JP2012524812A - フィールド・レディ・スプレーおよびタンク混合物中における窒素含有イセチオン酸塩 - Google Patents
フィールド・レディ・スプレーおよびタンク混合物中における窒素含有イセチオン酸塩 Download PDFInfo
- Publication number
- JP2012524812A JP2012524812A JP2012507403A JP2012507403A JP2012524812A JP 2012524812 A JP2012524812 A JP 2012524812A JP 2012507403 A JP2012507403 A JP 2012507403A JP 2012507403 A JP2012507403 A JP 2012507403A JP 2012524812 A JP2012524812 A JP 2012524812A
- Authority
- JP
- Japan
- Prior art keywords
- nitrogen
- composition
- agricultural
- isethionate
- active ingredient
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 61
- SUMDYPCJJOFFON-UHFFFAOYSA-N isethionic acid Chemical compound OCCS(O)(=O)=O SUMDYPCJJOFFON-UHFFFAOYSA-N 0.000 title claims abstract description 48
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 title claims abstract description 25
- 239000007921 spray Substances 0.000 title claims abstract description 22
- 239000004094 surface-active agent Substances 0.000 claims abstract description 27
- 239000004480 active ingredient Substances 0.000 claims abstract description 20
- -1 cyclic amine Chemical class 0.000 claims description 30
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims description 21
- 229940045996 isethionic acid Drugs 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- 239000003128 rodenticide Substances 0.000 claims description 9
- 230000002378 acidificating effect Effects 0.000 claims description 8
- 238000000034 method Methods 0.000 claims description 8
- 239000002917 insecticide Substances 0.000 claims description 7
- 239000003760 tallow Substances 0.000 claims description 7
- 150000003973 alkyl amines Chemical class 0.000 claims description 6
- 239000000758 substrate Substances 0.000 claims description 6
- 230000000895 acaricidal effect Effects 0.000 claims description 4
- 239000000642 acaricide Substances 0.000 claims description 4
- 125000002091 cationic group Chemical group 0.000 claims description 4
- 239000003750 molluscacide Substances 0.000 claims description 4
- 230000002013 molluscicidal effect Effects 0.000 claims description 4
- 239000005648 plant growth regulator Substances 0.000 claims description 4
- 239000002689 soil Substances 0.000 claims description 4
- LLOHIFXFHGMBNO-UHFFFAOYSA-N azane;2-hydroxyethanesulfonic acid Chemical class [NH4+].OCCS([O-])(=O)=O LLOHIFXFHGMBNO-UHFFFAOYSA-N 0.000 claims description 3
- 239000003139 biocide Substances 0.000 claims description 3
- 239000005645 nematicide Substances 0.000 claims description 3
- 239000003619 algicide Substances 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000011814 protection agent Substances 0.000 claims description 2
- 239000005562 Glyphosate Substances 0.000 description 17
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 17
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 17
- 235000011130 ammonium sulphate Nutrition 0.000 description 17
- 229940097068 glyphosate Drugs 0.000 description 17
- 239000003337 fertilizer Substances 0.000 description 14
- 150000003839 salts Chemical class 0.000 description 14
- 239000004009 herbicide Substances 0.000 description 13
- 150000001412 amines Chemical class 0.000 description 8
- 239000000575 pesticide Substances 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 239000000243 solution Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000011575 calcium Substances 0.000 description 4
