WO2013091999A2 - Agent cosmétique pour la mise en forme temporaire de fibres kératiniques - Google Patents

Agent cosmétique pour la mise en forme temporaire de fibres kératiniques Download PDF

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Publication number
WO2013091999A2
WO2013091999A2 PCT/EP2012/072343 EP2012072343W WO2013091999A2 WO 2013091999 A2 WO2013091999 A2 WO 2013091999A2 EP 2012072343 W EP2012072343 W EP 2012072343W WO 2013091999 A2 WO2013091999 A2 WO 2013091999A2
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formula
group
acid
cosmetic composition
composition according
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PCT/EP2012/072343
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German (de)
English (en)
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WO2013091999A3 (fr
Inventor
Burkhard Müller
Ulrike Heinsohn
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Henkel Ag & Co. Kgaa
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Publication of WO2013091999A2 publication Critical patent/WO2013091999A2/fr
Publication of WO2013091999A3 publication Critical patent/WO2013091999A3/fr

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    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44—Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/46—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur
    • A61K8/466—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing sulfur containing sulfonic acid derivatives; Salts
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/92—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922—Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00—Preparations for care of the hair
    • A61Q5/06—Preparations for styling the hair, e.g. by temporary shaping or colouring

Definitions

  • the present invention relates to the temporary transformation of keratinous fibers, in particular human hair.
  • Healthy hair and a pleasing-looking hairstyle is now generally considered an indispensable part of a well-groomed appearance.
  • the human feels dull hair or thin hair as an aesthetic blemish. If the hair is exposed to environmental influences, e.g. Exposed to UV radiation, mechanical stress or free radicals, the hair structure can be adversely affected. This affects the external appearance.
  • hair splitting e.g. The hair tips are visibly degenerated in their hair structure and make the hair look sick and unhealthy.
  • Cosmetic agents which protect the hair or change the properties of the hair in such a way that the appearance of the hair approximates the desired ideal of beauty serve as aids.
  • Corresponding means for temporary shaping usually contain fixing polymers as the shaping component.
  • Preparations containing a dissolved or dispersed polymer can be applied to the hair by means of propellant gases or by a pumping mechanism.
  • hair gels and hair waxes are generally not applied directly to the hair, but distributed by means of a comb or hands in the hair.
  • foams can be easily and evenly distributed on the hair.
  • the foams must fulfill a special requirement profile so that the application can be carried out optimally and the effect of the polymers on the hair can develop accordingly.
  • the foams must form quickly, remain stable for a short time and break on the hair, so that no permanent foam hood is formed. The foam must not strain the hair, otherwise the imprinted hairstyle hangs out and is therefore lost.
  • the most important property of a composition for the temporary deformation of keratinic fibers is to give the treated fibers in the produced form the strongest possible hold. If the keratin fibers are human hair, it is also referred to as a strong hairstyle or the high degree of retention of the styling agent.
  • the hairstyle hold is essentially determined by the type and amount of setting polymer used, but also an influence of the other components of the styling can be given by means of and the type of application.
  • styling agents In addition to a high degree of hold, styling agents must meet a whole range of other requirements. Particular mention should be made of moisture resistance, low tack and a balanced conditioning effect.
  • the polymers when applied to hair, the polymers give a polymer film which, on the one hand, gives the hairstyle strong hold but, on the other hand, is sufficiently flexible not to break under stress. If the polymer film is too brittle, it results in the formation of so-called Filmpiaken, that is residues that detach during the movement of the hair and give the impression that the user of the corresponding styling agent would dandruff.
  • care agents are additionally added to the cosmetic products which do not or only very slightly dissolve in water.
  • Object of the present invention was therefore to provide a cosmetic agent with propellant available, which is characterized by a high degree of hold. Furthermore, the agent should simultaneously have a flexible hold and show a high care performance.
  • the formation of Filmpiaken - in particular the formation of corresponding residues in the application, the brushing and drying of the keratin-containing fiber - should be avoided. If the means are designed as foam, the foam should form quickly, only when applied to the hair will begin to break significantly. Furthermore, a foam should be provided which does not stress the hair.
  • a first subject of the invention is therefore a cosmetic agent for the cosmetic treatment of keratinic fibers, in particular human hair, containing
  • R is a linear or branched, saturated or unsaturated hydrocarbon radical
  • R 2 is a hydrogen atom, a (C 1 to C 4 ) -alkyl group or a (C 2 to C 4 ) -
  • O M independently represents a hydrogen atom or one equivalent of a monovalent or polyvalent cation
  • M independently of one another denotes a hydrogen atom or one equivalent of a mono- or polyvalent cation
  • n 1 or 2
  • R is a (C 8 to C 2 2) -alkyl group, a mono- or polyunsaturated (C 8 to C 2 2) -alkenyl group or a group R 2 - (O-CH 2 CH 2 ) m- *,
  • R 2 is a (C 8 to C 2 2) -alkyl group or a mono- or polyunsaturated (C 8 to C 2 2) -alkenyl group , and
  • keratinic fibers are understood to mean furs, wool, feathers and, in particular, human hair.
  • Examples of (C 1 to C 4 ) -alkyl groups according to the invention are methyl, ethyl, n-propyl, isopropyl, n-butyl, sec-butyl, isobutyl, tert-butyl.
  • Examples of (C 2 to C 4 ) hydroxyalkyl groups according to the invention are 2-hydroxyethyl, 3-hydroxypropyl, 2-hydroxypropyl and 4-hydroxybutyl.
  • a hydrocarbon radical according to the invention consists exclusively of carbon and hydrogen.
  • the radicals R of the formula (I) preferably stand for a (C 9 to C 23 ) -alkyl group or a (C 9 to C 23 ) -alkenyl group having up to four unsaturated double bonds, more preferably independently of one another, selected from the group consisting of List formed from nonyl, undecyl, tridecyl, pentadecyl, heptadecyl, nonadecyl, henicosanyl, 15-methylhexadecyl, heptadec-8-enyl, heptadeca-8,1-dienyl, nonadeca-4,7, 10, 13- tetraenyl and heptadeca-8, 11, 14-trienyl.
  • the radical R 2 according to formula (I) preferably represents a radical selected from the group consisting of hydrogen atom, methyl, ethyl, isopropyl, n-propyl and 2-hydroxyethyl. Particularly preferably, said radical R 2 is a hydrogen atom or a methyl group. In the event that R 3 is a hydrogen atom, R 2 is preferably a methyl group.
  • R 2 is preferably a hydrogen
  • R 3 according to formula (I) particularly preferably represents a hydrogen atom.
  • the radical M is a hydrogen atom.
  • M is one equivalent of a monovalent or polyvalent cation.
