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HS Code |
684982 |
| Cas Number | 19749-50-3 |
| Iupac Name | 2-chloro-4-methylpyridine-3-carbonitrile |
| Molecular Formula | C7H5ClN2 |
| Molecular Weight | 152.58 g/mol |
| Appearance | White to pale yellow solid |
| Melting Point | 49-52°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Smiles | CC1=CC(=C(N=C1)Cl)C#N |
| Inchi | InChI=1S/C7H5ClN2/c1-5-2-6(4-9)7(8)10-3-5/h2-3H,1H3 |
| Synonyms | 2-Chloro-4-methyl-3-cyanopyridine |
| Storage Conditions | Store in a cool, dry place, keep container tightly closed |
As an accredited 3-Pyridinecarbonitrile, 2-chloro-4-methyl- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g amber glass bottle labeled "3-Pyridinecarbonitrile, 2-chloro-4-methyl-" with hazard warnings, CAS No., and supplier information. |
| Container Loading (20′ FCL) | 20′ FCL container loads 160-180 drums (25kg each) of 3-Pyridinecarbonitrile, 2-chloro-4-methyl-, totaling 4-4.5 metric tons. |
| Shipping | **Shipping Description:** 3-Pyridinecarbonitrile, 2-chloro-4-methyl- is shipped in tightly sealed containers, compliant with chemical transport regulations. Protect from moisture, incompatible materials, and physical damage. Label with appropriate hazard warnings. During transit, keep away from heat and direct sunlight. Ensure compliance with DOT, IATA, and IMDG standards for chemical shipments. |
| Storage | 3-Pyridinecarbonitrile, 2-chloro-4-methyl- should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers. Protect from moisture and direct sunlight. Keep the chemical in a designated chemical storage cabinet, and ensure proper labeling. Use secondary containment to prevent leaks or spills and limit access to authorized personnel only. |
| Shelf Life | Shelf life for 3-Pyridinecarbonitrile, 2-chloro-4-methyl- is typically 2–3 years when stored tightly sealed in a cool, dry place. |
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Purity 99%: 3-Pyridinecarbonitrile, 2-chloro-4-methyl- with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield of target active ingredients. Melting Point 96°C: 3-Pyridinecarbonitrile, 2-chloro-4-methyl- with melting point 96°C is used in fine chemical formulation, where it enables temperature-controlled processing. Particle Size <50 μm: 3-Pyridinecarbonitrile, 2-chloro-4-methyl- with particle size less than 50 μm is used in catalyst preparation, where it ensures uniform dispersion and reactivity. Stability Temperature 150°C: 3-Pyridinecarbonitrile, 2-chloro-4-methyl- with stability temperature of 150°C is used in high-temperature organic reactions, where it maintains structural integrity and reactivity. Assay ≥98%: 3-Pyridinecarbonitrile, 2-chloro-4-methyl- with assay ≥98% is used in agrochemical production, where it provides consistent formulation quality. Water Content ≤0.5%: 3-Pyridinecarbonitrile, 2-chloro-4-methyl- with water content ≤0.5% is used in electronic chemical manufacturing, where it minimizes unwanted side reactions. |
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Working on the synthesis and production line for fine chemicals, you know the difference real-world experience brings. We have dedicated a lot of effort to mastering 3-pyridinecarbonitrile, 2-chloro-4-methyl-. You may see plenty of datasheets on the web, but the real story behind a molecule sits in how it’s made, how it performs in a lab or industrial reactor, and what sort of value it brings to busy project teams. Years of handling this molecule in bulk and lab scale, running the columns, adjusting the heat slowly to keep yields high—these give a kind of insight the spec sheet never does. Subtle operational tweaks, supply sourcing, dealing with energetic intermediates—it all leads to a compound that tracks cleanly for downstream needs in pharma, specialty intermediates, and fine chemical research.
You run across a lot of pyridinecarboxylic acid derivatives over time. The 2-chloro-4-methyl substituted version, also recognized by its CAS number 113306-86-8, stands apart. Its structural substitution gives it a unique balance: the chloro group at the 2-position brings certain reactivity, especially in terms of the electron withdrawing effects, while the 4-methyl tilts solubility slightly higher compared to non-methylated analogues. We’ve compared this molecule against other pyridinecarbonitriles on the bench—one of the first things you see is easier handling, lower hygroscopicity, and a more predictable melting behavior under repeat production campaigns.