- 239000008233 hard water Substances 0.000 description 4
- 230000002363 herbicidal effect Effects 0.000 description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 239000000126 substance Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ROSDSFDQCJNGOL-UHFFFAOYSA-N Dimethylamine Chemical compound CNC ROSDSFDQCJNGOL-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- JLVVSXFLKOJNIY-UHFFFAOYSA-N Magnesium ion Chemical compound [Mg+2] JLVVSXFLKOJNIY-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 125000002877 alkyl aryl group Chemical group 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 229910052791 calcium Inorganic materials 0.000 description 2
- 229910001424 calcium ion Inorganic materials 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 229940031098 ethanolamine Drugs 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- ZEKANFGSDXODPD-UHFFFAOYSA-N glyphosate-isopropylammonium Chemical compound CC(C)N.OC(=O)CNCP(O)(O)=O ZEKANFGSDXODPD-UHFFFAOYSA-N 0.000 description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 description 2
- 150000002500 ions Chemical class 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- JJWLVOIRVHMVIS-UHFFFAOYSA-N isopropylamine Chemical compound CC(C)N JJWLVOIRVHMVIS-UHFFFAOYSA-N 0.000 description 2
- 239000011777 magnesium Substances 0.000 description 2
- 229910052749 magnesium Inorganic materials 0.000 description 2
- 229910001425 magnesium ion Inorganic materials 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 239000011707 mineral Substances 0.000 description 2
- 235000010755 mineral Nutrition 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 229910052698 phosphorus Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- FGIUAXJPYTZDNR-UHFFFAOYSA-N potassium nitrate Chemical compound [K+].[O-][N+]([O-])=O FGIUAXJPYTZDNR-UHFFFAOYSA-N 0.000 description 2
- WGYKZJWCGVVSQN-UHFFFAOYSA-N propylamine Chemical class CCCN WGYKZJWCGVVSQN-UHFFFAOYSA-N 0.000 description 2
- 238000003908 quality control method Methods 0.000 description 2
- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- VWDWKYIASSYTQR-UHFFFAOYSA-N sodium nitrate Chemical compound [Na+].[O-][N+]([O-])=O VWDWKYIASSYTQR-UHFFFAOYSA-N 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 241000894007 species Species 0.000 description 2
- NRZWQKGABZFFKE-UHFFFAOYSA-N trimethylsulfonium Chemical class C[S+](C)C NRZWQKGABZFFKE-UHFFFAOYSA-N 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- RASUWBZHFDVNCQ-VKHMYHEASA-N (2s)-2-(phosphonomethylamino)propanoic acid Chemical compound OC(=O)[C@H](C)NCP(O)(O)=O RASUWBZHFDVNCQ-VKHMYHEASA-N 0.000 description 1
- WTFAGPBUAGFMQX-UHFFFAOYSA-N 1-[2-[2-(2-aminopropoxy)propoxy]propoxy]propan-2-amine Chemical compound CC(N)COCC(C)OCC(C)OCC(C)N WTFAGPBUAGFMQX-UHFFFAOYSA-N 0.000 description 1
- OVSKIKFHRZPJSS-DOMIDYPGSA-N 2-(2,4-dichlorophenoxy)acetic acid Chemical compound OC(=O)[14CH2]OC1=CC=C(Cl)C=C1Cl OVSKIKFHRZPJSS-DOMIDYPGSA-N 0.000 description 1
- IEORSVTYLWZQJQ-UHFFFAOYSA-N 2-(2-nonylphenoxy)ethanol Chemical group CCCCCCCCCC1=CC=CC=C1OCCO IEORSVTYLWZQJQ-UHFFFAOYSA-N 0.000 description 1
- PAWQVTBBRAZDMG-UHFFFAOYSA-N 2-(3-bromo-2-fluorophenyl)acetic acid Chemical compound OC(=O)CC1=CC=CC(Br)=C1F PAWQVTBBRAZDMG-UHFFFAOYSA-N 0.000 description 1
