Description
Buy 5-APB Online | Secured Discrete Delivery EU
Order High-Purity 5-APB for Laboratory Research
Looking to secure a reliable supply of 5-APB to buy 5-APB Online for forensic profiling, mass spectrometry calibration, or neuroreceptor transport assays? As a leading European chemical distributor, we deliver certified, premium-grade 5-APB Hydrochloride Crystal synthesized under strict laboratory quality control parameters. When you buy 5-APB online through our encrypted portal, you receive a highly stable analytical reference standard optimized for in vitro testing.
We cater exclusively to everybody, corporate entities, academic institutions, and contract research organizations (CROs). Whether your project requires retail gram quantities or a long-term bulk 5-APB supplier contract, our logistics network ensures consistent purity across every batch.
Technical Specifications & Product Identification Data
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- Systematic IUPAC Nomenclature: 1-(1-benzofuran-5-yl)propan-2-amine
- Standard CAS Registry Number: 286834-84-2 (Base) | 286834-85-3 (Hydrochloride Salt Form)
- Molecular Formula: C₁₁H₁₃NO · HCl (Refined Hydrochloride Crystal Form)
- Exact Molar Mass: 175.23 g/mol (Base) | 211.69 g/mol (Refined HCl Salt variant)
- Physical Presentation: Translucent to off-white large crystal structures or dense powder
- Structural Classification: Benzofuran derivative and structural analogue of MDA and 6-APB, characterized by an intact benzofuran ring with an aminoethyl sidechain bound specifically at the fifth position.
Theoretical Pharmacology & Documented Adverse Effects
Before you buy 5-APB online , note that in vitro transport assays classify it as a potent central nervous system stimulant and entactogen. Mechanistically, it functions primarily as a potent serotonin-norepinephrine-dopamine releasing agent (SNDRA) and reuptake inhibitor. It displays an exceptionally strong binding affinity for serotonin transporters (SERT) alongside classic catecholamine targets, mimicking the monoaminergic profiling curves of traditional entactogenic compounds.
Exposure triggers pronounced physiological overstimulation. Documented systemic effects include acute tachycardia, peripheral vasoconstriction, elevated blood pressure, severe hyperthermia, mydriasis (pupil dilation), and involuntary muscle tension. Forensic tracking documentation indicates heavy cardiotoxic risk due to secondary 5-HT₂B receptor agonist properties, alongside risks of severe psychological overstimulation if handling protocols collapse.
Legal Status & European Regulations
The international legal framework surrounding benzofuran derivatives is zero-tolerance and rigidly monitored:
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- European Union: Blanket-banned or strictly scheduled as an illicit substance across almost all EU Member States. National laws—such as Germany’s BtMG (narcotics list) and equivalent controlled substance acts in France and the Netherlands—restrict distribution solely to state-authorized scientific or medical installations holding specialized government permits.
- United Kingdom: Strictly criminalized as a Class B controlled substance under the Misuse of Drugs Act 1971.
- 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 & Buyer Disclaimer
This compound is prepared, labeled, and shipped exclusively as an analytical reagent and laboratory reference standard. It is strictly prohibited for human consumption or veterinary use. By placing this item into your cart, Please ensure that you check the legality status of any product you purchase on our website as we cannot be held responsible for it.
Frequently Asked Questions (FAQ)
What are the primary health risks associated with 5-APB?
As a highly potent benzofuran derivative, exposure to 5-APB poses critical cardiovascular and neurological risks. Documented adverse reactions include severe hypertensive strain, rapid tachycardia, dangerous core temperature spikes (hyperthermia), and localized vasoconstriction. Furthermore, its affinity for the 5-HT₂B receptor carries a specific risk of cardiac valvulotoxicity if containment barriers fail.
How does 5-APB differ structurally from 6-APB?
The molecular structures are position isomers. While both compounds share an identical benzofuran ring connected to a propan-2-amine alkyl chain, 5-APB features the substitution specifically at the 5th carbon position of the benzofuran ring, whereas 6-APB positions the exact same sidechain at the 6th carbon marker, modifying its interaction kinetics at target transporters.
Can this material be used for consumer testing?
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.
