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5-Methoxy-2-Nitrobenzaldehyde

    • Product Name 5-Methoxy-2-Nitrobenzaldehyde
    • Alias 5-Methoxy-2-nitrobenzalcohol
    • Einecs 606-217-7
    • Mininmum Order 1 g
    • Factory Site Tengfei Creation Center,55 Jiangjun Avenue, Jiangning District,Nanjing
    • Price Inquiry sales7@sinochem-nanjing.com
    • Manufacturer Sinochem Nanjing Corporation
    • CONTACT NOW
    VTB
    Specifications

    HS Code

    749015

    Iupac Name 5-Methoxy-2-nitrobenzaldehyde
    Cas Number 7496-03-7
    Molecular Formula C8H7NO4
    Molar Mass 181.15 g/mol
    Appearance Yellow solid
    Melting Point 92-96 °C
    Boiling Point No data available
    Density No data available
    Solubility In Water Slightly soluble
    Smiles COC1=CC(=CC=C1[N+](=O)[O-])C=O
    Pubchem Cid 33894
    Flash Point No data available

    As an accredited 5-Methoxy-2-Nitrobenzaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 5-Methoxy-2-Nitrobenzaldehyde, 25g, is sealed in an amber glass bottle with a tamper-evident cap and safety labeling.
    Shipping 5-Methoxy-2-Nitrobenzaldehyde is shipped in tightly sealed containers to prevent moisture and light exposure. The packaging complies with standard chemical safety regulations. During transit, the product is labeled as a hazardous material, accompanied by all necessary documentation. Handle with care and store in a cool, dry place upon arrival.
    Storage 5-Methoxy-2-Nitrobenzaldehyde should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from heat, sparks, and open flames. Protect from light and incompatible substances such as strong oxidizers and acids. Ensure proper labeling and avoid exposure to moisture. Store at room temperature and keep out of reach of unauthorized personnel.
    Application of 5-Methoxy-2-Nitrobenzaldehyde

    Applications of 5-Methoxy-2-Nitrobenzaldehyde in Industrial Manufacturing

    5-Methoxy-2-Nitrobenzaldehyde serves as a specialty intermediate across several advanced manufacturing sectors. As an established upstream chemical produced in-house under strict process controls, it plays a critical role in diverse end-use applications ranging from pharmaceutical synthesis to the development of high-performance dyes. Below, we detail its real-world industrial roles, compliance frameworks, formula recommendations, processing positions, and representative end products.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    This compound acts as a crucial building block in the synthesis of certain active pharmaceutical ingredients, particularly within anti-infective and central nervous system (CNS) therapeutic classes. Medicinal chemistry utilizes its aromatic aldehyde structure for selective condensation and nitration reactions to yield advanced pharmaceutical intermediates. Its reliability and traceability support stringent GMP pharmaceutical manufacturing environments, where controlled reactivity and high purity are essential for final API quality.

    Industry compliance standards

    • ICH Q7 (Good Manufacturing Practice for Active Pharmaceutical Ingredients)
    • EU GMP, Part II: Basic Requirements for Active Substances
    • US FDA 21 CFR Part 211 (Finished Pharmaceuticals)
    • European Pharmacopoeia (Ph. Eur.) requirements for chemical purity

    Typical usage ratio

    • 0.5%–2.5% of total reaction mass in key intermediate stage, averaging 1.8% for CNS actives. The value adjusts with target molecule complexity and desired step yield.

    Downstream process integration

    • Introduced during the initial aromatic aldehyde condensation stage or as a nitration precursor, prior to chain elongation, cyclization, or reduction steps in multi-step synthesis of APIs.

    Final product types

    • Active intermediates for cephalosporin derivatives
    • Precursors for CNS modulators (e.g., anticonvulsants, antipsychotics)
    • Reference standards for method validation

    2. Development of Advanced Azo and Disperse Dyes

    The aromatic nitro and methoxy functionality allow chemical formulators to produce bright, high-fastness dyes used in the textile and plastics industries. Niche azo and disperse dye production utilize this material as a diazo component to enable specific color shade development and enhanced color stability. Direct pigment manufacturers also select this intermediate for formulating dyes with elevated light and wash fastness for technical textiles.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (Textile Chemical Safety)
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • REACH Annex XVII (Restrictions on certain hazardous substances)
    • BASF Global Dye Safety Criteria

    Typical usage ratio

    • 1.2%–3.0% of dye lot formulation. Specific concentration depends on target chromophore group and intended dye depth; higher percentages enable deeper shades in polyester disperse systems.

    Downstream process integration

    • Integrated as an initial diazo or coupling component during the azo bond-forming stage of dye synthesis, before isolation, salt formation, and spray drying of the dye product.

    Final product types

    • High-fastness disperse dyes for polyester fiber
    • Azo dyes for high-performance polyamide (nylon) fabrics
    • Custom shades in specialty plastic masterbatches

    3. Fine Chemical Synthesis for Agrochemical Actives

    This material functions as a precursor in the production of select agrochemical intermediates, particularly where specificity in aromatic substitution supports the synthesis of advanced herbicide or pesticide molecules. It ensures the regioselectivity needed for downstream coupling and controls impurity profiles under regulated agricultural production frameworks. Agrochemical formulators rely on it for consistent batch-to-batch synthesis fidelity.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • US EPA 40 CFR Part 180 (Tolerances and Exemptions for Pesticide Chemicals in Food)
    • ISO 9001:2015 Quality Management (specific to fine chemicals)
    • European Crop Protection Association (ECPA) guidelines

    Typical usage ratio

    • 0.8%–1.5% of the main reaction charge, commonly 1.0% for target herbicide intermediate synthesis. Modulated by scale batch size and impurity management requirements.

    Downstream process integration

    • Charged as an aldehyde component before amide or oxime formation in the agrochemical active ingredient synthesis, followed by purification and formulation into technical concentrate.

    Final product types

    • Agrochemical intermediates for selective herbicides
    • Precursors for systemic insecticides and fungicides
    • API-standard fine chemicals for regulated plant protection agents

    4. Specialty Fragrance and Flavor Chemical Manufacture

    In the fragrance and flavor industry, aromatic aldehyde derivatives provide essential notes or act as intermediates in the creation of complex synthetic aroma compounds. The structural motifs of this compound allow downstream chemists to synthesize molecules used in scent and flavor development, imparting subtle olfactory notes for use in perfumery or as intermediates for vanillin and anisaldehyde analogs. Its consistent purity ensures repeatable chromatographic profiles in critical ingredient authentication protocols.

    Industry compliance standards

    • IFRA (International Fragrance Association) Standards
    • US FDA 21 CFR Part 172 (Food Additives Permitted for Direct Addition to Food)
    • EU Regulation (EC) No 1334/2008 (Flavorings and Certain Food Ingredients with Flavoring Properties)
    • ISO 9235:2013 (Aromatic Natural Raw Materials)

    Typical usage ratio

    • 0.05%–0.2% in compounded base; advanced isolates adjust within this range based on target intensity and compliance with maximum residue thresholds.

    Downstream process integration

    • Reacted in the aldehyde derivatization or etherification stage immediately prior to blending into compounded fragrance bases or downstream extraction of primary aroma molecules.

    Final product types

    • Synthetic intermediates for fine fragrances and perfumes
    • Flavor chemical precursors (e.g., anisic notes, sweet-vanillic bases)
    • Aroma molecules for non-food consumer goods (detergents, air fresheners)
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