UA73131C2 - Herbicidal emulsifiable concentrated composition on the basis of dinitroaniline and oxyacetamide herbicides and a water mixture - Google Patents
Herbicidal emulsifiable concentrated composition on the basis of dinitroaniline and oxyacetamide herbicides and a water mixture Download PDFInfo
- Publication number
- UA73131C2 UA73131C2 UA2002010530A UA2002010530A UA73131C2 UA 73131 C2 UA73131 C2 UA 73131C2 UA 2002010530 A UA2002010530 A UA 2002010530A UA 2002010530 A UA2002010530 A UA 2002010530A UA 73131 C2 UA73131 C2 UA 73131C2
- Authority
- UA
- Ukraine
- Prior art keywords
- composition according
- composition
- herbicide
- alkyl
- oxyacetamide
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 77
- 239000004009 herbicide Substances 0.000 title claims abstract description 39
- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 25
- LZGUHMNOBNWABZ-UHFFFAOYSA-N n-nitro-n-phenylnitramide Chemical compound [O-][N+](=O)N([N+]([O-])=O)C1=CC=CC=C1 LZGUHMNOBNWABZ-UHFFFAOYSA-N 0.000 title claims abstract description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 title claims description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 claims abstract description 36
- 229910000147 aluminium phosphate Inorganic materials 0.000 claims abstract description 18
- 125000000217 alkyl group Chemical group 0.000 claims description 13
- 239000003960 organic solvent Substances 0.000 claims description 12
- 239000005591 Pendimethalin Substances 0.000 claims description 11
- 239000003995 emulsifying agent Substances 0.000 claims description 11
- CHIFOSRWCNZCFN-UHFFFAOYSA-N pendimethalin Chemical compound CCC(CC)NC1=C([N+]([O-])=O)C=C(C)C(C)=C1[N+]([O-])=O CHIFOSRWCNZCFN-UHFFFAOYSA-N 0.000 claims description 11
- 239000013530 defoamer Substances 0.000 claims description 10
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 8
- 238000009835 boiling Methods 0.000 claims description 7
- 239000002904 solvent Substances 0.000 claims description 7
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 claims description 6
- 125000001188 haloalkyl group Chemical group 0.000 claims description 6
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 6
- 229920001521 polyalkylene glycol ether Polymers 0.000 claims description 6
- 239000005531 Flufenacet Substances 0.000 claims description 5
- IANUJLZYFUDJIH-UHFFFAOYSA-N flufenacet Chemical compound C=1C=C(F)C=CC=1N(C(C)C)C(=O)COC1=NN=C(C(F)(F)F)S1 IANUJLZYFUDJIH-UHFFFAOYSA-N 0.000 claims description 5
- 125000001424 substituent group Chemical group 0.000 claims description 5
- -1 3,4-dimethylphenyl Chemical group 0.000 claims description 4
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims description 4
- 150000002191 fatty alcohols Chemical class 0.000 claims description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 3
- 229920001400 block copolymer Polymers 0.000 claims description 3
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 claims description 3
- YRIUSKIDOIARQF-UHFFFAOYSA-N dodecyl benzenesulfonate Chemical compound CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 YRIUSKIDOIARQF-UHFFFAOYSA-N 0.000 claims description 3
- 229940071161 dodecylbenzenesulfonate Drugs 0.000 claims description 3
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 claims description 3
- 125000004198 2-fluorophenyl group Chemical group [H]C1=C([H])C(F)=C(*)C([H])=C1[H] 0.000 claims description 2
- 125000004179 3-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C(Cl)=C1[H] 0.000 claims description 2
- 125000001255 4-fluorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1F 0.000 claims description 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 125000004186 cyclopropylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C1([H])[H] 0.000 claims description 2
