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N-Carbobenzoxy-Dl-Serine

    • Product Name N-Carbobenzoxy-Dl-Serine
    • Alias Z-DL-Serine
    • Einecs 256-886-4
    • 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
    VTB
    Specifications

    HS Code

    603400

    Product Name N-Carbobenzoxy-Dl-Serine
    Cas Number 15434-65-6
    Molecular Formula C10H11NO5
    Molecular Weight 225.20
    Appearance White to off-white powder
    Purity Typically ≥98%
    Melting Point 128-130°C
    Solubility Slightly soluble in water, soluble in methanol and ethanol
    Storage Temperature 2-8°C
    Synonyms Z-DL-Serine, Benzyloxycarbonyl-DL-serine
    Structural Formula C6H5CH2OCO-NH-CH(COOH)-CH2OH
    Use Peptide synthesis intermediate
    Inchi InChI=1S/C10H11NO5/c12-7(13)6-8(14)11-10(15-9-4-2-1-3-5-9)16-11/h1-5,8,14H,6H2,(H,12,13)
    Smiles C1=CC=C(C=C1)COC(=O)N[C@@H](CO)C(=O)O
    Ec Number 239-446-3

    As an accredited N-Carbobenzoxy-Dl-Serine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, sealed plastic bottle labeled "N-Carbobenzoxy-Dl-Serine, 25g." Features safety symbols, lot number, and storage instructions.
    Shipping N-Carbobenzoxy-Dl-Serine is shipped in tightly sealed containers, protected from moisture and light, and handled in accordance with standard chemical safety protocols. The shipment is labeled with appropriate hazard information and transported under controlled conditions to prevent degradation or contamination, ensuring safe and compliant delivery to the receiving laboratory or facility.
    Storage N-Carbobenzoxy-Dl-Serine should be stored in a tightly closed container, protected from light and moisture. It should be kept at 2-8°C (refrigerated conditions). Ensure storage in a well-ventilated, cool, and dry area, away from incompatible substances such as strong oxidizers. Properly label the container and minimize exposure to air to maintain chemical stability.
    Application of N-Carbobenzoxy-Dl-Serine

    Applications of N-Carbobenzoxy-Dl-Serine in Industrial Manufacturing

    N-Carbobenzoxy-Dl-Serine serves as a protected serine derivative, widely utilized in highly regulated synthesis environments. We manufacture this material with strict process control, addressing diverse needs across pharmaceutical, peptide, specialty chemicals, and research reagent production.

    1. Peptide Synthesis Intermediates

    Pharmaceutical and biotechnological companies use N-Carbobenzoxy-Dl-Serine as an intermediate for assembling protected oligopeptides by solution-phase and solid-phase synthesis. The carbobenzoxy (Cbz) group provides temporary amino protection during peptide elongation. Industrial peptide synthesis lines employ this raw material in scale-controlled reactors. Operators precisely deprotect the Cbz group at targeted synthesis steps, enabling accurate sequence assembly. Manufacturers perform comprehensive in-process analysis to ensure residue removal, minimizing impurity carryovers. Quality control teams verify lot conformity to minimize batch deviations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) guidelines for active pharmaceutical ingredient (API) intermediates
    • USP General Chapter 1045 on Biotechnology-Derived Articles
    • ISO 9001:2015 Quality Management Systems
    • Ph. Eur. 2034 and JP XVII monographs (where applicable for downstream APIs)

    Typical usage ratio

    • 0.2–1.5 molar equivalents per peptide coupling step, adjusted by peptide length and side chain requirements

    Downstream process integration

    • Used after initial resin loading or prior to intermediate coupling reactions
    • Undergoes deprotection by catalytic hydrogenolysis or acidolysis, depending on process route
    • QC monitoring for residual protecting groups and side products

    Final product types

    • Pharmaceutical-grade synthetic peptides
    • Research peptide APIs for small-molecule drugs
    • Custom diagnostic peptide reagents
    • Peptide reference standards

    2. Chiral Auxiliary Production

    Manufacturers employ N-Carbobenzoxy-Dl-Serine as a precursor in the synthesis of chiral auxiliaries for asymmetric organic reactions. The serine backbone provides a stereochemical handle for resolving racemic mixtures, while the benzyl protection maintains process integrity until selective removal. Industrial users maintain tight reaction temperature and pH control during auxiliary formation, integrating dedicated purification and crystallization units to obtain enantiomerically enriched auxiliaries. On-site analytics confirm chiral purity and batch identity before distribution to fine chemical manufacturers.

