Participants
| Role | Name | HCID | Charge |
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| Reactant | Lactulose | HCID 11333 | — |
| Solvent | Water | HCID 962 | — |
| Product | Lactitol dihydrate | HCID 157354 | — |
| Product | Lactitol Monohydrate | HCID 3067270 | — |
Reaction Steps
Because the mixture according to the invention is a liquid, it is preferable to start from the lactitol reaction mixture obtained after the hydrogenation of lactose. Said reaction is usually performed in an aqueous medium in the presence of a suitable hydrogenation catalyst. The lactitol solution in water obtained after filtration, purification and possibly concentration by evaporation is very suitable as a source of lactitol for the preparation of the mixture according to the invention. The condition for using such a solution is, however, that the lactitol solution is sufficiently pure, that is to say at least 90% by weight, and preferably 95% by weight, of the content of dissolved solids is composed of lactitol. The advantage of using such a lactitol is that no crystallization step is necessary to obtain crystalline lactitol monohydrate or crystalline lactitol dihydrate which then has to be redissolved. The advantage of using a crystalline lactitol hydrate is the high purity (usually more than 97% by weight of lactitol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06444250B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-2a5e4ca8d1144f40a279578c97fc92b7 |
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| Source note | uspto-grants-2002_09 |
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