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2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride

    • Product Name 2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride
    • Alias N-Methyl-2-chloroethylpyrrolidine hydrochloride
    • Einecs 662-046-0
    • 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

    101245

    Product Name 2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride
    Molecular Formula C7H15Cl2N
    Molecular Weight 184.11 g/mol
    Appearance White to off-white crystalline powder
    Solubility Soluble in water
    Purity Typically ≥98% (may vary by supplier)
    Storage Conditions Store in a cool, dry place; keep tightly closed
    Synonyms N-Methyl-2-(2-Chloroethyl)pyrrolidine hydrochloride
    Chemical Structure Pyrrolidine ring with an N-methyl and 2-chloroethyl substituents, hydrochloride salt
    Hazard Statements May cause skin and eye irritation

    As an accredited 2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Amber glass bottle labeled "2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride, 25g," tightly sealed, with hazard and handling instructions.
    Shipping **Shipping Description:** 2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride is shipped in tightly sealed, chemically resistant containers to prevent moisture and contamination. The package is clearly labeled, handled as a hazardous material, and transported according to regulatory guidelines. Ambient temperature is maintained, avoiding exposure to heat and sunlight during transit for safety and stability.
    Storage 2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride should be stored tightly sealed in a cool, dry, and well-ventilated area, away from light and incompatible materials such as strong oxidizers. Keep the container clearly labeled and avoid exposure to moisture. For safety, store in a chemical cabinet suitable for hazardous or corrosive chemicals, and ensure access is limited to trained personnel only.
    Application of 2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride

    Applications of 2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride in Industrial Manufacturing

    As a dedicated manufacturer, we supply 2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride for recognized industrial applications where this intermediate delivers substantial value in downstream processes. Below, we detail key use cases according to compliance standards, industrial integration, and distinct market outputs, driven by global industry experience and formulation best practices.

    1. Advanced Pharmaceutical Intermediate Synthesis

    This material serves as a critical building block in the production of active pharmaceutical ingredients, particularly in the synthesis of complex alkylating agents and nitrogen-based heterocycles used for oncology and neurology medications. It supports the functionalization of API molecular scaffolds through nucleophilic substitution, demonstrating high selectivity during batch and continuous processes. Formulation chemists adjust active loadings based on reaction scale and structure-activity targets in the route of synthesis, with purity and traceability governed throughout the workflow.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • US FDA 21 CFR Part 211 (Drug Product Quality System)
    • European Pharmacopoeia monographs for API intermediates
    • China NMPA Pharmaceutical Raw Material Registration Guidelines

    Typical usage ratio

    • 0.2–0.8 molar equivalents per target API intermediate, adjusted to minimize excess and maximize conversion according to molecular requirements and reaction pathway optimization studies

    Downstream process integration

    • Charged to alkylation or amination reaction vessels post-initial substrate charging and solvent adjustment; monitored via in-process HPLC or GC analysis for endpoint determination

    Final product types

    • Alkylating API intermediates for anticancer drugs
    • N-heterocycle pharmaceutical intermediates
    • Precursor building blocks for custom synthesis pipelines
    • Reference standards for pharmaceutical QC laboratories

    2. Polymer Crosslinking Agent Precursor

    R&D and specialty polymer manufacturers use this compound as a precursor to functional polymers where controlled crosslinking or grafting of side chains is required. The chlorinated ethyl group undergoes further derivatization to introduce reactive moieties, which then participate in covalent crosslink formation during curing or extrusion. Production teams selectively dose it for property tuning, considering solubility and initiation system when integrating into bulk or solution polymerization streams.

    Industry compliance standards

    • REACH Regulation (EC 1907/2006) for polymer monomers and intermediates
    • ISO 9001:2015 Quality Management for chemical production
    • Polymer-specific standards such as ASTM D1638 for urethanes, depending on application

    Typical usage ratio

    • 0.5–3.0 wt% relative to total monomer or prepolymer feed, with laboratory validation based on mechanical property targets and compatibility with initiators

    Downstream process integration

    • Added to prepolymer or main reactor pre-mix before polymerization; dosing controlled by inline viscosity or monomer conversion measurement

    Final product types

    • Thermoset resin systems for adhesives
    • Functionalized polyurethane foams
    • Specialty elastomers with enhanced chemical resistance
    • Coating additives conferring crosslinked network structures

    3. Agrochemical Intermediate Synthesis

    Crop protection chemical manufacturers employ this compound as an intermediate in the production of specific herbicide and fungicide actives containing substituted pyrrolidine or alkylamino structures. Precision in batch charging and control of reaction temperature are crucial to achieving desired selectivity and minimizing side products that can impact final formulation safety and performance testing in field applications.

    Industry compliance standards

    • FAO/WHO specifications for pesticide technical materials
    • ISO 9001 for consistent agrochemical manufacturing
    • Globally Harmonized System (GHS) for labeling and SDS
    • EC Regulation 1107/2009 for plant protection products (Europe)

    Typical usage ratio

    • 0.3–0.7 molar equivalents per active ingredient precursor, optimized for the synthetic route and impurity control strategy

    Downstream process integration

    • Dosed during the nucleophilic substitution or alkylation stage, frequently under inert atmosphere, with progress monitored via thin-layer chromatography and titration endpoints

    Final product types

    • Pyrrolidine-containing herbicide actives
    • N-alkylated fungicidal compounds
    • Stabilized pesticide intermediates for granule or EC formulation downstream

    4. Specialty Chemical Intermediate for Surfactant Manufacturing

    Specialty surfactant producers integrate this compound into synthesis of cationic surfactants and antistatic agents tailored for use in paints, coatings, textile treatments, and plastics compounding. Its unique nitrogen and chloroethyl substitution enables efficient quaternization, resulting in molecules with improved interfacial properties for demanding industrial and consumer environments. Process engineers tune dosing per desired hydrophilic-lipophilic balance and electrostatic performance, guided by application trial feedback.

    Industry compliance standards

    • ISO 22716 (Cosmetic GMP for surfactant intermediates where relevant)
    • REACH SVHC compliance for surfactant substances
    • Textile Auxiliary Chemicals Eco-Label Standards (e.g., OEKO-TEX 100, ZDHC MRSL)
    • US EPA TSCA regulations for new chemical notification

    Typical usage ratio

    • 1.5–4.0 wt% of reactant loading at the intermediate synthesis stage; precise quantity determined by final surfactant chain length and quaternary group demand

    Downstream process integration

    • Introduced during the amination or quaternization step in batch reactors, usually following seed base addition and before neutralization; tight temperature control ensures consistent product functionality

    Final product types

    • Cationic surfactants for textile softeners
    • Antistatic additives for plastics compounding
    • Dispersants for water-based paints and inks
    • Surface treatment aids for electroplating or paper industries
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