GB1575873A - Photopolymerizable compositions based on acrylic or methaccrylic acid esters - Google Patents
Photopolymerizable compositions based on acrylic or methaccrylic acid esters Download PDFInfo
- Publication number
- GB1575873A GB1575873A GB10352/78A GB1035278A GB1575873A GB 1575873 A GB1575873 A GB 1575873A GB 10352/78 A GB10352/78 A GB 10352/78A GB 1035278 A GB1035278 A GB 1035278A GB 1575873 A GB1575873 A GB 1575873A
- Authority
- GB
- United Kingdom
- Prior art keywords
- photopolymerizable composition
- acrylic
- monoketal
- weight
- ester 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.)
- Expired
Links
- 239000000203 mixture Substances 0.000 title claims description 38
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 title claims description 15
- 150000002148 esters Chemical class 0.000 title description 4
- 239000002253 acid Substances 0.000 title 1
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 19
- -1 methacrylic acid ester compound Chemical class 0.000 claims description 16
- 125000003118 aryl group Chemical group 0.000 claims description 11
- 239000003999 initiator Substances 0.000 claims description 11
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical group C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 claims description 9
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 claims description 8
- NMAKPIATXQEXBT-UHFFFAOYSA-N didecyl phenyl phosphite Chemical group CCCCCCCCCCOP(OCCCCCCCCCC)OC1=CC=CC=C1 NMAKPIATXQEXBT-UHFFFAOYSA-N 0.000 claims description 6
- 125000001931 aliphatic group Chemical group 0.000 claims description 5
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- KUMNEOGIHFCNQW-UHFFFAOYSA-N diphenyl phosphite Chemical compound C=1C=CC=CC=1OP([O-])OC1=CC=CC=C1 KUMNEOGIHFCNQW-UHFFFAOYSA-N 0.000 claims description 3
- BDZBKCUKTQZUTL-UHFFFAOYSA-N triethyl phosphite Chemical compound CCOP(OCC)OCC BDZBKCUKTQZUTL-UHFFFAOYSA-N 0.000 claims description 3
- OKKRPWIIYQTPQF-UHFFFAOYSA-N Trimethylolpropane trimethacrylate Chemical compound CC(=C)C(=O)OCC(CC)(COC(=O)C(C)=C)COC(=O)C(C)=C OKKRPWIIYQTPQF-UHFFFAOYSA-N 0.000 claims description 2
- YYPNJNDODFVZLE-UHFFFAOYSA-N 3-methylbut-2-enoic acid Chemical compound CC(C)=CC(O)=O YYPNJNDODFVZLE-UHFFFAOYSA-N 0.000 claims 1
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 claims 1
- 239000003795 chemical substances by application Substances 0.000 claims 1
- 238000006116 polymerization reaction Methods 0.000 description 19
- 150000001875 compounds Chemical class 0.000 description 7
- 239000000178 monomer Substances 0.000 description 7
- AQSJGOWTSHOLKH-UHFFFAOYSA-N phosphite(3-) Chemical class [O-]P([O-])[O-] AQSJGOWTSHOLKH-UHFFFAOYSA-N 0.000 description 7
- 238000000034 method Methods 0.000 description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 239000006059 cover glass Substances 0.000 description 5
- XYFCBTPGUUZFHI-UHFFFAOYSA-N Phosphine Chemical compound P XYFCBTPGUUZFHI-UHFFFAOYSA-N 0.000 description 4
- 239000012190 activator Substances 0.000 description 4
- ISAOCJYIOMOJEB-UHFFFAOYSA-N desyl alcohol Natural products C=1C=CC=CC=1C(O)C(=O)C1=CC=CC=C1 ISAOCJYIOMOJEB-UHFFFAOYSA-N 0.000 description 4
- 125000005594 diketone group Chemical group 0.000 description 4
- JHPBZFOKBAGZBL-UHFFFAOYSA-N (3-hydroxy-2,2,4-trimethylpentyl) 2-methylprop-2-enoate Chemical compound CC(C)C(O)C(C)(C)COC(=O)C(C)=C JHPBZFOKBAGZBL-UHFFFAOYSA-N 0.000 description 3
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 230000004913 activation Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 230000005855 radiation Effects 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- HVLLSGMXQDNUAL-UHFFFAOYSA-N triphenyl phosphite Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)OC1=CC=CC=C1 HVLLSGMXQDNUAL-UHFFFAOYSA-N 0.000 description 3
