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1,6-Naphthyridine-2-Carboxylic Acid

    • Product Name 1,6-Naphthyridine-2-Carboxylic Acid
    • Alias 2-Carboxy-1,6-naphthyridine
    • Einecs 628-014-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    142210

    Productname 1,6-Naphthyridine-2-Carboxylic Acid
    Casnumber 18830-75-6
    Molecularformula C8H6N2O2
    Molecularweight 162.15 g/mol
    Appearance Off-white to pale yellow solid
    Meltingpoint 246-250°C
    Solubilityinwater Slightly soluble
    Smiles C1=CC2=NC=CC(=C2C=N1)C(=O)O
    Inchi InChI=1S/C8H6N2O2/c11-8(12)6-2-1-5-7(10-6)3-4-9-5/h1-4H,(H,11,12)

    As an accredited 1,6-Naphthyridine-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is packaged in a sealed amber glass bottle containing 25 grams, labeled with hazard warnings, product name, and purity details.
    Shipping **Shipping Description:** 1,6-Naphthyridine-2-Carboxylic Acid is shipped in tightly sealed containers to prevent moisture and contamination. It is packaged according to chemical safety regulations, labeled appropriately, and typically shipped at ambient temperature unless otherwise specified. Proper documentation and handling instructions accompany the shipment to ensure safe and compliant transportation.
    Storage 1,6-Naphthyridine-2-carboxylic acid should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of moisture and strong oxidizing agents. Protect it from light and incompatible materials. Label the container clearly, and keep it in a designated chemical storage area, preferably under inert atmosphere if sensitive to air or moisture.
    Application of 1,6-Naphthyridine-2-Carboxylic Acid

    Applications of 1,6-Naphthyridine-2-Carboxylic Acid in Industrial Manufacturing

    As an established producer of 1,6-Naphthyridine-2-Carboxylic Acid, we supply to specialized sectors that require traceable raw materials for downstream synthesis and formulation. The unique heterocyclic structure of this compound enables focused performance in high-value applications, each demanding strict process control, verified compliance, and consistent performance in the final product. Below, we outline several authentic industrial scenarios highlighting where our product integrates into global manufacturing chains.

    1. Active Pharmaceutical Ingredient Intermediate Synthesis

    Pharmaceutical manufacturers use this compound as a key intermediate, particularly for crafting third-generation antibacterial agents and select antivirals. The carboxylic acid group undergoes coupling in the early or mid-stage steps, defining critical chirality and activity for the target API. Sourcing must support batch traceability, impurity profiling, and regulatory documentation. Our process stability supports both pilot and commercial scale synthesis, particularly in regulated markets.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • USP and Ph. Eur. published monographs (if relevant to downstream APIs)
    • FDA 21 CFR Part 210/211 – cGMP for Finished Pharmaceuticals
    • EDQM CEP documentation for controlled intermediates

    Typical usage ratio

    • 0.5–8% of the total input mass in stage-specific synthetic routes; optimized based on molar conversion and target API yield; process chemists adjust based on step economy and impurity load.

    Downstream process integration

    • Introduced during early–intermediate coupling, amidation, or cyclization reactions as a ring precursor or carboxyl functionality source.
    • Used in pressure reactors or jacketed glass vessels under inert conditions.
    • Monitored with in-process HPLC and LC–MS for residuals and purity.

    Final product types

    • Oral and injectable antibiotics
    • Antiviral bulk substances
    • Niche oncology drug candidates (if structure–activity allows)

    2. Fluorinated Agrochemical Building Block

    Producers of selective herbicides and insecticides employ 1,6-naphthyridine-2-carboxylic acid as a ring scaffold for constructing novel actives requiring pyridine functionality and extended plant safety profile. The compound typically enters as a pre-fluorination building block, contributing stability and bioavailability to the final agrochemical ingredient. Application in this segment demands high assay, defined impurity cutoffs, and compliance with agrochemical registration data sets.

    Industry compliance standards

    • OECD Guidelines for the Testing of Chemicals – Section 1 (Physico-chemical properties)
    • ISO 17034 for reference material production (where applicable to analytical standards)
    • REACH Substance Registration (European market)
    • FAO/WHO Specifications and Residue Limits (Codex Alimentarius benchmarks)

    Typical usage ratio

    • 1.2–6.0% as a molar input relative to final agroactive moiety; exact dosage determined by the required substitution pattern and yield of the fluorination or alkylation step.

