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Boc-D-Prolinol

    • Product Name Boc-D-Prolinol
    • Alias (S)-Boc-pipecolinol
    • Einecs 696-617-6
    • 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

    741825

    Product Name Boc-D-Prolinol
    Synonyms tert-Butoxycarbonyl-D-prolinol
    Cas Number 100911-12-6
    Molecular Formula C10H19NO3
    Molecular Weight 201.26
    Appearance White to off-white solid
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Solubility Soluble in organic solvents such as methanol, ethanol, and dichloromethane

    As an accredited Boc-D-Prolinol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Boc-D-Prolinol is supplied in a sealed amber glass bottle, containing 25 grams, labeled with product name, purity, and safety warnings.
    Shipping Boc-D-Prolinol is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be handled by trained personnel wearing appropriate personal protective equipment. Standard shipping is typically via ground or air freight in compliance with chemical transport regulations to ensure safety and product integrity during transit.
    Storage Boc-D-Prolinol should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of heat and moisture. Protect it from direct sunlight and incompatible substances such as strong acids or oxidizers. Ideally, store at 2–8°C (refrigerator temperature) and ensure proper labeling to avoid confusion. Avoid prolonged exposure to air and humidity.
    Application of Boc-D-Prolinol

    Applications of Boc-D-Prolinol in Industrial Manufacturing

    Boc-D-Prolinol serves as a precision chiral intermediate in multiple high-value industrial sectors. As a direct manufacturer with multi-ton capacity, we address the stringent demands of pharmaceutical, agrochemical, and fine chemical synthesis. Below, explore authentic downstream applications and technical parameters across key industries.

    1. APIs: Peptidomimetic Pharmaceutical Synthesis

    Pharmaceutical producers incorporate Boc-D-Prolinol as an intermediate for chiral peptidomimetics, including protease inhibitors, DPP-4 inhibitors, and neuroactive compounds. Its N-protected structure and secondary alcohol facilitate stereoselective coupling, enhancing molecular complexity and enantiomeric purity. Strict process control minimizes racemization, ensuring traceability through GMP-compliant batch records. Applications center on small molecule drugs where chiral amine building blocks are essential for regulatory filing and clinical development.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) guidelines for chiral intermediates
    • US FDA 21 CFR Part 211 for API synthesis
    • Consistency with DMF submissions and traceability documentation

    Typical usage ratio

    • 0.85–1.10 molar equivalents per chiral center, adjusted according to specific peptide or heterocycle synthesis routes
    • Optimized by in-process HPLC monitoring for overages below 5% for regulated waste control

    Downstream process integration

    • Introduced post-condensation as a chiral secondary alcohol segment with Boc-protection intact
    • Boc group removed under acidic conditions before final amide or ester bond formation
    • Employed in reductive amination, cyclization, or amidation workflows under controlled temperature and inert atmospheres

    Final product types

    • DPP-4 inhibitors for metabolic disorder therapeutics
    • Peptide-mimetic drugs targeting CNS indications
    • Small molecule antivirals leveraging chiral proline analogues
    • Generic and branded APIs using protected D-prolinol units

    2. Agrochemical Intermediate for Stereoselective Pesticides

    Boc-D-Prolinol is a key intermediate in the manufacture of chiral agrochemical actives, particularly heterocyclic crop protection agents and herbicide analogues. Leading agrochemical firms value its robust performance in scale-up synthesis due to reliable protection and deprotection. Manufacturers use this intermediate to construct asymmetric centers, improving biological activity and regulatory approval success. Detailed batch documentation supports regional agrochemical compliance.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO pesticide specifications for raw material traceability
    • REACH regulations for preservatives and intermediates
    • ISO 9001:2015 for QMS in chemical production

    Typical usage ratio

    • 1.0–1.2 molar equivalents per asymmetric center, modulated based on substrate reactivity and scalability targets
    • Analytical verification at each stage controls excess and minimizes downstream impurities

    Downstream process integration

    • Applied after initial heterocycle formation to establish chiral configuration through amide/ester linkage
    • Deprotection performed directly before introduction of active pesticide functional groups
    • Final coupling or cyclization executed in solvent systems compatible with agrochemical standardization

    Final product types

    • Enantiomerically enriched herbicides for selective weed control
    • Fungicide intermediates leveraging chiral backbone functionality
    • Custom crop protectants registered in EU/US markets
    • Biopesticide candidates under development with documented chiral purity

    3. Chiral Ligand Synthesis for Asymmetric Catalysis

    Fine chemical and catalyst manufacturers utilize Boc-D-Prolinol as a precursor for chiral ligands, especially proline-derived phosphines and imines. These ligands drive advanced asymmetric hydrogenation and organocatalysis in pharmaceutical and specialty chemical lines. The protected amine improves handleability and reproducibility in ligand construction, supporting strict internal QC and external validation for catalyst suppliers and chemical firms.

