AU5648800A - Aerosol device containing a hair composition comprising at least one silicone/acrylate copolymer - Google Patents
Aerosol device containing a hair composition comprising at least one silicone/acrylate copolymer Download PDFInfo
- Publication number
- AU5648800A AU5648800A AU56488/00A AU5648800A AU5648800A AU 5648800 A AU5648800 A AU 5648800A AU 56488/00 A AU56488/00 A AU 56488/00A AU 5648800 A AU5648800 A AU 5648800A AU 5648800 A AU5648800 A AU 5648800A
- Authority
- AU
- Australia
- Prior art keywords
- chosen
- groups
- propellant
- acrylate
- silicone
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims description 35
- 229920001296 polysiloxane Polymers 0.000 title claims description 24
- 239000000443 aerosol Substances 0.000 title claims description 21
- 229920001577 copolymer Polymers 0.000 title claims description 19
- 210000004209 hair Anatomy 0.000 title claims description 15
- -1 N,N-dimethylaminoethyl Chemical group 0.000 claims description 39
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 claims description 24
- 239000003380 propellant Substances 0.000 claims description 18
- 239000000178 monomer Substances 0.000 claims description 16
- 229930195733 hydrocarbon Natural products 0.000 claims description 15
- 150000002430 hydrocarbons Chemical class 0.000 claims description 15
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 claims description 10
- 239000002537 cosmetic Substances 0.000 claims description 10
- 229920000642 polymer Polymers 0.000 claims description 10
- 125000000217 alkyl group Chemical group 0.000 claims description 9
- 239000000463 material Substances 0.000 claims description 9
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical class C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 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 7
- 239000004215 Carbon black (E152) Substances 0.000 claims description 7
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 7
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 7
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims description 6
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 claims description 6
- 239000002253 acid Substances 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 6
- 239000012530 fluid Substances 0.000 claims description 6
- 239000001257 hydrogen Substances 0.000 claims description 6
- 229910052739 hydrogen Inorganic materials 0.000 claims description 6
- 238000000034 method Methods 0.000 claims description 6
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 claims description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 6
- 229920002554 vinyl polymer Polymers 0.000 claims description 6
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 claims description 5
- 125000000129 anionic group Chemical group 0.000 claims description 5
- 239000002904 solvent Substances 0.000 claims description 5
- QRIMLDXJAPZHJE-UHFFFAOYSA-N 2,3-dihydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCC(O)CO QRIMLDXJAPZHJE-UHFFFAOYSA-N 0.000 claims description 4
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims description 4
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 claims description 4
- 150000007513 acids Chemical class 0.000 claims description 4
- XXROGKLTLUQVRX-UHFFFAOYSA-N allyl alcohol Chemical compound OCC=C XXROGKLTLUQVRX-UHFFFAOYSA-N 0.000 claims description 4
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 claims description 4
- OWPUOLBODXJOKH-UHFFFAOYSA-N 2,3-dihydroxypropyl prop-2-enoate Chemical compound OCC(O)COC(=O)C=C OWPUOLBODXJOKH-UHFFFAOYSA-N 0.000 claims description 3
- OEPOKWHJYJXUGD-UHFFFAOYSA-N 2-(3-phenylmethoxyphenyl)-1,3-thiazole-4-carbaldehyde Chemical compound O=CC1=CSC(C=2C=C(OCC=3C=CC=CC=3)C=CC=2)=N1 OEPOKWHJYJXUGD-UHFFFAOYSA-N 0.000 claims description 3
- WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical compound CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 claims description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 3
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 3
- 239000000654 additive Substances 0.000 claims description 3
- 230000000996 additive effect Effects 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 239000003795 chemical substances by application Substances 0.000 claims description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 claims description 3
- 235000013870 dimethyl polysiloxane Nutrition 0.000 claims description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 3
- 239000011707 mineral Substances 0.000 claims description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 claims description 3
- 229920001515 polyalkylene glycol Polymers 0.000 claims description 3
- 229920000570 polyether Polymers 0.000 claims description 3
- 238000006116 polymerization reaction Methods 0.000 claims description 3
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 claims description 3
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 claims description 2
- BQBSIHIZDSHADD-UHFFFAOYSA-N 2-ethenyl-4,5-dihydro-1,3-oxazole Chemical compound C=CC1=NCCO1 BQBSIHIZDSHADD-UHFFFAOYSA-N 0.000 claims description 2
- QQBUHYQVKJQAOB-UHFFFAOYSA-N 2-ethenylfuran Chemical compound C=CC1=CC=CO1 QQBUHYQVKJQAOB-UHFFFAOYSA-N 0.000 claims description 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 2
- 125000004200 2-methoxyethyl group Chemical group [H]C([H])([H])OC([H])([H])C([H])([H])* 0.000 claims description 2
- HFCUBKYHMMPGBY-UHFFFAOYSA-N 2-methoxyethyl prop-2-enoate Chemical compound COCCOC(=O)C=C HFCUBKYHMMPGBY-UHFFFAOYSA-N 0.000 claims description 2
- MXRGSJAOLKBZLU-UHFFFAOYSA-N 3-ethenylazepan-2-one Chemical group C=CC1CCCCNC1=O MXRGSJAOLKBZLU-UHFFFAOYSA-N 0.000 claims description 2
- GNSFRPWPOGYVLO-UHFFFAOYSA-N 3-hydroxypropyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OCCCO GNSFRPWPOGYVLO-UHFFFAOYSA-N 0.000 claims description 2
