ES2266904T3 - Polimeros polivalentes, metodos y composiciones. - Google Patents
Polimeros polivalentes, metodos y composiciones. Download PDFInfo
- Publication number
- ES2266904T3 ES2266904T3 ES03795628T ES03795628T ES2266904T3 ES 2266904 T3 ES2266904 T3 ES 2266904T3 ES 03795628 T ES03795628 T ES 03795628T ES 03795628 T ES03795628 T ES 03795628T ES 2266904 T3 ES2266904 T3 ES 2266904T3
- Authority
- ES
- Spain
- Prior art keywords
- alkyl
- polymer
- composition
- mixture
- monomer
- 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 - Lifetime
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- 229920000642 polymer Polymers 0.000 title claims abstract description 423
- 239000000203 mixture Substances 0.000 title claims abstract description 408
- 238000000034 method Methods 0.000 title claims description 35
- 239000000178 monomer Substances 0.000 claims abstract description 240
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 97
- 229920002554 vinyl polymer Polymers 0.000 claims abstract description 83
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 78
- 239000004094 surface-active agent Substances 0.000 claims abstract description 71
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 37
- 150000001875 compounds Chemical class 0.000 claims abstract description 27
- 150000002148 esters Chemical class 0.000 claims abstract description 27
- 238000006116 polymerization reaction Methods 0.000 claims abstract description 25
- 125000003118 aryl group Chemical group 0.000 claims abstract description 23
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 23
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 18
- 125000005702 oxyalkylene group Chemical group 0.000 claims abstract description 12
- 125000001424 substituent group Chemical group 0.000 claims abstract description 12
- 229920001400 block copolymer Polymers 0.000 claims abstract description 10
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims abstract description 10
- 229920001519 homopolymer Polymers 0.000 claims abstract description 10
- 229920005604 random copolymer Polymers 0.000 claims abstract description 10
- 125000003545 alkoxy group Chemical group 0.000 claims abstract description 9
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 claims abstract description 8
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims abstract description 7
- 125000005843 halogen group Chemical group 0.000 claims abstract description 6
- -1 2-pyrrolidonyl Chemical group 0.000 claims description 186
- 210000004209 hair Anatomy 0.000 claims description 148
- 239000003795 chemical substances by application Substances 0.000 claims description 130
- 239000000839 emulsion Substances 0.000 claims description 90
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 75
- 238000009472 formulation Methods 0.000 claims description 58
- 229910052757 nitrogen Inorganic materials 0.000 claims description 56
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 54
- 150000003839 salts Chemical group 0.000 claims description 40
- 230000003750 conditioning effect Effects 0.000 claims description 36
- 239000000126 substance Substances 0.000 claims description 32
- 238000004140 cleaning Methods 0.000 claims description 30
- 239000003381 stabilizer Substances 0.000 claims description 30
- 239000002562 thickening agent Substances 0.000 claims description 30
- 239000002537 cosmetic Substances 0.000 claims description 28
- 239000003921 oil Substances 0.000 claims description 28
- 229920001577 copolymer Polymers 0.000 claims description 26
- 239000002904 solvent Substances 0.000 claims description 25
- 239000000463 material Substances 0.000 claims description 23
- 239000007788 liquid Substances 0.000 claims description 22
- 238000004132 cross linking Methods 0.000 claims description 21
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 19
- 239000007787 solid Substances 0.000 claims description 19
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 18
- 239000010408 film Substances 0.000 claims description 18
- 239000003995 emulsifying agent Substances 0.000 claims description 16
- 238000007720 emulsion polymerization reaction Methods 0.000 claims description 16
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 claims description 15
- 150000002734 metacrylic acid derivatives Polymers 0.000 claims description 15
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical group OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 claims description 14
- 230000008569 process Effects 0.000 claims description 14
