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3-Phenyl-4-Methoxyaniline Hydrochloride

    • Product Name 3-Phenyl-4-Methoxyaniline Hydrochloride
    • Alias 3-Phenyl-4-methoxybenzenamine hydrochloride
    • Einecs 629-125-3
    • 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

    778231

    Product Name 3-Phenyl-4-Methoxyaniline Hydrochloride
    Cas Number 1421367-96-1
    Molecular Formula C13H14ClNO
    Molecular Weight 235.71 g/mol
    Appearance Off-white to pale yellow solid
    Melting Point 189-193°C
    Solubility In Water Moderate
    Purity Typically ≥98%
    Storage Temperature 2-8°C
    Synonyms 4-Methoxy-3-phenylaniline hydrochloride
    Chemical Class Aromatic amine hydrochloride salt

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

    Packing & Storage
    Packing White, opaque plastic bottle labeled "3-Phenyl-4-Methoxyaniline Hydrochloride, 25g," with hazard symbols, lot number, and storage instructions.
    Shipping 3-Phenyl-4-Methoxyaniline Hydrochloride is shipped in tightly sealed, chemically resistant containers to prevent moisture and contamination. The packaging complies with regulatory standards for chemical transport. It is handled and labeled as a laboratory chemical, requiring cool, dry storage and protection from light during transit. Suitable documentation accompanies all shipments.
    Storage **Storage Description for 3-Phenyl-4-Methoxyaniline Hydrochloride:** Store in a tightly sealed container, protected from light and moisture, in a cool, dry, well-ventilated area. Keep away from incompatible materials such as strong oxidizing agents. Avoid prolonged exposure to air. Ensure appropriate labeling and restrict access to authorized personnel. Refer to the Safety Data Sheet (SDS) for detailed handling and storage guidelines.
    Application of 3-Phenyl-4-Methoxyaniline Hydrochloride

    Applications of 3-Phenyl-4-Methoxyaniline Hydrochloride in Industrial Manufacturing

    3-Phenyl-4-Methoxyaniline Hydrochloride serves essential roles in several key industrial sectors. We supply this intermediate directly to global manufacturers, supporting strict regulatory compliance and process optimization across diverse chemical domains. The following sections outline primary downstream use cases, industry standards, formulation parameters, process stages, and commercial finished products relevant to our customers’ operations.

    1. Pharmaceutical Intermediate for Active Pharmaceutical Ingredient Synthesis

    This compound functions as a vital aniline intermediate in the multi-step synthesis of APIs, especially within antihypertensive and anticancer drug manufacturing. Process chemists utilize it in nucleophilic aromatic substitution reactions for custom building block assembly, supporting specific pathway requirements set by final API design. Our technical service team routinely coordinates with client QA/QC departments to meet batch consistency, impurity management, and traceability needs stipulated for regulated pharmaceutical production.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • USP-NF and European Pharmacopoeia monographs for starting materials
    • 21 CFR Part 210/211 (FDA cGMP for finished pharmaceuticals where applicable)
    • Chinese Pharmacopoeia (for local API producers)

    Typical usage ratio

    • Batch reactions typically employ 3-Phenyl-4-Methoxyaniline Hydrochloride at 0.85–1.20 molar equivalents relative to core aldehyde/halide precursors. Operators adjust the ratio based on target yield, impurity profile, and downstream conversion efficiency as validated during process development.

    Downstream process integration

    • Charged to anhydrous or aqueous reactors following in situ generation of acid halides or coupling agents.
    • Enters multi-step synthesis before final salt formation and crystallization opposition.
    • Material tracking begins at this input stage for full GMP serialization.

    Final product types

    • Antihypertensive APIs (e.g., imidazoline, quinazoline class compounds)
    • Intermediates for kinase or immunomodulator APIs
    • Key pharmaceutical building blocks for global drug substance manufacturers

    2. Advanced Dye Intermediate in Specialty Colorant Manufacture

    Downstream dyestuff manufacturers use this material as a critical aromatic amine component in synthesizing azo and anthraquinone dye molecules. Its phenyl and methoxy substituents facilitate color tuning and solubility control for advanced textile, leather, and plastics coloration. Chemical engineers closely manage impurity and meta-position substitution to achieve high color fastness and application-specific chromatic performance in finished colorants.

