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1-Benzylpyrrolidin-3-Yl-Methanol

    • Product Name 1-Benzylpyrrolidin-3-Yl-Methanol
    • Alias 3-(Hydroxymethyl)-1-benzylpyrrolidine
    • Einecs 674-800-6
    • 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
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    Specifications

    HS Code

    236795

    Chemical Name 1-Benzylpyrrolidin-3-yl-methanol
    Molecular Formula C12H17NO
    Molecular Weight 191.27 g/mol
    Cas Number 128424-44-2
    Appearance White to off-white solid
    Solubility Soluble in organic solvents such as DMSO and methanol
    Storage Conditions Store at 2-8°C, in a dry and cool place
    Purity Typically ≥ 98% (variable by supplier)
    Structure Type Pyrrolidine ring substituted at positions 1 (benzyl) and 3 (methanol)
    Iupac Name 1-benzylpyrrolidin-3-ylmethanol
    Smiles OC[C@@H]1CCN(Cc2ccccc2)C1

    As an accredited 1-Benzylpyrrolidin-3-Yl-Methanol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 1-Benzylpyrrolidin-3-Yl-Methanol, 25g, packaged in a sealed amber glass bottle with tamper-evident cap and detailed hazard labeling.
    Shipping 1-Benzylpyrrolidin-3-yl-methanol is shipped in tightly sealed, clearly labeled containers to ensure safety and stability during transit. Packaging complies with chemical safety regulations. The chemical is protected from moisture, heat, and direct sunlight. Shipping documentation includes hazard and handling instructions, and package integrity is maintained to prevent leaks or accidental exposure.
    Storage 1-Benzylpyrrolidin-3-yl-methanol should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Use tightly sealed containers made of compatible materials to prevent contamination or evaporation. Clearly label the storage container, and keep it away from sources of ignition and moisture. Store under recommended temperature conditions, typically at room temperature.
    Application of 1-Benzylpyrrolidin-3-Yl-Methanol

    Applications of 1-Benzylpyrrolidin-3-Yl-Methanol in Industrial Manufacturing

    1-Benzylpyrrolidin-3-Yl-Methanol plays a strategic role as a specialty intermediate for advanced synthesis routes. It serves key pharmaceutical and fine chemical sectors, particularly where precise chiral building blocks and functional groups are required for end-product efficacy and regulatory compliance. As a direct manufacturer, we supply this material for critical process stages across multiple downstream manufacturing fields.

    1. Chiral Pharmaceutical Intermediate Synthesis

    Pharmaceutical producers source 1-Benzylpyrrolidin-3-Yl-Methanol as a stereochemically defined intermediate for constructing active pharmaceutical ingredient (API) scaffolds, including CNS drugs and second-generation hypertensives. Its chiral center facilitates enantioselective syntheses, especially in steps requiring reductive amination or Grignard reactions for active fragment installation. Strict documentation and traceability ensure the material’s suitability in cGMP-compliant operations.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • FDA 21 CFR Part 210/211 (Finished Pharmaceuticals)
    • European Pharmacopeia (Ph. Eur., Monograph 2.2.46)
    • USP–NF General Notices & Requirements for Intermediates

    Typical usage ratio

    • Between 0.5 and 1.5 molar equivalents per synthetic batch, scaled based on desired API volume and yield optimization; adjustment depends on target product and route complexity.

    Downstream process integration

    • Introduced after initial ring formation, entering at fragment coupling or enantioselective modification step; dosing completed under nitrogen, followed by in situ derivatization or direct condensation under GMP process controls.

    Final product types

    • Antipsychotic medication active ingredients
    • Antidepressant pharmaceutical actives
    • Beta-adrenergic antagonists
    • Custom chiral building blocks for contract synthesis

    2. Fine Chemical Synthesis for Agrochemical Intermediates

    Crop protection R&D teams employ 1-Benzylpyrrolidin-3-Yl-Methanol as a precursor when engineering agrochemical agents, including fungicidal and herbicidal actives with nitrogen-containing heterocycles. It supports high selectivity for target isomers in multi-step processes involving alkylation or acylation, meeting demands for minimized byproducts and strict impurity profiling.

    Industry compliance standards

    • ISO 9001:2015 Quality Management for Fine Chemical Manufacturing
    • FAO/WHO Pesticide Specifications (FAO Manual, Part One, Section 4)
    • REACH Regulation (EC) No 1907/2006 for Agrochemical Substances
    • OECD GLP (Good Laboratory Practice) for Analytical Process Validation

    Typical usage ratio

    • 0.8–1.3 molar equivalents, adjusted according to the complexity of heterocycle integration and desired pesticide purity; formulation labs calibrate ratios via small-scale pilot studies.

    Downstream process integration

    • Fed into mid-stage synthetic blocks, incorporated under anhydrous conditions into stepwise reactions; subjected to post-reaction workup, including solvent exchange and crystallization, to maintain activity and purity.

    Final product types

    • Heterocyclic pesticide precursors
    • Selective fungicidal agents
    • Herbicide active intermediates
    • Custom agrochemical screening compounds

    3. Specialty Resin Modifier for Polymer Production

    Polymer and epoxy manufacturers utilize 1-Benzylpyrrolidin-3-Yl-Methanol as a functional monomer modifier to influence ring structure, flexibility, and cross-link density in high-performance resin systems. This intermediate supplies reactivity for customizing thermal and mechanical properties, essential in electronics-grade and specialty coating resins where end-use demands continuous stability and strict VOC thresholds.

    Industry compliance standards

    • ISO 9001:2015 for Specialty Polymer Production
    • RoHS (Restriction of Hazardous Substances in Electronics)
    • EPA TSCA requirements on New Chemical Substances
    • UL 94 Flammability Testing for Plastics

    Typical usage ratio

    • 1–5% weight of resin system, determined based on required cross-linker reactivity; higher ratios boost thermal resistance, while lower percentages maintain flexibility.

    Downstream process integration

    • Mixed directly into resin pre-polymerization feed; combined under active stirring with initiators and co-monomers prior to controlled temperature-curing cycles to achieve target network structure.

    Final product types

    • Electronics encapsulation resins
    • Low VOC coatings for industrial substrates
    • High-temperature resistant adhesives
    • Custom structural polymer blocks

    4. Precursor in Custom Fragrance and Aroma Compound Synthesis

    Fragrance manufacturers employ this material as a synthetic intermediate when building complex aroma compounds with piperidine or pyrrolidine motifs, integrating it into reaction sequences that require precise positioning of benzyl and hydroxy functional groups. Strict batch documentation allows full traceability for downstream blending and IFRA compliance.

    Industry compliance standards

    • IFRA Standards for Fragrance Ingredient Safety (current amendment)
    • EU Cosmetic Regulation (EC) No 1223/2009 for Ingredient Control
    • ISO 9235:2013 (Aromatic Natural Raw Materials & Derivatives)
    • RIFM Safety Evaluations for Fragrance Ingredients

    Typical usage ratio

    • 0.05–0.5 molar equivalents in target aroma compound constructions; formulation teams tune input based on desired olfactory note intensity and blending characteristics.

    Downstream process integration

    • Entered after initial skeleton assembly, used in key functionalization steps and finally isolated via fractional distillation to remove unreacted intermediates, before transfer to compounding facilities.

    Final product types

    • Specialty aroma intermediates
    • Pharma-grade fragrance components
    • Cosmetic-grade perfume concentrates
    • High-value flavor and fragrance synthons

    5. Research Chemical Synthesis and Reference Standard Preparation

    Analytical laboratories and research institutes rely on 1-Benzylpyrrolidin-3-Yl-Methanol as a controlled precursor for synthesizing labeled reference substances and analytical standards, particularly in forensic and bioanalytical method development. Sourcing from a manufacturing origin ensures batch consistency, with full documentation and stability data supporting accreditation under GLP and ISO standards.

    Industry compliance standards

    • ISO 17025:2017 Requirements for Testing and Calibration
    • OECD Good Laboratory Practice Principles
    • FDA Guidance for Industry: Bioanalytical Method Validation
    • Traceability to NIST Reference Materials

    Typical usage ratio

    • 0.01–0.1 molar equivalents for micro-scale syntheses; method developers optimize scaling based on analytical assay sensitivity and target labeling efficiency.

    Downstream process integration

    • Charged at milligram-to-gram scale in custom glassware; often subjected to isotopic labeling, subsequent functional group modification, and high-purity purification via preparative HPLC before repository storage.

    Final product types

    • Analytical reference standards
    • Labeled substance controls
    • Research-use chemical intermediates
    • Custom synthesized standard solutions
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    Certification & Compliance
    More Introduction

    Introducing 1-Benzylpyrrolidin-3-Yl-Methanol: A Manufacturer’s Perspective

    Decades of Experience, Straight from the Production Floor

    Having produced specialty chemicals for over two decades, we understand the complex demands that researchers, pharmaceutical formulators, and advanced material chemists bring to our door. Our team has taken time to fine-tune each stage of the 1-Benzylpyrrolidin-3-Yl-Methanol process, leveraging real feedback from actual users—not just lab tests. Over the years, our customers, many of whom we know by name, return to us with precise requests for purity, particle properties, and reliable batch-to-batch consistency. They’ve tested the alternatives, and every time, they’ve come back to us with a story or a question. For us, the conversation about 1-Benzylpyrrolidin-3-Yl-Methanol always starts with application, then moves to performance.

    Understanding the Role of 1-Benzylpyrrolidin-3-Yl-Methanol

    In our own production lines, we see this compound used most intensively in complex pharmaceutical intermediates and in fine chemical synthesis where stereochemistry and side-reaction control are critical. Common requests involve tight control of alcohol to pyrrolidine derivatives, and customers often look to us because they know we monitor every variable from source materials to packaging. Many larger suppliers may emphasize generic grades, but our emphasis lands solidly on the process. Every batch, no matter the order size, gets hands-on attention by trained staff who have watched this molecule’s manufacture go from research scale to tonnage batches.

    Unlike standard pyrrolidine derivatives, the benzyl substitution and alcohol group complicate synthesis, storage, and handling. Temperature-sensitive logistics keep us honest, making sure packaging lines run with precise controls to avoid moisture ingress or light degradation. What seems simple on paper ends up much more demanding when meeting client deadlines and analytical targets. On the shop floor, we keep our routines tight at key points, remembering that this product will directly influence someone’s next set of trial results or scale-up runs.

    Importance of Purity and Consistency

    Analytical chemistry underpins our work with this compound. We rely on validated analytical methods—mainly NMR, HPLC, and mass spectrometry—to guarantee every shipment matches customer specifications. Small impurity shifts may undermine entire synthesis routes downstream. Technicians run comparative checks against certified reference materials curated in-house. Years back, we encountered a run of inconsistent chromatographic peaks—less than two percent variance—but experienced chemists caught it long before delivery. Problems identified in advance save headaches for everyone down the line, and that sort of discipline grows only from repeated exposure to real-world challenges.

    Some newer entrants to the market treat this molecule as a routine product. They might gloss over storage conditions or shortcut drying protocols. If you’ve ever tried to work with an off-color or slightly oxidized batch, you know how difficult it can be to get reproducible results. Our plant foremen encourage extra caution when monitoring off-gassing and humidity within packaging runs. This may seem excessive, but it grew out of hard lessons and costly mistakes during our own early years of manufacturing. Reliable 1-Benzylpyrrolidin-3-Yl-Methanol, as we ship it today, reflects a decade’s worth of improvements, sometimes driven by a single customer’s hard-won experience.

    Specifications and Real-World Requirements

    Customers ask about specifications—that’s a given. Our experience has shown a strong market preference for purity levels above 98 percent, as even minor impurities can create headaches in end-use synthesis, particularly in medicinal chemistry projects. We field daily technical inquiries about melting point ranges, moisture content, appearance, and storage stability. Instead of defaulting to published ranges, we always cross-check batches near shipment, re-confirming the numbers using our own protocols rather than relying solely on theoretical values or generic supplier sheets.

    Some colleagues in the field have suggested the extra verification steps eat into margins, but our approach has proven itself in the long haul. Reports of failed reactions based on marginal materials have prompted us to double down on this practice. Put simply, our clients run tight synthesis schedules, and even a slight error in starting material purity can snowball into weeks of backtracking. This is where deep experience in specialty chemical production cycles becomes invaluable.

    Usage Patterns: Direct Feedback from Our Client Base

    On the application side, this molecule features across a range of reactions, but we see it especially favored in chiral pool syntheses and in the construction of C–N and C–O bonds where stereochemistry carries downstream implications. Researchers working on central nervous system (CNS) active compounds, or multi-step synthesis programs, depend on access to this compound with no surprises batch-to-batch. We track which industries show recurring orders—pharmaceuticals, custom synthesis houses, and biochemistry labs.

    Direct feedback often points to issues encountered with outsourced suppliers, usually related to over-extended supply chains, questionable quality control, or poorly documented batches. Once, a client came to us after three failed pilot-scale campaigns with another vendor; they had discovered subtle batch contamination that stymied their end-product performance. We worked with this customer to reconstruct their process point-by-point, adjusting our protocols for their targeted needs and eventually salvaging their development timeline. Such cases highlight why real, on-the-ground manufacturer support makes a difference.

    How This Product Differs from Other Pyrrolidine Derivatives

    With years spent producing both standard pyrrolidine derivatives and their more functionalized analogs, we notice immediate chemical and processing differences. 1-Benzylpyrrolidin-3-Yl-Methanol introduces both a benzyl moiety and a primary alcohol onto the pyrrolidine core. From a process standpoint, these modifications require different handling compared to simpler ring systems—solubility, reactivity, and storage sensitivity must be accounted for early on in the synthesis and packaging plans.

    In practice, standard pyrrolidines endure longer storage with fewer issues. The added benzyl group, on the other hand, increases molecular weight and hydrophobicity, creating opportunities in solid-phase synthesis and medicinal scaffolds, but also introducing purification challenges. The methanol group affects both hydrogen bonding and downstream reaction scope, especially in asymmetric synthesis or chiral catalyst development. Our customers rely on these molecular distinctions when selecting materials that best match their synthetic strategy.

    Manufacturing this compound stretches technical capabilities, as the combination of substituents forces careful planning on choice of solvents, reaction controls, and purification strategies. Push too hard on temperature or ignore moisture controls, and you end up with non-reproducible color or purity outcomes. In our earlier years, we learned this the hard way—lost a week of production when a routine filtration was performed under suboptimal atmospheric controls. Since then, we have adopted strict engineering controls all the way to packaging, ensuring stability and traceability through each customer order.

    Supporting Sustainable and Transparent Supply Chains

    These days, questions of sustainability and traceability come up almost as often as technical details. We have responded by switching to renewable feedstocks and setting up full traceability reports from raw materials through to shipped finished goods. This is no small undertaking, especially in a busy, multi-product facility. We’ve partnered with suppliers willing to certify every step of their own production, which builds assurance for our own clients that no blind spots exist in their sourcing chain.

    Our on-site quality managers now maintain dedicated records for each raw material input, along with process documentation that auditors can check at a moment’s notice. External inspections have provided useful feedback, though the greater benefit has come in the form of long-term trust with clients concerned about regulatory requirements or environmental targets. This approach creates honest oversight, both internally and externally, which we see reflected in steady, repeat customer relationships.

    We also invest in proper waste handling and emissions monitoring, directly tracking solvent use, energy input, and byproduct generation. A few years ago, we installed secondary containment on key reactors and new solvent recovery infrastructure. Such improvements rarely register in standard product descriptions, but they matter for the long-term reliability and safety of our operations.

    Real-World Problem Solving for End-Users

    Technical support forms the second half of what makes our 1-Benzylpyrrolidin-3-Yl-Methanol successful downstream. Clients reach out when small anomalies show up in their reactions—a shift in ghost peaks on HPLC, or variance in solubility and reactivity. Our lab team is trained to reverse-engineer these findings. Often, the trouble traces back to a minor impurity or a variation in the moisture profile. We can pull from our in-house spectra archives—years of cumulative batch records—to confirm at what stage a deviation appeared.

    Early on, one pharmaceutical developer flagged a drop-off in product yield linked to seemingly trivial changes in our methanol content. They shared a full roll-out history of their process, which, in turn, prompted us to introduce tighter vacuum drying and immediate post-packing sealing. This collaboration style typifies the best outcomes from chemical manufacturing partnerships, as solutions emerge from hands-on evidence, not just from generic advice or theoretical guidance.

    Lessons Learned from Continuous Improvement

    Every chemical manufacturer faces setbacks, but experience sharpens protocols and teamwork. Our journey with 1-Benzylpyrrolidin-3-Yl-Methanol has been shaped by a constant risk-and-learn cycle. We refined reactor setup procedures after noticing that trace nickel impurities from processing equipment contributed unwanted side reactions. Adopting inert-lining and performing bonus swab tests on reactors addressed the issue and provided value to our clients whose work would otherwise have been jeopardized.

    We also learned that real progress comes from integrating every team—from plant operators to analytical chemists—into the improvement loop. Everyone has hands-on exposure to process setup and troubleshooting. This fosters a shared ownership mentality, making it easier to push for quality upgrades that pay off during scaling up or when supporting clients with atypical needs.

    Through joint troubleshooting with chemists at academic labs and pharmaceutical innovators, we continually re-examine our parameters and fine-tune them for optimal performance. This regular challenge and review culture also motivates us to experiment with greener solvents and drop residual traces to levels that outpace standard benchmarks.

    Addressing Supply Chain Reliability

    Perhaps the most significant challenge in recent years has been supply chain interruptions triggered by global events. Delays affect our schedules just as much as our customers’ research timelines. Having always maintained in-house stock and managing multiple validated sources for critical precursors, we routinely buffer our system against market shocks. No one gets served by a just-in-time inventory if new batches face port delays or customs holds.

    In the heat of a sudden disruption, our in-house ability to custom-synthesize smaller lots keeps committed orders moving. Such flexibility only develops with direct manufacturing capacity, not brokerage. As a result, customers with ongoing development projects usually prefer working with us since they see our reliability in action.

    One strategic client recently thanked us for this ability to maintain supply during a regional export ban that froze other shipments. The trust and continued partnership go well beyond transactional relationships, extending into joint planning for future supply resilience.

    Why Working With Manufacturers Directly Matters

    Over years of running our own production facilities, we’ve noted the difference between direct sourcing and dealing through intermediaries. Many industry stories reach us of time wasted troubleshooting with parties who neither produce nor understand the molecular nuances at stake. As manufacturers, we benefit from the ability to make real-time adjustments based on lived-through challenges rather than supplied talking points. This includes everything from process optimization to packaging solutions.

    We’ve also discovered that open information sharing delivers better end-user outcomes. Requests for customized grades or application-specific modifications—such as control of particle size, or more secure packaging to reduce volatility—reach resolution in hours rather than weeks. This flexibility comes from our ingrained knowledge of both product chemistry and production logistics, not from relying on generic sourcing sheets or third-party promises.

    Summary of Core Principles Behind Every Batch

    Our long-term partners count on our understanding of every practical and technical dimension behind 1-Benzylpyrrolidin-3-Yl-Methanol. Their projects, from early-stage discovery through to late-phase scaling, often stand or fall on subtle factors: product stability, precise purity, reliable shipment, and responsive technical support. Each improvement we have made stems from hard, practical lessons—missed deadlines, client feedback, costly discard batches—all of which have been addressed through continuous teamwork and technical scrutiny.

    By grounding our production philosophy in direct experience and ongoing feedback, we’ve reached a level of reliability and transparency unmatched by most chemical manufacturers. Whether for novel synthesis in a pharmaceutical startup or for incremental improvement in a global R&D group, 1-Benzylpyrrolidin-3-Yl-Methanol remains a specialty chemical whose manufacture benefits overwhelmingly from real manufacturer insight and adaptation. We remain committed to supporting clients not only as suppliers but as working partners, ensuring every batch reflects not just chemical identity, but decades of lived-through reliability and performance.