US3369970A - Dyeing human hair - Google Patents
Dyeing human hair Download PDFInfo
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- US3369970A US3369970A US593581A US59358166A US3369970A US 3369970 A US3369970 A US 3369970A US 593581 A US593581 A US 593581A US 59358166 A US59358166 A US 59358166A US 3369970 A US3369970 A US 3369970A
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- hair
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- dye
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- dyes
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- 210000004209 hair Anatomy 0.000 title description 28
- 238000004043 dyeing Methods 0.000 title description 11
- 239000000203 mixture Substances 0.000 description 44
- 239000000981 basic dye Substances 0.000 description 22
- 239000000975 dye Substances 0.000 description 22
- 239000003921 oil Substances 0.000 description 14
- 239000004519 grease Substances 0.000 description 12
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- 239000004094 surface-active agent Substances 0.000 description 11
- 239000000118 hair dye Substances 0.000 description 10
- 239000000126 substance Substances 0.000 description 8
- 238000012505 colouration Methods 0.000 description 6
- 239000012736 aqueous medium Substances 0.000 description 5
- 239000000986 disperse dye Substances 0.000 description 5
- 239000004615 ingredient Substances 0.000 description 5
- 239000002609 medium Substances 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 4
- CDBYLPFSWZWCQE-UHFFFAOYSA-L Sodium Carbonate Chemical compound [Na+].[Na+].[O-]C([O-])=O CDBYLPFSWZWCQE-UHFFFAOYSA-L 0.000 description 4
- 125000002091 cationic group Chemical group 0.000 description 4
- UQGFMSUEHSUPRD-UHFFFAOYSA-N disodium;3,7-dioxido-2,4,6,8,9-pentaoxa-1,3,5,7-tetraborabicyclo[3.3.1]nonane Chemical compound [Na+].[Na+].O1B([O-])OB2OB([O-])OB1O2 UQGFMSUEHSUPRD-UHFFFAOYSA-N 0.000 description 4
- 229930195733 hydrocarbon Natural products 0.000 description 4
- 150000002430 hydrocarbons Chemical class 0.000 description 4
- 239000007788 liquid Substances 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- 238000003860 storage Methods 0.000 description 4
- 239000002562 thickening agent Substances 0.000 description 4
- 238000005406 washing Methods 0.000 description 4
- 240000005020 Acaciella glauca Species 0.000 description 3
- LZZYPRNAOMGNLH-UHFFFAOYSA-M Cetrimonium bromide Chemical compound [Br-].CCCCCCCCCCCCCCCC[N+](C)(C)C LZZYPRNAOMGNLH-UHFFFAOYSA-M 0.000 description 3
- 239000005662 Paraffin oil Substances 0.000 description 3
- 239000000945 filler Substances 0.000 description 3
- 229920000609 methyl cellulose Polymers 0.000 description 3
- 239000001923 methylcellulose Substances 0.000 description 3
- 235000010981 methylcellulose Nutrition 0.000 description 3
- 230000003647 oxidation Effects 0.000 description 3
- 238000007254 oxidation reaction Methods 0.000 description 3
- 239000002304 perfume Substances 0.000 description 3
- 235000003499 redwood Nutrition 0.000 description 3
- VTYYLEPIZMXCLO-UHFFFAOYSA-L Calcium carbonate Chemical compound [Ca+2].[O-]C([O-])=O VTYYLEPIZMXCLO-UHFFFAOYSA-L 0.000 description 2
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 2
- PMZURENOXWZQFD-UHFFFAOYSA-L Sodium Sulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=O PMZURENOXWZQFD-UHFFFAOYSA-L 0.000 description 2
- 229910000288 alkali metal carbonate Inorganic materials 0.000 description 2
- 150000008041 alkali metal carbonates Chemical class 0.000 description 2
- 150000001768 cations Chemical class 0.000 description 2
- 239000007859 condensation product Substances 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- JVICFMRAVNKDOE-UHFFFAOYSA-M ethyl violet Chemical compound [Cl-].C1=CC(N(CC)CC)=CC=C1C(C=1C=CC(=CC=1)N(CC)CC)=C1C=CC(=[N+](CC)CC)C=C1 JVICFMRAVNKDOE-UHFFFAOYSA-M 0.000 description 2
- RKJUIXBNRJVNHR-UHFFFAOYSA-N indolenine group Chemical group N1=CCC2=CC=CC=C12 RKJUIXBNRJVNHR-UHFFFAOYSA-N 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- -1 oxonium cation Chemical class 0.000 description 2
- 229910000029 sodium carbonate Inorganic materials 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- PNXWPUCNFMVBBK-UHFFFAOYSA-M 1-dodecylpyridin-1-ium;bromide Chemical compound [Br-].CCCCCCCCCCCC[N+]1=CC=CC=C1 PNXWPUCNFMVBBK-UHFFFAOYSA-M 0.000 description 1
- YFVBASFBIJFBAI-UHFFFAOYSA-M 1-tetradecylpyridin-1-ium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+]1=CC=CC=C1 YFVBASFBIJFBAI-UHFFFAOYSA-M 0.000 description 1
- RBTBFTRPCNLSDE-UHFFFAOYSA-N 3,7-bis(dimethylamino)phenothiazin-5-ium Chemical compound C1=CC(N(C)C)=CC2=[S+]C3=CC(N(C)C)=CC=C3N=C21 RBTBFTRPCNLSDE-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 229920000742 Cotton Polymers 0.000 description 1
- 241000997826 Melanocetus johnsonii Species 0.000 description 1
- AOMUHOFOVNGZAN-UHFFFAOYSA-N N,N-bis(2-hydroxyethyl)dodecanamide Chemical compound CCCCCCCCCCCC(=O)N(CCO)CCO AOMUHOFOVNGZAN-UHFFFAOYSA-N 0.000 description 1
- IGFHQQFPSIBGKE-UHFFFAOYSA-N Nonylphenol Natural products CCCCCCCCCC1=CC=C(O)C=C1 IGFHQQFPSIBGKE-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 125000000217 alkyl group Chemical group 0.000 description 1
- 239000013566 allergen Substances 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 239000010975 amethyst Substances 0.000 description 1
- 239000010775 animal oil Substances 0.000 description 1
- 125000000129 anionic group Chemical group 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- 230000003078 antioxidant effect Effects 0.000 description 1
- 235000006708 antioxidants Nutrition 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- 229910021538 borax Inorganic materials 0.000 description 1
- 229910000019 calcium carbonate Inorganic materials 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 239000013078 crystal Substances 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 230000005484 gravity Effects 0.000 description 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-M hydroxide Chemical compound [OH-] XLYOFNOQVPJJNP-UHFFFAOYSA-M 0.000 description 1
- 229940031957 lauric acid diethanolamide Drugs 0.000 description 1
- 230000001050 lubricating effect Effects 0.000 description 1
- 229940107698 malachite green Drugs 0.000 description 1
- FDZZZRQASAIRJF-UHFFFAOYSA-M malachite green Chemical compound [Cl-].C1=CC(N(C)C)=CC=C1C(C=1C=CC=CC=1)=C1C=CC(=[N+](C)C)C=C1 FDZZZRQASAIRJF-UHFFFAOYSA-M 0.000 description 1
- 229910052751 metal Inorganic materials 0.000 description 1
- 239000002184 metal Substances 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 229960000907 methylthioninium chloride Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- 230000009972 noncorrosive effect Effects 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- SNQQPOLDUKLAAF-UHFFFAOYSA-N nonylphenol Chemical compound CCCCCCCCCC1=CC=CC=C1O SNQQPOLDUKLAAF-UHFFFAOYSA-N 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 229910052760 oxygen Inorganic materials 0.000 description 1
- AFAIELJLZYUNPW-UHFFFAOYSA-N pararosaniline free base Chemical compound C1=CC(N)=CC=C1C(C=1C=CC(N)=CC=1)=C1C=CC(=N)C=C1 AFAIELJLZYUNPW-UHFFFAOYSA-N 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- 235000019271 petrolatum Nutrition 0.000 description 1
- 239000008194 pharmaceutical composition Substances 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- PYWVYCXTNDRMGF-UHFFFAOYSA-N rhodamine B Chemical compound [Cl-].C=12C=CC(=[N+](CC)CC)C=C2OC2=CC(N(CC)CC)=CC=C2C=1C1=CC=CC=C1C(O)=O PYWVYCXTNDRMGF-UHFFFAOYSA-N 0.000 description 1
