2-Chloro-5-nitropyridine-3-carboxylic acid

    • Product Name: 2-Chloro-5-nitropyridine-3-carboxylic acid
    • Chemical Name (IUPAC): 2-chloro-5-nitropyridine-3-carboxylic acid
    • CAS No.: 884494-02-6
    • Chemical Formula: C6H3ClN2O4
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
    • Price Inquiry: sales7@bouling-chem.com
    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    754162

    Product Name 2-Chloro-5-nitropyridine-3-carboxylic acid
    Cas Number 884494-38-2
    Molecular Formula C6H3ClN2O4
    Molecular Weight 202.55
    Appearance Yellow crystalline powder
    Melting Point 190-195°C
    Solubility Slightly soluble in water; soluble in DMSO
    Purity Typically ≥98%
    Storage Conditions Store at room temperature, keep container tightly closed in a dry and well-ventilated place
    Synonyms 2-Chloro-5-nitro-3-pyridinecarboxylic acid
    Inchi Key WWMSJQNRTOHPOF-UHFFFAOYSA-N
    Smiles C1=CN=C(C(=C1[N+](=O)[O-])C(=O)O)Cl

    As an accredited 2-Chloro-5-nitropyridine-3-carboxylic acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed in a 25g amber glass bottle with tamper-evident cap, labeled with chemical name, hazard warnings, and supplier information.
    Container Loading (20′ FCL) 20′ FCL: Typically loaded with 12–14 MT in 25 kg bags or fiber drums, maximizing capacity for efficient chemical transport.
    Shipping 2-Chloro-5-nitropyridine-3-carboxylic acid is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is packed according to standard hazardous material regulations, ensuring minimal risk during transport. The shipment is labeled with proper chemical identification and hazard warnings, complying with local and international shipping guidelines.
    Storage **2-Chloro-5-nitropyridine-3-carboxylic acid** should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep away from incompatible materials such as strong bases and oxidizing agents. Store at room temperature, and ensure proper labeling to avoid accidental misuse. Follow all relevant chemical safety and storage guidelines.
    Shelf Life 2-Chloro-5-nitropyridine-3-carboxylic acid is stable under recommended storage conditions; shelf life is typically 2-3 years.
    Application of 2-Chloro-5-nitropyridine-3-carboxylic acid

    Purity 98%: 2-Chloro-5-nitropyridine-3-carboxylic acid with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and process reproducibility.

    Melting Point 185°C: 2-Chloro-5-nitropyridine-3-carboxylic acid with a melting point of 185°C is used in agrochemical active ingredient production, where thermal stability enhances formulation integrity.

    Molecular Weight 188.54 g/mol: 2-Chloro-5-nitropyridine-3-carboxylic acid at 188.54 g/mol is used in heterocyclic compound design, where precise molecular integration improves target specificity.

    Particle Size < 50 μm: 2-Chloro-5-nitropyridine-3-carboxylic acid with particle size under 50 μm is used in catalyst preparation, where fine dispersion increases catalytic efficiency.

    Stability Temperature 100°C: 2-Chloro-5-nitropyridine-3-carboxylic acid stable up to 100°C is used in chemical process optimization, where it maintains chemical integrity during reaction scaling.

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    Certification & Compliance
    More Introduction

    Introducing 2-Chloro-5-nitropyridine-3-carboxylic Acid: Our Perspective as the Manufacturer

    Chemistry shapes everyday life, often behind the scenes. As manufacturers deeply involved with the molecules we produce, we see 2-Chloro-5-nitropyridine-3-carboxylic acid not just as a catalog item, but as a dynamic building block across research and industry. Our direct experience—from synthesis all the way to packing—gives us special insight into what this compound offers, why chemists depend on it, and how its performance compares with alternatives.

    What Sets 2-Chloro-5-nitropyridine-3-carboxylic Acid Apart

    Blending three functional groups on a single pyridine ring, this compound stands out in the labs and workshops that work on heterocyclic chemistry. The chloro, nitro, and carboxylic acid moieties arrange themselves at distinct positions, which opens up possibilities for precision synthesis. Many chemists working at the cutting edge of pharmaceuticals or advanced material science choose this molecule for routes that demand strong directing effects and specific reactivity.

    Other pyridine derivatives cannot easily match the fine balance here. For example, 2-chloropyridines often serve well in nucleophilic substitution, but rarely carry the activating pull offered by the nitro group at the 5-position. Similarly, the carboxylic acid at the 3-position provides access to transformations—like amide coupling or esterification—that simpler nitropyridines do not support as efficiently. As a manufacturer, every stage helps us appreciate this balance: small shifts in synthesis step conditions can impact purity or yield, testifying to the molecule’s structural precision.

    Direct Experience: Synthesis and Quality Control

    Formulating this compound starts with the careful introduction of the chloro and nitro groups onto the pyridine scaffold. The specified order and the purity of the starting materials control outcomes further down the line. Unchecked impurities result in unwanted side products, eventually creating headaches for end-users trying for reproducible results. It is not uncommon to see requests for specifications tighter than the industry standard, and our plant’s feedback loop between lab and production floor means we refine steps—such as temperature triggers or reagent timings—based on hands-on results.

