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3,4-Dihydroxybenzhydrazide

    • Product Name 3,4-Dihydroxybenzhydrazide
    • Alias 3,4-DHBH
    • Einecs 242-572-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
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    Specifications

    HS Code

    384473

    Product Name 3,4-Dihydroxybenzhydrazide
    Molecular Formula C7H8N2O2
    Molecular Weight 152.15 g/mol
    Cas Number 28043-52-7
    Appearance Off-white to light beige solid
    Melting Point 210-214 °C
    Solubility Soluble in water and polar organic solvents
    Boiling Point Decomposes before boiling
    Purity Typically >98%
    Synonyms Protocatechuic acid hydrazide
    Storage Temperature 2-8 °C
    Smiles C1=CC(=C(C=C1C(=O)NN)O)O
    Inchikey PBJXRYKEUDVUKN-UHFFFAOYSA-N
    Pka Around 8.9 (primary hydrazide group)
    Hazard Statements May cause irritation to skin, eyes, and respiratory tract

    As an accredited 3,4-Dihydroxybenzhydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 3,4-Dihydroxybenzhydrazide is supplied in a 25g amber glass bottle with a secure screw cap and tamper-evident seal.
    Shipping 3,4-Dihydroxybenzhydrazide is shipped in tightly sealed containers to prevent moisture and air exposure. It is typically packaged in accordance with safety regulations, labeled clearly, and cushioned to avoid physical damage. The shipment is handled as a chemical reagent, requiring proper documentation and transport according to relevant hazardous material guidelines.
    Storage 3,4-Dihydroxybenzhydrazide should be stored in a tightly sealed container, protected from light and moisture. Keep it in a cool, dry place, preferably at 2–8°C (refrigerator temperature). Ensure storage is away from incompatible substances such as strong oxidizing agents. Proper ventilation is recommended, and access should be restricted to trained personnel to maintain safety and chemical integrity.
    Application of 3,4-Dihydroxybenzhydrazide

    Applications of 3,4-Dihydroxybenzhydrazide in Industrial Manufacturing

    3,4-Dihydroxybenzhydrazide supports production efficiency and output quality across several specialized industrial verticals. The following application scenarios present practical detail on downstream deployment, formulation practices, and regulatory compliance specific to recognized industry standards.

    1. Azo Dye Intermediate for Textile and Leather Colorants

    Textile and leather manufacturers incorporate this compound as a critical hydrazide coupling agent in the synthesis of specialty azo dyes, particularly for high-performance and water-resistant coloring systems. Controlled dosing ensures precision in hue development, while well-established batch or continuous dye manufacturing lines integrate the ingredient at designated reaction stages to achieve consistent chromatic yields for synthetic fibers and processed hides.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • OEKO-TEX Standard 100, Product Class II/IV for textiles
    • EN ISO 17234-1:2015 for leather colorant safety

    Typical usage ratio

    • 0.8%–2.0% by weight of total dye batch; adjusted for target color depth, coupling reactivity, and substrate absorbency

    Downstream process integration

    • Charged into the diazo coupling stage following dissolution and pH adjustment; reacts under controlled agitation and temperature conditions

    Final product types

    • Reactive azo dyes for cellulosic textiles (cotton, viscose)
    • Naphthol-based dyes for synthetic fibers
    • Finished leather colorants for automotive, upholstery, and footwear applications

    2. Organic Synthesis Intermediate in Pharmaceutical API Manufacturing

    This compound is adopted by pharmaceutical ingredient manufacturers as a hydrazide intermediate, particularly in the synthesis of heterocyclic structures with antioxidant or antitumor activity. Its use facilitates scaffold formation for several drug development pipelines targeting chronic and specialty therapeutic classes. Precise metering during the intermediate step ensures the stability and bioavailability of the finished molecule.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) general monographs
    • US FDA cGMP 21 CFR Part 211, Part 210
    • Chinese Pharmacopoeia (ChP) requirements on chemical intermediates

    Typical usage ratio

    • 0.5–1.5 molar equivalents relative to the ketone or aldehyde reactant; dosage depends on target yield and impurity profile control

    Downstream process integration

    • Introduced during early condensation or cyclization stages in multi-step organic synthesis, typically under inert atmosphere; purified before use in downstream final API manufacturing

    Final product types

    • Precursor for hydrazone-based APIs (e.g., cytotoxic agents, enzyme inhibitors)
    • Substituted benzotriazoles and heterocyclic pharmaceutical scaffolds
    • API intermediates for custom synthesis contracts

    3. Corrosion Inhibitor Additive in Industrial Water Treatment

    3,4-Dihydroxybenzhydrazide enters industrial closed-loop water systems as a corrosion inhibitor, where its chelation properties contribute to the protection of metal surfaces in heat exchangers, cooling towers, and boiler feed circuits. Water treatment operators monitor dosing in accordance with real-time system diagnostics to suppress scale and oxidation while maintaining compliance with effluent quality mandates.

