KR101293347B1 - 알킬 변성 카복실기 함유 수용성 공중합체 - Google Patents
알킬 변성 카복실기 함유 수용성 공중합체 Download PDFInfo
- Publication number
- KR101293347B1 KR101293347B1 KR1020087014902A KR20087014902A KR101293347B1 KR 101293347 B1 KR101293347 B1 KR 101293347B1 KR 1020087014902 A KR1020087014902 A KR 1020087014902A KR 20087014902 A KR20087014902 A KR 20087014902A KR 101293347 B1 KR101293347 B1 KR 101293347B1
- Authority
- KR
- South Korea
- Prior art keywords
- alkyl
- carboxyl group
- containing water
- modified carboxyl
- soluble copolymer
- 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.)
- Expired - Fee Related
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- 229920001577 copolymer Polymers 0.000 title claims abstract description 72
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 title claims abstract description 62
- 239000007788 liquid Substances 0.000 claims abstract description 31
- 238000002834 transmittance Methods 0.000 claims abstract description 30
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 claims abstract description 28
- 230000003472 neutralizing effect Effects 0.000 claims abstract description 23
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 20
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims abstract description 19
- 150000001875 compounds Chemical class 0.000 claims abstract description 15
- 239000011780 sodium chloride Substances 0.000 claims abstract description 14
- 239000002562 thickening agent Substances 0.000 claims abstract description 12
- 230000035699 permeability Effects 0.000 claims abstract description 8
- 230000000379 polymerizing effect Effects 0.000 claims abstract description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 24
- RFIMISVNSAUMBU-UHFFFAOYSA-N 2-(hydroxymethyl)-2-(prop-2-enoxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC=C RFIMISVNSAUMBU-UHFFFAOYSA-N 0.000 claims description 13
- 238000000034 method Methods 0.000 claims description 6
- 239000003513 alkali Substances 0.000 claims description 4
- XSSOJMFOKGTAFU-UHFFFAOYSA-N 3-[2-(2-prop-2-enoxyethoxy)ethoxy]prop-1-ene Chemical compound C=CCOCCOCCOCC=C XSSOJMFOKGTAFU-UHFFFAOYSA-N 0.000 claims description 3
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 claims description 3
- 239000002202 Polyethylene glycol Substances 0.000 claims description 3
- 229930006000 Sucrose Natural products 0.000 claims description 3
- 229920001223 polyethylene glycol Polymers 0.000 claims description 3
- 239000005720 sucrose Substances 0.000 claims description 3
- 239000003792 electrolyte Substances 0.000 abstract description 29
- -1 lauryl (meth) acrylic acid Chemical compound 0.000 abstract description 9
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 54
- 238000003756 stirring Methods 0.000 description 26
- 230000000052 comparative effect Effects 0.000 description 25
- PUPZLCDOIYMWBV-UHFFFAOYSA-N (+/-)-1,3-Butanediol Chemical compound CC(O)CCO PUPZLCDOIYMWBV-UHFFFAOYSA-N 0.000 description 16
- 238000006243 chemical reaction Methods 0.000 description 15
- 238000005191 phase separation Methods 0.000 description 14
- 239000008213 purified water Substances 0.000 description 14
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 12
- 238000011156 evaluation Methods 0.000 description 12
- 239000003755 preservative agent Substances 0.000 description 12
- 230000002335 preservative effect Effects 0.000 description 12
