UA109566C2 - Стабільні агрохічні масляні дисперсії - Google Patents
Стабільні агрохічні масляні дисперсії Download PDFInfo
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- UA109566C2 UA109566C2 UAA201310895A UAA201310895A UA109566C2 UA 109566 C2 UA109566 C2 UA 109566C2 UA A201310895 A UAA201310895 A UA A201310895A UA A201310895 A UAA201310895 A UA A201310895A UA 109566 C2 UA109566 C2 UA 109566C2
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- 239000004480 active ingredient Substances 0.000 claims abstract description 48
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- YGBMMMOLNODPBP-GWGZPXPZSA-N s-ethyl (2e,4e)-11-methoxy-3,7,11-trimethyldodeca-2,4-dienethioate Chemical compound CCSC(=O)\C=C(/C)\C=C\CC(C)CCCC(C)(C)OC YGBMMMOLNODPBP-GWGZPXPZSA-N 0.000 description 1
- NMFAMPYSJHIYMR-UHFFFAOYSA-N s-ethyl n-[3-(dimethylamino)propyl]carbamothioate;hydrochloride Chemical compound [Cl-].CCSC(=O)NCCC[NH+](C)C NMFAMPYSJHIYMR-UHFFFAOYSA-N 0.000 description 1
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 1
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- PTLRDCMBXHILCL-UHFFFAOYSA-M sodium arsenite Chemical compound [Na+].[O-][As]=O PTLRDCMBXHILCL-UHFFFAOYSA-M 0.000 description 1
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- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- VGTPCRGMBIAPIM-UHFFFAOYSA-M sodium thiocyanate Chemical compound [Na+].[S-]C#N VGTPCRGMBIAPIM-UHFFFAOYSA-M 0.000 description 1
- HCJLVWUMMKIQIM-UHFFFAOYSA-M sodium;2,3,4,5,6-pentachlorophenolate Chemical compound [Na+].[O-]C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl HCJLVWUMMKIQIM-UHFFFAOYSA-M 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- 239000008247 solid mixture Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
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- HXJUTPCZVOIRIF-UHFFFAOYSA-N sulfolane Chemical compound O=S1(=O)CCCC1 HXJUTPCZVOIRIF-UHFFFAOYSA-N 0.000 description 1
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- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003457 sulfones Chemical class 0.000 description 1
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- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000006228 supernatant Substances 0.000 description 1
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- 230000008961 swelling Effects 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
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- 239000002641 tar oil Substances 0.000 description 1
- UOORRWUZONOOLO-UHFFFAOYSA-N telone II Natural products ClCC=CCl UOORRWUZONOOLO-UHFFFAOYSA-N 0.000 description 1
- 239000002424 termiticide Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- 239000004308 thiabendazole Substances 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- WJCNZQLZVWNLKY-UHFFFAOYSA-N thiabendazole Chemical compound S1C=NC(C=2NC3=CC=CC=C3N=2)=C1 WJCNZQLZVWNLKY-UHFFFAOYSA-N 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- BAKXBZPQTXCKRR-UHFFFAOYSA-N thiodicarb Chemical compound CSC(C)=NOC(=O)NSNC(=O)ON=C(C)SC BAKXBZPQTXCKRR-UHFFFAOYSA-N 0.000 description 1
- OPASCBHCTNRLRM-UHFFFAOYSA-N thiometon Chemical compound CCSCCSP(=S)(OC)OC OPASCBHCTNRLRM-UHFFFAOYSA-N 0.000 description 1
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- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- ILERPRJWJPJZDN-UHFFFAOYSA-N thioquinox Chemical compound C1=CC=C2N=C(SC(=S)S3)C3=NC2=C1 ILERPRJWJPJZDN-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
