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L-Cysteine Ethyl Ester Hydrochloride

    • Product Name L-Cysteine Ethyl Ester Hydrochloride
    • Alias L-Cysteine ethyl ester HCl
    • Einecs 252-091-3
    • 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
    VTB
    Specifications

    HS Code

    201009

    Chemical Name L-Cysteine Ethyl Ester Hydrochloride
    Molecular Formula C5H11NO2S·HCl
    Molecular Weight 185.67 g/mol
    Cas Number 6224-82-6
    Appearance White to off-white crystalline powder
    Solubility Soluble in water
    Odor Slight characteristic odor
    Purity Typically ≥98%
    Storage Conditions Store in a cool, dry place, away from light
    Melting Point 93-97°C
    Ph 2.0-3.0 (1% solution in water)
    Synonyms Ethyl L-cysteinate hydrochloride
    Stability Stable under recommended storage conditions
    Grade Often available as pharmaceutical or research grade

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

    Packing & Storage
    Packing White crystalline powder packaged in a sealed 500g plastic bottle, labeled "L-Cysteine Ethyl Ester Hydrochloride," with safety and batch information.
    Shipping L-Cysteine Ethyl Ester Hydrochloride is shipped in tightly sealed containers to protect it from moisture and contamination. The chemical is packed according to standard hazardous material regulations, ensuring safe transport. Packages include clear labeling and documentation. Any temperature-sensitive requirements or special handling procedures are strictly followed during shipping.
    Storage L-Cysteine Ethyl Ester Hydrochloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect the chemical from moisture and light. Store at room temperature, ideally between 15–25°C (59–77°F). Handle and store in accordance with good laboratory practices to maintain product stability and safety.
    Application of L-Cysteine Ethyl Ester Hydrochloride

    Applications of L-Cysteine Ethyl Ester Hydrochloride in Industrial Manufacturing

    As a direct manufacturer of L-Cysteine Ethyl Ester Hydrochloride, we supply this specialty amino acid derivative to established downstream industrial sectors where its specific chemical properties support advanced formulations, compliance requirements, and high-throughput processing. The following sections outline major application scenarios, illustrating how controlled usage achieves product performance and regulatory requirements at industrial scale.

    1. Pharmaceutical Intermediate Synthesis

    Within API and finished dosage manufacturing, companies incorporate this material as an efficient chiral auxiliary and building block during peptide coupling reactions and for the preparation of specialized thiol-containing pharma intermediates. Facilities typically handle the raw material under cGMP conditions with precise measurement and real-time process monitoring to ensure consistent lot-to-lot product characteristics, crucial for regulatory approval and patient safety.

    Industry compliance standards

    • Current Good Manufacturing Practice (cGMP, 21 CFR Parts 210–211)
    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP–NF Monograph applicable for use in intermediates
    • European Pharmacopoeia (Ph. Eur.) where relevant

    Typical usage ratio

    • 0.5%–5% by reaction mass, adjusted according to the target peptide sequence and reaction conditions, with chiral purity monitored by HPLC/LC-MS at each step

    Downstream process integration

    • Added during peptide coupling or esterification steps, followed by in-process analytical verification and subsequent purification or further derivatization

    Final product types

    • Pharmaceutical intermediates for APIs—particularly those containing thiol groups
    • Peptide-based drug substances
    • Active pharmaceutical ingredients with targeted stereochemistry

    2. Food Additive for Aroma Precursors

    Food ingredient manufacturers use this compound as an effective flavor precursor in specialty seasoning and processed meat products, where its breakdown during thermal processing enhances meat-like aroma and savory notes. Strict adherence to additive limits is verified in finished goods through validated analytical methods, ensuring compliance with food safety regulations and consumer expectations.

    Industry compliance standards

    • FAO/WHO JECFA Food Additive Specifications
    • GB 2760-2024 National Food Safety Standard (China)
    • US FDA 21 CFR §172.804 (Amino acids in food)
    • FSSC 22000-certified production for traceability

    Typical usage ratio

    • 0.02%–0.12% (w/w) of total formula, varying based on meat analog type, heat processing intensity, and regulatory limits

    Downstream process integration

    • Blended into pre-cook or marination stages; reacts during Maillard process for flavor development under monitored heating profiles

    Final product types

    • Processed meat analogues (sausages, plant-based burgers)
    • Ready-to-eat soups and gravies
    • Savory seasonings and flavor concentrate bases

    3. Cosmetics and Personal Care Formulations

    Cosmetic formulators employ this ingredient as a functional component in skin and hair care products, utilizing its thiol group for targeted reactions that improve keratin restructuring or impart antioxidant properties. Quality control labs confirm trace-level impurity profiles and lot consistency to align with consumer safety and product stability requirements.

