WO2003066017A1 - Washing preparations with vegetable oils - Google Patents

Washing preparations with vegetable oils Download PDF

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Publication number
WO2003066017A1
WO2003066017A1 PCT/EP2003/000908 EP0300908W WO03066017A1 WO 2003066017 A1 WO2003066017 A1 WO 2003066017A1 EP 0300908 W EP0300908 W EP 0300908W WO 03066017 A1 WO03066017 A1 WO 03066017A1
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Prior art keywords
oil
weight
acid
washing preparations
alkyl
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PCT/EP2003/000908
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German (de)
French (fr)
Inventor
Werner Seipel
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Cognis Deutschland Gmbh & Co. Kg
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Publication of WO2003066017A1 publication Critical patent/WO2003066017A1/en

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    • 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
    • A61K8/92Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof
    • A61K8/922Oils, fats or waxes; Derivatives thereof, e.g. hydrogenation products thereof of vegetable origin
    • 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
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • 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
    • A61K8/737Galactomannans, e.g. guar; Derivatives thereof
    • 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
    • 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

Definitions

  • the invention relates to cosmetic preparations containing vegetable oils from the field of washing products which contain selected surfactant mixtures, and to the use of the special surfactant mixtures for producing stable washing products containing vegetable oils.
  • European patent EP 0 744 936 B1 discloses skin and hair treatment compositions with alkylpolyglycosides, a polymer and a vegetable oil, which, particularly in the form of hair aftertreatment compositions, are intended to enable a combined use of various active ingredients which improve wet and dry combability and are effective against split ends and for a better one Color distribution of hair dyes lead. Up to 5% by weight of vegetable oils are processed in these formulations.
  • Wax-containing shampoos with small amounts of vegetable oils are also described in EP 0 505 616 AI.
  • the object of the present invention was to provide washing preparations with large amounts of vegetable oils which have good physical and chemical stability.
  • the preparations should be well tolerated, have a good washing effect, protect the skin and scalp from drying out and leave a pleasant feeling on the skin after use.
  • the invention relates to detergent-containing washing preparations containing at least 25% by weight of vegetable oils.
  • Another object of the invention is the use of surfactant mixtures containing alkyl and / or alkenyl oligoglycosides, amphoteric surfactants and optionally
  • the stable incorporation of large quantities of vegetable oil effectively reduces the drying out of the skin and scalp even with frequent washing and retains the moisture in the skin.
  • the washing preparations are characterized by good lipid-replenishing and moisturizing properties. Surprisingly, it was found that the preparations according to the invention have an excellent washing performance despite the high oil content, leave a pleasant feeling on the skin without a noticeable lubricating film and have good physical and chemical stability.
  • the combination of non-ionic and amphoteric surfactants enables physico-chemically stable incorporation of large quantities of vegetable oils. If cationic polymers are added to washing products for hair cosmetics, the conditioning effect, combability and manageability of the hair are improved even more sustainably.
  • Non-ionic, anionic, cationic and / or amphoteric or zwitterionic surfactants can be present as surface-active substances, the proportion of which in the detergents is usually about 10 to 90% by weight, preferably 20 to 70 and preferably 30 is up to 50% by weight.
  • anionic surfactants are soaps, alkyl benzene sulfonates, alkane sulfonates, olefin sulfonates, alkyl ether sulfonates,
  • Glycerol ether ⁇ -methyl ester sulfonates, sulfofatty acids, alkyl sulfates, fatty alcohol ether sulfates, Glycerol ether, Fettklareethersulfate, Hydroxymischethersul- sulfates, monoglyceride (ether) sulfates, fatty acid amide (ether) sulfates, mono- and dialkyl sulfosuccinates, mono- and dialkyl sulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid isethionates, fatty acid sarcosinates, fatty acid retaurides, N-acylamino acids, such as, for example, acyl lactylates, acyl tartrates, acyl glutamates and acyl aspartates, alkyl oligoglucoside sulfates
  • anionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution.
  • Typical examples of nonionic surfactants are fatty alcohol polyglycol ethers, alkyl phenol polyglycol ethers, fatty acid polyglycol esters, fatty acid amide polyglycol ethers, fatty amine polyglycol ethers, alkoxylated triglycerides, mixed ethers or mixed formals, optionally partially oxidized alk (en) yl oligoglycosides or alkyl glucoramide acid derivatives, in particular glucoronic acid protein derivatives, and glucoronic acid protein derivatives Wheat base), polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides.
  • nonionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution.
  • Typical examples of cationic surfactants are quaternary ammonium compounds and ester quats, in particular quaternized fatty acid trialkanolamine ester salts.
  • the vegetable oils used are - in contrast to volatile essential oils - fatty oils with a high proportion of di- and triglycerides.
  • Almond oil walnut oil, peach seed oil, avocado oil, soybean oil, sesame oil, sunflower seed oil,
  • Tsubaki oil evening primrose oil, rice bran oil, palm kernel oil, mangokem oil, cuckoo flower oil,
  • Safflower oil macadamia nut oil, grape seed oil, apricot kernel oil, babassu oil, olive oil,
  • Sasanqua oil, calendula oil, passion flower oil, Shorea Stenoptera butter and Shea butter are considered as vegetable oils.
  • Soybean oil almond oil, jojoba oil, olive oil, sunflower seed oil, sesame oil, evening primrose oil,
  • Thistle oil and wheat germ oil are preferred among them.
  • Soybean oil is particularly preferred.
  • At least 25% by weight, preferably at least 35% by weight and particularly preferably even at least 45% by weight of vegetable oils, based on the washing preparations, are used in the surfactant-containing washing preparations according to the invention.
  • Alkyl and alkenyl oligoglycosides are known nonionic surfactants which follow the formula (I)
  • R 1 is an alkyl and / or alkenyl radical having 4 to 22 carbon atoms
  • G is a sugar radical having 5 or 6 carbon atoms
  • p is a number from 1 to 10.
  • the alkyl and / or alkenyl oligoglycosides can be derived from aldoses or ketoses with 5 or 6 carbon atoms, preferably glucose.
  • the preferred alkyl and / or alkenyl oligoglycosides are thus alkyl and / or alkenyl oligoglucosides.
  • the index number p in the general formula (I) indicates the degree of oligomerization (DP), ie the distribution of mono- and oligoglycosides, and stands for a number between 1 and 10.
  • Alkyl and / or alkenyl oligoglycosides with an average degree of oligomerization p of 1.1 to 3.0 are preferably used. From an application point of view, preference is given to those alkyl and / or alkenyl oligoglycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.4.
  • the alkyl or alkenyl radical R 1 can be derived from primary alcohols having 4 to 11, preferably 8 to 10, carbon atoms. Typical examples are butanol, capronic alcohol, caprylic alcohol, capric alcohol and undecyl alcohol and their technical mixtures, such as are obtained, for example, in the hydrogenation of technical fatty acid methyl esters or in the course of the hydrogenation of aldehydes from Roelen's oxosynthesis.
  • the alkyl or alkenyl radical R 1 can also be derived from primary alcohols having 12 to 22, preferably 12 to 14, carbon atoms.
  • Typical examples are lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol, brassidyl alcohol and the technical mixtures described above, which can be obtained as well as their technical mixtures.
  • Alkyl oligoglucosides based on hardened C 2 -C 4 coco alcohol with a DP of 1 to 3 are preferred.
  • the alkyl oligoglucosides are used in amounts of 0.5 to 20% by weight, preferably 2.5 to 15 and particularly preferably 5 to 10% by weight, based on the washing preparation.
  • amphoteric - also listed under “zwitterionic surfactants” - are alkyl betaines, alkyl amido betaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines.
  • the surfactants mentioned are exclusively known compounds .Falbe (ed.), "Surfactants in Consumer Products", Springer Verlag, Berlin, 1987, pp. 54-124 or J.Falbe (ed.), "Catalysts, surfactants and mineral oil additives", Thieme Verlag, Stuttgart, 1978, Pp. 123-217.
  • Betaines are known surfactants which are predominantly produced by carboxyalkylation, preferably carboxymethylation, of aminic compounds.
  • the starting materials are preferably condensed with halocarboxylic acids or their salts, in particular with sodium chloroacetate, one mol of salt being formed per mole of betaine.
  • unsaturated carboxylic acids such as acrylic acid, is also possible.
  • betaines and "real" amphoteric surfactants reference is made to U.PIoog's contribution in Seifen- ⁇ le-Fette-Wwachs, 108, 373 (1982). Further overviews on this topic can be found for example by A. O'Lennick et al. in HAPPI, Nov.
  • betaines are the carboxyalkylation products of secondary and in particular tertiary amines which follow the formula (II) R 3
  • R 2 for alkyl and / or alkenyl radicals with 6 to 22 carbon atoms
  • R 3 for hydrogen or alkyl radicals with 1 to 4 carbon atoms
  • R 4 for alkyl radicals with 1 to 4 carbon atoms
  • n for numbers from 1 to 6
  • X for a Alkali and / or alkaline earth metal or ammonium.
  • Typical examples are the carboxymethylation products of hexylmethylamine, hexyldimethylamine, octyldimethylamine, De-cyldimethylamin, dodecylmethylamine, dodecyldimethylamine, Dodecylethylmethylamin, C i2 / ⁇ kyldimethylamin 4 -Kokosal-, myristyldimethylamine, cetyldimethylamine, stearyldimethylamine, Stearylethylmethyl-amine, oleyl dimethyl amine, C ⁇ 6 / i 8 - Tallow alkyl dimethylamine and their technical mixtures.
  • R 5 CO represents an aliphatic acyl radical having 6 to 22 carbon atoms and 0 or 1 to 3 double bonds
  • m represents numbers from 1 to 3 and R 3 , R 4 , n and X have the meanings given above.
  • Typical examples are reaction products of fatty acids with 6 to 22 carbon atoms, namely caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, araachearic acid , Gadoleic acid, behenic acid and erucic acid as well as their technical mixtures with N, N-dimethylaminoethylamine, N, N-dimethylaminopropylamine, N, N-diethylaminoethylamine and N, N-diethy
  • suitable starting materials for the betaines to be used in accordance with the invention are also imidazolines which follow the formula (IV) (IV)
  • R 6 is an alkyl radical having 5 to 21 carbon atoms
  • R 7 is a hydroxyl group
  • an OCOR 6 or NHCOR 7 radical and m is 2 or 3.
  • These substances are also known substances which can be obtained, for example, by the condensing condensation of 1 or 2 moles of fatty acid with polyhydric amines, such as, for example, aminoethylethanolamine (AEEA) or diethylenetriamine.
  • AEEA aminoethylethanolamine
  • diethylenetriamine diethylenetriamine
  • Typical examples are condensation products of the above-mentioned fatty acids with AEEA, preferably imidazolines based on lauric acid or again C 2 -C 4 coconut fatty acid, which are subsequently betainized with sodium chloroacetate.
  • the preferred amphoteric surfactants for the purposes of the present invention are betaines of the cocamidopropyl betaine type and sodium cocoamphoacetate.
  • the amphoteric surfactants are used in amounts of 0.5 to 30% by weight, preferably 2.5 to 20% by weight and particularly preferably 9 to 19% by weight, based on the washing preparations.
  • Suitable cationic polymers are, for example, cationic cellulose derivatives, such as, for example, a quaternized hydroxyethyl cellulose, which is available under the name Polymer JR 400® from Amerchol, cationic starch, copolymers of diallylammonium salts and acrylamides, quaternized vinyl-pyrrolidone / vinyl-imidazole polymers, such as, for example, luviquat ® (BASF), condensation products of polyglycols and amines, quaternized collagen polypeptides, such as, for example, lauryldimonium hydroxypropyl hydrolyzed collagen (Lamequat®L / Grünau), quaternized wheat polypeptides, polyethyleneimine, cationic silicone polymers, such as, for example, amidomethicones, copolymers of adipodinoxypropylene acid and dimethylaminohydroxyethylenediaminetroxyne diaminohydroxyethylene
  • copolymers of acrylic acid with dimethyldiallyl ammonium chloride (Merquat® 550 / Chemviron), polyaminopolyamides, as described for example in FR-A 2252840, and their crosslinked water-soluble polymers, cationic chitin derivatives, such as quaternized chit osan, optionally microcrystalline, condensation products from dihaloalkylene, such as dibromobutane with bisdialkylamines, such as bis-dimethylamino-1,3- propane, cationic guar gum, such as Jaguar® CBS, Jaguar® C-17, Jaguar® C-16 from Celanese, quaternized ammonium salt polymers, such as Mirapol® A-15, Mirapol® AD-1, Mirapol® AZ -1 from Miranol.
  • dihaloalkylene such as dibromobutane
  • bisdialkylamines such as bis-dimethylamino-1,3- propane
  • Cation polymers are used in the agents according to the invention in amounts of 0.02 to 5% by weight, preferably 0.05 to 3% by weight and particularly preferably in amounts of 0.1 to 2% by weight.
  • the average molecular weights of the cationic polymers should be between 5,000 and 1,000,000, preferably between 8,000 and 500,000 and particularly preferably between 10,000 and 400,000.
  • Cationic guar gum and / or quaternized ammonium salt polymers are particularly preferred as cation polymers.
  • Cation polymers are used in the washing preparations according to the invention in amounts of 0.1 to 5% by weight, preferably 0.5 to 4% by weight and particularly preferably 1 to 3% by weight, based on the washing preparations.
  • Predispersed wax dispersions can be used in the washing preparations in amounts of 0 to 5% by weight, preferably 0.005 to 3.5% by weight and particularly preferably in amounts of 0.01 to 3.1% by weight.
  • the proportion of the wax bodies contained in the wax dispersions is 10 to 40% by weight, preferably 15 to 35% by weight and particularly preferably 20 to 30% by weight, based on the predispersed wax dispersion.
  • Possible wax bodies in the wax dispersions are: alkylene glycol esters, fatty acid alkanolamides, partial glycerides, esters of polyvalent, optionally hydroxy-substituted carboxylic acids, fatty alcohols, fatty ketones, fatty aldehydes, fatty ethers, fatty carbonates, ring-opening products of olefin epoxides and mixtures thereof.
  • alkylene glycol esters which form the preferred wax bodies are usually mono- and / or diesters of alkylene glycols which follow the formula (V)
  • R 8 CO is a linear or branched, saturated or unsaturated acyl radical having 6 to 22 carbon atoms
  • R 9 is hydrogen or R 8 CO
  • A is a linear or branched alkylene radical having 2 to 4 carbon atoms and n is a number from 1 to 5 stands.
  • Typical examples are mono- and / or diesters of ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, triethylene glycol or tetraethylene glycol with fatty acids with 6 to 22, preferably 12 to 18 carbon atoms as there are: caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, linolenic acid Elaeostearic acid, arachic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures.
  • the use of ethylene glycol mono- and / or distearate is particularly preferred.
  • the water content of the formulations must be relatively low. Good physico-chemical stability of the washing preparations was achieved when the pure water content was at most 55% by weight, preferably at most 45% by weight and particularly preferably at most 35% by weight, based on the washing preparation.
  • the vegetable oil-containing washing preparations according to the invention are predominantly, but not exclusively, used in the field of cosmetic products.
  • washing preparations according to the invention preferably contain
  • the preparations according to the invention can serve as cosmetic and / or pharmaceutical preparations, such as, for example, hair shampoos, solid bars of soap, washing lotions, bubble baths, shower baths and preferably oil baths.
  • auxiliaries and additives they can also contain emulsifiers, further oil bodies, pearlescent waxes, consistency agents, superfatting agents, stabilizers, further polymers, silicone compounds, lecithins, phospholipids, biogenic active substances, antioxidants, antidandruff agents, film formers, hydrotropes, solubilizers, preservatives, perfume oils, dyes and dyes the like included.
