Chemical Structure
chemicallstructure
Drug Class
Atypical phenylalkylamine / Dopaminergic
Mechanisms of action
DAT inhibition / release
Low SERT/NET activity
Weak TAAR1 interaction possible
Monograph
Chemical Name: Biphenylamphetamine
Development: First synthesized in the 40s.
Structural Interest: Biphenyl substitution increases steric bulk and rigidity. BPMA is probably more fat-soluble due to the lipophilic amine, making it easier to pass the blood-brain barrier-and presenting a faster onset and shorter action.
Modern Interest:The compound is being evaluated for its potential role in dry stimulation - enhanced wakefulness and performance without classic amphetamine euphoria.
Non-euphoric dopaminergics in cognitive and motivational settings. Anorexiant stimulant.

Full Monograph.
Synthesis batch initiated
1 gram target
|Amount acquired for synthesis purposes: 10 g
|Amount acquired for speculative holding: 5 g
Note: These figures reflect total documented acquisitions. Updated manually
OrderBook

Offer

  • 1g x 5 @ 37.70 EUR
  • 100mg x 10 @ 3.00 EUR
  • 100mg x 10 @ 2.50 EUR
  • 100mg x 10 @ 2.05 EUR
  • 100mg x 10 @ 1.85 EUR
  • 100mg x 10 @ 1.50 EUR

Bid

  • 100mg x 50 @ 1.20 EUR
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