WO2013131752A2

WO2013131752A2 - Hair care composition

Info

Publication number: WO2013131752A2
Application number: PCT/EP2013/053433
Authority: WO
Inventors: Nicholas John Ainger; Stephen Norman Batchelor; Neil Stephen Burnham; Robert George Riley
Original assignee: Unilever Plc; Unilever N.V.; Conopco, Inc., D/B/A Unilever
Priority date: 2012-03-07
Filing date: 2013-02-21
Publication date: 2013-09-12
Also published as: WO2013131752A3; AR090262A1

Abstract

A kit for colouring hair, comprising: (i) an aqueous shampoo composition comprising a) a cleansing surfactant; b) a polymer formed from at least 20 wt% of the total weight of polymer of carboxylic acid containing monomers; c) a polyphenol; in which the weight ratio of polymer b) to polyphenol c) is from 12:1 to 1:12; and ii) a second aqueous second composition, which comprises a cationic surfactant and at least 0.01 wt% of a metal ion selected from an Fe(II), Fe(III) or mixtures thereof in the form of a salt and/or complex.

Description

Hair Care Composition

The present invention relates to kits and methods for colouring hair. Background

Polyphenol compound mordanted with metal ions have been known to dye human hair for many years. Two part colouring systems are described in EP0327345 (Beecham) and

WO2010/135237 (Advance Cosmetic Technologies).

JP 04/164,017 (Lion) discloses a system for colouring hair consisting of shampoo containing a surfactant and gallic acid, tannic acid, salicylic acid, derivatives thereof, pyrogallol, catechol or haematin as a first agent. This is used in conjunction with a second agent containing a polyvalent metal salt and a cationic surfactant.

Such systems can stain textiles, such as cotton towels, used to dry wet hair. The present invention relates to a way of mitigating the staining of fabrics.

Description of the Invention

Accordingly the present invention relates to a kit for colouring hair, comprising: (i) an aqueous shampoo composition comprising

a) a cleansing surfactant;

b) a polymer formed from at least 20 wt% of the total weight of polymer of carboxylic acid containing monomers;

c) a polyphenol; in which the weight ratio of polymer b) to polyphenol c) is from 12:1 to 1 :12; and

ii) a second aqueous second composition, which comprises a cationic

surfactant and at least 0.01 wt% of a metal ion selected from an Fe(ll), Fe(lll) or mixtures thereof in the form of a salt and/or complex.

The invention further relates to a method of colouring hair comprising the steps of applying to the hair sequentially compositions the kit described above. Shampoo Formulation

Shampoo compositions of the invention are generally aqueous, i.e. they have water or an aqueous solution or a lyotropic liquid crystalline phase as their major component. Suitably, the composition will comprise from 50% to 98%, preferably from 60% to 90% water by weight based on the total weight of the composition.

Cleansing Surfactant

Shampoo compositions according to the invention will generally comprise one or more cleansing surfactants which are cosmetically acceptable and suitable for topical application to the hair. The cleansing surfactant is preferably an anionic cleansing surfactant.

Examples of suitable anionic cleansing surfactants are the alkyl sulphates, alkyl ether sulphates, alkaryl sulphonates, alkanoyl isethionates, alkyl succinates, alkyl sulphosuccinates, alkyl ether sulphosuccinates, N-alkyl sarcosinates, alkyl phosphates, alkyl ether phosphates, and alkyl ether carboxylic acids and salts thereof, especially sodium, magnesium, ammonium and mono-, di- and

triethanolamine salts. The alkyl and acyl groups generally contain from 8 to 18, preferably from 10 to 16 carbon atoms and may be unsaturated. The alkyl ether sulphates, alkyl ether sulphosuccinates, alkyl ether phosphates and alkyl ether carboxylic acids and salts thereof may contain from 1 to 20 ethylene oxide or propylene oxide units per molecule. Typical anionic cleansing surfactants for use in shampoo compositions of the invention include sodium oleyl succinate, ammonium lauryl sulphosuccinate, sodium lauryl sulphate, sodium lauryl ether sulphate, sodium lauryl ether sulphosuccinate, ammonium lauryl sulphate, ammonium lauryl ether sulphate, sodium

dodecylbenzene sulphonate, triethanolamine dodecylbenzene sulphonate, sodium cocoyi isethionate, sodium lauryl isethionate, lauryl ether carboxylic acid and sodium N-lauryl sarcosinate.

Preferred anionic cleansing surfactants are sodium lauryl sulphate, sodium lauryl ether sulphate(n)EO, (where n is from 1 to 3), sodium lauryl ether

sulphosuccinate(n)EO, (where n is from 1 to 3), ammonium lauryl sulphate, ammonium lauryl ether sulphate(n)EO, (where n is from 1 to 3), sodium cocoyi isethionate and lauryl ether carboxylic acid (n) EO (where n is from 10 to 20).

Mixtures of any of the foregoing anionic cleansing surfactants may also be suitable.

The total amount of anionic cleansing surfactant in shampoo compositions of the invention generally ranges from 0.5% to 45%, preferably from 1 .5% to 35%, more preferably from 5% to 20% by total weight anionic cleansing surfactant based on the total weight of the composition.

