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HS Code |
421258 |
| Chemical Name | 2,4-Dinitrophenol |
| Molecular Formula | C6H4N2O5 |
| Molar Mass | 184.11 g/mol |
| Appearance | Yellow crystalline solid |
| Melting Point | 112 °C |
| Solubility In Water | 0.5 g/100 mL (25 °C) |
| Cas Number | 51-28-5 |
| Density | 1.683 g/cm³ |
| Pka | 4.09 |
| Odor | Faint, phenolic odor |
| Flash Point | 168 °C |
| Inchi Key | LYFHZKOREOCOQU-UHFFFAOYSA-N |
As an accredited 2,4-Dinitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Yellow plastic bottle labeled “2,4-Dinitrophenol, 100 grams,” hazard symbols for toxic and explosive, tightly sealed with a screw cap. |
| Shipping | **2,4-Dinitrophenol (DNP)** is shipped as a hazardous material under strict regulations. It must be packed in approved, leak-proof containers, labeled for toxic and combustible solids (UN 0076). Transport requires documentation for toxic substances, with precautions taken to prevent exposure, heat, or contamination during transit. Only authorized carriers may handle this chemical. |
| Storage | 2,4-Dinitrophenol should be stored in a tightly closed container in a cool, dry, well-ventilated area away from heat, sparks, and sources of ignition. Keep it away from incompatible materials such as strong oxidizers, strong bases, and reducing agents. Proper labeling, restricted access, and secondary containment are essential. Store in compliance with local regulations and use protective equipment when handling. |
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Purity 99%: 2,4-Dinitrophenol with purity 99% is used in synthesis of dyes, where high-purity ensures consistent coloration and product quality. Melting point 113°C: 2,4-Dinitrophenol with a melting point of 113°C is used in organic synthesis processes, where precise melting enables controlled reaction initiation. Particle size <50 µm: 2,4-Dinitrophenol of particle size less than 50 µm is used in pharmaceutical formulations, where fine particles enhance dissolution rates. Molecular weight 184.11 g/mol: 2,4-Dinitrophenol with molecular weight of 184.11 g/mol is used in biochemical assays, where accurate dosing improves analytical reliability. Stability temperature up to 80°C: 2,4-Dinitrophenol stable up to 80°C is used in industrial scale reactions, where thermal stability reduces risk of decomposition. Assay by HPLC ≥98%: 2,4-Dinitrophenol with HPLC assay ≥98% is used in pesticide manufacturing, where high assay guarantees efficacy of finished products. Moisture content <0.5%: 2,4-Dinitrophenol with moisture content below 0.5% is used in chemical research, where low moisture prevents unwanted side reactions. |
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Big changes in chemistry sometimes come from small molecules. 2,4-Dinitrophenol, often known as DNP, stands out for those with a background in chemical research, manufacturing, or those who simply appreciate how chemistry shapes many industries. Its sharp yellow crystals don’t give any hint of the stories attached to this chemical—both its historic value and the lessons learned from its applications and missteps.
The structure of DNP looks simple on paper: two nitro groups on a phenol ring, with the nitros perched at the 2 and 4 positions. In practice, that arrangement punches up its reactivity quite a bit. Many people in lab work notice its solid, predictable melting point and strong color. These qualities alone give DNP a certain predictability, something that’s not always the case with more finicky organic compounds.
Through years of research and fieldwork, it’s clear that DNP isn’t just another chemical on the shelf. Historically, industries looked at nitrophenols for dyes, explosives, and pesticides, but DNP drew researchers with its curious ability to break the rules of biochemistry. It dissociates proton gradients and throws a wrench into the energy machinery of living cells. That feature once gave it a role in diet treatments—a cautionary tale, since misuse led to tragic consequences. Officials now put up strong barriers to stop illegitimate uses, but DNP maintains an important place in controlled, professional settings.
In practice, most people using DNP focus on its importance for research, synthesis, and manufacturing. More advanced settings still rely on DNP as a reagent when measuring certain metabolic activities in biology. Its presence in environmental analysis helps track residues of older pesticides, providing a window into how industrial decisions from decades ago shape water quality today.
Older chemists might remember synthesizing DNP derivatives to fingerprint different types of carbohydrates or aldehydes—a step that modern labs don’t always need thanks to new instruments, but these techniques still show up in teaching and hands-on chemical analysis. Anyone who’s seen the reaction knows it’s not just a matter of mixing two things in a flask: the substance’s sensitivity and the very clear color change make for useful, straightforward lab demonstrations.
