CA2587768A1 - Thickened hair colourant and bleaching compositions - Google Patents
Thickened hair colourant and bleaching compositions Download PDFInfo
- Publication number
- CA2587768A1 CA2587768A1 CA002587768A CA2587768A CA2587768A1 CA 2587768 A1 CA2587768 A1 CA 2587768A1 CA 002587768 A CA002587768 A CA 002587768A CA 2587768 A CA2587768 A CA 2587768A CA 2587768 A1 CA2587768 A1 CA 2587768A1
- Authority
- CA
- Canada
- Prior art keywords
- hair
- ions
- source
- hlb
- mixtures
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 216
- 210000004209 hair Anatomy 0.000 title claims abstract description 136
- 238000004061 bleaching Methods 0.000 title claims abstract description 53
- 238000004040 coloring Methods 0.000 claims abstract description 56
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims abstract description 44
- 239000007800 oxidant agent Substances 0.000 claims abstract description 39
- 239000002562 thickening agent Substances 0.000 claims abstract description 28
- 239000002516 radical scavenger Substances 0.000 claims abstract description 26
- -1 ammonium ions Chemical class 0.000 claims description 115
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 claims description 37
- 239000004094 surface-active agent Substances 0.000 claims description 37
- 125000004432 carbon atom Chemical group C* 0.000 claims description 36
- 230000001590 oxidative effect Effects 0.000 claims description 36
- 238000000034 method Methods 0.000 claims description 27
- 229920003171 Poly (ethylene oxide) Polymers 0.000 claims description 25
- 125000000217 alkyl group Chemical group 0.000 claims description 24
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical group C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 claims description 22
- 238000002156 mixing Methods 0.000 claims description 21
- 239000002736 nonionic surfactant Substances 0.000 claims description 20
- 239000002243 precursor Substances 0.000 claims description 20
- 150000002500 ions Chemical class 0.000 claims description 19
- 229910019142 PO4 Inorganic materials 0.000 claims description 18
- 235000021317 phosphate Nutrition 0.000 claims description 18
- 150000003839 salts Chemical group 0.000 claims description 15
- 238000002844 melting Methods 0.000 claims description 14
- 230000008018 melting Effects 0.000 claims description 14
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 13
- 229910052757 nitrogen Inorganic materials 0.000 claims description 13
- 238000011282 treatment Methods 0.000 claims description 12
- 150000002191 fatty alcohols Chemical class 0.000 claims description 11
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 claims description 9
- 239000003945 anionic surfactant Substances 0.000 claims description 9
- 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
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerol Natural products OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims description 7
- 239000003093 cationic surfactant Substances 0.000 claims description 7
- 239000010452 phosphate Substances 0.000 claims description 7
- 125000002877 alkyl aryl group Chemical group 0.000 claims description 6
- 150000005215 alkyl ethers Chemical class 0.000 claims description 6
- 125000000129 anionic group Chemical group 0.000 claims description 6
- 150000002148 esters Chemical class 0.000 claims description 6
- 229910052760 oxygen Inorganic materials 0.000 claims description 6
- 239000001301 oxygen Substances 0.000 claims description 6
- 150000003467 sulfuric acid derivatives Chemical class 0.000 claims description 6
- 150000007942 carboxylates Chemical class 0.000 claims description 5
- 239000001257 hydrogen Substances 0.000 claims description 5
- 229910052739 hydrogen Inorganic materials 0.000 claims description 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 5
- 150000003013 phosphoric acid derivatives Chemical class 0.000 claims description 5
- 150000003242 quaternary ammonium salts Chemical class 0.000 claims description 5
- 125000001273 sulfonato group Chemical group [O-]S(*)(=O)=O 0.000 claims description 5
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 4
- 125000002252 acyl group Chemical group 0.000 claims description 4
- 125000003342 alkenyl group Chemical group 0.000 claims description 4
- 229910052799 carbon Inorganic materials 0.000 claims description 4
- 150000001768 cations Chemical class 0.000 claims description 4