Co-surfactant

The composition can include co-surfactants, to help impart aesthetic, physical or cleansing properties to the composition. An example of a co-surfactant is a nonionic surfactant, which can be included in an amount ranging from 0.5% to 8%, preferably from 2% to 5% by weight based on the total weight of the composition. For example, representative nonionic surfactants that can be included in shampoo compositions of the invention include condensation products of aliphatic (Cs - C-is) primary or secondary linear or branched chain alcohols or phenols with alkylene oxides, usually ethylene oxide and generally having from 6 to 30 ethylene oxide groups.

Other representative nonionic surfactants include mono- or di-alkyl alkanolamides. Examples include coco mono- or di-ethanolamide and coco mono- isopropanolamide. Further nonionic surfactants which can be included in shampoo compositions of the invention are the alkyl polyglycosides (APGs). Typically, APG is one which comprises an alkyl group connected (optionally via a bridging group) to a block of one or more glycosyl groups. Preferred APGs are defined by the following formula: RO - (G)n wherein R is a branched or straight chain alkyl group which may be saturated or unsaturated and G is a saccharide group. R may represent a mean alkyl chain length of from about C₅ to about C2o-

Preferably R represents a mean alkyl chain length of from about Cs to about C12. Most preferably the value of R lies between about 9.5 and about 10.5. G may be selected from C₅ or C6 monosaccharide residues, and is preferably a glucoside. G may be selected from the group comprising glucose, xylose, lactose, fructose, mannose and derivatives thereof. Preferably G is glucose. The degree of polymerisation, n, may have a value of from about 1 to about 10 or more. Preferably, the value of n lies from about 1.1 to about 2. Most preferably the value of n lies from about 1 .3 to about 1.5. Suitable alkyl polyglycosides for use in the invention are commercially available and include for example those materials identified as: Oramix NS10 ex Seppic; Plantaren 1200 and Plantaren 2000 ex Henkel.

Other sugar-derived nonionic surfactants which can be included in compositions of the invention include the C-IO-C-IS N-alkyl ( -Ce) polyhydroxy fatty acid amides, such as the C-12-C-18 N-methyl glucamides, as described for example in WO 92 06154 and US 5 194 639, and the N-alkoxy polyhydroxy fatty acid amides, such as C-IO-C-IS N- (3-methoxypropyl) glucamide. A preferred example of a co-surfactant is an amphoteric or zwitterionic surfactant, which can be included in an amount ranging from 0.5% to about 8%, preferably from 1 % to 4% by weight based on the total weight of the composition.

Examples of amphoteric or zwitterionic surfactants include alkyl amine oxides, alkyl betaines, alkyl amidopropyl betaines, alkyl sulphobetaines (sultaines), alkyl glycinates, alkyl carboxyglycinates, alkyl amphoacetates, alkyl amphopropionates, alkylamphoglycinates, alkyl amidopropyl hydroxysultaines, acyl taurates and acyl glutamates, wherein the alkyl and acyl groups have from 8 to 19 carbon atoms. Typical amphoteric and zwitterionic surfactants for use in shampoos of the invention include lauryl amine oxide, cocodimethyl sulphopropyl betaine, lauryl betaine, cocamidopropyl betaine and sodium cocoamphoacetate.

A particularly preferred amphoteric or zwitterionic surfactant is cocoamidopropyl betaine. Mixtures of any of the foregoing amphoteric or zwitterionic surfactants may also be suitable. Preferred mixtures are those of cocoamidopropyl betaine with further amphoteric or zwitterionic surfactants as described above. A preferred further amphoteric or zwitterionic surfactant is sodium cocoamphoacetate.

The total amount of surfactant (including any co-surfactant, and/or any emulsifier) in a shampoo composition of the invention is generally from 1 % to 50%, preferably from 2% to 40%, more preferably from 10% to 25% by total weight surfactant based on the total weight of the composition.

Polyphenol

The shampoo composition of the kit comprises a polyphenol. The polyphenol of the invention comprises at least one benzene ring substituted with a first OH group and a second OH or OCH₃ group, preferably OH. Preferably the first OH is ortho to the second OH group.

Polyphenols may be found in the classes of phenolic acid, Anthocyanin,

Anthocyanidin, flavanols, flavanones and gallates. For example flavan-3-ols, flavan-4-ols, flavan-3,4-ols. Gallic Acid, flavanols and flavanones are preferred.

A preferred polyphenol contains a benzene ring substituted in the:

1 position by an X group, wherein X is a carbon containing organic group, preferably selected from an ester group, COOH, chromenes and 3,4 dihydro- chromenes. 3 position by a H, OH or OCH₃ group, preferably an OH group.

4 position by an OH group. 5 position by an OH or OCH₃ group, preferably an OH group.

Most preferably the 2 and 6 positions are substituted by H. Preferably the polyphenol is a ortho-dihydroxybenzene derivative.

Preferably the polyphenol has a molecular weight of less than 1 ,000, more preferably less than 500.

Polyphenols may be suitably found in the wood and bark of trees and in the fruit, seeds and nuts of plants. For example the leaves of Camilla senesis; the wood of Haematoxylum campechianum; the bark of Quercus velutina; the fruit of Vitis vinifer; the fruit of Olea europaea; the roots of Curcuma demoestica; the trunk and bark of Quercus velutina and Quercus lusitanica; the trunk and bark of trees of the genus Pseudotsuga; the trunk and bark of Acacia catechu.