- 229940043267 rhodamine b Drugs 0.000 description 1
- 239000012056 semi-solid material Substances 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate Nutrition 0.000 description 1
- 239000004328 sodium tetraborate Substances 0.000 description 1
- 235000010339 sodium tetraborate Nutrition 0.000 description 1
- 239000003381 stabilizer Substances 0.000 description 1
- SFVFIFLLYFPGHH-UHFFFAOYSA-M stearalkonium chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[N+](C)(C)CC1=CC=CC=C1 SFVFIFLLYFPGHH-UHFFFAOYSA-M 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-O sulfonium Chemical compound [SH3+] RWSOTUBLDIXVET-UHFFFAOYSA-O 0.000 description 1
- 239000000454 talc Substances 0.000 description 1
- 229910052623 talc Inorganic materials 0.000 description 1
- CEYYIKYYFSTQRU-UHFFFAOYSA-M trimethyl(tetradecyl)azanium;chloride Chemical compound [Cl-].CCCCCCCCCCCCCC[N+](C)(C)C CEYYIKYYFSTQRU-UHFFFAOYSA-M 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 210000002268 wool Anatomy 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
- A61K8/31—Hydrocarbons
-
- 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
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/20—Chemical, physico-chemical or functional or structural properties of the composition as a whole
- A61K2800/30—Characterized by the absence of a particular group of ingredients
- A61K2800/31—Anhydrous
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K2800/00—Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
- A61K2800/40—Chemical, physico-chemical or functional or structural properties of particular ingredients
- A61K2800/42—Colour properties
- A61K2800/43—Pigments; Dyes
- A61K2800/432—Direct dyes
Definitions
- This invention relates to the dyeing of human hair.
- Hair dyeing with synthethic dyes is usually performed by applying either disperse dyes or the so-called oxida-.
- tion dyes which are oxidised to a dye proper while in contact with the hair
- oxidation dyes have the disadvantage that they are allergens, and have to be used with great care; and disperse dyes generally produce a hair colouration that tends to be rather easily removable by washing.
- Basic dyes are a well-known class of dyes which are used in dyeing wool and cotton and in which that part of the dye molecule which confers colour and fibre aflinity (substantivity) on the whole is a cation, in particular an ammonium, sulphonium or oxonium cation.
- Such dyes have marked afi'inity for human hair when applied to it from an aqueous medium, and can be used safely to produce a hair colouration which is generally of greater permanence on washing than that imparted by disperse dyes.
- many basic dyes produce a hair colouration of intensity approaching that given by oxidation dyes.
- Basic dyes have a marked tendency to change in the presence of water to non-substantive materials, through destruction of the cationic charge as a result of the fusion of a hydroxyl ion, OH, with the dye cation; and the rate of this change, although usually low in comparison with that of preparative reactions, is yet high enough to be serious in compositions which are required to be storable for an extended period.
- the change is accelerated if the hair dye composition is formulated with a mildly alkaline-reacting water-soluble substance, such as borax or sodium carbonate, to improve uniformity of distribution of the dye along the length of the hair filaments during the actual dyeing procedure.
- a mildly alkaline-reacting water-soluble substance such as borax or sodium carbonate
- hair dye compositions of a form convenient for use and of good storage life can be obtained from a basic dye by mixing the powdered y with substantially water-immiscible oil or grease into the form of a viscous liquid or paste.
- Bo grease is mean a semi-solid material which readily flows under applied pressure, as lubricating grease does.
- the basic dye remains in solid form in the oil or grease medium, since such dyes are substantially insoluble in water-immiscible materials.
- transfer of the dye to the hair is not appreciable hindered by the water-immiscible oil or grease.
- the invention thus provides a hair dye composition in the form of a substantially anhydrous viscous liquid or paste comprising a powdered basic dye mixed with a water-immiscible oil or grease.
- the oil (which is suitably of Redwood viscosity greater than about seconds at 70 F.) or grease medium employed should of course be one that is non-toxic.
- a hydrocarbon as the water-immiscible medium is much to be preferred, although vegetable or animal oils or greases (whose molecules contain oxygen) can be used if an anti-oxidant or other stabiliser is also incorporated to inhibit the development of rancidity in them.
- Ordinary petroleum jelly is a suitable hydrocarbon grease; and suitable oils are parafiinic hydrocarbon oils such as refined light paraffin oil and medicinal parafiin.
- Basic dyes like disperse dyes and oxidation dyes, are applied to the hair from an aqueous medium in the presence of a surface-active agent, whose function is to reduce the natural water-repellency of hair and so facilitate intimate contact of the aqueous medium with the hair.
- a surface-active agent whose function is to reduce the natural water-repellency of hair and so facilitate intimate contact of the aqueous medium with the hair.
- a surfaceactive agent whose function is to reduce the natural water-repellency of hair and so facilitate intimate contact of the aqueous medium with the hair.
- a cationic or non-ionic surface-active agent may be used.
- Anionic surface-active agents are not compatible with the basic dye.
- Suitable cationic surface-active agents are long chain alkyl quaternary ammonium salts, such as cetyltrimethylammonium bromide, tetradecyltrimethylammonium chloride, laurylpyridinium bromide, tetradecylpyridinium chloride and stearyldimethylbenzylammonium chloride; and suitable non-ionic surface-active agents are long chain alkanolamides, such as lauric acid diethanolamide, and the condensation products of ethylene oxide or propylene oxide with a compound containing a long chain alkyl group and an active hydrogen atom, for example, the condensation product of nonylphenol with from 10 to 15 molar proportions of ethylene oxide.
- Incorporating a surface-active agent in a composition containing an oil (liquid) as distinct from a grease (semi-solid) has the further advantage of reducing the tendency of the dye particles to partly separate out from the oil ingredient on prolonged storage.
- the proportion of surface-active agent employed depends on whether the composition is intended to be applied direct to wetted hair or to be diluted with water immediately before application; a higher proportion will be required in the latter instance, in order to disperse the oil or grease medium in the larger volume of Water.
- the surface-active agent suitably forms from 2 to 25% by Weight of the composition.
- a thickener compatible with the dye is preferably incorporated in the composition, so that when the composition is brought into contact with water the aqueous mixture formed is sufficiently viscous to be worked about on the head without draining unduly quickly from it.
- Methyl cellulose is very satisfactory for the purpose.
