LU87378A1 - Mercapto-4 butyramides n-mono ou n,n-disubstitues par un radical mono ou polyhydroxyalkyle,et leur utilisation en tant qu'agents reducteurs dans un procede de deformation permanente des cheveux - Google Patents
Mercapto-4 butyramides n-mono ou n,n-disubstitues par un radical mono ou polyhydroxyalkyle,et leur utilisation en tant qu'agents reducteurs dans un procede de deformation permanente des cheveux Download PDFInfo
- Publication number
- LU87378A1 LU87378A1 LU87378A LU87378A LU87378A1 LU 87378 A1 LU87378 A1 LU 87378A1 LU 87378 A LU87378 A LU 87378A LU 87378 A LU87378 A LU 87378A LU 87378 A1 LU87378 A1 LU 87378A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- mercapto
- mono
- composition
- butyramide
- reducing
- Prior art date
Links
- 239000003638 chemical reducing agent Substances 0.000 title claims abstract description 16
- 238000000034 method Methods 0.000 title claims abstract description 16
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims abstract description 16
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 13
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 12
- SLFZWKBTTILTLU-UHFFFAOYSA-N 4-sulfanylbutanamide Chemical class NC(=O)CCCS SLFZWKBTTILTLU-UHFFFAOYSA-N 0.000 claims abstract description 10
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 8
- 239000001301 oxygen Substances 0.000 claims abstract description 8
- 150000001875 compounds Chemical class 0.000 claims abstract description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims abstract description 3
- 125000004193 piperazinyl group Chemical group 0.000 claims abstract description 3
- 239000000203 mixture Substances 0.000 claims description 62
- 230000001603 reducing effect Effects 0.000 claims description 26
- -1 alkyl radical Chemical class 0.000 claims description 20
- DNSISZSEWVHGLH-UHFFFAOYSA-N butanamide Chemical class CCCC(N)=O DNSISZSEWVHGLH-UHFFFAOYSA-N 0.000 claims description 18
- 150000001412 amines Chemical class 0.000 claims description 17
- 230000001590 oxidative effect Effects 0.000 claims description 14
- 150000003254 radicals Chemical class 0.000 claims description 13
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 12
- 239000002304 perfume Substances 0.000 claims description 12
- 238000002360 preparation method Methods 0.000 claims description 11
- 238000006243 chemical reaction Methods 0.000 claims description 10
- HZAXFHJVJLSVMW-UHFFFAOYSA-N 2-Aminoethan-1-ol Chemical group NCCO HZAXFHJVJLSVMW-UHFFFAOYSA-N 0.000 claims description 9
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims description 6
- MYMOFIZGZYHOMD-UHFFFAOYSA-N Dioxygen Chemical compound O=O MYMOFIZGZYHOMD-UHFFFAOYSA-N 0.000 claims description 6
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 claims description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 claims description 6
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical compound CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 claims description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 claims description 6
- 229910052717 sulfur Inorganic materials 0.000 claims description 6
- 125000004434 sulfur atom Chemical group 0.000 claims description 6
- 102000011782 Keratins Human genes 0.000 claims description 5
- 108010076876 Keratins Proteins 0.000 claims description 5
- 239000003795 chemical substances by application Substances 0.000 claims description 5
- MBBZMMPHUWSWHV-BDVNFPICSA-N N-methylglucamine Chemical compound CNC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO MBBZMMPHUWSWHV-BDVNFPICSA-N 0.000 claims description 4
