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4-Amino-N,N-Dimethylaniline

    • Product Name 4-Amino-N,N-Dimethylaniline
    • Alias N,N-Dimethyl-4-phenylenediamine
    • Einecs 202-109-0
    • 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

    140403

    CAS_Number 586-50-7
    Molecular_Formula C8H12N2
    Molar_Mass 136.19 g/mol
    Appearance Gray to brown crystalline solid
    Melting_Point 53-56 °C
    Boiling_Point 266 °C
    Density 1.06 g/cm³
    Solubility_in_Water Moderately soluble
    pKa 5.1 (for the amino group)
    Synonyms p-(Dimethylamino)aniline, p-Amino-N,N-dimethylaniline

    As an accredited 4-Amino-N,N-Dimethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of 4-Amino-N,N-Dimethylaniline is supplied in a sealed amber glass bottle with hazard labels and clear product identification.
    Shipping 4-Amino-N,N-Dimethylaniline is shipped in tightly sealed containers, protected from light and moisture. It must be clearly labeled as hazardous, following all regulatory requirements. Transport should occur via approved carriers with appropriate documentation, ensuring the chemical is handled and stored away from incompatible substances and under controlled temperature conditions.
    Storage 4-Amino-N,N-dimethylaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from sources of ignition, heat, and incompatible substances such as strong oxidizers. Protect from light and moisture. Ensure proper labeling, and avoid storing near food or drink. Follow all relevant safety regulations and use secondary containment to prevent spills.
    Application of 4-Amino-N,N-Dimethylaniline

    Applications of 4-Amino-N,N-Dimethylaniline in Industrial Manufacturing

    As the direct producer of 4-Amino-N,N-Dimethylaniline, we support key sectors that rely on this intermediate in their established workflows. The following application scenarios show where manufacturers have integrated this compound for its chemical reactivity and specificity, using controlled processes and meeting established global requirements for quality and compliance.

    1. Dye and Pigment Intermediates for Textile Manufacturing

    Textile dye producers incorporate 4-Amino-N,N-Dimethylaniline as a coupling component in the synthesis of azo dyes, especially for producing deep-blue and greenish-shade colorants. This material enables manufacturers to formulate stable, colorfast dyes, which are subsequently applied to cotton, wool, and synthetic fibers via high-temperature and high-pressure dyeing lines. Integration requires precise control in diazotization and coupling steps, ensuring batch-to-batch consistency and compliance with environmental discharge limits on aromatic amines.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex 4 restricted substances (European Union)
    • GB/T 17592-2011 Determination of banned azo colorants (China)
    • REACH Regulation (EC) No 1907/2006—Appendix 8 restrictions
    • ZDHC MRSL—Zero Discharge of Hazardous Chemicals List

    Typical usage ratio

    • 2.5–6.0% by molar ratio relative to total diazo component in dye synthesis; exact proportion tailored by shade, depth, and fabric compatibility requirements.

    Downstream process integration

    • Added during the coupling stage of the azo dye production workflow after primary diazotization, ensuring the specific amine reactivity for target color.

    Final product types

    • Reactive dyes for cellulosic fibers (cotton, viscose)
    • Acid dyes for protein fibers (wool, silk)
    • Direct dyes for blended textile goods
    • Non-migrating pigments for printing inks

    2. API Synthesis for Pharmaceutical Intermediates

    Pharmaceutical manufacturers utilize this amine as a precursor in the synthesis of specific Active Pharmaceutical Ingredient (API) intermediates, including anesthetic agents and antihistamines. Stringent GMP production lines demand high-purity grades for reaction specificity and minimization of nitrosamine content, with in-process analytical controls at every stage. Selection and dosage depend on downstream molecule structure, with integration in controlled hydrogenation and acylation steps to achieve defined pharmaceutical moieties.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidelines for APIs
    • USP–NF (United States Pharmacopeia–National Formulary) impurity thresholds
    • EDQM CEP (European Directorate for the Quality of Medicines—Certificate of Suitability)
    • Ph. Eur. 2.4.24—Nitrosamine impurities

    Typical usage ratio

    • 0.8–1.2 equivalents to key acyl halide or aldehyde substrates in API intermediate formation; adjusted upon yield optimization and regulatory impurity limits.

