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HS Code |
334086 |
| Cas Number | 620-17-7 |
| Molecular Formula | C9H13N |
| Molecular Weight | 135.21 g/mol |
| Iupac Name | 2-methyl-N-ethylaniline |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 219-221 °C |
| Melting Point | -17 °C |
| Density | 0.964 g/cm³ |
| Solubility In Water | Slightly soluble |
| Flash Point | 97 °C (closed cup) |
As an accredited 2-Ethylaminotoluene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-Ethylaminotoluene, 100g, is supplied in a tightly sealed amber glass bottle with hazard labeling and safety instructions printed clearly. |
| Shipping | 2-Ethylaminotoluene is typically shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It should be stored and transported in cool, well-ventilated areas away from sources of ignition, heat, and incompatible substances. Proper labeling and documentation according to local, national, and international transport regulations are required. |
| Storage | 2-Ethylaminotoluene should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from direct sunlight and sources of ignition. Keep away from incompatible substances such as oxidizing agents. Use in a chemical fume hood if necessary. Properly label the container and restrict access to trained personnel only. Store at temperatures recommended by the manufacturer. |
Applications of 2-Ethylaminotoluene in Industrial ManufacturingAs a direct manufacturer, we supply 2-Ethylaminotoluene to global industrial customers engaged in high-value synthesis across the dye, pigment, pharmaceutical intermediate, and agrochemical sectors. The following are key application scenarios currently realized by major downstream users, each reflecting sector-specific process demands and compliance priorities. 1. Synthesis of Azo Dyes for TextilesMajor dye manufacturers use 2-Ethylaminotoluene as a key intermediate when producing bright, durable azo dyes requiring strong bonding to cellulosic and synthetic fibers. Its stable amine structure and methyl ring substituent promote precise diazotization and coupling reactions, supporting colorfast dye formulations for demanding textile finishing lines. Batch scale dyehouses particularly rely on its predictable reactivity for achieving shade consistency in large-volume cotton and polyester runs. Industry compliance standards
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2. Pharmaceutical Intermediate for Antihypertensive AgentsPharmaceutical manufacturers employ this compound as a starting amine in the multi-step synthesis of advanced intermediates, including those used in the production of alpha-adrenergic blockers. The precise methyl and ethylamino functionality allows controlled regioselective reactions, which are critical for subsequent aromatic substitution and side-chain elaboration during GMP-compliant active pharmaceutical ingredient (API) production. Industry compliance standards
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3. Pigment Intermediate for High-Performance CoatingsProducers of automotive and industrial coatings incorporate 2-Ethylaminotoluene for synthesizing pigment molecules with enhanced weather stability and chroma. Its molecular structure supports the creation of nitro- and azo-pigment intermediates used in both solvent-based and water-based pigment dispersions for corrosion-resistant coatings and decorative plastics. Quality control teams value its reactivity consistency, which supports tight finished pigment specifications. Industry compliance standards
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4. Agrochemical Intermediate in Herbicide SynthesisLeading agrochemical firms utilize this intermediate when producing select phenoxyalkyl and phenylurea herbicides. Its ethylaminotoluene backbone is well-suited for constructing molecules that require controlled electron-donating groups, which fine-tune plant selectivity and biological persistence. Plants employing continuous processing appreciate its consistent conversion rates during scale-up for crop protection actives. Industry compliance standards
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Producing 2-Ethylaminotoluene involves clear technical knowledge, a precise process, and decades of hands-on experience with aromatic amines. As a manufacturer, each lot follows a method developed and refined through continuous feedback from real-world users in chemical synthesis laboratories, research centers, and pilot-scale industrial applications.
This aromatic amine, part of the toluidine family, earns ongoing demand in fine chemicals and pharmaceutical intermediates. Chemically known as o-toluidine ethylamine, 2-Ethylaminotoluene (often referenced in literature under its CAS number 5296-60-2) combines the benefits of both toluene-derived and ethylamine-derived compounds. The structure comprises a benzene ring with a methyl group and an ethylamino group at adjacent positions, resulting in both nucleophilic and electrophilic characteristics. That dual nature creates possibilities in synthesis, coupling reactions, dye precursors, and custom intermediates for new molecule development.
Years of manufacturing such compounds taught us to watch for critical reaction steps, especially below 0.1% impurity thresholds that research and pharmaceutical end-users now expect. Trusted facilities rely upon raw material traceability and chromatography equipment staged for accurate fraction separation; these drive reliable outcomes.
Drawing from our experience, specifications reflect not just the published purity but also secondary performance factors. Consistent color, minimal by-product formation, and stability during storage stand at the forefront of quality assurance. For 2-Ethylaminotoluene, most manufacturers claim assay levels of at least 98% by GC. Regular batches from our reactors clock average purities between 98.5% and 99.5%, supporting laboratory and downstream industrial use, including acylation, coupling, or alkylation steps. Liquid at room temperature, the compound runs clear to pale yellow, with a mild amine aroma that signals its integrity compared with off-grade or third-party stock.
