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8-Hydroxyquinoline-2-Carboxylic Acid

    • Product Name 8-Hydroxyquinoline-2-Carboxylic Acid
    • Alias 8-Hydroxy-2-quinolinecarboxylic acid
    • Einecs 242-924-4
    • 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

    748708

    Chemical Name 8-Hydroxyquinoline-2-Carboxylic Acid
    Cas Number 134-31-6
    Molecular Formula C10H7NO3
    Molecular Weight 189.17 g/mol
    Appearance Pale yellow crystalline powder
    Melting Point 237-240 °C
    Solubility In Water Slightly soluble
    Boiling Point Decomposes
    Iupac Name 8-hydroxyquinoline-2-carboxylic acid
    Synonyms Kynurine, Oxine-2-carboxylic acid
    Storage Conditions Store at room temperature, in a dry place
    Pubchem Cid 14593

    As an accredited 8-Hydroxyquinoline-2-Carboxylic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 8-Hydroxyquinoline-2-Carboxylic Acid, 25g, comes in a sealed amber glass bottle with a tamper-evident cap and chemical hazard labeling.
    Shipping 8-Hydroxyquinoline-2-carboxylic acid is shipped in tightly sealed containers to prevent moisture absorption and contamination. The chemical is handled according to standard hazardous material regulations, often with appropriate labeling. It should be transported at ambient temperature, away from incompatible substances, with adherence to local and international shipping guidelines for laboratory chemicals.
    Storage Store 8-Hydroxyquinoline-2-Carboxylic Acid in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep in a cool, dry, and well-ventilated area, preferably in a chemical storage cabinet. Avoid contact with oxidizing agents and strong bases. Label containers clearly, and ensure access is restricted to trained personnel following standard laboratory safety protocols.
    Application of 8-Hydroxyquinoline-2-Carboxylic Acid

    Applications of 8-Hydroxyquinoline-2-Carboxylic Acid in Industrial Manufacturing

    8-Hydroxyquinoline-2-carboxylic acid plays a specialized role in multiple regulated chemical sectors, supporting advanced performance in formulation and downstream integration. As a direct manufacturer, we detail its precise use-cases across key industries where this material consistently meets process requirements and compliance benchmarks.

    1. High-Performance Metal Ion Chelation in Analytical Reagents

    Laboratories and specialty reagent manufacturers employ 8-hydroxyquinoline-2-carboxylic acid as a metal ion scavenger in trace metal analysis kits, where accurate detection depends on consistent chelating activity, low background interference, and batch traceability. Its integration is aligned with chromatographic purity and heavy metal quantification routines, especially in spectrophotometric and colorimetric assays for water quality and food safety matrices.

    Industry compliance standards

    • ISO 17034:2016 Reference Material Producers
    • ISO/IEC 17025:2017 Testing Laboratories
    • APHA Standard Methods for the Examination of Water and Wastewater
    • AOAC International Guidelines for Analytical Methods

    Typical usage ratio

    • Concentration varies from 0.01% to 0.2% w/v (100–2,000 ppm), adjusted in formulation to match target metal ion load and desired sensitivity in each analytical matrix.

    Downstream process integration

    • Dissolve as an aqueous or buffer solution component; integrate post-buffer adjustment, before reagent bottling or kit assembly, ensuring standardized chelation reactivity in the final reagent set.

    Final product types

    • Trace metal test kits
    • Colorimetric water analysis reagents
    • Reference and calibration solutions for metal quantitation
    • Ready-to-use chelation buffers for lab QC protocols

    2. Complexing Agent in Electroplating and Metal Surface Treatment

    Industrial metal finishers leverage the complexation properties of 8-hydroxyquinoline-2-carboxylic acid to stabilize plating baths for copper, nickel, and zinc processes. It supports deposition uniformity and suppresses unwanted side reactions during high-precision component surface treatment, with dosing aligned to specific line chemistry and compliance monitoring for discharge regulations.

