[go: up one dir, main page]

MXPA00000072A - Hair styling composition - Google Patents

Hair styling composition

Info

Publication number
MXPA00000072A
MXPA00000072A MXPA/A/2000/000072A MXPA00000072A MXPA00000072A MX PA00000072 A MXPA00000072 A MX PA00000072A MX PA00000072 A MXPA00000072 A MX PA00000072A MX PA00000072 A MXPA00000072 A MX PA00000072A
Authority
MX
Mexico
Prior art keywords
hair
acid
carbon atoms
polymers
composition
Prior art date
Application number
MXPA/A/2000/000072A
Other languages
Spanish (es)
Inventor
Stephen Robert Schofield
Original Assignee
Procter & Gamble The Company
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 Procter & Gamble The Company filed Critical Procter & Gamble The Company
Publication of MXPA00000072A publication Critical patent/MXPA00000072A/en

Links

Abstract

A hair styling composition is provided which is particularly suitable for use in the form of a mousse. The composition comprises up to 10%by weight of an organic adhesive polymer and up to 5%by weight of an ethoxylated alcohol having an aliphatic chain length of up to 16 carbon atoms and a degree of ethoxylation of from 3 to 20 ethoxy groups per mole, and a solvent such as water. The composition provides a foam which is stable at rest but which readily breaks down under shear to form a creamy liquid which can easily be worked into the hair.

