JP2015519413A - 第四級アンモニウム基を含む低粘度ポリオルガノシロキサン、その製造方法および用途（ｉｉ） - Google Patents
第四級アンモニウム基を含む低粘度ポリオルガノシロキサン、その製造方法および用途（ｉｉ） Download PDFInfo
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- JP2015519413A JP2015519413A JP2015503453A JP2015503453A JP2015519413A JP 2015519413 A JP2015519413 A JP 2015519413A JP 2015503453 A JP2015503453 A JP 2015503453A JP 2015503453 A JP2015503453 A JP 2015503453A JP 2015519413 A JP2015519413 A JP 2015519413A
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- polyorganosiloxane
- polyorganosiloxane compound
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- 125000001453 quaternary ammonium group Chemical group 0.000 title claims abstract description 56
- 238000004519 manufacturing process Methods 0.000 title description 4
- 150000001875 compounds Chemical class 0.000 claims abstract description 183
- 239000000203 mixture Substances 0.000 claims abstract description 110
- 125000004185 ester group Chemical group 0.000 claims abstract description 77
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 56
- 229920000570 polyether Polymers 0.000 claims abstract description 56
- 238000002360 preparation method Methods 0.000 claims abstract description 29
- 238000000034 method Methods 0.000 claims abstract description 17
- 239000000839 emulsion Substances 0.000 claims abstract description 9
- 239000000758 substrate Substances 0.000 claims abstract description 3
- -1 polysiloxane Polymers 0.000 claims description 109
- 229920001296 polysiloxane Polymers 0.000 claims description 60
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims description 59
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 48
- 125000004432 carbon atom Chemical group C* 0.000 claims description 43
- POULHZVOKOAJMA-UHFFFAOYSA-N dodecanoic acid Chemical compound CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 42
- 229920000642 polymer Polymers 0.000 claims description 36
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 125000004122 cyclic group Chemical group 0.000 claims description 22
- 125000000524 functional group Chemical group 0.000 claims description 22
- 150000001735 carboxylic acids Chemical class 0.000 claims description 18
- 238000006243 chemical reaction Methods 0.000 claims description 18
- 229920006395 saturated elastomer Polymers 0.000 claims description 18
- 125000003118 aryl group Chemical group 0.000 claims description 17
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 17
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- 125000005842 heteroatom Chemical group 0.000 claims description 11
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 11
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium group Chemical group [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 10
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 10
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 claims description 9
- 229910052799 carbon Inorganic materials 0.000 claims description 9
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- 229940126062 Compound A Drugs 0.000 claims description 8
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims description 8
- 125000000129 anionic group Chemical group 0.000 claims description 8
- 125000000962 organic group Chemical group 0.000 claims description 8
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- 150000001412 amines Chemical class 0.000 claims description 6
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- 125000002091 cationic group Chemical group 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 6
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 claims description 6
- 125000001424 substituent group Chemical group 0.000 claims description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 5
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- 239000001257 hydrogen Substances 0.000 claims description 5
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 claims description 5
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- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 claims description 3
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 claims description 3
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 claims description 3
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- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 claims description 3
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- 239000000835 fiber Substances 0.000 claims description 3
- 238000011010 flushing procedure Methods 0.000 claims description 3
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 claims description 3
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 claims description 3