    Industry compliance standards

    • EU Cosmetic Regulation EC No. 1223/2009
    • US FDA 21 CFR Part 700 (Cosmetic regulations)
    • ISO 22716: Good Manufacturing Practices for Cosmetics
    • Health Canada Cosmetic Ingredient Hotlist

    Typical usage ratio

    • 0.01%–0.2% (w/w), determined based on product type (e.g., leave-on vs rinse-off), target performance, and regulatory thresholds for thiol compounds

    Downstream process integration

    • Added to aqueous or emulsion phase during compounding with temperature control to prevent premature oxidation, followed by homogenization and stability testing

    Final product types

    • Professional hair care formulations (e.g., restructuring creams, relaxers)
    • Dermocosmetic treatments for antioxidant support
    • Specialty face masks and serums for skin conditioning

    4. Biochemical Research and Diagnostics

    Diagnostic reagent and life science tool manufacturers utilize this specialty amino acid derivative as a precursor and stabilizer in enzyme-linked immunoassays, cell culture supplements, and nucleic acid isolation kits. The raw material’s defined purity and batch reproducibility are critical for downstream applications involving high-sensitivity detection and molecular biological reliability.

    Industry compliance standards

    • ISO 13485: Medical Devices—Quality Management Systems for IVD
    • IVDR (EU Regulation 2017/746) for in vitro diagnostics
    • USP reagent grade standards where applicable
    • OECD Guidelines for Good Laboratory Practice (GLP)

    Typical usage ratio

    • 0.005%–0.05% in buffer solutions or as needed for target enzymatic activity or redox stabilization, calibrated according to specific assay or kit design

    Downstream process integration

    • Incorporated during buffer or reagent compounding, sterilized under controlled conditions, and filled aseptically for final kit or bulk reagent packaging

    Final product types

    • Cell culture supplements for laboratory and production applications
    • Assay buffers and reagent packs for immunoassays
    • DNA/RNA isolation kits

    5. Specialty Chemical Synthesis (Electroplating Additives)

    Specialty chemical producers integrate this compound as a grain-refining and brightening agent in certain nickel and copper electroplating baths, where its thiol moiety influences metal ion reduction kinetics and deposit morphology. Quality control tracks impurity carryover, decomposition risks, and bath lifetime extension through routine bath analysis and targeted additive replenishment.

    Industry compliance standards

    • ISO 9001 (Quality Management Systems for Chemical Manufacturing)
    • REACH Registration for applicable markets
    • RoHS Directive 2011/65/EU for plated components
    • ASTM B322-15 (Cleaning and Preparation of Metals for Electroplating)

    Typical usage ratio

    • 1–10 mg/L in plating solution, adjusted based on desired surface properties, current density, and deposition rate, verified by hull cell analysis and bath monitoring

    Downstream process integration

    • Dosed directly into plating tanks or premix solutions, followed by electrical deposition cycles and routine bath maintenance checks

    Final product types

    • Nickel-plated automotive and electronic connector components
    • Decorative and functional electroplated substrates
    • Printed circuit board (PCB) metallic layers
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    Certification & Compliance
    More Introduction

    L-Cysteine Ethyl Ester Hydrochloride: A Closer Look from the Manufacturer's Bench

    What Sets Our L-Cysteine Ethyl Ester Hydrochloride Apart

    In daily production, true chemical quality and consistent performance matter most. L-Cysteine Ethyl Ester Hydrochloride, often abbreviated as LCEE HCl, comes up often in discussions with R&D labs and formulation chemists for a reason. We’ve produced this compound for years, watching its use across pharma, cosmetics, food research, and specialty chemistry grow. The draw comes down to its reliable profile and unique applications—qualities that trace back to the way we design, control, and finish each batch at our facility.

    Unlike standard cysteine or its simple derivatives, L-Cysteine Ethyl Ester Hydrochloride brings a handled reactivity and improved solubility profile because of the ethyl ester group. Chemists see it as a cleaner, less reactive alternative to cysteine itself, especially in environments where gentle but effective reactivity carries the day. Its utility doesn’t just come from being another amino acid derivative—the esterification method and meticulous purification control set it apart from routine raw materials.

    Manufacturing Experience: Achieving Consistency and Purity

    Years of batch records and audits prove again and again that purity, not just identity, drives value for end users. Esterification reactions can throw curveballs: residual acids, excess ethanol, and incomplete conversion lead to material with inconsistent qualities. Close monitoring, robust distillation, and specialized crystallization yield material that doesn’t just meet assay minimums—our lots routinely surpass common pharmaceutical and food standards. Whether the request comes from a pharma developer in Europe or a flavor house here at home, consistency and reproducibility keep partners returning.

