UA77411C2 - Parasiticide agent for the dermal application on animals - Google Patents
Parasiticide agent for the dermal application on animals Download PDFInfo
- Publication number
- UA77411C2 UA77411C2 UA20031110065A UA20031110065A UA77411C2 UA 77411 C2 UA77411 C2 UA 77411C2 UA 20031110065 A UA20031110065 A UA 20031110065A UA 20031110065 A UA20031110065 A UA 20031110065A UA 77411 C2 UA77411 C2 UA 77411C2
- Authority
- UA
- Ukraine
- Prior art keywords
- permethrin
- ticks
- animals
- methyl
- imidacloprid
- Prior art date
Links
- 230000036576 dermal application Effects 0.000 title abstract description 3
- 241001465754 Metazoa Species 0.000 title description 26
- 239000003795 chemical substances by application Substances 0.000 title description 2
- 230000000590 parasiticidal effect Effects 0.000 title 1
- 239000002297 parasiticide Substances 0.000 title 1
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- 239000000203 mixture Substances 0.000 abstract description 26
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- 239000005906 Imidacloprid Substances 0.000 abstract description 20
- YWTYJOPNNQFBPC-UHFFFAOYSA-N imidacloprid Chemical compound [O-][N+](=O)\N=C1/NCCN1CC1=CC=C(Cl)N=C1 YWTYJOPNNQFBPC-UHFFFAOYSA-N 0.000 abstract description 20
- 229940056881 imidacloprid Drugs 0.000 abstract description 20
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- 238000009472 formulation Methods 0.000 abstract 1
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- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003222 pyridines Chemical class 0.000 description 1
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229940125723 sedative agent Drugs 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 125000000475 sulfinyl group Chemical group [*:2]S([*:1])=O 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000000335 thiazolyl group Chemical group 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 description 1
- 229960004175 xylazine hydrochloride Drugs 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical & Material Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Zoology (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Tropical Medicine & Parasitology (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicinal Preparation (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Thiazole And Isothizaole Compounds (AREA)
- Pyridine Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10117676A DE10117676A1 (de) | 2001-04-09 | 2001-04-09 | Dermal applizierbare flüssige Formulierungen zur Bekämpfung von parasitierenden Insekten an Tieren |
PCT/EP2002/003619 WO2002087338A1 (fr) | 2001-04-09 | 2002-04-02 | Formulations liquides a application cutanee pour lutter contre des insectes parasites sur des animaux |
Publications (1)
Publication Number | Publication Date |
---|---|
UA77411C2 true UA77411C2 (en) | 2006-12-15 |
Family
ID=7680960
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UA20031110065A UA77411C2 (en) | 2001-04-09 | 2002-02-04 | Parasiticide agent for the dermal application on animals |
