WO2003079794A1 - Use of olive tree extracts in detergents, rinsing agents and cleaning agents - Google Patents
Use of olive tree extracts in detergents, rinsing agents and cleaning agents Download PDFInfo
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- WO2003079794A1 WO2003079794A1 PCT/EP2003/002569 EP0302569W WO03079794A1 WO 2003079794 A1 WO2003079794 A1 WO 2003079794A1 EP 0302569 W EP0302569 W EP 0302569W WO 03079794 A1 WO03079794 A1 WO 03079794A1
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- oil
- extracts
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q17/00—Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
- A61Q17/005—Antimicrobial preparations
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N65/00—Biocides, pest repellants or attractants, or plant growth regulators containing material from algae, lichens, bryophyta, multi-cellular fungi or plants, or extracts thereof
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K8/00—Cosmetics or similar toiletry preparations
- A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
- A61K8/96—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution
- A61K8/97—Cosmetics or similar toiletry preparations characterised by the composition containing materials, or derivatives thereof of undetermined constitution from algae, fungi, lichens or plants; from derivatives thereof
- A61K8/9783—Angiosperms [Magnoliophyta]
- A61K8/9789—Magnoliopsida [dicotyledons]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61Q—SPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
- A61Q19/00—Preparations for care of the skin
- A61Q19/10—Washing or bathing preparations
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/382—Vegetable products, e.g. soya meal, wood flour, sawdust
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/48—Medical, disinfecting agents, disinfecting, antibacterial, germicidal or antimicrobial compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/22—Organic compounds
- C11D7/40—Products in which the composition is not well defined
- C11D7/44—Vegetable products
Definitions
- the invention is in the field of cleaning agents and relates to the use of extracts from the olive tree as an antimicrobial active ingredient in detergents, dishwashing detergents and cleaning agents.
- the object of the present invention is therefore to provide new antimicrobial active ingredients which on the one hand are notable for good activity, but on the other hand also have excellent dermatological tolerance and a low risk of allergy. These active ingredients should be easy to process in washing formulations and should have good compatibility with other auxiliaries. Description of the invention
- the invention relates to the use of extracts from the olive tree as an antimicrobial active ingredient in detergents, dishwashing detergents and cleaning agents.
- extracts from the olive tree in particular from the leaves of the olive tree and / or from the wastewater from olive oil production, have an antimicrobial action against aerobic, anaerobic germs, yeasts and molds. They can be easily incorporated into formulations with a high proportion of surfactants without losing their effectiveness and are characterized by very good dermatological compatibility.
- the extracts to be used according to the invention are prepared by customary extraction methods.
- suitable conventional extraction methods such as maceration, remaceration, digestion, movement maceration, vortex extraction, ultrasound extraction, countercurrent extraction, percolation, repercolation, evacolation (extraction under reduced pressure), diacolation and solid-liquid extraction under continuous reflux , which is carried out in a Soxhiet extractor, which is familiar to a person skilled in the art and in principle all can be used, is exemplary of Hager's Handbook of Pharmaceutical Practice, (5th edition, vol. 2, pp. 1026-1030, Springer Verlag, Berlin- Heidelberg-New-York 1991). Fresh or dried parts of the olive tree can be used as the starting material, but usually leaves are used which are mechanically shredded before extraction. All grinding methods known to the person skilled in the art are suitable here, for example crushing with a mortar.
- the extraction is usually carried out at 20 to 100 ° C, preferably at 20 to 85 ° C, in particular either at the boiling point of the solvent used or at room temperature.
- the extraction takes place under an inert gas atmosphere to avoid oxidation of the ingredients of the extract.
- the extraction times are set by the person skilled in the art depending on the starting material, the extraction process, the extraction temperature, the ratio of solvent to raw material, etc.
- the crude extracts obtained can optionally be subjected to further customary steps, such as purification, concentration and / or decolorization. If desired, the extracts produced in this way can, for example, be subjected to a selective separation of individual undesirable ingredients.
- the extraction can be carried out to any desired degree of extraction, but is usually carried out until exhaustion.
- the present invention includes the knowledge that the extraction conditions and the yields of the final extracts can be selected depending on the desired field of use. If desired, the extracts can then be subjected to spray drying or freeze drying, for example.
- the amount of the extracts used in the preparations mentioned depends on the type of application of the extracts and on the concentration of the individual ingredients.
- the total amount of the olive tree leaf extract which is contained in the preparations according to the invention is generally 0.01 to 15% by weight, preferably 0.05 to 5% by weight, in particular 0.1 to 3% by weight, based on the final preparation, with the proviso that the quantities with water and possibly other auxiliary substances and additives add up to 100% by weight.
- Olive tree leaf extracts are preferably used, which are standardized with regard to their main ingredient oleuropein. They contain 1 to 40% by weight, preferably 5 to 30% by weight, particularly preferably 10 to 25% by weight and especially 18 to 22% by weight oleuropein, based on the dry extract.
- Extracts from the wastewater of olive tree production are produced by drying the water, preferably by spray drying, after addition of auxiliaries such as mannitol or sodium caseinate. They are adjusted to a content of polyphenols, preferably hydroxytyrosol and tyrosol, which is at least 0.5% by weight, preferably at least 1% by weight and particularly preferably at least 2% by weight, based on the dry extract.
- Active substance in the sense of the invention relates to the proportion of substances and auxiliaries and additives which are contained in the preparations, with the exception of the additionally added water.
- Another object of the invention are washing, rinsing or cleaning agent preparations containing extracts from the leaves of the olive tree and / or from the wastewater of olive oil production and at least 10% by weight, preferably at least 15% by weight and particularly preferably at least 20% by weight .% of active substance of an anionic and / or cationic and / or amphoteric and / or nonionic surfactant - based on the preparation.
- the present invention also relates to the use of the olive tree extracts for the production of washing, rinsing and cleaning agents.
- Common detergents, dishwashing detergents and cleaning agents contain - based on the preparation - for example 0.01 to 15% by weight of extracts from the leaves of the olive tree and / or from the wastewater of olive oil production and at least 10% by weight of active substance of an anionic and / or cationic and / or amphoteric and / or nonionic surfactants, preferably they contain 0.05 to 5% by weight of extracts from the leaves of the olive tree and / or from the wastewater from olive oil production and at least 15% by weight of active substance of an anionic and / or cationic and / or amphoteric and / or nonionic surfactants, and particularly preferably 0.1 to 3% by weight of extracts from the leaves of the olive tree and / or from the waste water from olive oil production and at least 20% by weight of active substance of an anionic and / or cationic and / or amphoteric and / or nonionic surfactants.
- the extracts are preferably used in hand dishwashing detergents and body detergents.
- the hand dishwashing detergents according to the invention preferably contain alk (en) yl oligoglycosides as surfactants.
- alkyl and alkenyl oligoglycosides preferably contained in the hand dishwashing detergents follow the formula (I) R 0- [G] P (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. They can be obtained according to the relevant procedures in preparative organic chemistry.
- 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 olomerization (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 is 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, alaidyl alcohol, petroselinyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol, brassidyl alcohol and their technical mixtures, which can be obtained as well as their technical mixtures.
- Alkyl oligoglucosides based on hydrogenated Ci2 / i4 coconut alcohol with a DP of 1 to 3 are preferred.
- the hand dishwashing detergents according to the invention can contain further nonionic surfactants.
- nonionic surfactants are alkoxylated carboxylic acid esters, hydroxy mixed ethers, fatty alcohol polyglycol ethers, alkylphenol polyglycol ether, fatty acid amide polyglycol ether, fatty amine polyglycol ether, alkoxylated triglycerides, fatty acid N-alkyl-glucamides, protein hydrolysates (especially vegetable products based on wheat), polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides.
- the nonionic surfactants contain polyglycol ether chains, they can have a conventional, but preferably a narrow, homolog distribution.
- nonionic surfactants are preferably selected from the group formed by alkoxylated carboxylic acid esters, hydroxy mixed ethers, fatty alcohol polyglycol ethers, end group-capped fatty alcohol polyglycol ethers, amine oxides and fatty acid N-alkyl glucamides.
- the agents according to the invention can contain anionic surfactants.
- anionic surfactants are soaps, alkyl benzene sulfonates, alkane sulfonates, olefin sulfonates, alkyl ether sulfonates, glycerol ether sulfonates, ⁇ -methyl ester sulfonates, sulfo fatty acids, alkyl and / or alkenyl sulfates, alkyl ether sulfates, glycerol ether sulfates, fatty acid monoglyid sulfate (ether sulfate amide), monoglyid sulfate (ether) ether) sulfates, mono- and dialkylsulfosuccinates, mono- and dialkylsulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts,
- the hand dishwashing detergents according to the invention contain amphoteric or zwitterionic surfactants.
- amphoteric or zwitterionic surfactants are alkyl betaines, alkyl amido betaines, aminopropionates, imidazolinium betaines and sulfobetaines.
- Betaines are known surfactants which are predominantly produced by carboxyalkylation, preferably carboxymethylation, of aminic compounds.
- the starting materials are preferably contacted with halocarboxylic acids or their salts, in particular with sodium chloroacetate. dense, forming one mole of salt per mole of betaine.
- unsaturated carboxylic acids such as acrylic acid, is also possible.
- Optional auxiliary agents such as builders, e.g. Glutaric acid, succinic acid, adipic acid, tartaric acid, gluconic acid, trisodium citrate, solvents, e.g. Acetone or ethanol, hydrotrope e.g. Cumene sulfonate, butyl glucoside, butylene glycol, viscosity regulators such as Fatty acid alkanolamides, pH regulators, e.g. Citric acid, caustic soda and potassium hydroxide, pearlescent agents such as Stearic acid derivatives. It can also contain dyes and fragrances.
- builders e.g. Glutaric acid, succinic acid, adipic acid, tartaric acid, gluconic acid, trisodium citrate
- solvents e.g. Acetone or ethanol
- hydrotrope e.g. Cumene sulfonate
- butyl glucoside butylene glycol
- viscosity regulators such
- the hand dishwashing detergents can of course contain other antimicrobial active ingredients. Quaternized ammonium compounds, quaternized fatty acid triethanolamine ester salts (esterquats) and / or aromatic alcohols are preferably used for this purpose.
- fragrance compounds for example the synthetic products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type, can be used as perfume oils or fragrances.
- Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert.-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinyl acetate, phenylethyl acetate, linalyl benzoate, benzyl formate, ethyl methylphenylglycinate, allylcyclohexyl benzylatepylpropionate, stally.
- the ethers include, for example, benzyl ethyl ether, the aldehydes, for example, the linear alkanals with 8-18 C atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamenaldehyde, hydroxycitronellal, lilial and bourgeonal, and the ketones include, for example, the jonones, ⁇ -isomethylionone and methylcedrylke - clay, the alcohols anethole, citronellol, eugenol, geraniol, linalool, phenylethyl alcohol and terpinol, the hydrocarbons mainly include the terpenes such as limonene and pinene.
- Perfume oils of this type can also contain natural fragrance mixtures such as are obtainable from plant sources, for example pine, citrus, jasmine, patchouly, rose or ylang-ylang oil. Also suitable are muscatel, sage oil, chamomile oil, clove oil, lemon balm oil, mint oil, cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, olibanum oil, galbanum oil and labdanum oil as well as orange blossom oil, neroliol, orange peel oil and sandalwood oil. body wash
- the body detergents according to the invention can be present as hair shampoos, foam baths, shower baths, washing lotions or bars of soap. These agents can also be used as further auxiliaries and additives, mild surfactants, oil bodies, emulators, pearlescent waxes, consistency agents, thickeners, superfatting agents, stabilizers, polymers, silicone compounds, fats, waxes, lecithins, phospholipids, biogenic active ingredients, antidandruff agents, film formers, hydrotropes, Contain solubilizers, preservatives, perfume oils, dyes and the like.
- Anionic, nonionic, cationic and / or amphoteric or zwitterionic surfactants may be present as surface-active substances, the proportion of which in the compositions is usually about 1 to 70, preferably 5 to 50 and in particular 10 to 30% by weight.
- anionic surfactants are soaps, alkyl benzene sulfonates, alkane sulfonates, olefin sulfonates, alkyl ether sulfonates, glycerol ether sulfonates, ⁇ -methyl ester sulfonates, sulfo fatty acids, alkyl sulfates, fatty alcohol ether sulfates, glycerol ether sulfates, fatty acid ether sulfates, ether ether sulfates (mono) ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, mono ether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether 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, alkylphenol 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 (especially glucoronic acid derivatives) Wheat-based products), 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.
- cationic surfactants are quaternary ammonium compounds, such as, for example, dimethyldistearylammonium chloride, and esterquats, in particular quaternized fatty acid trialkanolamine ester salts.
- amphoteric or zwitterionic surfactants are alkyl betaines, alkyl amido betaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines. The surfactants mentioned are exclusively known compounds.
- Typical examples of particularly suitable mild, ie particularly skin-compatible surfactants are fatty alcohol polyglycol ether sulfates, monoglyceride sulfates, mono- and / or dialkyl sulfosuccinates, fatty acid isethio nates, fatty acid sarcosinates, fatty acid taurides, fatty acid glutamates, ⁇ -olefin sulfonates, ether carboxylic acids, alkyl oligoglucosides, fatty acid glucamides, alkyl amido betaines, amphoacetals and / or protein fatty acid condensates, the latter preferably based on wheat proteins.
- esters of linear C6-C22 fatty acids with branched alcohols in particular 2-ethylhexanol
- esters of linear and / or branched fatty acids are also suitable polyhydric alcohols (such as propylene glycol, dimer diol or trimer triol) and / or Guerbet alcohols, triglycerides based on C6-C ⁇ o fatty acids, liquid mono- / di- / triglyceride mixtures based on C ⁇ -Cis fatty acids, esters of C6-C22- Fatty alcohols and / or Guerbet alcohols with aromatic carboxylic acids, especially benzoic acid, esters of C2-Ci2-dicarboxylic acids with linear or branched alcohols with 1 to 22 carbon atoms or polyols with 2 to 10
- 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.
- Suitable emulsifiers are nonionic surfactants from at least one of the following groups:
- Partial esters of polyglycerol (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 (e.g. cellulose) / or 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; Polymer emulsifiers, e.g. Pemulen types (TR-1, TR-2) from Goodrich;
- adducts of ethylene oxide and / or of propylene oxide with fatty alcohols, fatty acids, alkylphenols or with castor oil are known, commercially available products are homolog mixtures whose average degree of alkoxylation corresponds to the ratio of the amounts of ethylene oxide and / or propylene oxide and substrate with which the addition reaction is carried out.
