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HS Code |
492121 |
| Chemical Name | 5-chloropyridine-3-carbonitrile |
| Molecular Formula | C6H3ClN2 |
| Molecular Weight | 138.56 g/mol |
| Cas Number | 89846-37-3 |
| Appearance | light yellow to brown solid |
| Melting Point | 61-65°C |
| Boiling Point | 278-280°C |
| Density | 1.32 g/cm3 (estimated) |
| Solubility | sparingly soluble in water, soluble in organic solvents |
| Smiles | C1=CC(=CN=C1C#N)Cl |
| Inchi | InChI=1S/C6H3ClN2/c7-5-1-6(3-8)9-2-4-5/h1-2,4H |
| Synonyms | 5-Chloro-3-cyanopyridine |
As an accredited 5-chloropyridine-3-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "5-Chloropyridine-3-carbonitrile, 98%, 25g." Features hazard pictograms and tightly sealed screw cap for safety. |
| Container Loading (20′ FCL) | 20′ FCL loading for 5-chloropyridine-3-carbonitrile ensures secure, efficient bulk packaging, minimizing contamination and optimizing space for international shipment. |
| Shipping | 5-Chloropyridine-3-carbonitrile is shipped in tightly sealed containers, compliant with chemical safety regulations. It should be stored in a cool, dry, and well-ventilated area, away from incompatible substances. Proper labeling and documentation are required. Shipping follows relevant regulations for hazardous materials to ensure safe handling during transit. |
| Storage | 5-Chloropyridine-3-carbonitrile should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Keep the container tightly closed and clearly labeled. Store at room temperature, protected from moisture and direct sunlight. Ensure appropriate spill containment and use personal protective equipment when handling this chemical. |
| Shelf Life | 5-Chloropyridine-3-carbonitrile should be stored tightly sealed, in a cool, dry place; shelf life is typically several years if unopened. |
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Purity 99%: 5-chloropyridine-3-carbonitrile with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimized impurities in active pharmaceutical ingredients. Melting Point 103°C: 5-chloropyridine-3-carbonitrile with a melting point of 103°C is used in agrochemical manufacturing, where it provides controlled reactivity and stable processing conditions. Molecular Weight 138.55 g/mol: 5-chloropyridine-3-carbonitrile with a molecular weight of 138.55 g/mol is used in heterocyclic compound synthesis, where precise stoichiometry enhances reaction efficiency. Particle Size <75 µm: 5-chloropyridine-3-carbonitrile with a particle size less than 75 µm is used in solid formulation blending, where it enables homogeneous mixing and improved formulation consistency. Stability Temperature up to 120°C: 5-chloropyridine-3-carbonitrile with stability up to 120°C is used in high-temperature catalytic reactions, where it maintains structural integrity and reaction selectivity. Water Content <0.1%: 5-chloropyridine-3-carbonitrile with water content below 0.1% is used in moisture-sensitive organic syntheses, where it prevents unwanted hydrolysis and side reactions. HPLC Assay 99.5%: 5-chloropyridine-3-carbonitrile with an HPLC assay of 99.5% is used in active ingredient preparation, where it contributes to reproducible bioactivity and product consistency. Residual Solvent <500 ppm: 5-chloropyridine-3-carbonitrile with residual solvent below 500 ppm is used in fine chemical production, where it meets stringent regulatory requirements for purity and safety. |
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People in chemical research and industry sometimes glaze over at the long names and cryptic numbers attached to intermediates, but behind each formula is a real engine of change. Take 5-chloropyridine-3-carbonitrile. It's not some obscure molecule gathering dust on a lab shelf. This compound, a chlorinated pyridine with a cyano group at the third position, brings together two reactive sites that open up a strong path for finer modifications and downstream synthesis.
What drew me to this intermediate is its straightforward structure combined with room for creative manipulation. Once I hit the bench with it, the convenience of the molecule became clear. Chlorine at the five-position and that electronic-pulling cyano group combine to create not just a flexible building block, but an efficient tool for constructing active ingredients and performance materials.
