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HS Code |
636962 |
| Cas Number | 142-42-7 |
| Molecular Formula | C6H13N |
| Molecular Weight | 99.17 g/mol |
| Iupac Name | N-ethyl-2-methylprop-2-en-1-amine |
| Synonyms | N-Ethyl-2-methylallylamine |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 101-104°C |
| Density | 0.782 g/cm3 at 25°C |
| Flash Point | 17°C (Closed cup) |
| Pubchem Id | 77400 |
| Smiles | CCNCC(C)=C |
| Solubility In Water | Miscible |
| Refractive Index | 1.429 |
As an accredited N-Ethylmethallylamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 250 mL amber glass bottle with tamper-evident cap, labeled “N-Ethylmethallylamine.” Includes hazard symbols and lot number. |
| Shipping | N-Ethylmethallylamine should be shipped in tightly sealed, clearly labeled containers, stored in a cool, dry place, and protected from light, moisture, and incompatible substances. Ensure compliance with local, national, and international regulations during transit. Appropriate hazard labeling and documentation are required, and carriers must be informed of the chemical’s flammable and irritant properties. |
| Storage | N-Ethylmethallylamine should be stored in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizers and acids. Keep the container tightly closed when not in use and store in a designated chemical storage cabinet. Protect from moisture and direct sunlight. Ensure appropriate labeling and follow all local regulations for chemical storage. |
Applications of N-Ethylmethallylamine in Industrial ManufacturingN-Ethylmethallylamine serves a critical function in several specialized chemical production sectors. We support customer innovation by providing consistent, high-purity supply, technical integration guidance, and authentic quality assurance. Below, we detail the primary industrial segments where this amine is essential, focusing on compliance, formulation, release point in manufacturing lines, and representative end products. 1. Synthesis of Polymeric Flocculants for Water TreatmentOur customers in the water treatment industry utilize N-Ethylmethallylamine as a reactive monomer for the synthesis of polyacrylamide-based flocculants. The unique aminoalkyl structure provides enhanced cationicity to the resulting polymers, improving performance in removing suspended solids from municipal and industrial waste streams. Manufacturers blend it into the acrylamide monomer mix at tightly controlled ratios to regulate molecular weight and charge density, directly impacting final separation performance. Industry compliance standards
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2. Intermediate for Active Pharmaceutical Ingredient (API) SynthesisPharmaceutical manufacturers employ N-Ethylmethallylamine as a key intermediate for the alkylation and amination steps in small-molecule drug synthesis. The amine group offers selectivity for catalytic coupling reactions, while the branched structure enables subsequent side-chain functionalization. Strict batch traceability and impurity controls are essential to meet regulatory requirements for human drug production. Industry compliance standards
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3. Epoxy Resin Modifier for Coatings and AdhesivesN-Ethylmethallylamine enables formulators to modify epoxy resin systems, imparting chemical resistance and flexibility to coatings and adhesive products. Its incorporation alters the curing kinetics and reduces brittleness in final cured films. Producers must balance the amine quantity with base epoxy resin and hardener, customizing for end-use—such as protective coatings for industrial floors or specialty adhesives for electronics assembly. Industry compliance standards
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4. Quaternary Ammonium Compound Precursor for Surfactant ManufacturingSurfactant producers utilize N-Ethylmethallylamine as a primary precursor in synthesizing quaternary ammonium salts. The methallyl side-chain provides tailored hydrophobic-lipophilic balance in final surfactant molecules, increasing detergency or antistatic effects according to customer end use. The production process uses this amine in transalkylation or quaternization reactions under tightly monitored conditions to control byproducts relevant for regulatory and quality audits. Industry compliance standards
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5. Corrosion Inhibitor Synthesis for Oilfield ApplicationsN-Ethylmethallylamine functions as a specialty intermediate for the production of oilfield corrosion inhibitor bases. Compounders react it with fatty acids or alkyldicarboxylic acids to produce amide or imidazoline structures, offering effective surface adsorption and water solubility control. The design enables protection of metal surfaces—including pipelines and drilling equipment—under harsh operational environments. Industry compliance standards
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6. Monomer for Functional Polymeric MembranesN-Ethylmethallylamine acts as a functional monomer to introduce ion-exchange capabilities in specialty polymeric membranes. These membranes support a range of industrial separations, from gas purification to desalination. Polymer engineers select the amine content to balance transport selectivity and permeability, thereby optimizing performance for demanding solid–liquid or gas–liquid separation tasks. Industry compliance standards
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Decades of practical manufacturing have shown that even minor adjustments in a chemical's structure can drive genuine progress in downstream synthesis. N-Ethylmethallylamine stands as a clear example. A specialty amine, it blends the distinctive reactivity of a methallyl group with the versatile ethyl chain. This single molecule, produced in facilities committed to process cleanliness and traceability, plays a role in numerous industries but is often overlooked in favor of broader commodity amines. Our process for N-Ethylmethallylamine prioritizes purity and consistent lot-to-lot color, because too many downstream users have faced headaches from darkened or off-odor batches that complicate reaction control. Years of production feedback have taught us that subtle production variables—stirring speeds, feed purity, nitrogen blanket control—can shift a batch’s usability. Our lines are controlled tightly, with regular feedback loops and chromatographic vetting, to satisfy our partners in demanding applications.