  • suitable emulsifiers are, for example, nonionic substances from at least one of the following groups:
  • Partial esters of polyglycerin (average degree of self-condensation 2 to 8), polyethylene glycol (molecular weight 400 to 5000), trimethylolpropane, pentaerythritol, sugar alcohols (e.g. sorbitol), alkyl glucosides (e.g. methyl glucoside, butyl glucoside, lauryl glucoside) and polyglucosides saturated (e.g. cellulose) unsaturated, linear or branched fatty acids with 12 to 22 carbon atoms and / or hydroxycarboxylic acids with 3 to 18 carbon atoms and their adducts with 1 to 30 moles of ethylene oxide;
  • Block copolymers e.g. Polyethylene glycol 30 dipolyhydroxystearate;
  • the adducts of ethylene oxide and / or of propylene oxide with fatty alcohols, fatty acids, alkylphenols or with castor oil are known, commercially available products. These are mixtures of homologs whose average degree of alkoxylation is the ratio of the amounts of ethylene oxide and / or propylene oxide and Substrate with which the addition reaction is carried out corresponds.
  • C 12 ⁇ 8 - fatty acid monoesters and diesters of adducts of ethylene oxide with glycerol are known from DE 2024051 PS as refatting agents for cosmetic preparations.
  • Suitable partial glycerides are hydroxystearic acid monoglyceride, hydroxystearic acid diglyceride, isostearic acid monoglyceride,
  • Addition products of 1 to 30, preferably 5 to 10, mol of ethylene oxide onto the partial glycerides mentioned are also suitable.
  • sorbitan sorbitan As sorbitan sorbitan, sorbitan sesquiisostearate, sorbitan diisostearate, sorbitan triisostearate, sorbitan monooleate, sorbitan dioleate, trioleate, Sorbitanmonoerucat, Sorbitansesquierucat, Sorbitandierucat, Sorbitantrierucat, Sorbitanmonoricinoleat, Sorbitansesquiricinoleat, Sorbitandiricinoleat, Sorbitantriricinoleat, Sorbitanmonohydroxystearat, sorbitan come sesquihydroxystearat, Sorbitandihydroxystearat, Sorbitantrihydroxystearat,
  • Addition products of 1 to 30, preferably 5 to 10, mol of ethylene oxide onto the sorbitan esters mentioned are also suitable. > Polyglycerol esters
  • polyglycerol esters are polyglyceryl-2 dipolyhydroxystearate (Dehymuls® PGPH), polyglycerol-3-diisostearate (Lameform® TGI), polyglyceryl-4 isostearate (Isolan® GI 34), polyglyceryl-3 oleate, diisostearoyl polyglyearyl-3 diisostearate ® PDI), Polyglyceryl-3 Methylglucose Distearate (Tego Care® 450), Polyglyceryl-3 Beeswax (Cera Bellina®), Polyglyceryl-4 Caprate (Polyglycerol Caprate T2010 / 90), Polyglyceryl-3 Cetyl Ether (Chimexane® NL), Polyglyceryl -3 Distearate (Cremophor® GS 32) and Polyglyceryl Polyricinoleate (Admul® WOL 1403) Polyglyceryl Dimerate Is
  • polystyrene resin examples include the mono-, di- and triesters of trimethylolpropane or pentaerythritol with lauric acid, coconut fatty acid, taig fatty acid, palmitic acid, stearic acid, oleic acid, behenic acid and the like which are optionally reacted with 1 to 30 mol of ethylene oxide.
  • Typical anionic emulsifiers are aliphatic fatty acids with 12 to 22 carbon atoms, such as, for example, palmitic acid, stearic acid or behenic acid, and dicarboxylic acids with 12 to 22 carbon atoms, such as, for example, azelaic acid or sebacic acid.
  • Washing preparations also use smaller amounts of other oil bodies, such as Guerbet alcohols based on fatty alcohols having 6 to 18, preferably 8 to 10 carbon atoms, esters of linear C 6 -C 22 fatty acids with linear or branched C 6 -C 22 fatty alcohols or Esters of branched C 6 -C 3 carboxylic acids with linear or branched C 6 -C 22 fatty alcohols, such as myristyl myristate, myristyl palmitate,
  • other oil bodies such as Guerbet alcohols based on fatty alcohols having 6 to 18, preferably 8 to 10 carbon atoms, esters of linear C 6 -C 22 fatty acids with linear or branched C 6 -C 22 fatty alcohols or Esters of branched C 6 -C 3 carboxylic acids with linear or branched C 6 -C 22 fatty alcohols, such as myristyl myristate, myristyl palmitate,
  • esters of linear C 6 -C 22 fatty acids with branched alcohols in particular 2-ethylhexanol
  • esters of C 8 -C 38 alkylhydroxycarboxylic acids with linear or branched C 6 -C 22 fatty alcohols cf.
  • dioctyl malates esters of linear and / or branched fatty acids with polyhydric alcohols (such as propylene glycol, dimer diol or trimer triol) and / or Guerbet alcohols, triglycerides based on C 6 -C0 0 fatty acids, liquid mono7 di / triglyceride mixtures based on C 6 -C 8 fatty acids, esters of C 6 -C 22 fatty alcohols and / or Guerbet alcohols with aromatic carboxylic acids, in particular benzoic acid, esters of C 2 -C 2 dicarboxylic acids with linear or branched alcohols having 1 to 22 carbon atoms or polyols 2 to 10 carbon atoms and 2 to 6 hydroxyl groups, branched primary alcohols, substituted cyclohexanes, linear and branched C 6 -C 22 fatty alcohol carbonates, such as, for example, dicaprylyl car bonate (C
  • Finsolv® TN linear or branched , symmetrical or asymmetrical dialkyl ethers with 6 to 22 carbon atoms per alkyl group, such as dicaprylyl ether (Cetiol® OE), ring opening products of epoxidized fatty acid esters with polyols, silicone oils (cyclomethicones, silicon methicone types etc.) and / or aliphatic or naphthenic hydrocarbons, such as squalane , Squalene or dialkylcyclohexanes.
  • dicaprylyl ether such as dicaprylyl ether (Cetiol® OE)
  • silicone oils cyclomethicones, silicon methicone types etc.
  • aliphatic or naphthenic hydrocarbons such as squalane , Squalene or dialkylcyclohexanes.
  • Pearlescent waxes that can be used are, for example: alkylene glycol esters, especially ethylene glycol distearate; Fatty acid alkanolamides, especially coconut fatty acid diethanolamide; Partial glycerides, especially stearic acid monoglyceride; Esters of polyvalent, optionally hydroxy-substituted carboxylic acids with fatty alcohols having 6 to 22 carbon atoms, especially long-chain esters of tartaric acid; Fatty substances, such as, for example, fatty alcohols, fatty ketones, fatty aldehydes, fatty ethers and fatty carbonates, which have a total of at least 24 carbon atoms, especially lauron and distearyl ether; Fatty acids such as stearic acid, hydroxystearic acid or behenic acid, ring opening products of olefin epoxides with 12 to 22 carbon atoms with fatty alcohols. Consistency agents and thickeners
  • Suitable consistency agents are primarily fatty alcohols or hydroxy fatty alcohols with 12 to 22 and preferably 16 to 18 carbon atoms and, in addition, partial glycerides, fatty acids or hydroxy fatty acids.
  • a combination of these substances with alkyl oligoglucosides and / or fatty acid N-methylglucamides of the same chain length and / or polyglycerol poly-12-hydroxystearates is preferred.
  • Suitable thickeners are, for example, Aerosil types (hydrophilic silicas), polysaccharides, in particular xanthan gum, agar agar, alginates and tyloses, carboxymethyl cellulose and hydroxyethyl and hydroxypropyl cellulose, and also higher molecular weight polyethylene glycol mono- and diesters of fatty acids, polyacrylates (e.g. Carbopole® and Pemulen types from Goodrich; Synthalene® from Sigma; Keltrol types from Kelco; Sepigel types from Seppic; Salcare types from Allied Colloids), polyacrylamides, polymers, polyvinyl alcohol and polyvinylpyrrolidone. Bentonites, such as e.g.
  • Bentone® Gel VS-5PC which is a mixture of cyclopentasiloxane, disteardimonium hectorite and propylene carbonate.
  • Surfactants such as ethoxylated fatty acid glycerides, esters of fatty acids with polyols such as pentaerythritol or trimethylolpropane, fatty alcohol ethoxylates with a narrow homolog distribution or alkyl oligoglucosides as well as electrolytes such as table salt and ammonium chloride are also suitable.
  • Substances such as, for example, lanolin and lecithin and polyethoxylated or acylated lanolin and lecithin derivatives, polyol fatty acid esters, monoglycerides and fatty acid alkanolamides can be used as superfatting agents, the latter simultaneously serving as foam stabilizers.
  • Metal salts of fatty acids such as magnesium, aluminum and / or zinc stearate or ricinoleate can be used as stabilizers.
  • the preferred polymers are the cation polymers already described. However, other polymers can also be used.
  • Anionic, zwitterionic, amphoteric and nonionic polymers are, for example, vinyl acetate / crotonic acid copolymers, vinylpyrrolidone / vinyl acrylate copolymers, vinyl acetate / butyl maleate / isobornyl acrylate copolymers,
  • Hydroxypropyl methacrylate copolymers polyvinylpyrrolidone, vinylpyrrolidone / vinyl acetate copolymers, vinylpyrrolidone / dimethylaminoethyl methacrylate / vinylcaprolactam terpolymers and, if appropriate, derivatized cellulose ethers and silicones.
  • Other suitable polymers and thickeners are in Cosm.Toil. 108, 95 (1993).
  • Suitable silicone compounds are, for example, dimethylpolysiloxanes, methylphenylpolysiloxanes, cyclic silicones and amino, fatty acid, alcohol, polyether, epoxy, fluorine, glycoside and / or alkyl-modified silicone compounds, which can be both liquid and resinous at room temperature.
  • Simethicones which are mixtures of dimethicones with an average chain length of 200 to 300 dimethylsiloxane units and hydrogenated silicates, are also suitable.
  • a detailed overview of suitable volatile silicones can also be found by Todd et al. in Cosm.Toil. 91, 27 (1976).
  • biogenic active substances include tocopherol, tocopherol acetate, tocopherol palmitate, ascorbic acid, (deoxy) ribonucleic acid and its fragmentation products, ß-glucans, retinol, bisabolol, allantoin, phytantriol, panthenol, AHA acids, amino acids, ceramides, pseudocleamides, extracts of essential oils, essential extracts such as Prunus extract, Bambaranus extract and vitamin complexes. film formers
  • Common film formers are, for example, chitosan, microcrystalline chitosan, quaternized chitosan, polyvinylpyrrolidone, vinylpyrrolidone-vinyl acetate copolymers, polymers of the acrylic acid series, quaternary cellulose derivatives, collagen, hyaluronic acid or its salts and similar compounds.
  • Piroctone olamine (1-hydroxy-4-methyl-6- (2,4,4-trimythylpentyl) -2- (1H) -pyridinone monoethanolamine salt
  • Baypival® (climbazole), Ketoconazol®, (4-acetyl-l - ⁇ - 4- [2- (2.4-dichlorophenyl) r-2- (lH-imidazol-l-ylmethyl) -l, 3-dioxylan-c-4-ylmethoxyphenyl ⁇ piperazine, ketoconazole, elubiol, selenium disulfide, sulfur colloidal, Schwefelpolyehtylenglykolsorbitanmonooleat, Schwefelrizinolpolyehtoxylat, Schwfel tar distillate, salicylic acid (or in combination with hexachlorophene), Undexy- lensäure monoethanolamide sulfosuccinate Na salt, Lamepon® UD (protein unde
  • Hydrotropes such as ethanol, isopropyl alcohol or polyols can also be used to improve the flow behavior.
  • Polyols that come into consideration here preferably have 2 to 15 carbon atoms and at least two hydroxyl groups.
  • the polyols can also contain further functional groups, in particular amino groups, or be modified with nitrogen. Typical examples are
  • Alkylene glycols such as ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, hexylene glycol and polyethylene glycols with an average molecular weight of 100 to 1,000 daltons;
  • Methyl compounds such as in particular trimethylolethane, trimethylolpropane, trimethylolbutane, pentaerythritol and dipentaerythritol;
  • Dialcohol amines such as diethanolamine or 2-amino-l, 3-propanediol.
  • Suitable preservatives are, for example, phenoxyethanol, formaldehyde solution, parabens, pentanediol or sorbic acid, as well as the silver complexes known under the name Surfacine® and the other classes of substances listed in Appendix 6, Parts A and B of the Cosmetics Ordinance.
  • Perfume oils include mixtures of natural and synthetic fragrances. Natural fragrances are extracts of flowers (lily, lavender, roses, jasmine, neroli, ylang-ylang), stems and leaves (geranium, patchouli, petitgrain), fruits (anise, coriander, caraway, juniper), fruit peel (bergamot, lemon, Oranges), roots (mace, angelica, celery, cardamom, costus, iris, calmus), wood (pine, sandal, guaiac, cedar, rosewood), herbs and grasses (tarragon, lemongrass, sage, thyme), Needles and twigs (spruce, fir, pine, mountain pine), resins and balms (galbanum, elemi, benzoin, myrrh, olibanum, opoponax).
  • Typical synthetic fragrance compounds are products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type. Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinylacetate, phenylethyl acetate, linalyl benzoate, benzyl formate, ethyl methylphenyl glycinate, allyl cyclohexyl benzylatepylpropionate, stally.
  • the ethers include, for example, benzyl ethyl ether, the aldehydes, for example, the linear alkanals having 8 to 18 carbon atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamenaldehyde, hydroxycitronellal, lilial and bourgeonal, the ketones, for example, the jonones, ⁇ -isomethylionone and methylcedryl ketone, the alcohols Anethol, citronellol, eugenol, isoeugenol, geraniol, linalool, phenylethyl alcohol and terpineol, the hydrocarbons mainly include the terpenes and balsams.
  • the aldehydes for example, the linear alkanals having 8 to 18 carbon atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamenalde
  • fragrance oils which together produce an appealing fragrance.
  • essential oils of lower volatility most of the time are used as aroma components, are suitable as perfume oils, for example sage oil, chamomile oil, clove oil, lemon balm oil, mint oil, cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, oliban oil, galbanum oil, labolanum oil and lavandin oil.
  • Suitable flavors are, for example, peppermint oil, spearmint oil, anise oil, star anise oil, caraway oil, eucalyptus oil, fennel oil, lemon oil, wintergreen oil, clove oil, menthol and the like.
  • the dyes which can be used are those substances which are suitable and approved for cosmetic purposes, as compiled, for example, in the publication "Cosmetic Dyes” by the Dye Commission of the German Research Foundation, Verlag Chemie, Weinheim, 1984, pp. 81-106. Examples are culinary red A (CI 16255), patent blue V (CI42051), indigotine (CI73015), chlorophyllin (CI75810), quinoline yellow (CI47005), titanium dioxide (CI77891), indanthrene blue RS (CI 69800) and madder varnish (CI58000). Luminol may also be present as the luminescent dye. These dyes are usually used in concentrations of 0.001 to 0.1% by weight, based on the mixture as a whole.
  • the production takes place at room temperature. All substances are mixed together homogeneously.

Abstract

The invention relates to surfactant-containing washing preparations with at least 25 percent by weight of a vegetable oil and to the utilization of mixtures containing alkyl and/or alkenyl oligoglycosides, amphoteric surfactant and optionally cationic polymers for the production of washing preparations with at least 25 percent by weight of vegetable oils. Said washing preparations are characterized by good enriching and moisturizing properties, high physico-chemical stability and a pleasant skin feeling after application.

Description

Waschzubereitungen mit PflanzenölenWashing preparations with vegetable oils
Gebiet der ErfindungField of the Invention
Die Erfindung betrifft pflanzenölhaltige kosmetische Zubereitungen aus dem Bereich der Waschprodukte, die ausgewählte Tensidmischungen enthalten, sowie die Verwendung der speziellen Tensidmischungen zur Herstellung stabiler pflanzenölhaltiger Waschprodukte.The invention relates to cosmetic preparations containing vegetable oils from the field of washing products which contain selected surfactant mixtures, and to the use of the special surfactant mixtures for producing stable washing products containing vegetable oils.
Stand der TechnikState of the art
Unbeachtet der Tatsache, dass häufiges Waschen Haut und Haaren den natürlichen, schützenden Fettfilm entzieht, zu einer verstärkten Austrocknung führt und Haut und Haare damit durch äußere Einflüsse angreifbar macht, entsprechen häufige Wäschen dennoch dem heutigen Reinheitsideal.Despite the fact that frequent washing deprives skin and hair of the natural, protective grease film, leads to increased dehydration and thus makes skin and hair vulnerable to external influences, frequent washes still correspond to today's ideal of cleanliness.