Bulk density, flash point, and melting point all receive routine checks to support customers running batch or continuous reactors. Handling advice—based not on legal caution but firsthand process observations—focuses on keeping the material dry and out of sunlight, preventing degradation that can affect yields in sensitive applications. Freshness directly shapes color intensity and conversion rates in follow-up chemistry.
Over the years, end-users sought 2-Ethylaminotoluene for several core activities. In academic and commercial chemistry, its role as a building block for custom ligands, specialty dyes, and pharmaceutical intermediates stands proven. Formulators often turn to this molecule because the ethylamino group increases solubility and broadens downstream modification options compared with plain toluidines or methyl aniline isomers.
Longstanding feedback shows that the ethylamino function offers a more robust site for acylation, creating stable amide bridges required in kinase inhibitors or other advanced medicinal chemistry leads. Dyes and pigments producers trust it in multi-step syntheses for new chromophores—combined with sulfonated aromatic compounds, our batches have driven successful pilot programs at multiple customer sites. The aromatic ring accepts nitration, halogenation, and Friedel-Crafts alkylation with good yields, paving the way for more complex chemical architectures.
Our technical team often collaborates on scaling solutions, leveraging practical knowledge about by-product control. Customizations—such as in-process hydrogenation or selective protection of the amino group—let partners push the molecule into new patent landscapes. From anti-infective API intermediates to ligands in material science, this flexibility drives repeat contracts and long-term development projects.
Any synthetic organic process runs best with reliable raw materials. From the start, our company prioritized eliminating key side products that arise from over-alkylation or ring mis-substitution. N,N-diethylaminotoluene and other positional isomers otherwise slow reactions or cause unpredictable beta testing setbacks for partners further down the value chain.
Manufacturing teams run precise distillations followed by HPLC and gas chromatography every shift. We learned years ago that real-world users see more value in predictable impurity profiles than just a high headline purity. Systematic logs and batch retention samples help customers trace any anomalies back to a specific lot—vital peace of mind for those running multi-kilogram scale-ups or regulatory filings.
2-Ethylaminotoluene presents as a colorless to faint yellow oily liquid under normal room conditions, with a boiling point in the 240–250°C range. These physical traits distinguish it clearly from lower-molecular-weight amines or heavier biphenyl compounds often mistaken for it by less-experienced sources.
Many chemists ask about differences between 2-Ethylaminotoluene and other toluidines or aminotoluenes. From the manufacturer's bench, we see substantive contrasts. The position of the ethylamino group—in the ortho position (adjacent to the methyl group)—matters. This orientation increases reactivity toward electrophilic substitution compared with meta or para isomers, allowing better regioselectivity in certain reaction conditions. Methyl and ethyl substituents modulate electron density, creating more options for derivatization.
Engineers running continuous reactors often report reduced fouling and fewer side reactions compared with basic o-toluidine, especially as the ethylamino group imparts greater solubility in polar and nonpolar solvents. This trait streamlines downstream purification and reduces solvent use—important for compliance and cost controls.
Those transitioning from methylaminotoluene to 2-Ethylaminotoluene often expect identical performance; field experience says otherwise. The ethylamino group supports higher degrees of alkylation during late-stage synthesis, essential for medical chemistry and pigment production. Moreover, shelf-life in sealed, dark storage runs longer than with unsubstituted toluidines.
Long before regulatory paperwork, best practices form in response to near-misses or actual incidents. Years manufacturing aromatic amines underscore the importance of adequate personal protective equipment, good extraction ventilation, and tight spill control—not only for regulatory safety but also to protect final product quality from trace contaminants.
In shipping, we see a marked difference between newly filled drums and those stored poorly. Slight color changes point to oxidation or contamination; transparency and routine sample checks give customers confidence. Direct manufacturing relationships speed up resolution since we control chain-of-custody—buyers get answers faster compared to sourcing from traders or distant brokers.
Shipping conditions also matter. Our team knows which carriers handle aromatic amines with required care, reducing the odds of extended exposure to heat or sunlight. Tight scheduling with trucks and container routes means fresher product upon arrival and fewer headaches for warehouse teams.
Operating modern chemical plants means grappling with evolving environmental stewardship. Decades spent making aminotoluenes highlighted ways to reduce waste, reclaim solvents, and monitor air emissions before regulations demanded it. We've invested in closed-loop filtration for process water and heat recovery systems that reduce both costs and energy use.
