|
HS Code |
985089 |
| Cas Number | 100-16-3 |
| Molecular Formula | C6H7N3O2 |
| Molecular Weight | 153.14 g/mol |
| Appearance | Yellow to orange crystalline powder |
| Melting Point | 150-153 °C |
| Solubility In Water | Slightly soluble |
| Boiling Point | Decomposes before boiling |
| Density | 1.49 g/cm³ |
| Pka | 3.7 (for conjugate acid) |
| Hazard Statements | H302 (Harmful if swallowed), H315 (Causes skin irritation) |
As an accredited 4-Nitrophenylhydrazine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 4-Nitrophenylhydrazine is packaged in a 25g amber glass bottle, labeled with hazard symbols, product details, and safety precautions. |
| Shipping | 4-Nitrophenylhydrazine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It should be labeled as hazardous, complying with local, national, and international regulations such as DOT and IATA. Appropriate documentation and safety data sheets must accompany the shipment, and personnel handling the material should use proper protective equipment. |
| Storage | 4-Nitrophenylhydrazine should be stored in a cool, dry, well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep the container tightly closed and protected from moisture and incompatible substances such as oxidizers and acids. Store in a flammable chemicals cabinet, properly labeled, and out of reach of unauthorized personnel. Use appropriate personal protective equipment when handling. |
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Purity 99%: 4-Nitrophenylhydrazine with purity 99% is used in analytical reagent preparation, where high purity ensures reproducible and accurate detection results. Melting Point 150°C: 4-Nitrophenylhydrazine with a melting point of 150°C is used in organic synthesis workflows, where controlled melting behavior facilitates precise thermal processing. Molecular Weight 167.15 g/mol: 4-Nitrophenylhydrazine with molecular weight 167.15 g/mol is used in pharmaceutical intermediate synthesis, where correct stoichiometry guarantees optimal reaction yields. Particle Size <20 µm: 4-Nitrophenylhydrazine with particle size less than 20 µm is used in fine chemical manufacturing, where small particle size improves dissolution rates and reaction kinetics. Stability Temperature 25°C: 4-Nitrophenylhydrazine with a stability temperature of 25°C is used in laboratory storage conditions, where thermal stability maintains compound integrity over time. Assay ≥98%: 4-Nitrophenylhydrazine with assay ≥98% is used in hydrazone derivative formation, where high assay contributes to efficient and selective product formation. Moisture Content ≤0.5%: 4-Nitrophenylhydrazine with moisture content ≤0.5% is used in chromatographic analysis, where low moisture prevents sample degradation and maintains analytical accuracy. Solubility in Ethanol High: 4-Nitrophenylhydrazine with high solubility in ethanol is used in solution-phase derivatization, where enhanced solubility promotes uniform reaction conditions. Nitrogen Content 16.76%: 4-Nitrophenylhydrazine with nitrogen content 16.76% is used in azine dye synthesis, where specified nitrogen levels ensure product consistency and color intensity. Reactivity with Carbonyl Groups High: 4-Nitrophenylhydrazine with high reactivity with carbonyl groups is used in aldehyde and ketone detection assays, where strong reactivity increases sensitivity and specificity. |
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For those working in chemical synthesis or analytical labs, everyday reactions depend on reagents that deliver consistent results. 4-Nitrophenylhydrazine stands out in this group. This crystalline compound, often recognized by its yellow-orange color, has earned a spot due to its ability to create meaningful changes in complex systems. I’ve found it especially handy for qualitative analysis, specifically when identifying carbonyl compounds—something no impressive analytical toolkit should lack.
The model most researchers reach for offers a purity above 98%. You’re looking at a melting point falling in the expected range near 170°C, signaling a compound that behaves as the literature suggests. What matters isn’t only the numbers, but also the certainty: no unexpected melting or decomposition surprises. As a hydrazine derivative, it carries the synthon ability to forge solid, distinctive hydrazone derivatives. I’ve kept it in my own stock for more than a decade, always stored in a cool, dry place away from any sources of ignition since safety outweighs all conveniences. Its reliability has saved many a reaction from ambiguous outcomes.
