Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing admin@sinochem-nanjing.com 3389378665@qq.com
Follow us:

Cbz-L-Glu-OH

    • Product Name Cbz-L-Glu-OH
    • Alias Z-E-OH
    • Einecs 211-487-0
    • 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

    768109

    product_name Cbz-L-Glu-OH
    synonyms Carbobenzyloxy-L-glutamic acid
    CAS_number 1428-72-8
    molecular_formula C12H13NO6
    molecular_weight 267.24
    appearance White to off-white powder
    purity Typically ≥98%
    storage_temperature 2-8°C
    solubility Slightly soluble in water, soluble in organic solvents like methanol or ethanol
    SMILES C1=CC=C(C=C1)COC(=O)NCC(C(=O)O)CC(=O)O
    optical_activity [α]20/D +19° to +21° (c=1, H2O)
    melting_point 133-137°C

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

    Packing & Storage
    Packing Cbz-L-Glu-OH is supplied in a sealed amber glass bottle, 5 grams, labeled with product details, hazard warnings, and batch information.
    Shipping Cbz-L-Glu-OH is shipped in tightly sealed containers to prevent moisture and contamination. It is packed according to standard regulations for chemical goods, typically in cool, dry conditions with appropriate labeling. Shipping documentation includes safety data sheets, and handling precautions are emphasized to ensure safe transit and compliance with transport regulations.
    Storage Cbz-L-Glu-OH (N-Cbz-L-glutamic acid) should be stored in a cool, dry place, protected from light and moisture. It is recommended to keep the container tightly closed when not in use and store at 2–8°C (refrigerator). Ensure proper labeling and avoid exposure to incompatible substances. Follow standard laboratory safety and storage protocols for chemicals.
    Application of Cbz-L-Glu-OH

    Applications of Cbz-L-Glu-OH in Industrial Manufacturing

    Cbz-L-Glu-OH serves as a pivotal protected amino acid intermediate in multiple advanced industrial sectors. The following sections summarize major downstream segments where manufacturers integrate this material for precise synthetic requirements, emphasizing regulatory alignment, formulation practices, process placement, and resulting end products.

    1. Peptide Active Pharmaceutical Ingredient (API) Synthesis

    Pharmaceutical manufacturers utilize Cbz-L-Glu-OH as a protected glutamic acid building block during solid-phase and solution-phase peptide synthesis processes. Its use facilitates selective peptide chain elongation, particularly in sequences where glutamate residues require controlled deprotection and coupling. The compound’s carbobenzoxy group remains stable under standard coupling conditions, enabling precise control over the integrity of side-chain functionalities throughout multistep synthesis. Suitable for peptides applied in therapeutic biologics, hormones, and research compounds, this raw material underpins the consistency and safety of regulated peptide APIs.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredient Manufacturing
    • EU EudraLex Volume 4 GMP for APIs
    • U.S. FDA 21 CFR Part 210/211 and Part 314
    • European Pharmacopoeia monographs for amino acid derivatives

    Typical usage ratio

    • 10–35 mol% relative to target peptide sequence; quantity depends on peptide length, sequence, and process scale-up.

    Downstream process integration

    • Introduced after resin linkage in SPPS as a protected glutamate source for C- or N-terminal insertion.
    • Deprotection and cleavage step under controlled conditions post-chain assembly.
    • Integrated with coupling reagents (HBTU, DIC, etc.) and compatible resins (Wang, Rink amide).
    • QC-tested for residual solvents and enantiomeric purity before final API release.

    Final product types

    • Peptide drug APIs (e.g., exenatide, leuprorelin, glatiramer acetate)
    • Custom peptide reagents for clinical research
    • Reference standards for regulated release formulations
    • Diagnostic test peptides used in medical devices

    2. Peptide-Based Cosmetic Ingredient Production

    Specialty cosmetics manufacturers employ Cbz-L-Glu-OH in the synthesis of functional peptides, particularly those incorporated into anti-aging, skin-brightening, and anti-wrinkle formulations. The protected acid form ensures selective condensation with other amino acids, preserving reactivity and sequence fidelity. After assembly and deprotection, the resulting peptides are incorporated into cream bases, serum vehicles, and surface delivery systems. This ensures batch-to-batch consistency and compliance with international cosmetic ingredient registries and safety assessment protocols.