- 239000002537 cosmetic Substances 0.000 claims description 4
- ZBCBWPMODOFKDW-UHFFFAOYSA-N diethanolamine Chemical compound OCCNCCO ZBCBWPMODOFKDW-UHFFFAOYSA-N 0.000 claims description 4
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims description 4
- GIAFURWZWWWBQT-UHFFFAOYSA-N 2-(2-aminoethoxy)ethanol Chemical compound NCCOCCO GIAFURWZWWWBQT-UHFFFAOYSA-N 0.000 claims description 3
- WFCSWCVEJLETKA-UHFFFAOYSA-N 2-piperazin-1-ylethanol Chemical compound OCCN1CCNCC1 WFCSWCVEJLETKA-UHFFFAOYSA-N 0.000 claims description 3
- KQIGMPWTAHJUMN-UHFFFAOYSA-N 3-aminopropane-1,2-diol Chemical compound NCC(O)CO KQIGMPWTAHJUMN-UHFFFAOYSA-N 0.000 claims description 3
- 229920006317 cationic polymer Polymers 0.000 claims description 3
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims description 3
- 239000002904 solvent Substances 0.000 claims description 3
- WPWHSFAFEBZWBB-UHFFFAOYSA-N 1-butyl radical Chemical compound [CH2]CCC WPWHSFAFEBZWBB-UHFFFAOYSA-N 0.000 claims description 2
- 239000004902 Softening Agent Substances 0.000 claims description 2
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 claims description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 claims description 2
- 229960003194 meglumine Drugs 0.000 claims description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 2
- 239000003531 protein hydrolysate Substances 0.000 claims description 2
- 239000003093 cationic surfactant Substances 0.000 claims 1
- 229960004592 isopropanol Drugs 0.000 claims 1
- 239000002736 nonionic surfactant Substances 0.000 claims 1
- 238000002407 reforming Methods 0.000 claims 1
- PXQLVRUNWNTZOS-UHFFFAOYSA-N sulfanyl Chemical class [SH] PXQLVRUNWNTZOS-UHFFFAOYSA-N 0.000 claims 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 229910001868 water Inorganic materials 0.000 description 18
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 16
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 12
- 239000012298 atmosphere Substances 0.000 description 9
- 239000000047 product Substances 0.000 description 9
- 150000003573 thiols Chemical class 0.000 description 8
- 239000007788 liquid Substances 0.000 description 7
- MHAJPDPJQMAIIY-UHFFFAOYSA-N Hydrogen peroxide Chemical compound OO MHAJPDPJQMAIIY-UHFFFAOYSA-N 0.000 description 5
- JVTAAEKCZFNVCJ-UHFFFAOYSA-N Lactic Acid Natural products CC(O)C(O)=O JVTAAEKCZFNVCJ-UHFFFAOYSA-N 0.000 description 5
- 239000004310 lactic acid Substances 0.000 description 5
- 235000014655 lactic acid Nutrition 0.000 description 5
- 238000001228 spectrum Methods 0.000 description 5
- 239000003381 stabilizer Substances 0.000 description 5
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 4
- 238000000921 elemental analysis Methods 0.000 description 4
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 229910021529 ammonia Inorganic materials 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 238000003556 assay Methods 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
- 239000006071 cream Substances 0.000 description 3
- 235000019645 odor Nutrition 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
- BWGNESOTFCXPMA-UHFFFAOYSA-N Dihydrogen disulfide Chemical compound SS BWGNESOTFCXPMA-UHFFFAOYSA-N 0.000 description 2
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- GLUUGHFHXGJENI-UHFFFAOYSA-N Piperazine Chemical compound C1CNCCN1 GLUUGHFHXGJENI-UHFFFAOYSA-N 0.000 description 2
- 239000003513 alkali Substances 0.000 description 2