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 2
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 2
- 241000183024 Populus tremula Species 0.000 description 2
- 244000028419 Styrax benzoin Species 0.000 description 2
- 235000000126 Styrax benzoin Nutrition 0.000 description 2
- 235000008411 Sumatra benzointree Nutrition 0.000 description 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 description 2
- 150000001241 acetals Chemical class 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229960002130 benzoin Drugs 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000000945 filler Substances 0.000 description 2
- 235000019382 gum benzoic Nutrition 0.000 description 2
- 238000004519 manufacturing process Methods 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 description 2
- 229910000073 phosphorus hydride Inorganic materials 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 235000012239 silicon dioxide Nutrition 0.000 description 2
- 239000000377 silicon dioxide Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- RIOQSEWOXXDEQQ-UHFFFAOYSA-N triphenylphosphine Chemical compound C1=CC=CC=C1P(C=1C=CC=CC=1)C1=CC=CC=C1 RIOQSEWOXXDEQQ-UHFFFAOYSA-N 0.000 description 2
- 230000001133 acceleration Effects 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000004020 conductor Substances 0.000 description 1
- 229940120693 copper naphthenate Drugs 0.000 description 1
- SEVNKWFHTNVOLD-UHFFFAOYSA-L copper;3-(4-ethylcyclohexyl)propanoate;3-(3-ethylcyclopentyl)propanoate Chemical compound [Cu+2].CCC1CCC(CCC([O-])=O)C1.CCC1CCC(CCC([O-])=O)CC1 SEVNKWFHTNVOLD-UHFFFAOYSA-L 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- CZHYKKAKFWLGJO-UHFFFAOYSA-N dimethyl phosphite Chemical compound COP([O-])OC CZHYKKAKFWLGJO-UHFFFAOYSA-N 0.000 description 1
- XMQYIPNJVLNWOE-UHFFFAOYSA-N dioctyl hydrogen phosphite Chemical compound CCCCCCCCOP(O)OCCCCCCCC XMQYIPNJVLNWOE-UHFFFAOYSA-N 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 230000000977 initiatory effect Effects 0.000 description 1
- 230000001678 irradiating effect Effects 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 230000002045 lasting effect Effects 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 150000003018 phosphorus compounds Chemical class 0.000 description 1
- DOIRQSBPFJWKBE-UHFFFAOYSA-N phthalic acid di-n-butyl ester Natural products CCCCOC(=O)C1=CC=CC=C1C(=O)OCCCC DOIRQSBPFJWKBE-UHFFFAOYSA-N 0.000 description 1
- 229920000058 polyacrylate Polymers 0.000 description 1
- 229920001225 polyester resin Polymers 0.000 description 1
- 239000004645 polyester resin Substances 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 239000000523 sample Substances 0.000 description 1
- 238000004904 shortening Methods 0.000 description 1
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical compound O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- TUQOTMZNTHZOKS-UHFFFAOYSA-N tributylphosphine Chemical compound CCCCP(CCCC)CCCC TUQOTMZNTHZOKS-UHFFFAOYSA-N 0.000 description 1
- CYTQBVOFDCPGCX-UHFFFAOYSA-N trimethyl phosphite Chemical compound COP(OC)OC CYTQBVOFDCPGCX-UHFFFAOYSA-N 0.000 description 1
- CNUJLMSKURPSHE-UHFFFAOYSA-N trioctadecyl phosphite Chemical compound CCCCCCCCCCCCCCCCCCOP(OCCCCCCCCCCCCCCCCCC)OCCCCCCCCCCCCCCCCCC CNUJLMSKURPSHE-UHFFFAOYSA-N 0.000 description 1
- QOQNJVLFFRMJTQ-UHFFFAOYSA-N trioctyl phosphite Chemical compound CCCCCCCCOP(OCCCCCCCC)OCCCCCCCC QOQNJVLFFRMJTQ-UHFFFAOYSA-N 0.000 description 1
- QOPBTFMUVTXWFF-UHFFFAOYSA-N tripropyl phosphite Chemical compound CCCOP(OCCC)OCCC QOPBTFMUVTXWFF-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F2/00—Processes of polymerisation
