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2-(3-Methoxyphenyl)Pyrrolidine

    • Product Name 2-(3-Methoxyphenyl)Pyrrolidine
    • Alias 2-(3-Methoxyphenyl)pyrrolidine
    • Einecs 657-446-9
    • 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

    237993

    Chemical Name 2-(3-Methoxyphenyl)pyrrolidine
    Molecular Formula C11H15NO
    Molecular Weight 177.24
    Cas Number 1370590-39-6
    Iupac Name 2-(3-methoxyphenyl)pyrrolidine
    Appearance Colorless to pale yellow liquid
    Purity Typically >98%
    Solubility Soluble in organic solvents such as DMSO and methanol
    Smiles COc1cccc(c1)C2NCCC2

    As an accredited 2-(3-Methoxyphenyl)Pyrrolidine 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 2-(3-Methoxyphenyl)Pyrrolidine, sealed with a screw cap and labeled with safety data.
    Shipping 2-(3-Methoxyphenyl)Pyrrolidine is shipped in secure, airtight containers to prevent contamination and degradation. The packaging complies with all relevant chemical transport regulations. It is labeled with proper hazard warnings and transported under ambient or controlled temperature conditions, depending on specific requirements, to ensure safe and reliable delivery.
    Storage 2-(3-Methoxyphenyl)Pyrrolidine should be stored in a tightly sealed container, away from direct sunlight, heat, and moisture. Place it in a cool, dry, and well-ventilated area, preferably in a chemical storage cabinet designed for organic compounds. Ensure the storage location is clearly labeled and inaccessible to unauthorized personnel. Follow local regulations and safety guidelines for storage and handling.
    Application of 2-(3-Methoxyphenyl)Pyrrolidine

    Applications of 2-(3-Methoxyphenyl)Pyrrolidine in Industrial Manufacturing

    2-(3-Methoxyphenyl)Pyrrolidine serves as a critical intermediate in specialty chemical manufacturing aimed at pharmaceutical, agrochemical, and advanced material sectors. Our direct production ensures batch traceability for qualified supply chains. Below, we detail the established downstream sectors utilizing our material, each reflecting its specific integration into diverse industrial processes.

    1. Pharmaceutical Intermediate Synthesis for CNS-Active Compounds

    Pharmaceutical companies rely on 2-(3-Methoxyphenyl)Pyrrolidine as a building block for synthesizing advanced nervous system modulators, notably in the pipeline development of analogues targeting dopamine and serotonin pathways. During process development, teams incorporate it as a chiral synthon into multi-step API workflows, typically via nucleophilic substitution or transition-metal-catalyzed coupling to enrich structural diversity. Both early-stage medicinal chemistry and cGMP pilot-plant production need controlled-quality supply to meet escalating batch demands.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Part II
    • 21 CFR Part 211 (US FDA GMP for Finished Pharmaceuticals)
    • Relevant sections of USP, Ph. Eur., JP depending on API registration territory

    Typical usage ratio

    • 5–20% molar input as a structural fragment per API synthesis batch; adjusted according to synthetic route and desired purity.

    Downstream process integration

    • Employed after initial heterocycle synthesis, typically in the stage preceding functional group introduction or side chain alkylation; enters under inert conditions with controlled temperature and stoichiometry to ensure product selectivity and minimize side reactions.

    Final product types

    • CNS-active pharmaceutical ingredients (APIs)
    • Small-molecule drug candidates for clinical trials
    • API intermediates in commercial-scale production

    2. Agrochemical Active Ingredient Development

    Agrochemical formulators integrate 2-(3-Methoxyphenyl)Pyrrolidine during the synthesis of heterocyclic actives with insecticidal or fungicidal action. Its aromatic-methoxy functionalization confers bioactivity advantages when fused onto pyrrolidine-based scaffolds, supporting structure-activity-relationship studies for new crop protection agents. Production teams introduce it in controlled semi-batch reactors, optimizing the ratio for stepwise coupling and ring-forming reactions typical in the development of next-generation plant protection products.

