Method for detecting chemical components of ether extract of bitter gourd leaves
A detection method, a technology of chemical composition, applied in the field of comprehensive development of plant resources
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Embodiment 1
[0037] Bitter Melon Leaf Ether Extract:
[0038] Weigh 2 g of fresh bitter melon leaves that have passed through, grind them into powder, add 200 mL of ether, and repeatedly extract with a Soxhlet extractor until it is colorless, remove the solvent with a rotary evaporator, weigh the obtained extract, and redissolve the extract in 100mL of diethyl ether; then take 10mL of diethyl ether extract, add 1ml of diethyl ether-n-hexane mixture with a volume ratio of 2:1, 5ml of methanol, 1ml of 0.8mol / L potassium hydroxide methanol solution, shake well, let stand for 5min, add 5ml of water, 300rPm Centrifuge for methyl esterification, take the supernatant for GC-MS analysis.
Embodiment 2
[0040] Adopt GC-MS to analyze, gas chromatography conditions:
[0041] The initial temperature of the column is 60°C for 2 minutes, raised to 150°C at 5°C / min and held for 3 minutes, then raised to 220°C at 10°C / min and held for 3 minutes, the temperature of the injection port: 250°C; High-purity helium was used as the carrier gas, the flow rate was 1.0ml / min, the split ratio was 60:1, and the injection volume was 1.0 μL.
[0042] Mass spectrometry conditions: mass spectrometry ionization mode is EI, electron energy of electron bombardment source is 70eV, ion source temperature is 250°C; electron multiplier voltage is 1.0×10 5 ; Solvent delay time: 3min; Scanning range m / z: 35-1000aum.
[0043] According to the above-mentioned GC-MS analysis conditions, the bitter melon leaf alcohol-soluble components are tested on the machine, and the total ion current chromatogram of the bitter melon leaf ether extract (see figure 1). The identification of each peak was mainly through the...
Embodiment 3
[0045] (1) Bitter melon leaf ether extract:
[0046] Weigh 2g of fresh balsam pear leaves and grind them into powder, add 200mL of diethyl ether, repeatedly extract with a Soxhlet extractor until colorless, remove the solvent, weigh, and re-dissolve the extract in 100mL of diethyl ether; then take 10mL of ether extract, Add 1ml of diethyl ether-n-hexane mixture with a volume ratio of 2:1, 5ml of methanol, and 1ml of 0.8mol / L potassium hydroxide methanol solution, shake well, let stand for 5min, add 5ml of water, centrifuge at 300rpm, carry out methyl esterification treatment, and set aside;
[0047] (2) Analyze by GC-MS, gas chromatographic conditions: the initial column temperature is 60°C for 2 minutes, rise to 150°C at 5°C / min and hold for 3 minutes, then rise to 220°C at 10°C / min, hold for 3 minutes, inject the sample Inlet temperature: 250°C, mass spectrometry connection line temperature: 250°C, high-purity helium as carrier gas, flow rate 1.0ml / min, split ratio: 60:1, in...
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