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HS Code |
245728 |
| ProductName | Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate |
| MolecularFormula | C18H19Cl2NO2 |
| MolecularWeight | 352.26 g/mol |
| CASNumber | 65141-46-0 |
| Appearance | White to off-white solid |
| Purity | ≥98% |
| Solubility | Soluble in organic solvents such as ethanol, chloroform, and DMSO |
| StorageConditions | Store at 2-8°C, keep container tightly closed |
| SMILES | CCOC(=O)C(C)N(Cc1ccccc1)C2=CC(Cl)=C(Cl)C=C2 |
| IUPACName | ethyl 2-[(3,4-dichlorophenyl)(phenylmethyl)amino]propanoate |
| Synonyms | Ethyl (Dl)-2-[(3,4-dichlorophenyl)(phenylmethyl)amino]propanoate |
| HazardStatements | May cause skin and eye irritation |
As an accredited Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 100g white, tightly sealed HDPE bottle labeled “Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate, 98%,” with hazard and handling warnings. |
| Shipping | **Shipping Description:** Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-DL-alaninate is shipped in tightly sealed containers to prevent moisture and contamination. It is transported according to standard chemical safety regulations, with labels indicating hazardous material where applicable. The package should be handled with care, stored in a cool, dry place, and kept away from incompatible substances. |
| Storage | Store Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the container clearly labeled and protected from moisture. Use proper personal protective equipment when handling, and follow all relevant regulations for storage of organic chemicals. |
Applications of Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate in Industrial ManufacturingEthyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate serves dedicated roles in select high-value chemical and pharmaceutical manufacturing chains. As a producer, we work directly with formulating, process integration, and compliance requirements to support efficient and quality-driven downstream production. The sections below outline confirmed industrial applications by segment, complete with relevant standards, usage ratios, process pathways, and real-world finished products. 1. Agrochemical Intermediate for Herbicide FormulationManufacturers utilize this compound as a key intermediate in the synthesis of advanced selective herbicides for pre-emergence and post-emergence use. Its dichlorinated aromatic structure contributes to target-specific bioactivity once further derivatized. Production relies on precise upstream purity, ensuring consistent performance through scale-up. Operations require rigorous chemical handling, in-line QC, and subsequent transformation under controlled reaction conditions. Industry compliance standards
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2. Pharmaceutical Intermediate for Chiral Drug SynthesisAPI producers implement this material as a protected amino acid derivative in asymmetric synthesis for various chiral pharmaceuticals. Its structural core enables key bond formations in antagonists or inhibitors targeting therapeutic enzymes. Integration depends on GMP-grade sourcing and pharmaceutical traceability from our batch documentation. Synthesis steps adapt to required chiral purity, supporting controlled environments in pilot or full-scale API manufacture. Industry compliance standards
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3. Fine Chemical Synthesis of Specialty PolymersProducers of specialty polymers engage this compound as a functional monomer precursor, building in custom dichloroaryl features for advanced polymer backbones. Its controlled reactivity fits high-temperature, step-growth, or chain-growth polymerization schemes. Tight process and storage parameters maintain monomer integrity, with adjustments for downstream co-monomer compatibility and branching requirements. Industry compliance standards
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4. Custom Synthesis for Medicinal Chemistry ResearchContract research organizations and pharmaceutical R&D divisions request this alaninate derivative for custom synthesis of small molecule libraries used in lead optimization studies. Its structural elements support structure-activity relationship investigations and scaffold hopping in early drug discovery. Projects require tightly specified purity, trace impurity profiles, and secure documentation against project code or synthetic target. Industry compliance standards
Typical usage ratio
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In specialty chemical manufacturing, few compounds stand out like Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate. Those who spend their careers synthesizing and improving complex molecules know just how much care and expertise this product demands. Years of consistent lab practice have shaped our approach to each step, from sourcing raw starting materials to fine-tuning process parameters. We take pride in the direct connection between the choices made on the factory floor and the reliability of the final material reaching the customer's door.
This compound—sometimes recognized within agricultural chemistry and pharmaceutical research for its intermediate properties—didn’t just enter the market by accident. The long chemical name says a lot. Benzyl and dichlorophenyl groups offer reactivity that plain ester analogs can't deliver. The alaninate ester function tunes the molecular backbone for application in advanced synthesis. Every time we manufacture a new batch, we monitor the distinct fingerprint of the target structure through analytical methods like HPLC, NMR, and mass spectrometry. Each result secures confidence in the repeatability scientists count on when they pull a new drum off the shelf.
