WO2000061101A1 - Aqueous cosmetic preparations containing tartaric-acid or citric-acid esters of alkyl polyglucose and cationic or amphoteric polymers - Google Patents

Aqueous cosmetic preparations containing tartaric-acid or citric-acid esters of alkyl polyglucose and cationic or amphoteric polymers Download PDF

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Publication number
WO2000061101A1
WO2000061101A1 PCT/EP2000/002969 EP0002969W WO0061101A1 WO 2000061101 A1 WO2000061101 A1 WO 2000061101A1 EP 0002969 W EP0002969 W EP 0002969W WO 0061101 A1 WO0061101 A1 WO 0061101A1
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Prior art keywords
acid
composition according
group
hair
alkyl
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PCT/EP2000/002969
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German (de)
French (fr)
Inventor
Jens Meyer
Dieter Goddinger
Winfried Seidel
Joachim-Kurt Foitzik
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Hans Schwarzkopf Gmbh & Co. Kg
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Priority to AU45424/00A priority Critical patent/AU4542400A/en
Publication of WO2000061101A1 publication Critical patent/WO2000061101A1/en

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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/37Esters of carboxylic acids
    • A61K8/375Esters of carboxylic acids the alcohol moiety containing more than one hydroxy group
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/604Alkylpolyglycosides; Derivatives thereof, e.g. esters
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/73Polysaccharides
    • A61K8/731Cellulose; Quaternized cellulose derivatives
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/72Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds
    • A61K8/84Cosmetics or similar toiletry preparations characterised by the composition containing organic macromolecular compounds obtained by reactions otherwise than those involving only carbon-carbon unsaturated bonds
    • A61K8/89Polysiloxanes
    • A61K8/896Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate
    • A61K8/898Polysiloxanes containing atoms other than silicon, carbon, oxygen and hydrogen, e.g. dimethicone copolyol phosphate containing nitrogen, e.g. amodimethicone, trimethyl silyl amodimethicone or dimethicone propyl PG-betaine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q5/00Preparations for care of the hair
    • A61Q5/02Preparations for cleaning the hair
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54Polymers characterized by specific structures/properties
    • A61K2800/542Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5426Polymers characterized by specific structures/properties characterized by the charge cationic
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/54Polymers characterized by specific structures/properties
    • A61K2800/542Polymers characterized by specific structures/properties characterized by the charge
    • A61K2800/5428Polymers characterized by specific structures/properties characterized by the charge amphoteric or zwitterionic