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 11
- 230000001953 sensory effect Effects 0.000 description 11
- 238000012360 testing method Methods 0.000 description 11
- 239000002537 cosmetic Substances 0.000 description 10
- 239000000243 solution Substances 0.000 description 10
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 9
- GMSCBRSQMRDRCD-UHFFFAOYSA-N dodecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCOC(=O)C(C)=C GMSCBRSQMRDRCD-UHFFFAOYSA-N 0.000 description 9
- 238000005259 measurement Methods 0.000 description 9
- 229940058015 1,3-butylene glycol Drugs 0.000 description 8
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 8
- 229940114077 acrylic acid Drugs 0.000 description 8
- 235000019437 butane-1,3-diol Nutrition 0.000 description 8
- 239000006071 cream Substances 0.000 description 8
- 239000000843 powder Substances 0.000 description 8
- 239000002994 raw material Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 235000011187 glycerol Nutrition 0.000 description 6
- 239000002904 solvent Substances 0.000 description 6
- 235000021355 Stearic acid Nutrition 0.000 description 5
- 229960000541 cetyl alcohol Drugs 0.000 description 5
- 239000000499 gel Substances 0.000 description 5
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 description 5
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 5
- VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical compound CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 5
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 5
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 5
- 239000003505 polymerization initiator Substances 0.000 description 5
- 239000008117 stearic acid Substances 0.000 description 5
- 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 4
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 4
- 229940048053 acrylate Drugs 0.000 description 4
- NOPFSRXAKWQILS-UHFFFAOYSA-N docosan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCO NOPFSRXAKWQILS-UHFFFAOYSA-N 0.000 description 4
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 4
- 239000000839 emulsion Substances 0.000 description 4
- 229940075507 glyceryl monostearate Drugs 0.000 description 4
- ZXEKIIBDNHEJCQ-UHFFFAOYSA-N isobutanol Chemical compound CC(C)CO ZXEKIIBDNHEJCQ-UHFFFAOYSA-N 0.000 description 4
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 4
- 229940031439 squalene Drugs 0.000 description 4
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
- MLSJBGYKDYSOAE-DCWMUDTNSA-N L-Ascorbic acid-2-glucoside Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O[C@@H]2[C@@H]([C@@H](O)[C@H](O)[C@@H](CO)O2)O)=C1O MLSJBGYKDYSOAE-DCWMUDTNSA-N 0.000 description 3
- KWYUFKZDYYNOTN-UHFFFAOYSA-M Potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 3
- 235000013871 bee wax Nutrition 0.000 description 3
- 239000012166 beeswax Substances 0.000 description 3
- 125000003438 dodecyl group Chemical group [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])* 0.000 description 3
- 238000010438 heat treatment Methods 0.000 description 3
- 230000001771 impaired effect Effects 0.000 description 3
- 239000011261 inert gas Substances 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 239000000178 monomer Substances 0.000 description 3
- 229910000403 monosodium phosphate Inorganic materials 0.000 description 3
