CA2857974A1 - Herbicidal composition containing 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or derivative thereof and fluroxypyr or derivatives thereof - Google Patents
Herbicidal composition containing 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or derivative thereof and fluroxypyr or derivatives thereof Download PDFInfo
- Publication number
- CA2857974A1 CA2857974A1 CA2857974A CA2857974A CA2857974A1 CA 2857974 A1 CA2857974 A1 CA 2857974A1 CA 2857974 A CA2857974 A CA 2857974A CA 2857974 A CA2857974 A CA 2857974A CA 2857974 A1 CA2857974 A1 CA 2857974A1
- Authority
- CA
- Canada
- Prior art keywords
- composition
- fluroxypyr
- carboxylic acid
- ester
- salt
- Prior art date
- Legal status (The legal status 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 status listed.)
- Abandoned
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- 239000005558 Fluroxypyr Substances 0.000 title claims abstract description 39
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- 230000002363 herbicidal effect Effects 0.000 title claims abstract description 37
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- ASRAWSBMDXVNLX-UHFFFAOYSA-N pyrazolynate Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OS(=O)(=O)C1=CC=C(C)C=C1 ASRAWSBMDXVNLX-UHFFFAOYSA-N 0.000 description 1
- FKERUJTUOYLBKB-UHFFFAOYSA-N pyrazoxyfen Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(=O)C=1C(C)=NN(C)C=1OCC(=O)C1=CC=CC=C1 FKERUJTUOYLBKB-UHFFFAOYSA-N 0.000 description 1
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- 229910052903 pyrophyllite Inorganic materials 0.000 description 1
- 150000003242 quaternary ammonium salts 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
- 150000003248 quinolines Chemical class 0.000 description 1
- ABOOPXYCKNFDNJ-SNVBAGLBSA-N quizalofop-P Chemical compound C1=CC(O[C@H](C)C(O)=O)=CC=C1OC1=CN=C(C=C(Cl)C=C2)C2=N1 ABOOPXYCKNFDNJ-SNVBAGLBSA-N 0.000 description 1
- MEFOUWRMVYJCQC-UHFFFAOYSA-N rimsulfuron Chemical compound CCS(=O)(=O)C1=CC=CN=C1S(=O)(=O)NC(=O)NC1=NC(OC)=CC(OC)=N1 MEFOUWRMVYJCQC-UHFFFAOYSA-N 0.000 description 1
- BUHNESFUCHPWED-UHFFFAOYSA-N s-[(4-methoxyphenyl)methyl] n,n-diethylcarbamothioate Chemical compound CCN(CC)C(=O)SCC1=CC=C(OC)C=C1 BUHNESFUCHPWED-UHFFFAOYSA-N 0.000 description 1
- LMHHRCOWPQNFTF-UHFFFAOYSA-N s-propan-2-yl azepane-1-carbothioate Chemical compound CC(C)SC(=O)N1CCCCCC1 LMHHRCOWPQNFTF-UHFFFAOYSA-N 0.000 description 1
- GNHDVXLWBQYPJE-UHFFFAOYSA-N saflufenacil Chemical compound C1=C(Cl)C(C(=O)NS(=O)(=O)N(C)C(C)C)=CC(N2C(N(C)C(=CC2=O)C(F)(F)F)=O)=C1F GNHDVXLWBQYPJE-UHFFFAOYSA-N 0.000 description 1
- 229940115128 sebex Drugs 0.000 description 1
- 239000003352 sequestering agent Substances 0.000 description 1
- 239000000377 silicon dioxide Substances 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- HKAMKLBXTLTVCN-UHFFFAOYSA-N simeton Chemical compound CCNC1=NC(NCC)=NC(OC)=N1 HKAMKLBXTLTVCN-UHFFFAOYSA-N 0.000 description 1
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- 239000000344 soap Substances 0.000 description 1
