ES2237198T3 - Formulaciones plaguicidas que contienen tensioactivos de ester hemisulfato de triestiril-fenol alcoxilado neutralizado con amina alcoxilada. - Google Patents
Formulaciones plaguicidas que contienen tensioactivos de ester hemisulfato de triestiril-fenol alcoxilado neutralizado con amina alcoxilada.Info
- Publication number
- ES2237198T3 ES2237198T3 ES99965455T ES99965455T ES2237198T3 ES 2237198 T3 ES2237198 T3 ES 2237198T3 ES 99965455 T ES99965455 T ES 99965455T ES 99965455 T ES99965455 T ES 99965455T ES 2237198 T3 ES2237198 T3 ES 2237198T3
- Authority
- ES
- Spain
- Prior art keywords
- surfactant
- formula
- composition
- inclusive
- alkyl
- 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.)
- Expired - Lifetime
Links
- 239000000203 mixture Substances 0.000 title claims description 81
- 150000001412 amines Chemical class 0.000 title claims description 40
- 150000002148 esters Chemical class 0.000 title description 11
- 150000001875 compounds Chemical class 0.000 claims abstract description 28
- 150000001768 cations Chemical class 0.000 claims abstract description 4
- 239000004094 surface-active agent Substances 0.000 claims description 83
- 238000009472 formulation Methods 0.000 claims description 32
- 238000000034 method Methods 0.000 claims description 17
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 15
- -1 n-octadecyl Chemical group 0.000 claims description 13
- 125000000217 alkyl group Chemical group 0.000 claims description 12
- 239000003090 pesticide formulation Substances 0.000 claims description 10
- MXWJVTOOROXGIU-UHFFFAOYSA-N atrazine Chemical group CCNC1=NC(Cl)=NC(NC(C)C)=N1 MXWJVTOOROXGIU-UHFFFAOYSA-N 0.000 claims description 8
- 229910052799 carbon Inorganic materials 0.000 claims description 7
- 238000002360 preparation method Methods 0.000 claims description 4
- 230000008569 process Effects 0.000 claims description 4
- 239000000575 pesticide Substances 0.000 claims description 3
- 239000005562 Glyphosate Substances 0.000 claims 1
- XDDAORKBJWWYJS-UHFFFAOYSA-N glyphosate Chemical compound OC(=O)CNCP(O)(O)=O XDDAORKBJWWYJS-UHFFFAOYSA-N 0.000 claims 1
- 229940097068 glyphosate Drugs 0.000 claims 1
- 230000003993 interaction Effects 0.000 claims 1
- 238000006386 neutralization reaction Methods 0.000 claims 1
- 125000006686 (C1-C24) alkyl group Chemical group 0.000 abstract 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000002253 acid Substances 0.000 description 10
- 239000000047 product Substances 0.000 description 10
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 9
- 239000003760 tallow Substances 0.000 description 8
- 239000004480 active ingredient Substances 0.000 description 7
- 229920001400 block copolymer Chemical class 0.000 description 6
- 239000012141 concentrate Substances 0.000 description 6
- 239000007788 liquid Substances 0.000 description 6
- WVQBLGZPHOPPFO-UHFFFAOYSA-N 2-chloro-N-(2-ethyl-6-methylphenyl)-N-(1-methoxypropan-2-yl)acetamide Chemical compound CCC1=CC=CC(C)=C1N(C(C)COC)C(=O)CCl WVQBLGZPHOPPFO-UHFFFAOYSA-N 0.000 description 5
- PFJJMJDEVDLPNE-UHFFFAOYSA-N Benoxacor Chemical compound C1=CC=C2N(C(=O)C(Cl)Cl)C(C)COC2=C1 PFJJMJDEVDLPNE-UHFFFAOYSA-N 0.000 description 5
- RVGRUAULSDPKGF-UHFFFAOYSA-N Poloxamer Chemical compound C1CO1.CC1CO1 RVGRUAULSDPKGF-UHFFFAOYSA-N 0.000 description 5
- 159000000032 aromatic acids Chemical class 0.000 description 5
- 239000000463 material Substances 0.000 description 5
- 238000002156 mixing Methods 0.000 description 5
- 239000000126 substance Substances 0.000 description 5
- 239000000725 suspension Substances 0.000 description 5
- WVQBLGZPHOPPFO-LBPRGKRZSA-N (S)-metolachlor Chemical compound CCC1=CC=CC(C)=C1N([C@@H](C)COC)C(=O)CCl WVQBLGZPHOPPFO-LBPRGKRZSA-N 0.000 description 4
- XFRVVPUIAFSTFO-UHFFFAOYSA-N 1-Tridecanol Chemical compound CCCCCCCCCCCCCO XFRVVPUIAFSTFO-UHFFFAOYSA-N 0.000 description 4
- 238000006243 chemical reaction Methods 0.000 description 4
- 239000003795 chemical substances by application Substances 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 239000007787 solid Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 230000003068 static effect Effects 0.000 description 4
- 238000003756 stirring Methods 0.000 description 4
