US3194735A - Hair coloring comprising a basic dye, a glycol and an amphoteric surfactant - Google Patents
Hair coloring comprising a basic dye, a glycol and an amphoteric surfactant Download PDFInfo
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- US3194735A US3194735A US342518A US34251864A US3194735A US 3194735 A US3194735 A US 3194735A US 342518 A US342518 A US 342518A US 34251864 A US34251864 A US 34251864A US 3194735 A US3194735 A US 3194735A
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- hair
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- dye
- glycol
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- 230000037308 hair color Effects 0.000 title description 12
- 239000000981 basic dye Substances 0.000 title description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 title description 8
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 title description 4
- 239000002280 amphoteric surfactant Substances 0.000 title description 2
- 239000000203 mixture Substances 0.000 claims description 43
- 239000004094 surface-active agent Substances 0.000 claims description 12
- 238000004040 coloring Methods 0.000 claims description 7
- 150000001875 compounds Chemical class 0.000 claims description 5
- 239000007864 aqueous solution Substances 0.000 claims description 2
- 239000000975 dye Substances 0.000 description 18
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 10
- 125000004432 carbon atom Chemical group C* 0.000 description 6
- XYYUAOIALFMRGY-UHFFFAOYSA-N 3-[2-carboxyethyl(dodecyl)amino]propanoic acid Chemical compound CCCCCCCCCCCCN(CCC(O)=O)CCC(O)=O XYYUAOIALFMRGY-UHFFFAOYSA-N 0.000 description 5
- 229940051250 hexylene glycol Drugs 0.000 description 5
- 239000000443 aerosol Substances 0.000 description 4
- 159000000000 sodium salts Chemical class 0.000 description 4
- UCMIRNVEIXFBKS-UHFFFAOYSA-N beta-alanine Chemical compound NCCC(O)=O UCMIRNVEIXFBKS-UHFFFAOYSA-N 0.000 description 3
- 230000003806 hair structure Effects 0.000 description 3
- 229910052751 metal Inorganic materials 0.000 description 3
- 239000002184 metal Substances 0.000 description 3
- 238000000034 method Methods 0.000 description 3
- 230000009972 noncorrosive effect Effects 0.000 description 3
- GSQFUEPQVUSAPE-UHFFFAOYSA-N 2-methylpentane-2,3-diol Chemical compound CCC(O)C(C)(C)O GSQFUEPQVUSAPE-UHFFFAOYSA-N 0.000 description 2
- HIYKOZFIVZIBFO-UHFFFAOYSA-N 3-methylpentane-1,3-diol Chemical compound CCC(C)(O)CCO HIYKOZFIVZIBFO-UHFFFAOYSA-N 0.000 description 2
- 229910052783 alkali metal Inorganic materials 0.000 description 2
- 150000001340 alkali metals Chemical class 0.000 description 2
- 238000004061 bleaching Methods 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 238000001704 evaporation Methods 0.000 description 2
- 230000008020 evaporation Effects 0.000 description 2
- QCIYAEYRVFUFAP-UHFFFAOYSA-N hexane-2,3-diol Chemical compound CCCC(O)C(C)O QCIYAEYRVFUFAP-UHFFFAOYSA-N 0.000 description 2
- OHMBHFSEKCCCBW-UHFFFAOYSA-N hexane-2,5-diol Chemical compound CC(O)CCC(C)O OHMBHFSEKCCCBW-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 150000003839 salts Chemical class 0.000 description 2
- -1 Color Index #46005 Chemical compound 0.000 description 1
- GSEJCLTVZPLZKY-UHFFFAOYSA-N Triethanolamine Chemical class OCCN(CCO)CCO GSEJCLTVZPLZKY-UHFFFAOYSA-N 0.000 description 1
- 230000002378 acidificating effect Effects 0.000 description 1
- DPKHZNPWBDQZCN-UHFFFAOYSA-N acridine orange free base Chemical compound C1=CC(N(C)C)=CC2=NC3=CC(N(C)C)=CC=C3C=C21 DPKHZNPWBDQZCN-UHFFFAOYSA-N 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 125000002947 alkylene group Chemical group 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- DZBUGLKDJFMEHC-UHFFFAOYSA-N benzoquinolinylidene Natural products C1=CC=CC2=CC3=CC=CC=C3N=C21 DZBUGLKDJFMEHC-UHFFFAOYSA-N 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 235000019864 coconut oil Nutrition 0.000 description 1
- 239000003240 coconut oil Substances 0.000 description 1
- PXBRQCKWGAHEHS-UHFFFAOYSA-N dichlorodifluoromethane Chemical compound FC(F)(Cl)Cl PXBRQCKWGAHEHS-UHFFFAOYSA-N 0.000 description 1
- 235000019404 dichlorodifluoromethane Nutrition 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 239000012153 distilled water Substances 0.000 description 1
