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N-(2-Chloroethyl)Dibenzylamine Hydrochloride

    • Product Name N-(2-Chloroethyl)Dibenzylamine Hydrochloride
    • Alias NSC 15397
    • Einecs 208-088-0
    • 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

    222863

    Product Name N-(2-Chloroethyl)Dibenzylamine Hydrochloride
    Cas Number 910-75-2
    Molecular Formula C16H17Cl2N
    Molecular Weight 294.22 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 174-178°C
    Solubility Soluble in water and ethanol
    Purity Typically ≥98%
    Storage Conditions Store at 2-8°C, tightly closed, dry place
    Synonyms Dibenzyl(2-chloroethyl)amine hydrochloride
    Chemical Structure C6H5CH2N(CH2CH2Cl)CH2C6H5·HCl
    Iupac Name N-(2-chloroethyl)-N,N-dibenzylamine hydrochloride

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

    Packing & Storage
    Packing White, tamper-evident HDPE bottle containing 25 grams of N-(2-Chloroethyl)dibenzylamine hydrochloride, labeled with hazard symbols and lot details.
    Shipping **Shipping Description:** N-(2-Chloroethyl)Dibenzylamine Hydrochloride must be shipped as a hazardous chemical, packaged in tightly sealed, inert containers. It should be transported in compliance with local and international regulations for chemicals, preferably under cool, dry conditions, with appropriate labeling and documentation to ensure safe handling and prevent accidental release.
    Storage N-(2-Chloroethyl)Dibenzylamine Hydrochloride should be stored in a tightly sealed container, away from moisture and direct sunlight, in a cool, dry, and well-ventilated area. Keep it separated from incompatible substances such as strong oxidizers and acids. Store at room temperature, and ensure proper labeling and containment to avoid leaks or contamination. Use appropriate chemical storage cabinets if available.
    Application of N-(2-Chloroethyl)Dibenzylamine Hydrochloride

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

    N-(2-Chloroethyl)Dibenzylamine Hydrochloride plays a critical intermediate role in several high-value chemical manufacturing routes. As a raw material producer, we supply this compound in compliance with relevant sector regulations, targeting specialty downstream applications where its functional group reactivity and purity profile are crucial for customer product line performance.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers use this compound in the targeted synthesis of certain anti-neoplastic and central nervous system active ingredients. Its selective alkylation profile supports stepwise API modification, allowing precise control over reaction yields and impurity profiles. It is crucial to consistently deliver high-purity batches, as minor impurities may trigger OOS events during subsequent QbD and validation steps. Depending on the synthesis route, formulators precisely adjust the addition based on molar ratios necessary for site-specific chemical transformations and downstream process economics.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for APIs
    • European Pharmacopoeia Monographs (as applicable for process route)
    • US FDA 21 CFR Part 211 (where imported to US)
    • Chinese Pharmacopoeia API raw material quality requirements

    Typical usage ratio

    • Reactant charge ranges from 0.9 to 1.2 molar equivalents relative to precursor amines, adjusted based on route selectivity and conversion rates.
    • Pharmaceutical scale batches: typically 1.05–1.1 equivalents to minimize residuals and maximize downstream purity.

    Downstream process integration

    • Material charged in the initial or intermediate alkylation steps, under controlled temperature and solvent systems verified via in-process controls.
    • Real-time monitoring conducted to ensure complete reaction and removal of contaminants before next synthetic step.

    Final product types

    • Cancer therapeutic actives (various custom molecules)
    • Neuropsychiatric API intermediates
    • Specialty pharmaceutical side chains for final API finishing

    2. Synthesis of Specialty Alkylating Agents

    This compound serves as a key building block for downstream manufacturers producing tailored alkylating reagents used in advanced organic synthesis. End users utilize its chloroethyl moiety for site-directed modification of aryl amines and heterocycles, especially where high selectivity and product purity determine end product margin. Reliable upstream supply and consistent batch specification are essential due to sensitivity in downstream process kinetics and finished product quality controls.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006 for chemical intermediates
    • ISO 9001:2015 certified production system
    • TSCA (for shipments to US users)

    Typical usage ratio

    • Added at 1.0 to 1.3 equivalents relative to nucleophile substrate, adjusted according to substrate reactivity and product isolation yield analysis.