Description

COMPOSITION PAR ?, STYLE HAIR ECHNICAL FIELD The present invention relates to a composition for styling hair that provides a flexible film texture and good combing retention. In particular, the invention relates to a composition for styling hair in the form of a foam.
BACKGROUND OF THE INVENTION The desire to make the hair retain a particular shape is widely maintained. The most common methodology to achieve this is the application of a composition to moistened hair, or after washing with shampoo and / or conditioning, or to stylized and dry hair. These styling compositions provide temporary fixation benefits and can be removed with water or by shampooing. The materials used in the compositions to provide the fixing benefits have generally been resins and have been applied in the form of foams, gels, lotions or sprays. Additionally, these styling compositions are formulated for additional purposes, such as shampooing, conditioning, treatment, dyeing and combinations of P96-the same. A main desire of the consumer with respect to the performance of styling compositions has been the ability to retain the hair. Frequent good retention has been associated with strong and prolonged hair styling and / or fixation. However, it has also been observed that styling compositions having a retention capacity exceeding a certain magnitude can also give the hair a harsh feeling, making combing difficult, as well as being difficult to remove by shampooing. In addition, in recent years, some customers have expressed a desire to have hair styling products that allow the rearrangement of hair without compromising the capacity of hair retention. Since styling compositions with good retention capacity commonly provide a rigid film texture, it was difficult to provide a flexible film texture composition that would allow rearrangement of the hair. In this way, there is a desire to have hair styling compositions that have good retention without compromising the ability to rearrange the hair, can provide a soft and supple feeling to the hair, and can be easily removed.
P964 of the hair in the wash with shampoo. It is also desirable to have a composition for styling the hair in the form of a foam that provides foams having improved stability at rest but which undergoes rapid crushing to form creamy liquids under shear stress.
SUMMARY OF THE NONVENTION Thus, the present invention provides a composition for styling hair, comprising, by weight: (a) up to about 10% of at least one organic adhesive polymer; (b) up to about 5% of at least one surfactant comprising an ethoxylated alcohol having a chain length of up to about 16 carbon atoms and an ethoxylation degree of from about 3 to about 20 ethoxy groups per mole; and (c) a solvent. The composition for hair styling according to the invention can be in any form suitable for application to hair, such as for example foams, gels, lotions or sprays. However, it is preferred that the composition be in the form of a foam also comprising a propellant.
DETAILED DESCRIPTION The organic polymer (a) is present in the composition in an amount of up to about 10% by weight, preferably from about 1 to 3% by weight and more preferably from about 2 to 2.5% by weight. The polymer can be any polymer for conventional organic styling, which include: cationic, anionic, amphoteric and neutral polymers. Cationic polymers are preferred, anionic and amphoteric. The ethoxylated alcohol (b) is present in an amount of up to about 5% by weight, more preferably, from about 0.1% to about 1.0% by weight. The ethoxylated alcohol can be used as the sole surfactant or in conjunction with a co-surfactant. In accordance with the present invention, it has been found that improved foams are provided by incorporating a small amount of an ethoxylated alcohol into a styling composition, including a styling polymer. The styling polymer is also incorporated in a small amount with respect to conventional compositions for styling hair.
It is known that surfactants stabilize liquid walls or lamellae within foam structures. In accordance with the invention, it has been found that the use of ethoxylated alcohols have a specific chain length and a specific degree of ethoxylation leads to improved stability of the lamellae. In addition, under shear conditions, the foam quickly collapses to leave a creamy lime that can be quickly applied to the hair for styling. The chain length of the major alcohol and the degree of ethoxylation can be adjusted within the specified ranges to influence the ability of the surfactant to stabilize the lamellae under different shear conditions. The composition according to the invention is described in greater detail in the following. All percentages herein are by weight of the compositions, unless otherwise indicated. All proportions are proportions by weight unless otherwise stated. The total of the components, except for the propellant, is subsequently defined herein as a "concentrate". For non-aerosol products that do not contain propellant, the concentrate is equal to the complete composition. All percentages, proportions and levels of ingredients referred to herein are based on the actual amount of the ingredient, and do not include solvents, bulking agents, or other materials with which the ingredient can be combined as commercially available products, unless Indicate otherwise. Any adhesive polymer suitable for application to hair can be used as the adhesive polymer in the present invention. These include, but are not limited to, the following: homopolymers and copolymers (including block copolymers and random copolymers) and silicone-containing polymers. As used herein, copolymers refer to any polymers that contain two or more different types of monomers. Random copolymers are the most commonly used. The polymer can be an amphoteric polymer selected, for example, from the following polymers (1) to (5). (1) Dialistanylaminoalkyl methyl (acrylate) or diallerylaminoalkyl (meth) acrylamide) polymers containing at least units of the formula: P964 Rl (I) I I CH2 I cos ~ where R1 denotes a hydrogen atom or a methyl group, R2 denotes an alkylene group having 1 to 4 carbon atoms, and denotes O or -NH- and R3 and R4 independently denote hydrogen or alejuyl? to 4 carbon atoms, and a cationic derivative consisting of a cationic surfactant agent crue containing at least one hydrogen atom attached to one or more fatty chains and which is optionally quaternized, or consisting of a cationic polymer of the polyamine, polyaminopolyamide type , or poly- (quaternary ammonium), the amine or the ammonium groups form part of the polymer chain or are bound to it. These polymers usually have a molecular weight of 500 to 2,000,000. Amphoteric polymers containing ejue units corresponding to the above formula (I) are in general in the form of copolymers containing, in addition to the units of the above-mentioned form (I), at least units of the formula: Rl CID [C__2 ~ C_ I C0OR5 wherein R1 is as defined above and R5 represents an alkyl or alkenyl radical having from 4 to 24 carbon atoms or a cycloalkyl radical having from 4 to 24 carbon atoms. It is also possible to use terpolymers, tetrapolymers or pentapolymers containing, in addition to the units (I) and (II) defined above, units of the formula: (III) I [CH2-C] - COOR * wherein R6 preferably denotes an alkyl or alkenyl group having from 1 to 3 carbon atoms and R1 is as defined above. The units of the formula (I) are preferably present in an amount of 25 to 45% by weight, the units of the formula (II) are preferably present in an amount of 5 to 65% by weight, and the units of the formula (III) are preferably present in an amount of up to 50% by weight with respect to to the total weight of the polymer. A preferred polymer is the copolymer containing units of the formulas (I), (II), and (III) in which Y denotes an oxygen atom, R2 denotes the group -C.Hj-, R1, R3 and R4 denote methyl, R5 denotes an alkyl group having from 4 to 18 carbon atoms and R6 denotes an alkyl group having from 1 to 3 carbon atoms. The average molecular weight of this polymer is preferably from 70,000 to 90,000. This polymer is sold under the trademark "Yukaformer" or "Diaformer" supplied by Mitsubishi Chemical Corporation. (2) The polymers resulting from the copolymerization of a vinyl monomer having a carboxyl group, such as acrylic acid, methacrylic acid, maleic acid, or alpha-chloroacrylic acid, and a basic monomer ejue is a substituted vinyl compound since it contains at least one basic nitrogen atom, such as methacrylates and dialkylaminoalejuyl acrylates and dialejuylaminoal? ruyl methacrylamides and -acrylamides. (3) β-polymers contain units derived from i) at least one monomer selected from acrylamides or methacrylamides substituted on the nitrogen by an alkyl radical, ii) at least one acid comonomer containing one or more reactive carboxyl groups, and iii) ) at least one basic comonomer, such as esters, with substituents of primary, secondary and tertiary amines and quaternary ammonium substituents, of acrylic and methacrylic acids, and the product resulting from the quaternization of dimethylaminoethyl methacrylate with dimethyl or diethyl sulfate . The most preferred N-substituted acrylamides or methacrylamides are groups in which the alkyl radicals contain from about 2 to about 12 carbon atoms, especially N-ethylacrylamide, N-tert-butylacrylamide, N-tert-octylacrylamide, N -octylacrylamide, N-decylacrylamide and N-dodecyl acrylamide and also the