CN107072209A - 除草组合物 - Google Patents
除草组合物 Download PDFInfo
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- CN107072209A CN107072209A CN201580057287.4A CN201580057287A CN107072209A CN 107072209 A CN107072209 A CN 107072209A CN 201580057287 A CN201580057287 A CN 201580057287A CN 107072209 A CN107072209 A CN 107072209A
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- compound
- test example
- salt
- sodium
- herbicidal
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- 150000003839 salts Chemical class 0.000 claims abstract description 26
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- 238000000034 method Methods 0.000 claims abstract description 24
- YUVKUEAFAVKILW-UHFFFAOYSA-N 2-(4-{[5-(trifluoromethyl)pyridin-2-yl]oxy}phenoxy)propanoic acid Chemical compound C1=CC(OC(C)C(O)=O)=CC=C1OC1=CC=C(C(F)(F)F)C=N1 YUVKUEAFAVKILW-UHFFFAOYSA-N 0.000 claims abstract description 23
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- SIVJKMBJGCUUNS-UHFFFAOYSA-M potassium;2-(2,4-dichlorophenoxy)propanoate Chemical compound [K+].[O-]C(=O)C(C)OC1=CC=C(Cl)C=C1Cl SIVJKMBJGCUUNS-UHFFFAOYSA-M 0.000 description 1
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- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- ABOOPXYCKNFDNJ-SNVBAGLBSA-N quizalofop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-SNVBAGLBSA-N 0.000 description 1
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- XWAFIZUTHLRWBE-NUBCRITNSA-M sodium;(2r)-2-(2,4-dichlorophenoxy)propanoate Chemical compound [Na+].[O-]C(=O)[C@@H](C)OC1=CC=C(Cl)C=C1Cl XWAFIZUTHLRWBE-NUBCRITNSA-M 0.000 description 1
- RFOHRSIAXQACDB-UHFFFAOYSA-M sodium;2-(2,4-dichlorophenoxy)acetate Chemical compound [Na+].[O-]C(=O)COC1=CC=C(Cl)C=C1Cl RFOHRSIAXQACDB-UHFFFAOYSA-M 0.000 description 1
- DHJHUXNTNSRSEX-UHFFFAOYSA-M sodium;2-(4-chloro-2-methylphenoxy)propanoate Chemical compound [Na+].[O-]C(=O)C(C)OC1=CC=C(Cl)C=C1C DHJHUXNTNSRSEX-UHFFFAOYSA-M 0.000 description 1
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- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
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- IUQAXCIUEPFPSF-UHFFFAOYSA-N tembotrione Chemical compound ClC1=C(COCC(F)(F)F)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O IUQAXCIUEPFPSF-UHFFFAOYSA-N 0.000 description 1
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- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
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- GYICYQJEVCIYJY-UHFFFAOYSA-N thiophen-1-ylidenemethanone Chemical compound O=C=S1C=CC=C1 GYICYQJEVCIYJY-UHFFFAOYSA-N 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 210000003813 thumb Anatomy 0.000 description 1
- KJAMZCVTJDTESW-UHFFFAOYSA-N tiracizine Chemical compound C1CC2=CC=CC=C2N(C(=O)CN(C)C)C2=CC(NC(=O)OCC)=CC=C21 KJAMZCVTJDTESW-UHFFFAOYSA-N 0.000 description 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 description 1
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
- 230000014616 translation Effects 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
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Classifications
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- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
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- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
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- 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
- A01N37/18—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof
- A01N37/22—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 the group —CO—N<, e.g. carboxylic acid amides or imides; Thio analogues thereof the nitrogen atom being directly attached to an aromatic ring system, e.g. anilides
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- 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
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/66—1,3,5-Triazines, not hydrogenated and not substituted at the ring nitrogen atoms
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- A01N43/70—Diamino—1,3,5—triazines with only one oxygen, sulfur or halogen atom or only one cyano, thiocyano (—SCN), cyanato (—OCN) or azido (—N3) group directly attached to a ring carbon atom
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- A—HUMAN NECESSITIES
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- 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
- A01N43/80—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 1,2
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- A—HUMAN NECESSITIES
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- 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
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- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring
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- A—HUMAN NECESSITIES
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- 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
