MXPA00010166A - Cosmetic aqueous emulsion composition containing a vinyldimethicone/dimethicone copolymer and a thickener, and their uses - Google Patents
Cosmetic aqueous emulsion composition containing a vinyldimethicone/dimethicone copolymer and a thickener, and their usesInfo
- Publication number
- MXPA00010166A MXPA00010166A MXPA/A/2000/010166A MXPA00010166A MXPA00010166A MX PA00010166 A MXPA00010166 A MX PA00010166A MX PA00010166 A MXPA00010166 A MX PA00010166A MX PA00010166 A MXPA00010166 A MX PA00010166A
- Authority
- MX
- Mexico
- Prior art keywords
- composition according
- weight
- composition
- groups
- polysiloxane
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 99
- 239000000839 emulsion Substances 0.000 title claims abstract description 30
- 239000002562 thickening agent Substances 0.000 title claims abstract description 24
- 239000002537 cosmetic Substances 0.000 title claims abstract description 19
- 239000004205 dimethyl polysiloxane Substances 0.000 title claims description 9
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 title claims description 9
- 235000013870 dimethyl polysiloxane Nutrition 0.000 title description 7
- UQEAIHBTYFGYIE-UHFFFAOYSA-N Hexamethyldisiloxane Chemical compound C[Si](C)(C)O[Si](C)(C)C UQEAIHBTYFGYIE-UHFFFAOYSA-N 0.000 title description 5
- 229940008099 dimethicone Drugs 0.000 title description 5
- -1 polysiloxane Polymers 0.000 claims abstract description 79
- 229920001296 polysiloxane Polymers 0.000 claims abstract description 46
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 17
- 150000001875 compounds Chemical class 0.000 claims abstract description 17
- 239000003054 catalyst Substances 0.000 claims abstract description 7
- 125000001931 aliphatic group Chemical group 0.000 claims abstract description 6
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims abstract description 4
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims abstract description 4
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims abstract description 3
- 125000006038 hexenyl group Chemical group 0.000 claims abstract description 3
- 229920001577 copolymer Polymers 0.000 claims description 31
- 210000004209 Hair Anatomy 0.000 claims description 22
- 125000004432 carbon atoms Chemical group C* 0.000 claims description 20
- HRPVXLWXLXDGHG-UHFFFAOYSA-N acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 13
- 239000011780 sodium chloride Substances 0.000 claims description 13
- 150000003839 salts Chemical class 0.000 claims description 11
- 238000005406 washing Methods 0.000 claims description 11
- 125000004435 hydrogen atoms Chemical group [H]* 0.000 claims description 10
- 150000001412 amines Chemical group 0.000 claims description 9
- 239000004094 surface-active agent Substances 0.000 claims description 9
- 102000011782 Keratins Human genes 0.000 claims description 8
- 108010076876 Keratins Proteins 0.000 claims description 8
- 239000002280 amphoteric surfactant Substances 0.000 claims description 8
- 239000000463 material Substances 0.000 claims description 8
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 8
- 239000003093 cationic surfactant Substances 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid Chemical compound OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims description 6
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 6
- 238000007259 addition reaction Methods 0.000 claims description 5
- 125000000129 anionic group Chemical group 0.000 claims description 5
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 5
- 229920001223 polyethylene glycol Polymers 0.000 claims description 5
- 229920000642 polymer Polymers 0.000 claims description 5
- 150000003871 sulfonates Chemical group 0.000 claims description 5
- 150000003467 sulfuric acid derivatives Chemical group 0.000 claims description 5
- 150000002148 esters Chemical group 0.000 claims description 4
- 239000002245 particle Substances 0.000 claims description 4
- 239000002453 shampoo Substances 0.000 claims description 4
- RRHXZLALVWBDKH-UHFFFAOYSA-M trimethyl-[2-(2-methylprop-2-enoyloxy)ethyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)OCC[N+](C)(C)C RRHXZLALVWBDKH-UHFFFAOYSA-M 0.000 claims description 4
- FQPSGWSUVKBHSU-UHFFFAOYSA-N Methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 3
- 238000004040 coloring Methods 0.000 claims description 3
- 150000002170 ethers Chemical group 0.000 claims description 3
- 229920001519 homopolymer Polymers 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 3
- 229920001285 xanthan gum Polymers 0.000 claims description 3
- 235000013912 Ceratonia siliqua Nutrition 0.000 claims description 2
- 240000008886 Ceratonia siliqua Species 0.000 claims description 2
- 240000005497 Cyamopsis tetragonoloba Species 0.000 claims description 2
- 239000005913 Maltodextrin Substances 0.000 claims description 2
- 229920002774 Maltodextrin Polymers 0.000 claims description 2
- 229920002305 Schizophyllan Polymers 0.000 claims description 2
- FEBUJFMRSBAMES-UHFFFAOYSA-N Scleroglucan Chemical compound OC1C(O)C(O)C(CO)OC1OCC1C(O)C(OC2C(C(OP)C(O)C(CO)O2)O)C(O)C(OC2C(C(CO)OC(P)C2O)O)O1 FEBUJFMRSBAMES-UHFFFAOYSA-N 0.000 claims description 2
- 229920002472 Starch Polymers 0.000 claims description 2
- 229920000615 alginic acid Polymers 0.000 claims description 2
- 235000010443 alginic acid Nutrition 0.000 claims description 2
- 125000003118 aryl group Chemical group 0.000 claims description 2
- 235000013312 flour Nutrition 0.000 claims description 2
- 125000000524 functional group Chemical group 0.000 claims description 2
- 238000006459 hydrosilylation reaction Methods 0.000 claims description 2
- 229940035034 maltodextrin Drugs 0.000 claims description 2
- CERQOIWHTDAKMF-UHFFFAOYSA-N methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
- 229920002401 polyacrylamide Polymers 0.000 claims description 2
- 239000008107 starch Substances 0.000 claims description 2
- 235000019698 starch Nutrition 0.000 claims description 2
- 150000003573 thiols Chemical group 0.000 claims description 2
- XHZPRMZZQOIPDS-UHFFFAOYSA-N 2-Acrylamido-2-methylpropane sulfonic acid Chemical compound OS(=O)(=O)CC(C)(C)NC(=O)C=C XHZPRMZZQOIPDS-UHFFFAOYSA-N 0.000 claims 1
- 229920000536 2-Acrylamido-2-methylpropane sulfonic acid Polymers 0.000 claims 1
- AUZRCMMVHXRSGT-UHFFFAOYSA-N 2-methylpropane-1-sulfonic acid;prop-2-enamide Chemical compound NC(=O)C=C.CC(C)CS(O)(=O)=O AUZRCMMVHXRSGT-UHFFFAOYSA-N 0.000 claims 1
- 229920000569 Gum karaya Polymers 0.000 claims 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N Xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 claims 1
- 150000003926 acrylamides Chemical class 0.000 claims 1
- 238000006243 chemical reaction Methods 0.000 claims 1
- 238000002845 discoloration Methods 0.000 claims 1
- 235000010494 karaya gum Nutrition 0.000 claims 1
- 238000000034 method Methods 0.000 claims 1