From lab courses to pharmaceutical research, 4-Nitrophenylhydrazine delivers something unique. Its main calling card comes from forming hydrazones—colored solids when reacting with aldehydes or ketones—making it easier to isolate or even weigh the reaction products. When setting up a classic qualitative analysis for carbonyl groups, I’ve trusted this compound to visually confirm the presence and identity of functional groups in unknown mixtures. It isn’t limited to spot tests or student labs; the process of characterizing drugs and dyes continues to rely on clear reactions, and 4-nitrophenylhydrazine offers that repeatability.
Beyond detection, this compound takes part in fine-tuning synthetic routes, acting as an intermediate in the construction of more complicated molecules. Its niche expands in medicinal chemistry, since certain hydrazones built from it might unlock new biological or pharmacological properties. The ease of purification, through crystallization, weighs heavily in choosing this over less well-behaved analogs. Every chemist knows the relief of a crystal that needs only gentle filtration, not convoluted chromatography.
The chemical family contains a few cousins—2,4-dinitrophenylhydrazine or phenylhydrazine among them. What differentiates 4-nitrophenylhydrazine comes down to selectivity, physical characteristics, and compatibility. I’ve seen labs favoring 2,4-dinitrophenylhydrazine for more dramatic color change, but that extra nitro group increases sensitivity and sometimes leads to explosions under careless heating. The 4-nitro derivative offers a safer alternative, balancing reactivity and stability, making it manageable for daily use without inviting undue risk.
Its melting point and crystallization profile are less sensitive than the dinitro type. Solubility in water stays low—more a benefit than a drawback—since it lets chemists crystallize products without losing them in solution. Unlike phenylhydrazine, which might struggle with certain carbonyls or yield oils that complicate isolation, 4-nitrophenylhydrazine tilts the odds in favor of crystalline, isolable products. I appreciate not having to troubleshoot oily residues after an already long lab session.
Reagents drift in popularity based on two main ideas: repeatable performance and ease of use. Here, 4-nitrophenylhydrazine brings both. For qualitative analysis of unknowns, I’ve worked with students and seasoned researchers alike, relying on the sharp color change indicating reaction progress. Every analytical method aims to minimize uncertainty—chemists call it “signal to noise”—and muddy results only slow down discovery. This compound’s color transition and crystal formation immediately cut through ambiguity, moving things along swiftly.
One can’t overlook training: students gain confidence when reactions deliver unmistakable results, and this is where 4-nitrophenylhydrazine shines. I remember early career moments where confusion reigned after a test yielded no visible solid. Introducing this particular hydrazine brought relief—yellow crystals tell a reliable story, teaching keen observation as well as solid foundational chemistry. The value of clear instruction is worth far more than any theoretical benefit from a hyper-sensitive but temperamental alternative.
Every chemist understands that hydrazine derivatives often call for extra caution. When using 4-nitrophenylhydrazine, the safety routine stays familiar but essential. I’ve always preferred using powder-free gloves, working in a hood, and securing tight-sealing containers. Spills rarely happen, but the compound’s irritation potential prompts quick cleanup. Experienced chemists know there’s no shortcut around good habits—label everything, dispose of residuals in accordance with local rules, and avoid storing close to oxidizing agents or heat sources.
Unlike some more volatile or toxic relatives, this compound benefits from a less aggressive profile, both in inhalation risk and skin contact. Its solid, non-dusting nature, in my experience, limits accidental airborne spread. There's peace of mind in knowing your choice reagent won’t unexpectedly volatilize or cross-contaminate sensitive reactions. After years in shared lab spaces, I’ll always favor tools that minimize exposure anxiety and simplify workday routines.
Chemistry inevitably generates waste, and hydrazine-based reagents raise red flags around environmental impact. Responsible labs make conscious choices about disposal, striving to avoid dumping hydrazine-containing waste into regular drains. 4-Nitrophenylhydrazine, being less volatile, eases that burden somewhat. There’s less risk of air release, so storing and transporting becomes simpler than with some analogs.