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- A—HUMAN NECESSITIES
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- 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
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/36—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< directly attached to at least one heterocyclic ring; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
本发明提供一种高活性的除草组合物,所述除草组合物以协同除草效果防除不期望的植物。本发明提供含有(A)溴谷隆或其盐、和(B)选自氯苯胺灵、S‑异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、碘苯腈、二甲戊灵、氟乐灵、苄草丹、禾草丹和茚草酮中的至少1种的除草性化合物、其烷基酯或其盐的除草组合物、以及使用了所述组合物的除草方法。
Description
技术领域
本发明涉及除草组合物及不期望的植物的防除方法。
背景技术
专利文献1中记载了包含溴谷隆的式(I)的尿素衍生物与其他除草剂的组合物。专利文献2中记载了派罗克杀草砜与其他除草剂的组合物。专利文献3中记载了含有啶嘧磺隆或其盐、和选自丁噻隆、敌草隆及溴谷隆中的至少1种的除草性化合物或其盐的除草组合物。
然而,在专利文献1、专利文献2及专利文献3中关于将(A)溴谷隆、与(B)选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、碘苯腈、二甲戊灵、氟乐灵、苄草丹、禾草丹和茚草酮中的至少1种的除草性化合物、其烷基酯或其盐组合没有具体记载。另外,在将它们组合的情况下,发挥协同除草效果尚未为人所知。
现有技术文献
专利文献
专利文献1:欧洲专利申请公开第163598号说明书
专利文献2:国际公开第2009/115420号
专利文献3:国际公开第2011/158843号
发明内容
发明所要解决的课题
现在,开发并使用了大量的除草组合物,但对于防除以作为防除的对象的杂草为代表的不期望的植物而言,有时不一定是充分的,期望出现高活性的除草组合物。
本发明的目的在于提供以低药量对不期望的杂草具有高的除草效果、并且具有协同除草效果的除草组合物。
用于解决课题的手段
本发明人等反复进行了各种研究,发现通过组合特定的化合物可获得高活性的除草组合物,从而完成了本发明。
即,本发明涉及一种除草组合物,其含有(A)溴谷隆或其盐(以下,简称为化合物A)和(B)选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、碘苯腈、二甲戊灵、氟乐灵、苄草丹、禾草丹和茚草酮中的至少1种的除草性化合物、其烷基酯或其盐(以下,简称为化合物B)作为有效成分。另外,本发明涉及防除不期望的植物或抑制它们生长的方法,将除草有效量的化合物A、和除草有效量的化合物B施用至不期望的植物或它们生长的场所。
发明的效果
通过本发明,可提供对不期望的植物为高活性且具有协同除草效果、并且对植物具有高安全性的除草组合物、及防除或抑制生长的方法。
在组合有2种有效成分的情况下的除草活性比该2种有效成分各自的除草活性的单纯合计(可期待的活性)大的情况下,将其称为协同作用。通过2种有效成分的组合而可期待的活性可以如下计算(参照Colby S.R.,“Weed”15卷,20~22页,1967年)。
E=α+β-(α×β÷100)
α;将除草剂X以xg/ha的量进行处理时的生长抑制率
β;将除草剂Y以yg/ha的量进行处理时的生长抑制率
E;将除草剂X以xg/ha的量和将除草剂Y以yg/ha的量进行处理时可期待的生长抑制率
即,在实际的生长抑制率(实测值)大于上述计算得到的生长抑制率(计算值)的情况下,可以说通过组合得到的活性显示协同作用。在通过上述式计算的情况下,本发明的除草组合物显示协同作用。
具体实施方式
作为化合物A的溴谷隆(通用名,metobromuron)是3-(4-溴苯基)-1-甲氧基-1-甲基脲。
以下详细说明化合物B。
氯苯胺灵(通用名,chlorpropham)是3-氯苯氨基甲酸异丙酯。
S-异丙甲草胺(通用名,S-metolachlor)是2-氯-N-(6-乙基邻甲苯基)-N-[(1S)-2-甲氧基-1-甲基乙基]乙酰胺。
氟噻草胺(通用名,flufenacet)是4’-氟-N-异丙基-2-[5-(三氟甲基)-1,3,4-噻二唑-2-基氧基]乙酰苯胺。
派罗克杀草砜(通用名,pyroxasulfone)是3-[5-(二氟甲氧基)-1-甲基-3-(三氟甲基)吡唑-4-基甲基磺酰基]-4,5-二氢-5,5-二甲基-1,2-噁唑。
烟嘧磺隆(通用名,nicosulfuron)是2-[(4,6-二甲氧基嘧啶-2-基氨基甲酰)氨基磺酰基]-N,N-二甲基烟酰胺。
精吡氟禾草灵(通用名,fluazifop-P-butyl)是(R)-2-[4-[5-(三氟甲基)-2-吡啶基氧基]苯氧基]丙酸丁酯。
扑草净(通用名,prometryn)是N2,N4-二异丙基-6-甲基硫基-1,3,5-三嗪-2,4-二胺。
碘苯腈(通用名,ioxynil)是4-羟基-3,5-二碘苯甲腈,作为其烷基酯,可举出碘苯腈辛酸酯(ioxynil-octanoate)等。
二甲戊灵(通用名,pendimethalin)是N-(1-乙基丙基)-2,6-二硝基-3,4-二甲苯胺。
氟乐灵(通用名,trifluralin)是α,α,α-三氟-2,6-二硝基-N,N-二丙基-对甲苯胺。
苄草丹(通用名,prosulfocarb)是S-苄基二丙基(硫代氨基甲酸酯)。
禾草丹(通用名,thiobencarb)是S-4-氯苄基二乙基(硫代氨基甲酸酯)。
茚草酮(通用名,indanofan)是(RS)-2-[2-(3-氯苯基)-2,3-环氧基丙基]-2-乙基茚满-1,3-二酮。
对于化合物A或化合物B而言,除了上述物质之外,有时形成烷基酯、盐,有时存在异构体,只要是在农业上被允许的物质,均包含于本发明中。
化合物A与化合物B的混合比率需要根据制剂形态、气象条件、不期望的植物的种类、生长状况等适当调整,不能一概地确定,例如,以重量比计为200:1~1:40,优选为60:1~1:25,更优选为50:1~1:6。另外,将化合物A与化合物B的更详细的混用比率列举于第1表。
【表1】
第1表
对于化合物A和化合物B的除草有效量而言,需要根据化合物A与化合物B的混合比率、制剂形态、气象条件、不期望的植物的种类、生长状况等适当调整,不能一概确定,例如,化合物A为100~4000g/ha,化合物B为20~4000g/ha,优选的是,化合物A为60~1500g/ha,化合物B为25~1500g/ha。
本发明的除草组合物的施用可以为对不期望的植物施用或对它们生长的场所施用中的任一种。此外,可以在不期望的植物产生前后任何时期施用。而且可以选择土壤处理、茎叶处理、灌水处理、蓄水处理那样的各种撒布形态,能够应用于旱田、果树园、水田等农耕地、或田埂、休耕田、运动场、高尔夫球场、空地、森林、工场地皮、线路旁边、道路旁边等非农耕地。
本发明的除草组合物可以防除一年生杂草、多年生杂草等宽范围的不期望的植物。具体而言,可举出例如无刺鳞水蜈蚣(green kyllinga(Kyllinga brevifoliaRottb.var.leiolepis))、莎草属杂草(sedge(Cyperus spp.))〔作为莎草属杂草,可举出例如香附子(purple nutsedge(Cyperus rotundus L.))、异型莎草(smallflower umbrellasedge(Cyperus difformis L.))、油莎豆(yellow nutsedge(Cyperus esculentus L.))、具芒碎米莎草(amur cyperus(Cyperus microiria Steud.))等〕那样的莎草科杂草(cyperaceae);稗(barnyardgrass(Echinochloa crus-galli L.、Echinochloa oryzicolavasing.))、紫穗稗(Japanese millet(Echinochloa utilis Ohwi et Yabuno))、马唐属杂草(crabgrass(Digitaria spp.))〔作为马唐属杂草,可举出例如升马唐(summergrass(Digitaria ciliaris(Retz.)Koel)、马唐(large crabgrass(Digitaria sanguinalisL.))、紫马唐(violet crabgrass(Digitaria violascens Link))、Digitaria horizontalis Willd.等〕、狗尾草(green foxtail(Setaria viridisL.))、大狗尾草(giant foxtail(Setaria faberi Herrm.))、牛筋草(goosegrass(Eleusine indicaL.))、石茅(johnsongrass(Sorghum halepense(L.)Pers.))、狗牙根(bermudagrass(Cynodon dactylon(L.)Pers.))、野燕麦(wild oat(Avena fatua L.))、早熟禾(annualbluegrass(Poa annuaL.))、黍属草(panic grass(Ppanicum spp.))〔作为黍属杂草,可举出例如大黍(guinea grass(Panicum maximum Jacq.))、洋野黍(fall panicum(Panicum dichotomiflorum(L.)Michx.))等〕、臂形草属草(signal grass(Brachiaria spp.))〔作为臂形草属草,可举出例如车前状臂形草(plantain signal grass(Brachiaria plantaginea(LINK)Hitchc.))、伏生臂形草(palisade signal grass(Brachiaria decumbens Stapf))、mauritius signal grass(Brachiaria mutica(Forssk.)Stapf)等〕、雀稗属(paspalum(Paspalum spp.))、筒轴茅(itchgrass(Rottboellia cochinchinensis(LOUR.)W.D.CLAYTON))、蒺藜草(southern sandbur(Cenchrus echinatus L.))、高粱(shattercane(Sorghum bicolor(L.)Moench.))、多花黑麦草(italian ryegrass(Lolium multiflorum Lam.))那样的禾本科杂草(gramineae);阿拉伯婆婆纳(persian speedwell(Veronica persicaPoir.))、直立婆婆纳(corn speedwell(Veronica arvensis L.))那样的玄参科杂草(scrophulariaceae);鬼针草属杂草(beggar ticks(Bidens spp.))