JP2011502107A5 - - Google Patents
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- JP2011502107A5 JP2011502107A5 JP2010528356A JP2010528356A JP2011502107A5 JP 2011502107 A5 JP2011502107 A5 JP 2011502107A5 JP 2010528356 A JP2010528356 A JP 2010528356A JP 2010528356 A JP2010528356 A JP 2010528356A JP 2011502107 A5 JP2011502107 A5 JP 2011502107A5
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- JP
- Japan
- Prior art keywords
- composition
- compounds
- hydroxy
- component
- present
- 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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- 239000000203 mixture Substances 0.000 claims description 126
- 239000000047 product Substances 0.000 claims description 72
- -1 polysiloxane Polymers 0.000 claims description 56
- 150000001875 compounds Chemical class 0.000 claims description 49
- 239000004744 fabric Substances 0.000 claims description 36
- 239000000835 fiber Substances 0.000 claims description 28
- 125000000217 alkyl group Chemical group 0.000 claims description 25
- 239000003381 stabilizer Substances 0.000 claims description 22
- 238000000034 method Methods 0.000 claims description 16
- 238000004140 cleaning Methods 0.000 claims description 14
- 230000000087 stabilizing effect Effects 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 12
- 239000010985 leather Substances 0.000 claims description 11
- 239000000843 powder Substances 0.000 claims description 11
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- 239000002979 fabric softener Substances 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 125000003884 phenylalkyl group Chemical group 0.000 claims description 8
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 239000004611 light stabiliser Substances 0.000 claims description 7
- 239000000049 pigment Substances 0.000 claims description 7
- 239000007921 spray Substances 0.000 claims description 7
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 6
- 239000007844 bleaching agent Substances 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
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- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- GHKOFFNLGXMVNJ-UHFFFAOYSA-N Didodecyl thiobispropanoate Chemical compound CCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCC GHKOFFNLGXMVNJ-UHFFFAOYSA-N 0.000 claims description 5
- 239000003508 Dilauryl thiodipropionate Substances 0.000 claims description 5
- 239000002656 Distearyl thiodipropionate Substances 0.000 claims description 5
- 235000019304 dilauryl thiodipropionate Nutrition 0.000 claims description 5
- PWWSSIYVTQUJQQ-UHFFFAOYSA-N distearyl thiodipropionate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSCCC(=O)OCCCCCCCCCCCCCCCCCC PWWSSIYVTQUJQQ-UHFFFAOYSA-N 0.000 claims description 5
- 235000019305 distearyl thiodipropionate Nutrition 0.000 claims description 5
- 229920002554 vinyl polymer Polymers 0.000 claims description 5
- 239000002253 acid Substances 0.000 claims description 4
- 239000003513 alkali Substances 0.000 claims description 4
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 claims description 4
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- 238000005498 polishing Methods 0.000 claims description 4
- 150000003839 salts Chemical class 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 3
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 claims description 3
- 229910052751 metal Inorganic materials 0.000 claims description 3
- 239000002184 metal Substances 0.000 claims description 3
