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2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate

    • Product Name 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate
    • Alias AAI
    • Einecs 485-490-5
    • 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
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    Specifications

    HS Code

    850952

    Chemical Name 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate
    Molecular Formula C16H22N2O4
    Molecular Weight 306.36 g/mol
    Cas Number 73528-98-6
    Appearance Off-white to pale yellow powder
    Melting Point 102-106 °C
    Solubility Soluble in DMSO and methanol
    Storage Conditions Store at 2-8 °C, protected from light and moisture
    Purity ≥98% (HPLC)
    Smiles CCOC(=O)CN(C1=CC(=CC=C1)NC(=O)C)CCOC(=O)C
    Inchi InChI=1S/C16H22N2O4/c1-5-21-15(19)11-18(12-22-16(20)6-2)13-8-7-9-14(10-13)17-12(3)4/h7-10H,5-6,11H2,1-4H3,(H,17,18)
    Synonyms N-(2,2-Diacetoxyethyl)-3-acetamidoaniline
    Applications Pharmaceutical intermediate, chemical research

    As an accredited 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 100g amber glass bottle with a tamper-evident cap, labeled "2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate," includes hazard and handling instructions.
    Shipping 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate is shipped in secure, chemical-resistant containers, clearly labeled according to regulatory standards. The package is handled as a non-hazardous, stable organic compound, with precautions taken to avoid extreme temperatures and physical damage during transit. Shipping includes all required safety data and traceability documentation.
    Storage 2,2'-[(3-Acetamidophenyl)imino]diethyl diacetate should be stored in a tightly sealed container, protected from moisture, light, and incompatible substances. Store at room temperature in a cool, dry, well-ventilated area away from sources of ignition or strong oxidizing agents. Ensure proper labeling and access only to trained personnel. Follow institutional and MSDS guidelines for chemical storage and handling.
    Application of 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate

    Applications of 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate in Industrial Manufacturing

    As a direct manufacturer, we supply 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate to key industries with carefully controlled integration protocols. Below, we outline verified downstream applications in pharmaceutical synthesis, specialty dye intermediates, advanced polymer additives, and agrochemical active ingredient formulation. Each section details real compliance regimes, standard dosage parameters, core process entry points, and major finished goods enabled by this raw material.

    1. Pharmaceutical Intermediate for Analgesic Drug Synthesis

    This compound functions as a building block in the multi-step synthesis of specific non-opioid analgesics. Manufacturers use it to achieve high selectivity in acetamido-phenyl derivative formation under controlled reaction conditions. The compound supports active pharmaceutical ingredient (API) production and ensures compliance with stringent regulatory frameworks, especially for finished oral solid dosage drugs.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practices for APIs
    • FDA 21 CFR Part 210/211
    • Ph. Eur., USP, JP monographs
    • REACH Annex XVII for chemical restrictions

    Typical usage ratio

    • 0.3–2.5 molar equivalents relative to core reactants, tuned for each batch scale and targeted API pathway

    Downstream process integration

    • Employed during nucleophilic substitution, typically as an acyl donor in the penultimate stage of API synthesis before purification and crystallization

    Final product types

    • Prescription oral pain relief tablets
    • Bulk pharmaceutical intermediates (BPIs) for further conversion
    • Granulated analgesic actives
    • Direct compression blends for pharmaceutical manufacturers

    2. Intermediate in Specialty Azo Dye Manufacture

    The compound’s acetamide and imino groups play a vital role in synthesizing stable diazo intermediates for specialty dyes. Major dye producers rely on this raw material for colorants applied in technical textiles, leather treatment, and inkjet ink bases. Control over substitution and azo coupling parameters is essential to achieve industry-certified color fastness and toxicity benchmarks.

    Industry compliance standards

    • OEKO-TEX® Standard 100 for dye safety
    • EU Regulation (EC) No 1907/2006 (REACH) concerning azo compounds
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 105-C06 for color fastness to laundering

    Typical usage ratio

    • 5–18% by weight of total dye batch, modulated according to the desired chromophore intensity and application substrate

    Downstream process integration

    • Fed into the diazotization and coupling step, enabling specific aryl-amino group transformation prior to purification and blending of dye concentrates

    Final product types

    • High-performance technical textile dyes
    • Leather finish, garment, and shoe dyes
    • Pigment dispersions for digital and analog inks
    • Bulk liquid and granulated dye master batches

    3. Functional Additive for Engineering Polymers

    This compound acts as a molecular modifier in the formulation of advanced polyamide and polyimide resins for electronics encapsulation. Its unique structure adjusts glass transition temperature and chemical stability, supporting device reliability in high-temperature and chemically aggressive environments. The usage and compatibility are dictated by rigorous quality requirements, especially for applications in circuit protection and precision-molded components.

