LU83350A1 - Composition destinee au traitement des fibres keratiniques a base de polymere cationique et de polymere anionique a groupements vinylsulfoniques et procede de traitement la mettant en oeuvre - Google Patents
Composition destinee au traitement des fibres keratiniques a base de polymere cationique et de polymere anionique a groupements vinylsulfoniques et procede de traitement la mettant en oeuvre Download PDFInfo
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- LU83350A1 LU83350A1 LU83350A LU83350A LU83350A1 LU 83350 A1 LU83350 A1 LU 83350A1 LU 83350 A LU83350 A LU 83350A LU 83350 A LU83350 A LU 83350A LU 83350 A1 LU83350 A1 LU 83350A1
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- 239000000203 mixture Substances 0.000 title claims description 111
- 229920006318 anionic polymer Polymers 0.000 title claims description 30
- 229920006317 cationic polymer Polymers 0.000 title claims description 29
- 238000000034 method Methods 0.000 title claims description 16
- 239000000835 fiber Substances 0.000 title description 12
- 229920000642 polymer Polymers 0.000 claims description 74
- -1 saturated aliphatic dicarbo-xylic acids Chemical class 0.000 claims description 43
- 125000000217 alkyl group Chemical group 0.000 claims description 33
- 125000004432 carbon atom Chemical group C* 0.000 claims description 23
- 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 claims description 21
- 239000004952 Polyamide Substances 0.000 claims description 21
- 229920001577 copolymer Polymers 0.000 claims description 21
- 229920002647 polyamide Polymers 0.000 claims description 21
- 239000011734 sodium Substances 0.000 claims description 21
- 229910052708 sodium Inorganic materials 0.000 claims description 21
- 125000002091 cationic group Chemical group 0.000 claims description 19
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 19
- 150000001875 compounds Chemical class 0.000 claims description 18
- 229920002554 vinyl polymer Polymers 0.000 claims description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 18
- 125000003277 amino group Chemical group 0.000 claims description 17
- 239000006210 lotion Substances 0.000 claims description 17
- 229920000768 polyamine Polymers 0.000 claims description 16
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 229910052757 nitrogen Inorganic materials 0.000 claims description 15
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- 239000002253 acid Substances 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 14
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 13
- 239000000178 monomer Substances 0.000 claims description 13
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 13
- 239000000975 dye Substances 0.000 claims description 11
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- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 claims description 10
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 claims description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 10
- 239000000463 material Substances 0.000 claims description 10
- 230000008569 process Effects 0.000 claims description 10
- 229920001281 polyalkylene Polymers 0.000 claims description 9
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical group C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 claims description 8
- 238000004132 cross linking Methods 0.000 claims description 8
- 239000003431 cross linking reagent Substances 0.000 claims description 8
- 150000002148 esters Chemical class 0.000 claims description 8
- 229930195733 hydrocarbon Natural products 0.000 claims description 8
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 7
- 150000007513 acids Chemical class 0.000 claims description 7
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- 239000003795 chemical substances by application Substances 0.000 claims description 7
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- FQPSGWSUVKBHSU-UHFFFAOYSA-N methacrylamide Chemical compound CC(=C)C(N)=O FQPSGWSUVKBHSU-UHFFFAOYSA-N 0.000 claims description 7
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 claims description 6
- 239000004215 Carbon black (E152) Substances 0.000 claims description 6
- 239000000443 aerosol Substances 0.000 claims description 6
- 125000000129 anionic group Chemical group 0.000 claims description 6
