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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 material

Info

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
Application number
GB4642261A
Inventor
Raymond Stanley Ma Frohnsdorff
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Gillette Industries Ltd
Original Assignee
Gillette Industries Ltd
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.)
Filing date
Publication date
Application filed by Gillette Industries Ltd filed Critical Gillette Industries Ltd
Priority to GB4642261A priority Critical patent/GB1012793A/en
Publication of GB1012793A publication Critical patent/GB1012793A/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/10Preparations for permanently dyeing the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/41Amines
    • A61K8/415Aminophenols

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.
GB4642261A 1961-12-28 1961-12-28 Improvements in or relating to the dyeing of hair and other keratinous material Expired GB1012793A (en)

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)

* Cited by examiner, † Cited by third party
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

Cited By (9)

* Cited by examiner, † Cited by third party
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

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