5-nitropyridine-3-carboxylic acid

    • Product Name: 5-nitropyridine-3-carboxylic acid
    • Chemical Name (IUPAC): 5-nitropyridine-3-carboxylic acid
    • CAS No.: 21220-14-4
    • Chemical Formula: C6H4N2O4
    • Form/Physical State: Solid
    • Factroy Site: No.968 Jiangshan Rd., Nantong ETDZ, Jiangsu, China
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    • Manufacturer: Nantong Acetic Acid Chemical Co., Ltd.
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    Specifications

    HS Code

    945551

    Name 5-nitropyridine-3-carboxylic acid
    Molecular Formula C6H4N2O4
    Molar Mass 168.11 g/mol
    Cas Number 1975-50-4
    Appearance Yellow solid
    Melting Point 210-214 °C
    Solubility In Water Slightly soluble
    Chemical Structure A pyridine ring with a carboxylic acid at position 3 and nitro group at position 5
    Smiles C1=CC(=NC=C1C(=O)O)[N+](=O)[O-]
    Inchi InChI=1S/C6H4N2O4/c9-6(10)4-1-2-5(8(11)12)7-3-4/h1-3H,(H,9,10)
    Synonyms 5-nitronicotinic acid

    As an accredited 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 Amber glass bottle containing 25 grams of 5-nitropyridine-3-carboxylic acid, sealed with a screw cap and labeled for laboratory use.
    Container Loading (20′ FCL) Container Loading (20′ FCL): 5-nitropyridine-3-carboxylic acid packed in secure drums or bags, optimizing space, ensuring safe, contamination-free transit.
    Shipping **Shipping Description for 5-nitropyridine-3-carboxylic acid:** This chemical is shipped in sealed containers, protected from moisture and light, and labeled according to regulations. It should be transported as a solid chemical reagent in accordance with IATA and DOT guidelines, with appropriate documentation, hazard identification, and handling instructions to ensure safe and compliant delivery.
    Storage 5-Nitropyridine-3-carboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible materials such as strong oxidizing and reducing agents. Protect it from moisture, heat, and direct sunlight. Store at room temperature and ensure the area is free from sources of ignition. Clearly label the storage container for safe handling.
    Shelf Life 5-Nitropyridine-3-carboxylic acid should be stored tightly sealed, protected from light and moisture; shelf life is typically 2–3 years.
    Application of 5-nitropyridine-3-carboxylic acid

    Purity 98%: 5-nitropyridine-3-carboxylic acid with 98% purity is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal impurities in active ingredient production.

    Melting point 176°C: 5-nitropyridine-3-carboxylic acid with a melting point of 176°C is used in fine chemical manufacturing, where consistent thermal stability enhances process reliability.

    Particle size <50 µm: 5-nitropyridine-3-carboxylic acid with particle size below 50 µm is used in catalyst formulation, where superior dispersibility improves catalytic efficiency.

    Stability temperature ≤150°C: 5-nitropyridine-3-carboxylic acid stable up to 150°C is used in advanced material synthesis, where its thermal resistance maintains compound integrity during processing.

    Moisture content ≤0.5%: 5-nitropyridine-3-carboxylic acid with moisture content under 0.5% is used in analytical reagent preparation, where low water content prevents side reactions and enhances accuracy.

    Assay ≥99%: 5-nitropyridine-3-carboxylic acid with assay greater than 99% is used in agrochemical development, where high assay purity produces consistent bioactivity in formulations.

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    Certification & Compliance
    More Introduction

    5-Nitropyridine-3-Carboxylic Acid: Reliable Building Block for Advanced Chemistry

    Understanding Its Value in Modern Applications

    Some chemicals step up as small but vital players in research and manufacturing. 5-nitropyridine-3-carboxylic acid sits in that camp by offering researchers a clean, reproducible starting point for complex syntheses. This compound attracts chemists because it helps bridge critical gaps between basic raw materials and sophisticated pharmaceutical targets.

    Looking at its formula — a nitro group fixed to a pyridine ring with a carboxylic acid arm — the molecule shows promise where designers demand both electron-withdrawing effects and strong solubility profiles. Labs use this versatility every day. The nitro group often draws attention: it tunes the reactivity, guiding selectivity in subsequent steps. The carboxylic acid group, relatively exposed, opens doors for modification — amide bond formation, esterification, or even coupling reactions become straightforward, and that means it rarely stalls out projects because of uncooperative chemistry.

