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Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate

    • Product Name Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate
    • Alias BBMN
    • Einecs 403-720-7
    • 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
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    Specifications

    HS Code

    775178

    Chemical Name Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate
    Molecular Formula C16H21NO8
    Molecular Weight 355.34 g/mol
    Appearance Yellow solid
    Cas Number 1407501-18-3
    Purity Typically ≥98%
    Solubility Soluble in organic solvents such as DMSO and chloroform
    Melting Point Reported ~75-80°C
    Storage Temperature Store at 2-8°C
    Smiles CCOC(=O)C1=C(C=C(C(=C1OC(C)C)OCCOC)OCCOC)[N+](=O)[O-]
    Inchi Key UVKCYMXEYYIISQ-UHFFFAOYSA-N
    Synonyms Ethyl 2-nitro-4,5-bis(2-methoxyethoxy)benzoate
    Application Used as an intermediate in organic synthesis
    Hazard Statements May cause eye, skin, or respiratory irritation

    As an accredited Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate, 25 grams, packaged in an amber glass bottle with tamper-evident seal and clear labeling.
    Shipping Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate is shipped in tightly sealed containers to prevent contamination and moisture ingress. Packages are clearly labeled with chemical identification and hazard information. During transit, it is protected from physical damage, extreme temperatures, and direct sunlight, and handled in compliance with relevant safety and regulatory standards.
    Storage Store **Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate** in a tightly sealed container, placed in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Keep the container clearly labeled and avoid exposure to moisture and heat. Follow all applicable chemical hygiene and safety protocols when handling and storing this compound.
    Application of Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate

    Applications of Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate in Industrial Manufacturing

    As a manufacturer specializing in advanced aromatic esters, we provide Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate for core segments where its chemical profile delivers essential molecular functions. Below are key downstream industries and precise usage scenarios supported by this material, based on prevalent market practice and mature production methods.

    1. Organic Synthesis Key Intermediate for Pharmaceutical API Manufacturing

    This compound serves as an ether-functionalized nitrobenzoate intermediate in select pharmaceutical APIs, especially for stepwise synthesis of complex heterocyclic drugs targeting CNS or anti-infective therapies. Its electron-withdrawing nitro group and solubilizing ethers aid in regioselective reactions during multi-stage syntheses.

    Industry compliance standards

    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • 21 CFR Part 210/211 (US FDA)
    • Ph. Eur., JP Pharmacopoeia monographs for related substances
    • USP General Chapters & Residual Solvent Guidelines

    Typical usage ratio

    • Added at 0.8%–2.5% by weight during condensation or Friedel–Crafts acylation stages; ratio may be varied in accordance with the target molecule and reaction yield optimization.

    Downstream process integration

    • Introduced at the intermediate building block stage, often in controlled reactors under nitrogen, followed by successive catalytic hydrogenations and cyclizations, and then subjected to downstream purification and salt formation steps.

    Final product types

    • CNS-active pharmaceutical ingredients (e.g., substituted benzodiazepines)
    • Antibacterial drug intermediates with enhanced solubility
    • Specialty fine chemicals for medicinal chemistry research

    2. UV-Absorber Precursor in High-End Polymer Additive Manufacture

    In specialty polymer industries, this material acts as a functionalized benzoate precursor to tailor-make UV-absorbers for engineering plastics and high-durability coatings. Substituents enable improved migration resistance and compatibility with polyester and polycarbonate matrices, enhancing long-term colorfastness and weather stability.

    Industry compliance standards

    • ISO 9001:2015 – Quality Management in Chemical Manufacturing
    • REACH Regulation (EC) No 1907/2006 compliance for polymer additives
    • RoHS Directive 2011/65/EU for restricted substances
    • ASTM D5208 (UV Stability Testing Methods)

    Typical usage ratio

    • Generates UV-absorbers dosed at 0.25–1.0 phr (parts per hundred resin) in final polymer blends; ratio adjusted based on polymer matrix UV-resistance targets and additive masterbatch formulation tests.

