[1] The formalin test in vivo was performed on Δ9-THCB in order to reveal possible analgesic and anti-inflammatory properties.

[1] The tetrad test in mice showed a partial agonistic activity of Δ9-THCB toward the CB1 receptor.

[1] THCB has rarely been isolated from cannabis samples,[1][3] but appears to be less commonly present than THC or THCV.

[6] The Δ8 isomer is known as a synthetic cannabinoid under the code name JWH-130,[7] and the ring-opened analogue cannibidibutol (CBDB) is also known.

[citation needed] THCB is not scheduled internationally under the Convention on Psychotropic Substances, but may be controlled under analogue law in some individual jurisdictions as a homologue of THC.