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HS Code |
249810 |
| Chemical Name | N-Methylacetanilide |
| Synonyms | N-Methyl-2-acetanilide |
| Molecular Formula | C9H11NO |
| Molecular Weight | 149.19 g/mol |
| Cas Number | 530-75-6 |
| Appearance | White to off-white solid |
| Melting Point | 90-92 °C |
| Boiling Point | 302 °C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.09 g/cm³ |
| Smiles | CC(=O)NC1=CC=CC=C1C |
| Inchi | InChI=1S/C9H11NO/c1-8-6-4-3-5-7-9(8)11-10-2/h3-7H,1-2H3,(H,10,11) |
As an accredited N-Methylacetanilide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250g of N-Methylacetanilide is supplied in a sealed amber glass bottle with a secure screw cap, labeled with hazard information. |
| Shipping | N-Methylacetanilide should be shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It must comply with local, national, and international transportation regulations. The chemical should be clearly labeled, handled by trained personnel, and accompanied by a Safety Data Sheet (SDS) during shipping to ensure safe and compliant transport. |
| Storage | N-Methylacetanilide 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 moisture and direct sunlight. Ensure the storage area is equipped to handle spills safely and is clearly labeled to prevent unauthorized access or accidental misuse. |
Applications of N-Methylacetanilide in Industrial ManufacturingAs a specialized manufacturer, we supply N-Methylacetanilide to global industrial partners who require consistent quality for advanced downstream processing. This intermediate functions primarily in select fine chemicals and specialty segments where stringent process control and proven performance are critical. Below are principal application scenarios categorized by real-world industrial usage, highlighting integration in manufacturing, regulatory benchmarks, and typical end products. 1. Agrochemical Synthesis IntermediatesIn pesticide and herbicide synthesis, formulators use N-Methylacetanilide as a controlled building block for producing certain amide-linked active ingredients. Downstream manufacturers rely on its stable methylated structure for coupling and protection reactions during multi-step organic synthesis. We collaborate closely with agrochemical producers to ensure traceable batch quality from intermediates through to the active compound loading stage. Industry compliance standards
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2. Pharmaceutical Intermediate (API Synthesis)Pharmaceutical manufacturers apply N-Methylacetanilide as a defined intermediate during the multi-step synthesis of several amide-analog APIs, particularly in analgesics and local anesthetic agents. Its use provides both steric protection and selective activation sites. Our production facilities maintain rigorous documentation and in-process QC to conform to cGMP traceability requirements across all API supply chains. Industry compliance standards
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3. Dye and Pigment Intermediate ManufacturingProducers of specialty dyes utilize N-Methylacetanilide as a key amide intermediate for synthesis of particular azo and anthraquinone dye molecules. It functions as a methylacetanilide coupling partner, enhancing shade specificity and solubility in final colorant formulations. Control over purity and residual trace impurities remains essential to deliver stable chromophore properties and textile compatibility. Industry compliance standards
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4. Rubber and Polymer Processing AidIn advanced polymer compounding, especially certain specialty rubbers, downstream processors use N-Methylacetanilide as a polymerization aid and processing modifier, capitalizing on its ability to influence plasticity and chemical structure during synthesis. Our high-conversion, low residual impurity grade supports stable integration, helping improve extrusion or molding characteristics without introducing byproduct contaminants. Industry compliance standards
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5. Organic Synthesis Research ChemicalsResearchers and fine chemical producers routinely include N-Methylacetanilide as a methylated amide substrate in pilot scale and laboratory-scale synthetic explorations, due to its selective reactivity in functional group transformations, including Friedel–Crafts acylations and directed ortho-metalations. Our facilities support customized batch sizes and documentation according to research-grade requirements to facilitate reproducibility in discovery chemistry programs. Industry compliance standards
Typical usage ratio
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In a production hall filled with reactors, analytical balances, and powder flows, not every compound yields the same weight in a manufacturer's eyes. N-Methylacetanilide remains a staple for us because it strikes a practical balance between reactivity, stability, and handling convenience. The chemical world, full of aromatic amides and their derivatives, rarely offers a compound with such a predictable profile for both structure and performance.
The molecule itself features a methylated nitrogen bonded to an acetanilide backbone. This small adjustment—substituting a methyl for a hydrogen on the nitrogen—is responsible for changes in solubility, melting point, and reactivity patterns that matter in real-world synthesis and formulation work. Our daily experience comes not from catalog sheets or abstract data, but from hundreds of batches where temperature, humidity, and solvent choice become deciding factors. In this environment, a crystalline solid that handles well, crystallizes reliably, and measures accurately stands out. N-Methylacetanilide fits that description.
Each time a drum of N-Methylacetanilide fills from the dryer, we check a few things: color consistency, freedom from visible contaminants, and flowability. The material appears as white crystals, with an occasional faint cream tint from tiny process variables—always a cue for closer inspection. Its melting range (just above 88°C in our controlled conditions) sits higher than acetanilide itself, which makes a difference during purification and storage. This physical identity means fewer surprises at crucial production steps, like filtration and drying, when the wrong crystal habit can choke filters or jam augers.