    What the Model Offers

    Clients usually see 5-nitropyridine-3-carboxylic acid supplied as a high-purity, free-flowing crystalline powder. The dominant form hits the sweet spot between stability and synthetic reactivity, storing well on shelves but springing into use when dropped into a round-bottom flask. Specification matter churns up a lot of debate among buyers, and this material typically delivers in the areas people care about: tight purity levels, minimal contaminants, easy handling, and consistent supply batches. Suppliers tend to keep water content low, using trusted drying protocols, since moisture can complicate coupling steps or chromatography downstream.

    In hands-on experience, researchers appreciate materials with good shelf stability and predictable performance across different reactions. Over the years, I never encountered trace heavy metal content that muddied up results; reputable sources screen for this, sparing chemists from scrambling during troubleshooting. Controlled batch-to-batch color and melting point mark out reliable product, and those who use it notice repeatable success, even after the bottle’s been open for months.

    How Researchers Use 5-Nitropyridine-3-Carboxylic Acid

    Synthetic chemistry uses building blocks much the way construction crews use lumber and brick. For anyone hunting for pyridine scaffolds that can survive harsh reactions, few options work as well. Medicinal chemists often reach for this compound to append nitro-pyridyl fragments to drug candidates: either as a direct part of a lead compound or as an intermediate in multi-step syntheses. When medicinal chemistry deadlines loom, reliability shaves days off synthesis. The nitro group’s electron-poor character can prime a molecule for selective nucleophilic attack. At the same time, developers may reduce the nitro group later to yield amine derivatives — a standard trick for expanding a compound’s chemical space.

    The carboxylic acid group stands out as a workhorse in transformations that build up peptide mimics, specialty polymers, and heterocycle libraries. Any bench chemist who’s battled tough coupling reactions knows how a clean, well-behaved acid group keeps purification headaches at bay. Solid-phase chemists have also championed this acid for resin attachments, seeing minimal loading problems. For pharmaceutical intermediates, especially, such dependability gets projects through stringent regulatory checks.

    Different From the Usual Suspects

    Plenty of pyridine carboxylic acids crowd the market, but the 5-nitro flavor brings a mix of reactivity and selectivity rarely matched by simpler analogs. Take nicotinic acid — nice in vitamin chemistry but predictable to a fault. Swapping hydrogen for nitro at the 5 position swings the electronic character: The molecule resists oxidation better, tolerates certain cross-couplings, and helps researchers tailor transformations to their needs. This difference isn’t just academic; it translates into fewer failed reactions and more leeway in exploring reaction pathways.

    The nitro group won’t always find a substitute, either. Chemists often choose between available functional groups, but if you need the kind of control a nitro imparts, you won’t get far swapping in halogens or even other electron-withdrawing groups. Precision matters. In direct comparison experiments, providing 5-nitropyridine-3-carboxylic acid instead of its 3-nitro cousin often produces better regioselectivity or even unlocks previously problematic steps. Some researchers have published on these subtle, but crucial, distinctions, showing how the position and chemistry of the groups dictate both reactivity and biological properties.

    Chemical Supply and Quality Control

    Reliability comes as much from sourcing as from chemical structure. In the chemical industry, inconsistent material can easily derail a whole campaign. Large-scale buyers might expect elaborate certificates and independent validation, but even small-lab purchases now receive the same scrutiny. I’ve reviewed chromatograms for delivered batches and seen tight single peaks dominate product profiles, reassuring users about the level of contaminants. Trace metal analysis and residual solvent checks turn up little beyond the expected. The reality of global chemical supply chains means a few missteps can spoil what should be a seamless ordering experience. Collaborations between academic groups and suppliers have helped grow trust, pushing most producers to adopt stricter QMS (Quality Management System) protocols.

    Human error can never disappear, but the major players track deviations and batch complaints closely. This brings real benefits to buyers: fewer surprises, stronger confidence in critical experiments, and less wasted time. Most scientists care less about certificates than about how the powder behaves during workups — smooth dissolving, no unexpected color changes, and robust melting points show a producer pays attention. That’s where 5-nitropyridine-3-carboxylic acid stands out compared to quick-turn generic carboxylic acids, which sometimes hide unexplained impurities.

