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HS Code |
988878 |
| Chemical Name | 4-[(2-Chloroethyl)Ethylamino]-Benzaldehyde |
| Molecular Formula | C11H14ClNO |
| Molecular Weight | 211.69 g/mol |
| Cas Number | 22115-72-0 |
| Appearance | Pale yellow to brown crystalline solid |
| Melting Point | 56-58°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Purity | Typically ≥98% |
| Storage Conditions | Keep in a cool, dry, well-ventilated place |
| Synonyms | N-Ethyl-N-(2-chloroethyl)-4-formylaniline |
As an accredited 4-[(2-Chloroethyl)Ethylamino]-Benzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams, sealed with a screw cap, labeled with chemical name, hazard symbols, and handling instructions. |
| Shipping | 4-[(2-Chloroethyl)Ethylamino]-Benzaldehyde is shipped in compliance with chemical safety standards. It is securely packaged in airtight, corrosion-resistant containers, labeled with hazard information. The shipment is handled by trained personnel, following all relevant regulations for hazardous materials, including documentation and transport restrictions to ensure safe delivery and environmental protection. |
| Storage | Store 4-[(2-Chloroethyl)ethylamino]-benzaldehyde in a tightly sealed container, protected from light, moisture, and incompatible substances. Keep at room temperature, in a cool, dry, and well-ventilated area away from oxidizing agents and acids. Ensure proper labeling and use secondary containment to prevent leaks. Follow local regulations and use appropriate personal protective equipment when handling or accessing the storage area. |
Applications of 4-[(2-Chloroethyl)Ethylamino]-Benzaldehyde in Industrial ManufacturingAs an original manufacturer, we supply 4-[(2-Chloroethyl)Ethylamino]-Benzaldehyde specifically for advanced industrial platforms requiring high standards of chemical reactivity and purity. Our production capacity allows integration into multiple downstream sectors where tailored compliance, process consistency, and predictable output are essential for mass production. 1. Pharmaceutical Intermediate for Antineoplastic AgentsPharmaceutical manufacturers use this molecule as a key intermediate to synthesize nitrogen mustard derivatives, especially in the development of alkylating antineoplastic drugs. In commercial active pharmaceutical ingredient (API) synthesis lines, chemists employ it during several stages of the multistep process, leveraging its aldehyde group for targeted condensation and its chloroethyl segment for functional modification. The end application focuses largely on oncology therapeutic products, where strict control over impurity profiles and batch reproducibility is mandatory to comply with regulatory filings. Industry compliance standards
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2. Precursor in Fine Chemical Synthesis for Dyes & PigmentsFine chemical producers incorporate this functionalized benzaldehyde to produce specialty aromatic compounds used in high-performance dyes and pigment manufacturing. The molecule's bifunctional structure supports targeted transformations—such as azo coupling or further halogenation—enabling synthesis of vivid colorants with specific lightfastness or solubility profiles demanded for industrial textile and plastics coloration. Industry compliance standards
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3. Building Block for Agrochemical Active IngredientsAgrochemical companies integrate this aldehyde-based compound in the advanced synthesis of certain pre-emergence and selective herbicides, as its chlorinated backbone allows for derivatization into biologically active molecules targeting specific weed species. Consistent batch-to-batch quality is vital as regulatory bodies strictly monitor precursor provenance and residual impurity limits in the final actives. Industry compliance standards
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4. Intermediate for Specialty PolymersProducers of functional polymers employ this compound for introducing reactive benzaldehyde groups into polymer chains, facilitating crosslinking and property modification in specialty resins. This approach offers enhanced thermal properties or chemical resistance required by performance-driven sectors such as electronics encapsulation and high-durability coatings. Industry compliance standards
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We have manufactured 4-[(2-chloroethyl)ethylamino]-benzaldehyde for years, watching industries rely on it through changing research directions and a market that does not pause for inconsistent quality. As a chemical plant with direct hands-on experience, we do more than pour reactants and check off boxes—each batch reflects the lessons learned when things worked and, more importantly, when they occasionally didn’t.
Chemistry laboratories and pharmaceutical intermediates producers turn to this molecule for its predictable reactivity. Not every compound that looks similar on paper handles as smoothly on the line or meets strict tolerance in yield and purity. In our work, the difference emerges from the practical details of how it holds up through longer syntheses and under heavier demand. This isn’t just another substituted benzaldehyde; the 4-[(2-chloroethyl)ethylamino] side chain gives it specific behavior, especially in alkylation reactions and building up advanced intermediates.
