JP5647238B2 - グリホサート塩及びジカンバ塩を含有する除草剤濃縮組成物 - Google Patents
グリホサート塩及びジカンバ塩を含有する除草剤濃縮組成物 Download PDFInfo
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- JP5647238B2 JP5647238B2 JP2012517713A JP2012517713A JP5647238B2 JP 5647238 B2 JP5647238 B2 JP 5647238B2 JP 2012517713 A JP2012517713 A JP 2012517713A JP 2012517713 A JP2012517713 A JP 2012517713A JP 5647238 B2 JP5647238 B2 JP 5647238B2
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- salt
- potassium
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- dicamba
- glyphosate
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- 239000000203 mixture Substances 0.000 title claims description 87
- IWEDIXLBFLAXBO-UHFFFAOYSA-N dicamba Chemical class COC1=C(Cl)C=CC(Cl)=C1C(O)=O IWEDIXLBFLAXBO-UHFFFAOYSA-N 0.000 title claims description 41
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical class OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 title claims description 40
- 230000002363 herbicidal effect Effects 0.000 title claims description 32
- 239000004009 herbicide Substances 0.000 title claims description 14
- 239000012141 concentrate Substances 0.000 title claims description 8
- -1 amine salt Chemical class 0.000 claims description 35
- 239000005562 Glyphosate Substances 0.000 claims description 27
- 229940097068 glyphosate Drugs 0.000 claims description 27
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical group [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 26
- 239000011591 potassium Substances 0.000 claims description 26
- 229910052700 potassium Inorganic materials 0.000 claims description 26
- 239000005504 Dicamba Substances 0.000 claims description 25
- 239000004094 surface-active agent Substances 0.000 claims description 19
- 150000003839 salts Chemical class 0.000 claims description 13
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 239000002253 acid Substances 0.000 claims description 10
- 150000003973 alkyl amines Chemical group 0.000 claims description 10
- 239000004480 active ingredient Substances 0.000 claims description 9
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 239000006184 cosolvent Substances 0.000 claims description 9
- 238000011068 loading method Methods 0.000 claims description 9
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 claims description 8
- 229920006395 saturated elastomer Polymers 0.000 claims description 8
- 239000005631 2,4-Dichlorophenoxyacetic acid Substances 0.000 claims description 7
- YIVXMZJTEQBPQO-UHFFFAOYSA-N 2,4-DB Chemical compound OC(=O)CCCOC1=CC=C(Cl)C=C1Cl YIVXMZJTEQBPQO-UHFFFAOYSA-N 0.000 claims description 6
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 claims description 6
- LLWADFLAOKUBDR-UHFFFAOYSA-N 2-methyl-4-chlorophenoxybutyric acid Chemical compound CC1=CC(Cl)=CC=C1OCCCC(O)=O LLWADFLAOKUBDR-UHFFFAOYSA-N 0.000 claims description 5
- 239000005575 MCPB Substances 0.000 claims description 5
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 4
- UEEJHVSXFDXPFK-UHFFFAOYSA-N N-dimethylaminoethanol Chemical compound CN(C)CCO UEEJHVSXFDXPFK-UHFFFAOYSA-N 0.000 claims description 4
