ES2619169T3 - Composiciones cosméticas que contienen ésteres a base de 2-propilheptanol - Google Patents
Composiciones cosméticas que contienen ésteres a base de 2-propilheptanol Download PDFInfo
- Publication number
- ES2619169T3 ES2619169T3 ES08748951.4T ES08748951T ES2619169T3 ES 2619169 T3 ES2619169 T3 ES 2619169T3 ES 08748951 T ES08748951 T ES 08748951T ES 2619169 T3 ES2619169 T3 ES 2619169T3
- Authority
- ES
- Spain
- Prior art keywords
- acid
- propylheptyl
- ester
- esters
- weight
- 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.)
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- 150000002148 esters Chemical class 0.000 title claims abstract description 83
- YLQLIQIAXYRMDL-UHFFFAOYSA-N propylheptyl alcohol Chemical compound CCCCCC(CO)CCC YLQLIQIAXYRMDL-UHFFFAOYSA-N 0.000 title claims abstract description 23
- 239000000203 mixture Substances 0.000 title claims description 67
- 239000002537 cosmetic Substances 0.000 title claims description 23
- -1 2-propylheptyl-1,4-benzenedicarboxylic acid ester Chemical class 0.000 claims abstract description 88
- 150000001558 benzoic acid derivatives Chemical class 0.000 claims abstract description 21
- 150000005690 diesters Chemical class 0.000 claims abstract description 20
- QBYDDGFDWXCFIH-UHFFFAOYSA-N 3,4-bis(2-propylheptyl)phthalic acid Chemical compound CCCCCC(CCC)CC1=CC=C(C(O)=O)C(C(O)=O)=C1CC(CCC)CCCCC QBYDDGFDWXCFIH-UHFFFAOYSA-N 0.000 claims abstract description 6
- RFDCPLOGAXUARH-UHFFFAOYSA-N C(CC)C(CCC(=O)OC=1C(C(=O)O)=CC=CC=1)CCCCC Chemical compound C(CC)C(CCC(=O)OC=1C(C(=O)O)=CC=CC=1)CCCCC RFDCPLOGAXUARH-UHFFFAOYSA-N 0.000 claims abstract description 5
- IZLZYIVYIKPENA-UHFFFAOYSA-N 2,3-bis(2-propylheptyl)terephthalic acid Chemical compound CCCCCC(CCC)CC1=C(CC(CCC)CCCCC)C(C(O)=O)=CC=C1C(O)=O IZLZYIVYIKPENA-UHFFFAOYSA-N 0.000 claims abstract 2
- 239000002253 acid Substances 0.000 claims description 34
- 239000003995 emulsifying agent Substances 0.000 claims description 33
- 229920000642 polymer Polymers 0.000 claims description 16
- 239000004094 surface-active agent Substances 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 12
- GPSDUZXPYCFOSQ-UHFFFAOYSA-N m-toluenecarboxylic acid Natural products CC1=CC=CC(C(O)=O)=C1 GPSDUZXPYCFOSQ-UHFFFAOYSA-N 0.000 claims description 5
- FGELLQLLAUDCBF-UHFFFAOYSA-N 2-acetyloxy-3-(2-propylheptyl)benzoic acid Chemical compound C(CC)C(CC=1C(=C(C(=O)O)C=CC=1)OC(C)=O)CCCCC FGELLQLLAUDCBF-UHFFFAOYSA-N 0.000 claims description 3
- 239000008194 pharmaceutical composition Substances 0.000 claims description 2
- 239000001993 wax Substances 0.000 description 47
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 36
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 34
- 239000000194 fatty acid Substances 0.000 description 33
- 235000014113 dietary fatty acids Nutrition 0.000 description 32
- 229930195729 fatty acid Natural products 0.000 description 32
- 125000000217 alkyl group Chemical group 0.000 description 31
- 239000000047 product Substances 0.000 description 31
- 235000010233 benzoic acid Nutrition 0.000 description 30
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- 235000019441 ethanol Nutrition 0.000 description 26
- 238000002360 preparation method Methods 0.000 description 24
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- 150000001559 benzoic acids Chemical group 0.000 description 22
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 21
- 150000002191 fatty alcohols Chemical class 0.000 description 20
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 17
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- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 10
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- 230000032050 esterification Effects 0.000 description 9
