GB1012793A - Improvements in or relating to the dyeing of hair and other keratinous material - Google Patents
Improvements in or relating to the dyeing of hair and other keratinous materialInfo
- Publication number
- GB1012793A GB1012793A GB4642261A GB4642261A GB1012793A GB 1012793 A GB1012793 A GB 1012793A GB 4642261 A GB4642261 A GB 4642261A GB 4642261 A GB4642261 A GB 4642261A GB 1012793 A GB1012793 A GB 1012793A
- Authority
- GB
- United Kingdom
- Prior art keywords
- hydroxyl
- amino
- alkyl
- group
- substituted
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired
Links
- 238000004043 dyeing Methods 0.000 title abstract 2
- 239000000463 material Substances 0.000 title abstract 2
- 150000001875 compounds Chemical class 0.000 abstract 13
- 125000003277 amino group Chemical group 0.000 abstract 11
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 10
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 9
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 8
- 239000002253 acid Substances 0.000 abstract 4
- 238000007792 addition Methods 0.000 abstract 4
- RDOXTESZEPMUJZ-UHFFFAOYSA-N anisole Chemical class COC1=CC=CC=C1 RDOXTESZEPMUJZ-UHFFFAOYSA-N 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 4
- 238000006396 nitration reaction Methods 0.000 abstract 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 238000006722 reduction reaction Methods 0.000 abstract 4
- 150000003839 salts Chemical class 0.000 abstract 4
- 238000006640 acetylation reaction Methods 0.000 abstract 3
- -1 alkyl halide hydroxyalkyl halide Chemical class 0.000 abstract 3
- PCAXITAPTVOLGL-UHFFFAOYSA-N 2,3-diaminophenol Chemical compound NC1=CC=CC(O)=C1N PCAXITAPTVOLGL-UHFFFAOYSA-N 0.000 abstract 2
- BFLWXPJTAKXXKT-UHFFFAOYSA-N 3-methoxybenzene-1,2-diamine Chemical compound COC1=CC=CC(N)=C1N BFLWXPJTAKXXKT-UHFFFAOYSA-N 0.000 abstract 2
- PLIKAWJENQZMHA-UHFFFAOYSA-N 4-aminophenol Chemical compound NC1=CC=C(O)C=C1 PLIKAWJENQZMHA-UHFFFAOYSA-N 0.000 abstract 2
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 230000007062 hydrolysis Effects 0.000 abstract 2
- 238000006460 hydrolysis reaction Methods 0.000 abstract 2
- UZKWTJUDCOPSNM-UHFFFAOYSA-N methoxybenzene Substances CCCCOC=C UZKWTJUDCOPSNM-UHFFFAOYSA-N 0.000 abstract 2
- DZQXQAXLDXJEAG-UHFFFAOYSA-N n-(2-hydroxyphenyl)nitramide Chemical compound OC1=CC=CC=C1N[N+]([O-])=O DZQXQAXLDXJEAG-UHFFFAOYSA-N 0.000 abstract 2
- OTTAZJWFJLQKTP-UHFFFAOYSA-N n-(2-methoxyphenyl)nitramide Chemical compound COC1=CC=CC=C1N[N+]([O-])=O OTTAZJWFJLQKTP-UHFFFAOYSA-N 0.000 abstract 2
- 238000002360 preparation method Methods 0.000 abstract 2
- 239000003755 preservative agent Substances 0.000 abstract 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 abstract 2
- 239000004094 surface-active agent Substances 0.000 abstract 2
- CDAWCLOXVUBKRW-UHFFFAOYSA-N 2-aminophenol Chemical compound NC1=CC=CC=C1O CDAWCLOXVUBKRW-UHFFFAOYSA-N 0.000 abstract 1
- QBGLHYQUZJDZOO-UHFFFAOYSA-N 2-chloro-3-nitrophenol Chemical class OC1=CC=CC([N+]([O-])=O)=C1Cl QBGLHYQUZJDZOO-UHFFFAOYSA-N 0.000 abstract 1
- 235000013162 Cocos nucifera Nutrition 0.000 abstract 1
- 244000060011 Cocos nucifera Species 0.000 abstract 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical class C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 abstract 1
- 238000007126 N-alkylation reaction Methods 0.000 abstract 1
- DBMJMQXJHONAFJ-UHFFFAOYSA-M Sodium laurylsulphate Chemical compound [Na+].CCCCCCCCCCCCOS([O-])(=O)=O DBMJMQXJHONAFJ-UHFFFAOYSA-M 0.000 abstract 1
- 239000004141 Sodium laurylsulphate Substances 0.000 abstract 1
- 230000010933 acylation Effects 0.000 abstract 1
- 238000005917 acylation reaction Methods 0.000 abstract 1
- 150000003973 alkyl amines Chemical class 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 150000001408 amides Chemical class 0.000 abstract 1
- 125000004103 aminoalkyl group Chemical group 0.000 abstract 1
- 239000003963 antioxidant agent Substances 0.000 abstract 1
