WO2004098488A2 - Utilisation de dithiols dans une composition de deformation permanente des cheveux - Google Patents
Utilisation de dithiols dans une composition de deformation permanente des cheveux Download PDFInfo
- Publication number
- WO2004098488A2 WO2004098488A2 PCT/FR2004/001071 FR2004001071W WO2004098488A2 WO 2004098488 A2 WO2004098488 A2 WO 2004098488A2 FR 2004001071 W FR2004001071 W FR 2004001071W WO 2004098488 A2 WO2004098488 A2 WO 2004098488A2
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- formula
- composition
- hair
- reducing
- radical
- Prior art date
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 77
- 150000004662 dithiols Chemical class 0.000 title claims abstract description 25
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- 238000000034 method Methods 0.000 claims abstract description 14
- 239000002537 cosmetic Substances 0.000 claims abstract description 12
- 125000000129 anionic group Chemical group 0.000 claims abstract description 8
- 125000002091 cationic group Chemical group 0.000 claims abstract description 8
- 239000004094 surface-active agent Substances 0.000 claims abstract description 7
- 229920000642 polymer Polymers 0.000 claims abstract description 4
- -1 cyano, ureido groups Chemical group 0.000 claims description 28
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 14
- OAKJQQAXSVQMHS-UHFFFAOYSA-N Hydrazine Chemical compound NN OAKJQQAXSVQMHS-UHFFFAOYSA-N 0.000 claims description 14
- 239000003638 chemical reducing agent Substances 0.000 claims description 14
- 239000003795 chemical substances by application Substances 0.000 claims description 13
- 102000011782 Keratins Human genes 0.000 claims description 12
- 108010076876 Keratins Proteins 0.000 claims description 12
- 150000002148 esters Chemical class 0.000 claims description 10
- 229910052760 oxygen Inorganic materials 0.000 claims description 10
- 229910052717 sulfur Inorganic materials 0.000 claims description 9
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 claims description 8
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims description 8
- 239000000835 fiber Substances 0.000 claims description 8
- WCYWZMWISLQXQU-UHFFFAOYSA-N methyl Chemical compound [CH3] WCYWZMWISLQXQU-UHFFFAOYSA-N 0.000 claims description 8
- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
- 239000001301 oxygen Substances 0.000 claims description 8
- 150000003254 radicals Chemical class 0.000 claims description 8
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 claims description 7
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 7
- XUIMIQQOPSSXEZ-UHFFFAOYSA-N Silicon Chemical compound [Si] XUIMIQQOPSSXEZ-UHFFFAOYSA-N 0.000 claims description 7
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 claims description 7
- 150000001408 amides Chemical class 0.000 claims description 7
- 125000005842 heteroatom Chemical group 0.000 claims description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 7
- 229910052698 phosphorus Inorganic materials 0.000 claims description 7
- 239000011574 phosphorus Substances 0.000 claims description 7
- 229910052710 silicon Inorganic materials 0.000 claims description 7
- 239000010703 silicon Substances 0.000 claims description 7
- 125000001424 substituent group Chemical group 0.000 claims description 7
- 239000011593 sulfur Substances 0.000 claims description 7
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 7
- 239000002253 acid Substances 0.000 claims description 6
- OWIUPIRUAQMTTK-UHFFFAOYSA-N carbazic acid Chemical compound NNC(O)=O OWIUPIRUAQMTTK-UHFFFAOYSA-N 0.000 claims description 5
- 125000001183 hydrocarbyl group Chemical group 0.000 claims description 5
- 150000007513 acids Chemical class 0.000 claims description 4
- 125000004432 carbon atom Chemical group C* 0.000 claims description 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 claims description 4
- 125000004122 cyclic group Chemical group 0.000 claims description 4
- 239000000975 dye Substances 0.000 claims description 4
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 4
- 230000003287 optical effect Effects 0.000 claims description 4
- 150000002170 ethers Chemical class 0.000 claims description 3
- 150000002191 fatty alcohols Chemical class 0.000 claims description 3
- 239000002304 perfume Substances 0.000 claims description 3
- 229920006395 saturated elastomer Polymers 0.000 claims description 3
- 239000002562 thickening agent Substances 0.000 claims description 3
- KXDHJXZQYSOELW-UHFFFAOYSA-M Carbamate Chemical compound NC([O-])=O KXDHJXZQYSOELW-UHFFFAOYSA-M 0.000 claims description 2
- GHOKWGTUZJEAQD-UHFFFAOYSA-N Chick antidermatitis factor Natural products OCC(C)(C)C(O)C(=O)NCCC(O)=O GHOKWGTUZJEAQD-UHFFFAOYSA-N 0.000 claims description 2
- 208000001840 Dandruff Diseases 0.000 claims description 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 2
- 239000004166 Lanolin Chemical class 0.000 claims description 2
- 239000004480 active ingredient Substances 0.000 claims description 2
- 239000000654 additive Substances 0.000 claims description 2
- 125000003277 amino group Chemical group 0.000 claims description 2
- 239000001257 hydrogen Substances 0.000 claims description 2
- 229910052739 hydrogen Inorganic materials 0.000 claims description 2
- 229940039717 lanolin Drugs 0.000 claims description 2
- 235000019388 lanolin Nutrition 0.000 claims description 2
- 235000019161 pantothenic acid Nutrition 0.000 claims description 2
- 239000011713 pantothenic acid Substances 0.000 claims description 2
- 239000003755 preservative agent Substances 0.000 claims description 2