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 4
- 125000004433 nitrogen atom Chemical group N* 0.000 claims description 4
- 230000037308 hair color Effects 0.000 claims description 3
- 239000002202 Polyethylene glycol Substances 0.000 claims description 2
- 150000002170 ethers Chemical class 0.000 claims description 2
- 229920001223 polyethylene glycol Polymers 0.000 claims description 2
- 239000011369 resultant mixture Substances 0.000 claims description 2
- 230000000717 retained effect Effects 0.000 claims description 2
- 230000000063 preceeding effect Effects 0.000 claims 1
- 238000004519 manufacturing process Methods 0.000 abstract description 5
- 230000006378 damage Effects 0.000 abstract description 4
- 239000000975 dye Substances 0.000 description 41
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 29
- 239000003795 chemical substances by application Substances 0.000 description 16
- 229910021529 ammonia Inorganic materials 0.000 description 15
- 230000008719 thickening Effects 0.000 description 15
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 15
- 125000001424 substituent group Chemical group 0.000 description 13
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 12
- 238000004043 dyeing Methods 0.000 description 12
- 239000000118 hair dye Substances 0.000 description 12
- 125000005842 heteroatom Chemical group 0.000 description 12
- 239000001099 ammonium carbonate Substances 0.000 description 11
- 239000006210 lotion Substances 0.000 description 11
- 230000008569 process Effects 0.000 description 11
- 239000007787 solid Substances 0.000 description 11
- 125000001931 aliphatic group Chemical group 0.000 description 9
- 150000001875 compounds Chemical class 0.000 description 9
- 230000003750 conditioning effect Effects 0.000 description 9
- 238000009472 formulation Methods 0.000 description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 9
- 229920000642 polymer Polymers 0.000 description 9
- 150000003254 radicals Chemical class 0.000 description 9
- 235000012501 ammonium carbonate Nutrition 0.000 description 8
- 239000000463 material Substances 0.000 description 8
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 8
- 239000003921 oil Substances 0.000 description 8
- 230000003113 alkalizing effect Effects 0.000 description 7
- 125000003118 aryl group Chemical group 0.000 description 7
- 230000000694 effects Effects 0.000 description 7
- BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 6
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 description 6
- 238000006243 chemical reaction Methods 0.000 description 6
- 125000004404 heteroalkyl group Chemical group 0.000 description 6
- 125000005010 perfluoroalkyl group Chemical group 0.000 description 6
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 description 5
- KXDHJXZQYSOELW-UHFFFAOYSA-N carbonic acid monoamide Natural products NC(O)=O KXDHJXZQYSOELW-UHFFFAOYSA-N 0.000 description 5
- 239000003086 colorant Substances 0.000 description 5
- 230000009977 dual effect Effects 0.000 description 5
- 125000000623 heterocyclic group Chemical group 0.000 description 5
- 239000007788 liquid Substances 0.000 description 5
- GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 description 5
- 230000008961 swelling Effects 0.000 description 5
- KFZMGEQAYNKOFK-UHFFFAOYSA-N 2-propanol Substances CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 description 4
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 4
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 4
- XUMBMVFBXHLACL-UHFFFAOYSA-N Melanin Chemical compound O=C1C(=O)C(C2=CNC3=C(C(C(=O)C4=C32)=O)C)=C2C4=CNC2=C1C XUMBMVFBXHLACL-UHFFFAOYSA-N 0.000 description 4
- UIIMBOGNXHQVGW-UHFFFAOYSA-M Sodium bicarbonate Chemical compound [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 4
- BVCZEBOGSOYJJT-UHFFFAOYSA-N ammonium carbamate Chemical compound [NH4+].NC([O-])=O BVCZEBOGSOYJJT-UHFFFAOYSA-N 0.000 description 4
- 150000003863 ammonium salts Chemical class 0.000 description 4
- 229920006317 cationic polymer Polymers 0.000 description 4
- 229960000541 cetyl alcohol Drugs 0.000 description 4
- 239000000835 fiber Substances 0.000 description 4
- 210000003128 head Anatomy 0.000 description 4
- 239000004615 ingredient Substances 0.000 description 4
- 125000002950 monocyclic group Chemical group 0.000 description 4
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 4
