UA80538C2 - Crystalline hydrates of aryl carboxylic anilide derivatives, a method for preparation thereof (variants), suspended concentrate, multiphase emulsion and a method for controlling plant pathogenic fungi, insects or ticks and regulation of plants growth - Google Patents
Crystalline hydrates of aryl carboxylic anilide derivatives, a method for preparation thereof (variants), suspended concentrate, multiphase emulsion and a method for controlling plant pathogenic fungi, insects or ticks and regulation of plants growth Download PDFInfo
- Publication number
- UA80538C2 UA80538C2 UA20040403075A UA20040403075A UA80538C2 UA 80538 C2 UA80538 C2 UA 80538C2 UA 20040403075 A UA20040403075 A UA 20040403075A UA 20040403075 A UA20040403075 A UA 20040403075A UA 80538 C2 UA80538 C2 UA 80538C2
- Authority
- UA
- Ukraine
- Prior art keywords
- suspended
- hydrate
- insects
- chloro
- ticks
- Prior art date
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- 150000004677 hydrates Chemical class 0.000 title abstract description 9
- 241000238631 Hexapoda Species 0.000 title abstract description 7
- 238000000034 method Methods 0.000 title description 40
- 239000012141 concentrate Substances 0.000 title description 23
- 238000002360 preparation method Methods 0.000 title description 7
- 150000003931 anilides Chemical class 0.000 title description 5
- 239000000839 emulsion Substances 0.000 title description 5
- 241000238876 Acari Species 0.000 title description 4
- 230000033228 biological regulation Effects 0.000 title description 3
- 230000012010 growth Effects 0.000 title description 2
- 125000003118 aryl group Chemical group 0.000 title 1
- 244000000004 fungal plant pathogen Species 0.000 title 1
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- 230000003032 phytopathogenic effect Effects 0.000 abstract description 7
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- 230000008635 plant growth Effects 0.000 abstract description 3
- 238000004519 manufacturing process Methods 0.000 abstract description 2
- ZVSKZLHKADLHSD-UHFFFAOYSA-N benzanilide Chemical class C=1C=CC=CC=1C(=O)NC1=CC=CC=C1 ZVSKZLHKADLHSD-UHFFFAOYSA-N 0.000 abstract 1
- 239000000203 mixture Substances 0.000 description 51
- -1 anilide derivatives of nicotinic acid Chemical class 0.000 description 48
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- 230000000704 physical effect Effects 0.000 description 1
- KNCYXPMJDCCGSJ-UHFFFAOYSA-N piperidine-2,6-dione Chemical compound O=C1CCCC(=O)N1 KNCYXPMJDCCGSJ-UHFFFAOYSA-N 0.000 description 1
- 239000005648 plant growth regulator Substances 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920005646 polycarboxylate Polymers 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 238000000634 powder X-ray diffraction Methods 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 238000004321 preservation Methods 0.000 description 1
- QYMMJNLHFKGANY-UHFFFAOYSA-N profenofos Chemical compound CCCSP(=O)(OCC)OC1=CC=C(Br)C=C1Cl QYMMJNLHFKGANY-UHFFFAOYSA-N 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 229940090181 propyl acetate Drugs 0.000 description 1
- 125000002568 propynyl group Chemical group [*]C#CC([H])([H])[H] 0.000 description 1
- 238000005086 pumping Methods 0.000 description 1
- ROVGZAWFACYCSP-VUMXUWRFSA-N pyrethrin I Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 ROVGZAWFACYCSP-VUMXUWRFSA-N 0.000 description 1
