NL8801811A - Werkwijze voor het verven van keratinevezels, in het bijzonder menselijk haar, met indoolkleurstoffen. - Google Patents
Werkwijze voor het verven van keratinevezels, in het bijzonder menselijk haar, met indoolkleurstoffen. Download PDFInfo
- Publication number
- NL8801811A NL8801811A NL8801811A NL8801811A NL8801811A NL 8801811 A NL8801811 A NL 8801811A NL 8801811 A NL8801811 A NL 8801811A NL 8801811 A NL8801811 A NL 8801811A NL 8801811 A NL8801811 A NL 8801811A
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- Netherlands
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- composition
- process according
- hydrogen atom
- dyes
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- 238000000034 method Methods 0.000 title claims description 50
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- 238000004043 dyeing Methods 0.000 title claims description 26
- 239000000835 fiber Substances 0.000 title claims description 22
- 102000011782 Keratins Human genes 0.000 title claims description 14
- 108010076876 Keratins Proteins 0.000 title claims description 14
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- -1 iodide ions Chemical class 0.000 claims description 39
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- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine Natural products C1=CC=C2CC=NC2=C1 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 claims description 26
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 26
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- HDGMAACKJSBLMW-UHFFFAOYSA-N 4-amino-2-methylphenol Chemical compound CC1=CC(N)=CC=C1O HDGMAACKJSBLMW-UHFFFAOYSA-N 0.000 description 1
- URNPJAGSKRJTAK-UHFFFAOYSA-N 4-amino-3-methylsulfanylphenol Chemical compound CSC1=CC(O)=CC=C1N URNPJAGSKRJTAK-UHFFFAOYSA-N 0.000 description 1
- ROCVGJLXIARCAC-UHFFFAOYSA-N 4-aminobenzene-1,3-diol Chemical compound NC1=CC=C(O)C=C1O ROCVGJLXIARCAC-UHFFFAOYSA-N 0.000 description 1
- YFTGOBNOJKXZJC-UHFFFAOYSA-N 5,6-dihydroxyindole-2-carboxylic acid Chemical compound OC1=C(O)C=C2NC(C(=O)O)=CC2=C1 YFTGOBNOJKXZJC-UHFFFAOYSA-N 0.000 description 1
- RQUKKBGMYZRPEL-UHFFFAOYSA-N 5-(2-hydroxyethylamino)-2-methoxyphenol Chemical compound COC1=CC=C(NCCO)C=C1O RQUKKBGMYZRPEL-UHFFFAOYSA-N 0.000 description 1
- CQPLGGXOAHSQBD-UHFFFAOYSA-N 5-amino-2,4-dimethoxyphenol Chemical compound COC1=CC(OC)=C(O)C=C1N CQPLGGXOAHSQBD-UHFFFAOYSA-N 0.000 description 1
- BLQFHJKRTDIZLX-UHFFFAOYSA-N 5-amino-2-methoxyphenol Chemical compound COC1=CC=C(N)C=C1O BLQFHJKRTDIZLX-UHFFFAOYSA-N 0.000 description 1
- DBFYESDCPWWCHN-UHFFFAOYSA-N 5-amino-2-methylphenol Chemical compound CC1=CC=C(N)C=C1O DBFYESDCPWWCHN-UHFFFAOYSA-N 0.000 description 1
- BKYQHRSVSLQLLQ-UHFFFAOYSA-N 6-methoxy-1,3-benzodioxol-5-amine Chemical compound C1=C(N)C(OC)=CC2=C1OCO2 BKYQHRSVSLQLLQ-UHFFFAOYSA-N 0.000 description 1
- YFVGAKMITMMATA-UHFFFAOYSA-N 6-methoxy-1,3-benzodioxol-5-ol Chemical compound C1=C(O)C(OC)=CC2=C1OCO2 YFVGAKMITMMATA-UHFFFAOYSA-N 0.000 description 1
- ATCBPVDYYNJHSG-UHFFFAOYSA-N 6-methoxy-2-n-methylpyridine-2,3-diamine Chemical compound CNC1=NC(OC)=CC=C1N ATCBPVDYYNJHSG-UHFFFAOYSA-N 0.000 description 1
- SBZBDWBZQAABFX-UHFFFAOYSA-N 7-(2-amino-2-carboxyethyl)-2-[7-(2-amino-2-carboxyethyl)-5-oxo-1,4-benzothiazin-2-yl]-5-hydroxy-4H-1,4-benzothiazine-3-carboxylic acid Chemical compound NC(Cc1cc(O)c2NC(C(O)=O)=C(Sc2c1)c1cnc2c(cc(CC(N)C(O)=O)cc2=O)s1)C(O)=O SBZBDWBZQAABFX-UHFFFAOYSA-N 0.000 description 1
- ZCYVEMRRCGMTRW-UHFFFAOYSA-N 7553-56-2 Chemical compound [I] ZCYVEMRRCGMTRW-UHFFFAOYSA-N 0.000 description 1
