果,检查并记录叶片上活动态螨的数量,计算螨口减退率及处理药剂防治效果。结果见表1。
表1对柑橘全爪螨田间防效试验结果
供试药剂 | 浓度(mg/L) | 药后14天平均防效(%) |
5%三氟杀线酯(式(I)所示的化合物)乳油 | 50 | 93.54 |
15%哒螨灵微乳剂 | 50 | 82.34 |
22.4%螺虫乙酯(化合物II)悬浮剂 | 50 | 80.51 |
34%螺螨酯(化合物II)悬浮剂 | 50 | 76.24 |
20%丁氟螨酯(化合物II)悬浮剂 | 50 | 81.27 |
30%腈吡螨酯(化合物II)悬浮剂 | 50 | 70.34 |
30%乙螨唑(化合物II)悬浮剂 | 50 | 72.61 |
15%唑虫酰胺(化合物II)悬浮剂 | 50 | 65.29 |
43%联苯肼酯(化合物II)悬浮剂 | 50 | 63.11 |
10%阿维菌素(化合物II)悬浮剂 | 50 | 81.26 |
25%三唑锡(化合物II)悬浮剂 | 50 | 70.54 |
20%三氟杀线酯·哒螨灵乳油 | 25+25 | 98.26 |
25%三氟杀线酯·螺虫乙酯乳油 | 25+25 | 97.86 |
40%三氟杀线酯·螺螨酯乳油 | 25+25 | 98.47 |
25%三氟杀线酯·丁氟螨酯乳油 | 25+25 | 99.21 |
40%三氟杀线酯·腈吡螨酯乳油 | 25+25 | 96.13 |
40%三氟杀线酯·乙螨唑乳油 | 25+25 | 95.57 |
25%三氟杀线酯·唑虫酰胺乳油 | 25+25 | 95.17 |
50%三氟杀线酯·联苯肼酯乳油 | 25+25 | 96.26 |
20%三氟杀线酯·阿维菌素乳油 | 25+25 | 97.11 |
40%三氟杀线酯·三唑锡乳油 | 25+25 | 95.27 |
2)试验作物为火龙果
防治对象为刺足根螨(Rhizoglyphus echinopus)
田间药效试验参照《农药田间药效试验准则》进行。对照试药剂试验剂量为推荐剂量。设清水处理为空白对照,每个剂量处理4次重复,随机区组排列,每小区面积不少于15m2。施药时保证药量准确,分布均匀。施药前调查根螨基数,于施药后14天调查结果,寻找受害可疑病株,采用对角线五点取样法,每点调查两株,记录活成、若螨数,于施药后14天调查结果,检查并记录根部活动态螨的数量,计算螨口减退率及处理药剂防治效果。结果见表2。
表2对根螨田间防效试验结果
供试药剂 | 浓度(mg/L) | 药后14天平均防效(%) |
5%三氟杀线酯(式(I)所示的化合物)乳油 | 50 | 94.95 |
10%阿维菌素(化合物II)悬浮剂 | 50 | 88.56 |
15%哒螨灵(化合物II)微乳剂 | 50 | 76.54 |
48%毒死蜱(化合物II)乳油 | 50 | 88.99 |
40%辛硫磷(化合物II)乳油 | 50 | 63.24 |
73%炔螨特(化合物II)乳油 | 50 | 72.58 |
40%三氯杀螨醇(化合物II)乳油 | 50 | 78.36 |
5%噻螨酮(化合物II)乳油 | 50 | 86.51 |
20%双甲脒(化合物II)乳油 | 50 | 89.46 |
20%三氟杀线酯·阿维菌素颗粒剂 | 25+25 | 98.54 |
25%三氟杀线酯·哒螨灵颗粒剂 | 25+25 | 95.16 |
50%三氟杀线酯·毒死蜱颗粒剂 | 25+25 | 97.38 |
50%三氟杀线酯·辛硫磷颗粒剂 | 25+25 | 99.56 |
80%三氟杀线酯·炔螨特颗粒剂 | 25+25 | 98.57 |
50%三氟杀线酯·三氯杀螨醇颗粒剂 | 25+25 | 96.32 |
15%三氟杀线酯·噻螨酮颗粒剂 | 25+25 | 97.58 |
