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HS Code |
744681 |
| Chemical Name | 6-Cyano-7-nitroquinoxaline-2,3-dione |
| Abbreviation | CNQX |
| Cas Number | 115066-14-3 |
| Molecular Formula | C9H3N5O4 |
| Molecular Weight | 245.16 g/mol |
| Appearance | Yellow powder |
| Solubility | Soluble in DMSO, ethanol |
| Purity | Typically ≥98% |
| Melting Point | 286-290°C (dec.) |
| Storage Temperature | -20°C (desiccated) |
| Iupac Name | 6-cyano-7-nitroquinoxaline-2,3-dione |
| Usage | Selective AMPA/kainate receptor antagonist |
As an accredited 6-Cyano-7-nitroquinoxaline-2,3-dione(CNQX) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | CNQX is packaged in a sealed amber glass vial, labeled clearly, containing 100 mg of yellow-orange crystalline powder for laboratory use. |
| Shipping | 6-Cyano-7-nitroquinoxaline-2,3-dione (CNQX) is shipped in tightly sealed containers, away from light and moisture, at room temperature or as specified by regulations. Transport follows relevant safety guidelines for hazardous chemicals, with appropriate labeling and documentation to ensure safe handling and compliance with local and international shipping laws. |
| Storage | 6-Cyano-7-nitroquinoxaline-2,3-dione (CNQX) should be stored in a tightly sealed container, protected from light and moisture. Keep it at a temperature of -20°C or below, in a dry, well-ventilated area. Avoid exposure to heat, strong acids, and oxidizing agents. Ensure appropriate labeling, and restrict access to trained personnel using suitable personal protective equipment. |
Applications of 6-Cyano-7-nitroquinoxaline-2,3-dione (CNQX) in Industrial ManufacturingAs a direct manufacturer of 6-Cyano-7-nitroquinoxaline-2,3-dione (CNQX), we support specialized sectors that demand high-purity chemical intermediates and functional compounds. The following application scenarios represent major industrial implementations, detailed by compliance, application ratios, integration points, and common end products. 1. Neuroscience Research Chemical SupplyPharmaceutical research organizations and academic institutes apply this raw material as a selective antagonist in neuropharmacology studies, primarily focusing on AMPA and kainate receptors. High purity and traceable batch compliance remain critical for reliable cell and receptor assay results. Researchers specify concentration and vehicle parameters based on study design, typically incorporating the compound during in vitro or ex vivo assay preparations. Resulting work supports compound screening, receptor mapping, and preclinical publication. Industry compliance standards
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2. Electrophysiology Laboratory ReagentsUniversity laboratories and biotech R&D programs incorporate this molecule as a receptor antagonist to isolate synaptic currents and validate neurotransmission mechanisms during patch clamp and voltage clamp experimentation. Stringent batch analysis ensures minimal contamination affecting sensitive electrical recordings. Preparation standards dictate specific buffer compatibility and light-sensitive handling throughout the workflow. End users commonly extract analytical findings or prepare calibration reference solutions for routine laboratory use. Industry compliance standards
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3. Pharmacological Reference Compound FormulationSpecialty pharmaceutical industries and academic chemistry departments require this substrate as a pharmacological standard for ligand receptor selectivity testing, comparator controls, and validation of drug discovery libraries. Material quality must meet documentation requirements, including spectral purity, trace solvent content, and definitive structural analysis. Controlled process input parameters ensure accurate microgram or milligram preparations compatible with comparator use in automated library screens and quality control reference procedures. Typical formulating steps involve solubilization and individual dispensing prior to plate layout or reference curve setup. Industry compliance standards
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4. Preclinical Neurotoxicology StudiesCROs and biopharmaceutical development teams employ this compound in controlled toxicological models to identify CNS side effect profiles and receptor blockade behavior under preclinical study conditions. Test plans require certified batch traceability, purity reporting, and restricted solvent residue. Typical workflow involves pre-dosing within animal model or tissue slice, accompanied by behavioral or electrophysiological endpoint analyses. Accurate dosing and validated stability play a critical role in data integrity for FDA or EMA submission packages. Industry compliance standards
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For decades, our facility has produced specialty quinoxaline derivatives, but few compounds provoke as much interest in neuroscience and pharmaceutical research as 6-Cyano-7-nitroquinoxaline-2,3-dione—commonly known as CNQX. Every lot that leaves our site reflects the hands-on control we hold from raw material selection through to packaging. This oversight matters deeply to us, since each stage impacts the consistency and reliability our clients demand. Major research institutions and industry labs rely on CNQX for accurate, disease-relevant data. Our approach hinges on batch reproducibility, meaning each shipment maintains purity and identity so experimental conclusions stay solid.
