AU2003232505B2 - Use of defined alcohol alkoxylates as adjuvants in the agrotechnical field - Google Patents
Use of defined alcohol alkoxylates as adjuvants in the agrotechnical field Download PDFInfo
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- AU2003232505B2 AU2003232505B2 AU2003232505A AU2003232505A AU2003232505B2 AU 2003232505 B2 AU2003232505 B2 AU 2003232505B2 AU 2003232505 A AU2003232505 A AU 2003232505A AU 2003232505 A AU2003232505 A AU 2003232505A AU 2003232505 B2 AU2003232505 B2 AU 2003232505B2
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- zero
- alkoxylates
- alcohol
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- ITDJKCJYYAQMRO-UHFFFAOYSA-L rhodium(2+);diacetate Chemical compound [Rh+2].CC([O-])=O.CC([O-])=O ITDJKCJYYAQMRO-UHFFFAOYSA-L 0.000 description 1
- PZSJYEAHAINDJI-UHFFFAOYSA-N rhodium(3+) Chemical class [Rh+3] PZSJYEAHAINDJI-UHFFFAOYSA-N 0.000 description 1
- VXNYVYJABGOSBX-UHFFFAOYSA-N rhodium(3+);trinitrate Chemical compound [Rh+3].[O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O VXNYVYJABGOSBX-UHFFFAOYSA-N 0.000 description 1
- YWFDDXXMOPZFFM-UHFFFAOYSA-H rhodium(3+);trisulfate Chemical compound [Rh+3].[Rh+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O YWFDDXXMOPZFFM-UHFFFAOYSA-H 0.000 description 1
- SONJTKJMTWTJCT-UHFFFAOYSA-K rhodium(iii) chloride Chemical compound [Cl-].[Cl-].[Cl-].[Rh+3] SONJTKJMTWTJCT-UHFFFAOYSA-K 0.000 description 1
- 210000000614 rib Anatomy 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
- 150000003304 ruthenium compounds Chemical class 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
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- 239000004576 sand Substances 0.000 description 1
- 108700004121 sarkosyl Proteins 0.000 description 1
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
- 238000004062 sedimentation Methods 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- LIVNPJMFVYWSIS-UHFFFAOYSA-N silicon monoxide Chemical class [Si-]#[O+] LIVNPJMFVYWSIS-UHFFFAOYSA-N 0.000 description 1
- 229910052814 silicon oxide Inorganic materials 0.000 description 1
- ODCWYMIRDDJXKW-UHFFFAOYSA-N simazine Chemical compound CCNC1=NC(Cl)=NC(NCC)=N1 ODCWYMIRDDJXKW-UHFFFAOYSA-N 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- KSAVQLQVUXSOCR-UHFFFAOYSA-M sodium lauroyl sarcosinate Chemical compound [Na+].CCCCCCCCCCCC(=O)N(C)CC([O-])=O KSAVQLQVUXSOCR-UHFFFAOYSA-M 0.000 description 1
- 229940045885 sodium lauroyl sarcosinate Drugs 0.000 description 1
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 description 1
- 239000001593 sorbitan monooleate Substances 0.000 description 1
- 235000011069 sorbitan monooleate Nutrition 0.000 description 1
- 229940035049 sorbitan monooleate Drugs 0.000 description 1
- 239000001589 sorbitan tristearate Substances 0.000 description 1
- 235000011078 sorbitan tristearate Nutrition 0.000 description 1
- 229960004129 sorbitan tristearate Drugs 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 230000006641 stabilisation Effects 0.000 description 1
- 238000011105 stabilization Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 125000004079 stearyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 239000000758 substrate Substances 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
- ZDXMLEQEMNLCQG-UHFFFAOYSA-N sulfometuron methyl Chemical group COC(=O)C1=CC=CC=C1S(=O)(=O)NC(=O)NC1=NC(C)=CC(C)=N1 ZDXMLEQEMNLCQG-UHFFFAOYSA-N 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 150000003462 sulfoxides Chemical class 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- ZZYSLNWGKKDOML-UHFFFAOYSA-N tebufenpyrad Chemical compound CCC1=NN(C)C(C(=O)NCC=2C=CC(=CC=2)C(C)(C)C)=C1Cl ZZYSLNWGKKDOML-UHFFFAOYSA-N 0.000 description 1
- WWJZWCUNLNYYAU-UHFFFAOYSA-N temephos Chemical compound C1=CC(OP(=S)(OC)OC)=CC=C1SC1=CC=C(OP(=S)(OC)OC)C=C1 WWJZWCUNLNYYAU-UHFFFAOYSA-N 0.000 description 1
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 125000005329 tetralinyl group Chemical class C1(CCCC2=CC=CC=C12)* 0.000 description 1
- 239000004753 textile 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
