US2733186A - Compositions for the dyeing of hair - Google Patents

Compositions for the dyeing of hair Download PDF

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Publication number
US2733186A
US2733186A US2733186DA US2733186A US 2733186 A US2733186 A US 2733186A US 2733186D A US2733186D A US 2733186DA US 2733186 A US2733186 A US 2733186A
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hair
dyeing
composition
added
parts
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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
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34Alcohols
    • A61K8/347Phenols

Definitions

  • This invention relates to compositions for the dyeing or tinting of hair and to methods of use thereof.
  • Examples of such products are 2-hydroxy-1-4-naphthoquinone and the products desulting from the application of the dyeing process described in French Patent No. 826,046, which process makes it possible to obtain the transformation of trihydroxl derivatives into quinone products on the fibre. In all such cases it is only possible to obtain shades from bloude to titian red on live hair with the aid of these products. Deeper shades can only be obtained by means of these products if they are admixed with products already known for dyeing hair, such as phenylenediamines and aminophenols, which are toxic, or by the addition of metallic salts. This latter process presents the disadvantage of not permitting subsequent capillary treatment, such as permanent waving or bleaching.
  • the present invention provides a composition for the treatment of hair for the purpose of dyeing or tinting which comprises a compound represented by the general formula:
  • X represents a hydrogen or halogen atom, or an alkyl, alkoxy or hydroxy-alkyl group free from solubilising groups.
  • a base or a salt of a base of the group comprising ammonia and primary it is preferred to add to said composition, immediately before carrying out the dyeing of the hair, a base or a salt of a base of the group comprising ammonia and primary,
  • I R represents a bivalent aliphatic residue, which may or may not contain an alcoholic function
  • Y represents a hydrogen atom or a carboxyl group
  • the proportion of reducing agent incorporated in the composition according to the invention permits the speed of development of the shade of dyeing to be regulated, such shade being determined at the time by the nature and relative proportions of the products entering into the final dye obtained after the addition of the base or bases, or a salt of these bases, to this composition at the moment it is used.
  • the mercaptan not only performs the known function of a reducing agent which assists in the maintenance of the original qualities of the trihydroxyl substance which is used, but it also exerts a chemical or physiochemical action which facilitates the formation of the colouring on the hair; however, the invention is not to be regarded as limited by this theory.
  • the invention does not include the addition of metallic salts for any of the shades obtained, it enables the superimposition of dyes and capillary treatments, such as bleaches with persalts and permanent waves to be performed without danger of changing or destroying the hair. This constitutes an essential difference both as regards the process indicated in French Patent No. 826,046 and the publication of Stoves and Burton.
  • the hair dyed in accordance with this novel process is characterised in all cases by a lustre not hitherto obtained by means of ordinary dyes, and as these products are not toxic, they do not necessitate any special precautions being taken, such as a test lock, which it is essential to carry out with dyes having oxidation colouring agents.
  • a composition in accordance with the invention is preferably provided in the form of a cream which facilitates the application to the live head of hair, by using in known manner a thickening agent and an agent having dispersive and wetting properties in order to facilitate the penetration of the dye into the hair.
  • Example I 3 parts of 2-4-5-trihydroxytoluene and 0.4 part of thioglycollic acid are added to the cream obtained by emulsifying 20 parts glycol stearate in 77 parts water by means of a product having dispersive and wetting properties (such as sulphonated lauryl alcohol). At the moment of use, 10 parts of a 20% solution of ammonia are added. The mixture obtained is applied to the hair and left for about half-an-hour at 3540C. The hair is then rinsed, washed and dried.
