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N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide

    • Product Name: N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide
    • Alias: Pronamide
    • Einecs: 412-010-3
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications
    HS Code 767608
    Chemical Name N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide
    Molecular Formula C13H18ClNO2
    Molecular Weight 255.74 g/mol
    Cas Number 105512-06-9
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Storage Temperature Store at 2–8°C
    Synonyms Methoxymethyl-(2,6-diethylphenyl)chloroacetamide
    Smiles CCc1cccc(CC)c1N(COC)C(=O)CCl
    Inchi InChI=1S/C13H18ClNO2/c1-4-10-7-6-8-11(5-2)12(10)15(9-17)13(16)3-14/h6-8H,4-5,9H2,1-3H3

    As an accredited N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 500g white, HDPE screw-cap bottle with tamper-evident seal, labeled with chemical name, hazard symbols, lot number, and handling instructions.
    Shipping N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide should be shipped in tightly sealed, chemical-resistant containers, protected from light and moisture. Label packages in accordance with local and international regulations. Ensure proper documentation and include safety data sheets. Handle as potentially hazardous; transport with secondary containment to prevent leaks or spills during transit.
    Storage Store **N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide** in a tightly sealed container, in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizers or acids. Protect from light, moisture, and sources of ignition. Clearly label the container, and restrict access to trained personnel. Wear appropriate personal protective equipment when handling the chemical.
    Application of N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide

    Applications of N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide in Industrial Manufacturing

    N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide is primarily pursued in highly specialized chemical synthesis fields, particularly as an intermediate in active compound preparation and specific agrochemical formulation. The following sections highlight verified industrial scenarios, compliance standards, processing integration, and practical use patterns.

    1. Agrochemical Intermediate Production for Herbicide Synthesis

    Major herbicide manufacturers utilize this compound as a functional group introducer in selective acetanilide herbicide syntheses. During production of specific chloroacetamide-based actives, its structure supports improved physicochemical profiles and process yields. R&D and commercial formulation operations require tight process controls due to its reactivity and substitution pattern. Product purity, traceability, and impurity profiling impact authorization for downstream crop protection formulations. Plants monitor storage, transfer, and inline blending to ensure batch consistency and facilitate regulatory audits."

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    2. Pharmaceutical Active Pharmaceutical Ingredient (API) Precursor Synthesis

    Pharmaceutical companies use this compound as a specialty reagent in the preparation of specific API intermediates. Its aryl and oxyalkyl groups make it suitable for use in particular analgesic or anti-inflammatory drug precursor syntheses where ortho-alkylation and amide stability are required. All processing steps demand strict segregation, solvent compatibility assessment, and documented cleaning validation to prevent cross-contamination. Operators run verification analytics on batch traceability for compliance under international GMP frameworks."

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    3. Fine Chemical Synthesis for Specialty Polymer Additives

    Chemical processors employ the material as a feedstock in niche polymer additive manufacture. Its aromatic and methoxymethyl substituents impart thermal stability and compatibility during co-polymerization and crosslinking. Used in custom synthesis for polyolefin or polyvinyl stabilizers, the material’s precise integration impacts anti-ageing properties and melt-processing uniformity. Manufacturers maintain formulation logs, conduct in-process product release checks, and retain batch samples for third-party verification under ISO quality control procedures.

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    4. Veterinary Drug Intermediate Manufacturing

    Veterinary pharmaceutical synthesis utilizes the compound for constructing side-chain protected amide scaffolds during antiparasitic active ingredient production. Facilities adopting this raw material follow stringent in-house specifications for impurity control, wall-to-wall documentation, and separation of human and animal API processing zones. Reaction conditions require precisely controlled temperature, pH adjustment, and solvent selection to sustain product equivalence and facilitate downstream scale-up to GMP-grade intermediates.

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    Free Quote

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    Certification & Compliance
    More Introduction

    N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide: Expertise from the Production Floor

    Decades in Synthesis: Our Direct Experience with Precision Chloroacetamides

    At the core of specialty chemistry, N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide stands apart for its dependable function as a tailored intermediate. We have spent years on the production line refining each batch to meet demanding downstream requirements, especially for advanced agrochemical and fine chemical formulations. Every reaction step, from raw material selection to purification, gets managed by teams in-house. This close attention reflects our belief that process controls influence everything from purity to reaction yield on the end user’s bench. Our model features a carefully monitored synthetic route, drawing on iterative improvements that emerged from both lab-scale and industrial runs. Handled correctly, each batch delivers predictable performance in synthesis work where reproducibility matters.

