Etiracetam molecular structure

Etiracetam

(CAS 33996-58-6)

Etiracetam is the original racemic base compound from which the widely used antiepileptic levetiracetam was derived. It has been investigated as a nootropic and memory modulator in animal research.

Formula

C₈H₁₄N₂O₂

Category

Racetam / Levetiracetam precursor

Molar Mass

170.21 g/mol

Legal Status

Unscheduled, research only (US/EU)

Chemical Profile

IUPAC Name:Not disclosed
Molecular Formula:C₈H₁₄N₂O₂
Structure:Racemic, aryl-substituted pyrrolidone
PubChem CID:59708
Molar Mass:170.21 g/mol
Chirality:Racemic (levetiracetam is S-enantiomer)
Origin:Early racetam, precursor to levetiracetam

Mechanism of Action

The active stereoisomer levetiracetam is known to modulate synaptic vesicle protein SV2A function. Etiracetam itself displays racetam-typical modulation of neuronal excitability and memory, but has not been as extensively characterized.

Few mechanistic studies; known mainly as precursor to levetiracetam.

Preclinical Evidence

Alleviation of Memory Retrieval Deficits (Animal Model, 1980)

Animal studies have shown that Etiracetam may alleviate memory retrieval deficits.

Precursor to Levetiracetam

Etiracetam is notable for being the direct synthetic precursor of levetiracetam, a globally-used antiepileptic with proven SV2A modulation and extensive clinical history.

Safety & Side Effects

No animal or clinical safety/tolerability data has been published for etiracetam. Human experience is based only on its S-enantiomer, levetiracetam.

Safety profile unknown for the racemate.

Regulatory & Legal Status

US/EU/International

  • Not FDA or EMA approved.
  • Not a scheduled/controlled substance.
  • Sold as a research chemical only.

Note: Etiracetam is not sold or approved for human use.

History

Developed as a nootropic in the 1970s–80s, Etiracetam fell out of use after the active S-enantiomer, levetiracetam, was separated and commercialized for epilepsy.

1980
Animal Memory Study
1990s
Levetiracetam Approved
etiracetam product image

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Benefits

  • Original racetam precursor to levetiracetam
  • Useful in stereoisomeric research
  • Scientific curiosity in racetam pharmacology

Considerations

  • Not used clinically, not for human use
  • No modern safety data
  • Sold for research only
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