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Calculated reference model · not an experimental or batch-certified structure. All 10 atoms shown.

Model data & sources
  • Heavy atoms only; hydrogens are omitted from the reference display.
  • Source-defined stereochemistry is checked against the calculated coordinates; no energy-minimum, crystal or solution-structure claim is made.
  • Reference molecular species only; batch identity, purity, counterions and excipients are not certified.
Formula
C6H10N2O2
Method
RDKit ETKDGv3 / MMFF94s calculated reference conformer
Made
2026-01-14
Reports
3 on file
Everything shipping from this page today came off this batch. The code is printed on your label, and one certificate covers the whole batch.

Piracetam

Nootropics

Published formats

  • Dry-Fill Capsule 120ct/400mg/48g
  • Powder 50g
What is the difference between these?
Dry-Fill Capsule
Capsules filled with the weighed solid. The label gives the amount in each capsule and the number in the bottle.
Powder
Raw material as a solid. Nothing added and nothing portioned; the stated weight is what is in the container.
Each label gives the amount per unit and the total, so compare the totals rather than the container size.

Supplementary product details from the published catalog, checked 2026-10-07. These reference details do not establish current availability.

Pricing

Pricing and order placement are reserved for reviewed research accounts. Log in or submit an account application to view current product pricing.

Technical Specifications

Batch COA Database ↗
CAS Registry Number7491-74-9
Molecular FormulaC₆H₁₀N₂O₂
Molecular Weight142.16
IUPAC Designation2-(2-Oxopyrrolidin-1-yl)acetamide
Physical FormWhite crystalline powder
Storage RequirementsRefer to product documentation
Other NamesNootropil, Nootropyl, Pyracetam, Normabrain, Gabacet, Pyramem, Ciclofalina
Capsule Concentration400mg x 120ct
Bulk Powder Quantity50g

Identity fields from the published product record, checked 2026-10-07. Reference information is not a batch identity certificate.

Research Overview

Piracetam (2-Oxo-1-pyrrolidineacetamide) Research Standard

Piracetam (2-oxo-1-pyrrolidineacetamide) is a cyclic derivative of the endogenous neurotransmitter GABA and serves as the foundational parent compound of the racetam class. As the archetype for this series, it has been a cornerstone of neuropharmacological research since 1964. Its defining characteristic in scientific literature is its complex, unresolved mechanism of action, which continues to drive investigations into membrane biophysics, neuronal excitability, and mitochondrial bioenergetics. Because it acts as an all-encompassing scaffold for the entire racetam series, it remains a requisite reference standard for structure-activity relationship (SAR) studies.

Physical & Handling Properties

Property Specification
Physical Appearance White crystalline powder

Mechanism of Action & Research Context

Piracetam’s pharmacology remains a subject of active study. It does not function as a direct agonist or antagonist at any single identified receptor, which distinguishes it from more targeted pharmaceutical agents.

  • Membrane Biophysics: Research investigates the compound’s interaction with the phospholipid bilayer, hypothesizing that it modulates neuronal membrane fluidity, which may indirectly influence receptor protein function and cellular signaling efficiency.

  • AMPA Receptor Modulation: Studies have explored the allosteric modulation of AMPA-type glutamate receptors, proposing that piracetam may influence receptor density or sensitivity in specific neuronal populations.

  • Mitochondrial Bioenergetics: Investigations into mitochondrial function suggest that piracetam may influence oxygen and glucose consumption pathways, providing a stable model for studying cellular energy metabolism under stress.

Research Applications

Piracetam is utilized primarily as a standardized reference compound in comparative neuropharmacology and biophysical studies.

Primary fields of in vitro laboratory investigation include:

  • Membrane Biophysics: Mapping the interactions between pyrrolidinone derivatives and phospholipid model systems to understand how chemical structure influences bilayer dynamics.

  • AMPA Receptor Signaling: Using piracetam as a comparative tool in glutamate receptor modulation assays.

  • Mitochondrial Respirometry: Measuring bioenergetic shifts and ATP production efficiency in cellular cultures exposed to varying concentrations of the parent racetam scaffold.

  • Structure–Activity Relationship (SAR) Research: Serving as the definitive control molecule when evaluating the binding affinity or signaling modulation of newer, higher-potency racetam derivatives.

Storage & Handling Guidelines

Store at controlled room temperature. Keep tightly closed.

Storage guidance is a house recommendation. Analytical documentation is per-lot release testing.

References

  • Giurgea C. (1973) "The 'nootropic' approach to the pharmacology of the integrative activity of the brain." Cond. Reflex. 8(2): 108–115.

  • Malykh AG, Sadaie MR. (2010) "Piracetam and piracetam-like drugs: from basic science to novel clinical applications to CNS disorders." Drugs. 70(3): 287–312.

Related Research Compounds

Research Use Disclaimer

Research Use Only Disclaimer: This product is labeled and sold "For Research Use Only - NOT FOR HUMAN CONSUMPTION." It is not a drug, dietary supplement, food, cosmetic, or medical device, and it is not approved by the FDA or any other regulator for human or veterinary use. It is supplied to approved account holders as a research chemical for laboratory use and must be handled in accordance with applicable law.

Certificates of Analysis

Currently shipping from batch KC-PIR-01.

Kimera Chems

Compounds That Survive Scrutiny

Research use only. Not for human or veterinary use.