- WHKUVVPPKQRRBV-UHFFFAOYSA-N Trasan Chemical compound CC1=CC(Cl)=CC=C1OCC(O)=O WHKUVVPPKQRRBV-UHFFFAOYSA-N 0.000 claims description 4
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical compound C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 claims description 4
- 229960002887 deanol Drugs 0.000 claims description 4
- 239000012972 dimethylethanolamine Substances 0.000 claims description 4
- 238000000034 method Methods 0.000 claims description 4
- 239000002794 2,4-DB Substances 0.000 claims description 3
- HXKWSTRRCHTUEC-UHFFFAOYSA-N 2,4-Dichlorophenoxyaceticacid Chemical compound OC(=O)C(Cl)OC1=CC=C(Cl)C=C1 HXKWSTRRCHTUEC-UHFFFAOYSA-N 0.000 claims description 3
- 239000005500 Clopyralid Substances 0.000 claims description 3
- 239000005558 Fluroxypyr Substances 0.000 claims description 3
- 239000005574 MCPA Substances 0.000 claims description 3
- 101150039283 MCPB gene Proteins 0.000 claims description 3
- 239000005627 Triclopyr Substances 0.000 claims description 3
- 125000004183 alkoxy alkyl group Chemical group 0.000 claims description 3
- 229960001231 choline Drugs 0.000 claims description 3
- HUBANNPOLNYSAD-UHFFFAOYSA-N clopyralid Chemical compound OC(=O)C1=NC(Cl)=CC=C1Cl HUBANNPOLNYSAD-UHFFFAOYSA-N 0.000 claims description 3
- MEFQWPUMEMWTJP-UHFFFAOYSA-N fluroxypyr Chemical compound NC1=C(Cl)C(F)=NC(OCC(O)=O)=C1Cl MEFQWPUMEMWTJP-UHFFFAOYSA-N 0.000 claims description 3
- SIOXPEMLGUPBBT-UHFFFAOYSA-N picolinic acid Chemical compound OC(=O)C1=CC=CC=N1 SIOXPEMLGUPBBT-UHFFFAOYSA-N 0.000 claims description 3
- LIOPHZNMBKHGAV-UHFFFAOYSA-M potassium;2-(phosphonomethylamino)acetate Chemical compound [K+].OC(=O)CNCP(O)([O-])=O LIOPHZNMBKHGAV-UHFFFAOYSA-M 0.000 claims description 3
- LOAUVZALPPNFOQ-UHFFFAOYSA-N quinaldic acid Chemical compound C1=CC=CC2=NC(C(=O)O)=CC=C21 LOAUVZALPPNFOQ-UHFFFAOYSA-N 0.000 claims description 3
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 claims description 3
- 230000002708 enhancing effect Effects 0.000 claims description 2
- FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 claims 2
- 239000005468 Aminopyralid Substances 0.000 claims 1
- 239000004381 Choline salt Substances 0.000 claims 1
- NIXXQNOQHKNPEJ-UHFFFAOYSA-N aminopyralid Chemical compound NC1=CC(Cl)=NC(C(O)=O)=C1Cl NIXXQNOQHKNPEJ-UHFFFAOYSA-N 0.000 claims 1
- 235000019417 choline salt Nutrition 0.000 claims 1
- RVJMEWSAFHIEJX-UHFFFAOYSA-M dicamba-potassium Chemical compound [K+].COC1=C(Cl)C=CC(Cl)=C1C([O-])=O RVJMEWSAFHIEJX-UHFFFAOYSA-M 0.000 claims 1
- 150000003248 quinolines Chemical class 0.000 claims 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 11
- 238000009472 formulation Methods 0.000 description 11
- 239000000243 solution Substances 0.000 description 8
- 150000001412 amines Chemical class 0.000 description 7
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 6
- 239000003795 chemical substances by application Substances 0.000 description 6
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 239000012266 salt solution Substances 0.000 description 6