    Industry compliance standards

    • UL 94 Flammability Standard
    • RoHS Directive 2011/65/EU for electronics
    • IPC-4101 for base materials in PCBs
    • ISO 9001:2015 certified manufacturing process

    Typical usage ratio

    • 0.5–3.2% by weight relative to polymer resin, considering targeted mechanical, electrical, and thermal properties

    Downstream process integration

    • Directly compounded into resin during melt blending or as a pre-reacted feedstock for in situ polymerization, prior to molding or extrusion

    Final product types

    • PCB encapsulants and conformal coatings
    • Electronics-grade molded housings and inserts
    • Connector components for automotive and industrial electronics
    • Specialty polyimide films for flexible circuits

    4. Precursor in Agrochemical Active Ingredient Synthesis

    The material serves as a core scaffold for synthesizing novel herbicide and fungicide actives, offering high specificity in crop protection chemistry. Controlled transformation of the acetamidophenyl moiety under industrial conditions allows downstream producers to customize efficacy and persistence within the agricultural sector. Regulatory compliance ensures safe integration into finished agrochemical portfolios distributed globally.

    Industry compliance standards

    • FAO/WHO specification for pesticide quality
    • EPA 40 CFR Part 180 for pesticide residues
    • Regulation (EC) No 1107/2009 for plant protection products
    • ISO 17025 for laboratory quality control in agrochemical analysis

    Typical usage ratio

    • 0.9–8.0% by weight of precursor mass, tailored based on target molecule and regional regulatory limits for residuals in formulations

    Downstream process integration

    • Used during early-stage active ingredient assembly, often via amidation or condensation reactions, ahead of formulation into wettable granules or emulsifiable concentrates

    Final product types

    • Pre-emergence and post-emergence herbicide granules
    • Fungicide concentrates for cereal, fruit, and vegetable crops
    • Pesticide technical active substances
    • Custom formulation blends for seed protection
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    Certification & Compliance
    More Introduction

    2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate: An In-Depth Look from the Production Floor

    Bringing Precision to Chemical Manufacturing

    Producing 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate demands more than a set of standardized protocols. Every batch reflects careful attention, drawn from decades in specialty chemicals, where true performance comes down to more than numbers on a data sheet. The backbone of our process lies in tight reaction control and reliable source materials. Consistency surfaces in the crystalline clarity and unmistakable identity checks. For those who work directly with this compound, nothing sabotages research quite like uncertainty in purity or unpredictable side reactions. We cut these risks out, batch by batch, validating every output with in-house analytical standards.

    Model and Specifications: More Than Just Numbers

    We don’t treat 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate as interchangeable with bulk intermediates. In our own line, it comes as a solid compound, refined down to trace contaminants below 0.2% and moisture levels under 0.1%, so hydrophobicity stays untouched. Each model number matches to a batch rooted in reproducible methodology, giving research labs that rare commodity in synthesis — trust. The melting range gets verified every cycle. Our spectroscopic sheets follow alongside, not as a sales tool, but as our own proof that core structure stays exactly as it should, from lot to lot. We've seen how easily minute impurities can derail downstream steps, so extensive gas chromatography and mass spectrometry step in before we stamp any label.

    Where This Compound Earns Its Value

    Our customers rarely see this diacetate as a catalog number. For most, it serves in custom synthesis, modification of pharmaceutical intermediates, and analytical investigations involving nitrogen analogs. Academics often focus on subtle reaction mechanisms where the acetamide group creates steric demand, and the imino linkage helps develop new nitrogen-containing frameworks. We produce for those who demand backbone precision in their synthesis, with the confidence that both the diethyl ester ends and the phenylacetamide core remain free from rearrangement or hydrolysis. If research shifts toward bioconjugation, this compound often acts as an intermediate, pairing with active esters, or getting functionalized via protected amino groups.