- 150000001450 anions Chemical class 0.000 claims description 6
- 125000000623 heterocyclic group Chemical group 0.000 claims description 6
- 125000001453 quaternary ammonium group Chemical group 0.000 claims description 6
- 150000003335 secondary amines Chemical group 0.000 claims description 6
- 239000002904 solvent Substances 0.000 claims description 6
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 5
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical compound C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 claims description 5
- 229910052784 alkaline earth metal Inorganic materials 0.000 claims description 5
- 238000005804 alkylation reaction Methods 0.000 claims description 5
- 229910052799 carbon Inorganic materials 0.000 claims description 5
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 5
- 239000006260 foam Substances 0.000 claims description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 5
- 238000006068 polycondensation reaction Methods 0.000 claims description 5
- 239000002562 thickening agent Substances 0.000 claims description 5
- CPELXLSAUQHCOX-UHFFFAOYSA-M Bromide Chemical compound [Br-] CPELXLSAUQHCOX-UHFFFAOYSA-M 0.000 claims description 4
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 4
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 claims description 4
- 150000003926 acrylamides Chemical class 0.000 claims description 4
- 230000029936 alkylation Effects 0.000 claims description 4
- 125000002947 alkylene group Chemical group 0.000 claims description 4
- 125000003118 aryl group Chemical group 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 4
- 230000001588 bifunctional effect Effects 0.000 claims description 4
- 238000006243 chemical reaction Methods 0.000 claims description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N hexanedioic acid Natural products OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 4
- 229920001519 homopolymer Polymers 0.000 claims description 4
- 150000002431 hydrogen Chemical class 0.000 claims description 4
- 125000002768 hydroxyalkyl group Chemical group 0.000 claims description 4
- 238000006116 polymerization reaction Methods 0.000 claims description 4
- 239000000843 powder Substances 0.000 claims description 4
- 150000003141 primary amines Chemical group 0.000 claims description 4
- 229920006395 saturated elastomer Polymers 0.000 claims description 4
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 3
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical group C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims description 3
- 239000005977 Ethylene Substances 0.000 claims description 3
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 3
- 239000001361 adipic acid Substances 0.000 claims description 3
- 235000011037 adipic acid Nutrition 0.000 claims description 3
- 239000002671 adjuvant Substances 0.000 claims description 3
- 125000001931 aliphatic group Chemical group 0.000 claims description 3
- 239000003513 alkali Substances 0.000 claims description 3
- 150000001342 alkaline earth metals Chemical class 0.000 claims description 3
- 150000003973 alkyl amines Chemical class 0.000 claims description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 3
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 3
- 239000011575 calcium Substances 0.000 claims description 3
- 229910052791 calcium Inorganic materials 0.000 claims description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 3
- 239000001913 cellulose Substances 0.000 claims description 3
- 229920002678 cellulose Polymers 0.000 claims description 3
- 239000006071 cream Substances 0.000 claims description 3
- 150000002466 imines Chemical class 0.000 claims description 3
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 claims description 3
- 150000007524 organic acids Chemical class 0.000 claims description 3
- 230000003647 oxidation Effects 0.000 claims description 3
- 238000007254 oxidation reaction Methods 0.000 claims description 3
- 239000001301 oxygen Substances 0.000 claims description 3
- 229910052760 oxygen Inorganic materials 0.000 claims description 3
- 239000011591 potassium Substances 0.000 claims description 3
- 229910052700 potassium Inorganic materials 0.000 claims description 3
- 238000005956 quaternization reaction Methods 0.000 claims description 3