Solubility guides downstream utility. Our records show clear solubility in most organic solvents used in dye and pharmaceutical manufacturing—especially in ethanol, acetone, and chloroform—allowing formulators to avoid pre-dissolution headaches. It resists excessive swelling or lumping in humid air, which shortens cleaning cycles and reduces product loss.
We’ve worked with customers ranging from dye manufacturers to pharmaceutical formulators. In dyestuff synthesis, N-Methylacetanilide serves as a controlled intermediate in the production of azo compounds, where the methyl group on the nitrogen hinders unwanted side reactions, ensuring color purity and minimizing waste. Downstream purification runs more efficiently because its side products prove easier to separate compared with unsubstituted derivatives.
Pharmaceutical projects often leverage this molecule’s specific N-alkyl functionality. It acts as a scaffold, where the subtle differences in hydrogen-bonding and steric bulk help medicinal chemists tweak lead compounds' performance, stability, or enzyme binding. We’ve watched teams replace plain acetanilide with the methyl analogue and reach their analytical targets sooner thanks to improved selectivity in key steps such as acylation, alkylation, and selective functionalization.
Each plant has its quirks—reactor geometry, temperature gradients, recycling protocols. We see consistent product because we marry reliable synthetic routes (starting from high-purity aniline and acetic anhydride, followed by careful methylation) to hands-on quality checks. Moisture content, residual solvents, and trace metal analysis run as routine, with full spectra archived for every batch.
What separates our N-Methylacetanilide from alternatives in trade? We focus not merely on meeting the minimum assay standards (always above 99.5% by GC in finished product), but on purity beyond primary metrics. Experience taught us that trace byproducts—not flagged on a generic COA—can undermine downstream performance, and a dye run ruined by one batch of subpar amide leaves a long memory. We filter, wash, and vacuum-dry with an eye toward batch-to-batch uniformity that operators and downstream users notice.
One rarely appreciated factor: particle size distribution. Finer powders can cake or drift, leading to handling losses, while oversize crystals slow dissolution and dosing. In our process, crystal habit is tuned at the recrystallization stage. That’s why users report smooth charging to reactors—important in automated feed systems, especially where dust scrutiny runs high.
Chemistry abounds with amides, but direct comparisons show the uniqueness of N-Methylacetanilide in everyday processing. Acetanilide itself serves as a building block for many processes, but it exhibits higher reactivity at the nitrogen due to the free hydrogen, impacting the selectivity in certain syntheses. For users scaling up new chemistry, that difference marks the line between a clean, high-yielding conversion and a mess of byproduct separations. We’ve spoken with teams who trialed both compounds before settling on the methylated version for its improved selectivity—particularly in reductive transformations and functional group interconversions.
Compared to other N-alkylated derivatives—like N-Ethylacetanilide or N-Propylacetanilide—the methyl group keeps the molecular bulk low, which maintains higher solubility and process compatibility without introducing excessive hydrophobicity or drastically shifting melting points. We run side-by-side solubility and compatibility checks to guide customer choices, often finding the methyl analogues outperform heavier substitutions, especially in multistep dye syntheses.
Users asking for N,N-Dimethylacetanilide sometimes anticipate similar handling, but this fully substituted amide hydrophobically separates from key solvent systems and runs hotter in exothermic additions. Our repeat customers favor the mono-methylated structure for those very reasons: balanced reactivity and handling.
Nothing influences us more than the run history in plant logs. Over the years, feedback from repeat synthesis, scale-ups, and new product development cycles shaped our confidence in recommending N-Methylacetanilide. Each product batch records actual performance, from filtration rates to observed impurity retention, giving us a working library of process improvements and troubleshooting insights.
Our technical staff regularly visits user sites, walking the lines with operators and quality teams. We see firsthand how N-Methylacetanilide's predictable behavior solves specific problems—blocking unwanted N-acylation side reactions, surviving harsh temperature cycles, forming minimally colored solutions, and avoiding the smoky odors some analogues carry under acidic or basic conditions.
Beyond laboratory test tubes, industrial-scale synthesis puts theoretical advantages into stark relief. Processes involving coupling, diazotization, or cyclization consistently run smoother with well-made N-Methylacetanilide. Take any high-throughput setup in dye or active pharmaceutical ingredient (API) synthesis—less downtime, fewer filter swaps, and less labor wasted on rework stand as markers of the compound’s real value.
Manufacturing chemicals at scale comes with environmental and safety responsibilities. We integrate best practices for waste minimization at each synthesis stage, capturing unreacted aniline and solvent for safe recycling. Our material avoids halogenated contaminants and heavy metal residues, important for disposal and downstream compliance. Over time, optimizing energy use in methylation steps and streamlining purification have cut emissions and improved yields, directly benefiting both plant operators and customers down the line.