    Industry compliance standards

    • ISO 22716 Cosmetics GMP Guidelines
    • EU Regulation (EC) No 1223/2009 for cosmetic ingredients
    • Cosmetic Ingredient Review (CIR) safety assessment principles
    • INCI registration requirements for functional peptides

    Typical usage ratio

    • 5–20 mol% of total amino acid content per peptide batch; adjusted based on peptide length and target biological activity.

    Downstream process integration

    • Solubilized and coupled during the protected assembly stage of cosmetic peptide synthesis.
    • Protective group removal after sequence completion under mild acid or catalytic hydrogenation.
    • Purified and filtered prior to formulation blending.
    • Subjected to allergen and cytotoxicity screening before market launch.

    Final product types

    • Signal peptides for topical anti-aging serums
    • Whitening and skin barrier–supporting peptide actives
    • Peptide-enriched facial masks and emulsions
    • Functionalized peptide solutions for cosmeceuticals

    3. Custom Research Peptide Synthesis for Biotech and Academia

    Research labs, biotech startups, and contract research organizations integrate Cbz-L-Glu-OH as a protected precursor in the production of designer peptides required for antibody generation, structure-activity relationship (SAR) studies, and molecular probe development. The compound’s stable carbobenzoxy group allows for orthogonal protection strategies, supporting the assembly of non-standard and isotopically labeled sequences. Its consistent reactivity reduces batch variability in research-scale syntheses, which is critical for analytical reproducibility and peer-reviewed publication requirements.

    Industry compliance standards

    • GLP (Good Laboratory Practice) for regulated research peptides
    • ISO 9001:2015 quality management systems for R&D facilities
    • NIH and EU Horizon 2020 research funding compliance
    • Institutional Material Transfer Agreement (MTA) for peptide distribution

    Typical usage ratio

    • 10–25 mol% per synthesized peptide chain; adjusted by project scope and research scale (milligram to gram).

    Downstream process integration

    • Loaded at the protected amino acid addition stage during manual or automated synthesis runs.
    • Deprotected immediately before cleavage or left intact for further modification.
    • Purified by preparative HPLC or FPLC depending on downstream use.
    • Tested for sequence verification by mass spectrometry and amino acid analysis.

    Final product types

    • Custom peptide antigens for antibody development
    • Labeled peptides for receptor binding assays
    • Peptidomimetics for molecular modeling and SAR
    • Synthetic standards for enzyme activity measurements

    4. Intermediate for API Manufacturing in Protected Glutamic Acid Derivative Processes

    Proprietary pharmaceutical and fine chemical manufacturers rely on this protected amino acid as a selective intermediate in multi-stage syntheses of small molecules and complex APIs where specific glutamate-derived side chains serve as key structural motifs. The material’s protective group reduces unwanted side-chain reactions, improving yields and reducing costly impurities. Its use benefits processes requiring stringent impurity profiles, such as asymmetric hydrogenation, amide coupling, or as a substrate for chiral auxiliaries in later-stage transformations.

    Industry compliance standards

    • U.S. FDA cGMP for registered intermediate production
    • ICH Q3A Impurities in New Drug Substances
    • Japanese Pharmacopoeia for synthetic intermediates
    • USP General Chapter <1116> for critical cleanroom operations

    Typical usage ratio

    • 5–30 mol% per batch depending on molecular complexity, downstream conversion rates, and campaign process requirements.

    Downstream process integration

    • Added post-activation in amide coupling or esterification reactions for intermediate formation.
    • Protective group removal and subsequent conversion to target intermediates for final API synthesis.
    • Processed under controlled, validated conditions to control batch impurities and chiral integrity.
    • Typically staged as a mid-process control point for QC sampling.