    Industry compliance standards

    • OEKO-TEX® Standard 100 (textile dyes authorization)
    • REACH Annex XVII (EU restrictions on aromatic amines and related intermediates)
    • ZDHC Manufacturing Restricted Substances List
    • ISO 9001:2015 (for traceability in colorant manufacturing)

    Typical usage ratio

    • Initial coupling steps typically utilize 5–15% by weight relative to base diazotized components, modifiable by color intensity and molecular weight targets within individual dye recipes.

    Downstream process integration

    • Charged after sulfonation or nitration of the base aromatic skeleton.
    • Integrates into the diazotization process, providing the functional amine group for further reaction steps.
    • Purification by chromatographic or crystallization methods prior to final dye formulation.

    Final product types

    • Azo dyes for polyester and polyamide fibers
    • Anthraquinone dyes for high-brightness coloration
    • Specialty pigments for automotive coatings and plastic masterbatches

    3. Functional Monomer Sourcing for Polymer Modification

    Advanced polymer manufacturers leverage this aniline derivative as a functional group donor for custom polymer modification. Its aromatic ring system and electron-donating substituents enable fine-tuning of thermal properties, solubility, and electrical conductivity of specialty resins. The hydrochloride form ensures better solubility and charging control within polymerization reactors, supporting consistent batch homogeneity and downstream material quality for high-performance engineering plastics and coatings.

    Industry compliance standards

    • ISO 14001 (polymer plant environmental management systems)
    • ROHS 3 (EU Directive on permissible amine and monomer residuals for electronics-use plastics)
    • ASTM D256 (for impact and mechanical performance verification)
    • UL 94 (flame retardancy for finished polymers, where functionalized)

    Typical usage ratio

    • Utilized at 0.5–3.0% by polymer mass, adjusted by desired end-use modification and resin type. Process R&D determines introduction levels to balance flow characteristics with targeted electrical or thermal profile adjustments.

    Downstream process integration

    • Introduced in pre-polymer mixing prior to chain extension, typically after initiator charging but before bulk monomer addition.
    • Functionalizes the polymer backbone via copolymerization or post-grafting steps, depending on desired material modification.
    • Residue analysis and off-gas monitoring implemented at this stage to ensure compliance and safe operation.

    Final product types

    • Antistatic engineering plastics for electronics housings
    • Heat-stable specialty coatings
    • Conductive polymer films and sheets for printed circuit board manufacturing

    4. Intermediate in Agrochemical and Plant Growth Regulator Synthesis

    Our industrial partners in the crop protection sector apply this compound for the synthesis of phenyl-based agrochemical actives and select plant growth regulators. The aromatic amine structure enables tailored halogenation and alkylation routes during plant-active molecule assembly. Compliance with agricultural chemical manufacturing directives and residue monitoring is strictly managed due to sensitive end-use in regulated field environments. Specialist formulation chemists coordinate with our technical team to align input handling with each downstream formulation’s application and safety requirements.

    Industry compliance standards

    • FAO Specifications for Plant Protection Products
    • ISO 17025 (agrochemical residue laboratory validation)
    • US EPA 40 CFR Part 165 (for active ingredient production and container management)
    • Global GAP (relevant for farm-applied plant growth regulator ingredients)

    Typical usage ratio

    • Dosage input from 2–10% w/w of total input mass in precursor synthesis stage, regulated by required purity and target residue specifications of the final plant-active compound.

    Downstream process integration

    • Used as a primary amine during initial condensation and derivatization reactions.
    • Enters before chlorination or oxidative cyclization in active synthesis train.
    • Process sampling for QC verification occurs post-integration prior to active substance isolation.

    Final product types

    • Aromatic herbicide intermediates
    • Synthetic auxin and cytokinin regulators
    • Precursor materials for phenylurea-based plant growth inhibitors
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