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3-Hydroxy-2-Naphthoic Acid Hydrazide

    • Product Name 3-Hydroxy-2-Naphthoic Acid Hydrazide
    • Alias Naphthoic Acid Hydrazide
    • Einecs 242-362-3
    • 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

    475563

    Product Name 3-Hydroxy-2-Naphthoic Acid Hydrazide
    Cas Number 1869-10-3
    Molecular Formula C11H10N2O2
    Molecular Weight 202.21 g/mol
    Appearance Off-white to light yellow powder
    Melting Point 299-301°C (decomposes)
    Solubility Slightly soluble in water
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Iupac Name N'-(3-hydroxy-2-naphthoyl)hydrazine
    Synonyms 2-Hydrazinocarbonyl-3-hydroxynaphthalene
    Smiles C1=CC2=C(C(=C1)O)C(=O)C=CC2=NNC
    Inchi InChI=1S/C11H10N2O2/c12-13-11(15)8-5-3-1-2-4-7(8)9(14)6-10(11)13/h1-6,14H,(H2,12,13,15)

    As an accredited 3-Hydroxy-2-Naphthoic Acid Hydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 25g chemical is supplied in a tightly sealed amber glass bottle, labeled with hazard information and product identification for safe laboratory storage.
    Shipping 3-Hydroxy-2-Naphthoic Acid Hydrazide is shipped in sealed, chemical-resistant containers under ambient conditions. The packaging ensures protection from moisture and light. All shipments comply with relevant regulations, including labeling and documentation for safe transport. Handle with personal protective equipment upon receipt. Shipping may be restricted based on destination country due to chemical regulations.
    Storage 3-Hydroxy-2-naphthoic acid hydrazide should be stored in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep it in a cool, dry, and well-ventilated area, preferably at room temperature. Avoid sources of ignition and strong oxidizing agents. Label the container clearly, and handle under appropriate safety protocols, including personal protective equipment.
    Application of 3-Hydroxy-2-Naphthoic Acid Hydrazide

    Applications of 3-Hydroxy-2-Naphthoic Acid Hydrazide in Industrial Manufacturing

    As an established manufacturer, we supply 3-Hydroxy-2-Naphthoic Acid Hydrazide to customers seeking reliable raw materials for advanced chemical synthesis in mature downstream sectors. Our production strictly adheres to international requirements, ensuring consistency and performance in each application. Below, we detail verified industry uses of this intermediate across several targeted manufacturing scenarios.

    1. Organic Pigment Synthesis for High-Performance Colorants

    Specialty pigment producers rely on this compound to synthesize vat and disperse dyes, particularly anthraquinone-based pigments used in automotive, textile, and plastics tinting. The hydrazide group enables direct condensation with aromatic aldehydes under controlled pH, facilitating formation of stable pigment molecules characterized by excellent lightfastness and solvent resistance. Industrial users adjust ratios for desired color intensity and particle size, with consistent batch reproducibility supported by process integration in closed reactors operated under strict safety protocols.

    Industry compliance standards

    • ISO 9001:2015 (Pigment and Dye Quality Management Systems)
    • REACH Regulation (EC) No 1907/2006 for chemical substance registration in Europe
    • ETAD Good Manufacturing Practice Guidelines for Colorants
    • EN 71-3 (Safety of Toys – Migration of Certain Elements, applicable to pigments for toy plastics)

    Typical usage ratio

    • 5–15% by weight in condensation step, adjusted based on molar ratios of co-reactants and pigment strength specifications

    Downstream process integration

    • Charged into pigment synthesis vessel after initial charging of naphthols/aromatic aldehyde and solvent, reacts under alkaline or acidic catalysis, followed by work-up, filtration, drying, and milling to yield finished pigment paste or powder

    Final product types

    • Disperse dyes for polyester fibers
    • Vat dyes for cellulosic textiles
    • Organic pigment dispersions for plastics and coatings
    • Specialty ink colorants for industrial inkjet applications

