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HS Code |
764394 |
| Cas Number | 610-39-9 |
| Molecular Formula | C7H4N2O6 |
| Molecular Weight | 212.12 g/mol |
| Iupac Name | 3,4-dinitrobenzoic acid |
| Appearance | Yellow crystalline powder |
| Melting Point | 205–208 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.69 g/cm³ |
| Pka | 2.57 |
| Pubchem Cid | 74008 |
| Synonyms | m,p-Dinitrobenzoic acid |
| Hazard Statements | Irritant, harmful if swallowed |
| Storage Temperature | Store at room temperature |
As an accredited 3,4-Dinitrobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 3,4-Dinitrobenzoic Acid; airtight cap, hazard labels, and specification details on label. |
| Shipping | 3,4-Dinitrobenzoic Acid is shipped in tightly sealed containers, protected from moisture and light. Packages are clearly labeled with hazard information due to its classification as an irritant and potential environmental hazard. Shipping complies with local and international regulations, often requiring handling by trained personnel and appropriate documentation for safe transport. |
| Storage | 3,4-Dinitrobenzoic acid should be stored in a tightly sealed container, in a cool, dry, well-ventilated area, away from sources of ignition and incompatible substances such as strong bases or reducing agents. Protect from light, moisture, and physical damage. Label containers clearly and follow all safety guidelines, using secondary containment if necessary to prevent spills or leaks. |
Applications of 3,4-Dinitrobenzoic Acid in Industrial ManufacturingAs a specialized manufacturer, we supply 3,4-Dinitrobenzoic acid for advanced chemical synthesis across multiple sectors. The following application scenarios have been established through collaboration with end users, guided by rigorous quality control and compliance processes. 1. Synthesis of Veterinary Pharmaceutical IntermediatesMajor pharmaceutical companies employ 3,4-Dinitrobenzoic acid in the synthesis of active and intermediate molecules for veterinary antimicrobials and antiparasitics. This compound functions as a nitroaromatic precursor during nitration and reduction steps, forming the backbone of complex drug molecules. Compliance extends to international pharmacopoeias, while process engineers continually optimize the usage ratio based on target yield and impurity profiles. Industry compliance standards
Typical usage ratio
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2. Manufacturing of High-Performance Polymer AdditivesThe specialty plastics and elastomers sector uses this raw material within custom additive packages, especially where nitro functional groups enhance degradation resistance or facilitate molecular crosslinking. It enters the compounding stage for engineering polymers, with usage tightly controlled for batch homogeneity and migration limits, adhering to chemicals safety guidelines for polymer processing. Industry compliance standards
Typical usage ratio
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3. Analytical Reference Material ProductionCertified reference material (CRM) producers incorporate 3,4-Dinitrobenzoic acid as a high-purity standard for quantitative laboratory applications. Laboratories utilize it to calibrate detection methods for complex organic mixtures, especially in pharmaceutical residue and environmental contaminant screening. The production follows strict ISO accreditation for traceability and analytical confidence. Industry compliance standards
Typical usage ratio
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4. Dye Intermediate for Liquid Crystal Display (LCD) Pigment SynthesisIn the electronic materials industry, downstream manufacturers employ this compound for making monoazo and disazo dye intermediates, critical to high-purity pigment pastes for LCD panel color filters. Control of nitro group orientation within the molecule ensures sharp absorption bands and thermal endurance required for modern display technologies, with production lines maintaining full traceability to meet electronic grade standards. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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Inside our production plants, we notice subtle differences batch by batch—a color tone, a hint in particle size—signs only someone hands-on in chemical manufacturing can spot. Years of running reactors and monitoring filtration have ingrained in us just how critical it is to achieve homogeneity in 3,4-dinitrobenzoic acid, not only for lab-scale applications but for scale-up in full industrial processes. With this compound, any small fluctuation can disrupt downstream synthetic efficiency. Our quality control teams conduct rigorous purification to meet stringent purity requirements, letting us consistently deliver a product trusted by custom synthesis and formulation laboratories around the world.
We have lived through the challenges of producing 3,4-dinitrobenzoic acid, known among chemists as a versatile building block, especially because the nitration at both meta and para positions introduces unique electron withdrawing effects. The chemical formula sits at C7H4N2O6, and true to its form, the pale yellow crystalline powder demands both precision and care during production. We keep moisture content low because a slight increase can diminish storage life or complicate solution preparation. Our typical purity ranges above 99%, checked by HPLC and melting point validation. Every specification is built from necessity. Low metallic impurities, minimal residual solvents, and controlled particle size all support suitability for pharmaceutical intermediates and specialty polymers—the two main markets drawing on our consistent output.
