NO313458B1 - Pesticide blanding, forbindelse og fremgangsmåte for å kontrollere insekter - Google Patents

Pesticide blanding, forbindelse og fremgangsmåte for å kontrollere insekter Download PDF

Info

Publication number: NO313458B1
Authority: NO; Norway
Prior art keywords: acetyl; dichloro; trifluoromethylphenyl; methylsulfinylpyrazole; amino
Prior art date: 1996-12-24

Application number

NO19993107A

Other languages

English (en)

Norwegian (no)

Other versions

NO993107D0 (no

NO993107L (no

Inventor

Jennifer Phillips

Michael Pilato

Tai-Teh Wu

Original Assignee

Rhone Poulenc Agro Sa

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.)

1996-12-24

Filing date

1999-06-22

Publication date

2002-10-07

1999-06-22 Application filed by Rhone Poulenc Agro Sa filed Critical Rhone Poulenc Agro Sa

1999-06-22 Publication of NO993107D0 publication Critical patent/NO993107D0/no

1999-08-24 Publication of NO993107L publication Critical patent/NO993107L/no

2002-10-07 Publication of NO313458B1 publication Critical patent/NO313458B1/no

Links

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UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 1
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150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
YBBRCQOCSYXUOC-UHFFFAOYSA-N sulfuryl dichloride Chemical compound ClS(Cl)(=O)=O YBBRCQOCSYXUOC-UHFFFAOYSA-N 0.000 description 1
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CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
IOGXOCVLYRDXLW-UHFFFAOYSA-N tert-butyl nitrite Chemical compound CC(C)(C)ON=O IOGXOCVLYRDXLW-UHFFFAOYSA-N 0.000 description 1
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MLGCXEBRWGEOQX-UHFFFAOYSA-N tetradifon Chemical compound C1=CC(Cl)=CC=C1S(=O)(=O)C1=CC(Cl)=C(Cl)C=C1Cl MLGCXEBRWGEOQX-UHFFFAOYSA-N 0.000 description 1
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YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
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230000001988 toxicity Effects 0.000 description 1
AMFGTOFWMRQMEM-UHFFFAOYSA-N triazophos Chemical compound N1=C(OP(=S)(OCC)OCC)N=CN1C1=CC=CC=C1 AMFGTOFWMRQMEM-UHFFFAOYSA-N 0.000 description 1
QORWJWZARLRLPR-UHFFFAOYSA-H tricalcium bis(phosphate) Chemical compound [Ca+2].[Ca+2].[Ca+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O QORWJWZARLRLPR-UHFFFAOYSA-H 0.000 description 1
229940078499 tricalcium phosphate Drugs 0.000 description 1
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NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
RQYLOOVORNJDQX-UHFFFAOYSA-N trifluoromethyl thiohypochlorite Chemical compound FC(F)(F)SCl RQYLOOVORNJDQX-UHFFFAOYSA-N 0.000 description 1
230000001960 triggered effect Effects 0.000 description 1
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Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
- 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
- A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
- 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
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
- 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
- A01N47/02—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 no bond to a nitrogen atom
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/44—Oxygen and nitrogen or sulfur and nitrogen atoms
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
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)
Plural Heterocyclic Compounds (AREA)

NO19993107A 1996-12-24 1999-06-22 Pesticide blanding, forbindelse og fremgangsmåte for å kontrollere insekter NO313458B1 (no)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
US3388796P	1996-12-24	1996-12-24
PCT/EP1997/007115 WO1998028277A1 (fr)	1996-12-24	1997-12-18	1-arylpyrazoles pesticides

Publications (3)

Publication Number	Publication Date
NO993107D0 NO993107D0 (no)	1999-06-22
NO993107L NO993107L (no)	1999-08-24
NO313458B1 true NO313458B1 (no)	2002-10-07

Family

ID=21873039

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
NO19993107A NO313458B1 (no)	1996-12-24	1999-06-22	Pesticide blanding, forbindelse og fremgangsmåte for å kontrollere insekter

Country Status (37)