- 238000005507 spraying Methods 0.000 claims 1
- QAOWNCQODCNURD-UHFFFAOYSA-L sulfate group Chemical group S(=O)(=O)([O-])[O-] QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 abstract description 2
- 229910003849 O-Si Inorganic materials 0.000 abstract 2
- 229910003872 O—Si Inorganic materials 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 1
- 125000004185 ester group Chemical group 0.000 abstract 1
- 125000001033 ether group Chemical group 0.000 abstract 1
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 abstract 1
- 125000003396 thiol group Chemical group [H]S* 0.000 abstract 1
- 150000003254 radicals Chemical class 0.000 description 12
- 239000003945 anionic surfactant Substances 0.000 description 10
- 239000002253 acid Substances 0.000 description 9
- IAYPIBMASNFSPL-UHFFFAOYSA-N oxane Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 8
- 210000003491 Skin Anatomy 0.000 description 7
- 235000014113 dietary fatty acids Nutrition 0.000 description 7
- 239000000194 fatty acid Substances 0.000 description 7
- 239000002736 nonionic surfactant Substances 0.000 description 6
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 150000001450 anions Chemical group 0.000 description 5
- 125000002091 cationic group Chemical group 0.000 description 5
- 239000006185 dispersion Substances 0.000 description 5
- 239000003921 oil Substances 0.000 description 5
- 235000021317 phosphate Nutrition 0.000 description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 5
- 235000013162 Cocos nucifera Nutrition 0.000 description 4
- 240000007170 Cocos nucifera Species 0.000 description 4
- 239000000654 additive Substances 0.000 description 4
- 239000002585 base Substances 0.000 description 4
- 229910052799 carbon Inorganic materials 0.000 description 4
- VEXZGXHMUGYJMC-UHFFFAOYSA-M chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 4
- 239000003995 emulsifying agent Substances 0.000 description 4
- 150000004665 fatty acids Chemical class 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 229920001888 polyacrylic acid Polymers 0.000 description 4
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 3
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Tris Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 3
- 230000000996 additive Effects 0.000 description 3
- 125000003545 alkoxy group Chemical group 0.000 description 3
- 150000008051 alkyl sulfates Chemical class 0.000 description 3
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 3
- 150000001732 carboxylic acid derivatives Chemical class 0.000 description 3
- 230000003750 conditioning Effects 0.000 description 3
- 239000006260 foam Substances 0.000 description 3
- 238000005187 foaming Methods 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 150000004820 halides Chemical class 0.000 description 3
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 3
- KEAYESYHFKHZAL-UHFFFAOYSA-N sodium Chemical compound [Na] KEAYESYHFKHZAL-UHFFFAOYSA-N 0.000 description 3
- 229910052708 sodium Inorganic materials 0.000 description 3
- 239000011734 sodium Substances 0.000 description 3
- MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-bis(ethenyl)benzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 description 2
- 210000000720 Eyelashes Anatomy 0.000 description 2
- 210000000088 Lip Anatomy 0.000 description 2
- 210000000282 Nails Anatomy 0.000 description 2
- 239000002202 Polyethylene glycol Substances 0.000 description 2
- 229940079053 QUATERNIUM-27 Drugs 0.000 description 2
- QIQXTHQIDYTFRH-UHFFFAOYSA-N Stearic acid Chemical class CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L Sulphite Chemical compound [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 150000001242 acetic acid derivatives Chemical class 0.000 description 2
- 150000007513 acids Chemical class 0.000 description 2
- 239000011149 active material Substances 0.000 description 2
- 125000002252 acyl group Chemical group 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 125000005418 aryl aryl group Chemical group 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 239000000084 colloidal system Substances 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 239000003431 cross linking reagent Substances 0.000 description 2
- 239000003599 detergent Substances 0.000 description 2
- QXNVGIXVLWOKEQ-UHFFFAOYSA-N disodium Chemical compound [Na][Na] QXNVGIXVLWOKEQ-UHFFFAOYSA-N 0.000 description 2
- 150000002193 fatty amides Chemical class 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol group Chemical group OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 229910052736 halogen Inorganic materials 0.000 description 2
- 150000002367 halogens Chemical class 0.000 description 2
- 125000005842 heteroatoms Chemical group 0.000 description 2
- 239000001257 hydrogen Substances 0.000 description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 description 2
- 229910052739 hydrogen Inorganic materials 0.000 description 2
- 239000006210 lotion Substances 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000001301 oxygen Substances 0.000 description 2
- 229910052760 oxygen Inorganic materials 0.000 description 2
- MYMOFIZGZYHOMD-UHFFFAOYSA-N oxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 description 2
- 239000002304 perfume Substances 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 230000002335 preservative Effects 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- FWFUWXVFYKCSQA-UHFFFAOYSA-M sodium;2-methyl-2-(prop-2-enoylamino)propane-1-sulfonate Chemical compound [Na+].[O-]S(=O)(=O)CC(C)(C)NC(=O)C=C FWFUWXVFYKCSQA-UHFFFAOYSA-M 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 229910052717 sulfur Inorganic materials 0.000 description 2
- 239000011593 sulfur Substances 0.000 description 2
- 238000003786 synthesis reaction Methods 0.000 description 2
- 230000002194 synthesizing Effects 0.000 description 2
- 239000003760 tallow Substances 0.000 description 2
- 239000004711 α-olefin Substances 0.000 description 2
- 125000006699 (C1-C3) hydroxyalkyl group Chemical group 0.000 description 1
- CMCBDXRRFKYBDG-UHFFFAOYSA-N 1-dodecoxydodecane Chemical compound CCCCCCCCCCCCOCCCCCCCCCCCC CMCBDXRRFKYBDG-UHFFFAOYSA-N 0.000 description 1
- WSRCOZWDQPJAQT-UHFFFAOYSA-N 18-methylicosanoic acid Chemical compound CCC(C)CCCCCCCCCCCCCCCCC(O)=O WSRCOZWDQPJAQT-UHFFFAOYSA-N 0.000 description 1
- OZAIFHULBGXAKX-UHFFFAOYSA-N 2,2'-azo-bis-isobutyronitrile Substances N#CC(C)(C)N=NC(C)(C)C#N OZAIFHULBGXAKX-UHFFFAOYSA-N 0.000 description 1
- PFHLGQKVKALLMD-UHFFFAOYSA-N 2,2-dimethylhexan-3-ol Chemical compound CCCC(O)C(C)(C)C PFHLGQKVKALLMD-UHFFFAOYSA-N 0.000 description 1
- 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 1
- WECIKJKLCDCIMY-UHFFFAOYSA-N 2-chloro-N-(2-cyanoethyl)acetamide Chemical compound ClCC(=O)NCCC#N WECIKJKLCDCIMY-UHFFFAOYSA-N 0.000 description 1