In the field, formulators and process chemists come back to us directly, asking for specific sieved fractions of 3,4-dinitrobenzoic acid. Thin-layer chromatography labs demand a particular granularity, while dye and pigment manufacturers prefer denser, larger grains to facilitate easier weighing and handling. Many active pharmaceutical ingredient (API) research groups call out our batch documentation, which traces each lot from raw materials through to drying and final QA. For these customers, product lifecycle matters, not just analytical figures.
In discussion with several custom synthesis groups, it became clear that failing to control ortho-nitration byproducts in 3,4-dinitrobenzoic acid skews outcomes for their downstream benzimidazole and benzotriazole syntheses. We measure our success in those cases where they report fewer side reactions and cleaner reaction profiles thanks to how we cut down contaminant levels. The details only matter in practice, when it means the researcher can move from lab batch to kilo lab without reoptimizing protocols.
Producers regularly compare 3,4-dinitrobenzoic acid to its 2,4- and 2,5- isomers, and we’re no different—we have run all three on the same lines. The molecular backbone remains constant across these isomers, yet the physical behaviors diverge. We observe that 3,4- stands out for its increased acid strength, derived from the synergistic placement of the nitro groups. Our experience tells us it displays greater crystallinity and a sharper melting point than the other isomers, reducing the risk of cross-contamination in downstream transformations.
Because we also manufacture the 2,4- isomer, we can say with certainty that its more labile nitro group sometimes triggers unwanted side reactions, especially in multi-step syntheses. In pigment production lines, the 3,4- isomer stays more robust during high-heat processing. We’ve had customers return to 3,4-DNBA after trying 2,5-DNBA in high-performance dyes, reporting more consistent yields and fewer processing interruptions.
The process to obtain high-purity 3,4-dinitrobenzoic acid is far from simple. It requires precision in temperature control, reagent management, and waste treatment. In more than one campaign, we observed that minor temperature overshoots during nitration led to persistent formation of mono-nitrated intermediates. Frequent sampling and continuous adjustment during reactor charging have become the norm to minimize these effects. Over the years, adopting improved agitation and calibrated acid addition devices cut our impurity loads and improved batch-to-batch reproducibility.
Scaling is another constant challenge. Processing at the kilo level, heat dissipation is under control, but at larger scales, localized hot spots can form, risking formation of tars or decomposed byproducts. To address this, we changed over from traditional batch reactors to semi-continuous flow reactors for several high-volume contracts. This move improved yields and simplified post-processing filtration, which meant increased throughput and lower downtime for line cleaning. We keep data logs on every run, so each step forward is based on actual production data, not assumptions.
Waste management matters just as much as product purity. Nitration reactions generate substantial acidic and nitrogenous waste, which we treat in dedicated neutralization units. In the past, inconsistent neutralization created hidden hazards and compliance issues. With new in-line pH monitors tied to automatic dosing, we catch anomalies the moment they occur. This reduces our environmental footprint and preserves clean operations.
In conversation with longtime partners, we’ve tracked how demand for 3,4-dinitrobenzoic acid shifts as end-use applications change. A decade ago, pigment and photographic chemistry dominated the market. In the past five years, development of specialty polymers and medicinal intermediates reshaped the volume and grade requirements we receive. More research-driven firms request custom sizing and increased purity assurance. Traceability documentation grew from being a value-add to an expectation.
Researchers entering new areas, particularly in materials science and pharmaceutical building blocks, seek flexibility—ordering 3,4-dinitrobenzoic acid in varying batch sizes or with extra documentation to support regulatory filings. These changes push us to refine packaging options: smaller lots in amber glass for sensitive labs, bulk fiber drums for pilot plants. Each adjustment stems from direct client feedback, not generic market trends.
Anyone working close to 3,4-dinitrobenzoic acid knows its hazards differ from those of common commodity acids. The double nitration increases the level of oxidative energy stored within its structure, which calls for controlled storage, consistent moisture management, and strict operator procedures. We train our line staff thoroughly, running safety drills for spill response and emergency shutdowns. In more than one case, early intervention prevented escalation during handling—those lessons stick.
For clients, we emphasize both chemical and practical handling risks. Some customers initially overlook the dusting potential of fine powders during weighing. Having learned this ourselves, we switched standard delivery to granular grades, reducing both airborne particulates and unnecessary product loss. Many research groups value this practical adjustment as much as any certification.
Disposal practices are another frequent question—labs must comply with evolving environmental standards, and every end-user has unique local requirements. We provide clear guidance based on our operating experience, sharing insights about neutralization and dilution methods that ensure safe, efficient waste handling without overcomplicating compliance.
Manufacturers of 3,4-dinitrobenzoic acid have seen regulations grow tighter each year, especially concerning workplace exposures and the transport of nitrated aromatics. We keep up by implementing closed handling during packing and investing in filtration and air exchange to reduce operator exposure. Our staff participates in ongoing training for new regulatory shifts, ensuring our practices meet—and often outpace—all local and international standards.
