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HS Code |
430639 |
| Cas Number | 119-26-6 |
| Molecular Formula | C7H4N2O5 |
| Molar Mass | 196.12 g/mol |
| Appearance | Yellow crystalline powder |
| Melting Point | 211-213 °C |
| Solubility In Water | Slightly soluble |
| Density | 1.68 g/cm³ |
| Pka | 1.47 |
| Pubchem Cid | 8576 |
| Synonyms | 2,4-DNB acid; DNBA; Benzoic acid, 2,4-dinitro- |
As an accredited 2,4-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 2,4-Dinitrobenzoic Acid; labeled with hazard symbols, product details, and safety information. |
| Shipping | **2,4-Dinitrobenzoic Acid** should be shipped in tightly sealed, chemical-resistant containers, clearly labeled with hazard information. It must be protected from moisture and incompatible substances, and transported according to relevant regulations for hazardous chemicals. Ensure packaging prevents leaks and damage, and include appropriate documentation for safe handling and transport. |
| Storage | 2,4-Dinitrobenzoic acid should be stored in a tightly closed container in a cool, dry, well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizing agents and strong bases. Protect it from moisture and direct sunlight. Store it at room temperature and clearly label the container. Wear appropriate personal protective equipment when handling or accessing storage. |
Applications of 2,4-Dinitrobenzoic Acid in Industrial Manufacturing2,4-Dinitrobenzoic acid supports critical transformations and quality controls in various industrial sectors. As a direct manufacturer, we supply to specialized downstream applications requiring precise formulation, batch repeatability, and compliance with demanding regulatory systems. Below, we outline major industrial uses with detailed compliance, usage ratio, process stage, and end-product types. 1. Pharmaceutical Intermediate for API Synthesis2,4-Dinitrobenzoic acid functions as a key intermediate in pharmaceutical manufacturing, particularly in the preparation of active pharmaceutical ingredients (APIs) such as certain antihypertensives and anti-inflammatory drugs. Downstream processors rely on defined purity and consistency to maintain synthetic performance and comply with validated process routes, particularly in nitration and reduction steps. The compound enters the API synthesis via controlled batch reactions, ensuring that trace impurities meet limits established in pharmacopoeias. Finished APIs must satisfy both synthesis quality and strict release specifications, demanding reliable sourcing at scale. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Intermediate in Agricultural Chemical SynthesisIn the agrochemical sector, 2,4-dinitrobenzoic acid acts as a precursor for selective herbicide and pesticide molecules. Formulators employ it in the synthesis of dinitroaniline derivatives and other highly regulated crop protection compounds. Precise reaction monitoring ensures that intermediates meet established residue and toxicity thresholds, supporting both product efficacy and environmental safety throughout the manufacturing line. Production lines require strict traceability from raw material input to formulation filling. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Analytical Reference Material for Chemical TestingRegulatory laboratories and in-house QC facilities use 2,4-dinitrobenzoic acid as a certified reference standard to verify both instrumentation accuracy and method specificity. Its well-defined melting point and spectral characteristics aid calibration in HPLC, GC, and titration systems, forming a reliable benchmark in environmental monitoring, pharmaceutical analysis, and polymer QC. Routine use reduces laboratory batch variability and enhances traceability to national or international standards, increasing confidence in compliance-driven reporting and release procedures. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Dye and Pigment Precursor in Specialty Colorant ProductionManufacturers in the synthetic dye and pigment sector use 2,4-dinitrobenzoic acid as an aromatic substrate for constructing azo and nitro dyes. The compound's nitro substituents enable controlled coupling, providing selectivity in chromophore assembly and contributing to fastness and brilliance in the resulting pigments. High purity and consistent granularity are critical for batch-to-batch reproducibility, particularly in high-sensitivity textile, leather, and specialty ink applications. Production units link precise dosing with automation to minimize shade drift and off-spec outputs. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
5. Reagent for Organic Structure Elucidation in R&DIn chemical research and new molecule development, scientists utilize 2,4-dinitrobenzoic acid as a derivatizing agent for the structural confirmation of amines and alcohols. Its reaction with target functional groups produces crystalline derivatives with sharp melting points, facilitating precise compound identification. Synthetic chemists leverage this property during structure elucidation, compound purity assessment, and in mechanistic studies where purity, reactivity, and clear analytical characteristics are fundamental for publication and patent support. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
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As a manufacturer rooted in decades of chemical synthesis, we know the difference between small variations in compounds can mean a dramatic impact downstream in laboratory and industrial work. Among the aromatic carboxylic acids, 2,4-Dinitrobenzoic acid stands out not simply as another item in our catalog, but as a benchmark for purity and predictable behavior under diverse conditions. Our experience with this molecule stretches across laboratories, pilot plants, and full-scale production, each step reinforcing both its technological importance and its challenges.
