Title: Alternative Sweeteners

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High Fructose Corn Syrup 403 Table 8 HFCS Physical Constants Refractometer Specific Pounds Refractive index Brix 1966 gravity (in air) per U.S. gal. at Hydrometer Brix Solids % 20°C 45°C ICUMSA 20°C 20°C 20°C 42% HFCS 11.0 1.3493 1.3457 10.92 1.04414 8.689 10.99 70.5 1.4632 1.4577 69.10 1.34717 11.211 69.54 71.0 1.4643 1.4589 69.55 1.35022 11.236 70.02 71.5 1.4655 1.4600 70.04 1.35327 11.261 70.50 72.0 1.4667 1.4612 70.54 1.35633 11.287 70.99 55% HFCS 11.0 1.3492 1.3456 10.90 1.04418 8.689 11.00 76.5 1.4774 1.4716 74.84 1.38454 11.522 75.38 77.0 1.4786 1.4728 75.31 1.38769 11.548 75.87 77.5 1.4798 1.4740 75.78 1.39084 11.574 76.35 Source: Complied from CRA, ISBT, and ICUMSA. values can be mathematically converted between the two units and, for the convenience of those more familiar with RBU color, that conversion equation is as follows: RBU CRA 100 0.0417 0.0479 The most commonly tested attributes are dry solids and pH, probably because many quality control laboratories are equipped to perform these tests. Dry solids are determined by refractometer. Many refractometers are calibrated with the Brix scale rather than refractive index. For sucrose solutions, Brix corresponds to percent solids in solution. The term Brix cannot be used when designating solids concentrations in other nutritive sweetener solutions such as invert sugars, HFCS, and corn syrups (8). From Table 8 it can be seen that for HFCS products the refractive index-Brix relationship is not the same as the refractive indexsolids relationship. For 42% HFCS, the Brix value is roughly 1.4 less than the actual delivered solids, and for 55% HFCS, the difference is about 1.7. The difference is less at lower solids levels and at 10% solids the difference is only 0.1° Brix. Also, it is important to realize the effect of temperature on the converted dry solids value. There is a 0.1% solids error in the dry solids reading for every 1°C difference from 20°C. For example a refractive index or Brix reading taken at 25°C will result in a 77.0% solids value being reported as 76.5%.
404 Buck Because of the high purity of HFCS, it has low ionic strength and buffering capacity. For this reason it is imperative that pure dilution water be used and that residual buffer solutions be removed from the probes to prevent erroneous pH results. Although pH is the most commonly used test, titratable acidity is a better indicator of the effect HFCS may have on the pH of a food system. VI. PROPERTIES Functionally, HFCS provides sweetness, flavor enhancement, viscosity, humectancy, nutritive solids, fermentability, and reducing characteristics such as flavor and color development. HFCS can be used to control crystallization, modify freezing point, raise osmotic pressure, and lower water activity. By far, sweetness is the most important functional property of HFCS. Table 9 shows the relative sweetness of several sweeteners compared with sucrose. Although sweetness levels may be comparable, the actual sweetness may vary in a food system, depending on such factors as the temperature, pH, and solids. Sweetness is also affected by the flavor profile (9). HFCS has a rapid sweetness release. Compared with sucrose, HFCS is considered to enhance fruit flavors, spicy notes, and tartness. This is because the sweetness of HFCS is quickly perceived and does not linger. Sucrose on the other hand has a slower onset of sweetness but a longer lasting action. This can have a flavor-masking effect. The combination of the two can result in a synergism that results in a system perceived sweeter than the individual ingredients on their own. Over the shelf-life of a product, acidic food systems (such as most beverages) sweetened with sucrose will invert, changing the sugar profile and consequently the flavor and sweetness of the product. HFCS has an advantage over sucrose in acidic food systems because it does not invert. Table 10 illustrates the effect of sucrose inversion. Table 9 Relative Sweetness of Nutritive <strong>Sweeteners</strong> Sweetener Sweetness relative to sucrose Sucrose 1.0 Crystalline fructose 1.2–1.8 90% HFCS 1.2–1.6 42% HFCS 1.0 55% HFCS 1.0 Sucrose medium invert 1.0 Dextrose 0.7
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ISBN: 0-8247-0437-1 This book is pr
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iv Preface these sweeteners are bei
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vi Contents 7. Tagatose 105 Hans Be
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Contributors Sue E. Andress The Nut
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Contributors xi Carolyn M. Merkel M
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1 Alternative Sweeteners: An Overvi
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Overview 3 II. RELATIVE SWEETNESS P
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Overview 5 IV. INTERNATIONAL REGULA
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Overview 7 V. U.S. REGULATION OF SW
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Overview 9 General recognition of s
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Overview 11 the maximum dietary lev
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2 Acesulfame K Gert-Wolfhard von Ry
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Acesulfame K 15 Figure 3 Acesulfame
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Acesulfame K 17 Figure 4 Sweetness
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Acesulfame K 19 The acute oral toxi
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Acesulfame K 21 Table 2 Stability o
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Acesulfame K 23 were preferred over
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Acesulfame K 25 losses during bakin
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Acesulfame K 27 All methods describ
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Acesulfame K 29 24. Report of the S
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3 Alitame Michael H. Auerbach Danis
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Alitame 33 IV. SOLUBILITY At the is
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Alitame 35 Figure 3 Alitame and asp
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Alitame 37 Figure 5 Metabolism of a
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Alitame 39 autonomic, gastrointesti
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4 Aspartame Harriett H. Butchko, W.