- the proportion of thickener employed will be less when the composition is one intended for application direct to wetted hair than when the composition is to be diluted with water before being applied to the hair.
- the thickener suitably forms from 1 to 25% by weight of the composition.
- a mildly alkaline-reacting water-soluble substance can be incorporated in the composition, to improve distribution of the dye between the tips and roots of the hair during the dyeing procedure.
- Such substances are insoluble in the waterimmiscib1e oil or grease.
- the alkaline-reacting substance should be substantially water-free, for even 1% of weight of water in the composition will normally serious- 13 afiect the dlyes stability.
- Anhydrous alkali metal carbonates, and anhydrous borax are examples of suitable mildly alkaline-reacting water-soluble substances.
- the amount of mildly alkaline-reacting substance employed is preferably such that a pH of 7 to about 10 is obtained when the composition is brought into contact with water in the dyeing procedure.
- Some basic dyes as commercially available contain acid fillers, which require to be neutralised; with these dyes it is usually convenient to employ an amount of alkaline-reacting substance equal in weight to that of the dye, as in Example 2 below, so as to ensure the obtaining of the preferred pH subsequently.
- the composition can contain perfume, and also an inert filler to provide a suitable bulk.
- Suitable inert fillers are calcium carbonate, talc and anhydrous sodium sulphate.
- the powdered basic dye suitably forms from 2 to 40% by weight of the total composition, but concentrations well outside this range may be used, depending upon the condition and colour of the hair to be treated and on the intensity of colouration which it is desired to produce.
- the powdered basic dyes commercially available are generally useable direct (that is, without further subdivision) in preparing compositions according to the invention.
- the invention can be applied to the formulation of hair dye compositions from a wide variety of basic dyes used either singly, or mixed with one another or with other dyes, particularly disperse dyes, according to the colouration which it is desired to impart to the hair.
- said dyes should not be included, for they are incompatible with basic dyes.
- Suitable basic dyes are Meldolas Blue (Colour Index No. 51175), Ethyl Violet (Colour Index No. 42600), Malachite Green (Colour Index No. 42000), Para Rosaniline (Colour Index No. 42500), Rhodamine B (Colour Index No. 45170), Capri Blue GN (L) (Colour Index No. 51000), Methylene Blue (Colour Index No. 52015), Indolenine Yellow (Colour Index No. 48010), Crystal Violet (Colour Index 42555).
- compositions of the invention can be applied direct to wetted greasy hair, that is, without a preliminary washing to remove the grease.
- compositions of the invention are in general noncorrosive to metals, and accordingly those that are in paste form can be marketed in collapsible aluminum tubes having no protective internal coating.
- the liquid compositions can be marketed in bottles or in sachets of the usual kind.
- Example 2 *The grade employed here and in Example 2 was water'- white, and had specific gravity 0.858 at 60 F. and Redwood viscosIi ties 120 to 130 seconds at 70 F., 65 to 70 seconds at 100 The composition thus formed was found to be substantially unfaded after a years storage in a closed container.
- the paste composition was used as follows: 5 grams of the composition were mixed into a smooth paste with 42 grams of water, and the aqueous mixture (pH about 8) was applied in the usual manner to a head of greying Negro hair, on which it was allowed to remain for 20 minutes, The hair was then thoroughly washed ot remove surplus dye.
- This composition can be used in the manner described in Example 1. When applied to a head of greying hair for 20 minutes it produced an attractive amethyst shade.
- a hair dye composition in the form of a viscous mixture comprising powdered basic dye, a water-immiscible paraflinic hydrocarbon oil of Redwood viscosity greater than about seconds at 70 F., a surface-active agent selected from the class consisting of cationic and non-ionic surface-active agents, and a mildly alkalinereacting water-soluble substance selected from the class consisting of anhydrous alkali metal carbonates and anhydrous borax, the composition containing about 2% to 40% by Weight of the basic dye and the basic dye being substantially insoluble in the water-immiscible medium, said composition being substantially anhydrous.
- a hair dye composition in the form of a viscous A References Cited UNITED STATES PATENTS 1,594,490 8/1926 Bertolet 894 1,996,391 4/1935 Straus 4459 X 2,087,597 7/1937 Gutzeit 4459 2,114,370 4/1938 Bickenheuser 167-58 2,306,863 12/1942 Bour 86 X 3,086,914 4/1963 Soloway -167-88 X FOREIGN PATENTS 723,290 1/ 1932 France.
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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)
- Cosmetics (AREA)
Description
United States Patent ()ilfice Patented Feb. 20, 1968 3,369,970 DYEING HUMAN HAIR Terence P. McLaughlin, Twickenham and John B. Wilkinson, Hampton, England, assignors to Lever Brothers Company, New York, N.Y., a corporation of Maine No Drawing. Continuation-impart of application Ser. No. 486,222, Sept. 9, 1965. This application Nov. 10, 1966, Ser. No. 593,581 Claims priority, application Great Britain, Aug. 20, 1959, 28,459/ 59 3 Claims. (Cl. 167-88) ABSTRACT OF THE DISCLOSURE This specification is concerned with a hair dye composition which is a substantially anhydrous viscous mixture of a powdered basic dye and a water-immiscible 011.
This is a continuation-in-part of application Ser. No. 486,222 filed on Sept. 9, 1965, which in turn is a continuation of application Ser. No. 49,843 filed on Aug. 16, 1960. Both of the aforementioned applications are now abandoned.
This invention relates to the dyeing of human hair.
Hair dyeing with synthethic dyes is usually performed by applying either disperse dyes or the so-called oxida-.
tion dyes (which are oxidised to a dye proper while in contact with the hair) to the hair from an aqueous medium. However, oxidation dyes have the disadvantage that they are allergens, and have to be used with great care; and disperse dyes generally produce a hair colouration that tends to be rather easily removable by washing.
We have investigated the use of basic dyes for dyeing hair. Basic dyes are a well-known class of dyes which are used in dyeing wool and cotton and in which that part of the dye molecule which confers colour and fibre aflinity (substantivity) on the whole is a cation, in particular an ammonium, sulphonium or oxonium cation. Such dyes have marked afi'inity for human hair when applied to it from an aqueous medium, and can be used safely to produce a hair colouration which is generally of greater permanence on washing than that imparted by disperse dyes. Moreover, many basic dyes produce a hair colouration of intensity approaching that given by oxidation dyes.
However, there is serious diificulty in putting basic dyes into a form marketable as a hair dye composition. For if they are sold dry, either alone or admixed with another ingredient such as a thickener, they may badly stain the users fingers when he mixes the dry composition with the water that is required for the dyeing procedure; while if they are sold already mixed with part of or all the required water, the composition has too short a storage life to be acceptable, owing to the instability of basic dyes in the presence of water. Basic dyes have a marked tendency to change in the presence of water to non-substantive materials, through destruction of the cationic charge as a result of the fusion of a hydroxyl ion, OH, with the dye cation; and the rate of this change, although usually low in comparison with that of preparative reactions, is yet high enough to be serious in compositions which are required to be storable for an extended period. Moreover, the change is accelerated if the hair dye composition is formulated with a mildly alkaline-reacting water-soluble substance, such as borax or sodium carbonate, to improve uniformity of distribution of the dye along the length of the hair filaments during the actual dyeing procedure. Thus, many basic-dye-based aqueous hair dye compositions prepared with the use of sodium carbonate fade seriously within a week of their preparation.