- 235000019799 monosodium phosphate Nutrition 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- AJPJDKMHJJGVTQ-UHFFFAOYSA-M sodium dihydrogen phosphate Chemical compound [Na+].OP(O)([O-])=O AJPJDKMHJJGVTQ-UHFFFAOYSA-M 0.000 description 3
- MTCFGRXMJLQNBG-REOHCLBHSA-N (2S)-2-Amino-3-hydroxypropansäure Chemical compound OC[C@H](N)C(O)=O MTCFGRXMJLQNBG-REOHCLBHSA-N 0.000 description 2
- XKRFYHLGVUSROY-UHFFFAOYSA-N Argon Chemical compound [Ar] XKRFYHLGVUSROY-UHFFFAOYSA-N 0.000 description 2
- RGSFGYAAUTVSQA-UHFFFAOYSA-N Cyclopentane Chemical compound C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 2
- IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 2
- 229920001214 Polysorbate 60 Polymers 0.000 description 2
- 229920002125 Sokalan® Polymers 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 150000001253 acrylic acids Chemical class 0.000 description 2
- 229920000800 acrylic rubber Polymers 0.000 description 2
- 239000000654 additive Substances 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 239000012298 atmosphere Substances 0.000 description 2
- 229920003123 carboxymethyl cellulose sodium Polymers 0.000 description 2
- 229940063834 carboxymethylcellulose sodium Drugs 0.000 description 2
- 239000004203 carnauba wax Substances 0.000 description 2
- 235000013869 carnauba wax Nutrition 0.000 description 2
- 239000008367 deionised water Substances 0.000 description 2
- 229910021641 deionized water Inorganic materials 0.000 description 2
- 229910001873 dinitrogen Inorganic materials 0.000 description 2
- 229960000735 docosanol Drugs 0.000 description 2
- 239000006260 foam Substances 0.000 description 2
- IPCSVZSSVZVIGE-UHFFFAOYSA-N hexadecanoic acid Chemical compound CCCCCCCCCCCCCCCC(O)=O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 239000004137 magnesium phosphate Substances 0.000 description 2
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- 229910000157 magnesium phosphate Inorganic materials 0.000 description 2
- 229920003145 methacrylic acid copolymer Polymers 0.000 description 2
- HMZGPNHSPWNGEP-UHFFFAOYSA-N octadecyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)C(C)=C HMZGPNHSPWNGEP-UHFFFAOYSA-N 0.000 description 2
- 230000003287 optical effect Effects 0.000 description 2
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- 229910052708 sodium Inorganic materials 0.000 description 2
- 239000011734 sodium Substances 0.000 description 2
- 239000001509 sodium citrate Substances 0.000 description 2
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- DSEKYWAQQVUQTP-XEWMWGOFSA-N (2r,4r,4as,6as,6as,6br,8ar,12ar,14as,14bs)-2-hydroxy-4,4a,6a,6b,8a,11,11,14a-octamethyl-2,4,5,6,6a,7,8,9,10,12,12a,13,14,14b-tetradecahydro-1h-picen-3-one Chemical compound C([C@H]1[C@]2(C)CC[C@@]34C)C(C)(C)CC[C@]1(C)CC[C@]2(C)[C@H]4CC[C@@]1(C)[C@H]3C[C@@H](O)C(=O)[C@@H]1C DSEKYWAQQVUQTP-XEWMWGOFSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- TYMYJUHDFROXOO-UHFFFAOYSA-N 1,3-bis(prop-2-enoxy)-2,2-bis(prop-2-enoxymethyl)propane Chemical compound C=CCOCC(COCC=C)(COCC=C)COCC=C TYMYJUHDFROXOO-UHFFFAOYSA-N 0.000 description 1
- UYZQWKKNVBJVOF-UHFFFAOYSA-N 1-decoxytetradecane Chemical compound CCCCCCCCCCCCCCOCCCCCCCCCC UYZQWKKNVBJVOF-UHFFFAOYSA-N 0.000 description 1
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 1
- JHSWSKVODYPNDV-UHFFFAOYSA-N 2,2-bis(prop-2-enoxymethyl)propane-1,3-diol Chemical compound C=CCOCC(CO)(CO)COCC=C JHSWSKVODYPNDV-UHFFFAOYSA-N 0.000 description 1
