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1H-Indazole-4-Carboxylic Acid

    • Product Name 1H-Indazole-4-Carboxylic Acid
    • Alias 4-Indazolecarboxylic acid
    • Einecs 629-699-5
    • 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
    VTB
    Specifications

    HS Code

    267322

    Product Name 1H-Indazole-4-Carboxylic Acid
    Cas Number 1072-98-6
    Molecular Formula C8H6N2O2
    Molecular Weight 162.15 g/mol
    Appearance White to off-white solid
    Melting Point 235-238°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water, soluble in organic solvents
    Smiles C1=CC2=C(C=CN2)C(=O)O1
    Inchi InChI=1S/C8H6N2O2/c11-8(12)6-3-1-2-5-7(6)9-10-5/h1-3H,(H,11,12)(H,9,10)
    Storage Conditions Store at room temperature, in a tightly closed container
    Ec Number 213-997-5

    As an accredited 1H-Indazole-4-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque screw-cap bottle containing 25 grams of 1H-Indazole-4-Carboxylic Acid; clearly labeled with chemical name, quantity, and hazard warnings.
    Shipping **Shipping for 1H-Indazole-4-Carboxylic Acid:** The chemical is securely packaged in sealed, chemical-resistant containers and labeled according to regulatory requirements. It is shipped promptly via trusted carriers with appropriate documentation, ensuring compliance with safety and handling standards. Temperature and moisture control measures are observed to maintain compound integrity during transit.
    Storage 1H-Indazole-4-carboxylic acid should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as oxidizers. Keep the container clearly labeled and stored at room temperature. Prevent moisture ingress and avoid excessive heat. Handle using appropriate personal protective equipment to minimize exposure risks.
    Application of 1H-Indazole-4-Carboxylic Acid

    Applications of 1H-Indazole-4-Carboxylic Acid in Industrial Manufacturing

    As the direct manufacturer of 1H-Indazole-4-Carboxylic Acid, we supply this specialty intermediate to a select group of advanced sectors, where its unique molecular structure supports synthesis routes for high value-added downstream applications. We support downstream operations by providing traceable quality control, regulatory documentation, and in-depth technical expertise for every industrial integration scenario described below.

    1. Pharmaceutical Intermediates for Anti-inflammatory Drugs

    Our facility produces 1H-Indazole-4-Carboxylic Acid to pharmaceutical companies developing active pharmaceutical ingredients (APIs) for non-steroidal anti-inflammatory drugs (NSAIDs). Process engineers incorporate the acid in sequential heterocycle-building steps, targeting indazole scaffolds known for their biological activity. Our raw material enters synthesis routes strictly controlled under international pharmacopeial standards, and the downstream transformation utilizes streamlined amide coupling to construct the core structure of commercial anti-inflammatory agents.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA CFR Title 21 Parts 210/211
    • EU GMP Part II for API production
    • Ph. Eur. and USP monographs for process chemicals (where applicable)

    Typical usage ratio

    • 0.6–1.5 molar equivalents per batch, adjusted based on the optimization of indazole ring formation and impurity control strategies

    Downstream process integration

    • Introduced during the cyclocondensation step as the indazole ring precursor, followed by transformation through acylation and functionalization in semi-continuous or batch reactors

    Final product types

    • API intermediates for NSAIDs such as indazole derivatives
    • Finished tablet and injectable anti-inflammatory pharmaceuticals after subsequent downstream formulation

    2. Synthesis of Agrochemical Active Ingredients

    Technical teams at crop protection companies use our material as a key intermediate to build indazole-core structures in the development of selective fungicides and growth regulators. The acid group enables facile coupling and further derivatization under mild process conditions, allowing precise control of bioactive moieties in the final agrochemicals. Precise batch traceability supports regulatory submissions and stewardship audits in target markets.