- 239000003352 sequestering agent Substances 0.000 claims description 2
- 230000000475 sunscreen effect Effects 0.000 claims description 2
- 239000000516 sunscreening agent Substances 0.000 claims description 2
- 239000000375 suspending agent Substances 0.000 claims description 2
- 230000000996 additive effect Effects 0.000 claims 1
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 12
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 8
- 230000001590 oxidative effect Effects 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- 239000003513 alkali Substances 0.000 description 5
- 239000006210 lotion Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 4
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 4
- 230000015556 catabolic process Effects 0.000 description 4
- 239000006071 cream Substances 0.000 description 4
- 235000018417 cysteine Nutrition 0.000 description 4
- XUJNEKJLAYXESH-UHFFFAOYSA-N cysteine Natural products SCC(N)C(O)=O XUJNEKJLAYXESH-UHFFFAOYSA-N 0.000 description 4
- 238000006731 degradation reaction Methods 0.000 description 4
- 235000013870 dimethyl polysiloxane Nutrition 0.000 description 4
- 230000003647 oxidation Effects 0.000 description 4
- 238000007254 oxidation reaction Methods 0.000 description 4
- YWXCBLUCVBSYNJ-UHFFFAOYSA-N 2-(2-sulfanylethylsulfonyl)ethanethiol Chemical compound SCCS(=O)(=O)CCS YWXCBLUCVBSYNJ-UHFFFAOYSA-N 0.000 description 3
- QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-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
- SXDBWCPKPHAZSM-UHFFFAOYSA-M bromate Inorganic materials [O-]Br(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-M 0.000 description 3
- SXDBWCPKPHAZSM-UHFFFAOYSA-N bromic acid Chemical compound OBr(=O)=O SXDBWCPKPHAZSM-UHFFFAOYSA-N 0.000 description 3
- 239000004205 dimethyl polysiloxane Substances 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 3
- 150000003839 salts Chemical class 0.000 description 3
- LTMQZVLXCLQPCT-UHFFFAOYSA-N 1,1,6-trimethyltetralin Chemical compound C1CCC(C)(C)C=2C1=CC(C)=CC=2 LTMQZVLXCLQPCT-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
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 2
- VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 2
- XUJNEKJLAYXESH-REOHCLBHSA-N L-Cysteine Chemical compound SC[C@H](N)C(O)=O XUJNEKJLAYXESH-REOHCLBHSA-N 0.000 description 2
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 229910052784 alkaline earth metal Inorganic materials 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 239000001099 ammonium carbonate Substances 0.000 description 2
- 229920006317 cationic polymer Polymers 0.000 description 2
- 235000014113 dietary fatty acids Nutrition 0.000 description 2
- VHJLVAABSRFDPM-QWWZWVQMSA-N dithiothreitol Chemical compound SC[C@@H](O)[C@H](O)CS VHJLVAABSRFDPM-QWWZWVQMSA-N 0.000 description 2
- 229930195729 fatty acid Natural products 0.000 description 2
- 239000000194 fatty acid Substances 0.000 description 2
- 150000004665 fatty acids Chemical class 0.000 description 2
- DOGJSOZYUGJVKS-UHFFFAOYSA-N glyceryl monothioglycolate Chemical compound OCC(O)COC(=O)CS DOGJSOZYUGJVKS-UHFFFAOYSA-N 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N lactic acid Chemical compound CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 125000005358 mercaptoalkyl group Chemical group 0.000 description 2
- PJUIMOJAAPLTRJ-UHFFFAOYSA-N monothioglycerol Chemical compound OCC(O)CS PJUIMOJAAPLTRJ-UHFFFAOYSA-N 0.000 description 2
- 235000019645 odor Nutrition 0.000 description 2
- 229920001296 polysiloxane Polymers 0.000 description 2
- 229940035024 thioglycerol Drugs 0.000 description 2
- XFNJVJPLKCPIBV-UHFFFAOYSA-N trimethylenediamine Chemical compound NCCCN XFNJVJPLKCPIBV-UHFFFAOYSA-N 0.000 description 2
- JCZPMGDSEAFWDY-SQOUGZDYSA-N (2r,3s,4r,5r)-2,3,4,5,6-pentahydroxyhexanamide Chemical compound NC(=O)[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO JCZPMGDSEAFWDY-SQOUGZDYSA-N 0.000 description 1
- TURGQPDWYFJEDY-UHFFFAOYSA-N 1-hydroperoxypropane Chemical compound CCCOO TURGQPDWYFJEDY-UHFFFAOYSA-N 0.000 description 1
- ARXJGSRGQADJSQ-UHFFFAOYSA-N 1-methoxypropan-2-ol Chemical compound COCC(C)O ARXJGSRGQADJSQ-UHFFFAOYSA-N 0.000 description 1
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical compound NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 description 1
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 1
- SKZQZGSPYYHTQG-UHFFFAOYSA-N 4-[2-[4-(3-phenylpyrazolo[1,5-a]pyrimidin-6-yl)phenoxy]ethyl]morpholine Chemical compound C=1C=C(C2=CN3N=CC(=C3N=C2)C=2C=CC=CC=2)C=CC=1OCCN1CCOCC1 SKZQZGSPYYHTQG-UHFFFAOYSA-N 0.000 description 1
- ATRRKUHOCOJYRX-UHFFFAOYSA-N Ammonium bicarbonate Chemical compound [NH4+].OC([O-])=O ATRRKUHOCOJYRX-UHFFFAOYSA-N 0.000 description 1
- 239000004475 Arginine Substances 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- MCBAUZCCHPWCRR-UHFFFAOYSA-N CC(O)C(=S)OCC(O)CO Chemical compound CC(O)C(=S)OCC(O)CO MCBAUZCCHPWCRR-UHFFFAOYSA-N 0.000 description 1
- FNRYGMSRUQRQEY-UHFFFAOYSA-N CN(C(C(CS)=O)O)C(CS)=O Chemical compound CN(C(C(CS)=O)O)C(CS)=O FNRYGMSRUQRQEY-UHFFFAOYSA-N 0.000 description 1
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 1
- WHUUTDBJXJRKMK-UHFFFAOYSA-N Glutamic acid Natural products OC(=O)C(N)CCC(O)=O WHUUTDBJXJRKMK-UHFFFAOYSA-N 0.000 description 1
- PWKSKIMOESPYIA-BYPYZUCNSA-N L-N-acetyl-Cysteine Chemical compound CC(=O)N[C@@H](CS)C(O)=O PWKSKIMOESPYIA-BYPYZUCNSA-N 0.000 description 1
- CKLJMWTZIZZHCS-REOHCLBHSA-N L-aspartic acid Chemical compound OC(=O)[C@@H](N)CC(O)=O CKLJMWTZIZZHCS-REOHCLBHSA-N 0.000 description 1
