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1,4-Dimethoxy-2-Nitrobenzene

    • Product Name 1,4-Dimethoxy-2-Nitrobenzene
    • Alias Veratrole-3-nitro
    • Einecs 220-975-9
    • 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

    135448

    Chemical Name 1,4-Dimethoxy-2-Nitrobenzene
    Molecular Formula C8H9NO4
    Molar Mass 183.16 g/mol
    Cas Number 13325-13-8
    Appearance Yellow crystalline solid
    Melting Point 81-83 °C
    Solubility In Water Slightly soluble
    Density 1.29 g/cm3
    Smiles COC1=CC=C(C=C1[N+](=O)[O-])OC
    Pubchem Cid 26272
    Synonyms 2-Nitro-1,4-dimethoxybenzene
    Hazard Statements May cause respiratory irritation

    As an accredited 1,4-Dimethoxy-2-Nitrobenzene factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing A 25g amber glass bottle with tamper-evident seal, labeled "1,4-Dimethoxy-2-Nitrobenzene," featuring hazard symbols and handling instructions.
    Shipping 1,4-Dimethoxy-2-Nitrobenzene is shipped in tightly sealed containers, protected from moisture and direct sunlight. The package is labeled according to hazardous material guidelines, indicating it is an organic nitro compound. Handling and transport comply with local, national, and international regulations to ensure safety during shipping and storage.
    Storage 1,4-Dimethoxy-2-nitrobenzene should be stored in a tightly sealed container, away from light, moisture, and incompatible substances such as strong oxidizers and acids. Keep it in a cool, dry, and well-ventilated area, preferably in a designated chemical storage cabinet. Clearly label the container and follow all relevant safety protocols when handling and storing the compound.
    Application of 1,4-Dimethoxy-2-Nitrobenzene

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

    1,4-Dimethoxy-2-nitrobenzene serves as a key intermediate in multiple specialized chemical industries. Its selective reactivity, purity requirements, and integration into downstream synthesis drive its use in advanced production chains. Below, we outline the principal application scenarios, providing detailed technical context for each sector's standards, formulation ratios, incorporation points, and manufactured products.

    1. Advanced Pharmaceutical Intermediate Synthesis

    As an aromatic nitro compound, 1,4-dimethoxy-2-nitrobenzene is integrated into the manufacture of complex active pharmaceutical ingredients—especially those requiring regioselectively substituted benzene derivatives. Multistep synthesis routes rely on its controlled reactivity during condensation or reduction phases, often directly impacting the pharmacological profile of target APIs. Pharmaceutical production depends on consistency in purity and analytical traceability to meet regulatory standards.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • Local pharmacopeias (e.g., USP, EP) specification for intermediates
    • FDA 21 CFR Part 210/211 for process validation and impurity control
    • ISO 9001:2015 for documentation and traceability

    Typical usage ratio

    • 0.3%–0.7% (w/w) of total synthesis batch, with adjustments based on target molecule yield and excess consumption needed for full conversion

    Downstream process integration

    • Added during the early or mid-stage of multi-step API synthesis—typically after initial aromatic formation and before nitro reduction or nucleophilic aromatic substitution steps

    Final product types

    • Anti-infective drug precursors
    • Analgesic intermediate compounds
    • Specialty anti-cancer molecule precursors

    2. Agrochemical Synthesis—Selective Herbicide Manufacturing

    1,4-Dimethoxy-2-nitrobenzene functions as a pivotal building block in agrochemical sector syntheses for selective herbicide compounds. Its compatibility with nitration and methoxylation chemistry enables precision engineering of molecules that target crop-specific enzymatic pathways. Manufacturers focus on regulatory compliance at every stage, including documented batch traceability and residue analysis.