Country Status (29)
Country | Link |
---|---|
US (1) | US7728011B2 (fr) |
EP (1) | EP1379138B1 (fr) |
JP (2) | JP4767478B2 (fr) |
KR (1) | KR100883848B1 (fr) |
CN (2) | CN101036648A (fr) |
AT (1) | ATE309702T1 (fr) |
AU (1) | AU2002338488B2 (fr) |
BR (1) | BR0208733B1 (fr) |
CA (1) | CA2443159C (fr) |
CO (1) | CO5540359A2 (fr) |
CR (1) | CR7089A (fr) |
CZ (1) | CZ302251B6 (fr) |
DE (2) | DE10117676A1 (fr) |
DK (1) | DK1379138T3 (fr) |
EE (1) | EE05477B1 (fr) |
ES (1) | ES2250701T3 (fr) |
HK (1) | HK1066449A1 (fr) |
HR (1) | HRP20030904B1 (fr) |
HU (1) | HU229934B1 (fr) |
IL (2) | IL158068A0 (fr) |
MX (1) | MXPA03009134A (fr) |
NO (1) | NO330537B1 (fr) |
NZ (1) | NZ528664A (fr) |
PL (1) | PL205958B1 (fr) |
RU (1) | RU2296466C2 (fr) |
SK (1) | SK286434B6 (fr) |
UA (1) | UA77411C2 (fr) |
WO (1) | WO2002087338A1 (fr) |
ZA (1) | ZA200307816B (fr) |
Families Citing this family (33)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE4417742A1 (de) | 1994-05-20 | 1995-11-23 | Bayer Ag | Nicht-systemische Bekämpfung von Parasiten |
US20020103233A1 (en) * | 2000-11-30 | 2002-08-01 | Arther Robert G. | Compositions for enhanced acaricidal activity |
DE10301906A1 (de) * | 2003-01-17 | 2004-07-29 | Bayer Healthcare Ag | Repellentmittel |
DE10320505A1 (de) * | 2003-05-08 | 2004-11-25 | Bayer Healthcare Ag | Mittel zum Bekämpfen von Parasiten an Tieren |
DE10337305A1 (de) * | 2003-07-02 | 2005-02-03 | Andresen, Uwe, Prof. Dr. | Parasitizide, repellierende Zusammensetzung und Verfahren zu ihrer Herstellung und ihrer Verwendung |
US7901700B2 (en) | 2004-01-09 | 2011-03-08 | Fmc Corporation | Bifenthrin/acetamiprid compositions for control of general household pests |
CN100525625C (zh) | 2004-01-09 | 2009-08-12 | Fmc有限公司 | 用于控制常见家庭害虫的杀虫组合物 |
DE102004006324A1 (de) * | 2004-02-10 | 2005-08-25 | Bayer Cropscience Ag | Wirkstoffkombinationen mit insektiziden Eigenschaften |
CN100525626C (zh) | 2004-03-25 | 2009-08-12 | Fmc有限公司 | 拟除虫菊酯和灭虫碱的液体杀白蚁剂组合物 |
DE102004020721A1 (de) * | 2004-04-28 | 2005-11-24 | Bayer Healthcare Ag | Dermal applizierbare flüssige Formulierungen zur Bekämpfung von parasitierenden Insekten an Tieren |
DE102004053964A1 (de) | 2004-11-09 | 2006-05-11 | Bayer Healthcare Ag | Mittel gegen Demodikose |
US7704955B2 (en) * | 2004-11-24 | 2010-04-27 | Neopro Pain, Inc. | Methods and compositions for modulating conditions in both mammals and plants |
FR2880269B1 (fr) * | 2004-12-31 | 2008-11-07 | Cardon Pharmaceuticals Nv Sa | Produit traitant pour animaux et moyens pour sa preparation |
ITMI20061825A1 (it) * | 2006-09-26 | 2008-03-27 | Giuliani Spa | Composizione antipediculosi provvista di attivita' di soffocamento dei pidocchi |
TW200846029A (en) * | 2007-02-09 | 2008-12-01 | Wyeth Corp | High dose, long-acting ectoparasiticide for extended control |
DE102007025609A1 (de) * | 2007-05-31 | 2008-12-11 | Meyer, Ulrich, Dr. | Mittel zur Zeckenentfernung |
US8404260B2 (en) | 2008-04-02 | 2013-03-26 | Bayer Cropscience Lp | Synergistic pesticide compositions |
