Method for quickly extracting aspidinol
A fast technology, which is applied in the field of rapid separation and extraction of cotton horse phenol, can solve the problems of not finding and separating cotton horse phenol, limiting the wide application of C.
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Embodiment 1
[0014] Add 2.5kg of Trichophyllum powder after passing through an 80 mesh sieve, add 20L of 50% ethanol, cold soak overnight, filter and recover under reduced pressure to obtain a paste sample, add n-hexane for repeated extraction, recover the extract under reduced pressure, and set the volume to 1L. Add 1% NaOH solution to dissolve the phenolic substances. After fully dissolving, add 1% HCL solution after separating the water layer through the separating funnel to reduce the phenolic substances, then use ethyl acetate to extract the aqueous layer to separate the phenolic substances, combine the extraction layers, and reduce After pressure recovery, wash pure solution to wash pure. The purity of GC-MS is 65.824%.
Embodiment 2
[0016] Add 2.5kg of Trichophyllum powder passed through an 80-mesh sieve to 20L of 70% ethanol, cold-soak overnight, filter and recover under reduced pressure to obtain a paste sample, add n-hexane for repeated extraction, recover the extract under reduced pressure, and set the volume to 1L. Add 2% NaOH solution to dissolve the phenolic substances. After fully dissolving, add 2% HCL solution to reduce the phenolic substances after the water layer is separated by a separatory funnel, then use ethyl acetate to extract the aqueous layer to separate the phenolic substances, and repeat the above-mentioned alkali extraction. In the sinking step, the extraction layers were combined, and after recovery under reduced pressure, they were washed with the pure solution, and the GC-MS detection purity reached 83.373%.
Embodiment 3
[0018] Add 2.5kg of Trichophyllum powder after passing through an 80-mesh sieve, add 20L of 80% ethanol, cold-soak overnight, filter and recover under reduced pressure to obtain a paste sample, add n-hexane for repeated extraction, extract under reduced pressure and recover, and set the volume to 1L. Add 3% NaOH solution to dissolve the phenolic substances. After fully dissolving, add 3% HCL solution to reduce the phenolic substances after separating the water layer through the separatory funnel, then use ethyl acetate to extract the aqueous layer to separate the phenolic substances, and repeat the above-mentioned alkali extraction. Sink twice, combine the extraction layers, recover under reduced pressure, wash with the pure solution, and the GC-MS detection purity reaches 92.051%, the results are shown in figure 2 .
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