JP2005508392A - 分枝型反応生成物 - Google Patents
分枝型反応生成物 Download PDFInfo
- Publication number
- JP2005508392A JP2005508392A JP2003542316A JP2003542316A JP2005508392A JP 2005508392 A JP2005508392 A JP 2005508392A JP 2003542316 A JP2003542316 A JP 2003542316A JP 2003542316 A JP2003542316 A JP 2003542316A JP 2005508392 A JP2005508392 A JP 2005508392A
- Authority
- JP
- Japan
- Prior art keywords
- groups
- composition
- group
- aqueous
- compound
- 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.)
- Pending
Links
- 239000007795 chemical reaction product Substances 0.000 title claims description 10
- 239000000203 mixture Substances 0.000 claims abstract description 78
- 150000001875 compounds Chemical class 0.000 claims abstract description 59
- 125000002947 alkylene group Chemical group 0.000 claims abstract description 14
- -1 ethyleneoxy, 1,2-propyleneoxy Chemical group 0.000 claims abstract description 12
- 125000001183 hydrocarbyl group Chemical group 0.000 claims abstract description 12
- 229920006395 saturated elastomer Polymers 0.000 claims abstract description 8
- 125000000732 arylene group Chemical group 0.000 claims abstract description 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 claims abstract description 4
- 125000000962 organic group Chemical group 0.000 claims abstract description 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 3
- 239000001257 hydrogen Substances 0.000 claims abstract description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 39
- 239000004094 surface-active agent Substances 0.000 claims description 32
- 125000004432 carbon atom Chemical group C* 0.000 claims description 27
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 24
- 239000002518 antifoaming agent Substances 0.000 claims description 12
- 239000004816 latex Substances 0.000 claims description 10
- 229920000126 latex Polymers 0.000 claims description 10
- 239000000853 adhesive Substances 0.000 claims description 9
- 230000001070 adhesive effect Effects 0.000 claims description 9
- 239000000976 ink Substances 0.000 claims description 9
- 238000005555 metalworking Methods 0.000 claims description 9
- 239000003973 paint Substances 0.000 claims description 9
- 239000004593 Epoxy Substances 0.000 claims description 6
- 239000000047 product Substances 0.000 claims description 5
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 claims description 4
- 150000001412 amines Chemical class 0.000 claims description 3
- 125000000816 ethylene group Chemical group [H]C([H])([*:1])C([H])([H])[*:2] 0.000 claims description 3
- 229930195734 saturated hydrocarbon Natural products 0.000 claims description 3
- 229930195735 unsaturated hydrocarbon Natural products 0.000 claims description 3
- 125000000837 carbohydrate group Chemical group 0.000 claims description 2
- 125000002791 glucosyl group Chemical group C1([C@H](O)[C@@H](O)[C@H](O)[C@H](O1)CO)* 0.000 claims description 2
- 150000001336 alkenes Chemical class 0.000 claims 2
- 239000012190 activator Substances 0.000 claims 1
- 230000003254 anti-foaming effect Effects 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims 1
- 239000004711 α-olefin Substances 0.000 claims 1
- 239000000126 substance Substances 0.000 abstract description 6
- 238000006116 polymerization reaction Methods 0.000 description 14
- 239000006260 foam Substances 0.000 description 9
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 8
- 239000003795 chemical substances by application Substances 0.000 description 7
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 238000004140 cleaning Methods 0.000 description 6
- 238000005187 foaming Methods 0.000 description 5
- 150000004820 halides Chemical class 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 229910021529 ammonia Inorganic materials 0.000 description 4
- 230000000694 effects Effects 0.000 description 4
- 239000011541 reaction mixture Substances 0.000 description 4
- 239000006254 rheological additive Substances 0.000 description 4
- 239000002689 soil Substances 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 125000001424 substituent group Chemical group 0.000 description 4