- VJFUPGQZSXIULQ-XIGJTORUSA-N pyrethrin II Chemical compound CC1(C)[C@H](/C=C(\C)C(=O)OC)[C@H]1C(=O)O[C@@H]1C(C)=C(C\C=C/C=C)C(=O)C1 VJFUPGQZSXIULQ-XIGJTORUSA-N 0.000 description 1
- SHNUBALDGXWUJI-UHFFFAOYSA-N pyridin-2-ylmethanol Chemical compound OCC1=CC=CC=N1 SHNUBALDGXWUJI-UHFFFAOYSA-N 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 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
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- ALZOLUNSQWINIR-UHFFFAOYSA-N quinmerac Chemical compound OC(=O)C1=C(Cl)C=CC2=CC(C)=CN=C21 ALZOLUNSQWINIR-UHFFFAOYSA-N 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 230000026267 regulation of growth Effects 0.000 description 1
- 239000013049 sediment Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- HPYNBECUCCGGPA-UHFFFAOYSA-N silafluofen Chemical compound C1=CC(OCC)=CC=C1[Si](C)(C)CCCC1=CC=C(F)C(OC=2C=CC=CC=2)=C1 HPYNBECUCCGGPA-UHFFFAOYSA-N 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 238000010583 slow cooling Methods 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 235000021012 strawberries Nutrition 0.000 description 1
- 150000003871 sulfonates Chemical class 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
- 238000003786 synthesis reaction Methods 0.000 description 1
- 239000005936 tau-Fluvalinate Substances 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 230000009974 thixotropic effect Effects 0.000 description 1
- YWSCPYYRJXKUDB-KAKFPZCNSA-N tralomethrin Chemical compound CC1(C)[C@@H](C(Br)C(Br)(Br)Br)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 YWSCPYYRJXKUDB-KAKFPZCNSA-N 0.000 description 1
- ZOKXUAHZSKEQSS-UHFFFAOYSA-N tribufos Chemical compound CCCCSP(=O)(SCCCC)SCCCC ZOKXUAHZSKEQSS-UHFFFAOYSA-N 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- NQPDZGIKBAWPEJ-UHFFFAOYSA-N valeric acid Chemical compound CCCCC(O)=O NQPDZGIKBAWPEJ-UHFFFAOYSA-N 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- MAZZTUAWFTWGKB-UHFFFAOYSA-L zinc ethane-1,2-diamine manganese(2+) dicarbamodithioate Chemical compound [Mn+2].[Zn+2].NCCN.NC([S-])=S.NC([S-])=S MAZZTUAWFTWGKB-UHFFFAOYSA-L 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- 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
- A01N43/34—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom
- A01N43/40—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one nitrogen atom as the only ring hetero atom six-membered rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C233/00—Carboxylic acid amides
- C07C233/64—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings
- C07C233/66—Carboxylic acid amides having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings having the nitrogen atom of at least one of the carboxamide groups bound to a carbon atom of a hydrocarbon radical substituted by halogen atoms or by nitro or nitroso groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
- C07D213/82—Amides; Imides in position 3
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Dentistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Plant Pathology (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pyridine Compounds (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10147034 | 2001-09-25 | ||
| PCT/EP2002/010320 WO2003029219A1 (de) | 2001-09-25 | 2002-09-14 | Kristalline hydrate von nicotinsaeurenilid- und benzoylanilid-derivaten |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| UA80538C2 true UA80538C2 (en) | 2007-10-10 |