- QZPSOSOOLFHYRR-UHFFFAOYSA-N 3-hydroxypropyl prop-2-enoate Chemical compound OCCCOC(=O)C=C QZPSOSOOLFHYRR-UHFFFAOYSA-N 0.000 claims description 2
- NUXLDNTZFXDNBA-UHFFFAOYSA-N 6-bromo-2-methyl-4h-1,4-benzoxazin-3-one Chemical compound C1=C(Br)C=C2NC(=O)C(C)OC2=C1 NUXLDNTZFXDNBA-UHFFFAOYSA-N 0.000 claims description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 2
- WOBHKFSMXKNTIM-UHFFFAOYSA-N Hydroxyethyl methacrylate Chemical compound CC(=C)C(=O)OCCO WOBHKFSMXKNTIM-UHFFFAOYSA-N 0.000 claims description 2
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical group C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 2
- 150000001252 acrylic acid derivatives Chemical class 0.000 claims description 2
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 claims description 2
- 125000003545 alkoxy group Chemical group 0.000 claims description 2
- 125000005210 alkyl ammonium group Chemical group 0.000 claims description 2
- 239000002280 amphoteric surfactant Substances 0.000 claims description 2
- 239000003945 anionic surfactant Substances 0.000 claims description 2
- 150000001735 carboxylic acids Chemical class 0.000 claims description 2
- 125000002091 cationic group Chemical group 0.000 claims description 2
- 239000003093 cationic surfactant Substances 0.000 claims description 2
- 150000001768 cations Chemical class 0.000 claims description 2
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 claims description 2
- GTBGXKPAKVYEKJ-UHFFFAOYSA-N decyl 2-methylprop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C(C)=C GTBGXKPAKVYEKJ-UHFFFAOYSA-N 0.000 claims description 2
- FWLDHHJLVGRRHD-UHFFFAOYSA-N decyl prop-2-enoate Chemical compound CCCCCCCCCCOC(=O)C=C FWLDHHJLVGRRHD-UHFFFAOYSA-N 0.000 claims description 2
- 125000005131 dialkylammonium group Chemical group 0.000 claims description 2
- 229940008099 dimethicone Drugs 0.000 claims description 2
- UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical compound NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 claims description 2
- 125000006232 ethoxy propyl group Chemical group [H]C([H])([H])C([H])([H])OC([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 210000004709 eyebrow Anatomy 0.000 claims description 2
- 210000000720 eyelash Anatomy 0.000 claims description 2
- 239000003205 fragrance Substances 0.000 claims description 2
- 239000001530 fumaric acid Substances 0.000 claims description 2
- 150000002391 heterocyclic compounds Chemical group 0.000 claims description 2
- 239000007791 liquid phase Substances 0.000 claims description 2
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 claims description 2
- 239000011976 maleic acid Substances 0.000 claims description 2
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 2
- 230000001404 mediated effect Effects 0.000 claims description 2
- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 2
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 claims description 2
- 229940088644 n,n-dimethylacrylamide Drugs 0.000 claims description 2
- YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 claims description 2
- ZQXSMRAEXCEDJD-UHFFFAOYSA-N n-ethenylformamide Chemical compound C=CNC=O ZQXSMRAEXCEDJD-UHFFFAOYSA-N 0.000 claims description 2
- ZIWDVJPPVMGJGR-UHFFFAOYSA-N n-ethyl-2-methylprop-2-enamide Chemical compound CCNC(=O)C(C)=C ZIWDVJPPVMGJGR-UHFFFAOYSA-N 0.000 claims description 2
- SWPMNMYLORDLJE-UHFFFAOYSA-N n-ethylprop-2-enamide Chemical compound CCNC(=O)C=C SWPMNMYLORDLJE-UHFFFAOYSA-N 0.000 claims description 2
- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 239000003921 oil Substances 0.000 claims description 2
- 125000005702 oxyalkylene group Chemical group 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 2
- 102000004169 proteins and genes Human genes 0.000 claims description 2
- 108090000623 proteins and genes Proteins 0.000 claims description 2
- 238000012216 screening Methods 0.000 claims description 2
- 238000007493 shaping process Methods 0.000 claims description 2
- 239000004094 surface-active agent Substances 0.000 claims description 2
- 125000005207 tetraalkylammonium group Chemical group 0.000 claims description 2
- 125000005208 trialkylammonium group Chemical group 0.000 claims description 2
- 239000011782 vitamin Substances 0.000 claims description 2
- 229940088594 vitamin Drugs 0.000 claims description 2
- 229930003231 vitamin Natural products 0.000 claims description 2
- 235000013343 vitamin Nutrition 0.000 claims description 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims 3
- 101100516572 Caenorhabditis elegans nhr-8 gene Proteins 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 9
- 150000003254 radicals Chemical class 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 150000001298 alcohols Chemical class 0.000 description 3
- 125000003118 aryl group Chemical group 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 238000006386 neutralization reaction Methods 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- OFBQJSOFQDEBGM-UHFFFAOYSA-N Pentane Chemical compound CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- 150000001408 amides Chemical class 0.000 description 2
- 150000001414 amino alcohols Chemical class 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 238000000227 grinding Methods 0.000 description 2
- 150000002431 hydrogen Chemical class 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- 125000000896 monocarboxylic acid group Chemical group 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 2
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 description 1
- KAIHOCOWYAMXQY-OWOJBTEDSA-N (e)-3-cyanoprop-2-enoic acid Chemical compound OC(=O)\C=C\C#N KAIHOCOWYAMXQY-OWOJBTEDSA-N 0.000 description 1
