DMT | |
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Salts [] | |
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Dimethyltryptamine fumarate | |
Dimethyltryptamine hydrochloride | |
Molecular structure via molpic | |
Conformer structure via 3Dmol.js | |
Molecular formula | C12H16N2[1] |
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Molecular mass | 188.27 g/mol[1] |
Appearance | Crystals ... also reported as plates from ethanol and light petroleum[1] |
Predicted LogP | 2.5[1] |
Melting point | 46 °C[1] |
Boiling point | 60-80 °C[1] |
Decomposition | When heated to decomposition if emits toxic fumes of /nitrogen oxides/.[1] |
Solubility | Freely soluble in dilute acetic and dilute mineral acids[1] |
Chirality | achiral[2] |
Identifiers [] | |
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IUPAC name | 2-(1H-indol-3-yl)-N,N-dimethylethanamine[1] |
SMILES | CN(C)CCC1=CNC2=CC=CC=C21[1] |
InChI | 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] |
InChIKey | DMULVCHRPCFFGV-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 * Intramuscular: 30–60 min * 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 substance of the tryptamine class.
Chemistry
Dimethyltryptamine is typically found in the form of its fumarate and hydrochloride salts.
Stereochemistry
Dimethyltryptamine is a achiral mixture
Subjective effects
Legal status
- Canada: Dimethyltryptamine is a Schedule III substance.
- United Kingdom: Dimethyltryptamine is a Class A substance.
- United States: Dimethyltryptamine is a Schedule I substance.
- Germany: Dimethyltryptamine is a Anlage I substance.
- Brazil: Dimethyltryptamine is a F2 substance.
- United Nations: Dimethyltryptamine is a Schedule I, |, bioavailability, =, Very, low, and, inactive, (except, with, an, monoamine, oxidase and inhibitor) drug under the "Convention on Psychotropic Substances 1971".
See also
External links
- Dimethyltryptamine (Wikipedia)
- Dimethyltryptamine (Wikidata)
- Dimethyltryptamine (DrugBank)
- Dimethyltryptamine (PubChem)
- Dimethyltryptamine (ChEMBL)
- Dimethyltryptamine (ChEBI)
- Dimethyltryptamine (Common Chemistry)
- Dimethyltryptamine (HMDB)
- Dimethyltryptamine (KEGG)
- Dimethyltryptamine (UNII)
- Dimethyltryptamine (EPA DSSTox)