Product Overview

Piracetam (7491-74-9) is a pharmaceutical active substance (API) of the racetam group of compounds.

It is considered to be the first “nootropic” substance. Piracetam is a white crystalline powder.

It readily dissolves in water and also dissolves in some of the chemicals, like chloroform and ethanol.

Piracetam API is a derivative of GABA, but it acts in a way different from GABA by not directly influencing GABA receptors.

Piracetam API is thought to increase cell membrane function and intersynaptic communication between neurons.

This aspect has rendered it a widely studied substance for cognitive and brain health.

Therapeutic Applications

Piracetam (7491-74-9) has been mainly utilized in cognitive and neurological disorders.

Piracetam has been researched for its uses in memory, learning, and brain function.

It is used in the therapy of cognitive decline and dementia.

It enhances learning and memory in some patients by promoting blood supply and the use of oxygen in the brain.

Piracetam is used in stroke rehabilitation and post-traumatic brain injury, where it supports brain metabolism.

As it increases the fluidity of cell membranes, Piracetam has also been studied for neuroprotection.

It stabilizes brain function during stressful situations, such as a lack of oxygen.

Specification Parameters

Packaging & Storage

Piracetam is supplied in 25 kg fiber drums with inner double liners to protect from moisture.

Research and pilot projects provide smaller packs of 1 to 5 kg.

Each container is sealed, tamper-proof, and labeled with product name, batch number, and storage instructions.

Storage 15–25 °C, in a light-protected dry place, is advised.

Store containers tightly closed to prevent contact with humidity.

Store away from heat and strong oxidizers.

Under these conditions of storage, Piracetam is stable for a term of up to 36 months.

Why Choose Us

Actiza Pharma supplies Piracetam (7491-74-9) with a focus on quality, reliability, and safety.

We produce our product in cutting-edge cGMP facilities using validated processes.

We release every batch only when it has passed stringent analytical requirements.

We include a full COA, MSDS, stability data, and impurity profile with every shipment.

Customization is available. Clients may ask for micronized particle size, special packaging, or tighter impurity requirements.

Our technical team also supports method transfer and USP, EP, and JP compliance.