Definitions

  • the invention relates to aqueous cosmetic compositions for the treatment of hair or skin, which are formulated on a mild surfactant basis, and to the use of these compositions for cleaning hair and skin.
  • agents with certain mild surfactants in combination with cationic polymers are both extremely mild and have excellent product performance.
  • hair that is cleaned with appropriate shampoos has excellent properties in terms of volume, shine, combability, grip and "body”.
  • the invention therefore relates to aqueous cosmetic compositions for treating the hair or the skin on a mild surfactant base, which contain as surfactant at least one ester of a hydroxy-substituted bicarbonic acid or tricarboxylic acid (A) with the general formula (I),
  • YH or -OH is, provided that X is when X is -CH 2 COOR, R, R 1 and R 2 independently of one another are a hydrogen atom, an alkali metal or alkaline earth metal cation, an ammonium group, the cation of an ammonium organic Base or a radical Z which is derived from a polyhydroxylated organic compound which is selected from the group consisting of etherified (C 6 -C 18 ) alkyl polysaccharides with 1 to 6 monomeric saccharide units and etherified aliphatic (C 6 -C 16 ) hydroxyalkyl Polyols having 2 to 16 hydroxyl radicals, is selected, under the condition that at least one of the groups R, R 1 or R 2 is a Z radical and at least one polymer (B) selected from cationic polymers and amphopolymer.
  • R, R 1 and R 2 independently of one another are a hydrogen atom, an alkali metal or alkaline earth metal cation, an ammoni
  • the compounds of the formula (I) are, for example, from European patent EP-B1-0 258 814 and from the articles by N. Burns, Drag Cosmet. Ind. 160 (3), 42 (1997) and T. Verzotti et al., Cosmetic News XX-112, 29 (1997).
  • this prior art does not provide any indication of the agents according to the invention.
  • R, R 1 and R 2 preferably represent alkali metal cations, in particular the sodium ion, alkaline earth metal cations, in particular the magnesium ion, and the ammonium ion.
  • the group Z is preferably an etherified (C 6 -C 18 ) alkyl polysaccharide.
  • Group Z preferably contains glucose as the saccharide.
  • C 6 -C 6 alkyl groups in particular are used as alkyl groups, the choice of unbranched saturated groups being preferred.
  • the alkyl groups can, however, also be mixtures which are obtained when natural fats and oils are processed. Mixtures consisting essentially of
  • C 8 -C 16 alkyl groups can be preferred according to the invention.
  • a mixture of alkyl groups such as is obtained when coconut oil is processed, is very particularly preferred.
  • Group Z contains 1 to 6 monomeric saccharide units. According to a preferred embodiment, the group Z contains 2 to 6 glucose units. However, it may also be preferred to use groups Z with 1.2 to 3, in particular 1.3 to 2, glucose units. It should be noted that mixtures always arise in the synthesis, and these numerical values are derived from the stoichiometric ratio of the starting substances fatty alcohol and saccharide.
  • the compounds according to formula (I) are derivatives of citric acid, tartaric acid or malic acid. Such compounds which are derivatives of citric acid and in particular tartaric acid are preferred according to the invention.
  • the agents according to the invention can of course also contain more than one surfactant (A) of the formula (I).
  • the agents according to the invention preferably contain the compounds of formula (I) in amounts of 0.5 to 8.0% by weight, particularly preferably in amounts of 1 to 5% by weight and in particular in amounts of about 2 to 3% by weight. -%, each based on the total mean.
  • the agents according to the invention contain a polymer (B) as a second mandatory component.
  • the agents according to the invention contain a cationic polymer as polymer (B).
  • the permanent cationic polymers are preferred among the cationic polymers.
  • polymers which have a cationic group irrespective of the pH of the agent are referred to as “permanently cationic” usually polymers that have a quaternary nitrogen atom, for example in the form of a
  • Preferred cationic polymers are, for example, quaternized cellulose derivatives, such as are available under the names of Celquat ® and Polymer JR ® commercially.
  • the compounds Celquat ® H 100, Celquat ® L 200 and Polymer JR ® 400 are preferred quaternized cellulose derivatives.
  • Polysiloxanes with quaternary groups such as the commercially available products Q2-7224 (manufacturer: Dow Corning; a stabilized trimethylsilylamodimethicone), Dow Corning ® 929 Emulsion (containing a hydroxylamino-arnino- modified silicone, which is also referred to as amodimethicone), SM -2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil ® -Quat 3270 and 3272 (manufacturer: Th. Goldschmidt; diquaternary polydimethylsiloxanes, Quaternium-80),
  • Cationic guar derivatives such as in particular the products sold under the trade names Cosmedia ® Guar and Jaguar ® ,
  • Polymeric dimethyldiallylammonium salts and their copolymers with esters and amides of acrylic acid and methacrylic acid Under the names Merquat ® 100 (Poly (dimethyldiallylammonium chloride)) and Merquat ® 550 (dimethyl diallylarnmoniumchlorid-acrylamide copolymer) commercially available products are examples of such cationic polymers.
  • Copolymers of vinyl pyrrolidone with quaternized derivatives of dialkylamino acrylate and methacrylate such as, for example, vinyl pyrrolidone-dimethylaminomethacrylate copolymers quaternized with diethyl sulfate.
  • vinyl pyrrolidone-dimethylaminomethacrylate copolymers quaternized with diethyl sulfate are commercially available under the names Gafquat ® 734 and Gafquat ® 755.
  • Vinylpyrrolidone methoimidazolinium chloride copolymers such as those sold under the name Luviquat ®, quaternized polyvinyl alcohol and under the designations Polyquaternium 2, Polyquaternium 17, Polyquaternium 18 and Polyquaternium 27 known polymers with quaternary nitrogen atoms in the main polymer chain.
  • Cationic polymers preferred according to the invention are quaternized cellulose derivatives and polymeric dimethyldiallylammonium salts and their copolymers.
  • Cationic cellulose derivatives, in particular the commercial product Polymer ® JR 400, are very particularly preferred cationic polymers.
  • ampho-polymers are also suitable as polymers (B).
  • amphopolymer refers to amphoteric polymers, i.e. Polymers that contain both free amino grappes and free -COOH or S ⁇ 3H groups in the molecule and to form internal ones
  • Salts are capable, zwitterionic polymers which contain quaternary ammonium groups and -COO " or -SO3 ' groups in the molecule, and those polymers which contain -COOH or S ⁇ 3H groups and quaternary ammonium groups.
  • amphopolymer suitable is that available under the name Amphomer ® acrylic resin, the methacrylate is a copolymer of tert.-butylamino, N- (1,1,3,3-tetramethylbutyl) -acrylamide and two or more monomers from the group Acrylic acid, methacrylic acid and their simple esters.
  • amphopolymers are composed of unsaturated carboxylic acids (for example acrylic and methacrylic acid), cationically derivatized unsaturated carboxylic acids (for example acrylamidopropyl-trimethyl-ammonium chloride) and optionally other ionic or nonionic monomers, as described, for example, in German Offenlegungsschrift 39 29 973 and can be found in the prior art cited there.
  • Terpolymers of acrylic acid, methyl acrylate and memacrylamidopropyltrimonium chloride, as are commercially available under the name Merquat ® 2001 N are particularly preferred amphopolymers according to the invention.
  • the polymers (B) are preferred in the preparations according to the invention in amounts of 0.05 to 5% by weight. based on the entire preparation. Amounts of 0.1 to 2% by weight are particularly preferred.
  • the agents according to the invention contain water as the third mandatory component.
  • the agents according to the invention usually have a pH in the range from 2 to 9. Agents with pH values in the range from 3 to 7, in particular in the range from 4 to 5.5, can be preferred in the context of the teaching according to the invention.
  • any acid or base that can be used for cosmetic purposes can be used to adjust this pH.
  • an acid it may be preferred to use an acid from the group of the edible acids such as, for example, acetic acid, lactic acid, tartaric acid, citric acid, malic acid, ascorbic acid and gluconic acid.
  • citric acid and lactic acid is particularly preferred.
  • the cosmetic agent is not subject to any restrictions.
  • the mildness of the preparations according to the invention is particularly effective in agents for treating the hair and skin, in particular for cleaning and maintaining the hair and skin.
  • the agent according to the invention is a hair cleanser (shampoo), a shower bath, a foam bath or a liquid soap.
  • shampoos and shower baths are preferred representatives of this embodiment.
  • the shampoos, shower baths, foam baths and liquid soaps according to the invention preferably contain at least one further cleaning component. This is selected in particular from the group of anionic, ampholytic, zwitterionic and nonionic surfactants; However, according to a further embodiment, it can also be cationic surfactants.
  • Suitable anionic surfactants in agents according to the invention are all anionic surface-active substances suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as. B. a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 10 to 22 carbon atoms.
  • the molecule can contain glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups.
  • suitable anionic surfactants are, in each case in the form of the sodium, potassium, magnesium and ammonium as well as the mono-, di- and trialkanolammomium salts with 2 or 3 carbon atoms in the alkanol group,
  • Ether carboxylic acids of the formula RO- (CH2-CH2 ⁇ ) ⁇ -CH2-COOH, in which R is a linear
  • amide ether carboxylates of the formula [R-NH (-CH 2 -CH 2 -O) n -CH 2 -COO] m Z, in which R is for one linear or branched, saturated or unsaturated acyl radical with 2 to 29 C atoms, n for integers from 1 to 10, m for the numbers 1 or 2 and Z for a cation from the group of alkali or alkaline earth metals, acyl sarcosides with 10 up to 18 C atoms in the acyl group, acyl taurides with 10 to 18 C atoms in the acyl group, acyl isethionates with 10 to 18 C atoms in the acyl group,
  • Esters of tartaric acid and citric acid with alcohols the addition products of about 2-15 molecules of ethylene oxide and / or propylene oxide to fatty alcohols with 8 to 22 carbon atoms, coconut monoglyceride sulfates.
  • Preferred anionic surfactants are alkyl sulfates, alkyl polyglycol ether sulfates and ether carboxylic acids with 10 to 18 carbon atoms in the alkyl group and up to 12 glycol ether groups in the molecule, and sulfosuccinic acid and dialkyl esters with 8 to 18 carbon atoms in the alkyl group and sulfosuccinic acid mono- alkyl polyoxyethyl ester with 8 to 18 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups.
  • Non-ionic surfactants contain z.
  • B a polyol group, a polyalkylene glycol ether group or a combination of polyol and polyglycol ether group.
  • Such connections are, for example
  • Preferred nonionic surfactants are alkyl polyglycosides of the general formula RO- (S) ⁇ . These connections are characterized by the following parameters.
  • the alkyl radical R contains 6 to 22 carbon atoms and can be either linear or branched. Primary linear and methyl-branched aliphatic radicals in the 2-position are preferred. Examples of such alkyl radicals are 1-octyl, 1-decyl, 1-lauryl, 1-myristyl, 1-cetyl and 1-stearyl. 1-Octyl, 1-decyl, 1-lauryl, 1-myristyl are particularly preferred. When using so-called "oxo alcohols" as starting materials, compounds with an odd number of carbon atoms in the alkyl chain predominate.
  • the alkyl polyglycosides which can be used according to the invention can contain, for example, only a certain alkyl radical R. Usually, however, these compounds are made from natural fats and oils or mineral oils. In this case, the alkyl radicals R are mixtures corresponding to the starting compounds or corresponding to the respective working up of these compounds.
  • Any mono- or oligosaccharides can be used as sugar building block S.
  • Sugar with 5 or 6 carbon atoms and the corresponding oligosaccharides are usually used.
  • sugars are glucose, fructose, galactose. Arabinose, ribose, xylose, lyxose, allose, old rose, marmose, gulose, idose, talose and sucrose.
  • Preferred sugar building blocks are glucose. Fructose, galactose, arabinose and sucrose; Glucose is particularly preferred.
  • alkyl polyglycosides which can be used according to the invention contain an average of 1.1 to 5 sugar units. Alkyl polyglycosides with x values from 1.1 to 1.6 are preferred. Alkyl glycosides in which x is 1.1 to 1.4 are very particularly preferred.
  • the alkyl glycosides can also serve to improve the fixation of the fragrance components on the hair.
  • the person skilled in the art will preferably resort to this substance class as a further ingredient of the preparations according to the invention.
  • alkoxylated homologs of the alkyl polyglycosides mentioned can also be used according to the invention. These homologues can contain an average of up to 10 ethylene oxide and / or propylene oxide units per alkyl glycoside unit.
  • the compounds with alkyl groups used as surfactants can each be uniform substances. However, it is generally preferred to start from natural vegetable or animal raw materials in the production of these substances, so that substance mixtures with different alkyl chain lengths depending on the respective raw material are obtained.
  • both products with a "normal” homolog distribution and those with a narrowed homolog distribution can be used.
  • “Normal” homolog distribution is understood to mean mixtures of homologues which are obtained as catalysts when converting fatty alcohol and alkylene oxide using alkali metals, alkali metal hydroxides or alkali metal alcoholates.
  • narrow homolog distributions are obtained if, for example, hydrotalcites, alkaline earth metal salts of ether carboxylic acids, alkaline earth metal oxides, hydroxides or alcoholates are used as catalysts become. The use of products with a narrow homolog distribution can be preferred.
  • zwitterionic surfactants can be used, in particular as co-surfactants.
  • Zwitterionic surfactants are surface-active compounds that contain at least one quaternary ammonium group and at least one in the molecule
  • Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example the cocoalkyl-dimethylammonium glycinate, N-acyl-aminopropyl-N, N-dimethyl-ammonium glycinate, for example the cocoacylaminopropyl-dimethylammonium glycinate.
  • a preferred zwitterionic surfactant is the fatty acid amide derivative known under the INCI name Cocamidopropyl Betaine.
  • Ampholytic surfactants are also particularly suitable as co-surfactants.
  • Ampholytic surfactants are surface-active compounds which, in addition to a C 8 -C 18 -alkyl or acyl group, contain at least one free amino group and at least one -COOH or -SO H group in the molecule and are capable of forming internal salts .
  • ampholytic surfactants are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkyl sarcosines, 2-alkylamino propionic acids and alkylamino acetic acids, each with approximately 8 to 18 carbon atoms in the alkyl group.
  • Particularly preferred ampholytic surfactants are N-Kokosalkylamino- propionate, cocoacylaminoethyl aminopropionate and C] 2 . ⁇ 8 acyl sarcosine.
  • Examples of the cationic surfactants which can be used in the hair treatment compositions according to the invention are, in particular, quaternary ammonium compounds.
  • Ammonium halides in particular chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides, eg. B. cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, distearyl dimethylammonium chloride. Lauryldimethylammonium chloride, Lauryldimethylbenzylammoniumchlorid and Tricetylmethylammoniumchlorid.
  • the shampoos according to the invention preferably contain the further cleaning components in amounts of from 5.0 to 40% by weight, in particular from 5.0 to 20% by weight, based on the particular preparation.
  • Preparations of particularly great mildness are obtained if, in addition to the surfactants (A), a zwitterionic surfactant, in particular of the betaine type, is used. Anionic and / or nonionic surfactants can then be added as further surfactants.
  • Nonionic surfactants in particular of the alkylglycoside type, have proven to be outstandingly suitable according to the invention.
  • the agents according to the invention preferably also contain at least one organic thickener.
  • Such thickeners are, for example, thickeners such as agar, guar gum, alginates, cellulose ethers, gelatin, pectins and / or xanthan gum.
  • Ethoxylated fatty alcohols in particular those with limited homolog distribution as they are, for example, as a commercial product under the name Arlypon F ® (Henkel) on the market, alkoxylated methyl glucoside, such as the product Glucamate ® DOE 120 (Amerchol) and ethoxylated propylene glycol esters such as the commercial product Antü ® 141 (Goldschmidt) can be preferred organic thickeners.
  • Hair treatment agents can be, for example, shampoos, hair rinses, hair treatments, permanent waving agents (wave lotions, fixatives), hair colorants, hair tinting agents, hair setting agents, hair sprays, hair lotions or hair tip fluids.
  • the preparations can be formulated as solutions, emulsions, gels, creams, aerosols or lotions; they can remain on the hair or, after a short exposure time, which can be preferred, rinsed out again.
  • the agents according to the invention which also serve to treat hair, contain at least one additional conditioning active ingredient.
  • this improves the combability of the hair after the treatment. This is especially recommended for shampoos that are formulated for the "children" target group in order to correspond to the well-known sensitivity of children when combing, especially of wet hair.
  • Protein hydrolyzates in particular elastin, collagen, keratin, milk protein, soy protein, almond protein, pea protein, potato protein, oat protein, corn protein and wheat protein hydrolyzates, their condensation products with fatty acids and quaternized protein hydrolyzates are also suitable as conditioning agents .
  • Products based on plants can be preferred according to the invention.
  • Silicone oils and silicone gums suitable as conditioning agents are, in particular, dialkyl and alkylarylsiloxanes, such as, for example, dimethylpolysiloxane and methylphenylpolysiloxane, and their alkoxylated and quaternized analogs.
  • Examples of such silicones are the products sold by Dow Coming under the names DC 190, DC 200 and DC 1401 and the commercial product Fancorsil ® LIM-1.
  • a suitable anionic silicone oil is the product Dow Coming ® ! 784.
  • alkylamidoamines, especially fatty acid amidoamines such as the stearylamidopropyldimethylamine available under the name Tego Amid ® S 18, are notable for their good biodegradability.
  • estersquats such as the dialkylammonium methosulfates sold under the trademark Stepantex ® and the corresponding products of the Dehyquart ® series are also very readily biodegradable.
  • Preferred vegetable oils and waxes as conditioning agents are jojoba oil, sunflower oil. Orange oil, almond oil, wheat germ oil and peach seed oil. Jojoba oil and orange oil are particularly preferred.
  • the amount of dissolved inorganic salts is limited to less than 2% by weight, in particular less than 0.5% by weight. It should also be noted that such salts are not only e.g. to adjust the viscosity, but can also be introduced by other active ingredients, in particular surfactants.
  • nonionic polymers such as vinylpyrrolidone / vinyl acrylate copolymers, polyvinylpyrrolidone and vinylpyrrolidone / vinyl acetate copolymers, anionic polymers such as polyacrylic and polymethacrylic acids, their salts, their copolymers with acrylic and methacrylic acid esters and - amides and their derivatives, which are obtained by crosslinking with polyfunctional agents, polyoxycarboxylic acids, such as polyketo and polyaldehydocarboxylic acids and their salts, and polymers and copolymers of crotonic acid with esters and amides of acrylic and methacrylic acid, such as vinyl acetate-crotonic acid and vinyl acetate.
  • nonionic polymers such as vinylpyrrolidone / vinyl acrylate copolymers, polyvinylpyrrolidone and vinylpyrrolidone / vinyl acetate copolymers
  • anionic polymers such as polyacrylic and polymeth
  • Vinyl propionate-crotonic acid copolymers such as glucose and maleic acid, hair-conditioning compounds such as phospholipids, for example soy lecithin, egg lecithin and cephalins, other perfume oils, in particular those with the fragrance note of a cargo, such as apple, bime. Strawberry. Peach apricot. Pineapple, banana. Cherry. Kiwi, mango, coconut. Almond, grapefruit. Passion fruit, tangerine and melon, or the scent of a luxury, such as tobacco, cola. Chewing gum, guarana, chocolate. Cocoa, vanilla. Sarsaparilla, peppermint and rum. Dimethyl isosorbide and cyclodextrins,
  • Solubilizers such as ethanol, isopropanol, ethylene glycol, propylene glycol, glycerin, diethylene glycol and ethoxylated triglycerides, dyes,
  • Anti-dandruff agents such as climbazole, piroctone olamine and zinc omadine, active agents such as bisabolol, allantoin, panthenol, niacinmid, tocopherol and plant extracts,
  • Consistency enhancers such as sugar esters, polyol esters or polyol alkyl ethers, fats and waxes such as walrus, beeswax, montan wax, paraffins, esters, glycerides and fatty alcohols, fatty acid alkanolamides,
  • Complexing agents such as EDTA, NTA, ⁇ -alaninediacetic acid and phosphonic acids, swelling and penetration substances such as PCA, glycerol, propylene glycol monoethyl ether, carbonates, hydrogen carbonates, guanidines, ureas and primary, secondary and tertiary phosphates,
  • Opacifiers such as latex or styrene / acrylamide copolymers, pearlescent agents such as ethylene glycol mono- and distearate or PEG-3 distearate, direct dyes so-called coupler and developer components as oxidation dye precursors,
  • Reducing agents such as Thioglycolic acid and its derivatives, thiolactic acid, cytamine, thio malic acid and ⁇ -mercaptoethanesulfonic acid, oxidizing agents such as hydrogen peroxide, potassium bromate and sodium bromate, blowing agents such as propane-butane mixtures, N2O, dimethyl ether, CO2 and air and
  • Antioxidants Bitter substances such as Denatonium Benzoate, preservatives.
  • the invention also relates to the use of an agent according to one of claims 1 to 10 for cleaning skin and hair.
  • N, N-Dimethyl-N-coconut amidopropylammonium acetobetaine (approx. 30% active substance in water; INCI name: Cocamidopropyl betaine) (CLARIANT) N-coconut fatty acid amidoethyl-N-2-hydroxyethylglycine sodium salt (approx. 50% active substance in water; INCI name : Disodium Cocoamphodiacetate) (WITCO) neutralized ester of alkyl polyglucose with tartaric acid (approx. 30% active substance in water; ⁇ NCI name (provisional): Sodium Cocopolyglucose Tartrate) (CESALPINIA) neutralized ester of alkyl polyglucose with citric acid (approx. 30% active substance in water ; ⁇ NCI name (provisional): Sodium Cocopolyglucose Citrate) (CESALPINIA)
  • HOFFMANN LA-ROCHE quaternized hydroxyethyl cellulose (INCI name: Polyquaternium-10) (AMERCHOL)
  • Dimethyldiallylammonium chloride-acrylamide copolymer (approx. 9% active substance in water; INCI name: Polyquaternium-7) (MERCK)
  • Wheat protein hydrolyzate (approx. 18% active substance; INCI name: Hydrolyzed Wheat Protein) (DGF STOESS) Silicone emulsion (INCI name: Dimethiconol (and) TEA-Dodecylbenzenesulfonate) (CALGON)

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  • Cosmetics (AREA)

Abstract

The invention relates to aqueous cosmetic preparations for the treatment of the hair or skin, on the basis of a mild surface-active agent. Said preparations contain: as surface-active agent at least one ester of a hydroxy-substituted bi- or tricarboxylic acid (A) of general formula (I), in which X is H or a CH2COOR group; Y is H or OH, provided that Y is H if X is CH2COOR; R, R?1 and R2¿ independently of each other are a hydrogen atom, an alkali or alkaline earth metal cation, an ammonium group, the cation of an ammonium-organic base or a rest Z which stems from a polyhydroxylated organic compound selected from the group comprising etherified (C¿6?-C18)-alkyl polysaccharides with between 1 and 6 monomeric saccharide units and etherified aliphatic (C6-C16)-hydroxyalkyl polyols with between 2 and 16 hydroxyl rests, provided that at least one of the groups R, R?1 or R2¿ is a rest Z; and at least one polymer (B) selected from the cationic polymers and amphoteric polymers. The above preparations are characterized by exceptional mildness and highly effect.

