|
HS Code |
258561 |
| Chemical Name | 2,5-dichloro-3-pyridinecarboxylic acid |
| Cas Number | 24527-66-8 |
| Molecular Formula | C6H3Cl2NO2 |
| Molecular Weight | 192.00 g/mol |
| Appearance | White to pale yellow solid |
| Melting Point | 220-224°C |
| Solubility In Water | Slightly soluble |
| Purity | Typically >98% |
| Storage Conditions | Store in a cool, dry place, tightly closed |
As an accredited 2,5-dichloro-3-pyridinecarboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100-gram amber glass bottle, tightly sealed, labeled "2,5-dichloro-3-pyridinecarboxylic acid," with hazard warnings and batch information. |
| Container Loading (20′ FCL) | 20′ FCL container typically loads 12-14 metric tons of 2,5-dichloro-3-pyridinecarboxylic acid, packed in 25 kg fiber drums. |
| Shipping | 2,5-Dichloro-3-pyridinecarboxylic acid is shipped in tightly sealed containers, protected from moisture and light. The packaging complies with relevant chemical transport regulations, ensuring safe handling and transit. Proper labeling and documentation are provided. During shipping, the material is kept in a cool, dry environment to prevent decomposition and contamination. |
| Storage | 2,5-Dichloro-3-pyridinecarboxylic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Protect it from moisture and direct sunlight. Ensure the storage area is clearly labeled, and follow appropriate chemical hygiene practices. Avoid contact with skin and use proper personal protective equipment when handling. |
| Shelf Life | 2,5-Dichloro-3-pyridinecarboxylic acid is stable under recommended storage conditions; typically, its shelf life exceeds two years. |
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Purity 98%: 2,5-dichloro-3-pyridinecarboxylic acid with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high reaction efficiency and product consistency. Melting point 170°C: 2,5-dichloro-3-pyridinecarboxylic acid with a melting point of 170°C is used in fine chemical manufacturing, where it provides stable thermal processing conditions. Particle size <50 µm: 2,5-dichloro-3-pyridinecarboxylic acid with particle size below 50 µm is used in agrochemical formulation, where it improves dispersion and uniformity in the final product. Molecular weight 208.02 g/mol: 2,5-dichloro-3-pyridinecarboxylic acid with a molecular weight of 208.02 g/mol is used in catalyst development, where it enables precise stoichiometric calculations and reproducibility. Stability temperature up to 120°C: 2,5-dichloro-3-pyridinecarboxylic acid with stability up to 120°C is used in polymer additive applications, where it maintains compound integrity during processing. Water content <0.5%: 2,5-dichloro-3-pyridinecarboxylic acid with water content less than 0.5% is used in electronic chemical manufacturing, where it minimizes the risk of hydrolytic degradation and enhances product reliability. Chlorine content 34%: 2,5-dichloro-3-pyridinecarboxylic acid with chlorine content of 34% is used in pesticide synthesis, where it contributes to effective halogenation and target-specific activity. Assay (HPLC) >99%: 2,5-dichloro-3-pyridinecarboxylic acid with HPLC assay above 99% is used in research scale compound synthesis, where it guarantees high purity and minimizes impurity interference. Residual solvent <100 ppm: 2,5-dichloro-3-pyridinecarboxylic acid with residual solvent below 100 ppm is used in medical device material production, where it assures product safety and regulatory compliance. |
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At our manufacturing site, 2,5-dichloro-3-pyridinecarboxylic acid remains a benchmark product that reflects real experience and laboratory precision. Day in and day out, our staff witness how nuanced changes in reaction conditions influence purity, yield, and handling. The hands-on nature of our work means every lot heading out the gate gets the same level of scrutiny as the very first batch we ever produced. Each application from end users leaves a footprint, guiding improvements in how we approach both production and quality management. This commentary shares what we have learned about this material, both on the production floor and in the field.
This compound’s structure features a pyridine ring with two chlorine atoms at the 2 and 5 positions, along with a carboxylic acid group anchoring the 3 position. The chemical formula C6H3Cl2NO2 and molecular weight of 192.00 define its core, but the actual physical properties are shaped by production subtleties. Our current primary product appears in the form of an off-white to pale yellow crystalline powder. Most labs receive it at a minimum purity of 98%, proven batch after batch by HPLC and NMR analysis. Moisture content stays below 0.5% when properly handled. Impurities, especially those involving residual solvents or di- and mono-substituted byproducts, hold the tightest limitations. Our experience shows that even a stray halide or unreacted starting material can throw off later-stage chemistry or cause headaches downstream, so our process design targets exceptional control.
From a packaging angle, we have found that double-bagging inside high-density polyethylene drums works best to limit both moisture ingress and static dusting. Even at scale, handling characteristics stay predictable: the material does not clump or cake under ambient storage, and it exhibits a crisp flow, crucial when feeding automated dosing systems in large synthesis operations.