CH702717A2 (de) | 2010-02-26 | 2011-08-31 | Solnova Ag | Spot-on-Präparat. |
UA108641C2 (uk) | 2010-04-02 | 2015-05-25 | Паразитицидна композиція, яка містить чотири активних агенти, та спосіб її застосування | |
JO3626B1 (ar) * | 2012-02-23 | 2020-08-27 | Merial Inc | تركيبات موضعية تحتوي على فيبرونيل و بيرميثرين و طرق استخدامها |
DE202012004045U1 (de) | 2012-04-16 | 2012-05-02 | Solnova Ag | Spot-on-Präparat |
EA028544B1 (ru) * | 2013-02-27 | 2017-11-30 | КРКА, д.д., НОВО МЕСТО | Ветеринарная композиция для борьбы с паразитами для накожного применения и ее применение |
WO2015007923A1 (fr) * | 2013-07-18 | 2015-01-22 | König Lab, S.L. | Procédé de déparasitage d'animaux par application simultanée d'au moins deux agents parasiticides par voie dermique et dispositif pour sa mise en pratique |
US10721930B2 (en) | 2014-12-23 | 2020-07-28 | Cap Innovet, Inc. | Dermal compositions |
EP3324736B1 (fr) | 2015-07-17 | 2019-04-10 | Evergreen Animal Health LLC | Nouvelle formulation de principes actifs localisés |
CN105567105B (zh) * | 2015-12-30 | 2018-03-16 | 天津德高化成光电科技有限责任公司 | 高折射率芯片级封装led白光芯片荧光胶膜及制备方法 |
ES2792056T3 (es) | 2017-01-17 | 2020-11-06 | Evergreen Animal Health Llc | Novedosa formulación de un principio activo para unción puntual |
US10172359B2 (en) * | 2017-05-17 | 2019-01-08 | Sergeant's Pet Care Products, Inc. | Solvent system for use with spot-on pesticide compositions |
US11344532B2 (en) * | 2017-09-06 | 2022-05-31 | Bayer Animal Health Gmbh | Topically administrable formulation for the control and prevention of animal parasites |
WO2020150032A1 (fr) | 2019-01-16 | 2020-07-23 | Boehringer Ingelheim Animal Health USA Inc. | Compositions topiques comprenant un néonicotinoïde et une lactone macrocyclique, procédés et utilisations associés |
EP3771335A1 (fr) | 2019-07-31 | 2021-02-03 | Athenion AG | Composition répulsive |
PL435706A1 (pl) * | 2020-10-16 | 2022-04-19 | Tg Pharma Spółka Z Ograniczoną Odpowiedzialnością | Permetryna do zastosowania w leczeniu zewnętrznym infestacji Demodex spp. |
CN113616653A (zh) * | 2021-09-04 | 2021-11-09 | 浙江海正动物保健品有限公司 | 一种低温稳定性好的含吡虫啉的复方制剂及其制备方法 |
Family Cites Families (68)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB8323061D0 (en) | 1983-08-26 | 1983-09-28 | Shell Int Research | Pesticidal heterocyclic compounds |
JPH0629256B2 (ja) * | 1983-10-06 | 1994-04-20 | 日本バイエルアグロケム株式会社 | ニトロメチレン−テトラヒドロピリミジン誘導体,その製法及び殺虫,殺ダニ,殺センチユウ剤 |
JPS60172976A (ja) * | 1984-02-16 | 1985-09-06 | Nippon Tokushu Noyaku Seizo Kk | ニトロメチレン誘導体,その製法及び殺虫,殺ダニ,殺センチユウ剤 |
ZW5085A1 (en) * | 1984-04-13 | 1985-09-18 | Nihon Tokushu Noyaku Seizo Kk | Nitromethylene derivatives,intermediates thereof,processes for production thereof,and insecticides |
GB8500863D0 (en) | 1985-01-14 | 1985-02-20 | Fine Organics Ltd | Preparation of thiazine derivatives |
DE3681465D1 (fr) * | 1985-02-04 | 1991-10-24 | Nihon Bayer Agrochem K.K., Tokio/Tokyo, Jp | |
JPH072736B2 (ja) * | 1985-08-27 | 1995-01-18 | 日本バイエルアグロケム株式会社 | ニトロメチレン誘導体、その製法及び殺虫剤 |