- 150000002148 esters Chemical class 0.000 description 2
- 239000000499 gel Substances 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- TUKLILPMNXCNNK-UHFFFAOYSA-N n,n-bis(2-hydroxyethyl)-4-sulfanylbutanamide Chemical compound OCCN(CCO)C(=O)CCCS TUKLILPMNXCNNK-UHFFFAOYSA-N 0.000 description 2
- UOYXGONHNSNMOG-SCVMZPAESA-N n-methyl-n-[(2s,3r,4r,5r)-2,3,4,5,6-pentahydroxyhexyl]-4-sulfanylbutanamide Chemical compound SCCCC(=O)N(C)C[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO UOYXGONHNSNMOG-SCVMZPAESA-N 0.000 description 2
- 230000009965 odorless effect Effects 0.000 description 2
- 230000003647 oxidation Effects 0.000 description 2
- 238000007254 oxidation reaction Methods 0.000 description 2
- 239000011347 resin Substances 0.000 description 2
- 229920005989 resin Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- FERWBXLFSBWTDE-UHFFFAOYSA-N 3-aminobutan-2-ol Chemical compound CC(N)C(C)O FERWBXLFSBWTDE-UHFFFAOYSA-N 0.000 description 1
- DKIDEFUBRARXTE-UHFFFAOYSA-N 3-mercaptopropanoic acid Chemical compound OC(=O)CCS DKIDEFUBRARXTE-UHFFFAOYSA-N 0.000 description 1
- DTRIDVOOPAQEEL-UHFFFAOYSA-N 4-sulfanylbutanoic acid Chemical compound OC(=O)CCCS DTRIDVOOPAQEEL-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-M Bicarbonate Chemical compound OC([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-M 0.000 description 1
- GAWIXWVDTYZWAW-UHFFFAOYSA-N C[CH]O Chemical group C[CH]O GAWIXWVDTYZWAW-UHFFFAOYSA-N 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 description 1
- LEVWYRKDKASIDU-QWWZWVQMSA-N D-cystine Chemical compound OC(=O)[C@H](N)CSSC[C@@H](N)C(O)=O LEVWYRKDKASIDU-QWWZWVQMSA-N 0.000 description 1
- PHOQVHQSTUBQQK-SQOUGZDYSA-N D-glucono-1,5-lactone Chemical compound OC[C@H]1OC(=O)[C@H](O)[C@@H](O)[C@@H]1O PHOQVHQSTUBQQK-SQOUGZDYSA-N 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 206010070835 Skin sensitisation Diseases 0.000 description 1
- 229920002125 Sokalan® Polymers 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 238000007112 amidation reaction Methods 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
- 239000003849 aromatic solvent Substances 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 238000009835 boiling Methods 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 239000013065 commercial product Substances 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 229960003067 cystine Drugs 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 239000008387 emulsifying waxe Substances 0.000 description 1
- 239000000839 emulsion Substances 0.000 description 1
- 150000002191 fatty alcohols Chemical class 0.000 description 1
- 239000012467 final product Substances 0.000 description 1
- 239000003205 fragrance Substances 0.000 description 1
- 235000012209 glucono delta-lactone Nutrition 0.000 description 1
- 229960003681 gluconolactone Drugs 0.000 description 1
- 229940075529 glyceryl stearate Drugs 0.000 description 1
- 229940100242 glycol stearate Drugs 0.000 description 1
- 238000009499 grossing Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 231100001231 less toxic Toxicity 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 238000002844 melting Methods 0.000 description 1
- 230000008018 melting Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- KTAWKMGFQHAPTN-UHFFFAOYSA-N n-(2-hydroxyethyl)-2-sulfanylacetamide Chemical compound OCCNC(=O)CS KTAWKMGFQHAPTN-UHFFFAOYSA-N 0.000 description 1