Country	Link
US (2)	US6087387A (fr)
EP (1)	EP0948486B1 (fr)
JP (1)	JP2001506664A (fr)
KR (1)	KR20000062319A (fr)
CN (1)	CN1099415C (fr)
AP (1)	AP1237A (fr)
AR (1)	AR011048A1 (fr)
AU (1)	AU746514B2 (fr)
BG (1)	BG64857B1 (fr)
BR (1)	BR9714181A (fr)
CA (1)	CA2275635C (fr)
CO (1)	CO5031287A1 (fr)
CU (1)	CU22869A3 (fr)
CZ (1)	CZ294766B6 (fr)
DE (1)	DE69738328T2 (fr)
DK (1)	DK0948486T3 (fr)
EA (1)	EA002085B1 (fr)
EE (1)	EE05495B1 (fr)
EG (1)	EG21715A (fr)
ES (1)	ES2297867T3 (fr)
HR (1)	HRP970703B1 (fr)
HU (1)	HU229905B1 (fr)
ID (1)	ID19248A (fr)
IL (1)	IL130533A (fr)
MA (1)	MA24432A1 (fr)
MY (1)	MY128485A (fr)
NO (1)	NO313458B1 (fr)
NZ (1)	NZ336418A (fr)
OA (1)	OA11133A (fr)
PL (1)	PL193231B1 (fr)
PT (1)	PT948486E (fr)
RS (1)	RS49966B (fr)
SK (1)	SK285866B6 (fr)
TR (1)	TR199901473T2 (fr)
TW (1)	TW505503B (fr)
WO (1)	WO1998028277A1 (fr)
ZA (1)	ZA9711590B (fr)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
AP1237A (en)	1996-12-24	2004-01-14	Merial Ltd	Pesticidal 1-arylpyrazoles.
US6531501B1 (en)	1998-12-11	2003-03-11	Aventis Cropscience, S.A.	Control of arthropods in animals
AR021608A1 (es) *	1998-12-11	2002-07-31	Merial Ltd	Represion de artropodos en animales
CN1939909A (zh)	1999-12-02	2007-04-04	阿温提斯作物科学股份有限公司	控制动物中的节肢动物
HUP0301672A3 (en) *	2000-06-09	2005-01-28	Merial Ltd	Process for the preparation of pesticidal compounds
AU2003221298B2 (en) *	2002-03-05	2009-02-19	Boehringer Ingelheim Animal Health USA Inc.	5-substituted-alkylaminopyrazole derivatives as pesticides
CN101043815A (zh) *	2004-10-22	2007-09-26	巴斯福股份公司	杀虫混合物
ES2444016T3 (es) *	2004-11-11	2014-02-21	Merial Limited	Derivados de vinilaminopirazol como pesticidas
CA2632021A1 (fr) *	2005-12-23	2007-06-28	Astrazeneca Ab	Modulateurs des recepteurs gaba-b
JP5424874B2 (ja)	2006-06-22	2014-02-26	ビーエーエスエフソシエタス・ヨーロピア	マロノニトリル化合物
EP2465851A1 (fr) *	2006-07-05	2012-06-20	Aventis Agriculture	Composés dérivés de 1-aryl-5-alkyl pyrazole, leurs procédés de fabrication et leurs procédés d'utilisation
AU2012203942B2 (en) *	2006-07-05	2014-11-27	Boehringer Ingelheim Animal Health USA Inc.	1-aryl-5-alkyl pyrazole derivative compounds, processes of making and methods of using thereof
CN101534650B (zh)	2006-09-14	2014-06-11	巴斯夫欧洲公司	杀虫剂组合物
US8791046B2 (en)	2006-11-10	2014-07-29	Basf Se	Crystalline modification of fipronil
UA110598C2 (uk)	2006-11-10	2016-01-25	Басф Се	Спосіб одержання кристалічної модифікації фіпронілу
BRPI0718717A2 (pt)	2006-11-10	2013-11-26	Basf Se	Modificação cristalina ii de fipronil, fipronil sólido, processo para preparar a modificação cristalina ii, mistura pesticida ou parasiticida sinergística, composição pesticida ou parasiticida, uso da modificação cristalina ii, ou do fipronil sólido, ou da mistura, ou da composição, métodos para controlar pragas, para proteger uma planta da infestação e ataque por pragas, para proteger semente, e para tratar, controlar, prevenir ou proteger animais contra infestação ou infecção por parasitas, semente, uso da modificação cristalina ii, ou do fipronil sólido, ou da mistura, ou da composição, e, processo para a preparação de uma composição para trtar, controlar, prevenir ou proteger animais contra infestação ou infecção por parasitas