- 239000006254 rheological additive Substances 0.000 claims description 14
- 238000011282 treatment Methods 0.000 claims description 14
- 238000000576 coating method Methods 0.000 claims description 13
- 239000006260 foam Substances 0.000 claims description 13
- 239000002736 nonionic surfactant Substances 0.000 claims description 13
- 150000005846 sugar alcohols Polymers 0.000 claims description 13
- 150000001252 acrylic acid derivatives Polymers 0.000 claims description 12
- 239000003945 anionic surfactant Substances 0.000 claims description 12
- 239000012986 chain transfer agent Substances 0.000 claims description 12
- 239000003999 initiator Substances 0.000 claims description 12
- 125000000129 anionic group Chemical group 0.000 claims description 11
- 238000002360 preparation method Methods 0.000 claims description 11
- 239000003981 vehicle Substances 0.000 claims description 11
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 claims description 10
- 150000003856 quaternary ammonium compounds Chemical class 0.000 claims description 10
- 238000000518 rheometry Methods 0.000 claims description 10
- 239000004909 Moisturizer Substances 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 230000001333 moisturizer Effects 0.000 claims description 9
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 9
- 239000003380 propellant Substances 0.000 claims description 9
- 239000000375 suspending agent Substances 0.000 claims description 9
- 238000006243 chemical reaction Methods 0.000 claims description 8
- 239000007921 spray Substances 0.000 claims description 8
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 7
- 125000004103 aminoalkyl group Chemical group 0.000 claims description 7
- 239000011248 coating agent Substances 0.000 claims description 7
- 125000000623 heterocyclic group Chemical group 0.000 claims description 7
- 230000004048 modification Effects 0.000 claims description 7
- 238000012986 modification Methods 0.000 claims description 7
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 6
- 125000005907 alkyl ester group Chemical group 0.000 claims description 6
- 239000006172 buffering agent Substances 0.000 claims description 6
- 229910052799 carbon Inorganic materials 0.000 claims description 6
- 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 claims description 6
- 229910052736 halogen Inorganic materials 0.000 claims description 6
- 230000036541 health Effects 0.000 claims description 6
- 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 claims description 6
- 125000004079 stearyl 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])C([H])([H])C([H])([H])[H] 0.000 claims description 6
- CMVNWVONJDMTSH-UHFFFAOYSA-N 7-bromo-2-methyl-1h-quinazolin-4-one Polymers C1=CC(Br)=CC2=NC(C)=NC(O)=C21 CMVNWVONJDMTSH-UHFFFAOYSA-N 0.000 claims description 5
- 235000014698 Brassica juncea var multisecta Nutrition 0.000 claims description 5
- 235000006008 Brassica napus var napus Nutrition 0.000 claims description 5
- 240000000385 Brassica napus var. napus Species 0.000 claims description 5
- 235000006618 Brassica rapa subsp oleifera Nutrition 0.000 claims description 5
- 235000004977 Brassica sinapistrum Nutrition 0.000 claims description 5
- 239000002280 amphoteric surfactant Substances 0.000 claims description 5
- 239000004359 castor oil Substances 0.000 claims description 5
- 235000019438 castor oil Nutrition 0.000 claims description 5
- 235000012000 cholesterol Nutrition 0.000 claims description 5
- 239000000834 fixative Substances 0.000 claims description 5
- 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 claims description 5
- 229920006254 polymer film Polymers 0.000 claims description 5
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 5
- UROPHWSHWQXFDR-UHFFFAOYSA-N 2-methylprop-2-enoic acid;phenol Chemical compound CC(=C)C(O)=O.OC1=CC=CC=C1 UROPHWSHWQXFDR-UHFFFAOYSA-N 0.000 claims description 4
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical group CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 4
- 125000001204 arachidyl 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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 4
- 239000002738 chelating agent Substances 0.000 claims description 4
- 239000002270 dispersing agent Substances 0.000 claims description 4
- HJZOFAWRMPYCHL-UHFFFAOYSA-N octacosyl prop-2-enoate Polymers CCCCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=C HJZOFAWRMPYCHL-UHFFFAOYSA-N 0.000 claims description 4
- 239000004753 textile Substances 0.000 claims description 4
