UA80792C2 - Fungicidal mixture which contains derivative of triazolopyrimidine and dodine, agent and method for controlling fungi patogenous to rice, seeds - Google Patents
Fungicidal mixture which contains derivative of triazolopyrimidine and dodine, agent and method for controlling fungi patogenous to rice, seeds Download PDFInfo
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- UA80792C2 UA80792C2 UAA200612855A UAA200612855A UA80792C2 UA 80792 C2 UA80792 C2 UA 80792C2 UA A200612855 A UAA200612855 A UA A200612855A UA A200612855 A UAA200612855 A UA A200612855A UA 80792 C2 UA80792 C2 UA 80792C2
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- compound
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- rice
- mixture
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- 239000000203 mixture Substances 0.000 title claims abstract description 49
- 235000007164 Oryza sativa Nutrition 0.000 title claims abstract description 16
- 235000009566 rice Nutrition 0.000 title claims abstract description 16
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 13
- 238000000034 method Methods 0.000 title claims abstract description 11
- YWBFPKPWMSWWEA-UHFFFAOYSA-O triazolopyrimidine Chemical class BrC1=CC=CC(C=2N=C3N=CN[N+]3=C(NCC=3C=CN=CC=3)C=2)=C1 YWBFPKPWMSWWEA-UHFFFAOYSA-O 0.000 title claims abstract description 6
- YIKWKLYQRFRGPM-UHFFFAOYSA-N 1-dodecylguanidine acetate Chemical compound CC(O)=O.CCCCCCCCCCCCN=C(N)N YIKWKLYQRFRGPM-UHFFFAOYSA-N 0.000 title claims abstract description 5
- 240000007594 Oryza sativa Species 0.000 title claims abstract 3
- 241000233866 Fungi Species 0.000 title claims description 6
- 239000005766 Dodine Substances 0.000 title abstract 2
- 239000003795 chemical substances by application Substances 0.000 title description 3
- 150000001875 compounds Chemical class 0.000 claims abstract description 53
- 239000000417 fungicide Substances 0.000 claims abstract description 16
- HTSGKJQDMSTCGS-UHFFFAOYSA-N 1,4-bis(4-chlorophenyl)-2-(4-methylphenyl)sulfonylbutane-1,4-dione Chemical compound C1=CC(C)=CC=C1S(=O)(=O)C(C(=O)C=1C=CC(Cl)=CC=1)CC(=O)C1=CC=C(Cl)C=C1 HTSGKJQDMSTCGS-UHFFFAOYSA-N 0.000 claims abstract 2
- 241000196324 Embryophyta Species 0.000 claims description 17
- 244000053095 fungal pathogen Species 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 7
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- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- AMQJEAYHLZJPGS-UHFFFAOYSA-N N-Pentanol Chemical compound CCCCCO AMQJEAYHLZJPGS-UHFFFAOYSA-N 0.000 description 2
- UFWIBTONFRDIAS-UHFFFAOYSA-N Naphthalene Chemical compound C1=CC=CC2=CC=CC=C21 UFWIBTONFRDIAS-UHFFFAOYSA-N 0.000 description 2
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- OSGAYBCDTDRGGQ-UHFFFAOYSA-L calcium sulfate Chemical compound [Ca+2].[O-]S([O-])(=O)=O OSGAYBCDTDRGGQ-UHFFFAOYSA-L 0.000 description 2
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- YPHMISFOHDHNIV-FSZOTQKASA-N cycloheximide Chemical compound C1[C@@H](C)C[C@H](C)C(=O)[C@@H]1[C@H](O)CC1CC(=O)NC(=O)C1 YPHMISFOHDHNIV-FSZOTQKASA-N 0.000 description 2
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- CKAPSXZOOQJIBF-UHFFFAOYSA-N hexachlorobenzene Chemical compound ClC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl CKAPSXZOOQJIBF-UHFFFAOYSA-N 0.000 description 2
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- LQDARGUHUSPFNL-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)-3-(1,1,2,2-tetrafluoroethoxy)propyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(COC(F)(F)C(F)F)CN1C=NC=N1 LQDARGUHUSPFNL-UHFFFAOYSA-N 0.000 description 1
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- 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
