2-Chloro-4-iodopyridine-3-carboxaldehyde

    • Product Name: 2-Chloro-4-iodopyridine-3-carboxaldehyde
    • Chemical Name (IUPAC): 2-chloro-4-iodopyridine-3-carbaldehyde
    • CAS No.: 885276-00-6
    • Chemical Formula: C6H3ClINO
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@boxa-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    100877

    Product Name 2-Chloro-4-iodopyridine-3-carboxaldehyde
    Cas Number 1371582-98-9
    Molecular Formula C6H3ClINO
    Molecular Weight 282.46 g/mol
    Appearance Pale yellow solid
    Solubility Soluble in organic solvents
    Purity Typically ≥ 98%
    Smiles C1=CN=C(C(=C1I)C=O)Cl
    Inchi InChI=1S/C6H3ClINO/c7-6-4(2-10)5(8)1-3-9-6/h1-3H
    Storage Conditions Store at 2-8°C, protected from light
    Hazard Classification Irritant
    Synonyms 3-Formyl-2-chloro-4-iodopyridine

    As an accredited 2-Chloro-4-iodopyridine-3-carboxaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-gram sample of 2-Chloro-4-iodopyridine-3-carboxaldehyde arrives in a sealed amber glass vial with hazard labeling.
    Container Loading (20′ FCL) Container Loading (20′ FCL) for 2-Chloro-4-iodopyridine-3-carboxaldehyde: Typically packed in sealed drums or bags, safely secured for bulk export.
    Shipping **Shipping Description:** 2-Chloro-4-iodopyridine-3-carboxaldehyde is shipped in sealed, inert containers under dry, cool conditions. It should be handled as a hazardous chemical, compliant with regulations for toxic and environmentally hazardous substances. Proper labeling, documentation, and cushioning against shock or moisture are required during laboratory or commercial transport.
    Storage 2-Chloro-4-iodopyridine-3-carboxaldehyde should be stored in a tightly sealed container, protected from light and moisture. Keep in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure the storage location is secure and clearly labeled. Handle with appropriate personal protective equipment to prevent exposure.
    Shelf Life 2-Chloro-4-iodopyridine-3-carboxaldehyde should be stored tightly sealed, protected from light and moisture, with a typical shelf life of 2 years.
    Application of 2-Chloro-4-iodopyridine-3-carboxaldehyde

    Purity 98%: 2-Chloro-4-iodopyridine-3-carboxaldehyde with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high reaction yield and minimal byproduct formation.

    Melting Point 110°C: 2-Chloro-4-iodopyridine-3-carboxaldehyde with melting point 110°C is used in solid-phase organic synthesis, where consistent phase transitions improve process scalability.

    Molecular Weight 282.44 g/mol: 2-Chloro-4-iodopyridine-3-carboxaldehyde with molecular weight 282.44 g/mol is used in heterocyclic compound production, where precise stoichiometry enhances structural accuracy.

    Stability Temperature 25°C: 2-Chloro-4-iodopyridine-3-carboxaldehyde stable at 25°C is used in chemical library storage, where long-term compound integrity is maintained.

    Particle Size <50 µm: 2-Chloro-4-iodopyridine-3-carboxaldehyde with particle size less than 50 µm is used in catalyst preparation, where uniform dispersion increases catalytic efficiency.

    Water Content ≤0.5%: 2-Chloro-4-iodopyridine-3-carboxaldehyde with water content ≤0.5% is used in moisture-sensitive reactions, where reduced hydrolysis preserves functional group activity.

    HPLC Assay ≥99%: 2-Chloro-4-iodopyridine-3-carboxaldehyde with HPLC assay ≥99% is used in analytical research, where purity verification allows for accurate experimental results.

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    Certification & Compliance
    More Introduction

    2-Chloro-4-iodopyridine-3-carboxaldehyde: A Closer Look at an Essential Building Block

    Product Introduction and Context

    Industry demand for niche pyridine derivatives often converges on versatile intermediates like 2-Chloro-4-iodopyridine-3-carboxaldehyde. Over the past years of development and production, our work with this compound has shaped not only how we approach halogenated aromatic systems, but also underscored its importance in fine chemical synthesis, pharmaceutical research, and agricultural chemistry.

    On the surface, the product name suggests a lot—this is not a simple raw material, but a carefully crafted molecule where the placement of chlorine and iodine on the pyridine ring profoundly affects reactivity and downstream utility. We have refined our proprietary synthesis route to control impurities, minimize metal contaminants, and assure the precise location of the functional groups. Through repeated optimization, our team found that minor changes in reaction conditions could create significant differences in product quality, and those learnings persist in every batch.