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 claims description 3
- FRPZMMHWLSIFAZ-UHFFFAOYSA-N 10-undecenoic acid Chemical compound OC(=O)CCCCCCCCC=C FRPZMMHWLSIFAZ-UHFFFAOYSA-N 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
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- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 claims description 2
- 229960003656 ricinoleic acid Drugs 0.000 claims description 2
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 claims description 2
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- KWIUHFFTVRNATP-UHFFFAOYSA-O N,N,N-trimethylglycinium Chemical compound C[N+](C)(C)CC(O)=O KWIUHFFTVRNATP-UHFFFAOYSA-O 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 1
- 125000004427 diamine group Chemical group 0.000 claims 1
- 150000005690 diesters Chemical class 0.000 claims 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 41
- 238000009472 formulation Methods 0.000 description 40
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 36
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 35
- 239000002904 solvent Substances 0.000 description 31
- 235000014113 dietary fatty acids Nutrition 0.000 description 28
- 239000000194 fatty acid Substances 0.000 description 28
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- 239000004615 ingredient Substances 0.000 description 28
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 25
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 description 25
- 238000010992 reflux Methods 0.000 description 23
- 239000002253 acid Substances 0.000 description 22
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 22
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- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 18
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- 238000005259 measurement Methods 0.000 description 13
- TXXWBTOATXBWDR-UHFFFAOYSA-N n,n,n',n'-tetramethylhexane-1,6-diamine Chemical compound CN(C)CCCCCCN(C)C TXXWBTOATXBWDR-UHFFFAOYSA-N 0.000 description 13
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 12
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- 235000013343 vitamin Nutrition 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
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Classifications
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- 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
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/22—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen
- C08G77/26—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen and oxygen nitrogen-containing groups
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- 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
- A61K8/896—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
- A61K8/898—Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
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- 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
- A61Q5/02—Preparations for cleaning the hair
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- 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
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
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- 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
- 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
- C08G77/04—Polysiloxanes
- C08G77/06—Preparatory processes
-
- 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
- C09D183/00—Coating compositions based on 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; Coating compositions based on derivatives of such polymers
- C09D183/04—Polysiloxanes
- C09D183/08—Polysiloxanes containing silicon bound to organic groups containing atoms other than carbon, hydrogen, and oxygen
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/0005—Other compounding ingredients characterised by their effect
- C11D3/001—Softening compositions
-
- 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
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/37—Polymers
- C11D3/3703—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- C11D3/373—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicones
- C11D3/3742—Nitrogen containing silicones
-
- 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
- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/46—Compounds containing quaternary nitrogen atoms
-
- 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
-
- 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
- D06M15/6433—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing carboxylic groups
-
- 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
- D06M15/65—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing epoxy groups