We have now found that hair dye compositions of a form convenient for use and of good storage life can be obtained from a basic dye by mixing the powdered y with substantially water-immiscible oil or grease into the form of a viscous liquid or paste. (By grease is mean a semi-solid material which readily flows under applied pressure, as lubricating grease does.) The basic dye remains in solid form in the oil or grease medium, since such dyes are substantially insoluble in water-immiscible materials. Surprisingly enough, when the composition is eventually incorporated in the aqueous medium from which the dye will be transferred to the hair, and dyeing is performed in the usual manner, transfer of the dye to the hair is not appreciable hindered by the water-immiscible oil or grease.
The invention thus provides a hair dye composition in the form of a substantially anhydrous viscous liquid or paste comprising a powdered basic dye mixed with a water-immiscible oil or grease.
The oil (which is suitably of Redwood viscosity greater than about seconds at 70 F.) or grease medium employed should of course be one that is non-toxic. The use of a hydrocarbon as the water-immiscible medium is much to be preferred, although vegetable or animal oils or greases (whose molecules contain oxygen) can be used if an anti-oxidant or other stabiliser is also incorporated to inhibit the development of rancidity in them. Ordinary petroleum jelly is a suitable hydrocarbon grease; and suitable oils are parafiinic hydrocarbon oils such as refined light paraffin oil and medicinal parafiin.
Basic dyes, like disperse dyes and oxidation dyes, are applied to the hair from an aqueous medium in the presence of a surface-active agent, whose function is to reduce the natural water-repellency of hair and so facilitate intimate contact of the aqueous medium with the hair. It will usually be convenient to incorporate the surfaceactive agent in the composition itself, and for this purpose a cationic or non-ionic surface-active agent may be used. Anionic surface-active agents are not compatible with the basic dye. Suitable cationic surface-active agents are long chain alkyl quaternary ammonium salts, such as cetyltrimethylammonium bromide, tetradecyltrimethylammonium chloride, laurylpyridinium bromide, tetradecylpyridinium chloride and stearyldimethylbenzylammonium chloride; and suitable non-ionic surface-active agents are long chain alkanolamides, such as lauric acid diethanolamide, and the condensation products of ethylene oxide or propylene oxide with a compound containing a long chain alkyl group and an active hydrogen atom, for example, the condensation product of nonylphenol with from 10 to 15 molar proportions of ethylene oxide. Incorporating a surface-active agent in a composition containing an oil (liquid) as distinct from a grease (semi-solid) has the further advantage of reducing the tendency of the dye particles to partly separate out from the oil ingredient on prolonged storage.
The proportion of surface-active agent employed depends on whether the composition is intended to be applied direct to wetted hair or to be diluted with water immediately before application; a higher proportion will be required in the latter instance, in order to disperse the oil or grease medium in the larger volume of Water. In general, the surface-active agent suitably forms from 2 to 25% by Weight of the composition.
A thickener compatible with the dye is preferably incorporated in the composition, so that when the composition is brought into contact with water the aqueous mixture formed is sufficiently viscous to be worked about on the head without draining unduly quickly from it. Methyl cellulose is very satisfactory for the purpose. The proportion of thickener employed will be less when the composition is one intended for application direct to wetted hair than when the composition is to be diluted with water before being applied to the hair. In general, the thickener suitably forms from 1 to 25% by weight of the composition.
A mildly alkaline-reacting water-soluble substance can be incorporated in the composition, to improve distribution of the dye between the tips and roots of the hair during the dyeing procedure. Such substances are insoluble in the waterimmiscib1e oil or grease. Like the other ingredients of the composition, the alkaline-reacting substance should be substantially water-free, for even 1% of weight of water in the composition will normally serious- 13 afiect the dlyes stability. Anhydrous alkali metal carbonates, and anhydrous borax, are examples of suitable mildly alkaline-reacting water-soluble substances.
The amount of mildly alkaline-reacting substance employed is preferably such that a pH of 7 to about 10 is obtained when the composition is brought into contact with water in the dyeing procedure. Some basic dyes as commercially available contain acid fillers, which require to be neutralised; with these dyes it is usually convenient to employ an amount of alkaline-reacting substance equal in weight to that of the dye, as in Example 2 below, so as to ensure the obtaining of the preferred pH subsequently.
The composition can contain perfume, and also an inert filler to provide a suitable bulk. Suitable inert fillers are calcium carbonate, talc and anhydrous sodium sulphate.
.The powdered basic dye suitably forms from 2 to 40% by weight of the total composition, but concentrations well outside this range may be used, depending upon the condition and colour of the hair to be treated and on the intensity of colouration which it is desired to produce. The powdered basic dyes commercially available are generally useable direct (that is, without further subdivision) in preparing compositions according to the invention.
The invention can be applied to the formulation of hair dye compositions from a wide variety of basic dyes used either singly, or mixed with one another or with other dyes, particularly disperse dyes, according to the colouration which it is desired to impart to the hair. However, said dyes should not be included, for they are incompatible with basic dyes.
Suitable basic dyes, among others, are Meldolas Blue (Colour Index No. 51175), Ethyl Violet (Colour Index No. 42600), Malachite Green (Colour Index No. 42000), Para Rosaniline (Colour Index No. 42500), Rhodamine B (Colour Index No. 45170), Capri Blue GN (L) (Colour Index No. 51000), Methylene Blue (Colour Index No. 52015), Indolenine Yellow (Colour Index No. 48010), Crystal Violet (Colour Index 42555).
The compositions of the invention can be applied direct to wetted greasy hair, that is, without a preliminary washing to remove the grease.
The compositions of the invention are in general noncorrosive to metals, and accordingly those that are in paste form can be marketed in collapsible aluminum tubes having no protective internal coating. The liquid compositions can be marketed in bottles or in sachets of the usual kind.
The invention is illustrated by the following examples:
EXAMPLE 1 The following ingredients were mixed together in the stated weight proportions:
Meldolas Blue (No. 51175, The Colour Index,
2nd edition (1956), volume 3, page 3429) Anhydrous Borax 30 Refined parafiin oil 30 Cetyltrimethylammonium bromide 10 Methyl cellulose 14.5 Perfume 0.5
*The grade employed here and in Example 2 was water'- white, and had specific gravity 0.858 at 60 F. and Redwood viscosIi ties 120 to 130 seconds at 70 F., 65 to 70 seconds at 100 The composition thus formed was found to be substantially unfaded after a years storage in a closed container.
The paste composition was used as follows: 5 grams of the composition were mixed into a smooth paste with 42 grams of water, and the aqueous mixture (pH about 8) was applied in the usual manner to a head of greying Negro hair, on which it was allowed to remain for 20 minutes, The hair was then thoroughly washed ot remove surplus dye.
The hair was found to have acquired an intense blueblack shade. It had an attractive gloss, and its colouration was stable to washing.
EXAMPLE 2 The following ingredients were mixed together in the stated weight proportions:
Ethyl Violet (No. 42600, The Colour Index,
2nd edition (1956), volume 3, page 3360) 7 Anhydrous borax 35 Refined paraffin oil 33.5 Cetyltrimethylammonium bromide 10 Methyl cellulose 14 Perfume 0.5
This composition can be used in the manner described in Example 1. When applied to a head of greying hair for 20 minutes it produced an attractive amethyst shade.