- 150000002978 peroxides Chemical class 0.000 description 4
- 125000003367 polycyclic group Polymers 0.000 description 4
- 229920001296 polysiloxane Polymers 0.000 description 4
- 229910052708 sodium Inorganic materials 0.000 description 4
- 239000011734 sodium Substances 0.000 description 4
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 229910052717 sulfur Inorganic materials 0.000 description 4
- VKZRWSNIWNFCIQ-WDSKDSINSA-N (2s)-2-[2-[[(1s)-1,2-dicarboxyethyl]amino]ethylamino]butanedioic acid Chemical compound OC(=O)C[C@@H](C(O)=O)NCCN[C@H](C(O)=O)CC(O)=O VKZRWSNIWNFCIQ-WDSKDSINSA-N 0.000 description 3
- CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 description 3
- 229910000013 Ammonium bicarbonate Inorganic materials 0.000 description 3
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 3
- 239000000443 aerosol Substances 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 3
- 239000007864 aqueous solution Substances 0.000 description 3
- 239000002585 base Substances 0.000 description 3
- 239000013522 chelant Substances 0.000 description 3
- 239000002537 cosmetic Substances 0.000 description 3
- 239000000982 direct dye Substances 0.000 description 3
- 239000000839 emulsion Substances 0.000 description 3
- 230000003700 hair damage Effects 0.000 description 3
- 210000004919 hair shaft Anatomy 0.000 description 3
- 229910052736 halogen Inorganic materials 0.000 description 3
- 150000002367 halogens Chemical class 0.000 description 3
- RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 description 3
- 239000000543 intermediate Substances 0.000 description 3
- JXDYKVIHCLTXOP-UHFFFAOYSA-N isatin Chemical compound C1=CC=C2C(=O)C(=O)NC2=C1 JXDYKVIHCLTXOP-UHFFFAOYSA-N 0.000 description 3
- 230000007246 mechanism Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 230000004048 modification Effects 0.000 description 3
- 238000012986 modification Methods 0.000 description 3
- 229910052698 phosphorus Inorganic materials 0.000 description 3
- 239000011736 potassium bicarbonate Substances 0.000 description 3
- 229910000028 potassium bicarbonate Inorganic materials 0.000 description 3
- 235000015497 potassium bicarbonate Nutrition 0.000 description 3
- TYJJADVDDVDEDZ-UHFFFAOYSA-M potassium hydrogencarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 description 3
- 229940086066 potassium hydrogencarbonate Drugs 0.000 description 3
- 229910052710 silicon Inorganic materials 0.000 description 3
- MWNQXXOSWHCCOZ-UHFFFAOYSA-L sodium;oxido carbonate Chemical class [Na+].[O-]OC([O-])=O MWNQXXOSWHCCOZ-UHFFFAOYSA-L 0.000 description 3
- 125000004417 unsaturated alkyl group Chemical group 0.000 description 3
- 238000005406 washing Methods 0.000 description 3
- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- WPGVTIIXIAJUQK-UHFFFAOYSA-N 2-(2-hexadecoxyethoxy)ethyl dihydrogen phosphate Chemical compound CCCCCCCCCCCCCCCCOCCOCCOP(O)(O)=O WPGVTIIXIAJUQK-UHFFFAOYSA-N 0.000 description 2
- ILCOCZBHMDEIAI-UHFFFAOYSA-N 2-(2-octadecoxyethoxy)ethanol Chemical compound CCCCCCCCCCCCCCCCCCOCCOCCO ILCOCZBHMDEIAI-UHFFFAOYSA-N 0.000 description 2
- PMNLUUOXGOOLSP-UHFFFAOYSA-N 2-mercaptopropanoic acid Chemical compound CC(S)C(O)=O PMNLUUOXGOOLSP-UHFFFAOYSA-N 0.000 description 2
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- HWWIVWKTKZAORO-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-ol Chemical compound O1CCNC2=CC(O)=CC=C21 HWWIVWKTKZAORO-UHFFFAOYSA-N 0.000 description 2
- NZDXSXLYLMHYJA-UHFFFAOYSA-M 4-[(1,3-dimethylimidazol-1-ium-2-yl)diazenyl]-n,n-dimethylaniline;chloride Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1N=NC1=[N+](C)C=CN1C NZDXSXLYLMHYJA-UHFFFAOYSA-M 0.000 description 2
- JQVAPEJNIZULEK-UHFFFAOYSA-N 4-chlorobenzene-1,3-diol Chemical compound OC1=CC=C(Cl)C(O)=C1 JQVAPEJNIZULEK-UHFFFAOYSA-N 0.000 description 2
- SGNZYJXNUURYCH-UHFFFAOYSA-N 5,6-dihydroxyindole Chemical compound C1=C(O)C(O)=CC2=C1NC=C2 SGNZYJXNUURYCH-UHFFFAOYSA-N 0.000 description 2
- NLXLAEXVIDQMFP-UHFFFAOYSA-N Ammonia chloride Chemical compound [NH4+].[Cl-] NLXLAEXVIDQMFP-UHFFFAOYSA-N 0.000 description 2
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 2
- 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 2
- 102000011782 Keratins Human genes 0.000 description 2
- 108010076876 Keratins Proteins 0.000 description 2
