ZA200300250B - Method of treating hair. - Google Patents
Method of treating hair. Download PDFInfo
- Publication number
- ZA200300250B ZA200300250B ZA200300250A ZA200300250A ZA200300250B ZA 200300250 B ZA200300250 B ZA 200300250B ZA 200300250 A ZA200300250 A ZA 200300250A ZA 200300250 A ZA200300250 A ZA 200300250A ZA 200300250 B ZA200300250 B ZA 200300250B
- Authority
- ZA
- South Africa
- Prior art keywords
- hair
- group
- acid
- pack
- salt
- Prior art date
Links
- 238000000034 method Methods 0.000 title claims description 48
- 150000003839 salts Chemical class 0.000 claims description 48
- 150000007524 organic acids Chemical class 0.000 claims description 38
- 229910052799 carbon Inorganic materials 0.000 claims description 26
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims description 25
- 239000000203 mixture Substances 0.000 claims description 24
- -1 sulfate ester group Chemical group 0.000 claims description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 13
- 125000001165 hydrophobic group Chemical group 0.000 claims description 12
- 239000000872 buffer Substances 0.000 claims description 11
- 102000011782 Keratins Human genes 0.000 claims description 10
- 108010076876 Keratins Proteins 0.000 claims description 10
- 125000000020 sulfo group Chemical group O=S(=O)([*])O[H] 0.000 claims description 10
- 125000003118 aryl group Chemical group 0.000 claims description 9
- 239000003638 chemical reducing agent Substances 0.000 claims description 9
- 239000007800 oxidant agent Substances 0.000 claims description 9
- 239000006172 buffering agent Substances 0.000 claims description 7
- 230000002378 acidificating effect Effects 0.000 claims description 6
- 238000001035 drying Methods 0.000 claims description 6
- 150000001875 compounds Chemical class 0.000 claims description 5
- 238000010438 heat treatment Methods 0.000 claims description 5
- 125000001476 phosphono group Chemical group [H]OP(*)(=O)O[H] 0.000 claims description 5
- 238000007493 shaping process Methods 0.000 claims description 5
- 229910019142 PO4 Inorganic materials 0.000 claims description 4
- 239000010452 phosphate Substances 0.000 claims description 4
- 125000000213 sulfino group Chemical group [H]OS(*)=O 0.000 claims description 4
- 230000000694 effects Effects 0.000 description 16
- 239000002253 acid Substances 0.000 description 15
- 125000001183 hydrocarbyl group Chemical group 0.000 description 10
- 125000001931 aliphatic group Chemical group 0.000 description 9
- 125000004432 carbon atom Chemical group C* 0.000 description 9
- 125000003545 alkoxy group Chemical group 0.000 description 8
- 125000002723 alicyclic group Chemical group 0.000 description 7
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229920006395 saturated elastomer Polymers 0.000 description 6
- 150000007513 acids Chemical class 0.000 description 5
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 description 4
- 125000006615 aromatic heterocyclic group Chemical group 0.000 description 4
- 125000000623 heterocyclic group Chemical group 0.000 description 4