- 230000007613 environmental effect Effects 0.000 description 1
- 230000001747 exhibiting effect Effects 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 239000006260 foam Substances 0.000 description 1
- 238000005187 foaming Methods 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 239000000118 hair dye Substances 0.000 description 1
- TXGJTWACJNYNOJ-UHFFFAOYSA-N hexane-2,4-diol Chemical compound CCC(O)CC(C)O TXGJTWACJNYNOJ-UHFFFAOYSA-N 0.000 description 1
- SYGRIMFNUFCHJC-UHFFFAOYSA-N hydron;4-methyl-6-phenyldiazenylbenzene-1,3-diamine;chloride Chemical compound Cl.C1=C(N)C(C)=CC(N=NC=2C=CC=CC=2)=C1N SYGRIMFNUFCHJC-UHFFFAOYSA-N 0.000 description 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 1
- CXKWCBBOMKCUKX-UHFFFAOYSA-M methylene blue Chemical compound [Cl-].C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 CXKWCBBOMKCUKX-UHFFFAOYSA-M 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 239000007800 oxidant agent Substances 0.000 description 1
- 239000002304 perfume Substances 0.000 description 1
- 230000001376 precipitating effect Effects 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 239000003380 propellant Substances 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 210000004761 scalp Anatomy 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000010186 staining Methods 0.000 description 1
- 125000001424 substituent group Chemical group 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 239000003760 tallow Substances 0.000 description 1
- 230000001052 transient effect Effects 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
- A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives 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
- A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
- A61K8/34—Alcohols
- A61K8/345—Alcohols containing more than one hydroxy group
-
- 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
Definitions
- This invention relates to a composition of matter and more particularly, to new and novel compositions especially useful for coloring human hair, and to methods for their use.
- compositions for coloring the human hair have been known and widely used for many years.
- the first compositions which were developed for this purpose were those which utilized dyes which acted to dye the hair in the presence of certain auxiliary agents, such as oxidizing agents, dye precipitating agents and the like.
- auxiliary agents such as oxidizing agents, dye precipitating agents and the like.
- the dye becomes permanently absorbed'in the hair structure and should the user become dissatisfied with the particular color employed little can be done except to subject the hair to a very strenuous bleaching treatment and then re-dye the-hair.
- the other alternative is to permit the hair to grow out, cutting the dyed portions from time to time until only the natural hair remains.
- strenuous bleaching compositions irritating to the skin but they tend to alter and embrittle the hair structure.
- compositions comprising water soluble basic dyes in combination with nonionic surface active agents imparted a desirable color to the hair which could, if desired, be removed by merely shampooing several times which served to solve many of the problems associated with the old permanent type'compositions.
- compositions of this type of transient hair coloring are disclosed in US. Patent No. 2,763,269.
- 'It is a further object of this invention to provide a hair coloring composition which when applied to hair has sufficient permanency to withstand change under the normal environmental conditions yet may be easily removed by shampooing.
- hair coloring compositions which are formulated by combining water soluble basic dyes with a particular class of amphoteric surface active agents and adding from about 2 to about 15 percent by weight of a hexylene glycol to the composition.
- hexylene glycol refers to saturated compounds having 6 carbon atoms in a straight or branched chain structure and further substituted with 2 hydroxyl groups.
- Such compounds have the empirical formula C H (OH) Exemplary of such compounds are 2-methyl-2,4-pentanediol, 2,3-hexanediol, 2,4-hexanediol, 2,5-hexanediol, 2- ethyl-2,4-butanediol, 2-methyl-2,3-pentanediol and the like.
