WO2018095533A1

WO2018095533A1 - Mixtures with stabilising properties

Info

Publication number: WO2018095533A1
Application number: PCT/EP2016/078808
Authority: WO
Inventors: Melanie Stürtz; Gerhard Krammer; Günter Kindel; Birgit Kohlenberg; Marcus Eggers; Nicole Schulze; Julie SICART; Renske TIJSSEN; Alessia ERMACORA
Original assignee: Symrise AG
Current assignee: Symrise AG
Priority date: 2016-11-25
Filing date: 2016-11-25
Publication date: 2018-05-31
Anticipated expiration: 2019-05-25
Also published as: MX374474B; WO2018096123A1; US20190336423A1; EP3397072B1; MX2019005755A; EP3397072A1; US11219230B2

Abstract

The present invention primarily relates to novel mixtures with stabilizing properties, particularly for avoiding, reducing or delaying the formation of sensorially undesired flavours and/or tastes in oxidative degradation processes or autoxidative processes or reducing, avoiding or delaying oxidative processes in one or more oxidation-sensitve compounds, particularly autoxidative processes, their use in specific preparations as well as novel preparations and methods of producing such preparations. Additionally, herein described are methods for decreasing, avoiding or delaying the formation of sensorially undesired flavours and/or tastes in oxidative degradation processes or autoxidative processes or for decreasing, avoiding or delaying oxidative processes in one or more oxidation-sensitive compounds, particularly autoxidative processes.

Description

Mixtures with stabilising properties

The present invention primarily relates to novel mixtures with stabilising properties, particularly for reducing, delaying or avoiding the formation of sensorially undesired degradation products/ compounds of oxidative processes (particularly for reducing, delaying or avoiding the formation of sensorially undesired flavours and/or tastes), particularly with oxidation-slowing or oxidation-inhibiting effect, their use in certain preparations, as well as novel preparations and methods of producing such preparations. The present invention further relates to methods for decreasing, avoiding or delaying the formation of sensorially undesired degradation products/ compounds of oxidative processes (particularly for reducing, delaying or avoiding the formation of sensorially undesired flavours and/or tastes), particularly of autoxidative processes.

Further aspects of the present invention and preferred embodiments will arise from the following description and the enclosed patent claims. Oxidative degradation processes and autoxidative processes play an important role for the sensorial stability of preparations, since they can destroy desired ingredients that then are no longer present or else undesired degradation products form that can produce unpleasant or undesired sensorial impressions. Ingredients that are often affected by this are, for example, flavouring substances that are of importance for the sensorial properties and the flavour, respectively, of a preparation and whose degradation and absence, respectively, usually negatively affects the overall sensorial impression of the preparation. The formation of the sensorially undesired degradation substances or compounds can be forced by the influence of warmth, that may occur, for example, during processing steps or during storage or transport as well as by the influence of light and UV irradiation, metal cations, air or certain enzymes, respectively. Further ingredients affected thereby are, for example, fats, oils, fatty acids, fatty acid esters and fatty acid derivatives, respectively, that are attacked and transformed or destroyed, respectively, by oxidative degradation processes and autoxidative processes. Substances that can produce an undesired flavour and/or an undesired taste in the preparation often are formed thereby. The sensorial properties and the flavor of a preparation, respectively, represent considerable quality features that may be the deciding factor for the purchase as well as the market.

The oxidative degradation of certain ingredients therefore often decreases the value of the product. This does not only affect food, but also, for example, cosmetics and pharmaceuticals. With these preparations it is particularly disadvantageous when unpleasant degradation products form and/or physical performance characteristics decrease because of oxidative degradation of the ingredients.

Document WO2013/189709A1 relates to a method of production of an EDTA-free mayonnaise by means of using a combination of reduced grape juice, acetic acid and proteins, whereby tartaric acid and malic acid as well as glucose and fructose are disclosed as components of the reduced grape juice. This described combination serves as EDTA-substitute and has oxidation-stabilising properties.

The article "Model Studies on the Antioxidant Activity of common Terpenoid Constituents of Essential Oils by Means of the 2,2-Diphenyl-1-picrylhydrazyl Method" by K.A. Woijtunik, L.M. Ciesla and M. Waksmundzka-Hajnos in the Journal of Agriculture and Food Chemistry (2014, 62, 9088-9094) discloses monoterpenes as antioxidants, particularly pulegone, citral, gamma-terpinene, myrcene and alpha-phellandrene.

Common methods for counteracting oxidative degradation processes and autoxidative processes therefore are often based on the use of EDTA or antioxidants. Since the use of EDTA is regulated and only possible conditionally, there is an ongoing strong interest in alternative solutions to decrease or to avoid the oxidative degradation processes and autoxidative processes, respectively, and thereby the formation of substances causing undesired flavours and/or tastes and/or other disadvantageous effects (cf. above).

It was therefore the primary task of the invention to provide novel agents, particularly novel oxidation-slowing or oxidation-inhibiting or anti-autoxidative agents, with stabilizing properties that are suitable to decrease or to avoid undesired flavours and/or tastes that are formed or have formed during oxidative degradation processes and autoxidative processes or to slow down their formation and/or to retain the desired flavours and/or tastes and thereby to improve or to stabilize the sensorial durability and to overall improve the quality of flavoured preparations, respectively. Such agents preferably should be widely applicable so that they are not restricted to the use in specific preparations. Further details of this primary purpose, further problems underlying the present invention and individual or preferred aspects thereof will arise from the present description, the example section as well as particularly from the enclosed patent claims.

Within the scope of the present text, a stabilising property is preferably understood to be the property to slow down or to avoid altogether the change of substances during storage or processing or production of ingredients, in particular of ingredients and constituents of food and flavouring substances or to retain the formation of desired compounds.

Within the scope of the present text, an anti-autoxidative effect is preferably understood to be the property of chemical compounds or mixtures to slow down or to avoid altogether oxidative degradation processes and autoxidative processes of other substances, respectively.

The primary task of the present invention is solved by a mixture comprising or consisting of a) one or more monocyclic monoterpenes of formula (I)

(I) with R1 = hydrogen, hydroxy group or carbonyl group, R2 = hydrogen, hydroxy group or carbonyl group, R3 = 0 (according to one alternative, R3 is not present), hydrogen or hydroxy group and R4 = isopropyl group, isopropenyl group or isopropylidene group as well as without or with one, two or three double bonds in the cyclic system, preferably selected from the group consisting of gamma-terpinene, alpha- terpinene, beta-terpinene, beta-phellandrene, limonene, thymol, pulegone, carvacrol and alpha-phellandrene, one or more benzoic acid derivatives of formula (II)

(II) with R1 , R2 and R3 independently of each other selected from the group consisting of hydrogen, hydroxy group and methoxy group, a first 3-phenylpropenoic acid derivative of formula (IV)

(IV) with R1 = 1-carboxy-2-(3,4-dihydroxyphenyl)ethyl, R2 = hydrogen and R3 = hydrogen, optionally a second 3-phenylpropenoic acid derivative of formula (IV) with R1 = 5-carboxy-2,3,5-trihydroxycyclohexyl, R2 = hydrogen and R3 = hydrogen, and

optionally a third 3-phenylpropenoic acid derivative of formula (IV) with R1 = hydrogen, R2 = hydrogen and R3 = hydrogen, or, respectively,

