Buy 5-MAPB Capsules 100mg Online — Analytical and Safety Profile (100 mg Encapsulated Reference Sample)
5‑(2‑Methylaminopropyl)benzofuran, or Buy 5-MAPB Capsules 100mg, is a benzofuran‑based synthetic compound structurally related to MDMA and 5‑APB.
It acts as a monoamine releasing agent in laboratory pharmacology models.
A “100 mg capsule” may refer to a weighed analytical portion prepared under controlled‑substance licence for forensic calibration or toxicology research.
Organic / Inorganic Chemistry
| Property | Data |
|---|---|
| IUPAC Name | 1‑(benzofuran‑5‑yl)‑N‑methylpropan‑2‑amine |
| Formula | C₁₂H₁₇NO |
| Molecular Mass | 191.27 g · mol⁻¹ |
| Functionality | Secondary amine (N‑methyl), benzofuran aromatic ether. |
| Appearance (salt) | White to off‑white powder usually encapsulated for mass balance testing. |
| pKa (amine) | ~ 9.8 |
| Boiling range (freebase) | ≈ 270 °C (decomp.) |
| Solubility | High in polar organic solvents; moderate in water (HCl salt). |
Chemical Biology
- Pharmacological class: Psychoactive entactogen; monoamine releasing agent.
- Mechanism: Reverses transport through 5‑HT, DA, and NE transporters.
- Relative potency: Comparable to MDMA on serotonin release but longer duration in rodent models.
- Metabolism: N‑Demethylation, β‑hydroxylation, and ring oxidation to catecholic intermediates.
- Applications: Used in neurochemical SAR studies and reference toxicology workflows.
- Toxicological note: Potential for acute serotonergic and neurotoxic effects – research use only.
Computational Chemistry
| Descriptor | Predicted (B3LYP/6‑31G*) |
|---|---|
| Dipole moment | 2.7 D |
| HOMO–LUMO gap | 4.9 eV |
| Pred. log P | 2.6 – 2.8 |
| TPSA | 29 Ų |
| Rotatable bonds | 4 |
| Relative stability vs 5‑APB | Higher hydrophobic energy (ΔG ≈ –4.2 kJ/mol). |
| Docking data | SERT binding energy ~ –8.5 kcal mol⁻¹ (model 5HTT crystal). |
Environmental Chemistry
- Degradation: Oxidatively unstable – cleaves benzofuran → phenolic acids.
- Photolysis: Half‑life ~ 16 h in water under UV.
- Biodegradation: Readily biotransformed in activated sludge.
- Partition coeff.: log Kow ≈ 2.7 → limited bioaccumulation.
- Disposal: Collection as chemical waste for incineration; no drain release.
Laboratory Equipment (for Reference or Forensic Analysis)
| Instrument | Use |
|---|---|
| LC‑MS/MS | [M+H]⁺ = 192.1388; transitions 174 → 161 m/z. |
| GC‑MS (EI) | M⁺ = 191; fragments 58, 131. |
| FTIR | Key bands – 1260 cm⁻¹ (C‑O–C), 1520 cm⁻¹ (NHR bend). |
| NMR (¹H) | Aromatic 6.8–7.3 ppm; N‑CH₃ 2.3 ppm. |
| Capsule integrity test | Weighing variability ± 2 %; dissolution testing only for QC — no biological use. |
| Storage | Inert nitrogen atmosphere, ≤ –20 °C, light‑protected, licensed drug vault. |
Consumables
- Analytical reagent‑grade methanol, acetonitrile, formic acid.
- Disposable fused‑silica vials for MS sampling.
- Nitrile gloves, safety glasses, antistatic weighing boats.
- Class A glassware for precise mass measurements.
- DEA/UK Home Office paperwork for Schedule substance tracking.
Regulation & Safety
| Category | Specification |
|---|---|
| Controlled status | Schedule I (USA); Class B (UK); Schedule 9 (Australia). |
| Permitted uses | Analytical, forensic, licensed research only. |
| GHS classification | Acute Toxicity Oral Cat 3; Specific Target Organ Toxicant. |
| Pictograms | ☠️ ⚠️ 🌡️ |
| Hazard codes | H301, H311, H331, H370. |
| PPE requirements | Lab coat, gloves, fume hood, no open handling outside controlled area. |
| Waste disposal | Licensed incineration ≥ 1000 °C with certificate of destruction. |
Chemical Informatics
| Data Field | Value |
|---|---|
| SMILES | CC(CN(C)C1=CC2=COC=C2C=C1) |
| InChIKey | FZCWKPZJYOJDSH‑UHFFFAOYSA‑N |
| CAS Registry | 1354631‑34‑5 (analytical identifier) |
| Mol weight | 191.27 g mol⁻¹ |
| Pred. log P | 2.75 |
| TPSA | 29.5 Ų |
| Rotatable bonds | 4 |
| Applications | Mass spectral libraries, QSAR training sets, chemical fingerprint databases. |
Ethical and Legal Notice
⚠️ Controlled‑Substance Disclaimer
5‑MAPB and its formulations (including capsules) fall under Schedule I/Class B legislation in accordance with the United Nations Convention on Psychotropic Substances (1971).
Manufacture, distribution, or possession without licence is a criminal offence.
These data serve exclusively for licensed laboratory documentation and forensic education—not for promotion or ingestion.
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