1. Field of the Invention
This invention relates to enhanced flavoring compositions containing N-ethyl-p-menthane-3-carboxamide, confectionery compositions and chewing gums containing the enhanced flavoring compositions and methods of making the same.
2. Description of the Prior Art
Much work has been done in the food arts to enhance the impact of the flavors used in confectionery products and chewing gums. Flavor ingredients for use in these end products have been coated, encapsulated, combined with other active and inactive ingredients, and the like. U.S. Pat. Nos. 3,857,964, 3,897,566, 3,930,026, 4,388,328, 4,485,118, 4,568,560, 4,590,075, 4,752,481, 4,803,082, 5,004,595, 5,041,294, 5,266,335 and 5,284,659 all concern aspects of flavor modification.
Much of the effort was directed toward control of flavor release in the end product, particularly in gum products. The release of the flavor from a food product is largely determined by the matrix of the food product. Gum products, having a matrix composed of an elastomeric gum base, corn syrup and sweetener, withhold flavor, usually at 60-75% of the amount of flavor used, the percentage depending somewhat on the flavor's affinity for the matrix. Higher amounts of flavors are therefore used in gums in order to provide a perceptible flavor effect.
Particular attention has been paid to enhancing the impact of fruit flavors in chewing gums. Because of their chemical makeup, fruit flavors have a particularly high affinity for gum base. Fruit flavors also have a light flavor quality which provides for a low flavor impact. U.S. Pat. No. 5,158,790, for example, teaches the use of L-carvone with fruit flavors to overcome these deficits and enhance sweetness and flavor. U.S. Pat. Nos. 5,415,888 and 5,429,827 teach the use of a polymer restrainer having a particular solubility parameter relative to the fruit flavor to control release.
The synergistic effects provided by the use of substances as flavor enhancers is also well known in the food arts. Synergism in flavoring is the addition of very small amounts of a non-specific material to accentuate the specific flavoring material. Known synergisms include for example, the use of citric acid in peppermint to accentuate the peppermint, vanilla in chocolate to accentuate the chocolate flavor, oil of lemon in molasses, oil of peppermint in licorice or anise, and the use of salt in most candies except butter flavored candies.
Cooling agents are compounds used in confectionery compositions and chewing gums for their cooling sensation and breath freshening effects with or without the presence of flavoring agents. Menthol is perhaps the best known cooling agent but one with well-known drawbacks such as high volatility, bitterness and a strong minty flavor. N-ethyl-p-menthane-3-carboxamide is also known as a cooling agent. U.S. Pat. No. 4,193,936 teaches N-ethyl-p-menthane-3-carboxamide as being less volatile than menthol and having little or no odor. U.S. Pat. Nos. 4,060,091, 4,136,163, and 5,405,604 teach the use of N-ethyl-p-menthane-3-carboxamide as a cooling agent in edible compositions. U.S. Pat. No. 5,009,893, U.S. Pat. No. 5,244,670, WO 93/23005 and WO 93/25177 all disclose use of N-ethyl-p-menthane-3-carboxamide as an adjuvant with other cooling agents including menthol. WO 97/06695 teaches however that compounds used as cooling agents all have a negative impact on flavors, particularly fruit flavors. WO 97/06695 further teaches that in order to avoid the problem, flavors and cooling agents must be formulated into distinct and discreet regions of the confectionery product.
Thus it is known to use N-ethyl-p-menthane-3-carboxamide to provide cooling effects and enhancement of breath freshening effects, particularly in mint-flavored gum and confectionery products. The food arts however do not teach the use of N-ethyl-p-menthane-3-carboxamide as a flavor enhancer. More specifically, the art does not teach the use of N-ethyl-p-menthane-3-carboxamide in combination with flavors, particularly in combination with fruit flavors, in gum and confectionery products, at levels which produce synergistic effects.
The present invention provides an enhanced flavoring composition comprising at least one flavoring agent and an amount of N-ethyl-p-menthane-3-carboxamide effective to enhance the flavoring agent wherein the N-ethyl-p-menthane-3-carboxamide is present at about 0.04 to about 2.2% by weight of the enhanced flavoring composition. The invention further concerns a method for enhancing a flavoring agent which comprises adding thereto an effective amount of N-ethyl-p-menthane-3-carboxamide at about 0.04 to about 2.2% by weight of the combination. The invention further concerns chewing gums and confectionery compositions containing a flavoring effective amount of the enhanced flavoring compositions.
