LU84416A1 - SOFT CLEANING COMPOSITION - Google Patents
SOFT CLEANING COMPOSITION Download PDFInfo
- Publication number
- LU84416A1 LU84416A1 LU84416A LU84416A LU84416A1 LU 84416 A1 LU84416 A1 LU 84416A1 LU 84416 A LU84416 A LU 84416A LU 84416 A LU84416 A LU 84416A LU 84416 A1 LU84416 A1 LU 84416A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- composition
- chosen
- composition according
- nonionic
- cleaning
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 73
- 238000004140 cleaning Methods 0.000 title claims description 23
- 239000002736 nonionic surfactant Substances 0.000 claims description 21
- -1 glucoside alkyl ethers Chemical class 0.000 claims description 18
- 229920000642 polymer Polymers 0.000 claims description 17
- 239000000243 solution Substances 0.000 claims description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 8
- 235000014113 dietary fatty acids Nutrition 0.000 claims description 8
- 239000000194 fatty acid Substances 0.000 claims description 8
- 229930195729 fatty acid Natural products 0.000 claims description 8
- 150000003254 radicals Chemical class 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 6
- HOVAGTYPODGVJG-UVSYOFPXSA-N (3s,5r)-2-(hydroxymethyl)-6-methoxyoxane-3,4,5-triol Chemical compound COC1OC(CO)[C@@H](O)C(O)[C@H]1O HOVAGTYPODGVJG-UVSYOFPXSA-N 0.000 claims description 4
- NBVZMBLJRHUOJR-UHFFFAOYSA-N [amino-[4-[6-[4-[amino(azaniumylidene)methyl]phenoxy]hexoxy]phenyl]methylidene]azanium;2-hydroxyethanesulfonate Chemical compound OCCS(O)(=O)=O.OCCS(O)(=O)=O.C1=CC(C(=N)N)=CC=C1OCCCCCCOC1=CC=C(C(N)=N)C=C1 NBVZMBLJRHUOJR-UHFFFAOYSA-N 0.000 claims description 4
- 206010000496 acne Diseases 0.000 claims description 4
- 125000001931 aliphatic group Chemical group 0.000 claims description 4
- 229920013820 alkyl cellulose Polymers 0.000 claims description 4
- 239000004599 antimicrobial Substances 0.000 claims description 4
- 229930182478 glucoside Natural products 0.000 claims description 4
- 229960001915 hexamidine Drugs 0.000 claims description 4
- 150000003445 sucroses Chemical class 0.000 claims description 4
- 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 claims description 3
- 229920002472 Starch Polymers 0.000 claims description 3
- 239000011149 active material Substances 0.000 claims description 3
- 125000000217 alkyl group Chemical group 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 235000010980 cellulose Nutrition 0.000 claims description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000006071 cream Substances 0.000 claims description 3
- 239000000839 emulsion Substances 0.000 claims description 3
- 150000004665 fatty acids Chemical class 0.000 claims description 3
- 239000000499 gel Substances 0.000 claims description 3
- HOVAGTYPODGVJG-UHFFFAOYSA-N methyl beta-galactoside Natural products COC1OC(CO)C(O)C(O)C1O HOVAGTYPODGVJG-UHFFFAOYSA-N 0.000 claims description 3
- 235000013336 milk Nutrition 0.000 claims description 3
- 239000008267 milk Substances 0.000 claims description 3
- 210000004080 milk Anatomy 0.000 claims description 3
- 239000000600 sorbitol Substances 0.000 claims description 3
- 235000019698 starch Nutrition 0.000 claims description 3
- 239000005725 8-Hydroxyquinoline Substances 0.000 claims description 2
- 208000002874 Acne Vulgaris Diseases 0.000 claims description 2
- 240000008886 Ceratonia siliqua Species 0.000 claims description 2
- 235000013912 Ceratonia siliqua Nutrition 0.000 claims description 2
- GHXZTYHSJHQHIJ-UHFFFAOYSA-N Chlorhexidine Chemical compound C=1C=C(Cl)C=CC=1NC(N)=NC(N)=NCCCCCCN=C(N)N=C(N)NC1=CC=C(Cl)C=C1 GHXZTYHSJHQHIJ-UHFFFAOYSA-N 0.000 claims description 2
- 244000060011 Cocos nucifera Species 0.000 claims description 2
- 235000013162 Cocos nucifera Nutrition 0.000 claims description 2
- 201000004624 Dermatitis Diseases 0.000 claims description 2
- 229920001353 Dextrin Polymers 0.000 claims description 2
- 239000004375 Dextrin Substances 0.000 claims description 2
- 229920002907 Guar gum Polymers 0.000 claims description 2
- 229920000881 Modified starch Polymers 0.000 claims description 2
- 206010052428 Wound Diseases 0.000 claims description 2
- 208000027418 Wounds and injury Diseases 0.000 claims description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 2
- 208000010668 atopic eczema Diseases 0.000 claims description 2
- 229960000686 benzalkonium chloride Drugs 0.000 claims description 2
- 229960003260 chlorhexidine Drugs 0.000 claims description 2
- 235000019425 dextrin Nutrition 0.000 claims description 2
- 125000000118 dimethyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 2
- 235000019325 ethyl cellulose Nutrition 0.000 claims description 2
- 229920001249 ethyl cellulose Polymers 0.000 claims description 2
- 150000002338 glycosides Chemical group 0.000 claims description 2
- 239000000665 guar gum Substances 0.000 claims description 2
- 235000010417 guar gum Nutrition 0.000 claims description 2
- 229960002154 guar gum Drugs 0.000 claims description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 2
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 2
- 229920000609 methyl cellulose Polymers 0.000 claims description 2
- 235000010981 methylcellulose Nutrition 0.000 claims description 2
- 235000019426 modified starch Nutrition 0.000 claims description 2
- 229920001206 natural gum Polymers 0.000 claims description 2
- 239000001301 oxygen Substances 0.000 claims description 2
- 229910052760 oxygen Inorganic materials 0.000 claims description 2
- 229960003540 oxyquinoline Drugs 0.000 claims description 2
- RARSHUDCJQSEFJ-UHFFFAOYSA-N p-Hydroxypropiophenone Chemical compound CCC(=O)C1=CC=C(O)C=C1 RARSHUDCJQSEFJ-UHFFFAOYSA-N 0.000 claims description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 claims description 2
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 claims description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 claims description 2
- MCJGNVYPOGVAJF-UHFFFAOYSA-N quinolin-8-ol Chemical compound C1=CN=C2C(O)=CC=CC2=C1 MCJGNVYPOGVAJF-UHFFFAOYSA-N 0.000 claims description 2
- 150000003839 salts Chemical class 0.000 claims description 2
- ICUTUKXCWQYESQ-UHFFFAOYSA-N triclocarban Chemical compound C1=CC(Cl)=CC=C1NC(=O)NC1=CC=C(Cl)C(Cl)=C1 ICUTUKXCWQYESQ-UHFFFAOYSA-N 0.000 claims description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims 1
- 239000000443 aerosol Substances 0.000 claims 1
- 125000004429 atom Chemical group 0.000 claims 1
- XKXHCNPAFAXVRZ-UHFFFAOYSA-N benzylazanium;chloride Chemical compound [Cl-].[NH3+]CC1=CC=CC=C1 XKXHCNPAFAXVRZ-UHFFFAOYSA-N 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 1
- 229920013821 hydroxy alkyl cellulose Polymers 0.000 claims 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
- 101150009274 nhr-1 gene Proteins 0.000 claims 1
- 229910052717 sulfur Inorganic materials 0.000 claims 1
- 239000011593 sulfur Substances 0.000 claims 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 11
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 210000002374 sebum Anatomy 0.000 description 7
- 238000005406 washing Methods 0.000 description 7
- GPRLSGONYQIRFK-MNYXATJNSA-N triton Chemical compound [3H+] GPRLSGONYQIRFK-MNYXATJNSA-N 0.000 description 6
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 5
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 5
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 5
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- 230000002421 anti-septic effect Effects 0.000 description 4
- 210000004209 hair Anatomy 0.000 description 4
- 239000004141 Sodium laurylsulphate Substances 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 238000006243 chemical reaction Methods 0.000 description 3