    Industry compliance standards

    • ISO 9001:2015 for specialty chemical production
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU Regulation)
    • Appropriate handling protocols for controlled intermediates

    Typical usage ratio

    • 1.0 mol equivalent per auxiliary batch; final ratio varies by target chiral auxiliary and subsequent derivatization

    Downstream process integration

    • Intake post-initial condensation/separation step
    • Further modified via esterification or amidation to generate specific chiral auxiliaries
    • Purification typically by column chromatography or fractional crystallization

    Final product types

    • Custom chiral auxiliaries for asymmetric catalysis
    • Resolution agents for enantiopure pharmaceutical synthesis
    • Chiral building blocks for advanced intermediates

    3. API Intermediate Synthesis in Small Molecule Drugs

    Facilities specializing in small-molecule drug synthesis integrate N-Carbobenzoxy-Dl-Serine as an intermediate for CNS agents and anti-infectives. Formulation teams design multi-step synthesis schemes where this building block supports selective transformation, such as nucleophilic substitution or amidation. Operators utilize dedicated hydrogenolysis equipment to remove the Cbz group post-coupling, ensuring no protecting group contamination in downstream API synthesis. Quality assurance tracks each lot for impurity profiles and consistent molecular integrity under cGMP environments.

    Industry compliance standards

    • 21 CFR Part 211 (FDA cGMP for Drugs)
    • ICH Q3A Impurities in New Drug Substances
    • China Pharmacopoeia (ChP) for API intermediates

    Typical usage ratio

    • 0.3–1.0 molar ratio as dictated by target molecule and desired yield; optimized through route scouting

    Downstream process integration

    • Used in early- and mid-stage reaction cascades before key structure-forming steps
    • Cbz protection provides selectivity during functional group transformations
    • Removal of the Cbz group just prior to final API coupling steps

    Final product types

    • Active pharmaceutical ingredients for CNS drugs
    • Antibacterial and antiviral drug intermediates
    • Synthetic routes for amino acid-based drug candidates

    4. Research and Development Reference Material

    Universities and industrial research institutions regularly source N-Carbobenzoxy-Dl-Serine as a research-grade reference material. Analytical chemistry and medicinal chemistry groups use the compound for method validation and as a calibration standard for HPLC, NMR, and mass spectrometry. Laboratories require highly characterized lots free of related amino acid impurities and documented traceability from GMP-compliant production records. Material safety and precise documentation remain necessary for institutional reviews and internal approvals.

    Industry compliance standards

    • ISO/IEC 17025 for laboratory reference materials
    • GLP (Good Laboratory Practice, OECD Principles)
    • Detailed certificate of analysis (CoA) for traceability

    Typical usage ratio

    • Microgram to gram quantities per experiment, depends on calibration sensitivity needs and detection limit requirements

    Downstream process integration

    • Dissolved in analytical-grade solvents for calibration and QC assays
    • Benchmark for method development in peptide and small molecule research
    • Supports equipment qualification (IQ/OQ/PQ)

    Final product types

    • Analytical calibrants for HPLC or LC-MS
    • Reference standards for publication or method validation
    • Internal laboratory control samples
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    Certification & Compliance
    More Introduction

    N-Carbobenzoxy-Dl-Serine: Experience From the Manufacturer’s Bench

    Understanding Our Approach to Amino Acid Building Blocks

    At our manufacturing site, years of hands-on experience shaping fine chemicals and amino acid derivatives frame the choices we make. N-Carbobenzoxy-Dl-Serine plays a measurable role in peptide synthesis and research, a contribution that deserves both practical knowledge and honest discussion. We recognize that chemists rely on clean, predictable building blocks to build more complex structures or to screen new candidates for drug leads and bioactive compounds. Every gram shipped reflects months—sometimes years—honing reactions, workflows, and purification routines.

    What N-Carbobenzoxy-Dl-Serine Offers

    We manufacture N-Carbobenzoxy-Dl-Serine using a batch production system, maintaining full traceability back through raw materials and each process stage. The structure—N-[benzyloxycarbonyl]-Dl-serine—brings an N-terminal protection (carbobenzoxy, or Cbz) to a mixture of both serine enantiomers. The DL-grade gives researchers or peptide technologists flexibility, often at a lower price-point than strictly enantiopure (L- or D-) material. This makes it attractive for methods development, reaction evaluation, or when chirality control returns elsewhere in a synthesis route.

    We achieve a purity threshold that matches most published protocols for peptide intermediates, verified batch-by-batch by HPLC, melting point, and NMR data. By using raw serine of high grade and a dedicated carbobenzoxy protection protocol, we narrow down sources of side-products—an issue that matters where protecting group stability and ease of later deprotection are pivotal.

    Standard packaging options align with scale and storage needs. Several customers order in hundreds of grams, planning campaigns of solid-phase peptide synthesis, while some require kilograms where cost curves matter more than margins on smaller lots. Our processes have proven reliable for research up through semi-pilot scale, making route transfer smooth for those moving from bench to larger reactors.

