Complete Workflow for Comprehensive Cannabis Terpenes Analysis
Introduction: Analysis of Terpenes in Cannabis and Hemp
Terpenes are a class of compounds responsible for the aroma or fragrance of the cannabis flower. The search of cannabis customers for a desired aroma or effect makes it important to determine the terpene profile of a cannabis strain. Terpenes have been proposed to enhance the therapeutic properties of cannabinoids through, what is referred to as the entourage effect. The most abundant terpene in cannabis is myrcene. Myrcene is known for its earthy, musky scent and is found in many cannabis varieties. Terpenes quantification can be accomplished using techniques such as gas chromatography (GC) or mass spectrometry.
In the absence of current universal regulatory requirements for terpene testing, this application note is to serve as a guide for customers developing their own analysis for a desired terpene. Herein, we propose a fast and efficient way to determine the terpene profile of hemp or cannabis flowers using a simple sample preparation technique based on liquid extraction. This approach reduces sample preparation time, solvent consumption, and the time to obtain analytical results. This workflow analyzes 31 cannabis-related terpenes by GC/MS in full scan mode and the uses certified reference standards. Tridecane is used as the internal standard as it is not found in the samples and elutes in the middle of the chromatogram. The full scan spectra of the reference standard mix, calibration standards, and samples were searched and matched against the NIST GC/MS spectra library. The method can be easily modified and adapted to include additional terpenes of interest for their identification and quantitation with the same approach.
Chemical Structures of Terpene Analytes
Step | Instructions |
---|---|
1 | Weigh 1.0 g ± 0.001 g of ground hemp flower sample into a 50 mL polypropylene centrifuge tube |
2 | Add 10 mL of GC grade ethyl acetate to each tube and cap |
3 | Sonicate for 15 minutes |
4 | Centrifuge the sample tube at 1252 x g for 5 minutes |
5 | Transfer 1 mL of supernatant to a 2 mL autosampler vial and cap |
Instructions for the Preparation of Internal Standard Solutions
Step | Instructions |
---|---|
1 | Add 3.31 µL of Tridecane into a 25 mL volumetric flask |
2 | Bring up to volume with GC grade ethyl acetate |
3 | Transfer 1 mL of Internal Standard (ISTD) solution into a 2 mL GC autosampler vial |
4 | Place in an appropriate autosampler location to perform sandwich injection addition of Internal Standard |
This makes a 100 ppm [µg/mL] ISTD solution |
Instructions for the Preparation of Working Standard Solutions
Step | Instructions |
---|---|
1 | Transfer 500 µL of Cannabis Terpenes Standard Mix A CRM [2000 µg/mL] to a 10 mL amber vial |
2 | Transfer 500 µL of Cannabis Terpenes Standard Mix B CRM [2000 µg/mL] to the same 10 mL amber vial above |