What is claimed is:
1. A hair dye composition in the form of a viscous mixture comprising powdered basic dye, a water-immiscible paraflinic hydrocarbon oil of Redwood viscosity greater than about seconds at 70 F., a surface-active agent selected from the class consisting of cationic and non-ionic surface-active agents, and a mildly alkalinereacting water-soluble substance selected from the class consisting of anhydrous alkali metal carbonates and anhydrous borax, the composition containing about 2% to 40% by Weight of the basic dye and the basic dye being substantially insoluble in the water-immiscible medium, said composition being substantially anhydrous.
2. A hair dye composition according to claim 1, in which the oil is refined light paraffin oil.
3. A hair dye composition in the form of a viscous A References Cited UNITED STATES PATENTS 1,594,490 8/1926 Bertolet 894 1,996,391 4/1935 Straus 4459 X 2,087,597 7/1937 Gutzeit 4459 2,114,370 4/1938 Bickenheuser 167-58 2,306,863 12/1942 Bour 86 X 3,086,914 4/1963 Soloway -167-88 X FOREIGN PATENTS 723,290 1/ 1932 France.
OTHER REFERENCES Pharmaceutical Formulas, vol. I, The Chemist and Druggist, London, England, 1944, p. 681.
ALBERT T. MEYERS, Primary Examiner.
VERA C. CLARKE, Assistant Examiner.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB28459/59A GB880798A (en) | 1959-08-20 | 1959-08-20 | Compositions for dyeing human hair |
Publications (1)
Publication Number | Publication Date |
---|---|
US3369970A true US3369970A (en) | 1968-02-20 |
Family
ID=10275961
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US593581A Expired - Lifetime US3369970A (en) | 1959-08-20 | 1966-11-10 | Dyeing human hair |
Country Status (5)
Country | Link |
---|---|
US (1) | US3369970A (en) |
CH (1) | CH389163A (en) |
DE (1) | DE1139607B (en) |
ES (1) | ES260485A1 (en) |
GB (1) | GB880798A (en) |
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US3515598A (en) * | 1966-10-27 | 1970-06-02 | Durand & Huguenin Ag | Stable preparation for the production of prints on an oxide film artificially produced on aluminum |
US4096243A (en) * | 1976-02-09 | 1978-06-20 | Clairol Incorporated | Composition for lightening hair containing an oxidizing agent and certain quaternary amines |
US4168144A (en) * | 1970-11-06 | 1979-09-18 | Lever Brothers Company | Keratinous fibers colorant compositions containing basic dyes and an anionic-cationic detergent complex |
US4184843A (en) * | 1976-08-31 | 1980-01-22 | Carl Viktor Danielson | Composition for dyeing hair containing disperse dyes and a thickening agent |
US4402700A (en) * | 1976-02-09 | 1983-09-06 | Clairol Incorporated | Composition for coloring hair containing an oxidizing agent and certain quaternary amines |
US4532127A (en) * | 1976-02-09 | 1985-07-30 | Clairol Incorporated | Composition for lightening or coloring hair containing an oxidizing agent and certain quaternary amines |
US5865853A (en) * | 1996-05-09 | 1999-02-02 | Wella Aktiengesellschaft | Composition for dyeing keratin fibers containing vegetable dyes, a direct dye compound and oil and method of dyeing hair using same |
US20040083560A1 (en) * | 2001-03-08 | 2004-05-06 | Jean-Marie Adam | Method of clouring porous material |
US20050235433A1 (en) * | 1998-07-09 | 2005-10-27 | L'oreal S.A. | Composition for dyeing keratin fibers with a cationic direct dye and a thickening polymer |
WO2006136518A2 (en) | 2005-06-23 | 2006-12-28 | Ciba Specialty Chemicals Holding Inc. | Nitrosulfide dyes |
WO2007025889A2 (en) | 2005-08-30 | 2007-03-08 | Ciba Specialty Chemicals Holding Inc. | Dyes containing a thiol group |
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US20090158533A1 (en) * | 2007-12-21 | 2009-06-25 | Leila Hercouet | Method for dyeing in the presence of at least one oxidizing agent and at least one organic amine, device for use thereof and ready-to-use composition |
US20090162309A1 (en) * | 2007-12-21 | 2009-06-25 | Leila Hercouet | Method for lightening human keratin fibers using at least one anhydrous composition, at least one organic amine, and at least one oxidizing agent, and device for use thereof |
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US20100154139A1 (en) * | 2008-12-19 | 2010-06-24 | Giafferi Marie | Composition for the oxidation dyeing of keratin fibers comprising para-aminophenol, dipropylene glycol and at least one additional dye precursor |
US20100158844A1 (en) * | 2008-12-19 | 2010-06-24 | Damarys Braida-Valerio | Oxidizing composition for the treatment of keratin fibers comprising at least one oil, atleast one fatty alcohol and at least one oxyalkylenated fatty alcohol |
US20100154136A1 (en) * | 2008-12-19 | 2010-06-24 | Hercouet Leila | Composition comprising at least one fatty substance and at least one cationic polymer, dyeing or lightening process using it and devices therefor |
US20100154137A1 (en) * | 2008-12-19 | 2010-06-24 | Hercouet Leila | Method of coloring or lightening in the presence of an inorganic base and kit |
US20100154142A1 (en) * | 2008-12-19 | 2010-06-24 | Marie-Pascale Audousset | Composition for the oxidation dyeing of keratin fibers comprising at least one fatty substance and at least one N,N-bis(beta-hydroxyethyl)-para-phenylenediamine |
US20100154141A1 (en) * | 2008-12-19 | 2010-06-24 | Hercouet Leila | Process for the lightening dyeing of keratin materials using an emulsion comprising a dye and an alkaline agent and an oxidizing composition |
US20100154140A1 (en) * | 2008-12-19 | 2010-06-24 | Simonet Frederic | Ready-to-use composition for oxidation dyeing of keratin fibers comprising at least one fatty substance, at least one thickener, at least one dye precursor, at least one oxidizing agent, and at least one alkaline agent, and process and kits therewith |
US20100158839A1 (en) * | 2008-12-19 | 2010-06-24 | Damarys Braida-Valerio | Oxidizing composition for the treatment of keratin fibers comprising at least one cationic polymer, at least one fatty amide and at least one anti-oxygen agent |
FR2940052A1 (en) * | 2008-12-19 | 2010-06-25 | Oreal | Composition, useful for dyeing keratin fibers, preferably human hair, comprises fatty substance, surfactants and two reactive compounds capable of generating all colored species in the absence of any chemical oxidant |
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US20100162492A1 (en) * | 2008-12-19 | 2010-07-01 | Hercouet Leila | Ready-to-use composition for oxidation dyeing of keratin fibers comprising at least one fatty substance chosen from fatty amides and fatty acid esters, at least one dye precursor, at least one oxidizing agent and optionally at least one alkaline agent, and methods and kits therewith |
US20100166688A1 (en) * | 2008-12-19 | 2010-07-01 | Hercouet Leila | Process for lightening keratin materials using an emulsion comprising an alkaline agent and an oxidizing composition |
US20100162493A1 (en) * | 2008-12-19 | 2010-07-01 | Marie-Pascale Audousset | Composition for oxidation dyeing of keratin fibers comprising at least one fatty substance, at least one oxidation base, at least one dye precursor, at least one oxidizing agent, and optionally at least one alkaline agent, and processes and kits therewith |