- D06M15/651—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds containing silicon in the main chain containing epoxy groups comprising carboxylic groups
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/14—Polysiloxanes containing silicon bound to oxygen-containing groups
-
- 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
- C08G77/04—Polysiloxanes
- C08G77/38—Polysiloxanes modified by chemical after-treatment
- C08G77/382—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon
- C08G77/388—Polysiloxanes modified by chemical after-treatment containing atoms other than carbon, hydrogen, oxygen or silicon containing nitrogen
-
- 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
- C11D2111/00—Cleaning compositions characterised by the objects to be cleaned; Cleaning compositions characterised by non-standard cleaning or washing processes
- C11D2111/10—Objects to be cleaned
- C11D2111/12—Soft surfaces, e.g. textile
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
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- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Materials Engineering (AREA)
- Silicon Polymers (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
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| US201261617180P | 2012-03-29 | 2012-03-29 | |
| US61/617,180 | 2012-03-29 | ||
| PCT/US2013/033816 WO2013148635A1 (en) | 2012-03-29 | 2013-03-26 | Low viscosity polyorganosiloxanes comprising quaternary ammonium groups, methods for the production and the use thereof (ii) |
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| JP2015519413A true JP2015519413A (ja) | 2015-07-09 |
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| JP2015503449A Pending JP2015514879A (ja) | 2012-03-29 | 2013-03-26 | 第四級アンモニウム基を含む低粘度であるポリオルガノシロキサン、その製造方法ならびにそれらの使用 |
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Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015512410A (ja) * | 2012-03-29 | 2015-04-27 | ザ プロクター アンド ギャンブルカンパニー | 低粘度シリコーンポリマーを含むヘアコンディショニング組成物 |
| JP2019522713A (ja) * | 2016-07-13 | 2019-08-15 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハーＭｏｍｅｎｔｉｖｅ Ｐｅｒｆｏｒｍａｎｃｅ Ｍａｔｅｒｉａｌｓ ＧｍｂＨ | 四級アンモニウム基を含む低粘度ポリオルガノシロキサン、その製造方法およびその使用 |
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| JP2015519413A (ja) | 2012-03-29 | 2015-07-09 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハー | 第四級アンモニウム基を含む低粘度ポリオルガノシロキサン、その製造方法および用途（ｉｉ） |
| WO2013148935A1 (en) | 2012-03-29 | 2013-10-03 | Momentive Performance Materials Inc. | Low viscosity polyorganosiloxanes comprising quaternary ammonium groups, methods for the production and the use thereof |
| US20150010487A1 (en) * | 2013-07-03 | 2015-01-08 | The Procter & Gamble Company | Shampoo composition comprising low viscosity silicone polymers |
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| US20240301228A1 (en) * | 2021-07-19 | 2024-09-12 | Hewlett-Packard Development Company, L.P. | Multi-fluid kit for textile printing |
| CA3235522A1 (en) | 2021-12-09 | 2023-06-15 | The Procter & Gamble Company | Sulfate free personal cleansing composition comprising effective preservation |
| CN119998361A (zh) * | 2022-06-02 | 2025-05-13 | 迈图高新材料公司 | 聚硅氧烷聚合物组合物及其制备方法 |
Family Cites Families (25)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3705121A1 (de) | 1987-02-18 | 1988-09-01 | Goldschmidt Ag Th | Polyquaternaere polysiloxan-polymere, deren herstellung und verwendung in kosmetischen zubereitungen |
| DE3719086C1 (de) | 1987-06-06 | 1988-10-27 | Goldschmidt Ag Th | Diquartaere Polysiloxane,deren Herstellung und Verwendung in kosmetischen Zubereitungen |
| DE3802622A1 (de) | 1988-01-29 | 1989-08-10 | Goldschmidt Ag Th | Mittel zum ausruesten von textilfasern oder aus textilfasern bestehenden produkten |
| US5166297A (en) | 1991-03-25 | 1992-11-24 | Siltech Inc. | Silicone ester quaternary compounds |
| US5098979A (en) | 1991-03-25 | 1992-03-24 | Siltech Inc. | Novel silicone quaternary compounds |
| US5153294A (en) | 1991-03-25 | 1992-10-06 | Siltech Inc. | Silicone ester quaternary compounds |
| FR2777010B1 (fr) | 1998-04-01 | 2000-06-16 | Oreal | Polymeres silicies de polyammonium quaternaire heterocyclique et leur utilisation dans les compositions cosmetiques |
| EP1000959B1 (de) | 1998-11-14 | 2003-04-16 | Goldschmidt AG | Polyetherquatfunktionelle Polysiloxane |
| US7041767B2 (en) | 2000-07-27 | 2006-05-09 | Ge Bayer Silicones Gmbh & Co. Kg | Polysiloxane polymers, method for their production and the use thereof |
| AU2001291687A1 (en) | 2000-07-27 | 2002-02-13 | Ge Bayer Silicones Gmbh And Co. Kg | Polyammonium-polysiloxane compounds, methods for the production and use thereof |
