EP1082087A1 - Compositions et techniques afferentes de decoloration de fibres keratiniques colorees de maniere permanente - Google Patents

Compositions et techniques afferentes de decoloration de fibres keratiniques colorees de maniere permanente

Info

Publication number
EP1082087A1
EP1082087A1 EP99925931A EP99925931A EP1082087A1 EP 1082087 A1 EP1082087 A1 EP 1082087A1 EP 99925931 A EP99925931 A EP 99925931A EP 99925931 A EP99925931 A EP 99925931A EP 1082087 A1 EP1082087 A1 EP 1082087A1
Authority
EP
European Patent Office
Prior art keywords
bicarbonate
composition
dye
hair
hydrogen peroxide
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP99925931A
Other languages
German (de)
English (en)
Other versions
EP1082087A4 (fr
Inventor
Tony R. Adair
Donald R. Cowsar
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Carson Products Co
Original Assignee
Carson Products Co
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Carson Products Co filed Critical Carson Products Co
Publication of EP1082087A1 publication Critical patent/EP1082087A1/fr
Publication of EP1082087A4 publication Critical patent/EP1082087A4/fr
Withdrawn legal-status Critical Current

Links

Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/08—Preparations for bleaching the hair
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • 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
    • A61K8/19—Cosmetics or similar toiletry preparations characterised by the composition containing inorganic ingredients
    • A61K8/22—Peroxides; Oxygen; Ozone

