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2,4,6-Trinitrophenol (Picric Acid)

    • Product Name 2,4,6-Trinitrophenol (Picric Acid)
    • Alias Picric Acid
    • Einecs 201-865-9
    • 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

    263437

    Chemical Name 2,4,6-Trinitrophenol
    Common Name Picric Acid
    Molecular Formula C6H3N3O7
    Molar Mass 229.10 g/mol
    Cas Number 88-89-1
    Appearance Yellow crystalline solid
    Melting Point 122.5 °C
    Boiling Point 300 °C (decomposes)
    Density 1.763 g/cm³
    Solubility In Water 1.4 g/100 mL (20 °C)
    Odor Odorless or faintly bitter
    Hazard Class Explosive, Toxic

    As an accredited 2,4,6-Trinitrophenol (Picric Acid) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 500g amber glass bottle labeled "2,4,6-Trinitrophenol (Picric Acid)," featuring hazard symbols, tightly sealed, and cushioned in protective packaging.
    Shipping 2,4,6-Trinitrophenol (Picric Acid) must be shipped as a hazardous material under strict regulations. It should be packaged in tightly sealed containers, kept moist to prevent explosion risk, and labeled as explosive (UN 0154). Transport requires compliance with ADR, IATA, and IMDG codes, and only qualified personnel should handle shipping.
    Storage 2,4,6-Trinitrophenol (Picric Acid) should be stored in tightly sealed containers away from heat, sparks, and open flames in a cool, dry, and well-ventilated area. Store separately from incompatible substances, especially metals and reducing agents, to prevent explosive reactions. Avoid friction, shock, or contaminants. Picric acid must be kept moist (with at least 10% water) to minimize explosion risk.
    Application of 2,4,6-Trinitrophenol (Picric Acid)

    Purity 99%: 2,4,6-Trinitrophenol (Picric Acid) with purity 99% is used in analytical chemistry methods, where high-purity ensures reliable and reproducible detection of metal ions.

    Melting Point 122°C: 2,4,6-Trinitrophenol (Picric Acid) with a melting point of 122°C is used in explosives formulation processes, where precise phase transition enhances detonation stability.

    Fine Particle Size <20 μm: 2,4,6-Trinitrophenol (Picric Acid) with fine particle size <20 μm is used in pyrotechnic compositions, where improved dispersibility yields uniform combustion rates.

    Stability Temperature up to 150°C: 2,4,6-Trinitrophenol (Picric Acid) with stability temperature up to 150°C is used in propellant manufacturing, where thermal stability minimizes decomposition during processing.

    Water Content <0.5%: 2,4,6-Trinitrophenol (Picric Acid) with water content less than 0.5% is used in dye synthesis applications, where low moisture content prevents premature hydrolysis reactions.

    Standard Analytical Grade: 2,4,6-Trinitrophenol (Picric Acid) of standard analytical grade is used in laboratory reagent formulations, where consistent quality ensures accuracy in titrimetric analyses.

    High Solubility Parameter: 2,4,6-Trinitrophenol (Picric Acid) with high solubility parameter is used in protein staining protocols, where enhanced solubility promotes effective colorimetric visualization.

    Crystal Form Monoclinic: 2,4,6-Trinitrophenol (Picric Acid) in monoclinic crystal form is used in metallographic etching, where defined crystal morphology provides sharp delineation of grain boundaries.

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    Certification & Compliance
    More Introduction

    Introducing 2,4,6-Trinitrophenol (Picric Acid): An Old Chemical With Modern Importance

    Few chemicals have a story as remarkable as 2,4,6-Trinitrophenol, better known as picric acid. At first glance, its yellow crystals hide a legacy that spans medicine, industry, and science. I remember my first encounter with it during a college laboratory class. Standing over a beaker, I wondered about its journey from invention to today's many uses. Picric acid’s legacy in explosives may come to mind, but over the years, skilled researchers and professionals have discovered how useful it can be for more peaceful pursuits.

    Physical Profile and Model Specification

    This compound takes shape as bright yellow crystals, insoluble in many organic solvents but very soluble in water and alcohol. In laboratories and industry, standard models offer purity levels reaching upwards of 99 percent, minimizing contamination from substances like chloride, sulfate, or heavy metals. Most bottles arrive with net weights ranging from 100 grams to several kilograms. Proper sealing and packaging matter because once dry, even a tiny spark can set off an unintended reaction. For this reason, picric acid is often kept moist—usually with at least 10 percent water content—lowering explosive risk during handling and storage. My own experience with moisture checks reinforced how essential strict quality control remains; you never want to work with desiccated product by accident.

    Picric Acid in Chemistry and Analytical Science

    Analytical chemists reach for picric acid to identify a wide variety of substances. Its strong acidity means it can form crystalline salts with amines, including many alkaloids. This property made it a staple in drug analysis for decades, as precipitate formation offers a straightforward pathway to identification. Even today, some protocols for testing urea or creatinine in biological fluids rely on picric acid because no simpler alternative matches its specificity and reliability. Students and lab techs learn early on how these distinctive yellow crystals, mixed with carefully measured reagents, reveal clues about biochemical content.

