JP2017501276A5 - - Google Patents
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- Publication number
- JP2017501276A5 JP2017501276A5 JP2016540643A JP2016540643A JP2017501276A5 JP 2017501276 A5 JP2017501276 A5 JP 2017501276A5 JP 2016540643 A JP2016540643 A JP 2016540643A JP 2016540643 A JP2016540643 A JP 2016540643A JP 2017501276 A5 JP2017501276 A5 JP 2017501276A5
- Authority
- JP
- Japan
- Prior art keywords
- organopolysiloxane
- sio
- carbon atoms
- units
- group
- 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.)
- Granted
Links
- 229920001296 polysiloxane Polymers 0.000 claims description 40
- ACIAHEMYLLBZOI-ZZXKWVIFSA-N Unsaturated alcohol Chemical compound CC\C(CO)=C/C ACIAHEMYLLBZOI-ZZXKWVIFSA-N 0.000 claims description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims description 11
- 239000000203 mixture Substances 0.000 claims description 10
- 239000003085 diluting agent Substances 0.000 claims description 8
- 229910052739 hydrogen Inorganic materials 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 8
- 239000011347 resin Substances 0.000 claims description 8
- 229920005989 resin Polymers 0.000 claims description 8
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 7
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- -1 polydimethylsiloxane Polymers 0.000 claims description 5
- 239000004721 Polyphenylene oxide Substances 0.000 claims description 4
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical group [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 4
- 229920000570 polyether Polymers 0.000 claims description 4
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000003054 catalyst Substances 0.000 claims description 2
- 238000006459 hydrosilylation reaction Methods 0.000 claims description 2
- 238000000034 method Methods 0.000 claims 11
- 238000004519 manufacturing process Methods 0.000 claims 5
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims 3
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 claims 3
- 239000002904 solvent Substances 0.000 claims 3
- FFBHFFJDDLITSX-UHFFFAOYSA-N benzyl N-[2-hydroxy-4-(3-oxomorpholin-4-yl)phenyl]carbamate Chemical compound OC1=C(NC(=O)OCC2=CC=CC=C2)C=CC(=C1)N1CCOCC1=O FFBHFFJDDLITSX-UHFFFAOYSA-N 0.000 claims 2
- 239000002537 cosmetic Substances 0.000 claims 2
- 239000008240 homogeneous mixture Substances 0.000 claims 2
- 229910004298 SiO 2 Inorganic materials 0.000 claims 1
- 239000004480 active ingredient Substances 0.000 claims 1
- 125000002723 alicyclic group Chemical group 0.000 claims 1
- 238000003763 carbonization Methods 0.000 claims 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000004205 dimethyl polysiloxane Substances 0.000 claims 1
- 150000002148 esters Chemical class 0.000 claims 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 150000002430 hydrocarbons Chemical group 0.000 description 9
- 229930195733 hydrocarbon Natural products 0.000 description 4
- SGVYKUFIHHTIFL-UHFFFAOYSA-N 2-methylnonane Chemical compound CCCCCCCC(C)C SGVYKUFIHHTIFL-UHFFFAOYSA-N 0.000 description 3
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 3
- QEGNUYASOUJEHD-UHFFFAOYSA-N 1,1-dimethylcyclohexane Chemical compound CC1(C)CCCCC1 QEGNUYASOUJEHD-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- 150000004808 allyl alcohols Polymers 0.000 description 2