- KVHHMYZBFBSVDI-UHFFFAOYSA-N 8-aminonaphthalen-2-ol Chemical compound C1=C(O)C=C2C(N)=CC=CC2=C1 KVHHMYZBFBSVDI-UHFFFAOYSA-N 0.000 description 1
- QSBYPNXLFMSGKH-UHFFFAOYSA-N 9-Heptadecensaeure Natural products CCCCCCCC=CCCCCCCCC(O)=O QSBYPNXLFMSGKH-UHFFFAOYSA-N 0.000 description 1
- GJCOSYZMQJWQCA-UHFFFAOYSA-N 9H-xanthene Chemical compound C1=CC=C2CC3=CC=CC=C3OC2=C1 GJCOSYZMQJWQCA-UHFFFAOYSA-N 0.000 description 1
- VHUUQVKOLVNVRT-UHFFFAOYSA-N Ammonium hydroxide Chemical class [NH4+].[OH-] VHUUQVKOLVNVRT-UHFFFAOYSA-N 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- 244000265919 Chrysolepis chrysophylla Species 0.000 description 1
- 235000000623 Chrysolepis chrysophylla Nutrition 0.000 description 1
- 244000060011 Cocos nucifera Species 0.000 description 1
- 235000013162 Cocos nucifera Nutrition 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 239000005639 Lauric acid Substances 0.000 description 1
- 239000005642 Oleic acid Substances 0.000 description 1
- ZQPPMHVWECSIRJ-UHFFFAOYSA-N Oleic acid Natural products CCCCCCCCC=CCCCCCCCC(O)=O ZQPPMHVWECSIRJ-UHFFFAOYSA-N 0.000 description 1
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 1
- 229920002305 Schizophyllan Polymers 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 1
- 235000011054 acetic acid Nutrition 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000004480 active ingredient Substances 0.000 description 1
- 239000000443 aerosol Substances 0.000 description 1
- 230000003113 alkalizing effect Effects 0.000 description 1
- 125000003342 alkenyl group Chemical group 0.000 description 1
- 150000003973 alkyl amines Chemical class 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 150000001408 amides Chemical class 0.000 description 1
- XIWMTQIUUWJNRP-UHFFFAOYSA-N amidol Chemical compound NC1=CC=C(O)C(N)=C1 XIWMTQIUUWJNRP-UHFFFAOYSA-N 0.000 description 1
- 150000001413 amino acids Chemical class 0.000 description 1
- 125000004103 aminoalkyl group Chemical group 0.000 description 1
- 235000011162 ammonium carbonates Nutrition 0.000 description 1
- 235000011114 ammonium hydroxide Nutrition 0.000 description 1
- 150000004056 anthraquinones Chemical class 0.000 description 1
- 239000012736 aqueous medium Substances 0.000 description 1
- 239000012298 atmosphere Substances 0.000 description 1
- 125000004429 atom Chemical group 0.000 description 1
- 230000003796 beauty Effects 0.000 description 1
- 239000000440 bentonite Substances 0.000 description 1
- 229910000278 bentonite Inorganic materials 0.000 description 1
- SVPXDRXYRYOSEX-UHFFFAOYSA-N bentoquatam Chemical compound O.O=[Si]=O.O=[Al]O[Al]=O SVPXDRXYRYOSEX-UHFFFAOYSA-N 0.000 description 1
- 150000004054 benzoquinones Chemical class 0.000 description 1
- 229920001222 biopolymer Polymers 0.000 description 1
- 230000015572 biosynthetic process Effects 0.000 description 1
- 239000007844 bleaching agent Substances 0.000 description 1
- 239000004202 carbamide Substances 0.000 description 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 description 1
- 150000004649 carbonic acid derivatives Chemical class 0.000 description 1
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 1
- 239000001913 cellulose Substances 0.000 description 1
- 229920002678 cellulose Polymers 0.000 description 1
- 235000015165 citric acid Nutrition 0.000 description 1
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid group Chemical class C(CC(O)(C(=O)O)CC(=O)O)(=O)O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 1
- 238000009833 condensation Methods 0.000 description 1
- 230000005494 condensation Effects 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 230000008034 disappearance Effects 0.000 description 1
