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HS Code |
671951 |
| Chemical Name | 2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile |
| Cas Number | 151666-53-4 |
| Molecular Formula | C8H7ClN2 |
| Molecular Weight | 166.61 |
| Appearance | White to off-white solid |
| Melting Point | 85-89°C |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Smiles | CC1=CC(=NC(=C1Cl)C#N)C |
| Inchi | InChI=1S/C8H7ClN2/c1-5-3-7(2)11-8(9)6(5)4-10 |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 2-CHLORO-4,6-DIMETHYL-3-PYRIDINECARBONITRILE factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White plastic bottle labeled “2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile, 100g,” with hazard symbols, batch number, and manufacturer info. |
| Container Loading (20′ FCL) | 20′ FCL can load 8–10MT of 2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile, packed in 25kg fiber drums or bags. |
| Shipping | 2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile is shipped in tightly sealed containers, protected from moisture, heat, and ignition sources. It is typically transported as a solid, packed according to hazardous material regulations. Proper labeling and documentation are required to ensure safe and compliant delivery. Handle with gloves and personal protective equipment during transport. |
| Storage | **2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile** should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Ensure appropriate labeling and keep out of reach of unauthorized personnel. Use secondary containment to prevent potential spills or leakage. |
| Shelf Life | Shelf life: 2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile remains stable for at least 2 years if stored in a cool, dry place. |
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Purity 98%: 2-CHLORO-4,6-DIMETHYL-3-PYRIDINECARBONITRILE with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity load in final APIs. Melting point 98–101°C: 2-CHLORO-4,6-DIMETHYL-3-PYRIDINECARBONITRILE with a melting point of 98–101°C is employed in agrochemical manufacturing, where it facilitates efficient solid-phase formulations. Molecular weight 180.63 g/mol: 2-CHLORO-4,6-DIMETHYL-3-PYRIDINECARBONITRILE with a molecular weight of 180.63 g/mol is used in fine chemical production, where accurate molar calculations enable precise stoichiometry in multi-step synthesis. Particle size ≤ 50 µm: 2-CHLORO-4,6-DIMETHYL-3-PYRIDINECARBONITRILE with particle size ≤ 50 µm is utilized in catalyst carrier preparations, where fine dispersion leads to uniform catalytic activity. Stability temperature up to 150°C: 2-CHLORO-4,6-DIMETHYL-3-PYRIDINECARBONITRILE stable up to 150°C is used in high-temperature reaction media, where it preserves chemical integrity during process scale-up. |
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From decades of hands-on chemical production, certain intermediates consistently prove their value in real-world laboratory and plant settings. 2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile has become one of those compounds. This molecule—known across the industry for its stable pyridine ring, selective substitution pattern, and straightforward reactivity—serves diverse needs in the synthesis of active pharmaceutical ingredients, crop protection agents, and specialty chemicals. Over the years, we have manufactured this compound to high standards, meeting exacting requirements from end users who depend on reproducibility, scalability, and clean conversion.
Chemists favor this intermediate largely due to its robust structure and selective functionalization. By introducing chlorine, methyl, and nitrile groups at specific positions, this compound strikes a balance between reactivity and stability. In repeated runs and across kilogram to multi-ton production campaigns, we have measured yields and purity levels with consistent outcomes, even as process variables have scaled or shifted. Customers seek this predictability, as uncontrollable batch-to-batch variation disrupts both yield optimization and regulatory documentation.
Working close to the reactors and watching how products behave in real time, certain details gain new significance. 2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile, produced under rigorous protocols, usually appears as an off-white to light-yellow crystalline solid. Analytical runs via HPLC and GC confirm purity levels exceeding 99 percent, typically with trace impurity profiles far below actionable thresholds for downstream reactions. Water content regularly falls under 0.5 percent, removing concerns about hydrolysis or side reactions in sensitive transformations, such as palladium-catalyzed couplings or Grignard additions.
Particle size distribution, often overlooked in laboratory-scale syntheses, becomes critical when producing hundreds of kilograms at a time. After years of practical feedback, our process achieves a consistent distribution that allows uniform feeding into reactors and minimal dusting during handling. We examine each lot for residual solvents, since contamination can sabotage scale-up or downstream processing steps. These factors arise not from a specification sheet, but from decades of feedback from real users—a critical distinction between manufacturing and procurement.