- 125000004441 haloalkylsulfonyl group Chemical group 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 125000000040 m-tolyl group Chemical group [H]C1=C([H])C(*)=C([H])C(=C1[H])C([H])([H])[H] 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 125000003261 o-tolyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])C([H])([H])[H] 0.000 claims description 2
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 claims description 2
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 2
- 238000004683 secondary electrospray ionisation mass spectroscopy Methods 0.000 claims description 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims description 2
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 2
- 239000004215 Carbon black (E152) Substances 0.000 claims 1
- 125000003545 alkoxy group Chemical group 0.000 claims 1
- 125000002029 aromatic hydrocarbon group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 229930195733 hydrocarbon Natural products 0.000 claims 1
- 150000002430 hydrocarbons Chemical class 0.000 claims 1
- 238000012876 topography Methods 0.000 claims 1
- 230000015556 catabolic process Effects 0.000 abstract 1
- 238000006731 degradation reaction Methods 0.000 abstract 1
- 239000004495 emulsifiable concentrate Substances 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 239000000126 substance Substances 0.000 description 7
- 239000008240 homogeneous mixture Substances 0.000 description 6
- 229920005682 EO-PO block copolymer Polymers 0.000 description 5
- 238000000034 method Methods 0.000 description 5
- 239000000243 solution Substances 0.000 description 5
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 4
- OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 4
- 239000012141 concentrate Substances 0.000 description 4
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
- 238000002156 mixing Methods 0.000 description 4
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 2
- FZERHIULMFGESH-UHFFFAOYSA-N N-phenylacetamide Chemical compound CC(=O)NC1=CC=CC=C1 FZERHIULMFGESH-UHFFFAOYSA-N 0.000 description 2
- 241001441284 Zeidae Species 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 description 1
- 125000004521 1,3,4-thiadiazol-2-yl group Chemical group S1C(=NN=C1)* 0.000 description 1
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 1
- 229960001413 acetanilide Drugs 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 150000004657 carbamic acid derivatives Chemical class 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000010779 crude oil Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005194 fractionation Methods 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- BHEPBYXIRTUNPN-UHFFFAOYSA-N hydridophosphorus(.) (triplet) Chemical compound [PH] BHEPBYXIRTUNPN-UHFFFAOYSA-N 0.000 description 1
- 230000007062 hydrolysis Effects 0.000 description 1
- 238000006460 hydrolysis reaction Methods 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 125000005575 polycyclic aromatic hydrocarbon group Chemical group 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/22—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing ingredients stabilising the active ingredients
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
-
- 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N33/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds
- A01N33/16—Biocides, pest repellants or attractants, or plant growth regulators containing organic nitrogen compounds containing nitrogen-to-oxygen bonds
- A01N33/18—Nitro compounds
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)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33791199A | 1999-06-22 | 1999-06-22 | |
| PCT/US2000/016947 WO2000078148A1 (en) | 1999-06-22 | 2000-06-20 | Herbicidal emulsifiable concentrate compositions of dinitroaniline and oxyacetamide herbicides |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA73131C2 true UA73131C2 (en) | 2005-06-15 |
Family
ID=23322546
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA2002010530A UA73131C2 (en) | 1999-06-22 | 2000-06-20 | Herbicidal emulsifiable concentrated composition on the basis of dinitroaniline and oxyacetamide herbicides and a water mixture |
