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HS Code |
853332 |
| Name | 2-Quinoxalinone |
| Alternative Names | Quinoxalin-2(1H)-one |
| Molecular Formula | C8H6N2O |
| Molecular Weight | 146.15 g/mol |
| Cas Number | 59-10-9 |
| Appearance | White to yellow crystalline powder |
| Melting Point | 322-325 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.38 g/cm3 |
| Smiles | C1=CC2=NC(=O)N=CC2=C1 |
| Inchi Key | QZAYGJVTTGNDMW-UHFFFAOYSA-N |
As an accredited 2-Quinoxalinone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g bottle of 2-Quinoxalinone comes in a sealed amber glass container with a tight screw cap and hazard labeling. |
| Shipping | 2-Quinoxalinone is typically shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be handled with care, following relevant safety and regulatory guidelines. Transportation must comply with local, national, and international chemical shipping regulations to ensure safety and prevent contamination or accidental release during transit. |
| Storage | 2-Quinoxalinone should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Keep the storage area clearly labeled and restrict access to trained personnel. Follow all relevant safety guidelines and local regulations for chemical storage. |
Applications of 2-Quinoxalinone in Industrial Manufacturing2-Quinoxalinone provides defined functionality as a chemical intermediate in several specialized manufacturing fields. Its application is recognized in core sectors such as pharmaceutical synthesis, dye production, agrochemical formulation, specialty polymer development, and analytical reagent preparation. As the direct factory, we tailor supply to real customer integration needs, helping bridge precise specifications and downstream scale-up requirements. 1. Pharmaceutical Intermediates for Antibacterial Drug SynthesisPharmaceutical producers utilize 2-quinoxalinone as a scaffold molecule to build advanced antibacterials, including fluoroquinolone derivatives. It enters med-chem and commercial synthesis flows during coupling reactions, ring modifications, and stepwise functionalization. Factories must control input ratios tightly, as the material’s reactivity profile impacts final drug yield and purity. Output batches undergo multi-point verification against pharmacopeial impurity limits, batch traceability, and GMP consistency. Customization spans raw input purity, lot-to-lot validation, and supply-chain documentation as required by regulatory authorities in export destinations. Industry compliance standards
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2. Dye Intermediate for Organic Pigments and ColorantsDye and pigment manufacturers employ 2-quinoxalinone in the synthesis of heterocyclic colorants, particularly benzofuroquinoxaline dyes. The compound serves as a condensation partner and core-building block under strictly controlled conditions. Operators tailor temperature, acid/base settings, and oxidant ratios for individual dye formulas. Final pigment lots must meet REACH and EN 71 safety thresholds, especially for items sold into textile, printing, or toy component lines. Factory packaging observes toxicity labeling and batch ID for downstream traceability. Industry compliance standards
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3. Agrochemical Synthesis for Systemic Fungicide ProductionAgrochemical plants utilize 2-quinoxalinone as an active intermediate to assemble certain systemic fungicide actives. It enters the synthetic pathway at the core ring formation or as a derivatizing base, often introduced before chlorination or alkylation steps. Downstream processes rely on high-purity supply and robust impurity control to comply with environmental and safety norms governing farm chemical release. Final formulation requires documented QC lot analysis, residue testing, and alignment with regional pesticide registration guidelines. Industry compliance standards
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4. Specialty Polymer Synthesis for High-Performance MaterialsHigh-performance polymer producers select 2-quinoxalinone to introduce reactive heterocycles into specialty engineering materials. It serves as a monomer or functional additive in polyimide, polyamide, and conjugated polymer backbones, controlling glass transition temperature and end-use durability. Ratios depend on targeted properties like chemical resistance, tensile strength, and processability in final molded or extruded shapes. Factory QC covers raw input testing, reaction completion verification, and adherence to performance certification for demanding applications such as electronics or aerospace parts. Industry compliance standards
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5. Analytical Reagent Synthesis for Chromatography and DetectionLaboratory reagent firms and specialty chemical suppliers introduce 2-quinoxalinone into the manufacture of analytical derivatization reagents. Its structure allows for sensitive detection of aldehydes, ketones, and metal ions in HPLC and spectrophotometric analysis. Input ratio and purity directly impact detection limits and background interference. Compliance demands trace contaminant levels and method-specific validation data for export to regulated labs. Industry compliance standards
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At our facility, we approach the synthesis of 2-Quinoxalinone with practical insight shaped by years of hands-on production experience. It’s not some abstract concept on a spreadsheet; it’s a chemical we work with daily, a core piece of many research and industrial applications. The heart of this compound—a quinoxaline ring featuring an embedded ketone—allows it to fill a range of roles in pharmaceutical development, agrochemical synthesis, dyes, and functional materials.