- 239000006097 ultraviolet radiation absorber Substances 0.000 claims description 3
- JIHQDMXYYFUGFV-UHFFFAOYSA-N 1,3,5-triazine Chemical compound C1=NC=NC=N1 JIHQDMXYYFUGFV-UHFFFAOYSA-N 0.000 claims description 2
- IJVRPNIWWODHHA-UHFFFAOYSA-N 2-cyanoprop-2-enoic acid Chemical compound OC(=O)C(=C)C#N IJVRPNIWWODHHA-UHFFFAOYSA-N 0.000 claims description 2
- 239000005711 Benzoic acid Substances 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 230000002378 acidificating effect Effects 0.000 claims description 2
- 125000004414 alkyl thio group Chemical group 0.000 claims description 2
- 235000010233 benzoic acid Nutrition 0.000 claims description 2
- RWCCWEUUXYIKHB-UHFFFAOYSA-N benzophenone Chemical compound C=1C=CC=CC=1C(=O)C1=CC=CC=C1 RWCCWEUUXYIKHB-UHFFFAOYSA-N 0.000 claims description 2
- 239000012965 benzophenone Substances 0.000 claims description 2
- QRUDEWIWKLJBPS-UHFFFAOYSA-N benzotriazole Chemical compound C1=CC=C2N[N][N]C2=C1 QRUDEWIWKLJBPS-UHFFFAOYSA-N 0.000 claims description 2
- 239000000919 ceramic Substances 0.000 claims description 2
- OHCIBJNNZNPROG-UHFFFAOYSA-N dilauryl 3,3'-thiodipropionate Chemical compound CCCCCCCCCCCCOC(=O)CCSSCCC(=O)OCCCCCCCCCCCC OHCIBJNNZNPROG-UHFFFAOYSA-N 0.000 claims description 2
- 238000004851 dishwashing Methods 0.000 claims description 2
- 230000000694 effects Effects 0.000 claims description 2
- 230000009931 harmful effect Effects 0.000 claims description 2
- FTWUXYZHDFCGSV-UHFFFAOYSA-N n,n'-diphenyloxamide Chemical compound C=1C=CC=CC=1NC(=O)C(=O)NC1=CC=CC=C1 FTWUXYZHDFCGSV-UHFFFAOYSA-N 0.000 claims description 2
- 230000007935 neutral effect Effects 0.000 claims description 2
- XPNWIWHUGHAVLC-UHFFFAOYSA-N octadecyl 3-[(3-octadecoxy-3-oxopropyl)disulfanyl]propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCSSCCC(=O)OCCCCCCCCCCCCCCCCCC XPNWIWHUGHAVLC-UHFFFAOYSA-N 0.000 claims description 2
- 230000003287 optical effect Effects 0.000 claims description 2
- 229920001296 polysiloxane Polymers 0.000 claims description 2
- 238000009991 scouring Methods 0.000 claims description 2
- 230000002939 deleterious effect Effects 0.000 claims 3
- 150000002431 hydrogen Chemical class 0.000 claims 2
- 230000002411 adverse Effects 0.000 claims 1
- 239000003086 colorant Substances 0.000 claims 1
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- 239000000975 dye Substances 0.000 description 27
- 238000002360 preparation method Methods 0.000 description 21
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 14
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- 125000004432 carbon atom Chemical group C* 0.000 description 12
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- 239000000194 fatty acid Substances 0.000 description 11
- 229930195729 fatty acid Natural products 0.000 description 11
- 239000012071 phase Substances 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 11
- 229920000742 Cotton Polymers 0.000 description 10
- 239000000463 material Substances 0.000 description 10
- 239000003921 oil Substances 0.000 description 10
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 235000006708 antioxidants Nutrition 0.000 description 9
- 125000003118 aryl group Chemical group 0.000 description 9
- 238000002845 discoloration Methods 0.000 description 8
- 229910052757 nitrogen Inorganic materials 0.000 description 8
- 238000003756 stirring Methods 0.000 description 8
- 238000011282 treatment Methods 0.000 description 8
- 125000003342 alkenyl group Chemical group 0.000 description 7