    The Real Differences of Dl-Grade: Use Cases and Advantages

    Compared to enantiomerically pure N-Carbobenzoxy-L-serine, the DL version mixes both mirror-image forms of the serine sidechain. To many outside organic chemistry, this might sound like a shortcut, but there’s a logic behind it. Certain combinatorial libraries and screen compounds deliberately use racemic precursors. The savings in production and the wider guarantee of encompassing both biological configurations deliver quicker answers in structure-activity studies.

    We often see technical teams ask for the DL grade when budgets steer project timelines and reports focus on process answers rather than final product. Because we run both pure and racemic lines, we have seen DL products feed into broader chemical routes—heterocycle development, protected building blocks for ligation, and epoxide ring-openings—cases where later downstream selection or resolution sorts out the preferred isomer.

    The N-protecting group doesn’t just shield the functional group during multi-step reactions. Cbz protection allows selective deprotection under mild hydrogenolysis, a fact our repeat customers point out whenever projects rely on flexibility. The slight bump in molecular weight from the benzyloxycarbonyl group, and its relative bulk, sometimes influences solubility or partitioning in extraction protocols, so our experience flags this for customers designing new stepwise syntheses.

    From Raw Material to Final Compound: An In-Depth View

    Authentic chemical manufacturing draws strength from years spent refining each step, rather than sourcing intermediates elsewhere and blending for resale. We handle both serine resolution and Cbz-protection in-house, using reagents with proven performance and supply continuity. Our purification uses column chromatography and repeated crystallizations, honed by quality audits and direct feedback from process engineers.

    The presence of both D- and L- configurations in our DL batch means less complexity for certain applications and more for others. Selective use of this racemic material enables high-throughput screening at lower total input cost, but researchers focused on single-isomer peptides may prefer other lines from our portfolio. We remain transparent on source, enantiomeric content, and analytical confirmation—never hydrolyzing pure L-serine to increase apparent DL yield. For formulations, we provide data showing each lot’s typical appearance, moisture content, and residual solvent profile, so those in regulated settings receive predictable product.

    How the Choice of Protecting Group Influences Synthesis

    Cbz stands out among N-protecting groups for serine derivatives thanks to a blend of stability and ease of deprotection. Over time, many chemists have compared it with Fmoc or Boc alternatives. Our experience suggests that Cbz’s hydrogenolysis removal pathway proves most forgiving under a range of conditions, especially where catalytic loads or solvent choices constrain a project’s economics or safety. Working with hydrogen, charcoal, and palladium in reactors that meet our in-house safety standards, our team routinely achieves clean removal, freeing the primary amine without over-reduction or racemization.

    Yield shouldn’t come at the cost of purity. During scale-up, we pay special attention to potential side-products: N,O-dibenzylated compounds, benzyl carbamate hydrolysis fragments, or oxidized byproducts that may elude less vigilant producers. We engage directly with users to modify crystallization habits when a particular downstream impurity profile proves stubborn. NMR spectra and HPLC chromatograms from our central quality lab keep surprises to a minimum.

    Product Handling Lessons From Daily Manufacturing Reality

    Whether packaging 25-gram vials or assembling pails of multi-kilogram lots, our warehouse team stays vigilant about moisture pick-up, static charge, and shipping stability. The white to off-white crystalline powder responds quickly to humid air, so each batch leaves our doors vacuum-sealed and double-bagged if the trip crosses long supply routes. Feedback loops with our logistics and technical sales teams bring reports from the field: what held up in storage, what clumped in hot summer months, and what dissolved easily in lab buffers.

    We help customers set up their own handling protocols on site. Desiccators, inert-atmosphere glove boxes, or simple bottle sealing—a dozen tweaks that keep product fresh through weeks of research, not hours. Part of the value comes from our willingness to discuss shelf-life openly; we don’t oversell the stability window, preferring to win long-term respect over quick sales.

    Supporting Research Goals: Connecting Directly With Users

    We seek out honest conversations with those using our material, whether in university peptide labs, hospital research cores, or industrial screening teams. Our technical staff keeps records of synthetic bottlenecks relayed from end-users: where N-Carbobenzoxy-Dl-Serine performed as planned and, equally, where a purification step posed an unexpected challenge. If a customer’s hydrogenolysis setup required longer reaction times or generated micrograms of benzyl alcohol, we add that detail to our troubleshooting notes.

    Collaboration extends to custom order requests. We have processed dozens of batches at nonstandard concentrations, particle size specifications, or with tailored analytical support. This attitude doesn’t just improve product—it keeps our understanding rooted in real-world chemistry and builds trust beyond emails and catalog lists.

    Comparing to Other Protected Serine Derivatives

    As pure manufacturers, we compare our product straight to other protected serines on the market: N-Boc, N-Fmoc, unprotected, or those with alternative O-protection like t-butyl groups. Each serves its place. Boc offers removable acid lability but less versatility in downstream solid-phase peptide work, where Cbz shines. Fmoc-protected materials dominate certain segments of automated peptide synthesis due to compatibility with base-labile protocols, but their price and handling quirks can slow smaller labs.