- the dyes employed in said improved hair coloring composition are of the Water soluble basic type, the exact dye or combination of dyes employed being governed by the desired shade to be imparted to the hair by the composition.
- Typical water soluble basic dyes which are useful in formulating hair'coloring compositions according to this invention are Acridine Orange, Color Index #46005, Methylene Blue, Calcozine Orange RS, Color coloring composition by employing the combination of an amphoteric surface active agent with a hexylene glycol, the concentration of water soluble basic dyes necessary in compositions of this invention is at least 25 percent less than is necessary in similar compositions for a comparable take on the hair utilizing said water soluble basic dyes but which do not include this combination of amphoteric surface active agent with hexylene glycol.
- the surface active agent used in the compositions are amphoteric and contain both acidic and basic functional groups. I have found that the straight chain amphoteric surface active agents of the formula:
- R is an alkyl radical containing 8 to 20 carbon atoms
- A is an alkylene radical, of either straight or branched chain structure, containing 1 to 8 carbon atoms
- the alkali metal and triethanolamine salts thereof are particularly advantageous because they do not leave a film on the hair after rinsing and evaporation.
- the dye therefore, not being entrapped in a film has a better chance to combine with the hair structure and, in fact, the dye is actually absorbed on' the hair.
- the R, substituent may derive either from purified carboxylic acids having the desired number of carbon atoms or, alternately, may be the mixed alkyl radicals derived from the fatty acids of such natural materials as coconut oil, tallow and the like.
- straight chain amphoteric surface active agents are those identified by the trademark Deriphat of General Mills, Inc., Kankakee, 111., including Deriphat 151 which is the sodium salt of N-coco beta amino propionate, Deriphat 170 which is the sodium salt of N-lauryl beta amino propionate and Deriphat 1703 which is the triethanolarnine salt of N-lauryl beta amino propionate.
- compositions of this invention preferably contain about 2 to about 15 percent by weight of amphoteric surface active agent and have a pH between about 6 and about 7.
- heXylene glycol in the composition i an amount of about 2 to about percent by weight serves 1 to aid solubilizati-on of the basic dye in the system.
- compositions of this invention are stable, possess an optimum degree of dye utilization on the hair and are substantially noncor-rosive, a property of particular advantage when the composition is pack-aged under pressure in a metal can for aerosol application.
- a package will also contain suitable liquified gaseous propellants, that is, one or more of the chlorofluorocarbons conventionally used for such purposes.
- the compositions of this invention may also include conventional perfumes, preservatives and hair-conditioning agents. In use, the consumer selects the desired shade and then shampoos her hair with the composition. When the hair has been Washed and dried, the hair assumes the color of the selected shade. The color will resist normal handling, i.e., it will not rub off or will not discolor in the presence of moisture.
- Example 1 A hair coloring composition adapted to impart a blond color to the hair is formulated at a pH of 6.5 to contain:
- Example 2 The composition of Example 1 is prepared, with the substitution of 4.5 parts of dichl-orodifiu-oromethane (Freon 12) and 3.0 parts of l,2-dichloro-1,1,2,2-tetrafiu-oroethane for 7.5 parts of distilled Water.
- composition for coloring human hair which comprises an aqueous solution containing between about 2 and about 15 percent by weight of a surface active agent selected from the group consisting of compounds of the formula:
- R is alkyl of 8 to 20 carbon atoms and A is alkylene of 1 to 8 carbon atoms and the alkali metal and triethanolarnine salts thereof, between about 0.04 and about 1.5 percent by weight of .a water soluble basic hair dye, and from about 2 to about 15 percent by Weight of glycol having the formula C H (OH) 4 2.
- said surface active agent is the sodium salt of N-coco beta amino propionate.
- a composition according to claim 1 wherein said glycol is a member of the group consisting of 2-methyl-2,4- pentanediol, 2,3-hexanediol, 2,4-hexanedi0l, 2,5-hexanediol, 2-ethyl-2,4-butanediol, and 2- methyl-2,3-pentanediol.
- a method for coloringhair which comprises shampooing the hair, with a composition as defined in claim 1, rinsing the shampooed hair with water until the water runs clear and allowing the hair to dry.