- 239000006185 dispersion Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 description 1
- 125000002425 furfuryl group Chemical group C(C1=CC=CO1)* 0.000 description 1
- 235000011167 hydrochloric acid Nutrition 0.000 description 1
- MMBMIVSDYYPRHH-UHFFFAOYSA-N hydrogen peroxide Chemical compound OO.OO MMBMIVSDYYPRHH-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 description 1
- GGNQRNBDZQJCCN-UHFFFAOYSA-N hydroxyhydroquinone Natural products OC1=CC=C(O)C(O)=C1 GGNQRNBDZQJCCN-UHFFFAOYSA-N 0.000 description 1
- 239000011630 iodine Substances 0.000 description 1
- 229910052740 iodine Inorganic materials 0.000 description 1
- QXJSBBXBKPUZAA-UHFFFAOYSA-N isooleic acid Natural products CCCCCCCC=CCCCCCCCCC(O)=O QXJSBBXBKPUZAA-UHFFFAOYSA-N 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 210000002752 melanocyte Anatomy 0.000 description 1
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 1
- 229920000609 methyl cellulose Polymers 0.000 description 1
- 239000001923 methylcellulose Substances 0.000 description 1
- 235000010981 methylcellulose Nutrition 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- XOOMNEFVDUTJPP-UHFFFAOYSA-N naphthalene-1,3-diol Chemical compound C1=CC=CC2=CC(O)=CC(O)=C21 XOOMNEFVDUTJPP-UHFFFAOYSA-N 0.000 description 1
- 150000005181 nitrobenzenes Chemical class 0.000 description 1
- ZQPPMHVWECSIRJ-KTKRTIGZSA-N oleic acid Chemical compound CCCCCCCC\C=C/CCCCCCCC(O)=O ZQPPMHVWECSIRJ-KTKRTIGZSA-N 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920003023 plastic Polymers 0.000 description 1
- 239000004033 plastic Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- MIROPXUFDXCYLG-UHFFFAOYSA-N pyridine-2,5-diamine Chemical compound NC1=CC=C(N)N=C1 MIROPXUFDXCYLG-UHFFFAOYSA-N 0.000 description 1
- 235000010413 sodium alginate Nutrition 0.000 description 1
- 239000000661 sodium alginate Substances 0.000 description 1
- 229940005550 sodium alginate Drugs 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 238000010408 sweeping Methods 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 210000002268 wool Anatomy 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
- A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
- A61K8/20—Halogens; Compounds thereof
-
- 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
- A61K8/4906—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
- A61K8/4913—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid
- A61K8/492—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having five membered rings, e.g. pyrrolidone carboxylic acid having condensed rings, e.g. indol
Landscapes
- 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)
- Chemical & Material Sciences (AREA)
- Inorganic Chemistry (AREA)
- Cosmetics (AREA)
- Coloring (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
LU86947A LU86947A1 (fr) | 1987-07-17 | 1987-07-17 | Procede de teinture des fibres keratiniques,en particulier humaines,avec le 5-(hydroxy ou-methoxy)6-hydroxyindole |
LU86947 | 1987-07-17 |
Publications (1)
Publication Number | Publication Date |
---|---|
NL8801811A true NL8801811A (nl) | 1989-02-16 |
Family
ID=19730950
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NL8801811A NL8801811A (nl) | 1987-07-17 | 1988-07-15 | Werkwijze voor het verven van keratinevezels, in het bijzonder menselijk haar, met indoolkleurstoffen. |
Country Status (11)
Country | Link |
---|---|
JP (1) | JPH0193516A (da) |
BE (1) | BE1002155A5 (da) |
CH (1) | CH676926A5 (da) |
DE (1) | DE3824122A1 (da) |
ES (1) | ES2007267A6 (da) |
FR (1) | FR2618070B1 (da) |
GB (1) | GB2207443B (da) |