Synthesizing this acid poses challenges and rewards for any manufacturing chemist. Over the years, we have run countless campaigns with pressure reactors and open atmospheric systems. The heart of the route relies on careful chlorination steps followed by controlled hydrolysis. Managing reaction heat transfers and gas purging is essential to avoid over-chlorination or forming naphthyridine impurities, which tend to sneak in if controls slip. Our plant operators monitor color, temperature, and gas flow meter readings constantly for this reason.
On a bad day, runaway chlorination plumes can force full system shutdown and weeks of reactor cleanout. On a good day, tight phase separation and temperature control pay off in a clean, high-yielding crystallization. Every batch tells us more about how subtle changes shape the final product, so our team tracks data on every parameter: agitator speed, solvent ratios, chlorination rate, and much more. This data pool now guides production scheduling and campaign planning to maximize output and limit interruptions.
The main commercial draw of 2,5-dichloro-3-pyridinecarboxylic acid comes from its dual identity—it serves both as an intermediate and as a building block with direct use. On the synthesis side, agrochemical makers frequently rely on its structure to create fungicides, herbicides, and growth regulators. Our technical staff often fields requests for high-purity lots destined for large multinational herbicide producers, who value tight impurity profiles to protect their actives from unwanted side reactions. The rigid purity criteria, set by these formulators, has reshaped how we approach analytics and release protocols in our plant. Simple spot testing never suffices; we routinely generate full chromatographic fingerprints for each delivery.
Pharmaceutical makers show similar interest, especially those synthesizing anti-inflammatory or anti-viral agents. Use cases extend from coupling chemistry—where the carboxylic group links with diverse amines or alcohols—to installations of other functional groups on the active halide positions. The pyridine ring’s inherent reactivity offers versatility for researchers exploring novel compounds, and having a stock of reliable, consistent acid speeds up their timelines. Over time, our work with biotech pilot plants has seen this compound used for everything from process development studies to regulatory submission batches.
Outside agriculture and pharma, some polymer and electronics firms source this acid for custom catalyst development, colorant manufacture, and, in rare cases, as a component in liquid crystal research. End-users in these sectors tell us that trace-level impurities can easily disrupt their processes, so we collaborate closely on custom purification runs. Advanced filtration and recrystallization protocols—based on lessons from hundreds of campaigns—now underpin our approach to their projects.
Growth in modern herbicide and pharmaceutical markets has forced us to strengthen both output and consistency. Our manufacturing schedules no longer follow strict batch-by-batch procedures. Multi-ton demand cycles have triggered major changes, including a shift toward semi-continuous and modular operations. We upgraded process automation with distributed control systems, allowing faster tweaks in pressure and reagent dosing, reducing human error, and increasing reproducibility. Meanwhile, we don’t ignore the small custom lots: research groups, from university spinouts to contract labs, still look to us for specialized production and troubleshooting know-how.
This evolving landscape affects supply chain practices at the raw materials side, too. A single missed delivery of key chlorinating agents can set production back for weeks, so our procurement team cultivates direct links with upstream chlor-alkali manufacturers. Each contract factors lead times, solvent purity standards, and even seasonal fluctuation in logistics. Our experience suggests that real system robustness emerges from this integrated supply mentality—not from overreliance on spot markets or generic stocks.
Many customers come to us after previously working with other halogenated pyridinecarboxylic acids, such as the 2,6- or 3,5-dichloro analogs. Over the years, side-by-side trials prove that the positional isomerism drives not just reactivity but also stability and downstream compatibility. For instance, the 2,5-dichloro variant’s spatial configuration provides a unique signature for electrophilic substitution. We have seen cases where formulators initially use the 2,6-isomer, only to switch after solubility or coupling reactions falter. Our feedback from contract manufacturers regularly points to the 2,5-pattern offering cleaner product isolation, with less side-reaction tarring than other isomers.
In our own scale-up projects, the 2,5-dichloro material consistently yields higher overall reaction rates in multi-step synthesis than mono-chloro or non-halogenated benzoic acids. The symmetric halogenation profile often translates to sharper melting points and better controlled crystallization. In practice, this means less batch loss from oiling out or ambiguous end-points. Especially in continuous crystallizer runs, our technicians observe steadier throughput compared to more variable-and problematic-cousins in the pyridine family.
We rarely talk about safety as pure compliance. Our history with this compound stretches back to days before routine dust monitors or comprehensive PPE programs. Operators now follow strict protocols, using local exhaust ventilation, fitted dust masks, and gloves rated for fine halogenated powders. On more than one occasion, ignoring these basics has led to everything from mild respiratory irritation to skin sensitization. Training goes well beyond formal EHS standards—it draws on practical stories, near misses, and lessons that shape a respect for these materials.
Spill prevention and waste management drive operations strategy. The acid—while not volatile—reacts with strong bases and rapid oxidation agents, requiring careful segregation and neutralization protocols. Over the years, incident logs show that controlling dust during packaging and transfer remains the weak link unless the plant enforces strong supervision and routine equipment checks. Staff have introduced closed suction systems for powder transfer, designed in-house and refined after each audit. Even trace residue clean-up gets near-obsessive attention, because cumulative dust buildup presents long-term environmental and worker risks.