CNQX stands as a benchmark tool in glutamatergic research. Its molecular formula, C9H4N4O4, describes the structure, but for our team, the significance runs deeper. The specific blocking action of CNQX on AMPA and kainate receptors offers precision in mapping neurotransmission that few molecules provide. Many researchers started with less selective antagonists—often running into data ambiguities that stall their projects. CNQX changes the landscape, letting laboratories pinpoint synaptic roles and receptor contributions without noise from off-target effects.
Quality at this level doesn’t happen by accident. Across the production line, team members scrutinize raw cyanation agents and nitration safety measures. Each synthesis step builds on accumulated batch data to mitigate deviations. Years of experience inform our purification strategies—no shortcuts, no fillers, no compromise. The crystalline end product achieves greater than 98% purity by HPLC, consistently clearing key impurity thresholds we set above industry minimums.
Researchers looking into excitatory neurotransmission pathways quickly discover the importance of specificity. Early experiments often relied on broader inhibitors like NBQX or GYKI derivatives, but those compounds can fail to clarify overlapping receptor activities. With CNQX, users reliably block AMPA and kainate channels, avoiding interference at NMDA sites. In our own in-house tests, this selectivity reduces experimental noise and improves reproducibility, especially in electrophysiological recordings from brain slices or cultured neurons.
Pharmaceutical screening benefits as well. Companies evaluating new anti-epileptic or neuroprotective candidates turn to CNQX to dial out glutamatergic noise, isolating drug effects that could otherwise get lost in the signal. For these customers, contaminant profiles and long-term stability count every bit as much as nominal purity. Investments in storage equipment matter little if a chemical degrades over time—a lesson we’ve learned through past customer feedback. We now run deep stability testing and can verify that CNQX retains performance metrics throughout recommended storage intervals.
Manufacturing expertise shapes product availability. By controlling the entire CNQX process, from precursor management to final filtration, we adapt supply in line with demand surges from major discoveries or grant cycles. Clients working on high-throughput screening appreciate the peace of mind that comes from our scale—no research interrupted by unexpected backorders or inconsistent batches.
Several quinoxaline-based antagonists circulate through commercial catalogs, each with a unique fit for specific tasks. CNQX often gets compared to NBQX. Both block AMPA/kainate currents, but differences emerge under scrutiny. NBQX features a bromide substituent, conferring distinct pharmacokinetics and making it less soluble in water. We annually field questions from clients switching from NBQX to CNQX when they need finer experimental control or easier compound preparation—differences with real impact during sensitive patch-clamp or slice work.
GYKI 52466 and other allosteric antagonists target slightly different receptor domains, sometimes leading to ambiguous results in pharmacology studies. With CNQX, the competitive antagonist activity ensures well-defined boundaries in receptor mapping. Our production feedback loop often involves researchers who ran initial screens with a range of compounds, only to settle on CNQX for the consistency it brings to neuron culture assays. The compound’s high aqueous solubility, ease of handling, and robust shelf stability distinguish it in both academic and industrial settings. We tune our crystal grain size and lot-to-lot homogeneity specifically to address solubility bottlenecks that researchers encountered in the mid-2000s, when impurities and polymorphs ruined months of work for many neuroscience labs.
Some customers explore the utility of kynurenic acid, DNQX, or other less specific inhibitors. While these might suit certain receptor-blocking surveys, they lack the selectivity and potency that CNQX offers for AMPA/kainate distinction. This technical edge makes CNQX the primary antagonist for detailed postsynaptic studies both in our collaborations and among published studies in peer-reviewed journals.
No research workflow tolerates downtime or uncertainty about a reagent’s identity. Our clients mention this frequently; a single failed experiment wastes weeks. We ship CNQX as a protected crystalline powder in amber glass to shield it from light-triggered degradation. Internal studies confirm that under recommended conditions, the compound remains stable for extended periods. Experienced researchers value lot traceability. That’s why we log batch documentation and retain reference samples for retrospective analysis if required. Years in the business taught us that accountability begins at the lab bench, not in a marketing statement.
