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L-Cysteine Methyl Ester Hydrochloride

    • Product Name L-Cysteine Methyl Ester Hydrochloride
    • Alias L-Cys-OMe HCl
    • Einecs 248-098-3
    • 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
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    Specifications

    HS Code

    498581

    Chemical Name L-Cysteine Methyl Ester Hydrochloride
    Molecular Formula C4H9NO2S·HCl
    Molecular Weight 171.65 g/mol
    Appearance White to off-white crystalline powder
    Solubility In Water Soluble
    Melting Point 126-130°C (decomposition)
    Cas Number 868-59-7
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Synonyms L-Cysteine methyl ester hydrochloride; Methyl L-cysteinate hydrochloride
    Ph Value Approximately 2.0-3.5 (10% solution)
    Odor Slight characteristic odor
    Specific Rotation +4.0° to +7.0° (c=2, H2O)
    Usage Used as an intermediate in pharmaceuticals and peptides synthesis
    Stability Stable under recommended storage conditions

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

    Packing & Storage
    Packing White plastic bottle with screw cap, labeled “L-Cysteine Methyl Ester Hydrochloride, 100g,” includes hazard symbols and storage instructions.
    Shipping L-Cysteine Methyl Ester Hydrochloride is shipped in tightly sealed, chemical-resistant containers to prevent moisture absorption and contamination. It is transported as a non-hazardous chemical under cool, dry conditions, and away from incompatible substances. Shipping typically includes clear labeling and adherence to standard regulations for safe handling and storage during transit.
    Storage L-Cysteine Methyl Ester Hydrochloride should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from direct sunlight, heat, and moisture. Store at room temperature (15–25°C) and protect from strong acids, bases, and oxidizing agents. Ensure the storage area is clearly labeled and restrict access to trained personnel.
    Application of L-Cysteine Methyl Ester Hydrochloride

    Applications of L-Cysteine Methyl Ester Hydrochloride in Industrial Manufacturing

    L-Cysteine Methyl Ester Hydrochloride serves as an essential amino acid derivative in specialized chemical synthesis and advanced industrial processes. Our clients use this material across multiple regulated sectors that require strict quality control, established compliance protocols, and precise formulation parameters. Below we detail specialized downstream applications in key industrial segments, referencing real standards, process details, and end products.

    1. Pharmaceutical Peptide Synthesis

    Major pharmaceutical manufacturers employ this compound as a high-purity protected cysteine derivative within automated peptide chain assembly and active pharmaceutical ingredient (API) development. Its methyl ester group secures efficient coupling while protecting the thiol side chain during solid-phase peptide synthesis (SPPS). Controlled release permits targeted cysteine introduction for biosimilar, insulin, and therapeutic peptide production, strictly under cGMP environments.

    Industry compliance standards

    • ICH Q7 GMP Guidelines for APIs
    • USP-NF (United States Pharmacopeia - National Formulary)
    • EU GMP Part II (ICH Q7 )
    • EP (European Pharmacopoeia) for peptide substances

    Typical usage ratio

    • Typically 0.5–10 mol% relative to the total amino acid count, adjusted based on peptide sequence and target chain length.
    • Cysteine content varies with site-specific cysteine residue requirements.

    Downstream process integration

    • Used during SPPS cycle as a protected cysteine building block.
    • Integrated through automated peptide synthesisers at coupling steps.
    • Protection removed at selective deprotection phase prior to final purification.
    • QC through HPLC and mass spectrometry post-synthesis.

    Final product types

    • Synthetic therapeutic peptides
    • Biosimilar recombinant proteins
    • Insulin analogues
    • Pharmaceutical peptide APIs

    2. Food Additive Intermediate Manufacturing

    Food ingredient manufacturers utilize this methyl ester as a precursor for synthesizing food-grade amino acid derivatives. The ester moiety imparts controlled reactivity, supporting applications like flavor precursor modification, functional ingredient fortification, and enzymatic transformation processes. Integration throughout strictly monitored food production environments ensures compliance with international food standards and traceability from source to batch release.