- 125000004434 sulfur atom Chemical group 0.000 claims description 3
- 229920001567 vinyl ester resin Polymers 0.000 claims description 3
- OSSNTDFYBPYIEC-UHFFFAOYSA-N 1-ethenylimidazole Chemical compound C=CN1C=CN=C1 OSSNTDFYBPYIEC-UHFFFAOYSA-N 0.000 claims description 2
- WDRZVZVXHZNSFG-UHFFFAOYSA-N 1-ethenylpyridin-1-ium Chemical group C=C[N+]1=CC=CC=C1 WDRZVZVXHZNSFG-UHFFFAOYSA-N 0.000 claims description 2
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 claims description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 claims description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-M Bisulfite Chemical compound OS([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-M 0.000 claims description 2
- BTBUEUYNUDRHOZ-UHFFFAOYSA-N Borate Chemical compound [O-]B([O-])[O-] BTBUEUYNUDRHOZ-UHFFFAOYSA-N 0.000 claims description 2
- 229920002101 Chitin Polymers 0.000 claims description 2
- KRKNYBCHXYNGOX-UHFFFAOYSA-K Citrate Chemical compound [O-]C(=O)CC(O)(CC([O-])=O)C([O-])=O KRKNYBCHXYNGOX-UHFFFAOYSA-K 0.000 claims description 2
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 claims description 2
- QEVGZEDELICMKH-UHFFFAOYSA-N Diglycolic acid Chemical compound OC(=O)COCC(O)=O QEVGZEDELICMKH-UHFFFAOYSA-N 0.000 claims description 2
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical compound CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims description 2
- 229910019142 PO4 Inorganic materials 0.000 claims description 2
- QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 2
- 230000001476 alcoholic effect Effects 0.000 claims description 2
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 230000002152 alkylating effect Effects 0.000 claims description 2
- 150000003863 ammonium salts Chemical class 0.000 claims description 2
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- 239000000470 constituent Substances 0.000 claims description 2
- 125000004427 diamine group Chemical group 0.000 claims description 2
- 239000003792 electrolyte Substances 0.000 claims description 2
- GMQPCAHXQLIQLH-UHFFFAOYSA-N ethenyl 3-(2-oxopyrrolidin-1-yl)prop-2-enoate Chemical compound C=COC(=O)C=CN1CCCC1=O GMQPCAHXQLIQLH-UHFFFAOYSA-N 0.000 claims description 2
- 239000004872 foam stabilizing agent Substances 0.000 claims description 2
- 125000003827 glycol group Chemical group 0.000 claims description 2
- 125000005842 heteroatom Chemical group 0.000 claims description 2
- QAOWNCQODCNURD-UHFFFAOYSA-M hydrogensulfate Chemical compound OS([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-M 0.000 claims description 2
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
- 229910052500 inorganic mineral Inorganic materials 0.000 claims description 2
- 239000011707 mineral Substances 0.000 claims description 2
- 239000002736 nonionic surfactant Substances 0.000 claims description 2
- 125000004430 oxygen atom Chemical group O* 0.000 claims description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 claims description 2
- 239000010452 phosphate Substances 0.000 claims description 2
- 150000004885 piperazines Chemical class 0.000 claims description 2
- 229920001282 polysaccharide Polymers 0.000 claims description 2
- 239000005017 polysaccharide Substances 0.000 claims description 2
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- 239000003352 sequestering agent Substances 0.000 claims description 2
- 229920005573 silicon-containing polymer Polymers 0.000 claims description 2
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- 229940095064 tartrate Drugs 0.000 claims description 2
- 150000003512 tertiary amines Chemical group 0.000 claims description 2
- GQWWGRUJOCIUKI-UHFFFAOYSA-N 2-[3-(2-methyl-1-oxopyrrolo[1,2-a]pyrazin-3-yl)propyl]guanidine Chemical group O=C1N(C)C(CCCN=C(N)N)=CN2C=CC=C21 GQWWGRUJOCIUKI-UHFFFAOYSA-N 0.000 claims 1
- 150000001340 alkali metals Chemical class 0.000 claims 1
- 229960003237 betaine Drugs 0.000 claims 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 claims 1
- 125000006159 dianhydride group Chemical group 0.000 claims 1
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- 230000000475 sunscreen effect Effects 0.000 claims 1
- 239000000516 sunscreening agent Substances 0.000 claims 1
- NLVXSWCKKBEXTG-UHFFFAOYSA-N vinylsulfonic acid Chemical compound OS(=O)(=O)C=C NLVXSWCKKBEXTG-UHFFFAOYSA-N 0.000 claims 1
- 210000004209 hair Anatomy 0.000 description 34
