EP3558030A1 - Mélange aromatique destiné à la réduction de l'odeur ou du goût d'amines biogènes - Google Patents

Mélange aromatique destiné à la réduction de l'odeur ou du goût d'amines biogènes

Info

Publication number
EP3558030A1
EP3558030A1 EP16822452.5A EP16822452A EP3558030A1 EP 3558030 A1 EP3558030 A1 EP 3558030A1 EP 16822452 A EP16822452 A EP 16822452A EP 3558030 A1 EP3558030 A1 EP 3558030A1
Authority
EP
European Patent Office
Prior art keywords
acid
trimethylcyclohex
trimethyl
ionone
methyl
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
EP16822452.5A
Other languages
German (de)
English (en)
Inventor
Johannes KIEFL
Uwe Schaefer
Birgit Kohlenberg
Thomas Henze
Stephanie KORTE
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Symrise AG
Original Assignee
Symrise AG
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Symrise AG filed Critical Symrise AG
Publication of EP3558030A1 publication Critical patent/EP3558030A1/fr
Pending legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L5/00—Preparation or treatment of foods or foodstuffs, in general; Food or foodstuffs obtained thereby; Materials therefor
    • A23L5/20—Removal of unwanted matter, e.g. deodorisation or detoxification
    • A23L5/27—Removal of unwanted matter, e.g. deodorisation or detoxification by chemical treatment, by adsorption or by absorption
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
    • A23L27/84—Flavour masking or reducing agents
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
    • A23L27/20—Synthetic spices, flavouring agents or condiments
    • A23L27/205—Heterocyclic compounds
    • A23L27/2054—Heterocyclic compounds having nitrogen as the only hetero atom
    • A—HUMAN NECESSITIES
    • A23—FOODS OR FOODSTUFFS; TREATMENT THEREOF, NOT COVERED BY OTHER CLASSES
    • A23L—FOODS, FOODSTUFFS, OR NON-ALCOHOLIC BEVERAGES, NOT COVERED BY SUBCLASSES A21D OR A23B-A23J; THEIR PREPARATION OR TREATMENT, e.g. COOKING, MODIFICATION OF NUTRITIVE QUALITIES, PHYSICAL TREATMENT; PRESERVATION OF FOODS OR FOODSTUFFS, IN GENERAL
    • A23L27/00—Spices; Flavouring agents or condiments; Artificial sweetening agents; Table salts; Dietetic salt substitutes; Preparation or treatment thereof
    • A23L27/50—Soya sauce
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/22—Heterocyclic compounds, e.g. ascorbic acid, tocopherol or pyrrolidones
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/34—Alcohols
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/35—Ketones, e.g. benzophenone
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/494—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with more than one nitrogen as the only hetero atom
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00—Cosmetics or similar toiletry preparations
    • A61K8/18—Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4973—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom
    • A61K8/498—Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with oxygen as the only hetero atom having 6-membered rings or their condensed derivatives, e.g. coumarin
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0026—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring
    • C11B9/0034—Essential oils; Perfumes compounds containing an alicyclic ring not condensed with another ring the ring containing six carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0042—Essential oils; Perfumes compounds containing condensed hydrocarbon rings
    • C11B9/0046—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings
    • C11B9/0049—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms
    • C11B9/0053—Essential oils; Perfumes compounds containing condensed hydrocarbon rings containing only two condensed rings the condensed rings sharing two common C atoms both rings being six-membered
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0069—Heterocyclic compounds
    • C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
    • C11B9/0076—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing less than six atoms
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0069—Heterocyclic compounds
    • C11B9/0073—Heterocyclic compounds containing only O or S as heteroatoms
    • C11B9/008—Heterocyclic compounds containing only O or S as heteroatoms the hetero rings containing six atoms
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11B—PRODUCING, e.g. BY PRESSING RAW MATERIALS OR BY EXTRACTION FROM WASTE MATERIALS, REFINING OR PRESERVING FATS, FATTY SUBSTANCES, e.g. LANOLIN, FATTY OILS OR WAXES; ESSENTIAL OILS; PERFUMES
    • C11B9/00—Essential oils; Perfumes
    • C11B9/0069—Heterocyclic compounds
    • C11B9/0092—Heterocyclic compounds containing only N as heteroatom

Definitions

  • the present invention relates to flavor compositions and foods.
  • an aroma mixture comprising a first component comprising a molecule selected from the group comprising molecules of the following structure (I):
  • R 1 is selected from hydrogen or methyl
  • R is O or OH, i. Keto or hydroxy group; such as
  • R is selected from methyl, ethyl, propyl, isopropyl or propenyl,
  • nnnnft a single or double bond, wherein allenes or Cumulen- structures are excluded
  • R 4 is selected from hydrogen and propenyl
  • the first and / or second component preferably consists predominantly of the respectively indicated molecules.
  • the term "predominantly consist” means in particular a proportion (in wt / wt) of> 95%, preferably> 97% and most preferably> 99%.
  • the aroma mixture thus comprises at least one biogenic amine.
  • biogenic amines is understood in particular as meaning amines and secondary products which may arise from protein degradation, in particular 2-phenylethylamine, cadaverine, histamine, putrescine, spermidine, spermine, tryptamine, tyramine, indole, skatole, methylamines, dimethylamine, trimethylamine, Acetic acid, propionic acid, 2-methylbutyric acid, 3-methylbutyric acid, 4-methylpentanoic acid, diethylamine,
  • Ethylmethylamine and diethanolamine are usually referred to as amines, here should explicitly apply a deviation from the standard linguistic usage.
  • a food preparation comprising at least one biogenic amine additionally comprising the first and second components as described, wherein the first and second Component independently of one another in the food or food preparation at least in a concentration of> l micrograms / kg.
  • the present invention also relates to the use of a flavoring mixture comprising the first and / or second component for reducing and / or masking the taste and / or odor of biogenic amines. It has been found that in many applications already one component is sufficient to achieve such an effect.
  • the first component contains at least one molecule selected from the group comprising:
  • the second component comprises at least one molecule selected from the group comprising:
  • the compound (19) is a chiral compound, in which case both the individual enantiomers and the racemate are preferred embodiments.
  • the second component is added as a substance.