    Final product types

    • Protected peptide intermediates for on-patent APIs
    • Key intermediates for neuroactive drugs
    • Custom amino acid derivatives for commercial scale-up
    • Fine chemicals for advanced medicinal chemistry
    Free Quote

    Competitive Cbz-L-Glu-OH prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.

    We will respond to you as soon as possible.

    Tel: +8615371019725

    Email: admin@sinochem-nanjing.com

    Get Free Quote of Sinochem Nanjing Corporation

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Introducing Cbz-L-Glu-OH: Insights from the Manufacturing Floor

    What Sets Cbz-L-Glu-OH Apart

    Every batch of Cbz-L-Glu-OH leaving our facility reflects years spent refining both process and product insight. In this plant, we've focused on clean protection and stable delivery for L-glutamic acid derivatives, preferred by research labs and peptide synthesis operations worldwide. The backbone of Cbz-L-Glu-OH—more formally known as N-Cbz-L-Glutamic acid—shows up consistently in peptide chemistry for a simple reason: reliable N-terminal protection with the benzyloxycarbonyl group stays intact where other options fail.

    We measure value in purity levels you can track on chromatograms, not just in promises. Over hundreds of production runs, our team follows a clear path: exact pH control, slow and careful temperature ramps, and resin filtration that removes particulates from the finished product. Our raw materials come in with certificates and spectral data, but it’s the in-house HPLC testing that calls the final shot—above 99% purity or the batch gets thrown back into reprocessing.

    Up close, the difference is tangible. Cbz-L-Glu-OH comes as a crystalline solid, but long-handled scoops show the difference between a dry flow and sticky intermediates. For manufacturing, that means easier handling and less mess during transfer. Proper crystallization control reduces fine dust, which matters for both yield and operator comfort.

    Model and Specifications: Lessons from the Lab

    Through real runs, we settled on a product form that keeps things straightforward. Cbz-L-Glu-OH, our Model: CBG025, presents as an off-white powder with no sharp odor and a melting point typically clocking in around 140-144°C. Packaging choices shape the user’s day as much as the chemistry itself, so we worked with end-users to find the right texture and particle size. Too fine and it puddles at interfaces, too coarse and it clogs the scoops. Batch QC envelopes always show moisture content and specific rotation, confirming both purity and chirality—because one slip in stereochemistry sours an entire synthesis.

    End-users often want to know about solubility and storage. We store finished lots under nitrogen, in sealed containers, to prevent moisture pickup and oxidative discoloration. Cbz-L-Glu-OH dissolves well in DMF, DMSO, and dilute alkaline solutions; we avoid direct aqueous dissolving to preserve the integrity of the carbamate group. For long-term stability, we routinely check for trace decomposition, using successive batches as internal controls for shelf-life comparisons.

    Practical Use: Facing the Synthesis Bench

    Years ago, peptide coupling with unprotected L-glutamic acid meant side reactions and cleanup headaches. Adding the carbobenzoxy (Cbz) group at the N-terminus turned that scene around. In peptide chains, Cbz-L-Glu-OH keeps the amine protected through alkali and acid steps, then releases cleanly under hydrogenolysis. The choice between Cbz and other protecting groups—FMOC, Boc—tends to boil down to process needs and available deprotection equipment. Unlike FMOC, which demands a base-cleavage step, Cbz allows deprotection by catalytic hydrogenation, fitting nicely into workflows relying on Pd/C setups.

    We watch our product feed into both solution-phase peptide synthesis and the SPPS (solid-phase peptide synthesis) routes. Researchers often comment on reactivity and side product suppression. Cbz-L-Glu-OH helps prevent cyclization and incorrect condensation, thanks to the protected alpha-amino site and carboxylic acid free for activation. In automated peptide synthesizers, batch-to-batch consistency reduces calibration headaches.

    Outside classic peptides, Cbz-L-Glu-OH steps into enzyme substrate design, especially when chemists need controlled modification at the γ-carboxyl group. Our experience working with specialty pharma outfits taught us that subtle variations in crystalline habit can make or break downstream esterification. That's why we keep particle profiles and XRD (X-ray diffraction) data on every lot—the difference may seem academic, but changes in crystal faces affect slurry mixing and filtering times.