It has now surprisingly been found that N-ethyl-p-menthane-3-carboxamide can be used per se, as a flavor modifier to enhance the flavor of a flavoring agent. This synergistic effect is found when N-ethyl-p-menthane-3-carboxamide is used at low levels in combination with the flavoring agent. The character of the flavor is generally found to be sharper or brighter, punctuated, more defined and longer-lasting when compared with compositions containing the same flavoring agent without N-ethyl-p-menthane-3-carboxamide. The enhanced flavoring composition provides a long lasting flavor sensation to food compositions such as gums and confections, particularly to fruit flavored chewing gums.
The term “flavor” is used herein to mean the sensation produced by a material taken in the mouth, perceived principally by the senses of taste and smell. Flavor is also taken to mean the sum of the characteristics of the material which produces that sensation. The term “flavoring agent” is used herein to mean the composition of natural or synthetic oils which produces the flavor sensation. Flavoring agents are well known in the confectionery arts.
Flavors contemplated herein include but are not limited to fruit flavors such as berry, citrus, tropical fruit flavors and the like; herbal such as cinnamon, anise, coriander, eucalyptus, ginseng, fennel and the like; sweet such as honey, caramel, toffee, molasses and the like; and spice such as nutmeg, pepper, cinnamon, caramon, ginger, clove and the like. Other flavors known to those skilled in the art may also be enhanced by the use of low levels of N-ethyl-p-menthane-3-carboxamide.
The enhancement and perceived prolongation of fruit flavors is a preferred application of the present invention. Fruit flavors may be natural or synthetically produced and typically contain a combination of aromatic hydrocarbons such as esters, aldehydes and ketones, essential oils from plant materials such as orange oil, lemon oil or other natural oils, and distillates from botanical ingredients. Fruit flavors include but are not limited to, lemon, orange, lime, apricot, grapefruit, banana, cherry, apple, pineapple, grape, strawberry and blends such as tutti fruitti and fruit punch and the like.
The amounts of the flavoring agent and the N-ethyl-p-menthane-3-carboxamide in the enhanced flavoring composition will be from about 99.96% to about 97.8% of flavoring agent and about 0.04% to about 2.2% of N-ethyl-p-menthane-3-carboxamide, with 0.4% to 1.0% of N-ethyl-p-menthane-3-carboxamide being preferred. The amounts will depend somewhat on such factors as the flavor type, the end use and the effect desired.
The amount of the enhanced flavoring composition to be used in the end product will also be dependent on the flavor type, the end product and the effect desired. In general the enhanced flavoring composition may suitably be used in confectionery compositions in a range of about 0.10% to about 1.0% by weight of the confection with 0.2% to 0.5% preferred. For chewing gums a higher range of about 0.8 to about 3.5% is suitable with 1.0% to 3.0% preferred.
The enhanced flavoring compositions of the present invention may be used in edible products such as hard and soft confections, and chewing gums. The preparation of confectionery formulations is historically well known and has changed little through the years. In general a hard boiled candy confection has a base composed of a mixture of sugar and other carbohydrate bulking agents kept in an amorphous or glassy condition, preferably having from about 0.5% to about 5% moisture. The base normally contains up to about 75% sugar (sucrose) and up to 65% corn syrup, with a higher sucrose to corn syrup ratio. Further ingredients such as flavoring agents, sweetening agents, acidulants, colorants and so forth may also be added. Hard boiled candies may also be prepared from non-fermentable sugars such as sorbitol, mannitol, xylitol, maltitol, erythritol, hydrogenated starch hydrolysates and the like.
Such confectionery may be routinely prepared by conventional methods such as those involving fire cookers, vacuum cookers, and scraped-surface cookers also referred to as high speed atmospheric cookers. Once the candy mass has been properly tempered, it may be cut into workable portions or formed into desired shapes. A variety of forming techniques may be utilized depending upon the shape and size of the final product desired. A general discussion of the composition and preparation of hard confections may be found in E. B. Jackson, Ed. “Sugar Confectionery Manufacture”, 2nd edition, Blackie Academic & Professional Press, Glasgow UK, (1990), at pages 129-169.
Similar to hard candy confection, soft candy confection may be utilize this invention. Soft candy includes fondants, caramels toffees, fudge, marshmallows and nougats and the like and may also include jams and jellies. The preparation of soft confections, such as nougat, involves conventional methods, such as the combination of two primary components, namely (1) a high boiling syrup such as a corn syrup, or the like, and (2) a relatively light textured frappe, generally prepared from egg albumin, gelatin, vegetable proteins, such as soy derived compounds, milk derived compounds such as milk proteins, and mixtures thereof. Further ingredients such as the enhanced flavoring agent, flavoring agents, additional carbohydrate bulking agent, colorants, preservatives, medicaments, mixtures thereof and the like may be added thereafter also under agitation. A general discussion of the composition and preparation of such confections may be found in E. B. Jackson, Ed. “Sugar Confectionery Manufacture”, 2nd edition, Blackie Academic & Professional Press, Glasgow UK, (1990), at pages 170-235.