    Downstream process integration

    • Dosed into the amination or alkylation stage of fine chemical synthesis, followed by isolation and purification under GMP-compliant protocols.

    Final product types

    • Pharmaceutical intermediates for anesthetic agents
    • Precursor compounds for antihistamine synthesis
    • Building blocks for specialty bulk drugs
    • High-purity intermediates for regulated final APIs

    3. Polymer Stabilizer Additives in Plastics Manufacturing

    Producers of specialty thermoplastics employ this compound as a precursor in synthesizing certain hindered amine light stabilizers (HALS) that extend the lifetime of polyolefin and polystyrene materials. Its amine structure introduces UV resistance and radical scavenging functionality, which downstream polymer processors incorporate during compounding and extrusion stages. Use levels depend on stabilizer formulation, resin matrix, and end-use outdoor exposure requirements, while production lines monitor additive dispersion and extraction resistance.

    Industry compliance standards

    • ISO 4892-2 Weathering testing for plastics
    • FDA CFR 21 177.1520 (Polypropylene and polymers—additive approvals for food contact, US)
    • EU Regulation No 10/2011 on plastic materials for food contact
    • ASTM D2565 UV resistance test standards

    Typical usage ratio

    • 0.05–0.2% (w/w) as incorporated HALS precursor, with dosage optimized by polymer grade, required UV stability, and regulatory migration limits.

    Downstream process integration

    • Firstly reacted with alkylating or acylating agents on-site to form the target stabilizer molecule, then added during molten resin blending or directly into masterbatch production lines.

    Final product types

    • UV-stabilized polypropylene and polyethylene films
    • Weather-resistant polystyrene sheets
    • Industrial masterbatches for extrusion and molding
    • Plastic parts for outdoor applications

    4. Electrochemical Functionalization in Imaging and Photographic Chemicals

    Imaging industry manufacturers rely on 4-Amino-N,N-Dimethylaniline as a developer component and functional intermediate in color coupler synthesis for photographic and radiographic materials. It provides precise redox activity and color-forming properties in silver halide processing solutions. Formulators adjust ratios to ensure image sharpness, contrast, and developer life span, with tight controls on byproduct formation and batch reproducibility. Compliance focuses on minimizing contaminant carryover and alignment with international imaging material regulations.

    Industry compliance standards

    • ANSI IT9.2 Image Stability Test Methods
    • ISO 18911 Imaging materials—Processing chemicals
    • RoHS Directive—Heavy metal content (where used for electronic media)
    • EN 60950-1:2006 Imaging and photochemical safety standards

    Typical usage ratio

    • 0.1–0.8% (w/v) in developer concentrate formulations, adjusted for emulsion sensitivity, process speed, and required image properties.

    Downstream process integration

    • Introduced in the color developer preparation tank, followed by mixing with alkali and buffer, then used in continuous photoprocessing lines or batch systems.

    Final product types

    • Color photographic paper and film developer concentrates
    • Radiographic imaging developer solutions
    • On-site processing kits for analog photo labs
    • Fine grain imaging emulsions

    5. Chemical Sensor and Analytical Reagent Synthesis

    Specialty chemical laboratories and analytical reagent manufacturers employ this compound for synthesizing colorimetric and electroactive reagents used in water quality, trace metal, and oxidative stress detection. Its functionalization in target reagents yields selective chromophores or electron mediators, with usage rates and process steps governed by the sensitivity and specificity requirements of the end test. Compliance confirms reagent batch purity and storage stability, with tight monitoring of background impurity levels for trace analysis.

    Industry compliance standards

    • ISO/IEC 17025 General requirements for the competence of testing laboratories
    • EN 1483 Determination of mercury (application in spectrophotometric assays)
    • EPA Method 218.6 for colorimetric silica analysis
    • DIN 38405 Analytical water testing standards

    Typical usage ratio

    • 0.02–0.2% (w/v) in analytical reagent mixes; levels refined according to detection range, matrix effect, and sensitivity targets of the final application.

    Downstream process integration

    • Converted on-site into the desired chromogenic or electron-transfer agent via diazotization or condensation, then incorporated into ready-to-use analytical reagent kits or sensor test strips.