- YNAVUWVOSKDBBP-UHFFFAOYSA-N Morpholine Chemical compound C1COCCN1 YNAVUWVOSKDBBP-UHFFFAOYSA-N 0.000 description 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical compound C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical group CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 2
- KYQCOXFCLRTKLS-UHFFFAOYSA-N Pyrazine Chemical compound C1=CN=CC=N1 KYQCOXFCLRTKLS-UHFFFAOYSA-N 0.000 description 2
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 2
- 239000005864 Sulphur Substances 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 125000003545 alkoxy group Chemical group 0.000 description 2
- 150000001450 anions Chemical class 0.000 description 2
- 235000010323 ascorbic acid Nutrition 0.000 description 2
- 229960005070 ascorbic acid Drugs 0.000 description 2
- 239000011668 ascorbic acid Substances 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- YSJGOMATDFSEED-UHFFFAOYSA-M behentrimonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C YSJGOMATDFSEED-UHFFFAOYSA-M 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- WGQKYBSKWIADBV-UHFFFAOYSA-N benzylamine Chemical compound NCC1=CC=CC=C1 WGQKYBSKWIADBV-UHFFFAOYSA-N 0.000 description 2
- 229910052794 bromium Inorganic materials 0.000 description 2
- 150000005323 carbonate salts Chemical class 0.000 description 2
- 239000004359 castor oil Substances 0.000 description 2
- 235000019438 castor oil Nutrition 0.000 description 2
- 229910052801 chlorine Inorganic materials 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
- 210000001520 comb Anatomy 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- 239000006071 cream Substances 0.000 description 2
- 230000007812 deficiency Effects 0.000 description 2
- 238000005516 engineering process Methods 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- 150000002193 fatty amides Chemical class 0.000 description 2
- 235000011187 glycerol Nutrition 0.000 description 2
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 2
- UYTPUPDQBNUYGX-UHFFFAOYSA-N guanine Chemical compound O=C1NC(N)=NC2=C1N=CN2 UYTPUPDQBNUYGX-UHFFFAOYSA-N 0.000 description 2
- 229960004592 isopropanol Drugs 0.000 description 2
- 239000002480 mineral oil Substances 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 2
- 229920000137 polyphosphoric acid Polymers 0.000 description 2
- 229960003975 potassium Drugs 0.000 description 2
- 229910052700 potassium Inorganic materials 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 description 2
- 230000005588 protonation Effects 0.000 description 2
- 229910000030 sodium bicarbonate Inorganic materials 0.000 description 2
- 235000017557 sodium bicarbonate Nutrition 0.000 description 2
- JQWHASGSAFIOCM-UHFFFAOYSA-M sodium periodate Chemical compound [Na+].[O-]I(=O)(=O)=O JQWHASGSAFIOCM-UHFFFAOYSA-M 0.000 description 2
- 235000010265 sodium sulphite Nutrition 0.000 description 2
- 239000000243 solution Substances 0.000 description 2
- 239000003381 stabilizer Substances 0.000 description 2
- 230000003068 static effect Effects 0.000 description 2
- 229940098760 steareth-2 Drugs 0.000 description 2
- 229910021653 sulphate ion Inorganic materials 0.000 description 2
- YXFVVABEGXRONW-UHFFFAOYSA-N toluene Substances CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 2
- 238000006276 transfer reaction Methods 0.000 description 2
- DJUGBKWOBAOTFA-UHFFFAOYSA-N (2,5,6-triaminopyrimidin-4-yl) hydrogen sulfate Chemical compound NC1=NC(N)=C(N)C(OS(O)(=O)=O)=N1 DJUGBKWOBAOTFA-UHFFFAOYSA-N 0.000 description 1
- WVOAPRDRMLHUMI-UHFFFAOYSA-N (2-methylnaphthalen-1-yl) acetate Chemical compound C1=CC=C2C(OC(=O)C)=C(C)C=CC2=C1 WVOAPRDRMLHUMI-UHFFFAOYSA-N 0.000 description 1
- JNYAEWCLZODPBN-JGWLITMVSA-N (2r,3r,4s)-2-[(1r)-1,2-dihydroxyethyl]oxolane-3,4-diol Chemical class OC[C@@H](O)[C@H]1OC[C@H](O)[C@H]1O JNYAEWCLZODPBN-JGWLITMVSA-N 0.000 description 1
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- YQEMORVAKMFKLG-UHFFFAOYSA-N glycerine monostearate Natural products CCCCCCCCCCCCCCCCCC(=O)OC(CO)CO YQEMORVAKMFKLG-UHFFFAOYSA-N 0.000 description 1
- SVUQHVRAGMNPLW-UHFFFAOYSA-N glycerol monostearate Natural products CCCCCCCCCCCCCCCCC(=O)OCC(O)CO SVUQHVRAGMNPLW-UHFFFAOYSA-N 0.000 description 1
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- 150000002334 glycols Chemical class 0.000 description 1
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- 229940093915 gynecological organic acid Drugs 0.000 description 1
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- XMBWDFGMSWQBCA-UHFFFAOYSA-N hydrogen iodide Chemical compound I XMBWDFGMSWQBCA-UHFFFAOYSA-N 0.000 description 1
