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HS Code |
652841 |
| Chemical Name | 2,4-Dihydroxybenzhydrazide |
| Cas Number | 59546-46-4 |
| Molecular Formula | C7H8N2O2 |
| Molecular Weight | 152.15 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 214-216 °C |
| Solubility | Soluble in water, ethanol, and DMSO |
| Structure | Benzene ring substituted at 2 and 4 positions with hydroxyl groups and a hydrazide (-CONHNH2) group |
| Synonyms | 2,4-Dihydroxybenzohydrazide |
| Storage Conditions | Store at room temperature, in a tightly closed container, protected from light |
As an accredited 2,4-Dihydroxybenzhydrazide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2,4-Dihydroxybenzhydrazide is packaged in a sealed 25-gram amber glass bottle with a tamper-evident screw cap. |
| Shipping | 2,4-Dihydroxybenzhydrazide is shipped in tightly sealed containers, protected from moisture and light. It is typically packed according to standard chemical safety regulations, with proper labeling and documentation. Shipping should comply with international and local regulations for laboratory chemicals, ensuring the material remains secure and undamaged during transit. |
| Storage | 2,4-Dihydroxybenzhydrazide should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers. Protect the chemical from light and moisture. Proper labeling and handling with appropriate personal protective equipment (PPE) is recommended to prevent exposure and contamination. |
Applications of 2,4-Dihydroxybenzhydrazide in Industrial Manufacturing2,4-Dihydroxybenzhydrazide serves precision roles in several specialized industrial sectors. As the actual producer, we supply to manufacturers that integrate this compound for its specific functional performance across chemical syntheses, dye manufacturing, pharmaceutical intermediates, advanced analytical reagents, and polymer chemistry. The following sections detail how our partners incorporate this raw material into diverse production environments. 1. Pharmaceutical Intermediate SynthesisIn pharmaceutical manufacturing, 2,4-Dihydroxybenzhydrazide functions as an advanced building block for certain APIs and specialized heterocyclic intermediates. Leading API producers employ our material in the hydrazinolysis step, forming key linkages in anti-inflammatory and antibacterial compounds. The compound’s purity and residue profiles align with stringent pharma requirements, and it passes full traceability audits. Process engineers introduce the substance during the core coupling reaction, with real-time in-process control ensuring batch reproducibility and clean downstream isolation. Our material contributes to the core structure of cephalosporin and quinazoline derivatives, supporting manufacturers seeking competitive lead times and regulatory acceptance. Industry compliance standards
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2. Azo and Heterocyclic Dye SynthesisColorant producers utilize our hydrazide derivative as a coupling component for laboratory and industrial azo dye production. Chemical engineers react it with aromatic diazonium salts to generate a spectrum of specialty colorants with high solubility and thermal stability. The substance enters the workflow in the main coupling step, where control of temperature, pH, and stoichiometry directly affects the resulting dye purity and shade index. Its performance allows for the consistent tone required in fiber-reactive and indicator dyes used by textile, printing, and analytical reagent manufacturers. Industry compliance standards
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3. Polymer Modification and Chain ExtensionPolymer manufacturers incorporate this hydrazide in specialty copolymer and chain-extension reactions, particularly for enhancing aramid and polyamide materials. It acts as a reactive linker and chain stopper, modifying polymer backbone rigidity or enabling the design of target functional groups for membrane and filtration applications. Production staff dose the product at the oligomer fusion stage under controlled thermal profiles, ensuring full reactivity without compromising polymer molecular weight distribution. The careful balance of feed rate and hydrazide content determines crosslink density and final elongation properties in the processed polymer. Industry compliance standards
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4. Analytical Reagents and Chemical DerivatizationManufacturers specializing in laboratory reagents deploy 2,4-Dihydroxybenzhydrazide as a core component in reagent kits for spectrophotometric, chromatographic, and detection assays. The compound serves to derivatize aldehydes and related carbonyl groups, facilitating precise quantification and improving analyte stability during sample preparation. Production chemists measure and add the powder into buffered reagent concentrates, where its reactivity and minimal impurities guarantee reproducibility required by certified testing labs and regulatory bodies. The product impacts downstream kit lot approval rates and reliable QC performance for both industrial and clinical settings. Industry compliance standards
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Our work with 2,4-Dihydroxybenzhydrazide has grown from years spent balancing market expectations with raw chemistry. This compound, known in technical settings for its solid hydrazide backbone and specific hydroxy substitutions on the benzene ring, comes with more than textbook promise. After handling the product in batch and continuous settings, we see its advantages and quirks play out in day-to-day production and use.