- ZWVMLYRJXORSEP-UHFFFAOYSA-N 1,2,6-Hexanetriol Chemical compound OCCCCC(O)CO ZWVMLYRJXORSEP-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- 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 1
- 239000004925 Acrylic resin Substances 0.000 description 1
- 229920000178 Acrylic resin Polymers 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Chemical group CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 239000004721 Polyphenylene oxide Substances 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 229920004482 WACKER® Polymers 0.000 description 1
- 239000011149 active material Substances 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 230000001476 alcoholic effect Effects 0.000 description 1
- 125000003282 alkyl amino group Chemical group 0.000 description 1
- 125000003368 amide group Chemical group 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 1
- 230000001680 brushing effect Effects 0.000 description 1
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 1
- 125000002704 decyl 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])* 0.000 description 1
- 150000004985 diamines Chemical class 0.000 description 1
- 238000009792 diffusion process Methods 0.000 description 1
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 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 1
- IDGUHHHQCWSQLU-UHFFFAOYSA-N ethanol;hydrate Chemical compound O.CCO IDGUHHHQCWSQLU-UHFFFAOYSA-N 0.000 description 1
- 125000001153 fluoro group Chemical group F* 0.000 description 1
- 239000007789 gas Substances 0.000 description 1
- 150000005826 halohydrocarbons Chemical class 0.000 description 1
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 229940051250 hexylene glycol Drugs 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 239000001282 iso-butane Substances 0.000 description 1
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- 150000002734 metacrylic acid derivatives Chemical class 0.000 description 1
- XMYQHJDBLRZMLW-UHFFFAOYSA-N methanolamine Chemical compound NCO XMYQHJDBLRZMLW-UHFFFAOYSA-N 0.000 description 1
- 229940087646 methanolamine Drugs 0.000 description 1
- VHWYCFISAQVCCP-UHFFFAOYSA-N methoxymethanol Chemical compound COCO VHWYCFISAQVCCP-UHFFFAOYSA-N 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- 125000001624 naphthyl group Chemical group 0.000 description 1
- 229910052757 nitrogen Inorganic materials 0.000 description 1
- 125000004433 nitrogen atom Chemical group N* 0.000 description 1
- CXQXSVUQTKDNFP-UHFFFAOYSA-N octamethyltrisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)O[Si](C)(C)C CXQXSVUQTKDNFP-UHFFFAOYSA-N 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- 150000007530 organic bases Chemical class 0.000 description 1
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 238000004987 plasma desorption mass spectroscopy Methods 0.000 description 1
- 239000002952 polymeric resin Substances 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 150000003077 polyols Chemical class 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 229910052710 silicon Inorganic materials 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 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 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229920003002 synthetic resin Polymers 0.000 description 1
- 125000004149 thio group Chemical group *S* 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
Classifications
-
- 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
-
- 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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/891—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone
- A61K8/894—Polysiloxanes saturated, e.g. dimethicone, phenyl trimethicone, C24-C28 methicone or stearyl dimethicone modified by a polyoxyalkylene group, e.g. cetyl dimethicone copolyol
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/02—Cosmetics or similar toiletry preparations characterised by special physical form
- A61K8/04—Dispersions; Emulsions
- A61K8/046—Aerosols; Foams
-
- 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
- A61K8/84—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
- A61K8/89—Polysiloxanes
- A61K8/895—Polysiloxanes containing silicon bound to unsaturated aliphatic groups, e.g. vinyl dimethicone
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Epidemiology (AREA)
- Birds (AREA)
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Cosmetics (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Graft Or Block Polymers (AREA)
Description
AUSTRALIA
Patents Act 1990 COMPLETE SPECIFICATION STANDARD PATENT Applicant(s)
L'OREAL
Invention Title: AEROSOL DEVICE CONTAINING A HAIR COMPOSITION COMPRISING AT LEAST ONE SILICONE/ACRYLATE COPOLYMER The following statement is a full description of this invention, including the best method of performing it known to me/us: I. IH 1A AEROSOL DEVICE CONTAINING A HAIR COMPOSITION COMPRISING AT LEAST ONE SILICONE/ACRYLATE COPOLYMER The invention relates to an aerosol device containing a cosmetic hair composition comprising at least one specific silicone/acrylate copolymer. The invention also relates to a cosmetic hair process, in particular a process for fixing and/or holding the hairstyle by using this aerosol device.
Among hair products for shaping and/or holding the hairstyle which are most widely available on the cosmetics market, there may be mentioned the spray compositions essentially consisting of a oo solution, usually an alcoholic or aqueous solution, and 15 one or more materials, generally polymeric resins, whose function is to form welds between the hairs, and these are also known as fixing materials, mixed with various cosmetic adjuvants. This solution is generally packaged either in a suitable aerosol container placed under pressure with the aid of a propellant, or in a pump-dispenser bottle.
