AU629432B2 - Process for the optical distinction of a dental material and dental material for said process - Google Patents
Process for the optical distinction of a dental material and dental material for said process Download PDFInfo
- Publication number
- AU629432B2 AU629432B2 AU67670/90A AU6767090A AU629432B2 AU 629432 B2 AU629432 B2 AU 629432B2 AU 67670/90 A AU67670/90 A AU 67670/90A AU 6767090 A AU6767090 A AU 6767090A AU 629432 B2 AU629432 B2 AU 629432B2
- Authority
- AU
- Australia
- Prior art keywords
- pyrano
- derivatives
- dione
- dental material
- dimethylamino
- 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.)
- Ceased
Links
- 239000005548 dental material Substances 0.000 title claims abstract description 50
- 238000000034 method Methods 0.000 title claims abstract description 27
- 230000003287 optical effect Effects 0.000 title claims abstract description 8
- 239000000463 material Substances 0.000 claims abstract description 21
- 239000000758 substrate Substances 0.000 claims abstract description 12
- 238000010521 absorption reaction Methods 0.000 claims abstract description 5
- 239000000126 substance Substances 0.000 claims description 24
- 238000011049 filling Methods 0.000 claims description 7
- 239000000203 mixture Substances 0.000 claims description 7
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims description 6
- 238000001914 filtration Methods 0.000 claims description 5
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical class C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims description 5
- 150000001251 acridines Chemical class 0.000 claims description 4
- 125000003914 fluoranthenyl group Chemical class C1(=CC=C2C=CC=C3C4=CC=CC=C4C1=C23)* 0.000 claims description 4
- GOLORTLGFDVFDW-UHFFFAOYSA-N 3-(1h-benzimidazol-2-yl)-7-(diethylamino)chromen-2-one Chemical compound C1=CC=C2NC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 GOLORTLGFDVFDW-UHFFFAOYSA-N 0.000 claims description 3
- KSEJNTBYAJRFMU-UHFFFAOYSA-N 5-(dimethylamino)-2-methylisoindole-1,3-dione Chemical compound CN(C)C1=CC=C2C(=O)N(C)C(=O)C2=C1 KSEJNTBYAJRFMU-UHFFFAOYSA-N 0.000 claims description 3
- KMEBUNSLFRQSEM-UHFFFAOYSA-N 5-amino-2-methylisoindole-1,3-dione Chemical compound C1=C(N)C=C2C(=O)N(C)C(=O)C2=C1 KMEBUNSLFRQSEM-UHFFFAOYSA-N 0.000 claims description 3
- 229940027998 antiseptic and disinfectant acridine derivative Drugs 0.000 claims description 3
- UWNADWZGEHDQAB-UHFFFAOYSA-N i-Pr2C2H4i-Pr2 Natural products CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 claims description 3
- OUQVKRKGTAUJQA-UHFFFAOYSA-N n-[(1-chloro-4-hydroxyisoquinolin-3-yl)carbonyl]glycine Chemical compound C1=CC=CC2=C(O)C(C(=O)NCC(=O)O)=NC(Cl)=C21 OUQVKRKGTAUJQA-UHFFFAOYSA-N 0.000 claims description 3
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-N 0.000 claims description 3
- 150000005075 thioxanthenes Chemical class 0.000 claims description 3
- 150000003732 xanthenes Chemical class 0.000 claims description 3
- PDKPRWFMRVBCOB-JLHYYAGUSA-N (e)-3-[4-(dimethylamino)phenyl]-1-phenylprop-2-en-1-one Chemical compound C1=CC(N(C)C)=CC=C1\C=C\C(=O)C1=CC=CC=C1 PDKPRWFMRVBCOB-JLHYYAGUSA-N 0.000 claims description 2
- SQPGRXNYOOVBIY-UHFFFAOYSA-N 1h-pyrano[2,3-h]quinoline-2,5-dione Chemical class C12=CC=COC2=CC(=O)C2=C1NC(=O)C=C2 SQPGRXNYOOVBIY-UHFFFAOYSA-N 0.000 claims description 2
