NO310187B1 - Anvendelse av oksydative hårfarvemidler samt de anvendte midler - Google Patents
Anvendelse av oksydative hårfarvemidler samt de anvendte midler Download PDFInfo
- Publication number
- NO310187B1 NO310187B1 NO19982772A NO982772A NO310187B1 NO 310187 B1 NO310187 B1 NO 310187B1 NO 19982772 A NO19982772 A NO 19982772A NO 982772 A NO982772 A NO 982772A NO 310187 B1 NO310187 B1 NO 310187B1
- Authority
- NO
- Norway
- Prior art keywords
- group
- aminophenol
- hydrogen
- groups
- oxidation dye
- Prior art date
Links
- 239000000118 hair dye Substances 0.000 title claims description 11
- 230000001590 oxidative effect Effects 0.000 title abstract description 5
- 239000003795 chemical substances by application Substances 0.000 title description 5
- 150000003839 salts Chemical class 0.000 claims abstract description 15
- 239000001257 hydrogen Substances 0.000 claims abstract description 11
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 11
- 238000004043 dyeing Methods 0.000 claims abstract description 10
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 claims abstract description 3
- 150000001767 cationic compounds Chemical class 0.000 claims abstract description 3
- 150000002892 organic cations Chemical class 0.000 claims abstract description 3
- 150000002431 hydrogen Chemical group 0.000 claims abstract 4
- 239000000975 dye Substances 0.000 claims description 42
- 230000003647 oxidation Effects 0.000 claims description 29
- 238000007254 oxidation reaction Methods 0.000 claims description 29
- -1 p-toluylenediamine Chemical compound 0.000 claims description 24
- 230000008878 coupling Effects 0.000 claims description 9
- 238000010168 coupling process Methods 0.000 claims description 9
- 238000005859 coupling reaction Methods 0.000 claims description 9
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical class NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 8
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 6
- 102000011782 Keratins Human genes 0.000 claims description 6
- 108010076876 Keratins Proteins 0.000 claims description 6
- 239000008365 aqueous carrier Substances 0.000 claims description 4
- PZRKPUQWIFJRKZ-UHFFFAOYSA-N pyrimidine-2,4,5,6-tetramine Chemical group NC1=NC(N)=C(N)C(N)=N1 PZRKPUQWIFJRKZ-UHFFFAOYSA-N 0.000 claims description 4
- CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 3
- SYEYEGBZVSWYPK-UHFFFAOYSA-N 2,5,6-triamino-4-hydroxypyrimidine Chemical compound NC1=NC(N)=C(N)C(O)=N1 SYEYEGBZVSWYPK-UHFFFAOYSA-N 0.000 claims description 3
- PZKNKZNLQYKXFV-UHFFFAOYSA-N 4-amino-2-(aminomethyl)phenol Chemical compound NCC1=CC(N)=CC=C1O PZKNKZNLQYKXFV-UHFFFAOYSA-N 0.000 claims description 3
- QGNGOGOOPUYKMC-UHFFFAOYSA-N 4-hydroxy-6-methylaniline Chemical compound CC1=CC(O)=CC=C1N QGNGOGOOPUYKMC-UHFFFAOYSA-N 0.000 claims description 3
- 210000004209 hair Anatomy 0.000 abstract description 16
- 238000004040 coloring Methods 0.000 abstract description 6
- 239000000835 fiber Substances 0.000 abstract description 5
- 238000000034 method Methods 0.000 abstract description 5
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract description 3
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000002853 C1-C4 hydroxyalkyl group Chemical group 0.000 abstract 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 1
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 1
- 229910052801 chlorine Inorganic materials 0.000 abstract 1
- 239000000460 chlorine Substances 0.000 abstract 1
- 239000007822 coupling agent Substances 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 239000011737 fluorine Substances 0.000 abstract 1