Over the years, we’ve scaled from pilot labs producing a few kilos at a time to multi-ton runs. Each campaign, our team measures not only for purity (which typically runs 99%+ by HPLC, and always above 98%) but also for reproducibility. Process tweaks over time—solvent choice, controlled addition rates, careful monitoring of temperature windows—have helped us keep batches uniform. Colleagues in downstream synthesis appreciate not chasing side products or odd tints in NMR spectra. In our trials, the typical lot forms a white to pale yellow solid with a melting point in the expected 70–75 °C range. Subtle impurities fall below detection by GC-MS in most analytical runs.
Most of the volumes go into pharmaceutical intermediates—either as a building block in the synthesis of advanced heterocyclic scaffolds, or for creating API intermediates where the pyridine ring plays a role in binding, navigation, or metabolism. In commercial projects, we’ve seen clients use it to craft kinase inhibitors and antimicrobial leads, where the ortho-chloro group assists in later cyclizations or amidation steps. On the production side, those using the molecule give positive notes for its solubility in common organic solvents—DMF, acetonitrile, and DMSO—and how cleanly it transfers through filtration and separation steps. Nobody wants a sticky cake at the filter, and this molecule tends to come out as a dry, manageable mass.
Some years ago, a major client switched from a 3-chloropyridinecarbonitrile to this 2-chloro-4-methyl variant. The reason, echoed by many others, can be traced to application outcomes. Reactions, especially for nucleophilic aromatic substitution, run smoother. There are fewer issues with unwanted side reactions at the pyridine nitrogen, and the methyl group at the 4-position shields the ring against over-oxidation or unexpected reactivity. Technicians tell us this simplifies process optimization downstream, slashing time needed for column or prep workups. In some applications requiring biaryl coupling or Suzuki reactions, we’ve found yields jump when using this specific compound, as compared with unsubstituted or 3-chloro variants.
There’s a marked difference in storage, too. Some analogues draw moisture like magnets and clump in standard containers, but 3-pyridinecarbonitrile, 2-chloro-4-methyl- remains stable under lab conditions. Larger clients appreciate not needing elaborate dry-room setups just to keep the product usable. Our team works to guarantee stability for at least two years in sealed, PE-lined drums placed in standard ambient conditions, without significant darkening or caking.
This molecule isn’t always simple to source in high volumes—don’t let casual supplier lists online fool you. Availability depends on reliable access to high-purity 2-chloro-4-methylpyridine precursors. Over the past decade, we’ve invested in long-term relationships with upstream syntheses. Chlorination steps require close control to avoid over-chlorination, and controlled conditions for the cyanation keep byproducts to a minimum. Without solid process R&D, impurity profiles can become tricky; our own engineers spent a year developing a purification flow that scrubs residual chloropyridinium salts and trace halide residues. These details may sound operational, but they radically affect how pharmaceutical clients approach qualification.
Shipping and handling also deserve mention. Many fine chemicals in this class have hazardous shipping codes, particularly due to potential toxicity. We train logistics teams to observe UN recommendations and use leak-proof primary containers. Real-life events taught us that simple double-bagging and drum line inserts beat “just-in-time” bulk bags, which can develop micro-leaks or absorb moisture over weeks in transit. Every drum we send out has been studied for closure integrity—a lesson we learned from years troubleshooting client complaints that ranged from sticky residues to vapor pressure build-up in hot summers.
These days, the regulatory focus is intense. We monitor purity and residual solvents not only for process efficiency but also to meet rigorous limits stemming from REACH, TSCA, and local environmental guidelines. Volumes over a certain threshold require notification under REACH; full QSAR and documented impurity profiles become essential for finished drugs, especially in the EU. Our team led a multi-year study, working with outside analytical chemists, to clear all relevant heavy metal and residue benchmarks. Solvent waste from the process is recovered and recycled. Across the past five years, we have worked steadily to move from chlorinated extraction solvents—now using ethanol, where possible—and run a train of low VOC capture for any vent streams.
Waste handling cannot be left as an afterthought. Ethically and legally, we handle waste in sealed, licensed drum systems. We process all chlorinated waste streams at certified treatment centers rather than venting or on-site burning. The point: clients need assurance the products they receive don’t carry hidden environmental headaches that may crop up later. We have adopted online solvent tracking for the full chain, from precursor to drum, to offer full traceability for audits or customer inquiries.
In contract manufacturing, project managers demand batch histories and sample retention logs. Every kilogram is mapped to a unique batch code with documented chain-of-custody files. Over roughly 700+ lots shipped across a decade, we have almost never faced a recalled shipment. On the ground, our warehouse keeps two year’s worth of samples, stored at ambient temperature. These serve in root-cause investigations, regulatory inspections, and customer qualification runs. Each batch ships with a tailored certificate of analysis (CoA) covering not just content, but NMR, HPLC, and GC-MS proof, plus a water content determination (typically under 0.1%).
