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2-Chloro-N-(2,6-Dimethylphenyl)Acetamide

    • Product Name 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide
    • Alias chlorthacetamide
    • Einecs 220-650-7
    • 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

    753934

    Chemical Name 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide
    Molecular Formula C10H12ClNO
    Cas Number 709-98-8
    Appearance White to off-white crystalline powder
    Melting Point 106-110°C
    Solubility Slightly soluble in water, soluble in organic solvents
    Purity Usually ≥98%
    Synonyms 2-Chloroacetamide, N-(2,6-dimethylphenyl)-
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing The packaging contains 100 grams of 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide, sealed in an amber glass bottle with a secure screw cap.
    Shipping 2-Chloro-N-(2,6-Dimethylphenyl)acetamide is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with chemical safety regulations, using suitable materials to prevent leaks or contamination. The product requires proper labeling and documentation, with temperature-controlled or hazardous shipping procedures if applicable, ensuring safe transit in accordance with international transport guidelines.
    Storage Store 2-Chloro-N-(2,6-dimethylphenyl)acetamide in a tightly closed container in a cool, dry, and well-ventilated area away from heat sources and incompatible substances such as strong oxidizers. Keep out of direct sunlight and moisture. Label the container clearly. Use protective equipment when handling. Store at room temperature or as specified in the safety data sheet (SDS).
    Application of 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide

    Applications of 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide in Industrial Manufacturing

    As a direct manufacturer specializing in 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide, we support a range of high-value industrial supply chains with stable, scalable production. The following scenarios outline established, real-world applications where our material integrates into downstream processes under tightly controlled protocols. Each section provides in-depth detail on regulatory compliance, formulation requirements, manufacturing workflows, and end-product types recognized throughout international markets.

    1. Intermediate for Selective Herbicide Synthesis

    Within the agrochemical sector, our product serves as an essential intermediate in the synthesis of certain acetanilide-based selective herbicides, where precise substitution patterns are critical for desired selectivity and safety profiles on crop systems. Our material supports downstream processes that demand consistent purity for subsequent reactions, such as etherification or chlorination, under exacting process conditions to yield actives compliant with international agricultural use.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • Regulation (EC) No 1107/2009 concerning plant protection products (EU)
    • EPA 40 CFR Part 180—Tolerances and Exemptions for Pesticide Chemicals in Food (USA)
    • ISO 17034 Reference Substance Production

    Typical usage ratio

    • Used at 1–7% by mass of total batch composition for target molecule synthesis; actual charge depends on downstream methylation or chloro-substitution step yields and desired throughput.

    Downstream process integration

    • Charged to the reactor in the initial coupling or N-acylation steps, often dissolved in organic solvents (e.g., toluene, acetone) with controlled temperature profiles; further transformed prior to formulation of finished herbicide EC, SC, or WG products.

    Final product types

    • Selective herbicidal actives (e.g., chloroacetanilide herbicides)
    • Formulated agricultural suspension concentrates (SC)
    • Emulsifiable concentrates (EC)
    • Water-dispersible granules (WG) for crop protection

    2. Pharmaceutical Intermediate for Analgesic APIs

    In regulated pharma manufacturing, this compound enters as a building block for select non-opioid analgesics in the anilide class, where its reactivity profile and substitution pattern define biological activity. Pharma sites introduce it under GMP-controlled environments, leveraging its purity in amidation or condensation reactions with tight QC on metal and impurity residues to meet pharmacopeial standards for subsequent API conversion.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopeia (Ph. Eur.) and United States Pharmacopeia (USP) reference monographs
    • Drug Master File (DMF) registration (FDA/EMA as applicable)
    • 21 CFR 210/211 Current Good Manufacturing Practice (cGMP)

    Typical usage ratio

    • 0.8–1.5 molar equivalents per batch, adjusted according to the stoichiometry of the target API’s core structure and process yield requirements.

    Downstream process integration

    • Fed into an amidation or acylation reaction during stage II or III of multi-step synthesis, typically after initial aniline functionalization; monitored for conversion and residuals before direct transformation into final API followed by purification and crystallization.