- 238000003860 storage Methods 0.000 description 5
- 229930192334 Auxin Natural products 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- 239000002363 auxin Substances 0.000 description 4
- 235000019441 ethanol Nutrition 0.000 description 4
- SEOVTRFCIGRIMH-UHFFFAOYSA-N indole-3-acetic acid Chemical compound C1=CC=C2C(CC(=O)O)=CNC2=C1 SEOVTRFCIGRIMH-UHFFFAOYSA-N 0.000 description 4
- 238000005191 phase separation Methods 0.000 description 4
- 238000002360 preparation method Methods 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical class CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 3
- 238000001556 precipitation Methods 0.000 description 3
- IAJOBQBIJHVGMQ-UHFFFAOYSA-N 2-amino-4-[hydroxy(methyl)phosphoryl]butanoic acid Chemical compound CP(O)(=O)CCC(N)C(O)=O IAJOBQBIJHVGMQ-UHFFFAOYSA-N 0.000 description 2
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 2
- 239000005561 Glufosinate Substances 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000005595 Picloram Substances 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 2
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 2
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 2
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-UHFFFAOYSA-N 2,4-D Chemical compound OC(=O)COC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-UHFFFAOYSA-N 0.000 description 1
- QURLONWWPWCPIC-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol;3,6-dichloro-2-methoxybenzoic acid Chemical compound NCCOCCO.COC1=C(Cl)C=CC(Cl)=C1C(O)=O QURLONWWPWCPIC-UHFFFAOYSA-N 0.000 description 1
- SBASXUCJHJRPEV-UHFFFAOYSA-N 2-(2-methoxyethoxy)ethanol Chemical compound COCCOCCO SBASXUCJHJRPEV-UHFFFAOYSA-N 0.000 description 1
- CAAMSDWKXXPUJR-UHFFFAOYSA-N 3,5-dihydro-4H-imidazol-4-one Chemical class O=C1CNC=N1 CAAMSDWKXXPUJR-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003242 anti bacterial agent Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 229910052799 carbon Inorganic materials 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000000470 constituent Substances 0.000 description 1
- 238000005260 corrosion Methods 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 238000002425 crystallisation Methods 0.000 description 1
- 230000008025 crystallization Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- XXUJMEYKYHETBZ-UHFFFAOYSA-N ethyl 4-nitrophenyl ethylphosphonate Chemical compound CCOP(=O)(CC)OC1=CC=C([N+]([O-])=O)C=C1 XXUJMEYKYHETBZ-UHFFFAOYSA-N 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- ZEKANFGSDXODPD-UHFFFAOYSA-N glyphosate-isopropylammonium Chemical compound CC(C)N.OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-N 0.000 description 1
- 239000012456 homogeneous solution Substances 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- HNXNKTMIVROLTK-UHFFFAOYSA-N n,n-dimethyldecanamide Chemical compound CCCCCCCCCC(=O)N(C)C HNXNKTMIVROLTK-UHFFFAOYSA-N 0.000 description 1
- VHRUBWHAOUIMDW-UHFFFAOYSA-N n,n-dimethyloctanamide Chemical compound CCCCCCCC(=O)N(C)C VHRUBWHAOUIMDW-UHFFFAOYSA-N 0.000 description 1