- 239000012085 test solution Substances 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 150000004945 aromatic hydrocarbons Chemical group 0.000 description 3
- 229910052799 carbon Inorganic materials 0.000 description 3
- 239000002736 nonionic surfactant Substances 0.000 description 3
- 238000003756 stirring Methods 0.000 description 3
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 150000003973 alkyl amines Chemical class 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000003118 aryl group Chemical group 0.000 description 2
- 125000002837 carbocyclic group Chemical group 0.000 description 2
- 231100000584 environmental toxicity Toxicity 0.000 description 2
- 210000000497 foam cell Anatomy 0.000 description 2
- 125000005843 halogen group Chemical group 0.000 description 2
- 125000000623 heterocyclic group Chemical group 0.000 description 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 150000002924 oxiranes Chemical class 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 239000000376 reactant Substances 0.000 description 2
- 239000008234 soft water Substances 0.000 description 2
- 239000002023 wood Substances 0.000 description 2
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 description 1
- QBMRGCSVYXVPBI-UHFFFAOYSA-N 1-[2-[bis[2-(2-hydroxydecoxy)ethyl]amino]ethoxy]decan-2-ol Chemical compound CCCCCCCCC(O)COCCN(CCOCC(O)CCCCCCCC)CCOCC(O)CCCCCCCC QBMRGCSVYXVPBI-UHFFFAOYSA-N 0.000 description 1
- AAMHBRRZYSORSH-UHFFFAOYSA-N 2-octyloxirane Chemical compound CCCCCCCCC1CO1 AAMHBRRZYSORSH-UHFFFAOYSA-N 0.000 description 1
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 239000004908 Emulsion polymer Substances 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- 239000004677 Nylon Substances 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 125000003158 alcohol group Chemical group 0.000 description 1
- 125000005529 alkyleneoxy group Chemical group 0.000 description 1
- 125000000304 alkynyl group Chemical group 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 238000004364 calculation method Methods 0.000 description 1
- 150000001721 carbon Chemical group 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 230000003197 catalytic effect Effects 0.000 description 1
- 238000006757 chemical reactions by type Methods 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 239000003599 detergent Substances 0.000 description 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000003623 enhancer Substances 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 125000001033 ether group Chemical group 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 1
- 229930182470 glycoside Natural products 0.000 description 1
- 150000002338 glycosides Chemical class 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- 125000001165 hydrophobic group Chemical group 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 238000000199 molecular distillation Methods 0.000 description 1
- DIOQZVSQGTUSAI-UHFFFAOYSA-N n-butylhexane Natural products CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 239000002547 new drug Substances 0.000 description 1
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
- 229920001778 nylon Polymers 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000002572 peristaltic effect Effects 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 238000000518 rheometry Methods 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 125000004149 thio group Chemical group *S* 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Images
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/50—Ethers of hydroxy amines of undetermined structure, e.g. obtained by reactions of epoxides with hydroxy amines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/02—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C217/04—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated
- C07C217/28—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having etherified hydroxy groups and amino groups bound to acyclic carbon atoms of the same carbon skeleton the carbon skeleton being acyclic and saturated having one amino group and at least two singly-bound oxygen atoms, with at least one being part of an etherified hydroxy group, bound to the carbon skeleton, e.g. ethers of polyhydroxy amines
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/02—Emulsion paints including aerosols
- C09D5/024—Emulsion paints including aerosols characterised by the additives
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/002—Surface-active compounds containing sulfur
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D1/00—Detergent compositions based essentially on surface-active compounds; Use of these compounds as a detergent
- C11D1/38—Cationic compounds
- C11D1/42—Amino alcohols or amino ethers
- C11D1/44—Ethers of polyoxyalkylenes with amino alcohols; Condensation products of epoxyalkanes with amines
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Materials Engineering (AREA)
- Dispersion Chemistry (AREA)
- Crystallography & Structural Chemistry (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Detergent Compositions (AREA)
- Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
- Degasification And Air Bubble Elimination (AREA)
- Paints Or Removers (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Adhesives Or Adhesive Processes (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US33874301P | 2001-11-05 | 2001-11-05 | |
| US10/265,004 US7247606B2 (en) | 2001-11-05 | 2002-10-04 | Branched reaction products |
| PCT/US2002/034844 WO2003040277A2 (en) | 2001-11-05 | 2002-10-31 | Branched reaction products |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JP2005508392A true JP2005508392A (ja) | 2005-03-31 |
| JP2005508392A5 JP2005508392A5 (enExample) | 2006-01-05 |
Family
ID=26950891
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2003542316A Pending JP2005508392A (ja) | 2001-11-05 | 2002-10-31 | 分枝型反応生成物 |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US7247606B2 (enExample) |
| EP (1) | EP1441827B1 (enExample) |
| JP (1) | JP2005508392A (enExample) |
| AU (1) | AU2002363470A1 (enExample) |
| ES (1) | ES2404892T3 (enExample) |
| WO (1) | WO2003040277A2 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20090072182A1 (en) * | 2007-09-19 | 2009-03-19 | Baum's Flame Management, Llc | Fire fighting and cooling composition |
| PL2217639T3 (pl) * | 2007-11-09 | 2019-04-30 | Basf Se | Kompozycje do czyszczenia z alkoksylowanymi polialkanoloaminami |
| TW200936644A (en) * | 2007-11-09 | 2009-09-01 | Basf Se | Alkoxylated polyalkanolamines |
| US9212095B2 (en) | 2011-02-21 | 2015-12-15 | Construction Research & Technology, Gmbh | Use of HyperBranched polyether surfactant in cementitious systems |
| US10982046B2 (en) | 2014-07-10 | 2021-04-20 | Basf Se | Reaction products and use of same in defoamer compositions and methods for defoaming |
| US20210100177A1 (en) * | 2019-10-04 | 2021-04-08 | Milliken & Company | Horticulture Additive |
| US11891346B2 (en) | 2019-10-04 | 2024-02-06 | Milliken & Company | Horticulture additive |
Family Cites Families (32)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2355337A (en) * | 1942-08-28 | 1944-08-08 | Rohm & Haas | Preparation of ether amines |
| US2392158A (en) * | 1943-01-09 | 1946-01-01 | American Cyanamid Co | Oil soluble dyes |
| US2928877A (en) * | 1957-05-10 | 1960-03-15 | Wyandotte Chemicals Corp | Process for preparing oxyalkyleneamines |
| US3705139A (en) * | 1969-10-30 | 1972-12-05 | Lion Fat Oil Co Ltd | High molecular composition |
| FR2455570A1 (fr) * | 1979-05-03 | 1980-11-28 | Rhone Poulenc Ind | Procede de preparation de tris(ether-amines) et tris(ether-amines) ainsi obtenues |
| FR2489315A1 (fr) * | 1980-08-27 | 1982-03-05 | Rhone Poulenc Ind | Nouveaux aminoalcools polyoxaalkyles, leur procede de preparation et leur application comme agents de complexation de cations |
| FR2501676A1 (fr) * | 1981-03-11 | 1982-09-17 | Rhone Poulenc Spec Chim | Procede de n-alkylation de composes organiques azotes |
| US4438022A (en) * | 1982-07-30 | 1984-03-20 | Chevron Research Company | Lubricating oil compositions containing polyether polyamine ethanes |
