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N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol

    • Product Name N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol
    • Alias (S)-Boc-Amino-Benzyloxy-Propanol
    • 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

    780713

    Product Name N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol
    Molecular Formula C15H23NO4
    Molecular Weight 281.35 g/mol
    Cas Number 110036-65-6
    Appearance White to off-white solid
    Optical Purity S enantiomer
    Melting Point 72-75°C
    Solubility Soluble in organic solvents such as dichloromethane and ethanol
    Storage Conditions Store at 2-8°C in tightly closed container
    Protecting Group Boc (tert-butoxycarbonyl) on amine
    Functional Groups Amino, benzyloxy, Boc-protected amine, alcohol
    Chirality Chiral; typically supplied as (S)-enantiomer

    As an accredited N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol, 5g, supplied in a sealed amber glass bottle with tamper-evident cap, labeled for research use.
    Shipping N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol is shipped in tightly sealed containers under cool, dry conditions to prevent degradation or contamination. Packaging meets standard safety regulations for chemical transport. Accompanied by a Safety Data Sheet (SDS), it is handled as a non-hazardous, stable compound unless otherwise specified by regulatory guidelines.
    Storage Store N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol in a tightly sealed container under an inert atmosphere, such as nitrogen or argon, to prevent moisture and air exposure. Keep it in a cool, dry place, preferably at 2–8 °C, away from heat, light, and incompatible materials like strong acids and oxidizers. Use appropriate personal protective equipment when handling.
    Application of N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol

    Applications of N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol in Industrial Manufacturing

    N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol serves as a core intermediate in pharmaceutical, chemical synthesis, chiral technology, and biotechnology sectors. As an experienced manufacturer, we support industrial users in integrating this key material into downstream production with certified quality, traceability, and technical documentation. Below are the primary application fields with related technical and compliance insights.

    1. Peptide Active Pharmaceutical Ingredient (API) Synthesis

    Manufacturers employ this compound as a protected amino alcohol building block for stepwise peptide assembly, where the N-Boc and benzyloxy groups provide orthogonal protecting strategies during couplings. Process chemists rely on it for preserving stereochemical integrity throughout multi-step solid-phase or solution-phase peptide synthesis, including custom and GMP-grade oligopeptides. Consistency, purity, and low-residual solvent levels remain essential for regulatory approval and batch reproducibility.

    Industry compliance standards

    • ICH Q7/Q11 for API manufacturing
    • USP/NF and Ph. Eur. monograph requirements for peptide drug substances
    • FDA cGMP (21 CFR Part 210/211)
    • EDQM Certificate of Suitability (CEP) where applicable

    Typical usage ratio

    • 0.9–1.2 molar equivalents per protected residue in coupling cycles; ratio adjusted for resin loading, efficiency, and scale

    Downstream process integration

    • Added during elongation stages to introduce BOC- and benzyloxy-protected residues on the solid support or in solution
    • Undergoes selective deprotection prior to coupling or cyclization steps

    Final product types

    • Therapeutic peptides (hormonal, metabolic, oncology, and rare disease APIs)
    • Custom oligopeptide libraries for drug discovery
    • Intermediates for protected peptide fragments
    • Conjugated biomolecule drugs

    2. Chiral Auxiliary in Small Molecule Synthesis

    The molecule is applied as an enantiomerically pure auxiliary for asymmetric synthesis of alcohols, amines, and β-amino acid derivatives. Its structural features enable chemists to control stereoselectivity in key transformations, including addition, reduction, and cyclization reactions. Downstream users rely on high chemical purity and low enantiomeric excess variability, as mistakes at this step impact overall drug quality and regulatory compliance.

    Industry compliance standards

    • ICH Q3A/B for impurity and enantiopurity control
    • FDA guidelines on chiral APIs and intermediates
    • Relevant Ph. Eur. monographs referencing chiral purity
    • ISO 9001:2015 quality system implementation

    Typical usage ratio

    • 0.95–1.05 molar ratio relative to the substrate; process optimization may change loading depending on target architecture

    Downstream process integration

    • Introduced in the initial or mid-stage steps of chiral catalyst or auxiliary incorporation
    • Removed post-transformation without racemization and recycled where possible

    Final product types

    • Chiral pharmaceutical intermediates
    • Asymmetric synthesis products (amino alcohols, β-lactams)
    • Advanced key intermediates for antihypertensive or anti-infective drugs
    • Fine chiral specialty chemicals

    3. Oligonucleotide Conjugation Chemistry

    Producers of antisense oligonucleotides and nucleic acid-based therapeutics adopt this intermediate as a chiral linker or branching unit during solid-phase manufacturing. The compound’s protecting groups confer stability through harsh synthetic cycles, maintaining sensitive functionalities until final deprotection and conjugation. Specialist oligonucleotide houses require full traceability of raw material production and rigorous documentation to meet regulatory filings.

