NL8502230A - Verfsamenstelling voor keratinevezels, die ten minste een co-oplosbaar gemaakt n-gesubstitueerd 2-nitro-p-fenyleendiamine bevat en werkwijze voor het verven van keratinevezels. - Google Patents
Verfsamenstelling voor keratinevezels, die ten minste een co-oplosbaar gemaakt n-gesubstitueerd 2-nitro-p-fenyleendiamine bevat en werkwijze voor het verven van keratinevezels. Download PDFInfo
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- NL8502230A NL8502230A NL8502230A NL8502230A NL8502230A NL 8502230 A NL8502230 A NL 8502230A NL 8502230 A NL8502230 A NL 8502230A NL 8502230 A NL8502230 A NL 8502230A NL 8502230 A NL8502230 A NL 8502230A
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- Netherlands
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- composition according
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- composition
- formula
- hydroxyethyl
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- 239000000203 mixture Substances 0.000 title claims description 91
- 239000003973 paint Substances 0.000 title claims description 25
- 239000000835 fiber Substances 0.000 title claims description 18
- 102000011782 Keratins Human genes 0.000 title claims description 15
- 108010076876 Keratins Proteins 0.000 title claims description 15
- 238000004043 dyeing Methods 0.000 title claims description 12
- 238000000034 method Methods 0.000 title claims description 6
- HVHNMNGARPCGGD-UHFFFAOYSA-N 2-nitro-p-phenylenediamine Chemical class NC1=CC=C(N)C([N+]([O-])=O)=C1 HVHNMNGARPCGGD-UHFFFAOYSA-N 0.000 title description 6
- -1 2-nitro-paraphenylene diamines Chemical class 0.000 claims description 33
- 150000001875 compounds Chemical class 0.000 claims description 32
- 239000000975 dye Substances 0.000 claims description 26
- 125000000217 alkyl group Chemical group 0.000 claims description 22
- 125000004432 carbon atom Chemical group C* 0.000 claims description 22
- 125000004435 hydrogen atom Chemical class [H]* 0.000 claims description 20
- 229910052739 hydrogen Inorganic materials 0.000 claims description 15
- 150000003839 salts Chemical group 0.000 claims description 14
- 239000001257 hydrogen Substances 0.000 claims description 12
- ZFXYFBGIUFBOJW-UHFFFAOYSA-N theophylline Chemical compound O=C1N(C)C(=O)N(C)C2=C1NC=N2 ZFXYFBGIUFBOJW-UHFFFAOYSA-N 0.000 claims description 11
- 125000003277 amino group Chemical group 0.000 claims description 10
- RYYVLZVUVIJVGH-UHFFFAOYSA-N caffeine Chemical compound CN1C(=O)N(C)C(=O)C2=C1N=CN2C RYYVLZVUVIJVGH-UHFFFAOYSA-N 0.000 claims description 10
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- POULHZVOKOAJMA-UHFFFAOYSA-N methyl undecanoic acid Natural products CCCCCCCCCCCC(O)=O POULHZVOKOAJMA-UHFFFAOYSA-N 0.000 claims description 8
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 7
- 239000001005 nitro dye Substances 0.000 claims description 7
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- VJEONQKOZGKCAK-UHFFFAOYSA-N caffeine Natural products CN1C(=O)N(C)C(=O)C2=C1C=CN2C VJEONQKOZGKCAK-UHFFFAOYSA-N 0.000 claims description 5
- BOKGTLAJQHTOKE-UHFFFAOYSA-N 1,5-dihydroxynaphthalene Chemical compound C1=CC=C2C(O)=CC=CC2=C1O BOKGTLAJQHTOKE-UHFFFAOYSA-N 0.000 claims description 4
- 235000013162 Cocos nucifera Nutrition 0.000 claims description 4
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- 229910052757 nitrogen Inorganic materials 0.000 claims description 4