- Ci2 / ⁇ s fatty acid monoesters and diesters of adducts of ethylene oxide with glycerol are known as refatting agents for cosmetic preparations.
- Alkyl and / or alkenylollgoglycosides their preparation and their use are known from the prior art. They are produced in particular by reacting glucose or oligosaccharides with primary alcohols with 8 to 18 carbon atoms.
- glycoside residue both monoglycosides in which a cyclic sugar residue is glycosidically bound to the fatty alcohol and oligomeric glycosides with a degree of oligomerization of up to about 8 are suitable.
- the degree of olomerization is a statistical mean value which is based on a homolog distribution customary for such technical products.
- Suitable partial glycerides are hydroxystearic acid monoglyceride, stearic acid diglyceride hydroxy, isostearic acid, Isostearinklarediglycerid, ⁇ lklaremonogly- cerid, oleic acid diglyceride, Ricinolklaremoglycerid, Ricinolklarediglycerid, Linolklaremonoglycerid, Linolklarediglycerid, Linolenchuremonoglycerid, Linolenchurediglycerid, Erucaklaklamonoglycerid, Erucaklakladiglycerid, Weinchuremonoglycerid, Weinklarediglycerid, Citronenklamonoglycerid, Citronendiglycerid, ⁇ pfelklamonoglycerid, 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
- sorbitan sorbitan, sorbitan sesquiisostearate, sorbitan come diisostearate, sorbitan triisostearate, sorbitan monooleate, sorbitan dioleate, bitantrioleat sorting, Sorbitanmonoerucat, Sorbitansesquierucat, Sorbitandierucat, Sorbitantrierucat, sorting bitanmonoricinoleat, Sorbitansesquiricinoleat, Sorbitandiricinoleat, Sorbitantriricinoleat, sorbitan monohydroxystearat, Sorbitansesquihydroxystearat, Sorbitandihydroxystearat , Sorbitan trihydroxystearate, sorbitan monotartrate, sorbitan sesq u i-tartrate, sorbitan ditartrate, sorbitan tritartrate, sorbi- Tan monocitrate, sorbitan sesquicitrate, sorbitan
- polyglycerol esters are polyglyceryl-2 dipolyhydroxystearates (Dehymuls® PGPH), polyglycerol-3-diisostearates (Lameform® TGI), polyglyceryl-4 isostearates (Isolan® Gl 34), polyglyceryl-3 oleates, diisostearoyl polyglyceryl polyglyceryl 3 diisostearates (Isolan® PDI), polyglyceryl-3 methylglucose distearate (Tego Care® 450), polyglyceryl-3 beeswax (Gera 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-2 dipo
- 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.
- Zwitterionic surfactants can also be used as emulsifiers.
- Zwitterionic surfactants are surface-active compounds that contain at least one quaternary ammonium group and at least one carboxylate and one sulfonate group in the molecule.
- Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example coconut alkyldimethylammonium glycinate, N-acylaminopropyl-N, N-dimethylammonium glycinate, for example coconut acylaminopropyldimethylammonium glycinate, and 2-alkyl-3 -carboxylmethyl-3-hydroxyethylimidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and the coconut acylaminoethyl hydroxyethylcarboxymethylglycinate.
- betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example coconut alkyldimethylammonium glycinate, N-acylaminopropyl-N, N-dimethylammonium glycinate
- Suitable emulsifiers are ampholytic surfactants.
- Ampholytic surfactants are surface-active compounds which, in addition to a Cs-alkyl or acyl group, contain at least one free amino group and at least one -COOH or -S ⁇ 3H group in the molecule and are capable of forming internal salts.
- ampholytic surfactants are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids, each with about 8 to 18 carbon atoms in the alkyl group.
- Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, cocacylaminoethylaminopropionate and Ci2 / i8-acylsarcosine.
- cationic surfactants are also suitable as emulsifiers, those of the esterquat type, preferably methyl-quaternized difatty acid triethanolamine ester salts, being particularly preferred.
- Typical examples of fats are glycerides, i.e. Solid or liquid vegetable or animal products, which consist essentially of mixed glycerol esters of higher fatty acids, come as waxes, among others. natural waxes, e.g. Candelilla wax, carnauba wax, japan wax, esparto grass wax, cork wax, guaruma wax, rice germ oil wax, sugar cane wax, ouricury wax, montan wax, beeswax, shellac wax, walnut, lanolin (wool wax), pretzel fat, ceresin, ozokerite (earth wax), petrolatum, paraffin waxes, micro waxes chemically modified waxes (hard waxes), e.g.
- natural waxes e.g. Candelilla wax, carnauba wax, japan wax, esparto grass wax, cork wax, guaruma wax, rice germ oil wax, sugar cane wax, ouricury wax, montan wax
- lecithins is understood by the person skilled in the art to mean those glycerophospholipids which form from fatty acids, glycerol, phosphoric acid and choline by esterification. Lecithins are therefore often used in the professional world as phosphatidylcholines (PC).
- PC phosphatidylcholines
- Examples of natural lecithins are the cephalins, which are also referred to as phosphatidic acids and are derivatives of 1,2-diacyl-sn-glycerol-3-phosphoric acids.
- phospholipids are usually understood to be mono- and preferably diesters of phosphoric acid with glycerol (glycerol phosphates), which are generally classed as fats.
- glycerol phosphates glycerol phosphates
- sphingosines or sphingolipids are also suitable.
- Pearlescent waxes that can be used are, for example: Al ky leng lycolester, especially ethylene glycol distearate; Fatty acid alkanolamides, especially coconut fatty acid diethanolamide; Partial glycerides, especially steak rinklamonoglycerid; 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 with 12 to 22 carbon atoms and / or polyols
- Suitable consistency agents are primarily fatty alcohols or hydroxyfatty alcohols with 12 to 22 and preferably 16 to 18 carbon atoms and also partial glycerides, fatty acids or hydroxyfatty acids. A combination of these substances with alkylollgoglucosides 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, guar guar, 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, (eg 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 Poly vinyl pyrrolidone.
- Aerosil types hydrophilic silicas
- polysaccharides in particular xanthan gum, guar guar, agar agar, alginates and tyloses, carboxymethyl cellulose and hydroxyethyl and hydroxypropyl cellulose,
- 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.
- Substances such as, for example, lanolin and lecithin, and also 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. stabilizers
- Metal salts of fatty acids such as e.g. Magnesium, aluminum and / or zinc stearate or ricinoleate are used.
- Suitable cationic polymers are, for example, cationic cellulose derivatives, e.g. a quaternized hydroxyethyl cellulose available under the name Polymer JR 400® from Amerchol, cationic starch, copolymers of diallylammonium salts and acrylamides, quaternized vinylpyrrolidone / vinylimidazole polymers such as e.g.
- Luviquat® condensation products of polyglycols and amines, quaternized collagen polypeptides, such as lauryldimonium hydroxypropyl hydrolyzed collagen (Lamequat®L / Grünau), quaternized wheat polypeptides, polyethyleneimine, cationic silicone polymers, such as e.g.
- Amodimethicones, copolymers of adipic acid and dimethylaminohydroxypropyldiethylenetriamine (Cartaretine® / Sandoz), copolymers of acrylic acid with dimethyldiallylammonium chloride (Merquat® 550 / Chemviron), polyaminopolyamides, as well as their crosslinked water-soluble polymers, cationic chitin derivatives, such as quanernized, optionally quaternized, Condensation products from dihaloalkylene, such as Dibromobutane with bisdialkylamines, e.g. Bis-dimethylamino-1,3-propane, cationic guar gum, e.g. Jaguar® CBS, Jaguar® C-17, Jaguar® C-16 from Celanese, quaternized ammonium salt polymers, e.g. Mirapol® A-15, Mirapol® AD-1, Mirapol® AZ-1 from Miranol.
- Anionic, zwitterionic, amphoteric and nonionic polymers include, for example, vinyl acetate / crotonic acid copolymers, vinylpyrrolidone / vinyl acrylate copolymers, vinyl acetate / butyl maleate / isobomylacrylate copolymers, methyl vinyl ether / maleic anhydride copolymers and their crosslinked polyols and their esters, polyols and their polyols , Acrylamidopropyltrimethylammonium chloride / acrylate copolymers, octylacrylamide / methyl methacrylate / tert.butylaminoethyl methacrylate / 2-hydroxypropyl methacrylate copolymers, polyvinylpyrrolidone, vinylpyrrolidone / vinyl acetate copolymers, vinylpyrrolidone / dimethylamino-methyl-acrylate and acrylate-vinyl
- 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 are both liquid and resinous at room temperature. can lie.
- Simethicones which are mixtures of dimethicones with an average chain length of 200 to 300 dimethylsiloxane units and hydrogenated silicates, are also suitable.
- biogenic active substances are 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, pseudo-leeroceramides, essential extracts, plant extracts Understand vitamin complexes.
- 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-1, 3-propanediol. preservative
- 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 Regulation.
- 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 methylphenylglycinate, allylcyclohexyl benzylatepylpropionate, allyl cyclohexyl propyl pionate.
- the ethers include, for example, benzyl ethyl ether
- the aldehydes include, for example, the linear alkanals having 8 to 18 carbon atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamenaldehyde, hydroxycitronellal, lilial and bourgeonal
- the ketones include, for example, the jonones, ⁇ -isomethylionone and methylcedryl ketone the alcohols anethole, citronellol, eugenol, isoeugenol, geraniol, linalool, phenylethyl alcohol and terpineol
- the hydrocarbons mainly include the terpenes and balsams.
- fragrance oils of lower volatility which are mostly used as aroma components, are also 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 which are suitable and approved for cosmetic purposes. Examples are Kochillerot A (Cl 16255), patent blue V (C.1.42051), indigotine (C.1.73015), chlorophylline (C.1.75810), quinoline yellow (CI47005), titanium dioxide (C.1.77891), indanthrene blue RS (Cl 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 total proportion of auxiliaries and additives can be 1 to 50, preferably 5 to 40,% by weight, based on the composition.
- the agents can be produced by customary cold or hot processes; the phase inversion temperature method is preferably used.
- Leaves of the olive tree (Olea europaea) were collected, dried, ground and extracted by a 55-60 vol.% Ethanol / water mixture at 60 ° C. for 4 hours. The eluate was dried, ground and sieved and adjusted to a content of approximately 20% by weight oleuropein.
- test germs were subcultured on Columbia blood agar (bioMerieux Art. 43049). Sufficient colonies were homogenized in NaCl peptone buffer using a swab so that the turbidity corresponded to the McFarland Standard 1.0.
- test germs were subcultured on Schaedler agar (bioMerieux Art. 43273). Sufficient colonies were homogenized in NaCl peptone buffer using a swab so that the turbidity corresponded to the McFarland Standard 1.0.
- test germs were subcultured on Sabouraud agar HLT (Merck, Art. 18364). Sufficient colonies were homogenized in NaCl peptone buffer using a swab so that the turbidity corresponded to the McFarland Standard 1.0.
- a test concentration of 5% by weight of olive tree leaf extract (Herbalia®Olive - Cognis Iberia SL, Poligono San Vicente, 08755 Castellbisbal, Barcelona (Spain)) was obtained by weighing out 0.5 g of dry extract and dissolving to 10 ml with 15% by volume of ethanol ( Merck, Art. 100971). controls:
- test plates were created for each batch.
- the agar plates were
- test germs were homogenized 2% with the appropriate test medium (see below). 15 ml of this was poured into petri dishes.
- the microorganisms from the olive tree leaf extract are significantly inhibited.
- Staphylococcus epidermidis is subject to inhibition even at very low sample concentrations.
- Table 2 below contains a number of formulation examples with olive tree leaf extract as an antimicrobial agent.
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Abstract
Description
Verwendung von Extrakten des Olivenbaumes in Wasch-, Spül- und ReinigungsmittelnUse of extracts from the olive tree in detergents, dishwashing detergents and cleaning agents
Die Erfindung befindet sich auf dem Gebiet der Reinigungsmittel und betrifft die Verwendung von Extrakten des Olivenbaumes als antimikrobiellen Wirkstoff in Wasch-, Spül-, und Reingungsmitteln.The invention is in the field of cleaning agents and relates to the use of extracts from the olive tree as an antimicrobial active ingredient in detergents, dishwashing detergents and cleaning agents.
Stand der TechnikState of the art
Die Verwendung von antimikrobiellen Wirkstoffen in Wasch-, Spül- und Reinigungsmitteln ist seit vielen Jahren bekannt. Ihr Einsatz führt jedoch immer wieder zu Problemen.The use of antimicrobial agents in washing, rinsing and cleaning agents has been known for many years. However, their use always leads to problems.
Die Anwender insbesondere von Waschmitteln, mit denen Hautkontakt gegeben ist, klagen über die schlechte dermatologische Verträglichkeit eingesetzter antimikrobieller Wirkstoffe. Die Zahl der Allergien und Hauterkrankungen nimmt stetig zu. Die Entwickler und Formulierer bemängeln die mangelnde Kompatibilität mit anderen Hilfsstoffen. Während die Substanzen einerseits eine ausreichende Wasserlöslichkeit aufweisen sollen, müssen sie andererseits hinreichend lipophil sein, um die Bakterienwand durchdringen zu können. Die Mikrobiologen beklagen die abnehmende antimikrobielle Wirksamkeit dieser Wirkstoffe in Kombination mit anderen Hilfsstoffen in Wach- und Reinigungsmitteln. Auch die zunehmende Resistenzbildung stellt die Wissenschaft vor ein weiteres Problem. Das Anforderungsprofil an antimikrobielle Wirkstoffe in Wasch-, Spül- und Reinigungsmitteln ist daher sehr hoch, so dass ständig nach neuen Wirkstoffen gesucht wird, die dieses in optimaler Weise erfüllen können.Users of detergents in particular, with which there is skin contact, complain about the poor dermatological tolerance of the antimicrobial agents used. The number of allergies and skin diseases is increasing steadily. The developers and formulators criticize the lack of compatibility with other auxiliaries. While on the one hand the substances should have sufficient water solubility, on the other hand they must be sufficiently lipophilic to be able to penetrate the bacterial wall. The microbiologists complain about the diminishing antimicrobial effectiveness of these active substances in combination with other auxiliary substances in detergents and cleaning agents. The increasing development of resistance also poses another problem for science. The profile of requirements for antimicrobial agents in detergents, dishwashing detergents and cleaning agents is therefore very high, so that new agents are constantly being sought that can optimally fulfill them.
