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N,N,3,5-Tetramethylaniline

    • Product Name N,N,3,5-Tetramethylaniline
    • Alias 2,4,6-Trimethylaniline
    • Einecs 211-181-2
    • 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

    101979

    Product Name N,N,3,5-Tetramethylaniline
    Cas Number 24544-04-5
    Molecular Formula C10H17N
    Molecular Weight 151.25 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 238-240 °C
    Melting Point -2 °C
    Density 0.94 g/cm³
    Flash Point 101 °C
    Solubility In Water Slightly soluble
    Refractive Index 1.535
    Synonyms 3,5-Dimethyl-N,N-dimethylaniline
    Smiles CC1=CC(=CC(=C1)N(C)C)C
    Purity Typically ≥ 98%
    Storage Temperature Store at room temperature

    As an accredited N,N,3,5-Tetramethylaniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250 g amber glass bottle with secure screw cap, labeled "N,N,3,5-Tetramethylaniline, 98%," hazard and safety symbols displayed.
    Shipping N,N,3,5-Tetramethylaniline should be shipped in tightly sealed containers under cool, dry, and well-ventilated conditions. It must be protected from heat, sparks, and open flames. Label containers appropriately and comply with relevant regulations for transporting chemicals. Ensure shipping documents detail hazards, and emergency procedures are provided for safe handling during transit.
    Storage N,N,3,5-Tetramethylaniline should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Keep it away from heat and sources of ignition. Store at room temperature, and protect from light and moisture. Proper labelling and secondary containment are recommended to prevent accidental exposure or leaks.
    Application of N,N,3,5-Tetramethylaniline

    Applications of N,N,3,5-Tetramethylaniline in Industrial Manufacturing

    N,N,3,5-Tetramethylaniline is established in specialized chemical synthesis for high-value industrial sectors. As a direct manufacturer, we support formulation development and large-scale production for advanced organic and materials downstream markets. The following application scenarios detail integration pathways and recognized regulatory frameworks.

    1. Intermediate for Azo Dye Synthesis

    Many dye manufacturers formulate N,N,3,5-tetramethylaniline as a key aromatic amine component during diazotization and coupling steps to produce high-purity azo dyes. Its methyl substitution pattern enables retarded oxidation, resulting in deeper, more stable yellow and orange shades. Compliance with environmental and textile industry standards mandates precise control of amine content and side products at each process stage. Custom blending of this raw material ensures batch reproducibility for textile coloration and printing inks.

    Industry compliance standards

    • OEKO-TEX® Standard 100 Annex 6 (textile chemicals)
    • ZDHC MRSL V3.1 (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • REACH Regulation (EC) No 1907/2006—Aromatic Amines Limitations
    • ISO 105-C06 (Textiles—Tests for Color Fastness)

    Typical usage ratio

    • 5–15% mole ratio relative to diazotization base, adjusted by final dye chromophore target and reactivity of other intermediates

    Downstream process integration

    • Charged after solvent charging and pre-cooling, before slow basification for diazotization
    • Batched inline with sulfonating and molecular coupling reactors
    • Inline monitoring for residual amine and color development

    Final product types

    • Reactive azo dyes for cellulosic fibers
    • Disperse dyes for polyester finishing
    • Textile pigment dispersions
    • Industrial printing colorants

    2. Precursor for High-Performance Pigment Manufacturing

    Pigment producers utilize N,N,3,5-tetramethylaniline to generate specific di-amino compounds that serve as building blocks for high-temperature, color-stable organic pigments. The precise substitution reduces migration and improves ultraviolet resistance of finished pigments used in automotive and coil coating systems. Raw material conformance to established pigment synthesis specifications is critical for minimizing impurities and securing end-use certifications for coatings.

