JPS61249908A - 歯科床用レジン形成用組成物 - Google Patents
歯科床用レジン形成用組成物Info
- Publication number
- JPS61249908A JPS61249908A JP60089697A JP8969785A JPS61249908A JP S61249908 A JPS61249908 A JP S61249908A JP 60089697 A JP60089697 A JP 60089697A JP 8969785 A JP8969785 A JP 8969785A JP S61249908 A JPS61249908 A JP S61249908A
- Authority
- JP
- Japan
- Prior art keywords
- composition
- polymerization
- resin
- forming
- dental
- 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
- 239000000203 mixture Substances 0.000 title claims abstract description 22
- 239000011347 resin Substances 0.000 title claims abstract description 19
- 229920005989 resin Polymers 0.000 title claims abstract description 19
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 32
- 239000003638 chemical reducing agent Substances 0.000 claims abstract description 13
- 239000003112 inhibitor Substances 0.000 claims abstract description 13
- 150000003512 tertiary amines Chemical class 0.000 claims abstract description 10
- 239000002685 polymerization catalyst Substances 0.000 claims abstract description 3
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 abstract description 16
- 239000000178 monomer Substances 0.000 abstract description 10
- 229920000642 polymer Polymers 0.000 abstract description 8
- 238000002156 mixing Methods 0.000 abstract description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 abstract description 4
- CMGDVUCDZOBDNL-UHFFFAOYSA-N 4-methyl-2h-benzotriazole Chemical compound CC1=CC=CC2=NNN=C12 CMGDVUCDZOBDNL-UHFFFAOYSA-N 0.000 abstract description 3
- NWVVVBRKAWDGAB-UHFFFAOYSA-N p-methoxyphenol Chemical compound COC1=CC=C(O)C=C1 NWVVVBRKAWDGAB-UHFFFAOYSA-N 0.000 abstract description 3
- BUUPQKDIAURBJP-UHFFFAOYSA-N sulfinic acid Chemical compound OS=O BUUPQKDIAURBJP-UHFFFAOYSA-N 0.000 abstract description 3
- LRUDIIUSNGCQKF-UHFFFAOYSA-N 5-methyl-1H-benzotriazole Chemical compound C1=C(C)C=CC2=NNN=C21 LRUDIIUSNGCQKF-UHFFFAOYSA-N 0.000 abstract description 2
- 239000002211 L-ascorbic acid Substances 0.000 abstract description 2
- 235000000069 L-ascorbic acid Nutrition 0.000 abstract description 2
- 229960005070 ascorbic acid Drugs 0.000 abstract description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 abstract description 2
- 239000012964 benzotriazole Substances 0.000 abstract description 2
- 239000000463 material Substances 0.000 description 11
- 238000002845 discoloration Methods 0.000 description 8
- 239000003505 polymerization initiator Substances 0.000 description 7
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 5
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 4
- -1 benzoyl peroxide Chemical class 0.000 description 4
- 150000003254 radicals Chemical class 0.000 description 4
- 239000000805 composite resin Substances 0.000 description 3
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 239000000843 powder Substances 0.000 description 3
- 239000000126 substance Substances 0.000 description 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 description 2
- 239000004925 Acrylic resin Substances 0.000 description 2
- 229920000178 Acrylic resin Polymers 0.000 description 2
- 239000004342 Benzoyl peroxide Substances 0.000 description 2
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 2
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 235000019400 benzoyl peroxide Nutrition 0.000 description 2
- 239000004851 dental resin Substances 0.000 description 2
- ZQMIGQNCOMNODD-UHFFFAOYSA-N diacetyl peroxide Chemical compound CC(=O)OOC(C)=O ZQMIGQNCOMNODD-UHFFFAOYSA-N 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 229920001483 poly(ethyl methacrylate) polymer Polymers 0.000 description 2
- 239000001294 propane Substances 0.000 description 2
- VDYWHVQKENANGY-UHFFFAOYSA-N 1,3-Butyleneglycol dimethacrylate Chemical compound CC(=C)C(=O)OC(C)CCOC(=O)C(C)=C VDYWHVQKENANGY-UHFFFAOYSA-N 0.000 description 1
- WFUGQJXVXHBTEM-UHFFFAOYSA-N 2-hydroperoxy-2-(2-hydroperoxybutan-2-ylperoxy)butane Chemical compound CCC(C)(OO)OOC(C)(CC)OO WFUGQJXVXHBTEM-UHFFFAOYSA-N 0.000 description 1
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 description 1
- KATSEUSPUVTAAQ-UHFFFAOYSA-N 2h-benzotriazole;5-methyl-2h-benzotriazole Chemical compound C1=CC=C2NN=NC2=C1.CC1=CC=C2NN=NC2=C1 KATSEUSPUVTAAQ-UHFFFAOYSA-N 0.000 description 1
- DBCAQXHNJOFNGC-UHFFFAOYSA-N 4-bromo-1,1,1-trifluorobutane Chemical compound FC(F)(F)CCCBr DBCAQXHNJOFNGC-UHFFFAOYSA-N 0.000 description 1
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 description 1
