NL194531C - Fungicidemengsels en toepassing daarvan. - Google Patents
Fungicidemengsels en toepassing daarvan. Download PDFInfo
- Publication number
- NL194531C NL194531C NL9300989A NL9300989A NL194531C NL 194531 C NL194531 C NL 194531C NL 9300989 A NL9300989 A NL 9300989A NL 9300989 A NL9300989 A NL 9300989A NL 194531 C NL194531 C NL 194531C
- Authority
- NL
- Netherlands
- Prior art keywords
- concentration
- ppm
- anilino
- compound
- pyrimidine
- Prior art date
Links
- 230000000855 fungicidal effect Effects 0.000 title claims description 35
- 239000000203 mixture Substances 0.000 title claims description 33
- 239000000417 fungicide Substances 0.000 title description 19
- 150000001875 compounds Chemical class 0.000 claims description 28
- CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 claims description 18
- 230000000694 effects Effects 0.000 claims description 18
- 230000003631 expected effect Effects 0.000 claims description 18
- ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 claims description 10
- 241000266326 Alternaria botrytis Species 0.000 claims description 9
- 241000233866 Fungi Species 0.000 claims description 9
- 239000005785 Fluquinconazole Substances 0.000 claims description 8
- IJJVMEJXYNJXOJ-UHFFFAOYSA-N fluquinconazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1N1C(=O)C2=CC(F)=CC=C2N=C1N1C=NC=N1 IJJVMEJXYNJXOJ-UHFFFAOYSA-N 0.000 claims description 7
- 239000005741 Bromuconazole Substances 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 239000000126 substance Substances 0.000 claims description 6
- FSCWZHGZWWDELK-UHFFFAOYSA-N 3-(3,5-dichlorophenyl)-5-ethenyl-5-methyl-2,4-oxazolidinedione Chemical compound O=C1C(C)(C=C)OC(=O)N1C1=CC(Cl)=CC(Cl)=C1 FSCWZHGZWWDELK-UHFFFAOYSA-N 0.000 claims description 5
- 239000005747 Chlorothalonil Substances 0.000 claims description 5
- 239000005802 Mancozeb Substances 0.000 claims description 5
- 239000005820 Prochloraz Substances 0.000 claims description 5
- RIOXQFHNBCKOKP-UHFFFAOYSA-N benomyl Chemical compound C1=CC=C2N(C(=O)NCCCC)C(NC(=O)OC)=NC2=C1 RIOXQFHNBCKOKP-UHFFFAOYSA-N 0.000 claims description 5
- HJJVPARKXDDIQD-UHFFFAOYSA-N bromuconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCC(Br)C1 HJJVPARKXDDIQD-UHFFFAOYSA-N 0.000 claims description 5
- CRQQGFGUEAVUIL-UHFFFAOYSA-N chlorothalonil Chemical compound ClC1=C(Cl)C(C#N)=C(Cl)C(C#N)=C1Cl CRQQGFGUEAVUIL-UHFFFAOYSA-N 0.000 claims description 5
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 claims description 5
- MGNFYQILYYYUBS-UHFFFAOYSA-N 1-[3-(4-tert-butylphenyl)-2-methylpropyl]piperidine Chemical compound C=1C=C(C(C)(C)C)C=CC=1CC(C)CN1CCCCC1 MGNFYQILYYYUBS-UHFFFAOYSA-N 0.000 claims description 4
- 239000005777 Fenpropidin Substances 0.000 claims description 4
- 239000005842 Thiophanate-methyl Substances 0.000 claims description 4
- 239000005843 Thiram Substances 0.000 claims description 4
- MITFXPHMIHQXPI-UHFFFAOYSA-N benzoxaprofen Natural products N=1C2=CC(C(C(O)=O)C)=CC=C2OC=1C1=CC=C(Cl)C=C1 MITFXPHMIHQXPI-UHFFFAOYSA-N 0.000 claims description 4
- FBOUIAKEJMZPQG-BLXFFLACSA-N diniconazole-M Chemical compound C1=NC=NN1/C([C@H](O)C(C)(C)C)=C/C1=CC=C(Cl)C=C1Cl FBOUIAKEJMZPQG-BLXFFLACSA-N 0.000 claims description 4
- -1 iprodion Chemical compound 0.000 claims description 4
- 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 claims description 4
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims description 4
- 229960002447 thiram Drugs 0.000 claims description 4
- KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 0.000 claims description 3
- 230000003032 phytopathogenic effect Effects 0.000 claims description 3
