JP2015523415A5 - - Google Patents
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- JP2015523415A5 JP2015523415A5 JP2015501696A JP2015501696A JP2015523415A5 JP 2015523415 A5 JP2015523415 A5 JP 2015523415A5 JP 2015501696 A JP2015501696 A JP 2015501696A JP 2015501696 A JP2015501696 A JP 2015501696A JP 2015523415 A5 JP2015523415 A5 JP 2015523415A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- prepolymer
- hydrogen
- carbon atoms
- composition
- 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.)
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- 239000000203 mixture Substances 0.000 claims 14
- -1 hydrocarbon radicals Chemical class 0.000 claims 13
- 125000004432 carbon atom Chemical group C* 0.000 claims 10
- 229910052739 hydrogen Inorganic materials 0.000 claims 10
- 239000001257 hydrogen Substances 0.000 claims 10
- 239000004215 Carbon black (E152) Substances 0.000 claims 9
- 229930195733 hydrocarbon Natural products 0.000 claims 9
- 125000005842 heteroatom Chemical group 0.000 claims 8
- 239000000178 monomer Substances 0.000 claims 7
- 229910052760 oxygen Inorganic materials 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 150000002431 hydrogen Chemical class 0.000 claims 4
- 229920001296 polysiloxane Polymers 0.000 claims 4
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 3
- 125000004122 cyclic group Chemical group 0.000 claims 3
- 239000000017 hydrogel Substances 0.000 claims 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 3
- 229920002554 vinyl polymer Polymers 0.000 claims 3
- XFCMNSHQOZQILR-UHFFFAOYSA-N 2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOC(=O)C(C)=C XFCMNSHQOZQILR-UHFFFAOYSA-N 0.000 claims 2
- OMIGHNLMNHATMP-UHFFFAOYSA-N 2-hydroxyethyl prop-2-enoate Chemical compound OCCOC(=O)C=C OMIGHNLMNHATMP-UHFFFAOYSA-N 0.000 claims 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims 2
- 150000004945 aromatic hydrocarbons Chemical class 0.000 claims 2
- 230000002209 hydrophobic effect Effects 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 125000005647 linker group Chemical group 0.000 claims 2
- 229920000233 poly(alkylene oxides) Polymers 0.000 claims 2
- 150000003254 radicals Chemical class 0.000 claims 2
- JWYVGKFDLWWQJX-UHFFFAOYSA-N 1-ethenylazepan-2-one Chemical compound C=CN1CCCCCC1=O JWYVGKFDLWWQJX-UHFFFAOYSA-N 0.000 claims 1
- 239000012956 1-hydroxycyclohexylphenyl-ketone Substances 0.000 claims 1
- IGGDKDTUCAWDAN-UHFFFAOYSA-N 1-vinylnaphthalene Chemical compound C1=CC=C2C(C=C)=CC=CC2=C1 IGGDKDTUCAWDAN-UHFFFAOYSA-N 0.000 claims 1
- PIZHFBODNLEQBL-UHFFFAOYSA-N 2,2-diethoxy-1-phenylethanone Chemical compound CCOC(OCC)C(=O)C1=CC=CC=C1 PIZHFBODNLEQBL-UHFFFAOYSA-N 0.000 claims 1
- QRIMLDXJAPZHJE-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CO QRIMLDXJAPZHJE-UHFFFAOYSA-N 0.000 claims 1
- AVTLBBWTUPQRAY-UHFFFAOYSA-N 2-(2-cyanobutan-2-yldiazenyl)-2-methylbutanenitrile Chemical compound CCC(C)(C#N)N=NC(C)(CC)C#N AVTLBBWTUPQRAY-UHFFFAOYSA-N 0.000 claims 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 claims 1
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 claims 1
- WYGWHHGCAGTUCH-UHFFFAOYSA-N 2-[(2-cyano-4-methylpentan-2-yl)diazenyl]-2,4-dimethylpentanenitrile Chemical compound CC(C)CC(C)(C#N)N=NC(C)(C#N)CC(C)C WYGWHHGCAGTUCH-UHFFFAOYSA-N 0.000 claims 1
- BQZJOQXSCSZQPS-UHFFFAOYSA-N 2-methoxy-1,2-diphenylethanone Chemical compound C=1C=CC=CC=1C(OC)C(=O)C1=CC=CC=C1 BQZJOQXSCSZQPS-UHFFFAOYSA-N 0.000 claims 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims 1
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 claims 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 claims 1