Die Aufgabe der vorliegenden Erfindung ist es demnach, neue antimikrobielle Wirkstoffe zur Verfügung zu stellen, die sich einerseits durch eine gute Wirksamkeit, andererseits aber auch eine ausgezeichnete dermatologische Verträglichkeit und ein geringes Allergierisiko auszeichnen. Diese Wirkstoffe sollen sich einfach in Waschformulierungen verarbeiten lassen und eine gute Kompatibilität mit anderen Hilfsstoffen aufweisen. Beschreibung der ErfindungThe object of the present invention is therefore to provide new antimicrobial active ingredients which on the one hand are notable for good activity, but on the other hand also have excellent dermatological tolerance and a low risk of allergy. These active ingredients should be easy to process in washing formulations and should have good compatibility with other auxiliaries. Description of the invention
Gegenstand der Erfindung ist die Verwendung von Extrakten des Olivenbaumes als antimikrobieller Wirkstoff in Wasch-, Spül- und Reinigungsmitteln.The invention relates to the use of extracts from the olive tree as an antimicrobial active ingredient in detergents, dishwashing detergents and cleaning agents.
Es wurde gefunden, dass Extrakte des Olivenbaumes, insbesondere aus den Blättern des Olivenbaumes und/oder aus dem Abwasser der Olivenölherstellung, eine antimikrobielle Wirkung gegen aerobe, anaerobe Keime, Hefen und Schimmelpilze haben. Sie lassen sich leicht in Formulierungen mit einem hohen Anteil an Tensiden einarbeiten ohne ihre Wirksamkeit zu verlieren und zeichnen sich durch eine sehr gute dermatologische Verträglichkeit aus.It has been found that extracts from the olive tree, in particular from the leaves of the olive tree and / or from the wastewater from olive oil production, have an antimicrobial action against aerobic, anaerobic germs, yeasts and molds. They can be easily incorporated into formulations with a high proportion of surfactants without losing their effectiveness and are characterized by very good dermatological compatibility.
Durch diese Eigenschaften eignen sie sich besonders zum Einsatz in Wasch-, Spül- und Reinigungsmitteln. Ihre gute Hautverträglichkeit führt zu einem bevorzugten Einsatz in Körperwaschmitteln oder Reinigungsmitteln, deren Anwendung mit einem direkten Kontakt mit der Haut einhergeht, wie zum Beispiel Handgeschirrspülmitteln.These properties make them particularly suitable for use in detergents, dishwashing detergents and cleaning agents. Their good skin tolerance leads to their preferred use in body detergents or cleaning agents, the use of which is associated with direct contact with the skin, such as hand dishwashing detergents.
Extrakte des OlivenbaumesExtracts of the olive tree
Die Herstellung der erfindungsgemäß einzusetzenden Extrakte erfolgt durch übliche Methoden der Extraktion. Bezüglich der geeigneten herkömmlichen Extraktionsverfahren wie der Mazeration, der Remazeration, der Digestion, der Bewegungsmazeration, der Wirbelextraktion, Ultraschallextraktion, der Gegenstromextraktion, der Perkolation, der Reperkolation, der Evakolation (Extraktion unter vermindertem Druck), der Diakolation und Festflüssig-Extraktion unter kontinuierlichem Rückfluß, die in einem Soxhiet-Extraktor durchgeführt wird, die dem Fachmann geläufig und im Prinzip alle anwendbar sind, sei beispielhaft auf Hagers Handbuch der Pharmazeutischen Praxis, (5. Auflage, Bd. 2, S. 1026-1030, Springer Verlag, Berlin-Heidelberg-New-York 1991) verwiesen. Als Ausgangsmaterial können frische oder getrocknete Teile des Olivenbaumes eingesetzt werden, üblicherweise wird jedoch von Blättern ausgegangen, die vor der Extraktion mechanisch zerkleinert werden. Hierbei eignen sich alle dem Fachmann bekannten Zerkleinerungsmethoden, als Beispiel sei die Zerstoßung mit einem Mörser genannt.The extracts to be used according to the invention are prepared by customary extraction methods. Regarding the suitable conventional extraction methods such as maceration, remaceration, digestion, movement maceration, vortex extraction, ultrasound extraction, countercurrent extraction, percolation, repercolation, evacolation (extraction under reduced pressure), diacolation and solid-liquid extraction under continuous reflux , which is carried out in a Soxhiet extractor, which is familiar to a person skilled in the art and in principle all can be used, is exemplary of Hager's Handbook of Pharmaceutical Practice, (5th edition, vol. 2, pp. 1026-1030, Springer Verlag, Berlin- Heidelberg-New-York 1991). Fresh or dried parts of the olive tree can be used as the starting material, but usually leaves are used which are mechanically shredded before extraction. All grinding methods known to the person skilled in the art are suitable here, for example crushing with a mortar.
Als Lösungsmittel für die Durchführung der Extraktionen können vorzugsweise Wasser, organische Lösungsmittel oder Gemische aus organischen Lösungsmitteln und Wasser, insbesondere niedermolekulare Alkohole, Kohlenwasserstoffe, Ketone, Ester oder halogenhaltige Kohlenwasserstoffe mit mehr oder weniger hohen Wassergehalten (destilliert oder nicht destilliert) vorzugsweise wässrig, alkoholische Lösungen einer Temperatur von größer oder gleich 20 °C verwendet werden. Besonders bevorzugt ist die Extraktion mit Wasser, Methanol, Ethanol, Hexan, Cyclohexan, Pentan, Aceton, Propy- lenglycolen, Polyethylenglycolen, Ethylacetat, Dichlormethan, Trichlormethan sowie Mischungen hier- aus. Die Extraktion erfolgt in der Regel bei 20 bis 100 °C, bevorzugt bei 20 bis 85°C, insbesondere entweder bei Siedetemperatur des verwendeten Lösungsmittels oder bei Raumtemperatur. In einer möglichen Ausführungsform erfolgt die Extraktion unter Inertgasatmosphäre zur Vermeidung der Oxi- dation der Inhaltsstoffe des Extraktes. Die Extraktionszeiten werden vom Fachmann in Abhängigkeit vom Ausgangsmaterial, dem Extraktionsverfahren, der Extraktionstemperatur, vom Verhältnis Lösungsmittel zu Rohstoff u.a. eingestellt. Nach der Extraktion können die erhaltenen Rohextrakte gegebenenfalls weiteren üblichen Schritten, wie beispielsweise Aufreinigung, Konzentration und/oder Entfärbung unterzogen werden. Falls wünschenswert, können die so hergestellten Extrakte beispielsweise einer selektiven Abtrennung einzelner unerwünschter Inhaltsstoffe, unterzogen werden. Die Extraktion kann bis zu jedem gewünschten Extraktionsgrad erfolgen, wird aber gewöhnlich bis zur Erschöpfung durchgeführt. Die vorliegende Erfindung umfasst die Erkenntnis, dass die Extraktionsbedingungen sowie die Ausbeuten der Endextrakte je nach gewünschtem Einsatzgebiet gewählt werden können. Falls gewünscht, können die Extrakte anschließend beispielsweise einer Sprüh- oder Gefriertrocknung unterworfen werden.Water, organic solvents or mixtures of organic solvents and water, in particular low molecular weight alcohols, hydrocarbons, ketones, esters or halogen-containing hydrocarbons with more or less high water contents (distilled or not distilled), preferably aqueous, alcoholic solutions, can preferably be used as solvents for carrying out the extractions a temperature of greater than or equal to 20 ° C can be used. Extraction with water, methanol, ethanol, hexane, cyclohexane, pentane, acetone, propylene glycols, polyethylene glycols, ethyl acetate, dichloromethane, trichloromethane and mixtures thereof is particularly preferred. out. The extraction is usually carried out at 20 to 100 ° C, preferably at 20 to 85 ° C, in particular either at the boiling point of the solvent used or at room temperature. In one possible embodiment, the extraction takes place under an inert gas atmosphere to avoid oxidation of the ingredients of the extract. The extraction times are set by the person skilled in the art depending on the starting material, the extraction process, the extraction temperature, the ratio of solvent to raw material, etc. After the extraction, the crude extracts obtained can optionally be subjected to further customary steps, such as purification, concentration and / or decolorization. If desired, the extracts produced in this way can, for example, be subjected to a selective separation of individual undesirable ingredients. The extraction can be carried out to any desired degree of extraction, but is usually carried out until exhaustion. The present invention includes the knowledge that the extraction conditions and the yields of the final extracts can be selected depending on the desired field of use. If desired, the extracts can then be subjected to spray drying or freeze drying, for example.
Die Einsatzmenge der Extrakte in den genannten Zubereitungen richtet sich nach der Art der Anwendungen der Extrakte und nach der Konzentration der einzelnen Inhaltstoffe. Die Gesamtmenge des Olivenbaumblätterextraktes, der in den erfindungsgemäßen Zubereitungen enthalten ist, beträgt in der Regel 0,01 bis 15 Gew.-%, vorzugsweise 0,05 bis 5 Gew.-%, insbesondere 0,1 bis 3 Gew.-% bezogen auf die Endzubereitung, mit der Maßgabe, dass sich die Mengenangaben mit Wasser und gegebenenfalls weiteren Hilfs- und Zusatzstoffen zu 100 Gew.-% addieren.The amount of the extracts used in the preparations mentioned depends on the type of application of the extracts and on the concentration of the individual ingredients. The total amount of the olive tree leaf extract which is contained in the preparations according to the invention is generally 0.01 to 15% by weight, preferably 0.05 to 5% by weight, in particular 0.1 to 3% by weight, based on the final preparation, with the proviso that the quantities with water and possibly other auxiliary substances and additives add up to 100% by weight.
Vorzugsweise werden Olivenbaumblätterextrakte eingesetzt die bezüglich Ihres Hauptinhaltsstoffes Oleuropein standardisiert sind. Sie enthalten 1 bis 40 Gew. % vorzugsweise 5 bis 30 Gew. %, besonders bevorzugt 10 bis 25 Gew. % und speziell 18 bis 22 Gew. % Oleuropein bezogen auf den Trockenextrakt.Olive tree leaf extracts are preferably used, which are standardized with regard to their main ingredient oleuropein. They contain 1 to 40% by weight, preferably 5 to 30% by weight, particularly preferably 10 to 25% by weight and especially 18 to 22% by weight oleuropein, based on the dry extract.
Extrakte aus dem Abwasser der Olivenbaumherstellung werden durch Trocknung des Wasser vorzugsweise über Sprühtrocknung nach Zusatz von Hilfsstoffen wie Mannitol oder Natriumcaseinat hergestellt. Sie werden auf einen Gehalt an Polyphenolen, vorzugsweise Hydroxytyrosol und Tyrosol eingestellt, dieser beträgt mindestens 0,5 Gew. % vorzugsweise mindestens 1 Gew. % und besonders bevorzugt mindestens 2 Gew. % Polyphenol bezogen auf den Trockenextrakt.Extracts from the wastewater of olive tree production are produced by drying the water, preferably by spray drying, after addition of auxiliaries such as mannitol or sodium caseinate. They are adjusted to a content of polyphenols, preferably hydroxytyrosol and tyrosol, which is at least 0.5% by weight, preferably at least 1% by weight and particularly preferably at least 2% by weight, based on the dry extract.
Aktivsubstanz im Sinne der Erfindung bezieht sich auf den Anteil an Substanzen sowie Hilfs- und Zusatzstoffen, die in den Zubereitungen enthaltend sind, mit Ausnahme des zusätzlich hinzugefügten Wassers. Wasch- , Spül- oder ReinigungsmittelActive substance in the sense of the invention relates to the proportion of substances and auxiliaries and additives which are contained in the preparations, with the exception of the additionally added water. Detergent, dishwashing detergent or cleaning agent
Ein weiterer Gegenstand der Erfindung sind Wasch-, Spül- oder Reinigungsmittel-Zubereitungen, enthaltend Extrakte aus den Blättern des Olivenbaumes und/oder aus dem Abwasser der Olivenölherstellung und mindestens 10 Gew. %, bevorzugt mindestens 15 Gew. % und besonders bevorzugt mindestens 20 Gew.% an Aktivsubstanz eines anionischen und/oder kationischen und/oder amphoteren und/oder nichtionischen Tensides - bezogen auf die Zubereitung.Another object of the invention are washing, rinsing or cleaning agent preparations containing extracts from the leaves of the olive tree and / or from the wastewater of olive oil production and at least 10% by weight, preferably at least 15% by weight and particularly preferably at least 20% by weight .% of active substance of an anionic and / or cationic and / or amphoteric and / or nonionic surfactant - based on the preparation.
Gegenstand der vorliegenden Erfindung betrifft auch die Verwendung der Olivenbaumextrakte zur Herstellung von Wasch-, Spül- und Reinigungsmitteln.The present invention also relates to the use of the olive tree extracts for the production of washing, rinsing and cleaning agents.
Übliche Wasch-, Spül- und Reinigungsmittel enthalten - bezogen auf die Zubereitung - beispielsweise 0,01 bis 15 Gew.% Extrakte aus den Blättern des Olivenbaumes und/oder aus dem Abwasser der Olivenölherstellung und mindestens 10 Gew.% Aktivsubstanz eines anionischen und/oder kationischen und/oder amphoteren und/oder nichtionischen Tensides, vorzugsweise enthalten sie 0,05 bis 5 Gew.% Extrakte aus den Blättern des Olivenbaumes und/oder aus dem Abwasser der Olivenölherstellung und mindestens 15 Gew. % Aktivsubstanz eines anionischen und/oder kationischen und/oder amphoteren und/oder nichtionischen Tensides, und besonders bevorzugt 0,1 bis 3 Gew.% Extrakte aus den Blättern des Olivenbaumes und/oder aus dem Abwasser der Olivenölherstellung und mindestens 20 Gew. % Aktivsubstanz eines anionischen und/oder kationischen und/oder amphoteren und/oder nichtionischen Tensides.Common detergents, dishwashing detergents and cleaning agents contain - based on the preparation - for example 0.01 to 15% by weight of extracts from the leaves of the olive tree and / or from the wastewater of olive oil production and at least 10% by weight of active substance of an anionic and / or cationic and / or amphoteric and / or nonionic surfactants, preferably they contain 0.05 to 5% by weight of extracts from the leaves of the olive tree and / or from the wastewater from olive oil production and at least 15% by weight of active substance of an anionic and / or cationic and / or amphoteric and / or nonionic surfactants, and particularly preferably 0.1 to 3% by weight of extracts from the leaves of the olive tree and / or from the waste water from olive oil production and at least 20% by weight of active substance of an anionic and / or cationic and / or amphoteric and / or nonionic surfactants.