    Industry compliance standards

    • ISO 9001:2015 (Quality Management Systems)
    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO Guidelines for the Registration of Pesticides
    • Relevant local agrochemical registration requirements (e.g., EPA 40 CFR Part 174 in the USA, Regulation (EC) No 1107/2009 in the EU)

    Typical usage ratio

    • 2–8% (w/w) of total precursor input per batch; variable depending on molecular target and yield optimization factors.

    Downstream process integration

    • Added in the coupling or cyclization steps; operators maintain nitrogen or argon atmospheres and tight temperature control to prevent over-oxidation or off-target reactivity during scale-up for field trial quantities.

    Final product types

    • Novel insecticide or fungicide technical concentrates
    • Active ingredient intermediates for downstream formulation
    • Agrochemical actives for regulatory dossier generation

    3. Fine Chemicals for Performance Polymers

    The compound provides a functional monomer or co-monomer backbone in the design of specialty polymers exhibiting increased solubility and controlled-release properties. Polymer scientists dose it precisely during the pre-polymerization feed to modulate physical properties such as flexibility, film-forming, or permeability. Integration is most common in laboratories scaling up research compositions to technical-grade batches that require traceability and compliance with industrial-grade polymer standards.

    Industry compliance standards

    • ISO 9001:2015 (Quality Assurance in Polymer Raw Material Supply)
    • REACH Regulation (EC) No 1907/2006 for Polymer Substances
    • Standard Specification ASTM D883 (Plastics Terminology and Testing)
    • Internal manufacturing QC protocols for specialty performance polymers

    Typical usage ratio

    • 0.5–3% (w/w) in pre-polymer mixtures, depending on desired functional group density and polymer chain length.

    Downstream process integration

    • Incorporated into the monomer feed during solution or suspension polymerization; operators monitor feed rates and reactant purity to secure uniform dispersion and prevent phase separation in the final product.

    Final product types

    • Functional polymers for coatings and adhesives
    • Controlled-release matrix materials
    • Hybrid organic-inorganic composites for industrial coatings

    4. Chiral Auxiliary and Ligand Synthesis for Asymmetric Catalysis

    Research and process-scale manufacturers exploit 2-(3-Methoxyphenyl)Pyrrolidine for the preparation of chiral auxiliaries and ligands used to direct stereoselectivity in asymmetric catalytic reactions. Chemists introduce it as a core moiety in ligand scaffold assembly, leveraging its pyrrolidine framework to promote enantioselectivity in fine chemical and pharmaceutical synthesis, especially in processes requiring highly selective catalytic hydrogenations or cross-couplings.

    Industry compliance standards

    • ISO 17025 (Testing and Calibration Laboratories – for chiral analysis validation)
    • Current Good Manufacturing Practice (cGMP) guidelines for auxiliary material traceability
    • REACH compliance for organometallic reagents
    • Ph. Eur. and USP guidelines when auxiliaries are present in final medicinal APIs

    Typical usage ratio

    • 5–25% molar ratio relative to the substrate; process chemists optimize this according to the targeted enantiomeric excess and catalytic turnover frequency.

    Downstream process integration

    • Charged into reaction vessels during the ligand synthesis or auxiliary installation stage; handlers use inert atmosphere and rigorously dried solvents to avoid racemization or moisture-induced side reactions.

    Final product types

    • Chiral ligands for homogeneous and heterogeneous catalysis
    • Enantiopure intermediates in pharmaceutical synthesis
    • Single-isomer fine chemicals for specialty markets

    5. Research Chemicals for Medicinal Chemistry Screening Libraries

    CROs (Contract Research Organizations) and pharmaceutical research labs source 2-(3-Methoxyphenyl)Pyrrolidine as a fragment in the assembly of screening compounds used in early-stage biological target validation. Its incorporation enables rapid diversification of screening libraries, supporting SAR (Structure-Activity Relationship) mapping in both phenotypic and target-based assays. Material enters the process during parallel synthesis workflows, where rapid derivatization is crucial under controlled aseptic and analytical QC protocols.