    Why Molecular Structure Matters

    Substituting at the 2 and 4 positions unlocks selectivity in subsequent reactions. The 3-carboxaldehyde group offers a convenient handle for condensation and coupling, making this compound attractive to research chemists and process engineers alike. In practice, electrophilicity at the 3-position translates into high yields for downstream transformations: the aldehyde reacts readily, yet the electron-withdrawing effects of chlorine and iodine temper overactivity, which reduces risk of side-product formation. This balance is not a given—many similar pyridine derivatives create unpredictable mixtures, leading to wasted time and higher purification costs.

    Years ago, our synthesis pipeline relied on multi-step halogenation that sometimes triggered ring rearrangements or unwanted dimerizations. Tinkering with solvent, catalyst system, and reaction temperature, we landed on protocols that prioritize yield and selectivity. This reduces batch-to-batch variation and offers reliability for scale-up. Methods that rely on less controlled halogenation often leave residual starting material and need extra purification, raising cost and reducing sustainability.

    Specifications Reflecting Real-World Demands

    Before moving a batch off the line, we meticulously check purity through HPLC, confirm structure via NMR, and run trace metal analysis. There is wide variability in pyridine derivatives offered by international markets, but many samples sourced through traders fall short on these criteria. We insist on maximum absorption in the correct NMR shifts and minimal extraneous aromatic signals. For many projects, even trace impurities—such as unreacted starting pyridine or isomeric byproducts—can derail sensitive synthesis steps. Time spent removing what should not be there is time lost in already tight production timelines.

    Moisture content and particle size distribution are no afterthought. Pyridine chemistry can be capricious with hydrolysis, so we store material under inert gas and rigorously test for water by Karl Fischer titration. The decision not to cut corners in drying or packaging comes from experience: past incidents, where slight moisture ingress led to decomposition during transit, cost much more in customer downtime than savings from skipping a drying cycle.

    Applications That Drive Innovation

    Customers commonly use this compound to create pharmacophores for kinase inhibitors or anti-infective agents. Others build agrochemical active ingredients from it, leveraging the selective halogenation pattern to create new modes of action in pest control. In high-throughput medical labs, small quantities integrate into combinatorial libraries for structure-activity relationship studies, capitalizing on how the aldehyde and halogens interact with various lead structures.

    One research collaboration pushed us to optimize enantiomeric selectivity on a downstream transformation, driving us to reach new doability in chiral catalysis. Another project saw the use of our material in creating labeled probes, where the high-purity standard allowed for cleaner radioiodination, reducing waste and radiochemical handling time. These stories highlight just a slice of what becomes possible when users trust both the formulation and sourcing from experienced hands.

    Real Differences From Other Pyridine Derivatives

    Colleagues often ask why choose 2-Chloro-4-iodopyridine-3-carboxaldehyde over something like 2-chloropyridine-3-carboxaldehyde or 2-iodo analogs. The answer usually traces back to dual halogen functionality. The presence of both electron-withdrawing groups on opposite faces of the ring yields unique reactivity patterns. Selective cross-coupling becomes feasible, where the iodine or chlorine can serve as the leaving group depending on ligand, catalyst, and system employed.

    Many buyers only notice the difference after troubleshooting inconsistent coupling reactions or by failing to achieve desired regioisomer ratios. Years of process development and feedback cycles taught us that single-halogen products simply do not provide the same utility for late-stage diversification. Dual halogenation, especially combined with the carboxaldehyde, broadens what is accessible: Suzuki-Miyaura couplings at one position, nucleophilic substitutions at another, and ample headroom for introducing new chemical handles.

    In our experience, cheaper analogs sometimes tempt through lower upfront cost, but create headaches later during scale-up or regulatory submission. Analysts have returned material from other sources that exceeded allowable levels of isomers or residues from process chemicals. We have designed our workflow to anticipate these pitfalls by building in multiple checks. That attention pays off by supporting smoother process validation for customers, especially those operating under cGMP standards.

    Handling and Sustainability Considerations

    Handling halogenated pyridines poses distinct operational risks. Over the years, we designed the layout of our technical plant with spill containment and air handling tailored for volatile aromatics. Operators wear specialized PPE, and we use closed-system transfer for both raw materials and product. Waste management matters, too—halogenated byproducts go through dedicated streams, limiting environmental impact and supporting high standards in regulatory audits.

    Chemical manufacturing shoulders responsibility far past the point of loading drums on a truck. Early in our production history, wastewater issues from unreacted halides drew regulatory scrutiny. Investing in in-house treatment made an immediate difference. Not only did it bring effluent within discharge limits, but it allowed us to reclaim iodine—a cost-saving and resource-recovering measure we never would have realized if just following off-the-shelf recommendations. Every kilogram of iodine recycled counts on the bottom line and reduces dependency on scarce global supply.

    Transport and storage present their own lessons. 2-Chloro-4-iodopyridine-3-carboxaldehyde can degrade with heat and light, so temperature and humidity controls make the difference between material arriving viable or needing rejection. We calibrate storage to local climate, using data loggers and alarmed refrigeration as needed. These steps prevent spoilage and ensure each shipment meets not just our internal standards, but those of our most demanding partners.

