KR20080012322A - Ｃ.ｉ. 피그먼트 블루-80 계 청색 염료 - Google Patents
Ｃ.ｉ. 피그먼트 블루-80 계 청색 염료 Download PDFInfo
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- KR20080012322A KR20080012322A KR1020077027832A KR20077027832A KR20080012322A KR 20080012322 A KR20080012322 A KR 20080012322A KR 1020077027832 A KR1020077027832 A KR 1020077027832A KR 20077027832 A KR20077027832 A KR 20077027832A KR 20080012322 A KR20080012322 A KR 20080012322A
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- PYKYMHQGRFAEBM-UHFFFAOYSA-N anthraquinone Natural products CCC(=O)c1c(O)c2C(=O)C3C(C=CC=C3O)C(=O)c2cc1CC(=O)OC PYKYMHQGRFAEBM-UHFFFAOYSA-N 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- RJGDLRCDCYRQOQ-UHFFFAOYSA-N anthrone Chemical compound C1=CC=C2C(=O)C3=CC=CC=C3CC2=C1 RJGDLRCDCYRQOQ-UHFFFAOYSA-N 0.000 description 1
- XCZXLLSPCNNZMM-UHFFFAOYSA-N antimony(3+) chromium(3+) oxygen(2-) titanium(4+) Chemical compound [O--].[O--].[O--].[O--].[O--].[Ti+4].[Cr+3].[Sb+3] XCZXLLSPCNNZMM-UHFFFAOYSA-N 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 239000007900 aqueous suspension Substances 0.000 description 1
- IRERQBUNZFJFGC-UHFFFAOYSA-L azure blue Chemical compound [Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Na+].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[Al+3].[S-]S[S-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-].[O-][Si]([O-])([O-])[O-] IRERQBUNZFJFGC-UHFFFAOYSA-L 0.000 description 1
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- ONTQJDKFANPPKK-UHFFFAOYSA-L chembl3185981 Chemical compound [Na+].[Na+].CC1=CC(C)=C(S([O-])(=O)=O)C=C1N=NC1=CC(S([O-])(=O)=O)=C(C=CC=C2)C2=C1O ONTQJDKFANPPKK-UHFFFAOYSA-L 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 150000001805 chlorine compounds Chemical class 0.000 description 1
- 229910000423 chromium oxide Inorganic materials 0.000 description 1
- 229910000428 cobalt oxide Inorganic materials 0.000 description 1
- IVMYJDGYRUAWML-UHFFFAOYSA-N cobalt(ii) oxide Chemical compound [Co]=O IVMYJDGYRUAWML-UHFFFAOYSA-N 0.000 description 1
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- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- PPSZHCXTGRHULJ-UHFFFAOYSA-N dioxazine Chemical compound O1ON=CC=C1 PPSZHCXTGRHULJ-UHFFFAOYSA-N 0.000 description 1
- 239000000982 direct dye Substances 0.000 description 1
- 229940060296 dodecylbenzenesulfonic acid Drugs 0.000 description 1
- 239000010459 dolomite Substances 0.000 description 1
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- 239000000428 dust Substances 0.000 description 1
- 229920001971 elastomer Polymers 0.000 description 1
- 238000004070 electrodeposition Methods 0.000 description 1
- 239000003792 electrolyte Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
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- 150000002118 epoxides Chemical class 0.000 description 1
- 238000005530 etching Methods 0.000 description 1
- VYXSBFYARXAAKO-UHFFFAOYSA-N ethyl 2-[3-(ethylamino)-6-ethylimino-2,7-dimethylxanthen-9-yl]benzoate;hydron;chloride Chemical compound [Cl-].C1=2C=C(C)C(NCC)=CC=2OC2=CC(=[NH+]CC)C(C)=CC2=C1C1=CC=CC=C1C(=O)OCC VYXSBFYARXAAKO-UHFFFAOYSA-N 0.000 description 1
- BHXIWUJLHYHGSJ-UHFFFAOYSA-N ethyl 3-ethoxypropanoate Chemical compound CCOCCC(=O)OCC BHXIWUJLHYHGSJ-UHFFFAOYSA-N 0.000 description 1
- 229920001249 ethyl cellulose Polymers 0.000 description 1
- 235000019325 ethyl cellulose Nutrition 0.000 description 1