    Understanding What Makes This Chloroacetamide Different

    Many chemists wonder what sets this compound apart from more conventional amides or from simple chloroacetamides already in the market. The key difference comes from its distinct backbone—the 2,6-diethyl substitution on the phenyl group and the methoxymethyl moiety create selectivity and stability. In our experience, this architecture influences solubility in multicomponent reaction systems and supports clean downstream coupling. Competing amides can often introduce stray reactivities or break down more readily under process heat. Our manufacturing runs confirm the stability of this molecule, especially during multi-hour reaction processes and solvent transitions. This allows for a broader set of conditions in scale-up environments and minimizes the risk of by-product formation during key transformations.

    Consistency and Batch Uniformity: The Manufacturer’s Perspective

    One matter that seldom gets enough attention: product uniformity strongly depends on synthesis discipline. From batch to batch, trace impurities in this material can easily create downstream surprises—something most keen organic chemists have encountered with components sourced through traders or small-batch custom shops. Thanks to our internal analytics and direct process control, residual solvents and by-products stay tightly capped well below industry maximums. We employ multi-stage solvent washes, periodic vacuum distillation, and GC-MS screening at critical steps. Lab colleagues rely on this uniformity, especially in time-sensitive or regulatory-supported development timelines, and we maintain lot retention samples for traceability. Over the years, strict adherence to in-house protocols cemented trust with formulators and process chemists who require exacting specifications to replicate their results, both at pilot and full plant scale.

    Practical Applications: Downstream Value in Synthesis

    Production volumes of N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide end up primarily in intermediate steps for agrochemical active ingredient synthesis. Product managers and chemists in fungicide, herbicide, and regulated crop protection development appreciate how this molecule interacts in activated alkylations and acylations, especially with nitrogen and oxygen nucleophiles. Our in-plant pilot teams often get real-world feedback from customer R&D units about reaction endpoint stability and ease of work-up. Clients deploying this amide in heterocycle assembly, for instance, have noted improved selectivity with fewer colored by-products in their isolated yields compared to using less hindered or lower-purity alternatives. Feedback from industrial users in Asia and Europe underscores its value—the unique substitution pattern not only improves conversion rates but also preserves integrity through aggressive downstream processing with strong bases or elevated temperatures.

    Handling and Integration in Process Chemistry

    Our operators have firsthand knowledge handling this compound at plant scales, and we always insist on careful storage to preserve its activity. The crystalline solid keeps best in tightly sealed, opaque containers to avoid hydrolysis and decomposition from ambient moisture or light exposure. We prepare each lot for direct transfer to customer reactors, whether destined for multi-kilogram glassware synthesis or staged plant reactors. Dispensing teams rely on simple scoop-and-weigh protocols due to the free-flowing nature of the product; this contrasts with oily or sticky amide analogs that often gum up automated handles and require laborious manual scraping. Customers adopting rigid environmental and occupational safety standards—especially in Europe and North America—frequently mention the reduction in worker risk, since the material emits very little dust and resists atmospheric breakdown during standard bench handling.

    Technical Challenges and Solutions: What We’ve Learned in Production

    In early pilot runs, plant teams encountered solubility limits, especially in batch reactor charging with standard polar aprotic solvents. By altering crystallization techniques and introducing staged solvent back-extraction, our technical staff solved common clumping and bridging challenges. We also discovered that trace alkaline contamination in feedstocks could trigger premature side reactions, so we source only from vendors who guarantee sub-ppm metal levels—and verify with each incoming batch. This step, combined with in-house scavenger treatment, cut reaction impurity rates in half. On purity, in-process controls check for chloroacetyl and phenylamine derivatives at each stage, using both HPLC and TLC methods. As a result, customers report fewer failed scale-ups and cleaner process water. Rather than relying on one-size-fits-all solutions or vague best practices, our team put years of trial, scale, and feedback into building a protocol that keeps unwanted residues out of every drum and tote.

    Product Integrity and Regulatory Confidence

    Plant chemists working with our product routinely ask about longevity and regulatory standing, especially for applications in large-volume crop protection or fine chemical manufacture. Based on our experience, stored material remains stable over multiple years at ambient temperature in a dry, sealed space, providing plenty of shelf life for periodic campaign production. Material traceability and chemical pedigree stand at the center of not just our internal philosophy, but the formal compliance requirements of global downstream manufacturers. All outgoing shipments include detailed material identity, lot-specific purity data, and, upon request, a full history of synthetic and analytic steps. This transparency removes much of the uncertainty seen in secondary markets, where chain of custody grows opaque. Our direct-to-lab and direct-to-plant shipments also help field regulatory questions—many clients preparing commercial active substances or registering trial batches appreciate both documentation and empirical data on material quality, letting them focus on inventive chemistry rather than chasing paperwork issues.