- 239000002562 thickening agent Substances 0.000 description 1
- AHTPATJNIAFOLR-UHFFFAOYSA-N thifensulfuron-methyl Chemical group S1C=CC(S(=O)(=O)NC(=O)NC=2N=C(OC)N=C(C)N=2)=C1C(=O)OC AHTPATJNIAFOLR-UHFFFAOYSA-N 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- YFNCATAIYKQPOO-UHFFFAOYSA-N thiophanate Chemical compound CCOC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OCC YFNCATAIYKQPOO-UHFFFAOYSA-N 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 231100000027 toxicology Toxicity 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
- 150000003626 triacylglycerols Chemical class 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
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-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
- IMEVJVISCHQJRM-UHFFFAOYSA-N triflusulfuron-methyl Chemical group COC(=O)C1=CC=CC(C)=C1S(=O)(=O)NC(=O)NC1=NC(OCC(F)(F)F)=NC(N(C)C)=N1 IMEVJVISCHQJRM-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
- 238000005829 trimerization reaction Methods 0.000 description 1
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 235000019871 vegetable fat Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
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- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000002351 wastewater Substances 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- AMHNZOICSMBGDH-UHFFFAOYSA-L zineb Chemical compound [Zn+2].[S-]C(=S)NCCNC([S-])=S AMHNZOICSMBGDH-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
- 229910052726 zirconium Inorganic materials 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
- A01N25/30—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
- A01N31/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic oxygen or sulfur compounds
- A01N31/02—Acyclic compounds
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Cultivation Of Plants (AREA)
- Fertilizers (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2009240808A AU2009240808B2 (en) | 2002-04-24 | 2009-11-25 | Use of defined alcohol alkoxylates as adjuvants |
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10218316.3 | 2002-04-24 | ||
| DE10218316 | 2002-04-24 | ||
| PCT/EP2003/004276 WO2003090531A1 (de) | 2002-04-24 | 2003-04-24 | Verwendung bestimmter alkoholalkoxylate als adjuvans für den agrotechnischen bereich |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2009240808A Division AU2009240808B2 (en) | 2002-04-24 | 2009-11-25 | Use of defined alcohol alkoxylates as adjuvants |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2003232505A1 AU2003232505A1 (en) | 2003-11-10 |
| AU2003232505B2 true AU2003232505B2 (en) | 2009-08-27 |
Family
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|---|---|---|---|
| AU2003232505A Expired AU2003232505B2 (en) | 2002-04-24 | 2003-04-24 | Use of defined alcohol alkoxylates as adjuvants in the agrotechnical field |
| AU2009240808A Ceased AU2009240808B2 (en) | 2002-04-24 | 2009-11-25 | Use of defined alcohol alkoxylates as adjuvants |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2009240808A Ceased AU2009240808B2 (en) | 2002-04-24 | 2009-11-25 | Use of defined alcohol alkoxylates as adjuvants |
Country Status (24)
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| EP (2) | EP1501355B1 (enExample) |
| JP (1) | JP4417118B2 (enExample) |
| KR (1) | KR100983437B1 (enExample) |
| CN (1) | CN100370900C (enExample) |
| AT (1) | ATE468016T1 (enExample) |
| AU (2) | AU2003232505B2 (enExample) |
| BR (2) | BR122013024224B1 (enExample) |
| CA (2) | CA2697544C (enExample) |
| CY (1) | CY1110732T1 (enExample) |
| DE (1) | DE50312724D1 (enExample) |
| DK (1) | DK1501355T3 (enExample) |
| EA (2) | EA011649B1 (enExample) |
| ES (1) | ES2345980T3 (enExample) |
| IL (2) | IL164524A (enExample) |
| IN (1) | IN2004CH02386A (enExample) |
| MX (1) | MXPA04010344A (enExample) |
| NZ (1) | NZ536029A (enExample) |
| PL (2) | PL211842B1 (enExample) |
| PT (1) | PT1501355E (enExample) |
| SI (1) | SI1501355T1 (enExample) |
| UA (1) | UA82192C2 (enExample) |
| WO (1) | WO2003090531A1 (enExample) |