- 229910052736 halogen Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 239000000047 product Substances 0.000 description 26
- 125000004432 carbon atom Chemical group C* 0.000 description 21
- 125000000217 alkyl group Chemical group 0.000 description 13
- 150000001875 compounds Chemical class 0.000 description 13
- 239000000126 substance Substances 0.000 description 13
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- 239000000194 fatty acid Substances 0.000 description 11
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- 238000002844 melting Methods 0.000 description 8
- 230000008018 melting Effects 0.000 description 8
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 7
- 239000002253 acid Substances 0.000 description 7
- 239000002243 precursor Substances 0.000 description 7
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- 125000002252 acyl group Chemical group 0.000 description 6
- 239000000203 mixture Substances 0.000 description 6
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- 239000006071 cream Substances 0.000 description 5
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- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 5
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- 239000002888 zwitterionic surfactant Substances 0.000 description 5
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- JJNFZRUXEGMNPB-UHFFFAOYSA-N 4-amino-2-[3-(5-amino-2-hydroxyphenoxy)-2-hydroxypropoxy]phenol Chemical compound NC1=CC=C(O)C(OCC(O)COC=2C(=CC=C(N)C=2)O)=C1 JJNFZRUXEGMNPB-UHFFFAOYSA-N 0.000 description 4
- DHMQDGOQFOQNFH-UHFFFAOYSA-M Aminoacetate Chemical compound NCC([O-])=O DHMQDGOQFOQNFH-UHFFFAOYSA-M 0.000 description 4
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- 108010009736 Protein Hydrolysates Proteins 0.000 description 4
- 125000000129 anionic group Chemical group 0.000 description 4
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- 239000003093 cationic surfactant Substances 0.000 description 4
- 238000003776 cleavage reaction Methods 0.000 description 4
- 150000002148 esters Chemical class 0.000 description 4
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- 239000003531 protein hydrolysate Substances 0.000 description 4
- 230000007017 scission Effects 0.000 description 4
- 239000002453 shampoo Substances 0.000 description 4
- LPXPTNMVRIOKMN-UHFFFAOYSA-M sodium nitrite Chemical compound [Na+].[O-]N=O LPXPTNMVRIOKMN-UHFFFAOYSA-M 0.000 description 4
- MKFYOQCXVFXJLY-UHFFFAOYSA-N 3-(5-amino-2-hydroxyphenyl)prop-2-enoic acid Chemical compound NC1=CC=C(O)C(C=CC(O)=O)=C1 MKFYOQCXVFXJLY-UHFFFAOYSA-N 0.000 description 3
- HLIGKHFHQXRAOX-UHFFFAOYSA-N 4-amino-2-[(5-amino-2-hydroxyphenyl)methyl]phenol Chemical compound NC1=CC=C(O)C(CC=2C(=CC=C(N)C=2)O)=C1 HLIGKHFHQXRAOX-UHFFFAOYSA-N 0.000 description 3
- MLOWBZBJSCVWIM-UHFFFAOYSA-N 4-amino-2-[2-[2-(5-amino-2-hydroxyphenoxy)ethoxy]ethoxy]phenol Chemical compound NC1=CC=C(O)C(OCCOCCOC=2C(=CC=C(N)C=2)O)=C1 MLOWBZBJSCVWIM-UHFFFAOYSA-N 0.000 description 3
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- 239000004480 active ingredient Substances 0.000 description 3
- 229910052783 alkali metal Inorganic materials 0.000 description 3
- 150000001340 alkali metals Chemical class 0.000 description 3
- 125000003277 amino group Chemical group 0.000 description 3
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 3
- 150000001805 chlorine compounds Chemical class 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
- 239000003086 colorant Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 150000003840 hydrochlorides Chemical class 0.000 description 3
- 238000004519 manufacturing process Methods 0.000 description 3