- VAQYGOTYKYMSRX-UHFFFAOYSA-N 1h-pyrazole;quinoxaline Chemical class C=1C=NNC=1.N1=CC=NC2=CC=CC=C21 VAQYGOTYKYMSRX-UHFFFAOYSA-N 0.000 claims description 2
- BGQDCDRDPCVLJE-UHFFFAOYSA-N 3-methoxybenzo[b]phenalen-7-one Chemical compound C12=CC=CC=C2C(=O)C2=CC=CC3=C2C1=CC=C3OC BGQDCDRDPCVLJE-UHFFFAOYSA-N 0.000 claims description 2
- SYUWDSSYDVWBGD-UHFFFAOYSA-N 7-ethoxyacridine-3,9-diamine;hydrochloride Chemical compound Cl.C1=C(N)C=CC2=C(N)C3=CC(OCC)=CC=C3N=C21 SYUWDSSYDVWBGD-UHFFFAOYSA-N 0.000 claims description 2
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims description 2
- JLCDGIZDXAVSJD-UHFFFAOYSA-N C1C2=CC=CC=C2SC2=C1C1=CC=C(C(O)=NCCCCCCCCCCCCCCCCCC)C(C(O)=O)=C1C=C2 Chemical compound C1C2=CC=CC=C2SC2=C1C1=CC=C(C(O)=NCCCCCCCCCCCCCCCCCC)C(C(O)=O)=C1C=C2 JLCDGIZDXAVSJD-UHFFFAOYSA-N 0.000 claims description 2
- WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 claims description 2
- BGLGAKMTYHWWKW-UHFFFAOYSA-N acridine yellow Chemical compound [H+].[Cl-].CC1=C(N)C=C2N=C(C=C(C(C)=C3)N)C3=CC2=C1 BGLGAKMTYHWWKW-UHFFFAOYSA-N 0.000 claims description 2
- 239000003795 chemical substances by application Substances 0.000 claims description 2
- 150000004775 coumarins Chemical class 0.000 claims description 2
- DPVLADDAOKZJFL-UHFFFAOYSA-N ctk0h7318 Chemical compound C12=CC=CC=C2C2=CC=CC3=C2C1=CC1=C3C(=O)OC1=O DPVLADDAOKZJFL-UHFFFAOYSA-N 0.000 claims description 2
- QDLAGTHXVHQKRE-UHFFFAOYSA-N lichenxanthone Natural products COC1=CC(O)=C2C(=O)C3=C(C)C=C(OC)C=C3OC2=C1 QDLAGTHXVHQKRE-UHFFFAOYSA-N 0.000 claims description 2
- CSHWQDPOILHKBI-UHFFFAOYSA-N peryrene Natural products C1=CC(C2=CC=CC=3C2=C2C=CC=3)=C3C2=CC=CC3=C1 CSHWQDPOILHKBI-UHFFFAOYSA-N 0.000 claims description 2
- 159000000000 sodium salts Chemical class 0.000 claims description 2
- DPNRMEJBKMQHMC-UHFFFAOYSA-N tert-butyl 2-[6-(cyanomethyl)-2,2-dimethyl-1,3-dioxan-4-yl]acetate Chemical compound CC(C)(C)OC(=O)CC1CC(CC#N)OC(C)(C)O1 DPNRMEJBKMQHMC-UHFFFAOYSA-N 0.000 claims description 2
- 150000001875 compounds Chemical class 0.000 claims 11
- 125000002147 dimethylamino group Chemical group [H]C([H])([H])N(*)C([H])([H])[H] 0.000 claims 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 2
- VCLFGTPLJKNITL-UHFFFAOYSA-N 18-methyl-15-oxapentacyclo[10.6.1.02,7.08,19.013,17]nonadeca-1(18),2,4,6,8,10,12(19),13(17)-octaene-14,16-dione Chemical compound C12=CC=CC=C2C2=CC=CC3=C2C1=C(C)C1=C3C(=O)OC1=O VCLFGTPLJKNITL-UHFFFAOYSA-N 0.000 claims 1
- AZRRZGIBBLWSSQ-UHFFFAOYSA-N 4-ethyl-7-phenyl-3,5-diazabicyclo[2.2.2]octane-2,6-dione Chemical compound N1C(=O)C2C(=O)NC1(CC)CC2C1=CC=CC=C1 AZRRZGIBBLWSSQ-UHFFFAOYSA-N 0.000 claims 1
- KZFUMWVJJNDGAU-UHFFFAOYSA-N 7-(diethylamino)-3-(1-methylbenzimidazol-2-yl)chromen-2-one Chemical compound C1=CC=C2N(C)C(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 KZFUMWVJJNDGAU-UHFFFAOYSA-N 0.000 claims 1
- CFNMUZCFSDMZPQ-GHXNOFRVSA-N 7-[(z)-3-methyl-4-(4-methyl-5-oxo-2h-furan-2-yl)but-2-enoxy]chromen-2-one Chemical compound C=1C=C2C=CC(=O)OC2=CC=1OC/C=C(/C)CC1OC(=O)C(C)=C1 CFNMUZCFSDMZPQ-GHXNOFRVSA-N 0.000 claims 1
- PQJUJGAVDBINPI-UHFFFAOYSA-N 9H-thioxanthene Chemical compound C1=CC=C2CC3=CC=CC=C3SC2=C1 PQJUJGAVDBINPI-UHFFFAOYSA-N 0.000 claims 1
- XBDQKXXYIPTUBI-UHFFFAOYSA-N Propionic acid Chemical compound CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 claims 1
