|
HS Code |
854334 |
| Cas Number | 178590-48-6 |
| Molecular Formula | C6H5Cl2N |
| Molecular Weight | 162.02 |
| Iupac Name | 2,3-dichloro-4-methylpyridine |
| Pubchem Cid | 12020595 |
As an accredited Pyridine, 2,3-dichloro-4-methyl- (9CI) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of Pyridine, 2,3-dichloro-4-methyl- (9CI), tightly sealed with a screw cap, labeled with hazard warnings. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for Pyridine, 2,3-dichloro-4-methyl- (9CI): 12-16 metric tons packed in UN-approved drums. |
| Shipping | Pyridine, 2,3-dichloro-4-methyl- (9CI) should be shipped in tightly sealed containers, stored in a cool, dry, and well-ventilated area. It is classified as a hazardous chemical and should be transported according to relevant regulations, ensuring proper labeling and documentation, with measures to avoid spills, leaks, or exposure during transit. |
| Storage | Pyridine, 2,3-dichloro-4-methyl- (9CI) should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Store at room temperature and away from ignition sources, as it is flammable. Use appropriate containment to minimize environmental release and follow safety guidelines. |
| Shelf Life | Shelf life of Pyridine, 2,3-dichloro-4-methyl- (9CI): Typically stable for 2-3 years when stored in cool, dry conditions. |
|
Purity 98%: Pyridine, 2,3-dichloro-4-methyl- (9CI) with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high product yield and reduced impurity profiles. Melting Point 45°C: Pyridine, 2,3-dichloro-4-methyl- (9CI) with a melting point of 45°C is used in agrochemical formulation processes, where well-defined phase transitions improve processing efficiency. Molecular Weight 178.02 g/mol: Pyridine, 2,3-dichloro-4-methyl- (9CI) with a molecular weight of 178.02 g/mol is used in heterocyclic compound libraries for research, where precise molecular mass enables accurate analytical characterization. Stability Temperature 60°C: Pyridine, 2,3-dichloro-4-methyl- (9CI) with stability up to 60°C is used in industrial manufacturing, where thermal stability maintains compound integrity during high-temperature reactions. Particle Size < 50 µm: Pyridine, 2,3-dichloro-4-methyl- (9CI) with particle size below 50 µm is used in catalyst carrier production, where fine granulometry enhances dispersion and reaction kinetics. Water Content < 0.5%: Pyridine, 2,3-dichloro-4-methyl- (9CI) with water content below 0.5% is used in anhydrous synthesis environments, where low moisture content reduces side reactions. |
Competitive Pyridine, 2,3-dichloro-4-methyl- (9CI) prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
Chemistry drives practical results when attention to quality carries through every batch. Pyridine, 2,3-dichloro-4-methyl- (9CI) did not start as a familiar name across the fine chemicals sector. Over decades of production and hands-on troubleshooting, we have learned how its particular profile sets it apart and opens up a surprising range of possibilities. Here, from the reactor floor and quality control desk alike, you will find details that matter to anyone depending on this compound.
2,3-dichloro-4-methylpyridine draws out its unique features straight from its chemical backbone. Pyridine rings by nature provide reactivity and solubility that tick off core needs in specialty synthesis and intermediate production. Chlorination at the 2 and 3 positions, coupled with a methyl group at the 4-position, changes not just the reactivity, but stability, storage profile, and downstream compatibility.
From the manufacturing viewpoint, tracking these modifications delivers more than molecular theory. The dual chlorination blocks unwanted side reactions for those demanding processes where purity fluctuations can gum up high-value runs or trigger compliance headaches. A methyl group stabilizes the electron cloud, shifting the compound’s behaviour under real-world conditions in contrast to unsubstituted or mono-chlorinated alternatives.
This background sets the stage for its adoption across our customer base—from pharmaceutical intermediates to crop protection R&D, pigments and beyond.
The breadth of applications does not relieve pressure on the details. Day in and day out, we target a purity benchmark that reflects the needs of regulated end-users. Typical output leaves the plant above 98% purity by GC, and in practice, routine testing weeds out batch-to-batch inconsistencies, not just based on numbers, but on how those variations actually affect downstream yields and reproducibility.