  • the second component is obtained by treating a precursor of the aroma mixture according to the invention or a composition which contains a precursor of the aroma mixture according to the invention, or by treating a precursor of the food or food preparation according to the invention. This applies mutatis mutandis for the use according to the invention and the inventive
  • the aroma mixture according to the invention, the foodstuffs according to the invention or the food preparation as well as the use according to the invention may comprise further ingredients.
  • ingredients are selected from substances for changing or masking an unpleasant
  • Taste impression and / or to enhance a pleasant taste impression or flavoring agents are preferably selected from the following group: 4-hydroxyflavanones, for example as described in EP 1,258,200-B1, hesperetin as described in EP 2,368,442-Bl or EP 1,909,599-B1, hydroxybenzoic acid amides, for example 2,4-dihydroxybenzoic acid vanillylamide (in particular those as described in WO 2006/024587), 4-hydroxydihydrochalcones (preferably as described in US 2008/0227867 Al and WO 2007/107596), in particular phloretin and davidigenin, hesperetin as disclosed in WO 2007/014879, or extracts from Rubus suavissimus as described in US Provisional Application 61 / 333,435 (Symrise) and based thereon
  • Patent applications 3,7'-dihydroxy-4'-methoxyflavan isomers as described in EP 2,253,226, phyllodulcin isomers or phyllodulcine-containing extracts as described in EP 2,298,084-Bl, l- (2,4-dihydroxy-phenyl) - 3- (3-hydroxy-4-methoxy-phenyl) -propan-1-one as described in EP 2,353,403-Bl, neoisoflavonoids as described in EP 2,570,036-Bl, pellitorin and derived aroma compositions as described in EP 2 008 530 A1, vanillylignans in particular as described in the European patent application with the file reference EP 2,517,574, neoisoflavonoids as described in EP 2,570,035-Bl, neohesperidin hydrochalcone, hesperetin dihydrochalcone,
  • ingredients can be selected from the list of volatile flavorants, e.g. Acetaldehyde, acetamide, acetophenone, 2-acetylfuran, 2-acetylpyrrole, aldehyde C18 suction, benzaldehyde, benzoic acid, 2 (3H) -benzofuranone, benzonitrile, benzothiazole,
  • volatile flavorants e.g. Acetaldehyde, acetamide, acetophenone, 2-acetylfuran, 2-acetylpyrrole, aldehyde C18 suction, benzaldehyde, benzoic acid, 2 (3H) -benzofuranone, benzonitrile, benzothiazole,
  • Trimethylamine 3,5,5-trimethyl-hexanoic acid, 2,3,5-trimethylpyrazine, valeric acid, 4-vinylguajacol, 4-vinylphenol, vinylpyrazine, and mixtures of these substances.
  • compositions selected from the group comprising reaction aromas (Maillard products), extracts or essential oils of plants or plant parts or fractions thereof, smoke flavorings or other flavoring preparations (e.g.
  • Protein [part] hydrolysates, barbecue flavors, plant extracts, spices, spice preparations, vegetables and / or vegetable preparations are used.
  • flavorings or their constituents are suitable, which are not included in the mixture and a roasted, meaty (especially chicken, fish, marine animals, beef, pork, lamb, sheep, goat), vegetable (especially tomato, onion, garlic, celery , Leeks, mushrooms, eggplants, seaweed), a spicy (especially black and white pepper, chili, paprika, cardamom, nutmeg, allspice, mustard and mustard products), fried, yeasty, boiled, greasy, salty and / or pungent aroma impression cause and thus enhance the spicy impression.
  • the present invention also relates to made-up products comprising a flavoring mixture and / or a foodstuff according to the present invention. These can be food and / or supplements.
  • confectionery for example, chocolates, chocolate bar products, miscellaneous
  • alcoholic or non-alcoholic drinks for example coffee, tea, iced tea, wine, wine-based drinks, beer, beer-based drinks, liqueurs, schnapps, brandy, (carbonated) fruit-based lemonades, (carbonated ) isotonic drinks, (carbonated) soft drinks, nectars, spritzers, fruit and vegetable juices, fruit or vegetable juice preparations,
  • Instant drinks for example, instant cocoa drinks, instant tea drinks, instant coffee drinks, instant fruit drinks
  • meat products such as ham
  • Cured meat products eggs or egg products (dry egg, egg white, egg yolk), cereal products (for example breakfast cereals, muesli bars, pre-cooked finished rice products),
  • Dairy products for example, milk drinks, buttermilk drinks, milk ice cream, yogurt, kefir, cream cheese, soft cheese, hard cheese, dried milk powder, whey, whey drinks, butter, buttermilk, partially or wholly hydrolysed milk protein-containing products
  • soybean protein or other soybean meal products for example, soymilk and from it manufactured products, fruit drinks with soy protein, soy lecithin-containing preparations, fermented products such as tofu or tempe or products made from them
  • products from other vegetable protein sources for example oat protein drinks
  • Fruit preparations for example jams, fruit ice cream, fruit sauces, fruit fillings
  • vegetable preparations for example ketchup, sauces, dried vegetables, frozen vegetables, pre-cooked vegetables, cooked vegetables
  • snacks for example baked or fried potato chips or potato dough products, corn or peanut based extrudates
  • products on Fat and oil base or emulsions thereof for example, mayonnaise, remoulade, dressings
  • other prepared meals and soups for example, dry soups, instant soups, pre-cooked soups
  • the aroma mixture according to the invention can be used in particular in sports drinks, including in particular in such sports drinks that serve the regeneration of the athlete after an intense sporting activity or increase the performance.
  • a flavoring mixture is used, it is usually added in amounts of about 0.01 to 5, preferably about 0.1 to 3 and in particular about 1 to 2 wt .-%.
  • the products are food supplements, they are generally used without any further additives, although it is not possible to use any pure compounding agents.
  • the aroma preparation may be encapsulated and then also added as capsules to foods.
  • Under Capsules are spherical aggregates containing at least one solid or liquid core enclosed by at least one continuous shell.
  • Macrocapeins are preferably gelatin or spray-dried products containing polysaccharides or dextrins as a base. These usually point
  • the flavor mixture can also be encapsulated by coating materials and present as a macrocapein with diameters of about 0.1 to about 5 mm or microcapsules with diameters of about 0.0001 to about 0.1 mm.