3-(3,4-dihydroxyphenyl)-2-[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy- propionic acid, optionally 3-[3-(3,4-dihydroxyphenyl)prop-2-enoyl]oxy-1 ,4,5-trihydroxy- cyclohexane-1-carboxylic acid, and optionally 3-(3,4-dihydroxyphenyl)prop-2-enoic acid, d) tartaric acid (formula (V))

D-(-)-form, and/or L-(+)-form, and/or meso-form

(V), e) citric acid (formula (VI)) and/or malic acid (formula (VII))

f) glucose, fructose and/or sucrose, g) 1 ,2-propanediol and/or 1 ,3-propanediol and/or propane-1 ,2,3-triol, h) water, i) optionally gallocatechin (Formula (III))

(2R,3S)-3,4-dihydro-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-3,5,7-triol

(Hi), j) optionally one or more further flavouring substances, and k) optionally one or more further solvents, preferably selected from the group consisting of triacetin (TRI), isopropanol (iPr), isopropyl myristate (IPM), ethanol, dipropylene glycol (DPG) and triethyl citrate (TEC).

Such mixtures demonstrate particularly advantageous stabilizing properties and oxidation-decelerating, oxidation-inhibiting or anti-autoxidative effects, respectively, according to the studies carried out within the scope of the present invention. The mixtures according to the invention are particularly well suited to reduce or to avoid altogether undesired flavours and/or tastes that are formed or have formed by oxidative degradation and autoxidation, respectively, or to slow down their formation. Thereby, advantageously a better sensorial durability and stabilization of the preparation containing such substances can be achieved. Additionally, the mixtures according to the invention are thereby widely applicable, particularly as component of specific preparations containing one or more oxidation-sensitive compounds (as described herein). The individual substances of the mixture according to the invention are not able to slow down or to avoid altogether the formation of undesired flavours and/or tastes by oxidative degradation and autoxidation, respectively, over a longer period to the same extent as mixtures according to the invention are able to, so that less undesired degradation products are formed, that can produce unpleasant or undesired sensorial impressions. Within the scope of the present invention it is preferred that the mixture according to the invention has an ORAC value of greater than 200 μιηοΙ TE/g, with respect to the dry weight of the mixture, preferably of greater than 500 μιηοΙ TE/g, particularly preferably of greater than 1000 μιηοΙ TE/g, especially preferably of greater than 2000 μιηοΙ TE/g. ORAC stands for Oxygen Radical Absorption Capacity. The ORAC value determines the antioxidative ability or capacity of a substance or a mixture and is given in ORAC units (μητιοΙ TE/g) within the scope of the present text. The ORAC value therefore represents a characteristic measure of the antioxidative potential as is described in more detail in document WO20141471 12 (A1 ). According to a further preferred embodiment of the present invention the mixture has a polyphenol content according to Folin-Ciocalteu of greater than 5 %, with respect to the dry weight of the mixture, preferably of greater than 10 %, particularly preferably of greater than 15 %.

The determination of the ORAC value and of the polyphenol content according to Folin- Ciocalteu took place during studies within the scope of the present invention and therefore also takes place within the scope of the present text generally following "Standardized Methods for the Determination of Antioxidant Capacity and Phenolics in Food and Dietary Supplements" by R.L. Prior, X. Wu and K. Schaich, Journal of Agriculture and Food Chemistry, 2005, 53, 4290-4302. Because of their stabilising properties and oxidation-decelerating or oxidation-inhibiting or anti-autoxidative effects, respectively, the mixtures according to the invention are particularly well suited to reduce or to avoid undesired flavours and/or tastes (also known as off-tastes, off-flavours, off-notes, off-odours, bad scents, malodor, taste defects) that occur within the scope of oxidative and autoxidative processes or to slow down their formation. Such undesired off-notes are often described with terms such as, for example, rancid, roasty, nutty, bitter, pungent, poignant, scratchy, hay-like, chemical, technical, burnt, fatty, sour, herbaceous, stale, foul, fermented, aromatic, meaty, green, charred, fungal, smoky, buttery, vegetable-like, cooked, cheesy, carbonaceous, hot, fruity, metallic, dusty, spicy, powdery, sticky, floury or dry. Preferred formulations of mixtures according to the invention comprise or consist of, respectively, components a) to h) as well as optionally i) to k) in the following amounts with regard to the total weight of the mixture, respectively: 0.0001 to 80 wt.-% of component a), preferably 0.001 to 10 wt.-%, particularly preferably 0.01 to 5 wt.-%, especially preferably 0.1 to 1 wt.-%,

0.0001 to 1.5 wt.-% of component b), preferably 0.001 to 1 wt.-%, particularly preferably 0.005 to 0.25 wt.-%, especially preferably 0.01 to 0.1 wt.-%

0.0001 to 3 wt.-% of component c), preferably 0.001 to 1.5 wt.-%, particularly preferably 0.005 to 1 wt.-%, especially preferably 0.01 to 0.7 wt.-%

0.005 to 10 wt.-% of component d), preferably 0.0075 to 5 wt.-%, particularly preferably 0.01 to 3 wt.-%, especially preferably 0.01 to 0.5 wt.-%

0.005 to 10 wt.-% of component e), preferably 0.0075 to 8 wt.-%, particularly preferably 0.01 to 5 wt.-%, especially preferably 0.01 to 3 wt.-%

0.000005 to 25 wt.-% of component f), preferably 0.0000075 to 15 wt.-%, particularly preferably 0.00001 to 10 wt.-%, especially preferably 0.00005 to 5 wt.-

%

0.0001 to 98 wt.-% of component g), preferably 0.0005 to 65 wt.-%, particularly preferably 0.001 to 45 wt.-%, especially preferably 0.1 to 35 wt.-%

0.0005 to 95 wt.-% of component h), preferably 0.005 to 65 wt.-%, particularly preferably 0.01 to 50 wt.-%, especially preferably 0.05 to 35 wt.-%

0.0001 to 1 wt.-% of component i), preferably 0.001 to 0.7 wt.-%, particularly preferably 0.005 to 0.5 wt.-%, especially preferably 0.01 to 0.15 wt.-%

0.005 to 95 wt.-% of component j), preferably 0.0075 to 50 wt.-%, particularly preferably 0.01 to 25 wt.-%, especially preferably 0.05 to 15 wt.-%

0.01 to 95 wt.-% of component k), preferably 0.05 to 65 wt.-%, particularly preferably 0.1 to 45 wt.-%, especially preferably 1 to 35 wt.-%.

Thereby, within the scope of the present invention, it applies that also such mixtures are preferred according to the present invention that do not fulfill all of the above-named wt.- % ranges, i.e. that comprise one or more of the components a) to h) as well as optionally i), j) and k) within the range of the above-named wt.-% ranges, but apart from that differ from the above-named ranges. However, in principle it applies that mixtures that correspond to the above-named formulation are particularly preferred.