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- ULQISTXYYBZJSJ-UHFFFAOYSA-N 12-hydroxyoctadecanoic acid Chemical compound CCCCCCC(O)CCCCCCCCCCC(O)=O ULQISTXYYBZJSJ-UHFFFAOYSA-N 0.000 description 8
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- 125000004429 atom Chemical group 0.000 description 8
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- WXBLLCUINBKULX-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1.OC(=O)C1=CC=CC=C1 WXBLLCUINBKULX-UHFFFAOYSA-N 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 7
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical class OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 7
- 150000003839 salts Chemical class 0.000 description 7
- 150000003626 triacylglycerols Chemical class 0.000 description 7
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 6
- 125000002091 cationic group Chemical group 0.000 description 6
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- 239000002904 solvent Substances 0.000 description 6
- 238000005809 transesterification reaction Methods 0.000 description 6
- IOHPVZBSOKLVMN-UHFFFAOYSA-N 2-(2-phenylethyl)benzoic acid Chemical compound OC(=O)C1=CC=CC=C1CCC1=CC=CC=C1 IOHPVZBSOKLVMN-UHFFFAOYSA-N 0.000 description 5
- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 5
- 125000002252 acyl group Chemical group 0.000 description 5
- 230000010933 acylation Effects 0.000 description 5
- 238000005917 acylation reaction Methods 0.000 description 5
- 230000001166 anti-perspirative effect Effects 0.000 description 5
- 239000003213 antiperspirant Substances 0.000 description 5
- 150000002170 ethers Chemical class 0.000 description 5
- 239000000077 insect repellent Substances 0.000 description 5
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 5
- 239000000787 lecithin Substances 0.000 description 5
- 235000010445 lecithin Nutrition 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- 230000001953 sensory effect Effects 0.000 description 5
- 235000019484 Rapeseed oil Nutrition 0.000 description 4
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- 239000003945 anionic surfactant Substances 0.000 description 4
- 238000009826 distribution Methods 0.000 description 4
- UKMSUNONTOPOIO-UHFFFAOYSA-N docosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCCCCC(O)=O UKMSUNONTOPOIO-UHFFFAOYSA-N 0.000 description 4
- 239000010696 ester oil Substances 0.000 description 4
- 238000002844 melting Methods 0.000 description 4
- 230000008018 melting Effects 0.000 description 4
- 150000004702 methyl esters Chemical class 0.000 description 4
- ZWLPBLYKEWSWPD-UHFFFAOYSA-N o-toluic acid Chemical class CC1=CC=CC=C1C(O)=O ZWLPBLYKEWSWPD-UHFFFAOYSA-N 0.000 description 4
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 4
- LPNBBFKOUUSUDB-UHFFFAOYSA-N p-toluic acid Chemical compound CC1=CC=C(C(O)=O)C=C1 LPNBBFKOUUSUDB-UHFFFAOYSA-N 0.000 description 4
- HLZKNKRTKFSKGZ-UHFFFAOYSA-N tetradecan-1-ol Chemical compound CCCCCCCCCCCCCCO HLZKNKRTKFSKGZ-UHFFFAOYSA-N 0.000 description 4
- AFDXODALSZRGIH-QPJJXVBHSA-N (E)-3-(4-methoxyphenyl)prop-2-enoic acid Chemical compound COC1=CC=C(\C=C\C(O)=O)C=C1 AFDXODALSZRGIH-QPJJXVBHSA-N 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 3
- 229940114072 12-hydroxystearic acid Drugs 0.000 description 3
- KIHBGTRZFAVZRV-UHFFFAOYSA-N 2-hydroxyoctadecanoic acid Chemical compound CCCCCCCCCCCCCCCCC(O)C(O)=O KIHBGTRZFAVZRV-UHFFFAOYSA-N 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
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- 235000013162 Cocos nucifera Nutrition 0.000 description 3
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- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 3