    Industry compliance standards

    • ASTM B700 Standard Guide for Electrodeposited Coatings of Silver for Engineering Use
    • ISO 9001:2015 Quality Management Systems (for process control)
    • REACH Regulation (EC) No 1907/2006 for chemical management
    • RoHS Directive 2011/65/EU for plated components in electronics

    Typical usage ratio

    • Doses typically range from 50 ppm to 500 ppm in plating baths, adjusted based on target deposition rate, bath turnover, and metal ion concentration. Optimization follows routine bath analysis and titration results.

    Downstream process integration

    • Added directly to the plating bath during make-up and as periodic maintenance, either manually or via automated dosing, after pH adjustment and before initiation of electrolytic deposition cycles.

    Final product types

    • Electroplated electronic connectors
    • Decorative plated components for automotive assemblies
    • Precision instrument housings
    • Engineered hardware for aerospace equipment

    3. Intermediary for Specialty Pharmaceutical Ingredients

    In pharmaceutical synthesis, 8-hydroxyquinoline-2-carboxylic acid functions as a tailored intermediate, especially in the construction of complex heterocyclic scaffolds and metal chelate drugs. It enters regulated processing environments subject to GMP oversight, where its purity profile and low residual metal content contribute to repeatable yield and consistent quality of advanced active pharmaceutical ingredients (APIs).

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for API intermediates
    • USP <795> and <797> Compounding Standards (if used in extemporaneous production)
    • 21 CFR Part 211 U.S. cGMP for finished pharmaceuticals

    Typical usage ratio

    • Used stoichiometrically relative to target intermediate formation, typically 0.5–1.5 equivalents in single- or multistep synthesis, with process engineers adjusting charge based on conversion and impurity profiles.

    Downstream process integration

    • Charged to reaction vessels at designated stages following initial solvent charging; monitored for residual content in downstream purification steps to comply with API impurity specifications.

    Final product types

    • Advanced pharmaceutical intermediates
    • Specialty chelate drugs for diagnostic imaging
    • Metal-based anti-infective agents
    • Regulated drug substance building blocks

    4. Stabilizer and Pigment Modifier in Technical Dye Manufacture

    Technical dye and pigment producers rely on 8-hydroxyquinoline-2-carboxylic acid as a metal-binding modifier to enhance color stability and lightfastness. Its precise introduction during dye synthesis or post-treatment affects hue, particle fineness, and suspension properties, especially where the final pigments must meet product-specific environmental and textile standards.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile chemical safety
    • EN 71-3 Safety of Toys: Migration of Certain Elements (for colored plastics)
    • GMP Regulation (EC) No 2023/2006 for food contact colors
    • ISO 9001:2015 Quality Management Systems (for dye/pigment QC)

    Typical usage ratio

    • Dosing ranges from 0.2% to 2% w/w relative to the dye or pigment batch, with application trials determining the minimum effective concentration for each substrate to achieve target color strength and stability.

    Downstream process integration

    • Injected during pigment slurry milling or into the dye solution after primary synthesis; precise control through in-process sampling and colorimetric measurement prior to final blending, drying, or spray conversion.

    Final product types

    • Organic and inorganic textile dyes
    • Colored masterbatch concentrates
    • UV-stable pigments for plastics, paints, and coatings
    • Technical inks for industrial labeling

    5. Component in Corrosion Inhibition Formulas for Industrial Water Treatment

    Manufacturers of closed-loop and open recirculating water treatment systems incorporate 8-hydroxyquinoline-2-carboxylic acid as a selective chelating agent within anti-corrosion blends. It targets transition metal ions that accelerate pitting, improving system longevity while supporting regulatory compliance for water release and occupational safety.

    Industry compliance standards

    • ANSI/ASHRAE Standard 188-2018 (Legionellosis: Risk Management for Building Water Systems)
    • USEPA National Primary Drinking Water Regulations (where applicable in facility discharge)
    • EN 12123-1999 Chemicals used for treatment of water intended for human consumption
    • ISO 14001:2015 Environmental Management Systems

    Typical usage ratio

    • Blend inclusion usually between 1–10 ppm in treated water; dosage fine-tuned based on real-time monitoring of water chemistry, system metallurgy, and operational turnover rates.

