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4-Acetylamino-2-(Diallylamino)Anisole

    • Product Name 4-Acetylamino-2-(Diallylamino)Anisole
    • Alias 4-AADA
    • Einecs 629-022-2
    • 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

    353446

    Chemical Name 4-Acetylamino-2-(Diallylamino)Anisole
    Molecular Formula C15H20N2O2
    Molecular Weight 260.33 g/mol
    Cas Number 139042-22-3
    Appearance Light yellow solid
    Melting Point 96-98°C
    Solubility Soluble in organic solvents
    Storage Conditions Store at 2-8°C, protected from light
    Purity Typically ≥98%
    Synonyms 2-(Diallylamino)-4-(acetylamino)anisole
    Smiles COc1cc(N(C=C)C=C)ccc1NC(C)=O

    As an accredited 4-Acetylamino-2-(Diallylamino)Anisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Sealed amber glass bottle containing 25 grams of 4-Acetylamino-2-(Diallylamino)Anisole, labeled with safety information and lot number.
    Shipping 4-Acetylamino-2-(Diallylamino)Anisole is shipped in compliance with chemical safety regulations. It is securely packaged in sealed containers to prevent leakage or contamination and labeled according to relevant hazard guidelines. Shipping typically requires appropriate documentation and may necessitate temperature control and/or hazardous materials handling, depending on regional transportation requirements and the compound’s classification.
    Storage Store 4-Acetylamino-2-(Diallylamino)anisole in a tightly sealed container in a cool, dry, well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect from light, humidity, and sources of ignition. Clearly label the container and ensure it is placed in a dedicated chemical storage cabinet. Use personal protective equipment when handling to avoid exposure.
    Application of 4-Acetylamino-2-(Diallylamino)Anisole

    Applications of 4-Acetylamino-2-(Diallylamino)Anisole in Industrial Manufacturing

    4-Acetylamino-2-(Diallylamino)Anisole is a specialized intermediate used in advanced fine chemical production. We manufacture this material for customers demanding consistent quality and tailored physical properties. Below, we outline its application in core downstream industrial sectors, focusing on true-to-market use cases and practical production integration.

    1. High-Performance Polymer Additive for Conductive Plastics

    This material serves as a reactive monomer or functional amine component in the synthesis of conductive polymers. It is often used in electronics grade plastics where antistatic or conductive properties are essential. Our clients integrate the compound via controlled copolymerization or grafting techniques, benefiting from its diallyl and acetylamino groups, which enable crosslinking and improved dispersion. Process engineers adjust blend ratios based on target electrical resistance and mechanical flexibility.

    Industry compliance standards

    • IEC 61340 (Electrostatics – Standard for conductive and antistatic materials)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 9001:2015 (Quality Management in Manufacturing)
    • REACH Regulation (EC 1907/2006) substance registration and usage review

    Typical usage ratio

    • 0.2%–3% by weight, adjusted for target conductivity and compatibility with base resin

    Downstream process integration

    • Added during resin blending or masterbatch compounding prior to extrusion or injection molding

    Final product types

    • Antistatic device housings for consumer electronics
    • Conductive polymer films for flexible printed circuits
    • Automotive electronic component casings
    • Plastic trays for ESD-sensitive semiconductor transport

    2. Intermediate for Reactive Dyestuff Synthesis

    Our material features electron-donating and crosslink-ready functionalities, making it a key intermediate in the chemical synthesis of reactive dyes. These dyes target cellulose fibers for deep color penetration and washfastness. The compound supports coupling reactions and stabilizes chromophores during dye finishing steps, allowing formulators to achieve highly specific color shades meeting apparel and textile market needs.

    Industry compliance standards

    • OEKO-TEX Standard 100 Annex 4 (Textile Chemical Inputs)
    • ZDHC MRSL 3.1 (Zero Discharge of Hazardous Chemicals)
    • ISO 14001 (Environmental Management in Dye Manufacturing)
    • GOTS (Global Organic Textile Standard) for input chemistry

    Typical usage ratio

    • 5%–18% of total synthetic dye molecule weight, fine-tuned for desired hue intensity and reactivity

    Downstream process integration

    • Incorporated during multi-step azo or anthraquinone dye synthesis before final purification and granulation

    Final product types

    • Reactive dye powders for industrial textile dyeing
    • Liquid dye concentrates for commercial fabric printing
    • Eco-compliant dyes for children’s apparel
    • Specialty coloration products for sportswear

