CN101232813A - 防治杂草的方法 - Google Patents
防治杂草的方法 Download PDFInfo
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- CN101232813A CN101232813A CNA200680028370XA CN200680028370A CN101232813A CN 101232813 A CN101232813 A CN 101232813A CN A200680028370X A CNA200680028370X A CN A200680028370XA CN 200680028370 A CN200680028370 A CN 200680028370A CN 101232813 A CN101232813 A CN 101232813A
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- Prior art keywords
- methyl
- crop
- inhibitor
- phenyl uracils
- grass
- Prior art date
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- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 67
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- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 150000004867 thiadiazoles Chemical class 0.000 description 1
- 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
- 150000007970 thio esters Chemical class 0.000 description 1
- 231100000033 toxigenic Toxicity 0.000 description 1
- 230000001551 toxigenic effect Effects 0.000 description 1
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- 229910001428 transition metal ion Inorganic materials 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
- 125000003866 trichloromethyl group Chemical group ClC(Cl)(Cl)* 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
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 1
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical compound C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
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- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
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- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
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- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
本发明涉及式(I)的3-苯基尿嘧啶任选与一种或多种其他除草剂B组合以及任选与一种或多种安全剂C组合在防治抗草甘膦杂草或作物中的用途,其中变量R1-R7如说明书所定义。
Description
本发明涉及一种防治抗草甘膦(glyphosate)杂草或作物的方法。
抗草甘膦杂草对于有效的杂草防治产生严重问题,因为该类抗性杂草日益广泛且因为通过施用草甘膦防治杂草不再有效。此外,在某些情况下,抗草甘膦作物,如Roundup Ready油菜、玉米或棉花可能在它们偶然萌发(“自生作物”)以及在本身抗草甘膦并且其中杂草防治通过使用草甘膦实现的随后倒茬作物中生长时产生严重问题。因此需要一种防治抗草甘膦杂草或作物的有效方法。
已知苯基尿嘧啶为有用的除草剂。将除草的苯基尿嘧啶用作干燥剂和/或脱叶剂公开于WO 01/83459中。此外,由WO 03/24221已知包含苯基尿嘧啶I或其可农用盐和包括草甘膦在内的其他除草剂和/或某些安全剂的组合呈现协同增强的活性:
其中变量R1-R7如下所定义:
R1为甲基或NH2;
R2为C1-C2卤代烷基;
R3为氢或卤素;
R4为卤素或氰基;
R5为氢、氰基、C1-C6烷基、C1-C6烷氧基、C1-C4烷氧基-C1-C4烷基、C3-C7环烷基、C3-C6链烯基、C3-C6炔基或未被取代或被卤素或烷基取代的苄基;
R6、R7相互独立地为氢、C1-C6烷基、C1-C6烷氧基、C3-C6链烯基、C3-C6炔基、C3-C7环烷基、C3-C7环烯基、苯基或苄基,其中上述8个取代基各自未被取代或可以被1-6个卤原子取代和/或可以被1、2或3个选自如下的基团取代:OH、NH2、CN、CONH2、C1-C4烷氧基、C1-C4卤代烷氧基、C1-C4烷硫基、C1-C4卤代烷硫基、C1-C4烷基磺酰基、C1-C4卤代烷基磺酰基、C1-C4烷基氨基、二(C1-C4烷基)氨基、甲酰基、C1-C4烷基羰基、C1-C4烷氧羰基、C1-C4烷基氨基羰基、二(C1-C4烷基)氨基羰基、C3-C7环烷基、苯基和苄基;或
R6、R7与氮原子一起形成可以被1-6个甲基取代且可以另外含有1或2个选自氮、氧和硫的杂原子作为环成员的3、4、5、6或7员饱和或不饱和氮杂环。
WO 04/080183公开了所述苯基尿嘧啶与某些其他除草剂的组合,它们具有增强的除草活性和与有用植物的改善相容性。
惊人的是,现已发现苯基尿嘧啶或其可农用盐任选与至少一种其他除草剂组合和/或任选与至少一种安全剂组合对于防治抗草甘膦杂草或作物特别有效。
本发明此外还涉及一种防治抗草甘膦杂草或作物的方法,包括使除草有效量的式I的3-苯基尿嘧啶或其可农用盐(组分A):
其中变量R1-R7如下所定义:
R1为甲基或NH2;
R2为C1-C2卤代烷基;
R3为氢或卤素;
R4为卤素或氰基;
R5为氢或C1C6烷基;
R6、R7相互独立地为氢、C1-C6烷基、C1-C6烷氧基、C3-C6链烯基、C3-C6炔基、C3-C7环烷基、C3-C7环烯基、苯基或苄基;作用于抗草甘膦杂草或作物或其生长场所。
生长场所是指植物的生存空间。
在式I中的取代基R2、R5、R6、R7的定义中提到的有机结构部分象术语卤素一样是各所列基团成员的集合性术语。所有烃链,即所有烷基、卤代烷基、环烷基、烷氧基、环烯基、链烯基和炔基可以是直链或支化的,其中前缀Cn-Cm在每种情况下表示该基团中的可能碳原子数。卤代取代基优选带有1、2、3、4或5个相同或不同的卤原子。术语卤素在每种情况下表示氟、氯、溴或碘。
该类含义的实例是:
-C1-C4烷基:CH3、C2H5、正丙基、CH(CH3)2、正丁基、CH(CH3)-C2H5、CH2-CH(CH3)2和C(CH3)3;
-C1-C6烷基:上述C1-C4烷基以及例如正戊基、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、正己基、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-甲基丙基或1-乙基-2-甲基丙基,优选甲基、乙基、正丙基、1-甲基乙基、正丁基、1,1-二甲基乙基、正戊基或正己基;
-C1-C2卤代烷基:部分或完全被氟、氯、溴和/或碘取代的甲基或乙基,例如CH2F、CHF2、CF3、CH2Cl、二氯甲基、三氯甲基、氯氟甲基、二氯一氟甲基、一氯二氟甲基、2-氟乙基、2-氯乙基、2-溴乙基、2-碘乙基、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、C2F5;
-C1-C4烷氧基:OCH3、OC2H5、正丙氧基、OCH(CH3)2、正丁氧基、OCH(CH3)-C2H5、OCH2-CH(CH3)2或OC(CH3)3,优选OCH3、OC2H5或OCH(CH3)2;
-C1-C6烷氧基:上述C1-C4烷氧基以及例如戊氧基、1-甲基丁氧基、2-甲基丁氧基、3-甲氧基丁氧基、1,1-二甲基丙氧基、1,2-二甲基丙氧基、2,2-二甲基丙氧基、1-乙基丙氧基、己氧基、1-甲基戊氧基、2-甲基戊氧基、3-甲基戊氧基、4-甲基戊氧基、1,1-二甲基丁氧基、1,2-二甲基丁氧基、1,3-二甲基丁氧基、2,2-二甲基丁氧基、2,3-二甲基丁氧基、3,3-二甲基丁氧基、1-乙基丁氧基、2-乙基丁氧基、1,1,2-三甲基丙氧基、1,2,2-三甲基丙氧基、1-乙基-1-甲基丙氧基和1-乙基-2-甲基丙氧基;
-C3-C6链烯基:丙-1-烯-1-基、烯丙基、1-甲基乙烯基、1-丁烯-1-基、1-丁烯-2-基、1-丁烯-3-基、2-丁烯-1-基、1-甲基丙-1-烯-1-基、2-甲基丙-1-烯-1-基、1-甲基丙-2-烯-1-基、2-甲基丙-2-烯-1-基、正戊烯-1-基、正戊烯-2-基、正戊烯-3-基、正戊烯-4-基、1-甲基丁-1-烯-1-基、2-甲基丁-1-烯-1-基、3-甲基丁-1-烯-1-基、1-甲基丁-2-烯-1-基、2-甲基丁-2-烯-1-基、3-甲基丁-2-烯-1-基、1-甲基丁-3-烯-1-基、2-甲基丁-3-烯-1-基、3-甲基丁-3-烯-1-基、1,1-二甲基丙-2-烯-1-基、1,2-二甲基丙-1-烯-1-基、1,2-二甲基丙-2-烯-1-基、1-乙基丙-1-烯-2-基、1-乙基丙-2-烯-1-基、正己-1-烯-1-基、正己-2-烯-1-基、正己-3-烯-1-基、正己-4-烯-1-基、正己-5-烯-1-基、1-甲基戊-1-烯-1-基、2-甲基戊-1-烯-1-基、3-甲基戊-1-烯-1-基、4-甲基戊-1-烯-1-基、1-甲基戊-2-烯-1-基、2-甲基戊-2-烯-1-基、3-甲基戊-2-烯-1-基、4-甲基戊-2-烯-1-基、1-甲基戊-3-烯-1-基、2-甲基戊-3-烯-1-基、3-甲基戊-3-烯-1-基、4-甲基戊-3-烯-1-基、1-甲基戊-4-烯-1-基、2-甲基戊-4-烯-1-基、3-甲基戊-4-烯-1-基、4-甲基戊-4-烯-1-基、1,1-二甲基丁-2-烯-1-基、1,1-二甲基丁-3-烯-1-基、1,2-二甲基丁-1-烯-1-基、1,2-二甲基丁-2-烯-1-基、1,2-二甲基丁-3-烯-1-基、1,3-二甲基丁-1-烯-1-基、1,3-二甲基丁-2-烯-1-基、1,3-二甲基丁-3-烯-1-基、2,2-二甲基丁-3-烯-1-基、2,3-二甲基丁-1-烯-1-基、2,3-二甲基丁-2-烯-1-基、2,3-二甲基丁-3-烯-1-基、3,3-二甲基丁-1-烯-1-基、3,3-二甲基丁-2-烯-1-基、1-乙基丁-1-烯-1-基、1-乙基丁-2-烯-1-基、1-乙基丁-3-烯-1-基、2-乙基丁-1-烯-1-基、2-乙基丁-2-烯-1-基、2-乙基丁-3-烯-1-基、1,1,2-三甲基丙-2-烯-1-基、1-乙基-1-甲基丙-2-烯-1-基、1-乙基-2-甲基丙-1-烯-1-基或1-乙基-2-甲基丙-2-烯-1-基;
-C3-C6炔基:丙-1-炔-1-基、丙-2-炔-1-基、正丁-1-炔-1-基、正丁-1-炔-3-基、正丁-1-炔-4-基、正丁-2-炔-1-基、正戊-1-炔-1-基、正戊-1-炔-3-基、正戊-1-炔-4-基、正戊-1-炔-5-基、正戊-2-炔-1-基、正戊-2-炔-4-基、正戊-2-炔-5-基、3-甲基丁-1-炔-3-基、3-甲基丁-1-炔-4-基、正己-1-炔-1-基、正己-1-炔-3-基、正己-1-炔-4-基、正己-1-炔-5-基、正己-1-炔-6-基、正己-2-炔-1-基、正己-2-炔-4-基、正己-2-炔-5-基、正己-2-炔-6-基、正己-3-炔-1-基、正己-3-炔-2-基、3-甲基戊-1-炔-1-基、3-甲基戊-1-炔-3-基、3-甲基戊-1-炔-4-基、3-甲基戊-1-炔-5-基、4-甲基戊-1-炔-1-基、4-甲基戊-2-炔-4-基或4-甲基戊-2-炔-5-基,优选丙-2-炔-1-基;
-C3-C7环烷基:具有3-7个环成员的单环饱和烃环,如环丙基、环丁基、环戊基、环己基或环庚基;
-C3-C7环烯基:具有3-7个环成员的单环不饱和烃环,如环丙-1-烯基、环丙-2-烯基、环丁-1-烯基、环丁-2-烯基、环丁-1,3-二烯基、环戊-1-烯基、环戊-2-烯基、环戊-3-烯基、环戊-2,4-二烯基、环己-1-烯基、环己-2-烯基、环己-3-烯基、环己-1,3-二烯基、环己-1,5-二烯基、环己-2,4-二烯基或环己-2,5-二烯基。
可以使用一种或多种3-苯基尿嘧啶。
当抗草甘膦作物在不同于前一作物的随后倒茬作物中偶然和非刻意生长时要求防治抗草甘膦作物。
在式I的3-苯基尿嘧啶中,优选其中变量R1-R7相互独立地具有下列含义的那些:
R1为甲基或NH2;
R2为三氟甲基;
R3为氢、氟或氯,尤其是氟;
R4为卤素或氰基,尤其是氯或氰基;
R5为氢;
R6、R7相互独立地为氢或C1-C6烷基。
R6和R7尤其为相同或不同的C1-C6烷基。
本发明的特别优选实施方案包括其中在式I中各变量R1-R7具有下列含义的至少一种3-苯基尿嘧啶I(下文也称为苯基尿嘧啶Ia)的用途:
R1为甲基;
R2为三氟甲基;
R3为氟;
R4为氯;
R5为氢;
R6、R7相互独立地为C1-C6烷基。
本发明的另一特别优选实施方案包括在式I中各变量R1-R7具有下列含义的至少一种3-苯基尿嘧啶I(下文也称为苯基尿嘧啶Ib)的用途:
R1为NH2;
R2为三氟甲基;
R3为氟;
R4为氯;
R5为氢;
R6、R7相互独立地为C1-C6烷基。
特别优选的除草剂Ia或Ib的实例是下列式I’的3-苯基尿嘧啶,其中R1、R6和R7具有表1的一行所给含义(化合物I.1-I.74)。
表1
3-苯基尿嘧啶I | R1 | R6 | R7 |
I.1 | 甲基 | 甲基 | 甲基 |
I.2 | 氨基 | 甲基 | 甲基 |
I.3 | 甲基 | 甲基 | 乙基 |
I.4 | 氨基 | 甲基 | 乙基 |
I.5 | 甲基 | 甲基 | 丙基 |
I.6 | 氨基 | 甲基 | 丙基 |
I.7 | 甲基 | 甲基 | 异丙基 |
3-苯基尿嘧啶I | R1 | R6 | R7 |
I.8 | 氨基 | 甲基 | 异丙基 |
I.9 | 甲基 | 甲基 | 丁基 |
I.10 | 氨基 | 甲基 | 丁基 |
I.11 | 甲基 | 甲基 | 仲丁基 |
I.12 | 氨基 | 甲基 | 仲丁基 |
I.13 | 甲基 | 甲基 | 异丁基 |
I.14 | 氨基 | 甲基 | 异丁基 |
I.15 | 甲基 | 甲基 | 叔丁基 |
I.16 | 氨基 | 甲基 | 叔丁基 |
I.17 | 甲基 | 甲基 | 正戊基 |
I.18 | 氨基 | 甲基 | 正戊基 |
I.19 | 甲基 | 甲基 | 正己基 |
I.20 | 氨基 | 甲基 | 正己基 |
I.21 | 甲基 | 甲基 | 烯丙基 |
I.22 | 氨基 | 甲基 | 烯丙基 |
I.23 | 甲基 | 甲基 | 炔丙基 |
I.24 | 氨基 | 甲基 | 炔丙基 |
I.25 | 甲基 | 甲基 | 苯基 |
I.26 | 氨基 | 甲基 | 苯基 |
I.27 | 甲基 | 甲基 | 苄基 |
I.28 | 氨基 | 甲基 | 苄基 |
I.29 | 甲基 | 乙基 | 乙基 |
I.30 | 氨基 | 乙基 | 乙基 |
I.31 | 甲基 | 乙基 | 丙基 |
I.32 | 氨基 | 乙基 | 丙基 |
I.33 | 甲基 | 乙基 | 异丙基 |
I.34 | 氨基 | 乙基 | 异丙基 |
I.35 | 甲基 | 乙基 | 丁基 |
I.36 | 氨基 | 乙基 | 丁基 |
I.37 | 甲基 | 乙基 | 正戊基 |
I.38 | 氨基 | 乙基 | 正戊基 |
I.39 | 甲基 | 乙基 | 正己基 |
I.40 | 氨基 | 乙基 | 正己基 |
I.41 | 甲基 | 丙基 | 丙基 |
3-苯基尿嘧啶I | R1 | R6 | R7 |
I.42 | 氨基 | 丙基 | 丙基 |
I.43 | 甲基 | 丙基 | 异丙基 |
I.44 | 氨基 | 丙基 | 异丙基 |
I.45 | 甲基 | 丙基 | 丁基 |
I.46 | 氨基 | 丙基 | 丁基 |
I.47 | 甲基 | 丙基 | 正戊基 |
I.48 | 氨基 | 丙基 | 正戊基 |
I.49 | 甲基 | 丙基 | 正己基 |
I.50 | 氨基 | 丙基 | 正己基 |
I.51 | 甲基 | 异丙基 | 异丙基 |
I.52 | 氨基 | 异丙基 | 异丙基 |
I.53 | 甲基 | 异丙基 | 丁基 |
I.54 | 氨基 | 异丙基 | 丁基 |
I.55 | 甲基 | 异丙基 | 正戊基 |
I.56 | 氨基 | 异丙基 | 正戊基 |
I.57 | 甲基 | 异丙基 | 正己基 |
I.58 | 氨基 | 异丙基 | 正己基 |
I.59 | 甲基 | 丁基 | 丁基 |
I.60 | 氨基 | 丁基 | 丁基 |
I.61 | 甲基 | 丁基 | 正戊基 |
I.62 | 氨基 | 丁基 | 正戊基 |
I.63 | 甲基 | 丁基 | 正己基 |
I.64 | 氨基 | 丁基 | 正己基 |
I.65 | 甲基 | 正戊基 | 正戊基 |
I.66 | 氨基 | 正戊基 | 正戊基 |
I.67 | 甲基 | 正戊基 | 正己基 |
I.68 | 氨基 | 正戊基 | 正己基 |
I.69 | 甲基 | 正己基 | 正己基 |
I.70 | 氨基 | 正己基 | 正己基 |
I.71 | 甲基 | -(CH2)4- | |
I.72 | 氨基 | -(CH2)4- | |
I.73 | 甲基 | -(CH2)2-O-(CH2)2- | |
I.74 | 氨基 | -(CH2)2-O-(CH2)2- |
特别优选化合物I.1、I.3、I.5、I.7、I.9、I.11和I.13。
优选式I的3-苯基尿嘧啶与至少一种(一种或多种)其他除草剂(组分B)或其可农用盐或衍生物(条件是该除草剂具有羧基)组合使用。除草剂B选自下列b1)-b15)类:
b1)类脂生物合成抑制剂;
b2)乙酰乳酸酯合成酶抑制剂(ALS抑制剂);
b3)光合成抑制剂;
b4)原卟啉原-IX氧化酶抑制剂;
b5)白化除草剂;
b6)烯醇丙酮酰基莽草酸3-磷酸酯合成酶抑制剂(EPSP抑制剂);
b7)谷氨酰胺合成酶抑制剂;
b8)7,8-二氢蝶酸酯合成酶抑制剂(DHP抑制剂);
b9)有丝分裂抑制剂;
b10)长链脂肪酸合成抑制剂(VLCFA抑制剂);
b11)纤维素生物合成抑制剂;
b12)去偶除草剂;
b13)植物生长素除草剂;
b14)植物生长素输送抑制剂;
b15)选自新燕灵(benzoylprop)、氟燕灵(flamprop)、强氟燕灵(flamprop-M)、溴丁酰草胺(bromobutide)、氯甲丹(chlorflurenol)、环庚草醚(cinmethylin)、苯丙隆(methyldymuron)、乙苯酰草(etobenzanid)、膦铵素(fosamine)、威百亩(metam)、稗草畏(pyributicarb)、氯嗪草(oxaziclomefone)、棉隆(dazomet)、苯氧丙胺津(triaziflam)和溴甲烷的其他除草剂。
优选的b1)-b15)类除草剂为下列化合物:
b1)类脂生物合成抑制剂:炔禾灵(chlorazifop)、炔草酯(clodinafop)、氯丁草(clofop)、氰氟草酯(cyhalofop)、氯甲草(diclofop)、唑禾草灵(fenoxaprop)、高唑禾草灵(fenoxaprop-p)、噻唑禾草灵(fenthiaprop)、吡氟禾草灵(fluazifop)、精吡氟禾草灵(fluazifop-P)、吡氟氯禾灵(haloxyfop)、精吡氟氯禾灵(haloxyfop-P)、恶草醚(isoxapyrifop)、唑酰草胺(metamifop)、喔草酯(propaquizafop)、喹禾灵(quizalofop)、精喹禾灵(quizalofop-P)、三氟苯氧丙酸(trifop)、枯杀达(alloxydim)、丁氧环酮(butroxydim)、烯草酮(clethodim)、环己烯草酮(cloproxydim)、噻草酮(cycloxydim)、环苯草酮(profoxydim)、稀禾定(sethoxydim)、醌肟草(tepraloxydim)、肟草酮(tralkoxydim)、苏达灭(butylate)、草灭特(cycloate)、燕麦敌(diallate)、哌草丹(dimepiperate)、扑草灭(EPTC)、禾草畏(esprocarb)、抑草威(ethiolate)、氮草(isopolinate)、甲硫苯威(methiobencarb)、草达灭(molinate)、坪草丹(orbencarb)、克草猛(pebulate)、苄草丹(prosulfocarb)、草克死(sulfallate)、杀草丹(thiobencarb)、丁草威(tiocarbazil)、野麦畏(triallate)、灭草猛(vernolate)、呋草黄(benfuresate)、乙呋草黄(ethofumesate)、地散磷(bensulide)和pinoxaden;
b2)ALS抑制剂:磺氨黄隆(amidosulfuron)、四唑黄隆(azimsulfuron)、苄嘧黄隆(bensulfuron)、氯嘧黄隆(chlorimuron)、绿黄隆(chlorsulfuron)、醚黄隆(cinosulfuron)、环丙黄隆(cyclosulfamuron)、胺苯黄隆(ethametsulfuron)、乙氧嘧黄隆(ethoxysulfuron)、啶嘧黄隆(flazasulfuron)、氟啶黄隆(flupyrsulfuron)、甲酰胺黄隆(foramsulfuron)、吡氯黄隆(halosulfuron)、啶咪黄隆(imazosulfuron)、碘黄隆(iodosulfuron)、甲基二黄隆(mesosulfuron)、甲黄隆(metsulfuron)、烟黄隆(nicosulfuron)、环丙氧黄隆(oxasulfuron)、氟嘧黄隆(primisulfuron)、氟丙黄隆(prosulfuron)、吡嘧黄隆(pyrazosulfuron)、玉嘧黄隆(rimsulfuron)、嘧黄隆(sulfometuron)、乙黄黄隆(sulfosulfuron)、噻黄隆(thifensulfuron)、醚苯黄隆(triasulfuron)、苯黄隆(tribenuron)、三氟啶黄隆(trifloxysulfuron)、氟胺磺隆(triflusulfuron)、三氟甲磺隆(tritosulfuron)、咪草酯(imazamethabenz)、咪草啶酸(imazamox)、甲基咪草烟(imazapic)、灭草烟(imazapyr)、灭草喹(imazaquin)、咪草烟(imazethapyr)、唑嘧磺胺盐(cloransulam)、唑嘧磺胺(diclosulam)、双氟磺草胺(florasulam)、氟唑啶草(flumetsulam)、唑草磺胺(metosulam)、五氟磺草胺(penoxsulam)、双嘧苯甲酸(bispyribac)、肟啶草(pyriminobac)、丙苯磺隆(propoxycarbazone)、氟酮黄隆(flucarbazone)、嘧苯草肟(pyribenzoxim)、环酯草醚(pyriftalid)、嘧硫苯甲酸(pyrithiobac)、flucetosulfuron、orthosulfamuron、pyrimisulfan、由WO 02/36595已知的[N-(5,7-二甲氧基[1,2,4]三唑并[1,5-a]嘧啶-2-基-2-甲氧基-4-(三氟甲基)-3-吡啶磺酰胺;
b3)光合成抑制剂:阿特拉通(atraton)、莠去津(atrazine)、莠灭净(ametryne)、叠氮津(aziprotryne)、草净津(cyanazine)、硫草净津(cyanatryn)、可乐津(chlorazine)、环草津(cyprazine)、敌草净(desmetryne)、戊草津(dimethametryne)、杀草净(dipropetryn)、草止津(eglinazine)、草怕津(ipazine)、麦苏百津(mesoprazine)、醚草通(methometon)、盖草津(methoprotryne)、环氰津(procyazine)、丙草止津(proglinazine)、扑灭通(prometon)、扑草净(prometryne)、扑灭津(propazine)、另丁津(sebuthylazine)、密草通(secbumeton)、西玛津(simazine)、西玛通(simeton)、西草净(simetryne)、甲氧去草净terbumeton)、特丁津(terbuthylazine)、去草净(terbutryne)、草达津(trietazine)、特津酮(ametridione)、特草嗪酮(amibuzin)、六嗪同(hexazinone)、嗪丁草(isomethiozin)、苯嗪草(metamitron)、赛克津(metribuzin)、除草定(bromacil)、异草定(isocil)、环草定(lenacil)、特草定(terbacil)、溴杀草敏(brompyrazon)、杀草敏(chloridazon)、敌米达松(dimidazon)、异苯敌草(desmedipham)、敌克草(phenisopham)、苯敌草(phenmedipham)、乙苯敌草(phenmedipham-ethyl)、噻草隆(benzthiazuron)、丁噻隆(buthiuron)、噻二唑隆(ethidimuron)、异恶隆(isouron)、噻唑隆(methabenzthiazuron)、monoisouron、丁唑隆(tebuthiuron)、赛唑隆(thiazafluron)、疏草隆(anisuron)、播土隆(buturon)、氯溴隆(chlorbromuron)、乙氧苯隆(chloreturon)、绿麦隆(chlorotoluron)、枯草隆(chloroxuron)、枯莠隆(difenoxuron)、丁隆(dimefuron)、敌草隆(diuron)、非草隆(fenuron)、伏草隆(fluometuron)、氟苯隆(fluothiuron)、异丙隆(isoproturon)、利谷隆(linuron)、灭草恒(methiuron)、色满隆(metobenzuron)、秀谷隆(metobromuron)、甲氧隆(metoxuron)、绿谷隆(monolinuron)、灭草隆(monuron)、草不隆(neburon)、对伏隆(parafluron)、稀草隆(phenobenzuron)、环草隆(siduron)、氟氧隆(tetrafluron)、赛二唑素(thidiazuron)、莎草快(cyperquat)、二乙除草双(diethamquat)、苯敌快(difenzoquat)、敌草快阳离子(diquat)、伐草快(morfamquat)、对草快(paraquat)、糠草腈(bromobonil)、溴苯腈(bromoxynil)、羟敌草腈(chloroxynil)、碘草腈(iodobonil)、碘苯腈(ioxynil)、氨唑草酮(amicarbazone)、杀草全(bromofenoxim)、三氟嗪(flumezin)、灭草定(methazole)、噻草平(bentazone)、敌稗(propanil)、蔬草灭(pentanochlor)、达草止(pyridate)和pyridafol;