Der Anfälligkeit gegen schädigende Umwelteinflüsse entgegen zu wirken, versucht die Kosmetikindustrie mit verschiedensten Hilfs- und Zusatzstoffen in Waschpräparaten die verstärkte Austrocknungsgefahr zu reduzieren. Es werden dabei zwei Prinzipien verfolgt. Einerseits soll durch Zugabe von hygroskopischen Stoffen, die sich im Stratum corneum einlagern und Wasser binden, die Feuchtigkeit der Haut gehalten werden. Die Bindekapazität des Stratum corneums bezüglich dieser Substanzen während des Wasch prozesses muß jedoch kritisch hinterfragt werden. Andererseits wird über eine Okklusion der Haut durch lipophile Grundlagen das körpereigene Wasser länger in der Haut festgehalten. Besonders gut verträgliche und bioabbaubare lipophile Grundlagen sind Öle pflanzlichen Ursprungs.To counteract the susceptibility to damaging environmental influences, the cosmetics industry tries to reduce the increased risk of dehydration with a wide variety of auxiliaries and additives in washing preparations. Two principles are followed. On the one hand, the addition of hygroscopic substances that are stored in the stratum corneum and bind water should keep the moisture in the skin. The binding capacity of the stratum corneum with regard to these substances during the washing process must, however, be critically examined. On the other hand, through an occlusion of the skin through lipophilic bases, the body's own water is held longer in the skin. Oils of vegetable origin are particularly well tolerated and biodegradable lipophilic bases.
Größere Mengen Pflanzenöle führen jedoch häufig zu einer Instabilität der Waschformulierungen, zu einer Verminderung der Waschkapazität oder zu einem unangenehmen Hautgefühl nach der Anwendung.However, larger amounts of vegetable oils often lead to instability in the washing formulations, to a reduction in the washing capacity or to an uncomfortable feeling on the skin after use.
In der Europäischen Patentschrift EP 0 744 936 Bl werden Haut- und Haarbehandlungsmittel mit Alkylpolyglycosiden, einem Polymeren und einem Pflanzenöl offenbart, die besonders in Form von Haarnachbehandlungsmitteln eine kombinierte Anwendung verschiedener Wirkstoffe ermöglichen sollen, die die Naß- und Trockenkämmbarkeit verbessern, gegen Spliß wirksam sind und zu einer besseren Farbverteilung von Haarfärbemitteln führen. In diesen Formulierungen werden bis zu 5 Gew. % Pflanzenöle verarbeitet.European patent EP 0 744 936 B1 discloses skin and hair treatment compositions with alkylpolyglycosides, a polymer and a vegetable oil, which, particularly in the form of hair aftertreatment compositions, are intended to enable a combined use of various active ingredients which improve wet and dry combability and are effective against split ends and for a better one Color distribution of hair dyes lead. Up to 5% by weight of vegetable oils are processed in these formulations.
Wachshaltige Haarwaschmittel mit geringen Mengen pflanzlicher Öle werden auch in der EP 0 505 616 AI beschrieben.Wax-containing shampoos with small amounts of vegetable oils are also described in EP 0 505 616 AI.
Die Aufgabe der vorliegenden Erfindung hat darin bestanden, Waschzubereitungen mit großen Mengen an pflanzlichen Ölen zur Verfügung zu stellen, die eine gute physikalische und chemische Stabilität aufweisen. Die Zubereitungen sollen gut verträglich sein, einen guten Wascheffekt aufweisen, die Haut und Kopfhaut vor Austrocknung schützen und nach der Anwendung ein angenehmes Hautgefühl hinterlassen.The object of the present invention was to provide washing preparations with large amounts of vegetable oils which have good physical and chemical stability. The preparations should be well tolerated, have a good washing effect, protect the skin and scalp from drying out and leave a pleasant feeling on the skin after use.
Beschreibung der ErfindungDescription of the invention
Gegenstand der Erfindung sind tensidhaltige Waschzubereitungen, enthaltend mindestens 25 Gew. % Pflanzenöle.The invention relates to detergent-containing washing preparations containing at least 25% by weight of vegetable oils.
Ein weiterer Gegenstand der Erfindung ist die Verwendung von Tensidmischungen, enthaltend Alkyl- und/oder Alkenyloligoglykoside, amphotere Tenside und gegebenenfallsAnother object of the invention is the use of surfactant mixtures containing alkyl and / or alkenyl oligoglycosides, amphoteric surfactants and optionally
Kationpolymere zur Herstellung von Waschzubereitungen mit mindestens 25 Gew.%Cation polymers for the production of washing preparations with at least 25% by weight
Pflanzenöl.Vegetable oil.
Durch die stabile Einarbeitung großer Mengen Pflanzenöl wird die Austrocknung von Haut und Kopfhaut auch bei häufigem Waschen effektiv vermindert und die Feuchtigkeit in der Haut zurückgehalten. Die Waschzubereitungen zeichnen sich durch gute rückfettende und feuchthaltende Eigenschaften aus. Überraschenderweise wurde gefunden, daß die erfindungsgemäßen Zubereitungen trotz des hohen Ölanteils eine hervorragende Waschleistung haben, nach der Anwendung ein angenehmes Hautgefühl ohne spürbaren Schmierfilm hinterlassen und eine gute physikalische und chemische Stabilität aufweisen. Die Kombination aus nichtionischen und amphoteren Tensiden ermöglicht dabei die physico-chemisch stabile Einarbeitung großer Mengen Pflanzenöle. Setzt man weiterhin bei Waschprodukten für die haarkosmetische Anwendung kationische Polymere zu, wird der konditionierende Effekt, die Kämmbarkeit und Frisierbarkeit des Haares noch nachhaltiger verbessert.The stable incorporation of large quantities of vegetable oil effectively reduces the drying out of the skin and scalp even with frequent washing and retains the moisture in the skin. The washing preparations are characterized by good lipid-replenishing and moisturizing properties. Surprisingly, it was found that the preparations according to the invention have an excellent washing performance despite the high oil content, leave a pleasant feeling on the skin without a noticeable lubricating film and have good physical and chemical stability. The combination of non-ionic and amphoteric surfactants enables physico-chemically stable incorporation of large quantities of vegetable oils. If cationic polymers are added to washing products for hair cosmetics, the conditioning effect, combability and manageability of the hair are improved even more sustainably.
Tensidesurfactants
Als oberflächenaktive Stoffe können nichtionische, anionische, kationische und/oder amphotere bzw. zwitterionische Tenside enthalten sein, deren Anteil an den Mitteln üblicherweise bei etwa 10 bis 90 Gew. %, vorzugsweise 20 bis 70 und vorzugsweise 30 bis 50 Gew.-% beträgt. Typische Beispiele für anionische Tenside sind Seifen, Alkylbenzolsulfonate, Alkansulfonate, Olefinsulfonate, Alkylethersulfonate,Non-ionic, anionic, cationic and / or amphoteric or zwitterionic surfactants can be present as surface-active substances, the proportion of which in the detergents is usually about 10 to 90% by weight, preferably 20 to 70 and preferably 30 is up to 50% by weight. Typical examples of anionic surfactants are soaps, alkyl benzene sulfonates, alkane sulfonates, olefin sulfonates, alkyl ether sulfonates,
Glycerinethersulfonate, α-Methylestersulfonate, Sulfofettsäuren, Alkylsulfate, Fettalkoholethersulfate, Glycerinethersulfate, Fettsäureethersulfate, Hydroxymischethersul- fate, Monoglycerid(ether)sulfate, Fettsäureamid(ether)-sulfate, Mono- und Dialkyl- sulfosuccinate, Mono- und Dialkylsulfosuccinamate, Sulfotriglyceride, Amidseifen, Ethercarbonsäuren und deren Salze, Fettsäureisethionate, Fettsäuresarcosinate, Fettsäu- retauride, N-Acylaminosäuren, wie beispielsweise Acyllactylate, Acyltartrate, Acylglutamate und Acyl-aspartate, Alkyloligoglucosidsulfate, Proteinfettsäurekondensate (insbesondere pflanzliche Produkte auf Weizenbasis) und Alkyl(ether)phosphate. Sofern die anionischen Tenside Polyglycoletherketten enthalten, können diese eine konventionelle, vorzugsweise jedoch eine eingeengte Homologenverteilung aufweisen. Typische Beispiele für nichtionische Tenside sind Fettalkoholpolyglycolether, Alkyl-phenolpolyglycolether, Fettsäurepolyglycolester, Fettsäureamidpolyglycolether, Fettaminpolyglycolether, alkoxylierte Triglyceride, Mischether bzw. Mischformale, gegebenenfalls partiell oxidierte Alk(en)yloligoglykoside bzw. Glucoronsäurederivate, Fettsäure-N-alkylglucamide, Proteinhydrolysate (insbesondere pflanzliche Produkte auf Weizenbasis), Polyolfett- säureester, Zuckerester, Sorbitanester, Polysorbate und Aminoxide. Sofern die nichtionischen Tenside Polyglycoletherketten enthalten, können diese eine konventionelle, vorzugsweise jedoch eine eingeengte Homologenverteilung aufweisen. Typische Beispiele für kationische Tenside sind quartäre Ammoniumverbindungen und Esterquats, insbesondere quaternierte Fettsäuretrialkanolaminestersalze.Glycerol ether, α-methyl ester sulfonates, sulfofatty acids, alkyl sulfates, fatty alcohol ether sulfates, Glycerol ether, Fettsäureethersulfate, Hydroxymischethersul- sulfates, monoglyceride (ether) sulfates, fatty acid amide (ether) sulfates, mono- and dialkyl sulfosuccinates, mono- and dialkyl sulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid isethionates, fatty acid sarcosinates, fatty acid retaurides, N-acylamino acids, such as, for example, acyl lactylates, acyl tartrates, acyl glutamates and acyl aspartates, alkyl oligoglucoside sulfates, protein fatty acid condensates (in particular vegetable products based on wheat) and alkyl (ether) phosphates. If the anionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution. Typical examples of nonionic surfactants are fatty alcohol polyglycol ethers, alkyl phenol polyglycol ethers, fatty acid polyglycol esters, fatty acid amide polyglycol ethers, fatty amine polyglycol ethers, alkoxylated triglycerides, mixed ethers or mixed formals, optionally partially oxidized alk (en) yl oligoglycosides or alkyl glucoramide acid derivatives, in particular glucoronic acid protein derivatives, and glucoronic acid protein derivatives Wheat base), polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides. If the nonionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution. Typical examples of cationic surfactants are quaternary ammonium compounds and ester quats, in particular quaternized fatty acid trialkanolamine ester salts.
Pflanzenölevegetable oils
Unter den eingesetzten Pflanzenölen werden - im Unterschied zu leicht flüchtigen ätherischen Ölen - fette Öle mit hohem Anteil an Di- und Triglyceriden verstanden.The vegetable oils used are - in contrast to volatile essential oils - fatty oils with a high proportion of di- and triglycerides.
Als beispiele kommen die größtenteils in der EP 0 744 936 Bl erwähnten PflanzenöleThe vegetable oils mostly mentioned in EP 0 744 936 B1 come as examples
Mandelöl, Walnußöl, Pfirsichkemöl, Avocadoöl, Sojaöl, Sesamöl, Sonnenblumenkernöl,Almond oil, walnut oil, peach seed oil, avocado oil, soybean oil, sesame oil, sunflower seed oil,
Tsubakiöl, Nachtkerzenöl, Reiskleieöl, Palmkemöl, Mangokemöl, Wiesenschaumkrautöl,Tsubaki oil, evening primrose oil, rice bran oil, palm kernel oil, mangokem oil, cuckoo flower oil,
Distelöl, Macadamianußsöl, Traubenkernöl, Aprikosenkernöl, Babassuöl, Olivenöl,Safflower oil, macadamia nut oil, grape seed oil, apricot kernel oil, babassu oil, olive oil,
Weizenkeimöl, Kürbiskernöl, Malvenöl, Haselnußsöl, Safloröl, Jojobaöl, Canolaöl,Wheat germ oil, pumpkin seed oil, mallow oil, hazelnut oil, safflower oil, jojoba oil, canola oil,
Sasanqua-Öl, Calendulaöl, Passionsblumenöl, Shorea Stenoptera Butter und Shea- Butter als pflanzliche Öle in Betracht.Sasanqua oil, calendula oil, passion flower oil, Shorea Stenoptera butter and Shea butter are considered as vegetable oils.
Sojaöl, Mandelöl, Jojobaöl, Olivenöl, Sonnenblumenkernöl, Sesamöl, Nachtkerzenöl,Soybean oil, almond oil, jojoba oil, olive oil, sunflower seed oil, sesame oil, evening primrose oil,
Distelöl und Weizenkeimöl werden darunter bevorzugt. Besonders bevorzugt ist Sojaöl. In den erfindungsgemäßen tensidhaltigen Waschzubereitungen werden mindestens 25 Gew.%, vorzugsweise mindestens 35 Gew.% und besonders bevorzugt sogar mindestens 45 Gew.% Pflanzenöle - bezogen auf die Waschzubereitungen eingesetzt.Thistle oil and wheat germ oil are preferred among them. Soybean oil is particularly preferred. At least 25% by weight, preferably at least 35% by weight and particularly preferably even at least 45% by weight of vegetable oils, based on the washing preparations, are used in the surfactant-containing washing preparations according to the invention.
Alkyl- und/oder AlkenyloligoqlykosideAlkyl and / or alkenyl oligoglycosides
Alkyl- und Alkenyloligoglykoside stellen bekannte nichtionische Tenside dar, die der Formel (I) folgen,Alkyl and alkenyl oligoglycosides are known nonionic surfactants which follow the formula (I)
Figure imgf000005_0001
Figure imgf000005_0001
in der R1 für einen Alkyl- und/oder Alkenylrest mit 4 bis 22 Kohlenstoffatomen, G für einen Zuckerrest mit 5 oder 6 Kohlenstoffatomen und p für Zahlen von 1 bis 10 steht. Sie können nach den einschlä-gigen Verfahren der präparativen organischen Chemie erhalten werden. Stellvertretend für das umfangreiche Schrifttum sei hier auf die Übersichtsarbeit von Biermann et al. in Starch/Stärke 45, 281 (1993), B.Salka in Cosm.Toil. 108, 89 (1993) sowie J.Kahre et al. in SÖFW-Journal Heft 8, 598 (1995) ver wiesen.in which R 1 is an alkyl and / or alkenyl radical having 4 to 22 carbon atoms, G is a sugar radical having 5 or 6 carbon atoms and p is a number from 1 to 10. They can be obtained according to the relevant preparative organic chemistry methods. Representative of the extensive literature here is the review by Biermann et al. in Starch /force 45, 281 (1993), B.Salka in Cosm.Toil. 108, 89 (1993) and J.Kahre et al. in SÖFW-Journal Issue 8, 598 (1995).
