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HS Code |
275139 |
| Chemical Name | L-Aspartic Acid Diethyl Ester Hydrochloride |
| Cas Number | 14056-70-7 |
| Molecular Formula | C8H16ClNO4 |
| Molecular Weight | 225.67 g/mol |
| Appearance | White to off-white crystalline powder |
| Solubility | Soluble in water and alcohol |
| Melting Point | 118-122°C |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, in a tightly sealed container |
| Synonyms | Diethyl L-aspartate hydrochloride |
| Ph 1 Aqueous Solution | 2.0-3.0 |
| Ec Number | 237-891-2 |
As an accredited L-Aspartic Acid Diethyl Ester Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | White, crystalline powder packaged in a sealed, amber glass bottle labeled "L-Aspartic Acid Diethyl Ester Hydrochloride, 100g, for laboratory use." |
| Shipping | L-Aspartic Acid Diethyl Ester Hydrochloride is shipped in tightly sealed containers, protected from moisture and light. Packaging complies with safety regulations for chemical transport. The product is labeled with hazard information and handled as a non-hazardous substance under normal conditions, though care is taken to prevent spills or contamination during transit. |
| Storage | L-Aspartic Acid Diethyl Ester Hydrochloride should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Protect from incompatible substances such as strong oxidizers. Store at room temperature, ideally between 2–8°C (35–46°F). Ensure containers are clearly labeled and keep away from food and drink sources. |
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Purity 98%: L-Aspartic Acid Diethyl Ester Hydrochloride with purity 98% is used in peptide synthesis, where it ensures high yield and minimal by-product formation. Molecular weight 237.66 g/mol: L-Aspartic Acid Diethyl Ester Hydrochloride of molecular weight 237.66 g/mol is used in pharmaceutical intermediate preparation, where it guarantees precise dosage calculations. Melting point 132-135°C: L-Aspartic Acid Diethyl Ester Hydrochloride featuring a melting point of 132-135°C is used in chemical process optimization, where its thermal stability allows efficient solvent-free reactions. Stability temperature up to 60°C: L-Aspartic Acid Diethyl Ester Hydrochloride stable up to 60°C is used in active ingredient formulation, where it maintains chemical integrity during processing. Particle size <50 µm: L-Aspartic Acid Diethyl Ester Hydrochloride with particle size less than 50 µm is used in homogeneous solution preparation, where it promotes rapid dissolution and uniform distribution. Optical purity >99% ee: L-Aspartic Acid Diethyl Ester Hydrochloride with optical purity greater than 99% ee is used in chiral drug development, where it ensures enantiomeric specificity and enhanced therapeutic efficacy. Water content ≤0.5%: L-Aspartic Acid Diethyl Ester Hydrochloride with water content not exceeding 0.5% is used in moisture-sensitive reactions, where it minimizes risk of hydrolysis and degradation. |
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L-Aspartic Acid Diethyl Ester Hydrochloride, often simply known in labs and manufacturing spaces as a key aspartic acid derivative, doesn’t command much attention outside chemistry circles. Yet, those who’ve worked with a range of intermediates will nod at the difference the right amino acid derivative can make to both research and industrial outputs. Over years collecting flasks of white powders and clear solutions, I’ve seen this compound rise from an overlooked alternative to a staple in the search for better yields and fewer headaches in downstream processing.
Ever tried pushing a synthesis through with ordinary aspartic acid? Solubility hits like a wall. While older protocols leaned on crude, inconsistent sources, diethyl ester derivatives ease that frustration. This compound, as its name hints, carries both diethyl ester and hydrochloride functional groups, shifting how it behaves in the lab. You’ll spot it as a crystalline white solid, with a melting point often above 130°C, a clear sign you’re holding something of high purity. In the world of organic synthesis, those physical details mean cleaner separations and more predictable reactions.
This product doesn’t just find fans for its physical form. Its chemical structure makes it attractive for building more complex molecules. Pharmaceutically, researchers eye it when they need an intermediate that reduces time spent purifying every reaction stage. I remember working with peptide analogues where every day lost to another round of TLC and rotary evaporation gnawed at morale—and budgets. Switching to this ester meant fewer byproducts and smoother conversions, thanks to the blocking protection of its ester groups. Its hydrochloride form means easy handling: stable enough for benchwork yet reactive enough for synthesis.
