NL8102128A - Polymeriseerbaar mengsel voor tandheelkundige toepassing, alsmede werkwijze voor het bereiden daarvan. - Google Patents
Polymeriseerbaar mengsel voor tandheelkundige toepassing, alsmede werkwijze voor het bereiden daarvan. Download PDFInfo
- Publication number
- NL8102128A NL8102128A NL8102128A NL8102128A NL8102128A NL 8102128 A NL8102128 A NL 8102128A NL 8102128 A NL8102128 A NL 8102128A NL 8102128 A NL8102128 A NL 8102128A NL 8102128 A NL8102128 A NL 8102128A
- Authority
- NL
- Netherlands
- Prior art keywords
- monomer
- mixture according
- mixture
- cupric
- reducing agent
- Prior art date
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- 239000000203 mixture Substances 0.000 title claims description 78
- 238000000034 method Methods 0.000 title claims description 9
- 238000002360 preparation method Methods 0.000 title description 2
- 239000000178 monomer Substances 0.000 claims description 50
- 239000003638 chemical reducing agent Substances 0.000 claims description 28
- -1 peroxy compound Chemical class 0.000 claims description 26
- 150000001875 compounds Chemical class 0.000 claims description 18
- 239000003054 catalyst Substances 0.000 claims description 17
- 238000006116 polymerization reaction Methods 0.000 claims description 17
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 15
- 239000000945 filler Substances 0.000 claims description 11
- 150000002500 ions Chemical class 0.000 claims description 11
- JPVYNHNXODAKFH-UHFFFAOYSA-N Cu2+ Chemical compound [Cu+2] JPVYNHNXODAKFH-UHFFFAOYSA-N 0.000 claims description 10
- OPQARKPSCNTWTJ-UHFFFAOYSA-L copper(ii) acetate Chemical compound [Cu+2].CC([O-])=O.CC([O-])=O OPQARKPSCNTWTJ-UHFFFAOYSA-L 0.000 claims description 10
- ORTQZVOHEJQUHG-UHFFFAOYSA-L copper(II) chloride Chemical compound Cl[Cu]Cl ORTQZVOHEJQUHG-UHFFFAOYSA-L 0.000 claims description 8
- 239000000047 product Substances 0.000 claims description 8
- 239000006087 Silane Coupling Agent Substances 0.000 claims description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Natural products NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 5
- 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 claims description 5
- 229940076286 cupric acetate Drugs 0.000 claims description 5
- IPCRBOOJBPETMF-UHFFFAOYSA-N N-acetylthiourea Chemical group CC(=O)NC(N)=S IPCRBOOJBPETMF-UHFFFAOYSA-N 0.000 claims description 4
- HTKFORQRBXIQHD-UHFFFAOYSA-N allylthiourea Chemical compound NC(=S)NCC=C HTKFORQRBXIQHD-UHFFFAOYSA-N 0.000 claims description 4
- 229960001748 allylthiourea Drugs 0.000 claims description 4
- UMGDCJDMYOKAJW-UHFFFAOYSA-N aminothiocarboxamide Natural products NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 claims description 4
- 229960003280 cupric chloride Drugs 0.000 claims description 4
- 239000002685 polymerization catalyst Substances 0.000 claims description 4
- 230000003213 activating effect Effects 0.000 claims description 3
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- 150000003254 radicals Chemical class 0.000 claims description 3
- ONIKNECPXCLUHT-UHFFFAOYSA-N 2-chlorobenzoyl chloride Chemical compound ClC(=O)C1=CC=CC=C1Cl ONIKNECPXCLUHT-UHFFFAOYSA-N 0.000 claims description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 2
- SAPGBCWOQLHKKZ-UHFFFAOYSA-N 6-(2-methylprop-2-enoyloxy)hexyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCCCCOC(=O)C(C)=C SAPGBCWOQLHKKZ-UHFFFAOYSA-N 0.000 claims description 2
