JP2016509057A5 - - Google Patents
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- JP2016509057A5 JP2016509057A5 JP2015558933A JP2015558933A JP2016509057A5 JP 2016509057 A5 JP2016509057 A5 JP 2016509057A5 JP 2015558933 A JP2015558933 A JP 2015558933A JP 2015558933 A JP2015558933 A JP 2015558933A JP 2016509057 A5 JP2016509057 A5 JP 2016509057A5
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- Prior art keywords
- component
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- Prior art date
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- 239000000203 mixture Substances 0.000 claims 17
- 239000003381 stabilizer Substances 0.000 claims 7
- 125000004432 carbon atom Chemical group C* 0.000 claims 6
- 239000003054 catalyst Substances 0.000 claims 6
- 150000001875 compounds Chemical class 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 4
- 229920000642 polymer Polymers 0.000 claims 4
- 229920001296 polysiloxane Polymers 0.000 claims 4
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 3
- 239000003963 antioxidant agent Substances 0.000 claims 3
- 235000006708 antioxidants Nutrition 0.000 claims 3
- 125000003118 aryl group Chemical group 0.000 claims 3
- 239000003795 chemical substances by application Substances 0.000 claims 3
- 239000000945 filler Substances 0.000 claims 3
- QHGSGZLLHBKSAH-UHFFFAOYSA-N hydridosilicon Chemical group [SiH] QHGSGZLLHBKSAH-UHFFFAOYSA-N 0.000 claims 3
- 239000001257 hydrogen Substances 0.000 claims 3
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims 2
- OPLCSTZDXXUYDU-UHFFFAOYSA-N 2,4-dimethyl-6-tert-butylphenol Chemical compound CC1=CC(C)=C(O)C(C(C)(C)C)=C1 OPLCSTZDXXUYDU-UHFFFAOYSA-N 0.000 claims 2
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims 2
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 claims 2
- 230000003078 antioxidant effect Effects 0.000 claims 2
- 229910052906 cristobalite Inorganic materials 0.000 claims 2
- 238000004132 cross linking Methods 0.000 claims 2
- FSWDLYNGJBGFJH-UHFFFAOYSA-N n,n'-di-2-butyl-1,4-phenylenediamine Chemical compound CCC(C)NC1=CC=C(NC(C)CC)C=C1 FSWDLYNGJBGFJH-UHFFFAOYSA-N 0.000 claims 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical group OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 2
- 229910000077 silane Inorganic materials 0.000 claims 2
- -1 silane compound Chemical class 0.000 claims 2
- 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 claims 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 claims 1
- VNQNXQYZMPJLQX-UHFFFAOYSA-N 1,3,5-tris[(3,5-ditert-butyl-4-hydroxyphenyl)methyl]-1,3,5-triazinane-2,4,6-trione Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CN2C(N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C(=O)N(CC=3C=C(C(O)=C(C=3)C(C)(C)C)C(C)(C)C)C2=O)=O)=C1 VNQNXQYZMPJLQX-UHFFFAOYSA-N 0.000 claims 1
- QJCTXKQREPXYTL-UHFFFAOYSA-N 2,6-ditert-butyl-3-(2,4-ditert-butyl-3-hydroxyphenyl)phenol Chemical group CC(C)(C)c1ccc(-c2ccc(c(O)c2C(C)(C)C)C(C)(C)C)c(c1O)C(C)(C)C QJCTXKQREPXYTL-UHFFFAOYSA-N 0.000 claims 1
- MAKZUCXUISYVIE-UHFFFAOYSA-N 2,6-ditert-butyl-4-methylphenol;2,6-ditert-butylphenol Chemical compound CC(C)(C)C1=CC=CC(C(C)(C)C)=C1O.CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 MAKZUCXUISYVIE-UHFFFAOYSA-N 0.000 claims 1
- XQESJWNDTICJHW-UHFFFAOYSA-N 2-[(2-hydroxy-5-methyl-3-nonylphenyl)methyl]-4-methyl-6-nonylphenol Chemical compound CCCCCCCCCC1=CC(C)=CC(CC=2C(=C(CCCCCCCCC)C=C(C)C=2)O)=C1O XQESJWNDTICJHW-UHFFFAOYSA-N 0.000 claims 1
- PFANXOISJYKQRP-UHFFFAOYSA-N 2-tert-butyl-4-[1-(5-tert-butyl-4-hydroxy-2-methylphenyl)butyl]-5-methylphenol Chemical compound C=1C(C(C)(C)C)=C(O)C=C(C)C=1C(CCC)C1=CC(C(C)(C)C)=C(O)C=C1C PFANXOISJYKQRP-UHFFFAOYSA-N 0.000 claims 1
- ZDRSNHRWLQQICP-UHFFFAOYSA-N 2-tert-butyl-4-[2-(3-tert-butyl-4-hydroxyphenyl)propan-2-yl]phenol Chemical compound C1=C(O)C(C(C)(C)C)=CC(C(C)(C)C=2C=C(C(O)=CC=2)C(C)(C)C)=C1 ZDRSNHRWLQQICP-UHFFFAOYSA-N 0.000 claims 1
- 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 claims 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims 1
- YCKRFDGAMUMZLT-UHFFFAOYSA-N Fluorine atom Chemical compound [F] YCKRFDGAMUMZLT-UHFFFAOYSA-N 0.000 claims 1
- CFXCGWWYIDZIMU-UHFFFAOYSA-N Octyl-3,5-di-tert-butyl-4-hydroxy-hydrocinnamate Chemical compound CCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 CFXCGWWYIDZIMU-UHFFFAOYSA-N 0.000 claims 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims 1