- 239000007864 aqueous solution Substances 0.000 description 3
- 125000002029 aromatic hydrocarbon group Chemical group 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
- 238000010409 ironing Methods 0.000 description 3
- 150000003460 sulfonic acids Chemical class 0.000 description 3
- AEMRFAOFKBGASW-UHFFFAOYSA-N Glycolic acid Chemical compound OCC(O)=O AEMRFAOFKBGASW-UHFFFAOYSA-N 0.000 description 2
- 150000003863 ammonium salts Chemical class 0.000 description 2
- 239000002585 base Substances 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid Chemical compound OC(=O)C1=CC=CC=C1 WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 238000010494 dissociation reaction Methods 0.000 description 2
- 230000005593 dissociations Effects 0.000 description 2
- 229910052742 iron Inorganic materials 0.000 description 2
- 125000005956 isoquinolyl group Chemical group 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 125000001624 naphthyl group Chemical group 0.000 description 2
- 235000005985 organic acids Nutrition 0.000 description 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 2
- 159000000000 sodium salts Chemical class 0.000 description 2
- JIRHAGAOHOYLNO-UHFFFAOYSA-N (3-cyclopentyloxy-4-methoxyphenyl)methanol Chemical compound COC1=CC=C(CO)C=C1OC1CCCC1 JIRHAGAOHOYLNO-UHFFFAOYSA-N 0.000 description 1
- MIOPJNTWMNEORI-GMSGAONNSA-N (S)-camphorsulfonic acid Chemical compound C1C[C@@]2(CS(O)(=O)=O)C(=O)C[C@@H]1C2(C)C MIOPJNTWMNEORI-GMSGAONNSA-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
- FDVWKHPUNHWEJY-BQYQJAHWSA-N (e)-oct-1-ene-1-sulfonic acid Chemical compound CCCCCC\C=C\S(O)(=O)=O FDVWKHPUNHWEJY-BQYQJAHWSA-N 0.000 description 1
- BEJNTOQZNHFUFT-UHFFFAOYSA-N 1-ethylcyclohexane-1-sulfonic acid Chemical compound CCC1(S(O)(=O)=O)CCCCC1 BEJNTOQZNHFUFT-UHFFFAOYSA-N 0.000 description 1
- CDJSTTLHXKMUHW-UHFFFAOYSA-N 1-methylcyclohexane-1-sulfonic acid Chemical compound OS(=O)(=O)C1(C)CCCCC1 CDJSTTLHXKMUHW-UHFFFAOYSA-N 0.000 description 1
- IXWAKAUODNZTFC-UHFFFAOYSA-N 1-phenoxyethanesulfonic acid Chemical compound OS(=O)(=O)C(C)OC1=CC=CC=C1 IXWAKAUODNZTFC-UHFFFAOYSA-N 0.000 description 1
- COFMBBYARPOGBA-UHFFFAOYSA-N 1-phenylethanesulfonic acid Chemical compound OS(=O)(=O)C(C)C1=CC=CC=C1 COFMBBYARPOGBA-UHFFFAOYSA-N 0.000 description 1
- BASAOTXPYDXFSX-UHFFFAOYSA-N 1-phenylhex-1-ene-2-sulfonic acid Chemical compound CCCCC(S(O)(=O)=O)=CC1=CC=CC=C1 BASAOTXPYDXFSX-UHFFFAOYSA-N 0.000 description 1
- VROHJEGFIJETEV-UHFFFAOYSA-N 1-phenylpentane-1-sulfonic acid Chemical compound CCCCC(S(O)(=O)=O)C1=CC=CC=C1 VROHJEGFIJETEV-UHFFFAOYSA-N 0.000 description 1
- UCWYIXXOGZQXSN-UHFFFAOYSA-N 1-phenylprop-1-ene-2-sulfonic acid Chemical compound OS(=O)(=O)C(C)=CC1=CC=CC=C1 UCWYIXXOGZQXSN-UHFFFAOYSA-N 0.000 description 1
- XWIAHIXALOBXNK-UHFFFAOYSA-N 1-phenylpropane-1-sulfonic acid Chemical compound CCC(S(O)(=O)=O)C1=CC=CC=C1 XWIAHIXALOBXNK-UHFFFAOYSA-N 0.000 description 1
- JITXLTLNJIRPBR-UHFFFAOYSA-N 1-tert-butylcyclohexane-1-sulfonic acid Chemical compound CC(C)(C)C1(S(O)(=O)=O)CCCCC1 JITXLTLNJIRPBR-UHFFFAOYSA-N 0.000 description 1
