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HS Code |
225101 |
| Chemical Name | 5-Chloro-3-nitro-2-pyridinecarbonitrile |
| Molecular Formula | C6H2ClN3O2 |
| Cas Number | 444731-29-9 |
| Appearance | Yellow solid |
| Melting Point | 91-95 °C |
| Solubility | Soluble in organic solvents like DMSO and DMF |
| Purity | Typically >98% |
| Storage Conditions | Store at 2-8°C, keep container tightly closed |
| Smiles | C1=CC(=C(N=C1C#N)[N+](=O)[O-])Cl |
| Inchi | InChI=1S/C6H2ClN3O2/c7-5-1-4(10(11)12)6(2-8)9-3-5/h1,3H |
As an accredited 5-Chloro-3-nitro-2-pyridinecarbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 5-Chloro-3-nitro-2-pyridinecarbonitrile, labeled with chemical name, hazard symbols, and batch information. |
| Container Loading (20′ FCL) | The 20′ FCL for 5-Chloro-3-nitro-2-pyridinecarbonitrile holds approximately 12-14 MT, packed in securely sealed fiber drums or bags. |
| Shipping | 5-Chloro-3-nitro-2-pyridinecarbonitrile is shipped in tightly sealed, chemical-resistant containers under ambient conditions. Proper labeling, documentation, and compliance with local and international hazardous material regulations are ensured. Shipping is typically via ground or air by authorized carriers, with safety measures to prevent leaks, contamination, and exposure during transit. |
| Storage | 5-Chloro-3-nitro-2-pyridinecarbonitrile should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect it from moisture, heat, and direct sunlight. Proper labeling and secondary containment are recommended to prevent leaks or spills. Only trained personnel should handle and access this chemical storage area. |
| Shelf Life | 5-Chloro-3-nitro-2-pyridinecarbonitrile is stable under recommended storage conditions; shelf life is typically 2-3 years in airtight containers. |
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Purity 98%: 5-Chloro-3-nitro-2-pyridinecarbonitrile with a purity of 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and minimal byproduct formation. Melting Point 130°C: 5-Chloro-3-nitro-2-pyridinecarbonitrile with a melting point of 130°C is used in agrochemical formulation, where it allows for stable processing and precise blending. Particle Size <10 µm: 5-Chloro-3-nitro-2-pyridinecarbonitrile with a particle size less than 10 micrometers is used in fine chemical production, where it improves suspension uniformity and reaction efficiency. Moisture Content <0.5%: 5-Chloro-3-nitro-2-pyridinecarbonitrile with a moisture content below 0.5% is used in catalyst manufacturing, where low moisture prevents hydrolysis and maintains catalyst activity. Stability Temperature up to 200°C: 5-Chloro-3-nitro-2-pyridinecarbonitrile with stability up to 200°C is used in high-temperature organic synthesis, where it preserves structural integrity and reaction consistency. |
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Every day in the plant, the crew and I work with a lot of heterocyclic compounds, but 5-Chloro-3-nitro-2-pyridinecarbonitrile, sometimes known among labs as 5C3N2PCN, truly stands out in its chemical family. Our path toward perfecting its synthesis didn’t begin with a vague interest; it started from repeated calls by process chemists, agrochemical developers, and API researchers for a nitrile-substituted pyridine that stays reliable batch after batch. They wanted sharp consistency, not just standard purity.
This compound isn’t simple or forgiving during production. Its model structure—a chloro and nitro on the same pyridine ring with a cyano group anchoring the 2-position—creates some real challenges at scale. Early trials, we ran into runaway exotherms, sudden darkening, and filter cakes that refused to dry. Our team solved these hurdles, not by following recipes, but by tuning each step to give stable, nearly off-white to pale yellow solid with a typical melting point range nested around 142 to 146 °C.
The most productive feedback came from pilot batches sent to a research hospital’s medicinal lab. They reported clean TLC profiles, high conversion rates in substitution reactions, and, more importantly, no signs of chloro group displacement under standard reduction. This insight helped us tweak our work-up process, reducing clamp time by nearly three hours per batch and cutting residual solvent to minimal levels.
We’ve made a point to keep this product’s specifications tight because even a half percent more moisture or unwanted residual anion can throw off the results for a process chemist. Each lot comes off our reactor line with a minimum purity of 99% as determined by HPLC. Water content isn’t just an afterthought. We keep it below 0.3%, checked by Karl Fischer. Typical GC-MS scans show little to no major byproducts. For a product as sensitive as this, we’re strict with packaging and storage, using only high-density polyethylene drums with silica packs, especially for international shipments.
