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Cbz-Cyclohexyl-L-Glycine

    • Product Name Cbz-Cyclohexyl-L-Glycine
    • Alias z-Cycohexylgly
    • Einecs 665-014-8
    • 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

    615272

    Product Name Cbz-Cyclohexyl-L-Glycine
    Chemical Formula C16H21NO4
    Molecular Weight 291.34 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Cas Number 3938-98-9
    Melting Point 96-100°C
    Storage Temperature 2-8°C
    Solubility Soluble in DMSO, methanol, and ethanol
    Protecting Group Carbobenzoxy (Cbz)

    As an accredited Cbz-Cyclohexyl-L-Glycine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Cbz-Cyclohexyl-L-Glycine is supplied in a 5-gram amber glass bottle, securely sealed, with hazard and identification labels.
    Shipping Cbz-Cyclohexyl-L-Glycine is shipped in a secure, sealed container to prevent contamination. It is packed in accordance with chemical safety regulations, often with cold packs or in a temperature-controlled environment if necessary. Appropriate hazard labeling and documentation are included to ensure compliance with shipping standards and safe handling upon arrival.
    Storage Cbz-Cyclohexyl-L-Glycine should be stored in a tightly sealed container, protected from light and moisture. Keep at a temperature between 2–8°C (refrigerator) in a well-ventilated, dry area. Avoid exposure to excessive heat and strong oxidizing agents. Ensure proper labeling and store away from incompatible substances. Follow local regulations and safety guidelines for chemical storage.
    Application of Cbz-Cyclohexyl-L-Glycine

    Applications of Cbz-Cyclohexyl-L-Glycine in Industrial Manufacturing

    Cbz-Cyclohexyl-L-Glycine serves as a specialized non-natural amino acid intermediate with primary roles in advanced peptide synthesis, pharmaceutical APIs, biotechnological enzyme modification, and research-driven chemical manufacturing. As a direct producer, we support downstream partners seeking controlled, reproducible, and regulatory-compliant incorporation of this material into integrated industrial workflows.

    1. API Peptide Synthesis for Small Molecule Drugs

    Pharmaceutical manufacturers use Cbz-Cyclohexyl-L-Glycine as a protected unnatural amino acid fragment in the stepwise solid-phase assembly of modified peptide APIs, especially for small molecule drugs that incorporate non-canonical residues to enhance metabolic stability and target selectivity. Its cyclohexyl side group provides steric bulk, altering physicochemical properties and bioactivity profiles of therapeutic peptides. Downstream formulations often require deprotection and coupling steps managed under strict cGMP environments to ensure batch consistency and patient safety.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP General Chapter <1047> Peptide APIs
    • EDQM CEP Certification (if supplied to Europe)
    • 21 CFR Part 211 (US FDA cGMP)

    Typical usage ratio

    • 1–10 mol% of total sequence length, adjusted depending on targeted site-specific incorporation or multiple substitutions within the peptide chain.

    Downstream process integration

    • Charges as a protected monomer at initial loading, followed by iterative cycles of Fmoc deprotection and chain elongation, prior to cleavage and final purification.

    Final product types

    • Antidiabetic peptide drugs
    • Antimicrobial therapeutic peptides
    • Peptide hormone analogs with improved proteolytic resistance
    • Investigational modified peptide APIs

    2. Development of Specialty Enzyme Inhibitors

    Research and commercial laboratories utilize Cbz-Cyclohexyl-L-Glycine in the synthesis of peptidomimetic enzyme inhibitors for screening against specific proteases and other biologically relevant targets. It allows precise backbone and side chain modifications, aiding in the development of lead compounds with increased specificity and reduced off-target effects. Controlled incorporation at strategic peptide positions provides competitive inhibition parameters required by pharmaceutical R&D teams.

    Industry compliance standards

    • ISO 9001: Quality Management for R&D Laboratories
    • OECD GLP (where preclinical assays apply)
    • REACH Compliance (for EU-supplied chemicals)

    Typical usage ratio

    • 0.5–5 mol% per total peptidomimetic backbone, typically at a single or a few defined inhibitor binding motifs.

    Downstream process integration

    • Integrates during solid-phase or solution-phase peptide chain synthesis prior to final deprotection and labeling.

    Final product types

    • Protease inhibitors for drug screening platforms
    • Biological assay standard peptides
    • Structure-activity relationship compound panels
    • Reference standard peptides for diagnostic R&D

    3. Manufacturing of Diagnostic Reagents and Peptide Markers

    Producers of immunodiagnostic kits and clinical assay systems synthesize custom marker peptides using Cbz-Cyclohexyl-L-Glycine to achieve required specificity and stability for antibody-antigen interaction studies or quantitative mass spectrometric techniques. Its bulky side chain increases resistance to enzymatic degradation, critical for reagent shelf life and assay reproducibility. Controlled release of the Cbz group is timed with the final purification step to yield marker peptides of high purity required for regulated diagnostics markets.

