Rapid detection method of triethanolamine ester
A detection method, the technology of ethanolamine ester, applied in the field of analysis and detection, can solve the problems of cumbersome process and expensive nuclear magnetic resonance equipment, etc., and achieve the effect of convenient and simple operation, low measurement cost and short measurement time
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Embodiment 1
[0038] The rapid detection method of a kind of triethanolamine ester of the present embodiment adopts high-performance liquid chromatography detection, comprises the steps:
[0039] (1) Preparation of the test solution
[0040] Accurately weigh 0.2 g (accurate to 0.0001 g) of the triethanolamine ester sample into a 25 mL volumetric flask, use mobile phase to constant volume, and obtain the test solution after filtering through a 0.45 μm organic microporous membrane;
[0041] (2) Determination
[0042] Draw 50 μ L of the test solution and inject it into a high-performance liquid chromatograph for determination, and quantify by the area normalization method;
[0043] The chromatographic conditions are: mobile phase: n-hexane: isopropanol = 50:50 (volume ratio);
[0044] Column: XB-NH 2 5μm 4.6*250mm;
[0045] Detection wavelength: 210nm;
[0046] The detector is an ultraviolet detector;
[0047] The flow rate is 0.4mL / min;
[0048] Column temperature: room temperature. ...
Embodiment 2
[0050] Example 2 Condition screening and methodological verification
[0051] 1. Experimental drugs and instruments
[0052] 1.1 n-Hexane Chromatographically pure
[0053] 1.2 Isopropanol Chromatographically pure
[0054] 1.3 Triethanolamine ester samples commercially available and self-made
[0055] 1.4 Ultrasonic cleaner
[0056] 1.5 Electronic balances, pipettes, measuring cylinders, and volumetric bottles with a precision of 0.0001 grams
[0057] 1.60.45μm organic solvent filter
[0058] 1.7 Shimadzu LC-10AT high performance liquid chromatograph, SPD-20A detector (quantitative loop 20μL)
[0059] 1.8XB-NH 2 5μm 4.6*250mm chromatographic column
[0060] 2. Chromatographic conditions and preparation
[0061] 2.1 Mobile phase preparation:
[0062] Make n-hexane and isopropanol into the mobile phase at a ratio of 50:50 (volume ratio), filter with a 0.45 μm organic filter membrane, and then sonicate for 15-20 minutes.
[0063] 2.2 Sample handling:
[0064] Accuratel...
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