- 239000011797 cavity material Substances 0.000 claims 1
- VSSSHNJONFTXHS-UHFFFAOYSA-N coumarin 153 Chemical compound C12=C3CCCN2CCCC1=CC1=C3OC(=O)C=C1C(F)(F)F VSSSHNJONFTXHS-UHFFFAOYSA-N 0.000 claims 1
- WYVHNCGXVPMYQK-UHFFFAOYSA-N fluorol yellow 088 Chemical compound C1=CC=C2C(C=3C(=CC=C(C=3)C)O3)=C4C3=CC=C(C)C4=CC2=C1 WYVHNCGXVPMYQK-UHFFFAOYSA-N 0.000 claims 1
- BXYGQGOZARVRBW-UHFFFAOYSA-N n,n,3-trimethyl-1-phenylpyrazolo[4,3-b]quinoxalin-7-amine Chemical compound C12=NC3=CC(N(C)C)=CC=C3N=C2C(C)=NN1C1=CC=CC=C1 BXYGQGOZARVRBW-UHFFFAOYSA-N 0.000 claims 1
- XEPDKURZMUAWHZ-UHFFFAOYSA-N pyrano[2,3-f]chromene-2,5-dione Chemical class C12=CC=COC2=CC(=O)C2=C1OC(=O)C=C2 XEPDKURZMUAWHZ-UHFFFAOYSA-N 0.000 claims 1
- 239000002966 varnish Substances 0.000 description 15
- 238000006116 polymerization reaction Methods 0.000 description 9
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 8
- 239000002131 composite material Substances 0.000 description 8
- 230000000903 blocking effect Effects 0.000 description 7
- 239000003955 fissure sealant Substances 0.000 description 6
- 239000000178 monomer Substances 0.000 description 6
- 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 5
- OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 5
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 5
- 235000019400 benzoyl peroxide Nutrition 0.000 description 5
- KDTAEYOYAZPLIC-UHFFFAOYSA-N coumarin 152 Chemical compound FC(F)(F)C1=CC(=O)OC2=CC(N(C)C)=CC=C21 KDTAEYOYAZPLIC-UHFFFAOYSA-N 0.000 description 5
- 210000004268 dentin Anatomy 0.000 description 5
- 239000011253 protective coating Substances 0.000 description 5
- 239000000565 sealant Substances 0.000 description 5
- 125000006850 spacer group Chemical group 0.000 description 5
- 229920005372 Plexiglas® Polymers 0.000 description 4
- 239000003054 catalyst Substances 0.000 description 4
- 230000002452 interceptive effect Effects 0.000 description 4
- 150000002601 lanthanoid compounds Chemical class 0.000 description 4
- 239000003094 microcapsule Substances 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
- 229910002012 Aerosil® Inorganic materials 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 229930006711 bornane-2,3-dione Natural products 0.000 description 3
- 238000002156 mixing Methods 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 239000004926 polymethyl methacrylate Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- -1 1-methyl fluoranthene-2,3-dicarboxylic Chemical compound 0.000 description 2
- YIGGZEJDZIJLBX-UHFFFAOYSA-N 2,2-dihydroxyethyl 2-methylprop-2-enoate;1,6-diisocyanato-5,6-dimethylheptane Chemical compound CC(=C)C(=O)OCC(O)O.O=C=NC(C)(C)C(C)CCCCN=C=O YIGGZEJDZIJLBX-UHFFFAOYSA-N 0.000 description 2
- 229910002020 Aerosil® OX 50 Inorganic materials 0.000 description 2
- 229930185605 Bisphenol Natural products 0.000 description 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 229920004482 WACKER® Polymers 0.000 description 2
- 229940054058 antipsychotic thioxanthene derivative Drugs 0.000 description 2
- 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
- RWYFURDDADFSHT-RBBHPAOJSA-N diane Chemical class OC1=CC=C2[C@H]3CC[C@](C)([C@](CC4)(O)C#C)[C@@H]4[C@@H]3CCC2=C1.C1=C(Cl)C2=CC(=O)[C@@H]3CC3[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@@](C(C)=O)(OC(=O)C)[C@@]1(C)CC2 RWYFURDDADFSHT-RBBHPAOJSA-N 0.000 description 2
