SE461436B - Foerfarande foer lockpermanentning eller rakpermanentning av haar jaemte permanentningskomposition foer anvaendning vid naemnda foerfarande - Google Patents
Foerfarande foer lockpermanentning eller rakpermanentning av haar jaemte permanentningskomposition foer anvaendning vid naemnda foerfarandeInfo
- Publication number
- SE461436B SE461436B SE8300626A SE8300626A SE461436B SE 461436 B SE461436 B SE 461436B SE 8300626 A SE8300626 A SE 8300626A SE 8300626 A SE8300626 A SE 8300626A SE 461436 B SE461436 B SE 461436B
- Authority
- SE
- Sweden
- Prior art keywords
- hair
- composition
- weight
- permanent
- lotion
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims description 25
- 238000000034 method Methods 0.000 title claims description 18
- 210000004209 hair Anatomy 0.000 claims description 63
- 230000003472 neutralizing effect Effects 0.000 claims description 26
- 229920006317 cationic polymer Polymers 0.000 claims description 17
- 239000003638 chemical reducing agent Substances 0.000 claims description 15
- 239000007800 oxidant agent Substances 0.000 claims description 9
- 239000003945 anionic surfactant Substances 0.000 claims description 7
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 239000002453 shampoo Substances 0.000 claims description 6
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical group OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims description 6
- 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 5
- -1 alkali metal salt Chemical class 0.000 claims description 5
- 229910052708 sodium Inorganic materials 0.000 claims description 5
- 239000011734 sodium Substances 0.000 claims description 5
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 claims description 4
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 claims description 4
- 229940063953 ammonium lauryl sulfate Drugs 0.000 claims description 4
- 239000004094 surface-active agent Substances 0.000 claims description 4
- 230000001143 conditioned effect Effects 0.000 claims description 3
- 229910052783 alkali metal Inorganic materials 0.000 claims description 2
- 235000019396 potassium bromate Nutrition 0.000 claims description 2
- XWNSFEAWWGGSKJ-UHFFFAOYSA-N 4-acetyl-4-methylheptanedinitrile Chemical compound N#CCCC(C)(C(=O)C)CCC#N XWNSFEAWWGGSKJ-UHFFFAOYSA-N 0.000 claims 1
- 239000004153 Potassium bromate Substances 0.000 claims 1
- 229940094037 potassium bromate Drugs 0.000 claims 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical group [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 claims 1
- 239000006210 lotion Substances 0.000 description 46
- 239000000047 product Substances 0.000 description 19
- 229940124024 weight reducing agent Drugs 0.000 description 12
- 239000002280 amphoteric surfactant Substances 0.000 description 11
- 239000003599 detergent Substances 0.000 description 11
- 229920000642 polymer Polymers 0.000 description 11
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 8
- 230000003750 conditioning effect Effects 0.000 description 6
- 229920001577 copolymer Polymers 0.000 description 6
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 5
- 229920006395 saturated elastomer Polymers 0.000 description 5
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 4
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 4
- 150000001875 compounds Chemical class 0.000 description 4
- 239000003205 fragrance Substances 0.000 description 4
- 238000006386 neutralization reaction Methods 0.000 description 4
- 239000000243 solution Substances 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 3
- 125000004432 carbon atom Chemical group C* 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000000470 constituent Substances 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 2
- HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 2
- PQUCIEFHOVEZAU-UHFFFAOYSA-N Diammonium sulfite Chemical class [NH4+].[NH4+].[O-]S([O-])=O PQUCIEFHOVEZAU-UHFFFAOYSA-N 0.000 description 2
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 2
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 2
- 239000001361 adipic acid Substances 0.000 description 2
- 235000011037 adipic acid Nutrition 0.000 description 2
- 239000012670 alkaline solution Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 2
- 239000008365 aqueous carrier Substances 0.000 description 2
- 230000003766 combability Effects 0.000 description 2
- 239000013065 commercial product Substances 0.000 description 2
- 229960002433 cysteine Drugs 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-N dimethylselenoniopropionate Natural products CCC(O)=O XBDQKXXYIPTUBI-UHFFFAOYSA-N 0.000 description 2
- 238000004043 dyeing Methods 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 230000002045 lasting effect Effects 0.000 description 2
- 239000002244 precipitate Substances 0.000 description 2
- 125000001453 quaternary ammonium group Chemical group 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 2
- UZNHKBFIBYXPDV-UHFFFAOYSA-N trimethyl-[3-(2-methylprop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].CC(=C)C(=O)NCCC[N+](C)(C)C UZNHKBFIBYXPDV-UHFFFAOYSA-N 0.000 description 2
- GETQZCLCWQTVFV-UHFFFAOYSA-N trimethylamine Chemical compound CN(C)C GETQZCLCWQTVFV-UHFFFAOYSA-N 0.000 description 2
- 239000002888 zwitterionic surfactant Substances 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 1
- JKNCOURZONDCGV-UHFFFAOYSA-N 2-(dimethylamino)ethyl 2-methylprop-2-enoate Chemical compound CN(C)CCOC(=O)C(C)=C JKNCOURZONDCGV-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- XOJNSTWDNBJKRK-UHFFFAOYSA-N 2-aminoethyl prop-2-enoate;phosphoric acid Chemical compound OP(O)(O)=O.NCCOC(=O)C=C XOJNSTWDNBJKRK-UHFFFAOYSA-N 0.000 description 1
- QTDIEDOANJISNP-UHFFFAOYSA-N 2-dodecoxyethyl hydrogen sulfate Chemical compound CCCCCCCCCCCCOCCOS(O)(=O)=O QTDIEDOANJISNP-UHFFFAOYSA-N 0.000 description 1
- MZNSQRLUUXWLSB-UHFFFAOYSA-N 2-ethenyl-1h-pyrrole Chemical compound C=CC1=CC=CN1 MZNSQRLUUXWLSB-UHFFFAOYSA-N 0.000 description 1
- KGIGUEBEKRSTEW-UHFFFAOYSA-N 2-vinylpyridine Chemical compound C=CC1=CC=CC=N1 KGIGUEBEKRSTEW-UHFFFAOYSA-N 0.000 description 1
- XYYUAOIALFMRGY-UHFFFAOYSA-N 3-[2-carboxyethyl(dodecyl)amino]propanoic acid Chemical compound CCCCCCCCCCCCN(CCC(O)=O)CCC(O)=O XYYUAOIALFMRGY-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 description 1
- 241001340526 Chrysoclista linneella Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 102000008186 Collagen Human genes 0.000 description 1
- 108010035532 Collagen Proteins 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- BRLQWZUYTZBJKN-UHFFFAOYSA-N Epichlorohydrin Chemical compound ClCC1CO1 BRLQWZUYTZBJKN-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 1
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 description 1
- 239000004141 Sodium laurylsulphate Substances 0.000 description 1
- 229920002472 Starch Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 239000012190 activator Substances 0.000 description 1
- ZZTCCAPMZLDHFM-UHFFFAOYSA-N ammonium thioglycolate Chemical compound [NH4+].[O-]C(=O)CS ZZTCCAPMZLDHFM-UHFFFAOYSA-N 0.000 description 1
- 229940075861 ammonium thioglycolate Drugs 0.000 description 1
- 101150010487 are gene Proteins 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 description 1
- 229910052794 bromium Inorganic materials 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 125000002091 cationic group Chemical group 0.000 description 1
- 239000003093 cationic surfactant Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 239000008406 cosmetic ingredient Substances 0.000 description 1