JPH0717621B2 (ja) * | 1986-03-07 | 1995-03-01 | 日本バイエルアグロケム株式会社 | 新規ヘテロ環式化合物 |
JPH085859B2 (ja) * | 1986-07-01 | 1996-01-24 | 日本バイエルアグロケム株式会社 | 新規アルキレンジアミン類 |
JPH07121909B2 (ja) * | 1986-09-10 | 1995-12-25 | 日本バイエルアグロケム株式会社 | 新規複素環式化合物及び殺虫剤 |
DE3634755A1 (de) * | 1986-10-11 | 1988-04-14 | Bayer Ag | Dermale behandlung von wurmerkrankungen der katze mit praziquantel |
DE3639877A1 (de) | 1986-11-21 | 1988-05-26 | Bayer Ag | Hetarylalkyl substituierte 5- und 6-ringheterocyclen |
US4963574A (en) * | 1987-02-24 | 1990-10-16 | Ciba-Geigy Corporation | N-cyanoisothiourea compounds useful in pest control |
DE3712307A1 (de) | 1987-04-10 | 1988-10-20 | Bayer Ag | 3-substituierte 1-(2-chlor-thiazol-5-yl-methyl)-2- nitroimino-1,3-diazacycloalkane |
JPS63287764A (ja) | 1987-05-21 | 1988-11-24 | Nippon Tokushu Noyaku Seizo Kk | N−3−シアノベンジル−ヘテロ環式化合物及び殺虫剤 |
JP2597095B2 (ja) | 1987-06-09 | 1997-04-02 | 日本バイエルアグロケム株式会社 | シアノアルキル―ヘテロ環式化合物を含有する殺虫剤 |
CH673557A5 (fr) * | 1987-07-20 | 1990-03-30 | Ciba Geigy Ag | |
DE3856183T2 (de) | 1987-08-01 | 1998-11-05 | Takeda Chemical Industries Ltd | Zwischenprodukte, ihre Herstellung und Verwendung zur Herstellung alpha-ungesättigter Amine |
EP0306696B1 (fr) * | 1987-08-04 | 1994-02-16 | Ciba-Geigy Ag | Guanidines substituées |
US4918086A (en) * | 1987-08-07 | 1990-04-17 | Ciba-Geigy Corporation | 1-nitro-2,2-diaminoethylene derivatives |
EP0303570A3 (fr) * | 1987-08-12 | 1990-11-07 | Ciba-Geigy Ag | Isothiourées substituées |
JP2583429B2 (ja) * | 1987-11-06 | 1997-02-19 | 日本バイエルアグロケム株式会社 | イミダゾリン類及び殺虫剤 |
US5074252A (en) * | 1988-03-25 | 1991-12-24 | Morgan Jr Charles | Rechargeable insecticide dispenser providing controlled release of an insecticide composition |
JP2884412B2 (ja) | 1988-10-21 | 1999-04-19 | 日本バイエルアグロケム株式会社 | 殺虫性シアノ化合物 |
JPH0699777B2 (ja) | 1988-11-02 | 1994-12-07 | 株式会社東芝 | 低熱膨張鋳鉄の製造方法 |
GB8826539D0 (en) * | 1988-11-14 | 1988-12-21 | Shell Int Research | Nitromethylene compounds their preparation & their use as pesticides |
JP2779403B2 (ja) | 1988-11-29 | 1998-07-23 | 日本バイエルアグロケム株式会社 | 殺虫性ニトロ化合物 |
IE960442L (en) * | 1988-12-27 | 1990-06-27 | Takeda Chemical Industries Ltd | Guanidine derivatives, their production and insecticides |
JP2822050B2 (ja) | 1989-02-04 | 1998-11-05 | 日本バイエルアグロケム株式会社 | 2―ニトロイミノイミダゾリジン類の製法 |
DK0383091T3 (da) | 1989-02-13 | 1994-02-07 | Bayer Agrochem Kk | Insecticidt virksomme nitroforbindelser |
JP2610988B2 (ja) * | 1989-03-09 | 1997-05-14 | 日本バイエルアグロケム 株式会社 | 新規ヘテロ環式化合物及び殺虫剤 |
EP0387663B1 (fr) | 1989-03-17 | 1993-09-01 | Bayer Ag | Agent contre des parasites de la kératine |
JPH03200768A (ja) | 1989-10-24 | 1991-09-02 | Agro Kanesho Co Ltd | ニトログアニジン化合物及び殺虫剤 |
AU628229B2 (en) | 1989-11-10 | 1992-09-10 | Agro-Kanesho Co. Ltd. | Hexahydrotriazine compounds and insecticides |
JP2943246B2 (ja) | 1990-01-11 | 1999-08-30 | 日本曹達株式会社 | ニトロエチレン誘導体、その製造方法及び殺虫剤 |
JP2867345B2 (ja) | 1990-01-23 | 1999-03-08 | 日本バイエルアグロケム株式会社 | 殺虫性トリフルオロアセチル誘導体 |
US5253182A (en) * | 1990-02-20 | 1993-10-12 | Hitachi, Ltd. | Method of and apparatus for converting design pattern data to exposure data |