b4)原卟啉原-IX氧化酶抑制剂:氟锁草醚(acifluorfen)、治草醚(bifenox)、氯硝醚(chlomethoxyfen)、草枯醚(chlornitrofen)、氯氟草醚(ethoxyfen)、消草醚(fluorodifen)、乙羧氟草醚(fluoroglycofen)、氯草醚(fluoronitrofen)、氟黄胺草醚(fomesafen)、氟呋草醚(furyloxyfen)、氟硝磺酰胺(halosafen)、乳氟禾草灵(lactofen)、除草醚(nitrofen)、硝氟草醚(nitrofluorfen)、乙氧氟草醚(oxyfluorfen)、异丙吡草酯(fluazolate)、氟唑草(pyraflufen)、吲哚酮草酯(cinidon-ethyl)、酰亚胺苯氧乙酸(flumiclorac)、氟嗪酮(flumioxazin)、炔草胺(flu mipropyn)、达草氟(fluthiacet)、噻二唑胺(thidiazimin)、恶草灵(oxadiazon)、炔丙唑草(oxadiargyl)、唑啶炔草(azafenidin)、氟酮唑草(carfentrazone)、磺胺草唑(sulfentrazone)、戊唑草(pentoxazone)、双苯嘧草酮(benzfendizone)、氟丙嘧草酯(butafenacil)、双唑草腈(pyraclonil)、氟唑草胺(profluazol)、flufenpyr、flupropacil、吡氯草胺(nipyraclofen)、乙胺草醚(etnipromid)和bencarbazone;
b5)白化除草剂:氟哒草(metflurazon)、达草灭(norflurazon)、氟苯啶草(flufenican)、吡氟草胺(diflufenican)、氟吡酰草胺(picolinafen)、氟丁酰草胺(beflubutamid)、氟草同(fluridone)、氟咯草酮(flurochloridone)、呋草酮(flurtamone)、硝磺酮(mesotrione)、磺草酮(sulcotrione)、氯草酮(isoxachlortole)、异氟草(isoxaflutole)、吡草酮(benzofenap)、吡唑特(pyrazolynate)、苄草唑(pyrazoxyfen)、苯并双环酮(benzobicyclon)、杀草强(amitrole)、异恶草酮(clomazone)、苯草醚(aclonifen)、由EP 723960已知的4-(3-三氟甲基苯氧基)-2-(4-三氟甲基苯基)嘧啶、topramezone、由WO 00/15615已知的4-羟基-3-{[2-甲基-6-(三氟甲基)-3-吡啶基]羰基}双环[3.2.1]辛-3-烯-2-酮、由WO01/94339已知的4-羟基-3-{[2-(2-甲氧基乙氧基)甲基-6-(三氟甲基)-3-吡啶基]羰基}双环[3.2.1]辛-3-烯-2-酮、由EP 338992已知的4-羟基-3-[4-(甲基磺酰基)-2-硝基苯甲酰基]双环[3.2.1]-辛-3-烯-2-酮、2-[2-氯-4-(甲基磺酰基)-3-[(2,2,2-三氟乙氧基)甲基]苯甲酰基]-3-羟基-2-环己烯-1-酮(由DE 19846792已知)和pyrasulfotole;
b6)EPSP合成酶抑制剂:草甘膦;
b7)谷氨酰胺合成酶抑制剂:草铵膦(glufosinate)和双丙氨酰膦(bilanaphos);
b8)DHP合成酶抑制剂:黄草灵(asulam);
b9)有丝分裂抑制剂:氟草胺(benfluralin)、地乐胺(butralin)、敌乐胺(dinitramine)、丁氟消草(ethalfluralin)、氟消草(fluchloralin)、异乐灵(isopropalin)、氟烯硝草(methalpropalin)、磺乐灵(nitralin)、黄草消(oryzalin)、胺硝草(pendimethalin)、氨基丙氟灵(prodiamine)、卡乐施(profluralin)、氟乐灵(trifluralin)、甲基胺草磷(amiprofos-methyl)、草胺磷(butamifos)、氟硫草定(dithiopyr)、噻氟啶草(thiazopyr)、拿草特(propyzamide)、丙戊草胺(tebutam)、敌草索(chlorthal)、长杀草(carbetamide)、氯草灵(chlorbufam)、氯苯胺灵(chlorpropham)和苯胺灵(propham);
b10)VLCFA抑制剂:乙草胺(acetochlor)、甲草胺(alachlor)、丁草胺(butachlor)、丁烯草胺(butenachlor)、敌草乐(delachlor)、安塔(diethatyl)、克草胺(dimethachlor)、噻吩草胺(dimethenamid)、精噻吩草胺(dimethenamid-P)、吡草胺(metazachlor)、异丙甲草胺(metolachlor)、S-异丙甲草胺(S-metolachlor)、丙草胺(pretilachlor)、毒草安(propachlor)、异丙草胺(propisochlor)、广草胺(prynachlor)、猛杀草(terbuchlor)、噻醚草胺(thenylchlor)、二甲苯草胺(xylachlor)、草毒死(allidochlor)、草立死(CDEA)、磺唑草(epronaz)、草乃敌(diphenamid)、草萘胺(napropamide)、草萘胺(naproanilide)、烯草胺(pethoxamid)、氟噻草胺(flufenacet)、苯噻草胺(mefenacet)、四唑草胺(fentrazamide)、莎稗磷(anilofos)、哌草磷(piperophos)、唑草胺(cafenstrole)、茚草酮(indanofan)和灭草环(tridiphane);
b11)纤维素生物合成抑制剂:敌草腈(dichlobenil)、草克乐(chlorthiamid)、异恶草胺(isoxaben)和唑草胺(flupoxam);
b12)去偶除草剂:消草酯(dinofenate)、硝丙酚(dinoprop)、戊硝酚(dinosam)、地乐酚(dinoseb)、地乐消酚(dinoterb)、二硝甲酚(DNOC)、硝草酚(etinofen)和丁硝酚(medinoterb);
b13)植物生长素除草剂:稗草胺(clomeprop)、2,4-滴(2,4-D)、2,4,5-涕(2,4,5-T)、2甲4氯(MCPA)、酚硫杀(MCPA thioethyl)、2,4-滴丙酸(dichlorprop)、高2,4-滴丙酸(dichlorprop-P)、2甲4氯丙酸(mecoprop)、高2甲4氯丙酸(mecoprop-P)、2,4-滴丁酸(2,4-DB)、2甲4氯丁酸(MCPB)、草灭平(chloramben)、麦草畏(dicamba)、草芽平(2,3,6-TBA)、杀草畏(tricamba)、二氯喹啉酸(quinclorac)、喹草酸(quinmerac)、二氯皮考啉酸(clopyralid)、氟草烟(fluroxypyr)、毒莠定(picloram)、定草酯(triclopyr)、草除灵(benazolin)和aminopyralid;
b14)植物生长素输送抑制剂:抑草生(naptalam)、二氟吡隆(diflufenzopyr);
b15)新燕灵(benzoylprop)、氟燕灵(flamprop)、强氟燕灵(flamprop-M)、溴丁酰草胺(bromobutide)、氯甲丹(chlorflurenol)、环庚草醚(cinmethylin)、苯丙隆(methyldymuron)、乙苯酰草(etobenzanid)、膦铵素(fosamine)、威百亩(metam)、稗草畏(pyributicarb)、氯嗪草、棉隆、苯氧丙胺津、溴甲烷;
这些除草剂的可农用盐和可农用衍生物,条件是它们具有羧基。
根据优选实施方案,将3-苯基尿嘧啶I与草甘膦或其可农用盐组合使用。
根据另一优选实施防护按,将3-苯基尿嘧啶I与草甘膦和至少一种(一种或多种)其他除草剂B,优选选自所述b1)-b5)和b7)-b15)类的除草剂B或其可农用盐或衍生物组合使用。
此外,式I的3-苯基尿嘧啶任选与所述至少一种除草剂B组合可以与至少一种(一种或多种)安全剂(组分C)或其可农用盐或可农用衍生物组合使用,条件是所述安全剂具有羧基。安全剂优选选自解草酮(benoxacor)、喹氧乙酸(cloquintocet)、抑害腈(cyometrinil)、抑害胺(dichlormid)、dicyclonon、dietholate、解草唑(fenchlorazole)、解草啶(fenclorim)、解草安(flurazole)、肟草安(fluxofenim)、解草呋(furilazole)、双苯唑酸(isoxadifen)、吡咯二酸(mefenpyr)、mephenate、萘二甲酐、2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷(R-29148)、4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷(AD-67、MON 4660)和解草腈(oxabetrinil),包括它们的可农用盐以及当它们具有羧基时,还包括它们的可农用衍生物。
根据另一优选实施方案,将3-苯基尿嘧啶I与草甘膦或其可农用盐、至少一种其他除草剂B,优选选自所述b1)-b5)和b6)-b15)类的除草剂B,或其可农用盐或可农用衍生物和至少一种(一种或多种)安全剂C或其可农用盐或衍生物组合使用。
b1)-b15)类除草剂B和活性化合物C是已知的除草剂和安全剂,参见所引用的参考文献以及例如The Compendium of Pesticide CommonNames(http://www.hclrss.demon.co.uk/index.html);Farm ChemicalsHandbook 2000,第86卷,Meister Publishing Company,2000;B.Hock,C.Fedtke,R.R.Schmidt,Herbizide,Georg Thieme Verlag,Stuttgart1995;W.H.Ahrens,Herbicide Handbook,第7版,Weed Science Societyof America,1994;和K.K.Hatzios,Herbicide Handbook,第7版的增补,Weed Science Society of America,1998。2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷[CAS No.52836-31-4]也以名称R-29148已知。4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷[CAS No.71526-07-03]也以名称AD-67和MON 4660已知。
活性化合物根据其作用模式的分类基于现行理解。若活性化合物通过不止一种作用模式起作用,则该物质仅归属于一种作用模式。
若苯基尿嘧啶I、除草剂B和/或安全剂C能够形成几何异构体,例如E/Z异构体,则可以在本发明组合物中使用纯异构体及其混合物。若苯基尿嘧啶I、除草剂B和/或安全剂C具有一个或多个手性中心且因此以对映体或非对映体存在,则可以在本发明组合物中使用纯对映体和非对映体及其混合物。
若苯基尿嘧啶I、除草剂B和/或安全剂C具有可以被离子化的官能基团,则它们还可以其可农用盐形式使用。通常而言,合适的是对活性化合物的作用没有不利影响的那些阳离子的盐或其阳离子和阴离子分别对活性化合物的作用没有不利影响的那些酸的酸加成盐。
优选的阳离子是碱金属离子,优选锂、钠和钾离子,碱土金属离子,优选钙和镁离子,以及过渡金属离子,优选锰、铜、锌和铁离子,此外还有铵和其中1-4个氢原子被C1-C4烷基、羟基-C1-C4烷基、C1-C4烷氧基-C1-C4烷基、羟基-C1-C4烷氧基-C1-C4烷基、苯基或苄基替代的取代铵,优选铵、甲基铵、异丙基铵、二甲基铵、二异丙基铵、三甲基铵、四甲基铵、四乙基铵、四丁基铵、2-羟基乙基铵、2-(2-羟基乙氧基)乙-1-基铵、二(2-羟基乙-1-基)铵、苄基三甲基铵、苄基三乙基铵,此外还有离子,锍离子,优选三(C1-C4烷基)锍,如三甲基锍,以及氧化锍离子,优选三(C1-C4烷基)氧化锍。
