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HS Code |
854480 |
| Product Name | Ethyl L-Alaninate Hydrochloride |
| Cas Number | 13435-18-0 |
| Molecular Formula | C5H12ClNO2 |
| Molecular Weight | 153.61 g/mol |
| Appearance | White to off-white crystalline powder |
| Solubility | Soluble in water |
| Melting Point | 151-155 °C |
| Optical Activity | [α]20/D +13.0° (c=1, H2O) |
| Purity | Typically ≥98% |
| Storage Conditions | Store at 2-8°C, in a sealed container |
| Synonyms | Ethyl (S)-2-aminopropanoate hydrochloride |
| Smiles | CCOC(C)N.Cl |
As an accredited Ethyl L-Alaninate Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The packaging for Ethyl L-Alaninate Hydrochloride, 25g, features a sealed amber glass bottle with a secure screw cap and tamper-evident seal. |
| Shipping | Ethyl L-Alaninate Hydrochloride is shipped in tightly sealed containers to prevent moisture absorption and contamination. It is typically packaged in labeled, chemical-resistant bottles and cushioned for safe transit. Shipping complies with relevant chemical transport regulations, including proper documentation and hazard labeling, ensuring safety and integrity during delivery. |
| Storage | Ethyl L-Alaninate Hydrochloride should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. It should be kept away from moisture and direct sunlight. Recommended storage temperature is typically at 2-8°C (refrigerated). Always follow the supplier’s safety data sheet guidelines for optimal storage conditions and handling. |
Applications of Ethyl L-Alaninate Hydrochloride in Industrial ManufacturingAs a direct manufacturer of Ethyl L-Alaninate Hydrochloride, we supply this specialty amino acid derivative to high-value downstream sectors where reliable purity, functional group integrity, and controlled performance are critical. Our material supports industrial-scale formulations that demand exact compliance, production efficiency, and traceable quality assurance from the raw material stage through to the finished product. 1. Peptide Synthesis for Pharmaceutical ActivesEthyl L-Alaninate Hydrochloride is widely used in solution-phase and solid-phase peptide manufacturing to introduce enantiomerically pure alanine units. Its hydrochloride salt form ensures predictable coupling reactions and simplifies downstream deprotection or hydrolysis procedures. Pharmaceutical companies use our product to build short and medium-chain peptides for APIs, intermediates, and reference standards where batch-to-batch consistency and regulatory traceability are mandatory. Industry compliance standards
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2. Chiral Synthesis of Agrochemical IntermediatesResearch-focused agrochemical manufacturers utilize Ethyl L-Alaninate Hydrochloride as a chiral synthon to build enantiomerically controlled intermediates for crop protection molecules. Its L-configuration provides a reliable origin for constructing stereoselective pesticide, fungicide, and herbicide scaffolds, which require robust chiral purity and process adaptability over multi-ton production campaigns. Industry compliance standards
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3. Fine Chemical Synthesis for Optical MaterialsOptoelectronics and specialty materials producers incorporate Ethyl L-Alaninate Hydrochloride for constructing functionalized monomers and chiral ligands required in liquid crystal displays (LCDs), photoresists, and specialty resins. The molecular configuration enables end-users to develop products with controlled chiral environments, essential for uniform optical performance and alignment layer functionality. Industry compliance standards
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4. Food-Grade Amino Acid Derivative for Nutraceutical PremixesIndustrially, Ethyl L-Alaninate Hydrochloride supports large-scale food and nutraceutical formulations where precise nutritional profiles and purity are required. Producers blend it as a source of bioavailable L-Alanine, especially in formulations targeting sports nutrition, clinical diets, or specialized amino acid blends, where salt forms prolong ingredient stability and ease handling. Industry compliance standards
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5. Protected Amino Acid for Small-Molecule API SynthesisActive pharmaceutical ingredient (API) manufacturers leverage Ethyl L-Alaninate Hydrochloride as an intermediate where the ethyl ester and hydrochloride salt provide selectivity in multi-step syntheses. Its use helps to introduce protected L-Alanine moieties while enabling controlled deprotection or conversion in the final synthetic steps, minimizing side reactions in high-purity drug manufacturing. Industry compliance standards
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Through years of manufacturing fine chemicals, few compounds draw as much practical interest as Ethyl L-Alaninate Hydrochloride. Chemists look for more than purity—they need confidence in stable supply, reliability from batch to batch, and consistently replicable results. Our direct experience with every stage of synthesis, from raw material handling through to packaging, shapes the way we approach the needs of laboratories and production environments. We produce Ethyl L-Alaninate Hydrochloride with the type of care only possible on the manufacturing floor. Our team has spent years refining methods in response to input from research chemists who count on their intermediates to show up exactly as described, every single time.
