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HS Code |
795610 |
| Chemical Name | 2-Chloropyridine-4-carbonitrile |
| Molecular Formula | C6H3ClN2 |
| Molecular Weight | 138.56 g/mol |
| Cas Number | 13965-90-7 |
| Appearance | White to light yellow solid |
| Boiling Point | 271 °C (estimated) |
| Melting Point | 76-78 °C |
| Density | 1.32 g/cm3 (estimated) |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | C1=CN=C(C=C1Cl)C#N |
| Inchikey | ANBTYJHESQAYEL-UHFFFAOYSA-N |
| Flash Point | 119.2 °C (estimated) |
As an accredited 2-chloropyridine-4-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle, 25g; tightly sealed with a screw cap; labeled with chemical name, CAS number, hazard symbols, and supplier information. |
| Container Loading (20′ FCL) | 20′ FCL container can load approximately 12 metric tons of 2-chloropyridine-4-carbonitrile, securely packed in sealed drums or bags. |
| Shipping | 2-Chloropyridine-4-carbonitrile is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. Transport complies with relevant hazardous materials regulations, ensuring proper labeling and documentation. Handle with gloves and protective wear; shipping may involve UN-approved packaging, as this chemical requires careful handling due to its toxic and irritant properties. |
| Storage | 2-Chloropyridine-4-carbonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of heat or ignition. Keep it isolated from incompatible substances such as strong oxidizers and acids. Store in a chemical storage cabinet designed for hazardous or toxic organic chemicals, and ensure proper labeling to avoid accidental misuse. |
| Shelf Life | 2-Chloropyridine-4-carbonitrile typically has a shelf life of 2–3 years when stored in a cool, dry, and sealed container. |
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Purity 98%: 2-chloropyridine-4-carbonitrile with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product consistency. Melting point 95°C: 2-chloropyridine-4-carbonitrile meeting a melting point of 95°C is used in agrochemical manufacturing, where controlled melting behavior optimizes process efficiency. Molecular weight 138.55 g/mol: 2-chloropyridine-4-carbonitrile with a molecular weight of 138.55 g/mol is used in heterocyclic compound production, where predictable mass balance facilitates precise formulation. Particle size <50 µm: 2-chloropyridine-4-carbonitrile with a particle size of less than 50 µm is employed in fine chemical blending, where enhanced dispersion improves reaction uniformity. Stability temperature up to 150°C: 2-chloropyridine-4-carbonitrile stable up to 150°C is used in high-temperature synthesis, where it maintains chemical integrity and prevents decomposition. |
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Chemists and researchers working with specialty molecules often find themselves searching for building blocks that keep reactions on track and final products consistent batch after batch. 2-Chloropyridine-4-carbonitrile stands out in this landscape as a compound with a focused molecular structure that delivers reliable performance in the synthesis of pharmaceuticals, agrochemicals, and advanced materials. Structurally, it brings together a chlorinated pyridine core with a nitrile group attached at the fourth position. This mix of functional groups opens up some useful chemistry, not just for academic pursuits, but for real-world industrial applications where consistency and purity count.
Digging into the structure, you notice the chlorine atom snugged onto the second position of the six-membered ring. This chlorine pulls electron density, changing the reactivity across the ring. The nitrile at position four, with its triple-bonded carbon and nitrogen, acts as a versatile handle for modification, especially when crafting more complex molecules. Based on my time in organic synthesis labs and talking with working chemists, a lot of people care about how predictable a molecule behaves. With this compound, reactions like nucleophilic aromatic substitution or palladium-catalyzed cross-couplings tend to go where you expect, thanks to the way the electron distribution encourages or discourages certain steps.
What draws many industrial buyers and development scientists to 2-chloropyridine-4-carbonitrile isn’t just its name or the mere fact of its molecular formula (C6H3ClN2). They pay close attention to its physical form, melting point, and purity. Most suppliers offer it as an off-white to pale-yellow crystalline solid. The melting point typically sits in a narrow range, hinting at controlled crystallization and minimal impurities. Analytical methods such as NMR, mass spectrometry, and HPLC provide real quality assurance by confirming identity and purity; this removes a lot of guesswork during scale-up or QC.