Es ist dabei möglich die Extrakte auch mit hohen Mengen an Tensiden einzusetzen. Die Reinigungskapazität und die Schaumqualität der Zubereitungen wird durch den Zusatz der Extrakte des Olivenbaumes nicht gemindert.It is also possible to use the extracts with high amounts of surfactants. The cleaning capacity and the foam quality of the preparations are not reduced by the addition of extracts from the olive tree.
Je nach Anwendungsgebiet werden den Zubereitungen stark schäumende oder milde, pflegende Ten- side zugesetzt. Bevorzugt werden die Extrakte auf Grund ihrer guten Hautverträglichkeit in Handgeschirrspülmitteln und Körperwaschmitteln eingesetzt.Depending on the area of application, strongly foaming or mild, nourishing surfactants are added to the preparations. Because of their good skin tolerance, the extracts are preferably used in hand dishwashing detergents and body detergents.
HandgeschirrspülmittelHand dishwashing detergents
Die erfindungsgemäßen Handgeschirrspülmittel enthalten als Tenside vorzugsweise Alk(en)yloligoglycoside.The hand dishwashing detergents according to the invention preferably contain alk (en) yl oligoglycosides as surfactants.
Alkyl- und AlkenyloligoαlvkosideAlkyl and Alkenyloligoαlvkoside
Die in denHandgeschirrspülmitteln vorzugsweise enthaltenen Alkyl- und Alkenyloligoglykoside folgen der Formel (I), R 0-[G]P (I)The alkyl and alkenyl oligoglycosides preferably contained in the hand dishwashing detergents follow the formula (I) R 0- [G] P (I)
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 einschlägigen Verfahren der präparativen organischen Chemie erhalten werden.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 procedures in preparative organic chemistry.
Die Alkyl- und/oder Alkenyloligoglykoslde können sich von Aldosen bzw. Ketosen mit 5 oder 6 Kohlenstoffatomen, vorzugsweise der Glucose ableiten. Die bevorzugten Alkyl und/oder Alkenyloligoglykoslde sind somit Alkyl- und/oder Alkenyloligoglucoside. Die Indexzahl p in der allgemeinen Formel (I) gibt den Ollgomerisierungsgrad (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 Alkenyloligoglykoslde mit einem mittleren Ollgomerisierungsgrad p von 1,1 bis 3,0 eingesetzt. Aus anwendungstechnischer Sicht sind solche Alkyl- und/oder Alkenyloligoglykoslde bevorzugt, deren Ollgomerisierungsgrad 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 Alkyloli- goglucoside der Kettenlänge Cβ-Cio (DP = 1 bis 3), die als Vorlauf bei der destillativen Auftrennung von technischem Cs-Cis-Kokosfettalkohol anfallen und mit einem Anteil von weniger als 6 Gew.-% C12- Alkohol verunreinigt sein können sowie Alkyloligoglucoside auf Basis technischer Cg/n-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, Elai- dylalkohol, Petroselinylalkohol, Arachylalkohol, Gadoleylalkohol, Behenylalkohol, Erucylalkohol, Brassi- dylalkohol sowie deren technische Gemische, die wie oben beschrieben erhalten werden können. Bevorzugt sind Alkyloligoglucoside auf Basis von gehärtetem Ci2/i4-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 olomerization (DP), ie the distribution of mono- and oligoglycosides, and stands for a number between 1 and 10. While p in a given compound must always be an integer, 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 is 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. Alkyl oligoglucosides of chain length Cβ-Cio (DP = 1 to 3) are preferred, which are obtained as a preliminary step in the separation of technical Cs-Cis-coconut fatty alcohol by distillation and are contaminated with a proportion of less than 6% by weight of C12 alcohol can as well as alkyl oligoglucosides based on technical Cg / n-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, alaidyl alcohol, petroselinyl alcohol, arachyl alcohol, gadoleyl alcohol, behenyl alcohol, erucyl alcohol, brassidyl alcohol and their technical mixtures, which can be obtained as well as their technical mixtures. Alkyl oligoglucosides based on hydrogenated Ci2 / i4 coconut alcohol with a DP of 1 to 3 are preferred.
Weitere nichtionische TensideOther non-ionic surfactants
Die erfindungsgemäßen Handgeschirrspülmittel können abgesehen von den Alkyl- und Alkenyloligogly- kosiden weitere nichtionische Tenside enthalten. Typische Beispiele für nichtionische Tenside sind alkoxylierten Carbonsäureester, Hydroxymischether, Fettalkoholpolyglycolether, Alkylphenolpolyglycol- ether, Fettsäureamidpolyglycolether, Fettaminpolyglycolether, alkoxylierte Triglyceride, Fettsäure-N- alkyl-glucamide, 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.Apart from the alkyl and alkenyl oligoglycosides, the hand dishwashing detergents according to the invention can contain further nonionic surfactants. Typical examples of nonionic surfactants are alkoxylated carboxylic acid esters, hydroxy mixed ethers, fatty alcohol polyglycol ethers, alkylphenol polyglycol ether, fatty acid amide polyglycol ether, fatty amine polyglycol ether, alkoxylated triglycerides, fatty acid N-alkyl-glucamides, protein hydrolysates (especially vegetable products based on wheat), 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.
Bevorzugt sind weitere nichtionische Tenside ausgewählt aus der Gruppe, die gebildet wird von alkoxy- lierten Carbonsäureestern, Hydroxymischethem, Fettalkoholpolyglycolether.n endgruppen- verschlossenen Fettalkoholpolyglycolethern, Aminoxiden und Fettsäure-N-alkyl-glucamiden.Other nonionic surfactants are preferably selected from the group formed by alkoxylated carboxylic acid esters, hydroxy mixed ethers, fatty alcohol polyglycol ethers, end group-capped fatty alcohol polyglycol ethers, amine oxides and fatty acid N-alkyl glucamides.
Aniontensideanionic surfactants
Die erfindungsgemäßen Mittel können anionische Tenside enthalten. Typische Beispiele für anionische Tenside sind Seifen, Alkylbenzolsulfonate, Alkansulfonate, Olefinsulfonate, Alkylethersulfonate, Glyce- rinethersulfonate, α-Methylestersulfonate, Sulfofettsäuren, Alkyl- und/oder Alkenylsulfate, Alkylether- sulfate, Glycerinethersulfate, Monoglycerid(ether)sulfate, Hydroxymischethersulfate, Fettsäureamid- (ether)sulfate, Mono- und Dialkylsulfosuccinate, Mono- und Dialkylsulfosuccinamate, Sulfotriglyceride, Amidseifen, Ethercarbonsäuren und deren Salze, Fettsäureisethionate, Fettsäuresarcosinate, Fettsäu- retauride, N-Acylaminosäuren wie beispielsweise Acyllactylate, Acyltartrate, Acylglutamate und Acy- laspartate, 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.The agents according to the invention can contain anionic surfactants. Typical examples of anionic surfactants are soaps, alkyl benzene sulfonates, alkane sulfonates, olefin sulfonates, alkyl ether sulfonates, glycerol ether sulfonates, α-methyl ester sulfonates, sulfo fatty acids, alkyl and / or alkenyl sulfates, alkyl ether sulfates, glycerol ether sulfates, fatty acid monoglyid sulfate (ether sulfate amide), monoglyid sulfate (ether) ether) sulfates, mono- and dialkylsulfosuccinates, mono- and dialkylsulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid isethionates, fatty acid sarcosinates, fatty acid retaurides, N-acylamino acids such as acyl lactylates, acyl glutolate glucate, acyl glolate glycate, acyl glolate glycate, acyl glolate glucosate, especially 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.
Vorzugsweise werden Alkyl- und/oder Alkenylsulfate, Alkylethersulfate, Alkansulfonate, Monoglyce- rid(ether)sulfate, Alkylbenzolsulfonate, Sulfosuccinate und/oder Fettsäurepolyglykolestersulfate, insbesondere Fettalkoholsulfate, Fettalkoholethersulfate eingesetzt.Alkyl and / or alkenyl sulfates, alkyl ether sulfates, alkane sulfonates, monoglyceride (ether) sulfates, alkyl benzene sulfonates, sulfosuccinates and / or fatty acid polyglycol ester sulfates, in particular fatty alcohol sulfates, fatty alcohol ether sulfates, are preferably used.
Amphotere bzw. zwitterionische TensideAmphoteric or zwitterionic surfactants
In einer weiteren Ausführungsform enthalten die erfindungsgemäßen Handgeschirrspülmittel amphotere bzw. zwitterionische Tenside. Typische Beispiele für amphotere bzw. zwitterionische Tenside sind Alkylbetaine, Alkylamidobetaine, Aminopropionate, Imidazoliniumbetaine und Sulfobetaine.In a further embodiment, the hand dishwashing detergents according to the invention contain amphoteric or zwitterionic surfactants. Typical examples of amphoteric or zwitterionic surfactants are alkyl betaines, alkyl amido betaines, aminopropionates, imidazolinium betaines and sulfobetaines.
Betaine stellen bekannte Tenside dar, die überwiegend durch Carboxyalkylierung, vorzugsweise Car- boxymethylierung von aminischen Verbindungen hergestellt werden. Vorzugsweise werden die Ausgangsstoffe mit Halogencarbonsäuren oder deren Salzen, insbesondere mit Natriumchloracetat kon- densiert, wobei pro Mol Betain ein Mol Salz gebildet wird. Ferner ist auch die Anlagerung von ungesättigten Carbonsäuren, wie beispielsweise Acrylsäure möglich.Betaines are known surfactants which are predominantly produced by carboxyalkylation, preferably carboxymethylation, of aminic compounds. The starting materials are preferably contacted with halocarboxylic acids or their salts, in particular with sodium chloroacetate. dense, forming one mole of salt per mole of betaine. The addition of unsaturated carboxylic acids, such as acrylic acid, is also possible.
Weitere Hilfs- und ZusatzstoffeOther auxiliaries and additives
Fakultativ können den wäßrigen Handgeschirrspülmitteln übliche Hilfsstoffe wie Builder, z.B. Glutar- säure, Bernsteinsäure, Adipinsäure, Weinsäure, Gluconsäure, Trinatriumcitrat, Lösungsmittel, z.B. Aceton oder Ethanol, Hydrotrope, z.B. Cumolsulfonat, Butylglucosid, Butylenglykol, Viskositätsregler wie z.B. Fettsäurealkanolamide, pH-Regulatoren, z.B. Zitronensäure, Natron- und Kalilauge, Perglanzmittel wie z.B. Stearinsäurederivate. Außerdem können Farbstoffe und auch Duftstoffe enthalten sein.Optional auxiliary agents such as builders, e.g. Glutaric acid, succinic acid, adipic acid, tartaric acid, gluconic acid, trisodium citrate, solvents, e.g. Acetone or ethanol, hydrotrope e.g. Cumene sulfonate, butyl glucoside, butylene glycol, viscosity regulators such as Fatty acid alkanolamides, pH regulators, e.g. Citric acid, caustic soda and potassium hydroxide, pearlescent agents such as Stearic acid derivatives. It can also contain dyes and fragrances.
Die Handgeschirrspülmittel können selbstverständlich weitere antimikrobiell wirksame Wirkstoffe enthalten. Vorzugsweise werden dazu quaternierte Ammoniumverbindungen, quaternierten Fettsäu- retriethanolaminestersalzen (Esterquats) und/oder aromatischen Alkoholen eingesetzt.The hand dishwashing detergents can of course contain other antimicrobial active ingredients. Quaternized ammonium compounds, quaternized fatty acid triethanolamine ester salts (esterquats) and / or aromatic alcohols are preferably used for this purpose.
Duftstoffefragrances
Als Parfümöle bzw. Duftstoffe können einzelne Riechstoffverbindungen, z.B. die synthetischen Produkte vom Typ der Ester, Ether, Aldehyde, Ketone, Alkohole und Kohlenwasserstoffe verwendet werden. Riechstoffverbindungen vom Typ der Ester sind z.B. Benzylacetat, Phenoxyethylisobutyrat, p-tert.- Butylcyclohexylacetat, Linalylacetat, Dimethylbenzylcarbinylacetat, Phenylethylacetat, Linalylbenzoat, Benzylformiat, Ethylmethylphenylglycinat, Allylcyclohexylpropionat, Styrallylpropionat und Benzylsali- cylat. Zu den Ethern zählen beispielsweise Benzylethylether, zu den Aldehyden z.B. die linearen Alkanale mit 8-18 C-Atomen, Citral, Citronellal, Citronellyloxyacetaldehyd, Cyclamenaldehyd, Hydroxycitro- nellal, Lilial und Bourgeonal, zu den Ketonen z.B. die Jonone, α-lsomethylionon und Methylcedrylke- ton, zu den Alkoholen Anethol, Citronellol, Eugenol, Geraniol, Linalool, Phenylethylalkohol und Terpi- neol, zu den Kohlenwasserstoffen gehören hauptsächlich die Terpene wie Limonen und Pinen. Bevorzugt werden jedoch Mischungen verschiedener Riechstoffe verwendet, die gemeinsam eine ansprechende Duftnote erzeugen. Solche Parfümöle können auch natürliche Riechstoffgemische enthalten, wie sie aus pflanzlichen Quellen zugänglich sind, z.B. Pine-, Citrus-, Jasmin-, Patchouly-, Rosen- oder Ylang-Ylang-Öl. Ebenfalls geeignet sind Muskateller, Salbeiöl, Kamillenöl, Nelkenöl, Melissenöl, Minzöl, Zimtblätteröl, Lindenblütenöl, Wacholderbeeröl, Vetiveröl, Olibanumöl, Galbanumöl und Labdanumöl sowie Orangenblütenöl, Neroliol, Orangenschalenöl und Sandelholzöl. KörperwaschmittelIndividual fragrance compounds, for example the synthetic products of the ester, ether, aldehyde, ketone, alcohol and hydrocarbon type, can be used as perfume oils or fragrances. Fragrance compounds of the ester type are, for example, benzyl acetate, phenoxyethyl isobutyrate, p-tert.-butylcyclohexyl acetate, linalyl acetate, dimethylbenzylcarbinyl acetate, phenylethyl acetate, linalyl benzoate, benzyl formate, ethyl methylphenylglycinate, allylcyclohexyl benzylatepylpropionate, stally. The ethers include, for example, benzyl ethyl ether, the aldehydes, for example, the linear alkanals with 8-18 C atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamenaldehyde, hydroxycitronellal, lilial and bourgeonal, and the ketones include, for example, the jonones, α-isomethylionone and methylcedrylke - clay, the alcohols anethole, citronellol, eugenol, geraniol, linalool, phenylethyl alcohol and terpinol, the hydrocarbons mainly include the terpenes such as limonene and pinene. However, preference is given to using mixtures of different fragrances which together produce an appealing fragrance. Perfume oils of this type can also contain natural fragrance mixtures such as are obtainable from plant sources, for example pine, citrus, jasmine, patchouly, rose or ylang-ylang oil. Also suitable are muscatel, sage oil, chamomile oil, clove oil, lemon balm oil, mint oil, cinnamon leaf oil, linden blossom oil, juniper berry oil, vetiver oil, olibanum oil, galbanum oil and labdanum oil as well as orange blossom oil, neroliol, orange peel oil and sandalwood oil. body wash
Die erfindungsgemäßen Körperwaschmittel können als Haarshampoos, Schaumbäder, Duschbäder, Waschlotionen oder Seifenstücke vorliegen. Diese Mittel können ferner als weitere Hilfs- und Zusatzstoffe milde Tenside, Ölkörper, Emulatoren, Perlglanzwachse, Konsistenzgeber, Verdickungsmittel, Überfettungsmittel, Stabilisatoren, Polymere, Siliconverbindungen, Fette, Wachse, Lecithine, Phospho- lipide, biogene Wirkstoffe, Antischuppenmittel, Filmbildner, Hydrotrope, Solubilisatoren, Konservierungsmittel, Parfümöle, Farbstoffe und dergleichen enthalten.The body detergents according to the invention can be present as hair shampoos, foam baths, shower baths, washing lotions or bars of soap. These agents can also be used as further auxiliaries and additives, mild surfactants, oil bodies, emulators, pearlescent waxes, consistency agents, thickeners, superfatting agents, stabilizers, polymers, silicone compounds, fats, waxes, lecithins, phospholipids, biogenic active ingredients, antidandruff agents, film formers, hydrotropes, Contain solubilizers, preservatives, perfume oils, dyes and the like.