- 230000003760 hair shine Effects 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000004570 mortar (masonry) Substances 0.000 description 2
- FDPIMTJIUBPUKL-UHFFFAOYSA-N pentan-3-one Chemical compound CCC(=O)CC FDPIMTJIUBPUKL-UHFFFAOYSA-N 0.000 description 2
- 230000000704 physical effect Effects 0.000 description 2
- 230000001681 protective effect Effects 0.000 description 2
- XSCHRSMBECNVNS-UHFFFAOYSA-N quinoxaline Chemical compound N1=CC=NC2=CC=CC=C21 XSCHRSMBECNVNS-UHFFFAOYSA-N 0.000 description 2
- 229920002994 synthetic fiber Polymers 0.000 description 2
- KQMPMWGWJLNKPC-UHFFFAOYSA-N 1-(2-methylprop-2-enoyloxy)dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCC(OC(=O)C(C)=C)OC(=O)C(C)=C KQMPMWGWJLNKPC-UHFFFAOYSA-N 0.000 description 1
- JCDWHDCMMFCCTK-UHFFFAOYSA-N 1-phenylpyrazolo[4,3-b]quinoxaline Chemical compound C12=NC3=CC=CC=C3N=C2C=NN1C1=CC=CC=C1 JCDWHDCMMFCCTK-UHFFFAOYSA-N 0.000 description 1
- ITFWCGBCGYMQRP-UHFFFAOYSA-N 12h-benzo[a]thioxanthene-3,4-dicarboxylic acid Chemical compound C1C2=CC=CC=C2SC2=C1C1=CC=C(C(=O)O)C(C(O)=O)=C1C=C2 ITFWCGBCGYMQRP-UHFFFAOYSA-N 0.000 description 1
- KWVGIHKZDCUPEU-UHFFFAOYSA-N 2,2-dimethoxy-2-phenylacetophenone Chemical compound C=1C=CC=CC=1C(OC)(OC)C(=O)C1=CC=CC=C1 KWVGIHKZDCUPEU-UHFFFAOYSA-N 0.000 description 1
- RUBPVOQOOZQXET-UHFFFAOYSA-N 2-[[4-(dimethylamino)phenyl]iminomethyl]phenol Chemical compound C1=CC(N(C)C)=CC=C1N=CC1=CC=CC=C1O RUBPVOQOOZQXET-UHFFFAOYSA-N 0.000 description 1
- JUVSRZCUMWZBFK-UHFFFAOYSA-N 2-[n-(2-hydroxyethyl)-4-methylanilino]ethanol Chemical compound CC1=CC=C(N(CCO)CCO)C=C1 JUVSRZCUMWZBFK-UHFFFAOYSA-N 0.000 description 1
- NRZJOTSUPLCYDJ-UHFFFAOYSA-N 7-(ethylamino)-6-methyl-4-(trifluoromethyl)chromen-2-one Chemical compound O1C(=O)C=C(C(F)(F)F)C2=C1C=C(NCC)C(C)=C2 NRZJOTSUPLCYDJ-UHFFFAOYSA-N 0.000 description 1
- LCFVJGUPQDGYKZ-UHFFFAOYSA-N Bisphenol A diglycidyl ether Chemical compound C=1C=C(OCC2OC2)C=CC=1C(C)(C)C(C=C1)=CC=C1OCC1CO1 LCFVJGUPQDGYKZ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- AFCARXCZXQIEQB-UHFFFAOYSA-N N-[3-oxo-3-(2,4,6,7-tetrahydrotriazolo[4,5-c]pyridin-5-yl)propyl]-2-[[3-(trifluoromethoxy)phenyl]methylamino]pyrimidine-5-carboxamide Chemical compound O=C(CCNC(=O)C=1C=NC(=NC=1)NCC1=CC(=CC=C1)OC(F)(F)F)N1CC2=C(CC1)NN=N2 AFCARXCZXQIEQB-UHFFFAOYSA-N 0.000 description 1
- AFBPFSWMIHJQDM-UHFFFAOYSA-N N-methylaniline Chemical compound CNC1=CC=CC=C1 AFBPFSWMIHJQDM-UHFFFAOYSA-N 0.000 description 1
- INXWLSDYDXPENO-UHFFFAOYSA-N [2-(hydroxymethyl)-3-prop-2-enoyloxy-2-[[3-prop-2-enoyloxy-2,2-bis(prop-2-enoyloxymethyl)propoxy]methyl]propyl] prop-2-enoate Chemical compound C=CC(=O)OCC(COC(=O)C=C)(CO)COCC(COC(=O)C=C)(COC(=O)C=C)COC(=O)C=C INXWLSDYDXPENO-UHFFFAOYSA-N 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 230000002925 chemical effect Effects 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000003479 dental cement Substances 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000005284 excitation Effects 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 239000001034 iron oxide pigment Substances 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- NZBSAAMEZYOGBA-UHFFFAOYSA-N luminogren Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=CC3=CC=CC1=C23 NZBSAAMEZYOGBA-UHFFFAOYSA-N 0.000 description 1