This level of detail matters. Many years ago, I saw firsthand what happens when a batch of a similar pyridine derivative came with only 98% purity instead of the 99% promised on the label. Nobody’s chromatography column lasted more than a couple runs, the product streaked during analysis, and downstream conversions suffered increased side product formation. Teams wound up spending extra time and money cleaning up the mess. With 2-chloropyridine-4-carbonitrile, trusted suppliers know that a tight spec is non-negotiable, not a marketing extra.
Ask a handful of R&D chemists what they’re doing with 2-chloropyridine-4-carbonitrile and you’ll get a mix of answers. Many will talk about pharmaceutical development. This compound forms a strategic piece in the construction of bioactive molecules, especially where a functionalized pyridine backbone appears in the target drug. Its reactivity lets researchers add more groups, swap out the chlorine for other substituents, or transform the nitrile into amines, acids, or other moieties. Some medicinal chemistry campaigns need dozens of slightly different side chains attached to a common core, and here, having a good supply of this intermediate means reactions can run side-by-side with fewer surprises.
Beyond pharma, crop protection scientists also incorporate 2-chloropyridine-4-carbonitrile when designing new agrochemical agents—herbicides, fungicides, or insecticides with pyridine skeletons. As climate conditions and resistance patterns force constant tweaking of molecular structures, intermediates with reliable reactivity and manageable handling properties become even more valuable. You don’t want to waste hours troubleshooting a stubborn intermediate just when pest resistance data demands a fast response.
On the materials front, this compound sometimes crops up in advanced dyes, pigments, and specialty polymers. It may seem niche, but engineers who work on electronic materials or optical brighteners sometimes select pyridine-based units for their electronic characteristics and chemical robustness. Each downstream application values the repeatable behavior of the starting intermediate. No one wants headaches from lots packed with hidden byproducts.
Anyone familiar with heterocyclic chemistry knows the market isn’t short on pyridine derivatives or even on chlorinated nitrile-pyridines. So, what makes the 2-chloro-4-cyano arrangement special? I see two points. One: the placement of the chlorine and nitrile matters a lot more than you’d think. Isomers like 3-chloropyridine-4-carbonitrile or 2-chloropyridine-3-carbonitrile exist, but they don’t react the same. Switching a group from one position to another can kill a synthetic route or launch unexpected side reactions. I once watched a promising scale-up grind to a halt because a positional isomer couldn’t be persuaded to react under the planned conditions. Chemists stick to 2-chloropyridine-4-carbonitrile because they know what it will do and what it won’t, even under challenging lab conditions.
Two: compared to plain 2-chloropyridine or pyridine-4-carbonitrile (where you only get one of these two groups on the ring), the dual-functionalized version opens the door to more elaborate chemistry without an extra round of protection/deprotection steps. Both time and cost savings play out here, especially at scale. I remember a process chemist grumbling about “double work” every time he had to tack on a nitrile or chlorine two steps down the line. Using the right starting intermediate sidesteps lots of grunt work, and in regulated fields, even a modest boost to efficiency can shave months off a development timeline.
Purity shouldn’t be an afterthought, and for 2-chloropyridine-4-carbonitrile, this is where experience pays off. Impurities—especially residual tars, trace metals, or solvent residues left after synthesis—can upset every step downstream. Customers with process chemistry backgrounds watch for color, odor, and solubility clues when opening a new drum. Even reputable suppliers sometimes face criticism when a batch smells off or clumps during storage; these problems hint at micro-decomposition or incomplete drying.
Here’s where strong supplier relationships and regular third-party analysis step up. In practice, I’ve seen experienced procurement folks check old QC data before greenlighting a large purchase. Fact-based decision making staves off waste, keeps operations running, and reassures regulatory folks that compliance standards won’t fall through the cracks. Even minor solubility issues can cause real trouble—one improperly dried lot can jam an automated feeder on the pilot plant floor, halting the whole production run.
