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O-Benzyl-(D)-Serine Benzyl Ester

    • Product Name O-Benzyl-(D)-Serine Benzyl Ester
    • Alias Bz-Ser-OBzl
    • Einecs 691-933-0
    • 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
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    Specifications

    HS Code

    770958

    Product Name O-Benzyl-(D)-Serine Benzyl Ester
    Molecular Formula C16H17NO3
    Molecular Weight 271.32 g/mol
    Cas Number 27419-37-8
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in organic solvents (e.g., dichloromethane, methanol)
    Melting Point 58-62°C
    Optical Rotation +15° to +20° (c=1, MeOH)
    Storage Conditions Store at 2-8°C, protected from light and moisture

    As an accredited O-Benzyl-(D)-Serine Benzyl Ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing O-Benzyl-(D)-Serine Benzyl Ester, 5 grams, is packaged in a sealed amber glass bottle with tamper-evident cap and labeling.
    Shipping O-Benzyl-(D)-Serine Benzyl Ester is shipped in tightly sealed containers, protected from moisture and light. It is packed according to standard safety protocols for shipping chemicals, including cushioning to prevent breakage. Transport is conducted under ambient conditions, with all relevant safety documents and labeling to ensure compliance with chemical shipping regulations.
    Storage O-Benzyl-(D)-Serine Benzyl Ester should be stored in a tightly sealed container, protected from moisture and light, in a cool, dry, and well-ventilated area. Ideally, it should be kept at 2-8°C (refrigerator temperature). Ensure the chemical is stored away from strong oxidizing agents, acids, and bases to maintain its stability and prevent decomposition.
    Application of O-Benzyl-(D)-Serine Benzyl Ester

    Applications of O-Benzyl-(D)-Serine Benzyl Ester in Industrial Manufacturing

    Leveraging advanced synthesis capabilities and decades of small-molecule expertise, we supply O-Benzyl-(D)-Serine Benzyl Ester for high-value verticals where protected amino acid derivatives drive unique performance, compliance, and process efficiency. Our focus addresses core segments in pharmaceutical synthesis, peptide manufacturing, chiral intermediate production, and biochemical reagent supply, always under strict adherence to the industry norms and regulatory frameworks demanded by large-scale industrial buyers.

    1. Peptide Active Pharmaceutical Ingredient (API) Synthesis

    O-Benzyl-(D)-Serine Benzyl Ester functions as a protected D-serine building block in solid-phase and solution-phase peptide synthesis, minimizing racemization and side-chain participation during elongation. Its usage directly impacts peptide purity, yield, and regulatory inspection outcomes for APIs containing D-serine motifs, a critical requirement for clinical-stage development and commercial peptide drug manufacturing. Our production protocols ensure minimum byproduct formation and reproducible protection-deprotection profiles in major synthesis pipelines.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • USP <1092> Peptide Substances
    • EDQM/CPh Eur. requirements for amino acid derivatives
    • US FDA cGMP, 21 CFR Part 210/211

    Typical usage ratio

    • 0.9–1.05 molar equivalents relative to next coupling partner; adjusted depending on resin loading and target peptide sequence to minimize overuse and side reactions

    Downstream process integration

    • Charged during amino acid activation/coupling steps in solid-phase or solution-phase peptide synthesis; benzyl group deprotected after sequence assembly via hydrogenolysis

    Final product types

    • Therapeutic peptides and oligopeptides (injectables, nasal sprays)
    • Custom peptide APIs containing D-serine segments
    • Diagnostic peptides

    2. Chiral Intermediate for Small-Molecule Drug Synthesis

    This protected D-serine ester serves as a chiral precursor for the synthesis of key intermediates in pharmaceutical actives, particularly those requiring controlled stereochemistry in β-hydroxy amino acid subunits or related drug scaffolds. Its stability under mild conditions and selective benzyl protection facilitate clean transformations essential in route scouting, process scale-up, and industrial-scale active compound production.

