CA2031268C - 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 processInfo
- Publication number
- CA2031268C CA2031268C CA002031268A CA2031268A CA2031268C CA 2031268 C CA2031268 C CA 2031268C CA 002031268 A CA002031268 A CA 002031268A CA 2031268 A CA2031268 A CA 2031268A CA 2031268 C CA2031268 C CA 2031268C
- Authority
- CA
- Canada
- Prior art keywords
- derivatives
- pyrano
- dione
- derivative
- 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.)
- Expired - Fee Related
Links
- 239000005548 dental material Substances 0.000 title claims abstract description 45
- 238000000034 method Methods 0.000 title claims abstract description 22
- 230000003287 optical effect Effects 0.000 title claims abstract description 7
- 239000000126 substance Substances 0.000 claims abstract description 25
- 239000000758 substrate Substances 0.000 claims abstract description 10
- 239000000203 mixture Substances 0.000 claims abstract description 8
- 125000002080 perylenyl group Chemical group C1(=CC=C2C=CC=C3C4=CC=CC5=CC=CC(C1=C23)=C45)* 0.000 claims abstract description 7
- VAQYGOTYKYMSRX-UHFFFAOYSA-N 1h-pyrazole;quinoxaline Chemical class C=1C=NNC=1.N1=CC=NC2=CC=CC=C21 VAQYGOTYKYMSRX-UHFFFAOYSA-N 0.000 claims abstract description 5
- 125000003914 fluoranthenyl group Chemical class C1(=CC=C2C=CC=C3C4=CC=CC=C4C1=C23)* 0.000 claims abstract description 5
- XKJCHHZQLQNZHY-UHFFFAOYSA-N phthalimide Chemical class C1=CC=C2C(=O)NC(=O)C2=C1 XKJCHHZQLQNZHY-UHFFFAOYSA-N 0.000 claims abstract description 5
- 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 abstract description 5
- 150000005075 thioxanthenes Chemical class 0.000 claims abstract description 5
- 125000001834 xanthenyl group Chemical class C1=CC=CC=2OC3=CC=CC=C3C(C12)* 0.000 claims abstract description 5
- 238000010521 absorption reaction Methods 0.000 claims abstract description 4
- 229940054058 antipsychotic thioxanthene derivative Drugs 0.000 claims abstract description 4
- 229940027998 antiseptic and disinfectant acridine derivative Drugs 0.000 claims abstract description 4
- 238000001914 filtration Methods 0.000 claims abstract description 4
- 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 claims description 7
- 150000001251 acridines Chemical class 0.000 claims description 4
- 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 3
- 150000004775 coumarins Chemical class 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
- 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
- SYRBOMODLUADBZ-RNIAWFEPSA-N 1-[(E)-[(E)-(2-hydroxynaphthalen-1-yl)methylidenehydrazinylidene]methyl]naphthalen-2-ol Chemical compound N(\N=C\C1=C(C=CC2=CC=CC=C12)O)=C/C1=C(C=CC2=CC=CC=C12)O SYRBOMODLUADBZ-RNIAWFEPSA-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
- 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 claims description 2
- 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 2
- YZACNHJLNWJNRH-UHFFFAOYSA-N 3-ethyl-n,n-dimethyl-1-phenylpyrazolo[4,3-b]quinoxalin-7-amine Chemical compound C12=NC3=CC(N(C)C)=CC=C3N=C2C(CC)=NN1C1=CC=CC=C1 YZACNHJLNWJNRH-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
- 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 2
- 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 2
- 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 description 2
- 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 claims description 2
- JBNOVHJXQSHGRL-UHFFFAOYSA-N 7-amino-4-(trifluoromethyl)coumarin Chemical compound FC(F)(F)C1=CC(=O)OC2=CC(N)=CC=C21 JBNOVHJXQSHGRL-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
- 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
- VBVAVBCYMYWNOU-UHFFFAOYSA-N coumarin 6 Chemical compound C1=CC=C2SC(C3=CC4=CC=C(C=C4OC3=O)N(CC)CC)=NC2=C1 VBVAVBCYMYWNOU-UHFFFAOYSA-N 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
- 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 description 2
- NISZMWZPLJGKCC-UHFFFAOYSA-N lissamine flavine FF free acid Chemical compound C1=CC(C)=CC=C1N(C1=O)C(=O)C2=C3C1=CC=CC3=C(N)C(S(O)(=O)=O)=C2 NISZMWZPLJGKCC-UHFFFAOYSA-N 0.000 claims description 2
- NZBSAAMEZYOGBA-UHFFFAOYSA-N luminogren Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=CC3=CC=CC1=C23 NZBSAAMEZYOGBA-UHFFFAOYSA-N 0.000 claims description 2
- 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 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
- 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