Family
ID=7700100
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| UA20040403075A UA80538C2 (en) | 2001-09-25 | 2002-09-14 | Crystalline hydrates of aryl carboxylic anilide derivatives, a method for preparation thereof (variants), suspended concentrate, multiphase emulsion and a method for controlling plant pathogenic fungi, insects or ticks and regulation of plants growth |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US7087239B2 (es) |
| EP (1) | EP1432685B1 (es) |
| JP (1) | JP4401773B2 (es) |
| KR (2) | KR20090127446A (es) |
| CN (1) | CN1275943C (es) |
| AR (1) | AR036578A1 (es) |
| AT (1) | ATE290530T1 (es) |
| AU (1) | AU2002338695B2 (es) |
| BR (1) | BR0212685A (es) |
| CA (1) | CA2460654C (es) |
| CO (1) | CO5560606A2 (es) |
| DE (1) | DE50202440D1 (es) |
| DK (1) | DK1432685T3 (es) |
| EA (1) | EA007780B1 (es) |
| ES (1) | ES2238610T3 (es) |
| HU (1) | HUP0402129A3 (es) |
| IL (2) | IL160640A0 (es) |
| MX (1) | MXPA04002036A (es) |
| MY (1) | MY131952A (es) |
| NZ (1) | NZ531778A (es) |
| PL (1) | PL220091B1 (es) |
| PT (1) | PT1432685E (es) |
| SI (1) | SI1432685T1 (es) |
| TW (1) | TWI281469B (es) |
| UA (1) | UA80538C2 (es) |
| WO (1) | WO2003029219A1 (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10307751A1 (de) | 2003-02-14 | 2004-08-26 | Basf Ag | Neue kristalline Modifikation des Anhydrates von Boscalid |
| EP1659864B1 (en) * | 2003-08-26 | 2013-09-18 | Basf Se | Method of plant growth promotion using amide compounds |
| WO2006137389A1 (ja) * | 2005-06-21 | 2006-12-28 | Meiji Seika Kaisha Ltd. | 新規殺虫、殺ダニ剤 |
| UA90035C2 (ru) | 2005-11-10 | 2010-03-25 | Басф Се | Фунгицидная смесь, которая содержит боскалид и пириметанил и способ борьбы с фитопатогенными грибами |
| MX2009003431A (es) * | 2006-10-13 | 2009-04-14 | Basf Se | Hidratos de 2-cloro-5-[3,6-dihidro-3-metil-2,6-dioxo-4-(trifluorom etil)-1-(2h)-pirimidinil]-4-fluor-n-[[metil(1-metiletil)amino]sul fonil]benzamida. |
| MX2009003497A (es) * | 2006-10-13 | 2009-04-14 | Basf Se | Forma cristalina de 2-cloro-5-[3,6-dihidro-3-metil-2,6-dioxo-4-(tr ifluorometil)-1-(2h)-pirimidinil]-4-fluoro-n-[[metil(1-metiletil) amino]sulfonil]benzamida. |
| JP5422560B2 (ja) * | 2007-08-09 | 2014-02-19 | ビーエーエスエフ ソシエタス・ヨーロピア | 殺菌剤混合物 |
| US20090280983A1 (en) * | 2008-05-08 | 2009-11-12 | Rui Luiz Correa Picanco | Fertilizer - pesticide throw-pack |
| JP2013537169A (ja) | 2010-09-09 | 2013-09-30 | サンコー・エナジー・インコーポレーテッド | 相乗作用を有するパラフィン系オイルおよびボスカリド殺菌剤 |
| CN103348982B (zh) | 2013-07-15 | 2016-06-15 | 江苏龙灯化学有限公司 | 一种杀真菌混合物 |
| CN103980192B (zh) * | 2014-01-20 | 2016-02-17 | 泰州百力化学股份有限公司 | 一种选择性合成不同晶型啶酰菌胺的方法 |
| GB2539022B (en) * | 2015-06-04 | 2018-02-07 | Rotam Agrochem Int Co Ltd | Process for preparing boscalid |
| GB2536979B (en) * | 2015-06-04 | 2019-03-13 | Rotam Agrochem Int Co Ltd | Process for preparing boscalid |
| GB2550138B (en) * | 2016-05-09 | 2019-06-12 | Rotam Agrochem Int Co Ltd | Process for preparing boscalid |
| GB2552699B (en) * | 2016-08-04 | 2021-03-10 | Rotam Agrochem Int Co Ltd | Process for preparing boscalid |
| GB2552696B (en) * | 2016-08-04 | 2020-03-04 | Rotam Agrochem Int Co Ltd | Process for preparing boscalid |
| GB2552697B (en) * | 2016-08-04 | 2021-03-10 | Rotam Agrochem Int Co Ltd | Process for the preparation of boscalid |