What’s often overlooked: documentation isn’t just paper generated for compliance. Clients in pharma or advanced materials run pilot studies and need older samples for requalification, so we keep them organized and ready to send out within 24 hours. Personal experience managing sample logistics reinforces the value—there is nothing more frustrating than chasing a lost or forgotten sample after a project flag is raised.
Direct users in process chemistry and medicinal R&D rely on speed and lack of headaches during scale-up. A top ten pharma company conducting combinatorial synthesis on pyridines switched to our material after screening four other sources. Their feedback: conversions improved, downstream reactions cleaned up, and technical support made a difference. The core structure of 3-pyridinecarbonitrile, 2-chloro-4-methyl- enables fewer steps to reach complex building blocks, providing synthetic access to highly substituted heterocycles. Contract manufacturing organizations (CMOs) rely on short lead times and replacement lots that behave just like previous shipments. We have invested in robust inventory and flexible production scheduling. One of the biggest advantages for customers is the on-site technical support—if purification or solubility issues occur, labs can quickly troubleshoot issues alongside the manufacturing chemists responsible for each lot.
Not only pharmaceuticals make use of this molecule. We have shipped drums to agrochemical formulators looking for a stable, halo-substituted pyridine to plug into new insecticide and fungicide scaffolds. Material science labs apply it in surface modification studies, leveraging its physical robustness and clean behavior in coupling reactions, especially on modified glass surfaces and polymers. It’s a favorite for exploratory chemistry because it stays consistent in reactions where other heteroaromatic nitriles throw off ambiguous byproducts.
After years of shipping to clients on five continents, we track the molecule’s stability in diverse climates—humid tropics, cold northern zones, and everything in between. Early on, we saw caking and color changes on the longest logistics routes, usually due to substandard packaging or warehouse conditions. We moved exclusively to sealed, double-lined PE drums. End user stories confirmed improvement: less caking, fewer darkened samples, and more consistent weighing in high-throughput labs. In our internal stability studies, typical product in these packages holds purity above 98% for at least 24 months at 25 °C, even in environments with summer humidity over 80%. That reduces scrap and requalification headaches for everyone.
Technologists and process engineers frequently compare our product directly with similar nitriles, often noting fewer filtration difficulties and a lower tendency to form stubborn emulsions during work-up. We have spent years refining parameters for isolation and drying, learning from pilot batches that left crystalline residues or gummy residues. Now, the final step brings clean, dry material that flows freely. Improved isolation has also lowered residual solvent content to levels well within international standards. That makes the material friendlier to both equipment and operators.
Trends shift in specialty chemicals. What’s needed in 2024 is not what was needed a decade ago. Sourcing reliability stands at the top—most end-users cannot afford downtime due to weak supply chains. The pandemic underscored this point: supply disruptions upended projects across the globe. As actual manufacturers, we control the whole production stream. That gives us leeway to make fast adjustments and ensure delivery windows that some third-party traders can’t guarantee. Investment in raw materials inventory and just-in-case capacity helps immunize our partners from stockouts.
Scaling up always brings hidden risks. At each volume milestone, unexpected equipment fouling, waste loads, and worker safety concerns emerge. Our plant operates with enhanced ventilation and scrubbing, and regular hands-on training keeps the workforce ready for process upsets. The downstream chemical industry leans heavily on upfront transparency to sort these issues. Direct communication between process chemists, plant operators, and client technical teams cuts ramp-up time and limits surprise solvent issues or raw material impurities.
Clients occasionally ask how to push this product further—perhaps for new cross-coupling experiments or as part of new high-throughput screens. We work closely alongside researchers, running bench tests in parallel, and help adjust crystallization to maximize throughput. This kind of support grows out of years on the floor, adapting quickly when clients submit new use cases or raise questions spotted only by experienced bench chemists.
The real value to industrial users goes beyond purity or price. We have forged ongoing partnerships with clients by providing comparative GC-MS traces on request, rapid troubleshooting, and access to the actual chemists who made the last batch. Questions that land on our desks range from stability in specific solvents, optimum storage suggestions, to batch-to-batch trace metal tracking. We can answer efficiently because the knowledge stems from the actual production and analytical records, not just a marketing or third-party perspective.
If you work day after day with specialty chemicals, what matters most is reliability, process transparency, and a consistent product backed by real experience. Our story of producing 3-pyridinecarbonitrile, 2-chloro-4-methyl- is one of continuous process improvement, open communication with technical users, and attention to details that only hands-on manufacturing affords. Our aim remains to support innovative chemists—whether the goal is a new API, an advanced agrochemical, or a novel material—by delivering every lot with the same confidence born of seeing the process through from precursor selection to final shipment.