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 claims description 3
- JTHZUSWLNCPZLX-UHFFFAOYSA-N 6-fluoro-3-methyl-2h-indazole Polymers FC1=CC=C2C(C)=NNC2=C1 JTHZUSWLNCPZLX-UHFFFAOYSA-N 0.000 claims description 3
- 125000005250 alkyl acrylate group Chemical group 0.000 claims description 3
- OCDWICPYKQMQSQ-UHFFFAOYSA-N docosyl 2-methylprop-2-enoate Polymers CCCCCCCCCCCCCCCCCCCCCCOC(=O)C(C)=C OCDWICPYKQMQSQ-UHFFFAOYSA-N 0.000 claims description 3
- 230000001804 emulsifying effect Effects 0.000 claims description 3
- 229910052739 hydrogen Inorganic materials 0.000 claims description 3
- 229910021645 metal ion Inorganic materials 0.000 claims description 3
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical group CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 3
- 101150009274 nhr-1 gene Proteins 0.000 claims description 3
- 239000003973 paint Substances 0.000 claims description 3
- 239000012736 aqueous medium Substances 0.000 claims description 2
- 239000008406 cosmetic ingredient Substances 0.000 claims description 2
- 125000004185 ester group Chemical group 0.000 claims description 2
- 125000002819 montanyl group Polymers [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])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 claims description 2
- FSAJWMJJORKPKS-UHFFFAOYSA-N octadecyl prop-2-enoate Polymers CCCCCCCCCCCCCCCCCCOC(=O)C=C FSAJWMJJORKPKS-UHFFFAOYSA-N 0.000 claims description 2
- GMMVDHHXYPDRJR-UHFFFAOYSA-N hexacosyl prop-2-enoate Polymers CCCCCCCCCCCCCCCCCCCCCCCCCCOC(=O)C=C GMMVDHHXYPDRJR-UHFFFAOYSA-N 0.000 claims 3
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims 2
- NGYRYRBDIPYKTL-UHFFFAOYSA-N icosyl prop-2-enoate Polymers CCCCCCCCCCCCCCCCCCCCOC(=O)C=C NGYRYRBDIPYKTL-UHFFFAOYSA-N 0.000 claims 2
- ACVYVLVWPXVTIT-UHFFFAOYSA-M phosphinate Chemical compound [O-][PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-M 0.000 claims 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 2
- 125000000923 (C1-C30) alkyl group Chemical group 0.000 abstract 3
- 125000004417 unsaturated alkyl group Chemical group 0.000 abstract 2
- 239000000047 product Substances 0.000 description 161
- 125000002091 cationic group Chemical group 0.000 description 139
- 239000004615 ingredient Substances 0.000 description 118
- 239000002253 acid Substances 0.000 description 78
- 239000000499 gel Substances 0.000 description 71
- 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 63
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 53
- 239000002453 shampoo Substances 0.000 description 52
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 44
- 239000004480 active ingredient Substances 0.000 description 41
- 235000002639 sodium chloride Nutrition 0.000 description 40
- 238000002156 mixing Methods 0.000 description 38
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 33
- 229920001296 polysiloxane Polymers 0.000 description 29
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 28
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 27
- 235000019198 oils Nutrition 0.000 description 26
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 23
- 239000006071 cream Substances 0.000 description 21
- 239000008367 deionised water Substances 0.000 description 20
- 229910021641 deionized water Inorganic materials 0.000 description 20
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 20
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 20
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 20
- 239000003755 preservative agent Substances 0.000 description 20
- 239000011734 sodium Substances 0.000 description 20
- 229910052708 sodium Inorganic materials 0.000 description 20
- 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 19
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- 238000003860 storage Methods 0.000 description 19
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- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 17
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 16
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 16
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 16
- 239000000975 dye Substances 0.000 description 16
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- 230000002378 acidificating effect Effects 0.000 description 15
- 239000003205 fragrance Substances 0.000 description 15
- 239000004205 dimethyl polysiloxane Substances 0.000 description 14
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- 239000006210 lotion Substances 0.000 description 13
- 150000007513 acids Chemical class 0.000 description 12