Description

WASSRIGES KOSMETISCHES MITTEL, WELCHES WEINSAURE- ODER ZITRONENSÄURE-ESTER DER ALKYLPOLYGLUKOSE UND KATIONISCHE ODER AMPHOTERE POLYMERE ENTHÄLTAQUEOUS COSMETIC AGENT, WHICH CONTAINS VINYL ACID OR CITRIC ACID ESTER OF ALKYL POLYGLUCOSIS AND CATIONIC OR AMPHOTHERIC POLYMERS
Die Erfindung betrifft wäßrige kosmetische Mittel zur Behandlung der Haare oder der Haut, die auf einer milden Tensidgrundlage formuliert sind, sowie die Nerwendung dieser Mittel zur Reinigung von Haaren und Haut.The invention relates to aqueous cosmetic compositions for the treatment of hair or skin, which are formulated on a mild surfactant basis, and to the use of these compositions for cleaning hair and skin.
Die Reinigung und Pflege von Haut und Haaren sowie die dekorative Gestaltung der Frisur sind wichtige Bestandteile der menschlichen Körperpflege. Entsprechend groß sind die Bemühungen, sowohl dem Friseur als auch dem Endverbraucher in jeder Hinsicht optimierte Produkte zur Verfügung zu stellen. Ein Schwerpunkt der Entwicklungsarbeit liegt dabei selbstverständlich bei den eigentlichen Produkteigenschaften, sei es die Reinigungswirkung eines Shampoos, eines Duschbades oder eine Flüssigseife, die Pflegewirkung einer Haarkur oder Hautcreme, die Färbeeigenschaften eines Färbemittels oder einer Tönung, die Qualität einer Dauerwelle oder der Frisurenhalt eines Festigers oder Haarsprays. Gleichzeitig wird auch versucht, möglichen unerwünschten Nebenwirkungen, wie sie bei bestimmten Verbrauchergruppen wie beispielsweise Allergikern oder sehr empfindlichen Personen auftreten können, in immer höherem Maße vorzubeugen. Dies führte beispielsweise zur Entwicklung besonders hautfreundlicher Tensidsysteme für reinigende Mittel. Insbesondere besteht ein Wunsch, bei Produkten, die im Rahmen der Anwendung auch unbeabsichtigt mit den Augen in Kontakt kommen können, Formulierungen auf Basis sehr milder Inhaltsstoffe bereitzustellen.The cleaning and care of skin and hair as well as the decorative design of the hairstyle are important components of human body care. The efforts to make optimized products available to the hairdresser as well as the end user are correspondingly great. One focus of the development work is of course on the actual product properties, be it the cleaning effect of a shampoo, a shower bath or a liquid soap, the care effect of a hair treatment or skin cream, the coloring properties of a colorant or a tint, the quality of a perm or the hairstyle hold of a setting or Hair sprays. At the same time, attempts are increasingly being made to prevent possible undesirable side effects, such as can occur in certain consumer groups such as allergy sufferers or very sensitive people. This led, for example, to the development of particularly skin-friendly surfactant systems for cleaning agents. In particular, there is a desire to provide formulations based on very mild ingredients for products that can also come into contact with the eyes unintentionally as part of the application.
Solche sehr milden Mittel werden vom Verbraucher aber dann nicht akzeptiert, wenn andere wesentliche Produkteigenschaften deutlich schlechter sind oder als schlechter angesehen werden. So schäumen Shampoos auf Basis sehr milder Tensidmischungen in vielen Fällen deutlich weniger. Eine große Schaummenge wird vom Verbraucher aber sehr häufig mit einer guten Reinigungswirkung gleichgesetzt, so daß er hier Defizite sieht. Weiterhin erwecken Haare, die mit solchen mild formulierten Shampoos gewaschen werden, häufig einen stumpfen Eindruck. Gleiches gilt beispielsweise auch für Duschbäder.Such very mild agents are not accepted by the consumer if other essential product properties are significantly worse or are considered to be worse. In many cases, shampoos based on very mild surfactant mixtures foam significantly less. A large amount of foam is often equated by the consumer with a good cleaning effect, so that he sees deficits here. Farther Hair that is washed with such mildly formulated shampoos often gives a dull impression. The same applies, for example, to shower rooms.
Es besteht daher nach wie vor die Aufgabe, Mittel zur Behandlung von Haaren und Haut bereitzustellen, die sich einerseits durch eine sehr milde Tensidbasis, andererseits aber auch durch exzellente Produktleistungen auszeichnen.It is therefore still the task to provide agents for the treatment of hair and skin which are distinguished on the one hand by a very mild surfactant base and on the other hand by excellent product performance.
Es wurde nun überraschenderweise gefunden, daß Mittel mit bestimmten milden Tensiden in Kombination mit kationischen Polymeren sowohl äußerst milde sind als auch hervorragende Produktleistungen aufweisen. So weisen beispielsweise Haare, die mit entsprechenden Shampoos gereinigt werden, exzellente Eigenschaften hinsichtlich Volumen, Glanz, Kämmbarkeit, Griff und „body" auf.It has now surprisingly been found that agents with certain mild surfactants in combination with cationic polymers are both extremely mild and have excellent product performance. For example, hair that is cleaned with appropriate shampoos has excellent properties in terms of volume, shine, combability, grip and "body".
Gegenstand der Erfindung sind daher wäßrige kosmetische Mittel zur Behandlung der Haare oder der Haut auf einer milden Tensidgrundlage, die enthalten als Tensid mindestens einen Ester einer hydroxysubstituierten Bi- oder Tricarbon- säure (A) mit der allgemeinen Formel (I),The invention therefore relates to aqueous cosmetic compositions for treating the hair or the skin on a mild surfactant base, which contain as surfactant at least one ester of a hydroxy-substituted bicarbonic acid or tricarboxylic acid (A) with the general formula (I),
XX
II.
HO — C — COOR1 (I)HO - C - COOR 1 (I)
Y — CH — COOR2 Y - CH - COOR 2
in derin the
X H oder eine -CH2COOR-Gruppe ist,XH or a -CH 2 COOR group,
Y H oder -OH ist unter der Bedingung, daß Y H ist, wenn X -CH2COOR ist, R, R1 und R2 unabhängig voneinander ein Wasserstoffatom, ein Alkali- oder Erdalkalimetallkation, eine Ammoniumgruppe, das Kation einer ammonium-orga- nischen Base oder einen Rest Z, der von einer polyhydroxylierten organischen Verbindung stammt, die aus der Gruppe, die veretherte (C6-C18)-Alkyl-Polysaccharide mit 1 bis 6 monomeren Saccharideinheiten und veretherte aliphatische (C6-C16)- Hydroxyalkyl-Polyole mit 2 bis 16 Hydroxylresten umfaßt, ausgewählt ist, bedeuten, unter der Bedingung, daß mindestens eine der Gruppen R, R1 oder R2 ein Rest Z ist, und mindestens ein Polymer (B), ausgewählt aus kationischen Polymeren und Ampho- Polymeren.YH or -OH is, provided that X is when X is -CH 2 COOR, R, R 1 and R 2 independently of one another are a hydrogen atom, an alkali metal or alkaline earth metal cation, an ammonium group, the cation of an ammonium organic Base or a radical Z which is derived from a polyhydroxylated organic compound which is selected from the group consisting of etherified (C 6 -C 18 ) alkyl polysaccharides with 1 to 6 monomeric saccharide units and etherified aliphatic (C 6 -C 16 ) hydroxyalkyl Polyols having 2 to 16 hydroxyl radicals, is selected, under the condition that at least one of the groups R, R 1 or R 2 is a Z radical and at least one polymer (B) selected from cationic polymers and amphopolymer.
Die Verbindungen der Formel (I) sind beispielsweise aus der Europäischen Patentschrift EP-B1-0 258 814 sowie aus den Artikeln von N. Burns, Drag Cosmet. Ind. 160(3), 42 (1997) und T. Verzotti et al., Cosmetic News XX-112, 29 (1997) bekannt. Dieser Stand der Technik liefert jedoch keinerlei Hinweise auf die erfindungsgemäßen Mittel.The compounds of the formula (I) are, for example, from European patent EP-B1-0 258 814 and from the articles by N. Burns, Drag Cosmet. Ind. 160 (3), 42 (1997) and T. Verzotti et al., Cosmetic News XX-112, 29 (1997). However, this prior art does not provide any indication of the agents according to the invention.
Die Herstellung der Verbindungen gemäß Formel (I) wird ausführlich in der Europäischen Patentschrift EP -B 1-0 258 814 beschrieben. Bezüglich der einzelnen Vertreter, die durch die allgemeine Formel (I) definiert werden, wird ausdrücklich auf den Inhalt dieser Europäischen Patentschrift, insbesondere die Passage von Seite 2, Zeile 43, bis Seite 5, Zeile 56, Bezug genommen.The preparation of the compounds of the formula (I) is described in detail in European Patent EP -B 1-0 258 814. With regard to the individual representatives defined by the general formula (I), express reference is made to the content of this European patent specification, in particular the passage from page 2, line 43, to page 5, line 56.
Im Rahmen der vorliegenden Erfindung stehen R, R1 und R2 bevorzugt für Alkalimetallkationen, insbesondere das Natriumion, Erdalkalimetallkationen, insbesondere das Magnesiumion, und das Ammoniumion.In the context of the present invention, R, R 1 and R 2 preferably represent alkali metal cations, in particular the sodium ion, alkaline earth metal cations, in particular the magnesium ion, and the ammonium ion.
Die Gruppe Z ist bevorzugt ein verethertes (C6-C18)-Alkyl-Polysaccharid. Als Saccharid enthält die Gruppe Z bevorzugt Glucose.The group Z is preferably an etherified (C 6 -C 18 ) alkyl polysaccharide. Group Z preferably contains glucose as the saccharide.
Als Alkylgruppen werden insbesondere C6-C)6- Alkylgruppen eingesetzt, wobei die Wahl von unverzweigten gesättigten Gruppen bevorzugt ist. Bei den Alkylgruppen kann es sich aber auch um Mischungen handeln, die bei der Verarbeitung natürlicher Fette und Öle erhalten werden. Mischungen, bestehend im wesentlichen ausC 6 -C 6 alkyl groups in particular are used as alkyl groups, the choice of unbranched saturated groups being preferred. The alkyl groups can, however, also be mixtures which are obtained when natural fats and oils are processed. Mixtures consisting essentially of
C8-C10-Alkylgruppen,C 8 -C 10 alkyl groups,
C12-C14-Alkylgrappen oderC 12 -C 14 alkyl groups or
C8-C16-Alkylgruppen können erfindungsgemäß bevorzugt sein. Ganz besonders bevorzugt ist eine Mischung von Alkylgruppen, wie sie bei der Verarbeitung von Kokosöl erhalten wird. Die Gruppe Z enthält 1 bis 6 monomere Saccharideinheiten. Gemäß einer bevorzugten Ausführungsform enthält die Gruppe Z 2 bis 6 Glucoseeinheiten. Es kann aber auch bevorzugt sein, Gruppen Z mit 1,2 bis 3, insbesondere 1,3 bis 2, Glucoseeinheiten einzusetzen. Dabei ist zu berücksichtigen, daß bei der Synthese immer Mischungen entstehen, und diese Zahlenwerte aus dem stöchiometrischen Verhältnis der Ausgangssubstanzen Fettalkohol und Saccharid hergeleitet werden.C 8 -C 16 alkyl groups can be preferred according to the invention. A mixture of alkyl groups, such as is obtained when coconut oil is processed, is very particularly preferred. Group Z contains 1 to 6 monomeric saccharide units. According to a preferred embodiment, the group Z contains 2 to 6 glucose units. However, it may also be preferred to use groups Z with 1.2 to 3, in particular 1.3 to 2, glucose units. It should be noted that mixtures always arise in the synthesis, and these numerical values are derived from the stoichiometric ratio of the starting substances fatty alcohol and saccharide.
Die Verbindungen gemäß Formel (I) sind Derivate der Zitronensäure, der Weinsäure oder der Äpfelsäure. Solche Verbindungen, die Derivate der Zitronensäure und insbesondere der Weinsäure darstellen, sind erfindungsgemäß bevorzugt.The compounds according to formula (I) are derivatives of citric acid, tartaric acid or malic acid. Such compounds which are derivatives of citric acid and in particular tartaric acid are preferred according to the invention.
Handelsprodukte, die von der Firma Cesalpinia unter den Bezeichnungen Eucarol® AGE- ET und Eucarol® AGE-EC vertrieben werden, haben sich als besonders gut geeignete Vertreter der Verbindungen gemäß Formel (I) erwiesen.Commercial products, which are sold by the company Cesalpinia under the names Eucarol ® AGE-ET and Eucarol ® AGE-EC, have proven to be particularly suitable representatives of the compounds of the formula (I).
Selbstverständlich können die erfindungsgemäßen Mittel auch mehr als ein Tensid (A) der Formel (I) enthalten.The agents according to the invention can of course also contain more than one surfactant (A) of the formula (I).
Bevorzugt enthalten die erfindungsgemäßen Mittel die Verbindungen der Formel (I) in Mengen von 0,5 bis 8,0 Gew.-%, besonders bevorzugt in Mengen von 1 bis 5 Gew.-% und insbesondere in Mengen von etwa 2 bis 3 Gew.-%, jeweils bezogen auf das gesamte Mittel.The agents according to the invention preferably contain the compounds of formula (I) in amounts of 0.5 to 8.0% by weight, particularly preferably in amounts of 1 to 5% by weight and in particular in amounts of about 2 to 3% by weight. -%, each based on the total mean.