Die Alkyl- und/oder Alkenyloligoglykoside können sich von Aldosen bzw. Ketosen mit 5 oder 6 Kohlen-stoffatomen, vorzugsweise der Glucose ableiten. Die bevorzugten Alkyl- und/oder Alkenyloligoglykoside sind somit Alkyl- und/oder Alkenyloligoglucoside. Die Indexzahl p in der allgemeinen Formel (I) gibt den Oligomerisierungsgrad (DP), d. h. die Verteilung von Mono- und Oligoglykosiden an und steht für eine Zahl zwischen 1 und 10. Während p in einer gegebenen Verbindung stets ganzzahlig sein muß und hier vor allem die Werte p = 1 bis 6 annehmen kann, ist der Wert p für ein bestimmtes Alkyloligo- glykosid eine analytisch ermittelte rechnerische Größe, die meistens eine gebrochene Zahl darstellt. Vorzugsweise werden Alkyl- und/oder Alkenyloligoglykoside mit einem mittleren Oligomerisierungsgrad p von 1,1 bis 3,0 eingesetzt. Aus anwendungstechnischer Sicht sind solche Alkyl- und/oder Alkenyloligoglykoside bevorzugt, deren Oligomerisierungsgrad kleiner als 1,7 ist und insbesondere zwischen 1,2 und 1,4 liegt. Der Alkyl- bzw. Alkenylrest R1 kann sich von primären Alkoholen mit 4 bis 11, vorzugsweise 8 bis 10 Kohlenstoffatomen ableiten. Typische Beispiele sind Butanol, Capronalkohol, Caprylalkohol, Caprinalkohol und Undecylalkohol sowie deren technische Mischungen, wie sie beispielsweise bei der Hydrierung von technischen Fettsäuremethylestern oder im Verlauf der Hydrierung von Aldehyden aus der Roelen'schen Oxosynthese erhalten werden. Bevorzugt sind Alkyloligo-glucoside der Kettenlänge C8-Cι0 (DP = 1 bis 3), die als Vorlauf bei der destillativen Auftrennung von technischem C8-Cι8-Kokosfettalkohol anfallen und mit einem Anteil von weniger als 6 Gew.-% Cι2-Alkohol verunreinigt sein können sowie Alkyl- oligoglucoside auf Basis technischer Cg/u-Oxoalkohole (DP = 1 bis 3). Der Alkyl- bzw. Alkenylrest R1 kann sich ferner auch von primären Alkoholen mit 12 bis 22, vorzugsweise 12 bis 14 Kohlenstoffatomen ableiten. Typische Beispiele sind Laurylalkohol, My- ristylalkohol, Cetylalkohol, Palmoleylalkohol, Stearylalkohol, Isostearylalkohol, Oleylalkohol, Elaidyl-alkohol, Petroselinylalkohol, Arachylalkohol, Gadoleylalkohol, Behenylalkohol, Erucylalkohol, Brassidylalkohol sowie deren technische Gemische, die wie oben beschrieben erhalten werden kön-nen. Bevorzugt sind Alkyloligoglucoside auf Basis von gehärtetem Cι2 ι4-Kokosalkohol mit einem DP von 1 bis 3.The alkyl and / or alkenyl oligoglycosides can be derived from aldoses or ketoses with 5 or 6 carbon atoms, preferably glucose. The preferred alkyl and / or alkenyl oligoglycosides are thus alkyl and / or alkenyl oligoglucosides. The index number p in the general formula (I) indicates the degree of oligomerization (DP), ie the distribution of mono- and oligoglycosides, and stands for a number between 1 and 10. While p must always be an integer in a given compound and especially here can assume the values p = 1 to 6, the value p for a certain alkyl oligoglycoside is an analytically determined arithmetic parameter, which usually represents a fractional number. Alkyl and / or alkenyl oligoglycosides with an average degree of oligomerization p of 1.1 to 3.0 are preferably used. From an application point of view, preference is given to those alkyl and / or alkenyl oligoglycosides whose degree of oligomerization is less than 1.7 and in particular between 1.2 and 1.4. The alkyl or alkenyl radical R 1 can be derived from primary alcohols having 4 to 11, preferably 8 to 10, carbon atoms. Typical examples are butanol, capronic alcohol, caprylic alcohol, capric alcohol and undecyl alcohol and their technical mixtures, such as are obtained, for example, in the hydrogenation of technical fatty acid methyl esters or in the course of the hydrogenation of aldehydes from Roelen's oxosynthesis. Preferred are alkyl oligo-glucosides of chain length C 8 -Cι 0 (DP = 1 to 3), which are obtained as a preliminary step in the separation of technical C 8 -C 8 coconut fatty alcohol by distillation and with a proportion of less than 6% by weight Cι 2 alcohol may be contaminated and alkyl oligoglucoside based on technical Cg / u-oxo alcohols (DP = 1 to 3). The alkyl or alkenyl radical R 1 can also be derived from primary alcohols having 12 to 22, preferably 12 to 14, carbon atoms. Typical examples are lauryl alcohol, myristyl alcohol, cetyl alcohol, palmoleyl alcohol, stearyl alcohol, isostearyl alcohol, oleyl alcohol, elaidyl alcohol, petroselinyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol, brassidyl alcohol and the technical mixtures described above, which can be obtained as well as their technical mixtures. Alkyl oligoglucosides based on hardened C 2 -C 4 coco alcohol with a DP of 1 to 3 are preferred.
Die Alkyloligoglucoside werden in Mengen von 0,5 bis 20 Gew. %, vorzugsweise 2,5 bis 15 und besonders bevorzugt 5 bis 10 Gew.% - bezogen auf die Waschzubereitung - eingesetzt.The alkyl oligoglucosides are used in amounts of 0.5 to 20% by weight, preferably 2.5 to 15 and particularly preferably 5 to 10% by weight, based on the washing preparation.
Amphotere TensideAmphoteric surfactants
Typische Beispiele für amphotere - auch unter „zwitterionische Tenside" geführt - sind Alkylbetaine, Alkylamidobetaine, Aminopropionate, Aminoglycinate, Imidazoliniumbetaine und Sulfobetaine. Bei den genannten Tensiden handelt es sich ausschließlich um bekannte Verbindungen. Hinsichtlich Struktur und Herstellung dieser Stoffe sei auf einschlägige Übersichtsarbeiten beispielsweise J.Falbe (ed.), "Surfactants in Consumer Products", Springer Verlag, Berlin, 1987, S. 54-124 oder J.Falbe (ed.), "Katalysatoren, Tenside und Mineralöladditive", Thieme Verlag, Stuttgart, 1978, S. 123-217 verwiesen.Typical examples of amphoteric - also listed under "zwitterionic surfactants" - are alkyl betaines, alkyl amido betaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines. The surfactants mentioned are exclusively known compounds .Falbe (ed.), "Surfactants in Consumer Products", Springer Verlag, Berlin, 1987, pp. 54-124 or J.Falbe (ed.), "Catalysts, surfactants and mineral oil additives", Thieme Verlag, Stuttgart, 1978, Pp. 123-217.
BetaineBetaine
Betaine stellen bekannte Tenside dar, die überwiegend durch Carboxyalkylierung, vorzugsweise Carb-oxymethylierung von aminischen Verbindungen hergestellt werden. Vorzugsweise werden die Ausgangsstoffe mit Halogencarbonsäuren oder deren Salzen, insbesondere mit Natriumchloracetat kondensiert, wobei pro Mol Betain ein Mol Salz gebildet wird. Ferner ist auch die Anlagerung von ungesättigten Carbonsäuren, wie beispielsweise Acrylsäure möglich. Zur Nomenklatur und insbesondere zur Unterscheidung zwischen Betainen und "echten" Amphotensiden sei auf den Beitrag von U.PIoog in Seifen-Öle-Fette-Wachse, 108. 373 (1982) verwiesen. Weitere Übersichten zu diesem Thema finden sich beispielsweise von A.O'Lennick et al. in HAPPI, Nov. 70 (1986), S.Holzman et al. in Tens. Surf.Det. 23, 309 (1986), R.Bibo et al. in Soap Cosm.Chem.Spec, Apr. 46 (1990) und P.EIIis et al. in Euro Cosm. 1, 14 (1994). Beispiele für geeignete Betaine stellen die Carboxyalkylierungsprodukte von sekundären und insbesondere tertiären Aminen dar, die der Formel (II) folgen, R3 Betaines are known surfactants which are predominantly produced by carboxyalkylation, preferably carboxymethylation, of aminic compounds. The starting materials are preferably condensed with halocarboxylic acids or their salts, in particular with sodium chloroacetate, one mol of salt being formed per mole of betaine. The addition of unsaturated carboxylic acids, such as acrylic acid, is also possible. Regarding the nomenclature and in particular the distinction between betaines and "real" amphoteric surfactants, reference is made to U.PIoog's contribution in Seifen-Öle-Fette-Wwachs, 108, 373 (1982). Further overviews on this topic can be found for example by A. O'Lennick et al. in HAPPI, Nov. 70 (1986), S. Holzman et al. in tens. Surf.Det. 1986, 23: 309, R.Bibo et al. in Soap Cosm. Chem. Spec, Apr. 46 (1990) and P.EIIis et al. in Euro Cosm. 1, 14 (1994). Examples of suitable betaines are the carboxyalkylation products of secondary and in particular tertiary amines which follow the formula (II) R 3
II
R2-N-(CH2)nCOOX (II)R 2 -N- (CH 2 ) n COOX (II)
II
R4 R 4
in der R2 für Alkyl- und/oder Alkenylreste mit 6 bis 22 Kohlenstoffatomen, R3 für Wasserstoff oder Alkylreste mit 1 bis 4 Kohlenstoffatomen, R4 für Alkylreste mit 1 bis 4 Kohlenstoffatomen, n für Zahlen von 1 bis 6 und X für ein Alkali- und/oder Erdalkalimetall oder Ammonium steht. Typische Beispiele sind die Carboxymethylierungsprodukte von Hexylmethylamin, Hexyldimethylamin, Octyldimethylamin, De-cyldimethylamin, Dodecylmethylamin, Dodecyldimethylamin, Dodecylethylmethylamin, Ci2/ι4-Kokosal- kyldimethylamin, Myristyldimethylamin, Cetyldimethylamin, Stearyldimethylamin, Stearylethylmethyl-amin, Oleyldimethylamin, Cι6/i8-Talgalkyldimethylamin sowie deren technische Gemische.in which R 2 for alkyl and / or alkenyl radicals with 6 to 22 carbon atoms, R 3 for hydrogen or alkyl radicals with 1 to 4 carbon atoms, R 4 for alkyl radicals with 1 to 4 carbon atoms, n for numbers from 1 to 6 and X for a Alkali and / or alkaline earth metal or ammonium. Typical examples are the carboxymethylation products of hexylmethylamine, hexyldimethylamine, octyldimethylamine, De-cyldimethylamin, dodecylmethylamine, dodecyldimethylamine, Dodecylethylmethylamin, C i2 / ι kyldimethylamin 4 -Kokosal-, myristyldimethylamine, cetyldimethylamine, stearyldimethylamine, Stearylethylmethyl-amine, oleyl dimethyl amine, Cι 6 / i 8 - Tallow alkyl dimethylamine and their technical mixtures.
Weiterhin kommen auch Carboxyalkylierungsprodukte von Amidoaminen in Betracht, die der Formel (III) folgen,Also suitable are carboxyalkylation products of amidoamines which follow the formula (III)
R5CO-NH-(CH2)rn-N-(CH2)nCOOX (III)R 5 CO-NH- (CH 2 ) rn -N- (CH 2 ) n COOX (III)
II
in der R5CO für einen aliphatischen Acylrest mit 6 bis 22 Kohlenstoffatomen und 0 oder 1 bis 3 Doppelbindungen, m für Zahlen von 1 bis 3 steht und R3, R4, n und X die oben angegebenen Bedeutungen haben. Typische Beispiele sind Umsetzungsprodukte von Fettsäuren mit 6 bis 22 Kohlen-stoffatomen, namentlich Capronsäure, Caprylsäure, Ca- prinsäure, Laurinsäure, Myristinsäure, Palmitinsäure, Palmoleinsäure, Stearinsäure, Isostearinsäure, Ölsäure, Elaidinsäure, Petroselinsäure, Linol-säure, Linolensäure, Elaeostearinsäure, Arachinsäure, Gadoleinsäure, Behensäure und Erucasäure so-wie deren technische Gemische, mit N,N-Dimethylaminoethylamin, N,N-Dimethylaminopropylamin, N,N-Diethylaminoethylamin und N,N-Diethylaminopropylamin, die mit Natriumchloracetat kondensiert werden. Bevorzugt ist der Einsatz eines Kondensationsproduktes von C8/i8- Kokosfettsäure-N,N-dime-thylaminopropylamid mit Natriumchloracetat.in which R 5 CO represents an aliphatic acyl radical having 6 to 22 carbon atoms and 0 or 1 to 3 double bonds, m represents numbers from 1 to 3 and R 3 , R 4 , n and X have the meanings given above. Typical examples are reaction products of fatty acids with 6 to 22 carbon atoms, namely caproic acid, caprylic acid, capric acid, lauric acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, araachearic acid , Gadoleic acid, behenic acid and erucic acid as well as their technical mixtures with N, N-dimethylaminoethylamine, N, N-dimethylaminopropylamine, N, N-diethylaminoethylamine and N, N-diethylaminopropylamine, which are condensed with sodium chloroacetate. Preferred is the use of a condensation product of C 8 / i 8 - Coconut fatty acid N, N-dime-thylaminopropylamid with sodium chloroacetate.
Weiterhin kommen als geeignete Ausgangsstoffe für die im Sinne der Erfindung einzusetzenden Betaine auch Imidazoline in Betracht, die der Formel (IV) folgen,
Figure imgf000008_0001
(IV)
Furthermore, suitable starting materials for the betaines to be used in accordance with the invention are also imidazolines which follow the formula (IV)
Figure imgf000008_0001
(IV)
in der R6 für einen Alkylrest mit 5 bis 21 Kohlenstoffatomen, R7 für eine Hydroxylgruppe, einen OCOR6- oder NHCOR7-Rest und m für 2 oder 3 steht. Auch bei diesen Substanzen handelt es sich um bekannte Stoffe, die beispielsweise durch cydisierende Kondensation von 1 oder 2 Mol Fettsäure mit mehrwertigen Aminen, wie beispielsweise Aminoethylethanolamin (AEEA) oder Diethylentriamin erhalten werden können. Die entsprechenden Carboxyalkylierungsprodukte stellen Gemische unterschiedlicher offen- kettiger Betaine dar. Typische Beispiele sind Kondensationsprodukte der oben genannten Fettsäuren mit AEEA, vorzugsweise Imidazoline auf Basis von Laurinsäure oder wiederum Cι2 ι4-Kokosfettsäure, die anschließend mit Natriumchloracetat betainisiert werden. Die im Sinne der vorliegenden Erfindung bevorzugt eingesetzten amphoteren Tenside sind Betaine vom Typ des Cocamidopropylbetains und Sodium Cocoamphoacetate. Die amphoteren Tenside werden in Mengen von 0,5 bis 30 Gew. %, vorzugsweise 2,5 bis 20 Gew. % und besonders bevorzugt 9 bis 19 Gew. % - bezogen auf die Waschzubereitungen, eingesetzt.in which R 6 is an alkyl radical having 5 to 21 carbon atoms, R 7 is a hydroxyl group, an OCOR 6 or NHCOR 7 radical and m is 2 or 3. These substances are also known substances which can be obtained, for example, by the condensing condensation of 1 or 2 moles of fatty acid with polyhydric amines, such as, for example, aminoethylethanolamine (AEEA) or diethylenetriamine. The corresponding carboxyalkylation products are mixtures of different open-chain betaines. Typical examples are condensation products of the above-mentioned fatty acids with AEEA, preferably imidazolines based on lauric acid or again C 2 -C 4 coconut fatty acid, which are subsequently betainized with sodium chloroacetate. The preferred amphoteric surfactants for the purposes of the present invention are betaines of the cocamidopropyl betaine type and sodium cocoamphoacetate. The amphoteric surfactants are used in amounts of 0.5 to 30% by weight, preferably 2.5 to 20% by weight and particularly preferably 9 to 19% by weight, based on the washing preparations.