    3. Precursor in Active Pharmaceutical Ingredient (API) Synthesis

    The molecular structure of this compound supports its use as a building block in the preparation of APIs requiring dual amine and acetyl functionalities. Medicinal chemists use it in the assembly of molecules where controlled functional group orientation is imperative, such as select antihistamine agents and experimental small-molecule drugs. Batch record control ensures traceability and consistent purity in regulated environments.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Inactive and Active Pharmaceutical Ingredients)
    • USP–NF (U.S. Pharmacopeia–National Formulary) specification for starting materials
    • EDQM CEP (Certification of Suitability)
    • 21 CFR Part 211 (FDA cGMP for Finished Pharmaceuticals)

    Typical usage ratio

    • Batch-specific; stoichiometrically determined per target API structure and synthesis route; generally 1–1.5 molar equivalence in primary coupling reactions

    Downstream process integration

    • Introduced during the intermediate or penultimate coupling stage of multistep chemical synthesis workflows under cGMP conditions

    Final product types

    • Pharmaceutical intermediates for antihistamine development
    • Precursors for experimental oncology medications
    • API building blocks for contract manufacturing organizations
    • Specialty ingredients for niche small-molecule drugs

    4. Ingredient for UV-Absorbing Coating Formulations

    The aromatic and amine functionalities of our product enable its integration into advanced UV-absorbing polymers and coatings. Industrial formulators use the compound as a UV filter precursor or as a co-monomer for crosslinkable ultraviolet-blocking systems. Its addition helps to enhance outdoor durability in architectural and automotive surface treatments. QC protocols monitor the photostability imparted by its incorporation at different film thicknesses.

    Industry compliance standards

    • ISO 16474-2 (Artificial Weathering of Coatings – Xenon-Arc Exposure)
    • European Paint Directive 2004/42/EC
    • GB/T 9754 (Chinese National Standard for Paints and Varnishes: Gloss Measurement)
    • ASTM D4587 (Fluorescent UV Exposure of Plastic Panels)

    Typical usage ratio

    • 0.5%–4% by polymer mass, depending on exposure requirements and base resin UV susceptibility; formulation trials determine optimal levels

    Downstream process integration

    • Dispersed in prepolymer resin pre-mix or introduced during in situ polymerization, sometimes postaddition before final cure

    Final product types

    • UV-resistant architectural paints
    • Automobile clearcoats for exterior protection
    • Plastic substrates for outdoor displays
    • Protective films for solar panels

    5. Crosslinking Agent for Advanced Epoxy Resins

    This specialty chemical acts as a curative or co-curing agent in the formulation of high-performance epoxy resins. The presence of diallylamino groups supports crosslink reactions for thermoset composites. Manufacturers select this material to achieve specific glass transition temperatures and chemical resistances in heavy-duty applications, including aerospace and electronic encapsulation. Process engineering teams calibrate dosing to maintain balance between hardness and flexibility.

    Industry compliance standards

    • UL 94 (Safety for Flammability of Plastic Materials)
    • IPC-4101 (Specification for Base Materials for Rigid and Multilayer Printed Boards)
    • EN 45545-2 (Fire Test for Railway Components)
    • ISO 9001 (Resin Manufacturing Quality Systems)

    Typical usage ratio

    • 1%–6% by weight, operator-selected based on desired crosslink density and end-use temperature performance

    Downstream process integration

    • Mixed with epoxy pre-polymers during resin batching or added as secondary curative during part molding or lamination

    Final product types

    • PCB base laminates for electronics
    • Structural adhesives for transportation
    • Casting resins for electrical insulators
    • Composites for aircraft interiors

    6. Modifier in Specialty Lubricant Additive Packages

    We supply this compound as a functional additive component in the development of advanced lubricant formulations, particularly where high-temperature and oxidation resistance are required. The nitrogen and ether functionalities provide potential antioxidant and antiwear properties, improving performance in energy sector and industrial gear lubricants. Formulators run compatibility and performance tests to set concentration, ensuring full compliance with heavy machinery service standards.