3 | Add 1.00 mL of GC grade ethyl acetate to the same 10 mL amber vial and cap |
This makes a 500 ppm [µg/mL] working standard solution to prepare dilutions for the instrument calibration curve using the calibration curve standard dilution scheme. Store the working standard solutions and any remaining CRM mixes according to the labeling guidance. |
Calibration Curve Standard Dilution Scheme
Level | Conc. [µg/mL, ppm] | µL of Solution | Solution | µL Ethyl Acetate to add |
---|---|---|---|---|
Cal 1 | 0.75 | 15 | Cal 7 | 985 |
Cal 2 | 1 | 2 | WS | 998 |
Cal 3 | 2 | 4 | WS | 996 |
Cal 4 | 5 | 10 | WS | 990 |
Cal 5 | 10 | 20 | WS | 980 |
Cal 6 | 25 | 50 | WS | 950 |
Cal 7 | 50 | 100 | WS | 900 |
Cal 8 | 70 | 140 | WS | 860 |
Cal 9 | 100 | 200 | WS | 800 |
GC Conditions | |
---|---|
Column | SLB®-5ms 20 m x 0.180 mm ID; 0.18 µM film thickness |
Detector | GC-MS with 9 mm Drawout Lense |
Inlet | 300 °C |
Column Temperature | 45 °C for 2 minutes, then 10 °C/min to 140 °C, Hold at 140 °C for 0.5 minutes then 30°C/min to 300 °C Hold at 300 °C for 2 minutes |
Flow | 0.75 mL/min Constant Flow |
Carrier gas | Helium |
Liner | Single Taper FocusLiner™ with glass wool |
Injection | 2.0 µL – Pulsed Split 50:1 |
Sample Diluent | Ethyl Acetate |
Sample Preparation | Solid-Liquid Extraction with Ethyl Acetate (1 g Cannabis + 10 mL Ethyl Acetate |
Standard Solution | Dilutions of Cannabis Terpenes Mix A and Mix B in Ethyl Acetate (0.75- 100 ppm) with 100 ppm Tridecane as ISTD Sandwich Injection |
Sample | 1-gram hemp flower containing less than 0.3% THC |
Mass Spectrometer Conditions
MS Conditions | |
---|---|
Tuning | Auto-tune |
Acquisition | Full Scan Mode (EI); 40-400 amu |
Solvent Delay | 4 min |
MS Source Temperature | 300 °C |
Quadrupole Temperature | 150 °C |
Electron Energy | 70 eV |
Dwell Time | 50 ms |
TIC Chromatogram of Terpenes Standards Mix
Overlaid EIC of nine α-Pinene standards
Three injections of 50 mg/mL α-Pinene standard
Peak | Compound | Retention Time (min) | Quant (m/z) | Qual 1 (m/z) | Qual 2 (m/z) | Gain |
---|---|---|---|---|---|---|
1 | α-Pinene | 5.260 | 93 | 105 | 121 | 10 |
Level | α-Pinene (μg/mL) |
---|---|
1 | 0.75ppm |
2 | 1ppm |
3 | 2ppm |
4 | 5ppm |
5 | 10ppm |
6 | 25ppm |
7 | 50ppm |
8 | 70ppm |
9 | 100ppm |
Calibration curve for α-Pinene standards from 0.75 µg/ml to 100 µg/ml
Standard Repeatability (0.75 μg/mL/) | Peak Area |
---|---|
STD1 Injection 1 | 3052 |
STD1 Injection 2 | 3262 |
STD1 Injection 3 | 3098 |
Mean | 3137.60 |
Standard Deviation | 110.37 |
RSD (%) | 3.52 |
Linearity, LOD and LOQ | |
---|---|
Concentration (μg/mL) | ISTD Resp. Ratio |
0.75 | 0.016 |
1 | 0.032 |
2 | 0.079 |
5 | 0.183 |
10 | 0.374 |
25 | 0.916 |
50 | 1.814 |
70 | 2.499 |
100 | 3.589 |
LOD | 0.25 μg/mL |
LOQ | 0.75 μg/mL |
GC-MS Detection and Calibration of Camphene
Overlaid EIC of nine Camphene standards
