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HS Code |
968973 |
| Cas Number | 597-50-2 |
| Molecular Formula | C4H7NO2 |
| Molecular Weight | 101.10 g/mol |
| Iupac Name | 3-Oxobutanamide |
| Synonyms | Acetoacetamide, 3-Ketobutanamide |
| Appearance | White crystalline solid |
| Melting Point | 77-81 °C |
| Boiling Point | Decomposes |
| Solubility In Water | Freely soluble |
| Density | 1.14 g/cm³ |
| Ec Number | 209-857-4 |
| Pubchem Cid | 11828 |
As an accredited Acetoacetamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Acetoacetamide is packaged in a 500g amber glass bottle with a screw cap, featuring hazard labeling and a detailed product sticker. |
| Shipping | Acetoacetamide should be shipped in tightly sealed containers, safeguarded from moisture and strong oxidizers. During transport, it must be handled as a chemical substance, complying with local, national, and international regulations. Proper labeling, documentation, and use of appropriate hazard markings are essential to ensure safe and secure delivery. |
| Storage | Acetoacetamide should be stored in a tightly closed container in a cool, dry, well-ventilated area, away from sources of heat and ignition. Keep it separate from strong oxidizing agents, acids, and bases. Store it in a chemical storage cabinet, preferably one designed for flammable or organic compounds. Ensure proper labeling and restrict access to authorized personnel only. |
Applications of Acetoacetamide in Industrial ManufacturingAcetoacetamide functions as a critical intermediate across specific chemical industry sectors due to its unique reactivity and compatibility with specialized synthesis processes. Our manufacturing expertise ensures precise quality that meets the distinct needs of each downstream segment. 1. Pharmaceutical Intermediate SynthesisPharmaceutical manufacturers employ acetoacetamide as a building block in the synthesis of various active pharmaceutical ingredients (APIs), especially for certain pyrimidine and pyrazole derivatives. It acts as a key acylating agent during condensation reactions. The purity level, residual solvent profile, and trace metal content must align with stringent standards, as the chemical directly affects both yield and impurity profiles of targeted APIs. Its integration occurs primarily in the early-to-mid stages of multi-step organic synthesis, with quality controls extending throughout crystallization and scale-up. Industry compliance standards
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2. Agrochemical Active Ingredient ManufacturingIn crop protection synthesis, acetoacetamide serves as a primary reagent for producing selective herbicide and fungicide actives, particularly triketone or pyrazole derivative classes. Its consistent reactivity ensures predictable conversion during high-throughput batch and continuous flow synthesis lines, contributing directly to selective mode-of-action insecticides and fungicides. Downstream formulations mandate control of trace element content and batch-to-batch reproducibility, given the direct impact on crop safety and regulatory compliance for residue. Industry compliance standards
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3. Polymer Modification and Crosslinker ProductionAcetoacetamide enables production of acetoacetylated monomers used as functional crosslinkers in high-performance polymers, notably in water-borne acrylic and alkyd resin systems. The chemical's diketone structure offers enhanced cross-link density and improved bonding at the molecular level. Industrial manufacturers track residual levels and hydrolytic stability, since fluctuations affect the performance of coatings or adhesives. Materials containing acetoacetamide undergo targeted curing protocols, especially where rapid film-forming or mechanical resilience matters in the finished product. Industry compliance standards
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4. Dye and Pigment SynthesisSpecialty pigment and dye manufacturers use acetoacetamide for synthesizing acetoacetarylamide derivatives, such as monoazo pigments. Its controlled addition during diazo coupling reactions determines final pigment hue strength, dispersibility, and thermal stability. Process management focuses on minimizing batch impurity carryover and color variation, which is critical for automotive and packaging inks where performance dependability is scrutinized by downstream QC labs. Industry compliance standards
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5. Specialty Chemical Manufacturing for Chelating AgentsChemlaboratories utilize acetoacetamide as a precursor in the controlled synthesis of certain chelating agents and metal extractants. Its introduction at condensation and ring-closing stages assures selective binding characteristics for downstream applications such as water treatment, hydrometallurgy, and analytical reagent production. Quality criteria focus on residual trace impurity control and reproducibility batch to batch, driven by demand for efficient metal complexation in end-use. Industry compliance standards
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Competitive Acetoacetamide prices that fit your budget—flexible terms and customized quotes for every order.