Manufacturing this compound at production scale involves more than mixing and stirring. We calibrate reactor temperature profiles to handle the sensitive esterification step and monitor the precise addition of benzylating agents. The dichlorophenyl group, prone to side reactions if managed poorly, gets specific attention from our technical team. Overhead distillation systems, in-line filtration, and inert gas blankets play essential roles in daily operations. Where some see a string of apparatus, we see decades of refinement and improvement.
Quality comes not just from clean glassware or high-purity solvents, but from the people running the process. Our team measures every result—and mistakes on the bench are logged, reviewed, and learned from as a matter of culture. Supplying consistent material over many years builds trust with end users who rely on this compound in applications from crop protection to laboratory-scale medicinal chemistry.
Every kilogram that leaves our warehouse must conform to specifications we have tightened over years of iterative improvement. Moisture content, residual solvent levels, and assay purity (often exceeding 98 percent) set the baseline QC. We don’t offer multiple “grades.” Anything short of this benchmark doesn’t go into a shipment. Years ago, we might have accepted a little more variance batch to batch; feedback from the field taught us otherwise. Scientists developing scalable syntheses or screening bioactivity expect consistent performance.
Physical form makes a difference in day-to-day handling. Our regular product comes as a solid, often with a slightly off-white appearance depending on trace impurities from upstream synthesis steps. Particle size distribution affects not just dispensing accuracy, but also downstream reaction rates and solubility. Through repeated trial, we’ve learned to match the physical properties most researchers prefer, taking care to avoid product that cakes or clumps at typical humidity ranges.
Every data sheet references traditional analytical values—melting point, spectral data, elemental analysis. Back in the lab, we give as much weight to simple, hands-on checks: looks, pours, dissolves with expected vigor, and passes through a sieve without fuss. Sometimes we catch outliers that wouldn’t register in the numbers alone, and this attention to practicality carries as much value as the best instrument readout.
From years spent fielding requests and conversations with synthetic chemists, we know this molecule rarely sits in a warehouse long. Customers typically purchase it to serve as a building block in advanced chemical transformation, often for the discovery phase in agriculture or pharma. The ester group allows for controlled releases, or downstream hydrolysis when required, giving synthetic flexibility rarely matched by related options.
A few groups leverage the dichlorophenyl motif to introduce robust electron-withdrawing functionality onto aromatic frameworks. The same backbone chemistry that drives pesticide research also finds application in tuning biological activity for new lead candidates in early-phase pharmaceutical screening. Many client formulations remain proprietary, but the technical teams who call us for follow-up supply often share enough detail to keep us mindful of practical challenges: shelf stability, reactivity in key transformations, and batch-to-batch physical properties that impact reaction yields.
Our role doesn’t end with a purchase order. Requests for custom packaging, accelerated testing under specific humidity, or tweaks to particle size often reach our door. We treat every request as a signal—evidence for shifting industry practice or evolving scientific discovery. Making room for these conversations increases product value far beyond what lab inventory sheets can capture.
Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate differs from plainer alanine esters in several practical ways. The dichlorophenyl ring introduces substantial hydrophobicity and electronic effects, directly influencing behavior in both synthesis and final formulations. The benzyl group affords another site for further functionalization, giving chemists latitude to build more complex molecules from a single precursor. Standard alaninate esters tend to offer limited reactivity or stability, and often don’t support the breadth of transformations possible with this substituted variant.
Our plant has trialed similar molecules with slightly different aromatic substitution patterns. Minor changes in the phenyl groups—say, exchanging dichloro for difluoro, or moving the benzyl off by a carbon—produce clear differences in solubility, reactivity, and real-world handling ease. Only through years of repetitive pilot and production-scale runs have we mapped which variants deliver what researchers most need: a combination of shelf-stability, reliable conversion in synthesis, and predictability irrespective of weather, shipping time, or storage conditions.
Market feedback confirms what we see in-house. Alternative products lacking the dual aromatic substitution sometimes fail in key steps or introduce unpredictability in batch output. Feedback from one agricultural startup brought our attention to issues of hydrolytic breakdown under humid storage conditions—problems we traced to less robust molecule design in competitors’ analogs. Our plant engineers adjusted both process and packaging to deliver a version that retains integrity across seasons and between continents.
Last year, after demand surged for derivatives designed for slow-release formulations in controlled environments, we doubled down on monitoring for byproduct formation specific to this structure. Now, we regularly compare our own in-process data to third-party analytical norms, always on the lookout for outliers that could signal new challenges. By keeping close tabs, we rarely get caught off guard when a customer encounters unexpected results downstream.
For every new project, time pressures loom large. One reason so many repeat customers call us is confidence that our product matches the description every time. We’ve aligned with local and international transportation rules, qualified new packaging vendors, and implemented routine process reviews—not only to fulfill regulations but to minimize pain points for the end user. When international climates throw up new challenges—trade logistics, container delays, or regulatory verification requests—we do the problem-solving ourselves instead of offloading it to intermediaries unfamiliar with either the chemistry or the end customer’s reality.