  • the monovalent or polyvalent cation M z + each having a charge number z of one or higher serves merely to neutralize the charge of the carboxylate fragment -COO ⁇ -) of the formula (I), which is present for reasons of electroneutrality.
  • the equivalent of the corresponding cation to be used is 1 / z.
  • the fragment -COOM of the formula (I) in the case of salt formation stands for the group:
  • physiologically compatible cations are suitable as mono- or polyvalent cations M z + .
  • these are metal cations of the physiologically acceptable metals from the groups Ia, Ib, IIa, IIb, IIIb, Via or VIII of the Periodic Table of the Elements, ammonium ions, as well as cationic organic compounds with quaternized nitrogen atom.
  • the latter are formed for example by protonation of primary, secondary or tertiary organic amines with an acid, such as with compounds of formula (I) in their acidic form, or by permanent quaternization of said organic amines.
  • these cationic organic ammonium compounds are 2-ammonioethanol and 2-trimethylammonioethanol.
  • M or M 'in the formulas (I) preferably represents a hydrogen atom, an ammonium ion, an alkali metal ion, half an equivalent of an alkaline earth metal ion or half an equivalent of a zinc ion, more preferably a hydrogen atom, an ammonium ion, a sodium ion, a potassium ion , Calcium ion, magnesium ion or zinc ion.
  • the compounds of formula (I) are preferably selected from at least one compound from the group formed from N-lauroyl sarcosine, N-myristoyl sarcosine, N-palmitoyl sarcosine, N-oleyl sarcosine, N-cocoyl sarcosine (wherein here is a mixture of compounds and cocoyl corresponds to the composition of the fatty acid cut of coconut oil), N-palm kernel sarcosine (wherein there is a mixture of compounds and palm kernel corresponds to the fatty acid cut composition of palm kernel oil), N-lauroylglutamate, N-myristoylglutamate, N-palmitoylglutamate, N-oleylglutamate, N Cocoylglutamate (in which case a mixture of compounds is present and cocoy
  • the compounds of the formula (I) are selected from at least one compound selected from N-lauroyl sarcosine, N-myristoyl sarcosine, N-palmitoyl sarcosine, N-oleyl sarcosine, N-cocoyl sarcosine (here a mixture of Compounds is present and cocoyl the composition of the fatty acid cut of coconut oil corresponds), N-palm kernel sarcosine (which here is a mixture of compounds and palm kernel corresponds to the composition of the fatty acid cut of palm kernel oil) and the salts (especially the sodium salts) of the aforementioned compounds.
  • N-lauroyl sarcosine N-myristoyl sarcosine, N-palmitoyl sarcosine, N-oleyl sarcosine, N-cocoyl sarcosine (here a mixture of Compounds is present and cocoyl the composition of the
  • the triglycerides of coconut oil have the following fatty acid composition:
  • the triglycerides of palm kernel oil have the following fatty acid composition:
  • compositions of the invention contain the compounds of formula (I) preferably in an amount of 0.05 to 2.0 wt .-%, in particular from 0.1 to 1, 5 wt .-%, each based on the total weight of the composition.
  • n 1
  • R of the formula (II) for a (C 8 to C 2 2) alkyl group or a mono- or polyunsaturated (C 8 to C 2 2) alkenyl group, particularly preferably for a (C 8 to C 2 2) alkyl group.
  • Particularly preferred radicals R of the formula (II) are selected from at least one radical of the group formed from octyl, decyl, dodecyl, tetradecyl, hexadecyl, octadec-9-en-1-yl and octadecyl.
  • the compounds of the formula (II) are selected from one or more representatives of the group which is formed from salts of the sulfoacetic acid dodecyl ester, salts of the sulfoacetic acid ester, salts of the sulfoacetic acid tetradecyl ester, salts of the sulfoacetic acid hexadecyl ester, salts of the sulfoacetic acid octadecyl ester.
  • the sodium salts are preferred.
  • the agents according to the invention preferably contain the compounds of the formula (II) in an amount of from 0.05 to 2.0% by weight, in particular from 0.1 to 1.5% by weight, in each case based on the total weight of the composition.
  • the compounds of the formula (I) and the formula (II) are preferably in a weight ratio of
  • polymers are understood to mean compounds which are different from the compounds of the formulas (I) and (II) and which have a molecular weight of at least 10,000 g / mol.
  • the polymers are composed of a plurality of molecules in which one or more kinds of atoms or atomic groupings (so-called constitutive units, basic building blocks or repeating units) are repeatedly arranged in a row.
  • the polymers are obtained by polyreaction, the latter being synthetic (i.e., synthetic) or natural.
  • Firming polymers contribute to the maintenance and / or build-up of the hair volume and hair fullness of the overall hairstyle. These polymers are at the same time also film-forming polymers and therefore generally typical substances for shaping hair treatment agents such as hair fixatives, hair foams, hair waxes, hair sprays.
  • the film formation can be quite selective and connect only a few fibers.
  • Film-forming polymers are polymers which leave a continuous film on the skin, the hair or the nails when drying.
  • film formers can be used in a wide variety of cosmetic products, such as face masks, for example. Make-up, hair fixatives, hair sprays, hair gels, hair waxes, hair treatments, shampoos or nail polishes are used.
  • Film-forming polymers are furthermore understood as meaning those polymers which, when used in 0.01 to 20% strength by weight aqueous, alcoholic or aqueous-alcoholic solution, are capable of depositing a transparent film on the hair.
  • cosmetic products which contain at least one solidifying, non-ionic polymer and / or at least one consolidating, cationic polymer are best suited according to the invention.
  • the polymers in particular the setting polymers, are particularly preferred in an amount of 0.1 to 15.0% by weight, in particular of 1.0 to 12.0% by weight, very particularly preferably from 2.0 to 10.0 wt .-%, each based on the weight of the cosmetic composition containing
  • compositions according to the invention contain, as additional fixing polymer, at least one consolidating nonionic polymer.
  • the additional strengthening, nonionic polymers are preferably present in the composition according to the invention in an amount of from 0.1 to 10.0% by weight, particularly preferably from 1.0 to 8.0% by weight. , very particularly preferably from 2.0 wt .-% to 6.0 wt .-%, each based on the weight of the inventive compositions.
  • the setting, nonionic polymers are again preferably selected from at least one polymer of the group being formed
  • Suitable polyvinylpyrrolidones are, for example, commercial products such as Luviskol ® K 90 or Luviskol ® K 85 from BASF SE.
  • Suitable polyvinyl acetate is marketed under the trade name Vinac ® as an emulsion from Air Products.
  • composition comprising at least one polymer selected from the group formed as a solidifying, nonionic polymer
  • those agents according to the invention which, as the consolidating nonionic polymer, are at least one polymer selected from the group which is formed, are in turn preferred polyvinylpyrrolidone,
  • Suitable copolymers of vinylpyrrolidone and vinyl acetate are available, for example under the trademark Luviskol ® VA 37, Luviskol ® VA 55, Luviskol ® VA 64 and Luviskol ® VA 73 from the firm BASF SE.
