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N-Acetyl-2-Phenylethylamine

    • Product Name N-Acetyl-2-Phenylethylamine
    • Alias Acephenyl
    • Einecs 629-019-4
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    942708

    Chemical Name N-Acetyl-2-Phenylethylamine
    Cas Number 4676-35-1
    Molecular Formula C10H13NO
    Molecular Weight 163.22
    Appearance White to off-white solid
    Melting Point 71-75°C
    Boiling Point 312.0°C at 760 mmHg
    Solubility Slightly soluble in water, soluble in organic solvents
    Density 1.09 g/cm³
    Purity Typically ≥98%
    Synonyms N-Acetylphenylethylamine, Acetyl-β-phenylethylamine
    Storage Condition Store at room temperature, in a dry and well-ventilated place
    Smiles CC(=O)NCCc1ccccc1
    Inchi InChI=1S/C10H13NO/c1-9(12)11-7-8-10-5-3-2-4-6-10/h2-6H,7-8H2,1H3,(H,11,12)

    As an accredited N-Acetyl-2-Phenylethylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle with tamper-evident cap, white label displaying "N-Acetyl-2-Phenylethylamine, 25g, ≥98% purity, Store cool, CAS: 27819-91-8".
    Shipping N-Acetyl-2-Phenylethylamine should be shipped in tightly sealed containers, protected from moisture, heat, and direct sunlight. It must be handled in accordance with standard chemical safety regulations and labeled appropriately. Ensure compliance with local, national, and international transport guidelines for chemical substances. Avoid physical damage during transportation.
    Storage Store N-Acetyl-2-Phenylethylamine in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area. Keep away from incompatible substances such as strong oxidizers and acids. Clearly label the container and ensure it is stored according to chemical safety regulations. Access should be limited to trained personnel wearing appropriate protective equipment.
    Application of N-Acetyl-2-Phenylethylamine

    Applications of N-Acetyl-2-Phenylethylamine in Industrial Manufacturing

    N-Acetyl-2-Phenylethylamine finds targeted use in select sectors due to its unique functional properties and compliance with strict quality management guidelines. As a producer with direct manufacturing capabilities, we address the needs of each application by providing consistent specification control and guidance aligned with regulatory frameworks. Below are key industrial scenarios where this material plays a crucial role in formulating differentiated finished goods.

    1. Pharmaceutical Intermediate for CNS-Active Compounds

    Manufacturers of central nervous system (CNS)-modulating agents integrate N-Acetyl-2-Phenylethylamine as a building block in synthesis routes for various therapeutic actives. Its stable acetyl group improves handling and consistent results during multi-step chemical transformations, particularly in selective acetylation or N-alkylation steps when targeting phenethylamine-based APIs. Production environments must rigorously uphold regulatory requirements pertaining to traceability, impurity profiles, and validated synthetic methods to supply the pharmaceutical market.

    Industry compliance standards

    • Good Manufacturing Practice (GMP) as defined by ICH Q7 guidelines
    • International Pharmacopoeias (USP, EP, JP monographs where relevant)
    • 21 CFR Part 210/211 (US FDA)
    • Regulations of Drug Master Files (DMF) for intermediates (where required)

    Typical usage ratio

    • 0.8–1.5 molar equivalent relative to target substrate in synthesis batch; exact amount based on stoichiometry and by-product minimization

    Downstream process integration

    • Used in solution phase synthesis—typically added after pre-activation of phenylethyl group or during reductive amination; followed by purification, crystallization, and analytical quality checks prior to release to API production

    Final product types

    • CNS-active drug intermediates
    • Final Active Pharmaceutical Ingredients (APIs) containing acetylated phenethylamine scaffolds
    • Specialty small-molecule pharmaceutical actives

    2. Fragrance Intermediate for Fine Chemistry

    Fine fragrance compound producers utilize N-Acetyl-2-Phenylethylamine in customized aromatic derivatives, prioritizing product reproducibility and formulation transparency. Its mild aromatic character and modifiable acetyl group enable downstream chemists to build olfactory notes or create fixatives through specific acylation and condensation processes. Continuous in-process checks and compositional purity are critical for downstream blending and regulatory labeling.

    Industry compliance standards

    • International Fragrance Association (IFRA) Standards
    • EU Regulation (EC) No 1223/2009 for cosmetic ingredients
    • IFRA/IOFI Labeling Manual
    • ISO 9235:2013 (Aromatic Natural Raw Materials—Definitions)

    Typical usage ratio

    • 0.1–0.3% of total fragrance batch; adjusted depending on target aroma intensity and regulatory residue thresholds

    Downstream process integration

    • Introduced during intermediate stage synthesis of aroma chemicals—post-reacted, isolated, then incorporated into final fragrance oil blending under controlled conditions

    Final product types

    • Complex fine fragrance bases for perfumery
    • Industrial and personal care fragrance compounds
    • Functional aromatic additives for consumer products

    3. Nutraceutical and Food Additive Precursor

    Food ingredient manufacturers apply N-Acetyl-2-Phenylethylamine as a controlled-source precursor during the synthesis of certain dietary supplement intermediates and flavoring agents. Careful management of purity, cross-contaminant absence, and trace-level quantification are mandated for downstream acceptance, as additive regulations vary globally. Each batch undergoes comprehensive food safety and compliance review before inclusion in consumable products.