C7H4N2O5—those eight atoms hold more than theoretical value. The introduction of two nitro groups in the 2 and 4 positions on the benzoic acid ring creates a precise shift in acidity, electron distribution, and solubility profile. We have witnessed countless researchers come to this compound as a reagent for spot tests in organic synthesis, or as a tool to differentiate amine groups via stable derivatives. Even minor deviations from the required structure, which we avoid using precise analytical monitoring, affect outcomes: yields drop, purity of target molecules suffers, and analytical data can show frustrating noise.
The margin for error narrows further when you face automated workflows, where each batch must behave identically. Our process chemists, working shoulder-to-shoulder with analytical teams, roughed out a manufacturing route tuned not just for high assay, but for crisp batch-to-batch consistency—because users depend on reproducibility far more than glossy spec sheets claim.
Product forms come from specific customer feedback. Our model of 2,4-Dinitrobenzoic acid is a pale yellow crystalline powder, offered mainly in bulk batches starting at 1 kg, but also scaled to fit multi-ton orders as demand emerges in fields like agrochemical intermediates and pharmaceuticals. Melting point checkpoints, handled both in-line via digital melting systems and post-processing by manual review, hold steady between 237°C and 240°C; this gives immediate feedback for batch quality. Some suppliers cut corners with wider melting ranges, but chemists rely on that precision for reliable downstream reactions.
We set moisture limits well below 0.5%, using vacuum ovens and Karl Fischer titration, since even a small amount of residual water skews nitration control and crystallization processes. Iron and other transition metal content stays below 10 ppm, since catalytic residues can ruin certain derivatization reactions. Package integrity directly affects these numbers—a lesson learned years ago when we traced a recurring customer complaint to storage drum linings, since some low-grade containers leach microcontaminants. Switching suppliers and moving to inert liners wiped out the issue, but only after losing production hours and customer faith.
Every person working in our packing section knows the acid’s requirements. Those who have handled 2,4-Dinitrobenzoic acid in a chemistry lab appreciate its ability to react cleanly with primary and secondary amines. For qualitative identification, forming a dinitrobenzamide offers a sharp melting point and distinctive color, which old-school chemists still trust in spot testing. Analytical labs call for the highest possible purity, since even single-digit ppm organic contamination skews HPLC traces and causes tailing—leading to wasted time tracking down phantom peaks.
Bulk customers in dye intermediate production seek the robust aromatic nitro structure, since electron-withdrawing nitro groups offer sites for further reduction or coupling. Our partners in the agricultural sector rely on it to produce certain herbicide molecules, each subject to regulatory scrutiny for trace byproducts. On one occasion, a customer flagged deviations in plant growth regulation, traced to minor differences in impurity profiles. Collaborative review led us to enhance recrystallization protocols and upgrade solvent purification. Such iterative process improvements feed back into our QC program, so the lessons learned become permanent advantages.