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 1
- 235000018417 cysteine Nutrition 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- XXJPSODUGQZOHA-UHFFFAOYSA-N diethyl sulfate;2-(dimethylamino)ethyl 2-methylprop-2-enoate;1-ethenylpyrrolidin-2-one Chemical compound C=CN1CCCC1=O.CCOS(=O)(=O)OCC.CN(C)CCOC(=O)C(C)=C XXJPSODUGQZOHA-UHFFFAOYSA-N 0.000 description 1
- 238000007865 diluting Methods 0.000 description 1
- VAYGXNSJCAHWJZ-UHFFFAOYSA-N dimethyl sulfate Chemical compound COS(=O)(=O)OC VAYGXNSJCAHWJZ-UHFFFAOYSA-N 0.000 description 1
- YIOJGTBNHQAVBO-UHFFFAOYSA-N dimethyl-bis(prop-2-enyl)azanium Chemical compound C=CC[N+](C)(C)CC=C YIOJGTBNHQAVBO-UHFFFAOYSA-N 0.000 description 1
- 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 1
- XFOSBZOUUACCCN-UHFFFAOYSA-M dimethyl-bis(prop-2-enyl)azanium;prop-2-enamide;chloride Chemical compound [Cl-].NC(=O)C=C.C=CC[N+](C)(C)CC=C XFOSBZOUUACCCN-UHFFFAOYSA-M 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- JZKFHQMONDVVNF-UHFFFAOYSA-N dodecyl sulfate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCOS(O)(=O)=O JZKFHQMONDVVNF-UHFFFAOYSA-N 0.000 description 1
- JRBPAEWTRLWTQC-UHFFFAOYSA-N dodecylamine Chemical compound CCCCCCCCCCCCN JRBPAEWTRLWTQC-UHFFFAOYSA-N 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- PCIBVZXUNDZWRL-UHFFFAOYSA-N ethylene glycol monophosphate Chemical compound OCCOP(O)(O)=O PCIBVZXUNDZWRL-UHFFFAOYSA-N 0.000 description 1
- 125000005313 fatty acid group Chemical group 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 1
- 229920000831 ionic polymer Polymers 0.000 description 1
- 235000000396 iron Nutrition 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 150000004668 long chain fatty acids Chemical group 0.000 description 1
- 239000002480 mineral oil Substances 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- 125000001421 myristyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- 150000003003 phosphines Chemical class 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- OCATYIAKPYKMPG-UHFFFAOYSA-M potassium bromate Chemical class [K+].[O-]Br(=O)=O OCATYIAKPYKMPG-UHFFFAOYSA-M 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- 235000019260 propionic acid Nutrition 0.000 description 1
- IUVKMZGDUIUOCP-BTNSXGMBSA-N quinbolone Chemical compound O([C@H]1CC[C@H]2[C@H]3[C@@H]([C@]4(C=CC(=O)C=C4CC3)C)CC[C@@]21C)C1=CCCC1 IUVKMZGDUIUOCP-BTNSXGMBSA-N 0.000 description 1
- NXLOLUFNDSBYTP-UHFFFAOYSA-N retene Chemical compound C1=CC=C2C3=CC=C(C(C)C)C=C3C=CC2=C1C NXLOLUFNDSBYTP-UHFFFAOYSA-N 0.000 description 1
- 230000002441 reversible effect Effects 0.000 description 1
- 229920006298 saran Polymers 0.000 description 1
- XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- RYYKJJJTJZKILX-UHFFFAOYSA-M sodium octadecanoate Chemical compound [Na+].CCCCCCCCCCCCCCCCCC([O-])=O RYYKJJJTJZKILX-UHFFFAOYSA-M 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000008399 tap water Substances 0.000 description 1
- 235000020679 tap water Nutrition 0.000 description 1
- 238000010998 test method Methods 0.000 description 1
- 239000013585 weight reducing agent Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/04—Preparations for permanent waving or straightening the hair
-
- 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/22—Peroxides; Oxygen; Ozone
-
- 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
- A61K8/8141—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 only one carboxyl radical, or of salts, anhydrides, esters, amides, imides or nitriles thereof; Compositions of derivatives of such polymers
- A61K8/8158—Homopolymers or copolymers of amides or imides, e.g. (meth) acrylamide; Compositions of derivatives of such polymers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/81—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- 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)