- FDYKGJFSAUBIOO-UHFFFAOYSA-N 1h-indene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)C=CC2=C1 FDYKGJFSAUBIOO-UHFFFAOYSA-N 0.000 description 1
- XNJVIJQATFJERB-UHFFFAOYSA-N 2,3,4-trimethylbenzenesulfonic acid Chemical compound CC1=CC=C(S(O)(=O)=O)C(C)=C1C XNJVIJQATFJERB-UHFFFAOYSA-N 0.000 description 1
- QWFMDSOYEQHWMF-UHFFFAOYSA-N 2,3-bis(ethenyl)benzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC(C=C)=C1C=C QWFMDSOYEQHWMF-UHFFFAOYSA-N 0.000 description 1
- UFTUYFPADJIUDL-UHFFFAOYSA-N 2,3-diethylbenzenesulfonic acid Chemical compound CCC1=CC=CC(S(O)(=O)=O)=C1CC UFTUYFPADJIUDL-UHFFFAOYSA-N 0.000 description 1
- SDRWSOSZWGTKEF-UHFFFAOYSA-N 2,3-dimethylnaphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(O)(=O)=O)=C(C)C(C)=CC2=C1 SDRWSOSZWGTKEF-UHFFFAOYSA-N 0.000 description 1
- RSZWQKFPYYKZBJ-UHFFFAOYSA-N 2,3-ditert-butylbenzenesulfonic acid Chemical compound CC(C)(C)C1=CC=CC(S(O)(=O)=O)=C1C(C)(C)C RSZWQKFPYYKZBJ-UHFFFAOYSA-N 0.000 description 1
- LBLYYCQCTBFVLH-UHFFFAOYSA-N 2-Methylbenzenesulfonic acid Chemical compound CC1=CC=CC=C1S(O)(=O)=O LBLYYCQCTBFVLH-UHFFFAOYSA-N 0.000 description 1
- GOJUJUVQIVIZAV-UHFFFAOYSA-N 2-amino-4,6-dichloropyrimidine-5-carbaldehyde Chemical group NC1=NC(Cl)=C(C=O)C(Cl)=N1 GOJUJUVQIVIZAV-UHFFFAOYSA-N 0.000 description 1
- BFIHAWRLMJFWHG-UHFFFAOYSA-N 2-butan-2-ylbenzenesulfonic acid Chemical compound CCC(C)C1=CC=CC=C1S(O)(=O)=O BFIHAWRLMJFWHG-UHFFFAOYSA-N 0.000 description 1
- QZIFXWQGNHGNQV-UHFFFAOYSA-N 2-butyl-3-methylbenzenesulfonic acid Chemical compound CCCCC1=C(C)C=CC=C1S(O)(=O)=O QZIFXWQGNHGNQV-UHFFFAOYSA-N 0.000 description 1
- SWDHKZPAUHBMHV-UHFFFAOYSA-N 2-ethoxybenzenesulfonic acid Chemical compound CCOC1=CC=CC=C1S(O)(=O)=O SWDHKZPAUHBMHV-UHFFFAOYSA-N 0.000 description 1
- JCRMBLKUFLUWPU-UHFFFAOYSA-N 2-ethylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(CC)=CC=C21 JCRMBLKUFLUWPU-UHFFFAOYSA-N 0.000 description 1
- KBJIFNYHXCIZED-UHFFFAOYSA-N 2-methyl-6-propan-2-ylbenzenesulfonic acid Chemical compound CC(C)C1=CC=CC(C)=C1S(O)(=O)=O KBJIFNYHXCIZED-UHFFFAOYSA-N 0.000 description 1
- WODGMMJHSAKKNF-UHFFFAOYSA-N 2-methylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(C)=CC=C21 WODGMMJHSAKKNF-UHFFFAOYSA-N 0.000 description 1
- QXQNFMNABAJDBZ-UHFFFAOYSA-N 2-methylnonane-2-sulfonic acid Chemical compound CCCCCCCC(C)(C)S(O)(=O)=O QXQNFMNABAJDBZ-UHFFFAOYSA-N 0.000 description 1
- SYYFUZIORIDIML-UHFFFAOYSA-N 2-methyloctane-2-sulfonic acid Chemical compound CCCCCCC(C)(C)S(O)(=O)=O SYYFUZIORIDIML-UHFFFAOYSA-N 0.000 description 1
- QSFUHVVPRDXERQ-UHFFFAOYSA-N 2-methylpentane-2-sulfonic acid Chemical compound CCCC(C)(C)S(O)(=O)=O QSFUHVVPRDXERQ-UHFFFAOYSA-N 0.000 description 1
- WRZDSZXJYGDDBE-UHFFFAOYSA-N 2-phenoxybenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1OC1=CC=CC=C1 WRZDSZXJYGDDBE-UHFFFAOYSA-N 0.000 description 1
- RIOSJKSGNLGONI-UHFFFAOYSA-N 2-phenylbenzenesulfonic acid Chemical compound OS(=O)(=O)C1=CC=CC=C1C1=CC=CC=C1 RIOSJKSGNLGONI-UHFFFAOYSA-N 0.000 description 1