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 238000000655 nuclear magnetic resonance spectrum Methods 0.000 description 1
- 239000010742 number 1 fuel oil Substances 0.000 description 1
- UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 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
- 239000012188 paraffin wax Substances 0.000 description 1
- LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
- 239000000575 pesticide Substances 0.000 description 1
- 229940044654 phenolsulfonic acid Drugs 0.000 description 1
- IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 229920002635 polyurethane Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 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
- QXJKBPAVAHBARF-BETUJISGSA-N procymidone Chemical compound O=C([C@]1(C)C[C@@]1(C1=O)C)N1C1=CC(Cl)=CC(Cl)=C1 QXJKBPAVAHBARF-BETUJISGSA-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
- 230000001681 protective effect Effects 0.000 description 1
- HZRSNVGNWUDEFX-UHFFFAOYSA-N pyraclostrobin Chemical compound COC(=O)N(OC)C1=CC=CC=C1COC1=NN(C=2C=CC(Cl)=CC=2)C=C1 HZRSNVGNWUDEFX-UHFFFAOYSA-N 0.000 description 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-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
- 235000012239 silicon dioxide Nutrition 0.000 description 1
- MXMXHPPIGKYTAR-UHFFFAOYSA-N silthiofam Chemical compound CC=1SC([Si](C)(C)C)=C(C(=O)NCC=C)C=1C MXMXHPPIGKYTAR-UHFFFAOYSA-N 0.000 description 1
- 239000004550 soluble concentrate 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
- 239000007921 spray Substances 0.000 description 1
- 238000001694 spray drying Methods 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 230000002195 synergetic effect Effects 0.000 description 1
- 230000009885 systemic effect Effects 0.000 description 1
- LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 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
- WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 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
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-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
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-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
- 150000003672 ureas Chemical class 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 239000002023 wood Substances 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
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)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Catching Or Destruction (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102004023160 | 2004-05-07 | ||
| PCT/EP2005/004481 WO2005112642A1 (de) | 2004-05-07 | 2005-04-27 | Fungizide mischungen zur bekämpfung von reispathogenen |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA80792C2 true UA80792C2 (en) | 2007-10-25 |
Family
ID=35063223
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UAA200612855A UA80792C2 (en) | 2004-05-07 | 2005-04-27 | Fungicidal mixture which contains derivative of triazolopyrimidine and dodine, agent and method for controlling fungi patogenous to rice, seeds |
Country Status (21)
| Country | Link |
|---|---|
| US (1) | US20070208039A1 (zh) |
| EP (1) | EP1746891A1 (zh) |
| JP (1) | JP2007536304A (zh) |
| KR (1) | KR20070007959A (zh) |
| CN (1) | CN1949974A (zh) |
| AR (1) | AR048779A1 (zh) |
| AU (1) | AU2005245260A1 (zh) |
| BR (1) | BRPI0510544A (zh) |
| CA (1) | CA2562635A1 (zh) |
| CR (1) | CR8707A (zh) |
| EA (1) | EA200602012A1 (zh) |
| IL (1) | IL178559A0 (zh) |
| MX (1) | MXPA06011750A (zh) |
| NO (1) | NO20065507L (zh) |
| NZ (1) | NZ550841A (zh) |
| PE (1) | PE20060111A1 (zh) |
| TW (1) | TW200539806A (zh) |
| UA (1) | UA80792C2 (zh) |
| UY (1) | UY28888A1 (zh) |
| WO (1) | WO2005112642A1 (zh) |
