ES2342633T3 - Procedimiento para la intensificacion de la eficacia de ethaboxam. - Google Patents
Procedimiento para la intensificacion de la eficacia de ethaboxam. Download PDFInfo
- Publication number
- ES2342633T3 ES2342633T3 ES08154087T ES08154087T ES2342633T3 ES 2342633 T3 ES2342633 T3 ES 2342633T3 ES 08154087 T ES08154087 T ES 08154087T ES 08154087 T ES08154087 T ES 08154087T ES 2342633 T3 ES2342633 T3 ES 2342633T3
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- ethaboxam
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- PVTHJAPFENJVNC-MHRBZPPQSA-N kasugamycin Chemical compound N[C@H]1C[C@H](NC(=N)C(O)=O)[C@@H](C)O[C@@H]1O[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H]1O PVTHJAPFENJVNC-MHRBZPPQSA-N 0.000 description 1
- 239000003350 kerosene Substances 0.000 description 1
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- BCTQJXQXJVLSIG-UHFFFAOYSA-N mepronil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C)=C1 BCTQJXQXJVLSIG-UHFFFAOYSA-N 0.000 description 1
- XWPZUHJBOLQNMN-UHFFFAOYSA-N metconazole Chemical compound C1=NC=NN1CC1(O)C(C)(C)CCC1CC1=CC=C(Cl)C=C1 XWPZUHJBOLQNMN-UHFFFAOYSA-N 0.000 description 1
- ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 description 1
- CJPQIRJHIZUAQP-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(phenylacetyl)alaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)CC1=CC=CC=C1 CJPQIRJHIZUAQP-UHFFFAOYSA-N 0.000 description 1
- HIIRDDUVRXCDBN-OBGWFSINSA-N metominostrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1OC1=CC=CC=C1 HIIRDDUVRXCDBN-OBGWFSINSA-N 0.000 description 1
- AMSPWOYQQAWRRM-UHFFFAOYSA-N metrafenone Chemical compound COC1=CC=C(Br)C(C)=C1C(=O)C1=C(C)C=C(OC)C(OC)=C1OC AMSPWOYQQAWRRM-UHFFFAOYSA-N 0.000 description 1
- 238000007392 microtiter assay Methods 0.000 description 1
- 238000005497 microtitration Methods 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- UQJQVUOTMVCFHX-UHFFFAOYSA-L nabam Chemical compound [Na+].[Na+].[S-]C(=S)NCCNC([S-])=S UQJQVUOTMVCFHX-UHFFFAOYSA-L 0.000 description 1
- 150000002790 naphthalenes Chemical class 0.000 description 1
- 229960003255 natamycin Drugs 0.000 description 1
- NCXMLFZGDNKEPB-FFPOYIOWSA-N natamycin Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]2O[C@@H]2C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 NCXMLFZGDNKEPB-FFPOYIOWSA-N 0.000 description 1
- 239000004311 natamycin Substances 0.000 description 1
- 235000010298 natamycin Nutrition 0.000 description 1
- 125000006501 nitrophenyl group Chemical group 0.000 description 1
- 229920000847 nonoxynol Polymers 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical class CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 235000015097 nutrients Nutrition 0.000 description 1
- AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 description 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 description 1
- 239000003973 paint Substances 0.000 description 1
- 239000000123 paper Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 244000045947 parasite Species 0.000 description 1
- 230000001717 pathogenic effect Effects 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 238000003359 percent control normalization Methods 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- LFGREXWGYUGZLY-UHFFFAOYSA-N phosphoryl Chemical group [P]=O LFGREXWGYUGZLY-UHFFFAOYSA-N 0.000 description 1
- 229920001983 poloxamer Polymers 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001083 polybutene Polymers 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000193 polymethacrylate Polymers 0.000 description 1
- YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920002223 polystyrene Polymers 0.000 description 1
- 239000004814 polyurethane Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 235000019422 polyvinyl alcohol Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 1
- TVLSRXXIMLFWEO-UHFFFAOYSA-N prochloraz Chemical compound C1=CN=CN1C(=O)N(CCC)CCOC1=C(Cl)C=C(Cl)C=C1Cl TVLSRXXIMLFWEO-UHFFFAOYSA-N 0.000 description 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- STJLVHWMYQXCPB-UHFFFAOYSA-N propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 description 1
- KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 description 1
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- 150000004040 pyrrolidinones Chemical class 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- 235000012239 silicon dioxide Nutrition 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
- 238000001694 spray drying Methods 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 150000003450 sulfenic acids Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- 239000004308 thiabendazole Substances 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
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 229960004546 thiabendazole Drugs 0.000 description 1
- 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
- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-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
- 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
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 239000004562 water dispersible granule Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 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
- A01N43/72—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
- A01N43/74—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 one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
- A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
Applications Claiming Priority (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004057070 | 2004-11-25 | ||
| DE102004057070 | 2004-11-25 | ||
| DE102004058585 | 2004-12-03 | ||
| DE102004058585 | 2004-12-03 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2342633T3 true ES2342633T3 (es) | 2010-07-09 |
Family
ID=35709358
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES08154087T Active ES2342633T3 (es) | 2004-11-25 | 2005-11-23 | Procedimiento para la intensificacion de la eficacia de ethaboxam. |
Country Status (21)
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2008189658A (ja) | 2007-01-12 | 2008-08-21 | Nissan Chem Ind Ltd | 植物病害の防除方法 |
| TWI526535B (zh) * | 2008-09-12 | 2016-03-21 | 住友化學股份有限公司 | 噻唑菌胺對於基因轉殖植物在植物病害之防治方法的用途 |
| JP5365159B2 (ja) * | 2008-11-25 | 2013-12-11 | 住友化学株式会社 | 有害生物防除用組成物及び有害生物の防除方法 |
| JP5359224B2 (ja) | 2008-11-25 | 2013-12-04 | 住友化学株式会社 | 植物病害防除用組成物及び植物病害の防除方法 |
| JP5365161B2 (ja) * | 2008-11-25 | 2013-12-11 | 住友化学株式会社 | 植物病害防除用組成物及び植物病害の防除方法 |
| JP5359223B2 (ja) * | 2008-11-25 | 2013-12-04 | 住友化学株式会社 | 植物病害防除用組成物及び植物病害の防除方法 |
| AR075573A1 (es) * | 2009-02-11 | 2011-04-20 | Basf Se | Dimethomorph como protector de plaguicidas con efectos fitotoxicos |
| KR101800907B1 (ko) | 2010-01-06 | 2017-11-23 | 스미또모 가가꾸 가부시끼가이샤 | 해충 방제용 조성물 및 방법 |
| JP5857509B2 (ja) * | 2011-08-03 | 2016-02-10 | 住友化学株式会社 | 植物病害防除組成物およびその用途 |
| CN104066326A (zh) * | 2012-01-25 | 2014-09-24 | 住友化学株式会社 | 植物病害防治组合物 |
| EP2622961A1 (en) * | 2012-02-02 | 2013-08-07 | Bayer CropScience AG | Acive compound combinations |
| CN103385245B (zh) * | 2012-05-11 | 2016-05-18 | 陕西韦尔奇作物保护有限公司 | 一种含噻酰菌胺与硫代氨基甲酸酯类的杀菌组合物 |
| CN103688950A (zh) * | 2013-12-10 | 2014-04-02 | 济南凯因生物科技有限公司 | 防治番茄晚疫病的组合物 |
| CN104186511A (zh) * | 2014-08-20 | 2014-12-10 | 石家庄市深泰化工有限公司 | 一种含有吡唑醚菌酯和噻唑菌胺的杀菌组合物 |
| KR20180082603A (ko) | 2015-12-01 | 2018-07-18 | 스미또모 가가꾸 가부시끼가이샤 | 식물 병해 방제 조성물 및 식물 병해 방제 방법 |
Family Cites Families (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2504404A (en) | 1946-06-12 | 1950-04-18 | Du Pont | Manganous ethylene bis-dithiocarbamate and fungicidal compositions containing same |
| NL254917A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1954-07-28 | |||
| DE1076434B (de) | 1957-08-17 | 1960-02-25 | Badische Anilin- S. Soda-Fabrik Aktiengesellschaft, Ludwigshafen/Rhein | Fungizide Mittel |
| CH351791A (de) | 1957-10-26 | 1961-01-31 | Merck Ag E | Fungizides Mittel |
| NL277376A (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1961-05-09 | |||