    Industry compliance standards

    • ASTM D3723 (Organic Pigments Quality Control)
    • EN 71-3:2019 (Safety of Pigment Materials—Migration of Certain Elements)
    • ISO 18451-1 (Pigments and Extenders Terminology)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances in Electrical and Electronic Equipment)

    Typical usage ratio

    • 10–25% by total weight of aromatic precursor input, tailored by pigment series, desired chromatic properties, and polymer compatibility

    Downstream process integration

    • Functionalized in condensation synthesis after initiation of the base aromatic scaffold
    • Pigment reactors dose the material with continuous temperature and pH control
    • Critical timing into azo coupling or cyclization steps to finalize pigment structure

    Final product types

    • Heat-resistant organic pigments for plastics
    • Automotive paint pigment bases
    • Coil coating colorants for metal processing
    • Printing ink pigment concentrates

    3. Component in Advanced Polymer Antioxidant Production

    Producers of polymer stabilizers employ N,N,3,5-tetramethylaniline as a specific intermediate for synthesizing hindered amine antioxidants. Its structural features permit efficient derivatization, leading to long-term oxidative stability in polyolefin, polyurethane, and engineering polymer applications. Batch-to-batch consistency is controlled during amination and ring closure phases to satisfy global automotive, packaging, and consumer goods safety requirements.

    Industry compliance standards

    • EU Regulation (EC) No 10/2011 on Food Contact Plastics
    • ISO 9001:2015 (Quality Management Systems—Polymer Additive Manufacturing)
    • UL 94 (Flammability of Plastic Materials for Parts in Devices and Appliances)
    • FDA 21 CFR 177.1520 (Olefin Polymers—Food Additives)

    Typical usage ratio

    • 5–20% of total secondary amine source input in antioxidant precursor blend; varied by desired stabilization effect and resin type

    Downstream process integration

    • Fed following initial catalyst addition in staged reactor systems
    • Introduced during ring closure and functional group protection steps
    • Subject to in-process sampling to confirm derivative formation and residual amine removal

    Final product types

    • Hindered amine light stabilizers (HALS) for PP, PE, PU
    • Polymer masterbatch stabilizers
    • Composite film antioxidants for food and industrial packaging
    • Automotive exterior polymer additives

    4. Intermediate for Agrochemical Active Ingredient Synthesis

    Agrochemical companies use N,N,3,5-tetramethylaniline as a derivatization point in multi-step syntheses for selective herbicides and plant growth regulators. Its methyl branches enhance lipophilicity and influence bioavailability. Consistent product quality and low-impurity profile remain central for meeting pesticide registration and residue compliance benchmarks. Reaction purity and critical impurity data are supplied per lot to support downstream regulatory filings.

    Industry compliance standards

    • FAO/WHO JMPR (Joint Meeting on Pesticide Residues) Guidelines
    • OECD Good Laboratory Practice (GLP) for Agrochemical Synthesis
    • ISO 17025 (Testing and Calibration for Agrochemical Laboratories)
    • BPR Regulation (EU) No 528/2012 (Biocidal Products Regulation)

    Typical usage ratio

    • 10–18% of total stepwise aromatic amine content in key synthesis phases; tailor ratios based on target active ingredient structure and endpoint purity specification

    Downstream process integration

    • Injected after fundamental ring activation and halogenation in stepwise agrochemical synthesis
    • Core functional group introduction during linker chemistry, ahead of final methylation
    • Monitored for selectivity and avoidance of dimerization by-products

    Final product types

    • Selective herbicide actives
    • Plant growth regulators with methylamino groups
    • Agrochemical technical concentrates (TC)
    • Wettable powder and emulsion agro-formulations

    5. Synthesis of High-Purity Specialty Chemicals for Electronic Materials

    Electronics manufacturers specify N,N,3,5-tetramethylaniline to synthesize high-purity intermediates for organic semiconductors, especially where electron-donating substituents are needed. Stringent control of trace metals and residual base components is upheld throughout production to meet tight electronic-grade purity thresholds. Raw material batches achieve laboratory validation for integration into OLED, photoresist, and sensor substrate material production.