- 239000003599 detergent Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- GQPLMRYTRLFLPF-UHFFFAOYSA-N Nitrous Oxide Chemical compound [O-][N+]#N GQPLMRYTRLFLPF-UHFFFAOYSA-N 0.000 description 2
- 241000282372 Panthera onca Species 0.000 description 2
- 229920001213 Polysorbate 20 Polymers 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- DKGAVHZHDRPRBM-UHFFFAOYSA-N Tert-Butanol Chemical compound CC(C)(C)O DKGAVHZHDRPRBM-UHFFFAOYSA-N 0.000 description 2
- 239000004480 active ingredient Substances 0.000 description 2
- 210000004027 cell Anatomy 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 2
- HVYWMOMLDIMFJA-DPAQBDIFSA-N cholesterol Chemical compound C1C=C2C[C@@H](O)CC[C@]2(C)[C@@H]2[C@@H]1[C@@H]1CC[C@H]([C@H](C)CCCC(C)C)[C@@]1(C)CC2 HVYWMOMLDIMFJA-DPAQBDIFSA-N 0.000 description 2
- 238000001035 drying Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 229910052757 nitrogen Inorganic materials 0.000 description 2
- 239000000256 polyoxyethylene sorbitan monolaurate Substances 0.000 description 2
- 235000010486 polyoxyethylene sorbitan monolaurate Nutrition 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000002360 preparation method Methods 0.000 description 2
- 239000003755 preservative agent Substances 0.000 description 2
- 239000002904 solvent Substances 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 210000002268 wool Anatomy 0.000 description 2
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical compound OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
- YYGNTYWPHWGJRM-UHFFFAOYSA-N (6E,10E,14E,18E)-2,6,10,15,19,23-hexamethyltetracosa-2,6,10,14,18,22-hexaene Chemical compound CC(C)=CCCC(C)=CCCC(C)=CCCC=C(C)CCC=C(C)CCC=C(C)C YYGNTYWPHWGJRM-UHFFFAOYSA-N 0.000 description 1
- WRIDQFICGBMAFQ-UHFFFAOYSA-N (E)-8-Octadecenoic acid Natural products CCCCCCCCCC=CCCCCCCC(O)=O WRIDQFICGBMAFQ-UHFFFAOYSA-N 0.000 description 1
- ARIWANIATODDMH-AWEZNQCLSA-N 1-lauroyl-sn-glycerol Chemical compound CCCCCCCCCCCC(=O)OC[C@@H](O)CO ARIWANIATODDMH-AWEZNQCLSA-N 0.000 description 1
- LQJBNNIYVWPHFW-UHFFFAOYSA-N 20:1omega9c fatty acid Natural products CCCCCCCCCCC=CCCCCCCCC(O)=O LQJBNNIYVWPHFW-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- 241000416162 Astragalus gummifer Species 0.000 description 1
- UXVMQQNJUSDDNG-UHFFFAOYSA-L Calcium chloride Chemical compound [Cl-].[Cl-].[Ca+2] UXVMQQNJUSDDNG-UHFFFAOYSA-L 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- 206010018910 Haemolysis Diseases 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- ARIWANIATODDMH-UHFFFAOYSA-N Lauric acid monoglyceride Natural products CCCCCCCCCCCC(=O)OCC(O)CO ARIWANIATODDMH-UHFFFAOYSA-N 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- 229920013806 TRITON CG-110 Polymers 0.000 description 1
- BHEOSNUKNHRBNM-UHFFFAOYSA-N Tetramethylsqualene Natural products CC(=C)C(C)CCC(=C)C(C)CCC(C)=CCCC=C(C)CCC(C)C(=C)CCC(C)C(C)=C BHEOSNUKNHRBNM-UHFFFAOYSA-N 0.000 description 1
- 229920001615 Tragacanth Polymers 0.000 description 1
- XEFQLINVKFYRCS-UHFFFAOYSA-N Triclosan Chemical compound OC1=CC(Cl)=CC=C1OC1=CC=C(Cl)C=C1Cl XEFQLINVKFYRCS-UHFFFAOYSA-N 0.000 description 1
- BAECOWNUKCLBPZ-HIUWNOOHSA-N Triolein Natural products O([C@H](OCC(=O)CCCCCCC/C=C\CCCCCCCC)COC(=O)CCCCCCC/C=C\CCCCCCCC)C(=O)CCCCCCC/C=C\CCCCCCCC BAECOWNUKCLBPZ-HIUWNOOHSA-N 0.000 description 1
- PHYFQTYBJUILEZ-UHFFFAOYSA-N Trioleoylglycerol Natural products CCCCCCCCC=CCCCCCCCC(=O)OCC(OC(=O)CCCCCCCC=CCCCCCCCC)COC(=O)CCCCCCCC=CCCCCCCCC PHYFQTYBJUILEZ-UHFFFAOYSA-N 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- 239000008346 aqueous phase Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 210000004369 blood Anatomy 0.000 description 1
- 239000008280 blood Substances 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 239000001110 calcium chloride Substances 0.000 description 1
- 229910001628 calcium chloride Inorganic materials 0.000 description 1
- 235000012000 cholesterol Nutrition 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- 230000009089 cytolysis Effects 0.000 description 1
- 239000002274 desiccant Substances 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- SZXQTJUDPRGNJN-UHFFFAOYSA-N dipropylene glycol Chemical class OCCCOCCCO SZXQTJUDPRGNJN-UHFFFAOYSA-N 0.000 description 1
- 238000004090 dissolution Methods 0.000 description 1
- PRAKJMSDJKAYCZ-UHFFFAOYSA-N dodecahydrosqualene Natural products CC(C)CCCC(C)CCCC(C)CCCCC(C)CCCC(C)CCCC(C)C PRAKJMSDJKAYCZ-UHFFFAOYSA-N 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 210000003743 erythrocyte Anatomy 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000004744 fabric Substances 0.000 description 1
- 238000001914 filtration Methods 0.000 description 1
- 230000008588 hemolysis Effects 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 239000001272 nitrous oxide Substances 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000002504 physiological saline solution Substances 0.000 description 1
- 229920002401 polyacrylamide Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 238000003825 pressing Methods 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 239000012429 reaction media Substances 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 229930195734 saturated hydrocarbon Natural products 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 229940031439 squalene Drugs 0.000 description 1
- TUHBEKDERLKLEC-UHFFFAOYSA-N squalene Natural products CC(=CCCC(=CCCC(=CCCC=C(/C)CCC=C(/C)CC=C(C)C)C)C)C TUHBEKDERLKLEC-UHFFFAOYSA-N 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 125000004434 sulfur atom Chemical group 0.000 description 1
- 230000000475 sunscreen effect Effects 0.000 description 1
- 239000000516 sunscreening agent Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 235000010487 tragacanth Nutrition 0.000 description 1
- 239000000196 tragacanth Substances 0.000 description 1
- 229940116362 tragacanth Drugs 0.000 description 1
- PHYFQTYBJUILEZ-IUPFWZBJSA-N triolein Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OCC(OC(=O)CCCCCCC\C=C/CCCCCCCC)COC(=O)CCCCCCC\C=C/CCCCCCCC PHYFQTYBJUILEZ-IUPFWZBJSA-N 0.000 description 1
- 229940117972 triolein Drugs 0.000 description 1
- 230000000007 visual effect Effects 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
-
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/416—Quaternary ammonium compounds
-
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/43—Guanidines
-
- 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
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/60—Sugars; Derivatives thereof
- A61K8/604—Alkylpolyglycosides; Derivatives thereof, e.g. esters
-
- 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
- A61K8/73—Polysaccharides
- A61K8/731—Cellulose; Quaternized cellulose derivatives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- A61K8/817—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a single or double bond to nitrogen or by a heterocyclic ring containing nitrogen; Compositions or derivatives of such polymers, e.g. vinylimidazol, vinylcaprolactame, allylamines (Polyquaternium 6)
- A61K8/8176—Homopolymers of N-vinyl-pyrrolidones. Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/84—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
- A61K8/88—Polyamides
-
- 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
- A61Q5/02—Preparations for cleaning the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Dermatology (AREA)
- Cosmetics (AREA)
- Detergent Compositions (AREA)
Description
Composition de nettoyage doux.Gentle cleaning composition.
