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2,4-Dihydroxyquinoline Monosodium Salt

    • Product Name 2,4-Dihydroxyquinoline Monosodium Salt
    • Alias 2,4-DHQ-Na
    • Einecs 629-392-1
    • 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

    525954

    Product Name 2,4-Dihydroxyquinoline Monosodium Salt
    Cas Number 76481-44-8
    Molecular Formula C9H6NNaO2
    Molecular Weight 183.14 g/mol
    Appearance Off-white to beige powder
    Solubility Soluble in water
    Storage Temperature Store at -20°C
    Purity Typically ≥98% (HPLC)
    Synonyms 2,4-Quinolinediol monosodium salt
    Chemical Class Quinoline derivatives
    Smiles C1=CC2=NC(=CC(=C2C=C1)O)O.[Na]
    Inchi Key JQROJYVPVJHPMH-UHFFFAOYSA-M

    As an accredited 2,4-Dihydroxyquinoline Monosodium Salt factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 2,4-Dihydroxyquinoline Monosodium Salt is supplied in a sealed 5-gram amber glass vial, labeled with product details and safety information.
    Shipping 2,4-Dihydroxyquinoline Monosodium Salt is shipped in tightly sealed containers to prevent moisture absorption and contamination. The chemical is packed according to safety regulations, typically with labeling for hazardous materials if required. Packages are cushioned and protected from light, heat, and mechanical shock during transit to ensure product integrity and safety compliance.
    Storage 2,4-Dihydroxyquinoline Monosodium Salt should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, ideally at 2–8°C (refrigerator), away from incompatible materials such as strong oxidizers. Ensure proper labeling, and avoid prolonged exposure to air to prevent degradation. Follow appropriate laboratory safety guidelines during storage and handling.
    Application of 2,4-Dihydroxyquinoline Monosodium Salt

    Applications of 2,4-Dihydroxyquinoline Monosodium Salt in Industrial Manufacturing

    As a direct manufacturer of 2,4-Dihydroxyquinoline Monosodium Salt, we supply this specialty intermediate to advanced industrial customers strictly for applications verified in production pipelines. Below are the most established downstream uses, each reflecting our experience supporting formulation development, scale-up integration, and long-term quality control in regulated manufacturing environments.

    1. Pharmaceutical Intermediate for Quinolone-Based Antibiotic Synthesis

    Our material serves as a building block in multi-step chemical syntheses of certain quinolone antibiotics, where it introduces the crucial heterocyclic dihydroxy functional group through nucleophilic aromatic substitution. Its sodium salt form provides improved solubility and reactivity under controlled reaction conditions typical in active pharmaceutical ingredient (API) plants with validated batch records and validated in-process controls.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP) per ICH Q7
    • U.S. FDA 21 CFR 210/211 (for API synthesis)
    • European Pharmacopoeia (Ph. Eur.) monographs (related intermediates)
    • Quality control under ISO 9001:2015

    Typical usage ratio

    • For API intermediate steps: 1.5–3.2 molar equivalents per target coupling, optimized by target yield and impurity management

    Downstream process integration

    • Added during the early alkylation or acylation steps following initial core construction; dissolved directly in aqueous or mixed solvent media under nitrogen, entering high-shear reactors

    Final product types

    • Quinolone API intermediates (e.g. key intermediates for fluoroquinolone antibiotics such as ciprofloxacin and norfloxacin)
    • Advanced pharmaceutical raw materials

    2. Chemical Standard for Analytical Laboratories

    In accredited analytical testing laboratories, our material functions as a reference calibration standard and an internal standard for purity, dissolution, and trace analysis in the characterization of quinoline derivatives. Laboratories requiring high reproducibility and traceability depend on this intermediate for method development and validation, particularly when analyzing batch release samples for pharmaceutical or specialty chemical customers.

    Industry compliance standards

    • ISO/IEC 17025:2017 (Testing & Calibration Labs)
    • USP General Chapter <621> (Chromatography)
    • Good Laboratory Practice (GLP) as recognized by OECD Principles

    Typical usage ratio

    • Preparation of stock solutions at 0.1–10 mg/mL, adjusted by detection sensitivity in HPLC or UV/Vis assays

    Downstream process integration

    • Dissolution in analytical-grade solvents; used prior to instrument calibration, or spiked in control and validation runs for quantitative assessments in HPLC or capillary electrophoresis workflows

    Final product types

    • Certified analytical reference materials
    • Accredited control samples for pharmaceutical QC labs

    3. Precursor in Agrochemical Synthesis (Plant Growth Regulator Research)

    Specialty agrochemical companies utilize this raw material as a key precursor for synthesis of experimental plant growth regulators based on modified quinoline scaffolds. Its dual hydroxy functionality enables regioselective transformations, critical for downstream derivatization to create novel actives or screen analog series during agroscience research efforts. Tight controls around isolation, handling, and purity monitoring ensure the suitability for pre-commercial pilot scale development.

