|
HS Code |
152877 |
| Chemical Name | m-Nitrophenol |
| Cas Number | 554-84-7 |
| Molecular Formula | C6H5NO3 |
| Molecular Weight | 139.11 g/mol |
| Appearance | Yellow crystals |
| Melting Point | 97-99°C |
| Boiling Point | 279°C |
| Solubility In Water | Moderately soluble |
| Density | 1.48 g/cm³ |
| Pka | 8.4 |
| Synonyms | 3-Nitrophenol, m-Hydroxy-nitrobenzene |
| Pubchem Cid | 996 |
As an accredited M-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g amber glass bottle with safety cap, labeled "M-Nitrophenol," hazard pictograms, CAS number, and handling instructions, manufacturer details printed. |
| Shipping | M-Nitrophenol should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is classified as a hazardous material and requires proper labeling and documentation according to regulations. Use secondary containment, and ensure transport is in compliance with local, national, and international chemical shipping guidelines. |
| Storage | **M-Nitrophenol** should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from incompatible materials such as strong oxidizing agents and bases. Keep containers protected from physical damage, moisture, and direct sunlight. Store separately from food and feedstuffs. Properly label all storage containers and ensure access is restricted to trained personnel, following appropriate chemical safety regulations. |
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Purity 99%: M-Nitrophenol Purity 99% is used in high-purity dye intermediate synthesis, where it ensures consistent color yield and product reliability. Melting Point 97°C: M-Nitrophenol Melting Point 97°C is used in pharmaceutical raw material production, where predictable melting behavior facilitates controlled processing conditions. Molecular Weight 139.11 g/mol: M-Nitrophenol Molecular Weight 139.11 g/mol is utilized in laboratory analytical standards, where it provides precise stoichiometry for calibration solutions. Particle Size <10 μm: M-Nitrophenol Particle Size <10 μm is used in pigment formulations, where fine dispersion improves color intensity and uniformity. Stability Temperature up to 120°C: M-Nitrophenol Stability Temperature up to 120°C is used in polymer additive manufacturing, where enhanced thermal stability prevents premature decomposition. Assay ≥98%: M-Nitrophenol Assay ≥98% is used in agrochemical synthesis, where high assay content ensures targeted biological activity. Water Content ≤0.5%: M-Nitrophenol Water Content ≤0.5% is used in battery electrolyte research, where low moisture minimizes side reactions and extends battery life. Refractive Index 1.626: M-Nitrophenol Refractive Index 1.626 is utilized in optical sensor calibration, where accurate refractive properties ensure reliable device performance. pKa 8.36: M-Nitrophenol pKa 8.36 is used in acid-base indicator production, where controlled dissociation improves titration accuracy. UV Absorption Maximum 317 nm: M-Nitrophenol UV Absorption Maximum 317 nm is used in spectrophotometric analysis, where defined absorption enables quantitative detection of analytes. |
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Few chemicals carry as much weight across research, manufacturing, and quality control as M-Nitrophenol. Over the years, I’ve watched labs favor this compound thanks to its reliability and the clear advantages it brings to both academic and industrial workspaces. M-Nitrophenol, or meta-nitrophenol, stands out mostly due to its strong presence as an analytical reagent and starting material while helping researchers prioritize safety, consistency, and purity in their workflows. In the past decade, the breadth of applications for M-Nitrophenol has only grown, with colleagues in pharmaceuticals, agrochemicals, and environmental testing regularly seeking out trustworthy sources and models suited to their goals.
Within the market, “analytical-grade” regularly shows up as the standard for M-Nitrophenol. This label had real meaning in my experience back when I worked in an organic chemistry lab where purity shaped every result. Analytical-grade M-Nitrophenol offers minimal impurities, which is vital during spectrophotometric analyses or in processes that demand unflinching consistency. Purity levels typically reach at least 99%, verified by spectral and chromatographic methods. The familiar yellow crystalline solid presents itself with a melting point between 96 and 98°C, acting as a reliable indicator of quality and purity.
