US 4,200,659 AGrant
Flavoring Compositions Containing Dialkyl-.Alpha.,.beta.-Diacyl Succinates
Issue Date:1980-04-29
•7 Claims
Abstract
The flavor compositions of this invention include certain dialkyl-.alpha.,.beta.-diacyl succinates which significantly enhance the flavor component or components of flavor compositions. For example, butterscotch flavors are materially improved in smoothness and certain fruit flavors are given greater richness and ripeness.
Metadata
Assignee
- Fritzsche Dodge & Olcott Inc.
Inventors
- Brian J. Willis
- Frank Fischetti, Jr.
- Robert G. Eilerman
Application Information
Application Number:US 9191372
Filing Date:1978-06-26
Priority Date:1975-08-06
Art Unit:172
Classifications
IPC:
A23L 1226
Field of Search:
426534;538
Patent Drawings
This patent does not have any drawings.
Description
This invention relates to flavor compositions and more particularly to flavor compositions containing certain dialkyl-.alpha.,.beta.-diacyl succinates.
It is well known that synthetic flavor echancers such as Maltol, Ethyl Maltol, and 4-hydroxy-2,5-dimethyl-3(2H)-furanone are useful as flavor enhancers. However, such flavor enhancers are very expensive and increase the cost of products in which they are used.
In accordance with this invention, dialkyl-.alpha.,.beta.-diacyl succinates are added to flavor components to impart significantly enhanced flavors to a wide variety of flavor components. For example, butterscotch flavors are materially improved in smoothness. Strawberry flavors are given a striking freshness. Banana flavors are rounded out to give the flavor of a ripe banana. When added to smoking tobacco or synthetic tobacco, the resulting product is increased in sweetness, the taste of the smoke is softened and the flow of saliva is increased, which lessens dryness of the mouth during smoking. When added to cough syrups containing theophylline, the flavor enhancers of this invention cover up the bitter taste. These flavor enhancers can also be used to replace part of the sugar content of a wide variety of sweetened beverages and foods, producing excellent flavor at lower cost.
The dialkyl-.alpha.,.beta.-diacyl succinates employed in the flavor compositions of this invention have the formula: ##STR1## in which R.sub.1 is a straight or branched chain alkyl having less than 6 carbon atoms or cyclohexyl and R.sub.2 is a straight or branched chain alkyl having less than 7 carbon atoms, cyclopentyl or cyclohexyl.
Examples of R.sub.1 are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, amyl or isoamyl.
Examples of R.sub.2 are methyl, ethyl, propyl, isopropyl, butyl, isobutyl, amyl, isoamyl, hexyl or isohexyl.
R.sub.1 and R.sub.2 may be the same or different.
When R.sub.2 is ethyl or methyl, the succinate is prepared by the method described by M. S. Newman and J. S. Cella, J. Org. Chem. 38, 3482 (1973). When R.sub.2 is other than ethyl or methyl, and R.sub.1 is other than methyl, the procedure is the same except that the appropriate .beta.-ketoesters are used instead of the acetoacetic esters.
The flavor compositions of this invention comprise at least 0.0025% by weight of a dialkyl-.alpha.,.beta.-diacyl succinate. The total amount of dialkyl-.alpha.,.beta.-diacyl succinate or succinates may vary within wide ranges such as 0.0001% to 30% by weight. More advantageously the range may be between 0.001% and 20% by weight of the flavor composition and preferably between 0.0025% and 5% by weight of the flavor composition.
Examples of flavor components of the flavor compositions of this invention are flavor mixtures per se such as pineapple, butterscotch, banana, and strawberry; foodstuffs such as meats, protein sources, fruits, cereals and other comestibles; beverages such as soft drinks, wines, alcoholic drinks, carbonated beverages; smoking tobacco; liquid medicaments such as cough syrups; and sugar substitutes in a wide range of edible or drinkable products.
A more comprehensive understanding of this invention is obtained from the following examples. Examples I and II show compositions produced with two levels of concentration of the dialkyl-.alpha.,.beta.-diacyl succinate employed.
Example I
Example Ii
Example Iii
Example Iv
Example V
Formulas VA and VB contain Maltol in addition to diethyl-.alpha.,.beta.-diacetyl succinate, while Formulas VC and VD contain only diethyl-.alpha.,.beta.-diacetyl succinate as a complete replacement for Maltol. The pineapple flavor achieved by the use of Formula VC is comparable if not superior to the flavor of Formula VA, while the flavor achieved by the use of Formula VD is comparable if not superior to the flavor of VB. The replacement proportion of Maltol by diethyl-.alpha.,.beta.-diacetyl succinate is approximately one part weight to one part by weight of the Maltol.