    Industry compliance standards

    • ISO 13485: Medical Devices – Quality Management Systems
    • IVDR Regulation (EU 2017/746) for in vitro diagnostic products
    • WHO Guidelines for Biological Reagents
    • CLSI Document EP17 for Measuring Limits of Detection in Immunoassays

    Typical usage ratio

    • Varies from 1–7 mol% of peptide sequence, based on target specificity, stability requirements, and assay development parameters.

    Downstream process integration

    • Chemical coupling as a building block during stepwise assembly of synthetic peptide epitopes or markers; followed by Cbz deprotection, HPLC purification, and lyophilization for kit formulation.

    Final product types

    • Mass spectrometry calibration peptides
    • Immunoassay calibration reagents
    • Synthetic peptide tracers for ELISA kits
    • Custom peptide standards for clinical laboratories

    4. Custom Peptide Manufacturing for Research and Biotech

    Biotechnology companies and academic research facilities incorporate Cbz-Cyclohexyl-L-Glycine to design and produce research-grade peptides with defined structural modifications. These applications target protein-protein interaction studies, cell signaling investigations, and development of model molecules for preclinical work. Material quality impacts downstream bioanalytical results, requiring controlled multi-step synthesis and documentation tailored to grant-funded and publication-driven workflows.

    Industry compliance standards

    • ISO 9001:2015 Certification for custom synthesis labs
    • Material Safety Data Sheet (MSDS) compliance
    • REACH Pre-registration (for Europe-bound goods)

    Typical usage ratio

    • 1–15 mol% of target peptide, depending on complexity of the research target and required structure-activity relationships.

    Downstream process integration

    • Introduced during amino acid chain assembly; Cbz deprotection typically performed prior to downstream conjugation or biotinylation steps.

    Final product types

    • Customized research peptides
    • Peptide substrates for enzyme assays
    • Fluorescently tagged peptides for imaging
    • Modified cyclohexyl-containing sequence analogs for protein engineering
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing Cbz-Cyclohexyl-L-Glycine: A Key Building Block Crafted with Experience

    Meeting Precise Needs in Modern Peptide Synthesis

    For anyone dealing with peptide synthesis at scale, amino acid derivatives present some recurring challenges. Reliable protection, consistent purity, precise stereochemistry—these aspects shape the work whether the final application lands in pharmaceuticals, agrochemical testing, or material sciences.

    Cbz-Cyclohexyl-L-Glycine, known to many of our clients as N-Carbobenzyloxy-cyclohexylglycine or Cbz-Hcy-Gly-OH, answers specific synthetic needs. Over decades, our chemistry team honed manufacturing routes that preserve the integrity of the cyclohexyl modification, prevent side reactions during carbobenzoxy protection, and hold optical activity in every batch. This derivative brings a robust protection profile and well-characterized, reproducible reactivity during peptide coupling.

    In the industry, slight differences in an intermediate’s impurity pattern or stability can spell trouble further downstream. Our process routes start from fully validated raw materials. Each hydrolysis, protection, and crystallization step receives hands-on oversight. We monitor impurity profiles at every checkpoint—not just at final QC. That’s because downstream peptide synthesis can amplify residual traces, producing incompatibility or regulatory compliance headaches for researchers and production chemists alike. By focusing on in-process controls, we resolve problems in real time instead of letting them pile up where they’re hardest to catch.

    Cbz-Cyclohexyl-L-Glycine enters the peptide assembly stream as an N-protected, cyclic-substituted glycine. Its main role is providing steric bulk in the backbone while remaining predictable in coupling efficiency. Many customers point to its smooth behavior with standard activating agents, whether using DIC, HATU, or PyBOP—because the carbobenzoxy group shields the amine without causing unwanted acyl migration or hydrolysis under typical coupling and deprotection conditions. In side-by-side tests, this derivative holds up against analogs like Boc-protected or unprotected cyclohexylglycine, reducing time spent troubleshooting side products.

    The Nuances Behind Specifications

    Crafting Cbz-Cyclohexyl-L-Glycine to our standards involves more than simple metric checking. Specifications for purity often extend to 98 percent and above, but the story lives in the unseen details. Some labs rely on TLC and simple melting point verification, but we layer more rigorous HPLC and NMR testing to back up batch traceability. Not every peptide project needs that extra step, but researchers tackling GMP or clinical supply chains care about consistency not just within a lot but across production years.