    Industry compliance standards

    • ICH Q11 Development and Manufacture of Drug Substances
    • GMP as stipulated by EMA Volume 4 Part II
    • ISO 9001:2015 (chemical quality management)

    Typical usage ratio

    • Stoichiometric base: 1.0–1.2 molar equivalents in asymmetric synthesis; adjusted to minimize residual starting material in downstream purification

    Downstream process integration

    • Incorporated at the stereocenter-forming step or as a masked reactant during reductive amination/hydrolysis before final salt formation or crystallization

    Final product types

    • Chiral β-hydroxy acid intermediates
    • Non-proteinogenic amino acid derivatives
    • Synthetic precursors for antivirals and anticancer agents

    3. Custom Synthesis of Specialty Peptides for Research and Diagnostics

    Analytical laboratories and diagnostic product manufacturers utilize our material as an orthogonally protected amino acid unit when preparing D-serine-containing specialty peptides or peptidomimetics. The benzyl-protected side chain and carboxylate ester provide compatibility with diverse coupling reagents and sequence assembly protocols, enabling the production of libraries and site-specifically labeled peptides for bioanalytical and imaging applications.

    Industry compliance standards

    • ISO 13485:2016 for diagnostic reagent manufacturing
    • ISO/IEC 17025 laboratory accreditation
    • REACH (EC No 1907/2006, registration of chemicals for R&D uses)

    Typical usage ratio

    • 0.95–1.10 molar equivalents based on sequence requirements; lower end for combinatorial library synthesis, upper end for single-sequence custom peptides

    Downstream process integration

    • Introduced at the amino acid addition step in automated or manual synthesis protocols; maintained protected until terminal deprotection or side-chain labeling stage

    Final product types

    • Fluorescently labeled D-serine peptides
    • Bioassay controls for neurological research
    • Synthetic standards for MS or HPLC quantitation

    4. Synthesis of Protected D-Amino Acid Building Blocks for Biochemical Reagents

    Producers of biochemical reagent kits and custom amino acid suppliers use this benzyl ester derivative as an intermediate for generating highly pure, protected D-serine derivatives. Multi-step transformations—such as partial hydrogenolysis, selective de-esterification, or N-modification—yield advanced building blocks required for high-throughput screening kits and structure-activity relationship (SAR) studies in early-stage pharmaceutical development.

    Industry compliance standards

    • ISO 9001:2015 (chemicals and reagents)
    • REACH registration for reagent applications
    • Applicable clauses from ACS Reagent Chemicals guidelines

    Typical usage ratio

    • 1.0 mol equivalent per functional group conversion step; batch-adjusted according to conversion efficiency and downstream purity targets

    Downstream process integration

    • Processed as an intermediate for sequential or selective deprotection, acylation, or isotope labeling before formulation into commercial research kits

    Final product types

    • D-serine building blocks with customizable protecting groups
    • Labeled D-serine derivatives for kinetic assays
    • Biochemical kit standards for neuroscience
    Free Quote

    Competitive O-Benzyl-(D)-Serine Benzyl Ester 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.

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    Certification & Compliance
    More Introduction

    O-Benzyl-(D)-Serine Benzyl Ester: Insights From the Synthesis Floor

    From Raw Materials to Refined Precision

    Making O-Benzyl-(D)-Serine Benzyl Ester involves more than textbook chemistry. A lot happens between sourcing high-grade D-serine and shipping the final crystalline ester out of our plant. Over the years, we’ve fine-tuned every stage of synthesis. Each batch starts with D-serine’s unmistakable chirality, which we protect during conversion with a benzyl group. That benzylation defines this molecule’s core identity and stability. In our reactors, temperature and solvent control shape the critical benzylation reaction, driving both yield and optical purity. Crude product purification isn’t an afterthought, it’s a fight against trace byproducts that could alter downstream applications.

    At the scale we operate, nothing substitutes for direct hands-on sampling during each phase. TLC plates smeared with reaction drops tell more than any spreadsheet. IR and NMR checks, run in-house by people who know what real spectra look like, separate our batches from what circulates among traders who never see the raw material or finished compound.

    Tangible Specifications Rooted in Daily Practice

    Model references for O-Benzyl-(D)-Serine Benzyl Ester usually center on the compound’s high purity, low moisture, and reproducible optical rotation. Customers typically request material with purity above 98 percent, but we often run post-purification analyses pushing that boundary. Our HPLC and chiral column results show real trends batch to batch. The ester presents as white to off-white crystalline solid, non-hygroscopic if handled right. We rely on both careful packaging and accurate melting point as markers of correct structure and stability. Minute variations in melting behavior usually mean process improvements or, occasionally, a new trace impurity that we iron out using column tweaks and wash solvents.