| ZA (1) | ZA200610179B (zh) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2507746C2 (ru) * | 2008-07-03 | 2014-02-27 | Исихара Сангио Кайся, Лтд. | Фунгицидная композиция и способ контроля болезней растений |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2867562A (en) * | 1956-06-26 | 1959-01-06 | American Cyanamid Co | Dodecylguanidine salts as fruit tree fungicides |
| US5593996A (en) * | 1991-12-30 | 1997-01-14 | American Cyanamid Company | Triazolopyrimidine derivatives |
| EP0643538B1 (en) * | 1993-09-09 | 1999-03-17 | Sony Corporation | Motion vector detecting apparatus and method |
| TWI252231B (en) * | 1997-04-14 | 2006-04-01 | American Cyanamid Co | Fungicidal trifluorophenyl-triazolopyrimidines |
| FR2777747B1 (fr) * | 1998-04-27 | 2000-07-28 | Rhone Poulenc Agrochimie | Composition fongicide et/ou bactericide synergique |
| US6268371B1 (en) * | 1998-09-10 | 2001-07-31 | American Cyanamid Co. | Fungicidal mixtures |
| SI0988790T1 (en) * | 1998-09-25 | 2003-10-31 | Basf Aktiengesellschaft | Fungicidal mixtures |
-
2005
- 2005-04-27 BR BRPI0510544-7A patent/BRPI0510544A/pt not_active IP Right Cessation
- 2005-04-27 KR KR1020067025649A patent/KR20070007959A/ko not_active Application Discontinuation
- 2005-04-27 CN CNA2005800146002A patent/CN1949974A/zh active Pending
- 2005-04-27 NZ NZ550841A patent/NZ550841A/en unknown
- 2005-04-27 CA CA002562635A patent/CA2562635A1/en not_active Abandoned
- 2005-04-27 AU AU2005245260A patent/AU2005245260A1/en not_active Abandoned
- 2005-04-27 WO PCT/EP2005/004481 patent/WO2005112642A1/de active Application Filing
- 2005-04-27 JP JP2007511954A patent/JP2007536304A/ja not_active Withdrawn
- 2005-04-27 UA UAA200612855A patent/UA80792C2/uk unknown
- 2005-04-27 EP EP05741772A patent/EP1746891A1/de not_active Withdrawn
- 2005-04-27 EA EA200602012A patent/EA200602012A1/ru unknown
- 2005-04-27 US US11/579,662 patent/US20070208039A1/en not_active Abandoned
- 2005-04-27 MX MXPA06011750A patent/MXPA06011750A/es not_active Application Discontinuation
- 2005-05-03 PE PE2005000492A patent/PE20060111A1/es not_active Application Discontinuation
- 2005-05-06 AR ARP050101853A patent/AR048779A1/es not_active Application Discontinuation
- 2005-05-06 UY UY28888A patent/UY28888A1/es unknown
- 2005-05-06 TW TW094114622A patent/TW200539806A/zh unknown
-
2006
- 2006-10-15 IL IL178559A patent/IL178559A0/en unknown
- 2006-10-25 CR CR8707A patent/CR8707A/es not_active Application Discontinuation
- 2006-11-29 NO NO20065507A patent/NO20065507L/no not_active Application Discontinuation
- 2006-12-05 ZA ZA200610179A patent/ZA200610179B/xx unknown
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2507746C2 (ru) * | 2008-07-03 | 2014-02-27 | Исихара Сангио Кайся, Лтд. | Фунгицидная композиция и способ контроля болезней растений |
| US8962661B2 (en) | 2008-07-03 | 2015-02-24 | Ishihara Sangyo Kaisha, Ltd. | Fungicidal composition and method for controlling plant diseases |
Also Published As
| Publication number | Publication date |
|---|---|
| CN1949974A (zh) | 2007-04-18 |
| WO2005112642A1 (de) | 2005-12-01 |
| CR8707A (es) | 2007-08-28 |
| US20070208039A1 (en) | 2007-09-06 |
| NO20065507L (no) | 2006-01-12 |
| EA200602012A1 (ru) | 2007-08-31 |
| ZA200610179B (en) | 2008-09-25 |
| UY28888A1 (es) | 2005-11-30 |
| JP2007536304A (ja) | 2007-12-13 |
| AU2005245260A1 (en) | 2005-12-01 |
| TW200539806A (en) | 2005-12-16 |
| EP1746891A1 (de) | 2007-01-31 |
| CA2562635A1 (en) | 2005-12-01 |
| IL178559A0 (en) | 2007-02-11 |
| NZ550841A (en) | 2009-05-31 |
| AR048779A1 (es) | 2006-05-24 |
| MXPA06011750A (es) | 2007-03-26 |
| PE20060111A1 (es) | 2006-04-07 |
| BRPI0510544A (pt) | 2007-10-30 |
| KR20070007959A (ko) | 2007-01-16 |
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