- LEVWYRKDKASIDU-IMJSIDKUSA-N L-cystine Chemical compound [O-]C(=O)[C@@H]([NH3+])CSSC[C@H]([NH3+])C([O-])=O LEVWYRKDKASIDU-IMJSIDKUSA-N 0.000 description 1
- WHUUTDBJXJRKMK-VKHMYHEASA-N L-glutamic acid Chemical compound OC(=O)[C@@H](N)CCC(O)=O WHUUTDBJXJRKMK-VKHMYHEASA-N 0.000 description 1
- KDXKERNSBIXSRK-UHFFFAOYSA-N Lysine Natural products NCCCCC(N)C(O)=O KDXKERNSBIXSRK-UHFFFAOYSA-N 0.000 description 1
- 239000004472 Lysine Substances 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- AXFZADXWLMXITO-UHFFFAOYSA-N N-acetylcysteamine Chemical compound CC(=O)NCCS AXFZADXWLMXITO-UHFFFAOYSA-N 0.000 description 1
- 206010029216 Nervousness Diseases 0.000 description 1
- 241000208317 Petroselinum Species 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-N Sulfurous acid Chemical class OS(O)=O LSNNMFCWUKXFEE-UHFFFAOYSA-N 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 229960004308 acetylcysteine Drugs 0.000 description 1
- 239000002535 acidifier Substances 0.000 description 1
- 229910001854 alkali hydroxide Inorganic materials 0.000 description 1
- 150000008044 alkali metal hydroxides Chemical class 0.000 description 1
- 150000001342 alkaline earth metals Chemical class 0.000 description 1
- 125000000217 alkyl group Chemical class 0.000 description 1
- 235000001014 amino acid Nutrition 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 235000012538 ammonium bicarbonate Nutrition 0.000 description 1
- 235000012501 ammonium carbonate Nutrition 0.000 description 1
- ZZTCCAPMZLDHFM-UHFFFAOYSA-N ammonium thioglycolate Chemical compound [NH4+].[O-]C(=O)CS ZZTCCAPMZLDHFM-UHFFFAOYSA-N 0.000 description 1
- 229940075861 ammonium thioglycolate Drugs 0.000 description 1
- ODKSFYDXXFIFQN-UHFFFAOYSA-N arginine Natural products OC(=O)C(N)CCCNC(N)=N ODKSFYDXXFIFQN-UHFFFAOYSA-N 0.000 description 1
- 235000003704 aspartic acid Nutrition 0.000 description 1
- OQFSQFPPLPISGP-UHFFFAOYSA-N beta-carboxyaspartic acid Natural products OC(=O)C(N)C(C(O)=O)C(O)=O OQFSQFPPLPISGP-UHFFFAOYSA-N 0.000 description 1
- KGBXLFKZBHKPEV-UHFFFAOYSA-N boric acid Chemical compound OB(O)O KGBXLFKZBHKPEV-UHFFFAOYSA-N 0.000 description 1
- 235000010338 boric acid Nutrition 0.000 description 1
- 239000004327 boric acid Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- STIAPHVBRDNOAJ-UHFFFAOYSA-N carbamimidoylazanium;carbonate Chemical compound NC(N)=N.NC(N)=N.OC(O)=O STIAPHVBRDNOAJ-UHFFFAOYSA-N 0.000 description 1
- 238000005253 cladding Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 238000002788 crimping Methods 0.000 description 1
- UFULAYFCSOUIOV-UHFFFAOYSA-N cysteamine Chemical compound NCCS UFULAYFCSOUIOV-UHFFFAOYSA-N 0.000 description 1
- 229960002433 cysteine Drugs 0.000 description 1
- 229960003067 cystine Drugs 0.000 description 1
- 230000003111 delayed effect Effects 0.000 description 1
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 description 1
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 1
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 239000008387 emulsifying waxe Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 235000002864 food coloring agent Nutrition 0.000 description 1
- 235000013922 glutamic acid Nutrition 0.000 description 1
- 239000004220 glutamic acid Substances 0.000 description 1
- 229940075529 glyceryl stearate Drugs 0.000 description 1
- 229940100242 glycol stearate Drugs 0.000 description 1
- 230000003681 hair reduction Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 235000011167 hydrochloric acid Nutrition 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 239000004310 lactic acid Substances 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229960003151 mercaptamine Drugs 0.000 description 1
- WNZWVZCUFRJIBG-UHFFFAOYSA-N n-(2-sulfanylethyl)propanamide Chemical compound CCC(=O)NCCS WNZWVZCUFRJIBG-UHFFFAOYSA-N 0.000 description 1
- 239000002736 nonionic surfactant Substances 0.000 description 1
- 150000005677 organic carbonates Chemical class 0.000 description 1
- 235000006408 oxalic acid Nutrition 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 230000000149 penetrating effect Effects 0.000 description 1
- 235000011197 perejil Nutrition 0.000 description 1
- 238000005554 pickling Methods 0.000 description 1
- 229920000059 polyethylene glycol stearate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 102000004196 processed proteins & peptides Human genes 0.000 description 1
- 108090000765 processed proteins & peptides Proteins 0.000 description 1
- BDERNNFJNOPAEC-UHFFFAOYSA-N propan-1-ol Chemical compound CCCO BDERNNFJNOPAEC-UHFFFAOYSA-N 0.000 description 1
- 239000003531 protein hydrolysate Substances 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical class 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 238000007493 shaping process Methods 0.000 description 1
- 150000004756 silanes Chemical class 0.000 description 1
- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 235000000346 sugar Nutrition 0.000 description 1
- 150000008163 sugars Chemical class 0.000 description 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 description 1
- LSNNMFCWUKXFEE-UHFFFAOYSA-L sulfite Chemical class [O-]S([O-])=O LSNNMFCWUKXFEE-UHFFFAOYSA-L 0.000 description 1
- 150000003573 thiols Chemical class 0.000 description 1
- NJRXVEJTAYWCQJ-UHFFFAOYSA-N thiomalic acid Chemical compound OC(=O)CC(S)C(O)=O NJRXVEJTAYWCQJ-UHFFFAOYSA-N 0.000 description 1
- GVPDNFYOFKBFEN-UHFFFAOYSA-N trimethyl(octadecoxy)silane Chemical compound CCCCCCCCCCCCCCCCCCO[Si](C)(C)C GVPDNFYOFKBFEN-UHFFFAOYSA-N 0.000 description 1
- 239000001993 wax Substances 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
- A61K8/498—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