- 230000003078 antioxidant effect Effects 0.000 abstract 1
- 239000007864 aqueous solution Substances 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- HVHSWFRODXRTOQ-UHFFFAOYSA-N azanium;1,2-dimethyl-3-octadecylbenzene;chloride Chemical compound [NH4+].[Cl-].CCCCCCCCCCCCCCCCCCC1=CC=CC(C)=C1C HVHSWFRODXRTOQ-UHFFFAOYSA-N 0.000 abstract 1
- 229910021538 borax Inorganic materials 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 abstract 1
- 235000014113 dietary fatty acids Nutrition 0.000 abstract 1
- JZKFHQMONDVVNF-UHFFFAOYSA-N dodecyl sulfate;tris(2-hydroxyethyl)azanium Chemical compound OCCN(CCO)CCO.CCCCCCCCCCCCOS(O)(=O)=O JZKFHQMONDVVNF-UHFFFAOYSA-N 0.000 abstract 1
- 238000010931 ester hydrolysis Methods 0.000 abstract 1
- 239000000194 fatty acid Substances 0.000 abstract 1
- 229930195729 fatty acid Natural products 0.000 abstract 1
- 150000004665 fatty acids Chemical class 0.000 abstract 1
- 150000002191 fatty alcohols Chemical class 0.000 abstract 1
- LHGVFZTZFXWLCP-UHFFFAOYSA-N guaiacol Chemical compound COC1=CC=CC=C1O LHGVFZTZFXWLCP-UHFFFAOYSA-N 0.000 abstract 1
- 229910052736 halogen Chemical group 0.000 abstract 1
- 230000026030 halogenation Effects 0.000 abstract 1
- 238000005658 halogenation reaction Methods 0.000 abstract 1
- 150000002367 halogens Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002768 hydroxyalkyl group Chemical group 0.000 abstract 1
- 238000007069 methylation reaction Methods 0.000 abstract 1
- 239000002304 perfume Substances 0.000 abstract 1
- 150000002989 phenols Chemical class 0.000 abstract 1
- 230000002335 preservative effect Effects 0.000 abstract 1
- 235000019333 sodium laurylsulphate Nutrition 0.000 abstract 1
- 235000010265 sodium sulphite Nutrition 0.000 abstract 1
- 235000010339 sodium tetraborate Nutrition 0.000 abstract 1
- 239000002904 solvent Substances 0.000 abstract 1
- 239000003381 stabilizer Substances 0.000 abstract 1
- 238000010561 standard procedure Methods 0.000 abstract 1
- 239000007858 starting material Substances 0.000 abstract 1
- 239000002562 thickening agent Substances 0.000 abstract 1
- BSVBQGMMJUBVOD-UHFFFAOYSA-N trisodium borate Chemical compound [Na+].[Na+].[Na+].[O-]B([O-])[O-] BSVBQGMMJUBVOD-UHFFFAOYSA-N 0.000 abstract 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
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)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
Abstract
The invention comprises (a) compounds of the formula <FORM:1012793/C2/1> where R1 is a C1-3 alkyl, or a hydroxyl- or amino-substituted C1-3 alkyl group, A is a hydroxyl or methoxy group when B is an amino group or A is an amino group when B is a hydroxyl or methoxy group, and X, which is in the 5- or 6-position, is a hydrogen or halogen atom, or a C1-3 alkyl, hydroxyl- or amino-substituted C1-3 alkyl, amino or hydroxyl group, and acid addition salts thereof, (b) compounds of the formula: <FORM:1012793/C2/2> where A1 is a methoxy group when B1 is an amino group and A1 is an amino group when B1 is a methoxy group and X1, which may be substituted in the 5- or 6-position, is a halogen atom or a C1-3 alkyl, hydroxyl- or amino-substituted C1-3 alkyl, amino or hydroxyl group, and acid addition salts thereof, and (c) compounds of the formula: <FORM:1012793/C2/3> where A is an amino group when B is a hydroxyl or methoxy group and A is a hydroxyl or methoxy group when B is an amino group and X1, which may be substituted in the 5- or 6-position, is a halogen atom or a C1-3 alkyl or hydroxyl- or amino-substituted C1-3 alkyl group, and acid additions salts thereof. The compounds are prepared by standard procedures from readily available starting materials. Thus, compounds of Formula (III) can be obtained from the corresponding X1-substituted phenol by nitration and reduction to give the corresponding ortho- or para-aminophenol which is then acetylated, nitrated, reduced and hydrolysed to give the diamino-phenol. Compounds of Formula (II) where X1 = alkyl, hydroxyalkyl, aminoalkyl or halogen can be prepared by O-methylation of the corresponding compound (III) if the other groups are protected by acylation. Alternatively they can be obtained from the corresponding X1-substituted anisole by the sequence described above for the diaminophenol of Formula (III). Compounds of Formula (II), where X1 is hydroxy can be obtained by stepwise O-acetylation, nitration, ester hydrolysis, reduction, N-acetylation, nitration, amide hydrolysis and reduction of the corresponding methoxyphenol. Compounds of Formula (II) where X1 is amino may be prepared by N-acetylation followed by nitration, hydrolysis and reduction of the appropriate diaminoanisole. The compounds of Formula (I) can be obtained from the corresponding nitroaminophenol or nitroaminoanisole by N-alkylation with an alkyl halide hydroxyalkyl halide, epoxyalkane, alkeneimine or aminoalkyl halide or from the appropriate X1-substituted nitrochlorophenol or anisole by reaction with a primary alkylamine or hydroxyalkylamine. The resulting R1-substituted nitroaminophenols or nitroaminoanisoles can then be reduced to the compounds of Formula (I). Some of the halogeno diaminophenols and diaminoanisoles can also be prepared by direct nuclear halogenation of the appropriate compound or its aryl derivative.ALSO:Preparations for use in dyeing hair and other keratinous material comprise an aqueous solution of one or more compounds of the formula: <FORM:1012793/D1-D2/1> where R is a hydrogen atom or a C1-3 alkyl or a hydroxyl- or amino-substituted C1-3 alkyl group, A is a hydroxyl or methoxy group when B is an amino group or A is an amino group when B is a hydroxyl or methoxy group, and X, which may be in the 5- or 6- position, is a hydrogen or halogen atom, or a C1-3 alkyl, hydroxyl- or amino-substituted C1-3 alkyl, amino or hydroxyl group, or the acid addition salts thereof, and one or more of the following: a surface active agent, a thickner, a solvent, a perfume, a preservative, an antioxidant, and a pH stabilizer. Suitable surface active agents are triethanolamine lauryl sulphate, diethanolamide of cocoanut fatty acids, stearyl dimethyl benzene ammonium chloride, and sodium lauryl sulphate; a suitable thickener is the ethylene oxide derivative of higher fatty alcohols; suitable preservatives sodium sulphite and sodium borate. The preparations can also include dyestuffs of other classes.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB4642261A GB1012793A (en) | 1961-12-28 | 1961-12-28 | Improvements in or relating to the dyeing of hair and other keratinous material |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB4642261A GB1012793A (en) | 1961-12-28 | 1961-12-28 | Improvements in or relating to the dyeing of hair and other keratinous material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| GB1012793A true GB1012793A (en) | 1965-12-08 |
Family
ID=10441208
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| GB4642261A Expired GB1012793A (en) | 1961-12-28 | 1961-12-28 | Improvements in or relating to the dyeing of hair and other keratinous material |
Country Status (1)
| Country | Link |
|---|---|
| GB (1) | GB1012793A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2156527A1 (en) * | 1971-10-04 | 1973-06-01 | Bristol Myers Co | |
| US4125367A (en) | 1976-08-20 | 1978-11-14 | L'oreal | Metaphenylenediamines and dyeing compositions containing the same |
| US4662892A (en) * | 1981-09-03 | 1987-05-05 | Lever Brothers Company | Hair dye composition |
| WO2006023436A1 (en) * | 2004-08-16 | 2006-03-02 | The Procter & Gamble Company | Hair dyeing compositions comprising 2-(amino or substituted amino)-3-5-substituted phenol compounds and use thereof |
| EP1634572A1 (en) * | 2004-08-16 | 2006-03-15 | The Procter and Gamble Company | Hair dyeing compositions comprising 2-(Amino or substituted Amino)-3-5-substituted phenol compounds and use thereof |