    Industry compliance standards

    • FDA cGMP for oligonucleotide drug substances (DS/DP)
    • EMA Guidelines on quality for oligonucleotide-based drugs
    • Vendor audit and traceability frameworks
    • Regulatory filings referencing DMF/ASMF where applicable

    Typical usage ratio

    • 0.8–1.0 molar equivalent per conjugation site on nucleotide strands; ratio set according to strand length and conjugation density

    Downstream process integration

    • Reacted onsite during advanced coupling or branching steps of nucleotide solid-phase assembly
    • Undergoes orthogonal deprotections followed by purification and desalting

    Final product types

    • Antisense oligonucleotide drug substances
    • RNA/DNA-based therapeutics with chiral linkers
    • Nucleic acid-drug conjugates
    • Branched or multi-functional oligonucleotide research reagents

    4. Specialty Protecting Group for Advanced Organic Synthesis

    N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol is routinely incorporated as a highly selective protecting group in multi-step synthesis of complex, high-value molecules. Its robust N-Boc and O-benzyl protections allow sequential orthogonal manipulation, especially in the manufacture of advanced pharmaceutical intermediates and custom ligands for chemical biology. Companies prioritize batch consistency, minimal by-product formation, and fully validated synthesis records for audit purposes in these applications.

    Industry compliance standards

    • GMP or ISO 9001:2015–certified production
    • Good Documentation Practice (GDP) for synthesis batch records
    • Change control management for process validation
    • Chemical Hazard Communication (OSHA/HCS, EU CLP)

    Typical usage ratio

    • 1.0–1.5 equiv per protected functional group; increased ratios for high-yielding or large-scale processes

    Downstream process integration

    • Employed at intermediate or penultimate stages to safeguard functional groups from unwanted side reactions
    • Removed selectively through hydrogenation or acidolysis after core transformations

    Final product types

    • API advanced intermediates
    • Custom fine chemicals for research and development
    • Synthetic reference standards
    • Ligand scaffolds used in catalysis or molecular recognition
    Free Quote

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    Certification & Compliance
    More Introduction

    N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol: Delivering Real Value in Chiral Building Blocks

    Product Introduction

    We produce N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol at our own facility, with a focus on rigorous quality and reliable traceability all the way from the incoming raw material drums to the finished vials. Through years of batch manufacturing and direct feedback from chemists who use this intermediate every day, we know its strengths and critical features. The model we supply most often carries a CAS number of 138720-95-1 and offers a chemical purity that consistently exceeds 98.5% by HPLC, without the lingering off-odor or coloration found in material handled through long supply chains. Each batch gets checked not only by in-process controls but also through full characterization—NMR, HPLC, and chiral GC—so you can trust what arrives.

    Why This Chiral Alcohol Matters

    N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol fills a narrow but important niche. The molecule starts with the protected amine, which means you skip tedious protection steps during early-phase route scouting. Paired with its benzyloxy group, it offers a protected, easy-to-handle version of a chiral 1,3-diol fragment, so process chemists have fewer worries about racemization or oxidative loss under standard lab conditions. In our own operation, we found less stable intermediates forcing too much cold-chain transport or making for sticky residues with unreliable purity. Customers building β-amino alcohol-based drugs or peptidomimetic sequences have told us this intermediate saves at least two steps per campaign, especially during the scale-up run. The time and cost advantages become clear when you do the math on labor, cleanup, and recovery for chromatography purifications.

    Direct Production Brings Real Benefits

    As the actual manufacturer, we control every aspect. Starting from amino acids of defined optical purity, our bottleneck never involves spent raw materials or uncertain stock. We watch all side streams, right down to each solvent swap. To keep the (S)-enantiomer pure, our technicians tune the Boc protection timing to minimize byproducts, which usually show up as ghost peaks in third-party material. Often, material resold by traders lands with variable particle size or subtle yellow tint from trace benzylic oxidation; our cleanroom logistics and short supply pipeline stop those issues at the source.