- LJPCNSSTRWGCMZ-UHFFFAOYSA-N 3-methyloxolane Chemical compound CC1CCOC1 LJPCNSSTRWGCMZ-UHFFFAOYSA-N 0.000 description 1
- ATVJXMYDOSMEPO-UHFFFAOYSA-N 3-prop-2-enoxyprop-1-ene Chemical compound C=CCOCC=C ATVJXMYDOSMEPO-UHFFFAOYSA-N 0.000 description 1
- MTNDZQHUAFNZQY-UHFFFAOYSA-O 4,5-dihydro-1H-imidazol-1-ium Chemical compound C1CN=C[NH2+]1 MTNDZQHUAFNZQY-UHFFFAOYSA-O 0.000 description 1
- CWSZBVAUYPTXTG-UHFFFAOYSA-N 5-[6-[[3,4-dihydroxy-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxymethyl]-3,4-dihydroxy-5-[4-hydroxy-3-(2-hydroxyethoxy)-6-(hydroxymethyl)-5-methoxyoxan-2-yl]oxyoxan-2-yl]oxy-6-(hydroxymethyl)-2-methyloxane-3,4-diol Chemical compound O1C(CO)C(OC)C(O)C(O)C1OCC1C(OC2C(C(O)C(OC)C(CO)O2)OCCO)C(O)C(O)C(OC2C(OC(C)C(O)C2O)CO)O1 CWSZBVAUYPTXTG-UHFFFAOYSA-N 0.000 description 1
- 229940045714 Alkyl sulfonate alkylating agents Drugs 0.000 description 1
- HEBKCHPVOIAQTA-QWWZWVQMSA-N Arabitol Chemical compound OC[C@@H](O)C(O)[C@H](O)CO HEBKCHPVOIAQTA-QWWZWVQMSA-N 0.000 description 1
- OZAIFHULBGXAKX-VAWYXSNFSA-N Azobisisobutyronitrile Chemical compound N#CC(C)(C)\N=N\C(C)(C)C#N OZAIFHULBGXAKX-VAWYXSNFSA-N 0.000 description 1
- YSJGOMATDFSEED-UHFFFAOYSA-M Behentrimonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C YSJGOMATDFSEED-UHFFFAOYSA-M 0.000 description 1
- 229940047648 COCOAMPHODIACETATE Drugs 0.000 description 1
- 229960001631 Carbomer Drugs 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-N Carbonic acid Chemical compound OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 description 1
- 210000004534 Cecum Anatomy 0.000 description 1
- 229940106189 Ceramides Drugs 0.000 description 1
- WOWHHFRSBJGXCM-UHFFFAOYSA-M Cetrimonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N Cetyl alcohol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- NEHMKBQYUWJMIP-UHFFFAOYSA-N Chloromethane Chemical compound ClC NEHMKBQYUWJMIP-UHFFFAOYSA-N 0.000 description 1
- 239000004971 Cross linker Substances 0.000 description 1
- 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 1
- WQZGKKKJIJFFOK-GASJEMHNSA-N D-Glucose Natural products OC[C@H]1OC(O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-GASJEMHNSA-N 0.000 description 1
- FBPFZTCFMRRESA-KAZBKCHUSA-N D-Mannitol Natural products OC[C@@H](O)[C@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KAZBKCHUSA-N 0.000 description 1
- UNXHWFMMPAWVPI-QWWZWVQMSA-N D-Threitol Natural products OC[C@@H](O)[C@H](O)CO UNXHWFMMPAWVPI-QWWZWVQMSA-N 0.000 description 1
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 description 1
- SNPLKNRPJHDVJA-ZETCQYMHSA-N D-panthenol Chemical compound OCC(C)(C)[C@@H](O)C(=O)NCCCO SNPLKNRPJHDVJA-ZETCQYMHSA-N 0.000 description 1
- CZMRCDWAGMRECN-UGDNZRGBSA-N D-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 1
- 229940079857 DISODIUM COCOAMPHODIPROPIONATE Drugs 0.000 description 1
- 229940047642 Disodium Cocoamphodiacetate Drugs 0.000 description 1
- 229940079881 Disodium Lauroamphodiacetate Drugs 0.000 description 1
- 239000004386 Erythritol Substances 0.000 description 1
- UNXHWFMMPAWVPI-ZXZARUISSA-N Erythritol Chemical compound OC[C@H](O)[C@H](O)CO UNXHWFMMPAWVPI-ZXZARUISSA-N 0.000 description 1
- 229940009714 Erythritol Drugs 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- QUPDWYMUPZLYJZ-UHFFFAOYSA-N Ethyl radical Chemical compound C[CH2] QUPDWYMUPZLYJZ-UHFFFAOYSA-N 0.000 description 1
- 210000004709 Eyebrows Anatomy 0.000 description 1
- 229920002148 Gellan gum Polymers 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 241001465754 Metazoa Species 0.000 description 1
- 229940050176 Methyl Chloride Drugs 0.000 description 1
- 210000004080 Milk Anatomy 0.000 description 1
- ZIUHHBKFKCYYJD-UHFFFAOYSA-N N,N'-Methylenebisacrylamide Chemical compound C=CC(=O)NCNC(=O)C=C ZIUHHBKFKCYYJD-UHFFFAOYSA-N 0.000 description 1
- XFHJDMUEHUHAJW-UHFFFAOYSA-N N-tert-butylprop-2-enamide Chemical compound CC(C)(C)NC(=O)C=C XFHJDMUEHUHAJW-UHFFFAOYSA-N 0.000 description 1
- 229940101267 Panthenol Drugs 0.000 description 1
- 239000005662 Paraffin oil Substances 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 210000004761 Scalp Anatomy 0.000 description 1
- 229950011392 Sorbitan stearate Drugs 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- CZMRCDWAGMRECN-GDQSFJPYSA-N Sucrose Natural products O([C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@H](CO)O1)[C@@]1(CO)[C@H](O)[C@@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-GDQSFJPYSA-N 0.000 description 1
- 229940029983 VITAMINS Drugs 0.000 description 1
- ORGHESHFQPYLAO-UHFFFAOYSA-N Vinyl radical Chemical class C=[CH] ORGHESHFQPYLAO-UHFFFAOYSA-N 0.000 description 1
- 229940021016 Vitamin IV solution additives Drugs 0.000 description 1
- HVUMOYIDDBPOLL-IIZJTUPISA-N [2-[(2R,3S,4R)-3,4-dihydroxyoxolan-2-yl]-2-hydroxyethyl] octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)[C@H]1OC[C@@H](O)[C@@H]1O HVUMOYIDDBPOLL-IIZJTUPISA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000008055 alkyl aryl sulfonates Chemical class 0.000 description 1
- 150000008052 alkyl sulfonates Chemical class 0.000 description 1
- 150000001408 amides Chemical group 0.000 description 1
- 150000001414 amino alcohols Chemical class 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-N ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 125000004104 aryloxy group Chemical group 0.000 description 1
- 125000004429 atoms Chemical group 0.000 description 1
- FLNKWZNWHZDGRT-UHFFFAOYSA-N azane;dihydrochloride Chemical compound [NH4+].[NH4+].[Cl-].[Cl-] FLNKWZNWHZDGRT-UHFFFAOYSA-N 0.000 description 1
- WPKYZIPODULRBM-UHFFFAOYSA-N azane;prop-2-enoic acid Chemical compound N.OC(=O)C=C WPKYZIPODULRBM-UHFFFAOYSA-N 0.000 description 1
- JJTDIRSCDLGMRU-UHFFFAOYSA-O azanium;prop-2-enamide Chemical compound [NH4+].NC(=O)C=C JJTDIRSCDLGMRU-UHFFFAOYSA-O 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
- CPELXLSAUQHCOX-UHFFFAOYSA-M bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 description 1
- 150000007942 carboxylates Chemical class 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 150000001783 ceramides Chemical class 0.000 description 1
- 229960000541 cetyl alcohol Drugs 0.000 description 1
- 238000007385 chemical modification Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- 238000004132 cross linking Methods 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- DKJLEUVQMKPSHB-UHFFFAOYSA-N dimethyl-[3-(octadecanoylamino)propyl]-(2-oxo-2-tetradecoxyethyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC(=O)OCCCCCCCCCCCCCC DKJLEUVQMKPSHB-UHFFFAOYSA-N 0.000 description 1
- IJOBQWAGGNHDEV-UHFFFAOYSA-L disodium;2-[1-[2-(carboxylatomethoxy)ethyl]-2-heptyl-4,5-dihydroimidazol-1-ium-1-yl]acetate;hydroxide Chemical compound [OH-].[Na+].[Na+].CCCCCCCC1=NCC[N+]1(CCOCC([O-])=O)CC([O-])=O IJOBQWAGGNHDEV-UHFFFAOYSA-L 0.000 description 1
- ZPRZNBBBOYYGJI-UHFFFAOYSA-L disodium;2-[1-[2-(carboxylatomethoxy)ethyl]-2-undecyl-4,5-dihydroimidazol-1-ium-1-yl]acetate;hydroxide Chemical compound [OH-].[Na+].[Na+].CCCCCCCCCCCC1=NCC[N+]1(CCOCC([O-])=O)CC([O-])=O ZPRZNBBBOYYGJI-UHFFFAOYSA-L 0.000 description 1