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Many people encounter acetoacetamide just as an item in a catalogue, a chemical usually described by its formula CH3COCH2CONH2. As manufacturers, we work daily with this compound, handling it by the drum, ton, and sometimes even tanker, experiencing firsthand the properties that turn molecular potential into practical value. Whether you’re sourcing for pharmaceutical synthesis or specialty resins, you look for consistency, batch-to-batch purity, and a supplier that draws from decades in production, not just from a warehouse. We’ve produced acetoacetamide for years in a dedicated unit designed for both scale and control, drawing on controlled temperature reactions, vacuum removal of solvents, and careful crystallization to manage purity and particle size.
Over a decade ago, our chemists fine-tuned the process to get a white crystalline powder with a purity level regularly testing above 99.5% by HPLC, documented month after month. In our experience, this high assay means fewer downstream problems for our customers—clearer reactions, less filtering, lower product loss, and more reliable analytical readings during quality checks. The product’s melting point sits in the 79–83°C range, matching the expectations of users running precise heat-driven processes. Moisture is kept below 0.1%, supported by in-house Karl Fischer testing on every lot.
Downstream users often ask how impurity management sets one supplier apart from another. Trace alkali or unidentified residuals don’t just affect final product purity. In pigment manufacturing, for example, off-odors or color changes come from tiny side products in the acetoacetamide. Our team tackles this challenge through high-surface area filtration and multi-stage washing—techniques we didn’t just read about, but tweaked in response to customer feedback and recurring lab results. We keep batch records on-hand for each delivery, so tracing lines back to raw materials and process steps doesn’t stall for days.
On packaging, we’ve tried sacks, fiber drums, and lined pails, watching for caking, dust-off, or product loss during storage over humid summers. Over time, the lined fiber drum with a double seal and desiccant pouch has stood the hardest warehouse tests. Few customer complaints reach us about clumping or degraded powder, even after several months off the factory line.
Direct users have wide expectations for acetoacetamide. Some purchase it as a dye intermediate, others for pharmaceutical or agrochemical intermediates. Several large-volume customers return each year to use it for acetoacetylation reactions, where it couples with aromatic amines. They report demands for tight color and moisture limits, because yellowing during pigment synthesis can disrupt entire batches. We prepare our product accordingly, focusing as much on paleness as on dryness. Internally, our color testing routine uses the Gardner scale.
Over the years, we’ve seen demand growth in the field of polymer modification—especially as acetoacetamide acts as a latent crosslinker. Paint and coating manufacturers using our powder rely not only on consistent purity, but also on proper particle size distribution for blending. Customers facing mixing issues have told us, in clear words, where rough edges slowed their lines, and we adjusted our crystallization process in response.
Pharma customers push cleanliness, and our acetoacetamide meets their requirements not only in chemical purity, but in limits on heavy metals, which we monitor by ICP-OES with strict in-house standards. We know excipient expectations tie directly to their own regulatory obligations, and we back each shipment with certifiable data. These discussions don’t emerge in a vacuum — inspectors and formulation chemists alike drill into traceability and consistency, so our paperwork and batch samples stay available long after delivery date.
On the market, other amides like acetamide, propionamide, and even N-methylacetamide get used for overlapping functions. Some of these offer easier handling or lower cost, but none deliver both the reactive methylene group and the amide moiety in acetoacetamide’s structure. For end users running acetoacetylation or needing keto-enol tautomerism, other amides come up short or introduce extra handling steps. Acetoacetamide’s chemistry enables C-acylation and Michael reactions — routes unavailable with simple amides. Our chemists know these differences firsthand, having supported scale-ups that hit bottlenecks with alternate reagents.
During consultations with application researchers, we often hear confusion: isn’t acetamide or a diketone swap “good enough?” Not when process time or downstream crop protection regulations suspend production at the first impurity overrun. We’ve collaborated directly with scientists at coatings plants, investigating whether acetoacetamide might improve dispersibility or hardness. Comparative performance always comes down to batch analytics and the actual behavior of the compound under heat or in solution, not what a datasheet claims. Our in-house R&D continually runs these evaluations, using both legacy and new equipment, refining both the process and understanding behind our offering.
We recognize nearly every acetoacetamide buyer approaches the compound from a different technical need. Over years of direct shipments and on-site application trials, three models emerged in our production line:
Each model reflects hundreds of feedback cycles: what worked, what failed in months-long sea transport, what didn’t pass strict field tests or regulatory inspections. No solution endures unchanged — our baseline specifications shift when analytical evidence or user audits call for it.
Direct experience tells a story pamphlets can’t. In the early years, we saw caking, color shift, and the subtle changes brought by too much humidity. Many users blamed their own storage, only to find out poor inner lining or improper drying created systemic problems. We redesigned our workflows so the last drying step takes place immediately before drum filling, and monitor moisture at two separate QA stations.
