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H-Cys(Bzl)-OMe HCl

    • Product Name H-Cys(Bzl)-OMe HCl
    • Alias CYS-OMe
    • Einecs 211-268-4
    • 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

    781563

    Chemical Name H-Cys(Bzl)-OMe HCl
    Molecular Formula C11H15NO2S·HCl
    Molecular Weight 261.77 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in water, methanol, and ethanol
    Storage Temperature 2-8°C (refrigerated)
    Protected Group Benzyl (Bzl) on thiol group
    Amino Acid Type L-Cysteine derivative
    Acid Type Supplied as hydrochloride salt
    Functional Groups Ester (methyl), amine, thiol (protected), hydrochloride
    Cas Number 2140-53-6
    Synonyms L-Cysteine, S-benzyl-, methyl ester, hydrochloride
    Usage Peptide synthesis intermediate
    Specific Rotation +24° to +28° (c=1, MeOH)

    As an accredited H-Cys(Bzl)-OMe HCl factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The chemical is supplied in a 5g amber glass bottle with a white screw cap, labeled “H-Cys(Bzl)-OMe HCl, 5g”.
    Shipping H-Cys(Bzl)-OMe HCl is shipped in tightly sealed, chemical-resistant containers to prevent moisture and light exposure. The package is clearly labeled with hazard information and handled as a non-dangerous good under most regulations. Temperature is maintained at ambient conditions unless otherwise specified. Safety data sheets are included with each shipment.
    Storage H-Cys(Bzl)-OMe HCl should be stored in a tightly sealed container, under an inert atmosphere such as nitrogen or argon, and kept in a cool, dry place away from moisture and direct sunlight. Refrigeration (2–8°C) is recommended. The compound is sensitive to air and light; avoid prolonged exposure. Store separately from strong oxidizing agents and acids.
    Application of H-Cys(Bzl)-OMe HCl

    Applications of H-Cys(Bzl)-OMe HCl in Industrial Manufacturing

    We produce H-Cys(Bzl)-OMe HCl as a specialty amino acid derivative for controlled industrial use across peptide synthesis and medical technology. The material supports high-value downstream manufacturing where process control, purity, and compliance with international regulations remain critical.

    1. Peptide API Synthesis for Pharmaceutical Intermediates

    Pharmaceutical peptide producers rely on H-Cys(Bzl)-OMe HCl during solid-phase peptide synthesis to introduce protected cysteine residues. This allows stable assembly and prevents side reactions during chain extension and cleavage steps. We supply this material with tight batch-to-batch specifications to ensure reproducibility in regulated environments. Our customers use it in synthesis routes leading to both simple dipeptides and complex APIs, which require strict traceability and impurity profiling for eventual compliance with pharmaceutical registration processes.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 210/211
    • European Pharmacopoeia monographs for amino acids and derivatives
    • Japanese Pharmacopoeia (JP) for peptide raw materials

    Typical usage ratio

    • 0.8–1.1 molar equivalents per coupling cycle, adjusted based on peptide sequence and cysteine position

    Downstream process integration

    • Introduced during protected amino acid loading in automated peptide synthesizers via Fmoc or Boc chemistry
    • Cleavage and deprotection managed under controlled acid treatment for side-chain removal post-assembly

    Final product types

    • Pharmaceutical peptide APIs such as oxytocin, vasopressin analogs, and parathyroid hormone fragments
    • Regulatory submission intermediates for GLP and GMP process validation

    2. Custom Peptide Manufacturing for Diagnostics

    Diagnostic reagent developers consume H-Cys(Bzl)-OMe HCl to prepare peptides for in vitro diagnostic (IVD) kits, especially when cysteine is needed for site-directed labeling or conjugation. Its benzyl protection prevents premature oxidation or dimerization during synthesis and storage. Our technical support includes assisting customers with Cys-containing peptide controls within method validation and stability testing under ISO 13485 regimes, matching throughput requirements for batch diagnostics production.