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- HYXIJVZYRWWFOO-UHFFFAOYSA-N n,n,2,3-tetramethylaniline Chemical compound CN(C)C1=CC=CC(C)=C1C HYXIJVZYRWWFOO-UHFFFAOYSA-N 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- 239000004576 sand Substances 0.000 description 1
- IRFHMTUHTBSEBK-QGZVFWFLSA-N tert-butyl n-[(2s)-2-(2,5-difluorophenyl)-3-quinolin-3-ylpropyl]carbamate Chemical compound C1([C@H](CC=2C=C3C=CC=CC3=NC=2)CNC(=O)OC(C)(C)C)=CC(F)=CC=C1F IRFHMTUHTBSEBK-QGZVFWFLSA-N 0.000 description 1
- 238000012719 thermal polymerization Methods 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 238000009281 ultraviolet germicidal irradiation Methods 0.000 description 1
- 238000005406 washing Methods 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
- A61K6/60—Preparations for dentistry comprising organic or organo-metallic additives
- A61K6/65—Dyes
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K6/00—Preparations for dentistry
- A61K6/25—Compositions for detecting or measuring, e.g. of irregularities on natural or artificial teeth
-
- 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
- A61K6/887—Compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
Landscapes
- Health & Medical Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Biophysics (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Dental Preparations (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Dental Tools And Instruments Or Auxiliary Dental Instruments (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE3939998 | 1989-12-02 | ||
| DE3939998A DE3939998A1 (de) | 1989-12-02 | 1989-12-02 | Verfahren zur optischen unterscheidung eines dentalwerkstoffes sowie dentalwerkstoff dafuer |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU6767090A AU6767090A (en) | 1991-06-06 |
| AU629432B2 true AU629432B2 (en) | 1992-10-01 |
Family
ID=6394740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU67670/90A Ceased AU629432B2 (en) | 1989-12-02 | 1990-11-30 | Process for the optical distinction of a dental material and dental material for said process |
Country Status (6)
| Country | Link |
|---|---|
| US (1) | US5102461A (enExample) |
| EP (1) | EP0431452B1 (enExample) |
| AT (1) | ATE112483T1 (enExample) |
| AU (1) | AU629432B2 (enExample) |
| CA (1) | CA2031268C (enExample) |
| DE (2) | DE3939998A1 (enExample) |
Families Citing this family (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US5739170A (en) | 1992-09-11 | 1998-04-14 | The Regents Of The University Of California | Inhibitors of metazoan parasite proteases |
| DE19520016C2 (de) * | 1995-05-26 | 1997-04-30 | Ivoclar Ag | Photochrome Dentalmaterialien |
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| DE19719955C2 (de) | 1997-05-14 | 2000-09-14 | Deutsche Telekom Mobil | Verfahren zur Erreichbarkeit von Teilnehmern in einem Funkkommunikationssystem |
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| EP1634563B1 (en) * | 2004-09-07 | 2011-11-16 | S & C Polymer Silicon- und Composite-Spezialitäten GmbH | Dental polyalkenoate cement composition |
| EP1632211A1 (en) * | 2004-09-07 | 2006-03-08 | S & C Polymer Silicon- und Composite-Spezialitäten GmbH | Dental resin-modified polyalkenoate cement composition |