Not every customer’s process will react kindly to hints of isomer contamination, colored residues, or extraneous moisture. As a manufacturer, we monitor not only standard contaminants, but also minute variations in trace by-products originating from halogen-source quality shifts, slight temperature deviations during the ring chlorination step, and the residence time of feedstocks in our reactors. Customers have come to expect a tightly defined melting point ridge, low residue on evaporation, and clean spectral signatures—the baseline for those running sensitive transformations.
Plastic or glass packaging might suit small lab use, but drums designed for industrial handling keep moisture pick-up, shock, and thermal swings in check. We pressure-test new package suppliers under our warehouse climate conditions, knowing full well a leaky liner or subpar closure can write off thousands of dollars in high-value intermediates. It is not enough for the product to ship out pure; it must arrive in the same state, with all physical and chemical properties intact.
Every season brings a new challenge as formulators and synthetic chemists stretch production processes or regulatory standards shift. Pyridine, 2,3-dichloro-4-methyl- (9CI) finds its place as an intermediate in innovative pharmaceutical campaigns, specifically those complicated by aromatic halogen exchange, N-alkylation, or coupling protocols. Where the market leans on advanced herbicides, the molecule fits as a scaffold for selective chlorination, forming the backbone in the search for more environmentally considerate actives.
Dye and pigment manufacturers see value in the compound's balance between reactivity and resistance to secondary hydrolysis, making it a candidate for high-performance, long-wear systems. In agricultural chemistry, it offers a starting point for molecules requiring tight control over electron-donating and -withdrawing groups, letting formulators tune bioactivity without opening the door to unwanted by-products.
Our plant engineers field inquiries nearly every quarter from customers attempting to replace earlier-generation pyridines or chlorinated aromatics. They want the selective reactivity without the tail of persistent by-product or off-coloration issues that occasionally appeared with more generic feedstocks. Many process engineers still remember headaches caused by other dihalopyridines, such as fusion-step fouling, or disposal headaches from high organic halide content. The 2,3-dichloro-4-methyl variety strips out complications by virtue of its structure—less loss to recovery, less trouble in final purification, and cleaner compliance paperwork.
Contrasts with mono-chloro, 2,4-dichloro, or non-methylated analogues show up in both practical and financial terms for a plant engineer or chemist. Single-chlorine substitutions often yield broader product slates during cross-coupling. Di-chlorination at the 2 and 3 positions closes off unwanted reactivity on those sites, reducing formation of tars or resinous by-products. Adding the methyl at position four pushes the compound further down the road toward flexibility: with fewer polar sites, it resists solvents that might strip away more ordinary pyridines.
Highly experienced formulators tell us that switching from 2-chloropyridines or simpler heterocycles sometimes cuts final yields when those alternatives introduce extra reactivity at troublesome positions. These differences become most apparent under scale-up or regulatory scrutiny.
Our lab has fielded dozens of customer inquires where users struggled with unwanted side reactions from competitors’ 2,4-dichloro products. Such products, born from a different halogenation approach, tend to allow unexpected addition or elimination reactions, especially when exposed to nucleophilic media. In contrast, the 2,3-dichloro-4-methyl configuration offers more predictable outcomes, particularly in routes involving alkylation, where methyl stabilization maintains consistency batch after batch.
Facilities handling brighter dyes or agrochemicals value this level of control, and their feedback shapes our day-to-day focus. In those markets, off-reactivity and material loss press against profit margins, and only the steadfast stability and fine-tuned chlorine substitution profile of this compound rises to the challenge.
Not everything runs smooth, even with a carefully tuned process. Over years, equipment upgrades and process optimization have left a mark on what we consider standard production. Years ago, minor impurities or deviations in final product color used to cost us precious time and money on reprocessing or raw material reclamation. Sensors and control systems only do so much. Real-world improvements came from practical knowledge—operator training, feedback from downstream plants, and relentless batch data comparisons.
QC feedback from customers initiated many of our purity and packaging changes. One manufacturer of active intermediates flagged a spike in side-reaction waste not visible in the standard certificate of analysis. They traced it to trace isomers that emerged only during a particular sequence at elevated temperature. Our lab matched the anomaly after three weeks of small-scale recreation, leading to a revision in precursor selection. These are not textbook issues; they are the daily grind of chemical manufacturing.
