BR112014011787B1 - copolímero tribloco linear de óxido de polialquileno silicone, métodos de preparação, composição de silicone ou composição de rede de silicone, composição para cuidado pessoal, composição amaciadora, e condicionador de cabelo - Google Patents
copolímero tribloco linear de óxido de polialquileno silicone, métodos de preparação, composição de silicone ou composição de rede de silicone, composição para cuidado pessoal, composição amaciadora, e condicionador de cabelo Download PDFInfo
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- BR112014011787B1 BR112014011787B1 BR112014011787-0A BR112014011787A BR112014011787B1 BR 112014011787 B1 BR112014011787 B1 BR 112014011787B1 BR 112014011787 A BR112014011787 A BR 112014011787A BR 112014011787 B1 BR112014011787 B1 BR 112014011787B1
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- -1 preparation methods Polymers 0.000 title claims abstract description 35
- 210000004209 hair Anatomy 0.000 title claims abstract description 26
- 229920001296 polysiloxane Polymers 0.000 title claims abstract description 22
- 239000000203 mixture Substances 0.000 title claims abstract description 21
- 229920000233 poly(alkylene oxides) Polymers 0.000 title claims abstract description 20
- 238000002360 preparation method Methods 0.000 title abstract description 8
- 229920001400 block copolymer Polymers 0.000 title description 6
- 229920000428 triblock copolymer Polymers 0.000 claims abstract description 30
- 229920001577 copolymer Polymers 0.000 claims abstract description 28
- 150000003335 secondary amines Chemical class 0.000 claims abstract description 23
- 150000003512 tertiary amines Chemical class 0.000 claims abstract description 14
- 238000000034 method Methods 0.000 claims abstract description 12
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 7
- 125000000962 organic group Chemical group 0.000 claims abstract description 5
- 150000002118 epoxides Chemical class 0.000 claims abstract 15
- 125000004432 carbon atom Chemical group C* 0.000 claims description 19
- 239000004593 Epoxy Substances 0.000 claims description 17
- 125000002947 alkylene group Chemical group 0.000 claims description 16
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 14
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- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 claims description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 9
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 3
- 239000002453 shampoo Substances 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 2
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- 239000004743 Polypropylene Substances 0.000 claims description 2
- 125000003342 alkenyl group Chemical group 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 229910052799 carbon Inorganic materials 0.000 claims description 2
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- 210000002268 wool Anatomy 0.000 claims description 2
- 125000001570 methylene group Chemical group [H]C([H])([*:1])[*:2] 0.000 claims 4
- 239000000047 product Substances 0.000 claims 2
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims 1
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- STMDPCBYJCIZOD-UHFFFAOYSA-N 2-(2,4-dinitroanilino)-4-methylpentanoic acid Chemical compound CC(C)CC(C(O)=O)NC1=CC=C([N+]([O-])=O)C=C1[N+]([O-])=O STMDPCBYJCIZOD-UHFFFAOYSA-N 0.000 description 3
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- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- 239000003795 chemical substances by application Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical compound OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 3
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- 239000007788 liquid Substances 0.000 description 2
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- 239000004094 surface-active agent Substances 0.000 description 2
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- QDRMUFJWOJOOKR-UHFFFAOYSA-N 1-(1-hydroxypropan-2-yloxy)butan-2-ol Chemical compound CCC(O)COC(C)CO QDRMUFJWOJOOKR-UHFFFAOYSA-N 0.000 description 1
- IXPNQXFRVYWDDI-UHFFFAOYSA-N 1-methyl-2,4-dioxo-1,3-diazinane-5-carboximidamide Chemical compound CN1CC(C(N)=N)C(=O)NC1=O IXPNQXFRVYWDDI-UHFFFAOYSA-N 0.000 description 1
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- 229920000856 Amylose Polymers 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
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- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 1
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- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000007810 chemical reaction solvent Substances 0.000 description 1
- 230000003749 cleanliness Effects 0.000 description 1
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- 230000003766 combability Effects 0.000 description 1
- 125000002704 decyl group Chemical group [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])* 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- SMVRDGHCVNAOIN-UHFFFAOYSA-L disodium;1-dodecoxydodecane;sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O.CCCCCCCCCCCCOCCCCCCCCCCCC SMVRDGHCVNAOIN-UHFFFAOYSA-L 0.000 description 1