The fixing materials are generally fixing polymers, i.e. film-forming polymers which are soluble in water and in alcohol, such as polyvinylpyrrolidone, the vinylpyrrolidone/vinyl acetate copolymers described in particular in US patents 3 929 735 and 3 770 683, vinyl acetate/crotonic acid copolymers and anionic or amphoteric acrylic resins. Although these materials 2 allow the fixing effect to be obtained easily, after brushing or combing, hair under the usual lacquer conditions has a stiffened appearance and a coarse or even sticky feel, as well as a powdering after drying.
These drawbacks are associated with several parameters, among which may be mentioned the nature of the fixing polymer(s) or the nature of the welds. To overcome these drawbacks, it is thus possible to act on these two parameters without, however, reducing the desired fixing effect. To improve the cosmetic properties of fixing materials, it has especially been .proposed to combine different polymers (WO 94/12148, 96/06592, US 5 158 762) The Applicant has now found that by suitably 15 selecting the fixing polymer and the propellent gas, it is possible to overcome the various problems listed above, and in particular to obtain a spray of good quality in terms of droplet size and diffusion, satisfactory cosmetic properties and little powdering.
One subject of the invention is an aerosol device consisting of a container containing an aerosol composition consisting, on the one hand, of a liquid phase (or fluid) containing at least one fixing material in a suitable solvent, and, on the other hand, of a propellant, and a means for distributing the said aerosol composition, characterized in that: the fixing material is a silicone/acrylate copolymer obtained by radical- 3 mediated polymerization of at least one ethylenically unsaturated monomer in the presence of at least one silicone derivative comprising oxyalkylene groups, and (ii) the propellant is chosen from dimethyl ether, C3-C4 hydrocarbons, mixtures of dimethyl ether and of C3-C5 hydrocarbons and mixtures of C3-C4 hydrocarbons, and (iii) the aerosol composition contains more than 10% water, when the propellant is dimethyl ether alone.
Another subject of the invention relates to a cosmetic hair process, in particular a process for fixing and/or holding the hairstyle using the aerosol 15 device.
The silicone/acrylate copolymers particularly targeted by the present invention are those described in International patent application WO 99/04750. In particular, the copolymer sold by BASF under the name Luviflex Silk is preferred. This polymer is a grafted copolymer of tert-butyl acrylate/methacrylic acid and silicone copolyol.
Preferably, the monomer corresponds to formula (Ia): X-C-CR7=CHR 6 (Ia)
O
in which: X is chosen from the group comprising OH, OM, OR 8
NH
2
NHR
8 and N(R )2; M is a cation chosen from Na Mg", NH 4 alkylammonium, dialkylammonium, trialkylammonium and tetraalkylammonium; the radicals R 8 may be identical or different and-are chosen from the group comprising hydrogen, linear or branched Ci to C 40 alkyl groups, mono- or polyhydroxylated Ci to C 40 alkyl groups, optionally substituted with one or more alkoxy, amino or carboxyl groups, hydroxylated polyethers, and N,N-dimethylaminoethyl, 2-hydroxyethyl, 2-methoxyethyl, 2-ethoxyethyl, hydroxypropyl, methoxypropyl and 15 ethoxypropyl groups; R and R 6 are chosen, independently of each
S
other, from the group comprising hydrogen, linear or branched C 1 to C 8 alkyl groups, methoxy, ethoxy, 2-hydroxyethoxy, 2-methoxyethoxy and 2-ethoxyethyl groups, and CN, COOH and COOM groups.
In particular, the monomers of formula (Ia) are acrylic acid and its salts, esters or amides.
The esters may be derivatives of linear C 1 to C 40 alkyls, of branched C 3 to C 40 alkyls or of C 3 to C 40 carboxylic alcohols, of polyfunctional alcohols containing 2 to 8 hydroxyls, such as ethylene glycol, hexylene glycol, glycerol and 1,2,6-hexanetriol, of amino alcohols or of alcohol ethers such as methoxymethanol and ethoxyethanol, or polyalkylene glycols.
The monomers of formula (Ia) may also be chosen from N,N-dialkylaminoalkyl acrylates and methacrylates and N-dialkylaminoalkyl-acrylamides and -methacrylamides, the amide group possibly being unsubstituted, N-alkyl- or N-alkylamino-monosubstituted or N,N-dialkylamino-disubstituted, the alkyl or alkylamino groups being derived from linear Ci to C 40 or branched C 3 to C 40 carboxylic units.
The monomers of formula (Ia) which can be used may also be substituted compounds derived from acrylic acid or its salts, esters or amides. Mention may be made, for example, of methacrylic acid, 15 ethacrylic acid and 3-cyanoacrylic acid.
Other monomers which are particularly *99 suitable are C 1 to C 40 vinyl and allyl esters, linear C 3 to C 40 carboxylic acids or C 3 to C 40 carboxycyclic acids, vinyl or allyl haldides, vinyllactams, preferably vinylpyrrolidone and vinylcaprolactam, heterocyclic compounds substituted with vinyl or allyl groups, preferably vinylpyridine, vinyloxazoline and allylpyridine, N-vinylimidazoles, diallylamines, vinylidene chloride, carbon-based unsaturated compounds, such as styrene or isoprene, and acrylic or methacrylic acid derivatives quaternized with epichlorohydrin.
Other monomers which may finally be mentioned are N-vinylimidazoles, diallylamines, vinylidene chloride, carbon-based unsaturated compounds such as styrene and isoprene, and acrylic or methacrylic acid derivatives quaternized with epichlorohydrin.
