GB2557383A - Hair treatments - Google Patents
Hair treatments Download PDFInfo
- Publication number
- GB2557383A GB2557383A GB1711291.3A GB201711291A GB2557383A GB 2557383 A GB2557383 A GB 2557383A GB 201711291 A GB201711291 A GB 201711291A GB 2557383 A GB2557383 A GB 2557383A
- Authority
- GB
- United Kingdom
- Prior art keywords
- composition
- hair
- sulfur containing
- urea
- containing nucleophile
- 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.)
- Granted
Links
- 238000011282 treatment Methods 0.000 title description 3
- 239000000203 mixture Substances 0.000 claims abstract description 170
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims abstract description 48
- 239000002243 precursor Substances 0.000 claims abstract description 43
- 239000007788 liquid Substances 0.000 claims abstract description 37
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims abstract description 34
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 34
- 239000011593 sulfur Substances 0.000 claims abstract description 34
- 239000012038 nucleophile Substances 0.000 claims abstract description 33
- NYYSPVRERVXMLJ-UHFFFAOYSA-N 4,4-difluorocyclohexan-1-one Chemical compound FC1(F)CCC(=O)CC1 NYYSPVRERVXMLJ-UHFFFAOYSA-N 0.000 claims abstract description 31
- 239000004202 carbamide Substances 0.000 claims abstract description 30
- 239000012188 paraffin wax Substances 0.000 claims abstract description 20
- 230000002209 hydrophobic effect Effects 0.000 claims abstract description 19
- 238000000034 method Methods 0.000 claims abstract description 18
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical group OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 claims abstract description 16
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 abstract description 14
- 239000002253 acid Substances 0.000 abstract description 4
- RYYXDZDBXNUPOG-UHFFFAOYSA-N 4,5,6,7-tetrahydro-1,3-benzothiazole-2,6-diamine;dihydrochloride Chemical compound Cl.Cl.C1C(N)CCC2=C1SC(N)=N2 RYYXDZDBXNUPOG-UHFFFAOYSA-N 0.000 abstract description 2
- PNKUSGQVOMIXLU-UHFFFAOYSA-N Formamidine Chemical compound NC=N PNKUSGQVOMIXLU-UHFFFAOYSA-N 0.000 abstract description 2
- 102000011782 Keratins Human genes 0.000 abstract description 2
- 108010076876 Keratins Proteins 0.000 abstract description 2
- 239000000835 fiber Substances 0.000 abstract description 2
- 229940057995 liquid paraffin Drugs 0.000 abstract description 2
- 230000001590 oxidative effect Effects 0.000 abstract description 2
- 239000002736 nonionic surfactant Substances 0.000 description 12
- 239000004094 surface-active agent Substances 0.000 description 12
- PEDCQBHIVMGVHV-UHFFFAOYSA-N glycerol group Chemical group OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 11
- 239000002562 thickening agent Substances 0.000 description 9
- 230000000052 comparative effect Effects 0.000 description 7
- 239000004615 ingredient Substances 0.000 description 7
- 150000001875 compounds Chemical class 0.000 description 6
- BXWNKGSJHAJOGX-UHFFFAOYSA-N hexadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 6
- GLDOVTGHNKAZLK-UHFFFAOYSA-N octadecan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCO GLDOVTGHNKAZLK-UHFFFAOYSA-N 0.000 description 6
- YGSDEFSMJLZEOE-UHFFFAOYSA-N salicylic acid Chemical compound OC(=O)C1=CC=CC=C1O YGSDEFSMJLZEOE-UHFFFAOYSA-N 0.000 description 6
- 239000003093 cationic surfactant Substances 0.000 description 5
- WOWHHFRSBJGXCM-UHFFFAOYSA-M cetyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(C)C WOWHHFRSBJGXCM-UHFFFAOYSA-M 0.000 description 5
- 239000002280 amphoteric surfactant Substances 0.000 description 4
- 239000003945 anionic surfactant Substances 0.000 description 4
- 239000000872 buffer Substances 0.000 description 4
- 235000011187 glycerol Nutrition 0.000 description 4
- 238000004806 packaging method and process Methods 0.000 description 4
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 4
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 4
- 229920000053 polysorbate 80 Polymers 0.000 description 4
- 229940068968 polysorbate 80 Drugs 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Chemical compound OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 3
- 125000000217 alkyl group Chemical group 0.000 description 3
- 229960000541 cetyl alcohol Drugs 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
- 230000003750 conditioning effect Effects 0.000 description 3
- 150000002191 fatty alcohols Chemical class 0.000 description 3
- 239000003205 fragrance Substances 0.000 description 3
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 3
- FJKROLUGYXJWQN-UHFFFAOYSA-N papa-hydroxy-benzoic acid Natural products OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 3
- 229960004889 salicylic acid Drugs 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- MPNXSZJPSVBLHP-UHFFFAOYSA-N 2-chloro-n-phenylpyridine-3-carboxamide Chemical compound ClC1=NC=CC=C1C(=O)NC1=CC=CC=C1 MPNXSZJPSVBLHP-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
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- 239000004354 Hydroxyethyl cellulose Substances 0.000 description 2
- 229920000663 Hydroxyethyl cellulose Polymers 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 2
- ISLGHAYMGURDSU-UHFFFAOYSA-N aminomethanesulfinic acid Chemical compound NCS(O)=O ISLGHAYMGURDSU-UHFFFAOYSA-N 0.000 description 2
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 125000000129 anionic group Chemical group 0.000 description 2
- YSJGOMATDFSEED-UHFFFAOYSA-M behentrimonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)C YSJGOMATDFSEED-UHFFFAOYSA-M 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- MRUAUOIMASANKQ-UHFFFAOYSA-O carboxymethyl-[3-(dodecanoylamino)propyl]-dimethylazanium Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC(O)=O MRUAUOIMASANKQ-UHFFFAOYSA-O 0.000 description 2
- 125000002091 cationic group Chemical group 0.000 description 2