The polyphenol of the invention is preferably selected from gallic acid, methyl gallate, ethyl gallate, propyl gallate or mixtures thereof. Most preferably propyl gallate

Methyl gallate, ethyl gallate, propyl gallate are obtainable by esterification of gallic acid. Preferably the gallic acid is extracted from a natural source, preferably from hydrolysable tannins, preferably extracted from tara plants or gallnuts. Preferably, the polyphenols do not contain any active oxidase enzymes and have been heat treated to destroy any enzyme activity.

The polyphenol is preferably selected from methyl gallate, ethyl gallate and propyl gallate.

The polyphenol containing composition is preferably an aqueous polyphenol solution. The polyphenol composition preferably comprises from 0.05 wt% to 10.0 wt% of the total composition, more preferably from 0.1 wt% to 5.0 wt %, most preferably 0.2 wt% to 3.0 wt% of polyphenol. The polyphenol solution preferably has a pH at 20 °C of from 2 to 8 measured using a calibrated pH meter more preferably from preferably 3 to 7, most preferably from 0.5 to 6.5. To avoid oxidation of the polyphenols by air it is preferred that the composition is stored in an airtight container, preferably a bottle closed with an air tight cap.

The aqueous polyphenol solution contains water, preferably as the dominant ingredient. Auxiliary ingredients may be present for example to increase the viscosity, perfume and help solubilise the polyphenol. Solubilising ingredients include organic solvents and surfactants.

Preferably, the water used to formulate all compositions has a French hardness of from 0 to 36 degrees, more preferably 0 to 24 degrees, most preferably from 0 to 2 degrees.

Preferably, the water used to formulate all compositions contains less than 1 ppm of chlorine based bleaching agents such as chlorine dioxide or hypochlorite. Most preferably less than 50ppb.

Polycarboylic acid

The polymers of the invention comprise a polymer formed from at least 20 wt% of the total weight of polymer of carboxylic acid containing monomeric units, more preferably 50 wt%, most preferably 90 wt%, preferably the carboxylic acid containing monomeric unit is acrylic acid, thus the shampoo composition of the invention preferably comprise polymers comprising polyacrylic acids.

Such polymers are preferably polyacrylic acids per se, cross-linked polymers of acrylic acid, copolymers of acrylic acid with a hydrophobic monomer, copolymers of carboxylic acid-containing monomers and acrylic esters, cross-linked copolymers of acrylic acid and acrylate esters.

The weight average molecular weight of the polymer is preferably greater than 10,000, more preferably greater than 100,000, most preferably greater than 1 ,000,000.

The polymer preferably contains a mixture of acrylic acid and a crosslinker, preferably allyl sucrose or allyl pentaerythritol. A crosslinker in the context of the present invention is a compound containing 2 or more preferably 3 to 6 polymerisable double bonds, preferably acrylate groups. Preferably the mol ratio of acrylic acid to crosslinker is 850: 150 to 999:1 , more preferably 98:2 to 99:1 .

AlkyI methyacrylate are optionally present, preferably, methyl methacrylate, ethyl methacrylate, propyl methacrylate and butyl methacrylate.

The polymerisation is preferably accomplished via free radical polymerisation.

Preferably the polymer is water miscible and at 0.5 wt% in demineralised water has a zero shear viscosity of greater thanl 0,000 Pa.s (at shear stress of 1 Pa).

Polyacrylic acid is available commercially as Carbopol 420, Carbopol 488 or Carbopol 493. Polymers of acrylic acid cross-linked with a polyfunctional agent may also be used; they are available commercially as Carbopol 910, Carbopol 934, Carbopol 941 and Carbopol 980. An example of a suitable copolymer of a carboxylic acid containing monomer and acrylic acid esters is Carbopol 1342. All Carbopol (trademark) materials are available from Lubrizol.

Suitable cross-linked polymers of acrylic acid and acrylate esters are Pemulen TR1 or Pemulen TR2. The weight ratio of polymer comprising acrylic acid b) to polyphenol c) is from 12:1 to 1 :12, preferably from 3:2 to 1 :6, most preferably from 1 :1 to 1 :7.

Preferably the level of polycarboxylic acid polymer, preferably polyacrylic acid polymer, in the shampoo is from 0.05 to 2 wt% of the total shampoo composition, more preferably from 0.1 wt% to 1 wt%, most 0.2 to 0.6 wt%.

Cationic Polymers Cationic polymers are preferred ingredients in a shampoo composition of the invention for enhancing conditioning performance and to mitigate staining of fabrics.

Suitable cationic polymers may be homopolymers which are cationically substituted or may be formed from two or more types of monomers. The weight average (M_w) molecular weight of the polymers will generally be between 100,000 and 2 million daltons. The polymers will have cationic nitrogen containing groups such as quaternary ammonium or protonated amino groups, or a mixture thereof. If the molecular weight of the polymer is too low, then the conditioning effect is poor. If too high, then there may be problems of high extensional viscosity leading to stringiness of the composition when it is poured.