    Industry compliance standards

    • IPC-4552A (Electronics Industry Standards—Organic Material Qualification)
    • JEITA ET-7304 (Control of Minor Elements in Organic Electronic Materials)
    • IATF 16949:2016 (Quality Management for Automotive Electronics)
    • IEC 61249-2-7 (Requirements for Base Materials—Electronic Circuits)

    Typical usage ratio

    • 8–15% by mass in organic semiconductor precursor batch; optionally reduced for thinner layer deposition or to minimize residual by-products in downstream vacuum applications

    Downstream process integration

    • Dosed at precision metered feed into condensation and functionalization steps
    • Introduced prior to column purification for removal of non-aryl amine impurities
    • Inline HPLC analysis at each process hand-off

    Final product types

    • OLED (Organic Light Emitting Diode) intermediate materials
    • Photoresist precursor chemicals
    • Advanced organic thin-film transistors (OTFTs)
    • Sensors and low-voltage electronic substrate materials
    Free Quote

    Competitive N,N,3,5-Tetramethylaniline prices that fit your budget—flexible terms and customized quotes for every order.

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    Certification & Compliance
    More Introduction

    N,N,3,5-Tetramethylaniline: Developing Confidence in Consistent Aromatic Amines

    Grounded Expertise from a Chemical Producer's Bench

    We rarely see technical texts match the nitty-gritty reality of running a dye or pharmaceutical synthesis department. As direct manufacturers deeply engaged with aromatic amines, we've learned that product consistency emerges only through hands-on process control and ongoing adaptation. N,N,3,5-Tetramethylaniline, as a selective aromatic amine, finds its strongest role where chemical reactivity and high-purity demands collide, and we've applied our practical know-how to refine every batch that leaves our reactors.

    What Our N,N,3,5-Tetramethylaniline Offers

    We manufacture N,N,3,5-Tetramethylaniline using a tightly monitored methylation process. Over time, we have standardized optimal conditions to control side products and ensure high purity. The compound's clear, pale-yellow liquid form remains stable under sealed environments––a benchmark we've hit through careful distillation and monitored storage. We run regular GC and HPLC checks, and every truckload that leaves our facility reflects the day-to-day diligence of refinery teams, not just paperwork assurances.

    Chemically, this product stands out for its four methyl groups, located at two nitrogen positions plus carbon positions 3 and 5 on the ring. That unique arrangement makes it a distinctive signaling tool for downstream chemists. We’ve seen how its structure blocks certain electrophilic substitutions, keeping reactivity manageable even for less-experienced hands on the production floor. Out in the field, this means better batch-to-batch reliability, especially where selectivity plays a critical role.

    Lessons Learned: Downstream Application and Real-World Compatibility

    After decades producing aromatic amines, we’ve noticed some common pitfalls in process chemistry. For those pushing R&D or scaling up, a subtle shift in methyl group positions can throw off yields or trigger hard-to-separate side streams. Our N,N,3,5-Tetramethylaniline follows tight control of isomeric impurities. We’ve had feedback from resin and pharmaceutical clients: a minor contamination with positional isomers can stall a plant for days, which explains our attention to raw material sources and high-vacuum equipment maintenance. In practice, the learning curve never ends—analytical improvements and input from the end-users keep driving our refinements here.

    This product slots in where you need amines that aren't as electron-rich as plain N,N-dimethylaniline, but that outperform toluidines in terms of both purity and reactivity. Such chemical nuance only arrives from repeated process optimizations on-site, not just from supplier catalog promises. We balance the methylation ratios, reactant purity, and temperature profiles ourselves. If a step causes minor discoloration, we tweak solvents and agitation patterns accordingly, based on daily operator feedback.

    Specific Usage in Dyes, Drugs, and Polymers

    We’ve seen N,N,3,5-Tetramethylaniline perform reliably in dye intermediate manufacturing, particularly where color strength and clarity rely on starting material smoothness. As an amine, it’s carved out utility in azo dye synthesis where methyl group bulk shields the ring from undesired oxidations. Customers in pigment manufacturing benefit from this, since less waste byproduct means lower wastewater treatment loads and improved final color brightness. It’s no accident—our own trials have taught us just where our process makes a difference in color stability.

    For pharmaceutical intermediates, formulation chemists look for both high purity and a well-characterized impurity profile. This compound’s robust methylation creates a controlled electron environment, supporting preparations that require precise molecular interactions. On several occasions, we’ve received requests to adjust residual water and halide content for specific reactions—something we can only deliver because we oversee our reactors and QA in-house, allowing rapid iteration and customized lots that fit real workflows.