    Industry compliance standards

    • FCC (Food Chemicals Codex)
    • 21 CFR 172.320 (US FDA Cysteine regulations)
    • GB 2760-2014 (Chinese National Food Safety Standard for Food Additives)
    • FSSC 22000 (Food Safety System Certification)

    Typical usage ratio

    • 0.02%–0.1% w/w for flavor modification and precursor conversion systems, subject to national and customer-specific additive limits.
    • Ratios adjusted per process yield and desired flavor intensity in the end product.

    Downstream process integration

    • Employed in precursor modification for food ingredient manufacturers.
    • Entered into batch reactors for enzymatic or chemical transformation to L-cysteine or cysteine-based derivatives.
    • Quality control by HPLC and residue analysis per HACCP protocols.

    Final product types

    • Food flavoring precursors
    • Bakery flour improvers
    • Aroma enhancers for broths and bouillon
    • Amino acid nutritional supplements for fortified foods

    3. Biochemical Research Reagents

    Reagent manufacturers and biochemical research labs select this material for the synthesis of custom peptides, protein folding reagents, and in vitro diagnostic substrates. The product supports precise amino acid incorporation for controlled studies, specialized enzyme substrates, and scaffolds for biotechnology R&D, often under ISO-certified conditions. Custom purity grades enable reproducible lab-scale and pilot manufacturing.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems)
    • ISO 13485:2016 (Medical device quality for IVD components)
    • GLP (Good Laboratory Practice)
    • REACH compliance for laboratory chemicals (Europe)

    Typical usage ratio

    • 1–50 mmol/L, dependent on research protocol or peptide sequence length.
    • Adjusted for desired reactivity or specific cysteine labeling requirements.

    Downstream process integration

    • Introduced during solid and solution-phase research peptide synthesis.
    • Blended in enzyme assays or protein refolding formulations.
    • Used as a protected thiol donor or as starting material in chemical biology workflows.

    Final product types

    • Custom peptides and biomarkers
    • Protein folding and refolding buffers
    • Diagnostic substrates for assay kits
    • Enzyme labeling and detection reagents

    4. Cosmetic Active Ingredient Synthesis

    Manufacturers serving the cosmetic industry incorporate this amino acid derivative during synthesis of skin repair and anti-aging actives. Controlled addition provides a crucial source of cysteine residues for thiol-based actives, including glutathione and cysteine-rich peptide antioxidants. Regulatory frameworks require full traceability, GMP-based documentation, and demonstration of purity throughout the formulation pipeline.

    Industry compliance standards

    • ISO 22716:2007 (Cosmetic GMP)
    • EU Cosmetic Regulation (EC) No. 1223/2009
    • US FDA Voluntary Cosmetic Registration Program (VCRP)
    • China Hygiene Supervision Regulations for Cosmetics

    Typical usage ratio

    • 0.01–0.3% w/w relative to total batch mass, optimized for target active content.
    • Ratio selected based on downstream conversion yield and regulatory concentration limits in finished cosmetic.

    Downstream process integration

    • Used during the early synthesis of cosmetic actives or intermediates.
    • Added in the controlled reaction stage for generation of peptide or glutathione components.
    • Full traceability required throughout QC and batch documentation per ISO and regional cosmetic regulations.

    Final product types

    • Skin brightening and repair peptides
    • Hair restoration actives
    • Antioxidant complexes for anti-aging creams
    • High-purity amino acid additives for premium skincare formulations

    5. Specialty Chemical Synthesis

    Chemical industry clients utilize this methyl ester as a reactive intermediate while manufacturing fine chemicals, drug precursors, and heterocycle-forming agents. The protected form of cysteine allows selective incorporation without unwanted oxidation, supporting controlled downstream reactions. Stringent hazard management and safety protocols ensure secure process scale-up and repeatable batch quality.

    Industry compliance standards

    • ISO 9001:2015 for chemical manufacturing
    • REACH Registration (Europe)
    • GHS Compliance for labeling and handling
    • Responsible Care® management systems

    Typical usage ratio

    • 0.5–5 mol% relative to main synthetic pathway reagent or substrate.
    • Adjusted depending on targeted transformation and required substitution degree.