- 241000219061 Rheum Species 0.000 description 1
- 235000009411 Rheum rhabarbarum Nutrition 0.000 description 1
- 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 description 1
- ULQMPOIOSDXIGC-UHFFFAOYSA-N [2,2-dimethyl-3-(2-methylprop-2-enoyloxy)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(C)COC(=O)C(C)=C ULQMPOIOSDXIGC-UHFFFAOYSA-N 0.000 description 1
- SWHLOXLFJPTYTL-UHFFFAOYSA-N [2-methyl-3-(2-methylprop-2-enoyloxy)-2-(2-methylprop-2-enoyloxymethyl)propyl] 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(C)(COC(=O)C(C)=C)COC(=O)C(C)=C SWHLOXLFJPTYTL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- UKXSKSHDVLQNKG-UHFFFAOYSA-N benzilic acid Chemical compound C=1C=CC=CC=1C(O)(C(=O)O)C1=CC=CC=C1 UKXSKSHDVLQNKG-UHFFFAOYSA-N 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- SUPCQIBBMFXVTL-UHFFFAOYSA-N ethyl 2-methylprop-2-enoate Chemical compound CCOC(=O)C(C)=C SUPCQIBBMFXVTL-UHFFFAOYSA-N 0.000 description 1
- STVZJERGLQHEKB-UHFFFAOYSA-N ethylene glycol dimethacrylate Substances CC(=C)C(=O)OCCOC(=O)C(C)=C STVZJERGLQHEKB-UHFFFAOYSA-N 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- CIHOLLKRGTVIJN-UHFFFAOYSA-N tert‐butyl hydroperoxide Chemical compound CC(C)(C)OO CIHOLLKRGTVIJN-UHFFFAOYSA-N 0.000 description 1
- 238000012795 verification Methods 0.000 description 1
Landscapes
- Dental Preparations (AREA)
- Polymerization Catalysts (AREA)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60089697A JPS61249908A (ja) | 1985-04-25 | 1985-04-25 | 歯科床用レジン形成用組成物 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP60089697A JPS61249908A (ja) | 1985-04-25 | 1985-04-25 | 歯科床用レジン形成用組成物 |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS61249908A true JPS61249908A (ja) | 1986-11-07 |
| JPH0578531B2 JPH0578531B2 (2) | 1993-10-29 |
Family
ID=13977956
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP60089697A Granted JPS61249908A (ja) | 1985-04-25 | 1985-04-25 | 歯科床用レジン形成用組成物 |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS61249908A (2) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02142711A (ja) * | 1988-11-24 | 1990-05-31 | Jishi Toushi Kogyo Kk | 歯科用樹脂組成物 |
| WO1995022955A1 (en) * | 1994-02-28 | 1995-08-31 | Minnesota Mining And Manufacturing Company | Improved color stability of dental compositions containing metal complexed ascorbic acid |
| US5646216A (en) * | 1992-03-11 | 1997-07-08 | Watson; Sherman L. | Injectable curable composition for making soft resilient interocclusal dental appliance |
| JP2010235536A (ja) * | 2009-03-31 | 2010-10-21 | Kuraray Medical Inc | 歯科用組成物 |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2189147A1 (en) | 2007-09-13 | 2010-05-26 | Sun Medical Co., Ltd. | Dental polymerizable composition and kit therefor |
| JP6153934B2 (ja) | 2012-09-18 | 2017-06-28 | 株式会社ジーシー | 暫間補綴物の作製方法 |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51131199A (en) * | 1975-05-08 | 1976-11-15 | Nakagawa Seikoudou Goumei | Hemorrhoids operational instrument |
| JPS5428339A (en) * | 1977-08-04 | 1979-03-02 | Kuraray Co Ltd | Packaging of adhesives for human hard tissues having improved stability |
| JPS59138203A (ja) * | 1983-01-14 | 1984-08-08 | クルツァ・ゲーエムベーバー | 光重合性組成物及び光重合性組成物の光重合方法 |
-
1985
- 1985-04-25 JP JP60089697A patent/JPS61249908A/ja active Granted
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS51131199A (en) * | 1975-05-08 | 1976-11-15 | Nakagawa Seikoudou Goumei | Hemorrhoids operational instrument |
| JPS5428339A (en) * | 1977-08-04 | 1979-03-02 | Kuraray Co Ltd | Packaging of adhesives for human hard tissues having improved stability |
| JPS59138203A (ja) * | 1983-01-14 | 1984-08-08 | クルツァ・ゲーエムベーバー | 光重合性組成物及び光重合性組成物の光重合方法 |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH02142711A (ja) * | 1988-11-24 | 1990-05-31 | Jishi Toushi Kogyo Kk | 歯科用樹脂組成物 |
| US5646216A (en) * | 1992-03-11 | 1997-07-08 | Watson; Sherman L. | Injectable curable composition for making soft resilient interocclusal dental appliance |
| EP0941732A3 (en) * | 1992-03-11 | 2000-03-29 | WATSON, Sherman L. | Soft resilient interocclusal dental appliance |
| WO1995022955A1 (en) * | 1994-02-28 | 1995-08-31 | Minnesota Mining And Manufacturing Company | Improved color stability of dental compositions containing metal complexed ascorbic acid |
| JP2010235536A (ja) * | 2009-03-31 | 2010-10-21 | Kuraray Medical Inc | 歯科用組成物 |
Also Published As
| Publication number | Publication date |
|---|---|
| JPH0578531B2 (2) | 1993-10-29 |
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