| HS Code | 836011 |
| Chemical Name | N,N-Diethyl-p-toluidine |
| Cas Number | 91-93-0 |
| Molecular Formula | C11H17N |
| Molecular Weight | 163.26 g/mol |
| Melting Point | -25 °C |
| Boiling Point | 258 °C |
| Density | 0.91 g/cm³ |
| Appearance | Colorless to pale yellow liquid |
| Solubility In Water | Insoluble |
| Flash Point | 99 °C |
| Refractive Index | 1.529 |
| Vapor Pressure | 0.13 mmHg (25 °C) |
As an accredited N,N-Diethyl-P-Toluidine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 500 mL amber glass bottle with a secure screw cap, labeled "N,N-Diethyl-P-Toluidine," includes hazard warnings and safety instructions. |
| Shipping | N,N-Diethyl-P-Toluidine should be shipped in tightly sealed containers, protected from light and moisture. It must be clearly labeled and transported as a hazardous chemical, complying with local regulations. Use of appropriate cushioning and secondary containment is recommended to prevent leaks or spills during transit. Handle only by trained personnel. |
| Storage | N,N-Diethyl-P-Toluidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible materials like oxidizing agents. Protect it from direct sunlight and moisture. Store at room temperature, and ensure it is clearly labeled. Follow all relevant safety guidelines to prevent accidental exposure or spills. |
As a direct manufacturer of N,N-Diethyl-P-Toluidine, we work with international producers across several advanced chemical sectors. Our material forms a key intermediate or reactive agent in a range of specialized industrial processes, where consistency, regulatory alignment, and integration efficiency are critical for downstream results. Below we present detailed applications by principal industry segments, with a focus on compliance, technical formulation, manufacturing procedure, and final product outputs.
The photopolymer printing industry regularly employs N,N-Diethyl-P-Toluidine as an amine co-initiator in UV-curable resin systems. Here, formulators require reliable initiation under controlled UV light, ensuring efficient free-radical generation for plate curing. Manufacturers carefully adjust the amine-to-photoinitiator ratio to match exposure conditions, print line resolution, and polymer matrix type. Quality focus remains on migration compliance, extractable content, and shelf stability for plates used in commercial and packaging printing.
Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
Dental material manufacturers integrate this amine as an accelerator in light-curing composite pastes, especially for direct restorative applications. Regulatory focus centers on biocompatibility and leachability per dental and medical device legislation. Formulation teams carefully balance accelerator loading with camphorquinone initiator to achieve rapid curing without excessive heat generation or discoloration. Material purity and traceability remain essential throughout mixing, compounding, and packaging for clinical dental use.
Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
Producers of UV-curable inks and surface coatings rely on N,N-Diethyl-P-Toluidine as a tertiary amine synergist to enhance photoinitiator response. This application demands precise ratio calculation to prevent residual odor and maintain film clarity. Compliance with stipulated migration limits and VOC directives drives tight QC, particularly in applications touching packaging and consumer-facing surfaces. The typical workflow involves pre-dispersion with pigments and resins, followed by controlled addition during ink or coating masterbatch preparation.
Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
Acrylic sheet producers use N,N-Diethyl-P-Toluidine as a room-temperature promoter for peroxide-initiated polymerization, especially in the casting of large or thick panels. The catalyst enables precise gel time control, critical for scaling and mold filling, and requires adherence to standards covering optical clarity and residual monomer content. Customization of the accelerator-peroxide ratio allows adjustment for temperature, mold complexity, and flow performance in continuous or batch operations.
Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
Our N,N-Diethyl-P-Toluidine serves as a selected amine base in certain multi-step synthesis pathways for producing active pharmaceutical ingredient (API) intermediates and excipients. Pharmaceutical process engineers use it in neutralization, salt formation, or as a phase transfer catalyst, always under rigorous GMP and ICH Q7 guidelines. Strict impurity profiling and validated trace removal after reaction step are vital. Each batch follows full documentation from in-house synthesis to downstream pharmaceutical plant shipment.
Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
Competitive N,N-Diethyl-P-Toluidine prices that fit your budget—flexible terms and customized quotes for every order.