- LRZBIPQJHILPJI-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-(2,3-dihydroxypropyl)octadecanoate Chemical compound CCCCCCCCCCCCCCCCC(CC(O)CO)C(=O)OCC(O)CO LRZBIPQJHILPJI-UHFFFAOYSA-N 0.000 description 1
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- XDAVBNHKLPHGGU-UHFFFAOYSA-N 2-methylpentadec-2-enoic acid Chemical compound CCCCCCCCCCCCC=C(C)C(O)=O XDAVBNHKLPHGGU-UHFFFAOYSA-N 0.000 description 1
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 1
- CYDQOEWLBCCFJZ-UHFFFAOYSA-N 4-(4-fluorophenyl)oxane-4-carboxylic acid Chemical compound C=1C=C(F)C=CC=1C1(C(=O)O)CCOCC1 CYDQOEWLBCCFJZ-UHFFFAOYSA-N 0.000 description 1
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- 244000060011 Cocos nucifera Species 0.000 description 1
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- 239000004386 Erythritol Substances 0.000 description 1
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- TUNFSRHWOTWDNC-UHFFFAOYSA-N Myristic acid Natural products CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
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- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- HVUMOYIDDBPOLL-XWVZOOPGSA-N Sorbitan monostearate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O HVUMOYIDDBPOLL-XWVZOOPGSA-N 0.000 description 1
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- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
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- 150000008064 anhydrides Chemical class 0.000 description 1
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- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
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- LVTYICIALWPMFW-UHFFFAOYSA-N diisopropanolamine Chemical compound CC(O)CNCC(C)O LVTYICIALWPMFW-UHFFFAOYSA-N 0.000 description 1
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- UNXHWFMMPAWVPI-ZXZARUISSA-N erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
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- IUJAMGNYPWYUPM-UHFFFAOYSA-N hentriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC IUJAMGNYPWYUPM-UHFFFAOYSA-N 0.000 description 1
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- XJNUECKWDBNFJV-UHFFFAOYSA-N hexadecyl 2-ethylhexanoate Chemical compound CCCCCCCCCCCCCCCCOC(=O)C(CC)CCCC XJNUECKWDBNFJV-UHFFFAOYSA-N 0.000 description 1
- 230000002209 hydrophobic effect Effects 0.000 description 1
- UCNNJGDEJXIUCC-UHFFFAOYSA-L hydroxy(oxo)iron;iron Chemical compound [Fe].O[Fe]=O.O[Fe]=O UCNNJGDEJXIUCC-UHFFFAOYSA-L 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
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- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- 230000003993 interaction Effects 0.000 description 1
- 229910000358 iron sulfate Inorganic materials 0.000 description 1
- BAUYGSIQEAFULO-UHFFFAOYSA-L iron(2+) sulfate (anhydrous) Chemical compound [Fe+2].[O-]S([O-])(=O)=O BAUYGSIQEAFULO-UHFFFAOYSA-L 0.000 description 1
- WTFXARWRTYJXII-UHFFFAOYSA-N iron(2+);iron(3+);oxygen(2-) Chemical compound [O-2].[O-2].[O-2].[O-2].[Fe+2].[Fe+3].[Fe+3] WTFXARWRTYJXII-UHFFFAOYSA-N 0.000 description 1
- SZVJSHCCFOBDDC-UHFFFAOYSA-N iron(II,III) oxide Inorganic materials O=[Fe]O[Fe]O[Fe]=O SZVJSHCCFOBDDC-UHFFFAOYSA-N 0.000 description 1