| CN106083712B (zh) * | 2016-08-23 | 2018-10-16 | 王正友 | 一种烟酰苯胺盐的合成方法 |
| WO2018060836A1 (en) | 2016-09-28 | 2018-04-05 | Upl Limited | Process for preparation of boscalid anhydrate form i and boscalid anhydrate form ii |
| CN114181141A (zh) * | 2021-12-09 | 2022-03-15 | 江阴苏利化学股份有限公司 | 一种啶酰菌胺晶型ⅰ的制备方法 |
| CN115536581A (zh) * | 2022-10-08 | 2022-12-30 | 河北兰升生物科技有限公司 | 高纯度啶酰菌胺晶型i的制备方法 |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2081935C (en) * | 1991-11-22 | 2004-05-25 | Karl Eicken | Anilide derivatives and their use for combating botrytis |
| DE4231517A1 (de) | 1992-09-21 | 1994-03-24 | Basf Ag | Carbonsäureanilide, Verfahren zu ihrer Herstellung und sie enthaltende Mittel zur Bekämpfung von Schadpilzen |
| DE4322211A1 (de) | 1993-07-03 | 1995-01-12 | Basf Ag | Wäßrige, mehrphasige, stabile Fertigformulierung für Pflanzenschutz-Wirkstoffe und Verfahren zu ihrer Herstellung |
| DE4331416A1 (de) * | 1993-12-09 | 1995-06-14 | Bayer Ag | Verwendung von Phenylcarbonsäure-amiden als Kristallisationsinhibitoren |
| TW431861B (en) * | 1997-12-18 | 2001-05-01 | Basf Ag | Fungicidal mixtures based on amide compounds and azoles |
| AU2003210237A1 (en) * | 2002-02-23 | 2003-09-09 | Bayer Cropscience Aktiengesellschaft | Microbicidal agents on the basis of biphenyl benzamide derivatives |
-
2002
- 2002-09-14 US US10/490,370 patent/US7087239B2/en not_active Expired - Lifetime
- 2002-09-14 IL IL16064002A patent/IL160640A0/xx unknown
- 2002-09-14 HU HU0402129A patent/HUP0402129A3/hu unknown
- 2002-09-14 UA UA20040403075A patent/UA80538C2/uk unknown
- 2002-09-14 CA CA2460654A patent/CA2460654C/en not_active Expired - Lifetime
- 2002-09-14 KR KR1020097024656A patent/KR20090127446A/ko not_active Application Discontinuation
- 2002-09-14 WO PCT/EP2002/010320 patent/WO2003029219A1/de active Application Filing
- 2002-09-14 JP JP2003532469A patent/JP4401773B2/ja not_active Expired - Fee Related
- 2002-09-14 PT PT02777103T patent/PT1432685E/pt unknown
- 2002-09-14 KR KR1020047004263A patent/KR100949627B1/ko active IP Right Grant
- 2002-09-14 CN CNB028187539A patent/CN1275943C/zh not_active Expired - Fee Related
- 2002-09-14 BR BR0212685-0A patent/BR0212685A/pt not_active Application Discontinuation
- 2002-09-14 NZ NZ531778A patent/NZ531778A/en not_active IP Right Cessation
- 2002-09-14 DE DE50202440T patent/DE50202440D1/de not_active Expired - Lifetime
- 2002-09-14 EA EA200400414A patent/EA007780B1/ru not_active IP Right Cessation
- 2002-09-14 PL PL370406A patent/PL220091B1/pl unknown
- 2002-09-14 AT AT02777103T patent/ATE290530T1/de active
- 2002-09-14 MX MXPA04002036A patent/MXPA04002036A/es active IP Right Grant
- 2002-09-14 EP EP02777103A patent/EP1432685B1/de not_active Expired - Lifetime
- 2002-09-14 AU AU2002338695A patent/AU2002338695B2/en not_active Ceased
- 2002-09-14 DK DK02777103T patent/DK1432685T3/da active
- 2002-09-14 SI SI200230123T patent/SI1432685T1/xx unknown
- 2002-09-14 ES ES02777103T patent/ES2238610T3/es not_active Expired - Lifetime
- 2002-09-25 MY MYPI20023580A patent/MY131952A/en unknown
- 2002-09-25 AR ARP020103603A patent/AR036578A1/es unknown
- 2002-09-25 TW TW091122015A patent/TWI281469B/zh not_active IP Right Cessation
-
2004
- 2004-02-26 IL IL160640A patent/IL160640A/en not_active IP Right Cessation
- 2004-03-24 CO CO04027791A patent/CO5560606A2/es not_active Application Discontinuation
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