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(1-Benzyl-Piperidin-4-Yl)-Methyl-Amine

    • Product Name (1-Benzyl-Piperidin-4-Yl)-Methyl-Amine
    • Alias 4-Methylaminopiperidine
    • Einecs 684-306-6
    • 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

    642533

    Iupac Name (1-Benzyl-piperidin-4-yl)-methylamine
    Molecular Formula C13H20N2
    Molecular Weight 204.31 g/mol
    Cas Number 934958-85-1
    Appearance White to off-white solid
    Melting Point Unknown
    Boiling Point Unknown
    Solubility Soluble in common organic solvents
    Density Unknown
    Purity Typically >98% (commercial)
    Storage Condition Store at 2-8°C, protected from light
    Canonical Smiles CNCC1CCN(CC1)CC2=CC=CC=C2
    Inchi Key BVGXRGHVNJNMKI-UHFFFAOYSA-N

    As an accredited (1-Benzyl-Piperidin-4-Yl)-Methyl-Amine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White, opaque HDPE bottle containing 50 grams of (1-Benzyl-Piperidin-4-Yl)-Methyl-Amine; features tamper-evident seal and hazard labeling.
    Shipping The shipping of (1-Benzyl-Piperidin-4-Yl)-Methyl-Amine complies with standard chemical transport regulations. The compound is packed in secure, leak-proof containers, labeled appropriately, and shipped by certified carriers. Proper documentation, including safety data sheets and hazard information, accompanies all shipments to ensure safe and compliant delivery. Temperature control is provided if required.
    Storage (1-Benzyl-Piperidin-4-yl)-Methyl-Amine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and direct sunlight. The storage area should be clearly labeled and access restricted to authorized personnel. Keep away from incompatible substances such as strong oxidizers and acids. Follow all relevant chemical safety and regulatory guidelines.
    Application of (1-Benzyl-Piperidin-4-Yl)-Methyl-Amine

    Applications of (1-Benzyl-Piperidin-4-Yl)-Methyl-Amine in Industrial Manufacturing

    As the original manufacturer of (1-Benzyl-Piperidin-4-Yl)-Methyl-Amine, we supply this fine chemical intermediate to select downstream industries where its unique chemical structure and reactivity deliver defined functional outcomes in advanced synthesis environments. Below, we outline how our material supports critical manufacturing segments, grounding each application in specific compliance, technical processing, and product development criteria.

    1. Active Pharmaceutical Ingredient (API) Synthesis for Neurological Treatments

    Downstream pharmaceutical manufacturers incorporate our material primarily as a targeted amination agent during multi-step syntheses of central nervous system (CNS) active pharmaceutical ingredients. Its structure provides reactivity advantages for the creation of substituted piperidine scaffolds, supporting novel drug development projects as well as current generics. Stringent documentation and batch traceability support validation for regulated environments, while formulation chemists adjust input ratios based on the desired API yield and impurity profile according to their process validation data.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • 21 CFR Part 211 (US FDA cGMP for Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.)/USP General Chapters
    • ISO 9001:2015 for Quality Management Systems

    Typical usage ratio

    • 0.5–2.5 molar equivalents per stage, defined by target molecular scaffold and desired synthesis route; actual ratio determined by API synthesis pathway and scale-up balance between purity and throughput

    Downstream process integration

    • Introduced during the amination or reductive amination sequence of multi-step synthesis; reaction monitored by HPLC for conversion toward intermediate or final API molecule

    Final product types

    • Antipsychotic medications
    • CNS stimulant APIs
    • Other monoaminergic therapeutic agents

    2. Fine Chemical Intermediate for Agrochemical Synthesis

    Leading agrochemical compounders utilize this raw material in preparative steps for the synthesis of specific piperidine-derivative insecticides and herbicides. Chemists select its reactive amine site for controlled coupling reactions, enabling the formation of active moieties while maintaining batch homogeneity. Compliance with international agrochemical regulations and internal QMS requirements guides both batch acceptance and traceability for downstream formulation.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • ISO 17025 quality requirements for testing laboratories
    • REACH (Regulation (EC) No 1907/2006) substance registration for agrochemicals
    • China GB/T 28104 quality standards for pesticide intermediates

    Typical usage ratio

    • 0.8–1.2 molar equivalents relative to the coupling reagent or halide substrate; adjusted based on desired conversion rates and minimization of side reactions

    Downstream process integration

    • Added during initial or mid-stage N-alkylation or piperidine ring modification steps; in-process control via GC-MS ensures targeted conversion and elimination of unreacted species

    Final product types

    • Piperidine-based insecticide active ingredients
    • Herbicide intermediates for pre-emergence weed control
    • Compounds for plant growth regulation

    3. Intermediate for Specialty Polymerization Catalysts

    Specialty polymer manufacturers require this compound as a functionalized amine ligand to produce organometallic catalyst complexes used in precision polymerization of engineering plastics. Its molecular configuration effects catalyst geometry, influencing polymer chain tacticity and molecular weight distribution. Handling protocols at customer sites refer to critical control points for impurity prevention, and the ratio of raw material is selected based on the coordination chemistry of the target catalyst.

    Industry compliance standards

    • ISO 9001:2015 for process management
    • Responsible Care® chemical management guidelines
    • EU Regulation (EC) No 1272/2008 on classification, labelling and packaging (CLP)
    • Internal customer-specific catalyst quality protocols

    Typical usage ratio

    • 1.0 molar equivalent per metal center in catalyst synthesis; minor excess (up to 5%) to offset losses during complexation or purification

    Downstream process integration

    • Employed in ligand exchange or direct synthesis step; integrated into anhydrous environment with controlled temperature for catalyst complex formation, followed by purification before deployment in polymerization reactors

    Final product types

    • Organometallic polymerization catalysts (e.g., for polyamide, polyurethane production)
    • Specialty copolymer resins with defined molecular weight
    • High-value engineering plastics with controlled stereochemistry

    4. Building Block for Advanced Fine Chemicals in Electronics

    Manufacturers in the electronics sector draw on this material as a tailored building block in the synthesis of functionalized organic molecules, especially those used in the development of organic light-emitting diode (OLED) emitters and as ligands for complexation in electronic materials. The tight control over structure-activity relationships in end products relies on consistent supply and documented impurity profiles, with integration into synthesis designed for maximum electronic performance.

    Industry compliance standards

    • RoHS Directive (2011/65/EU) on hazardous substances
    • IEC 62474 declarable substances protocol
    • ISO 14001 for environmental management
    • Customer’s electronic material-specific internal QC procedures

    Typical usage ratio

    • 0.2–0.6 molar equivalents in multi-component coupling reactions; adjusted to the electron-donating profile and reactivity demand of target molecules

    Downstream process integration

    • Inserted during key coupling or substitution step for functional group installation on organic backbone; post-reaction purification ensures narrow bandgap properties in resultant materials

    Final product types

    • OLED emitter intermediates
    • Advanced ligands for electronic applications
    • Organic semiconducting materials used in display and sensor components
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