- AGBXYHCHUYARJY-UHFFFAOYSA-N 2-phenylethenesulfonic acid Chemical compound OS(=O)(=O)C=CC1=CC=CC=C1 AGBXYHCHUYARJY-UHFFFAOYSA-N 0.000 description 1
- JBVOQKNLGSOPNZ-UHFFFAOYSA-N 2-propan-2-ylbenzenesulfonic acid Chemical compound CC(C)C1=CC=CC=C1S(O)(=O)=O JBVOQKNLGSOPNZ-UHFFFAOYSA-N 0.000 description 1
- ZTFYJIXFKGPCHV-UHFFFAOYSA-N 2-propan-2-ylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=C(S(O)(=O)=O)C(C(C)C)=CC=C21 ZTFYJIXFKGPCHV-UHFFFAOYSA-N 0.000 description 1
- FWMKPJYJDJSEHR-UHFFFAOYSA-N 2-propylnaphthalene-1-sulfonic acid Chemical group C1=CC=CC2=C(S(O)(=O)=O)C(CCC)=CC=C21 FWMKPJYJDJSEHR-UHFFFAOYSA-N 0.000 description 1
- LNUMHIKQPHWQFR-UHFFFAOYSA-N 3-butan-2-ylnaphthalene-1-sulfonic acid Chemical compound C1=CC=CC2=CC(C(C)CC)=CC(S(O)(=O)=O)=C21 LNUMHIKQPHWQFR-UHFFFAOYSA-N 0.000 description 1
- OMUXQEBSSIZFAX-UHFFFAOYSA-N 3-methylnona-2,4-diene-2-sulfonic acid Chemical compound CCCCC=CC(C)=C(C)S(O)(=O)=O OMUXQEBSSIZFAX-UHFFFAOYSA-N 0.000 description 1
- ZFXSPWNRECCHIG-UHFFFAOYSA-N 3-methylpent-1-yne-1-sulfonic acid Chemical compound CCC(C)C#CS(O)(=O)=O ZFXSPWNRECCHIG-UHFFFAOYSA-N 0.000 description 1
- OPUILGVLAQHFHX-UHFFFAOYSA-N 3-methylquinoline-2-sulfonic acid Chemical compound C1=CC=C2N=C(S(O)(=O)=O)C(C)=CC2=C1 OPUILGVLAQHFHX-UHFFFAOYSA-N 0.000 description 1
- MLXVOLMICGGEPZ-UHFFFAOYSA-N 4,4-dimethylcyclohexane-1-sulfonic acid Chemical compound CC1(CCC(CC1)S(=O)(=O)O)C MLXVOLMICGGEPZ-UHFFFAOYSA-N 0.000 description 1
- CVLHGLWXLDOELD-UHFFFAOYSA-N 4-(Propan-2-yl)benzenesulfonic acid Chemical compound CC(C)C1=CC=C(S(O)(=O)=O)C=C1 CVLHGLWXLDOELD-UHFFFAOYSA-N 0.000 description 1
- BRIXOPDYGQCZFO-UHFFFAOYSA-N 4-ethylphenylsulfonic acid Chemical compound CCC1=CC=C(S(O)(=O)=O)C=C1 BRIXOPDYGQCZFO-UHFFFAOYSA-N 0.000 description 1
- JNQGABCUYOQESU-UHFFFAOYSA-N 5,5-dimethylhex-1-ene-1-sulfonic acid Chemical compound CC(C)(C)CCC=CS(O)(=O)=O JNQGABCUYOQESU-UHFFFAOYSA-N 0.000 description 1
- ZFHXNMJGZBQGTO-UHFFFAOYSA-N 5,5-dimethylhexane-1-sulfonic acid Chemical compound CC(C)(C)CCCCS(O)(=O)=O ZFHXNMJGZBQGTO-UHFFFAOYSA-N 0.000 description 1
- ODHCTXKNWHHXJC-VKHMYHEASA-N 5-oxo-L-proline Chemical compound OC(=O)[C@@H]1CCC(=O)N1 ODHCTXKNWHHXJC-VKHMYHEASA-N 0.000 description 1
- CXPPJTXSXODHOD-UHFFFAOYSA-N 6,6-dimethylheptane-1-sulfonic acid Chemical compound CC(C)(C)CCCCCS(O)(=O)=O CXPPJTXSXODHOD-UHFFFAOYSA-N 0.000 description 1
- SCGORAJGRKNBSY-UHFFFAOYSA-N 9h-fluorene-1-sulfonic acid Chemical compound C1C2=CC=CC=C2C2=C1C(S(=O)(=O)O)=CC=C2 SCGORAJGRKNBSY-UHFFFAOYSA-N 0.000 description 1
- 239000005711 Benzoic acid Substances 0.000 description 1
- HYBYNIAISJOVHP-UHFFFAOYSA-N CC(C=CC=CC=CS(=O)(=O)O)(C)C Chemical compound CC(C=CC=CC=CS(=O)(=O)O)(C)C HYBYNIAISJOVHP-UHFFFAOYSA-N 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
- 229910004727 OSO3H Inorganic materials 0.000 description 1
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-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
- 229910052783 alkali metal Inorganic materials 0.000 description 1