    2. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Pharmaceutical manufacturers use the hydrazide derivative as a building block in the synthesis of APIs such as naphthyridine antibacterial agents and certain anti-inflammatory drugs. In these processes, it participates in cyclization and condensation reactions that build the molecular backbone of the target compounds. Stringent controls over input purity, reaction time, and lot traceability under GMP conditions are critical for registration dossiers and regulatory approvals in regulated drug markets.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • 21 CFR Part 210 & 211 (US FDA Current GMP)
    • European Pharmacopoeia Monographs for Intermediates
    • WHO Guidelines on Pharmaceutical Production

    Typical usage ratio

    • Varies between 0.7–1.1 molar equivalents in condensation reactions with target aldehydes/acids, with exact amount determined by route-specific stoichiometry and yield optimization

    Downstream process integration

    • Introduced at the cyclization or condensation stage in a multi-step API synthesis, followed by sequential purification and crystallization operations under nitrogen atmosphere to prevent side-product formation

    Final product types

    • Bulk pharmaceutical intermediates
    • Naphthyridine-based APIs (e.g., certain antibiotics and anti-inflammatory agents)
    • Registered finished drug substances after downstream API purification and formulation steps

    3. Corrosion Inhibitor Precursor in Industrial Coatings

    Specialty coatings manufacturers incorporate this hydrazide derivative as a precursor for custom corrosion inhibitors aimed at steel pipelines, equipment housings, and marine paints. Condensation with aldehydes and further chemical modifications result in chelating agents that slow down corrosive oxidation in harsh industrial environments. The intermediate’s quality and consistency directly affect the inhibitor’s solubility, adsorption rate, and long-term barrier protection performance in formulated coatings applied via spraying or dipping.

    Industry compliance standards

    • ISO 12944 (Paints and Varnishes – Corrosion Protection of Steel Structures by Protective Paint Systems)
    • ASTM G31-21 (Standard Guide for Laboratory Immersion Corrosion Testing of Metals)
    • EU CLP Regulation (EC No 1272/2008), Safety Data Sheet compliance for raw material classification and use

    Typical usage ratio

    • Generally 1–3% w/w on total solids content of inhibitor synthesis batch, adjusted for desired inhibitor loading in the end-use paint system and substrate exposure type

    Downstream process integration

    • Added as a starting material in aqueous/organic-phase condensation with aldehydes, then neutralized and filtered before being blended into paint formulations as a corrosion inhibitive additive

    Final product types

    • Chemically modified corrosion inhibitors
    • Anti-corrosive primers and topcoats for marine, automotive, or process industry equipment
    • Protective coatings for industrial piping and storage tanks

    4. Analytical Reagent Synthesis for Laboratory and Environmental Testing

    Chemical reagent manufacturers use this product in the synthesis of analytical reagents designed for selective detection of trace metal ions and organic analytes in water, soil, or industrial effluents. Its hydrazide group enables formation of specific chelates or chromogenic complexes, improving detection limits over classical naphthyl derivatives. Stringent batch-to-batch quality controls guarantee reproducibility of analytical results in standardized laboratory methodologies used by governmental and private labs worldwide.

    Industry compliance standards

    • ISO 17025 (General Requirements for the Competence of Testing and Calibration Laboratories, applicable to analytical reagent suppliers)
    • Reagent grade specifications by American Chemical Society (ACS)
    • OECD Guidelines for Testing of Chemicals (for environmental analysis reagents)

    Typical usage ratio

    • 1–5 mmol/L concentration in reagent formulation, with dosage set according to the analyte type and method detection limit requirements

    Downstream process integration

    • Dissolved into prepared buffer systems, then condensed with target compounds to form chromogenic or chelating reagents which are aliquoted, standardized, and packaged for laboratory use

    Final product types

    • Chromogenic detection kits for metal ion analysis
    • Reagent packs for environmental trace analysis
    • Calibration standards and reference solutions for QC laboratories

    5. Photographic Chemical Formulation for Imaging Material Manufacturing

    Manufacturers of imaging chemicals, especially those specializing in traditional silver halide photography or specialty technical films, use this material in the synthesis of stabilizers and anti-fogging agents. It enters the formulation through coupling reactions that tailor redox potential and improve shelf-life of developing solutions. Strict documentation and traceability requirements extend through R&D and batch QC stages, supporting global distribution in compliance with photographic material standards.