| US6903061B2 (en) | 2000-08-28 | 2005-06-07 | The Procter & Gamble Company | Fabric care and perfume compositions and systems comprising cationic silicones and methods employing same |
| DE10139963A1 (de) | 2001-08-14 | 2003-03-06 | Wacker Chemie Gmbh | Quaternäre Ammoniumgruppen aufweisende Organopolysiloxane und Verfahren zu deren Herstellung |
| JP4801322B2 (ja) | 2002-03-20 | 2011-10-26 | モーメンテイブ・パーフオーマンス・マテリアルズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング | 分枝ポリオルガノシロキサン重合体 |
| JP2006505716A (ja) * | 2002-11-04 | 2006-02-16 | ジーイー・バイエル・シリコーンズ・ゲゼルシヤフト・ミツト・ベシユレンクテル・ハフツング・ウント・コンパニー・コマンジツトゲゼルシヤフト | 基質表面の処理のために使用される調合物 |
| DE10316662A1 (de) | 2003-04-11 | 2004-11-11 | Ge Bayer Silicones Gmbh & Co. Kg | Reaktive Amino- und/oder Ammonium-Polysiloxanverbindungen |
| 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 |
| US20070041929A1 (en) | 2005-06-16 | 2007-02-22 | Torgerson Peter M | Hair conditioning composition comprising silicone polymers containing quaternary groups |
| DE102005036602A1 (de) * | 2005-08-01 | 2007-02-08 | Ge Bayer Silicones Gmbh & Co. Kg | Polyammonium-Polysiloxancopolymere |
| US20070286837A1 (en) | 2006-05-17 | 2007-12-13 | Torgerson Peter M | Hair care composition comprising an aminosilicone and a high viscosity silicone copolymer emulsion |
| DE102006035512A1 (de) * | 2006-07-31 | 2008-02-07 | Evonik Goldschmidt Gmbh | Neuartige Polysiloxane mit quaternären Ammoniumgruppen, Verfahren zu deren Herstellung und deren Verwendung in reinigenden und pflegenden Formulierungen |
| US8728450B2 (en) | 2007-05-23 | 2014-05-20 | The Procter & Gamble Company | Hair conditioning composition comprising quaternized silicone polymer, grafted silicone copolyol, and dialkyl cationic surfactant |
| DE102008014761A1 (de) | 2008-03-18 | 2009-12-10 | Momentive Performance Materials Gmbh | Verwendung von Polyamino- und/oder Polyammonium-Polysiloxan-Copolymer-Verbindungen |
| KR101627304B1 (ko) | 2009-11-24 | 2016-06-03 | 모멘티브 퍼포먼스 머티리얼즈 게엠베하 | 친수성/친유성 개질된 유화제로서의 폴리실록산 |
| JP2015519413A (ja) | 2012-03-29 | 2015-07-09 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハー | 第四級アンモニウム基を含む低粘度ポリオルガノシロキサン、その製造方法および用途（ｉｉ） |
| WO2013148935A1 (en) | 2012-03-29 | 2013-10-03 | Momentive Performance Materials Inc. | Low viscosity polyorganosiloxanes comprising quaternary ammonium groups, methods for the production and the use thereof |
-
2013
- 2013-03-26 JP JP2015503453A patent/JP2015519413A/ja active Pending
- 2013-03-26 US US14/389,195 patent/US9512275B2/en active Active
- 2013-03-26 IN IN1906MUN2014 patent/IN2014MN01906A/en unknown
- 2013-03-26 EP EP13716586.6A patent/EP2831177B1/en active Active
- 2013-03-26 WO PCT/US2013/033806 patent/WO2013148629A1/en not_active Ceased
- 2013-03-26 WO PCT/US2013/033816 patent/WO2013148635A1/en not_active Ceased
- 2013-03-26 BR BR112014024182-1A patent/BR112014024182B1/pt active IP Right Grant
- 2013-03-26 US US14/387,599 patent/US9428616B2/en active Active
- 2013-03-26 CN CN201380025746.1A patent/CN104302705B/zh active Active
- 2013-03-26 EP EP18162000.6A patent/EP3357973B1/en active Active
- 2013-03-26 EP EP13717095.7A patent/EP2831178B1/en active Active
- 2013-03-26 JP JP2015503449A patent/JP2015514879A/ja active Pending
- 2013-03-26 IN IN1877MUN2014 patent/IN2014MN01877A/en unknown
- 2013-03-26 CN CN201380026194.6A patent/CN104334646B/zh active Active
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2015512410A (ja) * | 2012-03-29 | 2015-04-27 | ザ プロクター アンド ギャンブルカンパニー | 低粘度シリコーンポリマーを含むヘアコンディショニング組成物 |
| JP2019522713A (ja) * | 2016-07-13 | 2019-08-15 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハーＭｏｍｅｎｔｉｖｅ Ｐｅｒｆｏｒｍａｎｃｅ Ｍａｔｅｒｉａｌｓ ＧｍｂＨ | 四級アンモニウム基を含む低粘度ポリオルガノシロキサン、その製造方法およびその使用 |
| JP7328887B2 (ja) | 2016-07-13 | 2023-08-17 | モメンティブ パフォーマンス マテリアルズ ゲーエムベーハー | 四級アンモニウム基を含む低粘度ポリオルガノシロキサン、その製造方法およびその使用 |
Also Published As
| Publication number | Publication date |
|---|---|
| BR112014024182A2 (pt) | 2017-06-20 |
| WO2013148635A1 (en) | 2013-10-03 |
| IN2014MN01906A (enExample) | 2015-07-10 |
| BR112014024182B1 (pt) | 2021-06-29 |
| US20150299400A1 (en) | 2015-10-22 |
| WO2013148629A1 (en) | 2013-10-03 |
| EP2831177B1 (en) | 2018-05-09 |
| CN104334646B (zh) | 2017-02-22 |
| EP2831178A1 (en) | 2015-02-04 |
| US9428616B2 (en) | 2016-08-30 |
| CN104302705B (zh) | 2017-04-12 |
| EP3357973A1 (en) | 2018-08-08 |
| CN104334646A (zh) | 2015-02-04 |
| EP2831178B1 (en) | 2020-07-22 |
| US20150056155A1 (en) | 2015-02-26 |
| CN104302705A (zh) | 2015-01-21 |
| JP2015514879A (ja) | 2015-05-21 |
| EP3357973B1 (en) | 2019-07-31 |
| IN2014MN01877A (enExample) | 2015-07-03 |
| US9512275B2 (en) | 2016-12-06 |
| EP2831177A1 (en) | 2015-02-04 |
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