Definitions

  • the present invention relates to the removal of color from dyed keratin fibers, such as human hair or wool, with compositions containing bicarbonate salts and hydrogen peroxide.
  • the present invention is capable of providing a degree of lift in previously dyed keratin fibers which, heretofore, has not been possible under mild reaction conditions. Further, the invention described herein is especially suitable for use on keratin fibers which were chemically treated prior to subsequent dyeing.
  • oxidative dyes to change the color of keratin fibers involves the use of hydrogen peroxide or an agent capable of producing hydrogen peroxide in solution, and small compounds, called dye intermediates.
  • the hydrogen peroxide is admixed with the dye intermediates just prior to application to the keratin fiber.
  • Hydrogen peroxide causes the small dye intermediates to couple inside the keratin fiber forming a large colored molecule. This colored molecule imparts color to the keratin fiber and is of sufficient size that it cannot diffuse out of the fiber without further chemical treatment.
  • a single oxidative dye treatment lasts from 10 to 30 minutes with the more customary treatments ranging in length from 20 min to 30 min. While fairly straight forward, this process is not without consequence.
  • the oxidizing agent in this example hydrogen peroxide, can also weaken the keratin fiber by attacking the proteins which give the hair it's structural integrity. In fact, a number of factors combine to determine whether or not the dyed fibers will be excessively damaged. These include the concentration of the oxidizing agent, the duration of the treatment, and most importantly the initial condition of the fiber. Those skilled in the art know that keratin fibers which have already been weakened by prior chemical or mechanical treatments, can be severely damaged, sometimes to the point of breakage, by treatment with oxidizing agents.
  • Human hair will be used as an example of such keratin fiber for demonstration purposes.
  • the importance of hair to the human psyche is evident by the multitude of different methods available for changing its appearance. Through the ages different methods of coloring, straightening, curling, and otherwise changing the appearance of the hair have been developed. While bleaching and coloring of hair are among the most widely practiced modifications to human hair today, other treatments are also used to obtain the desired "look”. Curly hair is physically or chemically straightened, and straight hair can be physically or chemically curled. Each of these treatments causes some weakening of the proteins which give hair its structural integrity and great care must be taken to minimize excessive damage to the fiber.
  • boosters which, when added to a bleaching composition containing hydrogen peroxide, remove dye molecules from keratin fibers.
  • the boosters of current art are typically salts of peroxy acids. Although percarbonates and perborates have been suggested as boosters for lifting hair, the most commonly employed boosters are persulfate salts.
  • persulfate salts are currently employed in dye removal compositions to provide a degree of lift in dyed hair in excess of that obtained when hydrogen peroxide and ammonia are used alone. These include ammonium persulfate, potassium persulfate, and sodium persulfate. Typically, these salts or blends of these salts are packaged separately from the hydrogen peroxide. In use, a packet of persulfate is added to the hydrogen peroxide immediately before the mixture is applied to the hair. Unfortunately, those skilled in the art also know that persulfates are among the most damaging oxidative agents which can be applied to the hair.
  • persulfate boosters to remove dye molecules from hair weakens the fiber because of uncontrolled side reactions with the proteins which give the fiber its structural integrity. Persulfates can be especially damaging to hair which has received a permanent wave or has been chemically straightened. Persulfate boosters also present many problems for the product manufacturer and the consumer as well.
  • Persulfates are very reactive oxidizing agents. This reactivity causes problems in the storage, handling and shipping of these materials. Manufacturers of hair color products often must rely on contract packagers for the preparation of booster packets. Those manufacturers who chose to prepare booster packets must invest a great deal of time, energy, and equipment in ensuring the safe handling and shipping of these materials. The end result of this effort is an increased cost of manufacturing for color-removal products which require a persulfate booster.
  • persulfate boosters tend to be irritating and even toxic if ingested.
  • the small packets of persulfate booster employed in the current art could easily be opened and ingested by children. Further, the opening of booster packets can cause the powdered persulfates to become airborne. Particles of persulfate boosters which come into contact with the eyes, skin, and mucous membranes can easily cause burns or inhalation-related illnesses.
  • persulfate boosters presents further problems in actual use.
  • the boosters of the current art are somewhat difficult to dissolve.
  • the mixture of hydrogen peroxide and these persulfate boosters must be shaken until the persulfates are fully dissolved.
  • the difficulty in dissolving persulfates causes excessive foaming of the product and builds up pressure inside the mixing vessel. Therefore, the violent, involuntary evolution of product from the container represents a possible health hazard to the user.
  • persulfate boosters often enhance the "chemical" odor of the finished blend making the color-removal treatment less pleasant for the consumer.
  • the inventors have discovered that a degree of dye removal comparable to and in some instances superior to that obtained with a persulfate booster/peroxide combinations can be obtained under relatively mild conditions using bicarbonate salts and hydrogen peroxide. Further, the inventors have discovered that the bicarbonate ion plays a major role in the decolorization of oxidative dye molecules in keratin fibers. Carbonate salts which are not comprised of a blend of bicarbonate and carbonate forms, do not provide the same degree of decolorization as is obtained with bicarbonates having the same cation.
  • the degree of decolorization provided by the use of said salt is proportional to the amount of the bicarbonate form present in the mixture.
  • This previously unknown and unsuspected attribute of bicarbonate ion provides for a relatively safe, natural, non-toxic booster for the removal of dye molecules from keratin fibers.
  • the present invention provides for the removal of dye molecules from keratin fibers under reaction conditions milder than those in which persulfates are used and is especially suitable for use on keratin fibers which have been weakened by prior chemical treatments.
  • the method and compositions of this invention provide a means of removing dyes from keratin fibers under relatively mild conditions. This dye removal is accomplished through the use of bleaching compositions containing hydrogen peroxide and bicarbonate salts.
