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4-Acetamidobenzaldehyde

    • Product Name 4-Acetamidobenzaldehyde
    • Alias 4-Formylacetanilide
    • Einecs 211-658-0
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    766434

    Cas Number 1443-80-7
    Molecular Formula C9H9NO2
    Molar Mass 163.18 g/mol
    Appearance White to off-white solid
    Melting Point 161-163 °C
    Density 1.24 g/cm³ (estimated)
    Solubility In Water Slightly soluble
    Chemical Structure C1=CC(=CC=C1C=O)NC(=O)C
    Synonyms p-Acetamidobenzaldehyde; 4-Formylacetanilide
    Iupac Name N-(4-formylphenyl)acetamide

    As an accredited 4-Acetamidobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 4-Acetamidobenzaldehyde, 25g: Supplied in an amber glass bottle with safety cap, clearly labeled with chemical name, formula, and hazard warnings.
    Shipping 4-Acetamidobenzaldehyde is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is typically packed in sturdy, leak-proof bottles or drums with appropriate labeling. The product is handled according to hazardous chemical regulations and transported under ambient conditions, avoiding exposure to extreme temperatures or direct sunlight.
    Storage 4-Acetamidobenzaldehyde 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 oxidizers. Protect the chemical from moisture and direct sunlight. Ensure appropriate labeling and keep the storage area equipped with suitable spill containment and fire control measures.
    Application of 4-Acetamidobenzaldehyde

    Applications of 4-Acetamidobenzaldehyde in Industrial Manufacturing

    As an original producer of 4-Acetamidobenzaldehyde, we support a range of specialized industries that incorporate this intermediate in regulated downstream chemical synthesis. The following scenarios reflect established, commercially validated uses of this material within fine chemicals, pharmaceuticals, pigments, and related manufacturing sectors.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Antibacterial Agents

    4-Acetamidobenzaldehyde serves as a key building block in the synthesis of certain sulfonamide-based antibiotics, particularly within multi-step processes for developing intermediate compounds geared toward regulated API manufacture. Controlled introduction during condensation and subsequent transformation procedures ensures precise molecular architecture and compliance with quality-by-design principles. Manufacturers rely on validated analytics to manage impurity profiles and batch traceability.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP/NF Monographs for intermediate verification
    • EU Guidelines for Good Manufacturing Practice for Medicinal Products for Human and Veterinary Use, Part II
    • Chinese Pharmacopoeia standards for intermediate quality control

    Typical usage ratio

    • Applied at 0.5–1.2 molar equivalents depending on the target API and batch scale; stoichiometry adjusts according to reaction efficiency and impurity tolerances

    Downstream process integration

    • Enters reaction at the condensation stage as an aldehyde substrate for further derivatization
    • Subjected to purification before coupling and final crystallization steps
    • QC batch release prior to API finishing

    Final product types

    • Sulfonamide antibiotics
    • Aromatic amine intermediates for pharmaceutical synthesis

    2. Dye and Pigment Intermediate for Specialty Colorants

    Manufacturers integrate 4-Acetamidobenzaldehyde to synthesize benzaldehyde-based chromophores for pigment and dye production, particularly for disperse and acid dyes. The precise introduction into azo coupling reactions enables the development of high-purity colorant intermediates with specific shade and fastness properties, meeting textile and plastics sector demands. Purification routines maintain color intensity and batch uniformity.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex IV for harmful substances in dyes
    • REACH (EC No 1907/2006) Annex XVII restrictions for aromatic amines
    • EN 71-3:2019 (Safety of Toys – migration of certain elements) for colorants in finished goods
    • ISO 105 Series (Textiles – Tests for colour fastness)

    Typical usage ratio

    • Ranges typically from 3–10% by weight in precursor charge, depending on required chromophore density and shade target

    Downstream process integration

    • Used in initial diazotization and subsequent coupling steps to build aldehyde-based azo dyes
    • Incorporated before final dye purification and granulating or spray-drying procedures

    Final product types

    • Disperse dyes for polyester fiber coloring
    • Acid dyes for nylon and wool
    • Specialty pigment dispersions for plastics and inks

    3. Fine Chemicals Synthesis for Flavors and Fragrances Industry

    This aromatic aldehyde provides an essential functional moiety for the preparation of fragrance intermediates, particularly as a precursor to substituted benzyl derivatives. Integration within controlled multi-step syntheses, including acetalization and reduction to corresponding alcohols, enables formulation of high-purity ingredients used in compounded fragrances. Adherence to food additive codes and allergen listings is maintained throughout all production stages.

