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5-methoxy DALT

Item No. 10729

Product Insert (PDF)GC-MS (PDF)Safety Data Sheet (SDS) (PDF)
Synonyms
Synonyms
  • N,N-Diallyl-5-Methoxytryptamine
Technical Information
Formal Name
5-methoxy-N,N-di-2-propen-1-yl-1H-indole-3-ethanamine
CAS Number
928822-98-4
Molecular Formula
C17H22N2O
Formula Weight
270.4
Purity
≥95%
Formulation
A crystalline solid
Solubility(Learn about Variance in Solubility)
DMF: 20 mg/mlDMF:PBS (pH 7.2) (1:5): 0.15 mg/mlDMSO: 15 mg/mlEthanol: 1.5 mg/mlMethanol: 1 mg/ml
λmax
224, 279 nm
SMILES
COC1=CC=C(NC=C2CCN(CC=C)CC=C)C2=C1
InChi Code
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
InChi Key
HGRHWEAUHXYNNP-UHFFFAOYSA-N
Shipping & Storage Information
Storage
-20°C
Shipping
Room temperature in continental US; may vary elsewhere
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    Product Description

    5-methoxy DALT is a tryptamine derivative recently used as a component in 'bath salts' that act directly on monoamine receptors (similar to 3,4-methylenedioxyamphetamine) to produce its psychoactive effects.1 The physiological, neurological, and toxicological actions of 5-methoxy DALT have not been fully characterized. This compound is intended as an analytical standard for the forensic analysis of samples that may contain this compound.

    WARNING This product is not for human or veterinary use.

    References & Product Citations
    Product Description References

    1. Nonaka, R., Nagai, F., Ogata, A., et al. In vitro screening of psychoactive drugs by [35S]GTPγS binding in rat brain membranes. Biol. Pharm. Bull. 30(12), 2328-2333 (2007).

    Product Citations

    Kozell, L.B., Eshleman, A.J., Swanson, T.L., et al. Pharmacologic activity of substituted tryptamines at 5-HT2AR, 5-HT2CR, 5-HT1AR, and SERT. J. Pharmacol. Exp. Ther. JPET-AR-2022-001454 (2023).