Als zweiten zwingenden Bestandteil enthalten die erfindungsgemäßen Mittel ein Polymer (B).The agents according to the invention contain a polymer (B) as a second mandatory component.
Gemäß einer ersten, bevorzugten Ausführungsform enthalten die erfindungsgemäßen Mittel als Polymer (B) ein kationisches Polymer.According to a first preferred embodiment, the agents according to the invention contain a cationic polymer as polymer (B).
Unter den kationischen Polymeren sind dabei die permanent kationischen Polymere bevorzugt. Als „permanent kationisch" werden erfindungsgemäß solche Polymeren bezeichnet, die unabhängig vom pH- Wert des Mittels eine kationische Gruppe aufweisen. Dies sind in der Regel Polymere, die ein quartäres Stickstoffatom, beispielsweise in Form einerThe permanent cationic polymers are preferred among the cationic polymers. According to the invention, polymers which have a cationic group irrespective of the pH of the agent are referred to as “permanently cationic” usually polymers that have a quaternary nitrogen atom, for example in the form of a
Ammoniumgruppe, enthalten.Ammonium group.
Bevorzugte kationische Polymere sind beispielsweise quaternisierte Cellulose-Derivate, wie sie unter den Bezeichnungen Celquat® und Polymer JR® im Handel erhältlich sind. Die Verbindungen Celquat® H 100, Celquat® L 200 und Polymer JR®400 sind bevorzugte quaternierte Cellulose-Derivate. Polysiloxane mit quatemären Gruppen, wie beispielsweise die im Handel erhältlichen Produkte Q2-7224 (Hersteller: Dow Corning; ein stabilisiertes Trimethylsilylamodimethicon), Dow Corning® 929 Emulsion (enthaltend ein hydroxyl-arnino- modifiziertes Silicon, das auch als Amodimethicone bezeichnet wird), SM-2059 (Hersteller: General Electric), SLM-55067 (Hersteller: Wacker) sowie Abil®-Quat 3270 und 3272 (Hersteller: Th. Goldschmidt; diquaternäre Polydime- thylsiloxane, Quaternium-80),Preferred cationic polymers are, for example, quaternized cellulose derivatives, such as are available under the names of Celquat ® and Polymer JR ® commercially. The compounds Celquat ® H 100, Celquat ® L 200 and Polymer JR ® 400 are preferred quaternized cellulose derivatives. Polysiloxanes with quaternary groups, such as the commercially available products Q2-7224 (manufacturer: Dow Corning; a stabilized trimethylsilylamodimethicone), Dow Corning ® 929 Emulsion (containing a hydroxylamino-arnino- modified silicone, which is also referred to as amodimethicone), SM -2059 (manufacturer: General Electric), SLM-55067 (manufacturer: Wacker) and Abil ® -Quat 3270 and 3272 (manufacturer: Th. Goldschmidt; diquaternary polydimethylsiloxanes, Quaternium-80),
Kationische Guar-Derivate, wie insbesondere die unter den Handelsnamen Cosmedia®Guar und Jaguar® verriebenen Produkte,Cationic guar derivatives, such as in particular the products sold under the trade names Cosmedia ® Guar and Jaguar ® ,
Polymere Dimethyldiallylammoniumsalze und deren Copolymere mit Estern und Amiden von Acrylsäure und Methacrylsäure. Die unter den Bezeichnungen Mer- quat®100 (Poly(dimethyldiallylammoniumchlorid)) und Merquat®550 (Dimethyl- diallylarnmoniumchlorid-Acrylamid-Copolymer) im Handel erhältlichen Produkte sind Beispiele für solche kationischen Polymere.Polymeric dimethyldiallylammonium salts and their copolymers with esters and amides of acrylic acid and methacrylic acid. Under the names Merquat ® 100 (Poly (dimethyldiallylammonium chloride)) and Merquat ® 550 (dimethyl diallylarnmoniumchlorid-acrylamide copolymer) commercially available products are examples of such cationic polymers.
Copolymere des Vinylpyrrolidons mit quaternierten Derivaten des Dialkylamino- acrylats und -methacrylats, wie beispielsweise mit Diethylsulfat quaternierte Vinyl- pyrrolidon-Dimethylaminomethacrylat-Copolymere. Solche Verbindungen sind unter den Bezeichnungen Gafquat®734 und Gafquat®755 im Handel erhältlich. Vinylpyrrolidon-Methoimidazoliniumchlorid-Copolymere, wie sie unter der Bezeichnung Luviquat® angeboten werden, quaternierter Polyvinylalkohol sowie die unter den Bezeichnungen Polyquaternium 2, Polyquaternium 17, Polyquaternium 18 und Polyquaternium 27 bekannten Polymeren mit quartären Stickstoffatomen in der Polymerhauptkette.Copolymers of vinyl pyrrolidone with quaternized derivatives of dialkylamino acrylate and methacrylate, such as, for example, vinyl pyrrolidone-dimethylaminomethacrylate copolymers quaternized with diethyl sulfate. Such compounds are commercially available under the names Gafquat ® 734 and Gafquat ® 755. Vinylpyrrolidone methoimidazolinium chloride copolymers such as those sold under the name Luviquat ®, quaternized polyvinyl alcohol and under the designations Polyquaternium 2, Polyquaternium 17, Polyquaternium 18 and Polyquaternium 27 known polymers with quaternary nitrogen atoms in the main polymer chain.
Erfindungsgemäß bevorzugte kationische Polymere sind quaternisierte Cellulose-Derivate sowie polymere Dimethyldiallylammoniumsalze und deren Copolymere. Kationische Cellulose-Derivate, insbesondere das Handelsprodukt Polymer®JR 400, sind ganz besonders bevorzugte kationische Polymere.Cationic polymers preferred according to the invention are quaternized cellulose derivatives and polymeric dimethyldiallylammonium salts and their copolymers. Cationic cellulose derivatives, in particular the commercial product Polymer ® JR 400, are very particularly preferred cationic polymers.
Geeignet als Polymere (B) sind auch Ampho-Polymere. Unter dem Oberbegriff Ampho- Polymere sind amphotere Polymere, d.h. Polymere, die im Molekül sowohl freie Amino- grappen als auch freie -COOH- oder Sθ3H-Gruppen enthalten und zur Ausbildung innererAmpho-polymers are also suitable as polymers (B). The term amphopolymer refers to amphoteric polymers, i.e. Polymers that contain both free amino grappes and free -COOH or Sθ3H groups in the molecule and to form internal ones
Salze befähigt sind, zwitterionische Polymere, die im Molekül quartäre Ammo- niumgruppen und -COO"- oder -SO3 '-Gruppen enthalten, und solche Polymere zusammengefaßt, die -COOH- oder Sθ3H-Gruppen und quartäre Ammoniumgrappen enthalten.Salts are capable, zwitterionic polymers which contain quaternary ammonium groups and -COO " or -SO3 ' groups in the molecule, and those polymers which contain -COOH or Sθ3H groups and quaternary ammonium groups.
Ein Beispiel für ein erfindungsgemäß einsetzbares Amphopolymer ist das unter der Bezeichnung Amphomer® erhältliche Acrylharz, das ein Copolymer aus tert.-Butylamino- ethylmethacrylat, N-(1,1,3,3-Tetramethylbutyl)acrylamid sowie zwei oder mehr Monomeren aus der Gruppe Acrylsäure, Methacrylsäure und deren einfachen Estern darstellt. Ebenfalls bevorzugte Amphopolymere setzen sich aus ungesättigten Carbonsäuren (z.B. Acryl- und Methacryl-säure), kationisch derivatisierten ungesättigten Carbonsäuren (z.B. Acrylamidopropyl-trimethyl-ammoniumchlorid) und gegebenenfalls weiteren ionischen oder nichtionogenen Monomeren zusammen, wie beispielsweise in der deutschen Offen- legungsschrift 39 29 973 und dem dort zitierten Stand der Technik zu entnehmen sind. Terpolymere von Acrylsäure, Methylacrylat und Memacrylamidopropyltrimoniumchlorid, wie sie unter der Bezeichnung Merquat®2001 N im Handel erhältlich sind, sind erfindungsgemäß besonders bevorzugte Ampho-Polymere. Die Polymere (B) sind in den erfindungsgemäßen Zubereitungen bevorzugt in Mengen von 0,05 bis 5 Gew.-%. bezogen auf die gesamte Zubereitung, enthalten. Mengen von 0,1 bis 2 Gew.-% sind besonders bevorzugt.An example of the present invention amphopolymer suitable is that available under the name Amphomer ® acrylic resin, the methacrylate is a copolymer of tert.-butylamino, N- (1,1,3,3-tetramethylbutyl) -acrylamide and two or more monomers from the group Acrylic acid, methacrylic acid and their simple esters. Likewise preferred amphopolymers are composed of unsaturated carboxylic acids (for example acrylic and methacrylic acid), cationically derivatized unsaturated carboxylic acids (for example acrylamidopropyl-trimethyl-ammonium chloride) and optionally other ionic or nonionic monomers, as described, for example, in German Offenlegungsschrift 39 29 973 and can be found in the prior art cited there. Terpolymers of acrylic acid, methyl acrylate and memacrylamidopropyltrimonium chloride, as are commercially available under the name Merquat ® 2001 N, are particularly preferred amphopolymers according to the invention. The polymers (B) are preferred in the preparations according to the invention in amounts of 0.05 to 5% by weight. based on the entire preparation. Amounts of 0.1 to 2% by weight are particularly preferred.
Als dritte zwingende Komponente enthalten die erfindungsgemäßen Mittel Wasser.The agents according to the invention contain water as the third mandatory component.
Die erfindungsgemäßen Mittel weisen üblicherweise einen pH- Wert im Bereich von 2 bis 9 auf. Mittel mit pH- Werten im Bereich von 3 bis 7, insbesondere im Bereich von 4 bis 5,5, können im Rahmen der erfindungsgemäßen Lehre bevorzugt sein.The agents according to the invention usually have a pH in the range from 2 to 9. Agents with pH values in the range from 3 to 7, in particular in the range from 4 to 5.5, can be preferred in the context of the teaching according to the invention.
Zur Einstellung dieses pH- Wertes kann praktisch jede für kosmetische Zwecke verwendbare Säure oder Base eingesetzt werden. Für den Fall, daß zur pH- Wert-Einstellung eine Säure verwendet wird, kann es bevorzugt sein, eine Säure aus der Gruppe der Genußsäuren wie beispielsweise Essigsäure, Milchsäure, Weinsäure, Zitronensäure, Äpfelsäure, Ascor- binsäure und Gluconsäure zu verwenden. Im Rahmen der Erfindung ist die Verwendung von Zitronensäure und Milchsäure besonders bevorzugt.Virtually any acid or base that can be used for cosmetic purposes can be used to adjust this pH. In the event that an acid is used to adjust the pH, it may be preferred to use an acid from the group of the edible acids such as, for example, acetic acid, lactic acid, tartaric acid, citric acid, malic acid, ascorbic acid and gluconic acid. In the context of the invention, the use of citric acid and lactic acid is particularly preferred.
Das kosmetische Mittel unterliegt erfindungsgemäß keinen Einschränkungen. Es kommen prinzipiell alle auch dem Markt befindlichen Arten von Mitteln, insbesondere die oben genannten Zubereitungen, in Betracht.According to the invention, the cosmetic agent is not subject to any restrictions. In principle, all types of agents also available on the market, in particular the above-mentioned preparations, come into consideration.
Die erfindungsgemäße Milde der Zubereitungen kommt jedoch vor allem in Mitteln zur handlung der Haare und der Haut, insbesondere zur Reinigung und Pflege der Haare und der Haut, zum Tragen.However, the mildness of the preparations according to the invention is particularly effective in agents for treating the hair and skin, in particular for cleaning and maintaining the hair and skin.
Gemäß einer ersten bevorzugten Ausfuhrungsform handelt es sich bei dem erfindungsgemäßen Mittel um ein Haarreinigungsmittel (Shampoo), ein Duschbad, ein Schaumbad oder eine Flüssigseife. Shampoos und Duschbäder sind bevorzugte Vertreter dieser Aus- f hrungsform.According to a first preferred embodiment, the agent according to the invention is a hair cleanser (shampoo), a shower bath, a foam bath or a liquid soap. Shampoos and shower baths are preferred representatives of this embodiment.
Diese Mittel können alle für solche Zubereitungen bekannten weiteren Inhaltsstoffe enthalten. Die erfindungsgemäßen Shampoos, Duschbäder, Schaumbäder und Flüssigseifen enthalten bevorzugt noch mindestens eine weitere reinigende Komponente. Diese wird insbesondere aus der Gruppe der anionischen, ampholytische, zwitterionischen und nichtionogenen Tenside ausgewählt; es kann sich aber auch gemäß einer weiteren Ausführungsform um kationische Tenside handeln.These agents can contain all other ingredients known for such preparations. The shampoos, shower baths, foam baths and liquid soaps according to the invention preferably contain at least one further cleaning component. This is selected in particular from the group of anionic, ampholytic, zwitterionic and nonionic surfactants; However, according to a further embodiment, it can also be cationic surfactants.