Understanding the structure sheds light on where this compound fits compared to other amines. The ethyl group on the nitrogen provides a reliable handle for selectivity during quaternization or alkylation steps. The methallyl piece introduces an unsaturated backbone, bringing in the possibility of addition, polymerization, or crosslinking chemistry. This combination opens up reactivity windows not available to simple alkylamines or to classic diallylamines. For formulators aiming to control conversion rates or graftability, N-Ethylmethallylamine offers a unique middle ground—it’s more reactive than N-alkyl monoamines, less prone to uncontrolled side reactions than N,N-diallyl analogues.
As a manufacturer, we maintain its chemical stability all the way from the reactor to the filling line. Storage and transport conditions are controlled with dryness in mind, since both the amine’s base strength and the unsaturation need to stay uncompromised for high-yield uses. Our internal studies show that even minor tramp moisture, or trace peroxides, can raise the odds of polymer formation during storage—costly issues for end-users in both coatings and synthesis sectors. Experience has forced us to go beyond standard compliance and set our water and peroxide limits below what many others consider acceptable.
Coatings formulators often turn to this amine for the unique blend of surface-activity and chemical reactivity. It works well as a building block for specialty polymers, especially when hydrophobicity and controlled crosslinking are valuable. We supply firms that blend it into epoxy curing agents, seeing the impact directly in faster cure times and better chemical resistance for high-performance floors. Technical staff from customers in adhesive and sealant production routinely confirm that standard monoamines, like ethylamine or propylamine, cannot replicate the balance of flexibility and hardness that N-Ethylmethallylamine-modified resins achieve.
Synthesists in pharmaceuticals and agrochemicals tend to choose this molecule for its mild nucleophilicity. It enables clean N-alkylation steps, often without the overalkylation or side reactions that can plague more basic amines. The methallyl group’s double bond proves useful for further functionalization—hydroboration, bromination, and catalytic additions. In pilot-lab settings, especially in drug intermediate synthesis, this difference has allowed chemists to streamline their steps, cutting down the purification burden seen with less-specialized amines. A client once described shifting from a generic methylamine to our product as the key move in clarifying a reaction, because unwanted dimers and overalkylated byproducts dropped out almost entirely.
Laboratory specs on paper rarely tell the whole story of a fine amine’s performance in the field. Purity as measured by GC or NMR gives part of the picture, but downside risk often emerges from trace aldehydes or heavy metals that might lurk below standard detection limits. Years ago, a single contaminated batch of incoming feedstock almost forced a batch recall at a customer’s epoxy shop. Since then, we set tighter incoming QC on our own raw materials, raising our scrutiny above market minimums for both metal and halide content. These screens catch the risks before packaging—protecting customers from reworking expensive resin lots down the line.
Color and aroma intensity also give early warning. We have found that the faintest yellow tint, often disregarded, correlates with background polymerization activity or oxygen contamination. Long-term field testing on hundreds of commercial lots showed us that controlling reaction pressure and temperature in our own reactors, within a narrow range, directly affects the clarity and shelf life our clients value.
Continuous improvement shapes our N-Ethylmethallylamine line. Process observations, shared by client teams, help us tweak purification and drying steps, so the molecule’s reactivity doesn’t get compromised along the value chain. Batch records document not just input and output data but every deviation handled—whether it’s an abnormally slow phase split or a subtle shift in product pH. We catch these issues at source to avoid surprise during customer use.
Feedback from coatings and synthesis labs pushed us to focus on drum and IBC linings. Some manufacturers still fill into bare-metal containers, but we moved to specialty-lined packaging when users started seeing off-odors from oxidized residue. Post-shipment monitoring, including periodic re-analysis of retained samples, means that any field complaint leads to quick root-cause tracing—nipping recurring issues before they reach critical scale. This vigilance, grown from years of working directly with users, increases both our reliability and the confidence customers have in using the amine for high-value applications.