- C08F2/46—Polymerisation initiated by wave energy or particle radiation
- C08F2/48—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light
- C08F2/50—Polymerisation initiated by wave energy or particle radiation by ultraviolet or visible light with sensitising agents
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Polymerisation Methods In General (AREA)
- Dental Preparations (AREA)
- Paints Or Removers (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| CH327877A CH611633A5 (US08092553-20120110-C00004.png) | 1977-03-16 | 1977-03-16 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1575873A true GB1575873A (en) | 1980-10-01 |
Family
ID=4252519
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB10352/78A Expired GB1575873A (en) | 1977-03-16 | 1978-03-15 | Photopolymerizable compositions based on acrylic or methaccrylic acid esters |
Country Status (10)
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2180247A (en) * | 1985-09-11 | 1987-03-25 | G C Dental Ind Corp | Light curing compositions for dental restoration |
| US4804690A (en) * | 1985-09-11 | 1989-02-14 | G-C Dental Industrial Corporation | Light curing compositions for dental restoration |
| US4843110A (en) * | 1985-09-11 | 1989-06-27 | G-C Dental Industrial Corporation | Light curing compositions for dental restoration |
| US10221193B2 (en) | 2010-01-18 | 2019-03-05 | Lintfiled Limited | Photoinitiated reactions |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB1569021A (en) * | 1976-03-17 | 1980-06-11 | Kuraray Co | Adhesive cementing agents containing partial phosphonic orphosphonic acid esters |
| US4252526A (en) * | 1979-05-24 | 1981-02-24 | Sybron Corporation | Barium aluminum silicate filler for U.V. curable composites |
| US4525256A (en) * | 1983-07-01 | 1985-06-25 | Johnson & Johnson Dental Products Company | Photopolymerizable composition including catalyst comprising diketone plus 4-(N,N-dimethylamino)benzoic acid or ester thereof |
| US4816496A (en) * | 1984-06-26 | 1989-03-28 | Kabushiki Kaisha Toshiba | Photocurable composition |
| US4657941A (en) * | 1984-11-29 | 1987-04-14 | Dentsply Research & Development Corp. | Biologically compatible adhesive containing a phosphorus adhesion promoter and a sulfinic accelerator |
| DE3676054D1 (de) * | 1985-05-17 | 1991-01-17 | Atochem North America | Durch waessriges alkali entwickelbare, uv-haertbare urethanacrylatverbindungen und zusammensetzungen, die zur herstellung von beschichtung fuer loetmasken geeignet sind. |
| US4814423A (en) * | 1987-11-06 | 1989-03-21 | Dentsply Research & Development Corp. | Dual bonding adhesive composition |
| US5362769A (en) * | 1992-05-07 | 1994-11-08 | Ormco Corporation | Orthodontic adhesives |
| JP3442776B2 (ja) * | 1992-12-21 | 2003-09-02 | 株式会社アーデル | 可視光重合型接着剤用光重合開始剤組成物 |
| TW414713B (en) * | 1994-05-12 | 2000-12-11 | Dentsply Gmbh | Fluoride releasing liquid dental primer product and method |
| IE980775A1 (en) * | 1998-09-17 | 2000-03-22 | Loctite R & D Ltd | Auto-oxidation systems for air-activatable polymerisable compositions |
| US6803394B2 (en) * | 1999-12-17 | 2004-10-12 | Gel Products, Inc. | Radiation curable nail coatings and artificial nail tips and methods of using same |
| US6391938B1 (en) | 1999-12-17 | 2002-05-21 | Gel Products, Inc. | Radiation curable nail coatings |
| US6481444B1 (en) | 1999-12-17 | 2002-11-19 | Gel Products, Inc. | Finishing compounds for radiation curable nail coatings |
| US20040087687A1 (en) * | 2002-10-30 | 2004-05-06 | Vantico A&T Us Inc. | Photocurable compositions with phosphite viscosity stabilizers |
| JP4747251B2 (ja) * | 2003-08-22 | 2011-08-17 | サートーマー・テクノロジー・ユーエスエイ・リミテッド・ライアビリティ・カンパニー | Ｕｖ系の高温安定化 |