We understand that quality and consistency matter. For 2-Quinoxalinone, every batch needs to meet strict purity standards because users don’t have time to battle impurities during downstream work. The reliability of each kilo produced tracks directly to the precision of our process controls. We perform in-process analytical checks to ensure minimal contamination from related quinoxaline structures, which would complicate both R&D and scale-up scenarios. This strategy means our product avoids unpredictable results in the lab, so formulation teams and medicinal chemists can focus on novel research instead of troubleshooting.
Our lab teams learned quickly that cutting corners in crystallization or drying procedures creates long-term headaches. Each batch of 2-Quinoxalinone is managed to avoid polymorphic inconsistencies, solvent carryover, or micro-contaminants. Precipitation conditions are tuned for morphologies that handle well in both manual and automated processes. Real-world manufacturing isn’t about following a recipe to the letter, either; it’s about adapting when feedstock shipments show expected minor variations or equipment downtime disrupts the sequence. We train our operators to spot these variables and correct course, so customers downstream see minimal surprises.
The difference this approach makes becomes obvious if you’ve ever tried scaling up quinoxalinone production from a pilot run to commercial kiloton scale. Small variations in temperature, agitation, or solvent ratios have the potential to alter both yield and product behavior. We log and analyze these variations across months and years, adjusting workflows until the standard deviation in purity remains within a single percent point. We know from customer feedback that this degree of care translates directly into fewer failed experiments and more predictable pilot plant outcomes for those building on our material.
You’ll find synthetically produced quinoxalinones advertised in a range of purity grades, packaging sizes, and added-function variants. What truly separates ours begins with in-house synthesis from basic aromatic amine feedstocks, tracked through every stage right up to shipment. We don’t rely on third-party reprocessors. Our base quinoxaline substrates come from tightly controlled suppliers we’ve vetted for consistency and regulatory compliance, keeping variability low.
Some competitors purchase off-the-shelf intermediates and simply repackage, which introduces a real risk of cross-contamination and inconsistent impurity profiles. We run full HPLC and NMR analysis for identity confirmation and quantification of trace-level byproducts. End-users in drug development fields, in particular, report that our batches rarely force them to troubleshoot for residual amines or halogenated side products, which can obscure pharmacological studies. This type of diligent in-house work means fewer delays for customers filing documentation for regulatory approval or method validation.
Our experience with customers spans three continents, including pharmaceutical R&D labs, dye manufacturers, and chemical research institutes. Demand for 2-Quinoxalinone continues to grow as researchers identify new activities and more advanced uses for quinoxaline cores. In the field of new molecule discovery, our product features in early-stage lead compound synthesis. Its carbonyl group offers a hook for substitutions, delivering abundant opportunity for structure-based drug design.
A chemist in a midsize research institute once remarked that switching to our product cut a week from their project’s timeline because the initial condensation step completed cleanly with fewer byproducts, reducing the need for reruns. In pigment research, 2-Quinoxalinone’s stable ring system stands out for brightness and robustness in heat and light exposure trials, outperforming some of the commodity grades floating around the market.
Working in regulatory-driven environments means documentation and traceability are just as important as the physical product. We provide authenticated analysis certificates with every shipment, detailing both spectroscopic fingerprints and quantitatively measured purity figures. That level of traceability ripples through the supply chain, allowing end customers to submit dossiers with confidence and avoid costly reprocessing.
In our day-to-day production, the structure of 2-Quinoxalinone (C8H6N2O, CAS 59-31-4) isn’t just relevant for catalog entries—understanding its reactivity guides everything from reagent choice to waste management. The carbonyl group at position 2 of the quinoxaline ring confers reactivity useful in diverse transformations, while still providing enough aromatic stability for storage and transport. We typically supply the product as an off-white crystalline solid, with typical purity exceeding 99% by HPLC, free from starting material residues.
Moisture sensitivity and solubility properties are frequently asked topics, so we monitor drying rigorously and include storage guidance aimed at minimizing hydrolysis risks. In practice, most clients dissolve the powder directly in polar aprotic solvents. Formulation and handling advice flows from lab experiences—if a customer requests higher particle fineness for automated dispensing, we adapt the granulation step based on their end-use feedback.
The packaging we use is compatible with both manual bench-scale weighing and automated large-scale feeding systems. Backed by real inventory data, we know that breakage, clumping, and static charging in standard jugs can delay operations, so bulk batches ship in sealed foil-lined drums or bottles with anti-static liners. This keeps material flow easy and reduces downtime, especially for customers with high-throughput demands.
