AU772056B2 - Polyether based preparation and the use thereof - Google Patents
Polyether based preparation and the use thereof Download PDFInfo
- Publication number
- AU772056B2 AU772056B2 AU25160/01A AU2516001A AU772056B2 AU 772056 B2 AU772056 B2 AU 772056B2 AU 25160/01 A AU25160/01 A AU 25160/01A AU 2516001 A AU2516001 A AU 2516001A AU 772056 B2 AU772056 B2 AU 772056B2
- Authority
- AU
- Australia
- Prior art keywords
- constituent
- compounds
- polyether
- preparation
- type
- 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
- 229920000570 polyether Polymers 0.000 title claims abstract description 70
- 238000002360 preparation method Methods 0.000 title claims abstract description 60
- 239000004721 Polyphenylene oxide Substances 0.000 title claims abstract description 46
- 150000001875 compounds Chemical class 0.000 claims abstract description 30
- 239000000470 constituent Substances 0.000 claims abstract description 28
- 239000005548 dental material Substances 0.000 claims abstract description 25
- 125000004122 cyclic group Chemical group 0.000 claims abstract description 16
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims abstract description 15
- 239000004480 active ingredient Substances 0.000 claims abstract description 10
- 230000000694 effects Effects 0.000 claims abstract description 9
- 239000000945 filler Substances 0.000 claims abstract description 7
- 241001465754 Metazoa Species 0.000 claims abstract description 4
- 239000000203 mixture Substances 0.000 claims description 17
- 239000003925 fat Substances 0.000 claims description 14
- 150000002148 esters Chemical class 0.000 claims description 12
- -1 oxytetramethylene Chemical group 0.000 claims description 12
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 9
- 239000004014 plasticizer Substances 0.000 claims description 9
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 7
- 229920000642 polymer Polymers 0.000 claims description 7
- 229920005862 polyol Polymers 0.000 claims description 7
- 150000003077 polyols Chemical class 0.000 claims description 7
- PKQYSCBUFZOAPE-UHFFFAOYSA-N 1,2-dibenzyl-3-methylbenzene Chemical compound C=1C=CC=CC=1CC=1C(C)=CC=CC=1CC1=CC=CC=C1 PKQYSCBUFZOAPE-UHFFFAOYSA-N 0.000 claims description 6
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 claims description 6
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 claims description 6
- 235000012239 silicon dioxide Nutrition 0.000 claims description 6
- 239000005909 Kieselgur Substances 0.000 claims description 5
- 125000003118 aryl group Chemical group 0.000 claims description 5
- 150000004292 cyclic ethers Chemical class 0.000 claims description 4
- 229920001451 polypropylene glycol Polymers 0.000 claims description 4
- 230000001698 pyrogenic effect Effects 0.000 claims description 4
- 125000005624 silicic acid group Chemical class 0.000 claims description 4
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 claims description 3
- 239000002253 acid Substances 0.000 claims description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 3
- 229920000728 polyester Polymers 0.000 claims description 3
- 229920006389 polyphenyl polymer Polymers 0.000 claims description 3
- VXRUADVCBZMFSV-UHFFFAOYSA-N 2-acetyloxypropane-1,2,3-tricarboxylic acid Chemical compound CC(=O)OC(CC(O)=O)(CC(O)=O)C(O)=O VXRUADVCBZMFSV-UHFFFAOYSA-N 0.000 claims description 2
- 240000007594 Oryza sativa Species 0.000 claims description 2
- 235000007164 Oryza sativa Nutrition 0.000 claims description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 2
- 125000002252 acyl group Chemical group 0.000 claims description 2
