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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 | 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. |
Applications of Ethyl 4,5-Bis(2-Methoxyethoxy)-2-Nitrobenzoate in Industrial ManufacturingAs 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 ManufacturingThis 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
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2. UV-Absorber Precursor in High-End Polymer Additive ManufactureIn 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
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3. Photoinitiator Intermediate for Advanced Electronics PackagingWidely 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
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4. Liquid Crystal Intermediate for Display Material FormulationThis 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
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5. Active Ingredient for Advanced Analytical Reagent SynthesisAnalytical 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
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