Customers now expect not only technical quality, but proof of compliance and green chemistry steps at every stage. Our R&D teams track the European Union’s REACH regulation, US EPA guidelines, and ongoing changes in Asian export controls. Documentation helps partners pass on institutional knowledge, satisfy regulators, and reassure downstream buyers. Indeed, the cumulative expertise accrued through years of direct manufacturing makes safety, regulatory, and sustainability performance more robust than brokers or batch-only processors.
Sourcing raw materials for consistent 2-Ethylaminotoluene production is rarely static. Market pressures in benzene, toluene, and ethylamine supply chains create cost and availability waves. Building strong upstream relationships allows us to adjust purchasing contracts and maintain uninterrupted production. Customers do better when these bumps in the road stay invisible to them.
From practical experience, problems most often arise at the interface between chemical supply and the customer’s production line. Good documentation, proactive communication, and fast double-checking of lot consistency resolve most issues before they impact timelines or yield. Our technical team visits user plants for troubleshooting or process upgrade support; direct insights shorten problem-solving cycles.
Common applications occasionally run up against specialized issues: dye houses sometimes observe unexpected precipitation if solvent ratios deviate, while pharma intermediates may reveal latent impurities during scale-up. Addressing these factors demands both responsive lab analysis and — critically — a willingness to modify procedures on the fly based on production realities rather than lab-scale theory.
Manufacturers who work close to the user gain a different view than distant intermediaries. New requests might emerge as a customized impurity profile, a preferred solvent system, or tighter container cleaning standards. Experience shows willing adaptation beats rigidity; customers have returned time and again for in-person troubleshooting, process optimization, and bespoke packaging.
The trend toward open innovation in the chemicals sector makes these relationships more valuable than ever. Providing 2-Ethylaminotoluene as a mere commodity overlooks opportunities to improve processes and products through feedback loops. We encourage clients to share unexpected findings—good or bad—so we can adjust not just this product’s manufacturing, but sometimes our broader portfolio approach.
Over the years, collaborations with university research labs, global pharmaceutical manufacturers, and fine chemical producers have seeded a culture of shared expertise. Knowledge transfer—especially in organic chemistry routes with subtle substitution patterns—helps end-users push boundaries on synthesis, cost-saving, and environmental improvements.
Recent years brought several process improvements, each driven by persistent customer needs. Improving catalyst recovery allowed for cleaner conversion, dropping trace ruthenium and nickel below the detection limit. Switching purification lines from traditional silica gel to newer composite chromatography columns not only increased throughput but reduced both solvent waste and labor intensity.
Automation has made a real impact. Inline sensors now check amine content, boiling point, and color in real time, flagging drifts immediately to shift engineers and letting batches be requalified or recycled rather than shipped out. This reduces returns and eliminates delayed surprises for customer labs.
Responding to the push for green chemistry, we’ve shifted to eco-friendlier cleaning and neutralization agents, cutting process effluent toxicity. Customer audit teams consistently cite these steps as advantages over brokers or batch-only suppliers. Our internal metrics show each ton now generates 24% less byproduct mass than five years ago.
Researchers and commercial-scale manufacturers alike find value in technical support tied directly to the source. While doing roundtables with polymer additive formulators, our team shared adaptation tips. Changing solvent bases or fine-tuning the percent excess of ethylamine during synthesis helps produce higher-purity yields and tailored reactivity for downstream applications.
Scaling up from milligram R&D samples to multi-kilogram batches requires more than just larger vessels. Engineers and chemists need consistency in melting and boiling points, viscosity, and impurity load—especially for reactions where side products can poison catalysts or block filters. We routinely provide close-lot sampling for those moving from proof-of-concept to their first pilot plant trials.
Most who work with custom aromatic amines come to appreciate that real-world process robustness is earned, not claimed. Customer success stories often center on how a single variable—like container type or heat profile—can make or break production. With each technology transfer or process scale discussion, we feed lessons learned back into our SOPs, driving continual improvement.
It’s easy to claim technical compliance or match published purity figures; experience in the field reveals subtle but important differences. Consistent lot traceability, willingness to support technical discussions, and on-time logistics separate long-established manufacturers from resellers. Over the years, we’ve taken over supply to customers left frustrated by supply lags, incomplete documentation, or off-profile material.
User satisfaction depends on more than the molecule itself: it arises from deep product know-how, responsiveness to customer technical questions, and anticipation of downstream hurdles. The direct relationship gives us freedom to adapt purification, packaging, or even the specification envelope at the customer’s request—without the delays inherent to third-party sourcing. In partnerships where repeated success matters, the difference becomes obvious.
For an experienced manufacturer, batch-by-batch care and continuous technology refresh takes resources—and it’s worth it. Customers report smoother integration during scale-up, fewer unexpected impurities, tighter documentation, and a real sense that their process matters to us as more than a line item. Such collaboration continues to shape the evolution of 2-Ethylaminotoluene production, and keeps both supplier and customer at the front edge of chemistry innovation.