- YOBAEOGBNPPUQV-UHFFFAOYSA-N iron;trihydrate Chemical compound O.O.O.[Fe].[Fe] YOBAEOGBNPPUQV-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
- 235000010994 magnesium phosphates Nutrition 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 239000004200 microcrystalline wax Substances 0.000 description 1
- 235000019808 microcrystalline wax Nutrition 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000001333 moisturizer Effects 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 239000012299 nitrogen atmosphere Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- 229940093429 polyethylene glycol 6000 Drugs 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 239000007870 radical polymerization initiator Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 108700004121 sarkosyl Proteins 0.000 description 1
- 229960001153 serine Drugs 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- 239000001540 sodium lactate Substances 0.000 description 1
- 229940005581 sodium lactate Drugs 0.000 description 1
- 235000011088 sodium lactate Nutrition 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 235000013599 spices Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
- OGIDPMRJRNCKJF-UHFFFAOYSA-N titanium oxide Inorganic materials [Ti]=O OGIDPMRJRNCKJF-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 239000003871 white petrolatum Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
Classifications
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- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
- C08F220/06—Acrylic acid; Methacrylic acid; Metal salts or ammonium salts thereof
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- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/8141—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8152—Homopolymers or copolymers of esters, e.g. (meth)acrylic acid esters; Compositions of derivatives of such polymers
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- A61Q19/00—Preparations for care of the skin
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- 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
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/04—Acids; Metal salts or ammonium salts thereof
-
- 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
- C08F8/00—Chemical modification by after-treatment
- C08F8/42—Introducing metal atoms or metal-containing groups
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/48—Thickener, Thickening system
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- A—HUMAN NECESSITIES
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
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- A61Q1/02—Preparations containing skin colorants, e.g. pigments
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/04—Preparations containing skin colorants, e.g. pigments for lips
- A61Q1/06—Lipsticks
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- A—HUMAN NECESSITIES
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- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q1/00—Make-up preparations; Body powders; Preparations for removing make-up
- A61Q1/02—Preparations containing skin colorants, e.g. pigments
- A61Q1/10—Preparations containing skin colorants, e.g. pigments for eyes, e.g. eyeliner, mascara
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/04—Topical preparations for affording protection against sunlight or other radiation; Topical sun tanning preparations