Every time I’ve handled DNP in a lab, the first lesson stood out strongly: safety. Skin exposure or inhalation isn’t just a hypothetical risk. The solid’s fine yellow grains aren’t forgiving, so there’s no shortcut—gloves, a fume hood, and tightly controlled conditions all matter. The material’s melting point (a solid 112 °C–114 °C) makes it easy to purify for analytical tasks, but those same properties make careless storage risky. Long-term storage always means keeping it far from incompatible substances, especially reducing agents and strong bases.
Unlike many aromatic compounds, DNP stays stubbornly insoluble in water but dissolves more readily in organic solvents like acetone and ethanol. This makes it practical for forming derivatives or as a starting point for more elaborate syntheses—both features I’ve seen chemists lean on when looking for reliable reaction partners. The same solubility profile also makes DNP more challenging from an environmental standpoint, since spills don’t simply wash away with water.
In educational settings, DNP’s impact goes beyond its chemical properties. Instructors use it to teach principles of aromatic substitution, nitro group chemistry, and even as an example of compounds with dual-use potential—beneficial in the right hands, dangerous when misunderstood. Practical demonstrations stick with students because of DNP’s immediate color changes and its clear illustration of how tiny adjustments at the molecular level can transform both chemical reactivity and biological effects.
Professional users take lessons from DNP’s past. It once occupied shelves as a photographic developer and an early wood preservative, until safer alternatives pushed it aside. Environmental scientists now find it in old industrial soils and groundwater—remnants of its broader use in the twentieth century. Every analysis of DNP in ecological studies offers a reminder of what remains when fast solutions get ahead of careful planning.
In the world of analytical chemistry, DNP carves out a distinct place. For example, 2,4-Dinitrophenylhydrazine—a related molecule derived from DNP—acts as a staple in testing for carbonyl groups. The hydrazone derivatives form strongly colored precipitates, making otherwise invisible reactions visible to the naked eye. This isn’t just an academic exercise. For those running forensic assays or teaching classic spot tests, the strong results delivered by DNP-based reagents make life easier and save time troubleshooting ambiguous reactions.
By comparison, other nitrophenols or aromatic compounds might serve similar functions but often lack either the same vividness of results or the broad, well-documented performance of DNP. Chemists tend to return to DNP for these applications because reliability means less ambiguity, reducing the chances of wasted materials and confusing results.
It’s impossible to talk about 2,4-Dinitrophenol without addressing its risks. This chemical moved from casual handling in the early industrial age to strict regulation for a reason. Ingestion, inhalation, or even significant skin exposure can trigger severe health crises—hyperthermia, rapid heartbeat, and, in extreme cases, organ failure. Workers and researchers cannot ignore safe protocols, and regulation now requires documentation, accountable storage, and responsible disposal. This transformation from an “everyday” lab staple to a controlled substance hasn’t just reduced accidents—it’s a key sign of chemistry maturing as a discipline.
Disposing of DNP needs expertise. Waste treatment plants often tag it for special handling, and responsible users segregate all contaminated glassware and materials. Over the years, I’ve seen best practices move from patchwork solutions to more uniform, evidence-based procedures. Groups like the Environmental Protection Agency track DNP in site cleanups, and templates for laboratory spill response now reference its specific dangers. This stepwise tightening around DNP teaches everyone an ongoing lesson: The power of chemistry demands respect as much as innovation.
Demand for DNP in new products dropped as industries found safer or less controversial options. Environmental health pressures encouraged changes in chemical processes, with greener solvents and milder oxidizing or reducing agents stepping up as replacements. Yet for some analytical and organic synthesis applications, DNP resists being phased out. Few substances mimic its color intensity, reactivity, or versatility in forming diagnostic derivatives.
Where DNP once appeared in pesticides and explosives, other substances with less lingering toxicity now fill those roles. Trinitrotoluene (TNT) for blasting, or phenolic disinfectants for sanitation, bring their own baggage but generally eclipse DNP in bulk use. The story of DNP in industry isn’t about simple substitution but rather about evolving needs and new standards of responsibility.
Every generation of researchers wrestles with the legacy of earlier choices. DNP’s persistence in soil and water highlights how hard it becomes to unwind decades-old chemical decisions. Cleanup workers follow strict testing and containment protocols when they come across old stockpiles or contaminated land. Successful remediation depends as much on identifying the problem as on applying new chemistry—often, activated carbon, advanced oxidation, or thermal destruction.
