UA77972C2 - Фунгицидная композиция, содержащая производное пиридилметилбензамида и производное дитиокарбамата, способ лечения или предотвращения появления фитопатогенных грибов на сельскохозяйственных культурах - Google Patents
Фунгицидная композиция, содержащая производное пиридилметилбензамида и производное дитиокарбамата, способ лечения или предотвращения появления фитопатогенных грибов на сельскохозяйственных культурах Download PDFInfo
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- UA77972C2 UA77972C2 UA20040402996A UA20040402996A UA77972C2 UA 77972 C2 UA77972 C2 UA 77972C2 UA 20040402996 A UA20040402996 A UA 20040402996A UA 20040402996 A UA20040402996 A UA 20040402996A UA 77972 C2 UA77972 C2 UA 77972C2
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- crops
- fungicidal
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- powdery mildew
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 229910052750 molybdenum Inorganic materials 0.000 description 1
- 239000011733 molybdenum Substances 0.000 description 1
- 229910052901 montmorillonite Inorganic materials 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 229940042880 natural phospholipid Drugs 0.000 description 1
- 239000005645 nematicide Substances 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 239000004535 oil miscible liquid Substances 0.000 description 1
- 125000005968 oxazolinyl group Chemical group 0.000 description 1
- CFHIDWOYWUOIHU-UHFFFAOYSA-N oxomethyl Chemical compound O=[CH] CFHIDWOYWUOIHU-UHFFFAOYSA-N 0.000 description 1
- 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
- 235000012736 patent blue V Nutrition 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
- 239000000575 pesticide Substances 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- 150000002989 phenols Chemical class 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
- 235000021110 pickles Nutrition 0.000 description 1
- 239000006187 pill Substances 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
- 239000004584 polyacrylic acid Substances 0.000 description 1
- 238000006068 polycondensation reaction Methods 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
- WHHIPMZEDGBUCC-UHFFFAOYSA-N probenazole Chemical compound C1=CC=C2C(OCC=C)=NS(=O)(=O)C2=C1 WHHIPMZEDGBUCC-UHFFFAOYSA-N 0.000 description 1
- WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-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
- 230000001681 protective effect Effects 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
- 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
- 235000021013 raspberries Nutrition 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000002829 reductive effect Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 239000005871 repellent Substances 0.000 description 1
- 230000002940 repellent Effects 0.000 description 1
- 230000001850 reproductive effect Effects 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 239000011435 rock Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 238000007790 scraping Methods 0.000 description 1
- 229910052624 sepiolite Inorganic materials 0.000 description 1
- 235000019355 sepiolite 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
- 239000004509 smoke generator Substances 0.000 description 1
- 239000004550 soluble concentrate Substances 0.000 description 1
- 239000002904 solvent 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
- 239000004575 stone Substances 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229920001059 synthetic polymer Polymers 0.000 description 1
- 235000020357 syrup Nutrition 0.000 description 1
