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HS Code |
720838 |
| Chemical Name | 2-Pyridinecarbonitrile, 5-chloro-3-nitro- |
| Synonyms | 5-Chloro-3-nitropicolinonitrile |
| Molecular Formula | C6H2ClN3O2 |
| Molecular Weight | 183.56 g/mol |
| Cas Number | 87333-70-6 |
| Appearance | Yellow solid |
| Melting Point | 113-115°C |
| Solubility | Slightly soluble in common organic solvents |
| Structure Smiles | C1=CC(=NC(=C1Cl)[N+](=O)[O-])C#N |
| Logp | 2.0 (estimated) |
| Density | 1.6 g/cm³ (estimated) |
As an accredited 2-pyridinecarbonitrile, 5-chloro-3-nitro- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with tamper-evident cap, chemical label displaying hazard symbols, product name "5-Chloro-3-nitro-2-pyridinecarbonitrile." |
| Container Loading (20′ FCL) | Container loading (20′ FCL): Loaded in 25 kg fiber drums, 8 MT net weight per 20-foot container, on pallets, secured for transport. |
| Shipping | 2-Pyridinecarbonitrile, 5-chloro-3-nitro- is shipped in tightly sealed, chemically resistant containers under dry conditions. Transport complies with relevant hazardous material regulations, including appropriate labeling and documentation. The substance should be kept away from heat, moisture, and incompatible materials throughout shipping to ensure safety and chemical stability. |
| Storage | 2-Pyridinecarbonitrile, 5-chloro-3-nitro- should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and reducing agents. Protect from light and moisture. Store at room temperature and avoid sources of ignition. Ensure proper labeling and restrict access to trained personnel only. Use secondary containment if available. |
| Shelf Life | 2-Pyridinecarbonitrile, 5-chloro-3-nitro- typically has a shelf life of 2-3 years when stored tightly sealed, cool, and dry. |
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Purity 98%: 2-pyridinecarbonitrile, 5-chloro-3-nitro- with purity 98% is used in pharmaceutical synthesis, where it ensures high reaction yield and minimal impurities. Molecular weight 183.56 g/mol: 2-pyridinecarbonitrile, 5-chloro-3-nitro- of molecular weight 183.56 g/mol is used in agrochemical intermediate production, where it facilitates targeted compound formulation. Melting point 123°C: 2-pyridinecarbonitrile, 5-chloro-3-nitro- with a melting point of 123°C is used in organic synthesis, where it allows for controlled thermal processes. Particle size ≤20 µm: 2-pyridinecarbonitrile, 5-chloro-3-nitro- at particle size ≤20 µm is used in fine chemical manufacturing, where it enhances dispersion and reactivity. Stability temperature up to 80°C: 2-pyridinecarbonitrile, 5-chloro-3-nitro- stable up to 80°C is used in catalyst research, where it maintains structural integrity during elevated temperature reactions. Solubility in DMF: 2-pyridinecarbonitrile, 5-chloro-3-nitro- soluble in DMF is used in advanced material synthesis, where it achieves homogeneous mixing and efficient processing. |
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Anyone involved in pesticide synthesis or pharmaceutical intermediates knows how often the small details make or break a process. From our years handling dozens of substituted pyridine compounds, it’s plain that 2-pyridinecarbonitrile, 5-chloro-3-nitro pulls its weight when selectivity, reactivity, and stability really matter. We run several lines of substituted nitriles, but this variant has a reputation for reliability in both research and production environments. Chemists ask for it by name because it answers the call for a balance of electron-withdrawing power from the nitro group and the activating character of the chloro substituent at the right spots on the ring.
In our own labs and at customer facilities, this material sees repeated use in synthesis of heterocyclic building blocks. Its structure supports both nucleophilic and electrophilic substitutions, which opens doors for crafting complex molecules without slogging through exhaustive protection and deprotection steps. The experience on the ground is that this compound—with its chloro and nitro pattern—offers cleaner downstream product profiles and minimizes unpredictable byproduct formation compared to some other pyridinecarbonitriles.
Through years of process refinement, we’ve learned a thing or two about producing high-quality 2-pyridinecarbonitrile, 5-chloro-3-nitro on scale. The nitro and chloro substitution, specifically at the 3 and 5 positions, not only tune the molecule’s electronic effects for end-use applications but also matter during isolation, crystallization, and drying in the plant.
