KR20130121908A - 이소아밀 알코올 유도체의 알콕시화 생성물을 포함하는 살생물제 조성물 - Google Patents
이소아밀 알코올 유도체의 알콕시화 생성물을 포함하는 살생물제 조성물 Download PDFInfo
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- KR20130121908A KR20130121908A KR1020137017068A KR20137017068A KR20130121908A KR 20130121908 A KR20130121908 A KR 20130121908A KR 1020137017068 A KR1020137017068 A KR 1020137017068A KR 20137017068 A KR20137017068 A KR 20137017068A KR 20130121908 A KR20130121908 A KR 20130121908A
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- Prior art keywords
- alcohols
- esters
- branched
- methyl
- linear
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- 239000003549 soybean oil Substances 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- PUYXTUJWRLOUCW-UHFFFAOYSA-N spiroxamine Chemical compound O1C(CN(CC)CCC)COC11CCC(C(C)(C)C)CC1 PUYXTUJWRLOUCW-UHFFFAOYSA-N 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 229940094908 stearyl myristate Drugs 0.000 description 1
- 230000005082 stem growth Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 210000002784 stomach Anatomy 0.000 description 1
- 229960005322 streptomycin Drugs 0.000 description 1
- 150000003890 succinate salts Chemical class 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
- IIACRCGMVDHOTQ-UHFFFAOYSA-N sulfamic acid Chemical compound NS(O)(=O)=O IIACRCGMVDHOTQ-UHFFFAOYSA-N 0.000 description 1
- NVBFHJWHLNUMCV-UHFFFAOYSA-N sulfamide Chemical class NS(N)(=O)=O NVBFHJWHLNUMCV-UHFFFAOYSA-N 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000013589 supplement Substances 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- 229960003080 taurine Drugs 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
- 229960002180 tetracycline Drugs 0.000 description 1
- 229930101283 tetracycline Natural products 0.000 description 1
- 235000019364 tetracycline Nutrition 0.000 description 1
- 150000003522 tetracyclines Chemical class 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
- HBPNTDBLHQHPLH-UHFFFAOYSA-N tetradecyl 16-methylheptadecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C HBPNTDBLHQHPLH-UHFFFAOYSA-N 0.000 description 1
- AVKVDDQTHIQFSC-UHFFFAOYSA-N tetradecyl docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC AVKVDDQTHIQFSC-UHFFFAOYSA-N 0.000 description 1
- DHZWALZKPWZSMA-UHFFFAOYSA-N tetradecyl oleate Natural products CCCCCCCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC DHZWALZKPWZSMA-UHFFFAOYSA-N 0.000 description 1
- DZKXJUASMGQEMA-UHFFFAOYSA-N tetradecyl tetradecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCC DZKXJUASMGQEMA-UHFFFAOYSA-N 0.000 description 1
- 229960005199 tetramethrin Drugs 0.000 description 1
- NWWZPOKUUAIXIW-FLIBITNWSA-N thiamethoxam Chemical compound [O-][N+](=O)\N=C/1N(C)COCN\1CC1=CN=C(Cl)S1 NWWZPOKUUAIXIW-FLIBITNWSA-N 0.000 description 1
- 150000003558 thiocarbamic acid derivatives Chemical class 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
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- DENPQNAWGQXKCU-UHFFFAOYSA-N thiophene-2-carboxamide Chemical class NC(=O)C1=CC=CS1 DENPQNAWGQXKCU-UHFFFAOYSA-N 0.000 description 1
- 229960002447 thiram Drugs 0.000 description 1
- KUAZQDVKQLNFPE-UHFFFAOYSA-N thiram Chemical compound CN(C)C(=S)SSC(=S)N(C)C KUAZQDVKQLNFPE-UHFFFAOYSA-N 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- OBZIQQJJIKNWNO-UHFFFAOYSA-N tolclofos-methyl Chemical compound COP(=S)(OC)OC1=C(Cl)C=C(C)C=C1Cl OBZIQQJJIKNWNO-UHFFFAOYSA-N 0.000 description 1
