|
HS Code |
215582 |
| Compound Name | 5-Chloro-3-methylpyridine-2-carbonitrile |
| Molecular Formula | C7H5ClN2 |
| Molecular Weight | 152.58 g/mol |
| Cas Number | 15862-28-1 |
| Appearance | White to light yellow solid |
| Melting Point | 70-75°C |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Smiles | CC1=CN=C(C#N)C=C1Cl |
As an accredited 5-Chloro-3-methylpyridine-2-carbonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle with a tightly sealed cap, labeled "5-Chloro-3-methylpyridine-2-carbonitrile, ≥98% purity, batch number, CAS 1122-89-6." |
| Container Loading (20′ FCL) | 20′ FCL: Carries 12 MT of 5-Chloro-3-methylpyridine-2-carbonitrile, packed in 25 kg fiber drums, ensuring safe transportation. |
| Shipping | 5-Chloro-3-methylpyridine-2-carbonitrile is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is transported according to appropriate chemical safety regulations, including proper labeling and documentation. Storage and shipping conditions typically require a cool, dry environment, away from incompatible materials and ignition sources. Handle with standard laboratory safety precautions. |
| Storage | 5-Chloro-3-methylpyridine-2-carbonitrile should be stored in a cool, dry, 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. Standard precautions for handling hazardous chemicals should be observed to prevent exposure or accidental release. |
| Shelf Life | 5-Chloro-3-methylpyridine-2-carbonitrile typically has a shelf life of 2-3 years when stored cool, dry, and tightly sealed. |
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Purity 99%: 5-Chloro-3-methylpyridine-2-carbonitrile with 99% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and API purity. Melting point 95°C: 5-Chloro-3-methylpyridine-2-carbonitrile with a melting point of 95°C is used in agrochemical manufacturing, where it guarantees consistent thermal stability during formulation. Particle size <50 μm: 5-Chloro-3-methylpyridine-2-carbonitrile with particle size below 50 μm is used in catalyst precursor preparation, where it enhances homogeneity in catalytic compositions. Moisture content <0.3%: 5-Chloro-3-methylpyridine-2-carbonitrile with moisture content below 0.3% is used in electronics chemical synthesis, where it minimizes hydrolysis and unwanted side reactions. Stability temperature up to 120°C: 5-Chloro-3-methylpyridine-2-carbonitrile stable up to 120°C is used in custom polymer additive production, where it maintains structural integrity during processing. Assay ≥98.5%: 5-Chloro-3-methylpyridine-2-carbonitrile with assay not less than 98.5% is used in fine chemical development, where it achieves reproducible batch-to-batch quality. Volatile impurities <0.2%: 5-Chloro-3-methylpyridine-2-carbonitrile with volatile impurities under 0.2% is used in dye intermediate synthesis, where it reduces contamination and improves final product consistency. |
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Creating 5-Chloro-3-methylpyridine-2-carbonitrile in our plant isn’t just about chemical conversion—it’s about predictability and securing outcomes in downstream chemistry. Day in and day out, the demand for reliable pyridine intermediates keeps chemists and production supervisors on their toes, especially with so many nuanced changes affecting small molecule synthesis. Our approach to 5-Chloro-3-methylpyridine-2-carbonitrile starts with selecting high-purity starting materials. We have learned that building quality from the first step saves hours in QC and avoids the stress of unpredictable yields. Over time, we refined our process to reduce side products that had once complicated work-up and crystallization. Careful monitoring of reaction parameters—keeping temperature and pH within narrow bands—shapes a consistent batch every time. This assures a product that gives medicinal chemists and agrochemical formulators a head start, without scrambling to troubleshoot assay results.
This compound has carved out a place in active research labs for a reason. As a halogenated, nitrile-substituted pyridine, it brings two functional handles for cross-coupling and nucleophilic substitution work. That’s more than just chemical jargon—practical utility shows up during scale-up, because many reaction partners tolerate the chloro and nitrile groups without surprise reactivity or degradation. Formulators in the crop sciences reach for this intermediate when building new herbicide scaffolds with desired selectivity. We’ve been told by innovators in the pharmaceutical sector that this molecule opens expressive room for SAR exploration, allowing subtle alterations at the core of the pyridine ring. The result: faster exploration of target activity and fewer headaches during post-reaction purification.
Manufacturing 5-Chloro-3-methylpyridine-2-carbonitrile for regular customers forces us to face scrutiny from analytical teams who trust, but verify. From batch to batch, we follow a consistent specification—color, assay, moisture, and, crucially, impurity profiles. Early on, we saw skeptical eyes when a few ppm of related pyridine byproducts popped in HPLC traces. So we tackled this in two ways. Routine in-process checks at the filtration and crude isolation stages cut the rework needed at the end. Second, we work with both GC and LC methods, not just one favorite approach. Our customers noticed, and their own validation teams now flag far fewer issues—an outcome that grows from direct, daily commitment in the plant.
