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HS Code |
440448 |
| Chemical Name | 2,3-Dichloropyridine-4-carboxaldehyde |
| Molecular Formula | C6H3Cl2NO |
| Molar Mass | 192.00 g/mol |
| Cas Number | 142912-42-5 |
| Appearance | Light yellow to brown solid |
| Melting Point | 61-65 °C |
| Density | Approx. 1.5 g/cm³ |
| Purity | Typically ≥ 97% |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Storage Conditions | Store in a cool, dry place, protect from light |
| Pyridine Ring Position Substitution | Chlorine at 2 and 3 positions, formyl at 4 position |
| Smiles | C1=CN=C(C(=C1Cl)Cl)C=O |
As an accredited 2,3-Dichloropyridine-4-carboxaldehyde 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, tightly sealed with a screw cap, labeled for 2,3-Dichloropyridine-4-carboxaldehyde, includes hazard warnings. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for 2,3-Dichloropyridine-4-carboxaldehyde ensures secure drum/pallet packaging, optimizing safety, stability, and maximum space utilization. |
| Shipping | 2,3-Dichloropyridine-4-carboxaldehyde is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported as a hazardous chemical, following all regulatory guidelines for handling and labeling. Appropriate safety data and documentation accompany the shipment to ensure safe storage and handling during transit. |
| Storage | 2,3-Dichloropyridine-4-carboxaldehyde should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Protect from direct sunlight and moisture. Ensure it is kept in a designated chemical storage cabinet, preferably under inert atmosphere if sensitive, and clearly labeled to prevent accidental misuse. |
| Shelf Life | Shelf life of 2,3-Dichloropyridine-4-carboxaldehyde: Typically stable for 2-3 years when stored in a cool, dry, and airtight container. |
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Purity 98%: 2,3-Dichloropyridine-4-carboxaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and contamination-free final products. Melting Point 84°C: 2,3-Dichloropyridine-4-carboxaldehyde with a melting point of 84°C is used in fine chemical research, where controlled melting facilitates precise reaction conditions. Molecular Weight 178.00 g/mol: 2,3-Dichloropyridine-4-carboxaldehyde of molecular weight 178.00 g/mol is used in agrochemical precursor production, where accurate molecular mass supports exact formulation standards. Stability at 25°C: 2,3-Dichloropyridine-4-carboxaldehyde with stability at 25°C is used in storage and handling for industrial synthesis, where material integrity is maintained over extended periods. Particle Size <50 μm: 2,3-Dichloropyridine-4-carboxaldehyde with particle size less than 50 μm is used in catalyst preparation, where fine granularity improves dispersion and catalytic efficiency. Low Water Content <0.5%: 2,3-Dichloropyridine-4-carboxaldehyde with water content below 0.5% is used in moisture-sensitive organic transformations, where minimized hydrolysis risk enhances consistency of end-products. Assay ≥99%: 2,3-Dichloropyridine-4-carboxaldehyde with an assay of at least 99% is used in high-precision analytical applications, where high assay guarantees reproducible and reliable analytical results. Thermal Stability up to 120°C: 2,3-Dichloropyridine-4-carboxaldehyde with thermal stability up to 120°C is used in high-temperature synthetic processes, where it resists decomposition to retain functional performance. |
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Working in the chemical industry, certain building blocks catch attention not just for their reactivity, but for the doors they open in synthesis. 2,3-Dichloropyridine-4-carboxaldehyde represents one such intermediate. Every kilogram we produce reflects years spent refining pyridine derivative processes and the efforts of teams keenly focused on efficiency, stability, and safety. Our experience provides insight into how this compound functions outside brochures or standard data sheets.
Among pyridine-based aldehydes, the 2,3-dichloro substitution pattern on the ring and the carboxaldehyde group at the 4-position create a different reaction profile. Our plant follows a chlorination sequence that gives precise control over isomer formation, ensuring consistency batch after batch. The model available through our production relies on years of tweaking temperature, pressure, and solvent conditions, resulting in a product that handles both scale and sensitivity without surprises. Analysts and project leads alike favor this compound for the sharp, persistent reactivity at the aldehyde group, matched with stability under correct storage.
Our experience shows that supplies can sometimes arrive at the customer with slight off-color or reduced purity. We tackled this by upgrading distillation steps and adopting more robust purification controls as demand increased. In our shipments, the product emerges as a pale yellow solid, with a purity level aimed at exceeding 98% GC, rarely drifting beyond this unless interrupted by upstream raw material fluctuations. We approached packaging with practical sense—containers seal against both ambient humidity and oxygen, keeping spoilage away. Our own internal stability trials keep a close eye on changes, especially under temperature cycling often seen in warehouse environments.