US20100175705A1 (en) * | 2008-12-19 | 2010-07-15 | Hercouet Leila | Process for lightening or lightening direct dyeing or oxidation dyeing in the presence of at least one organic amine and at least one inorganic base, and device therefor |
US20100175706A1 (en) * | 2008-12-19 | 2010-07-15 | Hercouet Leila | Process for dyeing or lighten human keratin fibers using an anhydrous composition and a monoethyanolamine/basic amino acid mixture, and suitable device therefor |
US20100175202A1 (en) * | 2008-12-19 | 2010-07-15 | Simonet Frederic | Composition comprising at least one fatty substance and at least one silicate, dyeing or lightening process using it and devices or kits therefor |
US20100178263A1 (en) * | 2008-12-19 | 2010-07-15 | Simonet Frederic | Process for lightening keratin materials using an anhydrous composition comprising at least one fatty substance and at least one alkaline agent, and at least one oxidizing composition |
US20100178264A1 (en) * | 2008-12-19 | 2010-07-15 | Hercouet Leila | Process for lightening or process for direct dyeing or oxidation dyeing of keratin fibers in the presence of at least one ammonium salt and device therefor |
US20100180389A1 (en) * | 2008-12-19 | 2010-07-22 | Leila Hercouet | Composition comprising at least one fatty substance and at least one surfactant comprising ethylene oxide, dyeing or lightening process using it and devices therefor |
US20100199441A1 (en) * | 2008-12-19 | 2010-08-12 | Hercouet Leila | Lightening and dyeing of human keratin fibers using an anhydrous composition comprising a monoethyanolamine/basic amino acid mixture, and device therefor |
WO2010097339A2 (en) | 2009-02-25 | 2010-09-02 | Basf Se | Hair dyeing composition |
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US20100223739A1 (en) * | 2008-12-19 | 2010-09-09 | Hercouet Leila | Process for lightening or lightening direct dyeing or oxidation dyeing in the presence of an aqueous composition comprising at least one fatty substance, and device |
FR2944440A1 (en) * | 2008-12-19 | 2010-10-22 | Oreal | Composition, useful for dyeing human keratin fibers, comprises fatty substance, and auto-oxidizable dyes in a medium |
WO2011006946A2 (en) | 2009-07-15 | 2011-01-20 | Basf Se | Polymeric hair dyes |
US7901464B2 (en) | 2007-12-21 | 2011-03-08 | L'oreal S.A. | Process for lightening direct dyeing or oxidation dyeing in the presence of at least one organic amine, device therefor and anhydrous composition |
US7927382B2 (en) | 2008-12-19 | 2011-04-19 | L'oreal S.A. | Ready-to-use composition for the oxidation dyeing of keratin fibers comprising at least one fatty substance, at least one oxidation chosen from 4,5-diaminopyrazoles and acid addition salts thereof, at least one additional dye precursor other than the at least one oxidation base, at least one oxidizing agent, and optionally at least one alkaline agent, and processes and kits therewith |
US20110155167A1 (en) * | 2009-12-22 | 2011-06-30 | Gautier Deconinck | Agent for dyeing and/or bleaching keratin fibers in two parts, comprising at least one fatty substance and at least one sequestrant |
US20110158925A1 (en) * | 2009-12-22 | 2011-06-30 | Jean-Marc Ascione | Dyeing or lightening compositions comprising at least one fatty substance and at least one amphoteric polymer |
US20110155166A1 (en) * | 2009-12-22 | 2011-06-30 | Gautier Deconinck | Agent for dyeing and/or bleaching keratin fibers, comprising composition (a), anhydrous composition (b), and at least one fatty substance |
US20110232667A1 (en) * | 2008-12-19 | 2011-09-29 | Hercouet Leila | Hair treatment process using a direct emulsion comprising an oxidizing agent and a composition containing an alkaline agent |
US8070831B2 (en) | 2008-12-19 | 2011-12-06 | L'oreal S.A. | Composition comprising at least one solid fatty alcohol, dyeing or lightening process using same and devices |
US8114170B2 (en) | 2009-12-22 | 2012-02-14 | L'oreal S.A. | Agent for coloring and/or bleaching keratin fibers comprising composition (A), composition (B), at least one fat and at least one reductone |
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WO2015028543A1 (en) | 2013-09-02 | 2015-03-05 | Basf Se | Styryl sulfide dyes |
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DE69821324T2 (en) * | 1997-12-05 | 2004-11-18 | L'oreal | Two-step process for the direct dyeing of keratin fibers using basic direct dyes |
JP2002012533A (en) * | 2000-06-27 | 2002-01-15 | Kao Corp | Hair dye composition |
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Cited By (85)
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US3515598A (en) * | 1966-10-27 | 1970-06-02 | Durand & Huguenin Ag | Stable preparation for the production of prints on an oxide film artificially produced on aluminum |
US4168144A (en) * | 1970-11-06 | 1979-09-18 | Lever Brothers Company | Keratinous fibers colorant compositions containing basic dyes and an anionic-cationic detergent complex |
US4096243A (en) * | 1976-02-09 | 1978-06-20 | Clairol Incorporated | Composition for lightening hair containing an oxidizing agent and certain quaternary amines |
US4119399A (en) * | 1976-02-09 | 1978-10-10 | Clairol Incorporated | Composition for coloring hair containing an oxidizing agent and certain quaternary amines |
US4402700A (en) * | 1976-02-09 | 1983-09-06 | Clairol Incorporated | Composition for coloring hair containing an oxidizing agent and certain quaternary amines |
US4532127A (en) * | 1976-02-09 | 1985-07-30 | Clairol Incorporated | Composition for lightening or coloring hair containing an oxidizing agent and certain quaternary amines |
US4184843A (en) * | 1976-08-31 | 1980-01-22 | Carl Viktor Danielson | Composition for dyeing hair containing disperse dyes and a thickening agent |
US5865853A (en) * | 1996-05-09 | 1999-02-02 | Wella Aktiengesellschaft | Composition for dyeing keratin fibers containing vegetable dyes, a direct dye compound and oil and method of dyeing hair using same |
US20070006396A9 (en) * | 1998-07-09 | 2007-01-11 | L'oreal S.A. | Composition for dyeing keratin fibers with a cationic direct dye and a thickening polymer |
US20050235433A1 (en) * | 1998-07-09 | 2005-10-27 | L'oreal S.A. | Composition for dyeing keratin fibers with a cationic direct dye and a thickening polymer |
US7041143B2 (en) | 2001-03-08 | 2006-05-09 | Ciba Specialty Chemicals Corporation | Method of coloring porous material |
US20040083560A1 (en) * | 2001-03-08 | 2004-05-06 | Jean-Marie Adam | Method of clouring porous material |
EP2075036A1 (en) | 2004-04-08 | 2009-07-01 | Ciba Holding Inc. | Disulfid dyes, composition comprising them and method of dyeing hair |
WO2006136518A2 (en) | 2005-06-23 | 2006-12-28 | Ciba Specialty Chemicals Holding Inc. | Nitrosulfide dyes |
WO2007025889A2 (en) | 2005-08-30 | 2007-03-08 | Ciba Specialty Chemicals Holding Inc. | Dyes containing a thiol group |
WO2007144280A2 (en) | 2006-06-13 | 2007-12-21 | Ciba Holding Inc. | Tricationic dyes |