    Final product types

    • Anilide-derived analgesic active pharmaceutical ingredients (APIs)
    • Bulk pharmaceutical intermediates
    • Tablets and oral dose formulations (after API integration)
    • Pharmaceutical reference standards

    3. Precursor for Specialty Dye Manufacturing

    Textile and specialty dye producers incorporate our compound as a key aromatic amide for synthesizing high-performance dyestuffs, particularly where shade fastness and resistance to chemical laundering are paramount. Our product’s substituted phenyl backbone impacts chromophore formation in azo or anthraquinone dye synthesis, dictating the stability and shade profile of textile colorants.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for textile raw materials
    • REACH Regulation (EC) No 1907/2006 Annex XVII (Europe)
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 9001:2015 Quality Management for Dye Manufacturing

    Typical usage ratio

    • Varies from 2–12% by mass in precursor charge for dye intermediate synthesis depending on the target dye type and reaction pathway selectivity.

    Downstream process integration

    • Introduced during nucleophilic substitution or coupling stages, often in batch reactors under controlled pH and temperature to maximize chromophore yield; followed by diazotization, coupling, or sulfonation as per the dye’s structural design.

    Final product types

    • Substituted azo dyes for synthetic textiles
    • Anthraquinone dyes for high-sunlight exposure fabrics
    • Reactive dye intermediates for cellulosic fibers
    • High-stability pigment dispersions

    4. Synthesis of Fine Chemical Additives for Polymer Modification

    Polymer additive manufacturers use our acetamide compound as a precursor for functional additives that fine-tune the compatibility, viscosity, and thermal performance of engineering plastics. The substituted amide motif lends itself to downstream nucleophilic or condensation reactions, introducing unique chemical resistance or flow-control characteristics to thermoplastic and thermoset end products.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical modification processes
    • USP Class VI biological reactivity testing (for plastics in pharmaceutical use)
    • 21 CFR §177 (FDA regulations on indirect food additives for polymers)
    • RoHS Directive 2011/65/EU (for electronic plastic components)

    Typical usage ratio

    • Typically blended at 0.3–5% by polymer mass; formulation adjusted based on polymer matrix (polyolefin, PVC, engineering resins), desired additive loading, and performance characteristics.

    Downstream process integration

    • Charged during pre-polymerization stages or introduced as a masterbatch additive during melt blending; undergoes in situ functionalization or reacts with existing polymer chains to yield enhanced final performance during extrusion or injection molding.

    Final product types

    • Antistatic and processing aids for injection-molded plastics
    • Heat-resistant polymer modifiers
    • Film-forming additives for food packaging
    • Polymer dispersants for masterbatch production
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    Certification & Compliance
    More Introduction

    2-Chloro-N-(2,6-Dimethylphenyl)Acetamide: Purpose-Driven Chemistry

    Crafting Value in Modern Chemistry

    Manufacturing 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide stems from a clear need in chemical synthesis: dependable, well-defined intermediates. We focus on this compound not as a mere product but as a purposeful building block. Over years in the business, the influence of quality and traceability stays constant, especially when the final uses involve agrochemicals, pharmaceutical intermediates, and specialty organic syntheses.

    We embrace the hands-on realities of the lab and the plant floor. Our 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide, often recognized in the industry as CDA, stands up to scrutiny because its profile—physical, chemical, and impurity spectrum—reflects methodical control. Material that isn’t monitored right from the charge of raw starting materials to the detailed filtration and packaging steps rarely passes muster here.

    Defining Purity Through the Manufacturing Process

    Our team starts with the selection of 2,6-dimethylaniline and monochloroacetic acid, avoiding unreacted amines that can darken the finished acetamide or complicate downstream chemistry. Tracked batch records reveal years of optimization: we favor chlorination with minimal by-product formation, and we put real work into refining the work-up to prevent residual salts and colored impurities. Completion is never called until purity is validated on each lot. We don’t send out a batch unless the key parameters meet a strict HPLC threshold, and melting point confirms identity within an established, repeatable range.

    The benefits come into focus with fewer side reactions, less wasted solvent in cleanups, and more reproducible results for our partners in pharmaceutical research. From our lab notebooks, we know trace impurities, often thought ignorable by some, actually shadow the outcome of later synthesis steps—either by poisoning catalysts, blocking transformations, or simply by spreading uncertainty through a process chain. We invest in longer vacuum drying and double-check with independent NMR verification, not only because it’s the right thing to do but also because we see time and again that cost savings down the line outweigh savings at the production stage.