- 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 1
- WBIQQQGBSDOWNP-UHFFFAOYSA-N 2-dodecylbenzenesulfonic acid Chemical class CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O WBIQQQGBSDOWNP-UHFFFAOYSA-N 0.000 description 1
- 241000224489 Amoeba Species 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 235000002568 Capsicum frutescens Nutrition 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- PIICEJLVQHRZGT-UHFFFAOYSA-N Ethylenediamine Chemical compound NCCN PIICEJLVQHRZGT-UHFFFAOYSA-N 0.000 description 1
- 239000005561 Glufosinate Substances 0.000 description 1
- FYYHWMGAXLPEAU-UHFFFAOYSA-N Magnesium Chemical compound [Mg] FYYHWMGAXLPEAU-UHFFFAOYSA-N 0.000 description 1
- YNDPLKXRTGZNSG-UHFFFAOYSA-N N1CCOCC1.[P] Chemical compound N1CCOCC1.[P] YNDPLKXRTGZNSG-UHFFFAOYSA-N 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- 241000341511 Nematodes Species 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 239000005595 Picloram Substances 0.000 description 1
- ULUAUXLGCMPNKK-UHFFFAOYSA-N Sulfobutanedioic acid Chemical class OC(=O)CC(C(O)=O)S(O)(=O)=O ULUAUXLGCMPNKK-UHFFFAOYSA-N 0.000 description 1
- 239000005627 Triclopyr Substances 0.000 description 1
- DZHMRSPXDUUJER-UHFFFAOYSA-N [amino(hydroxy)methylidene]azanium;dihydrogen phosphate Chemical compound NC(N)=O.OP(O)(O)=O DZHMRSPXDUUJER-UHFFFAOYSA-N 0.000 description 1
- 125000001931 aliphatic group Chemical group 0.000 description 1
- HAMNKKUPIHEESI-UHFFFAOYSA-N aminoguanidine Chemical class NNC(N)=N HAMNKKUPIHEESI-UHFFFAOYSA-N 0.000 description 1
- LFVGISIMTYGQHF-UHFFFAOYSA-N ammonium dihydrogen phosphate Chemical compound [NH4+].OP(O)([O-])=O LFVGISIMTYGQHF-UHFFFAOYSA-N 0.000 description 1
- 229910000387 ammonium dihydrogen phosphate Inorganic materials 0.000 description 1
- 229940124323 amoebicide Drugs 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 230000000507 anthelmentic effect Effects 0.000 description 1
- 239000000059 antiamebic agent Substances 0.000 description 1
- 239000002518 antifoaming agent Substances 0.000 description 1
- 239000004599 antimicrobial Substances 0.000 description 1
- INQZXVMNJLSCGI-UHFFFAOYSA-M azanium;potassium;hydrogen phosphate Chemical compound [NH4+].[K+].OP([O-])([O-])=O INQZXVMNJLSCGI-UHFFFAOYSA-M 0.000 description 1
- 230000000975 bioactive effect Effects 0.000 description 1
- 230000003115 biocidal effect Effects 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 229920001400 block copolymer Polymers 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000013626 chemical specie Substances 0.000 description 1
- 150000003841 chloride salts Chemical class 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- JKWMSGQKBLHBQQ-UHFFFAOYSA-N diboron trioxide Chemical compound O=BOB=O JKWMSGQKBLHBQQ-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
- 210000000744 eyelid Anatomy 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000002401 inhibitory effect Effects 0.000 description 1
- 239000000077 insect repellent Substances 0.000 description 1
- 244000144972 livestock Species 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- MEFBJEMVZONFCJ-UHFFFAOYSA-N molybdate Chemical compound [O-][Mo]([O-])(=O)=O MEFBJEMVZONFCJ-UHFFFAOYSA-N 0.000 description 1