- VLYWNGFXBQQMAJ-UHFFFAOYSA-N n-(2-hydroxyethyl)-4-sulfanylbutanamide Chemical compound OCCNC(=O)CCCS VLYWNGFXBQQMAJ-UHFFFAOYSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 229920000059 polyethylene glycol stearate Polymers 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000002335 preservative effect Effects 0.000 description 1
- QLNJFJADRCOGBJ-UHFFFAOYSA-N propionamide Chemical compound CCC(N)=O QLNJFJADRCOGBJ-UHFFFAOYSA-N 0.000 description 1
- 229940080818 propionamide Drugs 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 239000011541 reaction mixture Substances 0.000 description 1
- 230000035484 reaction time Effects 0.000 description 1
- 231100000370 skin sensitisation Toxicity 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 150000003464 sulfur compounds Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 239000002562 thickening agent Substances 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
- C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
- C07D295/182—Radicals derived from carboxylic acids
- C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
-
- 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
- A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C323/00—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups
- C07C323/50—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton
- C07C323/51—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton
- C07C323/60—Thiols, sulfides, hydropolysulfides or polysulfides substituted by halogen, oxygen or nitrogen atoms, or by sulfur atoms not being part of thio groups containing thio groups and carboxyl groups bound to the same carbon skeleton having the sulfur atoms of the thio groups bound to acyclic carbon atoms of the carbon skeleton with the carbon atom of at least one of the carboxyl groups bound to nitrogen atoms
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- 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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Priority Applications (7)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU87378A LU87378A1 (fr) | 1988-11-09 | 1988-11-09 | Mercapto-4 butyramides n-mono ou n,n-disubstitues par un radical mono ou polyhydroxyalkyle,et leur utilisation en tant qu'agents reducteurs dans un procede de deformation permanente des cheveux |
| CA002002678A CA2002678A1 (fr) | 1988-11-09 | 1989-11-08 | Mercapto-4 butyramides n-mono ou n,n-disubstitues par un radical mono ou polyhydroxyalkyle, et leur utilisation en tant qu'agents reducteurs dans un procede de deformation permanente des cheveux |
| DE8989403099T DE68903212T2 (de) | 1988-11-09 | 1989-11-09 | 4-mercapto-butyramide-n-mono- oder n,n-disubstituiert durch ein mono- oder polyhydroxyalkyl-radikal und ihre verwendung als reduktionsmittel zur dauernden verformung von haaren. |
| EP89403099A EP0368763B1 (de) | 1988-11-09 | 1989-11-09 | 4-Mercapto-Butyramide-N-mono- oder N,N-disubstituiert durch ein Mono- oder Polyhydroxyalkyl-Radikal und ihre Verwendung als Reduktionsmittel zur dauernden Verformung von Haaren |
| ES89403099T ES2044187T3 (es) | 1988-11-09 | 1989-11-09 | Mercapto-4 butiramidas n-mono o n,n-disubstituidas por un radical mono o polihidroxialquilo, y su utilizacion como agentes reductores en un procedimiento para la deformacion permanente del cabello. |
| JP1292128A JPH02196711A (ja) | 1988-11-09 | 1989-11-09 | モノ又はポリヒドロキシアルキル基でｎ―モノ又はｎ，ｎ―ジ置換された４―メルカプトブチルアミド及びそれを含有する毛髪のパーマネント変形用の還元剤 |
| AT89403099T ATE81504T1 (de) | 1988-11-09 | 1989-11-09 | 4-mercapto-butyramide-n-mono- oder n,ndisubstituiert durch ein mono- oder polyhydroxyalkyl-radikal und ihre verwendung als reduktionsmittel zur dauernden verformung von haaren. |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU87378 | 1988-11-09 | ||
