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1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one(ODQ)

    • Product Name 1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one(ODQ)
    • Alias ODQ
    • Einecs NA-312-833-1
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    647316

    Cas Number 122628-50-6
    Molecular Formula C9H5N3O2
    Molecular Weight 187.16
    Iupac Name 1H-[1,2,4]Oxadiazolo[4,3-a]quinoxalin-1-one
    Synonyms ODQ; NS 2028
    Appearance Yellow powder
    Solubility DMSO, ethanol, and dimethyl formamide
    Melting Point 244-246 °C
    Storage Temperature Store at -20°C
    Pubchem Cid 216297
    Usage Soluble guanylate cyclase inhibitor

    As an accredited 1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one(ODQ) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The packaging contains 1g of 1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one (ODQ) in an amber glass vial, sealed for protection.
    Shipping 1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one (ODQ) is shipped in tightly sealed, chemical-resistant containers to prevent moisture or air exposure. It is transported according to regulations for hazardous laboratory chemicals, with appropriate labeling and documentation, ensuring safe handling, environmental protection, and compliance with international shipping standards.
    Storage Store **1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one (ODQ)** in a tightly sealed container, protected from light and moisture. Keep at 2–8°C (refrigerator), in a cool, dry, and well-ventilated area. Avoid exposure to strong oxidizing agents and sources of ignition. Ensure proper labelling and handle with appropriate personal protective equipment to minimize risk of inhalation or contact.
    Application of 1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one(ODQ)

    Applications of 1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one (ODQ) in Industrial Manufacturing

    1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one (ODQ) serves as a critical intermediate and specialty additive in several advanced industrial sectors. Below we outline the primary downstream application fields where ODQ is integrated into manufacturing, with attention to compliance, technical formulation, plant-level processing, and resulting end products.

    1. Pharmaceutical Active Ingredient Synthesis

    Pharmaceutical manufacturers use ODQ as a selective inhibitor of soluble guanylate cyclase (sGC), a role that is central to synthesizing experimental therapies in cardiovascular and neurodegenerative research pipelines. Production typically involves dedicated GMP suites, where ODQ is precisely dosed in API formation and downstream formulation stages, followed by stringent QC before release into final drug dosage forms.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice
    • US FDA 21 CFR Parts 210 & 211
    • European Pharmacopoeia (monograph reference as intermediate)
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Used at 0.2–3.0% w/w basis in API synthesis; precise ratio depends on the target drug molecule and sGC pathway modulation profile required.
    • Adjustment based on drug substance molar requirements and process yield optimization.

    Downstream process integration

    • Enters at initial API synthesis stage as a pathway modulator.
    • Subject to multi-stage purification, analytical verification, and downstream formulation into solid or injectable forms.
    • Incorporated into cGMP manufacturing lines; residues strictly monitored.

    Final product types

    • Clinical trial oral tablets and capsules targeting vascular function
    • Investigational injectable solutions for neurology studies
    • Cardiovascular research compounds supplied under IND protocols

    2. Biochemical Research Reagent Production

    ODQ is widely adopted in life science research as a selective biochemical tool for in vitro and in vivo signal transduction studies. Reagent manufacturers utilize pharmaceutical-grade ODQ as a reference modulator in signaling assays, producing standardized solutions, powders, and kits for academic, CRO, and pharma lab customers.

    Industry compliance standards

    • ISO 13485:2016 for Medical Device and Diagnostic Reagents
    • ISO 9001:2015 Laboratory Quality Systems
    • REACH registration for EU reagent-grade substance distribution
    • Chemicals Act (Germany) for laboratory supply chain

    Typical usage ratio

    • Formulated at concentrations 1–100 μM in assay preparations or 0.05–0.3% w/v in solution kits.
    • Ratio determined by target assay sensitivity and user protocols.

    Downstream process integration

    • Dissolved or suspended in phosphate-buffered saline or DMSO buffers after release from QC verification.
    • Filled into vials, ampoules, or microplates; distributed for laboratory research use.