- 239000007795 chemical reaction product Substances 0.000 claims description 2
- QYJPSWYYEKYVEJ-FDGPNNRMSA-L copper;(z)-4-oxopent-2-en-2-olate Chemical compound [Cu+2].C\C([O-])=C\C(C)=O.C\C([O-])=C\C(C)=O QYJPSWYYEKYVEJ-FDGPNNRMSA-L 0.000 claims description 2
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- 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 5
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- 239000002253 acid Substances 0.000 description 3
- OXBLHERUFWYNTN-UHFFFAOYSA-M copper(I) chloride Chemical compound [Cu]Cl OXBLHERUFWYNTN-UHFFFAOYSA-M 0.000 description 3
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 3
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- 125000002252 acyl group Chemical group 0.000 description 2
- 229910021486 amorphous silicon dioxide Inorganic materials 0.000 description 2
- 125000003710 aryl alkyl group Chemical group 0.000 description 2
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- 229910052788 barium Inorganic materials 0.000 description 2
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- UCGFRIAOVLXVKL-UHFFFAOYSA-N benzylthiourea Chemical compound NC(=S)NCC1=CC=CC=C1 UCGFRIAOVLXVKL-UHFFFAOYSA-N 0.000 description 2
- GMEGXJPUFRVCPX-UHFFFAOYSA-N butylthiourea Chemical compound CCCCNC(N)=S GMEGXJPUFRVCPX-UHFFFAOYSA-N 0.000 description 2
- 229910052793 cadmium Inorganic materials 0.000 description 2
- BDOSMKKIYDKNTQ-UHFFFAOYSA-N cadmium atom Chemical compound [Cd] BDOSMKKIYDKNTQ-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 125000002603 chloroethyl group Chemical group [H]C([*])([H])C([H])([H])Cl 0.000 description 2
- 229940075614 colloidal silicon dioxide Drugs 0.000 description 2
- SPTHWAJJMLCAQF-UHFFFAOYSA-M ctk4f8481 Chemical compound [O-]O.CC(C)C1=CC=CC=C1C(C)C SPTHWAJJMLCAQF-UHFFFAOYSA-M 0.000 description 2
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- 239000001257 hydrogen Substances 0.000 description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 2
- QUPCNWFFTANZPX-UHFFFAOYSA-N hydrogen peroxide;1-methyl-4-propan-2-ylcyclohexane Chemical compound OO.CC(C)C1CCC(C)CC1 QUPCNWFFTANZPX-UHFFFAOYSA-N 0.000 description 2
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 2
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- BHJYKFUCQNISJA-UHFFFAOYSA-N (3-hydroxyphenyl)thiourea Chemical compound NC(=S)NC1=CC=CC(O)=C1 BHJYKFUCQNISJA-UHFFFAOYSA-N 0.000 description 1
- NQKRXWYQYPNMCO-UHFFFAOYSA-N (4-methylphenyl)sulfonylthiourea Chemical compound CC1=CC=C(S(=O)(=O)NC(N)=S)C=C1 NQKRXWYQYPNMCO-UHFFFAOYSA-N 0.000 description 1
- JAEZSIYNWDWMMN-UHFFFAOYSA-N 1,1,3-trimethylthiourea Chemical compound CNC(=S)N(C)C JAEZSIYNWDWMMN-UHFFFAOYSA-N 0.000 description 1
- OVRQXQSDQWOJIL-UHFFFAOYSA-N 1,1-dibutylthiourea Chemical compound CCCCN(C(N)=S)CCCC OVRQXQSDQWOJIL-UHFFFAOYSA-N 0.000 description 1
- QADMBPYDNAHONY-UHFFFAOYSA-N 1,1-diethyl-3-prop-2-enylthiourea Chemical compound CCN(CC)C(=S)NCC=C QADMBPYDNAHONY-UHFFFAOYSA-N 0.000 description 1
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- 125000001140 1,4-phenylene group Chemical group [H]C1=C([H])C([*:2])=C([H])C([H])=C1[*:1] 0.000 description 1
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- NGNBDVOYPDDBFK-UHFFFAOYSA-N 2-[2,4-di(pentan-2-yl)phenoxy]acetyl chloride Chemical class CCCC(C)C1=CC=C(OCC(Cl)=O)C(C(C)CCC)=C1 NGNBDVOYPDDBFK-UHFFFAOYSA-N 0.000 description 1
