2-Chloropyridine-5-carbonitrile

    • Product Name: 2-Chloropyridine-5-carbonitrile
    • Chemical Name (IUPAC): 5-chloropyridine-3-carbonitrile
    • CAS No.: 4546-17-0
    • Chemical Formula: C6H3ClN2
    • Form/Physical State: Powder
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    466804

    Chemical Name 2-Chloropyridine-5-carbonitrile
    Molecular Formula C6H3ClN2
    Molecular Weight 138.56 g/mol
    Cas Number 34941-53-2
    Appearance White to light yellow solid
    Melting Point 62-65 °C
    Boiling Point 307 °C
    Density 1.38 g/cm³
    Solubility In Water Slightly soluble
    Purity Typically ≥98%
    Smiles C1=CC(=NC(=C1)Cl)C#N
    Inchi InChI=1S/C6H3ClN2/c7-6-2-1-5(3-8)4-9-6/h1-2,4H
    Storage Conditions Store in a cool, dry, well-ventilated place
    Synonyms 2-Chloro-5-cyanopyridine

    As an accredited 2-Chloropyridine-5-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2-Chloropyridine-5-carbonitrile is packaged in a 25g amber glass bottle with a secure screw cap and clear labeling.
    Container Loading (20′ FCL) Container loading (20′ FCL) for 2-Chloropyridine-5-carbonitrile ensures secure, moisture-free, and compliant bulk chemical transport in sealed drums.
    Shipping 2-Chloropyridine-5-carbonitrile is shipped in tightly sealed containers to prevent moisture and contamination. It should be handled as hazardous material according to standard chemical transport regulations. The package must display appropriate hazard labels and be stored in a cool, well-ventilated area during transit to ensure chemical stability and safety.
    Storage 2-Chloropyridine-5-carbonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of heat and ignition. Protect it from moisture and incompatible substances, such as strong oxidizers. Store at room temperature and ensure the area is equipped with proper spill control measures. Keep away from direct sunlight and use only in chemical fume hoods.
    Shelf Life 2-Chloropyridine-5-carbonitrile typically has a shelf life of 2–3 years when stored in a cool, dry, and airtight container.
    Application of 2-Chloropyridine-5-carbonitrile

    Purity 99%: 2-Chloropyridine-5-carbonitrile with purity 99% is used in pharmaceutical intermediate synthesis, where it enables high-yield and low-impurity product formation.

    Melting point 72°C: 2-Chloropyridine-5-carbonitrile with a melting point of 72°C is used in agrochemical development, where it facilitates easy integration into solid formulation processes.

    Particle size <20 μm: 2-Chloropyridine-5-carbonitrile with particle size less than 20 μm is used in fine chemical manufacturing, where it ensures homogeneous mixing and improved reaction kinetics.

    Moisture content <0.5%: 2-Chloropyridine-5-carbonitrile with moisture content below 0.5% is used in catalyst production, where it maintains catalyst activity and prevents hydrolysis.

    Molecular weight 152.56 g/mol: 2-Chloropyridine-5-carbonitrile with a molecular weight of 152.56 g/mol is used in heterocyclic compound synthesis, where it offers accurate molar conversions for reproducible batch control.

    Stability temperature up to 160°C: 2-Chloropyridine-5-carbonitrile with stability up to 160°C is used in high-temperature organic synthesis, where it minimizes decomposition and enhances product yield.

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    Certification & Compliance
    More Introduction

    Introducing 2-Chloropyridine-5-carbonitrile: A Practical Compound Changing the Game in Chemical Synthesis

    A Hands-On Look at 2-Chloropyridine-5-carbonitrile

    Having worked with specialty chemicals over the years, a compound like 2-Chloropyridine-5-carbonitrile tends to stand out for those in the know. Colleagues in research labs usually nod in respect when they spot it on a supplier’s list, since this molecule bridges a pesky gap in pyridine chemistry that comes up in medicinal development and advanced materials. The molecular structure—featuring a chlorine atom at the two position, a nitrile group at the five—offers a combination of reactivity and selectivity that’s tough to match. This means more direct routes in making complex organic molecules for those tinkering with pharmaceuticals or agrochemicals.

    Working in a small drug discovery team, I’ve found that reliable intermediates save hours of troubleshooting. The compound’s purity, often hitting a solid 98% or above, helps keep downstream reactions clean. Contaminants and byproducts can wreck expensive reagents or force one too many column chromatography steps. That’s partly why this chemical draws a steady stream of customers from both large and nimble organizations.

    Specifications That Matter for the Lab and Industry

    2-Chloropyridine-5-carbonitrile comes as an off-white to light-yellow solid, sometimes sold in crystalline or powder form. The melting point hovers around 85-88°C. In terms of solubility, the compound blends well with polar aprotic solvents such as DMSO and DMF, and dissolves sparingly in water. These characteristics play a role in how researchers incorporate it into reaction setups.