    Industry compliance standards

    • ASTM D4951 (Standard Test Method for Additive Elements in Lubricating Oils)
    • API Service Categories (American Petroleum Institute Lubricant Classifications)
    • DIN 51517 (German Standard for Industrial Lubrication Oils)
    • ISO 21469 (Hygiene Requirements for the Manufacture of Lubricants)

    Typical usage ratio

    • 0.1%–0.8% in finished lubricant blends, depending on interaction with base stocks and target application stress loads

    Downstream process integration

    • Introduced into additive package concentrates before blending with base oils in final lubricant mixing operations

    Final product types

    • Synthetic gear oil for wind turbine gearboxes
    • High-performance compressor oils
    • Industrial hydraulic fluids
    • Specialty greases for steel plant equipment
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    More Introduction

    4-Acetylamino-2-(Diallylamino)Anisole: Direct from Our Factory

    An Introduction Based on Chemical Experience

    At our manufacturing site, we have engaged with specialty aromatic amines for decades, and in that time, we have seen how subtle changes in molecular structure can make all the difference in the lab and on the plant floor. Among the compounds earning renewed attention for their performance in both research and industry is 4-Acetylamino-2-(Diallylamino)Anisole. Our production team knows this molecule well, both in handling at scale and in seeing where it succeeds over similar chemicals.

    Understanding the Product: Model and Character

    We synthesize 4-Acetylamino-2-(Diallylamino)Anisole with a focus on robust purity, reliable repeatability, and well-controlled batch traceability. Colleagues in pigment synthesis, custom dyes, and pharmaceutical intermediates have come to us specifically for this product. The powder, usually white to light yellow, releases a mild aromatic odor. We keep moisture and ash to tight minimums with every batch, since trace impurities can derail a critical downstream reaction.

    Our controlled synthesis route produces this compound with a purity above 99 percent by HPLC, ensuring suitability for research and industrial use. Typical molecular formula is C15H20N2O2, with a molecular weight of around 260.34 g/mol. Such direct information helps our partners avoid calculation missteps. We provide both technical and advanced-grade specifications, responding to different tolerance thresholds required by various customers involved in electronics, pigment, or fine chemical work.

    Where We Have Seen 4-Acetylamino-2-(Diallylamino)Anisole Used

    The true value of any material comes to light when used and tested across multiple fields. Our staff have watched the product become an important intermediate in the development of azo, anthraquinone-based, and extended conjugated organic dyes. The diallylamino group means this molecule reacts well in further alkylation steps, while the anisole ring supports electron density needed for color development or targeted pharmaceutical mechanisms.

    We often see this compound used as a critical building block in:

    As chemical manufacturers, we supply not just material but insight. Our technical team has helped partners increase reaction yields in amination, reduce side products during N-alkylations, and troubleshoot recalcitrant product purifications by supplying solvent residue data and stability profiles on our 4-Acetylamino-2-(Diallylamino)Anisole. Feedback from customers developing new high-performance dyes for industrial ink-jet printing has let us refine our quality to suit real market needs.

    What Sets Our Process and Product Apart

    Every chemical has its fingerprints. We produce 4-Acetylamino-2-(Diallylamino)Anisole with a direct understanding of trace contaminants encountered in large-scale reactions. Our process avoids raw material streams that lead to halogen, sulfur, or nitro-group residues, so downstream reactions run clean. This becomes especially important for users seeking to minimize purification burdens in later stages.

    Unlike basic methylated anilines or simple dialkylamino anisoles, the diallyl chain in this molecule creates unique reactivity. Extended π-conjugation boosts optical properties for dye chemists and improves solubility in organic media. For drug development groups, this same functionalization means they can more easily introduce further functional groups via cross-coupling or cyclization.

    Other manufacturers sometimes leave behind polymerizable impurities or variations in functional group content, especially when running older, batch-based routes. We run continuous-flow purification across inert atmospheres. This keeps peroxide levels and oxidation below thresholds for high-value pharmaceutical or dye reactions, based on the feedback we have received. Every batch comes with fresh spectral and chromatographic data collected and available, traced back to the original feedstock.

    Lessons from Manufacturing Scale-Up

    Having worked on both kilogram and multi-ton lots, we learned that certain properties must be maintained at every scale. Small amounts of residual water or byproducts might escape detection at lab scale but can cause polymerization, gelling, or discoloration in plant-scale work. We introduced extra gas-stripping at final purification, dried under low pressure, and store the product under nitrogen so no off-smell or off-color develops.