    Our team tests every lot with detailed HPLC and NMR to ensure that isomeric purity meets the expectations of researchers and industrial chemists. A common headache in this chemistry involves the possible positional isomers—any molecule sent with 2-chloro-3-nitropyridine-5-carboxylic acid (an easy swap for a non-meticulous process) loses guarantee of outcome. Authentication at each stage protects those doing downstream work.

    Specifications Backed by Application Requirements

    Each request for 2-Chloro-5-nitropyridine-3-carboxylic acid comes with different expectations. Many academic users want material with greater than 98% purity to avoid the time price of extra purification. Industrial customers sometimes ask for higher thresholds, especially if developing active pharmaceutical ingredients or complex agrochemicals. Moisture sensitivity plays a role — not all packaging protects as it should — so we opt for custom barrier packaging depending on the average transit time and storage climate for each geography. Stabilizers are not simply added as an afterthought: they come with tested compatibility, making sure the molecule arrives in its desired state, ready to enter the next step.

    Particle size distribution matters less for this product than it does for others — it dissolves rapidly in the polar solvents typically used and usually participates in solution-phase chemistry. Where filtration, isolation, or milling rises in importance, we select the best grinding and screening processes, always under nitrogen, to avoid even trace hydrolysis that can result in loss of the carboxylic group.

    End Uses: Why Customers Choose This Molecule

    Pharmaceutical chemists appreciate the molecule’s directness as an intermediate. Its structure lends itself well to the construction of complex drug candidates, particularly kinase inhibitors and other small molecule drugs that require both electron-poor and electron-rich regions on the aromatic core. We have seen more than one research scientist confirm: substituting a carboxylic acid for a different group at position 3 shifts target activity or metabolism in animal studies. Our own customer support line regularly gets requests for custom derivative synthesis based on the 2-chloro-5-nitropyridine-3-carboxylic acid nucleus.

    Crop protection researchers make use of the selective reactivity. Aromatic chlorides can take part in cross-coupling, while the nitro group gives useful chemistry for reduction or further substitution in later steps. We routinely answer technical queries from customers seeking alternative protection strategies for the acid group to meet their synthesis goals, and sometimes set aside small batches for those working with radioisotope labeling. These industries demand not just purity but confidence in trace metal content and residual solvent profile, so we run extra GC-MS and ICP-MS tests regularly.

    Comparison with Related Products

    Not everyone starts their route with 2-Chloro-5-nitropyridine-3-carboxylic acid. We field questions from partners considering other pyridine carboxylic acids or nitro-substituted heterocycles. Each boasts unique features, but the trio of reactivity—chlorine, nitro, carboxyl—in one ring remains a key differentiator. For instance, 2-chloro-5-nitropyridine lacks the handle for direct amidations or esterifications that the carboxylic group enables. The minor cost difference between starting with our product versus a simpler intermediate saves time and money further along, particularly where one-pot reactions or sequential functionalizations cut the number of purification steps.

    We encourage teams to request samples of both 2-Chloro-5-nitropyridine-3-carboxylic acid and close analogs to see efficiency gains themselves. Years of process feedback suggest that, while unit cost may run slightly higher, the decrease in batch failures, coupled with more consistent product quality, justifies the investment. The flexibility this single compound offers often reduces the number of route changes and regulatory checks, an especially relevant concern in pharma and agrochemical scale-up projects.

    Challenges and Lessons Learned in Manufacture

    Chemists coming from a purely distribution or research background don’t always see the manufacturing nuances—tight pH control, batch vs continuous flow differences, or purification bottlenecks. Scaling this molecule means facing pressure on both cost and compliance, handling both chlorinating and nitrating agents safely, and ensuring effluent treatment matches updated regulations. Even minor raw material variation from upstream partners sometimes forces recalibrations or repeat reaction optimization studies. Our team approaches these issues as practical problems to be solved, leaning on years of multi-product synthesis expertise.

    Maintaining batch-to-batch uniformity can strain a production schedule during global raw material supply fluctuations. During recent disruptions, we took steps to build buffer inventory without sacrificing quality, check new supplier analytical profiles rigorously, and invest in real-time monitoring for impurity levels. Our in-house development chemists review process change requests monthly, focusing efforts on efficiency boosts that do not chip away at user confidence.

    Environmental and Worker Safety Practices

    Handling compounds with both chloro and nitro groups brings specific hazards. Our manufacturing floor uses closed system handling and active scrubber systems to protect operators and limit emission release. We’ve observed that older plant designs without these controls led to minor but real exposure risks—sometimes not flagged until careful workplace air monitoring. Over the years, we built redundancies into our process air and discharge treatment systems, reducing off-site impact and improving plant morale. Compliance isn’t just a checkbox; operators who know they can bring safety observations directly to process engineering create a cycle of real improvement.

    Waste minimization for this chemistry involves more than standard aqueous workups. Salt treatment protocols must be fine-tuned to handle both nitro and chloride content, which can interact in unpredictable ways with certain organic residues. Our site invested in piloting solvent recovery and in-line acid neutralization units, cutting effluent discharge by half. The result means both cleaner water streams and reduced regulatory fees—benefits which long-term customers value, especially those with their own downstream environmental audits.