    Final product types

    • Spectrophotometric water analysis kits
    • Colorimetric reagents for trace analyte detection
    • Reagent-embedded sensor strips
    • Standardized reference solutions for laboratory QA
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    Certification & Compliance
    More Introduction

    4-Amino-N,N-Dimethylaniline: A Closer Look from the Manufacturer’s Desk

    Understanding 4-Amino-N,N-Dimethylaniline and Its Unique Role

    4-Amino-N,N-Dimethylaniline stands as a distinct aromatic amine known for its versatility and chemical resilience in demanding applications. Working directly in chemical synthesis every day, we see how its unique methylated structure changes everything about its reactivity and performance compared to simpler aromatic amines. This compound, recognized by its CAS number 99-98-9 and chemical formula C8H12N2, brings a different dimension to both large- and small-scale manufacturing processes. Our experience as direct producers means every batch leaving the facility reflects careful refinement and solid process control based on real-world usage, not just theoretical formulary.

    Direct Experience with Technical Specifications

    We focus on the production of 4-Amino-N,N-Dimethylaniline in a high-purity crystalline or powder form, ensuring every particle reflects our in-house standards. Most requests call for a minimum purity above 99%, since impurities, particularly from incomplete methylation or parallel side-chain reactions, cause headaches further down the production line. As someone who sees the synthesis on the shop floor, watching those subtle differences in melting point or color prove critical during large scale crystallization batches. Differences as slight as a tenth of a degree Celsius or a hint of color change often point to earlier process deviations.

    By carefully monitoring the methylation steps, we caught early problems that others might overlook. Equipment scale-up brought its own challenges, as flow rate, temperature gradients, and pH control impact final product quality. Technical data collected daily—melting point, residue on ignition, loss on drying, and solution coloration—comes more from practical needs than any external standard. Many international clients appreciate our willingness to share not just COAs, but the story behind each lot.

    Application Insights from Years on the Plant Floor

    Over the years, chemists, engineers, and production managers have shared their feedback with us on what matters most in using 4-Amino-N,N-Dimethylaniline. Its pivotal role as an intermediate in the manufacture of dyes jumps out right away, especially for those in azo and anthraquinone colorant synthesis. Because it holds two methyl groups on the aniline nitrogen, its reactivity differs significantly from either plain aniline or mono-methylated forms. These methyl groups carry more than just steric effects; they modulate the electron density, shifting reaction yields and affecting reaction selectivity.

    End users notice that color strength and fastness properties in pigments reflect the purity of their intermediates. Textile dye manufacturers have pointed out fewer color inconsistencies and less batch-to-batch adjustment when using material produced to tighter controls. In laboratory-scale synthesis, researchers have shared data illustrating the advantages of reproducible amine alkalinity and lower background impurities, which often means improved yield in pilot run-ups.

    We also serve forensics and specialty chemical producers who value low residual moisture and organic volatiles. Even a modest shift in side impurities from alternative synthetic routes ends up skewing high-value analytical readings. Our manufacturing line holds to a regime of controlled pH and individually-verified washing steps. Instead of just relying on automated washing cycles, our process operators test effluent until it consistently reads clean, often going beyond simple SOPs for that extra measure of quality.

    Key Differences from Similar Amines

    Many customers—old hands and newcomers alike—want to know how 4-Amino-N,N-Dimethylaniline fits into their line compared to more basic amines such as aniline, or even mono-methylated variants such as N-Methylaniline. The answer, based in years of handling all three, comes down to how methyl substitution modifies both reactivity and process safety.

    First, 4-Amino-N,N-Dimethylaniline arranges its methyl groups on the nitrogen, making it less prone to undesired oxidation during storage. We’ve found that barrels stored under identical conditions show a marked difference in color stability compared to non-methylated amines, which often yellow or darken quickly. This matters not just for shelf life, but also for final product consistency.

    Next, difference in nucleophilicity, solubility, and reduction potential often goes overlooked until a pilot batch produces unexpected byproducts. Double methylation dampens nucleophilicity, which is an advantage in processes sensitive to over-reaction. Using this compound as a coupling agent in dye synthesis, for instance, allows for greater precision without the runaway side reactions found with more reactive analogues.

    Process engineers have noticed that reactions requiring selective functionalization benefit from this compound’s reduced basicity and lower tendency to form tars or other insoluble residues, especially during catalytic steps. We’ve optimized filtration and purification stages based on years of feedback from end users who struggled with filtration bottlenecks on other aromatic amines.