- 235000019837 monoammonium phosphate Nutrition 0.000 description 1
- 239000006012 monoammonium phosphate Substances 0.000 description 1
- 229910000402 monopotassium phosphate Inorganic materials 0.000 description 1
- 235000019796 monopotassium phosphate Nutrition 0.000 description 1
- RWYGQIQKHRMKFH-UHFFFAOYSA-N naphthalene;sulfuric acid Chemical class OS(O)(=O)=O.C1=CC=CC2=CC=CC=C21 RWYGQIQKHRMKFH-UHFFFAOYSA-N 0.000 description 1
- 238000006386 neutralization reaction Methods 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- PXHVJJICTQNCMI-UHFFFAOYSA-N nickel Substances [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 239000000618 nitrogen fertilizer Substances 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- FIKAKWIAUPDISJ-UHFFFAOYSA-L paraquat dichloride Chemical compound [Cl-].[Cl-].C1=C[N+](C)=CC=C1C1=CC=[N+](C)C=C1 FIKAKWIAUPDISJ-UHFFFAOYSA-L 0.000 description 1
- 239000003090 pesticide formulation Substances 0.000 description 1
- 125000000951 phenoxy group Chemical class [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 1
- NQQVFXUMIDALNH-UHFFFAOYSA-N picloram Chemical compound NC1=C(Cl)C(Cl)=NC(C(O)=O)=C1Cl NQQVFXUMIDALNH-UHFFFAOYSA-N 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 229920002503 polyoxyethylene-polyoxypropylene Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 239000001103 potassium chloride Substances 0.000 description 1
- 235000011164 potassium chloride Nutrition 0.000 description 1
- GNSKLFRGEWLPPA-UHFFFAOYSA-M potassium dihydrogen phosphate Chemical compound [K+].OP(O)([O-])=O GNSKLFRGEWLPPA-UHFFFAOYSA-M 0.000 description 1
- 239000004323 potassium nitrate Substances 0.000 description 1
- 235000010333 potassium nitrate Nutrition 0.000 description 1
- LWIHDJKSTIGBAC-UHFFFAOYSA-K potassium phosphate Substances [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 1
- OTYBMLCTZGSZBG-UHFFFAOYSA-L potassium sulfate Chemical compound [K+].[K+].[O-]S([O-])(=O)=O OTYBMLCTZGSZBG-UHFFFAOYSA-L 0.000 description 1
- 229910052939 potassium sulfate Inorganic materials 0.000 description 1
- 235000011151 potassium sulphates Nutrition 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 230000005180 public health Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 239000004317 sodium nitrate Substances 0.000 description 1
- 235000010344 sodium nitrate Nutrition 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000000153 supplemental effect Effects 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 239000004711 α-olefin 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
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)
- Cultivation Of Plants (AREA)
- Catching Or Destruction (AREA)
Abstract
Description
、修正または設計を行い本発明と同じ目的を実施するための他の組成物を得る基礎として容易に利用できることを当業界の専門家は理解すべきである。またこのような同等な組成物は、添付特許請求の範囲に記載された本発明の精神および範囲を逸脱するものではないことも当業界の専門家は理解すべきである。
酸塩(その中和しない酸が上記の特徴をもつもの)である。当業界の専門家は、上記の説明により本発明に使用される適切な窒素含有イセチオン酸を認知できるであろう。
殺アメーバ剤、殺原生動物剤、作物保護剤、およびこれらの組み合わせを含んでいることができる。このような農業用成分の例はPesticide Dictionary(the Farm Chemicals Handbookの中に含まれている)、またはthe British Crop Protection Society発行のPesticides Manualから検索することができる。これらの文献の内容は引用により本明細書に包含される。農業用活性成分はさらに国際公開WO 2010/009820号明細書に「生物活性物質」として記載された化学物質を含んでいることができる。この特許は引用により本明細書に包含される。国際公開WO 2010/009820号明細書には何の制約もなく本発明の具体化例に使用できる種々の農薬、殺黴剤、除草剤、殺虫剤、植物成長調節剤、殺鼠剤、殺ダニ剤, 殺軟体動物剤, 殺線虫剤および抗微生物剤に関する説明およびリストが含まれている。当業界の専門家は本発明に使用するための適当な農業用活性成分およびそれらの組み合わせを認知することができよう。
