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2-Methyl-5-Nitroanisole

    • Product Name 2-Methyl-5-Nitroanisole
    • Alias 2-Methoxy-1-methyl-4-nitrobenzene
    • Einecs 243-102-4
    • 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

    834625

    Chemical Name 2-Methyl-5-Nitroanisole
    Cas Number 57849-60-4
    Molecular Formula C8H9NO3
    Molecular Weight 167.16
    Appearance Yellow solid
    Melting Point 64-68°C
    Solubility Slightly soluble in water
    Smiles CC1=CC(=C(C=C1)OC)[N+](=O)[O-]
    Storage Conditions Store in a cool, dry place
    Synonyms 2-Methyl-5-nitro-1-methoxybenzene

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

    Packing & Storage
    Packing The packaging for 2-Methyl-5-Nitroanisole (25g) is a sealed amber glass bottle with a secure screw cap and clear labeling.
    Shipping 2-Methyl-5-Nitroanisole is shipped in tightly sealed containers to prevent leakage and contamination. It is typically transported as a solid at ambient temperature. Proper labeling and documentation are required, and the shipment must comply with relevant regulations for handling chemicals. Store in a cool, dry place away from incompatible materials.
    Storage 2-Methyl-5-Nitroanisole should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and strong oxidizing agents. Protect the chemical from light and moisture. Ensure that appropriate chemical spill containment and fire suppression measures are in place. Properly label the container and restrict access to authorized personnel only.
    Application of 2-Methyl-5-Nitroanisole

    Applications of 2-Methyl-5-Nitroanisole in Industrial Manufacturing

    Our proprietary 2-Methyl-5-Nitroanisole is a specialty intermediate utilized in multiple advanced manufacturing streams, contributing to high-value downstream syntheses for leading chemical sectors worldwide. Below, we detail key applications, specific manufacturing requirements, integration pathways, and associated end products for each principal industry channel.

    1. Pharmaceutical Active Pharmaceutical Ingredient Synthesis

    In pharmaceutical compound manufacturing, this intermediate is essential for building nitro-anisole moieties in selective API synthesis. Multi-step syntheses of antihypertensive, antifungal, and anti-inflammatory ingredients rely on its aromatic reactivity to introduce methoxy nitro groups during condensation or cyclization reactions. Process engineers determine precise charge-in points to maximize conversion yield, following strict process control to ensure ultra-high purity and batch reproducibility for regulated drug manufacturing environments.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guide for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs for related API synthesis
    • US FDA 21 CFR Part 211 for finished pharmaceuticals
    • China Pharmacopoeia (ChP) requirements for intermediates

    Typical usage ratio

    • Applied in a 1.0–1.4 molar equivalent to the corresponding substrate, optimized by stoichiometry studies for target yield and impurity profile control

    Downstream process integration

    • Charged during early-stage condensation or nitration steps prior to heterocycle formation or amidation; enters the reactor with strict temperature and pH controls to prevent decomposition

    Final product types

    • Antihypertensive drugs (e.g., specific substituted benzodiazepines, ARB-class APIs)
    • Antifungal agents requiring anisole-nitro scaffolds
    • Anti-inflammatory APIs utilizing nitroanisole fragments
    • Veterinary pharmaceutical actives derived from aromatic intermediates

    2. Agrochemical Active Ingredient Manufacturing

    The compound acts as an essential building block in the synthesis of select nitroanisole-based pesticide and herbicide actives. Agrochemical formulators employ it in their synthetic routes for producing pre-emergent herbicides and broad-spectrum fungicides where electron-rich, substituted aromatic motifs confer field stability and biological activity. Careful process management ensures minimal byproduct formation and high-throughput performance in continuous or batch production lines.

