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3-Methyl-4-Nitroanisole

    • Product Name 3-Methyl-4-Nitroanisole
    • Alias 3-Methoxy-4-nitrotoluene
    • Einecs 237-697-7
    • 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

    865835

    Cas Number 3282-56-0
    Molecular Formula C8H9NO3
    Molecular Weight 167.16
    Iupac Name 1-Methoxy-3-methyl-4-nitrobenzene
    Appearance Yellow crystalline solid
    Melting Point 37-40 °C
    Boiling Point 282 °C
    Solubility In Water Slightly soluble
    Density 1.22 g/cm3
    Smiles COC1=CC(=C(C=C1)N(=O)=O)C
    Synonyms 3-Methyl-4-nitro-1-methoxybenzene
    Refractive Index 1.582

    As an accredited 3-Methyl-4-Nitroanisole factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Brown glass bottle containing 100 grams of 3-Methyl-4-Nitroanisole, securely sealed, labeled with hazard warnings and product details.
    Shipping 3-Methyl-4-Nitroanisole is shipped in airtight, chemical-resistant containers to prevent leaks and contamination. The packaging complies with international and local regulations for hazardous materials. Proper labeling, cushioning, and temperature control are ensured. Shipping documents include safety data sheets and hazard identification to guarantee safe and compliant transportation.
    Storage 3-Methyl-4-Nitroanisole should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from sources of ignition and incompatible substances such as strong oxidizing agents. Protect from moisture and direct sunlight. Properly label the container and keep it out of reach of unauthorized personnel, following all relevant chemical safety regulations.
    Application of 3-Methyl-4-Nitroanisole

    Applications of 3-Methyl-4-Nitroanisole in Industrial Manufacturing

    As a specialized manufacturer, we supply 3-Methyl-4-Nitroanisole for diverse, validated industrial segments. This intermediate enables precise chemical transformations and controlled product quality in critical downstream syntheses. Below, we outline certified application fields with requirements and integration steps.

    1. Pharmaceutical Intermediate for Active Ingredient Synthesis

    Several API manufacturers employ 3-Methyl-4-Nitroanisole as an intermediate for advanced molecules in antihypertensive and anti-inflammatory drug production. Its methyl and nitro substituents provide selective reactivity for key steps, such as nitration and methylation, supporting multi-stage synthesis routes under GMP conditions. Strict analytical monitoring ensures dimensional consistency and impurity control in each batch throughout campaign production.

    Industry compliance standards

    • GMP (Good Manufacturing Practice, ICH Q7)
    • USP, Ph. Eur., JP monographs for relevant APIs
    • ICH Q3A/B impurity management
    • ISO 9001:2015 Quality Management Systems

    Typical usage ratio

    • Varies from 0.3–1.0 molar equivalents per target molecule
    • Adjusted based on reaction yield and purification recovery
    • Excess of 3-10% permitted to drive completeness of alkylation or nitration
    • Controlled addition rate influences conversion efficiency

    Downstream process integration

    • Introduced in early to mid-stage synthesis as a coupling or nitrating agent
    • Reaction conducted in closed reactors, with continuous monitoring for nitro reduction and methyl displacement
    • Intermediate purification performed via crystallization or solvent extraction
    • Subsequent transformation yields the desired pharmacophore for tabletting or capsule filling

    Final product types

    • Bulk APIs for oral or injectable formulations
    • Semi-finished intermediates for CN-listed pharmaceuticals
    • Active monomers for R&D pilot campaign batches
    • Reference standards for batch release controls

    2. Agrochemical Synthesis for Selective Herbicide Production

    Downstream agrochemical manufacturers use this aromatic nitro compound as a starting block for triazole and substituted aniline herbicides. Its ortho-positioned substituents facilitate specific electrophilic aromatic substitution reactions, scaling in multi-ton batches. The compound contributes to cost-effective process routes and enables consistent halogenation and nitro-reduction profiles across production campaigns, minimizing batch-to-batch deviation.

