Identity and Structure
| Chemical Name | 5-MeO-DALT |
|---|---|
| Catalog Entity Type | Compound |
| Formula | C17H22N2O |
| Molar Mass | 270.376 g·mol−1 |
| CAS | 928822-98-4 |
| CAS Numbers and Substance Forms | 928822-98-4 |
| Synonyms | N,N-Diallyl-5-methoxytryptamine; 5-Methoxy-N,N-diallyltryptamine; 5-Methoxy-DALT; Foxtrot |
| IUPAC Name | N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-(prop-2-en-1-yl)prop-2-en-1-amine |
| InChI | InChI=1S/C17H22N2O/c1-4-9-19(10-5-2)11-8-14-13-18-17-7-6-15(20-3)12-16(14)17/h4-7,12-13,18H,1-2,8-11H2,3H3 |
| InChIKey | HGRHWEAUHXYNNP-UHFFFAOYSA-N |
| SMILES | C=CCN(CCC1=CNC2=C1C=C(OC)C=C2)CC=C |
Chemical Identifiers
| PubChem CID | 50878551 |
|---|---|
| ChemSpider ID | 21106245 |
| KEGG ID | C22723 |
| UNII | V25VK0QTAA |
| ChEMBL ID | ChEMBL2391541 |
| CompTox DTXSID | DTXSID30239169 |
Clinical Data
| Drug Class | Serotonin receptor agonist; Serotonergic psychedelic; Hallucinogen |
|---|---|
| Trade Names | Foxtrot |
| Routes of Administration | Oral |
Pharmacokinetics
| Duration of Action | 2–4 hours |
|---|
Legal Status
| Legal Status (Wikipedia Source Text) | BR: Class F2 (Prohibited psychotropics) DE: NpSG (Industrial and scientific use only) UK: Class A UN: Unscheduled. In general unscheduled and not approved for human consumption, Illegal in China, Japan, Singapore, Sweden, Florida and Louisiana |
|---|
Sources and Attribution
| Wikipedia Source URL | https://en.wikipedia.org/?curid=1804802 |
|---|---|
| Wikipedia Retrieval Date | 2026-10-21T19:46:15+00:00 |
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