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims 1
- 239000004342 Benzoyl peroxide Substances 0.000 claims 1
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 claims 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 claims 1
- NGXMPSHQTWLSBM-UHFFFAOYSA-N CC(=C)C(O)=O.CC(=C)C(O)=O.CC(=C)C(O)=O.O=C=CC(=C=O)C=C=O Chemical compound CC(=C)C(O)=O.CC(=C)C(O)=O.CC(=C)C(O)=O.O=C=CC(=C=O)C=C=O NGXMPSHQTWLSBM-UHFFFAOYSA-N 0.000 claims 1
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims 1
- IMROMDMJAWUWLK-UHFFFAOYSA-N Ethenol Chemical compound OC=C IMROMDMJAWUWLK-UHFFFAOYSA-N 0.000 claims 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical group CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical group C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims 1
- HLJYBXJFKDDIBI-UHFFFAOYSA-N O=[PH2]C(=O)C1=CC=CC=C1 Chemical compound O=[PH2]C(=O)C1=CC=CC=C1 HLJYBXJFKDDIBI-UHFFFAOYSA-N 0.000 claims 1
- 239000002202 Polyethylene glycol Substances 0.000 claims 1
- 239000004721 Polyphenylene oxide Substances 0.000 claims 1
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 150000001336 alkenes Chemical class 0.000 claims 1
- 125000003342 alkenyl group Chemical group 0.000 claims 1
- 150000001412 amines Chemical class 0.000 claims 1
- 239000003125 aqueous solvent Substances 0.000 claims 1
- 125000003710 aryl alkyl group Chemical group 0.000 claims 1
- 125000003118 aryl group Chemical group 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- 235000019400 benzoyl peroxide Nutrition 0.000 claims 1
- MQDJYUACMFCOFT-UHFFFAOYSA-N bis[2-(1-hydroxycyclohexyl)phenyl]methanone Chemical compound C=1C=CC=C(C(=O)C=2C(=CC=CC=2)C2(O)CCCCC2)C=1C1(O)CCCCC1 MQDJYUACMFCOFT-UHFFFAOYSA-N 0.000 claims 1
- QUZSUMLPWDHKCJ-UHFFFAOYSA-N bisphenol A dimethacrylate Chemical compound C1=CC(OC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OC(=O)C(C)=C)C=C1 QUZSUMLPWDHKCJ-UHFFFAOYSA-N 0.000 claims 1
- 239000000872 buffer Substances 0.000 claims 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 238000004587 chromatography analysis Methods 0.000 claims 1
- 238000004140 cleaning Methods 0.000 claims 1
- 238000000576 coating method Methods 0.000 claims 1
- 229920001577 copolymer Polymers 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 claims 1
- 125000000753 cycloalkyl group Chemical group 0.000 claims 1
- KPUWHANPEXNPJT-UHFFFAOYSA-N disiloxane Chemical class [SiH3]O[SiH3] KPUWHANPEXNPJT-UHFFFAOYSA-N 0.000 claims 1
- 239000000839 emulsion Substances 0.000 claims 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 claims 1
- 238000000605 extraction Methods 0.000 claims 1
- 238000009472 formulation Methods 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 229920001519 homopolymer Polymers 0.000 claims 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical class I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 claims 1
- 239000003999 initiator Substances 0.000 claims 1
- 229910017053 inorganic salt Inorganic materials 0.000 claims 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims 1
- 239000010985 leather Substances 0.000 claims 1
- 239000007788 liquid Substances 0.000 claims 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 claims 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims 1
- RQAKESSLMFZVMC-UHFFFAOYSA-N n-ethenylacetamide Chemical compound CC(=O)NC=C RQAKESSLMFZVMC-UHFFFAOYSA-N 0.000 claims 1
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 claims 1
- KYKIFKUTBWKKRE-UHFFFAOYSA-N n-ethenylpropan-2-amine Chemical compound CC(C)NC=C KYKIFKUTBWKKRE-UHFFFAOYSA-N 0.000 claims 1