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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)
- Birds (AREA)
- Epidemiology (AREA)
- Emergency Medicine (AREA)
- Cosmetics (AREA)
Description
United States Patent Office 3,104,735 Patented July 13, 1965 3,194,735 HAIR COLORING COMPRISING A BASIC DYE,
A GLYCOL AND AN AMPHOTERIC SUR- FACTANT Stanley Brechner, West Orange, N.J., assignor to Warner- Lambert Pharmaceutical Company, Morris Plains, N.J.,
a corporation of Delaware No Drawing. Filed Feb. 4, 1964, Ser. No. 342,518 4 Claims. (Cl. 167-88) This invention relates to a composition of matter and more particularly, to new and novel compositions especially useful for coloring human hair, and to methods for their use.
This application is a continuation-in-part of copending application Serial No. 65,580 filed October 28, 1960, now abandoned.
Compositions for coloring the human hair have been known and widely used for many years. The first compositions which were developed for this purpose were those which utilized dyes which acted to dye the hair in the presence of certain auxiliary agents, such as oxidizing agents, dye precipitating agents and the like. When such compositions are applied to the hair, the dye becomes permanently absorbed'in the hair structure and should the user become dissatisfied with the particular color employed little can be done except to subject the hair to a very strenuous bleaching treatment and then re-dye the-hair. The other alternative is to permit the hair to grow out, cutting the dyed portions from time to time until only the natural hair remains. Not only are strenuous bleaching compositions irritating to the skin but they tend to alter and embrittle the hair structure.
It was later found that compositions comprising water soluble basic dyes in combination with nonionic surface active agents imparted a desirable color to the hair which could, if desired, be removed by merely shampooing several times which served to solve many of the problems associated with the old permanent type'compositions. Compositions of this type of transient hair coloring are disclosed in US. Patent No. 2,763,269.
' These improved compositions, however, have certain disadvantages. It has been found that the human hair does not tend to absord or take these basic dyes to a satisfactory degree in the presence of significant quantities of nonionic surface active agents. Thus, to produce a color take on the hair to the desired depth the dye concentration in the product must be raised to a point at which the compositions frequently cause objectionable and unsightly staining of the hands and scalp of the person applying the composition. Aerosol spray application has been well accepted by consumers in recent years and compositions for coloring the hair have been packaged in this form. There has, furthermore, long been a need for an aqueous hair coloring composition with a high degree of dye utilization which may be conveniently packaged in the form of an aerosol. Since the latter are normally packaged in metal cans, it is of importance that these compositions be noncorrosive in order to insure long shelf life when packaged in such containers.
Recently issued US. Patent No. 3,092,555 describes a foaming composition for carrying hair coloring materials. While such a composition does represent an improvement, it is still far from satisfactory for use in hair coloring procedures. Thus, for example, when a dye is incorporated into such a composition and applied to human hair, upon evaporation of the foam a uniform film containing entrapped dyes is deposited on the hair. It is quite obvious that a mere deposit of the dye trapped in a film deposited on the hair can be easily rubbed off on linens or clothing or, if the colored hair is wetted, the dye will dissolve and will streak the face, the clothes and so on.
It is, therefore, an important object of this invention to provide a hair coloring composition exhibiting a high and efficient degree of dye take or utilization.
'It is a further object of this invention to provide a hair coloring composition which when applied to hair has sufficient permanency to withstand change under the normal environmental conditions yet may be easily removed by shampooing.
It is a further object of this invention to provide a hair coloring composition suitable for application in aerosol form and noncorrosive when packaged in metal cans.
Other objects and advantages of the present invention will become apparent from the following detailed description.
I have found quite unexpectedly that the aforesaid objects and advantages are attained with hair coloring compositions which are formulated by combining water soluble basic dyes with a particular class of amphoteric surface active agents and adding from about 2 to about 15 percent by weight of a hexylene glycol to the composition.
The term hexylene glycol as used in the specification and in the claims refers to saturated compounds having 6 carbon atoms in a straight or branched chain structure and further substituted with 2 hydroxyl groups. Such compounds have the empirical formula C H (OH) Exemplary of such compounds are 2-methyl-2,4-pentanediol, 2,3-hexanediol, 2,4-hexanediol, 2,5-hexanediol, 2- ethyl-2,4-butanediol, 2-methyl-2,3-pentanediol and the like.
