BE1006697A5 - Melanges fongicides. - Google Patents

Melanges fongicides. Download PDF

Info

Publication number: BE1006697A5
Authority: BE; Belgium
Prior art keywords: sep; compound; composition according; methyl; triazol
Prior art date: 1992-06-10

Application number

BE9300573A

Other languages

English (en)

French (fr)

Original Assignee

Schering 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.)

1992-06-10

Filing date

1993-06-07

Publication date

1994-11-22

1992-06-10 Priority claimed from GB929212332A external-priority patent/GB9212332D0/en

1992-06-17 Priority claimed from GB929212877A external-priority patent/GB9212877D0/en

1992-10-30 Priority claimed from GB929222839A external-priority patent/GB9222839D0/en

1993-06-07 Application filed by Schering Ag filed Critical Schering Ag

1994-11-22 Application granted granted Critical

1994-11-22 Publication of BE1006697A5 publication Critical patent/BE1006697A5/fr

Links

230000000855 fungicidal effect Effects 0.000 title claims abstract description 27
239000000417 fungicide Substances 0.000 title abstract description 20
239000000203 mixture Substances 0.000 claims abstract description 50
241000233866 Fungi Species 0.000 claims abstract description 10
238000000034 method Methods 0.000 claims abstract description 7
ZLIBICFPKPWGIZ-UHFFFAOYSA-N pyrimethanil Chemical compound CC1=CC(C)=NC(NC=2C=CC=CC=2)=N1 ZLIBICFPKPWGIZ-UHFFFAOYSA-N 0.000 claims abstract description 7
239000000126 substance Substances 0.000 claims abstract description 6
230000003032 phytopathogenic effect Effects 0.000 claims abstract description 3
150000001875 compounds Chemical class 0.000 claims description 31
-1 4-chlorphenoxy Chemical group 0.000 claims description 21
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
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 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 claims description 5
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
239000005741 Bromuconazole Substances 0.000 claims description 5
239000005747 Chlorothalonil Substances 0.000 claims description 5
239000005785 Fluquinconazole Substances 0.000 claims description 5
239000005867 Iprodione Substances 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
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 5
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 claims description 5
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 claims description 5
239000005794 Hymexazol Substances 0.000 claims description 4
239000005802 Mancozeb Substances 0.000 claims description 4
239000005820 Prochloraz Substances 0.000 claims description 4
239000005843 Thiram Substances 0.000 claims description 4
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 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
KGVPNLBXJKTABS-UHFFFAOYSA-N hymexazol Chemical compound CC1=CC(O)=NO1 KGVPNLBXJKTABS-UHFFFAOYSA-N 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
229960002447 thiram Drugs 0.000 claims description 4
239000005842 Thiophanate-methyl Substances 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 3
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 3
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 3
ZMYFCFLJBGAQRS-UHFFFAOYSA-N 1-{[3-(2-chlorophenyl)-2-(4-fluorophenyl)oxiran-2-yl]methyl}-1H-1,2,4-triazole Chemical compound C1=CC(F)=CC=C1C1(CN2N=CN=C2)C(C=2C(=CC=CC=2)Cl)O1 ZMYFCFLJBGAQRS-UHFFFAOYSA-N 0.000 claims description 2
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125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
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CLVALLQETQTQMV-UHFFFAOYSA-N 2-(1,2,4-triazol-1-yl)ethanol Chemical compound OCCN1C=NC=N1 CLVALLQETQTQMV-UHFFFAOYSA-N 0.000 claims 1
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LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
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241000722093 Tilletia caries Species 0.000 description 1
ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
APQHKWPGGHMYKJ-UHFFFAOYSA-N Tributyltin oxide Chemical compound CCCC[Sn](CCCC)(CCCC)O[Sn](CCCC)(CCCC)CCCC APQHKWPGGHMYKJ-UHFFFAOYSA-N 0.000 description 1
239000005858 Triflumizole Substances 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
CIUQDSCDWFSTQR-UHFFFAOYSA-N [C]1=CC=CC=C1 Chemical class [C]1=CC=CC=C1 CIUQDSCDWFSTQR-UHFFFAOYSA-N 0.000 description 1
HKNSIVFWRXBWCK-UHFFFAOYSA-N [N].NC1=CC=CC=C1 Chemical compound [N].NC1=CC=CC=C1 HKNSIVFWRXBWCK-UHFFFAOYSA-N 0.000 description 1
150000008061 acetanilides Chemical class 0.000 description 1
239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000003931 anilides Chemical class 0.000 description 1
150000008059 anilinopyrimidines Chemical class 0.000 description 1
230000003042 antagnostic effect Effects 0.000 description 1