〔作为鬼针草属杂草,可举出例如鬼针草(hairy beggarticks(Bidens pilosa L.))、大狼杷草(devils berggarticks(Bidens frondosa L.))、金盏银盘(Bidens biternata(Lour.)Merr.et Sherff)、beggarticks(Bidens subalternansDC.)等〕、香丝草(hairy fleabane(Conyza bonariensis(L.)Cronq.))、加拿大飞蓬(horseweed(Erigeron canadensisL.))、药用蒲公英(dandelion(Taraxacum officinale Weber))、欧洲苍耳(commoncocklebur(Xanthium strumarium L.))那样的菊科杂草(compositae);猪屎豆属杂草(rattlepod or rattlebox(Crotalaria spp.))〔作为猪屎豆属杂草,可举出例如菽麻(sunn-hemp(Crotalaria juncea L.))等〕、田菁属杂草(poison bean(Sesbania spp.))〔作为田菁属杂草,可举出例如rostrate sesbania(Sesbania rostrata Bremek.&Oberm.)、田菁(sesbania pea(Sesbania cannabina(Retz.)Pers.))等〕、白车轴草(whiteclover(Trifolium repens L.))那样的豆科杂草(leguminosae);球序卷耳(stickychickweed(Cerastium glomeratum Thuill.))、繁缕(common chickweed(Stellaria media L.))那样的石竹科杂草(caryophyllaceae);飞扬草(garden spurge(Euphorbia hirta L.))、铁苋菜(threeseeded copperleaf(Acalypha australis L.))、白苞猩猩草(fireplant(Euphorbia heterophylla L.))那样的大戟科杂草(euphorbiaceae);车前(asiatic plantain(Plantago asiatica L.))那样的车前草科杂草(plantaginaceae);醋浆草(creeping woodsorrel(Oxalis corniculata L.))那样的醋浆草科杂草(oxalidaceae);天胡荽(lawn pennywort(Hydrocotyle sibthorpioides Lam.))那样的伞形科杂草(apiaceae);东北堇菜(violet(Viola mandshurica W.Becker))那样的堇菜科杂草(violaceae);庭菖蒲(blue-eyedgrass(Sisyrinchium rosulatum Bicknell))那样的鸢尾科杂草(iridaceae);野老鹳草(carolina geranium(Geranium carolinianum L.))那样的牻牛儿苗科杂草(geraniaceae);紫花野芝麻(purple deadnettle(Lamium purpureumL.))、宝盖草(henbit(Lamium amplexicaule L.))那样的唇形科杂草(labiatae);苘麻(velvetleaf(Abutilon theophrasti MEDIC.))、刺黄花稔(prickly sida (Sida spinosaL.))那样的锦葵科杂草(malvaceae);牵牛(ivy-leaved morningglory(Ipomoea hederacea(L.)Jacq.))、圆叶牵牛(common morningglory(Ipomoea purpurea ROTH))、茑萝松(cypressvine morningglory(Ipomoea quamoclit L.))、Ipomoea grandifolia(DAMMERMANN)O'DONNELL、hairy merremia(Merremia aegyptia(L.)URBAN)、田旋花(fieldBindweed(Convolvulus arvensis L.))那样的旋花科杂草(convolvulaceae);藜(commonlambsquarters(Chenopodium album L.))那样的藜科杂草(chenopodiaceae);马齿苋(common purslane(Portulaca oleracea L.))那样的马齿苋科杂草(portulacaceae);苋属杂草(pigweed(Amaranthus spp.))〔作为苋属杂草,可举出例如北美苋(prostratepigweed(Amaranthus blitoides S.Wats.))、凹头苋(livid amaranth(Amaranthus lividus L.)、繁穗苋(purple amaranth(Amaranthus blitum L.))、绿穗苋(smoothpigweed(Amaranthus hybridus L.)、Amaranthus patulus Bertol.)、鲍威尔苋(powellamaranth(Amaranthus powellii S.Wats.))、皱果苋(slender amaranth(Amaranthus viridis L.))、长芒苋(palmer amaranth(Amaranthus palmeri S.Wats.))、反枝苋(redroot pigweed(Amaranthus retroflexus L.))、糙果苋(tall waterhemp(Amaranthus tuberculatus(Moq.)Sauer.))、common waterhemp(Amaranthus tamariscinus Nutt.)、刺苋(thorny amaranth(Amaranthus spinosus L.))、ataco(Amaranthus quitensis Kunth.)、西部苋(Amaranthus rudis Sauer)等〕那样的苋科杂草(amaranthaceae);龙葵(black nightshade(Solanum nigrum L.))那样的茄科杂草(solanaceae);酸模叶蓼(spotted knotweed(Polygonum lapathifolium L.))、酸模叶蓼(green smartweed(Polygonum scabrumMOENCH))、犬蓼(Oriental lady's thumb(Persicaria longiseta))、尼泊尔蓼(Nepalese Smartweed(Persicaria nepalensis(Meisn.)H.Gross))那样的蓼科杂草(polygonaceae);弯曲碎米荠(flexuous bittercress(Cardamine flexuosa WITH.))那样的十字花科杂草(cruciferae);刺果瓜(burcucumber(Sicyos angulatus L.))那样的葫芦科杂草(cucurbitaceae);鸭跖草(common dayflower(Commelina communis L.))那样的鸭跖草科杂草(commelinaceae);皱果蛇莓(mockstrawberry(Duchesnea chrysantha(Zoll.et Mor.)Miq.))那样的蔷薇科杂草(rosaceae);种棱粟米草(carpetweed(Mollugo verticillata L.))那样的栗米草科杂草(molluginacea);拉拉藤(false cleavers(Galium spurium var.echinospermon(Wallr.)Hayek))、原拉拉藤(stickywilly(Galium aparine L.))那样的茜草科杂草(rubiaceae);等等。
本发明的除草组合物在实用场合下是非常有用的。例如,有以下那样的情况。
(1)本发明的除草组合物发挥显著的协同效果,即使化合物A和化合物B双方的施用量为少量,也发挥良好的除草效果,因此对周边环境的影响被抑制。
(2)有时可以提供与将化合物A、和化合物B分别单独施用的情况相比,除草效果的持续性长,即,具有长期残效性的除草组合物。
(3)有时可以提供与将化合物A、和化合物B分别单独施用的情况相比,对禾本科草种和阔叶草种这两者显示高的效果的广谱的除草组合物。
(4)由于为化合物A和化合物B的作用性不同的组合,因此有时抑制除草剂抵抗性杂草、低敏感性杂草的出现。
(5)与将化合物A、和化合物B分别单独施用的情况相比,有时对有用作物的安全性提高。
本发明的除草组合物可以混用以下所列举的公知除草性化合物(通用名等),由此有时可以将适用草种的范围、药剂处理的时期、除草活性等向更优选的方向改良。特别是即使在没有记载的情况下,在这些化合物存在盐、烷基酯、水合物、不同晶形、各种结构异构体等的情况下,当然它们也包含在内。
(1)2,4-D、2,4-D丁氧基乙酯(2,4-D-butotyl)、2,4-D丁酯(2,4-D-butyl)、2,4-D二甲基铵(2,4-D-dimethylammonimum)、2,4-D二醇胺(2,4-D-diolamine)、2,4-D乙酯(2,4-D-ethyl)、2,4-D-2-乙基己酯(2,4-D-2-ethylhexyl)、2,4-D异丁酯(2,4-D-isobutyl)、2,4-D异辛酯(2,4-D-isoctyl)、2,4-D异丙酯(2,4-D-isopropyl)、2,4-D异丙基铵(2,4-D-isopropylammonium)、2,4-D钠(2,4-D-sodium)、2,4-D异丙醇铵(2,4-D-isopropanolammonium)、2,4-D三乙醇胺(2,4-D-trolamine)、2,4-DB、2,4-DB丁酯(2,4-DB-butyl)、2,4-DB二甲基铵(2,4-DB-dimethylammonium)、2,4-DB异辛酯(2,4-DB-isoctyl)、2,4-DB钾(2,4-DB-potassium)、2,4-DB钠(2,4-DB-sodium)、2,4-滴丙酸(dichlorprop)、2,4-滴丙酸丁氧基乙酯(dichlorprop-butotyl)、2,4-滴丙酸二甲基铵(dichlorprop-dimethylammonium)、2,4-滴丙酸异辛酯(dichlorprop-isoctyl)、2,4-滴丙酸钾(dichlorprop-potassium)、高2,4-滴丙酸(dichlorprop-P)、高2,4-滴丙酸二甲基铵(dichlorprop-P-dimethylammonium)、高2,4-滴丙酸钾(dichlorprop-P-potassium)、高2,4-滴丙酸钠(dichlorprop-P-sodium)、MCPA、MCPA丁氧基乙酯(MCPA-butotyl)、MCPA二甲基铵(MCPA-dimethylammonium)、MCPA-2-乙基己酯(MCPA-2-ethylhexyl)、MCPA钾(MCPA-potassium)、MCPA钠(MCPA-sodium)、MCPA乙硫酯(MCPA-thioethyl)、MCPB、MCPB乙酯(MCPB-ethyl)、MCPB钠(MCPB-sodium)、2甲4氯丙酸(mecoprop)、2甲4氯丙酸丁氧基乙酯(mecoprop-butotyl)、2甲4氯丙酸钠(mecoprop-sodium)、高2甲4氯丙酸(mecoprop-P)、高2甲4氯丙酸丁氧基乙酯(mecoprop-P-butotyl)、高2甲4氯丙酸二甲基铵(mecoprop-P-dimethylammonium)、高2甲4氯丙酸2-乙基己酯(mecoprop-P-2-ethylhexyl)、高2甲4氯丙酸钾(mecoprop-P-potassium)、萘丙胺(naproanilide)、氯甲酰草胺(clomeprop)那样的苯氧基系化合物;2,3,6-TBA、麦草畏(dicamba)、麦草畏丁氧基乙酯(dicamba-butotyl)、麦草畏二甘醇胺(dicamba-diglycolamine)、麦草畏二甲基铵(dicamba-dimethylammonium)、麦草畏二醇胺(dicamba-diolamine)、麦草畏异丙基铵(dicamba-isopropylammonium)、麦草畏钾(dicamba-potassium)、麦草畏钠(dicamba-sodium)、氨氯吡啶酸(picloram)、氨氯吡啶酸二甲基铵(picloram-dimethylammonium)、氨氯吡啶酸异辛酯(picloram-isoctyl)、氨氯吡啶酸钾(picloram-potassium)、氨氯吡啶酸三异丙醇铵(picloram-triisopropanolammonium)、氨氯吡啶酸三异丙基铵(picloram-triisopropylammonium)、氨氯吡啶酸三乙醇胺(picloram-trolamine)、绿草定(triclopyr)、绿草定丁氧基乙酯(triclopyr-butotyl)、绿草定三乙基铵(triclopyr-triethylammonium)、二氯吡啶酸(clopyralid)、二氯吡啶酸醇胺(clopyralid-olamine)、二氯吡啶酸钾(clopyralid-potassium)、二氯吡啶酸三异丙醇铵(clopyralid-triisopropanolammonium)、氯氨吡啶酸(aminopyralid)、环丙嘧啶酸(aminocyclopyrachlor)、halauxifen那样的芳香族羧酸系化合物;其它的萘草胺(naptalam)、萘草胺钠(naptalam-sodium)、草除灵(benazolin)、草除灵乙酯(benazolin-ethyl)、二氯喹啉酸(quinclorac)、氯甲喹啉酸(quinmerac)、氟吡草腙(diflufenzopyr)、氟吡草腙钠(diflufenzopyr-sodium)、氯氟吡氧乙酸(fluroxypyr)、氯氟吡氧乙酸-2-丁氧基-1-甲基乙酯(fluroxypyr-2-butoxy-1-methylethyl)、氯氟吡氧乙酸异辛酯(fluroxypyr-meptyl)、整形醇(chlorflurenol)、整形醇甲酯(chlorflurenol-methyl)等那样的通过搅乱植物的激素作用而显示除草效力的化合物。
(2)绿麦隆(chlorotoluron)、敌草隆(diuron)、氟草隆(fluometuron)、利谷隆(linuron)、异丙隆(isoproturon)、吡喃隆(metobenzuron)、丁噻隆(tebuthiuron)、恶唑隆(dimefuron)、异恶隆(isouron)、特胺灵(karbutilate)、甲基苯噻隆(methabenzthiazuron)、甲氧隆(metoxuron)、绿谷隆(monolinuron)、草不隆(neburon)、环草隆(siduron)、特丁通(terbumeton)、草达津(trietazine)那样的脲系化合物;西玛津(simazine)、莠去津(atrazine)、阿特拉通(atratone)、西草净(simetryn)、扑草净(prometryn)、异戊乙净(dimethametryn)、环嗪酮(hexazinone)、嗪草酮(metribuzin)、特丁津(terbuthylazine)、氰草津(cyanazine)、莠灭净(ametryn)、cybutryne、特丁净(terbutryn)、扑灭津(propazine)、苯嗪草酮(metamitron)、扑灭通(prometon)那样的三嗪系化合物;除草定(bromacil)、除草定锂(bromacyl-lithium)、环草定(lenacil)、特草定(terbacil)那样的尿嘧啶系化合物;敌稗(propanil)、环酰草胺(cypromid)那样的酰苯胺系化合物;灭草灵(swep)、甜菜安(desmedipham)、甜菜宁(phenmedipham)那样的氨基甲酸酯系化合物;溴苯腈(bromoxynil)、辛酰溴苯腈(bromoxynil-octanoate)、庚酰溴苯腈(bromoxynil-heptanoate)、碘苯腈(ioxynil)、辛酰碘苯腈(ioxynil-octanoate)、碘苯腈钾(ioxynil-potassium)、碘苯腈钠(ioxynil-sodium)那样的羟基苄腈系化合物;其它的哒草特(pyridate)、灭草松(bentazone)、灭草松钠(bentazone-sodium)、氨唑草酮(amicarbazone)、灭草唑(methazole)、甲氯酰草胺(pentanochlor)、甜菜宁(phenmedipham)等那样的通过阻碍植物的光合作用来显示除草效力的化合物。
(3)其本身在植物体中成为游离自由基,使活性氧生成而显示速效的除草效力的百草枯(paraquat)、敌草快(diquat)那样的季铵盐系化合物。
(4)除草醚(nitrofen)、甲氧除草醚(chlomethoxyfen)、甲羧除草醚(bifenox)、三氟羧草醚(acifluorfen)、三氟羧草醚钠(acifluorfen-sodium)、氟磺胺草醚(fomesafen)、氟磺胺草醚钠(fomesafen-sodium)、乙氧氟草醚(oxyfluorfen)、乳氟禾草灵(lactofen)、苯草醚(aclonifen)、氯氟草醚(ethoxyfen-ethyl)、乙羧氟草醚(fluoroglycofen-ethyl)、三氟硝草醚(fluoroglycofen)那样的二苯基醚系化合物;氯酞亚胺(chlorphthalim)、丙炔氟草胺(flumioxazin)、氟烯草酸(flumiclorac)、氟胺草酯(flumiclorac-pentyl)、吲哚酮草酯(cinidon-ethyl)、嗪草酸甲酯(fluthiacet-methyl)那样的环状酰亚胺系化合物;其它的丙炔恶草酮(oxadiargyl)、恶草灵(oxadiazon)、甲磺草胺(sulfentrazone)、唑酮草酯(carfentrazone-ethyl)、噻二唑草胺(thidiazimin)、环戊恶草酮(pentoxazone)、唑啶草酮(azafenidin)、氟溴唑酯(isopropazole)、吡草醚(pyraflufen-ethyl)、双苯嘧草酮(benzfendizone)、氟丙嘧草酯(butafenacil)、苯嘧磺草胺(saflufenacil)、异丙吡草酯(fluazolate)、氟唑草胺(profluazol)、氟哒嗪草酯(flufenpyr-ethyl)、bencarbazone、thiafenacil、双唑草腈(pyrachlonil)等那样的阻碍植物的叶绿素生物合成,在植物体中使光敏化过氧化物异常蓄积,从而显示除草效力的化合物。
(5)氟草敏(norflurazon)、氯草敏(chloridazon)、二甲哒草伏(metflurazon)那样的四氢哒嗪酮系化合物;吡唑特(pyrazolynate)、苄草唑(pyrazoxyfen)、吡草酮(benzofenap)、苯吡唑草酮(topramezone)、磺酰草吡唑(pyrasulfotole)那样的吡唑系化合物;其它的杀草强(amitrole)、氟啶草酮(fluridone)、呋草酮(flurtamone)、吡氟酰草胺(diflufenican)、苯草酮(methoxyphenone)、异恶草松(clomazone)、磺草酮(sulcotrione)、甲基磺草酮(mesotrione)、环磺酮(tembotrione)、特糠酯酮(tefuryltrione)、KUH-110、SW-065、异唑草酮(isoxaflutole)、野燕枯(difenzoquat)、野燕枯甲硫酸盐(difenzoquat-metilsulfate)、异氯草酮(isoxachlortole)、双环磺草酮(benzobicyclon)、双环吡喃酮(bicyclopyron)、氟吡草胺(picolinafen)、氟丁酰草胺(beflubutamid)等那样的阻碍类胡萝卜素等植物的色素生物合成,显示以泛白作用为特征的除草效力的化合物。
(6)禾草灵(diclofop-methyl)、禾草灵脱甲基酸(diclofop)、pyriphenop-sodium、吡氟禾草灵(fluazifop-butyl)、吡氟禾草灵脱丁基酸(fluazifop)、精吡氟禾草灵脱丁基酸(fluazifop-P)、精吡氟禾草灵(fluazifop-P-butyl)、氟吡甲禾灵(haloxyfop-methyl)、氟吡甲禾灵脱甲基酸(haloxyfop)、氟吡乙禾灵(haloxyfop-etotyl)、精氟吡甲禾灵脱甲基酸(haloxyfop-P)、精氟吡甲禾灵(haloxyfop-P-methyl)、喹禾灵(quizalofop-ethyl)、精喹禾灵脱乙基酸(quizalofop-P)、精喹禾灵(quizalofop-P-ethyl)、喹禾糠酯(quizalofop-P-tefuryl)、氰氟草酯(cyhalofop-butyl)、恶唑禾草灵(fenoxaprop-ethyl)、精恶唑禾草灵脱乙基酸(fenoxaprop-P)、精恶唑禾草灵(fenoxaprop-P-ethyl)、metamifop-propyl、恶唑酰草胺(metamifop)、炔草酯(clodinafop-propargyl)、炔草酸(clodinafop)、恶草酸(propaquizafop)那样的芳基氧基苯氧基丙酸系化合物;禾草灭钠(alloxydim-sodium)、禾草灭(alloxydim)、烯草酮(clethodim)、烯禾啶(sethoxydim)、三甲苯草酮(tralkoxydim)、丁苯草酮(butroxydim)、吡喃草酮(tepraloxydim)、环苯草酮(profoxydim)、噻草酮(cycloxydim)那样的环己烷二酮系化合物;唑啉草酯(pinoxaden)那样的苯基吡唑啉系化合物;等那样的阻碍脂肪酸的生物合成,对植物显示除草效力的化合物。