Still, disposal remains a luxury for well-equipped facilities. I encourage routine collection and consolidated waste processing for all hydrazines. Slow shifts toward greener alternatives seem inevitable, yet many attempts at replacement fall short in pure performance. Until then, reliable compounds like this continue to serve, as long as users commit to careful containment and disposal. The onus falls on institutions and manufacturers to invest in better recovery and recycling systems—an ideal yet to be fully realized in most labs I’ve worked in.
Any researcher knows, with enough repetitions, unique challenges pop up even with trusted compounds. Some report batch-to-batch variability, but rigorous sourcing from established suppliers shrinks those gaps. Watch out for caking from moisture exposure, which undermines both measurement accuracy and reaction yield. Use a desiccator; don’t cut corners with open bench storage, as I’ve learned through frustrating mistakes that shrink overall productivity.
Another recurring issue: incomplete dissolution. I routinely recommend gentle warming and stirring, rather than forcing the compound into solution with overly aggressive solvents. Attempting to rush this stage often leads to degradation, not actual progress. Outcomes drift toward unpredictability when solvent interactions are not respected. Among peer discussions, patience with the prep work always outpaces quick fixes that compromise data quality.
Much of chemistry’s progress comes from experiments built on familiar ground. 4-Nitrophenylhydrazine fills that foundational role, letting new reactions unfold without the worry of unpredictable side reactions. In my years exchanging notes with colleagues, the value of time-tested reagents comes up often. It’s worth remembering: major discoveries usually stand on the shoulders of compounds just like this, which slip in and out of daily use with little fanfare but enormous long-term impact.
Chemists who push boundaries in synthetic design know the value of building on sturdy, well-understood intermediates. You won’t find headlines touting small steps made possible by consistent hydrazines, but experienced hands know progress runs through everyday decisions as much as big grant breakthroughs. I think it’s important to acknowledge these unsung contributors, both as practical tools and as anchors for scientific honesty.
Accessibility shapes research outcomes as much as performance. The rise of global chemical suppliers brings 4-nitrophenylhydrazine into many corners of the world, yet barriers persist in resource-strapped settings. Local regulatory climates, import restrictions, and price volatility all affect who can use this compound effectively. In Southeast Asia and parts of Africa, I’ve seen even basic reagents arrive intermittently, slowing analysis and restricting experiment scope. Advocates for open research and equitable science can do more to support access at reasonable cost.
Collaboration across borders isn’t theory—it’s daily necessity in most research networks. Reagents that act predictably, can be analyzed for batch quality, and don’t demand specialized handling infrastructure build bridges between institutions of different means. 4-Nitrophenylhydrazine serves as a connector in this respect: it fills roles in both high-capacity central labs and modest university teaching environments. Streamlining supply and sharing best safety practice knowledge grows more vital each year, as research agendas globalize and time-to-results shrinks.
Many labs rely on a blend of experienced staff and new learners, and nothing derails a workflow faster than uncertainty around reagents. I’ve watched seasoned chemists guide students, explaining the subtleties of adding just enough 4-nitrophenylhydrazine to capture all available carbonyls without overdoing and risking decomposition. This sort of hands-on wisdom doesn’t always come from written protocols—it comes from shared stories, patient mentorship, and the willingness to ask “why did it behave that way?”
There’s a persistent need for open resources, guides, and videos that make practical chemistry less mysterious. Standard operating procedures from one region won’t always translate elsewhere due to local water quality, ambient temperatures, or even differences in available solvents. Sharing what works—and what doesn’t—improves safety and effectiveness in using compounds like this. Mature labs should welcome site visits, exchanges, and feedback looping back into product improvement.