    Chemists care about specification values because they affect scale-up and reproducibility. I’ve seen analytical reports showing moisture content below 0.5%, with HPLC purity routinely at or above 98%. Knowing precise content of the target molecule lets labs adjust measurements accurately, whether for gram-scale syntheses or pilot lots. These kinds of assurances are key, especially when running parallel experiments—one contaminated batch can skew a whole week’s worth of data.

    Field-Tested Applications Driving Real Innovation

    The biggest draw for 2-Chloropyridine-5-carbonitrile comes from its smooth function as a building block for bigger, more complex compounds. Medicinal chemists frequently use it as a starting point for synthesizing pyridine-based pharmaceuticals. The electronegative chlorine substituent opens up possibilities for nucleophilic aromatic substitution, Suzuki coupling, or other cross-coupling strategies. At the same time, the nitrile group is a door to countless transformations—turning into amines, converting to acids, or serving as an anchor for further modification down the chain.

    In my experience, the flexibility promised on paper translates to the bench. I once worked on a hit-to-lead campaign for kinase inhibitors. We needed a robust scaffold, and 2-Chloropyridine-5-carbonitrile allowed us to rapidly iterate libraries by tweaking both the chloro and cyano sites. Synthetic efficiency leads to shorter timelines, which makes a real difference in tight research budgets. In the agrochemical sector, where cost and time-to-market matter, this compound has also featured in several early-stage discovery programs targeting weed and pest resistance.

    The Differences That Set It Apart

    Comparing 2-Chloropyridine-5-carbonitrile with other chloropyridines or simpler nitriles reveals a few practical advantages. Many chloropyridines lack the cyano group, limiting downstream functionalization. Simple pyridines without halogen substitution often react less selectively, which can result in mixtures and separation headaches. By contrast, the dual presence of chloro and nitrile groups in this molecule means chemists access multiple derivatization pathways—critical for both diversity-oriented synthesis and fine-tuned reaction planning.

    Another key difference shows up in selectivity. Direct substitution at the five position on a pyridine ring isn’t trivial. With both activating and blocking effects from the chlorine and nitrile, unwanted side reactions drop compared to similar scaffolds. Fewer purification steps mean not only cleaner products but less solvent waste and lower overall material costs. Sustainability teams have started noticing these tangibles as regulatory pressures and environmental standards tighten across the industry.

    Real-World Challenges and Sustainable Solutions

    No chemical is free from handling considerations, and 2-Chloropyridine-5-carbonitrile carries its own set of challenges. Like many aromatic nitriles, exposure precautions matter—proper ventilation, gloves, and eye protection are standard for anyone in the lab. Workplaces with robust safety cultures train technicians on correct weighing and disposal. Overcoming these hurdles means developing and sticking to clear operating procedures, a lesson driven home for me after a minor spill that led to unnecessary downtime and paperwork.

    Waste stream management represents another area requiring attention. Pyridine derivatives can be persistent in the environment, so responsible users must look beyond immediate convenience toward minimal waste protocols. Our team invested in solvent-recycling systems and periodic reviews of end-of-life product pathways to lessen ecological impacts. Advances in green chemistry may soon deliver even cleaner synthetic routes for this compound, reducing both hazardous reagents and byproducts.

    Supporting Innovation Across Disciplines

    Chemicals like 2-Chloropyridine-5-carbonitrile play a quiet but central role in expanding research frontiers. As patent literature and published papers continue to grow, more projects feature this versatile building block, either directly or as a stepping stone toward blockbuster molecules. Collaborative partnerships between suppliers and customers have driven improvements in grade, particle size, and documentation standards over recent years.

    Anyone tasked with R&D work in pharmaceuticals, specialty dyes, or crop protection soon learns the value of dependable supply and open communication regarding analysis results. I remember rerouting a project to a new supplier after inconsistent melting points and HPLC traces raised flags—quick turnaround times and document transparency turned a potential delay into a learning opportunity for the whole team.

    Opportunities for Further Progress

    Looking toward the future, researchers have called for more scalable and sustainable preparations of 2-Chloropyridine-5-carbonitrile. While classic routes have proven effective, recent advances have shown promise with catalytic cross-coupling sequences or alternative nitrile installation techniques that use greener conditions. Integrating these pathways on commercial scales could trim costs and reduce chemical footprints industry-wide.

    One area ripe for improvement involves reducing the use of toxic solvents and streamlining purification. Several labs have published new protocols using water-based or lower-toxicity alternatives, alongside continuous flow methods that shrink energy demands. My own attempts at catalyzed couplings using milder bases have left me optimistic about further yield improvements with less waste.

