EA019834B1 - Применение композиции, композиция для обработки семян, способ обработки семян и семена, обработанные композицией - Google Patents
Применение композиции, композиция для обработки семян, способ обработки семян и семена, обработанные композицией Download PDFInfo
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- EA019834B1 EA019834B1 EA201000322A EA201000322A EA019834B1 EA 019834 B1 EA019834 B1 EA 019834B1 EA 201000322 A EA201000322 A EA 201000322A EA 201000322 A EA201000322 A EA 201000322A EA 019834 B1 EA019834 B1 EA 019834B1
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- Eurasian Patent Office
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- composition
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- UBCKGWBNUIFUST-YHYXMXQVSA-N tetrachlorvinphos Chemical compound COP(=O)(OC)O\C(=C/Cl)C1=CC(Cl)=C(Cl)C=C1Cl UBCKGWBNUIFUST-YHYXMXQVSA-N 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
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-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
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 description 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 1
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 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
- SRVJKTDHMYAMHA-WUXMJOGZSA-N thioacetazone Chemical group CC(=O)NC1=CC=C(\C=N\NC(N)=S)C=C1 SRVJKTDHMYAMHA-WUXMJOGZSA-N 0.000 description 1
- 229960003231 thioacetazone Drugs 0.000 description 1
- 150000003556 thioamides Chemical class 0.000 description 1
- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical group COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-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
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 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
- IAQRGUVFOMOMEM-ONEGZZNKSA-N trans-but-2-ene Chemical compound C\C=C\C IAQRGUVFOMOMEM-ONEGZZNKSA-N 0.000 description 1
- 238000005809 transesterification reaction Methods 0.000 description 1
- DDVNRFNDOPPVQJ-HQJQHLMTSA-N transfluthrin Chemical compound CC1(C)[C@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=C(F)C(F)=CC(F)=C1F DDVNRFNDOPPVQJ-HQJQHLMTSA-N 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 125000005270 trialkylamine group Chemical group 0.000 description 1
- 125000005208 trialkylammonium group Chemical group 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
- 150000003852 triazoles Chemical class 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
- 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
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-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
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-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
- 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
- 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
- RKBCYCFRFCNLTO-UHFFFAOYSA-N triisopropylamine Chemical compound CC(C)N(C(C)C)C(C)C RKBCYCFRFCNLTO-UHFFFAOYSA-N 0.000 description 1
- LENZDBCJOHFCAS-UHFFFAOYSA-N tris Chemical compound OCC(N)(CO)CO LENZDBCJOHFCAS-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
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 150000003673 urethanes Chemical class 0.000 description 1
- 244000045561 useful plants Species 0.000 description 1