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- 239000002245 particle Substances 0.000 description 12
- 150000001412 amines Chemical class 0.000 description 11
- 235000015165 citric acid Nutrition 0.000 description 11
- 230000000052 comparative effect Effects 0.000 description 11
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- 235000014113 dietary fatty acids Nutrition 0.000 description 10
- 239000000194 fatty acid Substances 0.000 description 10
- 229930195729 fatty acid Natural products 0.000 description 10
- KWIUHFFTVRNATP-UHFFFAOYSA-N glycine betaine Chemical compound C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 10
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 10
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- 238000012546 transfer Methods 0.000 description 10
- ZPFAVCIQZKRBGF-UHFFFAOYSA-N 1,3,2-dioxathiolane 2,2-dioxide Chemical compound O=S1(=O)OCCO1 ZPFAVCIQZKRBGF-UHFFFAOYSA-N 0.000 description 9
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 9
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- 125000004432 carbon atom Chemical group C* 0.000 description 9
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- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 8
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 8
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- MRUAUOIMASANKQ-UHFFFAOYSA-N cocamidopropyl betaine Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC([O-])=O MRUAUOIMASANKQ-UHFFFAOYSA-N 0.000 description 8
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- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 7
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 7
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical class [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 7
- 239000004902 Softening Agent Substances 0.000 description 7
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- 125000002252 acyl group Chemical group 0.000 description 7
- 229940061720 alpha hydroxy acid Drugs 0.000 description 7
- 150000001280 alpha hydroxy acids Chemical class 0.000 description 7
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 7
- 210000002683 foot Anatomy 0.000 description 7
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- 229910052500 inorganic mineral Inorganic materials 0.000 description 7
- 230000014759 maintenance of location Effects 0.000 description 7
- 230000007935 neutral effect Effects 0.000 description 7
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 7
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2-(2-cyanopropan-2-yldiazenyl)-2-methylpropanenitrile Chemical compound N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 6
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
- 102000008186 Collagen Human genes 0.000 description 6
- 108010035532 Collagen Proteins 0.000 description 6
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N Disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 6
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 6
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 6
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- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 description 1
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Classifications
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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
- C08F8/00—Chemical modification by after-treatment
- C08F8/30—Introducing nitrogen atoms or nitrogen-containing groups
- C08F8/32—Introducing nitrogen atoms or nitrogen-containing groups by reaction with amines
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- 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
- A61K8/72—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
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- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
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- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
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- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
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- General Chemical & Material Sciences (AREA)
- Cosmetics (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Detergent Compositions (AREA)
- Paints Or Removers (AREA)
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| US10/646,856 US7378479B2 (en) | 2002-09-13 | 2003-08-22 | Multi-purpose polymers, methods and compositions |
| US646856 | 2003-08-22 |