Manufacturing starts with the structure. The 4-position on the benzaldehyde ring offers a key site for functionalization. Incorporating both an ethylamino and a 2-chloroethyl group sets this molecule apart from simpler aldehydes that chemists have tried over the decades. Our reactors see materials that need to hold their composure under temperature and subtle changes in pressure. The distinctive substitution at the para position achieves just that, minimizing side reactions and offering a more straightforward progression in multistep synthesis plans.
Speaking from hard-earned experience, purity specifications make all the difference downstream. Even minor contamination from structurally similar derivatives alters the progress of more complex syntheses. We have tuned our crystallization processes, monitored residual water content, and controlled for stabilizer presence with vigilance. Our customers benefit from these stringent checks, not abstract “quality assurance” claims, but tangible avoidance of extra purification steps and wasted material.
We produce 4-[(2-chloroethyl)ethylamino]-benzaldehyde in batches that typically meet a purity specification exceeding 98%. This isn’t a random number. Less than that, and you may run into trouble if you are coupling acids and aldehydes with tight requirements for byproduct removal. We work with melting points measured at standard atmospheric conditions, ensuring they confirm lot consistency. Moisture content, controlled below 0.5%, makes a difference in handling: sticky, hygroscopic samples slow everything down. Our experience tells us fresh material retains a faint but distinctive aldehyde odor—an indicator you are working with a real aldehyde, not an overprocessed substitute.
Over years in the trenches, we have seen how packaging plays a role. We use lined drums and ensure nitrogen blanketing for long-distance shipment. One spill or damp environment can turn a high-spec batch into a sticky mess, reducing yield and reliability. Frequent feedback from downstream users keeps us alert to necessary tweaks in storage and transport, and we keep validating new container materials after every change in the market.
Much as catalogs suggest otherwise, the real differences emerge during scale-up. Paper technical data does not always guarantee that the material will scale past grams to multi-kilogram or metric ton amounts. We have optimized our synthetic process to minimize formation of an undesirable bis-chloroethyl byproduct—a common impurity among less controlled syntheses that can throw off catalysts and poison reaction mixtures during hydrogenation or nucleophilic substitution.
The biggest difference from other benzaldehydes appears during subsequent steps. In our experience with custom synthesis and contract manufacturing, clients often present us with routes that use similar substrates. Direct analogues with methyl or isopropyl groups instead of the 2-chloroethyl chain tend to be less versatile in follow-on N-alkylation or cyclization, closing the door on several classes of heterocycles. Our variant delivers more pathways, saves time in multi-step organic synthesis, and matches project timelines that face unexpected pivots.
Most of our customers use 4-[(2-chloroethyl)ethylamino]-benzaldehyde as an intermediate. We see it most commonly funneled into active pharmaceutical ingredient (API) research and custom fine chemicals manufacturing. The presence of the chloroethyl moiety brings synergies in the preparation of nitrogen mustards, important in cancer therapy research and, with certain modifications, in agricultural control agents. Other benzaldehydes simply do not serve as useful springboards for these applications, either due to lower reactivity or problematic byproduct profiles.
Our production teams frequently collaborate with research groups working on analogues designed for targeted therapies. We provide small- to mid-scale quantities with monitored timelines, knowing they cannot spend weeks troubleshooting starting materials. Not only do we support projects trying to replicate classic routes from the literature—our batches have served in process modifications for faster or more environmentally-friendly syntheses.
In specialty material science, innovators take advantage of this reagent for the construction of functionalized polymers, where the controlled introduction of chloro groups paves the way to new cross-linking patterns. Our real-world experience tells us most attempts to substitute with cheaper variants fail, either through incomplete reactions or inability to match desired physical properties. End-users often share feedback with us, and we feed those insights back into the production cycle.
A key challenge we've solved involves heat management. Reactions using 4-[(2-chloroethyl)ethylamino]-benzaldehyde require careful temperature modulation to avoid runaway conditions, especially during large-scale alkylations. We designed jacketed reactors and implemented consistent agitation, cutting down on hot spots that lead to byproduct formation and lowering the risk of off-gassing anything unnecessary. This hands-on approach results in reproducible yields and tighter process controls for our clients.
Looking at the competition, we notice they sometimes ship material still containing legacy process impurities—unreacted haloalkylamines or, worse, polymers that gum up filter beds. Over time, we’ve learned to strip out those problem-makers through a mix of column chromatography and careful pH adjustments. It may seem small, but stories from process engineers confirm that a little extra effort up front saves hours, or sometimes days, downstream.