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Aspartame 43 Figure 2 Principal con
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Aspartame 45 A wide range exists ov
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Aspartame 47 Figure 4 Dietary intak
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Aspartame 49 day for 60-kg adults (
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Aspartame 51 mood, and behavior (88
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Aspartame 53 VI. WORLDWIDE REGULATO
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Aspartame 55 30. A Bar, C Biermann.
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Aspartame 57 67. HH Butchko, C Tsch
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Aspartame 59 104. AF Stokes, A Belg
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Aspartame 61 144. D Squillacote. As
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64 Bopp and Price Figure 1 Structur
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66 Bopp and Price Table 1 Regulator
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68 Bopp and Price V. ADMIXTURE POTE
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70 Bopp and Price and thickeners (1
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72 Bopp and Price XII. METABOLISM C
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74 Bopp and Price sodium cyclamate
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76 Bopp and Price ied during the pa
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78 Bopp and Price the studies invol
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80 Bopp and Price 0.42 µg/ml and w
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82 Bopp and Price 4. U.S. Patent No
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84 Bopp and Price 48. SM Sieber, RH
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6 Neohesperidin Dihydrochalcone Fra
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Neohesperidin Dihydrochalcone 89 Fi
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Neohesperidin Dihydrochalcone 91 Fi
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Neohesperidin Dihydrochalcone 93 in
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Neohesperidin Dihydrochalcone 95 ot
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Neohesperidin Dihydrochalcone 97 Ta
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Neohesperidin Dihydrochalcone 99 th
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Neohesperidin Dihydrochalcone 101 c
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Neohesperidin Dihydrochalcone 103 5
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7 Tagatose Hans Bertelsen and Søre
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Tagatose 107 the same type of Food
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Tagatose 109 in pigs according to m
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Tagatose 111 IV. USE OF D-TAGATOSE
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Tagatose 113 rinsing periods or dur
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Tagatose 115 anaerobic bacterial fe
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Tagatose 117 The intestines of both
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Tagatose 119 Table 1 Relative Sweet
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Tagatose 121 D. Hygroscopicity Taga
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Tagatose 123 Table 2 Heat of Soluti
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Tagatose 125 In conclusion, tagatos
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Tagatose 127 24. BB Jensen, B Buema
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130 Stargel et al. Figure 1 Compari
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132 Stargel et al. Figure 2 Matrix
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134 Stargel et al. ness of neotame
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136 Stargel et al. Figure 4 Taste p
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138 Stargel et al. Table 1 Solubili
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140 Stargel et al. study strains in
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142 Stargel et al. to 10,000 µg/pl
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144 Stargel et al. for general use
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9 Saccharin Ronald L. Pearson PMC S
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Saccharin 149 proved for use in the
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Saccharin 151 was added to sodium d
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Saccharin 153 Table 2 Economics of
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Saccharin 155 Table 4 Saccharin Adm
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Table 6 Flavor Profile and Cost Com
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Saccharin 159 Figure 5 Hydrolysis o
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Saccharin 161 malian repellant (52,
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Saccharin 163 REFERENCES 1. GE DuBo
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Saccharin 165 67. GP Schoenig, et a
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168 Kinghorn et al. herbarium speci
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170 Kinghorn et al. Figure 1 Struct
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172 Kinghorn et al. V. USE AND ADMI
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174 Kinghorn et al. sulting in the
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176 Kinghorn et al. Figure 2 Struct
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178 Kinghorn et al. iol administere
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180 Kinghorn et al. cus mutans, or
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182 Kinghorn et al. a natural sweet
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11 Sucralose Leslie A. Goldsmith an
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Sucralose 187 Figure 2 Sweeteness i
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Sucralose 189 cant difference was f
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Sucralose 191 fructose, and/or insu
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Sucralose 193 Figure 4 Sucralose so