Not every intermediate delivers on both reactivity and stability. Many compounds with activated halogens will hydrolyze, brown, or degrade before you even set up your reaction, especially under water-sensitive or multi-step conditions. With 5-chloropyridine-3-carbonitrile, there’s real confidence in the bottle—this substance keeps well, stands up through repeated handling, and allows for predictable outcomes at each stage.
Where I’ve seen its strength is in forming coupling products, especially when you need a clean aromatic starting point. While some alternatives containing multiple halide groups tend to be too reactive or cross-link by mistake, the mono-chloro variant hits a sweet spot. Handling is less hazardous, yields become more reliable, and the work-up is a little less of a headache.
Most conversations about 5-chloropyridine-3-carbonitrile start in a pharmaceutical context. The molecule we’re talking about finds its way into the construction of kinase inhibitors, fungicides, and other advanced molecules. A key example comes from synthesizing pyridyl-based active pharmaceutical ingredients, which often demand a chlorinated building block to anchor further transformations. When large companies in drug discovery trace the origin of their heterocyclic scaffolds, this intermediate shows up more often than most folks would guess.
Agricultural chemistry also relies on these compounds, particularly for next-generation crop protection agents. Whether you’re aiming for an insecticide or a herbicidal backbone, the reactivity profile lets you build new carbon-nitrogen bonds or introduce further functionality, depending on the demand. This flexibility speaks directly to the changing needs of modern agrochemical development, where agility matters as much as potency.
Specifications get tossed around a lot, but the ones that shape experience in the lab are purity, melting point, and particle size. When working with 5-chloropyridine-3-carbonitrile, a typical expectation might involve a purity exceeding 98 percent, given strong chromatographic clarity and little to no visible by-products. The melting point generally falls within a tight range, which reduces surprises during purification and downstream coupling reactions. Consistency matters when you move from milligrams to kilos—a lesson I learned the hard way during scale-up runs where every impurity could turn into an unknown side product.
Particle size matters when handling is frequent. Powder flow, static build-up, and clumping are common gripes, but a well-prepared batch of this intermediate stays manageable. Whether weighing into a round-bottom flask or feeding into a flow reactor, these practical handling properties cut down on batch-to-batch headaches and let researchers focus on what matters most.
Laboratory synthesis is only the beginning. As someone who’s worked in both the fine chemicals and pharma spaces, I’ve seen 5-chloropyridine-3-carbonitrile serve as a launchpad for a wide spread of routes. Structural modifications often start with selective substitution at the chloro position. A typical use-case involves nucleophilic aromatic substitution (SNAr) to introduce amino, alkoxy, or thiol groups. Each route spawns a library of analogs for biological testing or materials development.
Medicinal chemists often look for intermediates that support fast structure-activity relationship (SAR) campaigns, where versatility means everything. Cyano groups at the third position offer a handle for further functionalization, including reduction to amines or further elongation to acids. Looking back at my lab notes, the number of routes that become accessible with this combination of functions exceeded expectations, especially when integrating with palladium or copper-catalyzed cross-couplings.
The reach of this intermediate isn’t limited to pharmaceuticals or agrochemicals. Specialty polymer manufacturers have picked up this building block to introduce nitrogen-rich sites into high-performance polymers. Flame retardants and specialty pigments, often invisible to the end user, benefit from its presence in their synthetic route. The chemistry that starts here spreads out into coatings, dyes, and specialty adhesives—applications often overlooked, yet fundamental to boosting product quality downstream.
The bench is crowded with pyridine derivatives—chloro-, bromo-, iodo-, and more—but the choice isn’t about what’s just available. It’s about what works predictably and safely. Many practitioners default to 2- or 4-chloropyridines because of historic precedent. Yet, moving the halogen and cyano functionalities to the 5 and 3 positions, respectively, opens up the molecule for differentiated reactivity. For example, 2-chloropyridine derivatives often display steric hindrance, which can bottleneck reaction rates and limit yields for bulkier nucleophiles. Bromo and iodo analogs, while more reactive, come with higher cost and increased environmental concerns, plus handling risks not every lab wants to take on.