According to a preferred embodiment of a mixture according to the invention, the mixture is a flavor composition. Such mixture then regularly comprises the above-named component j), i.e. one or more further flavouring substances.

Flavouring substances in terms of the present invention preferably are substances that are defined by e.g. regulation (EG) No. 2232/96 of the European Parliament and Council and the positive list according to the implementing provision (EU) No. 872/2012 of the Commission, and the substances that are listed in "Riechstoffe" by Steffen Arctander, in „Perfume and Flavor Chemicals" published on his own, Montclair, N. J. 1969 as well as in „Common Fragrance and Flavor Materials" by H. Surburg, J. Panten, 5th Edition, Wiley- VCH, Weinheim 2006.

Examples for flavouring substances in terms of the present invention are - saturated or unsaturated esters such as for example ethyl butyrate, benzyl acetate, methyl salicylate, neryl acetate, geranyl acetate, allyl capronate, anisyl acetate, anisyl formiate, butyl butyrate, butyl capronate, butyliden phthalide, cinnamyl acetate, benzyl benzoate, citronellyl acetate, cyclohexyl acetate, dimethyl anthranilate, ethoxyethyl acetate, ethyl butyrate, ethyl caprinate, ethyl capronate, ethyl crotonate, ethyl isobutyrate, ethyl isovalerianate, ethyl lactate, ethylmethyl butyrate, ethyl propionate, ethyl heptylate, methyldihydro jasmonate (e.g. Hedion®), cis-2-hexenyl acetate, cis-3-hexenyl acetate, cis-3-hexenyl capronate, trans-2-hexenyl capronate, cis-3-hexenyl formiate, cis-2-hexyl acetate, cis-3-hexyl acetate, trans-2-hexyl acetate, cis-3-hexyl formiate, isoamyl isovalerianate, isobutyl butyrate, linalyl acetate, methyl anthranilate, 2-methylbutyl acetate, methyl capronate, methyl cinnamate, methyl jasmonate, 2-methyl methylbutyrate, methylthio butyrate, 3-methylthio hexyl acetate, neryl acetate, 1-octyl acetate, 3-octyl acetate, phenylethyl acetate, phenylethyl isovalerianate, propyl butyrate, ethyl vanillin isobutyrate, acetic acid isoamyl ester, butyric acid ethyl ester, butyric acid n- butyl ester, butyrid acid isoamyl ester, 3-methyl-butyric acid ethyl ester, n-hexanoic acid ethyl ester, n-hexanoic acid allyl ester, n-hexanoic acid n-butyl ester, n-octanoic acid ethyl ester, ethyl-3-methyl-3-phenylglycidate, ethyl-2-trans-4-cis-decadienoate, methyl salicylate, methyl sorbate; saturated or unsaturated organic acids such as for example butyric acid, acetic acid, methylbutyric acid, caproic acid, ethylbutyric acid, trans-2-hexenoic acid, trans-3- hexenoic acid, lauric acid, levulinic acid, 2-methyl-2-pentenoic acid, palmitic acid, valeric acid; - saturated or unsaturated alcohols such as for example octenol, cis-3-hexanol, benzyl alcohol, phenylethyl alcohol, eugenol, cis-3-hexenol, isoamyl alcohol, methyl butanol, 3, 1-methylthio-hexanol, 2,4-nonadienol, 2,6-nonadienol, 2,4-nonadienol, 2- octanol, 3-octanol, 1 ,3-octenol, phenylethyl alcohol, cinnamyl alcohol; saturated or unsaturated aldehydes such as for example acetaldehyde, isobutyric aldehyde, nonadienal, 3-phenylacetaldehyde, anisaldehyde, benzaldehyde, grapefruit aldehyde, heliotropin, trans-2-heptenal, cis-4-heptenal, trans-2-hexenal, 5-methylfurfural, trans,trans-2,4-Nonadienal, paraldehyde, piperonal, propionaldehyde, vanillin, ethylvanillin, acetoin, divanillin, phenylacetaldehyde, methional, (E,E)-2,4-decadienal, (E,E)-2,4-nonadienal, (E)-2-octenal, (E)-2-nonenal, 2-undecenal, 12-methyl tridecanal, cinnamic aldehyde; ketones such as for example menthon, acetophenone, alpha-ionone, beta-ionone, damascone, 4-(p-hydroxyphenyl)-2-butanone, 2-heptanone, 3-heptanone, 4-heptanone, para-hydroxybenzyl acetone, 3,2,2-methyl cyclopentenolone, 6,5,2-methyl heptenone, nootkatone, pentandione, 4-(p-hydroxyphenyl)-2-butanone; - ethers such as for example 4-hydroxy-5-m ethyl furanone, 3-hydroxy-4,5-dimethyl- 2-(5H)-furanone, 2,5-dimethyl-3-hydroxy-2(3H)-furanone, 2(5)-ethyl-4-hydroxy-5(2)- methyl-3(2H)-furanone, p-methoxybenzaldehyde, guajacol, methoxyvinyl phenol, ethyl furaneol, ethylguajacol, isoeugenol methyl ether, menthofuran, 2,5-dimethyl-4-hydroxy- 3(2H)-furanond, homofuraneol (= 2-ethyl-4-hydroxy-5-methyl-3(2H)-furanone), homofuronol (= 2-ethyl-5-methyl-4-hydroxy-3(2H)-furanone and 5-ethyl-2-methyl-4- hydroxy-3(2H)-furanone, 1 , 1-dimethoxy-2,2,5-trimethyl-4-hexane; acetals such as for example acetaldehyde diethyl acetal; lactones such as for example gamma-decalactone, dihydrocumarin, dodecalactone, nonalactone, methyl delta decalactone, massoia lactone, delta decalactone, tuberolactone; terpenes such as for example linalool, citral, geranial, neral, menthol, cymol, myrcene, carene, cineol, sabinene, pinene-alpha, pinene-beta, citronellol, geraniol, terpineol, bisabolene, caryopyllene, farnesol, farnesene, carvone, camphene, citronellal, citral, eucalyptol, linalool oxide, menthol, nerol, phellandrene, pulegone, pulegol, sinensal, limonene, thymol, valencene, isopulegone; sulfides and disulfides such as for example dimethyl sulfide, difurfuryl disulfide, methylthio propanal; thiols such as for example methyl furanthiol, benzothiazole, isopropyl methyl thiazole, sulfurol, 8,3-thiomenthanone, 4,4,2-thiomethyl pentanone, 2,4,5-trimethyl thiazole, 2-acetylthiazole, 2,4-dimethyl-5-ethylthiazole; pyrazines and pyrrolines such as for example methyl pyrazine, acetyl pyrazine, 2- propionyl pyrroline, 2-acetyl pyrroline, 2-acetyl-1-pyrroline, 2-methyl-3-ethylpyrazine, 2- ethyl-3,5-dimethylpyrazine, 2-ethyl-3,6-dimethylpyrazine, 2,3-diethyl-5-methylpyrazine, 3- isopropyl-2-methoxypyrazine, 3-isobutyl-2-methoxypyrazine, 2-pentylpyridin; as well as (not explicitly named herein) stereoisomers, enantiomers, positional isomers, diastereomers, cis/trans-isomers and epimers of these substances.