| LU87378A LU87378A1 (fr) | 1988-11-09 | 1988-11-09 | Mercapto-4 butyramides n-mono ou n,n-disubstitues par un radical mono ou polyhydroxyalkyle,et leur utilisation en tant qu'agents reducteurs dans un procede de deformation permanente des cheveux |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU87378A1 true LU87378A1 (fr) | 1990-06-12 |
Family
ID=19731105
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU87378A LU87378A1 (fr) | 1988-11-09 | 1988-11-09 | Mercapto-4 butyramides n-mono ou n,n-disubstitues par un radical mono ou polyhydroxyalkyle,et leur utilisation en tant qu'agents reducteurs dans un procede de deformation permanente des cheveux |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP0368763B1 (de) |
| JP (1) | JPH02196711A (de) |
| AT (1) | ATE81504T1 (de) |
| CA (1) | CA2002678A1 (de) |
| DE (1) | DE68903212T2 (de) |
| ES (1) | ES2044187T3 (de) |
| LU (1) | LU87378A1 (de) |
Families Citing this family (63)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2683999B1 (fr) * | 1991-11-27 | 1994-01-07 | Oreal | Composition cosmetique pour une permanente des cheveux contenant en tant que reducteur du bromhydrate de cysteine et/ou du bromhydrate de mercapto-2 ethylamine. |
| FR2708197B1 (fr) * | 1993-07-28 | 1995-09-08 | Oreal | Nouvelles compositions à base d'eau oxygénée et leur utilisation comme fixateurs pour permanentes. |
| FR2721823B1 (fr) | 1994-06-30 | 1996-08-02 | Oreal | Procede pour la deformation permanente des matieres keratiniques |
| FR2729852A1 (fr) | 1995-01-30 | 1996-08-02 | Oreal | Composition reductrice comprenant un acide amine basique et un polymere cationique |
| DE19618445A1 (de) * | 1996-05-08 | 1997-11-13 | Wella Ag | Mittel und Verfahren zur dauerhaften Haarverformung auf Basis von Mercaptoacetamiden sowie Verfahren zu deren Herstellung |
| DE19732079C1 (de) * | 1997-07-25 | 1999-02-04 | Wella Ag | Gesättigte, alkylsubstituierte N-Mercaptoacetyl-Heterocyclen, Mittel und Verfahren zur dauerhaften Haarverformung auf deren Basis |
| FR2831803B1 (fr) | 2001-11-08 | 2004-07-30 | Oreal | Compositions cosmetiques contenant une silicone aminee et un agent epaississant et leurs utilisations |
| AU2002301803B2 (en) | 2001-11-08 | 2004-09-09 | L'oreal | Cosmetic compositions containing an aminosilicone and a conditioner, and uses thereof |
| FR2831805B1 (fr) | 2001-11-08 | 2004-08-06 | Oreal | Procede de deformation permanente des cheveux mettant en oeuvres des silicones aminees particulieres |
| US7608116B2 (en) | 2002-12-24 | 2009-10-27 | L'oreal S.A. | Oxidation dye composition comprising at least one mesomorphic phase, process for preparing it and ready-to-use composition for dyeing keratin materials |
| US8313737B2 (en) | 2003-04-16 | 2012-11-20 | L'oreal S.A. | Hair treatment process for smoothing the hair |
| FR2868305B1 (fr) | 2004-04-02 | 2006-06-30 | Oreal | Procede de traitement capillaire et utilisation dudit procede |
| FR2868420B1 (fr) * | 2004-04-06 | 2006-06-16 | Oreal | Utilisation de dimercaptoamides pour la deformation permanente des fibres keratiniques |
| FR2879294B1 (fr) | 2004-12-14 | 2007-03-30 | Oreal | Dosage des proteines du cheveu |
| FR2881346B1 (fr) | 2005-01-28 | 2007-04-27 | Oreal | Procede de traitement capillaire et utilisation dudit procede |
| FR2883168B1 (fr) | 2005-03-18 | 2008-01-11 | Oreal | Compositions cosmetiques de soin, renforcement et/ou reparation des substrats keratiniques comprenant des polypeptides kap |
