ZA200306491B - Novel fungicide compositions based on pyridylmethylbenzamide and propamocarb derivative. - Google Patents
Novel fungicide compositions based on pyridylmethylbenzamide and propamocarb derivative. Download PDFInfo
- Publication number
- ZA200306491B ZA200306491B ZA200306491A ZA200306491A ZA200306491B ZA 200306491 B ZA200306491 B ZA 200306491B ZA 200306491 A ZA200306491 A ZA 200306491A ZA 200306491 A ZA200306491 A ZA 200306491A ZA 200306491 B ZA200306491 B ZA 200306491B
- Authority
- ZA
- South Africa
- Prior art keywords
- compound
- radical
- fungicidal compositions
- compositions according
- optionally substituted
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 78
- 230000000855 fungicidal effect Effects 0.000 title claims description 38
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical class CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 title claims description 12
- 239000000417 fungicide Substances 0.000 title description 2
- 150000001875 compounds Chemical class 0.000 claims description 83
- -1 substituted alkyl radical Chemical class 0.000 claims description 37
- 238000000034 method Methods 0.000 claims description 18
- 150000003839 salts Chemical class 0.000 claims description 18
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- 239000005821 Propamocarb Substances 0.000 claims description 10
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 10
- 230000002195 synergetic effect Effects 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 8
- 125000005843 halogen group Chemical group 0.000 claims description 8
- BLNWTAHYTCHDJH-UHFFFAOYSA-O hydroxy(oxo)azanium Chemical compound O[NH+]=O BLNWTAHYTCHDJH-UHFFFAOYSA-O 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
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- SOQBVABWOPYFQZ-UHFFFAOYSA-N oxygen(2-);titanium(4+) Chemical class [O-2].[O-2].[Ti+4] SOQBVABWOPYFQZ-UHFFFAOYSA-N 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 230000007170 pathology Effects 0.000 description 1
- OGYFATSSENRIKG-UHFFFAOYSA-N pencycuron Chemical compound C1=CC(Cl)=CC=C1CN(C(=O)NC=1C=CC=CC=1)C1CCCC1 OGYFATSSENRIKG-UHFFFAOYSA-N 0.000 description 1
- WBTYBAGIHOISOQ-UHFFFAOYSA-N pent-4-en-1-yl 2-[(2-furylmethyl)(imidazol-1-ylcarbonyl)amino]butanoate Chemical compound C1=CN=CN1C(=O)N(C(CC)C(=O)OCCCC=C)CC1=CC=CO1 WBTYBAGIHOISOQ-UHFFFAOYSA-N 0.000 description 1
- 230000000361 pesticidal effect Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- IEQIEDJGQAUEQZ-UHFFFAOYSA-N phthalocyanine Chemical compound N1C(N=C2C3=CC=CC=C3C(N=C3C4=CC=CC=C4C(=N4)N3)=N2)=C(C=CC=C2)C2=C1N=C1C2=CC=CC=C2C4=N1 IEQIEDJGQAUEQZ-UHFFFAOYSA-N 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
- 239000010773 plant oil Substances 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920002689 polyvinyl acetate Polymers 0.000 description 1
- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920002451 polyvinyl alcohol Polymers 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 230000003449 preventive effect Effects 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
- 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
- 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
- 230000001681 protective effect Effects 0.000 description 1
- 229960003351 prussian blue Drugs 0.000 description 1
- 239000013225 prussian blue Substances 0.000 description 1
- 239000008262 pumice Substances 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
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 description 1
- XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- WRPIRSINYZBGPK-UHFFFAOYSA-N quinoxyfen Chemical compound C1=CC(F)=CC=C1OC1=CC=NC2=CC(Cl)=CC(Cl)=C12 WRPIRSINYZBGPK-UHFFFAOYSA-N 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite Nutrition 0.000 description 1