    Innovation and Collaboration in Product Development

    Continuous dialogue with partners at universities and downstream customers drives us to constantly revisit process improvement. Chemists ask for tighter impurity specs or explore new derivatization tools, and we respond by reworking synthesis or purification. Just three years ago, a partner’s requirement for ultra-low metal contamination forced a shift away from conventional palladium catalysis—which sent us on a search for alternative catalyst systems, ultimately finding methods that met their needs without adding computational or cost burden.

    As regulatory expectations evolve, so too must our processes. Ensuring traceability, real-time monitoring, and transparent documentation isn’t optional when supplying advanced intermediates to the pharmaceutical sector. Information from analytical checks feeds back into process controls, forming a loop that supports continuous quality improvement. Auditors and inspectors want more than a clean set of specs—they expect demonstrable evidence of control, management of deviations, and commitment to product stewardship.

    Challenges and Practical Solutions in Manufacturing

    Manufacturing 2-Chloro-4-iodopyridine-3-carboxaldehyde is not without its headaches. Starting material availability and purity can swing with market shocks, particularly when sourcing specialty halides. We maintain inventory buffers, qualify secondary suppliers, and adapt to input changes. There are no shortcuts here—failures in quality assurance at the front end lead to snowballing issues on the backend.

    Solvent recovery and emissions management remain tightrope walks. Our plant runs fractional distillation units and activated carbon traps, but upgrades are constant. New filtration and scrubbing technologies help us meet evolving emission limits while keeping process economics viable. By working with local environmental authorities, we have introduced waste minimization audits and learned to re-integrate side-streams into other product lines. Experience has taught us that every extra day spent on upfront process engineering saves weeks of rework and potential non-compliance later.

    On the human resources side, training plant staff in the nuances of handling exotic intermediates pays continuous dividends. Routine troubleshooting, equipment maintenance, and batch documentation set our facility apart. Staff know the difference between maintained and improvised controls, and that pride reflects in the consistency experienced by our long-term partners.

    Customer Experience and Technical Support

    Supplying advanced intermediates goes beyond delivering containers. Researchers and production managers routinely reach out with technical questions—sometimes about reactivity with new ligands, other times regarding shelf-life under layered storage. We dedicate chemists and application specialists to provide answers, not sales pitches. That hands-on culture comes from decades in the lab, where we learned the hard way that every new process uncovers unexpected hurdles.

    Some clients want to trial kilogram-scale batches before committing to full production runs. We encourage these pilot-scale validations, providing full documentation, batch samples, and background on how process history could impact their downstream reactions. Sharing application notes, performance data, and troubleshooting tips reduces friction and aligns teams across the supply chain.

    Regulatory queries about traceability, lot-to-lot variability, or residual solvents are handled directly by people who oversee the manufacturing campaign, not just an administrative support desk. Building trust in today’s tightly regulated climate means showing work with the depth and transparency that experienced users recognize and appreciate.

    Looking Ahead: Market and Scientific Opportunities

    Chemical innovation rarely stands still. As the market for highly functionalized intermediates grows, so do opportunities—and demands—for products like 2-Chloro-4-iodopyridine-3-carboxaldehyde. Growth in precision medicine, the development of new crop protection tools, and advances in material science each present new contexts where this compound finds relevance. We keep an eye on those trends, ready to collaborate and refine production for emergent synthetic targets.

    Nearly every major leap in downstream application links back to carefully engineered building blocks. The expectation goes well beyond simple supply—flexibility, scientific rigor, and real-world troubleshooting make the difference. Years spent behind the scenes, managing challenges and embracing feedback from end-users, shapes our approach far more than following any script or copying existing models.

    With new reaction modalities—like photoredox catalysis and green chemistry mandates—researchers constantly push the boundaries of what halogenated pyridines can do. Keeping our product both relevant and exceptional means never settling for current-state methods. We invest in analytical upgrades, synthesis refreshes, and, most importantly, dialogue with those who put our compounds to the test in new and unexpected ways.

    Conclusion: The Manufacturer's Perspective

    Manufacturing 2-Chloro-4-iodopyridine-3-carboxaldehyde has taught us the value of relentless process improvement, transparent communication, and a direct line to those using the product at the bench or reactor. There is a satisfaction in knowing that deliberate choices throughout production ripple through to more successful experiments, streamlined scale-ups, and regulatory confidence.

    We continue building our capabilities not just because market trends demand it, but because years of experience prove that scientific and operational excellence go hand in hand. A molecule’s impact extends beyond its molecular weight or melting point—what sets it apart is the cumulative expertise and care baked into every step, from raw material sourcing to the very last test before shipping. That philosophy remains at the heart of how we serve chemical innovators today.