UA80509C2 - Fungicidal mixture, means, method for control, sowing material and use of compounds - Google Patents

Fungicidal mixture, means, method for control, sowing material and use of compounds Download PDF

Info

Publication number: UA80509C2
Authority: UA; Ukraine
Prior art keywords: compounds; compound; formula; mixtures; mixture
Prior art date: 2004-03-30

Application number

UAA200609160A

Other languages

English (en)

Ukrainian (uk)

Inventor

I Blasco Tormo

Thomas Grotte

Maria Scherer

Reinhard Stierl

Siegfried Strathmann

Ulrich Schoefl

Original Assignee

Basf 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.)

2004-03-30

Filing date

2005-01-14

Publication date

2007-09-25

2005-01-14 Application filed by Basf Ag filed Critical Basf Ag

2005-01-14 Priority claimed from PCT/EP2005/000313 external-priority patent/WO2005067716A1/fr

2007-09-25 Publication of UA80509C2 publication Critical patent/UA80509C2/uk

Links

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NCXMLFZGDNKEPB-FFPOYIOWSA-N natamycin Chemical compound O[C@H]1[C@@H](N)[C@H](O)[C@@H](C)O[C@H]1O[C@H]1/C=C/C=C/C=C/C=C/C[C@@H](C)OC(=O)/C=C/[C@H]2O[C@@H]2C[C@H](O)C[C@](O)(C[C@H](O)[C@H]2C(O)=O)O[C@H]2C1 NCXMLFZGDNKEPB-FFPOYIOWSA-N 0.000 description 1
239000004311 natamycin Substances 0.000 description 1
235000010298 natamycin Nutrition 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
239000010742 number 1 fuel oil Substances 0.000 description 1
125000001209 o-nitrophenyl group Chemical group [H]C1=C([H])C(*)=C(C([H])=C1[H])[N+]([O-])=O 0.000 description 1
JHIPUJPTQJYEQK-ZLHHXESBSA-N orysastrobin Chemical compound CNC(=O)C(=N\OC)\C1=CC=CC=C1CO\N=C(/C)\C(=N\OC)\C(\C)=N\OC JHIPUJPTQJYEQK-ZLHHXESBSA-N 0.000 description 1
UWVQIROCRJWDKL-UHFFFAOYSA-N oxadixyl Chemical compound CC=1C=CC=C(C)C=1N(C(=O)COC)N1CCOC1=O UWVQIROCRJWDKL-UHFFFAOYSA-N 0.000 description 1
AMEKQAFGQBKLKX-UHFFFAOYSA-N oxycarboxin Chemical compound O=S1(=O)CCOC(C)=C1C(=O)NC1=CC=CC=C1 AMEKQAFGQBKLKX-UHFFFAOYSA-N 0.000 description 1
239000012188 paraffin wax Substances 0.000 description 1
LKPLKUMXSAEKID-UHFFFAOYSA-N pentachloronitrobenzene Chemical compound [O-][N+](=O)C1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl LKPLKUMXSAEKID-UHFFFAOYSA-N 0.000 description 1
239000000575 pesticide Substances 0.000 description 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
IBSNKSODLGJUMQ-SDNWHVSQSA-N picoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=CC(C(F)(F)F)=N1 IBSNKSODLGJUMQ-SDNWHVSQSA-N 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
229920000090 poly(aryl ether) Polymers 0.000 description 1
YEBIHIICWDDQOL-YBHNRIQQSA-N polyoxin Polymers O[C@@H]1[C@H](O)[C@@H](C(C=O)N)O[C@H]1N1C(=O)NC(=O)C(C(O)=O)=C1 YEBIHIICWDDQOL-YBHNRIQQSA-N 0.000 description 1
229920001451 polypropylene glycol Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 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
BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-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
KKMLIVYBGSAJPM-UHFFFAOYSA-L propineb Chemical compound [Zn+2].[S-]C(=S)NC(C)CNC([S-])=S KKMLIVYBGSAJPM-UHFFFAOYSA-L 0.000 description 1
FLVBXVXXXMLMOX-UHFFFAOYSA-N proquinazid Chemical compound C1=C(I)C=C2C(=O)N(CCC)C(OCCC)=NC2=C1 FLVBXVXXXMLMOX-UHFFFAOYSA-N 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
XRJLAOUDSILTFT-UHFFFAOYSA-N pyroquilon Chemical compound O=C1CCC2=CC=CC3=C2N1CC3 XRJLAOUDSILTFT-UHFFFAOYSA-N 0.000 description 1
150000004040 pyrrolidinones Chemical class 0.000 description 1
229920006395 saturated elastomer Polymers 0.000 description 1
RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
235000012239 silicon dioxide 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
239000004550 soluble concentrate Substances 0.000 description 1
239000000600 sorbitol Substances 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
238000001694 spray drying Methods 0.000 description 1
235000021012 strawberries Nutrition 0.000 description 1
229960005322 streptomycin Drugs 0.000 description 1
150000003460 sulfonic acids Chemical class 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
239000004094 surface-active agent Substances 0.000 description 1
LITQZINTSYBKIU-UHFFFAOYSA-F tetracopper;hexahydroxide;sulfate Chemical compound [OH-].[OH-].[OH-].[OH-].[OH-].[OH-].[Cu+2].[Cu+2].[Cu+2].[Cu+2].[O-]S([O-])(=O)=O LITQZINTSYBKIU-UHFFFAOYSA-F 0.000 description 1
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 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
235000010296 thiabendazole Nutrition 0.000 description 1
229960004546 thiabendazole Drugs 0.000 description 1
WOSNCVAPUOFXEH-UHFFFAOYSA-N thifluzamide Chemical compound S1C(C)=NC(C(F)(F)F)=C1C(=O)NC1=C(Br)C=C(OC(F)(F)F)C=C1Br WOSNCVAPUOFXEH-UHFFFAOYSA-N 0.000 description 1
QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
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 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
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
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
RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
150000003672 ureas Chemical class 0.000 description 1
239000004562 water dispersible granule Substances 0.000 description 1
239000004552 water soluble powder Substances 0.000 description 1
239000003021 water soluble solvent Substances 0.000 description 1
238000009736 wetting Methods 0.000 description 1
DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 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
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
- 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
- A01N37/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
- A01N37/44—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids
- A01N37/50—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a nitrogen atom attached to the same carbon skeleton by a single or double bond, this nitrogen atom not being a member of a derivative or of a thio analogue of a carboxylic group, e.g. amino-carboxylic acids the nitrogen atom being doubly bound to the carbon skeleton
- 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)
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)

