Description
Buy ADB-BUTINACA Online | Secured Tracked Logistics EU
Order High-Purity ADB-BUTINACA for Laboratory Research
Technical Specifications & Product Identification Data
- Systematic IUPAC Nomenclature: N-(1-amino-3,3-dimethyl-1-oxobutand-2-yl)-1-butyl-1H-indazole-3-carboxamide
- Standard CAS Registry Number: 2398509-08-1 (Free Base Form)
- Molecular Formula: C₁₈H₂₆N₄O₂ (Refined Crystalline Form)
- Exact Molar Mass: 330.43 g/mol
- Physical Presentation: Highly stable, fine white to off-white translucent large crystal structures or dense powder mass
- Structural Classification: Indazole-3-carboxamide synthetic cannabinoid derivative and non-classical synthetic agonist featuring a tert-butyl side group.
Theoretical Pharmacology & Documented Adverse Effects
Legal Status & European Regulations
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- European Union (EU-Wide Prohibition): Following rapid risk assessments by the European Union Drugs Agency (EUDA), ADB-BUTINACA is classified as an illicit drug and banned uniformly across all EU Member States. National drug schedules—including Germany’s BtMG (Anlage I) and equivalent strict generic groupings in France and Poland—prohibit distribution outside specialized state-licensed scientific laboratories.
- United Kingdom: Strictly criminalized as a Class B controlled substance under the Misuse of Drugs Act 1971 due to sweeping synthetic cannabinoid core framework legislation.
- Shipping Policy: Orders addressed to private residential zip codes or unauthorized territories will be delivered securely and discretely at you risk and responsibility
Authorized Research Use & Safety Warning
Frequently Asked Questions (FAQ)
As a non-classical synthetic agonist, accidental exposure to ADB-BUTINACA poses critical medical dangers, including myocardial infarction (heart attack), severe generalized seizures, sudden catatonia, and respiratory depression.
ADB-BUTINACA does not share the classic dibenzopyran ring structure of THC. Instead, it features a totally synthetic indazole-3-carboxamide core coupled with a distinct amino-oxobutane tail. This creates an extremely rigid spatial structure that fully activates CB₁ receptor targets at a fraction of the weight required for classic phytocannabinoids.
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.
