METHOD FOR SIMULTANEOUSLY SEPARATING CANNABIDIVARIN AND CANNABIGEROL

Abstract

The present invention relates to a method for simultaneously separating cannabidivarin and cannabigerol, comprising: sufficiently oscillating a solvent system, allowing the solvent system to stand, and separately collecting an upper phase and a lower phase; dissolving a commercially available industrial hemp full-spectrum refined oil into the upper phase, performing separation using high-speed countercurrent chromatography with the upper phase as a stationary phase and the lower phase as a mobile phase to obtain a mixture of cannabidivarin and the mobile phase and a mixture of cannabigerol and the mobile phase, respectively, and removing the mobile phase to obtain cannabidivarin and cannabigerol. The present invention uses high-speed countercurrent chromatography to simultaneously separate and purify to obtain cannabidivarin (CBDV) with the purity of greater than 98% and cannabigerol (CBG) with the purity of greater than 97% from the industrial hemp full-spectrum refined oil for the first time.

Claims

1. A method for simultaneously separating cannabidivarin and cannabigerol, comprising: sufficiently oscillating a solvent system, allowing the solvent system to stand, and separately collecting an upper phase and a lower phase; dissolving a commercially available industrial hemp full-spectrum refined oil into the upper phase, performing separation using high-speed countercurrent chromatography with the upper phase as a stationary phase and the lower phase as a mobile phase to obtain a mixture of cannabidivarin and the mobile phase and a mixture of cannabigerol and the mobile phase, respectively, and removing the mobile phase to obtain cannabidivarin and cannabigerol, wherein the solvent system is obtained by mixing n-hexane or n-heptane, methyl tert-butyl ether, acetonitrile or ethanol, and water in a volume ratio of 5˜10:1˜3:5˜10:2˜4.

2. The method for simultaneously separating cannabidivarin and cannabigerol according to claim 1, wherein the separately collected upper phase and lower phase are subjected to ultrasonic degassing treatment.

3. The method for simultaneously separating cannabidivarin and cannabigerol according to claim 1, wherein the conditions for the high-speed countercurrent chromatography are: the rotation direction being forward rotation; the rotation speed of 800 rpm; the column temperature of 25° C.; the flow rate of the mobile phase at 5 mL/min; and the detection wavelength of the detector at 214 nm.

4. The method for simultaneously separating cannabidivarin and cannabigerol according to claim 1, wherein the process conditions for removing the mobile phase are: rotary evaporation and vacuum drying at 55° C. and −0.085 MPa.

Description

DESCRIPTION OF EMBODIMENTS

[0018] The present invention is further described below in conjunction with specific Examples. It should be appreciated that these Examples are only used to illustrate the present invention rather than to limit the scope of the present invention. In addition, it should be appreciated that, after viewing the content taught by the present invention, a person skilled in the art can make various changes or modifications to the present invention, and these equivalents also fall within the scope defined by the appended claims of the present application.

[0019] The reagents and apparatus used in the Examples are as follows: [0020] reagents: n-hexane, n-heptane, acetonitrile, ethanol, and methyl tert-butyl ether are all analytical reagents manufactured by Sinopharm Chemical Reagent Co., Ltd.; the water is deionized water; and the industrial hemp full-spectrum refined oil is a commercially available product; and [0021] apparatus: the high-speed countercurrent chromatograph is a model TBE-300C high-speed countercurrent chromatograph manufactured by Shanghai Tauto Biotech Co., Ltd.

Example 1

[0022] N-hexane, methyl tert-butyl ether, acetonitrile, and water were mixed in a volume ratio of 6:3:6:3 to prepare a solvent system. The solvent system was added into a separatory funnel to be sufficiently oscillated, and allowed to stand for phase separation, to obtain a two-phase mixture. The upper and lower phases were collected separately, and placed in an ultrasonic oscillator respectively for ultrasonic degassing. The commercially available industrial hemp full-spectrum refined oil was dissolved into the upper phase. High-speed countercurrent chromatography was employed for separation with the upper phase as a stationary phase and the lower phase as a mobile phase, and the chromatographic conditions were set as follows: forward rotation, the rotation speed of 800 rpm; the column temperature of 25° C.; the flow rate of the mobile phase at 5 mL/min; and the detection wavelength of the detector at 214 nm. The time when sample introduction was finished was counted as 0 min, a mixture of cannabidivarin (CBDV) and the mobile phase was obtained at 140˜200 min, and a mixture of cannabigerol (CBG) and the mobile phase was obtained at 210˜280 min. They were placed in a rotary evaporator under the conditions of water bath temperature of 55° C. and vacuum pressure of −0.085 MPa for rotary evaporation and vacuum drying, and the lower phase was removed, thereby obtaining cannabidivarin (CBDV) and cannabigerol (CBG) products.

[0023] The purity of the products obtained in this example was analyzed by high performance liquid chromatography (HPLC), the results showed that: the purity of cannabidivarin (CBDV) was 98.42%, and the purity of cannabigerol (CBG) was 97.53%.

Example 2

[0024] N-heptane, methyl tert-butyl ether, ethanol, and water were mixed in a volume ratio of 5:3:5:4 to prepare a solvent system. The solvent system was added into a separatory funnel to be sufficiently oscillated, and allowed to stand for phase separation, to obtain a two-phase mixture. The upper and lower phases were collected separately, and placed in an ultrasonic oscillator respectively for ultrasonic degassing. The commercially available industrial hemp full-spectrum refined oil was dissolved into the upper phase. High-speed countercurrent chromatography was employed for separation with the upper phase as a stationary phase and the lower phase as a mobile phase, and the chromatographic conditions were set as follows: forward rotation, the rotation speed of 800 rpm; the column temperature of 25° C.; the flow rate of the mobile phase at 5 mL/min; and the detection wavelength of the detector at 214 nm. The time when finishing sample introduction was finished was counted as 0 min, a mixture of cannabidivarin (CBDV) and the mobile phase was obtained at 100˜140 min, and a mixture of cannabigerol (CBG) and the mobile phase was obtained at 150˜200 min. They were placed in a rotary evaporator under the conditions of water bath temperature of 55° C. and vacuum pressure of −0.085 MPa for rotary evaporation and vacuum drying, and the lower phase was removed, thereby obtaining cannabidivarin (CBDV) and cannabigerol (CBG) products.

[0025] The purity of the products obtained in this example was analyzed by high performance liquid chromatography (HPLC), the results showed that: the purity of cannabidivarin (CBDV) was 98.32%, and the purity of cannabigerol (CBG) was 97.15%.