Identity and Structure
| Chemical Name | 5-MeO-DiPT |
|---|---|
| Catalog Entity Type | Compound |
| Formula | C17H26N2O |
| Molar Mass | 274.408 g·mol−1 |
| CAS | 4021-34-5 |
| CAS Numbers and Substance Forms | 4021-34-5 |
| Synonyms | 5-OMe-DiPT; 5-Methoxy-N,N-diisopropyltryptamine; Foxy; Foxy Methoxy |
| IUPAC Name | N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-propan-2-ylpropan-2-amine |
| InChI | InChI=1S/C17H26N2O/c1-12(2)19(13(3)4)9-8-14-11-18-17-7-6-15(20-5)10-16(14)17/h6-7,10-13,18H,8-9H2,1-5H3 |
| InChIKey | DNBPMBJFRRVTSJ-UHFFFAOYSA-N |
| SMILES | CC(C)N(C(C)C)CCC1=C[NH]C(C=C2)=C1C=C2OC |
Chemical Identifiers
| PubChem CID | 151182 |
|---|---|
| ChemSpider ID | 133247 |
| DrugBank ID | DB01441 |
| ChEBI ID | CHEBI:48282 |
| KEGG ID | C22724 |
| UNII | 12D06G8W8E |
| CompTox DTXSID | DTXSID00193209 |
Physical Properties
| Melting Point | 181 °C (358 °F) |
|---|
Clinical Data
| Drug Class | Non-selective serotonin receptor agonist; Serotonin 5-HT2A receptor agonist; Serotonergic psychedelic; Hallucinogen; Entactogen; Stimulant |
|---|---|
| Routes of Administration | Oral, others |
Pharmacokinetics
| Onset of Action | 20–30 min or ≤1 hour |
|---|---|
| Duration of Action | 3–6 hours or 4–8 hours |
Legal Status
| Legal Status (Wikipedia Source Text) | BR: Class F2 (Prohibited psychotropics) CA: Unscheduled DE: Anlage I (Authorized scientific use only) UK: Class A US: Schedule I UN: Unscheduled In general Unscheduled and not approved for human consumption, Illegal in Sweden, Denmark, Greece, Japan, Singapore and China |
|---|
Sources and Attribution
| Wikipedia Source URL | https://en.wikipedia.org/?curid=785808 |
|---|---|
| Wikipedia Retrieval Date | 2026-10-21T20:23:08+00:00 |
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