- PTLRDCMBXHILCL-UHFFFAOYSA-M sodium arsenite Chemical compound [Na+].[O-][As]=O PTLRDCMBXHILCL-UHFFFAOYSA-M 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- KZOJQMWTKJDSQJ-UHFFFAOYSA-M sodium;2,3-dibutylnaphthalene-1-sulfonate Chemical compound [Na+].C1=CC=C2C(S([O-])(=O)=O)=C(CCCC)C(CCCC)=CC2=C1 KZOJQMWTKJDSQJ-UHFFFAOYSA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
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- 230000007480 spreading Effects 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- PQTBTIFWAXVEPB-UHFFFAOYSA-N sulcotrione Chemical compound ClC1=CC(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O PQTBTIFWAXVEPB-UHFFFAOYSA-N 0.000 description 1
- OORLZFUTLGXMEF-UHFFFAOYSA-N sulfentrazone Chemical compound O=C1N(C(F)F)C(C)=NN1C1=CC(NS(C)(=O)=O)=C(Cl)C=C1Cl OORLZFUTLGXMEF-UHFFFAOYSA-N 0.000 description 1
- FZMKKCQHDROFNI-UHFFFAOYSA-N sulfometuron Chemical compound CC1=CC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 FZMKKCQHDROFNI-UHFFFAOYSA-N 0.000 description 1
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- IUQAXCIUEPFPSF-UHFFFAOYSA-N tembotrione Chemical compound ClC1=C(COCC(F)(F)F)C(S(=O)(=O)C)=CC=C1C(=O)C1C(=O)CCCC1=O IUQAXCIUEPFPSF-UHFFFAOYSA-N 0.000 description 1
- BCQMBFHBDZVHKU-UHFFFAOYSA-N terbumeton Chemical compound CCNC1=NC(NC(C)(C)C)=NC(OC)=N1 BCQMBFHBDZVHKU-UHFFFAOYSA-N 0.000 description 1
- IROINLKCQGIITA-UHFFFAOYSA-N terbutryn Chemical compound CCNC1=NC(NC(C)(C)C)=NC(SC)=N1 IROINLKCQGIITA-UHFFFAOYSA-N 0.000 description 1
- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-UHFFFAOYSA-N 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- XSKZXGDFSCCXQX-UHFFFAOYSA-N thiencarbazone-methyl Chemical compound COC(=O)C1=CSC(C)=C1S(=O)(=O)NC(=O)N1C(=O)N(C)C(OC)=N1 XSKZXGDFSCCXQX-UHFFFAOYSA-N 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 description 1
- DQFPEYARZIQXRM-LTGZKZEYSA-N tralkoxydim Chemical compound C1C(=O)C(C(/CC)=N/OCC)=C(O)CC1C1=C(C)C=C(C)C=C1C DQFPEYARZIQXRM-LTGZKZEYSA-N 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- WCLDITPGPXSPGV-UHFFFAOYSA-N tricamba Chemical compound COC1=C(Cl)C=C(Cl)C(Cl)=C1C(O)=O WCLDITPGPXSPGV-UHFFFAOYSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- 229940087291 tridecyl alcohol Drugs 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- ZSDSQXJSNMTJDA-UHFFFAOYSA-N trifluralin Chemical compound CCCN(CCC)C1=C([N+]([O-])=O)C=C(C(F)(F)F)C=C1[N+]([O-])=O ZSDSQXJSNMTJDA-UHFFFAOYSA-N 0.000 description 1
- AKTQJCBOGPBERP-UHFFFAOYSA-N triflusulfuron Chemical compound FC(F)(F)COC1=NC(N(C)C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2C)C(O)=O)=N1 AKTQJCBOGPBERP-UHFFFAOYSA-N 0.000 description 1
- PIHCREFCPDWIPY-UHFFFAOYSA-N tris[2-(2,4-dichlorophenoxy)ethyl] phosphite Chemical compound ClC1=CC(Cl)=CC=C1OCCOP(OCCOC=1C(=CC(Cl)=CC=1)Cl)OCCOC1=CC=C(Cl)C=C1Cl PIHCREFCPDWIPY-UHFFFAOYSA-N 0.000 description 1
- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
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- 239000000080 wetting agent Substances 0.000 description 1