IT (1) | IT1223701B (da) |
LU (1) | LU86947A1 (da) |
NL (1) | NL8801811A (da) |
PT (1) | PT87991B (da) |
Families Citing this family (26)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
LU87086A1 (fr) * | 1987-12-18 | 1989-07-07 | Oreal | Procede de teinture des fibres keratiniques avec des colorants d'oxydation associes au 5,6-dihydroxyindole et a un iodure et composition tinctoriale mise en oeuvre |
LU87113A1 (fr) * | 1988-01-26 | 1989-08-30 | Oreal | Procede de teinture des fibres keratiniques et composition de teinture mettant en oeuvre du 5,6-dihydroxyindole,un colorant quinonique et iodure |
LU87128A1 (fr) * | 1988-02-08 | 1989-09-20 | Oreal | Composition de teinture des fibres keratiniques mettant en oeuvre du 5,6-dihydroxyindole et au moins une paraphenylenediamine disubstituee sur l'un des groupements amino et procede de mise en oeuvre |
US5346509A (en) * | 1988-05-12 | 1994-09-13 | Clairol Incorporated | Process for dyeing hair by the sequential treatment of hair with metal ion-containing composition and with a dye composition containing 5,6-dihydroxyindole-2-carboxylic acid and certain derivatives thereof |
LU87256A1 (fr) * | 1988-06-21 | 1990-02-28 | Oreal | Procedes de teinture de fibres keratiniques a base de 5,6-dihydroxyindole et d'au moins un sel de terre rare et compositions de mise en oeuvre |
US5279620A (en) * | 1988-09-12 | 1994-01-18 | L'oreal | Tinctorial compositions for keratin fibres containing precursors of oxidation colorants and indole couplers, and dyeing processes using these compositions |
LU87337A1 (fr) * | 1988-09-12 | 1990-04-06 | Oreal | Compositions tinctoriales pour fibres keratiniques contenant des precurseurs de colorants par oxydation et des coupleurs indoliques et procedes de teinture mettant en oeuvre ces compositions |
FR2649887B1 (fr) * | 1989-07-21 | 1994-07-08 | Oreal | Procede de coloration mettant en oeuvre des colorants indoliques et des precurseurs de colorants d'oxydation et agents de teinture mis en oeuvre |
FR2649886B1 (fr) * | 1989-07-21 | 1991-10-11 | Oreal | Composition de teinture des fibres keratiniques mettant en oeuvre un colorant indolique et au moins une paraphenylenediamine comportant un groupement amino secondaire et procede de mise en oeuvre |
US5167669A (en) * | 1989-07-21 | 1992-12-01 | L'oreal | Composition for dyeing keratinous fibers employing an indole dye and at least one para-phenylenediamine containing a secondary amino group and process for use |
FR2654336B1 (fr) * | 1989-11-10 | 1994-06-03 | Oreal | Composition tinctoriale pour fibres keratiniques, contenant des precurseurs de colorants par oxydation et des coupleurs derives de 6- ou 7-hydroxyindole, et procede de teinture mettant en óoeuvre ces compositions. |
FR2659228B1 (fr) * | 1990-03-08 | 1994-10-14 | Oreal | Procede de teinture des fibres keratiniques avec des 6 ou 7-monohydroxy-indoles a ph acide et compositions mises en óoeuvre. |
US6238439B1 (en) | 1990-06-21 | 2001-05-29 | L'oreal | Method for dyeing keratinous fibers with indole compounds, compositions and devices for implementation |
FR2722687A1 (fr) * | 1994-07-22 | 1996-01-26 | Oreal | Utilisation de gomme de guar dans des compositionsnon rincees pour la teinture des fibres keratiniques et procede de teinture |
ATE261717T1 (de) † | 1997-10-22 | 2004-04-15 | Oreal | Färbemittel für keratinische faser und verfahren zum färben unter verwendung dieser zusammensetzung |
JP4516708B2 (ja) * | 2001-07-12 | 2010-08-04 | ポーラ化成工業株式会社 | 多色毛髪修飾用の化粧料 |
DE102014225553A1 (de) * | 2014-12-11 | 2016-06-16 | Henkel Ag & Co. Kgaa | Mittel und Verfahren zur Behandlung keratinhaltiger Fasern |