    Downstream process integration

    • Premixed with other corrosion inhibitors and antiscalants at the chemical feed station; gradual dosing into system circulatory tanks or pipelines based on continuous sensor feedback and compliance sampling routines.

    Final product types

    • Industrial water circuit corrosion inhibitor fluids
    • Power plant water treatment additives
    • HVAC closed-loop chemical blends
    • Factory process water maintenance agents
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    Certification & Compliance
    More Introduction

    8-Hydroxyquinoline-2-Carboxylic Acid: An Insider’s Perspective from the Production Line

    Every chemical has its rhythm in the factory. Some pour bright and clear, some need a steady hand and patience to coax from reactor to drum. Among our batch list, 8-Hydroxyquinoline-2-Carboxylic Acid stands out for its reliability and the difference careful manufacturing can make. Produced here in our plant, it balances the time-tested backbone of quinoline derivatives with a highly functional carboxylic acid group, and the end product gives you a trusted tool across research, pharmaceuticals, and specialty materials.

    Inside the Drum: What We Make and How We Make It Matter

    8-Hydroxyquinoline-2-Carboxylic Acid, in crystalline powder form, enters the workflow not as an afterthought or byproduct, but as a carefully monitored result of targeted synthesis. We work in kilo and multikilo batches, using raw inputs with confirmed origins and running every cycle with the same oversight we would expect for a mission-critical product. Purity levels frequently test above 99 percent — not because someone asked us to hit a target, but because we know off-colors or water traces will leave downstream users troubleshooting in the lab instead of working. The real difference isn’t on a paper certificate, but in hour-by-hour process control, old-fashioned familiarity with how the reaction should look and smell, and an insistence on measuring twice and packing once. Moisture content gets controlled because some customers store material for months, others weigh it right into a hot solvent, and we know both results matter.

    Model and Physical Properties: Why This Acid Stands Alone

    The standard model manufactured here follows the molecular formula C10H7NO3, creating a profile that fits both coordination chemistry and organic syntheses. Visual cues include pale-to-off-white crystalline solid, with a melting point that often confirms good product — typically between 256 and 260 °C under our process, which is itself a reliable signal that the purification went as planned. Our batches avoid excessive fines and clumping, leveraging agitation and controlled precipitation rather than shortcutting with over-drying or aggressive grinding. Bulk density follows naturally, without needing post-processing, which customers in solid-state applications recognize as a sign we aren’t pushing yield at the expense of usability. Storage stability draws on carefully sealed drums, packaging lined by material tested for migration — so you don’t get surprises from leached plasticizers or absorbed moisture mid-way through an experiment or process.

    How Customers Use It: Voices from the Field Come Back to Us

    Feedback shapes what we do. On the pharmaceutical side, a core use is as a chelating agent, exploiting the dual donor nature of the hydroxy and carboxyl groups — coordinating with metals for both therapeutic compounds and research applications in biochemistry. We’ve learned a lot from conversations with formulation chemists who emphasize consistency batch-to-batch, as even small shifts in impurity profiles can affect screening results or need extra purification downstream.
    Plant pathologists and agrochemical developers explore it for its broad biological activity, especially as a lead structure or building block in active agents. The molecule’s stability in a variety of solvents means they can run exploratory reactions without worrying about decomposition spikes above ambient temperature. Materials scientists order it for use in functional coatings, corrosion inhibitors, and fluorescent compounds. We keep hearing how sharp, clean crystallinity makes it easier to weigh, and how quick dissolution in typical solvents like methanol or DMSO means less time spent prepping and more time running core reactions.

    Distinct from the Usual 8-Hydroxyquinoline — and What That Means

    Questions often come in about what separates this acid from basic 8-hydroxyquinoline or similar derivatives. The added carboxylic group at the 2-position transforms the molecule’s behavior, widening its solubility profile and opening doors in areas the parent structure cannot reach. As manufacturers, we see this play out both in synthesis and in end use. The acid’s extra polarity changes how it complexes metals, giving tighter, often more selective chelation — a property that matters a great deal in catalysis or analytical protocols where bleed-through or competing ligands are a headache.
    Most substitution patterns on quinolines require multi-step, lower-yield routes. The carboxylic acid process, developed and refined here, maintains both functional group integrity and overall yield. Our technical team references real-world runs instead of theoretical claims. In a side-by-side with plain 8-hydroxyquinoline, the acid-punch structure grants stronger water dispersibility and typically a more pronounced effect in bioassay screens, justifying its higher cost to quality-driven end users.