    That’s why every run passes through controlled conditions based on our decades of work. Temperature ranges never drift outside planned load curves. Solvents and reagents come from vetted sources, and deviations, even by a fraction, send up process review flags. These tactics grew out of lessons during scale-ups for specialty pharma intermediates, where a missed impurity or poorly dissolved by-product throws off entire kilo batches. We’ve since adapted our lab learning to each campaign, continuing to raise the bar for this molecule.

    Physical handling properties also matter. The Cbz group confers improved stability and easier handling than many other protective groups. A crystalline powder at room temperature stores safely in simple containers—not every derivative offers this. For international shipments, our logistics team verifies freshness with stability studies at various climates. Each package includes a tamper seal and clear batch identification, eliminating confusion once the product arrives at customer sites.

    Real-World Benefits for Peptide Chemists

    Synthesis teams often encounter bottlenecks when switching from one protected amino acid to another. Sometimes the new piece reacts too sluggishly or demands extra purification, burning up valuable time and solvent. For Cbz-Cyclohexyl-L-Glycine, we’ve worked alongside partners in academia and industry who confirm its reactivity mirrors that of less-hindered glycine analogs, yet delivers the hydrophobic and conformational advantages sought in modern bioactive peptides.

    During SPPS (solid phase peptide synthesis), the derivative loads easily onto common resins. The coupling step doesn’t release non-specific side products, and the Cbz group stands up to extended chain assembly cycles with minimal risk of premature deprotection. This tenacity brings real value: in long sequences where error correction costs pile up, solid intermediates like Cbz-Cyclohexyl-L-Glycine keep workflows predictable and reduce repetitive troubleshooting calls. Many of our regular customers highlight not just the purity, but the time they save in repeated, multi-step projects.

    Not all amino acid suppliers control enantiopurity as closely. The L-isomer can lose optical activity if carelessness creeps into the route. Here, each batch routes through specific chiral methods, reinforced by analytical follow-ups using polarimetry and chiral HPLC. Pharmaceutical teams, especially those facing strict regulatory review, notice the difference right away: fewer headaches documenting raw material identity, fewer questions during product audit, and greater overall confidence in dossier filings.

    What Sets This Product Apart from Other Protective Groups

    In our experience, many newcomers to peptide synthesis find themselves frustrated by unpredictable performance when swapping between various N-protecting groups like Fmoc, Boc, or Cbz. Where Fmoc offers ease in base-sensitive deprotection, Cbz delivers greater stability under mildly acidic and many hydrogenation conditions. Cbz-Cyclohexyl-L-Glycine works effectively in settings where Fmoc-protected compounds fall short or risk side reactions under repetitive cycles. For customers already running protocols based around Cbz chemistry, the switch to this modified glycine proceeds seamlessly. The majority of our clients transfer conditions without major redevelopment or expensive tool-up.

    Some analogs feature bulky protecting groups that force longer coupling times or introduce solubility problems at scale. We’ve engineered the final product’s crystallinity and solubility to sit squarely within typical workflow ranges. Chemists report expected yields on regular solid supports and in liquid-phase assembly, minimizing the need to tweak solvent systems or address gelling.

    The cyclohexyl ring influences conformational preference in the finished peptide—a property actively exploited in many therapeutic and diagnostic sequences. Many research teams use the hydrophobicity of this motif to improve membrane penetration or to generate defined turn motifs within macrocycles. Unlike unprotected cyclohexylglycine, this derivative allows clean, stepwise assembly without scrambling or back-exchange during cleavage.

    Service, Support, and Responsiveness Learned on the Shop Floor

    Over years of direct manufacturing and customer engagement, one message surfaces again and again: prompt, accurate support matters almost as much as physical product quality. Orders sometimes arrive with short timelines due to shifting project phases or grant review deadlines. Our production planning team responds directly, offering next-in-line batch updates, transparent lead times, and options for express shipment. Long-term partners have us on speed dial specifically because rushed jobs receive clear, realistic answers—no wishful thinking, just transparent updates based on real production windows and historical reliability.

    Questions also arrive post-shipment. Sometimes a new research group wants reassurance on storage stability, or asks about compatibility with an unfamiliar peptide coupling route. Our technical team, built from hands-on process chemists, synthesizes the exact molecule we ship. Feedback isn’t farmed out or guessed at—it’s shared from lived experience. If a new impurity appears or a slight shift arises in NMR, our support team investigates at bench scale, and feeds findings directly back to customers in plain language.