- JARYYMUOCXVXNK-CSLFJTBJSA-N validamycin A Chemical compound N([C@H]1C[C@@H]([C@H]([C@H](O)[C@H]1O)O[C@H]1[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O1)O)CO)[C@H]1C=C(CO)[C@@H](O)[C@H](O)[C@H]1O JARYYMUOCXVXNK-CSLFJTBJSA-N 0.000 description 1
- 239000010455 vermiculite Substances 0.000 description 1
- 229910052902 vermiculite Inorganic materials 0.000 description 1
- 235000019354 vermiculite Nutrition 0.000 description 1
- 230000035899 viability Effects 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 241000228158 x Triticosecale Species 0.000 description 1
- 239000005019 zein Substances 0.000 description 1
- 229940093612 zein Drugs 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- 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
-
- 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
- A01N25/02—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 containing liquids as carriers, diluents or solvents
- A01N25/04—Dispersions, emulsions, suspoemulsions, suspension concentrates or gels
-
- 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
- A01N25/30—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 characterised by the surfactants
-
- 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
-
- 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
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
- A01N43/647—Triazoles; Hydrogenated triazoles
- A01N43/653—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- 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
-
- 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
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Environmental Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pretreatment Of Seeds And Plants (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Preventing Corrosion Or Incrustation Of Metals (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07114462 | 2007-08-16 | ||
| PCT/EP2008/060672 WO2009021985A2 (en) | 2007-08-16 | 2008-08-14 | Seed treatment compositions and methods |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| EA201000322A1 EA201000322A1 (ru) | 2010-10-29 |
| EA019834B1 true EA019834B1 (ru) | 2014-06-30 |
Family
ID=40351221
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| EA201000322A EA019834B1 (ru) | 2007-08-16 | 2008-08-14 | Применение композиции, композиция для обработки семян, способ обработки семян и семена, обработанные композицией |
Country Status (18)
| Country | Link |
|---|---|
| US (2) | US9137984B2 (enExample) |
| EP (2) | EP2180783B1 (enExample) |
| JP (1) | JP2010536729A (enExample) |
| KR (1) | KR20100074129A (enExample) |
| CN (1) | CN101778561B (enExample) |
| AR (1) | AR068194A1 (enExample) |
| AU (1) | AU2008288385B2 (enExample) |
| BR (1) | BRPI0814941A2 (enExample) |
| CA (1) | CA2695417C (enExample) |
| CL (1) | CL2008002420A1 (enExample) |
| EA (1) | EA019834B1 (enExample) |
| IL (1) | IL203431A (enExample) |
| MX (1) | MX2010001666A (enExample) |
| NZ (2) | NZ583007A (enExample) |
| PL (2) | PL2180783T3 (enExample) |
| UA (1) | UA98802C2 (enExample) |
| WO (1) | WO2009021985A2 (enExample) |
| ZA (1) | ZA201001810B (enExample) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2611157C1 (ru) * | 2015-11-19 | 2017-02-21 | Алексей Георгиевич Бородкин | Состав для защиты семян астр, цинний и настурций от патогенных грибов |
Families Citing this family (55)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2683034A1 (en) * | 2007-04-25 | 2008-11-06 | Michael Stoesser | Alcohol alkoxylates, compositions containing these, and use of the alcohol alkoxylates as adjuvants for the agrochemical field |
