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Methyl Piperidine-3-Carboxylate

    • Product Name Methyl Piperidine-3-Carboxylate
    • Alias Methyl 3-piperidinecarboxylate
    • Einecs EINECS 687-731-4
    • 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

    863033

    Cas Number 1122-97-0
    Molecular Formula C7H13NO2
    Molecular Weight 143.18 g/mol
    Iupac Name methyl piperidine-3-carboxylate
    Appearance Colorless to pale yellow liquid
    Boiling Point 79-81°C at 14 mmHg
    Density 1.045 g/mL at 25°C
    Solubility Soluble in organic solvents; slightly soluble in water
    Melting Point -12°C
    Smiles COC(=O)C1CCNCC1
    Inchi InChI=1S/C7H13NO2/c1-10-7(9)6-3-2-4-8-5-6/h6,8H,2-5H2,1H3
    Refractive Index 1.471

    As an accredited Methyl Piperidine-3-Carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Methyl Piperidine-3-Carboxylate, 100g, securely sealed in an amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping Methyl Piperidine-3-Carboxylate should be shipped in tightly sealed containers, stored in a cool, dry place away from incompatible substances. It is classified as a chemical reagent and may require labeling according to hazardous materials regulations. Appropriate documentation and packaging must ensure safety and compliance with local and international shipping standards.
    Storage Methyl Piperidine-3-Carboxylate should be stored in a tightly closed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and direct sunlight. Keep it separate from incompatible substances such as strong oxidizers and acids. Store at room temperature, and ensure proper labeling and access only to trained personnel. Follow relevant chemical safety and storage guidelines.
    Application of Methyl Piperidine-3-Carboxylate

    Applications of Methyl Piperidine-3-Carboxylate in Industrial Manufacturing

    Methyl Piperidine-3-Carboxylate serves as a critical intermediate in several specialized industrial production lines. Its unique chemical structure makes it valuable for fine chemical synthesis, pharmaceuticals, agrochemical development, advanced polymer manufacture, and high-purity laboratory reagents. Below, we detail major downstream applications and integration protocols, focusing on factual industry practice and regulatory frameworks.

    1. Pharmaceutical API Synthesis – Piperidine-Based Drug Precursors

    Our material is extensively used in the synthesis of active pharmaceutical ingredients, particularly those involving piperidine scaffolds for central nervous system therapeutics and antipsychotics. CDMOs and in-house pharma manufacturing teams incorporate it during the early-stage formation of complex heterocyclic molecules. Validated processes utilize this intermediate in multi-step sequences for the creation of compounds such as risperidone and related derivatives. Strict traceability and impurity profiling are required from the point of material reception through to API crystallization, as mandated by regulatory filings.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) reference standards
    • United States Pharmacopeia (USP) monograph guidelines
    • FDA 21 CFR Part 211 (Current Good Manufacturing Practice for Finished Pharmaceuticals)

    Typical usage ratio

    • Typical inclusion at 5–15% molar ratio in piperidine ring assembly steps, based on target molecule scale and desired conversion yields.

    Downstream process integration

    • Material enters as a building block during the condensation or alkylation stages before cyclization and additional functionalization.
    • Used in controlled batch or continuous flow reactors under nitrogen atmosphere to minimize contamination and side-reactions.

    Final product types

    • Finished central nervous system drugs such as risperidone and ziprasidone
    • Piperidine-based oral and injectable API compounds
    • Intermediates for anti-tubercular pharmaceuticals

    2. Agrochemical Intermediate Production – Herbicide and Insecticide Synthesis

    Chemical manufacturers employ our material in the formulation of key agrochemical moieties, especially where nitrogen heterocycles provide enhanced biological activity. It acts as a core intermediate in the stepwise synthesis of selective herbicides and systemic insecticides. Formulation chemists precisely control reaction conditions and purity to meet agrochemical market authorizations, especially for products targeting high regulatory jurisdictions such as the EU and Japan.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH Registration, Evaluation, Authorisation and Restriction of Chemicals (EU)
    • Japan Agricultural Chemicals Regulation Law
    • GLP (Good Laboratory Practice) OECD principles

    Typical usage ratio

    • Usually 3–12% mass basis relative to total synthetic reactant mass, adjusted for desired active ingredient purity, with yields optimized for downstream coupling efficiency.

    Downstream process integration

    • Incorporated in multi-step synthesis following chloroalkylation, participating in cyclization or amidation reactions to finalize heterocyclic pesticide cores.
    • Fed into closed-reaction systems with in-line real-time analytics for purity assurance.

    Final product types

    • Nitrogen-heterocycle herbicides
    • Systemic piperidine-based insecticides
    • Crop protection agent intermediates supplied to formulation plants

    3. Advanced Polymer Modification – Specialty Polyamide and Polyurethane Additives

    Compounders in the performance plastics sector use this material as a reactive intermediate to enhance flexibility, chemical resistance, and surface properties of engineered polyamides and polyurethanes. It integrates into polymer backbones via ring-opening and isocyanate-ester reactions, enabling product differentiation for specialty automotive, electronic, and industrial coatings. Quality teams conduct detailed analysis to monitor residual levels and ensure downstream compliance with product safety laws.

    Industry compliance standards

    • ISO 9001 Quality Management Systems
    • EU Regulation (EC) No 1907/2006 (REACH)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • UL 94 Flammability Standards for Plastics

    Typical usage ratio

    • Integrated at 0.8–3.5% by weight relative to total polymer matrix, based on desired impact on glass transition temperature, flexibility, or chemical functionality.

    Downstream process integration

    • Added during melt compounding or prepolymer formation, with careful thermal management to prevent degradation and preserve target molecular weights.
    • Low-dust charging systems employed to meet occupational exposure limits and control batch homogeneity.

    Final product types

    • Modified engineering-grade polyamides
    • Specialty polyurethanes for automotive interiors
    • Conductive and antistatic plastics for electronics

    4. High-Purity Laboratory Synthesis – Research and Diagnostic Chemical Production

    Producers of specialty research reagents and diagnostics rely on our material for its reliability in multi-step laboratory synthesis, where lot-to-lot reproducibility and documented purity are essential. Analytical and life science companies use it in constructing small-molecule probes, custom reference standards, and specialized molecular tags. Detailed certificates of analysis and impurity profiles are provided for every batch, enabling traceability in critical research applications.

    Industry compliance standards

    • ISO 17025 Laboratory Accreditation
    • Good Laboratory Practice (GLP)
    • National Institute for Standards and Technology (NIST) reference protocols
    • ACS Reagent Grade requirements where applicable

    Typical usage ratio

    • Ranges from 1–25% molar basis, largely determined by the stoichiometric requirements of targeted probe or reagent synthesis and the degree of labeling needed for final application.

    Downstream process integration

    • Introduced during initial synthetic steps for labeled molecule construction or used as a functionalization substrate in tag derivatization protocols.
    • Maintained in atmospherically controlled environments to minimize moisture uptake and impurity ingress.

    Final product types

    • Small-molecule research probes
    • Reference standards for analytical instrument calibration
    • Diagnostic labeling agents for clinical assay kits
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