2-FMA 2-Fluoromethamphetamine: Advanced Substituted Amphetamine Reference Standards, Fluorinated Reagents & Forensic Profiling UK
The analytical examination of fluorinated organic compounds, substituted amphetamine derivatives, and specialized reference materials across the United Kingdom requires rigorous access to certified, highly purified chemical reagents. Among structural analogues modified with halogen substituents on the aromatic ring, 2-FMA 2-Fluoromethamphetamine (frequently referenced in analytical literature simply as 2 FMA) stands out as a focal point of high-performance chromatography, forensic screening, and academic exploration. For authorized analytical laboratories, specialized testing facilities, and institutional research groups, securing a dependable stock of high-purity reference material ensures reproducible parameters for structural identification and instrumentation calibration.
Engineered strictly for laboratory benchmarking, reference standardization, and quantitative analytical testing, this specialized compound delivers uniform physical properties and exceptional molecular consistency. A common query raised by researchers and catalog observers navigation compliance questions is: is 2-FMA legal in the uk? Under UK legislation, including the Misuse of Drugs Act via its amphetamine analogue provisions, substituted phenethylamines and ring-substituted amphetamines are strictly controlled. Rather than navigating uncertain supply channels or general marketplaces advertising unverified material when attempting a 2 FMA buy or searching for 2 FMA for sale, procuring certified reference stock through licensed institutional channels guarantees absolute adherence to British compliance standards and precise metrics for high-performance liquid chromatography (HPLC) and mass spectrometry.
Pharmacological Benchmarking & Fluorinated Compound Chemistry
Scientifically classified as (RS)-1-(2-Fluorophenyl)-N-methylpropan-2-amine ($\text{C}_{10}\text{H}_{14}\text{FN}$), this substituted amphetamine features a fluorine atom substituted at the ortho position of the phenyl ring. In professional research environments, analytical teams evaluate its structural behavior, lipophilicity modifications, and receptor-binding profiles across monoamine transporter matrices to map comparative retention times and metabolic degradation timelines against standard reference benchmarks.
When structuring analytical comparative studies, researchers frequently benchmark reference standards against historical metrics or cross-examine binding constants with related stimulants. To review peer-reviewed literature examining fluorinated amphetamine analytics, structure-activity relationships, and forensic screening standards, consult this detailed reference guide on fluorinated amphetamine analytics, structure-activity relationships, and forensic screening standards.
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UK Regulatory Framework & Laboratory Protocols
All chemical reagents, synthetic analogues, and specialized reference compounds distributed throughout the United Kingdom are subject to stringent national oversight under consumer protection laws, chemical safety standards, and related legislative schedules. As a potent research chemical reference standard, handling of bulk 2-FMA 2-Fluoromethamphetamine stock must remain strictly confined to accredited laboratories, forensic toxicology units, and authorized institutions conducting non-human analytical research.
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Technical Specifications Table
| Specification Parameter | Technical Standard / Feature Value |
| Product Identifier | 2-FMA 2-Fluoromethamphetamine |
| IUPAC Nomenclature | (RS)-1-(2-Fluorophenyl)-N-methylpropan-2-amine |
| CAS Registry Number | 1017176-48-5 |
| Molecular Formula | $\text{C}_{10}\text{H}_{14}\text{FN}$ |
| Molecular Weight | 167.22 g/mol (Free Base) / 203.7 g/mol (Hydrochloride) |
| Form Factor | High-Purity Crystalline Powder / Analytical Reference Standard |
| Quality Compliance | Strict Non-Human Laboratory Research Use Only |
Recommended Handling & Storage Guidelines
For professional laboratory environments, store the compound in a tightly sealed, moisture-proof container kept in a cool, dark, and well-ventilated area away from direct sunlight, UV exposure, and heat sources. Proper containment preserves sample stability and prevents environmental degradation during long-term reference archiving.









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