- 229960002788 cetrimonium chloride Drugs 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- -1 colourants Substances 0.000 description 2
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 2
- 235000018417 cysteine Nutrition 0.000 description 2
- 239000000975 dye Substances 0.000 description 2
- 235000019447 hydroxyethyl cellulose Nutrition 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 150000007522 mineralic acids Chemical class 0.000 description 2
- 150000007524 organic acids Chemical class 0.000 description 2
- 239000007800 oxidant agent Substances 0.000 description 2
- 150000002978 peroxides Chemical class 0.000 description 2
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- QBYIENPQHBMVBV-HFEGYEGKSA-N (2R)-2-hydroxy-2-phenylacetic acid Chemical compound O[C@@H](C(O)=O)c1ccccc1.O[C@@H](C(O)=O)c1ccccc1 QBYIENPQHBMVBV-HFEGYEGKSA-N 0.000 description 1
- BJEPYKJPYRNKOW-REOHCLBHSA-N (S)-malic acid Chemical compound OC(=O)[C@@H](O)CC(O)=O BJEPYKJPYRNKOW-REOHCLBHSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- HVYJSOSGTDINLW-UHFFFAOYSA-N 2-[dimethyl(octadecyl)azaniumyl]acetate Chemical compound CCCCCCCCCCCCCCCCCC[N+](C)(C)CC([O-])=O HVYJSOSGTDINLW-UHFFFAOYSA-N 0.000 description 1
- SQXSZTQNKBBYPM-UHFFFAOYSA-N 2-[docosyl(dimethyl)azaniumyl]acetate Chemical compound CCCCCCCCCCCCCCCCCCCCCC[N+](C)(C)CC([O-])=O SQXSZTQNKBBYPM-UHFFFAOYSA-N 0.000 description 1
- TYIOVYZMKITKRO-UHFFFAOYSA-N 2-[hexadecyl(dimethyl)azaniumyl]acetate Chemical compound CCCCCCCCCCCCCCCC[N+](C)(C)CC([O-])=O TYIOVYZMKITKRO-UHFFFAOYSA-N 0.000 description 1
- 229940058020 2-amino-2-methyl-1-propanol Drugs 0.000 description 1
- OSCJHTSDLYVCQC-UHFFFAOYSA-N 2-ethylhexyl 4-[[4-[4-(tert-butylcarbamoyl)anilino]-6-[4-(2-ethylhexoxycarbonyl)anilino]-1,3,5-triazin-2-yl]amino]benzoate Chemical compound C1=CC(C(=O)OCC(CC)CCCC)=CC=C1NC1=NC(NC=2C=CC(=CC=2)C(=O)NC(C)(C)C)=NC(NC=2C=CC(=CC=2)C(=O)OCC(CC)CCCC)=N1 OSCJHTSDLYVCQC-UHFFFAOYSA-N 0.000 description 1
- IXOCGRPBILEGOX-UHFFFAOYSA-N 3-[3-(dodecanoylamino)propyl-dimethylazaniumyl]-2-hydroxypropane-1-sulfonate Chemical compound CCCCCCCCCCCC(=O)NCCC[N+](C)(C)CC(O)CS([O-])(=O)=O IXOCGRPBILEGOX-UHFFFAOYSA-N 0.000 description 1
- DDGPBVIAYDDWDH-UHFFFAOYSA-N 3-[dodecyl(dimethyl)azaniumyl]-2-hydroxypropane-1-sulfonate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC(O)CS([O-])(=O)=O DDGPBVIAYDDWDH-UHFFFAOYSA-N 0.000 description 1
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 1
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- FEWJPZIEWOKRBE-JCYAYHJZSA-N Dextrotartaric acid Chemical compound OC(=O)[C@H](O)[C@@H](O)C(O)=O FEWJPZIEWOKRBE-JCYAYHJZSA-N 0.000 description 1
- 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 1
- DBVJJBKOTRCVKF-UHFFFAOYSA-N Etidronic acid Chemical compound OP(=O)(O)C(O)(C)P(O)(O)=O DBVJJBKOTRCVKF-UHFFFAOYSA-N 0.000 description 1
- IAJILQKETJEXLJ-UHFFFAOYSA-N Galacturonsaeure Natural products O=CC(O)C(O)C(O)C(O)C(O)=O IAJILQKETJEXLJ-UHFFFAOYSA-N 0.000 description 1
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 1
- GRYLNZFGIOXLOG-UHFFFAOYSA-N Nitric acid Chemical compound O[N+]([O-])=O GRYLNZFGIOXLOG-UHFFFAOYSA-N 0.000 description 1
- IWYDHOAUDWTVEP-UHFFFAOYSA-N R-2-phenyl-2-hydroxyacetic acid Natural products OC(=O)C(O)C1=CC=CC=C1 IWYDHOAUDWTVEP-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
- VBIIFPGSPJYLRR-UHFFFAOYSA-M Stearyltrimethylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)C VBIIFPGSPJYLRR-UHFFFAOYSA-M 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 1
- GNVMUORYQLCPJZ-UHFFFAOYSA-M Thiocarbamate Chemical compound NC([S-])=O GNVMUORYQLCPJZ-UHFFFAOYSA-M 0.000 description 1
- 229960000583 acetic acid Drugs 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- IAJILQKETJEXLJ-QTBDOELSSA-N aldehydo-D-glucuronic acid Chemical compound O=C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)C(O)=O IAJILQKETJEXLJ-QTBDOELSSA-N 0.000 description 1
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 150000001340 alkali metals Chemical class 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 125000005210 alkyl ammonium group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-N alpha-hydroxysuccinic acid Natural products OC(=O)C(O)CC(O)=O BJEPYKJPYRNKOW-UHFFFAOYSA-N 0.000 description 1
- 229910000147 aluminium phosphate Inorganic materials 0.000 description 1
- 150000001412 amines Chemical class 0.000 description 1
- MDHRKTMFBQWLPG-UHFFFAOYSA-N amino(oxo)methanesulfinic acid Chemical compound NC(=O)S(O)=O MDHRKTMFBQWLPG-UHFFFAOYSA-N 0.000 description 1
- BTBJBAZGXNKLQC-UHFFFAOYSA-N ammonium lauryl sulfate Chemical compound [NH4+].CCCCCCCCCCCCOS([O-])(=O)=O BTBJBAZGXNKLQC-UHFFFAOYSA-N 0.000 description 1
- 229940063953 ammonium lauryl sulfate Drugs 0.000 description 1
- 229940027983 antiseptic and disinfectant quaternary ammonium compound Drugs 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 229940075506 behentrimonium chloride Drugs 0.000 description 1
- 229960003872 benzethonium Drugs 0.000 description 1
- 238000004061 bleaching Methods 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Chemical class [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 1
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical class OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 1
- 150000003842 bromide salts Chemical class 0.000 description 1
- 239000002738 chelating agent Substances 0.000 description 1
- 229960004106 citric acid Drugs 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 239000006184 cosolvent Substances 0.000 description 1
- 150000001945 cysteines Chemical class 0.000 description 1
- 238000004042 decolorization Methods 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical class OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- IZFHEQBZOYJLPK-UHFFFAOYSA-N dihydrolipoic acid Chemical compound OC(=O)CCCCC(S)CCS IZFHEQBZOYJLPK-UHFFFAOYSA-N 0.000 description 1