    Industry compliance standards

    • OECD Good Laboratory Practice (GLP) for Agrochemical R&D
    • EU REACH Regulation (Regulation (EC) No 1907/2006) – substance registration and use reporting
    • ISO 9001:2015 (for process documentation and batch traceability)

    Typical usage ratio

    • Provided at 0.8–2.5 equivalents relative to base aromatic systems, with actual dosage set by screening protocol and yield in target analog construction

    Downstream process integration

    • Fed into condensation or cyclization reactions in reaction vessels under inert atmosphere; used at the core of early step transformations prior to halogenation, amidation, or further functional group modification

    Final product types

    • Quinoline-based plant growth regulator candidates (synthesized for greenhouse screening)
    • Experimental agrochemical leads for structure–activity studies

    4. Colorimetric Reagent Component in Diagnostic Test Kits

    Manufacturers of clinical and food safety diagnostic kits formulate our compound as a primary color-developing agent in proprietary enzyme- or metal-catalyzed colorimetric assay systems for the detection of specific metabolic markers. Chosen for its ability to form stable chromophores under defined assay conditions, the material supports both qualitative and quantitative endpoint readings in single-use and multiwell test formats, requiring tight batch-to-batch control.

    Industry compliance standards

    • ISO 13485:2016 (Medical Device Quality Management for IVD)
    • US FDA 21 CFR 820 (QSR for diagnostic reagents)
    • CLSI (Clinical & Laboratory Standards Institute) guidelines on reagent validation

    Typical usage ratio

    • Formulated at 0.02–0.15% w/w in reagent cocktails, dosage optimized for assay linearity, avoiding interference in target color development range

    Downstream process integration

    • Blended in pre-measured vials or dried in multiwell plate coatings following precision dispensing and lyophilization stages, used in final reaction step before readout

    Final product types

    • Single-use colorimetric diagnostic strips (for clinical or food safety)
    • Multiwell plate assay kits for biomedical research and industrial QC labs

    5. Functional Additive in Antioxidant Formulations for Specialty Polymer Stabilization

    Chemical producers targeting high-value polymer markets make use of the compound as a secondary antioxidant additive during polymer compounding, particularly to enhance UV stability and resistance to oxidative degradation in high-performance engineering plastics. Its phenolic hydroxyls act as hydrogen donors, intercepting free radicals during melt processing or post-curing, and function in synergistic blends with hindered amine light stabilizers for extended service life under demanding conditions.

    Industry compliance standards

    • REACH SVHC non-inclusion status (for use in polymers in the EU)
    • RoHS 2011/65/EU (for electrical & electronics polymers)
    • ISO 11357-6:2018 (Plastics - Differential scanning calorimetry of oxidation)

    Typical usage ratio

    • Loaded at 0.05–0.30% by weight of total polymer mass, varying by polymer matrix type and desired shelf-life extension

    Downstream process integration

    • Pre-dispersed in masterbatch or directly dosed into twin-screw extruders during melt blending, followed by pelletization or direct molding

    Final product types

    • UV-stabilized automotive internal panels
    • Outdoor-rated polymer housings and sheaths
    • Transparent technical films for specialty packaging
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    Certification & Compliance
    More Introduction

    2,4-Dihydroxyquinoline Monosodium Salt: Practical Value through Real Manufacturing Experience

    Our Take: What Sets 2,4-Dihydroxyquinoline Monosodium Salt Apart

    Our production line has a long history with 2,4-dihydroxyquinoline monosodium salt, which we refer to with the internal model code QN-24DHS. Making this compound, we've observed demands from both research and industrial customers who care about batch reliability, solubility, and purity. This is not just another organic intermediate – this is a compound with quirks, utility, and clear-cut differences versus typical quinolines or sodium salts in the specialty chemicals portfolio.

    Our Manufacturing Approach

    Every batch of QN-24DHS starts with rigorous precursor screening. Hydroxyquinolines can carry residues if technicians don’t keep a tight watch on pH during saponification. We use freshly distilled quinoline as the base, avoiding commodity intermediates that often mean trace yellowing or inconsistent sodium content. We don't tolerate haze or particulate; we target a pale, off-white free-flowing powder, usually within 98% purity range by HPLC, and water solubility exceeding 110 g/L at ambient temperatures.