- 235000005765 wild carrot Nutrition 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000008096 xylene 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
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/32—Ingredients for reducing the noxious effect of the active substances to organisms other than pests, e.g. toxicity reducing compositions, self-destructing compositions
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Dentistry (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Toxicology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161567413P | 2011-12-06 | 2011-12-06 | |
| US61/567,413 | 2011-12-06 | ||
| PCT/US2012/067942 WO2013085991A1 (en) | 2011-12-06 | 2012-12-05 | Herbicidal composition containing 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or derivative thereof and fluroxypyr or derivatives thereof |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2857974A1 true CA2857974A1 (en) | 2013-06-13 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA2857974A Abandoned CA2857974A1 (en) | 2011-12-06 | 2012-12-05 | Herbicidal composition containing 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl) pyridine-2-carboxylic acid or derivative thereof and fluroxypyr or derivatives thereof |
Country Status (26)
| Country | Link |
|---|---|
| US (1) | US20130143739A1 (enExample) |
| EP (1) | EP2787829B1 (enExample) |
| JP (2) | JP6621238B2 (enExample) |
| KR (1) | KR102065445B1 (enExample) |
| CN (1) | CN104105404B (enExample) |
| AR (1) | AR089094A1 (enExample) |
| AU (1) | AU2012347991B2 (enExample) |
| CA (1) | CA2857974A1 (enExample) |
| CO (1) | CO6970616A2 (enExample) |
| CR (1) | CR20140263A (enExample) |
| DK (1) | DK2787829T3 (enExample) |
| DO (1) | DOP2014000120A (enExample) |
| ES (1) | ES2599258T3 (enExample) |
| GT (1) | GT201400106A (enExample) |
| HU (1) | HUE030991T2 (enExample) |
| IL (1) | IL232978B (enExample) |
| IN (1) | IN2014DN04603A (enExample) |
| LT (1) | LT2787829T (enExample) |
| MX (1) | MX343558B (enExample) |
| NI (1) | NI201400053A (enExample) |
| PE (2) | PE20142045A1 (enExample) |
| PL (1) | PL2787829T3 (enExample) |
| RU (1) | RU2617346C2 (enExample) |
| UA (1) | UA116767C2 (enExample) |
| UY (1) | UY34491A (enExample) |
| WO (1) | WO2013085991A1 (enExample) |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| PL2787829T3 (pl) * | 2011-12-06 | 2017-08-31 | Dow Agrosciences Llc | Kompozycja chwastobójcza zawierająca kwas 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-metoksyfenylo)pirydyno-2-karboksylowy lub jego pochodną oraz fluroksypyr lub jego pochodną |
| KR102422133B1 (ko) * | 2013-10-11 | 2022-07-18 | 코르테바 애그리사이언스 엘엘씨 | 수성 제초 농축물 |
| JP2016539998A (ja) * | 2013-12-12 | 2016-12-22 | ダウ アグロサイエンシィズ エルエルシー | ハラウキシフェンによる選択的雑草防除 |
| KR102327844B1 (ko) * | 2014-01-15 | 2021-11-17 | 코르테바 애그리사이언스 엘엘씨 | 4-아미노-3-클로로-6-(4-클로로-2-플루오로-3-메톡시페닐)피리딘-2-카르복실산, 플루록시피르 및 페녹시 옥신을 함유하는 제초 조성물 |
