AU2005275242A1 - Dental compositions containing oxirane monomers - Google Patents
Dental compositions containing oxirane monomers Download PDFInfo
- Publication number
- AU2005275242A1 AU2005275242A1 AU2005275242A AU2005275242A AU2005275242A1 AU 2005275242 A1 AU2005275242 A1 AU 2005275242A1 AU 2005275242 A AU2005275242 A AU 2005275242A AU 2005275242 A AU2005275242 A AU 2005275242A AU 2005275242 A1 AU2005275242 A1 AU 2005275242A1
- Authority
- AU
- Australia
- Prior art keywords
- compound
- dental composition
- epoxy
- groups
- 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.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 94
- 239000000178 monomer Substances 0.000 title claims abstract description 41
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- 150000001875 compounds Chemical class 0.000 claims description 77
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- 125000003118 aryl group Chemical group 0.000 claims description 14
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- 125000001931 aliphatic group Chemical group 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 7
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- 125000002947 alkylene group Chemical group 0.000 claims description 6
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- 125000004432 carbon atom Chemical group C* 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
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- NHQDETIJWKXCTC-UHFFFAOYSA-N 3-chloroperbenzoic acid Chemical compound OOC(=O)C1=CC=CC(Cl)=C1 NHQDETIJWKXCTC-UHFFFAOYSA-N 0.000 description 5
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- 229940126062 Compound A Drugs 0.000 description 5
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- 239000007788 liquid Substances 0.000 description 5
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- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 description 5
- 239000010453 quartz Substances 0.000 description 5
- GTQHJCOHNAFHRE-UHFFFAOYSA-N 1,10-dibromodecane Chemical compound BrCCCCCCCCCCBr GTQHJCOHNAFHRE-UHFFFAOYSA-N 0.000 description 4
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- WCUXLLCKKVVCTQ-UHFFFAOYSA-M Potassium chloride Chemical compound [Cl-].[K+] WCUXLLCKKVVCTQ-UHFFFAOYSA-M 0.000 description 4
- 229960000583 acetic acid Drugs 0.000 description 4
- 230000015572 biosynthetic process Effects 0.000 description 4
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- DIOQZVSQGTUSAI-UHFFFAOYSA-N decane Chemical compound CCCCCCCCCC DIOQZVSQGTUSAI-UHFFFAOYSA-N 0.000 description 4
- GYZLOYUZLJXAJU-UHFFFAOYSA-N diglycidyl ether Chemical compound C1OC1COCC1CO1 GYZLOYUZLJXAJU-UHFFFAOYSA-N 0.000 description 4
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- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 4
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- 238000003786 synthesis reaction Methods 0.000 description 4
- 238000004448 titration Methods 0.000 description 4
- VNQXSTWCDUXYEZ-UHFFFAOYSA-N 1,7,7-trimethylbicyclo[2.2.1]heptane-2,3-dione Chemical compound C1CC2(C)C(=O)C(=O)C1C2(C)C VNQXSTWCDUXYEZ-UHFFFAOYSA-N 0.000 description 3
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
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- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
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- 229940125904 compound 1 Drugs 0.000 description 3
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- HLIAAMZDZWSSQW-UHFFFAOYSA-N 2-[[2-[3-[2-(oxiran-2-ylmethyl)phenoxy]propoxy]phenyl]methyl]oxirane Chemical compound C=1C=CC=C(CC2OC2)C=1OCCCOC1=CC=CC=C1CC1CO1 HLIAAMZDZWSSQW-UHFFFAOYSA-N 0.000 description 2