corresponding methacrylamides. The acidic comonomers are chosen more particularly from among acrylic, methacrylic, crotonic, itaconic, maleic and fumaric acids and also the maleic monoesters of maleic acid or fumaric acid in which the alkyl has from 1 to 4 carbon atoms. The preferred basic comonomers are aminoethyl, butylaminoethyl, N, N'-dimethylaminoethyl and N-tert-butylaminoethyl methacrylates. (4) The crosslinked and zwitterionic polyaminoamides derived partially from polyaminoamides of the general formula: - [OC-R-CO-Z] (I) wherein R represents a divalent radical derived from a saturated dicarboxylic acid, from an aliphatic onocarboxylic or dicarboxylic acid with an ethylenic double bond, or from an ester of a lower alkanol having from 1 to 6 carbon atoms and from these acids or from a radical derived from the addition of any of the acids in a bis-primary or bis-secondary amine, and Z denotes a radical of a bis-primary or mono-or bis-secondary polyarylene-polyamine, and preferably represents : i) in proportions of 60 to 100 mol%, the radical [NH- (CH2) x-NH] - (II) wherein x is 2 and N is 2 or 3, or alternatively x is 3 and n is 2, this radical is derived from diethylenetriamine, triethylenetetramine, or dipropylenetriamine; ii) in proportions from 0 to about 40 mol%, the radical above (II) where x is 2 and n is 1 and is derived from ethylenediamine, or the radical P964 / \ -N KN \ -_ _ / piperazine derivative; and iii) in proportions of from 0 to about 20 mol%, the radical -NH- (CH2) 6-NH-, derived from hexamethylenediamine, these polyamides are crosslinked by the addition of a bifunctional crosslinking agent selected from epihalogenhydrins, diepoxides, dianhydrides and bis-unsaturated derivative, using from about 0.025 to about 0.35 mol of crosslinking agent per amine group of the polyaminoamide, and alkylated by the reaction by acrylic acid, chloroacetic acid, or an alkane-sultone or its salts . The saturated carboxylic acids are preferably chosen from acids having from 6 to 10 carbon atoms, such as adipic acid, 2,2,4- and 2,4,4-trimethyladipic acids, terephthalic acid and acids with an ethylenic double bond. , such as acrylic, methacrylic and itaconic acids. The alkane sulfones used in the alejuylation are preferably propane or butane-sultone and the salts of the alkylating agents are preferably the sodium or potassium salts. (5) Polymers containing units P96 zwitterionics derived from the formula: R2 R4 I I R1-I-C-] 3C ~ N + - (cH2) y-coo- R '_3 R _5 wherein R1 denotes a polymerizable unsaturated group, such as an acrylate, methacrylate, acrylamide or methacrylamide group, x and y independently represent an integer from 1 to 3, R2 and R3 independently represent hydrogen, methyl, ethyl or propyl and R4 and R5 independently represent a hydrogen atom or an alkyl radical such that the sum of the carbon atoms of R4 and R5 does not exceed 10. Highly preferred amphoteric polymers include material commercially available as octylacrylamine / acrylates / butylaminoethyl methacrylate copolymers with the trademarks : AMPHOMER, AMPHOMER LV71, and AMPHOMER LV47 supplied by National Starch & Chemicals, and methacryloyl ethylbetaine / acrylates copolymers with the tradenames of: YUKAFORMER SM, YUKAFORMER 301, YUKAFORMER 510, YUKAFORMER M-75, and YUKAFORMER R250S supplied by Mitsubishi Chemical Corporation. The anionic polymers useful in the present P964 invention are polymers containing units derived from a carboxylic, sulfonic or phosphoric acid and usually have a molecular weight of about 500 to about 5,000,000. These polymers are water-soluble polymers, it being possible for this solubility to be obtained by neutralization. The carboxylic acid groups can be provided by unsaturated monocarboxylic or dicarboxylic acids, such as those "corresponding to the formula: R1 (A) n-COOH \ / C-C / \ R2 R3 wherein n is 0 or an integer from 1 to about 10, A denotes a methylene group optionally linked to the carbon atom of the saturated group, or to the adjacent methylene group in the case where n is greater than 1, via a heteroatom, such as oxygen or sulfur, Rx denotes a hydrogen atom or a phenyl or benzyl group, R 2 denotes a hydrogen atom, a lower alkyl group, or a carboxyl group and R 3 denotes a hydrogen atom, a lower alkyl group, CH .COOH, or a phenyl or benzyl group. Preferred anionic polymers containing carboxylic acid groups are: P964 (1) Homopolymers or copolymers of acrylic or methacrylic acid or salts thereof, and in particular, the products sold under the name VERSICOL E or K by BASF and under the name DARVAN No. 7 by Van der Bilt; acrylic acid / acrylamide copolymers sold in the form of their sodium salt under the name RETEN 421, 423 or 425 by HERCULES; and sodium salts of polyhydroxycarboxylic acids, sold under the name HYDAGEN F by HENKEL. (2) Copolymers of acrylic or methacrylic acid with a monoethylene monomer, such as ethylene, styrene, a vinyl or allyl ester or ester of acrylic or methacrylic acid optionally inserted into a polyalkylene glycol, such as polyethylene glycol, and optionally crosslinked. Other such copolymers contain an N-alkylated and / or N-hydroxylated acrylamide unit optionally in their chain, such as those sold under the name QUADRAMER 5 by American Cyanamid. (3) Copolymers derived from crotonic acid, such as those containing in their chain units of vinyl acetate or propionate and, optionally, other monomers such as allyl or metalyl esters, a vinyl ether or a vinyl ester of a linear or branched carboxylic acid , saturated, with a hydrocarbon chain of at least 5 carbon atoms, in case these polymers are to be grafted and crosslinked, or else a P964 vinyl, allyl or metalyl ester of a carboxylic or cyclic acid. Included in this class are those with the trade names RESYN 28-2930, 28-2913, and 28-1310 sold by National Starch & Chemicals (4) Polymers derived from maleic, fumaric and itaconic acids, or anhydrides with vinyl esters, vinyl ethers, vinyl halides, phenyl vinyl derivatives, acrylic acid and their esters, such as those sold under the name GANTREZ A, SP, and ES by ISP. Other polymers included in this class are copolymers of maleic, cyclic and itaconic anhydride with an allyl or metalic ester optionally containing an acrylamido or methacrylamido group, or with an α-olefin, acrylic or methacrylic acid ester, acrylic or methacrylic acid or vinylpyrrolidone in its chain; the anhydride groups can be monoesterified or monoamidated. (5) Polyacrylamides containing carboxylate groups. The polymers comprising sulphonic groups include polymers containing vinylsulphonic, styrenesulphonic, lignosulfonic or naphthalenesulphonic units. These polymers are selected, in particular, from: i) Salts of polyvinylsulfonic acid having a molecular weight of 1,000 to 100,000, and also copolymers P964 with an unsaturated comonomer, such as acrylic or methacrylic acid or an ester thereof and also substituted or unsubstituted acrylamide or methacrylamide, vinyl esters, vinyl ethers and vinylpyrrolidone. ii) Salts of polystyrenesulfonic acid, such as sodium salt sold by National Starch _ Chemical sold under the name of Flexan 500 and 130. iii) Salts of alkali metals or alkaline earth metals of sulphonic acids derived from lignin and, more particularly, calcium lignosulfonates or sodium lignosulfonates, such as the product sold under the name Merasperse C-21 by American Can Co. and the products of 10 to 14 carbon atoms sold by Avebene. iv) Polymers containing salified alcjuju naphthalenesulfonic acid units, such as the sodium salt sold under the name Darvan No. 1 by Van der Bilt. The anionic polymers herein "including anionic monomers are preferably used in the at least partially neutralized form, in order to assist in the removal ability of the hairspray cosmetic compositions when shampooing the hair. In the compositions according to the present invention, the neutralization of a polymer can be achieved by the use of an inorganic base, preferably KOH. However, an organic base can also be used, preferably P964 AMP (amino-methy1-propane1) and the mixture of organic and inorganic base, to effect the desired level of neutralization in hair styling compositions according to the present invention. In total, it should be used with the base from about 50% to about 100%, preferably from about 70% to about 100%, most preferably from about 80% to about 100% of the acid monomers of each polymer used. Any conventionally used base, organic or inorganic, can be used for the neutralization of acidic polymers with the proviso that they are used as specified herein. The hydroxides of alkali, alkaline earth, and amino alcohols are suitable neutralizers for use in the present invention. Examples of suitable organic neutralizing agents that may be included in the compositions of the present invention include amines, especially amino alcohols such as 2-amino-2-methyl-1,3-propanediol (AMPD), 2-amine-2. -ethyl-l, 3-propanediol (AEPD), 2-amino-2-methyl-1-propanol (AMP), 2-amino-1-butanol (AB), monoethanolamine (MEA), diethanolamine (DEA), triethanolamine (TEA), monoisopropanolamine (MIPA), diisopropanolamine (DIPA), triisopropanolamine (TIPA), dimethyl stearamine P964 (DMS) and amino-methyl-propanol (AMP) and mixtures thereof. Preferred neutralizing agents for use in the hair styling compositions of the present invention are potassium and sodium hydroxides. Highly preferred anionic polymers include commercially available material such as vinyl acetate / crotonic acid / vinyl neodecanoate copolymers and vinyl