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O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride

    • Product Name O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride
    • Alias BTDSE
    • 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

    338047

    Product Name O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride
    Synonyms Methyl (2R)-2-amino-3-(tert-butoxy)propanoate hydrochloride
    Cas Number 133844-70-5
    Molecular Formula C9H20ClNO3
    Molecular Weight 225.71 g/mol
    Appearance White to off-white solid
    Purity Typically ≥98%
    Solubility Soluble in water, methanol
    Storage Conditions Store at 2-8°C, protected from light and moisture
    Optical Activity [α]D25 +21° (c=1, MeOH)
    Melting Point 115-120°C (dec.)
    Smiles CC(C)(C)OC[C@H](N)C(=O)OC.Cl
    Application Used as a chiral building block in organic synthesis
    Hazard Class Irritant (Xi)

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

    Packing & Storage
    Packing White, opaque screw-cap bottle containing 25 grams of *O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride*; labeled with product details and hazard warnings.
    Shipping O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride is shipped in secure, sealed packaging to ensure stability and prevent contamination. The product is typically transported at ambient or controlled room temperature. Appropriate labeling for hazardous chemicals is included, and Material Safety Data Sheets (MSDS) are provided to ensure safe handling during transit and upon delivery.
    Storage O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride should be stored in a cool, dry, and well-ventilated area away from direct sunlight, heat, and moisture. Keep the container tightly closed when not in use and store at 2‑8°C (refrigerator). Ensure the product is kept away from incompatible substances such as strong oxidizing agents. Handle under an inert atmosphere if sensitivity to air or moisture is suspected.
    Application of O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride

    Applications of O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride in Industrial Manufacturing

    As a dedicated producer, we focus on supplying O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride for recognized and traceable downstream industrial sectors. This specialty intermediate serves as an essential chiral building block adopted in strict synthesis environments, supporting advanced production steps in fine chemicals, small molecule pharmaceuticals, and peptide development. Below we present distinct application scenarios, each reflecting actual industry practices and regulatory standards.

    1. Chiral Pharmaceutical Intermediate Synthesis

    Pharmaceutical manufacturers utilize our material as a protected D-serine derivative during the multi-step synthesis of optically pure active pharmaceutical ingredients (APIs). The steric protection provided by the tert-butyl and methyl ester groups ensures stereochemical integrity during condensation and deprotection steps, helping meet regulatory demands for chiral purity in CNS and oncology drug candidates. Raw material input is tightly controlled to minimize racemization and support API consistency in pilot and commercial scale runs.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211: US FDA GMP for Drug Products
    • European Pharmacopoeia (Ph. Eur.) Monographs, where relevant
    • Japanese Pharmacopoeia (JP) for chiral drug synthesis

    Typical usage ratio

    • Varies from 0.8 to 1.2 molar equivalents relative to amine or acid coupling partner, adjusted by targeted yield and stoichiometry requirements

    Downstream process integration

    • Charged into high-shear reaction vessels during the selective coupling stage in multi-step batch synthesis
    • Deprotection and downstream purification follow, using preparative HPLC or crystallization

    Final product types

    • Chiral APIs for neurology, cancer therapeutics, or anti-infectives
    • Intermediates for further conversion in contract manufacturing routes
    • Regulatory submission samples for global clinical trial batches

    2. Peptide Synthesis for Biopharmaceuticals

    CDMO and biopharma plants incorporate our protected D-serine derivative in solid-phase peptide synthesis protocols, particularly for preparing D-amino acid–containing peptides. This approach improves sequence fidelity and protects stereocenters through the Fmoc/tBu strategy, facilitating batch reproducibility and rigorous impurity profiling. Such building blocks are critical in assembling synthetic peptides with high activity and metabolic stability for therapeutic and diagnostic use.

    Industry compliance standards

    • USP General Chapter <797>: Pharmaceutical Compounding–Sterile Preparations (for peptide injectables)
    • ICH Q11: Development and Manufacture of Drug Substances
    • ISO 13408: Aseptic Processing of Peptide Drug Products
    • Relevant local GMP guidelines for peptide manufacturing facilities

    Typical usage ratio

    • Generally 1.0 equivalent per target peptide position; excess of 1.05 to 1.1 may be used to drive coupling efficiency in automated synthesizers

    Downstream process integration

    • Delivered into resin-bound solid-phase reactors during elongation cycles
    • Deprotection and cleavage performed post-assembly, followed by preparative RP-HPLC

    Final product types

    • Synthetic therapeutic peptides (e.g., antagonists, hormones, antimicrobial peptides)
    • Labeled peptides for imaging
    • Research peptides for screening and validation