    Industry compliance standards

    • OECD GLP principles for laboratory research
    • ISO 9001:2015 for supply chain traceability in research chemicals
    • Material Safety Data Sheet (MSDS) and Reach Annex documentation for lab-scale chemical handling
    • Internal compliance to pharmaceutical client screening compound requirements

    Typical usage ratio

    • 0.2–2% (w/w) per individual parallel synthesis run; flexible depending on library size, molecular uniqueness, and assay throughput demands.

    Downstream process integration

    • Used during the fragment coupling and diversity insertion stages; operators employ small batch reactors with automated liquid handling for accurate dispensation and tracking of material provenance.

    Final product types

    • Medicinal chemistry fragment libraries
    • Screening compounds for high-throughput screening platforms
    • Research intermediates for SAR development
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    Certification & Compliance
    More Introduction

    Meeting Industry Needs with 2-(3-Methoxyphenyl)Pyrrolidine

    The Real-World Benefits Our Clients Value

    We manufacture 2-(3-Methoxyphenyl)Pyrrolidine based on years of experience with fine chemicals and specialty building blocks valued across pharmaceutical and research sectors. Our production line evolved as custom syntheses grew more sophisticated and chemists requested solutions for advanced intermediates. 2-(3-Methoxyphenyl)Pyrrolidine, often known by its short form 3-Methoxyphenylpyrrolidine, stands out in our catalog for a reason. Chemists look for more than purity—they want reliability batch after batch, ease in downstream modification, and full control over stereochemistry when the route demands it.

    The core features in our product trace back to hands-on R&D. We optimize each pilot run internally, adjust conditions to improve yield, and troubleshoot any reproducibility issues on the bench instead of leaving those hidden until scale-up. By providing consistent samples to our application partners, we gather feedback on workability and performance in target syntheses. Our batches commonly reach chemical purity greater than 98%. We have settled on offering 2-(3-Methoxyphenyl)Pyrrolidine most frequently as the racemate. This brings the flexibility necessary for process development and discovery-stage research, where the focus remains on rapid SAR cycles and analog scouting.

    Scalability separates manufacturers from mere traders or distributors. Starting from gram-scale and growing through kilogram and even tonne-scale custom runs, our process control rests on detailed in-house methods. Temperature, solvent residue, and side reactions get traced with HPLC and GC—there is no outsourcing blind spot or lack of control over by-products. We source starting materials from vetted, domestic suppliers and back it up with stability data from actual warehouse samples. The end user sees stability through repeated syntheses, consistent shelf life, and a supply chain built to survive sudden demand or logistics challenges.

    For those in API development, the importance goes beyond just the chemical’s role as a building block. 2-(3-Methoxyphenyl)Pyrrolidine contributes structural motifs for CNS-active molecules and other heterocyclic compounds. Medicinal chemistry teams focus on the methoxy group for its electron-donating effects and pharmacophore fit. We have collaborated on custom modifications, including enantiopure options, when a chiral center turns pharmacologically significant. This is less common in commodity resins—and more common for clients bootstrapping a promising clinical candidate. Our process maintains adaptability when chiral purity must be monitored or if additional deprotection or group exchange paves the way to a new scaffold.

    Clients have pointed out the challenge in finding this compound through standard distributors, especially for scale beyond a few grams. The main bottleneck tends to be inconsistent supply, long lead times from overseas plants, or risk of undisclosed impurity profiles. As a chemical manufacturer, we integrate quality testing directly with shipping logistics, which means large labs and manufacturers avoid frustrating holdups. Regulatory traceability and batch record retention feed into audits or technical transfer projects, supporting each step of a project from request to regulatory filing.