acetate / crotonic acid copolymers under the tradenames RESYN 28-2930, RESYN 28-2913, and RESYN 28- 1310 supplied by National Starch & Chemicals, and copolymers of acrylates and acrylate / acrylamide copolymers under the tradenames LUVIMER 100P, ULTRAHOLD 8, and ULTRAHOLD STRONG supplied by BASF Corporation. Cationic polymers useful in the present invention include: (1) Vinylpyrrolidone / quaternized dialkylaminoalkyl methacrylate or acrylate copolymers, such as those sold under the tradename Gafejuat 734 and 755N by the Gaf Corp. (2) Cellulose-ether derivatives cgue contain quaternary ammonium groups. (3) Cationic polysaccharides. (4) Cationic polymers chosen from the group containing: P964 polymers containing units of the formula: -A-Z ^ A-Z2- (I) wherein A denotes a radical containing two amino groups, preferably a piperazinyl radical, and Z1 and Z2 independently denote a divalent radical which is a straight or branched chain alkylene radical containing up to about 7 carbon atoms in the main chain, substituted or unsubstituted with one or more hydroxyl groups and may also contain one or more hydrogen, nitrogen or sulfur atoms, and one to three heterocyclic and / or aromatic rings, the oxygen, nitrogen and sulfur atoms are generally present in the form of an ether or thioether, sulfoxide, sulfone, sulfonium, amine, alkylamine, alkenylamine, benzylamine, amine oxide, quaternary ammonium, amide, imide, alcohol, ester and / or urethane group; ii) polymers containing units of the formula: -A-Z * -A-Z '- (II) where A denotes a radical containing two amino group, P964 preferably a piperazinyl radical, and Z 'denotes the symbol Z3 and Z4, insofar as it denotes the symbol Z4 at least once; Z3 denotes a divalent radical which is a straight or branched chain straight or branched hydroxyalkylene radical having up to about 7 carbon atoms in the main chain, and Z4 is a divalent radical which is a straight or branched chain alkylene radical having up to about 7 carbon atoms in the main chain, unsubstituted or substituted with one or more hydroxyl radicals and interrupted by one or more nitrogen atoms, the nitrogen atom is replaced by an alkyl chain having from 1 to about 4 carbon atoms , preferably 4 carbon atoms, and is optionally interrupted by an oxygen atom and optionally contains one or more hydroxyl groups; and iii) The alkylation products with alkyl and benzyl halides of 1 to 6 carbon atoms, tosylates or alkyl mesylates and the oxidation products of the polymers of formulas (I) and (II) indicated above in i) and ii). (5) Polyamino-polyamines prepared by the polycondensation of an acid compound with a polyamide. The acid compound can be organic dicarboxylic acid, monocarboxylic acid and dicarboxylic acid containing double bond, esters of the aforementioned acids P964 above, preferably esters with lower alkanois having from 1 to 6 carbon atoms, and mixtures thereof. The polyamine is a bis-primary or mono- or bis-secondary polyalkylene-polyamine, wherein up to forty mole percent of this polyamide can be a bis-primary amine, preferably ethylene diamine, or a bis-secondary amine, preferably piperazine, and up to 20 mol% can be hexamethylenediamine. (6) The polyamino-polyamides mentioned above can be alkylated and / or crosslinked. The alkylation can be carried out with glycidol, ethylene oxide, propylene oxide or alkylamide. The crosslinking is carried out by means of a crosslinking agent such as: i) epihalogenhydrins, diepoxides, dianhydrides, unsaturated anhydrides and bis-saturated derivatives, in proportion of about 0.025 to about 0.35 mol of crosslinking agent per amine group of the polyamino -polyamide; ii) bis-halogenohydrins, bis-acetidinium compounds, bishalogen-acildiamines and bis- (haloalkyl halides); iii) oligomers obtained by reacting a compound selected from the group comprising bis-halohydrazines, bis-acetydinium compounds, bis- P964 halogenoacyl diamines, bis- (alkyl halides), epihalogenhydrins, diepoxides and bis-unsaturated derivatives, with another compound which is a difunctional compound which is reactive with the compound; and iv) the quaternization product of a compound selected from compounds ii) and oligomers iii) and containing one or more tertiary amino groups, which may be wholly or partly alkylated with an alkylating agent selected preferably from mesylates and tosylates, Methyl or ethyl bromides, iodides, sulfates and chlorides, benzyl chloride or bromide, ethylene oxide, propylene oxide and glycidol, the crosslinking is carried out by means of 0.025 to 0.35 mol, in particular from about 0.025 to about 0.2 mol and more particularly from about 0.025 to 0.1 mol, of the cross-linking agent per amine group of the polyamino-polyamide. (7) Polyamino-polyamide derivatives which result from the condensation of a polyalkylene oxide-polyamine with a polycarboxylic acid, followed by allegilation by bifunctional agents, such as the adipic acid / dialkylaminohydroxyalkyl dialkylenetriamine copolymers, in which the alcjuyl radical contains from 1 to 4 carbon atoms and preferably denotes ethyl, methyl or propyl. Useful polymers are acid copolymers P964 adipic / dimethylaminohydroxypropyl-diethylenetriamine sold under the name of Cartaretine F, F4 or F8 by SANDOZ. (8) The polymers obtained by reacting polyalkylenepolyamine containing two primary amine groups and at least one secondary amine group, with a dicarboxylic acid chosen from diglycolic acid and saturated aliphatic dicarboxylic acids having from about 3 to about 8 carbon atoms, molar ratio of the polyalkylene polyamine to the dicarboxylic acid which is from about 0.8: 1 to about 1.4: 1, and the resulting polyamine which is reacted with epichlorohydrin in a molar ratio of epichlorohydrin to the secondary amine groups of the polyamine from about 0.5: 1 to approximately 1.8: 1. Useful polymers are those sold under the name HERCOSETT 57 by Hercules Incorporated, and those sold under the name PD 170 or DELSETTE 101 by Hercules. (9) Cyclic polymers having in general a molecular weight of 20,000 to 3,000,000 such as homopolymers which contain, as the main constituent of the chain, units corresponding to the formula (III) or (III ') P964 < CH2) P (IIU \ (CH2 > t-R "C CR" -CH2 1) H2C CH2 \ / N + / \ R R '(CH2) p (I? I'I / \ \ / N in which p and t are 0 or 1, and p + t = 1, R "denotes hydrogen or methyl, R and R 'independently denote an alkyl having from 1 to 22 carbon atoms, a hydroxyalkyl in which the alkyl group preferably has 1 to 5 carbon atoms, or a lower amidoalkyl group, and R and R 'may denote together with the other nitrogen atom to which they are attached, heterocyclic groups such as piperidinyl or morpholinyl , and Y is bromide, chloride, acetate, borate, citrate, tartrate, bisulfate, bisulfite, sulfate or phosphate. Polymers containing units of formulas III and III 'may also contain units derived from acrylamide or diacetone acrylamide.
P964 Among the quaternary ammonium polymers of the type defined above, those which are preferred are the dimethyl dialkyl ammonium chloride homopolymer sold under the name MERQUAT 100 and having a molecular weight of less than 100,000, and the dimethyldialkyl ammonium chloride / acrylamide copolymer and has a molecular weight of more than 500,000 sold under the name of MERQUAT 550 by CALGON Corporation. (10) Poly- (quaternary ammonium) compounds of the formula Rl R3 wherein R1, R2, R3 and R4 are independently aliphatic, alicyclic or arylaliphatic radicals containing a maximum of 20 carbon atoms, or lower hydroxyaliphatic radicals, or alternatively, with the nitrogen atoms to which they are attached they form heterocyclic rings containing optionally a second hetero atom other than hydrogen, or alternatively R 1, R 2, R 3 and R 4 represent a group CH 2 CHR 3R 1 wherein R 1 J denotes hydrogen or lower alkyl and R 4 denotes SO, CN, CON (R , s) 2, COOR'5, COR'5, COOR 'J, or P964 CONHR'7D; R'5 denotes lower alkyl, R, d denotes hydrogen or lower alkyl, R'7 denotes alkylene and D denotes a quaternary ammonium group; A and B independently represent a polymethylene group containing from 2 to 20 carbon atoms, which may be linear or branched, saturated and unsaturated and may contain, inserted in the main chain one or more -CH2-Y-CH2- groups wherein Y denotes benzene, oxygen, sulfur, SO, S02, SS, NR'8, N * (R, 9), Xl, CHOH, NHCONH, CONR '8 or C00; X1"denoting an anion derived from mineral or organic acid, R'8 denoting hydrogen or lower alkyl and R'9 denotes lower alkyl or, alternatively, A and R1 and R3 form a piperazine ring with the two nitrogen atoms at which are joined If A denotes a hydroxyalkylene or alkylene radical, branched linear, saturated or unsaturated, B denotes a group: - (CH2) r-C0-D-0C- (CH2) n-; where n is selected so that the molecular weight is generally between 1,000 and 100,000, and D denotes: i) a glycol radical of the formulas -OZ-0, in which Z denotes a linear or branched hydrocarbon radical or a group corresponding to the formula: - [CH.-CH.-Ol ^ -CH.-CH, - or - [CH, -C (CH3) HO-]? CH2-C (CH.) H- where x and y denote a whole number of 1 to 4, which represents a defined and unique degree of polymerization, ii) a bis-secondary diamine radical, such as P964 a piperazine derivative; iii) a bis-primary diamine radical of the formula: -NHY-NH-, in which Y denotes a linear or branched hydrocarbon radical or the divalent radical - CH.-CH.-SS-CH.-CH.-; or iv) a ureylene group of the formula -N-H-CO-NH- (11) Homopolymers or copolymers derived from acrylic or methacrylic acid and containing at least one unit of: Rl Rl Rl I I I -CH2-C- (V) CH2-C- (V) -CH2-C- (V I I I c = o c «o C =« 0 I I f o o NH I I A A I I N R2-N + -R4- R2-N + -.- R4 / \ I R5 R6 _ X "3 X" where R1 is H or CH. , A is a linear or branched alkynyl group having 1 to 6 carbon atoms or a hydroxyalkyl group having 1 to 4 carbon atoms, R2, R3 and R independently denote an alkyl group having from 1 to 18 carbon atoms or a benzyl group, R5 and R6 denote H or alkyl having 1 to 6 carbon atoms and X denotes methosulfate or halide, such as chloride or bromide.