    Industry compliance standards

    • ISO 13485:2016 Quality Management Systems for Medical Devices
    • CLSI GP42 (formerly NCCLS) laboratory reagent quality standards
    • REACH registration and RoHS compliance for chemical management in diagnostics

    Typical usage ratio

    • 1.0 molar equivalent per cysteine position in target peptide; excess up to 10% for sequences prone to aggregation

    Downstream process integration

    • Used in stepwise peptide chain elongation protocols, followed by conjugation steps (biotin, fluorescent probes, etc.) on post-deprotected cysteine residues

    Final product types

    • Immunoassay peptide standards
    • Fluorescently labeled antigens for ELISA and lateral-flow devices
    • Quality controls for clinical analyzers

    3. Functionalized Polymer and Hydrogel Production

    Manufacturers integrate H-Cys(Bzl)-OMe HCl during the preparation of thiol-functionalized polymers or hydrogels. Its protected cysteine group provides sites for subsequent selective deprotection and thiol-mediated crosslinking, essential for creating specialized bioactive materials. Thorough monitoring of deprotection timing and resin wash protocols ensures consistent functionalization, vital for reproducibility in biomedical device substrates or high-affinity chromatography resins.

    Industry compliance standards

    • USP Class VI Biological Reactivity Tests for polymeric materials
    • ISO 10993 Biocompatibility for medical devices
    • FDA 510(k) requirements for medical-grade polymers

    Typical usage ratio

    • 0.2–0.5% (w/w) of polymer matrix, adjusted for desired crosslink density and target mechanical strength

    Downstream process integration

    • Dissolved in monomer melt or solution for pre-polymerization mixture
    • Selective hydrogenolysis or acid treatment to expose thiol for crosslinking after polymer backbone formation

    Final product types

    • Bioactive hydrogels for cell encapsulation
    • Functional polymer beads for affinity chromatography
    • Scaffold materials in tissue engineering applications

    4. Bioconjugation Reagent Synthesis

    Producers of crosslinkers and bioconjugation reagents employ H-Cys(Bzl)-OMe HCl as a building block in multi-step synthesis of activated cysteine derivatives for site-specific protein modification. Control of the benzyl deprotection rate is necessary to time the introduction of reactive thiol functionalities, allowing selective conjugation in antibody-drug conjugates or enzyme-protein labeling. Our process development team advises on minimization of side-products and ensures pharmaceutical-grade traceability in all supplied batches.

    Industry compliance standards

    • GMP (Good Manufacturing Practice) for active intermediate and starting material production
    • ISO 9001:2015 Quality Management System for process documentation and audit trail
    • US Pharmacopeia guidelines on bioconjugate linker starting materials

    Typical usage ratio

    • Stoichiometric to the activated group; typical range 1.0–1.3 molar equivalents per reactive linker unit

    Downstream process integration

    • Inserted in early-stage synthesis of bifunctional crosslinkers, followed by controlled deprotection and coupling to proteins, peptides, or nucleic acids

    Final product types

    • Activated thiol-linker reagents for antibody-drug conjugate manufacture
    • Protein labeling intermediates
    • NHS/SMCC derivatives for targeted coupling chemistry in biologics production
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    Certification & Compliance
    More Introduction

    H-Cys(Bzl)-OMe HCl: A Closer Look from the Manufacturer’s Floor

    In our labs and production lines, H-Cys(Bzl)-OMe HCl isn’t just another code on a barrel or invoice – it’s a specialty building block that keeps finding new roles in modern peptide chemistry. Day in, day out, our teams work directly with the nuanced details that shape how H-Cys(Bzl)-OMe HCl performs in the real world, providing more than a catalog entry can ever capture. Here’s how we see it after years of hands-on manufacturing experience and working closely with research chemists and formulation teams.