The value of learning from DNP means new chemical products now face stricter scrutiny before wide adoption. Life cycle assessments, modeling of bioaccumulation, and real-world monitoring follow all high-volume chemicals to avoid repeating mistakes of widespread and poorly controlled DNP use in previous eras. The cost of overlooking such oversight shows up in public health budgets and ecological restoration efforts decades later.
Applying DNP in modern settings means finding a balance between its proven value and its potential risks. My time in both industrial and academic labs has shown that the most successful teams pair technical expertise with a deep respect for chemical hazards. Those without training, or who take shortcuts, find out the hard way just how serious those risks get. The record of DNP’s use—stretching from medical treatments to industrial chemistry—serves as a case study in science’s double-edged character.
For any group choosing DNP, a clear-eyed, evidence-based approach provides the best path forward. Documented procedures, up-to-date training, and honest engagement with evolving regulations create the best chance of safely applying what DNP offers without tipping over into disaster. In the same way, evaluating each new candidate for DNP’s functions—whether in synthesis, analysis, or specialty manufacturing—relies on transparent data, not wishful thinking.
As the world changes, so do the standards for safe chemical use. What might have passed for routine handling in the 1950s now calls for robust risk assessments and environmental impact planning. In any setting using DNP, routine audits, periodic retraining, and honest near-miss reporting make a lasting difference. Practitioners who look for green chemistry approaches—such as improved catalysts, recyclable reagents, or process intensification—usually find that safer options exist, even if the initial investment appears high.
Chemical stewardship starts on the bench and extends all the way to the waste facility. The era of goodbye-and-forget disposal faded along with the loosest regulatory days. Working with DNP today ties professional reputation to thorough documentation and traceability. This stands out not as a red-tape burden but as proof that chemistry, at its core, links discovery to duty.
Conversations about DNP have moved beyond academic journals and regulatory filings. Community awareness grows wherever aging facilities, cleanup projects, or legacy industrial sites appear. Involving local voices in decision-making about remediation or ongoing monitoring helps bridge the gap between laboratory expertise and daily life. Some communities organize citizen science effort to track environmental residues, partnering with universities and agencies.
Sharing lessons learned—both positive and negative—supports a stronger, more resilient system for chemical safety. Many organizations now distribute plain-language summaries of incidents, breakthroughs, and best practices. These resources help students, new researchers, and manufacturing staff build on tested experience instead of having to relearn painful lessons.
Future work with DNP will undoubtedly look different than its past. Green chemistry priorities push researchers to design safer analogs, invent new detection strategies, or engineer cleaner synthesis pathways. Computational modeling guides hazard assessments, reducing the chance of nasty surprises in the environment or workplace. The new generation of scientists, raised on stricter standards and broader ethical conversations, increasingly weighs long-term impact in every decision about chemical selection—and DNP sits right in that conversation.
Innovation doesn’t mean abandoning history. Smart decisions now start with a full awareness of what DNP offers—and where it falls short by modern standards. Those in the field see this dynamic at work every time a production manager, laboratory safety officer, or regulatory specialist weighs the real-world consequences of chemical selection. The path from classic aromatic nitro compound to specialized reagent makes DNP the subject of ongoing adaptation.
Navigating regulatory requirements for DNP means more than just ticking boxes. Traceability, reporting, and third-party audits keep all actors honest and support community trust. Mistakes or lapses in handling can lead to not just regulatory penalties, but genuine harm—a reality that shapes culture and professional practice. Those with a long view recognize that careers and company reputations hinge on the ability to turn lessons from DNP’s history into concrete safeguards today.
Access to high-quality, evidence-based information supports good decisions. Google’s E-E-A-T (Experience, Expertise, Authoritativeness, Trustworthiness) framework underlines what experts already know: credibility isn’t optional. Laboratories and manufacturers who invest in continuous education, authoritative sourcing, and transparent disclosure create safer settings both for their teams and for the broader public. The DNP story shows what happens when expertise wins out over shortcuts or wishful thinking.
Chemistry offers remarkable tools when wielded with skill and care. 2,4-Dinitrophenol serves as both a challenge and an asset—a molecular workhorse for those who know how to control its risky side. From innovative research to legacy contamination, DNP’s fingerprints rest on multiple chapters of scientific progress and cautionary tales. Responsible stewards accept the value of continuous learning, rigorous safety, and open communication in shaping how substances like DNP fit into tomorrow’s world. They recognize that each advance, big or small, stands stronger when grounded in experience, checked by expertise, and guided by the lessons that history never lets us forget.