- QNILTEGFHQSKFF-UHFFFAOYSA-N n-propan-2-ylprop-2-enamide Chemical compound CC(C)NC(=O)C=C QNILTEGFHQSKFF-UHFFFAOYSA-N 0.000 claims 1
- 125000001624 naphthyl group Chemical group 0.000 claims 1
- 239000003973 paint Substances 0.000 claims 1
- 239000000123 paper Substances 0.000 claims 1
- 150000002978 peroxides Chemical class 0.000 claims 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 1
- FAQJJMHZNSSFSM-UHFFFAOYSA-N phenylglyoxylic acid Chemical compound OC(=O)C(=O)C1=CC=CC=C1 FAQJJMHZNSSFSM-UHFFFAOYSA-N 0.000 claims 1
- 229920001484 poly(alkylene) Polymers 0.000 claims 1
- 229920000570 polyether Polymers 0.000 claims 1
- 229920001223 polyethylene glycol Polymers 0.000 claims 1
- 230000000379 polymerizing effect Effects 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 239000012266 salt solution Substances 0.000 claims 1
- 239000002904 solvent Substances 0.000 claims 1
- MDDUHVRJJAFRAU-YZNNVMRBSA-N tert-butyl-[(1r,3s,5z)-3-[tert-butyl(dimethyl)silyl]oxy-5-(2-diphenylphosphorylethylidene)-4-methylidenecyclohexyl]oxy-dimethylsilane Chemical compound C1[C@@H](O[Si](C)(C)C(C)(C)C)C[C@H](O[Si](C)(C)C(C)(C)C)C(=C)\C1=C/CP(=O)(C=1C=CC=CC=1)C1=CC=CC=C1 MDDUHVRJJAFRAU-YZNNVMRBSA-N 0.000 claims 1
- 239000004753 textile Substances 0.000 claims 1
- 150000003573 thiols Chemical class 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims 1
- 0 CINC(C(*)=C(*)*)=O Chemical compound CINC(C(*)=C(*)*)=O 0.000 description 2
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201261614262P | 2012-03-22 | 2012-03-22 | |
| US61/614,262 | 2012-03-22 | ||
| PCT/US2013/029302 WO2013142052A2 (en) | 2012-03-22 | 2013-03-06 | Organo-modified silicone polymers and hydrogels comprising the same |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2015523415A JP2015523415A (ja) | 2015-08-13 |
| JP2015523415A5 true JP2015523415A5 (enExample) | 2017-11-16 |
| JP6429242B2 JP6429242B2 (ja) | 2018-11-28 |
Family
ID=49223438
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015501698A Active JP6227625B2 (ja) | 2012-03-22 | 2013-03-06 | 有機変性シリコーンポリマー |
| JP2015501696A Active JP6429242B2 (ja) | 2012-03-22 | 2013-03-06 | 有機変性シリコーンポリマーおよびそれを含むハイドロゲル |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015501698A Active JP6227625B2 (ja) | 2012-03-22 | 2013-03-06 | 有機変性シリコーンポリマー |
Country Status (9)
| Country | Link |
|---|---|
| US (2) | US9890234B2 (enExample) |
| EP (2) | EP2838955A4 (enExample) |
| JP (2) | JP6227625B2 (enExample) |
| KR (2) | KR20140143194A (enExample) |
| CN (2) | CN104955878B (enExample) |
| AU (1) | AU2013235656A1 (enExample) |
| CA (1) | CA2868170A1 (enExample) |
| IN (2) | IN2014MN01867A (enExample) |
| WO (2) | WO2013142052A2 (enExample) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU2013235656A1 (en) | 2012-03-22 | 2014-10-09 | Momentive Performance Materials Inc. | Organo-modified silicone polymers and hydrogels comprising the same |
| EP2953955B1 (en) | 2013-02-06 | 2018-08-15 | Momentive Performance Materials Inc. | (meth)acryloxy-containing trisiloxane, siloxane-containing polymers and biomedical devices therefrom |
| JP2015078333A (ja) * | 2013-10-18 | 2015-04-23 | 日華化学株式会社 | 硬化性オルガノ変性シリコーン及びその製造方法、並びにコーティング剤及び積層体 |
| JP6037453B2 (ja) * | 2013-11-14 | 2016-12-07 | 信越化学工業株式会社 | 眼科デバイス製造用モノマー |
| US9296764B2 (en) * | 2013-12-10 | 2016-03-29 | Momentive Performance Materials Inc. | Hydrophilic silicone composition |
| US9851472B2 (en) | 2015-03-27 | 2017-12-26 | Momentive Performance Materials Inc. | Silicone-based hydrophilic copolymer and hydrogel compositions comprising the same |
| FR3062209B1 (fr) | 2017-01-25 | 2021-08-27 | Commissariat Energie Atomique | Detecteur optique de particules |