  • microcapsule or “nanocapsule” is understood by those skilled spherical aggregates having a diameter in the range of about 0.0001 to about 5 and preferably 0.005 to 0.5 mm, containing at least one solid or liquid core, of at least enclosed in a continuous envelope. More specifically, it is coated with film-forming polymers finely dispersed liquid or solid phases, in their preparation, the polymers after emulsification and coacervation or
  • Precipitate interfacial polymerization on the material to be coated Another method involves collecting molten waxes in a matrix
  • microsponge which may be additionally enveloped as microparticles with film-forming polymers.
  • particles are coated alternately with polyelectrolytes of different charge (“layer-by-layer” method).
  • the microscopic capsules can be dried like powder.
  • mononuclear microcapsules multinuclear aggregates, also called microspheres, are known, which contain two or more cores distributed in the continuous shell material.
  • Mono- or polynuclear microcapsules can also be enclosed by an additional second, third, etc., sheath.
  • the shell may be made of natural, semi-synthetic or synthetic materials.
  • wrapping materials are gum arabic, agar-agar, agarose, maltodextrins, Alginic acid or its salts, for example sodium or calcium alginate, fats and fatty acids, cetyl alcohol, collagen, chitosan, lecithins, gelatin, albumin, shellac, polysaccharides, such as starch or dextran, polypeptides, protein hydrolysates, sucrose and waxes.
  • Semisynthetic shell materials include chemically modified celluloses, especially cellulose esters and ethers, e.g. Cellulose acetate, ethylcellulose,
  • Synthetic shell materials are, for example, polymers such as polyacrylates, polyamides, polyvinyl alcohol or
  • Suitable coating materials are, for example, starches, including their degradation products and chemically or physically generated derivatives (especially dextrins and maltodextrins), gelatin, gum arabic, agar-agar, ghatti gum, gellan gum, modified and unmodified celluloses, pullulan, curdlan, carrageenans , Alginic acid, alginates, pectin, inulin, xanthan gum and mixtures of two or more of these substances.
  • starches including their degradation products and chemically or physically generated derivatives (especially dextrins and maltodextrins), gelatin, gum arabic, agar-agar, ghatti gum, gellan gum, modified and unmodified celluloses, pullulan, curdlan, carrageenans , Alginic acid, alginates, pectin, inulin, xanthan gum and mixtures of two or more of these substances.
  • the solid encapsulating material is preferably a gelatin (especially pork, beef, poultry and / or fish gelatin), which preferably has a threshold factor of greater than or equal to 20, preferably greater than or equal to 24.
  • gelatin especially pork, beef, poultry and / or fish gelatin
  • gelatin is particularly preferred because it is readily available and with different
  • Threshold factors can be related.
  • maltodextrins especially based on cereals, especially corn, wheat, tapioca or potatoes
  • DE values in the range from 10 to 20.
  • celluloses e.g., cellulose ethers
  • alginates e.g.
  • alginate Sodium alginate
  • carrageenan eg, beta, jota, lambda and / or kappa carrageenan
  • gum arabic curdlan and / or agar agar.
  • alginate capsules as described in detail in the following documents: EP 0389700 A1, US Pat. No. 4,251,195, US Pat. No. 6,214,376, WO 2003 055587 or WO 2004 050069 A1.
  • the shell of the capsules consists of melamine-formaldehyde resins or coacervation products of cationic monomers or biopolymers (such as chitosan) and anionic monomers, such as
  • the capsules are generally finely dispersed liquid or solid phases coated with film-forming polymers, in the course of which the polymers are produced
  • Impregnate emulsification and coacervation or interfacial polymerization on the material to be coated According to another method, molten waxes are taken up in a matrix ("microsponge"), which in addition with microparticles
  • microscopically small capsules can be dried like powders
  • multinuclear aggregates also called microspheres
  • single or multinucleated microcapsules may be enclosed by an additional second, third, etc.
  • the shell may consist of natural, semisynthetic or synthetic materials, of course, shell materials include gum arabic, agar-agar , Agarose, maltodextrins, alginic acid or its salts, for example sodium or
  • Calcium alginate calcium alginate, fats and fatty acids, cetyl alcohol, collagen, chitosan, lecithins, gelatin, albumin, shellac, polysaccharides such as starch or dextran, polypeptides,
  • Semisynthetic shell materials include chemically modified celluloses, especially cellulose esters and ethers, eg Cellulose acetate, ethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose and carboxymethylcellulose, as well as starch derivatives, in particular starch ethers and esters.
  • chemically modified celluloses especially cellulose esters and ethers, eg Cellulose acetate, ethylcellulose, hydroxypropylcellulose, hydroxypropylmethylcellulose and carboxymethylcellulose, as well as starch derivatives, in particular starch ethers and esters.
  • Synthetic envelope materials are, for example, polymers such as polyacrylates, polyamides, polyvinyl alcohol or polyvinylpyrrolidone.
  • microcapsules of the prior art are the following commercial products (in parentheses is the shell material): Hallcrest Microcapsules (gelatin, gum arabic), Coletica Thalaspheres (marine collagen), Lipotec Millicapseln (alginic acid, agar-agar), Induchem Unispheres (lactose , microcrystalline cellulose, hydroxypropylmethylcellulose); Unicerin C30 (lactose, microcrystalline cellulose,
  • Hydroxypropylmethylcellulose Kobo Glycospheres (modified starch, fatty acid esters, phospholipids), Softspheres (modified agar-agar) and Kuhs Probiol Nanospheres (phospholipids), as well as Primaspheres and Primasponges (chitosan, alginates) and Primasys (phospholipids).
  • Microcapsules with average diameters in the range of 0.0001 to 5, preferably 0.001 to 0.5 and in particular 0.005 to 0.1 mm, consisting of an enveloping membrane and a matrix containing the active ingredients can be obtained, for example, by
  • step (a) and (c) are interchangeable insofar as anionic polymers are used instead of the cationic polymers in step (a) and vice versa.