    Comparing N,N,3,5-Tetramethylaniline With Familiar Alternatives

    Having produced a range of alkylated anilines, we can say with confidence how key differences play out. Plain aniline lacks the electron-donating bulk that methyls deliver; as a result, side reactions can run rampant under standard conditions. The N,N-dimethyl analog behaves as a more reactive base, but its selectivity in certain syntheses leaves much to be desired. Toluidines, as mono-methylated amines, provide slightly improved reactivity, but chemists often run into trouble with symmetrical coupling or color inconsistencies in dye applications.

    N,N,3,5-Tetramethylaniline bridges a gap between electron-rich and standard amines. With methyl groups crowded at both nitrogen and aryl positions, the molecule blocks access for many oxidants and discourages secondary alkylation. Out in the field, we’ve seen the real benefit: cleaner downstream separations and fewer headaches when isolating target intermediates. Our blended experience in maintenance, batch record keeping, and troubleshooting lets us predict when alternative amines will cause yield drops and inconsistent crystallization.

    Building on Process Experience: Managing Supply and Quality Year over Year

    Years of monitoring raw material reliability have shaped every decision in our synthesis planning. We’ve faced supply interruptions for feedstock like xylene and methylating agents. In response, our procurement teams work directly with refineries, keeping dollar swings and off-spec shipments to a minimum. Any shift in the quality of upstream chemicals—trace iron, water, or halides—can ruin a batch’s usability downstream. The closest analogy we can offer isn’t from a textbook but from standing over a troubled reactor on a damp winter morning, tracing back each raw material lot number until the root cause comes out.

    Consistent N,N,3,5-Tetramethylaniline requires entering every process run with fresh material analysis, not just batch records. By getting our production managers and GC analysts into real conversations, we attach corrective steps to every blip in chromatographic patterns. If a downstream user flags an odd UV-vis signature or an unexpected melting point, our QA group digs through data points and actual bench trials, not just formal paperwork or standard checklists.

    Regulatory, Environmental, and Safety Considerations from a Manufacturer’s Perspective

    In decades of operation, our teams have felt the push and pull between operational efficiency and environmental responsibility. Our approach to N,N,3,5-Tetramethylaniline sets safety at the point of production, not just regulatory compliance boxes. Operators train regularly to handle liquid amines under negative pressure hoods and check ventilation in real time. We upgraded our waste streams so that even low-level amine emissions meet not just current air control laws but the real standards we hold for neighborhood well-being. Anyone who's spent time cleaning a fume hood or wrestling with chemical odors understands there are no shortcuts here.

    Through our in-house R&D group, we've reduced process residuals, cutting energy usage per kilogram. Even with steady demand from pigments and pharmaceutical preparations, our strategy revolves around smaller, more frequent batches instead of massive, unresponsive campaigns. That’s come from making mistakes on large runs long before anyone handed us a sustainability certificate. For site safety, we rely on soft skills as much as on PPE and sensors—knowing when to pull a team from a warm-up line or when to shut down mid-load. This lived caution seeps into the reliability of every lot of N,N,3,5-Tetramethylaniline we prepare.

    Supporting User Troubleshooting and Adaptation in Real Time

    Synthetic chemists often need to adjust reaction times and temperatures as batch characteristics shift. We do not handwave away minor deviations as “within norm.” Instead, our technical support works from field usage reports, not marketing narratives. We've spent many hours guiding downstream clients—sometimes by phone, sometimes by sharing in-lab notes—to resolve minor color shifts or optimize solvent compatibility. These cooperative runs lead to process updates at our side, driving tangible improvements. We’ve helped users swap out legacy amines for N,N,3,5-Tetramethylaniline through practical trials and have documented real savings in filtration downtime and solvent use as a result.

    Sometimes a prospective client approaches, uncertain if this molecule fits a legacy process. Our in-house chemists can share years’ worth of bench notes and anonymized case histories, detailing side-product management and process swaps. This honest information exchange often uncovers alternative preps, allowing the user to gauge economic and safety tradeoffs with full clarity. Where application experts want to dial in a precise boiling range or adjust moisture content beyond typical shipment specs, our technical and production teams meet to adjust the process within a single work week. Such flexibility comes only from deep familiarity with both our own plant and the problem-solving needs of end users.