- KDNFLUWYIMPBSA-UHFFFAOYSA-N hydrogen peroxide;1,3,5-triazine-2,4,6-triamine Chemical compound OO.NC1=NC(N)=NC(N)=N1 KDNFLUWYIMPBSA-UHFFFAOYSA-N 0.000 description 1
- ZNTBVZRXCXYINT-UHFFFAOYSA-N hydrogen sulfate;1h-pyrazol-1-ium Chemical compound C=1C=NNC=1.OS(O)(=O)=O ZNTBVZRXCXYINT-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 230000006872 improvement Effects 0.000 description 1
- 238000011065 in-situ storage Methods 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- 239000002563 ionic surfactant Substances 0.000 description 1
- 229940048848 lauryl glucoside Drugs 0.000 description 1
- VGSVNUGKHOVSPK-UHFFFAOYSA-N leukoaminochrome Chemical compound C1=C(O)C(O)=CC2=C1NCC2 VGSVNUGKHOVSPK-UHFFFAOYSA-N 0.000 description 1
- 239000012669 liquid formulation Substances 0.000 description 1
- 229910052744 lithium Inorganic materials 0.000 description 1
- XGZVUEUWXADBQD-UHFFFAOYSA-L lithium carbonate Chemical compound [Li+].[Li+].[O-]C([O-])=O XGZVUEUWXADBQD-UHFFFAOYSA-L 0.000 description 1
- 229910052808 lithium carbonate Inorganic materials 0.000 description 1
- 229940018564 m-phenylenediamine Drugs 0.000 description 1
- 239000011777 magnesium Substances 0.000 description 1
- 229910052749 magnesium Inorganic materials 0.000 description 1
- ZLNQQNXFFQJAID-UHFFFAOYSA-L magnesium carbonate Chemical compound [Mg+2].[O-]C([O-])=O ZLNQQNXFFQJAID-UHFFFAOYSA-L 0.000 description 1
- 239000001095 magnesium carbonate Substances 0.000 description 1
- 229910000021 magnesium carbonate Inorganic materials 0.000 description 1
- 159000000003 magnesium salts Chemical class 0.000 description 1
- KBOPZPXVLCULAV-UHFFFAOYSA-N mesalamine Chemical compound NC1=CC=C(O)C(C(O)=O)=C1 KBOPZPXVLCULAV-UHFFFAOYSA-N 0.000 description 1
- 229960004963 mesalazine Drugs 0.000 description 1
- 229910021645 metal ion Inorganic materials 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- JZMJDSHXVKJFKW-UHFFFAOYSA-M methyl sulfate(1-) Chemical compound COS([O-])(=O)=O JZMJDSHXVKJFKW-UHFFFAOYSA-M 0.000 description 1
- 231100001067 mild skin irritation Toxicity 0.000 description 1
- 235000010446 mineral oil Nutrition 0.000 description 1
- 239000003607 modifier Substances 0.000 description 1
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- 235000011929 mousse Nutrition 0.000 description 1
- KHPAAXRLVYMUHU-UHFFFAOYSA-N n-[2-(diethylamino)ethyl]docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)NCCN(CC)CC KHPAAXRLVYMUHU-UHFFFAOYSA-N 0.000 description 1
- MNAZHGAWPCLLGX-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]docosanamide Chemical compound CCCCCCCCCCCCCCCCCCCCCC(=O)NCCCN(C)C MNAZHGAWPCLLGX-UHFFFAOYSA-N 0.000 description 1
- HJXPIPGLPXVLGN-UHFFFAOYSA-N n-[3-(dimethylamino)propyl]icosanamide Chemical compound CCCCCCCCCCCCCCCCCCCC(=O)NCCCN(C)C HJXPIPGLPXVLGN-UHFFFAOYSA-N 0.000 description 1
- LLLILZLFKGJCCV-UHFFFAOYSA-M n-methyl-n-[(1-methylpyridin-1-ium-4-yl)methylideneamino]aniline;methyl sulfate Chemical compound COS([O-])(=O)=O.C=1C=CC=CC=1N(C)\N=C\C1=CC=[N+](C)C=C1 LLLILZLFKGJCCV-UHFFFAOYSA-M 0.000 description 1
- XWLUFINGMMDFPD-UHFFFAOYSA-N naphthalen-1-ol Chemical compound C1=CC=C2C(O)=CC=CC2=C1.C1=CC=C2C(O)=CC=CC2=C1 XWLUFINGMMDFPD-UHFFFAOYSA-N 0.000 description 1
- XPYORFZFOLPGSK-UHFFFAOYSA-N naphthalene-1,5-diol Chemical compound C1=CC=C2C(O)=CC=CC2=C1O.C1=CC=C2C(O)=CC=CC2=C1O XPYORFZFOLPGSK-UHFFFAOYSA-N 0.000 description 1
- FLKLRKFRNSOVMT-UHFFFAOYSA-N naphthalene-1,7-diol Chemical compound C1=CC=C(O)C2=CC(O)=CC=C21.C1=CC=C(O)C2=CC(O)=CC=C21 FLKLRKFRNSOVMT-UHFFFAOYSA-N 0.000 description 1
- DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-UHFFFAOYSA-N 0.000 description 1
- 150000002828 nitro derivatives Chemical class 0.000 description 1
- 238000005580 one pot reaction Methods 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 150000001451 organic peroxides Chemical class 0.000 description 1
- 239000003002 pH adjusting agent Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 239000001024 permanent hair color Substances 0.000 description 1
- 125000005342 perphosphate group Chemical group 0.000 description 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- PTMHPRAIXMAOOB-UHFFFAOYSA-N phosphoramidic acid Chemical class NP(O)(O)=O PTMHPRAIXMAOOB-UHFFFAOYSA-N 0.000 description 1
- 229920002553 poly(2-methacrylolyloxyethyltrimethylammonium chloride) polymer Polymers 0.000 description 1