Tensidesurfactants
Als oberflächenaktive Stoffe können anionische, nichtionische, kationische und/oder amphotere bzw. zwitterionische Tenside enthalten sein, deren Anteil an den Mitteln üblicherweise bei etwa 1 bis 70, vorzugsweise 5 bis 50 und insbesondere 10 bis 30 Gew.-% beträgt. Typische Beispiele für anionische Tenside sind Seifen, Alkylbenzolsulfonate, Alkansulfonate, Olefinsulfonate, Alkylethersulfonate, Glyce- rinethersulfonate, α-Methylestersulfonate, Sulfofettsäuren, Alkylsulfate, Fettalkoholethersulfate, Glyce- rinethersulfate, Fettsäureethersulfate, Hydroxymischethersulfate, Monoglycerid(ether)sulfate, Fettsäu- reamid(ether)sulfate, Mono- und Dialkylsulfosuccinate, Mono- und Dialkylsulfosuccinamate, Sulfotri- glyceride, Amidseifen, Ethercarbonsäuren und deren Salze, Fettsäureisethionate, Fettsäuresarcosi- nate, Fettsäuretauride, N-Acylaminosäuren, wie beispielsweise Acyllactylate, Acyltartrate, Acylgluta- mate und Acylaspartate, 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 Fettalko- holpolyglycolether, Alkylphenolpolyglycolether, Fettsäurepolyglycolester, Fettsäureamidpolyglycolether, Fettaminpolyglycolether, alkoxylierte Triglyceride, Mischether bzw. Mischformale, gegebenenfalls partiell oxidierte Alk(en)yloligoglykoside bzw. Glucoronsäurederivate, Fettsäure-N-alkylglucamide, Protein- hydrolysate (insbesondere pflanzliche Produkte auf Weizenbasis), Polyolfettsäureester, 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, wie beispielsweise das Dimethyldistearylammoniumchlorid, und Esterquats, insbesondere quaternierte Fettsäuretrialkanolaminestersalze. Typische Beispiele für amphotere bzw. zwitterionische Tenside sind Alkylbetaine, Alkylamidobetaine, Aminopropionate, Aminoglycinate, Imidazoliniumbetaine und Sulfo- betaine. Bei den genannten Tensiden handelt es sich ausschließlich um bekannte Verbindungen. Typische Beispiele für besonders geeignete milde, d.h. besonders hautverträgliche Tenside sind Fettalko- holpolyglycolethersulfate, Monoglyceridsulfate, Mono- und/oder Dialkylsulfosuccinate, Fettsäureisethio- nate, Fettsäuresarcosinate, Fettsäuretauride, Fettsäureglutamate, α-Olefinsulfonate, Ethercarbonsäu- ren, Alkyloligoglucoside, Fettsäureglucamide, Alkylamidobetaine, Amphoacetale und/oder Proteinfettsäurekondensate, letztere vorzugsweise auf Basis von Weizenproteinen.Anionic, nonionic, cationic and / or amphoteric or zwitterionic surfactants may be present as surface-active substances, the proportion of which in the compositions is usually about 1 to 70, preferably 5 to 50 and in particular 10 to 30% by weight. Typical examples of anionic surfactants are soaps, alkyl benzene sulfonates, alkane sulfonates, olefin sulfonates, alkyl ether sulfonates, glycerol ether sulfonates, α-methyl ester sulfonates, sulfo fatty acids, alkyl sulfates, fatty alcohol ether sulfates, glycerol ether sulfates, fatty acid ether sulfates, ether ether sulfates (mono) ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, mono ether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, hydroxymether ether sulfates, mono ether sulfates, sulfates, mono- and dialkylsulfosuccinates, mono- and dialkylsulfosuccinamates, sulfotriglycerides, amide soaps, ether carboxylic acids and their salts, fatty acid isethionates, fatty acid sarcosines, fatty acid taurides, N-acylamino acids, such as acyl lactylates, acyl sulfate fucylate, acyl acylate fate (especially 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, alkylphenol 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 (especially glucoronic acid derivatives) Wheat-based products), 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, such as, for example, dimethyldistearylammonium chloride, and esterquats, in particular quaternized fatty acid trialkanolamine ester salts. Typical examples of amphoteric or zwitterionic surfactants are alkyl betaines, alkyl amido betaines, aminopropionates, aminoglycinates, imidazolinium betaines and sulfobetaines. The surfactants mentioned are exclusively known compounds. Typical examples of particularly suitable mild, ie particularly skin-compatible surfactants are fatty alcohol polyglycol ether sulfates, monoglyceride sulfates, mono- and / or dialkyl sulfosuccinates, fatty acid isethio nates, fatty acid sarcosinates, fatty acid taurides, fatty acid glutamates, α-olefin sulfonates, ether carboxylic acids, alkyl oligoglucosides, fatty acid glucamides, alkyl amido betaines, amphoacetals and / or protein fatty acid condensates, the latter preferably based on wheat proteins.
Ölkörperoil body
Als Ölkörper kommen 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-Ci3-Carbonsäuren mit linearen oder verzweigten C6-C22-Fettalkoholen, wie z.B. Myristylmyristat, Myristylpalmitat, Myristylstearat, Myristyli- sostearat, Myristyloleat, Myristylbehenat, Myristylerucat, Cetylmyristat, Cetylpalmitat, Cetylstearat, Ce- tylisostearat, Cetyloleat, Cetylbehenat, Cetylerucat, Stearylmyristat, Stearylpalmitat, Stearylstearat, Stearylisostearat, Stearyloleat, Stearylbehenat, Stearylerucat, Isostearylmyristat, Isostearylpalmitat, Isostearylstearat, Isostearylisostearat, Isostearyloleat, Isostearylbehenat, Isostearyloleat, Oleylmyristat, Oleylpalmitat, Oleylstearat, Oleylisostearat, Oleyloleat, Oleylbehenat, Oleylerucat, Behenylmyristat, Behenylpalmitat, Behenylstearat, Behenylisostearat, Behenyloleat, Behenylbehenat, Behenylerucat, Erucylmyristat, Erucylpalmitat, Erucylstearat, Erucylisostearat, Erucyloleat, Erucylbehenat und Erucyle- rucat. Daneben eignen sich Ester von linearen C6-C22-Fettsäuren mit verzweigten Alkoholen, insbesondere 2-Ethylhexanol, Ester von Ci8-C38-Alkylhydroxycarbonsäuren mit linearen oder verzweigten C6-C22-Fettalkoholen, insbesondere Dioctyl Malate, Ester von linearen und/oder verzweigten Fettsäuren mit mehrwertigen Alkoholen (wie z.B. Propylenglycol, Dimerdiol oder Trimertriol) und/oder Guerbetalko- holen, Triglyceride auf Basis C6-Cιo-Fettsäuren, flüssige Mono-/Di-/Triglyceridmischungen auf Basis von Cθ-Cis-Fettsäuren, Ester von C6-C22-Fettalkoholen und/oder Guerbetalkoholen mit aromatischen Carbonsäuren, insbesondere Benzoesäure, Ester von C2-Ci2-Dicarbonsäuren mit linearen oder verzweigten Alkoholen mit 1 bis 22 Kohlenstoffatomen oder Polyolen mit 2 bis 10 Kohlenstoffatomen und 2 bis 6 Hydroxylgruppen, pflanzliche Öle, verzweigte primäre Alkohole, substituierte Cyclohexane, lineare und verzweigte C6-C22-Fettalkoholcarbonate, wie z.B. Dicaprylyl Carbonate (Cetiol® CC), Guer- betcarbonate 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 Al- kylgruppe, 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 in Betracht. EmulatorenGuerbet alcohols based on fatty alcohols with 6 to 18, preferably 8 to 10 carbon atoms, esters of linear C6-C22 fatty acids with linear or branched C6-C22 fatty alcohols or esters of branched C6-Ci3 carboxylic acids with linear or branched C6-C22-fatty alcohols, such as myristyl myristate, myristyl palmitate sostearat, myristyl stearate, Myristyli-, myristyl, Myristylbehenat, Myristylerucat, cetyl myristate, cetyl palmitate, cetyl stearate, Ce tylisostearat, cetyl oleate, cetyl behenate, Cetylerucat, Stearylmyristat, stearyl palmitate, stearyl stearate, Stearylisostearat, stearyl oleate , stearyl behenate, Stearylerucat, isostearyl, isostearyl palmitate, Isostearylstearat, isostearyl isostearate, Isostearyloleat, isostearyl behenate, Isostearyloleat, oleyl myristate, oleyl palmitate, oleyl stearate, oleyl isostearate, oleyl oleate, Oleylbehenat, oleyl erucate, behenyl myristate, behenyl palmitate, behenyl, Behenylisostearat, behenyl oleate, Behenylbehen at, behenyl erucate, erucyl myristate, erucyl palmitate, erucyl stearate, erucyl isostearate, erucyl oleate, erucyl behenate and erucyl rucate. In addition, esters of linear C6-C22 fatty acids with branched alcohols, in particular 2-ethylhexanol, esters of Ci8-C38 alkylhydroxycarboxylic acids with linear or branched C6-C22 fatty alcohols, in particular dioctyl malates, esters of linear and / or branched fatty acids are also suitable polyhydric alcohols (such as propylene glycol, dimer diol or trimer triol) and / or Guerbet alcohols, triglycerides based on C6-Cιo fatty acids, liquid mono- / di- / triglyceride mixtures based on Cθ-Cis fatty acids, esters of C6-C22- Fatty alcohols and / or Guerbet alcohols with aromatic carboxylic acids, especially benzoic acid, esters of C2-Ci2-dicarboxylic acids with linear or branched alcohols with 1 to 22 carbon atoms or polyols with 2 to 10 carbon atoms and 2 to 6 hydroxyl groups, vegetable oils, branched primary alcohols Cyclohexanes, linear and branched C6-C22 fatty alcohol carbonates, such as, for example, dicaprylyl carbonates (Cetiol® CC), Guerbetcarbona te based on fatty alcohols with 6 to 18, preferably 8 to 10 C atoms, esters of benzoic acid with linear and / or branched C6-C22 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. emulators
Als Emulgatoren kommen beispielsweise nichtionogene Tenside aus mindestens einer der folgenden Gruppen in Frage:Examples of suitable emulsifiers are nonionic surfactants from at least one of the following groups:
> Anlagerungsprodukte von 2 bis 30 Mol Ethylenoxid und/ oder 0 bis 5 Mol Propylenoxid an lineare> Addition products of 2 to 30 mol ethylene oxide and / or 0 to 5 mol propylene oxide on linear
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;Fatty alcohols with 8 to 22 carbon atoms, fatty acids with 12 to 22 carbon atoms, alkylphenols with 8 to 15 carbon atoms in the alkyl group and alkylamines with 8 to 22 carbon atoms in the alkyl radical;
> Alkyl- und/oder Alkenyloligoglykoslde mit 8 bis 22 Kohlenstoffatomen im Alk(en)ylrest und deren ethoxylierte Analoga;> Alkyl and / or alkenyl oligoglycosides with 8 to 22 carbon atoms in the alk (en) yl radical and their ethoxylated analogs;
> Anlagerungsprodukte von 1 bis 15 Mol Ethylenoxid an Ricinusöl und/oder gehärtetes Ricinusöl;> Adducts of 1 to 15 moles of ethylene oxide with castor oil and / or hardened castor oil;
> 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), Polyethylengly- col (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 polyglycerol (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 (e.g. cellulose) / or 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 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 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. Polyethy leng lycol-30 Dipolyhydroxystearate; Polymeremulgatoren, z.B. Pemulen-Typen (TR-1 ,TR-2) von Goodrich;> Block copolymers e.g. Polyethylene glycol-30 dipolyhydroxystearate; Polymer emulsifiers, e.g. Pemulen types (TR-1, TR-2) from Goodrich;
> Polyalkylenglycole sowie> Polyalkylene glycols as well
> Glycerincarbonat.> Glycerine carbonate.
> Ethylenoxidanlagerungsprodukte> Ethylene oxide addition products
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 Alkoxylierungsgrad dem Verhältnis der Stoffmengen von Ethylenoxid und/ oder Propylenoxid und Substrat, mit denen die Anlagerungsreaktion durchgeführt wird, entspricht. Ci2/ιs-Fettsäuremono- und -diester von Anlagerungsprodukten von Ethylenoxid an Glycerin sind 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 are homolog mixtures whose average degree of alkoxylation corresponds to the ratio of the amounts of ethylene oxide and / or propylene oxide and substrate with which the addition reaction is carried out. Ci2 / ιs fatty acid monoesters and diesters of adducts of ethylene oxide with glycerol are known as refatting agents for cosmetic preparations.