Talk to chemists designing new active compounds, and they often mention the challenge of finding starting points that avoid unnecessary by-products and enable flexible substitution. 2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile offers an efficient entry into various heterocyclic frameworks. The nitrile group, with its electron-withdrawing nature, activates the ring for nucleophilic substitutions at adjacent positions. The chlorine substituent proves invaluable for Suzuki, Buchwald-Hartwig, or other cross-coupling operations, opening access to a broad range of derivatives. Methyl groups at the 4 and 6 positions provide both steric effects and metabolic stability in pharmaceutical and agrochemical molecules.
Pharmaceutical manufacturers seek intermediates that allow for quick generation of candidate libraries, especially for kinase inhibitors, antiviral agents, or neuroactive compounds. Agriscience formulators look for rings protected against photolytic and microbial degradation, which the dimethyl substitutions offer. Fine chemical producers value starting materials that can withstand harsh reaction conditions, as not every downstream synthesis unfolds in gentle laboratory glassware. Over the years, clients relying on our product have cited clean conversion and reduced by-product profiles as their reason for sourcing repeat lots. They rarely ask for unsubstantiated claims—real results on real plants drive return business.
Pyridine derivatives differ widely not just in their location of functional groups, but also in how those changes impact downstream chemistry. For example, 3-chloropyridinecarbonitrile or 2,4,6-trimethylpyridinecarbonitrile each present their own reactivity patterns and limitations. In practice, replacing the 4 and 6 positions with non-methyl groups raises issues of ring instability or decreased solubility. Substituting a nitrile at other positions often leads to unpredictable migration under heating or catalytic conditions.
Through repeated customer dialogues and our own synthetic trials, we've seen the benefit of this specific arrangement—chlorine at the 2-position, methyls at 4 and 6, and a nitrile at 3. Such symmetry delivers a manageable balance: the molecule resists random side reactions yet remains reactive along desired axes. For manufacturers creating diverse libraries of heterocyclic scaffolds, this translates to smoother optimization and fewer surprises during route scouting. Product consistency is not an abstract marketing claim; it happens through relentless process optimization and real troubleshooting when variances do occur.
Manufacturing this intermediate calls for more than simply following a published synthetic route. Scaling a reaction from kilogram to multi-ton batches often unmasks new safety or technical risks—sudden exotherms, unexpected foaming, filtration bottlenecks, or the appearance of trace impurities that disrupt recrystallization stages. At every stage, on-the-ground staff adjust agitation rates, solvent choices, addition protocols, and cooling sequences to head off deviations before they spiral into costly rework or disposal challenges.
Our operators and engineers routinely review historical run data to spot seasonal or supply-related variations. We continually tweak the purification process and implement in-line analytics to catch out-of-spec material before it leaves the plant. In decades of fine chemical manufacturing, we've come to appreciate how early detection of subtle deviations—often invisible on a paper trail—prevents shipping material with hidden liabilities. Every customer feedback round reveals new critical-to-quality attributes, from solubility curves to UV-Vis profiles, reinforcing the reality that specifications alone never tell the full story.
In our facility, packaging and transportation depend on first-hand experience with the physical properties of each product. 2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile, with its moderate melting point and low volatility, avoids many of the headaches common with less stable nitriles. Bulk bags and drums require moisture barrier liners, especially during summer months or when shipping through humid ports. During storage trials, we've observed that temperature excursions above recommended ranges can trigger caking, so we monitor warehouse conditions closely and advise end users on optimal storage practice.
Customers scaling up their own processes often request samples from multiple lots to validate homogeneity and downstream compatibility. We regularly collaborate with technical teams to identify root causes behind incompatibility issues, whether stemming from trace residuals or subtle variations in particle size. The most efficient solutions arise only through transparent exchange of analytical results and production notes between manufacturer and end user. Advice is grounded not in abstract protocols, but in shared trials and the practical lessons learned from every batch, successful or not.
Increasingly, regulators demand transparent sourcing and traceable quality management across the chemical supply chain. Product stewardship is not an option—it builds trust with customers by showing concretely how substandard material never ships out. Each release includes full documentation, with COAs referencing lot-specific analytical data, impurity panels, and process histories. We routinely provide material for registration studies, supplying everything from stability data to impurity stress testing, with raw files sourced from our in-house QC lab. Technical dossiers now contain not just numbers, but a full production narrative to support every regulatory or process audit.
Traceability requires robust documentation, but also direct accountability from staff familiar with both the chemistry and downstream requirements. Inconsistent suppliers often disconnect paperwork from plant realities; years of manufacturing experience bridge that gap by matching theory with on-site practice. End users obtain assurance not just from what we put on a COA but from established relationships and consistent delivery over repeated campaigns. Customers rarely seek the lowest upfront price; more often, production planners and regulatory officers care about upstream process security and a track record of problem-solving.