30%三氟杀线酯·双甲脒颗粒剂 | 25+25 | 96.39 |
3)试验作物为番茄
防治对象为南方根结线虫(Meloidogyne incognita(Kofold&White)Chitwood)
田间药效试验参照《农药田间药效试验准则》进行。对照试药剂试验剂量为推荐剂量。设清水处理为空白对照,每个剂量处理4次重复,随机区组排列,每小区面积不少于15m2。施药时保证药量准确,分布均匀。施药前调查线虫基数,于施药后14天调查结果,寻找受害可疑病株,采用对角线五点取样法,每点调查两株,计算发病率、病情指数和防治效果。结果见表3。
表3对根结线虫田间防效试验结果
供试药剂 | 浓度(mg/L) | 药后14天平均防效(%) |
5%三氟杀线酯(式(I)所示的化合物)乳油 | 50 | 92.77 |
3%噻虫啉微囊(化合物II)悬浮剂 | 50 | 77.86 |
20%甲氧虫酰肼(化合物II)悬浮剂 | 50 | 85.36 |
10%吡虫啉(化合物II)可湿性粉剂 | 50 | 89.54 |
20%氟啶虫酰胺(化合物II)悬浮剂 | 50 | 69.72 |
1%甲维盐(化合物II)乳油 | 50 | 79.58 |
15%哒螨灵(化合物II)微乳剂 | 50 | 86.91 |
40%氟烯线砜(化合物Ⅱ)乳油 | 50 | 85.39 |
500g/L三氟咪啶酰胺(化合物Ⅱ)悬浮剂 | 50 | 88.51 |
41.7%氟吡菌酰胺(化合物Ⅲ)悬浮剂 | 50 | 88.79 |
2.5%氟氯氰菊酯(化合物II)乳油 | 50 | 87.58 |
10%三氟杀线酯·噻虫啉颗粒剂 | 25+25 | 96.54 |
25%三氟杀线酯·甲氧虫酰肼颗粒剂 | 25+25 | 95.13 |
20%三氟杀线酯·吡虫啉颗粒剂 | 25+25 | 97.82 |
30%三氟杀线酯·氟啶虫酰胺颗粒剂 | 25+25 | 97.56 |
10%三氟杀线酯·甲维盐颗粒剂 | 25+25 | 96.19 |
25%三氟杀线酯·哒螨灵颗粒剂 | 25+25 | 98.63 |
50%三氟杀线酯·氟烯线砜颗粒剂 | 25+25 | 99.61 |
12%三氟杀线酯·三氟咪啶酰胺颗粒剂 | 25+25 | 98.54 |
50%三氟杀线酯·氟吡菌酰胺颗粒剂 | 25+25 | 99.56 |
10%三氟杀线酯·氟氯氰菊酯颗粒剂 | 25+25 | 99.51 |
4)试验作物为韭菜
防治对象为韭蛆(Bradysia odoriphaga Yang et Zhang)
田间药效试验参照《农药田间药效试验准则》进行。对照试药剂试验剂量为推荐剂量。设清水处理为空白对照,每个剂量处理4次重复,随机区组排列,每小区面积不少于15m2。施药时保证药量准确,分布均匀。施药前调查韭蛆基数,于施药后14天调查结果,在小区中心区刨出5穴韭菜,统计鳞茎内外活蛆数,计算防治效果。结果见表4。
表4对韭蛆田间防效试验结果
供试药剂 | 浓度(mg/L) | 药后14天平均防效(%) |
5%三氟杀线酯(式(I)所示的化合物)乳油 | 50 | 91.56 |
48%毒死蜱(化合物II)乳油 | 50 | 89.26 |
50%辛硫磷(化合物II)乳油 | 50 | 78.45 |
70%灭蝇胺(化合物II)可湿性粉剂 | 50 | 83.26 |
10%阿维菌素(化合物II)悬浮剂 | 50 | 84.63 |
1%甲维盐乳油 | 50 | 79.69 |
2.5%溴氰菊酯(化合物II)乳油 | 50 | 79.52 |
10%吡虫啉(化合物II)可湿性粉剂 | 50 | 89.65 |
25%噻虫嗪(化合物II)水分散粒剂 | 50 | 88.17 |
4.5%高效氯氰菊酯(化合物II)乳油 | 50 | 86.29 |
50%三氟杀线酯·毒死蜱颗粒剂 | 25+25 | 95.66 |