    Industry compliance standards

    • Food Chemicals Codex (FCC)
    • Regulation (EU) No 1333/2008 on food additives
    • US FDA 21 CFR 172/182 (where permitted)
    • ISO 22000 Food Safety Management Systems

    Typical usage ratio

    • 0.01–0.08% weight of the processed food or dietary supplement component; level adapted to reach required flavor or precursor function while maintaining below established safety thresholds

    Downstream process integration

    • Added during controlled synthesis or encapsulation of dietary functional ingredients; strict in-line QC controls, then delivered to bulk food or health supplement blending

    Final product types

    • Precursor compounds for functional dietary supplements
    • Encapsulated flavoring agents
    • Food ingredient blends for nutrition bars or beverage powders

    4. Specialty Monomer for High-Performance Polymer R&D

    Advanced polymer researchers in the electronics and specialty coating industries utilize N-Acetyl-2-Phenylethylamine to introduce modifiable aromatic units in custom polymer backbones. The acetyl group facilitates subsequent cross-linking or controlled deprotection in processing, enabling production teams to meet demanding electrical or barrier performance targets. Regulatory grade documentation and batch traceability ensure compliance in pilot and scale-up phases.

    Industry compliance standards

    • ISO 9001 Quality Management System
    • RoHS Directive (2011/65/EU) for electronic material restrictions
    • REACH Regulation (EC) No 1907/2006 for chemicals in polymers (Europe)
    • UL 94 Flammability Standard (where final application requires)

    Typical usage ratio

    • 1–7% by weight in specialty co-monomer blends, precisely adjusted based on target polymer properties and measured downstream reactivity

    Downstream process integration

    • Charged into pre-polymerization setup with primary monomers; followed by high-temperature polymerization, and process monitoring for degree of functionalization and compositional uniformity before downstream finishing

    Final product types

    • Specialty polyamides and polyimides for electronics encapsulation
    • Coating resins with enhanced aromatic content
    • Functionalized polymers for R&D and pilot-scale electronics materials
    Free Quote

    Competitive N-Acetyl-2-Phenylethylamine 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 sales7@sinochem-nanjing.com.

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    Tel: +8615371019725

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    Certification & Compliance
    More Introduction

    N-Acetyl-2-Phenylethylamine: Direct from the Manufacturer’s Floor

    What Sets Our N-Acetyl-2-Phenylethylamine Apart

    Every batch of N-Acetyl-2-Phenylethylamine rolling out from our reactors gets the full treatment: our techs track every detail from raw material sourcing to final crystallization. We moved to closed-system acetylation several years back, locking down contamination risks and tightening up yield consistency. This isn’t just talk—our oldest customers remember the days before digital sensors watched every reaction, when a small shift in ambient humidity meant adjusting for crystal form by hand. These controls help us hit single-digit ppm on related impurities lot after lot, not because some inspector asks for it but because our customer’s product lines depend on it.

    The acetylation step itself might look simple in a flow diagram—ethylamine, phenylacetic acid, acetic anhydride, and a tuned catalyst system—but anyone on the line knows those are just words on paper. What matters is how those reactants behave during the shift, which intermediates want to run away on you, and where to catch them without wasting time or hiking up solvent loads. Early on, we realized that slow filtration just bottles up everything downstream; now we keep particle control tight right out of the reactor. This is less about cutting costs and more about making sure the purity tests match the printout every time. End users tell us this makes the difference when products upstream begin to gel or throw off-color hints.

    Batch Consistency: Not Just a Buzzword

    Our repeat buyers, especially those in fine chemicals or custom synthesis, have poked plenty of holes in generic “consistent quality” claims over and over. You can’t stuff off-spec product into a customer’s drum and blame a “challenging reaction”—not if you want to see next season’s order. In one case, a client ran parallel stability studies on five lots from five sources. Only ours stayed predictable across freeze-thaw cycles and long-term storage at high humidity, thanks to real attention to trace moisture and particle morphologies. It’s easy to tweak a process to hit a purity target once; holding that bar across months of production, through seasonal shifts and feed variations, takes boots-on-the-ground troubleshooting at scale.