P961 The comonomer or comonomers that may be used typically correspond to the family comprising: acrylamide, methacrylamide, diacetone-acrylamide, acrylamide and methacrylamide substituted on the nitrogen by one or more lower alkyl, esters of acrylic and methacrylic acids, vinylpyrrolidone and esters vinyl Useful polymers are Quaternium 38, 37, 49 and 42 defined in CTFA, copolymers of acrylamide / beta-methacryloyloxyethyltrimethylammonium methosulphate sold under the names Teten 205, 210, 220 and 240 by Hercules, and the aminoethyl acrylate-phate copolymer / acrylate sold under the name Catrex by 'National Starch &; Chemicals, and cross-linked cationic graft polymers having a molecular weight of 10,000 to 1,000,000, and preferably 15,000 to 500,000, and resulting from the copolymerization of: at least one cosmetic monomer, dimethylaminoethyl methacrylate, polyethylene glycol and a polyunsaturated crosslinking, such as those mentioned in the CTFA dictionary under the name AMODIMETHICONE, as the product sold as a mixture with other ingredients under the name 929 of the DOW CORNING cationic emulsion. (12) Other cationic polymers that can be used are polyalkyleneamines, in particular polyethylene vanadines, polymers containing units of P9 £. vinylpyridine or vinylpyridinium units in the chain, condensates of polyamines and epichlorohydrin, poly- (quaternary ureilenes) and chitin derivatives. The silicone-containing adhesive polymers that can be used include any polymer containing one or more portions of silicone and one or more portions with adhesive carbon chain base, wherein, upon drying the solvent, the product is usually separated into a continuous phase and a discontinuous phase, wherein one of the phases can be any carbonaceous material or other carbohydrate material, and provide the adhesive properties of the polymer. Preferably, the silicone forms a discontinuous phase after drying and the carbon or carbohydrate portion forms the continuous phase. Alternatively, the silicone-containing polymers may be in the form of block copolymers wherein both portions form discontinuous phases. The preferred silicone-containing polymers are silicone-grafted vinyl basic structure polymers such as those set forth in EP 0 412 704, incorporated herein by reference, especially silicone-grafted polymers comprising acrylic acid / t-butyl acrylate base structures. Other adhesive polymers that can be used include, without limitation: elastomeric polymers P964 thermoplastics, such as those disclosed in PCT / US / 007387 (WO 95/01384), which are incorporated herein by reference. Highly preferred cationic polymers including commercially available material such as Polyquaternium 4 under the names CELQUAT HlOO and CELQUAT L200 supplied by National Starch Chemicals and Poliquaternium 11 sold under the name GAFQUAT 755N supplied by ISP. The surfactant component (b) of the composition according to the invention comprises essentially an ethoxylated alcohol having an aliphatic chain length, preferably alkyl, of up to about 22 carbon atoms and an ethoxylation degree of from about 3 to about 30. Ethoxy groups per mole, corresponding to the following structure: CH3- (CH,) a- (OCH, CH2) n-OH (I) wherein a has an average value of 1 to about 22, preferably and n has an average value of 3 to 30. The length of aliphatic chain, preferably alkyl, of the ethoxylated alcohol is preferably up to 16 carbon atoms, more preferably up to 14 carbon atoms and more preferably up to 12 carbon atoms. A C9-n ethoxylated alcohol is the most preferred.
P9ó The degree of ethoxylation of the ethoxylated alcohol is preferably about 4 to 20, more preferably about 5 to 16, most preferably about 6 to 12, and particularly preferably about 7 to 9 ethoxy groups per mole. The chain length ratio of aliphatic alcohol to degree of ethoxylation of the ethoxylated alcohol is preferably from about 7: 4 to 4: 7, more preferably from about 6: 4 to 5: 6, with particular preference of about 6: 4. at 1: 1 and most preferably at about 5: 4. Examples include: Pareth 8 C -_ ..; 'Pareth 8 Cll-13 and Pareth 9 C ,. . A particularly preferred ethoxylated alcohol is Pareth 8 C, u. The ethoxylated alcohol can be used alone or in conjunction with a surfactant. Examples of suitable co-surfactants include other nonionic surfactants that provide softeners for the foam, when the composition is in the form of a foam, such as polyoxyethylene, a polyoxypropylene, and mixtures thereof. Non-limiting examples of additional non-ionic surfactants for uLilizaise in the composition for the styling of the present invention are the following: P964 (1) Polyoxyethylene alkenyl ethers having the following general structure: CH, - (CHJ.-CH = CH (CHJ (OCH.CH.), -OH (ID where b has an average value of 1 to 10, c has an average value of 1 to 10, n has an average value of 2 to 200; (2) Alkyl or alkenyl or iso-alkyl or iso-alkenyl ethers of polyoxypropylene, or dimethylpolysiloxane having the following general structure: R'-C * -OCHÍ * CH_J. 'CHJJ _- (OCH._CH, 2 -OH (III) wherein R1 is selected from the group consisting of alkyl, alkenyl, isoalkylalkenyl, and dimethylpolysiloxane derivatives, x has an average value of 2 to 100; and has an average value of 2 to 100; (3) An ether derived from benzene or from long-chain alkyl and polyoxyethylene acid or having the following general structure: R-- (OCH.CH, ¡-OH (IV) where RQ is selected from the group consisting of P964 of castor oil triglyceride ricinolate, cholesterol, coconut oil triglyceride cocoate, alkylphenol, glyceryl laurate, glyceryl oleate, glyceryl cocoate, glyceryl isostearate, glyceryl stearate, hydrogenated castor oil glycerin ricinolate hydrogenated, hydrogenated lanolin, nonyl phenyl derivatives and dimethyl polysiloxane, and n has an average value of 2 to 200; (4) Polyoxyethylene alkyl or alekenyl ether having the following general structure: R3-C (0) - (OCH, CHjn-0-C (0) -R4 (V) wherein R3 and R4 are independently selected from the group consisting of alkyl, isoalkyl and alkenyl and n having an average value of from 2 to 200: (5) Long chain alkyl acid or iso-alkenyl fat, alkyl fat and polyoxypropylene has the following general structure; wherein R5 is selected from the group consisting of alkyl, isoalkyl and alkenyl, and n has an average value of from 2 to 200.
P964 The solvents used in the present invention are selected depending on variables such as the rest of the components, viscosity and desired foaming characteristics of the composition. The non-limiting examples and solvents useful in the present invention are: water, lower alcohols having from 1 to 6 carbon atoms such as ethanol and isopropanol, and polyhydric alcohols such as polyethylene glycol, hexylene glycol, glycerin and propanediol, and mixtures of the same. For foam and solvent compositions, it comprises at least about 80% water, more preferably at least about 90% water. The solvent is preferably comprised at a weight level from about 60% to about 99%, more preferably from about 80% to about 99%, and most preferably from about 85% to about 98% of the concentrate .
OPTIONAL COMPONENTS Other components may be included in the hair styling compositions of the present invention, depending on the needs of the product. The non-limiting examples of these optional components P964 include conditioning agents, preservatives, perfumes, ultraviolet and infrared light absorption and filtering agents, colorants, pH adjusters, additional non-ionic polymers, additional surfactants, dyes, vitamins, proteins, plant extracts and nutrients.
