|
HS Code |
462693 |
| Chemical Name | O-Nitrophenol |
| Synonyms | 2-Nitrophenol |
| Molecular Formula | C6H5NO3 |
| Molecular Weight | 139.11 g/mol |
| Cas Number | 88-75-5 |
| Appearance | Yellow crystalline solid |
| Melting Point | 44-46 °C |
| Boiling Point | 216 °C |
| Solubility In Water | Moderately soluble |
| Density | 1.48 g/cm³ |
| Flash Point | 170 °C |
| Pubchem Cid | 975 |
| Odor | Phenolic odor |
As an accredited O-Nitrophenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | O-Nitrophenol is supplied in a 500g amber glass bottle with a screw cap, labeled with hazard symbols and product details. |
| Shipping | O-Nitrophenol should be shipped in tightly sealed containers, protected from light and moisture. It must be kept away from heat, sparks, and incompatible substances such as strong oxidizers. Label containers with proper hazardous warnings and handle in accordance with local and international regulations. Transport in compliance with DOT, IATA, and IMDG guidelines. |
| Storage | O-Nitrophenol should be stored in a tightly closed container, in a cool, dry, well-ventilated area away from heat, sparks, open flames, and incompatible substances such as strong oxidizers and strong bases. Protect it from light and moisture. Handle with care, using appropriate protective equipment, and avoid prolonged or repeated exposure to air. Store at recommended temperatures and label clearly. |
|
Purity 99%: O-Nitrophenol purity 99% is used in pharmaceutical intermediate synthesis, where high-purity ensures minimal byproduct formation. Melting Point 45°C: O-Nitrophenol melting point 45°C is applied in azo dye manufacturing, where precise phase transition enables consistent dye quality. Molecular Weight 139.11 g/mol: O-Nitrophenol molecular weight 139.11 g/mol is utilized in analytical reference standards, where accurate mass provides reliable calibration. Particle Size <20 µm: O-Nitrophenol particle size <20 µm is used in catalyst preparation, where fine dispersion improves catalytic activity. UV Absorbance 430 nm: O-Nitrophenol UV absorbance 430 nm is employed in spectrophotometric enzyme assays, where defined absorbance supports sensitive enzymatic activity measurement. Stability Temperature up to 80°C: O-Nitrophenol stability temperature up to 80°C is used in biochemical research protocols, where thermal stability prevents compound degradation. Water Solubility 20 g/L: O-Nitrophenol water solubility 20 g/L is incorporated in environmental pollutant modeling, where solubility data ensures accurate simulation results. Assay ≥98%: O-Nitrophenol assay ≥98% is used in laboratory synthesis of fine chemicals, where high assay ensures reproducible yield. |
Competitive O-Nitrophenol prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
O-Nitrophenol, often recognized for its pale-yellow crystal form, has carved out a distinctive place in the world of manufacturing and laboratory research. Its model—commonly referred to based on its chemical structure as 2-nitrophenol—offers solid value for several industries, largely because of its chemical reactivity and purity standards. Reliable O-Nitrophenol comes in solid, crystalline form and typically ranges in purity from 98% up to a standard of 99%. This ingredient often finds purpose in creating dyes, pharmaceuticals, and as an intermediate in pesticide production. It separates itself from similar compounds like P-Nitrophenol through both chemical properties and practical usage.
Looking at this compound under a microscope, you see a benzene ring featuring both a hydroxyl and a nitro group in ortho positions. This simple arrangement gives O-Nitrophenol its unique chemical nature. Because the hydroxyl and nitro groups sit next to each other, O-Nitrophenol shows higher acidity compared to other isomers such as P-Nitrophenol. This modest shift in structure makes a significant difference in how the compound behaves in lab reactions. As a result, when precise pH response or targeted reaction pathways matter, O-Nitrophenol becomes a preferred choice.
I’ve spent years in research labs, running routine spectroscopic analyses with O-Nitrophenol. For chemists, nothing gets more frustrating than working with inconsistent chemicals. When you know the exact model and can count on a predictable melting point—between 44 and 46°C for O-Nitrophenol—you get fewer surprises, less noise in your data, and better reliability from experiment to experiment. This lets us trace reactions in real-time and makes for cleaner results.