    Batch reproducibility has been a lesson in solving real-world chemistry challenges. In the early years, solvent choice alone swung the content of the byproduct over 0.5%. After continuous improvements and hundreds of feedback cycles, our standard production protocol drops this to under 0.1%, batch-to-batch. That puts us ahead of most resellers we’ve compared, whose material often comes from at least two middlemen or contract filler plants before hitting the market.

    Performance Differences: Not All Material Is Equal

    In-house analytical chemists track what happens to our product under the usual conditions: freezing, heating, and several pH levels. Our own trials include using N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol in both single-pot and two-step reactions, showing it holds up under basic and mildly acidic workups. When material is made indirectly or left on dusty warehouse shelves for weeks, you start encountering partial hydrolysis or subtle racemization—not easy to spot until you scale up. We ship quickly after manufacture for exactly this reason, and store nothing in long-term tankage.

    Many generic samples floating around global markets come with visible heterogeneity. Sometimes the crystals look like two populations mixed together, or yield strange melting behavior—these often coat stirrers and glassware, slowing down the next step. Our process delivers single, free-flowing crystals with a narrow melting range, so weighing goes fast and handling stays clean. Moisture pickup is under control, thanks to closed packaging directly after filtration and drying. For labs worried about cross-contamination or inconsistent yield, these are not small issues.

    Real-World Usage in Synthesis Labs and Plants

    Labs using this chiral auxiliary usually focus on complex targets: β-amino alcohols, peptidomimetic scaffolds, or other molecules where chirality can't be left to chance. For at least a decade, the dominant demand comes from drug discovery teams—the Boc and benzyloxy groups both hold up well during acid-sensitive or basic cascade sequences. One pharma client involved in kinase inhibitor routes highlighted how easy deprotection was with standard TFA protocols, without extra scavengers or side product headaches.

    We keep in ongoing contact with process scale-up chemists, hearing first-hand what happens during pilot-plant campaigns. Over 60% of complaints about outsourced or reseller product relate to variable reactivity, which means more time spent troubleshooting, extra purification, or simply lost product. Our standard responsiveness can be traced directly to our own experience working on site, where pressure to hit tight timelines matches safety and regulatory headaches. That experience drives our protocol choices: always offering fresh analytics, lot-to-lot sample vials, and overnight answers whenever something looks off.

    Downstream Flexibility: One Intermediate, Many Approaches

    Chemists value this material because the protected chiral center allows for diverse transformations. Some groups hydrogenate and remove the benzyloxy group in a single pot, streamlining late-stage routes. Others keep the Boc-protection through several coupling steps, only removing it at the end. In several recent custom campaigns, we ran pilot-scale synthesis for exploratory routes and found the product’s stability in standard glass reactors—without noticeable loss in yield—even after several days at cold or ambient temperatures.

    Developers in the peptide sector sometimes call to confirm batch scalability, since the impact of trace side-products rises with each multigram scale-up. At 100g, a 0.2% impurity translates to a major chromatography headache; with our product, these impurities remain visible only by detailed 13C NMR, well below user limits. We built our production with such realities in mind: by minimizing water tracks and cutting back on unnecessary solvents, handling and purity stay predictable.

    Regulatory and Traceability Experience

    Certifications matter. For regulated and semi-regulated pharma groups, a transparent production chain eliminates most of the compliance headaches. We back each lot of N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol with a sealed analytical pack, signed off by QA, including raw analytical printouts—not just a one-line summary. Auditors and project managers can see the original data, right down to LCMS traces. Since our facility includes GMP-aligned records, we can revisit production logs or quickly release supplementary certificates by request. When audits come, this level of paper trail shortens site visits and smooths out approval cycles.

    Lessons Learned Producing This Building Block

    Scaling up N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol has shown how much small choices impact success. We learned early that trying to shortcut reagent quality or batch control always caught up with us. For example, the Boc-anhydride source made a measurable difference in product color and purity—one lot of raw material led to significantly more yellowing and off-residue. We shifted suppliers and never looked back. Water control has been just as critical, as trace amounts changed chiral purity by fractions of a percent that only became clear once final NMR, not just test runs, came back.

    Waste minimization became part of our workflow, not just an afterthought. By recycling non-chlorinated solvents and dialing batch charging by real yield, reactor downtime dropped. These changes created both environmental and cost benefits, so delivery lead times shortened and every penny saved went straight to customers rather than inventory costs.

