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HS Code |
875920 |
| Chemical Name | 4-Acetamidophenylacetonitrile |
| Cas Number | 7466-73-9 |
| Molecular Formula | C10H10N2O |
| Molecular Weight | 174.20 |
| Appearance | White to off-white solid |
| Melting Point | 152-155 °C |
| Solubility | Slightly soluble in water |
| Storage Temperature | Store at room temperature |
| Smiles | CC(=O)NC1=CC=C(C=C1)CC#N |
| Inchi | InChI=1S/C10H10N2O/c1-7(13)12-9-4-2-8(6-11)3-5-9/h2-5H,1,12H2 |
As an accredited 4-Acetamidophenylacetonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Sealed amber glass bottle containing 25 grams of 4-Acetamidophenylacetonitrile, labeled with chemical name, CAS number, and safety warnings. |
| Shipping | 4-Acetamidophenylacetonitrile is shipped in securely sealed containers, protected from moisture and light. It is packaged according to standard chemical safety regulations, labeled appropriately, and typically shipped by ground or air in compliance with international transport guidelines. Handle with care, and ensure delivery to authorized recipients only. |
| Storage | 4-Acetamidophenylacetonitrile should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition, moisture, and incompatible substances such as strong acids or bases. Keep it protected from light and in a designated chemical storage cabinet. Always follow appropriate safety protocols and local regulations for handling and storing chemicals. |
Applications of 4-Acetamidophenylacetonitrile in Industrial ManufacturingAs a direct manufacturer, we supply 4-Acetamidophenylacetonitrile to globally recognized chemical sectors that require precise intermediates for advanced synthesis. This compound supports critical downstream value chains that demand strict compliance with international regulations, consistent batch quality, and industrial-scale integration. 1. Pharmaceutical Intermediate for Paracetamol AnaloguesIn the pharmaceutical synthesis of paracetamol and its structurally related analogues, companies use 4-Acetamidophenylacetonitrile as an acetamide-based building block in multi-step organic routes. Its nitrile group provides a reliable entry point for further transformations, supporting advanced molecule design under tightly controlled GMP environments. Industry compliance standards
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2. Agrochemical Synthesis for Phenylacetamide HerbicidesMajor agrochemical plants use this material as an intermediate in the production of selective phenylacetamide herbicides. The functional nitrile group reacts in targeted transformations, supporting scalable batch operations while ensuring compliance with stringent pesticide regulations. Industry compliance standards
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3. Fine Chemical Manufacturing for Aromatic Amine DerivativesChemical plants focused on specialty intermediates for dyes and advanced polymers incorporate this compound in their aromatic amine synthesis routes. Its reactivity enables efficient growth of molecular complexity in niche fine chemical production lines, supporting demanding quality and traceability requirements. Industry compliance standards
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4. API Impurity Profiling and Reference Standard PreparationLaboratories specializing in impurity profiling during pharmaceutical development use this compound for synthesizing and characterizing trace-level reference compounds. Accurate quantitation supports regulatory submissions and compliance during final drug registration. Industry compliance standards
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Each day on the production line, we handle many specialty chemicals, but few draw as much steady attention as 4-Acetamidophenylacetonitrile. This compound, with its distinct acetamido group and nitrile function, signals its value the moment it’s mentioned in a customer call or R&D inquiry. We keep this material on hand for one reason: research teams and development labs continue to count on it as a key intermediate, especially for pharmaceuticals and advanced materials. Every gram we dispatch supports someone’s innovation or process, and that underscores the significance behind every batch we release.
Manufacturing 4-Acetamidophenylacetonitrile demands a routine we know inside out. Our production uses a batch synthesis built on benchtop chemistry, scaled for industrial demand. Most requests specify our AC-04019 model, which we’ve refined based on years of feedback from medicinal chemists and custom synthesis clients. The off-white to faintly yellow solid, with reliable purity levels reaching 99%, maintains consistency due to quality control routines adapted over time, not just copied from manuals. We refuse to cut corners upstream or skip steps at the reactor just to chase numbers. We have seen that patience during crystallization or solvent adjustment makes a difference later for our clients, especially those setting up follow-up syntheses—often for painkillers, drug candidates, or specialty polymers where trace impurities end up in the spotlight.
Countless aromatic nitriles crowd the catalogs, but our clients return to 4-Acetamidophenylacetonitrile time and again. It’s not an accident. The acetamido motif doesn’t just sit for show; it delivers functional versatility, acting as both a protective group and a synthetically approachable anchor for further transformation. While basic nitriles may offer a quick route for Grignard chemistry or reduction steps, our compound’s amide function opens doors for aminations or more selective coupling. The difference reveals itself in every successful scale-up where process efficiency, selectivity, or downstream purification comes to the fore. Chemists working on new molecule libraries report cleaner reactions and more predictable results when using our tightly controlled batch output, which saves them rerun time and resources.