Monomers which are most particularly preferred are acrylic, methacrylic and ethacrylic acid; methyl, ethyl, propyl, n-butyl, isobutyl, t-butyl, 2-thylhexyl and decyl acrylate; methyl, ethyl, propyl, n-butyl, isobutyl, t-butyl, 2-ethylhexyl and decyl methacrylate; methyl, ethyl, propyl, n-butyl, isobutyl, t-butyl, 2-ethylhexyl and decyl ethacrylate; 2,3-ihydroxypropyl acrylate; 2,3-dihydroxypropyl methacrylate; 2-dihydroxyethyl acrylate; hydroxypropyl acrylate; 2-hydroxyethyl methacrylate; 2-hydroxyethyl ethacrylate; 2-methoxyethyl acrylate; 2-ethoxyethyl methacrylate; 2-ethoxyethyl ethacrylate; hydroxypropyl methacrylate; glyceryl monoacrylate; glyceryl monomethacrylate; polyalkylene glycol (meth)acrylates, unsaturated sulphonic acids, acrylamide, methacrylamide, ethacrylanide, N, N-dimethylacrylamide, N-ethylacrylamide, N-ethylmethacrylamide, 1-vinylimidazole, N,N-dimethylaminoethyl (meth)acrylate, maleic acid, fumaric acid, maleic anhydride and its monoesters, crotonic acid, itaconic acid, vinyl ethers, vinylformamide, vinylamine, vinylpyridine, vinylimidazole, vinylfuran, styrene, styryl sulphonate and allyl alcohol, and mixtures thereof.
The monomer can also contain silicon or fluorine atoms or alternatively thio groups. The monomers can be neutralized if they contain acid groups, this being carried out before or after the polymerization, and partially or totally, so as to adjust the solubility or the degree of dispersion in water to the desired level. Agents serving for the neutralization which may be used are mineral bases, such as sodium carbonate, and organic bases such as amino alcohols, for instance alkanolamines such as methanolamine, 2 -amino-2-methyl-l-propanol or -b triethanolamine, and diamines such as lysine.
15 The monomers can also be quaternized when they contain a basic nitrogen atom. If they contain at least two ethylenic double bonds, the monomers can be partially crosslinked.
The silicone derivatives are in *4* particular the compounds known under the INCI name of dimethicone copolyols or silicone surfactants. Mention may be made of those sold under the brand names Abil® by Goldschmidt, Alkasil® by Rh6ne-Poulenc, silicone Polyol Copolymer® by Genesee, Besil® by Wacker, Silwet® by OSI or Dow Corning 190® by Dow Corning.
Among the preferred silicone derivatives(b) are those which have the formula I below: 8 in which formula R 2 is chosen from CH 3 and the group 5 R 3 is chosen from CH 3 and the group R2 R 4 is chosen from hydrogen,
CH
3 and the groups $1 GH 3 *F R Ro 6 is an organic C to C 40 group which can contain amino, carboxyl or suiphonate groups, and if c=O, R 6 is the anion of an inorganic acid; the radicals R 1 may be identical or different and are chosen from C 1 to C 20 aliphatic hydrocarbons,
C
3 to C 20 aliphatic or cycloaliphatic hydrocarbons, and the groups R 5 corresponding to the formula below: S= -(cH oL 0 n is an integer between 1 and 6, x and y are integers chosen such that the molecular weight of the polysiloxane is between 300 and 30,000, a and b are integers between 0 and 50, and c is 0 or 1.
1
R
1 is preferably chosen from methyl, ethyl, 10 propyl, butyl, isobutyl, pentyl, isopentyl, hexyl, o* octyl, decyl, dodecyl and octadecyl groups, cycloaliphatic radicals, in particular cyclohexyl groups, aromatic groups, in particular phenyl or naphthyl groups, and mixtures of aromatic and aliphatic 15 radicals, such as benzyl and phenylethyl, and also tolyl and xylyl.
The preferred radicals R 4 are those having the formula -(CO)c-R 6
R
6 being an alkyl, cycloalkyl or aryl containing 1 to 4 carbon atoms which can contain additional groups such as NH 2 COOH and/or S03H.
The preferred radicals R 6 are those for which c=0, which are phosphates or sulphates.
The silicone derivatives which are particularly preferred are those having the general formula below: y i- Si--H The relative proportion of derivative in the copolymer is generally from 0.1% to 50% and preferably from 1% to 20% by weight.
The preferred copolymers are the watersoluble silicone/acrylate copolymers or those whose dispersibility in water is such that, in a water/ethanol mixture dosed at 50/50 by volume, they are soluble in a proportion of greater than 0.1 g/1 and preferably greater than 0.2 g/l. Advantageously, the composition according to the invention comprises, as a relative percentage by weight, from 0.1% to 20% of silicone/acrylate copolymer and more preferably from to 10% of this copolymer. The aerosol device advantageously comprises from 10% to 90% of propellant and preferably from 20% to According to a first advantageous embodiment of the device in accordance with the invention, the propellant is dimethyl ether, and this propellant is advantageously present in the aerosol device at a concentration ranging from 30% to According to a second advantageous embodiment of the device in accordance with the invention, the propellant is a C3 to C4 hydrocarbon, and this 11 propellant is advantageously present in the aerosol device at a concentration ranging from 10% to 70%. The hydrocarbon is preferably chosen from n-butane, propane, isobutane and halohydrocarbons, and mixtures thereof.
