Anodyne

DMT
Dimethyltryptamine
Molecular structure via molpic based on CDK
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Enable javascript to view conformer structure via 3Dmol.js
Physical properties
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188.27 g/mol [1]
AppearanceCrystals ... also reported as plates from ethanol and light petroleum [1]
Melting point46 °C [1]
Boiling point60-80 °C [1]
DecompositionWhen heated to decomposition if emits toxic fumes of /nitrogen oxides/. [1]
SolubilityFreely soluble in dilute acetic and dilute mineral acids [1]
2.5 [1]
Structural Identifiers
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C12H16N2 [1]
2-(1H-indol-3-yl)-N,N-dimethylethanamine [1]
CN(C)CCC1=CNC2=CC=CC=C21 [1]
InChI=1S/C12H16N2/c1-14(2)8-7-10-9-13-12-6-4-3-5-11(10)12/h3-6,9,13H,7-8H2,1-2H3 [1]
InChIKeyDMULVCHRPCFFGV-UHFFFAOYSA-N [1]
Dosing
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Elimination half-life* Alone: 5 – 15 min * With an monoamine oxidase inhibitor: 1 – 4 hours
Duration of action* Inhalation: ≤30 min * Intravenous: ≤30 min[4] * Intramuscular injection|Intramuscular: 30 – 60 min * Oral administration|Oral with monoamine oxidase inhibitor: 4 – 6 hours

Dimethyltryptamine

Dimethyltryptamine (also known as N,n-dimethyltryptamine, 2-(3-Indolyl)ethyldimethylamine, 3-(2-Dimethylaminoethyl)indole, 1H-Indole-3-ethanamine, N,N-dimethyl-, 2-(1H-Indol-3-yl)-N,N-dimethylethanamine, N,N-dimethyl-1H-Indole-3-ethanamine, 3-[2-(dimethylamino)ethyl]indole, N-dimethyltryptamine, Indole, 3-(2-(dimethylamino)ethyl)- or Indole, 3-[2-(dimethylamino)ethyl]-) is a psychedelic substance of the tryptamine class.

Chemistry

Salts []

Dimethyltryptamine is typically found in the form of its fumarate and hydrochloride salts.

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Dimethyltryptamine is a achiral mixture

Anodyne Usernotes
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0xea / Dimethyltryptamine via ~15mg vaporized produced very light effects but made me leave with newfound meaning and motivation; ~20mg vaporized produced feelings of shooting through space while completely clear in my head, very clean beautiful visuals for 3 minutes; ~25mg vaporized produced feelings of being torn out of my body and lost in space for 3 minutes; ~30mg vaporized made my subconcious start talking "please help me, I want to leave this place(refering to my place in life)"

Experience reports []

Legal status []

  • Australia: Dimethyltryptamine is a S9 substance.
  • Canada: Dimethyltryptamine is a Schedule III substance.
  • United Kingdom: Dimethyltryptamine is a Class A substance.
  • United States: Dimethyltryptamine is a Schedule I under the "Controlled Substances Act (CSA)".
  • Germany: Dimethyltryptamine is a Anlage I substance.
  • Brazil: Dimethyltryptamine is a F2 substance.[3]
  • United Nations: Dimethyltryptamine is a Schedule I drug under the "Convention on Psychotropic Substances 1971".

References []

  1. National Center for Biotechnology Information. PubChem Compound Summary for CID 6089, Dimethyltryptamine. Accessed June 26, 2025. https://pubchem.ncbi.nlm.nih.gov/compound/6089

  2. U.S. Food and Drug Administration; National Center for Advancing Translational Sciences. Dimethyltryptamine. UNII: WUB601BHAA. Global Substance Registration System. Accessed June 26, 2025. https://gsrs.ncats.nih.gov/ginas/app/beta/substances/WUB601BHAA

  3. Anvisa. RDC Nº 804 - Listas de Substâncias Entorpecentes, Psicotrópicas, Precursoras e Outras sob Controle Especial. Diário Oficial da União. July 24, 2023. Accessed June 26, 2025. https://www.in.gov.br/en/web/dou/-/resolucao-rdc-n-804-de-24-de-julho-de-2023-498447451

  4. Barker SA. Administration of N,N-dimethyltryptamine (DMT) in psychedelic therapeutics and research and the study of endogenous DMT. Psychopharmacology (Berl). June 1, 2022; 239(6):1749–1763.