DE10141617A1 - Fungizide Wirkstoffkombinationen - Google Patents

Fungizide Wirkstoffkombinationen

Info

Publication number: DE10141617A1
Authority: DE; Germany
Prior art keywords: active ingredient; formula; group; parts; active
Prior art date: 2001-08-24
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.): Withdrawn

Application number

DE2001141617

Other languages

German (de)

English (en)

Inventor

Ulrike Wachendorff-Neumann

Thomas Seitz

Ulrich Heinemann

Herbert Gayer

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Bayer CropScience AG

Original Assignee

Bayer CropScience AG

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2001-08-24

Filing date

2001-08-24

Publication date

2003-03-06

2001-08-24 Application filed by Bayer CropScience AG filed Critical Bayer CropScience AG

2001-08-24 Priority to DE2001141617 priority Critical patent/DE10141617A1/de

2002-08-12 Priority to AU2002325940A priority patent/AU2002325940A1/en

2002-08-12 Priority to PCT/EP2002/008999 priority patent/WO2003017762A2/fr

2003-03-06 Publication of DE10141617A1 publication Critical patent/DE10141617A1/de

Status Withdrawn legal-status Critical Current

Links

239000004480 active ingredient Substances 0.000 title claims abstract description 94
230000000855 fungicidal effect Effects 0.000 title claims abstract description 12
241000233866 Fungi Species 0.000 claims abstract description 6
150000001875 compounds Chemical class 0.000 claims description 29
239000000203 mixture Substances 0.000 claims description 16
-1 Cu 2 Cl (OH) 3 Chemical class 0.000 claims description 14
239000013543 active substance Substances 0.000 claims description 12
HKMOPYJWSFRURD-UHFFFAOYSA-N chloro hypochlorite;copper Chemical class [Cu].ClOCl HKMOPYJWSFRURD-UHFFFAOYSA-N 0.000 claims description 6
238000000034 method Methods 0.000 claims description 6
239000000460 chlorine Substances 0.000 claims description 5
HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 0.000 claims description 5
HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 claims description 5
239000004606 Fillers/Extenders Substances 0.000 claims description 4
239000005789 Folpet Substances 0.000 claims description 4
239000005802 Mancozeb Substances 0.000 claims description 4
239000005823 Propineb Substances 0.000 claims description 4
KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 4
239000010949 copper Substances 0.000 claims description 4
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 4
KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 claims description 4
XERJKGMBORTKEO-VZUCSPMQSA-N (1e)-2-(ethylcarbamoylamino)-n-methoxy-2-oxoethanimidoyl cyanide Chemical compound CCNC(=O)NC(=O)C(\C#N)=N\OC XERJKGMBORTKEO-VZUCSPMQSA-N 0.000 claims description 3
LDVVMCZRFWMZSG-OLQVQODUSA-N (3ar,7as)-2-(trichloromethylsulfanyl)-3a,4,7,7a-tetrahydroisoindole-1,3-dione Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)Cl)C(=O)[C@H]21 LDVVMCZRFWMZSG-OLQVQODUSA-N 0.000 claims description 3
125000001622 2-naphthyl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C(*)C([H])=C([H])C2=C1[H] 0.000 claims description 3
125000000590 4-methylphenyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 claims description 3
235000001674 Agaricus brunnescens Nutrition 0.000 claims description 3
239000005745 Captan Substances 0.000 claims description 3
239000005747 Chlorothalonil Substances 0.000 claims description 3
239000005756 Cymoxanil Substances 0.000 claims description 3
239000005764 Dithianon Substances 0.000 claims description 3
239000005780 Fluazinam Substances 0.000 claims description 3
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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 3
WURGXGVFSMYFCG-UHFFFAOYSA-N dichlofluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=CC=C1 WURGXGVFSMYFCG-UHFFFAOYSA-N 0.000 claims description 3
PYZSVQVRHDXQSL-UHFFFAOYSA-N dithianon Chemical compound S1C(C#N)=C(C#N)SC2=C1C(=O)C1=CC=CC=C1C2=O PYZSVQVRHDXQSL-UHFFFAOYSA-N 0.000 claims description 3
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 3
UZCGKGPEKUCDTF-UHFFFAOYSA-N fluazinam Chemical compound [O-][N+](=O)C1=CC(C(F)(F)F)=C(Cl)C([N+]([O-])=O)=C1NC1=NC=C(C(F)(F)F)C=C1Cl UZCGKGPEKUCDTF-UHFFFAOYSA-N 0.000 claims description 3
VUERQRKTYBIULR-UHFFFAOYSA-N fosetyl Chemical compound CCOP(O)=O VUERQRKTYBIULR-UHFFFAOYSA-N 0.000 claims description 3
125000003392 indanyl group Chemical group C1(CCC2=CC=CC=C12)* 0.000 claims description 3