- QIRNGVVZBINFMX-UHFFFAOYSA-N 2-allylphenol Chemical compound OC1=CC=CC=C1CC=C QIRNGVVZBINFMX-UHFFFAOYSA-N 0.000 description 2
- FRIBMENBGGCKPD-UHFFFAOYSA-N 3-(2,3-dimethoxyphenyl)prop-2-enal Chemical compound COC1=CC=CC(C=CC=O)=C1OC FRIBMENBGGCKPD-UHFFFAOYSA-N 0.000 description 2
- 231100000148 Ames mutagenicity Toxicity 0.000 description 2
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- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
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- IISBACLAFKSPIT-UHFFFAOYSA-N bisphenol A Chemical compound C=1C=C(O)C=CC=1C(C)(C)C1=CC=C(O)C=C1 IISBACLAFKSPIT-UHFFFAOYSA-N 0.000 description 2
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- 125000005397 methacrylic acid ester group Chemical group 0.000 description 2
- 239000012044 organic layer Substances 0.000 description 2
- 125000000466 oxiranyl group Chemical group 0.000 description 2
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 description 2
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- YBMGCAUHJDRHAS-UHFFFAOYSA-N 2-[[2-[1-[2-(oxiran-2-ylmethyl)phenoxy]hexan-3-yloxy]phenyl]methyl]oxirane Chemical compound C=1C=CC=C(CC2OC2)C=1OC(CCC)CCOC1=CC=CC=C1CC1CO1 YBMGCAUHJDRHAS-UHFFFAOYSA-N 0.000 description 1
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- CMYKHUZEKJXFAD-UHFFFAOYSA-N 2-[[2-[5-[2-(oxiran-2-ylmethyl)phenoxy]pentoxy]phenyl]methyl]oxirane Chemical compound C=1C=CC=C(CC2OC2)C=1OCCCCCOC1=CC=CC=C1CC1CO1 CMYKHUZEKJXFAD-UHFFFAOYSA-N 0.000 description 1
- NZNGWCSOENLSCX-UHFFFAOYSA-N 2-[[2-[6-[2-(oxiran-2-ylmethyl)phenoxy]hexoxy]phenyl]methyl]oxirane Chemical compound C=1C=CC=C(CC2OC2)C=1OCCCCCCOC1=CC=CC=C1CC1CO1 NZNGWCSOENLSCX-UHFFFAOYSA-N 0.000 description 1
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- VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- FYYIUODUDSPAJQ-XVBQNVSMSA-N [(1S,6R)-7-oxabicyclo[4.1.0]heptan-3-yl]methyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC1CC[C@H]2O[C@H]2C1 FYYIUODUDSPAJQ-XVBQNVSMSA-N 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 238000012644 addition polymerization Methods 0.000 description 1
- 150000001336 alkenes Chemical group 0.000 description 1
- 230000004075 alteration Effects 0.000 description 1
- 235000012211 aluminium silicate Nutrition 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 238000004458 analytical method Methods 0.000 description 1
- 229910052787 antimony Inorganic materials 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 150000001491 aromatic compounds Chemical class 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910052788 barium Inorganic materials 0.000 description 1
- WURBFLDFSFBTLW-UHFFFAOYSA-N benzil Chemical compound C=1C=CC=CC=1C(=O)C(=O)C1=CC=CC=C1 WURBFLDFSFBTLW-UHFFFAOYSA-N 0.000 description 1
- 230000002902 bimodal effect Effects 0.000 description 1
- 230000008033 biological extinction Effects 0.000 description 1
- LMMDJMWIHPEQSJ-UHFFFAOYSA-N bis[(3-methyl-7-oxabicyclo[4.1.0]heptan-4-yl)methyl] hexanedioate Chemical compound C1C2OC2CC(C)C1COC(=O)CCCCC(=O)OCC1CC2OC2CC1C LMMDJMWIHPEQSJ-UHFFFAOYSA-N 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 150000001642 boronic acid derivatives Chemical class 0.000 description 1
- 239000005388 borosilicate glass Substances 0.000 description 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
- 238000012656 cationic ring opening polymerization Methods 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 239000007795 chemical reaction product Substances 0.000 description 1
- XENVCRGQTABGKY-ZHACJKMWSA-N chlorohydrin Chemical compound CC#CC#CC#CC#C\C=C\C(Cl)CO XENVCRGQTABGKY-ZHACJKMWSA-N 0.000 description 1
- 239000008119 colloidal silica Substances 0.000 description 1
- 238000004440 column chromatography Methods 0.000 description 1