Years ago, nobody anticipated just how pivotal specialty nitriles would become in complex molecule synthesis, particularly where regulatory standards keep tightening. Our process engineers responded to supply shortfalls in the market by not only boosting output but also developing cleaner workups to address solvent residues. These ongoing changes did not originate in boardrooms but from hours on the plant floor, troubleshooting crystallization, adjusting distillation columns, and working hand-in-glove with in-house analysts. We remember those first months the market threatened an influx of cheap material from traders—batches that failed dissolution or contained organics nobody could trace. Producers with skin in the game know it makes a difference when analytical results tie directly to operator pride, not to paperwork designed for resale.
The stories we hear from the field make the value of our product real. A research chemist once called to share how critical high-purity 4-Acetamidophenylacetonitrile had become in synthesizing novel CNS-active agents. Other clients talk about its role bridging classic benzylic coupling to urea and carbamate formation—steps where minor impurities could torpedo an entire screening program. On the process development front, one partner used a single model lot from our plant and managed to reduce downstream chromatographic steps by half, based on cleaner product isolation.
Some synthetic routes just don’t budge without the specific combo of phenylacetonitrile backbone and acetamido protection. For generic manufacturers, producing intermediates for acetaminophen analogs or specialty dyes, margins remain thin. Poorly formed acetanilide impurities send them scrambling for rework. It’s these details—real-life headaches avoided—that drive our decision to focus on making every delivery dependable.
Plenty of alternatives exist: simple benzonitriles, acetanilides, plain acetonitrile derivatives. But whenever cost-cutting pushes a change, clients experience tangible setbacks. Basic nitriles don’t carry the same reactivity, especially when coupling with sensitive amines or during palladium-catalyzed steps. Even among substituted versions, only the acetamidophenylacetonitrile provides the needed chemical grip for dual-function transformations. Our records show most repeat customers once tried a cheaper variant, only to cycle back after failed conversion or downstream color issues. We’ve watched as production managers check post-reaction TLCs and report sharper spots using our product, meaning purification comes easier and yield loss drops off.
Some user feedback centers on melting point consistency as a quick purity check. Unstable grades from traders often turn waxy or require forced drying, introducing risk into finely tuned operations. Our on-site batch records tie together lab data and production notes. That’s one reason users in regulated spaces, especially those stuck with incomplete batch documentation from resellers, opt to go back to a direct producer for next orders. We know these challenges; many of us started in bench roles before scaling up.
Over time, industry standards moved. Early days saw basic purity as the benchmark, but client demands expanded. Now, careful documentation of source, full spectra verification (NMR, HPLC), and minimal residual solvents have become standard expectations. Every batch goes through an array of post-synthesis checks, not out of routine but in direct response to customer conversations and prior audit outcomes. As regulatory requirements changed, especially for those producing APIs downstream, we updated not just our testing profiles but internal record keeping. Our analysts work shoulder-to-shoulder with production, ensuring feedback translates into every cycle.
Our approach reflects daily realities. In-house teams vet each step, from raw materials to packaging. Process optimization didn’t stop with the original flow chart—every issue that showed up in a customer’s reaction flask sparked further adjustment. Overhearing a frustrated chemist say, “The material last month was spot on,” told us more than generic satisfaction scores ever could. Our pride rests on real metrics: NMR spectra overlay, reactivity in model couplings, and long-term customer retention—not marketing claims.
Reliable access to consistent 4-Acetamidophenylacetonitrile lets our customers focus on their core innovation. We’ve noticed that disruptions—whether due to global shipping slowdowns, inconsistent intermediates, or questionable documentation—hit R&D teams the hardest. Production chemists feel the sting in missed deadlines, while QC managers spend hours tracing the source of unknown peaks. Down-to-earth communication with our users puts us in their shoes. We share their frustration over nonconforming shipments and intermittent off-spec batches. These experiences feed back into our process design, fostering batch-to-batch repeatability, stability studies under varied warehouse conditions, and clear, no-nonsense analytical summaries.
One major lesson: transparent handling of minor specification deviations earns trust, provided the data stays robust and traceable. Our teams catch issues before they reach a customer’s lab, but if a question comes up post-delivery, we have batch records at the ready—no paper trail dead-ends. This openness with users formed out of necessity, not because an audit says so, but because real production setbacks taught us how much a single impurity ruins days of work down the line.
Chemists and technical purchasers grow weary of the “gray zone” that surrounds chemical resellers. Products circulate with uncertain origins and paperwork claims that barely stand up to scrutiny. Over the years, customers have brought us samples from alternative sources, asking for an honest assessment. Lab comparisons repeatedly show off-target elemental analysis, unexpected side products, and occasionally, batch-to-batch variation that scrambles downstream processes. Direct manufacturing keeps these challenges at bay. No rushed relabeling or speculative purity. Every shipment stems from our facility, controlled by people who actually run and adjust the reactors, not just ship boxes.