  • Cationic polymers are to be understood as meaning polymers which have a group in the main and / or side chain which may be “temporary” or “permanent” cationic.
  • "permanently cationic” refers to those polymers which have a cationic group, irrespective of the pH of the agent. These are usually polymers containing a quaternary nitrogen atom, for example in the form of an ammonium group.
  • Preferred cationic groups are quaternary ammonium groups.
  • those polymers in which the quaternary ammonium group is bonded via a C 1-4 hydrocarbon group to a polymer main chain constructed from acrylic acid, methacrylic acid or derivatives thereof have proven to be particularly suitable.
  • a fixing, cationic polymer which is preferably suitable according to the invention is at least one consolidating, cationic polymer which comprises at least one structural element of the formula (M9) and additionally at least one structural element of the formula (M10)
  • R is a hydrogen atom or a methyl group
  • R ', R "and R” independently of one another represent a (C 1 -C 30 ) -alkyl group
  • X is an oxygen atom or a group NH
  • A is an ethane-1,2-diyl group or a propane-1,3-diyl group, 1 or 3 means.
  • At least one amphiphilic, cationic polymer comprising at least one structural unit of the formula (M6) and at least one structural unit of the formula (M2) and, if appropriate, at least one structural unit of the formula (M1) is particularly suitable as a consolidating, cationic polymer suitable
  • R and R 4 independently of one another represent a hydrogen atom or a methyl group
  • a and A 2 are each independently a group of ethane-1, 2-diyl, propane-1, 3-diyl or
  • R 2 , R 3 , R 5 and R 6 independently of one another represent a (C 1 to C 4 ) -alkyl group
  • R 7 is a (C 8 to C 30 ) alkyl group.
  • an agent according to the invention as the above suitable fixing, cationic polymer comprises at least one amphiphilic, cationic polymer comprising at least one structural unit of the formula (M6), at least one structural unit of the formula (M7), at least one structural unit of the formula (M3) and at least one structural unit of the formula (M4
  • R and R 4 independently of one another represent a hydrogen atom or a methyl group
  • X 1 and X 2 independently of one another represent an oxygen atom or a group NH
  • a and A 2 are each independently a group of ethane-1, 2-diyl, propane-1, 3-diyl or
  • RR 22 , RR 33 , RR 55 and IR 6 independently of one another represent a (C 1 to C 4 ) -alkyl group
  • R 7 is a (C 8 to C 30 ) alkyl group contains.
  • physiologically acceptable anions such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • Copolymers of N-vinylpyrrolidone, N- (3-dimethylaminopropyl) methacrylamide and 3- (methacryloylamino) propyl-lauryl-dimethylammonium chloride (INCI name: Polyquaternium-55), which is available, for example, under the trade name Styleze W 10 or W 20 (W 10: 10 wt .-% of active substance or W 20: 20 wt .-% of active substance, in each case in ethanol-water mixture) is sold by the company ISP.
  • Dimethylaminopropyl) methacrylamide and 3- (methacryloylamino) propyl-lauryl dimethylammonium chloride (INCI name: Polyquaternium-69), which, for example, under the trade name AquaStyle ® 300 (28-32 wt .-% active ingredient in ethanol-water mixture) of the Company ISP is distributed.
  • the cationic film-forming and / or cationic fixing polymers are particularly preferably selected from cationic, quaternized cellulose derivatives.
  • Suitable cationic and / or setting polymers are preferably cationic, quaternized cellulose derivatives.
  • Such cationic, quaternized celluloses prove to be particularly advantageous for the purposes of the invention, which carry more than one permanent cationic charge in a side chain.
  • cationic celluloses such cationic celluloses with the INCI name Polyquaternium-4 in turn, are particularly suitable, which are sold for example under the names of Celquat ® H 100, Celquat L 200 ® by the company National Starch.
  • cationic polymers which can be used particularly preferably for the purposes of the invention, there continue to be those cationic fixing copolymers which contain at least one structural element of the formula M1 1)
  • R is a (Ci to C 4 ) -alkyl group, in particular a methyl group, and additionally have at least one further cationic and / or nonionic structural element.
  • physiologically acceptable anions such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • At least one copolymer (c1) is present, which in addition to at least one structural element of the formula (M1 1) additionally comprises a structural element of the formula (M6)
  • R is a (C- ⁇ to C 4 ) alkyl group, in particular a methyl group.
  • the copolymers (c1) are all possible physiologically acceptable anions, such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • physiologically acceptable anions such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • Very particularly preferred cationic fixing polymers as copolymers (c1) contain 10 to 30 mol%, preferably 15 to 25 mol% and in particular 20 mol% of structural units of the formula (M1 1) and 70 to 90 mol%, preferably 75 to 85 mol .-% and in particular 80 mol .-% of structural units of the formula (M6).
  • the copolymers (c1) in addition to polymer units resulting from the incorporation of said structural units of the formula (M1 1) and (M6) in the copolymer, a maximum of 5 wt .-%, preferably at most 1 wt .-% , Contain polymer units due to the incorporation of other monomers.
  • these N-methylvinylimidazole / vinylpyrrolidone copolymers are referred to as Polyquaternium-16, according to INCI Nomenclature and are, for example, from BASF under the trade names Luviquat ® Style , Luviquat.RTM ® FC 370, Luviquat.RTM ® FC 550, FC 905 and Luviquat.RTM ® Luviquat.RTM ® HM 552 available.
  • N-methylvinylimidazole / vinylpyrrolidone copolymers will be used according to INCI. Nomenclature referred to as Polyquaternium-44 and are available for example from BASF under the trade name Luviquat ® UltraCare.
  • the pulverulent compositions according to the invention may also contain copolymers (c2) which, starting from the copolymer (c1), have structural units of the formula (M7) as additional structural units
  • compositions according to the invention are thus characterized in that they comprise as cationic consolidating polymer at least one copolymer (c2) having at least one structural unit of formula (M1 1 -a) and at least one structural unit of formula (M6) and at least one structural unit according to formula (M7)
  • the copolymers (c2) in addition to polymer units resulting from the incorporation of the structural units of the formula (M1 1-a), (M6) and (M7) into the copolymer, a maximum of 5 wt .-%, preferably at most 1 wt .-%, polymer units, which go back to the incorporation of other monomers.
  • the copolymers (c2) are composed exclusively of structural units of the formulas (M1 1-a), (M6) and (M7).