    Industry compliance standards

    • ASTM D1384 Standard Test Method for Corrosion Testing of Engine Coolants
    • ISO 5667-10:1992 for water sampling in industrial use
    • EU Industrial Emissions Directive 2010/75/EU (IED) for wastewater management
    • US EPA 40 CFR Part 423 Steam Electric Power Generating Effluent Guidelines

    Typical usage ratio

    • 10–45 ppm (mg/L) in circulating water streams; adjusted based on system metallurgy, water chemistry, and flow rate

    Downstream process integration

    • Metered via dosing pumps directly into recirculating water lines or batch-mixed during system start-up; validated by online corrosion rate and residual inhibitor concentration measurements

    Final product types

    • Industrial circulation water blends for power generation
    • Boiler feedwater additive packages
    • Cooling tower inhibitor formulations for petrochemical and manufacturing plants

    4. Analytical Reagent for Metal Ion Detection

    In laboratory and quality control environments, chemists employ 3,4-Dihydroxybenzhydrazide as a selective reagent for photometric or colorimetric detection of trace metal ions, especially iron(III). The compound reacts under controlled buffer conditions to produce distinct chromophores, facilitating accurate quantification in water analysis and resource extraction process monitoring.

    Industry compliance standards

    • ISO 6332:1988 for determination of iron by spectrometric methods
    • EPA Method 200.9 for trace elements analysis in water and waste
    • ASTM D1068 for iron in water by 1,10-phenanthroline and similar reagents
    • GLP and ISO/IEC 17025 laboratory accreditation procedures

    Typical usage ratio

    • 10–40 µmol per 50 mL analytical sample; reagent dosage modulated based on detection limit and matrix complexity

    Downstream process integration

    • Dissolved into buffered sample aliquots and combined with target solution during spectrophotometric measurement; handled by trained laboratory staff under validated SOPs

    Final product types

    • Colorimetric test kits for environmental field water testing
    • Analytical reagents for certified reference laboratories
    • Process monitoring kits for mining and metallurgical operations

    5. Polymeric Material Cross-Linker in Specialty Resin Formulation

    Manufacturers in the advanced materials sector utilize 3,4-Dihydroxybenzhydrazide as a multifunctional cross-linker for heat-resistant polymer resins. Its dihydroxy and hydrazide moieties enable durable covalent bonding in thermoset systems, improving mechanical stability and thermal cycling resistance for coatings and high-performance composites manufactured under tightly controlled conditions.

    Industry compliance standards

    • ISO 9001:2015 for quality management in polymer manufacturing
    • REACH Annex XVII restrictions for use in polymers
    • UL 94 flammability standards for finished polymer goods
    • EN 13501-1:2018 for fire classification of building materials

    Typical usage ratio

    • 0.5%–1.2% by weight of total resin solid content, optimized based on cross-link density, flow characteristics, and curing cycle

    Downstream process integration

    • Dosed during compounding stage; blended with base resin and curing agents before thermal or UV curing following established process parameters

    Final product types

    • Thermosetting coatings for industrial machinery
    • Composite matrix resins for automotive and aerospace parts
    • Protective films for electronics and appliance housings
    Free Quote

    Competitive 3,4-Dihydroxybenzhydrazide prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    3,4-Dihydroxybenzhydrazide – A Closer Look from the Manufacturer’s Bench

    Our Approach to Making 3,4-Dihydroxybenzhydrazide

    Every batch of 3,4-Dihydroxybenzhydrazide coming out of our facility carries the signature of our team’s experience in fine organic synthesis. Over years in the chemical industry, we have developed a synthesis route for this compound that offers consistent purity and minimizing batch-to-batch variations. The model we currently supply meets demanding requirements encountered in pharmaceutical research and advanced material development. It makes sense for those in need of reliable, high-quality intermediates to understand what sets this compound apart from standard hydrazide derivatives.

    3,4-Dihydroxybenzhydrazide starts with a specially selected precursor: 3,4-Dihydroxybenzoic acid. Our technicians use hydrazinolysis under controlled temperature and pH, watching for by-product formation and monitoring the reaction to meet strict purity standards. The resulting compound emerges as a crystalline solid, off-white to pale tan, easily distinguished from other similar products by the ease of filtration and washing at our scale.

