SK287383B6 - Fungicídne zmesi a spôsob kontroly škodlivých plesní - Google Patents
Fungicídne zmesi a spôsob kontroly škodlivých plesní Download PDFInfo
- Publication number
- SK287383B6 SK287383B6 SK904-2003A SK9042003A SK287383B6 SK 287383 B6 SK287383 B6 SK 287383B6 SK 9042003 A SK9042003 A SK 9042003A SK 287383 B6 SK287383 B6 SK 287383B6
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- SK
- Slovakia
- Prior art keywords
- methyl
- iii
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- ppm
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- 239000000203 mixture Substances 0.000 title claims abstract description 78
- 241000233866 Fungi Species 0.000 title claims abstract description 18
- 230000000855 fungicidal effect Effects 0.000 title claims abstract description 12
- 238000000034 method Methods 0.000 title claims abstract description 8
- 230000001473 noxious effect Effects 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 claims abstract description 101
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- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000000460 chlorine Substances 0.000 claims description 54
- -1 chloro, methyl Chemical group 0.000 claims description 44
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 36
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- 150000002367 halogens Chemical class 0.000 claims description 7
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- 239000010941 cobalt Substances 0.000 description 1
- GUTLYIVDDKVIGB-UHFFFAOYSA-N cobalt atom Chemical compound [Co] GUTLYIVDDKVIGB-UHFFFAOYSA-N 0.000 description 1
- 235000016213 coffee Nutrition 0.000 description 1
- 235000013353 coffee beverage Nutrition 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 235000005822 corn Nutrition 0.000 description 1
- 244000038559 crop plants Species 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- MNNHAPBLZZVQHP-UHFFFAOYSA-N diammonium hydrogen phosphate Chemical compound [NH4+].[NH4+].OP([O-])([O-])=O MNNHAPBLZZVQHP-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000002270 dispersing agent Substances 0.000 description 1
- LQZZUXJYWNFBMV-UHFFFAOYSA-N dodecan-1-ol Chemical compound CCCCCCCCCCCCO LQZZUXJYWNFBMV-UHFFFAOYSA-N 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
- 229910000514 dolomite Inorganic materials 0.000 description 1
- 230000009977 dual effect Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 235000013312 flour Nutrition 0.000 description 1
- 230000002538 fungal effect Effects 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 238000004128 high performance liquid chromatography Methods 0.000 description 1
- 229910000042 hydrogen bromide Inorganic materials 0.000 description 1
- 229910000041 hydrogen chloride Inorganic materials 0.000 description 1
- IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
- 229910000040 hydrogen fluoride Inorganic materials 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- 229910000043 hydrogen iodide Inorganic materials 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 238000007689 inspection Methods 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 229910052742 iron Inorganic materials 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 239000006028 limestone Substances 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 239000000395 magnesium oxide Substances 0.000 description 1
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 description 1
- WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical compound [Mn+2].[S-]C(=S)NCCNC([S-])=S.COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC WPBNNNQJVZRUHP-UHFFFAOYSA-L 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
- 229920000609 methyl cellulose Polymers 0.000 description 1
- WBYWAXJHAXSJNI-UHFFFAOYSA-N methyl p-hydroxycinnamate Natural products OC(=O)C=CC1=CC=CC=C1 WBYWAXJHAXSJNI-UHFFFAOYSA-N 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical class C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 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
