Coluracetam Vega Caps 20mg (30 pcs)

€34

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Buy Coluracetam (Vega Caps) 20mg Online — High‑Purity Racetam Reference Standard for Laboratory Research

Overview

Buy Coluracetam (Vega Caps) 20mg is a pyrrolidone‑based racetam derivative structurally classified as an acetamide nootropic analog, featuring a quinolinone skeleton substituted with a dimethylaminoethyl side chain.
The 20 mg Vega Caps formulation provides uniform, research‑grade capsules that contain 20 mg of Coluracetam (≥ 99% HPLC purity), standardized for spectroscopic, chromatographic, and computational reference purposes under laboratory conditions.

⚠️ For analytical and in‑vitro research only. Not for human consumption, therapeutic application, or clinical use.

Chemical Identity

IUPAC Name: N‑(2,3‑dimethyl‑5,6,7,8‑tetrahydro‑1‑oxo‑1H‑benz[g]indol‑3‑yl)‑2‑(dimethylamino)acetamide
Synonyms: Coluracetam; MKC‑231; BAM‑1110
Chemical Class: Racetam / Pyrrolidone / Quinolinone hybrid compound
Molecular Formula: C19H23N3O3
Molecular Weight: 341.40 g/mol
Purity: ≥ 99.0 % (by HPLC / NMR)
Form: 20 mg capsules (Vega Caps)
Appearance: Pale yellow to off‑white powder in two‑piece capsule
Grade: Analytical / laboratory reference standard

Applications Across Chemistry Disciplines

Organic & Inorganic Chemistry

Possesses both amide and tertiary amine groups — ideal for amide hydrolysis kinetics, amide‑to‑acid derivatization, and H‑bond donor/acceptor analysis.
The quinolinone heterocycle serves as a model for studying π–π conjugation, aromatic substitution, and hydrogen bonding in heteroaromatic systems.
Applicable in photochemical and redox mechanism studies due to aromatic C=O chromophore.
In inorganic chemistry, functions as a potential ligand in simulation of transition metal–amide complexes and coordination chemistry studies.

Chemical Biology

Serves as a reference ligand for simulation of neurotransmitter transport analogs (non‑biological models).
Used in enzyme kinetic assays modeling acetylcholine biosynthetic and metabolic pathways (without biological testing).
Applied in lipid membrane partition and diffusion simulations, highlighting amphiphilic and aromatic interactions.
Excellent for pH stability profiling and in‑vitro oxidative degradation pathway mapping studies.

Computational Chemistry

Benchmark molecule for Density Functional Theory (DFT) and MO (Frontier Orbital) calculations involving nitrogen–oxygen conjugation.
Suitable for Molecular Dynamics (MD) simulations assessing conformational flexibility of amide linkages.
Commonly employed in QSAR and QSPR datasets to predict lipophilicity (log P), dipole moment, and solvation energy.
Used in pharmacophore modeling and quantum descriptor generation for racetam analog libraries.

Environmental Chemistry

Model compound for heterocyclic amide persistence and hydrolytic degradation rate studies.
Supports environmental fate analysis of pharmaceutical residues in wastewater and surface waters.
Applicable to photolytic and oxidative aging experiments for advanced oxidation process (AOP) calibration.
Utilized as a trace analytical standard for LC–MS/MS pollutant detection method validation.

Laboratory Equipment & Consumables

Recommended Analytical Instruments

HPLC / LC–MS/MS systems — quantitative purity & retention time analysis
FTIR spectrometer — amide (1650 cm⁻¹) and C=O (1720 cm⁻¹) stretch identification
¹H / ¹³C NMR spectrometer — ring current shift and functional group confirmation
UV–Vis spectrophotometer — absorbance profile (~325 nm n→π* band)
Thermogravimetric Analyzer (TGA) / DSC — stability testing under heat stress

Essential Laboratory Consumables

Analytical grade solvents: methanol, ethanol, acetonitrile, dimethyl sulfoxide
Amber vials with PTFE caps; glove protection (ISO certified nitrile)
Desiccator cabinet for humidity control
Calibrated pipettes and class‑A glassware for pellet or capsule disintegration testing

Regulation & Safety

Regulatory Status

For research and analytical purposes only; not approved as a dietary, nutraceutical, or pharmaceutical product.
Compliance required with REACH, OSHA HazCom, and CLP Regulations.
Verify jurisdictional classification prior to import or laboratory storage.

Hazard Classification (Indicative GHS)

⚠️ Irritant (Category 2)
⚠️ Eye Irritation (Category 2A)
⚠️ Aquatic Chronic Hazard (Category 3)

Safety Precautions

Handle under controlled environments with fume hood ventilation.
Wear appropriate Personal Protective Equipment (PPE): gloves, goggles, lab coat.
Avoid contact with moisture and oxidizing agents.
Dispose of materials via licensed chemical waste services under EPA and REACH protocols.
Product accompanied by Safety Data Sheet (SDS) and Certificate of Analysis (CoA).

Chemical Informatics & Data Integration

Distributed with SMILES, InChI, and InChIKey identifiers for LIMS and cheminformatics databases.
Includes full set of molecular descriptors: molecular mass, TPSA, polarizability, rotatable bonds, H‑bond donor/acceptor count, and log P.
Compatibility with ChemAxon, RDKit, Open Babel, KNIME, and Schrödinger Suite.
Ideal for machine learning (ML) data training on structure–property relationships and QSAR frameworks.
Metadata format supports FAIR data principles for multi‑lab interoperability.