| JP7247095B2 (ja) * | 2017-02-16 | 2023-03-28 | モメンティブ パフォーマンス マテリアルズ インコーポレイテッド | イオン変性シリコーン、組成物、およびそれから形成された医療機器 |
| TWI626253B (zh) | 2017-05-25 | 2018-06-11 | 晶碩光學股份有限公司 | 水溶性矽高聚物、矽水膠組成物、矽水膠鏡片及其製造方法 |
| CN107260655B (zh) * | 2017-06-09 | 2021-03-09 | 金陵科技学院 | 一种维生素e改性的硅基水凝胶隐形眼镜载药体系及其制备方法 |
| JP7102503B2 (ja) * | 2017-07-26 | 2022-07-19 | ベーイプシロンカー ヘミー ゲゼルシャフト ミット ベシュレンクター ハフトゥング | ポリエーテルおよびポリシロキサンセグメントを有するポリマー |
| KR102255536B1 (ko) | 2017-11-30 | 2021-05-25 | 주식회사 엘지에너지솔루션 | 젤 폴리머 전해질용 조성물, 이로부터 제조되는 젤 폴리머 전해질 및 이를 포함하는 리튬 이차 전지 |
| WO2020252773A1 (en) | 2019-06-21 | 2020-12-24 | Dow Silicones Corporation | Thermal conductive silicone composition |
| EP3986967A4 (en) | 2019-06-21 | 2023-01-25 | Dow Silicones Corporation | METHOD OF PREPARING A THIXOTROPIC CURING SILICONE COMPOSITION |
| CN114616052B (zh) * | 2019-11-05 | 2024-09-13 | 株式会社Lg生活健康 | 自然降解性微胶囊及其制备方法 |
| JP7681610B2 (ja) | 2020-02-23 | 2025-05-22 | ダウ シリコーンズ コーポレーション | 光硬化性シリコーン組成物及びその硬化物 |
| CN114103320B (zh) * | 2021-11-24 | 2024-01-19 | 四川中烟工业有限责任公司 | 一种保湿三层材料对雪茄烟微环境湿度调控方面的用途 |
| CN114103281B (zh) * | 2021-11-24 | 2024-01-19 | 四川中烟工业有限责任公司 | 一种保湿的三层材料及其制备方法 |
| CN114015053A (zh) * | 2021-12-03 | 2022-02-08 | 郝建强 | 紫外线固化有机硅离型剂 |
| CN115490805B (zh) * | 2022-09-30 | 2023-08-18 | 郑州轻工业大学 | 一种基于氧化还原反应引发的水凝胶 |
| WO2024242750A1 (en) * | 2023-05-23 | 2024-11-28 | Dow Global Technologies Llc | Silicone - (meth)acrylate - polyether copolymer and synthesis method |
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| CA2739102C (en) * | 2008-11-13 | 2016-06-21 | Novartis Ag | Silicone hydrogel materials with chemically bound wetting agents |
| CA2761218C (en) * | 2009-05-22 | 2016-06-28 | Novartis Ag | Actinically-crosslinkable siloxane-containing copolymers |
| WO2010133680A1 (en) | 2009-05-22 | 2010-11-25 | Novartis Ag | Actinically-crosslinkable siloxane-containing copolymers |
| TWI401263B (zh) | 2009-12-31 | 2013-07-11 | Far Eastern New Century Corp | 增進聚矽氧水膠潤濕性之共聚物、包含其之聚矽氧水膠組成物及由此製得之眼用物件 |
| US10391179B2 (en) * | 2011-03-21 | 2019-08-27 | Momentive Performance Materials Inc. | Organomodified carbosiloxane monomers containing compositions and uses thereof |
| CN102303713B (zh) | 2011-09-02 | 2013-09-25 | 浙江双友物流器械股份有限公司 | 一种快速绞紧器 |
| AU2013235656A1 (en) | 2012-03-22 | 2014-10-09 | Momentive Performance Materials Inc. | Organo-modified silicone polymers and hydrogels comprising the same |
-
2013
- 2013-03-06 AU AU2013235656A patent/AU2013235656A1/en not_active Abandoned
- 2013-03-06 KR KR20147029400A patent/KR20140143194A/ko not_active Withdrawn
- 2013-03-06 CA CA2868170A patent/CA2868170A1/en not_active Abandoned
- 2013-03-06 EP EP13763479.6A patent/EP2838955A4/en active Pending
- 2013-03-06 JP JP2015501698A patent/JP6227625B2/ja active Active
- 2013-03-06 CN CN201380024460.1A patent/CN104955878B/zh active Active
- 2013-03-06 IN IN1867MUN2014 patent/IN2014MN01867A/en unknown
- 2013-03-06 IN IN1866MUN2014 patent/IN2014MN01866A/en unknown
- 2013-03-06 WO PCT/US2013/029302 patent/WO2013142052A2/en not_active Ceased
- 2013-03-06 WO PCT/US2013/029316 patent/WO2013142055A2/en not_active Ceased
- 2013-03-06 CN CN201380024477.7A patent/CN105518058B/zh active Active
- 2013-03-06 JP JP2015501696A patent/JP6429242B2/ja active Active
- 2013-03-06 EP EP13764947.1A patent/EP2828338A4/en active Pending
- 2013-03-06 KR KR20147029338A patent/KR20140134715A/ko not_active Withdrawn
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2014
- 2014-09-22 US US14/492,646 patent/US9890234B2/en active Active
- 2014-09-22 US US14/492,378 patent/US9944742B2/en active Active
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