(7)氯嘧磺隆(chlorimuron-ethyl)、氯嘧磺隆脱乙基酸(chlorimuron)、甲嘧磺隆(sulfometuron-methyl)、甲嘧磺隆脱甲基酸(sulfometuron)、氟嘧磺隆(primisulfuron-methyl)、氟嘧磺隆脱甲基酸(primisulfuron)、苄嘧磺隆(bensulfuron-methyl)、苄嘧磺隆脱甲基酸(bensulfuron)、氯磺隆(chlorsulfuron)、甲磺隆(metsulfuron-methyl)、甲磺隆脱甲基酸(metsulfuron)、醚磺隆(cinosulfuron)、吡嘧磺隆(pyrazosulfuron-ethyl)、吡嘧磺隆脱乙基酸(pyrazosulfuron)、啶嘧磺隆(flazasulfuron)、砜嘧磺隆(rimsulfuron)、烟嘧磺隆(nicosulfuron)、唑吡嘧磺隆(imazosulfuron)、氟吡磺隆(flucetosulfuron)、环丙嘧磺隆(cyclosulfamuron)、氟磺隆(prosulfuron)、氟啶嘧磺隆(flupyrsulfuron-methyl-sodium)、氟啶嘧磺隆脱甲基酸(flupyrsulfuron)、氟胺磺隆(triflusulfuron-methyl)、氟胺磺隆脱甲基酸(triflusulfuron)、氯吡嘧磺隆(halosulfuron-methyl)、氯吡嘧磺隆脱甲基酸(halosulfuron)、噻吩磺隆(thifensulfuron-methyl)、噻吩磺隆脱甲基酸(thifensulfuron)、乙氧磺隆(ethoxysulfuron)、环氧嘧磺隆(oxasulfuron)、胺苯磺隆脱甲基酸(ethametsulfuron)、胺苯磺隆(ethametsulfuron-methyl)、碘甲磺隆脱甲基酸(iodosulfuron)、碘甲磺隆钠盐(iodosulfuron-methyl-sodium)、磺酰磺隆(sulfosulfuron)、醚苯磺隆(triasulfuron)、苯磺隆(tribenuron-methyl)、苯磺隆脱甲基酸(tribenuron)、三氟甲磺隆(tritosulfuron)、甲酰胺磺隆(foramsulfuron)、三氟啶磺隆(trifloxysulfuron)、三氟啶磺隆钠(trifloxysulfuron-sodium)、甲磺胺磺隆(mesosulfuron-methyl)、甲磺胺磺隆脱甲基酸(mesosulfuron)、嘧苯胺磺隆(orthosulfamuron)、酰嘧磺隆(amidosulfuron)、四唑嘧磺隆(azimsulfuron)、propyrisulfuron、双醚氯吡嘧磺隆(metazosulfuron)、甲硫嘧磺隆(methiopyrsulfuron)、monosulfuron-methyl、orsosulfuron那样的磺酰基脲化合物;唑嘧磺草胺(flumetsulam)、磺草唑胺(metosulam)、双氯磺草胺(diclosulam)、氯酯磺草胺(cloransulam-methyl)、双氟磺草胺(florasulam)、五氟磺草胺(penoxsulam)、啶磺草胺(pyroxsulam)那样的三唑并嘧啶磺酰胺系化合物;咪唑烟酸(imazapyr)、咪唑烟酸异丙基铵(imazapyr-isopropylammonium)、咪唑乙烟酸(imazethapyr)、咪唑乙烟酸铵(imazethapyr-ammonium)、咪唑喹啉酸(imazaquin)、咪唑喹啉酸铵(imazaquin-ammonium)、甲氧咪草烟(imazamox)、甲氧咪草烟铵(imazamox-ammonium)、咪草酸(imazamethabenz)、咪草酸甲酯(imazamethabenz-methyl)、甲基咪草烟(imazapic)那样的咪唑啉酮系化合物;嘧草硫醚(pyrithiobac-sodium)、双草醚(bispyribac-sodium)、嘧草醚(pyriminobac-methyl)、嘧啶肟草醚(pyribenzoxim)、环酯草醚(pyriftalid)、嘧啶硫蕃(pyrimisulfan)、氟酮磺草胺(triafamone)那样的嘧啶基水杨酸系化合物;氟酮磺隆(flucarbazone)、氟酮磺隆钠(flucarbazone-sodium)、丙苯磺隆钠(propoxycarbazone-sodium)、丙苯磺隆(propoxycarbazone)、噻酮磺隆(thiencarbazone-methyl)那样的磺酰氨基羰基三唑啉酮系化合物;其它的草甘膦(glyphosate)、草甘膦钠(glyphosate-sodium)、草甘膦钾(glyphosate-potassium)、草甘膦铵(glyphosate-ammonium)、草甘膦二铵(glyphosate-diammonium)、草甘膦异丙基铵(glyphosate-isopropylammonium)、草硫膦(glyphosate-trimesium)、增甘膦钠(glyphosate-sesquisodium)、草铵膦(glufosinate)、草铵膦铵(glufosinate-ammonium)、草铵膦-P(glufosinate-P)、草铵膦-P铵(glufosinate-P-ammonium)、草铵膦-P钠(glufosinate-P-sodium)、双丙氨酰膦(bilanafos)、双丙氨酰膦钠(bilanafos-sodium)、环庚草醚(cinmethylin)等那样的通过阻碍植物的氨基酸生物合成而显示除草效力的化合物。
(8)氟乐灵(trifluralin)、氨磺乐灵(oryzalin)、甲磺乐灵(nitralin)、二甲戊灵(pendimethalin)、乙丁烯氟灵(ethalfluralin)、乙丁氟灵(benfluralin)、氨氟乐灵(prodiamine)、仲丁灵(butralin)、氨氟灵(dinitramine)那样的二硝基苯胺系化合物;地散磷(bensulide)、敌草胺(napropamide)、炔苯酰草胺(propyzamide、拿草特(pronamide))那样的酰胺系化合物;甲基胺草磷(amiprofos-methyl)、抑草磷(butamifos)、莎稗磷(anilofos)、哌草磷(piperophos)那样的有机磷系化合物;苯胺灵(propham)、氯苯胺灵(chlorpropham)、燕麦灵(barban)、双酰草胺(carbetamide)那样的苯基氨基甲酸酯系化合物;杀草隆(daimuron)、苄草隆(cumyluron)、溴丁酰草胺(bromobutide)、甲基杀草隆(methyldymron)那样的枯基胺系化合物;其它的磺草灵(asulam)、磺草灵钠(asulam-sodium)、氟硫草定(dithiopyr)、噻草啶(thiazopyr)、氯酞酸甲酯(chlorthal-dimethyl)、氯酞酸(chlorthal)、双苯酰草胺(diphenamid)、高效麦草伏甲酯(flamprop-M-methyl)、高效麦草伏(flamprop-M)、高效麦草伏异丙酯(flamprop-M-isopropyl)等那样的通过阻碍植物的细胞有丝分裂而显示除草效力的化合物。
(9)甲草胺(alachlor)、吡唑草胺(metazachlor)、丁草胺(butachlor)、丙草胺(pretilachlor)、异丙甲草胺(metolachlor)、高效异丙甲草胺(S-metolachlor)、甲氧噻草胺(thenylchlor)、烯草胺(pethoxamid)、乙草胺(acetochlor)、毒草胺(propachlor)、二甲吩草胺(dimethenamid)、二甲吩草胺-P(dimethenamid-P)、异丙草胺(propisochlor)、二甲草胺(dimethachlor)那样的氯乙酰胺系化合物;禾草敌(molinate)、哌草丹(dimepiperate)、稗草丹(pyributicarb)、EPTC、丁草敌(butylate)、灭草敌(vernolate)、克草敌(pebulate)、环草敌(cycloate)、苄草丹(prosulfocarb)、戊草丹(esprocarb)、禾草丹(thiobencarb)、燕麦敌(diallate)、野麦畏(tri-allate)、坪草丹(orbencarb)那样的硫代氨基甲酸酯系化合物;其它的乙氧苯草胺(etobenzanid)、苯噻酰草胺(mefenacet)、氟噻草胺(flufenacet)、灭草环(tridiphane)、唑草胺(cafenstrole)、四唑酰草胺(fentrazamide)、嗪草酮(oxaziclomefone)、茚草酮(indanofan)、呋草黄(benfuresate)、派罗克杀草砜(pyroxasulfone)、fenoxasulfone、methiozolin、茅草枯(dalapon)、茅草枯钠(dalapon-sodium)、TCA钠(TCA-sodium)、三氯乙酸(trichloroaceticacid)等那样的通过阻碍植物的蛋白质生物合成或脂质生物合成而显示除草效力的化合物。
(10)敌草腈(dichlobenil)、三嗪氟草胺(triaziflam)、indaziflam、氟胺草唑(flupoxam)等那样的通过阻碍植物的纤维素生物合成而显示除草效力的化合物。
(11)MSMA、DSMA、CMA、内氧草素(endothall)、内氧草素二钾(endothall-dipotassium)、内氧草素钠(endothall-sodium)、内氧草素单(N,N-二甲基烷基铵)(endothall-mono(N,N-dimethylalkylammonium))、乙氧呋草黄(ethofumesate)、氯酸钠(sodium chlorate)、壬酸(pelargonic acid、壬酸(nonanoic acid))、杀木膦(fosamine)、杀木膦铵(fosamine-ammonium)、ipfencarbazone、丙烯醛(aclolein)、氨基磺酸铵(ammonium sulfamate)、硼砂(borax)、氯乙酸(chloroacetic acid)、氯乙酸钠(sodiumchloroacete)、氨腈(cyanamide)、甲基胂酸(methylarsonic acid)、二甲胂酸(dimethylarsinicacid)、二甲基砷酸钠(sodium dimethylarsinate)、特乐酚(dinoterb)、特乐酚铵(dinoterb-ammonium)、特乐酚二醇胺(dinoterb-diolamine)、特乐酯(dinoterb-acetate)、DNOC、硫酸亚铁(ferrous sulfate)、四氟丙酸(flupropanate)、四氟丙酸钠(flupropanate-sodium)、异草胺(isoxaben)、氟磺酰草胺(mefluidide)、氟磺酰草胺二醇胺(mefluidide-diolamine)、威百亩(metam)、威百亩铵(metam-ammonium)、威百亩钾(metam-potassium)、威百亩钠(metam-sodium)、异硫氰酸甲酯(methyl isothiocyanate)、五氯苯酚(pentachlorophenol)、五氯苯酚钠(sodium pentachlorophenoxide)、五氯苯酚月桂酸酯(pentachlorophenol laurate)、灭藻醌(quinoclamine)、硫酸(sulfuric acid)、脲硫酸盐(urea sulfate)等其它除草剂。
(12)田野黄单胞菌(Xanthomonas campestris)、Epicoccosirus nematosorus、Epicoccosirus nematosperus、尖角突脐孢菌(Exserohilum monoseras)、稗内胳螺抱菌(Drechsrela monoceras)等那样的通过寄生于植物而显示除草效力的化合物。
本发明的除草组合物中,可以将作为有效成分的化合物A和化合物B按照通常的农药的制剂方法与各种辅助剂配合,制剂调制成粉剂、粒剂、水分散性颗粒剂(WG)、可湿性粉剂(WP)、片剂、丸剂、胶囊剂(包含以水溶性膜包装的形态)、水性悬浮剂(SC)、油性悬浮剂、微乳制剂、悬乳制剂、水溶剂、乳剂(EC)、液剂、糊剂等各种形态,进行施用。只要适合于本发明的目的,就可以制成通常的该领域所使用的所有制剂形态。
在制剂调制时,可以将化合物A与化合物B一起混合来进行制剂调制,或可以将它们分别进行制剂调制,在施用时进行混合。
