Description
Buy NEP Online | Secured Tracked Logistics EU
Order High-Purity NEP for Laboratory Research
Technical Specifications & Product Identification Data
- Systematic IUPAC Nomenclature: (RS)-2-(ethylamino)-1-phenylpentan-1-one
- Standard CAS Registry Number: 18259-89-5 (Base Form) | 244142-94-3 (Hydrochloride Salt Form)
- Molecular Formula: C₁₃H₁₉NO · HCl (Refined Hydrochloride Crystal Form)
- Exact Molar Mass: 205.30 g/mol (Base) | 241.76 g/mol (Refined HCl Salt variant)
- Physical Presentation: Highly stable, translucent to off-white large crystalline structures or compressed crystal blocks
- Structural Classification: Substituted synthetic cathinone derivative featuring an N-ethyl group on the alkyl side chain and a five-carbon backbone (pentedrone core).
Theoretical Pharmacology & Documented Adverse
Effects
Legal Status & European Regulations
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- European Union (EU-Wide Prohibition): Following comprehensive assessments by European health authorities, NEP (N-Ethylpentedrone) is formally scheduled and classified as an illegal drug across all EU Member States [INDEX]. Furthermore, under Delegated Regulation (EU) 2026/314, rigid Category I restrictions apply to the precursor building blocks required for synthesis, completely halting domestic manufacturing within European territory. National frameworks—such as Germany’s NpSG and equivalent narcotic acts in France and the Netherlands—restrict distribution solely to state-authorized installations holding specialized government permits.
- United Kingdom: Controlled rigidly under the Class B framework of the Misuse of Drugs Act 1971 and universally restricted under the Psychoactive Substances Act 2016, criminalizing all forms of unauthorized supply, domestic transfer, or importation into British territory.
- 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 highly potent phenethylamine and substituted cathinone derivative, exposure to NEP carries substantial cardiovascular and neurological risks. Documented adverse reactions include severe hypertensive strain, rapid heart rate (tachycardia), dangerous spikes in core body temperature (hyperthermia), vasoconstriction, and profound psychomotor agitation. Prolonged exposure or high doses may lead to permanent organ damage or severe autonomic nervous system disruptions.
The molecular structure of NEP differs from standard pentedrone solely by the addition on the amine nitrogen. While traditional pentedrone features an N-methyl group (-CH₃), NEP replaces this with an extended N-ethyl group (-CH₂CH₃). This structural variation significantly alters the compound’s lipophilicity, clearance kinetics, and target receptor affinity.
No. In the majority of jurisdictions, including the European Union and the United Kingdom, NEP is a heavily controlled substance. Unauthorized possession, supply, or importation is a criminal offense. Legal access is strictly limited to authorized scientific research institutions and requires specialized permits for forensic or legitimate laboratory research purposes.