2,4-Dihydroxybenzhydrazide, sometimes referenced by chemists using its CAS number or synonyms in the literature, starts its journey on the bench—often from dihydroxybenzoic acid or related derivatives. The chemical formula, C7H8N2O3, might seem simple, but those two hydroxy groups at positions 2 and 4 make a significant difference in reactivity compared with mono-substituted analogues. Our usual production method employs a hydrazinolysis approach using carefully-controlled temperature and stoichiometric ratios, which produces a consistent white crystalline powder. Every kilogram produced owes its quality not to automation, but to the eyes and hands that monitor purity, moisture, and granule size.
We measure melting range, purity by HPLC, and water content batch by batch, never just taking a previous COA as gospel. The product exhibits a melting point typically around 230°C, with our best lots holding purity over 98% by area. Observing the color, particle flow, and even “feel” of the powder is still part of our QA. This hands-on approach finds contaminants or irregular batches that analytical machines sometimes miss.
Most standards for 2,4-Dihydroxybenzhydrazide center around its use in synthesis labs, pilot plants, or as a research intermediate. Moisture control, dusting potential, and shelf stability matter for operators who spend shifts weighing and mixing—especially if material sits in hoppers or open trays. We have adjusted our drying cycles and packaging to keep caking to a minimum, based on feedback from our own team and end users alike.
Chemists buy 2,4-Dihydroxybenzhydrazide mostly for its role as an intermediate in pharmaceuticals, specialty colorants, and metal chelation studies. Each field pushes for narrow specifications. Pharmaceutical projects use it during heterocycle construction or as part of condensation reactions to introduce controlled hydrazone or oxadiazole functionalities. We supply regular consignments to R&D centers working on anti-tubercular and antifungal agents. The hydroxy groups offer anchor points for selective modification, and the hydrazide moiety opens the door to N-N linked molecule families.
In pigment and dye development, our product has been called on for benzoxazinone formation and azo dye research. The position of its hydroxyl groups enables electronic effects different from 3,4- or 2,5-analogues, with colorists seeking shifts in absorption spectrum or material fastness. Our customers have reported that switching from plain benzhydrazide to our 2,4-dihydroxy variant affects shade purity and stability under accelerated aging. For these users, any trace of alkali, heavy metals, or residual solvents causes waste or outright batch failure, which is why we never cut corners on washing and drying.
Working with academic and industrial customers, we have seen 2,4-Dihydroxybenzhydrazide tested in analytical sample preparation, often for metal ion complexation. Its chelating ability, stemming from the spacing of hydrazide and phenolic groups, attracts attention in trace analysis of environmental pollutants—especially heavy metals like copper or nickel. Small changes in crystalline structure or surface area alter chelation efficiency, so we routinely run test reactions in-house beyond required specifications to flag such variation before shipment.
Chemists sometimes ask why not substitute other positions or hydrazide derivatives. The practical answer lies in the compound’s reactivity profile and solid-state behavior. The 2,4-dihydroxy variant differs in hydrogen bonding and resonance stabilization from, say, the 2,5- or 3,4- isomers. The 2,4-setup produces stronger chelating effects and different electron-donating properties, shifting how it reacts in condensation or cyclization steps. We see tangible differences in yield and side product formation between similar molecules, and so do our clients.