  • component (c2) To compensate for the positive polymer charge of component (c2) are all possible physiologically acceptable anions, such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • physiologically acceptable anions such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • a methosulfate be used refer to those N-methylvinylimidazole / vinylpyrrolidone / vinylcaprolactam copolymers, according to INCI nomenclature as Polyquaternium-46 and are for example available under the trade names Luviquat ® Hold by BASF ,
  • Very particularly preferred copolymers (c2) contain 1 to 20 mol%, preferably 5 to 15 mol% and in particular 10 mol% of structural units of the formula (M1 1-a) and 30 to 50 mol. %, preferably 35 to 45 mol .-% and in particular 40 mol .-% of structural units of formula (M6) and 40 to 60 mol .-%, preferably 45 to 55 mol .-% and in particular 60 mol .-% of structural units according to formula (M7).
  • the pulverulent compositions according to the invention as a consolidating cationic polymer may also contain copolymers (c3) which contain as structural units structural units of the formulas (M1 1-a) and (M6), as well as further structural units from the group of the vinylimidazole units and further structural units from the group of the acrylamide and / or methacrylamide units.
  • compositions according to the invention are characterized in that they contain as additional cationic film-forming and / or cationic setting polymer at least one copolymer (c1) which contains at least one structural unit of formula (M1 1-a) and at least one structural unit of formula (M6) and at least one structural unit according to formula (M10) and at least one structural unit according to formula (M12)
  • the copolymers (c1) in addition to polymer units resulting from the incorporation of said structural units of the formula (M1 1-a), (M6), (M8) and (M12) in the copolymer a maximum of 5 wt .-%, preferably at most 1 wt .-%, contain polymer units, which go back to the incorporation of other monomers.
  • the copolymers (c1) are composed exclusively of structural units of the formula (M1 1-a), (M6), (M8) and (M12).
  • component (c1) To compensate for the positive polymer charge of component (c1) are all possible physiologically acceptable anions, such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • physiologically acceptable anions such as chloride, bromide, hydrogen sulfate, methyl sulfate, ethyl sulfate, tetrafluoroborate, phosphate, hydrogen phosphate, dihydrogen phosphate or p-toluenesulfonate, triflate.
  • a methosulfate be used refer to those N-methylvinylimidazole / vinylpyrrolidone / vinylimidazole / methacrylamide copolymers, according to INCI nomenclature as Polyquaternium-68 and are, for example, from BASF under the tradename Luviquat ® Supreme available.
  • cationic fixing polymers preferably used in the compositions according to the invention are the so-called "temporary cationic" polymers. These polymers usually contain an amino group which, at certain pH values, is present as quaternary ammonium group and thus cationic. Chemically, chitosans are partially deacetylated chitins of different molecular weights.
  • chitosans For the production of chitosans is based on chitin, preferably the shell remains of crustaceans, which are available as cheap raw materials in large quantities.
  • the chitin is usually first deproteinized by the addition of bases, demineralized by the addition of mineral acids and finally deacetylated by the addition of strong bases, wherein the molecular weights can be distributed over a broad spectrum.
  • bases Preferably used are those having a weight average molecular weight of 800,000 to 1,200,000 daltons, a Brookfield viscosity (1 wt% in glycolic acid) below 5000 mPas, a degree of deacetylation in the range of 80 to 88%, and have an ash content of less than 0.3 wt .-%.
  • chitosans in addition to the chitosans as typical biopolymers, cationically derivatized chitosans (such as, for example, quaternization products) or alkoxylated chitosans are also suitable as derivatives of chitosan for the purposes of the invention.
  • cationically derivatized chitosans such as, for example, quaternization products
  • alkoxylated chitosans are also suitable as derivatives of chitosan for the purposes of the invention.
  • Agents preferred according to the invention are characterized in that they comprise as consolidating, cationic polymer at least one neutralization product of chitosan with at least one organic carboxylic acid, in particular formic acid, acetic acid, citric acid, lactic acid, pyrrolidonecarboxylic acid, tartaric acid, glycolic acid, nicotinic acid, hydroxyisobutyric acid, hydroxyisovaleric acid or mixtures of these acids , contain.
  • This neutralization product can be prepared, for example, in an aqueous medium by adding chitosan and the corresponding organic carboxylic acid.
  • Suitable chitosans are, for example, under the trade designations Hydagen ® CMF (1 wt .-% of active substance in aqueous solution with 0.4 wt .-% of glycolic acid, molecular weight 500,000 to 5,000,000 g / mol Cognis), Hydagen ® HCMF (chitosan (80% deacetylated), molecular weight of 50,000 to 1,000,000 g / mol, Cognis), Kytamer ® PC (80 wt .-% of active substance of chitosan pyrolidoncarboxylat (INCI name: chitosan PCA), Amerchol) and Chitolam ® NB / 101 freely available commercially.
  • Hydagen ® CMF (1 wt .-% of active substance in aqueous solution with 0.4 wt .-% of glycolic acid, molecular weight 500,000 to 5,000,000 g / mol Cognis)
  • the chitosans or their derivatives are preferably present in the compositions according to the invention in an amount of from 0.01% by weight to 5.0% by weight, particularly preferably from 0.05% by weight to 2.0% by weight. , very particularly preferably from 0, 1 wt .-% to 1, 0 wt .-%, each based on the weight of the inventive composition.
  • Suitable temporary cationic polymers for the purposes of the invention are likewise those which are not permanently cationic and have at least one structural unit of the formulas (M1-1) to (M1-8)
  • Vinylcaprolactam / vinylpyrrolidone / dimethylaminoethyl methacrylate copolymer for example, INCI name: Vinyl caprolactam / PVP / di-methylaminoethyl methacrylate copolymer (Gaffix ® under the trade name VC 713 ISP)
  • Vinylcaprolactam / vinylpyrrolidone / dimethylaminoethyl methacrylate copolymer for example as a 35-39% solids in ethanol in the form of the commercial product Advantage LC E with the INCI Name: Vinyl Caprolactam / VP / Dimethylaminoethyl Methacrylate Copolymer, Alcohol, Lauryl Pyrrolidone (ISP)),
  • Vinylpyrrolidone / dimethylaminopropylmethacrylamide copolymer for example INCI name: VP / DMAPA Acrylates Copolymer under the trade name Styleze CC-10 (ISP)
  • ISP Styleze CC-10
  • compositions of the invention compounds of structural units * - (CH 2 CH 2 0) n - with n> 1 and / or * - (CH 2 CHMeO) m - * with m> 1 in amounts of from 0 to 0.01 wt .-%, in particular from 0 to 0.0001 wt .-%.
  • the agents according to the invention are particularly preferably free of compounds with the abovementioned structural units.