Although 2-chloropyridine-4-carbonitrile isn’t known for wild reactivity under most lab conditions, that doesn’t mean you should be careless. Its stability makes storage relatively straightforward. Most users keep it sealed, away from moisture and light, in a cool area. This avoids most degradation, and minimizes nuisance issues such as caking. Larger operations sometimes invest in climate-controlled stores. It might feel like overkill, but I’ve witnessed small savings on energy lead to much larger losses in spoiled inventory—once you see a caked drum exfoliate layer after layer of questionable product, you get more careful about warehouse protocols.
From a safety angle, users should still heed guidelines shared with many chlorinated heterocycles. While acute toxicity generally stays low under normal handling, prolonged or careless exposure (by inhalation or skin contact) isn’t smart policy. Most workflow setups I’ve seen adopt a belt-and-suspenders approach—nitrile gloves, splash-proof eyewear, and local exhaust. I’ve never met a chemist who regretted keeping personal protection high on the priority list.
In my years following chemical market cycles, I’ve noticed few things unsettle specialty synthesis projects more than interruptions in the supply chain. For compounds like 2-chloropyridine-4-carbonitrile, availability depends on access to precursor chemicals and on-site reactor capacity. Some manufacturing sites emphasize backward integration, producing their own chlorinated intermediates, while others rely on third-party suppliers for upstream raw materials. Disruptions—whether from geopolitical shifts, shipping delays, or regulatory changes—ripple through to customers quickly.
From direct experience, some multinational companies build redundancy into their sourcing plans, vetting multiple suppliers and scheduling regular audits. This practice minimizes risk, especially for projects with regulatory deadlines or time-sensitive contracts. Despite the push for global efficiency, a surprising number of buyers now value a certain "semi-local" supply buffer—favoring suppliers who can guarantee restock with minimal lag. During the pandemic, several large buyers scrambled to plug sourcing gaps when shipments got stuck in port or export controls locked down raw materials. A few suppliers with more granular control over their supply lines delivered faster and ultimately retained their customers even post-crisis.
Responsible suppliers of 2-chloropyridine-4-carbonitrile operate under robust quality management systems that support traceability and quick problem-solving. Years ago, I saw a QC lab head at a mid-sized specialty manufacturer explain how regular method validation—using international guidelines—helped catch subtle drifts in product quality early. Customers then noticed fewer “bad batch” complaints. Raw material traceability allowed quick root-cause investigations whenever something slipped. Suppliers who take this task seriously cultivate trust, and in regulated industries, trust isn’t built overnight.
End users also play a role in reinforcing quality standards by requesting supporting documentation (certificates of analysis, stability data, impurity profiles) and following up if discrepancies arise. A couple of researchers told me how an open dialogue with their suppliers helped solve a recurring issue with moisture content. Instead of hiding behind paperwork, the supplier proactively improved packaging, cutting down on complaints and improving user satisfaction all around.
The world of specialty chemicals isn’t immune from pressure to cut waste, shrink footprints, and demonstrate stewardship beyond compliance. 2-Chloropyridine-4-carbonitrile, as an intermediate, interacts with these expectations at every stage. Green chemistry trends push process engineers to minimize waste, look for recyclable solvents, and scale up reactions that run cleaner. Many academic and industrial chemists now publish greener methods for making pyridine derivatives, with a focus on milder conditions, less hazardous reagents, or recyclable catalysts. These efforts might not always get center stage on company brochures, but inside project meetings, sustainable improvements push projects above the line.
Waste handling for pyridine-based intermediates also gets attention. Some facilities invest in on-site incineration or advanced wastewater treatment to catch traces of organic contaminants before release. The cost difference isn’t trivial, but the reputational risk of taking shortcuts can haunt companies for years. I remember a client who spent time and resources reworking their entire solvent system to cut persistent contamination in their effluent streams. Far from just a PR exercise, those efforts made audits go smoother and opened doors to bigger customers demanding tighter environmental controls.
The versatility of 2-chloropyridine-4-carbonitrile as a chemical building block helps move both established and emerging research in a number of directions. In drug discovery and development, chemists often work through multiple pathways, exploring how subtle modifications influence bioactivity or metabolism. Here, confidence in the behavior of a core intermediate means researchers can focus on the biology, not troubleshooting constant synthetic snags.