- 231100000816 toxic dose Toxicity 0.000 description 1
- 231100000027 toxicology Toxicity 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
- 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
- 238000013519 translation Methods 0.000 description 1
- BAZVSMNPJJMILC-UHFFFAOYSA-N triadimenol Chemical compound C1=NC=NN1C(C(O)C(C)(C)C)OC1=CC=C(Cl)C=C1 BAZVSMNPJJMILC-UHFFFAOYSA-N 0.000 description 1
- 150000003918 triazines Chemical class 0.000 description 1
- 150000003852 triazoles Chemical class 0.000 description 1
- IQGKIPDJXCAMSM-UHFFFAOYSA-N triazoxide Chemical compound N=1C2=CC=C(Cl)C=C2[N+]([O-])=NC=1N1C=CN=C1 IQGKIPDJXCAMSM-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
- ZOKXUAHZSKEQSS-UHFFFAOYSA-N tribufos Chemical compound CCCCSP(=O)(SCCCC)SCCCC ZOKXUAHZSKEQSS-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
- DQJCHOQLCLEDLL-UHFFFAOYSA-N tricyclazole Chemical compound CC1=CC=CC2=C1N1C=NN=C1S2 DQJCHOQLCLEDLL-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
- 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
- 229940057402 undecyl alcohol Drugs 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- JARYYMUOCXVXNK-IMTORBKUSA-N validamycin 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-IMTORBKUSA-N 0.000 description 1
- MYPYJXKWCTUITO-LYRMYLQWSA-N vancomycin Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C(O)=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)NC)[C@H]1C[C@](C)(N)[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-N 0.000 description 1
- 229960003165 vancomycin Drugs 0.000 description 1
- MYPYJXKWCTUITO-UHFFFAOYSA-N vancomycin Natural products O1C(C(=C2)Cl)=CC=C2C(O)C(C(NC(C2=CC(O)=CC(O)=C2C=2C(O)=CC=C3C=2)C(O)=O)=O)NC(=O)C3NC(=O)C2NC(=O)C(CC(N)=O)NC(=O)C(NC(=O)C(CC(C)C)NC)C(O)C(C=C3Cl)=CC=C3OC3=CC2=CC1=C3OC1OC(CO)C(O)C(O)C1OC1CC(C)(N)C(O)C(C)O1 MYPYJXKWCTUITO-UHFFFAOYSA-N 0.000 description 1
- 230000017260 vegetative to reproductive phase transition of meristem Effects 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- FJBGIXKIXPUXBY-UHFFFAOYSA-N {2-[3-(4-chlorophenyl)propyl]-2,4,4-trimethyl-1,3-oxazolidin-3-yl}(imidazol-1-yl)methanone Chemical compound C1=CN=CN1C(=O)N1C(C)(C)COC1(C)CCCC1=CC=C(Cl)C=C1 FJBGIXKIXPUXBY-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D303/00—Compounds containing three-membered rings having one oxygen atom as the only ring hetero atom
- C07D303/02—Compounds containing oxirane rings
- C07D303/04—Compounds containing oxirane rings containing only hydrogen and carbon atoms in addition to the ring oxygen atoms
-
- 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
- A01N25/30—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
- C07C41/00—Preparation of ethers; Preparation of compounds having groups, groups or groups
- C07C41/01—Preparation of ethers
- C07C41/02—Preparation of ethers from oxiranes
- C07C41/03—Preparation of ethers from oxiranes by reaction of oxirane rings with hydroxy groups
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C43/00—Ethers; Compounds having groups, groups or groups
- C07C43/02—Ethers
- C07C43/03—Ethers having all ether-oxygen atoms bound to acyclic carbon atoms
- C07C43/04—Saturated ethers
- C07C43/10—Saturated ethers of polyhydroxy compounds
- C07C43/11—Polyethers containing —O—(C—C—O—)n units with ≤ 2 n≤ 10
-
- 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
- C08G65/331—Polymers modified by chemical after-treatment with organic compounds containing oxygen