    Production Insights: What Goes into H-Cys(Bzl)-OMe HCl

    We don’t treat this compound as a generic cysteine derivative. The benzyl (Bzl) protecting group and methyl ester on the molecule each play a role in how the product handles, how it reacts, how it stores, and how it behaves in solid-phase peptide synthesis (SPPS). Our plant handles protection and deprotection steps with vigorous monitoring, knowing that even subtle side impurities from over-alkylation or incomplete deprotection can mean project delays or compromised yields. Every batch that leaves our facility has been through analytical checks—HPLC, NMR, mass spectrometry—cross-referenced to results from trial peptides to ensure no unseen byproducts will show up in the customer’s final step.

    We’ve seen labs disappointed with off-spec cysteine derivatives from outside suppliers. Benzyl protection is notorious for trace level contamination if the synthesis or purification isn't optimized. In-house, our team has tuned both reaction conditions and purification steps to strip away undesired isomers and unreacted precursors. These tweaks, developed and validated by our crew, pay off in cleaner syntheses downstream, which means teams spend less time troubleshooting and re-running purification. With H-Cys(Bzl)-OMe HCl, we’ve consistently delivered over 98% purity, maintaining low moisture and keeping chloride levels strict, so the product lands in the customer’s hands oxidation-free and fully protected.

    Specifications Built to Match Real Lab Demands

    Over the years, we’ve refined the form and consistency of H-Cys(Bzl)-OMe HCl based on what chemists have actually asked for. We monitor not only purity and melting point but also make sure residual solvents don’t exceed strict limits, understanding that traces from last-step solvents like dichloromethane or ethyl acetate can create headaches in sensitive peptidic systems. The compound is shipped and stored under dry, inert atmosphere, packed to minimize light exposure and oxidation, because free thiols spoil easily and render the compound useless for SPPS.

    Packaging comes in tamper-evident, sealed bottles, with batch-specific certificates accessible anytime. We run accelerated stability studies so that researchers don’t hit unexpected changes during storage or scale-up. The molecule’s bench stability, crystalline form, and controlled particle size stem from process adjustments made during commercial production—these are details that matter when weighing out small quantities or automating charge operations.

    Direct Uses: Where H-Cys(Bzl)-OMe HCl Stands Out

    Solid-phase peptide synthesis is the main application driving demand for this product, and the benzyl-protected cysteine offers the selectivity demanded by modern stepwise assembly. In SPPS, the protection strategies are everything. The benzyl group resists most deprotection conditions but cleaves cleanly with strong acids like HF or TFA—something many alternatives can’t claim. The methyl ester, on the other hand, offers a robust handle that survives coupling and elongation steps, then removes easily when the peptide is ready for final deprotection.

    Our customers usually bring the product straight to the resin, using it for the introduction of protected cysteine at a precise sequence point. The benzyl group provides the S-protection needed for those steps that activate or modify side chains without risking unwanted oxidation. The hydrochloride salt form minimizes dust and static, making measuring and transferring easier, and enables direct weighing for solution-phase coupling—no pre-neutralization necessary compared to free base forms.

    Comparing H-Cys(Bzl)-OMe HCl to Other Products

    Not all cysteine derivatives serve the same purpose. The benzyl group offers a blend of stability and easy removal that other S-protecting groups—like Trityl or Acm—can’t always match. Many labs turn to S-Trityl or S-Acm protected cysteine for highly acid-labile peptides or segments that will see minimal harsh acid. Those groups bring their own quirks: Trityl leaves behind persistent byproducts and often suffers from mobility issues on the resin. Acm, while useful in oxidative folding and selective modification, often requires additional steps for deprotection under mild conditions and sometimes, complex oxidation chemistries.

    S-Benzyl remains popular for libraries that expect to face strong acid cleavage during the final peptide release from resin, with the added bonus of fewer “dirty” side-products. In our experience, synthon choices influence both the risk of disulfide shuffling during deprotection and the burden on downstream purification. Problems show up during scale-up—xylene residues with Bzl deprotection, or batch-to-batch inconsistency with trityl products not sufficiently pure or uniform. We developed our protocols to minimize both, integrating washing and monitoring at multiple stages.