UAA200609160A 2004-03-30 2005-01-14 Fungicidal mixture, means, method for control, sowing material and use of compounds UA80509C2 (en)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE102004016084		2004-03-30
PCT/EP2005/000313 WO2005067716A1 (fr)	2004-01-20	2005-01-14	Melanges fongicides

Publications (1)

Publication Number	Publication Date
UA80509C2 true UA80509C2 (en)	2007-09-25

Family

ID=34963344

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
UAA200609160A UA80509C2 (en)	2004-03-30	2005-01-14	Fungicidal mixture, means, method for control, sowing material and use of compounds
UAA200611305A UA80931C2 (en)	2004-03-30	2005-03-26	Ternary fungicidal mixture, an agent, a method for controlling, an inoculum and the use of compounds

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
UAA200611305A UA80931C2 (en)	2004-03-30	2005-03-26	Ternary fungicidal mixture, an agent, a method for controlling, an inoculum and the use of compounds

Country Status (19)

Country	Link
US (1)	US20110136665A1 (fr)
EP (1)	EP1732388A1 (fr)
JP (1)	JP2007537156A (fr)
KR (1)	KR20070004068A (fr)
CN (1)	CN1937920A (fr)
AR (1)	AR049375A1 (fr)
AU (1)	AU2005227688A1 (fr)
BR (1)	BRPI0508965A (fr)
CA (1)	CA2558062A1 (fr)
EA (1)	EA200601674A1 (fr)
EC (3)	ECSP066617A (fr)
IL (1)	IL177654A0 (fr)
MA (1)	MA28540B1 (fr)
NO (1)	NO20064923L (fr)
TW (1)	TW200601972A (fr)
UA (2)	UA80509C2 (fr)
UY (1)	UY28832A1 (fr)
WO (1)	WO2005094583A1 (fr)
ZA (1)	ZA200608907B (fr)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
CA2589646A1 (fr) *	2004-12-20	2006-06-29	Basf Aktiengesellschaft	Procede pour lutter contre les mycoses chez les legumineuses
AU2006211239B2 (en) *	2005-02-04	2011-04-07	Mitsui Chemicals, Inc.	Composition for preventing plant diseases and method for preventing the diseases
GB0508993D0 (en)	2005-05-03	2005-06-08	Syngenta Participations Ag	Pesticidal compositions
ES2383327T3 (es) *	2005-11-10	2012-06-20	Basf Se	Uso de pyraclostrobin como protector para triticonazol en el control de hongos nocivos
WO2007134777A2 (fr) *	2006-05-24	2007-11-29	Bayer Cropscience Ag	Combinaisons de principes actifs fongicides
DE102006024925A1 (de) *	2006-05-24	2007-11-29	Bayer Cropscience Ag	Fungizide Wirkstoffkombinationen
EP2109366A2 (fr) *	2007-02-06	2009-10-21	Basf Se	Mélanges pesticides