235000021016 apples Nutrition 0.000 description 1
150000005840 aryl radicals Chemical class 0.000 description 1
AKNQMEBLVAMSNZ-UHFFFAOYSA-N azaconazole Chemical compound ClC1=CC(Cl)=CC=C1C1(CN2N=CN=C2)OCCO1 AKNQMEBLVAMSNZ-UHFFFAOYSA-N 0.000 description 1
229950000294 azaconazole Drugs 0.000 description 1
ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical class C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 description 1
JHRWWRDRBPCWTF-OLQVQODUSA-N captafol Chemical compound C1C=CC[C@H]2C(=O)N(SC(Cl)(Cl)C(Cl)Cl)C(=O)[C@H]21 JHRWWRDRBPCWTF-OLQVQODUSA-N 0.000 description 1
229940117949 captan Drugs 0.000 description 1
DKVNPHBNOWQYFE-UHFFFAOYSA-N carbamodithioic acid Chemical compound NC(S)=S DKVNPHBNOWQYFE-UHFFFAOYSA-N 0.000 description 1
239000006013 carbendazim Substances 0.000 description 1
JNPZQRQPIHJYNM-UHFFFAOYSA-N carbendazim Chemical compound C1=C[CH]C2=NC(NC(=O)OC)=NC2=C1 JNPZQRQPIHJYNM-UHFFFAOYSA-N 0.000 description 1
DHNRXBZYEKSXIM-UHFFFAOYSA-N chloromethylisothiazolinone Chemical compound CN1SC(Cl)=CC1=O DHNRXBZYEKSXIM-UHFFFAOYSA-N 0.000 description 1
235000020971 citrus fruits Nutrition 0.000 description 1
150000004699 copper complex Chemical class 0.000 description 1
229940120693 copper naphthenate Drugs 0.000 description 1
SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
239000006071 cream Substances 0.000 description 1
XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
230000017858 demethylation Effects 0.000 description 1
238000010520 demethylation reaction Methods 0.000 description 1
208000002925 dental caries Diseases 0.000 description 1
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 description 1
LNJNFVJKDJYTEU-UHFFFAOYSA-N diethofencarb Chemical compound CCOC1=CC=C(NC(=O)OC(C)C)C=C1OCC LNJNFVJKDJYTEU-UHFFFAOYSA-N 0.000 description 1
BQYJATMQXGBDHF-UHFFFAOYSA-N difenoconazole Chemical compound O1C(C)COC1(C=1C(=CC(OC=2C=CC(Cl)=CC=2)=CC=1)Cl)CN1N=CN=C1 BQYJATMQXGBDHF-UHFFFAOYSA-N 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
230000000694 effects Effects 0.000 description 1
239000003995 emulsifying agent Substances 0.000 description 1
229960002125 enilconazole Drugs 0.000 description 1
FKLFBQCQQYDUAM-UHFFFAOYSA-N fenpiclonil Chemical compound ClC1=CC=CC(C=2C(=CNC=2)C#N)=C1Cl FKLFBQCQQYDUAM-UHFFFAOYSA-N 0.000 description 1
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 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
PTCGDEVVHUXTMP-UHFFFAOYSA-N flutolanil Chemical compound CC(C)OC1=CC=CC(NC(=O)C=2C(=CC=CC=2)C(F)(F)F)=C1 PTCGDEVVHUXTMP-UHFFFAOYSA-N 0.000 description 1
HKIOYBQGHSTUDB-UHFFFAOYSA-N folpet Chemical compound C1=CC=C2C(=O)N(SC(Cl)(Cl)Cl)C(=O)C2=C1 HKIOYBQGHSTUDB-UHFFFAOYSA-N 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
AGKSTYPVMZODRV-UHFFFAOYSA-N imibenconazole Chemical compound C1=CC(Cl)=CC=C1CSC(CN1N=CN=C1)=NC1=CC=C(Cl)C=C1Cl AGKSTYPVMZODRV-UHFFFAOYSA-N 0.000 description 1
230000002401 inhibitory effect Effects 0.000 description 1
230000003993 interaction Effects 0.000 description 1
239000011872 intimate mixture Substances 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 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
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 description 1
150000004702 methyl esters Chemical class 0.000 description 1
BEGLCMHJXHIJLR-UHFFFAOYSA-N methylisothiazolinone Chemical compound CN1SC=CC1=O BEGLCMHJXHIJLR-UHFFFAOYSA-N 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
239000007764 o/w emulsion Substances 0.000 description 1
239000003960 organic solvent Substances 0.000 description 1
235000021017 pears Nutrition 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
XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical compound C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 description 1
235000012015 potatoes Nutrition 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
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
WZZLDXDUQPOXNW-UHFFFAOYSA-N propamocarb Chemical compound CCCOC(=O)NCCCN(C)C WZZLDXDUQPOXNW-UHFFFAOYSA-N 0.000 description 1
230000000069 prophylactic effect Effects 0.000 description 1
XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
239000002689 soil Substances 0.000 description 1
239000007787 solid Substances 0.000 description 1
238000004659 sterilization and disinfection Methods 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
239000000375 suspending agent Substances 0.000 description 1
DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-UHFFFAOYSA-N 0.000 description 1
HSMVPDGQOIQYSR-KGENOOAVSA-N triflumizole Chemical compound C1=CN=CN1C(/COCCC)=N/C1=CC=C(Cl)C=C1C(F)(F)F HSMVPDGQOIQYSR-KGENOOAVSA-N 0.000 description 1
239000004563 wettable powder Substances 0.000 description 1
239000000080 wetting agent 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)