60%三氟杀线酯·辛硫磷颗粒剂 | 25+25 | 97.88 |
80%三氟杀线酯·灭蝇胺颗粒剂 | 25+25 | 96.35 |
20%三氟杀线酯·阿维菌素颗粒剂 | 25+25 | 96.98 |
10%三氟杀线酯·甲维盐颗粒剂 | 25+25 | 97.89 |
10%三氟杀线酯·溴氰菊酯颗粒剂 | 25+25 | 98.17 |
20%三氟杀线酯·吡虫啉颗粒剂 | 25+25 | 99.54 |
40%三氟杀线酯·噻虫嗪颗粒剂 | 25+25 | 96.31 |
15%三氟杀线酯·高效氯氰菊酯颗粒剂 | 25+25 | 97.65 |
5)试验作物为茄子
防治对象为西花蓟马(frankliniella occidentalis(Pergande))
田间药效试验参照《农药田间药效试验准则》进行。对照试药剂试验剂量为推荐剂量。设清水处理为空白对照,每个剂量处理4次重复,随机区组排列,每小区面积不少于20m2。将药剂均匀喷雾于植株枝条和叶片正反面,使西花蓟马充分接触药液。施药前调查虫口基数,施药后采用定点调查法,于茄子植株中、上部固定选取15片~30片叶,,记录活虫数,于施药后14天调查结果,检查并记录叶片上活动态螨的数量,计算蓟马减退率及处理药剂防治效果。结果见表5。
表5对西花蓟马田间防效试验结果
供试药剂 | 浓度(mg/L) | 药后14天平均防效(%) |
5%三氟杀线酯(式(I)所示的化合物)乳油 | 50 | 94.56 |
2.5%多杀菌素(化合物II)悬浮剂 | 50 | 78.66 |
1%甲维盐乳油 | 50 | 86.34 |
20%啶虫脒(化合物II)可湿性粉剂 | 50 | 88.56 |
10%吡虫啉(化合物II)可湿性粉剂 | 50 | 84.19 |
10%阿维菌素(化合物II)悬浮剂 | 50 | 79.66 |
10%虫螨腈(化合物II)悬浮剂 | 50 | 78.37 |
24%灭多威(化合物II)乳油 | 50 | 76.52 |
2.5%氟氯氰菊酯(化合物II)乳油 | 50 | 88.69 |
48%毒死蜱(化合物II)乳油 | 50 | 79.67 |
10%三氟杀线酯·多杀菌素乳油 | 25+25 | 98.65 |
10%三氟杀线酯·甲维盐乳油 | 25+25 | 99.62 |
30%三氟杀线酯·啶虫脒乳油 | 25+25 | 97.52 |
20%三氟杀线酯·吡虫啉乳油 | 25+25 | 98.13 |
20%三氟杀线酯·阿维菌素乳油 | 25+25 | 97.52 |
20%三氟杀线酯·溴虫腈乳油 | 25+25 | 97.51 |
30%三氟杀线酯·灭多威乳油 | 25+25 | 97.26 |
10%三氟杀线酯·氟氯氰菊酯乳油 | 25+25 | 98.16 |
50%三氟杀线酯·毒死蜱乳油 | 25+25 | 99.53 |
6)试验作物为甘蓝
防治对象为小菜蛾(Plutella xylostella(Linnaeus))
田间药效试验参照《农药田间药效试验准则》进行。对照试药剂试验剂量为推荐剂量。设清水处理为空白对照,每个剂量处理4次重复,随机区组排列,每小区面积不少于20m2。将药剂均匀喷雾于植株正反面,使小菜蛾充分接触药液。施药前调查虫口基数,施药后采用5点取样法,每小区5点取样,每点调查有虫株10株,施药后第14天调查各小区活虫数计算虫口减退率和防治效果。结果见表6。
表6对小菜蛾田间防效试验结果
7)试验作物为小麦
防治对象为禾缢管蚜(Rhopalosiphum padi)
田间药效试验参照《农药田间药效试验准则》进行。对照试药剂试验剂量为推荐剂量。设清水处理为空白对照,每个剂量处理4次重复,随机区组排列,每小区面积不少于20m2。施药时保证药量准确,分布均匀。施药前调查虫口基数,施药后采用5点取样法,每小区5点取样,每点调查有虫株10株,施药后第14天调查各小区活虫数计算虫口减退率和防治效果。结果见表7。
