|
HS Code |
381609 |
| Chemical Name | 2-Acetamido Phenol |
| Cas Number | 614-80-2 |
| Molecular Formula | C8H9NO2 |
| Molecular Weight | 151.16 g/mol |
| Appearance | White to off-white crystalline powder |
| Melting Point | 164-168°C |
| Boiling Point | Unknown or decomposes |
| Solubility In Water | Slightly soluble |
| Density | 1.32 g/cm³ |
| Synonyms | N-(2-Hydroxyphenyl)acetamide, o-Acetaminophenol |
| Pubchem Cid | 11811 |
| Smiles | CC(=O)NC1=CC=CC=C1O |
As an accredited 2-Acetamido Phenol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 2-Acetamido Phenol, sealed with a screw cap, labeled with safety and handling instructions. |
| Shipping | 2-Acetamido Phenol is shipped in tightly sealed containers, protected from moisture and light. It should be handled in compliance with chemical safety regulations, including labeling and documentation. Transport is typically via ground or air freight as a non-hazardous material, ensuring the package remains upright and secure to prevent spillage or contamination. |
| Storage | 2-Acetamido Phenol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect it from light and moisture. Properly label containers and prevent physical damage. Ensure compliance with relevant safety protocols and local regulations for chemical storage. |
Competitive 2-Acetamido Phenol prices that fit your budget—flexible terms and customized quotes for every order.
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Tel: +8615380400285
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In the world of chemical manufacturing, 2-Acetamido Phenol stands out as a versatile intermediate that sees daily demand across several industries. Those who spend time in a plant or QC lab know the importance of dependability in supply, and this product consistently proves essential in pharmaceutical synthesis, agrochemical development, and specialty chemicals manufacturing. Drawing on experience handling bulk orders as well as custom volumes, we understand the expectations placed on every shipment, not just for purity but for consistency and clear traceability—from raw material intake to the final drum or bag leaving our facility.
We produce 2-Acetamido Phenol through controlled processes, using high-grade feedstocks and running exhaustive spot checks to make sure each lot meets strict HPLC analysis and melting point specifications. For current batch production, our material usually measures a melting point between 163°C and 165°C, remaining free of visible contamination. Refinement doesn’t stop at chemistry; our teams monitor moisture content and residual solvents, knowing how even minor deviations can affect downstream reactions or cause unforeseen issues for partners in synthesis or formulation.
From a practical standpoint, years spent troubleshooting order requirements with technical staff at pharma and dye houses taught us the difference between paper specs and chemical realities. Purer product saves solvent, reduces purification steps, elevates yield, and lowers batch failure rates. We address hidden costs—losses from off-spec lots, filter blockages, spent hours in reprocessing—and design our manufacturing with these real shop-floor frustrations in mind.
Our 2-Acetamido Phenol, commonly known by its chemical synonym Acetaminophenol or N-(2-hydroxyphenyl)acetamide, sees regular use in the synthesis of pharmaceuticals and intermediates that demand high reactivity from both the acetamido and phenolic functional groups. Customers regularly need it for step-growth in active pharmaceutical ingredient pipelines, dye development, and agricultural research compounds.
Many end-users leverage our material to build acetaminophen derivatives, azo dye couplers, or selective herbicide agents where consistent structural purity makes or breaks batch acceptability. Reliability in phase transfer catalysts and select polymer chemistry applications comes from highly uniform particle distribution. Decades of collaboration with end users taught us that clean spectra and repeatable responses to common analytical tests (often FTIR, NMR, and mass spec) help avoid downstream surprises, especially in regulated environments.
Not every 2-Acetamido Phenol on the market performs the same way. Production methods lead to wide variations in color, sizing, and solubility. Finer powders open up new options for blending in advanced pharmaceutical tables and facilitate more even suspensions in manufacturing high-performance coatings. Larger, free-flowing crystals appeal to users seeking minimal fines and easier filtration. After repeated feedback from formulators frustrated by clumping or inconsistent dissolution rates, we modified our drying and milling stages for improved pourability and wettability.
