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2-Methoxy-5-Nitroaniline Hydrochloride

    • Product Name 2-Methoxy-5-Nitroaniline Hydrochloride
    • Alias 2-Methoxy-5-nitrobenzenamine hydrochloride
    • Einecs 629-414-7
    • 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
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    Specifications

    HS Code

    401815

    Product Name 2-Methoxy-5-Nitroaniline Hydrochloride
    Cas Number 50292-01-4
    Molecular Formula C7H9ClN2O3
    Molecular Weight 204.62 g/mol
    Appearance Yellow to orange solid
    Melting Point 154-158°C (decomposes)
    Solubility Soluble in water
    Storage Temperature Store at 2-8°C
    Purity Typically ≥98%
    Synonyms 2-Methoxy-5-nitroaniline hydrochloride; o-Anisidine-5-nitro hydrochloride
    Hazard Class Irritant

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

    Packing & Storage
    Packing Amber glass bottle with screw cap, labeled “2-Methoxy-5-Nitroaniline Hydrochloride, 25g, for laboratory use only, hazard warnings.”
    Shipping 2-Methoxy-5-Nitroaniline Hydrochloride is shipped in airtight, chemical-resistant containers, clearly labeled and securely packed to prevent leakage. Shipping complies with international regulations for hazardous substances, typically under controlled temperature and humidity. Safety data sheets (SDS) accompany the shipment to ensure safe handling during transport and upon delivery.
    Storage 2-Methoxy-5-nitroaniline hydrochloride should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers and bases. Keep it protected from light and moisture, as it may be sensitive to both. Store at room temperature and ensure proper chemical labeling is in place to avoid accidental misuse.
    Application of 2-Methoxy-5-Nitroaniline Hydrochloride

    Applications of 2-Methoxy-5-Nitroaniline Hydrochloride in Industrial Manufacturing

    As a specialized manufacturer, we supply 2-Methoxy-5-Nitroaniline Hydrochloride to a tightly defined group of industrial downstream sectors. This intermediate finds its place in sophisticated organic syntheses, supporting the production of high-grade specialty materials where quality standards, precise dosing, and controlled process integration are critical. Below, we detail its established industrial deployment across key application scenarios.

    1. Synthesis of Azo Dyes for Polyester and Nylon Textiles

    Textile dye manufacturers use our material as a diazo component for producing high-performance yellow and orange azo dyes, especially formulated for synthetic fiber applications. The hydrochloride salt permits direct dissolution during coupling, supporting rigorous batch consistency and enabling reproducibility between production lots. This application demands strict alignment with global textile chemical directives and robust in-process controls to ensure low impurity levels, which is vital for downstream dyehouses serving apparel, upholstery, and technical textile sectors.

    Industry compliance standards

    • EU REACH Regulation (EC) No 1907/2006 - Dye and chemical safety reporting
    • ZDHC MRSL (Zero Discharge of Hazardous Chemicals Manufacturing Restricted Substances List)
    • Oeko-Tex Standard 100 Annex 4 - Dye-related residue limits
    • GB/T 3339-2012 - China national textile dye quality benchmark

    Typical usage ratio

    • Concentration in diazo dye synthesis: 8% to 16% m/m based on targeted chromophore structure (adjusted per fibre affinity requirements)

    Downstream process integration

    • Introduced in initial diazotization and coupling stage; forms the primary aromatic source for azo bond formation.

    Final product types

    • Disperse dyes for polyester (e.g. yellow disperse 42, orange disperse 44 series)
    • Acid dyes used in nylon yarn dyeing
    • Non-ionic dye intermediate blends for microfibre textiles
    • Technical textile dye formulations (e.g. for automotive fabrics)

    2. Pharmaceutical Intermediate for Anti-Tuberculosis Drug Synthesis

    Leading pharmaceutical synthesis contractors employ this compound as a core intermediate in the route towards the preparation of rifamycin and related antibiotics. Its pure crystalline form ensures high reproducibility in subsequent coupling and ring-closure stages, supporting batch-to-batch traceability demanded by regulatory audits. Consistent material attributes such as particle size distribution and impurity profile are maintained to enable predictable conversion rates in multi-step active pharmaceutical ingredient (API) synthesis routes.