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- 229940074152 thuringiensin Drugs 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- WPALTCMYPARVNV-UHFFFAOYSA-N tolfenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(OC=3C=CC(C)=CC=3)=CC=2)=C1Cl WPALTCMYPARVNV-UHFFFAOYSA-N 0.000 description 1
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-UHFFFAOYSA-N 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ONCZDRURRATYFI-TVJDWZFNSA-N trifloxystrobin Chemical compound CO\N=C(\C(=O)OC)C1=CC=CC=C1CO\N=C(/C)C1=CC=CC(C(F)(F)F)=C1 ONCZDRURRATYFI-TVJDWZFNSA-N 0.000 description 1
- HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- 239000005943 zeta-Cypermethrin 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
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Dispersion Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
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PCT/US2011/024457 WO2012108873A1 (en) | 2011-02-11 | 2011-02-11 | Stable agrochemical oil dispersions |
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UA109566C2 true UA109566C2 (xx) | 2015-09-10 |
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UAA201310895A UA109566C2 (xx) | 2011-02-11 | 2011-11-02 | Стабільні агрохічні масляні дисперсії |
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EP (1) | EP2672825A4 (es) |
JP (1) | JP5927207B2 (es) |
CN (1) | CN103501613B (es) |
AU (1) | AU2011358608B2 (es) |
BR (1) | BR112013020309B1 (es) |
CA (1) | CA2826867C (es) |
IL (1) | IL227888A (es) |
MX (1) | MX368933B (es) |
NZ (1) | NZ613876A (es) |
RU (1) | RU2562670C2 (es) |
UA (1) | UA109566C2 (es) |
WO (1) | WO2012108873A1 (es) |
ZA (1) | ZA201305943B (es) |
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US9321734B2 (en) | 2012-12-28 | 2016-04-26 | Dow Agrosciences Llc | N-(substituted)-5-fluoro-4-imino-3-methyl-2-oxo-3,4-dihydropyrimidine-1(2H)-carboxamide derivatives |
AU2013370470B2 (en) | 2012-12-28 | 2018-05-10 | Adama Makhteshim Ltd. | 1-(substituted-benzoyl)-5-fluoro-4-imino-3-methyl-3,4-dihydropyrimidin-2(1H)-one derivatives |
JP6324994B2 (ja) | 2012-12-28 | 2018-05-16 | アダマ・マクテシム・リミテッド | N−(置換)−5−フルオロ−4−イミノ−3−メチル−2−オキソ−3,4−ジヒドロピリミジン−1(2h)−カルボキシレート誘導体 |
WO2014105845A1 (en) | 2012-12-31 | 2014-07-03 | Dow Agrosciences Llc | 3-alkyl-5-fluoro-4-substituted-imino-3,4-dihydropyrimidin-2(1h)-one derivatives as fungicides |
BR102013009504A2 (pt) * | 2013-04-18 | 2015-03-17 | Oxiteno S A Indústria E Comércio | Formulação agroquímica do tipo dispersão em óleo, uso das formulações agroquímicas do tipo dispersão em óleo e processo de obtenção de formulação agroquímica do tipo dispersão em óleo |
CN103202290B (zh) * | 2013-05-07 | 2014-04-16 | 中化化工科学技术研究总院 | 氰氟草酯悬浮剂及其制备方法 |
EP2839744A1 (en) | 2013-08-23 | 2015-02-25 | Fine Agrochemicals Limited | Growth regulator concentrate and use thereof |
CN103931631A (zh) * | 2014-03-16 | 2014-07-23 | 广东中迅农科股份有限公司 | 一种含有精噁唑禾草灵和啶磺草胺的除草组合物 |
CN105557717B (zh) * | 2016-03-03 | 2018-08-03 | 江苏丰山集团股份有限公司 | 一种双氟磺草胺悬浮剂及其制备方法 |
PL3593637T3 (pl) | 2018-07-11 | 2024-04-02 | Fine Agrochemicals Limited | Koncentrat regulatora wzrostu roślin i jego zastosowanie |
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JPS4925136A (es) * | 1972-06-26 | 1974-03-06 | ||
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JPH0645521B2 (ja) * | 1985-01-21 | 1994-06-15 | イーシー化学株式会社 | 土壌に散布する殺虫殺菌剤用展着剤組成物 |