The cationic nitrogen-containing group will generally be present as a substituent on a fraction of the total monomer units of the cationic polymer. Thus when the polymer is not a homopolymer it can contain spacer non-cationic monomer units. Such polymers are described in the CTFA Cosmetic Ingredient Directory, 3rd edition. The ratio of the cationic to non-cationic monomer units is selected to give polymers having a cationic charge density in the required range, which is generally from 0.2 to 3.0 meq/gm. The cationic charge density of the polymer is suitably determined via the Kjeldahl method as described in the US Pharmacopoeia under chemical tests for nitrogen determination.

Suitable cationic polymers include, for example, copolymers of vinyl monomers having cationic amine or quaternary ammonium functionalities with water soluble spacer monomers such as (meth)acrylamide, alkyi and dialkyi (meth)acrylamides, alkyi (meth)acrylate, vinyl caprolactone and vinyl pyrrolidine. The alkyi and dialkyi substituted monomers preferably have C1 -C7 alkyi groups, more preferably C1 -3 alkyi groups. Other suitable spacers include vinyl esters, vinyl alcohol, maleic anhydride, propylene glycol and ethylene glycol.

The cationic amines can be primary, secondary or tertiary amines, depending upon the particular species and the pH of the composition. In general secondary and tertiary amines, especially tertiary, are preferred.

Amine substituted vinyl monomers and amines can be polymerized in the amine form and then converted to ammonium by quaternization.

The cationic polymers can comprise mixtures of monomer units derived from amine- and/or quaternary ammonium-substituted monomer and/or compatible spacer monomers.

Suitable cationic polymers include, for example: - cationic diallyl quaternary ammonium-containing polymers including, for example, dimethyldiallylammonium chloride homopolymer and copolymers of acrylamide and dimethyldiallylammonium chloride, referred to in the industry (CTFA) as Polyquaternium 6 and Polyquaternium 7, respectively; - mineral acid salts of amino-alkyl esters of homo-and co-polymers of unsaturated carboxylic acids having from 3 to 5 carbon atoms, (as described in U.S. Patent 4,009,256); - cationic polyacrylamides (as described in W095/2231 1 ).

Other cationic polymers that can be used include cationic polysaccharide polymers, such as cationic cellulose derivatives, cationic starch derivatives, and cationic guar gum derivatives. Cationic polysaccharides are particularly preferred as they mitigate the staining of fabrics.

Cationic polysaccharide polymers suitable for use in compositions of the invention include monomers of the formula: A-0-[R-N⁺(R )(R²)(R³)X^"], wherein: A is an anhydroglucose residual group, such as a starch or cellulose anhydroglucose residual. R is an alkylene, oxyalkylene, polyoxyalkylene, or hydroxyalkylene group, or combination thereof. R , R² and R³ independently represent alkyl, aryl, alkylaryl, arylalkyl, alkoxyalkyl, or alkoxyaryl groups, each group containing up to about 18 carbon atoms. The total number of carbon atoms for each cationic moiety (i.e., the sum of carbon atoms in R , R² and R³) is preferably about 20 or less, and X is an anionic counterion. Another type of cationic cellulose includes the polymeric quaternary ammonium salts of hydroxyethyl cellulose reacted with lauryl dimethyl ammonium-substituted epoxide, referred to in the industry (CTFA) as Polyquaternium 24. These materials are available from the Amerchol Corporation, for instance under the tradename Polymer LM-200. Other suitable cationic polysaccharide polymers include quaternary nitrogen- containing cellulose ethers (e.g. as described in U.S. Patent 3,962,418), and copolymers of etherified cellulose and starch (e.g. as described in U.S. Patent 3,958,581 ).

A particularly suitable type of cationic polysaccharide polymer that can be used is a cationic guar gum derivative, such as guar hydroxypropyltrimethylammonium chloride (commercially available from Rhodia in their JAGUAR trademark series). Examples of such materials are JAGUAR C13S, JAGUAR C14, JAGUAR C15, JAGUAR C17 and JAGUAR C16 Jaguar CHT and JAGUAR C162.

Mixtures of any of the above cationic polymers may be used.

Cationic polymer will generally be present in a shampoo composition of the invention at levels of from 0.01 % to 5%, preferably from 0.05 % to 1 %, more preferably from 0.08 % to 0.5% by total weight of cationic polymer based on the total weight of the composition.

Suspending Agent

Shampoo compositions of the invention may comprise suspending agents.

Ethylene glycol distearate and polyethylene glycol 3 distearate are preferred long chain acyl derivatives, since these impart pearlescence to the composition. , heteropolysaccharide gums and crystalline long chain acyl derivatives. The long chain acyl derivative is desirably selected from ethylene glycol stearate, alkanolamides of fatty acids having from 16 to 22 carbon atoms and mixtures thereof. A suitable heteropolysaccharide gum is xanthan gum, for example that available as Kelzan mu. Mixtures of any of the above suspending agents may be used. Suspending agent will generally be present in a shampoo composition of the invention at levels of from 0.1 % to 10%, preferably from 0.5% to 6%, more preferably from 0.9% to 4% by total weight of suspending agent based on the total weight of the composition.