    Industry compliance standards

    • ISO 9001:2015 for development and supply chain traceability
    • REACH Annex IX for intermediates in fine chemical manufacturing
    • OECD GLP for catalyst validation data
    • Company SOPs for batch conformity and lot release

    Typical usage ratio

    • 0.95–1.00 molar equivalents per ligand backbone, with slight excess for moisture-sensitive reactions
    • Process trials may adjust ratios ±5% based on scale and ligand type

    Downstream process integration

    • Engaged at ligand core assembly stage, often as an N-protecting group for amine stabilization
    • Subjected to controlled deprotection prior to complexation with transition metals or organic frameworks
    • QC uses NMR and chiral HPLC to confirm structural identity pre- and post-complexation

    Final product types

    • Chiral phosphine ligands for asymmetric hydrogenation
    • Organocatalysts for fine chemical synthesis
    • Metal-ligand complexes targeted at API and agrochemical intermediates
    • Commercial chiral additives for enantioselective transformations

    4. Protected Alcohol Source for Specialty Polymer Synthesis

    Specialty chemical producers leverage Boc-D-Prolinol as an initiator or comonomer in the synthesis of chiral specialty polymers. Its bifunctionality aids in controlling polymer chain architecture, cyclization, and end-group modification, which are critical to high-performance materials in biomedical and analytical device markets. The Boc moiety serves as a temporary blocking group, vital in stepwise polymer development and downstream analytical validation.

    Industry compliance standards

    • ISO 13485 compliance for medical device component raw materials
    • USP Class VI specifications for polymer component biocompatibility
    • ISO 9001:2015 for quality assurance in polymer synthesis
    • Internal validation protocols for chiral additive integration

    Typical usage ratio

    • 2–10 wt% relative to total monomer mass, fine-tuned for desired chiral or functional end-group density
    • Monomer ratios optimized through Gel Permeation Chromatography (GPC) to balance molecular weight and stereoregularity

    Downstream process integration

    • Used as an initiator or co-monomer in step-growth or ring-opening polymerizations
    • Boc group removed under controlled acidic or thermal conditions prior to functionalization or medical validation testing
    • Chain-terminating or post-polymerization modifications introduced for tailored device compatibility

    Final product types

    • Chiral stationary phase polymers for analytical separations
    • Biomedical hydrogels and scaffolds with controlled architecture
    • Device-grade nano- and microstructured materials for diagnostics
    • Specialty polymeric excipients for advanced formulation applications
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    Certification & Compliance
    More Introduction

    Boc-D-Prolinol: Reliable Building Block Backed by Consistent Chemistry

    Understanding the Core Value of Boc-D-Prolinol in Synthesis

    Boc-D-Prolinol has earned its place in the toolbox of many synthetic chemists because its properties help bridge the gap between creative route planning and scalable execution. As a manufacturer, we have focused on strengthening the reliability of each batch, centering our approach on what we have learned from years spent at the reactor and purification line. We know that there’s no room for deviation in a critical intermediate, and Boc-D-Prolinol’s role in asymmetric synthesis reflects that. Our experience supplying gram to multi-kilo lots for pharmaceutical innovators, contract manufacturing organizations, and research labs has made it plain: no two processes are quite the same, and nuanced control over stereochemistry is a constant concern. Boc-D-Prolinol, protected by the tert-butyloxycarbonyl (Boc) group at the nitrogen, brings a well-defined chirality and functional freedom that lets process chemists conserve both time and resources.

    Every lot starts with raw material traceability, and each reactor charge follows internal protocols that grew out of years merging small-batch and plant-scale synthesis. Our production lines balance control and throughput—with D-proline as our single enantiomeric source, we monitor stereopurity using chiral HPLC and further check for low-level impurities at every step, knowing that downstream steps can amplify even minor contamination. Some may look only at purity on the certificate of analysis, but our operators see firsthand the essential value in keeping diastereomeric ratios steady and meeting the tight limits on heavy metals and residual solvents. Experienced chemists, including those who spend their days running solid-phase peptide syntheses or pushing nitrogen-protected amino alcohols into custom scaffolds, often share feedback about challenges they’ve encountered with unreliable supply chains. That feedback steers decisions about what improvements to keep in production, helping us stay vigilant with change control and analytical method validation.