-
- 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
- A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
- A61K8/4986—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with sulfur as the only hetero atom
-
- 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
- A61K8/60—Sugars; Derivatives thereof
-
- 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
Definitions
- the subject of the invention is the use of particular dithiols in a composition for permanent deformation of the hair. It also relates to a process for permanent deformation of the hair using these dithiols, as well as cosmetic compositions containing at least one of these dithiols and at least one compound chosen from surfactants and nonionic, anionic, cationic, amphoteric polymers or zwitterionic or cosmetic compositions containing specific dithiols.
- the technique for carrying out permanent deformation of the hair consists, firstly, in opening the disulfide bonds of keratin (cystine) using a composition containing a reducing agent (reduction step), then after preferably having rinsed the hair, to reconstitute in a second time said disulfide bonds by applying an oxidizing composition (oxidation step, also called fixing) so as to give the hair the desired shape.
- This technique makes it possible indifferently to carry out either the waving of the hair, or their straightening or their straightening, the hair possibly being, as the case may be, tensioned during all or part of the deformation process.
- compositions for carrying out the first stage of a perming operation are generally in the form of lotions, creams, gels, powders to be diluted in a liquid support, and contain a reducing agent, preferably a thiol.
- a reducing agent preferably a thiol.
- those commonly used are cysteine and thioglycolic acid as well as its esters, in particular glycerol monothioglycolate.
- Thioglycolic acid is particularly effective in reducing the disulfide bonds of keratin and can be considered at alkaline pH, in particular in the form of ammonium thioglycolate, as the reference compound permanently.
- a perfume is generally used to mask odors.
- Cysteine produces a much weaker odor than that of thioglycolic acid, but the degree of crimp obtained is much lower and far from satisfactory.
- cysteine requires the use of a very alkaline pH.
- Glycerol monothioglycolate is also very smelly. It is, on the other hand, used at a pH close to neutrality, but its performance is notably lower than that of thioglycolic acid.
- 0204 352 discloses a method of metal cladding conferring, with keratin fibers, residual cosmetic properties to shampoos.
- a composition containing at least one metal salt is applied to the keratin fibers, then a composition containing at least one reducing agent is applied.
- dithiols BMS (bismercaptoethylsulfone), DTT (dithiothreitol), DH (N, N'dimethyl-N, N'-bis (mercaptoacetyl) hydrazine).
- the keratin fibers can be reduced, prior to the application of the composition containing at least one metal salt. It is intended that this reduction can be carried out with one of the reducing agents described in the text of this application, such as the dithiols previously mentioned.
- the problem posed by the invention is to provide a reducing composition, for the permanent deformation of the hair, more effective than those which already exist, in particular in terms of degree, nervousness or quality of curl, while reducing the degradation of the hair.
- this reducing composition must also be practically without effect on an artificial coloring of keratin fibers.
- the invention proposes the use, in order to reduce the disulfide bonds of keratin, in a composition reducing the deformation of the fiber.
- keratin at a pH between 5 and 8.5, of dithiols of formula I, having a solubility in water greater than 0.1 M:
- A is a C3 to C10 hydrocarbon chain, linear or cyclic, saturated or unsaturated, this chain possibly carrying one or more ramifications in C1 to C4 and which can be interrupted by one or more hetero atoms such as sulfur , oxygen, nitrogen, silicon or phosphorus and may also include one or more substituents, such as hydroxyl, amino, carbamate, carbonate, hydrazine, ethers, acids, esters, amide, cyano, ureido groups.
- permanent deformation is understood to mean permanent (permanent) curling, straightening or straightening of the hair.
- A is a hydrocarbon chain comprising from 3 to 8 carbon atoms, and more preferably from 4 to 6 carbon atoms.
- the pH of the reducing composition comprising the dithiols of formula I is between 5.5 and 8.5, and more preferably between 6 and 8.
- the pKa, at 25 ° C., of the dithiol of formula I is less than 9.
- Another subject of the invention relates to a process for permanent deformation of the hair using a reducing composition comprising at least one compound of formula (I).
- R1, R2, R3, R4, R5 and R6 representing independently of each other: H, OH, COOH, NH 2 , a linear or branched C1 to C10 alkyl radical, a linear C2 to C10 alkenyl radical or branched, a linear or branched C2 to C10 alkynyl radical, these radicals being capable of being interrupted by one or more hetero atoms such as sulfur, oxygen, nitrogen, silicon or phosphorus and also being able to comprise one or more several substituents such as hydroxyl, amino, carbamate, carbonate, hydrazine, ether, acid, ester, amide, cyano, ureido groups;
- X O, S or NRl
- the process according to the invention for permanent deformation of the hair comprises the application of a reducing composition comprising, as agent reducing agent, a compound of formula (I).