Claims (14)
- (a)少なくとも1種の窒素含有イセチオン酸塩、
(b)少なくとも1種の農業用活性成分、および
(c)少なくとも1種の表面活性剤を含んで成る農業用組成物であって、
該農業用組成物は、フィールド・レディ・スプレーまたはタンク混合物であることを特徴とする農業用組成物。 - 該少なくとも1種の窒素含有イセチオン酸塩は陽イオン性の窒素含有基を有し、該基はアルキルアミン、アルキルアルカノールアミン、または環式アミンであることを特徴とする請求項1記載の組成物。
- 該少なくとも1種の窒素含有イセチオン酸塩はアンモニウムイセチオン酸塩を含んで成ることを特徴とする請求項1記載の組成物。
- 該少なくとも1種の窒素含有イセチオン酸塩はタロウアミンイセチオン酸塩を含んで成ることを特徴とする請求項1記載の組成物。
- 該少なくとも1種の窒素含有イセチオン酸塩は窒素含有イセチオン酸塩の誘導体を含んで成ることを特徴とする請求項1記載の組成物。
- 該窒素含有イセチオン酸塩の誘導体は窒素含有メチルイセチオン酸塩を含んで成ることを特徴とする請求項5記載の組成物。
- 該少なくとも1種の窒素含有イセチオン酸塩はさらにイセチオン酸を含んで成ることを特徴とする請求項1記載の組成物。
- 該農業用活性成分は弱酸性の農業用活性成分を含んで成ることを特徴とする請求項1記載の組成物。
- 該農業用活性成分はn−フォスフォノメチルグリシンを含んで成ることを特徴とする請求項1記載の組成物。
- 該農業用活性成分は殺虫剤、殺黴剤、殺生物剤、殺軟体動物剤、殺藻剤、植物成長調節剤、駆虫剤、殺鼠剤、殺線虫剤、殺ダニ剤、殺アメーバ剤、殺原生動物剤、作物保護剤、およびこれらの組み合わせから成る群から選ばれることを特徴とする請求項1記載の組成物。
- 該少なくとも1種の表面活性剤は水の表面張力を低下させ得る1種またはそれ以上の表面活性剤を含んで成ることを特徴とする請求項1記載の組成物。
- 請求項1記載の農業用組成物を植生または土壌に接触させる段階を含んで成ることを特徴とする植生の処理方法。
- 請求項1記載の農業用組成物を基質に接触させる段階を含んで成ることを特徴とする基質の処理方法。
- (a)少なくとも1種の窒素含有イセチオン酸塩、および
(b)少なくとも1種の表面活性剤
を含んで成ることを特徴とする農業用助剤。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US17239809P | 2009-04-24 | 2009-04-24 | |
US61/172,398 | 2009-04-24 | ||
PCT/US2010/032146 WO2010124151A1 (en) | 2009-04-24 | 2010-04-23 | Nitrogen containing isethionic acid salts in field ready spray and tank mixes |
Publications (3)
Publication Number | Publication Date |
---|---|
JP2012524812A true JP2012524812A (ja) | 2012-10-18 |
JP2012524812A5 JP2012524812A5 (ja) | 2013-05-16 |
JP5576475B2 JP5576475B2 (ja) | 2014-08-20 |
Family
ID=43011492
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012507404A Expired - Fee Related JP5602834B2 (ja) | 2009-04-24 | 2010-04-23 | 登録し得る安定な農業用調合物中における窒素含有イセチオン酸塩 |
JP2012507403A Expired - Fee Related JP5576475B2 (ja) | 2009-04-24 | 2010-04-23 | フィールド・レディ・スプレーおよびタンク混合物中における窒素含有イセチオン酸塩 |
Family Applications Before (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2012507404A Expired - Fee Related JP5602834B2 (ja) | 2009-04-24 | 2010-04-23 | 登録し得る安定な農業用調合物中における窒素含有イセチオン酸塩 |
Country Status (10)
Country | Link |
---|---|
US (2) | US8859464B2 (ja) |
EP (2) | EP2421821B1 (ja) |
JP (2) | JP5602834B2 (ja) |
CN (2) | CN102414167B (ja) |
AU (2) | AU2010238686B2 (ja) |
BR (2) | BRPI1014594A2 (ja) |
CA (2) | CA2759702C (ja) |
ES (2) | ES2603327T3 (ja) |
MX (2) | MX342473B (ja) |
WO (2) | WO2010124151A1 (ja) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CA2830518C (en) * | 2011-04-20 | 2019-07-16 | Huntsman Petrochemical Llc | Spray drift reduction agents comprising low hydrophilic-lipophilic balance surfactants |
CN113973799A (zh) * | 2021-10-12 | 2022-01-28 | 广东海洋大学 | 羟乙基磺酸在清除吸附型底栖硅藻中的应用 |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001158770A (ja) * | 1999-12-02 | 2001-06-12 | Asahi Denka Kogyo Kk | ヒドロキシアルカンスルホン酸脂肪酸エステル類 |
JP2010518126A (ja) * | 2007-02-12 | 2010-05-27 | アーチャー・ダニエルズ・ミッドランド カンパニー | アジュバントおよびそれらを使用する方法 |
Family Cites Families (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2913324A (en) * | 1955-05-16 | 1959-11-17 | Monsanto Chemicals | Sulfoethyl carboxylic acid ester plant growth regulants |
US3408174A (en) * | 1962-12-10 | 1968-10-29 | Witco Chemical Corp | Dispersant compositions and toxicant concentrates containing the same |