Country Status (25)
| Country | Link |
|---|---|
| EP (1) | EP1187532B1 (ru) |
| JP (1) | JP3845012B2 (ru) |
| KR (1) | KR100725197B1 (ru) |
| CN (1) | CN1173629C (ru) |
| AT (1) | ATE246451T1 (ru) |
| AU (1) | AU771385B2 (ru) |
| BG (1) | BG65113B1 (ru) |
| BR (1) | BR0011824A (ru) |
| CA (1) | CA2377304C (ru) |
| CZ (1) | CZ294499B6 (ru) |
| DE (1) | DE60004360T2 (ru) |
| DK (1) | DK1187532T3 (ru) |
| EA (1) | EA004575B1 (ru) |
| ES (1) | ES2204631T3 (ru) |
| GE (1) | GEP20053670B (ru) |
| HU (1) | HU225982B1 (ru) |
| IL (1) | IL146783A0 (ru) |
| MX (1) | MXPA01013360A (ru) |
| NZ (1) | NZ516073A (ru) |
| PL (1) | PL200929B1 (ru) |
| PT (1) | PT1187532E (ru) |
| SK (1) | SK284759B6 (ru) |
| UA (1) | UA73131C2 (ru) |
| WO (1) | WO2000078148A1 (ru) |
| ZA (1) | ZA200200495B (ru) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2011082957A2 (de) * | 2009-12-17 | 2011-07-14 | Bayer Cropscience Ag | Herbizide mittel enthaltend flufenacet |
| CN112741083A (zh) * | 2019-10-31 | 2021-05-04 | 江苏七洲绿色化工股份有限公司 | 一种氟乐灵乳油 |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2954396A (en) * | 1958-05-16 | 1960-09-27 | Pure Oil Co | Stabilization of carbamate esters |
| US5624884A (en) * | 1986-05-23 | 1997-04-29 | American Cyanamid Company | Aqueous suspension concentrate compositions of pendimethalin |
| DE3821600A1 (de) * | 1988-06-27 | 1989-12-28 | Bayer Ag | Heteroaryloxyessigsaeure-n-isopropylanilide |
| JP2562723B2 (ja) * | 1990-08-10 | 1996-12-11 | 三洋電機株式会社 | 冷媒組成物及び冷凍装置 |
| US5270286A (en) * | 1991-01-31 | 1993-12-14 | American Cyanamid Company | Herbicidal emulsifiable concentrate compositions of imidazolinone herbicides |
| DE4223465A1 (de) * | 1992-07-16 | 1994-01-20 | Bayer Ag | Herbizide Mittel auf Basis von Heteroaryloxyacetamiden |
| ES2128984B1 (es) * | 1996-05-24 | 2000-02-01 | Bayer Ag | Herbicidas a base de heteroariloxi-acetamidas para el empleo en el cultivo de arroz. |
| US6071858A (en) * | 1997-12-12 | 2000-06-06 | Bayer Corporation | Stable, dry compositions for use as herbicides |
-
2000
- 2000-06-20 GE GE4678A patent/GEP20053670B/en unknown
- 2000-06-20 AT AT00941576T patent/ATE246451T1/de active
- 2000-06-20 AU AU56267/00A patent/AU771385B2/en not_active Expired
- 2000-06-20 IL IL14678300A patent/IL146783A0/xx active IP Right Grant
- 2000-06-20 KR KR1020017016397A patent/KR100725197B1/ko not_active IP Right Cessation
- 2000-06-20 UA UA2002010530A patent/UA73131C2/uk unknown
- 2000-06-20 SK SK1823-2001A patent/SK284759B6/sk not_active IP Right Cessation
- 2000-06-20 EP EP00941576A patent/EP1187532B1/en not_active Expired - Lifetime
- 2000-06-20 ES ES00941576T patent/ES2204631T3/es not_active Expired - Lifetime
- 2000-06-20 DK DK00941576T patent/DK1187532T3/da active
- 2000-06-20 DE DE60004360T patent/DE60004360T2/de not_active Expired - Lifetime
- 2000-06-20 HU HU0202153A patent/HU225982B1/hu not_active IP Right Cessation
- 2000-06-20 PT PT00941576T patent/PT1187532E/pt unknown
- 2000-06-20 BR BR0011824-9A patent/BR0011824A/pt not_active Application Discontinuation
- 2000-06-20 MX MXPA01013360A patent/MXPA01013360A/es active IP Right Grant
- 2000-06-20 PL PL352906A patent/PL200929B1/pl unknown
- 2000-06-20 NZ NZ516073A patent/NZ516073A/en not_active IP Right Cessation
- 2000-06-20 WO PCT/US2000/016947 patent/WO2000078148A1/en active IP Right Grant
- 2000-06-20 CZ CZ20014615A patent/CZ294499B6/cs not_active IP Right Cessation
- 2000-06-20 EA EA200200043A patent/EA004575B1/ru not_active IP Right Cessation
- 2000-06-20 CA CA002377304A patent/CA2377304C/en not_active Expired - Fee Related
- 2000-06-20 JP JP2001504228A patent/JP3845012B2/ja not_active Expired - Lifetime
- 2000-06-20 CN CNB008093237A patent/CN1173629C/zh not_active Expired - Lifetime
-
2001
- 2001-12-20 BG BG106256A patent/BG65113B1/bg unknown
-
2002
- 2002-01-21 ZA ZA200200495A patent/ZA200200495B/xx unknown
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