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N,N'-Dibenzylethylenediamine

    • Product Name N,N'-Dibenzylethylenediamine
    • Alias N,N'-Bis(phenylmethyl)ethane-1,2-diamine
    • Einecs 216-088-1
    • 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
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    Specifications

    HS Code

    995425

    Chemical Name N,N'-Dibenzylethylenediamine
    Molecular Formula C16H20N2
    Molecular Weight 240.34 g/mol
    Cas Number 18868-47-4
    Appearance White to off-white crystalline solid
    Melting Point 93-96°C
    Solubility In Water Slightly soluble
    Density 1.08 g/cm³ (approximate)
    Smiles NCCN(CC1=CC=CC=C1)CC2=CC=CC=C2
    Purity Typically ≥98%
    Storage Temperature Store at 2-8°C
    Synonyms Ethylenediamine, N,N'-dibenzyl-

    As an accredited N,N'-Dibenzylethylenediamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing 250g of N,N'-Dibenzylethylenediamine is supplied in a sealed amber glass bottle with a tamper-evident cap and clear labeling.
    Shipping N,N'-Dibenzylethylenediamine should be shipped in tightly sealed containers, protected from light and moisture. It is typically transported at ambient temperature and labeled appropriately according to chemical regulations. Ensure compliance with relevant safety and transport guidelines (such as DOT, IATA), and include Material Safety Data Sheets (MSDS) with the shipment for safe handling.
    Storage N,N'-Dibenzylethylenediamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Avoid contact with moisture and store at room temperature. Proper labeling and protective measures should be observed to minimize exposure and ensure safe chemical handling.
    Application of N,N'-Dibenzylethylenediamine

    Applications of N,N'-Dibenzylethylenediamine in Industrial Manufacturing

    N,N'-Dibenzylethylenediamine plays a specialized role in several high-value downstream manufacturing sectors, functioning as a critical intermediate or process additive in applications demanding rigorous quality systems and precise formulation controls. The following sections outline established industrial uses with reference to compliance requirements, recommended addition rates, integration into production lines, and finished product categories, based on direct technical experience as a manufacturer.

    1. Active Pharmaceutical Ingredient (API) Synthesis – Chiral Resolution Agent

    Pharmaceutical manufacturers use this compound as a resolving agent for separating racemic mixtures of API intermediates, notably in the production of beta-blockers and related chiral drugs. Selection for this role depends on steric selectivity and salt-forming efficiency, contributing directly to enantiopure substance isolation under high QC scrutiny.

    Industry compliance standards

    • ICH Q7 GMP for API manufacturing
    • USP, EP, JP Monographs (as relevant for each API)
    • FDA cGMP (21 CFR Part 210/211)
    • European Medicines Agency (EMA) quality guidelines

    Typical usage ratio

    • 0.9 – 1.2 molar equivalents per target racemate, adjusted based on stereochemistry and salt solubility screening results

    Downstream process integration

    • Added during the crystallization or salt formation step after intermediate preparation, followed by filtration, washing, and recovery of the resolved chiral intermediate

    Final product types

    • Chiral APIs for cardiovascular, central nervous system, and anti-infective pharmaceuticals
    • Enantiomerically pure pharmaceutical building blocks

    2. Agrochemical Intermediate – Selective Herbicide Component Synthesis

    Manufacturers in the agrochemical sector employ this diamine as an intermediate in multi-step synthesis of selective herbicide actives, especially for forming amide or urea derivatives targeting grass weed control in cereal crops. The ability to introduce benzylic protection in the molecule supports product stability under harsh reaction conditions common in large-scale herbicide plants.

    Industry compliance standards

    • FAO/WHO pesticide specifications
    • ISO 9001 for chemical synthesis
    • REACH registration for chemical intermediates
    • OECD Guidelines for Testing of Chemicals

    Typical usage ratio

    • Stoichiometric proportions; generally 1.0 equivalent per reactive functional group, adjusted for yield optimization during scale-up validation

    Downstream process integration

    • Reacted during condensation, amidation, or coupling steps prior to deprotection and final formulation into technical active ingredient concentrates

    Final product types

    • Active herbicide ingredients for pre- and post-emergent weed control in cereal and oilseed cropping systems

    3. Epoxy Resin Curing Formulation – Latent Hardener in Advanced Composites

    This material acts as a latent hardener component within epoxy resin formulations used by manufacturers of composite materials. Its use in structural adhesives for electronics, automotive assemblies, and aerospace construction allows for controlled heat-activated curing while maintaining storage stability in pre-polymer systems under ambient conditions.

    Industry compliance standards

    • EN 13986 (wood-based panels bonded with thermosetting resins)
    • ISO 9001 (quality management in resin blending and formulation)
    • RoHS Directive for electronic assemblies
    • REACH chemical safety for additives

    Typical usage ratio

    • 2 – 5 wt% relative to resin matrix, with adjustment per glass transition temperature (Tg) and desired open time profiles

    Downstream process integration

    • Blended into epoxy resin base in the pre-polymer mixing phase, with final activation during part molding or assembly by controlled heating cycles (typically 120–150°C)

    Final product types

    • Structural composite panels for automotive lightweighting
    • Electronics-grade encapsulants and laminates
    • Carbon fiber reinforced components for aerospace interiors

    4. Organic Synthesis – Specialty Polymerization Catalyst Precursor

    Chemical synthesis companies utilize this diamine as a catalyst precursor in specialty polymer and oligomer production, particularly for polyurea and polyamide materials used in coatings, adhesives, and fiber applications. Its unique structure favors homogeneous catalyst dispersion, with subsequent processing ensuring stringent end-use performance in engineered polymers.

    Industry compliance standards

    • ISO 14001 for sustainable manufacturing
    • OEKO-TEX Standard 100 (where applicable for textile/dispersant applications)
    • National Chemical Inventory Listings (TSCA, IECSC, etc.)
    • GHS labeling and workplace safety protocols

    Typical usage ratio

    • 0.1 – 0.5 wt% based on total monomer charge, fine-tuned to control polymer chain length and branching in high-volume batch reactors

    Downstream process integration

    • Introduced at the catalyst addition step either as a free base or as a salt, directly preceding the polymerization initiation

    Final product types

    • High-performance polyurea spray coatings
    • Industrial polyamide resins for adhesives and sealants
    • Specialty fibers for filtration media and garment linings
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