    Our facilities use glass-lined reactors for the hydrolysis and neutralization stages. Stress testing through accelerated heat-aging isn’t a theoretical step for us — we run these tests quarterly. In one run last year, we detected subtle browning after extended exposure to moisture at 40°C, so our R&D group improved drying protocols. Our drums hold less than 0.4% moisture by Karl Fischer titration, which our customers in synthetic biology and high-purity electronics truly notice.

    How Users Deploy QN-24DHS

    QC managers and chemists across fermentation technology, specialty dyes, and advanced material labs reach for this compound due to its versatility. You’ll find QN-24DHS showing up as a chelating agent in all sorts of bioactive molecule syntheses. Some industrial fermenters prefer monosodium versions like ours because multivalent sodiums muddy downstream reactions. It dissolves with minimal stirring, doesn’t foam, and keeps side products at bay, which makes batch-to-batch scale-up much less nerve-racking for operations managers. It’s not uncommon to see survey feedback about its batch consistency, especially from customers who previously bought off-color stuff with erratic sodium content.

    We don’t take for granted the different customer approaches: a university group might buy a single kilogram for a pilot, while process engineers may order fifty times that when scaling a precious metal recovery protocol. We’ve talked shop with clients racing deadlines, troubleshooting their retention times and colorimetric readings. They often call out how predictable this monosodium salt performs, both on its own and parsed into downstream reactions involving aromatic substitutions. That extra degree of confidence, over time, saves workdays and hits client targets.

    Where QN-24DHS Succeeds Over Competing Products

    Contrasting our product with generic dihydroxyquinoline or with buffer-grade sodium salt mixtures, we see three main differences.

    Competitive materials usually trade one benefit for the loss of another. Some suppliers deliver cost-down versions made with lower-grade sodium sources, but their powders build up electrostatic charge in manufacturing and accumulate moisture. That translates into sticky handling in the lab and irregular dissolution profiles. We repeatedly field requests from those burned by such batches, looking to restore a workflow that delivers sharper, more reproducible results.

    Specifications That Impact Workflow

    It’s easy to overlook how a small variation in technical grade can throw off week-long synthesis schedules. For instance, our QA laboratory records all moisture content and sodium assay values per lot, down to ±0.2%. We target a melting point range of 214-218°C, tested by capillary tube, and always confirm absence of non-quinoline-related aromatic impurities on ion-exchange HPLC. We sample all drums for particle size distribution, ensuring no oversized clumps that could mess with automated weighing or mixing equipment.

    Most customers don’t care about a dense product brochure. They want to know: will last week’s run come out like next week’s? For QN-24DHS, we maintain direct records from every batch, sending out a simplified data sheet showing pH (always 7.6 to 8.2 as a 1% aqueous solution), sodium content (single sodium per quinoline by mass spectrometry), and visible color check against a certified pentachlorophenol standard. Rarely do we fail these, but if a shipment throws a curve, we replace or rerun it. This is less about compliance and more about pride in keeping industrial partners moving forward without costly testing repeats.

    Practical Challenges in Manufacturing

    Consistently making QN-24DHS isn’t a matter of setting a fixed process and walking away. Raw material sourcing drives most of the headaches and breakthroughs. Quinoline standards from different suppliers can yield subtle shifts in UV absorbance and impurity profiles. For batches pulled from non-EU, non-US sources, we see up to 0.7% more colored byproducts, making it harder to hit the “off-white” target powder. Not every producer wants to eat the loss or rework a subpar lot, but we scrap those batches, much to our finance team’s regular frustration.

    There are environmental and safety angles, too. Process water used in neutralization needs high purity, low total dissolved solids, and non-detectable chlorine; otherwise, trace halides suppress downstream reactivity. Early in the plant’s life, incoming tap water led to random pink tints in the salt – we now rely only on reverse osmosis–polished supplies and document every water changeover. Customers in microelectronics and biotechnology industries later confirmed that this single switch reduced non-target peaks in assays by measurable degrees.

    Feedback from Those Who Use the Product

    Over two decades, we’ve racked up not only purchase orders but field calls, conference chats, and end-of-quarter troubleshooting sessions. At one symposium, a process engineer described how using a blended sodium salt from a previous vendor led to recurring batch failures in secondary metabolites, only for those failures to vanish after switching to our QN-24DHS. They traced the improvement back to the absence of oxidized aromatic contaminants and the predictability of the sodium-to-quinoline molar ratio. Synthetic chemists highlight our salt’s non-hygroscopic handling in gloveboxes and closed feeders – no more crumbling chunks or live powder spills.

    We invited an academic lab working on oxidative fermentation to tour our plant. They’d reported UV absorption drifts despite using “high purity” product. Walking through our drying, sieving, and sampling process convinced them to specify our model by name, citing “transparency in manufacturing parameters we could actually verify.” That’s real-world vetting — not just spec sheet promises, but consistent, firsthand results.