- 229910052784 alkaline earth metal Inorganic materials 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
- ILFFFKFZHRGICY-UHFFFAOYSA-N anthracene-1-sulfonic acid Chemical compound C1=CC=C2C=C3C(S(=O)(=O)O)=CC=CC3=CC2=C1 ILFFFKFZHRGICY-UHFFFAOYSA-N 0.000 description 1
- 125000005428 anthryl group Chemical group [H]C1=C([H])C([H])=C2C([H])=C3C(*)=C([H])C([H])=C([H])C3=C([H])C2=C1[H] 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 235000010233 benzoic acid Nutrition 0.000 description 1
- KDYFGRWQOYBRFD-NUQCWPJISA-N butanedioic acid Chemical compound O[14C](=O)CC[14C](O)=O KDYFGRWQOYBRFD-NUQCWPJISA-N 0.000 description 1
- 125000002843 carboxylic acid group Chemical group 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- 125000001485 cycloalkadienyl group Chemical group 0.000 description 1
- 125000002772 cycloalkatrienyl group Chemical group 0.000 description 1
- 125000000392 cycloalkenyl group Chemical group 0.000 description 1
- 125000000753 cycloalkyl group Chemical group 0.000 description 1
- ZHGASCUQXLPSDT-UHFFFAOYSA-N cyclohexanesulfonic acid Chemical compound OS(=O)(=O)C1CCCCC1 ZHGASCUQXLPSDT-UHFFFAOYSA-N 0.000 description 1
- BAYVBPQZKYSHDL-UHFFFAOYSA-N cyclohexene-1-sulfonic acid Chemical compound OS(=O)(=O)C1=CCCCC1 BAYVBPQZKYSHDL-UHFFFAOYSA-N 0.000 description 1
- MQEHNPJPYKSQBY-UHFFFAOYSA-N diphenylmethanesulfonic acid Chemical compound C=1C=CC=CC=1C(S(=O)(=O)O)C1=CC=CC=C1 MQEHNPJPYKSQBY-UHFFFAOYSA-N 0.000 description 1
- 125000005982 diphenylmethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])(*)C1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 description 1
- 125000003983 fluorenyl group Chemical group C1(=CC=CC=2C3=CC=CC=C3CC12)* 0.000 description 1
- 125000002541 furyl group Chemical group 0.000 description 1
- 230000003806 hair structure Effects 0.000 description 1
- OATNUSMUMWYMJP-UHFFFAOYSA-N hept-1-ene-1-sulfonic acid Chemical compound CCCCCC=CS(O)(=O)=O OATNUSMUMWYMJP-UHFFFAOYSA-N 0.000 description 1
- AKRQHOWXVSDJEF-UHFFFAOYSA-N heptane-1-sulfonic acid Chemical group CCCCCCCS(O)(=O)=O AKRQHOWXVSDJEF-UHFFFAOYSA-N 0.000 description 1
- VFIJKQJHCCRWHE-UHFFFAOYSA-N hex-1-ene-1-sulfonic acid Chemical compound CCCCC=CS(O)(=O)=O VFIJKQJHCCRWHE-UHFFFAOYSA-N 0.000 description 1
- FYAQQULBLMNGAH-UHFFFAOYSA-N hexane-1-sulfonic acid Chemical group CCCCCCS(O)(=O)=O FYAQQULBLMNGAH-UHFFFAOYSA-N 0.000 description 1
- WAASCVGPJBHARY-UHFFFAOYSA-N hexane-2-sulfonic acid Chemical compound CCCCC(C)S(O)(=O)=O WAASCVGPJBHARY-UHFFFAOYSA-N 0.000 description 1
- OOZYQDUFRNYGBN-UHFFFAOYSA-N hexane-3-sulfonic acid Chemical compound CCCC(CC)S(O)(=O)=O OOZYQDUFRNYGBN-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- 125000003454 indenyl group Chemical group C1(C=CC2=CC=CC=C12)* 0.000 description 1
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
- USPHIQNVSKCZDF-UHFFFAOYSA-N isoquinoline-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=NC=CC2=C1 USPHIQNVSKCZDF-UHFFFAOYSA-N 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 238000012423 maintenance Methods 0.000 description 1