    Quality Assurance: Building Trust with Transparency

    Trust between supplier and end user depends on more than just purity numbers. Full certificates of analysis, spectral data, and method transparency give researchers peace of mind. After all, a single batch discrepancy can sometimes translate into wasted months for complex synthetic sequences. Over time, my confidence in certain suppliers grew after years of consistent results and willingness to answer technical questions—qualities that matter more as regulatory scrutiny rises.

    High standards also extend to packaging and labeling. Properly sealed containers prevent moisture intrusion or oxidation. Barcode tracking and digital documentation streamline inventory management, reducing costly mix-ups in day-to-day operations. These aspects come into play especially when multiple research teams draw from the same stockroom or when materials must be traced through several production stages.

    Real-World Impacts: From Bench to Market

    Beyond the laboratory, the impact of 2-Chloropyridine-5-carbonitrile shows up in improved crop protection products and more effective medications. Some of the next-generation fungicides and insecticides owe their efficacy to pyridine derivatives that stem from this compound. In pharmaceuticals, clearer SAR (structure-activity relationship) matrices arise from systematic substitutions on the pyridine ring, helping deliver better candidates for preclinical testing.

    I’ve seen research teams pivot quickly from promising in vitro results to fully fleshed-out development candidates by leveraging the versatility of such intermediates. Fast, reliable access to specialty chemicals shortens the cycle between hypothesis and measurable impacts, earning the trust of investors and management.

    Why Choosing the Right Compound Matters

    The choice of chemical building blocks shapes the workflow across modern laboratories. Selecting 2-Chloropyridine-5-carbonitrile over less functionalized options brings tangible benefits—greater flexibility in downstream reactions, higher selectivity, cleaner assays, and sometimes, lower waste streams. For students, grad students, and industry veterans alike, early familiarity with this compound opens creative avenues for new synthetic methodologies.

    Over the years, I’ve seen teams struggle through convoluted protection-deprotection schemes when simpler routes based on the right intermediate were at hand. Time and again, investment in high-purity reagents paid off in both labor and material savings. Junior chemists learn quickly that starting with quality ingredients keeps the focus on discovery, not troubleshooting.

    Meeting the Demands of Today’s Changing Landscape

    New regulatory frameworks and shifting public opinion keep raising the bar for chemical safety, provenance, and environmental impact. 2-Chloropyridine-5-carbonitrile suppliers responding to these demands tend to thrive, winning loyalty with tested quality and clear safety protocols. For procurement teams and researchers alike, transparency around source, batch testing, and storage conditions becomes more than just compliance—it signals a genuine investment in customer success.

    Modern facilities often configure their procurement processes around validated supply chains, traceable origin, and integrated quality management. This reflects growing appreciation for the harm that can come from supply disruptions or inconsistent stock. Steady demand across pharmaceuticals and crop science circles suggests that well-documented and responsibly sourced 2-Chloropyridine-5-carbonitrile will keep its position as a sought-after intermediate.

    Tips for Labs and R&D Teams

    Practical advice for researchers thinking of using 2-Chloropyridine-5-carbonitrile centers on starting with reliable technical data and validated protocols. Check spectral analysis reports for each lot, ask questions about shipping timelines, and review safety data before launching multistep sequences. Teams benefit from setting up small-scale piloting ahead of full integration into screening campaigns.

    Maintaining open conversations between research, purchasing, and EHS (environmental health and safety) teams helps avoid bottlenecks and misunderstandings. As many graduate students and postdocs have found, investing attention in reagent quality at the outset often avoids larger problems down the road.

    Contributing to Science and Society

    At its core, 2-Chloropyridine-5-carbonitrile reflects the steady march of scientific progress. Each year, novice and veteran researchers alike put it to the test in new target syntheses, creative molecular modifications, and breakthrough discoveries. Whether helping push a molecule from concept to clinical candidate or providing a stepping stone for next-generation materials, it highlights the value of robust and flexible foundations in chemical synthesis.

    Society ultimately benefits from the quiet reliability of compounds like this—delivering safer medications, greener crop protection agents, and advanced specialty chemicals. As experience has shown time and again, investing in well-understood intermediates paves the way for safer products, higher standards, and lasting contributions across fields.

    Connecting to the Bigger Picture

    My years around research labs drove home one broad truth—progress depends on both inspiration and nuts-and-bolts reliability. The story of 2-Chloropyridine-5-carbonitrile paints a picture of chemical science grounded in practical know-how and ongoing innovation. As long as the need for efficient, cost-effective, and reliable chemical building blocks continues, this compound will keep making a mark in labs and beyond.

    Lessons learned from working with this compound—demanding clear documentation, insisting on quality, and always watching for new greener routes—hold true no matter where one’s career leads. For those planning future discoveries, 2-Chloropyridine-5-carbonitrile stands as a still-relevant and practical tool for the modern chemistry toolkit.