We also maintain transparent batch records tied to each shipment, enabling partners to trace every key processing variable. This traceability helps R&D and quality teams identify sources of any flagged variance quickly, streamlining product recalls and investigations. Instead of risking a recall due to incomplete GMP documentation, our customers know they receive a batch report for every order, supporting both internal requirements and those from external auditors.
Many innovative polymer and pharmaceutical projects depend on the distinct electronic effects that 3,4-dinitrobenzoic acid introduces during synthesis. In our discussions with academic and commercial teams, we’ve heard that minor lot-to-lot variability—even in color—sometimes signaled significant performance differences in final products. This pushed us to revisit crystallization, introducing fine-tuned temperature ramps and better agitation controls. The result: batches that remain nearly identical month after month.
Feedback from R&D partners shapes our next steps. Some have requested additional analytical data: NMR, FTIR spectra, or residual palladium checks, depending on the intended application. By offering these analyses as part of the standard battery of checks, we support upfront feasibility studies and downstream process automation. Hearing directly from researchers facing failed syntheses due to subpar starting materials underscores why thoroughness at the source pays dividends in the lab.
3,4-Dinitrobenzoic acid serves as a foundation for complex heterocycle synthesis, especially in medicinal chemistry. In our own work with external partners, we have seen how this molecule’s unique structure facilitates directed ortho-metalation and subsequent ring-closure reactions, essential to developing lead compounds in several therapeutic classes. The reliability of every lot ensures researchers avoid unnecessary troubleshooting and keep timelines predictable when moving through discovery and scale-up.
When acting as a supplier for pilot programs exploring antiviral scaffolds or oncology candidate compounds, we encounter demand not just for higher purity, but also for expanded impurity profiling. Teams approach us for isolated samples of process side-products, used internally for toxicological risk assessments and synthetic troubleshooting. As a result, our labs have modified purification trains on request, delivering small side-stream batches that assist in de-risking the drug development pipeline.
We maintain frequent contact with process engineers at client sites, reviewing the real-world performance of 3,4-dinitrobenzoic acid after delivery. These conversations reveal where bottlenecks occur, whether related to solubility in a specific solvent, rate of dissolution under manufacturing conditions, or residue in process equipment. Each technical exchange sharpens our understanding and leads to direct process adjustments—better drying procedures, alternative sieving, or tighter packaging protocols that reflect both our experience and our clients’ operational realities.
Peer manufacturers sometimes explore efficiencies or request collaboration to resolve shared industry hurdles, such as minimizing energetic waste streams or improving crystal morphology for tougher applications. These exchanges lead to long-term improvements, not just for one company’s bottom line but on a sector-wide scale. Improvements become codified in our protocols, so that every new batch benefits from the practical wisdom accumulated across thousands of production hours and dozens of client feedback sessions.
As research into energetic polymers, high-performance pigments, and API intermediates expands, we see 3,4-dinitrobenzoic acid cementing its place as a cornerstone molecule across several advanced fields. Increased regulatory oversight—especially regarding nitroaromatics—means that manufacturers have to meet new documentation standards, provide cleaner analytical profiles, and innovate in waste reduction and energy usage. We anticipate broader adoption of process intensification and more robust real-time analytics in synthesis and purification lines, technologies we already deploy to improve both yield and safety.
Once, suppliers only needed to deliver a product that ‘passed’ a minimum regulatory bar. The modern environment demands traceability, rigorous analysis, and the capacity to offer technical support for very specific application needs. Our ongoing commitment rests in making whatever adjustments are required—no matter how small—to help our partners maintain competitive advantage through quality and reliability. Every team member, from lab technician to plant operator, sees their efforts borne out in the minimal client issues reported and the loyalty of our returning customers.
Daily life within our team means iterative improvement. Operators fine-tune dryer temperature settings to get reproducible crystal sizes. Analysts double-check spectral data to confirm subtle impurities remain within specifications. Commercial teams relay very specific needs from partners, passing them straight to production, bypassing the kind of generic communication that clouds requirements. Every feedback session informs the next production campaign, closing the loop between manufacturer and end-user, a connection that defines the ongoing excellence of our 3,4-dinitrobenzoic acid.
This approach—rooted in hands-on experience and maintained through every link in the chain—gives us confidence that researchers, industrial chemists, and end-users achieve the best results in their work. Product byproduct control, scalability, effective risk management, and responsive technical support remain the pillars of our production philosophy, all in service to an industry that values both tradition and innovation. Whether researchers are launching a new synthetic approach or refining a flagship production process, our experience producing 3,4-dinitrobenzoic acid translates into measurable, everyday reliability.