Alkyl- und/oder AlkenyloligoglvkosideAlkyl and / or alkenyl oligoglycosides
Alkyl- und/oder Alkenylollgoglycoside, ihre Herstellung und ihre Verwendung sind aus dem Stand der Technik bekannt. Ihre Herstellung erfolgt insbesondere durch Umsetzung von Glucose oder Oligosacchariden mit primären Alkoholen mit 8 bis 18 Kohlenstoffatomen. Bezüglich des Glycosid- restes gilt, daß sowohl Monoglycoside, bei denen ein cyclischer Zuckerrest glycosidisch an den Fettalkohol gebunden ist, als auch oligomere Glycoside mit einem Oligomerisationsgrad bis vorzugsweise etwa 8 geeignet sind. Der Ollgomerisierungsgrad ist dabei ein statistischer Mittelwert, dem eine für solche technischen Produkte übliche Homologenverteilung zugrunde liegt.Alkyl and / or alkenylollgoglycosides, their preparation and their use are known from the prior art. They are produced in particular by reacting glucose or oligosaccharides with primary alcohols with 8 to 18 carbon atoms. With regard to the glycoside residue, both monoglycosides in which a cyclic sugar residue is glycosidically bound to the fatty alcohol and oligomeric glycosides with a degree of oligomerization of up to about 8 are suitable. The degree of olomerization is a statistical mean value which is based on a homolog distribution customary for such technical products.
PartialglvceridePartialglvceride
Typische Beispiele für geeignete Partialglyceride sind Hydroxystearinsäuremonoglycerid, Hydroxy- stearinsäurediglycerid, Isostearinsäuremonoglycerid, Isostearinsäurediglycerid, Ölsäuremonogly- cerid, Ölsäurediglycerid, Ricinolsäuremoglycerid, Ricinolsäurediglycerid, Linolsäuremonoglycerid, Linolsäurediglycerid, Linolensäuremonoglycerid, Linolensäurediglycerid, Erucasäuremonoglycerid, Erucasäurediglycerid, Weinsäuremonoglycerid, Weinsäurediglycerid, Citronensäuremonoglycerid, Citronendiglycerid, Äpfelsäuremonoglycerid, Äpfelsäurediglycerid 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.Typical examples of suitable partial glycerides are hydroxystearic acid monoglyceride, stearic acid diglyceride hydroxy, isostearic acid, Isostearinsäurediglycerid, Ölsäuremonogly- cerid, oleic acid diglyceride, Ricinolsäuremoglycerid, Ricinolsäurediglycerid, Linolsäuremonoglycerid, Linolsäurediglycerid, Linolensäuremonoglycerid, Linolensäurediglycerid, Erucasäuremonoglycerid, Erucasäurediglycerid, Weinsäuremonoglycerid, Weinsäurediglycerid, Citronensäuremonoglycerid, Citronendiglycerid, Äpfelsäuremonoglycerid, 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.
Sorbitanestersorbitan
Als Sorbitanester kommen Sorbitanmonoisostearat, Sorbitansesquiisostearat, Sorbitan- diisostearat, Sorbitantriisostearat, Sorbitanmonooleat, Sorbitansesquioleat, Sorbitan-dioleat, Sor- bitantrioleat, Sorbitanmonoerucat, Sorbitansesquierucat, Sorbitandierucat, Sorbitantrierucat, Sor- bitanmonoricinoleat, Sorbitansesquiricinoleat, Sorbitandiricinoleat, Sorbitantriricinoleat, Sorbitan- monohydroxystearat, Sorbitansesquihydroxystearat, Sorbitandihydroxystearat, Sorbitantrihydro- xystearat, Sorbitanmonotartrat, Sorbitansesq u i-tartrat, Sorbitanditartrat, Sorbitantritartrat, Sorbi- tanmonocitrat, Sorbitansesquicitrat, Sorbitandicitrat, Sorbitantricitrat, Sorbitanmonomaleat, Sorbi- tansesquimaleat, 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.As sorbitan sorbitan, sorbitan sesquiisostearate, sorbitan come diisostearate, sorbitan triisostearate, sorbitan monooleate, sorbitan dioleate, bitantrioleat sorting, Sorbitanmonoerucat, Sorbitansesquierucat, Sorbitandierucat, Sorbitantrierucat, sorting bitanmonoricinoleat, Sorbitansesquiricinoleat, Sorbitandiricinoleat, Sorbitantriricinoleat, sorbitan monohydroxystearat, Sorbitansesquihydroxystearat, Sorbitandihydroxystearat , Sorbitan trihydroxystearate, sorbitan monotartrate, sorbitan sesq u i-tartrate, sorbitan ditartrate, sorbitan tritartrate, sorbi- Tan monocitrate, sorbitan sesquicitrate, sorbitan dicitrate, sorbitan tricitrate, sorbitan monomaleate, sorbitan sesquimaleate, sorbitan dimaleate, sorbitan trimaleate and their technical mixtures. Addition products of 1 to 30, preferably 5 to 10, mol of ethylene oxide onto the sorbitan esters mentioned are also suitable.
> Polyglycerinester> Polyglycerol esters
Typische Beispiele für geeignete Polyglycerinester sind Polyglyceryl-2 Dipolyhydroxystearate (De- hymuls® PGPH), Polyglycerin-3-Diisostearate (Lameform® TGI), Polyglyceryl-4 Isostearate (Iso- lan® Gl 34), Polyglyceryl-3 Oleate, Diisostearoyl Polyglyceryl-3 Diisostearate (Isolan® PDI), Po- lyglyceryl-3 Methylglucose Distearate (Tego Care® 450), Polyglyceryl-3 Beeswax (Gera Bellina®), Polyglyceryl-4 Caprate (Polyglycerol Caprate T2010/90), Polyglyceryl-3 Cetyl Ether (Chime- xane® NL), Polyglyceryl-3 Distearate (Cremophor® GS 32) und Polyglyceryl Polyricinoleate (Ad- mul® 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 dipolyhydroxystearates (Dehymuls® PGPH), polyglycerol-3-diisostearates (Lameform® TGI), polyglyceryl-4 isostearates (Isolan® Gl 34), polyglyceryl-3 oleates, diisostearoyl polyglyceryl polyglyceryl 3 diisostearates (Isolan® PDI), polyglyceryl-3 methylglucose distearate (Tego Care® 450), polyglyceryl-3 beeswax (Gera 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.
Amphothere und kationische EmulgatorenAmphoteric and cationic emulsifiers
Weiterhin können als Emulgatoren zwitterionische Tenside verwendet werden. Als zwitterionische Tenside werden solche oberflächenaktiven Verbindungen bezeichnet, die im Molekül mindestens eine quartäre Ammoniumgruppe und mindestens eine Carboxylat- und eine Sulfonatgruppe tragen. Besonders geeignete zwitterionische Tenside sind die sogenannten Betaine wie die N-Alkyl- N,N-dimethylammoniumglycinate, beispielsweise das Kokosalkyldimethylammoniumglycinat, N- Acylaminopropyl-N,N-dimethylammonium-glycinate, beispielsweise das Kokosacyl- aminopropyldimethyl-ammoniumglycinat, und 2-Alkyl-3-carboxylmethyl-3-hydroxyethylimidazoline mit jeweils 8 bis 18 C-Atomen in der Alkyl- oder Acylgruppe sowie das Kokosacylaminoethyl- hydroxyethylcarboxymethylglycinat. Besonders bevorzugt ist das unter der CTFA-Bezeichnung Cocamidopropyl Betaine bekannte Fettsäureamid-Derivat. Ebenfalls geeignete Emulgatoren sind ampholytische Tenside. Unter ampholytischen Tensiden werden solche oberflächenaktiven Verbindungen verstanden, die außer einer Cs -Alkyl- oder Acylgruppe im Molekül mindestens eine freie Aminogruppe und mindestens eine -COOH- oder -Sθ3H-Gruppe enthalten und zur Ausbildung innerer Salze befähigt sind. Beispiele für geeignete ampholytische Tenside sind N- Alkylglycine, N-Alkylpropion-säuren, N-Alkylaminobuttersäuren, N-Alkyliminodipropionsäuren, N- Hydroxyethyl-N-alkylamidopropylglycine, N-Alkyltaurine, N-Alkylsarcosine, 2-Alkylaminopropion- säuren und Alkylaminoessigsäuren mit jeweils etwa 8 bis 18 C-Atomen in der Alkylgruppe.. Besonders bevorzugte ampholytische Tenside sind das N-Kokosalkylaminopropionat, das Kokosa- cylaminoethylaminopropionat und das Ci2/i8-Acylsarcosin. Schließlich kommen auch Kationtenside als Emulgatoren in Betracht, wobei solche vom Typ der Esterquats, vorzugsweise methylquater- nierte Difettsäuretriethanolaminester-Salze, besonders bevorzugt sind.Zwitterionic surfactants can also be used as emulsifiers. Zwitterionic surfactants are surface-active compounds that contain at least one quaternary ammonium group and at least one carboxylate and one sulfonate group in the molecule. Particularly suitable zwitterionic surfactants are the so-called betaines such as the N-alkyl-N, N-dimethylammonium glycinate, for example coconut alkyldimethylammonium glycinate, N-acylaminopropyl-N, N-dimethylammonium glycinate, for example coconut acylaminopropyldimethylammonium glycinate, and 2-alkyl-3 -carboxylmethyl-3-hydroxyethylimidazolines each having 8 to 18 carbon atoms in the alkyl or acyl group and the coconut acylaminoethyl hydroxyethylcarboxymethylglycinate. This is particularly preferred under the CTFA name Cocamidopropyl betaine known fatty acid amide derivative. Suitable emulsifiers are ampholytic surfactants. Ampholytic surfactants are surface-active compounds which, in addition to a Cs-alkyl or acyl group, contain at least one free amino group and at least one -COOH or -Sθ3H group in the molecule and are capable of forming internal salts. Examples of suitable ampholytic surfactants are N-alkylglycines, N-alkylpropionic acids, N-alkylaminobutyric acids, N-alkyliminodipropionic acids, N-hydroxyethyl-N-alkylamidopropylglycines, N-alkyltaurines, N-alkylsarcosines, 2-alkylaminopropionic acids and alkylaminoacetic acids, each with about 8 to 18 carbon atoms in the alkyl group. Particularly preferred ampholytic surfactants are N-cocoalkylaminopropionate, cocacylaminoethylaminopropionate and Ci2 / i8-acylsarcosine. Finally, cationic surfactants are also suitable as emulsifiers, those of the esterquat type, preferably methyl-quaternized difatty acid triethanolamine ester salts, being particularly preferred.
Fette und WachseFats and waxes
Typische Beispiele für Fette sind Glyceride, d.h. feste oder flüssige pflanzliche oder tierische Produkte, die im wesentlichen aus gemischten Glycerinestern höherer Fettsäuren bestehen, als Wachse kommen u.a. natürliche Wachse, wie z.B. Candelillawachs, Carnaubawachs, Japanwachs, Espartograswachs, Korkwachs, Guarumawachs, Reiskeimölwachs, Zuckerrohrwachs, Ouricurywachs, Montanwachs, Bienenwachs, Schellackwachs, Walrat, Lanolin (Wollwachs), Bürzelfett, Ceresin, Ozokerit (Erdwachs), Petrolatum, Paraffinwachse, Mikrowachse; chemisch modifizierte Wachse (Hartwachse), wie z.B. Montanesterwachse, Sasolwachse, hydrierte Jojobawachse sowie synthetische Wachse, wie z.B. Poly- alkylenwachse und Polyethylenglycolwachse in Frage. Neben den Fetten kommen als Zusatzstoffe auch fettähnliche Substanzen, wie Lecithine und Phospholipide in Frage. Unter der Bezeichnung Le- cithine versteht der Fachmann diejenigen Glycero-Phospholipide, die sich aus Fettsäuren, Glycerin, Phosphorsäure und Cholin durch Veresterung bilden. Lecithine werden in der Fachwelt daher auch häufig als Phosphatidylcholine (PC). Als Beispiele für natürliche Lecithine seien die Kephaline genannt, die auch als Phosphatidsäuren bezeichnet werden und Derivate der 1 ,2-Diacyl-sn-glycerin-3- phosphorsäuren darstellen. Dem gegenüber versteht man unter Phospholipiden gewöhnlich Mono- und vorzugsweise Diester der Phosphorsäure mit Glycerin (Glycerinphosphate), die allgemein zu den Fetten gerechnet werden. Daneben kommen auch Sphingosine bzw. Sphingolipide in Frage.Typical examples of fats are glycerides, i.e. Solid or liquid vegetable or animal products, which consist essentially of mixed glycerol esters of higher fatty acids, come as waxes, among others. natural waxes, e.g. Candelilla wax, carnauba wax, japan wax, esparto grass wax, cork wax, guaruma wax, rice germ oil wax, sugar cane wax, ouricury wax, montan wax, beeswax, shellac wax, walnut, lanolin (wool wax), pretzel fat, ceresin, ozokerite (earth wax), petrolatum, paraffin waxes, micro waxes chemically modified waxes (hard waxes), e.g. Montanester waxes, Sasol waxes, hydrogenated jojoba waxes and synthetic waxes, such as Polyalkylene waxes and polyethylene glycol waxes in question. In addition to fats, fat-like substances such as lecithins and phospholipids can also be used as additives. The term “lecithins” is understood by the person skilled in the art to mean those glycerophospholipids which form from fatty acids, glycerol, phosphoric acid and choline by esterification. Lecithins are therefore often used in the professional world as phosphatidylcholines (PC). Examples of natural lecithins are the cephalins, which are also referred to as phosphatidic acids and are derivatives of 1,2-diacyl-sn-glycerol-3-phosphoric acids. In contrast, phospholipids are usually understood to be mono- and preferably diesters of phosphoric acid with glycerol (glycerol phosphates), which are generally classed as fats. In addition, sphingosines or sphingolipids are also suitable.
