6-APB Capsules 100mg

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Buy 6-APB Capsules 100mg Online – (6‑(2‑Aminopropyl)benzofuran) — Educational & Compliance Reference

Buy 6-APB Capsules 100mg is a benzofuran‑based heterocyclic amine first identified in analytical toxicology during the rise of novel psychoactive substances (NPS) in the early 2010s.
It appears as a hydrochloride salt, sometimes encountered in forensic casework as a powder or pressed capsule form.

⚠️ Important: Any “capsule” appearance is treated as illicit dosage form in regulated jurisdictions.
This description does not imply manufacture, medical use, or sale.

Organic and Inorganic Chemistry

Property	Description
IUPAC name	1‑(benzofuran‑6‑yl)propan‑2‑amine
Formula	C₁₁H₁₃NO
Molar mass	175.23 g · mol⁻¹
Functional groups	Aromatic ring, furan oxygen, secondary amine (–NH–)
Physical form	Crystalline solid; forms HCl salt for analytical reference.
Reactivity	Acid–base behavior typical of amines; susceptible to oxidative deamination.

Chemical Biology

No approved biomedical application.
Academic interest: SAR (Structure–Activity Relationship) and QSAR modelling of monoamine transporter ligands.
Metabolites: O‑desmethyl‑6‑APB, carboxybenzofuran acids.
Toxicology: Associated with sympathomimetic syndrome (elevated blood pressure, tachycardia, hyperthermia).
Enzyme interaction (computational): Binds predominantly via aromatic π‑stacking and cation–π forces.

Computational Chemistry

Simulation Aspect	Observation
Geometry (DFT B3LYP/6‑31G)*	Planar benzofuran ring, amine side chain torsion ≈ 63°.
HOMO–LUMO gap	≈ 4.2 eV → moderately stable electronically.
Dipole moment	2.05 D.
log P (pred)	2.5 — moderate lipophilicity.
Use in AI/QSAR datasets	Benchmark compound for amine transport affinity predictions.

Environmental Chemistry

- Persistence: Resistant aromatic framework; partial photolysis in aqueous UV exposure.
- Degradation: Oxidative processes yield phenolic and quinone products.
- Waste classification: UN 2811 (Toxic solid, organic); EPA hazardous organic compound.
- Treatment: Incineration > 1000 °C with acid gas scrubbing; advanced oxidation possible.

Laboratory Equipment (Forensic Only)

Instrument	Use
LC‑MS/MS	Quantitative determination in biofluids or solids; m/z 176 → 131 transition.
GC‑MS	Confirmatory mass pattern 77, 105 (m/z indices).
FTIR/Raman	Aromatic C=C ~1598 cm⁻¹, furan C–O stretch ~1255 cm⁻¹, amine ~3300 cm⁻¹.
¹H/¹³C NMR	Assign benzofuran and propan‑2‑amine signals.
UV‑Vis	Absorption λₘₐₓ ≈ 275 nm (π→π* transition).

Consumables

- Amber glass vials with PTFE caps.
- HPLC‑grade methanol or acetonitrile.
- Formic acid for mobile‑phase acidification.
- PTFE membrane filters (0.22 µm).
- Analytical balance, calibrated pipettes, protective sample pouches for reference standards.

Regulation & Safety

Category	Information
Legal status	Scheduled substance under UN Convention on Psychotropic Substances; Schedule I (US DEA); Class A (UK).
Permitted use	Accredited forensic and regulatory laboratory research only.
GHS hazards	H301 (Toxic if swallowed), H331 (Toxic if inhaled), H370 (Causes organ damage).
PPE	Laboratory coat, nitrile gloves, respiratory protection (P3 filter), eye protection.
Storage guidelines	Store ≤ –20 °C in locked controlled‑substance cabinet away from oxidizers.

Chemical Informatics

Descriptor	Data
SMILES	`CC(N)CC1=CC2=C(O1)C=CC=C2`
InChIKey	`QWUWCCQZLGKZHM‑UHFFFAOYSA‑N`
Molecular weight	175.23 g mol⁻¹
TPSA	32.3 Å²
Rotatable bonds	2
FAIR data use	LC‑MS reference libraries, forensic mass spectral catalogues, QSAR datasets.

Ethical and Legal Notice

⚠️ Explicit Disclaimer:
“6‑APB capsules 100 mg” or any dosage presentation constitute illicit, unsanctioned forms under chemical‑control law.
The information above is solely for forensic, regulatory, and public‑health documentation.
Manufacturing, possession, or supply of 6‑APB or its analogues outside licensed research is a criminal offence in most jurisdictions.
All laboratories must comply with ISO 17025, GHS, and national controlled‑substance regulations.