| DE3504242A1 (de) * | 1985-02-08 | 1986-08-14 | Henkel KGaA, 4000 Düsseldorf | Verfahren zur herstellung von tertiaeren etheraminen |
| DE3614834A1 (de) * | 1986-05-02 | 1987-11-05 | Henkel Kgaa | Verwendung von aminogruppen enthaltenden polyglykolethern als schaumdrueckende zusaetze in schaumarmen reinigungsmitteln |
| DE3614825A1 (de) * | 1986-05-02 | 1987-11-05 | Henkel Kgaa | Verwendung von alkylaminopolyglykolethern als schaumdrueckende zusaetze in schaumarmen reinigungsmitteln |
| DE3737071A1 (de) * | 1987-10-31 | 1989-05-11 | Henkel Kgaa | Verwendung von aminethern als netzmittel fuer textilien |
| DE3823843A1 (de) * | 1988-07-14 | 1990-01-18 | Henkel Kgaa | Haarfaerbemittel-zubereitung |
| AU8943991A (en) * | 1990-11-08 | 1992-06-11 | Henkel Corporation | Polymeric thickeners for aqueous compositions |
| US6002049A (en) * | 1990-11-08 | 1999-12-14 | Henkel Corporation | Polymeric thickeners for aqueous compositions |
| US5563251A (en) * | 1991-01-07 | 1996-10-08 | Condea Vista Company | Process for making surfactants |
| EP0584708B1 (de) * | 1992-08-22 | 1998-05-13 | Clariant GmbH | Polyfunktionelle Demulgatoren für Rohöle |
| DE4308794C1 (de) * | 1993-03-18 | 1994-04-21 | Henkel Kgaa | Verfahren zur Herstellung von festen Esterquats mit verbesserter Wasserdispergierbarkeit |
| US5389134A (en) * | 1994-07-18 | 1995-02-14 | Xerox Corporation | Ink compositions for ink jet printing |
| US5573707A (en) * | 1994-11-10 | 1996-11-12 | Henkel Corporation | Process for reducing foam in an aqueous alkyl polyglycoside composition |
| EP0780447B1 (de) * | 1995-12-22 | 2002-10-30 | Ciba SC Holding AG | Wässrige Farbstofflösungen |
| US5936107A (en) * | 1996-12-09 | 1999-08-10 | Henkel Kommanditgesellschaft Auf Aktien | Process for the production of fatty acid polyethylene glycol esters |
| US6110977A (en) * | 1997-01-14 | 2000-08-29 | Henkel Corporation | Alkyl polyglycoside compositions having reduced viscosity and inhibited crystallization |
| US5895605A (en) * | 1997-01-14 | 1999-04-20 | Henkel Corporation | Defoaming compositions |
| US5877245A (en) * | 1997-06-10 | 1999-03-02 | Henkel Corporation | Cross-linked reaction products of alkoxylated alcohols and alkylene glycols |
| DE19754314A1 (de) * | 1997-12-08 | 1999-06-10 | Henkel Kgaa | Hilfsmittel für die Herstellung von Cellulosefasern |
| US5962749A (en) * | 1997-12-24 | 1999-10-05 | Bayer Corporation | Process for the removal of alkalinity in the manufacture of polyether polyols and the reuse of this alkalinity in the manufacture of polyether polyols |
| US6532973B1 (en) * | 1999-06-10 | 2003-03-18 | Cognis Corporation | Gloss retention compositions |
| US6437185B1 (en) * | 1999-06-16 | 2002-08-20 | Finetex, Inc. | Quaternary ammonium compounds and process for preparing and using same |
| US6566317B2 (en) * | 2000-04-25 | 2003-05-20 | Cognis Corporation | Process for inhibiting gel formation of hydrated detergent tablets containing nonionic surfactant ethoxylates |
| US20020103102A1 (en) * | 2000-12-18 | 2002-08-01 | Gross Stephen F. | Branched reaction products of amines and multifunctional compounds |
| US6617412B2 (en) * | 2001-10-12 | 2003-09-09 | Bayer Corporation | Fertilizer encapsulation using sulfur containing polyols |
-
2002
- 2002-10-04 US US10/265,004 patent/US7247606B2/en not_active Expired - Fee Related
- 2002-10-31 JP JP2003542316A patent/JP2005508392A/ja active Pending
- 2002-10-31 AU AU2002363470A patent/AU2002363470A1/en not_active Abandoned
- 2002-10-31 WO PCT/US2002/034844 patent/WO2003040277A2/en not_active Ceased
- 2002-10-31 EP EP02791198A patent/EP1441827B1/en not_active Expired - Lifetime
- 2002-10-31 ES ES02791198T patent/ES2404892T3/es not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| WO2003040277A2 (en) | 2003-05-15 |
| WO2003040277A3 (en) | 2003-10-30 |
| EP1441827A2 (en) | 2004-08-04 |
| EP1441827A4 (en) | 2007-06-20 |
| US7247606B2 (en) | 2007-07-24 |
| AU2002363470A1 (en) | 2003-05-19 |
| ES2404892T3 (es) | 2013-05-29 |
| EP1441827B1 (en) | 2013-03-27 |
| US20030162842A1 (en) | 2003-08-28 |
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