    We’ve learned not to compromise during drying and packaging, either. LCEE HCl can clump, absorb moisture, or degrade if left exposed. Overseeing each handling step gives control over particle size and minimizes metal or residual solvent content. These points matter when your formulation blends must meet transparent label requirements, or your analytical department pushes for lower impurity thresholds.

    Technical Features: Fine-Tuned for Real-World Use

    L-Cysteine Ethyl Ester Hydrochloride’s physical specifications enable steady performance in the lab and on the plant floor. Powdered, free-flowing, typically white or nearly so, its handling fits into automated and manual processes alike. Every specification sheet means little if the material frustrates an operator or fails in pilot testing. Granulation, flow, and minimal dusting save hours on production lines and prevent expensive downtime. Nothing highlights this more than hearing from plant managers switching from low-grade lots elsewhere: less caking, quicker dissolving, fewer clean-ups.

    Controlled particle range—neither too coarse nor too fine—lets R&D teams work with predictable dissolution and blending. High solubility in water and alcohol opens up process options, whether customer needs focus on tablet pressing, liquid formulations, or intermediate reactions. With a defined melting point and a recognized molecular signature, our LCEE HCl leaves little room for surprises once validated in-house.

    Why L-Cysteine Ethyl Ester Hydrochloride Stands Out in Application

    In pharmaceutical innovation, this compound sees most use as a building block in peptidomimetic synthesis or as a chiral auxiliary. The ethyl ester protects the functional group from over-reactivity, affording synthetic pathways not easily managed with cysteine’s free acid. The resultant intermediates often display increased stability and cleaner reaction profiles. That isn’t simply speculation—years of customer data show fewer side products and cleaner final APIs. Researchers care about the difference every step makes when developing new pharmaceuticals.

    Nutraceutical and cosmetic formulators use the compound’s solubility and reactivity to enhance absorption and formulation stability. Unlike some derivatives, the ethyl ester balances lipophilicity and hydrophilicity, boosting skin penetration or bioavailability. In flavor and aroma work, LCEE HCl offers nuanced reactivity with Maillard precursors for savory or umami flavor notes. We routinely receive positive feedback about the complexity and cleanness of reaction outcomes—a testament to careful impurity management upstream.

    Learning from Real-World Feedback

    Every batch made, every client call taken, refines our approach. Customers in the pharma field often point to reproducibility and impurity profiles as chief headaches with lesser sources. They work with regulatory bodies that don’t leave much slack for deviations. Addressing this, we keep detailed batch histories, always ready to share complete impurity and trace metal analyses. The same goes for customers in the personal care space, where ingredient stewardship and traceability matter to consumers as much as regulatory authorities.

    One recurring theme in user feedback: application success lives or dies on compatibility and ease of downstream processing. Early in our development years, some formulators struggled with material from third parties that clumped, required excessive milling, or introduced unknown contaminants. These issues led us to tighten sieving, switch to more inert packaging, and institute intensive QC on every drum. Better uptime for users translates into lasting relationships—the most honest endorsement of all.

    Comparing LCEE HCl with Other Cysteine Derivatives

    By now, it’s clear that not all cysteine products suit the same roles. Plain L-cysteine hydrochloride brings a highly reactive carboxylic acid group. This can disrupt complex reaction sequences or lead to undesired byproducts. The ethyl ester group in our material serves to mask this reactivity just enough, easing the load on chemists and minimizing unwanted side reactions during synthesis.

    Contrast this with cysteine methyl ester—the methyl group brings slightly higher volatility and sometimes a less predictable hydrolysis rate. The ethyl group strikes a practical middle ground: it achieves greater stability for intermediate storage and a predictable hydrolysis profile in aqueous systems. Many flavor houses, when swapping from methyl to ethyl, report better control in sequential processing, with less loss to evaporation and waste.

    Derivative alternatives, such as N-acetyl-L-cysteine, address different endpoints altogether. NAC excels as an antioxidant and mucolytic, but it brings a distinct set of properties and stability patterns that rarely overlap with the use cases driving demand for LCEE HCl. Where the application seeks a modifiable amine group or a less aggressive acid, the ethyl ester version finds ready use.

    Handling and Storage Realities in Everyday Industry

    Beyond lab theory, material handling can make or break production. We’ve seen firsthand that improper storage—humidity, open air, and unsuitable drums—leads to caking, loss of potency, or trace decomposition. Every shipment out of our plant leaves in lined, sealed containers, monitored for moisture and temperature. This isn’t just for compliance—it directly affects how users experience the material on arrival and for months afterward.

    Technical staff at our customer sites often comment on the difference in batch-to-batch stability, especially for ongoing projects where material may sit on a shelf before use. By sticking to low moisture content and careful packaging, we help them avoid last-minute surprises during scaling. Many of our partners have shared stories where switching suppliers reduced downtime, cut waste, and eliminated a range of minor production headaches—all factors that make the difference in lean, modern operations.