- GEGKMYLSPGGTQM-UHFFFAOYSA-L disodium;3-[2-(2-carboxylatoethoxy)ethyl-[2-(octanoylamino)ethyl]amino]propanoate Chemical compound [Na+].[Na+].CCCCCCCC(=O)NCCN(CCC([O-])=O)CCOCCC([O-])=O GEGKMYLSPGGTQM-UHFFFAOYSA-L 0.000 description 1
- UCYFZDNMZYZSPN-UHFFFAOYSA-N docosyl(trimethyl)azanium Chemical compound CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C UCYFZDNMZYZSPN-UHFFFAOYSA-N 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000019414 erythritol Nutrition 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 239000008103 glucose Substances 0.000 description 1
- 238000001033 granulometry Methods 0.000 description 1
- 229920000591 gum Polymers 0.000 description 1
- FIKFOOMAUXPBJM-UHFFFAOYSA-N hepta-2,5-dienediamide Chemical compound NC(=O)C=CCC=CC(N)=O FIKFOOMAUXPBJM-UHFFFAOYSA-N 0.000 description 1
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- 150000001261 hydroxy acids Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 239000003999 initiator Substances 0.000 description 1
- 229910052500 inorganic mineral Inorganic materials 0.000 description 1
- XMBWDFGMSWQBCA-UHFFFAOYSA-M iodide Chemical compound [I-] XMBWDFGMSWQBCA-UHFFFAOYSA-M 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 239000004922 lacquer Substances 0.000 description 1
- JVTAAEKCZFNVCJ-UHFFFAOYSA-M lactate Chemical compound CC(O)C([O-])=O JVTAAEKCZFNVCJ-UHFFFAOYSA-M 0.000 description 1
- 150000003893 lactate salts Chemical class 0.000 description 1
- 235000021388 linseed oil Nutrition 0.000 description 1
- 239000000944 linseed oil Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 239000011707 mineral Substances 0.000 description 1
- 235000010755 mineral Nutrition 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000001421 myristyl 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])[H] 0.000 description 1
- 230000003472 neutralizing Effects 0.000 description 1
- 150000002823 nitrates Chemical class 0.000 description 1
- 125000001400 nonyl 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])[H] 0.000 description 1
- 239000007764 o/w emulsion Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid group Chemical class C(CCCCCCC\C=C/CCCCCCCC)(=O)O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-M palmitate Chemical compound CCCCCCCCCCCCCCCC([O-])=O IPCSVZSSVZVIGE-UHFFFAOYSA-M 0.000 description 1
- IPCSVZSSVZVIGE-UHFFFAOYSA-N palmitic acid group Chemical class C(CCCCCCCCCCCCCCC)(=O)O IPCSVZSSVZVIGE-UHFFFAOYSA-N 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 235000020957 pantothenol Nutrition 0.000 description 1
- 239000011619 pantothenol Substances 0.000 description 1
- 239000012188 paraffin wax Substances 0.000 description 1
- 239000012071 phase Substances 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- NJRWNWYFPOFDFN-UHFFFAOYSA-L phosphonate(2-) Chemical compound [O-][P]([O-])=O NJRWNWYFPOFDFN-UHFFFAOYSA-L 0.000 description 1
- 229910052697 platinum Inorganic materials 0.000 description 1
- 229920002189 poly(glycerol 1-O-monomethacrylate) polymer Polymers 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 235000020004 porter Nutrition 0.000 description 1
- 229940072033 potash Drugs 0.000 description 1
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Substances [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 1
- 235000015320 potassium carbonate Nutrition 0.000 description 1
- KWYUFKZDYYNOTN-UHFFFAOYSA-M potassium hydroxide Chemical compound [OH-].[K+] KWYUFKZDYYNOTN-UHFFFAOYSA-M 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
- FSYKKLYZXJSNPZ-UHFFFAOYSA-N sarcosine zwitterion Chemical compound C[NH2+]CC([O-])=O FSYKKLYZXJSNPZ-UHFFFAOYSA-N 0.000 description 1
- 229940079776 sodium cocoyl isethionate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 239000003381 stabilizer 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
- 239000000126 substance Substances 0.000 description 1
- 239000005720 sucrose Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- 230000000475 sunscreen Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 150000003512 tertiary amines Chemical class 0.000 description 1
- IOUUIFSIQMVYKP-UHFFFAOYSA-N tetradecyl acetate Chemical compound CCCCCCCCCCCCCCOC(C)=O IOUUIFSIQMVYKP-UHFFFAOYSA-N 0.000 description 1
- MHXBHWLGRWOABW-UHFFFAOYSA-N tetradecyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCCCCCCCCCCCCC MHXBHWLGRWOABW-UHFFFAOYSA-N 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 235000015112 vegetable and seed oil Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamins Natural products 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- WQZGKKKJIJFFOK-VFUOTHLCSA-N β-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
Abstract
Cosmetic composition contains an emulsion(s) comprising a silicone copolymer(s) of viscosity 10<6>to 10<8>cP obtained by reacting a polysiloxane (I) and a silicone compound(s) with at least two groups that react with the terminal groups of (I) using a catalyst, at least one of them containing one or two ethylenically unsaturated aliphatic groups. Cosmetic composition comprises a cosmetically acceptable medium, a non-cellulosic thickener(s) and an emulsion(s) comprising a silicone copolymer(s) of viscosity 10<6>to 10<8>cP obtained by reacting a polysiloxane (A) of formula (I) and a silicone compound(s) (B) with at least two groups that react with the terminal groups of (I) using a catalyst, at least one of (A) and (B) containing one or two ethylenically unsaturated aliphatic groups:R1-Si(R2)2-(-O-Si(R2)2-)n-O-Si(R2)2-R1 (I) R1=H or ethylenically unsaturated group, particularly vinyl, allyl or hexenyl;R2=1-20C alkyl, 5-6C cycloalkyl, 7-20C aralkyl or OH optionally with ether, amino, carboxyl, hydroxyl, thiol, ester, sulfonate or sulfate groups;and n=number giving a viscosity of 1 to 10<6>mm<2>/s.
Description
COSMETIC COMPOSITIONS CONTAINING AN OOPOLIME-RO VINYL DIMETHICONE / DIMETHICONE IN AQUEOUS EMULSION AND A THICKENER AND ITS UTILIZATIONS.
The present invention relates to novel cosmetic compositions comprising a cosmetically acceptable medium at least one ethylenic copolymer dimethicone / dimethicone unsaturation with a viscosity between 106 and 100,106 cP in an aqueous emulsion and at least one non-cellulosic thickener. It is well known that hair that has been sensitized (ie damaged and / or fragile) to varying degrees under the action of atmospheric agents or under the action of mechanical or chemical treatments, such as colorations, discolorations and / or permanent, are often difficult to untangle and comb, 'and they lack softness. In the compositions for the washing or treatment of keratin materials such as hair, the use of conditioning agents, particularly silicones, has already been recommended to facilitate the disentangling of the hair.
