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HS Code |
560551 |
| Chemical Name | 1-Chloro-2,5-dimethoxy-4-nitrobenzene |
| Molecular Formula | C8H8ClNO4 |
| Molecular Weight | 217.61 g/mol |
| Cas Number | 22398-80-7 |
| Appearance | Yellow solid |
| Melting Point | 88-90°C |
| Solubility | Slightly soluble in water, soluble in organic solvents |
| Density | 1.40 g/cm³ (estimated) |
| Smiles | COC1=CC(=C(C=C1Cl)[N+](=O)[O-])OC |
| Inchi | InChI=1S/C8H8ClNO4/c1-13-6-3-8(14-2)7(9)4-5(6)10(11)12/h3-4H,1-2H3 |
| Ec Number | 244-967-2 |
| Synonyms | 2,5-Dimethoxy-4-nitrochlorobenzene |
| Storage Conditions | Store in a cool, dry, well-ventilated place away from light |
As an accredited 1-Chloro-2,5-Dimethoxy-4-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g packaging features an amber glass bottle, tightly sealed, with a white label displaying hazard symbols, chemical name, and handling instructions. |
| Shipping | **Shipping Description for 1-Chloro-2,5-Dimethoxy-4-Nitrobenzene:** Ship this chemical in tightly sealed containers, protected from light and moisture. Follow all relevant hazardous material regulations, as it may be classified as an irritant or environmentally hazardous. Include appropriate labeling, documentation, and safety data sheets (SDS). Avoid exposure to heat, sparks, or open flames during transit. |
| Storage | 1-Chloro-2,5-dimethoxy-4-nitrobenzene should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, heat sources, and incompatible substances such as strong oxidizers or acids. Keep away from moisture and ignition sources. Use secondary containment to prevent spills and clearly label the storage container. |
Applications of 1-Chloro-2,5-Dimethoxy-4-Nitrobenzene in Industrial ManufacturingAs an original manufacturer, we provide 1-Chloro-2,5-Dimethoxy-4-Nitrobenzene to support critical synthesis needs in specialized downstream sectors. The following industrial segments represent genuine, traceable application fields where our product aligns with established industry standards, precise formulation ratios, and rigorous process integration for producing advanced chemical materials. 1. Pharmaceutical Intermediate for API SynthesisThis raw material serves as a key building block in the multi-step synthesis of specific active pharmaceutical ingredients and research compounds. It enters production routes requiring controlled nitration and etherification conditions. Leading manufacturers employ this intermediate in the generation of benzene- or aniline-derived substances where precise molecular substitution is essential for pharmacological profiles. Industry compliance standards
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2. Advanced Dye Intermediate ProductionChemical processing plants use this compound as an aromatic scaffold for synthesizing high-purity azo and nitro dyes. It facilitates regioselective coupling and enhances chromophore development due to its electronic distribution. Manufacturers in the dye sector utilize the material where color fastness and hue precision are critical for technical textiles and specialty inks. Industry compliance standards
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3. Fine Chemical Synthesis for Electronics MaterialsThe electronics sector incorporates this compound in the manufacture of aromatic intermediates essential for synthesizing specialized organic semiconductor materials and liquid crystal components. Its unique halogen and nitro substitution pattern allows for targeted reactivity to obtain strict purity profiles demanded by high-end electronic device production. Industry compliance standards
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4. Agrochemical Synthesis IntermediateAgrochemical active ingredient manufacturers rely on this substance to construct aromatic scaffolds for certain nitro-substituted herbicides and fungicides. The compound’s electron-donating and electron-withdrawing groups support targeted modifications for bioactivity and stability in complex agricultural formulations. Industry compliance standards
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5. Specialty Polymerization Initiators and ModifiersPolymer manufacturers exploit this aromatic structure as a functional modifier or initiator in specialized polymer synthesis. The dual presence of electron-rich methoxy groups and electron-withdrawing nitro and chloro moieties influences initiator reactivity and modifies chain propagation in engineered polymers demanded by high-performance material markets. Industry compliance standards
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