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- LEHOTFFKMJEONL-UHFFFAOYSA-N Uric Acid Chemical compound N1C(=O)NC(=O)C2=C1NC(=O)N2 LEHOTFFKMJEONL-UHFFFAOYSA-N 0.000 claims description 2
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- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
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- 239000007800 oxidant agent Substances 0.000 claims description 2
- 125000004043 oxo group Chemical group O=* 0.000 claims description 2
- 239000001301 oxygen Chemical group 0.000 claims description 2
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- KCXFHTAICRTXLI-UHFFFAOYSA-N propane-1-sulfonic acid Chemical group CCCS(O)(=O)=O KCXFHTAICRTXLI-UHFFFAOYSA-N 0.000 claims description 2
- 239000003352 sequestering agent Substances 0.000 claims description 2
- 229940116269 uric acid Drugs 0.000 claims description 2
- GEYOCULIXLDCMW-UHFFFAOYSA-N 1,2-phenylenediamine Chemical compound NC1=CC=CC=C1N GEYOCULIXLDCMW-UHFFFAOYSA-N 0.000 claims 1
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 claims 1
- QZHXKQKKEBXYRG-UHFFFAOYSA-N 4-n-(4-aminophenyl)benzene-1,4-diamine Chemical compound C1=CC(N)=CC=C1NC1=CC=C(N)C=C1 QZHXKQKKEBXYRG-UHFFFAOYSA-N 0.000 claims 1
- 230000000996 additive effect Effects 0.000 claims 1
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- 150000002193 fatty amides Chemical class 0.000 claims 1
- RSAZYXZUJROYKR-UHFFFAOYSA-N indophenol Chemical compound C1=CC(O)=CC=C1N=C1C=CC(=O)C=C1 RSAZYXZUJROYKR-UHFFFAOYSA-N 0.000 claims 1
- 150000002790 naphthalenes Chemical class 0.000 claims 1
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- 238000005406 washing Methods 0.000 claims 1
- PAYRUJLWNCNPSJ-UHFFFAOYSA-N Aniline Chemical compound NC1=CC=CC=C1 PAYRUJLWNCNPSJ-UHFFFAOYSA-N 0.000 description 12
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 6
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- DPJCXCZTLWNFOH-UHFFFAOYSA-N 2-nitroaniline Chemical compound NC1=CC=CC=C1[N+]([O-])=O DPJCXCZTLWNFOH-UHFFFAOYSA-N 0.000 description 3
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- DURPTKYDGMDSBL-UHFFFAOYSA-N 1-butoxybutane Chemical class CCCCOCCCC DURPTKYDGMDSBL-UHFFFAOYSA-N 0.000 description 2
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- WRMNZCZEMHIOCP-UHFFFAOYSA-N 2-phenylethanol Chemical compound OCCC1=CC=CC=C1 WRMNZCZEMHIOCP-UHFFFAOYSA-N 0.000 description 2
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- 235000011167 hydrochloric acid Nutrition 0.000 description 1
- 239000001866 hydroxypropyl methyl cellulose Substances 0.000 description 1
- 235000010979 hydroxypropyl methyl cellulose Nutrition 0.000 description 1
- 229920003088 hydroxypropyl methyl cellulose Polymers 0.000 description 1
- UFVKGYZPFZQRLF-UHFFFAOYSA-N hydroxypropyl methyl cellulose Chemical compound OC1C(O)C(OC)OC(CO)C1OC1C(O)C(O)C(OC2C(C(O)C(OC3C(C(O)C(O)C(CO)O3)O)C(CO)O2)O)C(CO)O1 UFVKGYZPFZQRLF-UHFFFAOYSA-N 0.000 description 1
- 235000014655 lactic acid Nutrition 0.000 description 1
- 229940031957 lauric acid diethanolamide Drugs 0.000 description 1
- 239000006210 lotion Substances 0.000 description 1
- 159000000003 magnesium salts Chemical class 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
- 235000013336 milk Nutrition 0.000 description 1
- 239000008267 milk Substances 0.000 description 1