This compound behaves reliably during scale-up, where bench methods don’t always translate upwards. In pharmaceutical research circles, requests come for it as a key starting material toward newer pyridine-based heterocycles and potential drug intermediates. Few aldehydes in the pyridine family respond as smoothly to nucleophilic additions and cyclization steps, which synthetic chemists appreciate as a time-saver. Some agrochemical programs—ones we’ve collaborated with directly—use it for rapid construction of advanced intermediates, especially where chlorinated motifs offer biological effects not found elsewhere.
The real value emerges in its selectivity. The dichloro pattern blocks unwanted side reactions on the pyridine ring, reducing byproducts during coupling or condensation. Compared with 2-chloropyridine-4-carboxaldehyde or the 3,5-disubstituted analogs, yields run higher, and clean-up takes less solvent.
From the plant view, a comparison across related products teaches many practical lessons. In production of simple 4-pyridinecarboxaldehyde, purification fights against ring-opening products and resinification that clog columns. 3,5-disubstitution can protect the ring but complicates post-reaction manipulation, and isolating pure product slows shipments.
The 2,3-dichloro version handles process rigors well; crystallization is more straightforward, and problems like resin build-up occur less. Technicians say the behavior during drying and storage outpaces other aldehydes. Downstream, our partners in contract manufacturing say the dichloro product offers better shelf life and lower risk of autocondensation, giving more predictable outcomes especially under basic conditions.
We encountered some hurdles that regular users—especially in scale-up—might not foresee. Early batches revealed how sensitive the aldehyde group can be to over-chlorination, giving rise to polychlorinated impurities that challenged both isolation and waste handling. UV-Vis and HPLC fingerprints helped pinpoint adjustment of chlorination rates. Another real-world issue was disposal; some waste solvents ended up with traces of unreacted material, so extra step filtration became mandatory in our workflow.
On temperature stability, once a batch faces conditions above 40°C for extended periods, the risk of minor decomposition grows. Quality control teams routinely monitor for changes in IR peaks associated with aldehyde loss or pyridine ring breakdown products. The lessons learned here prompted us to reinforce the cold chain for longer overseas shipments, and we now double-check all packaging for insulation integrity.
In the hands of chemists, real utility translates into reproducibility and process savings. Some of our customers in the custom synthesis community report that the dichloro-aldehyde can tolerate longer exposure to condensation partners without rapid darkening, which is a common complaint for competing chlorinated pyridine aldehydes. The ability to run room temperature condensations over several hours without fearing product degradation saves both time and rework.
Industrial customers often share feedback on filtration behavior after work-up. Compared with mono-chloro analogs, cakes filter cleaner and faster, reducing the need for secondary washes and boosting throughput. These differences stem from subtle solubility quirks of the 2,3-dichloro motif and improved particle morphology, which we can trace back to our optimized crystallization cycle.
The specificity of this aldehyde unlocks synthesis routes that would otherwise stall at the selectivity stage. Medicinal chemists—pushing design boundaries for new chemical entities—prefer this intermediate where selectivity matters more than sheer reactivity. Its compatibility with amine and hydrazine reagents, leading to new heterocyclic cores, enables projects to move from concept to preclinical scale at a practical pace. Because the dichloro groups limit unwanted over-reduction or polymerization, the work-up remains cleaner and less labor-intensive.
In our ongoing research, iterative improvements arise not only from lab data; operator feedback and customer insights drive continual process changes. On more than one occasion, switching solvents or tweaking cooling cycles in response to field requests shaved days off total lead time. These back-and-forth exchanges prove that a reliable supply of 2,3-dichloropyridine-4-carboxaldehyde supports research and industry in more than a theoretical sense—it keeps projects running where others stall.
Regulations on chlorinated intermediates demand both vigilance and transparency. Our facilities run regular environmental risk reviews, and compliance teams keep MSDS documents current and accurate; this avoids both internal delays and downstream clearance issues for customers shipping overseas. In handling, operators wear protection against skin contact and vapor, as even brief exposure can create irritation, a fact learned during the ramp-up years before containment upgrades.
Logistics teams plan shipments with real-world handling risks in mind. Double-lined drums and in-line desiccants reflect the necessity of keeping air and moisture away. Few suppliers have experience scaling handling protocols for such volumes, but years of continuous feedback—not just engineering—brought our standards to current levels.
For customers receiving shipments, real challenges often center around storage and transfer. We recommend not just dry storage but also limiting ambient light, as UV exposure, even from warehouse lights, prompts slow breakdown in some lots. Direct transfer into inert-atmosphere containers upon delivery preserves integrity for longer projects.