    Manufacturing fine chemicals isn’t just about following procedures. It takes experience to know how much washing is enough or what a “clean” endpoint should look like for this hydrazide. We use in-process HPLC and TLC checks to confirm the proper completion of the reaction. Our team uses FTIR and NMR for every final batch — not every plant can make guarantees based on first-hand analysis, but we run our own equipment and rarely outsource quality controls.

    How This Compound is Used

    3,4-Dihydroxybenzhydrazide gets the attention of pharmaceutical chemists and materials researchers because its catechol and hydrazide functional groups allow for further derivatization. In drug design, the molecule provides an easy platform for building new hydrazide-containing derivatives. Researchers have reported its use in synthesizing metal chelates, enzymatic probes, and as a precursor for antioxidants. The ortho-dihydroxy substitution pattern opens up additional hydrogen-bonding possibilities, important for making enzyme inhibitors or advanced ligand scaffolds.

    We often talk directly with formulating chemists looking for reliable hydrazides. Reports from our customers show the compound serves well as a starting point for synthesizing complex hydrazones, azines, and heterocycles. Conventional benzhydrazide doesn’t carry the same reactivity as our 3,4-dihydroxy model, lacking the ability for further modifications on the aromatic ring — a feature our clients find vital for late-stage functionalizations.

    Analytical teams looking to develop diagnostics or colorimetric assays also choose our 3,4-Dihydroxybenzhydrazide for its electron-rich structure, which interacts strongly with metals and biological substrates. This opens up routes for a new generation of chemosensors, especially in contexts where sensitivity to iron, copper, or other transition metals matters. A standard hydrazide can’t offer these conjugation opportunities since those lack the necessary ortho-phenolic hydroxyls.

    Specification and Purity Control: From Raw Material to Final Product

    With our facilities, the typical batch is manufactured to meet a minimum purity of 99 percent by HPLC. Color, melting range, and solubility tests run on every lot keep us confident those purchasing the compound get an identical product each time. We do not tolerate contamination with oxidized catechols or partially reacted intermediates. Infrared spectra of our batches show clear, sharp N-H and O-H stretches, confirming the presence of all functional groups and excluding unreacted or degraded starting materials.

    Particle size distribution tends to be narrow; the finished product runs through a controlled-size reduction, making handling simple for both lab and pilot plant scales. We go beyond standard sieve analysis. Our operators watch for clumping or abnormal dust generation, making sure that physical form supports accurate dosing and mixing, since formulation scientists sometimes need to get precise reproducibility at the scale of milligrams.

    Moisture content receives special attention. Many buyers of generic hydrazides complain about caking or inconsistent weights—problems rarely encountered with our product, because controlled drying and sealed packing leave little room for error. On the rare occasions we get queries about shelf stability, we can pull results from ongoing stability tests, showing that properly stored compound resists moisture pickup and decomposition for typical storage periods. We use tight, light-filtering containers to minimize any photodegradation, a detail that matters when working with phenolic substances.

    Direct Differences: 3,4-Dihydroxybenzhydrazide versus More Common Hydrazides

    After years making both unsubstituted benzhydrazide and a range of dihydroxy-derivatives, distinctions become clear. Unsubstituted benzhydrazide, often chosen for volume-driven applications, can’t offer the ortho-hydroxy reactivity profile. The 3,4-Dihydroxy form rapidly forms complexes with transition metals and participates in condensation reactions under milder conditions. This enables greater selectivity and shorter synthesis times for downstream chemistries, especially in medicinal chemistry and sensor design projects.

    Our model succeeds in downstream reactions other hydrazides struggle with. The electron-donating hydroxy groups help activate the benzene ring, easing reactions with electrophiles and facilitating oxidation or cross-coupling. In contrast, standard benzhydrazide often yields lower product in challenging N-acylation or arylation steps; the ortho-dihydroxy can act as a built-in “enhancer” for these transformations.

    Not all customers have tackled the issue of by-product separation the way we have. After synthesizing both standard and dihydroxy hydrazides, our team recognized that excess hydrazine or partial hydrolysis products stick around more often in basic benzhydrazide runs. Our current protocol for the 3,4-dihydroxy version ensures these side products are washed out. That makes downstream reactions run with fewer surprises.

    Applications and Experiences from the Lab Floor

    Our customers span several industries. We see orders from teams working on first-in-class enzyme inhibitors, as well as groups focused on functional polymer synthesis. By keeping lines of communication direct with lab chemists and project managers, we hear which features of this compound matter most.

    A synthetic chemist in a pharmaceutical lab shared that the ready solubility of 3,4-Dihydroxybenzhydrazide in both water and polar solvents allowed faster parallel reactions. Processing time—and reactant waste—drops noticeably compared to runs with more hydrophobic hydrazides. A team working on metal ion sensors confirmed that the ortho-hydroxy groups facilitate robust chromogenic shifts; these changes become easy to monitor and automate. Several polymer chemistry teams commented on the way coupling reactions proceed without the stalling seen with mono-substituted hydrazides.

