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HS Code |
475803 |
| Product Name | D-Alanine Methyl Ester Hydrochloride |
| Cas Number | 5874-61-9 |
| Molecular Formula | C4H9NO2 · HCl |
| Molecular Weight | 139.58 g/mol |
| Appearance | White to off-white crystalline powder |
| Solubility | Soluble in water |
| Melting Point | 183-185 °C (dec.) |
| Purity | Typically ≥98% |
| Chemical Class | Amino Acid Derivative |
| Storage Conditions | Store at 2-8°C, protected from moisture |
| Synonyms | D-Alanine methyl ester hydrochloride; H-D-Ala-OMe·HCl |
As an accredited D-Alanine Methyl Ester Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | D-Alanine Methyl Ester Hydrochloride, 5g, supplied in a sealed amber glass vial with tamper-evident cap and clear labeling. |
| Shipping | **D-Alanine Methyl Ester Hydrochloride** is shipped in secure, chemical-resistant containers to prevent contamination and moisture exposure. Packaging complies with safety regulations for laboratory chemicals. The product is typically dispatched under ambient conditions, accompanied by a detailed safety data sheet (SDS) and clear labeling for safe handling and storage during transit. |
| Storage | D-Alanine Methyl Ester Hydrochloride should be stored in a tightly sealed container, protected from moisture and light. Keep it at 2–8°C (refrigerated) to maintain stability. Store away from incompatible substances such as strong oxidizers and acids. Ensure the storage area is well-ventilated, dry, and clearly labeled. Avoid repeated freeze-thaw cycles to preserve product integrity. |
Applications of D-Alanine Methyl Ester Hydrochloride in Industrial ManufacturingD-Alanine Methyl Ester Hydrochloride serves as a specialty raw material across advanced chemical and pharmaceutical production chains. With rigorous functional and purity requirements, its use is concentrated in critical synthesis and intermediate steps where stereo-specific building blocks enable downstream innovation. The following real-world downstream application scenarios reflect its industrial value chain roles, based on verified manufacturer experience and international procurement data. 1. Peptide Pharmaceutical SynthesisIn the peptide pharmaceutical sector, manufacturers select this compound as a protected D-alanine source for stepwise solid-phase and solution-phase peptide assembly. Its stability under peptide coupling conditions, combined with controlled deprotection profiles, supports precise incorporation into APIs with D-amino acid motifs, which are essential for modulating metabolic stability or biological activity. Inclusion levels depend on the desired peptide sequence and the extent of racemization control needed. Commercial peptide production lines integrate this raw material during initial coupling or segment condensation stages, followed by downstream deprotection and purification tailored for injectable, oral, or topical peptide finished dosage forms. Industry compliance standards
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2. Chiral Intermediate for Cephalosporin Antibiotic ManufactureThis material functions as a critical chiral intermediate for certain third- and fourth-generation cephalosporin synthesis, notably where D-alanine-derived side chains are required for antibacterial pharmacophore assembly. Downstream chemical manufacturers rely on its clean stereochemistry and purity profile to minimize potential for unwanted side reactions and to achieve consistent API batch yields. Its addition occurs prior to cyclization or after condensation with other beta-lactam intermediates, with the specific proportion depending on the cephalosporin analog being targeted and reaction optimization studies. Industry compliance standards
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3. Chiral Auxiliary for Agrochemical SynthesisIn modern agrochemical compound development, this compound acts as a stereochemical auxiliary for the synthesis of select herbicide and fungicide actives. Its D-configuration imparts enantioselective control, particularly in the production of amino acid-derived crop protection molecules, where geometric isomer formation must remain within strict regulatory guidelines. Agrochemical technical teams incorporate it at the stage of active intermediate coupling, especially in the synthesis of hybridized bioactive molecules, optimizing use rates for reaction scale and downstream purification needs. Industry compliance standards
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4. Intermediate for Chiral Fine Chemical SynthesisProducers of custom fine chemicals and specialty intermediates utilize this material within processes requiring highly defined D-configuration amino ester building blocks. Its role in the generation of chiral amines, ligands, and specialty monomers is driven by selectivity and compatibility with downstream derivatization chemistry. Factories adjust usage ratios depending on the desired functional group introduction, especially when developing new chemical entities for electronic, polymer, or specialty material applications. Batch records meticulously document additions at enantioselective synthesis or amidation steps, with QC procedures upholding both chemical and stereochemical identity for high-purity end-use sectors. Industry compliance standards
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Out of countless building blocks in the chemistry world, D-Alanine Methyl Ester Hydrochloride stands tall for scientists working with peptide synthesis, chiral technologies, and pharmaceuticals. As a company dedicated to consistent process excellence, we put our full weight behind its quality, knowing that the tiniest details in amino acid derivatives can make or break downstream results.
