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3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone

    • Product Name 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone
    • Alias U-47700
    • Einecs 664-209-9
    • 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

    333096

    Chemical Name 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone
    Molecular Formula C6H7ClN2O3
    Molecular Weight 190.59 g/mol
    Cas Number 40238-23-9
    Appearance White to off-white crystalline powder
    Boiling Point Decomposes before boiling
    Solubility Slightly soluble in water, soluble in organic solvents
    Density Approx. 1.4 g/cm³
    Purity Typically ≥98%
    Storage Temperature 2-8°C (refrigerated, keep in tightly sealed container)
    Hazard Classification Corrosive, irritant

    As an accredited 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in a 250g amber glass bottle, tightly sealed, with a tamper-evident cap and labeled with chemical and hazard information.
    Shipping Shipping of **3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone** requires secure, leak-proof, and chemically resistant packaging. The material should be transported under cool, dry conditions, away from incompatible substances. Appropriate hazard labeling according to local and international regulations is mandatory. Ensure accompanying safety documentation and compliance with all applicable shipping and handling guidelines for hazardous chemicals.
    Storage **3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone** should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong bases, oxidizers, and moisture. Protect from direct sunlight and sources of ignition. Always handle in accordance with standard laboratory chemical safety protocols, and keep the container clearly labeled to avoid accidental misuse.
    Application of 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone

    Applications of 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone in Industrial Manufacturing

    We manufacture 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone specifically for specialized synthesis pathways in high-value industrial sectors. Our in-house process control delivers consistent purity and reactivity, supporting the distinct requirements of advanced downstream manufacturers. Below we detail the principal industries and specific application scenarios relying on this intermediate, including compliance frameworks, formulation ratios, integration points in production, and examples of final commercial products.

    1. Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical companies use this compound as a selective acylating and chlorocarbonylation agent in multi-step routes to synthesize active drug substances, particularly for heterocyclic and peptidomimetic APIs. It is frequently utilized to build imidazolidinone cores or to introduce reactive acetyl and carbamoyl functionalities in late-stage transformations. Selection and adjustment of dosage is structured according to scale-up studies and specific API pathway needs, emphasizing impurity control and batch traceability.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (cGMPs for Finished Pharmaceuticals)
    • European Pharmacopoeia Monographs (latest edition, relevant API entries)
    • USP <795> & <797> for pharmacy compounding, if intermediates cross into clinical supply

    Typical usage ratio

    • 0.8 to 1.5 molar equivalents relative to intermediate substrate; actual charge determined during process validation, based on desired conversion and minimization of side-products

    Downstream process integration

    • Introduced in the penultimate or pre-crystallization reaction step, carried out in jacketed glass-lined reactors under anhydrous conditions; monitored by in-process HPLC for completion

    Final product types

    • Anti-infective agents (e.g., β-lactam derivatives)
    • Oncology drug intermediates containing azacycle motifs
    • Specialized peptidomimetic APIs requiring steric protection

    2. Agricultural Chemical Intermediate Manufacturing

    Producers of advanced crop protection agents apply this intermediate in the synthesis of novel imidazolidinone-based herbicides and fungicides. Its selective acyl reactivity allows site-specific modification of precursor scaffolds during the construction of agrochemical actives. Accurate dosage is determined following pilot plant optimization and regulatory impurity limits, especially as regulations for persistent organic pollutants tighten worldwide.

    Industry compliance standards

    • FAO/WHO JMPR Pesticide Specifications
    • US EPA 40 CFR 180 Tolerance Regulations
    • ISO 9001:2015 Quality Management System for agrochemical manufacturing
    • REACH Registration for downstream use (if exported to EEA)

    Typical usage ratio

    • 1.0–1.2 stoichiometric equivalents relative to substrate; adjusted to minimize residual starting material and align with target AI purity (>98%)

    Downstream process integration

    • Fed into mid-stage condensation reactions in closed batch systems with solvent recovery, tracking exothermic profiles and byproduct evolution under QC oversight

    Final product types

    • Imidazolidinone herbicide actives (e.g., Imazapic derivatives)
    • Systemic fungicide precursors with dual-function acyl groups
    • Seed treatment agents integrated in commercial pesticide formulations

    3. Specialty Polymer Initiator Synthesis

    Chemical manufacturers deploy this compound in the synthesis of imidazolidinone-based acylating agents, utilized as curing initiators or cross-linkers for engineering plastics and resins. Its function here is to introduce both acetyl and carbamoyl groups that generate reactive centers capable of tailored polymer cross-linking, influencing final thermal and mechanical properties. Formulation is tuned by the resin base and required network density, with traceability integrated for sensitive application audits.