Compressed tablet confections and lozenges are also within the scope of edible confectionery compositions of the present invention. Compressed tablet confections contain particular materials and are formed into structures under pressure. These confections generally contain sugars or sugar substitutes in amounts up to about 95%, by weight of the composition, and typical tablet excipients such as binders and lubricants as well as the enhanced flavoring agent, flavoring agents, colorants and so forth. Lozenges are cut from a sheet of firm dough and dried to give a hard sweet with a rough surface. A general discussion of the composition and preparation of such confections may be found in E. B. Jackson, Ed. “Sugar Confectionery Manufacture”, 2nd edition, Blackie Academic & Professional Press, Glasgow UK, (1990), at pages 236-258.
The enhanced flavoring compositions may likewise be used in chewing gums. The chewing gum composition generally comprises one or more natural or synthetic elastomer which is supplemented by conventional chewing gum ingredients. These ingredients include one or more solvents, plasticizers, fillers, flavoring agents, coloring agents and/or sweetening agents.
Elastomers which are suitable for use herein include substances of vegetable origin such as chicle, jelutong, gutta percha, guayale and crown gum. Synthetic elastomers such as butadiene-styrene copolymers, isobutylene-isoprene copolymers, polyethylene, polyisobutylene, polyvinylacetate, and mixtures thereof are also useful. The elastomer generally comprises from about 14% to 50% by weight, preferably from about 20% to about 30% by weight, of the chewing gum composition.
The chewing gum composition can contain elastomer solvents to aid in softening the polymer component. Such elastomer solvents can include methyl, glycerol or pentaerythritol esters of rosins or modified rosins, such as hydrogenated, dimerized or polymerized rosins or mixtures thereof. Examples of elastomer solvents suitable for use herein include pentaerythritol ester of partially hydrogenated wood rosin, pentaerythritol ester of wood rosin, glycerol ester of partially dimerized rosin, gylcerol ester of polymerized rosin, glycerol ester of tall oil rosin, glycerol ester of wood rosin, and partially hydrogenated wood rosin, and partially hydrogenated methyl ester of rosin, and mixtures thereof. Terpene resins, including polyterpene and mixtures thereof are also useful. The solvent can be employed in an amount ranging from about 10% to 75% and preferably about 15% to about 50% by weight of the chewing gum composition.
A variety of traditional ingredients used as plasticizers or emulsifiers such as lanolin, lecithin, glycerol monostearate, stearic acid, sodium stearate, potassium stearate, glycerol triacetate, triacetin, glycerine and the like can also be incorporated into the chewing gum composition to obtain a variety of textures and consistency properties. These additional materials also include waxes such as natural waxes, petroleum waxes and microcrystalline waxes and fats and oils including animal fats such as lard and tallow, vegetable oils such as soybean and cottonseed oil, hydrogenated and partially hydrogenated vegetable oil and cocoa butter. These ingredients are generally employed in amounts of up to about 30% by weight, preferably 1% to 25% by weight and more preferably from about 3% to about 7% by weight of the final chewing gum composition.
The chewing gum composition can additionally include conventional coloring agents such as titanium dioxide, in amounts up to 2% and fillers such as dicalcium phosphate, magnesium carbonate, aluminum hydroxide, alumina, aluminum silicates, talc, calcium carbonate, cellulose, and combinations thereof in amounts of from 5 to 35% by weight of the final composition.
The chewing gum composition may also contain bulk sweeteners including sugars such as sucrose, dextrose, maltose, fructose and the like or sugar alcohols such as sorbitol, mannitol, xylitol, maltitol, isomalt, erythritol and hydrogenated starch hydrolysates and combinations thereof. Bulk sweeteners may be present in amounts up to 90% by weight of the final composition. High intensity sweeteners such as aspartame, acesulfame salts, aliatame saccharin and the like may also be present. These sweeteners may be present in amounts of up to 1% by weight of the final gum composition.
The chewing gum may contain flavoring agents in addition to the enhanced flavoring compositions in amounts up to 3.5%. Generally any food additive such as those described in “Chemicals Used In Food Processing”, publication 1274, pages 63-258, by the National Academy of Sciences, may be used.