Als anionische Tenside eignen sich in erfindungsgemäßen Mitteln alle für die Verwendung am menschlichen Körper geeigneten anionischen oberflächenaktiven Stoffe. Diese sind gekennzeichnet durch eine wasserlöslich machende, anionische Gruppe wie z. B. eine Carboxylat-, Sulfat-, Sulfonat- oder Phosphat-Gruppe und eine lipophile Alkylgruppe mit etwa 10 bis 22 C-Atomen. Zusätzlich können im Molekül Glykol- oder Polyglykolether- Gruppen, Ester-, Ether- und Amidgrappen sowie Hydroxylgruppen enthalten sein. Beispiele für geeignete anionische Tenside sind, jeweils in Form der Natrium-, Kalium-, Magnesium- und Ammonium- sowie der Mono-, Di- und Trialkanolammomumsalze mit 2 oder 3 C-Atomen in der Alkanolgruppe,Suitable anionic surfactants in agents according to the invention are all anionic surface-active substances suitable for use on the human body. These are characterized by a water-solubilizing, anionic group such as. B. a carboxylate, sulfate, sulfonate or phosphate group and a lipophilic alkyl group with about 10 to 22 carbon atoms. In addition, the molecule can contain glycol or polyglycol ether groups, ester, ether and amide groups and hydroxyl groups. Examples of suitable anionic surfactants are, in each case in the form of the sodium, potassium, magnesium and ammonium as well as the mono-, di- and trialkanolammomium salts with 2 or 3 carbon atoms in the alkanol group,
lineare Fettsäuren mit 10 bis 22 C-Atomen (Seifen),linear fatty acids with 10 to 22 carbon atoms (soaps),
Ethercarbonsäuren der Formel R-O-(CH2-CH2θ)χ-CH2-COOH, in der R eine lineareEther carboxylic acids of the formula RO- (CH2-CH2θ) χ -CH2-COOH, in which R is a linear
Alkylgruppe mit 10 bis 22 C-Atomen und x = 0 oder 1 bis 16 ist, Amidethercarboxylate der Formel [R-NH(-CH2-CH2-O)n-CH2-COO]mZ, in der R für einen linearen oder verzweigten, gesättigten oder ungesättigten Acylrest mit 2 bis 29 C-Atomen, n für ganze Zahlen von 1 bis 10, m für die Zahlen 1 oder 2 und Z für ein Kation aus der Gruppe der Alkali- oder Erdalkalimetalle steht, Acylsarcoside mit 10 bis 18 C-Atomen in der Acylgruppe, Acyltauride mit 10 bis 18 C-Atomen in der Acylgruppe, Acylisethionate mit 10 bis 18 C-Atomen in der Acylgruppe,Is alkyl group with 10 to 22 carbon atoms and x = 0 or 1 to 16, amide ether carboxylates of the formula [R-NH (-CH 2 -CH 2 -O) n -CH 2 -COO] m Z, in which R is for one linear or branched, saturated or unsaturated acyl radical with 2 to 29 C atoms, n for integers from 1 to 10, m for the numbers 1 or 2 and Z for a cation from the group of alkali or alkaline earth metals, acyl sarcosides with 10 up to 18 C atoms in the acyl group, acyl taurides with 10 to 18 C atoms in the acyl group, acyl isethionates with 10 to 18 C atoms in the acyl group,
Sulfobernsteinsäuremono- und dialkylester mit 8 bis 18 C-Atomen in der Alkylgruppe und Sulfobernsteinsäuremono-alkylpolyoxyethylester mit 8 bis 18 C-Atomen in der Alkylgrappe und 1 bis 6 Oxyethylgruppen, lineare Alkansulfonate mit 12 bis 18 C-Atomen, lineare Alpha-Olefinsulfonate mit 12 bis 18 C-Atomen, Alpha-Sulfofettsäuremethylester von Fettsäuren mit 12 bis 18 C-Atomen. Alkylsulfate und Alkylpolyglykolethersulfate der Formel R-O(-CH2-CH2θ)χ-Sθ3H, in der R eine bevorzugt lineare Alkylgrappe mit 10 bis 18Sulfosuccinic acid mono- and dialkyl esters with 8 to 18 carbon atoms in the alkyl group and sulfosuccinic acid mono-alkyl polyoxyethyl esters with 8 to 18 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups, linear alkane sulfonates with 12 to 18 carbon atoms, linear alpha-olefin sulfonates with 12 to 18 carbon atoms, alpha-sulfofatty acid methyl esters of fatty acids with 12 to 18 carbon atoms. Alkyl sulfates and alkyl polyglycol ether sulfates of the formula RO (-CH2-CH2θ) χ -Sθ3H, in which R is a preferably linear alkyl group with 10 to 18
C-Atomen und x = 0 oder 1 bis 12 ist,C atoms and x = 0 or 1 to 12,
Gemische oberflächenaktiver Hydroxysulfonate gemäß DE-A-3725 030, sulfatierte Hydroxyalkylpolyethylen- und/oder Hydroxyalkylenpropylenglykolether gemäß DE-A-37 23 354,Mixtures of surface-active hydroxysulfonates according to DE-A-3725 030, sulfated hydroxyalkyl polyethylene and / or hydroxyalkylene propylene glycol ethers according to DE-A-37 23 354,
Sulfonate ungesättigter Fettsäuren mit 12 bis 24 C-Atomen und 1 bis 6 Doppelbindungen gemäß DE-A-39 26 344,Sulfonates of unsaturated fatty acids with 12 to 24 carbon atoms and 1 to 6 double bonds according to DE-A-39 26 344,
Ester der Weinsäure und Zitronensäure mit Alkoholen, die Anlagerungsprodukte von etwa 2-15 Molekülen Ethylenoxid und/oder Propylenoxid an Fettalkohole mit 8 bis 22 C-Atomen darstellen, Kokosmonoglyceridsulfate.Esters of tartaric acid and citric acid with alcohols, the addition products of about 2-15 molecules of ethylene oxide and / or propylene oxide to fatty alcohols with 8 to 22 carbon atoms, coconut monoglyceride sulfates.
Bevorzugte anionische Tenside sind Alkylsulfate, Alkylpolyglykolethersulfate und Ether- carbonsäuren mit 10 bis 18 C-Atomen in der Alkylgrappe und bis zu 12 Glykolether- grappen im Molekül, sowie Sulfobernsteinsäuremono- und -dialkylester mit 8 bis 18 C- Atomen in der Alkylgrappe und Sulfobernsteinsäuremono-alkylpolyoxyethylester mit 8 bis 18 C-Atomen in der Alkylgruppe und 1 bis 6 Oxyethylgruppen.Preferred anionic surfactants are alkyl sulfates, alkyl polyglycol ether sulfates and ether carboxylic acids with 10 to 18 carbon atoms in the alkyl group and up to 12 glycol ether groups in the molecule, and sulfosuccinic acid and dialkyl esters with 8 to 18 carbon atoms in the alkyl group and sulfosuccinic acid mono- alkyl polyoxyethyl ester with 8 to 18 carbon atoms in the alkyl group and 1 to 6 oxyethyl groups.
Nichtionogene Tenside enthalten als hydrophile Gruppe z. B. eine Polyolgruppe, eine Po- lyalkylenglykolethergrappe oder eine Kombination aus Polyol- und Polyglykolether- grappe. Solche Verbindungen sind beispielsweiseNon-ionic surfactants contain z. B. a polyol group, a polyalkylene glycol ether group or a combination of polyol and polyglycol ether group. Such connections are, for example
Anlagerungsprodukte von 2 bis 30 Mol Ethylenoxid und/oder 0 bis 5 Mol Propylenoxid an lineare Fettalkohole mit 8 bis 22 C-Atomen, an Fettsäuren mit 12 bis 22 C- Atomen und an Alkylphenole mit 8 bis 15 C-Atomen in der Alkylgrappe, Ci 2-C22-Fettsäuremono- und -diester von Anlagerungsprodukten von 1 bis 30 MolAddition products of 2 to 30 moles of ethylene oxide and / or 0 to 5 moles of propylene oxide with linear fatty alcohols with 8 to 22 carbon atoms, with fatty acids with 12 to 22 carbon atoms and with alkylphenols with 8 to 15 carbon atoms in the alkyl group, Ci 2-C22-F ett säuremono- and diesters of addition products of 1 to 30 mol
Ethylenoxid an Glycerin,Ethylene oxide on glycerol,
Cg-C22_Nlkylrnono- und -oligoglycoside und deren ethoxylierte Analoga sowie Anlagerungsprodukte von 5 bis 60 Mol Ethylenoxid an Rizinusöl und gehärtetes Rizinusöl.Cg-C22 _ alkyl mono- and oligoglycosides and their ethoxylated analogues as well Addition products of 5 to 60 moles of ethylene oxide with castor oil and hardened castor oil.
Bevorzugte nichtionische Tenside sind Alkylpolyglykoside der allgemeinen Formel RO- (S)χ. Diese Verbindungen sind durch die folgenden Parameter gekennzeichnet.Preferred nonionic surfactants are alkyl polyglycosides of the general formula RO- (S) χ . These connections are characterized by the following parameters.
Der Alkylrest R enthält 6 bis 22 Kohlenstoffatome und kann sowohl linear als auch verzweigt sein. Bevorzugt sind primäre lineare und in 2-Stellung methylverzweigte aliphati- sche Reste. Solche Alkylreste sind beispielsweise 1-Octyl, 1-Decyl, 1-Lauryl, 1-Myristyl, 1-Cetyl und 1-Stearyl. Besonders bevorzugt sind 1-Octyl, 1-Decyl, 1-Lauryl, 1-Myristyl. Bei Verwendung sogenannter "Oxo-Alkohole" als Ausgangsstoffe überwiegen Verbindungen mit einer ungeraden Anzahl von Kohlenstoffatomen in der Alkylkette.The alkyl radical R contains 6 to 22 carbon atoms and can be either linear or branched. Primary linear and methyl-branched aliphatic radicals in the 2-position are preferred. Examples of such alkyl radicals are 1-octyl, 1-decyl, 1-lauryl, 1-myristyl, 1-cetyl and 1-stearyl. 1-Octyl, 1-decyl, 1-lauryl, 1-myristyl are particularly preferred. When using so-called "oxo alcohols" as starting materials, compounds with an odd number of carbon atoms in the alkyl chain predominate.
Die erfindungsgemäß verwendbaren Alkylpolyglykoside können beispielsweise nur einen bestimmten Alkylrest R enthalten. Üblicherweise werden diese Verbindungen aber ausgehend von natürlichen Fetten und Ölen oder Mineralölen hergestellt. In diesem Fall liegen als Alkylreste R Mischungen entsprechend den Ausgangsverbindungen bzw. entsprechend der jeweiligen Aufarbeitung dieser Verbindungen vor.The alkyl polyglycosides which can be used according to the invention can contain, for example, only a certain alkyl radical R. Usually, however, these compounds are made from natural fats and oils or mineral oils. In this case, the alkyl radicals R are mixtures corresponding to the starting compounds or corresponding to the respective working up of these compounds.
Besonders bevorzugt sind solche Alkylpolyglykoside, bei denen RAlkylpolyglycosides in which R
im wesentlichen aus Cg- und C j Q- Alkylgruppen, im wesentlichen aus C^- und C 14- Alkylgruppen, im wesentlichen aus Cg- bis C1 g-Alkylgrappen oder im wesentlichen aus C 12- bis C 1 g-Alkylgrappen besteht.consists essentially of Cg and C j Q alkyl groups, essentially from C ^ and C 14 alkyl groups, essentially from Cg to C1 g alkyl groups or essentially from C 12 to C 1 g alkyl groups.
Als Zuckerbaustein S können beliebige Mono- oder Oligosaccharide eingesetzt werden. Üblicherweise werden Zucker mit 5 bzw. 6 Kohlenstoffatomen sowie die entsprechenden Oligosaccharide eingesetzt. Solche Zucker sind beispielsweise Glucose, Fructose, Galac- tose. Arabinose, Ribose, Xylose, Lyxose, Allose, Altrose, Marmose, Gulose, Idose, Talose und Sucrose. Bevorzugte Zuckerbausteine sind Glucose. Fructose, Galactose, Arabinose und Sucrose; Glucose ist besonders bevorzugt.Any mono- or oligosaccharides can be used as sugar building block S. Sugar with 5 or 6 carbon atoms and the corresponding oligosaccharides are usually used. Examples of such sugars are glucose, fructose, galactose. Arabinose, ribose, xylose, lyxose, allose, old rose, marmose, gulose, idose, talose and sucrose. Preferred sugar building blocks are glucose. Fructose, galactose, arabinose and sucrose; Glucose is particularly preferred.
Die erfindungsgemäß verwendbaren Alkylpolyglykoside enthalten im Schnitt 1,1 bis 5 Zuckereinheiten. Alkylpolyglykoside mit x- Werten von 1,1 bis 1,6 sind bevorzugt. Ganz besonders bevorzugt sind Alkylglykoside, bei denen x 1,1 bis 1,4 beträgt.The alkyl polyglycosides which can be used according to the invention contain an average of 1.1 to 5 sugar units. Alkyl polyglycosides with x values from 1.1 to 1.6 are preferred. Alkyl glycosides in which x is 1.1 to 1.4 are very particularly preferred.
Die Alkylglykoside können neben ihrer Tensidwirkung auch dazu dienen, die Fixierung der Duftkomponenten auf dem Haar zu verbessern. Der Fachmann wird also für den Fall, daß eine über die Dauer der Haarbehandlung hinausgehende Wirkung des Parfumöles auf dem Haar gewünscht wird, bevorzugt zu dieser Substanzklasse als weiterem Inhaltsstoff der erfindungsgemäßen Zubereitungen zurückgreifen.In addition to their surfactant action, the alkyl glycosides can also serve to improve the fixation of the fragrance components on the hair. In the event that an effect of the perfume oil on the hair beyond the duration of the hair treatment is desired, the person skilled in the art will preferably resort to this substance class as a further ingredient of the preparations according to the invention.
Auch die alkoxylierten Homologen der genannten Alkylpolyglykoside können erfindungsgemäß eingesetzt werden. Diese Homologen können durchschnittlich bis zu 10 Ethylenoxid- und/oder Propylenoxideinheiten pro Alkylglykosideinheit enthalten.The alkoxylated homologs of the alkyl polyglycosides mentioned can also be used according to the invention. These homologues can contain an average of up to 10 ethylene oxide and / or propylene oxide units per alkyl glycoside unit.
Bei den als Tenside eingesetzten Verbindungen mit Alkylgruppen kann es sich jeweils um einheitliche Substanzen handeln. Es ist jedoch in der Regel bevorzugt, bei der Herstellung dieser Stoffe von nativen pflanzlichen oder tierischen Rohstoffen auszugehen, so daß man Substanzgemische mit unterschiedlichen, vom jeweiligen Rohstoff abhängigen Alkyl- kettenlängen erhält.The compounds with alkyl groups used as surfactants can each be uniform substances. However, it is generally preferred to start from natural vegetable or animal raw materials in the production of these substances, so that substance mixtures with different alkyl chain lengths depending on the respective raw material are obtained.
