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1-Chloro-2,5-Dimethoxy-4-Nitrobenzene

    • Product Name 1-Chloro-2,5-Dimethoxy-4-Nitrobenzene
    • Alias 2,5-Dimethoxy-4-nitrochlorobenzene
    • Einecs 226-251-1
    • 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

    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 & Storage
    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.
    Application of 1-Chloro-2,5-Dimethoxy-4-Nitrobenzene

    Applications of 1-Chloro-2,5-Dimethoxy-4-Nitrobenzene in Industrial Manufacturing

    As 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 Synthesis

    This 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

    • ICH Q7 Good Manufacturing Practice Guidance for APIs
    • USP-NF monographs (where applicable to intermediates)
    • 21 CFR Part 211 cGMP for finished pharmaceuticals (linked to downstream API use)
    • EU EudraLex Volume 4 for manufacturing controls

    Typical usage ratio

    • Usage varies from 10% to 30% molar ratio depending on stepwise synthesis route.
    • Adjustment based on targeted impurity control and step yield.

    Downstream process integration

    • Introduced during aromatic substitution step before reduction or further modification.
    • Subjected to thorough purification by crystallization or chromatographic separation.
    • Feeds directly into batch reactors for downstream condensation or coupling operations.

    Final product types

    • Intermediate compounds for CNS drugs synthesis
    • Precursors for amine-based pharmaceuticals
    • Custom R&D compounds for clinical predevelopment

    2. Advanced Dye Intermediate Production

    Chemical 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

    • ISO 9001:2015 certified quality management for dye intermediates
    • Oeko-Tex Standard 100 (for non-toxic dyestuffs in textiles)
    • REACH Annex XIV obligations for registration and usage within the EU
    • ZDHC Chemical Management Protocol for zero discharge compliance

    Typical usage ratio

    • Maintained within 5%–15% by weight in the master batch pigment formulation.
    • Ratio fine-tuned for color tone and process throughput.

    Downstream process integration

    • Enters as a primary substrate in the first condensation or diazotization stage.
    • Subjected to controlled heating and pH adjustment for coupling efficiency.
    • Processed in stainless-steel reactors before filtration/purification.

    Final product types

    • High-purity azo dyes for technical textiles
    • Nitro-dye intermediates for specialty solvent-based inks
    • Colorants for industrial plastic compounding

    3. Fine Chemical Synthesis for Electronics Materials

    The 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

    • IEC 62474 for material declaration in electrical and electronic equipment
    • RoHS Directive 2011/65/EU compliance (limiting hazardous substances in electronics)
    • ISO 14001 for environmental management in electronics manufacturing
    • IPC-1752 material declaration requirements

    Typical usage ratio

    • Usage generally ranges from 2% to 7% molar ratio depending on the polymeric matrix or additive route.
    • Final ratio adjusted to meet dielectric property targets or conductivity requirements.

    Downstream process integration

    • Used in the initial monomer synthesis for organic electronics matrices.
    • Integrated in reactor stages with stringent moisture and oxygen controls.
    • Further processed via Suzuki or Heck coupling reactions for polymer chain extension.

    Final product types

    • Organic semiconductors for OLED panels
    • Intermediate molecules for photoresist manufacturing
    • Liquid crystal intermediates for display modules

    4. Agrochemical Synthesis Intermediate

    Agrochemical 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

    • FAO/WHO specifications for agricultural pesticide technical materials
    • ISO 17025 accredited analytical methods for purity/impurity assessment
    • U.S. EPA 40 CFR Part 158 (pesticide product registration and data requirements)
    • REACH registration dossier compliance for agro raw materials in Europe

    Typical usage ratio

    • Typically utilized in concentrations from 8% to 20% by weight in precursor libraries.
    • Adjusted based on required biological activity and stepwise conversion efficiency.

    Downstream process integration

    • Added during the aromatic nitration or halogenation transformation step.
    • Processed with base or acid catalysis under closed-system safeguards.
    • Output used directly for further functionalization into biologically active molecules.

    Final product types

    • Nitroaromatic fungicide intermediates
    • Building blocks for selective post-emergence herbicides
    • Precursors for environmental fate studies

    5. Specialty Polymerization Initiators and Modifiers

    Polymer 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

    • ISO 9001 for quality management in polymer manufacturing facilities
    • ASTM D1186 for polymer coatings and additives (as applicable)
    • FDA 21 CFR 177 for indirect food contact polymers (as relevant to application)
    • ISO/TR 16208 for safety assessment of polymer additives

    Typical usage ratio

    • 0.5%–3% by mass in copolymer or block polymer chain initiation phases.
    • Level set by molecular weight control and desired end-use properties.

    Downstream process integration

    • Dosed at controlled rates in solution or bulk polymerization processes.
    • Enters via continuous feed system for large-batch runs.
    • Blended with co-monomers or chain transfer agents at specific synthesis points.

    Final product types

    • High-durability specialty coatings
    • Modified engineering polymers for automotive or electronics
    • Structurally enhanced polymeric films
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