| Identification | Back Directory | [Name]
N,N-Diallyl-5-methoxytryptamine | [CAS]
928822-98-4 | [Synonyms]
5-MeO-DALT
5-methoxy DALT
5-Methoxy-N,N-dially
N,N-Dially-5-methoxytryptamine
N,N-Diallyl-5-methoxytryptamine
N,N-Diallyl-5-MethoxytryptaMine, GC 95 +%
5-Methoxy-N,N-diallyl-1H-indole-3-ethanamine
5-Methoxy-N,N-di-2-propen-1-yl-1H-indole-3-ethanaMine
5-Methoxy-N,N-diallyl-1H-indole-3-ethanaMine,5-Meo-DALT
1H-Indole-3-ethanamine, 5-methoxy-N,N-di-2-propen-1-yl-
N-allyl-N-(2-(5-methoxy-1H-indol-3-yl)ethyl)prop-2-en-1-amine
N-[2-(5-methoxy-1H-indol-3-yl)ethyl]-N-prop-2-enylprop-2-en-1-amine | [Molecular Formula]
C17H22N2O | [MDL Number]
MFCD11655942 | [MOL File]
928822-98-4.mol | [Molecular Weight]
270.37 |
| Chemical Properties | Back Directory | [Boiling point ]
422.8±45.0 °C(Predicted) | [density ]
1.059 | [solubility ]
DMF: 20 mg/ml; DMF:PBS (pH 7.2) (1:5): 0.15 mg/ml; DMSO: 15 mg/ml; Ethanol: 1.5 mg/ml; Methanol: 1 mg/ml | [form ]
A crystalline solid | [pka]
16.90±0.30(Predicted) |
| Hazard Information | Back Directory | [Uses]
It is a tryptamine derivative recently used as a component in ‘bath salts’ that act directly on monoamine receptors (similar to MDMA) to produce its psychoactive effects. This compound is a standard for the forensic analysis of samples that may contain this compound. | [Uses]
N,N-Diallyl-5-methoxytryptamine is a tryptamine derivative recently used as a component in ‘bath salts’ that act directly on monoamine receptors (similar to MDMA) to produce its psychoactive effects. This compound is a standard for the forensic analysis of samples that may contain this compound.
| [Definition]
ChEBI: 1h-indole-3-ethanamine, 5-methoxy-n,n-di-2-propen-1-yl- is a member of tryptamines. |
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