| US9137984B2 (en) * | 2007-08-16 | 2015-09-22 | Basf Se | Seed treatment compositions and methods |
| US8097712B2 (en) | 2007-11-07 | 2012-01-17 | Beelogics Inc. | Compositions for conferring tolerance to viral disease in social insects, and the use thereof |
| MX2010006200A (es) | 2007-12-03 | 2010-12-06 | Valent Usa Corp | Formulaciones de tratamiento de semilla y metodos de uso. |
| US9101131B2 (en) | 2007-12-03 | 2015-08-11 | Valent U.S.A., Corporation | Seed treatment formulations |
| CN102066461A (zh) * | 2008-04-24 | 2011-05-18 | 巴斯夫欧洲公司 | 醇烷氧基化物、包含它们的试剂以及醇烷氧基化物在农化领域作为助剂的用途 |
| EP2408309A2 (de) * | 2009-03-19 | 2012-01-25 | Basf Se | Zusammensetzung enthaltend suspendiertes pestizid, salz und polysaccharid |
| CA2771006C (en) | 2009-08-14 | 2018-05-01 | Bayer Cropscience Ag | Aluminium silicate-free, highly concentrated suspension concentrates of metribuzin |
| AR078418A1 (es) | 2009-09-10 | 2011-11-09 | Univ Texas | Composiciones y metodos para controlar la estabilidad de surfactantes de etersulfato a temperaturas elevadas |
| US8962584B2 (en) | 2009-10-14 | 2015-02-24 | Yissum Research Development Company Of The Hebrew University Of Jerusalem, Ltd. | Compositions for controlling Varroa mites in bees |
| EP2525655B1 (en) * | 2010-01-22 | 2018-11-14 | Basf Se | A method for controlling arthropods |
| AU2011210837B2 (en) * | 2010-01-28 | 2014-06-05 | Board Of Regents, The University Of Texas System | Styrylphenol alkoxylate sulfate as a new surfactant composition for enhanced oil recovery applications |
| NZ627060A (en) | 2010-03-08 | 2016-01-29 | Monsanto Technology Llc | Polynucleotide molecules for gene regulation in plants |
| UA109282C2 (xx) * | 2010-07-09 | 2015-08-10 | Пестицидна суспензія на водній основі | |
| US10806146B2 (en) | 2011-09-13 | 2020-10-20 | Monsanto Technology Llc | Methods and compositions for weed control |
| WO2013040049A1 (en) | 2011-09-13 | 2013-03-21 | Monsanto Technology Llc | Methods and compositions for weed control |
| US10760086B2 (en) | 2011-09-13 | 2020-09-01 | Monsanto Technology Llc | Methods and compositions for weed control |
| US10829828B2 (en) | 2011-09-13 | 2020-11-10 | Monsanto Technology Llc | Methods and compositions for weed control |
| US9840715B1 (en) | 2011-09-13 | 2017-12-12 | Monsanto Technology Llc | Methods and compositions for delaying senescence and improving disease tolerance and yield in plants |
| AU2012308765B2 (en) | 2011-09-13 | 2018-06-21 | Monsanto Technology Llc | Methods and compositions for weed control |
| MX343071B (es) | 2011-09-13 | 2016-10-21 | Monsanto Technology Llc | Metodos y composiciones para el control de malezas. |
| EP2755466A4 (en) | 2011-09-13 | 2015-04-15 | Monsanto Technology Llc | METHOD AND COMPOSITIONS FOR WEED CONTROL |
| US9920326B1 (en) | 2011-09-14 | 2018-03-20 | Monsanto Technology Llc | Methods and compositions for increasing invertase activity in plants |
| CN104619843B (zh) | 2012-05-24 | 2020-03-06 | A.B.种子有限公司 | 用于使基因表达沉默的组合物和方法 |
| CN102746709A (zh) * | 2012-05-29 | 2012-10-24 | 吴江市屯村颜料厂 | 一种3118耐晒大红bbn的制备方法 |
| US10077451B2 (en) | 2012-10-18 | 2018-09-18 | Monsanto Technology Llc | Methods and compositions for plant pest control |
| CN102924166A (zh) * | 2012-10-23 | 2013-02-13 | 中国热带农业科学院热带生物技术研究所 | 一种甘蔗种茎包衣剂 |
| US10683505B2 (en) | 2013-01-01 | 2020-06-16 | Monsanto Technology Llc | Methods of introducing dsRNA to plant seeds for modulating gene expression |