| EP1880707A1 (de) * | 2006-07-21 | 2008-01-23 | Wella Aktiengesellschaft | Verfahren und Zusammensetzung zumr dauerhaften Haarverformung |
| FR2910274B1 (fr) | 2006-12-22 | 2009-04-03 | Oreal | Procede de deformation permanente des fibres keratiniques comprenant une etape d'application d'une composition reductrice faiblement concentree et une etape intermediaire de sechage |
| CN101583400B (zh) * | 2007-01-16 | 2014-02-26 | 荷兰联合利华有限公司 | 毛发矫直组合物 |
| EP2196191A1 (de) | 2008-12-11 | 2010-06-16 | L'oreal | Verfahren zur dauerhaften Verformung von Haaren unter Verwendung einer heterocyclischen Dischwefelverbindung und Wärme |
| FR2944438B1 (fr) | 2009-04-15 | 2011-06-17 | Oreal | Procede de mise en forme des cheveux au moyen d'une composition reductrice et d'un chauffage. |
| WO2011089985A1 (en) | 2010-01-19 | 2011-07-28 | L'oreal | Cosmetic composition for keratin fibers |
| WO2012029529A1 (ja) | 2010-08-31 | 2012-03-08 | 天野エンザイム株式会社 | 酵素を用いた卵殻膜の可溶化方法 |
| WO2012049145A1 (en) | 2010-10-12 | 2012-04-19 | L'oreal | Cosmetic composition comprising a particular silicon derivative and one or more acrylic thickening polymers |
| BR112013021580B1 (pt) | 2011-02-25 | 2019-01-29 | L'oreal | composição cosmética, método para a tintura das fibras queratínicas, método para a tintura e clareamento das fibras queratínicas escuras e dispositivo ou kit de tintura com múltiplos compartimentos |
| FR2971935B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un polymere epaississant, un tensioactif non ionique, un agent alcalin, et un agent reducteur |
| FR2971936B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un tensioactif non ionique, un tensioactif amphotere, un alcool gras ethoxyle, un agent alcalin, et un agent reducteur |
| FR2971939B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un corps gras, un agent alcalin, et un agent reducteur |
| FR2971937B1 (fr) | 2011-02-25 | 2013-02-15 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un polymere epaississant non cellulosique, un agent alcalin, et un agent reducteur |
| FR2971938B1 (fr) | 2011-02-25 | 2013-08-02 | Oreal | Composition pour colorer les fibres keratiniques comprenant un colorant direct a fonction disulfure/thiol, un alcool gras faiblement ou non ethoxyle, un tensioactif cationique, un agent alcalin, et un agent reducteur |
| FR2973661A1 (fr) | 2011-04-08 | 2012-10-12 | Oreal | Procede de traitement des cheveux. |
| FR2977489B1 (fr) | 2011-07-07 | 2014-03-21 | Oreal | Procedes de traitement cosmetique et kit |
| CN104053428A (zh) * | 2012-01-26 | 2014-09-17 | 莱雅公司 | 处理角蛋白纤维的方法 |
| WO2013145330A1 (en) | 2012-03-27 | 2013-10-03 | L'oreal | Process for treating keratin fibers |
| KR102244166B1 (ko) | 2013-09-02 | 2021-04-26 | 로레알 | 양이온성 스티릴 디술파이드 염료를 사용하는 케라틴 섬유 염색 방법, 및 상기 염료를 포함하는 조성물 |
| JP2016088917A (ja) | 2014-11-11 | 2016-05-23 | ロレアル | ケラチン繊維用組成物 |
| KR102090472B1 (ko) | 2015-05-12 | 2020-03-18 | 로레알 | 케라틴 섬유용 조성물 |
| JP7127957B2 (ja) | 2015-05-12 | 2022-08-30 | ロレアル | 熱再成形方法 |
| JP2017025051A (ja) | 2015-07-28 | 2017-02-02 | ロレアル | ケラチン繊維用の組成物、プロセス、方法及び使用 |
| JP7353754B2 (ja) | 2018-12-14 | 2023-10-02 | ロレアル | ケラチン繊維の矯正法 |
| JP2020169122A (ja) | 2019-03-20 | 2020-10-15 | ロレアル | ケラチン繊維を着色するための方法及びキット |
| GB201914233D0 (en) | 2019-10-02 | 2019-11-13 | Bicyclerd Ltd | Phage cyclisation assay |
| FR3111814B1 (fr) | 2020-06-30 | 2023-10-20 | Oreal | Procédé de coloration des fibres kératiniques à partir de poudre et/ou extrait colorant de plantes indigofères et de composés comportant au moins un groupement carbonyle |