  • the European patent EP 1064088 Bl Max Planck
  • Another object of the invention relates to pharmaceutical preparations for the protection of the human or animal body, comprising a novel
  • the invention further relates to cosmetic compositions containing an aroma mixture according to the invention.
  • the cosmetic compositions according to the invention may contain further typical auxiliaries and additives, for example mild surfactants, oil bodies, emulsifiers, pearlescent waxes, bodying agents, thickeners, superfatting agents, stabilizers, polymers,
  • Silicone compounds fats, waxes, lecithins, phospholipids, UV sun protection factors, humectants, biogenic agents, antioxidants, deodorants, antiperspirants, Anti-dandruff agents, film formers, swelling agents, insect repellents, self-tanner,
  • Tyrosine inhibitors (depigmentation agents), hydrotropes, solubilizers,
  • Surfactants which may be present are anionic, nonionic, cationic and / or amphoteric or zwitterionic surfactants, the proportion of which in the compositions is usually from about 1 to 70, preferably from 5 to 50, and in particular from 10 to 30,% by weight.
  • anionic surfactants are soaps, alkylbenzenesulfonates, alkanesulfonates, olefinsulfonates, alkyl ether sulfonates, glycerol ether sulfonates, ⁇ -methyl ester sulfonates, sulfo fatty acids, alkyl sulfates, alkyl ether sulfates, glycerol ether sulfates, fatty acid ether sulfates, hydroxy mixed ether sulfates, monoglyceride (ether) sulfates,
  • Alkyl oligoglucoside sulfates protein fatty acid condensates (in particular vegetable products based on wheat) and alkyl (ether) phosphates. If the anionic surfactants
  • Contain polyglycol ether these may have a conventional, but preferably a narrow homolog distribution.
  • nonionic surfactants are fatty alcohol polyglycol ethers, alkylphenol polyglycol ethers, fatty acid polyglycol esters, fatty acid amide polyglycol ethers, fatty amide polyglycol ethers, alkoxylated triglycerides, mixed ethers or optionally partially oxidized alk (en) yloligoglycosides or
  • Glucuronic acid derivatives fatty acid -N-alkylglucamides, protein hydrolysates (especially wheat-based vegetable products), polyol fatty acid esters, sugar esters, sorbitan esters, polysorbates and amine oxides.
  • nonionic surfactants are polyglycol ether chains may contain a conventional, but preferably a narrowed
  • Typical examples of cationic surfactants are quaternary ammonium compounds such as dimethyl distearyl ammonium chloride, and ester quats, especially quaternized fatty acid trialkanolamine ester salts.
  • Typical examples of amphoteric or zwitterionic surfactants are alkylbetaines, alkylamidobetaines,
  • aminopropionates aminoglycinates, imidazolinium betaines and sulfobetaines.
  • the surfactants mentioned are exclusively known compounds.
  • Typical examples of particularly suitable milds, i. particularly skin-compatible surfactants are fatty alcohol polyglycol ether sulfates, monoglyceride sulfates, mono- and / or
  • oil bodies are Guerbet alcohols based on fatty alcohols having 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-C13 carboxylic acids with linear or branched C6-C22 fatty alcohols, such as
  • esters of linear C6-C22 fatty acids with branched alcohols in particular 2-ethylhexanol
  • esters of C18-C38-alkylhydroxycarboxylic acids with linear or branched C6-C22 fatty alcohols in particular dioctyl maleate
  • esters of linear and / or branched fatty acids with polyhydric alcohols such as propylene glycol, dimerdiol or trimer triol
  • polyhydric alcohols such as propylene glycol, dimerdiol or trimer triol
  • Guerbet alcohols triglycerides based on C6-C10 fatty acids, liquid mono- / di- / Triglyceridmisonne based on C6-C18 fatty acids, esters of C6-C22 fatty alcohols and or Guerbet alcohols
  • Dicaprylyl ethers (Cetiol® OE), ring-opening products of epoxidized fatty acid esters with polyols, silicone oils (cyclomethicones, silicon methicone types and the like) and / or aliphatic or naphthenic hydrocarbons, e.g. like squalane, squalene or
  • Suitable emulsifiers are nonionic surfactants from at least one of the following groups:
  • Adducts of 1 to 15 moles of ethylene oxide with castor oil and / or hydrogenated castor oil Adducts of 1 to 15 moles of ethylene oxide with castor oil and / or hydrogenated castor oil;
  • Partial ester of polyglycerol (average intrinsic condensation degree 2 to 8),
  • Polyethylene glycol (molecular weight 400 to 5000), trimethylolpropane, pentaerythritol, sugar alcohols (eg sorbitol), alkylglucosides (eg methylglucoside, butylglucoside, laurylglucoside) and polyglucosides (eg cellulose) with saturated and / or unsaturated, linear or branched fatty acids having 12 to 22 carbon atoms and /or
  • Hydroxycarboxylic acids having 3 to 18 carbon atoms and their adducts with 1 to 30 moles of ethylene oxide;
  • Block copolymers e.g. Polyethylene glycol-30 dipolyhydroxystearates
  • Polymer emulsifiers e.g. Pemulen types (TR-1, TR-2) from Goodrich or
  • Alkoxylates (i) Alkoxylates.
  • the addition products of ethylene oxide and / or of propylene oxide onto fatty alcohols, fatty acids, alkylphenols or castor oil are known, commercially available products. These are homolog mixtures whose mean degree of alkoxylation corresponds to the ratio of the amounts of ethylene oxide and / or or
  • C12 / 18 fatty acid mono- and diesters of addition products of ethylene oxide with glycerol are known as refatting agents for cosmetic preparations.
  • alkyl and / or alkenyl oligoglycoside (ii) alkyl and / or alkenyl oligoglycoside.
  • Alkyl and / or alkenyl oligoglycosides their preparation and their use are known in the art. They are prepared in particular by reacting glucose or oligosaccharides with primary alcohols having 8 to 18 carbon atoms.
  • the glycoside radical both monoglycosides in which a cyclic sugar residue is glycosidically linked to the fatty alcohol and oligomeric glycosides having a degree of oligomerization of preferably approximately 8 are suitable.
  • the degree of oligomerization is a statistical mean, which is based on a homolog distribution typical for such technical products.