Flavouring substances can also directly influence the taste (taste modulators) and can be, for example, selected from the group consisting of monosodium glutamate, free glutamic acid, nucleotides or pharmaceutically acceptable salts thereof, strombines, theogallines such as described in JP 2007 1 10988 A, pyridine-betaine-compounds such as described in EP 1291342 B1 , glutamic acid glycosides such as described in WO 2002 087361 A1 , malic acid glycosides such as described in WO 2006 003107 A1 , glutathion- derivates such as described in EP 0181421 or WO 2007 042273 A1 , alkyl pyridines (preferably alkyl pyridines such as described in WO 2009 122318 A1 and WO 2009 1223319 A1 ), particularly 2-hexyl-, 2-heptyl and 2-octylpyridine, (2E,6Z)-N- cyclopropylnona-2,6-dienamide, (2E,6Z)-N-ethylnona-2,6-dienamide, N-[(2E)-3,7- dimethylocta-2,6-dienyl]cyclopropancarboxamide, N'-[(2-methoxy-4-methyl- phenyl)methyl]-N-[2-(5-methyl-2-pyridyl)ethyl]-oxamide, N'-[(2,4- dimethoxyphenyl)methyl]-N-[2-(2-pyridyl)ethyl]oxamide, N'-[(2-methoxy-4-methyl- phenyl)methyl]-N-[2-(2-pyridyl)ethyl]oxamide, N-(1-propylbutyl)-1 ,3-benzodioxole-5-carb- oxamide, 1-(2-hydroxy-4-isobutoxy-phenyl)-3-(2-pyridyl)propan-1-one and 1-(2-hydroxy- 4-methoxy-phenyl)-3-(2-pyridyl)propan-1-one, cinnamic acid amides such as described in EP 2529632 B1 or WO 2013 000,673), lactisole, hesperitin according to EP 1909599 A1 , phloretin according to EP 1972203 B1 or EP 1998636 B1 , hydroxyflavane according to US 2010 292175 AA, 4-hydroxychalcone according to EP 1972203 B1 , extracts on the basis of hydrangea dulcis according to EP 2298084 A2, or rubus ssp.; mixtures of whey proteins with lecithines, yeast extracts, plant hydrolysates, pulverised vegetables (e.g. onion powder, tomato powder), plant extracts (e.g. of lovage or of mushrooms such as shiitake), seaweed and mineral salt mixtures, particularly mineral salt mixtures according to US 2009 214728 AA, rubemamine or rubescenamine according to EP 2529632 B1.

A preferred embodiment of a mixture according to the invention is a liquid form, particularly a form that can be incorporated into a preparation according to the invention (as described herein and further below).

Furthermore, a mixture according to the invention can also be transferred into a solid form, e.g. by means of spray drying, or can be present in solid form. Methods suitable therefore are sufficiently known to the skilled person. As mentioned above, mixtures and flavouring compositions according to the invention, respectively, advantageously are suitable to be used in and incorporated into, respectively, a multitude of different preparations. Accordingly, the present invention also relates to a preparation, preferably a preparation for nourishment or pleasure, a preparation for animal feeding, a cosmetic preparation, a preparation for oral care or a pharmaceutical preparation for oral intake, comprising a mixture according to the invention as well as one or more further components.

Preferably, the or one, several or all of the components, respectively, are selected from the group consisting of oxidation-sensitive compounds, particularly such compounds that are sensitive towards autoxidation (cf. hereto above). In light of the explanations above, it is of course particularly advantageous when the mixture according to the invention in the preparation according to the invention is comprised in an amount to reduce, avoid or delay the formation of sensorially undesired flavours and/or tastes in oxidative degradation processes or autoxidative processes or to reduce, avoid or delay oxidative processes in one or more oxidation-sensitive compounds, particularly autoxidative processes, and/or in an amount that is anti- autoxidatively effective. That is, (a) preferably the preparation has a higher Folin- Ciocalteu value than a preparation without the mixture according to the invention, but with an otherwise identical composition, and/or (b) preferably the amount of mixture according to the invention is sufficient to slow down or to reduce or to avoid altogether, respectively, oxidation or autoxidation, respectively, of one or more other substances comprised in the preparation (cf. hereto also example 2, comparison of the amount of formed degradation products).

In principle, what has been stated above with regard to preferred mixtures according to the invention also applies to mixtures preferably comprised in a preparation according to the invention. That is, a preparation according to the invention preferably comprises a mixture according to the invention that has been described above as preferred within the scope of the present invention.

Preferably, the total amount of mixture according to the invention in the preparation according to the invention is less than 5 wt.-%, preferably less than 3 wt.-%, particularly preferably less than 1 wt.-%, especially preferably less than 0.5 wt.-%.

For the production of a preparation according to the invention the required components can be mixed, whereby the components can be present in the form of solids, solutions, extracts, aqueous extracts as well as enriched preparations and concentrates, respectively, for example, by means of distillation, chromatography or Symtrap®. The Symtrap® method is a method of enrichment for the production of a flavour concentrate, which is described in document EP 2075321 B1.

The present invention also relates to a method of producing a preparation according to the invention, comprising or consisting of the following steps:

(i) provision of a mixture according to the invention, preferably of a mixture as described herein as preferred, or provision of the components a) to h) as well as optionally i), j) and k) of a mixture according to the invention, preferably of a mixture as described herein as preferred,

(ii) provision of one or more further components, and

(iii) mixing of the components provided in steps (i) and (ii).

According to a preferred embodiment, a preparation according to the invention is a preparation for nourishment or pleasure for example selected from baked goods (e.g. bread, dry biscuits, cake, other pastries), confectionery (e.g. chocolates, fillings, chocolate bar products, other bar products, candy, fruit gum, hard- and soft caramels, chewing gum), alcoholic and non-alcoholic beverages (e.g. coffee, tea, wine, wine-based beverages, beer, beer-based beverages, liqueurs, schnapps, brandy, fruit lemonades, isotonic beverages, soft drinks, nectars, fruit- and vegetable juices, fruit- and vegetable juice preparations), instant beverages (e.g. instant hot chocolate beverages, instant tea beverages, instant coffee beverages), solid or powdery instant products and instant spice mixes (e.g. spice mixes and stocks), liquid or paste-like spice mixes (e.g. meat stocks, concentrates, flavours, seasoning sauces), meat products (e.g. ham, fresh sausage- or raw sausage preparations, seasoned or marinated fresh- or salt meat products), eggs or egg products (dehydrated egg, egg white, egg yolk), cereal products (e.g. breakfast cereals, muesli bars, pre-cooked instant rice products), milk products (e.g. milk drinks, milk icecream, joghurt, kefir, cream cheese, soft cheese, hard cheese, dried milk powder, whey, butter, buttermilk, partly or fully hydrolysed milk protein-containing products), products made from soy protein or other soybean fractions (e.g. soy milk and products manufactured thereof, soy lecithin-containing preparations, fermented products such as tofu or tempe or products produced thereof, soy sauces), fruit preparations (e.g. jams, fruit icecream, fruit sauces, fruit fillings), vegetable preparations (e.g. ketchup, sauces, dehydrated vegetables, deep frozen vegetables, pre-cooked vegetables, vegetables marinated in vinegar, boiled down vegetables), snack articles (e.g. baked or deep-fried potato chips or potato dough products, bread dough products, extrudates, for example on corn- or peanut basis), products on fat- and oil basis or emulsions thereof (e.g. remoulade, mayonnaises, bechamel, hollandaise, aioli, mustard, chutneys, dips, sauces, dressings, spice preparations), other ready meals and soups (e.g. dried soups, instant soups, pre-cooked soups), spices, spice mixtures as well as particularly seasonings that, for example, are used in the snack area. The preparations according to the invention can also serve as intermediate goods for producing further preparations for nourishment or pleasure. The preparations according to the invention can also be present in the form of capsules, tablets (non-coated as well as coated tablets, e.g. with enteric coating), lozenges, granulates, pellets, solid mixtures, dispersions in liquid phases, as emulsions, as powders, as solutions, as pastes or as other swallowable or chewable preparations as dietary supplements.

According to a further preferred embodiment, a preparation according to the invention is a pharmaceutical preparation destined for oral intake, e.g. in the form of capsules, tablets (non-coated as well as coated tablets, e.g. with enteric coating), lozenges, coatings and swallowing aids for tablets and capsules, granulates, pellets, solid mixtures, dispersions in liquid phases, as emulsions, as powders, as solutions, as pastes or as other swallowable or chewable preparations and as pharmacy-only drugs, drugs available only on prescription, or other drugs or as dietary supplements.

According to another preferred embodiment, a preparation according to the invention is a preparation for oral care, e.g. selected from the group consisting of oral and/or dental care agents such as tooth pastes, tooth gels, tooth powders, mouthwashes, chewing gums and other oral care agents.

According to another preferred embodiment, a preparation according to the invention is a cosmetic preparation. Preferred cosmetic preparations within the scope of the present invention are in particular cosmetic preparations for application in the area of the head, preferably cosmetic preparations that can get in contact with the oral cavity even if applied correctly. Such preparations are, for example, soaps, other cleaning or care agents for the facial area, facial cremes, -lotions or -ointments, sun protection agents, beard cleaning or care agents, shaving foams, -soaps or -gels, lip sticks or other lip cosmetics or lip care agents.

Preparations according to the invention can also comprise (other) common raw materials, excipients and additives, e.g. - in particular so for preparations serving nourishment or pleasure - (additional) water, mixtures of fresh or processed plant-based or animal-based raw materials (e.g. raw, fried, dried, fermented, smoked and/or cooked meat, bones, cartilage, fish, vegetables, fruits, herbs, nuts, vegetable- or fruit juices or -pastes or mixtures thereof), digestible or non-digestible carbohydrates, sugar alcohols (e.g. sorbit, erythritol), natural or hardened fats (e.g. tallow, lard, palm fat, coconut oil, hardened vegetable fat), oils (e.g. sunflower oil, peanut oil, corn oil, olive oil, fish oil, soy oil, sesame oil), fatty acids and salts thereof (e.g. potassium stearate), proteinogenic or non- proteinogenic amino acids and related compounds (e.g. gamma-amino butyric acid, taurine), peptides (e.g. glutathione), native or processed proteins (e.g. gelatin), enzymes and/or coenzymes (e.g. peptidases), nucleic acids, nucleotides, taste correctors or taste modulators, respectively, for unpleasant taste impressions or not unpleasant taste impressions, in particular taste-modulating substances (e.g. inositol phosphate, nucleotides such as guanosine monophosphate, adenosine monophosphate or other substances such as sodium glutamate or 2-phenoxypropionic acid), emulsifying agents (e.g. lecithins, diacylglycerols, gum arabic), stabilisers (e.g. carageenan, alginate), preservatives (e.g. benzoic acid, sorbic acid), further antioxidants, stabilisers, further organic or inorganic acidifying agents, bitter agents if applicable (e.g. quinine, caffeine, limonin, amarogentin, humolone, lupolone, catechins, tannins), sweeterners if applicable (e.g. saccharin, cyclamate, aspartame, neotame), mineral salts (e.g. sodium chloride, potassium chloride, magnesium chloride, sodium phosphate, calcium chloride), vitamins, substances avoiding enzymatic browning (e.g. sulfite, ascorbic acid), essential oils, plant extracts, natural or synthetic dyes or dye pigments (e.g. carotinoids, flavonoids, anthocyanes, chlorophyll and derivatives thereof), spices, trigeminally active substances or plant extracts comprising such trigeminally active substances, further synthetic, natural or nature-identical flavouring substances or aroma substances or fragrance substances as well as odour correctors. Tooth care agents (as example for preparations according to the invention serving oral care; cf. above), usually comprise an abrasive system (abrasives or polishing agents), such as e.g. silicic acids, calcium carbonates, calcium phosphates, aluminum oxides and/or hydroxyapatites, surfactants such as e.g. sodium lauryl sulfate, sodium lauryl sarcosinate and/or cocamidopropylbetaine, humectants such as e.g. glycerine and/or sorbitol, thickening agents such as e.g. carboxymethyl cellulose, polyethylene glycols, carrageenans and/or Laponite^®, sweeteners if applicable such as e.g. saccharin, taste correctors for unpleasant taste impressions or usually not unpleasant taste impressions, taste-modulating substances (e.g. inositol phosphate, nucleotides such as guanosine monophosphate, adenosine monophosphate or other substances such as sodium glutamate or 2-phenoxypropionic acid), cooling agents such as e.g. menthol, menthol derivates (e.g. L-menthol, L-menthyl lactate, L-menthyl alkyl carbonates, menthone ketals, menthane carboxylic acid amides), 2,2,2-trialkyl acetic acid amides (e.g. 2,2- diisopropyl propionic acid methylamide), icilin derivatives, stabilisers and active agents such as e.g. sodium fluoride, sodium monofluorophosphate, tin difluoride, quarternary ammonium fluorides, zinc citrate, zinc sulfate, tin pyrophosphate, tin dichloride, mixtures of different pyrophosphates, triclosan, cetylpyridinium chloride, aluminium lactate, potassium citrate, potassium nitrate, potassium chloride, strontium chloride, hydrogen peroxide, (further) flavours and/or sodium bicarbonate or odour correctors.

Chewing gums (as further or specific example, respectively, for preparations according to the invention serving oral care; cf. above), usually comprise a chewing gum base, that is a chewable base that becomes malleable during mastication, sugar of different kinds, sugar substitutes, sweeteners, sugar alcohols, taste correctors or taste modulators, respectively, for unpleasant taste impressions or usually not unpleasant taste impressions, taste-modulating substances (e.g. inositol phosphate, nucleotides such as guanosine monophosphate, adenosine monophosphate or other substances such as sodium glutamate or 2-phenoxypropionic acid), humectants, thickeners, emulifiers, (further) flavours and stabilisers or odour correctors.