    Industry compliance standards

    • FAO/WHO Specification for Pesticides (FAO Manual)
    • EPA registration guidelines for new active ingredients
    • REACH (EC) No 1907/2006 for restricted substances
    • ISO 17025 for analytical testing support

    Typical usage ratio

    • 0.2%–0.6% of total formulation, typically optimized per synthetic yield analysis and required excess to achieve target purity in the final product

    Downstream process integration

    • Introduced during the aromatic substitution sequence in herbicide molecule construction, particularly at the step forming key nitro-aromatic intermediates

    Final product types

    • Selective post-emergent herbicides
    • Pre-emergent weed control agents for major grains

    3. Dye and Pigment Intermediate Manufacturing

    In organic colorant industries, 1,4-dimethoxy-2-nitrobenzene fills a specialized niche for the production of nitro-containing azo and anthraquinone dyes. Its substitution pattern allows for selective coupling and oxidative transformations to produce pigments with defined hue and lightfastness parameters. The molecule’s impurity profile and batch consistency are crucial for achieving reproducible coloration and safety in textile and plastics applications.

    Industry compliance standards

    • OEKO-TEX Standard 100 for harmful substance control
    • EU REACH Annex XVII compliance for aromatic amines
    • DIN EN ISO 105 (color fastness testing standards)
    • ZDHC MRSL (Manufacturing Restricted Substances List) for textile dyes

    Typical usage ratio

    • 0.5%–1.5% in batch pigment or dye synthesis, with final ratio defined by target dye shade depth and coupling efficiency

    Downstream process integration

    • Added in the coupling phase of nitro-aromatic dye synthesis, following diazotization or before oxidative ring closure in multi-step pigment production

    Final product types

    • Azo textile dyes for synthetic fibers
    • Cationic dyes for acrylics and polyesters
    • Anionic pigments for inks and high-performance plastics

    4. Specialty Electronic Chemical Manufacturing—Functional Aromatic Compounds

    Electronics manufacturers use 1,4-dimethoxy-2-nitrobenzene as a functional precursor in synthesizing substituted benzene derivatives for organic semiconductors and dielectric materials. Its orthogonal reactivity supports the design of high-purity intermediates that influence current leakage and dielectric loss properties in advanced component production. Full traceability is maintained to comply with electronics industry quality management systems.

    Industry compliance standards

    • IECQ HSPM QC 080000 for hazardous substance management
    • RoHS 2011/65/EU compliance (Restriction of Hazardous Substances)
    • ISO 9001:2015 and ISO 14001:2015 for production and environmental management
    • UL 94 Flammability Standard for plastic encapsulants

    Typical usage ratio

    • 0.1%–0.4% in advanced functional chemical synthesis, adjusted based on the required final electronic grade purity and yield optimization calculations

    Downstream process integration

    • Utilized during the aromatic substitution or cross-coupling phase prior to purification and final performance testing for electronic component feedstocks

    Final product types

    • Organic light-emitting diode (OLED) intermediates
    • Dielectric monomer precursors for capacitor films
    • Specialized aromatic conductors for printed circuit board (PCB) resins

    5. Fragrance and Aroma Compound Intermediate Production

    Fragrance compound houses employ 1,4-dimethoxy-2-nitrobenzene for the creation of specialized aromatic intermediates needed in fine aroma formulation. Its controlled reactivity allows for selective conversion in subsequent reduction and acylation steps, enabling the delivery of aldehyde or ether motifs critical for long-lasting fragrance notes. Adherence to both food and cosmetic grade manufacturing protocols is essential for batch approval.

    Industry compliance standards

    • IFRA (International Fragrance Association) Global Standards
    • ISO 9235:2013 for aromatic raw materials
    • EU Regulation (EC) No 1223/2009 on cosmetic products
    • Food Chemicals Codex (for flavor intermediates)

    Typical usage ratio

    • 0.2%–0.8% depending on conversion efficiency and target aroma intensity; ratio adjusted based on GC-MS analysis of residual intermediates

    Downstream process integration

    • Engaged in early reduction and alkylation stages before introduction of final odor-determining functional groups

    Final product types

    • Fine fragrance intermediates
    • Flavor ingredient precursors for food and beverages
    • Scented formulation bases for detergents and personal care
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