  • Preferred agents are further characterized in that the (C 4 to C 6 ) alkanediols are selected from at least one alkanediol of the group formed from 1, 2-butanediol, 1, 3-butanediol, 2,3-butanediol, 2 Methyl 2,4-butanediol, 1,4-butanediol, 2-methyl-2,4-pentanediol, 1,2-pentanediol, 1,5-pentanediol, 1,2-hexanediol, 1,6-hexanediol, 1 , 2-heptanediol, 1, 7-heptanediol, 1, 2-octanediol, 1, 8-octanediol.
  • Particularly suitable according to the invention is 1, 2-pentanediol.
  • the cosmetic compositions contain the (C 4 to C 6 ) -alkanediols, based on the total weight of the composition, preferably in an amount of from 0.05 to 2.0% by weight, particularly preferably from 0.1% by weight to 1, 5% by weight.
  • compositions according to the invention additionally comprise at least one (C 8 to C 2 o) monocarboxylic acid compound of the formula (III)
  • R is a saturated or unsaturated (C 7 to d 9 ) hydrocarbon radical
  • M n + is an n-valent cation and n is the number 1, 2 or 3 (especially 1).
  • M n + according to formula (III) is preferably selected from metal cations of the physiologically acceptable metals of groups Ia, Ib, IIa, IIb, IIIb, Via or VIII of the Periodic Table of the Elements, ammonium ions and cationic organic compounds having a quaternized nitrogen atom.
  • M n + H +
  • R is according to formula (III) is preferably an unsaturated (C 7 to C 9) hydrocarbon radical.
  • the (C 8 to C 2 o) -monocarboxylic acid compounds of the formula (III) according to the invention are preferably present in the composition according to the invention in an amount of 0.005 to 0.3% by weight, particularly preferably 0.01 to 0.2% by weight. %, in each case based on the weight of the agent according to the invention.
  • the agents according to the invention additionally comprise at least one compound of the formula (IV)
  • M and M 'independently of one another denote a hydrogen atom or one equivalent of a mono- or polyvalent cation
  • n 1 or 2 (in particular 1).
  • a particularly preferred compound of the formula (IV) is a salt of sulfoacetic acid, in particular disodium sulfoacetate.
  • the compounds of the formula (IV) according to the invention are preferably present in the composition according to the invention in an amount of from 0.005% by weight to 0.3% by weight, particularly preferably from 0.1 to 0.2% by weight, based in each case on the weight of the agent according to the invention.
  • compositions of the invention contain water as part of a cosmetically acceptable carrier. It is preferred according to the invention if it is a water-containing cosmetic carrier or an aqueous-alcoholic cosmetic carrier.
  • the agent according to the invention particularly preferably contains at least 50% by weight of water, based on the total weight of the agent.
  • aqueous-alcoholic carriers are to be understood as meaning aqueous compositions containing from 3 to 70% by weight of a C 1 -C 4 -alcohol, in particular ethanol or isopropanol.
  • the compositions according to the invention may additionally contain other organic solvents, such as, for example, methoxybutanol, benzyl alcohol, ethyl diglycol, 1, 2 Propylene glycol or 1, 3-propylene glycol. Preference is given to all water-soluble organic solvents.
  • the inventive agent for increasing the hair care effect may additionally contain at least one cationic surfactant.
  • cationic surfactants are understood in the context of the invention, no polymers.
  • cationic surfactants are especially quaternary ammonium compounds having one or two (C 8 to C 2 o) alkyl. Preference is given to ammonium halides, in particular chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkyl methylammonium chlorides, eg.
  • esterquats such as those marketed under the trademarks Dehyquart ® and Stepantex ® methyl hydroxyalkyl dialkoyloxyalkyl ammonium methosulfate, be used as said quaternary ammonium compounds.
  • the agents according to the invention preferably additionally contain at least one oil body.
  • Oil bodies are at pH 7 and 25 ° C in 100 g of water to not more than 0, 1 g of soluble compounds.
  • the natural and synthetic cosmetic oil bodies are preferred to include:
  • oils examples include sunflower oil, olive oil, soybean oil, rapeseed oil, almond oil, jojoba oil, orange oil, wheat germ oil, peach kernel oil and the liquid portions of coconut oil. Also suitable, however, are other triglyceride oils such as the liquid portions of beef tallow as well as synthetic triglyceride oils.
  • Di-n-alkyl ethers having a total of from 12 to 36 carbon atoms, in particular 12 to 24 carbon atoms, such as di-n-octyl ether, di-n-decyl ether, di-n-nonyl ether, di-n-undecyl ether, di n-dodecyl ether, n-hexyl n-octyl ether, n-octyl n-decyl ether, n-decyl n-undecyl ether, n-undecyl n-dodecyl ether and n-hexyl n-undecyl ether and di-tert-butyl ether , Di-iso-pentyl ether, di-3-ethyldecyl ether, tert-butyl-n-octyl ether, iso-pentyl-n-o
  • the compounds are available as commercial products 1, 3-di- (2-ethylhexyl) -cyclohexane (Cetiol ® S), and di-n-octyl ether (Cetiol ® OE) may be preferred.
  • Ester oils are to be understood as meaning the esters of C 6 - C 30 fatty acids with C 2 - C 30 fatty alcohols.
  • the monoesters of the fatty acids with alcohols having 2 to 24 carbon atoms are preferred.
  • isopropyl myristate IPM Rilanit ®
  • isononanoic acid C16-18 alkyl ester Cetiol ® SN
  • 2-ethylhexyl palmitate Cegesoft ® 24
  • stearic acid-2-ethylhexyl ester (Cetiol ® 868)
  • cetyl oleate glycerol tricaprylate, Kokosfettalkohol- caprinatV caprylate (Cetiol LC), n-butyl stearate, oleyl erucate (Cetiol J 600), isopropyl palmitate (Rilanit ® IPP), Oleyl
  • Dicarboxylic acid esters such as di-n-butyl adipate, di- (2-ethylhexyl) adipate, di- (2-ethylhexyl) succinate and di-isotridecyl acelate
  • diol esters such as ethylene glycol dioleate, ethylene glycol diisotridecanoate, propylene glycol di (2- ethylhexanoate), propylene glycol diisostearate,
  • Fatty acid partial glycerides which are understood to mean monoglycerides, diglycerides and their technical mixtures. With the use of technical products production reasons may still contain small amounts of triglycerides.
  • the partial glycerides preferably follow the formula (D4-I),
  • R, R 2 and R 3 independently of one another represent hydrogen or a linear or branched, saturated and / or unsaturated acyl radical having 6 to 22, preferably 12 to 18, carbon atoms, with the proviso that at least one of these groups represents an acyl radical and at least one of these groups is hydrogen.
  • the sum (m + n + q) is 0 or numbers from 1 to 100, preferably 0 or 5 to 25.
  • R is an acyl radical and R 2 and R 3 are hydrogen and the sum (m + n + q ) is 0.
  • Typical examples are mono- and / or diglycerides based on caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, Elaeostearic acid, arachidic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures.