The dyes employed in said improved hair coloring composition are of the Water soluble basic type, the exact dye or combination of dyes employed being governed by the desired shade to be imparted to the hair by the composition. Typical water soluble basic dyes which are useful in formulating hair'coloring compositions according to this invention are Acridine Orange, Color Index #46005, Methylene Blue, Calcozine Orange RS, Color coloring composition by employing the combination of an amphoteric surface active agent with a hexylene glycol, the concentration of water soluble basic dyes necessary in compositions of this invention is at least 25 percent less than is necessary in similar compositions for a comparable take on the hair utilizing said water soluble basic dyes but which do not include this combination of amphoteric surface active agent with hexylene glycol.
The surface active agent used in the compositions are amphoteric and contain both acidic and basic functional groups. I have found that the straight chain amphoteric surface active agents of the formula:
wherein R is an alkyl radical containing 8 to 20 carbon atoms, and A is an alkylene radical, of either straight or branched chain structure, containing 1 to 8 carbon atoms, and the alkali metal and triethanolamine salts thereof are particularly advantageous because they do not leave a film on the hair after rinsing and evaporation. The dye, therefore, not being entrapped in a film has a better chance to combine with the hair structure and, in fact, the dye is actually absorbed on' the hair.
The R, substituent may derive either from purified carboxylic acids having the desired number of carbon atoms or, alternately, may be the mixed alkyl radicals derived from the fatty acids of such natural materials as coconut oil, tallow and the like. Exemplary of such straight chain amphoteric surface active agents are those identified by the trademark Deriphat of General Mills, Inc., Kankakee, 111., including Deriphat 151 which is the sodium salt of N-coco beta amino propionate, Deriphat 170 which is the sodium salt of N-lauryl beta amino propionate and Deriphat 1703 which is the triethanolarnine salt of N-lauryl beta amino propionate.
The compositions of this invention preferably contain about 2 to about 15 percent by weight of amphoteric surface active agent and have a pH between about 6 and about 7.
The presence of heXylene glycol in the composition i an amount of about 2 to about percent by weight serves 1 to aid solubilizati-on of the basic dye in the system.
The resulting compositions are stable, possess an optimum degree of dye utilization on the hair and are substantially noncor-rosive, a property of particular advantage when the composition is pack-aged under pressure in a metal can for aerosol application. Such a package will also contain suitable liquified gaseous propellants, that is, one or more of the chlorofluorocarbons conventionally used for such purposes. The compositions of this invention may also include conventional perfumes, preservatives and hair-conditioning agents. In use, the consumer selects the desired shade and then shampoos her hair with the composition. When the hair has been Washed and dried, the hair assumes the color of the selected shade. The color will resist normal handling, i.e., it will not rub off or will not discolor in the presence of moisture.
The following examples are included in order further to illustrate the present invention:
Example 1 A hair coloring composition adapted to impart a blond color to the hair is formulated at a pH of 6.5 to contain:
Parts by weight Deriphat 151* 3 0 General Mills, Inc., Kanknkee, Ill. The sodium salt of N-coco beta amino propionate.
Example 2 The composition of Example 1 is prepared, with the substitution of 4.5 parts of dichl-orodifiu-oromethane (Freon 12) and 3.0 parts of l,2-dichloro-1,1,2,2-tetrafiu-oroethane for 7.5 parts of distilled Water.
It is understood that the foregoing detailed description is given merely by way of illustration and that many variations may be made there-in without departing from the spirit of my invention.
Having described my invention, What I desire to secure by Letters Patent is:
1. A composition for coloring human hair which comprises an aqueous solution containing between about 2 and about 15 percent by weight of a surface active agent selected from the group consisting of compounds of the formula:
wherein R is alkyl of 8 to 20 carbon atoms and A is alkylene of 1 to 8 carbon atoms and the alkali metal and triethanolarnine salts thereof, between about 0.04 and about 1.5 percent by weight of .a water soluble basic hair dye, and from about 2 to about 15 percent by Weight of glycol having the formula C H (OH) 4 2. A composition according to claim 1 wherein said surface active agent is the sodium salt of N-coco beta amino propionate.