    Consistent Chemical Identity, Consistent Results

    What matters most to us is reliability. CDA, like many acetamides, has a solid crystalline form and melts sharply. What varies from one supplier to another—and gives ours a practical edge—is how consistently these properties show up from batch to batch. Formulators report back that their procedures stay on track only when physical consistency holds; clumping, off-color, or variable particle size can spell downtime or noisy results. We mill and sieve on-site, so our product flows and disperses smoothly, reducing handling losses.

    Moisture content challenges every batch—hygroscopic powders pick it up fast if left exposed. We never underestimate the risk of small moisture spikes. Too much, and storage stability, reactivity, or even shelf-life can collapse. Every time we rotate drums in our warehouse, we check seals and monitor desiccant levels, tightening up protocols to keep every shipment within spec.

    Roles in Downstream Chemistry

    2-Chloro-N-(2,6-Dimethylphenyl)Acetamide holds a respected role as an intermediate for certain herbicide chemistries. From our workshop benches to kilo labs of our global partners, CDA serves as a point of access for various substituted amide derivatives. One common application comes in the synthesis of acetanilide herbicides—where purity influences selectivity and safety of the end-use product.

    Many pharmaceutical projects rely on its reactivity: the strategic chloro group makes it a preferred candidate for SN2 substitutions, nucleophilic aromatic substitutions, and custom acylations. Unlike structurally similar acetanilides without the ortho methyl groups, our acetamide’s increased bulk at the phenyl ring can slow down undesired side reactions. Chemists working on complex molecules often come back for this selectivity—they can pilot new routes to active pharmaceutical ingredients without constant troubleshooting.

    We’ve had process chemists visit our site, even bring their own analytical tools, keen to see for themselves how our batches compare under their protocols. Their feedback shapes our own QC pipeline: years back, a customer flagged unexpected residues in a downstream methylation; collaborative root cause analysis pinned it on a contaminant in a previous run. We honed in on temperature control in the chlorination stage, and since then, neither we nor our clients have run into that snag again.

    Separation from Other Intermediates

    Many in the business ask what sets this compound apart from the flood of generic acetanilides. The answer ties back to structure and function. Not all aromatic acetamides deliver the same performance in synthetic pathways; the two methyl groups flanking the amino function in 2,6-dimethylaniline give downstream products unique steric properties. They can alter the biological profile and selectivity in pesticide and pharma targets. Parallel experiments—comparing CDA with, say, 2-chloroacetanilide or its monomethyl analog—often result in noticeable differences in reaction rates and impurity patterns.

    Buyers familiar with laborious purification steps appreciate that our CDA avoids the “sticky byproduct” phenomenon documented with higher levels of ortho-substitution or poorly washed post-reaction material. Real-world cost savings arise at the user end: less time spent dealing with post-synthesis clean-up or re-crystallizations, fewer losses, and, crucially, more reliable analytical results.

    Analytical Data: What Quality Looks Like

    We provide analytical reports that matter to chemists—no generic check-box lists. Melting point runs within a degree of literature values. IR scans reveal the expected amide carbonyl stretch, giving confidence in identity before further work. We set GC and HPLC thresholds not just for major contaminants but for minor byproducts from incomplete chlorination or side-ring alkylations. Transparency in data isn’t just a slogan: we attach spectral records for each batch, knowing that our customers’ trust rides on reproducible evidence.

    Loss on drying remains one of the easiest yet most meaningful checks. A well-dried sample tells a story about diligence during processing. From direct conversations with end-users, we know how minor shifts in water or solvent content—remaining from poor vacuum finish—can handicap downstream synthesis. So we extend vacuum drying cycles even at a small cost to our own throughput, favoring better results for the customer over simply maximizing output.

    Stability and Storage: Lessons from the Warehouse

    Experience has shown that packaging acetanilides without due care can spoil half a year’s worth of effort in a matter of weeks. Early years taught us this lesson: moisture picked up in damp or sub-standard packaging can alter both handling and chemical properties. Every batch gets packed in lined, airtight containers, double checked for seal integrity. We’ve introduced nitrogen blanketing for export shipments, based on direct evidence that transport in humid conditions can trigger unwelcome hydrolysis and spoil end-use applications.