Years ago, while optimizing enzyme assays, I found O-Nitrophenol indispensable. The compound, under alkaline conditions, gives a bright yellow solution whose intensity tells you exactly how much reaction happens over time. That clarity changes the game—there’s no fumbling around with ambiguous color changes or inconsistent reactions, unlike what I faced using other phenolic compounds. Each test ran faster, saving not just labor but also costs in materials and wasted time.
In dye manufacture, O-Nitrophenol acts as a solid building block. It transforms into azo dyes that color textiles, plastics, and even cosmetics. Textile engineers care about this quality—when using high-grade O-Nitrophenol, shades come out consistent across materials and batches. One significant benefit comes from its solubility in hot water and common organic solvents, which lets manufacturers blend it smoothly into large-scale production without headaches.
Pharmaceutical researchers count on the predictable reactivity of O-Nitrophenol. This lets them derive useful medications or run clean reactions when building more complex molecules. The nitro group, for instance, provides a gateway for reduction reactions, leading to medication ingredients and agricultural chemicals. When trace impurities interrupt these sensitive syntheses, costs climb and progress slows—choosing quality O-Nitrophenol sidesteps these direct, real-world frustrations.
Chemists regularly compare O-Nitrophenol with its cousins—m-nitrophenol and p-nitrophenol. O-Nitrophenol, with its adjacent functional groups, serves more specialized purposes. In organic reactions, its ortho configuration means it participates in hydrogen bonding, leading to a lower melting point and different solubility behaviors. I recall scenarios in lab settings where choosing between p-nitrophenol and o-nitrophenol wasn’t about availability—it was about what the experiment demanded. Trying to swap the two produced weaker results, especially during routine quality tests on run-down equipment, or in reactions where pH sensitivity played a major part.
These little differences matter. P-nitrophenol usually works best as an enzyme substrate because of its vibrant yellow color and higher melting point, but it can’t always substitute neatly for O-Nitrophenol in more challenging syntheses. Each nitrophenol isomer takes its particular niche; those details, while easy to overlook, mean that industrial buyers and chemists alike come back to O-Nitrophenol for projects where outcomes depend on precise chemistry rather than catch-all substitutes.
Reliable sourcing for O-Nitrophenol remains key for buyers and researchers who want consistent results. Sub-standard grades, often a result of poor purification or mishandled supply chains, stop progress in its tracks. Think of a batch of O-Nitrophenol that contains barely noticeable contaminants—which still have the power to slow or inhibit crucial reactions. I’ve personally watched entire research runs voided by unexpected reactivity or sorption to container walls. Those headaches translate into costs far greater than the savings from chasing bargain-rate chemicals.
Quality producers test every lot through melting-point checks, chromatographic purity, and moisture measurement. Analytical labs need chemicals with known backgrounds; otherwise, data starts looking fuzzy, difficult to reproduce, or outright misleading. These pain points push responsible users and manufacturers away from shady importers and toward suppliers who show open documentation and clear tracking.
O-Nitrophenol isn’t just a laboratory curiosity. It finds its way, through runoff or discharge, into the wider environment. Teachers drilling safety routines into young scientists will always stress the importance of good lab habits. After handling this compound, proper neutralization and storage keep both people and environments safer. Breathing in O-Nitrophenol dust or vapors can irritate mucous membranes. Direct skin contact leads to irritation as well, something lab veterans learn quickly. Workplace safety rules expect use of gloves, goggles, and ventilated enclosures for just these reasons.
Municipal treatment systems and regulatory frameworks now include stricter guidelines for handling and disposal of nitrophenols. Factories and academic labs benefit when they spend time upfront on proper containment and waste treatment rather than scrambling for damage control after spare-lit accidents or improper disposal. I’ve witnessed the contrast between organizations who treat these rules as afterthoughts and those who engrained them into daily routine—issues always catch up with the unprepared. Responsible use, thorough records, and state-of-the-art neutralization processes save trouble in the long run.
Supply chain reliability sits among the biggest worries for regular buyers of O-Nitrophenol. Production stoppages, shipment delays, or fluctuating purity levels directly affect downstream operations. For example, a pharmaceutical company racing to develop new treatments can’t afford to suspend synthesis half-way because a shipment of O-Nitrophenol hit customs delays or failed purity checks. Businesses now seek closer partnerships with suppliers, looking beyond price tags and toward transparency throughout procurement and production.