3. A composition according to claim 1 wherein said glycol is a member of the group consisting of 2-methyl-2,4- pentanediol, 2,3-hexanediol, 2,4-hexanedi0l, 2,5-hexanediol, 2-ethyl-2,4-butanediol, and 2- methyl-2,3-pentanediol.
4-. A method for coloringhair which comprises shampooing the hair, with a composition as defined in claim 1, rinsing the shampooed hair with water until the water runs clear and allowing the hair to dry.
References Cited by the Examiner UNITED STATESPATENTS 8/56 Den Beste 16788 6/63 Horn 16788 OTHER REFERENCES JULIAN S. LEVITT, Primary Examiner.
Claims (1)
1. A COMPOSITION FOR COLORING HUMAN HAIR WHICH COMPRISES AN AQUEOUS SOLUTION CONTAINING BETWEEN ABOUT 2 AND ABOUT 15 PERCENT BY WEIGHT OF A SURFACE ACTIVE AGENT SELECTED FROM THE GROUP CONSISTING OF COMPOUNDS OF FORMULA
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US342518A US3194735A (en) | 1964-02-04 | 1964-02-04 | Hair coloring comprising a basic dye, a glycol and an amphoteric surfactant |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US342518A US3194735A (en) | 1964-02-04 | 1964-02-04 | Hair coloring comprising a basic dye, a glycol and an amphoteric surfactant |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US3194735A true US3194735A (en) | 1965-07-13 |
Family
ID=23342179
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US342518A Expired - Lifetime US3194735A (en) | 1964-02-04 | 1964-02-04 | Hair coloring comprising a basic dye, a glycol and an amphoteric surfactant |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US3194735A (en) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3331781A (en) * | 1962-02-15 | 1967-07-18 | Oreal | Amphoteric surface-active agents and method of preparing them |
| US3480377A (en) * | 1964-05-06 | 1969-11-25 | Lever Brothers Ltd | Solvent dyeing of living human hair |
| US3920807A (en) * | 1970-08-18 | 1975-11-18 | Lever Brothers Ltd | Antiperspirant and deodorant compositions |
| US4087240A (en) * | 1974-01-22 | 1978-05-02 | Ciba-Geigy Corporation | Stable formulations of textile-processing agents |
| US4168144A (en) * | 1970-11-06 | 1979-09-18 | Lever Brothers Company | Keratinous fibers colorant compositions containing basic dyes and an anionic-cationic detergent complex |
| US5948124A (en) * | 1996-07-15 | 1999-09-07 | Kao Corporation | Composition for dyeing human hair comprising a cationic dye, a zwitterionic surfactant, and an anionic UV-absorber |
Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2763269A (en) * | 1952-02-01 | 1956-09-18 | Rayette Inc | Foaming hair coloring compositions comprising basic dyes, and method of use |
| US3092555A (en) * | 1958-04-21 | 1963-06-04 | Roy H Horn | Relatively collapsible aerosol foam compositions |
-
1964
- 1964-02-04 US US342518A patent/US3194735A/en not_active Expired - Lifetime
Patent Citations (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2763269A (en) * | 1952-02-01 | 1956-09-18 | Rayette Inc | Foaming hair coloring compositions comprising basic dyes, and method of use |
| US3092555A (en) * | 1958-04-21 | 1963-06-04 | Roy H Horn | Relatively collapsible aerosol foam compositions |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US3331781A (en) * | 1962-02-15 | 1967-07-18 | Oreal | Amphoteric surface-active agents and method of preparing them |
| US3480377A (en) * | 1964-05-06 | 1969-11-25 | Lever Brothers Ltd | Solvent dyeing of living human hair |
| US3920807A (en) * | 1970-08-18 | 1975-11-18 | Lever Brothers Ltd | Antiperspirant and deodorant compositions |
| US4168144A (en) * | 1970-11-06 | 1979-09-18 | Lever Brothers Company | Keratinous fibers colorant compositions containing basic dyes and an anionic-cationic detergent complex |
| US4087240A (en) * | 1974-01-22 | 1978-05-02 | Ciba-Geigy Corporation | Stable formulations of textile-processing agents |
| US5948124A (en) * | 1996-07-15 | 1999-09-07 | Kao Corporation | Composition for dyeing human hair comprising a cationic dye, a zwitterionic surfactant, and an anionic UV-absorber |
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