    The methyl ester group, compared to free acid-protected cysteine synthon, is less prone to hydrolysis and easier to handle under normal humidity. Some labs prefer ethyl or t-butyl esters for specific deprotection needs, but in our repeated runs, methyl ester gives a good compromise between stability and fast deprotection during final acidolysis. We’ve found t-butyl esters tend to leave t-butyl cations that mess with certain peptide sequences, so methyl avoids those pitfalls for most standard syntheses.

    Why the Formulation Matters

    Our H-Cys(Bzl)-OMe HCl is offered strictly as a crystalline solid, not as a powder or amorphous cake. This prevents collapse or caking and extends shelf life. Clumping and loss of free-flowing properties can ruin an otherwise good project, especially when customers are using automated dosage lines in high-throughput environments. Our experience has shown that granular, uniform crystallinity translates into reliable transfers and lower losses when charging automated systems. We tune our process to remove micron-size fines and manage particle size distribution, reducing the risk of material loss on scoops, glassware, or filters.

    We purposely avoid using potential cross-reactive solvents and keep all contact equipment metal-free during key steps to prevent trace metal residues from creeping into the product. This is especially critical for cysteine derivatives, as trace metals can catalyze unwanted oxidation. Chloride salt selection follows careful titration to ensure the hydrochloride contributes only to salt stability, never to unwanted chloride-driven side reactions. These considerations aren’t theoretical; we receive, weigh, and handle every batch ourselves, making the link between bench-scale behaviors and final product performance tight.

    Problem-Solving: Batch Consistency and Reliability

    Our manufacturing team deals with real-world issues encountered by large and small research groups. Consistent batches save time and money. We track each lot back to raw materials, monitoring not just the final product but all intermediates created along the way. If a new lot of starting material displays even slight color or odor deviations, we halt the process and test in blending assays. We receive frequent feedback from repeat customers who have struggled elsewhere with darkening or uneven coloring in their protected amino acid stocks; each time, the culprit traces back to variable or impure intermediates.

    We run additional stability and forced-degradation studies on each lot of H-Cys(Bzl)-OMe HCl. Every flask and drum gets checked for water content using Karl Fischer titration, which we find essential since moisture triggers hydrolysis, oxidation, and ultimately poor coupling. On the peptide synthesis floor, these practicalities matter: a degraded or partially oxidized cysteine leads to low peptide yields or unexpected byproducts, particularly when synthesizing cysteine-rich or disulfide-containing peptides.

    Application Support: Beyond the Bottle

    We don’t just ship the compound and end the conversation. As the folks actually making H-Cys(Bzl)-OMe HCl, we know what it acts like during all typical coupling, deprotection, and purification steps. Our technical staff documents the coupling profiles, side reaction propensities, and shelf stability, sharing those findings on request. Whether customers plan a run involving large-scale peptide resin synthesis or specialized solution-phase coupling, we’ve likely seen or solved the challenge before.

    Occasionally, new application requirements prompt changes in specifications or packaging. We’ve developed special inert-atmosphere vials for high-sensitivity work and switched container linings based on observed residues, all directly in response to practical needs documented in our customers’ processes.

    Safe Handling and Storage Practices

    Cysteine derivatives like H-Cys(Bzl)-OMe HCl demand care to prevent degradation and maintain value. From start to finish, our plant avoids high humidity, excess heat, and bright light. Batches are stored and transported in nitrogen-purged, sealed packaging, often double-bagged in opaque containers to block UV exposure. Cysteine’s thiol group is among the most oxidation-sensitive functional groups we handle, and we’ve learned not to trust theoretical stability claims – we perform shelf tests under various scenarios and adapt storage and shipping practices accordingly.

    Every new customer receives best-practice recommendations based on our experience—store sealed, in a dry atmosphere, with periodic moisture checks if opened frequently. Oxidation risk increases each time the vial is accessed, making portioning into smaller containers before daily use a practical approach. These aren’t simply “recommended guidelines”; they’re techniques honed by trial and error to ensure supplied product lives up to the QC report through actual use, not just on a slip of paper.