| AR100785A1 (es) * | 2014-06-09 | 2016-11-02 | Dow Agrosciences Llc | Control herbicida de maleza a partir de combinaciones de fluroxipir e inhibidores de als |
| TWI689251B (zh) | 2014-09-15 | 2020-04-01 | 美商陶氏農業科學公司 | 源自於施用吡啶羧酸除草劑與合成生長素除草劑及/或生長素轉運抑制劑的協同性雜草控制 |
| MX2018015186A (es) * | 2016-06-10 | 2019-04-24 | Dow Agrosciences Llc | Composiciones herbicidas protegidas que contienen halauxifen y metodos de uso de estas en especies de brassica. |
| US20190075797A1 (en) * | 2017-08-25 | 2019-03-14 | Dow Agrosciences Llc | Safened Herbicidal compositions containing halauxifen or 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)-5-fluoropyridine-2-carboxylic acid and methods of use thereof in centipedegrass |
| CN113271777B (zh) * | 2018-11-02 | 2023-05-23 | 美国陶氏益农公司 | 包含氟氯吡啶酸和其他除草剂的组合物及其方法 |
| US12029217B2 (en) | 2018-11-06 | 2024-07-09 | Corteva Agriscience Llc | Safened compositions comprising pyridine carboxylate herbicides and isoxadifen |
| AU2019376614B2 (en) | 2018-11-06 | 2025-12-04 | Corteva Agriscience Llc | Safened compositions comprising pyridine carboxylate herbicides and cloquintocet |
| ES3013124T3 (en) | 2018-11-06 | 2025-04-11 | Corteva Agriscience Llc | Compositions comprising pyridine carboxylate herbicides and azole carboxylate safeners |
| CN113395900A (zh) | 2018-11-07 | 2021-09-14 | 科迪华农业科技有限责任公司 | 包含羧酸吡啶除草剂和4-羟基苯基-丙酮酸双加氧酶(hppd)抑制剂除草剂的组合物 |
| CA3118565A1 (en) | 2018-11-07 | 2020-05-14 | Corteva Agriscience Llc | Compositions comprising pyridine carboxylate herbicides with photosystem ii and optional hppd inhibitor herbicides |
| CN113271778B (zh) | 2018-11-07 | 2023-06-02 | 科迪华农业科技有限责任公司 | 包含羧酸吡啶除草剂和原卟啉原氧化酶(protox)抑制剂除草剂的组合物 |
| UA130218C2 (uk) | 2018-11-07 | 2025-12-24 | Кортева Аґрисайєнс Елелсі | Композиції, які містять гербіциди на основі піридинкарбоксилату з гербіцидами на основі інгібітора ацетолактатсинтази (als) |
| CA3118720A1 (en) * | 2018-11-07 | 2020-05-14 | Corteva Agriscience Llc | Compositions comprising a pyridine carboxylate herbicide and a microtubule assembly inhibitor herbicide |
| CN115363036A (zh) * | 2021-05-20 | 2022-11-22 | 四川利尔作物科学有限公司 | 含有苯唑草酮的除草剂组合物及其应用 |
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| EP0888056B1 (en) * | 1996-07-30 | 2002-10-09 | Basf Aktiengesellschaft | Herbicidal mixtures |
| RU2428416C2 (ru) * | 2006-01-13 | 2011-09-10 | Дау Агросайенсиз Ллс | 6-(полизамещенный арил)-4-аминопиколинаты и их применение в качестве гербицидов |
| RU2357416C2 (ru) * | 2007-08-06 | 2009-06-10 | Общество с ограниченной ответственностью "Сибагрохим" | Синергетическая гербицидная композиция в форме эмульгирующегося концентрата и способ борьбы с сорными растениями |
| PL2514314T3 (pl) * | 2007-08-27 | 2017-08-31 | Dow Agrosciences Llc | Synergistyczna kompozycja chwastobójcza zawierająca pewne kwasy pirydynokarboksylowe oraz pewne herbicydy stosowane w uprawie zbóż i ryżu |
| BRPI0921191B1 (pt) * | 2008-11-24 | 2023-01-31 | Dow Agrosciences Llc | Composição e método para proteção de trigo e cevada dos efeitos danosos de um herbicida de carboxilato de 6-(fenila trissubstituída)-4-amino-2- piridina |