- 239000001630 malic acid Substances 0.000 description 1
- 235000011090 malic acid Nutrition 0.000 description 1
- 150000007522 mineralic acids Chemical class 0.000 description 1
- 125000004573 morpholin-4-yl group Chemical group N1(CCOCC1)* 0.000 description 1
- 125000002757 morpholinyl group Chemical group 0.000 description 1
- PSZYNBSKGUBXEH-UHFFFAOYSA-N naphthalene-1-sulfonic acid Chemical compound C1=CC=C2C(S(=O)(=O)O)=CC=CC2=C1 PSZYNBSKGUBXEH-UHFFFAOYSA-N 0.000 description 1
- WLGDAKIJYPIYLR-UHFFFAOYSA-N octane-1-sulfonic acid Chemical group CCCCCCCCS(O)(=O)=O WLGDAKIJYPIYLR-UHFFFAOYSA-N 0.000 description 1
- KMIGUAKLWIAHTQ-UHFFFAOYSA-N octane-3-sulfonic acid Chemical compound CCCCCC(CC)S(O)(=O)=O KMIGUAKLWIAHTQ-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 150000003014 phosphoric acid esters Chemical class 0.000 description 1
- 150000003016 phosphoric acids Chemical class 0.000 description 1
- 125000000587 piperidin-1-yl group Chemical group [H]C1([H])N(*)C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000005936 piperidyl group Chemical group 0.000 description 1
- XAEFZNCEHLXOMS-UHFFFAOYSA-M potassium benzoate Chemical compound [K+].[O-]C(=O)C1=CC=CC=C1 XAEFZNCEHLXOMS-UHFFFAOYSA-M 0.000 description 1
- 159000000001 potassium salts Chemical class 0.000 description 1
- 230000001737 promoting effect Effects 0.000 description 1
- 229940079889 pyrrolidonecarboxylic acid Drugs 0.000 description 1
- 125000000168 pyrrolyl group Chemical group 0.000 description 1
- ZKIHLVYBGPFUAD-UHFFFAOYSA-N quinoline-2-sulfonic acid Chemical compound C1=CC=CC2=NC(S(=O)(=O)O)=CC=C21 ZKIHLVYBGPFUAD-UHFFFAOYSA-N 0.000 description 1
- 125000005493 quinolyl group Chemical group 0.000 description 1
- 238000006894 reductive elimination reaction Methods 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 125000000542 sulfonic acid group Chemical group 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 125000001544 thienyl group Chemical group 0.000 description 1
- 238000005406 washing 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
- A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
- A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
-
- 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
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/04—Preparations for permanent waving or straightening the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/24—Thermal properties
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/52—Stabilizers
-
- 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
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP2001168078A JP3703738B2 (ja) | 2001-06-04 | 2001-06-04 | 縮毛矯正方法 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ZA200300250B true ZA200300250B (en) | 2004-02-10 |
Family
ID=19010362
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ZA200300250A ZA200300250B (en) | 2001-06-04 | 2003-01-09 | Method of treating hair. |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20040011373A1 (ja) |