Further Ingredients

Optionally, a shampoo composition of the invention may contain further ingredients as described below to enhance performance and/or consumer acceptability.

Product Form

Compositions of the invention are typically "rinse-off compositions to be applied to the hair and then rinsed away.

Conditioner Composition

One part of the kit comprises conditioner for the treatment of hair (typically after shampooing) and subsequent rinsing.

Such conditioner compositions will typically comprise one or more conditioning surfactants which are cosmetically acceptable and suitable for topical application to the hair.

Suitable conditioning surfactants include those selected from cationic surfactants, used singly or in admixture. Preferably, the cationic surfactants have the formula N⁺R R²R³R⁴ wherein R , R², R³ and R⁴ are independently (Ci to C₃o) alkyl or benzyl. Preferably, one, two or three of R , R², R³ and R⁴ are independently (C₄ to C₃o) alkyl and the other R , R², R³ and R⁴ group or groups are (C-i-Ce) alkyl or benzyl. More preferably, one or two of R , R², R³ and R⁴ are independently (C6 to C₃₀) alkyl and the other R , R², R³ and R⁴ groups are (CrC₆) alkyl or benzyl groups. Optionally, the alkyl groups may comprise one or more ester (-OCO- or - COO-) and/or ether (-0-) linkages within the alkyl chain. Alkyl groups may optionally be substituted with one or more hydroxyl groups. Alkyl groups may be straight chain or branched and, for alkyl groups having 3 or more carbon atoms, cyclic. The alkyl groups may be saturated or may contain one or more carbon- carbon double bonds (eg, oleyl). Alkyl groups are optionally ethoxylated on the alkyl chain with one or more ethyleneoxy groups.

Suitable cationic surfactants for use in conditioner compositions according to the invention include cetyltrimethylammonium chloride, behenyltrimethylammonium chloride, cetylpyridinium chloride, tetramethylammonium chloride,

tetraethylammonium chloride, octyltrimethylammonium chloride,

dodecyltrimethylammonium chloride, hexadecyltrimethylammonium chloride, octyldimethylbenzylammonium chloride, decyldimethylbenzylammonium chloride, stearyldimethylbenzylammonium chloride, didodecyldimethylammonium chloride, dioctadecyldimethylammonium chloride, tallowtrimethylammonium chloride, dihydrogenated tallow dimethyl ammonium chloride (eg, Arquad 2HT/75 from Akzo Nobel), cocotrimethylammonium chloride, PEG-2-oleammonium chloride and the corresponding hydroxides thereof. Further suitable cationic surfactants include those materials having the CTFA designations Quaternium-5, Quaternium-31 and Quaternium-18. Mixtures of any of the foregoing materials may also be suitable. A particularly useful cationic surfactant for use in conditioners according to the invention is cetyltrimethylammonium chloride, available commercially, for example as GENAMIN CTAC, ex Hoechst Celanese. Another particularly useful cationic surfactant for use in conditioners according to the invention is

behenyltrimethylammonium chloride, available commercially, for example as GENAMIN KDMP, ex Clariant. Another example of a class of suitable cationic surfactants for use in the invention, either alone or together with one or more other cationic surfactants, is a

combination of (i) and (ii) below:

(i) an amidoamine corresponding to the general formula (I):

in which R is a hydrocarbyl chain having 10 or more carbon atoms,

R² and R³ are independently selected from hydrocarbyl chains of from 1 to 10 carbon atoms, and

m is an integer from 1 to about 10; and (ii) an acid.

As used herein, the term hydrocarbyl chain means an alkyl or alkenyl chain.

Preferred amidoamine compounds are those corresponding to formula (I) in which

R is a hydrocarbyl residue having from about 1 1 to about 24 carbon atoms, R² and R³ are each independently hydrocarbyl residues, preferably alkyl groups, having from 1 to about 4 carbon atoms, and m is an integer from 1 to about 4.

Preferably, R² and R³ are methyl or ethyl groups.

Preferably, m is 2 or 3, i.e. an ethylene or propylene group.

Preferred amidoamines useful herein include stearamido-propyldimethylamine, stearamidopropyldiethylamine, stearamidoethyldiethylamine, stearamidoethyldimethylamine, palmitamidopropyldimethylamine,

palmitamidopropyl-diethylamine, palmitamidoethyldiethylamine,

palmitamidoethyldimethylamine, behenamidopropyldimethyl-amine,

behenamidopropyldiethylmine, behenamidoethyldiethyl-amine,

behenamidoethyldimethylamine, arachidamidopropyl-dimethylamine,

arachidamidopropyldiethylamine, arachid-amidoethyldiethylamine,

arachidamidoethyldimethylamine, and mixtures thereof.

Particularly preferred amidoamines useful herein are

stearamidopropyldimethylamine, stearamidoethyldiethylamine, and mixtures thereof.

Commercially available amidoamines useful herein include:

stearamidopropyldimethylamine with tradenames LEXAMINE S-13 available from Inolex (Philadelphia Pennsylvania, USA) and AMIDOAMINE MSP available from Nikko (Tokyo, Japan), stearamidoethyldiethylamine with a tradename

AM IDOAMINE S available from Nikko, behenamidopropyldimethylamine with a tradename INCROMINE BB available from Croda (North Humberside, England), and various amidoamines with tradenames SCHERCODINE series available from Scher (Clifton New Jersey, USA).