| UY35251A (es) | 2013-01-01 | 2014-07-31 | Seeds Ltd Ab | MOLÉCULAS DE dsRNA AISLADAS Y MÉTODOS PARA USARLAS PARA SILENCIAR MOLÉCULAS DIANA DE INTERÉS |
| US10000767B2 (en) | 2013-01-28 | 2018-06-19 | Monsanto Technology Llc | Methods and compositions for plant pest control |
| JP6370318B2 (ja) | 2013-02-22 | 2018-08-08 | バレント・ユーエスエイ・コーポレイションValent U.S.A., Corporation | 種子処理製剤 |
| EP2967082A4 (en) | 2013-03-13 | 2016-11-02 | Monsanto Technology Llc | METHOD AND COMPOSITIONS FOR WEED CONTROL |
| EP3604535A3 (en) | 2013-03-13 | 2020-04-22 | Monsanto Technology LLC | Methods and compositions for weed control |
| US20140283211A1 (en) | 2013-03-14 | 2014-09-18 | Monsanto Technology Llc | Methods and Compositions for Plant Pest Control |
| US10568328B2 (en) | 2013-03-15 | 2020-02-25 | Monsanto Technology Llc | Methods and compositions for weed control |
| US9850496B2 (en) | 2013-07-19 | 2017-12-26 | Monsanto Technology Llc | Compositions and methods for controlling Leptinotarsa |
| EP3030663B1 (en) | 2013-07-19 | 2019-09-04 | Monsanto Technology LLC | Compositions and methods for controlling leptinotarsa |
| MX390055B (es) | 2013-11-04 | 2025-03-20 | Monsanto Technology Llc | Composiciones y metodos para controlar infestaciones de plagas y parasitos de los artropodos. |
| UA119253C2 (uk) | 2013-12-10 | 2019-05-27 | Біолоджикс, Інк. | Спосіб боротьби із вірусом у кліща varroa та у бджіл |
| US10334848B2 (en) | 2014-01-15 | 2019-07-02 | Monsanto Technology Llc | Methods and compositions for weed control using EPSPS polynucleotides |
| EP3125676A4 (en) | 2014-04-01 | 2018-02-14 | Monsanto Technology LLC | Compositions and methods for controlling insect pests |
| EP2932842A1 (en) * | 2014-04-16 | 2015-10-21 | Syngenta Participations AG. | Rice seed treatment composition and method |
| US10988764B2 (en) | 2014-06-23 | 2021-04-27 | Monsanto Technology Llc | Compositions and methods for regulating gene expression via RNA interference |
| WO2015200539A1 (en) | 2014-06-25 | 2015-12-30 | Monsanto Technology Llc | Methods and compositions for delivering nucleic acids to plant cells and regulating gene expression |
| CN114009454A (zh) | 2014-07-29 | 2022-02-08 | 孟山都技术公司 | 用于控制昆虫害虫的组合物和方法 |
| CN106998678B (zh) | 2014-12-09 | 2021-02-26 | 巴斯夫欧洲公司 | 农药和含有可共聚表面活性剂的聚合物颗粒的水分散体 |
| MX395326B (es) | 2015-01-22 | 2025-03-25 | Monsanto Technology Llc | Composiciones y métodos para controlar leptinotarsa. |
| CN107750125A (zh) | 2015-06-02 | 2018-03-02 | 孟山都技术有限公司 | 用于将多核苷酸递送至植物中的组合物和方法 |
| CN108024517A (zh) | 2015-06-03 | 2018-05-11 | 孟山都技术公司 | 用于将核酸引入到植物中的方法和组合物 |
| EP3534707A4 (en) | 2016-11-02 | 2020-09-16 | Paramount Products 1 LLC | ADJUVANT COMPOSITIONS FOR PLANT TREATMENT CHEMICALS |
| WO2018156457A1 (en) | 2017-02-24 | 2018-08-30 | Paramount Products 1 Llc | Treatment for plants in conjunction with harvesting |
| BR112022002909A2 (pt) | 2019-08-20 | 2022-05-10 | Bayer Ag | Suspensões concentradas de metribuzin e diflufenicam altamente concentradas e sem cristalização |
| CA3152853A1 (en) * | 2019-10-28 | 2021-05-06 | Jane Liu | Novel clothianidin compositions and methods of use thereof |
| GB202102142D0 (en) * | 2021-02-16 | 2021-03-31 | Upl Corporation Ltd | Stable fungicidal compositions |
| WO2024154137A1 (en) * | 2023-01-19 | 2024-07-25 | Adama Makhteshim Ltd. | Aqueous fungicide mixture formulation with enhanced activities |
Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000035284A1 (en) * | 1998-12-17 | 2000-06-22 | Syngenta Participations Ag . | Pesticidal aqueous suspension concentrates |
| WO2002019821A1 (en) * | 2000-09-05 | 2002-03-14 | Syngenta Limited | Pesticidal formulations |
| WO2005036963A1 (de) * | 2003-09-23 | 2005-04-28 | Bayer Cropscience Aktiengesellschaft | Suspensionskonzentrate |
| WO2006035316A2 (en) * | 2005-04-25 | 2006-04-06 | Syngenta Participations Ag | Fungicidal aqueous compositions for seed treatment |
| WO2007003319A2 (en) * | 2005-06-30 | 2007-01-11 | Syngenta Participations Ag | Seed treatment method and pesticidal composition |
| WO2008061899A2 (en) * | 2006-11-22 | 2008-05-29 | Basf Se | Liquid water based agrochemical formulations |
| WO2008136917A1 (en) * | 2007-05-04 | 2008-11-13 | Troy Technology Corporation, Inc. | Water-based antimicrobially active, dispersion concentrates |
Family Cites Families (78)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3060084A (en) | 1961-06-09 | 1962-10-23 | Du Pont | Improved homogeneous, readily dispersed, pesticidal concentrate |
| US3299566A (en) | 1964-06-01 | 1967-01-24 | Olin Mathieson | Water soluble film containing agricultural chemicals |
| US4144050A (en) | 1969-02-05 | 1979-03-13 | Hoechst Aktiengesellschaft | Micro granules for pesticides and process for their manufacture |
| US3920442A (en) | 1972-09-18 | 1975-11-18 | Du Pont | Water-dispersible pesticide aggregates |
| US4172714A (en) | 1976-12-20 | 1979-10-30 | E. I. Du Pont De Nemours And Company | Dry compactible, swellable herbicidal compositions and pellets produced therefrom |
| DE2840501A1 (de) | 1978-09-18 | 1980-03-27 | Basf Ag | Verfahren zur herstellung von copolymerisaten aus maleinsaeureanhydrid und alkenen |
| DE2840502A1 (de) | 1978-09-18 | 1980-03-27 | Basf Ag | Verfahren zur herstellung von terpolymeren |
| US4272417A (en) | 1979-05-22 | 1981-06-09 | Cargill, Incorporated | Stable protective seed coating |
| US4245432A (en) | 1979-07-25 | 1981-01-20 | Eastman Kodak Company | Seed coatings |
| US4339456A (en) | 1980-01-14 | 1982-07-13 | Gustafson, Inc. | Peanut seed treating |
| GB2095558B (en) | 1981-03-30 | 1984-10-24 | Avon Packers Ltd | Formulation of agricultural chemicals |
| US4383391A (en) | 1981-09-21 | 1983-05-17 | Celanese Corporation | Seed coating composition based on carbamate pesticide and non-alkaline amorphous carbon |
| US4634587A (en) | 1982-07-09 | 1987-01-06 | Key Pharmaceuticals, Inc. | Sustained release quinidine dosage form |
| US4465017A (en) | 1983-03-09 | 1984-08-14 | Simmons John J | Seed coating machine |
| US4735015A (en) | 1983-11-25 | 1988-04-05 | Basf Corporation | Seed protective coating |
| DE3616010A1 (de) | 1986-05-13 | 1987-11-19 | Bayer Ag | Verfahren zum beizen und/oder inkrustieren von saatgutkoernern |
| DE3700535A1 (de) | 1987-01-10 | 1988-07-21 | Basf Ag | Verfahren zur herstellung von wasserloeslichen copoylmerisaten der maleinsaeure und deren verwendung als wasserbehandlungsmittel |
| FR2618041B1 (fr) | 1987-07-16 | 1991-06-21 | Ceres Ets | Dispositif pour le traitement des semences |
| KR900003088B1 (ko) | 1988-03-26 | 1990-05-07 | 재단법인 한국화학연구소 | 5-하이드록시피라졸 유도체 |
| US5180587A (en) | 1988-06-28 | 1993-01-19 | E. I. Du Pont De Nemours And Company | Tablet formulations of pesticides |
| JPH0646887B2 (ja) | 1988-11-08 | 1994-06-22 | 矢崎総業株式会社 | 種子のゲル被覆装置 |
| US5300127A (en) | 1989-01-06 | 1994-04-05 | Agricultural Genetics Company Limited | Seed coatings |