    From a safety and environmental perspective, storage and transport risk is also lower than more reactive analogues, thanks to reduced sensitivity to light and atmospheric oxygen. During high-humidity periods, we’ve seen that our product resists clumping better, largely due to the careful drying and controlled particle size from our custom milling units.

    Common Questions: Usage in Synthesis and Safety Handling

    Demand for 4-Amino-N,N-Dimethylaniline has grown not just in dyes, but in active pharmaceutical intermediate and agrochemical development, where its methyl groups prevent unwanted metabolic breakdowns in later derivatives. Process chemists have reached out to us for advice on solvent systems, and through hands-on batch trials, we’ve found that polar aprotic solvents tend to provide better yields and reduce impurity carryover, helped in part by the compound’s altered solubility profile.

    During scale-up, several customers have faced foaming or exothermic events common to other amine synthons. Our in-plant R&D team has worked through customized quenching protocols and staged addition procedures, sharing our insights on heat management and effluent neutralization. This support flows from the kind of close, long-term relationships a manufacturer can build, not the more transactional approach seen in trading intermediaries.

    On safety handling, our perspective differs from a distributor’s. Process operators at our site don’t just glance at an MSDS—they rely on firsthand experience. Our chemical safety team works alongside operators to design local exhaust and engineering controls that prevent fume formation, recognizing that even low-molecular-weight amines can pose inhalation risks. Good quality raw materials, handled by trained staff using experience-based protocols, make a difference in reducing accident rates and improving plant morale.

    As a manufacturer, we track our waste streams and air emissions down to the kilogram. We have also invested in closed-drainage and automated precision weighing to keep fugitive losses as low as stochastic error margins allow, reflecting a direct link between chemical efficiency and safer, more sustainable operations.

    Practical Challenges in Manufacturing and Quality Assurance

    Bringing high-quality 4-Amino-N,N-Dimethylaniline to market requires both technical know-how and constant vigilance. Each synthesis begins with carefully sourced raw materials. We subject every incoming lot to both rapid screening and more extended impurity mapping using GC-MS or LC-MS. By catching contaminants early, we avoid compounded problems during crystallization or drying. Early years saw a fair share of batch failures due to minor variations in upstream suppliers’ aniline derivatives. Only after imposing tighter acceptance criteria and linking vendor performance to real-time analytical results did material quality reach the required consistency.

    The methylation process, typically carried out using formaldehyde or methylating agents under acidic conditions, benefits from active monitoring and tightly controlled addition rates. If reaction rates drift, unwanted Toluidine byproducts emerge, which require laborious post-synthesis removal. Our chemists recognized that keeping pH and temperature within a tight window, often monitored both in-line and by batch spot-check, minimizes waste and maximizes yield.

    After reaction completion, our material passes through multiple washings to remove salt, acid, and soluble organic residues. Many producers cut corners at this point, stopping after only a single water or acid wash. We run repeated washes, testing filtrate after each stage, and documenting results. Using centrifugation and vacuum drying, moisture gets reduced below one-tenth of a percent by weight, essential for bulk buyers using pneumatic transfer.

    Batch-to-batch consistency underpins the faith that technical buyers place in us as a manufacturer. Small swings in melting point or color, more than a matter of academic notation, affect production lines downstream. Several buyers in advanced material R&D have visited our plant specifically to audit handling practices and batch traceability, confirming for themselves that our lot histories stand up to scrutiny.

    Our stability samples regularly withstand months to years of ambient exposure testing. During each interval, we check for color shift, moisture regain, and any evidence of nitrogen oxide formation. As we have improved methods for nitrogen blanketing and packaging, shelf life has continually extended. One large volume client recently reported using our material stored for over a year, observing no measurable deterioration in their final dye color yield.

    Case Studies: How Real-World Feedback Drives Improvements

    Several customers in the dye and pigment sector highlighted purity issues when shifting from reagent-grade to technical-grade material. Their quality teams discovered discoloration on final product due to trace oxidants in poorly-washed intermediates supplied by other vendors. They turned to us for fresher, better-handled batches. We welcomed their site visits, allowing their technical specialists to follow a shipment from synthesis right through to packaging. Subsequent batches consistently met their color strength requirements, prompting expansion of the relationship.