| EP (1) | EP1393708B1 (ja) |
| JP (1) | JP3703738B2 (ja) |
| KR (1) | KR20030020961A (ja) |
| CN (1) | CN1253143C (ja) |
| BR (1) | BR0205514B1 (ja) |
| ES (1) | ES2504316T3 (ja) |
| MX (1) | MXPA03001032A (ja) |
| TW (1) | TWI311487B (ja) |
| WO (1) | WO2002098381A1 (ja) |
| ZA (1) | ZA200300250B (ja) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| KR100389706B1 (en) * | 2003-02-10 | 2003-06-28 | Beebong Fine Ltd | Composition of self-diagnosis and reduction catalyst type permanent and straightener and manufacturing method thereof |
| JP4589820B2 (ja) * | 2005-06-20 | 2010-12-01 | 花王株式会社 | 毛髪化粧料 |
| JP4931374B2 (ja) * | 2005-06-20 | 2012-05-16 | 花王株式会社 | 毛髪化粧料 |
| FR2901471B1 (fr) | 2006-05-24 | 2010-06-04 | Oreal | Procede de defrisage des fibres keratiniques avec un moyen de chauffage et un derive d'acide |
| DE102008062397A1 (de) * | 2008-12-17 | 2010-06-24 | Henkel Ag & Co. Kgaa | Farbabzug mit Wärmebehandlung |
| CN102008424B (zh) * | 2010-12-17 | 2012-05-23 | 广州温雅日用化妆品有限公司 | 凝露状直发剂 |
| DE102010064052A1 (de) * | 2010-12-23 | 2012-06-28 | Henkel Ag & Co. Kgaa | Verfahren zur Umformung keratinhaltiger Fasern |
| EP2852375B1 (en) | 2012-05-21 | 2018-04-04 | Unilever PLC | Method of treating hair |
| US9572761B2 (en) | 2012-05-21 | 2017-02-21 | Conopco, Inc. | Method of treating hair |
| WO2013174703A1 (en) | 2012-05-21 | 2013-11-28 | Unilever Plc | Method of treating hair |
| FR3009681B1 (fr) * | 2013-08-13 | 2015-08-07 | Oreal | Procede de traitement des fibres keratiniques a partir d'une composition hydroalcoolique comprenant un mono acide organique |
| US10588839B2 (en) | 2013-11-21 | 2020-03-17 | Conopco, Inc. | Method of shaping hair |
| JP6707449B2 (ja) | 2013-11-21 | 2020-06-10 | ユニリーバー・ナームローゼ・ベンノートシヤープ | 毛髪の処理方法 |
| EP3082731B1 (en) | 2013-12-19 | 2018-07-04 | The Procter and Gamble Company | Shaping keratin fibres using an active agent comprising at least two functional groups selected from: -c(oh)- and -c(=o)oh |
| JP2016540006A (ja) | 2013-12-19 | 2016-12-22 | ザ プロクター アンド ギャンブル カンパニー | 還元性組成物及び定着用組成物を使用したケラチン繊維の整形 |
| EP3082736B1 (en) | 2013-12-19 | 2018-08-08 | The Procter and Gamble Company | Shaping keratin fibres using 2-hydroxypropane-1,2,3-tricarboxylic acid and/or 1,2,3,4-butanetetracarboxylic acid |
| CN105828786B (zh) | 2013-12-19 | 2020-07-07 | 宝洁公司 | 使用包含选自-c(＝o)-、-c(＝o)-h和-c(＝o)-o-的官能团的an活性剂使角蛋白纤维成形 |
| JP6314235B2 (ja) | 2013-12-19 | 2018-04-18 | ザ プロクター アンド ギャンブル カンパニー | オキソエタン酸及び／又はその誘導体を使用したヒトの毛髪をまっすぐにする方法 |
| EP3082747B1 (en) | 2013-12-19 | 2018-07-04 | The Procter and Gamble Company | Shaping keratin fibres using a sugar |
| EP3082744A1 (en) | 2013-12-19 | 2016-10-26 | The Procter & Gamble Company | Shaping keratin fibres using carbonate ester |
| EP3297730A1 (en) | 2014-12-19 | 2018-03-28 | The Procter and Gamble Company | Method of shaping keratin fibres |
| EP3297731A1 (en) | 2014-12-19 | 2018-03-28 | The Procter and Gamble Company | Shaping keratin fibres using arabinose and ethylene carbonate |
