Skip to content
Varieties from the European CatalogueGrown in FranceSlow dryingDispatched within 24 working hours — before noonEU delivery — 24-72 hRight of withdrawal — 14 daysCertificate available — per batch

Semi-synthetic cannabinoid

Status changing

HHCHexahydrocannabinol

Aliases.Hexahydrocannabinol · 9R/9S-HHC

The first semi-synthetic cannabinoid placed under international control (UN 1971-II, 6 Dec 2025).

Updated on

Level of detail

Identifiers

Formula
C₂₁H₃₂O₂
CAS
6692-85-9
PubChem CID
522237
First described
1947 (Adams) · réémergence 2022
Origin
Semi-synthetic

In plain terms

HHC is a saturated cousin of THC created in the laboratory from CBD. More stable than THC, it saw a commercial wave in Europe in 2022 - then was placed under international control in December 2025. It is no longer marketed.

Receptors and activity

  • CB1 (9R)
    Partial agonist
  • CB1 (9S)
    Partial agonist
  • CB2
    Partial agonist
  • Agonist
  • Partial agonist
  • Antagonist
  • Modulator
  • Inverse agonist

Hover over a row for the precise value (Ki, EC50…)

Subjective signature

Hover over an axis to read its definition.

  • Calm
    55
  • Clarity
    40
  • Sleep
    65
  • Appetite
    70
  • High
    80

Editorial estimate, not clinical.

Pharmacology

First synthesised by Roger Adams in 1947 but remaining obscure until its commercial re-emergence in 2022 in European laboratories, HHC became within three years one of the most closely watched cannabinoids in the world. Its structure no longer contains the double bond of THC - it is saturated by hydrogenation, which makes it more stable to heat and light, but does not remove its psychoactive effect. The two epimers (9R)-HHC and (9S)-HHC coexist in commercial products in variable proportions, with different CB1 affinities - this is why titration and batch purity are critical. Listed in Schedule II of the 1971 Convention by decision CND 68/5 of 12 March 2025, in force on 6 December 2025: the first semi-synthetic cannabinoid placed under international control. Phytogrammes no longer markets it since the scheduling came into force.

Route of preparation (chemical process)

Obtained by catalytic hydrogenation of Δ8/Δ9-THC, itself derived from CBD - saturation of the ring double bonds

Structural classification

Class
Semi-synthetic cannabinoid
Origin
Semi-synthetic
Status
Status changing

Structured data

SMILES
CCCCCC1=CC(=C2[C@@H]3CC(CC[C@H]3C(OC2=C1)(C)C)C)O
Formula
C21H32O2
CAS
6692-85-9
PubChem CID
522237
Machine-readable entry (JSON)

LLM ingestion format: a structured superset of the entry (identifiers, binding, versioned legal status). Full corpus.

In the Journal