Description
Buy 4-MEC Online | Premium Analytical Reagent Supplier
Order High-Purity 4-MEC for Laboratory Research
Looking to secure a reliable supply or to buy 4-MEC online for forensic profiling, mass spectrometry calibration, or neuroreceptor transport assays? As a leading European chemical distributor, we deliver certified, premium-grade 4-Methylethcathinone Crystal synthesized under strict laboratory quality control parameters. When you buy 4-MEC online through our encrypted portal, you receive a highly stable analytical reference standard optimized for in vitro testing.
We cater exclusively to all clients, corporate entities, academic institutions, and contract research organizations (CROs). Whether you want to buy 4-MEC online for a project that requires retail gram quantities or a long-term bulk 4-MEC supplier contract, our logistics network ensures consistent purity across every batch.
Technical Specifications & Product Identification Data
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- Systematic IUPAC Nomenclature: (R/S)-2-Ethylamino-1-(4-methylphenyl)propan-1-one
- Standard CAS Registry Number: 1225617-18-4 (Base) | 1266688-86-1 (Hydrochloride Salt)
- Molecular Formula: C₁₂H₁₇NO · HCl (Refined Hydrochloride Crystal Form)
- Exact Molar Mass: 227.73 g/mol (Refined HCl Salt variant)
- Physical Presentation: Translucent to off-white large crystal structures or dense powder
- Structural Classification: Synthetic cathinone derivative and close structural homologue of mephedrone (4-MMC)
Theoretical Pharmacology & Documented Adverse Effects
Before you buy 4-MEC online, note that in vitro transport assays classify it as a potent central nervous system stimulant and entactogen. Mechanistically, it functions as a serotonin-norepinephrine-dopamine reuptake inhibitor (SNDRI) and releasing agent. It elevates extracellular neurotransmitter levels similarly to mephedrone but often displays a modified serotonin-to-dopamine ratio during evaluation.
Exposure triggers pronounced autonomic overstimulation. Documented systemic effects include acute tachycardia (heart palpitations), severe peripheral vasoconstriction, elevated blood pressure, hyperthermia (excessive sweating), acute nausea, and heavy jaw clenching (bruxism). Inadvertent absorption poses acute psychostimulant overstimulation risks.
Legal Status & European Regulations
The international legal framework surrounding substituted cathinones is zero-tolerance and heavily monitored:
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- International Scheduling: Globally controlled and listed under Schedule II of the United Nations 1971 Convention on Psychotropic Substances.
- European Union: Strictly prohibited or scheduled as an illicit substance across all EU Member States. National frameworks—such as Germany’s NpSG (Anlage II) and corresponding laws in Poland—restrict distribution solely to state-authorized scientific or medical installations holding specialized government licenses.
- 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 discreetly 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 4-MEC?
As a highly potent synthetic cathinone, exposure to 4-MEC carries significant cardiovascular and neurological risks. Documented adverse reactions include severe hypertensive strain, rapid tachycardia, dangerous core temperature spikes (hyperthermia), and profound psychological agitation if strict laboratory containment barriers fail.
How does 4-MEC differ structurally from mephedrone (4-MMC)?
The molecular structure of 4-MEC is a direct structural homologue of mephedrone. While mephedrone features an N-methyl group (-CH₃) on its alkyl side chain, 4-MEC incorporates an extended N-ethyl group (-CH₂CH₃) at that exact same nitrogen position, altering its target lipophilicity and molecular clearance behaviors during comparative assays.
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 medical and legal consequences.
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