    Facing the Real Challenges in Manufacturing

    No industrial synthesis comes without headaches. The particular challenge in 8-hydroxyquinoline-2-carboxylic acid lies in managing regioselectivity during the carboxylation step. It takes careful temperature ramping and reagent addition rates to consistently hit the 2-position, as off-target substitution drops yield and complicates purification. Decades ago, these process quirks bothered us, with more off-spec material and higher loss. Over years and revisions, process engineers mapped out tighter reaction windows and implemented chromatography checks, reducing the number of problem batches. We check for minute amounts of isomers and side reaction products, using both classic chromatography and modern HPLC methods.
    Operational challenges also pop up in scale-up. Lab routes often don’t simply double into plant scale, so transition required us to adjust mixing, change the order of reagent addition, and build new monitoring set-ups. We keep an eye on waste minimization, running recapture systems wherever practical — not just for cost reasons, but because we’re always answering regulators and internal teams about greener manufacturing footprints. Not every idea pans out, but incremental improvements over time have made us more efficient than routes using higher temperatures or more exotic solvents.

    Purity, Trace Residues, and Why the Details Matter

    We’ve seen what small impurities do to both research and production. Complexes form unpredictably, spots appear during chromatography, and nobody is happy if a whole batch of a customer’s product gets tied up until a contaminant is identified. This is why we opt for additional analytical runs, not out of paranoia, but from learned experience. FTIR, nuclear magnetic resonance, and elemental analysis all play daily roles in monitoring product quality here.
    End users across the pharmaceutical, electronics, and advanced manufacturing fields sometimes request custom screens for halides or organic trace metals, and we’ve learned to support those needs rather than treat them as outliers. Some customers provide their own test methods, and we run those in parallel with our in-house standards to ensure alignment. By maintaining an open line for such collaborations, we catch small discrepancies before they launch into wider problems down the line. We never mind sharing run histories or opening up production records for technical audits — the more eyes on the process, the higher the collective standard becomes.

    Packaging Realities: Small Details, Big Results

    We pack according to need. Our most common orders range from 1 kg up to 25 kg, shipped in HDPE drums triple-lined with inert film, each batch sealed with tamper-evident bands. Repackaging for research labs takes more time and care than freight forwarding to bulk buyers, so we assign experienced handlers to small-volume lots. We mark lot codes by hand so any hint of dusting or clumping during transfer can be tracked and addressed before it ever approaches your shelves. This avoids the issues that come up with old product pulled out of cold storage and helps the user side maintain good records for traceability.
    Feedback on packaging sometimes highlights more about the product than any sales pitch. Researchers tell us that powders come out free flowing and don’t stick in spatulas — proof to us that we’re managing particle size. The kind of packaging we use also guards the acid against excessive humidity uptake, allowing the last gram in a package to behave as well as the first. The cost to us: a few extra minutes and a bit more QA, but this is better than solving usability issues after shipment.

    Handling and Safety — Knowledge Earned from Experience

    Following safe handling doesn’t earn headlines, but within a real production environment, it matters. Our teams understand the risks of handling fine organic powders, so we focus on process enclosure and effective dust control. Vent streams pass through abatement and particulate filters, storage rooms run under low ambient humidity to prevent product caking or airborne contamination. Worker familiarity allows us to spot leaks, spills, or cross contamination earlier, and process safety sheets are consulted by everyone, not just the QA staff. We encourage customer feedback in this arena because every site, lab, or production line interacts with chemicals differently and issues sometimes surface only under unique conditions.
    Some clients mention the pyrophoric potential of certain metal complexes. Our own technicians have seen the temperature sensitivity after long-term storage, so we add cooling breaks during high-temperature processes and reinforce no-smoking, anti-static, and PPE rules in our handling zones. Each of these small changes came not because regulation forced us, but because we saw the result of near-misses and minor incidents in the past. Shared knowledge with manufacturing partners and end users sharpens our approach each year.