US20090158533A1 (en) * | 2007-12-21 | 2009-06-25 | Leila Hercouet | Method for dyeing in the presence of at least one oxidizing agent and at least one organic amine, device for use thereof and ready-to-use composition |
US20090162309A1 (en) * | 2007-12-21 | 2009-06-25 | Leila Hercouet | Method for lightening human keratin fibers using at least one anhydrous composition, at least one organic amine, and at least one oxidizing agent, and device for use thereof |
US9005594B2 (en) | 2007-12-21 | 2015-04-14 | L'oreal | Method for lightening human keratin fibers using at least one anhydrous composition, at least one organic amine, and at least one oxidizing agent, and device for use thereof |
US7909887B2 (en) | 2007-12-21 | 2011-03-22 | L'oreal S.A. | Method for dyeing in the presence of at least one oxidizing agent and at least one organic amine, device for use thereof and ready-to-use composition |
US7901464B2 (en) | 2007-12-21 | 2011-03-08 | L'oreal S.A. | Process for lightening direct dyeing or oxidation dyeing in the presence of at least one organic amine, device therefor and anhydrous composition |
WO2009090125A1 (en) | 2008-01-17 | 2009-07-23 | Basf Se | Polymeric hair dyes |
FR2944440A1 (en) * | 2008-12-19 | 2010-10-22 | Oreal | Composition, useful for dyeing human keratin fibers, comprises fatty substance, and auto-oxidizable dyes in a medium |
US7927381B2 (en) | 2008-12-19 | 2011-04-19 | L'oreal S.A. | Process for lightening or lightening direct dyeing or oxidation dyeing in the presence of an aqueous composition comprising at least one fatty substance, and device |
US20100154141A1 (en) * | 2008-12-19 | 2010-06-24 | Hercouet Leila | Process for the lightening dyeing of keratin materials using an emulsion comprising a dye and an alkaline agent and an oxidizing composition |
US20100154140A1 (en) * | 2008-12-19 | 2010-06-24 | Simonet Frederic | Ready-to-use composition for oxidation dyeing of keratin fibers comprising at least one fatty substance, at least one thickener, at least one dye precursor, at least one oxidizing agent, and at least one alkaline agent, and process and kits therewith |
US20100158839A1 (en) * | 2008-12-19 | 2010-06-24 | Damarys Braida-Valerio | Oxidizing composition for the treatment of keratin fibers comprising at least one cationic polymer, at least one fatty amide and at least one anti-oxygen agent |
FR2940052A1 (en) * | 2008-12-19 | 2010-06-25 | Oreal | Composition, useful for dyeing keratin fibers, preferably human hair, comprises fatty substance, surfactants and two reactive compounds capable of generating all colored species in the absence of any chemical oxidant |
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US20100162492A1 (en) * | 2008-12-19 | 2010-07-01 | Hercouet Leila | Ready-to-use composition for oxidation dyeing of keratin fibers comprising at least one fatty substance chosen from fatty amides and fatty acid esters, at least one dye precursor, at least one oxidizing agent and optionally at least one alkaline agent, and methods and kits therewith |
US20100166688A1 (en) * | 2008-12-19 | 2010-07-01 | Hercouet Leila | Process for lightening keratin materials using an emulsion comprising an alkaline agent and an oxidizing composition |
US20100162493A1 (en) * | 2008-12-19 | 2010-07-01 | Marie-Pascale Audousset | Composition for oxidation dyeing of keratin fibers comprising at least one fatty substance, at least one oxidation base, at least one dye precursor, at least one oxidizing agent, and optionally at least one alkaline agent, and processes and kits therewith |
US20100175705A1 (en) * | 2008-12-19 | 2010-07-15 | Hercouet Leila | Process for lightening or lightening direct dyeing or oxidation dyeing in the presence of at least one organic amine and at least one inorganic base, and device therefor |
US20100175706A1 (en) * | 2008-12-19 | 2010-07-15 | Hercouet Leila | Process for dyeing or lighten human keratin fibers using an anhydrous composition and a monoethyanolamine/basic amino acid mixture, and suitable device therefor |
US20100175202A1 (en) * | 2008-12-19 | 2010-07-15 | Simonet Frederic | Composition comprising at least one fatty substance and at least one silicate, dyeing or lightening process using it and devices or kits therefor |
US20100178263A1 (en) * | 2008-12-19 | 2010-07-15 | Simonet Frederic | Process for lightening keratin materials using an anhydrous composition comprising at least one fatty substance and at least one alkaline agent, and at least one oxidizing composition |
US20100178264A1 (en) * | 2008-12-19 | 2010-07-15 | Hercouet Leila | Process for lightening or process for direct dyeing or oxidation dyeing of keratin fibers in the presence of at least one ammonium salt and device therefor |
US20100180389A1 (en) * | 2008-12-19 | 2010-07-22 | Leila Hercouet | Composition comprising at least one fatty substance and at least one surfactant comprising ethylene oxide, dyeing or lightening process using it and devices therefor |
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US20100199441A1 (en) * | 2008-12-19 | 2010-08-12 | Hercouet Leila | Lightening and dyeing of human keratin fibers using an anhydrous composition comprising a monoethyanolamine/basic amino acid mixture, and device therefor |
US11691035B2 (en) | 2008-12-19 | 2023-07-04 | L'oreal | Oxidizing composition for the treatment of keratin fibers comprising at least one cationic polymer, at least one fatty amide and at least one anti-oxygen agent |
US9017424B2 (en) | 2008-12-19 | 2015-04-28 | L'oreal | Process for lightening keratin materials using an emulsion comprising an alkaline agent and an oxidizing composition |
US20100223739A1 (en) * | 2008-12-19 | 2010-09-09 | Hercouet Leila | Process for lightening or lightening direct dyeing or oxidation dyeing in the presence of an aqueous composition comprising at least one fatty substance, and device |
US20100154137A1 (en) * | 2008-12-19 | 2010-06-24 | Hercouet Leila | Method of coloring or lightening in the presence of an inorganic base and kit |
US20100154139A1 (en) * | 2008-12-19 | 2010-06-24 | Giafferi Marie | Composition for the oxidation dyeing of keratin fibers comprising para-aminophenol, dipropylene glycol and at least one additional dye precursor |
US7879113B2 (en) | 2008-12-19 | 2011-02-01 | L'oreal S.A. | Composition comprising at least one fatty substance and at least one silicate, dyeing or lightening process using it and devices or kits therefor |
US20100154136A1 (en) * | 2008-12-19 | 2010-06-24 | Hercouet Leila | Composition comprising at least one fatty substance and at least one cationic polymer, dyeing or lightening process using it and devices therefor |
US20100158844A1 (en) * | 2008-12-19 | 2010-06-24 | Damarys Braida-Valerio | Oxidizing composition for the treatment of keratin fibers comprising at least one oil, atleast one fatty alcohol and at least one oxyalkylenated fatty alcohol |
US7909888B2 (en) | 2008-12-19 | 2011-03-22 | L'oreal | Process for dyeing or lightening human keratin fibers using an anhydrous composition and a monoethanolamine/basic amino acid mixture, and suitable device therefor |
