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Methyl Dl-2-Aminopropanoate Hydrochloride

    • Product Name Methyl Dl-2-Aminopropanoate Hydrochloride
    • Alias DL-Alanine methyl ester hydrochloride
    • Einecs 629-426-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry admin@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    565125

    Product Name Methyl DL-2-Aminopropanoate Hydrochloride
    Cas Number 2491-65-8
    Molecular Formula C4H10ClNO2
    Molecular Weight 139.58
    Appearance White to off-white crystalline powder
    Purity Typically ≥98%
    Melting Point 125-130°C
    Solubility Soluble in water
    Storage Conditions Store at 2-8°C, protected from light
    Synonyms DL-Alanine methyl ester hydrochloride
    Smiles COC(=O)C(N)C.Cl
    Application Organic synthesis intermediate

    As an accredited Methyl Dl-2-Aminopropanoate Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Methyl Dl-2-Aminopropanoate Hydrochloride is supplied in a sealed, amber glass bottle containing 25 grams, labeled with safety and identification details.
    Shipping Methyl Dl-2-Aminopropanoate Hydrochloride is shipped in tightly sealed containers, protected from moisture and light. It is typically packed in compliance with safety and regulatory standards, including appropriate labeling and cushioning materials. During transit, temperature control and secure packaging are maintained to ensure chemical stability and to prevent leakage or contamination.
    Storage Methyl Dl-2-Aminopropanoate Hydrochloride should be stored in a tightly sealed container, protected from moisture, humidity, and direct sunlight. Keep the container in a cool, dry, and well-ventilated area, ideally at 2–8°C (refrigerated conditions). Avoid sources of ignition and incompatible substances such as strong oxidizing agents. Ensure the chemical is clearly labeled and stored away from food and drink.
    Application of Methyl Dl-2-Aminopropanoate Hydrochloride

    Applications of Methyl Dl-2-Aminopropanoate Hydrochloride in Industrial Manufacturing

    Methyl Dl-2-Aminopropanoate Hydrochloride is an established intermediate in the synthesis and formulation of high-value specialty chemicals. As the original manufacturer, we supply this material directly to downstream industries that require verified quality and strict regulatory compliance across various industrial manufacturing sectors.

    1. Pharmaceutical Active Ingredient Synthesis

    Major API producers use Methyl Dl-2-Aminopropanoate Hydrochloride as a structural intermediate in the preparation of chiral and achiral α-amino acid derivatives. It plays a critical role in esterification and amidation routes for synthesizing pharmaceutical agents, particularly those targeting neurological and metabolic pathways. In GMP environments, the material enters the process at early-stage synthesis, requiring traceable lot control and impurity profiling to comply with finished drug requirements. The downstream chemistry often includes catalytic hydrogenation, hydrolysis, or coupling with acid chlorides. Operators adjust charge ratios per route selectivity and pharma-grade specifications. Finished APIs undergo multi-stage purification before release for drug formulation.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US Pharmacopeia (USP) standards for synthesis intermediates
    • European Pharmacopoeia (Ph. Eur.) quality specifications
    • FDA 21 CFR Part 210/211 cGMP for finished pharmaceuticals

    Typical usage ratio

    • 0.9–1.2 molar equivalents against target acid or amine, typically adjusted according to specific reaction stoichiometry and targeted impurity limits within 0.5% variance

    Downstream process integration

    • Direct charge into esterification or amidation reaction vessels during stepwise API synthesis, preceded by raw material identity and purity verification in compliance with GMP requirements

    Final product types

    • Active pharmaceutical ingredient intermediates and bulk APIs (e.g., amino acid-based compounds, neuroactive drugs, peptidomimetic molecules)

    2. Peptide and Oligopeptide Production

    Peptide manufacturing companies incorporate Methyl Dl-2-Aminopropanoate Hydrochloride as a protected amino acid methyl ester input for solid-phase and solution-phase peptide synthesis. The raw material provides the required functionality for building non-proteinogenic peptide segments in research-grade and clinical-scale manufacturing environments. Technicians integrate the compound in the amino acid activation and coupling stages, with attention to the minimization of racemization and hydrolysis. The process dictates precise management of molar application, washing, and cleavage cycles to maintain peptide sequence fidelity. All batches undergo in-process testing for reaction completion and residual contaminant levels under peptide GMP guidelines.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • GMP regulations for peptide APIs (FDA, EMA)
    • ISO 9001:2015 for quality management in custom peptide synthesis

    Typical usage ratio

    • 1.0–1.1 equivalents per targeted amino acid residue, optimized based on coupling efficiency and specific peptide length, with adjustments for side-product suppression

    Downstream process integration

    • Used at initial loading or during stepwise chain elongation in solid-phase peptide synthesizers or solution-phase coupling reactors, followed by standard deprotection and purification protocols