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- 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
- A61Q19/10—Washing or bathing preparations
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
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- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/12—Esters of monohydric alcohols or phenols
- C08F220/16—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
- C08F220/18—Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
- C08F220/1812—C12-(meth)acrylate, e.g. lauryl (meth)acrylate
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Abstract
Description
주요 원료 | 참고예 a | 참고예 b | 실시예 3 | 실시예 4 |
아크릴산(g) | 45(100) | 45(100) | 45(100) | 45(100) |
메타크릴산라우릴(g) | 2.7(6) | 4.1(9.1) | 2.7(6) | 4.1(9.1) |
펜타에리스리톨알릴에터(g) | - | - | 0.02(0.044) | 0.02(0.044) |
주요 원료 | 비교예 1 | 비교예 2 | 비교예 3 | 비교예 4 | 비교예 5 |
아크릴산(g) | 45(100) | 45(100) | 45(100) | 45(100) | 45(100) |
메타크릴산라우릴(g) | 1.8(4) | 5.4(12) | 2.7(6) | - | - |
메타크릴산스테아릴(g) | - | - | - | 4.1(9.1) | 0.9(2) |
펜타에리스리톨알릴에터(g) | - | - | 0.13(0.29) | 0.02(0.044) | 0.09(0.2) |
NaCl 첨가량 [g] |
참고예 a | 참고예 b | ||||
점도 [mPaㆍs] |
투과율 [%] |
비고 | 점도 [mPaㆍs] |
투과율 [%] |
비고 | |
0 | 110 | 99 | 250 | 99 | ||
3 6 9 12 15 18 21 |
4310 17000 18700 14100 9700 5500 1600 |
98 97 98 96 96 94 92 |
관능 시험 시료 |
25000 14250 7100 4000 2250 1800 1500 |
97 96 95 94 92 91 90 |
관능 시험 시료 |
NaCl 첨가량 [g] |
실시예 3 | 실시예 4 | ||||
점도 [mPaㆍs] |
투과율 [%] |
비고 | 점도 [mPaㆍs] |
투과율 [%] |
비고 | |
0 | 240 | 99 | 300 | 99 | ||
3 6 9 12 15 18 21 |
2940 16750 19300 15000 10450 7650 3760 |
98 98 96 95 94 92 90 |
관능 시험 시료 |
26500 15000 6900 4500 2000 1900 1200 |
98 97 92 94 91 91 90 |
관능 시험 시료 |
NaCl 첨가량 [g] |
비교예 1 | 비교예 2 | ||||
점도 [mPaㆍs] |
투과율 [%] |
비고 | 점도 [mPaㆍs] |
투과율 [%] |
비고 | |
0 | 188 | 99 | 340 | 97 | ||
3 6 9 12 15 18 21 |
44 106 776 2990 4800 8000 7250 |
98 98 96 95 94 92 90 |
관능 시험 시료 |
18550 4340 2900 800 - - - |
84 57 34 8 - - - |
관능 시험 시료 상분리 상분리 상분리 |
NaCl 첨가량 [g] |
비교예 3 | 비교예 4 | ||||
점도 [mPaㆍs] |
투과율 [%] |
비고 | 점도 [mPaㆍs] |
투과율 [%] |
비고 | |
0 | 5700 | 96 | 15200 | 97 | 관능 시험 시료 | |
3 6 9 12 15 18 21 |
7100 4900 2200 50 - - - |
88 65 13 2 - - - |
관능 시험 시료 상분리 상분리 상분리 |
6800 250 - - - - - |
56 14 - - - - - |
상분리 상분리 상분리 상분리 상분리 |
NaCl 첨가량 [g] |
비교예 5 | ||
점도 [mPaㆍs] |
투과율 [%] |
비고 | |
0 | 6800 | 95 | |
3 6 9 12 15 18 21 |
9550 6150 1700 400 - - - |
87 63 13 4 - - - |
관능 시험 시료 상분리 상분리 상분리 |
평가 기준 | 참고예 a [사람수] |
참고예 b [사람수] |
실시예 3 [사람수] |
실시예 4 [사람수] |
◎ | 9 | 0 | 7 | 1 |
○ | 1 | 8 | 2 | 7 |
△ | 0 | 2 | 1 | 2 |
× | 0 | 0 | 0 | 0 |
평가 기준 | 비교예 1 [사람수] |
비교예 2 [사람수] |
비교예 3 [사람수] |
비교예 4 [사람수] |
비교예 5 [사람수] |
◎ | 8 | 8 | 8 | 1 | 7 |
○ | 2 | 1 | 1 | 0 | 2 |
△ | 0 | 1 | 1 | 1 | 1 |
× | 0 | 0 | 0 | 8 | 0 |
Claims (3)
- (메트)아크릴산 100중량부와, (메트)아크릴산라우릴 5~10중량부와, 0~0.1중량부의 에틸렌성 불포화기를 2개 이상 갖는 화합물을 중합시켜 얻어지는 알킬 변성 카복실기 함유 수용성 공중합체로서,에틸렌성 불포화기를 2개 이상 갖는 화합물의 사용량은 (메트)아크릴산 100중량부에 대하여 0.001~0.044중량부이고,1중량% 중화 점조액의 점도가 1000mPaㆍs 이하이며 투과율이 95% 이상, 또한, 상기 중화 점조액 100중량부에 대하여 1~7중량부의 염화나트륨을 첨가했을 때의 최고 점도가 10000~30000mPaㆍs이며 투과율이 95% 이상이고,상기 1중량% 중화 점조액은 상기 공중합체를 순수에 용해시켜, 알칼리로 pH 6.5~7.5로 중화시킨 상기 공중합체의 농도가 1중량%인 중화 점조액인,알킬 변성 카복실기 함유 수용성 공중합체.
- 제 1 항에 있어서,에틸렌성 불포화기를 2개 이상 갖는 화합물이, 펜타에리스리톨알릴에터, 다이에틸렌글라이콜다이알릴에터, 폴리에틸렌글라이콜다이알릴에터 및 폴리알릴수크로스로 이루어지는 군에서 선택된 적어도 1종인 알킬 변성 카복실기 함유 수용성 공중합체.
- 제 1 항 또는 제 2 항에 기재된 알킬 변성 카복실기 함유 수용성 공중합체를 포함하는 증점제.