Our staff includes experienced chemical operators and technical specialists who track every stage from the first reaction flask through final packaging. Each order’s paperwork mirrors the lot’s exact process conditions, and deviations never slip past unnoticed. This attention to proper documentation, rooted in the habits of veteran chemists, safeguards both our operation and our partners down the chain.
We take every impurity profile seriously. Technical teams know that trace byproducts—halogenated side-products or over-alkylation agents—might not stand out in summary analytics but could stymie a key conversion or poison a catalyst in downstream lab work. Instead of banking on permissive industry norms for typical impurity thresholds, we set tighter internal controls and investigate every abnormal peak that shows up. Sometimes this means more hours spent in validation, but it means fewer headaches for everyone further on.
Over years of manufacturing, regulatory expectations for chemical stewardship have grown. To meet evolving global standards, we routinely audit our SOPs, effluent treatment processes, and in-plant handling practices. Colleagues in the plant receive thorough training not just for compliance, but to create a culture of mutual attention to safety. This translates directly into more consistent products—and fewer disruptions that could ripple out to customers or their own clients.
The compounds that go into Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate deserve thorough scrutiny—not just in the final product but as intermediates, solvents, and byproducts. Regular investment in air monitoring, closed transfer systems, and proper waste handling minimizes worker exposure, community risk, and regulatory surprises. Our team holds each success up to peer review, and we listen when auditors or clients spot opportunities to go further.
Each change, even minor shifts to handling or packaging material, stems from lessons learned the hard way. Whether it's a new ventilation procedure or upgrades to PPE, improvements grow from direct feedback and front-line observation. This respect for the realities of hazardous material management lives across the plant, passed down informally across shifts and reinforced by focused training initiatives—often led by workers with decades of hands-on experience.
Over the years, direct engagement with researchers has shaped both our process and our understanding of what brings value to their bench and floor. Most product improvement ideas come not from design teams, but from conversations with those who actually manipulate the product daily in their own research. Adjustments in particle size distribution, humidity controls, or specific purity requirements have all grown from frank exchanges between manufacturing engineers, bench chemists, and R&D teams at partner firms.
Some customers develop entirely new chemistries using our product as a tested stepping stone. We’re often drawn into unexpected discussions about alternative uses that hadn’t occurred to our internal team. A pharmaceutical partner may use this compound for target synthesis today, and an agricultural innovator may see a route to time-release coatings tomorrow. Each new use stretches our team to examine points of failure and opportunity in stability, packaging, and documentation.
Embracing these challenges, we aim to offer more than just a minimum viable product. By keeping records of unique batch requirements or collaborating on storage trials, we continue to support both the product’s reputation and the career efforts of those staking their research on each shipment’s reliability.
With every passing year, we refine our process. Reliability stems less from flash innovations and more from a cycle of honest review, technical discipline, and adaptation to problems as they emerge. Each improvement in control over raw material quality, reaction monitoring, and packaging builds on prior effort. We document every deviation and re-examine them during periodic reviews, making sure avoidable mistakes become rare events.
Sometimes, trends in research catch us by surprise. Surges in demand for greater purity or new solvent-inclusion studies—sparked by regulatory changes or discovery in the literature—test our agility. Our operational structure rewards early flagging of such shifts and empowers technical leads to dive into root-cause analysis rather than delay needed change.
Feedback cycles, internal and external, shape our approach to scale-up risk. Years ago, an ambitious production push yielded a batch with novel impurities tied to unforeseen side reactions; tracing the cause required pulling records and analyses across multiple teams. As frustrating as these episodes can be, the real value lies in the lessons drawn and the process improvements shared plant-wide afterward.
As advanced research fields evolve, demand for compounds like Ethyl N-Benzyl-N-(3,4-Dichlorophenyl)-Dl-Alaninate will only grow. We see increasing pressure on purity standards, packaging security, and traceability from farm-level applications through pharmaceutical intermediates. Our forward strategy involves regular investment in analytical capability, both for traditional attributes and emerging impurities of interest flagged by the global regulatory community.
Continued dialogue with research partners and regulatory agencies ensures we adapt approaches in-step with those we serve. Anticipating not just obvious technical hurdles, but the broader context of market entry and international compliance, has become central to plant culture.
From behind the scenes in specialty chemistry, the responsibility of safeguarding every shipment—from batch validation in the lab to final transportation and documentation—remains a hands-on art. By sticking close to the reality of daily production, and integrating lessons from every corner of the user base, we keep our product both relevant and reliable in a fast-moving landscape.