Description
Buy 4-CEC Online | Premium Analytical Reagent Supplier
Buy 4-CEC online for Laboratory Research
Looking to secure a reliable supply of 4-CEC for forensic profiling, mass spectrometry calibration, or neuroreceptor transport assays? As a leading European chemical distributor, we deliver certified, premium-grade 4-Chloroethcathinone Crystal synthesized under strict laboratory quality control parameters. When you buy 4-CEC online through our encrypted portal, you receive a highly stable analytical reference
standard optimized for in vitro testing.
We cater exclusively to individuals , corporate entities, academic institutions, and contract research organizations (CROs). Whether you want to buy 4-CEC online or your project requires retail gram quantities or a long-term bulk 4-CEC supplier contract, our logistics network ensures consistent purity across every batch.
Technical Specifications & Product Identification Data
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- Systematic IUPAC Nomenclature: 1-(4-chlorophenyl)-2-(ethylamino)propan-1-one
- Standard CAS Registry Number: 774705-44-3 (Base) | 22198-75-0 (Hydrochloride Salt)
- Molecular Formula: C₁₁H₁₄ClNO · HCl (Refined Hydrochloride Crystal Form)
- Exact Molar Mass: 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 at the para position and an N-ethyl group on the alkyl side chain
Theoretical Pharmacology & Documented Adverse Effects
Before you order 4-CEC crystal, note that in vitro transport assays classify it as a central nervous system stimulant. Mechanistically, it functions as a monoamine reuptake inhibitor. Due to the chlorination at the fourth 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 pronounced autonomic overstimulation. Documented systemic effects include acute tachycardia, peripheral vasoconstriction, elevated blood pressure, severe appetite suppression, hyperthermia, and involuntary muscle tremors. Furthermore, chemical profiling literature warns of potential neurotoxic risks associated with 4-halogenated cathinone exposures if laboratory containment protocols fail.
Legal Status & European Regulations
The international legal framework surrounding halogenated N-ethyl cathinones is zero-tolerance and heavily monitored:
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- European Union: Strictly controlled, scheduled, or blanket-banned across all EU Member States. National frameworks—such as Germany’s NpSG (broad structural group ban) and equivalent controlled substance laws in France, Poland, and Sweden—restrict distribution solely to state-authorized scientific installations.
- United Kingdom: Controlled universally under the Psychoactive Substances Act 2016 (or scheduled directly as a Class B compound under the Misuse of Drugs Act 1971), making unauthorized production, supply, or importation completely illegal.
- 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 4-CEC?
As a potent synthetic cathinone derivative, exposure to 4-CEC carries severe cardiovascular and neurological risks. Documented symptoms include rapid cardiovascular distress (tachycardia and hypertension), metabolic imbalances due to excessive hyperthermia, severe jaw clenching (bruxism), and potential neurotoxicity through monoaminergic pathway disruptions if handling safeguards fail.
How does 4-CEC differ structurally from 4-CMC (4-Chloromethcathinone)?
The molecular structure of 4-CEC differs from 4-CMC by a modification on the amine nitrogen atom. While 4-CMC carries an N-methyl group (-CH₃), 4-CEC features an extended N-ethyl group chain (-CH₂CH₃), which significantly shifts its lipophilicity and clearing behaviors in laboratory tissue models.
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.