Getting consistent purity isn’t about chasing impossible numbers. In producing 5-Chloro-3-methylpyridine-2-carbonitrile, we balance tight controls with what matters for end use. Chemists working on structure-activity relationships push for the lowest moisture, and we focus on that by adjusting drying cycles and storage methods. Others want clear data on assay (by area or weight), convinced that anything below 98% purity risks unexpected chromatography or false bioassay signals. After hundreds of production cycles, we take each new requirement as a specific challenge—tweaking work-up, changing drying parameters, or revisiting solvent choices, to keep our product in line with evolving lab needs.
Similar intermediates crowd the catalog, but details matter when performance counts. Compared to 3-chloro or 2-methyl analogs, the structure of 5-Chloro-3-methylpyridine-2-carbonitrile offers predictable selectivity in further functionalization. Locating the chloro group at position 5 and a methyl at position 3 impacts regioselectivity in cross-coupling reactions. We have seen cases where chemists need to build out the nitrile group at position 2, preserving selective reactivity for other sites on the pyridine ring. No guesswork—just clear, repeatable outcomes. This directly saves time during library building, as fewer byproducts mean less time separating target compounds from close relatives.
Another key distinction emerges in solubility and handling. We have tweaked our crystallization and filtration processes, resulting in easier dissolution in common organic solvents compared to certain isomers. End-users noticed fewer clumping or dusting issues during weigh-out. Some pharmaceutical researchers rely on this property when screening at the gram to tens-of-gram scale. In our feedback loop, many synthetic partners told us they can skip preparative HPLC steps by starting with purer, free-flowing material. Each detail, from melting point to hygroscopicity, gets recorded batch by batch. Through years at the bench, we’ve documented that small changes in isomer ratio or residual solvents directly translate into smoother process chemistry—particularly as analytical expectations rise.
Our customers span process chemistry outfits, small biotech startups, leading pharmaceutical developers, and crop protection innovators. Each group has different concerns: for contract research teams, hitting reproducible scaleups is non-negotiable. Pharmaceutical discovery teams count on our rigor in residual solvent testing and impurity reporting. For agrochemical synthesis, predictable reactivity supports rapid optimization of lead compounds. No two projects tap the intermediate in quite the same way, but the through-line is reliability in both performance and documentation. Whether used as a core scaffold or modified in situ, 5-Chloro-3-methylpyridine-2-carbonitrile links molecular design to tangible end products, connecting synthetic ambition with everyday manufacturing discipline.
Every so often, a partner asks, “Can you adapt the form, water content, or packaging?” We log these cases, initiate process trials, and adapt when justified by production data. Not every customization aligns with economic scale, but when a tweak enables a smoother process or higher throughput for a partner, we work towards that. Some years back, we reformulated to minimize static electricity during packaging, reducing sample loss and exposure during transfer. It’s small changes like this that come from being present in the factory, not far removed from laboratory practice. Ultimately, the ability to adjust comes from running reactions ourselves, not sending specs to an unknown subcontractor.
Every chemical manufacturer faces market shifts and regulatory scrutiny. We watch state and international controls for pyridine derivatives and act well ahead of any possible compliance squeeze. Regular site audits, solvent recovery optimization, and cross-checks on downstream traceability keep us ahead of issues that sideline less attentive producers. Analytical standards for 5-Chloro-3-methylpyridine-2-carbonitrile have only tightened over time: routine analysis for residual chlorides, heavy metals, and high-resolution mass spec data is no longer optional. We invest in updating our instrument fleet and standardizing methods, inviting partners and prospective clients to audit and provide feedback. Our records stretch across years and thousands of data points, informing every process improvement or new release batch.
Occasionally, a batch drifts from historic appearance or HPLC purity. Instead of hiding flaws, our process engineers dig into root cause: reactor jacket leaks, unfamiliar trace solvents, or operator error. The solution is rarely found in a manual—it’s about sharing data openly across teams, tracing back to equipment inspection rounds or raw materials documentation. We document outcomes, share lessons on the plant floor, and incorporate every learning, so that the next run delivers clean, reproducible material. Mistakes prompt process review and, if needed, supplier switches or updated cleaning protocols.