- 239000008139 complexing agent Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 239000007822 coupling agent Substances 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- ZWAJLVLEBYIOTI-UHFFFAOYSA-N cyclohexene oxide Chemical group C1CCCC2OC21 ZWAJLVLEBYIOTI-UHFFFAOYSA-N 0.000 description 1
- 239000008367 deionised water Substances 0.000 description 1
- 229910021641 deionized water Inorganic materials 0.000 description 1
- 239000012933 diacyl peroxide Substances 0.000 description 1
- 239000010432 diamond Substances 0.000 description 1
- 229910003460 diamond Inorganic materials 0.000 description 1
- OZLBDYMWFAHSOQ-UHFFFAOYSA-N diphenyliodanium Chemical compound C=1C=CC=CC=1[I+]C1=CC=CC=C1 OZLBDYMWFAHSOQ-UHFFFAOYSA-N 0.000 description 1
- RSJLWBUYLGJOBD-UHFFFAOYSA-M diphenyliodanium;chloride Chemical compound [Cl-].C=1C=CC=CC=1[I+]C1=CC=CC=C1 RSJLWBUYLGJOBD-UHFFFAOYSA-M 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 125000004185 ester group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000010433 feldspar Substances 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000011049 filling Methods 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 238000002290 gas chromatography-mass spectrometry Methods 0.000 description 1
- VOZRXNHHFUQHIL-UHFFFAOYSA-N glycidyl methacrylate Chemical compound CC(=C)C(=O)OCC1CO1 VOZRXNHHFUQHIL-UHFFFAOYSA-N 0.000 description 1
- 230000020169 heat generation Effects 0.000 description 1
- 125000000623 heterocyclic group Chemical group 0.000 description 1
- 229920006158 high molecular weight polymer Polymers 0.000 description 1
- 239000001257 hydrogen Substances 0.000 description 1
- 229910052739 hydrogen Inorganic materials 0.000 description 1
- 150000002432 hydroperoxides Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- QWPPOHNGKGFGJK-UHFFFAOYSA-N hypochlorous acid Chemical compound ClO QWPPOHNGKGFGJK-UHFFFAOYSA-N 0.000 description 1
- 230000001939 inductive effect Effects 0.000 description 1
- 229920000554 ionomer Polymers 0.000 description 1
- NLYAJNPCOHFWQQ-UHFFFAOYSA-N kaolin Chemical compound O.O.O=[Al]O[Si](=O)O[Si](=O)O[Al]=O NLYAJNPCOHFWQQ-UHFFFAOYSA-N 0.000 description 1
- 239000010410 layer Substances 0.000 description 1
- 230000031700 light absorption Effects 0.000 description 1
- 229910044991 metal oxide Inorganic materials 0.000 description 1
- 150000004706 metal oxides Chemical class 0.000 description 1
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical class CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 description 1
- WJLXMNAAJLNWAB-UHFFFAOYSA-N methyl-bis[2-(7-oxabicyclo[4.1.0]heptan-4-yl)ethyl]-phenylsilane Chemical compound C1CC2OC2CC1CC[Si](C)(CCC1CC2OC2CC1)C1=CC=CC=C1 WJLXMNAAJLNWAB-UHFFFAOYSA-N 0.000 description 1
- 239000011859 microparticle Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002105 nanoparticle Substances 0.000 description 1
- 150000004767 nitrides Chemical class 0.000 description 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 239000012766 organic filler Substances 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 150000002921 oxetanes Chemical class 0.000 description 1
- 150000002924 oxiranes Chemical class 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229960003540 oxyquinoline Drugs 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000002976 peresters Chemical class 0.000 description 1
- 125000000864 peroxy group Chemical group O(O*)* 0.000 description 1
- 150000002989 phenols 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
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002857 polybutadiene Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 229920000909 polytetrahydrofuran Polymers 0.000 description 1