- DMEGYFMYUHOHGS-UHFFFAOYSA-N cycloheptane Chemical compound C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 0.000 description 2
- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 2
- IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 2
- UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
- TVMXDCGIABBOFY-UHFFFAOYSA-N octane Chemical compound CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 2
- GTJOHISYCKPIMT-UHFFFAOYSA-N 2-methylundecane Chemical compound CCCCCCCCCC(C)C GTJOHISYCKPIMT-UHFFFAOYSA-N 0.000 description 1
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 1
- NHTMVDHEPJAVLT-UHFFFAOYSA-N Isooctane Chemical compound CC(C)CC(C)(C)C NHTMVDHEPJAVLT-UHFFFAOYSA-N 0.000 description 1
- 239000002202 Polyethylene glycol Substances 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- WJTCGQSWYFHTAC-UHFFFAOYSA-N cyclooctane Chemical compound C1CCCCCCC1 WJTCGQSWYFHTAC-UHFFFAOYSA-N 0.000 description 1
- 239000004914 cyclooctane Substances 0.000 description 1
- JVSWJIKNEAIKJW-UHFFFAOYSA-N dimethyl-hexane Natural products CCCCCC(C)C JVSWJIKNEAIKJW-UHFFFAOYSA-N 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N dodecane Chemical compound CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- VKPSKYDESGTTFR-UHFFFAOYSA-N isododecane Natural products CC(C)(C)CC(C)CC(C)(C)C VKPSKYDESGTTFR-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
- 229940094933 n-dodecane Drugs 0.000 description 1
- CLMFECCMAVQYQA-UHFFFAOYSA-N nonylcyclohexane Chemical compound CCCCCCCCCC1CCCCC1 CLMFECCMAVQYQA-UHFFFAOYSA-N 0.000 description 1
- 125000006353 oxyethylene group Chemical group 0.000 description 1
- 229920001223 polyethylene glycol Polymers 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 229930195735 unsaturated hydrocarbon Natural products 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102013226249.3 | 2013-12-17 | ||
| DE102013226249.3A DE102013226249A1 (de) | 2013-12-17 | 2013-12-17 | Polyetherreste aufweisende Organopolysiloxangele |
| PCT/EP2014/077804 WO2015091381A1 (de) | 2013-12-17 | 2014-12-15 | Polyetherreste aufweisende organopolysiloxangele |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2017501276A JP2017501276A (ja) | 2017-01-12 |
| JP2017501276A5 true JP2017501276A5 (https=) | 2017-11-02 |
| JP6313451B2 JP6313451B2 (ja) | 2018-04-18 |
Family
ID=52273102
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2016540643A Active JP6313451B2 (ja) | 2013-12-17 | 2014-12-15 | ポリエーテル基を有するポリオルガノシロキサンゲル |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US9770403B2 (https=) |
| EP (1) | EP3083766B1 (https=) |
| JP (1) | JP6313451B2 (https=) |
| KR (1) | KR101883580B1 (https=) |
| CN (1) | CN105980448B (https=) |
| DE (1) | DE102013226249A1 (https=) |
| WO (1) | WO2015091381A1 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP6705587B2 (ja) * | 2015-09-17 | 2020-06-03 | 尾池 哲郎 | 流動性を有した脂肪酸ナトリウム石鹸の製造方法 |
| US11654098B2 (en) * | 2017-06-12 | 2023-05-23 | Wacker Chemie Ag | Process for preparing organopolysiloane gels |
| CN110832033A (zh) * | 2017-07-21 | 2020-02-21 | 美国陶氏有机硅公司 | 可固化有机聚硅氧烷组合物及其固化产物 |
| US20200222302A1 (en) * | 2017-08-31 | 2020-07-16 | Dow Silicones Corporation | Film forming compositions having a tack-free surface |
| CN107722282A (zh) * | 2017-09-28 | 2018-02-23 | 广州天赐高新材料股份有限公司 | 一种基于乙烯基mq硅树脂的有机硅弹性体及其制备方法 |