| JP5756604B2 (ja) | 2009-07-21 | 2015-07-29 | リー ヘイル ダニー | ネイル用の除去可能なゲル適用向けの組成物、及びそれらの使用方法 |
| US8263677B2 (en) * | 2009-09-08 | 2012-09-11 | Creative Nail Design, Inc. | Removable color gel basecoat for artificial nail coatings and methods therefore |
| US8492454B2 (en) * | 2009-10-05 | 2013-07-23 | Creative Nail Design, Inc. | Removable color layer for artificial nail coatings and methods therefore |
| US8541482B2 (en) * | 2009-10-05 | 2013-09-24 | Creative Nail Design, Inc. | Removable multilayer nail coating system and methods therefore |
| CN103501755A (zh) | 2011-03-07 | 2014-01-08 | 创意指甲设计公司 | 用于可uv固化的化妆品指甲涂层的组合物和方法 |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3699022A (en) * | 1970-02-05 | 1972-10-17 | Reichhold Albert Chemie Ag | Photopolymerizable unsaturated polyesters containing benzoin-ether,organic acid ester,organic phosphine initiators |
| FR2120275A5 (US08092553-20120110-C00004.png) * | 1970-12-28 | 1972-08-18 | Progil | |
| DE2104985C3 (de) * | 1971-02-03 | 1975-05-07 | Passavant-Werke Michelbacher Huette, 6209 Aarbergen | Vorrichtung zur Belüftung von Abwässern oder dergleichen Flüssigkeiten mit einem Belüftungsbecken und mindestens einem Oberflächenbelüfter |
| DE2232365C2 (de) * | 1972-07-01 | 1982-06-09 | Basf Ag, 6700 Ludwigshafen | Durch UV-Bestrahlung polymerisierbare Gemische |
| FI60194C (fi) * | 1972-07-28 | 1981-12-10 | Ciba Geigy Ag | Foerfarande foer framstaellning av bensil-monoketaler |
-
1977
- 1977-03-16 CH CH327877A patent/CH611633A5/xx not_active IP Right Cessation
-
1978
- 1978-03-14 DE DE19782811039 patent/DE2811039A1/de not_active Withdrawn
- 1978-03-15 AT AT184478A patent/AT357761B/de not_active IP Right Cessation
- 1978-03-15 SE SE7803001A patent/SE424641B/sv not_active IP Right Cessation
- 1978-03-15 US US05/886,779 patent/US4189365A/en not_active Expired - Lifetime
- 1978-03-15 JP JP2877478A patent/JPS53113881A/ja active Pending
- 1978-03-15 GB GB10352/78A patent/GB1575873A/en not_active Expired
- 1978-03-15 FR FR7807466A patent/FR2383974A2/fr active Granted
- 1978-03-15 NL NL7802801A patent/NL7802801A/xx not_active Application Discontinuation
- 1978-03-15 CA CA000298995A patent/CA1121548A/en not_active Expired
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2180247A (en) * | 1985-09-11 | 1987-03-25 | G C Dental Ind Corp | Light curing compositions for dental restoration |
| US4771084A (en) * | 1985-09-11 | 1988-09-13 | G-C Dental Industrial Corp. | Light curing compositions for dental restoration |
| US4804690A (en) * | 1985-09-11 | 1989-02-14 | G-C Dental Industrial Corporation | Light curing compositions for dental restoration |
| US4843110A (en) * | 1985-09-11 | 1989-06-27 | G-C Dental Industrial Corporation | Light curing compositions for dental restoration |
| GB2180247B (en) * | 1985-09-11 | 1990-04-04 | G C Dental Ind Corp | Light curing compositions for dental restoration |
| US10221193B2 (en) | 2010-01-18 | 2019-03-05 | Lintfiled Limited | Photoinitiated reactions |
| US10919909B2 (en) | 2010-01-18 | 2021-02-16 | Lintfield Limited | Photoinitiated reactions |
Also Published As
| Publication number | Publication date |
|---|---|
| SE424641B (sv) | 1982-08-02 |
| CH611633A5 (US08092553-20120110-C00004.png) | 1979-06-15 |
| US4189365A (en) | 1980-02-19 |
| CA1121548A (en) | 1982-04-06 |
| SE7803001L (sv) | 1978-09-17 |
| DE2811039A1 (de) | 1978-10-05 |
| AT357761B (de) | 1980-07-25 |
| JPS53113881A (en) | 1978-10-04 |
| NL7802801A (nl) | 1978-09-19 |
| FR2383974A2 (fr) | 1978-10-13 |
| FR2383974B1 (US08092553-20120110-C00004.png) | 1985-04-05 |
| ATA184478A (de) | 1979-12-15 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PS | Patent sealed [section 19, patents act 1949] | ||
| PCNP | Patent ceased through non-payment of renewal fee |