N, N-Dimethyltryptamine / DMT Drug Facts
This document, published by the Drug Enforcement Administration (DEA) in December 2022, provides a comprehensive overview of N, N-Dimethyltryptamine (DMT). Introduction N, N-Dimethyltryptamine (DMT) is considered the prototypical indolethylamine hallucinogen. Chemistry DMT shares the tryptamine core structure common to other indolethylamine hallucinogens. Pharmacology Effects of Use Psychological Effects Physiological Effects Licit and Illicit Uses Distribution […]
Clinically Reviewed by Lauren Barry, LMFT, MCAP, QS
Medically Reviewed by Ali Nikbakht, PsyD
Updated on March 16, 2026 — Editorial Policy | Research Policy | Privacy Policy
This document, published by the Drug Enforcement Administration (DEA) in December 2022, provides a comprehensive overview of N, N-Dimethyltryptamine (DMT).
Introduction
N, N-Dimethyltryptamine (DMT) is considered the prototypical indolethylamine hallucinogen.
- Historical Context: Human experience with DMT likely spans several hundred years due to its use in religious practices and rituals.
- Natural Occurrence: It occurs naturally in many plant species and is a component in South American snuffs and brewed concoctions like Ayahuasca.
- Synthetic Production: DMT can also be produced synthetically. It was first synthesized in 1931 by British chemist Richard Manske.
- Legal History: It gained popularity as a drug of abuse in the 1960s and was placed under federal control as a Schedule I substance in 1971 following the passage of the Controlled Substances Act.
Chemistry
DMT shares the tryptamine core structure common to other indolethylamine hallucinogens.
- Chemical Structure: It is formed by substituting two methyl ($CH_3$) groups for the two hydrogen atoms ($H$) on the terminal nitrogen of the ethylamine side chain of tryptamine.
Pharmacology
- Administration: When used alone, DMT is typically snorted, smoked, or injected.
- Oral Bioavailability: Oral bioavailability is very poor unless combined with substances that inhibit its metabolism.
- In Ayahuasca, harmala alkaloids (harmine, harmaline, tetrahydroharmaline) inhibit the enzyme monoamine oxidase.
- This inhibition allows DMT to remain intact long enough to be absorbed and affect brain function.
- Dosage: In clinical studies, intravenous doses between $0.2$ and $0.4$ $mg/kg$ were found to be fully hallucinogenic.
- Duration: The onset of effects is very rapid, typically resolving within 30 to 45 minutes.
Effects of Use
Psychological Effects
- Intense visual hallucinations.
- Depersonalization and auditory distortions.
- Altered sense of time and body image.
Physiological Effects
- Hypertension and increased heart rate.
- Agitation, seizures, and dilated pupils.
- Nystagmus (involuntary, rapid rhythmic eye movement).
- Dizziness and ataxia (muscular incoordination).
- Severe outcomes such as coma and respiratory arrest have been associated with DMT exposure according to AAPCC data.
Licit and Illicit Uses
- Licit Uses: DMT has no approved medical use in the U.S.. Researchers may use it only under a Schedule I research registration approved by both the DEA and the FDA.
- Illicit Uses: It is sought for its intense psychoactive effects and short duration of action, which appeals to those wanting a psychedelic experience without the extended duration of drugs like LSD. It is commonly smoked or consumed in oral brews.
Distribution and Control Status
- Illicit Distribution: DMT is extracted from plant materials or produced in clandestine labs. Internet sales are a significant source of supply in the U.S..
- Reported Identifications: According to the NFLIS-Drug database, forensic laboratory reports of DMT have remained stable:
- 2018: 726 reports
- 2019: 925 reports
- 2020: 892 reports
- 2021: 1,033 reports
- Control Status: DMT remains a Schedule I controlled substance.
Contact Information: Comments or requests for additional information can be directed to the Drug and Chemical Evaluation Section via Fax (571-362-4250), Telephone (571-362-3249), or Email (DPE@dea.gov).