Three injections of 50 mg/mL Camphene standard
Peak | Compound | Retention Time (min) | Quant (m/z) | Qual 1 (m/z) | Qual 2 (m/z) | Gain |
---|---|---|---|---|---|---|
2 | Camphene | 5.551 | 93 | 121 | 79 | 10 |
Level | α-Pinene (g/mL) |
---|---|
1 | 0.75ppm |
2 | 1ppm |
3 | 2ppm |
4 | 5ppm |
5 | 10ppm |
6 | 25ppm |
7 | 50ppm |
8 | 70ppm |
9 | 100ppm |
Calibration curve for α-Terpinene standards from 0.75 µg/ml to 100 µg/ml
Standard Repeatability (0.75 μg/mL/) | Peak Area |
---|---|
STD1 Injection 1 | 1702 |
STD1 Injection 2 | 1660 |
STD1 Injection 3 | 1632 |
Mean | 1665 |
Standard Deviation | 35.41 |
RSD (%) | 2.13 |
Linearity, LOD and LOQ | |
---|---|
Concentration (μg/mL) | ISTD Resp. Ratio |
0.75 | 0.007 |
1 | 0.017 |
2 | 0.043 |
5 | 0.107 |
10 | 0.234 |
25 | 0.616 |
50 | 1.256 |
70 | 1.7726 |
100 | 2.5716 |
LOD | 0.25 μg/mL |
LOQ | 0.75 μg/mL |
GC-MS Detection and Calibration of α-Terpinene
Overlaid EIC of nine α-Terpinene standards
Three injections of 50 mg/mL α-Terpinene standard
Peak | Compound | Retention Time (min) | Quant (m/z) | Qual 1 (m/z) | Qual 2 (m/z) | Gain |
---|---|---|---|---|---|---|
5 | α-Terpinene | 6.726 | 121 | 136 | 105 | 10 |
Level | α-Pinene (g/mL) |
---|---|
1 | 0.75ppm |
2 | 1ppm |
3 | 2ppm |
4 | 5ppm |
5 | 10ppm |
6 | 25ppm |
7 | 50ppm |
8 | 70ppm |
9 | 100ppm |
Calibration curve for α-Terpinene standards from 0.75 µg/ml to 100 µg/ml
Standard Repeatability (0.75 μg/mL/) | Peak Area |
---|---|
STD1 Injection 1 | 1702 |
STD1 Injection 2 | 1660 |
STD1 Injection 3 | 1632 |
Mean | 1665 |
Standard Deviation | 35.41 |
RSD (%) | 2.13 |
Linearity, LOD and LOQ | |
---|---|
Concentration (μg/mL) | ISTD Resp. Ratio |
0.75 | 0.007 |
1 | 0.017 |
2 | 0.043 |
5 | 0.107 |
10 | 0.234 |
25 | 0.616 |
50 | 1.256 |
70 | 1.7726 |
100 | 2.5716 |
LOD | 0.25 μg/mL |
LOQ | 0.75 μg/mL |
Tridecane ISTD Response Reproducibility
Level | Ret. Time [min] | Tridecane ISTD Response |
---|---|---|
1 | 11.050 | 196767 |
2 | 11.050 | 197806 |
3 | 11.051 | 197399 |
4 | 11.051 | 202600 |
5 | 11.051 | 207489 |
6 | 11.049 | 212668 |
7 | 11.049 | 217217 |
8 | 11.050 | 220822 |
9 | 11.050 | 220802 |
% RSD | 0.006 % | 4.82 % |
Overlaid EIC chromatograms of 9 Tridecane ISTD Injections from calibration curve
TIC of Extracted Hemp Sample
Chromatogram of the Extracted Compound from Hemp Sample
Targeted MS Library Created from Cannabis Terpene CRM Mix A & B
MS Spectra of Peak at 13.082 min α-Humulene
Tabulated Results for 31 Cannabis Terpenes and IS | |||||||
---|---|---|---|---|---|---|---|
Peaks | Compound | CAS No. | Ret. Time [min] | Lib Match Factor | r2 | Range [μg/mL] | Detected in hemp sample? |
1 | α-Pinene | 80-56-8 | 5.257 | 98.99 | 0.99991 | 0.75-100 | Y |
2 | Camphene | 79-92-5 | 5.553 | 99.00 | 0.99990 | 0.75-100 | Y |
3 | β-Pinene | 127-91-3 | 6.049 | 99.17 | 0.99995 | 1.50-200 | Y |
4 | 3-Carene | 13466-78-9 | 6.589 | 99.15 | 0.99992 | 1.50-200 | Y |
