Classification and Structural Lineage within N-2-methoxybenzylphenethylamine (NBOMe) Series
The chemical identity of 25G-NBOMe is defined by its core structure as a phenethylamine (B48288) and its specific place within the broader family of NBOMe compounds.
Phenethylamine Derivative Identity
25G-NBOMe is fundamentally a phenethylamine derivative. The phenethylamine structure consists of a phenyl ring connected to an amino group by a two-carbon chain, a framework shared by many neuroactive compounds. The specific substitutions on this core structure differentiate 25G-NBOMe from other related molecules. The defining feature of the NBOMe series is the addition of an N-(2-methoxybenzyl) group to the nitrogen atom of the phenethylamine backbone. This structural modification significantly influences the compound’s pharmacological profile, particularly its interaction with serotonin (B10506) receptors.
| Property | Value |
|---|---|
| Formal Name | 2,5-dimethoxy-N-[(2-methoxyphenyl)methyl]-3,4-dimethyl-benzeneethanamine, monohydrochloride |
| CAS Number | 1797132-54-7 |
| Molecular Formula | C₂₀H₂₇NO₃ • HCl |
| Formula Weight | 365.9 g/mol |
| Purity | ≥98% |
Relationship to the 2C-X Family and 2C-G Analog
The NBOMe compounds are synthetic derivatives of the 2C-X family of psychedelic phenethylamines. The “2C” designation, an acronym coined by chemist Alexander Shulgin, refers to the two carbon atoms that link the phenyl ring to the amine group. 25G-NBOMe is specifically the N-(2-methoxybenzyl) derivative of 2C-G, also known as 2,5-Dimethoxy-3,4-dimethylphenethylamine. Analytical studies have shown that the fragmentation patterns of 25G-NBOMe under mass spectrometry are analogous to its parent compound, 2C-G. The addition of the N-benzyl moiety to the 2C structure was found to dramatically increase binding affinity at key serotonin receptors.
Be the first to review “NBOMes 1mg”
Related products
Reviews
There are no reviews yet.