| WO2016205580A1 (en) | 2015-06-18 | 2016-12-22 | The Procter & Gamble Company | Shaping keratin fibres using dialdehyde compounds |
| CN108366943B (zh) * | 2015-12-25 | 2022-01-25 | 花王株式会社 | 毛发处理方法 |
| JP6524334B2 (ja) * | 2016-03-09 | 2019-06-05 | 昌代 熊谷 | 毛髪処理方法及び毛髪処理剤セット |
| BR112019015773B1 (pt) * | 2017-01-31 | 2022-07-12 | Kao Corporation | Método de tratamento capilar |
| JP7094661B2 (ja) * | 2017-04-24 | 2022-07-04 | 花王株式会社 | 毛髪処理方法 |
| JP7458207B2 (ja) * | 2019-05-10 | 2024-03-29 | 花王株式会社 | 毛髪処理方法 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB690866A (en) * | 1949-02-15 | 1953-04-29 | Henkel & Cie Gmbh | Process for the permanent waving of hair or equivalent operation |
| US3482581A (en) * | 1966-08-01 | 1969-12-09 | John D Weigand | Straightening of live human hair with an aqueous acidic glycol solution |
| JPS58222008A (ja) * | 1982-06-16 | 1983-12-23 | Lion Corp | パ−マネントウエ−ブ剤 |
| US5240695A (en) * | 1988-02-11 | 1993-08-31 | L'oreal | Use of 2-hydroxy-4-methoxybenzophenone-5-sulphonic acid or its salts for protecting the hair against environmental attacking agents, and especially against light and process for protecting the hair using the compound |
| EP0529437B1 (en) * | 1991-08-14 | 1996-07-17 | Kao Corporation | Hair treatment composition |
| JP2562405B2 (ja) * | 1993-04-06 | 1996-12-11 | 花王株式会社 | ケラチン繊維処理剤組成物 |
| JP2562407B2 (ja) * | 1993-04-28 | 1996-12-11 | 花王株式会社 | ケラチン繊維処理剤 |
| JPH07101840A (ja) * | 1993-10-06 | 1995-04-18 | Kao Corp | 縮毛矯正剤組成物及び該組成物を用いる縮毛矯正方法 |
| JP3190792B2 (ja) * | 1994-09-29 | 2001-07-23 | 花王株式会社 | 毛髪変形剤組成物 |
-
2001
- 2001-06-04 JP JP2001168078A patent/JP3703738B2/ja not_active Expired - Fee Related
-
2002
- 2002-06-03 BR BRPI0205514-7B1A patent/BR0205514B1/pt not_active IP Right Cessation
- 2002-06-03 EP EP02730869.1A patent/EP1393708B1/en not_active Expired - Lifetime
- 2002-06-03 CN CNB028018265A patent/CN1253143C/zh not_active Expired - Fee Related
- 2002-06-03 MX MXPA03001032A patent/MXPA03001032A/es unknown
- 2002-06-03 KR KR10-2003-7001534A patent/KR20030020961A/ko not_active Application Discontinuation
- 2002-06-03 ES ES02730869.1T patent/ES2504316T3/es not_active Expired - Lifetime
- 2002-06-03 US US10/333,914 patent/US20040011373A1/en not_active Abandoned
- 2002-06-03 WO PCT/JP2002/005419 patent/WO2002098381A1/ja active Application Filing
- 2002-06-04 TW TW091111972A patent/TWI311487B/zh not_active IP Right Cessation
-
2003
- 2003-01-09 ZA ZA200300250A patent/ZA200300250B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002363042A (ja) | 2002-12-18 |
| KR20030020961A (ko) | 2003-03-10 |
| EP1393708A1 (en) | 2004-03-03 |
| TWI311487B (ja) | 2009-07-01 |
| EP1393708B1 (en) | 2014-07-02 |
| CN1253143C (zh) | 2006-04-26 |
| CN1463190A (zh) | 2003-12-24 |
| MXPA03001032A (es) | 2004-09-10 |
| WO2002098381A1 (fr) | 2002-12-12 |
| JP3703738B2 (ja) | 2005-10-05 |
| US20040011373A1 (en) | 2004-01-22 |
| BR0205514A (pt) | 2003-07-08 |
| BR0205514B1 (pt) | 2013-10-01 |
| ES2504316T3 (es) | 2014-10-08 |
| EP1393708A4 (en) | 2010-02-17 |
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