| FR3112078B1 (fr) | 2020-07-02 | 2022-08-12 | Oreal | Composition de coloration des fibres kératiniques à partir de composés à motif indole |
| FR3144917B1 (fr) | 2023-01-16 | 2025-10-31 | Oreal | Composition pour lissage amélioré des fibres kératineuses |
| FR3144918B1 (fr) | 2023-01-18 | 2026-01-30 | Oreal | Procédé de lissage amélioré des fibres kératineuses |
| WO2024122393A1 (en) | 2022-12-09 | 2024-06-13 | L'oreal | Composition for improved straightening of keratin fibers |
| US20260191752A1 (en) | 2022-12-09 | 2026-07-09 | L'oreal | Composition suitable for keratin fibers |
| FR3142891B1 (fr) | 2022-12-13 | 2026-06-19 | Oreal | Processus de remodelage à chaud amélioré |
| FR3148718A1 (fr) | 2023-05-19 | 2024-11-22 | L'oreal | Composition et processus de remise en forme de fibres kératineuses |
| FR3152387B3 (fr) | 2023-08-28 | 2025-10-17 | Oreal | Composition adaptée aux fibres kératineuses |
| WO2025018432A1 (en) | 2023-07-20 | 2025-01-23 | L'oreal | Process for treating keratin fibers |
| FR3152385B3 (fr) | 2023-08-28 | 2025-10-24 | Oreal | Composition adaptée aux fibres kératiniques |
| WO2025018433A1 (en) | 2023-07-20 | 2025-01-23 | L'oreal | Process for treating keratin fibers |
| WO2025018430A1 (en) | 2023-07-20 | 2025-01-23 | L'oreal | Composition suitable for keratin fibers |
| FR3152401B3 (fr) | 2023-08-28 | 2025-10-24 | Oreal | Procédé de traitement de fibres kératineuses |
| FR3152386B3 (fr) | 2023-08-30 | 2025-10-24 | Oreal | Composition de traitement des fibres kératineuses |
| WO2025018431A1 (en) | 2023-07-20 | 2025-01-23 | L'oreal | Composition suitable for keratin fibers |
| FR3152391B3 (fr) | 2023-08-28 | 2025-10-24 | Oreal | Processus de traitement des fibres kératineuses |
| FR3152384B3 (fr) | 2023-08-28 | 2025-10-17 | Oreal | Processus de traitement de fibres kératineuses |
| FR3152383B3 (fr) | 2023-08-28 | 2025-10-17 | Oreal | Processus de traitement de fibres kératineuses |
| FR3152382B3 (fr) | 2023-08-28 | 2025-10-17 | Oreal | Procédé de traitement des fibres kératiniques |
| FR3158229B3 (fr) | 2024-01-11 | 2026-02-13 | Oreal | Composition convenant aux fibres kératineuses |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU54233A1 (de) * | 1967-08-02 | 1969-03-24 | ||
| DE2615342C3 (de) * | 1976-04-08 | 1980-06-04 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung von Dithiophosphorsäurediesterhalogeniden |
| AT348542B (de) * | 1977-03-09 | 1979-02-26 | Hoffmann La Roche | Verfahren zur herstellung von neuen thiocarba- moylthiofettsaeuren, deren estern und amiden |
-
1988
- 1988-11-09 LU LU87378A patent/LU87378A1/fr unknown
-
1989
- 1989-11-08 CA CA002002678A patent/CA2002678A1/fr not_active Abandoned
- 1989-11-09 AT AT89403099T patent/ATE81504T1/de not_active IP Right Cessation
- 1989-11-09 EP EP89403099A patent/EP0368763B1/de not_active Expired - Lifetime
- 1989-11-09 JP JP1292128A patent/JPH02196711A/ja active Pending
- 1989-11-09 ES ES89403099T patent/ES2044187T3/es not_active Expired - Lifetime
- 1989-11-09 DE DE8989403099T patent/DE68903212T2/de not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| DE68903212D1 (de) | 1992-11-19 |
| ES2044187T3 (es) | 1994-01-01 |
| EP0368763A1 (de) | 1990-05-16 |
| ATE81504T1 (de) | 1992-10-15 |
| JPH02196711A (ja) | 1990-08-03 |
| CA2002678A1 (fr) | 1990-05-09 |
| EP0368763B1 (de) | 1992-10-14 |
| DE68903212T2 (de) | 1993-02-25 |
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