还可以与上述可农用阳离子的盐的形式使用式I的活性化合物和至少一种选自如下的除草剂B:炔禾灵、炔草酯、氯丁草、氰氟草酯、氯甲草、唑禾草灵、高唑禾草灵、噻唑禾草灵、吡氟禾草灵、精吡氟禾草灵、吡氟氯禾灵、精吡氟氯禾灵、恶草醚、喔草酯、喹禾灵、精喹禾灵、三氟苯氧丙酸、枯杀达、丁氧环酮、烯草酮、环己烯草酮、噻草酮、环苯草酮、稀禾定、醌肟草、肟草酮、磺氨黄隆、四唑黄隆、苄嘧黄隆、氯嘧黄隆、绿黄隆、醚黄隆、环丙黄隆、胺苯黄隆、乙氧嘧黄隆、啶嘧黄隆、氟啶黄隆、甲酰胺黄隆、吡氯黄隆、啶咪黄隆、碘黄隆、甲基二黄隆、甲黄隆、烟黄隆、环丙氧黄隆、氟嘧黄隆、氟丙黄隆、吡嘧黄隆、玉嘧黄隆、嘧黄隆、乙黄黄隆、噻黄隆、醚苯黄隆、苯黄隆、三氟啶黄隆、氟胺磺隆、三氟甲磺隆、丙苯磺隆、氟酮黄隆、咪草酯、咪草啶酸、甲基咪草烟、灭草烟、灭草喹、咪草烟、唑嘧磺胺盐、唑嘧磺胺、双氟磺草胺、氟唑啶草、唑草磺胺、五氟磺草胺、双嘧苯甲酸、嘧硫苯甲酸、flucetosulfuron、orthosulfamuron、pyrimisulfam、[N-(5,7-二甲氧基[1,2,4]三唑并[1,5-a]-嘧啶-2-基-2-甲氧基-4-(三氟甲基)-3-吡啶磺酰胺、肟啶草、噻草平、氟锁草醚、氯氟草醚、乙羧氟草醚、氟黄胺草醚、氟硝磺酰胺、乳氟禾草灵、氟唑草、酰亚胺苯氧乙酸、达草氟、氟酮唑草、flufenpyr、硝磺酮、磺草酮、topramezone、4-羟基-3-{[2-甲基-6-(三氟甲基)-3-吡啶基]羰基}双环[3.2.1]辛-3-烯-2-酮、4-羟基-3-{[2-(2-甲氧基乙氧基)甲基-6-(三氟甲基)-3-吡啶基]羰基}双环[3.2.1]辛-3-烯-2-酮、4-羟基-3-[4-(甲基磺酰基)-2-硝基苯甲酰基]双环[3.2.1]辛-3-烯-2-酮、2-[2-氯-4-(甲基磺酰基)-3-[(2,2,2-三氟乙氧基)甲基]苯甲酰基]-3-羟基-2-环己烯-1-酮、pyrasulfotole、草甘膦、草铵膦、双丙氨酰膦、稗草胺、2,4-滴、2,4-滴丁酸、2,4-滴丙酸、高2,4-滴丙酸、2甲4氯、2甲4氯丁酸、2甲4氯丙酸、高2甲4氯丙酸、2,4,5-涕、草灭平、麦草畏、草芽平、杀草畏、二氯喹啉酸、喹草酸、二氯皮考啉酸、氟草烟、毒莠定、定草酯、aminopyralid、抑草生、二氟吡隆、喹氧乙酸、解草唑、双苯唑酸和吡咯二酸。
有用酸加成盐的阴离子主要是氯离子、溴离子、氟离子、碘离子、硫酸氢根、甲基硫酸根、硫酸根、磷酸二氢根、磷酸氢根、硝酸根、碳酸氢根、碳酸根、六氟硅酸根、六氟磷酸根、苯甲酸根和C1-C4链烷酸的阴离子,优选甲酸根、乙酸根、丙酸根和丁酸根。
根据本发明,除草剂莎草快、二乙除草双、苯敌快、敌草快阳离子、伐草快和对草快通常以与上述可农用阴离子的盐形式使用。
根据本发明,带有羧基的活性化合物也可以代替上述活性化合物以可农用衍生物形式使用,例如以酰胺如单-或二-C1-C6烷基酰胺或芳基酰胺、酯如烯丙基酯、炔丙基酯、C1-C10烷基酯或烷氧基烷基酯以及硫酯如C1-C10烷基硫酯使用。还可以衍生物使用的具有COOH基团的活性化合物实例是:炔禾灵、炔草酯、氯丁草、氰氟草酯、氯甲草、唑禾草灵、高唑禾草灵、噻唑禾草灵、吡氟禾草灵、精吡氟禾草灵、吡氟氯禾灵、精吡氟氯禾灵、恶草醚、喔草酯、喹禾灵、精喹禾灵、三氟苯氧丙酸、苄嘧黄隆、氯嘧黄隆、胺苯黄隆、氟啶黄隆、吡氯黄隆、碘黄隆、甲基二黄隆、甲黄隆、氟嘧黄隆、吡嘧黄隆、嘧黄隆、噻黄隆、苯黄隆、氟胺磺隆、咪草酯、咪草啶酸、甲基咪草烟、灭草烟、灭草喹、咪草烟、唑嘧磺胺盐、双嘧苯甲酸、嘧硫苯甲酸、肟啶草、氟锁草醚、氯氟草醚、乙羧氟草醚、乳氟禾草灵、氟唑草、酰亚胺苯氧乙酸、达草氟、氟酮唑草、flufenpyr、稗草胺、2,4-滴、2,4-滴丁酸、2,4-滴丙酸、高2,4-滴丙酸、2甲4氯、2甲4氯丁酸、2甲4氯丙酸、高2甲4氯丙酸、2,4,5-涕、草灭平、麦草畏、草芽平、杀草畏、二氯喹啉酸、喹草酸、二氯皮考啉酸、氟草烟、毒莠定、定草酯、aminopyralid、抑草生、二氟吡隆、喹氧乙酸、解草唑、双苯唑酸和吡咯二酸。
优选的单-和二-C1-C6烷基酰胺是甲基-和二甲基酰胺。优选的芳基酰胺例如为酰替苯胺和2-氯酰替苯胺。优选的烷基酯例如为甲基、乙基、丙基、异丙基、丁基、异丁基、戊基、mexyl(1-甲基己基)或异辛基(2-乙基己基)酯。优选的C1-C4烷氧基-C1-C4烷基酯是直链或支化的C1-C4烷氧基乙基酯,例如甲氧基乙基、乙氧基乙基或丁氧基乙基酯。直链或支化C1-C10烷基硫酯的实例是乙基硫酯。
根据本发明,在至少一种式I的3-苯基尿嘧啶作为活性化合物A与至少一种除草剂B组合和/或与至少一种安全剂C组合时使用二元和三元组合物。
这里和下文中的术语“二元组合物”包括包含一种或多种,例如2或3种活性化合物A和一种或多种,例如2或3种除草剂B或一种或多种,例如2或3种安全剂C的组合物。相应地,术语“三元组合物”包括包含一种或多种,例如2或3种活性化合物A、一种或多种,例如2或3种除草剂B和一种或多种,例如2或3种安全剂C的组合物。
在包含至少一种式I的3-苯基尿嘧啶作为组分A和至少一种除草剂B的二元组合物中,活性化合物的重量比A∶B通常为1∶500-10∶1,优选1∶100-10∶1,尤其是1∶50-10∶1,特别优选1∶25-5∶1。
在包含至少一种式I的3-苯基尿嘧啶和至少一种安全剂C的二元组合物中,活性化合物的重量比A∶C通常为1∶100-10∶1,优选1∶50-10∶1,尤其是1∶25-5∶1。
在包含3-苯基尿嘧啶I作为组分A、至少一种除草剂B和至少一种安全剂C的三元组合物中,各组分的相对重量比A∶B∶C通常为10∶1∶1-1∶500∶10,优选10∶1∶1-1∶100∶10,尤其是10∶1∶1-1∶50∶1,特别优选5∶1∶1-1∶25∶5。在这些三元组合物中,除草剂B与安全剂C的重量比优选为50∶1-1∶10。
在本发明的特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b1)组除草活性化合物,特别是选自炔草酯、氯甲草、唑禾草灵、高唑禾草灵、环苯草酮、稀禾定、醌肟草、pinoxaden和肟草酮的b1)组除草活性化合物以及需要的话安全剂C),尤其是选自解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b2)组除草活性化合物,特别是选自磺氨黄隆、绿黄隆、甲酰胺黄隆、碘黄隆、甲基二黄隆、甲黄隆、烟黄隆、氟嘧黄隆、氟丙黄隆、玉嘧黄隆、乙黄黄隆、三氟甲磺隆、丙苯磺隆、氟酮黄隆、咪草酯、咪草啶酸、甲基咪草烟、灭草烟、灭草喹、咪草烟、唑草磺胺、唑嘧磺胺、双氟磺草胺、五氟磺草胺、环酯草醚、[N-(5,7-二甲氧基[1,2,4]三唑并[1,5-a]嘧啶-2-基-2-甲氧基-4-(三氟甲基)-3-吡啶磺酰胺和肟啶草的b2)组除草活性化合物以及需要的话安全剂C),尤其是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b3)组除草活性化合物,特别是选自莠去津、草净津、特丁津、氨唑草酮、绿麦隆、敌草隆、异丙隆、噻唑隆、敌稗、溴苯腈、碘苯腈和对草快的b3)组除草活性化合物以及需要的话安全剂C),尤其是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b5)组除草活性化合物,特别是选自吡氟草胺、氟吡酰草胺、硝磺酮、磺草酮、异氟草、4-(3-三氟甲基苯氧基)-2-(4-三氟甲基苯基)嘧啶、topramezone、4-羟基-3-{[2-甲基-6-(三氟甲基)-3-吡啶基]羰基}双环[3.2.1]辛-3-烯-2-酮、4-羟基-3-{[2-(2-甲氧基乙氧基)甲基-6-(三氟甲基)-3-吡啶基]羰基}双环[3.2.1]辛-3-烯-2-酮、4-羟基-3-[4-(甲基磺酰基)-2-硝基苯甲酰基]双环[3.2.1]-辛-3-烯-2-酮、2-[2-氯-4-(甲基磺酰基)-3-[(2,2,2-三氟乙氧基)甲基]苯甲酰基]-3-羟基-2-环己烯-1-酮、pyrasulfotole的b5)组除草活性化合物以及需要的话安全剂C),尤其是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b6)组除草活性化合物,特别是草甘膦以及需要的话安全剂C),尤其是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b7)组除草活性化合物,特别是草铵膦以及需要的话安全剂C),尤其是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b9)组除草活性化合物,特别是胺硝草以及需要的话安全剂C),尤其是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b10)组除草活性化合物,特别是选自乙草胺、丁草胺、噻吩草胺、精噻吩草胺、异丙甲草胺、S-异丙甲草胺、烯草胺、丙草胺、氟噻草胺、苯噻草胺和四唑草胺的b10)组除草活性化合物以及需要的话安全剂C),尤其是选自2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷、抑害胺、解草呋、解草腈、肟草安、解草酮、解草啶和4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b13)组除草活性化合物,特别是选自2,4-滴、2,4-滴丙酸、高2,4-滴丙酸、2甲4氯丙酸、2甲4氯、高2甲4氯丙酸、麦草畏、二氯喹啉酸和喹草酸的b13)组除草活性化合物以及需要的话安全剂C),尤其是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b14)组除草活性化合物,特别是二氟吡隆以及需要的话安全剂C),尤其是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种b15)组除草活性化合物,特别是选自环庚草醚、氯嗪草和苯氧丙胺津的b15)组除草活性化合物以及需要的话安全剂C),尤其是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种选自灭草烟、咪草烟、咪草啶酸、甲基咪草烟、灭草喹、氯嘧黄隆、氟唑啶草、喹禾灵、精喹禾灵、吡氟禾草灵、精吡氟禾草灵、唑禾草灵、高唑禾草灵、枯杀达、稀禾定、烯草酮、噻草酮、醌肟草及其可农用盐和衍生物的除草剂B组合并任选与至少一种安全剂组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。更优选除草剂选自咪草烟或咪草啶酸。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种安全剂C),特别是选自解草呋、解草唑、喹氧乙酸、双苯唑酸和吡咯二酸的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
在本发明的另一特别优选实施方案中,优选包含与至少一种,尤其准确的是一种安全剂C),特别是选自2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷、抑害胺、解草呋、解草腈、肟草安、解草酮、解草啶和4-(二氯乙酰基)-1-氧杂4-氮杂螺[4.5]癸烷的安全剂C)组合的式I的3-苯基尿嘧啶,尤其是式Ia或Ib的3-苯基尿嘧啶的那些本发明组合物。
根据最优选的实施方案,将式I的3-苯基尿嘧啶与草甘膦组合并任选与选自解草酮、喹氧乙酸、抑害腈、抑害胺、dicyclonon、dietholate、解草唑、解草啶、解草安、肟草安、解草呋、双苯唑酸、吡咯二酸、mephenate、萘二甲酐、2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷(R-29148)、4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷(AD-67、MON 4660)和解草腈的安全剂C组合使用,所述安全剂包括它们的可农用盐以及在它们具有羧基的情况下还包括其可农用衍生物。
根据另一最优选实施方案,将式I的3-苯基尿嘧啶与咪草烟组合并任选与选自解草酮、喹氧乙酸、抑害腈、抑害胺、dicyclonon、dietholate、解草唑、解草啶、解草安、肟草安、解草呋、双苯唑酸、吡咯二酸、mephenate、萘二甲酐、2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷(R-29148)、4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷(AD-67、MON 4660)和解草腈的安全剂C组合使用,所述安全剂包括它们的可农用盐以及在它们具有羧基的情况下还包括其可农用衍生物。
根据另一最优选实施方案,将式I的3-苯基尿嘧啶与噻吩草胺或精噻吩草胺组合并任选与选自解草酮、喹氧乙酸、抑害腈、抑害胺、dicyclonon、dietholate、解草唑、解草啶、解草安、肟草安、解草呋、双苯唑酸、吡咯二酸、mephenate、萘二甲酐、2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷(R-29148)、4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷(AD-67、MON 4660)和解草腈的安全剂C组合使用,所述安全剂包括它们的可农用盐以及在它们具有羧基的情况下还包括其可农用衍生物。
根据另一最优选实施方案,将式I的3-苯基尿嘧啶与草甘膦组合并任选与至少一种选自咪草烟、噻吩草胺和精噻吩草胺的其他除草剂B和任选至少一种安全剂C组合使用,所述安全剂包括它们的可农用盐以及在它们具有羧基的情况下还包括其可农用衍生物。
优选安全剂C选自解草酮、抑害胺、解草啶、肟草安、解草呋、萘二甲酐、2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷、4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷和解草腈。