- WFDXOXNFNRHQEC-GHRIWEEISA-N azoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C#N)=NC=N1 WFDXOXNFNRHQEC-GHRIWEEISA-N 0.000 claims description 2
- 235000013339 cereals Nutrition 0.000 description 7
- 239000013543 active substance Substances 0.000 description 6
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 6
- OWDLFBLNMPCXSD-UHFFFAOYSA-N 2-chloro-N-(2,6-dimethylphenyl)-N-(2-oxotetrahydrofuran-3-yl)acetamide Chemical compound CC1=CC=CC(C)=C1N(C(=O)CCl)C1C(=O)OCC1 OWDLFBLNMPCXSD-UHFFFAOYSA-N 0.000 description 5
- 235000007319 Avena orientalis Nutrition 0.000 description 4
- 244000075850 Avena orientalis Species 0.000 description 4
- 241000196324 Embryophyta Species 0.000 description 4
- 150000008059 anilinopyrimidines Chemical class 0.000 description 4
- 239000003085 diluting agent Substances 0.000 description 4
- 238000005507 spraying Methods 0.000 description 4
- 229920001817 Agar Polymers 0.000 description 3
- 240000005979 Hordeum vulgare Species 0.000 description 3
- 235000007340 Hordeum vulgare Nutrition 0.000 description 3
- 239000005867 Iprodione Substances 0.000 description 3
- 241001330975 Magnaporthe oryzae Species 0.000 description 3
- 244000141359 Malus pumila Species 0.000 description 3
- 241001459558 Monographella nivalis Species 0.000 description 3
- 239000008272 agar Substances 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 201000010099 disease Diseases 0.000 description 3
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000575 pesticide Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000243 solution Substances 0.000 description 3
- 230000002195 synergetic effect Effects 0.000 description 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
- 235000011430 Malus pumila Nutrition 0.000 description 2
- 235000015103 Malus silvestris Nutrition 0.000 description 2
- 240000007594 Oryza sativa Species 0.000 description 2
- 235000007164 Oryza sativa Nutrition 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- 241000221696 Sclerotinia sclerotiorum Species 0.000 description 2
- 235000021307 Triticum Nutrition 0.000 description 2
- 241000209140 Triticum Species 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 239000002270 dispersing agent Substances 0.000 description 2
- 239000004495 emulsifiable concentrate Substances 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 238000009472 formulation Methods 0.000 description 2
- ONUFESLQCSAYKA-UHFFFAOYSA-N iprodione Chemical compound O=C1N(C(=O)NC(C)C)CC(=O)N1C1=CC(Cl)=CC(Cl)=C1 ONUFESLQCSAYKA-UHFFFAOYSA-N 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 235000009566 rice Nutrition 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 150000003431 steroids Chemical class 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- PXMNMQRDXWABCY-UHFFFAOYSA-N 1-(4-chlorophenyl)-4,4-dimethyl-3-(1H-1,2,4-triazol-1-ylmethyl)pentan-3-ol Chemical compound C1=NC=NN1CC(O)(C(C)(C)C)CCC1=CC=C(Cl)C=C1 PXMNMQRDXWABCY-UHFFFAOYSA-N 0.000 description 1
- 125000004201 2,4-dichlorophenyl group Chemical group [H]C1=C([H])C(*)=C(Cl)C([H])=C1Cl 0.000 description 1
- HNVIQLPOGUDBSU-UHFFFAOYSA-N 2,6-dimethylmorpholine Chemical compound CC1CNCC(C)O1 HNVIQLPOGUDBSU-UHFFFAOYSA-N 0.000 description 1
- UFNOUKDBUJZYDE-UHFFFAOYSA-N 2-(4-chlorophenyl)-3-cyclopropyl-1-(1H-1,2,4-triazol-1-yl)butan-2-ol Chemical compound C1=NC=NN1CC(O)(C=1C=CC(Cl)=CC=1)C(C)C1CC1 UFNOUKDBUJZYDE-UHFFFAOYSA-N 0.000 description 1
- IQHSSYROJYPFDV-UHFFFAOYSA-N 2-bromo-1,3-dichloro-5-(trifluoromethyl)benzene Chemical group FC(F)(F)C1=CC(Cl)=C(Br)C(Cl)=C1 IQHSSYROJYPFDV-UHFFFAOYSA-N 0.000 description 1
- NSPMIYGKQJPBQR-UHFFFAOYSA-N 4H-1,2,4-triazole Chemical compound C=1N=CNN=1 NSPMIYGKQJPBQR-UHFFFAOYSA-N 0.000 description 1
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 1