    Some of our oldest clients value consistency. In multi-step syntheses, where each stage might take weeks, an inconsistent batch can waste both time and money. By keeping analytical oversight in-house, our team cuts the risk of out-of-spec batches reaching the customer. On occasions where customers have had trouble with third-party supplied dihydroxyhydrazides—usually citing mixed melting points or unpredictable odors—we’ve provided side-by-side samples as proof. Repeat customers tend to stick with us for this kind of reliability.

    Sustainable and Safe Scalability in Manufacturing

    Not every synthesis easily transfers from the lab to production scale. Over the years, we have faced common challenges, from foaming during work-up to oxides forming at unexpected stages. Each manufacturing run contributes learning—these lessons show up in our protocols as modifications to agitation speed and solvent ratios.

    Our scale-up process for 3,4-Dihydroxybenzhydrazide responds to both environmental and workplace safety expectations. We minimize use of corrosive agents, recycle process solvents, and dispose of aqueous waste streams in line with strict local environmental codes. Safety data gets reviewed with every shift, and the team receives regular refreshers on hydrazine handling and spill control.

    For clients planning larger campaigns, shipping large quantities calls for close cooperation between our production specialists and supply chain partners. We only use certified drums, and every container is pressure-tested. Shipping documentation goes out with each order — on several occasions, our customers' compliance teams have noted the completeness of our delivery history and analysis files.

    Addressing Common Challenges with 3,4-Dihydroxybenzhydrazide

    Quality isn’t just about assay numbers. Past production runs exposed subtle pitfalls: slow crystallization rates, changes in color suggesting oxidative instability, and formation of tars in storage. To solve these, our R&D staff pushed for lower reaction temperatures and introduced controlled atmospheres at sensitive stages. December batches sometimes required extra cooling to eliminate color drift—a practice now part of every protocol. Unreacted starting materials tend to produce off-odors; our extended vacuum drying at the finish removes these traces and results in a product that is as chemically clean as it looks.

    Some buyers raised concerns about potential trace metals or leftover solvent. We responded by setting internal specs well below regulatory limits, running every lot through ICP-MS and GC headspace analysis. Over the years, questions about elemental contamination dropped off, as test results showed compliance with even the strictest customer standards.

    All production steps happen in our own facility. We invite customer audits, and new partners often notice the level of automation in our operation: tracked batch entries, RFID-tagged raw materials, and real-time digital monitoring of reaction conditions. We believe in giving customers clarity about what they receive, and that means answering technical and regulatory questions promptly, supported by real batch data.

    Looking Forward: Improving the Process and Pushing Applications

    No process stays perfect forever. We keep testing greener alternatives for solvents and workup agents. Our R&D group experiments with flow chemistry for small-scale lots, reducing reaction time, waste, and improving work-up safety. Equipment upgrades often get driven by small but frequent challenges raised by customers—caking in the shipping drum, static electricity buildup on cold days, or difficulty opening sealed bags in humid environments.

    Many researchers using our 3,4-Dihydroxybenzhydrazide have requested larger sample sizes for preclinical studes or pilot production. To meet this, we invested in modular reactor systems that enable fast turnaround without compromising the hands-on oversight unique to our team’s craft. Transparency with customers about shipping times and capacity remains one of our strengths.

    Calls for longer shelf life and easier handling pushed us to modify our packaging. We switched from plain foils to multilayer pouches with built-in desiccants. Clients benefit from less clumping and extended product life, particularly in humid regions.

    The Value of Direct Manufacturer Experience

    Having control of every batch gives us insights no distributor can offer. We recognize which process tweaks affect not just yield, but useability for chemists who push the boundary of drug discovery or materials science. Many of our improvements trace back to end-user discussions—requests for more rigorous documentation, finely milled powder, or additional test data.

    Troubles with off-branded hydrazide analogues—unstable solids, irregular particle size, or suspiciously high impurity readings—have brought some clients to our door seeking a long-term solution. With direct manufacturing expertise, we can do more than supply a reagent: we build partnerships based on clear technical dialogue. Our team isn’t shy about sharing real production challenges and their solutions, because ongoing quality is built on transparency and adaptation.

    From start to finish, manufacturing 3,4-Dihydroxybenzhydrazide in our facility means taking responsibility for each stage, from raw material sourcing through final test reporting. Each customer batch reflects a commitment to precision and openness—not just a desire to ship material but to support its success in every downstream application. This hands-on philosophy drives us to keep improving synthesis, handling, packaging, and support—challenging ourselves to deliver an ever better product year on year.