    Industry compliance standards

    • USP-NF (United States Pharmacopeia–National Formulary) for API intermediates
    • ICH Q7 GMP for Active Pharmaceutical Ingredients
    • WHO GMP guidelines for intermediates
    • EDQM Certificate of Suitability to the monographs of the European Pharmacopoeia (CEP)

    Typical usage ratio

    • Integrated at 5% to 10% molar basis per API synthesis batch, recalculated depending on target antibiotic molecule

    Downstream process integration

    • Charged during aromatic nitration and subsequent amide/condensation reactions, laying groundwork for macrocyclic core construction.

    Final product types

    • Rifampicin (anti-tuberculosis API)
    • Rifamycin SV and derivatives
    • Other nitroaniline-derived antibiotic intermediates

    3. Raw Material for Optical Brightener Manufacturing in Paper Industry

    Pulp and specialty paper chemical producers select this material as a nitroaromatic precursor when synthesizing stilbene-based optical brightening agents. Its high purity and low ash content contribute to enhanced brightness and UV-stability in end-use paper grades, especially for coated and office paper types. Downstream formulating operations require this intermediate to present minimal trace-metal content to avoid shade darkening and maintain fluorescence across high-volume production lines.

    Industry compliance standards

    • EN 646:2018 (Migration Of Colours) for food contact paper
    • TAPPI T524 for optical brightening characterization
    • ISO 287: Paper and board - Moisture content test protocols
    • FDA 21 CFR Part 176.170 - Food contact regulations for chemicals used in paper

    Typical usage ratio

    • 0.3% to 1.5% by weight in brightener precursor synthesis, with adjustments for paper weight and required fluorescence intensity

    Downstream process integration

    • Fed to initial nitration step in brightener precursor line; participates in multi-step reduction and cyclization leading to the active optical agent.

    Final product types

    • Fluorescent whitening agents for copy and print papers
    • Paperboard brightener concentrates for packaging
    • Luminescent agents for security and anti-counterfeit paper products

    4. Intermediate for Agx Color Photographic Coupler Synthesis

    Producers of silver halide photographic materials use this hydrochloride as an aromatic amino building block in the synthesis of magenta and yellow coupler components. The controlled reactivity of the para-nitro and ortho-methoxy groups aligns with photochemical stability requirements, while downstream quality protocols demand consistent spectral purity and low halide residue. Its careful handling in the coupler functionalization stages ensures high-resolution image performance in both film and paper products.

    Industry compliance standards

    • ISO 9001 for specialty chemical batch reproducibility
    • ISO 3664:2009 - Viewing conditions for image assessment
    • ANSI IT9.2-1998 - Photographic stability and process chemicals
    • Internal photographic-grade QC (grain size, absorbance specification)

    Typical usage ratio

    • 0.5% to 3% by mass in the synthesis of color coupler intermediates, varied by targeted spectral response and light sensitivity

    Downstream process integration

    • Added during aromatic substitution stages; further processed through acylation or sulfonation prior to coupler attachment

    Final product types

    • AgX-based color print paper emulsions
    • Professional camera film color dye couplers
    • Photographic paper for archival and commercial processing

    5. Precursor for Liquid Crystal Display (LCD) Alignment Layer Syntheses

    Display material producers source this compound to build specialty polyimide and polyamide alignment layers, where the nitroaniline motif contributes to surface orientation properties. The high solubility of the hydrochloride form supports polymerization with precise batch charge measurement, while technical datasheets demand traceability of aromatic source to ensure downstream electrical and optical uniformity. Application in cleanroom environments necessitates meticulous control of contaminant content and consistency of melting point.

    Industry compliance standards

    • IEC 62341 (Organic electronic displays material standards)
    • RoHS Directive 2011/65/EU (Restriction of Hazardous Substances)
    • ISO 14644-1 (Cleanroom performance for display chemicals)
    • ASTM D883 for polyimide material characteristics

    Typical usage ratio

    • Ranges from 0.8% to 2.3% by monomer unit weight in alignment polymer precursor mixes, depending on desired anchoring energy and LCD type

    Downstream process integration

    • Charged at the monomer functionalization stage in polyimide synthesis; remains as a covalently bound motif in the polymer backbone applied to glass substrates

    Final product types

    • Alignment coatings for TFT-LCD panels
    • Polyimide films for active matrix displays (OLED, LCD, E-paper)
    • In-plane switching (IPS) display panel alignment materials
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