- 239000002453 shampoo Substances 0.000 description 17
- FAPWRFPIFSIZLT-UHFFFAOYSA-M Sodium chloride Chemical compound [Na+].[Cl-] FAPWRFPIFSIZLT-UHFFFAOYSA-M 0.000 description 16
- 150000003254 radicals Chemical class 0.000 description 13
- 239000000047 product Substances 0.000 description 12
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 10
- 102000011782 Keratins Human genes 0.000 description 8
- 108010076876 Keratins Proteins 0.000 description 8
- 239000011780 sodium chloride Substances 0.000 description 8
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 7
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- 150000003839 salts Chemical class 0.000 description 7
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- 150000001408 amides Chemical class 0.000 description 5
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- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 5
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- 201000006747 infectious mononucleosis Diseases 0.000 description 5
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- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
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- 238000002360 preparation method Methods 0.000 description 4
- 229940006186 sodium polystyrene sulfonate Drugs 0.000 description 4
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 3
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- 206010019049 Hair texture abnormal Diseases 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
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- 239000007864 aqueous solution Substances 0.000 description 3
- HONIICLYMWZJFZ-UHFFFAOYSA-O azetidin-1-ium Chemical compound C1C[NH2+]C1 HONIICLYMWZJFZ-UHFFFAOYSA-O 0.000 description 3
- 238000004040 coloring Methods 0.000 description 3
- GQOKIYDTHHZSCJ-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;chloride Chemical compound [Cl-].C=CC[N+](C)(C)CC=C GQOKIYDTHHZSCJ-UHFFFAOYSA-M 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
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- DDMOUSALMHHKOS-UHFFFAOYSA-N 1,2-dichloro-1,1,2,2-tetrafluoroethane Chemical compound FC(F)(Cl)C(F)(F)Cl DDMOUSALMHHKOS-UHFFFAOYSA-N 0.000 description 2
- QLAJNZSPVITUCQ-UHFFFAOYSA-N 1,3,2-dioxathietane 2,2-dioxide Chemical compound O=S1(=O)OCO1 QLAJNZSPVITUCQ-UHFFFAOYSA-N 0.000 description 2
- 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 2
- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
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- FOCAUTSVDIKZOP-UHFFFAOYSA-N chloroacetic acid Chemical compound OC(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-N 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 239000002537 cosmetic Substances 0.000 description 2
- ZRKZFNZPJKEWPC-UHFFFAOYSA-N decylamine-N,N-dimethyl-N-oxide Chemical compound CCCCCCCCCC[N+](C)(C)[O-] ZRKZFNZPJKEWPC-UHFFFAOYSA-N 0.000 description 2
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 2
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 2
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 description 2
- 239000004664 distearyldimethylammonium chloride (DHTDMAC) Substances 0.000 description 2
- NAQMVNRVTILPCV-UHFFFAOYSA-N hexane-1,6-diamine Chemical compound NCCCCCCN NAQMVNRVTILPCV-UHFFFAOYSA-N 0.000 description 2
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- 239000004615 ingredient Substances 0.000 description 2
- NNPPMTNAJDCUHE-UHFFFAOYSA-N isobutane Chemical compound CC(C)C NNPPMTNAJDCUHE-UHFFFAOYSA-N 0.000 description 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
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- 229960002796 polystyrene sulfonate Drugs 0.000 description 2
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 2
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Classifications
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- Compositions Of Macromolecular Compounds (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Detergent Compositions (AREA)
Priority Applications (14)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
LU83350A LU83350A1 (fr) | 1981-05-08 | 1981-05-08 | Composition destinee au traitement des fibres keratiniques a base de polymere cationique et de polymere anionique a groupements vinylsulfoniques et procede de traitement la mettant en oeuvre |
