JP2001220394A5 - - Google Patents
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- Publication number
- JP2001220394A5 JP2001220394A5 JP2000029164A JP2000029164A JP2001220394A5 JP 2001220394 A5 JP2001220394 A5 JP 2001220394A5 JP 2000029164 A JP2000029164 A JP 2000029164A JP 2000029164 A JP2000029164 A JP 2000029164A JP 2001220394 A5 JP2001220394 A5 JP 2001220394A5
- Authority
- JP
- Japan
- Prior art keywords
- group
- formula
- hydroxypropyl
- glycidoxypropyl
- 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.)
- Granted
Links
- -1 glycidoxypropyl group Chemical group 0.000 description 68
- 150000001875 compounds Chemical class 0.000 description 14
- 239000000178 monomer Substances 0.000 description 9
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 8
- 125000004432 carbon atom Chemical group C* 0.000 description 7
- CREMABGTGYGIQB-UHFFFAOYSA-N carbon carbon Chemical compound C.C CREMABGTGYGIQB-UHFFFAOYSA-N 0.000 description 6
- 239000011203 carbon fibre reinforced carbon Substances 0.000 description 6
- 229910052760 oxygen Inorganic materials 0.000 description 6
- 229920000642 polymer Polymers 0.000 description 6
- VVJKKWFAADXIJK-UHFFFAOYSA-N Allylamine Chemical compound NCC=C VVJKKWFAADXIJK-UHFFFAOYSA-N 0.000 description 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 4
- 239000001301 oxygen Substances 0.000 description 4
- 230000035699 permeability Effects 0.000 description 4
- 238000006116 polymerization reaction Methods 0.000 description 4
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 3
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
- 230000000704 physical effect Effects 0.000 description 3
- 125000001424 substituent group Chemical group 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 125000000547 substituted alkyl group Chemical group 0.000 description 2
- 125000003107 substituted aryl group Chemical group 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 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 1
- DIOZVWSHACHNRT-UHFFFAOYSA-N 2-(2-prop-2-enoxyethoxy)ethanol Chemical compound OCCOCCOCC=C DIOZVWSHACHNRT-UHFFFAOYSA-N 0.000 description 1
- PFUXCENAHWMURC-UHFFFAOYSA-N 2-[2-(2-prop-2-enoxyethoxy)ethoxy]ethanol Chemical compound OCCOCCOCCOCC=C PFUXCENAHWMURC-UHFFFAOYSA-N 0.000 description 1
- HWSSEYVMGDIFMH-UHFFFAOYSA-N 2-[2-[2-(2-methylprop-2-enoyloxy)ethoxy]ethoxy]ethyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCOCCOCCOC(=O)C(C)=C HWSSEYVMGDIFMH-UHFFFAOYSA-N 0.000 description 1
- XMLYCEVDHLAQEL-UHFFFAOYSA-N 2-hydroxy-2-methyl-1-phenylpropan-1-one Chemical compound CC(C)(O)C(=O)C1=CC=CC=C1 XMLYCEVDHLAQEL-UHFFFAOYSA-N 0.000 description 1
- BESKSSIEODQWBP-UHFFFAOYSA-N 3-tris(trimethylsilyloxy)silylpropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCC[Si](O[Si](C)(C)C)(O[Si](C)(C)C)O[Si](C)(C)C BESKSSIEODQWBP-UHFFFAOYSA-N 0.000 description 1
- WSSSPWUEQFSQQG-UHFFFAOYSA-N 4-methyl-1-pentene Chemical compound CC(C)CC=C WSSSPWUEQFSQQG-UHFFFAOYSA-N 0.000 description 1
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 description 1
- 241000238631 Hexapoda Species 0.000 description 1
- 235000002597 Solanum melongena Nutrition 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000003277 amino group Chemical group 0.000 description 1
- 239000012300 argon atmosphere Substances 0.000 description 1
- 125000003710 aryl alkyl group Chemical group 0.000 description 1
- 125000003118 aryl group Chemical group 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000007809 chemical reaction catalyst Substances 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 125000003700 epoxy group Chemical group 0.000 description 1
- 150000004687 hexahydrates Chemical class 0.000 description 1
- 238000006459 hydrosilylation reaction Methods 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000000203 mixture Substances 0.000 description 1
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 238000000425 proton nuclear magnetic resonance spectrum Methods 0.000 description 1
- 238000000746 purification Methods 0.000 description 1
- 238000010992 reflux Methods 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 238000010898 silica gel chromatography Methods 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Priority Applications (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000029164A JP4524838B2 (ja) | 2000-02-07 | 2000-02-07 | 眼用レンズ |