- SIYLLGKDQZGJHK-UHFFFAOYSA-N dimethyl-(phenylmethyl)-[2-[2-[4-(2,4,4-trimethylpentan-2-yl)phenoxy]ethoxy]ethyl]ammonium Chemical compound C1=CC(C(C)(C)CC(C)(C)C)=CC=C1OCCOCC[N+](C)(C)CC1=CC=CC=C1 SIYLLGKDQZGJHK-UHFFFAOYSA-N 0.000 description 1
- REZZEXDLIUJMMS-UHFFFAOYSA-M dimethyldioctadecylammonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CCCCCCCCCCCCCCCCCC REZZEXDLIUJMMS-UHFFFAOYSA-M 0.000 description 1
- GVGUFUZHNYFZLC-UHFFFAOYSA-N dodecyl benzenesulfonate;sodium Chemical compound [Na].CCCCCCCCCCCCOS(=O)(=O)C1=CC=CC=C1 GVGUFUZHNYFZLC-UHFFFAOYSA-N 0.000 description 1
- 238000004043 dyeing Methods 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- DNJIEGIFACGWOD-UHFFFAOYSA-N ethanethiol Chemical compound CCS DNJIEGIFACGWOD-UHFFFAOYSA-N 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 229940013688 formic acid Drugs 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 229940097043 glucuronic acid Drugs 0.000 description 1
- 229960004275 glycolic acid Drugs 0.000 description 1
- 229940093915 gynecological organic acid Drugs 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- 231100001261 hazardous Toxicity 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N hydrogen thiocyanate Natural products SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229960000448 lactic acid Drugs 0.000 description 1
- 229940075468 lauramidopropyl betaine Drugs 0.000 description 1
- 229940094506 lauryl betaine Drugs 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 229940099690 malic acid Drugs 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 229960002510 mandelic acid Drugs 0.000 description 1
- 239000000463 material Substances 0.000 description 1
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 1
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical compound CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 description 1
- 229910017604 nitric acid Inorganic materials 0.000 description 1
- 230000000269 nucleophilic effect Effects 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 229940116315 oxalic acid Drugs 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000006174 pH buffer Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- ACVYVLVWPXVTIT-UHFFFAOYSA-N phosphinic acid Chemical compound O[PH2]=O ACVYVLVWPXVTIT-UHFFFAOYSA-N 0.000 description 1
- 229920000136 polysorbate Chemical class 0.000 description 1
- 229950008882 polysorbate Drugs 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 238000001055 reflectance spectroscopy Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- WXMKPNITSTVMEF-UHFFFAOYSA-M sodium benzoate Chemical compound [Na+].[O-]C(=O)C1=CC=CC=C1 WXMKPNITSTVMEF-UHFFFAOYSA-M 0.000 description 1
- 239000004299 sodium benzoate Substances 0.000 description 1
- 235000010234 sodium benzoate Nutrition 0.000 description 1
- XUXNAKZDHHEHPC-UHFFFAOYSA-M sodium bromate Chemical compound [Na+].[O-]Br(=O)=O XUXNAKZDHHEHPC-UHFFFAOYSA-M 0.000 description 1
- 229940080264 sodium dodecylbenzenesulfonate Drugs 0.000 description 1
- 229940057950 sodium laureth sulfate Drugs 0.000 description 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 description 1
- MDSQKJDNWUMBQQ-UHFFFAOYSA-M sodium myreth sulfate Chemical compound [Na+].CCCCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O MDSQKJDNWUMBQQ-UHFFFAOYSA-M 0.000 description 1
- 239000001488 sodium phosphate Substances 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- SXHLENDCVBIJFO-UHFFFAOYSA-M sodium;2-[2-(2-dodecoxyethoxy)ethoxy]ethyl sulfate Chemical compound [Na+].CCCCCCCCCCCCOCCOCCOCCOS([O-])(=O)=O SXHLENDCVBIJFO-UHFFFAOYSA-M 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-N sulfurothioic S-acid Chemical compound OS(O)(=O)=S DHCDFWKWKRSZHF-UHFFFAOYSA-N 0.000 description 1
- 229960001367 tartaric acid Drugs 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- ISIJQEHRDSCQIU-UHFFFAOYSA-N tert-butyl 2,7-diazaspiro[4.5]decane-7-carboxylate Chemical compound C1N(C(=O)OC(C)(C)C)CCCC11CNCC1 ISIJQEHRDSCQIU-UHFFFAOYSA-N 0.000 description 1
- 150000005621 tetraalkylammonium salts Chemical class 0.000 description 1
- ZMZDMBWJUHKJPS-UHFFFAOYSA-M thiocyanate group Chemical group [S-]C#N ZMZDMBWJUHKJPS-UHFFFAOYSA-M 0.000 description 1
- 229940035024 thioglycerol Drugs 0.000 description 1
- RYFMWSXOAZQYPI-UHFFFAOYSA-K trisodium phosphate Chemical compound [Na+].[Na+].[Na+].[O-]P([O-])([O-])=O RYFMWSXOAZQYPI-UHFFFAOYSA-K 0.000 description 1
- 229910000406 trisodium phosphate Inorganic materials 0.000 description 1
- 235000019801 trisodium phosphate Nutrition 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
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
- A61K8/31—Hydrocarbons
-
- 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
-
- 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
- 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
- A61K2800/80—Process related aspects concerning the preparation of the cosmetic composition or the storage or application thereof
- A61K2800/88—Two- or multipart kits
- A61K2800/882—Mixing prior to application
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)
- Cosmetics (AREA)
Abstract
Claimed is an alkaline colour removal composition comprising: a) formamidine sulfinic acid (thiourea dioxide); b) an inert hydrophobic liquid; c) urea; and d) a sulfur containing nucleophile. Most preferably, the inert hydrophobic liquid is liquid paraffin. Most preferably, the sulfur containing nucleophile is thioglycolic acid. Preferably, the composition has a pH of 9 to 10. Also claimed is a kit of parts wherein components a) and b) form a first precursor and c) and d) form a second precursor. Further claimed is a method of removing color from dyed hair (i.e. a keratin fibre) wherein components A)-D) are mixed; the composition comprising A)-D) is contacted with the hair; subsequently, an oxidizing composition (e.g. hydrogen peroxide) is added to the hair. Inventive concept is the inclusion of paraffin liquid into a hair decolouring composition comprising formamidine sulphinic acid, urea and sulfur containing nucleophile.