    3. Specialty Amino Acid Derivative Manufacturing

    Producers of high-purity specialty amino acids employ this derivate to enable selective functionalization reactions, which are subsequently deprotected for release of D-serine or complex D-amino acid analogs. The tert-butyl and methyl ester protected D-serine ensures that undesired side reactions, such as racemization or over-alkylation, are minimized during stepwise transformations, maintaining stringent quality specifications needed for regulated markets.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems for chemical manufacturing
    • Food Chemicals Codex (FCC) for food-grade D-serine, if food application pursued post-purification
    • REACH Registration, Evaluation, Authorisation, and Restriction of Chemicals (EU)

    Typical usage ratio

    • Ranges from 0.9–1.0 molar equivalents in stepwise functionalization, adjusted for process yield and desired product purity

    Downstream process integration

    • Dissolved into organic solvents for coupling or modification reactions, then processed through acid/base cleavage and solvent removal
    • Column chromatography or crystallization used for final purification

    Final product types

    • High-purity D-serine for pharmaceutical or biochemical research
    • Functionalized D-amino acid building blocks
    • Chiral auxiliaries for asymmetric synthesis development

    4. Fine Chemical Intermediate for CNS Drug Development

    Chemical developers targeting central nervous system (CNS) drug candidates frequently utilize this protected D-serine ester as a precursor in the synthesis of ligands, agonists, or antagonists for NMDA receptor studies. Robust protection allows the compound to withstand multi-step transformations including amidation, alkylation, or cyclization, which are essential in preclinical libraries for SAR (structure–activity relationship) exploration. Its application supports both lead optimization and process scaling under controlled conditions.

    Industry compliance standards

    • Good Laboratory Practice (GLP) for preclinical compound manufacturing
    • OECD Guidelines for the Testing of Chemicals (for compound libraries)
    • ISO/IEC 17025 (testing laboratories for CNS-active compounds)

    Typical usage ratio

    • Usually 1.0–1.3 molar equivalents based on the synthetic target, with excess added in scale-up batches to optimize yield

    Downstream process integration

    • Incorporated in combinatorial synthesis arrays at the protected amino acid building stage
    • Final deprotection and salt-formation precedes biological screening or analytical release

    Final product types

    • NMDA receptor ligands and probe compounds
    • Small molecule CNS drug candidates
    • Reference standards for analytical and pharmacological labs
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    Certification & Compliance
    More Introduction

    O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride: Unpacking the Value Behind a Specialized Amino Acid Building Block

    Understanding What Sets Our O-Tert-Butyl-D-Serine Methyl Ester Hydrochloride Apart

    In chemical manufacturing, producing specialty amino acid derivatives isn’t just another day at the plant. Each compound we release draws on the experience of teams that have faced firsthand the challenges and intricacies of scaling up from bench to bulk. O-Tert-Butyl-D-serine methyl ester hydrochloride (model: OBDSM-HCl) reflects this technical depth.

    O-Tert-Butyl-D-serine methyl ester hydrochloride lands in a family of protected serine derivatives, but right away, you notice the subtle differences. Peptide chemists and small molecule researchers have discovered that the tert-butyl protection makes a real impact during synthetic sequences. In hands-on terms, that lateral protection can make or break yield when tackling tough couplings, and those of us running production lines see it every day. The tert-butyl group stays secure under conditions where less robust protecting groups such as benzyl or acetyl would fall apart. That reliability matters in both pilot work and multi-kilo custom projects.

    O-Tert-butyl-D-serine methyl ester hydrochloride steps into applications where an easy deprotection at the right stage is necessary for purity and yield. That’s a sticking point we see labs risk every time they select the wrong protected amino acid. Unprotected D-serine methyl ester could hydrolyze or react prematurely, and other groups sometimes don’t handle TFA or moisture the way tert-butyl does. By using tert-butyl, chemists get extra margin of safety, avoiding side reactions that lower the quality of the target molecule. Drawing on our batch records and project histories, we have seen production runs saved by that kind of stability.

    The Features That Support Complex Synthesis

    The backbone of this molecule is D-serine, not the L-form you see in proteinogenic contexts. Choosing the D-isomer can be costly in terms of starting materials and enantiomeric control, but sometimes selectivity, biological activity, or patent coverage makes it worth every gram. For our OBDSM-HCl, we use rigorous chiral resolution and enantiopurity testing, because small deviations cascade into lost value down the line. For pharmaceutical development, even a trace of the L-isomer can derail months of analysis.

    The methyl ester on the side chain seems like a simple swap, but try running a multi-step process with hydrolyzable esters and you quickly see the headaches of unwanted saponification. Our process engineers pay attention to every solvent, pH adjustment, and trace of water to minimize these risks. Some generic versions of O-tert-butyl protected serine esters overlook these subtleties, and researchers face crystallization issues or lower purity. Our process steps make a difference in minimizing those impurities that stall downstream scale-up.