    Final product types

    • Therapeutic peptides, peptide conjugates for diagnostics, research-grade peptide libraries, and pharmaceutical-grade oligopeptides

    3. Agrochemical Intermediate Manufacturing

    Manufacturers of high-value agrochemical products employ this material to build β-amino acid-derived herbicide and pesticide intermediates via selective aminomethylation and transesterification reactions. The raw material’s reactivity supports targeted modifications during intermediate synthesis, allowing for the fine-tuning of structure-activity profiles required in modern crop protection active ingredients. Formulators precisely meter dosage according to downstream pathway yields, maintaining tight control over process impurities and unreacted starting materials. All process steps—charging, catalyst addition, downstream separation—adhere to environmentally regulated and occupational safety frameworks for agricultural chemical manufacturing.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (Regulation (EC) No 1907/2006) for agrochemical substances in Europe
    • ISO 9001:2015 certified production for agrochemical intermediates
    • US EPA Pesticide Registration requirements

    Typical usage ratio

    • 5–15% by weight relative to other active reactants, or 1.05–1.15 molar equivalents based on targeted intermediate; dosage adjustment based on conversion rates and downstream impurity tolerance

    Downstream process integration

    • Introduced during intermediate step synthesis prior to ester hydrolysis and final formulation; material handling and mixing performed under controlled temperature and ventilation per agrochemical plant SOPs

    Final product types

    • Key intermediates for selective herbicides, fungicide scaffolds, β-amino acid-based pesticide actives

    4. Fine Chemical and Specialty Ester Synthesis

    Producers of specialty esters and fine chemicals use Methyl Dl-2-Aminopropanoate Hydrochloride in the tailored production of functionalized molecules serving advanced materials, coatings, or analytical reference chemicals. The raw material enters condensation and substitution reactions for making β-alanine esters, which serve as chain extenders or reactive monomers. Operators control the ratio according to process throughput and final product specification, routinely testing for yield, purity, and side-reaction byproducts. Production integrates continuous flow or batch operations depending on end-use markets, stressing documentation for batch traceability and compliance with chemical safety regulations.

    Industry compliance standards

    • ISO 9001:2015 for fine chemicals manufacturing
    • OECD Good Laboratory Practice (GLP) for reference chemicals
    • REACH (EC No 1907/2006) registration for specialty esters

    Typical usage ratio

    • 3–10% by mass of total reaction input in ester synthesis, with process-specific optimization to minimize excess starting material and improve downstream purification

    Downstream process integration

    • Added to reaction vessels following initial substrate charging, typically before temperature ramp and catalyst introduction; entry point dictated by batch or continuous operating conditions

    Final product types

    • Functional β-alanine esters, specialty resin precursors, analytical reagents, and industrial additive components
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    Certification & Compliance
    More Introduction

    Methyl Dl-2-Aminopropanoate Hydrochloride: Practical Insights from a Manufacturer's Perspective

    Hands-on Experience with Methyl Dl-2-Aminopropanoate Hydrochloride

    In our lab and on the factory floor, we work with a range of amino acid derivatives every day. Methyl Dl-2-Aminopropanoate Hydrochloride (CAS: 35937-09-2) stands out as an intermediate that continues to prove its usefulness in synthesis work. This particular compound, often classified as a methylated alanine ester in hydrochloride salt form, fits into a unique niche where stability and reactivity both matter. Over decades in chemical production, products like this have directly driven cost-effectiveness and consistency in pharmaceutical processes, agrochemical development, and research applications.

    We produce Methyl Dl-2-Aminopropanoate Hydrochloride in technical and high-purity grades, offering a white to off-white crystalline powder, with purity levels above 98% by HPLC. Our batches stick to this specification because our customers rely on reproducibility. A deviation of even half a percent in purity has downstream effects; anyone who’s run a catalytic step or sensitive coupling knows the frustration of chasing a source of variability that began at the raw material stage.

    Why Specification Choices Matter in Real-World Settings

    The form of this product as a hydrochloride salt really matters in practical use. The salt offers greater solubility and a lower risk of decomposition compared to the free base or ester itself. High moisture areas or inconsistent shipping environments can degrade some similar products. The hydrochloride form is robust, survives transit, and resists yellowing that sometimes appears if storage goes wrong. Many customers in global markets have told us that batches from other sources showed clumping or changes in appearance. In years of manufacturing, we have controlled for particle size, minimizing this kind of variability down the line.

    Each gram of Methyl Dl-2-Aminopropanoate Hydrochloride ties into reaction-specific needs. In peptide synthesis, it serves as a building block, and reliable ester hydrolysis is vital. In pharma intermediates, purity takes precedence—the difference between 98% and 95% often determines whether a QC team will have a smooth week or a headache with byproduct peaks in their chromatograms. Researchers making advanced structures find that lower impurity profiles allow for faster purification later. Side-product formation often correlates directly with the initial raw material grade.