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JP2005335628 | 2005-11-21 | ||
JPJP-P-2005-00335628 | 2005-11-21 | ||
PCT/JP2006/322557 WO2007058143A1 (ja) | 2005-11-21 | 2006-11-13 | アルキル変性カルボキシル基含有水溶性共重合体 |
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KR101293347B1 true KR101293347B1 (ko) | 2013-08-05 |
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US (1) | US8067517B2 (ko) |
EP (1) | EP1953176B1 (ko) |
JP (1) | JP5149626B2 (ko) |
KR (1) | KR101293347B1 (ko) |
CN (1) | CN101312996B (ko) |
CA (1) | CA2629081C (ko) |
WO (1) | WO2007058143A1 (ko) |
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CA2627792C (en) * | 2005-11-14 | 2013-12-31 | Sumitomo Seika Chemicals Co., Ltd. | Water-soluble copolymer having alkyl-modified carboxyl groups |
BR112012031623B1 (pt) | 2010-06-11 | 2018-04-10 | The Procter & Gamble Company | Composição para cuidados pessoais e seu uso |
FR2983406B1 (fr) * | 2011-12-05 | 2014-03-28 | Oreal | Composition cosmetique de revetement des fibres keratiniques |
CA2880386A1 (en) * | 2012-08-03 | 2014-02-06 | Sumitomo Seika Chemicals Co., Ltd. | Viscous composition |
CN103105751B (zh) * | 2012-12-27 | 2014-09-24 | 深圳市乐普泰科技股份有限公司 | 核壳结构悬浮聚合墨粉制备方法 |
DE102013206314A1 (de) | 2013-04-10 | 2014-10-16 | Evonik Industries Ag | Kosmetische Formulierung enthaltend Copolymer sowie Sulfosuccinat und/oder Biotensid |
EP3015525A4 (en) * | 2013-06-28 | 2016-11-02 | Sumitomo Seika Chemicals | HYDROPHILIC THICKENER AND COSMETIC COMPOSITION THEREWITH |
US10966916B2 (en) | 2014-11-10 | 2021-04-06 | The Procter And Gamble Company | Personal care compositions |
WO2016077325A1 (en) | 2014-11-10 | 2016-05-19 | The Procter & Gamble Company | Personal care compositions with two benefit phases |
EP3217949B1 (en) | 2014-11-10 | 2020-06-17 | The Procter and Gamble Company | Personal care compositions with two benefit phases |
WO2016077329A1 (en) | 2014-11-10 | 2016-05-19 | The Procter & Gamble Company | Personal care compositions |
CN111212625B (zh) | 2017-10-20 | 2023-05-23 | 宝洁公司 | 气溶胶泡沫洁肤剂 |
WO2019079405A1 (en) | 2017-10-20 | 2019-04-25 | The Procter & Gamble Company | AEROSOL FOAMING CLEANSER FOR THE SKIN |
EP3720568B1 (en) | 2017-12-08 | 2022-01-12 | The Procter & Gamble Company | Methods of screening for mild skin cleanser |
CN113015904B (zh) | 2018-11-29 | 2024-06-18 | 宝洁公司 | 用于筛选个人护理产品的方法 |
WO2022270640A2 (ja) * | 2022-03-17 | 2022-12-29 | 富士フイルム和光純薬株式会社 | 高分子化合物、化粧料、増粘剤 |
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JP2005126455A (ja) | 2003-10-21 | 2005-05-19 | Sumitomo Seika Chem Co Ltd | カルボキシル基含有水溶性重合体の製造法 |
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US3940351A (en) * | 1974-07-02 | 1976-02-24 | The B. F. Goodrich Company | Polymerization of carboxylic acid monomers and alkyl acrylate esters in chlorofluoroethane |
US4190562A (en) * | 1977-04-04 | 1980-02-26 | The B. F. Goodrich Company | Improved water absorbent copolymers of copolymerizable carboxylic acids and acrylic or methacrylic esters |
US4066583A (en) * | 1977-05-16 | 1978-01-03 | The B. F. Goodrich Company | Flexible water absorbent polymer compositions comprising (a) unsaturated carboxylic acid, acrylic ester containing alkyl group 10-30 carbon atoms, additional monomer plus (b) aliphatic diol |