作为制剂所使用的辅助剂,可举出高岭石、绢云母、硅藻土、消石灰、碳酸钙、滑石、白炭墨、高岭土、膨润土、粘土、碳酸钠、碳酸氢钠、芒硝、沸石、淀粉那样的固形载体;水、甲苯、二甲苯、溶剂石脑油、二烷、二甲亚砜、N,N-二甲基甲酰胺、二甲基乙酰胺、N-甲基-2-吡咯烷酮、醇那样的溶剂;脂肪酸盐、苯甲酸盐、多元羧酸盐、烷基硫酸酯盐、烷基硫酸盐、烷基芳基硫酸盐、烷基二甘醇醚硫酸盐、醇硫酸酯盐、烷基磺酸盐、烷基芳基磺酸盐、芳基磺酸盐、木质素磺酸盐、烷基二苯基醚二磺酸盐、聚苯乙烯磺酸盐、烷基磷酸酯盐、烷基芳基磷酸盐、苯乙烯基芳基磷酸盐、聚氧乙烯烷基醚硫酸酯盐、聚氧乙烯烷基芳基醚硫酸盐、聚氧乙烯烷基芳基醚硫酸酯盐、聚氧乙烯烷基醚磷酸盐、聚氧乙烯烷基芳基磷酸酯盐、聚氧乙烯芳基醚磷酸酯盐、萘磺酸甲醛缩合物、烷基萘磺酸甲醛缩合物的盐那样的阴离子系的表面活性剂;失水山梨糖醇脂肪酸酯、甘油脂肪酸酯、脂肪酸聚甘油酯、脂肪酸醇聚二醇醚、乙炔二醇、炔属醇、氧化烯嵌段聚合物、聚氧乙烯烷基醚、聚氧乙烯烷基芳基醚、聚氧乙烯苯乙烯基芳基醚、聚氧乙烯二醇烷基醚、聚乙二醇、聚氧乙烯脂肪酸酯、聚氧乙烯失水山梨糖醇脂肪酸酯、聚氧乙烯甘油脂肪酸酯、聚氧乙烯固化蓖麻油、聚氧丙烯脂肪酸酯那样的非离子系的表面活性剂;橄榄油、木棉油、蓖麻油、棕榈油、山茶油、椰子油、芝麻油、玉米油、米糠油、花生油、棉籽油、豆油、菜籽油、亚麻仁油、桐油、液状石蜡那样的植物油、矿物油等。这些辅助剂的各成分只要不脱离本发明的目的,就可以适当选择1种或2种以上来使用。此外,除了上述辅助剂以外,也可以从该领域已知的辅助剂中适当选择并使用。还可以使用例如,增量剂、增稠剂、沉降防止剂、防冻剂、分散稳定剂、安全剂、防霉剂、发泡剂、崩解剂、粘合剂等通常所使用的各种辅助剂。本发明的除草组合物中的有效成分与各种辅助剂的配合比例以重量%比计为0.001:99.999~95:5,可以优选为0.005:99.995~90:10左右。
本发明的除草组合物的施用方法可以采用各种方法,可以根据施用场所、制剂形态、不期望的植物的种类、生长状况等各种条件来适当分别使用,可举出例如以下那样的方法。
1.直接施用将化合物A与化合物B一起混合、进行制剂调制而成的物质。
2.用水等稀释将化合物A与化合物B一起混合、进行制剂调制而成的物质至规定浓度,根据需要添加各种展着剂(表面活性剂、植物油、矿物油等)来施用。
3.将化合物A和化合物B分别进行制剂调制,将各自直接施用。
4.将化合物A和化合物B分别进行制剂调制,根据需要将各自用水等稀释至规定浓度,根据需要添加各种展着剂(表面活性剂、植物油、矿物油等),各自施用。
5.将对化合物A和化合物B分别进行制剂调制而成的物质在用水等稀释至规定浓度时进行混合,根据需要添加各种展着剂(表面活性剂、植物油、矿物油等)来施用。
以下记载本发明中的优选方式的一例,但本发明不限定解释于此。
(1)一种除草组合物,其含有(A)溴谷隆或其盐、和(B)选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、碘苯腈、二甲戊灵、氟乐灵、苄草丹、禾草丹和茚草酮中的至少1种的除草性化合物或其盐。
(2)根据前述(1)所述的除草组合物,其中,(A)与(B)的混合比率以重量比计为200:1~1:40。
(3)根据前述(1)或(2)所述的除草组合物,其中,(B)的除草性化合物为氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、碘苯腈、二甲戊灵或氟乐灵。
(4)根据前述(1)或(2)所述的除草组合物,其中,(B)的除草性化合物为氯苯胺灵、S-异丙甲草胺、氟噻草胺或派罗克杀草砜。
(5)根据前述(1)或(2)所述的除草组合物,其中,(B)的除草性化合物为氯苯胺灵、S-异丙甲草胺、烟嘧磺隆、精吡氟禾草灵、二甲戊灵或氟乐灵。
(6)一种防除不期望的植物或抑制它们生长的方法,将除草有效量的(A)溴谷隆或其盐、和除草有效量的(B)选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、碘苯腈、二甲戊灵、氟乐灵、苄草丹、禾草丹和茚草酮中的至少1种的除草性化合物或其盐施用至不期望的植物或它们生长的场所。
(7)根据前述(6)所述的方法,施用100~4000g/ha的(A)、20~4000g/ha的(B)。
(8)根据前述(6)或(7)所述的方法,其中,(B)的除草性化合物为氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、碘苯腈、二甲戊灵或氟乐灵。
(9)根据前述(6)或(7)所述的方法,其中,(B)的除草性化合物为氯苯胺灵、S-异丙甲草胺、氟噻草胺或派罗克杀草砜。
(10)根据前述(6)或(7)所述的方法,其中,(B)的除草性化合物为氯苯胺灵、S-异丙甲草胺、烟嘧磺隆、精吡氟禾草灵、二甲戊灵、氟乐灵。
(11)根据前述(1)所述的除草组合物,其中,(A)为溴谷隆或其盐,(B)为选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、二甲戊灵、氟乐灵、苄草丹、禾草丹及茚草酮中的至少1种的除草性化合物或其盐。
(12)根据前述(11)所述的除草组合物,其中,(A)与(B)的混合比率以重量比计为50:1~1:6。
(13)根据前述(6)的方法,其中,(A)为溴谷隆或其盐,(B)为选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、二甲戊灵、氟乐灵、苄草丹、禾草丹及茚草酮中的至少1种的除草性化合物或其盐。
(14)根据前述(13)所述的方法,其中,将(A)和(B)以50:1~1:6的重量比混合施用。
实施例
为了更详细地说明本发明,以下记载实施例,但本发明不限定解释于此。
试验例1
在播种了稗(barnyardgrass(Echinochloa crus-galli L.))的种子的大豆田地(每1个试验区1.8平方米)中,在大豆及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(商品名:メトブロムロン500SC(Metobromuron 500SC),Belchim Crop Protection公司制)及以氯苯胺灵为有效成分的EC剂(商品名:クロロIPC“石原”(KURORO IPC“ISHIHARA”),石原产业株式会社制)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第19天,用肉眼观察调查稗的生长状态,按照下述评价基准进行评价。将生长抑制率(%)〔实测值〕及通过Colby方法算出的生长抑制率(%)〔计算值〕示于第2表。
生长抑制率(%)=0(无处理区同等)~100(完全枯死)的抑草率(%)
【表2】
第2表
试验例2
在播种了酸模叶蓼(spotted knotweed(Polygonum lapathifolium L.))的种子的大豆田地(每1个试验区1.8平方米)中,在大豆及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以S-异丙甲草胺为有效成分的EC剂(商品名:DualGold,Syngenta公司制)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第50天,用肉眼观察调查酸模叶蓼的生长状态,与试验例1同样地进行评价。将结果示于第3表。
【表3】
第3表
试验例3
在大豆田地(每1个试验区8.4平方米)中,在大豆及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以S-异丙甲草胺为有效成分的EC剂(与前述试验例2相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第50天,用肉眼观察调查自然产生的尼泊尔蓼(NepaleseSmartweed(Persicaria nepalensis(Meisn.)H.Gross))的生长状态,与试验例1同样地进行评价。将结果示于第4表。
【表4】
第4表
试验例4
在大豆田地(每1个试验区8.4平方米)中,在大豆及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以氟乐灵为有效成分的EC剂(商品名:トレファノサイド乳剂(TOREFANOCIDE NYUZAI),Dow AgroScience公司制)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第50天,用肉眼观察调查自然产生的稗(barnyardgrass(Echinochloa crus-galli L.))的生长状态,与试验例1同样地进行评价。将结果示于第5表。
【表5】
第5表
试验例5
在小豆田地(每1个试验区9.6平方米)中,在小豆及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以精吡氟禾草灵为有效成分的EC剂(商品名:ワンサイドP乳剂(ONECIDE P NYUZAI),石原产业株式会社制)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第39天,用肉眼观察调查自然产生的稗(barnyardgrass(Echinochloa crus-galli L.))的生长状态,与试验例1同样地进行评价。将结果示于第6表。
【表6】
第6表
试验例6
在小豆田地(每1个试验区9.6平方米)中,在小豆及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以S-异丙甲草胺为有效成分的EC剂(与前述试验例2相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第39天,用肉眼观察调查自然产生的尼泊尔蓼(NepaleseSmartweed(Persicaria nepalensis(Meisn.)H.Gross))的生长状态,与试验例1同样地进行评价。将结果示于第7表。
【表7】
第7表
试验例7
在扁豆田地(每1个试验区4.8平方米)中,在扁豆及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以氟乐灵为有效成分的EC剂(与前述试验例4相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第49天,用肉眼观察调查自然产生的犬蓼(Oriental lady’s thumb(Persicaria longiseta))的生长状态,与试验例1同样地进行评价。将结果示于第8表。
【表8】
第8表
试验例8
在玉米田地(每1个试验区9.6平方米)中,在玉米及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以S-异丙甲草胺为有效成分的EC剂(与前述试验例2相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第28天,用肉眼观察调查自然产生的藜(common lambsquarters(Chenopodium album L.))的生长状态,与试验例1同样地进行评价。将结果示于第9表。
【表9】
第9表
试验例9