    Personal Experience: Working with 5-Nitropyridine-3-Carboxylic Acid

    I came to appreciate this chemical through frustration with lesser versions. Once, while troubleshooting a bottleneck in a multi-step synthesis, I realized the problem lay with a poorly characterized carboxylic acid. Ghost peaks in chromatograms, tacky residue during purification — all clear signs that upstream material wasn’t right. Switching to a reputable 5-nitropyridine-3-carboxylic acid solved the issues, saving me both days of re-work and wasted solvent costs. The clean powder gave crisp melting behavior, and my yields jumped almost overnight.

    Beyond that one crisis, the compound helped streamline a whole suite of reactions: Suzuki couplings stuck, saponifications failed, and I kept circling back to starting materials. Each time I used a version characterized by tighter analytical data and more consistent performance, the headaches faded. Even students with less lab experience reported fewer errors during scale-up or workup.

    Pharmaceutical and Industry Relevance

    The pharmaceutical sector prizes synthetic intermediates that keep options open. Medicinal chemistry projects live and die by the toolkit available to them, and small changes on a pyridine ring can spell the difference between breakthrough or dead end. What I see with 5-nitropyridine-3-carboxylic acid is its use as a staging post: projects targeting kinase inhibitors or anti-infectives regularly build out from this scaffold.

    Even outside pharma, the material finds homes in agrochemical synthesis, specialty dyes, and advanced polymer design. Analytical teams appreciate the ease with which it tracks in both HPLC and TLC, making workflow smoother for QC labs. Small differences — like better color uniformity and less odor — make life easier for technicians on the bench day in, day out.

    Exploring new routes often means taking calculated risks. Substituted pyridines can behave unpredictably under heat or in water-sensitive conditions. In pilot plant trials, a reliable batch of 5-nitropyridine-3-carboxylic acid gives everyone from process chemists to QC managers peace of mind. For scale-up, cleanliness and reproducibility matter as much as reaction speed, especially in multi-kilo deliveries where even traces of impurity gum up reactors or prompt safety concerns.

    Solving Common Problems in Synthetic Pipelines

    With experience, people learn to anticipate bottlenecks linked to poor starting materials. Impure feedstocks create sticky residues, form emulsions during washes, or leave behind spots after chromatography. In these moments, pure 5-nitropyridine-3-carboxylic acid quickly pays for itself: workups go to plan, isolations succeed, staff lose less time in repetitive troubleshooting, and less solvent gets wasted on repeat runs.

    Many chemists test their incoming stock by running small-scale pilot reactions. Consistent results mark a trustworthy material. Labs running on budget constraints appreciate such predictability because it gives leadership confidence to scale research quickly and cut down wastage. I recall a project where quick scaling to multi-gram quantities would’ve been impossible with a struggling, impure precursor — a timely re-order of 5-nitropyridine-3-carboxylic acid from a trusted supplier let us stay on track and deliver the compound library weeks ahead of schedule.

    Improving Access and Advancing the Field

    The chemistry community continues to make headway in access and quality. Over the past few years, more manufacturers have entered the arena, pushing standards and improving education for users. Producers actively seek feedback, update their purification steps, and implement training for their workforce. Such efforts result in fewer customer complaints and stronger relationships between labs and their chemical sources.

    Specialty intermediates once suffered from long lead times and erratic pricing. Now, logistical improvements and increased demand, especially from drug discovery and development groups, help drive down costs and create competitive supply. The upshot for users: improved affordability, rapid sample delivery, and documentation that genuinely supports regulatory filings or journal publication.

    Researchers play their part by sharing both success stories and problems. Publishing details about how certain batches performed or failed helps raise industry standards: the feedback loop encourages producers to be transparent about changes in process, new characterization data, and improvements in analytical rigor. This grassroots improvement matters more than any one safety sheet.

    Environmental and Safety Factors

    As global industries move toward more responsible sourcing, attention turns to every molecule in the lab. 5-nitropyridine-3-carboxylic acid, like most similar chemicals, presents manageable hazards when handled with sensible precautions. Reputable sources share clear, up-to-date safety recommendations, and proper chemical hygiene handles the rest. Proper containment, regular training, and up-to-date labeling make for smooth operations.

    Waste disposal presents a real concern. Extra handling steps — filtration, solvent washes, distillation residues — all impact environmental targets. Facilities that recycle solvents on-site or collect nitro compounds for independent treatment reduce both regulatory risk and costs. Some groups have started collaborating with suppliers to return unused or expired materials, closing the sustainability loop and setting a stronger example for others.