    Industry compliance standards

    • IFRA Standards for fragrance ingredient purity and restrictions
    • EU Regulation (EC) No 1334/2008 on Flavorings
    • US FDA 21 CFR Part 172 (Food Additives Permitted for Direct Addition to Food for Human Consumption)
    • ISO 9235:2013 (Aromatic Natural Raw Materials – Vocabulary)

    Typical usage ratio

    • Formulation typically uses 1–4% by weight as a starting aromatic aldehyde in batch charge, with precise ratio optimized for target molecule yield and olfactory purity

    Downstream process integration

    • Introduced in acetalization, reduction, or condensation reactions for key fragrance intermediates
    • Followed by distillation and fractionation to isolate finished components

    Final product types

    • Substituted benzyl alcohols and acetals for fragrance use
    • Functionalized aroma chemicals in compounded perfumes
    • Flavors for use in food and beverage applications

    4. Agrochemical Synthesis Intermediate (Herbicide Precursors)

    In regulated agrochemical manufacturing, 4-Acetamidobenzaldehyde functions as a key reactant for building up aromatic core structures present in selective herbicides. Sequential reactions include aldol condensation, cyclization, and selective reduction or acylation, underpinning production of effective crop protection active molecules. Upstream supply meets GLP and environmental risk standards for integration into registered plant protection products.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP) (ENV/MC/CHEM(98)17)
    • EU Regulation (EC) No 1107/2009 concerning the placing of plant protection products on the market
    • US EPA 40 CFR Part 158 – Data Requirements for Pesticides
    • ISO 9001:2015 Quality Management Systems for agrochemical production

    Typical usage ratio

    • Charged at 0.8–1.4 molar equivalents in initial synthesis, with ratio adjusted for specific active ingredient targets and target synthesis scale

    Downstream process integration

    • Added at core condensation or cyclization step to form substituted aromatic systems
    • Pre-treated for purity, then purified at intermediates stage before integration with other actives

    Final product types

    • Aromatic herbicide active compounds for cereal and broadleaf weed Control
    • Registered active ingredient intermediates for branded formulations

    5. Specialty Polymer Additive Component (Cross-Linking Agent Precursor)

    Polymer manufacturers use this compound within syntheses to prepare aromatic cross-linkers and modifier segments for specialty resins. During staged polymerization, the aldehyde function reacts with diamines or polyols to introduce thermally stable linkages, influencing resin performance characteristics such as heat resistance and curing profile. All steps follow industrial cleanroom and materials registration standards.

    Industry compliance standards

    • ISO 9001:2015 certified production environment
    • EU REACH Regulation Annex XIV for use of aromatic derivatives in polymers
    • UL 94 Flammability Ratings for finished resin components
    • ASTM D638-14 for mechanical testing of polymer samples

    Typical usage ratio

    • Typically introduced at 2–6% by molar ratio with respect to total monomer system, ratio determined by desired cross-linking density and final performance

    Downstream process integration

    • Fed during pre-polymer formation, followed by curing in presence of hardener or catalyst
    • Monitored for homogeneity and residual aldehyde content

    Final product types

    • Specialty thermosetting resins for electronics
    • Structural adhesives with enhanced thermal properties
    • Cross-linking agent concentrates for industrial composite production
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    Certification & Compliance
    More Introduction

    4-Acetamidobenzaldehyde: Real-World Manufacturing, Real-World Advantages

    Understanding What We Make—And Why It Matters

    Anyone who steps into a lab, whether in pharmaceuticals or fragrances, soon runs into the need for solid intermediates. As a manufacturer with two decades shaping aromatic chemistry, we’ve worked hard to make sure 4-Acetamidobenzaldehyde stays off the problem-list for our partners.

    What sets this molecule apart isn’t just its functional groups or structure. To us, its true value comes from how reliably it helps chemists reach their target compounds, and how it manages to bridge gaps other aldehydes often leave. Over years, watching dozens of process engineers and scientists navigate tricky syntheses, it became clear why 4-Acetamidobenzaldehyde continues to hold its own amid a field of alternatives.