ZQEIXNIJLIKNTD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-(methoxyacetyl)alaninate Chemical compound COCC(=O)N(C(C)C(=O)OC)C1=C(C)C=CC=C1C ZQEIXNIJLIKNTD-UHFFFAOYSA-N 0.000 claims description 3
CIEXPHRYOLIQQD-UHFFFAOYSA-N methyl N-(2,6-dimethylphenyl)-N-2-furoylalaninate Chemical compound CC=1C=CC=C(C)C=1N(C(C)C(=O)OC)C(=O)C1=CC=CO1 CIEXPHRYOLIQQD-UHFFFAOYSA-N 0.000 claims description 3
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125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
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229960002447 thiram Drugs 0.000 claims description 3
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims description 3
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WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims description 2
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229910052782 aluminium Inorganic materials 0.000 claims description 2
XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims description 2
229910052794 bromium Inorganic materials 0.000 claims description 2
229910052801 chlorine Inorganic materials 0.000 claims description 2
239000011737 fluorine Substances 0.000 claims description 2
229910052731 fluorine Inorganic materials 0.000 claims description 2
125000001153 fluoro group Chemical group F* 0.000 claims description 2
BSDQITJYKQHXQR-UHFFFAOYSA-N methyl prop-2-eneperoxoate Chemical compound COOC(=O)C=C BSDQITJYKQHXQR-UHFFFAOYSA-N 0.000 claims description 2
QAZLUNIWYYOJPC-UHFFFAOYSA-M sulfenamide Chemical compound [Cl-].COC1=C(C)C=[N+]2C3=NC4=CC=C(OC)C=C4N3SCC2=C1C QAZLUNIWYYOJPC-UHFFFAOYSA-M 0.000 claims description 2
XDEHMKQLKPZERH-BYPYZUCNSA-N (2s)-2-amino-3-methylbutanamide Chemical class CC(C)[C@H](N)C(N)=O XDEHMKQLKPZERH-BYPYZUCNSA-N 0.000 abstract description 5
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244000061456 Solanum tuberosum Species 0.000 description 5
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RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
239000000969 carrier Substances 0.000 description 4
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GUJOJGAPFQRJSV-UHFFFAOYSA-N dialuminum;dioxosilane;oxygen(2-);hydrate Chemical compound O.[O-2].[O-2].[O-2].[Al+3].[Al+3].O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O GUJOJGAPFQRJSV-UHFFFAOYSA-N 0.000 description 1
235000014113 dietary fatty acids Nutrition 0.000 description 1
201000010099 disease Diseases 0.000 description 1
208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 1
230000009189 diving Effects 0.000 description 1
239000010459 dolomite Substances 0.000 description 1
229910000514 dolomite Inorganic materials 0.000 description 1
239000000890 drug combination Substances 0.000 description 1
239000005712 elicitor Substances 0.000 description 1
239000004495 emulsifiable concentrate Substances 0.000 description 1
238000005538 encapsulation Methods 0.000 description 1
150000002148 esters Chemical class 0.000 description 1
150000002170 ethers Chemical class 0.000 description 1
KQTVWCSONPJJPE-UHFFFAOYSA-N etridiazole Chemical compound CCOC1=NC(C(Cl)(Cl)Cl)=NS1 KQTVWCSONPJJPE-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
239000000194 fatty acid Substances 0.000 description 1
229930195729 fatty acid Natural products 0.000 description 1
150000002191 fatty alcohols Chemical class 0.000 description 1
239000003337 fertilizer Substances 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000004088 foaming agent Substances 0.000 description 1
230000004927 fusion Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
238000012239 gene modification Methods 0.000 description 1
230000005017 genetic modification Effects 0.000 description 1
235000013617 genetically modified food Nutrition 0.000 description 1
235000021021 grapes Nutrition 0.000 description 1
230000012010 growth Effects 0.000 description 1
239000003630 growth substance Substances 0.000 description 1
125000000623 heterocyclic group Chemical group 0.000 description 1
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
208000015181 infectious disease Diseases 0.000 description 1
229910052500 inorganic mineral Inorganic materials 0.000 description 1
239000001023 inorganic pigment Substances 0.000 description 1
239000002917 insecticide Substances 0.000 description 1
229910052742 iron Inorganic materials 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
239000000787 lecithin Substances 0.000 description 1