- 125000000217 alkyl group Chemical group 0.000 claims description 2
- SAOKZLXYCUGLFA-UHFFFAOYSA-N bis(2-ethylhexyl) adipate Chemical compound CCCCC(CC)COC(=O)CCCCC(=O)OCC(CC)CCCC SAOKZLXYCUGLFA-UHFFFAOYSA-N 0.000 claims description 2
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 2
- 150000001991 dicarboxylic acids Chemical class 0.000 claims description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 2
- 239000004417 polycarbonate Substances 0.000 claims description 2
- 229920000515 polycarbonate Polymers 0.000 claims description 2
- 229920000098 polyolefin Polymers 0.000 claims description 2
- 229920002635 polyurethane Polymers 0.000 claims description 2
- 239000004814 polyurethane Substances 0.000 claims description 2
- 235000009566 rice Nutrition 0.000 claims description 2
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims description 2
- 125000000218 acetic acid group Chemical group C(C)(=O)* 0.000 claims 2
- HIXDQWDOVZUNNA-UHFFFAOYSA-N 2-(3,4-dimethoxyphenyl)-5-hydroxy-7-methoxychromen-4-one Chemical compound C=1C(OC)=CC(O)=C(C(C=2)=O)C=1OC=2C1=CC=C(OC)C(OC)=C1 HIXDQWDOVZUNNA-UHFFFAOYSA-N 0.000 claims 1
- 150000001491 aromatic compounds Chemical class 0.000 claims 1
- 230000000052 comparative effect Effects 0.000 claims 1
- 150000003022 phthalic acids Chemical class 0.000 claims 1
- 239000000463 material Substances 0.000 description 22
- 235000019197 fats Nutrition 0.000 description 13
- 239000003054 catalyst Substances 0.000 description 12
- 238000000034 method Methods 0.000 description 12
- 239000011505 plaster Substances 0.000 description 11
- 239000003921 oil Substances 0.000 description 9
- 235000019198 oils Nutrition 0.000 description 9
- 239000000126 substance Substances 0.000 description 9
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 8
- 238000011156 evaluation Methods 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- 238000010348 incorporation Methods 0.000 description 5
- 230000008569 process Effects 0.000 description 5
- 206010017076 Fracture Diseases 0.000 description 4
- 238000004040 coloring Methods 0.000 description 4
- 239000007858 starting material Substances 0.000 description 4
- QZCLKYGREBVARF-UHFFFAOYSA-N Acetyl tributyl citrate Chemical group CCCCOC(=O)CC(C(=O)OCCCC)(OC(C)=O)CC(=O)OCCCC QZCLKYGREBVARF-UHFFFAOYSA-N 0.000 description 3
- 208000010392 Bone Fractures Diseases 0.000 description 3
- 235000019482 Palm oil Nutrition 0.000 description 3
- 235000014121 butter Nutrition 0.000 description 3
- 238000007306 functionalization reaction Methods 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000002540 palm oil Substances 0.000 description 3
- 239000004033 plastic Substances 0.000 description 3
- 229920003023 plastic Polymers 0.000 description 3
- 238000003860 storage Methods 0.000 description 3
- 239000004094 surface-active agent Substances 0.000 description 3
- 239000003760 tallow Substances 0.000 description 3
- 150000003626 triacylglycerols Chemical class 0.000 description 3
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 2
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 2
- 235000019568 aromas Nutrition 0.000 description 2
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 2
- 229920001400 block copolymer Polymers 0.000 description 2
- 238000005266 casting Methods 0.000 description 2
- 238000012512 characterization method Methods 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000013461 design Methods 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 229920001971 elastomer Polymers 0.000 description 2
- 239000000806 elastomer Substances 0.000 description 2
- 229910052740 iodine Inorganic materials 0.000 description 2