As further components for oral pharmaceutical preparations according to the invention (cf. above) mainly all of the commonly used active substances, raw materials, excipients, and additives can be used for pharmaceutical preparations provided for oral application. The active substances, raw materials, excipients, and additives can be transformed into application forms suitable for oral application according to known methods. This usually happens by means of using inert, non-toxic, pharmaceutically suitable excipients. This includes, amongst others, carrier substances (e.g. microcrystalline cellulose), solvents (e.g. liquid polyethylene glycols), emulsifiers (e.g. sodium dodecyl sulfate), dispersing agents (e.g. polyvinyl pyrrolidone), synthetic and natural biopolymers (e.g. albumin), stabilisers (e.g. antioxidants), dyes (e.g. inorganic pigments such as iron oxides) and odour correctors as well as taste correctors.

Preferably, preparations according to the invention (as described above) can contain a further flavor composition (not according to the invention) to (further) round off or refine the sensorial impression of the preparation. Suitable flavour compositions comprise e.g. synthetic, natural or nature-identical flavouring substances as well as suitable excipients and carrier substances.

From the above explanations in connection with the mixtures according to the invention described herein it becomes clear that they are also suitable for use as oxidation- decelerating or oxidation-inhibiting effective substance, particularly as anti-autoxidative effective substances. Particularly preferable is thereby the use of a mixture according to the invention in a preparation according to the invention (as described herein). It is thereby particularly advantageous, if the mixture according to the invention leads to (a) that the preparation comprising the mixture has a higher Folin-Ciocalteu value than a preparation without the mixture according to the invention, but with an otherwise identical composition, and/or (b) that the amount of mixture according to the invention (in the preparation) is sufficient to slow down or to reduce or to avoid altogether, respectively, an oxidation or autoxidation, respectively, of one or more other substances (comprised in the preparation) (cf. hereto also example 2, comparison of the amount of formed degradation products).

In this context, the present invention also relates to a method for reducing, avoiding or delaying the formation of sensorially undesired flavours and/or tastes in oxidative degradation processes or autoxidative processes or reducing, avoiding or delaying of oxidative processes in one or more oxidation-sensitive compounds, particularly autoxidative processes, comprising or consisting of the following steps:

(A) Provision of a mixture according the invention or provision of the components a) to h) as well as optionally i), j) and k) of a mixture according to the invention,

(B) provision of one or more further components, wherein the or one, several or all of the further components, respectively, is or are selected from the group consisting of oxidation-sensitive compounds, particularly those that are sensitive towards autoxidation, and

(C) contacting, preferably mixing, of the components provided in steps (A) and (B).

(cf. hereto also example 2, comparison of the amount of formed degradation products).

In terms of preferred embodiments of the method according to the invention, what has been stated above, in particular in connection with preferred embodiments of mixtures and preparations according to the invention, applies accordingly.

In the following, the present invention will be further described with the aid of selected, specific examples. The examples only serve to clarify the invention without limiting the invention or limiting it thereto. All specifications relate to the weight, unless indicated otherwise.

Examples:

Example 1 : Mixtures (according to the invention)

Table: Mixture examples M1 to M6

For production, the solid ingredients are solved in the premixed solvents water and PG. If necessary, this preparation is slightly heated to max. 40 °C until everything is solved. Then the other ingredients were added after cooling to room temperature. Example 2: Dressing (A, B: comparative examples; C: according to the invention)

Table: Dressing

A B c

Component wt.-% wt.-% wt.-%

Sunflower oil 42.00 42.00 42.00

Water 25.26 25.16 25.16

Egg yolk, pasteurised 18.90 18.90 18.90

Vinegar 5% 5.91 5.91 5.91

Mod. corn starch C*Tex06205 4.15 4.15 4.15

Sucrose 2.30 2.30 2.30

Salt 1.38 1.38 1.38

Guar gum 0.10 0.10 0.10

Calcium-Disodium EDTA 0.10

Mixture M5 according to example 1 - - 0.10

Sum 100.00 100.00 100.00

For production, the dry components are added to the water first and heated to 90 °C, whereby this temperature is then kept for 3 minutes. Subseguently, the temperature is cooled to 25 °C and for sample B the EDTA and for sample C the mixture according to example 1 are added, respectively until everything is fully dissolved. Then the oil, the vinegar and the egg yolk are added. Subseguently, the preparations are homogenized with a high pressure homogenizer at 180 bar.

Stability test:

Samples of preparations A, B and C were stored at 50 °C for 7 days in the heating cabinet to stimulate, to force and to investigate the oxidative and autoxidative processes, respectively. Analytical testing:

Analytical testing was carried out by means of Symstixx and GC-MS. A detailed description of the Symstixx® method is described in document EP 2233206 A1. The GC- MS measurement was carried out with a VF-Wax mx separating column (30m x 0.25mm x 0.25mm) and a temperature program of 40°C-3°C/min-230°C. During the measurements carried out, the substances hexanal, ir-2-octenal, 1 ,3-octenone, tr-2- heptenal, 2E,4Z-heptadienal, ir,ir-2,4-heptadienal, 2E-decenal, 2E,4E-decadienal, 2E,4E,7Z-decatrienal and 2E,4Z,7Z-undecatrienal that are typical for oxidative processes were determined. The determination of the amounts of these substances took place by means of the internal standard 2-nonanol. The determined ppm-amounts of these substances were summed up and the total amount of degradation substances was determined. The measured total amounts of sample A, sample B and sample C were compared to each other and the percentage ratio with regard to sample B was calculated.

Table : Results of the analytical measurements

A B C

ppm ppm ppm

Total amount degradation substances 16512 5791 3984

percentage ratio in comparison w ith sample B 31

The results show that sample A exhibits a considerably higher total amount of degradation substances than the other samples, wherein sample C with the mixture according to the invention displayed the lowest total amount of degradation substances. The measured total amount of degradation substances of sample C was 31 % lower than the total amount of degradation substances of sample B with EDTA.

Example 3: Mayonnaise

Table: Mayonnaise

Component wt.-%

Sunflower oil 79.20

Water 7.40

Egg yolk, pasteurised 6.00

Vinegar 5% 4.00

Sugar 1.50

Table salt 1.00

Mixture M2 according to example 1 0.80

flavour 0.10

Sum 100.00

For production of the mayonnaise, the water, vinegar, sugar, salt, mixture M2 and flavour are mixed first. Then one third of this mixture is mixed with the egg yolk. To this mixture, the oil is added with a weak jet, slowly in the beginning and faster towards the end, with simultaneous strong emulsification work. In between and mainly towards the end, the remaining amount of the mixture of water, vinegar, sugar, salt, mixture M2 and flavor are added between two portions of oil.