JP5931322B2 (ja)	2006-11-10	2016-06-08	ビーエーエスエフソシエタス・ヨーロピアＢａｓｆＳｅ	フィプロニルの結晶変態
DE602007008754D1 (de)	2006-11-30	2010-10-07	Basf Se	Landwirtschaftliche formulierungen mit copolymeren auf basis von diisocyanaten
EA200900654A1 (ru)	2006-11-30	2009-12-30	Басф Се	Агрохимические композиции, содержащие сополимеры 1-винил-2-пирролидинона
CA2668564A1 (fr)	2006-11-30	2008-06-05	Basf Se	Preparations agrochimiques contenant des copolymeres n-vinylamide
EP2164323A1 (fr)	2006-12-15	2010-03-24	Rohm and Haas Company	Mélanges comprenant du 1-méthylcyclopropène
DE102006061537A1 (de)	2006-12-27	2008-07-03	Bayer Healthcare Ag	Mittel zur Bekämpfung von Parasiten an Tieren
DE102006061538A1 (de) *	2006-12-27	2008-07-03	Bayer Healthcare Ag	Kombinationsprodukt zur Bekämpfung von Parasiten an Tieren
AU2008206921B2 (en)	2007-01-19	2012-11-01	Basf Se	Fungicidal mixtures of 1-methylpyrazole-4-ylcarboxylic acid anilides and azolopyrimidinylamines
KR20090107070A (ko)	2007-01-26	2009-10-12	바스프 에스이	동물 해충 ⅱ의 퇴치를 위한 3-아미노-1,2-벤즈이소티아졸 화합물
EP1952690A3 (fr)	2007-01-31	2009-04-22	Basf Se	Mélanges de pesticides basés sur des triazolopyrimidines et des insecticides
EP2679094A1 (fr)	2007-02-06	2014-01-01	Basf Se	Mélanges de pesticides
CN104206402B (zh)	2007-04-12	2018-04-24	巴斯夫欧洲公司	包含氰基亚磺酰亚胺基化合物的农药混合物
CA2682294A1 (fr)	2007-04-23	2008-10-30	Basf Se	Augmentation de la productivite d'une plante par combinaison d'agents chimiques avec des modifications transgeniques
MX2010001666A (es)	2007-08-16	2010-03-10	Basf Se	Composiciones y metodos para el tratamiento de semillas.
EA201000324A1 (ru) *	2007-08-17	2010-10-29	Басф Се	Инсектициды для увеличения урожайности
NZ600929A (en)	2007-09-20	2014-02-28	Basf Se	Combinations comprising a fungicidal strain and an active compound
EP2500340A1 (fr)	2008-01-25	2012-09-19	Syngenta Participations AG.	Dérives de 2-cyanophenyl sulfonamide en tant que pesticides
US9173728B2 (en)	2008-11-19	2015-11-03	Merial Inc.	Multi-cavity container having offset indentures for dispensing fluids
MY155497A (en)	2008-11-19	2015-10-30	Merial Inc	Compositions comprising an aryl pyrazole and/or a formamidine, methods and use thereof
US20110256200A1 (en)	2008-12-23	2011-10-20	Basf Se	Process and aqueous formulation for the impregnation of non-living-materials imparting a protective activity against pests
WO2011003796A1 (fr)	2009-07-06	2011-01-13	Basf Se	Composés pyridazine destinés à la lutte contre les nuisibles invertébrés
EP2550264B1 (fr)	2010-03-23	2016-06-08	Basf Se	COMPOSÉS PYRIDAZINE DESTINÉS À LA LUTTE CONTRE LES NUISIBLES & xA; INVERTÉBRÉS
WO2013000572A1 (fr)	2011-06-30	2013-01-03	2LUTION GmbH	Agents de lutte contre les parasites d'animaux
JO3626B1 (ar)	2012-02-23	2020-08-27	Merial Inc	تركيبات موضعية تحتوي على فيبرونيل و بيرميثرين و طرق استخدامها
CN104370818B (zh) *	2014-11-10	2017-04-05	浙江海正化工股份有限公司	一种氧化法制备乙虫腈的工艺
CN106866537A (zh) *	2017-04-19	2017-06-20	江苏托球农化股份有限公司	一种乙虫腈的生产工艺
CN109651343B (zh) *	2019-01-07	2020-06-19	中南民族大学	一种氟虫腈吡唑醇环酰亚胺化合物及其微波水热法方法与应用
WO2025242701A1 (fr)	2024-05-22	2025-11-27	Basf Se	Compositions de traitement de semences