Bei den Tensiden, die Anlagerungsprodukte von Ethylen- und/oder Propylenoxid an Fettalkohole oder Derivate dieser Anlagerungsprodukte darstellen, können sowohl Produkte mit einer "normalen" Homologenverteilung als auch solche mit einer eingeengten Homologenverteilung verwendet werden. Unter "normaler" Homologenverteilung werden dabei Mischungen von Homologen verstanden, die man bei der Umsetzung von Fettalkohol und Alkylenoxid unter Verwendung von Alkalimetallen, Alkalimetallhydroxiden oder Alkali- metallalkoholaten als Katalysatoren erhält. Eingeengte Homologenverteilungen werden dagegen erhalten, wenn beispielsweise Hydrotalcite, Erdalkalimetallsalze von Ethercarbon- säuren, Erdalkalimetalloxide, -hydroxide oder -alkoholate als Katalysatoren verwendet werden. Die Verwendung von Produkten mit eingeengter Homologenverteilung kann bevorzugt sein.In the case of the surfactants, which are addition products of ethylene and / or propylene oxide onto fatty alcohols or derivatives of these addition products, both products with a "normal" homolog distribution and those with a narrowed homolog distribution can be used. “Normal” homolog distribution is understood to mean mixtures of homologues which are obtained as catalysts when converting fatty alcohol and alkylene oxide using alkali metals, alkali metal hydroxides or alkali metal alcoholates. By contrast, narrow homolog distributions are obtained if, for example, hydrotalcites, alkaline earth metal salts of ether carboxylic acids, alkaline earth metal oxides, hydroxides or alcoholates are used as catalysts become. The use of products with a narrow homolog distribution can be preferred.
Weiterhin können, insbesondere als Co-Tenside, zwitterionische Tenside verwendet werden. Als zwitterionische Tenside werden solche oberflächenaktiven Verbindungen bezeichnet, die im Molekül mindestens eine quartäre Ammoniumgrappe und mindestens eineFurthermore, zwitterionic surfactants can be used, in particular as co-surfactants. Zwitterionic surfactants are surface-active compounds that contain at least one quaternary ammonium group and at least one in the molecule
-COO - oder -SO -Gruppe tragen. Besonders geeignete zwitterionische Tenside sind die sogenannten Betaine wie die N-Alkyl-N,N-dimethylammonium-glycinate, beispielsweise das Kokosalkyl-dimethylammonium-glycinat, N-Acyl-aminopropyl-N,N-dimethyl- ammoniumglycinate, beispielsweise das Kokosacylaminopropyl-dimethylammonium- glycinat. und 2-Alkyl-3-carboxylmethyl-3-hydroxyethyl-imidazoline mit jeweils 8 bis 18 C-Atomen in der Alkyl- oder Acylgruppe sowie das Kokosacylaminoethylhydroxyethyl- carboxymethylglycinat. Ein bevorzugtes zwitterionisches Tensid ist das unter der INCI-Bezeichnung Cocamidopropyl Betaine bekannte Fettsäureamid-Derivat.Wear a -COO or -SO group. Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example the cocoalkyl-dimethylammonium glycinate, N-acyl-aminopropyl-N, N-dimethyl-ammonium glycinate, for example the cocoacylaminopropyl-dimethylammonium glycinate. and 2-alkyl-3-carboxylmethyl-3-hydroxyethyl-imidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and the cocoacylaminoethylhydroxyethylcarboxymethylglycinate. A preferred zwitterionic surfactant is the fatty acid amide derivative known under the INCI name Cocamidopropyl Betaine.
Ebenfalls insbesondere als Co-Tenside geeignet sind ampholytische Tenside. Unter ampho- lytischen Tensiden werden solche oberflächenaktiven Verbindungen verstanden, die außer einer C 8 -C 18 -Alkyl- oder Acylgruppe im Molekül mindestens eine freie Aminograppe und mindestens eine -COOH- oder -SO H-Grappe enthalten und zur Ausbildung innerer Salze befähigt sind. Beispiele für geeignete ampholytische Tenside sind N-Alkylglycine, N- Alkylpropionsäuren, N-Alkylaminobuttersäuren, N-Alkyliminodipropionsäuren, N-Hy- droxyethyl-N-alkylamidopropylglycine, N-Alkyltaurine, N-Alkylsarcosine, 2-Alkylamino- propionsäuren und Alkylaminoessigsäuren mit jeweils etwa 8 bis 18 C-Atomen in der Alkylgruppe. Besonders bevorzugte ampholytische Tenside sind das N-Kokosalkylamino- propionat, das Kokosacylaminoethylaminopropionat und das C]28-Acylsarcosin.Ampholytic surfactants are also particularly suitable as co-surfactants. Ampholytic surfactants are surface-active compounds which, in addition to a C 8 -C 18 -alkyl or acyl group, contain at least one free amino group and at least one -COOH or -SO H group in the molecule and are capable of forming internal salts . Examples of suitable ampholytic surfactants are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkyl sarcosines, 2-alkylamino propionic acids and alkylamino acetic acids, each with approximately 8 to 18 carbon atoms in the alkyl group. Particularly preferred ampholytic surfactants are N-Kokosalkylamino- propionate, cocoacylaminoethyl aminopropionate and C] 28 acyl sarcosine.
Beispiele für die in den erfindungsgemäßen Haarbehandlungsmitteln verwendbaren kationischen Tenside sind insbesondere quartäre Ammoniumverbindungen. Bevorzugt sind Ammoniumhalogenide, insbesondere Chloride und Bromide, wie Alkyltrimethylammo- niumchloride, Dialkyldimethylammoniumchloride und Trialkylmethylammoniumchloride, z. B. Cetyltrimethylammoniumchlorid, Stearyltrimethylammoniumchlorid, Distearyl- dimethylammoniumchlorid. Lauryldimethylammoniumchlorid, Lauryldimethylbenzyl- ammoniumchlorid und Tricetylmethylammoniumchlorid. Weiterhin können die sehr gut biologisch abbaubaren quatemären Esterverbindungen, wie beispielsweise die unter dem Warenzeichen Stepantex® vertriebenen Dialkylarnmoniummethosulfate und Methyl- hydroxyalkyl-dialkoyloxyalkyl-ammoniummethosulfate und die entsprechenden Produkte der Dehyquart®-Reihe, als kationische Tenside eingesetzt werden. Weitere erfindungsgemäß verwendbare kationische Tenside stellen die quaternisierten Proteinhydrolysate dar.Examples of the cationic surfactants which can be used in the hair treatment compositions according to the invention are, in particular, quaternary ammonium compounds. Ammonium halides, in particular chlorides and bromides, such as alkyltrimethylammonium chlorides, dialkyldimethylammonium chlorides and trialkylmethylammonium chlorides, eg. B. cetyltrimethylammonium chloride, stearyltrimethylammonium chloride, distearyl dimethylammonium chloride. Lauryldimethylammonium chloride, Lauryldimethylbenzylammoniumchlorid and Tricetylmethylammoniumchlorid. May continue to the very readily biodegradable quaternary Esterverbindungen, such as the products marketed under the trademark Stepantex ® Dialkylarnmoniummethosulfate and methyl hydroxyalkyl dialkoyloxyalkyl methosulfates and the corresponding products of Dehyquart ® series, be used as cationic surfactants. The quaternized protein hydrolyzates are further cationic surfactants which can be used according to the invention.
Vorzugsweise enthalten die erfindungsgemäßen Shampoos die weiteren reinigenden Komponenten in Mengen von 5,0 bis 40 Gew.-%, insbesondere von 5,0 bis 20 Gew.-%, bezogen auf die jeweilige Zubereitung.The shampoos according to the invention preferably contain the further cleaning components in amounts of from 5.0 to 40% by weight, in particular from 5.0 to 20% by weight, based on the particular preparation.
Zubereitungen von besonders großer Milde werden dann erhalten, wenn neben den Tensiden (A) ein zwitterionisches Tensid, insbesondere vom Typ der Betaine, verwendet wird. Als weitere Tenside können dann noch anionische und/oder nichtionogene Tenside hinzugefügt werden.Preparations of particularly great mildness are obtained if, in addition to the surfactants (A), a zwitterionic surfactant, in particular of the betaine type, is used. Anionic and / or nonionic surfactants can then be added as further surfactants.
Eine Viererkombination, bestehend ausA combination of four consisting of
Tensiden (A) gemäß Formel (I), zwitterionischen Tensiden, insbesondere vom Typ der Betaine, anionischen Tensiden, insbesondere Alkylethersulfaten und Ethercarbonsäuresalzen, undSurfactants (A) according to formula (I), zwitterionic surfactants, in particular of the betaine type, anionic surfactants, in particular alkyl ether sulfates and ether carboxylic acid salts, and
Niotensiden, insbesondere vom Typ der Alkylglykoside, hat sich als erfindungsgemäß hervorragend geeignet erwiesen.Nonionic surfactants, in particular of the alkylglycoside type, have proven to be outstandingly suitable according to the invention.
Bevorzugt enthalten die erfindungsgemäßen Mittel weiterhin mindestens ein organisches Verdickungsmittel. Solche Verdickungsmittel sind beispielsweise Verdickungsmittel wie Agar-Agar, Guar-Gum, Alginate, Celluloseether, Gelatine, Pektine und/oder Xanthan- Gum. Ethoxilierte Fettalkohole, insbesondere solche mit eingeschränkter Homologenverteilung, wie sie beispielsweise als Handelsprodukt unter der Bezeichnung Arlypon®F (Henkel) auf dem Markt sind, alkoxylierte Methylglucosidester, wie das Handelsprodukt Glucamate® DOE 120 (Amerchol), und ethoxylierte Propylenglykolester, wie das Handelsprodukt Antü® 141 (Goldschmidt) können bevorzugte organische Verdickungsmittel sein.The agents according to the invention preferably also contain at least one organic thickener. Such thickeners are, for example, thickeners such as agar, guar gum, alginates, cellulose ethers, gelatin, pectins and / or xanthan gum. Ethoxylated fatty alcohols, in particular those with limited homolog distribution as they are, for example, as a commercial product under the name Arlypon F ® (Henkel) on the market, alkoxylated methyl glucoside, such as the product Glucamate ® DOE 120 (Amerchol) and ethoxylated propylene glycol esters such as the commercial product Antü ® 141 (Goldschmidt) can be preferred organic thickeners.
Wie bereits oben erwähnt, unterliegen die erfindungsgemäßen Mittel hinsichtlich ihres Verwendungszweckes keinen prinzipiellen Einschränkungen. So kann es sich bei Haarbehandlungsmittel beispielsweise um Shampoos, Haarspülungen, Haarkuren, Dauerwellmittel (Wellotionen, Fixiermittel), Haarfärbemittel, Haartönungsmittel, Haarfestiger, Haarsprays, Haarwässer oder Haarspitzenfluids handeln. Entsprechend dem Verwendungszweck können die Zubereitungen als Lösungen, Emulsionen, Gele, Cremes, Aerosole oder Lotionen formuliert werden; sie können auf dem Haar verbleiben, oder nach einer kurzen Einwirkzeit, was bevorzugt sein kann, wieder ausgespült werden.As already mentioned above, the agents according to the invention are not subject to any fundamental restrictions with regard to their intended use. Hair treatment agents can be, for example, shampoos, hair rinses, hair treatments, permanent waving agents (wave lotions, fixatives), hair colorants, hair tinting agents, hair setting agents, hair sprays, hair lotions or hair tip fluids. Depending on the intended use, the preparations can be formulated as solutions, emulsions, gels, creams, aerosols or lotions; they can remain on the hair or, after a short exposure time, which can be preferred, rinsed out again.
Gemäß einer weiteren bevorzugten Ausführangsform enthalten die erfindungsgemäßen Mittel, die auch der - Haarbehandlung dienen, mindestens einen zusätzlichen konditionierenden Wirkstoff. Dadurch wird insbesondere auch die Kämmbarkeit der Haare nach der Behandlung verbessert. Dies ist speziell für Shampoos zu empfehlen, die für die Zielgruppe „Kinder" formuliert werden, um der bekannten Empfindlichkeit der Kinder beim Kämmen insbesondere des nassen Haares zu entsprechen.According to a further preferred embodiment, the agents according to the invention, which also serve to treat hair, contain at least one additional conditioning active ingredient. In particular, this improves the combability of the hair after the treatment. This is especially recommended for shampoos that are formulated for the "children" target group in order to correspond to the well-known sensitivity of children when combing, especially of wet hair.
Proteinhydrolysate, insbesondere Elastin-, Kollagen-, Keratin-, Milcheiweiß-, Sojaprotein-, Mandelprotein-, Erbsenprotein-, Kartoffelprotein-, Haferprotein-, Maisprotein- und Wei- zenproteinhydrolysate, deren Kondensationsprodukte mit Fettsäuren sowie quaternisierte Proteinhydrolysate sind ebenfalls als konditionierende Wirkstoffe geeignet. Dabei können Produkte auf pflanzlicher Basis erfindungsgemäß bevorzugt sein.Protein hydrolyzates, in particular elastin, collagen, keratin, milk protein, soy protein, almond protein, pea protein, potato protein, oat protein, corn protein and wheat protein hydrolyzates, their condensation products with fatty acids and quaternized protein hydrolyzates are also suitable as conditioning agents . Products based on plants can be preferred according to the invention.