- 238000004821 distillation Methods 0.000 description 1
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 1
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
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- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 150000002430 hydrocarbons Chemical group 0.000 description 1
- 229920001477 hydrophilic polymer Polymers 0.000 description 1
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- 230000003752 improving hair Effects 0.000 description 1
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- 125000002960 margaryl 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])[H] 0.000 description 1
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- 125000001421 myristyl 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])[H] 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 125000001196 nonadecyl 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])C([H])([H])[H] 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- 125000005702 oxyalkylene group Chemical group 0.000 description 1
- 125000000913 palmityl 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])[H] 0.000 description 1
- 125000002958 pentadecyl 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])[H] 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
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- 239000003755 preservative agent Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 238000007086 side reaction Methods 0.000 description 1
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- FVEFRICMTUKAML-UHFFFAOYSA-M sodium tetradecyl sulfate Chemical compound [Na+].CCCCC(CC)CCC(CC(C)C)OS([O-])(=O)=O FVEFRICMTUKAML-UHFFFAOYSA-M 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000005507 spraying Methods 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
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- 230000003655 tactile properties Effects 0.000 description 1
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- 125000003944 tolyl group Chemical group 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
- 125000002948 undecyl 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])[H] 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0834—Compounds having one or more O-Si linkage
- C07F7/0838—Compounds with one or more Si-O-Si sequences
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
- A61K8/894—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/12—Preparations containing hair conditioners
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/10—Compounds having one or more C—Si linkages containing nitrogen having a Si-N linkage
-
- 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
- C08G77/00—Macromolecular compounds obtained by reactions forming a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon in the main chain of the macromolecule
- C08G77/42—Block-or graft-polymers containing polysiloxane sequences
- C08G77/46—Block-or graft-polymers containing polysiloxane sequences containing polyether sequences
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L83/00—Compositions of macromolecular compounds obtained by reactions forming in the main chain of the macromolecule a linkage containing silicon with or without sulfur, nitrogen, oxygen or carbon only; Compositions of derivatives of such polymers
- C08L83/10—Block- or graft-copolymers containing polysiloxane sequences
- C08L83/12—Block- or graft-copolymers containing polysiloxane sequences containing polyether sequences
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/643—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain
- D06M15/647—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing polyether sequences
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Engineering & Computer Science (AREA)
- Dermatology (AREA)
- Textile Engineering (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Silicon Polymers (AREA)
- Cosmetics (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US13/297.931 | 2011-11-16 | ||
| US13/297,931 US8742154B2 (en) | 2011-11-16 | 2011-11-16 | Block ABA silicone polyalkyleneoxicie copolymers, methods of preparation, and applications for employing the same |
| PCT/US2012/065496 WO2013074912A1 (en) | 2011-11-16 | 2012-11-16 | Block aba silicone polyalkylene oxide copolymers, methods of preparation, and applications for employing the same |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| BR112014011787A2 BR112014011787A2 (pt) | 2017-05-09 |
| BR112014011787B1 true BR112014011787B1 (pt) | 2020-10-13 |
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| BR112014011787-0A BR112014011787B1 (pt) | 2011-11-16 | 2012-11-16 | copolímero tribloco linear de óxido de polialquileno silicone, métodos de preparação, composição de silicone ou composição de rede de silicone, composição para cuidado pessoal, composição amaciadora, e condicionador de cabelo |
Country Status (10)
| Country | Link |
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| US (1) | US8742154B2 (enExample) |
| EP (1) | EP2780396B1 (enExample) |
| JP (1) | JP6624783B2 (enExample) |
| KR (1) | KR101987825B1 (enExample) |
| CN (1) | CN104053703B (enExample) |
| BR (1) | BR112014011787B1 (enExample) |