    The final hydrochloride salt gives OBDSM-HCl the solubility and handling profile that ask for less fuss in purification and weighing. It doesn’t form sticky clumps like the free base, and it shows predictable behavior whether you’re making 5 grams or 20 kilograms. From our position on the manufacturing floor, we see the real difference a good hydrochloride form brings when handling tonnage or automating a process step.

    Industry Applications and Our Experience in Supplying OBDSM-HCl

    Over the last decade, we have supplied O-tert-butyl-D-serine methyl ester hydrochloride to process chemists, medicinal chemists, and peptide houses worldwide. Its main value shows up in custom peptide synthesis, especially for sequences where D-amino acids play a functional role—be it in research targets, peptidomimetics, or in advanced pharmaceutical intermediates. D-serine derivatives have emerged as building blocks for NMDA receptor modulators, bioactive peptides, and antimicrobial agents, and the tert-butyl protection lets these developers streamline the stages leading up to final deprotection.

    Pharmaceutical research teams in advanced synthetic projects often run up against side reactions at late stages. The solid performance of tert-butyl protection keeps unwanted hydrolysis in check. We have worked on collaborations where supply reliability mattered more than ever during scale-up—from milligram-level optimization to preclinical batch production. The teams that ordered OBDSM-HCl saw lower batch failure, less time spent troubleshooting, and faster regulatory documentation after they switched from lower-grade counterparts.

    Comparing to Other Serine Derivatives and Amino Acid Building Blocks

    Some might ask what makes OBDSM-HCl more than just another protected amino acid. The difference shows up both in chemistry and in operational detail. Compare it with Fmoc- or Boc-protected serines. The tert-butyl group on OBDSM-HCl stays put under moderately strong acid, especially in the presence of nucleophiles. Boc groups can drop off in extended or heated reaction times, and Fmoc deprotection can get messy if the timeline isn’t right. We have answered countless technical support calls from chemists frustrated by sluggish or incomplete deprotection steps with other serine esters.

    Looking at methyl versus ethyl esters, you get subtle but real differences in handling and eventual removal. Methyl esters hydrolyze more predictably and cleanly; this streamlines downstream purification, saving hours in chromatography and crystallization steps. During multi-ton plant projects, these hours add up fast—raw material price becomes a small line item compared to lost processing time. Our product offers this reliable handling, reducing both chemical risk and process downtime.

    Manufacturing Challenges and the Steps Taken to Ensure Consistency

    Manufacturing O-tert-butyl-D-serine methyl ester hydrochloride at commercial scale is far from routine. We battle challenges involving steric protection, moisture control, purification, and product isolation. Early on, the largest hurdle came with clean isolation of the hydrochloride salt, which exhibits deliquescence in humid environments. Packaging the product for global shipment led to site upgrades, including humidity-controlled warehouses and nitrogen-purged storage. We backed this with quartile-based stability studies, identifying critical limits for both moisture and temperature so that every drum ships with quality documentation the customer can verify.

    Beyond physical challenges, the need for chiral purity stretches out our process timelines. Achieving greater than 99% enantiopurity called for close work with HPLC method developers. Once shipped to customer labs, the last thing needed are concerns about epimerization—so we check every lot by optical rotation and validated chromatographic methods. This commitment to purity may slow some batches, but we have learned the cost of shortcuts from studying failed runs by other suppliers.

    Quality Support Gained from Real-world Feedback

    Direct conversations with R&D chemists taught us valuable lessons about what matters in daily lab and plant operation. Requests often came in for small-scale, high-purity batches where the focus fell on avoiding trace metal contamination or residual solvents. To deliver on these needs, we retrofitted crystallization taints, set up dedicated lines for custom purification, and put a process in place for post-production QA release through gas chromatography and ICP-MS analysis.

    One benefit of being the manufacturer, not a broker, is having deep oversight into every stage of the process. We match our certificate of analysis with process records that customers can audit. This direct traceability wins trust with pharma and academic partners who need to defend their own batch records.

    Cost control is another demand coming from both large and boutique buyers. By controlling raw material stocks, solvent handling, and shipping, we maintain predictable pricing, regardless of the vagaries of the spot market. This predictability allows our partners to plan budgets and forecast based on actual commercial sourcing rather than hope or uncertainty.

    Handling and Storage—From the Operator’s Perspective

    On the production floor, OBDSM-HCl offers advantages that aren’t obvious from a catalogue page. Its free-flowing crystalline powder handles smoothly through enclosed transfer lines, with minimal dusting—a factor that operators appreciate during long-night campaigns. A few years back, we rolled out better drum liners and moisture-barrier packaging after seeing too many clumped bags from vendors with less attention to humidity. Since then, complaints of “rock-hard” blocks in transit have dropped sharply.