- 210000004080 milk Anatomy 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- ZTQDYDIRBKMMQB-UHFFFAOYSA-N n-(4-aminophenyl)nitramide Chemical class NC1=CC=C(N[N+]([O-])=O)C=C1 ZTQDYDIRBKMMQB-UHFFFAOYSA-N 0.000 description 1
- WQEPLUUGTLDZJY-UHFFFAOYSA-N n-Pentadecanoic acid Natural products CCCCCCCCCCCCCCC(O)=O WQEPLUUGTLDZJY-UHFFFAOYSA-N 0.000 description 1
- GOQYKNQRPGWPLP-UHFFFAOYSA-N n-heptadecyl alcohol Natural products CCCCCCCCCCCCCCCCCO GOQYKNQRPGWPLP-UHFFFAOYSA-N 0.000 description 1
- BXWNKGSJHAJOGX-UHFFFAOYSA-N n-hexadecyl alcohol Natural products CCCCCCCCCCCCCCCCO BXWNKGSJHAJOGX-UHFFFAOYSA-N 0.000 description 1
- 230000007935 neutral effect Effects 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 235000005985 organic acids Nutrition 0.000 description 1
- 230000001590 oxidative effect Effects 0.000 description 1
- 125000000913 palmityl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 150000002978 peroxides Chemical class 0.000 description 1
- WVDDGKGOMKODPV-ZQBYOMGUSA-N phenyl(114C)methanol Chemical compound O[14CH2]C1=CC=CC=C1 WVDDGKGOMKODPV-ZQBYOMGUSA-N 0.000 description 1
- 229940067107 phenylethyl alcohol Drugs 0.000 description 1
- 235000011007 phosphoric acid Nutrition 0.000 description 1
- 229920000151 polyglycol Polymers 0.000 description 1
- 239000010695 polyglycol Substances 0.000 description 1
- 239000000047 product Substances 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 238000001953 recrystallisation Methods 0.000 description 1
- WBHHMMIMDMUBKC-XLNAKTSKSA-N ricinelaidic acid Chemical compound CCCCCC[C@@H](O)C\C=C\CCCCCCCC(O)=O WBHHMMIMDMUBKC-XLNAKTSKSA-N 0.000 description 1
- 229960003656 ricinoleic acid Drugs 0.000 description 1
- FEUQNCSVHBHROZ-UHFFFAOYSA-N ricinoleic acid Natural products CCCCCCC(O[Si](C)(C)C)CC=CCCCCCCCC(=O)OC FEUQNCSVHBHROZ-UHFFFAOYSA-N 0.000 description 1
- 239000002453 shampoo Substances 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
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229960001922 sodium perborate Drugs 0.000 description 1
- 229940045872 sodium percarbonate Drugs 0.000 description 1
- PFUVRDFDKPNGAV-UHFFFAOYSA-N sodium peroxide Chemical compound [Na+].[Na+].[O-][O-] PFUVRDFDKPNGAV-UHFFFAOYSA-N 0.000 description 1
- YKLJGMBLPUQQOI-UHFFFAOYSA-M sodium;oxidooxy(oxo)borane Chemical compound [Na+].[O-]OB=O YKLJGMBLPUQQOI-UHFFFAOYSA-M 0.000 description 1
- 230000003381 solubilizing effect Effects 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 238000003756 stirring Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 150000003871 sulfonates Chemical class 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- TUNFSRHWOTWDNC-HKGQFRNVSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCC[14C](O)=O TUNFSRHWOTWDNC-HKGQFRNVSA-N 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- AQLJVWUFPCUVLO-UHFFFAOYSA-N urea hydrogen peroxide Chemical compound OO.NC(N)=O AQLJVWUFPCUVLO-UHFFFAOYSA-N 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
- A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
- A61K8/41—Amines
- A61K8/418—Amines containing nitro groups
-
- 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
- A61K8/4953—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 containing pyrimidine ring derivatives, e.g. minoxidil
-
- 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