DE3216687A DE3216687C2 (de) | 1981-05-08 | 1982-05-04 | Mittel zur Behandlung keratinischer Substanzen und seine Verwendung |
DK204282A DK204282A (da) | 1981-05-08 | 1982-05-06 | Middel paa basis af kationiske polymere og anioniske polymere indeholdende vinylsulfonsyregrupper og fremgangsmaade til behandling af keratinfibre under anvendelse af midlet |
GB8213081A GB2098226B (en) | 1981-05-08 | 1982-05-06 | Composition intended for the treatment of keratin fibres based on a cationic polymer and ananionic polymer containing vinylsulphonic groups |
SE8202843A SE8202843L (sv) | 1981-05-08 | 1982-05-06 | Komposition baserad pa katjonisk och anjonisk polymer med vinylsulfongrupper avsedd for behandling av keratinfibrer samt behandlingsforfarande derfor |
CA000402538A CA1179268A (fr) | 1981-05-08 | 1982-05-07 | Composition destinee au traitement des fibres keratiniques a base de polymere cationique et de polymere anionique a groupements vinylsulfoniques et procede de traitement la mettant en oeuvre |
BE0/208034A BE893113A (fr) | 1981-05-08 | 1982-05-07 | Composition destinee au traitement des fibres keratiniques a base de polymere cationique et de polymere anionique a groupements vinylsulfoniques |
CH2873/82A CH652920A5 (fr) | 1981-05-08 | 1982-05-07 | Procede de traitement des fibres keratiniques a l'aide de polymere cationique et de polymere anionique a groupements vinylsulfoniques et composition pour la mise en oeuvre du procede. |
AT0180482A AT378910B (de) | 1981-05-08 | 1982-05-07 | Verfahren und mittel zur behandlung keratinischer substanzen |
JP57076490A JPS57198800A (en) | 1981-05-08 | 1982-05-07 | Composition for keratin fiber treatment and treating process |
IT67604/82A IT1157009B (it) | 1981-05-08 | 1982-05-07 | Composizione per il trattamento di fibre cheratiniche a base di polimero cationico e di polimero anionico con gruppi vinilsolfonici e procedimento di trattamento mediante tale composizione |
NL8201877A NL8201877A (nl) | 1981-05-08 | 1982-05-07 | Produkt, bestemd voor het behandelen van keratinevezels, op basis van kationogeen polymeer en anionogeen polymeer met vinylsulfonzuurgroepen en behandelingswerkwijze onder toepassing van dit produkt. |
FR8207997A FR2505179B1 (fr) | 1981-05-08 | 1982-05-07 | Composition destinee au traitement des fibres keratiniques a base de polymere cationique et de polymere anionique a groupements vinylsulfoniques et procede de traitement la mettant en oeuvre |
US07/115,612 US4842849A (en) | 1981-05-08 | 1987-10-30 | Composition intended for the treatment of keratin fibres, based on a cationic polymer and an anionic polymer containing vinylsulphonic groups |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
LU83350A LU83350A1 (fr) | 1981-05-08 | 1981-05-08 | Composition destinee au traitement des fibres keratiniques a base de polymere cationique et de polymere anionique a groupements vinylsulfoniques et procede de traitement la mettant en oeuvre |
LU83350 | 1981-05-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
LU83350A1 true LU83350A1 (fr) | 1983-03-24 |
Family
ID=19729648
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
LU83350A LU83350A1 (fr) | 1981-05-08 | 1981-05-08 | Composition destinee au traitement des fibres keratiniques a base de polymere cationique et de polymere anionique a groupements vinylsulfoniques et procede de traitement la mettant en oeuvre |
Country Status (14)
Country | Link |
---|---|
US (1) | US4842849A (en, 2012) |
JP (1) | JPS57198800A (en, 2012) |
AT (1) | AT378910B (en, 2012) |
BE (1) | BE893113A (en, 2012) |
CA (1) | CA1179268A (en, 2012) |
CH (1) | CH652920A5 (en, 2012) |
DE (1) | DE3216687C2 (en, 2012) |
DK (1) | DK204282A (en, 2012) |
FR (1) | FR2505179B1 (en, 2012) |
GB (1) | GB2098226B (en, 2012) |
IT (1) | IT1157009B (en, 2012) |
LU (1) | LU83350A1 (en, 2012) |
NL (1) | NL8201877A (en, 2012) |
SE (1) | SE8202843L (en, 2012) |
Families Citing this family (71)
Publication number | Priority date | Publication date | Assignee | Title |
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JPS5813700A (ja) * | 1981-07-17 | 1983-01-26 | 花王株式会社 | 食器用洗浄剤組成物 |
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US4528111A (en) * | 1983-12-22 | 1985-07-09 | Colgate-Palmolive Company | Shaving cream gel containing interpolymer reaction product of selected cationic polymers and anionic polymers |