- 239000011630 iodine Substances 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- 230000009467 reduction Effects 0.000 description 2
- RMAQACBXLXPBSY-UHFFFAOYSA-N silicic acid Chemical class O[Si](O)(O)O RMAQACBXLXPBSY-UHFFFAOYSA-N 0.000 description 2
- 235000012424 soybean oil Nutrition 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- LEHNQGSPRXHYRT-UHFFFAOYSA-N 2-dodecyl-1h-imidazole Chemical compound CCCCCCCCCCCCC1=NC=CN1 LEHNQGSPRXHYRT-UHFFFAOYSA-N 0.000 description 1
- HBTAOSGHCXUEKI-UHFFFAOYSA-N 4-chloro-n,n-dimethyl-3-nitrobenzenesulfonamide Chemical compound CN(C)S(=O)(=O)C1=CC=C(Cl)C([N+]([O-])=O)=C1 HBTAOSGHCXUEKI-UHFFFAOYSA-N 0.000 description 1
- 240000004507 Abelmoschus esculentus Species 0.000 description 1
- 235000006667 Aleurites moluccana Nutrition 0.000 description 1
- 229910015900 BF3 Inorganic materials 0.000 description 1
- 235000003301 Ceiba pentandra Nutrition 0.000 description 1
- 244000146553 Ceiba pentandra Species 0.000 description 1
- 241000251730 Chondrichthyes Species 0.000 description 1
- 102100028717 Cytosolic 5'-nucleotidase 3A Human genes 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 239000004150 EU approved colour Substances 0.000 description 1
- 241000196324 Embryophyta Species 0.000 description 1
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 description 1
- 239000005977 Ethylene Substances 0.000 description 1
- 240000000797 Hibiscus cannabinus Species 0.000 description 1
- 206010053317 Hydrophobia Diseases 0.000 description 1
- 241000219745 Lupinus Species 0.000 description 1
- 235000008753 Papaver somniferum Nutrition 0.000 description 1
- 240000001090 Papaver somniferum Species 0.000 description 1
- 235000019483 Peanut oil Nutrition 0.000 description 1
- 235000004347 Perilla Nutrition 0.000 description 1
- 244000124853 Perilla frutescens Species 0.000 description 1
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
- 239000004743 Polypropylene Substances 0.000 description 1
- 206010037742 Rabies Diseases 0.000 description 1
- 235000019484 Rapeseed oil Nutrition 0.000 description 1
- 235000019485 Safflower oil Nutrition 0.000 description 1
- 235000019486 Sunflower oil Nutrition 0.000 description 1
- 238000006887 Ullmann reaction Methods 0.000 description 1
- 235000018936 Vitellaria paradoxa Nutrition 0.000 description 1
- 241001135917 Vitellaria paradoxa Species 0.000 description 1
- 240000008042 Zea mays Species 0.000 description 1
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 1
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- 235000021302 avocado oil Nutrition 0.000 description 1
- 239000008163 avocado oil Substances 0.000 description 1
- 235000015278 beef Nutrition 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- WTEOIRVLGSZEPR-UHFFFAOYSA-N boron trifluoride Chemical compound FB(F)F WTEOIRVLGSZEPR-UHFFFAOYSA-N 0.000 description 1
- 244000192479 candlenut Species 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 229940031578 diisopropyl adipate Drugs 0.000 description 1
- CNHQWLUGXFIDAT-UHFFFAOYSA-N dioctyl 2-hydroxybutanedioate Chemical compound CCCCCCCCOC(=O)CC(O)C(=O)OCCCCCCCC CNHQWLUGXFIDAT-UHFFFAOYSA-N 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- 235000019387 fatty acid methyl ester Nutrition 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 125000005456 glyceride group Chemical group 0.000 description 1
- 150000002314 glycerols Chemical class 0.000 description 1
- 239000008169 grapeseed oil Substances 0.000 description 1
- 239000010460 hemp oil Substances 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 229910003480 inorganic solid Inorganic materials 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 235000009973 maize Nutrition 0.000 description 1