The chewing gum is generally manufactured by methods known in the art by sequentially adding the various chewing gum components to any commercial mixer or extruder in a batch or continuous process. The enhanced flavoring composition of the present invention is added to the chewing gum in the usual manner. After the ingredients have been thoroughly mixed the mass is discharged and cut, rolled, or shaped into the desired form.
The invention is illustrated by the following non-limiting examples.
N-ethyl-p-menthane-carboxamide available as “WS-3” supplied by Sterling Organics was used in the Examples.
A candy base (478.55 gms) was prepared by mixing a 55/45 ratio of granulated sugar and corn syrup with 47.9 gms of water and cooking the mixture to 145° C. The cooked base was transferred to a cooling table and 21.25 gms of a flavor premix was kneaded into the base while cooling. The flavored candy was formed by rolling through a drop roller. The flavor premix consisted of 20.0 gms salvage, and 1.25 gms flavor for a 0.25% by weight of flavor in the candy.
To a similarly prepared candy base (478.55 gms) was added 21.45 gms of second flavor premix also containing 20.0 gms salvage, and 1.25 gms flavor, with the addition of 0.20 gms of a 5% ethanol solution of N-ethyl-p-menthane-carboxamide (0.01 gms) for a 0.002% by weight of N-ethyl-p-menthane-carboxamide in the candy, and a flavor to N-ethyl-p-menthane-carboxamide ratio of 99.2 to 0.8.
Honey, citrus spice, herbal and apple flavored candies were prepared by the above methods both with and without the N-ethyl-p-menthane-carboxamide in the flavor premix. The four flavor pairs were evaluated as follows:
Nine people, randomly selected, were asked to evaluate the candies compounded with N-ethyl-p-menthane-carboxamide compared with the base candy without the additive. The evaluators were asked if the candy pairs “tasted different”. The following shows the number of people finding a different taste for the candy flavored as indicated: Citrus spice—6; apple—5; honey—5; herbal—5.
A. Preparation
1. A citrus flavored chewing gum was prepared by conventional means from 22.0 gms gum base, 69.04 gms sweetener, 0.24 gms high intensity sweetener, 2.97 gms acidulant, 3.85 gms other conventional additives and 1.9 gms citrus flavoring agent. Two additional samples were prepared in which 0.02 gms and 0.04 gms respectively of the sweetener were replaced with the same amount of N-ethyl-p-menthane-carboxamide for a flavor to N-ethyl-p-menthane-carboxamide ratio of 98.96/1.04 and 97.94/2.06 respectively. The control and the two inventive examples were compared as described further below.
2. A cinnamon flavored chewing gum was prepared by conventional means from 22.0 gms gum base, 73.29 gms sweetener, 0.81 gms high intensity sweetener, 2.1 gms other conventional additives and 1.8 gms cinnamon flavoring agent. Two additional samples were prepared in which 0.02 gms and 0.04 gms respectively of the sweetener were replaced with the same amount of N-ethyl-p-menthane-carboxamide for a flavor to N-ethyl-p-menthane-carboxamide ratio of 98.90/1.10 and 97.83/2.17 respectively. The control and the two inventive examples were compared as described further below.
B. Comparisons:
At a N-ethyl-p-menthane-carboxamide usage level of 0.02% the release of N-ethyl-p-menthane-carboxamide was expected to be about 50 ppm and at 0.04% usage level the release was expected to be about 100 ppm. The flavor enhanced gum products were compared with the corresponding control samples by a panel of six people who were asked to evaluate the samples by commenting on perceived flavor differences and flavor liking. Four of the six panelists noted differences in the samples summarized as follows:
For both the citrus and the cinnamon flavors, 0.02 gms of N-ethyl-p-menthane-carboxamide provided a preferred enhancement of the flavors. At 0.04 gms, while the flavors were enhanced, less desirable notes were also perceived.