  • Isostearic acid monoglyceride isostearic acid diglyceride, oleic acid monoglyceride,
  • Erucic acid monoglyceride Erucic acid monoglyceride, erucic acid diglyceride, tartaric acid monoglyceride,
  • Sorbitan monosorbearates are sorbitan monoisostearate
  • polyglycerol esters are polyglyceryl-2 dipolyhydroxystearates (Dehymuls® PGPH), polyglycerol-3-diisostearates (Lameform® TGI), polyglyceryl-4 isostearates (Isolan® GI 34), polyglyceryl-3 oleates, diisostearoyl polyglyceryl -3 Diisostearate (Isolan® PDI), Polyglyceryl-3 Methylglucose Distearate (Tego Care® 450), Polyglyceryl-3 Beeswax (Cera Bellina®), Polyglyceryl-4 Caprate (Polyglycerol Caprate T2010 / 90), Polyglyceryl-3 Cetyl Ether (Chimexane ® NL), polyglyceryl-3 distearate (Cremophor® GS 32) and polyglyceryl polyricinoleate (Admul
  • polystyrene resin examples include the mono-, di- and triesters of trimethylolpropane or pentaerythritol with lauric acid, coconut fatty acid, tallow fatty acid, palmitic acid, stearic acid, oleic acid, behenic acid and the like, which are optionally reacted with from 1 to 30 mol of ethylene oxide.
  • Anionic emulsifiers are aliphatic fatty acids having 12 to 22 carbon atoms, such as palmitic acid, stearic acid or behenic acid, and dicarboxylic acids having 12 to 22 carbon atoms, such as azelaic acid or sebacic acid.
  • Zwitterionic surfactants are those surface-active compounds which carry 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 ⁇ , ⁇ -dimethylammoniumglycinate, for example the
  • Kokosalkyldimethylammoniumglycinat, N-acylaminopropyl-N, N-dimethylammoniumglycinate for example, the Kokosacylaminopropyldimethyl- ammoniumglycinat, and 2-alkyl-3-carboxylmethyl-3-hydroxyethylimidazoline having in each case 8 to 18 carbon atoms in the alkyl or acyl group and the
  • Kokosacylaminoethylhydroxyethylcarboxymethylglycinat Particularly preferred is the fatty acid amide derivative known under the CTFA name Cocamidopropyl Betaine.
  • emulsifiers are ampholytic surfactants. Ampholytic surfactants are understood as meaning those surface-active compounds which, apart from a C 8/18 alkyl or acyl group in the molecule, contain at least one free amino group and at least one -COOH or -SO 3 H group 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 having about 8 to 18 C - atoms in the alkyl group .
  • ampholytic surfactants are N-cocoalkylaminopropionate, cocoacylaminoethylaminopropionate and C12 / 18 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. solid or liquid vegetable or animal products consisting essentially of mixed glycerol esters of higher fatty acids, used as waxes i.a. natural waxes, e.g. Candelilla wax, carnauba wax, japan wax, esparto wax, cork wax, guaruma wax, rice germ oil wax,
  • waxes i.a. natural waxes, e.g. Candelilla wax, carnauba wax, japan wax, esparto wax, cork wax, guaruma wax, rice germ oil wax
  • Sugar cane wax ouricury wax, montan wax, beeswax, shellac wax, spermaceti, lanolin (wool wax), crepe fat, ceresin, ozokerite (earth wax), petrolatum, paraffin waxes, Microcrystalline waxes; chemically modified waxes (hard waxes), such as montan ester waxes, Sasol waxes, hydrogenated jojoba waxes and synthetic waxes, such as
  • lecithins Polyalkylene waxes and polyethylene glycol waxes in question.
  • fats come as additives and fat-like substances such as lecithins and phospholipids in question.
  • lecithin those skilled in the art will understand those glycerophospholipids which are formed from fatty acids, glycerol, phosphoric acid and choline by esterification.
  • Lecithins are therefore often referred to in the art as Phosphatidylcholine (PC).
  • PC Phosphatidylcholine
  • Examples of natural lecithins include the cephalins, which are also referred to as phosphatidic acids and derivatives of 1, 2-diacyl-sn-glycerol-3-phosphoric acids.
  • phospholipids usually mono- and preferably diesters of
  • Phosphoric acid with glycerol (glycerol phosphates), which are generally expected to be the fats.
  • glycerol phosphates glycerol phosphates
  • sphingosines or sphingolipids are also suitable.
  • Suitable pearlescing waxes are, for example: alkylene glycol esters, especially
  • ethylene glycol Fatty acid alkanolamides, especially coconut fatty acid diethanolamide;
  • Partial glycerides especially stearic acid monoglyceride
  • Fatty substances such as fatty alcohols
  • Fatty ketones, fatty aldehydes, fatty ethers and fatty carbonates which in total amount to at least 24
  • Fatty acids such as stearic acid, hydroxystearic acid or behenic acid, ring-opening products of olefin epoxides having 12 to 22 carbon atoms with fatty alcohols having 12 to 22 carbon atoms and / or polyols having 2 to 15 carbon atoms and 2 to 10 hydroxyl groups and mixtures thereof.
  • Coolants are compounds that produce a sensation of coldness on the skin.
  • these are menthol compounds which - in addition to the main body menthol itself - for example selected from the group formed by menthol methyl ether, menthone glyceryl acetal (FEMA GRAS ⁇ 1> 3807), Menthone glyceryl ketal (FEMA GRAS No.
  • menthyl lactate FEMA GRAS 3748
  • menthol ethylene glycol carbonate FEMA GRAS 3805
  • menthol propylene glycol carbonate FEMA GRAS 3806
  • menthyl-N-ethyloxamate monomethyl succinate
  • FEMA GRAS 3810 monomenthyl glutamate
  • FEMA GRAS 4006 menthoxy-1,2-propanediol
  • FEMA GRAS 3784 menthoxy-2-methyl-1,2-propanediol
  • FEMA GRAS 3849 and the menthane carboxylic acid esters and amides WS-3, WS-4, WS-5, WS-12, WS-14 and WS-30 and their mixtures.
  • FEMA Frutevor and Extracts Manufacturers Association
  • GRAS is defined as "Generally Regarded As Safe”.
