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4-AcO-DET Facts

Psychedelic; Substituted tryptamine; Serotonin 2A receptor agonist

Description

4-AcO-DET (4-acetoxy-N,N-diethyltryptamine) — also known as ethacetin — is a synthetic psychedelic of the tryptamine class. It is a prodrug structural analog of psilocybin, converted by the body into 4-HO-DET, the active compound.[1] That active compound activates serotonin receptors in the brain, producing the visual and introspective shifts characteristic of classical psychedelics.

Subjective effects include brightened colors, geometry, emotional intensification, time alteration, and ego dissolution. The experience is qualitatively similar to psilocybin but shorter — an emotionally vivid, introspective tryptamine state with strong visual and philosophical dimensions.

4-AcO-DET is not habit-forming and produces no physical dependence.[2] The primary danger is psychological — panic and potential triggering of psychotic episodes in predisposed individuals — compounded by combining with serotonin-raising drugs like MAOIs and tramadol, which can cause dangerous overheating.

Dose and durationby route · individual sensitivity varies

Oral(mg)
Threshold< 5 mgLight10 – 15 mgCommon15 – 20 mgStrong20 – 35 mgHeavy35+ mg

Starts in 20 – 60 minLasts 4 – 7 hoursAfter-effects 2 – 4 hours

Body and dependence

Acute toxicity
Low
Chronic toxicity
Low
Physical dependence
None
Psychological dependence
Negligible
Withdrawal
None recorded
Compulsive redosing
Negligible

Tolerance

Builds
Rapid
Fully resets after
7 days
Carries over to
psilocybin; psilocin; LSD; DMT; mescaline; 4-AcO-DMT

Effectslikely at a common dose

Perception
Music enhancement; Color enhancement; Visual drifting; Color alteration; Brightness alteration; Geometry; Visual breathing; +28 possible, including Visual haze / noise, Spatial disorientation, Vestibular distortion
Body
Pupil dilation; Body high; Body scan awareness; +32 possible, including Insomnia, Nausea, Motor control impairment
Thinking
Thought connectivity; Pattern recognition enhancement; Aesthetic enhancement; Introspection enhancement; Openness enhancement; +30 possible, including Cognitive impairment, Memory suppression, Decision impairment
Feeling
Emotional enhancement; +8 possible, including Emotional lability, Anxiety, Paranoia
Self
none likely · 9 possible, including Derealization, Depersonalization
Time
Time alteration; +3 possible, including Temporal disorientation

Who shouldn't take it

Absolute
Psychotic disorders; Pregnancy and breastfeeding; MAOI therapy; Lithium therapy; Tramadol co-administration
Relative
Cardiovascular disease; Bipolar disorder

Combinations61 recorded

Lethal (1)
MAOIs
Dangerous (17)
Dopamine agonists; Lithium; MDMA, MDA; NRIs; GHB, Baclofen; GHB, GBL; Ibogaine; Ketamine, DXM, PCP; Local anesthetics; MDMA, Amphetamines; NDRIs (Wellbutrin); Psychedelics; Salvia, Ibogaine; SNRIs; SSRIs; Stimulants; Synthetic cannabinoids
Caution (37)
See full page: psychedex.org/substances/4-aco-det
Not graded (6)
Not listed never means safe.

Seek help immediately if

Most difficulty is psychological (intense fear, panic, confusion) and passes with calm support — the signs below mean seek emergency help:

  • Very high body temperature; hot, dry skin
  • Seizures
  • Chest pain; fast or irregular heartbeat
  • Severe muscle rigidity, tremor, or twitching (possible serotonin syndrome)
  • Cold, pale, or blue fingers/toes — severe vasoconstriction (notably NBOMe / DOx)
  • Persistent vomiting; unconsciousness; uncontrollable agitation or risk of self-harm

What to do

  1. Stay calm and reassure — remind them they took a drug and the effect will pass
  2. Move to a calm, quiet, safe space with low light; reduce noise and sensory input
  3. Keep them from harm — they may act on fear or confusion; stay with them, don't leave them alone
  4. Talk them down gently; don't grab or restrain unless they're in danger
  5. For the medical signs above (overheating, seizure, chest pain, vasoconstriction, unresponsive) call emergency services
  6. If overheating, cool the body; be ready to give rescue breaths / CPR

The experience is time-limited and usually resolves with calm reassurance in a safe setting — psychological first aid, not medication. Serious physical harm is uncommon for classic psychedelics (LSD, psilocybin) but real for some potent phenethylamines (NBOMe, DOx), where hyperthermia, seizures, and vasoconstriction warrant emergency care.

988 Suicide & Crisis LifelineFireside Project: 62-FIRESIDE

Version r1 · Not medical advice

References

  1. [1]
    ^Raithatha SA, Hagel JM, Matinkhoo K, Yu L, Press D, Cook SG, et al. (2024) Novel Psilocin Prodrugs with Altered Pharmacological Properties as Candidate Therapies for Treatment-Resistant Anxiety Disorders — Journal of Medicinal Chemistry doi:10.1021/acs.jmedchem.3c01225
  2. [2]
    ^de la Fuente Revenga M, Jaster AM, McGinn J, Silva G, Saha S, Gonzalez-Maeso J (2022) Tolerance and Cross-Tolerance among Psychedelic and Nonpsychedelic 5-HT2A Receptor Agonists in Mice — ACS Chemical Neuroscience doi:10.1021/acschemneuro.2c00170
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