Even with best efforts, not every setback finds a quick fix. Economic uncertainty, regulatory changes, or sudden raw material shortages can restrict available supplies. Managers and chemists who keep close tabs on trending quality reports and make contingency plans end up better equipped to weather storms. Buffer inventories, direct dialogue with suppliers, and investment in more flexible in-house purification techniques build in resilience for hard times.
Technology keeps raising expectations in chemical manufacturing. Demand grows for cleaner, greener, and more sustainable production routes—not just for O-Nitrophenol but for every ingredient in the chemical toolbox. With tighter environmental oversight and consumer awareness, producers rethink traditional methods that produced unwanted byproducts or hazardous waste. Cleaner conversion processes, renewably sourced inputs, and responsible waste management have become vital focus areas.
Researchers now look at catalytic routes and solvent-free alternatives for making O-Nitrophenol. Each incremental improvement means less pollution, lower costs, and fewer headaches for workers and local communities. While no transition comes easy, the pressure pushes producers toward balance—delivering the reliability and reactivity people expect from O-Nitrophenol while minimizing the environmental footprint.
Companies and universities can take a fresh look at their O-Nitrophenol handling and use. Establishing robust protocols from sourcing through waste disposal forms the bedrock of better practice. Setting up regular quality audits lets teams spot potential trouble early, while feedback loops with trusted suppliers work to resolve small issues before they snowball. I’ve seen projects where frequent communication led to early delivery of high-grade material and helped salvage critical deadlines.
On-site storage practices also come under review. Keeping O-Nitrophenol in airtight containers, in cool and dry spaces, helps guard against moisture uptake and degradation. Clear labeling and segregated storage, especially in settings with other potentially reactive organics, matter more than many realize until a mishap occurs. Each decision in the storage chain—right down to keeping containers sealed and clearly marked—prevents waste, spoiling, and hazards down the line.
In the world of research and education, keeping thorough documentation of each batch used injects much-needed clarity into experimental records. When results don’t align, you can trace back to changes in raw material lots or shifts in supplier performance. Comprehensive records let teams learn from past mistakes, drive improvement, and deliver on ambitious research goals.
Countries worldwide now pay closer attention to chemicals like O-Nitrophenol through updated safety and environmental controls. New rules often set stricter upper limits for trace levels in discharge water and waste. That shift forces manufacturers to innovate, whether by deploying new scrubbing technologies, capturing emissions at the source, or recirculating waste streams. I’ve spoken with managers who once resisted change and later praised the benefits gained through cleaner compliance—fewer inspection headaches, smoother audits, and stronger community goodwill.
In research and educational settings as well, compliance isn’t just about ticking boxes. It’s become a springboard for better science—forcing teams to adopt more exacting tracking, safer handling, and creative ways to minimize leftover waste. In my own lab days, paperwork and audit trails sometimes felt tedious, but they brought a sense of confidence and safety among new trainees and seasoned staff alike. Regulators don’t slow progress; they bring structure and shared responsibility that benefits both industry and society.
O-Nitrophenol’s appeal hinges on a set of tangible, real-world qualities. Its crystallized form, reliable melting point, and rich chemical reactivity set it apart from look-alike ingredients. Whether working on a new azo dye, conducting a colorimetric enzyme assay, or preparing foundational materials for agrochemicals, it provides consistent, predictable performance. Small differences in structure create enormous changes in utility—reminding us that details in chemistry carry weight in the real world.
My enduring experience with O-Nitrophenol echoes what others in manufacturing, research, and education keep discovering: choosing the right tool for the job always pays off. Rushed switches to substitutes lead to longer troubleshooting and greater cost over time. By sticking with high-quality, well-documented O-Nitrophenol, projects stay on track and performance stays at its peak.
As chemistry pushes toward greener processes, attention shifts toward both performance and responsibility. Forward-thinking teams invest effort into understanding the lifecycle of every chemical. They treat waste at the source, minimize escape routes, and select reagents that leave smaller marks on the environment. For O-Nitrophenol, that journey features breakthroughs in production, safer handling, and stronger accountability to health and safety norms.
Taking the long view, balancing industry’s need for effective reagents with society’s demand for cleaner operations brings challenges and fresh opportunity. O-Nitrophenol continues to stand out not just for what it enables on the factory floor or in a research flask, but for the ways its supply chain, use, and stewardship evolve as the world demands more from its chemicals and its chemists.