- 239000005995 Aluminium silicate Substances 0.000 description 1
- 241000228212 Aspergillus Species 0.000 description 1
- 241000981372 Aspergillus sclerotiorum Species 0.000 description 1
- 241000219310 Beta vulgaris subsp. vulgaris Species 0.000 description 1
- 241001480061 Blumeria graminis Species 0.000 description 1
- 241001465180 Botrytis Species 0.000 description 1
- 241000123650 Botrytis cinerea Species 0.000 description 1
- 241001157813 Cercospora Species 0.000 description 1
- 235000008733 Citrus aurantifolia Nutrition 0.000 description 1
- 235000005979 Citrus limon Nutrition 0.000 description 1
- 244000131522 Citrus pyriformis Species 0.000 description 1
- 241000371644 Curvularia ravenelii Species 0.000 description 1
- 239000005757 Cyproconazole Substances 0.000 description 1
- 241001149475 Gaeumannomyces graminis Species 0.000 description 1
- PWHULOQIROXLJO-UHFFFAOYSA-N Manganese Chemical compound [Mn] PWHULOQIROXLJO-UHFFFAOYSA-N 0.000 description 1
- 241001668536 Oculimacula yallundae Species 0.000 description 1
- 241000736122 Parastagonospora nodorum Species 0.000 description 1
- 241000228143 Penicillium Species 0.000 description 1
- 206010035148 Plague Diseases 0.000 description 1
- 241000896203 Podosphaera pannosa Species 0.000 description 1
- 239000005822 Propiconazole Substances 0.000 description 1
- 241000221301 Puccinia graminis Species 0.000 description 1
- 241000228453 Pyrenophora Species 0.000 description 1
- 241000520647 Pyrenophora avenae Species 0.000 description 1
- 239000005828 Pyrimethanil Substances 0.000 description 1
- 241000220324 Pyrus Species 0.000 description 1
- 241001515790 Rhynchosporium secalis Species 0.000 description 1
- 235000004789 Rosa xanthina Nutrition 0.000 description 1
- 241000109329 Rosa xanthina Species 0.000 description 1
- 206010039509 Scab Diseases 0.000 description 1
- 241001518640 Sclerotinia homoeocarpa Species 0.000 description 1
- 235000007238 Secale cereale Nutrition 0.000 description 1
- 244000082988 Secale cereale Species 0.000 description 1
- 244000061456 Solanum tuberosum Species 0.000 description 1
- 235000002595 Solanum tuberosum Nutrition 0.000 description 1
- 235000021536 Sugar beet Nutrition 0.000 description 1
- 239000005839 Tebuconazole Substances 0.000 description 1
- 235000011941 Tilia x europaea Nutrition 0.000 description 1
- 241000722093 Tilletia caries Species 0.000 description 1
- 241000509513 Ustilago hordei Species 0.000 description 1
- 241000007070 Ustilago nuda Species 0.000 description 1
- 241000228452 Venturia inaequalis Species 0.000 description 1
- 241000607479 Yersinia pestis Species 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 229940051881 anilide analgesics and antipyretics Drugs 0.000 description 1
- 150000003931 anilides Chemical class 0.000 description 1
- 230000003042 antagnostic effect Effects 0.000 description 1
- 235000021016 apples Nutrition 0.000 description 1
- 239000013011 aqueous formulation Substances 0.000 description 1
- 229960000892 attapulgite Drugs 0.000 description 1
- DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 150000004699 copper complex Chemical class 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 230000017858 demethylation Effects 0.000 description 1
- 238000010520 demethylation reaction Methods 0.000 description 1
- 235000021186 dishes Nutrition 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 239000012990 dithiocarbamate Substances 0.000 description 1
- 238000010410 dusting Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 230000009969 flowable effect Effects 0.000 description 1
- FQKUGOMFVDPBIZ-UHFFFAOYSA-N flusilazole Chemical compound C=1C=C(F)C=CC=1[Si](C=1C=CC(F)=CC=1)(C)CN1C=NC=N1 FQKUGOMFVDPBIZ-UHFFFAOYSA-N 0.000 description 1