表7对蚜虫田间防效试验结果
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8)试验作物为玉米
防治对象为茎基腐病(菌种:禾谷镰孢菌Fusarium graminearum)
田间药效试验参照《农药田间药效试验准则》进行。对照试药剂试验剂量为推荐剂量。设清水处理为空白对照,每个剂量处理4次重复,随机区组排列,每小区面积不少于20m2。施药时保证药量准确,分布均匀。施药前调查病情基数,根据玉米叶鞘和叶片为害症状和程度分级,以株为单位,每小区采用对角线5点取样法,每点调查相连5丛,共25丛,记录总株数、病株数和病级数,施药后第14天调查防治效果。结果见表8。
表8对茎基腐病田间防效试验结果
供试药剂 | 浓度(mg/L) | 药后14天平均防效(%) |
5%三氟杀线酯(式(I)所示的化合物)乳油 | 50 | 91.85 |
20%精甲霜灵(化合物III)悬浮种衣剂 | 50 | 75.65 |
30%噁霉灵(化合物III)悬浮种衣剂 | 50 | 74.58 |
25g/L咯菌腈(化合物III)悬浮种衣剂 | 50 | 78.96 |
25%吡唑醚菌酯(化合物III)悬浮剂 | 50 | 84.57 |
70%甲基硫菌灵(化合物III)可湿性粉剂 | 50 | 79.61 |
50%福美双(化合物III)可湿性粉剂 | 50 | 74.68 |
80%克菌丹(化合物III)水分散粒剂 | 50 | 84.53 |
30%三氟杀线酯·精甲霜灵悬浮种衣剂 | 25+25 | 95.82 |
40%三氟杀线酯·噁霉灵悬浮种衣剂 | 25+25 | 97.61 |
35%三氟杀线酯·咯菌腈悬浮种衣剂 | 25+25 | 96.32 |
35%三氟杀线酯·吡唑醚菌酯悬浮种衣剂 | 25+25 | 94.13 |
80%三氟杀线酯·甲基硫菌灵悬浮种衣剂 | 25+25 | 95.61 |
60%三氟杀线酯·福美双悬浮种衣剂 | 25+25 | 96.32 |
90%三氟杀线酯·克菌丹悬浮种衣剂 | 25+25 | 95.46 |
9)试验作物为水稻
防治对象纹枯病(菌种:立枯丝核菌Rhizoctonia solani)
田间药效试验参照《农药田间药效试验准则》进行。对照试药剂试验剂量为推荐剂量。设清水处理为空白对照,每个剂量处理4次重复,随机区组排列,每小区面积不少于20m2。施药时保证药量准确,分布均匀。施药前调查病情基数,根据水稻叶鞘和叶片为害症状和程度分级,以株为单位,每小区采用对角线5点取样法,每点调查相连5丛,共25丛,记录总株数、病株数和病级数,施药后第14天调查防治效果。结果见表9。
表9对纹枯病田间防效试验结果
供试药剂 | 浓度(mg/L) | 药后14天平均防效(%) |
5%三氟杀线酯(式(I)所示的化合物)乳油 | 50 | 92.34 |
4%噻呋酰胺(化合物III)颗粒剂 | 50 | 89.56 |
1%粉唑醇(化合物III)颗粒剂 | 50 | 89.13 |
80%醚菌酯(化合物III)水分散粒剂 | 50 | 78.42 |
75%三环唑(化合物III)可湿性粉剂 | 50 | 79.25 |
10%三氟杀线酯·噻呋酰胺颗粒剂 | 25+25 | 95.63 |
10%三氟杀线酯·粉唑醇颗粒剂 | 25+25 | 96.58 |
90%三氟杀线酯·醚菌酯颗粒剂 | 25+25 | 94.32 |
80%三氟杀线酯·三环唑颗粒剂 | 25+25 | 98.17 |
结果如上各实施例所示,三氟杀线酯(式(I)所示的化合物与其他药剂(化合物II和/或化合物III)复配后,能够降低两者用药量,提高对害螨防效。