Family Cites Families (19)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3602728A1 (de) *	1985-05-17	1986-11-20	Bayer Ag, 51373 Leverkusen	Schaedlingsbekaempfungsmittel auf basis von pyrazolderivaten
GB8531485D0 (en) *	1985-12-20	1986-02-05	May & Baker Ltd	Compositions of matter
GB8713768D0 (en) *	1987-06-12	1987-07-15	May & Baker Ltd	Compositions of matter
US5232940A (en) *	1985-12-20	1993-08-03	Hatton Leslie R	Derivatives of N-phenylpyrazoles
US4918085A (en) *	1989-03-02	1990-04-17	Rhone-Poulenc Ag Company	Pesticidal 3-cyano-5-alkoxy-1-arylpyrazoles, compositions and use
YU47834B (sr) *	1989-08-10	1996-01-09	Schering Agrochemical Limited	Azolni pesticid
IL101702A (en) *	1991-04-30	1996-03-31	Rhone Poulenc Agrochimie	1-aryl-5-(substituted alkylideneimino)-pyrazoles process for their preparation and arthropodicidal nematodicidal helminthicidal and protozoocidal compositions containing them
GB9120641D0 (en) *	1991-09-27	1991-11-06	Ici Plc	Heterocyclic compounds
EP0680341B1 (fr) *	1993-01-25	2001-05-09	Sonus Pharmaceuticals, Inc.	Colloides a decalage de phase utiles comme agents de contraste ultrasonores
GB9306184D0 (en) *	1993-03-25	1993-05-19	Zeneca Ltd	Heteroaromatic compounds
US5798091A (en) *	1993-07-30	1998-08-25	Alliance Pharmaceutical Corp.	Stabilized gas emulsion containing phospholipid for ultrasound contrast enhancement
EP1550464A1 (fr) *	1993-07-30	2005-07-06	IMCOR Pharmaceutical Co.	Composition à microbulles stabilisées pour application mettant en oeuvre des ultrasons
DE4343832A1 (de) *	1993-12-22	1995-06-29	Bayer Ag	Substituierte 1-Arylpyrazole
DE19511269A1 (de) *	1994-03-30	1995-10-05	Ciba Geigy Ag	Pyrazole
DE4414333A1 (de) *	1994-04-25	1995-10-26	Bayer Ag	Substituierte Pyridylpyrazole
WO1996024589A1 (fr) *	1995-02-07	1996-08-15	Nissan Chemical Industries, Ltd.	Derives et herbicides a base de pyrazole
DE19518054A1 (de) *	1995-03-08	1996-09-12	Hoechst Schering Agrevo Gmbh	N-Arylpyrazolketone und deren Derivate, Verfahren zu ihrer Herstellung, sie enthaltende Mittel und ihre Verwendung als Schädlingsbekämpfungsmittel
ATE236883T1 (de) *	1995-12-19	2003-04-15	Bayer Cropscience Sa	Neue 1-aryl pyrazol derivate und ihre verwendung als schädlingsbekämpfungsmittel
AP1237A (en)	1996-12-24	2004-01-14	Merial Ltd	Pesticidal 1-arylpyrazoles.