- a reducing composition comprising, as agent reducing agent, a compound of formula (I).
- the hair is shaped using, for example, mechanical means well known to those skilled in the art, such as curlers, the reducing composition being applied before or after any means of shaping the hair, and a fixing composition being applied after the reducing composition, with or without an intermediate or subsequent rinsing step or application of an intermediate composition.
- the permanent deformation of the hair preferably consists, in a first step, in reducing the disulfide bonds of the keratin by application, for approximately 5 to 60 min, of a reducing composition as defined above, then , in a second step, to reform said bonds by applying an oxidizing composition or, optionally, by allowing the oxygen in the air to act.
- a reducing composition is applied as defined above to wet hair previously wound on rollers having from 4 to 20 mm in diameter, the composition possibly being able to be applied as and as the hair is rolled up; the reducing composition is then left to act for a time from 5 to 60 minutes, preferably from 5 to 30 minutes, then rinsing thoroughly; after which an oxidizing composition is applied to the coiled hair, making it possible to reform the disulphide bonds of the keratin for an exposure time of 2 to 10 minutes. After removing the rollers, rinse
- the laying of the reducing composition can be done under heat.
- the oxidation or oxidizing composition is of the type commonly used and contains, for example, as an oxidizing agent for hydrogen peroxide, an alkali bromate, a persalt, a polythionate or a mixture of alkali bromate and persal.
- concentration of hydrogen peroxide can vary from 1 to 20 volumes and preferably from 1 to 10, the concentration of alkali bromate from 2 to 12% and that of parsley from 0.1 to 15% by weight relative to the total weight of the oxidizing composition.
- the pH of the oxidizing composition is generally between 2 and 10. This oxidation can be carried out immediately or be delayed.
- the deformation of the hair according to the invention may also consist of a process for straightening or straightening the hair, in which a reducing composition according to the invention is applied to the hair, then the hair is subjected to mechanical deformation allowing fix them in their new form, by smoothing the hair with a wide-tooth comb, with the back of a comb or by hand. After an exposure time of 5 to 60 minutes, in particular, from 5 to 30 minutes, we then proceed to a new smoothing, then rinse thoroughly and apply an oxidizing or fixing composition as defined above, which leave on for about 2 to 10 minutes, then rinse the hair thoroughly.
- the reducing agent of general formula (I) is especially present at a concentration of between 0.05 and 30% and, preferably, between 0.1 and 20% by weight relative to the total weight of the reducing composition.
- the pH is obtained using an alkaline agent such as, for example, ammonia, monoethanolamine, diethanolamine, triethanolamine, 1,3-propane diamine, an alkali or ammonium carbonate or bicarbonate, a organic carbonate such as guanidine carbonate, an alkali hydroxide or using an acidifying agent such as for example hydrochloric acid, acetic acid, lactic acid, oxalic acid or boric acid .
- an alkaline agent such as, for example, ammonia, monoethanolamine, diethanolamine, triethanolamine, 1,3-propane diamine, an alkali or ammonium carbonate or bicarbonate, a organic carbonate such as guanidine carbonate, an alkali hydroxide or using an acidifying agent such as for example hydrochloric acid, acetic acid, lactic acid, oxalic acid or boric acid .
- the reducing composition may also contain, in combination, another known reducing agent, such as for example thioglycolic acid, glycerol or glycol monothioglycolate, cysteamine and its acylated C1-C4 derivatives such as N-acetyl cysteamine.
- another known reducing agent such as for example thioglycolic acid, glycerol or glycol monothioglycolate, cysteamine and its acylated C1-C4 derivatives such as N-acetyl cysteamine.
- the reducing composition also contains a surfactant of non-ionic, anionic, cationic or amphoteric type and among these, mention may be made of alkylsulphates, alkylbenzenesulphates, alkylethersulphates, alkylsulphonates, salts of quaternary ammonium, alkyl betaines, oxyethylenated alkylphenols, alkanolamides of fatty acids, esters of oxyethylenated fatty acids and other nonionic surfactants of the hydroxypropylether type.
- a surfactant of non-ionic, anionic, cationic or amphoteric type and among these, mention may be made of alkylsulphates, alkylbenzenesulphates, alkylethersulphates, alkylsulphonates, salts of quaternary ammonium, alkyl betaines, oxyethylenated alkylphenols, alkanolamides of fatty
- the reducing composition contains at least one surfactant, this is generally present at a maximum concentration of 30% by weight, and preferably between 0.5 and 10% by weight relative to the total weight of the reducing composition .
- the reducing composition may also contain a treating agent of cationic, anionic, nonionic or amphoteric nature.
- treating agents include those described in French patents No. 2,598,613 and No. 2,470,596. It is also possible to use, as treating agents, volatile or non-linear or cyclic silicones and their mixtures, polydimethylsiloxanes, quaternized polyorganosiloxanes such as those described in French patent application No. 2,535,730, polyorganosiloxanes with aminoalkyl groups modified by alkoxycarbonyalkyl groups such as those described in US Pat.
- polyalkylbetaine polydimethyl-siloxane described in British patent n ° 2,197,352, organo polysiloxanes modified by mercapto or mercaptoalkyl groups such as those described in French patent n ° 1,530,369 and in European patent application n ° 295,780, as well than silanes such as stearoxytrimethylsilane.
- the reducing composition may also contain other treating ingredients such as cationic polymers such as those used in the compositions of French patents No. 79.32078 (2,472,382) and 80,26421 (2,495,931), or also cationic polymers of the ionene type. such as those used in the compositions of Luxembourg patent no.