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
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- UJMDYLWCYJJYMO-UHFFFAOYSA-N benzene-1,2,3-tricarboxylic acid Chemical class OC(=O)C1=CC=CC(C(O)=O)=C1C(O)=O UJMDYLWCYJJYMO-UHFFFAOYSA-N 0.000 description 3
- KKEYFWRCBNTPAC-UHFFFAOYSA-N benzene-dicarboxylic acid Natural products OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 3
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- GOQYKNQRPGWPLP-UHFFFAOYSA-N heptadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 3
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- 229920001897 terpolymer Polymers 0.000 description 1
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- HBPNTDBLHQHPLH-UHFFFAOYSA-N tetradecyl 16-methylheptadecanoate Chemical compound CCCCCCCCCCCCCCOC(=O)CCCCCCCCCCCCCCC(C)C HBPNTDBLHQHPLH-UHFFFAOYSA-N 0.000 description 1
- AVKVDDQTHIQFSC-UHFFFAOYSA-N tetradecyl docosanoate Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC AVKVDDQTHIQFSC-UHFFFAOYSA-N 0.000 description 1
- DHZWALZKPWZSMA-UHFFFAOYSA-N tetradecyl oleate Natural products CCCCCCCCCCCCCCOC(=O)CCCCCCCC=CCCCCCCCC DHZWALZKPWZSMA-UHFFFAOYSA-N 0.000 description 1
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- 230000001960 triggered effect Effects 0.000 description 1
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
- OUYCCCASQSFEME-UHFFFAOYSA-N tyrosine Natural products OC(=O)C(N)CC1=CC=C(O)C=C1 OUYCCCASQSFEME-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/37—Esters of carboxylic acids
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/16—Emollients or protectives, e.g. against radiation
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Dermatology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Medicinal Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Emergency Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Toxicology (AREA)
- Cosmetics (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07008475 | 2007-04-26 | ||
| EP07008475A EP1985279A1 (de) | 2007-04-26 | 2007-04-26 | Kosmetische Zusammensetzungen enthaltend Ester auf Basis von 2-Propylheptanol |
| PCT/EP2008/003066 WO2008131862A2 (de) | 2007-04-26 | 2008-04-17 | Kosmetische zusammensetzungen enthaltend ester auf basis von 2- propylheptanol |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2619169T3 true ES2619169T3 (es) | 2017-06-23 |
Family
ID=38477281
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES08748951.4T Active ES2619169T3 (es) | 2007-04-26 | 2008-04-17 | Composiciones cosméticas que contienen ésteres a base de 2-propilheptanol |
Country Status (7)
| Country | Link |
|---|---|
| US (3) | US8288436B2 (enExample) |
| EP (2) | EP1985279A1 (enExample) |
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| CN (1) | CN101668507A (enExample) |
| ES (1) | ES2619169T3 (enExample) |
| WO (1) | WO2008131862A2 (enExample) |
Families Citing this family (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102011077365A1 (de) * | 2011-06-10 | 2012-12-13 | Henkel Ag & Co. Kgaa | Stylingmittel mit interessanter Textur |
| US10496797B2 (en) * | 2012-08-30 | 2019-12-03 | Medtronic Minimed, Inc. | Blood glucose validation for a closed-loop operating mode of an insulin infusion system |
| US9085670B2 (en) | 2012-10-10 | 2015-07-21 | Lg Chem, Ltd. | Plasticizer, plasticizer composition, heat-resistant resin composition and method for preparing the same |
| CN103975010B (zh) * | 2012-10-10 | 2016-04-20 | Lg化学株式会社 | 增塑剂、增塑剂组合物、耐热树脂组合物及其制备方法 |
| GB201406257D0 (en) * | 2014-04-07 | 2014-05-21 | Univ City | System & method for estimating substance concentrations in bodily fluids |
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|---|---|---|---|---|