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Sucralose 195 Figure 6 Viscosities
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Sucralose 197 Table 2 Sucralose Int
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Sucralose 199 tively, compared with
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Sucralose 201 Figure 10 Breakdown o
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Sucralose 203 Table 3 Percent Mass
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Sucralose 205 Table 4 Initial Appli
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Sucralose 207 4. Sucralose Safety A
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210 Kinghorn and Compadre establish
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212 Kinghorn and Compadre grosvenor
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214 Kinghorn and Compadre form. Phy
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216 Kinghorn and Compadre of the de
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218 Kinghorn and Compadre Figure 5
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226 Kinghorn and Compadre sweet tas
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230 Kinghorn and Compadre 5. O Tana
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232 Kinghorn and Compadre 41. S Nir
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13 Erythritol Milda E. Embuscado an
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Erythritol 237 The commercial produ
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Table 2 Properties of Erythritol Co
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Erythritol 241 used to obtain the d
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Erythritol 243 crose stabilized and
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Erythritol 245 Figure 4 (A) Rate of
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Table 6 Assessment Criteria for the
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Table 7 Summary of Pivotal Toxicity
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Erythritol 251 VI. FOOD AND PHARMAC
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Erythritol 253 5. C Servo, J Pabo,
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14 Hydrogenated Starch Hydrolysates
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Figure 1 (a) Chemical structures fo
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Hydrogenated Starch Hydrolysates an
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15 Isomalt Marie-Christel Wijers* P
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Isomalt 267 GPM depends on the isom
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Isomalt 269 IV. PHYSICO-CHEMICAL PR
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Isomalt 271 temperature than sucros
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Isomalt 273 C. Diabetics A number o
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Isomalt 275 Figure 7 Changes in wei
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Isomalt 277 C. Chewing Gum Sticks,
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Isomalt 279 isomalt is significantl
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Isomalt 281 der Sorbit-Toleranz ges
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16 Maltitol Kazuaki Kato Towa Chemi
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Maltitol 285 Like the other polyols
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Maltitol 287 of shape over time), h
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Maltitol 289 results of this confer
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Maltitol 291 available on certain p
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Maltitol 293 Table 3 Worldwide Stat
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Maltitol 295 alcohol. Unpublished r
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298 Mesters et al. Figure 1 The che
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300 Mesters et al. rium and equal m
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302 Mesters et al. sugars are then
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304 Mesters et al. Figure 2 Telemet
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306 Mesters et al. Figure 3 Moistur
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308 Mesters et al. Figure 6 Viscosi
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310 Mesters et al. tose are the mai
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312 Mesters et al. Figure 8 The wat
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314 Mesters et al. food containing
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18 Sorbitol and Mannitol Anh S. Le
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Sorbitol and Mannitol 319 Figure 2
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Table 1 Physical Properties of the
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Sorbitol and Mannitol 323 Figure 4
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Sorbitol and Mannitol 325 bases are
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Sorbitol and Mannitol 327 is used a
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Sorbitol and Mannitol 329 ‘‘cap
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Sorbitol and Mannitol 331 that mann
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Sorbitol and Mannitol 333 Mannitol
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19 Xylitol Philip M. Olinger Polyol
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Xylitol 337 Milled forms of xylitol
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Xylitol 339 Table 2 Solubility of S
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Xylitol 341 tol in a fluoride tooth
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Xylitol 343 The recognition of xyli
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Xylitol 345 tion of the availabilit
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Xylitol 347 grow and metabolize opt
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Xylitol 349 VIII. USE OF XYLITOL AS
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Xylitol 351 IX. USE OF XYLITOL IN P
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Page 370 and 371: Xylitol 357 71. JDB Featherstone, T
Page 372 and 373: Xylitol 359 112. JS Van der Hoeven.