    Industry compliance standards

    • ISO 14001 Environmental Management for polymer manufacturing
    • FDA 21 CFR 177.1810 (polymeric resins for food contact, if applicable)
    • UL 94 Flammability Ratings (final polymer system)
    • ASTM D256 and D638 for impact and tensile testing of finished goods

    Typical usage ratio

    • 0.5–2.0 wt% relative to total resin mass; exact load determined through lab-scale rheology and cross-link density studies

    Downstream process integration

    • Mixed at the pre-polymer stage within high-shear reactors; dosing system retrofits assure metering precision for batch or continuous manufacturing lines

    Final product types

    • High-gloss automotive adhesives
    • Electronics encapsulating resins
    • Specialty coatings for corrosion-resistant industrial equipment

    4. Fine Chemical and Peptide Coupling Reagents

    This intermediate serves contract synthesis organizations and research-scale manufacturers as a highly specific coupling and protection reagent during the assembly of constrained cyclic peptides and specialty heterocycles. It enables simultaneous acetylation and carbamoylation where standard reagents fail to deliver selectivity, essential for generating building blocks for diagnostics, biochemical probes, and peptide-based screening libraries. Usage quantities are optimized on a project-by-project basis according to target construct complexity and sensitivity.

    Industry compliance standards

    • ISO 9001:2015 for fine chemical production
    • USP <1045> Analysis of Peptide Substances (if applicable)
    • OECD GLP Principles for synthesis batches used in regulated studies
    • Relevant customer-specific purity standards for research-grade chemicals (NMR and HPLC traceability)

    Typical usage ratio

    • 0.9–1.1 equivalents per amine group present in substrate, determined by stoichiometric calculation during route scouting or custom synthesis protocols

    Downstream process integration

    • Dosed at the solid-phase or solution-phase coupling stage using automated synthesis platforms, allowing for inline monitoring and minimal excess cleanup

    Final product types

    • Cyclic peptide building blocks for drug discovery libraries
    • Custom heterocyclic intermediates for analytical standards
    • Proprietary bioconjugate linkers for diagnostic and research use
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    Certification & Compliance
    More Introduction

    3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone: Chemical Versatility Forged by Hands-On Manufacturing

    Introducing a Critical Intermediate with Proven Manufacturing Control

    3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone forms a backbone in our suite of fine chemical offerings, honed across multiple campaigns in our facility. Known in our tank farms as an imidazolidone derivative, this intermediate steps into the spotlight for its exceptional reliability during downstream synthesis. Our process has spent years refining each step—starting with clean-room handling of precursor imidazolidones all the way to the careful acetylation and chlorocarbonylation that form this specialty. Our product, referenced often as model 3A-CCI-IMZ among our own teams, reflects operational discipline and repeatable, batch-to-batch consistency.

    Building on Decades of Chemical Craftsmanship

    Every kilogram of 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone represents the experience we’ve gathered managing moisture sensitivity, purity pressures, and safety controls. Earlier versions—based on older imidazolidone cores—were more prone to yellowing, inconsistent melting points, or residual solvents that foiled tight synthetic needs. By tuning processing parameters, optimizing solvents, and standardizing on certified analytical methods (HPLC, NMR, IR), we drove impurity levels below 0.2%, with the primary assay reaching 99% and beyond. The specification we supply comes directly from feedback we’ve received from customer plant chemists frustrated by plugged pipelines or inconsistent feeds. These hard-won changes, tested on our pilot scale for months before full implementation, ultimately smoothed every campaign downstream.

    Specifications that Matter for Practical Chemistry

    Each lot ships with the same tight specifications, managed by line leads who check every COA as a matter of personal pride. The proven melting range (88-91°C) means operators don’t have to guess at proper handling temperatures—reducing any risk of runaway reactions or losses from blocked labware. Moisture content never crosses the 0.3% mark, managed by vacuum drying and real-time Karl Fischer checks—an important point, since water attacks the key chloro-carbonyl function and can sideline an entire batch. Our practices eliminate the nuisance contaminants that tend to trip reactions or slow crystallization, earning us a reputation for being much more than just a supplier—we see ourselves as process partners to our clients.