| NL129620C (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) | 1963-04-01 | |||
| US4512969A (en) | 1974-09-17 | 1985-04-23 | Eastman Kodak Company | Compositions containing hydrophobic addenda uniformly loaded in latex polymer particles |
| CS244440B2 (en) | 1983-02-28 | 1986-07-17 | Celamerck Gmbh & Co Kg | Method of acrylic acids' new amides production |
| DE3623921A1 (de) | 1986-07-16 | 1988-01-21 | Basf Ag | Oximether und diese enthaltende fungizide |
| US5514643A (en) | 1993-08-16 | 1996-05-07 | Lucky Ltd. | 2-aminothiazolecarboxamide derivatives, processes for preparing the same and use thereof for controlling phytopathogenic organisms |
| DE4423612A1 (de) | 1994-07-06 | 1996-01-11 | Basf Ag | 2-[(Dihydro)pyrazolyl-3'-oxymethylen]-anilide, Verfahren zu ihrer Herstelung und ihre Verwendung |
| US5723491A (en) | 1994-07-11 | 1998-03-03 | Novartis Corporation | Fungicidal composition and method of controlling fungus infestation |
| DE69718288T2 (de) | 1997-02-21 | 2003-07-31 | Shenyang Research Institute Of Chemical Industry, Shenyang Liaoning | Fluorine enthaltende Diphenylacrylamid Microbizide |
| TWI252231B (en) | 1997-04-14 | 2006-04-01 | American Cyanamid Co | Fungicidal trifluorophenyl-triazolopyrimidines |
| GT199800109A (es) | 1997-08-06 | 2000-01-13 | Derivados de n-sulfonilglicinalquiniloxifenetilamida microbicidas. | |
| CN1212768C (zh) * | 1999-12-13 | 2005-08-03 | 拜尔公司 | 杀真菌活性化合物的组合 |
| DE10019758A1 (de) * | 2000-04-20 | 2001-10-25 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| KR100426179B1 (ko) | 2000-05-10 | 2004-04-03 | 주식회사 엘지생명과학 | Ｎ-(α-시아노-2-테닐)-4-에틸-2-(에틸아미노)-5-티아졸카르복사미드를 함유하는 신규한 살균제 조성물 |
| DE10141618A1 (de) * | 2001-08-24 | 2003-03-06 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| ES2304549T3 (es) * | 2002-12-06 | 2008-10-16 | Dow Agrosciences Llc | Composiciones sinergicas. |
-
2005
- 2005-11-11 PE PE2005001320A patent/PE20060796A1/es not_active Application Discontinuation
- 2005-11-23 EP EP05811186A patent/EP1816914A1/de not_active Withdrawn
- 2005-11-23 EP EP10171034A patent/EP2255636A1/de not_active Withdrawn
- 2005-11-23 JP JP2007541831A patent/JP2008521761A/ja not_active Withdrawn
- 2005-11-23 CN CN200580040465A patent/CN100591207C/zh not_active Expired - Fee Related
- 2005-11-23 BR BRPI0518585-8A patent/BRPI0518585A2/pt not_active IP Right Cessation
- 2005-11-23 AU AU2005308946A patent/AU2005308946A1/en not_active Abandoned
- 2005-11-23 CN CN200910265699A patent/CN101743987A/zh active Pending
- 2005-11-23 EP EP10171032A patent/EP2255635A1/de not_active Withdrawn
- 2005-11-23 EP EP10171018A patent/EP2255631A1/de not_active Withdrawn
- 2005-11-23 KR KR1020077014305A patent/KR20070086584A/ko not_active Withdrawn
- 2005-11-23 PL PL08154087T patent/PL1949788T3/pl unknown
- 2005-11-23 AT AT08154087T patent/ATE463162T1/de not_active IP Right Cessation
- 2005-11-23 US US11/791,191 patent/US20080200334A1/en not_active Abandoned
- 2005-11-23 EP EP10171023A patent/EP2255632A1/de not_active Withdrawn
- 2005-11-23 EP EP10171029A patent/EP2255634A1/de not_active Withdrawn
- 2005-11-23 WO PCT/EP2005/012528 patent/WO2006056417A1/de active Application Filing
- 2005-11-23 CA CA002586441A patent/CA2586441A1/en not_active Abandoned
- 2005-11-23 MX MX2007005510A patent/MX2007005510A/es unknown
- 2005-11-23 EP EP10171025A patent/EP2255633A1/de not_active Withdrawn
- 2005-11-23 EP EP08154087A patent/EP1949788B1/de active Active
- 2005-11-23 EP EP09176984A patent/EP2206432A3/de not_active Withdrawn
- 2005-11-23 DE DE502005009390T patent/DE502005009390D1/de active Active
- 2005-11-23 ES ES08154087T patent/ES2342633T3/es active Active
- 2005-11-24 AR ARP050104917A patent/AR051777A1/es unknown
- 2005-11-25 TW TW094141601A patent/TW200631501A/zh unknown
- 2005-11-25 UY UY29229A patent/UY29229A1/es unknown
-
2007
- 2007-05-23 IN IN1845KO2007 patent/IN2007KO01845A/en unknown
- 2007-05-23 CR CR9145A patent/CR9145A/es not_active Application Discontinuation
- 2007-05-29 ZA ZA200704386A patent/ZA200704386B/xx unknown
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