- 239000003352 sequestering agent Substances 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
- 239000002002 slurry Substances 0.000 description 1
- 238000001228 spectrum Methods 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
- 239000003381 stabilizer Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- XOAAWQZATWQOTB-UHFFFAOYSA-N taurine Chemical class NCCS(O)(=O)=O XOAAWQZATWQOTB-UHFFFAOYSA-N 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
- 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
- 229960004546 thiabendazole Drugs 0.000 description 1
- 235000010296 thiabendazole Nutrition 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 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
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-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
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- 239000013008 thixotropic agent Substances 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 239000011573 trace mineral Substances 0.000 description 1
- 235000013619 trace mineral Nutrition 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
- QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
- 229940078499 tricalcium phosphate Drugs 0.000 description 1
- 229910000391 tricalcium phosphate Inorganic materials 0.000 description 1
- 235000019731 tricalcium phosphate Nutrition 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
- 235000013311 vegetables Nutrition 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
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)
- Pyridine Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0103141A FR2821719B1 (fr) | 2001-03-08 | 2001-03-08 | Nouvelles compositions fongicides a base de derive de pyridylmethylbenzamide et de propamocarbe |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200306491B true ZA200306491B (en) | 2004-10-12 |
Family
ID=8860874
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200306491A ZA200306491B (en) | 2001-03-08 | 2003-08-20 | Novel fungicide compositions based on pyridylmethylbenzamide and propamocarb derivative. |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US7659292B2 (es) |
| EP (1) | EP1370141B1 (es) |
| JP (1) | JP4280072B2 (es) |
| KR (1) | KR100830387B1 (es) |
| CN (1) | CN1250080C (es) |
| AR (1) | AR035765A1 (es) |
| AT (1) | ATE286350T1 (es) |
| AU (1) | AU2002242777B2 (es) |
| BG (1) | BG66295B1 (es) |
| BR (1) | BR0208000B1 (es) |
| CA (1) | CA2441826C (es) |
| DE (1) | DE60202519T2 (es) |
| DK (1) | DK1370141T3 (es) |
| EG (1) | EG23207A (es) |
| ES (1) | ES2231671T3 (es) |
| FR (1) | FR2821719B1 (es) |
| HR (1) | HRP20030810B1 (es) |
| HU (1) | HU229497B1 (es) |
| IL (1) | IL157776A0 (es) |
| MX (1) | MXPA03008027A (es) |
| MY (1) | MY126236A (es) |
| NZ (1) | NZ528287A (es) |
| PL (1) | PL205570B1 (es) |
| PT (1) | PT1370141E (es) |
| RS (1) | RS51504B (es) |
| UA (1) | UA75912C2 (es) |
| WO (1) | WO2002069714A1 (es) |
| ZA (1) | ZA200306491B (es) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1311742C (zh) * | 2003-04-15 | 2007-04-25 | 拜尔农科股份有限公司 | 含吡啶基甲基苯甲酰胺衍生物和百菌清的杀真菌组合物 |
| ES2529047T3 (es) * | 2005-02-11 | 2015-02-16 | Bayer Intellectual Property Gmbh | Composición fungicida que comprende un derivado de piridilmetilbenzamida y un derivado de tiazolocarboxamida |
| CL2007003748A1 (es) * | 2006-12-22 | 2008-07-18 | Bayer Cropscience Ag | Composicion pesticida que comprende fosetil-al, propamocarb-hcl y una sustancia insecticida activa; y metodo para controlar hongos fitopatogenos o insecticidas daninos de las plantas, cultivos o semillas que comprende aplicar dicha composicion. |
| CL2007003745A1 (es) * | 2006-12-22 | 2008-07-11 | Bayer Cropscience Ag | Composicion pesticida que comprende fosetil-al, propamocarb-hcl y una sustancia insecticida activa; y metodo para controlar hongos fitopatogenos o insecticidas daninos de las plantas, cultivos o semillas que comprende aplicar dicha composicion. |