La présente invention est relative à de nouvelles compositions de nettoyage doux utilisables notamment pour le nettoyage des cheveux et de la peau.The present invention relates to new gentle cleaning compositions which can be used in particular for cleaning the hair and the skin.
Les tensio-actifs non ionigues sont bien connus dans l’état de la technique et ont été utilisés couramment dans les préparations de nettoyage de la peau ou des cheveux.Non-ionic surfactants are well known in the art and have been commonly used in preparations for cleaning the skin or hair.
La demanderesse a découvert, qu'en associant certains des agents tensio-actifs non ioniques avec des polymères non-ioniques bien particuliers, il était possible d’obtenir une composition de nettoyage doux, présentant des propriétés d'innocuité et de détergence améliorées par rapport aux composition ne contenant que le tensio-actif non-ionique.The Applicant has discovered that by combining certain of the nonionic surfactants with very specific nonionic polymers, it was possible to obtain a mild cleaning composition, having improved safety and detergency properties compared to to compositions containing only the nonionic surfactant.
La demanderesse a en effet découvert qu'en associant certains tensio-actifs non-ioniques avec certains polymères non-ioniques, on obtenait une composition très peu agressive dont les points de demi-lyse des hématies sont relativement élevés par rapport aux compositions dites de nettoyage doux à base de tensio-actifs non-ioniques.The Applicant has in fact discovered that by combining certain nonionic surfactants with certain nonionic polymers, a very mild composition is obtained, the red cell half-lysis points of which are relatively high compared to the so-called cleaning compositions. mild based on non-ionic surfactants.
La demanderesse a découvert également que l'on améliorait de façon importante la détergence de la composition par rapport aux propriétés de détergence du tensio-actif non-ionique utilisé seul dans une composition classique.The Applicant has also discovered that the detergency of the composition is significantly improved compared to the detergency properties of the nonionic surfactant used alone in a conventional composition.
Afin de déterminer la détergence et l'agressivité des compositions de nettoyage la demanderesse a mis au point les deux essais suivants.In order to determine the detergency and the aggressiveness of the cleaning compositions, the applicant has developed the following two tests.
Mesure de l'agressivité L'agressivité est déterminée par hémolyse des hématies d'échantillon de sang. On examine à cet effet les points de demi-lyse des différentes compositions. On appelle point de demi-lyse la concentration du produit dilué dans du sérum physiologique qui provoque la lyse de 501 des hématies. iMeasuring aggressiveness Aggressiveness is determined by hemolysis of red blood cells from a blood sample. To this end, the half-lysis points of the different compositions are examined. The half-lysis point is the concentration of the product diluted in physiological saline which causes the lysis of 501 red cells. i
Plus le point de demi-lyse est élevé, moins la composi-?./ tion de nettoyage est agressive.The higher the half-lysis point, the less aggressive the cleaning composition.
22
Determination de la détergenceDetergency determination
On dépose sur des échantillons de laine une quantité déterminée de sébum sous la forme d'une tache. Après lavage des échantillons dans des conditions standards avec une machine automatique et séchage, la quantité de sébum résiduelle est mise en évidence par révélation à l'aide d'acide osmique. On obtient ainsi une tache qui, suivant la quantité de sébum restant, a une coloration allant du gris pâle au noir. Plus la tache est foncée, plus la quantité de sébum restant est importante et plus la détergence de la composition étudiée est faible.A determined quantity of sebum is deposited on wool samples in the form of a stain. After washing the samples under standard conditions with an automatic machine and drying, the amount of residual sebum is revealed by revelation using osmic acid. A spot is thus obtained which, depending on the amount of sebum remaining, has a color ranging from pale gray to black. The darker the stain, the greater the amount of sebum remaining and the lower the detergency of the composition studied.
La méthode suivante est utilisée et on effectue toutes les mesures en double. Sur un échantillon de laine vierge on applique 70 mg de sébum artificiel ayant la composition suivante : k Squalène 97% 19-dThe following method is used and all measurements are performed in duplicate. 70 mg of artificial sebum having the following composition are applied to a sample of virgin wool: k Squalene 97% 19-d
Cholestérol puriss. 5%Cholesterol puriss. 5%
Trioléïne technique 45%Technical triolein 45%
Acide oléîque pur 31%.Pure oleic acid 31%.
On procède ensuite au lavage avec une machine automatique principalement constituée d'un plateau mobile, d'un rouleau presseur et de gicleurs délivrant l'eau pour le rinçage.Washing is then carried out with an automatic machine mainly consisting of a movable plate, a pressing roller and nozzles delivering the water for rinsing.
Le plateau, lorsqu'il se trouve en action, est animé d'un mouvement alternatif et d'une fréquence de 20 passages par minute (+ ou - 3 secondes).The plate, when in action, is driven by an alternating movement and a frequency of 20 passages per minute (+ or - 3 seconds).
Après avoir fixé l'échantillon sur le plateau, on dépose sur le tissu, 0,75 ml de la composition à tester et on^effec-tue 60 passages de rouleau (3 minutes). On rince ensuite en dispersant 240 ml d'eau et en déplaçant plateau et rouleau pendant 3 minutes (60 passages).After fixing the sample on the plate, 0.75 ml of the composition to be tested is placed on the fabric and 60 roll passes are made (3 minutes). Then rinse by dispersing 240 ml of water and moving the tray and roller for 3 minutes (60 passes).
Le lavage est ensuite répété avec 0,5 ml de composition a tester, 60 passages de rouleau et rinçage avec 240 ml d’eau et 120 passages du rouleau (6 minutes).The washing is then repeated with 0.5 ml of composition to be tested, 60 passages of roller and rinsing with 240 ml of water and 120 passages of the roller (6 minutes).
