- Open Access
Cannabinoid crystal polymorphism
Journal of Cannabis Research volume 4, Article number: 23 (2022)
Because cannabinoids are usually amorphous solids, the thought that some of them may also exist in distinctly different crystal polymorphic forms might at first seem unusual. However, this commentary provides compelling evidence and precedent for the likely existence of cannabinoid crystal polymorphism.
The structurally diverse substances comprising the ever-growing collection of cannabinoids (alternatively “phytocannabinoids”) found in Cannabis have been characterized by numerous spectroscopic tools over many decades (Radwan et al. 2021). One conspicuous omission in these methods has often been the examination of cannabinoid crystallinity and the reason for this is simple. After more than a century of cannabinoid investigation, most of them have been routinely described as low melting (usually less than 75 °C) seemingly “amorphous” solids. Consequently, the proposal that any cannabinoid might exist in multiple crystal forms known as “polymorphs” would seem very unlikely. However, the purpose of this commentary is to challenge that perception and explore the possibility of cannabinoid crystal polymorphism.
As mentioned, crystal polymorphism is defined as the existence of one or more distinctly different crystal forms of the same substance and it can manifest itself with both complex and uncomplicated molecules. Whatever the structural details, crystal polymorph creation is controlled by the intricate choreography of both nucleation kinetics and thermodynamic stability. Historically, it is commonly accepted that crystal polymorphism was first discovered for the very simple compound benzamide by the collaboration of noteworthy nineteenth century chemists Friedrich Wohler and Justus von Liebig in 1832. One can only imagine their amazement as they surprisingly observed the fine needles of one benzamide crystal polymorph convert to the rhombic crystals of another polymorph. Almost two centuries later, benzamide crystal polymorphism continues to fascinate current researchers (Kras et al. 2021). A myriad of crystal forms have now been characterized for many substances and thousands of them have been archived as X-ray crystal determinations in the voluminous Cambridge Structural Database (van de Streek 2006).
Cannabinoid crystal polymorphism
Before addressing cannabinoid crystal polymorphism, it is useful to first consider which cannabinoids in Cannabis have even been analyzed as single crystalline entities? To answer this question, a literature search was performed using the Cambridge Structural Database as well as the SciFinder® chemistry database. Of the many cannabinoids in Cannabis, only a few have been characterized by X-ray crystal analysis and they include: delta-9-tetrahydrocannabinolic acid A (THCA-A) (Skell et al. 2021), delta-9-tetrahydrocannabinolic acid B (THCA-B) (Rosenqvist and Ottersen 1975), cannabidiol (CBD) (Mayr et al. 2017; Jones et al. 1977; Ottersen et al. 1977a), cannabinol (CBN) (Ottersen et al. 1977b), and cannabigerol (CBG) (Fettinger et al. 2020). Regarding polymorphism in general, it can be seen in Fig. 1 that growth of the crystal polymorphism literature (both journal articles and patents in SciFinder®) has dramatically increased, nearly quadrupling in the past 20 years. An exhaustive literature review was also performed to learn if any cannabinoid crystal polymorphs have been described? This search was conducted not only on the large number of publications captured under “cannabinoids” in general but also the very specific cannabinoids: THCA-A, delta-9-tetrahydrocannabinol (THC), cannabidiolic acid (CBDA), CBD, cannabigerolic acid (CBGA), CBG, cannabinolic acid (CBNA), CBN, cannabichromenic acid (CBCA), and cannabichromene (CBC). Unfortunately, this effort was greatly complicated by the many papers related to cannabinoid gene polymorphism. Excluding the special case of cocrystal polymorphs (Aitipamula et al. 2014) and any errors of omission due to the complexity of the literature search, it would appear that no fully characterized Cannabis cannabinoid crystal polymorph has yet been reported. However, there have been several intriguing clues in the literature that cannabinoid crystal polymorphism may well be possible (Fig. 2).
Interestingly, the cannabinoid receptors have been an important docking location for several structurally diverse compounds which have exhibited crystal polymorphism. The lipid N-palmitoylethanolamine  is an agonist at the type 2 cannabinoid receptor (CB-2). Two crystal polymorphs (designated α and β) of it were discovered and characterized by X-ray crystallography (Kamlekar and Swamy 2006). Also, the synthetic heterocycle rimonabant  is an inverse agonist at the type 1 cannabinoid receptor (CB-1) and has also demonstrated crystal polymorphism (Fours et al. 2015). However, even more compelling and direct evidence suggests that the basic cannabinoid structural framework itself has the capacity for crystal polymorphism as well. It was discovered 40 years ago that the synthetic 9-ketocannabinoid derivative nabilone  displayed crystal polymorphism. One of the earliest studies utilizing solid state carbon-13 NMR spectroscopy characterized several crystal polymorphic forms of nabilone (Byrn et al. 1985). Furthermore, the THC naphthoyl ester derivative  was just reported to exist in as many as eight different crystal polymorphic forms, designated A-H (Hallow et al. 2021). These separate crystal structures were analyzed by combinations of differential scanning calorimetry (DSC), thermal gravimetric analysis (TGA) as well as powder X-ray diffraction (PXRD). One crystal polymorph of 4 reportedly had a penchant for easily forming solvates and several of its crystal polymorphs were found to be interconvertible.