US3692512A (en) * | 1969-06-03 | 1972-09-19 | Norman Henry Sachnik | Controlling agricultural chemical spray drift with foam |
US3799758A (en) | 1971-08-09 | 1974-03-26 | Monsanto Co | N-phosphonomethyl-glycine phytotoxicant compositions |
US3951842A (en) | 1973-04-02 | 1976-04-20 | Lever Brothers Company | Synthetic detergent bar with antimushing agent |
IL65187A (en) | 1982-03-08 | 1985-03-31 | Geshuri Lab Ltd | N-phosphonomethylglycine derivatives,processes for their preparation and herbicidal compositions containing them |
US4571309A (en) * | 1983-07-20 | 1986-02-18 | Westvaco Corporation | C22 -Cycloaliphatic tricarboxylic acid derived isethionate esters and method of preparation |
US5229424A (en) * | 1988-11-16 | 1993-07-20 | The Wellcome Foundation Limited | Pesticidal cyclopropyl 2,4-dieneamides |
US5646320A (en) * | 1993-10-28 | 1997-07-08 | Henkel Corporation | Process for making isethionate ester salts |
US5523432A (en) | 1994-04-07 | 1996-06-04 | Henkel Kommanditgesellschaft Auf Aktien | Process for the production of quaternary ammonium salts of fatty acid hydroxyalkanesulfonic acids |
DE19511460A1 (de) * | 1995-03-29 | 1996-10-02 | Hoechst Ag | Verfahren zur Herstellung von Acyloxyalkansulfonaten mit verbesserten Eigenschaften |
DE19511459A1 (de) * | 1995-03-29 | 1996-10-02 | Hoechst Ag | Verfahren zur Herstellung von Acyloxyalkansulfonaten mit verbesserten Eigenschaften |
US7423167B2 (en) | 1997-01-28 | 2008-09-09 | Stepan Company | Ethylenically unsaturated amine salts of sulfonic, phosphoric and carboxylic acids |
CA2320305A1 (en) | 1998-02-13 | 1999-08-19 | Monsanto Company | Storage-stable composition containing exogenous chemical substance and siloxane surfactant |
DE69920035T2 (de) | 1998-11-23 | 2005-09-15 | Monsanto Technology Llc. | Hochkonzentrierte wässrige glyphosatzusammensetzungen |
CA2459698C (en) * | 2001-09-07 | 2010-02-23 | Syngenta Participations Ag | Surfactant systems for agriculturally active compounds |
US20040138064A1 (en) * | 2002-11-13 | 2004-07-15 | Tann R Scott | Adjuvant for water soluble herbicides |
CN102792969B (zh) * | 2005-03-04 | 2015-01-21 | 孟山都技术公司 | 减轻用除草剂草甘膦制剂处理的草甘膦耐受性转基因棉花植物内的坏死 |
PL2300420T3 (pl) | 2008-07-21 | 2014-02-28 | Cognis Ip Man Gmbh | Siarczany alkoholi wielowodorotlenowych, polioli, sacharydów i polisacharydów do zastosowań rolniczych |
-
2010
- 2010-04-23 CN CN201080017821.6A patent/CN102414167B/zh not_active Expired - Fee Related
- 2010-04-23 CA CA2759702A patent/CA2759702C/en not_active Expired - Fee Related
- 2010-04-23 MX MX2011011120A patent/MX342473B/es active IP Right Grant
- 2010-04-23 JP JP2012507404A patent/JP5602834B2/ja not_active Expired - Fee Related
- 2010-04-23 CN CN201080017822.0A patent/CN102413689B/zh not_active Expired - Fee Related
- 2010-04-23 BR BRPI1014594-0A patent/BRPI1014594A2/pt active Search and Examination
- 2010-04-23 BR BRPI1015337-3A patent/BRPI1015337A2/pt not_active Application Discontinuation
- 2010-04-23 US US13/264,465 patent/US8859464B2/en not_active Expired - Fee Related
- 2010-04-23 WO PCT/US2010/032146 patent/WO2010124151A1/en active Application Filing
- 2010-04-23 MX MX2011011203A patent/MX2011011203A/es active IP Right Grant
- 2010-04-23 EP EP10767808.8A patent/EP2421821B1/en not_active Not-in-force