    Downstream process integration

    • Charged at stepwise alkylation, condensation, or cyclization stages.
    • Methyl ester group removed in process as dictated by final application route.
    • Monitored for purity and structural integrity during reaction progress analysis.

    Final product types

    • High-value small molecule drug intermediates
    • Cysteine-modified specialty polymers
    • Chiral ligands and auxiliaries for asymmetric synthesis
    • Sulfur-containing fine chemicals
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    Certification & Compliance
    More Introduction

    L-Cysteine Methyl Ester Hydrochloride: From Our Laboratory to Your Process

    Going Beyond the Standard—A Closer Look at L-Cysteine Methyl Ester Hydrochloride

    Our experience producing L-Cysteine Methyl Ester Hydrochloride goes well beyond shipping out white crystalline powder by the bag. Every batch walks through the same rigorous pathway—raw material screening, careful synthesis, and repeated purification—before it ever sees a drum or a barrel. The methyl ester hydrochloride form deserves this kind of scrutiny. In our line, any hint of an unwanted impurity can turn into a downstream headache or even halt a full production line for our customers.

    Over the years in production, it’s become clear that L-Cysteine Methyl Ester Hydrochloride is often misunderstood as just a simple amino acid derivative. On paper, it looks like a minor tweak to plain L-cysteine. Yet in practical terms, the methyl ester form shifts its behavior—particularly in how it interacts with organic solvents and how customers can maneuver it in multi-step synthesis. This quality has opened the door for creative approaches in both pharmaceutical and specialty application development.

    A Precise Tool for Chemical Synthesis

    In the pharmaceutical sector, this compound supports important steps where the traditional hydrochloride salt of L-cysteine simply cannot compete. Our technical teams receive regular requests from research and process engineers looking for drug intermediates that can tolerate a wider range of solvents, or that require milder acid sensitivity. The methyl ester group in our product can be selectively removed or manipulated, giving medicinal chemists a flexible approach when working with protective groups.

    Our approach in manufacturing begins with selecting L-cysteine from reliable, fully traceable sources. Inconsistent raw material can ruin downstream handling, especially in highly chiral products. By working with our established partners—sulfur suppliers and amino acid fermenters—we keep a close eye on stereochemistry and unwanted side reactions. Over the years, we’ve found that even minor impurities in the starting cysteine will track all the way through to the methyl ester, and those who’ve been burned by inconsistent quality in the past understand what a headache that brings.

    One of the main advantages lies in solubility and handling. In our facility, technicians quickly noticed that the methyl ester hydrochloride flows better and dissolves far more predictably in organic synthesis tanks than the parent amino acid. This saves time, reduces clumping, and keeps filtration steps far cleaner. Some customers used to battle sticky residues with the unesterified salt but find the methyl ester hydrochloride washes through their reactors with less loss.

    Real-World Specifications—Not Just Numbers

    Across our batches, we hold L-Cysteine Methyl Ester Hydrochloride to a tight specification on purity and moisture. We rarely get questions about why we target above 98.5% purity—those working in pharma development know full well what a low-level contaminant can mean for validation. Beyond that, we monitor specific optical rotation closely. This single measurement tells a full story: run a batch on a polarimeter, and if the result is outside of range, even by a small margin, the batch never leaves our site. Chiral purity preserves biological activity, a lesson we learned again and again from customers needing confident synthetic starting points.

    Moisture content stands out in day-to-day operations. We noticed a rise in failed dissolutions during one humid summer several years ago, traced the issue to a slip in drying conditions, and overhauled our process controls. Too much moisture changes the product's reactivity, leading to unwanted hydrolysis and the formation of byproducts. Process engineers appreciate a manufacturer who locks in this parameter—there’s no time for last-minute workarounds when a reactor is running on schedule.