Customers in research and industry quickly learn that powders from reputable vendors avoid contamination, showing uniform granulation, free flow, and easy dissolution in solvents like ethanol and warm water. These properties come up over and over in conversations with lab techs, who tell me a reliable batch of M-Nitrophenol translates into fewer headaches and smoother reference-value calibrations. A misstep, like trace moisture content above 0.5%, can upend entire analysis runs or chemical syntheses—so reputable suppliers always offer supporting data verifying batch-to-batch uniformity through maintained certificate records or third-party quality checks.
M-Nitrophenol probably pops up most often in the creation and testing of dyes, pesticides, and pharmaceuticals. I remember seeing it on countless shelf labels in analytical labs, often serving as a robust colorimetric standard. M-Nitrophenol’s reliable absorbance in UV/Vis spectrophotometers remains crucial for enzyme kinetics research, where laboratory workers require reference substances that won’t skew data at targeted wavelengths, usually around 410 nm. More than once, I saw how a shift in product grade—even a small purity deviation—threw off calibration curves, underscoring why so many labs trust only high-quality supplies after seeing what happens when standards slip.
Chemical synthesis teams lean on M-Nitrophenol while building complex molecules, especially as a building block for intermediates in active pharmaceutical ingredients or crop protection compounds. Strong nucleophilicity and predictable reaction behavior set M-Nitrophenol apart among available nitrophenols—it consistently enables clean downstream reactions, minimizing the need for repeated purification runs. For production chemists, reducing remediation and rework means more time for innovation, less expenditure on raw materials, and a smaller environmental footprint.
Beyond industrial-scale synthesis, environmental labs take advantage of its well-characterized breakdown patterns. Analytical teams can monitor water samples for nitrophenol residues, using M-Nitrophenol as a benchmark. Clear separation during HPLC or GC assays makes it a standard reference for method validation, which remains essential when regulatory auditors review wastewater discharge data or drinking water profiles. Those details make a difference for environmental chemists, who count on standards being not just pure, but traceable and accurate.
I’ve never met a chemist who doesn’t respect M-Nitrophenol for its dual character: useful, but also potent enough to demand care. Its mild toxicity means lab managers treat storage and disposal with gravity. It always made sense—once spilled or mishandled, even a small mass can pose risks to health and the environment. Gloves, goggles, and fume hoods become standard not because of needless caution but from long years of lessons learned through accidents and overexposure episodes. Responsible companies design labeling and packaging for clarity and longevity, using robust seals and tamper-resistant features that signal any compromise to integrity.
Part of the modern supplier’s job involves guiding institutional clients through green chemistry and waste minimization as well. I’ve watched labs cut waste by ordering sealed ampoules with pre-measured doses, slashing unnecessary excess and minimizing the burden of chemical storage and residual disposal. Investing in less waste yields cost savings and aligns with evolving environmental regulations that grow stricter each year. Companies bringing M-Nitrophenol to market these days back those sustainability claims with lifecycle data—the better vendors offer documentation showing compliance with international norms for safe transit, labelling, and ecological management of byproducts.
Anyone who’s handled both M-Nitrophenol and its ortho- or para-isomers picks up on some key distinctions. These positional isomers (o-nitrophenol and p-nitrophenol) differ mainly in where the nitro group sits on the benzene ring. That small change brings out measurable shifts in melting point, solubility, toxicity, and reactivity. From a hands-on perspective, o-nitrophenol dissolves better in nonpolar solvents and shows distinct spectral properties, while p-nitrophenol often plays a bigger role in pharmaceutical syntheses due to its higher reactivity in some substitution reactions.
M-Nitrophenol really claims its niche in enzyme kinetics and dye chemistry, standing out for reliable absorption maxima and chemical stability in different pH conditions. I recall running parallel assays with all three major nitrophenol isomers; meta consistently delivered steadier baseline readings and fewer outliers thanks to that signature stability. This behavior makes it the go-to choice for settings where accuracy overrides any need for unique reactivity features. It doesn’t completely outclass the others—there are tasks better suited to ortho or para isomers—but its stable reaction profile and manageable handling characteristics keep M-Nitrophenol high on procurement lists worldwide.
In quality control, labs value the meta version because its impurities and byproducts stand out under standard detection conditions—less ambiguity means fewer false positives, which matters during regulatory submissions. Some labs turn to M-Nitrophenol as a calibration reference just for the confidence it brings. The peace of mind comes not from abstract ideas, but from knowing years of peer-reviewed studies and industry practice demonstrate what to expect from a batch that meets accepted grades.
