|
HS Code |
444250 |
| Cas Number | 3531-19-9 |
| Molecular Formula | C7H3N3O4 |
| Molecular Weight | 193.12 |
| Appearance | Yellow crystalline powder |
| Melting Point | 164-167°C |
| Boiling Point | No data (decomposes) |
| Density | 1.62 g/cm³ (estimated) |
| Solubility In Water | Slightly soluble |
| Purity | Typically ≥98% |
| Smiles | C1=CC(=C(C(=C1[N+](=O)[O-])C#N)[N+](=O)[O-]) |
| Refractive Index | No data available |
| Storage Temperature | Store at room temperature |
| Synonyms | 2,6-Dinitrobenzenecarbonitrile |
| Ec Number | 222-534-7 |
As an accredited 2,6-Dinitrobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle labeled "2,6-Dinitrobenzonitrile" features hazard symbols, product details, and secure screw cap packaging. |
| Shipping | 2,6-Dinitrobenzonitrile is shipped as a hazardous chemical under regulated conditions. It should be packaged in tightly sealed containers, clearly labeled, and protected from physical damage. Transportation must comply with local, national, and international guidelines for toxic and environmentally hazardous substances. Appropriate safety documentation must accompany the shipment at all times. |
| Storage | 2,6-Dinitrobenzonitrile should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and reducing agents. Protect from heat, ignition sources, and direct sunlight. Label the container clearly and ensure it is handled only by trained personnel using appropriate protective equipment to prevent inhalation, ingestion, or skin contact. |
Applications of 2,6-Dinitrobenzonitrile in Industrial Manufacturing2,6-Dinitrobenzonitrile serves as a specialized intermediate in high-value industrial synthesis. Its controlled nitration pattern and aromatic nitrile group offer reactivity essential to defined technical processes. Below, we detail core downstream fields where this material integrates into regulated, well-defined applications, listing industrial requirements, processing roles, and end-market product types. 1. Pharmaceutical Intermediate for Anti-Hypertensive AgentsOur facility supplies 2,6-Dinitrobenzonitrile as a key functionalized intermediate in the synthesis of select anti-hypertensive actives. Process engineers utilize it during the route to dihydropyridine calcium channel blockers via stepwise reduction and functional group transformations. This critical building block supports tightly controlled multistage reactions, demanding adherence to GMP guidelines and validated traceability. Our product passes stringent metal trace and residual solvent thresholds, allowing it to enter regulated pharma APIs with compliance documentation delivered per batch. Industry compliance standards
Typical usage ratio
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2. Agrochemical Synthesis – Herbicide PrecursorOur 2,6-Dinitrobenzonitrile integrates in downstream manufacturing of triazine and pyridine herbicides. Formulation R&D teams select the compound for its electron-withdrawing groups, driving targeted nucleophilic substitution when producing pre-emergent herbicide actives. All supplied batches meet global agrochemical residual purity and contain documentation for field application registrations. Production control documents batch traceability from benzonitrile feedstock through nitro-substitution, supporting major crop protection original substances. Industry compliance standards
Typical usage ratio
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3. Colorant and Pigment IntermediateChemical manufacturers use 2,6-Dinitrobenzonitrile for high-performance pigment intermediates fabrication. The well-defined nitro arrangement allows specialized coupling reactions forming azo and phthalocyanine pigment precursors. Quality managers rely on assured purity and correct isomer ratios to deliver strong, fade-resistant color performance. We supply customized technical documentation to support pigment R&D and qualify materials for use in coatings formulated to meet international standards for industrial and consumer finishes. Industry compliance standards
Typical usage ratio
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4. Electronic Chemicals—Liquid Crystal IntermediateLeading LC display material makers incorporate our 2,6-Dinitrobenzonitrile into synthesis steps for aromatic nitrile-based liquid crystal molecules. This intermediate enables precision insertion of polar functional groups under controlled temperature and solvent conditions, essential for stable dielectric performance. Trace impurity control at our site enables consistent electro-optic response in downstream mixtures, supporting defect-free production and compliance with electronics industry expectations. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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In manufacturing, every compound we produce brings behind it a story of hands-on development and the lessons that arise from solving real problems on the shop floor. Our 2,6-Dinitrobenzonitrile stands as a clear example. It came into our lineup because chemists and engineers in pharmaceuticals, dyes, and advanced materials needed a molecule capable of driving highly specific transformations. You can see this compound described by its IUPAC name, 2,6-Dinitrobenzonitrile, or by its more succinct registry numbers. Yet long before numbers appear on a drum, our process engineers are focused on purity, consistency, and making sure each kilogram behaves predictably in the next person’s synthesis.