    Comparisons to Related Building Blocks

    Plenty of other amino alcohols or similar chiral auxiliaries come in at a lower price or with a longer shelf life, but in our hands, none balance the dual protection and chiral integrity as cleanly. For example, basic 2-amino-1-propanol comes cheaper and less protected, but needs extra workup and protection-deprotection rounds, raising time and waste. Products missing the benzyloxy group lose reliability in later O-deprotection steps and often deliver lower final yields in downstream APIs.

    Our N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol holds a clear edge over similar mono-protected systems, especially in terms of handling. Some alternative chiral alcohols come preloaded with protected amines but lack the stability for scale-up or open-air handling. Those alternatives produce more variable byproducts and sometimes require stepwise purification between every transformation. Our process, refined by repeated troubleshooting, gives a building block stable on the bench but reactive enough for single-step couplings. The practical results show up in higher yields, simpler workup, and faster project deliverables reported by process chemists.

    From Lab to Kilo-Scale: Practical Impacts

    The leap from flask-scale to kilogram batches requires process controls that look simple but take experience to dial in. Early on, we struggled to maintain tight density and melting point specifications until investing in continuous sampling and in-line drying. By training operators to recognize subtle color or texture shifts, we trimmed rejection rates. Our kilo-batch output now shows less than 0.05% variance in chemical assays across lots, reducing the need for backblending or splitting batches. Customer campaigns move faster this way because there’s less need for re-validation between shipments.

    We also learned to monitor energy and time tightly. Inefficient stirring, heating, or cooling not only stretched batch times but also introduced more variability. By applying granular tracking, each batch now fits a predictable timeline. Customers can plan multistep syntheses with higher reliability, easing pressure on both research and manufacturing teams.

    End-User Feedback Shapes Continuous Improvement

    Chemists’ feedback—both positive and critical—forms the backbone of our improvements. Reports of sticky residues led us to revise drying protocols and enhance packaging seals. Accounts of odd side-product peaks on specialized HPLC columns prompted us to buy new reference standards and expand our in-house analytical capabilities. We encourage users to reach out with any anomalies, as collaborative transparency drives real progress. It’s this kind of back-and-forth, rather than just box-ticking safety or compliance, which leads us to real-world solutions and long-term partnerships.

    Reliable Supply, Real Confidence

    Managing production end-to-end gives us more control over quality and supply chain disruptions. Weather events, regulatory shifts, and transport delays haven’t stopped us from shipping on schedule for over five years running. By holding critical raw materials in a secure warehouse, we keep timelines tight. If users want to reserve batches ahead or need split shipments, we can match to their schedule. This isn’t just a selling point—it’s daily operational reality brought by direct manufacturing experience.

    Sustainability and Responsible Practices

    Environmental responsibility and sustainable sourcing figure into our operational choices. Whenever possible, we avoid halogenated solvents, trim energy and water use, and repurpose byproduct streams. Our plant design features solvent capture to cut emissions and reduce workplace hazards. These adjustments help us offer a cleaner product that fits with downstream regulatory filings and environmental stewardship standards. Companies building long-term projects see this as more than a checkbox—it’s a safeguard for both process budgets and work safety.

    Technical Support and Ongoing Partnership

    We don’t lock our product behind an order form—chemists, managers, and scale-up teams contact us before synthesis planning begins. If there’s doubt about compatibility with novel reagents or specific downstream transformations, our technical team draws on both hands-on experience and extensive batch data. We share best practices for storage, handling, and safe deprotection to keep each project predictable. When unique purities or physical forms are called for, we can tune our process—sometimes running special drying or sieving cycles that provide exactly what the project targets demand.

    In cases of unexpected outcomes—like unusual chromatographic patterns or reaction delays—users often send details, letting us troubleshoot with real chemical insight rather than generic instructions. Our persistent involvement supports both product improvement and customer success, beyond the ordinary transactional approach.

    Conclusion: Value of Direct Manufacturing

    Making N-Boc-(S)-2-Amino-3-Benzyloxy-1-Propanol ourselves, batch after batch, means there are no shortcuts or mysteries. Our experience as the source, not a reseller or repacker, delivers real advantages: a stable supply, consistent quality, and responsive support for every step of the research or manufacturing process. Chemists can trust that what they receive matches not only the highest analytical standards but also the real-world demands of daily bench and plant operations.