Description
Buy MDMB-4en-PINACA engineered to deliver dependable performance in demanding environments. Manufactured using advanced processing techniques and verified through systematic quality checks, it ensures consistency you can trust.
Whether used in laboratory, industrial, or technical settings, it supports operational efficiency and repeatable outcomes. Secure packaging protects product stability during transit, while clear documentation ensures transparency and traceability. Backed by professional service and responsive support, this solution is ideal for organizations that prioritize reliability and long-term value.
Buy MDMB-4en-PINACA
- Chemical Name: (S)-3,3-dimethyl-2-(1-(pent-4-en-1-yl)-1H-indazole-3-carboxamido)butanoic acid
- Chemical Class: Indazole-3-carboxamide derivative
- Pharmacological Category: Synthetic Cannabinoid Receptor Agonist (SCRA)
- Mechanism: MDMB-4en-PINACA binds to cannabinoid receptors (primarily CB1) and activates them with much higher potency and efficacy than Δ9-THC, the principal psychoactive constituent of cannabis. Unlike THC (a partial agonist), many synthetic cannabinoids—including this compound—act as full agonists, which is associated with: Greater psychoactive intensity, Higher toxicity risk, and Increased incidence of severe adverse reactions
Physical Properties
| Property | Description |
|---|---|
| Chemical Name | Methyl 3,3-dimethyl-2-(1-(pent-4-en-1-yl)-1H-indazole-3-carboxamido)butanoate |
| Chemical Class | Indazole-3-carboxamide synthetic cannabinoid |
| Molecular Formula | C20H28N4O3 |
| Molecular Weight | ~372.46 g/mol |
| Appearance | White to off-white crystalline powder |
| Solubility | Soluble in organic solvents (e.g., methanol, acetonitrile, DMSO); low aqueous solubility |
| Melting Point | Reported ~80–85°C (may vary by batch/purity) |
| LogP (predicted) | High lipophilicity (typically >3) |
| Stability | Sensitive to heat, light, and hydrolysis under strong acidic/basic conditions |
Chemical Assay / Analytical Characteristics
| Parameter | Typical Method / Observation |
|---|---|
| Primary Identification | LC–MS/MS (liquid chromatography–tandem mass spectrometry) |
| Alternative Screening | GC–MS (gas chromatography–mass spectrometry) |
| UV Absorption | Indazole chromophore absorbs in UV range (~220–300 nm) |
| Retention Behavior | Strong retention on C18 reversed-phase columns |
| Ionization Mode | Positive electrospray ionization (ESI+) commonly used |
| Base Peak (MS) | Protonated molecular ion [M+H]+ typically observed |
| Fragmentation Pattern | Characteristic cleavage of tert-leucinate ester and indazole amide bond |
| Quantification | External calibration with certified reference standard |
| Purity Determination | HPLC-UV or LC-MS purity profiling |
related product: ADB-Butinaca
Packaging & Export Compliance
Our Packaging follows the international chemical transport safety standard:
- Aluminum moisture-resistant barrier packaging
- Tamper-evident sealing
- Anti-static protective storage
Shipping compliance aligns with regulations from the International Air Transport Association for air freight and International Maritime Organization for sea freight.
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