On révèle le sébum résiduel à l'aide de vapeurs d'acide osmique. Dans une boîte étanche, on libère de l'acide osmique que l'on laisse en contact avec l'échantillon pendant 5 minutes, ce laps de temps est suffisant pour que la réaction avec le'/ sébum soit complète. / JThe residual sebum is revealed using osmic acid vapors. In a sealed box, osmic acid is released which is left in contact with the sample for 5 minutes, this period of time is sufficient for the reaction with the sebum to be complete. / J
33
La mesure de l'intensité de la couleur de la tache est effectuée par une méthode visuelle en prenant comme témoin une solution de laurylsulfate de sodium à une teneur de laurylsul-fate de sodium de X%. On compare l'intensité de la tache de la composition à tester à l'intensité la plus proche de la solu--. tion de laurylsulfate de sodium. On utilise à cette fin des solution témoins à des concentrations variables de laurylsulfate de sodium.The intensity of the color of the stain is measured by a visual method using as a control a solution of sodium lauryl sulphate at a sodium lauryl sulphate content of X%. The intensity of the stain of the composition to be tested is compared to the intensity closest to the solution. tion of sodium lauryl sulfate. Control solutions are used for this purpose at varying concentrations of sodium lauryl sulfate.
L'activité détergente est exprimée en équivalent de laurylsulfate de sodium.The detergent activity is expressed in equivalent of sodium lauryl sulfate.
Un objet de l'invention est donc constitué par une composition de nettoyage contenant au moins certains tensio-actifs non ioniques associés avec certains polymères non ioniques.An object of the invention therefore consists of a cleaning composition containing at least certain nonionic surfactants associated with certain nonionic polymers.
Un autre objet de l'invention est constitué par un procédé de nettoyage mettant en oeuvre la composition précitée.Another object of the invention consists of a cleaning process using the above composition.
D'autres objets apparaîtront à la lecture de la description et des exemples qui suivent.Other objects will appear on reading the description and the examples which follow.
La composition de nettoyage doux conforme à l'invention est essentiellement caractérisée par le fait qu'elle contient dans un milieu cosmétiquement acceptable au moins un tensio-actif non-ionique (I) choisi parmi : (i) les alkyléthers de glucoside répondant à la formule : ch2oh r ch2oh η A--0 y-0 \L_y--νλρ—R .«> OH OH L 'OH - n dans laquelle R désigne un radical alkyle ayant 8 ä 10 atomes de carbone, n est égal à 0, 1, 2, 3 ou 4; (ii) les méthyl glucosides oxyethylénés ou oxypropylénés; (iii) le sesquistëarate de méthyl glucoside éventuellement oxyéthylêné; (iv) le dioléate de méthyl glucoside oxyéthylêné; (v) les esters de sucrose ou les esters de saccharose; / (vi) les -o<.-diols polyglycérolés répondant à la formule /j R-jCHOH - CH2-0fCH2-CH0H-CE2-0.?nH j /The mild cleaning composition in accordance with the invention is essentially characterized in that it contains, in a cosmetically acceptable medium, at least one nonionic surfactant (I) chosen from: (i) the glucoside alkyl ethers corresponding to the formula: ch2oh r ch2oh η A - 0 y-0 \ L_y - νλρ — R. «> OH OH OH - n in which R denotes an alkyl radical having 8 to 10 carbon atoms, n is equal to 0 , 1, 2, 3 or 4; (ii) oxyethylenated or oxypropylenated methyl glucosides; (iii) optionally oxyethylated methyl glucoside sesquistearate; (iv) oxyethylenated methyl glucoside dioleate; (v) sucrose esters or sucrose esters; / (vi) the -o <.- polyglycerolated diols corresponding to the formula / j R-jCHOH - CH2-0fCH2-CH0H-CE2-0.?nH j /
Ui· 4 dans laquelle R^ désigne un radical ou un mélange de radicaux aliphatiques, cycloaliphatiques ou arylaliphatiques, les chaînes aliphatiques pouvant comporter des atomes d'oxygène ou de soufre, n est un nombre quelconque supérieur à 1 et égal ou inférieur à 10, ces composés sont décrits plus particulièrement dans le brevet français 2.091.516; (vii) les hydroxyalcoyl polyglycosides comportant un radical alcoyle ayant de 11 à 18 atomes de carbone et un nombre de motifs glycosides compris entre 3 et 25, ces composés sont décrits plus particulièrement dans la demande de brevet français 2.397.185, et au moins un polymère non ionique choisi parmi : (i) les alkylcelluloses; (ii) les polyhydroxyalkylcelluloses; (iii) les poly- /à-alanines ; (iv) des dérivés non-ioniques d'amidon tels gue les hydroxy-propyléthers d'amidon ou des dérivés hydroxypropylés de gomme de Guar tels que par exemple les produits vendus sous les dénominations JAGUAR HP 60 et JAGUAR HP 8 par la Société MEYHALL; (v) des gommes naturelles telles que les gommes adragante, arabique, de caroube; (vi) la polyvinylpyrrolidone; (vii) des polyholosides tels que les celluloses, les amidons, les dextrines.Ui · 4 in which R ^ denotes a radical or a mixture of aliphatic, cycloaliphatic or arylaliphatic radicals, the aliphatic chains possibly comprising oxygen or sulfur atoms, n is any number greater than 1 and equal to or less than 10, these compounds are described more particularly in French patent 2,091,516; (vii) hydroxyalkyl polyglycosides comprising an alkyl radical having from 11 to 18 carbon atoms and a number of glycoside units between 3 and 25, these compounds are described more particularly in French patent application 2,397,185, and at least one nonionic polymer chosen from: (i) alkylcelluloses; (ii) polyhydroxyalkylcelluloses; (iii) poly- / to-alanines; (iv) nonionic starch derivatives such as starch hydroxypropyl ethers or hydroxypropylated guar gum derivatives such as for example the products sold under the names JAGUAR HP 60 and JAGUAR HP 8 by the company MEYHALL; (v) natural gums such as tragacanth, arabic, carob gums; (vi) polyvinylpyrrolidone; (vii) polyholosides such as celluloses, starches, dextrins.
L'agent tensio-actif non ionique tel que défini ci-dessus est de préférence utilisé dans les proportions de 5 à 15% en poids exprimé en matière active par rapport au poids total de la composition.The nonionic surfactant as defined above is preferably used in the proportions of 5 to 15% by weight expressed as active material relative to the total weight of the composition.
Les polymères non ioniques sont utilisés de préférence dans les proportions comprises entre 0,1 et 10% en poids exprimés en matière active par rapport au poids total de la composition.The nonionic polymers are preferably used in the proportions of between 0.1 and 10% by weight expressed as active material relative to the total weight of the composition.
Les alkylcelluloses sont choisies plus particulièrement parmi les méthyl- et éthylcelluloses et les polyhydroxyalkyl- ^ celluloses sont choisies plus particulièrement parmi les /The alkylcelluloses are chosen more particularly from methyl- and ethylcelluloses and the polyhydroxyalkyl- celluloses are chosen more particularly from /
polyhydroxyéthyl-, hydroxypropylméthyl-, ou hydroxypropylce^tVpolyhydroxyethyl-, hydroxypropylmethyl-, or hydroxypropylce ^ tV
5 luloses ayant un poids moléculaire compris entre 60.000 et 1.000.000.5 luloses with a molecular weight between 60,000 and 1,000,000.
Les poly-/t>-alanines sont plus particulièrement décrites dans la demande de brevet belge n° 208.516 déposée par la demanderesse.The poly- / t> -alanines are more particularly described in Belgian patent application No. 208.516 filed by the applicant.