特别优选例如作为活性化合物A)包含苯基尿嘧啶I.7且作为另一活性化合物包含表2的一行所列物质的那些组合物(组合物1.1-1.353)。组合物1.1-1.353中各组分的重量比例在所述限度内,例如在苯基尿嘧啶I.7和除草剂B)的二元混合物的情况下为1∶1、1∶2或1∶5,在苯基尿嘧啶I.7和安全剂C的二元混合物的情况下为1∶1、1∶2或1∶5且在苯基尿嘧啶I.7、除草剂B和安全剂C的三元混合物的情况下为1∶1∶1、2∶1∶1、1∶2∶1、1∶5∶1或1∶5∶2。
表2
组合物序号 | 除草剂B) | 安全剂C) |
1.1 | 炔草酯 | |
1.2 | 炔草酯 | 喹氧乙酸 |
1.3 | 炔草酯 | 解草唑 |
1.4 | 炔草酯 | 双苯唑酸 |
1.5 | 炔草酯 | 吡咯二酸 |
1.6 | 氰氟草酯 | |
1.7 | 氰氟草酯 | 喹氧乙酸 |
1.8 | 氰氟草酯 | 解草唑 |
1.9 | 氰氟草酯 | 双苯唑酸 |
1.10 | 氰氟草酯 | 吡咯二酸 |
1.11 | 氯甲草 | |
1.12 | 氯甲草 | 喹氧乙酸 |
1.13 | 氯甲草 | 解草唑 |
1.14 | 氯甲草 | 双苯唑酸 |
1.15 | 氯甲草 | 吡咯二酸 |
1.16 | 唑禾草灵 |
1.17 | 唑禾草灵 | 喹氧乙酸 |
1.18 | 唑禾草灵 | 解草唑 |
1.19 | 唑禾草灵 | 双苯唑酸 |
1.20 | 唑禾草灵 | 吡咯二酸 |
1.21 | 高唑禾草灵 | - |
1.22 | 高唑禾草灵 | 喹氧乙酸 |
1.23 | 高唑禾草灵 | 解草唑 |
1.24 | 高唑禾草灵 | 双苯唑酸 |
1.25 | 高唑禾草灵 | 吡咯二酸 |
1.26 | 吡氟禾草灵 | - |
1.27 | 吡氟禾草灵 | 喹氧乙酸 |
1.28 | 吡氟禾草灵 | 解草唑 |
1.29 | 吡氟禾草灵 | 双苯唑酸 |
1.30 | 吡氟禾草灵 | 吡咯二酸 |
1.31 | 精吡氟禾草灵 | - |
1.32 | 精吡氟禾草灵 | 喹氧乙酸 |
1.33 | 精吡氟禾草灵 | 解草唑 |
1.34 | 精吡氟禾草灵 | 双苯唑酸 |
1.35 | 精吡氟禾草灵 | 吡咯二酸 |
1.36 | 吡氟氯禾灵 | - |
1.37 | 吡氟氯禾灵 | 喹氧乙酸 |
1.38 | 吡氟氯禾灵 | 解草唑 |
1.39 | 吡氟氯禾灵 | 双苯唑酸 |
1.40 | 吡氟氯禾灵 | 吡咯二酸 |
1.41 | 精吡氟氯禾灵 | - |
1.42 | 精吡氟氯禾灵 | 喹氧乙酸 |
1.43 | 精吡氟氯禾灵 | 解草唑 |
1.44 | 精吡氟氯禾灵 | 双苯唑酸 |
1.45 | 精吡氟氯禾灵 | 吡咯二酸 |
1.46 | 喹禾灵 | - |
1.47 | 喹禾灵 | 喹氧乙酸 |
1.48 | 喹禾灵 | 解草唑 |
1.49 | 喹禾灵 | 双苯唑酸 |
1.50 | 喹禾灵 | 吡咯二酸 |
1.51 | 精喹禾灵 | - |
1.52 | 精喹禾灵 | 喹氧乙酸 |
1.53 | 精喹禾灵 | 解草唑 |
1.54 | 精喹禾灵 | 双苯唑酸 |
1.55 | 精喹禾灵 | 吡咯二酸 |
1.56 | 枯杀达 | - |
1.57 | 丁氧环酮 | - |
1.58 | 烯草酮 | - |
1.59 | 环己烯草酮 | - |
1.60 | 噻草酮 | - |
1.61 | 环苯草酮 | - |
1.62 | 稀禾定 | - |
1.63 | 醌肟草 | - |
1.64 | 肟草酮 | - |
1.65 | 磺氨黄隆 | - |
1.66 | 磺氨黄隆 | 喹氧乙酸 |
1.67 | 磺氨黄隆 | 解草唑 |
1.68 | 磺氨黄隆 | 双苯唑酸 |
1.69 | 磺氨黄隆 | 吡咯二酸 |
1.70 | 磺氨黄隆 | 解草呋 |
1.71 | 四唑黄隆 | - |
1.72 | 苄嘧黄隆 | - |
1.73 | 氯嘧黄隆 | - |
1.74 | 绿黄隆 | - |
1.75 | 醚黄隆 | - |
1.76 | 环丙黄隆 | - |
1.77 | 胺苯黄隆 | - |
1.78 | 乙氧嘧黄隆 | - |
1.79 | 啶嘧黄隆 | - |
1.80 | 氟啶黄隆 | - |
1.81 | 甲酰胺黄隆 | - |
1.82 | 甲酰胺黄隆 | 喹氧乙酸 |
1.83 | 甲酰胺黄隆 | 解草唑 |
1.84 | 甲酰胺黄隆 | 双苯唑酸 |
1.85 | 甲酰胺黄隆 | 吡咯二酸 |
1.86 | 甲酰胺黄隆 | 解草呋 |
1.87 | 吡氯黄隆 | - |
1.88 | 吡氯黄隆 | 喹氧乙酸 |
1.89 | 吡氯黄隆 | 解草唑 |
1.90 | 吡氯黄隆 | 双苯唑酸 |
1.91 | 吡氯黄隆 | 吡咯二酸 |
1.92 | 吡氯黄隆 | 解草呋 |
1.93 | 啶咪黄隆 | - |
1.94 | 碘黄隆 | - |
1.95 | 碘黄隆 | 喹氧乙酸 |
1.96 | 碘黄隆 | 解草唑 |
1.97 | 碘黄隆 | 双苯唑酸 |
1.98 | 碘黄隆 | 吡咯二酸 |
1.99 | 碘黄隆 | 解草呋 |
1.100 | 甲基二黄隆 | - |
1.101 | 甲基二黄隆 | 喹氧乙酸 |
1.102 | 甲基二黄隆 | 解草唑 |
1.103 | 甲基二黄隆 | 双苯唑酸 |
1.104 | 甲基二黄隆 | 吡咯二酸 |
1.105 | 甲基二黄隆 | 解草呋 |
1.106 | 甲黄隆 | - |
1.107 | 烟黄隆 | - |
1.108 | 环丙氧黄隆 | - |
1.109 | 氟嘧黄隆 | - |
1.110 | 氟丙黄隆 | - |
1.111 | 吡嘧黄隆 | - |
1.112 | 玉嘧黄隆 | - |
1.113 | 嘧黄隆 | - |
1.114 | 乙黄黄隆 | - |
1.115 | 噻黄隆 | - |
1.116 | 醚苯黄隆 | - |
1.117 | 苯黄隆 | - |
1.118 | 三氟啶黄隆 | - |
1.119 | 氟胺磺隆 | - |
1.120 | 三氟甲磺隆 | - |
1.121 | 丙苯磺隆 | - |
1.122 | 氟酮黄隆 | - |
1.123 | 咪草酯 | - |
1.124 | 咪草啶酸 | - |
1.125 | 甲基咪草烟 | - |
1.126 | 灭草烟 | - |
1.127 | 灭草喹 | - |
1.128 | 咪草烟 | - |
1.129 | 唑嘧磺胺盐 | - |
1.130 | 唑嘧磺胺 | - |
1.131 | 双氟磺草胺 | - |
1.132 | 氟唑啶草 | - |
1.133 | 唑草磺胺 | - |
1.134 | 五氟磺草胺 | - |
1.135 | 双嘧苯甲酸 | - |
1.136 | 嘧苯草肟 | - |
1.137 | 环酯草醚 | - |
1.138 | 嘧硫苯甲酸 | - |
1.139 | 肟啶草 | - |
1.140 | 莠去津 | - |
1.141 | 草净津 | - |
1.142 | 西玛津 | - |
1.143 | 特丁津 | - |
1.144 | 六嗪同 | - |
1.145 | 苯嗪草 | - |
1.146 | 赛克津 | - |
1.147 | 氨唑草酮 | - |
1.148 | 杀草敏 | - |
1.149 | 氯溴隆 | - |
1.150 | 绿麦隆 | - |
1.151 | 敌草隆 | - |
1.152 | 异丙隆 | - |
1.153 | 利谷隆 | - |
1.154 | 噻唑隆 | - |
1.155 | 敌稗 | - |
1.156 | 溴苯腈 | - |
1.157 | 碘苯腈 | - |
1.158 | 噻草平 | - |
1.159 | 达草止 | - |
1.160 | 苯敌快 | - |
1.161 | 敌草快阳离子 | - |
1.162 | 对草快 | - |
1.163 | 氟锁草醚 | - |
1.164 | 乙羧氟草醚 | - |
1.165 | 氟硝磺酰胺 | - |
1.166 | 乳氟禾草灵 | - |
1.167 | 氟硝草醚 | - |
1.168 | 异丙吡草酯 | - |
1.169 | 氟唑草 | - |
1.170 | 吲哚酮草酯 | - |
1.171 | 酰亚胺苯氧乙酸 | - |
1.172 | 氟嗪酮 | - |
1.173 | 达草氟 | - |
1.174 | 恶草灵 | - |
1.175 | 炔丙唑草 | - |
1.176 | 唑啶炔草 | - |
1.177 | 氟酮唑草 | - |
1.178 | 磺胺草唑 | - |
1.179 | 戊唑草 | - |
1.180 | 双苯嘧草酮 | - |
1.181 | 氟丙嘧草酯 | - |
1.182 | 双唑草腈 | - |
1.183 | 氟唑草胺 | - |
1.184 | flufenpyr | - |
1.185 | 吡氯草胺 | - |
1.186 | 达草灭 | - |
1.187 | 吡氟草胺 | - |
1.188 | 氟吡酰草胺 | - |
1.189 | 氟丁酰草胺 | - |
1.190 | 氟草同 | - |
1.191 | 氟咯草酮 | - |
1.192 | 呋草酮 | - |
1.193 | 硝磺酮 | - |
1.194 | 磺草酮 | - |
1.195 | 氯草酮 | - |
1.196 | 异氟草 | - |
1.197 | 吡草酮 | - |
1.198 | 吡唑特 | - |
1.199 | 苄草唑 | - |
1.200 | 苯并双环酮 | - |
1.201 | 异恶草酮 | - |
1.202 | pinoxaden | - |
1.203 | flucetosulfuron | - |
1.204 | orthosulfanuron | - |
1.205 | pyrimisulfan | - |
1.206 | 草甘膦 | - |
1.207 | 草铵膦 | - |
1.208 | 氟草胺 | - |
1.209 | 地乐胺 | - |
1.210 | 敌乐胺 | - |
1.211 | 丁氟消草 | - |
1.212 | 黄草消 | - |
1.213 | 胺硝草 | - |
1.214 | 氟乐灵 | - |
1.215 | 拿草特 | - |
1.216 | 乙草胺 | - |
1.217 | 乙草胺 | 抑害胺 |
1.218 | 乙草胺 | 解草呋 |
1.219 | 乙草胺 | 解草腈 |
1.220 | 乙草胺 | 肟草安 |
1.221 | 乙草胺 | 解草酮 |
1.222 | 乙草胺 | 解草啶 |
1.223 | 甲草胺 | - |
1.224 | 丁草胺 | - |
1.225 | 丁草胺 | 抑害胺 |
1.226 | 丁草胺 | 解草呋 |
1.227 | 丁草胺 | 解草腈 |
1.228 | 丁草胺 | 肟草安 |
1.229 | 丁草胺 | 解草酮 |
1.230 | 丁草胺 | 解草啶 |
1.231 | 噻吩草胺 | - |
1.232 | 噻吩草胺 | 抑害胺 |
1.233 | 噻吩草胺 | 解草呋 |
1.234 | 噻吩草胺 | 解草腈 |
1.235 | 噻吩草胺 | 肟草安 |
1.236 | 噻吩草胺 | 解草酮 |
1.237 | 噻吩草胺 | 解草啶 |
1.238 | 精噻吩草胺 | - |
1.239 | 精噻吩草胺 | 抑害胺 |
1.240 | 精噻吩草胺 | 解草呋 |
1.241 | 精噻吩草胺 | 解草腈 |
1.242 | 精噻吩草胺 | 肟草安 |
1.243 | 精噻吩草胺 | 解草酮 |
1.244 | 精噻吩草胺 | 解草啶 |
1.245 | 吡草胺 | - |
1.246 | 异丙甲草胺 | - |
1.247 | 异丙甲草胺 | 抑害胺 |
1.248 | 异丙甲草胺 | 解草呋 |
1.249 | 异丙甲草胺 | 解草腈 |
1.250 | 异丙甲草胺 | 肟草安 |
1.251 | 异丙甲草胺 | 解草酮 |
1.252 | 异丙甲草胺 | 解草啶 |
1.253 | S-异丙甲草胺 | - |
1.254 | S-异丙甲草胺 | 抑害胺 |
1.255 | S-异丙甲草胺 | 解草呋 |
1.256 | S-异丙甲草胺 | 解草腈 |
1.257 | S-异丙甲草胺 | 肟草安 |
1.258 | S-异丙甲草胺 | 解草酮 |
1.259 | S-异丙甲草胺 | 解草啶 |
1.260 | 烯草胺 | - |
1.261 | 丙草胺 | - |
1.262 | 丙草胺 | 抑害胺 |
1.263 | 丙草胺 | 解草呋 |
1.264 | 丙草胺 | 解草腈 |
1.265 | 丙草胺 | 肟草安 |
1.266 | 丙草胺 | 解草酮 |
1.267 | 丙草胺 | 解草啶 |
1.268 | 唑草胺 | - |
1.269 | 毒草安 | - |
1.270 | 异丙草胺 | - |
1.271 | 噻醚草胺 | - |
1.272 | 氟噻草胺 | - |
1.273 | 苯噻草胺 | - |
1.274 | 四唑草胺 | - |
1.275 | 唑草胺 | - |
1.276 | 茚草酮 | - |
1.277 | 敌草腈 | - |
1.278 | 草克乐 | - |
1.279 | 异恶草胺 | - |
1.280 | 2,4-滴 | - |
1.281 | 2,4-滴丁酸 | - |
1.282 | 2,4-滴丙酸 | - |
1.283 | 高2,4-滴丙酸 | - |
1.284 | 2甲4氯 | - |