Our average lot size ranges from 20 kg to 300 kg, although small-volume labs often request a few grams for screening. Many buyers ask about appearance, and from our own inspection, the solid settles into a fine, easily dispersible powder. It’s not prone to caking unless left exposed for hours in humidity common in coastal factory towns. We haven’t seen hazardous dusting under controlled handling, though our team always works under local exhaust ventilation, as the nitro group brings some expected toxicology concerns.
We’ve seen firsthand that 5-Chloro-3-nitro-2-pyridinecarbonitrile has carved itself an important niche in the intermediate field, especially among agrochemical syntheses and certain pharmaceutical R&D projects. Customers pursuing programs in pyrazole and triazine research favor this building block for its reactivity profile. The electron-withdrawing nitro and cyano groups open up tailored substitution on the pyridine ring, and the chloro site resists unwanted exchange when handled under standard nucleophilic aromatic substitution conditions.
Some factories use it as a precursor for crop protection agent synthesis. We heard from one of our earliest partners—a mid-sized agro formulator—that our product sharply increased their yield in the step linking the pyridine subunit to an amide backbone. For pharma, the appeal centers on how reliably our process suppresses the 3,5-dinitro impurity. Medicinal chemists at a contract research site told us they landed solid SAR data only after switching to our lots, avoiding headaches from trace isomers that plagued earlier studies.
In our experience, chemists often compare 5-Chloro-3-nitro-2-pyridinecarbonitrile to relatives like 2,3-dichloropyridine or 3-nitro-2-chloropyridine. These may share certain ring activation patterns, but the presence of both nitro and nitrile at the 3 and 2 positions opens up reaction scope our clients never achieved with the others. The combination changes not only reactivity in Suzuki or Buchwald couplings but also influences regioselectivity in metal-catalyzed C-H activation. We’ve run several in-house case studies tracking reaction outcomes, and each time, 5-Chloro-3-nitro-2-pyridinecarbonitrile delivered cleaner conversions with fewer side products.
Another distinct difference: the risk profile. Colleagues new to this compound sometimes expect simple hazards, but you need a team trained for energetic nitroaromatics and cyanides. Our entire process line uses double-contained transfer and active fume removal systems. Compliance and safety aren’t buzzwords in our plant—they grow out of real-world accidents and corrections.
On the factory floor, longtime operators often remind new hands: never cut corners on containment when weighing this material. It doesn’t fume at room temp, but grinding or transfer can send fine particles airborne. Full nitrile gloves, sleeves, and splash goggles are standard. Anyone nearby knows the sharp, faintly acrid smell, and even trace contact causes skin dryness or irritation for sensitive folks. Our usual practice calls for running all blending and aliquoting inside gloveboxes or negative pressure workstations.
Waste management plays a leading role at our site. We neutralize any mother liquors by sequential dilution and treatment with mild reducing agents, not only to keep compliant with environmental regulations but to avoid surprise reactions in the drum yard. Plant supervisors check pH and nitrite content before offloading. Once the batch clears QC, the residue and filter cakes get sent in closed, barcoded containers for licensed incineration.
As a direct manufacturer, we never rest easy after shipment. We expect to hear back from synthetic chemists on every lot, not just on quality but on how a new batch runs in their hands. Over the years, our customers have helped us spot minor issues—from an unnoticed shift in crystal morphology caused by a mid-year humidity snap, to rare gelation in the mother liquor. Each time, we review reactor logs and sample retainers to find the variable and push improvement into the next sequence. These lessons rarely make a glossy spec sheet, but they drive every change in our process.
In our meetings with contract drug manufacturers, some teams report gel plug formation during downstream purification. Our technical group traced this back to a shift in one filtration protocol and changed both mesh size and drying parameters to stop the clumping altogether. With every trial and blunder, our shop floor learns how far careful adjustments can go in improving real-world workflows—not just lab data.
If you’ve ever waited for an urgent delivery, you know the real value of supply isn’t in a bullet proof spec or a pretty report; it’s in honest, timely batches that match the last shipment. Our crews label and sample every drum with dual records—digital and physical—so callbacks or investigations never hit a dead end. If a customer needs to audit a batch, records go back five years, from raw material test reports to operator shift notes and final product ref ID. We visit each storage site at least twice a year to test samples for degradation, especially for lots stored over six months. You learn fast in chemical manufacturing that customer trust doesn’t come from claims but from repeat evidence in the bottle, batch after batch.