  • a product having dispersive and wetting properties such as sulphonated lauryl alcohol
  • the hairs are dyed black, the dye being particularly fast to washing, rubbing and light.
  • Example 11 3 parts of 2-4-5-trihydroxytoluene and 0.4 part of thioglycerol are added to a cream obtained by emulsifying 20 parts glycerol stearate in 77 parts water by means of a product having dispersive and wetting properties (such as sulphonated lauryl alcohol). At the moment of use, 2 parts of monoethanolamine are added, the mixture obtained is applied to the hair and left for about half-an-hour at 35-40 C. The hair is rinsed, washed and dried.
  • a product having dispersive and wetting properties such as sulphonated lauryl alcohol
  • the hairs are dyed a deep chestnut brown, the dye being particularly fast to washing, rubbing and light.
  • Example Ill 3 parts of 2-4-5-trihydroxytoluene and 0.4 part of thicglycollic acid are added to a cream obtained by emulsifying 20 parts of glycol stearate in 77 parts water by means of a product having dispersive and Wetting properties (such as sulphonated lauryl alcohol). At the moment of use, parts of triammonium phosphate are added. The mixture obtained is applied to the hair, left for about halfan-hour at 35-40 C., and the hair is rinsed, washed and dried.
  • a product having dispersive and Wetting properties such as sulphonated lauryl alcohol
  • the hair is dyed a deep chestnut brown with a violet glint, the dye being particularly fast to washing, rubbing and light.
  • Example IV 3 parts of 2-4-S-trihydroxytoluene and 0.4 part of thioglycerol are added to a cream obtained by emulsifying parts of glycerol stearate in 77 parts water by means of a product having dispersing and Wetting properties (such as sulphonated lauryl alcohol).
  • a product having dispersing and Wetting properties such as sulphonated lauryl alcohol.
  • 3 parts of triethanolamine are added and the mixture ob tained is applied to the hair. It is left for about half-anhour at 35-40" C. and the hair is then rinsed, washed and dried.
  • the hair is dyed auburn, the dye being particularly fast to washing, rubbing and light.
  • Example V 3 parts of 2-4-5-trihydroxytoluene and 0.4 part of thiolactic acid are added to a cream obtained by emulsifying 20 parts of glycol stearate in 77 parts water, by means of a product having dispersing and wetting properties (such as sulphonated lauryl alcohol). At the moment of use, 2.5 parts of morpholine are added. The mixture obtained is applied to the hair, and left for about half-an-hour at 35-40 C. The hair is then rinsed, washed and dried.
  • a product having dispersing and wetting properties such as sulphonated lauryl alcohol
  • the hairs are dyed a shade from golden blonde to light auburn.
  • a hair-dyeing composition comprising an intimate mixture of a compound free from any solubilizing group and represented by the formula (WP-X O H wherein X is a monovalent radical selected from the class consisting of hydrogen, halogens, alkyl, alkoxy and bydroxyalkyl groups, a me rcaptan reducing agent represented by the formula wherein R is a bivalent aliphatic residue and Y is selected from the class consisting of hydrogen and a carboxyl group, in combination with a base added immediately prior to the application of said composition to the hair, said base being selected from the class consisting of ammonia, an aliphatic amine and a cycloaliphatic amine.
  • WP-X O H wherein X is a monovalent radical selected from the class consisting of hydrogen, halogens, alkyl, alkoxy and bydroxyalkyl groups, a me rcaptan reducing agent represented by the formula wherein R is a bivalent aliphatic
  • a hair-dyeing composition comprising an intimate mixture of a compound free from any solubilizing group and represented by the formula wherein X is a monovalent radical selected from the class consisting of a hydrogen, halogens, alkyl, alkoxy and hydroxyalkyl groups, a mercaptan reducing agent represented by the formula wherein R is a bivalent aliphatic residue and Y is selected from the class consisting of hydrogen and a carboxyl group, in combination with a salt adapted to liberate a base added immediately prior to the application of said composition to the hair, said base being selected from the class consisting of ammonia, an aliphatic amine and a cycloaliphatic amine.