A protonating acid may be present. Acid may be any organic or mineral acid which is capable of protonating the amidoamine in the conditioner composition. Suitable acids useful herein include hydrochloric acid, acetic acid, tartaric acid, fumaric acid, lactic acid, malic acid, succinic acid, and mixtures thereof.

Preferably, the acid is selected from the group consisting of acetic acid, tartaric acid, hydrochloric acid, fumaric acid, lactic acid and mixtures thereof.

The primary role of the acid is to protonate the amidoamine in the hair treatment composition thus forming a tertiary amine salt (TAS) in situ in the hair treatment composition. The TAS in effect is a non-permanent quaternary ammonium or pseudo-quaternary ammonium cationic surfactant. Suitably, the acid is included in a sufficient amount to protonate more than 95 mole% (293 K) of the

amidoamine present.

In conditioners of the invention, the level of cationic surfactant will generally range from 0.01 % to 10%, more preferably 0.05% to 7.5%, most preferably 0.1 % to 5% by weight of the composition. Conditioners of the invention will typically also incorporate a fatty alcohol. The combined use of fatty alcohols and cationic surfactants in conditioning compositions is believed to be especially advantageous, because this leads to the formation of a lamellar phase, in which the cationic surfactant is dispersed. Representative fatty alcohols comprise from 8 to 22 carbon atoms, more preferably 16 to 22. Fatty alcohols are typically compounds containing straight chain alkyl groups. Examples of suitable fatty alcohols include cetyl alcohol, stearyl alcohol and mixtures thereof. The use of these materials is also advantageous in that they contribute to the overall conditioning properties of compositions of the invention.

The level of fatty alcohol in conditioners of the invention will generally range from 0.01 % to 10%, preferably from 0.1 % to 8%, more preferably from 0.2% to 7%, most preferably from 0.3% to 6% by weight of the composition. The weight ratio of cationic surfactant to fatty alcohol is suitably from 1 :1 to 1 :10, preferably from 1 :1 .5 to 1 :8, optimally from 1 :2 to 1 :5. If the weight ratio of cationic surfactant to fatty alcohol is too high, this can lead to eye irritancy from the composition. If it is too low, it can make the hair feel squeaky for some consumers. Metal Salt and/or Complex

Conditioner Compositions of the invention comprise a metal ion selected from an Fe(ll), Fe(l ll) or mixtures thereof in the form of a salt and/or complex. Metal ion containing compositions of the invention comprise 0.01 wt% of the total composition of a metal ion, preferably from 0.01 wt% to 10 wt%, more preferably from 0.1 wt% to 5 wt% of the total composition, more preferably from 0.2 to 3 wt%

The level of metal ion in the formulation may be determined by quantitative elemental analysis.

For the avoidance of doubt, if the formulation contains 2 wt% of the complex

With molecular weight of 446.14, then it will contain 55.84/446.14*2 = 0.25 wt% of Fe(ll) (2 decimal places).

The metal ion is preferably selected from Fe(ll) and Fe(lll).

The metal ion is preferably present as a complex with a ligand. The ligand is preferably organic in nature.

In the context of this invention a ligand is a molecule that contains more than one group, preferably 2 to 4 groups, most preferably 2 groups that co-ordinate with the metal ion. Groups for co-ordinating with the metal ion are COO^", OH, ketones, esters, primary amines, secondary amines and tertiary amines, more preferably COO^", tertiary amines and OH, most preferably COO^" and OH. Polyphenols are not permitted as multidentate ligands. The ligand-metal complex may be preformed before addition to the shampoo for example Iron (II) Gluconate, iron (II) Glutamate. The ligand metal complex may be formed in the composition by the addition of an iron salt and the ligand, for example FeC and sodium lactate. Preferably, the mole ratio of iron ion to ligand is from 1 :1 to 1 :4, more preferably from 1 : 1 .5 to 1 :2.5.

Preferably, the metal ion is in the form of a complex that is soluble in aqueous solution at the pH of the formulation. Most preferably the metal ion in the form of a salt and/or complex has a solubility in demineralised water at the pH of the formulation of greater than 0.1 g/L.

The ability of a ligand to complex with a metal ion, Mⁿ⁺, may be defined by its pMⁿ value, wherein

and the ligand concentration is 10^~5 mol/L and the total metal ion concentration is 10^~6 mol/L and [Mⁿ⁺]_free \s the molar concentration of uncomplexed metal ions. Preferably the ligand used has a lower pMⁿ⁺, than gallic acid. Preferably the pMⁿ⁺ are greater than 8 more preferably greater than 10. pMⁿ⁺ values are most preferably measured at pH=4 in de-mineralised water, with the chloride salt of the metal ion, most preferably ferric chloride. Polyamino carboxylic acids are preferably present at weight % levels of less than 1/30th of the main ligand, preferably they are absent from the conditioner. A polyamino carboxylic acid is a compound containing two or more amines

connected through carbon atoms to two or more carboxylic acid groups.