- C08G65/3311—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing a hydroxy group
- C08G65/3312—Polymers modified by chemical after-treatment with organic compounds containing oxygen containing a hydroxy group acyclic
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K23/00—Use of substances as emulsifying, wetting, dispersing, or foam-producing agents
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Agronomy & Crop Science (AREA)
- Zoology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Toxicology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Materials Engineering (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP10192858.8 | 2010-11-29 | ||
| EP10192858A EP2457890A1 (en) | 2010-11-29 | 2010-11-29 | Biocide compositions comprising alkoxylation products of isoamyl alcohol derivatives |
| PCT/EP2011/069799 WO2012072393A1 (en) | 2010-11-29 | 2011-11-10 | Biocide compositions comprising alkoxylation products of isoamyl alcohol derivates |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20130121908A true KR20130121908A (ko) | 2013-11-06 |
Family
ID=43726107
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020137017068A Withdrawn KR20130121908A (ko) | 2010-11-29 | 2011-11-10 | 이소아밀 알코올 유도체의 알콕시화 생성물을 포함하는 살생물제 조성물 |
Country Status (13)
| Country | Link |
|---|---|
| US (1) | US9497960B2 (enExample) |
| EP (1) | EP2457890A1 (enExample) |
| JP (1) | JP5881724B2 (enExample) |
| KR (1) | KR20130121908A (enExample) |
| CN (1) | CN103221371B (enExample) |
| AR (1) | AR083965A1 (enExample) |
| AU (1) | AU2011335285B2 (enExample) |
| BR (1) | BR112013012888A2 (enExample) |
| MX (1) | MX2013005981A (enExample) |
| RU (1) | RU2013129608A (enExample) |
| SG (1) | SG190225A1 (enExample) |
| WO (1) | WO2012072393A1 (enExample) |
| ZA (1) | ZA201304775B (enExample) |
Families Citing this family (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| ES2644129T3 (es) * | 2012-05-10 | 2017-11-27 | Basf Se | Alcoholes alcoxilados y su uso en formulaciones para la limpieza de superficies duras |
| US20130303430A1 (en) * | 2012-05-10 | 2013-11-14 | Basf Se | Alkoxylated alcohols and their use in formulations for hard surface cleaning |
| UA123769C2 (uk) * | 2015-06-04 | 2021-06-02 | АРІСТА ЛАЙФСАЙЄНС НОРТ АМЕРІКА, ЕлЕлСі | Стабілізовані поверхнево-активною речовиною препарати оксиму циклогександіоксиду |
| PL3636691T3 (pl) | 2015-10-07 | 2021-09-27 | Elementis Specialties, Inc. | Środek zwilżający i przeciwpieniący |
| AU2016368473A1 (en) | 2015-12-09 | 2018-06-07 | Akzo Nobel Chemicals International B.V. | Low foaming high electrolyte compositions |
| CN106732714B (zh) * | 2016-11-25 | 2018-02-13 | 赣南师范大学 | 茚虫威中间体合成用催化剂及其制备方法 |
| JP7009405B2 (ja) * | 2018-02-26 | 2022-02-10 | 三洋化成工業株式会社 | 水面浮遊型農薬製剤用拡展剤及び農薬製剤 |
| KR20240089622A (ko) * | 2021-10-12 | 2024-06-20 | 헌츠만 페트로케미칼 엘엘씨 | 알콕시화된 에테르 아민의 제조 방법 및 이의 용도 |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3039770A1 (de) * | 1980-10-22 | 1982-05-27 | Basf Ag, 6700 Ludwigshafen | Verwendung von alkoxylierten verbindungen als nichtionische emulgatorkomponente in pflanzenschutzmittelformulierungen |
| FR2729307B1 (fr) * | 1995-01-18 | 1997-04-18 | Seppic Sa | Utilisation d'esters d'acides gras ethoxyles comme composants auto-emulsionnables notamment utiles pour la preparation de produits de traitement phytosanitaires ou de medicaments a usage veterinaire ou humain |