    Downstream process integration

    • Added in liquid-phase synthesis reactors prior to electrophilic fluorination or cross-coupling.
    • Monitored for ring integrity and conversion completion; side products removed via continuous extraction.
    • Serves as a core for lead optimization in proprietary actives by multinationals.

    Final product types

    • Selective herbicide technical concentrates
    • Environmental insecticide actives
    • Precursor solutions for formulation into EC/SC/WDG crop protection forms

    3. High-Performance Dye and Pigment Synthesis

    Colorant manufacturers incorporate this acid as a foundational unit in the synthesis of specific naphthyridine-based dyes, where chromophore stability and UV resistance are critical. The compound's structure fosters superior lightfastness across textile and plastics applications, and its integration supports precise hue tuning via controlled coupling reactions. Compliance requirements include tight control over color index purity and solvent residue.

    Industry compliance standards

    • ETAD (Ecological and Toxicological Association of Dyes and Organic Pigments Manufacturers) Guidelines
    • ISO 105-X Series for textile colorfastness
    • REACH Annex XVII (for dyes in textile/consumer goods)
    • Oeko-Tex 100 (where relevant for articles in direct skin contact)

    Typical usage ratio

    • 3–15% feedstock input, often as limiting reagent in azo- or anthraquinone-based pigment synthesis; tuned according to color profile and absorption maxima.

    Downstream process integration

    • Entered into coupling or condensation steps after initial aromatic amine activation.
    • Intermediate is purified via crystallization and characterized by UV–Vis and HPLC analysis.
    • Used in both batchwise and continuous synthesis lines for major pigment plants.

    Final product types

    • High-performance organic pigments for engineering plastics
    • Disperse dyes for PET textile applications
    • UV-resistant colorants for automotive and outdoor coatings

    4. Analytical Reagent and Specialty Chemical Synthesis

    Specialty chemical and laboratory supply companies utilize this compound in the multi-step production of analytical reagents, chelating agents, and custom intermediates required by research institutions and process analytics. Its structure enables targeted derivatization, supporting high-sensitivity detection assays and niche ligand preparations, especially in environmental, clinical, and material science laboratories. Quality requirements dictate narrow impurity bands and high batch consistency.

    Industry compliance standards

    • ISO 9001 Quality Management System
    • ISO/IEC 17025 (testing labs using synthesized reagents)
    • AOAC International Methods Validation (reagents for food/environmental analysis)
    • ASTM D Testing Protocols for specialty standards

    Typical usage ratio

    • 0.2–2.5% in synthesis of complexometric titrants or derivatizing agents; scale varies from gram to kilogram depending on downstream method.

    Downstream process integration

    • Integrated as a starting substrate for multi-step functionalization and salt formation.
    • Employed in high-purity preparative lines equipped for microanalytical and spectroscopic QC.
    • Aliquots validated for reproducibility through NMR, FTIR, and ICP-OES assays.

    Final product types

    • Analytical reagent kits (e.g., transition metal indicators)
    • Chelating agent intermediates for environmental analysis
    • Reference compounds for LC–MS and GC–FID calibration
    Free Quote

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    Certification & Compliance
    More Introduction

    1,6-Naphthyridine-2-Carboxylic Acid: Insights from the Manufacturer

    A Closer Look at 1,6-Naphthyridine-2-Carboxylic Acid

    In our facility, 1,6-Naphthyridine-2-Carboxylic Acid has earned its place as a reliable building block for chemists working across pharmaceutical, agrochemical, and advanced materials research. The name may not roll off the tongue, yet its value in organic synthesis deserves recognition. Over the years, working in this industry has shown the difference between a product built for cost alone and one developed with consistency, purity, and efficiency in mind. Our team respects that researchers and manufacturers need more than a raw compound—every batch must offer predictable results, batch-to-batch, year after year.

    This product emerges from a series of meticulously controlled steps in our labs, using select starting reagents and carefully chosen catalysts. We have seen firsthand what a difference high-purity crystalline powder can make in downstream results, so we go beyond the ordinary when optimizing our crystallization and final drying stages. The specifications we achieve come from years of adjusting process variables—solvent ratios, temperature profiles, and purification techniques—to squeeze out every trace of side product, solvent residue, and moisture.