- 238000000227 grinding Methods 0.000 description 1
- 230000009036 growth inhibition Effects 0.000 description 1
- 230000002363 herbicidal effect Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000010903 husk Substances 0.000 description 1
- 238000000338 in vitro Methods 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000003112 inhibitor Substances 0.000 description 1
- 230000003993 interaction Effects 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
- 239000004571 lime Substances 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 239000011572 manganese Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 230000017066 negative regulation of growth Effects 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 229910052625 palygorskite Inorganic materials 0.000 description 1
- 235000021017 pears Nutrition 0.000 description 1
- YLVKIBKAGUPACT-UHFFFAOYSA-N phenylazaniumylideneazanide Chemical group [N]NC1=CC=CC=C1 YLVKIBKAGUPACT-UHFFFAOYSA-N 0.000 description 1
- 235000012015 potatoes Nutrition 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000003449 preventive effect Effects 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
- 239000002689 soil Substances 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 239000004563 wettable powder Substances 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
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)
Applications Claiming Priority (6)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9212332 | 1992-06-10 | ||
| GB929212332A GB9212332D0 (en) | 1992-06-10 | 1992-06-10 | Fungicidal compositions |
| GB929212877A GB9212877D0 (en) | 1992-06-17 | 1992-06-17 | Fungicidal compositions |
| GB9212877 | 1992-06-17 | ||
| GB929222839A GB9222839D0 (en) | 1992-10-30 | 1992-10-30 | Fundicidal compositions |
| GB9222839 | 1992-10-30 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NL9300989A NL9300989A (nl) | 1994-01-03 |
| NL194531B NL194531B (nl) | 2002-03-01 |
| NL194531C true NL194531C (nl) | 2002-07-02 |
Family
ID=27266239
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL9300989A NL194531C (nl) | 1992-06-10 | 1993-06-09 | Fungicidemengsels en toepassing daarvan. |
Country Status (11)
| Country | Link |
|---|---|
| JP (1) | JP3643386B2 (pl) |
| AT (1) | AT402878B (pl) |
| AU (1) | AU659016B2 (pl) |
| BE (1) | BE1006697A5 (pl) |
| DE (1) | DE4318372B4 (pl) |
| FR (1) | FR2692108B1 (pl) |
| HU (1) | HU212898B (pl) |
| IL (1) | IL105941A (pl) |
| IT (1) | IT1268412B1 (pl) |
| NL (1) | NL194531C (pl) |
| PL (1) | PL172180B1 (pl) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| TW286264B (pl) * | 1994-05-20 | 1996-09-21 | Ciba Geigy Ag | |
| FR2828065B1 (fr) * | 2001-08-01 | 2004-07-16 | Aventis Cropscience Sa | Composition fongicide et utilisation de cette composition pour la lutte contre les maladies des plantes |
| FR2829669A1 (fr) * | 2001-09-18 | 2003-03-21 | Aventis Cropscience Sa | Composition fongicide comprenant un compose de la famille des anilinopyrimidines et de l'iprodione |
| ITMI20012430A1 (it) * | 2001-11-19 | 2003-05-19 | Isagro Spa | Composizioni a base di sali rameici sali rameici e loro utilizzo per il controllo di fitopatogeni |
| AU2003246635A1 (en) * | 2002-07-10 | 2004-02-02 | Basf Aktiengesellschaft | Fungicidal mixtures based on dithianon |
| EP1413198A1 (fr) * | 2002-10-24 | 2004-04-28 | Bayer CropScience SA | Utilisation du pyrimethanil sur des pathogènes résistants |
| CA2554236C (en) * | 2004-02-04 | 2012-09-11 | Janssen Pharmaceutica N.V. | Synergistic antifungal didecyl dimethyl ammonium chloride compositions |