| US10/486,263 US20040198938A1 (en) | 2000-02-07 | 2001-08-06 | Monomers, polymers and ophthalmic lenses |
| PCT/JP2001/006741 WO2003027123A1 (fr) | 2000-02-07 | 2001-08-06 | Monomeres, polymeres et lentilles ophtalmologiques |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2000029164A JP4524838B2 (ja) | 2000-02-07 | 2000-02-07 | 眼用レンズ |
| PCT/JP2001/006741 WO2003027123A1 (fr) | 2000-02-07 | 2001-08-06 | Monomeres, polymeres et lentilles ophtalmologiques |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2001220394A JP2001220394A (ja) | 2001-08-14 |
| JP2001220394A5 true JP2001220394A5 (enExample) | 2007-03-29 |
| JP4524838B2 JP4524838B2 (ja) | 2010-08-18 |
Family
ID=26345124
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2000029164A Expired - Lifetime JP4524838B2 (ja) | 2000-02-07 | 2000-02-07 | 眼用レンズ |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US20040198938A1 (enExample) |
| JP (1) | JP4524838B2 (enExample) |
Families Citing this family (20)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6822016B2 (en) | 2001-09-10 | 2004-11-23 | Johnson & Johnson Vision Care, Inc. | Biomedical devices containing internal wetting agents |
| EP1424339A4 (en) * | 2001-08-06 | 2006-08-02 | Johson & Johnson Vision Care I | MONOMERS, POLYMERS AND OPHTHALMIC LENSES |
| DK1445641T3 (da) * | 2001-08-28 | 2008-02-04 | Johnson & Johnson Vision Care | Okulære linser |
| US20070138692A1 (en) * | 2002-09-06 | 2007-06-21 | Ford James D | Process for forming clear, wettable silicone hydrogel articles |
| JP4195352B2 (ja) | 2003-09-10 | 2008-12-10 | 三星エスディアイ株式会社 | 発光素子基板およびそれを用いた発光素子 |
| US8053539B2 (en) * | 2006-06-30 | 2011-11-08 | Johnson & Johnson Vision Care Inc. | Siloxanyl materials for molded plastics |
| US8569538B2 (en) * | 2006-06-30 | 2013-10-29 | Johnson & Johnson Vision Care, Inc. | Acryloyl materials for molded plastics |
| JP4899757B2 (ja) * | 2006-09-29 | 2012-03-21 | 東レ株式会社 | 眼用レンズ |
| US20080081850A1 (en) * | 2006-09-29 | 2008-04-03 | Kazuhiko Fujisawa | Process for producing hydrolysis-resistant silicone compounds |
| US7838698B2 (en) | 2006-09-29 | 2010-11-23 | Johnson & Johnson Vision Care, Inc. | Hydrolysis-resistant silicone compounds |
| US9056880B2 (en) | 2006-09-29 | 2015-06-16 | Johnson & Johnson Vision Care, Inc. | Process for producing hydrolysis-resistant silicone compounds |
| US20080119627A1 (en) * | 2006-11-22 | 2008-05-22 | Masataka Nakamura | Methods for purifying siloxanyl monomers |
| US8080622B2 (en) * | 2007-06-29 | 2011-12-20 | Johnson & Johnson Vision Care, Inc. | Soluble silicone prepolymers |
| US7897654B2 (en) * | 2007-12-27 | 2011-03-01 | Johnson & Johnson Vision Care Inc. | Silicone prepolymer solutions |
| JP4671309B1 (ja) * | 2010-06-28 | 2011-04-13 | アイカ工業株式会社 | 付加型シリコーン樹脂組成物 |
| JP6037454B2 (ja) * | 2013-11-15 | 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 |
| JP6356635B2 (ja) * | 2014-06-12 | 2018-07-11 | 信越化学工業株式会社 | 眼科デバイス製造用モノマー |
| JP6173260B2 (ja) * | 2014-06-12 | 2017-08-02 | 信越化学工業株式会社 | 眼科デバイス製造用モノマー |
| JP6826189B2 (ja) * | 2017-03-29 | 2021-02-03 | 信越化学工業株式会社 | （メタ）アクリル変性シリコーンマクロモノマー |
| JP6800107B2 (ja) * | 2017-08-01 | 2020-12-16 | 信越化学工業株式会社 | シロキサン化合物及びその製造方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS584327B2 (ja) * | 1978-07-15 | 1983-01-26 | 東洋コンタクトレンズ株式会社 | コンタクトレンズ |
| JPS61281116A (ja) * | 1985-06-07 | 1986-12-11 | Nippon Contact Lens:Kk | コンタクトレンズ材料 |
| DE3729457A1 (de) * | 1987-09-03 | 1989-03-16 | Bayer Ag | Kontaktoptische gegenstaende |
| JP2774233B2 (ja) * | 1992-08-26 | 1998-07-09 | 株式会社メニコン | 眼用レンズ材料 |
| JPH06214197A (ja) * | 1993-01-18 | 1994-08-05 | Seiko Epson Corp | ソフトコンタクトレンズ |
| TW243455B (enExample) * | 1993-02-09 | 1995-03-21 | Ciba Geigy | |
| JPH1072525A (ja) * | 1996-06-25 | 1998-03-17 | Toray Ind Inc | プラスチック成形品 |
| JP3799374B2 (ja) * | 1997-09-01 | 2006-07-19 | 株式会社トクヤマ | 接着性組成物 |
| US5959117A (en) * | 1998-08-10 | 1999-09-28 | Bausch & Lomb | Monomers useful for contact lens materials |
-
2000
- 2000-02-07 JP JP2000029164A patent/JP4524838B2/ja not_active Expired - Lifetime
-
2001
- 2001-08-06 US US10/486,263 patent/US20040198938A1/en not_active Abandoned
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