  • oleic acid monoglycerides are used, perfume,
  • the natural and synthetic cosmetic oil bodies include, for example: vegetable oils.
  • vegetable oils examples include sunflower oil, olive oil, soybean oil, rapeseed oil, almond oil, jojoba oil, orange oil, wheat germ oil, peach kernel oil and the liquid portions of the oil Coconut oil.
  • triglyceride oils such as the liquid portions of beef tallow as well as synthetic triglyceride oils.
  • the compounds are available as commercial products 1, 3-di- (2-ethyl-hexyl) -cyclohexane (Cetiol ® S), and di-n-octyl ether (Cetiol ® OE) may be preferred.
  • Ester oils are to be understood as meaning the esters of C 6 - C 30 fatty acids with C 2 - C 30 fatty alcohols.
  • the monoesters of the fatty acids with alcohols having 2 to 24 carbon atoms are preferred.
  • isopropyl myristate IPM Rilanit ®
  • isononanoic acid C16-18 alkyl ester Cetiol ® SN
  • 2-ethylhexyl palmitate Cegesoft ® 24
  • stearic acid-2-ethylhexyl ester (Cetiol ® 868)
  • cetyl oleate glycerol tricaprylate, Kokosfettalkohol- caprinatV caprylate (Cetiol ® LC), n-butyl stearate, oleyl erucate (Cetiol ® J 600), isopropyl palmitate (Rilanit ® IPP
  • Dicarboxylic acid esters such as di-n-butyl adipate, di- (2-ethylhexyl) adipate, di- (2-ethylhexyl) succinate and di-isotridecyl acelate
  • diol esters such as ethylene glycol dioleate, ethylene glycol diisotridecanoate, propylene glycol di (2- ethylhexanoate), propylene glycol diisostearate,
  • Fatty acid partial glycerides which are understood to mean monoglycerides, diglycerides and their technical mixtures. With the use of technical products production reasons may still contain small amounts of triglycerides.
  • the partial glycerides preferably follow the formula (D4-I),
  • R, R 2 and R 3 independently of one another represent hydrogen or a linear or branched, saturated and / or unsaturated acyl radical having 6 to 22, preferably 12 to 18, carbon atoms, with the proviso that at least one of these groups represents an acyl radical and at least one of these groups is hydrogen.
  • the sum (m + n + q) is 0 or numbers from 1 to 100, preferably 0 or 5 to 25.
  • R is an acyl radical and R 2 and R 3 are hydrogen and the sum (m + n + q ) is 0.
  • Typical examples are mono- and / or diglycerides based on caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmitic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, Elaeostearic acid, arachidic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures.
  • oleic acid monoglycerides are used.
  • the silicones are selected from at least one member of the list formed from:
  • polyalkyl siloxanes polyaryl siloxanes, polyalkylaryl siloxanes which are volatile or nonvolatile, straight chain, branched or cyclic, crosslinked or uncrosslinked;
  • grafted silicone polymers having a non-silicone-containing organic backbone consisting of an organic backbone formed from organic monomers containing no silicone to which at least one polysiloxane macromer has been grafted in the chain and optionally at least one chain end;
  • Particularly preferred cosmetic or dermatological preparations according to the invention are characterized in that they contain at least one silicone of the formula (Si-1)
  • x is a number from 0 to 100, preferably from 0 to 50, more preferably from
  • the inventively preferred cosmetic or dermatological preparations contain a silicone of the above formula (Si-1). These silicones are referred to as dimethicones according to the INCI nomenclature.
  • the silicone of the formula (Si-1) the compounds are preferably: (CH 3 ) 3 Si-O-Si (CH 3 ) 3 , (CH 3 ) 3 Si-O- (CH 3 ) 2 Si-O-Si (CH 3 ) 3, (CH 3 ) 3 Si [O- (CH 3 ) 2 Si] 2 -O-Si (CH 3 ) 3, (CH 3 ) 3 Si [0- ( CH 3 ) 2 Si] 3 -O-Si (CH 3 ) 3 , (CH 3 ) 3 Si [0- (CH 3 ) 2 Si] 4 -O-Si (CH 3 ) 3, (CH 3 ) 3 Si [0- (CH 3 ) 2 Si] 5 -O-Si (CH 3 ) 3, (CH 3 ) 3 Si [0- (CH 3 ) 3 Si [0- (
  • mixtures of o.g. Silicones may be included in the preferred compositions of the invention.
  • Preferred silicones which can be used according to the invention have viscosities of 0.2 to 2 mm 2 s -1 at 20 ° C., silicones having viscosities of 0.5 to 1 mm 2 s -1 being particularly preferred.
  • Particularly preferred agents according to the invention contain one or more amino-functional silicones.
  • Such silicones may e.g. by the formula (Si-2)
  • R is a hydrocarbon or a hydrocarbon radical having from 1 to about 6
  • Q is a polar radical of the general formula -R HZ, wherein
  • R is a divalent linking group bonded to hydrogen and the radical Z composed of carbon and hydrogen atoms, carbon, hydrogen and oxygen atoms or carbon, hydrogen and nitrogen atoms, and
  • Z is an organic, amino-functional group containing at least one amino-functional group
  • b takes values in the range of about 1 to about 3,
  • a + b is less than or equal to 3
  • c is a number in the range of about 1 to about 3, and
  • x is a number ranging from 1 to about 2,000, preferably from about 3 to about 50, and most preferably from about 3 to about 25, and
  • y is a number in the range of from about 20 to about 10,000, preferably from about 125 to about
  • M is a suitable silicone end group, as is known in the art, preferably trimethylsiloxy.
  • Non-limiting examples of the groups represented by R in formula (Si-2) include alkyl groups such as methyl, ethyl, propyl, isopropyl, isopropyl, butyl, isobutyl, amyl, isoamyl, hexyl, isohexyl and the like; Alkenyl radicals such as vinyl, halovinyl, alkylvinyl, allyl, haloallyl, alkylallyl; Cycloalkyl radicals such as cyclobutyl, cyclopentyl, cyclohexyl and the like; Phenyl radicals, benzyl radicals, halohydrocarbon radicals such as 3-chloropropyl, 4-bromobutyl, 3,3,3-trifluoropropyl, chlorocyclohexyl, bromophenyl, chlorophenyl and the like, and sulfur containing radicals such as mercaptoethyl, mer
  • R examples include methylene, ethylene, propylene, hexamethylene, decamethylene, - CH 2 CH (CH 3 ) CH 2 -, phenylene, naphthylene, -CH 2 CH 2 SCH 2 CH 2 -, -CH 2 CH 2 OCH 2 -, -OCH 2 CH 2 -, - OCH 2 CH 2 CH 2 -, -CH 2 CH (CH 3 ) C (O) 2 -, - (CH 2 ) 3 CC (O) 2 CH 2 -, -C 6 H 4 C 6 H 4 -, -C 6 H 4 CH 2 C 6 H 4 -; and - (CH 2 ) 3 C (O) SCH 2 CH 2 -.