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  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Emergency Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Cosmetics (AREA)
US2733186D 1951-04-19 Compositions for the dyeing of hair Expired - Lifetime US2733186A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
MA301590X 1951-04-19
MA754948X 1953-03-26

Publications (1)

Publication Number Publication Date
US2733186A true US2733186A (en) 1956-01-31

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US2733186D Expired - Lifetime US2733186A (en) 1951-04-19 Compositions for the dyeing of hair

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US (1) US2733186A (es)
BE (2) BE527394A (es)
CH (2) CH301590A (es)
DE (1) DE1003402B (es)
FR (2) FR1036111A (es)
GB (2) GB710134A (es)
NL (1) NL75665C (es)

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2975101A (en) * 1957-01-22 1961-03-14 Oreal Dyeing of hair and other keratinous materials
US3920384A (en) * 1974-07-17 1975-11-18 Clairol Inc Autoxidizable hair dye containing preparations
US3954393A (en) * 1973-08-29 1976-05-04 Combe, Inc. Hair dyeing composition containing bismuth citrate, triethanolamine and sulfur
US4054413A (en) * 1974-07-17 1977-10-18 Clairol Incorporated Autoxidizable hair dye containing preparations
US4195972A (en) * 1978-10-20 1980-04-01 Combe Incorporated Aqueous-based hair dyeing composition containing a soluble bismuth salt and a reducing compound
US4306873A (en) * 1978-10-20 1981-12-22 Combe Incorporated Aqueous-based hair dyeing composition containing a soluble bismuth salt complex and a reducing compound

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
BE563221A (es) * 1956-12-19
GB1489344A (en) * 1974-01-18 1977-10-19 Unilever Ltd Hair dyeing composition
FR2338036A1 (fr) * 1976-01-19 1977-08-12 Oreal Compositions tinctoriales a base de diphenylamines et de polyhydroxybenzenes
FR2421606A1 (fr) * 1978-04-06 1979-11-02 Oreal Procede de teinture de fibres keratiniques en deux temps
FR2500748A1 (fr) * 1981-02-27 1982-09-03 Oreal Nouvelle composition de teinture des cheveux contenant en melange une poudre vegetale non epuisee, un colorant d'origine naturelle et un agent diluant

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB486086A (en) * 1934-10-03 1938-05-26 Franz Stroeher A G Dyeing medium for live hair
US2162458A (en) * 1936-05-08 1939-06-13 Winthrop Chem Co Inc Hair dye
FR951538A (fr) * 1946-12-14 1949-10-27 Oreal Maroc Perfectionnements aux teintures pour cheveux

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE663781C (de) * 1936-05-08 1938-08-13 I G Farbenindustrie Akt Ges Haarfaerbemittel
GB673489A (en) * 1949-05-09 1952-06-04 Dirk Jan Donker Improvements in or relating to colouring natural hair

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB486086A (en) * 1934-10-03 1938-05-26 Franz Stroeher A G Dyeing medium for live hair
US2162458A (en) * 1936-05-08 1939-06-13 Winthrop Chem Co Inc Hair dye
FR951538A (fr) * 1946-12-14 1949-10-27 Oreal Maroc Perfectionnements aux teintures pour cheveux
US2610941A (en) * 1946-12-14 1952-09-16 L Oreal Soc Hair-dye compositions

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2975101A (en) * 1957-01-22 1961-03-14 Oreal Dyeing of hair and other keratinous materials
US3954393A (en) * 1973-08-29 1976-05-04 Combe, Inc. Hair dyeing composition containing bismuth citrate, triethanolamine and sulfur
US3920384A (en) * 1974-07-17 1975-11-18 Clairol Inc Autoxidizable hair dye containing preparations
US4054413A (en) * 1974-07-17 1977-10-18 Clairol Incorporated Autoxidizable hair dye containing preparations
US4195972A (en) * 1978-10-20 1980-04-01 Combe Incorporated Aqueous-based hair dyeing composition containing a soluble bismuth salt and a reducing compound
US4306873A (en) * 1978-10-20 1981-12-22 Combe Incorporated Aqueous-based hair dyeing composition containing a soluble bismuth salt complex and a reducing compound

Also Published As

Publication number Publication date
GB754948A (en) 1956-08-15
CH301590A (fr) 1954-09-15
GB710134A (en) 1954-06-09
FR1036111A (fr) 1953-09-03
NL75665C (es)
CH318135A (fr) 1956-12-15
FR65507E (fr) 1956-02-28
BE506535A (es)
BE527394A (es)
DE1003402B (de) 1957-02-28

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