JPS57174306A (en) * | 1981-04-20 | 1982-10-27 | Ricoh Co Ltd | Production of nonaqueous resin dispersion |
EP0099179A3 (en) * | 1982-06-22 | 1987-01-21 | Imperial Chemical Industries Plc | Particulate dispersions |
US4509949A (en) * | 1983-06-13 | 1985-04-09 | The B. F. Goodrich Company | Water thickening agents consisting of copolymers of crosslinked acrylic acids and esters |
US5004598A (en) | 1986-11-10 | 1991-04-02 | The B. F. Goodrich Company | Stable and quick-breaking topical skin compositions |
US4996274A (en) | 1988-02-19 | 1991-02-26 | The B. F. Goodrich Company | Polycarboxylic acids with higher thickening capacity and better clarity |
GB8813966D0 (en) * | 1988-06-13 | 1988-07-20 | Nat Starch Chem Corp | Process for manufacture of polymers |
JPH0439312A (ja) | 1990-06-06 | 1992-02-10 | Showa Denko Kk | 架橋型アクリル酸系ポリマー及びそれを用いた化粧料 |
US5618877A (en) | 1994-10-24 | 1997-04-08 | Amcol International Corporation | Process for polymerization of water-soluble and water-insoluble carboxylic acid polymers and copolymers in a silicone oil solvent |
US6018010A (en) * | 1995-04-26 | 2000-01-25 | Nippon Shokubai Co., Ltd. | Polymer with high acid value from unsaturated carboxylic acid and vinyl monomer |
DE19538607A1 (de) * | 1995-10-18 | 1997-04-24 | Hoechst Ag | Polymerverdicktes Enteisungsmittel und Vereisungsschutzmittel für Flugzeuge |
JP2001181123A (ja) | 1999-12-27 | 2001-07-03 | Lion Corp | 外用剤組成物 |
JPWO2003016382A1 (ja) * | 2001-08-09 | 2004-12-02 | 住友精化株式会社 | 架橋型カルボキシル基含有重合体粒子 |
JP4560815B2 (ja) * | 2004-07-27 | 2010-10-13 | 日本純薬株式会社 | 粉末状(メタ)アクリル酸系共重合体の製造方法及びその共重合体、並びに高分子乳化剤 |
JP4759236B2 (ja) * | 2004-07-28 | 2011-08-31 | 住友精化株式会社 | カルボキシル基含有水溶性重合体の製造方法 |
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- 2006-11-13 KR KR1020087014902A patent/KR101293347B1/ko not_active Expired - Fee Related
- 2006-11-13 CN CN2006800435810A patent/CN101312996B/zh not_active Expired - Fee Related
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- 2006-11-13 JP JP2007545230A patent/JP5149626B2/ja not_active Expired - Fee Related
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US3915921A (en) * | 1974-07-02 | 1975-10-28 | Goodrich Co B F | Unsaturated carboxylic acid-long chain alkyl ester copolymers and tri-polymers water thickening agents and emulsifiers |
JP2003268009A (ja) | 2002-03-18 | 2003-09-25 | Sumitomo Seika Chem Co Ltd | カルボキシル基含有水溶性重合体の製造方法 |
JP2004281055A (ja) | 2003-01-23 | 2004-10-07 | Hitachi Chem Co Ltd | カルボキシル基含有樹脂を用いた電池用バインダ樹脂組成物、合剤スラリー、電極および電池 |
JP2005126455A (ja) | 2003-10-21 | 2005-05-19 | Sumitomo Seika Chem Co Ltd | カルボキシル基含有水溶性重合体の製造法 |
Also Published As
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KR20080078680A (ko) | 2008-08-27 |
JP5149626B2 (ja) | 2013-02-20 |
EP1953176A4 (en) | 2009-07-01 |
CA2629081C (en) | 2013-12-31 |
CN101312996B (zh) | 2011-03-09 |
CA2629081A1 (en) | 2007-05-24 |
EP1953176A1 (en) | 2008-08-06 |
EP1953176B1 (en) | 2011-07-06 |
JPWO2007058143A1 (ja) | 2009-04-30 |
US20090292078A1 (en) | 2009-11-26 |
CN101312996A (zh) | 2008-11-26 |
US8067517B2 (en) | 2011-11-29 |
WO2007058143A1 (ja) | 2007-05-24 |
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