    Specifications Our Team Delivers—Built for Working Chemists

    Product usability grows out of in-house trial and error. We routinely consult with synthetic chemists who request not just the molecule but a sample that dissolves easily, stores safely, and weighs with precision. 2-(3-Methoxyphenyl)Pyrrolidine often comes as a colorless to pale yellow liquid or oil at standard laboratory conditions. Boiling point, density, and solidification profile matter for those running column purifications or intending to derivatize the pyrrolidine ring. Our technical and logistics teams validate each lot against control standards by NMR, HPLC, and mass spectrometry—test results reflect a genuine understanding of the compound’s behavior over time and not simply a basic pass/fail metric.

    We provide clients background on handling conditions, typical storage temperature, and recommend inert atmosphere where reactive cargoes are involved. Peroxide formation and moisture reactivity rarely present a problem in our standard packaging. We also document any solubility limitations when supporting large-scale or process-chemistry projects, reducing the long-term risk of failed reactions or unanticipated losses. Our product labeling and documentation practices follow evidence from decades of shipping to leading pharmaceutical and biotech labs.

    Where 2-(3-Methoxyphenyl)Pyrrolidine Fits—Making a Mark in Medicinal Chemistry

    Choosing the right variant of pyrrolidine-based reagents often makes the difference between a mediocre and an outstanding synthesis. We know from customer feedback and collaborative research that this compound fills a gap not fully addressed by its close relatives. The methoxyphenyl substitution delivers clear reactivity patterns that differ from unsubstituted or alkyl-substituted pyrrolidines, both in coupling efficiency and downstream transformations. Our chemists have overseen dozens of application studies—some clients use it directly as an amine building block, while others prefer to elaborate the aromatic ring or insert chiral auxiliaries at later steps.

    The methoxy group's influence on electronic structure changes the way the molecule reacts in classical Mannich reactions or in metal-catalyzed cross-couplings. We see researchers use 2-(3-Methoxyphenyl)Pyrrolidine as a template for ligand design, particularly where selectivity and electronic tuning are desired. Feedback confirms higher yields or cleaner reaction profiles compared to starting from plain pyrrolidine or alternative aryl-pyrrolidines. Where methyl, ethyl, or halogen substitutions may steer selectivity but suffer in some catalysis environments, the methoxyphenyl group provides a more subtle and tunable modulator.

    Even minor differences stand out under scrutiny. Pure 2-phenylpyrrolidine performs as a straightforward amine donor, but can present unwanted side-reactions or lower selectivity when compared directly to the 3-methoxy derivative. A team in a mid-sized pharmaceutical lab recently reported smoother N-arylation and improved tolerance of acidic or oxidative quench steps. We supply both products on request and openly discuss route comparisons. These hands-on trials give us a practical view into workflow optimization and problem-solving, rather than a superficial claim of superiority.

    From Laboratory to Production—Challenges and Solutions

    Manufacturing intermediates always brings technical and logistical challenges. Customers trust our house-tested workflows when they move past research scale. Our synthetic method relies on batch processing, so we avoid cross-contamination and batch variability endemic to continuous-fed large plants. We employ full lot validation, compliance tracking, and revalidation with each campaign.

    One persistent issue comes from scale-up bottlenecks. Initial favorable yields in the flask can slip as volumes rise. We assign chemists to pilot runs, who document solvent optimization and work-up changes in real time, learning how this compound interacts with diverse glassware, solvents, and process settings. By scheduling validated test runs before major increase in output, our team spots issues—such as color change, unexpected aroma, or phase separation—long before they reach the client’s warehouse. On-the-ground technical support answers questions and supports process handover for toll synthesis or in-house implementation.

    We discovered early on that many buyers encountered difficulties with trace amine or nitrosamine contamination from poorly maintained distributor stocks. Some laboratories stopped projects because of regulatory compliance risks from raw materials. Our team proactively provides impurity data and stress tests, and we share representative analytical tracings on request. This hands-on service grew not from abstract policy, but direct conversations with research heads who insisted on long-term reliability, both chemically and on paper.

