|
HS Code |
180786 |
| Chemical Name | 4-Chloro-2-pyridinecarbonitrile |
| Molecular Formula | C6H3ClN2 |
| Molar Mass | 138.56 g/mol |
| Cas Number | 3430-16-8 |
| Appearance | White to light yellow crystalline powder |
| Melting Point | 73-77 °C |
| Boiling Point | 283-285 °C |
| Density | 1.31 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 126.9 °C |
| Smiles | C1=CC(=NC=C1Cl)C#N |
| Inchi | InChI=1S/C6H3ClN2/c7-5-1-2-8-6(3-5)4-9 |
| Synonyms | 4-Chloro-2-cyanopyridine |
As an accredited 4-CHLORO-2-PYRIDINECARBONITRI& factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for 4-Chloro-2-pyridinecarbonitrile (25g) is a sealed amber glass bottle with a secure screw cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-Chloro-2-pyridinecarbonitrile typically involves 10–12 MT packed in 25 kg fiber drums or bags. |
| Shipping | 4-Chloro-2-pyridinecarbonitrile is shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It is handled as a hazardous material, commonly shipped via ground or air freight with appropriate labeling in accordance with local, national, and international transport regulations (such as DOT, IATA, or IMDG), typically under UN hazardous goods guidelines. |
| Storage | **Storage Description for 4-Chloro-2-pyridinecarbonitrile:** Store in a cool, dry, and well-ventilated area away from sources of ignition and incompatible materials such as strong oxidizers. Keep the container tightly closed and protect from moisture and direct sunlight. Use appropriate chemical-resistant containers and ensure clear labeling. Follow all standard safety protocols for handling hazardous organic chemicals. |
| Shelf Life | Shelf life of 4-chloro-2-pyridinecarbonitrile: Typically stable for 2–3 years when stored tightly sealed at 2-8°C, away from moisture. |
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Purity 98%: 4-CHLORO-2-PYRIDINECARBONITRI& with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield of target compounds. Melting Point 49-53°C: 4-CHLORO-2-PYRIDINECARBONITRI& with melting point 49-53°C is used in organic reaction processes, where it facilitates precise thermal control during synthesis. Molecular Weight 138.55 g/mol: 4-CHLORO-2-PYRIDINECARBONITRI& with molecular weight 138.55 g/mol is used in agrochemical formulation, where it provides consistency in active ingredient calibration. Particle Size <20 μm: 4-CHLORO-2-PYRIDINECARBONITRI& with particle size <20 μm is used in fine chemicals manufacturing, where it improves homogeneity in blends. Stability Temperature up to 120°C: 4-CHLORO-2-PYRIDINECARBONITRI& with stability temperature up to 120°C is used in industrial synthesis procedures, where it ensures reliable performance under elevated conditions. Residual Moisture <0.5%: 4-CHLORO-2-PYRIDINECARBONITRI& with residual moisture <0.5% is used in API production, where it minimizes unwanted side reactions. Solubility in DMF: 4-CHLORO-2-PYRIDINECARBONITRI& with high solubility in DMF is used in heterocyclic compound preparation, where it enables efficient dissolution and reaction kinetics. Assay ≥99%: 4-CHLORO-2-PYRIDINECARBONITRI& with assay ≥99% is used in laboratory-scale medicinal chemistry, where it guarantees reproducibility in experimental outcomes. |
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4-CHLORO-2-PYRIDINECARBONITRILE, with the molecular formula C6H3ClN2, belongs to the broader family of chloropyridine compounds and nitriles. At first glance, its chemical name may sound like just another identifier out of a list. For researchers and professionals who work with chemical synthesis, 4-CHLORO-2-PYRIDINECARBONITRILE is more than a formula — it’s a reliable intermediate that helps push boundaries in pharmaceutical manufacturing, crop protection, and advanced materials. The appeal of this molecule lies in its well-defined reactivity, purity, and the versatility brought by the union of a pyridine ring with a nitrile and a chlorine substituent.
Chemistry has a reputation for complexity, but day-to-day innovation depends on molecules like this one. In the pharmaceutical sector, labs look at 4-CHLORO-2-PYRIDINECARBONITRILE as a scaffolding component. Medicinal chemists often use it to build new drug candidates, tweak lead compounds, or test out different ring modifications for better receptor binding or metabolic stability. It acts as a starting point in the construction of benzodiazepine derivatives, kinase inhibitors, or anti-infective agents. If you've ever seen the leap from rational drug design on a computer screen to a vial of sample molecules, you'd see how much groundwork rests on reliable intermediates.
In the agrochemical arena, sturdy molecules translate into better crop yields and pest management. 4-CHLORO-2-PYRIDINECARBONITRILE brings a certain advantage in crafting herbicides and fungicides. Its structure meshes well in ring construction processes, making it an attractive precursor for active agrochemical ingredients. I’ve seen research projects where subtle changes in the position of the chlorine or nitrile group made the difference between a highly active product and a non-starter. Since crop threats evolve quickly, researchers count on molecules that allow for fast adaptation and have ok environmental profiles.