- KYRJCQVWCHDCSP-UHFFFAOYSA-N 3h-chromene-2,5-dione Chemical compound O=C1C=CC=C2OC(=O)CC=C21 KYRJCQVWCHDCSP-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
- VSSSHNJONFTXHS-UHFFFAOYSA-N coumarin 153 Chemical compound C12=C3CCCN2CCCC1=CC1=C3OC(=O)C=C1C(F)(F)F VSSSHNJONFTXHS-UHFFFAOYSA-N 0.000 claims 1
- JBPCDMSEJVCNGV-UHFFFAOYSA-N coumarin 334 Chemical compound C1CCC2=C(OC(C(C(=O)C)=C3)=O)C3=CC3=C2N1CCC3 JBPCDMSEJVCNGV-UHFFFAOYSA-N 0.000 claims 1
- LGDDFMCJIHJNMK-UHFFFAOYSA-N coumarin 337 Chemical compound C12=C3CCCN2CCCC1=CC1=C3OC(=O)C(C#N)=C1 LGDDFMCJIHJNMK-UHFFFAOYSA-N 0.000 claims 1
- KCDCNGXPPGQERR-UHFFFAOYSA-N coumarin 343 Chemical compound C1CCC2=C(OC(C(C(=O)O)=C3)=O)C3=CC3=C2N1CCC3 KCDCNGXPPGQERR-UHFFFAOYSA-N 0.000 claims 1
- 125000000641 acridinyl group Chemical class C1(=CC=CC2=NC3=CC=CC=C3C=C12)* 0.000 abstract 1
- 150000001893 coumarin derivatives Chemical class 0.000 abstract 1
- 239000000463 material Substances 0.000 description 17
- 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
- 238000011049 filling Methods 0.000 description 6
- 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
- 229910002012 Aerosil® Inorganic materials 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
- 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
- 150000002601 lanthanoid compounds Chemical class 0.000 description 4
- 239000003094 microcapsule Substances 0.000 description 4
- 239000004926 polymethyl methacrylate 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
- 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 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
- 230000002452 interceptive effect Effects 0.000 description 3
- 239000000049 pigment Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- 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 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-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
- 230000002925 chemical effect Effects 0.000 description 2
- 230000000694 effects Effects 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
- 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
- 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
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- AMFGWXWBFGVCKG-UHFFFAOYSA-N Panavia opaque Chemical compound C1=CC(OCC(O)COC(=O)C(=C)C)=CC=C1C(C)(C)C1=CC=C(OCC(O)COC(=O)C(C)=C)C=C1 AMFGWXWBFGVCKG-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
- 150000007942 carboxylates Chemical class 0.000 description 1
- 239000000919 ceramic Substances 0.000 description 1
- 238000002144 chemical decomposition reaction Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 239000003479 dental cement Substances 0.000 description 1
- -1 diisobutyl carboxylate Chemical class 0.000 description 1
- 238000002845 discoloration Methods 0.000 description 1
- 239000000975 dye Substances 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
- QSHDDOUJBYECFT-UHFFFAOYSA-N mercury Chemical compound [Hg] QSHDDOUJBYECFT-UHFFFAOYSA-N 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 230000002028 premature Effects 0.000 description 1
- LISFMEBWQUVKPJ-UHFFFAOYSA-N quinolin-2-ol Chemical compound C1=CC=C2NC(=O)C=CC2=C1 LISFMEBWQUVKPJ-UHFFFAOYSA-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
- 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 |
|---|---|---|---|
| DEP3939998.2 | 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 |
|---|---|
| CA2031268A1 CA2031268A1 (en) | 1991-06-03 |
| CA2031268C true CA2031268C (en) | 1995-04-18 |
Family
ID=6394740
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002031268A Expired - Fee Related CA2031268C (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 |
| US5667840A (en) * | 1996-02-27 | 1997-09-16 | Becton Dickinson And Company | Lubricant soluble fluorescent agent and method for its use in a system for detection of lubricant coatings |
| DE19719955C2 (de) | 1997-05-14 | 2000-09-14 | Deutsche Telekom Mobil | Verfahren zur Erreichbarkeit von Teilnehmern in einem Funkkommunikationssystem |
| DE19926728B4 (de) | 1999-06-11 | 2011-08-18 | 3M Espe Ag, 82229 | Verwendung von Trägermaterialien und diagnostisch nutzbaren Zusatzstoffen in Abbildungsverfahren für intraorale Diagnosezwecke |
| US7114951B2 (en) | 1999-11-10 | 2006-10-03 | Dentsply International Inc. | Method and shaped product-formed from low tack and fluorescing polymerizable dental material |
| US6391281B1 (en) | 2000-05-18 | 2002-05-21 | Medical College Of Georgia Research Institute | Fluorescent agent for the identification of tooth dentin |
