βk-2C-B
| Clinical data | |
|---|---|
| Other names | β-Keto-2C-B; bk-2C-B; 4-Bromo-2,5-dimethoxy-β-ketophenethylamine; 2,5-Dimethoxy-4-bromo-β-ketophenethylamine |
| Routes of administration | Oral, others |
| Drug class | Serotonin receptor modulator; Serotonin 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen |
| Legal status | |
| Legal status |
|
| Pharmacokinetic data | |
| Onset of action | 20–70 minutes |
| Duration of action | 10–40 hours or 10 hours |
| Identifiers | |
| |
| CAS Number | |
| PubChem CID | |
| ChemSpider | |
| UNII | |
| CompTox Dashboard (EPA) | |
| Chemical and physical data | |
| Formula | C10H12BrNO3 |
| Molar mass | 274.111 g/mol (freebase) 310.572 g/mol (HCl salt) g·mol−1 |
| 3D model (JSmol) | |
| |
| |
βk-2C-B, or bk-2C-B, also known as 4-bromo-2,5-dimethoxy-β-ketophenethylamine or as β-keto-2C-B, is a psychedelic drug of the phenethylamine and 2C family. It is the β-keto derivative of 2C-B. The drug is taken orally.
The drug acts as a very-low-potency serotonin 5-HT2A receptor agonist.
βk-2C-B was first described in the scientific literature by Richard Glennon and colleagues in 2004. It was first encountered as a novel designer drug in Europe in 2013. The drug has since become a controlled substance in Canada, Germany, Switzerland, and the United Kingdom.