    Comparisons with Other Variants

    Cbz-L-Glu-OH often faces off against Fmoc-L-Glu-OH and Boc-L-Glu-OH. The chemical roots stay constant—these are all N-protected forms of L-glutamic acid—but the protecting group changes both the way the product behaves and the circumstances in which it’s used. Fmoc handles fast base-mediated cleavage and sees a lot of action in high-throughput peptidomimetic labs. Boc gives an acid-labile group, better for acidolysis but less robust to certain process steps. Cbz offers time-tested thermal stability and a gentle deprotection path, minimizing risk during purification.

    As a manufacturer, we've seen requests shift based on both regulatory landscape and end-process equipment. European and Japanese buyers lean toward Cbz-protected materials, relying on legacy GMP campaigns with established Pd/C hydrogenolysis equipment. North American peptide startups often ask for FMOC-protected materials for faster bench work and automated platforms. Cbz-L-Glu-OH holds its ground for any process preferring hydrogenolytic deprotection and old-school reliability.

    Costs reveal subtle tradeoffs. Cbz-L-Glu-OH pulls raw material pricing from well-established supply chains, so cost swings stay moderate even as solvents or Pd/C prices edge up. More exotic variants like Alloc-L-Glu-OH or Trt-L-Glu-OH bring higher cost and volatility because niche intermediates remain harder to source on demand. Fmoc- and Boc-protected materials sometimes cost less at scale, but pay for it in the complexity of handling waste streams with different deprotection byproducts.

    Consistency and Quality: Earning Trust in the Industry

    Long relationships with customers don’t rest on luck. Every kilo shipped with our logo means in-house analytics, not just reliance on supplier paperwork. Our Cbz-L-Glu-OH batches run through HPLC and NMR screening before certification, so we avoid any discussion about unidentified peaks or ambiguous optical purity. Tracking each lot creates a paper trail through our system—every deviation flagged for full investigation, with process notes appended for future runs. If a batch looks different in the drum—color, clumping, or spectral profile—we pull it offline and dissect the root cause.

    Inbound inspections of raw L-glutamic acid and Cbz-chloride make for smoother production. We require both FTIR and melting point checks before those materials reach the reactor, saving time and reducing waste when intermediates don’t meet spec. Building up a stock of reliable suppliers means we rarely scramble at the last minute, and customers see the steady quality in their delivered product. For users in regulated fields—GMP peptides, biotech research, and early-stage pharma—this kind of traceability often makes approval easier.

    Over the past five years, we've responded to process deviations by tightening our standard operating procedures. Temperature mapping, agitation speed logging, and in-process titration prevent surprises. On the human side, hands-on training and cross-checks among production staff reduce skipped steps and overlooked signals. Product recalls and reworks devastate trust, so we treat each Cbz-L-Glu-OH batch as both a chemical and a reputation line item.

    Sustainability, Safety, and Responsible Practices

    Production of Cbz-L-Glu-OH must strike a balance—quality output, safety for operators, and real effort to minimize waste. Our plant moved away from high-volume chlorinated solvents a decade ago, favoring greener options wherever feasible. Carbon recovery units trap benzyloxycarbonyl byproducts, cutting down atmospheric emissions and letting us recycle a portion of reagents. Wastewater streams get neutralized and filtered to strict limits before discharge.

    Operator safety builds into every step. The process brings in Cbz-chloride, with all the corrosiveness and volatility that entails, so we use contained charging and venting lines. Automated mixing minimizes direct exposure, and air-handling systems extract vapors at the source. Finished product handling follows similar caution—dry, dust-free environments, gloves and goggles, regular health surveillance for staff. Incident reviews guide equipment upgrades and safety protocol revisions, pushing us to protect both workers and customers.

    End users sometimes worry about trace residuals from heavy metals or solvents. All our Cbz-L-Glu-OH batches pass thorough analytics for residual Pd, chlorides, and organic traces. Our own QC walks the line between regulatory compliance and the higher bar often set by our largest customers, especially those in the pharmaceutical or food additive space.