From a sustainability angle, chlorinated compounds sometimes carry baggage, and rightly so. Synthetic strategies and waste-handling protocols have evolved, and the current processes available for this intermediate show real progress. When I have had to justify a synthesis route on account of by-product minimization and recyclability, 5-chloropyridine-3-carbonitrile has provided a compromise between performance and process load. Unlike some earlier-generation reagents, the molecule can often be incorporated into greener workflows with less caustic waste streams.
With any halogenated intermediate, safety demands respect. The process safety profile matters just as much as the theoretical yield. Exposure to chlorinated aromatics calls for careful ventilation, monitoring of reaction off-gassing, and proper PPE. Through experience, I’ve seen teams maintain smooth operations simply by elevating these procedures from “best practice” to standard operating procedure—pairing knowledge with meaningful action.
The cyano group sometimes prompts concern due to its potential to release hydrogen cyanide under harsh conditions. In most synthetic routes I’ve encountered, this risk remains low when reactions stick to standard protocols. Chemistry demands vigilance, not fear-mongering. By applying robust engineering controls and sound judgment, even higher-volume facilities manage these risks effectively. In my time in scale-up suites, consistent risk assessment quelled surprises and fostered a safer working environment.
My own appreciation for 5-chloropyridine-3-carbonitrile grew as the molecule loosened bottlenecks on real projects. Time and again, projects stall at the intermediate-building stage, waiting on a complex scaffold or a reactant with unreliable sourcing. Colleagues in procurement and project management echo this, noting how compounds with clear production pathways and multiple suppliers reduce project delays and cost overruns.
One example comes from a lead optimization campaign that nearly unraveled over a missing batch of a competitor’s 2-chloropyridine analog. In contrast, the procurement of 5-chloropyridine-3-carbonitrile, sourced from more stable production pipelines, kept the project on schedule. This isn’t just about saving face or hitting deadlines; it’s about maintaining morale across the lab, business, and regulatory teams.
Working with a reliable intermediate lets people spend energy on creative chemistry, not firefighting logistical problems. Success in synthesis and process improvement strengthens team belief—something that spreadsheets and databases often miss but which shows up in better products and faster progress.
Supply chain resilience has become a hot topic. Not so many years ago, it wasn’t uncommon to see researchers halted by interrupted shipments or poor batch consistency. Changes in global logistics reveal weaknesses fast, and companies focusing only on short-term pricing find themselves burned by missed milestones and lost opportunities.
From my experience, 5-chloropyridine-3-carbonitrile entered the scene as a model for what reliable intermediates should look like. Suppliers offering consistent quality, prompt documentation, and secure logistics built real trust among procurement managers and chemists alike. An uninterrupted flow of the compound keeps pilot plants running, lets kilo-labs focus on scaling up, and avoids the last-minute panic that comes with a botched delivery or a poorly documented certificate of analysis.
Bringing transparency to specifications and performance builds knowledge and assurance for everyone involved. This approach makes the product appealing not only for chemists who need results today but also for technical managers planning tomorrow’s launches. In a world where custom manufacturing and contract research organizations play a bigger role, flexibility and reliability matter more than ever.
Stepping away from purity percentages and melting points, what matters most is performance under pressure. In pilot programs and finished product launches, reproducibility drives both innovation and regulatory acceptance. Whether building a new pesticide or scaling up an orphan-drug candidate, the knock-on value of reliable intermediates can’t be overstated.
Coming up against regulatory deadlines or unexpected changes in product formulation, teams leveraging 5-chloropyridine-3-carbonitrile stand a better chance at threading the needle—meeting both internal goals and external compliance. The molecule’s wide acceptance and regulatory track record accelerate approvals for downstream compounds, trimming red tape while upholding safety and quality.
As seasoned formulators know all too well, a problematic intermediate saps resources, damages project scores, and eats away at team momentum. With this compound, projects move in a straight line from concept to scale, with fewer acrimonious meetings and more room to focus on solving new challenges.
The path from starting materials to final product isn’t always smooth. Process chemists who view intermediates as fixed points on a flowchart miss real chances for creativity. Through trial, I’ve found that small changes in feed order, reaction conditions, or purification techniques with 5-chloropyridine-3-carbonitrile lead to disproportionate benefits—boosting yield, reducing impurities, or cutting cycle time.