| ES2166919T3 (es) | 1989-08-30 | 2002-05-01 | Kynoch Agrochemicals Proprieta | Preparacion de un dispositivo dosificador. |
| BR9106147A (pt) | 1990-03-12 | 1993-03-09 | Du Pont | Granulos de pesticidas dispersaveis em agua ou soluveis em agua feitos a partir de ligantes termo-ativados |
| US5169951A (en) | 1990-04-23 | 1992-12-08 | Ciba-Geigy Corporation | Process for preparing nematicidal compositions |
| ES2089056T3 (es) | 1990-06-16 | 1996-10-01 | Nihon Nohyaku Co Ltd | Derivados de hidrazincarboxamida, un procedimiento para la produccion de los mismos, y usos de los mismos. |
| ES2091878T3 (es) | 1990-10-11 | 1996-11-16 | Sumitomo Chemical Co | Composicion plaguicida. |
| CA2113643C (en) | 1991-07-19 | 2003-04-22 | Ikbal A. Akhtar | Seed film compositions |
| SK44894A3 (en) | 1991-10-18 | 1995-04-12 | Monsanto Co | Trisubstituted aromatic compounds, method of their preparation and fungicidal agents |
| FI93687C (fi) | 1992-07-29 | 1995-05-26 | Novasso Oy | Menetelmä siementen päällystämiseksi |
| US5661103A (en) | 1992-11-05 | 1997-08-26 | Donlar Corporation | Seed treatment composition and method |
| DE4322211A1 (de) | 1993-07-03 | 1995-01-12 | Basf Ag | Wäßrige, mehrphasige, stabile Fertigformulierung für Pflanzenschutz-Wirkstoffe und Verfahren zu ihrer Herstellung |
| GB9319129D0 (en) * | 1993-09-15 | 1993-11-03 | Dowelanco Ltd | Storage and dilution of stable aqueous dispersions |
| US5882713A (en) | 1994-04-26 | 1999-03-16 | The United States Of America As Represented By The Secretary Of Agriculture | Non-separable compositions of starch and water-immiscible organic materials |
| DE19505995A1 (de) | 1995-02-21 | 1996-08-22 | Degussa | Verfahren zur Herstellung von Thietanonen |
| US5580544A (en) | 1995-03-29 | 1996-12-03 | Uniroyal Chemical Company, Inc. | Paste formulation useful for seed treatment and foliar treatment of plants |
| JP3125847B2 (ja) | 1995-06-15 | 2001-01-22 | 矢崎総業株式会社 | ゲル被覆種子のゲル層易崩壊処理方法 |
| US5622003A (en) | 1995-07-11 | 1997-04-22 | Isp Investments Inc. | Seed coating containing Mn (NO3)2 ·6H2 O |
| AU1670997A (en) | 1996-04-26 | 1997-11-19 | Nippon Soda Co., Ltd. | Novel benzene derivatives substituted by heterocycles and herbicides |
| AU1670797A (en) | 1996-04-26 | 1997-11-19 | Nippon Soda Co., Ltd. | Benzene derivatives substituted by heterocycles and herbicides |
| BR9708828A (pt) | 1996-04-26 | 1999-08-03 | Nippon Soda Co | Composto e composição herbicida |
| US5876739A (en) | 1996-06-13 | 1999-03-02 | Novartis Ag | Insecticidal seed coating |
| US5849320A (en) | 1996-06-13 | 1998-12-15 | Novartis Corporation | Insecticidal seed coating |
| US5939356A (en) | 1996-06-21 | 1999-08-17 | Southwest Research Institute | Controlled release coated agricultural products |
| AP1004A (en) | 1996-12-24 | 2001-08-28 | Rhone Poulenc Agrochimie | Pesticidal 1-aryl and pyridylpyrazole derivatives. |
| DE69738328T2 (de) | 1996-12-24 | 2008-11-27 | Merial Ltd., Harlow | Pestizide 1-arylpyrazole |
| JP3185133B2 (ja) | 1997-02-13 | 2001-07-09 | タキイ種苗株式会社 | 造粒コーティング種子およびその製造方法 |
| ES2327189T3 (es) | 1997-04-07 | 2009-10-26 | Nihon Nohyaku Co., Ltd. | Derivados de pirazol, su procedimiento de preparacion, intermediarios y plangicida que los contienen como ingrediente activo. |
| US5891246A (en) | 1997-08-15 | 1999-04-06 | Gustafson, Inc. | Seed coating apparatus |
| MY118564A (en) * | 1998-02-10 | 2004-12-31 | Syngenta Participations Ag | Pesticidal compositions |