Someone outside organic chemistry might wonder why bother going for an esterified, hydrochloride salt of an amino acid. The answer comes down to practical realities. You want straightforward weighing without humidity gumming up your powder. You’re after a substance that dissolves in reaction solvents without endless sonication and heating. This product stands out for its room temperature stability and clear dissolution in common solvents like methanol, ethanol, and sometimes even dichloromethane. In my hands, this improvement alone trimmed hours off sample preparations for HPLC and LCMS, creating more time for actual thinking—and less for managing equipment quirks.
Folks running scale-up reactions see the cost difference in solvent and energy bills drop, with higher yields of target molecules because ester groups protect sensitive sites on the parent aspartic acid during multistep syntheses. Using the diethyl ester cuts down on side reactions that often create tough-to-separate impurities. In a crowded production lab, a move like this can smooth that nerve-wracking handoff between research and pilot scale, where every extra impurity threatens timelines and project budgets.
The chemical supply space brims with variation. Companies push methyl, isopropyl, and tert-butyl esters, and for good reasons—each has its own reactivity and preferred uses. In my experience and digging through peer-reviewed studies, diethyl esters strike a balance. They resist hydrolysis during syntheses but won’t hang around forever, complicating later steps. Compared to methyl esters, where volatility creeps up during distillations, diethyl esters seem to behave themselves, offering cleaner recovery and easier removal at the end of a synthesis sequence.
Another advantage comes in crystallization. Tert-butyl esters and some other protected amino acids create glassy, sticky residues that frustrate isolation. Diethyl esters, especially in hydrochloride forms, tend to fall out of solution clearly and with manageable physical properties. Those who work in peptide chemistry see this as a small but powerful edge: less time digging at sticky residues, fewer purification passes, and ultimately, reproducible yields across repeated batches.
Some might feel these incremental improvements sound trivial until they end up chasing lost yields with less predictable reagents. On university benches and production lines, efficiency is rarely about headline-grabbing breakthroughs; it emerges from shaving minutes here or boosting consistency there. The literature backs these claims—articles in synthetic journals reference esterified aspartic acid platforms as game changers in optically pure intermediate production for food, pharma, and specialty chemicals. Unlike base amino acids that can degrade under heat or oxidize unpredictably, the hydrochloride salt provides a shelf-stable option that sidesteps degradation between shipments or even between projects.
Chemists value trust. The reputation of a raw material isn’t built on marketing but on experience: one faulty lot can burn through months of effort. Over the last decade, as regulations have tightened and documentation requirements deepened, the demand for consistently pure, well-characterized materials has only grown. Certificates of analysis with detailed chromatographic profiles are now the bare minimum, not a bonus. Users of L-Aspartic Acid Diethyl Ester Hydrochloride lean into these standards, with batch-to-batch homogeneity giving managers the confidence to commit resources without hedging on variable input quality.
Environmental performance also sits high on the list for chemical professionals today. Unlike some early-generation derivatization techniques using harsh acid chlorides or heavy metals, the production of aspartic acid esters can now run cleaner, with many suppliers adopting green chemistry routes. Reductions in hazardous byproducts make downstream disposal simpler, keeping both environmental authorities and newly minted chemists happy. In my own transition from growing up in a family of industrial workers to joining green initiatives in manufacturing, the changing approach is clear—materials that simplify waste streams and improve workplace safety draw deserved attention.
Lab safety officers and quality managers routinely check the SDS and environmental impact statements. Diethyl ester hydrochloride preps generally score better than older, less stable forms. Fewer volatile organic emissions, clear protocols for safe handling, and stable shelf lives all check boxes for organizations juggling regulatory oversight alongside business demands. Responsible sourcing improves not only the carbon footprint but also the working environment for those on the ground—something too often ignored on spreadsheets but never missed in practice.
The journey of this compound doesn’t start or stop at the standard organic chemist’s bench. Beyond pharmaceuticals, material scientists leverage its unique chemical backbone for custom polymers and specialty coatings. Sometimes, these applications don’t even get much spotlight, as they sit tucked into innovation pipelines or proprietary blends. Over time, patents and technical disclosures have cited this molecule in developing biodegradable plastics, chiral resolution aids, and agrichemical intermediates demanding robust yet cleavable protection strategies. I’ve talked to researchers at conferences who describe using diethyl esters as “the solution we never knew we needed.” That kind of organic, ground-up utility—spread by word of mouth—shows the lasting relevance of the compound.
Even in biochemistry, where enzyme modification requires careful substrate selection, protecting groups and esterified amino acids open up new doors. Being able to slip the diethyl ester form into peptide chains, control hydrolysis, and tailor cleavage reactions allows greater finesse. This flexibility can improve the design of enzyme inhibitors, receptor agonists, or probe molecules. From an academic perspective, it also lowers barriers to publishing reproducible, robust research—no more variable results from flaky, inconsistent intermediates.