- 210000004379 membrane Anatomy 0.000 description 1
- 239000012528 membrane Substances 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 210000004400 mucous membrane Anatomy 0.000 description 1
- 239000004006 olive oil Substances 0.000 description 1
- 235000008390 olive oil Nutrition 0.000 description 1
- 229940006093 opthalmologic coloring agent diagnostic Drugs 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 239000000312 peanut oil Substances 0.000 description 1
- 230000003239 periodontal effect Effects 0.000 description 1
- 150000003021 phthalic acid derivatives Chemical class 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920001155 polypropylene Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 239000008171 pumpkin seed oil Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 235000005713 safflower oil Nutrition 0.000 description 1
- 239000003813 safflower oil Substances 0.000 description 1
- 210000003296 saliva Anatomy 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000008159 sesame oil Substances 0.000 description 1
- 235000011803 sesame oil Nutrition 0.000 description 1
- 229940057910 shea butter Drugs 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 125000003696 stearoyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 239000004575 stone Substances 0.000 description 1
- 238000005728 strengthening Methods 0.000 description 1
- 150000003459 sulfonic acid esters Chemical class 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000002600 sunflower oil Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- DCXXMTOCNZCJGO-UHFFFAOYSA-N tristearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(OC(=O)CCCCCCCCCCCCCCCCC)COC(=O)CCCCCCCCCCCCCCCCC DCXXMTOCNZCJGO-UHFFFAOYSA-N 0.000 description 1
- 239000002383 tung oil Substances 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000010497 wheat germ oil Substances 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
- A61K6/90—Compositions for taking dental impressions
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)
- Dental Preparations (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10001747 | 2000-01-17 | ||
| DE10001747A DE10001747C2 (de) | 2000-01-17 | 2000-01-17 | Zubereitungen auf Polyetherbasis und deren Verwendung |
| PCT/EP2001/000395 WO2001052792A1 (de) | 2000-01-17 | 2001-01-15 | Zubereitungen auf polyetherbasis und deren verwendung |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| AU2516001A AU2516001A (en) | 2001-07-31 |
| AU772056B2 true AU772056B2 (en) | 2004-04-08 |
Family
ID=7627782
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AU25160/01A Ceased AU772056B2 (en) | 2000-01-17 | 2001-01-15 | Polyether based preparation and the use thereof |
Country Status (7)
| Country | Link |
|---|---|
| US (1) | US6919386B2 (https=) |
| EP (1) | EP1248588B1 (https=) |
| JP (1) | JP2003520216A (https=) |
| AT (1) | ATE295142T1 (https=) |
| AU (1) | AU772056B2 (https=) |
| DE (2) | DE10001747C2 (https=) |
| WO (1) | WO2001052792A1 (https=) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10235990A1 (de) | 2002-08-06 | 2004-02-26 | 3M Espe Ag | Zubereitungen auf Polyetherbasis und deren Verwendung |
| DE60300415T2 (de) * | 2003-07-17 | 2006-03-09 | 3M Espe Ag | Dentalzusammensetzungen mit Ethyleniminverbindungen und nicht-reaktiven Beschleunigern |
| WO2005072683A1 (en) * | 2004-01-21 | 2005-08-11 | 3M Innovative Properties Company | Dental compositions and kits containing bitterness inhibitors, and related methods |
| EP1787627A1 (en) * | 2005-11-17 | 2007-05-23 | 3M Innovative Properties Company | Anti-microbial dental impression material |