Years of hands-on experience and feedback from long-term clients have shaped what we produce: a highly pure, crystalline white powder that’s easy to weigh, dissolve, and handle in the lab or on the pilot scale. The batch-to-batch consistency is not by luck. Our model runs with rigorous in-process controls, HPLC and NMR verification, and traceability that satisfies the hardest-nosed quality auditor. We standardize particle size to minimize caking and ensure rapid dissolution in both small- and large-scale synthesis.
Chemists usually ask us about two things first: purity and stability. Each batch of D-Alanine Methyl Ester Hydrochloride boasts a typical purity above 99%, by both HPLC and optical rotation. Any moisture content is kept below 0.5%. We care about melting point consistency, with product coming in at the expected range for the compound, confirming proper salt form and lack of unwanted polymorphs. We listen to customers who stress over storage solutions. That’s why we’ve invested in tightly controlled humidity packaging and stock rotation. Pristine packaging preserves both hydrochloride and methyl ester functionalities, a must for reliable amide bond formation.
Our core production runs accommodate kilogram-scale orders, supporting commercial R&D and pilot plant demands. Over the years, small custom lots for peptide research and larger runs for generic drug synthesis have passed through our reactors, all receiving the same attention to detail. A single process engineer oversees each lot, following our standard operating procedures and documenting every deviation, no matter how minor. This level of attention comes from years of seeing how a missed step in quenching or packing can lose a customer’s trust—or a whole batch’s value.
The core customer base uses our D-Alanine Methyl Ester Hydrochloride in peptide coupling reactions, especially when stereochemical integrity and reactivity matter. It fits projects aiming for high-yield, low-side product formation, and rigorous chiral separation. Beyond peptides, we see it applied in making building blocks for antibiotics, beta-lactam rings, and potent, highly selective enzyme inhibitors. Some use it to help modify drug metabolism or as an intermediate for molecular probes. We've worked with research partners targeting rare disease therapies and with pharmaceutical companies chasing patent cliffs in the generic space. In most of these projects, users report a smoother reaction and easier downstream purification when compared to other sources of the compound. The difference often lies in the control of residual solvents and levels of inorganic salts like sodium or potassium that can sneak in.
Several team members started out synthesizing D-amino acid derivatives themselves, usually for internal R&D. We know the struggles students and professionals face with failed couplings, streaky TLC plates, or powder that won’t properly redissolve. It’s become clear over the years that differences start with the raw D-Alanine and persist right through the esterification step. Impurities, especially racemic contamination, lead to messy HPLC traces and ultimately force extra work: additional recrystallizations, re-purifications, and awkward troubleshooting sessions. Our in-house batches consistently outpace lab-grade competitors, with a focus on chiral purity that shows up in better optical rotation readings and, crucially, in better biological assay results.
Another pain point for buyers is shipment-related degradation. Less robust packaging and longer lead times can mean hydrochloride content drops, leaving behind oiliness, clumping, or discoloration—signals of a compromised batch. We have built a system for rapid delivery and climate-resistant transport, logging shipment conditions to catch issues before they turn up in the customer’s flask.