    Our Product: Model and Core Properties

    We manufacture 4-Acetamidobenzaldehyde under a system designed to favor quality from batch to batch. Our model typically features a purity benchmarked at 99% by HPLC, though in some lots, that mark nudges a bit higher—which matters to chemists requiring precision in downstream reactions. The material itself appears as an off-white to light beige crystalline solid. Melting points sit consistently in the expected 148–151°C range.

    On the analytical side, our in-house QC notes NMR and IR spectra that reflect crisp para-substitution, along with unambiguous signals from the aldehyde and acetamido groups. That cuts out guesswork for those who depend on clean reaction profiles and want to avoid sidesteps due to impurities.

    Where Chemists Put It to Work

    Pharmaceutical scaleups often rely on intermediates that don’t balk under tough conditions. 4-Acetamidobenzaldehyde takes the heat (and acid, and base) in multi-step syntheses. We’ve supplied kilo quantities for runs aimed at making paracetamol derivatives and specialty APIs, with feedback echoing the same theme: consistent conversion, no surprises from the starting material.

    Not every aromatic aldehyde allows the same flexibility. Some competitors have seen customers try meta- or ortho-substituted variants from elsewhere, only to hit roadblocks with selectivity and handling. 4-Acetamidobenzaldehyde’s para positioning, together with the acetamido group, throttles undesirable side reactions while directing clean transformations through processes like condensation or reductive amination.

    It moves beyond pharma, too. Years ago, a customer in the dye industry flagged that our product’s reactivity made it ideal as a coupling component in azo dye synthesis. From personal experience: earlier in my career, I watched R&D teams work through obscure nitrobenzaldehydes, only to return to this molecule for its robust performance and more controllable reactivity. Perfume makers also chase it for its dual-function groups, streamlining scent molecule development, thanks to the way it frees up synthetic routes that conventional benzaldehydes restrict.

    Handling, Stability, and Storage—Lessons Learned Firsthand

    Long-term partners often ask about stability—no surprise, since even tiny impurities or degradation can wreck a project. Our process minimizes moisture and oxygen intrusion; we package the material in double-lined, light-resistant containers to prevent oxidation and discoloration. One lesson our technical team learned the hard way: basic packing led to yellowing on long ocean shipments, prompting a rethink of both container lining and humidity buffer. Now, we keep each batch within acceptable color limits even after extended transit.

    Downstream, chemists regularly reach out for advice on solid handling. Our powder flows freely and doesn’t clump or cake, which matters for anyone using automated feeders or bench scoops. Overdried lots occasionally turn dusty—so our protocol brings the moisture back to a sweet spot before shipping, keeping volumetric dosing smooth and reliable. Ask anyone who’s ever dealt with a hygroscopic or sticky benzaldehyde, and they’ll share a litany of annoyances this product avoids.

    The Difference: More Than a Name

    We don’t treat all aromatic intermediates as interchangeable, and neither should formulators. The para-acetamido group in this molecule isn’t just a decorative difference on a spec sheet. Its electron-donating-nature crimps side reactions in nuanced ways that become obvious during synthesis scaleups or continuous flow runs. Years ago, we ran a head-to-head trial making Schiff bases: using ortho-analogues returned frustratingly low yields due to steric clashes. With 4-Acetamidobenzaldehyde, the reactivity opens up, enabling a cleaner product stream and fewer purification headaches.

    Comparisons often come up against unsubstituted benzaldehyde. The parent compound brings a broader reactivity, but those advantages fade if a manufacturing process hinges on selectivity or downstream protection/deprotection. In these cases, our product’s acetyl group acts both as a steering force and a temporary mask, giving chemists more control.

    Synthetic dye houses have commented on the difference in fastness and color stability depending on aromatic substitution. Many clients switched to 4-Acetamidobenzaldehyde after struggling with inconsistent supply or performance from similar-sounding compounds, reporting improvements in tone reproducibility and less batch-to-batch variability.

    Batch Consistency—A Story from the Floor

    Every manufacturer promises consistency. In reality, there’s a world of difference between buying shelf-stocked intermediates and working with material specifically made to spec for a real process. In our experience, controlling the crystallization step down to a repeatable cooling profile—one that’s been tweaked after dozens of pilot runs—saves fistfuls of time during purification and ensures bulk pharmaceutical customers don’t run into batch rejection at the final assay.