- cationic polymers such as those used in the compositions of French patents No. 79.32078 (2,472,382) and 80,26421 (2,495,931)
- cationic polymers of the ionene type such as those used in the compositions of Luxembourg patent no.
- the reducing composition according to the invention is essentially in aqueous form, in particular in the form of a thickened lotion or not, a cream or a gel.
- the reducing composition according to the invention can also be of the exothermic type, that is to say causing a certain heating during application to the hair, which brings pleasure to the person who undergoes the first time of the perm. or straightening.
- the reducing composition according to the invention can also contain a solvent such as for example ethanol, propanol or isopropanol or also glycerol, at a maximum concentration of 20% relative to the total weight of the composition.
- the vehicle for the compositions according to the invention is preferably water or an aqueous-alcoholic solution of a lower alcohol, such as ethanol, isopropanol or butanol.
- the reducing composition is preferably in the form of a thickened cream so as to keep the hair as straight as possible.
- These creams are produced in the form of "heavy" emulsions, for example based on glyceryl stearate, glycol stearate, self-emulsifying waxes or fatty alcohols.
- liquids or gels containing thickening agents such as carboxyvinyl polymers or copolymers which "stick" the hair and keep it in the smooth position during the setting time.
- the invention also relates to cosmetic compositions comprising, in a cosmetically acceptable medium, at least one dithiol of formula I chosen from the compounds of formulas (B), (C), (E), (F), (G), ( H), (I), (J), (L), (M) and (N).
- R1 and R2 represent, independently of each other, H, OH, COOH, NH2, a linear or branched C2 to C10 alkyl radical, a linear C2 to C10 alkenyl radical, a C2 to C10 alkyl radical , linear or branched, these radicals which can be interrupted by one or more heteroatoms such as sulfur, oxygen, nitrogen, silicon or phosphorus, and which can comprise one or more substituents, such as hydroxyl or amino groups, carbamate, carbonate, hydrazine, ether, ester, amide, cyano, ureido; with the restriction that,
- R1 and R2 independently of one another represent a methyl radical or an R1 radical as indicated above,
- Z represents a bond belonging to a C6 carbocycle substituted by one or more Ri groups, identical or different, Ri denoting a methyl radical or an R1 radical, as indicated above other than hydrogen or a bond belonging to a unsubstituted C6 carbocycle if at least one of R1 or R2 is different from a hydrogen atom,
- R3, R4, R5, R6 have, independently of one another, the same meanings as R1 and R2 as indicated above, and can also denote a methyl radical, if R1 and R2 do not denote all two a hydrogen atom or if one of them is at least different from a methyl radical.
- the invention finally relates to cosmetic compositions containing at least one compound of formula I as defined above and at least one compound, chosen from surfactants and nonionic, anionic, cationic, amphoteric or zwitterionic polymers. All these compositions can also contain the additives mentioned above.
- the invention also relates to a kit, in particular, for the permanent deformation of the hair comprising, in a first compartment, as a reducing composition, a composition according to the invention comprising a compound of formula (I), and in a second compartment , an oxidizing composition.
- the above lotion is applied to locks of gray hair containing 90% white hair.
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)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP04742633A EP1680077A2 (fr) | 2003-05-06 | 2004-05-04 | Utilisation de dithiols dans une composition de deformation permanente des cheveux |
US10/555,788 US20070134185A1 (en) | 2003-05-06 | 2004-05-04 | Use of dithiols in a hair-perming composition |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR03/05496 | 2003-05-06 | ||
FR0305496A FR2854568B1 (fr) | 2003-05-06 | 2003-05-06 | Utilisation de dithiols dans une composition de deformation permanente des cheveux |
US47736603P | 2003-06-11 | 2003-06-11 | |
US60/477,366 | 2003-06-11 |
Publications (2)
Publication Number | Publication Date |
---|---|
WO2004098488A2 true WO2004098488A2 (fr) | 2004-11-18 |
WO2004098488A3 WO2004098488A3 (fr) | 2004-12-29 |
Family
ID=33306179
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/FR2004/001071 WO2004098488A2 (fr) | 2003-05-06 | 2004-05-04 | Utilisation de dithiols dans une composition de deformation permanente des cheveux |
Country Status (4)
Country | Link |
---|---|
US (1) | US20070134185A1 (fr) |
EP (1) | EP1680077A2 (fr) |
FR (1) | FR2854568B1 (fr) |
WO (1) | WO2004098488A2 (fr) |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1570834A1 (fr) * | 2004-03-02 | 2005-09-07 | L'oreal | Composition de deformation permanente des cheveux contenant au moins un dicarboxydithiol |
FR2880888A1 (fr) * | 2005-01-20 | 2006-07-21 | Oreal | Utilisation d'aminodithiol en tant qu'agent reducteur pour la deformation permanente des cheveux |
WO2006103860A1 (fr) * | 2005-03-28 | 2006-10-05 | Nakayama, Hiroki | Premier agent sans danger pour agent de permanentage moins agressif envers les cheveux |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20070009462A9 (en) * | 2004-03-02 | 2007-01-11 | Gerard Malle | Composition to permanently reshape the hair containing at least one dicarboxydithiol |