    Distinguishing Features: Not All Amino Ester Salts Are Equal

    Some alternatives float around in the market—other methyl esters, ethyl esters, even sodium or potassium salt forms. Comparing these, stability jumps out straight away. Methyl esters tend to be less prone to side hydrolysis than ethyl; they keep a sharper melting point, which helps in lot-to-lot consistency. Free bases arrive with wide pH drifts (and sometimes off-odors), especially after extended storage. The hydrochloride salt lets us package tighter every time.

    From direct customer feedback, we see a lower incidence of failed batches with the hydrochloride product versus comparable amine free bases. Chemists in the pharmaceutical sector, especially those scaling up, report that the HCl salt lets them eliminate an extra neutralization step and delivers reproducible crystal qualities for solid-phase synthesis.

    Supply chain reliability has grown into a big topic, particularly in the past few years. Some competitors cut corners on the final drying phase or skip key purification cycles. What looks like a minor tweak—a shortcut past azeotropic drying, for instance—has led to massive reprocessing down the stream for their customers. We stick with a longer protocol because it works out cheaper in the real world; the cost of discarding a failed kilo batch towers over the savings in power or solvent.

    Everyday Challenges and Real Solutions in Manufacturing

    Anyone who has operated a reactor with amino acid derivatives knows they are sensitive to slight moisture exposure. Controlling relative humidity in large-scale facilities requires more than just basic climate control. We invested in dedicated dehumidification to keep our stock rooms under 35% RH, which keeps our hydrochloride salt in free-flowing, non-caking form. Regular checks and spot QC samples catch potential issues before shipping, not after.

    Batch records show that cross-contamination with other amino esters sometimes plagues bulk suppliers who chase volume over accuracy. Our facility maintains separated lines for methyl ester products. We regularly swab and validate with in-process controls—not because someone at an audit desk demanded it, but because end users notice if their material isn’t clean.

    Market pressures favor shortcuts. We have seen copycat production attempts using substandard methylating agents, introducing off-flavors or colored impurities to the product. Sticking with pure, well-characterized reagents for methylation keeps our hydrochloride product clear and odorless, which research clients appreciate. There is nothing more deflating than unsealing a new drum and finding unexpected off-white material, especially when tight project timelines are on the line.

    Meeting the Growing Demands of Synthesis Research

    Research applications have always driven evolution in our production process. Peptide chemistry, asymmetric synthesis, and intricate alkaloid work all use our Methyl Dl-2-Aminopropanoate Hydrochloride. Most recent trends in peptide APIs put pressure on raw material consistency. We get requests from both pilot plants and academic groups who ask for smaller lot sizes, sometimes as little as 100g, all traceable to the same QC records as a 25kg drum. Flexibility in packaging and certification isn’t just a talking point—it traces back to decisive shifts in customer needs.

    Quality complaints tend to cluster around substandard imports or poorly stored local stocks. We carry out shelf-life studies in real time, not just rely on vendor-provided stability data. Pulling old retained samples and running HPLC, Karl Fischer, and visual inspections every quarter has taught us a lot about long-term stability. We often find that the shelf-life stretches well past stated values if materials are handled properly. This reduces waste and helps our customers budget for bulk ordering.

    Regulatory and Traceability Considerations

    Many customers work under tight regulatory frameworks—cGMP, ISO, and REACH. Documentation standards across regions often require different paperwork, but the real test is traceability. From our perspective as a manufacturer, traceability goes beyond a printed CoA. Any deviation in raw input, batch process, or warehouse temperature needs recording. When something enters the audit trail, missing paperwork can cripple production downstream. We keep batch records, in-process QC documents, and shipping records for years, accessible any time an end-user faces a question from their own auditors.

    Over years, we have fielded queries about DMF numbers, compliance certifications, and heavy metal content. Rather than scrambling to backfill paperwork later, we build these into our routine processes. One pharmacopoeia monograph rarely fits every global customer, so we routinely adapt documentation for different end-markets.

    Handling hazardous goods brings another layer of regulation. Because Methyl Dl-2-Aminopropanoate Hydrochloride falls under category 6.1 for transport in many cases, our logistics staff undergo regular training and refresher courses covering labeling, segregation, and emergency procedures. This serves not just regulatory compliance—our customer partners feel more confident knowing that the supply arrives without incident, time after time.

    Differences from Competing Products: Beyond a Tech Spec Sheet

    Many raw material purchasers look at a few headline figures: assay percent, water content, and melting point. Experience on the ground says there’s more to the story. Products synthesized using impure starting methyl amino esters frequently show carry-over of by-products, some of which can pose real trouble for scale-up or sensitive downstream processes. We control every step of manufacture to suppress side-products. For example, chiral purity may not be mission critical for non-pharma uses but is a must-have for some advanced research.