- 239000010685 fatty oil Substances 0.000 description 1
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- LNEPOXFFQSENCJ-UHFFFAOYSA-N haloperidol Chemical compound C1CC(O)(C=2C=CC(Cl)=CC=2)CCN1CCCC(=O)C1=CC=C(F)C=C1 LNEPOXFFQSENCJ-UHFFFAOYSA-N 0.000 description 1
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- 150000002462 imidazolines Chemical class 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- UHOKSCJSTAHBSO-UHFFFAOYSA-N indanthrone blue Chemical compound C1=CC=C2C(=O)C3=CC=C4NC5=C6C(=O)C7=CC=CC=C7C(=O)C6=CC=C5NC4=C3C(=O)C2=C1 UHOKSCJSTAHBSO-UHFFFAOYSA-N 0.000 description 1
- AMGQUBHHOARCQH-UHFFFAOYSA-N indium;oxotin Chemical compound [In].[Sn]=O AMGQUBHHOARCQH-UHFFFAOYSA-N 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 239000012948 isocyanate Substances 0.000 description 1
- 150000002513 isocyanates Chemical class 0.000 description 1
- PXZQEOJJUGGUIB-UHFFFAOYSA-N isoindolin-1-one Chemical compound C1=CC=C2C(=O)NCC2=C1 PXZQEOJJUGGUIB-UHFFFAOYSA-N 0.000 description 1
- GWVMLCQWXVFZCN-UHFFFAOYSA-N isoindoline Chemical compound C1=CC=C2CNCC2=C1 GWVMLCQWXVFZCN-UHFFFAOYSA-N 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 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
- 238000004898 kneading Methods 0.000 description 1
- 239000004571 lime Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- 150000002688 maleic acid derivatives Chemical class 0.000 description 1
- 229910052748 manganese Inorganic materials 0.000 description 1
- 230000007246 mechanism Effects 0.000 description 1
- 150000007974 melamines Chemical class 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
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- 230000008018 melting Effects 0.000 description 1
- 239000000434 metal complex dye Substances 0.000 description 1
- 239000010445 mica Substances 0.000 description 1
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- 239000011707 mineral Substances 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- 229910052759 nickel Inorganic materials 0.000 description 1
- 229920001220 nitrocellulos Polymers 0.000 description 1
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- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003921 oil Substances 0.000 description 1
- JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 235000021313 oleic acid Nutrition 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- DGBWPZSGHAXYGK-UHFFFAOYSA-N perinone Chemical compound C12=NC3=CC=CC=C3N2C(=O)C2=CC=C3C4=C2C1=CC=C4C(=O)N1C2=CC=CC=C2N=C13 DGBWPZSGHAXYGK-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
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- 229940104573 pigment red 5 Drugs 0.000 description 1
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- 239000011118 polyvinyl acetate Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920001289 polyvinyl ether Polymers 0.000 description 1
- 150000003141 primary amines Chemical class 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- LLHKCFNBLRBOGN-UHFFFAOYSA-N propylene glycol methyl ether acetate Chemical compound COCC(C)OC(C)=O LLHKCFNBLRBOGN-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- RQGPLDBZHMVWCH-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole Chemical compound C1=NC2=CC=NC2=C1 RQGPLDBZHMVWCH-UHFFFAOYSA-N 0.000 description 1