We learned long ago that chemists notice the difference between hand-checked product and logistics quick fixes. Often, quality slip-ups show up under the radar: smudged spectra, unknown solvent residues, or color instability in stored lots. Producers who own their process have a different incentive structure—no temptation to pass off a problem batch or mask inconsistency behind vague paperwork. We keep correcting our procedures based on season, humidity, even the type of drums used for final packing, because each of these factors feeds into the reliability we want to guarantee.
No raw material stays perfect for every use case. 4-Acetamidophenylacetonitrile excels as a building block in medicinal chemistry and select advanced materials, where the precise introduction of an acetamido group combined with the activation at benzylic positions becomes critical. That said, users pushing far outside typical pharmaceutical or chemical synthesis areas may find better matches among other phenyl derivatives, especially if their process requires alternative leaving groups or specific functional protection strategies. But for the core clientele—those driving medicinal programs or transferring R&D concepts to the plant scale—the material’s qualities align tightly with routine needs.
Some users mention that on rare occasions, reactivity with unusually aggressive reducing agents prompts formation of off-pathway byproducts. We keep up with such findings by supporting customers’ troubleshooting, offering insights gained from our own scale-up experiments, and—if warranted—tuning crystallization or solvent traces for tighter conformity. Where possible, we pass along findings and modified best practices to client support teams, closing the loop between field feedback, plant procedure, and analytical refinement.
Shifts in global attitudes and local compliance expectations affect every batch. Our company maintains ongoing evaluation of raw materials, solvent usage, and waste reduction. Integrated environmental controls, including recovery of solvents and energy-efficient heating, mark steady changes each year. Regulatory compliance in the space remains complex, but we take experience from audits—whether related to pharmaceutical regulation, occupational safety, or environmental policies—and bake findings back into our process. Long before it became industry trend, we made the move to cleaner handling and full traceability, not “because it looks good” but because lessons learned from remediation and incident reviews hammer home the costs of shortcutting these critical areas.
Routine in-plant safety and hygiene standards shape not just worker well-being but influence final material quality. Many days, the line between a clean, well-ventilated work site and a downstream impurity originates in these unseen routines. Not every lot may impress by appearance alone, but we know stability and absence of trace organics set the floor for successful synthesis, especially as regulations bite down harder each year. We keep talking openly to local inspectors and industry bodies, staying honest about what works, what proved troublesome in practice, and what we’re changing to meet the next decade’s worth of requirements.
After years of shipping this key intermediate, our collective experience sharpens focus on what truly matters to end users. Beyond the CAS number, it’s the tight control over both process and people that makes each batch dependable. Clients reward that commitment with loyalty, not because a label says so, but because failed syntheses and wasted effort elsewhere show the value of direct, accountable supply. Every process bottleneck or problem batch teaches us where to target improvements—from batch record clarity to practical post-delivery troubleshooting.
We keep investing in process improvements, training operators, and upgrading in-house labs. The gains might not always appear on a glossy datasheet, but our partners notice them when a shipment turns up exactly as expected, with every spectral comparison and reaction test lining up. They value having someone in production who knows what failure looks like, who takes calls after hours to talk through a stalled synthesis, and who pushes forward with the tweaks and upgrades no one asks for on paper.
Chemicals like 4-Acetamidophenylacetonitrile link together the work of scientists, engineers, and process managers. Value in this compound doesn’t come from market volume or catalog size, but from dedication to the small advances behind every order: reducing off-target impurity formation, delivering paperwork that holds up to inspection, and providing a steady hand when troubleshooting gets complex. Our operation thrives not just because we ship plenty, but because those who rely on us for this intermediate drive their own success off our daily attention to the details.
What we bring to the table is not just a product, but a working relationship. Whether it’s accommodating a rush timeline, splitting shipments into specialty packs, or simply talking through a tricky scale-up—these touches carve out an edge for teams working against tight budgets and tougher chemical challenges. We keep an open line to the labs and plant floors worldwide where our product ends up, and an ear to emerging technical needs.
We see firsthand how industry’s ambitions rest on dependable, traceable chemicals. 4-Acetamidophenylacetonitrile, in our experience, stands as a finely honed tool for those aiming to push boundaries in therapeutics, smart materials, and synthesis innovation. Decades of handoffs, audit reports, and shift changes at the production line haven’t dulled our attentiveness to what actually matters—getting the right material, on time, with every technical expectation met or exceeded.
As a manufacturer, we anchor our standards in direct feedback from hands-on chemists and plant operators, not from catalog summaries or broad promises. That’s what sustains our supply chain’s real value, batch after batch, ensuring each client’s project stands on solid ground, supported by reliability forged through years of production floor experience.