Description
(54) Title of the Invention: Hair treatments
Abstract Title: Hair bleaching/decolouring composition comprising: formamidine sulfinic acid; inert hydrophobic liquid; urea; a sulfur containing nucleophile (57) Claimed is an alkaline colour removal composition comprising: a) formamidine sulfinic acid (thiourea dioxide); b) an inert hydrophobic liquid; c) urea; and d) a sulfur containing nucleophile. Most preferably, the inert hydrophobic liquid is liquid paraffin. Most preferably, the sulfur containing nucleophile is thioglycolic acid. Preferably, the composition has a pH of 9 to 10. Also claimed is a kit of parts wherein components a) and b) form a first precursor and c) and d) form a second precursor. Further claimed is a method of removing color from dyed hair (i.e. a keratin fibre) wherein components A)-D) are mixed; the composition comprising A)-D) is contacted with the hair; subsequently, an oxidizing composition (e.g. hydrogen peroxide) is added to the hair. Inventive concept is the inclusion of paraffin liquid into a hair decolouring composition comprising formamidine sulphinic acid, urea and sulfur containing nucleophile.
Mins
Figure 4
1811
1/4
Figure 1B
Figure 2
3/4
Mins mins
Mins
Figure 3
4/4
Mins
Mins
Mins
Figure 4
Hair treatments
The present invention relates to compositions and methods for the removal of colour from dyed materials, in particular for the removal of colour from dyed hair, especially human hair.
There are a number of existing compositions for removing colour from hair which has been dyed. However many of these are unsatisfactory. For example the compositions may cause damage to the hair; the chemicals used in some prior art compositions are hazardous to health; and in many cases the result achieved is incomplete or inconsistent. The time taken to achieve colour removal is also an important consideration.
It is an aim of the present invention to provide a colour removal composition which can be used to efficiently and safely remove colour from dyed hair with a high degree of reproducibility.
According to the first aspect of the present invention there is provided an alkaline colour removal composition comprising:
a) formamidine sulfinic acid;
b) an inert hydrophobic liquid;
c) urea; and
d) a sulfur containing nucleophile.
Component (a) comprises formamidine sulfinic acid. This compound has the following formula:
O
H2N
OH
NH
It is believed that formamidine sulfinic acid hydrolyses to form the nucleophilic species HSO2 (hydrosulfoxylate).
An advantage of using formamidine sulfinic acid is that, unlike other sources of hydrosulfoxylate, it does not produce formaldehyde during use.
It is known from the prior art to use aminomethanesulfinic acid for colour removal. Under the conditions of use this compound was not very effective. However for the avoidance of doubt, the compositions of the present invention do not comprise aminomethanesulfinic acid.
The composition of the present invention preferably comprises at least 0.1 wt% formamidine sulfinic acid, preferably at least 0.5 wt%, more preferably at least 1 wt%, preferably at least 1.5 wt%, preferably at least 2 wt%, suitably at least 2.5 wt%, for example at least 3 wt% or at least 4 wt%.
Suitably the composition comprises up to 30 wt% formamidine sulfinic acid, preferably up to 15 wt%, suitably up to 10 wt%, preferably up to 8 wt%, more preferably up to 7 wt%, for example up to 6 wt% or up to 5 wt%.
Component (b) is an inert hydrophobic liquid. Suitable components of this type include mixtures of hydrocarbons and silicone oils.
Preferably component (b) comprises paraffin liquid.
The composition of the present invention preferably comprises at least 0.1 wt% paraffin liquid, preferably at least 0.5 wt%, more preferably at least 1 wt%, preferably at least 1.5 wt%, preferably at least 2 wt%, suitably at least 2.5 wt%, for example at least 3 wt% or at least 4 wt%.
Suitably the composition comprises up to 30 wt% paraffin liquid, preferably up to 15 wt%, suitably up to 10 wt%, preferably up to 8 wt%, more preferably up to 7 wt%, for example up to 6 wt% or up to 5 wt%.
The weight ratio of component (a) to component (b) is preferably from 10:1 to 1:10, preferably from 5:1 to 1:5, more preferably from 2:1 to 1:2, for example about 1:1.
Component (c) comprises urea. The urea is preferably present in the composition of the present invention an amount of at least 0.1 wt%, suitably at least 1wt%, more preferably at least 2.5 wt%, suitably at least 5 wt%, preferably at least 10 wt%, more preferably at least 12.5%, for example at least 15 wt%.
The composition preferably comprises up to 50wt% urea, suitably up to 40wt%, more preferably up to 30wt%, suitably up to 25 wt%, for example up to 20wt%.
Component (d) comprises a sulfur-containing nucleophile. Suitably the sulfur containing nucleophile is not formamidine sulfinic acid and is present in addition to this.
Preferably the sulfur-containing nucleophile is selected from thiocyanate, sulfite salts (eg sodium sulfite), thioglycolic acid, thiocarbamate, carbamoylsulfinic acid, thioethanol, thiolactic acid, dihydrolipoate, thioglycerol, mercaptopropionic acid, cysteine, N-substituted cysteine, cysteamines, N-substituted cysteamines, thiosulfate, 1-thiopropane-3-sulfonate and mixtures and/or salts thereof.
In especially preferred embodiments component (d) comprises thioglycolic acid.
The sulfur-containing nucleophile is suitably present in the composition of the present invention in an amount of at least 0.1 wt%, preferably at least 0.25 wt%, more preferably at least 0.5 wt%, suitably at least 0.8 wt%, preferably at least 1 wt%.
The composition of the present invention suitably comprises up to 20 wt% of the sulfur containing nuclephile, preferably up to 10 wt%, more preferably up to 5 wt%, preferably up to 3 wt%, for example up to 2 wt%.
The composition of the present invention is preferably an aqueous composition. Suitably it comprises at least 30 wt% water, suitably at least 40 wt%, preferably at least 50 wt%, more preferably at least 55 wt%, for example at least 60 wt%.
The composition may comprise up to 95 wt% water, suitably up to 90 wt%, preferably up to 80 wt%, for example up to 70 wt%.
The composition of the present invention may further comprise one or more ingredients selected from surfactants, emulsifiers, colourants, fragrances, buffers, solvents, thickening agents and conditioning agents.
In some embodiments the composition further comprises one or more water miscible solvents, for example monohydric and polyhydric alcohols.
One especially preferred additional solvent is glycerol. Glyercol is suitably present in the composition in an amount of from 0.1 to 20 wt%, preferably 0.5 to 10 wt%, more preferably from 1 to 5 wt%, for example from 2 to 4 wt%.
The composition of the present invention is an alkaline composition. Suitably it has a pH of at least 7.5, preferably at least 8.