Kationpolymerecationic polymers
Geeignete kationische Polymere sind beispielsweise kationische Cellulosederivate, wie z.B. eine quaternierte Hydroxyethylcellulose, die unter der Bezeichnung Polymer JR 400® von Amerchol erhältlich ist, kationische Stärke, Copolymere von Diallylammoniumsalzen und Acrylamiden, quaternierte Vinyl-pyrrolidon/Vinyl-imidazol-Polymere, wie z.B. Luviquat® (BASF), Kondensationsprodukte von Polygly-colen und Aminen, quaternierte Kollagenpolypeptide, wie beispielsweise Lauryldimonium hydroxypropyl hydrolyzed collagen (Lamequat®L/Grünau), quaternierte Weizenpolypeptide, Polyethylenimin, kationische Siliconpolymere, wie z.B. Amidomethicone, Copolymere der Adipinsäure und Dimethylaminohydroxypropyldiethylentriamin (Cartaretine®/Sandoz), Copolymere der Acrylsäure mit Dimethyldiallyl-ammoniumchlorid (Merquat® 550/Chemviron), Polyaminopolyamide, wie z.B. beschrieben in der FR-A 2252840 sowie deren vernetzte wasserlöslichen Polymere, kationische Chitinderivate, wie beispiels-weise quaterniertes Chitosan, gegebenenfalls mikrokristallin verteilt, Kondensationsprodukte aus Diha- logenalkylen, wie z.B. Dibrombutan mit Bisdialkylaminen, wie z.B. Bis-Dimethylamino-1,3- propan, kationischer Guar-Gum, wie z.B. Jaguar® CBS, Jaguar® C-17, Jaguar® C-16 der Firma Celanese, quaternierte Ammoniumsalz-Polymere, wie z.B. Mirapol® A-15, Mirapol® AD-1, Mirapol® AZ-1 der Firma Miranol.Suitable cationic polymers are, for example, cationic cellulose derivatives, such as, for example, a quaternized hydroxyethyl cellulose, which is available under the name Polymer JR 400® from Amerchol, cationic starch, copolymers of diallylammonium salts and acrylamides, quaternized vinyl-pyrrolidone / vinyl-imidazole polymers, such as, for example, luviquat ® (BASF), condensation products of polyglycols and amines, quaternized collagen polypeptides, such as, for example, lauryldimonium hydroxypropyl hydrolyzed collagen (Lamequat®L / Grünau), quaternized wheat polypeptides, polyethyleneimine, cationic silicone polymers, such as, for example, amidomethicones, copolymers of adipodinoxypropylene acid and dimethylaminohydroxyethylenediaminetroxyne diaminohydroxyethylenediaminetroxyne diaminohydroxylacetaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodiaminodi ... / Sandoz), copolymers of acrylic acid with dimethyldiallyl ammonium chloride (Merquat® 550 / Chemviron), polyaminopolyamides, as described for example in FR-A 2252840, and their crosslinked water-soluble polymers, cationic chitin derivatives, such as quaternized chit osan, optionally microcrystalline, condensation products from dihaloalkylene, such as dibromobutane with bisdialkylamines, such as bis-dimethylamino-1,3- propane, cationic guar gum, such as Jaguar® CBS, Jaguar® C-17, Jaguar® C-16 from Celanese, quaternized ammonium salt polymers, such as Mirapol® A-15, Mirapol® AD-1, Mirapol® AZ -1 from Miranol.
Kationpolymere werden in den erfindungsgemäßen Mitteln in Mengen von 0,02 bis 5 Gew.%, vorzugsweise 0,05 bis 3 Gew.% und besonders bevorzugt in Mengen von 0,1 bis 2 Gew.% eingesetzt. Zur optimalen Umsetzung des positiven synergistischen Konditionierungseffektes der Kombination von Kation polymeren und vordispergierten Wachsdispersionen sollten die mittleren Molekulargewichte der Kationpolymere zwischen 5000 und 1000000, vorzugsweise zwischen 8000 und 500000 liegen und besonders bevorzugt zwischen 10000 und 400000.Cation polymers are used in the agents according to the invention in amounts of 0.02 to 5% by weight, preferably 0.05 to 3% by weight and particularly preferably in amounts of 0.1 to 2% by weight. For optimal implementation of the positive synergistic conditioning effect of the combination of cationic polymers and predispersed wax dispersions, the average molecular weights of the cationic polymers should be between 5,000 and 1,000,000, preferably between 8,000 and 500,000 and particularly preferably between 10,000 and 400,000.
Besonders bevorzugt sind als Kationpolymere kationisches Guar-Gum und/oder quaternierte Ammoniumsalz-Polymere.Cationic guar gum and / or quaternized ammonium salt polymers are particularly preferred as cation polymers.
Kationpolymere werden in den erfindungsgemäßen Waschzubereitungen in Mengen von 0,1 bis 5 Gew.%, vorzugsweise 0,5 bis 4 Gew.% und besonders bevorzugt 1 bis 3 Gew. % - bezogen auf die Waschzubereitungen eingesetzt.Cation polymers are used in the washing preparations according to the invention in amounts of 0.1 to 5% by weight, preferably 0.5 to 4% by weight and particularly preferably 1 to 3% by weight, based on the washing preparations.
Wachsdispersionenwax dispersions
In den Waschzubereitungen können vordispergierte Wachsdispersionen in Mengen von 0 bis 5 Gew. %, vorzugsweise 0,005 bis 3,5 Gew.% und besonders bevorzugt in Mengen von 0,01 bis 3,1 Gew. % eingesetzt werden.Predispersed wax dispersions can be used in the washing preparations in amounts of 0 to 5% by weight, preferably 0.005 to 3.5% by weight and particularly preferably in amounts of 0.01 to 3.1% by weight.
Der Anteil der in den Wachsdispersionen enthaltenen Wachskörper beträgt 10 bis 40 Gew.%, vorzugsweise 15 bis 35 Gew.% und besonders bevorzugt 20 bis 30 Gew. % - bezogen auf die vordispergierte Wachsdispersion. Als Wachskörper kommen in den Wachsdispersionen in Frage: Alkylenglycolester, Fettsäurealkanolamide, Partialglyceride, Ester von mehrwertigen, gegebenenfalls hydroxysubstituierten Carbonsäuren, Fettalkohole, Fettketone, Fettaldehyde, Fettether, Fettcarbonate, Ringöffnungsprodukte von Olefinepoxiden sowie deren Mischungen.The proportion of the wax bodies contained in the wax dispersions is 10 to 40% by weight, preferably 15 to 35% by weight and particularly preferably 20 to 30% by weight, based on the predispersed wax dispersion. Possible wax bodies in the wax dispersions are: alkylene glycol esters, fatty acid alkanolamides, partial glycerides, esters of polyvalent, optionally hydroxy-substituted carboxylic acids, fatty alcohols, fatty ketones, fatty aldehydes, fatty ethers, fatty carbonates, ring-opening products of olefin epoxides and mixtures thereof.
Bei den Alkylenglycolestern, die die bevorzugten Wachskörper bilden, handelt es sich üblicherweise um Mono- und/oder Diester von Alkylenglycolen, die der Formel (V) folgen,The alkylene glycol esters which form the preferred wax bodies are usually mono- and / or diesters of alkylene glycols which follow the formula (V)
R8CO(OA)nOR9 (V)R 8 CO (OA) n OR 9 (V)
in der R8CO für einen linearen oder verzweigten, gesättigten oder ungesättigten Acylrest mit 6 bis 22 Kohlenstoffatomen, R9 für Wasserstoff oder R8CO und A für einen linearen oder verzweigten Alkylenrest mit 2 bis 4 Kohlenstoffatomen und n für Zahlen von 1 bis 5 steht. Typische Beispiele sind Mono- und/oder Diester von Ethylenglycol, Propylenglycol, Diethylenglycol, Dipropylenglycol, Triethylenglycol oder Tetraethylenglycol mit Fettsäuren mit 6 bis 22, vorzugsweise 12 bis 18 Kohlenstoffatomen als da sind: Capronsäure, Caprylsäure, 2-Ethylhexansäure, Caprinsäure, Laurinsäure, Isotridecansäure, My- ristinsäure, Palmitinsäure, Palmoleinsäure, Stearinsäure, Isostearinsäure, Ölsäure, Elaidinsäure, Petroselinsäure, Linolsäure, Linolensäure, Elaeostearinsäure, Arachinsäure, Gadoleinsäure, Behensäure und Erucasäure sowie deren technische Mischungen. Besonders bevorzugt ist der Einsatz von Ethylenglycolmono- und/oder -distearat.in which R 8 CO is a linear or branched, saturated or unsaturated acyl radical having 6 to 22 carbon atoms, R 9 is hydrogen or R 8 CO and A is a linear or branched alkylene radical having 2 to 4 carbon atoms and n is a number from 1 to 5 stands. Typical examples are mono- and / or diesters of ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, triethylene glycol or tetraethylene glycol with fatty acids with 6 to 22, preferably 12 to 18 carbon atoms as there are: caproic acid, caprylic acid, 2-ethylhexanoic acid, capric acid, lauric acid, isotridecanoic acid, myristic acid, palmitic acid, palmoleic acid, stearic acid, isostearic acid, oleic acid, elaidic acid, petroselinic acid, linoleic acid, linolenic acid, linolenic acid Elaeostearic acid, arachic acid, gadoleic acid, behenic acid and erucic acid and their technical mixtures. The use of ethylene glycol mono- and / or distearate is particularly preferred.
Wassergehaltwater content
Aufgrund des hohen Öl- und Tensidanteils muß der Wasseranteil der Formulierungen relativ gering ausfallen. Eine gute physico-chemische Stabilität der Waschzubereitungen wurde erreicht, wenn der Gehalt an reinem Wasser maximal 55 Gew.%, vorzugsweise maximal 45 Gew.% und besonders bevorzugt maximal 35 Gew. % - bezogen auf die Waschzubereitung war.Due to the high oil and surfactant content, the water content of the formulations must be relatively low. Good physico-chemical stability of the washing preparations was achieved when the pure water content was at most 55% by weight, preferably at most 45% by weight and particularly preferably at most 35% by weight, based on the washing preparation.
Gewerbliche AnwendbarkeitIndustrial applicability
Die erfindungsgemäßen pflanzenölhaltigen Waschzubereitungen werden vorwiegend, jedoch nicht ausschließlich im Bereich der kosmetischen Produkte eingesetzt.The vegetable oil-containing washing preparations according to the invention are predominantly, but not exclusively, used in the field of cosmetic products.
Erfindungsgemäße Ausführungsformen der Waschzubereitungen enthalten:Embodiments of the washing preparations according to the invention contain:
(a) mindestens 25 Gew. % Pflanzenöle,(a) at least 25% by weight of vegetable oils,
(b) 0,5 bis 20 Gew.-% Alkylpolyglycoside,(b) 0.5 to 20% by weight of alkyl polyglycosides,
(c) 0,5 bis 20 Gew. % amphotere Tenside und(c) 0.5 to 20% by weight of amphoteric surfactants and
(d) maximal 55 Gew.-% Wasser,(d) a maximum of 55% by weight of water,
bevorzugt enthalten die erfindungsgemäßen Waschzubereitungenthe washing preparations according to the invention preferably contain
(a) mindestens 35 Gew. % Pflanzenöle,(a) at least 35% by weight of vegetable oils,
(b) 2,5 bis 15 Gew.-% Alkylpolyglycoside,(b) 2.5 to 15% by weight of alkyl polyglycosides,
(c) 2,5 bis 20 Gew. % amphotere Tenside und(c) 2.5 to 20% by weight of amphoteric surfactants and
(d) maximal 45 Gew.-% Wasser(d) a maximum of 45% by weight water
besonders bevorzugt enthalten siethey particularly preferably contain
(a) mindestens 45 Gew. % Pflanzenöle,(a) at least 45% by weight of vegetable oils,
(b) 5 bis 10 Gew.-% Alkylpolyglycoside,(b) 5 to 10% by weight of alkyl polyglycosides,
(c) 9 bis 19 Gew. % amphotere Tenside und(c) 9 to 19% by weight of amphoteric surfactants and
(d) maximal 35 Gew.-% Wasser, bevorzugter(d) a maximum of 35% by weight of water, preferred
(a) mindestens 45 Gew. % Pflanzenöle,(a) at least 45% by weight of vegetable oils,
(b) 5 bis 10 Gew.-% Alkylpolyglycoside,(b) 5 to 10% by weight of alkyl polyglycosides,
(c) 9 bis 19 Gew. % amphotere Tenside,(c) 9 to 19% by weight of amphoteric surfactants,
(d) maximal 35 Gew.-% Wasser,(d) a maximum of 35% by weight of water,
(e) 0,1 bis 5 Gew. % Kationpolymere,(e) 0.1 to 5% by weight of cation polymers,
speziell bevorzugtespecially preferred
(a) mindestens 45 Gew. % Pflanzenöle,(a) at least 45% by weight of vegetable oils,
(b) 5 bis 10 Gew.-% Alkylpolyglycoside,(b) 5 to 10% by weight of alkyl polyglycosides,
(c) 9 bis 16 Gew. % Betaine,(c) 9 to 16% by weight betaines,
(d) maximal 35 Gew.-% Wasser,(d) a maximum of 35% by weight of water,
(e) 1 bis 3 Gew. Kationpolymere und(e) 1 to 3% by weight of cation polymers and
(f) 0,005 bis 3,5 Gew. % Wachsdispersionen(f) 0.005 to 3.5% by weight wax dispersions
mit der Maßgabe, dass sich die Angaben mit Wasser und gegebenenfalls weiteren üblichen Hilfs- und Zusatzstoffen zu 100 Gew.-% addieren.with the proviso that the information with water and possibly other customary auxiliaries and additives add up to 100% by weight.
Die erfindungsgemäßen Zubereitungen können als kosmetische und/oder pharmazeutische Zubereitungen, wie beispielsweise Haarshampoos, feste Seifenstücke, Waschlotionen, Schaumbäder, Duschbädern und vorzugsweise Ölbädern dienen.The preparations according to the invention can serve as cosmetic and / or pharmaceutical preparations, such as, for example, hair shampoos, solid bars of soap, washing lotions, bubble baths, shower baths and preferably oil baths.
Als weitere Hilfs- und Zusatzstoffe können sie ferner Emulgatoren, weitere Olkörper, Perlglanzwachse, Konsistenzgeber, Überfettungsmittel, Stabilisatoren, weitere Polymere, Siliconverbindungen, Lecithine, Phospholipide, biogene Wirkstoffe, Antioxidantien, Antischuppenmittel, Filmbildner, Hydrotrope, Solubilisatoren, Konservierungsmittel, Parfümöle, Farbstoffe und dergleichen enthalten. As further auxiliaries and additives, they can also contain emulsifiers, further oil bodies, pearlescent waxes, consistency agents, superfatting agents, stabilizers, further polymers, silicone compounds, lecithins, phospholipids, biogenic active substances, antioxidants, antidandruff agents, film formers, hydrotropes, solubilizers, preservatives, perfume oils, dyes and dyes the like included.
Emulgatorenemulsifiers
Neben den bereits erwähnten bevorzugten Tensiden kommen als Emulgatoren beispielsweise nichtionogene Stoffe aus mindestens einer der folgenden Gruppen in Frage:In addition to the preferred surfactants mentioned above, suitable emulsifiers are, for example, nonionic substances from at least one of the following groups:
> 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, an Alkylphenole mit 8 bis 15 C-Atomen in der Alkylgruppe sowie Alkylamine mit 8 bis 22 Kohlenstoffatomen im Alkylrest;> Adducts 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, with alkylphenols with 8 to 15 carbon atoms in the alkyl group and Alkylamines with 8 to 22 carbon atoms in the alkyl radical;
> Anlagerungsprodukte von 1 bis 15 Mol Ethylenoxid an Ricinusöl und/oder gehärtetes Ridnusöl;> Addition products of 1 to 15 moles of ethylene oxide with castor oil and / or hardened Ridnusöl;
> Anlagerungsprodukte von 15 bis 60 Mol Ethylenoxid an Ricinusöl und/oder gehärtetes Ricinusöl;> Adducts of 15 to 60 moles of ethylene oxide with castor oil and / or hardened castor oil;
> Partialester von Glycerin und/oder Sorbitan mit ungesättigten, linearen oder gesättigten, verzweigten Fettsäuren mit 12 bis 22 Kohlenstoffatomen und/oder Hydroxycarbonsäuren mit 3 bis 18 Kohlenstoffatomen sowie deren Addukte mit 1 bis 30 Mol Ethylenoxid;> Partial esters of glycerol and / or sorbitan with unsaturated, linear or saturated, branched fatty acids with 12 to 22 carbon atoms and / or hydroxycarboxylic acids with 3 to 18 carbon atoms and their adducts with 1 to 30 moles of ethylene oxide;
> Partialester von Polyglycerin (durchschnittlicher Eigenkondensationsgrad 2 bis 8), Polyethylenglycol (Molekulargewicht 400 bis 5000), Trimethylolpropan, Pentaerythrit, Zuckeralkoholen (z.B. Sorbit), Alkylglucosiden (z.B. Methylglucosid, Butylglucosid, Laurylglucosid) sowie Polyglucosiden (z.B. Cellulose) mit gesättigten und/oder ungesättigten, linearen oder verzweigten Fettsäuren mit 12 bis 22 Kohlenstoffatomen und/oder Hydroxycarbonsäuren mit 3 bis 18 Kohlenstoffatomen sowie deren Addukte mit 1 bis 30 Mol Ethylenoxid;> Partial esters of polyglycerin (average degree of self-condensation 2 to 8), polyethylene glycol (molecular weight 400 to 5000), trimethylolpropane, pentaerythritol, sugar alcohols (e.g. sorbitol), alkyl glucosides (e.g. methyl glucoside, butyl glucoside, lauryl glucoside) and polyglucosides saturated (e.g. cellulose) unsaturated, linear or branched fatty acids with 12 to 22 carbon atoms and / or hydroxycarboxylic acids with 3 to 18 carbon atoms and their adducts with 1 to 30 moles of ethylene oxide;
> Mischester aus Pentaerythrit, Fettsäuren, Citronensäure und Fettalkohol gemäß DE 1165574 PS und/oder Mischester von Fettsäuren mit 6 bis 22 Kohlenstoffatomen, Methylglucose und Polyolen, vorzugsweise Glycerin oder Polyglycerin.> Mixed esters of pentaerythritol, fatty acids, citric acid and fatty alcohol according to DE 1165574 PS and / or mixed esters of fatty acids with 6 to 22 carbon atoms, methyl glucose and polyols, preferably glycerol or polyglycerol.