    Industry compliance standards

    • ISO 9001:2015 for chemical manufacturing
    • FAO/WHO JMPR guidance on technical raw materials
    • REACH pre-registration for EU shipments
    • China ICAMA certification for export-bound intermediates

    Typical usage ratio

    • 7–14% by weight in final technical active ingredient synthesis batches; stoichiometry varies by target molecule and downstream substitution pattern design

    Downstream process integration

    • Serves as the initial indazole scaffold in multi-step coupling and alkylation processes, entering the reactor during the first heterocycle assembly phase and purifying under solvent-controlled crystallization steps

    Final product types

    • Technical-grade fungicide and plant regulator active ingredients containing indazole backbones
    • Formulated agrochemicals for crop protection, such as granules and emulsifiable concentrates

    3. Advanced Dye and Pigment Manufacturing

    Specialty dye manufacturers select our indazole derivative for the controlled synthesis of colorant intermediates in high-temperature-resistant dye formulations for fibers, plastics, and coatings. The carboxylic acid moiety enables integration via diazonium coupling or condensation with aromatic amines, delivering the required stability and chromophore intensity. Rigorous supply documentation supports compliance with environmental and workplace safety regulations relevant to pigment processing.

    Industry compliance standards

    • OEKO-TEX® Standard 100 chemical restrictions for textile raw materials
    • REACH Annex XVII on azo dyes (restricted substances assessment)
    • ISO 9001 and 14001 for chemical processing and environmental controls
    • Global Textile Standard (GOTS) requirements for dye precursors (where applicable)

    Typical usage ratio

    • 0.5–2.0% by dry product mass, calculated based on target color index and final product concentration requirements

    Downstream process integration

    • Blended during the initial pigment base formation, followed by diazo coupling with aromatic amines and subsequent purification by precipitation or filtration

    Final product types

    • Synthetic azo and heterocyclic dye intermediates
    • High-purity textile dyes for polyester, nylon, and acetate fibers
    • Color masterbatches for polymer processing

    4. Development of Novel Heterocyclic Research Compounds

    Contract research organizations (CROs) and custom synthesis labs regularly procure our material for exploratory and pilot programs targeting novel heteroaromatic compounds. Its defined purity and lot-to-lot consistency support synthesis of experimental small molecules, tools for medicinal chemistry SAR studies, and ligand scaffolds in screening assays. Researchers rely on our quality control protocols and batch documentation to maintain reproducibility and facilitate compliance with institutional review and granting body audits.

    Industry compliance standards

    • ISO/IEC 17025 laboratory accreditation (where applicable)
    • Standard Operating Procedure (SOP) alignment under institutional regulatory review
    • Material traceability requirements by major pharmaceutical and biotechnical consortia

    Typical usage ratio

    • Variable from 0.1–10 mmol scale per reaction, adjusted at the bench by researchers according to synthetic route and library diversity objectives

    Downstream process integration

    • Dosed at the building block stage for library synthesis or lead optimization, entering amidation, Suzuki coupling, or directed ortho-metalation processes in custom batch or parallel synthesis setups

    Final product types

    • Discovery-phase heterocyclic libraries
    • Screening compounds for medicinal chemistry programs
    • Reference standards for analytical R&D use

    5. Synthesis of Specialty Electronic Materials

    Manufacturers of advanced organic semiconductors incorporate this compound as an indazole-based electron-transport unit into the backbone of organic light-emitting diodes (OLEDs) and photovoltaic materials. The carboxylic functionality supports post-functionalization for integration into multicomponent molecular architectures. Quality assurance relies on consistency in particle size and minimal ionic impurities, allowing reproducible thin-film formation and device fabrication under cleanroom protocols.

