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2,6-Diethylaniline

    • Product Name 2,6-Diethylaniline
    • Alias 2,6-Diethylbenzenamine
    • Einecs 210-484-7
    • 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
    VTB
    Specifications

    HS Code

    346817

    Cas Number 579-66-6
    Molecular Formula C10H15N
    Molecular Weight 149.23 g/mol
    Appearance Colorless to pale yellow liquid
    Boiling Point 232-233 °C
    Melting Point −30 °C
    Density 0.925 g/cm³
    Refractive Index 1.548
    Flash Point 99 °C
    Solubility In Water Insoluble
    Vapor Pressure 0.03 mmHg (25 °C)
    Synonyms 2,6-Diethylbenzenamine

    As an accredited 2,6-Diethylaniline 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 500 mL of 2,6-Diethylaniline; labeled with chemical name, hazard symbols, and safety handling instructions.
    Shipping 2,6-Diethylaniline should be shipped in tightly sealed containers, labeled according to hazardous material regulations. Transport in a cool, well-ventilated vehicle, away from sources of ignition and incompatible materials. Adhere to local, national, and international shipping guidelines, including documentation and appropriate hazard pictograms. Use secondary containment to prevent leaks or spills.
    Storage 2,6-Diethylaniline should be stored in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Keep it tightly closed in a chemical-resistant container, and protect it from light and moisture. Store separately from oxidizing agents, acids, and strong bases. Proper labeling and secondary containment are recommended to prevent leaks, spills, or accidental contact.
    Application of 2,6-Diethylaniline

    Applications of 2,6-Diethylaniline in Industrial Manufacturing

    2,6-Diethylaniline serves as a key aromatic amine intermediate in a range of specialty chemical supply chains. We ensure controlled manufacturing and stringent QC to support downstream partners in highly regulated sectors. Below, we outline verified applications across established markets, each defined by actual formulation, process, and compliance specifications.

    1. Agrochemical Active Ingredient Synthesis

    This intermediate acts as a building block for several selective herbicides and fungicides, especially in substituted aniline chemistries. Manufacturers rely on its consistent reactivity profile during the synthesis of crop protection agents, as it contributes crucial steric properties required for molecular selectivity. Its presence affects the active moiety formation and biological spectrum in final agrochemical actives.

    Industry compliance standards

    • Regulation (EC) No 1107/2009 for Plant Protection Products—European Union
    • EPA FIFRA Standards—United States
    • ISO 9001:2015 maintained throughout synthesis chain
    • Global GAP for formulators and downstream blenders

    Typical usage ratio

    • Used at 0.1–0.3 molar equivalents relative to target crop protection active, with exact amounts adjusted for conversion yield and impurity profile

    Downstream process integration

    • Introduced following amination or acylation in multi-step batch or continuous reactors
    • Further transformations via alkylation or halogenation, then purified and isolated for formulation

    Final product types

    • Aromatic anilide herbicides (e.g., substituted chloroacetanilides)
    • Substituted benzanilide fungicides
    • Technical grade active ingredients for granular and liquid preparations

    2. Dye & Pigment Intermediate Manufacturing

    Specialty dye makers employ this raw material for synthesizing solvent-soluble and metal-complex colorants, valued for their stability and color saturation in high-performance applications. Its ethyl substitution pattern enables targeted coupling reactions for azo, anthraquinone, and modified phthalocyanine pigment synthesis, contributing to a consistent chromophore structure in the resulting pigment.

    Industry compliance standards

    • REACH Regulation (EC) No 1907/2006—Europe
    • ZDHC Chemical Management for textile applications
    • GMP for Pigments (ISO 9001:2015, additional local standards)

    Typical usage ratio

    • Typical input of 2.5–7 wt% in primary diazotization batches; adjusted based on color strength and batch size

    Downstream process integration

    • Added during diazotization and subsequent coupling in the pigment synthesis train
    • Serves as a co-monomer or modifying amine in closed-system reactors

    Final product types

    • Azo dyes for plastics and synthetic fibers
    • Anthraquinone pigments for automotive coatings
    • Solvent dyes for industrial inks and coloration of lubricants

    3. Pharmaceutical Intermediate Production

    In pharmaceutical intermediate processing, the material acts as a precursor for certain APIs within the antihistamine and local anesthetic families, where ethylated aniline backbones facilitate selectivity and desired pharmacodynamic properties. Strict GMP controls and validated synthesis steps govern its use in regulated manufacturing facilities, especially where trace impurity levels directly impact downstream API safety profiles.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • USP, EP, JP Monograph specifications for intermediates and APIs
    • 21 CFR Part 210/211—FDA CGMP for finished pharmaceuticals

    Typical usage ratio

    • Incoporated at 0.2–0.8 molar equivalents relative to final API, optimised based on stepwise yield and final impurity screening

    Downstream process integration

    • Introduced in early-stage alkylation or amidation reactions within validated synthesis routes
    • Followed by purification via distillation and crystallization before final conversion to API

    Final product types

    • Active pharmaceutical intermediates for antihistamine synthesis
    • Precursors for local anesthetic agents
    • Specialty intermediates for research-grade compounds

    4. Rubber Chemical Synthesis

    Within the rubber processing industry, the compound is utilized as a substituent in the manufacture of antidegradants that prevent oxidative aging in industrial elastomers. Its specific molecular structure contributes to the stabilization mechanism, allowing tire and conveyor belt manufacturers to engineer compounds with superior service lifetimes under high-stress environments.

    Industry compliance standards

    • ISO 9001:2015 for chemical inputs in rubber manufacture
    • ASTM D2000 for elastomer classification
    • EU Regulation (EC) No 1272/2008 (CLP) for additive safety

    Typical usage ratio

    • Usually added at 0.5–2.0 phr (parts per hundred rubber), tailored depending on compound recipe and rubber type

    Downstream process integration

    • Integrated during pre-mixing phase, before compounding with fillers, process oils, and curing agents
    • Acts as an additive in internal mixers and two-roll mill processing

    Final product types

    • Antioxidant-modified tire compounds
    • Rubber conveyor belts with improved service life
    • Technical rubber goods exposed to ozone and oxidizing agents

    5. Specialty Resin and Polymer Additive Production

    This chemical finds use as an intermediary in the synthesis of tailored monomers and resin modifiers for high-heat and chemical-resistant polymers. Its incorporation enhances crosslinking density and imparts select physicochemical characteristics in thermoset and engineering resins, especially where downstream molders demand precise property control for electronics and automotive uses.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in polymerization
    • UL 94 for flammability performance of plastics
    • REACH SVHC screening for specialty additives

    Typical usage ratio

    • Applied at 1.0–4.5 wt% in prepolymer mixtures, varying with targeted crosslink density and thermal property requirements

    Downstream process integration

    • Charged to prepolymerization reactors with base resins and other functional additives
    • Undergoes copolymerization or grafting onto polymer backbones via catalyst-driven mechanisms

    Final product types

    • Chemical-resistant thermoset resins for printed circuit boards
    • High-durability adhesive resins for automotive bonding
    • Custom-engineered composites for aerospace and electronics housings
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