Whether through experimentation with solvents or integration with continuous flow reactors, the intermediate's stable nature means you don’t have to chase decomposed by-products or spend hours troubleshooting columns. That reliability frees up time for actual process optimization, which moves the field ahead in practice, not just theory.
For those pursuing green chemistry, the molecule’s manageable risk and straightforward purification lower the environmental impact compared to some bulkier or multi-halogenated options. Working with operations and EHS teams, integrating process improvements dovetails with sustainability goals, benefitting business, team safety, and the environment.
Quality assurance sometimes feels disconnected from the day-to-day dance of synthesis and scale-up. Still, long-term success often depends more on the nuts-and-bolts work that happens before anyone sees a final product. Each time I’ve worked on a validation or quality audit involving 5-chloropyridine-3-carbonitrile, the robust documentation and traceable supply chain history made a real difference.
Good suppliers back up each shipment with full analytical support and regular validation of consistency. That means fewer deviations, less rework, and greater confidence for anyone using the molecule downstream. Whether qualifying a batch for a new product launch or passing a tough third-party audit, readiness and transparency pay off in trust and speed to market.
Lab teams appreciate when things “just work,” and that sense comes from foundation pieces like well-prepared intermediates. This reliability isn’t glamourous or headline-grabbing, but it keeps progress moving. That’s the kind of institutional knowledge that makes the difference between a team that muddles through and one that leads the field.
Innovation doesn’t rest. As research priorities shift and regulatory requirements get tougher, attention turns to versatility and scalability. In public conversations and lab discussions alike, practitioners highlight the value of intermediates that adapt to new challenges.
I’ve watched experts in chemical process design experiment with new catalysts and reaction conditions that push even trusted molecules like 5-chloropyridine-3-carbonitrile in new directions. Some teams are piloting continuous manufacturing and integrated in-line monitoring, using this intermediate as a test case for better control and more responsive production.
Other research directions focus on lowering the environmental footprint, adjusting synthetic routes to minimize hazardous waste and energy consumption. Through incremental improvement—sometimes just a new solvent or purification step—real gains show up over time.
Regulatory bodies also keep raising expectations. Compounds with track records of clean reactivity and safe handling make the compliance process smoother. No one wants to return to the days of slow-moving filings and surprise audits. In my view, 5-chloropyridine-3-carbonitrile fits well with the new wave of expectations: flexible, reliable, and compatible with current compliance trends.
Each project brings its own surprises, and no intermediate will fix every challenge. Yet, from firsthand experience, starting out with 5-chloropyridine-3-carbonitrile builds confidence for projects in tough, changeable conditions. Troubleshooting reduces dramatically, and the team spends less time on contingency planning and more on pushing the limits of what’s possible.
During a recent multi-site project, teams using this intermediate ran fewer laboratory-scale repeats and faced fewer surprises during scale-up. Clean analytical readouts and reliable downstream reactivity kept timelines on track, and resource allocation shifted from fixing problems to innovating new solutions. I’ve come to rely on this kind of performance not as a luxury, but as the expectation for forward-thinking R&D and fast-paced commercial launches.
New generations of scientists and engineers are entering a landscape marked by fast change, tighter regulations, and the constant drive for more sustainable products. My advice to anyone aiming at process efficiency or product reliability is to treat the choice of intermediates as a strategic decision, not just a sourcing matter.
By looking beyond price tags and headline specs—by asking about supply chain resilience, process safety, and real-world usability—you’ll find that 5-chloropyridine-3-carbonitrile meets demands not just for today, but for what’s coming next. Teams that recognize and capture this advantage will stand on firmer ground as they take on tomorrow’s projects and challenges.
At the end of the day, great chemistry depends on great building blocks. In my experience, intermediates like 5-chloropyridine-3-carbonitrile are more than numbers and nomenclature—they’re partners in creation, helping convert ideas on paper into valuable products. It’s that dependability and flexibility that leave a mark, long after a project wraps up and the lab lights flicker out.