BE9300573A 1992-06-10 1993-06-07 Melanges fongicides. BE1006697A5 (fr)

Applications Claiming Priority (3)

Application Number	Priority Date	Filing Date	Title
GB929212332A GB9212332D0 (en)	1992-06-10	1992-06-10	Fungicidal compositions
GB929212877A GB9212877D0 (en)	1992-06-17	1992-06-17	Fungicidal compositions
GB929222839A GB9222839D0 (en)	1992-10-30	1992-10-30	Fundicidal compositions

Publications (1)

Publication Number	Publication Date
BE1006697A5 true BE1006697A5 (fr)	1994-11-22

Family

ID=27266239

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
BE9300573A BE1006697A5 (fr)	1992-06-10	1993-06-07	Melanges fongicides.

Country Status (11)

Country	Link
JP (1)	JP3643386B2 (de)
AT (1)	AT402878B (de)
AU (1)	AU659016B2 (de)
BE (1)	BE1006697A5 (de)
DE (1)	DE4318372B4 (de)
FR (1)	FR2692108B1 (de)
HU (1)	HU212898B (de)
IL (1)	IL105941A (de)
IT (1)	IT1268412B1 (de)
NL (1)	NL194531C (de)
PL (1)	PL172180B1 (de)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
TW286264B (de) *	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 (de) *	2002-10-24	2004-04-28	Bayer CropScience SA	Verwendung von Pyrimethanil gegen resistente Pathogene
CA2554236C (en) *	2004-02-04	2012-09-11	Janssen Pharmaceutica N.V.	Synergistic antifungal didecyl dimethyl ammonium chloride compositions
EP1570737A1 (de) *	2004-02-12	2005-09-07	Bayer CropScience S.A.	Fungizide Zusammensetzung enthaltend ein Pyridylethylbenzamidderivat und eine Methioninbiosynthesehemmende Verbindung
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 (de) *	2007-09-07	2011-07-13	Janssen Pharmaceutica NV	Kombinationen aus pyrimethanil und silberverbindungen
AR071344A1 (es) *	2008-02-05	2010-06-16	Basf Se	Mezclas de plaguicidas
EP2253206B1 (de) *	2008-03-21	2014-01-01	Sumitomo Chemical Company, Limited	Zusammensetzung für die bekämpfung von pflanzenkrankheiten
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 (de) *	2019-10-16	2021-04-21	LANXESS Deutschland GmbH	Fungizide mischungen
EP3808178B1 (de) *	2019-10-16	2024-12-11	LANXESS Deutschland GmbH	Fungizide mischungen