    Industry compliance standards

    • ISO 18902 (Imaging materials – Processed imaging materials – Albums, framing and storage materials)
    • ANSI/NAPM IT9.11 for Photographic Chemicals
    • RoHS (Restriction of Hazardous Substances) for imaging material chemicals in the electronics sector

    Typical usage ratio

    • Ranges between 0.1–0.5% w/v of total developer or anti-fogging formulation, with precise levels optimized according to emulsion type and stability testing outcomes

    Downstream process integration

    • Introduced during stabilizer or developing agent synthesis, subsequently combined with other photoactive ingredients to prepare liquid concentrates or solid developer blends for photographic applications

    Final product types

    • Photographic developers and fixers for black-and-white and color processing
    • Anti-fogging additives for technical imaging films
    • Stabilizing agents for x-ray and industrial imaging materials
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    Certification & Compliance
    More Introduction

    Introducing 3-Hydroxy-2-Naphthoic Acid Hydrazide: Our View from the Factory Floor

    Working with specialty organics for years, a few compounds stand out for their unique performance and reliability. 3-Hydroxy-2-Naphthoic Acid Hydrazide, often marked by the code 3516-18-3, has carved out a trusted space among advanced intermediates. Many of our clients refer to this molecule by its alternative name, β-Hydroxycarboxyhydrazide naphthalene, but on the production floor, the focus stays on consistent yield, color stability, and efficient purification.

    A Close Look at Its Composition and Physical Traits

    This molecule brings together a naphthalenic core with both hydroxy and hydrazide functional groups. The presence of these distinct functional groups creates new windows for downstream chemistry. In our experience, batches yield a pale beige to off-white powder, and quality shifts become obvious during drying or grinding. Consistency here matters—unexpected color change or excess lumping often means impurities, and we apply thin-layer chromatography and melting point checks before considering a lot ready for dispatch.

    We maintain purity levels above 98%, verified by high-performance liquid chromatography and proton NMR. Some customers track water content for their own downstream reactions, and we regularly share our latest Karl Fischer titration numbers. Average particle size remains tight through careful sieving, since caking and attrition alter solubility rates in synthesis.

    Custom Processing for Advanced Application

    3-Hydroxy-2-Naphthoic Acid Hydrazide isn’t a commodity item for bulk blending. Many chemical makers rely on it as a precursor or building block for dyes, pharmaceuticals, and new polymer additives. In our factory, the days typically begin by checking reactor loadings and confirming the hydrazinolysis stage with ongoing infrared spectra. An uncontrolled reaction will shift the hydrazide group formation and lead to isomeric impurities, which complicate analysis for research customers who demand well-characterized side products.

    We dry the reaction mass under vacuum, watching both pressure and temperature to lock in correct water content. It matters more than most new formulators think; too much moisture or residual acid from the prior step will carry over into subsequent acylation or coupling steps. Some buyers request additional micronization; we supply several grain size fractions, as the fineness of the powder alters dispersion in subsequent aqueous or non-aqueous media. Bulk orders ship in sealed fiber drums with extra desiccant, as much for protection against atmospheric uptake as for maintaining batch consistency over longer storage periods.

    Where Real Value Emerges in Research and Industry

    People sometimes ask how this modest-looking compound sets itself apart from similar naphthalenic hydrazides or related hydroxy acid analogs. Our chemists point to the reactivity profile—both the hydrazide and hydroxy moieties open up parallel routes for forming Schiff bases, azo dyes, or as chelators in coordination compounds. The 3-position hydroxy, unlike a 1-hydroxy substituent, improves electron density at both the aromatic ring and the hydrazide, lending extra reactivity during condensation or metal complexation. Downstream applications in dye intermediates benefit from deeper bathochromic shifts compared to isomeric analogs, and the color fastness for textile pigment work eliminates haze and migration that plague inferior precursors.