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- 229920005862 polyol Polymers 0.000 description 1
- 229920001282 polysaccharide Polymers 0.000 description 1
- 239000005017 polysaccharide Substances 0.000 description 1
- 229910000027 potassium carbonate Inorganic materials 0.000 description 1
- 235000011181 potassium carbonates Nutrition 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical compound NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 239000006254 rheological additive Substances 0.000 description 1
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- 239000002453 shampoo Substances 0.000 description 1
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- 230000036556 skin irritation Effects 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 229910000029 sodium carbonate Inorganic materials 0.000 description 1
- 235000017550 sodium carbonate Nutrition 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
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- 125000004079 stearyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
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- 150000004685 tetrahydrates Chemical class 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 231100000583 toxicological profile Toxicity 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 238000002604 ultrasonography Methods 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/342—Alcohols having more than seven atoms in an unbroken chain
-
- 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
-
- 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
- A61K8/42—Amides
-
- 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
- A61K8/55—Phosphorus compounds
- A61K8/556—Derivatives containing from 2 to 10 oxyalkylene groups
-
- 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
- A61Q5/08—Preparations for bleaching the hair
-
- 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
- A61Q5/10—Preparations for permanently dyeing the hair
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 (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP04257509 | 2004-12-02 | ||
| EP04257509.2 | 2004-12-02 | ||
| PCT/US2005/043461 WO2006060568A1 (en) | 2004-12-02 | 2005-12-01 | Thickened hair colourant and bleaching compositions |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2587768A1 true CA2587768A1 (en) | 2006-06-08 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002587768A Abandoned CA2587768A1 (en) | 2004-12-02 | 2005-12-01 | Thickened hair colourant and bleaching compositions |
Country Status (8)
| Country | Link |
|---|---|
| US (1) | US7875269B2 (enExample) |
| JP (1) | JP5318418B2 (enExample) |
| CN (1) | CN101068599B (enExample) |
| AU (1) | AU2005311859B8 (enExample) |
| BR (1) | BRPI0518792A2 (enExample) |
| CA (1) | CA2587768A1 (enExample) |
| MX (1) | MX2007006404A (enExample) |
| WO (1) | WO2006060568A1 (enExample) |
Families Citing this family (31)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5179191B2 (ja) * | 2004-12-02 | 2013-04-10 | ザ プロクター アンド ギャンブル カンパニー | 高分子増粘毛髪染色及び漂白組成物 |
| JP2008521832A (ja) * | 2004-12-02 | 2008-06-26 | ザ プロクター アンド ギャンブル カンパニー | 高濃度カーボネート及び／又は酸化剤毛髪染色組成物 |
| EP1721598B1 (en) * | 2005-04-29 | 2011-09-28 | The Procter & Gamble Company | Micelle thickening systems for hair colourant and bleaching compositions |
| DE602006016590D1 (de) * | 2006-07-12 | 2010-10-14 | Procter & Gamble | Auf Gelnetzwerk-Emulgatoren basierende Verdickersysteme für Haarfärbe und Haaraufhellungszusammensetzungen |
| FR2929110B1 (fr) * | 2008-03-28 | 2010-04-16 | Oreal | Dispersion aqueuse oxydante pour le traitement des fibres keratiniques comprenant un compose amphiphile non ionique a caractere hydrophobe |
| JP5711883B2 (ja) * | 2008-12-19 | 2015-05-07 | ロレアル | 脂肪物質に富む水性組成物の存在下で、淡色化し、あるいは淡色化直接染色し、あるいは酸化染色する方法、及びそのためのデバイス |
| US8697305B2 (en) * | 2009-03-16 | 2014-04-15 | Kabushiki Kaisha Toyoda Jidoshokki | Fuel cell system |
| EP2308564B1 (en) * | 2009-09-18 | 2018-12-19 | Noxell Corporation | Thickened hair colourant and bleaching compositions |
| ES2555229T3 (es) * | 2009-09-18 | 2015-12-29 | The Procter & Gamble Company | Composiciones de colorante espesado y de blanqueador del cabello |
| ATE556694T1 (de) * | 2010-01-08 | 2012-05-15 | Procter & Gamble | Eingedickte haarfärbe- und - bleichzusammensetzungen |
| US8821591B2 (en) * | 2011-04-28 | 2014-09-02 | Kao Corporation | Hair decoration article and hair dyeing and bleaching method using same |