Another factor: solubility in key solvents. Our product dissolves consistently in hot methanol and ethanol but resists dissolving in cold water—a trait that can be used to control recrystallization or separation steps. In formulations where solvent choices are dictated by downstream process safety, knowing actual solubility parameters and batch-to-batch behavior gives formulators an honest edge. Working directly with our material rather than through trading companies, customers provide feedback that helps us tweak our protocols, closing quality loops in physical and chemical performance.
Other hydrazides fall short in some applications because they lack reactive sites or their by-products introduce undesirable residues, especially for pharmaceutical intermediate routes. By manufacturing at source and tracking not just the final product but impurity profiles and process residues, we help chemists plan scale-ups based on what really happens, not just published specs.
In our plant, producing 2,4-Dihydroxybenzhydrazide means balancing yield with purity. The hydrazinolysis route can push up unwanted side products if temperature or input quality slip. We have mapped reaction progress using at-line analytics, and occasionally see batch-by-batch variation in trace impurities—some hydrazides are especially sensitive to iron or copper ions introduced from stainless or non-lined vessels. Switching to glass lining in critical steps dropped a persistent impurity peak by more than 80% in our experience, which improved downstream reactivity for one client’s synthesis stage.
Another issue often overlooked involves packaging. Our packaging team regularly inspects for micro-holes in polyethylene liners or jar seals. Humidity, once it finds a way in, causes caking or even hydrolysis. Feedback from a customer using the compound in high-precision synthesis led us to modify the drying protocol, extending vacuum drying by several hours during summer months. Consistency in powder flow and stability improved sharply as a result, which makes handling easier and keeps the upstream processes running smoothly.
Waste management requires thought, as hydrazine and derivatives demand careful handling for safety and environmental reasons. Our site enforces full capture and neutralization protocols for hydrazine vapor, with self-audits occurring twice per month. Sludge or washings are processed in an on-site treatment facility, and we report solvent recovery rates as part of our annual performance audit. By doing so, we protect both our workers and the communities around us—as well as buyers who care about sustainable sourcing or regulatory compliance.
We tailor process parameters based on past real-world outcomes, not theoretical models. Years back, operators noticed certain batches of 2,4-Dihydroxybenzhydrazide showed odd discoloration after prolonged storage. Analytical follow-up found minor oxidation at the ortho-hydroxy position, so we shifted to nitrogen-blanketed storage for both finished product and intermediates. After this change, returns dropped and shelf life estimates became more accurate. This example highlights a basic truth: making a specialty intermediate is not only about running a reaction but knowing what can go wrong, catching it, and fixing it.
As hands-on chemical manufacturers, we do not simply analyze a sample or review test data. Every lot receives close inspection by our veteran operators, who understand the difference between a batch that “looks right” and one that might seem fine on paper but behaves poorly in actual use. Customers have told us that our product handles more cleanly in automated dosing and minimizes downtime in continuous feeders compared with purchases from re-baggers or traders.
Our specification sheet is written in plain language and backed by years of actual production. Particle size is set based on what customers report works best for their mixing and transfer systems—not arbitrary standards. Solvent residues fall well below international limits, and every consignment is accompanied by a full chromatogram, not just a simple number, so buyers see the same data we do. This transparent approach builds trust and keeps technical and purchasing teams on the same page.
Within our experience, direct competitors often substitute with lower-purity benzhydrazides or multi-hydroxy analogues when sourcing from non-manufacturing intermediaries. This shortcut may save costs but introduces risk. We have seen batches from traders containing inconsistent isomer ratios or metal ion contamination, both of which undermine yields in delicate synthesis steps. With regular process adjustments, our plant controls for these risks at the source, reinforcing the value of a manufacturer-managed supply.
Other products in the same category, such as 3,4-dihydroxybenzhydrazide or unsubstituted benzhydrazide, show different reactivity patterns and stability profiles. For instance, the 3,4-isomer’s electron distribution alters its condensation speed and selectivity, often shifting product purity by several percent unless handled with matched process conditions. Our clients—especially those in medicinal chemistry—prefer 2,4-dihydroxy due to its predictable handling, cleaner reactions, and well-characterized impurity footprint.