- 230000008569 process Effects 0.000 description 1
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 238000011160 research Methods 0.000 description 1
- 239000013557 residual solvent Substances 0.000 description 1
- 238000007142 ring opening reaction Methods 0.000 description 1
- 238000005096 rolling process Methods 0.000 description 1
- 239000002631 root canal filling material Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000012488 sample solution Substances 0.000 description 1
- 239000000565 sealant Substances 0.000 description 1
- 238000010008 shearing Methods 0.000 description 1
- 229910000077 silane Inorganic materials 0.000 description 1
- HQVNEWCFYHHQES-UHFFFAOYSA-N silicon nitride Chemical compound N12[Si]34N5[Si]62N3[Si]51N64 HQVNEWCFYHHQES-UHFFFAOYSA-N 0.000 description 1
- 229920002379 silicone rubber Polymers 0.000 description 1
- 239000004945 silicone rubber Substances 0.000 description 1
- 125000005373 siloxane group Chemical group [SiH2](O*)* 0.000 description 1
- 239000001632 sodium acetate Substances 0.000 description 1
- 235000017281 sodium acetate Nutrition 0.000 description 1
- JVBXVOWTABLYPX-UHFFFAOYSA-L sodium dithionite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])=O JVBXVOWTABLYPX-UHFFFAOYSA-L 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 238000004611 spectroscopical analysis Methods 0.000 description 1
- 238000010183 spectrum analysis Methods 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 238000004381 surface treatment Methods 0.000 description 1
- 229920002994 synthetic fiber Polymers 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- JRMUNVKIHCOMHV-UHFFFAOYSA-M tetrabutylammonium bromide Chemical compound [Br-].CCCC[N+](CCCC)(CCCC)CCCC JRMUNVKIHCOMHV-UHFFFAOYSA-M 0.000 description 1
- 238000004809 thin layer chromatography Methods 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011043 treated quartz Substances 0.000 description 1
- 229940045860 white wax Drugs 0.000 description 1
- RBORBHYCVONNJH-UHFFFAOYSA-K yttrium(iii) fluoride Chemical compound F[Y](F)F RBORBHYCVONNJH-UHFFFAOYSA-K 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052726 zirconium Inorganic materials 0.000 description 1
- SXPUVBFQXJHYNS-UHFFFAOYSA-N α-furil Chemical compound C=1C=COC=1C(=O)C(=O)C1=CC=CO1 SXPUVBFQXJHYNS-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/50—Preparations specially adapted for dental root treatment
- A61K6/54—Filling; Sealing
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/20—Protective coatings for natural or artificial teeth, e.g. sealings, dye coatings or varnish
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/30—Compositions for temporarily or permanently fixing teeth or palates, e.g. primers for dental adhesives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/80—Preparations for artificial teeth, for filling teeth or for capping teeth
- A61K6/884—Preparations for artificial teeth, for filling teeth or for capping teeth comprising natural or synthetic resins
- A61K6/891—Compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Dental Preparations (AREA)
- Epoxy Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US58797704P | 2004-07-14 | 2004-07-14 | |
| US60/587,977 | 2004-07-14 | ||
| PCT/US2005/024822 WO2006019797A1 (en) | 2004-07-14 | 2005-07-13 | Dental compositions containing oxirane monomers |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AU2005275242A1 true AU2005275242A1 (en) | 2006-02-23 |
Family
ID=35115863
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU2005275242A Abandoned AU2005275242A1 (en) | 2004-07-14 | 2005-07-13 | Dental compositions containing oxirane monomers |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US20080085494A1 (enExample) |