    Downstream process integration

    • Enters as a core reagent during the synthesis of benzotriazole and oxalanilide-type UV-absorbers, then compounded by extrusion or melt-blending into plastics or coatings as pigment and performance additive.

    Final product types

    • UV-stabilized engineering plastics (e.g., PC, PET, PMMA grades)
    • High-performance automotive coatings
    • Outdoor architectural paints and films

    3. Photoinitiator Intermediate for Advanced Electronics Packaging

    Widely adopted in specialty photoresist and UV-curable resin industries, this compound functions as an intermediate for synthesis of photoinitiators used in advanced electronic packaging, microfabrication, and circuit board solder masks. Its chemical structure allows precise wavelength tuning for selective light absorption, improving definition in micro-patterns.

    Industry compliance standards

    • IEC 61249-2-21 (UL-94, Brominated/Chlorinated Laminates Standards)
    • ISO 14001:2015 Environmental Management Systems
    • JIS C 5016:2017 for Solder Resist Quality in PCBs
    • RoHS 3 (EU 2015/863) for lead-free processes

    Typical usage ratio

    • Formulates at 0.3–2.0% in total photoresist or solder-mask resin batches. The precise loading depends on photo-curing speed, film thickness, and circuit resolution requirements.

    Downstream process integration

    • Applied as a synthonic block in multi-step photoinitiator preparation, then incorporated during blending of photoresist formulations prior to coating, spin-casting, or inkjet application onto substrates.

    Final product types

    • High-resolution printed circuit board solder masks
    • Photolithography resists for semiconductor wafers
    • LED encapsulation resins with tailored UV absorption

    4. Liquid Crystal Intermediate for Display Material Formulation

    This raw material is utilized by specialty liquid crystal producers as a high-purity intermediate to functionalize anisotropic esters, essential for customized nematic phases. Its dual methoxyethoxy groups enhance molecular compatibility and phase behavior control, which is critical in achieving precision electro-optical responses for advanced display panels.

    Industry compliance standards

    • ISO 9001:2015 for Electronic Grade Chemical Production
    • IEC 61290-1 for display component reliability
    • GB/T 30442-2013 for liquid crystal material quality (China)
    • Environmental limits per Sony Green Partner

    Typical usage ratio

    • Typically introduced at 0.5–2.0 mol% relative to total ester components during nematic liquid crystal cocktail formulation, depending on targeted voltage holding ratio and dynamic response specifications required by display manufacturers.

    Downstream process integration

    • Added in controlled-ambient glass reactors during the anisotropic ester synthesis, followed by high-vacuum purification, and blended into proprietary LC formulations prior to panel cell injection.

    Final product types

    • TFT-LCD panel liquid crystal fills
    • OLED panel component mixtures
    • Specialty displays for industrial or automotive instrumentation

    5. Active Ingredient for Advanced Analytical Reagent Synthesis

    Analytical reagent manufacturers employ this compound to develop functional dye and label reagents, owing to its strong chromophore and polar ether functionality which enable stable attachment onto biomolecules or surfaces. These reagents support quantitative detection in pharmaceutical and environmental labs by providing consistent background absorbance for high-sensitivity assays.

    Industry compliance standards

    • ISO/IEC 17025:2017 for laboratory testing and calibration
    • Sigma-Aldrich Analytical Specifications
    • EU REACH (Annex XVII) for reagent-grade chemicals
    • Harmonized Laboratory Chemical Safety Standards (GHS Classification)

    Typical usage ratio

    • Varies between 0.1%–1.5% by weight in diagnostic reagent kits or labeling batches, with concentration calibrated based on the detection method (spectrophotometric or fluorometric) and matrix interference profile.

    Downstream process integration

    • Used as a core dye precursor during diazotization, sulfonation, or coupling steps, then incorporated into finished diagnostic kits, calibration standards, or high-purity chemical labels through filtration and standardized bottling processes.

    Final product types

    • Spectrophotometric reagents for pharmaceutical QC
    • Protein- or DNA-labeling dyes in molecular diagnostics
    • Reference standard kits for environmental analysis
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