REF: 124200 hair and to communicate softness and flexibility. However, the cosmetic advantages mentioned above are accompanied unfortunately also in dried hair, by certain cosmetic effects considered undesirable, namely caking hairstyle (lack of lightness of the hair), lack of smoothness (inhomogeneous hair from root to the tip), an unpleasant touch, loaded, a stiffness of the hair and an interfiber adhesion that affects the hairstyle, in particular in repeated uses. These drawbacks are accentuated in the case of fine hair, which lacks liveliness and volume. In summary, it happens that current cosmetic compositions containing silicones do not completely satisfy. The applicant has now discovered that the association of at least one particular silicone copolymer with a viscosity comprised between 106 and 100.106 cP in aqueous emulsion with non-cellulose thickeners, makes it possible to remedy these drawbacks. Thus, after considerable research conducted in this matter, it has now been discovered by the Applicant that by using the combination of at least one specific silicone copolymer viscosity between 106 and 100'6 cP aqueous emulsion thickeners noncellulosic a compositions in particular for the hair, it is possible to limit, even suppress, the problems generally related to the use of such compositions, namely in particular the caking (touch loaded in repeated applications), the lack of smoothing and softness of the hair, maintaining the other advantageous cosmetic properties that are inherent in compositions based on conditioning agents. This association provides cosmetic properties (smoothing, lightness, softness) without the phenomenon of fat contribution to the keratin fibers. On the other hand, the compositions of the invention applied to the skin, particularly in the form of a foaming bath or shower gel, provide an improvement in the softness of the skin. Thus, according to the present invention will now propose novel cosmetic compositions comprising, in a cosmetically acceptable medium, at least one aqueous emulsion of at least one silicone copolymer as defined below, wherein the copolymer indicated, a viscosity between 106 and 100,106 cP and at least one non-cellulosic thickener. Another object of the invention relates to the use of an aqueous emulsion of at least one silicone copolymer defined below, with viscosity between 100106 cP and 10d, or for the manufacture of a cosmetic composition comprising a non-cellulosic thickener. The different objects of the invention will be detailed below. The set of meanings and definitions of the compounds used in the present invention given below are valid for the set of objects of the invention. The silicone copolymer generally has a dynamic viscosity, measured at the temperature of about 25 ° C and in shear rate of 0.01 Hz for a voltage of 1500 Pa, comprised between 106 and 100,106 cP and preferably between 5,106 cP and 30,106 cP. All measurements of dynamic viscosities given in the present application have been made at a temperature of about 25 ° C, in a Carri-Med CSL2-500. The silicone copolymer present in the composition according to the invention is in the form of an aqueous emulsion. By aqueous emulsion, it is meant an oil-in-water emulsion in which the siliconed copolymer is dispersed in the form of particles or droplets in the aqueous phase forming the continuous phase of the emulsion. This emulsion can be stabilized by a usual emulsifier system. This silicone emulsion can have a size of droplets or silicone particles ranging from 10 nm to 50 μm, and preferably between 0.3 μm and 20 μm. The size of the particles is measured by laser granulometry. The emulsifier system comprises surfactants commonly used in silicone emulsions. These surfactants can be nonionic, cationic, anionic or amphoteric or their mixtures such as those described below. The emulsifier system represents from 0.5% to 10% by weight relative to the total weight of the emulsion. The silicone copolymer results from the addition reaction, in the presence of a catalyst of at least
a) a polysiloxane of formula (I)
wherein: R1 designates a group capable of acting by chain addition reaction such as for example a hydrogen atom, an aliphatic group with an ethylenic unsaturation particularly vinyl, allyl or hexenyl. The R 2 groups of the formula (I) may in particular represent alkyl, alkenyl, cycloalkyl, aryl, alkylaryl or hydroxyl groups and may further comprise functional groups such as ethers, amines, carboxyls, hydroxyls, thiols, esters, sulfonates, sulfates. The alkyl groups have, for example, from 1 to 20 carbon atoms; the cycloalkyl groups have, for example, 5 or 6 carbon atoms; aryl groups are particularly phenyl groups; the alkenyl groups have in particular from 2 to 10 carbon atoms; the alkylaryl groups may have from 7 to 20 carbon atoms. More particularly R2 denotes methyl. n is an integer such that the polysiloxane of formula (I) preferably has a kinematic viscosity comprised between 1 and 1,106 mm2 / s, in particular from 5 to 5000. - (b) and at least one silicone compound comprising at least one and at most two groups capable of reacting with the Ri groups of the polysiloxane (a), at least one of the Ri radicals of the compounds of type (a) or (b) contains an aliphatic group having an ethylenic unsaturation. The compounds of type (b) are another polysiloxane of type (a) in which the Ri groups of the polysiloxane (b) are capable of reacting with the Ri groups of the polysiloxane (a). Preferably, the silicone copolymers are obtained in particular by addition reaction, in the presence of a hydrosilylation catalyst (for example a platinum catalyst), of at least: - (a) an alpha, omega-divinylpolydimethylsiloxane, and - (b) an alpha, omega-dihydrogen polydimethylsiloxane.
The kinematic viscosity is measured, for example, at 25 ° C according to ASTM 445, Appendix C. The silicone copolymers according to the invention are essentially non-crosslinked. The synthesis of these silicone emulsions is described particularly in the application EP-A-874017. Such emulsions are sold in particular under the name DC2-1997 cationic emulsion by the company Dow Corning. This emulsion comprises a copolymer a, tu-divinyldimethicone, tp-dihydrogenodimethicone with a dynamic viscosity of about 15106 cP, a cationic type emulsifier such as cetyltrimethylammonium chloride, a stabilizer of the hydroxyethylcellulose type and water. The silicone copolymer is preferably used in an amount between 0.05 and 10% by weight relative to the total weight of the composition. More preferably, this amount is between 0.1 and 5% by weight relative to the total weight of the composition. The aqueous emulsion of the silicone polymer represents from 0.5 to 15% by weight of the total weight of the composition.
The non-cellulosic thickeners according to the invention may be of natural or synthetic origin. Mention may be made, as natural thickeners which are suitable for the invention, of xanthan gums, scleroglucan, gellan, rhamsan, alginates, maltodextrin, starch and its derivatives, karava gum, locust bean flour, guar gums It is also possible to use these compounds after chemical modification, such as, for example, hydroxypropylguards. The purely synthetic thickeners according to the invention are advantageously polymers or copolymers of acrylic and / or methacrylic acid, such as the copolymers of acrylic acid / ethyl acrylate and the carboxyvinyl polymers. Examples of such polymers or copolymers are particularly the "carbomer" (CTFA) sold by the company GOLDRICH under the name Carbopol (CARBOPOL 980, 981, 954, 2984, 5984) or SYNTHALEN or the polyglyceryl methacrylate marketed by the company GUARDI N under the name Lubragel or also the polyglyceryl acrylate marketed under the name Hispagel by the Sociedad HISPANO QUÍMICA. Polyethylene glycols (PEG) and their derivatives can also be used as a thickening agent. They can also be used advantageously, as a thickening agent, polyacrylamide thickeners. These may be chosen in particular from: the crosslinked 2-acrylamido-2-methylpropane sulfonic homopolymers, the optionally crosslinked ammonium acrylamide and acrylate copolymers, the acrylamide (or methacrylamide) and methacryloyloxyethyltrimethylammonium chloride copolymers, optionally crosslinked, - the copolymers of acrylamide and of acid
2-acrylamido-2-methyl-propanesulfonic, partially or totally neutralized, optionally cross-linked. As the acrylamide / ammonium acrylate crosslinked copolymers used according to the present invention, mention may be made more particularly of the acrylamide / ammonium acrylate copolymers (5/95 by weight) crosslinked by an olefinic polyunsaturation crosslinking agent, such as divinylbenzene , tetraalyloxyethane, methylene bis-acrylamide, diallyl ether, polyallyl polyglyceryl ethers or alcohol allyl ethers of the series of sugars, such as erythritol, penteritritol, arabitol, mannitol, sorbitol or glucose. Analogous copolymers are described and prepared in French patent FR-2,416,723 and US-2,798,053 and US-2,923,692. In particular, this type of crosslinked copolymer is used in the form of a water-in-oil emulsion consisting of approximately 30% by weight of said copolymer, 25% by weight of paraffin oil, 4% by weight of sorbitan stearate mixture and of a hydrophilic ethoxylated derivative and 41% by weight of water. An emulsion of this kind is marketed under the name "BOZEPOL C" by the HOECHST Company. The copolymers of acrylamide and 2-acryl-2-methypropropanesulfonic acid, used according to the present invention, are copolymers crosslinked by an olefinic polyunsaturation compound, such as those mentioned above, and partially or totally neutralized by a neutralizing agent. such as soda, potash, ammonia or an amine such as triethanolamine or monoacetanolamine.
They can be prepared by co-polymerizing the acrylamide and sodium 2-acrylamido-2-methylpropanesulfonate via the radical via initiator agents of the azobis-isobutyronitrile type and by precipitation in an alcohol such as tert-butylbutanol. Copolymers obtained by copolymerization of 70 to 55 mol% of acrylamide and 30 to 45 mol% of 2-acrylamido-2-methylpropanesulfonate sodium are more particularly used. The crosslinking agent is used at concentrations of 10"4 to 4.10-4 moles per mole of monomer mixture These particular copolymers are incorporated into the compositions of the invention, preferably in the form of water-in-oil emulsions containing from 35 to 40% by weight of this copolymer, from 15 to 25% by weight of a mixture of isoparaffinic hydrocarbons of C? 2-C? 3 / from 3 to 8% by weight of polyethylene glycol lauryl ether in 7 moles of ethylene oxide and water An emulsion of this kind is marketed under the name "SEPIGEL 305" by the SEPPIC Company The crosslinker of acrylamide and crosslinked methacryloyloxyethyltrimethylammonium chloride according to the invention, is more particularly a copolymer obtained by copolymerization of acrylamide and quaternized dimethylaminoethylmethacrylate by methyl chloride, followed by crosslinking by an olefinic unsaturation compound, in particular methylene-bisacrylamide. more particularly a cross-linked acrylamide / methacryloyloxyethyltrimethanolammonium chloride copolymer (approximately 50/50 by weight) in the form of a dispersion, containing 50% by weight of said copolymer in mineral oil. This dispersion is marketed under the name "SALCARE SC92" by the company ALLIED COLLOIDS. A crosslinked homopolymer of methacryloyloxyethyltrimethylammonium chloride may be used preferably in the form of a reverse dispersion. These dispersions are marketed in particular under the names "SALCARE SC95" and "SALCARE SC96" by the company ALLIED COLLOIDS. The non-crosslinked copolymers of methacrylamide and methacryloyloxyethyltrimethylammonium chloride are, for example, the products sold under the trade names ROHAGIT KF 400 and KF720 by the company ROHM & HAAS.