Suitably the composition of the present invention has a pH of from 8 to 11, preferably from 9 to 10.
The composition may include a buffer. Suitable pH buffers include 2-amino-2-methyl-1propanol. Other suitable buffers will be known to the person skilled in the art.
The buffer may suitably be present in an amount of from 0.1 to 5 wt%, for example from 1 to 3 wt%.
In some preferred embodiments the composition comprises one or more surfactants. Any suitable surfactant or mixture of surfactants may be included, for example anionic, cationic, amphoteric or nonionic surfactants. Suitable surfactants will be known to the person skilled in the art. Nonionic surfactants are especially preferred.
Suitable non-ionic surfactants will be known to the person skilled in the art. Preferred nonionic surfactants are alkoxyiated compounds, for example ethoxylated and polyethoxylated surfactants. One especially preferred non-ionic surfactant used herein is polysorbate 80.
The composition of the present invention suitably comprises from 0.1 to 20 wt% non-ionic surfactants, preferably from 0.5 to 10 wt%, more preferably from 1 to 5 wt%.
The composition may include a thickener. Suitable thickeners will be known to the person skilled in the art. Preferred thickeners are non-ionic thickeners. One suitable thickener is hydroxyethylcellulose.
Preferably the composition of the present invention comprises from 0.1 to 20 wt%, preferably from 0.25 to 10 wt%, more preferably from 0.5 to 2.5 wt% of thickeners.
The composition of the present invention may further comprise a quaternary ammonium compound. Suitable quaternary ammonium compounds are known to the person skilled in the art and include cetyl trimethyl ammonium chloride. This is suitably present in amount of from 0.01 to 0.5 wt% preferably from 0.1 to 0.25 wt%.
Suitably the colour removal composition of the present invention comprises:
(a) from 0.1 to 20 wt%, preferably from 1 to 10 wt% of formamidine sulfinic acid;
(b) from 0.1 to 20 wt%, preferably from 1 to 10 wt% of paraffin liquid;
(c) from 0.1 to 50 wt%, preferably from 10 to 20 wt% of urea; and (d) from 0.1 to 10 wt%, preferably from 0.5 to 3 wt% of thioglycolic acid.
In some embodiments the composition further comprises glycerol and polysorbate 80.
The composition of the present invention is suitably in the form of a gel, paste or viscous liquid. It suitably has a consistency of a shampoo or conditioning composition enabling it to be applied to and spread throughout the hair without running off.
The composition of the present invention may prepared shortly prior to use by admixture of two precursor compositions.
According to a second aspect of the present invention there is provided a colour removal kit comprising:
(i) a first precursor composition comprising:
(a) formamidine sulfinic acid; and (b) an inert hydrophobic liquid; and (ii) a second precursor composition comprising:
(c) urea; and (d) a sulfur containing nucleophile.
Suitably admixture of the first precursor composition and the second precursor composition provides a colour removal composition of the first aspect.
Preferred features of the second aspect are as defined in relation to the first aspect.
The first precursor composition comprises component (a) and component (b). Preferably component (a) and component (b) together comprise at least 50 wt% of the first precursor composition, preferably at least 70 wt%, more preferably at least 90 wt%, preferably least 95 wt%.
Preferably the first precursor composition consists essentially of component (a) and component (b).
Thus the first precursor composition suitably consists essentially of formamidine sulfinic acid and paraffin liquid.
These are suitably present in weight ratio of from 3:1 to 1:3, preferably about 1:1. The first precursor composition suitably has the appearance of a “wet” power.
The second precursor composition comprises urea and a sulfur containing nucleophile.
The sulfur containing nucleophile is suitably present in the second precursor composition in an amount of from 0.1 to 10 wt%, preferably 0.5 to 5 wt%, more preferably 1 to 2 wt%.
The second precursor composition preferably comprises 1 to 40 wt% urea, preferably 10 to 30 wt%, more preferably 15 to 25 wt%.
The second precursor composition is preferably an aqueous composition. Preferably it is the form of a gel or paste.
The second precursor composition preferably comprises from 50 to 95 wt% water, preferably 55 to 90 wt%, more preferably from 60 to 80 wt%.
The second precursor composition preferably further comprises glycerol, in an amount of from 0.1 to 10 wt% preferably from 1 to 5 wt%.
The second precursor composition preferably further comprises a non-ionic surfactant, for example polysorbate 80, preferably in an amount of from 0.1 to 10 wt%, suitably 1 to 5 wt%.
The second precursor composition may further comprise a quaternary ammonium salt, a thickener and a fragrance.
Preferably admixture of the first precursor composition and the second precursor composition provides a substantially homogeneous composition.
Preferably the first precursor composition and the second precursor composition are mixed in a ratio (by weight) of from 100:1 to 1:1, preferably from 50:1 to 2:1, more preferably from 20:1 to 5:1, suitably from 15:1 to 8:1, for example about 10:1.
According to a third aspect of the invention there is provided a method of removing colourfrom dyed hair, the method comprising contacting the hair with an alkaline composition comprising:
a)
b)
c) formamidine sulfinic acid; an inert hydrophobic liquid; urea; and
d) a sulfur containing nucleophile.
Suitably the method of the third aspect involves contacting the hair with a colour removal composition of the first aspect. Preferred features of the third aspect are as defined in relation to the first and second aspects.
Suitably in the method of the present invention the colour removal composition is applied to the hair, spread throughout the hair and left on the hair for at least 0.1 mins.
The composition may be applied to the hair by any suitable means. It may be applied using a brush or other implement of by hand. Suitably it is brushed on to the hair to provide an even coverage. Suitably the colour removal composition is contacted with the hair using a liquor ratio of from 5:1 to 1:1, preferably from 4:1 to 3:1, suitably about 2.5:1. By this we mean that 2.5 parts by weight of the composition is applied for each part by weight of hair used.
Suitably once the composition has been applied the hair is covered by a cap to prevent evaporation.
Suitably the colour removal composition is left on the hair for a period of at least 1 min, preferably at least 5 min, more preferably at least 10 min, for example at least 15 min or at least 20 min.
The colour removal composition may be left on the hair for up to 4 hours, suitably up to 3 hours, preferably up to 2 hours, for example up to 1.5 hours.
Preferably the colour removal composition is left on the hair for a period of 30 to 60 minutes.
The time for which the composition should be left in contact with the hair will depend on the starting colour of the hair. For hair that has been dyed with a light colour, colour removal can usually be achieved within 10 to 20 minutes. For black hair up to 60 minutes may be needed. The extent of the colour removal can be monitored by visual inspection.