- 235000014571 nuts Nutrition 0.000 description 1
- 229920002114 octoxynol-9 Polymers 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 1
- 239000006072 paste Substances 0.000 description 1
- 235000020232 peanut Nutrition 0.000 description 1
- 229920000570 polyether Polymers 0.000 description 1
- 229920001451 polypropylene glycol Polymers 0.000 description 1
- 235000019260 propionic acid Nutrition 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
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- 229960004889 salicylic acid Drugs 0.000 description 1
- 238000007873 sieving Methods 0.000 description 1
- 150000004760 silicates Chemical class 0.000 description 1
- 239000010802 sludge Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000011550 stock solution Substances 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 229920002994 synthetic fiber Polymers 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
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- YNJBWRMUSHSURL-UHFFFAOYSA-N trichloroacetic acid Chemical compound OC(=O)C(Cl)(Cl)Cl YNJBWRMUSHSURL-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- A01N35/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical
- A01N35/04—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having two bonds to hetero atoms with at the most one bond to halogen, e.g. aldehyde radical containing aldehyde or keto groups, or thio analogues thereof, directly attached to an aromatic ring system, e.g. acetophenone; Derivatives thereof, e.g. acetals
-
- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/10—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof
- A01N47/24—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing the groups, or; Thio analogues thereof
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (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)
- Pest Control & Pesticides (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10102279 | 2001-01-18 | ||
| DE10123734 | 2001-05-15 | ||
| PCT/EP2002/000411 WO2002056686A1 (de) | 2001-01-18 | 2002-01-17 | Fungizide mischungen |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| SK9042003A3 SK9042003A3 (en) | 2003-11-04 |
| SK287383B6 true SK287383B6 (sk) | 2010-08-09 |
Family
ID=26008280
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SK904-2003A SK287383B6 (sk) | 2001-01-18 | 2002-01-17 | Fungicídne zmesi a spôsob kontroly škodlivých plesní |
Country Status (27)
| Country | Link |
|---|---|
| US (1) | US7186672B2 (cs) |
| EP (1) | EP1353554B1 (cs) |
| JP (1) | JP2004521887A (cs) |
| KR (1) | KR100807474B1 (cs) |
| CN (1) | CN1241475C (cs) |
| AR (1) | AR035220A1 (cs) |
| AT (1) | ATE270041T1 (cs) |
| AU (1) | AU2002228050B2 (cs) |
| BG (1) | BG66185B1 (cs) |
| BR (1) | BR0206494B1 (cs) |
| CA (1) | CA2434684C (cs) |
| CZ (1) | CZ301050B6 (cs) |
| DE (1) | DE50200578D1 (cs) |
| DK (1) | DK1353554T3 (cs) |
| EA (1) | EA005609B1 (cs) |
| EE (1) | EE05227B1 (cs) |
| ES (1) | ES2224051T3 (cs) |
| HU (1) | HU230142B1 (cs) |
| IL (2) | IL156611A0 (cs) |
| MX (1) | MXPA03005758A (cs) |
| NZ (1) | NZ527419A (cs) |
| PL (1) | PL206031B1 (cs) |
| PT (1) | PT1353554E (cs) |
| SK (1) | SK287383B6 (cs) |
| TR (1) | TR200401640T4 (cs) |
| TW (1) | TWI309554B (cs) |
| WO (1) | WO2002056686A1 (cs) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN1328956C (zh) * | 2002-03-01 | 2007-08-01 | 巴斯福股份公司 | 基于Prothioconazole和嗜球果伞素衍生物的杀真菌混合物 |
| ES2282668T3 (es) * | 2002-06-20 | 2007-10-16 | Basf Aktiengesellschaft | Mezclas fungicidas a base de derivados de benzamidoxima de benzofenonas y de un azol. |
| UA80509C2 (en) * | 2004-03-30 | 2007-09-25 | Basf Ag | Fungicidal mixture, means, method for control, sowing material and use of compounds |
| DE102004049761A1 (de) * | 2004-10-12 | 2006-04-13 | Bayer Cropscience Ag | Fungizide Wirkstoffkombinationen |