| ZA (1) | ZA200409411B (enExample) |
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| PL1988986T3 (pl) * | 2006-02-22 | 2010-05-31 | Basf Se | Mieszanina powierzchniowo czynna zawierająca składniki krótkołańcuchowe oraz długołańcuchowe |
| UA89599C2 (uk) * | 2006-08-04 | 2010-02-10 | Басф Се | Водний концентрат діючої речовини з гербіцидною дією та спосіб боротьби з небажаним ростом рослин |
| AR064177A1 (es) * | 2006-12-07 | 2009-03-18 | Basf Ag | Composiciones y kits que comprenden un triazol fungicida y un alcohol alcoxilado, y sus usos |
| EP2150515B1 (de) * | 2007-04-25 | 2016-08-24 | Basf Se | Alkoholalkoxylate, diese enthaltende mittel und verwendung der alkoholalkoxylate als adjuvans für den agrochemischen bereich |
| ES2323399B2 (es) * | 2007-06-19 | 2010-02-26 | Gat Microencapsulation Ag | Suspensiones en aceites de sulfonilureas y combinaciones agroquimicas. |
| BRPI0814420A2 (pt) * | 2007-07-20 | 2015-11-17 | Basf Se | composição, e, uso de álcool alcoxilado. |
| EP2271697B1 (de) | 2008-04-24 | 2014-07-09 | Basf Se | Alkoholalkoxylate, diese enthaltende mittel und verwendung der alkoholalkoxylate als adjuvans für den agrochemischen bereich |
| WO2009130282A2 (de) * | 2008-04-24 | 2009-10-29 | Basf Se | Cyclodextrin-haltige suspensionskonzentrate, verfahren zu ihrer herstellung und ihre verwendung |
| EP2147599A1 (en) * | 2008-07-23 | 2010-01-27 | Cognis IP Management GmbH | Agricultural compositions |
| EP2334174B1 (de) | 2008-09-26 | 2012-09-19 | Basf Se | Flüssige, in wasser emulgierbare wirkstoffkonzentrate |
| DE102008043185A1 (de) * | 2008-10-27 | 2010-04-29 | Evonik Goldschmidt Gmbh | Nicht schäumende organische Tenside als Additive für Tankmischungszubereitungen im Pflanzenschutz |
| FR2949643B1 (fr) * | 2009-09-08 | 2012-09-28 | Fonds De Dev Des Filieres Des Oleagineux Et Proteagineux Fidop | Utilisation d'ethers de glycerol comme activateurs des effets herbicides d'une substance herbicide |
| EP2305030A1 (de) | 2009-09-14 | 2011-04-06 | Bayer CropScience AG | Alkylpolypropylenglycolpolyethylenglycol enthaltende agrochemische Zusammensetzungen |
| KR20130039331A (ko) * | 2010-06-29 | 2013-04-19 | 바이엘 인텔렉쳐 프로퍼티 게엠베하 | 사이클릭 카보닐아미딘을 포함하는 개량된 살충성 조성물 |
| EP2457890A1 (en) * | 2010-11-29 | 2012-05-30 | Cognis IP Management GmbH | Biocide compositions comprising alkoxylation products of isoamyl alcohol derivatives |
| US20120210452A1 (en) * | 2011-02-16 | 2012-08-16 | Fashion Chemicals, Gmbh & Co Kg | Alkoxylated non-ionic alkanol adjuvant formulations and methods for making and using the same |
| TWI634840B (zh) * | 2011-03-31 | 2018-09-11 | 先正達合夥公司 | 植物生長調節組成物及使用其之方法 |
| ES2756799T3 (es) | 2011-04-20 | 2020-04-27 | Huntsman Petrochemical Llc | Uso de agentes de reducción de deriva de la pulverización que comprenden tensioactivos de bajo equilibrio hidrófilo-lipófilo |
| PL2811828T3 (pl) * | 2012-01-23 | 2022-01-03 | Syngenta Participations Ag | Kompozycje adiuwantowe |
| MY169208A (en) | 2012-04-24 | 2019-03-18 | Stepan Co | Unsaturated fatty alcohol alkoxylates from natural oil metathesis |
| EP2841541B1 (en) | 2012-04-24 | 2020-11-11 | Stepan Company | Unsaturated fatty alcohol derivatives from natural oil metathesis |
| US9591854B2 (en) | 2012-06-18 | 2017-03-14 | Basf Se | Agroformulations containing a lactone based alkoxylate |
| EP2894963B1 (en) * | 2012-09-13 | 2018-08-22 | Rhodia Operations | Wettable peat moss, method of preparation, and method of use |
| EP2877563B1 (en) * | 2012-09-29 | 2018-03-07 | Dow Global Technologies LLC | Alkoxylate compositions and their use as agricultural adjuvants |
| AU2013357590B2 (en) * | 2012-12-14 | 2017-02-02 | Basf Se | Composition comprising a pesticide and an alkoxylate of 2-isopropyl-5-methylhexane-1-amine |
| EP3099168B1 (en) * | 2014-01-30 | 2019-09-11 | Basf Se | Asymmetric formales and acetales as adjuvants for crop protection |
| BR112016025727B1 (pt) | 2014-05-06 | 2021-11-30 | Basf Se | Composição, métodos para preparar uma composição e para controlar fungos fitopatoênicos e/ou vegetação indesejável e/ou infestação indesejável, e, uso de um hidróxialquil polioxileno glicol éter |