235000010445 lecithin Nutrition 0.000 description 1
231100001231 less toxic Toxicity 0.000 description 1
229920005610 lignin Polymers 0.000 description 1
WPBNNNQJVZRUHP-UHFFFAOYSA-L manganese(2+);methyl n-[[2-(methoxycarbonylcarbamothioylamino)phenyl]carbamothioyl]carbamate;n-[2-(sulfidocarbothioylamino)ethyl]carbamodithioate Chemical class [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
239000004579 marble Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
229920000609 methyl cellulose Polymers 0.000 description 1
239000001923 methylcellulose Substances 0.000 description 1
235000010981 methylcellulose Nutrition 0.000 description 1
230000000813 microbial effect Effects 0.000 description 1
239000002480 mineral oil Substances 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
150000002780 morpholines Chemical class 0.000 description 1
238000002703 mutagenesis Methods 0.000 description 1
231100000350 mutagenesis Toxicity 0.000 description 1
IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
229940042880 natural phospholipid Drugs 0.000 description 1
239000005645 nematicide Substances 0.000 description 1
JCXJVPUVTGWSNB-UHFFFAOYSA-N nitrogen dioxide Inorganic materials O=[N]=O JCXJVPUVTGWSNB-UHFFFAOYSA-N 0.000 description 1
235000015097 nutrients Nutrition 0.000 description 1
230000035764 nutrition Effects 0.000 description 1
238000005457 optimization Methods 0.000 description 1
210000000056 organ Anatomy 0.000 description 1
239000011368 organic material Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 1
229910052625 palygorskite Inorganic materials 0.000 description 1
239000006072 paste Substances 0.000 description 1
235000021017 pears Nutrition 0.000 description 1
239000003208 petroleum Substances 0.000 description 1
150000003904 phospholipids Chemical class 0.000 description 1
239000001007 phthalocyanine dye Substances 0.000 description 1
239000000280 phytoalexin Substances 0.000 description 1
150000001857 phytoalexin derivatives Chemical class 0.000 description 1
239000002798 polar solvent Substances 0.000 description 1
229920000151 polyglycol Polymers 0.000 description 1
239000010695 polyglycol Substances 0.000 description 1
229920000642 polymer Polymers 0.000 description 1
239000011118 polyvinyl acetate Substances 0.000 description 1
229920002689 polyvinyl acetate Polymers 0.000 description 1
229920002451 polyvinyl alcohol Polymers 0.000 description 1
239000001294 propane Substances 0.000 description 1
239000003380 propellant Substances 0.000 description 1
239000003531 protein hydrolysate Substances 0.000 description 1
210000001938 protoplast Anatomy 0.000 description 1
239000008262 pumice Substances 0.000 description 1
239000010453 quartz Substances 0.000 description 1
230000004044 response Effects 0.000 description 1
235000009566 rice Nutrition 0.000 description 1
229910052624 sepiolite Inorganic materials 0.000 description 1
235000019355 sepiolite Nutrition 0.000 description 1
150000004760 silicates Chemical class 0.000 description 1
239000000377 silicon dioxide Substances 0.000 description 1
239000002002 slurry Substances 0.000 description 1
238000003860 storage Methods 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
HOWHQWFXSLOJEF-MGZLOUMQSA-N systemin Chemical compound NCCCC[C@H](N)C(=O)N[C@@H](CCSC)C(=O)N[C@@H](CCC(N)=O)C(=O)N[C@@H]([C@@H](C)O)C(=O)N[C@@H](CC(O)=O)C(=O)OC(=O)[C@@H]1CCCN1C(=O)[C@H]1N(C(=O)[C@H](CC(O)=O)NC(=O)[C@H](CCCN=C(N)N)NC(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H]2N(CCC2)C(=O)[C@H]2N(CCC2)C(=O)[C@H](CCCCN)NC(=O)[C@H](CO)NC(=O)[C@H](CCC(N)=O)NC(=O)[C@@H](NC(=O)[C@H](C)N)C(C)C)CCC1 HOWHQWFXSLOJEF-MGZLOUMQSA-N 0.000 description 1
108010050014 systemin Proteins 0.000 description 1
239000000454 talc Substances 0.000 description 1
229910052623 talc Inorganic materials 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
229960004295 valine Drugs 0.000 description 1
235000015112 vegetable and seed oil Nutrition 0.000 description 1
239000008158 vegetable oil Substances 0.000 description 1
239000008096 xylene Substances 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
- 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
- A01N47/12—Carbamic acid derivatives, i.e. containing the group —O—CO—N<; Thio analogues thereof containing a —O—CO—N< group, or a thio analogue thereof, neither directly attached to a ring nor the nitrogen atom being a member of a heterocyclic ring