- 229940087291 tridecyl alcohol Drugs 0.000 description 4
- 239000005617 S-Metolachlor Substances 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 230000009918 complex formation Effects 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000004495 emulsifiable concentrate Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 239000012530 fluid Substances 0.000 description 3
- 239000008187 granular material Substances 0.000 description 3
- 239000004009 herbicide Substances 0.000 description 3
- 230000003301 hydrolyzing effect Effects 0.000 description 3
- 239000003921 oil Substances 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 229920005682 EO-PO block copolymer Polymers 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- 239000002518 antifoaming agent Substances 0.000 description 2
- 239000007900 aqueous suspension Substances 0.000 description 2
- 230000002599 biostatic effect Effects 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 description 2
- 230000002363 herbicidal effect Effects 0.000 description 2
- 150000002430 hydrocarbons Chemical group 0.000 description 2
- 239000002245 particle Substances 0.000 description 2
- 150000002989 phenols Chemical class 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000007858 starting material Substances 0.000 description 2
- 230000009469 supplementation Effects 0.000 description 2
- 239000004546 suspension concentrate Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 239000002562 thickening agent Substances 0.000 description 2
- 239000004563 wettable powder Substances 0.000 description 2
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- 239000004215 Carbon black (E152) Substances 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 241001272567 Hominoidea Species 0.000 description 1
- 229910021607 Silver chloride Inorganic materials 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 230000007059 acute toxicity Effects 0.000 description 1
- 231100000403 acute toxicity Toxicity 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000000996 additive effect Effects 0.000 description 1
- 239000003905 agrochemical Substances 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 239000001166 ammonium sulphate Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000000729 antidote Substances 0.000 description 1
- 229940075522 antidotes Drugs 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000003556 assay Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- SMLHHBQGIJMAIM-UHFFFAOYSA-N calcium;2-dodecylbenzenesulfonic acid Chemical compound [Ca].CCCCCCCCCCCCC1=CC=CC=C1S(O)(=O)=O SMLHHBQGIJMAIM-UHFFFAOYSA-N 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- 238000003776 cleavage reaction Methods 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 238000007727 cost benefit analysis Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical group OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 1
- 239000012895 dilution Substances 0.000 description 1
- 238000010790 dilution Methods 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 230000001804 emulsifying effect Effects 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 238000005065 mining Methods 0.000 description 1
- 230000003472 neutralizing effect Effects 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 229920000642 polymer Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 230000009467 reduction Effects 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 238000007127 saponification reaction Methods 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000007017 scission Effects 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- HKZLPVFGJNLROG-UHFFFAOYSA-M silver monochloride Chemical compound [Cl-].[Ag+] HKZLPVFGJNLROG-UHFFFAOYSA-M 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000002123 temporal effect Effects 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 238000005809 transesterification reaction Methods 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
- 239000003981 vehicle Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/32—Polymers modified by chemical after-treatment
- C08G65/329—Polymers modified by chemical after-treatment with organic compounds
- C08G65/333—Polymers modified by chemical after-treatment with organic compounds containing nitrogen