    Final product types

    • Standardized sGC inhibition assay kits
    • Ready-to-use liquid and solid research reagents
    • Inhibitor reference panels for signal transduction studies
    • Custom-packaged bulk laboratory supplies

    3. Specialty Fine Chemicals Synthesis

    Fine chemical manufacturers employ ODQ as a building block or intermediate in constructing nitrogen-containing heterocycles and other advanced molecular scaffolds destined for agrochemical, material science, or specialty polymer research sectors. Reactions involving ODQ frequently require high-purity starting material and controlled hydrogenation, cyclization, or halogenation steps.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Fine Chemicals
    • REACH Substance Registration (EC 1907/2006)
    • Hazardous Substance Control (OSHA 29 CFR 1910.1200)
    • Customs and Border Protection Chemical Import/Export Regulations (US)

    Typical usage ratio

    • Dosed at 0.5–5.0 mol% depending on target molecule complexity.
    • Process engineers adjust according to conversion efficiency and side-product minimization.

    Downstream process integration

    • Introduced into batch or semi-continuous reactors as first or second intermediate.
    • Subjected to further transformation (e.g., alkylation, reduction) in multi-step syntheses.
    • Residuals removed via chromatographic or crystallization-based purification train.

    Final product types

    • Agrochemical intermediates for herbicide development
    • Advanced heterocyclic scaffolds for custom synthesis
    • Specialty high-value fine chemical components

    4. Nitric Oxide Signaling Pathway Study Kits

    Manufacturers specializing in cellular pathway analysis supply ODQ as a benchmark sGC inhibitor component in nitric oxide signal transduction kits. These kits, used in pharmaceutical R&D and academic studies, help quantify NO-dependent processes and evaluate drug candidate responses in controlled in vitro or cellular systems.

    Industry compliance standards

    • ISO 13485:2016 for Diagnostic Kits
    • GLP (Good Laboratory Practice, OECD)
    • US Environmental Protection Agency (EPA) Toxic Substances Control Act (for research chemicals)
    • REACH registered for intra-EU kits

    Typical usage ratio

    • Final formulation contains ODQ at concentrations of 10–50 μM per test, stabilized for shipping and user dilution.
    • Batch concentration varies if required for high-throughput or multiplex platforms.

    Downstream process integration

    • Included after raw material purity QC, dissolved into buffered assay solutions.
    • Aseptically filled in final kit configuration (vial, ampule, microplate well).
    • Packaged with other assay components (substrate, buffers, positive/negative controls).

    Final product types

    • Nitric oxide/cGMP cellular pathway assay kits
    • Pharmacological screening panels for investigational drugs
    • Pathway validation kits for high-content screening
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    Certification & Compliance
    More Introduction

    Introducing 1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one (ODQ) — Our Experience With a Key Redox Chemistry Tool

    What We Manufacture

    Our team has focused on producing high-purity 1H-(1,2,4)Oxadiazolo(4,3-a)quinoxalin-1-one, better known as ODQ, for nearly a decade. ODQ stands out in the family of cyclic nitroso compounds. Chemists recognize this molecule for its specific and reliable ability to modulate soluble guanylate cyclase (sGC) in biochemical research. Our batch processes keep the compound free of major impurities, allowing life science researchers to trust their results and build reproducible data sets. Each synthesis run is carefully monitored, and QC is performed using HPLC, NMR, and melting point verification.

    Why ODQ Matters in Research

    Direct knowledge from manufacturing shows that ODQ attracts attention for its selective inhibition of sGC. Unlike broad, nonselective inhibitors, ODQ reacts with the heme group in sGC, blocking its nitric oxide (NO) sensitivity and its ability to convert GTP to cGMP. Scientists use this property to clarify the role of the NO-cGMP signaling pathway in vascular biology, neuroscience, and pharmacology. Without ODQ, distinguishing between sGC-dependent and sGC-independent NO actions would be slow, less clear, or more prone to technical uncertainty.

    New researchers sometimes underestimate the challenges of working with NO signaling tools. ODQ’s selectivity helps establish reliable controls in cell-based and animal systems. In contrast, crude or bulk nitroso compounds often create off-target effects or react nonspecifically with proteins, reducing confidence in data.

