Jump to content

Hexahydrocannabihexol

From Wikipedia, the free encyclopedia

Hexahydrocannabihexol
Identifiers
  • (6aR,10aR)-6,6,9-trimethyl-3-hexyl-6a,7,8,9,10,10a-hexahydrobenzo[c]chromen-1-ol
Chemical and physical data
FormulaC22H34O2
Molar mass330.512 g·mol−1
3D model (JSmol)
  • CCCCCCc1cc2OC(C)(C)[C@@H]3CCC(C)C[C@H]3c2c(O)c1
  • InChI=InChI=1S/C22H34O2/c1-5-6-7-8-9-16-13-19(23)21-17-12-15(2)10-11-18(17)22(3,4)24-20(21)14-16/h13-15,17-18,23H,5-12H2,1-4H3/t15?,17-,18-/m1/s1
  • Key:OKXUDFJPZMVBEH-HSFDIDPMSA-N

Hexahydrocannabihexol (HHCH) is a semi-synthetic cannabinoid derivative. It was first synthesised by Roger Adams in 1942 and found to be more potent than either the pentyl or heptyl homologues, or the unsaturated tetrahydrocannabinol analogue.[1][2] HHCH was first identified as a designer drug in Sweden in September 2023.[3]

Legality

[edit]

HHCH is classified as an "intoxicating cannabinoid" in Colorado and requires a license for its manufacture or distribution.[4]

In Japan, after several people who had eaten gummy candies containing HHCH fell ill, this chemical was officially added to the list of designated substances. And since 2 December 2023, it has been illegal to possess, use, or sell it.[5]

See also

[edit]

References

[edit]
  1. ^ Adams R, Loewe S, Smith CM, McPhee WD (March 1942). "Tetrahydrocannabinol homologs and analogs with marihuana activity. XIII". Journal of the American Chemical Society. 64 (3): 694–697. doi:10.1021/ja01255a061.
  2. ^ "Hexahydrocannabinol (HHC) and related substances" (PDF). European Monitoring Centre for Drugs and Drug Addiction. 2023.
  3. ^ "New psychoactive substances - the current situation in Europe" (PDF). European Drug Report. European Union Drugs Agency (EUDA). 2024.
  4. ^ "Senate Bill 23-271" (PDF). General Assembly, State of Colorado.
  5. ^ "Japanese government to ban cannabis-like substance, HHCH". NHK. 2023-11-21. Retrieved 2023-11-22.