In transit, acetoacetamide may spend weeks on a container ship, pass through ports with erratic warehousing, or wait in a customer’s yard for lab clearance. Each condition raises the risk of clumping or off-smells. We validate packaging by deliberately subjecting it to extended storage at elevated temperatures in our own facility, checking both color and granulation before we ever launch a new drum lining or external material. To this day, we try to preempt issues our users haven’t yet faced.
For facilities planning long-term storage, we share practical guidelines: avoid sunlight, minimize air ingress by using sealed bags within the drum, and periodically check for any sign of lumpy texture or brownish discoloration. It’s not theory — these details save batches and avoid scrap.
Being an original manufacturer, we undergo more than just annual audits. Inspection teams and client chemists may walk our production floor, review our SOPs, investigate impurity logs, or even request open access to archived batch retention samples. Our team’s knowledge doesn’t stop at compliance — it’s about transparency in every step, from solvent sourcing to documented cleanouts between grades. Auditors comment most on our raw material vetting and on the depth of our lot traceability.
Regulatory requirements continue to grow, especially for customers in Europe, the United States, and Japan. Meeting REACH or ICH guidelines on impurity profiles calls for both strong documentation and clear dialogue with users. We keep our regulatory files up-to-date, track changes in standard methods, and share all relevant test results upon request. Our chemists also revise internal processes as soon as new findings emerge from either our lab or changes in external law.
Our QA officers regularly review not just the product but also the calibration cycle of analytical equipment, cross-checking with reference standard solutions, and running duplicate tests to eliminate even low-probability misreads that could slip into a shipment’s COA.
Users shape our acetoacetamide as much as any synthetic method. A pigment manufacturer flagged a recurring faint odor, which we traced to a residual from a minor process change in our own raw supply. Our corrective action included process water replacement and a new phase in distillation; follow-up tests and direct discussions restored confidence. Another customer required a drum-by-drum guarantee on Cl content, and we added an endpoint titration step to our QA. Such demands reflect real business risks facing our partners — not theory, but missed shipments or unexpected fail grades.
Company chemists and plant managers often share their pain around downstream processing, and we’ve adapted particle size controls to address blockages in their feeding systems. Our control room logs detail every process tweak, from minor shifts in agitation speed to full overhauls of the drying phase, all born out of what our users genuinely face.
A few labs requested customized blends to match unique process parameters, and while that’s rare for acetoacetamide, we engage directly with their technical team to trial blends and get real-world feedback, incorporating those learnings back into our system.
Years in direct production taught us something few understand about acetoacetamide: supply chain stability counts as much as chemical assay. An interruption in acetylacetone or ammonia supply, regulatory surprises in import routines, or shifts in global energy pricing all land eventually on our production scheduling table. Maintaining a steady output means investing in raw material audits, secondary sourcing, and frequent realignment with transport partners to preempt bottlenecks.
R&D doesn’t pause either. As demand shifts from traditional uses towards more niche applications such as specialty hydrogels or advanced pharmaceutical intermediates, we’re developing ultra-low residue models, researching contaminant carryover from process water, and looking for eco-friendly solvent options to reduce both VOC and waste stream loads. These steps follow not just market signals but stronger calls for sustainable practice from partners who visit and audit us in person.
A challenge for all manufacturers lies in balancing cost and quality. Producing rock-solid, high-spec acetoacetamide sometimes means taking on higher inputs or longer process times, costs rarely visible outside the plant. We keep the dialogue open with our customers about what adjustments matter most and work with them to phase in upgrades that fit their needs and budget. Our operations team, chemists, and sales all spend time on customer calls to understand requirements as deeply as possible, and vet each change with in-line pilot testing before rollout across the board.
Focusing on transparency, our technical team produces white papers on process updates and shares regular summaries of long-term trends in product analytics, shipping reliability, and customer-reported impacts — not just to tick a compliance box, but to support others relying on the chemical’s performance in critical workflows.
Every kilo of acetoacetamide shipped reflects not just chemical synthesis but learning built through years of direct feedback, field visits, urgent troubleshooting calls, and determined in-house R&D. Technical dialogue with customers, open responses to regulatory and user audits, and a commitment to ongoing improvement make all the difference in what reaches your line.
By maintaining batch-level traceability, quickly addressing customer needs, and testing every process against both analytical and storage obstacles, we move beyond just making material to supporting the industries and applications that depend on its performance. Seeing our acetoacetamide’s role in your downstream compound, pigment, or formulation reminds us daily that manufacturing is more than output — it’s about understanding the reality of end use and delivering reliability, batch after batch.