    Specifications and Manufacturing Standards

    Successful ODQ manufacturing always comes down to precise control over reagents, solvents, and purification steps. ODQ appears as a yellowish-brown to orange crystalline powder with an assay above 98% by HPLC as standard. Our batches typically reach 99+% purity, and moisture levels fall well below 0.5%. Many published studies note inconsistencies caused by degraded ODQ or mixed isomers, so keeping the product fresh, moisture-free, and free of trace metals really matters. Handling in a dedicated nitrogen atmosphere, with sealed containers and low-temperature storage, preserves both reactivity and appearance. These measures directly affect experimental success in pharmacology and cell biology labs.

    Controlling trace impurities distinguishes high-grade ODQ from commodity powders. Side-products from synthetic steps can act as radical scavengers or colorimetric interferents, undermining experiments. Using analytical spectrometry and parallel sample runs, we ensure our ODQ does not introduce background interference or cytotoxic artifacts.

    Product Models and Quantities

    Our standard model supports most laboratory-scale needs, with 100 mg, 500 mg, and 1 gram vials supplied in amber glass for light sensitivity. Scale-up to larger packages is available, and we have supplied up to 50 gram single lots for drug discovery programs. As a direct manufacturer, we avoid repackaging or secondary handling, so each vial comes freshly weighed, vacuum-sealed, and labeled with synthesis batch and QC documentation. Researchers appreciate knowing their chemical never passed through a third-party repacker, and our logistics team responds quickly to requests for fresh productions or scale adjustments.

    Differences from Other sGC Inhibitors and Analogs

    Chemical literature reports dozens of sGC inhibitors, but few show the mix of selectivity and stability that ODQ offers. For us as makers, two details stand out—the nitroso core’s unique reactivity with heme iron, and its relative stability toward air and light for a molecule of its class. Some analogs, like methylene blue or NS2028, show broader reactivity and react with enzymes or metal centers outside the sGC pathway. Researchers tell us that choosing these broad inhibitors can confuse study outcomes. ODQ’s clean mechanism of action means interpretation remains more straightforward.

    ODQ also handles bench storage and standard lab environments better than many nitroso heterocycles. Large-scale producers often see analogs degrade or oxidize within days, leading to color changes and diminished potency. With ODQ, shelf life under nitrogen at 4°C comfortably reaches two years, and pilot stability tests in ambient conditions still yield more than 90% activity after six months. Our focus on careful packaging and strict environmental control ensures that the batch you open today produces the same results as the batch from last quarter. Academic collaborators often recognize this in the uniformity of their dose-response curves and the smoothness of data between different shipments.

    Applications Built on Practical Experience

    ODQ finds its core use in the study of NO-sGC-cGMP signaling—arguably one of the most important axes in cardiovascular pharmacology. By halting cGMP synthesis downstream of NO, researchers can separate NO-dependent events from parallel pathways like PKG, cAMP, and calcium flux. In our discussions with principal investigators, the most common applications include vascular smooth muscle research, neuronal signaling, platelet aggregation studies, and tumor biology. ODQ’s specificity allows fine mapping of sGC-dependent signaling in knockout mice, smooth muscle strips, and live-cell imaging.

    Working with drug development partners also brings up other practical uses—such as high-throughput screening for cGMP analogs, testing for NO scavenging agents, or preclinical modeling of pulmonary hypertension. Feedback from the field often highlights ODQ’s contribution to data reproducibility, especially in cases where ambiguous results from generic sGC inhibitors used to slow progress.

    Supporting Scientific Progress Through Reliable Supply

    As manufacturers, we hear concerns not just about chemical quality, but also about supply chain interruptions and batch-to-batch consistency. Researchers build experiments based on lead time promises and previous delivery history. Any interruption—whether due to raw material shortage, customs holdups, or unpredictable lead times—directly slows down advances in discovery. Our production schedule prioritizes prompt restocking and direct communication for scheduled re-supply.

    Some chemistries are simple enough that substitutes can slot in without much fuss, but that’s not the case with ODQ. Strict attention to synthetic route yields and purification scale keeps every batch close to the spec. If we see a drift in purity or crystal appearance—even before finished product QC—we halt the line and review recent changes in reagent lots or solvent storage. At least twice each year, QC teams run validation rounds comparing our current product against previous gold-standard reference material. This keeps our supply close to the original literature values published in foundational sGC pathway papers.