The specific grade we produce for Ethyl L-Alaninate Hydrochloride is characterized by a purity of not less than 98%. The hydrochloride salt form ensures good stability for storage and packaging, reducing risk of degradation, clumping, or unanticipated reactivity. This product is typically manufactured as a white to off-white crystalline powder, easy to handle in both small-scale and multi-kilogram operations. Our facilities monitor for moisture and solvent residues, so researchers receive a product that behaves predictably in aqueous or organic media.
Every kilogram we ship represents the sum of careful raw material selection, controlled processing conditions, vigilant in-process testing, and rigorous final assaying. When operating in regulated environments—whether for pharmaceutical synthesis, medicinal chemistry, or scaling up custom projects—these quality checks form the backbone of a reliable working relationship between maker and user.
Countless users rely on Ethyl L-Alaninate Hydrochloride as an amino acid derivative in peptide synthetic routes and pharmaceutical R&D. The ethyl ester group brings vital functionality to multistep syntheses, building chains where solid-phase methods or solution-based approaches demand stable, reactive intermediates. With the hydrochloride salt, the compound stays manageable for both storage and weighing—never a minor concern when some syntheses hinge on single-gram accuracy.
Peptide chemists leverage this molecule during the construction of protected L-alanine residues. It fits well into the toolbox for making specific dipeptides or as a chiral starting point for assembling enantiopure compounds. Medicinal chemists have drawn on our versions for early-stage synthesis of antiviral, antibacterial, and enzyme-inhibiting molecules. By controlling residual solvents and tracking enantiomeric ratios using optical rotation and chiral HPLC, we proactively remove the sort of variance that would otherwise complicate downstream steps or force repeated purifications.
Some users working with automated synthesizers care deeply about bulk density, flow characteristics, and static charge. The crystalline form of our Ethyl L-Alaninate Hydrochloride offers a stable physical profile, so the material doesn’t clump in hoppers or bridge in vials. That small assurance, learned through hundreds of feedback cycles and production tweaks, saves headaches for technicians focused on high-throughput library creation.
In our own experience, preparing Ethyl L-Alaninate Hydrochloride on a meaningful scale presents concrete challenges. Ethanolysis reactions must be tightly controlled, since uncontrolled heat leads to hydrolysis or racemization. We’ve built in steps for gentle cooling and rapid phase separation in our reactors, protecting L-configuration and keeping yields consistent. After neutralization and salt formation, the hydrochloride must be dried without introducing excess heat or flow-restricting fines. Every issue we’ve encountered has either found a solution, or gets documented openly for client review.
No manufacturer works in total isolation. We’ve kept close ties with academic collaborators and startup clients who point out issues as they see them, helping us refine our drying times or optimize our deprotection protocols. Regular dialogue around sample failures or batch discrepancies has led to practical improvements: redesigned filter setups, improved packaging films to prevent atmospheric moisture ingress, and detailed records for lot-to-lot comparability. Maintaining a clean, direct line of communication with the chemical community leads to better material, not just better marketing.
Some buyers ask about key differences between Ethyl L-Alaninate Hydrochloride and other related molecules: methyl esters, free amino acids, or the unhydrochlorided ethyl ester. Structural differences in the alkyl ester group—ethyl over methyl or isopropyl—directly affect reactivity, solubility, and rate of hydrolysis in intermediate steps. Users with high-temperature or basic hydrolysis environments sometimes need the slower-cleaving ethyl group to prevent premature deprotection, which can ruin whole peptide assemblies. The hydrochloride form behaves with greater predictability during dissolving, storage, and transport, vastly reducing the unpredictable gains or losses seen with the free base under typical laboratory conditions.
From the manufacturing perspective, every slight change in route or protection group carries downstream implications for purity, yield, and stability. While labs often swap out starting esters to fit a synthetic plan, we’ve seen consistent calls for hydrochloride salts among researchers scaling routes for pilot or commercial supply. The salt often remains the form of record in regulatory or patent documentation, anchoring a supply chain that can be traced and tracked by batch number and analytical certificate years after original transfer.
Batch consistency isn’t a slogan; it’s a lived challenge. Our manufacturing teams maintain logs for moisture content, optical rotation, melting point, and residual solvent profile for every run. We avoid “nominal” values that drift with warehouse conditions or analyst judgment. Routine analysis with NMR, HPLC, and polarimetry produces certainty, not surprises. This focus results from experience in troubleshooting client syntheses that veered off course because an overlooked contaminant or deviation created an invisible problem that only emerged at a late stage.
Customers who have faced sticky or off-color ethyl ester batches elsewhere report time lost to rework and cleanup. We address those weak points in process documentation and operator training, building checks for early detection of off-spec runs. We’ve added vendor qualification at the level of ethanol, alanine, and reagents—every input controlled, every change logged. Those practices reflect how hard it can be to regain trust after a batch recall or purity failure. They also explain why researchers come back after finding their milestones hit or synthesis pathways cleared.