In our facility, we adopted a gradual solvent switch-out technique during crystallization, which cuts down on clumping and improves filtration rates. Repeated field feedback guided every change: users wanted cleaner product with higher shelf stability and fewer issues on dissolution when charging their reactors. Once handled or stored, this compound proves robust: it resists decomposition and maintains its appearance far longer than less stable nitriles.
Batch records support this. One of our lots sent overseas last year maintained full assay and clarity nearly 18 months post-shipment. The feedback from regular users—especially those in fine chemicals and custom synthesis—echoes this experience. Formulators mention less downtime and fewer headaches reworking dissolutions or scrubbing glassware, which means more productive shifts and real savings.
Chemists in our network have leveraged this compound primarily as an intermediate for agrochemical actives like fungicides and herbicides. The robustness of the nitrile lets it survive harsh conditions, while the chloro and nitro groups guide the transformation down the target pathway, often feeding directly into Suzuki, Buchwald, or nucleophilic aromatic substitution steps.
Our own pilot projects targeted heterocyclic building blocks—several of which now underpin newer generation APIs. The efficacy isn’t just in literature claims: from each kilo shipped, teams are realizing higher yields, using fewer purification steps, and meeting specifications for impurity profiles when they introduce this material compared to alternatives. More than one customer reported that switching to this compound, even at moderate scale, trimmed costs by cutting out labor and solvent use linked to repetitive purifications.
We routinely get asked: how does this compound compare to 2-pyridinecarbonitrile without substituted groups, or ones with only a nitro group? The electronic effects from both the chloro and nitro substituents—properly spaced—effectively tune the molecule’s reactivity. The parent pyridinecarbonitrile proves more susceptible to side reactions, especially under strong basic or reducing environments. Single nitro analogues work in milder conditions, but they don’t always deliver clean conversions for more ambitious substitutions.
The combined substitution in this 5-chloro-3-nitro version blocks unwanted reactions on the ring, decreasing competitive side products. This shows up in actual process data, not just theory. As an example, one batch of downstream sulfonamide synthesized from this intermediate yielded 10% higher product, all while reducing off-spec byproducts during our campaign. That’s not a fluke—colleagues at two custom synthesis houses later reported similar performance in their own continuous flow setups.
There’s another difference that process engineers notice. The solubility window for this compound fits industry-standard solvents better than other variants. Running a solvent screen in our kilo lab, we found that common polar aprotic solvents dissolve this product consistently, supporting smooth charging and reliable precipitation in high-throughput operations.
Running production at scale, we see a range of challenges nobody mentions in textbooks. Fine particle size from suboptimal crystallization fouls up downstream filtration and creates airborne dust—not just a mess, but a real safety concern. Through recent upgrades, we narrowed down process parameters and now consistently produce material in a flowable, low-dust form, thanks to tweaks in cooling rates and feed composition.
The outcome isn’t academic. Shelf stability improves. Handling losses in the plant drop, which matters for every operator transferring drums or filling bins. Someone working with sticky, agglomerated intermediates knows how stressful repeated downtime can become; with this compound’s improved free-flow properties, those worries drop away. There’s less compensation for absorption losses, and the material dispenses precisely for both kilo- and multi-tonne campaigns.
No matter the downstream use, purity specifications and in-process analysis drive everything. Customers rarely compromise on specs. Our experience reminded us years ago to exceed minimum requirements—the more critical the intermediate, the higher the stakes if off-target impurities show up.
Analytical QC methods—HPLC, NMR, and melting-point checks—have been standardized at our facility, using certified reference standards. Through repeated validations, we tightened our spec to typical minimum assay of 99% by HPLC, routinely delivering above that mark. Impurity control runs below 0.2% for individual knowns, with no single unknown above 0.05%. Running shorter cycle times and pilot-scale demos always confirmed our QC lines: no failed lots in two fiscal years despite rising output.
The biggest benefit rests with end-users. Predictable purity enables tighter process optimization. In practice, chemists realized more repeatable process runs when switching to our material, reflected in higher batch acceptance rates. That, in turn, slashed reject waste and batch-to-batch variability, which matters to anyone balancing their own cost sheet and output targets.
Substituted pyridinic nitriles can cause headaches outside the reaction flask, clogging feeders, gumming up augers, or reacting with drum linings after months in storage. We prepare our batches using moisture-controlled blending and drum lining materials proven to minimize static and caking. Plant workers now unload material more easily, whether charging a 500-liter reactor or weighing a small-scale synthesis run for medicinal chemistry.