- 239000003995 emulsifying agent Substances 0.000 description 7
- 239000006210 lotion Substances 0.000 description 7
- BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 7
- QPCDCPDFJACHGM-UHFFFAOYSA-N N,N-bis{2-[bis(carboxymethyl)amino]ethyl}glycine Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(=O)O)CCN(CC(O)=O)CC(O)=O QPCDCPDFJACHGM-UHFFFAOYSA-N 0.000 description 6
- 238000004043 dyeing Methods 0.000 description 6
- 230000000996 additive effect Effects 0.000 description 5
- 239000002537 cosmetic Substances 0.000 description 5
- 150000002430 hydrocarbons Chemical class 0.000 description 5
- 239000002674 ointment Substances 0.000 description 5
- 238000003860 storage Methods 0.000 description 5
- 239000001993 wax Substances 0.000 description 5
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- UQSXHKLRYXJYBZ-UHFFFAOYSA-N Iron oxide Chemical compound [Fe]=O UQSXHKLRYXJYBZ-UHFFFAOYSA-N 0.000 description 4
- 239000004480 active ingredient Substances 0.000 description 4
- 229960000541 cetyl alcohol Drugs 0.000 description 4
- 230000008021 deposition Effects 0.000 description 4
- 150000002191 fatty alcohols Chemical class 0.000 description 4
- 230000003020 moisturizing effect Effects 0.000 description 4
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 4
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N phenol group Chemical group C1(=CC=CC=C1)O ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 4
- 239000002530 phenolic antioxidant Substances 0.000 description 4
- XTXADMXOEMEPAC-UHFFFAOYSA-M sodium;3-(benzotriazol-2-yl)-5-butan-2-yl-4-hydroxybenzenesulfonate Chemical compound [Na+].CCC(C)C1=CC(S([O-])(=O)=O)=CC(N2N=C3C=CC=CC3=N2)=C1O XTXADMXOEMEPAC-UHFFFAOYSA-M 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- FYQOHJWNKFULEZ-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CC(C)(O)CON1C(C)(C)CC(O)CC1(C)C FYQOHJWNKFULEZ-UHFFFAOYSA-N 0.000 description 3
- FUVBNYKKKZSBCG-UHFFFAOYSA-N 1-(2-hydroxy-2-methylpropoxy)-2,2,6,6-tetramethylpiperidin-4-one Chemical compound CC(C)(O)CON1C(C)(C)CC(=O)CC1(C)C FUVBNYKKKZSBCG-UHFFFAOYSA-N 0.000 description 3
- ZXDDPOHVAMWLBH-UHFFFAOYSA-N 2,4-Dihydroxybenzophenone Chemical compound OC1=CC(O)=CC=C1C(=O)C1=CC=CC=C1 ZXDDPOHVAMWLBH-UHFFFAOYSA-N 0.000 description 3
- RXFCIXRFAJRBSG-UHFFFAOYSA-N 3,2,3-tetramine Chemical compound NCCCNCCNCCCN RXFCIXRFAJRBSG-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 241000196324 Embryophyta Species 0.000 description 3
- 229920001214 Polysorbate 60 Polymers 0.000 description 3
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 3
- 239000003082 abrasive agent Substances 0.000 description 3
- 125000001931 aliphatic group Chemical group 0.000 description 3
- 125000000129 anionic group Chemical group 0.000 description 3
- 230000003078 antioxidant effect Effects 0.000 description 3
- 125000001589 carboacyl group Chemical group 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 125000000392 cycloalkenyl group Chemical group 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
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- 239000008240 homogeneous mixture Substances 0.000 description 3
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- 125000004435 hydrogen atom Chemical class [H]* 0.000 description 3
- 229910044991 metal oxide Inorganic materials 0.000 description 3
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- VKZRWSNIWNFCIQ-WDSKDSINSA-N (2s)-2-[2-[[(1s)-1,2-dicarboxyethyl]amino]ethylamino]butanedioic acid Chemical compound OC(=O)C[C@@H](C(O)=O)NCCN[C@H](C(O)=O)CC(O)=O VKZRWSNIWNFCIQ-WDSKDSINSA-N 0.000 description 2