Preferably, the polymers of the cosmetic compositions according to the present invention advantageously have a solution or dispersion, at 1% active material in water, a viscosity measured by means of Rheomat RM 180 rheometer, at 25 ° C, greater than 0.1 ps, and more advantageously even higher than 0.2 cp, at a shear rate of 200 s "1. According to the invention, the thickener (s) can represent from 0.001% to 20% by weight, preferably from 0.01% to 10% by weight and more particularly from 0.1 to 3% by weight relative to the total weight of the product. The final composition The compositions of the invention further contain, advantageously at least one surfactant selected from the anionic, amphoteric, nonionic surfactants or their mixtures which is generally present in an amount comprised between 0.1% and 60% by weight approximately, preferably between 3% and 40% and also more preferably between 5% and 30%, relative to the total weight of the composition The surfactants which are suitable for the embodiment of the present invention are particularly s following: (i) anionic surfactant (s): Its nature does not, in the context of the present invention, have a truly critical character. Thus, by way of example of anionic surfactants which can be used alone or as a mixture, in the context of the present invention, mention may be made in particular (non-limiting list) of the salts (in particular alkali metal salts, particularly sodium salts, ammonium, salts of amines, salts of aminoalcohols or magnesium salts) of the following compounds: alkyl sulfates, alkyl ether sulfates, alkylamidoethersulfates, alkylaryl polyethersulfates, monoglycerides sulfates; the alkylsulfonates, alkyl phosphates, alkylamide sulfonates, alkylarylsulfonates, α-olefin sulfonates, paraffin sulfonates; alkylsulfosuccinates, alkylether sulfosuccinates, alkylamidesulfosuccinates; the alkylsulfosuccinamates; the alkylsulfoacetates; acyl sarcosinates; the acyl isethionates and the N-acyl taurates, the alkyl or acyl radical comprising all these various compounds preferably having from 8 to 24 carbon atoms, and the aryl radical preferably being a phenyl or benzyl group. Among the anionic surfactants which can also be used, mention may also be made of salts of fatty acids such as the salts of oleic, ricinoleic, palmitic, stearic acids, copra oil acids or hydrogenated copra oil; acyl lactylates whose acyl radical comprises from 8 to 20 carbon atoms. It is also possible to use poorly anionic surfactants, such as alkyl D galactoside uronic acids and their salts, as well as polyoxyalkylenated carboxylic acid (C6-C24) alkyl, polyoxyalkylenated carboxylic alkyl (C6-C2) aryl ether acids, alkyl acids (C6-C24) polyoxyalkylenated carboxylic amido ether and its salts, in particular those comprising from 2 to 50 ethylene oxide groups, and mixtures thereof. Among the anionic surfactants, it is preferred to use the salts of alkyl sulfates and alkyl ether sulphates and their mixtures according to the invention.
(ii) Nonionic Surfactant (s) The nonionic surfactants are, also, well known compounds per se (see particularly in this respect "Handbook of surfactants" by MR PORTER, Blackie & Son (Glasgow and London), 1991, pages 116-178) and its nature does not, within the framework of the present invention, be critical. Thus, alcohols, alkylsols, alkylphenols or polyethoxylated, polypropoxylated or polyglycerolated fatty acids with a fatty chain comprising, for example, from 8 to 18 carbon atoms can be chosen from among the (non-limiting list), the number of which can be varied. of groups of ethylene oxide or propylene oxide, in particular between 2 and 50, and the number of glycerol groups can vary from 2 to 30. Copolymers of ethylene oxide and propylene, ethylene oxide condensates and of propylene on fatty alcohols; the polyethoxylated fatty amides preferably having from 2 to 30 moles of ethylene oxide, the polyglycerolated fatty amides comprising on average from 1 to 5 glycerol groups and in particular from 1.5 to 4; polyethoxylated fatty amines preferably having 2 to 30 moles of ethylene oxide; the oxyethylenated sorbitan fatty acid esters having from 2 to 30 moles of ethylene oxide; the fatty acid esters of sucrose, the polyethylene glycol fatty acid esters, the alkyl polyglycosides, the N-alkyl glucamine derivatives, the amine oxides such as the alkyl (Cι-Cu) amines or the oxides of N- acylaminopropylmorpholine. It will be appreciated that the alkyl polyglycosides constitute nonionic surfactants which enter particularly well within the framework of the present invention.
(iii) Amphoteric surfactant (s) (&). The amphoteric surfactants, whose nature is not critical in the context of the present invention, can be particularly (non-limiting list) derivatives of aliphatic secondary or tertiary amines, in which the aliphatic radical is a straight or branched chain comprising 8 to 22 carbon atoms and containing at least one water-solubilizing anionic group (for example carboxylate, sulfonate, sulfate, phosphate or phosphonate); Mention may also be made of (C8-C20) alkyl betaines, sulfobetaines, (C8-C20) alkyloxy (Ci-Cß) betaines or (C8-C20) alkyl amidoalkyl (Ci-CG) sulfobetaines. Among the derivatives of amines, there may be mentioned the products marketed under the name MIRANOL, such as those described in US-2,528,378 and US-2,781,354 and of structures:
R2-C0NHCH2CH2-N (R3) (R4) (CH2COO) (2)
wherein: R2 denotes an alkyl radical derived from an acid R2-COOH present in the hydrolysed copra oil, a heptyl, nonyl or undecyl radical, R3 designates a betahydroxyethyl group and R4 a carboxymethyl group; Y
R5- C ONHCH2 CH2 -N (B) (C) 3)
wherein: B represents -CH2-CH2OX ', C represents - (CH2) ZY, with Z = l or 2, X' designates the group -CH2CH2-COOH or a hydrogen atom Y 'designates -COOH or the radical - CH2-CHOH-S03H R5 designates an alkyl radical of an acid R9 -COOH present in the copra oil or in the hydrolyzed linseed oil, an alkyl radical, in particular of C7, Cg, Cu or C? 3, an alkyl radical of Cu and its iso form, an unsaturated C17 radical. These compounds are classified in the CTFA dictionary, 5th edition, 1993, under the names Disodium Cocoamphodiacetate, Disodium Lauroamphodiacetate, Disodium Caprylamphodiacetate, Disodium Capryloamphodiacetate, Disodium
Cocoamphodipropionate, Disodiun
Lauroamphodipropionate, Disodium
Caprylamphodipro ionate, Disodium Capryloamphodipropionate, Lauroamphodipropionic acid, Cocoamphodipropionic acid. By way of example, mention may be made of the cocoamphodiacetate marketed under the trade name MIRANOL C2M concentrated by the company RHONE POULENC. In the compositions according to the invention, mixtures of surfactants and in particular mixtures of anionic surfactants and mixtures of anionic surfactants and of amphoteric or nonionic surfactants are preferably used. A particularly preferred mixture is a mixture consisting of at least one anionic surfactant and at least one amphoteric surfactant. Preferably, an anionic surfactant selected from sodium (C 1 -C 4) sulfates, triethanolamine or ammonium alkyl, sodium (C 2 -C 4) alkyl e-tersulfates, triethanolamine or of oxyethylenated ammonium in 2.2 moles of ethylene oxide, sodium cocoyl isethionate and sodium alpha-olefin (C 4 -C 6) sulfonate and mixtures thereof with: either an amphoteric surfactant such as the amine derivatives so-called disodiumcococamphodipropionate or sodiumcocoanopropionate marketed in particular by the company RHONE POULENC under the trade name "MIRANOL C2M CONC" in aqueous solution at 38% active matter or under the name MIRANOL C32; or an zwitterionic amphoteric surfactant such as alkylbetaines, in particular cocobetaine marketed under the name "DEHYTON AB 30" in aqueous solution at 32% MA by the company HENKEL. Even more preferably, the compositions according to the invention may also contain at least one cationic surfactant. The cationic surfactants can be chosen from:
A) the quaternary ammonium salts of the following general formula (IV):
wherein X is an anion selected from the group of halides (chloride, bromide or iodide) or alkyl (C2-C) sulfates more particularly methylisulfate, phosphates, alkyl-o-alkylaryl sulphonates, anions derived from organic acid such as acetate or lactate, and i) the radicals Ri to R3, which may be identical or different, represent an aliphatic radical, linear or branched, comprising from 1 to 4 carbon atoms, or an aromatic radical such as aryl or alkylaryl. The aliphatic radicals can comprise heteroatoms such as particularly oxygen, nitrogen, sulfur, halogens. The aliphatic radicals are, for example, chosen from the radicals alkyl, alkoxy, alkylamide, R 4 denotes an alkyl radical, linear or branched, comprising from 16 to 30 carbon atoms. Preferably the cationic surfactant is a salt (for example chloride) of behenyl trimethylammonium. ii) the radicals Ri and R2, which may be identical or different, represent an aliphatic radical, linear or branched, comprising from 1 to 4 carbon atoms, or an aromatic radical such as aryl or alkylaryl. The aliphatic radicals can comprise heteroatoms such as particularly oxygen, nitrogen, sulfur, halogens. The aliphatic radicals are, for example, chosen from the alkyl, alkoxy, alkylamide and hydroxyalkyl radicals, including approximately from 1 to 4 carbon atoms; R3 and R4, identical or different, denote an alkyl radical, linear or branched, including from 12 to 30 carbon atoms, said radical comprising at least one ester or amide function. R3 and R4 are particularly chosen from alkyl (C2-C22) amido (C2-C6) alkyl radicals; alkyl (C12-C22) acetate; Preferably the cationic surfactant is a salt (for example chloride) of ammonium stearamidopropyldimethyl (myristylacetate). B) - the quaternary ammonium salts of the imidazolinium, for example that of the following formula (V):