| EP (1) | EP1781238B1 (enExample) |
| JP (1) | JP4827145B2 (enExample) |
| CN (1) | CN100569209C (enExample) |
| AT (1) | ATE425734T1 (enExample) |
| AU (1) | AU2005275242A1 (enExample) |
| CA (1) | CA2573244A1 (enExample) |
| DE (1) | DE602005013389D1 (enExample) |
| WO (1) | WO2006019797A1 (enExample) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5153635B2 (ja) * | 2006-08-15 | 2013-02-27 | 昭和電工株式会社 | 新規エポキシ化合物およびその製造方法 |
| JP2009179568A (ja) * | 2008-01-29 | 2009-08-13 | Nippon Shokubai Co Ltd | 芳香族骨格含有脂環式エポキシ化合物、その製造方法、芳香族骨格含有脂環式エポキシ樹脂組成物並びにその成形体及び光学部材 |
| CN102665605B (zh) | 2009-12-22 | 2016-06-01 | 3M创新有限公司 | 牙科用组合物、铣削块和方法 |
| WO2015051196A1 (en) * | 2013-10-02 | 2015-04-09 | The Board Of Regents Of The University Of Texas System | Improving color and release profile of resin compositions comprising silver nanoparticles |
| FR3035106A1 (fr) * | 2015-04-17 | 2016-10-21 | Centre De Coop Int En Rech Agronomique Pour Le Dev (Cirad) | Dimere polyaromatique glycidyle |
| CN107849223B (zh) | 2015-07-10 | 2020-07-28 | 住友精化株式会社 | 环氧树脂组合物、其制造方法、以及该组合物的用途 |
| KR102459583B1 (ko) | 2017-01-10 | 2022-10-28 | 스미토모 세이카 가부시키가이샤 | 에폭시 수지 조성물 |
| CN110177819B (zh) | 2017-01-10 | 2022-11-08 | 住友精化株式会社 | 环氧树脂组合物 |
| EP3569626B1 (en) | 2017-01-10 | 2023-03-01 | Sumitomo Seika Chemicals Co., Ltd. | Epoxy resin composition |
| CN110191921B (zh) * | 2017-01-10 | 2022-04-26 | 住友精化株式会社 | 环氧树脂组合物 |
| TW201910376A (zh) * | 2017-07-31 | 2019-03-16 | 日商住友精化股份有限公司 | 環氧樹脂組成物 |
Family Cites Families (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| NL105599C (enExample) * | 1956-04-12 | |||
| US3018262A (en) * | 1957-05-01 | 1962-01-23 | Shell Oil Co | Curing polyepoxides with certain metal salts of inorganic acids |
| US3971754A (en) * | 1973-12-10 | 1976-07-27 | Pennwalt Corporation | X-ray opaque, enamel-matching dental filling composition |
| US4695251A (en) * | 1980-04-07 | 1987-09-22 | Minnesota Mining And Manufacturing Company | Orthodontic bracket adhesive and abrasive for removal thereof |
| US4391590A (en) * | 1981-04-09 | 1983-07-05 | Dentsply Research & Development Corp. | Cartridge for viscous material |
| US4503169A (en) * | 1984-04-19 | 1985-03-05 | Minnesota Mining And Manufacturing Company | Radiopaque, low visual opacity dental composites containing non-vitreous microparticles |
| DE3609038A1 (de) * | 1986-03-18 | 1987-09-24 | Espe Stiftung | Roentgenopake polymerisierbare dentalmassen |
| US4788268A (en) * | 1987-05-05 | 1988-11-29 | Hughes Aircraft Company | Method for preparation of epoxysilicone compounds and allyl-terminated silicone compounds |
| US5037861A (en) * | 1989-08-09 | 1991-08-06 | General Electric Company | Novel highly reactive silicon-containing epoxides |
| US5165890A (en) * | 1991-01-07 | 1992-11-24 | Centrix, Inc. | Dosing dental cartridge |
| US6699946B1 (en) * | 1991-12-13 | 2004-03-02 | Solvay (Societe Anonyme) | Polyphenylene sulphide-based compositions with improved impact strength and process for preparing them |
| US5322440A (en) * | 1992-10-20 | 1994-06-21 | Kerr Manufacturing Company | Dental syringe tip |
| US5856373A (en) * | 1994-10-31 | 1999-01-05 | Minnesota Mining And Manufacturing Company | Dental visible light curable epoxy system with enhanced depth of cure |
| US5770706A (en) * | 1995-06-07 | 1998-06-23 | National Starch And Chemical Investment Holding Corporation | Snap-cure epoxy adhesives |
| DE19648283A1 (de) * | 1996-11-21 | 1998-05-28 | Thera Ges Fuer Patente | Polymerisierbare Massen auf der Basis von Epoxiden |
| US5998495A (en) * | 1997-04-11 | 1999-12-07 | 3M Innovative Properties Company | Ternary photoinitiator system for curing of epoxy/polyol resin compositions |