- 2010-04-23 CA CA2759265A patent/CA2759265C/en not_active Expired - Fee Related
- 2010-04-23 ES ES10767807.0T patent/ES2603327T3/es active Active
- 2010-04-23 WO PCT/US2010/032147 patent/WO2010124152A1/en active Application Filing
- 2010-04-23 US US13/264,470 patent/US8883685B2/en not_active Expired - Fee Related
- 2010-04-23 ES ES10767808.8T patent/ES2639226T3/es active Active
- 2010-04-23 AU AU2010238686A patent/AU2010238686B2/en not_active Ceased
- 2010-04-23 JP JP2012507403A patent/JP5576475B2/ja not_active Expired - Fee Related
- 2010-04-23 AU AU2010238687A patent/AU2010238687B2/en not_active Ceased
- 2010-04-23 EP EP10767807.0A patent/EP2421365B1/en not_active Not-in-force
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2001158770A (ja) * | 1999-12-02 | 2001-06-12 | Asahi Denka Kogyo Kk | ヒドロキシアルカンスルホン酸脂肪酸エステル類 |
JP2010518126A (ja) * | 2007-02-12 | 2010-05-27 | アーチャー・ダニエルズ・ミッドランド カンパニー | アジュバントおよびそれらを使用する方法 |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
RU2190329C2 (ru) | Гербицидные композиции, способ уничтожения или подавления сорняков или нежелательных растений | |
AU2008363855B2 (en) | A liquid, homogenous herbicide composition, a method of weed control, a method of production of liquid, homogenous herbicide composition and use of a liquid, homogenous herbicide composition for weed control | |
US20080103047A1 (en) | Herbicidal Composition Comprising an Aminophosphate or Aminophosphonate Salt, a Betaine and an Amine Oxide | |
JP2014139199A (ja) | 農業用の窒素含有界面活性剤 | |
JP5576475B2 (ja) | フィールド・レディ・スプレーおよびタンク混合物中における窒素含有イセチオン酸塩 | |
JP4323800B2 (ja) | 除草剤組成物 | |
US9271488B2 (en) | Isethionic acid salts in field ready spray and tank mixes | |
AU2010276088B2 (en) | Cocoalkylpolyamine alkoxylates as agents for high strength herbicide compositions | |
RU2446684C2 (ru) | Поверхностно-активные алкиламидопропилдиалкиламины в качестве адъювантов | |
BR112012006016A2 (pt) | fórmulação de pesticida e método para prover proteção de pesticidas a uma cultura agrícola |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20130326 |
|
A621 | Written request for application examination |
Free format text: JAPANESE INTERMEDIATE CODE: A621 Effective date: 20130326 |
|
A977 | Report on retrieval |
Free format text: JAPANESE INTERMEDIATE CODE: A971007 Effective date: 20140303 |
|
A131 | Notification of reasons for refusal |
Free format text: JAPANESE INTERMEDIATE CODE: A131 Effective date: 20140305 |
|
A521 | Request for written amendment filed |
Free format text: JAPANESE INTERMEDIATE CODE: A523 Effective date: 20140602 |
|
TRDD | Decision of grant or rejection written | ||
A01 | Written decision to grant a patent or to grant a registration (utility model) |
Free format text: JAPANESE INTERMEDIATE CODE: A01 Effective date: 20140625 |
|
A61 | First payment of annual fees (during grant procedure) |
Free format text: JAPANESE INTERMEDIATE CODE: A61 Effective date: 20140703 |
|
R150 | Certificate of patent or registration of utility model |
Ref document number: 5576475 Country of ref document: JP Free format text: JAPANESE INTERMEDIATE CODE: R150 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
R250 | Receipt of annual fees |
Free format text: JAPANESE INTERMEDIATE CODE: R250 |
|
LAPS | Cancellation because of no payment of annual fees |