Every lot of 2,6-Dinitrobenzonitrile leaving our reactors has to meet critical targets—appearance, assay, specific impurity profiles, and handling properties. Our typical specification ranges set purity at not less than 99 percent by HPLC, low moisture as determined by Karl Fischer titration, and individual impurity thresholds that demand highly refined reaction control. During early development, too many by-products complicated isolations and led to wasteful recrystallizations. By adjusting oxidation temperature ramps and tuning nitration agent ratios, we reduced choke points and managed crystal habit for easier downstream processing.
What that means for our clients is simple: a drum of our 2,6-Dinitrobenzonitrile doesn’t need extra labor to clean it up before use. Our plant’s experience has proved that attention to each filtration, wash, and drying stage pays off at the bench or in the pilot reactor outside company gates. Feedback from long-term partners—the sort who rarely get mentioned in glossy brochures—drives us faster than any generic specification sheet ever could.
We offer our standard 2,6-Dinitrobenzonitrile in several physical forms—fine, free-flowing powders or larger crystal fractions—because users often need to match handling with existing equipment. Filtering big batches through plate filters or feeding powders into continuous blenders can both run smooth, but each asks for a different style of product. Some of our partners have specialized pneumatic transfer rigs with very tight controls for airborne dust; for them, a slightly wetted cut improves safety and reduces static. Other clients prefer a lighter, lower-density powder that blends well, especially in custom solid formulations.
Physical model variation also helps when targeting process flow. At certain throughputs, a drier, denser powder fits right into automated charging systems designed for high-volume batch runs. Smaller labs might seek out a finer grind to dissolve quickly during routine scaling experiments. Guided by decades of hands-on advice, we’re constantly testing each batch for flow properties, compaction, and safe packing density—not just purity.
This compound plays a unique role in chemical synthesis. The nitro groups in the 2 and 6 positions—arranged on the benzene core opposite the nitrile—make it highly reactive under typical nucleophilic substitution conditions. Working with teams developing new pharmaceuticals or trying to scale up advanced pigment intermediates, we’ve seen how the electron-deficient nature of this molecule promotes coupling reactions that wouldn’t run efficiently with plain nitrile or a less activated ring.
Most users draw on 2,6-Dinitrobenzonitrile for two main purposes: as a key intermediate for active pharmaceutical ingredients, or as a building block in specialty dyes and high-performance resins. One notable example involves preparing complex aniline derivatives—especially for active drug scaffolds—where standard benzonitrile lacks the functionalization potential provided by the strong nitro groups. After repeated in-lab optimizations, process chemists found that using our compound cuts yields of unwanted by-products and shortens overall cycle time.
Some chemical building blocks tolerate a handful of trace contaminants; 2,6-Dinitrobenzonitrile does not. The presence of ortho- or para-isomers, incomplete nitration products, or residual oxidants can introduce headaches in downstream purification or, worse, poison palladium- or copper-based catalysts downstream. A few years ago, a partner in the fine chemicals sector flagged a recurring problem with catalyst fouling traced to a minor by-product below 0.1 percent. Our technical staff built an off-line purification loop and updated in-process controls in real time. This allowed us to guarantee consistently below-detectable impurity levels—even when production volumes increased—eliminating the root cause for all future batches.