    Over the years, feedback from certain pharmaceutical groups pointed out how this compound’s well-defined substitution pattern helps them avoid side reactions seen with more generic naphthohydrazides. In anti-inflammatory drug lead generation, a rigid aromatic backbone fits medicinal chemists’ need for aromatic stacking and hydrogen bonding potential. Several research teams highlighted reliable bioassay signals using our material, attributing it to controlled impurity profiles and tight control of alkali residue during final washing.

    Understanding Typical Use Cases and Unexplored Potentials

    For dye and pigment makers, 3-Hydroxy-2-Naphthoic Acid Hydrazide forms the backbone for several high-performance azo and metal-complex dyes. The hydrazide group participates in diazotization, while the hydroxy group offers flexible points for further esterification or etherification. Textile firms tell us the chromophore stability not only gives deeper hues but also stronger washfastness and better light stability. You won’t find as many unexpected color shifts in the finished fabric—a common problem when substituting lower grade precursors.

    Academic customers often explore this intermediate when chasing new chelation complexes or probing structure-activity relationships for enzyme inhibition. Several PhD projects cited our material in their journal papers. We often tweak drying cycles and particle sizing on their request, since their analytical runs depend on batch-to-batch reproducibility. The value comes through when they avoid ambiguous NMR spectra and overlapping HPLC peaks—all thanks to a straightforward synthesis route and close QA oversight.

    Medicinal chemists sometimes test naphthalenic hydrazides as scaffolds in antihypertensive and antimicrobial research. Here, fine control over residual solvents, ash content, and counterion traces means less time troubleshooting unexpected data in downstream assays. Our production team learned to trim the tail-end mother liquor extraction to keep tertiary amines and hydrolyzed side-products to a minimum. Repeated feedback shaped our QA, which now covers not only bulk assay and loss on drying, but also customizable analysis for animal model compatibility and bioactive testing.

    Differentiation from Substitutable Naphthoic Hydrazides

    Customers sometimes wonder why they should pay more for this compound over similar molecules, like 2-hydroxy-3-naphthoic acid hydrazide or unfunctionalized naphthohydrazides. Our folks on the technical team point to its electronic and steric profile: the 3-hydroxy substitution often changes the way it forms linkages—yielding improved coupling efficiency in dye work, higher chelation constants in coordination chemistry, and cleaner, more consistent melting behavior.

    The 2-hydroxy isomers, by contrast, commonly give more tarring during reactions and display greater side-product formation in extended heating. Reports from large-scale pigment synthesis indicate lower batch rejection rates when starting from our product; less off-odor, fewer surface imperfections in pigment dispersions, and more consistent brightness define the end results. In pharma intermediates, a shifted hydroxy group gives access to different conjugates, broadening the scope for library synthesis. Few generic offerings maintain the same level of analytical traceability and batch documentation—something we provide without extra cost, given the value of minimizing surprises during scale-up.

    Hands-on Experience from Years in the Lab and Plant

    The journey from raw naphthalene derivatives to finished 3-Hydroxy-2-Naphthoic Acid Hydrazide involves several careful transformations. The team in synthesis must watch for clean hydrolysis, limiting formation of unwanted tars and over-oxidized byproducts. Years ago, we retooled our filtration section to improve throughput and limit filter cake compaction, after a spate of batches displayed slippage in yield. Operators recalibrated pressure settings and swapped filter media, resulting in less powder loss and drier cakes for quicker isolation.

    Purification and analysis remain a point of pride. Using multiple stages of washing, drying, and bulk sieving, we reduce residual inorganic salts and filterable metals to consistently low levels. TLC runs highlight potential contaminants early in the process. Technicians routinely cross-check final spectra against retained reference samples, helping research customers trace anomalous results to root causes without wasted time.