    Real-World Value Versus Commodity Offerings

    We see plenty of low-cost aromatic amines on the global market. They tempt buyers who chase price and overlook process yield and field reliability. In reality, an “off” product—impure or unstable—can shut down an entire finishing line and push treatment costs through the roof. Our operation has dealt with the fallout of choosing cheaper feedstocks: gummy reactors, split product streams, and missed delivery deadlines. It’s this background that keeps us returning to vigilance, in sourcing, QA, and bulk tank loading.

    Feedback loops between shipping and production matter more than catalog labels or one-time audit scores. If documented impurities in other products cross the threshold for downstream toxicity or stability, that trouble lands on a technician’s bench, not an accountant’s desk. So our staff track field reports, adjusting line procedures, and documentation in step with feedback. Reliability built into every shipment of N,N,3,5-Tetramethylaniline stems from this continuous improvement mindset, unbroken by trendy outsourcing or audit-driven shortcuts.

    Innovating While Preserving Core Reliability

    Many of our longtime team members have backgrounds in dye and fine chemical synthesis. Their insight surfaces in small but vital process tweaks, from anti-corrosion upgrades on reactors to quicker phase separation at the workup stage. Investment in new sensors or lab automation is only worthwhile once proven over months of steady operation and validated by field performance. Every new equipment purchase and workflow change must pay dividends in product reproducibility, not just laboratory novelty. Over time, this blend of cautious innovation and seasoned methodology delivers a consistent N,N,3,5-Tetramethylaniline that busy downstream labs rely upon.

    Our R&D efforts track closely with customer troubleshooting needs. Field tests with emerging pigment blends or experimental pharmaceutical pathways feed directly into process upgrades. We have stopped production lines upon new evidence of impurity profiles uncovered in downstream analytical spectra, even if paperwork suggested “within spec.” This feedback and correction approach anchors our company culture, setting us apart from traders and general resellers who rarely witness the day-by-day implications of even a singular batch deviation.

    Building Trust Through Deep Chemical Understanding

    Trust develops in the trenches, not on marketing copy. Engineers and technicians in our team have built their careers on recognizing the subtle shifts—pH, color tone, gas evolution—that determine whether a kilogram batch of N,N,3,5-Tetramethylaniline will lead to a productive plant run or an unplanned maintenance slog. Many of our best process improvements trace back to direct calls from end users who noticed a reduction in reaction yield or a sudden foaming in their blending tanks. The mutual respect forged in these exchanges leads to honest communication and process transparency, rather than the abstract assurances so common in bulk chemical sales.

    Years of refining this molecule’s production—from methylating agent ratio controls to multimodal impurity analysis—allow us to meet shifting industry expectations. This isn’t the byproduct of outsourced QA or generic standards; it’s a function of crews monitoring reactors at 3 am, troubleshooting pilot runs before breakfast, and chasing fractions through columns in real time. Through honest feedback and technical curiosity, we have shaped the reputation of our N,N,3,5-Tetramethylaniline, making it a trusted ally of bench scientists and process engineers aiming for reliable syntheses at scale.

    The Manufacturer’s Commitment

    Direct connection to both the product and its downstream users breeds a kind of pride bigger than a certificate or audit pass. Our commitment to N,N,3,5-Tetramethylaniline is rooted in day-by-day attention and hands-on learning, not just contractual obligation. In the moments where a customer faces a tricky yield or an unpredictable impurity, our willingness to roll up our sleeves and dig in separates us from catalog-driven or trading-focused suppliers.

    We continue to invest in both our people and our manufacturing infrastructure—with an eye toward real-life problem solving. Whether you’re running a large industrial batch, piloting a new shade in dye chemistry, or trailblazing in medicinal innovation, our experience with aromatic amines brings daily lessons to bear on every order and every request. For those whose work depends on honest chemical consistency and rapid, informed support, our N,N,3,5-Tetramethylaniline stands ready, shaped by years of shared effort and mutual accountability.