- A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring
- A61Q5/065—Preparations for temporary colouring the hair, e.g. direct dyes
-
- 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
- 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)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| LU85501A LU85501A1 (fr) | 1984-08-13 | 1984-08-13 | Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procede de teinture de fibres keratiniques correspondant |
| LU85501 | 1984-08-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NL8502230A true NL8502230A (nl) | 1986-03-03 |
Family
ID=19730305
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NL8502230A NL8502230A (nl) | 1984-08-13 | 1985-08-12 | Verfsamenstelling voor keratinevezels, die ten minste een co-oplosbaar gemaakt n-gesubstitueerd 2-nitro-p-fenyleendiamine bevat en werkwijze voor het verven van keratinevezels. |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US4931066A (cs) |
| JP (1) | JPS61118312A (cs) |
| AU (1) | AU581679B2 (cs) |
| BE (1) | BE903055A (cs) |
| BR (1) | BR8503811A (cs) |
| CA (1) | CA1252725A (cs) |
| CH (1) | CH668552A5 (cs) |
| DE (1) | DE3528882C2 (cs) |
| DK (1) | DK365385A (cs) |
| FR (1) | FR2568772B1 (cs) |
| GB (1) | GB2163460B (cs) |
| GR (1) | GR851961B (cs) |
| IT (1) | IT1190551B (cs) |
| LU (1) | LU85501A1 (cs) |
| NL (1) | NL8502230A (cs) |
| ZA (1) | ZA856078B (cs) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| LU85541A1 (fr) * | 1984-09-17 | 1986-04-03 | Oreal | Nouveau colorant nitre benzenique,son procede de preparation et son utilisation en teinture de fibres keratiniques |
| FR2665637B1 (fr) * | 1990-08-13 | 1993-08-06 | Lvmh Rech | Composition cosmetique ou pharmaceutique, contenant un extrait de coleus esquirolii, de coleus scutellarioides, de coleus xanthanthus ou un de leurs melanges. |
| 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 |
| DE69728038T2 (de) * | 1996-04-25 | 2005-02-17 | L'oreal | Verfahren zum Färben von Keratinfasern mit Farbstoffvorprodukten von Oxidationsfarbstoffen und pulverförmigen Direktfarbstoffen |
| JP3439067B2 (ja) * | 1997-04-28 | 2003-08-25 | ヘンケルライオンコスメティックス株式会社 | 安定に可溶化した尿酸と、水溶性高分子物質とを含有する水性化粧料組成物および水性化粧料組成物における尿酸の安定可溶化方法 |
| JP3323109B2 (ja) * | 1997-06-25 | 2002-09-09 | ヘンケルライオンコスメティックス株式会社 | 安定に可溶化した尿酸と、両性界面活性剤とを含有する水性化粧料組成物および水性化粧料組成物における尿酸の安定可溶化方法 |
| FR2787707B1 (fr) * | 1998-12-23 | 2002-09-20 | Oreal | Procede de teinture mettant en oeuvre un derive cationique et un compose choisi parmi un aldehyde, une cetone, une quinone et un derive de la di-imino-isoindoline ou de la 3-amino-isoindolone |
| DE19944528A1 (de) | 1999-09-17 | 2001-03-22 | Henkel Kgaa | Neue direktziehende Haarfarbstoffe |
| DE10035735C2 (de) * | 2000-07-22 | 2003-02-20 | Wella Ag | Haartonikum zur Vorbeugung oder Behandlung von Haarausfall |
| WO2004004672A1 (en) * | 2002-07-05 | 2004-01-15 | Unilever N.V. | Hair treatment compositions containing xanthine and alpha hydroxy acid |
| US7135168B2 (en) | 2002-09-10 | 2006-11-14 | Revlon Consumer Products Corporation | Hair color compositions and methods for coloring hair |
| US6835018B2 (en) * | 2002-09-10 | 2004-12-28 | Revlon Consumer Products Corporation | Packaged hair color composition and method for coloring hair |
| US6981814B2 (en) * | 2002-09-10 | 2006-01-03 | Redlon Consumer Products Corporation | Container for storing and dispensing flowable products |