We measure packaging loss at each step and frequently run stress tests in transport. Extra moisture or plasticizer extraction from barrels might not show up for weeks, but these early failures will turn up as batch inconsistencies at our customers’ plants months later. This vigilance has become a core part of delivering a product with both the precision and reliability demanded in these high-value applications.
Production experience sets the tone for how we approach downstream safety. Pyridine, 2,3-dichloro-4-methyl- (9CI), like most halogenated pyridines, needs careful treatment. Avoiding direct skin contact or vapor exposure is critical, and local exhaust ventilation remains the industry’s best tool for maintaining safe working conditions during handling or transfer. Environmental standards push us to reclaim as much material as possible—not simply for cost, but to reduce risks for workers and the wider community.
Years of tracking regulatory scrutiny highlights the importance of honest, data-backed transparency. From REACH dossiers to GHS labeling, everything boils down to showing not only that the product meets specs, but that its life cycle, right down to the drums, withstands outside review.
Sustainability pressures do not stop at regulatory paperwork. We work on continuous improvement projects, trialing alternative recycling and purification setups, with an eye toward both efficiency and long-term community safety.
Some compounds gather dust as commodity building blocks; others earn a reputation as problem-solvers. We field inquiries from chemists who run the gamut: some looking for highly specific impurity profiles, others in need of robust, no-nonsense intermediates for scaling up from pilot to commercial scale. Pyridine, 2,3-dichloro-4-methyl- (9CI) earns repeat business in both camps.
Industrial crop science teams report on its ease of purification in scale-up, leading to cleaner residues in the end product, and thus less trouble flipping between product grades for different export markets. Pharmaceutical formulators emphasize the time savings when batch-to-batch reactivity remains stable, especially during late-stage intermediates where a deviation can result in months of lost time and retesting.
We glean insights every quarter through technical support requests: how the material copes with sudden step changes in process temperature, which ancillary solvents lead to unexpected discolorations, or what small tweaks in storage conditions prevent product drift. These issues all filter back to production, tightening our batch review process each time.
The backbone of steady production does not mean change stops. Ongoing campaigns with supply chain teams foster improved packaging, better response to seasonal shifts in raw material quality, and backup plans for transportation bottlenecks. Investment in advanced GC-MS and elemental analysis equipment allows us to profile each step of production for trace-level contaminants, nailing down the root of any observed outlier.
Employee retention matters. Long-term staff know our equipment quirks and toll processing routines inside out. Their experience forms a bridge between what is possible in the lab, and what is achievable at the ton scale, and this drives process tweaks that incrementally tighten our output year after year.
Certifications and audits keep us on our toes, but real trust comes from customers who run the product through their own systems and get predictable, clean results. Every technical support case loops back into standard operating updates, reinforcing a cycle of reliability.
No industry stands still, and every major market—especially pharmaceuticals and agrochemicals—brings regular shifts in compliance, sustainability targets, or global supply chain turbulence. These shifting demands mean that a product made with last year’s tolerances, or stored in outdated packaging, exposes both customers and producers to risk.
Staying ahead means investing not only in production technology but also in detailed market knowledge. Early warning signs flag up through direct conversations with downstream users and a readiness to modify raw material sources when tighter environmental regulations land. For example, several herbicide manufacturers now expect third-party verified evidence of trace halide content, pushing us to retool parts of the purification process.
Production teams remain vigilant for new waste management strategies compliant with both local and international guidelines. Spent solvents and residues from the pyridine process receive detailed tracking and documented solvent reclamation, meeting new eco-profile demands without breaking production efficiency.
The chemical manufacturing landscape brings logistical and technical hurdles at every stage. But over time a flexible, firsthand understanding of both the molecule and its market context turns into reliability that downstream users can trust. Our approach to Pyridine, 2,3-dichloro-4-methyl- (9CI) is not about generic intermediates but targeted application—backed by batch consistency, responsiveness to technical feedback, and a track record of successful real-world deployment.
From our perspective, this is what makes a high-value intermediate: not just a compound with two chlorines and a methyl on a pyridine ring, but a consistent, predictable workhorse in the hands of those building tomorrow’s molecules. Every batch tells a story, built on decades of hands-on problem-solving and continuous refinement.