A recurring challenge in research is the search for more efficient, less hazardous alternatives. I’ve seen waves of innovation attempt to replace traditional methods using 4-nitrophenylhydrazine, aiming for greener, even more robust chemistry. Some efforts show promise through enzyme-assisted identification, or through digital color recognition tied to automated readout systems. Still, the clarity and reproducibility of hydrazone formation keep the old method in play.
Developments in detection technology—such as smartphone-assisted colorimetry—could breathe new life into established reagents. By automating subtle differences in hydrazone hue or intensity, labs could achieve high-throughput screening with minimal manual oversight. I’ve known teams integrating these approaches, speeding up analysis in settings as varied as food safety checks and biochemistry research.
On a wider scale, new purification techniques such as membrane separation or solid-phase extraction could further enhance efficiency and safety. These advances depend on foundational chemistry—where a reagent like 4-nitrophenylhydrazine keeps its value by staying compatible, reliable, and straightforward to handle.
No compound is perfect. Cost, storage challenges, disposal, and handling risks create friction for many labs, especially where resources run lean. Opportunities exist for chemical suppliers and institutions to make access both safer and more affordable. Bulk purchasing consortia, transparent batch testing, and shared storage infrastructure can all help smooth out these logistical bumps.
On the safety front, I advocate the regular sharing of incident reports, not for blame but for collective learning. Labs sometimes hide close calls out of embarrassment, but open conversations about spills, accidental contact, and safe clean-up protocols would benefit everyone. Resources for in-person and virtual safety training, led by chemists with hands-on experience, could cut down on avoidable mistakes.
From an environmental standpoint, improvements hinge on updated protocols for waste minimization and recovery. Institutions need to re-invest in closed-cycle recycling for hydrazine derivatives, rather than relying on incineration or landfill. I’ve seen pilot programs re-purposing spent hydrazones as starting materials for new syntheses; while not a universal fix, these efforts at least point in a more sustainable direction.
4-Nitrophenylhydrazine, like many chemical reagents, faces tighter oversight as awareness of workplace and environmental safety grows. Countries differ widely in regulatory stringency, but global best practice drifts toward traceability, responsible sourcing, and restricted access for high-risk users. Having spent time both in well-funded and under-resourced labs, I know how frustrating some regulatory hurdles can be—delaying research or raising costs. Supporting legitimate access without sacrificing safety will require better communication between suppliers, regulators, and the research community.
Ethical sourcing can't be an afterthought. Chemists must ask how raw materials and end products move through supply chains, and whether workers producing or handling these compounds have safe conditions. As a scientific community, we owe it to ourselves and society to lead, not follow, in demanding higher standards. Most positive change starts small—a push from inside a single lab, or a demand for batch traceability from a supplier.
Reflecting on decades of laboratory evolution, the role of trusted reagents stays constant amidst waves of change. Reactions that once required luck and guesswork now stand on firmer ground, thanks in part to compounds like 4-nitrophenylhydrazine. The invention of new tools doesn’t erase the value of those we’ve mastered; rather, it highlights the benefits of attention to detail, careful measurement, and ethical practice.
Future directions might see this compound become a model case for responsible reagent lifecycle management, or as a test subject for digital optimization in analytical workflows. Whether trends swing toward automation, green chemistry, or open access, the daily reality won’t shift overnight. Experienced voices in the field continue to shape how both established and emerging chemists interact with these building-block reagents.
In the rush for novelty, foundational work can get overlooked. Yet in countless labs, the small, crystalline pile of 4-nitrophenylhydrazine keeps supporting accurate analysis, smooth synthesis, and confident discovery. The true mark of a valuable reagent rests on three pillars: reliability, safety, and a balance between performance and practical handling. Decades of hands-on experience bear this out—no fancy marketing, just clear, time-tested chemistry.
Those considering their next project or educating the next wave of researchers would do well to reflect on the tools that have made breakthroughs possible. As challenges grow, so does the need for substances that pull their weight without dominating budgets or safety briefings. 4-Nitrophenylhydrazine remains one such ally, proving that the core practices of good science—attention, consistency, and care—still matter most in a laboratory world that grows more complex with every generation.