| CN117295483A (zh) * | 2021-04-26 | 2023-12-26 | 花王株式会社 | 用于角蛋白纤维染色的化妆产品 |
| CN117255674A (zh) * | 2021-04-26 | 2023-12-19 | 花王株式会社 | 包含直接染料的染色组合物 |
| TW202308588A (zh) * | 2021-04-26 | 2023-03-01 | 日商花王股份有限公司 | 包含鄰二酚或咪唑啶-2,4-二酮之衍生物之水性氧化性組合物 |
| EP4329717A1 (en) * | 2021-04-26 | 2024-03-06 | Kao Corporation | Cosmetic product for dyeing keratin fibers |
Family Cites Families (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AT200263B (de) * | 1953-06-01 | 1958-10-25 | Unilever Nv | Mittel zum Färben von tierischen Fasern, insbesondere von menschlichem Haar |
| FR1310072A (cs) * | 1964-06-12 | 1963-03-04 | ||
| CA1019678A (en) * | 1972-11-24 | 1977-10-25 | George Alperin | Aqueous alkaline hair dye compositions |
| FR2519251B1 (fr) * | 1982-01-05 | 1985-11-22 | Oreal | 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 |
| LU85098A1 (fr) * | 1983-11-21 | 1985-07-17 | Oreal | Composition tinotoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylenediamine n-substituee cosolubilisee et procedes de teinture de fibres keratiniques correspondants |
| LU85421A1 (fr) * | 1984-06-20 | 1986-01-24 | Oreal | Composition tinctoriale pour fibres keratiniques renfermant au moins une nitro-2 paraphenylene n-substituee cosolubilisee et procedes de teinture de fibres keratiniques correspondants |
-
1984
- 1984-08-13 LU LU85501A patent/LU85501A1/fr unknown
-
1985
- 1985-08-09 GR GR851961A patent/GR851961B/el unknown
- 1985-08-09 FR FR8512208A patent/FR2568772B1/fr not_active Expired
- 1985-08-09 US US06/764,074 patent/US4931066A/en not_active Expired - Fee Related
- 1985-08-12 IT IT67724/85A patent/IT1190551B/it active
- 1985-08-12 ZA ZA856078A patent/ZA856078B/xx unknown
- 1985-08-12 CA CA000488509A patent/CA1252725A/fr not_active Expired
- 1985-08-12 AU AU46112/85A patent/AU581679B2/en not_active Ceased
- 1985-08-12 NL NL8502230A patent/NL8502230A/nl not_active Application Discontinuation
- 1985-08-12 DK DK365385A patent/DK365385A/da not_active Application Discontinuation
- 1985-08-12 BR BR8503811A patent/BR8503811A/pt unknown
- 1985-08-12 GB GB08520199A patent/GB2163460B/en not_active Expired
- 1985-08-12 DE DE3528882A patent/DE3528882C2/de not_active Expired - Fee Related
- 1985-08-13 CH CH3479/85A patent/CH668552A5/fr not_active IP Right Cessation
- 1985-08-13 JP JP60178463A patent/JPS61118312A/ja active Pending
- 1985-08-13 BE BE0/215461A patent/BE903055A/fr not_active IP Right Cessation
Also Published As
| Publication number | Publication date |
|---|---|
| GB8520199D0 (en) | 1985-09-18 |
| DK365385A (da) | 1986-02-14 |
| AU4611285A (en) | 1986-02-20 |
| DE3528882C2 (de) | 1996-04-04 |
| FR2568772A1 (fr) | 1986-02-14 |
| CH668552A5 (fr) | 1989-01-13 |
| DK365385D0 (da) | 1985-08-12 |
| DE3528882A1 (de) | 1986-02-20 |
| IT8567724A0 (it) | 1985-08-12 |
| IT1190551B (it) | 1988-02-16 |
| JPS61118312A (ja) | 1986-06-05 |
| LU85501A1 (fr) | 1986-03-11 |
| US4931066A (en) | 1990-06-05 |
| FR2568772B1 (fr) | 1987-01-16 |
| GB2163460A (en) | 1986-02-26 |
| CA1252725A (fr) | 1989-04-18 |
| GB2163460B (en) | 1987-11-18 |
| ZA856078B (en) | 1986-04-30 |
| AU581679B2 (en) | 1989-03-02 |
| BR8503811A (pt) | 1986-05-20 |
| GR851961B (cs) | 1985-12-10 |
| BE903055A (fr) | 1986-02-13 |
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| BV | The patent application has lapsed |