    Industry compliance standards

    • FAO/WHO Specifications for Plant Protection Products
    • REACH (EC No. 1907/2006) Registration, Evaluation, Authorisation and Restriction of Chemicals
    • US EPA Pesticide Ingredient Reporting
    • ISO 9001:2015 certified management systems in agrochemical plants

    Typical usage ratio

    • Introduced at 2–8% weight of total intermediate mass, depending on required active loading and sidechain modifications in the synthetic route

    Downstream process integration

    • Added during initial aromatic substitution stages or as a core fragment for coupling and subsequent nitration within closed reactors under nitrogen blanket for safety and yield assurance

    Final product types

    • Herbicides for broadleaf and grass weed management in cereal crops
    • Fungicidal actives with persistent environmental profiles
    • Intermediate scaffolds for multi-site pesticide formulations
    • Safener agents used to protect crops against broad-spectrum chemicals

    3. Dyestuff Intermediate Production

    This material serves as a specialized aromatic intermediate for synthesizing disperse and acid dyes, which require precise substitution patterns on the benzene ring for lightfastness and washfastness in technical textiles. The compound’s controlled substitution allows for color shade modulation in azo and anthraquinone dye production, and formulators adjust its usage based on target chromophore structure and final application endurance requirements.

    Industry compliance standards

    • OEKO-TEX® Standard 100 – Certification for hazardous material exclusion
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • REACH Annex XVII – Restriction on azo dye precursors
    • ISO 9001:2015 for production and batch traceability

    Typical usage ratio

    • Loaded at 0.5–3% of total dye mass, dependent on the chromophore class and color depth targeted by dye chemists

    Downstream process integration

    • Fed into initial azo coupling or acylation reactions for constructing dye intermediates with direct feed to distillation and purification units before downstream finishing

    Final product types

    • Disperse dyes for synthetic fiber coloration (polyester, acetate)
    • Acid dyes used in nylon and wool processing
    • Anthraquinone derivatives for high-temperature textile applications
    • Reactive dye intermediates for trichromatic and specialty shade solutions

    4. Fine Chemicals and Specialty Intermediates

    Chemical manufacturers utilize the compound in the synthesis of specialty aromatic intermediates, where electron-withdrawing and -donating group interplay is necessary for constructing customized molecules used in polymer electronics, photoresist agents, and advanced materials R&D. Its controlled reactivity enables precise site-selective functionalization, directly affecting downstream catalytic, propellant, or coating performance as required by specialty chemical designers.

    Industry compliance standards

    • ISO 14001:2015 for environmental management in specialty chemicals
    • Custom QC protocols based on customer’s integration process specifications
    • REACH compliance for intermediate status in EU supply chains
    • RoHS Directive (EU) 2015/863 for electrical/electronic material applications

    Typical usage ratio

    • Reactant feed of 1.5–5% weight of target intermediate, with process control based on downstream electronic or coating physicochemical requirement

    Downstream process integration

    • Charged into Grignard or Friedel–Crafts-type synthesis units, followed by selective reduction or alkylation depending on customer-specified final product characteristics

    Final product types

    • Functional intermediates for OLED and conductive polymer research
    • Photoresist precursors for microelectronics lithography
    • Specialty coating additives for industrial surfaces
    • R&D scale reference compounds for analytical and materials testing

    5. Chemical Synthesis Reference Material Supply

    Research institutions and contract manufacturing organizations employ the material as a certified reference compound for method validation, trace impurity identification, and synthetic process development. High-purity, lot-specific supply supports analytical laboratories and custom small-batch process scale-ups requiring consistent baseline material for regulatory filings, material corestructural elucidation, and control sample establishment.

    Industry compliance standards

    • ISO/IEC 17025 test laboratory accreditation for certified reference materials
    • USP General Chapter <1224> on reference standards
    • GLP (Good Laboratory Practice) guidelines for process development
    • Sigma-Aldrich/analytical chemistry supplier requirements for calibration material

    Typical usage ratio

    • Applied at 0.1–0.25% by weight or as a 1–5 mg control standard per analytical validation sample, as specified by protocol for method comparison or instrumentation calibration

    Downstream process integration

    • Supplied to analytical labs for HPLC, GC-MS method validation, or as a spike for process impurity tracking; incorporated as a benchmark in pilot-scale or scale-up extractive recovery for process optimization studies

    Final product types

    • Analytical calibration standards for chemical QC
    • Reference batches for synthetic method validation packages
    • Process control spikes for impurity/contaminant screening
    • Stability control samples for batch release testing in regulated manufacturing
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