  • the present invention is especially useful to people who have dyed their hair and wish to return their hair to its original color or for people who wish to have variegated hair coloring.
  • the coloring of keratin fibers is normally achieved by the use of chemical dyes.
  • dyes used to color keratin fibers. These dyes include, but are not limited to, semi-permanent dyes, direct dyes, oxidative dyes, and reactive dyes. Oxidative dyes are commonly used when permanently coloring human hair.
  • human hair can be taken as representative of the class of fibers known as keratin fibers.
  • the use of human hair as an example should not limit the scope of applications for the present invention as it is commonly known that animal fibers, such as wool and furs, are considered keratin fibers.
  • the coloring of hair with oxidative dyes in its simplest form is achieved by a process wherein small compounds known as dye intermediates are caused to react with one another in a process called coupling.
  • This coupling reaction requires initiation my an oxidizing agent such as hydrogen peroxide.
  • an oxidizing agent such as hydrogen peroxide.
  • bicarbonate salts in conjunction with oxidizing agents, such as hydrogen peroxide, will remove oxidative dye molecules not only from the surface of the dyed keratin fibers, but will also remove dye molecules deposited within the cortex of the fiber. Additionally, the higher the concentration of bicarbonate ions present in the bleaching composition, the faster the rate and the greater the degree of dye removal from the hair.
  • compositions useful in the present invention contain a bicarbonate salt or blend of bicarbonate salts yielding a bicarbonate concentration from about 2.0 x 10 2 mole percent to about 4.0 x 10 " ' mole percent of the final bleaching mixture.
  • bicarbonate concentrations here as mole percent.
  • Mole percent represents the number of moles of bicarbonate anion per 100 g of finished formulation. When formulating a product, these mole percent values can be converted to weight percent by simply multiplying the given mole percent by the molecular weight of the pure bicarbonate salt.
  • the actual weight percent of the individual bicarbonate salts used in any given bleaching composition is dependent on the molecular weight of the cation associated with the bicarbonate ion in said salt.
  • sodium bicarbonate has a molecular weight of 84.01. Of that total the molecular weight of the sodium cation is 22.99 and bicarbonate is 61.02.
  • Guanidine bicarbonate has a molecular weight of 120.09 of which the guanidine cation comprises 59.07 and the bicarbonate anion is 61.02.
  • bicarbonate salt is any agent or combination of agents capable of generating bicarbonate anion in solution.
  • compositions useful in the present invention preferably contain an amount of hydrogen peroxide, or peroxygen compound capable of generating hydrogen peroxide in solution, sufficient to yield an active oxygen content of from about 0.1 wt% to about 10.0 wt% and more preferably from about 2.5 wt% to about 7.0 wt%.
  • active oxygen is defined as the concentration of oxidant which can be readily determined by the standard assay procedures set forth by the Cosmetic, Toiletry, and Fragrance Association, Inc. (CTFA) Methods E29-1 and E30-1 issued in October, 1994.
  • CTFA Cosmetic, Toiletry, and Fragrance Association, Inc.
  • the hydrogen peroxide component of the present invention may also contain stabilizers, thickeners, and such ingredients which, when added to the peroxide solution, impart aesthetic properties without destabilizing hydrogen peroxide.
  • the pH of the compositions of the present invention should be maintained in the range where bicarbonate is the predominant species over carbonate or carbon dioxide.
  • This range is accepted to be the pH range of from about 7.0 to about 10.5. More preferably, a pH within the range of from about 7.5 to about 9.5 should be maintained.
  • compositions of the present invention may contain various penetration enhancing agents.
  • common penetration enhancing agents include but are not limited to urea and ammonia.
  • the benefit of certain penetration aides may be limited by their ability to convert the highly desirable bicarbonate to its ineffective carbonate form or to carbon dioxide.
  • ammonium hydroxide is routinely added to bleaching compositions of the current art to enhance the action of peroxide on natural melanin pigments.
  • the hydroxide ion of ammonium hydroxide readily converts the necessary bicarbonates to their ineffective carbonate form. Therefore, care should be exercised when using penetration enhancers so that an excess of bicarbonate anion is always present in the finished composition.
  • ingredients such as stabilizers for inhibiting the decomposition of peroxide, thickening agents and other ingredients which, when added, provide aesthetic qualities to the composition or to the treated hair may also be incorporated into the present invention provided that these materials do not convert the bicarbonate salts to their carbonate form or to carbon dioxide.
  • examples of such ingredients include, but are not limited to, conditioning agents, gelling agents, and moisture retention aides.
  • any soluble bicarbonate salt may be used in the present invention including, but not limited to, sodium bicarbonate, guanidine bicarbonate, ammonium bicarbonate, lithium bicarbonate, and potassium bicarbonate.
  • salts of known bicarbonate content are used in the compositions of the present invention. But the method of combining carbonate salts with an acidic material can be used to generate bicarbonate in situ with the same end result.
  • the bicarbonate salt comprises from about 0.1 to about 30 wt% of the bleaching composition. More preferably, the composition contains from about 2.0 to about 20 wt% of the bicarbonate salt. Additionally, the composition preferably contains from about 0.5 to about 30 wt% of a peroxygen compound (capable of giving an active oxygen titer of from 0.1 wt% to about 10.0 wt% using the CTFA Methods described above). More preferably, the bleaching composition contains from about 8.0 to about 20 wt% of the peroxygen compound.
  • weight percents for the bicarbonates are just general ranges and are dependent on the type of bicarbonate salt used. As stated earlier, the actual weight percent will depend on the amount of a particular bicarbonate needed to achieve the desired mole percents discussed above. Also, the actual amounts used will depend on the color of the dyed hair and the degree of dye removal desired.
  • the present invention may be used to enable an individual to obtain variegated hair colors.
  • a person who wants variegated hair must section the hair and apply a different coloring or bleaching solution to each section of the hair. This process is very time-consuming, expensive, and until now not subject to being reversed if dyes were used to impart multiple hues to the hair.
  • an individual would be able to initially dye their hair one color, and then selectively add a bicarbonate/peroxygen composition to different parts of their hair to remove the dye from those parts, thereby creating variegated hair in a process involving fewer steps than the processes currently used by hair-care professionals.