Conditioning Agents The conditioning agents may be comprised in the hair styling composition of the present invention. Suitable conditioning agents include fatty alcohols, fatty acids and hydrocarbons. Fatty alcohols useful herein are those having from about 10 to about 30 carbon atoms, preferably from about 12 to about 22 carbon atoms, and most preferably from about 16 to about 22 carbon atoms. These fatty alcohols may be straight or branched chain alcohols and may be saturated and unsaturated. Non-limiting examples of fatty alcohols include decyl alcohol, undecyl alcohol, dodecyl alcohol, myristyl alcohol, cetyl alcohol, stearyl alcohol, isostearyl alcohol, isocetyl alcohol, behenyl alcohol, P964 linalool, oleyl alcohol, cholesterol, cis-4-t-butylcyclohexanol, myric alcohol and mixtures thereof. Especially preferred fatty alcohols are those selected from the group consisting of cetyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol and mixtures thereof. The fatty acids useful herein are those having from about 10 to about 30 carbon atoms, preferably from about 12 to about 22 carbon atoms, and more preferably from about 16 to about 22 carbon atoms. These fatty acids may be straight or branched chain acids and may be saturated or unsaturated. They also include diacids, triazides and other multiple acids that satisfy the requirement of the carbon numbers herein. Salts of these fatty acids are also included herein. Non-limiting examples of fatty acids include lauric acid, palmitic acid, stearic acid, behenic acid, arachidonic acid, oleic acid, isostearic acid, sebacic acid and mixtures thereof. Especially preferred for use herein are the fatty acids selected from the group consisting of palmitic acid, stearic acid, and mixtures thereof. The hydrocarbons are useful herein as P964 conditioning agents. Useful hydrocarbons include straight chain, cyclic hydrocarbons and branched chain hydrocarbons which may be saturated and unsaturated. The hydrocarbons will preferably have from about 12 to about 40 carbon atoms, more preferably from about 12 to about 30 carbon atoms, and more preferably from about 12 to about 22 carbon atoms. Also encompassed herein are the polymeric hydrocarbons of alkenyl monomers, such as polymers of alkenyl monomers of 2 to 6 carbon atoms. These polymers can be straight or branched chain polymers. The straight chain polymers will typically be of relatively short length, with a total number of carbon atoms as described above in this paragraph. The branched chain polymers can have substantially larger chain lengths. The numerical average molecular weight of these materials can vary widely, but will typically be up to about 500, preferably from about 200 to about 400, and more preferably from about 300 to about 350. Also useful herein are the various grades of mineral oils. The oils P964 minerals are liquid mixtures of hydrocarbons that are obtained from petroleum. Specific examples of suitable hydrocarbon materials include paraffin oil, mineral oil, dodecane, isododecates, hexadecane, isohexadecane, eicosene, isoeicosene, tridecane, tetradecane, polybutene, polyisobutene and mixtures thereof. Isododecane, isohexadecane, and isoeicosene are commercially available as Permethyl 99A, Permethyl 101A, and Permethyl 1082, from Presperse, South Plainfield, NJ. A normal isobutene and butene polymer is commercially available as Indopol H-100 from Amoco Chemical. Preferred for use herein are the hydrocarbon conditioning agents selected from the group consisting of mineral oil, isododecane, isohexadecane, polybutene, polyisobutene, and mixtures thereof. When included, these two conditioning agents are comprised at a weight level from about 0.01% to about 2% of the concentrate.
Conservative The hair styling compositions of the present invention may additionally comprise a preservative. This preservative is preferably included at a weight level of up to about 5%, in more P9C4 preferred up to about 3% of the concentrate. Non-limiting examples of preservatives useful in the present invention are DMDM hydantoin (dimethylol-dimethylhydantoin), Katon CG (mixture of methylchloro-isothiazolinone and methyl isothiazolinone), imidazolidinyl urea, phenoxyethanol, EDTA and its salts, benzyl alcohol and Parabens, such as methyl paraben, propyl paraben, butyl paraben and LiquaPar oil (mixture of isobutylparaben, isopropyl paraben, and butyl paraben).
Other optional components The hair styling compositions of the present invention may additionally comprise a variety of optional components. These optional components include: thickeners and viscosity modifiers such as long chain fatty acid diethanolamides, sodium chloride and sodium sulfate, ultraviolet light absorbing agents such as ethyl salicylate, pH adjusting agents, such as citric acid, succinic acid , sodium hydroxide and triethanolamine, coloring agents, hair oxidizing agents, such as hydrogen peroxide, perborate salts, persulfate salts, hair reducing agents such as thioglycolates, perfumes, perfume solubilizing agents such as polyethylene glycol fatty acid esters , sequestering agents, agents P964 polymer plasticizers such as glycerin and propylene glycol and volatile and non-volatile low molecular weight silicone fluids. These optional ingredients are typically included in the weight level of up to about 20%, preferably -preferred to about 10% of the concentrate.
Compositions for Hair Styling The present invention encompasses a wide variety of compositions for hair styling, including: spray compositions, foams and hair setting tonics. In general, the compositions may flow, they will be low viscosity compositions that are preferably suitable for spray application. However, compositions of higher viscosity are also contemplated. The hair spray compositions of the present invention can be dispensed from containers that are aerosol dispensers or spray dispensers by pumping. These dispensers, i.e., containers, are well known to those of skill in the art and are commercially available from a variety of manufacturers, including: American National Can Corp. and Continental Can Corp. When the spray compositions for The hair P964 are to be dispensed from a pressurized aerosol container, a propellant consisting of one or more of the conventionally known aerosol propellants can be used to impel the compositions. A suitable propellant to be used may be, in general, any liquefiable gas, used conventionally for aerosol containers. Propellants suitable for use are the volatile hydrocarbon propellants which may include liquefied lower hydrocarbons of 3 to 4 carbon atoms, such as propane, butane and isobutane. Other suitable propellants are hydrofluorocarbons such as: 1,2-difluoroethane (Hydrofluorocarbon 152A) supplied as Dymel 152A by DuPont. Other examples of propellants are dimethyl ether, nitrogen, carbon dioxide, nitrous oxide and atmospheric gas. Hydrocarbons, particularly isobutane, used alone or mixed with other hydrocarbons, are preferred. The aerosol propellant can be mixed with the present compositions and the amount of propellant to be mixed is determined by normal factors well known in the aerosol field. Generally, for propellants that can liquefy, the propellant level is from about 10% to about 60% by weight of the P964 total composition, preferably from about 15% to about 50% by weight of the total composition. Alternatively, pressurized aerosol dispensers can be used where the propellant is separated from contact with the hair spray composition such as, for example, a two-compartment can of the type sold under the trademark SEPRO of American National Can Corp. Other suitable aerosol dispensers are those characterized in that the propellant is compressed air that can be filled inside the dispenser by means of a pump or equivalent device, before being used. These dispensers are described in U.S. Patents 4,077,441 and 4,850,577 and in U.S. Serial No. 07 / 839,648, Gosselin et al., Filed on February 21, 1992, The appropriate compressed air aerosol containers. to be used are also currently marketed by The Procter & Gamble Company under its trade name VIDAL SASSOON AIRSPRAY, sprays for hair. Spray dispensers can also be used by pump that are not aerosols, conventional, that is to say, atomizers. Other compositions for the styling of the P964 hair include tonics and lotions, which are normally dispensed in a conventional bottle or tube, and applied directly to the hair or dispensed first in the hand and then to the hair.
Method of Production The hair styling compositions of the present invention can be made using conventional blended formulation techniques. Preferably, a premix of the polymer and the solvent is first made. The other ingredients can then be added with mixing to provide a homogeneous mixture.
METHOD FOR USE The compositions of the present invention are used in conventional ways to provide the hair styling and preservation benefits of the present invention. These methods generally include the application of an effective amount of the product to dry, moisten lightly, or wet the hair before and / or after the hair is arranged in a desired style. The composition is then dried and allowed to dry. By "effective amount" is meant an amount sufficient to provide the benefits of P964 style and hair setting desired, considering the length and texture of the hair. In general, it will be applied to the hair, from approximately 0.5g to approximately 30g of the product, depending on the particular product formulation, the type of dispenser, the length of the hair and the type of hair style. The present invention is further illustrated with reference to the following Examples. Hair styling compositions are formulated as foams by conventional techniques known in the art. All the examples provided foams that were stable at rest for a long period of time but that, when subjected to shear stress, underwent rapid crushing to form creamy liquids that could be easily and effectively worked on the hair.
P964 n DOBANOL 91-8: - C9-11 Pareth 8 provided by Shell m DMDM hydantoin: - dimethylol dimethyl hydantoin í3i Fragrance Takasago 6397: - perfume supplied by Takasago The Examples showed that the relative proportions of the polymer and the ethoxylated alcohol can be adjusted to provide optimum foam properties. Specifically, the foams resulting from the compositions of the Examples, showed that increasing the polymer level from 2.0% (Example 1) to 2.25% (Example 2) and 2.5% (Example 3) and maintaining at the same time the same level of Ethoxylated alcohol, provides a higher viscosity construction and poorer performance speed. In addition, increasing the level of ethoxylated alcohol from 0.25% (Example 4) to 0.5% (Example 5) 0.75% (Example 6) and 1.0% (Example 7) while maintaining the same polymer level results in a characteristic of rubber and increased stiffness in the foam and the foam becomes harder to break under shear stress.
P964