Number | Name | Date | Kind |
---|---|---|---|
3857964 | Yolles | Dec 1974 | A |
3897566 | Bahoshy et al. | Jul 1975 | A |
3930026 | Clark | Dec 1975 | A |
4032661 | Rowsell et al. | Jun 1977 | A |
4060091 | Watson et al. | Nov 1977 | A |
4136163 | Watson et al. | Jan 1979 | A |
4193936 | Watson et al. | Mar 1980 | A |
4230688 | Rowsell et al. | Oct 1980 | A |
4271197 | Hopkins et al. | Jun 1981 | A |
4352822 | Cherukuri et al. | Oct 1982 | A |
4388328 | Glass | Jun 1983 | A |
4459425 | Amano et al. | Jul 1984 | A |
4485118 | Carroll et al. | Nov 1984 | A |
4497832 | Cherukuri et al. | Feb 1985 | A |
4568560 | Schobel | Feb 1986 | A |
4590075 | Wei et al. | May 1986 | A |
4751095 | Karl et al. | Jun 1988 | A |
4752481 | Dokuzovic | Jun 1988 | A |
4803082 | Cherukuri et al. | Feb 1989 | A |
4918182 | Jackson et al. | Apr 1990 | A |
4927646 | Jenner et al. | May 1990 | A |
4929447 | Yang | May 1990 | A |
4933190 | Cherukuri et al. | Jun 1990 | A |
4971797 | Cherukuri et al. | Nov 1990 | A |
4981698 | Cherukuri et al. | Jan 1991 | A |
5004595 | Cherukuri et al. | Apr 1991 | A |
5009893 | Cherukuri et al. | Apr 1991 | A |
5009900 | Levine et al. | Apr 1991 | A |
5041294 | Patel | Aug 1991 | A |
5158790 | Witkewitz et al. | Oct 1992 | A |
5244670 | Upson et al. | Sep 1993 | A |
5266335 | Cherukuri et al. | Nov 1993 | A |
5266592 | Grub et al. | Nov 1993 | A |
5284659 | Cherukuri et al. | Feb 1994 | A |
5372824 | Record et al. | Dec 1994 | A |
5405604 | Hall et al. | Apr 1995 | A |
5407665 | McLaughlin et al. | Apr 1995 | A |
5415880 | Song et al. | May 1995 | A |
5429827 | Song et al. | Jul 1995 | A |
5458879 | Singh et al. | Oct 1995 | A |
5545424 | Nakatsu et al. | Aug 1996 | A |
5603971 | Porzio et al. | Feb 1997 | A |
5633027 | Cherukuri et al. | May 1997 | A |
5725865 | Mane et al. | Mar 1998 | A |
5744180 | Cherukuri et al. | Apr 1998 | A |
5783725 | Kuhn et al. | Jul 1998 | A |
5800848 | Yatka et al. | Sep 1998 | A |
6159509 | Johnson et al. | Dec 2000 | A |
6306429 | Bealin-Kelly | Oct 2001 | B1 |
6379652 | Liu et al. | Apr 2002 | B1 |
6623266 | Jani et al. | Sep 2003 | B2 |
6627233 | Wolf et al. | Sep 2003 | B1 |
6673844 | Kumamoto et al. | Jan 2004 | B2 |
6780443 | Nakatsu et al. | Aug 2004 | B1 |
20020044968 | Van Lengerich | Apr 2002 | A1 |
20020119231 | Kumamoto et al. | Aug 2002 | A1 |
20020150616 | Vandecruys | Oct 2002 | A1 |
20030215532 | Nakatsu et al. | Nov 2003 | A1 |
20040238993 | Benczedi et al. | Dec 2004 | A1 |
20050019445 | Wolf et al. | Jan 2005 | A1 |
20050196517 | Hodanko et al. | Sep 2005 | A1 |
Number | Date | Country |
---|---|---|
0255260 | Feb 1988 | EP |
0434321 | Jun 1991 | EP |
452273 | Oct 1991 | EP |
0453397 | Oct 1991 | EP |
888067 | Jan 1999 | EP |
1003475 | May 2000 | EP |
1121927 | Aug 2001 | EP |
1215258 | Jun 2002 | EP |
1351761 | May 1974 | GB |
01206969 | Aug 1989 | JP |
8503414 | Aug 1985 | WO |
9004926 | May 1990 | WO |
9202145 | Feb 1992 | WO |
9323005 | Nov 1993 | WO |
9325177 | Dec 1993 | WO |
9507683 | Mar 1995 | WO |
9511671 | May 1995 | WO |
9603109 | Feb 1996 | WO |
9617524 | Jun 1996 | WO |
9702273 | Jan 1997 | WO |
9706695 | Feb 1997 | WO |
9803076 | Jan 1998 | WO |
9852540 | May 1998 | WO |
9847483 | Oct 1998 | WO |
9852545 | Nov 1998 | WO |
9913870 | Mar 1999 | WO |
0200039 | Jan 2002 | WO |
03063604 | Aug 2003 | WO |
03106404 | Dec 2003 | WO |
2004006967 | Jan 2004 | WO |
2004064544 | Aug 2004 | WO |
2005-082154 | Sep 2005 | WO |
2006003349 | Jan 2006 | WO |
2006039945 | Apr 2006 | WO |