Importantly, the discovery of cannabinoid crystal polymorphs would clearly be of more than mere academic interest. The very real possibility exists that such cannabinoid crystal polymorphs might possess greater stability or possibly improved bioavailability properties. It has been stated (Haleblian and McCrone 1969) that “probably every organic medicinal can exist in different polymorphs.” Also, in his recent X-ray crystal determination of THCA-A, internationally recognized Brandeis crystallographer Bruce Foxman speculated that this X-ray study with its important information about intermolecular cannabinoid hydrogen bonding would facilitate “the search for polymorphs” (Skell et al. 2021).
Based on the foregoing evidence, it is reasonable to conclude that at least some Cannabis cannabinoids will also exhibit crystal polymorphism.
Availability of data and materials
Cannabinoid receptor type 1
Cannabinoid receptor type 2
Differential scanning calorimetry
Nuclear magnetic resonance
Powder X-ray diffraction
Thermal gravimetric analysis
Delta-9-tetrahydrocannabinolic acid A
Delta-9-tetrahydrocannabinolic acid B
Aitipamula S, Chow PS, Tan RBH. Polymorphism in cocrystals: a review and assessment of its significance. CrystEngComm. 2014;16:3451–65.
Byrn SR, Gray G, Pfeiffer RR, Frye J. Analysis of solid-state carbon-13 NMR spectra of polymorphs (benoxaprofen and nabilone) and pseudopolymorphs (cefazolin). J Pharm Sci. 1985;74:565–8.
Fettinger JC, Condron CL, Coffin MT. Cambridge Structural Database Communication. 2020; Database UHIHEB:Deposition Number 1985628.
Fours B, Cartigny Y, Petit S, Coquerel G. Formation of new polymorphs without any nucleation step. Desolvation of the rimonabant monohydrate: directional crystallization concomitant to smooth dehydration. Faraday Discuss. 2015;179:475–88.
Haleblian J, McCrone W. Pharmaceutical applications of polymorphism. J Pharm Sci. 1969;58:911–29.
Hallow DM, Iuliucci M, Mkrtchyan G, Carino SA, et al. Polymorphs of delta-9-THC naphthoyl ester. WO 2021/076633 A1. 2021.
Jones PG, Falvello L, Kennard O, Sheldrick GM, et al. Cannabidiol. Acta Crystallographica B. 1977;B33:3211–4.
Kamlekar RK, Swamy MJ. Molecular packing and intermolecular interactions in two structural polymorphs of N-palmitoylethanolamine, a type 2 cannabinoid receptor agonist. J Lipid Res. 2006;47:1424–33.
Kras W, Carletta A, Montis R, Sullivan RA, et al. Switching polymorph stabilities with impurities provides a thermodynamic route to benzamide form III. Commun Chem. 2021;4:Article 38.
Mayr T, Grassl T, Korber N, Christoffel V, et al. Cannabidiol revisited. IUCrData. 2017;2:170276.
Ottersen T, Rosenqvist E, Turner CE, El-Feraly FS. The crystal and molecular structure of cannabidiol. Acta Chem Scand B. 1977a;B31:807–12.
Ottersen T, Rosenqvist E, Turner CE, El-Feraly FS. The crystal and molecular structure of cannabinol. Acta Chem Scand B. 1977b;B31:781–7.
Radwan MM, Chandra S, Gul S, ElSohly MA. Cannabinoids, phenolics, terpenes and alkaloids of Cannabis. Molecules. 2021;26:Article 2774.
Rosenqvist E, Ottersen T. The crystal and molecular structure of delta-9-tetrahydrocannabinolic acid B. Acta Chem Scand B. 1975;B29:379–84.
Skell JM, Kahn M, Foxman BM. Delta-9-tetrahydrocannabinolic acid A, the precursor to delta-9-tetrahydrocannabinol (THC). Acta Crystallographica C. 2021;C77:84–9.
van de Streek J. Searching the Cambridge Structural Database for the “best” representative of each unique polymorph. Acta Crystallographica B. 2006;B62:567–79.
Ethics approval and consent to participate
Consent for publication
The author declares that he has no competing interest.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
About this article
Cite this article
Filer, C.N. Cannabinoid crystal polymorphism. J Cannabis Res 4, 23 (2022). https://doi.org/10.1186/s42238-022-00131-2