Associating problem-solving with practical experience lets us jump ahead of many quality issues before they reach our loading docks. Hand in hand with our QC colleagues, we’ve invested in real-time impurity tracking and regularly calibrate detection limits to stay below published thresholds, not just on the final drum but in the reaction mixture and through each purification step. It takes more time and resources, but it’s saved a lot of customer downtime down the line.
A robust selection of commercial nitro-substituted benzonitriles exists, but the placement of nitro groups gives 2,6-Dinitrobenzonitrile its specific utility. Analogues such as 3,5-dinitrobenzonitrile or mixed mono-nitrobenzonitriles can function as mild activating groups, but seldom deliver the same regioselectivity in aromatic substitutions. Chemists aiming for selective nucleophilic aromatic substitutions find that the 2,6-dinitro structure lends superior reactivity without excessive side-product formation seen with more highly substituted rings.
In developing our process, we worked directly alongside users who exhaustively compared physical and chemical performance across a range of nitrobenzonitriles. Few alternatives matched the balance of activation and stability. The symmetrical substitution pattern of our molecule enables preparation of intermediates with few competing side-reactions, especially useful in large-scale reactions involving multiple steps and expensive reagents. Dyes and pigments using less activated analogues saw regrettable color shifts and lower yields after scale-up, illustrating the practical value of the 2,6-structure.
Decades working with aromatic nitriles and nitroaromatics taught us that effective safety and environmental controls are never optional. In the earlier years, we faced routine challenges in managing the nitro group’s reactivity during both synthesis and handling. Over time, upgrades in contained transfer systems, dust abatement, and well-trained staff have proven themselves with improved records and reduced near-misses.
Modern clients expect comprehensive assurances around handling risk, and so do we. Fresh batches are routinely analyzed for static hazards, sensitivity to impact, and vapor pressure. Our environmental team studies effluent streams for trace contamination and ensures any process improvements don’t shift problems from product to by-product. Whenever research suggests a better cleaning agent or a safer solvent, scale-up teams pilot these changes and roll out stepwise—one more lesson learned and built into the next operational plan.
Pharma developers and pigment formulators work at every conceivable scale, from milligrams to metric tons. Researchers tackling drug discovery run a reaction or two to test a synthetic route, then request kilogram quantities for scale-up. On the pigment side, routine recipes can move dozens of drums every month to feed global production lines. Our experience spans both extremes. Over the past decade, we’ve adapted to shorter cycle times and leaner buffer inventory systems demanded by just-in-time production partners.
Reliable supply of 2,6-Dinitrobenzonitrile supports these downstream goals. We respond to demand swings by maintaining real-time batch scheduling and a robust supply chain for precursor chemicals. If new specifications come in—say, a hard limit on sodium or chloride content for a critical synthesis—our process team pushes for an updated workup procedure and verifies compliance before shipping. Customers frequently ask for batch-specific impurity breakdowns, or request re-testing under their analytical conditions. Working from the manufacturing floor gives us the flexibility and real-world perspective to meet these changing needs, and to develop long-term trust.
Innovation at the plant level drives the progress behind every kilogram shipped. In some production runs, we’ve identified routes to recover heat or re-use cleaning solutions, cutting both cost and waste. Other improvements come from integrating better monitoring equipment—like inline HPLC—and from listening to our lab and operations staff about what’s slowing them down. Small tweaks in agitation speed, solvent addition protocols, or filter cake washing can yield measurable reductions in energy demand and turnaround time.
Our technical managers hold regular sessions with client process teams to review ongoing projects, collect feedback, and share our own production challenges. By exchanging candid stories about what works—or doesn’t—we help others avoid trial-and-error methods and get faster to scale. It’s not rare for a collaborative troubleshooting session to generate a new batch record, tooling recommendation, or updated safety note.