We see first-hand how minor impurities, even below textbook detection thresholds, can poison catalysts, lead to stalled reactions, or produce off-shaded batches in dye production. Beyond what shows up on a certificate of analysis, our labs spot-check by GC-MS and watch for hard-to-detect organics that can compromise costly multi-step syntheses. The result is that users report cleaner extraction phases and improved product stability from our lots, minimizing time spent resolving process deviations traced back to raw materials.
Rather than flooding material out as commodity product, we structure lot releases around feedback from plant chemists and QC professionals. Current production models deliver assay values exceeding 99 percent by HPLC, typical moisture content below 0.2 percent, and minimal residual organic solvents. Almost every day, our technical team gets asked about how slight shifts in assay or particle size can throw off downstream performance; we track and adjust batches to minimize those headaches.
Years spent troubleshooting the unexpected—fines gumming up tableting equipment, or trace metal contaminants derailing a high-purity synthesis—convinced us to keep tighter in-house standards than even some pharmacopeia references. Specific heavy metals (lead, arsenic, mercury) remain at trace or nondetectable levels, and our cleaning and separation steps cut cross-contaminant risk, a concern for any GMP operation.
Plant operations run at their best only with robust, documented procedures. Our batch production lines use process controls for temperature, solvent ratios, pH balance, and time, with live tracking of key parameters shared internally for every lot. We build in traceability for each input through the entire production chain, cataloging dates, personnel, and test data so that if a client flags an issue, a concrete root-cause investigation can dive straight to the source.
Frequent requests for technical documentation drove us to streamline access to batch timelines, material safety data, and purity analytics for each shipment. Customers with validated processes and regulatory compliance concerns receive digital copies on delivery, making both internal audits and third-party inspections move faster—less downtime, less lost product.
Much can go wrong between production and end use; weight shifts, humidity ingress, abrasion during transport, all these can destroy months of careful preparation. To minimize damage and loss, we select packaging according to order volume and transport conditions. Typical shipments leave in sealed fiber drums, double-layer lined bags, or smaller HDPE containers for laboratory quantities. After repeated rounds of transit-testing, we adjusted sealants and liners to cut the risk of airborne moisture or fragmentation under vibration.
Custom requests often arrive for inert gas-blanketed packaging, and our operations team works directly with logistics partners to verify pallet handling and stacking procedures. This routine contact helps minimize risk of compromised lots or unexpected quality holds, especially for international shipments facing unpredictable customs environments.
Beyond the technical focus, we foster a mindset that quality starts with people. Regular employee involvement in safety reviews and improvement brainstorms reveals bottlenecks on the line, waste habits from packaging, and overlooked QC steps. As a manufacturer, we’ve had our share of surprise recalls and frustrating near-misses; that gives us an honest perspective when evaluating how our products affect customers’ downstream equipment uptime and output reliability.
Continued investment in technician training means line workers recognize atypical color shifts, texture changes, or odor anomalies, flagging possible batch problems before they move to storage or shipping. The sum of these efforts appears in the form of fewer out-of-spec deliveries reported from regular customers and plenty of return orders from those who previously struggled with inconsistent sources.
Our decades in chemical manufacturing show that cost cutting only succeeds up to the point it starts creating bigger downstream risks. By sticking with higher-standard purification columns, better controlled-reactor environments, and rigorous cross-cleaning of all batch-handling equipment, we secure higher yields and fewer product-quality complaints. The decision to invest in advanced detection for process contaminants and trace metals came after repeated unsought lessons from customer feedback, QC failures, and, on rare occasions, lost contracts.
Whereas much of the market attempts to push out low-cost, minimally screened lots, risking unpredictable shifts in color or reactivity, our focus remains on delivering the performance and reliability that professional end-users actually need. Customer production launch failures traceable to raw material volatility gave our team a clear priority: only send lots that support predictable, repeatable chemistry in actual plant conditions, not just on paper. This principle keeps both our partners and our operations moving forward.
Nearly every technical issue that makes it to our office—failed HPLC readings, crystalline changes, clogged process filters—brings a story of risk-avoidance improvements. We don’t forget the batch of off-white crystals delivered to a pharma line that triggered a two-day halt, or the case where a minor impurity blocked a dye developer for a major textile brand. Instead of treating these as isolated “user errors,” we re-engineer processes.