| JP5990032B2 (ja) * | 2011-04-28 | 2016-09-07 | 花王株式会社 | 毛髪化粧品及びそれを用いた毛髪の染毛又は脱色方法 |
| JP5990033B2 (ja) * | 2011-12-14 | 2016-09-07 | 花王株式会社 | 毛髪化粧品及びそれを用いた毛髪の染毛又は脱色方法 |
| CA2864909A1 (en) * | 2012-02-24 | 2013-08-29 | The Procter & Gamble Company | Hair colouring methods and compositions thereof |
| IN2014DN08996A (enExample) * | 2012-05-23 | 2015-05-22 | Procter & Gamble | |
| WO2014180698A2 (en) * | 2013-05-09 | 2014-11-13 | Unilever Plc | Hair colouring kit |
| JP6414594B2 (ja) | 2013-08-23 | 2018-10-31 | ノクセル・コーポレーション | 毛髪染色方法及びそのキット |
| WO2015026991A2 (en) | 2013-08-23 | 2015-02-26 | The Procter & Gamble Company | Hair colouring methods and kits thereof |
| EP2881144A3 (en) | 2013-08-23 | 2015-07-15 | The Procter and Gamble Company | Hair treatment methods and kits thereof |
| US9339666B2 (en) | 2013-08-23 | 2016-05-17 | The Procter & Gamble Company | Hair colouring methods and kits thereof |
| WO2015026994A1 (en) | 2013-08-23 | 2015-02-26 | The Procter & Gamble Company | Hair colouring methods and kits thereof |
| CN105491996A (zh) * | 2013-08-23 | 2016-04-13 | 宝洁公司 | 毛发着色方法 |
| CA2919016A1 (en) | 2013-08-27 | 2015-03-05 | The Procter & Gamble Company | Hair treatment method, kit, recipient, and use thereof |
| EP2859880B1 (en) * | 2013-10-14 | 2018-02-14 | Noxell Corporation | Hair treatment composition, kit and method thereof |
| WO2018053522A1 (en) | 2016-09-19 | 2018-03-22 | Hitchcock Agostino Elizabeth | Methods and kits for coloring hair |
| JP7187660B2 (ja) * | 2018-03-27 | 2022-12-12 | ラボラトワール バイオステティーク コスメティーク ゲーエムベーハー ウント カンパニー カーゲー | 毛髪着色クリームおよび特定の緊張性化合物を含む顕色剤組成物を含む２成分毛髪処理キット |
| EP3784207A1 (en) * | 2018-04-24 | 2021-03-03 | Revlon | A cosmetic hair dyeing and/or bleaching composition, method, use and kit thereof |
| US11185485B2 (en) * | 2019-05-31 | 2021-11-30 | L'oreal | Hair coloring compositions and methods of using the same |
| CN114555048A (zh) * | 2019-06-28 | 2022-05-27 | 莱雅公司 | 用于角蛋白纤维的氧化染色的美容组合物 |
| WO2020259214A1 (en) * | 2019-06-28 | 2020-12-30 | L'oreal | Composition for dyeing keratin fibres and use thereof |
| US20210236404A1 (en) * | 2020-01-31 | 2021-08-05 | L'oreal | Compositions and methods for hair |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2117760B1 (enExample) | 1970-12-15 | 1974-03-01 | Gallia Sa Eugene | |
| FR2421606A1 (fr) | 1978-04-06 | 1979-11-02 | Oreal | Procede de teinture de fibres keratiniques en deux temps |
| CA1111349A (en) * | 1978-10-12 | 1981-10-27 | Richard Demarco | Low ammonia bleach compositions |
| FR2486394A1 (fr) * | 1979-11-28 | 1982-01-15 | Oreal | Composition destinee au traitement des fibres keratiniques a base de polymeres amphoteres et de polymeres anioniques |
| JPS60155108A (ja) | 1983-12-23 | 1985-08-15 | Kao Corp | 染毛剤組成物 |
| USRE33786E (en) | 1986-03-19 | 1992-01-07 | Clairol, Inc. | Hair dyeing process and composition |
| US4776855A (en) | 1986-03-19 | 1988-10-11 | Clairol Inc. | Hair dyeing process and composition |
| JPH0759490B2 (ja) | 1987-01-12 | 1995-06-28 | サンスタ−株式会社 | 染毛剤 |
| JPH0794372B2 (ja) | 1987-12-22 | 1995-10-11 | ホーユー株式会社 | クリーム状染毛剤第１剤組成物 |
| JPH0764711B2 (ja) | 1989-11-30 | 1995-07-12 | サンスター株式会社 | ２剤形染毛剤 |
| JPH0825858B2 (ja) * | 1991-06-04 | 1996-03-13 | ホーユー株式会社 | 染毛剤組成物 |
| EP0532272A3 (en) * | 1991-09-12 | 1993-07-28 | Unilever Plc | Hair conditioning composition |
| JPH06271435A (ja) | 1993-03-19 | 1994-09-27 | Takara Belmont Co Ltd | 毛髪染色剤 |
| US5376146A (en) | 1993-08-26 | 1994-12-27 | Bristol-Myers Squibb Company | Two-part aqueous composition for coloring hair, which forms a gel on mixing of the two parts |
| JPH08157345A (ja) | 1994-11-29 | 1996-06-18 | Oda Seiyaku Kk | 毛髪脱色染色方法及び毛髪脱色染色用粘性液 |
| JPH092925A (ja) | 1995-06-16 | 1997-01-07 | Shiseido Co Ltd | ２剤混合式化粧料 |
| GB9526711D0 (en) * | 1995-12-29 | 1996-02-28 | Procter & Gamble | Hair colouring composition |
| DE19705875C1 (de) | 1997-02-15 | 1998-04-02 | Wella Ag | Mittel zum oxidativen Färben von Haaren |
| DE19723538C1 (de) | 1997-06-05 | 1998-09-17 | Wella Ag | Pastenförmiges Mittel zum Bleichen von Haaren |
| JPH11199454A (ja) | 1998-01-08 | 1999-07-27 | Yamahatsu Sangyo Kk | ２液式酸化染毛剤及び２液式脱色剤 |
| GB9924885D0 (en) | 1999-10-20 | 1999-12-22 | Procter & Gamble | Hair colouring compositions and methods |
| JP3420143B2 (ja) | 1999-12-02 | 2003-06-23 | 花王株式会社 | 毛髪処理剤 |