| AU696607B2 (en) * | 1995-06-16 | 1998-09-17 | Monsanto Company | Surfactants providing enhanced efficacy and/or rainfastness to pesticide formulations |
| JP2002128603A (ja) * | 2000-10-26 | 2002-05-09 | Takemoto Oil & Fat Co Ltd | 水面浮遊型農薬組成物用拡展剤及び水面浮遊型農薬組成物 |
| EP1210877A1 (en) * | 2000-12-01 | 2002-06-05 | Aventis CropScience GmbH | Oil-in-water emulsion formulation of insecticides |
| WO2003026416A2 (en) * | 2001-09-21 | 2003-04-03 | Cognis Corporation | Methods and compositions for use in agriculture |
| KR100983437B1 (ko) * | 2002-04-24 | 2010-09-20 | 바스프 에스이 | 농업기술 분야에서의 아쥬반트로서 특정 알콜알콕실레이트의 용도 |
| MY157730A (en) * | 2004-09-27 | 2016-07-15 | Kao Corp | Herbicide composition |
| US20070155644A1 (en) * | 2005-12-30 | 2007-07-05 | Archer-Daniel-Midland Company | Environmentally Friendly Solvent Containing Isoamyl Lactate |
| BRPI0602819B1 (pt) | 2006-06-26 | 2015-12-15 | Oxiteno S A Indústria E Comércio | composição agroquímica isenta de solventes aromáticos que possui caráter anticristalizante, tanto no produto formulado concentrado, quanto após sua diluição em água para o preparo da calda de pulverização |
| DE102006043444A1 (de) * | 2006-09-15 | 2008-03-27 | Bayer Cropscience Ag | Suspensionskonzentrate auf Ölbasis |
| TW201031743A (en) * | 2008-12-18 | 2010-09-01 | Basf Se | Surfactant mixture comprising branched short-chain and branched long-chain components |
| MX2011006618A (es) * | 2008-12-18 | 2011-07-12 | Akzo Nobel Nv | Composicion desespumante que comprende 2-propilheptanol alcoxilado. |
| US7981273B2 (en) | 2009-06-22 | 2011-07-19 | Uop Llc | Process for catalytic cracking of hydrocarbons using UZM-35 |
| ES2621807T3 (es) | 2009-11-06 | 2017-07-05 | Cognis Ip Management Gmbh | Procedimiento para la preparación de alcoholes de Guerbet |
-
2010
- 2010-11-29 EP EP10192858A patent/EP2457890A1/en not_active Withdrawn
-
2011
- 2011-11-10 RU RU2013129608/04A patent/RU2013129608A/ru not_active Application Discontinuation
- 2011-11-10 JP JP2013540297A patent/JP5881724B2/ja not_active Expired - Fee Related
- 2011-11-10 SG SG2013035803A patent/SG190225A1/en unknown
- 2011-11-10 AU AU2011335285A patent/AU2011335285B2/en not_active Ceased
- 2011-11-10 CN CN201180056012.0A patent/CN103221371B/zh not_active Expired - Fee Related
- 2011-11-10 WO PCT/EP2011/069799 patent/WO2012072393A1/en not_active Ceased
- 2011-11-10 MX MX2013005981A patent/MX2013005981A/es unknown
- 2011-11-10 KR KR1020137017068A patent/KR20130121908A/ko not_active Withdrawn
- 2011-11-10 US US13/990,340 patent/US9497960B2/en active Active
- 2011-11-10 BR BR112013012888A patent/BR112013012888A2/pt not_active Application Discontinuation
- 2011-11-23 AR ARP110104361A patent/AR083965A1/es active IP Right Grant
-
2013
- 2013-06-26 ZA ZA2013/04775A patent/ZA201304775B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| MX2013005981A (es) | 2013-07-22 |
| WO2012072393A1 (en) | 2012-06-07 |
| CN103221371B (zh) | 2016-02-24 |
| US20130252982A1 (en) | 2013-09-26 |
| RU2013129608A (ru) | 2015-01-10 |
| CN103221371A (zh) | 2013-07-24 |
| ZA201304775B (en) | 2014-09-25 |
| SG190225A1 (en) | 2013-06-28 |
| US9497960B2 (en) | 2016-11-22 |
| AR083965A1 (es) | 2013-04-10 |
| AU2011335285A1 (en) | 2013-06-13 |
| JP5881724B2 (ja) | 2016-03-09 |
| BR112013012888A2 (pt) | 2016-08-23 |
| EP2457890A1 (en) | 2012-05-30 |
| JP2013543876A (ja) | 2013-12-09 |
| AU2011335285B2 (en) | 2016-05-12 |
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