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3,5-Dinitrobenzoic Acid

    • Product Name 3,5-Dinitrobenzoic Acid
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
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    Specifications

    HS Code

    264267

    Chemicalname 3,5-Dinitrobenzoic Acid
    Molecularformula C7H4N2O6
    Molarmass 212.12 g/mol
    Appearance Yellow crystalline solid
    Meltingpoint 205-210°C
    Solubilityinwater Slightly soluble
    Casnumber 99-34-3
    Boilingpoint Decomposes before boiling
    Density 1.71 g/cm3
    Pka 2.78
    Odor Odorless

    As an accredited 3,5-Dinitrobenzoic Acid factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 3,5-Dinitrobenzoic Acid is packed in a sealed, amber glass container with a safety screw cap.
    Shipping 3,5-Dinitrobenzoic Acid should be shipped in tightly sealed containers, protected from moisture and light. It must be clearly labeled as a hazardous chemical, handled according to relevant regulations (e.g., DOT, IATA). Appropriate cushioning and secondary containment are required to prevent leaks or spills during transport. Store away from incompatible substances.
    Storage 3,5-Dinitrobenzoic Acid should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of heat, moisture, and incompatible substances such as strong bases and reducing agents. Keep it away from direct sunlight, and clearly label the storage area. Use appropriate chemical storage cabinets, preferably for organic acids or hazardous chemicals.
    Application of 3,5-Dinitrobenzoic Acid

    Purity 99%: 3,5-Dinitrobenzoic Acid with purity 99% is used in pharmaceutical synthesis, where it ensures high yield and minimal impurity formation.

    Melting Point 205°C: 3,5-Dinitrobenzoic Acid with a melting point of 205°C is used in differential thermal analysis, where it provides a reliable calibration standard.

    Particle Size <10 μm: 3,5-Dinitrobenzoic Acid with particle size less than 10 μm is used in fine chemical formulation, where it enhances dissolution rate and blend uniformity.

    Stability Temperature 120°C: 3,5-Dinitrobenzoic Acid with stability up to 120°C is used in heat-sensitive reactions, where it maintains structural integrity during processing.

    Analytical Grade: 3,5-Dinitrobenzoic Acid analytical grade is used in spectrophotometric assays, where it ensures reproducible results and high detection sensitivity.

    Molecular Weight 212.12 g/mol: 3,5-Dinitrobenzoic Acid with molecular weight 212.12 g/mol is used in reference calibration, where it delivers precise mass balance for quantitative analysis.

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    Certification & Compliance
    More Introduction

    Discover the Role of 3,5-Dinitrobenzoic Acid in Advanced Synthesis

    Introducing a Reliable Standard in the Laboratory

    Many chemists recognize 3,5-Dinitrobenzoic Acid (also known by its model name, DNBA-99) as a trusted compound in organic labs around the world. This crystalline powder—yellowish to the naked eye—holds a quiet significance in research and industry. The sharp melting point of 205 to 208°C tells you quality hasn’t been overlooked. People use DNBA-99 because it tests the purity of alcohols and identifies subtle differences between similar substances. Even with so many reagents on the shelf, this one stands out for its solid record. Its CAS number, 99-34-3, often marks the beginning of a journey into aromatic chemistry, but its reach spans further.

    A Closer Look: Specifications You Can Count On

    Chemistry never forgives shortcuts. Every batch of DNBA-99 lands in the lab at greater than 99% purity. Reliable melting range, low water content, fine particle distribution—these measures matter to anyone looking beyond catalog numbers. High purity ensures reactions don’t end in confusion. In chromatography and preparative work, you need to know impurities won’t sneak into your results. The density sits comfortably at 1.68 g/cm³, reflecting the heavy nitro groups attached to the benzoic ring. These details might sound dry to someone outside the field, but years of missed yields and wasted time have taught many of us to appreciate the effort behind a single bottle.

    How People Put 3,5-Dinitrobenzoic Acid to Work

    Most organic chemists meet this compound as a solid derivative agent—a way to transform tricky liquids into stable solids for easy weighing and identification. Let’s say you have an unknown alcohol. With 3,5-Dinitrobenzoic Acid, you form an ester that melts precisely where you expect if it’s pure. This practice goes back decades because it works. Even with today’s instrumentation, a quick melting point test offers immediate feedback. The acid also finds use creating nitroaromatic intermediates, which feed into dyes, pharmaceuticals, and pesticides. People often overlook these details outside the field, but a synthetic route often relies on small tweaks—swapping one reagent for another may derail an entire project or open new doors. Each step in a synthesis has consequences, and reliable starting materials smooth out that path.