JPS61243007A (ja) * | 1985-04-22 | 1986-10-29 | Nippon Ekishiyou Kk | 膠化殺虫剤及びその製造方法 |
JPH0723285B2 (ja) * | 1986-02-20 | 1995-03-15 | イ−シ−化学工業株式会社 | 固型化薬剤の製造方法 |
JPH0644993B2 (ja) * | 1989-04-19 | 1994-06-15 | 三笠化学工業株式会社 | 水性懸濁状組成物 |
ES2073326T3 (es) * | 1992-01-28 | 1995-08-01 | Ishihara Sangyo Kaisha | Suspension herbicida a base de aceite quimicamente estabilizada. |
JPH07267809A (ja) * | 1994-03-30 | 1995-10-17 | Sds Biotech Kk | 蒸散性殺虫剤 |
JP2000247810A (ja) * | 1999-02-26 | 2000-09-12 | Meiji Seika Kaisha Ltd | 農薬の薬理効果促進剤 |
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GB0318448D0 (en) * | 2003-08-06 | 2003-09-10 | Syngenta Ltd | Formulation |
TWI396505B (zh) | 2006-01-13 | 2013-05-21 | Dow Agrosciences Llc | 2-(聚-經取代芳基)-6-胺-5-鹵-4-嘧啶羧酸及其作為除草劑之用途 |
KR101350071B1 (ko) | 2006-01-13 | 2014-01-14 | 다우 아그로사이언시즈 엘엘씨 | 6-(다-치환 아릴)-4-아미노피콜리네이트 및 그의제초제로서의 용도 |
US7662978B2 (en) | 2006-04-24 | 2010-02-16 | Milliken & Company | Dibenzylidene sorbitol (DBS)-based compounds, compositions and methods for using such compounds |
EP2040555A2 (en) * | 2006-05-10 | 2009-04-01 | E.I. Du Pont De Nemours And Company | Formulated tick and insect repellent compositions |
GB0712884D0 (en) * | 2007-07-03 | 2007-08-15 | Syngenta Ltd | Formulations |
JP5494906B2 (ja) * | 2008-10-24 | 2014-05-21 | 大日本除蟲菊株式会社 | 機能性グリコールゲル |
UA107670C2 (en) * | 2009-08-07 | 2015-02-10 | Dow Agrosciences Llc | Meso-sized capsules useful for the delivery of agricultural chemicals |
NZ597644A (en) * | 2009-08-07 | 2014-05-30 | Dow Agrosciences Llc | N1-sulfonyl-5-fluoropyrimidinone derivatives |
CN101897339B (zh) * | 2010-08-20 | 2013-09-11 | 陕西上格之路生物科学有限公司 | 一种含醚磺隆和五氟磺草胺的除草剂组合物 |
-
2011
- 2011-02-11 EP EP11858415.0A patent/EP2672825A4/en not_active Withdrawn
- 2011-02-11 AU AU2011358608A patent/AU2011358608B2/en not_active Ceased
- 2011-02-11 CA CA2826867A patent/CA2826867C/en not_active Expired - Fee Related
- 2011-02-11 NZ NZ61387611A patent/NZ613876A/en not_active IP Right Cessation
- 2011-02-11 CN CN201180070041.2A patent/CN103501613B/zh not_active Expired - Fee Related
- 2011-02-11 MX MX2013009259A patent/MX368933B/es active IP Right Grant
- 2011-02-11 WO PCT/US2011/024457 patent/WO2012108873A1/en active Application Filing
- 2011-02-11 BR BR112013020309-9A patent/BR112013020309B1/pt not_active IP Right Cessation
- 2011-02-11 RU RU2013141539/13A patent/RU2562670C2/ru not_active IP Right Cessation
- 2011-02-11 JP JP2013553408A patent/JP5927207B2/ja not_active Expired - Fee Related
- 2011-11-02 UA UAA201310895A patent/UA109566C2/uk unknown
-
2013
- 2013-08-07 ZA ZA2013/05943A patent/ZA201305943B/en unknown
- 2013-08-08 IL IL227888A patent/IL227888A/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
BR112013020309B1 (pt) | 2019-05-28 |
JP2014505100A (ja) | 2014-02-27 |
BR112013020309A2 (pt) | 2016-07-12 |
RU2013141539A (ru) | 2015-03-20 |
EP2672825A1 (en) | 2013-12-18 |
EP2672825A4 (en) | 2014-09-10 |
WO2012108873A1 (en) | 2012-08-16 |
JP5927207B2 (ja) | 2016-06-01 |
AU2011358608B2 (en) | 2016-04-14 |
CA2826867A1 (en) | 2012-08-16 |
RU2562670C2 (ru) | 2015-09-10 |
CN103501613A (zh) | 2014-01-08 |
CN103501613B (zh) | 2017-06-13 |
AU2011358608A1 (en) | 2013-08-22 |
MX2013009259A (es) | 2013-12-09 |
CA2826867C (en) | 2019-03-12 |
MX368933B (es) | 2019-10-22 |
ZA201305943B (en) | 2014-10-29 |
IL227888A (en) | 2017-01-31 |
NZ613876A (en) | 2015-03-27 |
IL227888A0 (en) | 2013-09-30 |
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