    Model and Specifications

    In our experience, the decision between one model or grade and another often comes down to the sensitivity of the intended application. Our core process produces 1,6-Naphthyridine-2-Carboxylic Acid as a white to off-white crystalline solid. Through repeated trials, our chemists have locked in a melting point and purity range that consistently meets HPLC thresholds above 99% for pharmaceutical research and labor-intensive medicinal chemistry. Moisture content stays under a strict cutoff, with Karl Fischer titration on every lot. The residual solvent profile fits compliance needs for those scaling up synthesis—no surprises there. Particle size sits in a range optimized for solubility and handling, based on feedback from university labs and process development groups we supply.

    Some customers in the past have questioned why our technical sheets avoid wide range specifications. The reality is, we tailor our analytical profiles from results, not marketing targets. Shifts in impurity profiles throughout the year, even from small changes in input material quality, lead some producers to widen their tolerances. We take the extra step of pausing for extra purification or re-blending if a batch drifts. Reliable specifications come from process discipline, not wishful thinking.

    Typical Use Cases Based on Direct Feedback

    Through direct dialogue with the people using our acid, we have learned that its core value lies in its role as a versatile intermediate. Researchers trust this molecule to anchor synthetic routes to naphthyridine backbones, which appear in kinase inhibitors, novel antibiotics, and plant-protection agents. Academic groups rely upon its carboxylic acid function for easy transformation into esters and amides, linking the naphthyridine ring to more complex molecular frameworks. Several partner labs cite its behavior under mild coupling conditions as a strength, saying it resists the stubborn side reactions that frustrate parallel synthesis.

    Sourcing managers occasionally press us on why we do not offer several “grades” at a steeply layered price scale. In reality, reproducibility counts more for end-users than cut-rate prices. Trial after trial on our line has proven that minor impurities in this acid—often undetected in cheaper products—can disrupt target reactions, causing chromatography headaches and loss of time. Our attention to specification details comes after seeing many a project’s setbacks traced to off-brand acids with undetected minor contaminants.

    Among our regular buyers, medicinal chemists appreciate that the product dissolves well in polar aprotic solvents and holds up under common amide coupling procedures without generating troublesome by-products. This means better yields, cleaner workups, and less column time. Agrochemical product developers report that its consistency allows faster progress, since every molecule in a series behaves as expected—no need to account for batch-to-batch variability or unknown reactivity quirks.

    Manufacturing Challenges and Process Learnings

    Practical knowledge from our plant shows that this acid’s route to high purity presents a series of chemical and engineering challenges. Not all commercial lots are equal—producing small quantities in flasks does not scale directly to multi-kilogram reactors. Our team spends months on process transfer, eliminating bottlenecks like incomplete cyclization, color body formation, or filter clogging. Long years in chemical manufacture have taught us that every structural analog in the naphthyridine series poses different headaches. This compound, in particular, exhibits a stubborn affinity for trace metals and can capture them from even trace-contaminated glassware or solvent.

    Avoiding these trace contaminants requires constant vigilance. Stainless steel lines and reactive vessel coatings form part of our solution, along with rigorous cleaning protocols and dedicated warehousing for input materials. Our QA staff routinely checks for ppm-level contamination that would pass unremarked in food or industrial chemical manufacture. For pharmaceutical precursors like this, there is no shortcut or substitute for hard evidence—every finished batch must prove its case, through analysis not assumption.

    Differences between 1,6-Naphthyridine-2-Carboxylic Acid and Similar Compounds

    Chemists visiting our site sometimes ask about the difference between our acid and more common naphthyridine isomers, such as 1,8-naphthyridine. On paper, small shifts in ring nitrogen positions look inconsequential, but in practice, reactivity profiles and downstream adaptability change drastically. Our experience shows that 1,6-Naphthyridine-2-Carboxylic Acid offers a unique substitution pattern, placing the carboxylic group between two ring nitrogens. This arrangement enables regioselective reactions, providing synthetic handles that differ from the 1,5-, 1,7-, or 1,8 analogs.

    Pharmaceutical partners often point out that biological testing sometimes returns drastically different profiles, even with apparently minor structural differences. Slight variations in electronic density and heterocyclic shape can make or break the binding efficiency in target screening. This compound carves out a unique space in drug discovery libraries. In contrast, other isomers fail to provide the same balance of chemical reactivity, solubility, and coupling compatibility in scaled procedures.

    We do receive requests for custom derivatives—esters, salts, or protected forms—based on the 1,6-naphthyridine core. Here is where practical knowledge counts: the parent carboxylic acid serves as an adaptable launching pad for a range of modifications, while other ring positions complicate functionalization or cheapen the final product’s synthetic value. Years of feedback confirm that trying to substitute other naphthyridine carboxylic acids in place of this one achieves few, if any, of the same successful downstream outcomes.