wherein R 5 represents an alkenyl or alkyl radical comprising from 8 to 30 carbon atoms for example derived from the fatty acids of tallow, R 6 represents a hydrogen atom, an alkyl radical of Ci-Cj O an alkenyl or alkyl radical which comprises from 8 to 30 carbon atoms, R7 represents an alkyl radical of C? -C4 Re represents a hydrogen atom, an alkyl radical of C? -C4 X is an anion selected from the group of halides, phosphates, acetates, lactates, alkyl sulfates, alkyl-o-alkylarylsulfonates. Preferably, R 5 and R 6 denote a mixture of alkenyl or alkyl radicals comprising from 12 to 21 carbon atoms, for example derived from the fatty acids of tallow, R 7 denotes methyl, R 7 denotes hydrogen. A product of this kind is, for example, Quaternium-27 (CTFA 1997) or Quaternium-83 (CTFA 1997) marketed under the names "REWOQUAT" W 75, W90, W75PG, W75HPG by the WITCO Company, C) - salts of diammonium quaternary of formula (VI):
wherein R9 designates an aliphatic radical comprising approximately 16 to 30 carbon atoms, Rio, Rn, R.2 / i3 and Rn, identical or different are chosen from hydrogen or an alkyl radical comprising from 1 to 4 atoms of carbon, and X is an anion selected from the group of halides, acetates, phosphates, nitrates and methylisulfates. Such quaternary ammonium salts particularly comprise propanosebo diammonium dichloride. D) - the quaternary ammonium salts containing at least one ester function of formula (VII) below:
wherein: - R 5 is selected from C 1 -C 6 alkyl radicals and C 1 -C 3 hydroxyalkyl or dihydroxyalkyl radicals; Ri6 is chosen from: O - the radical Ri9 ~ c ~ - the linear or branched, saturated or unsaturated C1-C22 hydrocarbon radicals R2o, - the hydrogen atom, - R is chosen from O - the radical R21 ~ 9. ~ - branched, saturated or unsaturated branched C? -C6 linear hydrocarbon radicals R22, - the hydrogen atom, - R1, R19 and R21, identical or different, are chosen from linear or branched hydrocarbon radicals of C7-C2? , saturated or unsaturated;
- n, p and r, identical or different, are integers that are worth 2 to 6; - and is an integer that is worth 1 to 10; - x and z, identical or different, are integers that are worth 0 to 10; - X is a simple or complex anion, organic or inorganic; with the proviso that the sum of x + y + z equals 1 to 15, that when x is 0 then Ri6 designates R2o and that when z is equal to 0 then Rie designates R22. More particularly used are the ammonium salts of formula (VII) in which: - R 15 denotes a methyl or ethyl radical, - x and y are equal to 1; - z is equal to 0 or 1; - n, p and r are equal to 2; - Ri6 is chosen from:
O - the radical Ri9 - C, -C22 radicals, methyl, ethyl or hydrocarbon radicals - the hydrogen atom; - Ri7, 19 and R21 identical or different, are chosen from hydrocarbon radicals of C7-C2 ?, linear or branched, saturated or unsaturated; - Ris is chosen from: O - the radical R2i i. -the hydrogen atom. Such compounds are for example marketed under the names DEHYQUART by the company HENKEL, STE-PANQUAT by the company
STEPAN, NOXAMIUM by the CECA Company, REWOQUAT WE 18 by the REWO-WITCO Company. Among the quaternary ammonium salts, preference is given to behenyltrimethylammonium chloride, or else stearamidopropyl dimethyl (myristyl acetate) ammonium chloride marketed under the name "CERAPHYL 70" by the company VAN DYK, Quaternium-27 or Quaternium-83 marketed by the WITCO Society. The cationic surfactant is generally present in concentrations ranging between 0.1 and 10% by weight relative to the total weight of the composition and preferably between 0.5 and 7% by weight and more preferably between 1 and 5% by weight. The composition of the invention can also contain at least one additive selected from among thickeners, perfumes, pearlizing agents, preservatives, sunscreen silicone or not, vitamins, provitamins, cationic, amphoteric, anionic or non-ionic polymers. ionics, proteins, protein hydrolysates, 18-methyleicosanóic acid, hydroxy acids, panthenol, volatile or nonvolatile silicones, cyclic or linear or crosslinked, modified or not, ceramides, pseudoceramides, vegetable oils, animals , minerals or synthesis and any other additive classically used in the cosmetic field that does not affect the properties of the compositions according to the invention. These additives are present in the composition according to the invention in proportions that can range from 0 to 20% by weight relative to the total weight of the composition. The precise amount of each additive is easily determined by the person skilled in the art according to its nature and function. The compositions according to the invention can be used more particularly for washing or treating keratin materials such as hair, skin, eyelashes, eyebrows, nails, lips, scalp and more particularly hair. The compositions according to the invention can be compositions after washing with shampoo to rinse or not. The compositions according to the invention can also be detergent compositions such as shampoos, shower gels, foaming baths and can also be make-up removers. In this embodiment of the invention, the compositions comprise a washing base, generally aqueous. The surfactant (s) forming the washing base can be indistinctly chosen, alone or as a mixture, from the anionic, amphoteric and nonionic surfactants as defined above. The quantity and quality of the washing base are sufficient to give the final composition a satisfactory foaming and / or detergent power. Thus, according to the invention, the washing base can represent from 4% to 50% by weight, preferably from 6% to 35% by weight, and even more preferably from 8% to 25% by weight, of the total weight of the final composition. The subject of the invention is also a method of treating keratin materials such as skin or hair, characterized in that it consists in applying a cosmetic composition, such as defined above, to the keratin materials, and optionally rinsing with water. . Thus, this method according to the invention allows the maintenance of the styling, the treatment, the care or the washing or the make-up of the skin, of the hair or of any other keratin material. The compositions of the invention can also be in the form of compositions for perming, straightening, coloring or decolorization, or else in the form of rinsing compositions, of applying before or after coloring, decolouration, perming or straightening or also between the two stages of a permanent or an aligned. The compositions according to the invention can also be presented in the form of aqueous or hydroalcoholic lotions for the care of the skin and / or of the hair. The cosmetic compositions according to the invention may be in the form of gel, milk, cream, emulsion, thick lotion or foam and used for the skin, nails, eyelashes, lips and more particularly the hair. The compositions can be packaged in various forms, particularly in vaporizers, sprays or in aerosol containers in order to ensure application of the composition in vaporized form or in the form of a foam. Such forms of conditioning are indicated, for example, when it is desired to obtain a spray, a lacquer or a foam for the treatment of the hair. In all that follows or the foregoing, the percentages expressed are by weight. The invention will now be illustrated more fully with the help of the following examples which should not be considered as limiting the described embodiments. In the examples, MA means active material. In the following examples, trade names have the following definitions:
EXAMPLE 1 A preparation was prepared after shampooing according to the invention with the following composition:
- Mixture of myristyl, palmitate and myristyl stearate, cetyl and stearyl 0.5 g
- beheni ltrimethylammonium chloride (GENAMIN KDMP from CLARIANT) 1.1 g MA - 67% cationic emulsion of polydimethylsiloxane copolymer MA with alpha-omega vinyl / polydimethylsiloxane groups with alpha-omega hydrogen groups (DC-1997 from DOW CORNING) 1.36 g MA - mixture of cetyl alcohol and stearyl alcohol (50/50 by weight) 3 g lauryldimethicone-polyol 91% MA (Q2-5200 from DOW CORNING) 0.23 g MA - xanthan gum 0.2 g
- perfume, preservatives cs
- Water esp 100 g
This composition was applied on washed and drained hair. It was left to rest for 2 minutes, then rinsed with water. The hair treated with this preparation after washing with shampoo is smooth, smooth and easily unraveled.