Als konditionierende Wirkstoffe geeignete Silikonöle und Silikon-Gums sind insbesondere Dialkyl- und Alkylarylsiloxane, wie beispielsweise Dimethylpolysiloxan und Methyl- phenylpolysiloxan, sowie deren alkoxylierte und quaternierte Analoga. Beispiele für solche Silikone sind die von Dow Coming unter den Bezeichnungen DC 190, DC 200 und DC 1401 vertriebenen Produkte sowie das Handelsprodukt Fancorsil® LIM-1. Ein geeignetes anionisches Silikonöl ist das Produkt Dow Coming®! 784. Alkylamidoamine, insbesondere Fettsäureamidoamine wie das unter der Bezeichnung Tego Amid®S 18 erhältliche Stearylamidopropyldimethylamin, zeichnen sich neben einer guten konditionierenden Wirkung speziell durch ihre gute biologische Abbaubarkeit aus.Silicone oils and silicone gums suitable as conditioning agents are, in particular, dialkyl and alkylarylsiloxanes, such as, for example, dimethylpolysiloxane and methylphenylpolysiloxane, and their alkoxylated and quaternized analogs. Examples of such silicones are the products sold by Dow Coming under the names DC 190, DC 200 and DC 1401 and the commercial product Fancorsil ® LIM-1. A suitable anionic silicone oil is the product Dow Coming ® ! 784. In addition to a good conditioning effect, alkylamidoamines, especially fatty acid amidoamines such as the stearylamidopropyldimethylamine available under the name Tego Amid ® S 18, are notable for their good biodegradability.
Ebenfalls sehr gut biologisch abbaubar sind quatemäre Esterverbindungen, sogenannte "Esterquats", wie die unter dem Warenzeichen Stepantex® vertriebenen Dialkyl-ammoni- ummethosulfate sowie die entsprechenden Produkte der Dehyquart®-Serie.Quaternary ester compounds, so-called "esterquats", such as the dialkylammonium methosulfates sold under the trademark Stepantex ® and the corresponding products of the Dehyquart ® series are also very readily biodegradable.
Bevorzugte pflanzliche Öle und Wachse als konditionierende Wirkstoffe sind Jojobaöl, Sonnenblumenöl. Orangenöl, Mandelöl, Weizenkeimöl und Pfirsichkernöl. Jojobaöl und Orangenöl sind besonders bevorzugt.Preferred vegetable oils and waxes as conditioning agents are jojoba oil, sunflower oil. Orange oil, almond oil, wheat germ oil and peach seed oil. Jojoba oil and orange oil are particularly preferred.
Insbesondere für die Formulierung sehr milder Zubereitungen hat es sich weiterhin als vorteilhaft erwiesen, wenn die Menge an gelösten anorganischen Salzen auf weniger als 2 Gew.-%, insbesondere weniger als 0,5 Gew.-% begrenzt wird. Dabei ist auch zu beachten, daß solche Salze nicht nur z.B. zur Einstellung der Viskosität zugegeben werden, sondern auch durch andere Wirkstoffe, insbesondere Tenside, eingebracht werden können.For the formulation of very mild preparations in particular, it has also proven to be advantageous if the amount of dissolved inorganic salts is limited to less than 2% by weight, in particular less than 0.5% by weight. It should also be noted that such salts are not only e.g. to adjust the viscosity, but can also be introduced by other active ingredients, in particular surfactants.
Weitere übliche Bestandteile für die erfindungsgemäßen Mittel sind: nichtionische Polymere wie beispielsweise Vinylpyrrolidon/Ninylacrylat-Copoly- mere, Polyvinylpyrrolidon und Vinylpyrrolidon/Vinylacetat-Copolymere, anionische Polymere, wie Polyacryl- und Polymethacrylsäuren, deren Salze, deren Copolymere mit Acrylsäure- und Methacrylsäureestern und -amiden und deren Derivate, die durch Kreuzvernetzung mit polyfunktionellen Agentien erhalten werden, Polyoxycarbonsäuren, wie Polyketo- und Polyaldehydocarbonsäuren und deren Salze, sowie Polymere und Copolymere der Crotonsäure mit Estern und Amiden der Acryl- und der Methacrylsäure, wie Vinylacetat-Crotonsäure- und Vinylacetat-Vinylpropio- nat-Crotonsäure-Copolymere, Strukturanten wie Glucose und Maleinsäure, haarkonditionierende Verbindungen wie Phospholipide, beispielsweise Sojalecithin, Ei-Lecithin und Kephaline, weitere Parfümöle, insbesondere solche mit der Duftnote einer Fracht, wie beispielsweise von Apfel, Bime. Erdbeere. Pfirsich, Aprikose. Ananas, Banane. Kirsche. Kiwi, Mango, Kokos. Mandel, Grapefruit. Maracuja, Mandarine und Melone, oder der Duftnote eines Genußmittels, wie beispielsweise von Tabak, Cola. Kaugummi, Guarana, Schokolade. Kakao, Vanille. Sarsaparilla, Pfefferminze und Rum. Dimethylisosorbid und Cyclodextrine,Other customary constituents for the agents according to the invention are: nonionic polymers such as vinylpyrrolidone / vinyl acrylate copolymers, polyvinylpyrrolidone and vinylpyrrolidone / vinyl acetate copolymers, anionic polymers such as polyacrylic and polymethacrylic acids, their salts, their copolymers with acrylic and methacrylic acid esters and - amides and their derivatives, which are obtained by crosslinking with polyfunctional agents, polyoxycarboxylic acids, such as polyketo and polyaldehydocarboxylic acids and their salts, and polymers and copolymers of crotonic acid with esters and amides of acrylic and methacrylic acid, such as vinyl acetate-crotonic acid and vinyl acetate. Vinyl propionate-crotonic acid copolymers, structurants such as glucose and maleic acid, hair-conditioning compounds such as phospholipids, for example soy lecithin, egg lecithin and cephalins, other perfume oils, in particular those with the fragrance note of a cargo, such as apple, bime. Strawberry. Peach apricot. Pineapple, banana. Cherry. Kiwi, mango, coconut. Almond, grapefruit. Passion fruit, tangerine and melon, or the scent of a luxury, such as tobacco, cola. Chewing gum, guarana, chocolate. Cocoa, vanilla. Sarsaparilla, peppermint and rum. Dimethyl isosorbide and cyclodextrins,
Lösungsvermittler, wie Ethanol, Isopropanol, Ethylenglykol, Propylenglykol, Glyce- rin, Diethylenglykol und ethoxylierte Triglyceride, Farbstoffe,Solubilizers, such as ethanol, isopropanol, ethylene glycol, propylene glycol, glycerin, diethylene glycol and ethoxylated triglycerides, dyes,
Antischuppenwirkstoffe wie Climbazol, Piroctone Olamine und Zink Omadine, Wirkstoffe wie Bisabolol, Allantoin, Panthenol, Niacinmid, Tocopherol und Pflanzenextrakte,Anti-dandruff agents such as climbazole, piroctone olamine and zinc omadine, active agents such as bisabolol, allantoin, panthenol, niacinmid, tocopherol and plant extracts,
Lichtschutzmittel,Light stabilizers,
Konsistenzgeber wie Zuckerester, Polyolester oder Polyolalkylether, Fette und Wachse, wie Walrat, Bienenwachs, Montanwachs, Paraffine, Ester, Glyce- ride und Fettalkohole, Fettsäurealkanolamide,Consistency enhancers such as sugar esters, polyol esters or polyol alkyl ethers, fats and waxes such as walrus, beeswax, montan wax, paraffins, esters, glycerides and fatty alcohols, fatty acid alkanolamides,
Komplexbildner wie EDTA, NTA, ß-Alanindiessigsäure und Phosphonsäuren, Quell- und Penetrationsstoffe wie PCA, Glycerin, Propylenglykolmonoethylether, Carbonate, Hydrogencarbonate, Guanidine, Harnstoffe sowie primäre, sekundäre und tertiäre Phosphate,Complexing agents such as EDTA, NTA, β-alaninediacetic acid and phosphonic acids, swelling and penetration substances such as PCA, glycerol, propylene glycol monoethyl ether, carbonates, hydrogen carbonates, guanidines, ureas and primary, secondary and tertiary phosphates,
Trübungsmittel wie Latex oder Styrol/Acrylamid-Copolymere, Perlglanzmittel wie Ethylenglykolmono- und -distearat oder PEG-3-distearat, direktziehende Farbstoffe sogenannte Kuppler- und Entwicklerkomponenten als Oxidationsfarbstoffvorpro- dukte,Opacifiers such as latex or styrene / acrylamide copolymers, pearlescent agents such as ethylene glycol mono- and distearate or PEG-3 distearate, direct dyes so-called coupler and developer components as oxidation dye precursors,
Reduktionsmittel wie z.B. Thioglykolsäure und deren Derivate, Thiomilchsäure, Cy- steamin, Thioäpfelsäure und α-Mercaptoethansulfonsäure, Oxidationsmittel wie Wasserstoffperoxid, Kaliumbromat und Natriumbromat, Treibmittel wie Propan-Butan-Gemische, N2O, Dimethylether, CO2 und Luft sowieReducing agents such as Thioglycolic acid and its derivatives, thiolactic acid, cytamine, thio malic acid and α-mercaptoethanesulfonic acid, oxidizing agents such as hydrogen peroxide, potassium bromate and sodium bromate, blowing agents such as propane-butane mixtures, N2O, dimethyl ether, CO2 and air and
Antioxidantien, Bitterstoffe, wie beispielsweise Denatonium Benzoate, Konservierungsmittel.Antioxidants, Bitter substances such as Denatonium Benzoate, preservatives.
Ebenfalls Gegenstand der Erfindung ist die Verwendung eines Mittels nach einem der Ansprüche 1 bis 10 zur Reinigung von Haut und Haaren.The invention also relates to the use of an agent according to one of claims 1 to 10 for cleaning skin and hair.
Die folgenden Beispiele sollen die Erfindung näher erläutern. The following examples are intended to explain the invention in more detail.
BeispieleExamples
Alle Mengenangaben sind, soweit nicht anders vermerkt, Gewichtsteile. 1. HaarshampoosUnless otherwise noted, all quantities are parts by weight. 1. Hair shampoos
Figure imgf000020_0001
Natriumlaurylethersulfat (ca. 70 % Aktivsubstanz in Wasser; INCI-Bezeichnung: Sodium Laureth Sulfat) (HENKEL)
Figure imgf000020_0001
Sodium lauryl ether sulfate (approx. 70% active substance in water; INCI name: Sodium Laureth sulfate) (HENKEL)
N,N-Dimethyl-N-kokosamidopropylammoniumacetobetain (ca. 30 % Aktivsubstanz in Wasser; INCI-Bezeichnung: Cocamidopropylbetain) (CLARIANT) N-Kokosfettsäureamidoethyl-N-2-hydroxyethylglycin-Natriumsalz (ca. 50 % Aktivsubstanz in Wasser; INCI-Bezeichnung: Disodium Cocoamphodiacetate) (WITCO) neutralisierter Ester von Alkylpolyglukose mit Weinsäure (ca. 30 % Aktivsubstanz in Wasser; ιNCI-Bezeichnung( vorläufig): Sodium Cocopolyglucose Tartrate) (CESALPINIA) neutralisierter Ester von Alkylpolyglukose mit Zitronensäure (ca. 30 % Aktivsubstanz in Wasser; ιNCI-Bezeichnung(vorläufig): Sodium Cocopolyglucose Citrate) (CESALPINIA)N, N-Dimethyl-N-coconut amidopropylammonium acetobetaine (approx. 30% active substance in water; INCI name: Cocamidopropyl betaine) (CLARIANT) N-coconut fatty acid amidoethyl-N-2-hydroxyethylglycine sodium salt (approx. 50% active substance in water; INCI name : Disodium Cocoamphodiacetate) (WITCO) neutralized ester of alkyl polyglucose with tartaric acid (approx. 30% active substance in water; ιNCI name (provisional): Sodium Cocopolyglucose Tartrate) (CESALPINIA) neutralized ester of alkyl polyglucose with citric acid (approx. 30% active substance in water ; ιNCI name (provisional): Sodium Cocopolyglucose Citrate) (CESALPINIA)
C8-14-Alkylpolyglucosid (ca. 52 % Aktivsubstanz in Wasser; INCI-Bezeichnung: Coco Glucoside) (HENKEL)C 8-14 alkyl polyglucoside (approx. 52% active substance in water; INCI name: Coco Glucoside) (HENKEL)
C12.14-Fettalkohol + 2,5 Ethylenoxid (INCI-Bezeichnung: Laureth-2) (HENKEL) Kokosmonoglycerid + 7,3 Ethylenoxid (INCI-Bezeichnung: PEG-7 Glyceryl Cocoate) (HENKEL)C 12 . 14 - fatty alcohol + 2.5 ethylene oxide (INCI name: Laureth-2) (HENKEL) coconut monoglyceride + 7.3 ethylene oxide (INCI name: PEG-7 glyceryl cocoate) (HENKEL)
D-Panthenylalkohol (75 % Aktivsubstanz in Wasser) (HOFFMANN LA-ROCHE) quaternierte Hydroxyethylcellulose (INCI-Bezeichnung: Polyquaternium- 10) (AMERCHOL)D-panthenyl alcohol (75% active substance in water) (HOFFMANN LA-ROCHE) quaternized hydroxyethyl cellulose (INCI name: Polyquaternium-10) (AMERCHOL)
Dimethyldiallylammoniumchlorid-Acrylamid-Copolymer (ca. 9 % Aktivsubstanz in Wasser; INCI-Bezeichnung: Polyquaternium-7) (MERCK)Dimethyldiallylammonium chloride-acrylamide copolymer (approx. 9% active substance in water; INCI name: Polyquaternium-7) (MERCK)
Terpolymer aus Acrylsäure, Methylacrylat und Methacrylamidopropyltrimomum- chlorid (INCI-Bezeichnung: Polyquaternium-47) (CALGON) Benzyldiethyl((2,6-xylylcarbamoyl)methyl)-ammoniumbenzoat (2,5 % Aktivsubstanz in Wasser; INCI-Bezeichnung: Aqua, Denatonium Benzoate) (MACFARLAN SMITH)Terpolymer of acrylic acid, methyl acrylate and methacrylamidopropyltrimomum chloride (INCI name: Polyquaternium-47) (CALGON) benzyldiethyl ((2,6-xylylcarbamoyl) methyl) ammonium benzoate (2.5% active substance in water; INCI name: Aqua, Denatonium Benzoate) (MACFARLAN SMITH)
Hydroxy-4-methyl-6(2,4,4-trimethylpentyl)-2-pyridon-Monoethanolamin-Salz (INCI-Bezeichnung: Piroctone Olamine) (CLARIANT)Hydroxy-4-methyl-6 (2,4,4-trimethylpentyl) -2-pyridone monoethanolamine salt (INCI name: Piroctone Olamine) (CLARIANT)
Weizenproteinhydrolysat (ca. 18 % Aktivsubstanz; INCI-Bezeichnung: Hydrolyzed Wheat Protein) (DGF STOESS) Silikon-Emulsion (INCI-Bezeichnung: Dimethiconol (and) TEA-Dodecylbenzene- sulfonate) (CALGON) Wheat protein hydrolyzate (approx. 18% active substance; INCI name: Hydrolyzed Wheat Protein) (DGF STOESS) Silicone emulsion (INCI name: Dimethiconol (and) TEA-Dodecylbenzenesulfonate) (CALGON)