    One anecdote stands out: a client ran a multi-ton synthesis requiring the aldehyde’s formyl group to survive five processing steps that saw everything from reflux to vacuum drying. Some off-the-shelf material from a competitor fell short as the minor impurity profile dragged down the overall yield and left hard-to-remove residues. Our manufacturing team had previously narrowed the impurity window by tuning the pH at key points and reworking the washing protocol. Their project hit its targets, and years later the customer still credits material quality as a key variable in their process reliability.

    Hard Lessons in Scale: What Doesn’t Work, and What We Fixed

    Scaling up chemistry exposes every flaw. We’ve had batches go sideways due to slight lapses in temperature hold, or under-estimated stir speeds turning crystals too fine or too coarse. Learning from these mistakes, we implemented in-line particle size checks and installed improved process filters so the product meets not just purity, but also the physical characteristics our clients care about.

    Our team responds quickly to customer feedback. One pharmaceutical partner found their automated feeder jammed due to oversized agglomerates; rather than brush it off as operator error, our production manager worked side-by-side with their engineer, adjusting our drying process to deliver the right granule size. This open line, straight from shop floor to customer’s chute, made a real difference and resulted in fewer work stoppages for the end user.

    Evolving Regulatory Demands—Why Traceability Matters

    No one in regulated industries gets away with vague answers. Our manufacturing records track each lot from raw input to final output, with certificates issued by our internal QA team. Years of audits honed the paperwork and data retention process, looping lessons from even the smallest deviations back into our SOPs. For APIs and fine chemicals, trace metals testing and impurity profiling matter as much as melting point and NMR signals.

    On a personal note: sitting through a European client’s on-site audit, facing a checklist with 150+ points, brings stakes into clear focus. You don’t shortcut documentation, and consistent product identity—confirmed by newer tools like LC-MS as much as standard wet chemistry—has saved us and our clients considerable regulatory friction down the road.

    The Real-World Advantages: Less Guesswork, More Reliability

    A manufacturing operation can run only as smoothly as its feedstock allows. We aren’t just producing a molecule—we’re building a foundation for hundreds of downstream syntheses, customer projects, and industrial applications. That’s why every step, from raw reactants to final packaging, draws on direct experience troubleshooting problems that at first didn’t seem to matter, only to discover over time how small changes pay off in customer labs.

    Our technical team often consults on process tweaks. It’s not unusual for clients to call in for solvent compatibility questions, or to ask if a run can be pushed to higher throughput without sacrificing product quality. We share data across time, not just product literature, so our customers understand the real margins involved at every process stage.

    Feedback often comes in after projects finish, spotlighting what went right and which unanticipated headaches our tighter controls prevented. Our team saves these stories—they don’t make the glossy brochures, but they drive us to improve every cycle, because behind every shipment stands someone depending on it for a critical synthesis or a new invention.

    Looking Beyond Chemistry—Building Trust

    Our years manufacturing 4-Acetamidobenzaldehyde taught us technical factors will always matter, but the partnership built on trust and mutual feedback really moves the needle. Mistakes can’t be hidden, nor can successes be faked. Each production batch, big or small, comes with the experience of meeting unexpected challenges and solving them, whether through tighter impurity control, improved packaging, or reworking the entire process when it stopped meeting the mark.

    Chemists want to know their starting materials will behave, perform, and scale without troubleshooting basic chemistry. Reliable 4-Acetamidobenzaldehyde lets them focus on advancing their own discoveries instead of fighting bad ingredients. That’s what keeps us pushing process improvements and chasing better quality every cycle—because a well-made intermediate is much more than a line on a product list; it’s the backbone of innovation in hundreds of real-world labs.

    Conclusion—From Manufacturer’s Perspective to Customer’s Bench

    Stepping back, producing 4-Acetamidobenzaldehyde at scale means carrying forward hundreds of small insights earned over the years. Each modification in the process, every batch analysis, and countless conversations with customers build up knowledge not found in technical datasheets. We see our job as anticipating not just the needs of today’s chemists, but also those who invent the compounds of tomorrow. Reliable, clean, robust materials keep research moving forward and production flowing—a fact as obvious in the plant as it is on the customer’s bench. Our ongoing commitment is to deliver intermediates that help our partners get further, faster, and with less risk.