- JOIILICURMPDPO-UHFFFAOYSA-N 1-methoxy-2,2,6,6-tetramethyl-4-propoxypiperidin-1-ium;oxalate Chemical compound [O-]C(=O)C([O-])=O.CCCOC1CC(C)(C)[NH+](OC)C(C)(C)C1.CCCOC1CC(C)(C)[NH+](OC)C(C)(C)C1 JOIILICURMPDPO-UHFFFAOYSA-N 0.000 description 2
- NYNSFQBRQGSYKP-UHFFFAOYSA-N 1-methoxy-2,2,6,6-tetramethylpiperidin-4-ol Chemical compound CON1C(C)(C)CC(O)CC1(C)C NYNSFQBRQGSYKP-UHFFFAOYSA-N 0.000 description 2
- BWJKLDGAAPQXGO-UHFFFAOYSA-N 2,2,6,6-tetramethyl-4-octadecoxypiperidine Chemical compound CCCCCCCCCCCCCCCCCCOC1CC(C)(C)NC(C)(C)C1 BWJKLDGAAPQXGO-UHFFFAOYSA-N 0.000 description 2
- BYEXEDGQQCKLQD-UHFFFAOYSA-N 2,2-ditert-butyl-3-(4-hydroxyphenyl)henicosanoic acid Chemical compound CCCCCCCCCCCCCCCCCCC(C(C(O)=O)(C(C)(C)C)C(C)(C)C)C1=CC=C(O)C=C1 BYEXEDGQQCKLQD-UHFFFAOYSA-N 0.000 description 2
- ZMWRRFHBXARRRT-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-4,6-bis(2-methylbutan-2-yl)phenol Chemical compound CCC(C)(C)C1=CC(C(C)(C)CC)=CC(N2N=C3C=CC=CC3=N2)=C1O ZMWRRFHBXARRRT-UHFFFAOYSA-N 0.000 description 2
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- UZUNCLSDTUBVCN-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-(2-phenylpropan-2-yl)-4-(2,4,4-trimethylpentan-2-yl)phenol Chemical compound C=1C(C(C)(C)CC(C)(C)C)=CC(N2N=C3C=CC=CC3=N2)=C(O)C=1C(C)(C)C1=CC=CC=C1 UZUNCLSDTUBVCN-UHFFFAOYSA-N 0.000 description 2
- VQMHSKWEJGIXGA-UHFFFAOYSA-N 2-(benzotriazol-2-yl)-6-dodecyl-4-methylphenol Chemical compound CCCCCCCCCCCCC1=CC(C)=CC(N2N=C3C=CC=CC3=N2)=C1O VQMHSKWEJGIXGA-UHFFFAOYSA-N 0.000 description 2
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- HIQIXEFWDLTDED-UHFFFAOYSA-N 4-hydroxy-1-piperidin-4-ylpyrrolidin-2-one Chemical compound O=C1CC(O)CN1C1CCNCC1 HIQIXEFWDLTDED-UHFFFAOYSA-N 0.000 description 2
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- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
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- VNWKTOKETHGBQD-UHFFFAOYSA-N methane Chemical compound C VNWKTOKETHGBQD-UHFFFAOYSA-N 0.000 description 2
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- MGFYIUFZLHCRTH-UHFFFAOYSA-N nitrilotriacetic acid Chemical compound OC(=O)CN(CC(O)=O)CC(O)=O MGFYIUFZLHCRTH-UHFFFAOYSA-N 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- ODUCDPQEXGNKDN-UHFFFAOYSA-N nitroxyl Chemical class O=N ODUCDPQEXGNKDN-UHFFFAOYSA-N 0.000 description 2
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- 125000000913 palmityl 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])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 2
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| PCT/EP2008/062987 WO2009047150A2 (en) | 2007-10-09 | 2008-09-29 | Body-care and household products and compositions comprising specific sulfur-containing compounds |
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| JP5732254B2 JP5732254B2 (ja) | 2015-06-10 |
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| JP2014214975A Active JP6097734B2 (ja) | 2007-10-09 | 2014-10-22 | 特定の硫黄含有化合物を含むボディケアおよび家庭用製品ならびに組成物 |
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| EP2166078B1 (en) * | 2008-09-12 | 2018-11-21 | The Procter & Gamble Company | Laundry particle made by extrusion comprising a hueing dye |
| DE102009028891A1 (de) * | 2009-08-26 | 2011-03-03 | Henkel Ag & Co. Kgaa | Verbesserte Waschleistung durch Radikalfänger |
| WO2011028567A2 (en) * | 2009-09-02 | 2011-03-10 | Access Business Group International Llc | Composition and method for skin repair |