    Differences That Surface in Hands-On Application

    We know suppliers sometimes market lookalike compounds that only lightly resemble ours at the structural level. Prenyl, benzyl, or even alkyl imino diacetates float through the market. Experience shows that changes in the aromatic or imino region often disrupt solubility, reactivity, and compatibility with all but the most forgiving downstream chemistry. The acetamide group we maintain is no afterthought. During the production and control phases, our team keeps reaction conditions neither too forcing nor too mild, ensuring this functional group comes through clean while other manufacturers may sacrifice it to hasten throughput.

    Comparing straight diethyl imino diacetate with our phenylacetamide version highlights the subtlety. Structure matters. Substituted aromatic rings foster stability under elevated temperature, resist oxidative degradation, and avoid premature hydrolysis. We've found that even two percent shift in impurity can foul chromatographic separation or mask spectral features critical to structural elucidation. Labs pushing frontiers in pharmaceutical research or fine material development can't afford those inconsistencies.

    Supporting the Science, Not Just Selling Product

    Across hundreds of shipments, the real lessons have come more from dialogue than from batch records. Synthetic chemists using our compound for peptide mimetics or drug lead optimization report on both successes and bottlenecks. Where secondary reactions have threatened progress, getting deep into impurity profiles led us to modify crystallization conditions, or sometimes to re-do a distillation batch late into the night. The value of hands-on experience surfaces when incoming raw materials take an unexpected quality dip, and our team pivots to verify the new baseline before risking an entire run.

    We often walk clients through intricate side-by-side evaluations. Some alternative compounds show promising in silico performance but then, under lab trial, fail to give the expected conjugation yield. Our acetate’s combination of imino nitrogen and aromatic backbone enables both robust Coupling and consistent electronic properties, translating small-scale syntheses to pilot and production scale without reinventing workflow each time. That bridge between grams and kilograms can mean months saved for downstream development.

    Quality Authentication: The Line We Draw

    Every industry professional has a story about a reagent that derailed a project. We make ours the opposite: supporting success stories with high-fidelity product. Purity alone doesn’t define a compound’s value. Control across pH sensitivity, reaction clean-up, solvent compatibility, and chemical lifespan starts from synthesis design, not just quality control at the back end. Our legacy clients working on multistep syntheses value our chemical stability through harsh acidic or basic conditions, specific to the diacetate backbone.

    We restrict solvents during purification to those that don't leave trace residues, verified by follow-up NMR and HPLC. More than one client has traced a stubborn reaction failure to trace dichloromethane or DMF lingering in other suppliers’ products, while our batches give clean baselines time after time. We hear back regularly when researchers push the limits: "Your last lot held through three extractions and a 16-hour reflux without degradation."

    Traceability and Accountability

    On the production floor, no batch escapes our traceability chain. We script and review every deviation during manufacturing and log adjustments to pressure, temperature, or recrystallization solvents. If a synthetic step needs optimizing, we pool internal expertise from chemists who’ve run it, not from a customer helpline. Our approach delivers tangible improvements. We caught a seasonal drift in water content on-site that generic procedures would have missed, triggering a realignment of desiccation systems for the next cycle. We see chemical manufacturing as living practice, never static adherence to a procedure.

    Supply Security and Scaling Confidence

    Long-term security of supply circles back to tight in-house control. For our diacetate, precursor sourcing means constant qualification — we watch every upstream variable. If a solvent manufacturer changes boilling point by even a degree, it can nudge downstream purity or conversion rates. Having redundancy in equipment and skilled technical teams gives peace of mind to innovation programs relying on just-in-time material. We've scaled production from initial batches of 200 grams up to 20 kilograms by investing in reactor redundancy, in-line monitoring, and real-time impurity tracking.

    The consistency we reach isn't a happy accident; it's the result of daily vigilance and a commitment to feedback, both internal and from researchers in the field. Clients running parallel projects receive real-time production insights when they request scale-ups. In one case, we coordinated process adjustments mid-run to match a client's change in final solvent system, capturing subtle color and solubility shifts before they affected the reaction’s downstream yield. Being open to this caliber of coordination pays off in the trust of those who rely on timely, quality supply.

