Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | L-Lysine | HCID 5962 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | L-Lysine, acetate (1:1) | HCID 104152 | — |
Reaction Steps
To the above effluent solution obtained by the method of Example 2, acetic acid was added so as to become 1.0 molar equivalent with L-lysine, and decolored by activated carbon, followed by filtration. The filtrate was concentrated to 95 g/dL L-lysine under reduced pressure, cooled to 15° C., and crystals were separated by centrifugation. The resulting crystals ware washed with 100% methanol, and dried under reduced pressure to obtain L-lysine acetic acid salt product. The recovery of the product from the feed solution (yield of L-lysine) was 57.6%. The purity of the product was examined according to the method described in Japanese Pharmacopoeia, 16th Revision (pp 1385-1386), and found to be 100%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09216946B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-fba20f3cd686435887f6b056e20a56ee |
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| Source note | uspto-grants-2015_12 |
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