In my own work with interdisciplinary teams, projects sometimes rose or fell on the timely delivery and performance of foundational intermediates like this one. Delays caused by poor handling, missed specifications, or questionable supply set back not only lab schedules but also patent filings and regulatory documentation. Consistent, transparent supply keeps not just the beakers bubbling, but the entire innovation machine moving at pace.
Attend any conference session focused on synthetic intermediates and the real stories come out: successes, disasters, and improvements driven by shared experience. Peers swap details about reaction conditions, yields, and even quirks noticed during storage. This sharing culture shapes product selection every bit as much as glossy brochures.
I’ve heard about teams discovering that using slightly different grades of 2-chloropyridine-4-carbonitrile, each from distinct suppliers, shook up their reaction results. Some versions ran cleaner; others delivered unexpected byproduct profiles. Rather than relying on hearsay, most researchers now publish supporting data or openly compare notes, helping the broader community make more informed choices. Such transparency, backed by real-world data, amplifies confidence in purchase decisions and process improvements.
For buyers and users who want to avoid familiar pitfalls—late deliveries, inconsistent performance, or hidden impurities—several concrete steps can help. Multi-supplier sourcing strategies make a difference. So does regular third-party testing, even for lots from trusted partners. Building relationships with vendors who provide not only a product but also robust customer support makes trouble-shooting issues much easier. When a supply hiccup arises or a technical question crops up, a responsive supplier helps sidestep delays.
On the technical side, investing in staff training pays off. When chemists and QC analysts know how to spot subtle shifts in product appearance or analytical outputs, small issues don’t balloon into major setbacks. Modern analytical tools—NMR, HPLC, ICP-MS—are essential, but hands-on experience cannot be automated. In environments where timelines matter, knowledge transfer between older and younger generations of chemists keeps best practices alive.
Process optimization and standardization, while sometimes glossed over, form a backbone for large-scale users. A standardized workflow reduces the odds of mistakes, missed steps, or variability that creeps in unnoticed. A few organizations now lean on digital batch tracking and real-time analytics to spot abnormalities as soon as they start. This minimizes the chance of a bad lot sneaking through to production.
As pharmaceutical, agrochemical, and material science projects grow in complexity, the demand for versatile, pure, and dependable intermediates like 2-chloropyridine-4-carbonitrile will keep rising. This isn't speculation; it's grounded in the reality that every new molecular scaffold, every fresh lead compound, often relies on a series of robust, nuanced building blocks. End users, from bench chemists to procurement officers, continue to ask more from their supply partners—transparent processes, greener methods, and steady support.
Unlike some molecule-of-the-month chemicals, 2-chloropyridine-4-carbonitrile maintains a steady relevance in a field that’s always pushing new frontiers. Its significance rests not just in reactive moieties, but in proven performance and adaptability to changing needs. Whether in a high-throughput discovery project or a carefully optimized production setting, the value lies as much in trust as in technicality.
Looking back at years of navigating chemical libraries and supplier lists, I’ve seen how one dependable intermediate can help ambitious research and complex manufacturing keep pace with real-world demands. 2-Chloropyridine-4-carbonitrile serves as a reminder that proven performance, handled with care and supported by clear communication, makes all the difference. The most successful teams are those that match technical expertise with practical problem solving, staying vigilant about the quality and reliability of their key materials.
Open dialogue with both suppliers and users, commitment to regular quality checks, and a willingness to tweak processes in response to hard data create an environment where challenges can turn into breakthroughs. As the world of chemistry faces new pressures—from supply chain disruptions to regulatory scrutiny—those invested in both technical excellence and transparency will carve out ongoing opportunity.
2-Chloropyridine-4-carbonitrile isn’t another faceless entry in a catalog; it’s a testament to how choice, reliability, and collaboration shape the journeys from discovery to scaled production. Those who work with it know that thoughtful selection and consistent attention to detail ripple outward, influencing far more than one reaction or one product line. It has grown into a staple of modern synthesis for good reason—and as technology and application areas evolve, its relevance looks set to continue.