1.285 | 2甲4氯丁酸 | - |
1.286 | 2甲4氯丙酸 | - |
1.287 | 高2甲4氯丙酸 | - |
1.288 | 麦草畏 | - |
1.289 | 二氯喹啉酸 | - |
1.290 | 喹草酸 | - |
1.291 | 二氯皮考啉酸 | - |
1.292 | 氟草烟 | - |
1.293 | 毒莠定 | - |
1.294 | 定草酯 | - |
1.295 | 草除灵 | - |
1.296 | 二氟吡隆 | - |
1.297 | 溴丁酰草胺 | - |
1.298 | 环庚草醚 | - |
1.299 | 苯丙隆 | - |
1.300 | 氯嗪草 | - |
1.301 | 苯氧丙胺津 | - |
1.302 | - | 解草酮 |
1.303 | - | 喹氧乙酸 |
1.304 | - | 抑害腈 |
1.305 | - | 抑害胺 |
1.306 | - | dicyclonon |
1.307 | - | dietholate |
1.308 | - | 解草唑 |
1.309 | - | 解草啶 |
1.310 | - | 解草安 |
1.311 | - | 肟草安 |
1.312 | - | 解草呋 |
1.313 | - | 双苯唑酸 |
1.314 | - | 吡咯二酸 |
1.315 | - | mephenate |
1.316 | - | 萘二甲酐 |
1.317 | - | 解草腈 |
1.318 | - | 2,2,5-三甲基-3-(二氯乙酰基)唑烷 |
1.319 | 4-(3-三氟甲基苯氧基)-2-(4-三氟甲基苯基)嘧啶 | - |
1.320 | 乙草胺 | 2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷 |
1.321 | 丁草胺 | 2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷 |
1.322 | 噻吩草胺 | 2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷 |
1.323 | 精噻吩草胺 | 2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷 |
1.324 | 异丙甲草胺 | 2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷 |
1.325 | S-异丙甲草胺 | 2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷 |
1.326 | 丙草胺 | 2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷 |
1.327 | 烯草胺 | 2,2,5-三甲基-3-(二氯乙酰基)-1,3-唑烷 |
1.328 | 烯草胺 | 抑害胺 |
1.329 | 烯草胺 | 解草呋 |
1.330 | 烯草胺 | 解草腈 |
1.331 | 烯草胺 | 肟草安 |
1.332 | 烯草胺 | 解草酮 |
1.333 | 烯草胺 | 解草啶 |
1.334 | 烯草胺 | 4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷 |
1.335 | 乙草胺 | 4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷 |
1.336 | 丁草胺 | 4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷 |
1.337 | 噻吩草胺 | 4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷 |
1.338 | 精噻吩草胺 | 4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷 |
1.339 | 异丙甲草胺 | 4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷 |
1.340 | S-异丙甲草胺 | 4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷 |
1.341 | 丙草胺 | 4-(二氯乙酰基)-1-氧杂-4-氮杂螺[4.5]癸烷 |
1.342 | 唑酰草胺 | - |
1.343 | 唑酰草胺 | 喹氧乙酸 |
1.344 | 唑酰草胺 | 解草唑 |
1.345 | 唑酰草胺 | 双苯唑酸 |
1.346 | 唑酰草胺 | 吡咯二酸 |
1.347 | topramezone | - |
1.348 | bencarbozone | - |
1.349 | 4-羟基-3-{[2-甲基-6-(三氟甲基)-3-吡啶基]羰基}双环[3.2.1]辛-3-烯-2-酮 | - |
1.350 | 4-羟基-3-{[2-(2-甲氧基乙氧基)甲基-6-(三氟甲基)-3-吡啶基]羰基}双环[3.2.1]辛-3-烯-2-酮 | - |
1.351 | 4-羟基-3-[4-(甲基磺酰基)-2-硝基苯甲酰基]双环[3.2.1]-辛-3-烯-2-酮 | - |
1.352 | 2-[2-氯-4-(甲基磺酰基)-3-[(2,2,2-三氟乙氧基)甲基]苯甲酰基]-3-羟基-2-环己烯-1-酮 | - |
1.353 | pyrasulfotole | - |
若表2中提到的活性化合物具有可以被离子化的官能基团,则它们还可以其上述可农用盐形式存在。若表2中所提到的活性化合物具有羧基,则它们还可以其上述可农用衍生物形式存在。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.1替代的组合物2.1-2.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.2替代的组合物3.1-3.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.3替代的组合物4.1-4.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.4替代的组合物5.1-5.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.5替代的组合物6.1-6.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.6替代的组合物7.1-7.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.8替代的组合物8.1-8.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.9替代的组合物9.1-9.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.10替代的组合物10.1-10.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.11替代的组合物11.1-11.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.12替代的组合物12.1-12.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.13替代的组合物13.1-13.353。
还优选与对应组合物1.1-1.353的不同仅在于苯基尿嘧啶I.7被苯基尿嘧啶I.14-I.74替代的组合物14.1-74.353。
组合物2.1-74.353中各组分的重量比在上述限度内,例如在苯基尿嘧啶I.1和除草剂B)的二元混合物情况下为1∶1、1∶2或1∶5,在苯基尿嘧啶I.1和安全剂C的二元混合物情况下为1∶1、1∶2或1∶5且在苯基尿嘧啶I.1、除草剂B和安全剂C的三元混合物情况下为1∶1∶1、2∶1∶1、1∶2∶1、1∶5∶1或1∶5∶2。
对于施用而言,可以使用作物保护产品形式的即用制剂。组分A、任选的组分B和/或任选的组分C可以悬浮、乳化或溶解形式存在且可以联合或分开配制。施用形式完全取决于意欲的用途。
制剂例如可以借助喷雾、雾化、撒粉、撒播或浇灌而以可直接喷雾水溶液、粉末、悬浮液、高度浓缩的水性、油性或其他悬浮液或分散体、乳液、油分散体、糊、粉剂、撒播用材料或颗粒形式施用。使用形式取决于意欲的用途;在任何情况下它们应确保活性化合物的最佳可能分布。
取决于其中即用制剂存在的形式,它们包含一种或多种液体或固体载体,合适的话还有表面活性剂以及合适的话还有常用于配制作物保护产品的其他助剂。本领域熟练技术人员完全熟知该类配制剂的配方。
即用制剂可以包含常用于配制作物保护产品的助剂,这些助剂还可以包含液体载体。
具有载体功能的合适惰性添加剂主要是:中沸点到高沸点的矿物油馏分,如煤油和柴油,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,例如石蜡、四氢化萘、烷基化萘及其衍生物、烷基化苯及其衍生物,醇如甲醇、乙醇、丙醇、丁醇和环己醇,酮类如环己酮,强极性溶剂,例如胺类,如N-甲基吡咯烷酮,以及水。
含水使用形式可通过加入水由乳油、悬浮液、糊、可湿性粉末或水分散性颗粒制备。为制备乳液、糊或油分散体,可借助湿润剂、增粘剂、分散剂或乳化剂将活性化合物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需要的话溶剂或油组成的浓缩物且这些浓缩物适于用水稀释。
合适的表面活性剂是芳族磺酸如木素磺酸、苯酚磺酸、萘磺酸和二丁基萘磺酸以及脂肪酸、烷基-和烷基芳基磺酸、烷基硫酸、月桂基醚硫酸和脂肪醇硫酸的碱金属盐、碱土金属盐和铵盐,硫酸化十六-、十七-和十八烷醇以及脂肪醇乙二醇醚的盐,磺化萘及其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、辛基酚或壬基酚,烷基苯基聚乙二醇醚,三丁基苯基聚乙二醇醚,烷基芳基聚醚醇,异十三烷醇,脂肪醇/氧化乙烯缩合物,乙氧基化蓖麻油,聚氧乙烯烷基醚或聚氧丙烯烷基醚,月桂醇聚乙二醇醚乙酸酯,山梨醇酯,木素亚硫酸盐废液和甲基纤维素。
粉末、撒播用材料和粉剂可以通过将活性物质与固体载体混合或一起研磨来制备。
颗粒如包衣颗粒、浸渍颗粒和均质颗粒可以通过使活性成分与固体载体粘附而制备。固体载体为矿土如硅石、硅胶、硅酸盐、滑石、高岭土、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、脲类以及植物来源的产品如谷粉、树皮粉、木粉和坚果壳粉,纤维素粉或其它固体载体。
活性化合物在即用制剂中的浓度可以在宽范围内变化。配制剂通常包含0.001-98重量%,优选0.01-95重量%活性成分。活性成分以90-100%,优选95-100%的纯度(根据NMR光谱)使用。
制剂例如可以按如下配制:
I.将20重量份所述活性化合物溶于由80重量份烷基化苯、10重量份的8-10mol氧化乙烯与1mol油酸N-单乙醇酰胺的加合物、5重量份十二烷基苯磺酸钙和5重量份的40mol氧化乙烯与1mol蓖麻油的加合物组成的组合物中。将该溶液倾入100,000重量份水中并在其中精细分散,得到包含0.02重量%活性成分的水分散体。
II.将20重量份所述活性化合物溶于由40重量份环己酮、30重量份异丁醇、20重量份的7mol氧化乙烯与1mol异辛基苯酚的加合物和10重量份的40mol氧化乙烯与1mol蓖麻油的加合物组成的组合物中。将该溶液倾入100,000重量份水中并在其中精细分散,得到包含0.02重量%活性成分的水分散体。
III.将20重量份所述活性化合物溶于由25重量份环己酮、65重量份沸点为210-280℃的矿物油馏分和10重量份的40mol氧化乙烯与1mol蓖麻油的加合物组成的组合物中。将该溶液倾入100,000重量份水中并在其中精细分散,得到包含0.02重量%活性成分的水分散体。
IV.将20重量份所述活性化合物与3重量份二异丁基萘磺酸钠、17重量份来自亚硫酸盐废液的木素磺酸钠和60重量份粉状硅胶彻底混合并将组合物在锤磨机中研磨。将该组合物精细分散于20,000重量份水中,得到包含0.1重量%活性成分的喷雾组合物。
V.将3重量份所述活性化合物与97重量份细碎高岭土混合。得到包含3重量%活性成分的粉剂。
VI.将20重量份所述活性化合物与2重量份十二烷基苯磺酸钙、8重量份脂肪醇聚乙二醇醚、2重量份苯酚-脲-甲醛缩合物的钠盐和68重量份链烷烃矿物油均匀混合。得到稳定的油性分散体。
VII.将1重量份所述活性化合物溶于由70重量份环己酮、20重量份乙氧基化异辛基苯酚和10重量份乙氧基化蓖麻油组成的组合物中。得到稳定的乳油。
VIII.将1重量份所述活性化合物溶于由80重量份环己酮和20重量份Wettol EM 31(=基于乙氧基化蓖麻油的非离子乳化剂)组成的组合物中。得到稳定的乳油。
组分A、B和C可以联合或分开配制
组分A、B和C可以联合或分开、同时或依次、在植物出苗之前、之中或之后施用。
若活性化合物不能被某些作物植株良好地耐受,则可以使用其中借助喷雾器喷雾除草组合物以使敏感作物植株的叶子尽可能不受影响,而活性化合物到达生长在下面的不希望的植物的叶子或裸露的土壤表面的施用方法(后引导,最后耕作程序)。
任选与B组合和/或任选与C组合而不含配制助剂的纯活性化合物,即A的所需施用率取决于不希望的植物生长的密度、植物的发育阶段、使用组合物的场所的气候条件和施用方法。施用率通常为0.001-3kg/ha,优选0.005-2kg/ha,尤其是0.01-1kg/ha,0.1g/ha-1kg/ha,1-500g/ha或5-500g/ha活性物质。