- 229930003427 Vitamin E Natural products 0.000 claims 1
- 238000007259 addition reaction Methods 0.000 claims 1
- 239000000654 additive Substances 0.000 claims 1
- 125000001931 aliphatic group Chemical group 0.000 claims 1
- 125000002877 alkyl aryl group Chemical group 0.000 claims 1
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 125000002947 alkylene group Chemical group 0.000 claims 1
- 125000003277 amino group Chemical group 0.000 claims 1
- SXXILWLQSQDLDL-UHFFFAOYSA-N bis(8-methylnonyl) phenyl phosphite Chemical compound CC(C)CCCCCCCOP(OCCCCCCCC(C)C)OC1=CC=CC=C1 SXXILWLQSQDLDL-UHFFFAOYSA-N 0.000 claims 1
- 235000010354 butylated hydroxytoluene Nutrition 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 239000003431 cross linking reagent Substances 0.000 claims 1
- 239000006185 dispersion Substances 0.000 claims 1
- HQQADJVZYDDRJT-UHFFFAOYSA-N ethene;prop-1-ene Chemical group C=C.CC=C HQQADJVZYDDRJT-UHFFFAOYSA-N 0.000 claims 1
- 229910052731 fluorine Inorganic materials 0.000 claims 1
- 239000011737 fluorine Substances 0.000 claims 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 claims 1
- 229910052736 halogen Inorganic materials 0.000 claims 1
- 125000005843 halogen group Chemical group 0.000 claims 1
- 150000002367 halogens Chemical class 0.000 claims 1
- 125000001183 hydrocarbyl group Chemical group 0.000 claims 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 1
- 239000004615 ingredient Substances 0.000 claims 1
- 239000000463 material Substances 0.000 claims 1
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 claims 1
- 239000002245 particle Substances 0.000 claims 1
- 239000000243 solution Substances 0.000 claims 1
- 125000001424 substituent group Chemical group 0.000 claims 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims 1
- 229920002554 vinyl polymer Polymers 0.000 claims 1
- 235000019165 vitamin E Nutrition 0.000 claims 1
- 229940046009 vitamin E Drugs 0.000 claims 1
- 239000011709 vitamin E Substances 0.000 claims 1
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP13156549 | 2013-02-25 | ||
| EP13156549.1 | 2013-02-25 | ||
| PCT/US2014/017251 WO2014130603A1 (en) | 2013-02-25 | 2014-02-20 | Stabilized dental impression composition, kit of parts and use thereof |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| JP2016509057A JP2016509057A (ja) | 2016-03-24 |
| JP2016509057A5 true JP2016509057A5 (enExample) | 2017-03-23 |
| JP6341938B2 JP6341938B2 (ja) | 2018-06-13 |
Family
ID=47747504
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2015558933A Active JP6341938B2 (ja) | 2013-02-25 | 2014-02-20 | 安定化歯科用印象組成物、部品キット、及びそれらの使用 |
Country Status (4)
| Country | Link |
|---|---|
| US (1) | US9549881B2 (enExample) |
| EP (1) | EP2958538B1 (enExample) |
| JP (1) | JP6341938B2 (enExample) |
| WO (1) | WO2014130603A1 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11597830B2 (en) | 2017-06-20 | 2023-03-07 | 3M Innovative Properties Company | Radiation curable composition for additive manufacturing processes |
| KR102595989B1 (ko) * | 2018-10-02 | 2023-10-31 | 엘켐 실리콘즈 유에스에이 코포레이션 | 특히 의료 기기에서 사용하기 위한 맞춤 가능한 살 시뮬레이팅 실리콘 젤 또는 실리콘 발포체를 제조하기 위한 키트 |
| EP3824868B1 (en) * | 2019-11-20 | 2023-10-11 | Zhermack S.p.a. | Curable composition for dental impression |
| US20230165665A1 (en) * | 2020-04-08 | 2023-06-01 | Self-Ie Enterprise Private Limited | Dental alignment device and method |
| WO2023182518A1 (ja) * | 2022-03-25 | 2023-09-28 | 三井化学株式会社 | 重合促進剤、重合開始剤、硬化性組成物調製用キット、硬化性組成物、硬化物及び歯科材料 |
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| JP5123177B2 (ja) * | 2005-06-22 | 2013-01-16 | スリーエム イノベイティブ プロパティズ カンパニー | 改善された貯蔵特性を有する親水化された硬化性シリコーン印象材 |
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| EP2231102B1 (en) | 2007-12-18 | 2011-09-21 | 3M Innovative Properties Company | Dental composition containing a surfactant and an f-containing compound, process of production and use thereof |
| JP5332437B2 (ja) | 2008-09-18 | 2013-11-06 | 株式会社ジーシー | 歯科印象材用親水性オルガノポリシロキサン組成物 |
| DE102010028973A1 (de) | 2010-05-12 | 2011-11-17 | Voco Gmbh | Tenside enthaltende Zusammensetzung zur dentalen Abformung |
-
2014
- 2014-02-20 JP JP2015558933A patent/JP6341938B2/ja active Active
- 2014-02-20 WO PCT/US2014/017251 patent/WO2014130603A1/en not_active Ceased
- 2014-02-20 EP EP14708422.2A patent/EP2958538B1/en active Active
- 2014-02-20 US US14/767,167 patent/US9549881B2/en active Active
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