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3-Hydroxy-1-Methylpiperidine

    • Product Name 3-Hydroxy-1-Methylpiperidine
    • Alias 3-Hydroxy-N-methylpiperidine
    • Einecs 629-541-1
    • 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

    990685

    Cas Number 25509-81-5
    Molecular Formula C6H13NO
    Molecular Weight 115.17 g/mol
    Iupac Name 3-hydroxy-1-methylpiperidine
    Appearance Colorless to pale yellow liquid
    Boiling Point 197-200°C
    Melting Point -7°C
    Density 0.96 g/cm³
    Solubility In Water Miscible
    Purity Typically ≥ 98%
    Refractive Index 1.478
    Flash Point 80°C
    Synonyms 1-Methyl-3-hydroxypiperidine
    Storage Temperature Store at 2-8°C
    Smiles CN1CCC(C1)O

    As an accredited 3-Hydroxy-1-Methylpiperidine 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 100 g of 3-Hydroxy-1-methylpiperidine, tightly sealed with a screw cap and tamper-evident label.
    Shipping 3-Hydroxy-1-Methylpiperidine is shipped in tightly sealed containers, protected from moisture and light. It is usually packed in amber glass bottles or HDPE containers, labeled with hazard information. Transport occurs according to local and international regulations, ensuring safety and preventing leaks or exposure during handling and transit.
    Storage 3-Hydroxy-1-Methylpiperidine should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and acids. Protect it from moisture and direct sunlight. Store at room temperature, and keep away from ignition sources. Clearly label the storage container and ensure proper chemical safety protocols are followed.
    Application of 3-Hydroxy-1-Methylpiperidine

    Applications of 3-Hydroxy-1-Methylpiperidine in Industrial Manufacturing

    As a direct manufacturer of high-purity 3-Hydroxy-1-Methylpiperidine, we support a range of specialized industrial sectors with stringent compliance demands and established downstream processes. Below, we detail verified application scenarios, based on current industry practice and real-world integration.

    1. Pharmaceutical Intermediate for Antiviral and CNS Agents

    Pharmaceutical producers employ 3-Hydroxy-1-Methylpiperidine as a key building block in the synthesis of both antiviral compounds and central nervous system (CNS) pharmaceuticals. The material serves as a vital structural precursor during the assembly of complex piperidine-based scaffolds, undergoing selective functionalization and incorporation in multiple synthetic stages. Finished APIs made using this raw material must conform to international harmonized pharmacopeial standards, demanding consistently high quality and tight control of secondary amines and chiral purity.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice (GMP) Guideline for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) synthesis routes and impurity controls
    • United States Pharmacopeia (USP) general requirements for pharmaceutical intermediates
    • 21 CFR Part 211 - US FDA cGMP for Finished Pharmaceuticals (where relevant)

    Typical usage ratio

    • 0.15–0.7 molar equivalents, relative to primary reactant in the target molecule’s core construction step; practical amounts tailored per API yield and route optimization

    Downstream process integration

    • Introduced during multi-step organic synthesis, frequently in nitrogen-inerted batch reactors at mid-stage or late-stage positions prior to cyclization, reductive amination, or alkylation

    Final product types

    • Finished small-molecule APIs for antiviral therapies
    • Piperidine-derived CNS drug substances, including select antipsychotic and antiepileptic agents

    2. Crop Protection Synthesis—Herbicide and Fungicide Intermediates

    Agrochemical manufacturers use 3-Hydroxy-1-Methylpiperidine as a starting material to construct novel piperidine-based intermediates in the synthesis of advanced herbicides and fungicides. Its reactivity supports regioselective cyclization and protection strategies, which can significantly affect biological activity and selectivity in the final agrochemical products. Specifications must align with regulations concerning pesticide precursor traceability and byproduct content, especially for export-controlled active ingredients.

    Industry compliance standards

    • FAO/WHO Specifications and Evaluations for Agricultural Pesticides
    • REACH (Registration, Evaluation, Authorisation and Restriction of Chemicals) Registration Dossiers for agrochemical intermediates
    • OECD Good Laboratory Practice (GLP) for pre-market screening
    • China GB/T 1604—Technical requirements for pesticide intermediate quality

    Typical usage ratio

    • 2–8% by mass in stepwise addition for intermediate-stage condensation, adjusted based on final molecule’s heterocyclic system and chain length requirements

    Downstream process integration

    • Employed during early-to-intermediate synthesis steps in stirred-tank reactors before final chlorination, methylation, or sulfonation in the active ingredient process

    Final product types

    • Piperidine-derived herbicide actives, such as certain ALS inhibitors
    • Fungicidal active ingredients with piperidine motifs in their core structure

    3. Specialty Polymer Additive—Chain Modification for High-Performance Plastics

    Specialty polymer manufacturers utilize 3-Hydroxy-1-Methylpiperidine as a reactive chain modifier or capping agent to impart improved flexibility, enhanced hydrolysis resistance, and unique surface properties to engineering plastics and coatings. It is particularly valued in the synthesis of high-performance polyamides and functional polyurethanes, where precise molar dosing and impurity control are essential to material consistency and compliance with safety restrictions on nitrosamine precursors and migration.

    Industry compliance standards

    • ISO 9001 Quality Management System for specialty polymers and additives
    • EN ISO 1043-1: Plastics—Symbols and structure code for chemicals in polymers
    • EU Regulation (EC) No 1935/2004 for food contact polymers (where intended use applies)
    • RoHS Directive 2011/65/EU Annex II, restriction of hazardous substances

    Typical usage ratio

    • 0.5–6 parts per hundred resin (phr), depending on desired mechanical enhancement and the chain length of the target polymer

    Downstream process integration

    • Blended or reacted into pre-polymer blends during melt compounding or solution polymerization; can serve as an end-capper introduced right before polycondensation or curing steps

    Final product types

    • High-modulus polyamides for automotive and electrical housings
    • Polyurethane coatings with enhanced abrasion and chemical resistance
    • Speciality copolymers for optical or electronic encapsulation

    4. Fine Chemical Intermediate for Fragrance Ingredient Synthesis

    Producers of aroma chemicals incorporate 3-Hydroxy-1-Methylpiperidine into synthetic routes for advanced piperidine-containing fragrance compounds, which provide unique notes of spiciness or soft musk in high-end perfumery and functional fragrances. The raw material’s specificity is key for regioselective substitutions and cyclizations in cis/trans isomer generation. All precursors in this sector must pass exhaustive purity screening for allergenic amines and conform to international fragrance safety regulations.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards for fragrance ingredient purity
    • ISO 9235: Aromatic natural raw materials and synthetic chemicals for perfumery
    • EU Cosmetics Regulation (EC) No 1223/2009 for fragrance ingredient safety evaluation
    • REACH Annex XVII compliance for restricted chemical components in consumer fragrances

    Typical usage ratio

    • 1–4 mol% of total reactants, calculated relative to target molecule size based on olfactory intensity optimization in the final product

    Downstream process integration

    • Fed into batch reaction stages for graded hydrogenation or acylation; the material allows for efficient cyclization and amine protection prior to distillation or extraction purification

    Final product types

    • Piperidine-based fragrance aldehydes
    • Musk ketones and spirocyclic aroma compounds
    • Specialty perfumery intermediates for fine fragrance blending
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