    Differentiating Boc-D-Prolinol Beyond Spec Sheets

    It’s tempting to compare Boc-D-Prolinol by its CAS number or adjust the focus to basic attributes like assay or moisture content. From the eyes of someone who makes the stuff, too much emphasis on catalog labels misses the lived differences that matter on a kilo scale. Our typical supply comes as a white to off-white crystalline solid, stable under refrigeration and easy to store in double-lined PE bags and fiber drums. The free amine gets thoroughly protected by our own Boc installation process—a method we’ve adapted to avoid n-alkylation side reactions that plagued early syntheses decades ago. Environmental and safety standards drive solvent recovery and minimize emissions, but the finer details lie in the batch records. Our team tracks reaction exotherms, tweaks reaction times for full conversion, and never releases a batch without triple-verification of both mass balance and spectral characterization.

    Not all Boc-D-Prolinol you see on the market comes with the same confidence. Some vendors buy from fluctuating third-party sources; they may blend lots to keep up with orders. For anyone ironing out a new synthetic route, that inconsistency can spell process variance, missed yield targets, and failed purifications. We keep our production “closed loop,” drawing from our own proline stock, keeping control over the stereochemistry, and only bringing in external testing for final method robustness. While paper specs like [α]D match from one supplier to the next, scrutiny over hydrolyzable impurities, storage stability, and absence of unreacted amine can yield major differences at the bench. Customers with scale-up experience often notice that subtle variances—such as presence of unreacted starting material or byproducts like Boc anhydride—affect product solubility, lead to fouling during crystallizations, or confuse downstream deprotection.

    Supporting Real-World Application: From Lab Bench to Plant Scale

    As the scope of D-prolinol derivatives expands, we find that Boc-D-Prolinol slots into more routes every year—especially peptidomimetic drug discovery, chiral auxiliaries, and engineered catalyst production. Our partners in both academic and commercial sectors repeatedly ask for assurance on more than basic “purity.” They want to know about batch reproducibility, how many hands the product changes before it enters their glassware, and whether the documentation stands up to regulatory audit. These requests shape our process: every certificate we issue comes from direct analytical data, run and interpreted in-house, and verified against history of prior batches.

    Many customers now expect not only compliance with ICH-Q3A/B for impurities, but also robust change control, often calling for full traceability to starting amino acids. This is not just about ticking regulatory boxes. Years of manufacturing have taught us that robust internal documentation preempts costly surprises. A deviation in input nitrogen source or Boc-anhydride quality that goes unnoticed can propagate through several generations of intermediates, especially when the end use is an API. Our standard process for Boc-D-Prolinol uses only high-purity D-proline, subject to incoming QC, reacted under monitored conditions with phase transfer catalysis to boost selectivity and minimize race-mate formation. Immediate quenching and thorough extraction keep unwanted hydrolyzed Boc byproducts to a minimum. Every synthesis trial, from R&D to 200-liter batches, follows this same attention to control.

    Why Prolinol’s Stereochemistry Sets the Pace

    Chirality is no theoretical concern for those of us preparing chiral auxiliaries and intermediates for the medicinal chemistry sector. We hear it often from feedback after customers have tried off-spec or racemized material from unstable supply chains: the headaches of ambiguous stereochemistry slow down entire programs. Boc-D-Prolinol, as we make it, starts with D-proline of confirmed optical purity, and by controlling pH, solvent choice, and temperature step by step, we keep racemization at bay.

    Every batch receives solid-phase IR, chiral HPLC analysis, and polarimetry—techniques that do more than assure compliance, they confirm the underlying trust that customers extend when planning multistep synthetic routes. In applications ranging from asymmetric catalysis to enantioselective ligand synthesis, the wrong enantiomer can halt project momentum. Over time we’ve found that many high-throughput discovery campaigns now favor protected amino alcohols like Boc-D-Prolinol because of their mix of functionality and stability. We look beyond just meeting chiral specs; maintaining a clean baseline for downstream coupling reactions often hinges on the removal of even trace racemized byproduct. That’s why batch-level scrutiny proves indispensable.

    Operational Experience: Lessons from the Production Line

    Every facility has stories about hiccups on the line—solvent pumps lag, temperature controllers fail, and the odd transfer line goes astray. Our track record didn’t grow out of a textbook, but out of the visible challenge of getting each lot right under all sorts of shifting global sourcing environments and regulatory landscapes. Scaling Boc-D-Prolinol for industrial use means constant attention to environmental health and safety, effluent capture, and operator training. We’ve faced scrutiny from regulatory reviewers; each time, maintaining detailed batch records and a commitment to transparency have been crucial.

