bk-2C-B Stats & Data
[Cl-].NCC(=O)c1cc(OC)c(Br)cc1OC.[H+]QEGWLXAUBMCGTL-UHFFFAOYSA-NPharmacology
DrugBankHistory & Culture
bk-2C-B was first characterized in the scientific literature in 2004 by pharmacologist Richard Glennon and his research team, who synthesized and studied the compound as part of investigations into phenethylamine structure-activity relationships. The substance remained largely obscure until 2013, when it emerged on European designer drug markets as a novel psychoactive substance. Following its market appearance, bk-2C-B maintained a consistent presence without generating significant enthusiasm or notoriety within the research chemical community. Despite this relatively muted reception, the compound was sampled by a substantial number of users over subsequent years. It was typically distributed in both pressed pill and powder forms. Its availability persisted in the gray market until regulatory measures were implemented across several countries beginning in 2016.
Toxicity
PsychonautWikiThe toxicity and long-term health effects of recreational βk-2C-B use do not seem to have been studied in any scientific context and the exact toxic dose is unknown. This is because Bk-2C-B is a research chemical with very little history of human usage. Anecdotal evidence from people within the psychonaut community who have tried Bk-2C-B suggests that there are no negative health effects attributed to simply trying the substance by itself at low to moderate doses and using it very sparingly (but nothing can be completely guaranteed). [https://www.google.com/ Independent research] should always be done to ensure that a combination of two or more substances is safe before consumption. It is strongly recommended that one use harm reduction practices when using this substance.
Effect Profile
Curated + 31 ReportsStrong visuals, auditory effects, and body load with mild headspace
Tolerance & Pharmacokinetics
drugs.wikiTolerance Decay
Acute tolerance: develops within a single session — the reset numbers above apply after sustained heavy use, not after one binge. Within-session tachyphylaxis usually resets largely overnight.
Experience Report Analysis
ErowidDemographics
Gender Distribution
Age Distribution
Reports Over Time
Effect Analysis
ErowidEffects aggregated from 31 experience reports (31 Erowid)
Effect Sentiment Distribution
Confidence Distribution
Positive Effects 10
Adverse Effects 8
Dose-Response Correlation
How effect frequency changes across dose levels
View data table
| Effect | Heavy (n=12) |
|---|---|
| Visual Distortions | 100.0% |
| Color Enhancement | 83.3% |
| Anxiety | 66.7% |
| Euphoria | 66.7% |
| Empathy | 58.3% |
| Nausea | 58.3% |
| Body High | 58.3% |
| Confusion | 50.0% |
| Music Enhancement | 50.0% |
| Closed-Eye Visuals | 41.7% |
| Open-Eye Visuals | 41.7% |
| Stimulation | 41.7% |
| Auditory Effects | 41.7% |
| Pupil Dilation | 41.7% |
| Focus Enhancement | 33.3% |
Dose–Effect Mapping
Experience ReportsHow reported effects shift across dose tiers, based on 31 experience reports.
Limited tier coverage — most reports fall within the Heavy range. Effects at other dose levels may not be represented.
| Effect | Heavy (n=12) | |
|---|---|---|
| visual distortions | ||
| color enhancement | ||
| anxiety | ||
| euphoria | ||
| empathy | ||
| nausea | ||
| body high | ||
| confusion | ||
| music enhancement | ||
| closed-eye visuals | ||
| open-eye visuals | ||
| stimulation | ||
| auditory effects | ||
| pupil dilation | ||
| focus enhancement | ||
| hospital | ||
| introspection | ||
| tactile enhancement | ||
| sedation | ||
| sweating |
Showing top 20 of 28 effects
Dosage Distribution
Dose distribution from experience reports
Real-World Dose Distribution
62K DosesFrom 60 individual dose entries
Oral (n=51)
Form / Preparation
Most common forms and preparations reported
Body-Weight Dosing
Dose relative to body weight from reports with weight data
Redose Patterns
Redosing behavior across 26 reports
Legal Status
| Country | Status | Notes |
|---|---|---|
| Canada | Controlled substance | Became a controlled substance in October 2016. Possession, production, and distribution are prohibited under Canadian drug scheduling. |
| Germany | Controlled substance | Classified as an illegal controlled substance. Manufacturing, possession, and distribution are prohibited without authorization. |
| Switzerland | Controlled substance | Listed as a controlled substance under Swiss narcotics legislation. Unauthorized possession and distribution are prohibited. |
| United Kingdom | Controlled (Psychoactive Substances Act 2016) | Prohibited under the Psychoactive Substances Act 2016, which broadly bans the production, supply, and importation of psychoactive substances intended for human consumption. Personal possession is not criminalized under this act, but supply-related offenses carry penalties of up to 7 years imprisonment. |