Perlglanzwachsepearlescent
Als Perlglanzwachse kommen beispielsweise in Frage: AI ky leng lyco lester, speziell Ethylenglycoldi- stearat; Fettsäurealkanolamide, speziell Kokosfettsäurediethanolamid; Partialglyceride, speziell Stea- rinsäuremonoglycerid; 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 mit 12 bis 22 Kohlenstoffatomen und/oder Polyolen mit 2 bis 15 Kohlenstoffatomen und 2 bis 10 Hydroxylgruppen sowie deren Mischungen.Pearlescent waxes that can be used are, for example: Al ky leng lycolester, especially ethylene glycol distearate; Fatty acid alkanolamides, especially coconut fatty acid diethanolamide; Partial glycerides, especially steak rinsäuremonoglycerid; 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 with 12 to 22 carbon atoms and / or polyols with 2 to 15 carbon atoms and 2 to 10 hydroxyl groups and mixtures thereof.
Konsistenzgeber und VerdickungsmittelConsistency 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 Hydroxyfett- säuren in Betracht. Bevorzugt ist eine Kombination dieser Stoffe mit Alkylollgoglucosiden und/oder Fettsäure-N-methylglucamiden gleicher Kettenlänge und/oder Polyglycerinpoly-12-hydroxystearaten. Geeignete Verdickungsmittel sind beispielsweise Aerosil-Typen (hydrophile Kieselsäuren), Polysaccha- ride, insbesondere Xanthan-Gum, Guar-Guar, Agar-Agar, Alginate und Tylosen, Carboxymethyl- cellulose und Hydroxyethyl- und Hydroxypropylcellulose, ferner höhermolekulare Polyethylenglycolmo- no- 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 Al- lied Colloids), Polyacrylamide, Polymere, Polyvinylalkohol und Poly vinylpyrrolidon . 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 hydroxyfatty alcohols with 12 to 22 and preferably 16 to 18 carbon atoms and also partial glycerides, fatty acids or hydroxyfatty acids. A combination of these substances with alkylollgoglucosides 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, guar guar, 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, (eg 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 Poly vinyl pyrrolidone. 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 polyethoxy- lierte oder acylierte Lanolin- und Lecithinderivate, Polyolfettsäureester, Monoglyceride und Fettsäureal- kanolamide verwendet werden, wobei die letzteren gleichzeitig als Schaumstabilisatoren dienen. StabilisatorenSubstances such as, for example, lanolin and lecithin, and also 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. stabilizers
Als Stabilisatoren können Metallsalze von Fettsäuren, wie z.B. Magnesium-, Aluminium- und/oder Zinkstearat bzw. -ricinoleat eingesetzt werden.Metal salts of fatty acids, such as e.g. Magnesium, aluminum and / or zinc stearate or ricinoleate are used.
Polymerepolymers
Geeignete kationische Polymere sind beispielsweise kationische Cellulosederivate, wie z.B. eine qua- ternierte Hydroxyethylcellulose, die unter der Bezeichnung Polymer JR 400® von Amerchol erhältlich ist, kationische Stärke, Copolymere von Diallylammoniumsalzen und Acrylamiden, quatemierte Vinyl- pyrrolidon/Vinylimidazol-Polymere, wie z.B. Luviquat® (BASF), Kondensationsprodukte von Poly- glycolen und Aminen, quatemierte Kollagenpolypeptide, wie beispielsweise Lauryldimonium Hydro- xypropyl Hydrolyzed Collagen (Lamequat®L/Grünau), quatemierte Weizenpolypeptide, Polyethyleni- min, kationische Siliconpolymere, wie z.B. Amodimethicone, Copolymere der Adipinsäure und Di- methylaminohydroxypropyldiethylentriamin (Cartaretine®/Sandoz), Copolymere der Acrylsäure mit Dimethyl-diallylammoniumchlorid (Merquat® 550/Chemviron), Polyaminopolyamide, sowie deren vernetzte wasserlöslichen Polymere, kationische Chitinderivate wie beispielsweise quaterniertes Chitosan, gegebenenfalls mikrokristallin verteilt, Kondensationsprodukte aus Dihalogenalkylen, wie z.B. Dibrom- butan 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, quatemierte 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, e.g. a quaternized hydroxyethyl cellulose available under the name Polymer JR 400® from Amerchol, cationic starch, copolymers of diallylammonium salts and acrylamides, quaternized vinylpyrrolidone / vinylimidazole polymers such as e.g. Luviquat® (BASF), condensation products of polyglycols and amines, quaternized collagen polypeptides, such as lauryldimonium hydroxypropyl hydrolyzed collagen (Lamequat®L / Grünau), quaternized wheat polypeptides, polyethyleneimine, cationic silicone polymers, such as e.g. Amodimethicones, copolymers of adipic acid and dimethylaminohydroxypropyldiethylenetriamine (Cartaretine® / Sandoz), copolymers of acrylic acid with dimethyldiallylammonium chloride (Merquat® 550 / Chemviron), polyaminopolyamides, as well as their crosslinked water-soluble polymers, cationic chitin derivatives, such as quanernized, optionally quaternized, Condensation products from dihaloalkylene, such as Dibromobutane with bisdialkylamines, e.g. Bis-dimethylamino-1,3-propane, cationic guar gum, e.g. Jaguar® CBS, Jaguar® C-17, Jaguar® C-16 from Celanese, quaternized ammonium salt polymers, e.g. Mirapol® A-15, Mirapol® AD-1, Mirapol® AZ-1 from Miranol.
Als anionische, zwitterionische, amphotere und nichtionische Polymere kommen beispielsweise Vinyl- acetat/Crotonsäure-Copolymere, Vinylpyrrolidon/Vinylacrylat-Copolymere, Vinylacetat/Butylmaleat/ Isobomylacrylat-Copolymere, Methylvinylether/Maleinsäureanhydrid-Copolymere und deren Ester, un- vernetzte und mit Polyolen vernetzte Polyacrylsäuren, Acrylamidopropyltrimethylammoniumchlorid/ Acrylat-Copolymere, Octylacrylamid/Methylmeth-acrylat/tert.Butylaminoethylmethacrylat/2-Hydroxypro- pylmethacrylat-Copolymere, Polyvinylpyrrolidon, Vinylpyrrolidon/Vinylacetat-Copolymere, Vinylpyrroli- don/ Dimethylaminoethylmethacrylat/Vinylcaprolactam-Terpolymere sowie gegebenenfalls derivatisierte Celluloseether und Silicone in Frage.Anionic, zwitterionic, amphoteric and nonionic polymers include, for example, vinyl acetate / crotonic acid copolymers, vinylpyrrolidone / vinyl acrylate copolymers, vinyl acetate / butyl maleate / isobomylacrylate copolymers, methyl vinyl ether / maleic anhydride copolymers and their crosslinked polyols and their esters, polyols and their polyols , Acrylamidopropyltrimethylammonium chloride / acrylate copolymers, octylacrylamide / methyl methacrylate / tert.butylaminoethyl methacrylate / 2-hydroxypropyl methacrylate copolymers, polyvinylpyrrolidone, vinylpyrrolidone / vinyl acetate copolymers, vinylpyrrolidone / dimethylamino-methyl-acrylate and acrylate-vinylamine / vinyl acrylate-methacrylate, if appropriate, and also vinyl-pyridolidate / dimethylamino-methyl-methacrylate ,
Siliconverbindungensilicone compounds
Geeignete Siliconverbindungen sind beispielsweise Dimethylpolysiloxane, Methylphenylpolysiloxane, cyclische Silicone sowie amino-, fettsäure-, alkohol-, polyether-, epoxy-, fluor-, glykosid- und/oder al- kylmodifizierte Siliconverbindungen, die bei Raumtemperatur sowohl flüssig als auch harzförmig vor- liegen können. Weiterhin geeignet sind Simethicone, bei denen es sich um Mischungen aus Dimethico- nen mit einer durchschnittlichen Kettenlänge von 200 bis 300 Dimethylsiloxan-Einheiten und hydrierten Silicaten handelt.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 are both liquid and resinous at room temperature. can lie. Simethicones, which are mixtures of dimethicones with an average chain length of 200 to 300 dimethylsiloxane units and hydrogenated silicates, are also suitable.
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 und Vitaminkomplexe zu verstehen.Examples of biogenic active substances are 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, pseudo-leeroceramides, essential extracts, plant extracts Understand vitamin complexes.
Hydrotropehydrotropes
Zur Verbesserung des Fließverhaltens können ferner Hydrotrope, wie beispielsweise Ethanol, Isopro- pylalkohol, 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 funktioneile 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 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-1 ,3-propandiol. Konservierungsmittel> Dialcohol amines, such as diethanolamine or 2-amino-1, 3-propanediol. preservative
Als Konservierungsmittel eignen sich beispielsweise Phenoxyethanol, Formaldehydiösung, 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 Regulation.
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.-Bu- tylcyclohexylacetat, Linalylacetat, Dimethylbenzylcarbinylacetat, Phenylethylacetat, Linalylbenzoat, Benzylformiat, Ethylmethylphenylglycinat, Allylcyclohexylpropionat, Styrallylpropionat und Benzylsa- licylat. Zu den Ethern 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-lsomethylionon und Me- thylcedrylketon, zu den Alkoholen Anethol, Citronellol, Eugenol, Isoeugenol, Geraniol, Linalool, Pheny- lethylalkohol 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, Galbanu- möl, Labolanumöl und Lavandinöl. Vorzugsweise werden Bergamotteöl, Dihydromyrcenol, Lilial, Lyral, Citronellol, Phenylethylalkohol, α-Hexylzimtaldehyd, Geraniol, Benzylaceton, Cyclamenaldehyd, Linalool, Boisambrene Forte, Ambroxan, Indol, Hedione, Sandelice, Citronenöl, Mandarinenöl, Orangenöl, Allylamylglycolat, Cyclovertal, Lavandinöl, Muskateller Salbeiöl, ß-Damascone, Geraniumöl Bourbon, Cyclohexylsalicylat, Vertofix Coeur, Iso-E-Super, Fixolide NP, Evernyl, Iraldein gamma, Phenylessig- säure, Geranylacetat, Benzylacetat, Rosenoxid, Romilllat, Irotyl und Floramat allein oder in Mischungen, eingesetzt. Als Aromen kommen beispielsweise Pfefferminzöl, Krauseminzöl, Anisöl, Sternanisöl, Kümmelöl, Eukalyptusöl, Fenchelöl, Citronenöl, Wintergrünöl, Nelkenöl, Menthol und dergleichen in Frage.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 methylphenylglycinate, allylcyclohexyl benzylatepylpropionate, allyl cyclohexyl propyl pionate. The ethers include, for example, benzyl ethyl ether, the aldehydes include, for example, the linear alkanals having 8 to 18 carbon atoms, citral, citronellal, citronellyloxyacetaldehyde, cyclamenaldehyde, hydroxycitronellal, lilial and bourgeonal, and the ketones include, for example, the jonones, α-isomethylionone and methylcedryl ketone the alcohols anethole, 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. Essential oils of lower volatility, which are mostly used as aroma components, are also 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-hexyl cinnamaldehyde, geraniol, benzylacetone, cyclamenaldehyde, linalool, boisambrene forte, ambroxan, indole, hedione, sandelice, lemon oil, mandarin oil, lavender oil, orange glycolate, almond glycol, alanol glycol, alanol oil, alanol glycolate, alanol glycolate, alanol glycolate, alanol glycolate, alanol glycolate, alanol glycolate, alanol glycolate, alanecalcolate, orange oil, alanol glycolate, alanol glycolate, alanecalcolate, orange oil, alanol glycolate, alanol glycolate, alanecalcolate, orange oil, alanecalcolate, orange oil, aldolate, lamellar oil, orange oil, orange oil, orange oil, aldolate, lemon oil, orange oil, orange oil oil, orange oil oil, alanecalcone oil, orange oil, alanecalcone oil Sage oil, ß-damascone, geranium oil bourbon, cyclohexyl salicylate, Vertofix Coeur, Iso-E-Super, Fixolide NP, evernyl, iraldein gamma, phenylacetic acid, geranyl acetate, benzyl acetate, rose oxide, romilllate, irotyl and floramate alone or in mixtures. 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. Beispiele sind Kochenillerot A (C.l. 16255), Patentblau V (C.1.42051), Indigotin (C.1.73015), Chlorophyllin (C.1.75810), Chinolingelb (C.I.47005), Titandioxid (C.1.77891), Indanthrenblau RS (C.l. 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 which are suitable and approved for cosmetic purposes. Examples are Kochillerot A (Cl 16255), patent blue V (C.1.42051), indigotine (C.1.73015), chlorophylline (C.1.75810), quinoline yellow (CI47005), titanium dioxide (C.1.77891), indanthrene blue RS (Cl 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.
Der Gesamtanteil der Hilfs- und Zusatzstoffe kann 1 bis 50, vorzugsweise 5 bis 40 Gew.-% - bezogen auf die Mittel - betragen. Die Herstellung der Mittel kann durch übliche Kalt - oder Heißprozesse erfolgen; vorzugsweise arbeitet man nach der Phaseninversionstemperatur-Methode. The total proportion of auxiliaries and additives can be 1 to 50, preferably 5 to 40,% by weight, based on the composition. The agents can be produced by customary cold or hot processes; the phase inversion temperature method is preferably used.
BeispieleExamples
Blätter des Olivenbaumes (Olea europaea) wurden gesammt, getrocknet, gemahlen und durch ein 55- 60 Vol. % Ethanol/Wasser-Gemisch bei 60°C über 4 Stunden extrahiert. Das Eluat wurde getrocknet, gemahlen und gesiebt und auf einen Gehalt von ungefähr 20 Gew.% Oleuropein eingestellt.Leaves of the olive tree (Olea europaea) were collected, dried, ground and extracted by a 55-60 vol.% Ethanol / water mixture at 60 ° C. for 4 hours. The eluate was dried, ground and sieved and adjusted to a content of approximately 20% by weight oleuropein.
Zur Bestimmung der antimikrobiellen Wirksamkeit wurde ein Agardiffusionstest durchgeführt.An agar diffusion test was carried out to determine the antimicrobial activity.