在玉米田地(每1个试验区9.6平方米)中,在玉米及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以S-异丙甲草胺为有效成分的EC剂(与前述试验例2相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第49天,用肉眼观察调查自然产生的反枝苋(redroot pigweed(Amaranthus retroflexus L.))的生长状态,与试验例1同样地进行评价。将结果示于第10表。
【表10】
第10表
试验例10
在玉米田地(每1个试验区9.6平方米)中,在玉米及杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以二甲戊灵为有效成分的EC剂(商品名:ゴーゴーサン乳剂(GOGO SAN NYUZAI),BASF公司制)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第49天,用肉眼观察调查自然产生的蓼科杂草的生长状态,与试验例1同样地进行评价。将结果示于第11表。
【表11】
第11表
试验例11
在播种了马唐(large crabgrass(Digitaria sanguinalis L.))的种子的玉米田地(每1个试验区3.6平方米)中,在马唐达到1.5-2.0叶期时,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以烟嘧磺隆为有效成分的SC剂用含有0.67vol%农业用展着剂(商品名:Actirob B,Bayer CropScience公司制)的水(相当于每1公顷300升)稀释,进行茎叶处理。
在药剂处理后第30天,用肉眼观察调查马唐的生长状态,与试验例1同样地进行评价。将结果示于第12表。
【表12】
第12表
试验例12
在玉米田地(每1个试验区3.6平方米)中,在杂草发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以烟嘧磺隆为有效成分的SC剂用含有0.67vol%的农业用展着剂(与前述试验例11相同)的水(相当于每1公顷300升)稀释,进行土壤处理。
在药剂处理后第30天,用肉眼观察调查自然产生的马齿苋(common purslane(Portulaca oleracea L.))的生长状态,与试验例1同样地进行评价。将结果示于第13表。
【表13】
第13表
试验例13
在1/300,000公顷的箱(pot)中装填土壤,播种苘麻(velvetleaf(Abutilon theophrasti MEDIC.))的种子。在苘麻发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以派罗克杀草砜为有效成分的WG剂(商品名:Sakura 850WG,BayerCropScience公司制)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第12天,用肉眼观察调查苘麻的生长状态,与试验例1同样地进行评价。将结果示于第14表。
【表14】
第14表
试验例14
在1/300,000公顷的箱中装填土壤,播种龙葵(black nightshade(Solanum nigrum L.))的种子。在龙葵发芽前,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以派罗克杀草砜为有效成分的WG剂(与前述试验例13相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第12天,用肉眼观察调查龙葵的生长状态,与试验例1同样地进行评价。将结果示于第15表。
【表15】
第15表
试验例15
在1/300,000公顷的箱中装填土壤,播种稗(barnyardgrass(Echinochloa crus- galli L.))的种子。播种第二天,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以氯苯胺灵为有效成分的EC剂(与前述试验例1相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第21天,用肉眼观察调查稗的生长状态,与试验例1同样地进行评价。将结果示于第16表。
【表16】
第16表
试验例16
将稗(barnyardgrass(Echinochloa crus-galli L.))替换成大狗尾草(giantfoxtail(Setaria faberi Herrm.)),除此之外,与前述试验例15同样地进行试验,得到第17表的结果。其中,有效成分的药量为第17表中所记载的那样。
【表17】
第17表
试验例17
将稗(barnyardgrass(Echinochloa crus-galli L.))替换成龙葵(blacknightshade(Solanum nigrum L.)),除此之外,与前述试验例15同样地进行试验,得到第18表的结果。其中,有效成分的药量为第18表中所记载的那样。
【表18】
第18表
试验例18
在1/300,000公顷的箱中装填土壤,播种稗(barnyardgrass(Echinochloa crus- galli L.))的种子。播种第二天,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以氯苯胺灵为有效成分的EC剂(与前述试验例1相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第26天,用肉眼观察调查稗的生长状态,与试验例1同样地进行评价。将结果示于第19表。
【表19】
第19表
试验例19
将稗(barnyardgrass(Echinochloa crus-galli L.))替换成早熟禾(annualbluegrass(Poa annua L.)),除此之外,与前述试验例18同样地进行试验,得到第20表的结果。其中,有效成分的药量为第20表中所记载的那样。
【表20】
第20表
试验例20
将稗(barnyardgrass(Echinochloa crus-galli L.))替换成藜(commonlambsquarters(Chenopodium album L.)),除此之外,与前述试验例18同样地进行试验,得到第21表的结果。其中,有效成分的药量为第21表中所记载的那样。
【表21】
第21表
试验例21
在1/300,000公顷的箱中装填土壤,播种稗(barnyardgrass(Echinochloa crus- galli L.))的种子。播种第二天,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以扑草净为有效成分的WP剂(商品名:ゲザガード50(Gesagard 50),日本化药株式会社制(Nippon Kayaku Co.,Ltd.))在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第21天,用肉眼观察调查稗的生长状态,与试验例1同样地进行评价。将结果示于第22表。
【表22】
第22表
试验例22
将稗(barnyardgrass(Echinochloa crus-galli L.))替换成马唐(largecrabgrass(Digitaria sanguinalis L.)),除此之外,与前述试验例21同样地进行试验,得到第23表的结果。其中,有效成分的药量为第23表中所记载的那样。
【表23】
第23表
试验例23
在1/300,000公顷的箱中装填土壤,播种龙葵(black nightshade(Solanum nigrum L.))的种子。播种第二天,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以精吡氟禾草灵为有效成分的EC剂(与前述试验例5相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第20天,用肉眼观察调查龙葵的生长状态,与试验例1同样地进行评价。将结果示于第24表。
【表24】
第24表
试验例24
在1/300,000公顷的箱中装填土壤,播种藜(common lambsquarters(Chenopodium album L.))的种子。播种第二天,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以氟乐灵为有效成分的EC剂(与前述试验例4相同)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第21天,用肉眼观察调查藜的生长状态,与试验例1同样地进行评价。将结果示于第25表。
【表25】
第25表
试验例25
将藜(common lambsquarters(Chenopodium album L.))替换成繁缕(commonchickweed(Stellaria media L.)),除此之外,与前述试验例24同样地进行试验,得到第26表的结果。其中,有效成分的药量为第26表中所记载的那样。
【表26】
第26表
试验例26
在1/300,000公顷的箱中装填土壤,播种龙葵(black nightshade(Solanum nigrum L.))的种子。播种第二天,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以苄草丹为有效成分的EC剂(商品名:ボクサー乳剂(BOXER NYUZAI),Syngenta公司制)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第21天,用肉眼观察调查龙葵的生长状态,与试验例1同样地进行评价。将结果示于第27表。
【表27】
第27表
试验例27
将以苄草丹为有效成分的EC剂替换成以氟噻草胺为有效成分的SC剂(商品名:Cadou,Bayer CropScience公司制),除此之外,与前述试验例26同样地进行试验,得到第28表的结果。其中,有效成分的药量为第28表中所记载的那样。
【表28】
第28表
试验例28
在1/300,000公顷的箱中装填土壤,播种马唐(large crabgrass(Digitaria sanguinalis L.))的种子。播种第二天,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以二甲戊灵为有效成分的EC剂(与前述试验例10同样)在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第27天,用肉眼观察调查马唐的生长状态,与试验例1同样地进行评价。将结果示于第29表。
【表29】
第29表
试验例29
在1/300,000公顷的箱中装填土壤,播种马唐(large crabgrass(Digitaria sanguinalis L.))的种子。播种第二天,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以茚草酮为有效成分的WP剂在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第20天,用肉眼观察调查马唐的生长状态,与试验例1同样地进行评价。将结果示于第30表。
【表30】
第30表
试验例30