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| ES2266904T3 true ES2266904T3 (es) | 2007-03-01 |
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| FR3140277B1 (fr) | 2022-09-30 | 2025-07-25 | Oreal | Composition cosmétique de soin des cheveux comprenant au moins une silicone aminée particulière et au moins un polymère associatif, et procédé de traitement cosmétique des cheveux |
| FR3140281B1 (fr) | 2022-09-30 | 2025-07-25 | Oreal | Procédé de traitement cosmétique des cheveux avec une composition cosmétique comprenant des silicones aminées particulières |
| FR3140274B1 (fr) | 2022-09-30 | 2025-07-25 | Oreal | Composition cosmétique de soin des cheveux comprenant au moins une silicone aminée particulière et au moins un agent épaississant |
| FR3140279B1 (fr) | 2022-09-30 | 2025-07-25 | Oreal | Composition cosmétique de soin des cheveux comprenant au moins une silicone aminée particulière et au moins un corps gras non siliconé, et procédé de traitement cosmétique des cheveux |
| FR3140275B1 (fr) | 2022-09-30 | 2025-08-01 | Oreal | Composition cosmétique de soin des cheveux comprenant des silicones aminées particulières et des silicones additionnelles, et procédé de traitement cosmétique des cheveux. |
| FR3140273B1 (fr) | 2022-09-30 | 2025-07-25 | Oreal | Composition cosmétique de soin des cheveux comprenant au moins une silicone aminée particulière et au moins un agent colorant et/ou un azurant optique, et procédé de traitement cosmétique des cheveux |
| TWI842550B (zh) * | 2023-06-02 | 2024-05-11 | 臺灣塑膠工業股份有限公司 | 抗菌矽膠材料、其製造方法及含其之植入式醫療器材 |
| FR3152399A1 (fr) | 2023-09-04 | 2025-03-07 | L'oreal | Procédé de traitement cosmétique |
| FR3154321A1 (fr) | 2023-10-24 | 2025-04-25 | L'oreal | Procédé de coloration ou de décoloration des fibres kératiniques, comprenant l’application d’une composition comprenant des composés de type aminoacides et des acides carboxyliques hydroxylés |
| WO2025096303A1 (en) | 2023-10-31 | 2025-05-08 | United States Gypsum Company | Alternative means of preservation of coatings/compounds |
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-
2003
- 2003-08-22 US US10/646,856 patent/US7378479B2/en not_active Expired - Lifetime
- 2003-08-25 MX MXPA05002684A patent/MXPA05002684A/es active IP Right Grant
- 2003-08-25 CA CA002498529A patent/CA2498529A1/en not_active Abandoned
- 2003-08-25 WO PCT/US2003/026608 patent/WO2004024779A2/en not_active Ceased
- 2003-08-25 EP EP03795628A patent/EP1581568B1/en not_active Expired - Lifetime
- 2003-08-25 JP JP2004536051A patent/JP4482452B2/ja not_active Expired - Fee Related
- 2003-08-25 DE DE60306687T patent/DE60306687T2/de not_active Expired - Lifetime
- 2003-08-25 BR BRPI0314242A patent/BR0314242B8/pt active IP Right Grant
- 2003-08-25 AU AU2003265662A patent/AU2003265662C1/en not_active Ceased
- 2003-08-25 PL PL03375599A patent/PL375599A1/xx not_active Application Discontinuation
- 2003-08-25 KR KR1020057004327A patent/KR101067958B1/ko not_active Expired - Fee Related
- 2003-08-25 ES ES03795628T patent/ES2266904T3/es not_active Expired - Lifetime
- 2003-08-25 AT AT03795628T patent/ATE332318T1/de not_active IP Right Cessation
- 2003-08-25 RU RU2005110948/04A patent/RU2005110948A/ru not_active Application Discontinuation
- 2003-09-10 TW TW092125003A patent/TW200422310A/zh unknown
- 2003-09-11 AR ARP030103293A patent/AR041233A1/es not_active Application Discontinuation
-
2008
- 2008-05-22 US US12/125,288 patent/US8044156B2/en not_active Expired - Lifetime
Also Published As
| Publication number | Publication date |
|---|---|
| AU2003265662B2 (en) | 2008-12-11 |
| AR041233A1 (es) | 2005-05-11 |
| DE60306687T2 (de) | 2007-06-28 |
| CA2498529A1 (en) | 2004-03-25 |
| US8044156B2 (en) | 2011-10-25 |
| US7378479B2 (en) | 2008-05-27 |
| RU2005110948A (ru) | 2005-10-20 |
| KR101067958B1 (ko) | 2011-09-26 |
| US20040052746A1 (en) | 2004-03-18 |
| US20080233069A1 (en) | 2008-09-25 |
| BR0314242B8 (pt) | 2021-07-27 |
| KR20050054941A (ko) | 2005-06-10 |
| AU2003265662A1 (en) | 2004-04-30 |
| MXPA05002684A (es) | 2005-05-05 |
| ATE332318T1 (de) | 2006-07-15 |
| DE60306687D1 (de) | 2006-08-17 |
| WO2004024779A2 (en) | 2004-03-25 |
| TW200422310A (en) | 2004-11-01 |
| PL375599A1 (en) | 2005-12-12 |
| BR0314242B1 (pt) | 2014-01-21 |
| BR0314242A (pt) | 2005-07-26 |
| WO2004024779A3 (en) | 2005-08-11 |
| EP1581568B1 (en) | 2006-07-05 |
| JP4482452B2 (ja) | 2010-06-16 |
| JP2006512425A (ja) | 2006-04-13 |
| EP1581568A2 (en) | 2005-10-05 |
| AU2003265662C1 (en) | 2010-10-07 |
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