DE102014225554A1 (de) | 2014-12-11 | 2016-06-16 | Henkel Ag & Co. Kgaa | Mittel und Verfahren zur Behandlung keratinhaltiger Fasern |
FR3082735B1 (fr) | 2018-06-20 | 2022-03-11 | Oreal | Composition de coloration capillaire comprenant un colorant d’oxydation, une gomme de scleroglucane et un polymere associatif. |
FR3082739B1 (fr) | 2018-06-20 | 2020-05-29 | L'oreal | Procede de coloration capillaire mettant en œuvre une composition colorante et une composition oxydante, lesdites compositions comprenant une gomme de scleroglucane. |
FR3082742B1 (fr) | 2018-06-20 | 2020-05-29 | L'oreal | Composition de coloration capillaire comprenant un colorant d’oxydation, une gomme de scleroglucane, et un alkylpolyglycoside. |
FR3082736B1 (fr) | 2018-06-20 | 2020-05-29 | L'oreal | Composition de coloration capillaire comprenant un colorant d’oxydation, une gomme de scleroglucane et agent alcalin de type acide amine. |
FR3082740B1 (fr) | 2018-06-20 | 2020-05-29 | L'oreal | Composition de coloration capillaire comprenant un colorant d’oxydation, une gomme de scleroglucane, une alcalnolamine et un agent alcalin mineral. |
FR3082738B1 (fr) | 2018-06-20 | 2020-07-10 | L'oreal | Composition de coloration capillaire comprenant un colorant d’oxydation, une gomme de scleroglucane et un polymere cationique. |
FR3082710B1 (fr) | 2018-06-20 | 2021-11-26 | Oreal | Dispositif de distribution d’un produit de coloration capillaire mettant en œuvre une composition colorante et une composition oxydante comprenant une gomme de scleroglucane. |
CN217338168U (zh) * | 2022-01-28 | 2022-09-02 | 宁波飞马行远国际贸易有限公司 | 拼接式树裙 |
Family Cites Families (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BE564450A (da) * | 1957-02-02 | |||
DE1469739A1 (de) * | 1965-10-08 | 1969-01-02 | Bayer Ag | Verfahren zum Faerben von Polyolefinen und Polysiloxanen |
FR2045991A7 (en) * | 1969-06-11 | 1971-03-05 | Gillette Co | Hair tinting preparations with reduced - amounts of peroxide |
LU86256A1 (fr) * | 1986-01-20 | 1988-01-20 | Oreal | Procede de teinture des fibres keratiniques avec du 5,6-dihydroxyindole associe avec un iodure |
LU86668A1 (fr) * | 1986-11-17 | 1988-06-13 | Oreal | Procede de teinture des fibres keratiniques avec des derives d'indole associes avec un iodure |
-
1987
- 1987-07-17 LU LU86947A patent/LU86947A1/fr unknown
-
1988
- 1988-07-12 FR FR8809489A patent/FR2618070B1/fr not_active Expired - Fee Related
- 1988-07-14 CH CH2703/88A patent/CH676926A5/fr not_active IP Right Cessation
- 1988-07-14 PT PT87991A patent/PT87991B/pt not_active IP Right Cessation
- 1988-07-15 BE BE8800829A patent/BE1002155A5/fr not_active IP Right Cessation
- 1988-07-15 DE DE3824122A patent/DE3824122A1/de not_active Withdrawn
- 1988-07-15 NL NL8801811A patent/NL8801811A/nl not_active Application Discontinuation
- 1988-07-16 ES ES8802252A patent/ES2007267A6/es not_active Expired
- 1988-07-18 IT IT67673/88A patent/IT1223701B/it active
- 1988-07-18 JP JP63178913A patent/JPH0193516A/ja active Pending
- 1988-07-18 GB GB8817070A patent/GB2207443B/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
LU86947A1 (fr) | 1989-03-08 |
BE1002155A5 (fr) | 1990-08-14 |
GB2207443A (en) | 1989-02-01 |
GB2207443B (en) | 1991-07-10 |
PT87991A (pt) | 1989-06-30 |
IT8867673A0 (it) | 1988-07-18 |
FR2618070A1 (fr) | 1989-01-20 |
CH676926A5 (da) | 1991-03-28 |
IT1223701B (it) | 1990-09-29 |
DE3824122A1 (de) | 1989-01-26 |
FR2618070B1 (fr) | 1993-11-05 |
PT87991B (pt) | 1995-03-01 |
JPH0193516A (ja) | 1989-04-12 |
ES2007267A6 (es) | 1989-06-01 |
GB8817070D0 (en) | 1988-08-24 |
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