  • This process for obtaining variegated hair is especially useful for individuals who have chemically treated their hair before coloring it.
  • an individual chemically treats their hair such as relaxing or straightening it, the chemicals used tend to dull the hair.
  • hair dyes tend to add sheen to the hair, thereby countering the dulling effect.
  • the present invention allows an individual with curly hair to consecutively relax their hair, obtain a variegated hair color using dyes and the compositions of the present invention, and retain the added sheen imparted to the hair by the dye treatment.
  • a bicarbonate/peroxygen composition is supplied and either applied to only a portion of the fibers, to remove small areas of color, or to all of the fibers, to remove all of the dyed color.
  • the present invention therefore, has a wide utility in a variety of different areas, such as the production of keratin based textiles.
  • bicarbonate salts which can be employed in this manner include but are not limited to sodium bicarbonate, potassium bicarbonate, and guanidine bicarbonate.
  • ammonium bicarbonate and guanidine bicarbonate are the salts of choice, effective color removal from the dyed hair is achieved at concentrations of bicarbonate lower than those of potassium and sodium bicarbonates. It is, however, preferred that the total bicarbonate content of the bleaching composition remain within the range of the mole percents previously determined to provide the desired color removal.
  • Example 13 bicarbonates were added to a commercial hair-bleaching product using a packet of dry, powdered bicarbonate salt or a mixture of bicarbonate salts. This approach was chosen to illustrate the ability of bicarbonate salts to impart dye removal properties to commercial bleaching products and to show the effectiveness of systems more complex than simple aqueous solutions. As can be seen from the following discussion, the addition of bicarbonates to commercial hair bleaching compositions, which are normally effective only against natural hair pigments, converts these formulations to highly effective dye removers.
  • Bicarbonate salts were used to replace the High-Lift Booster (Part C) of a commercially-available, hair-bleaching product having the following composition:
  • Part A Developer (approximately 80 ml) Water, hydrogen peroxide, polyquaternium-37, mineral oil, PPG-1 trideceth-6, pentasodium pentetate, and phosphoric acid.
  • Part B Color Base (approximately 48 ml)
  • HEDTA sodium sulfite, sodium erythorbate, TEA-cocoyl hydrolyzed collagen, potassium cocoyl hydrolyzed collagen, p-phenylenediamine, 4-chlororesorcinol, m-aminophenol, and
  • the instructions for product use required that the Booster of Part C be dissolved in the Developer of Part A.
  • the Color Base of Part B is then added to the blend of booster and developer and shaken well prior to application to the hair. This same procedure was followed in experiments replacing the High-Lift Booster with bicarbonates. In all tests, the finished mixture was applied to tresses of dyed hair for a total of treatment time of 30 min. Samples of the product prepared according to manufacturers directions were evaluated as controls in this experiment.
  • Tresses of hair dyed a dark-black color (See Table 1 of Example 1) were exposed to the product prepared according to the manufacturers instructions (with high-lift booster) and to samples of the product in which the Booster had been replaced with 16.0 grams of sodium bicarbonate.
  • the treated tresses showed that noticeably more of the dyed color was removed from the tresses treated with the formulation containing bicarbonate than those treated with the product containing the persulfate booster.
  • the product containing the High-Lift Booster had very little effect on the color of the dyed hair.
  • the use of bicarbonate overcame several other disadvantages of the current product.
  • the persulfate booster could only be dissolved in the developer with undesirable, vigorous and extended shaking. Because of the shaking necessary to dissolve the booster, the product foamed profusely. This foaming interfered with the addition of the color base to the developer. Further, the conditioning agent in the developer precipitated when the persulfate booster was added. The mixture containing the persulfate booster also developed a strong irritating odor. The sample containing sodium bicarbonate did not suffer from any of these problems.
  • bicarbonates can be added to an existing hair- bleach composition containing hydrogen peroxide and ammonia in a manner similar to that currently employed with persulfate boosters.
  • the bicarbonate salts should be added in an amount sufficient to ensure that all of the bicarbonate is not converted to its carbonate form by the hydroxide present in the product.
  • the presence of residual bicarbonate anion in the final mixture is crucial to achieving adequate removal of dyes from the hair.
  • the bicarbonate salt or salts of the invention should be present in a large excess of the amount needed to react with all of the hydroxide present in the product.
  • bicarbonate salts which can be employed in this manner include but are not limited to sodium bicarbonate, potassium bicarbonate, ammonium bicarbonate, lithium bicarbonate, and guanidine bicarbonate.
  • ammonium bicarbonate and guanidine bicarbonate are the salts of choice, effective color removal from the dyed hair is achieved at concentrations of bicarbonate lower than those of potassium and sodium bicarbonates. It is, however, preferred that the total bicarbonate content of the bleaching composition remain within the range of the mole percents previously determined to provide the desired color removal.
  • Example 14 In this example, bicarbonate salts were generated in situ by reaction of a carbonate salt with an acid.
  • sodium carbonate was used to replace the bicarbonate in the compositions of Examples 1 through 13.
  • the carbonate based compositions failed to remove color from the dyed hair.
  • the degree of lift obtained was comparable to the control formula which contained only hydrogen peroxide and ammonia (i.e. little or no change in the color of the dyed tresses).
  • a proton donor succinic acid
  • the degree of dye removal obtained was identical to that observed with the sodium bicarbonate compositions of Example 1 through 13.
  • Any carbonate salt capable of conversion to bicarbonate by the action of a proton donor can be used in this embodiment of the present invention.
  • Any material capable of donating a proton to convert carbonate to bicarbonate can be used in this embodiment of the present invention.
  • Examples of other carbonate salts which can be employed in this manner include but are not limited to sodium carbonate, potassium carbonate, ammonium carbonate, lithium carbonate, and guanidine carbonate.
  • Examples of proton donors which can be employed in this manner include but are not limited to inorganic acids, organic acids, and organic compounds which can act as proton donors within the pH range set forth in earlier portions of this document. It is understood, however, that it is the bicarbonate anion content of the bleaching composition rather than the residual carbonate or carbon dioxide which governs the ability of the final oxidizing mixture to remove dyes from keratin fibers.