Customers report fewer disruptions from caked product, good flow rates during transfer, and—most importantly—minimal odor or air release on handling. Since many fine chemical processes fail when intermediates degrade during storage, a well-behaved material pays dividends in both safety and efficiency. In-house testing records back up these observations, with compounding staff noting no detectable yellowing, caking, or loss of reactivity, even after six months of warehouse storage.
People working daily with these compounds care about both personal safety and environmental impact. Early process trials told us which solvent choices lower environmental risk, and we adopted closed-loop solvent recovery to keep emissions and waste below regulatory triggers. Our waste treatment unit deals with mother liquors and residues in line with local and international protocols, based on direct collaboration with EHS consultants and compliance officers.
Inside the plant, careful monitoring with hand-held VOC sensors led to ventilation upgrades at drum filling points. This means consistently lower workplace exposures—actual measured air levels rest below published threshold values. The result is lower personal exposure risk, but also less unscheduled downtime for area purging or filter replacement. Workers appreciate these improvements, and operators now handle the material without the recurrent complaints that plagued earlier setups.
Disposal of wastes connected to 2-pyridinecarbonitrile, 5-chloro-3-nitro does need close attention—our plant follows the most current hazardous waste tracking guidance, coupled with batch labeling for transparent documentation. Longer term, these improvements put us in a more sustainable position: less solvent, lower energy use per ton, and more manageable waste volumes.
Anyone who has switched suppliers or intermediates mid-project understands the risk to supply continuity. Several partners moved over to our line of substituted pyridinecarbonitriles after experiencing delayed shipments or quality variation from other channels. Since we manufacture on dedicated equipment (no campaign sharing with unrelated products), cross-contamination risks don’t arise.
Production scheduling and raw material management keep our lead times short, cutting typical delays for synthesized batches. We maintain buffer stocks of key inputs—halogenating agents, nitro substitutions, and high-purity solvents—all stored onsite to cover scheduled and emergent production runs. On rare occasions when raw material disruptions threatened output, pre-arranged supply agreements bridged the gap, ensuring continuous fulfillment for long-term buyers.
Direct relationships with logistic providers, as well as proper packing under nitrogen where required, have prevented issues like transit degradation or loss of assay. Each drum, carton, or package leaving our site includes full batch records and shipment certifications—not as marketing fluff, but as tangible deliverables our partners audit before production kicks off at their own plants.
Interest in substituted pyridine intermediates only grows as pharmaceuticals and crop protection chemistry grow more sophisticated. End-users—ranging from campus research groups to global agrochemical companies—demand intermediate molecules that enable their scientists to experiment, scale, and innovate without recurring delays. In survey feedback and technical visits, lead chemists stressed their need for predictable, high-purity supply chains. Prompt, reliable shipments of 2-pyridinecarbonitrile, 5-chloro-3-nitro have repeatedly meant they hit commercial launch or pilot targets.
A few specific stories reinforce these observations. In the past twelve months, a pharma startup took delivery of material for a newly developed kinase inhibitor project. Their chemists noted reproducible yields batch to batch, with no rework for failed HPLC runs. For one formulation campaign, a crop protection firm commented that impurity drift dropped once they integrated our product. Quantifiable benefits like these set useful benchmarks.
Several clients also pointed out the stability and reliable flow properties matter as their own teams migrate from batch to flow chemistry. Feedback from these application shifts informs our fine-tuning—from tweaking particle size distribution, to reviewing every aspect of our product packaging.
Manufacturing this compound built a body of internal expertise around not just the synthetic route, but the tiny adjustments that transform lab curiosity into genuine plant reliability. Chemistries that look straightforward in the literature require relentless attention to detail in a real-world facility—right down to how cooling rates shape crystal habit, or how minor pH tweaks during workup slash downstream rework.
Through thousands of production hours, cross-checks, and real-life customer experiences, we keep raising our benchmarks for purity, consistency, yield, environmental footprint, and usability. Our investment in dedicated lines, process safety, and upstream control means that scientists relying on our 2-pyridinecarbonitrile, 5-chloro-3-nitro can meet project targets with fewer headaches and more productivity. Whether synthesizing fine chemicals, scaling new molecules, or de-risking a global rollout, partners recognize the value that comes from working directly with a manufacturer who understands both the science and the field realities this compound touches every day.