1997
- 1997-12-18 AP APAP/P/1999/001588A patent/AP1237A/en active
- 1997-12-18 JP JP52835098A patent/JP2001506664A/ja active Pending
- 1997-12-18 BR BR9714181-0A patent/BR9714181A/pt not_active Application Discontinuation
- 1997-12-18 DE DE69738328T patent/DE69738328T2/de not_active Expired - Lifetime
- 1997-12-18 EA EA199900592A patent/EA002085B1/ru not_active IP Right Cessation
- 1997-12-18 EP EP97954422A patent/EP0948486B1/fr not_active Expired - Lifetime
- 1997-12-18 EE EEP199900321A patent/EE05495B1/xx unknown
- 1997-12-18 RS YUP-295/99A patent/RS49966B/sr unknown
- 1997-12-18 SK SK857-99A patent/SK285866B6/sk not_active IP Right Cessation
- 1997-12-18 PT PT97954422T patent/PT948486E/pt unknown
- 1997-12-18 CA CA002275635A patent/CA2275635C/fr not_active Expired - Lifetime
- 1997-12-18 ES ES97954422T patent/ES2297867T3/es not_active Expired - Lifetime
- 1997-12-18 TR TR1999/01473T patent/TR199901473T2/xx unknown
- 1997-12-18 DK DK97954422T patent/DK0948486T3/da active
- 1997-12-18 HU HU0000583A patent/HU229905B1/hu unknown
- 1997-12-18 WO PCT/EP1997/007115 patent/WO1998028277A1/fr not_active Ceased
- 1997-12-18 PL PL334236A patent/PL193231B1/pl unknown
- 1997-12-18 CN CN97180938A patent/CN1099415C/zh not_active Expired - Lifetime
- 1997-12-18 AU AU58575/98A patent/AU746514B2/en not_active Expired
- 1997-12-18 CZ CZ19992298A patent/CZ294766B6/cs not_active IP Right Cessation
- 1997-12-18 KR KR1019997005758A patent/KR20000062319A/ko not_active Abandoned
- 1997-12-18 IL IL13053397A patent/IL130533A/xx not_active IP Right Cessation
- 1997-12-18 NZ NZ336418A patent/NZ336418A/en not_active IP Right Cessation
- 1997-12-22 HR HR970703A patent/HRP970703B1/xx not_active IP Right Cessation
- 1997-12-23 CO CO97074746A patent/CO5031287A1/es unknown
- 1997-12-23 MY MYPI97006260A patent/MY128485A/en unknown
- 1997-12-23 ZA ZA9711590A patent/ZA9711590B/xx unknown
- 1997-12-23 AR ARP970106146A patent/AR011048A1/es unknown
- 1997-12-23 MA MA24912A patent/MA24432A1/fr unknown
- 1997-12-24 ID IDP973973A patent/ID19248A/id unknown
- 1997-12-24 EG EG139097A patent/EG21715A/xx active
1998
- 1998-03-02 TW TW086119718A patent/TW505503B/zh not_active IP Right Cessation
1999
- 1999-06-22 NO NO19993107A patent/NO313458B1/no not_active IP Right Cessation
- 1999-06-22 CU CU1999080A patent/CU22869A3/es unknown
- 1999-06-24 OA OA9900142A patent/OA11133A/en unknown
- 1999-06-24 US US09/339,175 patent/US6087387A/en not_active Expired - Lifetime
- 1999-07-19 BG BG103590A patent/BG64857B1/bg unknown
2000
- 2000-05-26 US US09/578,859 patent/US6403628B1/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
AP9901588A0 (en)	1999-06-30
BG64857B1 (bg)	2006-07-31
BR9714181A (pt)	2000-02-29
CZ229899A3 (cs)	1999-09-15
CA2275635C (fr)	2008-11-25
TW505503B (en)	2002-10-11
AU746514B2 (en)	2002-05-02
DK0948486T3 (da)	2008-03-03
JP2001506664A (ja)	2001-05-22
HU229905B1 (en)	2014-12-29
PL193231B1 (pl)	2007-01-31
NO993107D0 (no)	1999-06-22
ES2297867T3 (es)	2008-05-01
YU29599A (sh)	2001-12-26
CA2275635A1 (fr)	1998-07-02
NZ336418A (en)	2001-06-29
US6087387A (en)	2000-07-11
ID19248A (id)	1998-06-28
AP1237A (en)	2004-01-14
AR011048A1 (es)	2000-08-02
CU22869A3 (es)	2003-09-18
EA199900592A1 (ru)	1999-12-29
CZ294766B6 (cs)	2005-03-16
DE69738328D1 (de)	2008-01-10
MY128485A (en)	2007-02-28
HRP970703B1 (en)	2008-06-30
PL334236A1 (en)	2000-02-14
TR199901473T2 (xx)	1999-10-21
MA24432A1 (fr)	1998-07-01
IL130533A (en)	2005-11-20
EE05495B1 (et)	2011-12-15
EP0948486A1 (fr)	1999-10-13
ZA9711590B (en)	1998-06-25
US6403628B1 (en)	2002-06-11
EE9900321A (et)	2000-06-15
SK85799A3 (en)	2000-01-18
CN1242002A (zh)	2000-01-19
BG103590A (en)	2000-11-30
RS49966B (sr)	2008-09-29
HK1024476A1 (en)	2000-10-13
OA11133A (en)	2003-04-25
PT948486E (pt)	2008-01-21
DE69738328T2 (de)	2008-11-27
HRP970703A2 (en)	1998-10-31
EP0948486B1 (fr)	2007-11-28
WO1998028277A1 (fr)	1998-07-02
HUP0000583A2 (hu)	2000-06-28
NO993107L (no)	1999-08-24
CO5031287A1 (es)	2001-04-27
SK285866B6 (sk)	2007-10-04
EG21715A (en)	2002-02-27
CN1099415C (zh)	2003-01-22
KR20000062319A (ko)	2000-10-25
AU5857598A (en)	1998-07-17
IL130533A0 (en)	2000-06-01
HUP0000583A3 (en)	2001-08-28
EA002085B1 (ru)	2001-12-24