| CA (1) | CA2854915A1 (enExample) |
| IN (1) | IN2014MN00905A (enExample) |
| MX (1) | MX2014005783A (enExample) |
| WO (1) | WO2013074912A1 (enExample) |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US11111339B2 (en) * | 2015-12-04 | 2021-09-07 | Momentive Performance Materials Inc. | Polyacrylate salt, methods of preparation and applications for employing the same |
| WO2017182061A1 (en) | 2016-04-19 | 2017-10-26 | Wacker Chemie Ag | Amino-organopolysiloxane and preparation method thereof |
| BR112018072818B8 (pt) * | 2016-05-10 | 2022-11-16 | Dow Silicones Corp | Copolímero de bloco de silicone, processo para preparação de um copolímero, emulsão, método para tratamento de um substrato, composição para cuidados pessoais, xampu, condicionador para cabelos, e, composição anidra de tratamento capilar sem enxágue |
| CN107938360B (zh) * | 2016-12-19 | 2020-02-07 | 广州大学 | 一种高性能织物整理乳液 |
| ES2954421T3 (es) * | 2017-03-21 | 2023-11-22 | Solenis Tech Lp | Una composición y un método de producción de un papel crepado y el papel crepado del mismo |
| CN110637047B (zh) | 2017-05-31 | 2021-11-12 | 东丽株式会社 | 嵌段共聚物及其制造方法、环氧树脂组合物及其固化物及半导体密封材料 |
| CN108276581A (zh) * | 2017-12-22 | 2018-07-13 | 浙江雀屏纺织化工股份有限公司 | 一种低溶剂嵌段硅油的合成方法及包含该低溶剂嵌段硅油的手感整理剂 |
| WO2020232675A1 (en) * | 2019-05-22 | 2020-11-26 | Huntsman Petrochemical Llc | Amine compound with good hydrophilicity |
| WO2020261192A1 (en) | 2019-06-27 | 2020-12-30 | Wacker Metroark Chemicals Pvt. Ltd. | Hydrophillic silicone made of olefinic unsaturated polyoxyalkylene glycidyl ether, its composition and preparation method thereof |
| CA3163027A1 (en) * | 2019-12-25 | 2021-07-01 | Dow Toray Co., Ltd. | Polyether-polysiloxane block copolymer composition, foam stabilizer and method for producing polyurethane foam |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US1213779A (en) | 1914-10-22 | 1917-01-23 | Gould Coupler Co | Slack-adjuster. |
| DE1768785C3 (de) | 1968-06-29 | 1975-01-23 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von OrganosiHciumverbindungen |
| US3761444A (en) | 1969-08-18 | 1973-09-25 | Union Carbide Corp | Equilibration of epoxy substituted siloxanes in presence of water andsilanol |
| AU1823676A (en) | 1975-10-13 | 1978-04-06 | Commw Scient Ind Res Org | Treatment of wool with polyorganosiloxanes |
| WO1997032917A1 (en) | 1996-03-04 | 1997-09-12 | Osi Specialities, Inc. | Silicone aminopolyalkyleneoxide block copolymers |
| US6475568B1 (en) | 2001-05-15 | 2002-11-05 | Crompton Corporation | Block, non-(AB)n silicone polyalkyleneoxide copolymers with tertiary amino links |
| DE60230440D1 (de) * | 2001-11-28 | 2009-01-29 | Shinetsu Chemical Co | Haarpflegeprodukte |
| DE102005014311A1 (de) * | 2005-03-30 | 2006-10-12 | Ge Bayer Silicones Gmbh & Co. Kg | Polyamino- und/oder Polyammonium-Polysiloxan-Colpolymer-Verbindungen mit kammartig angeordneten Polyalkylenonideinheiten |
| EP2139941A1 (en) | 2007-04-11 | 2010-01-06 | Dow Corning Corporation | Silcone polyether block copolymers having organofunctional endblocking groups |
| US7851548B2 (en) | 2008-05-01 | 2010-12-14 | Momentive Performance Materials Inc. | Low viscosity, high molecular weight linear random-block silicone polyalkyleneoxide copolymers |
| DE102010001350A1 (de) * | 2010-01-29 | 2011-08-04 | Evonik Goldschmidt GmbH, 45127 | Neuartige lineare Polydimethylsiloxan-Polyether-Copolymere mit Amino- und/oder quaternären Ammoniumgruppen und deren Verwendung |
| HUE044765T2 (hu) * | 2010-10-06 | 2019-11-28 | Novartis Ag | Polimerizálható hosszabbított láncú polisziloxánok hidrofil oldalcsoportokkal |
-
2011
- 2011-11-16 US US13/297,931 patent/US8742154B2/en active Active
-
2012
- 2012-11-16 KR KR1020147013139A patent/KR101987825B1/ko active Active
- 2012-11-16 MX MX2014005783A patent/MX2014005783A/es unknown
- 2012-11-16 CN CN201280066972.XA patent/CN104053703B/zh active Active
- 2012-11-16 CA CA2854915A patent/CA2854915A1/en not_active Abandoned
- 2012-11-16 IN IN905MUN2014 patent/IN2014MN00905A/en unknown
- 2012-11-16 WO PCT/US2012/065496 patent/WO2013074912A1/en not_active Ceased
- 2012-11-16 BR BR112014011787-0A patent/BR112014011787B1/pt active IP Right Grant
- 2012-11-16 JP JP2014542490A patent/JP6624783B2/ja active Active
- 2012-11-16 EP EP12791410.9A patent/EP2780396B1/en not_active Not-in-force
Also Published As
| Publication number | Publication date |
|---|---|
| JP2015504468A (ja) | 2015-02-12 |
| US20130123529A1 (en) | 2013-05-16 |
| US8742154B2 (en) | 2014-06-03 |
| CA2854915A1 (en) | 2013-05-23 |
| BR112014011787A2 (pt) | 2017-05-09 |
| EP2780396A1 (en) | 2014-09-24 |
| MX2014005783A (es) | 2014-05-30 |
| CN104053703B (zh) | 2016-03-02 |
| JP6624783B2 (ja) | 2019-12-25 |
| KR20140095495A (ko) | 2014-08-01 |
| IN2014MN00905A (enExample) | 2015-04-17 |
| CN104053703A (zh) | 2014-09-17 |
| KR101987825B1 (ko) | 2019-06-11 |
| EP2780396B1 (en) | 2015-10-21 |
| WO2013074912A1 (en) | 2013-05-23 |
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| B09A | Decision: intention to grant [chapter 9.1 patent gazette] | ||
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Free format text: PRAZO DE VALIDADE: 20 (VINTE) ANOS CONTADOS A PARTIR DE 16/11/2012, OBSERVADAS AS CONDICOES LEGAIS. |