KR101182617B1 (ko) *	2007-08-06	2012-09-17	닛뽕소다 가부시키가이샤	농약 조성물, 농원예용 살균제 및 식물 병해의 방제 방법
JP2010540495A (ja) *	2007-09-26	2010-12-24	ビーエーエスエフソシエタス・ヨーロピア	ボスカリド及びクロロタロニルを含む三成分殺菌組成物
EP2242371A2 (fr) *	2008-02-05	2010-10-27	Basf Se	Mélanges pesticides
JP5359224B2 (ja) *	2008-11-25	2013-12-04	住友化学株式会社	植物病害防除用組成物及び植物病害の防除方法
CN101779660B (zh) *	2009-12-16	2013-03-20	福建新农大正生物工程有限公司	含有代森联的杀菌组合物
CN102150661A (zh) *	2011-02-25	2011-08-17	陕西美邦农药有限公司	一种含有氰霜唑与三唑类化合物的杀菌组合物
JP5776294B2 (ja) *	2011-04-15	2015-09-09	住友化学株式会社	有害節足動物防除組成物及び有害節足動物の防除方法
JP5997931B2 (ja)	2011-05-25	2016-09-28	石原産業株式会社	農園芸用殺菌剤組成物及び植物病害の防除方法
CN104322521B (zh) *	2012-11-15	2016-03-16	江苏扬农化工股份有限公司	一种含有氟啶胺的复配杀菌组合物
CN103210937A (zh) *	2013-02-06	2013-07-24	吉林省八达农药有限公司	一种含有丁香菌酯与其它杀菌剂的组合物
GB2519982B (en) *	2013-11-04	2016-04-27	Rotam Agrochem Int Co Ltd	Fungicidal composition and the use thereof
CN103783055B (zh) *	2014-02-28	2015-09-23	浙江农林大学	含啶酰菌胺的三元复配杀菌剂及其用途
CN104126595B (zh) *	2014-08-21	2016-04-13	陕西上格之路生物科学有限公司	一种含有吡唑醚菌酯的杀菌剂组合物
CN105941395A (zh) *	2016-04-30	2016-09-21	广东中迅农科股份有限公司	含有吡唑醚菌酯和咪鲜胺的农药组合物
RU2731294C1 (ru) *	2019-09-18	2020-09-01	ООО "Агро Эксперт Груп"	Фунгицидная композиция для обработки зерновых культур

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
SK283401B6 (sk) *	1996-08-30	2003-07-01	Basf Aktiengesellschaft	Fungicídne zmesi a spôsob ničenia škodlivých húb
TWI252231B (en) *	1997-04-14	2006-04-01	American Cyanamid Co	Fungicidal trifluorophenyl-triazolopyrimidines
CO5040026A1 (es) *	1997-05-28	2001-05-29	Basf Ag	Mezclas fungicidas que comprenden carbamatos y una sustancia activa aromatica que contiene fluor o cloro
EP1065928A1 (fr) *	1998-03-24	2001-01-10	Basf Aktiengesellschaft	Melanges fongicides a base de derives d'oximether de diatomite et de fongicides du riz
ATE240648T1 (de) *	1998-09-25	2003-06-15	Basf Ag	Fungizide mischungen
DE10063046A1 (de) *	2000-12-18	2002-06-20	Basf Ag	Fungizide Mischungen
US7687434B2 (en) *	2000-12-22	2010-03-30	Monsanto Technology, Llc	Method of improving yield and vigor of plants
WO2002054870A2 (fr) *	2001-01-16	2002-07-18	Basf Aktiengesellschaft	Mélanges fongicides
EA005609B1 (ru) *	2001-01-18	2005-04-28	Басф Акциенгезельшафт	Фунгицидные смеси
MXPA05004370A (es) *	2002-11-15	2005-07-26	Basf Ag	Mezclas fungicidas para combatir patogenos de arroz.
OA12957A (en) *	2002-11-15	2006-10-13	Basf Ag	Fungicidal mixtures.