    The dye industry counts on picric acid, too. Its iron-clad reputation for providing a striking, stable yellow hue is hard to match. Woodworkers and textile manufacturers, seeking consistent results without fading or smudging, have turned to picric acid dyes since the nineteenth century. Textile chemists know that the affinity of this compound for protein-based fibers (think silk or wool) provides vibrant, long-lasting tones. Synthetic competitors sometimes offer cheaper options, but few yield the same depth and stability—especially when coloring doesn't tolerate shortcuts.

    Comparisons With Other Nitrated Aromatics

    Picric acid belongs to a family of nitroaromatic compounds. Some might compare it to dinitrophenol or trinitrotoluene (TNT), but key differences set it apart. Picric acid’s acidity supersedes that of TNT, granting it value far beyond simple detonation. TNT, while famous for its explosive power, lacks significant application outside demolition, while picric acid bridges multiple fields—from biological staining to acting as a standard in calorimetry. My own experience with calorimetry demonstrated picric acid’s presence as a reference for measuring the heat released in chemical processes. Its reliable energy output offers a dependable benchmark.

    Industrial users notice differences in melting point and solubility. Picric acid melts at around 122.5°C and dissolves well in hot water, whereas TNT stays solid to higher temperatures and resists solubility. These “personality quirks” mean picric acid adapts better to liquid-phase reactions, dye work, and certain analytical tasks. Dinitrophenols, other famous relatives, present lower explosive risk but also lack the pigmentation power and acid strength.

    A Compound With a Legacy: Uses in Industry and Research

    Metallurgists relied on picric acid-based solutions for decades to etch steel micrographs. Under a light microscope, those distinct etch patterns help reveal phase boundaries and defects, supporting safer bridge and building design. Without such accurate etching, construction quality would take a hit. I recall reading metallurgical case studies where faulty etching failed to pick up minute porosity issues—something a high-purity picric acid solution discovered quickly in a repeat test.

    Histology labs worldwide lean on this compound as a tissue fixative, where it preserves biological samples for years of study. While new fixatives have carved space for themselves in modern pathology, classic Bouin’s solution, which blends picric acid with formaldehyde and acetic acid, still finds defenders among the old guard of technicians. The unrivaled clarity in staining cell structures, especially for muscle tissues, persists as a practical reason for continued use.

    In water analysis, picric acid helps detect trace levels of reducing sugars or protein breakdown products. When environmental scientists measure water quality in rivers or lakes, indicators using picric acid reveal contamination with agricultural runoff or industrial effluents. Despite the rise of advanced instrumentation, many smaller labs appreciate the directness of colorimetric assays where yellow hues serve as a ready visual cue.

    Safety, Handling, and Regulatory Attention

    Anyone who has worked with picric acid knows it deserves respect. In dry form, its shock sensitivity raises real concerns. That legacy—stories of lab fires and industrial accidents—fueled strict regulations on storage and use. Modern suppliers take care to ship the product moistened, with built-in seal checks and tamper indicators on every container. Routine inspections within laboratories or factories, looking for crusting or crystal buildup on bottle threads, are more than bureaucratic; they keep everyone safer. Chemical hygiene plans universally list special protocols for handling trinitrophenol, from flameproof cabinets to grounding equipment against static discharge.

    Regulation brings paperwork and oversight. Environmental authorities also keep a watchful eye given potential toxicity to aquatic life and risks to human health at high exposures. Every professional who spends time near picric acid learns the value of lab coats, gloves, proper waste disposal, and clear labeling. There is no shortcut to safe storage, just as there’s no substitute for rigorous education and training for anyone using or handling this substance.

    Environmental Considerations and Mitigation

    Responsibility for the environment matters more now than ever. Picric acid’s potential impact on waterways or wildlife can’t be ignored. Accidental spills historically caused fish kills and long-term contamination, especially downwind from explosives factories during the early 1900s. Today, researchers and manufacturers work to limit releases. Companies install specialized waste treatment systems, using activated carbon and advanced filtration, catching and neutralizing residues before they reach public water. Academic training often includes hands-on waste management exercises so future chemists grow familiar with environmentally sound practices instead of learning from avoidable mistakes.

    Regulators worldwide have stepped up expectations on reporting and remediation. Safety data sheets and environmental regulations now call for closed-loop processing and prompt cleanup of even small leaks. Decision-makers ask for regular audits and updated best practice protocols. These real-world steps go beyond box-checking and help to protect the community.

    Meeting Modern Research and Production Needs

    Modern research and production demand consistency and reliability. Several decades back, batch-to-batch purity fluctuated, which spoiled test results or ruined dye quality. Better purification and quality assurance have changed the picture. Standard analytical methods—chromatography, mass spectrometry, and spectrophotometry—let today’s users check incoming material for trace contamination at parts-per-million levels. As a researcher in grad school, I remember how time-consuming old test kits could get. Now, a few electronic checks can confirm both purity and water content, increasing efficiency and trust in every container.