Years of direct end-user communication have shaped the technical and operational details behind each lot of Ethyl L-Alaninate Hydrochloride. Chemists walk us through their analytical problems and preparative frustrations. When a major peptide customer flagged slight differences in melting point and solubility versus their reference standards, our entire process documentation underwent review. We pinpointed an upstream filtration variable, adjusted for particle size cutoffs, and saw subsequent complaints evaporate.
Repeat orders prompt deep dives into what keeps process flows smooth for our partners. Bulk users—up to 100 kg per purchase—need materials that handle well in their automated fraction collectors and rotovap lines. Small-scale researchers want consistency in weighing and dissolution from one week to the next. As direct producers, our only success comes from responding to that difference, not blanketing users with catalog assurances. Troubleshooting together leads to better chemistry; it also keeps us accountable.
Nothing stalls research work faster than a delayed or mismatched delivery. Our production calendars track multiple lines for Ethyl L-Alaninate Hydrochloride—pilot-scale glass reactors for rapid batches, and stainless multi-ton units for industrial runs. Flexibility comes not from stockpiles, but the ability to source and react quickly based on accepted process chemistry and scalable protocols. Priority contracts can be implemented once we confirm incoming materials and tank space, with lead times shrinking thanks to vertical stock control.
Disruptions—be it raw material shortages or utility breakdown—rarely reach customers, because redundancy in our sourcing network and equipment creates buffers. We designed our plant scheduling specifically to favor those products, like Ethyl L-Alaninate Hydrochloride, which require regular retesting and client-specific tweaks. Having machinery calibrated for small and large volumes has allowed us to supply everyone from startups synthesizing single peptides to multinationals running regular multistep productions for years.
Complete analytical records—IR, NMR, HPLC, water content, optical rotation—follow each batch to the end user. We offer full data review before shipment, including test reports for individual parameters many smaller labs often don’t have the instrumentation to check themselves. Retention samples remain on file for several years, providing reference material in case disputes or questions arise. Our approach includes more than the stated minimum; we archive manufacturing logs, sample photos, and instrument output for every lot, both for client reference and internal learning.
Repeat business thrives on openness about batch slips, changes in synthetic route, or the impact of changing a purification medium. We never move a batch out the door without cross-verifying every primary analysis, and we welcome customer audits. Researchers often ask for extended records, from solvent lot numbers to temperature logbooks for drying ovens. That scrutiny helps strengthen our own processes, by forcing us to look for oversights or errors before they reach a bench or process vessel elsewhere.
Our shopfloor experience drives us to minimize off-gassing, streamlines energy usage, and develop recycling protocols for solvents and byproduct streams. Peptide chemistry contributes to next-generation treatments in medicine, so sustainability matters at every tonne shipped. By capturing waste solvents and redesigning energy-intensive isolation steps, we’ve trimmed both the cost and environmental impact of each kilogram produced. Regular audits and third-party assessments hold us accountable when it comes to emissions and waste disposal, steering us toward lower-impact choices.
The same hands-on approach informs our packaging. We adopted resealable, moisture-resistant liners for Ethyl L-Alaninate Hydrochloride based on end-user feedback on caking in humid climates. Shipment traceability now extends to RFID and barcoded tamper-proof seals, requested by those facing regulatory scrutiny or long transit times. By listening and acting on new information as it comes, real life in the chemical plant gets sharper and more focused with every batch released.
Our journey with Ethyl L-Alaninate Hydrochloride has been shaped as much by feedback from users as by the science of synthesis itself. Dialogue with peptide chemistry groups and small-molecule innovators points us toward process and product improvements. Many of our biggest process changes came at the request of customers tackling new targets, reviewing impurities at the ppm level, or requiring new packaging for robotics and automation. We take pride in serving as a resource for troubleshooting—offering insights into reaction conditions, solubility characteristics, and analytical techniques. This collaboration has helped laboratories and manufacturing sites make the most of each batch, even as industry needs shift and regulatory requirements tighten.
As regulations around chemical handling and purity get stricter, being able to speak directly with the team actually making the compound matters. Customers, small and large, have told us that knowing the details behind each drum or bottle leads to more productive research and troubleshooting. We see our efforts as going beyond supply; it's about real knowledge sharing, guided by a respect for both chemical discipline and the practical needs of the people at the bench.
Day in and day out, the process of making Ethyl L-Alaninate Hydrochloride is built around clear communication, continuous feedback, and rigorous technical standards. As a manufacturer, every improvement we make—to yield, purity, documentation, or response to user issues—circles back to serve the advancing edge of research. We continually adapt, not simply in response to the market, but because collaboration with real users shapes better chemical production. That approach provides the assurance labs need, the flexibility industry expects, and the accountability everyone deserves.