Our environmental commitment extends to effluent treatment. Post-production wash water contains halogenated organic traces, which we send through multi-stage carbon filtration and monitored aerobic digestion. In regions tightening regulations around persistent organic pollutants, this practice has spared the plant from costly retrofits and enabled us to maintain essential supply rolls without major downtime. A quick fix never lasts in this kind of setting; each improvement in site housekeeping or containment owes its success to persistent vigilance.
No certificate or checklist replaces the feedback from customers running these products at scale. Shipping out 2,5-dichloro-3-pyridinecarboxylic acid to multinational pesticide plants exposes every weakness in routine testing. Over time, repeated queries about small color shifts or rare crystallite forms pushed us toward full-spectrum product characterizations. Now, our in-plant analytics cover particle size distributions, residual solvent profiling, and deep-dives into trace impurity patterns. When researchers report unexpected reactivity, our lab teams often can link the cause to tiny variances in moisture or solvent residue, and we close the production feedback loop by tweaking upstream processes.
Stable processing means little without transparent documentation. Our SOPs, batch logs, and traceability records undergo routine review not just by QA but by the production staff who rely on these results to keep lines moving. Rework and deviation investigation often involve multiple teams—what starts as a minor analytical outlier sometimes flags a bigger issue, and every plant veteran has tales of small numbers masking big process bottlenecks.
In dealing with regulatory bodies or customer auditors, we lean heavily on firsthand data—chromatograms, batch certifications, photographic evidence of product morphology. That natural drive toward proof, not promises, defines our culture around 2,5-dichloro-3-pyridinecarboxylic acid. Internally, this means systematic root-cause hunts for any off-spec batch, reinforced by regular cross-functional debriefs to make sure lessons don’t evaporate when staff change roles or shifts.
Success on the customer side rarely turns on isolated lab numbers. Often, we hear from users about subtle differences in batch handling or unexpected results in pilot lots. Each of these cases becomes a springboard for change. Some blends benefit from reduced particle size; others need heightened purity to meet specific emission standards. Our monthly production meetings review these requests and results, feeding what we learn directly into future campaigns.
Direct collaborations between our R&D group and client formulation chemists frequently highlight the fine line between what works in the lab and what fails at scale. A herbicide R&D manager once reported problems with caking during large-scale tableting. Drawing from our own packaging trials, we recommended slight moisture control adjustments, and dedicated packing rooms to limit airborne transfer. The problem vanished on the next campaign. These anecdotes, strung together, drive our evolution—not just of 2,5-dichloro-3-pyridinecarboxylic acid, but our mindset across all similar products.
Long-term partners sometimes request custom batch modifications—tighter sieving, adjusted crystalline morphology, or ultra-low metal content. Our staff have become experts at translating a sketchy application note into tangible changes. Often, what starts as a niche improvement ends up mainstream, as other customers gravitate toward proven reliability gains. Flexibility in process design means we can validate and incorporate feedback within weeks, not months, further tightening the producer-user cycle.
Looking ahead, regulatory shifts and market trends suggest a persistent need for careful tracking and traceability. Our ongoing investment in digitized batch records, improved raw material sourcing, and process automation reflects these realities. The compound’s use in ever-stricter regulatory regimes—be it new EU REACH guidelines or expanded scope within EPA review—pushes us to stay nimble in our control strategies. We see increased demand for lower residual solvents and documentation supporting lifecycle analyses. Every adjustment brings new insight, from solvent substitution efforts to green chemistry pilot runs.
Sustainability pressures now shape even the basics of how we select and run equipment. Energy efficiency audits, waste minimization, and closed-loop water reuse programs form much of our infrastructure investment. None of these alterations would stick without buy-in from the ground floor—so continuous operator training, incentive programs, and real-time data sharing play a steady role in keeping everyone aligned.
Adapting to the needs of small research labs, regional agrochemical blenders, and global multinationals keeps us sharp. The wide range of demand, plus new materials testing from innovative firms, brings a range of challenges. Each batch moves through checkpoints shaped by past hiccups and present requests. Our staff see firsthand how even minor changes on our end can ripple through entire supply chains.
Decades of hands-on production have taught us that behind every order for 2,5-dichloro-3-pyridinecarboxylic acid lies a series of technical bets. Customers use this core building block to push boundaries in their fields—whether they are developing a new herbicide, pharmaceutical intermediate, or specialty polymer additive. Each improvement in our process, each batch record review, and every line tweak directly impact our partners’ outcomes.
We take pride in the role our staff play, not just as operators or quality experts, but as frontline troubleshooters. When problems occur, response draws not from manuals alone, but from years of trial, error, and shared knowledge. This expertise forms the foundation of reliable supply, and it supports those who count on getting consistent, well-characterized 2,5-dichloro-3-pyridinecarboxylic acid every time, no matter how they put it to use.