Description
Buy 3-CEC Online | Secured Discrete Delivery EU
Order High-Purity 3-CEC for Laboratory Research
Looking to secure a reliable supply of 3-CEC to buy 3-CEC online for forensic profiling, mass spectrometry calibration, or neuroreceptor transport assays? As a leading European chemical distributor, we deliver certified, premium-grade 3-CEC Crystal synthesized under strict laboratory quality control parameters. When you buy 3-CEC 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 you to buy 3-CEC online for retail gram quantities or a long-term bulk 3-CEC supplier contract, our logistics network ensures consistent purity across every batch
Shipping : We prioritize fast shipping and secure packaging, so your order arrives quickly and confidentially. All orders are packaged in plain, unmarked boxes to ensure your privacy. Additionally, every shipment includes a surprise gift as a token of our appreciation for choosing us
Technical Specifications & Product Identification Data
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- Systematic IUPAC Nomenclature: 1-(3-chlorophenyl)-2-(ethylamino)propan-1-one
- Standard CAS Registry Number: 1049677-54-4 (Base Form)
- Molecular Formula: C₁₁H₁₄ClNO · HCl (Refined Hydrochloride Crystal Form)
- Exact Molar Mass: 211.69 g/mol (Base) | 248.15 g/mol (Refined HCl Salt variant)
- Physical Presentation: Translucent to off-white large crystal structures or dense powder
- Structural Classification: Substituted synthetic cathinone derivative featuring a chlorinated halogen atom substitution at the meta position of the phenyl ring and an N-ethyl group on the alkyl side chain.
Theoretical Pharmacology & Documented Adverse Effects
Before you buy 3-CEC online, note that in vitro transport assays classify it as a potent central nervous system stimulant. Mechanistically, it functions primarily as a monoamine reuptake inhibitor. Due to the presence of the chlorination at the third position of the phenyl ring combined with the N-ethyl modification, it exhibits altered selectivity for serotonin (SERT) and dopamine (DAT) transporters compared to traditional methylated cathinones, acting as a valuable baseline model for halogenated ligand interactions.
Exposure triggers intense physiological overstimulation. Documented systemic effects include acute tachycardia, heavy peripheral vasoconstriction, elevated blood pressure, severe appetite suppression, hyperthermia, and involuntary muscle tremors. Forensic tracking documentation indicates extreme cardiotoxic stress and a pronounced risk of drug-induced psychomotor agitation if standard containment safeguards fail.
Legal Status & European Regulations
The international legal framework surrounding halogenated, extended-chain synthetic cathinone stimulants is strictly enforced and monitored:
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- European Union: Closely monitored by the European Union Drugs Agency (EUDA) and blanket-banned across almost all EU Member States . National laws—such as Germany’s NpSG (broad structural group ban) and equivalent narcotic acts in France and the Netherlands—restrict distribution solely to state-authorized scientific installations holding specialized permits
- United Kingdom:Strictly prohibited under the Psychoactive Substances Act 2016, criminalizing unauthorized production, supply, or importation into British territory.
Authorized Research Use & Safety Warning
The compound 3-CEC is a synthetic substance classified strictly as an analytical reagent or laboratory reference standard. It is not intended for human or veterinary consumption. Ingestion or accidental exposure poses severe, life-threatening health risks and is illegal under various international and national drug control frameworks. 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 3-CEC?
As a potent phenethylamine and substituted cathinone derivative, exposure to 3-CEC carries substantial cardiovascular and neurological risks. Documented adverse reactions include severe hypertensive strain, rapid heart rate (tachycardia), dangerous spikes in core body temperature (hyperthermia), peripheral vasoconstriction, and profound psychomotor agitation. Prolonged exposure or high doses may lead to permanent organ damage or fatality.
How does 3-CEC differ structurally from 4-CEC?
The molecular structure of 3-CEC differs from 4-CEC based on the positioning of the chlorine atom on the aromatic ring. In 3-CEC, the chlorine substitution occurs at the 3rd (meta) position, whereas in 4-CEC, it is at the 4th (para) position. This structural variation significantly alters the compound’s chemical properties, lipophilicity, and its interaction with biological transporters.
Is 3-CEC legal for personal use?
No. In the majority of jurisdictions, including the European Union and the United Kingdom, 3-CEC is a controlled substance. Unauthorized possession, supply, or importation is a criminal offense. Legal access is typically restricted to authorized scientific institutions and requires specific permits for forensic or legitimate research purposes.