Suitably the colour removal composition is applied to the hair and maintained on the head at a temperature of from 10 to 75 °C, preferably from 20 to 60 °C, more preferably from 30 to 50 °C.
When using temperatures above ambient temperature a suitable hood can be employed to achieve the required temperature.
The colour removal composition is then suitably rinsed from the hair.
Preferably the hair is then contacted with a oxidising composition.
In preferred embodiments the method of the third aspect involves the steps:
(x) preparing an alkaline colour removal composition comprising:
a) formamidine sulfinic acid;
b) an inert hydrophobic liquid;
c) urea; and
d) a sulfur containing nucleophile;
(y) contacting the hair with the colour removal composition; and (z) contacting the hair with an oxidising composition.
Suitably there is a step between step (y) and step (z) of rinsing the hair with water.
The oxidising composition may comprise any suitable oxidising agent. Preferred oxidising agents include bromate salts and peroxides. Suitable bromates include sodium bromate. Suitable peroxides include hydrogen peroxide.
Preferably the oxidising composition comprises hydrogen peroxide.
Preferably the oxidising composition comprises at least 0.01 wt% hydrogen peroxide, more preferably at least 0.05 wt%, suitably at least 0.1 wt%, for example at least 0.3 wt% or at least 0.5 wt%.
The composition may comprise up to 10 wt% hydrogen peroxide, suitably up to 7.5 wt%, preferably up to 5 wt%, suitably up to 3 wt%, for example up to 2 wt% or up to 1 wt%..
The oxidising composition is preferably an acidic composition.
The oxidising composition preferably has a pH of from 1 to 6.5, more preferably from 2 to 6, more preferably from 3 to 5, for example from 3 to 4 or from 3 to 3.5.
Suitable acids that may be included in the oxidising composition include organic and inorganic acids. Suitable organic acids include ascorbic acid, acetic acid, oxalic acid, lactic acid, formic acid, citric acid, glycolic acid, glucuronic acid, malic acid, mandelic acid, salicylic acid and tartaric acid.
Suitable inorganic acids include hydrochloric acid, sulfuric acid, nitric acid, phosphorous acid, hypophosphorous acid and phosphoric acid.
In especially preferred embodiments the oxidising composition comprises salicylic acid.
The acid is suitably present in an amount of from 0.01 to 3 wt%, preferably 0.1 to 1 wt%.
The oxidising composition preferably further comprises one or more surfactants. Suitable surfactants will be known to the person skilled in art and include anionic, cationic, non-ionic and amphoteric surfactants. Mixtures of surfactants may be present.
Suitable anionic surfactants for use herein include sulfate and sulfonate compounds including an alkyl or alkylene chain typically of 8 to 30 carbon atoms, preferably provided as an alkali metal or ammonium salt. Substituted ammonium salts may be used, for example tetraalkyl ammonium salts. Examples of suitable anionic surfactants include ammonium lauryl sulfate, alkyl ammonium lauryl sulfates, sodium lauryl sulfate, sodium laureth sulfate, sodium myreth sulfate and sodium dodecyl benzene sulfonate.
Suitable amphoteric surfactants include betaines and sultaines. Suitable betaines include alkyl betaines, for example cetyl betaine, lauryl betaine, stearyl betaine and behenyl betaine. Examples of suitable amphoteric surfactants include cocoamido propyl betaine, lauramido propyl betaine, cocamidopropyl hydroxysultaine and lauryl hydroxysultaine.
Suitable cationic surfactants for use herein include quaternary ammonium salts including one or more long alkyl or alkenyl chain typically of 8 to 30 carbon atoms, preferably provided as a chloride or bromide salt. Examples of suitable cationic surfactants include benzethonium trimethyl ammonium chloride, dimethyl dioctadecyl ammonium chloride, cetyl trimethyl ammonium chloride, stearyl trimethyl ammonium chloride and beheneth trimethyl ammonium chloride.
Suitable non-ionic surfactants for use herein include alkoxylated and polyalkoxylated compounds and fatty acids, fatty alcohols and fatty amines including one or more hydroxy alkyl substituents. Examples of suitable non-ionic surfactants include cocamide monoethanolamine, cocamide diethanolamine and polysorbate compounds. Preferred non-ionic surfactants are fatty alcohols and ethoxylated fatty alcohols, for example cetyl alcohol and stearyl alcohol.
Preferably the oxidising composition comprises a mixture of non ionic and cationic surfactants. Preferred surfactants for use in the oxidising composition include cetyl trimethyl ammonium chloride, behenyl trimethyl ammonium chloride, stearyl alcohol, cetyl alcohol ceterath-25.
In preferred embodiments the oxidising composition comprises from 0.1 to 15 wt%, preferably 2 to 8 wt% surfactants.
The oxidising composition may comprise one or more further ingredients, for example those typically found in shampoo compositions. Such ingredients include surfactants, thickeners, fragrances, colourants, preservatives, conditioning agents, cosolvents and chelating agents. Examples of such ingredients may be found on the INCI list.
The oxidising composition is preferably an aqueous composition. Suitably it comprises 50 to 99.9 wt% water. It may comprise from 70 to 99 wt%, suitably 80 to 98 wt% water. Preferably it comprises from 85 to 95 wt% water.
The oxidising composition is preferably in the form of a viscous liquid or gel. It suitably has a consistency similar to that of shampoo and is used in a similar manner.
Suitably the oxidising composition is liberally applied to the hair and spread thoroughly throughout the hair. This may be done manually using the fingers as one might spread shampoo throughout the hair. Alternatively it may be applied using a brush.
Preferably after application of the oxidising composition it is allowed to remain in contact with the hair for a period of at least 30 seconds, suitably at least 1 minute, preferably at least 2 minutes, preferably at least 3 minutes, for example at least 4 minutes. The oxidising composition may be allowed to remain in contact with the hair for up to 20 minutes, suitably up to 15 minutes, preferably up to 10 minutes, more preferably up to 8 minutes, for example up to 6 minutes.
Step (z) may suitably be carried out at ambient temperature. However it has been observed to be more efficient at higher temperatures.
Following step (z) the composition may be rinsed from the hair, for example with warm water.
In some preferred embodiments step (z) is repeated.
Hair treated according to the present invention suitably has a colour that closely matches its colour prior to dyeing. In the case of a very strong colour or if the hair is very porous, the method may be repeated.
The present invention may be used to remove colour from hair that has been dyed using variety of different classes of hair dyes. For example the invention can very effectively remove colour from hair dyed using the compounds and methods described in the applicant’s applications WO 2010/032034 and WO 2009/112858. Furthermore the present invention also reliably removes colour from hair that has been oxidatively dyed and does not cause significant damage to the hair or use dangerous chemicals.
