Method for separating and determining calcipotriol intermediate F and impurities thereof
A technology of calcipotriol and intermediates, applied in the field of analytical chemistry, to achieve the effect of ensuring product quality, strong specificity, and high sensitivity
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Embodiment 1
[0055] (1) Instruments and conditions
[0056] Instrument: high performance liquid chromatography
[0057] Chromatographic column: ODSHYPERSIL (250×4.0mm, 5um)
[0058] Mobile phase: mixed solution of methanol and ethyl acetate
[0059] The volume ratio of methanol to ethyl acetate is 9:1
[0060] Wavelength: 270nm
[0061] Column temperature: 25°C
[0062] Flow rate: 1.5ml / min
[0063] Injection volume: 20μl
[0064] Diluent: Mixed solution of methanol and ethyl acetate
[0065] The volume ratio of methanol to ethyl acetate is 8:2
[0066] (2) Experimental steps
[0067] a) Impurity VD2 reference solution: Take 9.88mg of VD2 reference substance, put it in a 50ml measuring bottle, add 10ml of ethyl acetate to dissolve, add methanol to dilute to the mark, shake well, and you get it.
[0068] b) Impurity E control solution: take 10.14 mg of impurity E reference substance, put it in a 50 ml measuring bottle, add 10 ml of ethyl acetate to dissolve, add methanol to dilute ...
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