    Handling qualities rank high on the practical side. L-Cysteine Methyl Ester Hydrochloride has a distinct crystalline form, not a fine dust. This matters for measured dispensing, especially at larger scales. Staff working in the plant handle tons per month, so a clumpy, easily airborne powder only invites product loss and operator risk. We fine-tune our drying to produce a free-flowing, low-static powder. This subtle detail becomes critical during process transfer and keeps batch-to-batch reproducibility strong.

    Major Uses Shaped by Real Customer Needs

    Our primary feedback comes from the pharmaceutical segment. Most requests focus on active pharmaceutical ingredient (API) intermediate manufacturing, peptide synthesis, and sometimes as a resolving agent. Customers cite reasons ranging from easier ester hydrolysis in peptide coupling steps to the need for a salt that survives pre-formulation environments. L-Cysteine Methyl Ester Hydrochloride enables certain protecting group strategies that plain L-cysteine hydrochloride cannot achieve, thanks to the controlled reactivity of the ester function.

    Beyond pharma, some clients use our product in specialty flavors and fragrance intermediates. The ester group helps modulate odor thresholds and adjust compound stability in finished products. In industry, details like this often arise in response to new regulatory requirements or new product launches that stress test how a given material behaves under heat, light, or mechanical stress.

    Another key distinction emerges in surface modification chemistry. Material scientists value the methyl ester salt when they require precise functionalization of polymers or other specialty substrates. The stability and solubility profile allows for a more targeted introduction of sulfur-containing moieties, helping to tailor final materials attributes, whether it’s for enhanced adhesion, improved biocompatibility, or new electronic properties.

    Key Differences—Why This Product Delivers More Options

    Over years of working with customers across several countries, certain patterns emerge. The methyl ester hydrochloride variant of L-cysteine does not serve as a generic substitute for traditional L-cysteine hydrochloride. Each form has a unique reactivity profile. In ester-containing compounds, customers find they can control the timing and pathway of deprotection and subsequent reactions, which is not possible with the conventional acid salt version.

    Operators in our facilities also notice the methyl ester hydrochloride’s stability in storage. While non-esterified L-cysteine salts can absorb moisture quickly and degrade, the methyl ester holds up better over months of warehousing. This stability carries through to shipping and customer stocks. Some buyers measure shelf life in weeks and others in months—consistent crystalline quality means less material loss due to caking or decomposition.

    Pharmaceutical chemists see the chemical as a convenient handle for further derivatization. Its predictable behavior under both acidic and basic conditions opens creative synthetic routes, whether they are working with peptide chains, APIs, or novel small molecules. Our own partnerships with contract research organizations have taught us that minor inconsistencies in starting material can ripple through entire drug development programs—so we lean into transparency on batch analyses and performance.

    Challenges and Lessons from the Manufacturing Floor

    No chemical plant runs without hiccups. Early trials of L-Cysteine Methyl Ester Hydrochloride would sometimes show unexpected color or clarity issues, traceable back to insufficient control over reaction time or temperature. Unlike routine commodity products, the esterification stage for this compound punishes any shortcuts. We now use automated controls for heating and agitation, as our process engineers flagged risks that could emerge if the process drifts even slightly off course.

    Seasonal shifts brought another lesson. During summer humidity spikes, drying operations need tighter control to avoid product clumping and caking. Winter brings static charge and fine dusting. Over the years, we improved our air handling systems and tweaked our drying schedules for each season. Our operators suggested improvements to anti-static packaging, and we switched over to more robust drum liners that cut waste and minimize operator contact.

    Updates from quality teams also required investment in more frequent in-process testing. Quick checks for residual solvents or acid values can catch drift early and keep the customer’s product flowing. Our technical support teams have taken the lead in giving clients access to certificate of analysis data and—if required—detailed explanations of how specific analytical parameters affect their process.

    Supporting Regulatory Compliance and User Safety

    It’s become clear over time that supporting customers involves more than just supplying chemical product. Regulatory expectations climb every year. We’ve worked closely with both local and international authorities to keep documentation up to date, whether it's for GMP guidelines or other relevant standards. The food and pharma segments in particular have zero tolerance for oversight gaps.