- FYNROBRQIVCIQF-UHFFFAOYSA-N pyrrolo[3,2-b]pyrrole-5,6-dione Chemical compound C1=CN=C2C(=O)C(=O)N=C21 FYNROBRQIVCIQF-UHFFFAOYSA-N 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000005855 radiation Effects 0.000 description 1
- 150000003254 radicals Chemical class 0.000 description 1
- 239000000985 reactive dye Substances 0.000 description 1
- WPPDXAHGCGPUPK-UHFFFAOYSA-N red 2 Chemical compound C1=CC=CC=C1C(C1=CC=CC=C11)=C(C=2C=3C4=CC=C5C6=CC=C7C8=C(C=9C=CC=CC=9)C9=CC=CC=C9C(C=9C=CC=CC=9)=C8C8=CC=C(C6=C87)C(C=35)=CC=2)C4=C1C1=CC=CC=C1 WPPDXAHGCGPUPK-UHFFFAOYSA-N 0.000 description 1
- 239000001054 red pigment Substances 0.000 description 1
- 229920003987 resole Polymers 0.000 description 1
- 239000005060 rubber Substances 0.000 description 1
- 238000006748 scratching Methods 0.000 description 1
- 230000002393 scratching effect Effects 0.000 description 1
- 150000003335 secondary amines Chemical class 0.000 description 1
- 230000001568 sexual effect Effects 0.000 description 1
- 229920002050 silicone resin Polymers 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
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- 238000009987 spinning Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910001220 stainless steel Inorganic materials 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 229910052712 strontium Inorganic materials 0.000 description 1
- 239000011115 styrene butadiene Substances 0.000 description 1
- 229920003048 styrene butadiene rubber Polymers 0.000 description 1
- 238000000859 sublimation Methods 0.000 description 1
- 230000008022 sublimation Effects 0.000 description 1
- 229940124530 sulfonamide Drugs 0.000 description 1
- 150000003456 sulfonamides Chemical class 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 238000006277 sulfonation reaction Methods 0.000 description 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 description 1
- 239000000988 sulfur dye Substances 0.000 description 1
- 239000000057 synthetic resin Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- JOUDBUYBGJYFFP-FOCLMDBBSA-N thioindigo Chemical compound S\1C2=CC=CC=C2C(=O)C/1=C1/C(=O)C2=CC=CC=C2S1 JOUDBUYBGJYFFP-FOCLMDBBSA-N 0.000 description 1
- AAAQKTZKLRYKHR-UHFFFAOYSA-N triphenylmethane Chemical compound C1=CC=CC=C1C(C=1C=CC=CC=1)C1=CC=CC=C1 AAAQKTZKLRYKHR-UHFFFAOYSA-N 0.000 description 1
- 239000011355 unsaturated synthetic resin Substances 0.000 description 1
- LSGOVYNHVSXFFJ-UHFFFAOYSA-N vanadate(3-) Chemical compound [O-][V]([O-])([O-])=O LSGOVYNHVSXFFJ-UHFFFAOYSA-N 0.000 description 1
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 1
- 239000004034 viscosity adjusting agent Substances 0.000 description 1
- 229910052727 yttrium Inorganic materials 0.000 description 1
- 229910052984 zinc sulfide Inorganic materials 0.000 description 1
- DRDVZXDWVBGGMH-UHFFFAOYSA-N zinc;sulfide Chemical compound [S-2].[Zn+2] DRDVZXDWVBGGMH-UHFFFAOYSA-N 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09B—ORGANIC DYES OR CLOSELY-RELATED COMPOUNDS FOR PRODUCING DYES, e.g. PIGMENTS; MORDANTS; LAKES
- C09B67/00—Influencing the physical, e.g. the dyeing or printing properties of dyestuffs without chemical reactions, e.g. by treating with solvents grinding or grinding assistants, coating of pigments or dyes; Process features in the making of dyestuff preparations; Dyestuff preparations of a special physical nature, e.g. tablets, films
- C09B67/0033—Blends of pigments; Mixtured crystals; Solid solutions