    Incoming feedback drives improvement. A research partner asked for less residual hydrazine, as GC traces flagged carryover during their bioactivity testing. We modified our washing stage, reducing hydrazine by over 30% without compromising product recovery. Such practical problem-solving, based on real user data, guides our daily decisions on the plant floor.

    Handling, Safety, and Regulatory Observations

    This compound draws added attention for its hydrazide function, given hydrazine’s known safety profile. Production workers, conscious of potential risks, follow closed-system practices, with direct venting on both the hydrazinolysis and drying stages. We invested in vapor monitors and enhanced extraction last year after a simulated spill exercise. Material leaves the plant in UN-rated drums, with certificates of origin and full analysis per lot. These steps keep both our team and the end users protected, but safe storage on-site remains crucial. Spilled powder can cake and release faint odors, so our customers ventilate storage areas and transfer materials using closed canisters.

    Our QA and regulatory staff track changes in local and global registration systems. While this material does not fall under the most restrictive categories, regulatory shifts in hydrazide handling raise periodic questions. Many clients request up-to-date declarations on absence of bisphenol, nitrosamines, or heavy metals, which we supply based on our in-house and third-party analytical runs. Our plant maintains complete batch traceability for several years, easily accessed if REACH, RoHS, or similar documentation ever becomes relevant in the customer’s supply chain.

    Supporting Researchers and Innovators—A Real Partnership

    Research chemists, pigment engineers, and pharmaceutical investigators have distinct needs, and we’ve learned from direct conversation how best to support those needs. Some buyers need technical sheets with detailed impurity breakdowns. Others ask for custom packaging, as their operations run with unique storage limitations. Academic labs often request one-off small packs for early hypothesis testing, preferring smaller batch-to-batch consistency checks over full-blown scale validation. Our production and sales teams avoid automated scripts—a real person calls back to gather context and refine the order.

    This open feedback loop shaped our investment in a new milling unit last year, resulting in tighter particle size boundaries and easier dispersibility for color testing. For pilot-scale pigment projects, we shipped custom 10 kg packs with extra low-moisture barrier film to mitigate clumping during summer transport. In a project with a European university’s medicinal chemistry group, we adjusted our purification protocol to keep total organic residues under their strict safety limits. In each case, direct discussion, quick technical pivoting, and patient quality control closed performance and data gaps before they could grow into bigger problems.

    Watching Out for New Bottlenecks and Charting a Path Forward

    As demand shifts between Asia, Europe, and the Americas, logistics have become more challenging. COVID-era transport backlogs, rapid swings in customs regulations, and climate-driven delays mean lead times occasionally slip outside our usual comfort zone. Our solution draws on diversified raw material contracts, staggered shipping windows, and regular stock level checks—choices shaped by failings of the old just-in-time model. More frequent in-plant inventory reviews and extra buffer stock go further than any dashboard metric in keeping our partners’ projects on track.

    Competition from alternative hydrazides and lower-grade imports puts pressure on price and quality standards. Tricks like masking impurities with optical brighteners or using unfiltered water show up quickly during reaction monitoring. The only constant defense is transparent data on identity, purity, and consistency—records we provide for every drum shipped beyond what regulators demand. Most importers or traders don’t maintain this level of control, and our customers often flag up off-spec issues when experimenting with other suppliers.

    Conclusion: How a Specialty Intermediate Shapes New Capabilities

    The story of 3-Hydroxy-2-Naphthoic Acid Hydrazide isn’t about being generic or commodity-grade. Its value appears in every successful pigment run, every clear research result, and each tight-lot pharmaceutical synthesis. In a sector crowded with copycats and lookalikes, it’s this attention to process, batch quality, safe handling, and technical partnership that makes our product stand out. We remain committed to tracing every raw material source, testing each production run, and tweaking protocols to match shifting industry requirements. The compound’s practical impact—across colorants, pharma, and research—reminds us daily that specialty chemicals demand both technical prowess and a human touch.