US4501834A (en) * | 1983-12-22 | 1985-02-26 | Colgate-Palmolive Company | Gels formed from anionic and cationic polymers |
DE3401037A1 (de) * | 1984-01-13 | 1985-07-18 | Wella Ag, 6100 Darmstadt | Mittel zur festigung der frisur und pflege des haares |
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USRE34584E (en) | 1984-11-09 | 1994-04-12 | The Procter & Gamble Company | Shampoo compositions |
FR2600249B2 (fr) * | 1985-07-03 | 1988-09-16 | Oreal | Utilisation de condensats de type amide-amine pour la protection des cheveux contre les agressions atmospheriques, et en particulier contre la lumiere et procede de protection des cheveux |
FR2584292B1 (fr) * | 1985-07-03 | 1987-10-16 | Oreal | Composition cosmetique contenant un condensat du type amide-amine |
LU86429A1 (fr) * | 1986-05-16 | 1987-12-16 | Oreal | Compositions cosmetiques renfermant un polymere cationique et un polymere anionique comme agent epaississant |
JP2651918B2 (ja) * | 1988-02-23 | 1997-09-10 | 三菱化学株式会社 | ゲル状整髪剤組成物 |
US5866104A (en) * | 1988-08-01 | 1999-02-02 | Cataneo; Robert | Nail polish remover |
JPH06503574A (ja) * | 1990-12-05 | 1994-04-21 | ザ、プロクター、エンド、ギャンブル、カンパニー | シリコーン及びカチオン系有機ポリマーコンディショニング剤を含有したシャンプー組成物 |
TW199103B (en, 2012) * | 1991-02-15 | 1993-02-01 | Shiseido Co Ltd | |
NZ243273A (en) * | 1991-06-28 | 1995-02-24 | Calgon Corp | Hair care compositions comprising ampholytic terpolymers |
NZ243274A (en) * | 1991-06-28 | 1994-12-22 | Calgon Corp | Hair care compositions containing ampholytic terpolymers |
NZ243275A (en) * | 1991-06-28 | 1995-03-28 | Calgon Corp | Hair care compositions comprising ampholytic terpolymers |
FR2679444B1 (fr) * | 1991-07-25 | 1995-04-07 | Oreal | Utilisation comme agents epaississants des huiles, dans une composition cosmetique huileuse, d'une association de deux copolymeres. |
AU2502892A (en) * | 1991-08-19 | 1993-03-16 | Procter & Gamble Company, The | Hair spray compositions with ionic styling polymer |
DE69322062T2 (de) * | 1992-07-16 | 1999-07-15 | National Starch And Chemical Investment Holding Corp., Wilmington, Del. | Emulsionspolymere und ihre verwendung in haarfestigungszubereitungen |
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US5338541A (en) * | 1992-10-15 | 1994-08-16 | Calgon Corporation | Dual cationic terpolymers providing superior conditioning properties in hair, skin and nail care products |
DE4302315A1 (de) * | 1993-01-28 | 1994-08-04 | Henkel Kgaa | Oberflächenaktive Mischungen |
FR2715064B1 (fr) * | 1994-01-14 | 1996-02-09 | Oreal | Compositions cosmétiques en aérosol, aérosols les contenant et utilisations. |
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-
1981
- 1981-05-08 LU LU83350A patent/LU83350A1/fr unknown
-
1982
- 1982-05-04 DE DE3216687A patent/DE3216687C2/de not_active Expired - Lifetime
- 1982-05-06 DK DK204282A patent/DK204282A/da unknown
- 1982-05-06 SE SE8202843A patent/SE8202843L/xx not_active Application Discontinuation
- 1982-05-06 GB GB8213081A patent/GB2098226B/en not_active Expired
- 1982-05-07 IT IT67604/82A patent/IT1157009B/it active
- 1982-05-07 CH CH2873/82A patent/CH652920A5/fr not_active IP Right Cessation
- 1982-05-07 NL NL8201877A patent/NL8201877A/nl not_active Application Discontinuation
- 1982-05-07 FR FR8207997A patent/FR2505179B1/fr not_active Expired
- 1982-05-07 CA CA000402538A patent/CA1179268A/fr not_active Expired
- 1982-05-07 AT AT0180482A patent/AT378910B/de not_active IP Right Cessation
- 1982-05-07 BE BE0/208034A patent/BE893113A/fr not_active IP Right Cessation
- 1982-05-07 JP JP57076490A patent/JPS57198800A/ja active Granted
-
1987
- 1987-10-30 US US07/115,612 patent/US4842849A/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
FR2505179B1 (fr) | 1987-10-23 |
JPH04961B2 (en, 2012) | 1992-01-09 |
NL8201877A (nl) | 1982-12-01 |
JPS57198800A (en) | 1982-12-06 |
DE3216687C2 (de) | 1996-07-18 |
SE8202843L (sv) | 1982-11-09 |
FR2505179A1 (fr) | 1982-11-12 |
US4842849A (en) | 1989-06-27 |
GB2098226A (en) | 1982-11-17 |
IT1157009B (it) | 1987-02-11 |
CA1179268A (fr) | 1984-12-11 |
DK204282A (da) | 1982-11-09 |
CH652920A5 (fr) | 1985-12-13 |
BE893113A (fr) | 1982-11-08 |
DE3216687A1 (de) | 1982-12-02 |
IT8267604A0 (it) | 1982-05-07 |
AT378910B (de) | 1985-10-25 |
ATA180482A (de) | 1985-03-15 |
GB2098226B (en) | 1984-11-28 |
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