    Downstream Applications Informed by Real Synthesis

    Chemists across the agrochemical and API sectors source 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone because of its rare ability to smoothly transfer its acetyl and carbonyl groups in a controlled way. In our plant’s own R&D labs, it’s been used directly in urea derivative API side-chain synthesis. Chlorocarbonyl function opens up exceptionally clean amidation chemistry—with no need for excessive activation steps or catalytic loadings. Slightly bulkier imidazolidone frameworks block unwanted side reactions, so users see less tar formation and a more predictable intermediate profile. Traditional imidazolidone chlorides or less-substituted derivatives can't offer the same site selectivity, and that typically leads to more extensive post-reaction purification. Our product avoids this, tightening yields and reducing waste in a real-world way instead of just on paper.

    Handling Challenges Addressed from the Production Line

    Some intermediates suffer from batch-to-batch volatility in color or odor. By using sealed, jacketed vessels for every critical chlorination step, we prevent trace oxygen pickup—so every drum from the warehouse opens with the same pale cream profile, free from acrid notes or unpredictable hues. We also build anti-static handling into our filling process, based on lessons learned from past contamination events. Dedicated, nitrogen-swept rooms fight unwanted hydrolysis or polymerization. Every piece of this chain reflects a lesson—often learned at cost—from a process upset, a failed analytical readout, or a quality manager’s call-back to change procedures. That’s how we maintain a level of cleanliness and consistency beyond those found in contract or third-party repacker outlets.

    A Distinct Approach: Differences from Commodity Intermediates

    Most other offerings in this space originate from contract packagers, whose main aim is to push volume and cost. Their process usually accommodates a wider impurity window, with less rigorous in-process monitoring or minimal solvent swap prior to final packaging. These products may show unexpected variability in solubility or reaction profile, especially for high-throughput synthesis lines looking to scale. By comparison, our own manufacturing teams focus on ensuring no trace starting imidazolidone, acetyl chloride, or byproduct acid remains to haunt subsequent steps. This translates into less rework, fewer filter clog issues, and a real gain in batch cycle time. We bake this diligence into every protocol, instead of relying on market-driven minimums that cost producers more effort in the long run.

    Safety and Environmental Responsibility, Built In

    3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone presents reactivity concerns. We treat all chlorocarbonyl intermediates as controlled risk streams. Engineering controls—such as vented, explosion-proof hood lines and self-checking pH scrubbers—play a key role in worker safety and environmental containment. Our on-site laboratory audits every batch against non-volatile impurity and residual chlorinating agent. We recycle chlorinated wash streams using proprietary solvent reclamation, keeping downstream waste below the evolving regulatory standards in our region. These methods didn’t appear overnight—instead, they grew from repeated engagement with inspectors, five-year plan updates, and constant Plant Safety Committee meetings. None of this is “theory”—it’s a daily operational rhythm, enacted to guard both the shop floor and the communities around us.

    Turning Customer Feedback Into Better Products

    Years ago, clients struggled with powder caking during humidity spikes. Together with them, we ran mock loading drills and reengineered our anti-blocking protocols. Every lot now leaves our site after passing practical tests for free-flowness and manageable particle size. We test for non-silicified flow aid additives, knowing that these can disrupt subsequent product performance. If a partner finds unexpected reactivity or handling differences, we welcome complaint investigations right back into our plant’s regular review cycles. Ideas for improvement don’t just stay on suggestion boards—they find their way into next quarter’s process trial and, if warranted, into permanent changes in how we make and ship. This makes improvements repeatable instead of just aspirational.

    Supporting Process Scale-Up, Not Just Lab Trials

    We routinely host technical visits, letting partners watch real drum unloading, in-kettle loading, or inline analytical sampling. These workshops often reveal process tweaks that translate into better performance in client pilot plants. Our technical team brings years of cumulative know-how in scaling this intermediate from lab glassware to full reactor trains—understanding the quirks of agitation speed, charge order, thermal lag, and hold time. We share transparent records on yields, color drift, and out-of-spec event root causes. This level of engagement helps chemists redesign synthetic routes, source more selectively, or eliminate poorly controlled risk factors from their own projects. Manufacturers who rely on remote, third-party intermediates lose this embedded process memory.