    We track trends in product physical properties, recording fine shifts in melting point, bulk density, or flowability that could indicate subtle variations in batch processing conditions. This data has helped not only our team but also customers working on larger synthesis campaigns. It allows us to troubleshoot if a partner calls with an unexpected drop in purity or a color body issue, drawing from our years of direct experience.

    One area where our compound outperforms simple analogues is in lower tendency to absorb moisture from air. Storage and shipping thus become less fraught with risk. In repeated warehouse audits, we've measured stability over periods up to a year, with very little caking, no detectable loss in HPLC purity, and consistent performance in end-user reactions. For many intermediates, this level of confidence means fewer last-minute process changes at the factory.

    Clearing Up Common Confusions

    The specialty nature of 4-Acetylamino-2-(Diallylamino)Anisole means it sometimes gets confused with similar-sounding amino-anisole derivatives. The difference lies in both the minor group shifts and in handling at scale. Customers have contacted us after using analogues (like diethylamino instead of diallylamino) that led to inconsistent color, batch-to-batch yield swings, and processing surprises. The optimized reactivity of our product—thanks to its structure—reduces these headaches.

    Another frequent issue comes with competing materials sourced from outside the original manufacturer. Traders and third-parties often offer similar compounds without tight control on quality tracing. Knowing the identities and origin of every raw material allows our customers to satisfy their internal auditing teams and external regulators, and provides assurance that future regulatory documentation will not fall short.

    Practical Considerations: Packaging, Storage, and Transport

    Direct experience taught us that packaging has as much impact on product usability as technical grade. We use anti-static, high-barrier polyethylene drums to prevent any contamination or degradation over time. In regions with sensitive humidity or for customers working in hot climates, we add desiccant packs and run in-line moisture checks prior to dispatch. Our inventory team logs each drum's weight at shipment and after transport, helping to spot any transport shocks or breaches.

    The product’s physical solid nature lends itself well to both large-batch dispensing and re-sealable storage in smaller amounts for R&D setups. Colleagues in ink and pigment industries who work with pre-measured portions have reported little dust or scatter during dispensing, thanks in part to our attention to powder handling and fill control. In our experience, these details limit product loss and cleaning chores.

    Comparing Functional Differences: Technical Distinctions That Matter

    Chemists know that group placement on the aromatic ring and overall molecular symmetry influence not just reactivity but also solubility, color, and physical stability. The acetylamino group at position 4 increases thermal resistance and restricts unwanted side reactions, which has shown clear improvements over simple 2,4-diamino anisole in dye and polymer research. Meanwhile, the 2-position diallylamino opens up extra reactivity vs. dialkylamino analogues, providing more flexibility in building more elaborate molecules.

    Our team worked with several academic labs experimenting with new photoresists; they reported much higher yield and clarity in their photochemical coatings, tied directly to the reduced impurity levels and optimized functionalization from our production route. This stands in marked contrast to competitors’ versions that frequently led to inconsistent film formation or necessitated additional pre-treatment steps.

    Pharmaceutical researchers have especially valued the defined acetyl group, which in metabolic simulations appears to grant improved stability compared to unprotected amines, reducing off-target metabolic oxidation. We have had formulation teams in international pharma partner with us repeatedly because our grade avoids catalyst poisons—subtle elements like iron or copper—that can sabotage kilogram-scale couplings. By avoiding legacy glassware and sticking to modern, lined reactors, we keep contamination out where it counts most.

    Supporting Innovation in Application

    Over the years, we have seen how the right intermediate, at the right grade, sparks progress. Advanced pigment and electronic ink researchers have looked to our 4-Acetylamino-2-(Diallylamino)Anisole for its consistent performance in both lab trials and full-scale manufacturing. Consistent color strength in the end product has made it a regular call-in supply for pigment companies working with custom shades and permanent colorants. This reliability supports their exploration of new functional pigments without risking rework or failed production batches.

    The pharmaceutical field is especially demanding of trace-level purity. Teams screening new compounds for CNS-active drugs, where minor nitrogen-based impurities can skew data, have commented positively on spectra comparisons from our supplied lots. Their teams have cited less “background noise” in NMR and LC-MS, translating to cleaner reaction profiles and sharper analytic endpoints.

    A number of our dye-manufacturing partners notice improved rate of coupling and color fixation, with minimal formation of side products or problematic isomers. This performance, we have learned, comes from tight structure control and uniformity of the diallylamino and acetylamino substituent placement—a mark of our synthetic sequence. Other manufacturers sometimes neglect these details, leading to laborious downstream separations and disappointing yield.