We’ve adapted our equipment for closed-system handling and dust control, a response to evolving health standards and direct user input. Customers involved in regulated sectors—such as pharmaceuticals and food dyes—need confidence that their raw materials will not trigger surprise inspections or regulatory hold-ups. Our expertise enables us to audit supply chains, keep certificates up to date, and intervene early in the rare event that trace off-spec problems arise.
Every raw material, no matter how well made, faces challenges. In early days, variable humidity in storage led to minor clumping and measurement loss. After fielding customer complaints, we invested in moisture-scavenging liners and climate-controlled packaging lines. We also reworked shipping logistics, treating transit during peak monsoon months as a special case. Open feedback from users led us to trial new crystal morphologies, ultimately landing on a reproducible, free-flowing product that ships well even to tropical ports.
Another challenge involved batch scale-up. As demand for N-Methylacetanilide increased, we noticed subtle shifts in crystallinity and drying time pushing impurity levels outside our strict targets. Tackling this meant overhauling reactor configurations, implementing segmented cooling, and retraining operators to recognize the right endpoints by both sight and analytical checks. Direct interviews with end-users—at labs and in production—highlighted the need for a consistent melting point and fast, clean dissolving.
User applications in sensitive chemical syntheses brought regulatory scrutiny regarding trace nitrosamine formation and solvent residues. We responded by changing over to low-nitrite water supplies, updating analytical protocols, and investing in newer GC and LC-MS equipment to ensure every batch passes with wide margins.
Nothing defines a product more, from our perspective, than watching it in action in a real production setting. One dye house reported seasonal gelling issues with their previous supplier’s material, leading to clogged feeding hoppers. By shifting to our material, with its narrower crystal size distribution and documented low residual moisture, their line moved from hours lost per week in downtime to near-continuous throughput.
Yet another pharmaceutical partner commented on their struggle with batch-to-batch variance in impurity profiles, which stalled production of a critical active intermediate. By sharing our batch analytics and working with their QA team, we aligned on a spec exceeding industry minimums, with extra reporting on trace byproduct classes. That transparency enabled their regulatory filings to proceed faster, and their own scale-up troubleshooting cut weeks out of their development timeline.
We take pride not just in clean certificates, but in listening closely, walking customer lines, and learning from every unusual occurrence—be it a persistent off-odor, an unexpected melt range drift, or a rare filterability issue. Our cumulative experience flows directly into both better product and user support.
Demand continues to evolve, with more industries seeking bespoke aromatic amides for advanced materials projects. Polymers, coatings, and specialty resins sometimes ask for specific melting points or solubility limits, and N-Methylacetanilide frequently enters the conversation as a versatile base compound.
We work closely with R&D groups piloting new processes, offering pilot-scale quantities and fine-tuning crystal habit, purity cutoffs, and solvent compatibility based on actual feedback from test runs. Early involvement has led to less formulation trial-and-error and helped accelerate commercial rollout for new end products.
Unlike lab-made samples, real industrial lots occasionally surface edge cases—a batch may form dust finer than expected, or specific batches may dissolve a hair slower in cool conditions. Each feedback cycle leads us to tune process controls or storage parameters, constantly driving product improvement.
Over many years, we’ve seen plenty of alternative N-substituted amides trialed for cost or performance reasons. Some facilities started with the idea that N-ethyl or N-propyl variants might offer greater stability or improved downstream reactivity, only to discover handling headaches—difficult feeding, stubborn residues, and erratic purification. N-Methylacetanilide’s modest steric demand keeps it soluble and manageable without sacrificing the desired reactivity in most acylation and condensation chemistries.
With acetanilide itself, we've repeatedly heard about errant side reactions and the headaches of over-alkylation, especially during large-scale dye compound synthesis. Our records show that switching to the methylated derivative often resulted in cleaner product, simpler purification, and greater batch reliability—benefits more keenly appreciated at multi-ton scales where each downtime hour carries a real cost.
As sustainability pressures mount, the demand for efficient and minimal-waste processes makes raw material predictability paramount. N-Methylacetanilide, with its clear track record, predictable solubility, and tightly controlled impurity profile, will continue to anchor a range of key reactions.
Regulatory landscapes will become stricter, especially in pharmaceutical and specialty chemical synthesis. Our ongoing investment in process controls, analytics, and upstream raw material vetting helps users maintain compliance and respond rapidly to evolving standards. Open communication between manufacturer and user—grounded in hands-on experience rather than theoretical claims—remains the key to long-lasting trust.
Manufacturing real chemicals for real-world processes doesn’t leave room for guesswork or “good enough” standards. Our decades of producing, refining, and problem-solving with N-Methylacetanilide reflect a commitment to both quality and partnership. As it finds new uses beyond dyes and pharmaceuticals, we remain ready to innovate alongside the industries that rely on the practical strengths of this workhorse molecule.