Agardiffusionstestagar diffusion test
Testkeime:Test germs:
1. Corynebacterium (C.) minutissimum ATCC 23348 1 ,5 x 103 KBE/ml1. Corynebacterium (C.) minutissimum ATCC 23348 1, 5 x 10 3 CFU / ml
2. Staphylococcus (S.) epidermidis ATCC 12228 2,5 x 103 KBE/ml2. Staphylococcus (S.) epidermidis ATCC 12228 2.5 x 10 3 CFU / ml
3. Propionibacterium (P.) acnes ATCC 11829 3,1 x 103 «BE/ml3. Propionibacterium (P.) acnes ATCC 11829 3.1 x 103 "BE / ml
4. Malassezia (M.) furfur DSM 6171 1 ,9 x 103 KBE/ml4. Malassezia (M.) furfur DSM 6171 1.9 x 103 CFU / ml
Herstellung Testkeimsuspensionen (aerobe Bakterien):Production of test germ suspensions (aerobic bacteria):
Die Testkeime wurden auf Columbia-Blut-Agar (bioMerieux Art. 43049) subkultiviert. Mittels Tupfer wurden soviele Kolonien in NaCI-Peptonpuffer homogenisiert, dass die Trübung dem McFarland Standard 1,0 entsprach.The test germs were subcultured on Columbia blood agar (bioMerieux Art. 43049). Sufficient colonies were homogenized in NaCl peptone buffer using a swab so that the turbidity corresponded to the McFarland Standard 1.0.
Herstellung Testkeimsuspensionen (anaerobe Bakterien):Production of test germ suspensions (anaerobic bacteria):
Die Testkeime wurden auf Schaedler-Agar (bioMerieux Art. 43273) subkultiviert. Mittels Tupfer wurden soviele Kolonien in NaCI-Peptonpuffer homogenisiert, dass die Trübung dem McFarland Standard 1 ,0 entsprach.The test germs were subcultured on Schaedler agar (bioMerieux Art. 43273). Sufficient colonies were homogenized in NaCl peptone buffer using a swab so that the turbidity corresponded to the McFarland Standard 1.0.
Herstellung Testkeimsuspensionen (Hefen und Schimmelpilze):Production of test germ suspensions (yeast and mold):
Die Testkeime wurden auf Sabouraud-Agar HLT (Merck, Art. 18364) subkultiviert. Mittels Tupfer wurden soviele Kolonien in NaCI-Peptonpuffer homogenisiert, dass die Trübung dem McFarland Standard 1,0 entsprach.The test germs were subcultured on Sabouraud agar HLT (Merck, Art. 18364). Sufficient colonies were homogenized in NaCl peptone buffer using a swab so that the turbidity corresponded to the McFarland Standard 1.0.
Probenvorbereitung:Sample preparation:
Eine Testkonzentration von 5 Gew.% Olivenbaumblätterextrakt (Herbalia®Olive - Cognis Iberia S.L., Poligono San Vicente, 08755 Castellbisbal, Barcelona (Spain)) wurde durch Einwiegen von 0,5 g Trockenextrakt und Lösen ad 10 ml mit 15 Vol.% Ethanol (Merck, Art. 100971) eingestellt. Kontrollen:A test concentration of 5% by weight of olive tree leaf extract (Herbalia®Olive - Cognis Iberia SL, Poligono San Vicente, 08755 Castellbisbal, Barcelona (Spain)) was obtained by weighing out 0.5 g of dry extract and dissolving to 10 ml with 15% by volume of ethanol ( Merck, Art. 100971). controls:
K1 Testblättchen unbeimpftK1 test leaves unvaccinated
K2 Testblättchen + 10 resp. 20 μl 15 Vol.% EthanolK2 test papers + 10 resp. 20 ul 15 vol% ethanol
Inkubationsbedingungen:incubation Conditions:
Für jeden Ansatz wurden 3 Testplättchen angelegt. Die Agarplatten wurden3 test plates were created for each batch. The agar plates were
18 h bei 36°C Keim 1 , 218 h at 36 ° C germ 1, 2
72 h bei 36°C anaerob Keim 372 h at 36 ° C anaerobic germ 3
72 h bei 30°C Keim 4 inkubiert.Incubated for 72 h at 30 ° C germ 4.
TestdurchführungTest procedure
Die Testkeime wurden 2%ig mit dem entsprechenden Testmedium (s.u.) homogenisiert. 15 ml davon wurden in Petrischalen gegossen.The test germs were homogenized 2% with the appropriate test medium (see below). 15 ml of this was poured into petri dishes.
Müller Hinton-Agar Merck, Art. 5437 Keim 1 , 2Müller Hinton-Agar Merck, Art. 5437 Germ 1, 2
Wilkens Chalgren Oxoid, Art. CM 643 Keim 3Wilkens Chalgren Oxoid, Art. CM 643 Germ 3
PIT - Medium Keim 4PIT - medium germ 4
(Malz Agar Merck Art. 5398, Ochsengalle 3756, Tween 40822185 und Monoolein Fluka Art. 49960)(Malt Agar Merck Art. 5398, Ochsengalle 3756, Tween 40822185 and Monoolein Fluka Art. 49960)
Nach Erstarren und Trocknung der Platten wurden 5 sterile Testplättchen (6mm Durchmesser, BioMerieux, Art. 54991) ausgelegt (3 x Probe, 2 x Kontrolle). Es wurden je Probe 2 Ansätze durchgeführt: Ansatz 1 mit 10 μl, Ansatz 2 mit 20 μl. Nach Inkubation wurden die Hemmhofdurchmesser [mm] ausgemessen.After solidification and drying of the plates, 5 sterile test plates (6mm diameter, BioMerieux, Art. 54991) were laid out (3 x sample, 2 x control). Two batches were carried out for each sample: batch 1 with 10 μl, batch 2 with 20 μl. After incubation, the inhibition zone diameters [mm] were measured.
ErgebnisseResults
Tabelle 1 : Antimikrobielle Aktivität von OlivenbaumblätterextraktTable 1: Antimicrobial activity of olive tree leaf extract
Insbesondere bei einer Ansatzgröße von 20 μl werden die Mikroorganismen vom Olivenbaumblätter- extrakt deutlich gehemmt. Staphylococcus epidermidis unterliegt der Hemmung bereits bei sehr geringen Probekonzentrationen. Especially with a batch size of 20 μl, the microorganisms from the olive tree leaf extract are significantly inhibited. Staphylococcus epidermidis is subject to inhibition even at very low sample concentrations.
Die nachfolgende Tabelle 2 enthält eine Reihe von Formulierungsbeispiele mit Olivenbaumblätterex- trakt als antimikrobielles Agens.Table 2 below contains a number of formulation examples with olive tree leaf extract as an antimicrobial agent.
Tabelle 2:Table 2:
Handgeschirrspülmittel - FormulierungsbeispieleHand dishwashing liquid - formulation examples
Tabelle 3: Modell-Rezeptur- HandgeschirrspülmittelTable 3: Model formulation - hand dishwashing liquid
Claims
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU2003227054A AU2003227054A1 (en) | 2002-03-22 | 2003-03-13 | Use of olive tree extracts in detergents, rinsing agents and cleaning agents |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10213031A DE10213031A1 (en) | 2002-03-22 | 2002-03-22 | Use of extracts from the olive tree in detergents, dishwashing detergents and cleaning agents |
| DE10213031.0 | 2002-03-22 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO2003079794A1 true WO2003079794A1 (en) | 2003-10-02 |
Family
ID=27798119
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/EP2003/002569 Ceased WO2003079794A1 (en) | 2002-03-22 | 2003-03-13 | Use of olive tree extracts in detergents, rinsing agents and cleaning agents |
Country Status (3)
| Country | Link |
|---|---|
| AU (1) | AU2003227054A1 (en) |
| DE (1) | DE10213031A1 (en) |
| WO (1) | WO2003079794A1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB2459188A (en) * | 2008-04-16 | 2009-10-21 | Syntopix Ltd | Alkyl sulfates and alkyl sulfonates for use as antibacterial agents |
| ITCT20100010A1 (en) * | 2010-06-03 | 2011-12-04 | Labiochem S A S Di Mazzotta A & C | PREPARATION OF A EXTRACT RICH IN POLYPHENOLS AND A SOLID FRACTION FROM WATERS OF VEGETATION OF THE OLIVES AND ITS PHARMACEUTICAL, COSMETIC AND FOOD USE. |
| EP2687090A3 (en) * | 2005-11-14 | 2014-02-19 | Solvay USA Inc. | Agricultural adjuvant compostions, pesticide compositions, and methods for using such compositions |
| WO2015136195A1 (en) * | 2014-03-13 | 2015-09-17 | Centre National De La Recherche Scientifique - Cnrs | Method for reusing deciduous leaves, from an arborescent ligneous plant, for the phytopharmaceutical industry |
| CN115487114A (en) * | 2022-10-12 | 2022-12-20 | 广东粤港澳大湾区黄埔材料研究院 | Antibacterial peptide composition, acne-removing cream containing antibacterial peptide composition and preparation method of acne-removing cream |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10251856B4 (en) * | 2002-11-06 | 2006-05-18 | Cognis Ip Management Gmbh | Use of a textile treatment agent |
| DE102012103767A1 (en) * | 2012-04-27 | 2013-10-31 | Chemische Fabrik Budenheim Kg | Use of solubilizate comprising antimicrobial agent, emulsifier and water, as antimicrobial agent which is enclosed in micelles, e.g. for bacteriostatic or germ-reducible treatment of room air, food, objects by applying to object surfaces |
| CN104789383A (en) * | 2015-05-19 | 2015-07-22 | 胡洪梅 | Antibacterial washing liquid |
| EP3354135A1 (en) | 2017-01-31 | 2018-08-01 | CuraSolutions GmbH | Antimicrobial composition with reinforced effect for the treatment of liquids containing water |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001026670A1 (en) * | 1999-10-14 | 2001-04-19 | The Nisshin Oil Mills, Ltd. | Skin-care agents, skin antiaging agents, whitening agents and external skin preparations |
| GB2357968A (en) * | 2000-12-18 | 2001-07-11 | Ciba Sc Holding Ag | Use of hydroxy diphenylethers as disinfectants |
| FR2810887A1 (en) * | 2000-06-29 | 2002-01-04 | Seporga Lab | Cosmetic or dermatological compositions for use in protecting the skin against solar radiation, chemicals and detergents comprise 0.01 to 10 percent of an extract of olive leaves |
| JP2002020305A (en) * | 2000-07-07 | 2002-01-23 | Fukushi Kobo:Kk | Health food, functional food and medicine containing leaf component of plant of genus olea and seed component of plant genus citrus |
| FR2825022A1 (en) * | 2001-05-23 | 2002-11-29 | Seppic Sa | Nontherapeutic treatment of the human or animal body comprises administering or applying olive polyphenols |
-
2002
- 2002-03-22 DE DE10213031A patent/DE10213031A1/en not_active Withdrawn
-
2003
- 2003-03-13 WO PCT/EP2003/002569 patent/WO2003079794A1/en not_active Ceased
- 2003-03-13 AU AU2003227054A patent/AU2003227054A1/en not_active Abandoned
Patent Citations (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001026670A1 (en) * | 1999-10-14 | 2001-04-19 | The Nisshin Oil Mills, Ltd. | Skin-care agents, skin antiaging agents, whitening agents and external skin preparations |
| EP1230926A1 (en) * | 1999-10-14 | 2002-08-14 | The Nisshin Oil Mills, Ltd. | Skin-care agents, skin antiaging agents, whitening agents and external skin preparations |
| FR2810887A1 (en) * | 2000-06-29 | 2002-01-04 | Seporga Lab | Cosmetic or dermatological compositions for use in protecting the skin against solar radiation, chemicals and detergents comprise 0.01 to 10 percent of an extract of olive leaves |
| JP2002020305A (en) * | 2000-07-07 | 2002-01-23 | Fukushi Kobo:Kk | Health food, functional food and medicine containing leaf component of plant of genus olea and seed component of plant genus citrus |
| GB2357968A (en) * | 2000-12-18 | 2001-07-11 | Ciba Sc Holding Ag | Use of hydroxy diphenylethers as disinfectants |
| FR2825022A1 (en) * | 2001-05-23 | 2002-11-29 | Seppic Sa | Nontherapeutic treatment of the human or animal body comprises administering or applying olive polyphenols |
Non-Patent Citations (3)
| Title |
|---|
| DATABASE BIOSIS [online] BIOSCIENCES INFORMATION SERVICE, PHILADELPHIA, PA, US; August 1999 (1999-08-01), BISIGNANO GIUSEPPE ET AL: "On the in-vitro antimicrobial activity of oleuropein and hydroxytyrosol.", XP002245394, Database accession no. PREV199900499655 * |
| DATABASE WPI Section Ch Week 200232, Derwent World Patents Index; Class B04, AN 2002-275343, XP002245395 * |
| JOURNAL OF PHARMACY AND PHARMACOLOGY, vol. 51, no. 8, August 1999 (1999-08-01), pages 971 - 974, ISSN: 0022-3573 * |
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2687090A3 (en) * | 2005-11-14 | 2014-02-19 | Solvay USA Inc. | Agricultural adjuvant compostions, pesticide compositions, and methods for using such compositions |
| GB2459188A (en) * | 2008-04-16 | 2009-10-21 | Syntopix Ltd | Alkyl sulfates and alkyl sulfonates for use as antibacterial agents |
| ITCT20100010A1 (en) * | 2010-06-03 | 2011-12-04 | Labiochem S A S Di Mazzotta A & C | PREPARATION OF A EXTRACT RICH IN POLYPHENOLS AND A SOLID FRACTION FROM WATERS OF VEGETATION OF THE OLIVES AND ITS PHARMACEUTICAL, COSMETIC AND FOOD USE. |
| WO2015136195A1 (en) * | 2014-03-13 | 2015-09-17 | Centre National De La Recherche Scientifique - Cnrs | Method for reusing deciduous leaves, from an arborescent ligneous plant, for the phytopharmaceutical industry |
| FR3018427A1 (en) * | 2014-03-13 | 2015-09-18 | Centre Nat Rech Scient | PROCESS FOR RECOVERING ARBORESCENT PORTABLE PLANT SIDE PLANT SHEETS FOR THE PHYTOPHARMACEUTICAL INDUSTRY |
| US11213033B2 (en) | 2014-03-13 | 2022-01-04 | Agro Innovation International | Method for reusing leaves from arborescent woody plants, for the phytopharmaceutical industry |
| CN115487114A (en) * | 2022-10-12 | 2022-12-20 | 广东粤港澳大湾区黄埔材料研究院 | Antibacterial peptide composition, acne-removing cream containing antibacterial peptide composition and preparation method of acne-removing cream |
| CN115487114B (en) * | 2022-10-12 | 2023-10-03 | 广东粤港澳大湾区黄埔材料研究院 | Antibacterial peptide composition, acne-removing cream containing antibacterial peptide composition and preparation method of acne-removing cream |
Also Published As
| Publication number | Publication date |
|---|---|
| DE10213031A1 (en) | 2003-10-02 |
| AU2003227054A1 (en) | 2003-10-08 |
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