Clients often request custom packaging sizes. We accommodate both large-scale projects—in which hundreds of milligrams move through high-volume flow-cytometry screening—and single-use aliquots for microelectrophysiology. Our filling lines, monitored by trained technicians, prevent cross-batch contamination. There’s no compromise, even in low-volume production runs. We inscribe real-time production dates on each package and maintain digital logs, helping researchers comply with grant or regulatory documentation needs.
Analytical rigor underpins every stage. Each batch runs through HPLC and NMR, confirming both purity and identity. Our lab’s fingerprint library allows us to benchmark current material against every historic production lot—an invaluable tool for clients running time-course studies where subtle shifts contaminate longitudinal trends. Any detected impurities prompt immediate process review and re-run if necessary; no substandard lots leave our warehouse. Independent external labs audit our procedures once per quarter, updating us with the latest compliance findings. We incorporate this continuous quality feedback into manufacturing workflows.
Years ago, incoming customers flagged variance in competitor-sourced CNQX—shifts in melting point or inconsistent dissolution rates. These defects introduced noise into their research, making it difficult to reproduce published results. Such reports drove our decision to commit fully to transparent batch documentation and open communication. Today, clients expect purity because we build it in from the start, not through post-synthesis purification alone. This focus parallels the standards laid out by internationally recognized agencies, giving our customers peace of mind when reporting findings or applying for regulatory approval.
New directions in neuropharmacology depend on precision tools. Our decades-long investment in the repeat production of compounds like CNQX helps customers reach conclusions faster and with fewer confounding factors. Several partners have cited our batch records in peer-reviewed papers, attributing reliable antagonist performance as a key variable that improved their assays. Large research consortia often turn to us for annual supply contracts, minimizing the risk of mid-study batch switches.
Emerging fields—like optogenetics, CRISPR-mediated neurogene editing, or real-time microfluidic systems—bring fresh technical demands. Our chemical engineers collaborate directly with researchers to troubleshoot unexpected results, helping bridge the gap between bench chemistry and on-the-ground brain science. A common concern involves rapid compound photolysis under intense imaging, so we work directly with labs to design optimal storage and handling strategies.
Every inquiry from a research group teaches us something new about the evolving needs in neurotransmitter science. Some customers require tailored documentation to meet regulatory filings; others need rapid feedback on custom synthesis requests. Our workforce draws on backgrounds in preparative organic chemistry, process safety, analytical science, and neuroscience—the insight needed to guide product evolution responsively.
Repeat business from respected neuroscience labs reminds us that our detailed approach to CNQX manufacturing builds trust. By publishing select anonymized batch data and opening direct channels between our chemists and customer R&D teams, we foster collaboration that moves research forward. Assessments after every order help us discover new improvements, whether that involves adjusting packaging, sharing stability updates, or incorporating feedback from peer-reviewed citation databases. Ideas from our commercial partners have resulted in process upgrades—delivering improved dissolution, finer particle size, and increased photostability.
The pathway to high-quality CNQX involves more than technical know-how; it requires conscious stewardship. Waste reduction, solvent recycling, and procurement from ethically screened suppliers allow us to lower environmental impact. Our process chemists invest in catalytic routes that cut byproduct burdens, minimizing hazardous output. Regular audits keep us honest—disclosing solvent usage, recycling percentages, and energy draw during each production run.
We designed our facility with a closed-loop air management system to trap nitration vapors and protect technician safety. These efforts avoid emissions that would otherwise harm community health. Feedback from neighbors and local authorities informs our improvement protocol, ensuring safe and sustainable production. Customer interest in eco-certifications nudges us toward even greater transparency.
As new generations of neuroscientists forge ahead, our mission is to keep pace with rising expectations for reliability, transparency, and environmental responsibility. We embrace feedback, measure performance beyond simple purity, and support sustained research progress. Our production records, from raw ingredient sourcing to final shipment, reflect more than technical rigor—they testify to respect for the work our customers do.
By taking direct responsibility for CNQX’s journey from chemical synthesis to research bench, we reinforce the trust that allows scientific discoveries to flourish. Every batch carries the collective experience of a team grounded in both chemical manufacturing and research priorities. We see each order as a shared investment in the next wave of understanding brain function, disease mechanisms, and therapeutic breakthroughs.
We welcome ongoing dialogue with scientists and technicians who stake their reputations on data quality. Our responsibility expands beyond product shipment, extending to long-term storage guidance, real-time troubleshooting, and sharing the insights gained from years in the field. As broader demands reshape scientific research, we remain committed to manufacturing CNQX—without compromise, and always with the user’s end goal in mind.