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Chemistry rewards thorough work and careful engineering. N,N-Diethyl-P-Toluidine reflects those principles. Our plant produces this compound using years of experience refining aromatic amines for reliability and purity. You’ll find it by the chemical name N,N-Diethyl-4-methylaniline or sometimes just “DEPT.” The CAS number is 91-67-8. We have learned not to cut corners, whether we’re sourcing raw materials, controlling environmental conditions during synthesis, or handling post-reaction purification. This hands-on process keeps batch-to-batch variation minimal, which saves customers unpredictable downtime.
Most buyers receive the product as a clear, pale yellow liquid. The aroma gives a hint of its heritage—distinct but manageable with proper ventilation. Each drum we load goes through internal analysis, supported by GC and HPLC equipment, so each batch stays inside the agreed purity window, usually above 99 percent. The typical density comes near 0.94 g/cm³ at 20°C, with a boiling range between 260–270°C. Moisture, amine content, and the level of residual starting materials try to creep in, and our QC teams address them with tight process checks at multiple pressure and temperature set-points. What ends up in your line or reactor has a sharp identity and a direct purpose.
N,N-Diethyl-P-Toluidine is primarily a polymerization accelerator and an intermediate in specialty chemicals. Resin producers—especially those supplying dental, medical, and some construction sectors—value its speed and reliability in initiating free-radical processes. For our customers, the difference between a successful curing cycle and a failed batch can hinge on the stability of this amine. Precision makes or breaks a reaction, particularly where low-ppm contaminant levels impact downstream color, mechanical properties, or shelf-life. We focus on removing catalytic poisons and color bodies, aiming for a water-white liquid, not a rusty or greenish off-spec mass. This affects both continuous and batch operations.
In dental applications, N,N-Diethyl-P-Toluidine steps in as an amine co-initiator with benzoyl peroxide, activating rapid hardening in the acrylic and methacrylate resins used in dental prosthetics, restorative pastes, and some bone repair materials. Small inconsistencies in amine structure creep into the visible layer as haze or poor polish. We monitor amine congener content, keep byproducts under strict thresholds, and understand the relationship between impurity spectrum and final resin clarity. Resin and adhesive formulators have told us the difference is visible in recovery rates and in the amount of post-curing residuals their lines must remove to meet medical-grade standards.
Beyond dental, this molecule finds use as a polymerization accelerator in unsaturated polyester and acrylic systems. In marine, automotive, and tooling applications, composites depend on regular batch quality. Here, redundancy eliminates single points of failure: dual instrumentation, cross-checked logs, and trained staff who understand the consequences of letting a process drift. Stopping variability at the source—rather than patching it later—has cut critical returns for customers who struggled with floaters, bottom sludge, or viscosity spikes. N,N-Diethyl-P-Toluidine as we ship it today comes out of a workflow that is designed to match end-user demands for reaction speed without sacrificing storage stability or introducing excess amine smell into the final product.
Some buyers use this compound as an intermediate for synthesis—quinolines, dyes, and specialty agrochemicals. The requirements change. Downstream steps can reveal hidden flaws. We discuss endpoint use to adjust specs, whether the amine needs to pass stricter color or metal contamination limits, or if lower moisture improves overall yield. Sometimes, for non-cosmetic grades or less sensitive lines, a slightly broader spec saves money, but even then cuts get explained, not hidden. Customers have walked our lines, seen our batch records, and left with confidence that surprise is kept out of the equation.
Quinoline dye producers operating under pressure for tight color management ask us about factors beyond simple GC area percent. Impurities shift color points, so upstream control counts. Some applications need additional filtration, with advice on reduction techniques for metals or phenolic residues. This is where years in the chemical sector pay off: practical cleaning routes, recyclable waste streams, and knowing whether tweaking temperature, solvent, or wash protocol saves more in the long run.
Too many chemical buyers have faced frustration from packages that claim one thing and deliver another. The source of that problem often runs back through distributors and repackagers whose focus starts and ends at lowest cost, not accountability. By keeping control of our own production and relying on people trained in hands-on analysis, we eliminate rounds of mystery, untraceable blending, and weak after-sale support. This mindset began when complaining customers forced us to improve QC standards or lose business. We know the pain of popped barrels, late-night solvent leaks, off-spec shipments that sit on docks until the right papers arrive. Years of solving these problems built a simple rule: you can always trust a process you run yourself, and you can’t outsource responsibility for safety or purity.
Every batch we send leaves with its own analysis report—no cut-and-paste from old shipments. Embedded RFID and tamper-evident seals keep the chain of custody simple. We invite customer audits and hold regular supplier audits upstream because shortcuts drain reliability. Lower total cost often follows, but protecting your process stability and output quality always comes first.