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)
Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

DE2001141617 2001-08-24 2001-08-24 Fungizide Wirkstoffkombinationen Withdrawn DE10141617A1 (de)

Priority Applications (3)

Application Number	Priority Date	Filing Date	Title
DE2001141617 DE10141617A1 (de)	2001-08-24	2001-08-24	Fungizide Wirkstoffkombinationen
AU2002325940A AU2002325940A1 (en)	2001-08-24	2002-08-12	Fungicidal active-ingredient combinations
PCT/EP2002/008999 WO2003017762A2 (fr)	2001-08-24	2002-08-12	Combinaisons de substances actives fongicides

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE2001141617 DE10141617A1 (de)	2001-08-24	2001-08-24	Fungizide Wirkstoffkombinationen

Publications (1)

Publication Number	Publication Date
DE10141617A1 true DE10141617A1 (de)	2003-03-06

Family

ID=7696545

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
DE2001141617 Withdrawn DE10141617A1 (de)	2001-08-24	2001-08-24	Fungizide Wirkstoffkombinationen

Country Status (3)

Country	Link
AU (1)	AU2002325940A1 (fr)
DE (1)	DE10141617A1 (fr)
WO (1)	WO2003017762A2 (fr)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
GB0227966D0 (en) *	2002-11-29	2003-01-08	Syngenta Participations Ag	Organic Compounds
WO2005077187A1 (fr) *	2004-02-18	2005-08-25	Tecnotrea S.R.L.	Melanges fongicides synergiques
EP1830653A1 (fr) *	2004-12-23	2007-09-12	Basf Aktiengesellschaft	Melanges fongicides
DE102005026482A1 (de) *	2005-06-09	2006-12-14	Bayer Cropscience Ag	Wirkstoffkombinationen
ATE484194T1 (de)	2005-06-09	2010-10-15	Bayer Cropscience Ag	Wirkstoffkombinationen
CN101647466B (zh) *	2009-07-15	2013-04-10	深圳诺普信农化股份有限公司	杀菌组合物
EP2292094A1 (fr) *	2009-09-02	2011-03-09	Bayer CropScience AG	Combinaisons de composés actifs
KR20170009896A (ko) *	2014-05-15	2017-01-25	바이엘 크롭사이언스 악티엔게젤샤프트	활성 화합물의 배합물

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4026966A1 (de) *	1990-08-25	1992-02-27	Bayer Ag	Substituierte valinamid-derivate
DE4304172A1 (de) *	1993-02-12	1994-08-25	Bayer Ag	Fungizide Wirkstoffkombinationen
GB9819317D0 (en) *	1998-09-04	1998-10-28	Novartis Ag	Organic compounds

2001
- 2001-08-24 DE DE2001141617 patent/DE10141617A1/de not_active Withdrawn
2002
- 2002-08-12 WO PCT/EP2002/008999 patent/WO2003017762A2/fr not_active Ceased
- 2002-08-12 AU AU2002325940A patent/AU2002325940A1/en not_active Abandoned

Also Published As

Publication number	Publication date
WO2003017762A2 (fr)	2003-03-06
WO2003017762A3 (fr)	2004-05-27
AU2002325940A1 (en)	2003-03-10

Publication	Publication Date	Title
EP2319308B1 (fr)	2017-06-07	Composition fongicide comprennant fluoxastrobin et un autre agent fongicide
EP1517609B1 (fr)	2008-01-16	Combinaisons de substances actives fongicides
EP1677598B1 (fr)	2014-11-26	Combinaisons d'agents actifs synergiques fongicides
EP2220935B1 (fr)	2012-11-28	Combinaisons de fongicides synergétiques
EP1651040B1 (fr)	2009-05-27	Combinaisons fongicides ternaires de principes actifs
EP1463410B1 (fr)	2009-04-15	Combinaisons de substances actives fongicides
DE10228102A1 (de)	2004-01-15	Fungizide Wirkstoffkombinationen
DE10228104A1 (de)	2004-01-15	Fungizide Wirkstoffkombination
EP1276375B1 (fr)	2005-07-20	Combinaisons de principes actifs fongicides
WO2001084931A1 (fr)	2001-11-15	Combinaisons de principes actifs fongicides
EP1677600B1 (fr)	2009-06-24	Associations de principes actifs fongicides contenant de la spiroxamine, du prothioconazole et du tebuconazole
DE102005015850A1 (de)	2006-10-12	Synergistische fungizide Wirkstoffkombinationen
DE10141617A1 (de)	2003-03-06	Fungizide Wirkstoffkombinationen
DE102004017981A1 (de)	2005-11-03	Fungizide Wirkstoffkombinationen
DE10352264A1 (de)	2005-06-09	Fungizide Wirkstoffkombination
DE102004027430A1 (de)	2005-12-29	Fungizide Wirkstoffkombination
EP2027773A1 (fr)	2009-02-25	Utilisation de N-[2-(1,3-diméthylbutyl)phényl]-5-fluor-1,3-diméthyl-1H-pyrazole-4-carboxamide
DE102004027431A1 (de)	2005-12-29	Fungizide Wirkstoffkombination

Legal Events

Date	Code	Title	Description
2004-06-09	8139	Disposal/non-payment of the annual fee