Material science represents another outlet. The unique electronic impacts of chlorine atoms and nitrile functionality bring value in synthesizing organic electronics, high-performance polymers, and specialty coatings. Thin-film semiconductors or novel colorants sometimes need core molecules that withstand stress and resist breakdown. In these projects, even a reliable intermediate can become quietly essential.
Attention to detail matters from early-stage discovery to final product preparation. As with many specialty chemicals, the specifications behind 4-CHLORO-2-PYRIDINECARBONITRILE set the expectations for every batch. Chemists care about purity — usually upwards of 98 percent — for reliable reactions, trace metals below a few parts per million, and absence of interfering byproducts like 2-cyanopyridine or 4-chloropyridine. Slight shifts in impurity profiles create headaches during separations or when aiming for high-value targets with strict regulatory requirements.
Batch-to-batch consistency, moisture content, and control over particle size become more valuable with scale-up. Having a supplier who hits these key marks and can provide third-party analytical documentation relieves pressure at the downstream stages, whether it’s route scouting or process validation.
In my experience, taking shortcuts on traceability or purity does not pay off. Years ago, I witnessed a scale-up project derail from what looked like a barely detectable impurity in a pyridine intermediate. Only a handful of parts per million, but the trouble rippled through a synthesis and showed up during the final crystallization step — lost time, wasted resources, dashed deadlines.
With strict regulatory frameworks in pharma and food-adjacent chemistry, it’s good practice to demand certificates of analysis and a transparent supply chain. If your product finds its way into an active ingredient or a regulated additive, audit trails back to the starting materials tend to be non-negotiable.
People sometimes lump pyridine derivatives together, but structure dictates performance. 4-CHLORO-2-PYRIDINECARBONITRILE sits apart from plain 2-cyanopyridine or derivatives with chlorine in other positions. Shifting a chlorine substituent on the aromatic ring can alter electron distribution, steric profile, and reactivity in follow-up chemistry.
For certain transformations — say, Suzuki couplings or nucleophilic substitutions — activation patterns open or close routes depending on where the chlorine lives. For example, a 3-chloro derivative generally resists some substitution methods, while the 4-chloro structure welcomed new partners in published work. If your synthesis plan calls for specific bond formation, the choice between these is not just academic but can define success or failure.
Compare this compound with the more widely used 2-chloropyridine or 3-chloropyridine derivatives. Each offers a different blend of selectivity, toxicological profile, and downstream modification options. Some projects need a chlorine group further from the nitrile to reduce side reactions or to steer regioselectivity. Others depend on the balance of hydrophobicity and polar sites to optimize binding or biological uptake. Even small molecular tweaks send ripples through process chemistry and finished product performance.
Experience tells me that the safest and most efficient processes come from careful planning and straightforward practices. 4-CHLORO-2-PYRIDINECARBONITRILE, packed in airtight, light-resistant containers, fares best in dry, cool storage — just like most sensitive aromatic nitriles. Those containers often look unremarkable, but they are there to avoid unwanted hydrolysis, clumping, or accidental moisture uptake. In larger settings, workers depend on a solid culture of label integrity, secure seals, and regular rotation.
As for handling, most facilities require gloves, goggles, and standard PPE — for good reason. Any pyridine compound carries risk if inhaled, ingested, or splashed. Occasional pungent odors and the skin-sensitizing potential remind me, and others, never to drop our guard around fine chemicals, no matter how routine the operation.
Stories about disrupted shipments and unpredictability in chemical supply chains have grown more common over recent years. Lack of easy access to intermediates such as 4-CHLORO-2-PYRIDINECARBONITRILE can hobble both small, agile firms and multinational producers. The reasons range from regulatory shifts, erratic demand cycles, or changes in environmental rules governing plant emissions. Manufacturers sometimes switch solvents, catalysts, or purification techniques depending on local policies, which in turn feedback into the impurity landscape and batch quality.
If I had to share one idea from the past decade, it would be the value of fostering redundant supplier relationships and keeping open lines of communication about origin, process changes, or capacity limits. Building a resilient network can head off expensive emergencies. Even well-meaning intermediaries can introduce delays by trying to smooth over batch quality swings, jeopardizing R&D timelines or scaling-up phases.
The topic of sustainable chemical manufacturing often drifts toward mottos, but there’s substance behind the movement for greener procedures. For 4-CHLORO-2-PYRIDINECARBONITRILE and its kin, alternative synthetic routes receive regular scrutiny. From academic literature to pilot plant reports, solvent substitution, catalyst recycling, and reduced-waste workups aim to make even niche chlorine chemicals less resource-intensive.
Occasionally, innovation lags in specialty chemicals because volumes are small compared with, say, commodity plastics or fuels. Still, regulatory guidelines and customer audits create pressure to tighten emissions, manage spent reagents, and anticipate lifecycle issues. Firms bringing this molecule to market who prove compliance with environmental standards or offer recycled solvent origins tend to stand out in the eyes of buyers juggling compliance and ESG goals.