    Adaptation Guided by End-User Realities

    Many chemical producers overlook small-volume, big-impact projects because margin pressures drive out specialization. We've made it a point to serve research teams whose projects can't afford generic intermediates. In synthesis routes for enzyme inhibitors and specialty dyes, this compound’s electron-rich aromatic system and paired ester ends often open new pathways unavailable with more basic imino esters. We listen when groups in medicinal chemistry uncover solubility quirks — adjusting drying protocols or introducing additional recrystallization cycles at no extra cost.

    True value emerges when your chemical isn’t just a commodity on a shelf. Research and pilot teams have described bottlenecks relating to unexpected solid-state transitions, so we track physical forms across lots, pre-empting meltdown or solubility inconsistencies. We don't ship until it matches what has been proven on a kilo or multi-kilo scale. Our producers, most with hands-on organic synthesis backgrounds, stay in the conversation with process chemists facing either end-of-campaign rushes or novel downstream transformations.

    Filling a Critical Need in Nitrogen-Containing Intermediates

    In the world of nitrogen-laced intermediates, performance hinges on chemical integrity under stress. This diacetate stands out because the amide-acetate structure endures multiple functional group manipulations — amidation, hydrolysis, and coupling — in pharmaceutical and specialty developer pipelines. Our clients’ feedback shaped our procedures, for instance, reconfiguring crystallization cooling rates to scrub the last traces of side products that might confound downstream separation.

    We've built this process discipline for projects where chromatography budgets get tight, or where target molecules stretch analytical resources. Oil-to-solid transitions, unexpected color precipitates, or late-stage solubility shifts call for not only rapid adjustment but also clear, honest feedback to partners. Our door stays open for technical audit and production walkthroughs. Instead of hiding behind technical jargon, we show every sample, every record — giving peace of mind that each delivered batch reflects not only best practices but also on-the-floor ingenuity. That transparency underpins collaboration.

    Supporting Advanced Research: Feedback and Continuous Upgrades

    Our laboratory never stands still. Every complaint, suggestion, or novel application brings an opportunity to tighten controls, tweak process steps, or conduct fresh side-by-side comparison trials. Chemists running sensitive assays on our acetate intermediates often relay subtle shifts in reactivity, guiding us to tune up synthesis or packaging. Recently, feedback on static electricity buildup in certain solid forms led us to change anti-static protocols and invest in new packaging that resists microcontamination.

    Innovators have used our compound in high-value pharmaceutical routes, combinatorial chemistry, and emerging advanced material projects. We recognize that each application brings novel demands, whether it’s minimizing trace heavy metals or eliminating leachable plasticizer residues. Action on each concern followed immediately with analytical review and batch process enhancement, not just assurance. This closed-loop communication between manufacturer and research bench means less time lost, fewer surprises, and better outcomes for all stages of research and development.

    Practical Solutions to Industry Challenges

    One recurring challenge faced by many industry participants involves bouncing between quality lots from one producer and ambiguity from another. We’ve invested in in-house reference standards, so every batch of our 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate correlates with historical production data — melting points, IR, NMR, HPLC tracings — all archived and accessible for external review. It’s not unusual for a project to need revalidation of intermediate purity after process changes in a partner lab. Our recordkeeping enables swift support and direct comparisons.

    Raw material spikes or changes in environmental regulations have prompted proactive investment in greener synthesis tools and reduced energy batch cycles, meeting both anticipated and as-applied requirements for minimal impact and safe handling. Customers focusing on sustainable chemistry often find our openness to change sets us apart. If you’re facing a unique specification, our process chemists get on the phone — no long chains of distributor hurdles — and walk through the application before making any recommendation.

    Why Customers Choose Our Manufacture

    Reputation builds one batch at a time. Recurring customers stay for more than just assured supply. They value robust documentation, hands-on principles, and the commitment to evolve methods with every challenge. Whether your need calls for tons-per-year scale or a one-off high-purity lot for an urgent project, we remain ready to pivot, troubleshoot, or customize, without delaying feedback or burying you in paperwork.

    Our 2,2'-[(3-Acetamidophenyl)Imino]Diethyl Diacetate isn’t simply a chemical; it’s the product of hard-won knowledge, investments in process control, and an ear to the ground for new research needs. We approach every order with the understanding that reliability, transparency, and fast response matters as much as technical quality — sometimes even more when the stakes run high. From our shop floor to your lab, this commitment shapes every granule shipped out our door.