- VDCHTAFVUAPYGO-UHFFFAOYSA-N n-methylmethanamine;2-(phosphonomethylamino)acetic acid Chemical compound CNC.OC(=O)CNCP(O)(O)=O VDCHTAFVUAPYGO-UHFFFAOYSA-N 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 239000005022 packaging material Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 230000008635 plant growth Effects 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 238000003971 tillage Methods 0.000 description 1
- 239000000080 wetting agent Substances 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
- A01N57/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds
- A01N57/18—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds
- A01N57/20—Biocides, pest repellants or attractants, or plant growth regulators containing organic phosphorus compounds having phosphorus-to-carbon bonds containing acyclic or cycloaliphatic radicals
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/10—Aromatic or araliphatic carboxylic acids, or thio analogues thereof; Derivatives thereof
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/36—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
- A01N37/38—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system
- A01N37/40—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 at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids having at least one oxygen or sulfur atom attached to an aromatic ring system having at least one carboxylic group or a thio analogue, or a derivative thereof, and one oxygen or sulfur atom attached to the same aromatic ring system
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Toxicology (AREA)
Description
(a)水、
(b)グリホサートのカリウム若しくはアミン塩、及び
(c)ジカンバのカリウム若しくはアミン塩を含み、
ここで、(i)該グリホサートの塩は、カリウム又は2級、3級若しくは4級アルキルアミン又は1級、2級、3級若しくは4級のアルカノールアミン、アルキルアルカノールアミン若しくはアルコキシアルカノールアミン塩であり、該アルキル及びアルカノール基は飽和しておりそれぞれC1−C4炭素原子を含有し、(ii)該ジカンバの塩は、カリウム又は2級、3級若しくは4級アルキルアミン又は1級、2級、3級若しくは4級のアルカノールアミン、アルキルアルカノールアミン若しくはアルコキシアルカノールアミン塩であり、該アルキル及びアルカノール基は飽和しておりそれぞれC1−C4炭素原子を含有し、(iii)該組成物は、該グリホサート塩及び該ジカンバ塩の少なくとも300gae/Lの全有効成分装填量を含有し、(iv)1リットル当たりのグラム酸当量(gae/L)で表示した該グリホサート塩(gae/L)対該ジカンバ塩(gae/L)の酸当量比は、1:1〜3:1であり、及び(v)pHは6.0〜8.0である高強度の水性除草剤濃縮組成物を提供する。さらに、1つ又はそれ以上の共溶媒及び/又は有効性増強界面活性剤を、高装填量を維持する限りは場合により該高強度組成物中に組み込むことができる。場合により、第2のオーキシン型除草剤を本組成物中に組み込むことができる。オーキシン型除草剤には、クロロフェノキシ酸、例えば2,4−ジクロロフェノキシ酢酸[2,4−D]、2,4−ジクロロフェノキシ酪酸[2,4−DB]、(4−クロロ−2−メチルフェノキシ)酢酸[MCPA]及び4−(4−クロロ−2−メチルフェノキシ)ブタン酸[MCPB];ピリジンカルボン酸、例えばピクロラム、アミノピラリド、フルロキシピル、クロピラリド及びトリクロピル;並びにキノリンカルボン酸、例えばキンメラック及びキンクロラックが含まれる。
(a)水、
(b)グリホサートのカリウム若しくはアミン塩、
(c)ジカンバのカリウム若しくはアミン塩を含み、
ここで、(i)該グリホサートの塩は、カリウム又は2級、3級若しくは4級アルキルアミン又は1級、2級、3級若しくは4級のアルカノールアミン、アルキルアルカノールアミン若しくはアルコキシアルカノールアミン塩であり、該アルキル及びアルカノール基は飽和しておりそれぞれC1−C4炭素原子を含有し、(ii)該ジカンバの塩は、カリウム又は2級、3級若しくは4級アルキルアミン又は1級、2級、3級若しくは4級のアルカノールアミン、アルキルアルカノールアミン若しくはアルコキシアルカノールアミン塩であり、該アルキル及びアルカノール基は飽和しておりそれぞれC1−C4炭素原子を含有し、(iii)該組成物は、該グリホサートのアミン塩又はカリウム塩及び該該ジカンバ塩又はカリウム塩の少なくとも300gae/Lの全有効成分装填量を含有し、(iv)該グリホサート塩対該ジカンバ塩の酸当量比は、1:1〜3:1であり、及び(v)pHは6.0〜8.0である高強度の水性除草剤濃縮組成物を提供する。
組成物は、表1に記載のグリホサート塩溶液を表2に記載のジカンバ塩溶液及び必要であれば水と混合することによって調製した。表3に例示した実施例は、グリホサート及びジカンバのIPA塩を含有する先行技術組成物の貯蔵安定性を示している。表4に提示した実施例は、本発明を実証している。