    Industry compliance standards

    • ISO 14001 for safe handling and environmental controls in electronics chemicals
    • RoHS Directive compliance for electronic material precursors
    • TÜV Rheinland safety audits for specialty chemical suppliers
    • REACH notification for European device manufacturing

    Typical usage ratio

    • 0.2–1% by mass as a monomeric building block, calculated according to device design and molecular weight specifications

    Downstream process integration

    • Added to solution-phase polymerization or cross coupling stages, subsequently purified and isolated before deposition into thin-film layers by spin-coating or vapor phase methods

    Final product types

    • Electron-transporting materials for OLED displays
    • Indazole-based small molecule OLED emitters
    • Donor-acceptor polymers for organic electronics
    Free Quote

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    Certification & Compliance
    More Introduction

    Unlocking Chemistries with 1H-Indazole-4-Carboxylic Acid: A Manufacturer’s Perspective

    Introduction: Quality Rooted in Hands-On Production

    Producing 1H-Indazole-4-Carboxylic Acid from our own facility has kept us close to both the molecular backbone and the partners who rely on it. The compound, with the chemical structure of C8H6N2O2 and a precise molecular weight of 162.15 g/mol, enters our reactors day after day. With over a decade spent optimizing our synthesis routes, our technicians and chemists prefer to look beyond specs and certificates. Instead, we address the real-life demands and persistent frustrations faced by downstream enterprises—whether in pharmaceuticals, agrochemicals, or material science.

    Consistent Quality Starts at the Reactor

    Each production campaign begins with thoroughly sourced starting materials. Years of trial and learning have taught us that cheap, impure raw supplies bring more headaches than savings. Continuous process monitoring and batch-to-batch checks strengthen our confidence when sending 1H-Indazole-4-Carboxylic Acid out the factory gate. Reliable purity—often ≥98% by HPLC—comes not from magic but from steady verification and a refusal to cut corners. Stability as a pale solid, easily handled in drums and bottles, matters for downstream reproducibility. Grit from decades on the floor keeps us alert; we know that a slippage in even a minor step can echo all the way through partners’ synthetic schemes.

    Refining Particle Size and Handling for Seamless Integration

    With 1H-Indazole-4-Carboxylic Acid, one type never fits all applications. Tablets, fine chemicals, and intermediates—each demands a preferred texture. Some customers run chromatography, seeking dust-free, free-flowing powder that won’t bridge a hopper or clog a filter. Others need material fit for milling or direct compounding. From our side, custom sieving and the use of dedicated mills deliver batches in the particle ranges defined by real-life needs, not marketing gloss. This matches tightly held R&D habits and manufacturing practices that won’t tolerate second-rate handling.

    Why Structural Consistency Beats Commodity Thinking

    Our technical team takes special responsibility for batch reproducibility. In certain fields, one-off oddities can spell disaster, especially in pharmaceutical discovery or materials research. 1H-Indazole-4-Carboxylic Acid serves as a functional building block for APIs and specialty chemistries due to its functional carboxylic acid at position 4, which opens routes to amides, esters, or even heterocyclic expansions. Contrast this with general indazoles or carboxylates scattered at different ring positions—the substitution pattern changes everything, from reactivity to final product biological profile. In our experience, project yields and regulatory hurdles force developers to scrutinize every single variant. We help by marking and segregating lots by detailed NMR and LC/MS profiling, always ruling out the kind of mix-ups that could sink months of pipeline work.

    Documented Traceability: Not Just a Paper Exercise

    Traceability in chemical manufacture only works if documentation matches real chemical events. Rubber-stamping a batch sheet never saved a partner from a regulatory audit or process deviation. Every pack of 1H-Indazole-4-Carboxylic Acid that rolls out comes backed by a full trail of raw lot, processing logs, and QC signatures. Our certificates include method specifics and impurity footprints, offering a reliable bridge if a downstream procedure develops an unexpected hitch. We view this as a fundamental promise—a pact based on shared technical risk, not just a checkbox for compliance.

    Addressing Challenges Unique to Indazole Chemistry

    Over the years, several obstacles set 1H-Indazole-4-Carboxylic Acid apart from generic heterocycles or benzoic acid variants. The indazole core, featuring nitrogen at adjacent 1 and 2 positions, can prompt ring-opening side reactions or undesired oxidation if the process gets sloppy. Early on, our labs caught this risk by tightening our solvent and temperature tolerances and switching to inline analytical controls. We’ve faced pressure to cheapen steps and ease up on storage standards, especially when pushes come from volatile markets. But those cuts show up in lower assay values or hidden traces of unstable byproducts—troublesome for anyone running scale-ups or moving to GMP synthesis.