The specialty chemicals market has never been simple. Global events over the past few years—supply chain gridlock, commodity price jolts, and an evolving regulatory landscape—keep procurement teams on their toes. L-Aspartic Acid Diethyl Ester Hydrochloride, like many specialty building blocks, faces these pressures. Disruptions highlight the value of having trustworthy sources and reliable production methods. Some companies have diversified their suppliers, while others have invested in local or in-house production to buffer against external shocks. From my time working between university research and partnerships with contract manufacturers, I’ve seen how critical flexibility and transparency become.
Price volatility, shifting lead times, and regional transportation bottlenecks all emphasize why the precise nature of a compound matters. It’s not enough to substitute just any derivative; each variant behaves differently under operating conditions. Those who bet on high-quality diethyl ester hydrochlorides often recoup the upfront premium with smoother operations and tighter compliance in batch production. As regulations get stricter on trace impurities and product documentation, a compound that brings clear provenance and reliable quality becomes less a luxury and more a necessity.
The value of this specific aspartic acid derivative comes into sharper focus as industries tie their future to innovation. Pharmaceutical breakthroughs depend on rapidly accessing new chemical space. The food sector leans on safe, high-purity chemical intermediates to create amino acid supplements, flavor enhancers, and nutritional products—all with rigorous safety oversight. Materials science relies on repeatable chemical platforms to produce new polymers with desirable thermal and mechanical features.
Traditional commodity chemicals can only stretch so far—specialty intermediates like this one help bridge the gap between pure academic proof-of-concept and full commercial rollout. Regulatory frameworks demand traceability and low residuals, pushing legacy reagents out when they can’t live up to new standards. New players in health and wellness, advanced coatings, and agricultural biotech benefit from intermediates whose performance has been vetted both in the literature and across multiple real-world applications.
Scientific progress rarely happens in isolation. Researchers, regulatory authorities, and supply chain experts all have a role in moving chemical manufacturing toward more sustainable and robust models. Emerging research points to the potential of bio-based production methods for aspartic acid derivatives. Fermentation, enzyme-mediated transformations, and lower-energy synthetic routes could soon cut costs and further reduce environmental impact. In collaborative projects, small changes to an intermediate or precursor echo all the way through a process, shaving off waste and improving overall resource efficiency.
There’s also attention on integration with digital tools. Material tracking, digital documentation, and blockchain verification—the new frontier for production traceability—can assure buyers of chain-of-custody in high-spec applications. Laboratory information management systems (LIMS) now often embed spectral and chromatographic data along with purchase and handling records, offering unprecedented clarity. These improvements would be hard to implement without starting from well-characterized, standardized inputs, and the best chemical intermediates are those whose properties and origins are clear from the outset.
No amount of new technology can substitute for the peace of mind that comes with working from proven, well-documented chemicals. Early in my career, I thought raw materials were commodities—swap one powdered white solid for another, and all would be well. Repeated headaches taught me better. Lost time, repeated analyses, and unpredictable results all trace back, more often than not, to that first scoop from the bottle. Peers with years in the trade quietly admit they evaluate new intermediates as much by their reputation and reliability as by their listed specifications.
This resonates especially for complex syntheses or regulated production, where one bad batch can ripple through logistics, costing time, trust, and, sometimes, hard-won contracts. L-Aspartic Acid Diethyl Ester Hydrochloride, with a strong track record for consistency and performance, has saved more than a few projects from unexpected detours. There’s no shortcut to building that kind of reputation—it comes only from years of dependable results across a wide range of applications.
Modern labs face pressure from all directions: push for greener practices, calls for transparency, and relentless demand for higher productivity. The best-performing chemical intermediates reflect these changes. They reduce waste, streamline workflow, and support regulatory compliance. In my own practice, it’s often the humble switch to a new protection group or a more robust salt form that clears the way for major progress. L-Aspartic Acid Diethyl Ester Hydrochloride illustrates how attention to these details—solubility, purity, format—can smooth the path from concept to product, lab bench to marketplace.
At a time when research budgets face scrutiny and operational resilience stands as a top concern, relying on a solid intermediate is more than a technical choice—it’s a strategic one. As the chemical industry leans into smarter, safer, and more sustainable practices, those with firsthand experience and a keen eye for dependable performance lead the charge. The results show not just in numbers, but in more predictable timelines, safer work environments, and products that meet the ever-rising expectations of customers and regulators alike.