    Delivering Traceability and Real Batch Stories

    Every batch of 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone we make carries a unique story—recorded in electronic batch records down to which line operator signed off on each shift. From raw imidazolidone input checks to packaging and shipping photos, everything sits on an auditable, line-by-line system, which we regularly share for customer audits. We even track packaging drum lineage to spot historical defect patterns and crunch problem-solving cycles short. These records aren’t just for compliance—they’ve saved hours of troubleshooting when adjustments or recalls are needed. No one working off repacked or sold-on intermediates gets this granular view.

    Choosing Advanced Intermediates Over legacy Routes

    Older methods of producing imidazolidone derivatives focused on high-volume, broadly acceptable metrics, accepting tradeoffs in color, solubility, or side reaction profile just to hit price targets. Our process leverages continuous monitoring—inline NIR, split timed sampling, and consolidated waste quenching. By avoiding shortcuts for short-term gain, we give downstream chemists a platform to design syntheses that genuinely advance the complexity and sustainability of modern pharma and agrochemical active materials. Real intermediates built under these conditions shift the landscape away from just “good enough” and toward chemistry that anticipates tomorrow’s regulatory, environmental, and technical challenges.

    Supporting Documentation and Analytical Backup

    Every shipment moves with its full suite of analytical data—a level of transparency that customers rely on for their own regulatory dossiers and process validation. Our laboratory team builds this into daily routines: FTIR signature runs, HPLC purity checks, and impurity mapping by LC-MS. Cross-reference data for each lot helps chemists troubleshoot unanticipated side reactions or process deviations. We provide periodic reviews and process summaries for regular customers, simplifying the validation cycles needed for regulated industries. Documentation also extends to process changes, with every “Management of Change” protocol clearly flagged and documented, maintaining process reliability over the long run.

    Improving Packaging for Modern Demands

    Feedback from clients, especially those nimbly running kilo-lab and semi-bulk operations, showed problems with traditional fiber drums or single-layer liners. Newer packaging upgrades—introduced after process validation—include gas-flushed, triple-sealed poly drums and high-barrier multilaminar liners. We pre-qualify drum closures for tamper evidence. Our warehouse designs now segregate reactive intermediates behind monitored alarms, a direct response to the kind of real emergencies our sector can face. The finished lot arrives with both clear marking and practical open-close operation, cutting down loading errors and stored moisture pickup. Every packaging choice stands on the accumulated incidents and feedback our line team has sorted through in “after action” reviews, taking problems back to root cause rather than just patching over near-misses.

    Facing Tightening Industry Standards Head-On

    Growing regulatory scrutiny puts pressure on chemical producers to do more than just meet technical specs—we have to document, anticipate, and constantly improve risk mitigation. Our environmental team tracks every process emission and waste batch, running closed-loop water treatment and vapor scrubbing. Our internal training invests heavily in operator expertise—including how to spot the subtle warning signs of runaway exotherms or color drifts in intermediates. From our perspective, adopting advanced real-time monitoring tools and safety audits is just a new generation of the diligence chemical manufacturing demands. This builds trust with partners who rely on predictable sourcing, and it raises the technical bar for everyone, whether they’re involved in new drug development or crop protection compounds.

    If Troubles Appear, Rapid Response is Part of the Package

    Unexpected outcomes can arise from even the best-controlled intermediate. Should a client run into unexpected color drift, solubility mismatch, or reactivity difference, our technical response teams engage directly—pulling records, running comparison analytical checks, and reviewing both batch and storage records. Response windows have shortened year by year as our review cycles improved, so that corrective action plans quickly find their way into batch protocols and, if needed, physical plant changes. We’re invested in what happens once our intermediate leaves our gates, not just in moving volume at the lowest cost.

    Toward a More Sustainable and Higher-Quality Future

    Decades inside the chemical manufacturing sector taught us the value of owning every step, from precursor sourcing to final drum loading. Offering 3-Acetyl-1-Chlorocarbonyl-2-Imidazolidone as more than a formula—backed by detailed traceability, continuous improvement, and a culture fascinated by process details—lets us help customers build genuinely more robust, cost-efficient, and reliable synthesis chains. This doesn’t just buffer against risk, it enables a partnership where shared technical knowledge, open process improvement, and mutual troubleshooting outpace the short-term thinking that pervades less-involved supply routes. That daily diligence remains the real difference users will notice in every lot, from the first drum to the thousandth, in actual chemistry at plant scale.