Chemists sometimes wonder why we don’t simply use unsubstituted benzoic acid, para-nitrobenzoic acid, or 3,5-dinitrobenzoic acid for similar work. The short answer lies in the fine-tuned electronic effects from the 2,4-nitro substitution pattern. 2,4-Dinitrobenzoic acid demonstrates stronger acid strength than its monosubstituted relatives (pKa shifts lower), direct consequence of the second nitro group’s position. This makes it more reactive, for both analytical derivative formation and as a precursor in more demanding synthetic steps.
Compared to 3,5-dinitrobenzoic acid, which we also manufacture, the 2,4 isomer tends to crystallize more readily and creates derivatives with sharper melting points. In practical terms, this simple spatial rearrangement leads to differences in processability and reproducibility—most noticeable to researchers running multi-step syntheses or ensuring regulatory compliance through distinct impurity fingerprints.
Not every substitution pattern offers that advantage. Some users chasing specific melting points or solubility curves turn back to the 2,4 compound after direct comparison studies. Others recognize the need for both isomers and source them from us side-by-side, precisely because minor structural differences change reaction outcomes that cascade downstream.
Scaling up 2,4-Dinitrobenzoic acid production from grams to kilograms, and then to multi-ton lots, brings out subtle hurdles. Early in our production history, we saw batch-to-batch variation in color and purity during transition from glassware synthesis to stirred reactors. Even with all documentation and controls, unexpected issues emerged: a minor temperature deviation rippled through the nitration stage, leaving more unreacted starting material and off-color product. Adjustments on the fly did not solve the issue—only systematic analysis of mixing, reagent charge rate, and temperature controls at large scale put solutions in place.
A major turning point arrived from investing in continuous monitoring—both process analytics and post-production QA. Instead of using spot sampling, we now employ real-time spectrographic tracking on every production run. Catching subpar batches early improved both the portion of lots meeting our standards and feedback speed to engineering. Downstream, customers quickly noticed fewer deviations in product appearance or chemical behavior. By tightening process sampling, we drove internal reject rates down, saving as much on waste disposal as on raw material costs.
Another lesson surfaced with supply chain interruptions. Nitric acid purity, for example, directly sets the nitro group introduction efficiency. After a supplier shifted to a new purification method, subtle changes arose in reaction exothermicity and side-product levels. Early engagement with that supplier, sharing our in-plant data, allowed joint troubleshooting and adjustments. Subsequent improvement benefited both firms, and we use this as a blueprint for all critical reagent sourcing.
Every person working in our QC lab understands that analytical results don’t stop at specification lines on a page. While we meet all standard assay and impurity requirements, we don’t stop there—historical data analysis helps us spot trends before they become customer issues. Chromatographic fingerprints, tracked lot by lot, reveal any creeping shifts in impurity patterns. That’s important when users require guaranteed absence of certain byproducts for regulatory filings. Only with thorough in-house data, including retention time and peak area consistency, can we stand behind the label on every drum.
We conduct random sampling beyond protocol—double-checking not just the main batch tank, but intermediate storage and transfer lines. Years ago, a stubborn odor problem eluded standard testing. Only after pulling multi-point samples did we isolated a small leak, fixed the source, and added routine checks in the SOP. Over time, customer complaints dropped, confirming the investment in time and staff.
A persistent challenge involves accurate residual solvent determination. Analytical teams use headspace GC, achieving detection limits below 10 ppm for the main solvents involved. Periodic proficiency testing—running blind samples and cross-checking results both internally and with partner labs—keeps both equipment and staff performance sharp. Transparency also opens the door for joint development projects, as in cases where customers bring us unique application requests.
Packing 2,4-Dinitrobenzoic acid goes beyond tossing powder into a drum or bag. Moisture control means nitrogen purging for larger containers and constant humidity monitoring for the storage area. We learned the hard way that even triple-bagging inside inferior drums cannot truly prevent condensation if the warehouse fluctuates. That led to upgraded HVAC and staff training—so no matter the season, product arrives at customer labs in the same pristine state every time.