-
- 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
-
- 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
- A61K2800/54—Polymers characterized by specific structures/properties
- A61K2800/542—Polymers characterized by specific structures/properties characterized by the charge
- A61K2800/5426—Polymers characterized by specific structures/properties characterized by the charge cationic
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)
- Emergency Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US34668482A | 1982-02-08 | 1982-02-08 |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| SE8300626D0 SE8300626D0 (sv) | 1983-02-07 |
| SE8300626L SE8300626L (sv) | 1983-08-09 |
| SE461436B true SE461436B (sv) | 1990-02-19 |
Family
ID=23360566
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| SE8300626A SE461436B (sv) | 1982-02-08 | 1983-02-07 | Foerfarande foer lockpermanentning eller rakpermanentning av haar jaemte permanentningskomposition foer anvaendning vid naemnda foerfarande |
Country Status (18)
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AU578780B2 (en) * | 1985-02-04 | 1988-11-03 | Chesebrough-Pond's Inc. | Hair waving and straightening compositions of matter |
| CA1266829A (en) * | 1985-02-07 | 1990-03-20 | Du Yung Hsiung | Permanent wave neutralizer composition and method |
| US4656043A (en) * | 1985-09-13 | 1987-04-07 | Richardson-Vicks Inc. | Peroxide-containing conditioning shampoo |
| JP2568083B2 (ja) * | 1987-05-18 | 1996-12-25 | 政夫 齋藤 | パ−マネント方法 |
| BR8905998A (pt) * | 1988-02-19 | 1990-05-08 | Amethyst Investment Group Inc | Processo para ondulamento do cabelo |
| US4996997A (en) * | 1988-02-19 | 1991-03-05 | Amethyst Investment Group, Inc. | Permanent waving process and compositions |
| FR2657254B1 (fr) * | 1990-01-19 | 1992-04-10 | Oreal | Composition cosmetique reductrice pour la permanente des cheveux, a base de n-acetylcysteamine et d'un polymere cationique, et son utilisation dans un procede de deformation permanente des cheveux. |
| JPH0624946A (ja) * | 1989-12-08 | 1994-02-01 | L'oreal Sa | 還元性化粧料組成物 |
| FR2655541B1 (fr) * | 1989-12-08 | 1992-02-21 | Oreal | Composition cosmetique reductrice pour la permanente des cheveux, a base de cysteamine et d'un polymere cationique, et son utilisation dans un procede de deformation permanente des cheveux. |
| US5415856A (en) * | 1990-05-08 | 1995-05-16 | Preemptive Advertising Inc. | Hair treatment compositions containing disaccharides |
| JP2516284B2 (ja) * | 1991-04-04 | 1996-07-24 | 花王株式会社 | ２剤式毛髪処理剤組成物及び毛髪処理方法 |
| FR2675379A1 (fr) * | 1991-04-16 | 1992-10-23 | Oreal | Composition capillaire de mise en forme des cheveux et procede de mise en forme correspondant. |
| JP2523418B2 (ja) * | 1991-08-13 | 1996-08-07 | 花王株式会社 | ２剤式ケラチン質繊維処理剤組成物 |
| GB2312444A (en) * | 1996-04-27 | 1997-10-29 | R & C Products Pty Ltd | Keratin fibre modification using quaternary ammonium compounds |
| US6125856A (en) * | 1999-04-21 | 2000-10-03 | Phild Co., Ltd. | Hair repair, styling, and straightening process |
| US6805136B2 (en) | 2001-11-02 | 2004-10-19 | Kenra, Llc | Hair relaxer |
| US6723308B2 (en) | 2001-11-02 | 2004-04-20 | Kenra, Llc | Hair clarifying treatment |
| DE10338883A1 (de) | 2003-08-23 | 2005-03-24 | Hans Schwarzkopf & Henkel Gmbh & Co. Kg | Verfahren zur Glättung keratinhaltiger Fasern |
| FR2997848B1 (fr) * | 2012-11-09 | 2015-01-16 | Oreal | Composition comprenant un derive dicarbonyle et procede de lissage des cheveux a partir de cette composition |
| EP4119122A1 (en) * | 2021-07-13 | 2023-01-18 | Kao Germany GmbH | Process for permanent waving keratin fibers |