Page 374 and 375: Xylitol 361 tans omz 176 by xylitol
Page 376 and 377: Xylitol 363 BL Horecker, K Lang, Y
Page 378: Xylitol 365 of Certain Food Additiv
Page 381 and 382: 368 White and Osberger II. MANUFACT
Page 383 and 384: 370 White and Osberger scribe impro
Page 385 and 386: 372 White and Osberger Figure 1 Cyc
Page 387 and 388: 374 White and Osberger When asparta
Page 389 and 390: 376 White and Osberger Table 5 Temp
Page 391 and 392: 378 White and Osberger Figure 3 Met
Page 393 and 394: 380 White and Osberger Figure 5 Com
Page 395 and 396: 382 White and Osberger Table 6 Glyc
Page 397 and 398: 384 White and Osberger Table 8 Low-
Page 399 and 400: 386 White and Osberger F. Confectio
Page 401 and 402: 388 White and Osberger In 1993, Vui
Page 403 and 404: 390 White and Osberger 18. AL Forbe
Page 405 and 406: 392 Buck Table 1 Market Division be
Page 407 and 408: 394 Buck Table 3 World HFS Consumpt
Page 409 and 410: 396 Buck Figure 3 Production of 42%
Page 411 and 412: 398 Buck Table 4 Typical Characteri
Page 413 and 414: 400 Buck Table 5 Effect of Temperat
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Page 419 and 420: 406 Buck VII. APPLICATIONS HFCS rep
Page 421 and 422: 408 Buck is a benefit and in other
Page 423 and 424: 410 Buck 1986. This evaluation conc
Page 426 and 427: 22 Isomaltulose William E. Irwin* P
Page 428 and 429: Isomaltulose 415 Figure 2 Isosweet
Page 430 and 431: Isomaltulose 417 Figure 3 Solubilit
Page 432 and 433: Isomaltulose 419 Figure 6 Plasma in
Page 434: Isomaltulose 421 6. Dreissig VW, Lu
Page 437 and 438: 424 Richards and Dexter various pla
Page 439 and 440: 426 Richards and Dexter from assays
Page 441 and 442: 428 Richards and Dexter desiccation
Page 443 and 444: 430 Richards and Dexter 2. Taste Qu
Page 445 and 446: 432 Richards and Dexter parative da
Page 447 and 448: 434 Richards and Dexter Table 3 Com
Page 449 and 450: 436 Richards and Dexter dissipate t
Page 451 and 452: 438 Richards and Dexter unpublished
Page 453 and 454: 440 Richards and Dexter IX. SHELF-L
Page 455 and 456: Figure 7 Egg white (95 g) was mixed
Page 457 and 458: 444 Richards and Dexter Figure 10 B
Page 459 and 460: 446 Richards and Dexter Figure 12 O
Page 461 and 462: 448 Richards and Dexter Figure 14 T
Page 463 and 464: 450 Richards and Dexter XIII. CARIO
Page 465 and 466: 452 Richards and Dexter tions was s
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454 Richards and Dexter activity, a
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456 Richards and Dexter E. 14-day T
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458 Richards and Dexter 3. J Leibow
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460 Richards and Dexter 41. LM Crow
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24 Mixed Sweetener Functionality Ab
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Mixed Sweetener Functionality 465 2
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Mixed Sweetener Functionality 467 T
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Mixed Sweetener Functionality 471 F
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Mixed Sweetener Functionality 479 I
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25 Aspartame-Acesulfame: Twinsweet
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Aspartame-Acesulfame: Twinsweet 483
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26 Polydextrose Helen Mitchell Dani
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Polydextrose 501 Table 1 Approximat
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Polydextrose 503 at 25°C. Polydext
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Polydextrose 505 Figure 4 Hygroscop
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Polydextrose 507 Table 5 Functional
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Polydextrose 509 F. Fiber Polydextr
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Polydextrose 511 providing bulk, mo
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Polydextrose 513 H. Soft Candy The
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Polydextrose 515 B. International T
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Polydextrose 517 chemical and econo
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520 Deis I. FAT IS ESSENTIAL AND FU
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522 Deis Figure 1 Ingredient suppor
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524 Deis binding water, thus provid
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526 Deis The U.S. Department of Agr
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528 Deis stabilizer, thickener, or
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530 Deis mouth feel and rate of gel
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532 Deis Figure 4 Structure of glyc
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534 Deis Table 4 General Categories
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536 Deis ninths of the fat availabl
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538 Deis the same function in all f
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540 Deis 28. Anon. Glycerine: like
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542 Index [Alitame] solubility, 33
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544 Index [Erythritol] gastrointest
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546 Index [High fructose corn syrup
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548 Index Mogrosides, 211-213 prope
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550 Index [Polyols] isomalt, 265-28
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552 Index [Sucralose] safety, 189-1
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