Claims (2)

    CLAIMS: 1. A hair styling composition comprising, by weight: (a) up to 10% of at least one organic polymer; (b) up to 5% of at least one surfactant comprising an ethoxylated alcohol having an aliphatic chain length of up to 16 carbon atoms and a degree of ethoxylation of from 3 to 20 ethoxy groups per mole; and (c) a solvent. 2. A composition for hair styling according to claim 1, which is in the form of a foam also comprising a propellant. 3. A hair styling composition according to claim 1 or 2, wherein the surfactant (b) comprises from 0.1% to 1% by weight of the ethoxylated alcohol. 4. A composition for hair styling according to claim 1 to 3, wherein the surfactant comprises an ethoxylated alcohol C, ... having a degree of ethoxylation of 8 ethoxy groups per mole. 5. A composition for styling hair according to any of claims 1 to 4, wherein the polymer is selected from amphoteric adhesive organic polymers. 6. A composition for the styling of the
  1. P964 hair according to any of claims 1 to 5, comprising from 1% to 3% by weight of at least one polymer (a). 7. A composition for hair styling according to claim 6, comprising up to 5% by weight of at least one polymer (a). 8. A composition for hair styling according to claim 7, comprising from 2% to
  2. 2.5% by weight of at least one polymer (a). P96.
MXPA/A/2000/000072A 1997-06-30 2000-01-03 Hair styling composition MXPA00000072A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB9713862.2 1997-06-30