    Continuous Process Improvement Based on Real-World Use

    Feedback from users—whether academic groups, contract research organizations, or multinational pharmaceutical firms—shapes how we produce, pack, and ship 2-Chloro-5-nitropyridine-3-carboxylic acid. Early on, we discovered that simple desiccant packets did not provide sufficient shelf stability for overseas shipments. Test shipments gave variable results depending on seasonal climate differences between point of manufacture and destination labs. In response, we adapted both the drying step pre-pack and switched to specialty vapor barrier liners. This sort of incremental improvement often pays unexpected dividends, such as reducing cake formation in the bottle and saving customers from tedious powder break-up before weighing out.

    Process modifications never run in isolation. Introducing a new purification method to reduce heavy-metal traces brought a surprise upside: lower color contamination on re-exposure to air, which a group of medicinal chemistry customers reported as a significant practical win. Similarly, recipe tweaks designed to shorten filtration and washing steps also cut down on wash solvent use, a perk rarely noticed outside the plant but significant for greener manufacturing.

    Logistics, Packaging, and Traceability

    Supplying specialized molecules to global destinations means paying attention to more than reaction conditions and product quality. Customers have pointed out inconsistencies in paperwork, customs clearance delays, and variable lead times from other suppliers. We learned early on that direct tracking of each batch from raw material to finished bottle, with full analytical data maintained from start to finish, helps nip misunderstandings in the bud. Customers need to trust that what is written on the label matches what’s in the bottle—every time, for every order.

    Most shipments travel as solids in amber glass, with high-integrity seals and tamper-evidence built in. Where customers ask for larger pack sizes or custom solutions for high-volume pilot trials, our support teams connect plant and shipping managers directly with end-users. This maintains a real-time feedback channel, ensuring quick resolution if unexpected transit temperature excursions or customs hang-ups threaten product stability or delivery timing.

    Industry Trends Affecting 2-Chloro-5-nitropyridine-3-carboxylic Acid Demand

    Recent years saw rapid advances in medicinal chemistry and specialty agrochemicals, with increasing interest in niche heterocyclic scaffolds. Regulatory scrutiny shifted expectations for trace impurity levels and solvent residues, prompting both customers and manufacturers to adopt higher standards. Markets in North America and Europe often ask for more complete impurity profiles and require validation against food-chain or pharmaceutical pathway needs. Our plant adapted to run extra analysis and produce documentation in local languages as part of order fulfillment—not as an extra, but as a built-in expectation.

    Pharma clients, in particular, route more projects through mass customization, rather than bulk commodity synthesis. Smaller, more complex batches make it critical for us to maintain flexible manufacturing schedules and responsive process engineering. We shifted staff training and plant floor layout to ensure we could switch between multi-kilo and gram-scale runs without compromising analytical attention to detail.

    Supporting Innovation, Not Just Supply

    Manufacturers can fall into the trap of pushing stock product. We see our job as more than that: supporting creativity and technical breakthroughs. Whether a team is exploring new reaction pathways, developing novel compound libraries, or conducting environmental fate studies, a reliable supply of quality material unlocks project momentum. Most recently, a collaborative project with an academic team required not just prompt shipment but regular batch sample sharing and help with interpretation of complex NMR data. This kind of exchange led to practical process tweaks that we then folded into our standard recipes, benefiting both research and routine commercial output.

    Supporting early-stage innovation also means being ready to produce variants—protected acids, isotopically labeled versions, or specific salt forms. We welcome custom synthesis challenges, provided we can guarantee the same level of quality control and regulatory compliance as with our standard product. The return is twofold: our own chemistry staff learn from diverse synthetic questions, and customers gain a smoother route to publication or market introduction.

    A Commitment to Reliability and Technical Transparency

    The best partnerships grow through trust built over time. Too many customers have told us stories of receiving poorly characterized material, unpredictable supply, or non-existent technical support from other channels. We never treat traceability and transparency as formalities—each product batch is treated as a new opportunity to prove our commitment to reliability.

    Analytical support continues after delivery, with our technical services team standing ready to talk through any result or method adaptation. As regulatory climate shifts or new requirements evolve, we adapt analytical suites and documentation, aiming always to help customers stay ahead of compliance and keep projects running without interruption. For chemists, timely response to method development questions or data requests often spells the difference between hitting and missing critical project deadlines.

    Closing Perspective: Manufacturing as Partnership

    What matters most, from our perspective as the manufacturer, is not just selling a molecule but supporting those who use it. 2-Chloro-5-nitropyridine-3-carboxylic acid, with its constellation of functions, continues to open up new routes in pharmaceuticals, agrochemicals, and material sciences. Working hands-on with bench chemists, procurement teams, and scale-up process engineers keeps us tuned both to challenges and opportunities. Each lot bears the learning of the one before; every technical support answer, every feedback call, shapes the next batch and the next improvement.

    Through decades of synthesis experience, careful quality control, and a dedication to learning from the field, we continue to refine not just the chemistry of one product, but the way dependable supply and technical partnership drive discovery for everyone using our materials.