Beyond synthesis, choices about secondary packaging, batch labeling, or shipping go hand in hand with rising expectations for low-waste protocols. For buyers committed to zero landfill or carbon-neutral operations, the finer points — pallet composition, drum recycling, shipping manifests — have become selling points, not afterthoughts.
Discussion about specialty intermediates is incomplete without a clear acknowledgment of safety and regulatory risk. 4-CHLORO-2-PYRIDINECARBONITRILE, while not as infamous as some halogenated aromatics, falls under reach and other chemical registration laws in most developed regions. Hazard communication standards, original MSDS access, packaging in compliance with GHS labeling, and dedicated spill kits in receiving areas are not just paperwork but parts of a robust risk management system.
Regular staff training, clear signage, and standard operating procedures help smooth operations, especially when the team shifts or outside contractors rotate through. I can recall a case where unfamiliarity with nitrile intermediate hazards led to near-miss exposure. In short, sharp focus on safety matters, not just meeting the letter of regulation, but because day-to-day productivity rises once people aren’t second-guessing their basic instructions.
From startup incubators to large-scale pharmaceutical operations, innovation depends on tools that deliver flexibility and reliability. 4-CHLORO-2-PYRIDINECARBONITRILE often plays an unheralded role in this mix. Its reactivity allows medicinal chemists to try out new motifs, bridge different functional groups, and chase “orthogonal” reaction routes inaccessible with more generic pyridines. In the crop science labs, a single intermediate can enable the creation or testing of dozens of lead analogs in a short time.
Year after year, I see consistency emerge as a major advantage. The right intermediate — available, high quality, with solid documentation — allows for faster troubleshooting, smarter process development, and easier regulatory submissions. Projects falter not because of breakthroughs that never materialize, but because the basics went missing. Reliable building blocks keep the gears turning.
Market analysis reports confirm that the global pyridine derivatives sector keeps expanding, with specialty intermediates contributing to both volume and profitability. Growth in demand for new active pharmaceutical and agrochemical ingredients means that robust supply chains and new synthetic strategies gain traction each year. Peer-reviewed publications document the dependence on high-purity pyridine intermediates for enantioselective synthesis, bioconjugation ventures, and the tweaking of physical properties in electronic applications.
Over the past five years, academic groups have published strategies for more atom-economical and less energy-intensive syntheses of pyridine nitriles with chlorine. These approaches, as shown in recent American Chemical Society articles, reduce the burden of waste handling and hazardous byproducts. Equipment upgrades, batch process intensification, and remote monitoring play their role in raising the efficiency bar.
Despite the promise, certain hurdles remain in deploying 4-CHLORO-2-PYRIDINECARBONITRILE in newer or smaller settings. Cost can be non-trivial when compared with more common intermediates, especially when factoring in transportation and customs procedures for controlled chemicals. For some R&D projects, the perceived complexity of registration or unfamiliarity with the specific reactivity profile keeps people sticking with older, less versatile molecules.
One common misstep is underestimating the degree of formulation or route optimization possible with this intermediate. Labs sticking too closely to legacy methods or bulk commodity chemistry practices might overlook solutions involving the selective use of 4-CHLORO-2-PYRIDINECARBONITRILE. Conferences and technical exchanges show time and again that peer networks drive adoption — hearing case stories from colleagues makes the difference for cautious managers considering an initial purchase or new method.
Knowledge sharing and reliable technical guidance speed up the learning curve. Strong supplier partnerships open the door to troubleshooting support, sharing analytical expertise, and benchmarking batch consistency against industry leaders. More firms now publish method notes, synthesis apps, and suggested use cases for popular intermediates — all making life easier for the in-house teams faced with tight deadlines and pressure for faster development cycles.
Scaling up from bench to kilo or pilot plant batches presents its own challenges, especially around exothermicity, heat management, and waste handling. Consulting with process chemists who have made errors in temperature control or vented hazardous vapors will drive home the importance of process simulation and HAZOP review. In addition, supply chain digitization and vendor management software reduce miscommunications about certification or lead times, which in turn aids smoother integration.
Resilient procurement means not relying solely on the lowest-cost supplier but weighing years-in-business, lab accreditation, complaint response, and transparency in raw materials sourcing. This intermediate, like others with sensitive functional groups, rewards long-term, value-based relationships that go past invoice and delivery schedules toward joint problem-solving.
For those working at the bench, every new lot of 4-CHLORO-2-PYRIDINECARBONITRILE brings a combination of anticipation and careful diligence. All it takes is a single batch deviation to muddy spectral signatures or throw off downstream purifications. Remembering that synthetic targets rest on the shoulders of reliable building blocks brings a sense of respect for the long supply chains and labor hours leading up to every bottle.
The hands-on aspect of chemistry stands out particularly vividly here. Smell, color, weight, and solubility — all go through real-world validation before the first reaction setup. Problems caught upfront by vigilant techs or process chemists often prevent costly setbacks later, and the details recorded in lab notebooks become valuable resources for the next round of optimization.
Ultimately, the value in a compound such as 4-CHLORO-2-PYRIDINECARBONITRILE flows not just from its chemical reactivity, but from everything tied to its stewardship: knowledge, communication, safety, and a respect for how precise details move science forward.