Part of our commitment goes into safety and documentation. We provide transparent, batch-specific impurity profiles—not just a boilerplate certificate. Our QA teams maintain historical data for each lot, enabling full traceability. This isn’t an optional service; regulatory customers, especially in the pharmaceutical segment, expect to see a clean audit trail. Proper labeling, serial tracking, and compliance documentation help avoid costly setbacks if an inspector requests proof of origins or process controls.
We run extensive hazard assessments, knowing that chloroethyl groups carry risks during handling. We instruct every new team member in correct PPE use and maintain local exhaust systems near workstations. It is not about meeting a checklist; these are real people relying on the protocols put in place. Customers working with hazardous intermediates need this kind of upstream diligence.
Some of our biggest process upgrades have grown out of direct user feedback. A pharmaceutical customer once flagged accelerated yellowing in stored aldehyde over six months. Instead of dismissing it as just another shelf life warning, we dug in and discovered a stabilizer carryover issue—a fixable detail. By switching purification vendors and retesting shelf stability, we cut discoloration nearly in half, reducing wastage at every major client.
We approach each report as an opportunity to boost our batch performance. If an end-user points out solubility issues in a new solvent, we retest the material under those conditions, then update our technical support documentation. Research chemists and process engineers form the backbone of our improvement cycle—they know the pain points and we use their experience to fine-tune production parameters, packaging, and logistics.
Years of up-and-down markets have underscored the need for cost predictability without shortcuts. We hedge crucial starting materials and secure partner relationships with key upstream manufacturers, enabling us to avoid the monthly volatility that plagues more lightly-capitalized suppliers. Customers who partner with us directly have repeatedly expressed relief at not being forced into last-minute re-scoping due to price swings.
We also face questions on greener chemistry and route optimization. Manufacturing 4-[(2-chloroethyl)ethylamino]-benzaldehyde doesn’t yet feature the lowest-carbon options—it’s an industry-wide challenge rooted in olefin and amine feedstock production. We collaborate on pilot projects to recycle solvents and recover energy from exothermic reaction stages, and push for less wasteful purification campaigns. The smallest improvement—yield, waste minimization, solvent recycling—compounds over hundreds of production cycles.
Clients weighing options often ask how our 4-[(2-chloroethyl)ethylamino]-benzaldehyde differs from off-catalog or fast-shipped alternatives. The truth plays out beyond a price tag. Consistency in aldehyde content, accurate structural assignment, and the absence of trace, undetectable isomers—the difference is measured in avoided downtime, not just line items on a quote. Material from third-party traders sometimes comes with contamination or contradictory analysis sheets.
Direct sourcing with a factory experienced in the quirks of this particular molecule pays off when you hit a snag. We share detailed chromatographic and scalar NMR data matched to each lot, so you don’t discover surprises after solvent evaporation or crystallization. If a route adjustment is needed mid-stream, we can collaborate on testing and batch modifications quickly, ensuring realistic timelines and goals.
Advances in synthetic chemistry keep pushing for more flexibility. Even while machine learning and automated reactors promise to change the landscape, the real bottleneck still lies in access to trusted building blocks with minimal fuss in documentation or downstream reactivity. We keep investing in method improvement and workforce training so our 4-[(2-chloroethyl)ethylamino]-benzaldehyde meets tomorrow’s standards as well as today’s.
Our long-term partners continue to shape how we approach both scale and customization. As demand for pharmaceutical-grade intermediates rises, and regulatory pressures mount, we treat each discussion with end-users as a step toward not just meeting, but anticipating, the real-world headaches of synthetic chemistry. By keeping close to the daily grind of actual chemists—those on the bench, in the pilot plant, or managing final API manufacturing—we ensure our product stays relevant, dependable, and responsive to shifting needs.
Every lot of 4-[(2-chloroethyl)ethylamino]-benzaldehyde that leaves our facility reflects a continuous cycle of improvement forged in direct response to industry need. Our history in chemical production has taught us that reliability counts for more than buzzwords or theoretical performance. Each order becomes a partnership, connecting the production floor with laboratory and industrial applications across the globe.
Work with manufacturers willing to share their process, document every change, and act on feedback—those values keep the field moving forward. In our shop, we keep refining our 4-[(2-chloroethyl)ethylamino]-benzaldehyde, pushing for cleaner, safer, and more adaptable outputs, so every user—from academic researcher to contract pharma facility—can spend more energy creating value and less time dealing with unreliable raw materials.