A kind of detection method of benzohydroxamic acid in flour and flour improver
A technology of flour improver and benzohydroxamic acid, which is applied in the field of analytical chemistry, can solve the problems of unused flour and flour improver research, and achieve good dissolution effect, high recovery rate and precision, and good separation effect
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Embodiment 1
[0025] 1 μg / mL of benzoxamic acid standard solution, accurate injection of 50 μL, Shimadzu InertSustain C18 (250 mm×4.6 mm, 5 μm) column separation, methanol (A) and pH 2.5 of 18 mM potassium dihydrogen phosphate solution (B) gradient elution, elution procedure see Table 1; flow rate 1 mL / min, column temperature 30 °C, UV detector wavelength of 228 nm, according to the above liquid chromatography conditions, benzohydroxamic acid retention time of 16.12 min.
[0026] Boom 1 gradient elution procedure
[0027]
Embodiment 2
[0029]Weigh 2.0g (accurate to 0.01g) homogeneous flour, add 8mL methanol / water (6:4, volume ratio) solution, vortex mixing, ultrasonic extraction for 20min, 4000r / min centrifugation for 3min; after taking the supernatant film, to be measured; different pH flow relative to the impurities in wheat flour have a greater impact, At pH 2.0, the separation degree between the target and the sample impurities < 1.5; at pH 2.5, the separation degree between the target and the sample impurities was 4.85; at pH 3.0, the separation between the target and the sample impurities was 4.70; at pH 4.0, the separation between the target and the sample impurities was 3.35; at pH5.0, the separation between the target and the sample impurities was 1.91; therefore, the 18mM potassium dihydrogen phosphate at pH2.5 was the mobile phase, which made benzoxamic acid and wheat flour impurities best separated, of which the benzohydroxamic acid retention time was 16.12min, and the impurity peak retention time in...
Embodiment 3
[0031] Weigh 2.0g (accurate to 0.01g) homogeneous flour sample in a 50mL plastic centrifuge tube, add 100 μg / mL benzohydroxamic acid standard intermediate solution 0.1mL, let stand for a period of time, add 8mL of different proportions of methanol / aqueous solution (volume ratios are 10:0, 9:1, 8:2, 7:3, 6:4, 5:5, 4:6, 3:7, 2:8, 1:9, 0:10), vortex mixing, ultrasonic extraction 20min, 4000r / According to the above liquid chromatography conditions, the retention time of the target peak in the sample is consistent with the standard, and the recovery rate of methanol / water is the highest at 6:4, which is 84.8%.
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