  • a FEMA GRAS designation means that the substance identified in this way is tested according to the standard method and considered to be toxicologically harmless.
  • FEMA GRAS 3810 Monomenthyl succinate
  • FEMA GRAS 4006 Both the succinate and the analogous monomenthyl glutarate (FEMA GRAS 4006) are important representatives of monomenthyl esters based on di- and
  • FEMA GRAS 3805 Frescolate® MGC
  • FEMA GRAS 3849 menthol 2-methyl-1,2-propanediol carbonates
  • Menthone glyceryl acetal FEMA GRAS 3807
  • Menthone glyceryl ketal FEMA GRAS 3808
  • Frescolat® MGA Menthone glycerol acetal / ketal and the menthyl lactate and menthol ethylene glycol carbonates or menthol propylene glycol carbonate w, which the applicant has designated Frescolat ⁇ ®> MGA, Frescolat ⁇ ®> ML, Frecolat ⁇ ®> MGC and Frescolat ⁇ ®> MPC sells.
  • menthol compounds were developed for the first time, which have a C-C bond in the 3-position and from which a number of representatives can also be used. These substances are generally referred to as WS types.
  • Base is a menthol derivative in which the hydroxyl is replaced by a carboxyl group (WS-1). From this structure, all other types of WS are derived, such as the preferred species WS-3, WS-4, WS-5, WS-12, WS-14 and WS-30.
  • Fatty acids or hydroxy fatty acids into consideration. Preference is given to a combination of these substances with alkyl oligoglucosides and / or fatty acid N-methylglucamides of the same chain length and / or polyglycerol poly-12-hydroxystearates.
  • Suitable thickening agents 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, sepiolite types from Seppic, Salcare types from Allied Colloids), polyacrylamides, polymers, polyvinyl alcohol and Polyvinylpyrrolidone. Be particularly effective bentonites, such as
  • Cyclopentasiloxane, disteardimonium hectorite and propylene carbonate are also suitable.
  • surfactants such as, for example, ethoxylated fatty acid glycerides, esters of fatty acids with polyols, for example pentaerythritol or trimethylolpropane, fatty alcohol ethoxylates with narrow homolog distribution or alkyl oligoglucosides and also electrolytes, such as common salt and ammonium chloride.
  • Superfatting agents may be substances such as lanolin and lecithin, as well as polyethoxylated or acylated lanolin and lecithin derivatives, polyol fatty acid esters,
  • Monoglycerides and fatty acid alkanolamides are used, the latter also serve as foam stabilizers.
  • metal salts of fatty acids e.g. Magnesium, aluminum and / or zinc stearate or ricinoleate can be used.
  • Suitable cationic polymers are, for example, cationic cellulose derivatives, e.g. a quaternized hydroxyethylcellulose available under the name Polymer JR 400® from Amerchol, cationic starch, copolymers of diallylammonium salts and acrylamides, quaternized vinylpyrrolidone / vinylimidazole polymers, e.g. Luviquat® (BASF), condensation products of polyglycols and amines, quaternized
  • cationic cellulose derivatives e.g. a quaternized hydroxyethylcellulose available under the name Polymer JR 400® from Amerchol, cationic starch, copolymers of diallylammonium salts and acrylamides, quaternized vinylpyrrolidone / vinylimidazole polymers, 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, polyethylenimine, cationic silicone polymers such as amodimethicones, copolymers of adipic acid and dimethylaminohydroxypropyldiethylenetriamine (Cartaretine® / Sandoz), copolymers of Acrylic acid with dimethyl diallyl ammonium chloride (Merquat® 550 / Chemviron), polyaminopolyamides and their crosslinked water-soluble polymers, cationic
  • Chitin derivatives such as quaternized chitosan, optionally microcrystalline distributed, condensation products of 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 come in the art.
  • vinyl acetate / crotonic acid copolymers for example, vinyl acetate / crotonic acid copolymers, vinylpyrrolidone / vinyl acrylate copolymers, vinyl acetate / butyl maleate / isobornyl acrylate copolymers,
  • 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
  • Room temperature may be both liquid and resinous. Also suitable are simethicones, which are mixtures of Dimethicone with a
  • UV sun protection factors average chain length of from 200 to 300 dimethylsiloxane units and hydrogenated silicates. 11. UV sun protection factors
  • UV sunscreen factors for example, at room temperature, liquid or crystalline organic substances (sunscreen) to understand that are able to absorb ultraviolet rays and the absorbed energy in the form of longer-wave radiation, e.g. Heat again.
  • the UV sunscreen factors are present in amounts of 0.1 to 5 and preferably 0.2 to 1 wt .-%.
  • UVB filters can be oil-soluble or water-soluble. As oil-soluble substances are e.g. to call:
  • 4-aminobenzoic acid derivatives preferably 2-ethylhexyl 4- (dimethylamino) benzoate, 2-octyl 4- (dimethylamino) benzoate and 4- (dimethylamino) benzoic acid ester;
  • Esters of cinnamic acid preferably 4-methoxycinnamic acid 2-ethylhexyl ester, 4-methoxycinnamic acid propyl ester, 4-methoxycinnamic acid isoamyl ester 2-cyano-3,3-phenylcinnamic acid 2-ethylhexyl ester (octocrylene);
  • Esters of salicylic acid preferably 2-ethylhexyl salicylate, 4-isopropylbenzyl salicylate, homomenthyl salicylate;
  • benzophenone preferably 2-hydroxy-4-methoxybenzophenone, 2-hydroxy-4-methoxy-4'-methylbenzophenone, 2,2'-dihydroxy-4-methoxybenzophenone;
  • Esters of benzalmalonic acid preferably di-2-ethylhexyl 4-methoxybenzmalonate
  • Triazine derivatives e.g. 2,4,6-trianilino (p-carbo-2'-ethyl-hexyloxy) -l, 3,5-triazine and octyl triazone or dioctyl butamido triazone (Uvasorb® HEB);
  • Propane-1,3-diones e.g. l- (4-tert-butylphenyl) -3- (4'methoxyphenyl) propane-l, 3-dione;
  • Suitable water-soluble substances are: 2-phenylbenzimidazole-5-sulfonic acid and its alkali, alkaline earth, ammonium,
  • Sulfonic acid derivatives of benzophenones preferably 2-hydroxy-4-methoxybenzophenone-5-sulfonic acid and its salts;
  • Sulfonic acid derivatives of the 3-benzylidene camphor e.g. 4- (2-Oxo-3-bornylidenemethyl) benzenesulfonic acid and 2-methyl-5- (2-oxo-3-bomylidene) -sulfonic acid and its salts.