| US6096769A (en) | 1998-04-20 | 2000-08-01 | American Cyanamid Company | Fungicidal co-formulation |
| WO2000058085A1 (en) * | 1999-03-31 | 2000-10-05 | Penford Corporation | Packaging and structural materials comprising potato peel waste |
| EP1197492B1 (en) | 1999-06-29 | 2007-09-05 | Nihon Nohyaku Co., Ltd. | Pyrazole derivatives and process for producing the same, and pesticides containing the same as the active ingredient |
| US6221890B1 (en) | 1999-10-21 | 2001-04-24 | Sumitomo Chemical Company Limited | Acaricidal compositions |
| MY138097A (en) | 2000-03-22 | 2009-04-30 | Du Pont | Insecticidal anthranilamides |
| WO2002048137A2 (en) | 2000-12-11 | 2002-06-20 | E. I. Du Pont De Nemours And Company | Substituted heterocyclic phthalic acid diamide arthropodicides |
| JP2002193709A (ja) | 2000-12-27 | 2002-07-10 | Mitsubishi Chemicals Corp | 殺虫・殺菌剤組成物 |
| JP2002284608A (ja) | 2001-01-18 | 2002-10-03 | Sumitomo Chem Co Ltd | 殺虫剤および殺虫方法 |
| JP4269574B2 (ja) | 2001-05-09 | 2009-05-27 | 住友化学株式会社 | マロノニトリル化合物及びその用途 |
| JP2003026521A (ja) | 2001-07-11 | 2003-01-29 | Sumitomo Chem Co Ltd | 殺虫・殺線虫剤組成物 |
| JP2003026520A (ja) | 2001-07-11 | 2003-01-29 | Sumitomo Chem Co Ltd | 殺虫・殺線虫剤組成物 |
| MY142967A (en) | 2001-08-13 | 2011-01-31 | Du Pont | Method for controlling particular insect pests by applying anthranilamide compounds |
| TWI283164B (en) | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
| CN100343233C (zh) | 2002-07-17 | 2007-10-17 | 住友化学株式会社 | 丙二腈化合物及其用途 |
| JP4457588B2 (ja) | 2002-07-17 | 2010-04-28 | 住友化学株式会社 | マロノニトリル化合物の用途 |
| AR041052A1 (es) | 2002-08-29 | 2005-04-27 | Sumitomo Metal Ind | Compuesto de malononitrilo, uso del mismo para controlar plagas y composicion pesticida en base al mismo |
| CN100349901C (zh) | 2002-10-04 | 2007-11-21 | 纳幕尔杜邦公司 | 邻氨基苯甲酰胺杀虫剂 |
| JP3764895B1 (ja) | 2003-01-28 | 2006-04-12 | イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー | シアノアントラニルアミド殺虫剤 |
| JP2004269479A (ja) | 2003-03-12 | 2004-09-30 | Otsuka Chemical Co Ltd | 殺ダニ剤組成物 |
| BRPI0418173A (pt) | 2003-12-26 | 2007-04-27 | Sumitomo Chemical Co | composto de nitrila e seu uso em controle de peste |
| KR101121407B1 (ko) | 2004-01-16 | 2012-04-12 | 스미또모 가가꾸 가부시끼가이샤 | 살충제로서의 말로노니트릴 화합물 |
| US7541374B2 (en) | 2004-01-16 | 2009-06-02 | Sumitomo Chemical Company, Limited | Malononitrile compounds and use thereof |
| MY144494A (en) | 2004-03-16 | 2011-09-30 | Syngenta Participations Ag | Seed treatment pesticidal compositions. |
| RU2006139953A (ru) | 2004-04-13 | 2008-05-20 | Е.И. Дюпон Де Немур Энд Компани (Us) | Антраниламидные инсектициды |
| AR056077A1 (es) * | 2005-09-19 | 2007-09-19 | Syngenta Participations Ag | Metodos mejorados para el control de plagas de tierra y/o enfermedades surgidas de la tierra |
| JP2009010907A (ja) | 2007-05-25 | 2009-01-15 | Shintaro Gomi | アクティブコイル、アクティブコイルアンテナエレメント及びlc共振回路並びにそれらを利用した放送用受信機。 |
| WO2009021717A2 (en) * | 2007-08-14 | 2009-02-19 | Syngenta Participations Ag | Pesticidal formulation |
| US9137984B2 (en) * | 2007-08-16 | 2015-09-22 | Basf Se | Seed treatment compositions and methods |
-
2008
- 2008-08-14 US US12/672,751 patent/US9137984B2/en active Active
- 2008-08-14 PL PL08803029T patent/PL2180783T3/pl unknown
- 2008-08-14 UA UAA201002973A patent/UA98802C2/ru unknown
- 2008-08-14 NZ NZ58300708A patent/NZ583007A/xx unknown
- 2008-08-14 JP JP2010520580A patent/JP2010536729A/ja active Pending
- 2008-08-14 WO PCT/EP2008/060672 patent/WO2009021985A2/en not_active Ceased