    Safety Experience and Responsible Handling

    Direct chemical manufacturing comes with an elevated view of handling risks and safe use. ODQ is not a high-toxicity ingredient, but as a nitroso-containing heterocycle, it deserves respect. Our plant runs continuous air monitoring and containment during synthesis and weighing. Strict labeling, up-to-date SDS documentation, and secondary containment in shipping ensure the compound arrives securely at the user’s bench, free from accidental contamination or deterioration.

    Many mistakes in handling ODQ come from underestimating its photoreactivity or sensitivity to acid/base. We package only from the primary container, never splitting open drums or large bags into smaller lot sizes, as that can introduce static or humidity issues. Customers benefit from full disclosure of the product’s synthetic history and recommended storage protocols. All these safeguards carry over directly into proper laboratory handling, where users benefit from our firsthand safety lessons: avoid opening the vial outside of a fume hood, limit exposure to strong acids, and recap under nitrogen if possible.

    Global Trends and Customer Challenges

    The demand for ODQ rarely comes from only one country or market; discoveries in North America are quickly shared with collaborators in Europe and the Asia-Pacific region. As the manufacturer, we see firsthand the bottlenecks researchers face due to border regulations and changing standards for purity in sensitive biological studies. In one case, regulatory updates in pharmaceutical research meant revisiting every step of drying and pre-shipment packaging. These changes required time and investment, but mistakes here could cost years for a research lab that depends on consistent biochemical tools.

    Every order we fill also brings new problems in logistics and compliance: frozen shipments across hemispheres, navigating customs for research chemicals, or proactively meeting stricter purity checks from regulators. Responding to these conditions isn’t a marketing exercise—each lesson shapes our next production run and storage guideline. We openly share updates with academic and pharmaceutical partners to maintain transparency.

    Responsible Innovation and Future Directions

    Chemical manufacturing companies sometimes get locked into representing only the current need, but repeated conversations with the scientific community encourage us to anticipate future applications and requirements. For ODQ, greener chemistry initiatives set new benchmarks for synthetic route optimization and waste reduction. By switching to less hazardous solvents or improving crystallization efficiency, we expect to reduce both environmental impact and production costs. These refinements aren’t hypothetical—they directly affect throughput, worker safety, and product quality, and they only happen from the inside view of daily chemical production.

    As new analogs of ODQ start to circulate in chemical literature, we keep our focus on classic ODQ synthesis, refining it for higher yields and cleaner crystals. Some early adopters in synthetic medicine request custom derivatives or modified isotopologues for advanced sGC research. Instead of relying solely on batch chemistry, we’ve integrated flow chemistry for select steps, improving trace impurity removal and offering better control over reaction stoichiometry. This approach positions us to respond quickly to changes in research direction or to scale emerging molecules without the delays that plague repackagers or traders.

    Collaborative Feedback Guiding Future Batches

    Chemistry never stops evolving, especially in active research areas like vascular and redox biology. We keep a feedback channel open for users who face practical problems: solubility in new assay buffers, interference in multiplexed assays, or sensitivity to light in long-term animal studies. Many of the improvements in our final product—alternating between glass and polymer-lined cap materials, including single-use nitrogen purge ampoules, or offering additional documentation on trace metal profiling—emerged directly from mid-project discussions with leading scientists.

    In real-world use, modulating ODQ dosing or vehicle solvent can affect outcomes significantly. By providing HPLC and NMR documentation for every batch and offering custom solution preparations on request, we provide a layer of certainty that third-party vendors cannot match. Experience has shown us that this willingness to discuss experimental needs—even before an order—often prevents costly mistakes down the line.

    Conclusion: Chemical Craftsmanship and Scientific Trust

    As a direct manufacturer, our responsibility extends beyond delivering a product that passes analytical tests. ODQ is not merely a packaged substance; it is a reflection of our process discipline, communication with the research community, and openness to solving new problems as they appear. Every successful sGC experiment relies on quality starting materials, and our ongoing dedication to consistency, transparency, and process improvement makes a practical difference in laboratories worldwide.

    ODQ made to strict internal standards has supported thousands of research publications, clinical study designs, and pharmaceutical experiments. This record did not arrive by chance; it comes from careful work, honest communication with end users, and a willingness to re-engineer even seemingly minor steps in synthesis or packaging. As the global research landscape shifts, the demand for trustworthy biochemicals will only intensify. Our role remains clear—use proven experience to support innovation at the bench, one batch at a time.