  • UV-A filter in particular derivatives of benzoylmethane are suitable, such as, for example, 1- (4'-tert-butylphenyl) -3- (4'-methoxyphenyl) propan-1, 3-dione, 4-tert-butyl 4'-methoxydibenzoylmethane (Parsol® 1789), 2- (4-diethylamino-2-hydroxybenzoyl) benzoic acid hexyl ester (Uvinul® A Plus), 1-phenyl-3- (4'-isopropylphenyl) -propane-1, 3-dione and enamine compounds.
  • the UV-A and UV-B filters can also be used in
  • benzoylmethane e.g. 4-tert-butyl-4'-methoxydibenzoylmethane (Parsol® 1789) and 2-cyano-3,3-phenylcinnamic acid 2-ethylhexyl ester (octocrylene) in combination with esters of cinnamic acid, preferably 2-ethylhexyl 4-methoxycinnamate and / or 4-methoxycinnamic acid propyl ester and / or 4-methoxycinnamic acid isoamyl ester.
  • water-soluble filters e.g. 2-phenylbenzimidazole-5-sulfonic acid and its alkali, alkaline earth, ammonium, alkylammonium,
  • Light protection pigments namely finely dispersed metal oxides or salts in question.
  • suitable metal oxides are in particular zinc oxide and titanium dioxide and, in addition, oxides of iron, zirconium, silicon, manganese, aluminum and cerium and mixtures thereof.
  • salts silicates (talc), barium sulfate or zinc stearate can be used.
  • the oxides and Salts are used in the form of the pigments for skin-care and skin-protecting emulsions and decorative cosmetics.
  • the particles should have an average diameter of less than 100 nm, preferably between 5 and 50 nm and in particular between 15 and 30 nm.
  • the pigments may have a spherical shape, but it is also possible to use those particles which have an ellipsoidal or otherwise deviating shape from the spherical shape.
  • the pigments can also be surface-treated, ie hydrophilized or hydrophobized.
  • Typical examples are coated titanium dioxides, such as titanium dioxide T 805 (Degussa) or Eusolex ⁇ ®> T2000, Eusolex ⁇ ®> T,
  • Suitable hydrophobic coating agents are in particular silicones and in particular trialkoxyoctylsilanes or simethicones.
  • sunscreens so-called micro- or nanopigments are preferably used.
  • micronized zinc oxide e.g. Z-COTE ⁇ ®> or Z-COTE HPl ⁇ ®>. 12.
  • Humectants serve to further optimize the sensory properties of the composition and to regulate the moisture of the skin. At the same time, the low-temperature stability of the preparations according to the invention, in particular in the case of emulsions, is increased.
  • the humectants are usually contained in an amount of 0.1 to 15 wt .-%, preferably 1 to 10 wt .-%, and especially 5 to 10 wt .-%.
  • Suitable according to the invention are i.a. Amino acids, pyrrolidonecarboxylic acid, lactic acid and its salts, lactitol, urea and urea derivatives, uric acid, glucosamine,
  • Creatinine cleavage products of collagen, chitosan or chitosan salts / derivatives, and in particular polyols and polyol derivatives (eg glycerol, diglycerol, triglycerol,
  • humectants are glycerol, diglycerol, triglycerol and butylene glycol.
  • biogenic active substances examples include tocopherol, tocopherol acetate,
  • Fragmentation products ⁇ -glucans, retinol, bisabolol, allantoin, phytantriol, panthenol, AHA acids, amino acids, ceramides, pseudoceramides, essential oils, plant extracts, e.g. Prunus extract, Bambaranussex Relax and vitamin complexes to understand.
  • Antioxidants interrupt the photochemical reaction chain, which is triggered when UV radiation penetrates the skin.
  • Typical examples are amino acids (eg glycine, histidine, tyrosine, tryptophan) and their derivatives, imidazoles (eg urocaninic acid) and their derivatives, peptides such as D, L-carnosine, D-carnosine, L-carnosine and their derivatives (eg anserine) , Carotenoids, carotenes (eg ⁇ -carotene, ⁇ -carotene, lycopene) and their derivatives, chlorogenic acid and its derivatives, lipoic acid and derivatives thereof (eg dihydrolipoic acid), aurothioglucose, propylthiouracil and other thiols (eg thioredoxin, glutathione, cysteine, cystine, Cystamine and its glycosyl, N-acetyl, methyl, ethyl, propyl, amyl, butyl and lauryl, palmitoyl, o
  • Sulfoximine compounds e.g., buthionine sulfoximines, homocysteinesulfoximine,
  • Butioninsulfone, penta-, hexa-, heptathionine sulfoximine) in very low tolerated dosages eg pmol to ⁇ / kg
  • metal chelators eg a-hydroxy fatty acids, palmitic acid, phytic acid, lactoferrin
  • ⁇ -hydroxy acids eg citric acid, lactic acid, Malic acid
  • humic acid eg bile acid, bile extracts, bilirubin, biliverdin, EDTA, EGTA and their derivatives
  • unsaturated fatty acids and their derivatives eg ⁇ -linolenic acid, linoleic acid, oleic acid
  • folic acid and its derivatives ubiquinone and ubiquinol and derivatives thereof, vitamin C and derivatives (eg ascorbyl palmitate, Mg ascorbyl phosphate,
  • hydrotropes such as, for example, ethanol, isopropyl alcohol, or polyols; These substances largely correspond to the initially described carriers.
  • Polyols contemplated herein preferably have from 2 to 15 carbon atoms and at least two hydroxyl groups.