    Any manufacturer working with N-Acetyl-2-Phenylethylamine sees the typical issues: stickiness on drying, minor color changes after extended storage, sensitivity to surface contact. We run forced-aging tests in real-world packaging that mimics how our customers store the product—no fancy conditions, just regular, rough treatment. The residual solvent figures, reviewed every week by our in-house team, tie directly into bulk storage specs, so our partners get the same material at the start as the end of the contract.

    Model, Specifications, and What Matters in Real-World Use

    We keep our model codes simple and assignment based on the route of synthesis, not just on minor analytical specs. Finer crystal fractions go into lots aimed at chromatographic applications, while bulk grades—still running high-purity—target intermediates where filtration rates and ease of dissolution matter more. We learned by collaborating directly with downstream operators who watch every minute they lose mixing clumps or filtering through sticky masses. Powder flow rates have turned into more than just numbers—they define how long lines keep moving and how much yield customers actually get. Particle size distribution is measured, tracked, and tuned to meet the practical needs of those pulling from drums, not just those running NMR scans. Mostly, users care about how it handles: how well it re-dissolves, whether it puts stress on their glassware or reacts unpredictably to heat.

    Specifications aren’t locked purely by tradition. Over the years, feedback pointed to new trace analytical requirements—maybe a volatile solvent the regulatory landscape now restricts, or an emerging impurity causing skin sensitivity in the workplace. We keep certificates transparent, updating ranges and issuing addenda with full traceability, and we do so because audits aren’t just paperwork exercises. Some of our earliest custom clients have since shifted to different end uses, but they still call in for a technical refresh or batch review before ramp-up. The best feedback often comes months after the first drum leaves our gate—the true picture of whether we’re on target.

    Real-World Usage: Following the Product Beyond the Factory Gate

    Most buyers come to us with a clear outcome in mind—another synthesis, a key step in a pilot line, or a specialty additive for advanced materials. We’ve watched our N-Acetyl-2-Phenylethylamine flow into projects all over, from specialty polymerization to reactive amide coupling and even select fields in fragrance chemistry. The feedback loop from those who handle the product every day ends up shaping how we approach process tweaks and quality upgrades.

    Sometimes change isn’t dramatic. A small improvement in filtration time lets a customer shave off hours in downstream processing. Adjusting to a feedback about a faint off-odor led us to swap out cleaning agents and introduce a neutral-air drying step that kicks out subtle volatiles. The impact isn’t always seen at our end, but it shows up where it matters: in fewer complaints, more reorders, and real-time user satisfaction. Once, an operator pointed out a repetitive static buildup during transfer. We tweaked the grind and humidity control; the complaints stopped, and the switch stuck. This is the tempo of constant improvement.

    The Differences That Matter: N-Acetyl-2-Phenylethylamine Versus Other Amines

    On paper, N-Acetyl-2-Phenylethylamine seems a close cousin to straightforward 2-phenylethylamine, but users familiar with both notice where things split in practical terms. N-acetylation calms the profile: volatility drops and storage hazards ease up. While pure 2-phenylethylamine can give off caustic, sharp aromas and readily fuse to packaging, our acetylated grade arrives and leaves stable, crystalline, and without soaking into container linings.

    For those mixing with other amines or running condensation reactions, the differences show up in reactivity. N-Acetyl-2-Phenylethylamine resists side reactions that would otherwise derail yields. It won’t result in runaway polymerization at the conditions where free amines kick up. Years ago, a customer switching over from plain 2-phenylethylamine wanted assurance their new synthetic route would hold together through scale-up; the acetyl derivative stepped in, delivered selective coupling, and dropped their side-product content below even optimistic projections.

    Other alternatives, including unsubstituted amines or N-methylated versions, offer their own selling points—but none produce the balance of manageable handling, target reactivity, and comfort for plant workers that our N-Acetyl-2-Phenylethylamine achieves. The acetate protects the amino group for as long as necessary but sacrifices none of the backbone reactivity down the line. Our experience suggests that simple changes in bulk handling and the choice of derivative impact not just product outcome but full safety audits and equipment life.

    Supporting Claims with Traceability and Results

    Trust builds slowly in chemical manufacturing. Our process logs stretch back more than a decade for core customers. They want numbers behind our words—retained GC/MS files, cross-referenced HPLC for each batch, full tracking of solvent batches, even lot-specific environmental exposures recorded at production points. Batch traceability isn’t just for click-through reassurance but keeps both sides accountable when questions pop up months or even years after use. One research firm raised a concern about a minor tail in their chromatogram; since every batch profile stored long-term, we found date-matching evidence for a spike in feedstock impurity, isolated the event, and closed the loop with upgraded supplier screening.

    On-site audits don’t scare us. Most are welcome chances to demonstrate how tightly we keep process deviations in check, and how closely we fix any root causes. One recent CLP-compliance update from a customer led us to overhaul an auxiliary solvent stream. We pulled together staff across the day shift, mapped the solvent path, and published key adjustments. Rarely does paperwork itself prompt a change; it’s the face-to-face walkthroughs with technical and quality staff that push us to dig underneath normal operations and spot blind spots.