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- JPYHHZQJCSQRJY-UHFFFAOYSA-N Phloroglucinol Natural products CCC=CCC=CCC=CCC=CCCCCC(=O)C1=C(O)C=C(O)C=C1O JPYHHZQJCSQRJY-UHFFFAOYSA-N 0.000 description 1
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 description 1
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- 238000009835 boiling Methods 0.000 description 1
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- ARUVKPQLZAKDPS-UHFFFAOYSA-L copper(II) sulfate Chemical compound [Cu+2].[O-][S+2]([O-])([O-])[O-] ARUVKPQLZAKDPS-UHFFFAOYSA-L 0.000 description 1
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- DCUFMVPCXCSVNP-UHFFFAOYSA-N methacrylic anhydride Chemical compound CC(=C)C(=O)OC(=O)C(C)=C DCUFMVPCXCSVNP-UHFFFAOYSA-N 0.000 description 1
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- 238000012544 monitoring process Methods 0.000 description 1
- LPEAMLCGSMPLLI-UHFFFAOYSA-N n-(2-sulfanylethylcarbamothioyl)acetamide Chemical compound CC(=O)NC(=S)NCCS LPEAMLCGSMPLLI-UHFFFAOYSA-N 0.000 description 1
- DQMWMUMCNOJLSI-UHFFFAOYSA-N n-carbamothioylbenzamide Chemical compound NC(=S)NC(=O)C1=CC=CC=C1 DQMWMUMCNOJLSI-UHFFFAOYSA-N 0.000 description 1
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- 125000002801 octanoyl group Chemical group C(CCCCCCC)(=O)* 0.000 description 1
- 125000002347 octyl group Chemical group [H]C([*])([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
- QAKUNEDFMJPMGO-UHFFFAOYSA-N octylthiourea Chemical compound CCCCCCCCNC(N)=S QAKUNEDFMJPMGO-UHFFFAOYSA-N 0.000 description 1
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- QCDYQQDYXPDABM-UHFFFAOYSA-N phloroglucinol Chemical compound OC1=CC(O)=CC(O)=C1 QCDYQQDYXPDABM-UHFFFAOYSA-N 0.000 description 1
- 229960001553 phloroglucinol Drugs 0.000 description 1
- 230000000704 physical effect Effects 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 239000003495 polar organic solvent Substances 0.000 description 1
- 239000010453 quartz Substances 0.000 description 1
- 230000009257 reactivity Effects 0.000 description 1
- 239000005368 silicate glass Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 238000001179 sorption measurement Methods 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 230000000087 stabilizing effect Effects 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- CIOAGBVUUVVLOB-UHFFFAOYSA-N strontium atom Chemical compound [Sr] CIOAGBVUUVVLOB-UHFFFAOYSA-N 0.000 description 1
- 125000000547 substituted alkyl group Chemical group 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical group [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- 239000004408 titanium dioxide Substances 0.000 description 1
- 125000005628 tolylene group Chemical class 0.000 description 1
- GQIUQDDJKHLHTB-UHFFFAOYSA-N trichloro(ethenyl)silane Chemical compound Cl[Si](Cl)(Cl)C=C GQIUQDDJKHLHTB-UHFFFAOYSA-N 0.000 description 1
- 239000005050 vinyl trichlorosilane Substances 0.000 description 1
- UKRDPEFKFJNXQM-UHFFFAOYSA-N vinylsilane Chemical compound [SiH3]C=C UKRDPEFKFJNXQM-UHFFFAOYSA-N 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 235000014692 zinc oxide Nutrition 0.000 description 1
- RNWHGQJWIACOKP-UHFFFAOYSA-N zinc;oxygen(2-) Chemical class [O-2].[Zn+2] RNWHGQJWIACOKP-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F4/00—Polymerisation catalysts
- C08F4/40—Redox systems
-
- 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)
- Chemical & Material Sciences (AREA)