- 2008-08-14 CL CL2008002420A patent/CL2008002420A1/es unknown
- 2008-08-14 EA EA201000322A patent/EA019834B1/ru not_active IP Right Cessation
- 2008-08-14 CN CN2008801031813A patent/CN101778561B/zh active Active
- 2008-08-14 PL PL16192502T patent/PL3150068T3/pl unknown
- 2008-08-14 BR BRPI0814941 patent/BRPI0814941A2/pt not_active Application Discontinuation
- 2008-08-14 EP EP08803029.1A patent/EP2180783B1/en active Active
- 2008-08-14 CA CA2695417A patent/CA2695417C/en active Active
- 2008-08-14 EP EP16192502.9A patent/EP3150068B1/en active Active
- 2008-08-14 NZ NZ59999708A patent/NZ599997A/xx unknown
- 2008-08-14 MX MX2010001666A patent/MX2010001666A/es unknown
- 2008-08-14 KR KR1020107005674A patent/KR20100074129A/ko not_active Ceased
- 2008-08-14 AU AU2008288385A patent/AU2008288385B2/en active Active
- 2008-08-15 AR ARP080103597 patent/AR068194A1/es active IP Right Grant
-
2010
- 2010-01-21 IL IL203431A patent/IL203431A/en active IP Right Grant
- 2010-03-15 ZA ZA2010/01810A patent/ZA201001810B/en unknown
-
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- 2015-08-14 US US14/826,381 patent/US20150342182A1/en not_active Abandoned
Patent Citations (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2000035284A1 (en) * | 1998-12-17 | 2000-06-22 | Syngenta Participations Ag . | Pesticidal aqueous suspension concentrates |
| WO2002019821A1 (en) * | 2000-09-05 | 2002-03-14 | Syngenta Limited | Pesticidal formulations |
| WO2005036963A1 (de) * | 2003-09-23 | 2005-04-28 | Bayer Cropscience Aktiengesellschaft | Suspensionskonzentrate |
| WO2006035316A2 (en) * | 2005-04-25 | 2006-04-06 | Syngenta Participations Ag | Fungicidal aqueous compositions for seed treatment |
| WO2007003319A2 (en) * | 2005-06-30 | 2007-01-11 | Syngenta Participations Ag | Seed treatment method and pesticidal composition |
| WO2008061899A2 (en) * | 2006-11-22 | 2008-05-29 | Basf Se | Liquid water based agrochemical formulations |
| WO2008136917A1 (en) * | 2007-05-04 | 2008-11-13 | Troy Technology Corporation, Inc. | Water-based antimicrobially active, dispersion concentrates |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| RU2611157C1 (ru) * | 2015-11-19 | 2017-02-21 | Алексей Георгиевич Бородкин | Состав для защиты семян астр, цинний и настурций от патогенных грибов |
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| AU2008288385B2 (en) | 2013-11-07 |
| WO2009021985A3 (en) | 2009-12-30 |
| EP2180783A2 (en) | 2010-05-05 |
| EP3150068A1 (en) | 2017-04-05 |
| MX2010001666A (es) | 2010-03-10 |
| NZ583007A (en) | 2012-06-29 |
| US20110166022A1 (en) | 2011-07-07 |
| PL3150068T3 (pl) | 2020-04-30 |
| KR20100074129A (ko) | 2010-07-01 |
| CL2008002420A1 (es) | 2009-10-23 |
| CN101778561A (zh) | 2010-07-14 |
| AR068194A1 (es) | 2009-11-11 |
| AU2008288385A1 (en) | 2009-02-19 |
| CA2695417A1 (en) | 2009-02-19 |
| BRPI0814941A2 (pt) | 2014-09-30 |
| EA201000322A1 (ru) | 2010-10-29 |
| IL203431A (en) | 2017-04-30 |
| US9137984B2 (en) | 2015-09-22 |
| US20150342182A1 (en) | 2015-12-03 |
| ZA201001810B (en) | 2011-05-25 |
| UA98802C2 (ru) | 2012-06-25 |
| PL2180783T3 (pl) | 2017-08-31 |
| EP2180783B1 (en) | 2017-02-22 |
| CA2695417C (en) | 2015-10-06 |
| NZ599997A (en) | 2013-08-30 |
| CN101778561B (zh) | 2013-12-25 |
| WO2009021985A2 (en) | 2009-02-19 |
| EP3150068B1 (en) | 2019-10-09 |
| JP2010536729A (ja) | 2010-12-02 |
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