People working on peptide synthesis, fragment coupling, or scale-up reactions care about one thing above all: a project’s chance of success. From chemists down to production technicians, the difference between a reliable lot of D-Alanine Methyl Ester Hydrochloride and a questionable one appears in every subsequent step. Pure, dry, and free-flowing material speeds up weighing, minimizes errors, and helps reactions proceed smoothly. Less downtime and fewer repeat syntheses mean money saved and pressure off the team. For those aiming for regulatory submissions, impurity profiles from our product line fall well under the ICH Q3A—the regulations demanding limits for specified, unspecified, and total impurities. Our certificates of analysis get audited, so we know what goes on the page matches reality in the drum.
Feedback from users worldwide often targets not just purity, but flexibility in how they can use the product. We keep refining granulation range and explore more granular solvency testing in various organic solvents. Some researchers have called for custom salt forms or different crystalline hydrates. We take these requests seriously, running side projects that compare solubilities or reactivity profiles of different grades. Recently, a pharmaceutical partner wanted a prepackaged form tailored for their automated synthesis robots. Our technical team scaled down the packaging to match—and brought labeling and barcoding in line with their electronic tracking system. Lessons learned there have helped shape next-generation packaging and identification for all customers.
Any manufacturer can boast specification sheets, but trust gets built batch by batch, conversation by conversation. We open our doors to clients for audits and frequently share real-time process data for troubleshooting. Chemists who have seen poor or inconsistent quality from previous vendors now have a direct pipeline to a single point of contact in our technical staff. We keep records for years, if a customer wants to reference a specific batch or replicate a particularly successful synthesis pathway. Some clients need help scaling from milligrams to hundreds of grams—our technical team walks through protocols, flags possible bottlenecks, and provides advice on everything from solvent choice to purification yields.
It’s common to see labs gravitate toward the cheapest amino acid esters or those available off the shelf from bulk suppliers. We have frequently tested these alternatives in direct head-to-heads. Where others show variable water content—from subpercent to several percent—ours stays reliably dry, reducing the risk of hydrolysis before the substrate hits the coupling flask. We document every step of raw material selection, from the certified D-Alanine starter through the protection and methylation processes.
Racemic contamination is always top of mind. Lower-grade batches often measure well until optically active applications bring differences into sharp relief. In our experience, a batch with even 1-2% L-enantiomer can dramatically lower yields and wreak havoc in asymmetric syntheses. Our continuous investment in chiral resolution steps, with real-world HPLC and polarimetry, keeps contamination at bay. This speaks volumes during peptide drug discovery, where reliable stereochemistry influences activity and regulatory approval.
Years spent making and handling D-Alanine Methyl Ester Hydrochloride have taught us the small things that crop up outside textbooks: the peculiar clumping that results from storage in humid climates, the tendency for methyl esters to pick up odors if not sealed away from volatiles, and the minute pH swings that can alter reactivity in subsequent reactions. We intervene before these become problems for end users. Carefully trained plant staff rotate every packaged lot in dedicated warehouse spaces, running random spot checks for caking, color change, and container integrity.
Each reaction run starts with a full readout of prior production records. Plant engineers write up deviation reports for anything odd—a longer reaction time, a color shift in the intermediate, a filter press issue—and keep these logs open for inspection. This allows us to spot trends before they hit the bottom line. For example, switching solvent supplier after a tainted lot showed up in an early analytical batch helped avoid recurring problems. We roll findings back into our SOPs, making corrections transparent and reproducible.
End users from beyond our home lab benches have provided invaluable feedback. Some call in about unusual side products popping up during scale-up; others need data on trace impurities for submission to regulatory agencies in North America, Europe, or East Asia. We respond by sharing our in-process testing records and, when justified, extend batch analysis to cover additional substances. The result is a product line shaped not just by chemistry “best practice,” but by real user feedback and project needs.
We’ve been asked before for documentation tracing all raw materials, sometimes for patent filings or regulatory audits. We maintain a live database of every production record, which can be made available under proper confidentiality. Transparency helps our customers safeguard their own intellectual property and regulatory standing.