US11147759B2 (en) * | 2017-11-17 | 2021-10-19 | Living Proof, Inc. | Covalent treatment for keratin-containing materials |
CA3091434A1 (fr) * | 2018-02-20 | 2019-08-29 | Living Proof, Inc. | Traitement covalent avec des thiols de materiaux contenant de la keratine |
Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2719813A (en) * | 1953-09-10 | 1955-10-04 | Procter & Gamble | Reducing hair waving lotion |
US3173842A (en) * | 1963-09-03 | 1965-03-16 | Olin Mathieson | Process for waving human hair with 2, 5-dimercaptothiodiazoline |
US3459198A (en) * | 1966-03-10 | 1969-08-05 | Collaborative Res Inc | Waving and straightening human hair with 1,4-dimercapto-2,3-butane diol and substituted products thereof |
GB1260227A (en) * | 1968-04-05 | 1972-01-12 | Oreal | Cosmetic compositions |
US3768490A (en) * | 1972-01-31 | 1973-10-30 | Oreal | Permanently having and permanently setting of hair |
US3809697A (en) * | 1971-10-07 | 1974-05-07 | Mead Johnson & Co | 1,4-bis-acylpiperazines |
US3865546A (en) * | 1970-10-22 | 1975-02-11 | Collaborative Res Inc | Depilatory composition and method of use |
FR2668929A1 (fr) * | 1990-11-09 | 1992-05-15 | Oreal | Composition cosmetique reductrice pour la deformation permanente des cheveux a base d'un amino-mercaptoalkylamide et procede de deformation permanente des cheveux. |
EP0721772A1 (fr) * | 1995-01-12 | 1996-07-17 | Wella Aktiengesellschaft | Agent et procédé pour la déformation permanente des cheveux |
EP1352630A2 (fr) * | 2002-04-08 | 2003-10-15 | L'oreal | Procédé de gainage métallique conférant aux fibres kératiniques des propriétés cosmétiques rémanentes aux shampoings |
-
2003
- 2003-05-06 FR FR0305496A patent/FR2854568B1/fr not_active Expired - Fee Related
-
2004
- 2004-05-04 EP EP04742633A patent/EP1680077A2/fr not_active Withdrawn
- 2004-05-04 WO PCT/FR2004/001071 patent/WO2004098488A2/fr active Application Filing
- 2004-05-04 US US10/555,788 patent/US20070134185A1/en not_active Abandoned
Patent Citations (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2719813A (en) * | 1953-09-10 | 1955-10-04 | Procter & Gamble | Reducing hair waving lotion |
US3173842A (en) * | 1963-09-03 | 1965-03-16 | Olin Mathieson | Process for waving human hair with 2, 5-dimercaptothiodiazoline |
US3459198A (en) * | 1966-03-10 | 1969-08-05 | Collaborative Res Inc | Waving and straightening human hair with 1,4-dimercapto-2,3-butane diol and substituted products thereof |
GB1260227A (en) * | 1968-04-05 | 1972-01-12 | Oreal | Cosmetic compositions |
US3865546A (en) * | 1970-10-22 | 1975-02-11 | Collaborative Res Inc | Depilatory composition and method of use |
US3809697A (en) * | 1971-10-07 | 1974-05-07 | Mead Johnson & Co | 1,4-bis-acylpiperazines |
US3768490A (en) * | 1972-01-31 | 1973-10-30 | Oreal | Permanently having and permanently setting of hair |
FR2668929A1 (fr) * | 1990-11-09 | 1992-05-15 | Oreal | Composition cosmetique reductrice pour la deformation permanente des cheveux a base d'un amino-mercaptoalkylamide et procede de deformation permanente des cheveux. |
EP0721772A1 (fr) * | 1995-01-12 | 1996-07-17 | Wella Aktiengesellschaft | Agent et procédé pour la déformation permanente des cheveux |
EP1352630A2 (fr) * | 2002-04-08 | 2003-10-15 | L'oreal | Procédé de gainage métallique conférant aux fibres kératiniques des propriétés cosmétiques rémanentes aux shampoings |
Non-Patent Citations (6)
Title |
---|
EDWARD R. ATKINSON, G. RICHARD HANDRICK, ROBERT J. BRUNI, FELIX E. GRANCHELLI: "Potential Antiradiation Drugs. I. Amide, hydroxamic acid, and hydrazine derivatives of mercapto acids. Amino thioacids." JOURNAL OF MEDICINAL CHEMISTRY, 1965, pages 29-33, XP002263028 * |
LAMOUREUX G V ET AL: "SYNTHESIS OF DITHIOLS AS REDUCING AGENTS FOR DISULFIDES IN NEUTRAL AQUEOUS SOLUTION AND COMPARISON OF REDUCTION POTENTIALS" JOURNAL OF ORGANIC CHEMISTRY, AMERICAN CHEMICAL SOCIETY. EASTON, US, vol. 58, no. 3, 1993, pages 633-641, XP000999675 ISSN: 0022-3263 * |
SINGH R ET AL: "A REAGENT FOR REDUCTION OF DISULFIDE BONDS IN PROTEINS THAT REDUCESDISULFIDE BONDS FASTER THAN DOES DITHIOTHREITOL" JOURNAL OF ORGANIC CHEMISTRY, AMERICAN CHEMICAL SOCIETY. EASTON, US, vol. 56, no. 7, 29 mars 1991 (1991-03-29), pages 2332-2337, XP000601977 ISSN: 0022-3263 cité dans la demande * |
SZAJEWSKI R P ET AL: "RATE CONSTANTS AND EQUILIBRIUM CONSTANTS FOR THIOL-DISULFIDE INTERCHANGE REACTIONS INVOLVING OXIDIZED GLUTATHIONE" JOURNAL OF THE AMERICAN CHEMICAL SOCIETY, AMERICAN CHEMICAL SOCIETY, WASHINGTON, DC, US, vol. 102, no. 6, 1 mars 1980 (1980-03-01), pages 2011-2025, XP002072983 ISSN: 0002-7863 * |
TERENCE C. OWEN, JAWAD M. FAYADH, JUDY S. CHEN: "Large ring cyclic disulfide diamides" JOURNAL OF ORGANIC CHEMISTRY, vol. 38, no. 5, 1973, pages 937-939, XP002263029 * |
WATSON J. LEES, RAJEEVA SINGH; GEORGES M. WHITESIDES: "meso-2,5-dimercapto-N,N,N',N'-tetramethyl adipamide : A readily available, kineically rapid reagent for the reduction of disulfides in aqueous solution" J. ORG. CHEM., vol. 56, 1991, pages 7328-7331, XP002263027 cité dans la demande * |
Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP1570834A1 (fr) * | 2004-03-02 | 2005-09-07 | L'oreal | Composition de deformation permanente des cheveux contenant au moins un dicarboxydithiol |