| IN2012DN03298A (enExample) * | 2009-10-28 | 2015-10-23 | Dow Agrosciences Llc | |
| JP6151024B2 (ja) * | 2009-10-28 | 2017-06-21 | ダウ アグロサイエンシィズ エルエルシー | フルロキシピルおよびペノキススラム、ハロスルフロン−メチル、イマザモックスまたはイマゼタピルを含有する相乗的除草組成物 |
| ES2656156T3 (es) * | 2010-04-26 | 2018-02-23 | Dow Agrosciences, Llc | Dispersiones en aceite agrícolas estabilizadas |
| PL2787829T3 (pl) * | 2011-12-06 | 2017-08-31 | Dow Agrosciences Llc | Kompozycja chwastobójcza zawierająca kwas 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-metoksyfenylo)pirydyno-2-karboksylowy lub jego pochodną oraz fluroksypyr lub jego pochodną |
| UA120170C2 (uk) * | 2013-10-11 | 2019-10-25 | Дау Агросаєнсиз Елелсі | Водні гербіцидні концентрати |
| KR102422133B1 (ko) * | 2013-10-11 | 2022-07-18 | 코르테바 애그리사이언스 엘엘씨 | 수성 제초 농축물 |
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2012
- 2012-12-05 PL PL12854757T patent/PL2787829T3/pl unknown
- 2012-12-05 PE PE2014000869A patent/PE20142045A1/es not_active Application Discontinuation
- 2012-12-05 CA CA2857974A patent/CA2857974A1/en not_active Abandoned
- 2012-12-05 ES ES12854757.7T patent/ES2599258T3/es active Active
- 2012-12-05 AR ARP120104569A patent/AR089094A1/es active IP Right Grant
- 2012-12-05 US US13/705,899 patent/US20130143739A1/en not_active Abandoned
- 2012-12-05 CN CN201280068956.4A patent/CN104105404B/zh active Active
- 2012-12-05 AU AU2012347991A patent/AU2012347991B2/en active Active
- 2012-12-05 UA UAA201407533A patent/UA116767C2/uk unknown
- 2012-12-05 RU RU2014127534A patent/RU2617346C2/ru active
- 2012-12-05 EP EP12854757.7A patent/EP2787829B1/en active Active
- 2012-12-05 JP JP2014546022A patent/JP6621238B2/ja active Active
- 2012-12-05 DK DK12854757.7T patent/DK2787829T3/en active
- 2012-12-05 LT LTEP12854757.7T patent/LT2787829T/lt unknown
- 2012-12-05 KR KR1020147018318A patent/KR102065445B1/ko active Active
- 2012-12-05 IN IN4603DEN2014 patent/IN2014DN04603A/en unknown
- 2012-12-05 UY UY0001034491A patent/UY34491A/es active IP Right Grant
- 2012-12-05 WO PCT/US2012/067942 patent/WO2013085991A1/en not_active Ceased
- 2012-12-05 PE PE2018002001A patent/PE20181806A1/es unknown
- 2012-12-05 MX MX2014006730A patent/MX343558B/es active IP Right Grant
- 2012-12-05 HU HUE12854757A patent/HUE030991T2/en unknown
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2014
- 2014-06-02 CR CR20140263A patent/CR20140263A/es unknown
- 2014-06-04 GT GT201400106A patent/GT201400106A/es unknown
- 2014-06-05 DO DO2014000120A patent/DOP2014000120A/es unknown
- 2014-06-05 IL IL232978A patent/IL232978B/en active IP Right Grant
- 2014-06-05 NI NI201400053A patent/NI201400053A/es unknown
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2017
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Legal Events
| Date | Code | Title | Description |
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| EEER | Examination request |
Effective date: 20171201 |
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| FZDE | Discontinued |
Effective date: 20191205 |