    Water content gets managed at every filtration and drying step. These aren’t just numbers; high moisture has spoiled more than one shipment under humid conditions. Each drum leaves our floor nitrogen flushed and vacuum-sealed for assured shelf stability. Any lingering solvent must stay well below detection, or we scrap the batch. In the plant, those small details mean wasted time or success.

    Usage Grounded in Practical Chemistry

    O-Benzyl-(D)-Serine Benzyl Ester serves as a chiral intermediate in multi-step routes, especially in pharmaceutical chemistry. Its use emerges whenever stereoselectivity matters. In hands-on synthesis, this ester offers a sturdy protected D-serine backbone that endures harsh reagents until its downstream unveiling. We’ve watched this material draw steady demand from peptide labs and small-molecule drug developers. Every order ties back to a specific route, whether it’s solid-phase peptide synthesis, N-alkylated amino acid construction, or innovative API building blocks. Production chemists appreciate that our batches don’t surprise them with unknown impurities or shifts in optical rotation—especially during scale-up.

    Early on, we learned that peptide chemists expect total predictability. If the product doesn’t dissolve cleanly or presents haze in their coupling reactions, their whole sequence could stall. We avoid those headaches during our drying and sieving routine. “Does it dissolve as you want it to?” has become a common feedback point. Skilled chemists in our plant, who have worked both at bench and in kilo labs, devote attention to this simple question. Their patience shapes every shipment.

    Why Protection Matters: Benzyl Version Versus Other Forms

    The O-benzyl protection marks this ester for routes where the serine side chain needs shielding until late-stage workups. Direct use of D-serine often succumbs to side reactions, particularly during strong-acid catalysis or metal-catalyzed coupling. The benzyl group withstands these conditions without breaking open prematurely. Some labs rely on other protection patterns—like Boc or Fmoc—but the benzyl protects both the side chain and the ester bond, allowing precise deprotection at a later step. Hydrogenolysis unlocks the parent D-serine cleanly, with minimal racemization risk.

    In our experience, requests for other O-protected serine esters occur in fine-tuned routes, generally for custom synthesis. These alternatives sometimes trade off stability for easier removal or face unpredictable shelf life when exposed to moisture or base. Our benzyl protection gives robust resistance to these pitfalls. It’s a balance of process compatibility, reaction yield, and storage stability—each one a nontrivial consideration in kilogram orders or clinical trial scale-ups.

    Reliability Through Each Step, Not Just Compliance

    Many suppliers promote “meets specification” as the endpoint. From the plant side, that mindset doesn’t account for process reproducibility or what happens when a customer runs a demanding coupling or hydrogenolysis. Our process improvements often come from real-world cases: a blocked peptide synthesis or failed purification downstream. In response, we have re-examined solvents, crystallization rates, and even the grade of glassware used in some steps. Entire shifts will scrap imperfect batches, even if numbers look fine, based on sensory cues that only years of batch experience provide. That’s how we’ve reduced variances at scale.

    We trace each lot through our plant’s records, using both electronic and paper logs. Operators leave comments—why pH drifted, when the argon flush looked odd, whether a crystallization carried over trace oiliness. Our customers feel that attention in their own yields. Failures at your bench mean hours sunk; we carry that knowledge back upstream to process tweaks.

    Understanding Demand: Connections to Pharmaceutical and Research Applications

    The rising need for O-Benzyl-(D)-Serine Benzyl Ester follows the current momentum in peptide therapeutics and chiral building blocks. Small-molecule and peptide drugs require exact stereochemistry. Missteps in setting or protecting chirality mean entire campaigns fail validation, and we see those pressures reflected in procurement cycles. Upswings in demand for protected D-serine come during both fundamental research and early-stage process development for pipeline drugs. As a manufacturer, we stay engaged with trends across multiple labs—not just pharma, but academic synthesis groups probing novel post-translational modification routes or custom oligopeptides.

    Big traders rarely see these scientific drivers up close, but for us, every customer conversation leads to changed run parameters or even new analytical checks. Sometimes development teams ask about trace metals, polymorphism, or packaging materials; other times, they want flexible shipment sizes for pilot to industrial transition. Our direct control lets us tweak output flexibly—bulk orders have special storage, small bottles take extra inspection before sealing.