'. Ces polymères comportent de 50 à 100¾ de motifs répéti tifs de formule ; JL CH _ CH _ CO_N J— (I)'. These polymers comprise from 50 to 100% of repeating units of formula; JL CH _ CH _ CO_N J— (I)
I I II I I
R3 R2 R1 et de 0 à 50% de motifs répétitifs du type polyacrylamide correspondant à la formule suivante : r- R9 1 2 -j —CH - C--(II) I )R3 R2 R1 and from 0 to 50% of repeating units of the polyacrylamide type corresponding to the following formula: r- R9 1 2 -j —CH - C - (II) I)
Liu c = o JLiu c = o J
Ahr^^ dans lesquelles représente un atome d'hydrogène, ou un radical pris dans le groupe constitué par les radicaux suivants : (i) - CH2 -Ahr ^^ in which represents a hydrogen atom, or a radical taken from the group consisting of the following radicals: (i) - CH2 -
(ii) - CH20H(ii) - CH20H
(iii) - (CH2) , - CHg n' étant 0 ou un nombre entier de 1 à 11 r' (iv) - CH - ΙΓ \ r" r1 et r", identiques ou différents, représentant un atome d'hydrogène ou un radical alkyle de 1 à 3 atomes de carbone? et (v) - (CH2-CH2-0)-^-H m étant compris entre 1 et 10, et, R2 et R^ représentent un atome d'hydrogène ou un radical méthyle.(iii) - (CH2), - CHg n 'being 0 or an integer from 1 to 11 r' (iv) - CH - ΙΓ \ r "r1 and r", identical or different, representing a hydrogen atom or an alkyl radical of 1 to 3 carbon atoms? and (v) - (CH2-CH2-0) - ^ - H m being between 1 and 10, and, R2 and R ^ represent a hydrogen atom or a methyl radical.
Ces polymères sont préparés plus particulièrement par polymérisation de 1'acrylamide, comme décrit dans le brevet américain 4.082.730. Ces polymères ont de préférence un poids j moléculaire compris entre 500 et 100.000 et plus particulierery ment entre 2000 et 60.000. /// 6These polymers are more particularly prepared by polymerization of acrylamide, as described in US Patent 4,082,730. These polymers preferably have a molecular weight between 500 and 100,000 and more particularly between 2000 and 60,000. /// 6
Les compositions conformes à l'invention peuvent contenir ce qui constitue un autre objet de l'invention d'autres agents tensio-actifs non ioniques (II) différents des agents tensio-actifs non ioniques (I) mentionnés ci-dessus. Ces agents tensio-actifs non-ioniques (II) sont choisis parmi les esters d'acide gras du sorbitol polyoxyéthylénés tel que le monolau-rate de sorbitan polyoxyéthyléné à 20 moles d'oxyde d'éthylène ou encore les esters partiels d'acide gras et de glycérol oxyéthylénés comme le monolaurate de glycérol polyoxyéthyléné.The compositions in accordance with the invention may contain what constitutes another object of the invention of other nonionic surfactants (II) different from the nonionic surfactants (I) mentioned above. These nonionic surfactants (II) are chosen from polyoxyethylenated sorbitol fatty acid esters such as polyoxyethylenated sorbitan monolau-spleen with 20 moles of ethylene oxide or also partial fatty acid esters and oxyethylenated glycerol such as polyoxyethylenated glycerol monolaurate.
Ces agents tensio-actifs (II) sont connus en eux-mêmes pour être peu agressifs et conduisent encore à l'amélioration des propriétés de la composition de nettoyage conforme à 1'invention.These surfactants (II) are known in themselves to be not very aggressive and further lead to the improvement of the properties of the cleaning composition according to the invention.
Une forme de réalisation préférée de l'invention est constituée par une composition de nettoyage contenant en particulier l'un des différents agents tensio-actifs non-ioniques (i) , (ii), (iii) , (iv) , (vi) , (vii) mentionnés ci-dessus associés avec les polymères non ioniques des groupes (i) à (vii) .A preferred embodiment of the invention consists of a cleaning composition containing in particular one of the various non-ionic surfactants (i), (ii), (iii), (iv), (vi) , (vii) mentioned above associated with the nonionic polymers of groups (i) to (vii).
Une autre forme de réalisation préférée est constituée par des compositions contenant les agents tensio-actifs non-ioniques définis dans les paragraphes (i) à (vii) associés avec des polymères non ioniques tels que définis ci-dessus et au moins un agent tensio-actif non ionique (II) choisi parmi les esters d'acide gras du sorbitol polyoxyéthyléné et les esters partiels d'acide gras et de glycérol oxyéthylénés définis ci-dessus.Another preferred embodiment consists of compositions containing the nonionic surfactants defined in paragraphs (i) to (vii) combined with nonionic polymers as defined above and at least one surfactant. non-ionic active (II) chosen from fatty acid esters of polyoxyethylenated sorbitol and partial esters of fatty acid and glycerol oxyethylenated defined above.
La demanderesse a découvert en particulier qu'avec les compositions conformes à l'invention, contenant le tensio-actif non ionique (I) (i) , (ii) , (iii) 7 (iv) , (vi) et (vii) susdé- finis avec l'un des polymères non ioniques egalement définis ci-dessus dans les proportions indiquées, on obtenait une meilleure innocuité tout en augmentant la détergence. Ainsi, une composition contenant 10% d'alkyléther de glucoside vendu sous la dénomination TRITON CG-110-60 a une activité détergente équivalente à 1,25% de laurylsulfate de sodium et un point de ^ demi-lyse de 1% alors qu'une composition contenant 8% du mêim/"/The Applicant has discovered in particular that, with the compositions in accordance with the invention, containing the nonionic surfactant (I) (i), (ii), (iii) 7 (iv), (vi) and (vii) above defined with one of the nonionic polymers also defined above in the proportions indicated, better safety was obtained while increasing the detergency. Thus, a composition containing 10% of glucoside alkyl ether sold under the name Triton CG-110-60 has a detergent activity equivalent to 1.25% of sodium lauryl sulfate and a point of half-lysis of 1% while a composition containing 8% of the same / "/
UU
7 agent tensio-actif non ionique TRITON CG-110 avec l'hydroxy-éthylcellulose (0,3%) a un pouvoir détergent équivalent à celui d'une solution à 3% de laurylsulfate de sodium et un point de demi-lyse de 1,23%.7 non-ionic surfactant TRITON CG-110 with hydroxyethylcellulose (0.3%) has a detergent power equivalent to that of a 3% solution of sodium lauryl sulfate and a half-lysis point of 1 , 23%.
Les compositions de nettoyage conformes à l'invention *. sont utilisables pour le nettoyage de la peau et des cheveux.The cleaning compositions according to the invention *. can be used for cleaning the skin and hair.
Une application particuliérement préférée est leur utilisation pour le nettoyage des peaux à problème telles que acnéiques ou à points noirs.A particularly preferred application is their use for cleaning problem skin such as acne or blackheads.
Selon une forme de réalisation on peut adjoindre un antiseptique de façon à obtenir un produit traitant utilisable dans le domaine dermatologique pour le nettoyage des plaies, l'hygiêne féminine intime, le traitement de l'ezcéma et nettement moins agressif que les produits de ce type existant déjà sur le marché.According to one embodiment, an antiseptic can be added so as to obtain a treating product which can be used in the dermatological field for cleaning wounds, intimate female hygiene, the treatment of eczema and clearly less aggressive than products of this type. already existing on the market.