Claims

Patentansprüche claims
1. Wäßriges kosmetisches Mittel zur Behandlung der Haare oder der Haut auf einer milden Tensidgrundlage, dadurch gekennzeichnet, daß es enthält: als Tensid mindestens einen Ester einer hydroxysubstituierten Bi- oder Tricar- bonsäure (A) mit der allgemeinen Formel (I),1. Aqueous cosmetic agent for the treatment of hair or skin on a mild surfactant base, characterized in that it contains: as surfactant at least one ester of a hydroxy-substituted bi- or tricarboxylic acid (A) with the general formula (I),
XX
II.
HO — C — COOR1 (I)HO - C - COOR 1 (I)
II.
Y — CH— COOR2 Y - CH - COOR 2
in derin the
X H oder eine -CH2COOR-Grappe ist,XH or a -CH 2 COOR group,
Y H oder -OH ist unter der Bedingung, daß Y H ist, wenn X -CH2COOR ist, R, R1 und R2 unabhängig voneinander ein Wasserstoffatom, ein Alkali- oder Erd-alkalimetallkation, eine Ammoniumgrappe, das Kation einer ammonium- organischen Base oder einen Rest Z, der von einer polyhydroxylierten organischen Verbindung stammt, die aus der Gruppe, die veretherte (C6-C18)-Alkyl- Polysaccharide mit 1 bis 6 monomeren Saccharideinheiten und veretherte ali- phatische (C6-C16)-Hydroxyalkyl-Polyole mit 2 bis 16 Hydroxylresten umfaßt, ausgewählt ist, bedeuten, unter der Bedingung, daß mindestens eine der Gruppen R, R1 oder R2 ein Rest Z ist, und mindestens ein Polymer (B), ausgewählt aus kationischen Polymeren und Ampho-Polymeren.YH or -OH is on the condition that Y is, when X is -CH 2 COOR, R, R 1 and R 2 independently of one another are a hydrogen atom, an alkali metal or alkaline earth metal cation, an ammonium group, the cation of an ammonium organic Base or a radical Z which is derived from a polyhydroxylated organic compound which is selected from the group consisting of etherified (C 6 -C 18 ) alkyl polysaccharides with 1 to 6 monomeric saccharide units and etherified aliphatic (C 6 -C 16 ) -Hydroxyalkyl polyols having 2 to 16 hydroxyl radicals, is selected, under the condition that at least one of the groups R, R 1 or R 2 is a radical Z, and at least one polymer (B) selected from cationic polymers and Ampho-polymers.
2. Mittel nach Anspruch 1, dadurch gekennzeichnet, daß der Rest Z der Verbindungen gemäß Formel (I) ein Polyglucose-(C6-C18)-monoalkylether mit 1 bis 6 Glukoseeinheiten ist.2. Composition according to claim 1, characterized in that the radical Z of the compounds of the formula (I) is a polyglucose (C 6 -C 18 ) monoalkyl ether having 1 to 6 glucose units.
3. Mittel nach Anspruch 1 oder 2, dadurch gekennzeichnet, daß die hydroxy-substi- tuierte Bi- oder Tricarbonsäure ausgewählt ist aus Weinsäure und Zitronensäure. 3. Composition according to claim 1 or 2, characterized in that the hydroxy-substituted bi- or tricarboxylic acid is selected from tartaric acid and citric acid.
4. Mittel nach einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, daß das Polymer (B) permanent kationisch ist.4. Composition according to one of claims 1 to 3, characterized in that the polymer (B) is permanently cationic.
5. Mittel nach Anspruch 4, dadurch gekennzeichnet, daß das Polymer (B) ausgewählt ist aus kationischen Cellulose-Derivaten.5. Composition according to claim 4, characterized in that the polymer (B) is selected from cationic cellulose derivatives.
6. Mittel nach einem der Ansprüche 1 bis 5, dadurch gekennzeichnet daß es sich um ein Haarreinigungsmittel, ein Duschbad, ein Schaumbad oder eine Flüssigseife handelt.6. Composition according to one of claims 1 to 5, characterized in that it is a hair cleaning agent, a shower bath, a foam bath or a liquid soap.
7. Mittel nach einem der Ansprüche 1 bis 6, dadurch gekennzeichnet, daß es mindestens ein weiteres Tensid enthält.7. Composition according to one of claims 1 to 6, characterized in that it contains at least one further surfactant.
8. Mittel nach Anspruch 7, dadurch gekennzeichnet, daß das weitere Tensid ausgewählt ist aus anionischen, zwitterionischen, amphoteren und nichtionogenen Tensiden.8. Composition according to claim 7, characterized in that the further surfactant is selected from anionic, zwitterionic, amphoteric and nonionic surfactants.
9. Mittel nach Ansprach 8, dadurch gekennzeichnet, das es ein zwitterionisches Tensid in Kombination mit einem anionischen und/oder einem nichtionogenen Tensid enthält.9. Composition according spoke 8, characterized in that it contains a zwitterionic surfactant in combination with an anionic and / or a nonionic surfactant.
10. Mittel nach einem der Ansprüche 1 bis 9, dadurch gekennzeichnet, daß es ein organisches Verdickungsmittel enthält.10. Composition according to one of claims 1 to 9, characterized in that it contains an organic thickener.
11. Verwendung eines Mittels nach einem der Ansprüche 1 bis 10 zur Reinigung von Haut oder Haaren. 11. Use of an agent according to any one of claims 1 to 10 for cleaning skin or hair.
PCT/EP2000/002969 1999-04-12 2000-04-04 Aqueous cosmetic preparations containing tartaric-acid or citric-acid esters of alkyl polyglucose and cationic or amphoteric polymers WO2000061101A1 (en)

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EP1762220A3 (en) * 2005-09-09 2010-06-09 Henkel AG & Co. KGaA Composition for dyeing keratinous fibres comprising polymers of low molecular weight

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WO2003059297A2 (en) * 2002-01-21 2003-07-24 Slovakofarma A.S. Dermatological topical compositions and a process for the preparation thereof
WO2003059297A3 (en) * 2002-01-21 2003-12-18 Slovakofarma As Dermatological topical compositions and a process for the preparation thereof
EP1762220A3 (en) * 2005-09-09 2010-06-09 Henkel AG & Co. KGaA Composition for dyeing keratinous fibres comprising polymers of low molecular weight

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