| EP1570737A1 (en) * | 2004-02-12 | 2005-09-07 | Bayer CropScience S.A. | Fungicidal composition comprising a pyridylethylbenzamide derivative and a compound capable of inhibiting the methionine biosynthesis |
| GB0525567D0 (en) * | 2005-12-15 | 2006-01-25 | Syngenta Participations Ag | Novel materials and methods for the production thereof |
| ES2364315T3 (es) * | 2007-08-09 | 2011-08-31 | Basf Se | Mezclas fungicidas. |
| EP2200438B1 (en) * | 2007-09-07 | 2011-07-13 | Janssen Pharmaceutica NV | Combinations of pyrimethanil and silver compounds |
| AR071344A1 (es) * | 2008-02-05 | 2010-06-16 | Basf Se | Mezclas de plaguicidas |
| EP2253206B1 (en) * | 2008-03-21 | 2014-01-01 | Sumitomo Chemical Company, Limited | Plant disease control composition |
| JP2015214510A (ja) * | 2014-05-09 | 2015-12-03 | 株式会社クレハ | 農園芸用薬剤、植物病害防除方法および植物病害防除用製品 |
| CN104351186B (zh) * | 2014-11-11 | 2016-08-17 | 青岛青知企业管理咨询有限公司 | 有效成分为大蒜素和嘧霉胺的复合杀菌剂 |
| EP3808179A1 (en) * | 2019-10-16 | 2021-04-21 | LANXESS Deutschland GmbH | Fungicide mixtures |
| EP3808178B1 (en) * | 2019-10-16 | 2024-12-11 | LANXESS Deutschland GmbH | Fungicide mixtures |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DD151404A1 (de) * | 1980-06-13 | 1981-10-21 | Friedrich Franke | Fungizide mittel |
| DE3614060A1 (de) * | 1986-04-23 | 1987-10-29 | Schering Ag | Pyrimidin-derivate, verfahren zu ihrer herstellung und ihre verwendung als fungizide |
| JPH0784445B2 (ja) * | 1986-12-03 | 1995-09-13 | クミアイ化学工業株式会社 | ピリミジン誘導体および農園芸用殺菌剤 |
| EP0310550B1 (de) * | 1987-09-28 | 1993-05-26 | Ciba-Geigy Ag | Schädlingsbekämpfungsmittel |
| GB9020207D0 (en) * | 1990-09-15 | 1990-10-24 | Schering Ag | Fungicides |
| US5522203A (en) * | 1990-10-02 | 1996-06-04 | Lantech, Inc. | Biaxial stretch wrapping |
| JP3086741B2 (ja) * | 1991-02-07 | 2000-09-11 | クミアイ化学工業株式会社 | 農園芸用殺菌剤組成物 |
| JP3086746B2 (ja) * | 1991-03-20 | 2000-09-11 | クミアイ化学工業株式会社 | 農園芸用殺菌剤組成物 |
| JPH0578211A (ja) * | 1991-09-18 | 1993-03-30 | Kaiyo Kagaku Kk | 水中生物防汚剤 |
| EP0556157B1 (de) * | 1992-02-13 | 1997-11-26 | Novartis AG | Fungizide Mischungen auf der Basis von Triazol-Fungiziden und 4,6-Dimethyl-N-Phenyl-2-Pyrimidinamin |
-
1993
- 1993-05-28 DE DE4318372A patent/DE4318372B4/de not_active Expired - Lifetime
- 1993-06-07 BE BE9300573A patent/BE1006697A5/fr not_active IP Right Cessation
- 1993-06-08 AU AU40099/93A patent/AU659016B2/en not_active Expired
- 1993-06-08 FR FR9306849A patent/FR2692108B1/fr not_active Expired - Lifetime
- 1993-06-08 IL IL105941A patent/IL105941A/xx not_active IP Right Cessation
- 1993-06-09 HU HU9301686A patent/HU212898B/hu unknown
- 1993-06-09 PL PL93299259A patent/PL172180B1/pl unknown
- 1993-06-09 NL NL9300989A patent/NL194531C/nl not_active IP Right Cessation
- 1993-06-09 AT AT0112693A patent/AT402878B/de not_active IP Right Cessation
- 1993-06-10 IT IT93MI001233A patent/IT1268412B1/it active IP Right Grant
- 1993-06-10 JP JP13838593A patent/JP3643386B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE4318372B4 (de) | 2010-10-28 |
| HU9301686D0 (en) | 1993-09-28 |
| PL172180B1 (pl) | 1997-08-29 |
| BE1006697A5 (fr) | 1994-11-22 |
| FR2692108B1 (fr) | 1995-01-27 |
| NL194531B (nl) | 2002-03-01 |
| ITMI931233A0 (it) | 1993-06-10 |
| DE4318372A1 (de) | 1993-12-16 |
| ATA112693A (de) | 1997-02-15 |
| FR2692108A1 (fr) | 1993-12-17 |
| IT1268412B1 (it) | 1997-02-27 |
| PL299259A1 (en) | 1994-02-21 |
| IL105941A0 (en) | 1993-10-20 |
| AU659016B2 (en) | 1995-05-04 |
| AT402878B (de) | 1997-09-25 |
| JP3643386B2 (ja) | 2005-04-27 |
| IL105941A (en) | 1997-07-13 |
| NL9300989A (nl) | 1994-01-03 |
| JPH0656610A (ja) | 1994-03-01 |
| HUT64178A (en) | 1993-12-28 |
| AU4009993A (en) | 1993-12-23 |
| HU212898B (en) | 1996-12-30 |
| ITMI931233A1 (it) | 1994-12-10 |
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