    Industry compliance standards

    • FAO/WHO technical quality standards for active ingredients
    • ISO 9001 for process documentation
    • ECHA REACH registration and substance tracking
    • EPA (USA) or GB standards for chemical residues and purity

    Typical usage ratio

    • 0.4–0.7 weight fraction as core intermediate stream
    • Usage determined by stoichiometric demand in final active ingredient synthesis
    • Adjusted for crop protection active synthesis input: typically 0.6 kg per 1 kg output
    • Fine-tuned by catalyst efficiency and safety margins

    Downstream process integration

    • Added during initial aromatic ring functionalization step
    • Reacts under controlled temperature with colorimetric endpoint detection
    • Purity stabilized through solvent-phase purification
    • Integrated with grinding and formulation for emulsion concentrates or suspension concentrates

    Final product types

    • Triazole-based selective herbicides
    • Substituted aniline precursor blends
    • Technical concentrates for bulk pesticide manufacturing
    • Plant protection active ingredient masterbatches

    3. Dye and Pigment Intermediate for High-stability Colorants

    Textile and specialty pigment manufacturers utilize 3-Methyl-4-Nitroanisole as a critical intermediate for azo and anthraquinone dye synthesis. Its functional groups allow controlled diazotization and coupling, producing vibrant shades with improved photostability in high-temperature processing applications such as synthetic fibers and plastics. Quality assurance involves batch sampling and spectral purity confirmation to guarantee end-use color specifications.

    Industry compliance standards

    • Oeko-Tex Standard 100 for restricted substances
    • EN 71-3 for pigment safety (toys, plastics)
    • ZDHC MRSL for chemical input management
    • ISO 9001:2015 for colorant quality systems

    Typical usage ratio

    • 5–15% by weight in final pigment synthesis batch
    • Proportion adjusted for desired intensity and absorption spectrum
    • Higher input for deep or blue-shade pigments, lower for pastel grades
    • Residual monitored to ensure compliance with colorfastness requirements

    Downstream process integration

    • Initiated during dye coupling stages, post diazotization of aromatic amines
    • Reacted under low-pH conditions for superior binding to chromophore cores
    • Solid-liquid separation isolates pure pigment crystals
    • Blended into granules or dispersions for application in coatings and masterbatches

    Final product types

    • Azo dyes for polyester and nylon fibers
    • High-stability anthraquinone-based pigments
    • Masterbatch colorants for injection-molded plastics
    • Solvent dyes for industrial paints and inks

    4. Chemical Intermediate for Advanced Electronic Materials

    Manufacturers in the electronic chemical sector incorporate 3-Methyl-4-Nitroanisole in synthesizing specialty monomers and building blocks for dielectric materials and photoresist formulations. Its methoxy and nitro functionalities offer targeted reactivity, supporting functional group conversions critical for polymer backbone modification. The process features high-purity requirements, traceability, and residue analysis to meet electronics industry criteria.

    Industry compliance standards

    • IPC-4101B for laminate and prepreg raw material purity
    • RoHS 3 (EU 2015/863) restrictions for hazardous substances
    • UL 94 for flammability rating of electronic-grade polymers
    • ISO 14001 for environmental systems in electronic material plants

    Typical usage ratio

    • 2–8% by mol in monomer feed for polymer electronics
    • Optimized for dielectric constant and signal transmission requirements
    • Higher purity streams required to limit ionic contaminants
    • Adjusted based on substrate type and feature size in photolithography

    Downstream process integration

    • Fed into reaction columns during monomer functionalization
    • Converted under anhydrous and inert conditions to prevent degradation
    • Purified intermediates polymerized for custom resin systems
    • Pre-assembly testing ensures suitability for wafer and PCB manufacturing

    Final product types

    • Photoresist base chemicals for integrated circuit lithography
    • Polyimide and polyamide-imide dielectric films
    • Conductive polymer precursors for flexible electronics
    • Specialty resins for high-frequency PCB substrates
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