Interest in 2,6-Dinitrobenzonitrile rises alongside growth across pharmaceuticals, novel polymers, and specialty dyes. As downstream chemistry evolves—calling for tighter impurity limits, special packaging, or lighter carbon footprints—we have to anticipate needs several steps in advance. Regulatory requirements frequently shift, especially regarding solvent residues, allowable impurity levels, and environmental discharge. Our compliance staff works closely with manufacturing and R&D to adapt quickly. By aligning investment and training with emerging requirements, we keep both our partners and ourselves out in front of the next wave of demand.
Some users express growing interest in greener production methods or recycled solvents. We are piloting several new technologies—from solvent distillation upgrades to low-emission nitration agents—and sharing real-world experiences across the value chain. Where progress demands a shift in raw material sourcing or necessitates new waste stream treatments, the lessons are documented, and shared in joint project reviews with end users.
Managing cost while improving environmental and safety performance is an ever-present challenge. Higher purity and specialized physical grades require increased investment in plant and analysis, sometimes resulting in steeper production costs. These investments are balanced by the benefits—less rework, reduced downstream foulups, and tighter customer relationships anchored in reliability. Each feedback loop between our facility and your reactor leads to a smarter process for both sides.
No two production environments rely on the same configuration. Through years of work with clients across continents, we’ve fine-tuned our manufacturing to allow for custom packaging, documentation tailored to local regulations, and logistics planning suited for just-in-time delivery. Unplanned demand spikes and late-breaking changes in purity standards are part of the territory. We treat each as a chance to improve adaptability and reinforce trusted partnerships.
Collaboration extends beyond a sales contract. Whether it’s troubleshooting a stuck filtration in a plant, dialing-in a particle size for a batch of pigment, or re-validating a residual solvent level to satisfy a new compliance checklist, the relationship is built on pragmatic expertise. Our plant and technical staff talk daily with counterparts in R&D groups, pilot plants, and QA teams around the world. Sharing these real-world problems and solutions forms a connection much tighter than what commodity traders or catalogues could offer.
In side-by-side testing, users find that 2,6-Dinitrobenzonitrile achieves more efficient nucleophilic substitution than mono-nitro or differently substituted dinitrobenzonitriles. The symmetrical positioning of nitro groups on the aromatic ring drives higher yields and reproducibility. Research leads in pharmaceutical companies have commented on the improved selectivity during cyclization steps, which translates to less waste and cleaner intermediate isolations. Pigment manufacturers see consistent color development and fewer off-spec batches. These functional gains outweigh the upfront costs of securing higher-purity material.
Attempts to substitute simpler or less pure versions often create downstream bottlenecks. Our ongoing collaborations have turned up practical bugs in alternative materials: sludging in reactors, clogging in feed systems, or extended drying times for lower-grade raw materials. By diagnosing the true source of these bottlenecks—often minor impurities or the wrong particle size—our staff refines each batch to remove those obstacles before a shipment ever leaves our warehouse.
Having produced, handled, and shipped tons of 2,6-Dinitrobenzonitrile over the years, we’ve absorbed the tricks of the trade and carry forward improvements from every scale of manufacture. Real expertise emerges from troubleshooting, process adjustment, and never ignoring data from unexpected production days. Our lab managers, process engineers, and bulk handlers draw insight from every shipment that crosses our dock and every technical question coming in from the field.
We believe clear, candid communication matters most. If a process parameter, physical feature, or impurity cutoff matters for your application, we will tell you not just what is possible, but what might realistically improve outcomes in your own process. Across pharmaceuticals, dyes, and advanced engineering materials, users relying on tight process standards have seen their own product reliability rise when partnering with a manufacturer that knows every drum from the inside out.
This experience-driven approach sets us apart from the field, where generic technical sheets don’t capture the subtle factors that make 2,6-Dinitrobenzonitrile hit its mark every time. Whether you need help designing a better workflow, want to dig into a tricky reaction, or seek advice learning from years on the plant floor, our team stands ready to support your every batch.