主要通过喷雾,尤其是叶面喷雾将制剂施用于植物上。施用可以通过例如使用水作为载体并使用约50-1000l/ha(例如300-400l/ha)的喷雾液比率的常规喷雾技术进行。低容量和超低容量法施用制剂也是可能的,正如在以微颗粒形式施用一样。
在本发明的优选实施方案中,以对抗草甘膦杂草或作物提供防治的施用率施用式I的苯基尿嘧啶或活性成分的组合物,尤其在抗草甘膦杂草或作物出苗后,但优选在所需作物种植、播种或出苗之前施用。
在本发明的另一优选实施方案中,通过在所需作物播种、种植或出苗之前(出苗前或种植前施用)施用式I的苯基尿嘧啶或活性成分的组合物,然后在作物出苗后用一种或多种在该作物中具有选择性的除草剂进行一次或多次处理而提供对抗草甘膦杂草或作物的防治。
此外,可能有用的是以与其他作物保护产品如杀虫剂或防治植物病原性真菌或细菌的试剂的混合物联合施用本发明组合物。还令人感兴趣的是与用于治疗营养和痕量元素缺乏症的无机盐溶液的溶混性。还可以加入非植物毒性油和油浓缩物。
根据优选实施方案,本发明提供了在大豆、玉米或小粒禾谷类(例如小麦、大麦、燕麦)作物中对抗草甘膦杂草或作物的防治。
根据本发明的一个优选实施方案,提供了对构成天然侵染的一部分且耐受或抗常用施用率的草甘膦的杂草的防治。该类杂草的实例是飞蓬属(Erigeron)、蓬属(Conyza)、毒麦属(Lolium)、苋属(Amaranthus)、蟋蟀草属(Eleusine)、鸭跖草属(Commelina)、豚草属(Ambrosia)、苘麻属(Abutilon)、藜属(Chenopodium)或Didiptera属。
根据本发明的另一优选方面,防治抗草甘膦的“自生”作物,优选大豆、棉花、油菜、亚麻、扁豆、稻、糖用甜菜、向日葵、烟草、小麦或玉米作物。抗草甘膦作物包括借助多重基因组的改变(“堆叠特性(stacked trait)”)而呈现不止抗草甘膦的作物,如抗草甘膦和苯腈类(oxynil)的作物、抗草铵膦的作物、抗咪唑啉酮作物,抗磺酰脲作物,抗麦草畏作物,抗环己烷二酮作物,抗PPO作物,抗HPPD作物,抗真菌或昆虫的作物。在本发明的最优选实施方案中,被防治的“自生”作物为大豆作物。在本发明的另一最优选实施方案中,被防治的“自生”作物为玉米作物。在本发明的另一最优选实施方案中,被防治的“自生”作物为棉花作物。在本发明的另一最优选实施方案中,被防治的“自生”作物为油菜作物。
抗性可以通过基因工程赋予“自生”作物。例如,通过所述技术,该类作物可能获得合成如下物质的能力:(i)一种或多种选择性作用的毒素,尤其是杀真菌毒素或杀虫毒素,如由产生毒素的细菌已知的那些,尤其是芽孢杆菌属的那些,例如内毒素,如CryIA(b)、CryIA(c)、CryIF、CryIF(a2)、CryIIA(b)、CryIIIA、CryIIIB(b1)、Cry9c、VIP1、VIP2、VIP3或VIP3A或杂化物(即该类毒素的不同畴的组合)、改性物(通过对天然序列中的一种或多种氨基酸的替换,例如CryIIIA055)和/或其截断形式,和/或(ii)改变为除草剂的目标的酶的量,和/或(iii)为除草剂的目标的酶的改性形式,和/或(iv)一种或多种单独或一起能够将除草剂转化成对植物没有毒性的化学产品的酶和/或(v)抗病原性物质,如所谓的“致病性相关的蛋白”。该类作物由下表所述实例说明,但不限于此,这些实例可以市购或为本领域熟练技术人员所已知或者描述于引用的出版物中,该类作物还可以由表3所列特性中的不止一种堆叠而得到的其他任何实例说明。
表3
作物 | 抗性基因,事件,编码或注册商标 | 抗性 | 参考文献(见表底) |
大豆 | GTS-40-3-2 | 抗草甘膦作物 | 1) |
大豆 | Roundup Ready | 抗草甘膦作物 | 3) |
大豆 | CP4-EPSPS | 抗草甘膦作物 | 3) |
大豆 | GU262 | 抗草铵膦作物 | 1) |
大豆 | W62 | 抗草铵膦作物 | 1) |
大豆 | W98 | 抗草铵膦作物 | 1) |
棉花 | MON1445/1698 | 抗草甘膦作物 | 1) |
棉花 | WideStrike | 抗草甘膦和昆虫作物 | |
棉花 | Roundup Ready | 抗草甘膦作物 | 2) |
棉花 | Roundup ReadyFlex | 抗草甘膦作物 | |
棉花 | Roundup ReadyFlex+BollgardII | 抗草甘膦和昆虫作物 | |
棉花 | Roundup Ready+BollgardI | 抗草甘膦和昆虫作物 | |
棉花 | Roundup Ready+BollgardII | 抗草甘膦和昆虫作物 | |
棉花 | CP4-EPSPS | 抗草甘膦作物 | 3) |
油菜 | GT200 | 抗草甘膦作物 | 1) |
油菜 | GT73 | 抗草甘膦作物 | 1) |
油菜 | RT73 | 抗草甘膦作物 | 1) |
糖用甜菜 | GTSB77 | 抗草甘膦作物 | 1) |
糖用甜菜 | H7-1 | 抗草甘膦作物 | 1) |
糖用甜菜 | Roundup Ready | 抗草甘膦作物 | 3) |
糖用甜菜 | CP4-EPSPS | 抗草甘膦作物 | 3) |
糖用甜菜 | T120-7 | 抗草铵膦作物 | 1) |
小麦 | MON71800 | 抗草甘膦作物 | 1) |
玉米 | GA21 | 抗草甘膦作物 | 1),3) |
玉米 | MON802 | 抗昆虫和草甘膦作物 | 1) |
玉米 | MON809 | 抗昆虫和草甘膦作物 | 1) |
玉米 | MON832 | 抗草甘膦作物 | 1) |
玉米 | NK603 | 抗草甘膦作物 | 1) |
玉米 | NK 603x MON 810 | 抗昆虫和草甘膦作物 | 2) |
玉米 | Roundup Ready | 抗草甘膦作物 | 3) |
玉米 | Roundup Ready+YieldGard | 抗草甘膦和昆虫作物 |
作物 | 抗性基因,事件,编码或注册商标 | 抗性 | 参考文献(见表底) |
玉米螟 | |||
玉米 | Roundup Ready+YieldGard根虫 | 抗草甘膦和昆虫作物 | |
玉米 | CP4-EPSPS | 抗草甘膦作物 | 3) |
1)http://www.agbios.com/dbase.php#
2)WO 05/13696
3)G.Dill,Pest Manag.Sci.2005,61,219-224及其中所引用的参考文献;W.Pline-Srnic,Pest Manag.Sci.2005,61,225-234及其中所引用的参考文献
4)M.Matringe,A.Sailland,B.Pelissier,A.Rolland,O.Zink,Pest Manag.Sci,2005,61,269-276及其中所引用的参考文献;WO 96/38567;WO98/04685;WO 99/24585;WO 99/25842
在下列实施例中,使用S.R.Colby(1967)的方法[“计算除草剂组合的协同增效和拮抗响应”,Weeds 15,第22页及随后各页]计算各化合物的活性仅为加和时预期的E值。
E=X+Y-(XY/100)
其中
X=以施用率a使用活性化合物A时的效果(%);
Y=以施用率b使用活性化合物B时的效果(%);
E=A+B在施用率a+b下的预期效果(%)。
若试验测定的值高于根据Colby方程式计算的E值,则存在协同增效效果。
下列实施例说明本发明而不限制本发明。
实施例
使用本发明的苯基尿嘧啶I或其混合物对抗草甘膦杂草或作物的生长的效果通过田间和温室试验证实(实施例1-3)。
以合适的方式将本发明的苯基尿嘧啶I和/或其他活性成分分开或以混合物配制成例如乳油(EC)、可溶性浓缩物(SL)、悬浮乳液(SE)、悬浮浓缩物(SC)或水分散性颗粒(WG)。在紧临喷雾前将配制剂悬浮或乳化于作为分散介质的水中。然后借助精细分配喷嘴将含水混合物均匀喷雾于试验地块或植物地块上。
对于温室试验,使植物在盆中生长到3-6cm高,然后处理(出苗后)。在29天的试验期间中照料植物。
对于田间试验,试验地块具有均匀尺寸(通常各自为14-37m2)且已处理和未处理地块的分布根据无规则总体设计而组织。在对根据常规农业实践的区域和作物典型的季节成行播种抗草甘膦作物(棉花,实施例2;大豆,实施例3),或者它们作为自生作物偶然萌发(玉米,实施例3)。
对于种植前和种植前烧荒处理,在种植植物之前处理地块,典型的是在种植前7-28天进行处理。对于出苗前处理,在种植时(加或减2天)处理地块,但处理要在出苗前进行。对于出苗后或后引导处理,在杂草或作物出苗后处理地块。
由本发明的苯基尿嘧啶I和/或其他活性成分引起的损害的评价使用与未处理对照地块相比为0-100%的评分进行。这里0意味着没有损害,100意味着相应杂草或作物品种的植株完全毁坏。
实施例1-苯基尿嘧啶I.7单独以及苯基尿嘧啶I.7和草甘膦的混合物出苗后防治对草甘膦敏感和抗草甘膦的加拿大蓬;温室试验
结果示于下表4中。
表4
活性成分 | 施用率(g/ha) | 对草甘膦敏感的加拿大蓬(ERICA),第29天(除草剂防治%) | 抗草甘膦加拿大蓬(ERICA),第29天(除草剂防治%) |
草甘膦 | 420 | 98 | 0 |
苯基尿嘧啶I.7 | 6 | 100 | 100 |
草甘膦+苯基尿嘧啶I.7 | 420+6 | 100 | 100 |
在该实施例中,将草甘膦(异丙基铵盐)配制成353g/l SL并将苯基尿嘧啶I.7配制成120g/l EC。在施用之前,将配制的活性成分与187l/ha含水喷雾溶液桶混,该喷雾溶液此外含有15g/l硫酸铵和2.5g/l非离子表面活性剂。
实施例2-在后引导处理中苯基尿嘧啶I.7单独以及苯基尿嘧啶I.7和草甘膦的混合物防治抗草甘膦棉花;田间试验
结果示于下表5中。
表5
施用率(g/ha) | 抗草甘膦棉花,第3天(防治%) | ||
草甘膦 | 苯基尿嘧啶I.7 | 实测值 | 根据Colby方程的计算值 |
560 | - | 0 | - |
- | 25 | 38 | - |
560 | 25 | 80 | 38 |
在该实施例中,将草甘膦(异丙基铵盐)配制成480g/l SL并将苯基尿嘧啶I.7配制成120g/l EC。在施用之前,将配制的活性成分与140l/ha含水喷雾溶液桶混,该喷雾溶液此外含有2.5g/l非离子表面活性剂。抗草甘膦棉花在处理前77天种植。
实施例3-在抗草甘膦大豆中通过出苗前施用苯基尿嘧啶I.7和咪草烟的混合物防治自生抗草甘膦玉米;对于所需作物,即抗草甘膦大豆的出苗前处理;田间试验
结果示于下表6中。
表6
施用率(g/ha) | 防治抗草甘膦玉米,第29天(防治%) | 在抗草甘膦大豆中的植物毒性,第29天(损害%) | ||
苯基原嘧啶I.7 | 咪草烟 | 实测值 | 根据Colby方程的计算值 | |
25 | - | 0 | - | 0 |
- | 70 | 23 | - | 0 |
25 | 70 | 70 | 23 | 0 |
在该实施例中,将苯基尿嘧啶I.7配制成120g/l EC,并将咪草烟(铵盐)配制成240g/l SL。在施用之前,将配制的活性成分与187l/ha含水喷雾溶液桶混,该喷雾溶液此外含有20g/l硫酸铵和10g/l Agridex。在第7天种植大豆作物。
Claims (14)
1.一种防治抗草甘膦杂草或作物的方法,包括使除草有效量的一种或多种式I的3-苯基尿嘧啶或其可农用盐:
其中变量R1-R7如下所定义:
R1为甲基或NH2;
R2为C1-C2卤代烷基;
R3为氢或卤素;
R4为卤素或氰基;
R5为氢或C1-C6烷基;
R6、R7相互独立地为氢、C1-C6烷基、C1-C6烷氧基、C3-C6链烯基、C3-C6炔基、C3-C7环烷基、C3-C7环烯基、苯基或苄基;
作用于抗草甘膦杂草或作物或其生长场所。
2.根据权利要求1的方法,其中式I中的各变量R1-R7如下所定义:
R1为甲基或NH2;
R2为三氟甲基;
R3为氢、氟或氯;
R4为卤素或氰基;
R5为氢;
R6、R7相互独立地为氢、C1-C6烷基、C3-C6链烯基、C3-C6炔基、C3-C7环烷基、C3-C7环烯基、苯基或苄基。
3.根据权利要求1或2的方法,其中式I中的R6和R7为相同或不同的C1-C6烷基。
4.根据前述权利要求中任一项的方法,其中所述作物选自抗草甘膦的大豆、油菜、棉花、小麦和玉米。
5.根据前述权利要求中任一项的方法,其中使式I的3-苯基尿嘧啶与一种或多种其他除草剂B或其可农用盐组合使用。
6.根据权利要求5的方法,其中其他除草剂B选自下列b1)-b15)类除草剂或其可农用盐或衍生物(条件是该除草剂具有羧基):
b1)类脂生物合成抑制剂;
b2)乙酰乳酸酯合成酶抑制剂(ALS抑制剂);
b3)光合成抑制剂;
b4)原卟啉原-IX氧化酶抑制剂;
b5)白化除草剂;
b6)烯醇丙酮酰基莽草酸3-磷酸酯合成酶抑制剂(EPSP抑制剂);
b7)谷氨酰胺合成酶抑制剂;
b8)7,8-二氢蝶酸酯合成酶抑制剂(DHP抑制剂);
b9)有丝分裂抑制剂;
b11)长链脂肪酸合成抑制剂(VLCFA抑制剂);
b12)纤维素生物合成抑制剂;
b13)去偶除草剂;
b14)植物生长素输送抑制剂;
b15)选自新燕灵、氟燕灵、强氟燕灵、溴丁酰草胺、氯甲丹、环庚草醚、苯丙隆、乙苯酰草、膦铵素、威百亩、稗草畏、氯嗪草、棉隆、苯氧丙胺津和溴甲烷的其他除草剂。
7.根据权利要求5的方法,其中使式I的3-苯基尿嘧啶与草甘膦或其可农用盐组合使用。
8.根据权利要求7的方法,其中使式I的3-苯基尿嘧啶与草甘膦或其可农用盐和一种或多种其他除草剂B或其可农用盐组合使用。