  • the polyols may contain other 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
  • Trimethylolbutane pentaerythritol and dipentaerythritol
  • Lower alkyl glucosides especially those having 1 to 8 carbons in the alkyl radical, such as, for example, methyl and butyl glucoside;
  • Sugar alcohols with 5 to 12 carbon atoms such as sorbitol or mannitol,
  • sugars having 5 to 12 carbon atoms such as glucose or sucrose
  • Dialcoholamines such as diethanolamine or 2-amino-l, 3-propanediol. 15. Preservative
  • Suitable preservatives are, for example, phenoxyethanol, formaldehyde solution, parabens, pentanediol or sorbic acid and those under the name
  • Natural fragrances are extracts of flowers (lily, lavender, roses, jasmine, neroli, ylang-ylang), stems and leaves (geranium, patchouli, petitgrain), fruits (aniseed, coriander, caraway, juniper), fruit peel (bergamot, lemon, Oranges), roots (macis, 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, pines), resins and balsams (galbanum, elemi, benzoin, myrrh, olibanum, opoponax).
  • Typical synthetic fragrance compounds are ester type products, ethers, aldehydes, ketones, alcohols and hydrocarbons. Fragrance compounds of the ester type are, for example Benzyl acetate, phenoxyethyl isobutyrate, p-tert-butylcyclohexyl acetate, linalyl acetate,
  • Benzyl salicylate include, for example, benzyl ethyl ether, to the aldehydes e.g. the linear alkanals with 8 to 18 carbon atoms, citral, citronellal,
  • the hydrocarbons mainly include the terpenes and balsams.
  • mixtures of different fragrances are used, which together produce an attractive fragrance.
  • lower volatility volatile oils which are most commonly used as aroma components, are useful as perfume oils, e.g. Sage oil,
  • Juniper berry oil Juniper berry oil, vetiver oil, oliban oil, galbanum oil, labolanum oil and lavandin oil.
  • bergamot oil dihydromyrcenol, lilial, lyral, citronellol,
  • Suitable flavors are, for example, peppermint oil, spearmint oil, aniseed oil, star aniseed oil, caraway oil, eucalyptus oil, fennel oil, citron oil, wintergreen oil, clove oil, menthol and the like.
  • Dyes the substances suitable and suitable for cosmetic purposes can be used, as compiled, for example, in the publication "Cosmetic Colorants” of the Dye Commission of the Irish Klastician, Verlag Chemie, Weinheim, 1984, pp. 81-106. Examples are Kochillerot A (CI 16255),
  • Patent Blue V (C.I.42051), indigotine (C.I.73015), chlorophyllin (C.I.75810), quinoline yellow (C.I.47005), titanium dioxide (C.I.77891), indanthrene blue RS (C.I. 69800) and cracker paint
  • luminescent dye and luminol may be included. These dyes are usually used in concentrations of 0.001 to 0.1 wt .-%, based on the total mixture.
  • the total amount of auxiliaries and additives may be 1 to 50, preferably 5 to 40 wt .-% - based on the means - amount.
  • the preparation of the agent can be carried out by conventional cold or hot processes; It is preferable to work according to the phase inversion temperature method.
  • Example 1 Reduction of the unpleasant notes in soy sauce containing biogenic amines
  • the panellists receive the product alone in one sample, and in another sample the product that has been treated with an amount of substances listed in the table. The order is arbitrary and not previously known to the panellists.
  • the following table summarizes the results of the tests.
  • Example 2 Reduction of unpleasant fish sauce scores - Triangel Test
  • Commercially available fish sauces are used for the experiments and selected from those containing 8 ppm phenylethylamine, 99 ppm histamine, 121 ppm cadaverine and 61 ppm putrescine by analysis and by panelists to the others
  • the pannelists received the following instructions: Please scratch the three samples and tick the different samples. In any case, one of the samples must be ticked, even if no difference can be detected.
  • Example 3 Use of a flavoring mixture containing both components
  • two aroma mixtures A and B which have the following composition:
  • Triglyceride vegetable oil 98.8% by weight
  • Flavor mixture B ⁇ -damascenone 0.2% by weight
  • Triglyceride vegetable oil 98.4% by weight
  • Beer B 0,025 maltier sweeter compared to 4 sour, spicy, fruity, carbonated

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Abstract

L'invention concerne un mélange aromatique destiné à la réduction de l'odeur ou du goût d'amines biogènes. La présente invention concerne un mélange aromatique ou une denrée alimentaire comprenant de l'ionone ou un composé voisin ainsi qu'une 1,4 pyrazine alkylée. Ainsi le goût et l'odeur désagréables des amines biogènes sont réduits.
EP16822452.5A 2016-12-20 2016-12-20 Mélange aromatique destiné à la réduction de l'odeur ou du goût d'amines biogènes Pending EP3558030A1 (fr)

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PCT/EP2016/081939 WO2018113925A1 (fr) 2016-12-20 2016-12-20 Mélange aromatique destiné à la réduction de l'odeur ou du goût d'amines biogènes

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EP3558030A1 true EP3558030A1 (fr) 2019-10-30

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US (1) US20210127719A1 (fr)
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WO (1) WO2018113925A1 (fr)

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CN115334906A (zh) * 2020-03-26 2022-11-11 味之素株式会社 掩蔽剂
WO2023186333A1 (fr) 2022-03-30 2023-10-05 Symrise Ag Rouleau de papier faisant office de système de commande de diffusion de parfum

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US5250512A (en) * 1990-05-17 1993-10-05 Takasago International Corporation Propanol derivatives and perfumes containing the same
EP0941671B1 (fr) * 1998-03-12 2015-09-09 International Flavors & Fragrances Inc. Agent de goût provenant du Saccharum Officinarum, procédé pour le préparer, produits le comprenant
JP5290721B2 (ja) * 2008-12-08 2013-09-18 株式会社ミツカングループ本社 鰹節抽出物または鰹節抽出物入り調味料の風味向上方法
GB0906009D0 (en) * 2009-04-07 2009-05-20 Givaudan Sa Organic compounds
JP5989301B2 (ja) * 2011-01-12 2016-09-07 キッコーマン株式会社 調味料
JP5826108B2 (ja) * 2012-05-11 2015-12-02 株式会社ファンケル 加水分解コラーゲン含有粉末
CN104684413A (zh) * 2012-10-02 2015-06-03 高砂香料工业株式会社 虾味组合物和虾风味增强剂

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US20210127719A1 (en) 2021-05-06

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