    Documentation only matters if it connects to real experience. Our team’s kept a steady curve of analytical upgrade—bring in new chiral columns, set higher detection standards for minor residuals, and train up process techs to catch off-trend samples. This stretches far beyond chasing the next certificate—it’s about never being satisfied when materials touch hundreds of hands along the full value chain.

    Challenges in Manufacturing and Handling

    The path from raw benzene derivatives to a well-packed drum of N-Acetyl-2-Phenylethylamine isn’t a matter of turning valves and loading tanks. Each batch carries the risk of runaway side-reactions or uncooperative solid formation; hot spots in the reactor mean more rework and less clean product. One year, an unexpected spike in a trace impurity disrupted downstream user runs for weeks—turns out, a small drift in reactor temperature was all it took. Fixing meant looping technical, analytical, and production together, tracking the error to a controller relay swap, and finally folding that experience into future preventive checks.

    Storage and shipment bring their own puzzles. N-Acetyl-2-Phenylethylamine resists a lot of typical degradation routes, but high humidity can slowly push surface clumping or slow melting. We switched to lined drums and tamper-sealed bags, and found that this change alone cut return rates and stopped almost every complaint of shipment “bloom” or off-color surfaces. Friendships with good logistics firms help, but nothing swaps for proper internal loading and clear, double-wrapped closure protocols.

    Down-to-Earth Solutions to Daily Problems

    The most common questions from the field aren’t about theory—they’re about preventing clogs, getting a good pour, speeding through-dissolution, and avoiding headaches over mystery films in finished products. Our plant’s calendar fills with notes from end users, not just distributors, asking for tweaks or sharing pain points. In one situation, repeated chipping from glass bottles during storage came back to rough pour techniques on-site. We changed the grind specs and offered a walkthrough with new transfer kits—the problem evaporated. The source of answers usually lies in the small details, not grand process overhauls; the best solutions fit how the customer already works.

    We don’t chase buzzword compliance; instead, standards emerge from the back-and-forth grind of real needs. Each time a new application shows up—a fresh pharma intermediate, an upstream additive, a pilot-scale custom molecule—we add it to the map, feed findings back into the plant, and build better documentation. Rather than waiting on the regulatory climate to change, we keep voluntary samples cycling through third-party labs and participate in open-data sharing with trusted partners. Direct access to barcoded sample libraries and “trouble lot” histories keep us honest and ready whenever someone needs proof of origin or additional data.

    The Road Ahead: Getting Better with Every Batch

    No chemistry stands still. End uses shift as customer targets evolve, regulations tighten between quarters, and new synthetic approaches demand fresh grades or different carrier systems. We see these as chances to layer in better environmental profiles—less waste solvent, smaller footprints, more streamlined energy for automated lines—without losing the benchmark purity and performance our users demand. In practice, switching up an isolation step or dry-off routine often comes down to end-user trial and error; once we get a process improvement that sticks throughout the supply chain, we document, repeat, and share those gains.

    Staff knowledge carries a lot of weight. Turnover remains low across our plant, so lessons from old bugbears—the usual hangups with batch dissolution, accidental mixing errors, or packaging quirks—don’t get lost. Each problem that crops up in bulk orders or sample runs gets logged and, if needed, passed on by phone, not just email. In this space, keeping relationships personal, suppliers candid, and communication honest beats box-ticking compliance every time.

    We keep an eye on both global supply dynamics and local realities. Raw materials often shift in purity profile or cost, so long-term contracts and alternative sources protect against sudden outages or price jumps. During a recent global shipping bottleneck, planning ahead helped us avoid extended outages that pushed others to desperation pricing. Customers using our N-Acetyl-2-Phenylethylamine didn’t experience dramatic price whiplashes or chaos in delivery timelines—because redundant sourcing and live production calendars earned their keep.

    Quality, Traceability, and Service in Every Shipment

    Manufacturing N-Acetyl-2-Phenylethylamine goes beyond just meeting a target purity level or ticking through a checklist of physical properties. We back each shipment with a real history, recalling batch notes, plant conditions, and feedback results from those who blend the compound every day. If technical teams ask for more analysis, we open our books to them; if customers meet a new regulation, we work side-by-side to cross every “t” without selling short on performance.

    We believe this compound delivers because our users—small batch firms, tech upstarts, established R&D teams—trust us enough to tell us what works, what fails, and what needs more legwork. Bridging the gap between what folks need in the lab or plant and what chemistry can offer in practice means spending as much time listening as pushing new process improvements. N-Acetyl-2-Phenylethylamine will evolve, and so will our approach, built on the kind of honest feedback and hands-on partnership that brings out the best in both the chemistry and those who use it every day.