Publications (1)

Publication Number Publication Date
MXPA00000072A true MXPA00000072A (en) 2000-09-08

Family

ID=

Similar Documents

Publication Publication Date Title
US20020085988A1 (en) Hair styling composition
US4842849A (en) Composition intended for the treatment of keratin fibres, based on a cationic polymer and an anionic polymer containing vinylsulphonic groups
US4761273A (en) Composition in the form of an aerosol foam, based on a cationic polymer and an anionic polymer
AU745846B2 (en) Hairstyling composition comprising a polymer with particular characteristics and an ionic film forming polymer
US6585965B1 (en) Hair care compositions comprising polyalkylene glycol styling agents
US6589510B2 (en) Volume-imparting hair treatment product for strengthening the hair shaft
FR2737660A1 (en) COSMETIC COMPOSITION WITH FIXING POWER AND / OR CONDITIONER CONTAINING A PARTICULAR ACRYLIC COPOLYMER
KR19990082382A (en) Cosmetic aerosol fixing composition that provides a luster, and a preparation method thereof
EP0938284B1 (en) Hair styling composition
JP3095420B2 (en) Composition for the treatment of keratin fibers containing at least one anchoring polymer and at least one ceramide type compound and a method thereof
EP0796611B1 (en) Hair styling mousse
MXPA98002962A (en) Composition for the treatment of keratinic fibers, covering at least one fixed polymer and at least one compound of type ceramid and procedure
US7029661B1 (en) Cosmetic composition with a fixing and/or conditioning polymer containing a specific acrylic copolymer
FR3090342A1 (en) Cosmetic hair composition in the form of a nanoemulsion comprising a particular nonionic surfactant and a propellant
US7279153B2 (en) Hair treatment composition containing a combination of three different film-forming hair-fixing polymers
KR19980703786A (en) Nonionic Foaming Agent for Foaming Cosmetic Composition
CN105283223B (en) Cosmetic compositions comprising mineral waxes, fatty acids, mineral oils, surfactants, esters of fatty acids and/or fatty alcohols and fixed polymers
ES2243091T3 (en) WATERY PREPARATIONS FOR HAIR CARE.
GB2326889A (en) Hair styling composition
MXPA00000072A (en) Hair styling composition
KR20060050047A (en) Cosmetic compositions comprising linear sulfone polyesters and nonionic thickening polymers in non-fatty media, methods of using the compositions and uses thereof
MXPA00002720A (en) Non-aerosol mousse compositions
JP4203009B2 (en) Hair care composition
MXPA99004175A (en) Hair styling composition
WO2023275282A1 (en) Composition of single-phase appearance comprising a nonionic surfactant and an amphoteric surfactant