| PL441751A1 (pl) * | 2022-07-17 | 2024-01-22 | Uniwersytet Jagielloński | Nowe kationowe polimery o selektywnych właściwościach przeciwgrzybicznych |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2980657A (en) * | 1954-07-06 | 1961-04-18 | Rohm & Haas | Quaternary ammonium compounds of polymers of acrylamido type and methods for making them |
| FR2010319A1 (enrdf_load_html_response) * | 1968-06-07 | 1970-02-13 | Roehm & Haas Gmbh | |
| US3912808A (en) * | 1970-02-25 | 1975-10-14 | Gillette Co | Hair waving and straightening process and composition containing water-soluble amino and quaternary ammonium polymers |
| US3986825A (en) * | 1972-06-29 | 1976-10-19 | The Gillette Company | Hair coloring composition containing water-soluble amino and quaternary ammonium polymers |
| US4027008A (en) * | 1975-05-14 | 1977-05-31 | The Gillette Company | Hair bleaching composition containing water-soluble amino and quaternary ammonium polymers |
| JPS5261237A (en) * | 1975-11-13 | 1977-05-20 | Oreal | New cosmetic compound on basis of quaternarized polymer |
| LU76955A1 (enrdf_load_html_response) * | 1977-03-15 | 1978-10-18 | ||
| US4366827A (en) * | 1979-12-28 | 1983-01-04 | Societe Anonyme Dite: L'oreal | Procedure for the permanent reshaping of hair, and composition intended for carrying out said procedure |
| FR2472382A1 (fr) * | 1979-12-28 | 1981-07-03 | Oreal | Procede de deformation permanente des cheveux |
| CA1138341A (en) * | 1980-01-23 | 1982-12-28 | Leszek J. Wolfram | Waving composition from a reducing agent and cationic polymer |
-
1983
- 1983-01-26 CA CA000420294A patent/CA1190857A/en not_active Expired
- 1983-01-26 NZ NZ203095A patent/NZ203095A/en unknown
- 1983-01-27 ES ES519303A patent/ES8501971A1/es not_active Expired
- 1983-01-28 MX MX196086A patent/MX158289A/es unknown
- 1983-02-02 DE DE19833303346 patent/DE3303346A1/de not_active Withdrawn
- 1983-02-03 NL NL8300412A patent/NL8300412A/nl not_active Application Discontinuation
- 1983-02-04 FR FR8301781A patent/FR2521004B1/fr not_active Expired
- 1983-02-04 GR GR70409A patent/GR77409B/el unknown
- 1983-02-07 SE SE8300626A patent/SE461436B/sv not_active IP Right Cessation
- 1983-02-07 CH CH684/83A patent/CH660114A5/de not_active IP Right Cessation
- 1983-02-07 IE IE238/83A patent/IE53928B1/en not_active IP Right Cessation
- 1983-02-07 IT IT47676/83A patent/IT1203648B/it active
- 1983-02-07 GB GB08303349A patent/GB2114616B/en not_active Expired
- 1983-02-07 BR BR8300583A patent/BR8300583A/pt unknown
- 1983-02-08 JP JP58018240A patent/JPS58150506A/ja active Granted
- 1983-02-08 ZA ZA83863A patent/ZA83863B/xx unknown
- 1983-02-08 DK DK51883A patent/DK51883A/da not_active Application Discontinuation
- 1983-02-08 BE BE0/210079A patent/BE895854A/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| FR2521004A1 (fr) | 1983-08-12 |
| IT1203648B (it) | 1989-02-15 |
| NZ203095A (en) | 1986-10-08 |
| NL8300412A (nl) | 1983-09-01 |
| DE3303346A1 (de) | 1983-10-13 |
| IE830238L (en) | 1983-08-08 |
| ES519303A0 (es) | 1984-12-16 |
| IE53928B1 (en) | 1989-04-12 |
| BR8300583A (pt) | 1983-11-08 |
| CA1190857A (en) | 1985-07-23 |
| DK51883D0 (da) | 1983-02-08 |
| SE8300626D0 (sv) | 1983-02-07 |
| JPS58150506A (ja) | 1983-09-07 |
| JPH0425251B2 (enrdf_load_html_response) | 1992-04-30 |
| DK51883A (da) | 1983-08-09 |
| GR77409B (enrdf_load_html_response) | 1984-09-13 |
| MX158289A (es) | 1989-01-20 |
| BE895854A (fr) | 1983-08-08 |
| IT8347676A0 (it) | 1983-02-07 |
| GB2114616B (en) | 1985-12-18 |
| FR2521004B1 (fr) | 1987-01-23 |
| ES8501971A1 (es) | 1984-12-16 |
| AU1091683A (en) | 1983-08-18 |
| SE8300626L (sv) | 1983-08-09 |
| AU547971B2 (en) | 1985-11-14 |
| GB2114616A (en) | 1983-08-24 |
| ZA83863B (en) | 1983-11-30 |
| CH660114A5 (de) | 1987-03-31 |
| GB8303349D0 (en) | 1983-03-09 |
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