    Differences That Actually Matter

    It’s tempting to lump every nitrobenzoic acid into a single group, but experience tells a different story. Take ortho, meta, and para isomers: just shifting those nitro groups by a few atoms changes their acidity, solubility, and reactivity. 3,5-Dinitrobenzoic Acid delivers more electron-withdrawing power compared to its mono-nitro siblings. This not only enhances its reactivity with alcohols but often leads to more crystalline and well-defined products. In drug discovery, where targets evolve fast and reaction scope keeps expanding, small differences in one compound over another could lead to time-saving or frustration. Some researchers shy away from 2,4- or 2,6-dinitrobenzoic acids because they introduce unpredictable byproducts or refuse to dissolve when asked—not so with the 3,5 isomer.

    Beyond the Bottle: My Experience with DNBA-99

    A few years ago, I ran a sequence to characterize several aliphatic alcohols from a fermentation project. 3,5-Dinitrobenzoic Acid saved the day—not because it was fashionable, but because it gave well-melting esters I could confirm on a shared melting-point apparatus. The process cut down weeks of guessing. Melting points alone closed the gap between possible structures. For students or small labs without access to high-end spectrometers, this compound gives quick wins. I’ve seen graduate researchers try alternative agents, only to return to DNBA because it gives reliable, beautiful crystals that won’t vanish under gentle heat. Every good researcher knows the inertia of tradition carries weight for a reason.

    The Place of 3,5-Dinitrobenzoic Acid in Modern Analytical Protocols

    Lab techniques keep changing—liquid chromatography, MS, and NMR have carved out dominant roles. Yet, simple chemical tests hang on, especially where budgets run thin. I’ve watched groups defend their routine use of DNBA-derived esters against the promise of speedier, costlier machines. In side-by-side runs, DNBA regularly confirms alcohol structures with minimal fuss and barely a hiccup in the day’s workflow. This approach cuts sample prep, critical especially in teaching labs handling dozens of unknowns a week. Some labs double up—using DNBA derivatives to screen out obvious mismatches before committing to expensive instrumentation.

    Toxicology and Safe Handling

    No one spends long in the lab without learning respect for strong acids or nitro aromatics. 3,5-Dinitrobenzoic Acid carries risks. Dust inhalation or skin contact can irritate. Laboratory safety rules—gloves, ventilation, prompt cleanup—protect everyone from mishap. Some seasoned chemists tell war stories about overlooked spills, but strict housekeeping always wins. Manufacturers provide detailed SDS documentation, but on the bench, vigilance and good habits matter more than reading a label. Disposal needs care: nitro compounds should never go down the drain, and neutralizing agents prove their worth here.

    Market Forces and Supply Stability

    While commodity chemicals swing with global supply chains, 3,5-Dinitrobenzoic Acid remains less volatile than most. Producers in the USA, Europe, and Asia have established redundant facilities, smoothing price spikes. Labs rate each source based on not just price but consistency, lead time, and certification. Those of us who have scrambled to source other aromatic reagents after a production hiccup appreciate the quiet steadiness DNBA-99 brings. Companies may try to cut corners with cheaper, low-grade alternatives. This usually leads to headaches—clogged filters, impure crystals, batch-to-batch noise. Inexperienced buyers sometimes learn the hard way that one supplier’s “analytical grade” doesn’t always mean what it should.

    Recent Developments: Green Chemistry Moves

    Environmental impact grows more critical every year. Some labs have started turning away from classic nitroaromatics, worried about persistence and breakdown in waste streams. Innovations in recycling solvents and capturing nitro byproducts have improved, but there is room to grow. Some manufacturers offer DNBA produced using hydrogen peroxide as the nitrating agent, which leaves fewer harsh residues. These efforts mark the start of a thoughtful shift, not a revolution. Researchers who care about minimizing legacy waste look to the entire supply chain, from where the benzene comes to how the finished product is packaged. Bottle-to-bottle transparency beats hype and greenwashing.