- Oral & Maxillofacial Surgery (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Plastic & Reconstructive Surgery (AREA)
- Life Sciences & Earth Sciences (AREA)
- Materials Engineering (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Dental Preparations (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US14519980A | 1980-04-29 | 1980-04-29 | |
| US14519980 | 1980-04-29 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8102128A true NL8102128A (nl) | 1981-11-16 |
Family
ID=22512027
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8102128A NL8102128A (nl) | 1980-04-29 | 1981-04-29 | Polymeriseerbaar mengsel voor tandheelkundige toepassing, alsmede werkwijze voor het bereiden daarvan. |
Country Status (20)
| Country | Link |
|---|---|
| JP (1) | JPS56169609A (enExample) |
| AT (1) | AT376125B (enExample) |
| AU (1) | AU554532B2 (enExample) |
| BE (1) | BE888599A (enExample) |
| BR (1) | BR8102607A (enExample) |
| CA (1) | CA1223696A (enExample) |
| CH (1) | CH649465A5 (enExample) |
| DE (1) | DE3116132A1 (enExample) |
| DK (1) | DK157727B (enExample) |
| ES (1) | ES501695A0 (enExample) |
| FR (1) | FR2481114A1 (enExample) |
| GB (2) | GB2075035B (enExample) |
| IE (1) | IE51152B1 (enExample) |
| MX (1) | MX156002A (enExample) |
| NL (1) | NL8102128A (enExample) |
| NO (1) | NO158991C (enExample) |
| NZ (1) | NZ196864A (enExample) |
| PH (1) | PH17044A (enExample) |
| SE (1) | SE450547B (enExample) |
| ZA (1) | ZA812567B (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3928987A1 (de) * | 1989-09-01 | 1991-03-28 | Siegfried Reiss | Verfahren und formmasse zur herstellung von formlingen fuer den dentalbereich |
| DE4339399A1 (de) * | 1993-11-18 | 1995-05-24 | Thera Ges Fuer Patente | Durch Polymerisation einer ethylenisch polymerisierbaren Masse in Formen hergestellte Formkörper (Inserts) |
| US20070100019A1 (en) * | 2005-08-02 | 2007-05-03 | Fuming Sun | Catalyst system for dental compositions |
| DE102005039590B4 (de) * | 2005-08-19 | 2008-05-21 | Heraeus Kulzer Gmbh | Polymerisierbare Dentalzusammensetzung mit einem 2-Komponenten-Initiatorsystem |
| EP1849449A1 (en) | 2006-04-26 | 2007-10-31 | 3M Innovative Properties Company | Filler containing composition and process for production and use thereof |
| WO2008134024A2 (en) * | 2007-04-25 | 2008-11-06 | Dentsply International Inc. | Self-adhesive dental cement |
| JP2009292761A (ja) * | 2008-06-04 | 2009-12-17 | Kuraray Medical Inc | 歯科用硬化性組成物 |
| JP5388482B2 (ja) * | 2008-06-04 | 2014-01-15 | クラレノリタケデンタル株式会社 | 歯科用硬化性組成物 |
| CN102702405B (zh) * | 2012-07-05 | 2014-04-09 | 东营市诺尔化工有限责任公司 | 一种超低残留吸水树脂的制备方法 |
| JP6112887B2 (ja) * | 2013-02-05 | 2017-04-12 | 株式会社トクヤマデンタル | 歯科用硬化性組成物 |
| JP6086797B2 (ja) * | 2013-04-25 | 2017-03-01 | クラレノリタケデンタル株式会社 | 歯科用重合性組成物 |
| CA2954628A1 (en) | 2014-07-10 | 2016-01-14 | 3M Innovative Properties Company | Two-component self-adhesive dental composition, process of production and use thereof |
| JP2018504447A (ja) * | 2015-02-09 | 2018-02-15 | ゼスト、アイピー、ホールディングス、リミテッド、ライアビリティー、カンパニーＺｅｓｔ Ｉｐ Ｈｏｌｄｉｎｇｓ，Ｌｌｃ | 歯科用組成物および使用方法 |
| CN111295398B (zh) | 2017-12-26 | 2022-04-26 | 德山齿科株式会社 | 化学聚合引发剂、粘接性组合物及其成套用品以及保管方法、牙科用材料及其成套用品 |
| EP3808324A1 (en) * | 2019-09-26 | 2021-04-21 | Shofu Inc. | Curable composition containing transition metal adsorbent |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB714868A (en) * | 1951-12-24 | 1954-09-01 | Dental Fillings Ltd | Improvements in or relating to polymerisation products |