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DD151404A1 (de) *	1980-06-13	1981-10-21	Friedrich Franke	Fungizide mittel
JPH0578211A (ja) *	1991-09-18	1993-03-30	Kaiyo Kagaku Kk	水中生物防汚剤
JPH0578214A (ja) *	1991-02-07	1993-03-30	Kumiai Chem Ind Co Ltd	農園芸用殺菌剤組成物
JPH05112408A (ja) *	1991-03-20	1993-05-07	Kumiai Chem Ind Co Ltd	農園芸用殺菌剤組成物
EP0556157A1 (de) *	1992-02-13	1993-08-18	Ciba-Geigy Ag	Fungizide Mischungen auf der Basis von Triazol-Fungiziden und 4,6-Dimethyl-N-Phenyl-2-Pyrimidinamin

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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

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

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DD151404A1 (de) *	1980-06-13	1981-10-21	Friedrich Franke	Fungizide mittel
JPH0578214A (ja) *	1991-02-07	1993-03-30	Kumiai Chem Ind Co Ltd	農園芸用殺菌剤組成物
JPH05112408A (ja) *	1991-03-20	1993-05-07	Kumiai Chem Ind Co Ltd	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
EP0556157A1 (de) *	1992-02-13	1993-08-18	Ciba-Geigy Ag	Fungizide Mischungen auf der Basis von Triazol-Fungiziden und 4,6-Dimethyl-N-Phenyl-2-Pyrimidinamin

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CHEMICAL PATENTS INDEX, DOCUMENTATION ABSTRACTS JOURNAL Week 9323, Derwent World Patents Index; AN 93-185134/23 *

Also Published As

Publication number	Publication date
NL194531C (nl)	2002-07-02
DE4318372B4 (de)	2010-10-28
HU9301686D0 (en)	1993-09-28
PL172180B1 (pl)	1997-08-29
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

Legal Events

Date

Code

Title

Description

2013-06-30

RE20

Patent expired

Owner name: *BASF AGRO B.V.

Effective date: 20130607

Publication	Publication Date	Title
BE1006697A5 (fr)	1994-11-22	Melanges fongicides.
GB2267644A (en)	1993-12-15	Mixed class synergistic fungicide based on pyrimethanil
JP4127853B2 (ja)	2008-07-30	殺菌剤混合物
JP3866286B2 (ja)	2007-01-10	農作物保護性製品
JPH0624914A (ja)	1994-02-01	殺生物剤
CZ293009B6 (cs)	2004-01-14	Fungicidní směs a způsob potírání škodlivých hub
EP0040007B1 (de)	1983-05-18	Fungizide Mischungen
RU2129371C1 (ru)	1999-04-27	Фунгицидная композиция, способ борьбы с фитопатогенными грибами
EP3078267A1 (de)	2016-10-12	Landwirtschaftliche und gärtnerische präparate, verfahren zur bekämpfung von pflanzenkrankheiten und produkt zur bekämpfung von pflanzenkrankheiten
BE1005834A5 (fr)	1994-02-15	Nouvelles compositions fongicides a base d'inhibiteurs de la biosynthese des sterols.
JPH11511143A (ja)	1999-09-28	殺菌剤混合物
CH636501A5 (fr)	1983-06-15	Composition fongicide synergique.
US6495572B1 (en)	2002-12-17	Synergistic mixtures of an amino acid
EP0072156B1 (de)	1984-11-28	Prochloraz enthaltende fungizide Zusammensetzungen
CZ375397A3 (cs)	1998-05-13	Fungicidní prostředek, jeho použití a způsob potírání hub
EP1021088B1 (de)	2003-05-07	Fungizide zusammensetzungen auf der basis von fluquinconazole
EP0106558B1 (de)	1987-07-29	Fungizide Mischungen
EP0280431A1 (de)	1988-08-31	Fungizide Mischungen mit Prochloraz
EP0290204A1 (de)	1988-11-09	Fungizide Mischungen mit Prochloraz
EP0647400A1 (de)	1995-04-12	Fungizide Mischungen
EP0433194A1 (de)	1991-06-19	Fungizide Zusammensetzung mit synergetischer Wirkung auf der Basis von einem Morpholin und einem Triazol
JPH0443041B2 (de)	1992-07-15
WO2006009967A2 (en)	2006-01-26	Novel ester as useful broad spectrum fungicidal compounds