    Another major user, involved in specialty pharmaceutical intermediates, needed specific control of isomeric purity. Their downstream biological activity was especially sensitive to ortho and meta byproducts. Our process chemists collaborated for several months, reviewing production notes and pilot scale runs, to reoptimize our crystallization steps. By modifying solvent systems and cooling rates, we managed to cut minor isomer impurities down to trace levels, confirmed by side-by-side NMR and GC-MS comparison with external standards.

    On more than one occasion, batch shipment delays due to adverse weather forced us to develop alternative backup logistics solutions. By holding extra stability samples on-site and using in-transit temperature and humidity monitoring, we guarantee the arriving product matches shipped samples. These are not just abstract supply chain exercises—they reflect the challenge and impact of managing sensitive chemicals across large geographies.

    Advances in Environmental Management

    Running a chemical plant brings more than technical accomplishment; it involves seeing waste not as a byproduct, but as a stewardship challenge. Over recent years, our investment in solvent reuse, heat integration, and closed-recirc water handling have each cut our discharge volumes and minimized resource intensity per kilogram of product.

    We deploy real-time sensors across each discharge and vent stream, generating a continual profile for internal review and external transparency. Our in-house safety team holds regular joint reviews with process staff and local authorities to fine-tune emergency response and emissions reduction. This approach goes well beyond regulatory fulfillment: it reflects the culture of accountability many of our staff expect from a manufacturer, particularly as the eyes of the world increasingly fall on sustainable sourcing.

    Responding to customer requests for Green Chemistry options, we've piloted less hazardous methylation agents. By sharing intermediate results and seeking outside feedback, process refinements have led to lower by-product formation and a smaller carbon footprint—advances most direct users find valuable in today’s more competitive environment.

    Our experience demonstrates that every sustainability effort, from waste neutralization to smart packaging, builds credibility with both regulators and end users. Chemical buyers appreciate manufacturers who share not only finished product specifications, but also a transparent window into production improvements and ongoing environmental reporting.

    Supporting Partners through Direct Technical Knowledge

    Decades in the synthesis and packaging of 4-Amino-N,N-Dimethylaniline proved to us that the best relationships form through problem-solving, not salesmanship. Clients from dye, pharmaceutical, polymer, and analytical sectors frequently call on our expertise for troubleshooting and process support, whether it's improving solubility in formulation work or scaling a laboratory finding to the plant.

    In several projects, laboratory synthesis saw simple success, but transfer to pilot or full production revealed unexpected mixing or reaction foaming. Physical plant layout, vessel sizing, and even climate control all influence final yield. By sharing not just best practices, but also war stories of our missteps and subsequent breakthroughs, we help downstream users avoid costly false starts.

    We regularly convene workshops for technical partners, bringing together process engineers, quality managers, and operational chemists to discuss real-world results with the compound. Last year’s session saw an extended discussion on analytical interference from trace impurities, with shared spectral data building groupwide knowledge and better finished products.

    Every large order includes not only a batch-specific COA but also direct contacts in our technical service team. We open production records for customer audit, supporting procurement and regulatory documentation directly. In fast-moving sectors, that kind of transparency speeds adoption and breeds confidence.

    Looking Forward: Continuous Improvement in 4-Amino-N,N-Dimethylaniline

    Remaining competitive as a manufacturer means more than running the same process year after year. Our approach to 4-Amino-N,N-Dimethylaniline focuses on refining every synthesis, analyzing byproducts and emissions data, and investing in automation without losing the hands-on knowledge that catches problems before they scale.

    Process automation helps by running tighter controls, but we never lose sight of the need for skilled operators who understand why the color, texture, and even the sound of a reaction vessel matters. Each production trial feeds data into continual improvement, whether through yield enhancement or reduction of trace impurities.

    Future advances in 4-Amino-N,N-Dimethylaniline production will undoubtedly see greener reagents, further emissions controls, and closer working relationships between manufacturer and chemical end-users. Building on a foundation of direct experience, technical rigor, and responsive customer engagement, our plant and our team shape the ongoing narrative of this useful and adaptable molecule—through every shipment, every process optimization, and every new partnership formed.