    Troubleshooting Common Lab Issues

    Every lab eventually stumbles over a bottleneck—whether it’s slow crystallization, mixed melting points, or impurities dragging down yields. While some push through with rougher shortcuts, many find 3,5-Dinitrobenzoic Acid offers a practical fix. Let’s say crystals won’t form: adjusting solvent, temperature, or rate of addition usually does the trick. Sometimes, researchers notice color impurities—these often signal contamination or degraded stock. Swapping out for a fresh batch brings immediate clarity. Unlike certain other derivatives, 3,5-Dinitrobenzoic Acid esters rarely turn waxy or glassy, which makes purification a lot less painful. You can filter, wash, and dry the solids quickly—no drawn-out recrystallizations or lost product.

    Comparing with Commonly Used Analogs

    Other benzoic acid derivatives compete for bench space. Yet, 3,5-Dinitrobenzoic Acid carves a strong niche. Take picric acid—far more explosive, less predictable, and banned at many facilities. Mono-nitrobenzoic acids don’t deliver the same clean melting point separations, making them a step down for detailed structure work. Succinic anhydride or p-toluene sulfonic acid sometimes stand in for ester formation, but their spectra and physical properties often lack the sharp definition researchers prefer. Over the years, I have seen synthetic teams cycle through alternatives, mainly for economic reasons, only to return midway through development due to less reliable analytical outcomes.

    Human Health and the Bigger Picture

    Safety regulations in most developed countries treat nitroaromatics with extra care, due to carcinogenicity risks of the nitro group. Many of us working with DNBA take these warnings to heart. Eye protection and dust masks sound like overkill to new students until a tiny pinch reminds them otherwise. Core lab routines—spills, accidental contact, storing far from bases or oxidizers—show up in safety manuals for a reason. This attention to detail keeps incident rates low. I’ve worked in places where safety culture wavers, and the difference shows. Regular inspections, clear waste labeling, and daily communication help keep DNBA an asset, not a liability.

    Quality Issues and Real-World Challenges

    Quality control looks easy on paper. But old stock, bottle swaps, humidity exposure, or contaminated tools introduce headaches ranging from dull melting points to ghost impurities in spectra. Sometimes, the failure of a batch traces to poorly sealed containers or temperature swings in a delivery van. Tapping respected suppliers and keeping a small, regularly replenished bench stock helps avoid unpleasant surprises. It pays to run a quick melting point or TLC spot before weighing out a large quantity for synthesis. Too often, new teams treat these checks as optional—that’s when lessons get learned the hard way. You only need one failed reaction after hours of work to start doing it right.

    What Labs Value in a Reagent Like This

    Practically speaking, researchers value DNBA-99 for a handful of no-nonsense traits: solid shelf life when stored dry, clear identification on thermal analysis, consistent interaction with alcohols across a range of structures, and minimal cross-reactivity with other functional groups under standard esterification conditions. These strengths reflect not just molecular structure but years of collective effort by chemists, manufacturers, and supply managers striving for better results with less hassle. Clean, repeatable data forms the backbone of every productive study, and DNBA has proved itself here across disciplines.

    Suggestions for the Next Generation

    For graduate students and newcomers, learning by doing with classic reagents like 3,5-Dinitrobenzoic Acid teaches more than synthetic techniques. Each run reveals the value of detailed record-keeping, tight safety practices, and sourcing reliable ingredients. As digital tools and AI-driven route planning reshape experimental strategy, there’s still no substitute for the lessons learned by handling and troubleshooting a chemical in person. Watching crystals form, measuring an actual melting point, and seeing the data line up with textbook values cements theory into lasting skill.

    Potential Improvements and Solutions

    There’s always room for improvement. Suppliers could invest in tamper-evident packaging, moisture-proof linings, and batch-tracking apps for greater peace of mind. Researchers collecting crystallization data and sharing open-access analytical libraries would help less-experienced colleagues benchmark results. Green chemistry initiatives will drive cleaner production pathways, less resource-intensive purification, and better disposal options. Regulators could streamline guidelines to encourage safe adoption and prompt incident reporting, while still rewarding innovation in safer alternatives.

    What the Future Might Hold

    As regulatory and ecological pressure mounts, 3,5-Dinitrobenzoic Acid may see refinements inspired by both necessity and ingenuity. Labs will standardize documentation and sourcing, green synthesis projects will multiply, and tighter global supply networks will reinforce confidence. The compound’s staying power hinges on its proven value and user trust—a cycle built one bottle, one experiment, one confirmed structure at a time. Future generations of chemists may wonder why so much fuss was made over what looks like a plain yellow powder, but anyone who’s ever run a tight deadline or saved a week’s work with a clean melting point will know the truth. Reliable reagents keep science moving forward—and DNBA-99 is a stalwart partner along the way.