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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 | 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. |
Applications of 2-(2-Chloroethyl)-N-Methyl-Pyrrolidine Hydrochloride in Industrial ManufacturingAs 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 SynthesisThis 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
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2. Polymer Crosslinking Agent PrecursorR&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
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3. Agrochemical Intermediate SynthesisCrop 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
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4. Specialty Chemical Intermediate for Surfactant ManufacturingSpecialty 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
Typical usage ratio
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