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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 | 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. |
Applications of 3-Hydroxy-2-Naphthoic Acid Hydrazide in Industrial ManufacturingAs 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 ColorantsSpecialty 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
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2. Pharmaceutical Intermediate for Active Ingredient SynthesisPharmaceutical 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
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3. Corrosion Inhibitor Precursor in Industrial CoatingsSpecialty 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
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4. Analytical Reagent Synthesis for Laboratory and Environmental TestingChemical 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
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5. Photographic Chemical Formulation for Imaging Material ManufacturingManufacturers 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
Typical usage ratio
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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.
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.
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.
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.
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.
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.
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.
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.
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.
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.
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.