FR2880888A1 (fr) * | 2005-01-20 | 2006-07-21 | Oreal | Utilisation d'aminodithiol en tant qu'agent reducteur pour la deformation permanente des cheveux |
WO2006077170A1 (fr) * | 2005-01-20 | 2006-07-27 | L'oreal | Utilisation de l'aminodithiol comme agent reducteur dans la realisation d'une permanente |
WO2006103860A1 (fr) * | 2005-03-28 | 2006-10-05 | Nakayama, Hiroki | Premier agent sans danger pour agent de permanentage moins agressif envers les cheveux |
Also Published As
Publication number | Publication date |
---|---|
FR2854568A1 (fr) | 2004-11-12 |
FR2854568B1 (fr) | 2007-11-02 |
EP1680077A2 (fr) | 2006-07-19 |
WO2004098488A3 (fr) | 2004-12-29 |
US20070134185A1 (en) | 2007-06-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0432051B1 (fr) | Composition cosmétique réductrice pour la permanente des cheveux, à base de cystéamine et/ou de son dérivé N-acétylé et d'un polymère cationique, et son utilisation dans un procédé de déformation permanente des cheveux | |
EP0440547B1 (fr) | Composition cosmétique réductrice pour la déformation permanente des cheveux à base d'un ester de l'acide thioglycolique et de N-acyl(C2-C4)cystéamine et son procédé de mise en oeuvre | |
EP0723772B1 (fr) | Composition réductrice comprenant un acide aminé basique et un polymère cationique | |
FR2654617A1 (fr) | Composition cosmetique reductrice pour permanente contenant, en tant qu'agent reducteur, de l'aletheine ou l'un de ses sels, et son utilisation dans un procede de deformation permanente des cheveux. | |
EP1468667B1 (fr) | Procédé de traitement capillaire et utilisation du procédé pour le lissage des cheveux | |
WO1993001791A1 (fr) | Melange azeotrope de thioglycolate d'hydroxy-2 propyle et de thioglycolate d'hydroxy-2 methyl-1 ethyle, son procede d'obtention et son utilisation dans un procede de deformation permanente des cheveux | |
EP1584329B1 (fr) | Procédé de traitement capillaire et utilisation dudit procédé | |
EP0626166B1 (fr) | Nouveau procédé de déformation permanente des cheveux et composition pour sa mise en oeuvre contenant en association un amino ou amidothiol et au moins un bromure minéral | |
EP0689827B1 (fr) | Procédé pour la déformation permanente des matières kératiniques | |
FR2773071A1 (fr) | Agent reducteur a plusieurs composants et procede de deformation permanente des cheveux le mettant en oeuvre | |
FR2769499A1 (fr) | Procede de deformation permanente des matieres keratiniques sans rincage intermediaire | |
FR2718351A1 (fr) | Procédé pour la déformation permanente des matières kératiniques. | |
FR2923713A1 (fr) | Composition reductrice epaissie. | |
FR2773072A1 (fr) | Agent oxydant a plusieurs composants et procede de deformation permanente des cheveux le mettant en oeuvre | |
EP1680077A2 (fr) | Utilisation de dithiols dans une composition de deformation permanente des cheveux | |
EP1486196B1 (fr) | Composition réductrice pour la déformation permanente des fibres kératiniques et procédé de déformation permanente | |
EP1475076A1 (fr) | Dithiols à fonction amide et leur utilisation pour la transformation de la forme du cheveu | |
EP0568695A1 (fr) | Composition cosmetique pour une permanente des cheveux contenant en tant que reducteur du bromhydrate de cysteine et/ou du bromhydrate de mercapto-2 ethylamine. | |
EP0671158B1 (fr) | Procédé pour la déformation permanente des matières kératiniques | |
EP0941046B1 (fr) | Composition pour la deformation permanente des fibres keratiniques, obtention et mise en oeuvre | |
EP0884998B2 (fr) | Nouveau procede pour la deformation permanente des matieres keratiniques | |
FR2675046A1 (fr) | Composition cosmetique pour la deformation permanente des cheveux contenant l'association de cysteamine et de n-acetylcysteamine. | |
FR2657254A1 (fr) | Composition cosmetique reductrice pour la permanente des cheveux, a base de n-acetylcysteamine et d'un polymere cationique, et son utilisation dans un procede de deformation permanente des cheveux. | |
FR2939672A1 (fr) | Composition cosmetique comprenant un compose hererocyclique disulfure et un agent reducteur et procede pour la deformation permanente des fibres keratiniques. | |
FR2868304A1 (fr) | Procede de traitement capillaire et utilisation dudit procede |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A2 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BW BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE EG ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NA NI NO NZ OM PG PH PL PT RO RU SC SD SE SG SK SL SY TJ TM TN TR TT TZ UA UG US UZ VC VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A2 Designated state(s): GM KE LS MW MZ NA SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HU IE IT LU MC NL PL PT RO SE SI SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2004742633 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2006500167 Country of ref document: JP |
|
WWP | Wipo information: published in national office |
Ref document number: 2004742633 Country of ref document: EP |
|
WWE | Wipo information: entry into national phase |
Ref document number: 2007134185 Country of ref document: US Ref document number: 10555788 Country of ref document: US |
|
WWP | Wipo information: published in national office |
Ref document number: 10555788 Country of ref document: US |