Les agents antiseptiques utilisables dans cette forme de réalisation de l'invention sont des agents connus en eux-mêmes et couramment utilisés dans les compositions antiseptiques. On peut citer à cet effet, le diisëthionate d'hexamidine, le 2,4,4'-trichloro-2'-hydroxy-biphényléther, la chlorhexidine, le digluconate de chlorhexidine, le chlorure de 4-benzalkonium, le 3,4,4'-trichlorocarbanilide, la 8-hydroxyquinoléine et ses sels, le chlorure de diméthyl alkylbenzylammonium (alkyl est un dérivé d'acide gras de coprah). Ces agents antiseptiques sont présents dans des quantités comprises entre 0,01 et 2,5% en poids par rapport au poids total de la composition. :The antiseptic agents which can be used in this embodiment of the invention are agents known in themselves and commonly used in antiseptic compositions. Mention may be made, for this purpose, of hexamidine diisethionate, 2,4,4'-trichloro-2'-hydroxy-biphenyl ether, chlorhexidine, chlorhexidine digluconate, 4-benzalkonium chloride, 3,4, 4'-trichlorocarbanilide, 8-hydroxyquinoline and its salts, dimethyl alkylbenzylammonium chloride (alkyl is a derivative of coconut fatty acid). These antiseptic agents are present in amounts of between 0.01 and 2.5% by weight relative to the total weight of the composition. :
Les compositions conformes à l'invention se présentent généralement sous forme de compositions aqueuses pouvant éventuellement contenir suivant l'application envisagée des solvants cosmétiquement acceptables et avoir un pH compris entre par exemple 3,5 et 8.The compositions in accordance with the invention are generally in the form of aqueous compositions which may optionally contain, depending on the intended application, cosmetically acceptable solvents and have a pH of between 3.5 and 8, for example.
Ces compositions peuvent en particulier se présenter lorsqu'elles sont utilisées pour le traitement de la peau sous forme de crème, de lait, d'émulsion, de gel, de solution aqueuse ou hydroalcoolique. Elles contiennent en plus des adjuvants tels que des parfums, des colorants, des agents / conservateurs, des agents épaississants, des agents séouesy^/ il / · 8 trants, des agents émulsifiants, des filtres solaires ainsi que tout autre produit bien connu dans l'état de la technique et couramment utilisés pour former des compositions de ce type.These compositions can in particular be presented when they are used for the treatment of the skin in the form of cream, milk, emulsion, gel, aqueous or hydroalcoholic solution. They also contain adjuvants such as perfumes, dyes, agents / preservatives, thickening agents, drying agents, emulsifiers, sunscreens and any other product well known in the art. 'state of the art and commonly used to form compositions of this type.
Les compositions destinées au nettoyage des cheveux =. peuvent se présenter sous forme de solutions aqueuses ou hydroalcooliques, d'émulsions, de crèmes, de lait, de gel et eventuellement être conditionnées en aérosol avec un agent propulseur tel que l'azote, le protoxyde d'azote, les hydrocarbures fluorochlorés du type Fréon ou les hydrocarbures saturés tels que le butane ou le propane.The compositions intended for cleaning the hair logo CNRS logo INIST. may be in the form of aqueous or hydroalcoholic solutions, emulsions, creams, milk, gel and possibly be aerosolized with a propellant such as nitrogen, nitrous oxide, fluorochlorinated hydrocarbons of the type Freon or saturated hydrocarbons such as butane or propane.
Les exemples qui suivent sont destinés à illustrer l'invention sans pour autant présenter un caractère limitatif. / é' ( ♦ * 9 EXEMPLE 1The examples which follow are intended to illustrate the invention without however being limiting in nature. / é '(♦ * 9 EXAMPLE 1
On a préparé la composition suivante : TRITON CG-110-60 8¾ TWEEN 20 2%The following composition was prepared: TRITON CG-110-60 8¾ TWEEN 20 2%
Hydroxyéthylcellulose 0,3% ». Diiséthionate d'hexamidine 0,05%Hydroxyethylcellulose 0.3% ". 0.05% hexamidine diisethionate
Eau q.s.p. 100Water q.s.p. 100
Cette composition est utilisée pour le lavage de la peau.This composition is used for washing the skin.
Le point de demi-lyse est égal à 1,38% et la composition a une détergence équivalente à 3% de laurylsulfate de sodium.The half-lysis point is equal to 1.38% and the composition has a detergency equivalent to 3% of sodium lauryl sulfate.
EXEMPLE 2EXAMPLE 2
On prépare la composition antiseptique suivante : TRITON CG-110-60 8% en M.A.The following antiseptic composition is prepared: TRITON CG-110-60 8% in M.A.
TWEEN 20 2%TWEEN 20 2%
Hydroxyéthylcellulose 0,3%Hydroxyethylcellulose 0.3%
Diiséthionate d'hexamidine 0,15%0.15% hexamidine diisethionate
Irgasan DP 300 0, lO-oIrgasan DP 300 0, lO-o
Eau et conservateur q.s.p. 100Water and preservative q.s.p. 100
Cette composition est utilisée pour le lavage de la peau et a un effet antiseptique. Le point de demi-lyse de la composition est de 1,31% et la composition est équivalente au test de détergence a une solution aqueuse de 2,5% de laurylsulfate de sodium.This composition is used for washing the skin and has an antiseptic effect. The half-lysis point of the composition is 1.31% and the composition is equivalent to the detergency test to an aqueous solution of 2.5% of sodium lauryl sulfate.
EXEMPLE 3EXAMPLE 3
On prépare la composition suivante : TRITON CG-110-60 8% en M.A.The following composition is prepared: TRITON CG-110-60 8% in M.A.
Hydroxyéthylcellulose 0,3%Hydroxyethylcellulose 0.3%
Eau q.s.p. 100.Water q.s.p. 100.
Cette composition est utilisée pour le lavage de la peau.This composition is used for washing the skin.
Le point de demi-lyse est de 1,23% alors qu'une composition aqueuse de laurylsulfate de sodium ayant la même teneur en matière active c'est-à-dire 8,3% a un point de demi-lyse de 0,03%.The half-lysis point is 1.23% while an aqueous composition of sodium lauryl sulphate having the same active ingredient content, that is to say 8.3% has a half-lysis point of 0, 03%.
EXEMPLE 4EXAMPLE 4
On prépare la composition suivante : / / TRITON CG-110-60 8% en M.A// 10The following composition is prepared: / / TRITON CG-110-60 8% in M.A // 10
Poly-/5-alanine telle gue décrite dans l'exemple de référence 1 5% en M.A.Poly- / 5-alanine as described in the reference example 15% in M.A.
Eau q.s.p. 100Water q.s.p. 100
Cette composition est utilisée pour le lavage de la peau. On constate que le point de demi-lyse est de 1,23% de produit alors qu’une composition ayant la même teneur en matière active c’est-à-dire 13% en laurylsulfate de sodium a un point de demi-lyse de 0,014%.This composition is used for washing the skin. It is found that the half-lysis point is 1.23% of product while a composition having the same active ingredient content, that is to say 13% of sodium lauryl sulfate has a half-lysis point of 0.014%.