    Researchers and process managers keep coming back for one major reason: fewer surprises. They want assurance that every box they open — regardless of order size — delivers the same reactivity and solubility.

    Role in Downstream Synthesis and Technology

    In synthetic biology platforms, QN-24DHS often acts as a ligand, shifting reaction equilibria favorably in enzyme-catalyzed steps. Due to its fine-tuned sodium exchange, it doesn’t drag down activity the way dipotassium salts or ammonium analogues do. Typical users spot time savings and yield bumps where this salt takes over a rate-limiting chelation or color stabilization step.

    In dye manufacturing, it holds value as a precursor for crafting photostable pigments—results that depend on zero side-chain impurities. Some pigment trials with less refined hydroxyquinolines showed batch-to-batch color drift and solubility limits. Downstream fabs cut back on QC delays once they shifted to our QN-24DHS because the starting point, time and again, matched their modeled endpoint.

    Rare earth and precious metal extraction outfits discovered that only the monosodium salt maintains high-yield complexation at the pH values required for selective separations. They pointed out that sodium-deficient variants from other plants created a cloud of unpredictable secondary salts, reducing yield and requiring expensive post-treatment. By sticking to our tightly controlled manufacturing, laboratories spend less on excess reagents and filtration steps.

    Tangible Impact through Small Details

    Packing 2,4-dihydroxyquinoline monosodium salt correctly means less mess and fewer headaches for receiving departments. We pack this model in low-static, triple-layered PE bags tucked into sealed HDPE drums. This stems from too many years seeing cracked waxed cartons, powders crusted to the sides, or accidental contaminations from warehouse dust.

    Periodic retesting is not theory for us. We have clients keeping our product in storage for up to nine months, so we retest unopened lots every quarter. Results from last year reconfirmed original purity for 98% of those lots, with the only outliers presenting modest moisture pickup. Users with similar retention requirements see this as a comfort: their reserves hold value rather than degrading and threatening just-in-time production.

    How Differences Matter to End Results

    Maybe it seems like sodium content or color might not matter at the milligram level. But scale up to several tons per year, and micro-impurities cripple project timelines. One glass manufacturer used technical grade from outside suppliers, then shifted to QN-24DHS — batch yields stabilized, and feedback from downstream customer audits improved. Tighter specs on sodium content, along with consistent off-white appearance, reduced time spent on pre-dissolution prep and repeat analysis.

    Many researchers shared that other grades forced workaround steps: double filtration, forced drying, chromatography to remove baseline contaminants. While not every lab faces these pain points, those who do see a clear advantage switching to a monosodium salt crafted for consistency. Material savings, time savings, and a stacked deck toward clean spectra — these benefits ripple outward into cost control and competitive advantage.

    Environmental Stewardship and Worker Safety

    Our site treats effluent from QN-24DHS synthesis via neutralization tanks, with every batch checked for residual organics. Waste stream reduction and sodium recovery aren't afterthoughts — they're part of keeping our plant’s regulatory record clean. Staff in PPE monitor caustic dosing, and every quarterly inspection trains new operators on safe handling, not just of final product but during every point of transfer. Some competitors don't visit the floor daily and miss leak points, but we walk the manufacturing line at every shift start to catch handling issues early.

    Most regulatory touchpoints relate to downstream applications. Biotechnology and dye customers supply increasingly aggressive audit checklists, so we supply Material Trace Certificates for every outgoing shipment. It’s become standard to see R&D leads attending our regular safety reviews — not just our team, but our longest-term customers’ delegates — so data flows both ways, keeping real-world feedback part of the improvement loop.

    Learning from the Front Lines

    Handling and fine-tuning the manufacturing of 2,4-dihydroxyquinoline monosodium salt has made clear over two decades the real, often overlooked, value of craftsmanship in specialty chemicals. What started as a niche organometallic intermediate has proven itself vital in keeping many technologies on time, on spec, and within budget. By responding to feedback, being picky about sourcing, and refusing to send out anything less than tightly spec’d material, we’ve become known as more than just a supplier but a collaborator at the workbench.

    We’ll always see new uses emerging, and as the fields around synthetic biology, pigment innovation, and materials science grow, QN-24DHS continues to show why getting small details right at the manufacturing stage changes what’s possible downstream. Technicians, chemists, and engineers speak frankly with us about their needs because they recognize a kindred approach: sweating details, making peace with setbacks, and always aiming for tangible, reproducible results. That’s what keeps us refining, batch after batch, investing in better outcomes not only for us, but for everyone relying on consistency and purity at scale.