> Mono-, Di- und Trialkylphosphate sowie Mono-, Di- und/oder Tri-PEG-alkylphosphate und deren Salze;> Mono-, di- and trialkyl phosphates and mono-, di- and / or tri-PEG-alkyl phosphates and their salts;
> Wollwachsalkohole;> Wool wax alcohols;
> Polysiloxan-Polyalkyl-Polyether-Copolymere bzw. entsprechende Derivate;> Polysiloxane-polyalkyl-polyether copolymers or corresponding derivatives;
> Block-Copolymere z.B. Polyethylenglycol-30 Dipolyhydroxystearate;> Block copolymers e.g. Polyethylene glycol 30 dipolyhydroxystearate;
> Polymeremulgatoren, z.B. Pemulen-Typen (TR-l/TR-2) von Goodrich;> Polymer emulsifiers, e.g. Pemulen types (TR-1 / TR-2) from Goodrich;
> Polyalkylenglycole sowie> Polyalkylene glycols as well
> Glycerincarbonat.> Glycerine carbonate.
n Ethylenoxidanlagerungsprodukten Ethylene Oxide
Die Anlagerungsprodukte von Ethylenoxid und/oder von Propylenoxid an Fettalkohole, Fettsäuren, Alkylphenole oder an Ricinusöl stellen bekannte, im Handel erhältliche Produkte dar. Es handelt sich dabei um Homologengemische, deren mittlerer Alkoxy- lierungsgrad dem Verhältnis der Stoffmengen von Ethylenoxid und/ oder Propylenoxid und Substrat, mit denen die Anlagerungsreaktion durchgeführt wird, entspricht. C12 ι8- Fettsäuremono- und -diester von Anlagerungsprodukten von Ethylenoxid an Glycerin sind aus DE 2024051 PS als Rückfettungsmittel für kosmetische Zubereitungen bekannt.The adducts of ethylene oxide and / or of propylene oxide with fatty alcohols, fatty acids, alkylphenols or with castor oil are known, commercially available products. These are mixtures of homologs whose average degree of alkoxylation is the ratio of the amounts of ethylene oxide and / or propylene oxide and Substrate with which the addition reaction is carried out corresponds. C 12 ι 8 - fatty acid monoesters and diesters of adducts of ethylene oxide with glycerol are known from DE 2024051 PS as refatting agents for cosmetic preparations.
> Partialglyceride> Partial glycerides
Typische Beispiele für geeignete Partialglyceride sind Hydroxystearinsäure- monoglycerid, Hydroxystearinsäurediglycerid, Isostearinsäuremonoglycerid,Typical examples of suitable partial glycerides are hydroxystearic acid monoglyceride, hydroxystearic acid diglyceride, isostearic acid monoglyceride,
Isostearinsäurediglycerid, Ölsäuremonoglycerid, Ölsäurediglycerid, Ricinolsäure- moglycerid, Ricinolsäurediglycerid, Linolsäuremonoglycerid, Linolsäurediglycerid, Linolensäuremonoglycerid, Linolensäurediglycerid, Erucasäuremonoglycerid,Isostearic acid diglyceride, oleic acid monoglyceride, oleic acid diglyceride, ricinoleic acid moglyceride, ricinoleic acid diglyceride, linoleic acid monoglyceride, linoleic acid diglyceride, linolenic acid monoglyceride, linolenic acid diglyceride, erucic acid monoglyceride
Erucasäurediglycerid, Weinsäuremonoglycerid, Weinsäurediglycerid, Citronensäure- monoglycerid, Citronendiglycerid, Apfelsäuremonoglycerid, Apfelsäurediglycerid sowie deren technische Gemische, die untergeordnet aus dem Herstellungsprozeß noch geringe Mengen an Triglycerid enthalten können. Ebenfalls geeignet sind Anlagerungsprodukte von 1 bis 30, vorzugsweise 5 bis 10 Mol Ethylenoxid an die genannten Partialglyceride.Erucic acid diglyceride, tartaric acid monoglyceride, tartaric acid diglyceride, citric acid monoglyceride, citric diglyceride, malic acid monoglyceride, malic acid diglyceride and their technical mixtures, which may still contain small amounts of triglyceride from the manufacturing process. Addition products of 1 to 30, preferably 5 to 10, mol of ethylene oxide onto the partial glycerides mentioned are also suitable.
> Sorbitanester> Sorbitan esters
Als Sorbitanester kommen Sorbitanmonoisostearat, Sorbitansesquiisostearat, Sorbitan-diisostearat, Sorbitantriisostearat, Sorbitanmonooleat, Sorbitansesquioleat, Sorbitan-dioleat, Sorbitantrioleat, Sorbitanmonoerucat, Sorbitansesquierucat, Sorbitandierucat, Sorbitantrierucat, Sorbitanmonoricinoleat, Sorbitansesquiricinoleat, Sorbitandiricinoleat, Sorbitantriricinoleat, Sorbitanmonohydroxystearat, Sorbitan- sesquihydroxystearat, Sorbitandihydroxystearat, Sorbitantrihydroxystearat,As sorbitan sorbitan, sorbitan sesquiisostearate, sorbitan diisostearate, sorbitan triisostearate, sorbitan monooleate, sorbitan dioleate, trioleate, Sorbitanmonoerucat, Sorbitansesquierucat, Sorbitandierucat, Sorbitantrierucat, Sorbitanmonoricinoleat, Sorbitansesquiricinoleat, Sorbitandiricinoleat, Sorbitantriricinoleat, Sorbitanmonohydroxystearat, sorbitan come sesquihydroxystearat, Sorbitandihydroxystearat, Sorbitantrihydroxystearat,
Sorbitanmonotartrat, Sorbitansesqui-tartrat, Sorbitanditartrat, Sorbitantritartrat, Sorbitanmonocitrat, Sorbitansesquicitrat, Sorbitandicitrat, Sorbitantricitrat, Sorbitanmonomaleat, Sorbitansesquimaleat, Sorbitan-dimaleat, Sorbitantrimaleat sowie deren technische Gemische. Ebenfalls geeignet sind Anlagerungsprodukte von 1 bis 30, vorzugsweise 5 bis 10 Mol Ethylenoxid an die genannten Sorbitanester. > PolvglycerinesterSorbitan monotartrate, sorbitan sesqui-tartrate, sorbitan ditartrate, sorbitan tritartrate, sorbitan monocitrate, sorbitan sesquicitrate, sorbitan dicitrate, sorbitan tricitrate, sorbitan monomaleate, sorbitan sesquimaleate, sorbitan technical dimaleate and their sorbitan technical trimaleate. Addition products of 1 to 30, preferably 5 to 10, mol of ethylene oxide onto the sorbitan esters mentioned are also suitable. > Polyglycerol esters
Typische Beispiele für geeignete Polyglycerinester sind Polyglyceryl-2 Dipolyhydroxystearate (Dehymuls® PGPH), Polyglycerin-3-Diisostearate (Lameform® TGI), Polyglyceryl-4 Isostearate (Isolan® GI 34), Polyglyceryl-3 Oleate, Diisostearoyl Polyglyceryl-3 Diisostearate (Isolan® PDI), Polyglyceryl-3 Methylglucose Distearate (Tego Care® 450), Polyglyceryl-3 Beeswax (Cera Bellina®), Polyglyceryl-4 Caprate (Polyglycerol Caprate T2010/90), Polyglyceryl-3 Cetyl Ether (Chimexane® NL), Polyglyceryl-3 Distearate (Cremophor® GS 32) und Polyglyceryl Polyricinoleate (Admul® WOL 1403) Polyglyceryl Dimerate Isostearate sowie deren Gemische. Beispiele für weitere geeignete Polyolester sind die gegebenenfalls mit 1 bis 30 Mol Ethylenoxid umgesetzten Mono-, Di- und Triester von Trimethylolpropan oder Pentaerythrit mit Laurinsäure, Kokosfettsäure, Taigfettsäure, Palmitinsäure, Stearinsäure, Ölsäure, Behensäure und dergleichen.Typical examples of suitable polyglycerol esters are polyglyceryl-2 dipolyhydroxystearate (Dehymuls® PGPH), polyglycerol-3-diisostearate (Lameform® TGI), polyglyceryl-4 isostearate (Isolan® GI 34), polyglyceryl-3 oleate, diisostearoyl polyglyearyl-3 diisostearate ® PDI), Polyglyceryl-3 Methylglucose Distearate (Tego Care® 450), Polyglyceryl-3 Beeswax (Cera Bellina®), Polyglyceryl-4 Caprate (Polyglycerol Caprate T2010 / 90), Polyglyceryl-3 Cetyl Ether (Chimexane® NL), Polyglyceryl -3 Distearate (Cremophor® GS 32) and Polyglyceryl Polyricinoleate (Admul® WOL 1403) Polyglyceryl Dimerate Isostearate and their mixtures. Examples of other suitable polyol esters are the mono-, di- and triesters of trimethylolpropane or pentaerythritol with lauric acid, coconut fatty acid, taig fatty acid, palmitic acid, stearic acid, oleic acid, behenic acid and the like which are optionally reacted with 1 to 30 mol of ethylene oxide.
> Anionische Emulgatoren> Anionic emulsifiers
Typische anionische Emulgatoren sind aliphatische Fettsäuren mit 12 bis 22 Kohlenstoffatomen, wie beispielsweise Palmitinsäure, Stearinsäure oder Behensäure, sowie Dicarbonsäuren mit 12 bis 22 Kohlenstoffatomen, wie beispielsweise Azelainsäure oder Sebacinsäure.Typical anionic emulsifiers are aliphatic fatty acids with 12 to 22 carbon atoms, such as, for example, palmitic acid, stearic acid or behenic acid, and dicarboxylic acids with 12 to 22 carbon atoms, such as, for example, azelaic acid or sebacic acid.
OlkörperOlkörper
Neben den obligatorischen Ölen pflanzlichen Ursprungs können in den erfindungsgemäßenIn addition to the mandatory oils of vegetable origin, the invention can
Waschzubereitungen auch kleinere Mengen weiterer Olkörper eingesetzt werden, wie beispielsweise Guerbetalkohole auf Basis von Fettalkoholen mit 6 bis 18, vorzugsweise 8 bis 10 Kohlenstoffatomen, Ester von linearen C6-C22-Fettsäuren mit linearen oder verzweigten C6-C22-Fettalkoholen bzw. Ester von verzweigten C6-Cι3-Carbonsäuren mit linearen oder verzweigten C6-C22-Fettalkoholen, wie z.B. Myristylmyristat, Myristylpalmitat,Washing preparations also use smaller amounts of other oil bodies, such as Guerbet alcohols based on fatty alcohols having 6 to 18, preferably 8 to 10 carbon atoms, esters of linear C 6 -C 22 fatty acids with linear or branched C 6 -C 22 fatty alcohols or Esters of branched C 6 -C 3 carboxylic acids with linear or branched C 6 -C 22 fatty alcohols, such as myristyl myristate, myristyl palmitate,
Myristylstearat, Myristylisostearat, Myristyloleat, Myristylbehenat, Myristylerucat,Myristyl stearate, myristyl isostearate, myristyl oleate, myristyl behenate, myristyl erucate,
Cetyl myristat, Cetylpalmitat, Cetylstearat, Cetylisostearat, Cetyloleat, Cetylbehenat,Cetyl myristate, cetyl palmitate, cetyl stearate, cetyl isostearate, cetyl oleate, cetyl behenate,
Cetylerucat, Stearyl myristat, Stearylpa Imitat, Stearylstearat, Stearylisostearat, Stearyloleat,Cetylerucate, stearyl myristat, stearylpa imitation, stearyl stearate, stearyl isostearate, stearyl oleate,
Stearylbehenat, Stearylerucat, Isostearylmyristat, Isostearylpalmitat, Isostearylstearat,Stearyl behenate, stearyl erucate, isostearyl myristate, isostearyl palmitate, isostearyl stearate,
Isostearylisostearat, Isostearyloleat, Isostearylbehenat, Isostearyloleat, Oleylmyristat,Isostearyl isostearate, isostearyl oleate, isostearyl behenate, isostearyl oleate, oleyl myristate,
Oleylpalmitat, Oleylstearat, Oleylisostearat, Oleyloleat, Oleylbehenat, Oleylerucat, Behenylmyristat, Behenylpalmitat, Behenylstearat, Behenylisostearat, Behenyloleat, Behenylbehenat, Behenylerucat, Erucylmyristat, Erucylpalmitat, Erucylstearat, Erucylisostearat, Erucyloleat, Erucylbehenat und Erucylerucat. Daneben eignen sich Ester von linearen C6-C22-Fettsäuren mit verzweigten Alkoholen, insbesondere 2-Ethylhexanol, Ester von Cι8-C38-Alkylhydroxycarbonsäuren mit linearen oder verzweigten C6-C22- Fettalkoholen (vgl. DE 19756377 AI), insbesondere Dioctyl Malate, Ester von linearen und/oder verzweigten Fettsäuren mit mehrwertigen Alkoholen (wie z.B. Propylenglycol, Dimerdiol oder Trimertriol) und/oder Guerbetalkoholen, Triglyceride auf Basis C6-Cι0-Fett- säuren, flüssige Mono7Di-/Triglyceridmischungen auf Basis von C6-Cι8-Fettsäuren, Ester von C6-C22-Fettalkoholen und/oder Guerbetalkoholen mit aromatischen Carbonsäuren, insbesondere Benzoesäure, Ester von C2-Cι2-Dicarbonsäuren mit linearen oder verzweigten Alkoholen mit 1 bis 22 Kohlenstoffatomen oder Polyolen mit 2 bis 10 Kohlenstoffatomen und 2 bis 6 Hydroxylgruppen, verzweigte primäre Alkohole, substituierte Cyclohexane, lineare und verzweigte C6-C22-Fettalkoholcarbonate, wie z.B. Dicaprylyl Carbonate (Cetiol® CC), Guerbetcarbonate auf Basis von Fettalkoholen mit 6 bis 18, vorzugsweise 8 bis 10 C Atomen, Ester der Benzoesäure mit linearen und/oder verzweigten C6-C22-Alkoholen (z.B. Finsolv® TN), lineare oder verzweigte, symmetrische oder unsymmetrische Dialkylether mit 6 bis 22 Kohlenstoffatomen pro Alkylgruppe, wie z.B. Dicaprylyl Ether (Cetiol® OE), Ringöffnungsprodukte von epoxidierten Fettsäureestern mit Polyolen, Siliconöle (Cyclomethicone, Siliciummethicontypen u.a.) und/oder aliphatische bzw. naphthenische Kohlenwasserstoffe, wie z.B. wie Squalan, Squalen oder Dialkylcyclohexane.Oleyl palmitate, oleyl stearate, oleyl isostearate, oleyl oleate, oleyl behenate, olerlerucate, Behenyl myristate, behenyl palmitate, behenyl stearate, behenyl isostearate, behenyl oleate, behenyl behenate, behenylerucate, erucyl myristate, erucyl palmitate, erucyl stearate, erucyl isostearate, erucyl oleate, erucyl behenate and erucylerucate. In addition, esters of linear C 6 -C 22 fatty acids with branched alcohols, in particular 2-ethylhexanol, esters of C 8 -C 38 alkylhydroxycarboxylic acids with linear or branched C 6 -C 22 fatty alcohols (cf. DE 19756377 AI), in particular dioctyl malates, esters of linear and / or branched fatty acids with polyhydric alcohols (such as propylene glycol, dimer diol or trimer triol) and / or Guerbet alcohols, triglycerides based on C 6 -C0 0 fatty acids, liquid mono7 di / triglyceride mixtures based on C 6 -C 8 fatty acids, esters of C 6 -C 22 fatty alcohols and / or Guerbet alcohols with aromatic carboxylic acids, in particular benzoic acid, esters of C 2 -C 2 dicarboxylic acids with linear or branched alcohols having 1 to 22 carbon atoms or polyols 2 to 10 carbon atoms and 2 to 6 hydroxyl groups, branched primary alcohols, substituted cyclohexanes, linear and branched C 6 -C 22 fatty alcohol carbonates, such as, for example, dicaprylyl car bonate (Cetiol® CC), Guerbet carbonates based on fatty alcohols with 6 to 18, preferably 8 to 10 C atoms, esters of benzoic acid with linear and / or branched C 6 -C 22 alcohols (e.g. Finsolv® TN), linear or branched , symmetrical or asymmetrical dialkyl ethers with 6 to 22 carbon atoms per alkyl group, such as dicaprylyl ether (Cetiol® OE), ring opening products of epoxidized fatty acid esters with polyols, silicone oils (cyclomethicones, silicon methicone types etc.) and / or aliphatic or naphthenic hydrocarbons, such as squalane , Squalene or dialkylcyclohexanes.