DE69126776T2 (de) * | 1990-03-05 | 1998-01-08 | Mallinckrodt Veterinary, Inc., Terre Haute, Ind. | Parasitizide zusammensetzung und verfahren zu ihrer herstellung und ihre verwendung |
JPH03279359A (ja) | 1990-03-27 | 1991-12-10 | Ishihara Sangyo Kaisha Ltd | ニトログアニジン誘導体、それらの製造方法及びそれらを含有する有害生物防除剤 |
US5192778A (en) | 1990-04-03 | 1993-03-09 | Mitsui Toatsu Chemicals, Inc. | Dialkoxymethylimidazolidine derivatives, preparation thereof, insecticides containing same as an effective ingredient and intermediates therefor |
JPH05507088A (ja) | 1990-05-17 | 1993-10-14 | ユニバーシテイ・オブ・サウスカロライナ | 殺節足動物性ニトロエチレン及びニトログアニジン |
JP2924102B2 (ja) | 1990-06-15 | 1999-07-26 | 住友化学工業株式会社 | ダニ防除剤 |
JPH0739430B2 (ja) | 1990-07-06 | 1995-05-01 | アグロカネショウ株式会社 | 有機リン化合物、その製造法および該化合物を含有する殺虫、殺ダニ、殺線虫剤 |
IL99161A (en) | 1990-08-17 | 1996-11-14 | Takeda Chemical Industries Ltd | History of guanidine A process for their preparation and preparations from pesticides that contain them |
FR2689729B1 (fr) * | 1992-04-09 | 1994-06-03 | Roussel Uclaf | Nouvelles compositions pesticides renfermant un pyrethrinouide. |
JPH0789803A (ja) | 1993-09-24 | 1995-04-04 | Japan Carlit Co Ltd:The | 無臭性防蟻剤 |
US6267947B1 (en) | 1993-12-23 | 2001-07-31 | Sun Glitz Corporation | Water resistant pesticide composition |
JP3713582B2 (ja) * | 1994-02-27 | 2005-11-09 | 日本農薬株式会社 | 土壌処理用白蟻類防除組成物及び防除方法 |
JPH07247203A (ja) | 1994-03-10 | 1995-09-26 | Osaka Seiyaku:Kk | ノミ防除剤 |
DE4417742A1 (de) * | 1994-05-20 | 1995-11-23 | Bayer Ag | Nicht-systemische Bekämpfung von Parasiten |
JP3493476B2 (ja) * | 1994-09-30 | 2004-02-03 | バイエルクロップサイエンス株式会社 | 白蟻防除剤組成物 |
DE4443888A1 (de) * | 1994-12-09 | 1996-06-13 | Bayer Ag | Dermal applizierbare Formulierungen von Parasitiziden |
DE19654079A1 (de) * | 1996-12-23 | 1998-06-25 | Bayer Ag | Endo-ekto-parasitizide Mittel |
RU2127517C1 (ru) * | 1997-03-11 | 1999-03-20 | Открытое акционерное общество "Арнест" | Инсектицидная композиция |
RU2130259C1 (ru) * | 1997-05-07 | 1999-05-20 | Открытое акционерное общество "Арнест" | Аэрозольное средство для уничтожения моли и кожеедов |
CN1176052A (zh) * | 1997-07-23 | 1998-03-18 | 张天良 | 一种杀虫剂 |
JP3239207B2 (ja) * | 1997-09-05 | 2001-12-17 | 大日本除蟲菊株式会社 | 防蟻・防腐処理剤 |
DE19807633A1 (de) * | 1998-02-23 | 1999-08-26 | Bayer Ag | Dermal applizierbare wasserhaltige Formulierungen von Parasitiziden |
CN1236547A (zh) * | 1998-05-21 | 1999-12-01 | 张天良 | 一种杀虫剂 |
AU744790B2 (en) | 1998-07-27 | 2002-03-07 | Sumitomo Chemical Company, Limited | Ectoparasite controlling agent for animals |
US6033731A (en) * | 1998-08-19 | 2000-03-07 | Nova Chemicals, Inc. | Impregnating polymer beads with insecticide |
US6080796A (en) * | 1998-08-19 | 2000-06-27 | Nova Chemicals Inc. | Dissolving insecticide in monomer |
JP3460590B2 (ja) * | 1998-09-03 | 2003-10-27 | アース製薬株式会社 | 溶解剤及び殺虫液剤 |
FR2784011B1 (fr) * | 1998-10-05 | 2006-08-25 | Rhone Poulenc Agrochimie | Composition insecticide comprenant de la cypermethrine et de l' acetamiprid |