Over the decades, side-by-side comparisons distinguished N-Ethylmethallylamine from analogues like N-Methylmethallylamine or standard linear alkylamines. Unlike its methyl counterpart, the ethyl variant reacts more gently, enabling reaction rate control essential for tuned end-properties in polymers and specialty chemicals. The added steric hindrance of the ethyl group discourages excessive side reactions, which proves vital in pharmaceutical syntheses and controlled polymerizations. Where cost-sensitive buyers lean toward bulk suppliers offering looser specs, many of our longstanding partners stick with us for this reason—they know shortcuts at this molecular level can cause expensive headaches down the line.
N,N-diallylamines look similar on a first glance, but practical differences remain obvious to process chemists. Diallyl derivatives show much higher reactivity, increasing the risk of runaway polymerizations or crosslink density beyond a usable range. Only N-Ethylmethallylamine walks the line between flexibility and function, letting formulators choose physical property targets without sacrificing processing control. Over years of in-application comparisons, only a handful of alternative molecules gave similar results, but either introduced new regulatory concerns or lacked the supply stability customers demanded. This balance remains a key reason we have seen repeat calls from specialty sealant, floor coating, and precision organic synthesis buyers year after year.
Producing N-Ethylmethallylamine responsibly requires staying ahead in both compliance and supply chain transparency. Our QA systems don't merely tick boxes for routine regulatory filings—they alert us immediately if a process deviation could compromise data, and our traceability links every drum back to its reactor shift and feedstock lot. Since regional regulations in Europe, North America, and Asia all have subtle differences in allowable impurities and handling requirements for amines with unsaturation, we maintain dialogue with our customers’ compliance departments. When downstream products need documentation for REACH or TSCA, our supply documentation arrives ready—a detail valued by any buyer who’s experienced delays from a noncompliant or incomplete supplier package.
We don’t claim perfection, but we pursue continual improvement in both analytic methods and process hygiene. Internal labs run both conventional and advanced screens, making sure our lots will not raise flags in even the toughest external audits. Maintaining compliance sometimes requires quick pivoting—from expanding heavy metal screens to improving batch isolation technique. Every year, this approach saves both us and our customers costly, time-consuming trouble later in their product life cycles.
Problems in chemical sourcing often stem from inadequate technical dialogue between end-users and manufacturers. Over the years, we’ve learned that the fastest way to prevent bottlenecks or product failures is to involve our technical team early with our customers’ development teams. Whether designing a curing system, developing a new polymer, or exploring a novel pharmaceutical intermediate, chemists and engineers benefit from direct and open communication with producers.
Regular field visits and customer process audits have shown that the best-performing batches result from interface—clients adjust their mixing, dosing, or downstream conditions, while we refine our drying or filtration to match empirical needs. These small collaborations have led to big cost and performance wins. Issues like micro-contamination, mistaken drum selection, or residual solvent traces became rare after building these face-to-face partnerships. Instead of waiting for specification complaints, we work proactively to solve challenges before they impact batch or campaign scale-up.
One recurring challenge for users arises in scale-up from lab to plant. Small-scale syntheses often tolerate trace impurities or small inconsistencies that blow up during commercial runs. After supporting dozens of transition projects, we now monitor not only specification metrics, but also performance metrics defined by downstream users: cure time, conversion efficiency, viscosity, or color hold. This hands-on, real-world feedback has taught us that a specification sheet cannot replace direct data sharing and partnership as molecules move from production to application.
As demand grows for advanced materials and cleaner chemical processes, our production model adapts. We invest in minimizing fugitive emissions, handling energy management, and keeping occupational exposures well below regulatory requirements. New monitoring tools, including higher-resolution analytical methods and in-process controls, help us catch inconsistencies at source.
Some clients now seek even higher levels of purity and documentation, driven by tighter product safety standards and growing consumer scrutiny. To serve this, we increased our trace VOC analysis, moving well beyond routine loss-on-drying or basic GC checks. Customers integrating the amine into medical or food-contact polymers can review full batch data without chasing multiple suppliers or facing data gaps.
As more companies strive for proprietary differentiation in coating, adhesive, or pharmaceutical markets, molecular building blocks like N-Ethylmethallylamine become critical. Our advantage as a direct manufacturer—rooted in long-term operating experience and proven feedback loops—enables us to deliver this amine with a unique blend of reliability, consistency, and responsive support. We share technical process data and adapt our product’s handling, purity, and form of supply to match the reality of applied chemistry.
We judge our success by what our partners make, not just by the specs we list. The trust gained through technical transparency and shared troubleshooting moves us beyond supplier status—we become part of our clients’ value creation stories. With supply chains evolving, regulatory scrutiny rising, and performance needs sharpening every year, choosing the right source for N-Ethylmethallylamine—and understanding what sets one supplier apart—remains fundamental. Lessons learned in the plant and lab never get old; they shape the standards we keep raising for every new lot we ship.