    Supporting Advanced Peptide Research

    The landscape of peptide synthons keeps evolving, but as the producers on the ground, we notice the real differences from each production run of H-Cys(Bzl)-OMe HCl. It remains a backbone product for custom peptide synthesis, library generation, and structure-activity relationship studies. Larger-scale GMP users depend on it for regulatory studies while research labs use hundreds of milligrams per synthesis run to support novel targets or biomarker discovery.

    Our involvement doesn’t stop with batch release. As new synthetic challenges develop—such as novel cyclic peptides or proteins that demand particular oxidative folding strategies—we adapt our in-process controls and QA testing to match. When peptide purity requirements tighten, we dig deeper into impurity profiling. We connect directly with end-users during troubleshooting or new application ramp-ups, finding that the shortest route to solutions is the open line between manufacturer and bench scientist.

    Choosing the Right Supplier Counts

    With so many resellers swapping between numerous bulk manufacturers, not all H-Cys(Bzl)-OMe HCl on the market starts from the same process or achieves the critical specifications. We see differences that start with raw material sourcing—high-purity cysteine from reputable biosynthesis routes trumps variable marketplace grades. Benzyl chloride sources and methylation chemistries leave different impurity fingerprints on the product, impacting both purity and handling.

    We developed and documented all our process steps in-house, holding to proven equipment maintenance and lot tracking protocols. This isn’t a paper requirement—it keeps production repeatable and product performance reliable, as shown by multi-year feedback from universities and pharma partners who run clinical peptide projects and demand consistency. No short-cuts or substitutions. Every compound batch is traceable to source and process, meaning if challenges arise, we have answers within hours, not days.

    Regulatory and Analytical Transparency

    Regulations around protected amino acids and derivatives are moving targets, as many literature reports highlight potential regulatory scrutiny around contaminants and handling. We keep logs of all incoming materials and every process step, making sure each batch can be certified for research or GMP-related applications as standards require. Analytical transparency – detailed NMR, HPLC, MS, and moisture content reports – is handed over freely to users needing documentation for audits or method development.

    We engage third-party lab testing routinely. It’s not uncommon for even an experienced process operator to miss an impurity below 0.5%; outside verification keeps quality standards high and available at the customer’s request. If a regulatory body asks for batch traceability or in-depth impurity breakdown, we don’t scramble – that information is already tracked at each step.

    On the Horizon: Pushing for Smarter Manufacturing

    New developments in peptide synthesis keep putting more pressure on manufacturers to offer safer, cleaner, and more robust derivatives. We’re investing in stricter drying, faster packaging, and higher-purity raw material supply lines because cross-contamination and storage artifacts have caused legitimate failures in past customer projects. Upcoming syntheses using orthogonal protection schemes—where multiple protecting groups need to stay in place under varied conditions—will only succeed if the starting blocks remain clean and stable; we constantly tweak our operations to stay ahead of those trends.

    Automation and high-throughput syntheses also affect demand for physical characteristics like flowability, static control, and dust minimization. Our feedback loop from user experience on both manual and robotic systems shapes day-to-day production improvements. The signal comes directly from those making peptides for clinical or preclinical work, and from our habit of keeping the line open for detailed tech support.

    Final Thoughts: The Manufacturer’s Role in Chemistry Progress

    As the direct source for H-Cys(Bzl)-OMe HCl, we see the compound’s practical importance across research and production environments. Customers expect more than just molecular weight and a CAS number—they want reliable performance that carries over from the first milligram to kilograms needed for drug discovery or commercial scale-up. Every tweak in protection and handling learned in our own manufacturing experience translates to sharper, cleaner, and more robust results downstream.

    Meetings with research leaders, bench chemists, and formulation experts keep feeding back new requirements—sometimes pushing us to raise purity standards, other times calling for packaging innovations or assay updates. The details aren’t static; the process never really ends. We build every lot of H-Cys(Bzl)-OMe HCl for the next generation of synthetic challenges so that every project that starts with our products gets off on the right foot.