    Meeting Modern Regulatory and Safety Demands

    Regulation in both pharmaceutical and food applications grows more demanding every year. Our experience shipping to international markets means each lot carries a detailed, transparent record. With regular inspections and certifications, we make it easier for clients to meet audit requirements and document safety for their own stakeholders. This means full traceability for every drum, supported with data from qualified reference labs.

    Questions about allergens, trace solvents, or heavy metals often come up, particularly for multinational customers. Decades spent harmonizing our procedures to global standards—Japanese, American, and European—ensure we’re equipped to answer tough regulatory queries with data drawn from rigorous in-house analysis. We see ourselves as part of our clients’ risk mitigation process, building reputation and trust batch by batch through direct, traceable supply.

    Supporting Innovation and Partnering with End Users

    Innovation doesn’t happen in isolation. Through years of direct collaboration, we’ve seen new uses for L-Cysteine Ethyl Ester Hydrochloride emerge that were unthinkable a decade prior. Early on, most projects centered on pharmaceutical synthesis pathways. Increasingly, our material finds its way into specialty food ingredients, cosmetic actives, and advanced materials research. Often, the push to higher purity, tighter control of particle characteristics, or more innovative packaging comes directly from partnership conversations. We field new requests for custom particle sizing and special packaging formats every quarter.

    Supporting R&D isn’t simply about shipping reference samples or providing a Certificate of Analysis. It means maintaining open lines to technical directors, supporting scale-up with tailored QC, and offering real-performance feedback from our own pilot applications. Our technical and commercial staff spend more time than ever targeting new spec challenges that directly reflect downstream user feedback—smaller particle sizes for improved dissolution in beverages, careful stabilization for longer shelf-life in personal care, and tighter impurity controls to support higher-value API synthesis.

    Sustainability and Responsible Manufacturing

    Sustainability, once a side concern, has become central in every audit and partnership review. Our own chemists work to minimize waste generated from ethyl ester processes and recover as much solvent as possible. Efficient water recycling and waste reduction strategies cut not only operational costs but also the environmental burden tied to large-scale amino acid derivative production. Many partners require full lifecycle environmental reporting—our records stand ready, reflecting low emissions and high material recovery ratios.

    Programs to replace hazardous chemicals in the esterification process continue to evolve in our plant. These improvements—driven by both regulation and internal values—ensure safer workplaces for our teams and cleaner results for our end users. Finished product safety, for both handler and consumer, isn’t up for negotiation; our protocols again and again meet or exceed occupational health benchmarks.

    Why Choosing the Right L-Cysteine Ethyl Ester Hydrochloride Source Matters

    The market continues to shift. Some operators buy solely on quoted purity, ignoring origin and process controls. Over years, we’ve seen the hidden costs that emerge down the line from those choices: raw material recalls, missed project deadlines, or untraceable contaminants. Filtering out low-grade producers, we’ve focused on transparent, accountable supply—where each batch reflects not just minimum specification, but a real, testable history.

    Leading food, pharma, and nutrition developers increasingly question provenance, ask for complete documentation, demand to know impurity profiles, and request site audits. Direct relationships with manufacturers—not brokers—deliver that confidence. They want a partner who stands by material quality, supports process troubleshooting, and adapts to new project needs with technical intimacy. This echoes daily in calls with purchasing and R&D teams—once suppliers prove they can back up promises with results, they become preferred partners for years.

    Moving Forward: Continuous Improvement and Engagement

    Our journey with L-Cysteine Ethyl Ester Hydrochloride reflects decades of learning from the entire market: bench chemists, plant operators, sourcing teams, and quality auditors. Every improvement in the material—from more precise esterification methods, to updated handling standards and packaging innovations—comes from ongoing engagement with those who actually use it. Our investment in QC and process refinement tracks directly to user needs, not just theoretical benchmarks.

    As researchers and product developers extend the boundaries of what this compound can do—deeper penetration in topical products, cleaner intermediates for pharma, new flavor notes in food—our job is to listen, adapt, and keep standards ahead of changing requirements. Chemical manufacturing at this level demands real expertise, not just in what the product is, but in what it can enable for every partner down the line. That remains the real mark of value for both producer and user.

    Summing Up the Value of L-Cysteine Ethyl Ester Hydrochloride

    Where innovation meets real-world implementation, small details matter—how the powder handles, how clean the decomposition profile appears, how few surprises arise after weeks in warehouse storage. L-Cysteine Ethyl Ester Hydrochloride doesn’t just slot in as another process chemical. Its nuanced performance, carefully controlled synthesis, and versatile utility make it a staple for teams reaching for efficiency, predictability, and value in today’s competitive, quality-driven markets. The strongest endorsement comes not through any single analysis, but through years of continuous use, repeat orders, and the trust placed in direct, long-term manufacturing relationships.