We believe that only direct involvement delivers reliability batch after batch in making 5-Chloro-3-methylpyridine-2-carbonitrile. Working in-house means that our engineers and chemists recognize subtle process signals faster than a contract operation using generic equipment. A team familiar with the odors, colors, and quirks of a live batch can flag anomalies in real time. This hands-on oversight means less drift from specification, quicker troubleshooting, and more responsive service to technical queries. In an age where some try to outsource every process and simply compare COAs, maintaining full control over our production unlocks flexibility and stability for customers. Each batch bears the mark of actual effort—from chemists who run the reactions, to operators who track yields and adjust process variables.
Beyond physical product, we field technical questions directly from users who try to adjust parameters in their own work. Each inquiry informs our ongoing technical notes, spanning solvent compatibility, recommended handling procedures, and clean-room storage best practices. These insights grow out of face-to-face problem solving, not scripts or generic advice.
Sustainability pushes us to rethink solvent selection, energy use, and waste management for every synthesis—5-Chloro-3-methylpyridine-2-carbonitrile included. Over several years, process improvements slashed solvent consumption by optimizing phase separations and recycling high-purity streams. Each rework or data-driven downtime led to further savings—less waste, higher yield, improved batch reliability. Packaging has evolved, too. Feedback from partners handling volumes in drummed or bagged formats shaped our switch to antistatic liners and robust, easy-to-open closures.
As each new customer or regulatory update brings fresh requirements, we respond with full transparency about raw material traceability and risk controls. No detail is too small: we document contaminant histories, allergen risks, and shipping conditions to support both internal QC and customer audits. Rather than tweaking COA wording or outsourcing technical queries, we invite customer site visits, share raw data, and compare best practices with open eyes. The result is fewer surprises, not just for our technical team but for every customer working toward their own regulatory or commercial rollout.
The rare intermediates market isn’t static; staying relevant means reading signals from both demand trends and breakthroughs in process chemistry. We monitor shifts in medicinal and agrochemical research and adjust our inventory, production scale, and specification focus accordingly. We face pressure to offer samples on short lead times and bulk shipments that stand up to regulatory review in divergent global markets. With every phone call or technical visit, we learn where synthesis bottlenecks occur and how end-users adapt workflows to changing purity or regulatory standards.
Our experience tells us: real-world success depends on responding quickly to technical hurdles, supply chain snags, or formulation updates. We pool direct plant floor insights, research input, and customer stories to keep 5-Chloro-3-methylpyridine-2-carbonitrile—along with our wider catalog—ready for the next stage of industry evolution. Each change, from specification refinement to investment in automated handling or lab scale process runs, grows from dialogue with those who use what we make. We listen, adapt, and deliver—not from a distance, but from hands-on manufacturing and technical collaboration, every step of the way.
Some of our best process refinements came from open conversations with research clients and production chemists alike. In one instance, a customer found that their downstream coupling reactions gave variable yields across scale. Instead of shifting blame, we sent our process chemist to the client’s site. They examined everything from reagent storage temperatures to water content in the reaction flask. This led us to adjust our own drying curves, invest in new in-line moisture analysis, and tighten our transport and packaging protocols. Results echoed back quickly: the client saw fewer out-of-spec reactions, and we strengthened our process, reducing questions and callbacks.
That experience underscores why operating the plant ourselves—rather than passing off specs—is the key to supporting progressive research. Day-to-day contact between plant operators and synthetic chemists fosters insight. Subtle changes in crystalline form, flow, or dust levels surface in ongoing technical calls, shaping new process steps or changes in equipment setup. These conversations bring practical value, ensuring the product our customers receive supports their work from the gram scale to pilot plant runs.
Global compliance expectations keep tightening for all intermediates, so we stay proactive with both documentation and process validation. From investing in digital batch tracking to routine environmental monitoring, we document every stage of 5-Chloro-3-methylpyridine-2-carbonitrile production. We open our books to customer audits, category-specific queries on genotoxic impurities, and region-specific regulatory updates. This approach builds actual trust. No shortcuts—that’s the difference a real manufacturer can provide, compared to resellers or brokers working with patchy chain-of-custody information.
We treat every technical complaint as a prompt for greater transparency and improvement. For us, full engagement with regulatory changes, open technical feedback, and data-driven process development means every batch of 5-Chloro-3-methylpyridine-2-carbonitrile reflects years of learning and collaboration across the whole value chain.
Every flask, every drum, every lot of 5-Chloro-3-methylpyridine-2-carbonitrile links the reliability of manufacturing to breakthroughs in discovery chemistry. Our team takes pride in growing not only our process capability, but also our technical dialogue with challengers and innovators across the world. At every turn, we prioritize quality, research-driven specification management, and hands-on problem solving. This isn’t just a job—it’s personal, and every batch carries that commitment. Those who work at the bench, develop new actives, and push the boundary in synthesis can see the difference this approach brings, not only in the bottom line but in the tangible results of their own laboratories.