在1/300,000公顷的箱中装填土壤,播种藜(common lambsquarters(Chenopodium album L.))的种子。播种第二天,将规定量的以溴谷隆为有效成分的SC剂(与前述试验例1相同)及以禾草丹为有效成分的EC剂(商品名:サターン乳剂(Saturn NYUZAI),クミアイ化学工業株式会社制(KUMIAI CHEMICAL INDUSTRY CO.,Ltd.))在相当于每1公顷1000升的水中稀释,进行土壤处理。
在药剂处理后第20天,用肉眼观察调查藜的生长状态,与试验例1同样地进行评价。将结果示于第31表。
【表31】
第31表
试验例31
将藜(common lambsquarters(Chenopodium album L.))替换成龙葵(blacknightshade(Solanum nigrum L.)),除此之外,与前述试验例30同样地进行试验,得到第32表的结果。其中,有效成分的药量为第32表中所记载的那样。
【表32】
第32表
试验例32
与前述试验例18同样地进行试验,得到第33表的结果。其中,有效成分的药量为第33表中所记载的那样。
【表33】
第33表
产业上的可利用性
本发明的除草组合物、及防除或生长抑制方法可应用于水田、旱田、果树园等农耕地、田埂、休耕田、运动场、高尔夫球场、空地、森林、工场地皮、线路旁边、道路旁边等非农耕地等各种领域。
需要说明的是,将于2014年10月22日提出申请的日本专利申请2014-215428号的说明书、权利要求书、及摘要的全部内容引入此处,将其作为本发明的说明书的公开内容并入本文。
Claims (9)
1.一种除草组合物,其含有(A)溴谷隆或其盐、和(B)选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、碘苯腈、二甲戊灵、氟乐灵、苄草丹、禾草丹和茚草酮中的至少1种的除草性化合物、其烷基酯或其盐。
2.根据权利要求1所述的除草组合物,其中,(A)与(B)的混合比率以重量比计为200:1~1:40。
3.一种防除不期望的植物或抑制它们生长的方法,将除草有效量的(A)溴谷隆或其盐、和除草有效量的(B)选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、碘苯腈、二甲戊灵、氟乐灵、苄草丹、禾草丹和茚草酮中的至少1种的除草性化合物、其烷基酯或其盐施用至不期望的植物或它们生长的场所。
4.根据权利要求3所述的方法,其中,施用100~4000g/ha的(A)、20~4000g/ha的(B)。
5.根据权利要求3所述的方法,其中,将(A)和(B)以200:1~1:40的重量比混合施用。
6.根据权利要求1所述的除草组合物,其中,(A)为溴谷隆或其盐,(B)为选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、二甲戊灵、氟乐灵、苄草丹、禾草丹及茚草酮中的至少1种的除草性化合物或其盐。
7.根据权利要求6所述的除草组合物,其中,(A)与(B)的混合比率以重量比计为50:1~1:6。
8.根据权利要求3所述的方法,其中,(A)为溴谷隆或其盐,(B)为选自氯苯胺灵、S-异丙甲草胺、氟噻草胺、派罗克杀草砜、烟嘧磺隆、精吡氟禾草灵、扑草净、二甲戊灵、氟乐灵、苄草丹、禾草丹及茚草酮中的至少1种的除草性化合物或其盐。
9.根据权利要求8所述的方法,其中,将(A)和(B)以50:1~1:6的重量比混合施用。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
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JP2014-215428 | 2014-10-22 | ||
JP2014215428 | 2014-10-22 | ||
PCT/JP2015/079069 WO2016063778A1 (ja) | 2014-10-22 | 2015-10-14 | 除草組成物 |
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CN107072209A true CN107072209A (zh) | 2017-08-18 |
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CN201580057287.4A Pending CN107072209A (zh) | 2014-10-22 | 2015-10-14 | 除草组合物 |
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US (1) | US9993001B2 (zh) |
EP (1) | EP3210473A4 (zh) |
JP (2) | JP6710890B2 (zh) |
KR (1) | KR20170069286A (zh) |
CN (1) | CN107072209A (zh) |
AR (1) | AR102383A1 (zh) |
AU (1) | AU2015334154A1 (zh) |
BR (1) | BR112017008195A2 (zh) |
CA (1) | CA2965466A1 (zh) |
CL (1) | CL2017000972A1 (zh) |
CO (1) | CO2017002773A2 (zh) |
MA (1) | MA40840A (zh) |
MD (1) | MD20170054A2 (zh) |
MX (1) | MX2017005273A (zh) |
PE (1) | PE20170466A1 (zh) |
PH (1) | PH12017500741A1 (zh) |
RU (1) | RU2689555C2 (zh) |
UA (1) | UA119184C2 (zh) |
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EP3342289B1 (en) * | 2016-12-28 | 2020-05-13 | UPL Limited | Herbicidal composition and weed control method |
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CN101562976A (zh) * | 2006-12-21 | 2009-10-21 | 组合化学工业株式会社 | 除草剂组合物 |
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DE3573368D1 (en) | 1984-04-27 | 1989-11-09 | Ciba Geigy Ag | Herbicidal compositions |
MY118564A (en) * | 1998-02-10 | 2004-12-31 | Syngenta Participations Ag | Pesticidal compositions |
US20110028325A1 (en) | 2008-03-18 | 2011-02-03 | Basf Se | Herbicidal Compositions Comprising Pyroxasulfone VI |
BRPI0911207B8 (pt) * | 2008-04-18 | 2022-10-11 | Dow Agrosciences Llc | 2-(fenil substituído)-6-hidróxi ou alcóxi-5-substituído-4-pirimidinacarboxilatos, composição herbicida, e método para controle de vegetação indesejável". |
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JP2013216601A (ja) * | 2012-04-06 | 2013-10-24 | Nippon Nohyaku Co Ltd | 除草剤組成物及びその使用方法 |
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- 2015-10-14 PE PE2017000466A patent/PE20170466A1/es unknown
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- 2015-10-14 MD MDA20170054A patent/MD20170054A2/ro not_active Application Discontinuation
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US5679619A (en) * | 1986-05-23 | 1997-10-21 | American Cyanamid Company | Aqueous suspension concentrate compositions of pendimethalin |
CN101562976A (zh) * | 2006-12-21 | 2009-10-21 | 组合化学工业株式会社 | 除草剂组合物 |
CN103717076A (zh) * | 2011-08-10 | 2014-04-09 | 拜耳知识产权股份有限公司 | 含有特定特特拉姆酸衍生物的活性化合物组合物 |
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WO2016063778A1 (ja) | 2016-04-28 |
AR102383A1 (es) | 2017-02-22 |
CO2017002773A2 (es) | 2017-07-11 |
US9993001B2 (en) | 2018-06-12 |
JP6710890B2 (ja) | 2020-06-17 |
JP2020122026A (ja) | 2020-08-13 |
JPWO2016063778A1 (ja) | 2017-08-03 |
PH12017500741A1 (en) | 2017-10-09 |
MD20170054A2 (ro) | 2017-09-30 |
EP3210473A1 (en) | 2017-08-30 |
PE20170466A1 (es) | 2017-05-06 |
CA2965466A1 (en) | 2016-04-28 |
KR20170069286A (ko) | 2017-06-20 |
MX2017005273A (es) | 2017-08-15 |
RU2017117462A (ru) | 2018-11-23 |
CL2017000972A1 (es) | 2017-11-03 |
UA119184C2 (uk) | 2019-05-10 |
AU2015334154A1 (en) | 2017-06-08 |
RU2689555C2 (ru) | 2019-05-28 |
MA40840A (fr) | 2017-08-29 |
EP3210473A4 (en) | 2018-04-25 |
US20170332642A1 (en) | 2017-11-23 |
BR112017008195A2 (pt) | 2017-12-26 |
RU2017117462A3 (zh) | 2018-12-18 |
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