Operators who use N,N-Diethyl-P-Toluidine daily value not marketing pitch but predictable drum-to-drum behavior. They need to know what happens in high-visibility fields like dental or in lower-profile work like dye intermediates. Color drift is not just a nuisance—it means batch rejection, regulatory risk, lost hours. We don’t understate the discipline needed to keep things consistent at all scales—from sample bottles to isotanks. That trust turns into shorter production runs, quicker product launches, and fewer technical complaints for end users.
Some new customers wonder if any amine with two ethyl groups and a methyl on the ring will do. Subtle chemical differences mean everything. N,N-Diethyl-P-Toluidine brings unique reactivity, color speed, and electron-rich stability compared with cousins like N,N-Dimethyl-P-Toluidine or N-Ethyl-N-Methylaniline. In technical terms, ethyl groups modulate the electron push into the ring, which sets apart how the material behaves in free-radical initiation or dye synthesis. Less technical but just as important, the “feel” of the material—the odor, how fast it yellows in storage, how sensitive it is to oxidation, and the viscosity in direct mixing with peroxides—changes batch outcomes downstream.
We field regular calls from formulators wrestling with slow or incomplete cures, with materials bought from alternate sources or supplied as generic “aromatic amine” mixes. A wrong amine changes cure rate, resin hardness, sometimes even introducing shape memory or tackiness in products where rigidity, clarity, and color hold the contract. In dye production, several positional isomers can show the same GC fingerprint at a glance, but shifted polarity, moisture levels, or formaldehyde presence can wreck a dye’s red or blue point. Downstream these differences look like fading tops, weak indigo, or even missed pH triggers during pigment precipitation.
Operators who put time into switching suppliers share stories of eased downstream filtration, fewer cleaning cycles, and increased first-pass yield after converting to well-controlled DEPT supply. Those small improvements add up to hundreds of man-hours and tens of thousands of saved material over a run—numbers that matter far more than theoretical “specification equivalence.”
Price-driven procurement sometimes tempts businesses to buy lower-purity grades or blended intermediates, hoping for a similar outcome. Real-world experience proves that trace impurities in aromatic amines, particularly those created by thermal rearrangements during sub-standard production, inhibit the very processes this molecule should accelerate. Unreacted starting materials, metal ions, or piped-in stabilizer residues act as poisons for peroxide-based initiators, breaking reaction chains and dragging down yield. In pigments, stray bases and oxidants show up as color dullness or patchiness, even after multiple refining steps.
So industry buyers increasingly look for a credible manufacturer with established QC, who stands behind every shipped lot. Our approach has moved past minimal “commodity” purity claims and open-bid trading. By focusing on repeatable, verifiable specifications matched to actual end use—from low-odor, medical-compatible resins to volume-dye intermediates—our DEPT consistently outperforms commodity competition. This translates into real performance: shorter total cure times, fewer operator adjustments, and longer storage intervals without yellowing or viscosity drift.
Real-world feedback from partners across medical materials, composites, and color chemistry led our process improvement cycle. Early batches had higher background color and slightly wider boiling ranges—a problem shared by almost every new producer. Over time, after investigating returns and lost orders, we stepped up purification: multiple fractional distillations, actively monitored recoveries, low-metal catalyst cascades, and aggressive wash-downs at every stage. Every process tweak responded to what matters: cure time for adhesives, color for dyes, shelf-life for medical polymers, and ease of paperwork for regulated markets.
It’s tempting to chase the lowest cost by relaxing purity or narrowing test scope. Our operations team built QC protocols around “worst-case” customers—the ones operating highly visible, regulated product lines. That means testing beyond baseline: targeting not just amine and water but residual aromatic and ring-substituted impurity profiles. Every spec adjustment received real-world validation through pilot runs. Returns dropped. Operators stopped reporting random hard spots or color blurring. That’s not just a function of better chemistry, but a system where people fix mistakes and learn across batches.
For specialty dye intermediates, the color endpoint can shift with just a few parts per million of residual base, so our technical reps work directly with user labs, not just sales reps. Advice on storage, handling, and container prep draws from practical experience, not generic manuals. Specialty blends or tweaks—for example, higher dryness or colorless sub-cuts—came from years of fielding odd, challenging orders with stubborn success rates.