It is noted that in relation to this date, the best method known to the applicant, to implement said invention is that which is clear from the manufacture of the objects to which it refers. Having described the invention as above, the content of the following is claimed as property.
Claims (23)
1. Cosmetic composition, characterized in that it comprises, in a cosmetically acceptable medium, at least one non-cellulosic thickener and at least one aqueous emulsion comprising: at least one silicone copolymer with a viscosity comprised between 106 and 100.106 cP resulting from the reaction of addition, in the presence of a catalyst, of at least: - (a) a polysiloxane of formula (I): wherein: R1 designates a group capable of reacting by chain addition reaction such as for example a hydrogen atom, a monounsaturated ethylenic aliphatic group particularly vinyl, allyl or hexenyl, the R2 groups of the formula (I) represent alkyl groups , having 1 to 20 carbon atoms, cycloalkyl with 5 or 6 carbon atoms, aryl, alkylaryl with 7 to 20 carbon atoms or hydroxyl, and may further comprise functional groups such as ethers, amines, carboxyls, hydroxyls, thiols, esters, sulfonates, sulfates. n is an integer such that the polysiloxane of formula (I) preferably has a kinematic viscosity comprised between 1 and 1,106 mm2 / s. - (b) and of at least one silicone compound comprising at least one and at most two groups capable of reacting with the Ri groups of the polysiloxane (a), containing at least one of the compounds of type (a) or (b) an aliphatic group with an ethylenic unsaturation.
2. composition according to claim 1, characterized in that R2 designates methyl.
3. Composition according to one of claims 1 or 2, characterized in that the compound of type (b) is another polysiloxane of type (a) in which the Ri groups of the polysiloxane (b) are capable of reacting with the Ri groups of the polysiloxane (a).
4. Composition according to any one of claims 1 to 3, characterized in that the silicone copolymer is obtained by the addition reaction, in the presence of a hydrosilylation catalyst, of at least: (a) an alpha, omega-divinyl polydimethylsiloxane, and - (b) an alpha-omega-dihydrogen polydimethylsiloxane.
5. Composition according to one of claims 1 to 4, characterized in that said emulsion of the silicone copolymer has a size of droplets or of silicone particles ranging from 10 nm to 50 um and preferably from 0.3 um to 20 um .
6. Composition according to any one of claims 1 to 5, characterized in that the aqueous emulsion of the silicone copolymer represents from 0.5 to 15% by weight of the total weight of the composition,
7. Composition according to any one of claims 1 to 6, characterized in that the silicone copolymer is present at a concentration comprised between 0.05 and 10% by weight with respect to the total weight of the composition.
8. Composition according to any one of the preceding claims, characterized in that the thickening agent is of natural or synthetic origin.
9. Composition according to the preceding claim, characterized in that the thickener of natural origin is chosen among the gums of xanthan, scleroglucan, gelano, rhamsan, alginates, maltodextrin, starch and its derivatives, gum karaya, carob flour, guar gums.
10. Composition according to claim 8, characterized in that the thickening agent is chosen among the polymers or copolymers of acrylic and / or methacrylic acid.
11. Composition according to claim 8, characterized in that the thickening agent is a copolymer of acrylamide or acrylamide derivative.
12. Composition according to any one of claims 1 to 8, characterized in that the thickening polyacrylamide is chosen from: the crosslinked 2-acrylamido-2-methylpropanesulfonic homopolymers, the optionally crosslinked acrylamide and ammonium acrylate copolymers, - the copolymers of acrylamide (or methacrylamide) and of methacryloyloxyethyl trimethylammonium chloride, optionally crosslinked, and the copolymers of acrylamide and 2-acrylamido-2-methyl-propanesulfonic acid partially or totally neutralized, optionally crosslinked.
13. Composition according to any one of claims 1 to 8, characterized in that the thickening agent is chosen from polyethylene glycols and their derivatives.
14. Composition according to any one of the preceding claims, characterized in that the thickening agent is present in a concentration comprised between 0.001% and 20% by weight with respect to the total weight of the composition, preferably between 0.01% and 10% by weight 3% in weigh
15. Composition according to any one of the preceding claims, characterized in that said siliconed copolymer is present in a concentration comprised between 0.05% and 10% by weight relative to the total weight of the composition, preferably between 0.1% and 5% by weight.
16. Composition according to any one of the preceding claims, characterized in that it also comprises at least one surfactant chosen from anionic, nonionic, amphoteric surfactants and their mixtures.
17. Composition according to claim 16, characterized in that the agent or surfactants is present at a concentration comprised between 0.1 and 60% by weight, preferably between 3% and 40% by weight, and even more preferably between 5% and 30% by weight, based on the total weight of the composition.
18. Composition according to any one of the preceding claims, characterized in that it also comprises at least one cationic surfactant.
19. Composition according to the preceding claim, characterized in that the cationic surfactant is present in concentrations ranging between 0.1% and 10% by weight with respect to the total weight of the composition and preferably between 0.5% and 7%. % by weight and more preferably between 1 and 5% by weight
20. Composition according to any one of the preceding claims, characterized in that it is presented in the form of a shampoo, after shampooing, of composition for the pre-salt, the straightening, the coloring or the discoloration of the hair, clarifying composition to be applied between the two stages of a permente or of a spraying, of washing composition for the body.
21. Use of a composition as defined in any one of the preceding claims, for washing or for the care of keratin materials.
22. Process for the treatment of keratin materials, such as hair, characterized in that it consists of applying a cosmetic composition according to one of claims 1 to 20 on said materials, then optionally rinsing with water.
23. Use of an emulsion of at least one silicone copolymer as defined in one of claims 1 to 5, in, or for the manufacture of a cosmetic composition comprising a non-cellulosic thickener.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9913099 | 1999-10-20 |
Publications (1)
Publication Number | Publication Date |
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MXPA00010166A true MXPA00010166A (en) | 2002-07-25 |
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