    The pharmaceutical industry once counted heavily on picric acid for the manufacture of antiseptics and other intermediates, though its role has become less central today. Still, synthetic chemists look at trinitrophenol as a valuable building block for other high-value molecules. In specialty areas—such as forensic science or trace explosive detection—picric acid’s characteristic chemical “signature” comes in useful for swab tests and crime scene analysis. These applications may not grab headlines, but they quietly support public safety and scientific discovery.

    Improving Safety and Efficiency: Ways Forward

    Safer chemistry means changing both habits and technology. In practice, chemical manufacturers continue to innovate packaging and handling. Double-walled bottles, clear water content markings, and robust seals help keep product moist and safely storable. In my experience, digital inventory systems that flag soon-to-expire containers or drops in moisture content add another layer of security. Small investments in training and tech upgrades can prevent major incidents, and many organizations recommend annual or even semi-annual training refreshers.

    Developments in green chemistry suggest a path toward alternatives for applications that historically relied on picric acid. Some modern dyes and fixatives replace trinitrophenol, boasting lower toxicity or simpler waste management. In analytical chemistry, new reagents and automation have reduced reliance on classic color reactions in some cases. Yet, the unique profile of picric acid—clear responses, unambiguous color change, and broad substrate compatibility—means it holds ground in many workflow pipelines. Research teams face the question: Where can safer, greener substitutes step in without sacrificing experimental quality? Collaboration between academic researchers, suppliers, and regulatory experts will shape tomorrow’s answer.

    The Historical Footprint and Ethical Use

    A glance into history books reveals picric acid’s shifting reputation. During wartime, ammunition factories pumped out huge volumes, but peacetime threaded its way through the dye works, laboratories, and clinics. The world learned vital lessons after accidents and environmental incidents, shaping protocols that control everything from bottle labeling to site decommissioning.

    Ethical use takes more than legal compliance. Transparency about risks, open education for end users, and consistent review of new alternatives all figure into responsible stewardship. Laboratories that foster open discussion about chemical risk see better outcomes and safer workplaces. Encouraging a “culture of questioning” also improves innovation, as users identify procedural weaknesses or suggest smarter protocols—sometimes leading to industry-wide improvements.

    Supporting Facts and Solutions To Ongoing Challenges

    Statistics show that even with less use today, trinitrophenol turns up in hundreds of published research protocols each year. Recent environmental monitoring reports highlight why vigilance remains critical: measurable levels in river sediments adjacent to legacy industrial sites persist, decades after production stops. In response, environmental engineers champion targeted cleanup—the use of remediation bacteria, chemical neutralization, and land restoration.

    From a practical perspective, personnel training often makes the biggest difference. Accidents hinge on overlooked basics: dry bottles, mislabeled containers, or poor storage. Periodic safety drills, clear waste separation, and documentation all pay dividends. Sharing real-world case studies, not just textbook scenarios, builds understanding and vigilance. I recall safety seminars run by veteran lab managers; stories of mistakes and near-misses did more than any slide deck to impress the importance of discipline and care.

    Industry and academia also cooperate to phase out noncritical uses of potentially explosive substances. Some universities have set up exchange programs for leftover hazardous chemicals, reducing storage times and the odds of dangerous build-up. Innovative start-ups offer “last-mile” disposal and pickup services, so aging research stocks don’t sit forgotten on a high shelf. Manufacturers continue to invest in greener synthesis routes and better recycling of byproducts, prompted by growing social pressure and tightening regulations.

    Comparing the Experience of Related Compounds

    Working with similar compounds highlights the unique profile of picric acid. Take TNT—standard in demolition, but risky to store near sensitive areas and offering no tie-ins to modern chemical analysis or biological research. Dinitrophenol, once popular for wood preservatives and non-military uses, lost favor after chronic toxicity cases came to light. Picric acid, with its decades-spanning career across science and art, provides a rare blend of chemical utility and analytical precision. This track record brings both responsibility and opportunity.

    Many users remember their first hands-on session with trinitrophenol—a nervousness laced with respect, shaped by careful preparation and oversight. Over time, this respect becomes routine, but never fades. Proper education prepares new generations to balance risk and innovation, ushering in safer products and smarter protocols in every setting from school labs to high-throughput industry.

    Looking Ahead: Responsible Use and Continuous Improvement

    The future of picric acid likely won’t feature new blockbuster uses, but its role as a benchmark and a teaching tool holds steady. Science moves forward through thoughtful evolution, not reckless leaps. As research, regulation, and technology advance, safer practices and greener alternatives will take a greater share of routine work. Knowledge passes from teacher to student, supervisor to trainee, and each reinforces lessons born of both success and failure.

    The legacy of 2,4,6-Trinitrophenol proves that a chemical can outgrow its original purpose and find value in unexpected places. From analytical chemistry and biological staining to industrial dye work, picric acid keeps showing up where clarity and dependability matter most. This reputation rests on more than chemical bonds; it draws on the experience of workers, teachers, and innovators who continue to refine how—and why—we use these powerful compounds safely and responsibly.