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- XDOFQFKRPWOURC-UHFFFAOYSA-N 16-methylheptadecanoic acid Chemical compound CC(C)CCCCCCCCCCCCCCC(O)=O XDOFQFKRPWOURC-UHFFFAOYSA-N 0.000 description 2
- MQCPOLNSJCWPGT-UHFFFAOYSA-N 2,2'-Bisphenol F Chemical compound OC1=CC=CC=C1CC1=CC=CC=C1O MQCPOLNSJCWPGT-UHFFFAOYSA-N 0.000 description 2
- XYRDGCCCBJITBH-UHFFFAOYSA-N 3-amino-2-chloro-6-methylphenol Chemical compound CC1=CC=C(N)C(Cl)=C1O XYRDGCCCBJITBH-UHFFFAOYSA-N 0.000 description 2
- VTXBLQLZQLHDIL-UHFFFAOYSA-N 4-(3-hydroxypropylamino)-3-nitrophenol Chemical compound OCCCNC1=CC=C(O)C=C1[N+]([O-])=O VTXBLQLZQLHDIL-UHFFFAOYSA-N 0.000 description 2
- MWKPYVXITDAZLL-UHFFFAOYSA-N 4-[3-(2,4-diaminophenoxy)propoxy]benzene-1,3-diamine Chemical compound NC1=CC(N)=CC=C1OCCCOC1=CC=C(N)C=C1N MWKPYVXITDAZLL-UHFFFAOYSA-N 0.000 description 2
- DSVRZWSDAPTPDQ-UHFFFAOYSA-N 4-amino-2-(2-hydroxyethoxy)phenol Chemical compound NC1=CC=C(O)C(OCCO)=C1 DSVRZWSDAPTPDQ-UHFFFAOYSA-N 0.000 description 2
- QFVGPSHFQVBCOP-UHFFFAOYSA-N 4-amino-2-[2-[2-[2-(5-amino-2-hydroxyphenoxy)ethoxy]ethoxy]ethoxy]phenol Chemical compound NC1=CC=C(O)C(OCCOCCOCCOC=2C(=CC=C(N)C=2)O)=C1 QFVGPSHFQVBCOP-UHFFFAOYSA-N 0.000 description 2
- AGIJSEBXZWSACU-UHFFFAOYSA-N 4-amino-2-[3-(5-amino-2-hydroxyphenoxy)propoxy]phenol Chemical compound NC1=CC=C(O)C(OCCCOC=2C(=CC=C(N)C=2)O)=C1 AGIJSEBXZWSACU-UHFFFAOYSA-N 0.000 description 2
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- 125000001033 ether group Chemical group 0.000 description 2
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- 239000011713 pantothenic acid Substances 0.000 description 1
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- 239000011619 pantothenol Substances 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- JRKICGRDRMAZLK-UHFFFAOYSA-L persulfate group Chemical group S(=O)(=O)([O-])OOS(=O)(=O)[O-] JRKICGRDRMAZLK-UHFFFAOYSA-L 0.000 description 1
- 125000002467 phosphate group Chemical group [H]OP(=O)(O[H])O[*] 0.000 description 1
- 150000003904 phospholipids Chemical class 0.000 description 1
- QXYMVUZOGFVPGH-UHFFFAOYSA-N picramic acid Chemical compound NC1=CC([N+]([O-])=O)=CC([N+]([O-])=O)=C1O QXYMVUZOGFVPGH-UHFFFAOYSA-N 0.000 description 1
- 239000000419 plant extract Substances 0.000 description 1
- 229920000435 poly(dimethylsiloxane) Polymers 0.000 description 1
- 229920001521 polyalkylene glycol ether Polymers 0.000 description 1
- 229920000573 polyethylene Polymers 0.000 description 1
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 1
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
- 239000011591 potassium Substances 0.000 description 1
- 150000003142 primary aromatic amines Chemical class 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 description 1
- ZZYXNRREDYWPLN-UHFFFAOYSA-N pyridine-2,3-diamine Chemical class NC1=CC=CN=C1N ZZYXNRREDYWPLN-UHFFFAOYSA-N 0.000 description 1
- DQAKJEWZWDQURW-UHFFFAOYSA-N pyrrolidonecarboxylic acid Chemical class OC(=O)N1CCCC1=O DQAKJEWZWDQURW-UHFFFAOYSA-N 0.000 description 1
- 150000003856 quaternary ammonium compounds Chemical class 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 229940001941 soy protein Drugs 0.000 description 1
- 239000008107 starch Substances 0.000 description 1
- 235000019698 starch Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000010902 straw Substances 0.000 description 1
- 229950000244 sulfanilic acid Drugs 0.000 description 1
- BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
- 230000008961 swelling Effects 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- PMOWTIHVNWZYFI-AATRIKPKSA-N trans-2-coumaric acid Chemical compound OC(=O)\C=C\C1=CC=CC=C1O PMOWTIHVNWZYFI-AATRIKPKSA-N 0.000 description 1