| DE10061195B4 (de) | 2000-12-08 | 2004-12-02 | 3M Espe Ag | Verwendung von Abformmassen zur Herstellung von Behandlungsvorrichtungen |
| DE10106372A1 (de) * | 2001-02-12 | 2002-08-29 | Ivoclar Vivadent Ag | Thermochromer Dentalwerkstoff |
| DE10146883B4 (de) * | 2001-09-24 | 2006-05-24 | Dentona Ag | Mineralischer Rohstoff zur Herstellung dentaler Gipsmodelle mit fluoreszierender Oberfläche |
| 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% |
| EP3513778B1 (de) | 2018-01-23 | 2020-03-11 | Ivoclar Vivadent AG | Photochromer dentalwerkstoff mit verkapselten photochromen farbmittel |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3309274A (en) * | 1962-07-23 | 1967-03-14 | Brilliant Herbert | Use of fluorescent dyes in dental diagnostic methods |
| US3255079A (en) * | 1963-06-17 | 1966-06-07 | American Cyanamid Co | Therapeutic dental cement and a method for treating carious teeth |
| GB1068587A (en) * | 1963-12-06 | 1967-05-10 | Biorex Laboratories Ltd | Dental fillers and bone cements comprising collagen |
| DE1544923A1 (de) * | 1965-10-22 | 1969-10-09 | Bayer Ag | Verfahren zur Herstellung von kuenstlichen Zaehnen nach dem Pulver-Fluessigkeits-Verfahren |
| US3711700A (en) * | 1971-05-10 | 1973-01-16 | Gte Sylvania Inc | Disclosing light |
| GB1428672A (en) * | 1972-04-25 | 1976-03-17 | Amalgamated Dental Co Ltd | Polymerizable compositions suitable for dental use |
| US3960753A (en) * | 1974-05-30 | 1976-06-01 | Rca Corporation | Fluorescent liquid crystals |
| US4600389A (en) * | 1984-10-29 | 1986-07-15 | Magnetic Activated Particle Sorting, Inc. | Dental restoration method and composition therefor |
| US4977511A (en) * | 1985-11-20 | 1990-12-11 | The Mead Corporation | Photosensitive materials containing ionic dye compound as initiators |
| CH665483A5 (de) * | 1985-11-22 | 1988-05-13 | Coltene Ag | Verfahren zur kontrolle des homogenen durchmischens einer haertbaren masse und eine haertbare masse zur durchfuehrung des verfahrens. |
| JPS62277953A (ja) * | 1986-05-26 | 1987-12-02 | 株式会社ジーシー | 歯面保護用塗布材 |
| US4957441A (en) * | 1988-12-20 | 1990-09-18 | Minnesota Mining And Manufacturing Company | Method of enhancing the curing of a photocurable dental restorative material |
-
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
Also Published As
| Publication number | Publication date |
|---|---|
| DE3939998C2 (enExample) | 1993-02-11 |
| DE59007387D1 (de) | 1994-11-10 |
| ATE112483T1 (de) | 1994-10-15 |
| 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 |
| AU629432B2 (en) | 1992-10-01 |
| AU6767090A (en) | 1991-06-06 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| CA2031268C (en) | Process for the optical distinction of a dental material and dental material for said process | |
| CN101557791B (zh) | 使用具有酸性组分和可光漂白染料的牙科用组合物的方法 | |
| JP4093764B2 (ja) | サーモクロミック歯科材料 | |
| US6149895A (en) | Dental bleaching compositions, kits & methods | |
| AU681556B2 (en) | Photochromic dental material | |
| JP4498501B2 (ja) | 歯科用グラスアイオノマーセメント組成物 | |
| AU701111B2 (en) | Universal water-based medical and dental cement | |
| EP0906076B1 (en) | Glass ionomer cement | |
| US5814682A (en) | Method of luting a provisional prosthetic device using a glass ionomer cement system and kit therefor | |
| BRPI0914427B1 (pt) | composição dental endurecivel | |
| US4600389A (en) | Dental restoration method and composition therefor | |
| CA2432901A1 (en) | Dental materials | |
| CN101351182A (zh) | 牙科用组合物和具有多环芳族组分的引发剂体系 | |
| US10980712B2 (en) | Photochromic dental material with encapsulated photochromic colorants | |
| JPH05132409A (ja) | 光硬化性歯科用修復材組成物 | |
| EP0836468B1 (en) | Method of luting a provisional prosthetic device using a glass ionomer cement system and kit therefor | |
| CA2077943C (en) | Aesthetic, opalescent cold-polymerizable dental restorative | |
| US20070065780A1 (en) | Composite paste for dental prostheses | |
| AU696562B2 (en) | Aesthetic, opalescent cold-polymerizable dental restorative | |
| WO2025057131A1 (en) | Curable dental compositions with extended calcium, hydroxide, and enhanced fluoride release | |
| Al Marhubi | Monomer conversion and colour of antibacterial, remineralising dental composites | |
| KR100932889B1 (ko) | 광에 의해 색상이 변화하는 색소를 포함하는 치과용 조성물 | |
| Haggag et al. | AL-AZHAR | |
| FR2892301A1 (fr) | Tenon dentaire en materiau composite ou ciment ou composite pigmente |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| EEER | Examination request | ||
| MKLA | Lapsed |