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(S)-1-Benzyl-3-Pyrrolidinol

    • Product Name (S)-1-Benzyl-3-Pyrrolidinol
    • Alias (S)-1-Benzylpyrrolidin-3-ol
    • Einecs 642-019-7
    • 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

    957845

    Name (S)-1-Benzyl-3-Pyrrolidinol
    Iupac Name (S)-1-benzylpyrrolidin-3-ol
    Molecular Formula C11H15NO
    Molecular Weight 177.24 g/mol
    Cas Number 137981-74-5
    Smiles C1CN(C[C@@H]1O)Cc2ccccc2
    Appearance White to off-white solid
    Optical Activity S-configuration (chiral center at C3)
    Solubility Soluble in organic solvents (e.g., DMSO, methanol)
    Storage Temperature Store at 2-8°C
    Synonyms (-)-1-Benzyl-3-pyrrolidinol

    As an accredited (S)-1-Benzyl-3-Pyrrolidinol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle containing 25 grams of (S)-1-Benzyl-3-Pyrrolidinol, with tamper-evident cap and clear hazard labeling.
    Shipping (S)-1-Benzyl-3-Pyrrolidinol is shipped in sealed, chemical-resistant containers to prevent contamination and moisture exposure. Packages are labeled per regulatory guidelines, including hazard identification if applicable. The chemical is transported under controlled conditions, often at ambient temperature, and handled by certified carriers to ensure safe and compliant delivery.
    Storage (S)-1-Benzyl-3-pyrrolidinol should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep at room temperature, preferably between 2–8°C (refrigerated), and avoid moisture exposure. Properly label the container and ensure compliance with standard laboratory chemical storage protocols.
    Application of (S)-1-Benzyl-3-Pyrrolidinol

    Applications of (S)-1-Benzyl-3-Pyrrolidinol in Industrial Manufacturing

    (S)-1-Benzyl-3-Pyrrolidinol finds consistent demand in advanced chemical industries due to its enantiopure configuration and functional groups. We strictly supply this chiral intermediate to manufacturers operating in tightly regulated downstream sectors with stringent requirements on purity, traceability, and batch reproducibility.

    1. Chiral Pharmaceutical Intermediate Synthesis

    Pharmaceutical formulation groups use (S)-1-Benzyl-3-Pyrrolidinol in the synthesis of chiral intermediates for targeted APIs, especially CNS-active drug candidates and advanced analgesic substances. Its defined stereochemistry supports high-yield enantioselective hydrogenation and reductive amination steps. We supply a controlled material that simplifies enantiomeric separation and reduces downstream purification. Our industrial partners have integrated this intermediate as a building block for new molecular entities destined for clinical pipelines.

    Industry compliance standards

    • ICH Q7: Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU EudraLex Volume 4, Part II: GMP for APIs
    • USP General Chapters — Chiral Purity
    • 21 CFR Part 210/211: US Pharmaceutical Manufacturing Controls

    Typical usage ratio

    • Batch processes range from 1 mol-% to 15 mol-% depending on route and targeted enantiomeric excess. Chemists adjust loading according to the API's chiral core and reaction kinetics.

    Downstream process integration

    • Intended for use in the early to mid-stage route, entering during Grignard reactions, asymmetric hydrogenation, or reductive amination as a chiral source. Isolated crude or purified product sent onward under GMP containment.

    Final product types

    • API enantiomers (preclinical, clinical, and commercial scale drugs)
    • CNS-active intermediates
    • Analgesic molecular scaffolds
    • Chiral auxiliaries used in stereospecific synthesis

    2. Agrochemical Synthesis for Selective Herbicides

    Global crop protection formulators incorporate (S)-1-Benzyl-3-Pyrrolidinol into the synthesis of certain classes of heterocyclic selective herbicide actives. The chiral configuration plays a key role in establishing herbicidal activity and environmental persistence profile. We partner with agrochemical process teams to deliver enantiopure raw material for efficient coupling steps, reducing formation of racemic byproducts and minimizing downstream purification challenges.

    Industry compliance standards

    • FAO/WHO Manual on Development and Use of FAO and WHO Specifications for Pesticides
    • OECD Series on Pesticides – Test Guidelines for Metabolites
    • ISO 9001:2015 Quality Management for Chemical Inputs
    • REACH Regulation (EC) No 1907/2006 (for EU registration)

    Typical usage ratio

    • Concentration typically set at 2–8 wt% based on the designed coupling or ring-closure step. Adjusted to match active loading and target impurity profile.

    Downstream process integration

    • Deployed in building key pyrrolidine-based herbicidal actives during late-stage condensation or nucleophilic substitution. Used in both batch and continuous feed reactors with in-process assay monitoring.

    Final product types

    • Chiral herbicide technical concentrates
    • Formulated crop protection products (emulsifiable concentrates, SCs)
    • Pre-mix herbicidal granules containing heterocyclic motifs
    • Herbicide active ingredient standard solutions for regulatory submission

    3. Specialty Fine Chemicals for Chiral Catalysts

    Producers of asymmetric catalysts deploy (S)-1-Benzyl-3-Pyrrolidinol when preparing ligand backbones for use in enantioselective catalytic systems, including hydrosilylation and transfer hydrogenation. The compound’s stereochemical integrity supports high activity and selectivity in ligand design, benefiting manufacturers scaling up high-value fine chemical transformations.

    Industry compliance standards

    • ISO 80000-9:2019 Chemical Quantities (for catalyst purity assay)
    • EN ISO/IEC 17025 Laboratory Accreditation
    • Responsible Care® Global Charter
    • Chemical Facility Anti-Terrorism Standards (CFATS, US) for specialty chemicals

    Typical usage ratio

    • Integrated at 0.5–3 eq. per metal center in ligand backbone formation. Chemists optimize based on required catalyst turnover and selectivity in downstream transformations.

    Downstream process integration

    • Fed into ligand assembly reactors after metal precursor addition, followed by characterisation and scaling tests. Downstream, catalysts undergo solution blending and packing into standard containers.

    Final product types

    • Homogeneous chiral ligands
    • Asymmetric hydrogenation catalysts
    • Custom catalytic systems for planned fine chemical synthesis
    • Ligand libraries for process R&D

    4. Advanced Materials for Electronic Chemicals

    Chemical engineers working in semiconductor and optoelectronic component manufacturing exploit (S)-1-Benzyl-3-Pyrrolidinol as a chiral functional group donor or crosslinking intermediate. The material supports assembly of specialty polymers and photoresists which demand high enantiopurity and batch reproducibility. Our production supports supply for integration into precursor lines governed by strict electronics sector standards.

    Industry compliance standards

    • SEMI C1 Specification for Materials for Microelectronics
    • IPC-4552A: PCB Surface Quality Testing
    • RoHS Directive (EU 2011/65/EU)
    • ISO 14001:2015 Environmental Management for Chemical Handling

    Typical usage ratio

    • Blending ratio spans 0.1–2 wt% in copolymer backbones or additive streams, depending on target resist thickness and chiral property imparted. Adjusted in pilot runs in line with end-use film requirements.

    Downstream process integration

    • Introduced during polymerisation or resist formulation step, before filtration and coating. Electronic grade filtration and in-line QA monitoring verify contaminant levels are within electronic application limits.

    Final product types

    • Photoresists for integrated circuit fabrication
    • Chiral specialty polymers for optoelectronic devices
    • Micro-patterning materials
    • Electronic substrate treatments
    Free Quote

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    Certification & Compliance
    More Introduction

    Introducing (S)-1-Benzyl-3-Pyrrolidinol: The Next Step in Pyrrolidine Chemistry

    At our manufacturing site, we see (S)-1-Benzyl-3-Pyrrolidinol make a difference every day, not only in production lines but also in hands-on synthetic work. We pour decades of chemical synthesis experience into producing this compound, refining purity and chiral fidelity beyond what generic supply can reach. Our chemists stand behind each batch because direct involvement throughout every stage gives us the type of control that chemical traders simply can’t hope to match.

    The Model: Consistency in Chiral Synthesis

    (S)-1-Benzyl-3-Pyrrolidinol embodies a leverage point in asymmetric synthesis. We tailor our methodology to favor the (S)-enantiomer by using precise catalytic steps and strict temperature control, since any deviation at this scale breaks the reliability high-end research demands. Unlike racemic materials that require chiral resolution downstream, our enantioselective process takes stress off later synthesis steps and cuts unnecessary waste. This focus keeps our product popular for both small molecule drug research and specific agrochemical development where enantioselectivity dictates downstream function.

    Specifications Grounded in Real-World Use

    You won’t find us hiding behind vague terms. Every lot of (S)-1-Benzyl-3-Pyrrolidinol ships with comprehensive data—enantiomeric excess verified by chiral HPLC, NMR spectra, and complete impurity profiles. Based on our customer conversations, we set our minimum specification for enantiomeric purity at >99%. We routinely analyze water and residual solvents at low ppm, since moisture and volatile residues can disrupt downstream Grignard or reductive amination steps. Clarity in specifications means process chemists know exactly what they’re working with; consistency from bottle to bottle means scale-ups have fewer surprises.

    We see requests for different grades: research, pilot plant, and full-scale GMP intermediates. Different clients want different things from us. Those in discovery chemistry often prefer a fast turnaround with smaller lots; production engineers working toward validation demand rigorous documentation and traceability. Both come to us because our in-house process reduces cross-contamination and batch drift. By retaining full control from starting materials through purification, we ensure you never need to recalculate for changing impurities.

    Applications: Why Industry Demands Chiral Fidelity

    The core of (S)-1-Benzyl-3-Pyrrolidinol’s relevance comes from its versatility in medicinal and specialty chemistry. Research labs use it as a resolving agent, a protected pyrrolidine scaffold, and a starting point for building more complex chiral amines and alcohols. This intermediate serves as a linchpin in enantioselective syntheses, enabling downstream construction of pharmacophores and advanced heterocycles. The benzyl group offers both protection during multi-step synthesis and a functional handle for late-stage modifications.

    We’ve worked with teams developing novel CNS therapeutics who specifically need the (S)-enantiomer for receptor selectivity. Others approach us for its utility in constructing intermediates for custom ligands and natural product analogues. Compared with generically protected alcohols or unprotected pyrrolidines, this compound saves steps and improves yield. Process R&D chemists tell us removing chiral resolution steps unlocks better atom economy, translating directly into faster drug development and less organic waste.

    Some clients pursue SAR studies where rapid access to analogs matters. Single-enantiomer supply from the outset streamlines their library synthesis—each member benefits from a defined stereocenter, and subsequent transformations track with fewer side-products. Those working on process scale-up appreciate the minimal regulatory burden: manufacturing direct from our product means fewer corrective filings or specification back-and-forth. The fact we control our own process from start to finish means analytical results arrive with the credibility required for repeatable, compliant documentation.

    Standing Apart: What Hands-On Manufacturing Really Means

    While many lab supply catalogs will list (S)-1-Benzyl-3-Pyrrolidinol, the real difference emerges from how it’s made and who stands behind it. We synthesize, purify, and characterize every batch under the same roof. This isn’t about marketing phrases—it’s how we know our intermediates remain free from excess byproducts, such as overalkylated pyrrolidines, unreacted benzyl chloride, or chiral inversion.

    Through years of handling sensitive intermediates, we’ve modified our workflow to minimize racemization—adjusting hydrogenation conditions and using selective oxidants during workup. Our chemists fine-tuned cooling and seeding protocols, limiting epimerization during key reductions. Where other suppliers may take shortcuts or outsource steps, every transformation happens in our reactors, under our oversight.

    Some customers have shared frustrations about inconsistent melting points or solvent residues from prior vendors. In our line, a logic-driven, experienced approach stops these problems: we validate our purification routinely at the bench, not just through paperwork. Each campaign includes control runs at micro and kilo scale, so we catch solvent carryover or crystallization drift before it enters your supply chain.

    Scaling presents its own headaches. Large lots often magnify minor deviations in enantiomeric purity. To anticipate this, we designed our reactors and filtration systems to avoid dead spots and cross-contamination. We maintain dedicated lines for sensitive chiral intermediates like (S)-1-Benzyl-3-Pyrrolidinol, both for in-process sampling and for aseptic packaging. This kind of infrastructure doesn’t happen overnight; it comes from a clear recognition of what quality really means for downstream chemists.

    Addressing Real World Issues: Stability and Transport

    Not every intermediate travels well—some break down or lose purity en route. With (S)-1-Benzyl-3-Pyrrolidinol, we invested in stability studies at ambient and sub-ambient conditions. Moisture pick-up and oxidative degradation narrow the handling window; we tackled this by using nitrogen-flushed, amber glass containers, and adding desiccant pouches for larger shipments.

    Our warehouse team trains specifically on these more sensitive lots, ensuring temperature logs accompany long-distance shipments. In cases requiring extended storage, we offer smaller, sealed packs to minimize opening frequency. Experience taught us to flag certain shipping lanes where delays threaten stability; close contact with logistics partners helps bypass these pitfalls. For onsite storage, we offer guidance on refrigeration and inert gas backfill, rooted in direct shelf-life data.

    Continuous Improvement: Listening to Chemists

    We believe close feedback between manufacturer and end-user leads to better chemistry. Over the past decade, process engineers and research chemists have shaped tweaks to our isolation and packaging. For one API developer, we reformulated a final purification step to limit trace byproducts that interfered in a downstream hydrogenation. Another biotech group requested granular batch data for regulatory submission; our QC team started including validated chiral HPLC overlays with every shipment.

    Patterns emerge through these conversations. Big differences start in the granular details. We do not rely on standard spec sheets that never get updated; practical experience guides each revision. If a chemist struggles with crystallization, our process team can advise on solvent selection, filtration rates, and drying protocols—based entirely on hands-on batch work. These continuous refinements help every lot of (S)-1-Benzyl-3-Pyrrolidinol function as reliably in process scale as it does in the R&D lab.

    Differentiation: Not All Pyrrolidinols Are Created Equal

    A technical bulletin won’t cover the nuances that set (S)-1-Benzyl-3-Pyrrolidinol apart. Structurally, the benzyl group offers both chemical protection and a functional point for elaboration, which distinguishes it from simple N-unsubstituted pyrrolidinols and their less reactive profiles. Many alternative pyrrolidinols lack the stereocontrol required for advanced synthesis, forcing downstream chromatographic purification or costly chiral resolution. With our product, the handedness comes built-in, eliminating extra steps and potential inversion.

    The (S)-enantiomer, in particular, aligns with the stereochemistry found in key drug frameworks and natural product scaffolds. Some suppliers opt for a racemic approach for cost reasons, passing resolution onto downstream users. We stay committed to single-isomer output because chemists trust this profile when planning scale-up for a multi-kilo API or high-throughput lead generation project.

    From a technical standpoint, we see less N-debenzylation required for further modification, along with fewer oxidative side reactions—especially when compared to unsubstituted analogs. Process safety improves, since fewer hazardous reagents are worked up and less toxic byproduct forms. Customers working under tight environmental or regulatory protocols benefit from this leaner synthesis, reporting fewer permit headaches and waste disposal concerns.

    Supporting Sustainable Synthesis

    We treat green chemistry both as a requirement and a point of pride. Years ago, we overhauled our route to use milder bases and catalytic hydrogenation, ditching stoichiometric metal reagents wherever possible. Our production lines recycle solvents and capture mother liquors, reducing total hazardous output. We document our carbon footprint at every campaign scale, responding to increasing pressure from regulatory bodies and internal policy shifts at client organizations.

    Pharmaceutical and biotech customers ask for lifecycle documentation and data on upstream precursor sourcing. Our supply chain team worked directly with raw material suppliers to validate their own compliance. From procurement to packaging, we know exactly which barrels and drums contributed to each final lot; traceability helps build transparency and accountability at every step.

    Working with real, hands-on chemists taught us the urgency of meeting these transparency standards—whether for regulatory submissions or internal audits. In response, we deliver full documentation tracing synthesis, purification, storage conditions, and quality data for every shipment. This system cuts risk, strengthens compliance-ready records, and delivers peace of mind to those who use our (S)-1-Benzyl-3-Pyrrolidinol as a foundation for high-value products.

    Field Experience: Troubleshooting and Real-World Solutions

    Not every process goes smoothly; experience teaches where pitfalls arise. Some partners have run into emulsion issues in aqueous workup, especially at larger scale when phase transfer doesn’t perform as expected. Based on what our process team learned, we now recommend slight modifications in salt handling and cooling to sharpen layer separation. In cases of unanticipated solid formation, adjusting antisolvent ratios on-site has helped maximize yield without raising impurity content.

    Chiral integrity sometimes suffers under harsh conditions; a handful of users have flagged slippage after moving to higher pressure or prolonged exposure to acidic reagents. Our QC crew now inserts check-points at stages known to stress the chiral center and, if asked, can supply full guidance for downstream purification. It is this cycle—factory to bench to pilot plant and back—that lets our (S)-1-Benzyl-3-Pyrrolidinol fill a critical, trustworthy role in advanced synthesis.

    Looking Ahead: Why Control Matters in Advanced Chemistry

    Direct manufacturer involvement makes an enormous difference both in quality and in the kind of problem-solving that brings value to the chemists at the bench. We see a future where single-enantiomer intermediates like (S)-1-Benzyl-3-Pyrrolidinol become the standard, not the exception. Outsourced supply chains hand off risk and responsibility; in our operation, chemists take charge from start to finish. This commitment shortens lead times, improves purity, and brings transparency all the way through the synthesis process.

    We invite our partners to connect directly—not just by email or spreadsheet, but side by side if needed, to solve problems as they arise. Observing production up close, clients gain confidence: they see each step, understand each safeguard, and appreciate the experience that comes from handling unstable intermediates, batch after batch. With each challenge, our team grows more adept at balancing speed and safety, documentation and innovation.

    We believe the path forward in chemical manufacturing runs through transparency, collaboration, and a willingness to adapt processes as scientific demands change. For all these reasons, (S)-1-Benzyl-3-Pyrrolidinol—when made right—opens new possibilities not only in research, but in reliable, sustainable, and safe process chemistry. It is the product of experience, guided by daily feedback from the field and by a fundamental respect for the chemist’s craft.