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- FAGMGMRSURYROS-UHFFFAOYSA-M trihexadecyl(methyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCC[N+](C)(CCCCCCCCCCCCCCCC)CCCCCCCCCCCCCCCC FAGMGMRSURYROS-UHFFFAOYSA-M 0.000 description 1
- OEIXGLMQZVLOQX-UHFFFAOYSA-N trimethyl-[3-(prop-2-enoylamino)propyl]azanium;chloride Chemical compound [Cl-].C[N+](C)(C)CCCNC(=O)C=C OEIXGLMQZVLOQX-UHFFFAOYSA-N 0.000 description 1
- DWKARHJHPSUOBW-UHFFFAOYSA-N trimethyl-[3-[(2e)-2-(3-methyl-5-oxo-1-phenylpyrazol-4-ylidene)hydrazinyl]phenyl]azanium;chloride Chemical compound [Cl-].CC1=NN(C=2C=CC=CC=2)C(O)=C1N=NC1=CC=CC([N+](C)(C)C)=C1 DWKARHJHPSUOBW-UHFFFAOYSA-N 0.000 description 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 150000003672 ureas Chemical class 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 210000002268 wool Anatomy 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- PICXIOQBANWBIZ-UHFFFAOYSA-N zinc;1-oxidopyridine-2-thione Chemical compound [Zn+2].[O-]N1C=CC=CC1=S.[O-]N1C=CC=CC1=S PICXIOQBANWBIZ-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q5/00—Preparations for care of the hair
- A61Q5/10—Preparations for permanently dyeing the hair
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/415—Aminophenols
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C215/00—Compounds containing amino and hydroxy groups bound to the same carbon skeleton
- C07C215/74—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
- C07C215/76—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton of the same non-condensed six-membered aromatic ring
- C07C215/80—Compounds containing amino and hydroxy groups bound to the same carbon skeleton having hydroxy groups and amino groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton of the same non-condensed six-membered aromatic ring containing at least two amino groups bound to the carbon skeleton
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C217/00—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton
- C07C217/78—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
- C07C217/80—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings
- C07C217/82—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring
- C07C217/84—Compounds containing amino and etherified hydroxy groups bound to the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton having amino groups and etherified hydroxy groups bound to carbon atoms of non-condensed six-membered aromatic rings of the same non-condensed six-membered aromatic ring the oxygen atom of at least one of the etherified hydroxy groups being further bound to an acyclic carbon atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C229/00—Compounds containing amino and carboxyl groups bound to the same carbon skeleton
- C07C229/40—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton
- C07C229/44—Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino groups bound to carbon atoms of at least one six-membered aromatic ring and carboxyl groups bound to acyclic carbon atoms of the same carbon skeleton with carboxyl groups linked to the six-membered aromatic ring, or to the condensed ring system containing that ring, by unsaturated carbon chains
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P1/00—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed
- D06P1/32—General processes of dyeing or printing textiles, or general processes of dyeing leather, furs, or solid macromolecular substances in any form, classified according to the dyes, pigments, or auxiliary substances employed using oxidation dyes
-
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06P—DYEING OR PRINTING TEXTILES; DYEING LEATHER, FURS OR SOLID MACROMOLECULAR SUBSTANCES IN ANY FORM
- D06P3/00—Special processes of dyeing or printing textiles, or dyeing leather, furs, or solid macromolecular substances in any form, classified according to the material treated
- D06P3/02—Material containing basic nitrogen
- D06P3/04—Material containing basic nitrogen containing amide groups
- D06P3/08—Material containing basic nitrogen containing amide groups using oxidation dyes
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Textile Engineering (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Birds (AREA)
- Epidemiology (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19607751A DE19607751A1 (de) | 1996-02-29 | 1996-02-29 | Neue Aminophenol-Derivate und deren Verwendung |
| PCT/EP1997/000767 WO1997031886A1 (fr) | 1996-02-29 | 1997-02-19 | Derives d'aminophenol et leur utilisation dans des colorants d'oxydation pour les cheveux |
Publications (3)
| Publication Number | Publication Date |
|---|---|
| NO982772D0 NO982772D0 (no) | 1998-06-16 |
| NO982772L NO982772L (no) | 1998-06-16 |
| NO310187B1 true NO310187B1 (no) | 2001-06-05 |
Family
ID=7786830
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NO19982772A NO310187B1 (no) | 1996-02-29 | 1998-06-16 | Anvendelse av oksydative hårfarvemidler samt de anvendte midler |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US6635241B1 (fr) |
| EP (1) | EP0883598B1 (fr) |
| JP (1) | JP3924323B2 (fr) |
| AT (1) | ATE247626T1 (fr) |
| AU (1) | AU716438B2 (fr) |
| BR (1) | BR9707886A (fr) |
| CA (1) | CA2248261A1 (fr) |
| CZ (1) | CZ274698A3 (fr) |
| DE (2) | DE19607751A1 (fr) |
| ES (1) | ES2205172T3 (fr) |
| NO (1) | NO310187B1 (fr) |
| PL (1) | PL186724B1 (fr) |
| SK (1) | SK116598A3 (fr) |
| WO (1) | WO1997031886A1 (fr) |
Families Citing this family (14)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2766179B1 (fr) * | 1997-07-16 | 2000-03-17 | Oreal | Nouvelles bases d'oxydation cationiques, leur utilisation pour la teinture d'oxydation des fibres keratiniques, compositions tinctoriales et procedes de teinture |
| FR2767685B1 (fr) * | 1997-09-01 | 2004-12-17 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant du 2-chloro 6-methyl 3-aminophenol et une base d'oxydation, et procede de teinture |
| FR2767686B1 (fr) * | 1997-09-01 | 2004-12-17 | Oreal | Composition pour la teinture d'oxydation des fibres keratiniques comprenant du 2-chloro 6-methyl 3-aminophenol et deux bases d'oxydation, et procede de teinture |
| DE19951009A1 (de) * | 1999-10-22 | 2001-04-26 | Henkel Kgaa | Mittel zum Färben von keratinhaltigen Fasern |
| DE19951008A1 (de) * | 1999-10-22 | 2001-04-26 | Henkel Kgaa | Neue Aminophenol-Derivate und deren Verwendung |
| DE10022829B4 (de) | 2000-05-10 | 2004-02-05 | Wella Ag | p-Aminophenol-Derivate und diese Verbindungen enthaltende Haarfärbemittel |
| DE10022828A1 (de) | 2000-05-10 | 2001-11-22 | Wella Ag | Neue p-Aminophenole und diese Verbindungen enthaltende Färbemittel |
| DE10115994A1 (de) * | 2001-03-30 | 2002-10-10 | Wella Ag | (p-Amino-hydroxyphenyl)acrylamid-Derivate und diese Verbindungen enthaltende Färbemittel |
| WO2003041670A1 (fr) * | 2001-11-17 | 2003-05-22 | Henkel Kommanditgesellschaft Auf Aktien | Colorants d'oxydation a base de revelateurs bicycliques |
| DE10156667A1 (de) | 2001-11-17 | 2003-05-28 | Henkel Kgaa | Oxidationsfärbemittel auf der Basis zweikerniger Entwicklerkomponenten |
| US7772352B2 (en) * | 2005-01-28 | 2010-08-10 | Bezwada Biomedical Llc | Bioabsorbable and biocompatible polyurethanes and polyamides for medical devices |
| DE102010051725A1 (de) * | 2010-11-19 | 2012-05-24 | Merck Patent Gmbh | Verwendung von Ascorbinsäurederivaten zur Färbung von keratinhaltigen Fasern |
| SG192673A1 (en) | 2011-02-10 | 2013-09-30 | Roche Glycart Ag | Mutant interleukin-2 polypeptides |
| EA201892619A1 (ru) | 2011-04-29 | 2019-04-30 | Роше Гликарт Аг | Иммуноконъюгаты, содержащие мутантные полипептиды интерлейкина-2 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE82445C (fr) | ||||
| GB1185045A (en) | 1966-11-03 | 1970-03-18 | Ici Ltd | Amine Derivatives |
| FR1543690A (fr) | 1966-11-03 | 1968-10-25 | Ici Ltd | Procédé de fabrication de nouvelles alcanolamines et de leurs dérivés |
| US3862976A (en) * | 1972-07-31 | 1975-01-28 | Morton Norwich Products Inc | Isocyanophenyl carbamates |
| DE2518393A1 (de) | 1975-04-25 | 1976-11-04 | Henkel & Cie Gmbh | Haarfaerbemittel |
| DE2852272A1 (de) | 1978-12-02 | 1980-06-19 | Henkel Kgaa | Neue entwicklerkomponenten fuer oxidationshaarfarben, deren herstellung sowie diese enthaltende haarfaerbemittel |
| DE3723354A1 (de) | 1987-07-15 | 1989-01-26 | Henkel Kgaa | Sulfatierte hydroxy-mischether, verfahren zu ihrer herstellung und ihre verwendung |
| DE3725030A1 (de) | 1987-07-29 | 1989-02-09 | Henkel Kgaa | Oberflaechenaktive hydroxysulfonate |
| FR2628104B1 (fr) | 1988-03-03 | 1990-07-27 | Oreal | Para-aminophenols 3-substitues, leur procede de preparation, leur utilisation pour la teinture des fibres keratiniques et les composes intermediaires utilises dans le procede de preparation |
| DE3926344A1 (de) | 1989-08-09 | 1991-02-28 | Henkel Kgaa | Verfahren zur herstellung von hellfarbigen oelsaeuresulfonaten |
| DE4102907A1 (de) | 1991-01-31 | 1992-08-06 | Henkel Kgaa | 2,5-diaminophenoxy-oxaalkane und deren verwendung als oxidationsfarbstoffvorprodukte |
| DE4344551A1 (de) | 1993-12-24 | 1995-06-29 | Henkel Kgaa | Verwendung von Allylaminophenolen in Oxidationsfärbemitteln |
-
1996
- 1996-02-29 DE DE19607751A patent/DE19607751A1/de not_active Withdrawn
-
1997
- 1997-02-19 AU AU17918/97A patent/AU716438B2/en not_active Ceased
- 1997-02-19 WO PCT/EP1997/000767 patent/WO1997031886A1/fr active IP Right Grant
- 1997-02-19 SK SK1165-98A patent/SK116598A3/sk unknown
- 1997-02-19 PL PL97327541A patent/PL186724B1/pl not_active IP Right Cessation
- 1997-02-19 DE DE59710614T patent/DE59710614D1/de not_active Expired - Lifetime
- 1997-02-19 JP JP53055597A patent/JP3924323B2/ja not_active Expired - Fee Related
- 1997-02-19 ES ES97903318T patent/ES2205172T3/es not_active Expired - Lifetime
- 1997-02-19 CZ CZ982746A patent/CZ274698A3/cs unknown
- 1997-02-19 US US09/125,844 patent/US6635241B1/en not_active Expired - Lifetime
- 1997-02-19 CA CA002248261A patent/CA2248261A1/fr not_active Abandoned
- 1997-02-19 BR BR9707886A patent/BR9707886A/pt unknown
- 1997-02-19 AT AT97903318T patent/ATE247626T1/de active
- 1997-02-19 EP EP97903318A patent/EP0883598B1/fr not_active Expired - Lifetime
-
1998
- 1998-06-16 NO NO19982772A patent/NO310187B1/no not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| AU1791897A (en) | 1997-09-16 |
| PL327541A1 (en) | 1998-12-21 |
| ES2205172T3 (es) | 2004-05-01 |
| US6635241B1 (en) | 2003-10-21 |
| CA2248261A1 (fr) | 1997-09-04 |
| WO1997031886A1 (fr) | 1997-09-04 |
| NO982772D0 (no) | 1998-06-16 |
| PL186724B1 (pl) | 2004-02-27 |
| DE19607751A1 (de) | 1997-09-04 |
| CZ274698A3 (cs) | 1999-03-17 |
| AU716438B2 (en) | 2000-02-24 |
| NO982772L (no) | 1998-06-16 |
| DE59710614D1 (de) | 2003-09-25 |
| EP0883598B1 (fr) | 2003-08-20 |
| SK116598A3 (en) | 1999-02-11 |
| BR9707886A (pt) | 1999-07-27 |
| ATE247626T1 (de) | 2003-09-15 |
| JP3924323B2 (ja) | 2007-06-06 |
| JP2000506836A (ja) | 2000-06-06 |
| EP0883598A1 (fr) | 1998-12-16 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| MM1K | Lapsed by not paying the annual fees |
Free format text: LAPSED IN AUGUST 2002 |