    Solutions for Sourcing and Production Concerns

    Our technical teams deal with common customer worries about quality drift, unpredictable lead times, and regulatory compliance. Our solution always circles back to hands-on accountability at every manufacturing stage. We choose neither to outsource key steps nor chase sketchy bulk lots overseas. The result is reliable traceability and transparency in every lot, proven by dozens of audit visits and regulatory reviews. We maintain full control from raw material intake to packaged delivery, knowing this focus guards against contamination, mislabeling, or mishandling that could undermine safety or research reliability.

    Transportation remains a stubborn challenge for sensitive chemicals. Even the best product fails if humidity or temperature spikes degrade its quality between our warehouse and a client’s bench. Over the years, we have tested multiple packaging solutions, ultimately settling on layered moisture-barrier liners and desiccant inserts to protect the acid’s structure. Our logistics staff steers clear of trans-shipment through climates notorious for cargo bay sweating or rough handling. After acting on customer suggestions, we have fine-tuned our delivery process to prioritize on-time performance and immediate cold-chain confirmation where needed.

    Research organizations and contract manufacturers sometimes worry about long-term storage, especially if they must keep extra product on-hand for regulatory filings or repeat synthesis rounds. Our published stability studies show that, stored in the original sealed packaging in a dry, cool environment, 1,6-Naphthyridine-2-Carboxylic Acid retains chemical integrity for years, not months. QA checks continue beyond shipment, tracking retained samples to ensure company-wide learning and rapid troubleshooting if complaints arise.

    Why Our Manufacturing Philosophy Matters

    Our long-standing focus on product reliability comes from direct conversations with chemists and process engineers. The high stakes in pharmaceutical R&D, crop protection, and advanced materials development do not allow the luxury of do-overs. Trial and error in the plant have made us wary of shortcuts and forced us to embrace continuous improvement. For us, manufacturing 1,6-Naphthyridine-2-Carboxylic Acid goes beyond chemical reaction; it means combining a craftsman’s mindset with the rigor of science, since every faulty lot has costs that ripple far beyond our walls.

    We designed our documentation trail to give customers a window into every production phase. Certificates of analysis provide not just numbers, but historical reference points that reveal long-term batch averages and rare outlier events. We respond to non-conformance reports with direct access to our process logs and decision rationale, not generic apologies. Our chemists work side-by-side with external partners for method development, impurity identification, and troubleshooting, treating every inquiry as a chance to improve both our product and the broader field.

    Reflections on Market Trends and Future Developments

    Market dynamics in the specialty chemical field continue to change. Supply chain shocks, regulatory revamps, and pressures around sustainability require active adaptation. In the last two years, we have migrated part of our plant energy over to renewable sources, without trade-offs in throughput or specification control. Waste minimization efforts reflect not only outside demand, but what we have learned over decades testing, scaling, and refining. As the bar for environmental compliance rises, our process engineers spend as much time on solvent capture, water treatment, and emissions reduction as they do on reaction performance.

    Several customers have asked about the possibility of green chemistry alternatives for the production of 1,6-Naphthyridine-2-Carboxylic Acid. Through reaction optimization, solvent swaps, and improved work-up protocols, we cut process mass intensity for each lot delivered. Our documentation captures this progression, targeting both transparency and real gains for clients managing their own sustainability reports.

    Continuous Dialogue with the End Users

    A culture of honest feedback and continuous improvement drives much of how we operate. It is common for our senior development chemists to spend hours in the field each month, investigating subtle issues in analytical performance or end-use reliability. Customers call us for everything from reaction troubleshooting to custom method development, and we answer with direct access to the people who built the process line. Challenges in this sector keep evolving, but after years of hard work, we have learned the answers depend on both. Listening closely and responding decisively, our team sees every lot shipped as a test of our commitment.

    As the global research community tackles new therapeutic molecules and advanced materials, a dependable source for 1,6-Naphthyridine-2-Carboxylic Acid forms one small, but essential, piece in the puzzle. Experience in chemical manufacturing has proven that shortcuts in specification, handling, or communication lead to setbacks. For us, each order presents a chance to reaffirm our values—clarity, diligence, and respect for the scientific work made possible by reliable building blocks. Years in the field have taught us that true partnership means not only supplying high-purity acid, but earning the trust that comes from facing challenges together.