    Downstream process integration

    • Fed precisely into batch or continuous flow reactors after substrate charging and solvent preconditioning.
    • Operators tune the feed rate to optimize conversion and limit undesired side product formation, followed by quenching and product extraction.

    Final product types

    • Custom aryl or heterocyclic alkylating agents
    • Advanced intermediates for fine chemical development
    • Reagents for oligonucleotide and peptide modification (research sector)

    3. Polymerization Modifier in Specialty Polymer Production

    Polymer manufacturers employ this compound as a chain-transfer or cross-linking modifier in tailored copolymer systems, particularly where improved chemical resistance or surface functionalization enhances performance properties. The selective introduction of benzyl and chloroethyl groups enables control over polymer network density. Close monitoring of reaction conditions and precise metering maintain batch-to-batch reproducibility, critical for meeting downstream application specs.

    Industry compliance standards

    • ISO 9001:2015 quality management during raw material handling
    • Relevant technical data sheets confirming residual monomer levels
    • Registration under EU Regulation (EC) No 1907/2006 for polymers (where applicable)

    Typical usage ratio

    • 0.5%–2% by weight of total monomer charge, depending on target molecular weight and functional group incorporation goals.

    Downstream process integration

    • Integrated into prepolymerization blends or metered into extrusion reactors post-initiation, followed by in-line viscosity and gel content checks.
    • Polymerization adjustments made in real-time to achieve target mechanical and surface characteristics.

    Final product types

    • High-performance engineering plastics with tailored surface chemistry
    • Coatings for corrosion-resistant applications
    • Specialty elastomer copolymers for industrial sealing and insulating

    4. Advanced Organic Synthesis for Agrochemical Intermediates

    This compound acts as a strategic alkylating intermediate for agrochemical manufacturers developing selective herbicidal or fungicidal ingredients. Its bifunctional structure supports the formation of complex nitrogen-containing scaffolds. Secure and traceable sourcing, as well as demonstrable compliance with environmental and worker safety policies, are essential for downstream regulatory file maintenance and market access in target countries.

    Industry compliance standards

    • ISO 14001:2015 environmental management system
    • Global GAP for upstream raw materials (as required by agrochemical end users)
    • REACH intermediate registration (Europe)
    • Chinese Ministry of Agriculture chemical input registration

    Typical usage ratio

    • Added at 0.8–1.2 molar equivalents in relation to base intermediate, with adjustments according to required scaffold structure and crop-specific regulatory filings.

    Downstream process integration

    • Material charged into initial alkylation stage with specific pH and solvent conditions targeting regioselective formation of active scaffold.
    • Product then isolated, purified, and transitioned to formulation or packaging under local agricultural good manufacturing practices.

    Final product types

    • Agrochemical actives for pre- or post-emergence crop protection
    • Stabilized fungicidal intermediates
    • Herbicidal precursor compounds for export market formulations

    5. Chemical Intermediate for Phase-Transfer Catalyst Manufacture

    Specialty catalyst manufacturers incorporate this compound in the functionalization steps for phase-transfer catalysts, optimizing the balance between hydrophobic and hydrophilic regions. The unique structure enables efficient transfer mechanisms in biphasic reactions used in pharmaceuticals and fine chemicals. Strict analytical control and purity assurance are necessary to avoid catalyst fouling or byproduct formation in sensitive reaction systems.

    Industry compliance standards

    • ISO 17025 laboratory testing for trace impurities
    • ISO 9001:2015 for chemical catalyst component production
    • REACH and K-REACH pre-registration (as relevant for region)

    Typical usage ratio

    • Blended at 1.0 equivalent in the key alkylation or amination step relative to the base quaternary ammonium precursor.

    Downstream process integration

    • Feedstock introduced during quaternization or ammonium salt formation stage; close temperature and mixing control safeguard yield and selectivity.
    • Batch QC sampling ensures required hydrophobic chain distribution in finished catalyst product.

    Final product types

    • Phase-transfer catalysts for liquid-liquid and solid-liquid systems
    • Quaternary ammonium salts with customized alkyl chains
    • Catalysts for pharmaceutical and agrochemical synthesis
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