According to a third advantageous embodiment of the device in accordance with the invention, the propellant is a mixture of dimethyl ether and of C3 to hydrocarbon(s), and the dimethyl 10 ether/hydrocarbon(s) ratio is advantageously between 90 and 90 The cosmetically acceptable medium preferably ••go consists of water or one or more cosmetically acceptable solvents or water/solvent mixtures. These 15 solvents are preferably Cl-C4 alcohols, ethanol being e particularly preferred.
The appropriate solvent advantageously contains at least 50% by volume of alcohol, preferably at least 70% by volume of alcohol.
The composition of the invention can also contain at least one additive chosen from anionic, cationic, nonionic and amphoteric surfactants, fragrances, screening agents, preserving agents, proteins, vitamins, polymers other than those of the invention, and in particular anionic, amphoteric or nonionic fixing polymers, plant, mineral or synthetic oils and any other additive conventionally used in cosmetic compositions.
Needless to say, a person skilled in the art will take care to select the optional compound(s) to be added to the composition according to the invention such that the advantageous properties intrinsically associated with the composition in accordance with the invention are not, or are not substantially, adversely affected by the addition envisaged.
The compositions in accordance with the invention are particularly suitable for dry or wet hair, as styling products.
The compositions in accordance with the invention can be applied to the skin, the nails, the lips, the hair, the eyebrows and the eyelashes.
The invention will be illustrated more fully with the aid of the non-limiting examples which follow.
All the percentages are relative percentages by weight with respect to the total weight of the composition, and a.m. means active material.
20 EXAMPLE: The aerosol device below in accordance with the invention is prepared.
Composition A Fluid: Luviflex Silk* 6%
AMP
Ethanol qs 100% neutralization qs 100 g Pressurization scheme: Fluid
DME
Pentane 37% 43% Composition B Fluid: Luviflex Silk* Amphomer LV 71
AMP
Water Ethanol 4% 2% qs 100% neutralization 16% 78% Pressurization scheme: Fluid
DME
These two compositions are individually sprayed on European chestnut-brown hair. The hair has good cosmetic properties in both cases, after drying.
14 silicone/acrylate copolymer sold by BASF (t-butyl acrylate/methacrylic acid/PDMS polyether) It is to be understood that, if any prior art publication is referred to herein, such reference does not constitute an admission that the publication forms a part of the common general knowledge in the art, in Australia or any other country.
For the purposes of this specification it will be clearly understood that the word "comprising" means "including but not limited to", and that the word "comprises" has a corresponding meaning.
go*
Claims (13)
1. Aerosol device consisting of a container containing an aerosol composition consisting, on the one hand, of a liquid phase (or fluid) containing at least one fixing material in a suitable solvent, and, on the other hand, of a propellant, and a means for distributing the said aerosol composition, characterized in that: 10 the fixing material is a silicone/acrylate copolymer obtained by radical- mediated polymerization of at least one ethylenically unsaturated monomer in the presence of at least one silicone derivative comprising oxyalkylene groups, 15 and (ii) the propellant is chosen from dimethyl ether, C3-C4 hydrocarbons, mixtures of dimethyl ether and of C3-C5 hydrocarbons and mixtures of C3-C4 hydrocarbons, and (iii) the aerosol composition contains more than 10% water, when the propellant is dimethyl ether alone.
2. Device according to Claim 1, characterized in that the monomer corresponds to formula (Ia): X-C-CR7=CHR 6 (Ia) O in which: X is chosen from the group comprising OH, OM, OR 8 NH 2 NHR 8 and N(R 8 2 M is a cation chosen from Na', K Mg*, NH 4 alkylammonium, dialkylammonium, trialkylammonium and tetraalkylammonium; the radicals R 8 may be identical or different and are chosen from the group comprising hydrogen, linear or branched C 1 to C 40 alkyl groups, 1 0 mono- or polyhydroxylated C 1 to C 40 alkyl groups, optionally substituted with one or more alkoxy, amino or carboxyl groups, hydroxylated polyethers, and N,N-dimethylaminoethyl, 2-hydroxyethyl, 2-methoxyethyl, 2-ethoxyethyl, hydroxypropyl, methoxypropyl and ethoxypropyl groups; R 7 and R 6 are chosen, independently of each other, from the group comprising hydrogen, linear or branched Ci to C 8 alkyl groups, methoxy, ethoxy, 2-hydroxyethoxy, 2-methoxyethoxy and 2-ethoxyethyl groups, and CN, COOH and COOM groups.
3. Device according to Claim 1, characterized in that the silicone derivative (b) corresponds to the formula below: 8 -I FLA in which formula R 2 is chosen from CH 3 and the group R R 3 is chosen from CH 3 and the group R 2 R 4 is chosen from hydrogen, CH 3 and the groups 1 1 L J 11 ^m hydrocarbn is an organic C to C 40 group which can contain amino, carboxyl or suphonate groups, and if 9 c=0 Rssth an ofrg iranic acid;0gru wih a 151 1oo 0 the radicals R I may be identical or different and are chosen from C 1 to C 20 aliphatic hydrocarbons, C 3 to C 20 aliphatic or cycloaliphatic hydrocarbons, and the groups R 5 corresponding to the formula below: R OPjb R n. is an integer between 1 and 6, 18 x and y are integers chosen such that the molecular weight of the polysiloxane is between 300 and 30,000, a and b are integers between 0 and 50, and c is 0 or 1.