| EP1820815A1 (en) * | 2006-02-15 | 2007-08-22 | 3M Innovative Properties Company | Composition containing aziridino groups and use thereof |
| EP1865014A1 (en) | 2006-06-07 | 2007-12-12 | 3M Innovative Properties Company | Composition containing aziridino groups, method of production and use thereof |
| EP1882469A1 (en) * | 2006-07-28 | 2008-01-30 | 3M Innovative Properties Company | Polyether-based preparations and use thereof |
| EP2428199A1 (en) | 2010-09-09 | 2012-03-14 | 3M Innovative Properties Company | Curable composition, process of production and use thereof |
| US8752287B2 (en) | 2011-04-07 | 2014-06-17 | Melvin James Daniels | Method of sealing at least one engine gas leak |
| DE102013008176A1 (de) | 2012-10-05 | 2014-04-10 | Voco Gmbh | Kit und Verfahren zur indirekten chairside Herstellung von Kompositinlays |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3246654A1 (de) * | 1982-12-16 | 1984-06-20 | ESPE Fabrik pharmazeutischer Präparate GmbH, 8031 Seefeld | Nichtadhaesive abdruckmasse |
| DE19711514A1 (de) * | 1997-03-19 | 1998-09-24 | Thera Ges Fuer Patente | Triglyceride enthaltende Abformmassen |
| DE19740234A1 (de) * | 1997-09-12 | 1999-03-18 | Espe Dental Ag | Dentalmassen auf Polyetherbasis |
Family Cites Families (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1745810B2 (de) | 1963-05-29 | 1971-12-02 | Espe Fabrik pharmazeutischer Prapa rate GmbH, 8031 Seefeld | Verfahren zur herstellung von formkoerpern auf der basis von aethyleniminverbindungen |
| DE3245052A1 (de) | 1982-12-06 | 1984-06-07 | ESPE Fabrik pharmazeutischer Präparate GmbH, 8031 Seefeld | Verzoegerer fuer die polymerisation von aziridinverbindungen |
| DE3932989A1 (de) * | 1989-10-03 | 1991-04-11 | Espe Stiftung | Polyalkylenoxidderivate enthaltende polyetherabformmassen |
| DE19505896A1 (de) * | 1995-02-21 | 1996-08-22 | Heijo Dr Huebner | Leicht anmischbare Abformmasse mit hoher Zeichnungsschärfe |
| DE19942459A1 (de) * | 1999-09-06 | 2001-03-15 | Espe Dental Ag | Elastomermassen mit verbesserter Katalysatorkomponente |
-
2000
- 2000-01-17 DE DE10001747A patent/DE10001747C2/de not_active Expired - Fee Related
-
2001
- 2001-01-15 DE DE50106198T patent/DE50106198D1/de not_active Expired - Lifetime
- 2001-01-15 EP EP01900446A patent/EP1248588B1/de not_active Expired - Lifetime
- 2001-01-15 US US10/181,358 patent/US6919386B2/en not_active Expired - Lifetime
- 2001-01-15 AT AT01900446T patent/ATE295142T1/de not_active IP Right Cessation
- 2001-01-15 JP JP2001552842A patent/JP2003520216A/ja not_active Withdrawn
- 2001-01-15 AU AU25160/01A patent/AU772056B2/en not_active Ceased
- 2001-01-15 WO PCT/EP2001/000395 patent/WO2001052792A1/de not_active Ceased
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3246654A1 (de) * | 1982-12-16 | 1984-06-20 | ESPE Fabrik pharmazeutischer Präparate GmbH, 8031 Seefeld | Nichtadhaesive abdruckmasse |
| DE19711514A1 (de) * | 1997-03-19 | 1998-09-24 | Thera Ges Fuer Patente | Triglyceride enthaltende Abformmassen |
| DE19740234A1 (de) * | 1997-09-12 | 1999-03-18 | Espe Dental Ag | Dentalmassen auf Polyetherbasis |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2003520216A (ja) | 2003-07-02 |
| WO2001052792A1 (de) | 2001-07-26 |
| DE50106198D1 (de) | 2005-06-16 |
| US20030109596A1 (en) | 2003-06-12 |
| EP1248588A1 (de) | 2002-10-16 |
| ATE295142T1 (de) | 2005-05-15 |
| US6919386B2 (en) | 2005-07-19 |
| DE10001747A1 (de) | 2001-07-26 |
| DE10001747C2 (de) | 2003-02-13 |
| EP1248588B1 (de) | 2005-05-11 |
| AU2516001A (en) | 2001-07-31 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FGA | Letters patent sealed or granted (standard patent) |