A method of preparing medicinal magnesium acetate tetrahydrate
A magnesium acetate, medicinal technology, applied in the direction of carboxylate preparation, carboxylate preparation, chemical instruments and methods, etc., can solve problems such as inability to use and products that do not meet the quality standard requirements, and achieve cost saving and convenient storage , The effect of short process flow
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Embodiment 1
[0028] In the reaction flask, add glacial acetic acid 216.2g (2.1 molar equivalent), water 800mL, start mechanical stirring, add magnesium hydroxide 100g (1 molar equivalent), then, heat to 75°C for 1 hour, and cool the reaction solution to room temperature; Adjust the pH value of the solution to 7.70 with magnesium hydroxide, filter, and adjust the pH of the filtrate to 5.22 with glacial acetic acid; the solution is concentrated under reduced pressure, and the density of the concentrated solution is detected. When the density reaches 1.283, the concentration is stopped, and the concentrated solution is stirred at room temperature Crystallization; after about 6 hours of crystallization, filter, and wash the filter cake with 100 mL of absolute ethanol; finally, place it in a blast drying oven at 50°C for 3 hours to obtain the finished product.
Embodiment 2
[0030] In the reaction flask, add glacial acetic acid 216.2g (2.1 molar equivalent), water 800mL, start mechanical stirring, add magnesium hydroxide 100g (1 molar equivalent), then heat to 80°C for 0.5h, and cool the reaction solution to 35°C Below; use magnesium hydroxide to adjust the pH value of the solution to 8.31, filter, and use glacial acetic acid to adjust the pH of the filtrate to 5.21; this solution is concentrated under reduced pressure, and the density of the concentrated solution is detected. When the density reaches 1.284, stop concentrating and leave the concentrated solution at room temperature Stir and crystallize at low temperature; after 5 hours of crystallization, filter, and wash the filter cake with 100 mL of absolute ethanol; finally, place it in a blast drying oven at 50°C for 4 hours to obtain the finished product.
Embodiment 3
[0032] In the reaction flask, add glacial acetic acid 216.2g (2.1 molar equivalent), water 800mL, start mechanical stirring, add magnesium hydroxide 100g (1 molar equivalent), then heat to 78°C, react for 1.5h, and cool the reaction liquid to 25 ℃; use magnesium hydroxide to adjust the pH value of the solution to 9.0, filter, and use glacial acetic acid to adjust the pH value of the filtrate to 5.22; this solution is concentrated under reduced pressure, and the temperature during the reduced pressure concentration is 80°C, and the density of the concentrated solution is detected. When the concentration reaches 1.281, the concentration is stopped, and the concentrated solution is stirred and crystallized at room temperature; after 7 hours of crystallization, filter, and the filter cake is washed with 100 mL of absolute ethanol; finally, it is placed in a blast drying oven at 55°C for 2 hours to obtain the finished product .
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