| EP3151664A4 (en) * | 2014-06-06 | 2017-12-20 | Archer Daniels Midland Company | Microemulsions and uses thereof |
| UA118991C2 (uk) * | 2014-09-16 | 2019-04-10 | Басф Се | Агрохімічний суспензійний концентрат, що включає алкоксильований спирт, розчинений у водній фазі |
| BR112017016841B1 (pt) | 2015-02-10 | 2022-06-07 | Basf Se | Composição, método para preparar a composição, método para controlar fungos fitopatogênicos e/ou vegetação e/ou infestação de inseto indesejável ou ácaro indesejável e/ou para regular o crescimento de plantas, semente, e, uso de um éster alcoxilado. |
| PL3636691T3 (pl) | 2015-10-07 | 2021-09-27 | Elementis Specialties, Inc. | Środek zwilżający i przeciwpieniący |
| EA201891107A1 (ru) | 2015-11-06 | 2018-12-28 | Басф Се | Новые способы отделения воды от водных систем |
| AU2016368473A1 (en) * | 2015-12-09 | 2018-06-07 | Akzo Nobel Chemicals International B.V. | Low foaming high electrolyte compositions |
| BR112019016058B1 (pt) | 2017-02-03 | 2022-12-13 | Basf Se | Método para intensificar a infiltração de água no solo e uso de uma composição |
| CN110612333B (zh) | 2017-05-10 | 2022-05-24 | 巴斯夫欧洲公司 | 具有支化结构的聚合物 |
| AU2018336770B2 (en) * | 2017-09-20 | 2024-02-01 | Basf Se | Treated medium for plant growth that has increased water retention |
| WO2019185610A1 (en) | 2018-03-26 | 2019-10-03 | Basf Se | Method of reducing soil water repellency |
| WO2019185612A1 (en) | 2018-03-26 | 2019-10-03 | Basf Se | Method of reducing soil water repellency |
| UA128582C2 (uk) * | 2018-07-30 | 2024-08-21 | Байєр Акцієнгезелльшафт | Гербіцидні композиції з поліпшеними властивостями |
| WO2020123130A1 (en) * | 2018-12-11 | 2020-06-18 | Dow Global Technologies Llc | Aqueous solutions of poorly soluble pesticides using polyalkyoxylated alcohols |
| CN114080155B (zh) * | 2019-07-11 | 2024-03-26 | 巴斯夫欧洲公司 | 用于喷洒漂移控制的剪切稳定组合物 |
| EP4521927A1 (en) * | 2022-05-11 | 2025-03-19 | Adama Makhteshim Ltd. | Phthalimide fungicide composition |
| EP4338592A1 (en) | 2022-09-15 | 2024-03-20 | Basf Se | Use of compound for improving the efficacy of herbicides |
| CN120380059A (zh) * | 2022-12-29 | 2025-07-25 | 迈图高新材料公司 | 佐剂组合物及使用其处理植物的方法 |
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| EP2271697B1 (de) | 2008-04-24 | 2014-07-09 | Basf Se | Alkoholalkoxylate, diese enthaltende mittel und verwendung der alkoholalkoxylate als adjuvans für den agrochemischen bereich |
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2003
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- 2003-04-24 US US10/512,422 patent/US8129312B2/en active Active
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- 2003-04-24 CA CA2697544A patent/CA2697544C/en not_active Expired - Fee Related
- 2003-04-24 EP EP03747121A patent/EP1501355B1/de not_active Expired - Lifetime
- 2003-04-24 WO PCT/EP2003/004276 patent/WO2003090531A1/de not_active Ceased
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- 2003-04-24 AT AT03747121T patent/ATE468016T1/de active
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- 2003-04-24 DE DE50312724T patent/DE50312724D1/de not_active Expired - Lifetime
- 2003-04-24 ES ES03747121T patent/ES2345980T3/es not_active Expired - Lifetime
- 2003-04-24 EA EA200900076A patent/EA015423B1/ru not_active IP Right Cessation
- 2003-04-24 PL PL373335A patent/PL211208B1/pl unknown
- 2003-04-24 PT PT03747121T patent/PT1501355E/pt unknown
- 2003-04-24 CA CA2482758A patent/CA2482758C/en not_active Expired - Lifetime
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2004
- 2004-10-12 IL IL164524A patent/IL164524A/en active IP Right Grant
- 2004-10-20 IN IN2386CH2004 patent/IN2004CH02386A/en unknown
- 2004-11-23 ZA ZA200409411A patent/ZA200409411B/en unknown
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2009
- 2009-05-26 IL IL198972A patent/IL198972A/en active IP Right Grant
- 2009-11-25 AU AU2009240808A patent/AU2009240808B2/en not_active Ceased
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2010
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