- 239000006188 syrup Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 235000012222 talc Nutrition 0.000 description 1
- 229940104261 taurate Drugs 0.000 description 1
- 238000012360 testing method Methods 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
- 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
- 230000009974 thixotropic effect Effects 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 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
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 239000004552 water soluble powder Substances 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 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
Abstract
Синергическая фунгицидная композиция, содержащая: (a) производное пиридилметилбензамида формулы (І), в которой различные радикалы имеют значения, указанные в описании, и (b) соединение (II), которое представляет собой производное дитиокарбамата, имеющее фунгицидную активность и выбранное из группы, которая включает фербам, манкопер, манкозеб, манеб, метирам, набам, никель бис(диметилдитиокарбамат), пропинеб и цинеб, и их приемлемые, с точки зрения сельского хозяйства, изомеры и с присоединением солей кислоты, а также способ для лечебного и предупредительного контроля фитопатогенных грибов сельскохозяйственных культур, включающий применение эффективного и нефитотоксичного количества одной из этих фунгицидных композиций.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0113688A FR2831022B1 (fr) | 2001-10-23 | 2001-10-23 | Composition fongicide a base d'au moins un derive de pyridylmethylbenzamide et d'au moins un derive dithiocarbamate |
PCT/EP2002/013789 WO2003034824A1 (en) | 2001-10-23 | 2002-10-21 | Fungicidal composition based on at least one pyridylmethylbenzamide derivative and at least one dithiocarbamate derivative |
Publications (1)
Publication Number | Publication Date |
---|---|
UA77972C2 true UA77972C2 (ru) | 2007-02-15 |
Family
ID=8868622
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA20040402996A UA77972C2 (ru) | 2001-10-23 | 2002-10-21 | Фунгицидная композиция, содержащая производное пиридилметилбензамида и производное дитиокарбамата, способ лечения или предотвращения появления фитопатогенных грибов на сельскохозяйственных культурах |
Country Status (25)
Country | Link |
---|---|
US (1) | US7326725B2 (ru) |
EP (1) | EP1437939B1 (ru) |
JP (1) | JP4698949B2 (ru) |
KR (1) | KR100975251B1 (ru) |
CN (1) | CN1301645C (ru) |
AR (1) | AR037246A1 (ru) |
AT (1) | ATE313951T1 (ru) |
BR (2) | BR0213673B1 (ru) |
CA (1) | CA2466798C (ru) |
CO (1) | CO5580721A2 (ru) |
DE (1) | DE60208417T2 (ru) |
DK (1) | DK1437939T3 (ru) |
EG (1) | EG23301A (ru) |
ES (1) | ES2254788T3 (ru) |
FR (1) | FR2831022B1 (ru) |
IL (2) | IL161008A0 (ru) |
MX (1) | MXPA04003756A (ru) |
MY (1) | MY136602A (ru) |
PE (1) | PE20030517A1 (ru) |
PL (1) | PL206247B1 (ru) |
RU (1) | RU2292137C2 (ru) |
TW (1) | TWI235036B (ru) |
UA (1) | UA77972C2 (ru) |
WO (1) | WO2003034824A1 (ru) |
ZA (1) | ZA200402815B (ru) |
Families Citing this family (13)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
TW200306155A (en) | 2002-03-19 | 2003-11-16 | Du Pont | Benzamides and advantageous compositions thereof for use as fungicides |
EP1527683A1 (en) * | 2003-10-31 | 2005-05-04 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylmethylbenzamide derivative and a sulfamide derivative |
US9215874B2 (en) * | 2005-02-11 | 2015-12-22 | Thomas Wegmann | Fungicidal composition comprising a pyridylmethylbenzamide derivative and a thiazolecarboxamide derivative |
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. |