    Our QC team takes pride in retaining full traceability from lot number back to original raw material. This tracking builds a comfort level for customers during audits or regulatory submissions. Clients regularly request full audit trails on our batches, especially for processes destined for high-value APIs.

    Product labeling and safety data documentation have grown a lot more detailed over the years. Our safety professionals work with plant operators to confirm hazard communication and proper labeling practices. On the shop floor, updated protocols ensure operators get training on spill containment and respirator use. Employees who handle L-Cysteine Methyl Ester Hydrochloride daily have shaped the evolution of these controls, translating safety rules into practical steps.

    Continual Improvement—Built from Operator and Customer Feedback

    One advantage of being a direct manufacturer involves closing the feedback loop quickly. When a customer raises a specification or handling concern, we can take that straight to the production floor. It’s not uncommon for engineers or R&D specialists to call us with urgent questions about material compatibility, solubility in unfamiliar solvents, or new process designs. We field questions on everything from HPLC retention time to compatibility with specific reactor linings.

    This two-way exchange with customers exposes areas for process improvement. One client in the peptide synthesis market reported unpredictable ester cleavage rates, which led us to fine-tune our drying and storage conditions. In cases where particle size distribution impacts process efficiency, we consult directly with process engineers to find the right balance between free-flowing qualities and minimal dusting.

    Those who use L-Cysteine Methyl Ester Hydrochloride in scale-up scenarios count on dependable supply and reproducible properties. We’ve prioritized reliable logistics and packaging options, offering both fiber drums and high-barrier bags depending on the volume and end-use location. Problems with customs delays or shipment damage may sound like logistics-only concerns, but the reality inside a chemical plant is that interrupted supply can wreak havoc when production schedules are tightly mapped. We view reliable packaging as part of the product itself.

    Looking Ahead—Meeting Tomorrow’s Process Demands

    The market for specialty amino acid derivatives continues to evolve. Our customer portfolio pushes us into new directions every year. We field more requests for custom particle sizing, alternative salt forms, and even green synthesis approaches that reduce solvent and energy consumption. Requirements for traceability and impurity profiling are now the norm, not the exception.

    Development partners in the biopharmaceutical field ask about scalable methods using recyclable catalysts or continuous flow setups. In this fast-moving space, incremental improvements—whether in purity, solubility, or supply chain reliability—mean real advantage downstream. We keep investing in process R&D, not just for today’s standard, but for where the field is heading next. The goal isn’t just more output, but higher value proposition for customers facing new technical and regulatory challenges.

    Plant engineers and chemists keep working side by side, finding new ways to squeeze out waste, minimize rework, and support exacting customer demands. Our internal review boards meet regularly with the front-line production crew to comb through yield data, side reaction rates, and solvent recovery figures. These meetings often yield ideas not just for tighter specs, but for tools and process tweaks that make on-the-ground work safer and produce a product that’s easier for customers to use.

    Only a Real Manufacturer Knows the Difference

    Some might see L-Cysteine Methyl Ester Hydrochloride as just another chemical in a long list of catalog items. Directly producing it has revealed layer after layer of complexity that makes each batch a test of both process know-how and customer awareness. Differences from other L-cysteine derivatives are not just in the molecule itself but in the way it can change a synthetic pathway, withstand tough process conditions, or solve a recurring block in upscaling production.

    Every operator knows the pressure of a reactor feed, the frustration of sticky powders, the challenge of meeting demanding contract specs, and the importance of keeping downtime to a minimum. These experiences shape an approach to quality that cannot be matched by a trader or distributor. Each shipment of our L-Cysteine Methyl Ester Hydrochloride carries the literal mark of hands-on work, backed by a company ethos that prizes reliable partnership.

    Whether the primary use involves complex pharmaceutical intermediates, specialty flavors, or material science applications, providing a consistent, high-quality source of L-Cysteine Methyl Ester Hydrochloride brings both technical and commercial advantage. Our commitment goes beyond simply fulfilling orders—we stand ready to answer new technical challenges and support evolving customer needs, drawing on the experience gained from every batch, every customer conversation, and every improvement made along the way.