It has been surprisingly found that the inclusion of paraffin liquid in the colour removal composition provides a more homogeneous composition and faster colour removal.
According to a fourth aspect of the present invention there is provided a packaged hair colour removal product comprising:
(i) a first precursor composition comprising:
(a) formamidine sulfinic acid; and (b) an inert hydrophobic liquid; and (ii) a second precursor composition comprising:
(c) urea; and (d) a sulfur containing nucleophile; and (iii) a oxidising composition.
Components (i), (ii) and (iii) may suitably be included in the packaged hair colour removal product in unit dose form. Thus in some preferred embodiments the packaged hair colour removal product of the present invention comprises components (i), (ii) and (iii) in an amount sufficient for use in a single colour removal event, for example to remove colour from a single head of human hair.
Suitably the packaged hair colour removal product further comprises instructions for using the compositions. The product may comprise further components, for example a disposable cap. It may optionally include apparatus for mixing the compositions and or applying to the head. For example it may include a mixing bowl, spoon, spatula, brush or disposable gloves.
Compositions (i), (ii) and (iii) are included in the kit in suitable packaging. They are suitably packaged separately. Any suitably packaging may be used and suitable packing will be known to the person skilled in the art.
The compositions may be packaged in bottles, jars, tubes, sachets or boxes. The packaging or each composition may be the same or different. In some embodiments one or more of the compositions may be packaged in an inert atmosphere, or in a vacuum.
Suitably the product of the fourth aspect comprises an outer packaging. The packaged colour removal product suitably contains all components necessary for a single colour removal event, for example the removal of colour from a single head of hair.
According to a fifth aspect of the present invention there is provided the use of an alkaline composition comprising:
a) formamidine sulfinic acid;
b) an inert hydrophobic liquid;
c) urea; and
d) a sulfur containing nucleophile; to remove colour from dyed hair.
The invention will now be further described with reference to the following non-limiting examples.
Example
A first precursor composition was prepared comprising the following components:
| Ingredient | %w/w |
| Formamidine sulfinic acid | 50 |
| Paraffin liquid | 50 |
A second precursor composition was prepared comprising the following components:
| Ingredient | %w/w |
| Water | 69.7 |
| urea | 19.1 |
| Glycerin | 3.0 |
| polysorbate 80 | 2.9 |
| Aminomethylpropanol | 1.9 |
| hydroxyethylcellulose | 1.3 |
| thioglycolic acid | 1.4 |
| parfum | 0.5 |
| Cetrimonium chloride | 0.2 |
A comparative first precursor composition comprising only formamidine sulfinic acid was also prepared.
The first and second precursor compositions were mixed in a ratio of 1:10 by weight (first precursor composition : second precursor composition) to provide a colour removal gel.
A comparative colour removal composition was also prepared using the comparative precursor composition.
Figure 1A shows the comparative composition and Figure 1B shows the composition of the invention.
Figure 2 shows the comparative composition on the left and inventive composition on the right.
It can be clearly seen that the composition of the invention is homogenous whereas the comparative is not.
These compositions were applied to hair tresses that had been dyed using a Majirel 1 dye. As the photographs in Figure 3 illustrate (left pictures inventive, right pictures comparative), the compositions of the invention gave faster colour removal.
As the colour difference can be difficult to see in black and white photographs, the colour was measured using reflectance spectrometry. The values were measured according to the “CIE L*a*b*’ or CIELAB system. This system will be known to the person skilled in the art. The results for the hair tresses shown in figure 3 are given in table 1.
It should be noted that a higher value for L* indicates a lighter colour of hair and therefore greater decolourisation.
Table 1
| Time (mins) | With Paraffin | Without paraffin | ||||
| L* | a* | b* | L* | a* | b* | |
| 0 | 30.514 | 1.054 | -5.012 | 30.97 | 0.72 | -5.548 |
| 10 | 34.32 | 2.624 | -2.032 | 30.684 | 0.742 | -5.912 |
| 20 | 38.494 | 1.71 | 0.374 | 33.106 | 1.978 | -3.602 |
| 30 | 43.588 | 1.14 | 3.632 | 35.312 | 1.788 | -1.83 |
| 40 | 42.494 | 1.82 | 7.092 | 38.006 | 1.71 | 1.144 |
| 50 | 44.42 | 3.148 | 10.214 | 41.826 | 3.716 | 7.806 |
| 60 | 52.65 | 7.934 | 21.208 | 47.67 | 6.376 | 14.848 |
The experiment was repeated using hair dyed using a Majirel 5 dye. The results are shown in Figure 4 and table 2.
Table 2
| Time (mins) | With Paraffin | Without paraffin | ||||
| L* | a* | b* | L* | a* | b* | |
| 10 | 47.496 | 0.702 | 3.702 | 46.898 | 0.296 | 1.242 |
| 20 | 55.404 | 1.216 | 13.482 | 54.016 | 0.22 | 8.292 |
| 30 | 61.294 | 4.37 | 21.684 | 59.066 | 1.89 | 14.494 |
| 40 | 62.368 | 3.326 | 23.36 | 60.85 | 3.538 | 19.522 |
A oxidising composition having the formula below was applied to the hair after rinsing.
| Ingredient | %w/w |
| water | 91.5 |
| cetyl alcohol | 2.0 |
| stearyl alcohol | 2.0 |
| Behentrimonium chloride | 1.0 |
| hydrogen peroxide | 0.8 |
| ceteareth-25 | 0.8 |
| Cetrimonium chloride | 0.3 |
| sodium benzoate | 0.3 |
| EDTA | 0.3 |
| salicylic acid | 0.3 |
| Isopropyl alcohol | 0.3 |
| trisodium phosphate | 0.2 |
| etidronic acid | 0.2 |
Claims (10)
1. An alkaline colour removal composition comprising:
a) formamidine sulfinic acid;
b) an inert hydrophobic liquid;
c) urea; and
d) a sulfur containing nucleophile.
2. A composition according to claim 1 wherein the inert hydrophobic liquid is paraffin liquid.
3. A composition according to claim 1 or claim 2 wherein the sulfur containing nucleophile is thioglycolic acid.
4. A composition according to any preceding claim which has a pH of 9 to 10.
5. A colour removal kit comprising:
(i) a first precursor composition comprising:
(a) formamidine sulfinic acid; and (b) an inert hydrophobic liquid; and (ii) a second precursor composition comprising:
(c) urea; and (d) a sulfur containing nucleophile.