2,2',2",2"'-(Ethane-1 ,2-diyldinitrilo)tetraacetic acid is a polyamino carboxylic acid. Diethylene triamine pentaacetic acid is a polyamino carboxylic acid. Ethylenediamine-/V,/V'-disuccinic acid is a polyamino carboxylic acid. Most preferably the ligands are selected from gluconate, tartrate, ascorbate, citrate and lactate. Particularly preferred are gluconate, lactate or ascorbate. Particularly preferred are iron (II) gluconate, iron (I II) gluconate and iron (II) lactate, most preferably iron (II) gluconate and/or iron (III) gluconate.

Product form

To avoid oxidation of the metal by air it is preferred that the composition is stored in an air tight container such as a bottle closed with an air tight cap.

Further Conditioning Agents

Compositions of the invention; shampoos or conditioners; may comprise further conditioning agents to optimise wet and dry conditioning benefits.

The compositions of the invention can contain, emulsified droplets of a silicone conditioning agent, for enhancing conditioning performance. Silicone conditioning agents may be present in the shampoo or conditioner.

Suitable silicones include polydiorganosiloxanes, in particular

polydimethylsiloxanes which have the CTFA designation dimethicone. Also suitable for use compositions of the invention (particularly shampoos and conditioners) are polydimethyl siloxanes having hydroxyl end groups, which have the CTFA designation dimethiconol. Also suitable for use in compositions of the invention are silicone gums having a slight degree of cross-linking, as are described for example in WO 96/31 188.

The viscosity of the emulsified silicone itself (not the emulsion or the final hair conditioning composition) is typically at least 10,000 est at 25 °C the viscosity of the silicone itself is preferably at least 60,000 est, most preferably at least 500,000 est, ideally at least 1 ,000,000 est. Preferably the viscosity does not exceed 10⁹ est for ease of formulation. Emulsified silicones for use in the shampoo compositions of the invention will typically have an average silicone droplet size in the composition of less than 30 μΐη, preferably less than 20 μΐη, more preferably less than 10 μΐη, ideally from 0.01 μΐη to 1 μΐη. Silicone emulsions having an average silicone droplet size of≤ 0.15 μΐη are generally termed microemulsions.

Emulsified silicones for use in the conditioner compositions of the invention will typically have an size in the composition of less than 30 μΐη, preferably less than 20 μΐη, more preferably less than 15 μΐη. Preferably, the average silicone droplet is greater than 0.5 μΐη, more preferably greater than 1 μΐη, ideally from 2 μΐη to 8 μΐη.

Silicone particle size may be measured by means of a laser light scattering technique, for example using a 2600D Particle Sizer from Malvern Instruments. Examples of suitable pre-formed emulsions include Xiameter MEM 1785 and microemulsion DC2-1865 available from Dow Corning. These are emulsions /microemulsions of dimethiconol. Cross-linked silicone gums are also available in a pre-emulsified form, which is advantageous for ease of formulation A further preferred class of silicones for inclusion in shampoos and conditioners of the invention are amino functional silicones. By "amino functional silicone" is meant a silicone containing at least one primary, secondary or tertiary amine group, or a quaternary ammonium group. Examples of suitable amino functional silicones include: polysiloxanes having the CTFA designation "amodimethicone". Specific examples of amino functional silicones suitable for use in the invention are the aminosilicone oils DC2-8220, DC2-8166 and DC2-8566 (all ex Dow Corning). Suitable quaternary silicone polymers are described in EP-A-0 530 974. A preferred quaternary silicone polymer is K3474, ex Goldschmidt.

Also suitable are emulsions of amino functional silicone oils with non ionic and/or cationic surfactant.

Pre-formed emulsions of amino functional silicone are also available from suppliers of silicone oils such as Dow Corning and General Electric. Specific examples include DC939 Cationic Emulsion and the non-ionic emulsions DC2- 7224, DC2-8467, DC2-8177 and DC2-8154 (all ex Dow Corning).

With some shampoos it is preferred to use a combination of amino and non amino functional silicones

The total amount of silicone is preferably from 0.01 wt% to 10 wt% of the total composition more preferably from 0.1 wt% to 5 wt%, most preferably 0.5 wt% to 3 wt% is a suitable level, especially for a shampoo composition.

Other Optional Ingredients A composition of the invention may contain other ingredients for enhancing performance and/or consumer acceptability. Such ingredients include fragrance, dyes and pigments, pH adjusting agents, pearlescers or opacifiers, viscosity modifiers, preservatives, and natural hair nutrients such as botanicals, fruit extracts, sugar derivatives and amino acids. Method of use

The method of colouring hair comprising the steps of applying to hair sequentially (i) a shampoo composition as described above followed by

(ii) a conditioning composition as described above.

Preferably, the compositions of the invention are applied to wet hair, necessitating the step of wetting the hair before application of the compositions of the invention. It is highly preferred if the hair is rinsed after application of both compositions of the invention.

Further conditioning and/or styling products may be applied as part of the colouring process.

The level of each composition applied to the head of hair is preferably from 5g to 100g.

Preferably, each composition remains on the hair for 5 to 600 seconds, more preferably 10 to 300 seconds.

Preferably, the water used to wet and rinse the hair has a French hardness of from 0 to 36 degrees, more preferably 0 to 24 degrees, most preferably from 0 to 2 degrees.