Example 4: Seasoning

Table: Cheese seasoning

Component wt.-%

Cheddar type cheese flavour SD 2.00

Citric acid 0.30

Lactic acid powder (loading 60% lactic acid) 1.00

Fat powder (Loading 77% fat) 9.75

Cheese powder mild cheddar type 11.75

Mixture M5 according to example 1 1.00

Yeast extract powder 5.00

Salt for seasonings 21.50

Onion powder 3.00

Cream powder (43% fat) 1.50

Silicon dioxide 0.70

Curcuma extract in vegetable oil 0.50

Vegetable oil triglycerides/coconut oil 0.30

Lactose/milk sugar 100 mesh vegetarian 20.00

Glucose/Dextrose (Corn IP) 8.00

Wheat powder vegetarian 13.70

Sum 100.00

First the crystalline substances are added to the liquid components and mixed until everything is uniform. Then the remaining dry components and the concentrates are added and mixed until everything is homogeneous.

Example 5: Milk fat filling

Component wt.-%

Dextrose 10.00

Icing sugar 32.70

Vegetable fat 39.50

Skim milk powder 8.00

Whole milk powder 8.70

Mixture M4 according to example 1 0.80

Lecithin 0.30

Sum 100.00 All components apart from half of the fat are mixed with each other. The refiner with three rollers should be used with a pressure setting of 60-75 bar for the input roller and of 1 10- 125 bar for the output roller. Then the preparation is homogenized in the refiner. Subsequently, the remaining fat is introduced and mixed, respectively, with the aid of a mixer until the preparation is homogeneous.

Example 6: Biscuits

Table: Biscuits

Component wt.-%

1 Wheat flour type 550 48.45

2 Vegetable fat Bavetin 28090 LT 19.50

3 Sugar 19.50

4 Eggs 5.00

5 Water 5.00

6 Skim milk powder 1.00

7 Mixture M1 according to example 1 1.00

8 Iodised salt 0.30

9 Ammonium bicarbonate 0.25

Sum 100.00

First, component No. 9 is dissolved in water and an elastic dough is formed from all of the components. Then the dough is cooled for 30 minutes and then rolled out to 2.75 mm. Subsequently, the dough is baked at 190 °C heat from above and at 200 °C heat from below for 8 minutes.

Example 7: Cracker

Table: Cracker

Component

Phase A

1 Wheat flour type 550 57.18

2 Wheat starch 6.00

3 Glucose syrup C Sweet M 01415 6.00

4 Vegetable fat Biscuitine 200 10.00

5 Iodised salt 1.00

6 Ammonium bicarbonate 1.40

7 Baking powder 0.30

8 Eggs 5.00

9 Water 13.00

10 Lecithin 0.10

1 1 Enzyme Sternzym BK Quick 0.02

Phase B

1 Vegetable fat or vegetable oil 98.90

2 Mixture M2 according to example 1 1.00

3 Aroma 0.10

Sum 100.00

Phase A: First the ammonium bicarbonate is dissolved in water. Then the remaining components are mixed and then the mixture of water and ammonium bicarbonate is added. After the dough was kneaded in a Z-kneader for 6-8 minutes, it is brought to a temperature of 40 °C. After a resting time of 30-60 minutes, the dough is rolled out to 1.75 mm and cut into 5 x 5 cm sized pieces. Then the pieces are baked at a heat from above of 300 °C and a heat from below of 260 °C for 3 minutes under steaming. After baking, the pieces are baked for a second time at a heat from above of 170 °C and a heat from below of 170 °C for 3 minutes and dried at 120 °C for 5 minutes. For production of phase B, the fat is melted, then the aroma and mixture M2 are added and homogenized. 8-10% of phase B are sprayed onto the dry crackers. Example 8: Make-up remover

Table: Make-up remover

Component INCI wt.-%

Phase A

Glycerin Glycerin 9.30

Surfhope® C-1216 Sucrose La urate 3.00

Surfhope® C-1616 Sucrose Pa Imitate 3.00

Water Water (Aqua) 4.70

Phase B

Neutral oil Caprylic/Capric Triglyceride 47.71

Dragoxat® 89 Ethylhexyl Isononanoate 30.00

lonol CP BHT 0.05

Phase C

Symdiol® 68 1 ,2-Hexanediol, Caprylyl Glycol 0.80

Phase D

Perfume Parfum 0.15

Mixture M3 according to example 1 1.00

Colour system I Colour 0.15

Colour system II Colour 0.14

Sum 100.00

The production takes place in a Becomix.

For production of phase A, the glycerin and Surfhope® C1216 are put into the Becomix and are stirred at -0.5 bar with 0.3 m/s, then they are homogenized with the aid of a Turrax at 3 m/s for 4 minutes. When the Surfhope® C1216 is completely dissolved, the Surfhope® C1616 is added, whereby the stirring is continued at 0.3 m/s. The subsequent homogenization takes place at 3 m/s for 4 minutes with the aid of a Turrax. Then water is added and again homogenized with the aid of a Turrax at 3 m/s for 6 minutes. This mixture is heated to 80 °C under stirring at 0.3 m/s, then brought to 50 °C and again homogenized with the aid of a Turrax with 3 m/s for 2 minutes. Subsequently, the temperature is raised to 80 °C and a pressure of -0.6 bar is adjusted.

The production of phase B takes place at 80 °C. At a temperature of 80 °C, the components of phase B are very slowly and consecutively mixed with each other and then stirred at 0.5 m/s as well as homogenized with the aid of a Turrax at 3 m/s for 2 minutes. When one quarter of the oil has been put into the boiler, a homogenization step takes place with the aid of a Turrax at 5 m/s for 4 minutes. After half of the oil has been added, it is homogenized again with the aid of a Turrax at 5 m/s for 4 minutes and the stirring speed is raised to 0.8 m/s. When three quarters of the oil have been added, a homogenization step with the aid of a Turrax at 5 m/s for 4 minutes and an increase of the stirring speed to 1 m/s follow. Then the remaining amount of the oil is added and stirred at 1 .2 m/s.

After addition of phase C, the pressure is raised to -0.8 bar and it is homogenized with the aid of a Turrax at 5 m/s for 4 minutes. The preparation is cooled under stirring at 0.5 m/s to 25 °C, whereby the stirring speed is reduced. Then phase D is added at 40°C.

Colour system I: 0.1 % solution in isopropyl palmitate of D&C Red N °17 C.I. 26100 Colour system II: 0.1 % solution in isopropyl palmitate of Phat Brown DC 8206: C.I. 47000, C.I. 26100, C.I. 60725

The final preparation has a viscosity of 69280cP.

Example 9: Lip care stick Table: Lip care stick

Component INCI wt.-%

Medium mineral oil Paraffinium Liquidum 26.00

Permulgin 3220 Ozokerite

20.00

Paraffin 52-54 Paraffin

12.00

Neutral oil Caprylic/Capric Triglyceride

9.95

Mixture M1 according to example 1

0.05

Prisorine Sqs 3758 Hydrogenated Polyisobutene

5.00

Cetiol 868 Ethylhexyl Stearate

5.00

Softisan 100 Hydrogenated Cocoglycerides

5.00

Xiameter® PMX-0245 Cyclosiloxane Cyclopentasiloxane

4.00

Elfacos E 200 Methoxy PEG-22 and Dodecyl Glycol Copolymer

4.00

Permulgin 3430 Copernicia Cerifera (Carnauba) Wax

2.00

Ivarlan 3360 Glyceryl Lanolate

3.00

Super Hartolan Lanolin Alcohol

1.40

Cutina® FS 45 Stearic acid, Palmitic acid

1.50

Jojoba oil 1.00

Titanium dioxide Titanium Dioxide 0.10

Perfume Perfume 0.01

Sum 100.00 For production, all of the components in the order of the list without the perfume are melted and homogenized during warming to 70 °C. At a temperature of 50 °C, the perfume is added and homogenized.