    Applications in Academia and Industry

    Academic labs often order our 8-hydroxyquinoline-2-carboxylic acid for use in metal ion assays, pH probes, or as synthetic handles for advanced functional group transformations. Professors have shared their experiences comparing our batches to larger multinational sources, appreciating the batch-specific data and the absence of batch-to-batch variation.
    Within industry, use has broadened. One long-standing user employs it as a critical intermediate in small-molecule pharmaceutical synthesis, choosing our product largely because of low trace metal content that might otherwise derail an API route. In materials research, another group adopted our acid for its chelation-driven alteration of sol-gel properties — reporting better stability and uniform results, which they traced back to crystalline integrity and careful pH control during the synthesis. A few environmental labs have leveraged its strong chelating nature for trace heavy metal detection, using the product both as a reactive agent and as a calibration standard for instrument systems.
    We track these stories internally, not to take credit but to learn, adapt, and refine our process over time. No chemical moves in isolation; every drum we ship connects us to new advances and, sometimes, new requirements that shape the broader production flow. We have expanded our quality and logistics operations to match these evolving applications, keeping fit with both academic and industrial partners.

    Regulatory and Environmental Commitments

    The regulatory landscape never stays still. Years ago, changing rules about residual solvents and trace contaminants led us to shift our process — not reluctantly, but with the realization that adoption of greener practices made our team’s job safer and output more competitive. We monitor for REACH, TSCA, and local compliance as part of regular production auditing, even for materials moving to non-restricted markets. This commitment means changing solvents, exploring alternative washing protocols, and investing in improved waste processing, which shows real results in reduced load on effluent treatment and lower non-compliant batch rates.
    Internally, the drive for more sustainable practices led us to invest in reclaiming solvents wherever possible and reducing single-use packaging. Feedback from environmentally focused buyers prompted us to minimize outer packaging and switch to recyclable shipping materials. These changes save cost over time, but more importantly, demonstrate ongoing responsibility in manufacture — a standard we hold for ourselves regardless of external pressures.

    Differences That Customers Recognize

    Customers regularly tell us they notice the way our acid dissolves more cleanly, the color difference compared to competitor batches, or the absence of the subtle odors that sometimes hint at insufficient purification. These are the results of intentional process decisions — running extra filtration, tightening the crystallization window, running overnight checks on filtered liquor, and investing in coldroom storage until the final packing.
    Many off-the-shelf materials simply cannot rival this level of consistency. Some manufacturers take shortcuts, stopping purification early or letting higher-than-optimal moisture levels go unaddressed to speed up turnaround. In our experience, customer loyalty comes from performance and clear communication, not flashy marketing or low first-order pricing. Some researchers try cheaper sources for pilot runs, then return after dealing with unpredictability and failures.
    We know every batch of 8-hydroxyquinoline-2-carboxylic acid reflects our own standards. Substituting quality from detailed process control for volume can seem profitable for a time but never lasts. The feedback cycle with users, from university scientists to process engineers to technical buyers, keeps us tuned and honest in our output.

    Looking Forward: Ongoing Improvements and Product Insights

    We view each year as a chance to improve. Routine upgrades to reactor controls, automation in powder transfer, and expanded analytical coverage have been implemented in direct response to both customer commentary and evolving technical standards. We’re exploring options like expanded batch sizes, specialty formulation offers for hard-to-dissolve applications, and new packaging suited for glovebox and automated dosing systems. User feedback shapes what we try next — whether it’s improving drying protocols for ultra-low moisture environments or validating stability in emerging applications.

    This compound brings us regular reminders of why attention to detail and a willingness to listen to end users matters. The lines between production, lab, and application blur as we build the feedback loop stronger. It isn’t the molecule alone, or the synthesis steps, but the way our team meets shifting needs and standards that makes a difference. We will be here, batch by batch, finding new improvements and learning from both success and challenge in manufacturing 8-hydroxyquinoline-2-carboxylic acid.