As green chemistry and sustainability take center stage, the chemical industry faces growing pressure to supply materials that minimize waste and human risk. Producers now look for sustainable manufacturing routes for M-Nitrophenol, including cleaner catalytic nitration processes and improved recovery of raw phenol feedstocks. My conversations with plant managers show a growing interest in traceability and closed-loop lifecycle management, driving up demand for products supplied with comprehensive documentation, transparent sourcing, and measurable reduction in hazardous byproducts.
Customers have also become more detail-oriented about packaging and documentation, pressing vendors to supply analytical reference standards alongside every shipment. Labs expect supporting HPLC, NMR, or mass spectroscopy data attached to certificates of analysis. Even academic groups push for this traceability, led by graduate students frustrated with inconsistent stock standards holding back their experiments. The era of anonymous bulk chemicals has faded—in its place stands a heightened expectation for transparency and end-user safety from purchase to disposal.
Research groups buying M-Nitrophenol start to scrutinize not just what they’re getting, but also who produced it and how. A trusted reputation carries as much weight as the technical data. Researchers don’t just want a perfect melting point; they want to know the supplier backs up every batch with a proven chain of custody and meets ISO or GMP standards. Peer-reviewed literature remains filled with references to M-Nitrophenol’s spectral signatures, reactivity, and handling precautions, giving purchasing managers and safety officers guidelines on how best to integrate it into ongoing projects.
Technical teams sometimes face a quandary balancing cost and reliability. In my experience, the lower-cost, industrial-grade batches may save money up front, but the risk of trace contaminants can quickly eat away those savings when you’re troubleshooting spectral oddities or unexpected byproducts downstream. For high-sensitivity analyses and production of regulated end products, the upfront cost of analytical-grade M-Nitrophenol usually pays off through time saved, results gained, and headaches avoided. Strong documentation and supplier accountability give buyers another layer of protection, letting them prove compliance if auditors ask for a paper trail.
Even among specialists, errors in handling or misidentifying nitrophenol isomers can create trouble. I once consulted on a case in a university lab where mislabeled samples led to weeks of wasted effort tracing the source of unexpected reagent behavior in enzyme assays. Situations like this underline the need for proper labelling, clear supplier certification, and improved site-level chemical inventory systems. Adopting robust digital tracking platforms—tied directly to supplier-provided QR codes—has become more common, offering real-time status of inventory, lot numbers, and expiration dates.
Beyond identification issues, storage conditions play a huge role. M-Nitrophenol, like most nitroaromatics, remains stable under dry, cool, and well-sealed conditions, but falls prey to slow degradation from light and humidity. It’s not uncommon for academic labs, pressed for space, to stash chemicals wherever they fit, only to wind up with clumped, discolored material a few months later. Training staff and students about best storage practices—along with investing in good secondary containment and warning signage—cuts down on accidental exposure and product loss. An upfront outlay for better storage pays dividends in both efficiency and peace of mind, especially in shared facilities with frequent personnel changes.
Disposal remains an area of ongoing conversation. Outdated methods simply relied on down-the-drain practices or landfill disposal, but the risks of environmental persistence and waterway contamination have prompted universities and companies to work with specialized waste contractors. Newer protocols encourage chemical neutralization and centralized hazardous waste management, which not only complies with regulatory mandates but also protects community health. Some suppliers have started offering takeback programs for spent or outdated chemicals, which helps smaller labs avoid the headache of negotiating with third-party disposal companies by themselves.
Transferring good practice surrounding M-Nitrophenol relies on solid training and communication. Fresh graduates or industry hires don’t always receive enough hands-on instruction, and mistakes or unsafe shortcuts can slip in. I’ve watched safety officers at major pharmaceutical makers formalize onboarding lessons for new chemists who handle hazardous organics, using real-life case studies to drive home the practical consequences of mishandling. More universities now incorporate hands-on safety modules in advanced organic labs, walking students through proper weighing, dilution, and cleaning so the lessons stick past graduation.