9.根据权利要求5、6或8中任一项的方法,其中其他除草剂B选自灭草烟、咪草烟、咪草啶酸、甲基咪草烟、灭草喹、氯嘧黄隆、氟唑啶草、喹禾灵、精喹禾灵、吡氟禾草灵、精吡氟禾草灵、唑禾草灵、高唑禾草灵、枯杀达、稀禾定、烯草酮、噻草酮、醌肟草及其可农用盐和衍生物。
10.根据权利要求9的方法,其中其他除草剂B为咪草烟或咪草啶酸或其可农用盐。
11.根据前述权利要求中任一项的方法,其中使式I的3-苯基尿嘧啶与一种或多种安全剂C或其可农用盐组合使用。
12.根据前述权利要求中任一项的方法,其中在抗草甘膦杂草或作物出苗后施用任选与所述其他除草剂B组合和/或任选与所述安全剂C组合的3-苯基尿嘧啶。
13.根据权利要求12的方法,其中在抗草甘膦杂草或作物出苗后但在所需作物种植、播种或出苗前施用3-苯基尿嘧啶。
14.如权利要求1-3中任一项所定义的3-苯基尿嘧啶任选与一种或多种如权利要求5-10中任一项所定义的其他除草剂B组合和/或任选与一种或多种如权利要求11所定义的安全剂C组合在防治抗草甘膦杂草或作物中的用途。
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WO (1) | WO2007014758A1 (zh) |
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CN102651971A (zh) * | 2009-12-09 | 2012-08-29 | 巴斯夫欧洲公司 | 含有嘧啶肟草醚和草甘膦的液体悬浮浓缩物配制剂 |
CN102946714A (zh) * | 2009-09-01 | 2013-02-27 | 巴斯夫农业化学产品公司 | 耐受除草剂的植物 |
CN105454240A (zh) * | 2015-12-28 | 2016-04-06 | 南京华洲药业有限公司 | 一种含苯嘧磺草胺与炔草酯的混合除草剂 |
WO2019106568A1 (en) * | 2017-11-29 | 2019-06-06 | Basf Se | Plants having increased tolerance to herbicides |
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BRPI0620374B1 (pt) | 2005-12-23 | 2015-08-11 | Basf Se | Método de controle de erva daninha aquática hydrilla verticillata |
US9210930B2 (en) | 2005-12-23 | 2015-12-15 | Basf Se | Control of submerged aquatic vegetation |
BRPI0619639A2 (pt) | 2005-12-23 | 2012-12-11 | Basf Se | método para controlar ervas daninhas aquáticas, e, uso de uma composição |
AR075467A1 (es) * | 2008-10-22 | 2011-04-06 | Basf Se | Uso de inhibidores de protoporfirinogeno oxidasa en plantas cultivadas |
WO2011023759A2 (en) | 2009-08-27 | 2011-03-03 | Basf Se | Aqueous suspension concentrate formulations containing saflufenacil |
BR112012004051B1 (pt) | 2009-08-27 | 2021-02-17 | Basf Se | formulação de concentrado aquoso, uso da formulação de concentrado aquoso e metodo para controlar vegetação indesejada |
AU2010329961B2 (en) | 2009-12-09 | 2014-12-04 | Basf Se | Liquid suspension concentrate formulations containing saflufenacil |
UY33860A (es) * | 2011-01-07 | 2012-08-31 | Dow Agrosciences Llc | Tolerancia aumentada de plantas habilitadas por dht a herbicidas auxínicos resultante de diferencias de porciones en estructuras moleculares del herbicida |
PT2665361E (pt) * | 2011-01-18 | 2016-01-11 | Dow Agrosciences Llc | Composição herbicida sinérgica contendo penoxsulam, triclopir e imazetapir ou imazamox |
AU2013247523B2 (en) * | 2012-04-12 | 2015-12-03 | Dongbu Farm Hannong Co., Ltd. | Herbicidal composition comprising uracil compound as active ingredient |
JP2017019840A (ja) | 2016-07-29 | 2017-01-26 | 住友化学株式会社 | 農作物における有害生物の防除方法 |
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FR2734842B1 (fr) * | 1995-06-02 | 1998-02-27 | Rhone Poulenc Agrochimie | Sequence adn d'un gene de l'hydroxy-phenyl pyruvate dioxygenase et obtention de plantes contenant un gene de l'hydroxy-phenyl pyruvate dioxygenase, tolerantes a certains herbicides |
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DE19846792A1 (de) * | 1998-10-10 | 2000-04-13 | Hoechst Schering Agrevo Gmbh | Benzoylcyclohexandione, Verfahren zur ihrer Herstellung und ihre Verwendung als Herbizide und Pflanzenwachstumsregulatoren |
SI1226127T1 (sl) * | 2000-05-04 | 2009-10-31 | Basf Se | Substituirani fenilsulfamoil karboksamidi |
DK1429609T3 (da) * | 2001-09-14 | 2007-07-02 | Basf Ag | Herbicide blandinger baseret på 3 - uracil |
EA007949B1 (ru) * | 2003-03-13 | 2007-02-27 | Басф Акциенгезельшафт | Гербицидные смеси на основе 3-фенилурацилов |
-
2006
- 2006-07-31 PE PE2006000924A patent/PE20070534A1/es not_active Application Discontinuation
- 2006-07-31 AR ARP060103331A patent/AR056436A1/es not_active Application Discontinuation
- 2006-08-01 TW TW095128150A patent/TW200738138A/zh unknown
- 2006-08-01 WO PCT/EP2006/007614 patent/WO2007014758A1/en active Application Filing
- 2006-08-01 KR KR1020087002610A patent/KR20080058323A/ko not_active Application Discontinuation
- 2006-08-01 EA EA200800390A patent/EA200800390A1/ru unknown
- 2006-08-01 EP EP06762937A patent/EP1926374A1/en not_active Withdrawn
- 2006-08-01 CN CNA200680028370XA patent/CN101232813A/zh active Pending
- 2006-08-01 MX MX2008001097A patent/MX2008001097A/es unknown
- 2006-08-01 CA CA002617247A patent/CA2617247A1/en not_active Abandoned
- 2006-08-01 JP JP2008524425A patent/JP2009503004A/ja not_active Withdrawn
- 2006-08-01 US US11/997,165 patent/US20080227637A1/en not_active Abandoned
- 2006-08-01 AU AU2006275053A patent/AU2006275053A1/en not_active Abandoned
- 2006-08-01 BR BRPI0614194A patent/BRPI0614194A2/pt not_active IP Right Cessation
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
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CN102946714A (zh) * | 2009-09-01 | 2013-02-27 | 巴斯夫农业化学产品公司 | 耐受除草剂的植物 |
CN102946714B (zh) * | 2009-09-01 | 2017-10-10 | 巴斯夫农业化学产品公司 | 耐受除草剂的植物 |
CN102651971A (zh) * | 2009-12-09 | 2012-08-29 | 巴斯夫欧洲公司 | 含有嘧啶肟草醚和草甘膦的液体悬浮浓缩物配制剂 |
CN102651971B (zh) * | 2009-12-09 | 2015-05-13 | 巴斯夫欧洲公司 | 含有苯嘧磺草胺和草甘膦的液体悬浮浓缩物配制剂 |
CN105454240A (zh) * | 2015-12-28 | 2016-04-06 | 南京华洲药业有限公司 | 一种含苯嘧磺草胺与炔草酯的混合除草剂 |
WO2019106568A1 (en) * | 2017-11-29 | 2019-06-06 | Basf Se | Plants having increased tolerance to herbicides |
CN111801012A (zh) * | 2017-11-29 | 2020-10-20 | 巴斯夫欧洲公司 | 具有增加的除草剂耐受性的植物 |
US11479786B2 (en) | 2017-11-29 | 2022-10-25 | Basf Se | Plants having increased tolerance to herbicides |
Also Published As
Publication number | Publication date |
---|---|
WO2007014758A1 (en) | 2007-02-08 |
CA2617247A1 (en) | 2007-02-08 |
BRPI0614194A2 (pt) | 2016-11-22 |
AR056436A1 (es) | 2007-10-10 |
TW200738138A (en) | 2007-10-16 |
KR20080058323A (ko) | 2008-06-25 |
PE20070534A1 (es) | 2007-06-11 |
AU2006275053A1 (en) | 2007-02-08 |
EP1926374A1 (en) | 2008-06-04 |
US20080227637A1 (en) | 2008-09-18 |
WO2007014758A8 (en) | 2008-03-27 |
EA200800390A1 (ru) | 2008-08-29 |
JP2009503004A (ja) | 2009-01-29 |
MX2008001097A (es) | 2008-03-11 |
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