    On the regulatory side, accurate documentation keeps end customers on safe ground. Material data sheets, clear batch tracking, and transparency about residual solvents and byproducts position users to pass audits and meet their obligations. Most research settings now treat these standards as non-negotiable, making everyone’s job simpler.

    Pushing the Limits: Future Directions

    Chemists thrive on possibility. Each improvement in synthetic methodology opens up new lines of enquiry, new molecules, and sometimes new therapies. Having reliable, well-characterized building blocks like 5-nitropyridine-3-carboxylic acid supports innovation by eliminating uncertainty at early stages. Researchers now report using this compound in catalyst and ligand development, where pyridine frameworks underpin advances in organometallic chemistry.

    The next wave may bring customized derivatives, produced at scale with just as much consistency. Demand for green synthesis routes, usually milder and less wasteful, means a push toward bio-based and renewable starting points. Already, some suppliers advertise reduced-carbon options for standard products.

    Industry consortia increasingly pool resources to test new procedures, log analytical results, and identify best practices for scale-up. Open dialogue between chemists and chemical makers helps solve ongoing challenges: optimizing crystal sizes for filtration, fine-tuning solubility to help with handling, and minimizing impurities that can destabilize pharmaceutical intermediates.

    Why It Matters Every Day

    In real-world practice, decisions about starting materials don’t just shape scientific outcomes — they also impact lab morale, project budgets, and the speed at which breakthroughs reach the next milestone. Every shortcut toward cleaner, more reliable input stock creates compounding benefits: project teams deliver results faster; funding goes further; new talent spends time learning science, not chasing ghost problems.

    A few years ago, a colleague told me about a failed drug candidate, its troubles traced back to inconsistent intermediates. The ripple effects meant revisiting months of work and justifying extra costs to funders. Learning from such hard lessons drives people to choose materials like 5-nitropyridine-3-carboxylic acid for their backbone projects. Avoiding false economies up front brings peace of mind — a value hard to measure, but crucial for those aiming high.

    For those running custom synthesis, taking shortcuts on raw materials rarely pays off. In high-throughput screening or combinatorial library work, reliable supply translates into more hits, less noise, and cleaner data for SAR (structure-activity relationship) studies. Graduate students and seasoned researchers alike benefit from tools that just work, day in and day out.

    Choosing Wisely: Key Considerations

    Decision-makers now weigh more than just price or availability. Batch uniformity, traceability, purity, and analytical backing matter as much as prompt delivery. For grant-driven research, documentation often makes or breaks funding extensions. Those who’ve seen their work stumble over unexpected failures prize certainty in every bottle — and 5-nitropyridine-3-carboxylic acid’s consistent performance often sets it above less thorough alternatives.

    Working relationships with suppliers build up over repeat orders and honest communication about standards. Labs willing to provide feedback about particle size, melting point shifts, or reaction failures do themselves and their peers a favor. The best suppliers accept that every batch might prompt questions, and they keep full records to enable productive troubleshooting.

    Legal and compliance questions form a growing part of procurement. With regulations tightening around hazardous shipments and environmental impact, transparent paperwork and proactive safety support now come bundled with reputable products. Research organizations win more support from stakeholders and regulatory bodies when they invest in certified, clearly documented products rather than cutting corners.

    Looking Forward as a Community

    The work of science rests on small steps taken seriously. Each improvement in chemical supply frees up time and energy for teams to invent, analyze, and build new knowledge. 5-nitropyridine-3-carboxylic acid exemplifies this shift toward reliability and rigor. Whether used as a precursor to new medicines, industrial catalysts, or advanced polymers, its track record gives project managers, bench chemists, and QC specialists strong reason to make it a staple on their shelves.

    Community-driven standards have slowly raised the level of performance expected from every vendor. These expectations trickle down, prompting even smaller players in the field to up their game. Researchers must continue sharing their real experiences with each product batch, holding suppliers accountable for quality, and shaping best practice for everyone entering the field. Such collaborations lay the foundation for progress — not just for one chemical, but for the whole research ecosystem.

    With tools like 5-nitropyridine-3-carboxylic acid, today’s labs do more than ever before: safe, confident in their processes, and ready to follow curiosity as far as science allows.