6. A method of removing colour from dyed hair, the method comprising contacting the hair with an alkaline composition comprising:
a)
b)
c)
d) formamidine sulfinic acid; an inert hydrophobic liquid; urea; and a sulfur containing nucleophile.
7. A method according to claim 6 which involves the steps of:
(x) preparing an alkaline colour removal composition comprising:
a) formamidine sulfinic acid;
b) an inert hydrophobic liquid;
c) urea; and
d) a sulfur containing nucleophile;
(y) contacting the hair with the colour removal composition; and (z) contacting the hair with a oxidising composition.
8. A method according to claim 7 wherein there is a step between step (y) and step (z) of rinsing the hair with water.
9. The use of an alkaline composition comprising:
a) formamidine sulfinic acid;
b) paraffin liquid;
c) urea; and
d) a sulfur containing nucleophile; to remove colour from dyed hair.
Intellectual
Property
Office
Application No: GB1711291.3 Examiner: Mr Robert Goodwill
9. A packaged hair colour removal product comprising:
(i) a first precursor composition comprising:
(a) formamidine sulfinic acid; and (b) an inert hydrophobic liquid; and (ii) a second precursor composition comprising:
(c) urea; and (d) a sulfur containing nucleophile; and (iii) a oxidising composition.
10. The use of an alkaline composition comprising:
a) formamidine sulfinic acid;
b) an inert hydrophobic liquid;
c) urea; and
d) a sulfur containing nucleophile; to remove colour from dyed hair.
Amendments to the claims have been filed as follows:
Claims
1. An alkaline colour removal composition comprising:
a)
b)
c)
d) formamidine sulfinic acid; paraffin liquid; urea; and a sulfur containing nucleophile;
25 04 18 wherein the weight ratio of component (a) to component (b) is from 2:1 to 1:2.
2. A composition according to claim 1 wherein the sulfur containing nucleophile is thioglycolic acid.
3. A composition according to claim 1 or claim 2 which has a pH of 9 to
10.
4. A colour removal kit comprising:
(i) a first precursor composition comprising:
(a) formamidine sulfinic acid; and (b) paraffin liquid; and (ii) a second precursor composition comprising:
(c) urea; and (d) a sulfur containing nucleophile;
wherein the weight ratio of component (a) to component (b) is from 2:1 to 1:2.
5. A method of removing colour from dyed hair, the method comprising contacting the hair with an alkaline composition comprising:
a)
b)
c)
d) formamidine sulfinic acid; paraffin liquid; urea; and a sulfur containing nucleophile.
6. A method according to claim 5 which involves the steps of:
(x) preparing an alkaline colour removal composition comprising:
a) formamidine sulfinic acid;
b) paraffin liquid;
c) urea; and
d) a sulfur containing nucleophile;
(y) contacting the hair with the colour removal composition; and (z) contacting the hair with an oxidising composition.
7. A method according to claim 6 wherein there is a step between step (y) and step (z) of rinsing the hair with water.
8. A packaged hair colour removal product comprising:
(i) a first precursor composition comprising:
(a) formamidine sulfinic acid; and (b) paraffin liquid; and
25 04 18 (ii) a second precursor composition comprising:
(c) urea; and (d) a sulfur containing nucleophile; and (iii) an oxidising composition;
wherein the weight ratio of component (a) to component (b) is from 2:1 to 1:2.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB1612513.0A GB201612513D0 (en) | 2016-07-19 | 2016-07-19 | Hair treatments |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| GB201711291D0 GB201711291D0 (en) | 2017-08-30 |
| GB2557383A true GB2557383A (en) | 2018-06-20 |
| GB2557383B GB2557383B (en) | 2019-01-23 |
Family
ID=56890638
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GBGB1612513.0A Ceased GB201612513D0 (en) | 2016-07-19 | 2016-07-19 | Hair treatments |
| GB1711291.3A Expired - Fee Related GB2557383B (en) | 2016-07-19 | 2017-07-13 | Hair treatments |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GBGB1612513.0A Ceased GB201612513D0 (en) | 2016-07-19 | 2016-07-19 | Hair treatments |
Country Status (2)
| Country | Link |
|---|---|
| GB (2) | GB201612513D0 (en) |
| WO (1) | WO2018015721A1 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE102017204290A1 (en) * | 2017-03-15 | 2018-09-20 | Henkel Ag & Co. Kgaa | Means for discoloring dyed keratinic fibers |
| WO2024115456A1 (en) * | 2022-11-29 | 2024-06-06 | Kao Corporation | Discoloring composition for keratin fibers dyed with oxidative dyes or direct dyes |
Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1287699A (en) * | 1961-03-31 | 1962-03-16 | Solution to give permanent waves to hair | |
| GB2493207A (en) * | 2011-07-29 | 2013-01-30 | Perachem Ltd | Method of removing oxidative hair dye from hair |
| GB2513319A (en) * | 2013-04-22 | 2014-10-29 | Perachem Ltd | Hair treatment kit |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2103683C (en) * | 1992-08-17 | 1998-06-16 | George Weeks | Methods of controlling dust and compositions produced thereby |
| WO2009112858A2 (en) | 2008-03-10 | 2009-09-17 | Perachem Limited | Hair treatment composition and methods |
| CN102159175A (en) | 2008-09-16 | 2011-08-17 | 佩拉化学有限公司 | Hair Treatment |
-
2016
- 2016-07-19 GB GBGB1612513.0A patent/GB201612513D0/en not_active Ceased
-
2017
- 2017-07-13 WO PCT/GB2017/052072 patent/WO2018015721A1/en not_active Ceased
- 2017-07-13 GB GB1711291.3A patent/GB2557383B/en not_active Expired - Fee Related
Patent Citations (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR1287699A (en) * | 1961-03-31 | 1962-03-16 | Solution to give permanent waves to hair | |
| GB2493207A (en) * | 2011-07-29 | 2013-01-30 | Perachem Ltd | Method of removing oxidative hair dye from hair |
| GB2513319A (en) * | 2013-04-22 | 2014-10-29 | Perachem Ltd | Hair treatment kit |
Also Published As
| Publication number | Publication date |
|---|---|
| GB201612513D0 (en) | 2016-08-31 |
| GB2557383B (en) | 2019-01-23 |
| GB201711291D0 (en) | 2017-08-30 |
| WO2018015721A1 (en) | 2018-01-25 |
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| Date | Code | Title | Description |
|---|---|---|---|
| 732E | Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977) |
Free format text: REGISTERED BETWEEN 20211118 AND 20211124 |
|
| PCNP | Patent ceased through non-payment of renewal fee |
Effective date: 20240713 |