We respond to requests for customization—not just by adjusting purity or particle size, but by tuning solvent residues, granulation, and even color as requested. There have been several collaborations with university groups where selective modification led to unique active ingredients or functional materials unobtainable by standard catalogue items. In these assignments, turnaround speed matters. Because we own and operate the facility, we can scale from gram to ton as needed, integrating feedback from lab-scale trials into commercial-scale batches. This flexibility serves research-driven markets and applied industries alike.
Practical feedback from pharmaceutical validation teams and industrial processors helps us spot where a lot performs above or below expectations. We keep records of every complaint, return, or report of handling issues, using these to drive upgrades in process and QA. Recent shifts in regulatory limits for hydrazide impurities in certain jurisdictions pushed us to further reduce carry-over from starting materials, which required refining extractive washes and upgrading vacuum filtration. These changes, though costly, reduced complaint rates and opened up new markets needing even tighter specification control.
Not every improvement comes from customer audits; many arise internally. One operator flagged a recurring, subtle odor to a batch that passed all regular tests. Our QA team tied this back to trace solvents from a supplier’s change in raw material preparation, prompting us to add an extra purification step. This experience reinforced the value of hands-on awareness at every stage and the limitation of relying solely on test results.
From collaborations with academic and industrial researchers, we gained insight into structure-activity relationships—how spatial arrangement of hydroxy and hydrazide groups affects chelation, condensations, and stability. The 2,4 substitution consistently outperforms in chelation studies targeting water purification applications, attributing to its favorable ligand geometry. This feedback loop with actual users pushes us to refine protocols and further define grade options suited to ever-diversifying applications.
Having direct control of production and quality gives our clients peace of mind, whether they are running pilot reactions, scaling to clinical manufacture, or synthesizing specialty pigments. Changes in global supply routes often introduce uncertainty when product is sourced through traders or brokers. Our ability to keep process transparency, trace residues, ensure batch consistency, and deliver thorough technical support comes from owning the entire manufacturing chain. This foundation breeds reliability—and ultimately supports faster approvals, fewer recalls, and lower risk in regulated and non-regulated applications alike.
We view every order as more than a simple shipment—each unit shipped stands as a result of coordinated effort from chemists, operators, QA staff, and logistics experts. Knowing which subtle factors matter—particle flow, absorption rate, trace impurity impact—ensures buyers end up with material that performs consistently. Experienced formulators often report a smoother transition on scale-up and fewer unexpected technical setbacks than with goods sourced from re-packers or importers.
Beyond technical specs, we give open access to lot histories and real-time QA statistics. Our documentation includes the actual test data, chromatography, and a breakdown of deviations when they occur. Clients have the benefit of reviewing primary data, seeing exactly how the material will behave in their own facility based on real production records, not just generic promises.
Supporting each batch, we provide on-request application notes, highlighting relevant literature findings and firsthand experiences from field work. Questions on reaction mechanisms, impurity management, or application-specific troubleshooting receive detailed responses, directly from our in-house chemists, not from detached customer service reps. This tight feedback loop enables buyers to plug material into their process lines with minimal risk and quick adaptation.
Ongoing investments in in-process controls, better analytical tools, and operator training keep 2,4-Dihydroxybenzhydrazide at the required standard for the world’s researchers and manufacturers. As market needs evolve—including the drive for greener processes, lower impurity footprints, and new functionality—our manufacturing process adapts. Regular engagement with buyers and research partners ensures our products grow alongside application demands.
We welcome direct inquiries about application experience or potential modification. By maintaining open lines between shop floor, laboratory, and end user, we build knowledge and partnerships that last through both routine orders and one-off challenges. With an open-door approach and a solid manufacturing backbone, we push forward the science and business of 2,4-Dihydroxybenzhydrazide for those who rely on honest, accountable supply—and real-world performance.