Sialic acid analogs
US-9221858-B2 · Dec 29, 2015 · US
US10072038B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10072038-B2 |
| Application number | US-201615545881-A |
| Country | US |
| Kind code | B2 |
| Filing date | Jan 27, 2016 |
| Priority date | Jan 28, 2015 |
| Publication date | Sep 11, 2018 |
| Grant date | Sep 11, 2018 |
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According to the present invention, a crystal of ammonium N-acetylneuraminate anhydrate, and a process for producing a crystal of ammonium N-acetylneuraminate anhydrate, comprising adding or adding dropwise a solvent selected from the group consisting of alcohols and ketones to an aqueous N-acetylneuraminic acid solution containing an ammonium-containing compound and having a pH of 3.0 to 9.0 to precipitate a crystal of ammonium N-acetylneuraminate anhydrate, and collecting the crystal of ammonium N-acetylneuraminate anhydrate from the aqueous solution, can be provided.
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The invention claimed is: 1. A crystal of ammonium N-acetylneuraminate anhydrate. 2. The crystal according to claim 1 , wherein the crystal has peaks at diffraction angles (2θ) of 12.3±0.2°, 13.7±0.2°, 14.2±0.2°, 22.4±0.2°, and 22.6±0.2° in powder X-ray diffraction. 3. The crystal according to claim 2 , wherein the crystal further has peaks at diffraction angles (2θ) of 17.1±0.2°, 21.2±0.2°, 21.6±0.2°, 23.5±0.2°, and 24.8±0.2° in powder X-ray diffraction. 4. The crystal according to claim 3 , wherein the crystal further has peaks at diffraction angles (2θ) of 27.7±0.2°, 28.1±0.2°, 28.4±0.2°, 28.6±0.2°, and 42.3±0.2° in powder X-ray diffraction. 5. A process for producing a crystal of ammonium N-acetylneuraminate anhydrate, comprising adding or adding dropwise a solvent selected from the group consisting of alcohols and ketones to an aqueous N-acetylneuraminic acid solution containing an ammonium-containing compound and having a pH of 3.0 to 9.0 to precipitate a crystal of ammonium N-acetylneuraminate anhydrate, and collecting the crystal of ammonium N-acetylneuraminate anhydrate from the aqueous solution. 6. The production process according to claim 5 , wherein the solvent selected from the group consisting of alcohols and ketones is a solvent selected from C1-C6 alcohols, acetone, methyl ethyl ketone, and diethyl ketone.
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