2005
- 2005-01-14 UA UAA200609160A patent/UA80509C2/uk unknown
- 2005-03-26 BR BRPI0508965-4A patent/BRPI0508965A/pt not_active IP Right Cessation
- 2005-03-26 EA EA200601674A patent/EA200601674A1/ru unknown
- 2005-03-26 JP JP2007505466A patent/JP2007537156A/ja not_active Withdrawn
- 2005-03-26 WO PCT/EP2005/003213 patent/WO2005094583A1/fr not_active Ceased
- 2005-03-26 EP EP05729121A patent/EP1732388A1/fr not_active Withdrawn
- 2005-03-26 US US10/591,290 patent/US20110136665A1/en not_active Abandoned
- 2005-03-26 CN CNA2005800106414A patent/CN1937920A/zh active Pending
- 2005-03-26 UA UAA200611305A patent/UA80931C2/uk unknown
- 2005-03-26 AU AU2005227688A patent/AU2005227688A1/en not_active Abandoned
- 2005-03-26 KR KR1020067022407A patent/KR20070004068A/ko not_active Withdrawn
- 2005-03-26 CA CA002558062A patent/CA2558062A1/fr not_active Abandoned
- 2005-03-30 AR ARP050101251A patent/AR049375A1/es not_active Application Discontinuation
- 2005-03-30 TW TW094110054A patent/TW200601972A/zh unknown
- 2005-03-30 UY UY28832A patent/UY28832A1/es unknown
2006
- 2006-06-08 EC EC2006006617A patent/ECSP066617A/es unknown
- 2006-08-23 IL IL177654A patent/IL177654A0/en unknown
- 2006-09-28 EC EC2006006891A patent/ECSP066891A/es unknown
- 2006-09-28 EC EC2006006890A patent/ECSP066890A/es unknown
- 2006-10-18 MA MA29395A patent/MA28540B1/fr unknown
- 2006-10-27 NO NO20064923A patent/NO20064923L/no not_active Application Discontinuation
- 2006-10-27 ZA ZA200608907A patent/ZA200608907B/xx unknown

Also Published As

Publication number	Publication date
ECSP066891A (es)	2006-12-29
US20110136665A1 (en)	2011-06-09
IL177654A0 (en)	2006-12-31
WO2005094583A1 (fr)	2005-10-13
KR20070004068A (ko)	2007-01-05
BRPI0508965A (pt)	2007-08-21
CA2558062A1 (fr)	2005-10-13
EA200601674A1 (ru)	2007-04-27
TW200601972A (en)	2006-01-16
CN1937920A (zh)	2007-03-28
UA80931C2 (en)	2007-11-12
AU2005227688A1 (en)	2005-10-13
ECSP066890A (es)	2006-12-29
EP1732388A1 (fr)	2006-12-20
JP2007537156A (ja)	2007-12-20
NO20064923L (no)	2006-10-27
ECSP066617A (es)	2006-10-25
ZA200608907B (en)	2008-07-30
MA28540B1 (fr)	2007-04-03
AR049375A1 (es)	2006-07-26
UY28832A1 (es)	2005-10-31

Publication	Publication Date	Title
UA80509C2 (en)	2007-09-25	Fungicidal mixture, means, method for control, sowing material and use of compounds
JP2007502850A (ja)	2007-02-15	イネ病原体を防除するための殺菌混合物
MX2007005510A (es)	2007-07-20	Procedimiento para intensificar la eficiencia de etaboxam.
UA81176C2 (en)	2007-12-10	Fungicidal mixture containing triazolopyrimidine derivative and epoxiconazole, agent, method for controlling pathogenous fungi from class oomycetes and seed
UA80659C2 (en)	2007-10-10	Fungicidal mixture, agent, method for controlling phytopathogenic fungi, sowing material and use of compounds
EA008738B1 (ru)	2007-08-31	Фунгицидные смеси
JP2007505852A (ja)	2007-03-15	殺菌混合物
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