EXEMPLE 5EXAMPLE 5
On prépare la composition suivante : TRITON CG-110-60 5,78 gThe following composition is prepared: TRITON CG-110-60 5.78 g
Hydroxyéthylcellulose 0,22 gHydroxyethylcellulose 0.22 g
Eau q.s.p. 100 /Water q.s.p. 100 /
Le point de demi-lyse de cette composition est 1,84% de produit. /1·/ il • / 11 EXEMPLE DE REFERENCE A Préparation de la poly-fb-alanine.The half-lysis point of this composition is 1.84% of product. / 1 · / il • / 11 REFERENCE EXAMPLE A Preparation of poly-fb-alanine.
Dans un réacteur de 6 litres, muni d'un agitateur, d'une arrivée d'azote et d'un réfrigérant surmonté d'une garde à chlorure de calcium, on introduit 0,15 g de N-phényl-^^apbtyl-amine et 2,5 litres de chlorobenzène. La solution est alors chauffée à 80°C et l'on ajoute 150 g d'acrylamide. Après dissolution complète du monomère et retour du mélange réactionnel à 80°C, on ajoute une solution chaude de 3 g de sodium préalablement mis en solution dans 300 ml de tertio-butanol.0.15 g of N-phenyl - ^^ apbtyl- is introduced into a 6-liter reactor, fitted with an agitator, a nitrogen inlet and a cooler surmounted by a calcium chloride guard. amine and 2.5 liters of chlorobenzene. The solution is then heated to 80 ° C. and 150 g of acrylamide are added. After complete dissolution of the monomer and return of the reaction mixture at 80 ° C., a hot solution of 3 g of sodium previously dissolved in 300 ml of tert-butanol is added.
Un polymère insoluble dans le milieu réactionnel se forme rapidement et se dépose sur les parois du réacteur. La réaction est maintenue 8 heures à 80°C. En fin de réaction, le solvant est éliminé avant refroidissement et le polymère est alors dissous dans 1350 ml d'eau. La solution obtenue est ajustée à pH 6 par de l'acide chlorhydrigue concentré. La phase aqueuse précédente est lavée par 500 ml de chloroforme, filtrée et concentrée à 1'évaporateur rotatif sous pression réduite jusqu'à l'obtention de 350 g de résidu huileux. Le polymère pur est obtenu en versant lentement le concentrât aqueux dans 15 litres d'éthanol sous vive agitation puis en filtrant la poudre en suspension.A polymer insoluble in the reaction medium quickly forms and is deposited on the walls of the reactor. The reaction is maintained for 8 hours at 80 ° C. At the end of the reaction, the solvent is removed before cooling and the polymer is then dissolved in 1350 ml of water. The solution obtained is adjusted to pH 6 with concentrated hydrochloric acid. The above aqueous phase is washed with 500 ml of chloroform, filtered and concentrated on a rotary evaporator under reduced pressure until 350 g of oily residue is obtained. The pure polymer is obtained by slowly pouring the aqueous concentrate into 15 liters of ethanol with vigorous stirring and then filtering the powder in suspension.
On obtient ainsi après séchage 135 g d'une poudre blanche soit un rendement de 90%.135 g of a white powder are thus obtained after drying, ie a yield of 90%.
//
Viscosité : intrinsèque dans l'eau à 25°C :. / £n J = 0,121dl/g. ^ *Viscosity: intrinsic in water at 25 ° C:. / £ n J = 0.121dl / g. ^ *
Claims (13)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU84416A LU84416A1 (en) | 1982-10-11 | 1982-10-11 | SOFT CLEANING COMPOSITION |
| CA000438406A CA1205747A (en) | 1982-10-11 | 1983-10-05 | Soft cleansing compound |
| ES526357A ES8601682A1 (en) | 1982-10-11 | 1983-10-10 | Mild cleaning composition |
| BE0/211680A BE897961A (en) | 1982-10-11 | 1983-10-10 | SOFT CLEANING COMPOSITION |
| GB08327031A GB2128627B (en) | 1982-10-11 | 1983-10-10 | Mild cleaning compostion |
| DE19833336760 DE3336760A1 (en) | 1982-10-11 | 1983-10-10 | Mild CLEANING COMPOSITION |
| FR8316085A FR2534270B1 (en) | 1982-10-11 | 1983-10-10 | SOFT CLEANING COMPOSITION |
| NL8303471A NL8303471A (en) | 1982-10-11 | 1983-10-10 | MILD CLEANER. |
| IT68037/83A IT1160211B (en) | 1982-10-11 | 1983-10-10 | SWEET WASHING COMPOSITION PARTICULARLY FOR WASHING HAIR AND SKIN |
| JP58189779A JPS59130210A (en) | 1982-10-11 | 1983-10-11 | mild cleaning composition |
| CH5532/83A CH658991A5 (en) | 1982-10-11 | 1983-10-11 | COSMETIC COMPOSITION FOR SOFT CLEANING. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU84416A LU84416A1 (en) | 1982-10-11 | 1982-10-11 | SOFT CLEANING COMPOSITION |
| LU84416 | 1982-10-11 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU84416A1 true LU84416A1 (en) | 1984-05-10 |
Family
ID=19729963
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU84416A LU84416A1 (en) | 1982-10-11 | 1982-10-11 | SOFT CLEANING COMPOSITION |
Country Status (11)
| Country | Link |
|---|---|
| JP (1) | JPS59130210A (en) |
| BE (1) | BE897961A (en) |
| CA (1) | CA1205747A (en) |
| CH (1) | CH658991A5 (en) |
| DE (1) | DE3336760A1 (en) |
| ES (1) | ES8601682A1 (en) |
| FR (1) | FR2534270B1 (en) |
| GB (1) | GB2128627B (en) |
| IT (1) | IT1160211B (en) |
| LU (1) | LU84416A1 (en) |
| NL (1) | NL8303471A (en) |
Families Citing this family (30)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2553660B1 (en) * | 1983-10-25 | 1986-01-03 | Oreal | COSMETIC CLEANING COMPOSITION IN PARTICULAR FOR EYE MAKE-UP REMOVAL |
| LU85111A1 (en) * | 1983-12-01 | 1985-09-12 | Oreal | ANTI-ACNETIC COMPOSITION BASED ON BENZOYL PEROXIDE AND AT LEAST ONE SOLAR FILTER |
| FR2564318B1 (en) * | 1984-05-15 | 1987-04-17 | Oreal | ANHYDROUS COMPOSITION FOR CLEANING THE SKIN |
| LU85427A1 (en) | 1984-06-22 | 1986-01-24 | Oreal | NOVEL COMPOSITIONS FOR DELAYING THE APPEARANCE OF A FATTY ASPECT OF THE HAIR, AND USE THEREOF |
| FR2589356B1 (en) * | 1985-10-31 | 1988-11-25 | Oreal | SOFT CLEANING COSMETIC COMPOSITION, PARTICULARLY FOR EYE MAKE-UP REMOVAL |
| JP2534633B2 (en) * | 1987-07-20 | 1996-09-18 | 鐘紡株式会社 | Skin cosmetics for clean room |