Transportation regulations classify 2,4-Dinitrobenzoic acid as hazardous, due to the combined presence of nitro groups and aromatic acidity. All staff undergo regular hazmat updates, and logistic partners are chosen for their track record—not price alone. A few times, transport incidents have highlighted gaps in documentation or packaging durability, but each became fodder for new standards and workarounds. By anticipating points of failure, we reduce headaches and liability, both for us and our customers.
Direct feedback from users has long shaped our approach more than any textbook. Some years ago, a customer flagged recurring turbidity in solution tests from a new lot. They attached UV-Vis spectra, which matched a rare byproduct only found in suboptimal crystallization. While most companies might brush off such small impurities, we traced it to a templated cooling step. Adjusting the schedule and communicating this with the customer not only solved the issue, but deepened our working relationship.
Repeat users rely on predictable performance. Basic questions, such as whether a new lot can substitute for the previous batch without rerunning all validation tests, cut to the heart of trust. Lab managers demand certificates of analysis backed by real data access. We often provide fingerprint chromatograms, not just tabs or values. As methods evolve, especially in regulated environments, we field technical queries daily and use these as opportunities to improve—both in product and documentation quality.
Occasionally, we see requests for nonstandard particle sizes or solvent-wet forms, often for specialized derivatization. As production experts, we don’t simply grind down batches. We re-examine crystallization, filtration, and drying, knowing each process change can alter flow properties, solubility, and reactivity. Co-developing custom grades means sharing risk and knowledge, cementing our place as a partner rather than just a supplier.
Manufacturing 2,4-Dinitrobenzoic acid brings environmental responsibility. Waste nitration streams create both acidic and nitro-organic contaminants, strictly regulated in many regions. Over the past decade, we invested heavily in on-site treatment units: neutralization, activated carbon, and advanced oxidation. Staff receive ongoing training in pollution prevention, since a mistake not only endangers our license, but also impacts the broader community.
We maintain internal lot traceability extending to raw material sources. If a new restricted substance list or compliance change arrives, we can quickly certify composition and respond to audits. Experience has shown that proactive documentation wins critical approvals in new markets—a lesson that saved months on several global customer projects.
As regulations tighten on both chemical constituents and downstream applications, continuous reviews of process safety, emission levels, and exposure data become central. Our R&D and safety teams collaborate in updating process risk assessments, bridging our experience on the manufacturing floor with compliance expectations from authorities abroad.
Handling and storing 2,4-Dinitrobenzoic acid on-site calls for basics learned in production: dry storage, sealed containers, and controlled temps to prevent caking or decomposition, since trace water can set off side reactions in humid labs. Lab-scale users benefit from pre-dried aliquots and clear labeling of lot and analysis data. In scaling up, proper dust control and ventilation maintain both worker safety and product quality.
For those conducting derivatization, slow addition and temperature control reduce hazardous exotherms—knowledge born out of years supervising both pilot plant and full-line operations. In recovery from spillage or off-specification events, direct communication with our technical team saves both material and time.
The reason 2,4-Dinitrobenzoic acid continues to anchor laboratories, pilot lines, and industrial syntheses isn’t simple tradition. It offers a unique blend of reactivity, selective derivatization, and unmistakable analytical signatures. For those running critical identification steps, such as amine analysis, or driving high-precision syntheses forward, the quality baseline doesn’t come from self-declaration but from field-tested reliability over thousands of kilogram-lots.
Improvements made along the way stem from open dialogue with users, rooted in shared interest in reliable, safe, sustainable product. By aligning our expertise with evolving expectations, we maintain a product not as a static commodity, but as a crafted solution shaped by real-world feedback and continuous learning. In the crowded world of chemical intermediates, 2,4-Dinitrobenzoic acid stands out through this blend of technical rigor, practical adaptation, and honest transparency—qualities shaped by experience rather than brochure promises.