5 | α-Terpinene | 99-86-5 | 6.726 | 99.62 | 0.99987 | 0.75-100 | Y |
6 | p-Cymene | 99-87-6 | 6.856 | 99.58 | 0.99987 | 0.75-100 | Y |
7 | Limonene | 138-86-3 | 6.938 | 99.21 | 0.99997 | 1.50-200 | Y |
8 | γ-Terpinene | 99-85-4 | 7.422 | 99.35 | 0.99994 | 0.75-100 | Y |
9 | Terpinolene | 586-62-9 | 7.872 | 99.21 | 0.99990 | 0.75-100 | N |
10 | L-Fenchone | 7787-20-4 | 7.930 | 99.47 | 0.99989 | 0.75-100 | Y |
11 | Linalool | 78-70-6 | 8.101 | 99.37 | 0.99915 | 0.75-100 | Y |
12 | Fenchol | 2217-02-9 | 8.426 | 99.43 | 0.99996 | 0.75-100 | Y |
13 | Camphor | 76-22-2 | 8.866 | 99.57 | 0.99997 | 1.50-200 | Y |
14 | Isoborneol | 124-76-5 | 9.126 | 99.45 | 0.99983 | 0.75-100 | Y |
15 | (+)-Borneol | 464-43-7 | 9.259 | 99.36 | 0.99968 | 0.75-100 | Y |
16 | DL-Menthol | 89-78-1 | 9.331 | 99.52 | 0.99988 | 0.75-100 | Y |
17 | α-Terpineol | 10482-56-1 | 9.596 | 99.34 | 0.99942 | 0.75-100 | Y |
18 | Citronellol | 106-22-9 | 10.036 | 99.05 | 0.99961 | 0.75-100 | Y |
19 | Pulegone | 89-82-7 | 10.234 | 99.55 | 0.99956 | 0.75-100 | Y |
20 | Geraniol | 106-24-1 | 10.386 | 98.21 | 0.99946 | 0.75-100 | Y |
21 | Geranyl Acetate | 105-87-3 | 12.145 | 98.64 | 0.99980 | 0.75-100 | Y |
22 | α-Cedrene | 469-61-4 | 12.699 | 99.62 | 0.99997 | 0.75-100 | N |
23 | β-Caryophellene | 87-44-5 | 12.728 | 99.68 | 0.99953 | 0.75-100 | Y |
24 | α-Humulene | 6753-98-6 | 13.082 | 98.90 | 0.99975 | 0.75-100 | Y |
25 | Nerolidol I | 7212-44-4 | 13.636 | 98.73 | 0.99913 | 1.50-200 | Y |
26 | Nerolidol II | 7212-44-4 | 13.845 | 99.19 | 0.99905 | Y | |
27 | Cedrol | 77-53-2 | 14.226 | 99.46 | 0.99978 | 0.75-100 | Y |
28 | β-Eudesmol | 473-15-4 | 14.471 | 99.60 | 0.99945 | 0.75-100 | Y |
29 | α-Bisabolol | 23089-26-1 | 14.594 | 99.62 | 0.99965 | 0.75-100 | Y |
30 | Phytol I | 7541-49-3 | 16.145 | 92.91 | 0.99975 | 0.75-100 | Y |
31 | Phytol II | 7541-49-3 | 16.225 | 92.91 | 0.99950 | Y | |
ISTD | Tridecane | 629-50-5 | 11.050 | 96.17 | ****** | 100 ppm |
Conclusion
A fast, efficient, and highly reproducible analytical method was developed for the quantitative analysis of 31 cannabis-related terpenes using GC-MS. Supelco® chromatography consumables, solvents, supplies, analytical reagents, and certified reference standards in combination with GC-MS provide an efficient way to analyze cannabis products for terpenes to meet the current cannabis product labeling requirements. Low quantitation levels of 0.75 µg/g (750ppb) are easily achieved. Also obtaining all the consumables and reagents from one supplier ensures that time is well spent in analyzing and running samples rather than finding multiple sources for the required analytical supplies. The use of a 20m x 0.18mm x 0.18 μM GC column provides the greatest chromatographic resolution of terpene analytes and facilitates the analysis of additional analytes in the future, if necessary.
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