Shipping and compliance add their own set of hurdles. As regulations shift in major markets, customers need reassurance about origin, chain of custody, and contaminant screening—without compromising delivery timelines. Our compliance team keeps up with updates from regulatory bodies and makes rapid internal changes when necessary. This includes certifications for restricted substances, REACH compliance, and import/export documentation. We continually invest in supply chain transparency, which customers often cite as crucial for their annual audits.
We keep buffer stocks in strategically located warehouses to minimize shipping delays. Our digital tracking offers real-time shipment data, allowing clients to plan syntheses with confidence. Experience tells us that a gap in material supply can stop entire projects. We treat our delivery timelines with the same intensity as our production runs.
All manufacturing brings challenges—raw material availability, rising energy costs, and changing regulatory rules. We work closely with trusted suppliers for feedstock D-Alanine, vetting every supplier annually for quality and reliability. Volatility in methylating agents has led us to dual-source, keeping price spikes and shortages at bay. To further mitigate risk, we schedule regular plant shutdowns for maintenance and upgrades, even at the cost of short-term delays, so our equipment baseline stays modern and less prone to accidents or contamination.
A recurring issue for chemists is small, unexpected residue in large-scale peptides. When this trace contamination happens, we review every step of our synthesis and packaging until we trace the root cause. In one case, modifying the crystallization step and switching inert gas sources resolved a recurring complaint. Fielding calls from customers, we’ve developed rapid-response troubleshooting and, where necessary, batch replacement programs. Our technical experts keep up with literature, learning from incidents reported by peers, and roll preventative measures back into daily operations.
Academic and start-up partners often run lean, working with funding cycles and shifting research priorities. Providing flexible lot sizes offers young researchers access to professional-grade reagents without committing to heavy minimum orders. Over time, student feedback and university collaboration have steered improvements in our bottling processes and documentation standards.
Participation in grant-funded research sometimes calls for detailed impurity profiling and unusual packaging. We’ve customized shipments to comply with transport regulations at short notice—never easy, but essential for real progress. Lab visits and technical workshops allow us to address recurring technical questions and see new directions in peptide, drug, or enzyme catalyst research, all driven by strong, on-the-ground relationships.
Peptide and specialty synthesis continue to expand, with new therapies demanding amino acid derivatives that are even purer, more reproducible, and compatible with emerging green chemistry standards. Our in-house chemists track new developments in catalyst-free and flow synthesis methods. As demand moves toward more sustainable, less hazardous reagents, we already work to reduce residual solvents and cut down on hazardous waste in our production of D-Alanine Methyl Ester Hydrochloride. Process optimization helps us reduce water and energy usage per kilogram, and waste streams receive stricter monitoring as standard.
Downstream users will continue driving demand for tighter specifications and real-world, peer-reviewed data supporting their production choices. We share anonymized reaction data from compatible clients to help scientists in the field see how our D-Alanine Methyl Ester Hydrochloride performs, not just as a white powder but as a core tool in their synthesis toolkit.
Every order, no matter the size or destination, links us directly to innovators chasing new therapies, answers for rare diseases, or breakthroughs in material science. We see firsthand how a batch of D-Alanine Methyl Ester Hydrochloride, made the right way, can fast-track months of lab work across the globe. Our commitment stays local and personal, with a watchful eye on every lot that leaves our warehouse. From formulation to finished product, we never lose sight of the trust placed in our team.
Customers tell us the risks of unreliable supply or impurities go beyond the lab—they hit project budgets, investor confidence, and regulatory deadlines. That’s why the manufacturing process has never been about just making a white powder. The work starts early and carries through past shipping, tied tightly to every downstream experiment, every application, and every hopeful result.
To us, D-Alanine Methyl Ester Hydrochloride is more than a product listing or a line in a catalog. It carries the expectation of precision and the reality of collaboration. We stay open to change—from customer-driven tweaks to in-house process optimization. Our staff and partners keep teaching us about real-world challenges and new frontiers, driving us to refine our standards every cycle. In our business, reliability isn’t an abstract idea; it’s a recipe measured out in every gram we deliver.