| EP1715836A1 (en) * | 2003-11-21 | 2006-11-02 | Henkel Kommanditgesellschaft auf Aktien | Method for dyeing fibres containing keratine |
-
1961
- 1961-12-28 GB GB4642261A patent/GB1012793A/en not_active Expired
Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2156527A1 (en) * | 1971-10-04 | 1973-06-01 | Bristol Myers Co | |
| US4125367A (en) | 1976-08-20 | 1978-11-14 | L'oreal | Metaphenylenediamines and dyeing compositions containing the same |
| US4662892A (en) * | 1981-09-03 | 1987-05-05 | Lever Brothers Company | Hair dye composition |
| EP1715836A1 (en) * | 2003-11-21 | 2006-11-02 | Henkel Kommanditgesellschaft auf Aktien | Method for dyeing fibres containing keratine |
| WO2006023436A1 (en) * | 2004-08-16 | 2006-03-02 | The Procter & Gamble Company | Hair dyeing compositions comprising 2-(amino or substituted amino)-3-5-substituted phenol compounds and use thereof |
| EP1634572A1 (en) * | 2004-08-16 | 2006-03-15 | The Procter and Gamble Company | Hair dyeing compositions comprising 2-(Amino or substituted Amino)-3-5-substituted phenol compounds and use thereof |
| CN100512793C (en) * | 2004-08-16 | 2009-07-15 | 宝洁公司 | Hair dyeing compositions comprising 2- (amino or substituted amino) -3-5-substituted phenol compounds and their use |
| US7695525B2 (en) | 2004-08-16 | 2010-04-13 | The Procter & Gamble Company | Hair dyeing compositions comprising 2-(amino or substituted amino)-3-5-substituted phenol compounds and use thereof |
| AU2005277583B2 (en) * | 2004-08-16 | 2010-07-01 | The Procter & Gamble Company | Hair dyeing compositions comprising 2-(amino or substituted amino)-3-5-substituted phenol compounds and use thereof |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US4348202A (en) | Hair dye or bleach supports | |
| US5104413A (en) | Hair dye composition | |
| US3728447A (en) | Fatty acid lactylates and glycolates for conditioning hair | |
| US4314808A (en) | Dye polymers, their preparation and their use in dye compositions | |
| CA2292670C (en) | Direct hair dye compositions and methods containing novel anthraquinone mixtures | |
| GB2186587A (en) | Halogenated 2-nitroanilines and 2-nitro-meta-phenylenediamines for dyeing keratinous fibres | |
| US4132678A (en) | Transparent liquid shampoo | |
| GB2132627A (en) | Hair cosmetic compositions | |
| EP0544400B1 (en) | P-Phenylenediamine substituted by a quaternary ammonium group and an electron withdrawing group | |
| GB1058331A (en) | Amino acid surface-active compounds and their use in hair treatment compositions | |
| JPH0737370B2 (en) | Hair dye composition | |
| ES2054902T3 (en) | 3-SUBSTITUTED PARA-AMINOPHENOLS, THEIR PREPARATION PROCEDURE, THEIR USE IN THE STAINING OF KERATIN FIBERS AND INTERMEDIATE COMPOUNDS USED IN THE PREPARATION PROCEDURE. | |
| GB1012793A (en) | Improvements in or relating to the dyeing of hair and other keratinous material | |
| US4153681A (en) | Composition for permanent waving | |
| US5833969A (en) | Aqueous cosmetic composition containing stably solubilized uric acid and amphoteric surfactant and method for stably solubilizing uric acid in aqueous cosmetic composition | |
| GB1223270A (en) | Improvements in dyeing hair | |
| JP3025537B2 (en) | Hair cosmetics | |
| US4601726A (en) | Dye composition for the direct dyeing of keratinic fibres, containing at least one N-substituted cosolubilized 2-nitroparaphenylenediamine and corresponding processes for dyeing keratinic fibres | |
| GB1531605A (en) | Dyeing compositions for human hair and ethers present in these compositions | |
| FI56769C (en) | HAORBEHANDLINGSMEDEL INNEHAOLLANDE NITRODIPHENYLAMINHAORFAERG | |
| US3819827A (en) | Aluminum oxide containing hair treating composition | |
| US4749379A (en) | Nitroaminophenols and their use in dyeing keratinous fibres. | |
| US4981486A (en) | Nitro benzene dye, the process for preparation thereof and its use in dyeing keratinous fibres | |
| JPS5949204B2 (en) | Hair dyeing and conditioning composition | |
| GB1598567A (en) | Hair preparation |