    Supporting Claims With Results—Not Hype

    Years of batch production and complaint resolution have developed our approach. Changes in organoleptic properties, shifts in melting temperature, or subtle discoloration mean real risk. When a batch arrives in your lab, you want guaranteed consistency, because most downstream chemistries have little tolerance for variation. Our plant performs spot-sampling by staff who have worked both synthesis and QC roles, not just temporary inspectors. They know off-odor, dust, and subtle clumping aren’t cosmetic issues—they carry real implications.

    Every batch includes a full chromatography and mass spectrometry check before our signoff. Past mistakes have left lasting lessons. Batches that once picked up ambient moisture during a sticky summer season impacted solubility for every downstream user, so we overhauled our dessication and vacuum sealing. A single batch with trace toluene odor mirrored earlier operator error, so we altered washing protocols, added operator cross-checks, and shut down the line when even marginal solvent presence appeared.

    Making Quality Everyday Reality, Not an Abstract Concept

    Quality requires vigilance beyond regulatory minimums. Our team reviews near misses even when nobody outside our walls would ever learn of them. Many choices inside the plant reflect previous headaches encountered in both internal and customer labs. Combining real-time analytics, operator know-how, and physical checks ensures the material leaves us in best form. At the scale customers order—sometimes a few grams for a new process, sometimes several kilograms for scale-up—consistency from drum to drum affects every subsequent step in the synthesis chain.

    We handle and package O-Benzyl-(D)-Serine Benzyl Ester in controlled, humidity-managed rooms with materials that don’t interact with the compound. All weighing is performed with fresh gloves and cleaned scoops. Drum liners see only a single product, and outer containers get checked for closure integrity by staff who have worked these lines for years. These methods aren’t just SOP—they’re work habits rooted in direct experience.

    Why These Distinctions Matter in the Marketplace

    Other sources may offload products that simply meet nominal HPLC standards; we’ve tested material sold through other channels and found unexplained optical rotation drift, higher LC baseline noise, and inconsistent dryness. These discrepancies take real time and money to track down during troubleshooting. Our customers expect not just clean data, but batch-to-batch certainty. They push our analytics, ask detailed questions about raw material origins, reagent history, and test conditions. We welcome that scrutiny—it’s the only way to keep confidence high in regulated environments.

    Some competitors focus primarily on volume and price. In our experience, shortcuts in protection, purification, or packaging rarely pay off. Higher returns come from predictable, documented results, as even high-volume customers will pay more for a product that doesn’t introduce risks during GMP or pilot runs. This is where manufacturer insight—not abstract commitment—makes the difference.

    Collaborative Feedback Loops: The Path to Real Solutions

    Success requires integration between our plant and the chemists applying this material. Direct dialogue creates useful changes. Years ago, a peptide developer explained unsatisfying couplings with our earlier lots. We spent days reworking our purification, swapping columns, extending wash cycles, and sampling different crystallization points. Yields and purity responded to these hands-on tweaks. The next lot performed smoothly for that customer, and subsequent feedback guided our ongoing workflows.

    Our technical support group tracks more than requests for documentation—they flag recurring questions, alert the plant to trends, and ensure recurring concerns disappear with process improvements. Sometimes a simple observation about a product’s odor, color, or behavior in methanol triggers process overhauls that cannot be summarized by numbers alone. That’s the value of a work culture that prizes direct communication—among plant technicians, chemists, and end-users.

    Building Trust Without Shortcuts

    Making O-Benzyl-(D)-Serine Benzyl Ester every day has taught us that quality is an evolving benchmark. We never stop attending to new scientific findings or regulatory guidelines, but practical lessons from the floor and direct user feedback drive the adjustments that set our material apart. From first charge of raw D-serine, through benzylation, isolation, clean-up, and final QC signoff, we apply methods proven over dozens of campaigns.

    People say, “the proof is in the performance.” Our standards reflect both hard analytics and the collective judgment of chemists who have to use, not just sell, this unique intermediate. Those habits reduce downstream risk, save hours in development, and result in trusted, repeatable chemistry at scale. For users with critical peptide campaigns or stereospecific routes, O-Benzyl-(D)-Serine Benzyl Ester, made by those who understand the full process, stands as a reliable tool from gram to kilogram scale. Our commitment to traceability, in-house analytics, operator know-how, and flexible manufacturing keeps each batch ready for the next challenging synthesis.