Manufacturing a compound like this confronts us with heavy choices about environmental impact. Early on, our old vent scrubbers struggled to remove chloro and nitro traces. The emissions reading set off alarm bells, not just with regulators but within our local community. So our plant invested in more advanced two-stage acid scrubbers and digital stack monitoring—changes spurred by mistakes made and neighbors who demanded honest dialogue. Every year, we analyze waste streams for residual cyanide and nitro byproducts using in-house LC-MS, adjusting procedures with every noticeable spike.
We also switched from single-use drums to reconditioned ones where possible, pushing our partners to accept regular cycle retrieval for cleaning and reuse. Nothing about these improvements came easy; every step needed retraining crews, updating SOPs, and working out bumps with auditors and fire marshals. But a cleaner operation translates into easier product compliance and often more reliable shipments, since regulatory freezes and plant shutdowns have dropped to near zero since these updates. In other words, putting in the work pays off for us and our customers.
Many customers buying 5-Chloro-3-nitro-2-pyridinecarbonitrile for the first time underestimate both its advantages and the complexity of handling it. Some plan on direct scale-up from small flask experiments, only to find that reaction rates, impurity formation, and even filtration behaviour changes completely above 500 grams. Others run into unexpected thermal decompositions if they skip inert atmosphere transfer during high-temp steps. In our technical discussions, we emphasize practical points: monitor exotherms, keep tight control on solvent grade, and have an exit plan for any side-generated cyanides.
Our support team fields questions every week about synthetic routes—what works, what fails, and what no spec sheet reveals. Most often, trouble comes from trying to shortcut reaction order or skipping a wash. We keep a full log of alternative coupling partners and quenching agents that our customers have tested successfully, and we exchange these real-world results freely with serious buyers.
We don’t see ourselves as a generic source or off-the-shelf label. We manufacture each lot of 5-Chloro-3-nitro-2-pyridinecarbonitrile from raw stock to finished, QC-passed product under our own roof. This makes traceability, consistency, and flexibility easier to manage than outsourcing or drop-shipping ever could. Our team regularly re-examines each process step, from early nitration to final drying, because even a slight drift in one reactor run translates into wasted hours for our customers. This feedback cycle between factory hands, QC lab, and end users gives us an edge you can’t find in generic distribution.
Raw materials come only from approved, audited partners with full COA and internal screening. Before each production sequence, we pre-test all solvents and precursors for halide and nitrate contamination, because running a batch with compromised input means higher side product and lost yield. We developed our own in-line monitoring for reaction progress to spot off-spec conditions in real time. It’s painstaking work, but it pays dividends downstream—yield, purity, worker safety, and customer reassurance.
A lot goes into making this product right—the smell of the piles of wet filter cake, the quiet tension during the first hours of each nitration run, and the satisfaction when each kilogram leaves the QC lab with a clean report. Every operator, analyst, and line supervisor knows the stakes, because we’ve seen the surprise errors than can creep up in a rush batch, or the ripple effects from an unchecked impurity. We run frequent shift meetings to review any process deviation, regardless of how small. A transparent, feedback-driven culture—as dull as it may sound outside the plant—does more for reliability and trust than any poster on the breakroom wall.
We plan ongoing upgrades in our production line by leveraging data from each shipment and feedback cycle. New in-situ sensors for temperature and pH cut our reaction time by nearly five percent, and we’ve started using digital logs for real-time tracking of every drum filled. Exploring greener reaction conditions is a current focus; our R&D lead has been testing replacement oxidants with lower aquatic toxicity, and early results suggest a measurable drop in EHS risk per batch. If these trials pan out, customers will see even lower impurity drift and a smoother regulatory path with certain end uses.
We hold regular technical exchanges with other direct manufacturers and industry groups, comparing results openly. Every insight, every minor process shift, carries through our operation—never sitting idle on paper or left as an afterthought.
From dozens of pilot projects, scaled-up manufacturing campaigns, and long nights next to the reactor, we’ve come to trust what this compound can do when produced with care. Seasoned customers value not just the label appearance, but repeatable quality and deep traceability, year after year. Spec sheets and batch records only tell part of the story; real assurance grows out of hard-won experience and a willingness to adapt every time the chemistry demands it.
If you need an intermediate where every impurity counts, where reproducibility writes the bottom line of your process, and where supplier know-how matters just as much as raw purity, this product remains a smart, proven choice—shaped by every hands-on lesson learned in our own manufacturing plant.