Feedback from these experiences led to routine lot-by-lot colorimetric analysis, more frequent Karl Fischer titrations, and improved documentation standards. Each time a facility reports smoother product conversion or ease in regulatory review, our teams share those insights to refine the next run, improving the product and strengthening relationships throughout the value chain.
Compliance matters not just as a checkbox but as a direct safeguard for customers who build complex syntheses or face pharmaceutical inspections. We worked alongside regulatory consultants, R&D chemists, and customer QA teams to align product releases with the latest national and international guidelines. As rules update to call for tighter limits on trace contaminants or explicit allergen declarations, our labs run updated protocols to stay ahead of compliance risks.
Batch records, change logs, and full traceability info routinely accompany shipments. Regulatory audits, both surprise and planned, prompted us to create digital archives for every run, accessible for both internal QA and to support any customer investigation. Understanding the way auditors scrutinize records, we prepare clean and accessible documentation that matches on-the-ground production with stated analysis.
In practice, any end-user depending on 2-Acetamido Phenol as a starting material sees more than just a bag or drum of chemical—they see the cumulative impact on process time, finished quality, safety, and production economics. The reliability of our lots reduces the risk of costly rework, loss of critical production windows, or customer quality complaints down the line. Customers routinely report that early, clear notification of any shift in physical characteristics, specification changes, or process notes matches more closely with actual plant constraints than standardized “certified” generic documents.
The day-to-day work inside our plant and customer feedback cycles keep us grounded in the shared pressures faced by operators, chemists, and procurement specialists. That lived experience creates a feedback loop where product design and process control reflect hands-on challenges—not theoretical, but encountered in real-world usage.
Working as an active manufacturer rather than a trader, we distinguish our product from commodity alternatives or variable importer-sourced lots. Many competitors, focused exclusively on minimum cost, take an approach that risks unpredictable OELs, inconsistent shading, and variable bulk density. End users can encounter issues with unwanted byproducts, higher insoluble matter, or unexplained batch failures after switching to these sources.
Our direct control and traceability, from synthetic steps to final QC, means minimal lot-to-lot variation, which downstream QC teams often recognize immediately. Working in close contact with customers’ technical staff, we respond to industry-driven demands for custom grades, tighter sieve fractions, or packaging solutions tailored for GMP zones. Users working under regulatory scrutiny find our documentation and transparency fill the gaps left by generic products that fail to account for the true needs of regulated or high-purity production.
Production teams dedicated to continuous improvement draw extensively on real production feedback loops. In our facilities, we utilize “lessons learned” logs from actual troubleshooting calls, recalling everything from unexpected moisture absorption to surprise foaming in a customer’s reactor during summer heat. Regular engineering reviews probe root causes and push our teams to refine both testing and process flows.
Focused customer site visits and open lines for technical consultation drive process adaptations—small changes to grinding step parameters, reagent charge timings, or packaging reinforcements to fit varied requirements. Incorporating these grounded, practical findings directly improves product usability and customer outcomes.
As target applications for 2-Acetamido Phenol evolve, our plant teams partner closely with R&D units to anticipate new requirements—whether in higher purity for API synthesis, improved handling for automated feed equipment, or specialty grades for non-pharma sectors. Working at the nexus of real chemistry lab challenges and scaling industrial batch runs, we remain positioned to deliver innovations that address genuine needs.
Feedback from developmental chemists—ranging from updated solubility targets to unique flow characteristics—often leads to pilot-scale trial batches ahead of large-scale changes. This collaborative R&D mindset supports not only new end-market opportunities but also strengthens long-term relationships, eliminating the sense of distance that can crop up between supplier and user.
Every aspect of our operation, from raw material vetting to real-time batch tracking, reminds us of the stakes customers face. We do not view these as abstract opportunities for optimization but as day-in, day-out challenges to be solved with scientific precision, transparency, and a willingness to adjust course when the evidence demands it.
Our daily work as a direct manufacturer, with hands-on visibility over each reaction, separation, and packaging step, brings a level of confidence in the finished product that third-party resellers rarely achieve. In ensuring high, reproducible purity, minimized contaminants, and trustworthy documentation, we help end users avoid costly missteps and support them in producing materials that meet exacting standards for quality and safety.