Preferably, the water used to wet and rinse the hair contains less than 1 ppm of chlorine based bleaching agents such as chlorine dioxide or hypochlorite. Most preferably less than 50ppb The invention will now be illustrated by the following non-limiting examples. Examples of the invention are illustrated by a number comparative examples are illustrated by a letter. Examples

Example 1 Fabric staining

Shampoo's of the following composition (wt%) were made:

The surfactant used was Sodium lauryl ether sulphate (1 EO) and

cocoamidopropyl betaine in the ratio 15:2. The structurant used was carbopol 980 (ex Lubrizol).

The cationic polysaccharide polymer was guar hydroxypropyltrimethylammonium chloride (Jaguar C14 ex Rhodia). An iron containing conditioner formulation was also made of the following composition. Ingredient Weight%

Behentrimonium Chloride 1 .13

Stearamidopropyldimethylamine 0.38

Cetearyi Alcohol 4.00

Lactic Acid 0.10

Preservative 0.09

Iron (II) gluconate 4.00

Water To 100

0.7g of the shampoo was rubbed in to dry white woven cotton cloth and left for 30 minutes. 0.7g of the conditioner was then rubbed into the same area of the cloth and left for 30 minutes. The cloth was then rinsed in a bath of cold demineralised water for 30 minutes, in which the water was changed every 10 minutes. The cloths were dried and the colour measured using a reflectometer (CIE L*a*b* values) and the colour change expressed as the · E value before and after treatment. The results are shown below:

It should be noted that shampoo compositions comprising cationic

polysacchararide polymer and structurant stain fabric less than compositions omitting the cationic polysacchararide polymer. Both compositions stain fabric less than the compartative composition without structurant or cationic

polysaccharadide polymer. Example 2: hair colouration

0.7g of the shampoo was applied to a wet Chinese white hair truss weighing 0.7g. The product was left on the hair for 30 minutes, rinsed under a running tap, then 0.7g conditioner applied, left for 30 minutes, rinsed and dried. The colour of the hair was measured before and after treatment using a reflectometer and the colour change expressed as the · E value before and after treatment. The results are shown below.

Thus it is demonstrated that compositions according to the invention red staining of fabric without greatly reducing the colouring of hair.

Example 3

Shampoo

Timiron MP2000 Mica ί 0.15

Sodium Hydroxide I Sodium hydroxide To pH

Silicone DC 5-7051 HS I Dimethiconol, TEA- j Dodecylbenzenesulfonate

Jaguar BFG14 j Guar Hydroxypropyltrimonium Chloride j 0.2

Propyl Gallate j Propyl Gallate

Parfume ! Perfume 1 0.9

Water ! water I to 100

Conditioner

Ingredient Weight%

Behentrimonium Chloride 1 .13

Stearamidopropyldimethylamine 0.38

Cetearyl Alcohol 4.00

Lactic Acid 0.10

Preservative 0.09

Iron (II) gluconate 4.00

Water To 100

Claims

A kit for colouring hair, comprising:

(i) an aqueous shampoo composition comprising

a) a cleansing surfactant;

c) a polyphenol;

in which the weight ratio of polymer b) to polyphenol c) is from 12:1 to 1 :12; and

ii) a second aqueous second composition, which comprises a cationic surfactant and at least 0.01 wt% of a metal ion selected from an Fe(ll), Fe(lll) or mixtures thereof in the form of a salt and/or complex.

A kit according to claim 1 in which the polymer b) comprises polymeric acrylic acid.

A kit according to claim 1 or claim 2 in which the weight ratio of polymer b) to polyphenol c) is from 1 :1 to 1 :7.

A kit according to any preceding claim in which the cleansing surfactant comprises an anionic cleansing surfactant and is present at a level from 1 .5 wt% to 35 wt% of the total shampoo composition.

A kit according to any preceding claim in which the cleansing surfactant further comprises an amphoteric or zwitterionic surfactant.

6. A kit according to any preceding claim in which the level of polyphenol is from 0.1 wt% to 5.0 wt% of the total shampoo composition.

7. A kit according to any preceding claim in which the level of polyphenol is from 0.2 wt% to 3 wt% of the total shampoo composition.

8. A kit according to any preceding claim in which the polyphenol is selected from gallic acid, methyl gallate, ethyl gallate, propyl gallate or mixtures thereof.

9. A kit according to claim 8 in which the polyphenol is propyl gallate. 10. A kit according to any preceding claim in which the level of polymer

containing carboxylic acid b) in the shampoo composition is from 0.1 wt% to 1 wt% of the total composition.

1 1 . A kit according to any preceding claim in which the shampoo composition further comprises a cationic polysaccharide polymer

12. A kit as according to any preceding claim in which the metal ion complex comprises a ligand of gluconate, lactate or ascorbate. 13. A kit according to any preceding claim in which the metal ion is present as iron (I I) gluconate and/or iron (III) gluconate.

14. A kit according to any preceding claim in which the level of metal ion is from 0.01 wt% to 5 wt% of the conditioner composition.

15. A method of colouring hair comprising the steps of applying to the hair sequentially compositions of the kit described in the claims above.

16. A method according to claim 15 which further comprises the step of rinsing the hair between application of the compositions.