4. Device according to Claim 1, characterized in that the monomer is chosen from C 1 to C40 vinyl and allyl esters, linear C3 to carboxylic acids or C3 to C40 carboxycyclic acids, vinyl .1 0 or allyl haldides, vinyllactams, preferably vinylpyrrolidone and vinylcaprolactam, heterocyclic compounds substituted with vinyl or allyl groups, preferably vinylpyridine, vinyloxazoline and allylpyridine, N-vinylimidazoles, diallylamines, ooo 15 vinylidene chloride, carbon-based unsaturated compounds, such as styrene or isoprene, and acrylic or methacrylic acid derivatives quaternized with epichlorohydrin.
5. Device according to Claim 1, characterized in that the monomer is chosen from the group comprising acrylic, methacrylic and ethacrylic acid; methyl, ethyl, propyl, n-butyl, isobutyl, t-butyl, 2-ethylhexyl and decyl acrylate; methyl, ethyl, propyl, n-butyl, isobutyl, t-butyl, 2-ethylhexyl and decyl methacrylate; methyl, ethyl, propyl, n-butyl, isobutyl, t-butyl, 2-ethylhexyl and decyl ethacrylate; 2,3-dihydroxypropyl acrylate; 2,3-dihydroxypropyl methacrylate; 2-dihydroxyethyl 19 acrylate; hydroxypropyl acrylate; 2-hydroxyethyl methacrylate; 2-hydroxyethyl ethacrylate; 2-methoxyethyl acrylate; 2-ethoxyethyl methacrylate; 2-ethoxyethyl ethacrylate; hydroxypropyl methacrylate; glyceryl monoacrylate; glyceryl monomethacrylate; polyalkylene glycol (meth)acrylates, unsaturated sulphonic acids, acrylamide, methacrylamide, ethacrylamide, N,N-dimethylacrylamide, N-ethyl- acrylamide, N-ethylmethacrylamide, 1-vinylimidazole, 10 N,N-dimethylaminoethyl (meth)acrylate, maleic acid, fumaric acid, maleic anhydride and its monoesters, crotonic acid, itaconic acid, vinyl ethers, vinylformamide, vinylamine, vinylpyridine, vinylimidazole, vinylfuran, styrene, styryl sulphonate 15 and allyl alcohol, and mixtures thereof.
6. Device according to any one of the Spreceding claims, characterized in that the silicone derivatives are chosen from dimethicone copolyols and silicone surfactants.
7. Device according to any one of the preceding claims, characterized in that it comprises, as a relative percentage by weight, from 0.1% to 20% of silicone/acrylate copolymer, and more preferably from to 10% of this copolymer.
8. Device according to any one of the preceding claims, characterized in that the propellant is dimethyl ether, and this propellant is advantageously present in the aerosol device at a concentration ranging from 30% to
9. Device according to any one of Claims 1 to 7, characterized in that the propellant is a C3 to C4 hydrocarbon, and this propellant is present in the aerosol device at a concentration ranging from 10% to Device according to any one of Claims 1 to 7, characterized in that the propellant is a mixture 10 of dimethyl ether and of C3 to C5 hydrocarbon(s), and *"the dimethyl ether/hydrocarbon(s) ratio is between 90 and 90
11. Device according to any one of the preceding claims, characterized in that the composition 15 also contains at least one additive chosen from anionic, cationic, nonionic and amphoteric surfactants, fragrances, screening agents, preserving agents, *e proteins, vitamins, polymers other than those of the invention, and in particular anionic, amphoteric or nonionic fixing polymers, and plant, mineral or synthetic oils.
12. Process for holding or shaping the hairstyle, characterized in that it uses a device in accordance with any one of Claims 1 to 11.