Legal Events

Date	Code	Title	Description
2018-01-08	MK1K	Patent expired

Publication	Publication Date	Title
NO313458B1 (no)	2002-10-07	Pesticide blanding, forbindelse og fremgangsmåte for å kontrollere insekter
AP1004A (en)	2001-08-28	Pesticidal 1-aryl and pyridylpyrazole derivatives.
AP831A (en)	2000-05-03	Novel 5-amino-3-cyano-4-ethysulfinyl-1-pyrazole compounds and their use as pesticides.
BG64557B1 (bg)	2005-07-29	Пестицидни 1-арилпиразоли
CZ95690A3 (cs)	1999-07-14	3-Kyan-1-arylpyrazoly, prostředky, které je obsahují, způsob potírání členovců, nematodů, helminthů a prvoků za jejich použití a meziprodukty k jejich přípravě
NO313828B1 (no)	2002-12-09	Pesticide 1-aryl-3-iminopyrazoler og fremgangsmÕter for fremstilling derav, preparat omfattende slike forbindelser, samtfremgangsmÕte for Õ kontrollere skadedyr
JP4864269B2 (ja)	2012-02-01	農薬としての３−チオメチルピラゾール
EP0973747B1 (fr)	2003-10-15	1-arylpyrazoles pesticides
US20020016468A1 (en)	2002-02-07	Pesticidal 1-arylpyrazole derivatives
MXPA99005968A (en)	2000-01-01	Pesticidal 1-arylpyrazoles
MXPA99005963A (en)	2000-01-01	Pesticidal 1-aryl and pyridylpyrazole derivatives
MXPA99006001A (en)	2000-02-02	Pesticidal 1-arylpyrazoles
CZ296158B6 (cs)	2006-01-11	1-Arylpyrazoly, zpusob jejich prípravy a pesticidní kompozice s jejich obsahem