Description
Buy 5-MeO-DALT Online | Secured Tracked Logistics EU
Order High-Purity 5-MeO-DALT for Laboratory Research
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Technical Specifications & Product Identification Data
- Systematic IUPAC Nomenclature: N-allyl-N-[2-(5-methoxy-1H-indol-3-yl)ethyl]prop-2-en-1-amine
- Standard CAS Registry Number: 927511-90-6 (Base Form) | 1305436-16-1 (Hydrochloride Salt Form)
- Molecular Formula: C₁₇H₂₂N₂O · HCl (Refined Hydrochloride Crystal Form)
- Exact Molar Mass: 270.37 g/mol (Base) | 306.83 g/mol (Refined HCl Salt variant)
- Physical Presentation: Highly stable fine off-white to beige crystal fragments or dense powder matrices
- Structural Classification: Tryptamine derivative featuring a methoxy group attached at the 5th position of the indole ring system and two allyl functional groups bound symmetrically at the amine nitrogen terminal.
Theoretical Pharmacology & Documented Adverse Effects
Legal Status & European Regulations
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- European Union: Strictly scheduled, banned, or monitored by the European Union Drugs Agency (EUDA) across all EU Member States. National drug schedules—such as Germany’s Betäubungsmittelgesetz (BtMG), the Opiumgesetz in the Netherlands, and equivalent generic legislation in France and Scandinavia—restrict distribution solely to state-authorized scientific installations holding specialized ministerial purchase permits.
- United Kingdom: Strictly criminalized as a Class A controlled substance under the Misuse of Drugs Act 1971 due to broad, sweeping tryptamine analogue framework updates.
Authorized Research Use & Safety Warning
Frequently Asked Questions (FAQ)
As an ultra-potent synthetic tryptamine derivative, exposure to 5-MeO-DALT carries high neurological and psychological risks. Documented symptoms following accidental exposure include profound cognitive confusion, sensory overload, metabolic fluctuations driven by hyperthermia, and acute psychological distress if proper handling containment breaks down.
The molecular structure of 5-MeO-DALT is distinguished entirely by its diallyl amine substitution. While compounds like 5-MeO-DMT carry basic methyl groups, 5-MeO-DALT (Diallyltryptamine) incorporates two three-carbon allyl chains (-CH₂-CH=CH₂) attached symmetrically to the terminal nitrogen, significantly altering its lipophilicity and interactions with metabolic enzymes.
No. This compound is synthesized and handled strictly as an analytical reference standard. It is not approved for human or veterinary consumption, and any such application is completely illegal and carries life-threatening health and legal consequences
