6-APB Facts
Stimulant;
Description
6-APB (6-(2-aminopropyl)benzofuran) — also known as Benzofury — is a synthetic empathogen of the phenethylamine class. It works by releasing serotonin, dopamine, and norepinephrine in the brain and by directly activating serotonin receptors.[1]
Subjective effects include empathy enhancement, euphoria, emotional openness, color brightening, and mild visual distortions. The experience occupies a middle ground between MDMA and MDA — a sustained entactogenic warmth with a slow-building, long-lasting psychedelic overlay.
6-APB does not produce physical dependence, and no lethal dose has been established in any species. The defining long-term concern is cardiac: repeated activation of a serotonin receptor on heart valve cells can cause scarring — the same mechanism behind fenfluramine's valve damage.[1][2][3]
Dose and durationby route · individual sensitivity varies
Starts in 30 – 60 minLasts 7 – 10 hoursAfter-effects 6 – 24 hours
Body and dependence
- Acute toxicity
- Moderate
- Chronic toxicity
- Moderate
- Physical dependence
- Low
- Psychological dependence
- Moderate
- Withdrawal
- Mild
- Compulsive redosing
- Low
Tolerance
- Builds
- Moderate
- Fully resets after
- 49 days
- Carries over to
- MDMA;
MDA; 5-APB; serotonin releasing agents; dopaminergic stimulants
Effectslikely at a common dose
- Perception
- Touch enhancement;
Music enhancement; +15 possible, including Visual haze / noise - Body
- Wakefulness;
Stimulation; Pupil dilation; Body high; Body scan awareness; +32 possible, including Excessive sweating, Bruxism, Insomnia - Thinking
- none likely · 33 possible, including Compulsive redosing urge, Memory suppression, Cognitive impairment
- Feeling
- Empathy enhancement;
Emotional enhancement; Euphoria; +9 possible, including Depression, Anhedonia, Anxiety - Self
- Social connection;
+8 possible, including Craving, Derealization - Time
- none likely · 3 possible, including Temporal disorientation
- Transpersonal
- none likely · 1 possible
- Awareness
- none likely · 4 possible
Who shouldn't take it
Combinations61 recorded
Seek help immediately if
- Overheating / very high body temperature — heavy sweating, then hot dry skin (the leading cause of MDMA deaths, worse when dancing in hot venues)
- Muscle rigidity, jaw clenching, tremor, or twitching (possible serotonin syndrome)
- Fast, pounding heartbeat; chest pain
- Agitation, confusion; seizures
- Hyponatremia (water intoxication) — headache, confusion, drowsiness, vomiting, and seizures from drinking too much water
- Nausea/vomiting; collapse or unconsciousness
What to do
- Move them somewhere cool and help them cool down — overheating is the main danger
- Sip water to stay hydrated but DO NOT overdrink — roughly a cup (250 ml) per hour if active; too much water can be deadly (hyponatremia)
- Get them to rest and stop dancing
- For overheating, seizures, chest pain, muscle rigidity/tremor, confusion, or unresponsiveness, call emergency services
- Recovery position if drowsy or vomiting; stay with them
- Be ready to give rescue breaths / CPR
Most resolve with cooling, rest, sensible hydration, and time. The life-threatening dangers are hyperthermia, serotonin syndrome, and hyponatremia (too much water) — each a medical emergency, not something to wait out.
988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE
References
- [1]^abRickli A, Kopf S, Hoener MC, Liechti ME (2015) Pharmacological profile of novel psychoactive benzofurans — British Journal of Pharmacology doi:10.1111/bph.13128
- [2]^Smith SA, Waggoner AD, de las Fuentes L, Davila-Roman VG (2009) Role of serotoninergic pathways in drug-induced valvular heart disease and diagnostic features by echocardiography — Journal of the American Society of Echocardiography doi:10.1016/j.echo.2009.05.002
- [3]^Lam NT, Balachandran K (2015) The mechanobiology of drug-induced cardiac valve disease — Journal of Long-term Effects of Medical Implants PMID:25955005