| GB1177879A (en) * | 1967-09-04 | 1970-01-14 | Sumitomo Chemical Co | Catalyst System and process for the Polymerisation of Vinyl Compounds |
| JPS4842467B1 (enExample) * | 1970-12-04 | 1973-12-12 | ||
| JPS5223509B2 (enExample) * | 1973-04-26 | 1977-06-24 | ||
| JPS587646B2 (ja) * | 1974-05-31 | 1983-02-10 | 東亞合成株式会社 | ニエキセイコウカセイソセイブツ |
| JPS516224A (enExample) * | 1974-07-05 | 1976-01-19 | Johnson & Johnson | |
| US3991008A (en) * | 1974-08-12 | 1976-11-09 | The Kendall Company | Dental compositions having improved color stability |
| JPS51131197A (en) * | 1975-05-08 | 1976-11-15 | Sankin Ind Co | Uniiliquid type dental cement |
-
1981
- 1981-04-16 NZ NZ196864A patent/NZ196864A/en unknown
- 1981-04-16 ZA ZA00812567A patent/ZA812567B/xx unknown
- 1981-04-23 DE DE19813116132 patent/DE3116132A1/de not_active Withdrawn
- 1981-04-27 AT AT0187781A patent/AT376125B/de not_active IP Right Cessation
- 1981-04-27 SE SE8102634A patent/SE450547B/sv not_active IP Right Cessation
- 1981-04-28 ES ES501695A patent/ES501695A0/es active Granted
- 1981-04-28 BE BE0/204628A patent/BE888599A/fr not_active IP Right Cessation
- 1981-04-28 PH PH25567A patent/PH17044A/en unknown
- 1981-04-28 CA CA000376461A patent/CA1223696A/en not_active Expired
- 1981-04-28 FR FR8108413A patent/FR2481114A1/fr active Granted
- 1981-04-28 NO NO811448A patent/NO158991C/no unknown
- 1981-04-28 CH CH2760/81A patent/CH649465A5/de not_active IP Right Cessation
- 1981-04-28 BR BR8102607A patent/BR8102607A/pt unknown
- 1981-04-28 AU AU69911/81A patent/AU554532B2/en not_active Ceased
- 1981-04-29 NL NL8102128A patent/NL8102128A/nl not_active Application Discontinuation
- 1981-04-29 IE IE958/81A patent/IE51152B1/en unknown
- 1981-04-29 MX MX187116A patent/MX156002A/es unknown
- 1981-04-29 DK DK189781A patent/DK157727B/da not_active Application Discontinuation
- 1981-04-29 GB GB8113265A patent/GB2075035B/en not_active Expired
- 1981-04-30 JP JP6615881A patent/JPS56169609A/ja active Pending
-
1983
- 1983-08-11 GB GB838321611A patent/GB8321611D0/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| BE888599A (fr) | 1981-08-17 |
| NO158991B (no) | 1988-08-15 |
| IE810958L (en) | 1981-10-29 |
| AT376125B (de) | 1984-10-10 |
| DE3116132A1 (de) | 1982-02-04 |
| PH17044A (en) | 1984-05-17 |
| MX156002A (es) | 1988-06-14 |
| ZA812567B (en) | 1982-11-24 |
| DK189781A (da) | 1981-10-30 |
| JPS56169609A (en) | 1981-12-26 |
| SE450547B (sv) | 1987-07-06 |
| SE8102634L (sv) | 1981-10-30 |
| ATA187781A (de) | 1984-03-15 |
| CA1223696A (en) | 1987-06-30 |
| NO811448L (no) | 1981-10-30 |
| ES8206560A1 (es) | 1982-08-16 |
| FR2481114A1 (fr) | 1981-10-30 |
| BR8102607A (pt) | 1982-01-19 |
| AU6991181A (en) | 1981-11-05 |
| DK157727B (da) | 1990-02-12 |
| CH649465A5 (de) | 1985-05-31 |
| GB8321611D0 (en) | 1983-09-14 |
| FR2481114B1 (enExample) | 1984-11-30 |
| GB2075035A (en) | 1981-11-11 |
| GB2075035B (en) | 1984-07-25 |
| IE51152B1 (en) | 1986-10-15 |
| ES501695A0 (es) | 1982-08-16 |
| NO158991C (no) | 1988-11-23 |
| NZ196864A (en) | 1984-04-27 |
| AU554532B2 (en) | 1986-08-28 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| A85 | Still pending on 85-01-01 | ||
| BA | A request for search or an international-type search has been filed | ||
| BB | A search report has been drawn up | ||
| BC | A request for examination has been filed | ||
| BV | The patent application has lapsed |