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Phenylpiracetam hydrazide 200mg – 30 capsules

46.00

3 Products -5%
43.70 € /pc
6 Products -10%
41.40 € /pc
8 Products -15%
39.10 € /pc
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Phenylpiracetam Hydrazide (Fonturacetam Hydrazide) 200 mg — 30 oral research capsules. Phenylpiracetam hydrazide is the hydrazide-modified analogue of phenylpiracetam — a clinically registered nootropic developed in the Soviet space program for cosmonaut cognitive enhancement and listed on the WADA prohibited substances list since 2014 due to its measurable performance-enhancing effects in athletic populations. The hydrazide modification (replacement of the carboxamide with a hydrazide group) appears to extend the duration of action and shift the receptor-affinity profile compared with the parent compound, while retaining the characteristic combined cognitive-and-locomotor activation phenotype. The 200 mg per-capsule dose corresponds to the upper tier of clinical-research-equivalent dosing.

RESEARCH USE ONLY  ·  Not for human or veterinary use. For laboratory and collector purposes only.

Purity
≥ 98 % (HPLC) — third-party tested, CoA on file
Form
Research capsules
Content
200 mg Phenylpiracetam Hydrazide per capsule
Total
30 capsules per bottle (6 g total)
Packaging
Sealed bottle with tamper-evident closure
Storage
Room temperature, dry, protected from light
Molecular formula
C₁₂H₁₅N₃O₂
Molecular weight
≈ 233.27 g·mol⁻¹
IUPAC name
2-(4-phenyl-2-oxopyrrolidin-1-yl)acetohydrazide
CAS number
77472-71-0
Synonyms
Fonturacetam hydrazide; phenylpiracetam hydrazide; PPH

Research Overview

Phenylpiracetam (carphedon, fonturacetam) is the phenylated analogue of piracetam — the parent racetam — developed in the Soviet Union in the 1980s and registered as a clinical neuropharmaceutical in Russia for indications including asthenia, post-stroke recovery, and chronic-fatigue syndromes [1]. Its inclusion on the WADA prohibited substances list in 2014 reflects a documented combined cognitive-and-physical-performance-enhancement phenotype not seen with the parent compound — including dopamine reuptake inhibition, increased noradrenergic tone and cold-tolerance enhancement reported in cosmonaut research [1,2]. The hydrazide modification — replacement of the terminal carboxamide nitrogen with a hydrazide — is a structural variation explored in the Russian medicinal-chemistry literature with the goal of optimizing the duration of action and shifting the activity profile [2,3]. In rodent models, phenylpiracetam hydrazide retains the locomotor-activating, anxiolytic and antidepressant-like phenotypes of the parent and displays a longer apparent duration of action; mechanistic work points to dopamine and noradrenaline reuptake modulation in addition to the canonical racetam cholinergic and glutamatergic effects [3]. The compound is widely used as a research tool for studying combined cognitive-and-physical-performance pharmacology.

Primary Research Areas

  • Combined cognitive and physical-performance research — the only racetam with documented evidence of combined cognitive and locomotor activation, of interest in extreme-environment physiology research [1,2].
  • Dopamine and noradrenaline reuptake pharmacology — monoaminergic activity profile distinguishes it from the simpler racetam scaffold and provides a clean tool for catecholamine-system research [2].
  • Cold-tolerance and stress-resilience models — the original cosmonaut-research indication, with documented effects on tolerance to physical and thermal stressors [1].
  • Anti-asthenic and post-stroke recovery models — the parent compound is clinically registered in Russia for these indications; the hydrazide retains the core phenotype [3].
  • Anxiolytic and antidepressant-like research — documented effects in elevated-plus-maze, forced-swim and tail-suspension paradigms [3].

References

  1. Malykh AG, Sadaie MR. Piracetam and piracetam-like drugs: from basic science to novel clinical applications to CNS disorders. Drugs. 2010;70(3):287–312.
  2. Zvejniece L, Svalbe B, Veinberg G, et al. Investigation into stereoselective pharmacological activity of phenotropil. Basic Clin Pharmacol Toxicol. 2011;109(5):407–412.
  3. Firstova YY, Vasil’eva EV, Kovalev GI. Comparative analysis of changes in glutamate and dopamine receptors in mouse brain after a course of administration of nootropics. Neurochem J. 2012;6(4):245–249.

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Limitless BioChem is a trusted supplier of research compounds. Our products meet strict quality standards and are compliant with EU requirements. We focus on the safe and reliable supply of peptides and pure compounds intended exclusively for research or collector purposes.

This product is not intended for human or veterinary use. It is for collection or research purposes only. It cannot be used as food, dietary supplement or medicine! The information provided in the text on this page is for educational purposes only and does not constitute medical or other advice.

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