CN102308821B (zh) * | 2007-10-15 | 2013-11-27 | 张少武 | 一种含有代森联的有效成分的杀菌剂组合物 |
CN101180962B (zh) * | 2007-12-17 | 2012-04-04 | 东莞市瑞德丰生物科技有限公司 | 含有中生菌素和代森锌的具有增效作用的组合物 |
US20100143502A1 (en) * | 2008-12-09 | 2010-06-10 | Roger Rolland Ellis | Plant wash |
CN101971840A (zh) * | 2010-11-22 | 2011-02-16 | 陕西美邦农药有限公司 | 一种含环唑醇与代森联的杀菌组合物 |
CN102369939A (zh) * | 2011-10-28 | 2012-03-14 | 陕西美邦农药有限公司 | 一种含氟吡菌胺与硫代氨基甲酸酯类化合物的杀菌组合物 |
CN103120169A (zh) * | 2011-11-18 | 2013-05-29 | 深圳诺普信农化股份有限公司 | 一种含有氟吡菌胺的杀菌组合物 |
CN103155932A (zh) * | 2013-03-27 | 2013-06-19 | 北京燕化永乐农药有限公司 | 杀菌组合物 |
ES2910071T3 (es) | 2018-03-08 | 2022-05-11 | Incyte Corp | Compuestos de aminopirazina diol como inhibidores de PI3K-Y |
WO2020010003A1 (en) | 2018-07-02 | 2020-01-09 | Incyte Corporation | AMINOPYRAZINE DERIVATIVES AS PI3K-γ INHIBITORS |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0613442B2 (ja) * | 1985-06-25 | 1994-02-23 | 石原産業株式会社 | 農園芸用殺菌剤組成物 |
JPH01102006A (ja) * | 1987-10-16 | 1989-04-19 | Mitsui Toatsu Chem Inc | 農園芸用殺菌組成物 |
JP2648621B2 (ja) * | 1988-08-08 | 1997-09-03 | 三井東圧化学株式会社 | 農園芸用殺菌組成物 |
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 |
JPH07157403A (ja) * | 1993-12-02 | 1995-06-20 | Sumitomo Chem Co Ltd | 殺菌剤組成物 |
BR9508472A (pt) | 1994-08-03 | 1997-10-28 | Kumiai Chemical Industry Co | Derivados amida de aminoácido processo para preparação dos mesmos fungicidas para agricultura ou horticultura e método para mater fungos |
JPH09175911A (ja) * | 1995-12-26 | 1997-07-08 | Ube Ind Ltd | 農園芸用の殺菌剤組成物 |
JP3818771B2 (ja) * | 1998-02-12 | 2006-09-06 | 三井化学株式会社 | 植物病害防除剤組成物 |
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
- 2001-10-23 FR FR0113688A patent/FR2831022B1/fr not_active Expired - Fee Related
-
2002
- 2002-10-14 PE PE2002001010A patent/PE20030517A1/es active IP Right Grant
- 2002-10-18 TW TW091124077A patent/TWI235036B/zh not_active IP Right Cessation
- 2002-10-21 BR BRPI0213673-2B1A patent/BR0213673B1/pt active IP Right Grant
- 2002-10-21 AT AT02801920T patent/ATE313951T1/de active
- 2002-10-21 ES ES02801920T patent/ES2254788T3/es not_active Expired - Lifetime
- 2002-10-21 CN CNB028207254A patent/CN1301645C/zh not_active Expired - Lifetime
- 2002-10-21 EP EP02801920A patent/EP1437939B1/en not_active Expired - Lifetime
- 2002-10-21 DE DE60208417T patent/DE60208417T2/de not_active Expired - Lifetime
- 2002-10-21 BR BRPI0213673A patent/BRPI0213673A8/pt unknown
- 2002-10-21 PL PL368538A patent/PL206247B1/pl unknown
- 2002-10-21 CA CA2466798A patent/CA2466798C/en not_active Expired - Lifetime
- 2002-10-21 KR KR1020047005776A patent/KR100975251B1/ko active IP Right Grant
- 2002-10-21 MY MYPI20023915A patent/MY136602A/en unknown
- 2002-10-21 DK DK02801920T patent/DK1437939T3/da active
- 2002-10-21 US US10/493,591 patent/US7326725B2/en not_active Expired - Lifetime
- 2002-10-21 MX MXPA04003756A patent/MXPA04003756A/es active IP Right Grant
- 2002-10-21 UA UA20040402996A patent/UA77972C2/ru unknown
- 2002-10-21 JP JP2003537403A patent/JP4698949B2/ja not_active Expired - Lifetime
- 2002-10-21 WO PCT/EP2002/013789 patent/WO2003034824A1/en active IP Right Grant
- 2002-10-21 RU RU2004115620/04A patent/RU2292137C2/ru active
- 2002-10-21 IL IL16100802A patent/IL161008A0/xx active IP Right Grant
- 2002-10-22 EG EG2002101157A patent/EG23301A/xx active
- 2002-10-22 AR ARP020103987A patent/AR037246A1/es active IP Right Grant
-
2004
- 2004-03-22 IL IL161008A patent/IL161008A/en unknown
- 2004-04-13 ZA ZA2004/02815A patent/ZA200402815B/en unknown
- 2004-05-18 CO CO04045825A patent/CO5580721A2/es active IP Right Grant
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