A fingerprint detection method of ginger essential oil
A fingerprint spectrum and detection method technology, applied in the field of detection and analysis, can solve problems such as long detection time and poor qualitative effect, and achieve the effects of reducing detection cost, facilitating identification, and avoiding thermal retake and thermal conversion effects.
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Embodiment 1
[0035] Establish standard reference fingerprint of ginger essential oil
[0036] Take 100 μL of ginger essential oil, add n-hexane to 1 mL to obtain the pure ginger essential oil dilution, pass through a 0.22 μm organic filter membrane and enter it into a convergent chromatograph for detection by a PDA detector (wavelength collection range: 200-310 nm).
[0037] Convergence chromatographic conditions: Acqtity UPC 2 BEH column (50 mm×2.1 mm, 1.8 μm), PDA detector, system back pressure is 2000 psi, column temperature is 40 ℃, column flow rate is 0.8 mL / min, mobile phase is supercritical CO 2 (Mobile phase A) and acetonitrile-methanol solution (mobile phase B) with a volume ratio of 1:1, initial mobile phase is 100% A, gradient elution, collection wavelength range 200 nm ~ 310 nm, injection volume is preferably 4.0 μL.
[0038] Gradient elution conditions: initial mobile phase hold for 2 min; 2 ~ 3 min, 100% A ~ 99.8% A, hold for 2 minutes; 5 ~ 6 min, 99.8% A ~ 99.5% A, hold for 2 min; ...
Embodiment 2
[0042] Sample: ginger essential oil
[0043] 1. Take 100 μL of ginger essential oil to be tested, add n-hexane to 1 mL to obtain a dilution of ginger essential oil to be tested, and pass through a 0.22μm organic filter membrane for injection;
[0044] 2. The ginger essential oil dilution to be tested is tested by a convergence chromatograph, combined with the PDA detector to determine the convergence chromatographic fingerprint of the ginger essential oil to be tested, see figure 2 .
[0045] Convergence chromatographic conditions: Acqtity UPC 2 BEH column (50 mm×2.1 mm, 1.8 μm), PDA detector, system back pressure is 2000 psi, column temperature is 40 ℃, column flow rate is 0.8 mL / min, mobile phase is supercritical CO 2 (Mobile phase A) and acetonitrile-methanol solution (mobile phase B) with a volume ratio of 1:1, initial mobile phase is 100% A, gradient elution, collection wavelength range 200 nm ~ 310 nm, injection volume is preferably 4.0 μL.
[0046] Gradient elution conditions:...
Embodiment 3
[0049] Sample: soybean oil
[0050] 1. Take 100 μL of soybean oil, add n-hexane to 1 mL to obtain the soybean oil dilution to be tested, and pass the 0.22 μm organic filter membrane to be injected;
[0051] 2. The soybean oil diluent to be tested is tested by a convergence chromatograph, combined with a PDA detector to obtain the convergence chromatographic fingerprint of soybean oil, see image 3 .
[0052] Convergence chromatographic conditions: Acqtity UPC 2 BEH column (50 mm×2.1 mm, 1.8 μm), PDA detector, system back pressure is 2000 psi, column temperature is 40 ℃, column flow rate is 0.8 mL / min, mobile phase is supercritical CO 2 (Mobile phase A) and acetonitrile-methanol solution (mobile phase B) with a volume ratio of 1:1, initial mobile phase is 100% A, gradient elution, collection wavelength range 200 nm ~ 310 nm, injection volume is preferably 4.0 μL.
[0053] Gradient elution conditions: initial mobile phase hold for 2 min; 2 ~ 3 min, 100% A ~ 99.8% A, hold for 2 minutes;...
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