US7914591B2 (en) | 2008-12-19 | 2011-03-29 | L'oreal S.A. | Process for the lightening dyeing of keratin materials using at least one anhydrous dyeing composition comprising at least one alkaline agent and at least one oxidizing composition |
US7918903B2 (en) | 2008-12-19 | 2011-04-05 | L'oreal, S.A. | Composition for the oxidation dyeing of keratin fibers comprising at least one fatty substance and at least one N,N bis(beta-hydroxyethyl)-para-phenylenediamine |
US7918902B2 (en) | 2008-12-19 | 2011-04-05 | L'oreal S.A. | Process for lightening or process for direct dyeing or oxidation dyeing of keratin fibers in the presence of at least one ammonium salt and device therefor |
US7922777B2 (en) | 2008-12-19 | 2011-04-12 | L'ORéAL S.A. | Lightening and dyeing of human keratin fibers using an anhydrous composition comprising a monoethyanolamine/basic amino acid mixture, and device therefor |
US20100154142A1 (en) * | 2008-12-19 | 2010-06-24 | Marie-Pascale Audousset | Composition for the oxidation dyeing of keratin fibers comprising at least one fatty substance and at least one N,N-bis(beta-hydroxyethyl)-para-phenylenediamine |
US7927382B2 (en) | 2008-12-19 | 2011-04-19 | L'oreal S.A. | Ready-to-use composition for the oxidation dyeing of keratin fibers comprising at least one fatty substance, at least one oxidation chosen from 4,5-diaminopyrazoles and acid addition salts thereof, at least one additional dye precursor other than the at least one oxidation base, at least one oxidizing agent, and optionally at least one alkaline agent, and processes and kits therewith |
US7927380B2 (en) | 2008-12-19 | 2011-04-19 | L'oreal S.A. | Composition for oxidation dyeing of keratin fibers comprising at least one fatty substance, at least one oxidation base, at least one dye precursor, at least one oxidizing agent, and optionally at least one alkaline agent, and processes and kits therewith |
US7927383B2 (en) | 2008-12-19 | 2011-04-19 | L'oreal S.A. | Composition comprising at least one fatty substance and at least one surfactant comprising ethylene oxide, dyeing or lightening process using it and devices therefor |
US7931698B2 (en) | 2008-12-19 | 2011-04-26 | L'oreal S.A. | Ready-to-use composition for oxidation dyeing of keratin fibers comprising at least one fatty substance, at least one thickener, at least one dye precursor, at least one oxidizing agent, and at least one alkaline agent, and process and kits therewith |
US7935154B2 (en) | 2008-12-19 | 2011-05-03 | L'oreal S.A. | Process for lightening or lightening direct dyeing or oxidation dyeing in the presence of at least one organic amine and at least one inorganic base, and device therefor |
US7947089B2 (en) | 2008-12-19 | 2011-05-24 | L'oreal S.A. | Method of coloring or lightening in the presence of an inorganic base and kit |
US8889110B2 (en) | 2008-12-19 | 2014-11-18 | L'oreal | Oxidizing composition for the treatment of keratin fibers comprising at least one oil, at least one fatty alcohol and at least one oxyalkylenated fatty alcohol |
US8262739B2 (en) | 2008-12-19 | 2012-09-11 | L'oreal S.A. | Hair treatment process using a direct emulsion comprising an oxidizing agent and a composition containing an alkaline agent |
US8092553B2 (en) | 2008-12-19 | 2012-01-10 | L'oreal S.A. | Composition for the oxidation dyeing of keratin fibers comprising para-aminophenol, dipropylene glycol and at least one additional dye precursor |
US7981165B2 (en) | 2008-12-19 | 2011-07-19 | L'oreal S.A. | Process for lightening keratin materials using an anhydrous composition comprising at least one fatty substance and at least one alkaline agent, and at least one oxidizing composition |
US7988738B2 (en) | 2008-12-19 | 2011-08-02 | L'oreal S.A. | Process for the lightening dyeing of keratin materials using an emulsion comprising a dye and an alkaline agent and an oxidizing composition |
US7988737B2 (en) | 2008-12-19 | 2011-08-02 | L'oreal S.A. | Ready-to-use composition for oxidation dyeing of keratin fibers comprising at least one fatty substance chosen from fatty amides and fatty acid esters, at least one dye precursor, at least one oxidizing agent and optionally at least one alkaline agent, and methods and kits therewith |
US20110232667A1 (en) * | 2008-12-19 | 2011-09-29 | Hercouet Leila | Hair treatment process using a direct emulsion comprising an oxidizing agent and a composition containing an alkaline agent |
US8066781B2 (en) | 2008-12-19 | 2011-11-29 | L'oreal S.A. | Composition comprising at least one fatty substance and at least one cationic polymer, dyeing or lightening process using it and devices therefor |
US8070831B2 (en) | 2008-12-19 | 2011-12-06 | L'oreal S.A. | Composition comprising at least one solid fatty alcohol, dyeing or lightening process using same and devices |
WO2010097338A2 (en) | 2009-02-25 | 2010-09-02 | Basf Se | Hair dyeing composition |
US8257448B2 (en) | 2009-02-25 | 2012-09-04 | Basf Se | Hair dyeing composition |
WO2010097339A2 (en) | 2009-02-25 | 2010-09-02 | Basf Se | Hair dyeing composition |
EP3459520A1 (en) | 2009-02-25 | 2019-03-27 | Basf Se | Hair dyeing composition |
US8268014B2 (en) | 2009-02-25 | 2012-09-18 | BASF SE Ludwigshafen | Hair dyeing composition |
WO2011006946A2 (en) | 2009-07-15 | 2011-01-20 | Basf Se | Polymeric hair dyes |
US20110155167A1 (en) * | 2009-12-22 | 2011-06-30 | Gautier Deconinck | Agent for dyeing and/or bleaching keratin fibers in two parts, comprising at least one fatty substance and at least one sequestrant |
US8114170B2 (en) | 2009-12-22 | 2012-02-14 | L'oreal S.A. | Agent for coloring and/or bleaching keratin fibers comprising composition (A), composition (B), at least one fat and at least one reductone |
US8147564B2 (en) | 2009-12-22 | 2012-04-03 | L'oreal | Agent for dyeing and/or bleaching keratin fibers, comprising composition (A), anhydrous composition (B), and at least one fatty substance |
US20110158925A1 (en) * | 2009-12-22 | 2011-06-30 | Jean-Marc Ascione | Dyeing or lightening compositions comprising at least one fatty substance and at least one amphoteric polymer |
US8142518B2 (en) | 2009-12-22 | 2012-03-27 | L'oreal | Agent for dyeing and/or bleaching keratin fibers in two parts, comprising at least one fatty substance and at least one sequestrant |
US20110155166A1 (en) * | 2009-12-22 | 2011-06-30 | Gautier Deconinck | Agent for dyeing and/or bleaching keratin fibers, comprising composition (a), anhydrous composition (b), and at least one fatty substance |
US8118884B2 (en) | 2009-12-22 | 2012-02-21 | L'oreal S.A. | Dyeing or lightening compositions comprising at least one fatty substance and at least one amphoteric polymer |
WO2012022709A1 (en) | 2010-08-17 | 2012-02-23 | Basf Se | Disulfide or thiol polymeric hair dyes |
WO2015028543A1 (en) | 2013-09-02 | 2015-03-05 | Basf Se | Styryl sulfide dyes |
US10047225B2 (en) | 2013-09-02 | 2018-08-14 | Basf Se | Styryl sulfide dyes |
Also Published As
Publication number | Publication date |
---|---|
DE1139607B (en) | 1962-11-15 |
CH389163A (en) | 1965-03-15 |
GB880798A (en) | 1961-10-25 |
ES260485A1 (en) | 1961-01-16 |
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