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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)
  • Chemical & Material Sciences (AREA)
  • Inorganic Chemistry (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Emergency Medicine (AREA)
  • Cosmetics (AREA)

Abstract

Cette invention a trait à une technique et aux compositions afférentes permettant de décolorer des fibres kératiniques dans des conditions peu agressives. Cette décoloration est le fait de compositions contenant des sels de bicarbonate associés à des agents oxydants, à du peroxyde d'azote notamment, capables d'enlever non seulement des molécules oxydantes de colorant de la surface des fibres kératiniques colorées, mais également des molécules de colorant déposées dans la couche corticale de la fibre. Cette invention intéresse tout particulièrement les personnes qui, ayant teint leurs cheveux, désirent revenir à leur couleur d'origine ou celles qui souhaitent avoir une chevelure bariolée.
EP99925931A 1998-05-29 1999-05-27 Compositions et techniques afferentes de decoloration de fibres keratiniques colorees de maniere permanente Withdrawn EP1082087A4 (fr)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US8716198P 1998-05-29 1998-05-29
US87161P 1998-05-29
US13078498P 1998-10-09 1998-10-09
US130784P 1998-10-09
PCT/US1999/011741 WO1999060993A1 (fr) 1998-05-29 1999-05-27 Compositions et techniques afferentes de decoloration de fibres keratiniques colorees de maniere permanente