As pharmaceutical and crop science research expands into new targets, the pressure grows on manufacturers to supply intermediates capable of supporting fast-moving discovery programs. 2-Chloro-4,6-dimethyl-3-pyridinecarbonitrile now supports both patent-protected and generic programs, with real-world applications in kinase inhibitor scaffolds, triazine pesticides, and even materials development. Chemists value predictable behavior under cross-coupling, nucleophilic aromatic substitution, and ring transformation conditions. In our own facility, we observe that process simulations can only go so far before actual plant runs reveal the unique quirks of a new application, driving further refinement in synthesis and purification. The reality of chemical manufacturing lies in inching closer with each cycle to a process that delivers consistently and safely, regardless of the end use.
Recent feedback highlights emerging green chemistry initiatives, pressing for alternatives to hazardous solvents and more efficient atom economy in downstream conversion. Our process engineers collaborate openly with research partners, sharing both successes and failures as we trial alternatives to high-boiling aprotic solvents, recycle wash liquids, and reduce waste during crystallization. Incremental improvements do not draw headlines but they directly affect yield, purity, and environmental footprint at commercial scale. Customers, R&D chemists, and regulatory reviewers all benefit from a candid approach to process optimization, where lessons learned fuel both compliance and safer production.
In any project, realities diverge from textbook expectations. New reactions sometimes throw off unexpected impurities or yield drops, keeping troubleshooting as an everyday part of the job. Our process chemists track both upstream and downstream deviations, logging incidents and sharing root cause analyses with customers. Whether it’s a filter cake collapse or a rare chromatographic tail, open dialogue speeds up corrective action. Over many years, we see that real partnerships—those built on honesty and technical transparency—outperform contracts based solely on price or lead time. Mistakes are inevitable; what matters is how quickly and thoroughly they get resolved.
Peer review groups within the plant discuss run data and brainstorm improvements, often flagging early warning signs before a deviation becomes a production headache. That knowledge base, built through hard-won experience, supports not just our own staff but global teams troubleshooting similar chemistry elsewhere. Each production cycle adds to this shared expertise, reinforcing a culture of learning that ultimately benefits every user in the value chain. Real progress in chemical manufacturing comes in increments, not leaps, with each round of troubleshooting feeding the next cycle of improvement.
Producing chemical intermediates at industrial scale brings safety front and center. Every kilogram of 2-chloro-4,6-dimethyl-3-pyridinecarbonitrile produced must pass not only analytical checks but operator handling trials and HAZOP reviews. Our long-term teams insist on strict compliance not for paperwork’s sake, but because they have witnessed the realities of process upsets and accidental exposures. Fume extraction, PPE, and incident drills are daily routines, not regulatory requirements on paper. Manufacturing for global pharma and agro markets raises the bar; we audit every stage ourselves and never rely solely on supplier certificates or external findings.
Sustainability drives daily decisions. We track not just solvent use and waste generation, but process emissions and energy consumption. Substituting greener solvent systems or implementing closed-loop water cooling brings tangible benefits inside the plant, as physical working conditions improve and regulatory risk falls. Switches to renewable energy, landfill diversion, and by-product valorization take years to implement but reflect concrete improvement in real-time environmental impact. Partnering with downstream users, we routinely exchange ideas for further minimizing the environmental footprint, delivering results that regulatory teams recognize as grounded in day-to-day manufacturing rather than abstract sustainability vision statements.
Decades in pyridine derivative manufacturing reinforce a simple truth—the chemistry is only half the story. Customers return not for a molecule in isolation, but for a reliable supply chain, technical backup, and an open channel to seasoned process chemists. Each new project exposes alternative pathways, new micro-impurities, or unanticipated regulatory requirements. The advantage comes not from rigid adherence to static protocols, but from flexibility, transparency, and a commitment to honest reporting of both successes and failures. As industry requirements grow ever more complex, the interplay between technical experience and field reality determines which manufacturers remain true partners over time.
Whether shipping to major pharmaceutical synthesis plants, crop protection formulators, or advanced material startups, we invest in the relationships that keep products fit for modern needs. Future directions will increasingly demand tighter impurity control, safer manufacturing conditions, and lower environmental impact. Our experience manufacturing 2-chloro-4,6-dimethyl-3-pyridinecarbonitrile grounds us in the reality that progress, while sometimes incremental, delivers reliability batch after batch—and trust, built over long-term collaboration, brings real value to all involved in the supply chain.