Some users reported clumping in portions stored at fluctuating temperatures; tackling this required revising granulation conditions and adding extra checks at the drying step before final packaging. By investing in stainless drying trays and reworked airflow systems, we nearly eliminated caking, cutting solution preparation time in downstream batches.
Another practical tip from regular users has been batch dilution under nitrogen for immediate processing. This skips direct weighing of the solid and streamlines the workflow for continuous runs, especially at kilo scale. We also fielded questions about cleaning trace residues from glassware; mild base solutions clear up carryover before the next campaign.
Often overlooked, process repeatability sits at the core of large-scale production. Every time we review rejected lots or out-of-spec returns, the chain of events usually tracks back to unnoticed process drift—slight temperature lag, a valve not fully seated, or a delay in work-up. Our shift managers prioritize quick interventions over long investigations, aware that many hours lost in troubleshooting ripple outward to customer schedules.
Consistency in color, melting point, and spectral signature defines quality for the synthetic chemist. Those in process validation see real benefit from the stepwise QC regimen we run: on-the-spot GC, followed by trace water analysis and regular third-party cross-checks for peaks in the low ppm range. These checks don’t just exist for compliance; they take uncertainty out of high-stakes projects where a failed batch makes or breaks an R&D timeline.
Early runs produced more mixed-halide byproducts than we expected, causing both purity headaches and downstream waste. Trials with alternate chlorinating agents, switching from thionyl chloride to NCS when the reaction called for milder conditions, cut down byproducts. Improvements in reflux control and solvent recovery lowered costs and kept waste streams more manageable. Shift engineers who watched equipment cycle hundreds of times know these small steps add up to smoother day-to-day operation and more reliable product.
Lessons from reactors, centrifuges, and drying rooms shape our workflow and strategy. At pilot scale, we saw how small leaks or trace oxygen threw off yields. Those early problems led to the installation of low-oxygen glovebox charging stations, which now serve every large batch. Operators follow a running log that flags any drift from the norm. Data capture has played an increasing role—real-time analytics, machine learning anomaly tracking—yet the skilled eye of an experienced technician often catches the single off-spec sample that triggers a full batch review.
Modern manufacturing cannot ignore regulatory and environmental responsibilities. Our solvent use policy favors recyclability and precise containment, with regular audits aimed at both compliance and true minimization of chemical footprint. Chlorinated byproducts run through several stages of separation and capture before neutralization, and heat recovery units trim down both costs and emissions.
Container design, often overlooked, reflects years listening to shipping department feedback. Every drum shipped now includes robust liners and labels, indicating both hazards and optimal handling in plain language. Customers on different continents face varying climate and transit challenges, and containers have adapted accordingly—robust enough for sea transit, light enough for manual handling at smaller docks.
Collaboration drives both our reliability and improvement. Customers often request documentation tweaks, stability data, or advice on handling unique to their process or country. These conversations often highlight future needs—increased sensitivity, larger lot sizes, or regulatory shifts—and we fold that feedback into each yearly planning session. More than once, a suggestion from the floor led to upgraded cleaning, new analytical runs, or tweaks in process scheduling that short-circuited outages on both ends.
This dialogue shapes lab work as much as the engineering schedule. Tweaks suggested by daily users—finer granulation for improved weighing, slower cooling for cleaner crystallization—show up within months rather than years. Reliable supply doesn’t happen by accident; the open loop between manufacturer and end user sits at the heart of every successful campaign.
Markets for 2,3-dichloropyridine-4-carboxaldehyde shift as new applications arise—biotech, specialty materials, even electronics. Each new segment brings a wave of questions: solubility in new solvents, compatibility with exotic reagents, or shipping in ever-larger drums. Our teams run pilot campaigns in collaboration with innovators, testing boundaries of our own methods to match changing needs.
As capacity rises, improvements follow—higher throughput without sacrificing purity, innovations in byproduct minimization, and closer on-site links between synthesis and quality labs. We track how new regulatory debates, such as those affecting persistent chlorinated compounds, prompt us toward greener chemistry and even alternate feedstocks. Product stewardship, in real practice, means not just box-ticking but acting early to foresee and solve upcoming challenges.
The story of 2,3-dichloropyridine-4-carboxaldehyde is not only of a specialty intermediate but of the learning, adjustment, and improvement cycle that drives modern chemical manufacturing. From the reactors to the loading docks, every insight gained from challenges or errors works its way into tighter procedures, better training, and more responsive partnerships with users. Absorbing lessons from production and adapting over time, our facility aims not just to supply a chemical, but to support every project, milestone, and new idea that this intermediate helps realize. Our journey mirrors the evolving needs of science and industry—a process grounded in careful listening and relentless, practical refinement.