    Our throughput and documentation reflect a deliberate focus on Cbz chemistry. We base this on direct tally of customer preferences and historic success in deprotection reliability. Multiple years of batch production demonstrate that users can develop and debug their methods faster with a material that uncovers fewer surprises. Where others focus on sourcing, we keep our technical staff trained on reaction trends, emerging literature, and user-reported side reactions.

    Lessons From Manufacturing Scale-Up

    Scaling up protected amino acids exposes differences invisible at the bench. Our staff—most of whom trained on small glass reactors—work side by side with those responsible for stainless steel vessels, jacketed crystallizers, and filtration assemblies. Transitioning from 25-gram to 2-kilogram runs required careful recalibration. Reproducibility hinges not only on stoichiometry but on solvents’ age, catalyst lots, and the timing of quenching and work-up.

    We solved bottlenecks more than once by stepping through the process. Our team once traced nickel contamination back to an overlooked support bracket in a filter press; after months of troubleshooting, this became a cautionary tale shared at every onboarding. Solvent recycling helped us tighten cost and supply security, but it also forced us to sharpen analytical tests for every cycle. We learned that robust quality control doesn’t just serve customers, it prevents costly rework.

    Addressing Safety and Environmental Expectations

    Chemical manufacturing nowadays draws more scrutiny than in years past. We manage waste streams, hydrogen handling, and solvent storage with greater rigor—using double-walled tanks, air monitoring, and trained shift rotations. A product like N-Carbobenzoxy-Dl-Serine brings legacy catalyst residues, and we set our internal standards tighter than customary regulations. Our choice of solvents and reagents balances worker safety, product quality, and waste minimization.

    On the environmental side, we process and neutralize hydrogenation off-gas and recover as much solvent as practical for reuse. Our relationships with upstream suppliers factor in both traceability and hazardous material certifications, ensuring the raw serine comes from sources meeting accepted food or pharma grades. Most of this never shows up in a catalog description, but it defines the real difference between simply trading a chemical and making it responsibly.

    Challenges in Documentation and Regulatory Support

    More regulatory documentation requests reach us every year, often for filings related to clinical peptide work or as part of supplier qualification for regulated industries. We respond not with templated product summaries, but with direct access to batch records, impurity profiles, and sometimes method validation results.

    We’ve learned that written assurances only go so far—backed data, trend charts, and real certificates bring customer confidence. Analytical development sits in the same hallway as production; close proximity helps interpretation when the inevitable “why is my HPLC baseline drifting?” query arises. We don’t hide process changes—each change control packs a paper trail and, for many long-term customers, a direct phone call.

    Building Trust Over Years of Manufacture

    Decades in this field taught us that each batch is part of a wider web of research and manufacturing. Some customers modify N-Carbobenzoxy-Dl-Serine once, then move on; others circle back every cycle, reporting successes and setbacks. We track performance statistically from each customer feedback, making operational tweaks or, sometimes, developing entire new purification trains.

    Unlike distributors, we do not pivot supply based solely on price. Our process remains visible—site inspections stand open, quality and technical managers ready to discuss granular details or walk a new partner through our paperwork. We earn repeat business less from upfront cost than from a helpline that stays open and staff who actually blend, filter, and pack these materials.

    The Road Ahead for N-Carbobenzoxy-Dl-Serine

    Product lines evolve; so do user expectations. Peptide therapeutics and biologics continue demanding higher traceability, stricter analytical data, and shorter turnaround times. Open discussion with research partners guides future investments, whether that means scaling reactor capacity or developing variant protection schemes for new classes of amino acids.

    By owning the process from raw material receipt to packed product leaving our warehouse, we offer something that resellers can only glimpse: hard-won familiarity with each batch, a working understanding of both limits and triumphs in protected amino acid chemistry. Those who use N-Carbobenzoxy-Dl-Serine know the difference a dedicated manufacturer brings—measured not just in COA paperwork, but in every gram weighed, blended, and checked, time after time.

    Bringing Reliability to the Bench and Pilot Plant

    Over years, we have established connections with synthetic chemists, method developers, formulation teams, and regulatory affairs officers. We listen, revise, and, when necessary, challenge assumptions—building the kind of material consistency that doesn’t rely on luck. We don’t claim perfection, but we do make improvements batch after batch, incorporating each experience into the next.

    Material like N-Carbobenzoxy-Dl-Serine might not claim the limelight, but for those building new peptides, biologically active libraries, or technical routes where reliability counts, it delivers consistent performance. Direct engagement, transparent practices, and a process that values quality over convenience remain our approach. This builds not only products, but relationships that support discovery, scale-up, and, ultimately, innovation across the fields that rely on protected amino acids.