| US2921089A (en) * | 1957-11-27 | 1960-01-12 | Eastman Kodak Co | 2-propylheptanol and its esters |
| JPS58206537A (ja) * | 1982-05-14 | 1983-12-01 | モンサント・カンパニ− | ２−プロピルヘプタノ−ルおよびその他のアルコ−ルの製造法 |
| JP2773290B2 (ja) * | 1988-10-25 | 1998-07-09 | 三菱化学株式会社 | 可塑剤及び可塑剤用アルコール |
| JPH06166644A (ja) * | 1992-12-01 | 1994-06-14 | Chisso Corp | 可塑剤用混合アルコール及びそれを用いた可塑剤 |
| JPH05214159A (ja) * | 1992-02-04 | 1993-08-24 | Chisso Corp | 可塑剤用混合アルコール及びそれを用いた可塑剤 |
| JPH0616889A (ja) * | 1992-07-01 | 1994-01-25 | Sekisui Chem Co Ltd | 塩化ビニル系樹脂組成物及びそれを用いたガラス・塩化ビニル系樹脂一体成形体 |
| WO1994010131A1 (en) * | 1992-11-03 | 1994-05-11 | Unilever Plc | Method of synthesising phytosphingosine-containing ceramides and cosmetic compositions comprising them |
| FR2718022B1 (fr) * | 1994-04-01 | 1996-04-26 | Roussel Uclaf | Compositions cosmétiques ou dermatologiques et leur préparation. |
| DE4420516C2 (de) | 1994-06-13 | 1998-10-22 | Henkel Kgaa | Polyglycerinpolyhydroxystearate |
| JPH083537A (ja) * | 1994-06-23 | 1996-01-09 | Sekisui Chem Co Ltd | シーリング材組成物 |
| JPH08245847A (ja) * | 1995-03-13 | 1996-09-24 | Mitsubishi Chem Mkv Co | 塩素化ポリエチレン樹脂組成物 |
| JPH08301295A (ja) * | 1995-04-28 | 1996-11-19 | Mitsubishi Chem Corp | フレキシブルコンテナ |
| US6355711B1 (en) * | 1998-04-23 | 2002-03-12 | Exxonmobil Chemical Patents Inc. | High performance plasticizers from branched oxo alcohols |
| DE10160681A1 (de) | 2001-12-11 | 2003-06-18 | Cognis Deutschland Gmbh | Emollients und kosmetische Zusammensetzungen |
| DE10160682A1 (de) | 2001-12-11 | 2003-06-18 | Cognis Deutschland Gmbh | Emollients und kosmetische Zusammensetzungen |
| DE10249912A1 (de) | 2002-10-26 | 2004-05-06 | Oxeno Olefinchemie Gmbh | Benzoesäureisodecyclestergemische, Herstellung und deren Verwendung |
| DE10305562A1 (de) | 2003-02-10 | 2004-08-26 | Sasol Germany Gmbh | Estermischungen auf Basis verzweigter Alkohole und/oder verzweigter Säuren und deren Verwendung als Polymeradditiv |
| DE10317781A1 (de) * | 2003-04-16 | 2004-11-04 | Cognis Deutschland Gmbh & Co. Kg | Poly-alpha-Olefin-haltige kosmetische Zusammensetzung |
| JP4391293B2 (ja) * | 2004-04-01 | 2009-12-24 | 株式会社資生堂 | 紫外線吸収剤及びこれを含有する皮膚外用剤 |
| EP1858480B3 (de) | 2005-03-17 | 2020-05-06 | Cognis IP Management GmbH | Kosmetische zusammensetzungen enthaltend ester auf basis von 2- propylheptanol |
-
2007
- 2007-04-26 EP EP07008475A patent/EP1985279A1/de not_active Withdrawn
-
2008
- 2008-04-17 CN CN200880013333A patent/CN101668507A/zh active Pending
- 2008-04-17 EP EP08748951.4A patent/EP2136767B1/de active Active
- 2008-04-17 JP JP2010504506A patent/JP5666900B2/ja active Active
- 2008-04-17 US US12/597,577 patent/US8288436B2/en active Active
- 2008-04-17 KR KR1020097022242A patent/KR101568429B1/ko active Active
- 2008-04-17 WO PCT/EP2008/003066 patent/WO2008131862A2/de not_active Ceased
- 2008-04-17 ES ES08748951.4T patent/ES2619169T3/es active Active
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2012
- 2012-09-12 US US13/611,388 patent/US8633333B2/en active Active
- 2012-09-12 US US13/611,344 patent/US8633244B2/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| WO2008131862A2 (de) | 2008-11-06 |
| JP5666900B2 (ja) | 2015-02-12 |
| US8633244B2 (en) | 2014-01-21 |
| US20130004555A1 (en) | 2013-01-03 |
| EP2136767B1 (de) | 2016-12-14 |
| JP2010526772A (ja) | 2010-08-05 |
| WO2008131862A3 (de) | 2009-03-26 |
| KR101568429B1 (ko) | 2015-11-11 |
| US20130006010A1 (en) | 2013-01-03 |
| US8288436B2 (en) | 2012-10-16 |
| EP2136767A2 (de) | 2009-12-30 |
| US8633333B2 (en) | 2014-01-21 |
| CN101668507A (zh) | 2010-03-10 |
| KR20100015866A (ko) | 2010-02-12 |
| US20100120910A1 (en) | 2010-05-13 |
| EP1985279A1 (de) | 2008-10-29 |
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