    Troubleshooting and Feedback Loop from Our Customers

    Being direct manufacturers, we’re on the frontlines of what works and what doesn’t. We receive feedback after every major lot, and we notice patterns as customers share both successes and troubles. A feedback-driven improvement process led us to adjust our drying sequence after a large R&D synthesis campaign highlighted minor hydrolysis in competitors’ products. Our controlled drying under inert gas solved the issue before the next quarterly run, and subsequent customer trials saw zero hydrolysis in their functional dye syntheses.

    We take requests for enhanced analytical data seriously. Researchers and process chemists need batch-consistent FTIR, HPLC, and GC traces, so we keep archives of all batch records and provide custom analyses upon request. In regulated sectors, such as active pharmaceutical intermediates, we share validated impurity profiles and full trace data. Years of hands-on manufacturing means we see not just the numbers but the context—a chromatographic spike or subtle color difference can mean more to a process chemist than a stack of paperwork.

    Challenges and Forward-Looking Improvements

    Every chemical process brings new hurdles. Synthesis of 4-Acetylamino-2-(Diallylamino)Anisole sometimes presents challenges with catalyst fouling and maintaining clean reaction conditions at larger scales. Drawing on in-house R&D, we transitioned from legacy acid-catalyzed methods to controlled pH, solvent-free processes that produce consistent output with greener metrics. Heat management and in-line purification ensures the product consistently meets our standards, driving both cost savings and new confidence for downstream users.

    There remains a constant need to reduce process solvent residues, align with new regulatory regimes, and boost atom economy. We continue to invest in real-time monitoring, traceability from raw materials to finished drum, and digital documentation. Advancing these protocols has allowed us to preempt many compliance headaches and makes batch recall or supply chain verification smoother for buyers focused on quality or regulatory compliance.

    We participate in ongoing discussions with peers in the manufacturing sector and research collaborators, seeking out new process optimization approaches and responding quickly to analytical reporting needs. These direct exchanges have allowed us to incorporate improvements and implement customer suggestions, such as integrating new drying technology, or adopting more sustainable feedstock sourcing without compromising quality.

    Why Direct Manufacturer Experience Matters

    Purchasing directly from the manufacturer brings benefits beyond the price per kilogram. User needs get heard and incorporated into ongoing production changes. If a customer’s analysis reveals an impurity at sub-ppm levels that impacts reaction scaling, we work with them to hunt down the source and adjust our pre-filtration or purification accordingly. Partners have sent us end-use feedback that feeds directly into process optimization, be it adjusting storage, refining drying times, or updating purity thresholds for modern applications.

    Our presence throughout the entire value chain, from raw substrate purification to final lot-specific documentation, lets us give technical support rapidly and accurately. We do not rely on off-the-shelf information or inherited process limitations. Materials handed over to users are designed with their end requirements in mind, because we process, test, and ship every batch ourselves.

    Continuous Investment in Quality and Traceability

    Over time, we have invested in advanced batch tracking software and introduced sensor-based lot recording to identify and prevent mixing errors. This reliability stays central as market demands climb for transparency and traceability. Clean documentation lets buyers trace their product origins, satisfying both internal quality checks and the increasing array of global regulations linked to chemicals of higher concern.

    We keep a continuous archive of batch details, not simply for compliance but to respond to customer audits or technical troubleshooting with full chemical history. Reviewing usage patterns has led us to fine-tune logistical planning, helping us supply large users at steady intervals to avoid stockouts, even during global supply chain swings.

    Real Impact in the End-Use Environment

    Ultimately, the best measure of a specialty chemical is how it performs where it counts. Production batches of 4-Acetylamino-2-(Diallylamino)Anisole from our site enter new pigments for automotive or textile coloring, complex intermediates in next-generation drugs, and advanced imaging materials. At the factory, these downstream applications push our team to refine quality—whether that means switching filtration media, improving drum sealing, or verifying certification for overseas markets.

    We are committed to keeping the line open with our clients—sharing new findings, refining production as needs change, and standing accountable for every gram produced. Years of chemical know-how and customer collaboration have established our 4-Acetylamino-2-(Diallylamino)Anisole both as a technical mainstay and as a springboard for future discovery.