  • Z is according to formula (Si-2) an organic, amino-functional radical containing at least one functional amino group.
  • a possible formula for said Z is NH (CH 2 ) Z NH 2 , where z is an integer greater than or equal to 1.
  • Another possible formula for said Z is -NH (CH 2 ) Z (CH 2 ) ZZ NH, wherein both z and zz independently of one another are an integer greater than or equal to 1, this structure comprising diamino ring structures, such as piperazinyl.
  • Said Z is most preferably an -NHCH 2 CH 2 NH 2 radical.
  • Z is -N (CH 2 ) Z (CH 2 ) ZZ NX 2 or -NX 2 , wherein each X is independently selected from X 2 the group consisting of hydrogen and alkyl groups having 1 to 12 carbon atoms, and zz is 0.
  • Q according to formula (Si-2) is most preferably a polar amino-functional radical of formula - CH 2 CH 2 CH 2 NHCH 2 CH 2 NH 2 .
  • ⁇ assumes values in the range of 0 to 2
  • b takes values in the range of 2 to 3
  • a + b is less than or equal to 3
  • c is a number in the range of 1 to 3.
  • the molar ratio of R a Q b SiO (. 4 a - b) / 2 units to R c SiO (4 _ C) / 2 units in the formula (Si-2) is in the range of about 1: From 2 to 1: 65, preferably from about 1: 5 to about 1:65, and most preferably from about 1:15 to about 1: 20. If one or more of the above formula (Si-2) silicones are used then the various variable substituents in the above formula may be different for the various silicone components present in the silicone blend.
  • Preferred cosmetic or dermatological preparations according to the invention contain an amino-functional silicone of the formula (Si-3)
  • G is -H, phenyl, -OH, -O-CH 3 , -CH 3 , -O-CH 2 CH 3 , -CH 2 CH 3 , -O-CH 2 CH 2 CH 3 , -CH 2 CH 2 CH 3 , -O -CH (CH 3 ) 2 , -CH (CH 3 ) 2 , -O-CH 2 CH 2 CH 2 CH 3 , -CH 2 CH 2 CH 2 CH 3 , -O-CH 2 CH (CH 3 ) 2 , -CH 2 CH (CH 3 ) 2 , -O-CH (CH 3 ) CH 2 CH 3 , -CH (CH 3 ) CH 2 CH 3 , -O-C (CH 3 ) 3 , -C (CH 3 ) 3 ;
  • a is a number between 0 and 3, in particular 0;
  • b stands for a number between 0 and 1, in particular 1,
  • n and n are numbers whose sum (m + n) is between 1 and 2000, preferably between 50 and 150, where n is preferably values from 0 to 1999 and in particular from 49 to 149 and m preferably values from 1 to 2000, in particular from 1 to 10,
  • R ' is a monovalent radical selected from
  • each Q is a chemical bond, -CH 2 -, -CH 2 -CH 2 -, -CH 2 CH 2 CH 2 -, -C (CH 3 ) 2 -, -CH 2 CH 2 CH 2 CH 2 -, -CH 2 C (CH 3 ) 2 -, -CH (CH 3 ) CH 2 CH 2 -, R "represents identical or different radicals from the group -H, -Phenyl, -benzyl, -CH 2 - CH (CH 3 ) Ph, the Ci -20- alkyl radicals, preferably -CH 3 , -CH 2 CH 3 , -CH 2 CH 2 Cl-I 3 , - CH (CH 3 ) 2 , -CH 2 CH 2 CH 2 H 3 , -CH 2 CH (CH 3 ) 2 , -CH (CH 3 ) CH 2 CH 3 , -C (CH 3 ) 3 , and A represents an anion which is preferably selected from chloride, bromide,
  • Cationic silicone oils are suitable according to the invention, for example the commercially available Dow Corning 929 emulsion (containing a hydroxylamino-modified silicone which is referred to as amodimethicone), DC 2-2078 (manufacturer Dow Corning, INCI name: Aminopropyl Phenyl Trimethicone), DC 5-71 13 (manufacturer Dow Corning, INCI name: Silicone Quaternium 16), SM-2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil ® Quat 3270 and 3272 (manufacturer: Th. Goldschmidt; diquaternary polydimethylsiloxanes, quaternium-80).
  • Dow Corning 929 emulsion containing a hydroxylamino-modified silicone which is referred to as amodimethicone
  • DC 2-2078 manufactured by Dow Corning 929 emulsion
  • INCI name Aminopropy
  • Particularly preferred agents according to the invention are characterized in that they contain at least one amino-functional silicone of the formula (Si 3-a)
  • silicones are referred to as trimethylsilylamodimethicones according to the INCI declaration and are available, for example, under the name Q2-7224 (manufacturer: Dow Corning, a stabilized trimethylsilylamodimethicone).
  • compositions according to the invention which contain at least one amino-functional silicone of the formula (Si-3b)
  • R- [Si (CH 3) 2 -0] n1 [Si (R ') - 0] m - [Si (CH3) 2-0] n-2 SiMe 2 R (Si-3b), contain, in which R is -OH, a (optionally ethoxylated and / or propoxylated) (Ci to C 20 ) -
  • R ' for -OH, a (C- ⁇ to C 2 o) alkoxy group or a -CH 3 group
  • n1 and n2 are numbers whose sum (m + n1 + n2) is between 1 and 2000, preferably between 50 and 150, the sum (n1 + n2) preferably having values from 0 to 1999 and in particular from 49 to 149 and m preferably values of
  • silicones are according to the INCI declaration as Amodimethicone, or as functionalized Amodimethicone, such as bis (C13-15 alkoxy) PG Amodimethicone (for example, as a commercial product: DC 8500 from Dow Corning available), trideceth-9 PG-amodimethicones (for example as a commercial product Silcare Silicone SEA available from Clariant).
  • Amodimethicone or as functionalized Amodimethicone, such as bis (C13-15 alkoxy) PG Amodimethicone (for example, as a commercial product: DC 8500 from Dow Corning available), trideceth-9 PG-amodimethicones (for example as a commercial product Silcare Silicone SEA available from Clariant).
  • amino-functional silicones preference is given to cosmetic or dermatological preparations according to the invention which contain an amino-functional silicone whose amine number is above 0.25 meq / g, preferably above 0.3 meq / g and in particular above 0.4 meq / g is.
  • the amine number stands for the milliequivalents of amine per gram of the amino-functional silicone. It can be determined by titration and also expressed in mg KOH / g.