- C09B67/0034—Mixtures of two or more pigments or dyes of the same type
Landscapes
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Paints Or Removers (AREA)
- Inks, Pencil-Leads, Or Crayons (AREA)
- Pigments, Carbon Blacks, Or Wood Stains (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE102005024722A DE102005024722A1 (de) | 2005-05-31 | 2005-05-31 | Blaues Farbmittel auf Basis von C.I. Pigment Blue 80 |
| DE102005024722.9 | 2005-05-31 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| KR20080012322A true KR20080012322A (ko) | 2008-02-11 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| KR1020077027832A Withdrawn KR20080012322A (ko) | 2005-05-31 | 2006-04-29 | Ｃ.ｉ. 피그먼트 블루-80 계 청색 염료 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7686883B2 (https=) |
| EP (1) | EP1891163B1 (https=) |
| JP (1) | JP2008542482A (https=) |
| KR (1) | KR20080012322A (https=) |
| CN (1) | CN101208393A (https=) |
| BR (1) | BRPI0611212A2 (https=) |
| CA (1) | CA2610174A1 (https=) |
| DE (2) | DE102005024722A1 (https=) |
| ES (1) | ES2321978T3 (https=) |
| WO (1) | WO2006128539A2 (https=) |
Families Citing this family (11)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102006008308A1 (de) * | 2006-02-23 | 2007-08-30 | Clariant International Limited | Polysilazane enthaltende Beschichtungen zur Vermeidung von Zunderbildung und Korrosion |
| KR101482969B1 (ko) * | 2007-03-15 | 2015-01-21 | 신닛테츠 수미킨 가가쿠 가부시키가이샤 | 차광성 조성물 및 컬러필터 |
| DE102007031354A1 (de) | 2007-07-05 | 2009-01-08 | Clariant International Limited | Pigmentzubereitungen auf Basis von Dioxazinen |
| KR101069411B1 (ko) * | 2009-11-24 | 2011-10-04 | 삼성전기주식회사 | 휴대폰 |
| EP2565210B1 (en) * | 2010-04-28 | 2019-11-06 | Mitsui Chemicals, Inc. | Resin fine powder consisting of 4-methyl-1-pentene polymer, composition containing same, and process for production thereof |
| US9291873B2 (en) | 2011-06-10 | 2016-03-22 | Hewlett-Packard Development Company, L.P. | Surfactants with a terminal dialkyl- or cycloalkyl-substituted tertiary amine and inks including the same |
| WO2015136814A1 (ja) * | 2014-03-10 | 2015-09-17 | Dic株式会社 | 遮光性顔料組成物及びディスプレイ用遮光性部材 |
| JP6894953B2 (ja) * | 2014-11-04 | 2021-06-30 | クラリアント・インターナシヨナル・リミテツド | Ｃ．ｉ．ピグメントイエロー１５５とその製造方法、その顔料を用いた顔料組成物と着色剤組成物、及びそれらの着色剤としての使用 |
| US11542199B2 (en) | 2016-07-06 | 2023-01-03 | Huntsman Petrochemical Llc | Halogen-free quaternary amines and uses thereof |
| US20210230447A1 (en) * | 2018-05-03 | 2021-07-29 | Akzo Nobel Coatings International B.V. | Two-component coating composition, method for homogeneously mixing a curing component into a binder component, and use of nano pigments for providing a marker color to a curing component |
| EP4013822A1 (de) | 2019-08-12 | 2022-06-22 | BASF Coatings GmbH | Verfahren zur herstellung von effektpigmentpasten unter verwendung eines rüttlers |
Family Cites Families (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3838814A1 (de) * | 1987-12-22 | 1989-07-06 | Hoechst Ag | Neue pigmente und ihre verwendung |
| JP3388591B2 (ja) | 1991-03-22 | 2003-03-24 | クラリアント・ゲゼルシヤフト・ミト・ベシユレンクテル・ハフツング | Ｃ．ｉ．ピグメント・バイオレット２３を基礎とする顔料調製物の製造方法 |
| FR2713234B1 (fr) | 1993-12-06 | 1996-03-22 | Sandoz Sa | Nouveaux dérivés de la triphénodioxazine, leur préparation et leur utilisation comme pigments. |
| DE4442291B4 (de) * | 1993-12-06 | 2006-04-13 | Clariant Finance (Bvi) Ltd. | Triphendioxazin-Verbindungen |