| WO2014121074A1 (en) * | 2013-02-01 | 2014-08-07 | Fischer Beth | Aqueous cleanser for dental appliances |
| CN103421431A (zh) * | 2013-08-14 | 2013-12-04 | 吴江市利达上光制品有限公司 | 一种新型白鞋油及其制备方法 |
| TWI513762B (zh) * | 2014-04-09 | 2015-12-21 | Fdc Lees Chemical Industry Co | 雙官能型安定劑及其組成物 |
| WO2017172567A1 (en) | 2016-03-28 | 2017-10-05 | The Procter & Gamble Company | Long lasting and stable freshening compositions and methods of freshening the air |
| US11246816B2 (en) | 2016-06-30 | 2022-02-15 | The Procter And Gamble Company | Shampoo compositions comprising a chelant |
| US11786447B2 (en) | 2016-06-30 | 2023-10-17 | The Procter & Gamble Company | Conditioner composition comprising a chelant |
| US20180000705A1 (en) | 2016-06-30 | 2018-01-04 | The Procter & Gamble Company | Shampoo Compositions Comprising a Chelant |
| US20180000715A1 (en) | 2016-06-30 | 2018-01-04 | The Procter & Gamble Company | Hair Care Compositions For Calcium Chelation |
| US20180000706A1 (en) | 2016-06-30 | 2018-01-04 | The Procter & Gamble Company | Conditioner Composition Comprising a Chelant |
| CA3047424A1 (en) * | 2016-12-22 | 2018-06-28 | Unilever Plc | Stabilization of cosmetic compositions comprising fish oils and hydroxylated fatty acids and/or its derivatives |
| EA038222B1 (ru) * | 2016-12-22 | 2021-07-26 | ЮНИЛЕВЕР АйПи ХОЛДИНГС Б.В. | Композиция для ухода за кожей и ее применение |
| EP3613835A1 (en) | 2018-08-24 | 2020-02-26 | The Procter & Gamble Company | Treatment compositions comprising a surfactant system and an oligoamine |
| EP3613834B1 (en) | 2018-08-24 | 2026-04-01 | The Procter & Gamble Company | Treatment compositions comprising low levels of an oligoamine |
| EP3866753B1 (en) | 2018-10-15 | 2025-11-26 | Unilever IP Holdings B.V. | An antiperspirant composition |
| MX2022004661A (es) * | 2019-10-25 | 2022-05-25 | Unilever Ip Holdings B V | Composicion cosmetica con estabilidad de color mejorada. |
| WO2021128045A1 (en) * | 2019-12-25 | 2021-07-01 | L'oreal | Composition for conditioning keratain fibers |
| US11554087B2 (en) * | 2020-11-05 | 2023-01-17 | The Gillette Company Llc | Shaving aid comprising an antioxidant |
| FR3138033B1 (fr) * | 2022-07-21 | 2026-03-13 | Oreal | Composition parfumée comprenant au moins un composé antioxydant soufré, au moins un filtre UV organique et au moins une substance parfumante |
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| AU2008201924A1 (en) * | 2006-05-15 | 2008-05-22 | Wyeth | Stabilised formulation |
-
2008
- 2008-08-27 US US12/229,815 patent/US20090092561A1/en not_active Abandoned
- 2008-09-29 CN CN201510007412.2A patent/CN104586637A/zh active Pending
- 2008-09-29 MX MX2010003353A patent/MX345135B/es active IP Right Grant
- 2008-09-29 WO PCT/EP2008/062987 patent/WO2009047150A2/en not_active Ceased
- 2008-09-29 EP EP08804849.1A patent/EP2207522B1/en active Active
- 2008-09-29 KR KR1020167020215A patent/KR20160092050A/ko not_active Ceased
- 2008-09-29 JP JP2010528356A patent/JP5732254B2/ja active Active
- 2008-09-29 CN CN200880110917XA patent/CN102014856A/zh active Pending
- 2008-09-29 ES ES08804849T patent/ES2766255T3/es active Active
- 2008-09-29 KR KR1020107010105A patent/KR20100086997A/ko not_active Ceased
- 2008-09-29 PL PL08804849T patent/PL2207522T3/pl unknown
- 2008-09-29 BR BRPI0819087A patent/BRPI0819087B1/pt active IP Right Grant
- 2008-10-07 TW TW097138529A patent/TWI441652B/zh active
-
2014
- 2014-10-22 JP JP2014214975A patent/JP6097734B2/ja active Active
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