Perlglanzwachsepearlescent
Als Perlglanzwachse kommen beispielsweise in Frage: Alkylenglycolester, speziell Ethylenglycoldistearat; Fettsäurealkanolamide, speziell Kokosfettsäurediethanolamid; Partialglyceride, speziell Stearinsäuremonoglycerid; Ester von mehrwertigen, gegebenenfalls hydroxy-substituierte Carbonsäuren mit Fettalkoholen mit 6 bis 22 Kohlenstoffatomen, speziell langkettige Ester der Weinsäure; Fettstoffe, wie beispielsweise Fettalkohole, Fettketone, Fettaldehyde, Fettether und Fettcarbonate, die in Summe mindestens 24 Kohlenstoffatome aufweisen, speziell Lauron und Distearylether; Fettsäuren wie Stearinsäure, Hydroxystearinsäure oder Behensäure, Ringöffnungsprodukte von Olefinepoxiden mit 12 bis 22 Kohlenstoffatomen mit Fettalkoholen. Konsistenzgeber und VerdickungsmittelPearlescent waxes that can be used are, for example: alkylene glycol esters, especially ethylene glycol distearate; Fatty acid alkanolamides, especially coconut fatty acid diethanolamide; Partial glycerides, especially stearic acid monoglyceride; Esters of polyvalent, optionally hydroxy-substituted carboxylic acids with fatty alcohols having 6 to 22 carbon atoms, especially long-chain esters of tartaric acid; Fatty substances, such as, for example, fatty alcohols, fatty ketones, fatty aldehydes, fatty ethers and fatty carbonates, which have a total of at least 24 carbon atoms, especially lauron and distearyl ether; Fatty acids such as stearic acid, hydroxystearic acid or behenic acid, ring opening products of olefin epoxides with 12 to 22 carbon atoms with fatty alcohols. Consistency agents and thickeners
Als Konsistenzgeber kommen in erster Linie Fettalkohole oder Hydroxyfettalkohole mit 12 bis 22 und vorzugsweise 16 bis 18 Kohlenstoffatomen und daneben Partialglyceride, Fettsäuren oder Hydroxyfettsäuren in Betracht. Bevorzugt ist eine Kombination dieser Stoffe mit Alkyloligoglucosiden und/oder Fettsäure-N-methylglucamiden gleicher Kettenlänge und/oder Polyglycerinpoly-12-hydroxystearaten. Geeignete Verdickungsmittel sind beispielsweise Aerosil-Typen (hydrophile Kieselsäuren), Polysaccharide, insbesondere Xanthan-Gum, Agar-Agar, Alginate und Tylosen, Carboxymethylcellulose und Hydroxy- ethyl- und Hydroxypropylcellulose, ferner höhermolekulare Polyethylenglycolmono- und - diester von Fettsäuren, Polyacrylate, (z.B. Carbopole® und Pemulen-Typen von Goodrich; Synthalene® von Sigma; Keltrol-Typen von Kelco; Sepigel-Typen von Seppic; Salcare- Typen von Allied Colloids), Polyacrylamide, Polymere, Polyvinylalkohol und Polyvinylpyrro- lidon. Als besonders wirkungsvoll haben sich auch Bentonite, wie z.B. Bentone® Gel VS- 5PC (Rheox) erwiesen, bei dem es sich um eine Mischung aus Cyclopentasiloxan, Disteardimonium Hectorit und Propylencarbonat handelt. Weiter in Frage kommen Tenside, wie beispielsweise ethoxylierte Fettsäureglyceride, Ester von Fettsäuren mit Polyolen wie beispielsweise Pentaerythrit oder Trimethylolpropan, Fettalkoholethoxylate mit eingeengter Homologenverteilung oder Alkyloligoglucoside sowie Elektrolyte wie Kochsalz und Ammoniumchlorid.Suitable consistency agents are primarily fatty alcohols or hydroxy fatty alcohols with 12 to 22 and preferably 16 to 18 carbon atoms and, in addition, partial glycerides, fatty acids or hydroxy fatty acids. A combination of these substances with alkyl oligoglucosides and / or fatty acid N-methylglucamides of the same chain length and / or polyglycerol poly-12-hydroxystearates is preferred. Suitable thickeners are, for example, Aerosil types (hydrophilic silicas), polysaccharides, in particular xanthan gum, agar agar, alginates and tyloses, carboxymethyl cellulose and hydroxyethyl and hydroxypropyl cellulose, and also higher molecular weight polyethylene glycol mono- and diesters of fatty acids, polyacrylates (e.g. Carbopole® and Pemulen types from Goodrich; Synthalene® from Sigma; Keltrol types from Kelco; Sepigel types from Seppic; Salcare types from Allied Colloids), polyacrylamides, polymers, polyvinyl alcohol and polyvinylpyrrolidone. Bentonites, such as e.g. Bentone® Gel VS-5PC (Rheox), which is a mixture of cyclopentasiloxane, disteardimonium hectorite and propylene carbonate. Surfactants such as ethoxylated fatty acid glycerides, esters of fatty acids with polyols such as pentaerythritol or trimethylolpropane, fatty alcohol ethoxylates with a narrow homolog distribution or alkyl oligoglucosides as well as electrolytes such as table salt and ammonium chloride are also suitable.
Überfettungsmittelsuperfatting
Als Überfettungsmittel können Substanzen wie beispielsweise Lanolin und Lecithin sowie polyethoxylierte oder acylierte Lanolin- und Lecithinderivate, Polyolfettsäureester, Monoglyceride und Fettsäurealkanolamide verwendet werden, wobei die letzteren gleichzeitig als Schaumstabilisatoren dienen.Substances such as, for example, lanolin and lecithin and polyethoxylated or acylated lanolin and lecithin derivatives, polyol fatty acid esters, monoglycerides and fatty acid alkanolamides can be used as superfatting agents, the latter simultaneously serving as foam stabilizers.
Stabilisatorenstabilizers
Als Stabilisatoren können Metallsalze von Fettsäuren, wie z.B. Magnesium-, Aluminium- und/oder Zinkstearat bzw. -ricinoleat eingesetzt werden. PolymereMetal salts of fatty acids such as magnesium, aluminum and / or zinc stearate or ricinoleate can be used as stabilizers. polymers
Die bevorzugten Polymere sind die bereits beschriebenen Kationpolymere. Es können jedoch auch weitere PolYmere eingesetzt werden.The preferred polymers are the cation polymers already described. However, other polymers can also be used.
Als anionische, zwitterionische, amphotere und nichtionische Polymere kommen beispielsweise Vinylacetat/Crotonsäure-Copolymere, Vinylpyrrolidon/Vinylacrylat- Copolymere, Vinylacetat/Butylmaleat/ Isobornylacrylat-Copolymere,Anionic, zwitterionic, amphoteric and nonionic polymers are, for example, vinyl acetate / crotonic acid copolymers, vinylpyrrolidone / vinyl acrylate copolymers, vinyl acetate / butyl maleate / isobornyl acrylate copolymers,
Methylvinylether/Maleinsäureanhydrid-Copolymere und deren Ester, unvernetzte und mit Polyolen vernetzte Polyacrylsäuren, Acrylamidopropyltrimethylammoniumchlorid/ Acrylat- Copolymere, Octylacrylamid/Methylmeth-acrylat/tert.Butylaminoethylmethacrylat/2-Methyl vinyl ether / maleic anhydride copolymers and their esters, uncrosslinked and polyols crosslinked polyacrylic acids, acrylamidopropyltrimethylammonium chloride / acrylate copolymers, octylacrylamide / methyl methacrylate / tert-butylaminoethyl methacrylate / 2-
Hydroxypropylmethacrylat-Copolymere, Polyvinylpyrrolidon, Vinylpyrrolidon/Vinylacetat- Copoly-mere, Vinylpyrrolidon/ Dimethylaminoethylmethacrylat/Vinylcaprolactam-Ter- polymere sowie gegebenenfalls derivatisierte Celluloseether und Silicone in Frage. Weitere geeignete Polymere und Verdickungsmittel sind in Cosm.Toil. 108, 95 (1993) aufgeführt.Hydroxypropyl methacrylate copolymers, polyvinylpyrrolidone, vinylpyrrolidone / vinyl acetate copolymers, vinylpyrrolidone / dimethylaminoethyl methacrylate / vinylcaprolactam terpolymers and, if appropriate, derivatized cellulose ethers and silicones. Other suitable polymers and thickeners are in Cosm.Toil. 108, 95 (1993).
Siliconverbindungensilicone compounds
Geeignete Siliconverbindungen sind beispielsweise Dimethylpolysiloxane, Methylphenylpolysiloxane, cyclische Silicone sowie amino-, fettsäure-, alkohol-, polyether-, epoxy-, fluor-, glykosid- und/oder alkylmodifizierte Siliconverbindungen, die bei Raumtemperatur sowohl flüssig als auch harzförmig vorliegen können. Weiterhin geeignet sind Simethicone, bei denen es sich um Mischungen aus Dimethiconen mit einer durchschnittlichen Kettenlänge von 200 bis 300 Dimethylsiloxan-Einheiten und hydrierten Silicaten handelt. Eine detaillierte Übersicht über geeignete flüchtige Silicone findet sich zudem von Todd et al. in Cosm.Toil. 91, 27 (1976).Suitable silicone compounds are, for example, dimethylpolysiloxanes, methylphenylpolysiloxanes, cyclic silicones and amino, fatty acid, alcohol, polyether, epoxy, fluorine, glycoside and / or alkyl-modified silicone compounds, which can be both liquid and resinous at room temperature. Simethicones, which are mixtures of dimethicones with an average chain length of 200 to 300 dimethylsiloxane units and hydrogenated silicates, are also suitable. A detailed overview of suitable volatile silicones can also be found by Todd et al. in Cosm.Toil. 91, 27 (1976).
Biogene WirkstoffeBiogenic agents
Unter biogenen Wirkstoffen sind beispielsweise Tocopherol, Tocopherolacetat, Tocopherolpalmitat, Ascorbinsäure, (Desoxy)Ribonucleinsäure und deren Fragmentierungsprodukte, ß-Glucane, Retinol, Bisabolol, Allantoin, Phytantriol, Panthenol, AHA-Säuren, Aminosäuren, Ceramide, Pseudoceramide, essentielle Öle, Pflanzenextrakte, wie z.B. Prunusextrakt, Bambaranussextrakt und Vitaminkomplexe zu verstehen. FilmbildnerExamples of biogenic active substances include tocopherol, tocopherol acetate, tocopherol palmitate, ascorbic acid, (deoxy) ribonucleic acid and its fragmentation products, ß-glucans, retinol, bisabolol, allantoin, phytantriol, panthenol, AHA acids, amino acids, ceramides, pseudocleamides, extracts of essential oils, essential extracts such as Prunus extract, Bambaranus extract and vitamin complexes. film formers
Gebräuchliche Filmbildner sind beispielsweise Chitosan, mikrokristallines Chitosan, quater- niertes Chitosan, Polyvinylpyrrolidon, Vinylpyrrolidon-Vinylacetat-Copolymerisate, Polymere der Acrylsäurereihe, quaternäre Cellulose-Derivate, Kollagen, Hyaluronsäure bzw. deren Salze und ähnliche Verbindungen.Common film formers are, for example, chitosan, microcrystalline chitosan, quaternized chitosan, polyvinylpyrrolidone, vinylpyrrolidone-vinyl acetate copolymers, polymers of the acrylic acid series, quaternary cellulose derivatives, collagen, hyaluronic acid or its salts and similar compounds.
AntischuppenwirkstoffeAntidandruff agents
Als Antischuppenwirkstoffe kommen Pirocton Olamin (l-Hydroxy-4-methyl-6-(2,4,4- trimythylpentyl)-2-(lH)-pyridinonmonoethanolaminsalz), Baypival® (Climbazole), Ketoconazol®, (4-Acetyl-l-{-4-[2-(2.4-dichlorphenyl) r-2-(lH-imidazol-l-ylmethyl)-l,3- dioxylan-c-4-ylmethoxyphenyl}piperazin, Ketoconazol, Elubiol, Selendisulfid, Schwefel kolloidal, Schwefelpolyehtylenglykolsorbitanmonooleat, Schwefelrizinolpolyehtoxylat, Schwfel-teer Destillate, Salicylsäure (bzw. in Kombination mit Hexachlorophen), Undexy- lensäure Monoethanolamid Sulfosuccinat Na-Salz, Lamepon® UD (Protein- Undecylensäurekondensat), Zinkpyrithion, Aluminiumpyrithion und Magnesiumpyrithion / Dipyrithion-Magnesiumsulfat in Frage.Piroctone olamine (1-hydroxy-4-methyl-6- (2,4,4-trimythylpentyl) -2- (1H) -pyridinone monoethanolamine salt), Baypival® (climbazole), Ketoconazol®, (4-acetyl-l - {- 4- [2- (2.4-dichlorophenyl) r-2- (lH-imidazol-l-ylmethyl) -l, 3-dioxylan-c-4-ylmethoxyphenyl} piperazine, ketoconazole, elubiol, selenium disulfide, sulfur colloidal, Schwefelpolyehtylenglykolsorbitanmonooleat, Schwefelrizinolpolyehtoxylat, Schwfel tar distillate, salicylic acid (or in combination with hexachlorophene), Undexy- lensäure monoethanolamide sulfosuccinate Na salt, Lamepon® UD (protein undecylenic acid condensate), zinc pyrithione, magnesium pyrithione Aluminiumpyrithion and / dipyrithione magnesium sulfate.