| CL2007003746A1 (es) * | 2006-12-22 | 2008-07-18 | Bayer Cropscience Ag | Composicion pesticida que comprende propamocarb-hcl y un compuesto insecticida; y metodo para controlar hongos fitopatogenos o insecticidas daninos de las plantas, cultivos o semillas que comprende aplicar dicha composicion. |
| CL2007003744A1 (es) * | 2006-12-22 | 2008-07-11 | Bayer Cropscience Ag | Composicion que comprende un derivado 2-piridilmetilbenzamida y un compuesto insecticida; y metodo para controlar de forma curativa o preventiva hongos fitopatogenos de cultivos e insectos. |
| GB0906515D0 (en) * | 2009-04-15 | 2009-05-20 | Syngenta Participations Ag | Fungical compositions |
| CN102342287A (zh) * | 2011-11-08 | 2012-02-08 | 陕西美邦农药有限公司 | 一种含氟吡菌胺与多抗霉素的杀菌组合物 |
| EP3279185B1 (en) | 2016-08-04 | 2018-11-14 | Taminco bvba | Improved process for the preparation of carbamates |
| CN112970760A (zh) * | 2021-02-24 | 2021-06-18 | 安徽科技学院 | 一种三元复配杀菌剂及其在小麦茎基腐病防治中的应用 |
| CN115943962B (zh) * | 2023-01-05 | 2024-06-25 | 河南科技学院 | 一种防治小麦纹枯病的杀菌组合物 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3915755A1 (de) | 1989-05-13 | 1990-11-29 | Bayer Ag | Fungizide mittel sowie substituierte aminosaeureamid-derivate und deren herstellung |
| DE4026966A1 (de) | 1990-08-25 | 1992-02-27 | Bayer Ag | Substituierte valinamid-derivate |
| WO1996004252A1 (fr) | 1994-08-03 | 1996-02-15 | Kumiai Chemical Industry Co., Ltd. | Derives amides aminoacides, procede d'obtention de ce derive, fongicide a usage agricole et horticole et procede de traitement fongicide |
| TW575562B (en) * | 1998-02-19 | 2004-02-11 | Agrevo Uk Ltd | Fungicides |
| TW200306155A (en) | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
-
2001
- 2001-03-08 FR FR0103141A patent/FR2821719B1/fr not_active Expired - Fee Related
-
2002
- 2002-02-19 NZ NZ528287A patent/NZ528287A/en not_active IP Right Cessation
- 2002-02-19 AT AT02708410T patent/ATE286350T1/de active
- 2002-02-19 ES ES02708410T patent/ES2231671T3/es not_active Expired - Lifetime
- 2002-02-19 EP EP02708410A patent/EP1370141B1/fr not_active Expired - Lifetime
- 2002-02-19 DK DK02708410T patent/DK1370141T3/da active
- 2002-02-19 BR BRPI0208000-1A patent/BR0208000B1/pt active IP Right Grant
- 2002-02-19 RS YUP-706/03A patent/RS51504B/en unknown
- 2002-02-19 US US10/471,125 patent/US7659292B2/en not_active Expired - Lifetime
- 2002-02-19 MX MXPA03008027A patent/MXPA03008027A/es active IP Right Grant
- 2002-02-19 WO PCT/FR2002/000621 patent/WO2002069714A1/fr active IP Right Grant
- 2002-02-19 AU AU2002242777A patent/AU2002242777B2/en not_active Expired
- 2002-02-19 CA CA2441826A patent/CA2441826C/fr not_active Expired - Lifetime
- 2002-02-19 UA UA2003109118A patent/UA75912C2/uk unknown
- 2002-02-19 JP JP2002568908A patent/JP4280072B2/ja not_active Expired - Lifetime
- 2002-02-19 HU HU0303420A patent/HU229497B1/hu unknown
- 2002-02-19 DE DE60202519T patent/DE60202519T2/de not_active Expired - Lifetime
- 2002-02-19 IL IL15777602A patent/IL157776A0/xx active IP Right Grant
- 2002-02-19 PT PT02708410T patent/PT1370141E/pt unknown
- 2002-02-19 PL PL362935A patent/PL205570B1/pl unknown
- 2002-02-19 KR KR1020037011827A patent/KR100830387B1/ko active IP Right Grant
- 2002-02-19 CN CNB028059891A patent/CN1250080C/zh not_active Expired - Lifetime
- 2002-03-05 EG EG20020238A patent/EG23207A/xx active
- 2002-03-06 MY MYPI20020798A patent/MY126236A/en unknown
- 2002-03-07 AR ARP020100834A patent/AR035765A1/es active IP Right Grant
-
2003
- 2003-08-20 ZA ZA200306491A patent/ZA200306491B/en unknown
- 2003-09-02 BG BG108148A patent/BG66295B1/bg unknown
- 2003-10-07 HR HR20030810A patent/HRP20030810B1/xx not_active IP Right Cessation
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