N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester useful as a sweetener with a high potency of sweetness, is provided in the crystalline form having a high stability and a good purity which is favorable as a commercial product.
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1. A crystal of N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester, wherein said crystal is selected from the group consisting of:(a) a crystal of N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester, which exhibits
1. A crystal of N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester, wherein said crystal is selected from the group consisting of:(a) a crystal of N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester, which exhibits at least X-ray diffraction peaks at diffraction angles of 8.2°, 14.7°, 20.5° and 22.4° (2 θ, CuK α ray) when examined by powder X-ray diffractometry;(b) a crystal of N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester, which exhibits at least X-ray diffraction peaks at diffraction angles of 4.8°, 7.3°, 9.9° and 20.0° (2 θ, CuK α ray) when examined by powder X-ray diffractometry; and(c) a crystal of N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester, which exhibits at least X-ray diffraction peaks at diffraction angles of 4.7°, 8.0°, 9.0°, 14.0°, 20.2° and 24.3° (2 θ, CuK α ray) when examined by powder X-ray diffractometry. 2. A crystal of N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester, which exhibits at least X-ray diffraction peaks at diffraction angles of 8.2°, 14.7°, 20.5° and 22.4° (2 θ, CuK α ray) when examined by powder X-ray diffractometry. 3. A crystal of N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester, which exhibits at least X-ray diffraction peaks at diffraction angles of 4.8°, 7.3°, 9.9° and 20.0° (2 θ, CuK α ray) when examined by powder X-ray diffractometry. 4. A crystal of N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester, which exhibits at least X-ray diffraction peaks at diffraction angles of 4.7°, 8.0°, 9.0°, 14.0°, 20.2° and 24.3° (2 θ, CuK α ray) when examined by powder X-ray diffractometry. 5. A method of making the crystal of claim 2, comprising crystallizing N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester from a solvent comprising an organic solvent and water, wherein said organic solvent is selected from the group consisting of methanol, ethanol, isopropanol, acetone, tetrahydrofuran, and acetonitrile. 6. A method of making the crystal of claim 3, comprising crystallizing N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester from a solvent which is substantially free of water, wherein said solvent is a mixed solvent comprising a first solvent and a second solvent and wherein said first solvent is selected form the group consisting of methanol, ethanol, isopropanol, acetone, tetrahydrofuran, and acetonitrile and said second solvent is selected form the group consisting of methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate, butyl acetate, diethyl ether, methyl t-butyl ether, and toluene. 7. A method of making the crystal of claim 4, comprising crystallizing N-[N-[3-(3-hydroxy-4-methoxyphenyl)propyl]-L-α-aspartyl]-L-phenylalanine 1-methyl ester from a solvent comprising an organic solvent and water, wherein said solvent is a mixed solvent comprising a first solvent and a second solvent and wherein said first solvent is selected from the group consisting of methanol, ethanol, isopropanol, acetone, tetrahydrofuran, and acetonitrile and said second solvent is selected from the group consisting of methyl acetate, ethyl acetate, propyl acetate, isopropyl acetate, butyl acetate, diethyl ether, methyl t-butyl ether, and toluene. 8. A method of sweetening a food or beverage product, comprising incorporating the crystal of claim 1 into a food or a beverage product. 9. A method of sweetening a food or beverage product, comprising incorporating the crystal of claim 2 into a food or a beverage product. 10. A method of sweetening a food or beverage product, comprising incorporating the crystal of claim 3 into a food or a beverage product. 11. A method of sweetening a food or beverage product, comprising incorporating the crystal of claim 4 into a food or a beverage product.
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Straub, Alexander; Lampe, Thomas; Pohlmann, Jens; Rohrig, Susanne; Perzborn, Elisabeth; Schlemmer, Karl Heinz; Pernerstorfer, Joseph, Substituted oxazolidinones and their use in the field of blood coagulation.
Straub, Alexander; Lampe, Thomas; Pohlmann, Jens; Röhrig, Susanne; Perzborn, Elisabeth; Schlemmer, Karl-Heinz; Pernerstofer, Josef, Substituted oxazolidinones and their use in the field of blood coagulation.
Straub, Alexander; Lampe, Thomas; Pohlmann, Jens; Röhrig, Susanne; Perzborn, Elisabeth; Schlemmer, Karl-Heinz; Pernerstorfer, Joseph, Substituted oxazolidinones and their use in the field of blood coagulation.
Straub, Alexander; Lampe, Thomas; Pohlmann, Jens; Röhrig, Susanne; Perzborn, Elisabeth; Schlemmer, Karl-Heinz; Pernerstorfer, Joseph, Substituted oxazolidinones and their use in the field of blood coagulation.
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