Examplel O: Night cream

Table: Night cream

Component INCI wt.-%

Phase A

Dragosan W/O P Sorbitan Isostearate, Hydrogenated Castor oil, 5.00

Beeswax (Cera Alba)

Medium Mineral Oil Paraffinium Liquidum 15.00 Vaseline Petrolatum 4.50

Tece Ozokerit N 325/11 Ozokerite 2.30 Dragoxat® 89 Ethylhexyl Isononanoate 5.00

Phase B

Water Water (Aqua) 64.10

Glycerin, 99,5 P. Glycerin 3.00 Magnesiumsulfate

Magnesium Sulfate 0.70 Heptahydrate

Preservative Complex (ND Triethylene Glycol, Imidazolidinyl Urea, 0.30 Liquid) Methylparaben, Propylparaben, Dehydroacetic

acid

Phase C

Perfume Perfum 0.10

Mixture M3 according to

0.50 example 1

Sum 100.00

For production, phase A and phase B are separately warmed to 80 °C, respectively. Then phase B is added to phase A while using an Ultra-Turrax and emulsified. While stirring with a paddle agitator, this mixture is cooled and then emulsified again at 60 °C. When the mixture has reached a temperature of about 35 °C, phase C is added.

Claims

Patent claims

1. Mixture comprising or consisting of a) one or more monocyclic monoterpenes of formula (I)

(I) with R1 = hydrogen, hydroxy group or carbonyl group, R2 = hydrogen, hydroxy group or carbonyl group, R3 = 0, hydrogen or hydroxy group and R4 = isopropyl group, isopropenyl group or isopropylidene group as well as without or with one, two or three double bonds in the cyclic system, preferably selected from the group consisting of gamma-terpinene, alpha- terpinene, beta-terpinene, beta-phellandrene, limonene, thymol, pulegone, carvacrol and alpha-phellandrene, one or more benzoic acid derivatives of formula (II)

(II) with R1 , R2 and R3 independently of each other selected from the group consisting of hydrogen, hydroxy group and methoxy group, c) a first 3-phenylpropenoic acid derivative of formula (IV)

(IV) with R1 = 1-carboxy-2-(3,4-dihydroxyphenyl)ethyl, R2 = hydrogen and R3 = hydrogen,

optionally a second 3-phenylpropenoic acid derivative of formula (IV) with R1 = 5-carboxy-2,3,5-trihydroxycyclohexyl, R2 = hydrogen and R3 = hydrogen, and

optionally a third 3-phenylpropenoic acid derivative of formula (IV) with R1 = hydrogen, R2 = hydrogen and R3 = hydrogen, tartaric acid (formula (V))

D-(-)-form, and/or L-(+)-form, and/or meso-form

(V), citric acid (formula (VI)) and/or malic acid (formula (VII))

f) glucose, fructose and/or sucrose, g) 1 ,2-propanediol and/or 1 ,3-propanediol and/or propane-1 ,2,3-triol h) water, i) optionally gallocatechin (Formula (III))

(2R,3S)-3,4-dihydro-2-(3,4,5-trihydroxyphenyl)-2H-1-benzopyran-3,5,7-triol

2. Mixture according to claim 1 , wherein the mixture has an ORAC value of greater than 200 μιηοΙ TE/g, with respect to the dry weight of the mixture, preferably of greater than 500 μιηοΙ TE/g, particularly preferably of greater than 1000 μιηοΙ TE/g, especially preferably of greater than 2000 μιηοΙ TE/g.

3. Mixture according to claim 1 or 2, wherein the mixture has a polyphenol content according to Folin-Ciocalteu of greater than 5 %, with respect to the dry weight of the mixture, preferably of greater than 10 %, particularly preferably of greater than 15 %.

4. Mixture according to any of the preceding claims, comprising or consisting of, with regard to the total weight of the mixture, respectively,

0.0001 to 80 wt.-% of component a), preferably 0.001 to 10 wt.-%, particularly preferably 0.01 to 5 wt.-%, especially preferably 0.1 to 1 wt.-%,

%

0.0001 to 1 wt.-% of component i), preferably 0.001 to 0.7 wt.-%, particularly preferably 0.005 to 0.

5 wt.-%, especially preferably 0.01 to 0.15 wt.-%

Mixture according to any of the preceding claims, wherein the mixture is a flavour

6. Preparation, preferably preparation for nourishment or pleasure, preparation for animal feeding, cosmetic preparation, preparation for oral care or pharmaceutical preparation for oral intake, comprising a mixture according to any of the preceding claims as well as one or more further components.

7. Preparation according to claim 6, wherein the or one, several or all of the further components, respectively, is/are selected from the group consisting of oxidation-sensitive compounds, particularly those that are sensitive towards autoxidation.

8. Preparation according to claim 6 or 7, wherein the mixture according to any of the claims 1 to 5 is contained in the preparation in an effective amount to reduce, avoid or delay the formation of sensorially undesired flavours and/or tastes in oxidative degradation processes or autoxidative processes or to reduce, avoid or delay oxidative processes in one or more oxidation-sensitive compounds, particularly autoxidative processes, and/or in an amount that is effective anti-autoxidatively.

9. Preparation according to any of the claims 6 to 8, wherein the total amount of mixture according to any of the claims 1 to 5 in the preparation, with regard to the total weight of the preparation, is less than 5 wt.-%, preferably less than 3 wt.-%, particularly preferably less than 1 wt.-%, especially preferably less than 0.5 wt.-%.

10. Method of producing a preparation according to any of the claims 6 to 9, comprising or consisting of the following steps:

(i) provision of a mixture according to any of claims 1 to 5 or provision of the components a) to h) as well as optionally i), j) and k) of a mixture according to any of the claims 1 to 5,

(ii) provision of one or more further components, and

(iii) mixing of the components provided in steps (i) and (ii).

1 1. Use of a mixture according to any of the claims 1 to 5 as component in a preparation according to any of the claims 6 to 9.

12. Method for reducing, avoiding or delaying the formation of sensorially undesired flavours and/or tastes in oxidative degradation processes or autoxidative processes or reducing, avoiding or delaying of oxidative processes in one or more oxidation-sensitive compounds, particularly autoxidative processes, comprising or consisting of the following steps:

(A) provision of a mixture according to any of the claims 1 to 5 or provision of the components a) to h) as well as optionally i), j) and k) of a mixture according to any of the claims 1 to 5,

(B) provision of one or more further components, wherein the or one, several or all of the further components, respectively, is/are selected from the group consisting of oxidation-sensitive compounds, particularly those that are sensitive towards autoxidation, and