- C08G65/33303—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group
- C08G65/33306—Polymers modified by chemical after-treatment with organic compounds containing nitrogen containing amino group acyclic
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C305/00—Esters of sulfuric acids
- C07C305/02—Esters of sulfuric acids having oxygen atoms of sulfate groups bound to acyclic carbon atoms of a carbon skeleton
- C07C305/04—Esters of sulfuric acids having oxygen atoms of sulfate groups bound to acyclic carbon atoms of a carbon skeleton being acyclic and saturated
- C07C305/10—Esters of sulfuric acids having oxygen atoms of sulfate groups bound to acyclic carbon atoms of a carbon skeleton being acyclic and saturated being further substituted by singly-bound oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G65/00—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule
- C08G65/02—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring
- C08G65/26—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds
- C08G65/2603—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen
- C08G65/2606—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups
- C08G65/2612—Macromolecular compounds obtained by reactions forming an ether link in the main chain of the macromolecule from cyclic ethers by opening of the heterocyclic ring from cyclic ethers and other compounds the other compounds containing oxygen containing hydroxyl groups containing aromatic or arylaliphatic hydroxyl groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
- C08L71/02—Polyalkylene oxides
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Plant Pathology (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- Engineering & Computer Science (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- General Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US21106298A | 1998-12-14 | 1998-12-14 | |
| US211062 | 1998-12-14 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2237198T3 true ES2237198T3 (es) | 2005-07-16 |
Family
ID=22785452
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES99965455T Expired - Lifetime ES2237198T3 (es) | 1998-12-14 | 1999-12-13 | Formulaciones plaguicidas que contienen tensioactivos de ester hemisulfato de triestiril-fenol alcoxilado neutralizado con amina alcoxilada. |
Country Status (30)
Families Citing this family (22)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2003022049A1 (en) | 2001-09-07 | 2003-03-20 | Syngenta Participations Ag | Surfactant systems for agriculturally active compounds |
| US20050159625A1 (en) * | 2004-01-19 | 2005-07-21 | Coates John S. | Alkoxylated amine and process therefor |
| UA96128C2 (ru) * | 2005-06-30 | 2011-10-10 | Сингента Партисипейшнс Аг | Способы обработки семян, композиция для обработки семян, водное пестицидное средство в виде суспензии, способ защиты семян и органов растений и семян |
| CN101541167A (zh) * | 2006-11-22 | 2009-09-23 | 巴斯夫欧洲公司 | 基于水的液体农业化学配制剂 |
| KR101084454B1 (ko) * | 2007-05-16 | 2011-11-21 | 가부시끼가이샤 도꾸야마 | 포토레지스트 현상액 |
| ES2324809B1 (es) * | 2008-02-13 | 2010-05-28 | Consejo Superior De Investigaciones Cientificas | Formulaciones de liberacion lenta de plaguicidas respetuosas con el medioambiente. |
| HRP20130908T1 (hr) * | 2008-03-25 | 2013-10-25 | Syngenta Participations Ag | Pripravci surfaktanata |
| TWI513404B (zh) * | 2009-05-08 | 2015-12-21 | Croda Inc | 農化調配物之界面活性劑 |
| BR112012005440A2 (pt) * | 2009-09-10 | 2016-04-12 | Univ Texas | composição para tratar uma formação possuindo hidrocarboneto, e, métodos para preparar uma composição, e para tratar uma formação possuindo hidrocarboneto para recuperar petróleo |
| WO2011094442A1 (en) * | 2010-01-28 | 2011-08-04 | Board Of Regents, The University Of Texas System | Styrylphenol alkoxylate sulfate as a new surfactant composition for enhanced oil recovery applications |
| CA2810384C (en) | 2010-09-14 | 2019-08-27 | Basf Se | Composition containing a pyripyropene insecticide and an adjuvant |
| KR101938020B1 (ko) * | 2010-09-14 | 2019-01-11 | 바스프 에스이 | 피리피로펜 살곤충제 및 염기를 함유하는 조성물 |
| CN102504233B (zh) * | 2011-11-02 | 2013-05-29 | 浙江皇马科技股份有限公司 | 一种三苯乙烯苯酚聚氧乙烯醚油酸酯的制备方法 |
| KR102056608B1 (ko) | 2012-03-12 | 2019-12-17 | 바스프 에스이 | 피리피로펜 살곤충제의 수성 현탁액 농축물 제형의 제조 방법 |