13. Use of a device according to any one of Claims 1 to 11, for the manufacture of a cosmetic product, in particular a hair product. 0 1. 21
14. Use of a composition according to any one of Claims 1 to 11, for the skin, the nails, the lips, the hair, the eyebrows and the eyelashes. Dated this 5th day of September 2000 L 'OREAL By their Patent Attorneys GRIFFITH HACK Fellows Institute of Patent and Trade Mark Attorneys of Australia se S 669:0 se 0 0
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9911595 | 1999-09-16 | ||
FR9911595A FR2798588B1 (en) | 1999-09-16 | 1999-09-16 | AEROSOL DEVICE CONTAINING A HAIR COMPOSITION COMPRISING AT LEAST ONE SILICONE / ACRYLATE COPOLYMER |
Publications (2)
Publication Number | Publication Date |
---|---|
AU5648800A true AU5648800A (en) | 2001-03-22 |
AU748685B2 AU748685B2 (en) | 2002-06-13 |
Family
ID=9549921
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU56488/00A Ceased AU748685B2 (en) | 1999-09-16 | 2000-09-05 | Aerosol device containing a hair composition comprising at least one silicone/acrylate copolymer |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP1084699A1 (en) |
JP (1) | JP2001097810A (en) |
KR (1) | KR20010030417A (en) |
CN (1) | CN1293029A (en) |
AU (1) | AU748685B2 (en) |
BR (1) | BR0004405A (en) |
CA (1) | CA2319947A1 (en) |
FR (1) | FR2798588B1 (en) |
PL (1) | PL342560A1 (en) |
RU (1) | RU2203102C2 (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2968544B1 (en) * | 2010-12-14 | 2013-01-11 | Oreal | PLANE DIFFUSION AEROSOL DEVICE FOR HAIR STAPPING |
FR3017288B1 (en) * | 2014-02-10 | 2019-06-07 | Bbr | COSMETIC COMPOSITION SUITABLE FOR MODIFYING THE COLOR OF KERATIN FIBERS, IN PARTICULAR HAIR |
US20210299026A1 (en) | 2018-07-17 | 2021-09-30 | Lg Chem, Ltd. | Hair styling composition and spray system |
CN110152177A (en) * | 2019-06-17 | 2019-08-23 | 沈昌 | A kind of anion cream and preparation method |
KR20210003693A (en) | 2019-07-02 | 2021-01-12 | 주식회사 엘지생활건강 | Injection system of spray comprising hair styling composition |
FR3109730B1 (en) * | 2020-04-30 | 2023-10-06 | Oreal | Aerosol device containing a composition comprising at least one silicone acrylic copolymer and at least one propellant |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5166276A (en) * | 1989-07-12 | 1992-11-24 | Mitsubishi Petrochemical Company Ltd. | Polymer for hair-care products |
FR2735689B1 (en) * | 1995-06-21 | 1997-08-01 | Oreal | COMPOSITION COMPRISING A DISPERSION OF POLYMER PARTICLES IN A NON-AQUEOUS MEDIUM |
ES2318872T3 (en) * | 1997-07-23 | 2009-05-01 | Basf Se | EMPLOYMENT OF POLYMERS THAT CONTAIN POLYSYLOXANE FOR COSMETIC FORMULATIONS. |
WO2001013884A2 (en) | 1999-08-26 | 2001-03-01 | Basf Aktiengesellschaft | Cosmetic and/or pharmaceutical preparations with polymers containing polysiloxanes and the uses thereof |
-
1999
- 1999-09-16 FR FR9911595A patent/FR2798588B1/en not_active Expired - Fee Related
-
2000
- 2000-08-28 EP EP00402378A patent/EP1084699A1/en not_active Withdrawn
- 2000-09-05 AU AU56488/00A patent/AU748685B2/en not_active Ceased
- 2000-09-12 JP JP2000277132A patent/JP2001097810A/en active Pending
- 2000-09-14 CA CA002319947A patent/CA2319947A1/en not_active Abandoned
- 2000-09-15 PL PL00342560A patent/PL342560A1/en not_active Application Discontinuation
- 2000-09-15 BR BR0004405-9A patent/BR0004405A/en not_active IP Right Cessation
- 2000-09-15 RU RU2000123754/14A patent/RU2203102C2/en not_active IP Right Cessation
- 2000-09-15 CN CN00128742A patent/CN1293029A/en active Pending
- 2000-09-16 KR KR1020000054454A patent/KR20010030417A/en active IP Right Grant
Also Published As
Publication number | Publication date |
---|---|
FR2798588B1 (en) | 2001-11-30 |
EP1084699A1 (en) | 2001-03-21 |
PL342560A1 (en) | 2001-03-26 |
RU2203102C2 (en) | 2003-04-27 |
BR0004405A (en) | 2001-04-10 |
JP2001097810A (en) | 2001-04-10 |
AU748685B2 (en) | 2002-06-13 |
CA2319947A1 (en) | 2001-03-16 |
FR2798588A1 (en) | 2001-03-23 |
KR20010030417A (en) | 2001-04-16 |
CN1293029A (en) | 2001-05-02 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU748211B2 (en) | Cosmetic composition comprising at least one silicone/ acrylate copolymer and at least one thickening agent | |
RU2152781C1 (en) | Aqueous hairspray for treating keratin composition packed in aerosol can and its application | |
JP2004503626A (en) | Branched / block copolymers for the treatment of keratin substrates | |
US6011126A (en) | Topical composition comprising the combination of a polymer with a non-silicone skeleton with silicone grafts and of a polymer with a polysiloxane skeleton with non-silicone grafts | |
JPH0789830A (en) | Fixing power reinforcing agent for composition for keeping hair style and make-up article composition for keeping hair style | |
JP3549897B2 (en) | Composition for the treatment of keratin materials containing a thickening polymer or copolymer of at least one grafted silicone polymer and at least one (meth) acrylamide or (meth) acrylamide derivative and use thereof | |
US20020136699A1 (en) | Cosmetic composition for treating keratin substances, comprising at least one grafted silicone polymer and at least one aqueous dispersion of insoluble particles of nonionic or cationic polymer | |
RU2201197C2 (en) | Composition for hair | |
RU2168325C2 (en) | Cosmetic composition containing at least one silicone graft-polymer and at least one linear block-copolymer of polysiloxane and polyoxyalkylene | |
AU748685B2 (en) | Aerosol device containing a hair composition comprising at least one silicone/acrylate copolymer | |
EP1084694B2 (en) | Cosmetic composition containing at least a silicone/acrylate copolymer and at least a conditioning agent | |
AU750093B2 (en) | Cosmetic composition comprising at least one silicone/ acrylate copolymer and at least one grafted silicone polymer | |
AU748149B2 (en) | Cosmetic composition comprising at least one silicone/ acrylate copolymer and at least one nonionic polymer with a vinyllactam unit |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FGA | Letters patent sealed or granted (standard patent) |