    Meet Stringent Demands in Regulated Sectors

    Parties involved in regulated drug development or high-value crop protection do not accept unexplained deviation or uncertain sourcing. In these sectors, 1H-Indazole-4-Carboxylic Acid directly supports synthetic efforts for kinase inhibitors, neuraminidase antagonists, and other complex molecules. A single off-flavor in NMR spectra can flag a new impurity, forcing repeated work at both our plant and partner labs. We communicate early and often about minor and major changes, whether in storage, handling, or specification shifts after customer inquiry. This transparency leads to mutual trust—vital when a delayed batch spells missed clinical milestones.

    Comparing with Other Indazole and Aromatic Carboxylic Acids

    From a producer’s vantage, not all “carboxylic acid” indazoles behave the same. The position of the acid dramatically alters solubility and downstream derivatization. For example, 3-carboxylic acids offer different conjugation chemistry. Our 4-carboxylic acid model gives superior stability during amidations and can handle more rigorous temperature swings in larger reactors. As for other indazole analogs, such as halogenated or methylated versions, 1H-Indazole-4-Carboxylic Acid offers a clean starting point with lower natural background impurities. Decades of customer feedback have made clear that such subtle points greatly matter for reproducibility, both in academic research and industrial process development.

    Supporting Customization: Batches That Respect Unique End-Use

    Requests for custom synthesis or altered specifications arrive often. We’ve seen projects in the past grind to a halt because a standard grade just wasn’t fit for an intended coupling or crystallization. Our flexible approach started as a way to handle these unexpected asks. Whether that means tailoring batch sizes—from pilot grams to tens of kilos—or locking in a tighter chloride spec for sensitive pharmaceutical partners, our production lines adapt without drawing out lead times or inflating costs.

    Environmental Responsibility Anchors Manufacturing

    The indazole core can be tough to synthesize cleanly if waste isn’t managed. Over the years, regulations and our own ethical drive have prompted us to install solvent recovery, invest in effluent treatment, and work closer with suppliers to reduce upstream contamination. On the floor, our team actively monitors emissions and seeks ever-safer alternatives for intermediate reagents. Though such shifts add complexity and retraining, we view this as the cost of continued operation in a world moving toward more sustainable chemistry.

    Troubleshooting Downstream Processes with Partners

    Chemical supply does not end with handing over a package. Many teams run into sticking points during scale-up, tabletization, or subsequent coupling steps. Our technical support team includes both experienced process chemists and line operators who’ve handled indazole intermediates hundreds of times. We respond to something as simple as minor solubility changes—often rooted in unnoticed humidity fluctuation at filling—or as complex as persistent side products during acylation. Our observations have shown that simple tweaks, like adjusting loading sequence or predrying protocols, solve many problems before costly delays start piling up.

    Addressing Analytical and Purity Standards Beyond the Certificate

    Not all customers stop at a standard COA. Some need full LC-MS spectra, chiral resolution data, or bespoke impurity mapping along with AAS details for metal content. Over years, we built up an in-house QC lab with a battery of modern instruments, covering both targeted and exploratory analyses. We run parallel tests for moisture, heavy metals, and residual solvents, since each project and regulatory pathway demands its own slice of the data. Our results feed back into production adjustments, so each campaign reflects what’s genuinely needed, not just what’s cheapest or quickest.

    Enhancing Process Flow and Minimizing Downtime

    The manufacture of 1H-Indazole-4-Carboxylic Acid calls for nimble logistics. Experience tells us that a stalled delivery or a container with caked solid stirs up delays in the next operation downstream—sometimes costing more labor and raw input than the original error. We keep stocks in climate-controlled stores, rotate inventory with a strict FIFO policy, and design our packaging to withstand long-haul transport and customs checks. Each drum or bottle is labeled with expiry and suggested storage details based on real-world shelf life studies, aiming to prevent those surges of uncertainty that put timelines at risk.