    Challenges and Solutions: Up Close with Cbz-L-Glu-OH Production

    No manufacturing process runs free of hurdles, and Cbz-L-Glu-OH offers its share. The carbobenzoxy installation step sometimes generates off-odors and heat, raising the risk of byproduct formation if pH and cooling get neglected. We’ve had to develop staged addition protocols, slow feed rates, and segmented feeds of Cbz-chloride to tame those exotherms. On the back end, filtration becomes challenging as product grain size changes with cooling profile; finer product holds more filtrate and can drive up dry time.

    Product purity doesn’t only rely on the main reaction. Minor impurities crop up from residual starting materials, incomplete benzyloxycarbonylation, or side chain overprotection. Each presents a cleanup puzzle—either take the time in reprocessing or adopt new purification techniques. Through process improvements and real analysis of problem batches, we've minimized customer complaints related to spotty purity or solubility.

    Weather, supply chain kinks, and broader raw material pricing shifts always threaten to disrupt schedules. In response, we built contingency stocks and added local pre-processing for core inputs. This allows us to hedge against both transportation lags and unexpected customs delays, ensuring our partners receive material on schedule.

    Direct Feedback: Listening to Chemists, Not Only Sales

    Much of what we changed in Cbz-L-Glu-OH manufacturing came from the honest feedback of bench chemists and process engineers using the product every day. Some reported that static cling in fine powders slowed their work or that partial dissolution in key solvents added filtration headaches. Others noted shipment delays when supply chains stretched thin. We set up regular calls with key customers—not just sales or procurement, but the users running actual reactions. Their input led to tweaks in crystal definition, anti-caking agents, and even carton sizing. These changes paid dividends as complaint rates dropped and reordering intervals shrank.

    One memorable call came from a peptide lab head, pointing out subtle color shifts in a late winter batch—the result, it turned out, of a temporary change in cooling water temperature. That anecdote stuck with our team, becoming a trigger for installing tighter temperature control and real-time monitoring. Experience on both sides, from plant to bench, means constant improvement for Cbz-L-Glu-OH.

    The Road Ahead: Innovation Built on Solid Practice

    Demand for Cbz-L-Glu-OH continues to evolve as peptide therapeutics, enzyme kits, and composite materials gain traction in global research. Manufacturing doesn’t mean simply repeating the past; we invest in analytical upgrades and enhanced operator training to keep pace with newer expectations. Application trends flow back into our development cycle—interest in chromatography-grade or micronized forms sparked trials in alternative drying and milling methods. We pair that with outreach to research partners, gathering early data on new process flows.

    Digitization, once a buzzword, now shapes our routine QC and record-keeping. Automated sampling and direct-to-database uploads allow us to spot long-term drift across hundreds of Cbz-L-Glu-OH batches. Review meetings comb through data sets not just for compliance, but for areas where process tweaks can unlock higher reliability or smoother large-scale output.

    Global regulation presents both constraint and opportunity. Compliance with emerging requirements—REACH in the EU, FDA guidelines in the US, evolving standards in Asia—means we stay agile, prepared to pivot or document extra details as required. By keeping research, production, and regulation aligned, we offer Cbz-L-Glu-OH not just as a chemical, but as a reliable component in the supply chain value stream.

    Conclusion: Commitment Beyond Commodity Chemistry

    Cbz-L-Glu-OH reflects the steady accumulation of lessons learned under real-world pressure—unexpected batch quirks, on-the-fly fixes, and day-to-day collaboration with users. Each decision, from raw material vetting to final packaging, comes down to balancing practical chemistry with user focus. We don’t treat this product as just another list entry or catalog number; for us, it’s the result of thousands of hours of labor, documentation, and teamwork.

    Those seeking Cbz-L-Glu-OH partner with a team committed to the details, ready to answer technical questions and adapt to fresh process demands. We stand by our approach—tight controls, open dialogue with end users, and a willingness to revisit and refine every element of production. As new fields open and applications diversify, our mission remains the same: to deliver Cbz-L-Glu-OH with consistent quality, supported by real experience from the manufacturing floor.