Hydrotropehydrotropes
Zur Verbesserung des Fließverhaltens können ferner Hydrotrope, wie beispielsweise Ethanol, Isopropylalkohol, oder Polyole eingesetzt werden. Polyole, die hier in Betracht kommen, besitzen vorzugsweise 2 bis 15 Kohlenstoffatome und mindestens zwei Hydroxylgruppen. Die Polyole können noch weitere funktionelle Gruppen, insbesondere Aminogruppen, enthalten bzw. mit Stickstoff modifiziert sein. Typische Beispiele sindHydrotropes such as ethanol, isopropyl alcohol or polyols can also be used to improve the flow behavior. Polyols that come into consideration here preferably have 2 to 15 carbon atoms and at least two hydroxyl groups. The polyols can also contain further functional groups, in particular amino groups, or be modified with nitrogen. Typical examples are
> Glycerin;> Glycerin;
> Alkylenglycole, wie beispielsweise Ethylenglycol, Diethylenglycol, Propylenglycol, Butylenglycol, Hexylenglycol sowie Polyethylenglycole mit einem durchschnittlichen Molekulargewicht von 100 bis 1.000 Dalton;> Alkylene glycols, such as ethylene glycol, diethylene glycol, propylene glycol, butylene glycol, hexylene glycol and polyethylene glycols with an average molecular weight of 100 to 1,000 daltons;
> technische Oligoglyceringemische mit einem Eigenkondensationsgrad von 1,5 bis 10 wie etwa technische Diglyceringemische mit einem Diglyceringehalt von 40 bis 50 Gew.-%;> technical oligoglycerol mixtures with a degree of self-condensation of 1.5 to 10 such as technical diglycerol mixtures with a diglycerol content of 40 to 50% by weight;
> Methyolverbindungen, wie insbesondere Trimethylolethan, Trimethylolpropan, Trimethylolbutan, Pentaerythrit und Dipentaerythrit;> Methyl compounds, such as in particular trimethylolethane, trimethylolpropane, trimethylolbutane, pentaerythritol and dipentaerythritol;
> Niedrigalkylglucoside, insbesondere solche mit 1 bis 8 Kohlenstoffen im Alkylrest, wie beispielsweise Methyl- und Butylglucosid;> Lower alkyl glucosides, especially those with 1 to 8 carbons in the alkyl radical, such as for example methyl and butyl glucoside;
> Zuckeralkohole mit 5 bis 12 Kohlenstoffatomen, wie beispielsweise Sorbit oder Mannit,> Sugar alcohols with 5 to 12 carbon atoms, such as sorbitol or mannitol,
> Zucker mit 5 bis 12 Kohlenstoffatomen, wie beispielsweise Glucose oder Saccharose;> Sugar with 5 to 12 carbon atoms, such as glucose or sucrose;
> Aminozucker, wie beispielsweise Glucamin;> Aminosugars such as glucamine;
> Dialkoholamine, wie Diethanolamin oder 2-Amino-l,3-propandiol.> Dialcohol amines, such as diethanolamine or 2-amino-l, 3-propanediol.
Konservierungsmittelpreservative
Als Konservierungsmittel eignen sich beispielsweise Phenoxyethanol, Formaldehydlösung, Parabene, Pentandiol oder Sorbinsäure sowie die unter der Bezeichnung Surfacine® bekannten Silberkomplexe und die in Anlage 6, Teil A und B der Kosmetikverordnung aufgeführten weiteren Stoffklassen.Suitable preservatives are, for example, phenoxyethanol, formaldehyde solution, parabens, pentanediol or sorbic acid, as well as the silver complexes known under the name Surfacine® and the other classes of substances listed in Appendix 6, Parts A and B of the Cosmetics Ordinance.
Parfümöle und AromenPerfume oils and flavors
Als Parfümöle seien genannt Gemische aus natürlichen und synthetischen Riechstoffen. Natürliche Riechstoffe sind Extrakte von Blüten (Lilie, Lavendel, Rosen, Jasmin, Neroli, Ylang-Ylang), Stengeln und Blättern (Geranium, Patchouli, Petitgrain), Früchten (Anis, Koriander, Kümmel, Wacholder), Fruchtschalen (Bergamotte, Zitrone, Orangen), Wurzeln (Macis, Angelica, Sellerie, Kardamon, Costus, Iris, Calmus), Hölzern (Pinien-, Sandel-, Guajak-, Zedern-, Rosenholz), Kräutern und Gräsern (Estragon, Lemongras, Salbei, Thymian), Nadeln und Zweigen (Fichte, Tanne, Kiefer, Latschen), Harzen und Balsamen (Galbanum, Elemi, Benzoe, Myrrhe, Olibanum, Opoponax). Weiterhin kommen tierische Rohstoffe in Frage, wie beispielsweise Zibet und Castoreum. Typische synthetische Riechstoffverbindungen sind Produkte vom Typ der Ester, Ether, Aldehyde, Ketone, Alkohole und Kohlenwasserstoffe. Riechstoffverbindungen vom Typ der Ester sind z.B. Benzylacetat, Phenoxyethylisobutyrat, p-tert.-Butylcyclohexylacetat, Linalylacetat, Dimethylbenzylcarbinylacetat, Phenylethylacetat, Linalylbenzoat, Benzylformiat, Ethylmethylphenylglycinat, Allylcyclohexylpropionat, Styrallylpropionat und Benzylsalicylat. Zu den Ethem zählen beispielsweise Benzylethylether, zu den Aldehyden z.B. die linearen Alkanale mit 8 bis 18 Kohlenstoffatomen, Citral, Citronellal, Citronellyloxyacetaldehyd, Cyclamenaldehyd, Hydroxycitronellal, Lilial und Bourgeonal, zu den Ketonen z.B. die Jonone, α-Isomethylionon und Methylcedrylketon, zu den Alkoholen Anethol, Citronellol, Eugenol, Isoeugenol, Geraniol, Linalool, Phenylethylalkohol und Terpineol, zu den Kohlenwasserstoffen gehören hauptsächlich die Terpene und Balsame. Bevorzugt werden jedoch Mischungen verschiedener Riechstoffe verwendet, die gemeinsam eine ansprechende Duftnote erzeugen. Auch ätherische Öle geringerer Flüchtigkeit, die meist als Aromakomponenten verwendet werden, eignen sich als Parfümöle, z.B. Salbeiöl, Kamillenöl, Nelkenöl, Melissenöl, Minzenöl, Zimtblätteröl, Lindenblütenöl, Wacholderbeerenöl, Vetiveröl, Olibanöl, Galbanumöl, Labolanumöl und Lavandinöl. Vorzugsweise werden Bergamotteöl, Dihydromyrcenol, Lilial, Lyral, Citronellol, Phenylethylalkohol, α-Hexylzimtaldehyd, Geraniol, Benzylaceton, Cyclamenaldehyd, Lina- lool, Boisambrene Forte, Ambroxan, Indol, Hedione, Sandelice, Citronenöl, Mandarinenöl,Perfume oils include mixtures of natural and synthetic fragrances. Natural fragrances are extracts of flowers (lily, lavender, roses, jasmine, neroli, ylang-ylang), stems and leaves (geranium, patchouli, petitgrain), fruits (anise, coriander, caraway, juniper), fruit peel (bergamot, lemon, Oranges), roots (mace, angelica, celery, cardamom, costus, iris, calmus), wood (pine, sandal, guaiac, cedar, rosewood), herbs and grasses (tarragon, lemongrass, sage, thyme), Needles and twigs (spruce, fir, pine, mountain pine), resins and balms (galbanum, elemi, benzoin, myrrh, olibanum, opoponax). Animal raw materials, such as civet and castoreum, are also suitable. Typical synthetic fragrance compounds are products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type. Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinylacetate, phenylethyl acetate, linalyl benzoate, benzyl formate, ethyl methylphenyl glycinate, allyl cyclohexyl benzylatepylpropionate, stally. The ethers include, for example, benzyl ethyl ether, the aldehydes, for example, the linear alkanals having 8 to 18 carbon atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamenaldehyde, hydroxycitronellal, lilial and bourgeonal, the ketones, for example, the jonones, α-isomethylionone and methylcedryl ketone, the alcohols Anethol, citronellol, eugenol, isoeugenol, geraniol, linalool, phenylethyl alcohol and terpineol, the hydrocarbons mainly include the terpenes and balsams. However, preference is given to using mixtures of different fragrances which together produce an appealing fragrance. Also essential oils of lower volatility, most of the time are used as aroma components, are suitable as perfume oils, for example sage oil, chamomile oil, clove oil, lemon balm oil, mint oil, cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, oliban oil, galbanum oil, labolanum oil and lavandin oil. Bergamot oil, dihydromyrcenol, lilial, lyral, citronellol, phenylethyl alcohol, α-hexylcinnamaldehyde, geraniol, benzylacetone, cyclamenaldehyde, linolool, boisambrene forte, ambroxan, indole, hedione, sandelice, lemon oil, mandarin oil, are preferably used.
Orangenöl, Allylamylglycolat, Cyclovertal, Lavandinöl, Muskateller Salbeiöl, ß-Damascone, Geraniumöl Bourbon, Cydohexylsalicylat, Vertofix Coeur, Iso-E-Super, Fixolide NP, Evernyl, Iraldein gamma, Phenylessigsäure, Geranylacetat, Benzylacetat, Rosenoxid, Romilllat, Irotyl und Floramat allein oder in Mischungen, eingesetzt.Orange oil, allylamylglycolate, cyclovertal, lavandin oil, muscatel sage oil, ß-damascone, geranium oil bourbon, cydohexylsalicylate, Vertofix Coeur, Iso-E-Super, Fixolide NP, evernyl, iraldein gamma, phenylacetic acid, geranyl acetate, benzotyl acetate, rose oxylacetate, rose oxylacetate, rose oxylacetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose ethyl acetate, rose gold acetate used alone or in mixtures.
Als Aromen kommen beispielsweise Pfefferminzöl, Krauseminzöl, Anisöl, Sternanisöl, Kümmelöl, Eukalyptusöl, Fenchelöl, Citronenöl, Wintergrünöl, Nelkenöl, Menthol und dergleichen in Frage.Suitable flavors are, for example, peppermint oil, spearmint oil, anise oil, star anise oil, caraway oil, eucalyptus oil, fennel oil, lemon oil, wintergreen oil, clove oil, menthol and the like.
Farbstoffedyes
Als Farbstoffe können die für kosmetische Zwecke geeigneten und zugelassenen Substanzen verwendet werden, wie sie beispielsweise in der Publikation "Kosmetische Färbemittel" der Farbstoffkommission der Deutschen Forschungsgemeinschaft, Verlag Chemie, Weinheim, 1984, S.81-106 zusammengestellt sind. Beispiele sind Kochenillerot A (C.I. 16255), Patentblau V (C.I.42051), Indigotin (C.I.73015), Chlorophyllin (C.I.75810), Chinolingelb (C.I.47005), Titandioxid (C.I.77891), Indanthrenblau RS (C.I. 69800) und Krapplack (C.I.58000). Als Lumineszenzfarbstoff kann auch Luminol enthalten sein. Diese Farbstoffe werden üblicherweise in Konzentrationen von 0,001 bis 0,1 Gew.-%, bezogen auf die gesamte Mischung, eingesetzt. The dyes which can be used are those substances which are suitable and approved for cosmetic purposes, as compiled, for example, in the publication "Cosmetic Dyes" by the Dye Commission of the German Research Foundation, Verlag Chemie, Weinheim, 1984, pp. 81-106. Examples are culinary red A (CI 16255), patent blue V (CI42051), indigotine (CI73015), chlorophyllin (CI75810), quinoline yellow (CI47005), titanium dioxide (CI77891), indanthrene blue RS (CI 69800) and madder varnish (CI58000). Luminol may also be present as the luminescent dye. These dyes are usually used in concentrations of 0.001 to 0.1% by weight, based on the mixture as a whole.
BeispieleExamples
Ölduschbad mit SojaölOil shower bath with soybean oil
Figure imgf000021_0001
Figure imgf000021_0001
Herstellung:production:
Die Herstellung erfolgt bei Raumtemperatur. Alle Substanzen werden zusammen homogen vermischt. The production takes place at room temperature. All substances are mixed together homogeneously.

Claims

Patentansprüche claims
1. Tensidhaltige Waschzubereitungen, enthaltend1. Washing preparations containing surfactant, containing
mindestens 25 Gew.% eines Pflanzenölesat least 25% by weight of a vegetable oil
2. Waschzubereitungen nach Anspruch 1, dadurch gekennzeichnet, dass sie als Tenside nichtionische und/oder anionische und/oder kationische und/oder amphotere und/oder zwitterionische Tenside enthalten.2. Washing preparations according to claim 1, characterized in that they contain nonionic and / or anionic and / or cationic and / or amphoteric and / or zwitterionic surfactants as surfactants.
3. Waschzubereitungen nach den Ansprüchen 1 und/oder 2, dadurch gekennzeichnet, dass sie als nichtionische Tenside Alkyl- und/oder Alkenyloligoglykoside der Formel (I) enthalten,3. washing preparations according to claims 1 and / or 2, characterized in that they contain alkyl and / or alkenyl oligoglycosides of the formula (I) as nonionic surfactants,
Figure imgf000022_0001
Figure imgf000022_0001
in der R1 für einen Alkyl- und/oder Alkenylrest mit 4 bis 22 Kohlenstoffatomen, G für einen Zuckerrest mit 5 oder 6 Kohlenstoffatomen und p für Zahlen von 1 bis 10 steht.in which R 1 is an alkyl and / or alkenyl radical having 4 to 22 carbon atoms, G is a sugar radical having 5 or 6 carbon atoms and p is a number from 1 to 10.
4. Waschzubereitungen nach mindestens einem der Ansprüche 1 bis 3, dadurch gekennzeichnet, dass sie als amphotere Tenside Betaine und/oder Amphoacetate enthalten.4. Washing preparations according to at least one of claims 1 to 3, characterized in that they contain betaines and / or amphoacetates as amphoteric surfactants.
5. Waschzubereitungen nach mindestens einem der Ansprüche 1 bis 4, dadurch gekennzeichnet, dass sie als weitere Komponente Kationpolymere enthalten.5. washing preparations according to at least one of claims 1 to 4, characterized in that they contain cation polymers as a further component.
6. Waschzubereitungen nach mindestens einem der Ansprüche 1 bis 5, dadurch gekennzeichnet, dass sie Wachsdispersionen enthalten.6. washing preparations according to at least one of claims 1 to 5, characterized in that they contain wax dispersions.
7. Waschzubereitungen nach mindestens einem der Ansprüche 1 bis 6, dadurch gekennzeichnet, dass sie maximal 55 Gew.% Wasser enthalten.7. Washing preparations according to at least one of claims 1 to 6, characterized in that they contain a maximum of 55% by weight of water.
8. Waschzubereitungen nach mindestens einem der Ansprüche 1 bis 7, dadurch gekennzeichnet, dass sie Pflanzenöle enthalten, ausgewählt aus der Gruppe, die gebildet wird von Sojaöl, Mandelöl, Jojobaöl, Olivenöl, Sonnenblumenkernöl, Sesamöl, Nachtkerzenöl, Distelöl und Weizenkeimöl. 8. washing preparations according to at least one of claims 1 to 7, characterized in that they contain vegetable oils selected from the group consisting of soybean oil, almond oil, jojoba oil, olive oil, sunflower seed oil, sesame oil, evening primrose oil, safflower oil and wheat germ oil.
. Waschzubereitungen nach mindestens einem der Ansprüche 1 bis 8, dadurch gekennzeichnet, dass sie, Washing preparations according to at least one of claims 1 to 8, characterized in that they
(a) mindestens 25 Gew. % Pflanzenöle,(a) at least 25% by weight of vegetable oils,
(b) 0,5 bis 20 Gew.-% Alkyl- und/oder Alkenyloligoglykoside,(b) 0.5 to 20% by weight of alkyl and / or alkenyl oligoglycosides,
(c) 0,5 bis 30 Gew.-% amphotere Tenside,(c) 0.5 to 30% by weight of amphoteric surfactants,
(d) 0 bis 5 Gew.-% Kationpolymere mit der Maßgabe enthalten, dass sich die Angaben mit Wasser und weiteren üblichen Hilfs- und Zusatzstoffen zu 100 Gew.-% addieren.(d) 0 to 5% by weight of cation polymers with the proviso that the information with water and other conventional auxiliaries and additives add up to 100% by weight.
10. Verwendung von Mischungen, enthaltend Alkyl- und/oder Alkenyloligoglykoside, amphotere Tenside und gegebenenfalls Kationpolymere zur Herstellung von Waschzubereitungen mit mindestens 25 Gew. % Pflanzenölen. 10. Use of mixtures containing alkyl and / or alkenyl oligoglycosides, amphoteric surfactants and optionally cation polymers for the production of washing preparations with at least 25% by weight of vegetable oils.
PCT/EP2003/000908 2002-02-08 2003-01-30 Washing preparations with vegetable oils WO2003066017A1 (en)

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FR2956975A1 (en) * 2010-03-03 2011-09-09 Rhodia Operations NEW AGENT TO IMPROVE OIL DEPOSITION ON HAIR
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WO2009071945A2 (en) * 2007-12-03 2009-06-11 Neal's Yard (Natural Remedies) Ltd Skin and hair wash preparation
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