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C-(1-Benzyl-Pyrrolidin-3-Yl)-Methylamine

    • Product Name C-(1-Benzyl-Pyrrolidin-3-Yl)-Methylamine
    • Alias Desmethylprodine
    • Einecs 859-028-6
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    294662

    Chemical Name C-(1-Benzyl-Pyrrolidin-3-Yl)-Methylamine
    Molecular Formula C13H18N2
    Molecular Weight 202.30 g/mol
    Appearance Colorless to pale yellow liquid
    Purity Typically >98% (dependent on supplier)
    Solubility Soluble in organic solvents such as methanol and ethanol
    Density Approx. 1.0 g/cm³ (estimated)
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing Opaque amber glass bottle containing 25 grams of C-(1-Benzyl-Pyrrolidin-3-Yl)-Methylamine, sealed with tamper-evident cap and labeled clearly.
    Shipping Shipping of **C-(1-Benzyl-Pyrrolidin-3-Yl)-Methylamine** is conducted in accordance with chemical safety regulations. The compound is securely packaged in sealed containers, clearly labeled, and shipped via certified couriers. All appropriate handling, documentation, and temperature controls are maintained to ensure compliance and the safe delivery of the product.
    Storage C-(1-Benzyl-Pyrrolidin-3-Yl)-Methylamine should be stored in a tightly sealed container, away from light, moisture, and incompatible substances. Keep it in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Clearly label the container and restrict access to trained personnel. Follow all relevant safety guidelines, including those for handling hazardous organic amines.
    Application of C-(1-Benzyl-Pyrrolidin-3-Yl)-Methylamine

    Applications of C-(1-Benzyl-Pyrrolidin-3-Yl)-Methylamine in Industrial Manufacturing

    As a direct manufacturer, we supply C-(1-Benzyl-Pyrrolidin-3-Yl)-Methylamine to industries that require high-performance intermediates for advanced synthetic processes. Our product integrates into several established industrial value chains, serving as a key building block in pharmaceutical, agrochemical, specialty chemical, and fine chemical production. Below, we detail main application scenarios based on actual customer utilization and regulatory practices.

    1. Active Pharmaceutical Ingredient (API) Intermediate for Central Nervous System (CNS) Drugs

    Major pharmaceutical companies select our raw material as a core scaffold in the synthesis of CNS-active APIs, notably in the production of novel modulators and inhibitors. Manufacturers incorporate this amine early in multi-step syntheses to introduce a functionalized pyrrolidine motif essential for bioactivity. Downstream processors manage stringent documentation, process validation, and batch traceability to meet global market submissions.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) for Active Pharmaceutical Ingredients
    • United States Pharmacopeia (USP) monographs for intermediates
    • European Pharmacopoeia (Ph. Eur.)
    • China Pharmacopoeia (ChP)

    Typical usage ratio

    • 5–15 mol% relative to final API batch, adjusted according to final step yield targets and regulatory requirements for residual intermediates

    Downstream process integration

    • Introduced during early or mid-stage reductive amination or alkylation steps following the construction of core rings; purity often maintained above 98% (HPLC) as per pharmaceutical protocols

    Final product types

    • Central nervous system stimulant or depressant APIs for regulatory-approved drugs
    • Small molecule modulation therapies for neurodegenerative disease pipelines
    • Research-grade CNS active compounds for clinical and pre-clinical trials
    • Reference standards for pharmaceutical quality control laboratories

    2. Key Intermediate for Agrochemical Synthesis

    Companies in crop protection use our material to construct heterocyclic cores in novel insecticides and fungicides, specifically targeting resistance management pipelines. Process engineers optimize the timing and sequence of amine introduction to maximize yield and conform to environmental safety assessments. Quality teams document chain-of-custody, and compliance officers ensure all steps align with market-specific agrochemical standards.

    Industry compliance standards

    • ISO 9001:2015 certified production systems for intermediates
    • Food and Agriculture Organization (FAO) specification for pesticide impurities
    • OECD Test Guidelines for chemical characterization and safety
    • REACH registration (Europe) for industrial intermediates

    Typical usage ratio

    • 3–12 mol% depending on chain propagation mechanism and targeted active ingredient yield; adjusted for regulatory impurity thresholds in each market

    Downstream process integration

    • Added at the stage of heterocyclic ring closure or as a nucleophilic amine during pesticide precursor assembly; process controlled to limit side reactions and residuals below 0.1%

    Final product types

    • Novel fungicides with improved field stability
    • Systemic insecticides for high-value crops
    • Herbicide intermediate stocks for multi-site suppliers
    • Agrochemical testing kits and analytical standards

    3. Intermediate for Specialty Polymer Additives

    Producers of advanced polymers select the amine for the synthesis of custom stabilizers and flame retardant molecules, particularly those engineered to impart performance traits in engineering plastics and elastomers. Production teams specify the integration point for the amine in chain-building sequences and maintain rigorous in-process monitoring to meet customer technical datasheet specifications.

    Industry compliance standards

    • ISO 14001 Environmental Management System
    • European Union Restriction of Hazardous Substances (RoHS) compliance for additives
    • UL 94 flammability standards for polymer compounds
    • ASTM D256 and related ASTM standards for mechanical properties

    Typical usage ratio

    • 1–6 wt% in precursor additive formulations, adjusted according to flame retardancy targets or stabilization requirements for the final polymer

    Downstream process integration

    • Incorporated during additive molecular synthesis, then blended with base polymers via extrusion or reaction injection molding; monitored for compatibility and migration

    Final product types

    • Flame retardant concentrates for use in electrical housings
    • Stabilizing additives for automotive polymer components
    • Specialty polymer masterbatches for appliance applications
    • UV-resistant cable sheath compound additives

    4. Fine Chemical Intermediate for Chiral Building Blocks

    Companies specializing in fine chemical production utilize our raw material to synthesize chiral building blocks for asymmetric catalysis, analytical reference substances, and small molecule research projects. Process engineers target high enantiomeric purity, often requiring customized purification and characterization procedures during batch processing. Laboratory QC checks for each consignment use validated, application-specific analytical methods.

    Industry compliance standards

    • ISO/IEC 17025 accreditation for analytical laboratories
    • Guidelines for Good Laboratory Practices (GLP)
    • Specific purity criteria set in supply agreements with European and North American fine chemical buyers
    • Characterization according to IUPAC nomenclature and reporting standards

    Typical usage ratio

    • Variable—0.5–8 mol% relative to targeted chiral core; actual ratio set by stereochemistry outcome and downstream purification load

    Downstream process integration

    • Employed in enantioselective coupling or reduction reactions following chiral pool or asymmetric catalysis strategy; isolated and characterized via NMR and chiral HPLC

    Final product types

    • Chiral synthons for active compound development
    • Analytical reference standards for stereoisomer testing
    • Enantiomerically pure intermediates for high-value APIs and agrochemicals
    • Research molecules for academic and industrial R&D projects
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