3-FMA – 3-Fluoromethamphetamine Research Chemical
3-FMA,
also known as 3-fluoromethamphetamine, is a fluorinated methamphetamine analogue
with a defined molecular structure and established chemical identifiers. Public
chemical databases identify the compound by the systematic name
1-(3-fluorophenyl)-N-methylpropan-2-amine. Its documented molecular
data make it suitable for structured analytical chemistry and laboratory reference work.
3-FMA Chemical Overview
Chemical Identity
3-FMA
is the common abbreviation for 3-fluoromethamphetamine. The parent compound
is listed under PubChem CID 58216164 and CAS number 1182818-14-9.
Chemical Class
The molecule is a substituted amphetamine-type structure containing a
fluorinated aromatic ring and an N-methyl-substituted amine.
Research Profile
Its defined molecular formula, structural identifiers and database records
provide useful reference points for analytical and chemical research.
3-FMA Specifications
| Common Name | 3-FMA |
| Chemical Name | 3-Fluoromethamphetamine |
| Systematic Name | 1-(3-Fluorophenyl)-N-methylpropan-2-amine |
| CAS Number | 1182818-14-9 |
| PubChem CID | 58216164 |
| Molecular Formula | C10H14FN |
| Molecular Weight | 167.23 g/mol |
| FDA UNII | E5356E50BR |
| InChIKey | RRVAUTPWWWFYQT-UHFFFAOYSA-N |
| SMILES | CC(CC1=CC(=CC=C1)F)NC |
Molecular Structure & Composition
The molecular structure of
3-FMA
contains a fluorinated phenyl ring connected to a propan-2-amine framework
with an N-methyl substituent. The molecular formula is C10H14FN,
corresponding to a molecular weight of 167.23 g/mol.
The documented canonical SMILES is
CC(CC1=CC(=CC=C1)F)NC, while the reported InChIKey is
RRVAUTPWWWFYQT-UHFFFAOYSA-N. These standardized identifiers
can be used to cross-reference the compound across chemical databases.
Analytical & Research Information
Analytical work involving
3-FMA
can use its established CAS, PubChem, UNII, SMILES and InChIKey identifiers
for compound matching, database searches and laboratory documentation.
Public research resources also document analytical differentiation of
regioisomeric fluorinated phenethylamine compounds using techniques such as
chromatographic separation and mass spectrometry. These approaches are useful
when accurate compound identification is required.
Research Applications
Analytical Chemistry
Defined molecular identifiers can support compound identification,
analytical comparison and laboratory record keeping.
Structural Research
The fluorinated aromatic structure provides a defined subject for research
involving substituted amphetamine-type molecular frameworks.
Reference Analysis
CAS, PubChem CID, FDA UNII, SMILES and InChIKey data provide standardized
reference points for chemical database searches.
Professional Research Material
At RCHEMS, product information is presented around clear chemical identification
and professional research reference. For
3-FMA,
the documented molecular information provides a consistent reference for
cataloguing, analytical comparison and laboratory documentation.
Researchers should verify documentation associated with their specific material
and batch before analytical work. Supplier documentation and analytical results
should be considered alongside established chemical database records.
Explore Related Research Chemicals
Researchers exploring fluorinated research compounds can also visit
RC-Kings
for additional chemical reference materials and related research compounds.
Research Use Notice
3-FMA
is presented for laboratory research and analytical reference purposes.
This page provides chemical and scientific information only and does not provide
instructions for human use, dosing or administration.



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