In the manipulation twenty-five cubic centimeters each of the copper and alkali solutions are mixed and boiled and an equal volume of the maltose solution added, which should not contain more than one per cent of the sugar. The boiling is continued for four minutes, an equal volume of cold recently boiled water added, the cuprous oxid separated by filtration and the metallic copper obtained in the manner already described. The weight of maltose oxidized is then ascertained from the table.

Table for Maltose.

(A) (B) (A) (B) (A) (B) (A) (B)
 30  25.3 35  29.6 40  33.9 45  38.3
 31  26.1 36  30.5 41  34.8 46  39.1
 32  27.0 37  31.3 42  35.7 47  40.0
 33  27.9 38  32.2 43  36.5 48  40.9
 34  28.7 39  33.1 44  37.4 49  41.8
(A) (B) (A) (B) (A) (B) (A) (B)
 50  42.6 94  81.2138 120.6182 160.1
 51  43.5 95  82.1139 121.5183 160.9
 52  44.4 96  83.0140 122.4184 161.8
 53  45.2 97  83.9141 123.3185 162.7
 54  46.1 98  84.8142 124.2186 163.6
 55  47.0 99  85.7143 125.1187 164.5
 56  47.8100  86.6144 126.0188 165.4
 57  48.7101  87.5145 126.9189 166.3
 58  49.6102  88.4146 127.8190 167.2
 59  50.4103  89.2147 128.7191 168.1
 60  51.3104  90.1148 129.6 192 169.0
 61  52.2105  91.0149 130.5193 169.8
 62  53.1106  91.9150 131.4194 170.7
 63  53.9107  92.8151 132.3195 171.6
 64  54.8108  93.7152 133.2196 172.5
 65  55.7109  94.6153 134.1197 173.4
 66  56.6110  95.5154 135.0198 174.3
 67  57.4111  96.4155 135.9199 175.2
 68  58.3112  97.3156 136.8200 176.1
 69  59.2113  98.1157 137.7201 177.0
 70  60.1114  99.0158 138.6202 177.9
 71  61.0115  99.9159 139.5203 178.7
 72  61.8116 100.8160 140.4204 179.6
 73  62.7117 101.7161 141.3205 180.5
 74  63.6118 102.6162 142.2206 181.4
 75  64.5119 103.5163 143.1207 182.3
 76  65.4120 104.4164 144.0208 183.2
 77  66.2121 105.3165 144.9209 184.1
 78  67.1122 106.2166 145.8210 185.0
 79  68.0123 107.1167 146.7211 185.9
 80  68.9124 108.0168 147.6212 186.8
 81  69.7125 108.9169 148.5213 187.7
 82  70.6126 109.8170 149.4214 188.6
 83  71.5127 110.7171 150.3215 189.5
 84  72.4128 111.6172 151.2216 190.4
 85  73.2129 112.5173 152.0217 191.2
 86  74.1130 113.4174 152.9218 192.1
 87  75.0131 114.3175 153.8219 193.0
 88  75.9132 115.2176 154.7220 193.9
 89  76.8133 116.1177 155.6221 194.8
 90  77.7134 117.0178 156.5222 195.7
 91  78.6135 117.9179 157.4223 196.6
 92  79.5136 118.8180 158.3224 197.5
 93  80.3137 119.7181 159.2225 198.4
(A) (B) (A) (B) (A) (B) (A) (B)
226 199.3245 216.3264 233.4283 250.4
227 200.2246 217.2265 234.3284 251.3
228 201.1247 218.1266 235.2285 252.2
229 202.0248 219.0267 236.1286 253.1
230 202.9249 219.9268 237.0287 254.0
231 203.8250 220.8269 237.9288 254.9
232 204.7251 221.7270 238.8289 255.8
233 205.6252 222.6271 239.7290 256.6
234 206.5253 223.5272 240.6291 257.5
235 207.4254 224.4273 241.5292 258.4
236 208.3255 225.3274 242.4293 259.3
237 209.1256 226.2275 243.3294 260.2
238 210.0257 227.1276 244.2295 261.1
239 210.9258 228.0277 245.1296 262.0
240 211.8259 228.9278 246.0297 262.8
241 212.7260 229.8279 246.9298 263.7
242 213.6261 230.7280 247.8299 264.6
243 214.5262 231.6281 248.7300 265.5
244 215.4263 232.5282 249.6

145. Preparation of Levulose.—It is not often that levulose, unmixed with other reducing sugars, is brought to the attention of the analyst. It probably does not exist in the unmixed state in any agricultural product. The easiest method of preparing it is by the hydrolysis of inulin. A nearly pure levulose has also lately been placed on the market under the name of diabetin. It is prepared from invert sugar.

Inulin is prepared from dahlia bulbs by boiling the pulp with water and a trace of calcium carbonate. The extract is concentrated to a sirup and subjected to a freezing temperature to promote the crystallization of the inulin. The separated product is subjected to the above operations several times until it is pure and colorless. It is then washed with alcohol and ether and is reduced to a fine powder. Before the repeated treatment with water it is advisable to clarify the solution with lead subacetate. The lead is afterwards removed by hydrogen sulfid and the resultant acetic acid neutralized with calcium carbonate.

By the action of hot dilute acids inulin is rapidly converted into levulose.

Levulose may also be prepared from invert sugar, but in this case it is difficult to free it from traces of dextrose. The most successful method consists in forming a lime compound with the invert sugar and separating the lime levulosate and dextrosate by their difference in solubility. The levulose salt is much less soluble than the corresponding compound of dextrose. In the manufacture of levulose from beet molasses, the latter is dissolved in six times its weight of water and inverted with a quantity of hydrochloric acid, proportioned to the quantity of ash present in the sample. After inversion the mixture is cooled to zero and the levulose precipitated by adding fine-ground lime. The dextrose and coloring matters in these conditions are not thrown down. The precipitated lime levulosate is separated by filtration and washed with ice-cold water. The lime salt is afterwards beaten to a cream with water and decomposed by carbon dioxid. The levulose, after filtration, is concentrated to the crystallizing point.[110]

146. Estimation of Levulose.—Levulose, when free of any admixture with other reducing sugars, may be determined by the copper method with the use of the subjoined table, prepared by Lehmann.[111] The copper solution is the same as that used for invert sugar, viz., 69.278 grams of pure copper sulfate in one liter. The alkali solution is prepared by dissolving 346 grams of rochelle salt and 250 grams of sodium hydroxid in water and completing the volume to one liter.