| US6506816B1 (en) * | 1997-07-17 | 2003-01-14 | 3M Innovative Properties Company | Dental resin cements having improved handling properties |
| DE19736471A1 (de) * | 1997-08-21 | 1999-02-25 | Espe Dental Ag | Lichtinduziert kationisch härtende Zusammensetzungen und deren Verwendung |
| US6187836B1 (en) * | 1998-06-05 | 2001-02-13 | 3M Innovative Properties Company | Compositions featuring cationically active and free radically active functional groups, and methods for polymerizing such compositions |
| FR2784025B1 (fr) * | 1998-10-02 | 2002-10-31 | Rhodia Chimie Sa | Composition dentaire a base d'une silicone fonctionnalisee reticulable/polymerisable par voie cationique |
| US6306926B1 (en) * | 1998-10-07 | 2001-10-23 | 3M Innovative Properties Company | Radiopaque cationically polymerizable compositions comprising a radiopacifying filler, and method for polymerizing same |
| US6572693B1 (en) * | 1999-10-28 | 2003-06-03 | 3M Innovative Properties Company | Aesthetic dental materials |
| US6387981B1 (en) * | 1999-10-28 | 2002-05-14 | 3M Innovative Properties Company | Radiopaque dental materials with nano-sized particles |
| DE10001228B4 (de) * | 2000-01-13 | 2007-01-04 | 3M Espe Ag | Polymerisierbare Zubereitungen auf der Basis von siliziumhaltigen Epoxiden |
| US6670474B2 (en) * | 2001-04-17 | 2003-12-30 | R. Garth Pews | Epoxide derivatives of allylarylphenols |
| US6765036B2 (en) * | 2002-01-15 | 2004-07-20 | 3M Innovative Properties Company | Ternary photoinitiator system for cationically polymerizable resins |
| US6784248B2 (en) * | 2002-02-15 | 2004-08-31 | Ppg Industries Ohio, Inc. | Thermosetting compositions containing alternating copolymers of isobutylene type monomers |
| US7141684B2 (en) * | 2003-10-24 | 2006-11-28 | Pews R Garth | Diepoxide derivatives of diallyl phenolics |
| US7262228B2 (en) * | 2003-11-21 | 2007-08-28 | Curators Of The University Of Missouri | Photoinitiator systems with anthracene-based electron donors for curing cationically polymerizable resins |
| US7090721B2 (en) * | 2004-05-17 | 2006-08-15 | 3M Innovative Properties Company | Use of nanoparticles to adjust refractive index of dental compositions |
| US7156911B2 (en) * | 2004-05-17 | 2007-01-02 | 3M Innovative Properties Company | Dental compositions containing nanofillers and related methods |
| US7649029B2 (en) * | 2004-05-17 | 2010-01-19 | 3M Innovative Properties Company | Dental compositions containing nanozirconia fillers |
| CN101018536A (zh) * | 2004-07-14 | 2007-08-15 | 3M埃斯佩股份公司 | 含环氧官能可聚合化合物的牙科组合物 |
-
2005
- 2005-07-13 US US11/571,943 patent/US20080085494A1/en not_active Abandoned
- 2005-07-13 EP EP05770137A patent/EP1781238B1/en not_active Expired - Lifetime
- 2005-07-13 AT AT05770137T patent/ATE425734T1/de not_active IP Right Cessation
- 2005-07-13 DE DE602005013389T patent/DE602005013389D1/de not_active Expired - Lifetime
- 2005-07-13 WO PCT/US2005/024822 patent/WO2006019797A1/en not_active Ceased
- 2005-07-13 CA CA002573244A patent/CA2573244A1/en not_active Abandoned
- 2005-07-13 CN CNB2005800234183A patent/CN100569209C/zh not_active Expired - Fee Related
- 2005-07-13 AU AU2005275242A patent/AU2005275242A1/en not_active Abandoned
- 2005-07-13 JP JP2007521601A patent/JP4827145B2/ja not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| CN1997332A (zh) | 2007-07-11 |
| CA2573244A1 (en) | 2006-02-23 |
| JP2008506697A (ja) | 2008-03-06 |
| EP1781238B1 (en) | 2009-03-18 |
| WO2006019797A1 (en) | 2006-02-23 |
| JP4827145B2 (ja) | 2011-11-30 |
| DE602005013389D1 (de) | 2009-04-30 |
| ATE425734T1 (de) | 2009-04-15 |
| US20080085494A1 (en) | 2008-04-10 |
| CN100569209C (zh) | 2009-12-16 |
| EP1781238A1 (en) | 2007-05-09 |
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