    Differences from Standard Chloroacetamides: Lessons from the Lab and Plant

    Customers who previously worked with unsubstituted or mono-substituted chloroacetamides often comment on reaction profile differences. The dual ethyl groups at the phenyl’s ortho positions tune steric bulk, impacting how the compound participates in nucleophilic substitution and condensation. Methoxymethyl protection on the nitrogen creates a barrier to unwanted hydrolysis or over-alkylation, which tends to plague simpler amides in the same classes. Over repeated customer scale-ups, feedback has shown higher purity of target products and less time spent purifying out hydrolyzed debris and colored tars generated by over-reactive amides. Some generic chloroacetamide intermediates will react too loosely, leading to uncontrollable side product formation. In our direct plant runs, this substituted derivative upgrades operational reliability, with narrow temperature tolerance and predictable endpoint control. These attributes don’t just smooth out the main reaction—they forge a path for easier waste management and less downstream remediation, saving hours on plant cleaning and waste neutralization after cycles finish.

    Integration into Formulation Workflows

    For end users moving from lab bench to process plant, every minute saved on work-up or purification can make a tangible budget impact. Our in-house chemists provide direct process guidance, from suggestions on solvent choices to fine-tuning addition rates, because we know these parameters from our own production history. Teams seeking to optimize throughput see benefits—scope for higher loading rates, broader process windows, and a reduction in needed solvent washes. Some clients introduced our product into established protocols with only minor tweaks, noting that downstream recovery rates improved with little effort. This proves especially valuable in time-critical pilot projects or under resource pressure; companies rolling out new active ingredients for field testing do not face unexpected workflow disruptions.

    Feedback Loop from Synthesis to Scale-Up

    Direct dialogue with industrial partners brings important lessons. Our technical staff receives hands-on reports about how the chloroacetamide handled in heated reaction systems, under pressure, and under various mixing intensities. By incorporating customer observations into quality assurance cycles, we continually refine parameters like melting range, moisture tolerance, and elemental purity—not in response to hypothetical standards, but real chemical process bottlenecks. When a European agrochemical team ran into incomplete conversions using another vendor’s material, a switch to our compound yielded a measurable jump in desired product and gave their operators less time scrubbing reactors after the run. These iterative improvements result from a long-term investment in not just meeting standards, but outpacing the challenges found in real-world process environments, under the clamp of cost and compliance requirements that shape modern chemistry operations.

    Supporting Sustainable and Responsible Manufacturing

    All synthetic work produces waste, but our experience shows upstream purity and consistency dictate the total downstream environmental load. By running cleaner chemistry onsite, we minimize unreacted residues, reduce the need for excessive extractions, and keep by-product burdens in check. Sustainable solvent practices figure into both our batch planning and technical upgrade cycles; for example, we reclaimed over 80 percent of processing solvents by cycling distillation and re-using purified streams. This far exceeds the minimal requirements and shows how responsible manufacturing can meet both technical and green chemistry targets. Clients with carbon and waste reduction mandates gain measurable advantages, while plant safety officers take confidence in our adherence to data-driven emission and waste profiles.

    The Human Element: People Behind Production

    Every batch owes its quality not just to process equipment, but also to the lab and production teams behind the controls. Operators trained to spot minor irregularities act as our first line of defense, preventing small errors from snowballing into costly quality issues. Continuous training, detailed shift hand-offs, and a culture of open reporting underpin the stability of our chloroacetamide runs. This human touch cannot be separated from technical achievement. Many of our senior staff bring decades of hands-on chemistry experience, and their willingness to mentor the new generation of synthetic chemists strengthens our technical backbone. This culture of continuous improvement, coupled with internal feedback loops, means each lot gets better than the last—not because it is required, but because pride in workmanship shapes our everyday approach.

    Trust Earned Through Experience, Not Marketing

    Over the years, independent laboratory validations, customer in-plant audits, and the repeat returns from advanced synthesis teams testify to the reliability of our chloroacetamide. Unlike distributors that move containers from dock to dock, our team stays accountable for every kilo, every shipment, and every feedback cycle. Clients planning multi-year programs or working under tight regulatory scrutiny have come to count on our documented history and willingness to troubleshoot on demand. This direct accountability—born of manufacturing, not marketing—keeps attention focused on what matters: supporting innovation, protecting worker safety, and advancing chemical science by making sure the basic building blocks work as intended, every time.

    Looking Forward: Ongoing Advancements and Community Input

    The challenges of tomorrow’s synthetic chemistry will demand even more from core intermediates. By investing in new process analytics, tighter in-process controls, and close coordination with downstream partners, we aim to strengthen both the technical profile and the practical fit of N-(2,6-Diethylphenyl)-N-Methoxymethyl-Chloroacetamide. We welcome input, critical feedback, and collaborative dialog with specialty labs, scale-up teams, and formulation chemists eager to push the frontiers of what this compound can accomplish. As we move forward, our commitment remains the same: delivering not just a product, but a guarantee rooted in expertise, open communication, and respect for rigorous, fact-based manufacturing practices.

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