Example Vi
Wine Flavor Composition
The wine flavor composition is produced by initially adding 0.08 parts by weight of diethyl-.alpha.,.beta.-diacetyl succinate to 99.92 parts by weight of natural wine flavor. Four liquid ounces of the wine concentrate are added to one gallon of wine.
A wine flavor composition may also be produced by preparing a 1% by weight ethanol solution of diethyl-.alpha.,.beta.-diacetyl succinate and then adding 0.32 fluid ounces of the solution to 1 gallon of wine. This is equivalent to 25 parts per million.
Example Vii
Tobacco Flavor Composition
A 1% ethanol solution of diethyl-.alpha.,.beta.-diacetyl succinate is sprayed on smoking tobacco at the rate of 4 ounces of solution per 100 pounds of tobacco. After the alcohol is allowed to evaporate, a tobacco flavor composition results.
To produce a flavored tobacco which also contains synthetic tobacco, the procedure for the production of tobacco flavor composition heretofore described in this Example is repeated except that instead of employing smoking tobacco only, synthetic tobacco such as cellulose fibers, for example, the cellulose fibers sold by the Celanese Chemical Company under the trademark "CYTREL" or the cellulose fibers sold by Imperial Chemical Corporation under the trademark "POLYSTREP", is blended with the flavored tobacco in a ratio of approximately 1 to 1 by weight.
In a third procedure, a 1% ethanol solution of diethyl-.alpha.,.beta.-diacetyl succinate is sprayed on synthetic tobacco, such as cellulose fibers, at the rate of 4 ounces of solution of 100 pounds of synthetic tobacco. After the alcohol is allowed to evaporate, a tobacco flavor synthetic composition results.
Any one of the above tobacco flavor compositions may be used in cigarettes, producing a striking improvement in flavor.
For the treatment of tobacco, it is desirable that the flavor enhancer be in solubilized form, such as in an ethanol solution, as in the example of diethyl-.alpha.,.beta.-diacetyl succinate.
Example Viii
Carbonated Soft Drinks
A fruit flavor carbonated drink is produced by dissolving one ounce by weight of one of the flavor compositions such as described in Examples I or II in one gallon of sugar syrup. One ounce of the resulting mixture is added to about five ounces of carbonated water to produce six ounces of carbonated beverage. The flavor composition containing 2.5% by weight of diethyl-.alpha.,.beta.-diacetyl succinate results in a level of 32 parts per million of the diethyl-.alpha.,.beta.-diacetyl succinate flavor enhancer in the total carbonated drink produced.
In Examples I through IX, dimethyl-.alpha.,.beta.-diacetyl succinate may be utilized as the flavor enhancer in the same amounts indicated for diethyl-.alpha.,.beta.-diacetyl succinate used in those Examples.
Example Ix
Butterscotch Flavor Composition
Two butterscotch compositions each containing a different flavor enhancer in accordance with the teaching of the invention were prepared. For comparison, another composition containing the same ingredients but without either of the flavor enhancers used in A and B was also prepared as a control. The formulas of the compositions are as follows:
Each of the butterscotch compositions containing the flavor enhancers (A) and (B) had an immeasurably superior flavor over the control. The butterscotch compositions (A) and (B) had a better butterscotch caramel flavor and an increased sweetness and mouth feel. The butter notes were also enhanced.
Claims
What is claimed is:
1. A flavor composition comprising a flavor component and 0.0001% to 30% by weight of a dialkyl-.alpha.,.beta.-diacyl succinate having the formula: ##STR2## in which R.sub.1 is a straight or branched chain alkyl having less than 6 carbon atoms or cyclohexyl and R.sub.2 is a straight or branched chain alkyl having less than 7 carbon atoms or cyclohexyl, the organoleptic properties of said flavor component being enhanced by said succinate.
2. A flavor composition of claim 1 in which the dialkyl-.alpha.,.beta.-diacyl succinate is dimethyl-.alpha.,.beta.-diacetyl succinate.
3. A flavor composition of claim 1 in which the dialkyl-.alpha.,.beta.-diacyl succinate is diethyl-.alpha.,.beta.-diacetyl succinate.
4. A flavor composition of claim 1 in which the dialkyl-.alpha.,.beta.-diacyl succinate present is 0.001% to 20% by weight of the composition.
5. A flavor composition of claim 1 in which the dialkyl-.alpha.,.beta.-diacyl succinate present is 0.0025% to 5% by weight of the composition.
6. A flavor composition of claim 1 in which the dialkyl-.alpha.,.beta.-diacyl succinate is diethyl-.alpha.,.beta.-dipropionyl succinate.
7. A flavor composition of claim 1 in which the dialkyl-.alpha.,.beta.-diacyl succinate is dicyclohexyl-.alpha.,.beta.-diacetyl succinate.
Patent Citations (1)
| Patent | Date | Inventor | Cited By |
|---|---|---|---|
| US4140134 | 1979-02-01 | Willis et al. |