| DE19959320A1 (de) * | 1999-12-09 | 2001-06-13 | Henkel Kgaa | Neue Farbstoffkombination |
| JP3762177B2 (ja) | 2000-01-25 | 2006-04-05 | 花王株式会社 | 毛髪処理剤 |
| DE10020887A1 (de) * | 2000-04-28 | 2001-10-31 | Henkel Kgaa | Neue Verwendung von Zuckertensiden und Fettsäurepartialglyceriden |
| JP4095756B2 (ja) | 2000-05-19 | 2008-06-04 | ホーユー株式会社 | 染毛剤組成物 |
| JP5529359B2 (ja) | 2000-12-06 | 2014-06-25 | ホーユー株式会社 | 酸化染毛剤組成物 |
| JP2002187826A (ja) | 2000-12-20 | 2002-07-05 | Shiseido Co Ltd | 脱色剤 |
| JP5214079B2 (ja) | 2000-12-27 | 2013-06-19 | ホーユー株式会社 | 染毛剤組成物 |
| JP3748377B2 (ja) | 2000-12-28 | 2006-02-22 | 花王株式会社 | 染毛剤組成物 |
| WO2002074273A1 (en) | 2001-03-20 | 2002-09-26 | The Procter & Gamble Company | Oxidizing compositions comprising a chelant and a conditioning agent and methods of treating hair |
| WO2002078661A2 (en) | 2001-03-20 | 2002-10-10 | The Procter & Gamble Company | Oxidizing compositions comprising a phosphonic acid type chelant and a conditioning agent and methods of treating hair |
| US7056497B2 (en) * | 2001-03-30 | 2006-06-06 | The Procter & Gamble Company | Hair bleach product |
| FR2824735A1 (fr) | 2001-05-16 | 2002-11-22 | Oreal | Composition pulverulente pour la decoloration des fibres keratiniques humaines |
| JP2002363048A (ja) * | 2001-05-31 | 2002-12-18 | Nicca Chemical Co Ltd | ２剤式染毛・脱色剤組成物用第１剤、２剤式染毛・脱色剤組成物キット、及びそれを用いた毛髪処理方法 |
| DE10160814A1 (de) * | 2001-12-11 | 2003-06-18 | Henkel Kgaa | Neue Entwickler-Kuppler-Kombination mit 2,4-Dichlor-3-aminophenol |
| JP2003231617A (ja) * | 2002-02-07 | 2003-08-19 | Seiwa Kasei:Kk | 毛髪化粧料 |
| GB0212516D0 (en) * | 2002-05-31 | 2002-07-10 | Procter & Gamble | Compositions for treating hair comprising a phosphate ester compound and an oxidising agent |
| US20040019980A1 (en) * | 2002-08-02 | 2004-02-05 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | One step hair coloring compositions using salts |
| US6821302B2 (en) | 2002-11-01 | 2004-11-23 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Permanent coloring of hair using carbonate salts and bicarbonate salts and using percarbamic acid precursors |
| JP2004161707A (ja) * | 2002-11-15 | 2004-06-10 | Nicca Chemical Co Ltd | 酸化染毛剤 |
| US20040098814A1 (en) | 2002-11-27 | 2004-05-27 | Unilever Home & Personal Care Usa, Division Of Conopco, Inc. | Method and composition for the gradual permanent coloring of hair which employ carbonates |
| JP4119235B2 (ja) * | 2002-12-12 | 2008-07-16 | クローダジャパン株式会社 | 染毛剤組成物 |
| FR2848843B1 (fr) | 2002-12-20 | 2005-07-01 | Oreal | Composition anhydre pateuse pour la decoloration et la coloration simultanee des fibres keratiniques humaines. |
| JP2004269466A (ja) * | 2003-03-12 | 2004-09-30 | Seiwa Kasei:Kk | 酸化型染毛剤 |
| EP1484047A1 (en) * | 2003-06-02 | 2004-12-08 | The Procter & Gamble Company | Hair colouring compositions |
| EP1484048B1 (en) | 2003-06-02 | 2019-01-02 | Noxell Corporation | Hair colouring compositions |
| JP4116936B2 (ja) | 2003-07-03 | 2008-07-09 | 花王株式会社 | 酸化染毛剤又は脱色剤組成物 |
| JP2005194202A (ja) | 2003-12-26 | 2005-07-21 | Kao Corp | 二剤式毛髪化粧料 |
| JP5179191B2 (ja) * | 2004-12-02 | 2013-04-10 | ザ プロクター アンド ギャンブル カンパニー | 高分子増粘毛髪染色及び漂白組成物 |
-
2005
- 2005-12-01 AU AU2005311859A patent/AU2005311859B8/en not_active Expired - Fee Related
- 2005-12-01 JP JP2007544505A patent/JP5318418B2/ja not_active Expired - Fee Related
- 2005-12-01 US US11/292,129 patent/US7875269B2/en not_active Expired - Fee Related
- 2005-12-01 CN CN200580041298XA patent/CN101068599B/zh not_active Expired - Fee Related
- 2005-12-01 MX MX2007006404A patent/MX2007006404A/es not_active Application Discontinuation
- 2005-12-01 WO PCT/US2005/043461 patent/WO2006060568A1/en not_active Ceased
- 2005-12-01 BR BRPI0518792-3A patent/BRPI0518792A2/pt not_active Application Discontinuation
- 2005-12-01 CA CA002587768A patent/CA2587768A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0518792A2 (pt) | 2008-12-09 |
| AU2005311859B2 (en) | 2011-12-08 |
| AU2005311859A1 (en) | 2006-06-08 |
| AU2005311859B8 (en) | 2012-01-19 |
| JP5318418B2 (ja) | 2013-10-16 |
| JP2008521923A (ja) | 2008-06-26 |
| WO2006060568A1 (en) | 2006-06-08 |
| CN101068599A (zh) | 2007-11-07 |
| CN101068599B (zh) | 2012-04-04 |
| MX2007006404A (es) | 2007-06-22 |
| US7875269B2 (en) | 2011-01-25 |
| US20060117498A1 (en) | 2006-06-08 |
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| EEER | Examination request | ||
| FZDE | Dead |
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