Hexahydrocannabinol and closely related semi-synthetic cannabinoids: A comprehensive review.
I. Ujváry
Drug Testing and Analysis June 2, 2023 DOI: 10.1002/dta.3519 (opens in new tab)
Study at a glance
AI-extracted from the abstract| Characteristics | Review Peer reviewed |
|---|---|
| Key findings | The authors review the chemistry, analysis, and pharmacology of hemp-derived semi-synthetic cannabinoids, especially hexahydrocannabinol (HHC) and its acetate (HHC-O). They report that HHC reached the recreational drug market in 2021, is produced from CBD via cyclization and catalytic hydrogenation, and that preclinical studies indicate the (9R)-HHC epimer has THC-like pharmacological properties. They contend that human pharmacology and metabolism of HHC are yet to be investigated and that rapid (immuno)analytical urine detection methods are lacking. |
Abstract
Since the early 2000s, there has been a turmoil on the global illicit cannabinoid market. Parallel to legislative changes in some jurisdictions regarding herbal cannabis, unregulated and cheap synthetic cannabinoids with astonishing structural diversity have emerged. Recently, semi-synthetic cannabinoids manufactured from hemp extracts by simple chemical transformations have also appeared as recreational drugs. The burst of these semi-synthetic cannabinoids into the market was sparked by legislative changes in the United States, where cultivation of industrial hemp restarted. By now, hemp-derived cannabidiol (CBD), initially a blockbuster product on its own, became a "precursor" to semi-synthetic cannabinoids such as hexahydrocannabinol (HHC), which appeared on the drug market in 2021. The synthesis and cannabimimetic activity of HHC were first reported eight decades ago in quest for the psychoactive principles of marijuana and hashish. Current large-scale manufacture of HHC is based on hemp-derived CBD extract, which is converted first by cyclization into a Δ8 /Δ9 -THC mixture, followed by catalytic hydrogenation to afford a mixture of (9R)-HHC and (9S)-HHC epimers. Preclinical studies indicate that (9R)-HHC has THC-like pharmacological properties. The animal metabolism of HHC is partially clarified. The human pharmacology including metabolism of HHC is yet to be investigated, and (immuno)analytical methods for the rapid detection of HHC or its metabolites in urine are lacking. Herein, the legal background for the revitalization of hemp cultivation, and available information on the chemistry, analysis, and pharmacology of HHC and related analogs, including HHC acetate (HHC-O) is reviewed.
Citations in the library
Cited by 9
- Preliminary pharmacokinetic and psychophysical investigations after controlled oral and inhalative consumption of hexahydrocannabinol (HHC) Scientific Reports March 24, 2025
- Cannabimimetic and discriminative stimulus effects of hexahydrocannabinols in mice. Journal of Psychopharmacology July 1, 2025
- HPLC ‐ UV quantitation of synthetically derived THC , THCP , and HHC isomers in commercial vaping liquids and edibles (2019–2024) Journal of Forensic Sciences September 16, 2026
- Synthetic Pathway of Nonpsychoactive Cannabidiol from Psychoactive Tetrahydrocannabinol: A DFT Guide. The Journal of Organic Chemistry July 24, 2026
- In vitro activation of the CB1 receptor by the semi‐synthetic cannabinoids hexahydrocannabinol (HHC), hexahydrocannabinol acetate (HHC‐O) and hexahydrocannabiphorol (HHC‐P) Drug Testing and Analysis June 19, 2024
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