    Beyond the Catalog: Flexibility to Support Custom Projects

    Modern peptide projects rarely follow textbook routes. Unusual side chains, non-canonical amino acids, and hybrid backbones stretch the synthetic toolbox. Recognizing this trend, our custom manufacturing branch supports tailored projects based on Cbz-Cyclohexyl-L-Glycine. Researchers request modified analogs—altered ring size, special isotope labels, or changes to crystallinity designed to mesh with proprietary purification platforms.

    Supporting these customizations requires more than equipment upgrades. Years of process optimization and troubleshooting enable us to pivot quickly, shifting plant lines or adapting existing purification systems without delays. Complex, small-lot syntheses often trip up less experienced shops, typically where unknowns in side reactions and isolation step in. We’ve seen success translating milligram discovery-phase runs into multi-kilo engineering batches, stepping through scale-up by solving unique isolation or stability challenges on the ground, rather than hoping issues evaporate at larger scale.

    Client confidentiality stands central in all custom campaigns. Each agreement comes with thorough documentation, restricted access, and just-in-time reporting to ensure every run remains secure and proprietary. Regular face-to-face meetings—or direct web conferences—help researchers follow the progress, address bottlenecks, and suggest process refinements backed by real-time data. Blending hard-won experience with transparency gives partners the confidence to grow their project ambitions.

    Understanding the Regulatory and Environmental Imperative

    Increasing regulatory scrutiny now touches every corner of industrial production, not just for the finished pharmaceuticals but for every intermediate feeding the pipeline. Decades working with regulated partners shaped our own compliance culture—every batch receives a comprehensive analytical package, and our internal traceability systems echo the highest global standards. Our teams train in current best practices for documentation, environmental protection, and waste minimization, meeting not only legal requirements but also societal expectations for stewardship.

    Cbz-Cyclohexyl-L-Glycine’s process route was designed long before mandatory audits became routine. Years ago, waste solvents, yields, and emissions were tracked to reduce both operating costs and environmental risks long-term. Now, these practices stand as baseline policy. Cycle times, energy usage, and solvent recovery rates are continuously reviewed and improved. When a customer requests a custom variant, our process engineers check environmental compatibility as closely as synthetic feasibility—there’s no sense in customizing a batch at the expense of avoidable downstream waste.

    We share environmental data transparently with partners. Whether shipping within the same continent or exporting to new regions, documentation packages disclose every substance used. Our production site underwent independent audit and ongoing certification to reinforce the trust customers place in every vial and drum they receive. By standing behind process data as well as physical specifications, we support the increasingly complex documentation flows facing global developers and regulatory teams.

    Feedback Drives Continuous Improvement

    The market for synthetic intermediates keeps shifting. Each year, new coupling agents, deprotection strategies, and automation tools force chemists to adjust classic protocols. We field feedback from across the chemical, pharmaceutical, and academic worlds, using it to refine Cbz-Cyclohexyl-L-Glycine with each production campaign. Real-world case studies—whether a scale-up challenge, a residue detection issue, or a simple storage question—help chart our R&D agenda more than any conference presentation ever could.

    Partners depend on us for stability, but they also appreciate openness to improvement. Our regular customer surveys and on-site audits produce specific suggestions, ranging from packaging tweaks to changes in drying profiles for better downstream behavior. Once, a university partner reported difficulty with static electricity during large-scale weighing. Within a quarter, our packaging line incorporated antistatic liners, fed by direct reports from our plant operators. Stories like this motivate every employee from synthesis to final shipment.

    Routine isn’t synonymous with complacency. No matter how many batches pass through our reactors, each new campaign brings an opportunity to learn and upgrade—not just for ourselves but for the specialized customers relying on our process discipline. Peer reviews, industry certifications, and supplier quality audits reinforce the attention to detail each time an order leaves our warehouse.

    In Summary: More Than Just a Building Block

    Cbz-Cyclohexyl-L-Glycine stands as more than another item in a chemical catalog. Each batch, shaped by years of hands-on manufacturing and close customer dialogue, brings dependability to complex peptide assembly. Reliable protection, high purity, and proven scalability link every kilogram produced in our facilities. The molecule’s unique structure grants new degrees of control over peptide conformation, solubility, and stability—an impact that reaches from early discovery synthesis to industrial-scale API production.

    Above all, it’s a product shaped by continuous feedback loops and technical know-how. Our chemists engage every challenge, supporting partners across the globe with both responsive service and a record of continuous improvement. In a market where new demands surface each day, those who rely on Cbz-Cyclohexyl-L-Glycine trust both the molecule and the people who manufacture it.