組成物(表4に記載の製剤ID 10を備える)は、4.35gのグリホサートジメチルアミン塩溶液(表1のG−1−1)と1.37gのジカンバジグリコールアミン塩溶液(表2のD−1−2、共溶媒として25重量%のジエチレングリコールを含有する)とを3:1の重量比で混合することによって調製した。全活性含量は、480g ae/Lである。最終組成物は、6重量%のジエチレングリコールを含有する。最終組成物は、周囲温度での調製後に透明で均質な溶液を形成した。最終組成物は、54℃、0℃、−10℃、及び−20℃で15日間にわたって、相分離又は結晶形成を伴わずに安定生かつ均質のままであった。本組成物は、透明で均質な自由流動液体であった。
Claims (10)
- (a)水、
(b)グリホサートのカリウム若しくはアミン塩、及び
(c)ジカンバのカリウム若しくはアミン塩
を含む、水性除草剤濃縮組成物であって、
ここで、(i)前記グリホサートの塩は、カリウム又は2級、3級若しくは4級アルキルアミン又は1級、2級、3級若しくは4級のアルカノールアミン、アルキルアルカノールアミン若しくはアルコキシアルカノールアミン塩であり、前記アルキル及びアルカノール基は飽和しておりそれぞれC1−C4炭素原子を含有し、(ii)前記ジカンバの塩は、カリウム又は2級、3級若しくは4級アルキルアミン又は1級、2級、3級若しくは4級のアルカノールアミン、アルキルアルカノールアミン若しくはアルコキシアルカノールアミン塩であり、前記アルキル及びアルカノール基は飽和しておりそれぞれC1−C4炭素原子を含有し、(iii)前記組成物は、前記グリホサートのカリウム又はアミン塩及び前記ジカンバのカリウム又はアミン塩の少なくとも300gae/Lの全有効成分装填量を含有し、(iv)前記グリホサートのカリウム又はアミン塩対前記ジカンバのカリウム又はアミン塩の酸当量比は、1:1〜3:1であり、及び(v)pHは6.0〜8.0である、組成物。 - 前記グリホサートのカリウム又はアミン塩及び前記ジカンバのカリウム又はアミン塩の450g(グラム)より高い酸当量の全有効成分装填量を含有する、請求項1に記載の組成物。
- 前記グリホサートのカリウム又はアミン塩対前記ジカンバのカリウム又はアミン塩の前記酸当量比は、1.5:1〜3:1である、請求項1に記載の組成物。
- 前記pHは、6.5〜7.5である、請求項1に記載の組成物。
- 前記グリホサート塩は、カリウム若しくはモノエタノールアミン、ジメチルエタノールアミン、ジメチルアミン、ジグリコールアミン又はコリン塩である、請求項1に記載の組成物。
- 前記ジカンバ塩は、カリウム又はジメチルアミン、モノエタノールアミン、ジメチルエタノールアミン、コリン若しくはジグリコールアミン塩である、請求項1に記載の組成物。
- 少なくとも1つの共溶媒を20g/L〜200g/Lの量で含む、請求項1に記載の組成物。
- 少なくとも1つの有効性増強界面活性剤を20g/L〜200g/Lの量で含む、請求項1に記載の組成物。
- 2,4−ジクロロフェノキシ酢酸[2,4−D]、2,4−ジクロロフェノキシ酪酸[2,4−DB]、(4−クロロ−2−メチルフェノキシ)酢酸[MCPA]及び4−(4−クロロ−2−メチルフェノキシ)ブタン酸[MCPB]からなる群から選択されるクロロフェノキシ酸;ピクロラム、アミノピラリド、フルロキシピル、クロピラリド及びトリクロピルからなる群から選択されるピリジンカルボン酸;又はキンメラック及びキンクロラックからなる群から選択されるキノリンカルボン酸を含む第2オーキシン型除草剤を含む、請求項1に記載の組成物。
- グリホサート及びジカンバの両方に対して抵抗性又は耐性である農作物における望ましくない植物を制御する方法であって、前記望ましくない植物及びグリホサート及びジカンバの両方に抵抗性又は耐性である前記農作物に請求項1から9のいずれか一項に記載の水で希釈した組成物を適用する工程を含む方法。
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JP2013542172A (ja) * | 2010-05-04 | 2013-11-21 | ダウ アグロサイエンシィズ エルエルシー | ジカンバ誘導体およびグリホセート誘導体を含有する相乗的除草剤組成物 |
JP2016006073A (ja) * | 2010-05-04 | 2016-01-14 | ダウ アグロサイエンシィズ エルエルシー | ジカンバ誘導体およびグリホセート誘導体を含有する相乗的除草剤組成物 |
JP2018058839A (ja) * | 2010-05-04 | 2018-04-12 | ダウ アグロサイエンシィズ エルエルシー | ジカンバ誘導体およびグリホセート誘導体を含有する相乗的除草剤組成物 |
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JP2012531425A (ja) | 2012-12-10 |
PL2445337T3 (pl) | 2018-09-28 |
MX2011014022A (es) | 2012-09-07 |
CA2765888A1 (en) | 2010-12-29 |
BRPI1012682B1 (pt) | 2018-04-17 |
EP2445337A2 (en) | 2012-05-02 |
IL217168A0 (en) | 2012-02-29 |
NZ597054A (en) | 2012-12-21 |
CA2765888C (en) | 2017-11-21 |
IL217168A (en) | 2015-05-31 |
BRPI1012682B8 (pt) | 2022-10-11 |
CN102480936A (zh) | 2012-05-30 |
BRPI1012682A2 (pt) | 2015-09-15 |
AU2010264433A1 (en) | 2012-01-19 |
EP2445337B1 (en) | 2018-04-18 |
WO2010151622A3 (en) | 2011-05-26 |
WO2010151622A2 (en) | 2010-12-29 |
AU2010264433B2 (en) | 2014-03-27 |
ES2670370T3 (es) | 2018-05-30 |
ZA201109374B (en) | 2013-02-27 |
US9288984B2 (en) | 2016-03-22 |
PT2445337T (pt) | 2018-07-25 |
CN102480936B (zh) | 2015-03-25 |
US20100331182A1 (en) | 2010-12-30 |
PE20121080A1 (es) | 2012-08-10 |
AR077246A1 (es) | 2011-08-10 |
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