    Stability checks extend past the regulatory minimums—accelerated aging, photostability, and real-time monitoring. It’s not enough to stamp an expiration date: we need to know the material acts as expected after weeks in a warehouse or months at sea. Selection of appropriate drum liners and secondary containment doesn’t result from guesswork but from repeated feedback from customers in diverse climates.

    Supporting Sustainable Practices

    We face pressure to both improve efficiency and reduce waste. Chemicals like this acetamide require drive toward cleaner processes, lower emissions, and safe handling. We reclaim solvents where practical and neutralize byproducts before disposal. Our own team tracks developments in green chemistry—each incremental improvement in the synthetic route, such as selective addition or better filtration, finds its way into scaled production only after pilot confirmation that yields and purity hold up.

    A sticking point in the industry: some routes use excessive chlorinated solvents or unrecoverable mineral acids. We invest time in improving work-ups, aiming for a process that handles effluent responsibly, not just to satisfy regulators but out of professional pride. We keep an eye on solvent and energy use per tonne of product, striving to beat last year’s records, knowing full well that sustainable practices strengthen both our bottom line and the reputation of the sector.

    Regulatory Alignment and Traceability

    Chemical manufacture walks in lockstep with regulatory frameworks. Customers expect clean, compliant product—and regulators demand process transparency. Traceable batches matter, from source materials through to final drums. We log every batch in digital records, making recall or investigation possible long after shipment. Audits, both internal and third-party, play a role not only in keeping us accountable but in spotlighting new routes for improvement.

    We’ve witnessed how weak recordkeeping leads to product recalls or delayed submissions in pharma and agro projects. Not a risk we’re willing to accept. So the batch records stay detailed and audit trails trace the journey of each drum, down to raw material certificates and in-process checks.

    Research Partnerships: Sharing Risk, Boosting Results

    Our history includes direct collaborations with university labs and industrial R&D centers. These relationships go both ways: groups trial our 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide for exploratory syntheses, and we field regular calls about reactivity, incompatibilities, or solvent pairings. Sometimes, new side products or application feedback spurs a joint lab inquiry, with process improvements following successful trials.

    For graduate students navigating complex synthesis, access to well-defined intermediates like CDA can make or break a project’s timeline. We offer mentorship, supplying not just product but process discussions. More than once, a tricky bottle neck in their sequence resolved with a shift in product grade or a fine-tuned re-crystallization protocol we developed in house.

    As the landscape of chemical manufacturing evolves, dialogue between bench chemist and plant operator matters more than ever. We encourage open communication, quick feedback cycles, and data transparency. Some process engineers have shared unpublished improvements after working with our compound—those details shape next-generation protocols and yield stronger products, tighter tolerances, and more efficient syntheses.

    Choosing the Right Acetamide Makes a Difference

    Over the years, we’ve learned that a choice of intermediate often defines a project’s destiny. Users who pivoted away from generic or poorly characterized sources have seen gains in both project speed and reliability. Stories from downstream—delays caused by mystery impurities, sluggish reactions, or inconsistent crystallizations—remind us daily that investment in robust materials pays for itself.

    Chemists need intermediates that arrive as expected, weigh out smoothly, and require no frantic troubleshooting. Our objective remains clear: ship a 2-Chloro-N-(2,6-Dimethylphenyl)Acetamide that meets analytical standards and practical needs, backed by real-world experience and continuous process improvement.

    The Road Ahead: Meeting Today’s and Tomorrow’s Needs

    With rising regulatory demands, rapid development timelines, and the continuing shift toward more sustainable chemistry, intermediates like this stand at a crossroads. Routine approaches won’t suffice. Iterative process upgrades, real communication with users, and relentless attention to batch-to-batch consistency anchor our agenda. We see our role not just as producers, but as facilitators for innovation, responsible sourcing, and long-term partnerships.

    From small test batches for pilot studies to full-scale runs supporting launches, our guiding principle endures: let the compound work for the chemist, not the other way around. We never stop questioning, probing, and refining our craft, knowing every gram we ship finds purpose in the hands of people who shape tomorrow’s breakthroughs.