  • Agents which are likewise preferred according to the invention are characterized in that they contain at least one silicone of the formula (Si-5)
  • R 3 is -Si- [O-SiR 2] x- (CH 2 ) n - [O-SiR 2 ] y -O-SiR 3 (Si-5),
  • R is identical or different radicals from the group -H, -phenyl, -benzyl, -CH 2 -CH (CH 3 ) Ph, the Ci -2 o-alkyl radicals, preferably -CH 3 , -CH 2 CH 3 , -CH 2 CH 2 CH 3 , -CH (CH 3 ) 2 , -CH 2 CH 2 CH 2 H 3 , -CH 2 CH (CH 3 ) 2 , -CH (CH 3 ) CH 2 CH 3 , - C (CH 3 ) 3 , x and y are a number from 0 to 200, preferably from 0 to 10, more preferably from 0 to 7 and especially 0, 1, 2, 3, 4, 5 or 6, stand and n is a number from 0 to 10, preferably from 1 to 8 and in particular from 2, 3, 4, 5, 6.
  • the silicones are preferably water-soluble. According to preferred means of the embodiment with a silicone are characterized in that the silicone c2) is water-soluble.
  • the oil particles are preferably present in an amount of from 0.05 to 20% by weight, in particular from 0.1 to 20% by weight.
  • the agents according to the invention are preferably present as foam.
  • the compositions according to the invention are filled into a pressurized gas container with a dispenser ("aerosol container").
  • the pressurized gas containers with the aid of which a product is distributed by the internal gas pressure of the container via a valve, are defined as "aerosol containers"
  • a container is defined under normal pressure with the aid of which a product is distributed by means of a mechanical action by means of a pumping or squeezing system
  • the agent according to the invention of this embodiment preferably contains at least one propellant.
  • suitable propellants are for example selected from N 2 0, dimethyl ether, C0 2 , air, alkanes having 3 to 5 carbon atoms, such as propane, n-butane, isobutane, n-pentane and iso-pentane, and their mixtures.
  • alkanes, mixtures of said alkanes or mixtures of said alkanes with dimethyl ether are used as sole blowing agent.
  • the invention expressly also includes the concomitant use of propellants of the type of chlorofluorocarbons, but in particular of fluorocarbons.
  • Butane according to the invention is understood to mean n-butane, isobutane and mixtures of n-butane and isobutane.
  • the agents according to the invention preferably contain the propellant in amounts of from 1 to 35% by weight, based on the total agent. Amounts of 2 to 30 wt .-%, in particular from 3 to 15 wt .-% are particularly preferred.
  • isopentane is preferably suitable as a propellant, which is incorporated into the compositions according to the invention and is packaged in the first chamber of the two-chamber aerosol container.
  • the second Chamber of the two-chamber aerosol container is made up of at least one other, different from isopentane propellant, which builds up a higher pressure in the two-chamber aerosol container than the isopentane.
  • the blowing agents of the second chamber are preferably selected from N 2 O, dimethyl ether, C0 2 , air, alkanes having 3 or 4 carbon atoms (such as propane, n-butane, iso-butane) and mixtures thereof.
  • a second subject of the invention is the use of a cosmetic agent of the first subject of the invention for the temporary reshaping and / or shape fixing of keratinous fibers, in particular human hair.
  • a third object of the invention is a method for the temporary transformation of keratinous fibers, in particular human hair, characterized in that a cosmetic agent of the first subject of the invention is applied to the keratinic fibers.
  • the keratinic fibers are not rinsed and left on the fiber after the action of the cosmetic compositions of the first subject of the invention.
  • the preferred embodiments of the first subject invention apply mutatis mutandis.
  • the formulations E1 and E2 were each filled into an aerosol container, which fulfills the following technical parameters: Aluminum storage container with valve Product 522983 PV10697 from Pecision (Deutsche refzisions-Ventil GmbH).
  • the aerosol container was filled with a propellant gas mixture of propane / butane (47% by weight of propane, 50% by weight of butane, 3% by weight of isobutane), resulting in a weight ratio of formulation to propellant gas of 92 to 8.
  • the agents E1 and E2 were storage stable. When actuated, the aerosol container provided a stable foam which broke on the hair when applied. It was obtained a durable styling with good hair care.

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Abstract

Agents cosmétiques pour le traitement cosmétique de fibres kératiniques, notamment de cheveux humains, contenant i) au moins un composé de formule (I), dans laquelle R1 représente un radical hydrocarboné saturé ou insaturé, linéaire ou ramifié, R2 représente un atome d'hydrogène, un groupe alkyle (C1 à C4) ou un groupe hydroxyalkyle (C2 à C4), R3 représente un atome d'hydrogène ou un groupe (AA), n = 1 ou 2, les radicaux M représentant indépendamment les uns des autres un atome d'hydrogène ou un équivalent d'un cation monovalent ou multivalent, et ii) au moins un composé de formule (II), les radicaux M représentant indépendamment les uns des autres un atome d'hydrogène ou un équivalent d'un cation monovalent ou multivalent, n vaut 1 ou 2 et R1 représente un groupe alkyle (C8 à C22), un groupe alcényle (C8 à C22) monoinsaturé ou polyinsaturé ou un groupe R2-(O-CH2CH2)m-*, dans lequel m est un nombre entier compris entre 1 et 20, notamment entre 1 et 10, et R2 représente un groupe alkyle (C8 à C22) ou un groupe alcényle (C8 à C22) monoinsaturé ou polyinsaturé, et iii) au moins un polymère fixant, et iv) de l'eau. Ces agents cosmétiques sont stables au stockage et permettent d'obtenir une coiffure durable et un bon soin capillaire.
PCT/EP2012/072343 2011-12-19 2012-11-12 Agent cosmétique pour la mise en forme temporaire de fibres kératiniques WO2013091999A2 (fr)

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DE201110089028 DE102011089028A1 (de) 2011-12-19 2011-12-19 Kosmetisches Mittel zur temporären Umformung keratinischer Fasern
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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1994017783A2 (fr) * 1993-02-03 1994-08-18 Unilever Plc Composition nettoyante
US5374420A (en) * 1993-01-22 1994-12-20 Revlon Consumer Products Corporation Hair setting compositions
EP2286908A2 (fr) * 2010-11-19 2011-02-23 Symrise AG Agent de solubilisation pour préparations cosmétiques

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE19756454C1 (de) 1997-12-18 1999-06-17 Henkel Kgaa Verwendung von Glycerincarbonat

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5374420A (en) * 1993-01-22 1994-12-20 Revlon Consumer Products Corporation Hair setting compositions
WO1994017783A2 (fr) * 1993-02-03 1994-08-18 Unilever Plc Composition nettoyante
EP2286908A2 (fr) * 2010-11-19 2011-02-23 Symrise AG Agent de solubilisation pour préparations cosmétiques

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