    A real challenge is keeping moisture and air from affecting the product’s shelf life. Amino alcohols pick up water and CO2 fast in humid rooms, which can jeopardize both appearance and assay. We have invested in specialized drying and inert-atmosphere packaging, based on feedback from teams forced to re-dry or re-test before proceeding. All shipments, whether small sample or industrial lot, are packed under dry nitrogen, then stored at low temperature until delivery. It’s a small but critical step—skipping it only leaves problems for the next chemist down the line.

    Real Differences from Competing Protecting Groups and Intermediates

    We’ve seen the demand pattern shift from Fmoc to Boc protection, and many teams debate the advantages for their application. Boc-D-Prolinol’s particular value stems from its resilience—translating to robust protection under mild acid, ease of deprotection for late-stage modification, and compatibility across organic solvents. Where Fmoc-protection can lead to base-sensitive side products, Boc’s acid-labile properties make it preferable for multi-step or scale-up workflows. A key strength lies in the orthogonality; Boc groups weather conditions that might strip benzyl or tosyl protections, meaning downstream choices stay open. We keep records on failures in the field—accounts of incomplete deprotection in solid-phase synthesis or fouling caused by higher-molecular weight impurities in alternative intermediates. It’s these histories that keep us attentive to the details others might miss.

    The direct use of Boc-D-Prolinol for peptide-coupling chemistry, especially as a building block for unnatural amino acid incorporation, reveals differences less obvious on paper. Poorly controlled protection steps often yield byproducts that elude routine NMR scans. Process chemists and analysts have told us about unexplained NMR baseline noise or stubborn residues in flash columns that trace back to inferior starting material. By supplying batches traced to single-source production, we minimize these headaches. The focus remains on absolute enantiopurity and minimal residual salts, ensuring every gram works as hard as possible in the target reaction.

    Collaborative Development and Adaptation to Customer Feedback

    As a manufacturer, we never operate in isolation from the users of Boc-D-Prolinol. Process tweaks and incremental improvements result from thorough dialogues with end-users. Interactive QA sessions have driven us to refine baseline moisture limits and reconsider our in-plant drying protocols. Those running continuous processes, in particular, have asked for extended stability studies and easy-to-open packaging for glovebox transfer—a need we responded to with both improved containers and in-process stability checks.

    Some research partners have called for higher analytical resolution, seeking detailed impurity profiles to feed into their IND filings or route optimization. Working directly helps highlight the reality: no two synthetic schemes put the same demands on an intermediate. By committing staff chemists to tailor analytical approaches, from HRMS down to trace inorganic analysis, we support those stretching Boc-D-Prolinol’s performance envelope on the frontier of molecular design.

    Pushing Toward Sustainability and Safer Manufacturing

    With international focus on green chemistry, our own plant practices evolve as new solvents, reagents, and purification methods arise. Boc-D-Prolinol synthesis, historically dependent on chlorinated solvents and traditional phase-transfer catalysts, now sees greener alternatives in select steps. We know the trade-off between yield, selectivity, and environmental footprint shapes process priorities, especially as customers factor in regulatory compliance on waste handling. New assets, like closed-loop solvent recycling and on-site wastewater treatment, started as costly investments but now support both sustainability and cost control over time.

    Operator safety has also become central. Each lot of Boc-D-Prolinol interacts with process hazards—heat, pressure, and often the sharp odor of evolving isobutylene. We mandate protective measures not only for our people but to reduce downstream hazard to our customers. Many of our production advances—like transitioning to dust-free milling or enclosed transfer systems—came from fielding direct worker feedback about previous bottlenecks on the line.

    The Manufacturer’s View: Value Grows from Accountability

    Supplying Boc-D-Prolinol goes far deeper than shipping a parcel on schedule. We’ve expanded capacity as demand climbed, but the core value remains: whoever uses the intermediate next can depend on its performance, whether that means sharp melting point, consistent color, or the absence of obscure byproducts that could haunt a tedious purification sequence. Our responsibility follows every kilogram, wherever it ends up: discovery lab or GMP-compliant environment, every lot receives the same tracing, the same batch-level controls.

    With a horizon growing to more complex, chiral-targeted molecules, the feedback loop between manufacturer and chemist intensifies. That’s why every year, we revisit not only the technical parameters of our Boc-D-Prolinol but also the broader practices underlying our operation—auditing supply lines, adopting green chemistry advances, and investing in the analytical and process infrastructure that ultimately delivers peace of mind to our customers.

    Supplying Boc-D-Prolinol feels as much about building trust as it does about process chemistry. We bring decades of hands-on learning, a stubborn commitment to continual improvement, and a transparent approach that welcomes customer questions—no matter how technical or specific. That’s how we keep pushing, batch after batch, to deliver not only a reagent but also the reliability and certainty that comes from a partner truly invested in your next successful synthesis.