| MX360698B (es) | 2012-03-12 | 2018-11-14 | Basf Se | Formulación concentrada líquida que contiene un insecticida de piripiropeno i. |
| US9924712B2 (en) | 2012-03-12 | 2018-03-27 | Basf Se | Liquid concentrate formulation containing a pyripyropene insecticide II |
| EP2855406A4 (en) | 2012-05-31 | 2016-01-06 | Exxonmobil Chem Patents Inc | REMOVAL OF STYRENE IN A PROCESS FOR RECOVERING PARAXYLENE |
| JP5960349B2 (ja) * | 2012-08-08 | 2016-08-02 | 日華化学株式会社 | ポリエステル繊維用染色助剤、並びにこれを用いたポリエステル繊維の染色方法及び染色物の製造方法 |
| US10029967B2 (en) | 2014-03-18 | 2018-07-24 | Rhodia Operations | Tri-substituted aromatic-containing monomers, copolymers and methods for use |
| CN104084086B (zh) * | 2014-07-17 | 2016-01-13 | 天津悦泰石化科技有限公司 | 用于车用尿素溶液的表面活性剂及其制备方法和用途 |
| WO2022013702A1 (en) * | 2020-07-11 | 2022-01-20 | Upl Limited | A solid agrochemical composition and process of preparation thereof |
| CN113424832B (zh) * | 2021-07-02 | 2022-11-08 | 中化化工科学技术研究总院有限公司 | 一种吡蚜酮·呋虫胺干悬浮剂及其制备方法 |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6183267A (ja) * | 1984-10-01 | 1986-04-26 | Toray Ind Inc | インクジェット染色法 |
| FR2673075B1 (fr) * | 1991-02-22 | 1998-12-31 | Rhone Poulenc Chimie | Microemulsions de pyrethrouides et leur utilisation. |
| TW224421B (GUID-C5D7CC26-194C-43D0-91A1-9AE8C70A9BFF.html) * | 1991-12-24 | 1994-06-01 | Shell Internat Researce Schappel N V | |
| RU2024502C1 (ru) * | 1992-01-30 | 1994-12-15 | Уфимское производственное объединение "Химпром" | Способ получения лаурилсульфата магния |
| RU2064475C1 (ru) * | 1992-10-29 | 1996-07-27 | Игорь Александрович Ямсков | Ацетилсалицилат[трис(гидроксметил)метил]аммония, обладающий противовоспалительной, анальгетической, жаропонижающей и антиагрегантной активностью |
| DE4343856A1 (de) * | 1993-12-22 | 1995-06-29 | Hoechst Ag | Öl-in-Wasser-Emulsionen |
| US5674517A (en) * | 1996-04-26 | 1997-10-07 | Henkel Corporation | Emulsifier for pesticide concentrates |
-
1999
- 1999-12-06 CR CR6136A patent/CR6136A/xx not_active Application Discontinuation
- 1999-12-09 CO CO99077084A patent/CO5210927A1/es active IP Right Grant
- 1999-12-09 GT GT199900211A patent/GT199900211A/es unknown
- 1999-12-13 CN CNB998144452A patent/CN1213023C/zh not_active Expired - Fee Related
- 1999-12-13 HU HU0104753A patent/HU229246B1/hu not_active IP Right Cessation
- 1999-12-13 WO PCT/EP1999/009869 patent/WO2000035863A1/en active IP Right Grant
- 1999-12-13 BR BRPI9916198-2A patent/BR9916198B1/pt not_active IP Right Cessation
- 1999-12-13 ES ES99965455T patent/ES2237198T3/es not_active Expired - Lifetime
- 1999-12-13 PT PT99965455T patent/PT1140808E/pt unknown
- 1999-12-13 IL IL14338999A patent/IL143389A0/xx active IP Right Grant
- 1999-12-13 MY MYPI99005412A patent/MY117825A/en unknown
- 1999-12-13 UA UA2001074952A patent/UA69429C2/uk unknown
- 1999-12-13 AR ARP990106329A patent/AR021640A1/es active IP Right Grant
- 1999-12-13 NZ NZ511942A patent/NZ511942A/xx not_active IP Right Cessation
- 1999-12-13 DE DE69923868T patent/DE69923868T2/de not_active Expired - Lifetime
- 1999-12-13 AT AT99965455T patent/ATE289589T1/de active
- 1999-12-13 CZ CZ20012086A patent/CZ302156B6/cs not_active IP Right Cessation
- 1999-12-13 ID IDW00200101187A patent/ID29349A/id unknown
- 1999-12-13 AU AU20964/00A patent/AU750616B2/en not_active Ceased
- 1999-12-13 KR KR1020017007361A patent/KR100688922B1/ko not_active Expired - Fee Related
- 1999-12-13 TR TR2001/01646T patent/TR200101646T2/xx unknown
- 1999-12-13 PL PL348231A patent/PL199067B1/pl unknown
- 1999-12-13 JP JP2000588125A patent/JP4402300B2/ja not_active Expired - Fee Related
- 1999-12-13 CA CA002352360A patent/CA2352360C/en not_active Expired - Fee Related
- 1999-12-13 EP EP99965455A patent/EP1140808B1/en not_active Expired - Lifetime
- 1999-12-13 EG EG158599A patent/EG22461A/xx active
- 1999-12-13 RU RU2001118824/04A patent/RU2241699C2/ru not_active IP Right Cessation
- 1999-12-14 TW TW88121862A patent/TW575546B/zh not_active IP Right Cessation
-
2001
- 2001-05-24 IL IL143389A patent/IL143389A/en not_active IP Right Cessation
- 2001-06-07 ZA ZA200104654A patent/ZA200104654B/xx unknown
- 2001-06-14 US US09/881,414 patent/US6495595B2/en not_active Expired - Lifetime
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