We remain deeply involved throughout the usage chain. Post-shipment support covers logistical troubleshooting, rapid replacement for damaged containers, and hands-on guidance for site tank cleaning to prevent cross-contamination. This keeps systems running and contracts on track—a direct reflection of manufacturing depth, not just lab results.
Aromatic amines bring both opportunity and risk. Regulatory compliance in Europe, the US, and increasingly in Asia imposes thresholds on amine use, worker exposure, and emissions. Experience as a producer—not a middleman—means we stay ahead of rule changes, adapt labeling and MSDS content, and invest in containment to protect both operators and end users.
N,N-Diethyl-P-Toluidine presents its own safety profile: moderate toxicity and flammability, with controlled handling through closed-system loading, metered pumping, and vapor abatement. Practical spill response and emergency action form part of operator training. Over the years, as customer audits asked for better tracking, we implemented cradle-to-gate documentation—covering not just drum history but returnable container tracking, staff exposure logs, air quality assurance, and on-site PPE protocols. Downstream users benefit when the supply source delivers clear, honest paperwork and real-world advice in line with the latest restrictions or hazard ratings.
Our investments in in-plant safety, labeling, and operator feedback loops came from learning the regulatory and workplace realities of industries that cannot tolerate downtime or rework due to safety noncompliance. This approach supports both safe worker environments and seamless customer compliance audits.
Global sourcing disruptions and shifting trade landscapes have made reliable supplier relationships essential. Over years of chemical production, we’ve learned the pitfalls of single-source dependency, the importance of secure shipping routes, and the need to plan for changing regulations. Field failures from sub-standard, repackaged, or mis-declared materials have left deep scars on downstream manufacturers.
We built our current logistics networks by prioritizing container integrity, customs documentation, and regular performance benchmarking for hauliers and forwarders. Routine internal training covers risk points: from proper load securing to rapid response for damaged or leaking drums. We track every batch with shipping data, temperature logs, and chain-of-custody records. Customers in specialty applications—from dental resins to technical dyes—gain peace of mind knowing their supply comes straight from the line, not from capricious trading floors.
We take part in collaborative R&D with both suppliers and end users. Our engineering teams partner with equipment sellers and tollers to evolve purification technologies, aiming for both performance and environmental compliance. Years ago, facilities like ours relied on basic vacuum distillation and water-washing. Today, we use fractionation, specialized carbon filters, and continuous monitoring, which lead to lower background color and improved product shelf life.
Joint projects with adhesive producers or dye labs allow us to identify new requirements—low-smell amines for consumer packaging, or ultra-pure intermediates for electronic-grade polymers. Our technical teams keep lab-scale pilot plants running, putting new specs and blends to the test before they hit full production. Every improvement has roots in field issues, not abstract ROI calculations.
Manufacturing aromatic amines poses environmental challenges. Our region enforces strict limits on VOC emissions, water discharge, and hazardous waste. Instead of off-loading risk to subcontractors or disposal outfits, we invested in on-site treatment, fully-closed washing lines, solvent recovery, and reliable flare stacks. These choices came after direct experience—permit violations, air complaints, or water utility discoveries. Adapting operational discipline has turned environmental risk into a management responsibility, not just a compliance cost.
Continuous improvement comes from watching real discharge results, not only lab models. Our teams conduct monthly waste audits, trace byproducts, track residuals, and adjust treatment based on incoming and outgoing load. Customers who require environmental assurances get full documentation, process transparency, and proof that processes back up promises.
Supplying N,N-Diethyl-P-Toluidine means putting daily effort into every link of the chain—from raw material qualification through closed-system transfer all the way to post-delivery technical support. Customers who have come to us from trading houses or spot-buyers tell us the biggest value is predictability: fewer rejections, less end-of-quarter panic, and more control over what actually reaches their line. Each drum is a product of hundreds of discrete, measured decisions. We stand by every batch with full transparency and an open-door policy for audits and customer visits. Our experience as a manufacturer gives us the confidence to deliver real reliability and open the door for innovation at the end-user’s site—not just satisfy a technical data sheet.
The market will always offer shortcuts. Experience in producing, shipping, and supporting N,N-Diethyl-P-Toluidine shows that thorough manufacturing discipline creates real, measurable value that outlasts trends and withstands scrutiny from the world’s most demanding buyers. From our perspective, N,N-Diethyl-P-Toluidine means more than a line on a price list—it’s a reliable tool built on the backbone of hands-on chemical expertise.