    We often get asked why we standardize on the hydrochloride salt. The answer comes from seeing issues in actual use. Free amines take up CO2 and moisture, forming greasy carbamates that affect measured purity. Our hydrochloride salt keeps free of these trace byproducts. We get fewer returns and fewer complaints about changes in melting behavior. Some imports show a persistent, sulfurous odor—a telltale marker of using unrefined or contaminated starting materials. Our process follows a clear, verified path from raw inputs to finished goods.

    Supporting Emerging Technologies

    Recent developments in automated peptide synthesis and combinatorial chemistry place fresh demands on raw material suppliers. For semiautomated systems to run without interruption, the starting acid, base, and ester derivatives must dissolve predictably and react as anticipated. We supply material with a consistent particle profile, tested at every production campaign. People building libraries of analogues with sensitive functionality avoid our competitors’ non-standard lots after running into delays or reaction failures due to inconsistent quality.

    Greater focus in life sciences on chirality led us to invest in analytical capabilities years ago. Enantioselective LC and chiral HPLC let us support research labs that ask for precise D-/L- ratio documentation. By offering both DL and optically enriched products, we meet needs that range from general intermediate synthesis to advanced stereochemistry projects.

    Practical Limitations and Real-World Advice

    No single product suits every application. Methyl Dl-2-Aminopropanoate Hydrochloride excels in certain syntheses, but for others, customers might find aqueous solutions or free base forms more suitable. For labs operating at high-throughput or using ultra-short synthesis cycles, ready-to-use liquid forms may reduce manual labor. On the flip side, dry hydrochloride powder packs the most stability per shipment, making it a steady choice for remote operations or facilities where storage environments vary.

    Minimizing risk comes down to robust partnerships between supplier and user. We train technical support teams who actually worked in our own plant, not just sales personnel. When end-users encounter issues, they speak to people who have seen the problems firsthand and can suggest practical solutions, such as adjusting pH in early extraction steps or tweaking workup protocols to handle the salt effect.

    Feedback Loops: Learning from Customer Experience

    Nothing beats experienced eyes in the field. We benefit most from detailed feedback—chromatograms that show minor impurities, emails about handling challenges, even snapshots of packed drums after shipping. Routine calls with repeat clients often turn up subtle trends. For example, several large-scale sites observed slight changes in filterability depending on humidity at unloading. We responded by modifying drum liners and suggested alternate filtration setup. This level of interaction closes the loop between what we make and how it is used.

    Academic users in particular have flagged requests for alternate pack sizes, documentation for grant reporting, and detailed impurity breakdowns. We shifted to include small-lot production, same-day dispatch, and lot-specific documentation for these users. Our early reluctance gave way once we saw the real benefit for researchers working with narrow budgets and aggressive project deadlines.

    Environmental and Safety Considerations

    All manufacturing generates waste—sometimes as spent solvents, sometimes as process water. We engineer steps to recover and re-use solvents where feasible, cutting down both costs and emissions. By monitoring waste output and adjusting protocols based on seasonal changes in plant conditions, we further increase efficiency. Safety comes from attention to housekeeping, both in the plant and storage areas. Drum handling, powder transfer, and packaging routines come from hands-on experience, not just compliance documents.

    We encourage customers to store this product in sealed containers, away from water and uncontrolled temperature changes. Clear, tight seals keep atmospheric moisture out, preventing clumping and discoloration even in non-ideal storage. Simple practices—label checks before decanting, dedicated scoops, detailed cleaning logs—maintain batch purity and protect against cross-contamination.

    Trust Built on Process and Transparency

    Trust doesn’t come from marketing slogans. It grows from every lot that arrives on spec, every question answered by staff who know the process firsthand. We stand behind our shipments with documentation, on-the-spot analysis, and a willingness to address concerns long after the invoice closes. Feedback consistently tells us that consistent quality catches most clients’ attention, but transparency and willingness to solve issues turn a one-time buyer into a repeat customer.

    In practice, every production run adds to our understanding of where things go right and where subtle improvements are possible. For decades, our focus has stayed on steady improvements rather than chasing fads or exaggerating features. When someone asks about the practical differences in Methyl Dl-2-Aminopropanoate Hydrochloride compared to competitive offerings, we point directly to the long-term results seen in our customers’ operations—not empty promises on a sales sheet.

    Conclusion: Experience Drives Product Evolution

    Looking back, it’s clear that the most useful features—batch consistency, reliable shipment, robust stability—come from experience producing this compound at scale. Listening to real-world users, learning from laboratory-scale mishaps, and applying these lessons in bulk production keep our Methyl Dl-2-Aminopropanoate Hydrochloride at the standard we originally set: a trusted intermediate for synthesis, made by a team with hands-on expertise and a long view on what matters in daily chemical work.