Celastrus angulatus active compound, emulsion in water and preparation method thereof
A technology of picroderm and water emulsion, applied in the field of plant pesticides, can solve the problems of low content of active ingredients, single preparation, large pollution, etc., and achieve the effect of simple operation, simple process and reduced usage
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Embodiment 1
[0048] (1) Preparation of the original drug of phareidin
[0049] Weigh 20g of bitter bark root bark from Gansu, crush it through a 30-mesh sieve, put it into a 500mL reaction bottle, add 125g of toluene, 135g of xylene, heat to 90°C and stir for 5 hours, cool and filter, collect the filtrate, repeat the operation three times to combine The filtrate was evaporated and desolvated to obtain 2.01g of extract, added 4g of silica gel (fineness: about 300 mesh, the same below) to absorb, put it into a chromatographic column (1.5×30cm, filled with 30g of silica gel), rinsed with 300mL of absolute ethanol, The eluents were combined, and 1.76 g of solids were obtained by desolventization. Add 3 g of silica gel for adsorption and put them into a chromatographic column (1.5 × 30 cm, filled with 30 g of silica gel) for chromatographic separation. Use petroleum ether-ethyl acetate system, 10:1 (volume ratio, the same below) to collect 1 to 3 copies (20 mL each, the same below); 8:1 to coll...
Embodiment 2
[0078] The preparation method and stability analysis of the original medicine of picroderm and emulsion in water
[0079] (1) Paretinin original drug
[0080] Weigh 100g of vine roots and bark purchased from Hubei, crush them through a 30-mesh sieve, put them into a 2000mL reaction bottle, add 250g of toluene, 350g of xylene, heat to 90°C and reflux for 4 hours, cool and filter, collect the filtrate, repeat the operation three times to combine The filtrate was evaporated and desolvated to obtain 12.6g of extract, added 20g of silica gel (fineness is about 300 mesh, the same below) to absorb, put it into a chromatographic column (3×60cm, filled with 100g of silica gel), rinsed with 500mL of absolute ethanol, The eluents were combined, and 11.2 g of solids were obtained by desolventization. After being absorbed by 15 g of silica gel, they were loaded into a chromatographic column (3×60 cm, filled with 100 g of silica gel) for chromatographic separation, using petroleum ether-eth...
Embodiment 3
[0109] Screening of Surfactants for Erythrocetin in Water Emulsion
[0110] Take 3.72g of the homemade phaelopedin original drug, add 21.2g of surfactant, heat to 51°C, stir (1500r / min) for 10 minutes to obtain an organic phase, mix 4.8g of ethylene glycol, 0.25g of xanthan gum, 0.1g silicone antifoam agent, make up tap water to 120g and combine to obtain the water phase, at a temperature of 55°C, under stirring (2500r / min), slowly and evenly add the water phase (3 drops per second) to the organic phase, drop Continue to stir for 20 minutes after the addition to obtain an emulsion, and ultrasonicate the emulsion on a high-speed ultrasonic homogenizer (frequency 20KHz) for 8 minutes to obtain a phaevalin aqueous emulsion.
[0111] The surfactants used are as shown in the figure below, and the emulsion stability test is carried out according to GB-T1603-2001; the low-temperature stability test is carried out according to GB-T19137-2003; the high-temperature storage stability tes...
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