Use of starch in preparation of chromatographic separating medium
A technology of chromatographic separation and starch, which is applied in other chemical processes, chemical instruments and methods, etc., can solve the problems that starch is used as a chromatographic separation medium and has not been reported.
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Embodiment 1
[0020] Embodiment 1: to the separation of pigment
[0021] Bromocresol Green 0.0015g, Sudan III 0.0045g, 100 mesh wheat starch 15g were packed in the column.
[0022] Dissolve bromocresol green and Sudan III pigments in a test tube with a small amount of methanol, and load the sample on the starch column by wet method, and the eluent is methanol. The two pigment solutions were collected separately in Erlenmeyer flasks, and the separation effect was as follows: Figure 1 to Figure 4 As shown, it can be seen that using wheat starch, bromocresol green and Sudan III can be effectively separated.
Embodiment 2
[0023] Embodiment 2: to the separation of rutin, quercetin
[0024] Put 15g of sweet potato starch in the column, beat evenly, mix 5mg of rutin with 5mg of quercetin, dissolve in methanol, and load the sample by wet method. First use ethyl acetate as the eluent, cooperate with TLC inspection, and when there are no spots of quercetin, change methanol as the eluent, collect the eluent, cooperate with TLC inspection, and stop the elution when there are no spots of rutin.
[0025] Developing agent: n-butanol-acetic acid-water=4:1:5 (above)
[0026] Chromogen: iodine vapor fumigation
[0027] like Figure 5 As shown, 1 is the rutin reference substance; 2 is the quercetin reference substance; 3 is the rutin MeOH eluent; 4 is the quercetin EtOAc eluent.
Embodiment 3
[0028] Embodiment 3: Separation of harpagoside and harpagoside
[0029] Put 15g of potato starch in the column, beat evenly, mix 5mg of harpagoside with 5mg of harpagoside, dissolve in methanol, and load the sample by wet method. First use ethyl acetate as the eluent, cooperate with TLC inspection, and when there are no harpagoside spots, change methanol as the eluent, collect the eluate, cooperate with TLC inspection, and stop the elution when there are no harpagoside spots.
[0030] Developing solvent: ethyl acetate-ethanol-water=4:1:0.5
[0031] Chromogen: 2% vanillin sulfuric acid solution
[0032] like Figure 5 As shown, 1 is the reference substance of harpagoside; 2 is the reference substance of harpagoside; 3 is the eluent of harpagoside MeOH; 4 is the eluent of harpagoside EtOAc.
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