| MX2009007666A (es) * | 2007-02-06 | 2009-07-27 | Basf Se | Mezclas de pesticidas. |
| EP2259675B1 (de) * | 2008-02-22 | 2015-10-07 | Basf Se | Fungizide zusammensetzungen mit 3'-brom-2,3,4,6'-tetramethoxy-2'-6-dimethylbenzophenon |
| US20120010253A1 (en) | 2009-03-16 | 2012-01-12 | Basf Se | Fungicidal compositions comprising Fluopyram and Metrafenone |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB8908794D0 (en) * | 1989-04-19 | 1989-06-07 | Janssen Pharmaceutica Nv | Synergistic compositions containing propiconazole and tebuconazole |
| KR100282840B1 (ko) | 1992-01-29 | 2001-04-02 | 스타르크, 카르크 | 카르바메이트및그를함유한작물보호제 |
| DE4423612A1 (de) | 1994-07-06 | 1996-01-11 | Basf Ag | 2-[(Dihydro)pyrazolyl-3'-oxymethylen]-anilide, Verfahren zu ihrer Herstelung und ihre Verwendung |
| CZ294096B6 (cs) | 1995-01-20 | 2004-10-13 | Americanácyanamidácompany | Benzofenonové sloučeninyŹ způsob jejich výrobyŹ fungicidní prostředky s jejich obsahem a způsob ochrany rostlin |
| BR9708873B1 (pt) * | 1996-04-26 | 2009-05-05 | mistura fungicida, e, processo para controlar fungos nocivos. | |
| EP0897904B1 (en) | 1997-08-20 | 2002-02-20 | Basf Aktiengesellschaft | Fungicidal 2-methoxybenzophenones |
| DE69812805T2 (de) | 1997-08-20 | 2003-11-13 | Basf Ag | Fungizide 2,6,6'-Trimethylbenzophenone |
| EP0967196B1 (en) | 1998-06-24 | 2003-10-22 | Basf Aktiengesellschaft | Substituted 2-hydroxybenzophenones, preparation thereof, their use as fungicide and their fungicidal compositions |
| US6346535B1 (en) | 1999-01-29 | 2002-02-12 | American Cyanamid Company | Fungicidal mixtures |
| JP2003501448A (ja) | 1999-06-14 | 2003-01-14 | シンジェンタ パーティシペーションズ アクチェンゲゼルシャフト | 併合殺菌剤 |
-
2002
- 2002-01-17 CZ CZ20031952A patent/CZ301050B6/cs not_active IP Right Cessation
- 2002-01-17 BR BRPI0206494-4B1A patent/BR0206494B1/pt not_active IP Right Cessation
- 2002-01-17 SK SK904-2003A patent/SK287383B6/sk not_active IP Right Cessation
- 2002-01-17 CA CA2434684A patent/CA2434684C/en not_active Expired - Fee Related
- 2002-01-17 EA EA200300753A patent/EA005609B1/ru not_active IP Right Cessation
- 2002-01-17 AU AU2002228050A patent/AU2002228050B2/en not_active Ceased
- 2002-01-17 JP JP2002557205A patent/JP2004521887A/ja active Pending
- 2002-01-17 PT PT02710012T patent/PT1353554E/pt unknown
- 2002-01-17 NZ NZ527419A patent/NZ527419A/xx not_active IP Right Cessation
- 2002-01-17 ES ES02710012T patent/ES2224051T3/es not_active Expired - Lifetime
- 2002-01-17 EE EEP200300337A patent/EE05227B1/xx not_active IP Right Cessation
- 2002-01-17 DE DE50200578T patent/DE50200578D1/de not_active Expired - Lifetime
- 2002-01-17 MX MXPA03005758A patent/MXPA03005758A/es active IP Right Grant
- 2002-01-17 CN CNB028037812A patent/CN1241475C/zh not_active Expired - Lifetime
- 2002-01-17 PL PL365841A patent/PL206031B1/pl unknown
- 2002-01-17 IL IL15661102A patent/IL156611A0/xx unknown
- 2002-01-17 KR KR1020037009457A patent/KR100807474B1/ko not_active Expired - Fee Related
- 2002-01-17 WO PCT/EP2002/000411 patent/WO2002056686A1/de active IP Right Grant
- 2002-01-17 EP EP02710012A patent/EP1353554B1/de not_active Expired - Lifetime
- 2002-01-17 TR TR2004/01640T patent/TR200401640T4/xx unknown
- 2002-01-17 US US10/466,168 patent/US7186672B2/en not_active Expired - Fee Related
- 2002-01-17 AT AT02710012T patent/ATE270041T1/de active
- 2002-01-17 DK DK02710012T patent/DK1353554T3/da active
- 2002-01-18 AR ARP020100184A patent/AR035220A1/es active IP Right Grant
- 2002-01-18 TW TW091100759A patent/TWI309554B/zh not_active IP Right Cessation
-
2003
- 2003-06-24 IL IL156611A patent/IL156611A/en not_active IP Right Cessation
- 2003-07-02 BG BG107964A patent/BG66185B1/bg unknown
-
2015
- 2015-07-30 HU HU0302527A patent/HU230142B1/hu not_active IP Right Cessation
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM4A | Patent lapsed due to non-payment of maintenance fees |
Effective date: 20160117 |