Publications (2)

Publication Number Publication Date
EP1082087A1 true EP1082087A1 (fr) 2001-03-14
EP1082087A4 EP1082087A4 (fr) 2004-12-22

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EP99925931A Withdrawn EP1082087A4 (fr) 1998-05-29 1999-05-27 Compositions et techniques afferentes de decoloration de fibres keratiniques colorees de maniere permanente

Country Status (3)

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EP (1) EP1082087A4 (fr)
AU (1) AU4211999A (fr)
WO (1) WO1999060993A1 (fr)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2011105620A (ja) * 2009-11-13 2011-06-02 Hoyu Co Ltd 毛髪化粧料組成物及びその使用方法
US8506651B2 (en) 2011-12-30 2013-08-13 L'oreal S.A. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8343238B1 (en) 2011-12-30 2013-01-01 L'oreal Sa. Process for altering the appearance of hair using a composition containing dyes and non-hydroxide bases
US8556994B2 (en) 2011-12-30 2013-10-15 L'oreal Process for altering the appearance of hair using a composition containing direct dyes and non-hydroxide bases
US8591872B2 (en) 2011-12-30 2013-11-26 L'oreal Composition and process for reducing the curl and frizziness of hair
US10596100B2 (en) 2012-12-19 2020-03-24 L'oreal Cosmetic compositions containing an alkoxysilane and a silsesquioxane resin
US11241369B2 (en) 2017-11-30 2022-02-08 L'oreal Skin-brightening compositions and methods
US11045398B2 (en) 2017-12-27 2021-06-29 L'oreal Skin-brightening compositions and methods
US11299599B1 (en) 2019-05-07 2022-04-12 Bcd Global Ltd. Rapid chemical methods for recovery of materials from waste sources

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US4129415A (en) * 1976-10-15 1978-12-12 American Cyanamid Company Method for removing permanent dyes from hair and other keratinaceous materials
WO1996026313A1 (fr) * 1995-02-23 1996-08-29 Carefibres Oy Substance fibreuse et procede de fabrication

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US3552403A (en) * 1967-11-13 1971-01-05 Joseph T Sestito Hair-coloring method and apparatus therefor
DE2023838C3 (de) * 1970-05-15 1974-01-31 Deutsche Gold- Und Silber-Scheideanstalt Vormals Roessler, 6000 Frankfurt Verfahren zum Bleichen von natürlichen oder synthetischen Fasern
JPH0676304B2 (ja) * 1986-12-01 1994-09-28 サンスタ−株式会社 毛髪脱色剤
JPH01163298A (ja) * 1987-12-18 1989-06-27 Aiko Mizunoya 毛染洗浄剤
DE4026235A1 (de) * 1990-08-18 1992-02-20 Wella Ag Persulfathaltige zubereitung in form eines granulats, 2-komponenten-mittel und verfahren zum entfaerben und blondieren von haaren
DE19543989A1 (de) * 1995-11-25 1997-05-28 Wella Ag Blondiermittel für menschliche Haare
GB9526633D0 (en) * 1995-12-29 1996-02-28 Procter & Gamble Hair colouring compositions

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Publication number Priority date Publication date Assignee Title
US4129415A (en) * 1976-10-15 1978-12-12 American Cyanamid Company Method for removing permanent dyes from hair and other keratinaceous materials
WO1996026313A1 (fr) * 1995-02-23 1996-08-29 Carefibres Oy Substance fibreuse et procede de fabrication

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See also references of WO9960993A1 *

Also Published As

Publication number Publication date
AU4211999A (en) 1999-12-13
EP1082087A4 (fr) 2004-12-22
WO1999060993A1 (fr) 1999-12-02

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