4-FMA Crystal for sale online

Description

4-FMA Crystal – Fluorinated Amphetamine Research Compound | Stacey Chem Sales

The 4-FMA Crystal category at Stacey Chem Sales provides an overview of fluorinated amphetamine research compounds widely referenced in scientific, analytical, and forensic environments. Also known as 4-FMA, 4-fluoromethamphetamine, para-fluoromethamphetamine, or fluorinated methamphetamine analog, this compound belongs to the broader class of substituted amphetamines and phenethylamines.

4-FMA is a laboratory-synthesized compound structurally related to methamphetamine, modified with a fluorine substitution on the aromatic ring. Compounds in this category are typically studied in controlled settings to understand chemical structure, receptor interactions, and analytical detection methods.

At Stacey Chem Sales, we focus on delivering research-oriented information and high-quality laboratory-grade compounds, supporting professionals in analytical and scientific fields.

Product information .4-FMA Crystal for sale online

IUPAC-name      (RS)-1-(4-Fluorophenyl)-N-methylpropan-2-amine

Synonyms         4-Fluoromephamphetamine

Cas number       1246816-62-5

Purity                 98.0 % min.

Appearance       Off-white crystal

What Is 4-FMA?

4-FMA (4-fluoromethamphetamine) is a synthetic phenethylamine and amphetamine derivative characterized by its fluorinated structure. It is also commonly described using synonymous and SEO-relevant keywords such as:

• 4-FMA research chemical
• Para-fluoromethamphetamine (PFMA)
• Fluorinated methamphetamine analog
• Substituted amphetamine compound
• Synthetic CNS-active stimulant
• Phenethylamine derivative
• Laboratory research stimulant

These terms are frequently used in scientific literature, toxicology reports, and analytical chemistry contexts.

Chemical Structure and Properties

4-FMA is chemically identified as a fluorinated derivative of methamphetamine, featuring a phenethylamine backbone with a fluorine atom attached to the aromatic ring.

Key characteristics include:

• Amphetamine and phenethylamine structure
• Fluorine substitution (para-position)
• Laboratory-synthesized compound
• Typically observed in crystalline or powder form

Such structural modifications are important in structure-activity relationship (SAR) studies, helping researchers analyze how chemical changes influence biological activity.