CN1234181A (zh) * | 1999-01-08 | 1999-11-10 | 吕玉成 | 高效氯氰菊脂吡虫啉乳油 |
BR0017605B1 (pt) | 1999-03-12 | 2013-01-22 | composiÇço inseticida sinÉrgica, processo para controle de insetos e processo para proteger plantas contra infestaÇço e ataque de insetos. | |
US6660690B2 (en) * | 2000-10-06 | 2003-12-09 | Monsanto Technology, L.L.C. | Seed treatment with combinations of insecticides |
US20020103233A1 (en) * | 2000-11-30 | 2002-08-01 | Arther Robert G. | Compositions for enhanced acaricidal activity |
-
2001
- 2001-04-09 DE DE10117676A patent/DE10117676A1/de not_active Withdrawn
-
2002
- 2002-02-04 UA UA20031110065A patent/UA77411C2/uk unknown
- 2002-04-02 CN CNA2007100936717A patent/CN101036648A/zh active Pending
- 2002-04-02 IL IL15806802A patent/IL158068A0/xx active IP Right Grant
- 2002-04-02 MX MXPA03009134A patent/MXPA03009134A/es active IP Right Grant
- 2002-04-02 SK SK1235-2003A patent/SK286434B6/sk not_active IP Right Cessation
- 2002-04-02 CA CA2443159A patent/CA2443159C/fr not_active Expired - Lifetime
- 2002-04-02 AU AU2002338488A patent/AU2002338488B2/en not_active Expired
- 2002-04-02 AT AT02766612T patent/ATE309702T1/de active
- 2002-04-02 ES ES02766612T patent/ES2250701T3/es not_active Expired - Lifetime
- 2002-04-02 DE DE50204946T patent/DE50204946D1/de not_active Expired - Lifetime
- 2002-04-02 JP JP2002584703A patent/JP4767478B2/ja not_active Expired - Lifetime
- 2002-04-02 EE EEP200300490A patent/EE05477B1/xx unknown
- 2002-04-02 KR KR1020037012476A patent/KR100883848B1/ko active IP Right Grant
- 2002-04-02 WO PCT/EP2002/003619 patent/WO2002087338A1/fr active IP Right Grant
- 2002-04-02 CN CNB028079345A patent/CN100337545C/zh not_active Expired - Lifetime
- 2002-04-02 CZ CZ20032724A patent/CZ302251B6/cs not_active IP Right Cessation
- 2002-04-02 HU HU0303840A patent/HU229934B1/hu unknown
- 2002-04-02 BR BRPI0208733-2B1A patent/BR0208733B1/pt active IP Right Grant
- 2002-04-02 NZ NZ528664A patent/NZ528664A/en not_active IP Right Cessation
- 2002-04-02 DK DK02766612T patent/DK1379138T3/da active
- 2002-04-02 PL PL367026A patent/PL205958B1/pl unknown
- 2002-04-02 EP EP02766612A patent/EP1379138B1/fr not_active Expired - Lifetime
- 2002-04-02 RU RU2003132544/15A patent/RU2296466C2/ru active
-
2003
- 2003-09-23 IL IL158068A patent/IL158068A/en unknown
- 2003-10-01 CR CR7089A patent/CR7089A/es unknown
- 2003-10-07 ZA ZA200307816A patent/ZA200307816B/en unknown
- 2003-10-08 NO NO20034512A patent/NO330537B1/no not_active IP Right Cessation
- 2003-10-09 US US10/682,127 patent/US7728011B2/en active Active
- 2003-11-07 HR HR20030904A patent/HRP20030904B1/xx not_active IP Right Cessation
- 2003-11-07 CO CO03098927A patent/CO5540359A2/es active IP Right Grant
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2004
- 2004-11-29 HK HK04109399A patent/HK1066449A1/xx not_active IP Right Cessation
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2010
- 2010-01-18 JP JP2010008388A patent/JP2010155844A/ja active Pending
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