在施药到调查结束观察,均未发现实施例各制剂对作物产生可见的植物毒性症状,施药后的各作物生长良好。
应当理解的是,上述实施例是本发明的部分实施例,仅仅是为了更好的了解本发明的实施例而提供的,并不是本发明的所有实施例。实际应用中,通过调整本发明中上述各个组分的含量以及组分之间的组合方式,可以获得不同的、无数的实施例,这些均在本发明的涵盖范围内。
以上,对本发明的实施方式进行了说明。但是,本发明不限定于上述实施方式。凡在本发明的精神和原则之内,所做的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (7)
1.一种包含三氟杀线酯的组合物,其特征在于,该组合物由式(I)所示的化合物,
(I),
和化合物Ⅱ组成;其中,所述化合物II为噻虫胺、吡虫啉、啶虫脒或噻虫嗪;
其中,式(I)所示的化合物与化合物II的重量比为1:1。
2.根据权利要求1所述的组合物,其中,所述组合物的剂型为悬浮剂、悬乳剂、微乳剂、水分散粒剂、颗粒剂、烟剂、微囊悬浮剂、微囊悬浮-悬浮剂、悬浮种衣剂、种子处理乳剂、种子处理粉剂、粉剂、干悬浮剂、乳油或水乳剂。
3.一种防治昆虫或线虫的方法,其特征在于,该方法包括使昆虫、线虫或其食物供应链、栖息地、繁殖地以及其它场所与农药有效量的权利要求1或2所定义的组合物接触。
4.一种保护植物繁殖材料的方法,其特征在于,该方法包括使植物繁殖材料与农药有效量的权利要求1或2所定义的组合物接触,以免所述材料被昆虫或线虫危害。
5.权利要求1或2所述的组合物在对抗昆虫或线虫中的用途。
6.一种农药组合物,其特征在于,包含固体或液体载体以及权利要求1或2所述的组合物。
7.权利要求1或2所述的组合物在防治植物虫害中的用途,所述虫害为昆虫或线虫。
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CN116806836B (zh) * | 2023-08-30 | 2023-11-21 | 山东科大创业生物有限公司 | 一种杀线虫剂组合物、杀线虫制剂及其应用 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102077835A (zh) * | 2011-03-10 | 2011-06-01 | 陕西汤普森生物科技有限公司 | 一种含有氟啶虫胺腈的杀虫组合物 |
CN111436442A (zh) * | 2019-01-17 | 2020-07-24 | 海利尔药业集团股份有限公司 | 一种含氟氯虫双酰胺与新烟碱类杀虫剂的组合物 |
CN113875758A (zh) * | 2020-07-01 | 2022-01-04 | 山东省联合农药工业有限公司 | 一种含有三氟杀线酯和杀螨剂的复配组合物及其制备方法和用途 |
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Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102077835A (zh) * | 2011-03-10 | 2011-06-01 | 陕西汤普森生物科技有限公司 | 一种含有氟啶虫胺腈的杀虫组合物 |
CN111436442A (zh) * | 2019-01-17 | 2020-07-24 | 海利尔药业集团股份有限公司 | 一种含氟氯虫双酰胺与新烟碱类杀虫剂的组合物 |
CN113875758A (zh) * | 2020-07-01 | 2022-01-04 | 山东省联合农药工业有限公司 | 一种含有三氟杀线酯和杀螨剂的复配组合物及其制备方法和用途 |
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