    Partnering in Research and Development

    The best ideas spring up where chemists can count on consistent, traceable inputs. We have worked closely with university labs, startup biotech, and established pharmaceutical concerns bringing new scaffolds to human or veterinary medicine. Our technical exchanges have supported troubleshooting beyond ingredient provision—for example, advising on the best coupling reagents or protection strategies for the indazole carboxyl, based on hard-earned experience from previous production runs.

    Safer Storage and App Handling Recommendations

    Safe, controlled storage ensures 1H-Indazole-4-Carboxylic Acid keeps its intended properties and does not develop unwanted reactivity. While we do not substitute for professional safety documentation, practical company knowledge counts just as much at warehouse and bench scale. Keep product cool, dry, and in a well-ventilated space. Reseal containers promptly after sampling or dispensing, and avoid cross-contamination with incompatible solvents and acids. These habits sound simple, but over time, such discipline prevents many headaches and upholds the standards we and our partners value.

    Sustaining Technical Dialogue

    Customers, be they formulation chemists or process engineers, often approach with their own ideas on how to push boundaries using the 1H-Indazole-4-Carboxylic Acid scaffold. Good manufacture means not just delivering an item, but also sharing lessons. Sometimes these lessons arose from troubleshooting difficult side reactions, or even discovering unexpected downstream applications in catalysis and advanced material research. Our role has always blended manufacturing with honest feedback: We clarify limitations, flag regulatory gray areas, and jointly solve process snags when they arise.

    Learning from Past Mistakes and Process Failures

    The road to present quality featured plenty of stumbles early on—from missed drying steps to failed crystallizations triggered by over-concentrated mother liquors. Rather than hide behind opaque processes, we documented and corrected every misstep, improving both protocols and staff training. This openness to learning has taught us that even a widely used intermediate like 1H-Indazole-4-Carboxylic Acid only survives in the marketplace by earning trust, campaign after campaign. It has also given us a better understanding of what matters to real chemists at the bench and on the pilot plant floor.

    Positioning for Future Synthesis and Regulatory Shifts

    Markets for heterocyclic building blocks shift as new synthetic pathways and targeted medicines gain ground. We follow these trends, tuning our process recipes to accommodate greener chemistry when practical. Upgrades might mean swapping in less hazardous dehydrating agents or reducing waste through improved yield and recovery. Compliance now includes not just regional standards, but also ever-stricter multinational norms—so we constantly audit not only our own process, but also those of upstream suppliers, ensuring every gram meets higher bar.

    Comparing to Market Alternatives and Common Pitfalls

    Suppliers of indazole-based products abound, but users find that price alone tells little about end use suitability. We have acquired known lots of competing materials over the years to benchmark for purity, solubility, and reactivity. Inferior lots, often traced back to lax process control, can leave unpredictable residues or variation in solid state—turning what begins as a routine synthesis into a troubleshooting marathon. By maintaining direct control over all process steps, we cut out the ambiguity that too often accompanies resold or lightly repackaged product streams.

    Continuous Improvement Rooted in Factory Experience

    Fielding constant feedback and probing customer returns, we invest in continuous renewal—whether that means swapping out a problematic reactor gasket material, refitting driers, or adapting staff instructions after a close call. We draw on the collective wisdom of every operator and chemist who passes through our doors, and we constantly share this practical knowledge with current and future partners.

    Conclusion: Building Confidence Batch by Batch

    Supplying 1H-Indazole-4-Carboxylic Acid means placing a promise behind every container. We recognize that no amount of paperwork or digital tracking replaces direct, factory-born knowledge of the challenges, opportunities, and details that shape each production campaign. Everything we know about its synthesis, QA/QC, regulatory context, and technical support reflects thousands of hours on the shop floor and in partner discussions. As the field for heterocyclic intermediates expands, our willingness to improve, share, and listen stands as our primary advantage. We welcome questions, shared learning, and new collaborations on every shipment, drawing on solid roots in production and chemistry to support customers who demand assurances that paperwork alone can’t offer.