| US20060194895A1 (en) * | 2005-02-25 | 2006-08-31 | Dan Loveridge | Dental compositions having dual dental diagnostic capabilities and methods of use |
| US7314610B2 (en) * | 2005-02-25 | 2008-01-01 | Ultradent Products, Inc. | Dental compositions having anti-stokes up converters and methods of use |
| US20060194172A1 (en) * | 2005-02-25 | 2006-08-31 | Dan Loveridge | Dental compositions having a phosphorescent material and methods of use |
| WO2007025636A1 (en) | 2005-08-27 | 2007-03-08 | Universität Zürich | Illumination device for a dental handpiece, use thereof and method for selective removal of a tooth colored intra-coronal restoration |
| DE602006018175D1 (de) * | 2005-09-29 | 2010-12-23 | Dentsply Int Inc | Verfahren zur verwendung von dentalzusammensetzungen mit fluoreszierenden mitteln |
| US8263681B2 (en) * | 2006-12-28 | 2012-09-11 | 3M Innovative Properties Company | Dental compositions with natural tooth fluorescence |
| WO2008146875A1 (ja) * | 2007-05-31 | 2008-12-04 | Nihon University | 歯列矯正部材用接着材 |
| CN102245154B (zh) * | 2008-10-15 | 2014-09-03 | 3M创新有限公司 | 具有荧光颜料的牙科用组合物 |
| JP2010120864A (ja) * | 2008-11-17 | 2010-06-03 | Tokuyama Dental Corp | 齲蝕検知液 |
| FR3023163A1 (fr) * | 2014-07-07 | 2016-01-08 | Pharma G | Dispositif pour le scellement a usage dentaire, de protheses fixes et d'elements orthodontiques, contenant une molecule fluorescente a une concentration comprise entre 1% et 2,5% |
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| GB2190917A (en) * | 1986-05-26 | 1987-12-02 | G C Dental Ind Corp | Coating materials for protecting the surfaces of teeth |
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| DE1544923A1 (de) * | 1965-10-22 | 1969-10-09 | Bayer Ag | Verfahren zur Herstellung von kuenstlichen Zaehnen nach dem Pulver-Fluessigkeits-Verfahren |
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-
1989
- 1989-12-02 DE DE3939998A patent/DE3939998A1/de active Granted
-
1990
- 1990-11-28 DE DE59007387T patent/DE59007387D1/de not_active Expired - Fee Related
- 1990-11-28 EP EP90122703A patent/EP0431452B1/de not_active Expired - Lifetime
- 1990-11-28 AT AT90122703T patent/ATE112483T1/de not_active IP Right Cessation
- 1990-11-30 AU AU67670/90A patent/AU629432B2/en not_active Ceased
- 1990-11-30 US US07/620,470 patent/US5102461A/en not_active Expired - Lifetime
- 1990-11-30 CA CA002031268A patent/CA2031268C/en not_active Expired - Fee Related
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4600389A (en) * | 1984-10-29 | 1986-07-15 | Magnetic Activated Particle Sorting, Inc. | Dental restoration method and composition therefor |
| GB2190917A (en) * | 1986-05-26 | 1987-12-02 | G C Dental Ind Corp | Coating materials for protecting the surfaces of teeth |
Also Published As
| Publication number | Publication date |
|---|---|
| DE3939998C2 (enExample) | 1993-02-11 |
| DE59007387D1 (de) | 1994-11-10 |
| ATE112483T1 (de) | 1994-10-15 |
| CA2031268C (en) | 1995-04-18 |
| CA2031268A1 (en) | 1991-06-03 |
| EP0431452A2 (de) | 1991-06-12 |
| EP0431452A3 (en) | 1992-04-15 |
| US5102461A (en) | 1992-04-07 |
| DE3939998A1 (de) | 1991-06-06 |
| EP0431452B1 (de) | 1994-10-05 |
| AU6767090A (en) | 1991-06-06 |
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| Date | Code | Title | Description |
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| MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |