LU85705A1 - Composition tinctoriale capillaire a base de colorants d'oxydation et de gomme de xanthane - Google Patents

Composition tinctoriale capillaire a base de colorants d'oxydation et de gomme de xanthane Download PDF

Info

Publication number: LU85705A1
Authority: LU; Luxembourg
Prior art keywords: diaminobenzene; methyl; hydroxy; aminobenzene; benzene
Prior art date: 1984-12-21

Application number

LU85705A

Other languages

English (en)

French (fr)

Inventor

Jean-Francois Grollier

Original Assignee

Oreal

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

1984-12-21

Filing date

1984-12-21

Publication date

1986-07-17

1984-12-21 Application filed by Oreal filed Critical Oreal

1984-12-21 Priority to LU85705A priority Critical patent/LU85705A1/fr

1985-12-13 Priority to NL8503442A priority patent/NL8503442A/nl

1985-12-17 Priority to CH5382/85A priority patent/CH667389A5/fr

1985-12-19 Priority to FR8518877A priority patent/FR2575067B1/fr

1985-12-19 Priority to AT0369085A priority patent/AT396550B/de

1985-12-20 Priority to JP60287605A priority patent/JPH0657648B2/ja

1985-12-20 Priority to GB08531462A priority patent/GB2168727B/en

1985-12-20 Priority to IT68089/85A priority patent/IT1193449B/it

1985-12-20 Priority to DE3545371A priority patent/DE3545371C2/de

1985-12-20 Priority to BE0/216041A priority patent/BE903916A/fr

1985-12-20 Priority to CA000498372A priority patent/CA1258634A/fr

1986-07-17 Publication of LU85705A1 publication Critical patent/LU85705A1/fr

1987-12-10 Priority to US07/132,652 priority patent/US4904275A/en

Links

239000000203 mixture Substances 0.000 title claims description 71
230000003647 oxidation Effects 0.000 title claims description 26
238000007254 oxidation reaction Methods 0.000 title claims description 26
239000000975 dye Substances 0.000 claims description 38
239000002243 precursor Substances 0.000 claims description 19
229920001285 xanthan gum Polymers 0.000 claims description 18
239000000230 xanthan gum Substances 0.000 claims description 16
229940082509 xanthan gum Drugs 0.000 claims description 16
235000010493 xanthan gum Nutrition 0.000 claims description 16
PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 claims description 13
UHOVQNZJYSORNB-UHFFFAOYSA-N benzene Substances C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 claims description 10
239000007800 oxidant agent Substances 0.000 claims description 10
-1 3-hydroxyethylamino 3-aminobenzene Chemical compound 0.000 claims description 9
239000000835 fiber Substances 0.000 claims description 9
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 9
150000001875 compounds Chemical class 0.000 claims description 8
CBCKQZAAMUWICA-UHFFFAOYSA-N 1,4-phenylenediamine Chemical compound NC1=CC=C(N)C=C1 CBCKQZAAMUWICA-UHFFFAOYSA-N 0.000 claims description 7
102000011782 Keratins Human genes 0.000 claims description 7
108010076876 Keratins Proteins 0.000 claims description 7
230000001590 oxidative effect Effects 0.000 claims description 7
CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims description 6
CWLKGDAVCFYWJK-UHFFFAOYSA-N 3-aminophenol Chemical compound NC1=CC=CC(O)=C1 CWLKGDAVCFYWJK-UHFFFAOYSA-N 0.000 claims description 6
PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 claims description 6
238000004043 dyeing Methods 0.000 claims description 6
GHMLBKRAJCXXBS-UHFFFAOYSA-N resorcinol Chemical compound OC1=CC=CC(O)=C1 GHMLBKRAJCXXBS-UHFFFAOYSA-N 0.000 claims description 6
WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 claims description 5
QIGBRXMKCJKVMJ-UHFFFAOYSA-N Hydroquinone Chemical compound OC1=CC=C(O)C=C1 QIGBRXMKCJKVMJ-UHFFFAOYSA-N 0.000 claims description 5
229910052700 potassium Inorganic materials 0.000 claims description 5
239000002904 solvent Substances 0.000 claims description 5
LUSZGTFNYDARNI-UHFFFAOYSA-N Sesamol Chemical compound OC1=CC=C2OCOC2=C1 LUSZGTFNYDARNI-UHFFFAOYSA-N 0.000 claims description 4
125000000129 anionic group Chemical group 0.000 claims description 4
125000002091 cationic group Chemical group 0.000 claims description 4
239000003795 chemical substances by application Substances 0.000 claims description 4
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BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims description 3
VQUSUEWNKVODST-UHFFFAOYSA-N 2-(2,4-diaminophenyl)ethanol Chemical compound NC1=CC=C(CCO)C(N)=C1 VQUSUEWNKVODST-UHFFFAOYSA-N 0.000 claims description 3
OBCSAIDCZQSFQH-UHFFFAOYSA-N 2-methyl-1,4-phenylenediamine Chemical compound CC1=CC(N)=CC=C1N OBCSAIDCZQSFQH-UHFFFAOYSA-N 0.000 claims description 3
FLROJJGKUKLCAE-UHFFFAOYSA-N 3-amino-2-methylphenol Chemical compound CC1=C(N)C=CC=C1O FLROJJGKUKLCAE-UHFFFAOYSA-N 0.000 claims description 3
150000001298 alcohols Chemical class 0.000 claims description 3
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239000002304 perfume Substances 0.000 claims description 3
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BAHPQISAXRFLCL-UHFFFAOYSA-N 2,4-Diaminoanisole Chemical compound COC1=CC=C(N)C=C1N BAHPQISAXRFLCL-UHFFFAOYSA-N 0.000 claims description 2
BWAPJIHJXDYDPW-UHFFFAOYSA-N 2,5-dimethyl-p-phenylenediamine Chemical compound CC1=CC(N)=C(C)C=C1N BWAPJIHJXDYDPW-UHFFFAOYSA-N 0.000 claims description 2
RLYCRLGLCUXUPO-UHFFFAOYSA-N 2,6-diaminotoluene Chemical compound CC1=C(N)C=CC=C1N RLYCRLGLCUXUPO-UHFFFAOYSA-N 0.000 claims description 2
MJAVQHPPPBDYAN-UHFFFAOYSA-N 2,6-dimethylbenzene-1,4-diamine Chemical compound CC1=CC(N)=CC(C)=C1N MJAVQHPPPBDYAN-UHFFFAOYSA-N 0.000 claims description 2
KWSVXCAQFTWTEF-UHFFFAOYSA-N 2-(2,5-diaminophenyl)ethanol Chemical compound NC1=CC=C(N)C(CCO)=C1 KWSVXCAQFTWTEF-UHFFFAOYSA-N 0.000 claims description 2
SWZVJOLLQTWFCW-UHFFFAOYSA-N 2-chlorobenzene-1,3-diol Chemical compound OC1=CC=CC(O)=C1Cl SWZVJOLLQTWFCW-UHFFFAOYSA-N 0.000 claims description 2
BVWOHFHLLLPJLH-UHFFFAOYSA-N 2-methoxy-3,5-dimethylbenzene-1,4-diamine Chemical compound COC1=C(C)C(N)=C(C)C=C1N BVWOHFHLLLPJLH-UHFFFAOYSA-N 0.000 claims description 2
HGUYBLVGLMAUFF-UHFFFAOYSA-N 2-methoxybenzene-1,4-diamine Chemical compound COC1=CC(N)=CC=C1N HGUYBLVGLMAUFF-UHFFFAOYSA-N 0.000 claims description 2
NQHVJMJEWQQXBS-UHFFFAOYSA-N 4-ethoxybenzene-1,3-diamine Chemical compound CCOC1=CC=C(N)C=C1N NQHVJMJEWQQXBS-UHFFFAOYSA-N 0.000 claims description 2
ZFIQGRISGKSVAG-UHFFFAOYSA-N 4-methylaminophenol Chemical compound CNC1=CC=C(O)C=C1 ZFIQGRISGKSVAG-UHFFFAOYSA-N 0.000 claims description 2
QPHMVRPABQUYGN-UHFFFAOYSA-N 5-amino-2,4-dichlorophenol Chemical compound NC1=CC(O)=C(Cl)C=C1Cl QPHMVRPABQUYGN-UHFFFAOYSA-N 0.000 claims description 2
PSPYAOSEFGPDOA-UHFFFAOYSA-N 5-ethyl-4-methoxybenzene-1,3-diamine Chemical compound CCC1=CC(N)=CC(N)=C1OC PSPYAOSEFGPDOA-UHFFFAOYSA-N 0.000 claims description 2
JJHVYGVVMBYCMQ-UHFFFAOYSA-N 6-hydroxy-4-methyl-1h-pyridin-2-one Chemical compound CC=1C=C(O)NC(=O)C=1 JJHVYGVVMBYCMQ-UHFFFAOYSA-N 0.000 claims description 2
239000002280 amphoteric surfactant Substances 0.000 claims description 2
229940051880 analgesics and antipyretics pyrazolones Drugs 0.000 claims description 2
239000003963 antioxidant agent Substances 0.000 claims description 2
239000000987 azo dye Substances 0.000 claims description 2
239000000872 buffer Substances 0.000 claims description 2
239000003638 chemical reducing agent Substances 0.000 claims description 2
239000000982 direct dye Substances 0.000 claims description 2
QELUYTUMUWHWMC-UHFFFAOYSA-N edaravone Chemical compound O=C1CC(C)=NN1C1=CC=CC=C1 QELUYTUMUWHWMC-UHFFFAOYSA-N 0.000 claims description 2
LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 2
150000002334 glycols Chemical class 0.000 claims description 2
WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims description 2
ZUVBIBLYOCVYJU-UHFFFAOYSA-N naphthalene-1,7-diol Chemical compound C1=CC=C(O)C2=CC(O)=CC=C21 ZUVBIBLYOCVYJU-UHFFFAOYSA-N 0.000 claims description 2
JRNGUTKWMSBIBF-UHFFFAOYSA-N naphthalene-2,3-diol Chemical compound C1=CC=C2C=C(O)C(O)=CC2=C1 JRNGUTKWMSBIBF-UHFFFAOYSA-N 0.000 claims description 2
DFQICHCWIIJABH-UHFFFAOYSA-N naphthalene-2,7-diol Chemical compound C1=CC(O)=CC2=CC(O)=CC=C21 DFQICHCWIIJABH-UHFFFAOYSA-N 0.000 claims description 2
150000002790 naphthalenes Chemical class 0.000 claims description 2
230000035515 penetration Effects 0.000 claims description 2
150000002989 phenols Chemical class 0.000 claims description 2
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 2
229920000642 polymer Polymers 0.000 claims description 2
JEXVQSWXXUJEMA-UHFFFAOYSA-N pyrazol-3-one Chemical class O=C1C=CN=N1 JEXVQSWXXUJEMA-UHFFFAOYSA-N 0.000 claims description 2
UBUFOHLVTQZEQF-UHFFFAOYSA-N pyridine-2,3,4,6-tetramine Chemical compound NC1=CC(N)=C(N)C(N)=N1 UBUFOHLVTQZEQF-UHFFFAOYSA-N 0.000 claims description 2
MIROPXUFDXCYLG-UHFFFAOYSA-N pyridine-2,5-diamine Chemical compound NC1=CC=C(N)N=C1 MIROPXUFDXCYLG-UHFFFAOYSA-N 0.000 claims description 2
VHNQIURBCCNWDN-UHFFFAOYSA-N pyridine-2,6-diamine Chemical compound NC1=CC=CC(N)=N1 VHNQIURBCCNWDN-UHFFFAOYSA-N 0.000 claims description 2
WLFXSECCHULRRO-UHFFFAOYSA-N pyridine-2,6-diol Chemical compound OC1=CC=CC(O)=N1 WLFXSECCHULRRO-UHFFFAOYSA-N 0.000 claims description 2
229940083082 pyrimidine derivative acting on arteriolar smooth muscle Drugs 0.000 claims description 2
150000003230 pyrimidines Chemical class 0.000 claims description 2
239000003352 sequestering agent Substances 0.000 claims description 2
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 claims 2
NKNCGBHPGCHYCQ-UHFFFAOYSA-N (2,5-diaminophenyl)methanol Chemical compound NC1=CC=C(N)C(CO)=C1 NKNCGBHPGCHYCQ-UHFFFAOYSA-N 0.000 claims 1
SKYBRLALUDNCSM-UHFFFAOYSA-N 1,1-dimethyl-2-phenylhydrazine Chemical compound CN(C)NC1=CC=CC=C1 SKYBRLALUDNCSM-UHFFFAOYSA-N 0.000 claims 1
YBQZXXMEJHZYMB-UHFFFAOYSA-N 1,2-diphenylhydrazine Chemical compound C=1C=CC=CC=1NNC1=CC=CC=C1 YBQZXXMEJHZYMB-UHFFFAOYSA-N 0.000 claims 1
GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims 1
FRASJONUBLZVQX-UHFFFAOYSA-N 1,4-dioxonaphthalene Natural products C1=CC=C2C(=O)C=CC(=O)C2=C1 FRASJONUBLZVQX-UHFFFAOYSA-N 0.000 claims 1
DTKPVPOLKLGLLG-UHFFFAOYSA-N 1-(2-methoxyethyl)-2-phenylhydrazine Chemical compound COCCNNC1=CC=CC=C1 DTKPVPOLKLGLLG-UHFFFAOYSA-N 0.000 claims 1
GZVVXXLYQIFVCA-UHFFFAOYSA-N 2,3-dimethylbenzene-1,4-diamine Chemical compound CC1=C(C)C(N)=CC=C1N GZVVXXLYQIFVCA-UHFFFAOYSA-N 0.000 claims 1
UEANEAODIZOETQ-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)acetic acid Chemical compound NC1=CC=C(OCC(O)=O)C(N)=C1 UEANEAODIZOETQ-UHFFFAOYSA-N 0.000 claims 1
WCPGNFONICRLCL-UHFFFAOYSA-N 2-(2,4-diaminophenoxy)ethanol Chemical compound NC1=CC=C(OCCO)C(N)=C1 WCPGNFONICRLCL-UHFFFAOYSA-N 0.000 claims 1
HCPJEHJGFKWRFM-UHFFFAOYSA-N 2-amino-5-methylphenol Chemical compound CC1=CC=C(N)C(O)=C1 HCPJEHJGFKWRFM-UHFFFAOYSA-N 0.000 claims 1
WNYJRJRHKRZXEO-UHFFFAOYSA-N 2-propan-2-ylbenzene-1,4-diamine Chemical compound CC(C)C1=CC(N)=CC=C1N WNYJRJRHKRZXEO-UHFFFAOYSA-N 0.000 claims 1
UVUGDGRIYQQKIT-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-amine Chemical compound O1CCNC2=CC(N)=CC=C21 UVUGDGRIYQQKIT-UHFFFAOYSA-N 0.000 claims 1
HWWIVWKTKZAORO-UHFFFAOYSA-N 3,4-dihydro-2h-1,4-benzoxazin-6-ol Chemical compound O1CCNC2=CC(O)=CC=C21 HWWIVWKTKZAORO-UHFFFAOYSA-N 0.000 claims 1
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150000004056 anthraquinones Chemical class 0.000 claims 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 1
FUPMLXVNXBAYIE-UHFFFAOYSA-N n,n-bis(ethylamino)aniline Chemical compound CCNN(NCC)C1=CC=CC=C1 FUPMLXVNXBAYIE-UHFFFAOYSA-N 0.000 claims 1
150000002823 nitrates Chemical class 0.000 claims 1
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238000004040 coloring Methods 0.000 description 6
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239000000243 solution Substances 0.000 description 3
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150000005215 alkyl ethers Chemical class 0.000 description 2
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239000007864 aqueous solution Substances 0.000 description 2
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239000000118 hair dye Substances 0.000 description 2
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241000158728 Meliaceae Species 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 1
CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 1
GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical compound OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
241000589636 Xanthomonas campestris Species 0.000 description 1
239000002535 acidifier Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
239000002671 adjuvant Substances 0.000 description 1
125000003282 alkyl amino group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
125000003277 amino group Chemical group 0.000 description 1
CBTVGIZVANVGBH-UHFFFAOYSA-N aminomethyl propanol Chemical compound CC(C)(N)CO CBTVGIZVANVGBH-UHFFFAOYSA-N 0.000 description 1
239000001099 ammonium carbonate Substances 0.000 description 1
235000012501 ammonium carbonate Nutrition 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
VHFSMDHANDABQK-UHFFFAOYSA-N azane;2-sulfanylpropanoic acid Chemical compound [NH4+].CC(S)C([O-])=O VHFSMDHANDABQK-UHFFFAOYSA-N 0.000 description 1
239000002610 basifying agent Substances 0.000 description 1
WQZGKKKJIJFFOK-VFUOTHLCSA-N beta-D-glucose Chemical compound OC[C@H]1O[C@@H](O)[C@H](O)[C@@H](O)[C@@H]1O WQZGKKKJIJFFOK-VFUOTHLCSA-N 0.000 description 1
239000004202 carbamide Substances 0.000 description 1
210000004534 cecum Anatomy 0.000 description 1
239000003086 colorant Substances 0.000 description 1
229910052802 copper Inorganic materials 0.000 description 1
239000010949 copper Substances 0.000 description 1
239000006071 cream Substances 0.000 description 1
230000001687 destabilization Effects 0.000 description 1
150000004985 diamines Chemical class 0.000 description 1
238000004090 dissolution Methods 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000839 emulsion Substances 0.000 description 1
238000000855 fermentation Methods 0.000 description 1
230000004151 fermentation Effects 0.000 description 1
239000010437 gem Substances 0.000 description 1
239000008103 glucose Substances 0.000 description 1
229940097043 glucuronic acid Drugs 0.000 description 1
229940100608 glycol distearate Drugs 0.000 description 1
229910052736 halogen Inorganic materials 0.000 description 1
125000005843 halogen group Chemical group 0.000 description 1
150000002367 halogens Chemical class 0.000 description 1
150000002391 heterocyclic compounds Chemical class 0.000 description 1
125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 1
238000000034 method Methods 0.000 description 1
244000005700 microbiome Species 0.000 description 1
235000013336 milk Nutrition 0.000 description 1
239000008267 milk Substances 0.000 description 1
210000004080 milk Anatomy 0.000 description 1
150000002772 monosaccharides Chemical class 0.000 description 1
NXPPAOGUKPJVDI-UHFFFAOYSA-N naphthalene-1,2-diol Chemical compound C1=CC=CC2=C(O)C(O)=CC=C21 NXPPAOGUKPJVDI-UHFFFAOYSA-N 0.000 description 1
239000001005 nitro dye Substances 0.000 description 1
239000011591 potassium Substances 0.000 description 1
238000004321 preservation Methods 0.000 description 1
230000002335 preservative effect Effects 0.000 description 1
150000003222 pyridines Chemical class 0.000 description 1
125000001453 quaternary ammonium group Chemical group 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
150000003839 salts Chemical class 0.000 description 1
229910052708 sodium Inorganic materials 0.000 description 1
239000011734 sodium Substances 0.000 description 1
229910052938 sodium sulfate Inorganic materials 0.000 description 1
235000011152 sodium sulphate Nutrition 0.000 description 1
239000002562 thickening agent Substances 0.000 description 1
230000002110 toxicologic effect Effects 0.000 description 1
231100000027 toxicology Toxicity 0.000 description 1
238000005406 washing Methods 0.000 description 1

Classifications

- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/415—Aminophenols
- 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
- A61K8/411—Aromatic amines, i.e. where the amino group is directly linked to the aromatic nucleus
- 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
- A61K8/72—Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
- A61K8/73—Polysaccharides
- 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

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)

LU85705A 1984-12-21 1984-12-21 Composition tinctoriale capillaire a base de colorants d'oxydation et de gomme de xanthane LU85705A1 (fr)

Priority Applications (12)

Application Number	Priority Date	Filing Date	Title
LU85705A LU85705A1 (fr)	1984-12-21	1984-12-21	Composition tinctoriale capillaire a base de colorants d'oxydation et de gomme de xanthane
NL8503442A NL8503442A (nl)	1984-12-21	1985-12-13	Capillair verfpreparaat op basis van oxydatiekleurstoffen en bioheteropolysacchariden.
CH5382/85A CH667389A5 (fr)	1984-12-21	1985-12-17	Composition tinctoriale capillaire a base de colorants d'oxydation et de bio-heteropolysaccharides.
FR8518877A FR2575067B1 (fr)	1984-12-21	1985-12-19	Composition tinctoriale capillaire a base de colorants d'oxydation et de bio-heteropolysaccharides
AT0369085A AT396550B (de)	1984-12-21	1985-12-19	Färbemittel für keratinfasern und insbesondere für humanhaare
JP60287605A JPH0657648B2 (ja)	1984-12-21	1985-12-20	染毛組成物
GB08531462A GB2168727B (en)	1984-12-21	1985-12-20	Dyeing composition for keratinous fibres
IT68089/85A IT1193449B (it)	1984-12-21	1985-12-20	Composizione tintoria per capelli a base di coloranti d'ossidazione e di bio-eteropolisaccaridi
DE3545371A DE3545371C2 (de)	1984-12-21	1985-12-20	Färbemittel auf Basis von Oxidationsfarbstoffen und Bio-Heteropolysacchariden sowie seine Verwendung
BE0/216041A BE903916A (fr)	1984-12-21	1985-12-20	Composition tinctoriale capillaire a base de colorants d'oxydation et de bio-heteropolysaccharides.
CA000498372A CA1258634A (fr)	1984-12-21	1985-12-20	Composition tinctoriale capillaire a base de colorants d'oxydation et de bio- heteropolysaccharides
US07/132,652 US4904275A (en)	1984-12-21	1987-12-10	Hair dyeing composition based on oxidation dyes and bio-heteropolysaccharides

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
LU85705A LU85705A1 (fr)	1984-12-21	1984-12-21	Composition tinctoriale capillaire a base de colorants d'oxydation et de gomme de xanthane
LU85705		1984-12-21

Publications (1)

Publication Number	Publication Date
LU85705A1 true LU85705A1 (fr)	1986-07-17

Family

ID=19730379

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
LU85705A LU85705A1 (fr)	1984-12-21	1984-12-21	Composition tinctoriale capillaire a base de colorants d'oxydation et de gomme de xanthane

Country Status (12)

Country	Link
US (1)	US4904275A (it)
JP (1)	JPH0657648B2 (it)
AT (1)	AT396550B (it)
BE (1)	BE903916A (it)
CA (1)	CA1258634A (it)
CH (1)	CH667389A5 (it)
DE (1)	DE3545371C2 (it)
FR (1)	FR2575067B1 (it)
GB (1)	GB2168727B (it)
IT (1)	IT1193449B (it)
LU (1)	LU85705A1 (it)
NL (1)	NL8503442A (it)

Families Citing this family (41)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE3644980A1 (de) *	1986-12-24	1988-07-07	Pav Praezisions Apparatebau Ag	Messkluppe
DE3917304A1 (de) *	1989-05-27	1990-11-29	Wella Ag	Oxidationshaarfaerbemittel
FR2653016B1 (fr) *	1989-10-13	1994-09-16	Oreal	Composition de lavage des matieres keratiniques, en particulier des cheveux et/ou de la peau.
US5034014A (en) *	1990-06-18	1991-07-23	Clairol, Inc.	Hair dye composition and method
US5356439A (en) *	1992-09-14	1994-10-18	Shiseido Co., Ltd.	Non-oxidative permanent dye formulation for hair and synthetic fibers
DE4342009C2 (de) *	1993-12-09	1996-05-23	Goldwell Gmbh	Haarfärbemittel
FR2713924B1 (fr) *	1993-12-22	1996-01-19	Oreal	Procédé de coloration d'oxydation des fibres kératiniques humaines à l'aide de vapeur d'eau.
FR2715298B1 (fr) *	1994-01-24	1996-02-23	Oreal	Composition de teinture d'oxydation des fibres kératiniques comprenant un dérivé de paraphénylènediamine et le 5-amino 2-méthyl phénol, et procédé de teinture utilisant une telle composition.
FR2715296B1 (fr) *	1994-01-24	1996-04-12	Oreal	Composition de teinture d'oxydation des fibres kératiniques comprenant une paraphénylènediamine, une métalphénylènediamine et un para-aminophénol ou un méta-aminophénol, et procédé de teinture utilisant une telle composition.
FR2715295B1 (fr) *	1994-01-24	1996-04-12	Oreal	Composition de teinture d'oxydation des fibres kératiniques comprenant un dérivé de paraphénylènediamine et un dérivé de métaphénylènediamine, et procédé de teinture utilisant une telle composition.
FR2715297B1 (fr) *	1994-01-24	1996-02-23	Oreal	Composition de teinture d'oxydation des fibres kératiniques comprenant un dérivé de paraphénylènediamine et un dérivé de métaaminophénol, et procédé de teinture utilisant une telle composition.
FR2720275B1 (fr) *	1994-05-26	1996-07-05	Oreal	Composition de teinture d'oxydation des fibres kératiniques comprenant un dérivé de paraphénylènediamine et une 6-hydroxy 1,4-benzoxazine, et procédé de teinture utilisant une telle composition .
FR2720633B1 (fr) *	1994-06-06	1996-07-05	Oreal	Composition de teinture d'oxydation des fibres kératiniques comprenant la 2-(BETHA-hydroxyéthyl) paraphénylènediamine, la 2-méthylrésorcine et le 3-aminophénol, et procédé de teinture utilisant une telle composition.
FR2726185B1 (fr) *	1994-11-02	1997-04-25	Oreal	Composition tinctoriale a base de colorants d'oxydation et procede de teinture mettant en oeuvre cette composition
DE4440957A1 (de)	1994-11-17	1996-05-23	Henkel Kgaa	Oxidationsfärbemittel
DE19505634C2 (de) *	1995-02-18	1998-04-16	Wella Ag	Mittel und Verfahren zum oxidativen Färben von Haaren
CN1129419C (zh) *	1996-01-22	2003-12-03	花王株式会社	美发品组合物
FR2751533B1 (fr)	1996-07-23	2003-08-15	Oreal	Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile non-ionique
FR2753093B1 (fr)	1996-09-06	1998-10-16	Oreal	Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile anionique
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
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
FR2773475B1 (fr) *	1998-01-13	2001-02-02	Oreal	Composition tinctoriale et procedes de teinture des fibres keratiniques la mettant en oeuvre
FR2773472B1 (fr) *	1998-01-13	2002-10-11	Oreal	Composition tictoriale et procedes de teinture des fibres keratiniques la mettant en oeuvre
FR2773480B1 (fr) *	1998-01-13	2000-05-12	Oreal	Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition
US6074438A (en) *	1998-03-03	2000-06-13	Bristol-Myers Squibb Co.	Hair dyeing compositions containing 2-chloro- and 2,6-dichloro-4-aminophenol and phenylpyrazolones
GB2348707B (en)	1999-04-07	2003-07-09	Healthcare Technology Ltd	Heart activity detection apparatus
DE19936442A1 (de)	1999-08-03	2001-02-08	Henkel Kgaa	Neue Entwickler-Kuppler-Kombinationen
FR2807646B1 (fr) *	2000-04-12	2006-12-01	Oreal	Composition de teinture des fibres keratiniques et procede de teinture mettant en oeuvre cette composition
FR2807649B1 (fr) *	2000-04-12	2005-05-06	Oreal	Composition pour la teinture d'oxydation des fibres keratiniques comprenant un derive de la 3,5-diamino- pyridine et un polymere epaississant particulier
FR2807647B1 (fr)	2000-04-12	2005-08-26	Oreal	Composition de teinture d'oxydation des fibres keratiniques et procede mettant en oeuvre cette composition
FR2807648B1 (fr)	2000-04-12	2005-06-10	Oreal	Composition de teinture d'oxydation des fibres keratiniques et procede de teinture mettant en oeuvre cette composition
JP5392882B2 (ja) *	2006-12-08	2014-01-22	株式会社マンダム	毛髪処理剤用キット
JP5158744B2 (ja) *	2006-12-08	2013-03-06	株式会社マンダム	毛髪処理剤用キット
FR2910282B1 (fr) †	2006-12-21	2009-06-05	Oreal	Composition de teinture directe comprenant un tensio-actif cationique, un bioheteropolysaccharide, un tensio-actif amphotere ou non ionique et un colorant direct
FR2910281B1 (fr)	2006-12-21	2009-10-16	Oreal	Composition de teinture d'oxydation comprenant un tensio-actif cationique, un bioheterooolysacchardie, un tensio-actif amphotere ou non ionique et un precurseur de colorant
WO2010133573A2 (en) *	2009-05-19	2010-11-25	L'oreal	Dyeing composition comprising a secondary para-phenylenediamine oxidation base and a thickening polymer
FR2945729B1 (fr) *	2009-05-19	2012-10-19	Oreal	Composition tinctoriale comprenant une base d'oxydation para-phenylene diamine secondaire et un polymere non associatif non cationique a motifs sucres.
DE102012201338A1 (de)	2012-01-31	2013-08-01	Henkel Ag & Co. Kgaa	Oxidationsmittelzubereitung mit optimierter Viskosität zur Behandlung von keratinischen Fasern
KR101974879B1 (ko) *	2017-07-19	2019-05-07	한국과학기술원	수성 염색제 조성물 및 이를 포함하는 염색용 샴푸
WO2023272588A1 (en) *	2021-06-30	2023-01-05	L'oreal	Retardant composition of oxidation
FR3130151B1 (fr) *	2021-12-10	2024-04-05	Oreal	Composition comprenant un précurseur de coloration d’oxydation particulier, un alcool gras oxyalkyléné et un polysaccharide.

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
BE786710A (fr) *	1971-10-04	1973-01-25	Bristol Myers Co	Composition pour la teinture du cheveu avec
CA1025881A (en) *	1973-10-15	1978-02-07	Alexander Halasz	Dyeing keratin fibers with 2-substituted m-toluenediamines
FR2459042A1 (fr) *	1979-06-18	1981-01-09	Oreal	Nouvelles compositions tinctoriales pour cheveux contenant, comme coupleur le diamino-2,4 butoxybenzene et/ou ses sels
FR2510404A1 (fr) *	1981-08-03	1983-02-04	Fabre Sa Pierre	Preparation cosmetique extemporanee a pouvoir colorant, en particulier a usage capillaire
JPS59108710A (ja) *	1982-12-13	1984-06-23	Kao Corp	毛髪化粧料
LU84708A1 (fr) *	1983-03-23	1984-11-14	Oreal	Composition epaissie ou gelifiee de conditionnement des cheveux contenant au moins un polymere cationique,au moins un polymere anionique et au moins une gomme de xanthane
FR2547300B1 (fr) *	1983-06-13	1986-04-18	Oreal	Nouveaux metaaminophenols substitues, leur procede de preparation, compositions tinctoriales pour cheveux les contenant et procede de teinture de cheveux correspondant
LU84875A1 (fr) *	1983-06-27	1985-03-29	Oreal	Compositions tinctoriales pour fibres keratiniques a base de colorants directs et de gomme de xanthane

1984
- 1984-12-21 LU LU85705A patent/LU85705A1/fr unknown
1985
- 1985-12-13 NL NL8503442A patent/NL8503442A/nl not_active Application Discontinuation
- 1985-12-17 CH CH5382/85A patent/CH667389A5/fr not_active IP Right Cessation
- 1985-12-19 FR FR8518877A patent/FR2575067B1/fr not_active Expired
- 1985-12-19 AT AT0369085A patent/AT396550B/de not_active IP Right Cessation
- 1985-12-20 IT IT68089/85A patent/IT1193449B/it active
- 1985-12-20 JP JP60287605A patent/JPH0657648B2/ja not_active Expired - Lifetime
- 1985-12-20 CA CA000498372A patent/CA1258634A/fr not_active Expired
- 1985-12-20 GB GB08531462A patent/GB2168727B/en not_active Expired
- 1985-12-20 BE BE0/216041A patent/BE903916A/fr not_active IP Right Cessation
- 1985-12-20 DE DE3545371A patent/DE3545371C2/de not_active Revoked
1987
- 1987-12-10 US US07/132,652 patent/US4904275A/en not_active Expired - Lifetime

Also Published As

Publication number	Publication date
AT396550B (de)	1993-10-25
FR2575067A1 (fr)	1986-06-27
NL8503442A (nl)	1986-07-16
DE3545371C2 (de)	1994-08-11
DE3545371A1 (de)	1986-07-03
CH667389A5 (fr)	1988-10-14
US4904275A (en)	1990-02-27
JPH0657648B2 (ja)	1994-08-03
GB2168727A (en)	1986-06-25
FR2575067B1 (fr)	1988-08-26
JPS61152620A (ja)	1986-07-11
GB2168727B (en)	1988-10-12
ATA369085A (de)	1993-02-15
BE903916A (fr)	1986-06-20
GB8531462D0 (en)	1986-02-05
CA1258634A (fr)	1989-08-22
IT1193449B (it)	1988-06-22
IT8568089A0 (it)	1985-12-20

Publication	Publication Date	Title
LU85705A1 (fr)	1986-07-17	Composition tinctoriale capillaire a base de colorants d'oxydation et de gomme de xanthane
CA1141665A (fr)	1983-02-22	Procede de teinture de fibres keratiniques en deux temps
CA2263037C (fr)	2005-07-12	Procede de teinture d'oxydation et composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile cationique
US4985955A (en)	1991-01-22	Process for dyeing keratinous fibres with couplers and/or "rapid" oxidation dyes combined with an iodide and dyeing composition employed
DE69100880T2 (de)	1994-04-07	Verfahren zur keratinischen Färbung mit 4-Hydroxyindol bei säurigem pH-Wert und Mittel.
US4268264A (en)	1981-05-19	Composition for hair dyeing which contains a para base and an ortho base
US4883656A (en)	1989-11-28	Composition and method for the oxidative dyeing of hair
HU224430B1 (hu)	2005-09-28	Keratintartalmú rostok oxidációs festésére való készítmény és festési eljárás a készítmény alkalmazásával
EP0850637A1 (fr)	1998-07-01	Composition de teinture d'oxydation des fibres kératiniques et procédé de teinture mettant en oeuvre cette composition
FR2751533A1 (fr)	1998-01-30	Composition de teinture d'oxydation pour fibres keratiniques comprenant un polymere amphiphile non-ionique
CH642255A5 (fr)	1984-04-13	Procede de teinture des fibres keratiniques en deux temps par variation de ph.
HUP0102869A2 (hu)	2002-02-28	Keratin szálak színezésére szolgáló festőanyag
CH649213A5 (fr)	1985-05-15	Procede de coloration de fibres keratiniques a l'aide de derives hydroxyles du benzaldehyde et composition tinctoriale mettant en oeuvre lesdits derives.
DE3824122A1 (de)	1989-01-26	Verfahren zum faerben keratinischer fasern mit mindestens einem farbstoff der indolreihe
JP2000503327A (ja)	2000-03-21	ケラチン繊維上においてメタメリー効果を発現する染色剤
CH644752A5 (fr)	1984-08-31	Compositions tinctoriales pour cheveux contenant, comme coupleur, le diamino-2,4 butoxybenzene ou ses sels.
LU83177A1 (fr)	1982-09-10	Utilisation d'hydroxyanthraquinones pour la coloration des fibres keratiniques humaines,procede et composition les mettant en oeuvre
FR2492257A1 (fr)	1982-04-23	Compositions tinctoriales a base de precurseurs de colorants d'oxydation et de colorants nitres benzeniques stables en milieu alcalin reducteur et leur utilisation pour la teinture des fibres keratiniques
WO2001026616A1 (de)	2001-04-19	Haarfärbeverfahren
FR2519251A1 (fr)	1983-07-08	Composition tinctoriales a base de precurseurs de colorants d'oxydation et d'orthonitranilines n-substituees comprenant une alcanolamine et du bisulfite de sodium et leur utilisation en teinture des fibres keratiniques
JPH0214323B2 (it)	1990-04-06
CA1028956A (fr)	1978-04-04	Coupleurs halogeno-3 acetylamino (ou ureido)-6 phenols
CA1188880A (fr)	1985-06-18	Utilisation de derives alkyles de l'hydroquinone comme agent anti-oxydant dans des compositions tinctoriales d'oxydation
CA2108638A1 (fr)	1994-05-21	Utilisation du 4-hydroxy- ou 4-aminobenzimidazole ou de leurs derives comme coupleurs dans des compositions tinctoriales d'oxydation, compositions et procedes de mise en oeuvre
CA1158561A (fr)	1983-12-13	Composition tinctoriale pour cheveux a base de paraphenylene diamines