    Proven Success Stories and Real-World Feedback

    The journey from early R&D to market-ready asset often hinges not on the central scaffold, but the right building blocks available at the moment of need. Our record tracks partnerships with biotechs that went from five grams to multi-kilogram scale, solving hurdles of shelf stability and batch reproducibility that torpedoed many preliminary runs. We also address concerns around global supply; by maintaining domestic stocks and a quick-turn synthesis window, we refill orders rapidly even when global supply chains fail.

    Pharma partners working with CNS scaffold libraries have reported successful construction of analog sets based on our validated supply of 2-(3-Methoxyphenyl)Pyrrolidine, which allowed preclinical screening to start without interruption. Academic labs often request on-site visits, and we correspond directly with project leaders about minor synthetic dilemmas, last minute specs, and comparative purity concerns. Our ability to provide open analytical data has led to co-authorship in publications and long-term repeat business. Some medicinal chemistry groups added our compound to their internal reference standards, using it to benchmark new reactions and check for long-term method drift.

    The Differences That Matter—Us Versus the Usual Distributor

    There is a clear distinction between what we produce and what typically arrives from commodity distributors. Most traders operate as middlemen—reselling third-party stock, repackaging bulk imports, or shipping long-after storage. That leaves customers vulnerable to delayed supply or omitted batch data. Our end-to-end manufacturing model—one synthesis, one site, traceable from raw precursor to packaged material—provides genuine security and transparency.

    Application support goes hand-in-hand with production. Clients reach out during both troubleshooting and routine method validation. We walk through reaction protocols, examine failed or out-of-range yields, and propose practical adaptations based on prior in-house test results. The collective feedback loop—what works for one partner ends up building the base for the next collaboration. Our records not only reflect HPLC trace or storage log, but the real comments of chemists who ran the reaction last month or corrected the stockroom’s storage temperature.

    The industry's drive toward regulatory compliance only increases the need for trust in supply. Our internal documentation, batch tracking, and transparent COA protocols support teams preparing filings, from DMF to IND. In competitive project environments, early discovery of even a small compositional or handling difference can set one team ahead. We put this knowledge into every order and back it with immediate human support.

    Supporting Future Growth—Forward-Looking Developments

    As medicinal chemistry moves toward higher-throughput screening and more modular synthesis, the demand for unique and reliable intermediates grows. Only manufacturers with a robust technical background and commitment to iterative improvement can keep up. We have invested in automation for both synthesis and purification, integrating real-time process monitoring. This enables rapid response to custom requests and new variations on the 2-(3-Methoxyphenyl)Pyrrolidine backbone.

    Our customized support for chiral resolution, tailored batch size, and downstream application notes builds on our long-standing partnerships with industry leaders. Teams at emerging biotech companies, academic research groups, and global generics producers trust the technical insight behind every batch. As we continue collaborating on new synthetic targets and complex analog synthesis, we refine our protocols based on real outcome data and shared project memories with our customers. Each batch reflects the accumulation of over a decade’s informed decision-making, vendor vetting, and laboratory trial outcomes.

    Choosing Reliability Over Uncertainty

    From our experience, setbacks in project timelines rarely stem from lack of motivation or funding. Bottlenecks emerge from supply gaps, unannounced impurity surprises, or absence of technical support. These are the obstacles we have spent years solving. Our support infrastructure, cross-validated analytics, and openly shared synthetic insights allow project teams to move from hypothesis to pilot and, eventually, from pilot to manufacturing.

    Every lot of 2-(3-Methoxyphenyl)Pyrrolidine leaving our facility carries more than a certificate of analysis—it represents daily work in synthesis, real-time troubleshooting, and hands-on knowledge of what keeps drug discovery moving. For every gram we ship, there is an actual chemist ready to answer a question, share unpublished details from a tricky run, or check a spectral line that matters to your method. That is the real value we bring as manufacturers, not resellers or copywriters. Our focus stays on supporting people and processes behind every successful synthesis.