| WO2020036873A1 (en) * | 2018-08-13 | 2020-02-20 | Gpcp Ip Holdings Llc | Cleaning formulations with liquid repellency |
| US20220168217A1 (en) * | 2019-02-22 | 2022-06-02 | Elkem Silicones USA Corp. | Drug delivery silicone composition to improve active ingredient elution |
| CN110028793B (zh) * | 2019-04-19 | 2020-08-18 | 浙江新安化工集团股份有限公司 | 一种有机硅弹性体、其制备方法及包含其的有机硅弹性体凝胶 |
| WO2021134118A1 (en) * | 2019-12-30 | 2021-07-08 | L'oreal | Cosmetic composition comprising a fatty amine, a fatty alcohol, a vegetable fat, a cationic surfactant and a silicone cross-polymer for use in hair care |
| US20230331919A1 (en) * | 2020-09-24 | 2023-10-19 | Wacker Chemie Ag | Method for producing hydrophilic organopolysiloxane gels |
Family Cites Families (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2624874B1 (fr) | 1987-12-18 | 1990-06-08 | Dow Corning Sa | Composition gelifiable a base d'organosiloxanes, gel produit a partir de cette composition, et pansement et prothese contenant ce gel |
| KR970706356A (ko) * | 1994-09-30 | 1997-11-03 | 허버트 지. 버카드 | 고도의 응력완화율을 나타내는 실리콘 밀봉물질(Silicone Sealing Material Exhibiting High Stress Relaxation) |
| US6060546A (en) * | 1996-09-05 | 2000-05-09 | General Electric Company | Non-aqueous silicone emulsions |
| IL125947A0 (en) | 1997-09-17 | 1999-04-11 | American Cyanamid Co | 3-(1,2-benzisothiazol- and isoxazol-5-yl)-2,4(1h,3h)-pyrimidinedione or thione and 3-(1,2-benzisothiazol- and isoxazol-5-yl)-4(3)-pyrimidinone or thione herbicidal agents |
| US6200581B1 (en) | 1999-04-28 | 2001-03-13 | Dow Corning Corporation | Elastomeric silicone terpolymer |
| US6423322B1 (en) * | 1999-05-22 | 2002-07-23 | Wacker Silicones Corporation | Organopolysiloxane gels for use in cosmetics |
| JP2003507551A (ja) * | 1999-08-25 | 2003-02-25 | ゼネラル・エレクトリック・カンパニイ | 極性溶媒と相容性のポリエーテルシロキサンエラストマー |
| US6365670B1 (en) * | 2000-03-10 | 2002-04-02 | Wacker Silicones Corporation | Organopolysiloxane gels for use in cosmetics |
| CN101432341B (zh) * | 2006-03-21 | 2013-03-27 | 陶氏康宁公司 | 硅氧烷有机弹性体凝胶 |
| WO2008057155A1 (en) * | 2006-11-07 | 2008-05-15 | Dow Corning Corporation | Silicone skin adhesive gels |
| KR20090094044A (ko) * | 2006-12-29 | 2009-09-02 | 다우 코닝 코포레이션 | 실리콘 엘라스토머 겔을 함유하는 퍼스널 케어 조성물 |
| KR101519176B1 (ko) * | 2007-06-29 | 2015-05-18 | 다우 코닝 코포레이션 | 폴리알킬옥실렌 가교결합된 실리콘 엘라스토머를 갖는 실리콘-유기 겔 |
| CN102482495B (zh) * | 2009-09-03 | 2014-09-10 | 道康宁公司 | 具有粘液质硅酮液的个人护理组合物 |
| CN101885846B (zh) * | 2010-06-21 | 2012-01-25 | 陈俊光 | 硅油凝胶化制剂弹性体的制造方法 |
| CN102512339B (zh) * | 2011-12-07 | 2013-06-05 | 广州天赐有机硅科技有限公司 | 一种日化用有机硅凝胶组合物及其制备方法 |
| DE102012206209A1 (de) | 2012-04-16 | 2013-10-17 | Wacker Chemie Ag | Organopolysiloxangele |
-
2013
- 2013-12-17 DE DE102013226249.3A patent/DE102013226249A1/de not_active Withdrawn
-
2014
- 2014-12-15 EP EP14821112.1A patent/EP3083766B1/de not_active Not-in-force
- 2014-12-15 CN CN201480069310.7A patent/CN105980448B/zh not_active Expired - Fee Related
- 2014-12-15 WO PCT/EP2014/077804 patent/WO2015091381A1/de not_active Ceased
- 2014-12-15 JP JP2016540643A patent/JP6313451B2/ja active Active
- 2014-12-15 KR KR1020167015968A patent/KR101883580B1/ko not_active Expired - Fee Related
- 2014-12-15 US US15/104,056 patent/US9770403B2/en not_active Expired - Fee Related
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