| MY105119A (en) * | 1988-04-12 | 1994-08-30 | Kao Corp | Low irritation detergent composition. |
| LU87323A1 (en) * | 1988-08-25 | 1990-03-13 | Oreal | COMPOSITION FOR INDUCING AND STIMULATING HAIR GROWTH AND / OR BRAKING HAIR LOSS, BASED ON ALKYLPOLYGLYCOSIDE AND A PYRIMIDINE DERIVATIVE |
| JPH0768115B2 (en) * | 1989-05-17 | 1995-07-26 | 花王株式会社 | Cleaning composition |
| US5234618A (en) * | 1989-10-09 | 1993-08-10 | Kao Corporation | Liquid detergent composition |
| JPH0623087B2 (en) * | 1989-10-09 | 1994-03-30 | 花王株式会社 | Cleaning composition |
| GB8927956D0 (en) * | 1989-12-11 | 1990-02-14 | Unilever Plc | Detergent composition |
| FR2660552B1 (en) * | 1990-04-06 | 1994-09-02 | Rhone Poulenc Sante | NEW ANTISEPTIC DRUGS. |
| US5690920A (en) * | 1990-11-15 | 1997-11-25 | L'oreal | Foamable washing composition based on selected insoluble silicones and an alkylpolyglycoside, and cosmetic and dermatological uses thereof |
| FR2669345B1 (en) * | 1990-11-15 | 1994-08-26 | Oreal | CLEANSING AND FOAMING COMPOSITION BASED ON INSOLUBLE SILICONES AND AN ALKYLPOLYGLYCOSIDE AND THEIR APPLICATION IN COSMETICS AND DERMATOLOGY. |
| US5246695A (en) * | 1991-04-03 | 1993-09-21 | Rewo Chemische Werke Gmbh | Use of alkylglycoside sulfosuccinates for the production of cosmetic preparations and cleaning agents |
| DE4110663A1 (en) * | 1991-04-03 | 1992-10-08 | Rewo Chemische Werke Gmbh | NEW AMMONIUM COMPOUNDS, PROCESS FOR THEIR PREPARATION AND THEIR USE AS CLEANING AGENTS, COSMETIC RAW MATERIALS AND SOFTWARE, IN PARTICULAR AS SOFTENER SPILLS FOR TISSUE |
| FR2680103B1 (en) * | 1991-08-07 | 1993-10-29 | Oreal | USE IN COSMETICS OR IN PHARMACY OF ALKYLPOLYGLYCOSIDES AND / OR GLUCOSE O-ACYLATED DERIVATIVES FOR THE TREATMENT OF HAIR LOSS. |
| EP0538762B1 (en) * | 1991-10-22 | 1996-04-10 | Kao Corporation | Hair cosmetic |
| FR2687069B1 (en) * | 1992-02-07 | 1995-06-09 | Oreal | COSMETIC COMPOSITION CONTAINING AT LEAST ONE SURFACTANT AGENT OF THE ALKYLPOLYGLYCOSIDE AND / OR POLYGLYCEROLE TYPE AND AT LEAST ONE URETHANE POLYETHER. |
| DE4302315A1 (en) * | 1993-01-28 | 1994-08-04 | Henkel Kgaa | Surface active mixtures |
| DE4319699A1 (en) * | 1993-06-16 | 1994-12-22 | Henkel Kgaa | Ultra mild surfactant blends |
| DE4319700A1 (en) * | 1993-06-16 | 1994-12-22 | Henkel Kgaa | Ultra mild surfactant blends |
| AU7920394A (en) * | 1993-10-06 | 1995-05-01 | Henkel Corporation | Improving phenolic disinfectant cleaning compositions with alkylpolyglucoside surfactants |
| US5681802A (en) * | 1994-06-01 | 1997-10-28 | Lever Brothers Company, Division Of Conopco, Inc. | Mild antimicrobial liquid cleansing formulations comprising buffering compound or compounds as potentiator of antimicrobial effectiveness |
| US5728371A (en) * | 1996-04-29 | 1998-03-17 | L'oreal, S.A. | Skin protection, fragrance enhancing and vitamin delivery composition |
| US5728372A (en) * | 1996-04-29 | 1998-03-17 | L'oreal, S.A. | Skin protection, fragrance enhancing and vitamin delivery composition |
| DE19723733A1 (en) | 1997-06-06 | 1998-12-10 | Beiersdorf Ag | Cosmetic and dermatological emulsions containing alkyl glucosides and increased electrolyte concentrations |
| DE10154628A1 (en) * | 2001-09-25 | 2003-04-10 | Beiersdorf Ag | Surfactant(s) for use in cosmetic or dermatological cleaning, comprise alkyl glucosides |
| JP6177634B2 (en) * | 2013-09-13 | 2017-08-09 | クラシエホームプロダクツ株式会社 | Skin cleanser composition |
Family Cites Families (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU60900A1 (en) * | 1970-05-12 | 1972-02-10 | ||
| SE7407206L (en) * | 1973-06-04 | 1974-12-05 | Tennant Co | |
| US4154706A (en) * | 1976-07-23 | 1979-05-15 | Colgate-Palmolive Company | Nonionic shampoo |
| FR2397185A1 (en) * | 1977-05-18 | 1979-02-09 | Oreal | NON-IRRITANT COMPOSITION FOR EYE MAKE-UP REMOVAL |
| FR2413084A1 (en) * | 1977-12-30 | 1979-07-27 | Oreal | COSMETIC COMPOSITION FOR EYE MAKE-UP REMOVAL |
| LU81257A1 (en) * | 1979-05-15 | 1980-12-16 | Oreal | COSMETIC COMPOSITION FOR THE TREATMENT OF HAIR AND SKIN, CONTAINING SALSEPAREILLE EXTRACT |
| FR2508795A1 (en) * | 1981-07-03 | 1983-01-07 | Oreal | COSMETIC COMPOSITIONS FOR THE TREATMENT OF HAIR AND SKIN CONTAINING POLYAMIDES |
-
1982
- 1982-10-11 LU LU84416A patent/LU84416A1/en unknown
-
1983
- 1983-10-05 CA CA000438406A patent/CA1205747A/en not_active Expired
- 1983-10-10 BE BE0/211680A patent/BE897961A/en not_active IP Right Cessation
- 1983-10-10 FR FR8316085A patent/FR2534270B1/en not_active Expired
- 1983-10-10 DE DE19833336760 patent/DE3336760A1/en active Granted
- 1983-10-10 NL NL8303471A patent/NL8303471A/en not_active Application Discontinuation
- 1983-10-10 IT IT68037/83A patent/IT1160211B/en active
- 1983-10-10 GB GB08327031A patent/GB2128627B/en not_active Expired
- 1983-10-10 ES ES526357A patent/ES8601682A1/en not_active Expired
- 1983-10-11 CH CH5532/83A patent/CH658991A5/en not_active IP Right Cessation
- 1983-10-11 JP JP58189779A patent/JPS59130210A/en active Granted
Also Published As
| Publication number | Publication date |
|---|---|
| FR2534270B1 (en) | 1986-07-04 |
| JPS59130210A (en) | 1984-07-26 |
| NL8303471A (en) | 1984-05-01 |
| JPH0336804B2 (en) | 1991-06-03 |
| CA1205747A (en) | 1986-06-10 |
| ES526357A0 (en) | 1985-11-16 |
| GB8327031D0 (en) | 1983-11-09 |
| ES8601682A1 (en) | 1985-11-16 |
| IT1160211B (en) | 1987-03-04 |
| BE897961A (en) | 1984-04-10 |
| GB2128627A (en) | 1984-05-02 |
| GB2128627B (en) | 1987-01-14 |
| DE3336760A1 (en) | 1984-04-12 |
| DE3336760C2 (en) | 1991-11-14 |
| CH658991A5 (en) | 1986-12-31 |
| FR2534270A1 (en) | 1984-04-13 |
| IT8368037A0 (en) | 1983-10-10 |
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