The chemical market offers several quinoxaline derivatives, many of which provide similar aromatic stability but lack the specific functional handle offered by the ketone group at position 2. We’ve run side-by-side syntheses using other quinoxaline analogs and consistently found that 2-Quinoxalinone’s carbonyl group enables targeted derivatization, especially for introducing side chains or for cyclization into more complex frameworks.
Feedback from formulation chemists suggests that similar quinoxaline derivatives, particularly those lacking a functional group at the 2-position, tend to react more sluggishly or generate unwanted side products under comparable reaction conditions. That raises costs, wastes time, and can threaten final product registrations due to complex impurity profiles. By starting with 2-Quinoxalinone, our customers streamline their synthesis efforts, increasing yields and reducing chromatographic steps.
For pigment and dye applications, other heterocyclic ketones, such as 2-benzoxazolinone, often fall short on colorfastness or chemical stability. 2-Quinoxalinone’s fused ring and its precise location of the carbonyl improve both depth and resilience of coloration after processing. In household and industrial dye settings, fewer complaints about fading or performance loss have followed the integration of this molecule compared to competitor alternatives.
Real-world chemical development rarely follows a linear or predictable path. Our team has weathered urgent requests for kilo-scale quantities to meet accelerated timelines for clinical trial material, and navigated the unique requirements that each customer brings—whether it’s compliance with revised pharmacopeia standards or integration with green chemistry initiatives. We know that moving from the lab bench to pilot plant can expose minor batch inconsistencies that do not show up on paper. Because we fully control every synthesis step, we can rapidly scale up batches or customize production parameters on short notice.
We frequently work with contract research organizations and process chemists during method transfers. Practical tips learned on our own line—whether adjusting temperature ramps to sharpen precipitation, or tweaking filtration timing to avoid clogging—get shared directly. That collaborative mindset limits delays and costly trial runs, creating conditions for successful scale transfer into the customer’s own environment.
In several regulatory filings, our documented impurity profile for 2-Quinoxalinone proved decisive, helping customers avoid multiple rounds of clarification with auditors. We maintain thorough retention samples so that, in the event of any long-term stability question, we can pull and re-analyze matched reference material. This approach guards against the rare but costly regulatory holdup and helps our partners avoid litigation or claims tied to quality offsets.
Sustainability enters into our manufacturing routines every day, shaped by growing scrutiny from authorities and customers alike. 2-Quinoxalinone’s batch process produces a moderate level of aqueous waste, so our waste stream goes through in-plant treatment and neutralization before external disposal. Over years of process optimization, we’ve cut solvent usage by nearly a third, shifted toward recyclable catalyst systems, and digitized batch tracking to minimize bulk transport waste.
Recent customer requests pointed to a preference for returnable bulk packaging and closed-loop shipping cartons. We tested several approaches, settling on corrosion-resistant, reusable liners that meet both chemical compatibility and regulatory requirements for safe transport. End-to-end monitoring of product stability under field conditions—hot summers, mild winters, unpredictable surface transit—feeds back into our packaging design choices, limiting off-spec returns or customer complaints about caked or degraded material.
Our production floor doesn’t trade in buzzwords or abstract promises. The feedback we receive from real customers—be it a saved week in a synthetic route, a cleaner impurity profile in a regulatory dossier, or simply fewer headaches in storage and handling—plays a bigger role in shaping our approach than marketing trends. Lab bench realities link closely with commercial realities; what works in a 250 mL flask sometimes collapses at 20 L scale unless every step is stress-tested, documented, and repeatable. That’s the standard we aim for, batch after batch.
With 2-Quinoxalinone, downstream innovators gain precise control over functionalization without inheriting the batch variability or side reactions seen with off-brand or supplier-blended material. Because we field requests for both supported and unsupported forms, dry or semi-wet, we’ve learned that direct communication with the end user beats generic product specs every time. Several of our larger clients, after experiencing operational hold-ups with lesser material, switched exclusively to our batches for this reason alone.
As the core of a chemical manufacturer, our role extends behind just filling orders. We take pride in the rigor, accountability, and knowledge that feed into every shipment of 2-Quinoxalinone. Experimental uncertainty plagues enough research and development work—inherit problems from raw material can hobble a project before it begins. Our decades of production, engagement with real users, and readiness to adapt make our 2-Quinoxalinone a trusted option in a crowded marketplace.
If you’re searching for a reliable building block that holds up under scrutiny—not just on a certificate of analysis, but in hands-on use, scale-up, and regulatory submission—our material offers that reliability. The advantages stem less from marketing intent and more from our unbroken chain of hands-on chemical synthesis, batch management, and customer support. Those practical lessons, stacked over time, shape a 2-Quinoxalinone product experienced chemists trust to deliver on its promises, again and again.