Community forums—ranging from research association listservs to international chemistry groups—structure ongoing discussion around best practices for M-Nitrophenol usage. Researchers openly share chromatographic data, unusual reaction outcomes, or clever solutions for integrating greener practices. This spirit of openness lets workers in isolated labs, or in small companies, keep up with the broader field. Vendor partnerships work best when backed with technical support hotlines and quick-turnaround analytical consulting; this close link between buyer and seller doesn’t just result in better outcomes, but also lowers the risk of user error or material waste.
Data accuracy stays at the heart of M-Nitrophenol’s value. Analytical chemists don’t just hunt for low cost—they need to trust that the figures attached to each bottle reflect reality. In regulatory environments, like those overseeing pharmaceutical ingredients or water quality, this confidence becomes non-negotiable. Peer-reviewed studies and supplier reports keep information flowing and let buyers benchmark one supplier against another. Timely sharing of analytical data—such as recent findings on thermal stability or compatibility with evolving chromatographic methods—means new users can leapfrog past avoidable pitfalls encountered by others in comparable workflows.
Better transparency isn’t just a buzzword—it makes a measurable difference at the lab bench, in procurement offices, and on the shop floor. As competition for high-quality M-Nitrophenol heats up, buyers and users shape demand for tighter quality controls, more detailed characterization, and environmentally responsible management throughout a product’s lifecycle. Procurement teams increasingly request detailed supporting data, and vendors who respond build lasting relationships instead of quick sales. Some research consortia have proposed supplier accreditation programs that score vendors not just for chemical quality, but also documentation robustness, support offerings, and environmental responsibility—a step toward boosting confidence and weeding out inconsistent sources. I’ve seen entire departments shift purchasing decisions based on a vendor’s willingness to provide in-depth product support and lifecycle disposal guidance.
Digitization has started to close the loop across the product chain. Integrated lab management software now tracks every batch from receiving dock to final disposal, with traceability systems catching everything from accidental isomer switches to improper storage events. Sharing storage and usage data with suppliers lets companies and institutions catch trends over time—like upticks in waste volume or repeated calibration errors—leading to proactive training or adjustments in stock levels. Over time, labs documenting best practice and sharing anonymized process data with the scientific public lift standards and help keep everyone safer.
Industry groups and regulators pay attention to incidents of accidental exposure or contamination, sometimes using those events to strengthen guidance and safety checklists. Experienced workers take pains to record both what went right and what went wrong each year, building up a cultural memory that newcomers can draw on. Progress toward greener, safer M-Nitrophenol isn’t just technical—it’s about keeping knowledge mobile and practical. Training modules, vendor white papers, and internal newsletters all play a role.
My time alongside procurement, synthesis, and quality assurance teams hammered home the value of choosing suppliers and product models with a reputation for precision, dependability, and open customer service. M-Nitrophenol’s journey from manufacturing plant to laboratory bench involves many steps, any of which can affect the final product’s usefulness and safety. Consistently achieving a 99% purity level, documented by certification and batch testing, speaks to robust manufacturing control—one that experienced researchers explicitly seek out for high-stakes projects or regulated end uses.
Sourcing from companies committed to safety and compliance protects not only the work but also communities and the environment. Labs have started to shift toward suppliers that preemptively provide safe use guidelines, waste handling advice, and compliance verification with regulatory frameworks. Requirements for product traceability and guarantee of batch integrity have quickly evolved from nice-to-have features to basic prerequisites. As the burden of responsibility falls on every link in the supply chain, a culture of accountability arms workers and companies with the best odds of consistent, reproducible, and safe work.
Working with M-Nitrophenol demands more than technical skill—it asks for attention to the details of documentation, communication, and continuous improvement. Every user, from undergraduate students dipping a test strip for the first time to seasoned industrial chemists running three-shift production lines, has a stake in a shared standard of care. Peer-reviewed references, real-world case studies, and robust technical support let everyone make informed decisions, minimizing both risk and wasted opportunity across the board.
As regulations evolve and customer expectations push higher, the chemical industry sees M-Nitrophenol not just as another substance, but as a focal point for meaningful collaboration. Suppliers who listen to customers’ needs and provide thorough, transparent information—backed with accurate documentation—lay the groundwork for safer, more efficient, and more sustainable operations. Shared effort leads to better results for both science and society.