| DE19747175A1 (de) * | 1997-10-24 | 1999-04-29 | Clariant Int Ltd | Chlorhaltige Triphendioxazin-Verbindungen |
| DE19800273A1 (de) * | 1998-01-07 | 1999-07-08 | Clariant Gmbh | Verfahren zur Herstellung von Bisoxazin-Verbindungen |
| US6375732B1 (en) * | 1999-04-08 | 2002-04-23 | Clariant Finance (Bvi) Limited | Pigments, the process of their manufacturing and their use |
| JP4526650B2 (ja) * | 1999-04-22 | 2010-08-18 | クラリアント ファイナンス （ビーブイアイ） リミティド | 固溶体 |
| DE10052221A1 (de) * | 2000-10-21 | 2002-05-02 | Clariant Gmbh | Verfahren zur Herstellung neuer Kristallmodifikationen eines methylsubstituierten Benzimidazolon-Dioxazin-Pigmentes |
| DE10052858A1 (de) * | 2000-10-24 | 2002-04-25 | Clariant Gmbh | Mischkristalle aus Benzimidazolondioxazin-Verbindungen |
| US6476222B2 (en) * | 2001-01-05 | 2002-11-05 | Sun Chemical Corporation | Preparation of heat stable pigment violet 23 |
| DE10256416A1 (de) | 2002-12-02 | 2004-06-09 | Basf Ag | Feste Pigmentzubereitungen, enthaltend Pigmentderivate und oberflächenaktive Additive |
| JP2005049636A (ja) * | 2003-07-29 | 2005-02-24 | Toyo Ink Mfg Co Ltd | カラーフィルタ用着色組成物およびカラーフィルタ |
| DE102004010284A1 (de) * | 2004-03-03 | 2005-09-22 | Clariant Gmbh | Pigmentzubereitungen auf Basis Phthalocyaninpigment |
| DE102004010282A1 (de) * | 2004-03-03 | 2005-09-22 | Clariant Gmbh | Violettes Farbmittel für Color Filter, Ink Jet Tinten, elektrophotographische Toner und Entwickler und e-inks |
-
2005
- 2005-05-31 DE DE102005024722A patent/DE102005024722A1/de not_active Withdrawn
-
2006
- 2006-04-29 KR KR1020077027832A patent/KR20080012322A/ko not_active Withdrawn
- 2006-04-29 BR BRPI0611212-9A patent/BRPI0611212A2/pt not_active IP Right Cessation
- 2006-04-29 JP JP2008513956A patent/JP2008542482A/ja not_active Ceased
- 2006-04-29 DE DE502006003329T patent/DE502006003329D1/de not_active Expired - Lifetime
- 2006-04-29 EP EP06753464A patent/EP1891163B1/de not_active Expired - Lifetime
- 2006-04-29 CN CNA2006800228863A patent/CN101208393A/zh active Pending
- 2006-04-29 WO PCT/EP2006/004055 patent/WO2006128539A2/de not_active Ceased
- 2006-04-29 ES ES06753464T patent/ES2321978T3/es not_active Expired - Lifetime
- 2006-04-29 CA CA002610174A patent/CA2610174A1/en not_active Abandoned
- 2006-04-29 US US11/921,550 patent/US7686883B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| EP1891163A2 (de) | 2008-02-27 |
| BRPI0611212A2 (pt) | 2010-08-24 |
| JP2008542482A (ja) | 2008-11-27 |
| CN101208393A (zh) | 2008-06-25 |
| WO2006128539A3 (de) | 2007-02-01 |
| EP1891163B1 (de) | 2009-04-01 |
| US20090121202A1 (en) | 2009-05-14 |
| WO2006128539A2 (de) | 2006-12-07 |
| DE502006003329D1 (de) | 2009-05-14 |
| US7686883B2 (en) | 2010-03-30 |
| ES2321978T3 (es) | 2009-06-15 |
| CA2610174A1 (en) | 2006-12-07 |
| DE102005024722A1 (de) | 2006-12-07 |
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Legal Events
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| PA0105 | International application |
Patent event date: 20071129 Patent event code: PA01051R01D Comment text: International Patent Application |
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| PG1501 | Laying open of application | ||
| PC1203 | Withdrawal of no request for examination | ||
| WITN | Application deemed withdrawn, e.g. because no request for examination was filed or no examination fee was paid |