    The shelf life under controlled conditions extends several months, giving users enough flexibility in custom and scale-up projects. Some other derivatives decay or pick up color over time due to marginal impurity levels. Our anti-static, UV-blocking packaging emerged not from theory, but from watching early shipments degrade and learning from lost inventory.

    Environmental and Regulatory Considerations

    Operating in today’s regulatory environment, we know simply meeting a monograph isn’t enough. End-users expect a transparent breakdown of all process controls, a statement on metal residues, and a clear explanation of how we handle waste streams. Our plant design implements solvent recovery, two-stage filtration for aqueous waste, and an automated monitoring system for effluents. The O-tert-butyl group, while easy to remove chemically, needs special attention in waste management due to its resilience. By investing in in-house incineration for tert-butyl waste fractions, we cut down on outsourced disposal fees and reduce regulatory exposure for ourselves and our partners.

    Raw material tracking extends through our supply chain, so regulatory agencies or customers never face surprises about obscure intermediate sources. Documentation rides with each shipment, cutting down on back-and-forth and accelerating lab clearances. Based on requests from the biopharmaceutical sector, we have included ICH Q7 and US FDA audit readiness documentation with each large-scale delivery.

    Customer Support Rooted in Manufacturing Experience

    As a company focused on direct production, our support goes beyond off-the-shelf documentation. R&D labs face unexpected scale-up hurdles—loss of optical purity, handling issues at lower temperatures, or trouble with downstream ester removal. Over the years, we have assisted customers by sending technical staff to their sites when needed, and by troubleshooting alongside them during critical troubleshooting moments—even after hours.

    Our technical team stands ready to answer application-specific questions, drawing not only on published data but on firsthand plant experience. Chemical manufacturing always throws curveballs, but it helps to have access to staff who know the technology, not just the paperwork.

    Research Trends and the Role of Protected D-Serine Esters

    Research in the last five years has highlighted how D-amino acids, especially protected analogues, impact biological function and confer stability to therapeutic peptides. A surge in research papers and patents shows a growing interest in D-serine containing peptides, peptidomimetics, and modified enzymes, as well as new synthetic pathways leveraging tert-butyl-protected intermediates. Peptide structure-activity relationship studies point to improved selectivity and metabolic stability in sequences using tert-butyl-D-serine methyl ester derivatives.

    The adoption of OBDSM-HCl by life sciences firms stems from published studies and case reports, but sustained satisfaction comes from batches that deliver on chromatographic purity and elemental analysis, batch after batch. Having supplied both large multinational companies and specialized academic teams, we see the confidence our product brings to research leaders.

    Continuous Improvement Through Feedback

    Our commitment to O-tert-butyl-D-serine methyl ester hydrochloride doesn’t end at the plant gate. Each quarter, we review process feedback and field logs for common customer complaints and returns. This cycle of improvement led to adjustments in crystallization cycles, packaging type, and shipping frequency. That iterative approach means less risk of batch failure for new customers and more troubleshooting support for repeat buyers.

    Our direct engagement with researchers led to the design of small, research-grade packs with maximum shelf-life as well as bulk options for commercial scale. Academic partners benefit from flexibility in lot size, while commercial partners can lock in price and supply for multi-year development timelines.

    Why Manufacturers Trust Their Supply to a Direct Producer

    Chemists who select O-tert-butyl-D-serine methyl ester hydrochloride from a direct manufacturer value more than just a line item or a purity specification. We understand the difficulty of sourcing minor building blocks with complex protection, and we back every shipment with our full technical team and laboratory data. By working directly with manufacturing, research teams avoid the pitfalls of variable quality, opaque sourcing, or inconsistent delivery schedules that sometimes shadow third-party distributors.

    We’ve seen projects rescued by quick access to new lots, and new methods developed after confidential technical exchanges between our technical group and customer labs. Years standing behind OBDSM-HCl has given us a unique vantage—tracking industry trends, regulatory shifts, and new research demands as they emerge.

    Conclusion: Experience Drives Product Value

    O-tert-butyl-D-serine methyl ester hydrochloride stands as more than an off-the-shelf protected amino acid. Drawing from the experience of years managing production, confronting technical challenges, and listening to the practical needs of chemists, we push to deliver product that becomes a reliable input for researchers and process developers. Through refining methods, improving packaging, and supporting each new application, manufacturing excellence is the backbone behind this critical reagent. Each shipment carries the history and attention to detail that comes only from those who have been responsible for every step of its creation, making a difference from R&D benches up to full-scale production suites.