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4-(Morpholinomethyl)Aniline

    • Product Name 4-(Morpholinomethyl)Aniline
    • Alias p-(Morpholinomethyl)aniline
    • Einecs 652-230-4
    • 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

    616862

    Product Name 4-(Morpholinomethyl)Aniline
    Cas Number 2524-37-0
    Molecular Formula C11H16N2O
    Molecular Weight 192.26
    Appearance White to off-white solid
    Melting Point 93-97°C
    Solubility Soluble in organic solvents
    Purity Typically ≥98%
    Synonyms p-(Morpholinomethyl)aniline; 4-(Morpholin-4-ylmethyl)aniline
    Smiles c1ccc(cc1N)CN2CCOCC2
    Inchi InChI=1S/C11H16N2O/c12-10-3-1-9(2-4-10)8-13-5-7-14-6-13/h1-4H,5-8,12H2
    Storage Temperature 2-8°C

    As an accredited 4-(Morpholinomethyl)Aniline factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing White plastic bottle labeled "4-(Morpholinomethyl)Aniline, 100g" with black screw cap, hazard symbols, lot number, and safety instructions.
    Shipping 4-(Morpholinomethyl)aniline should be shipped in tightly sealed containers, protected from moisture and light. Transport under ambient temperature, following all applicable chemical regulations. Ensure appropriate hazard labeling and include safety documentation. Handle with care to avoid leaks or spills, and keep away from incompatible substances such as oxidizing agents.
    Storage Store 4-(Morpholinomethyl)aniline in a tightly sealed container, protected from light and moisture, in a cool, dry, and well-ventilated area. Keep away from incompatible materials such as strong oxidizing agents and acids. Ensure appropriate labeling and restrict access to trained personnel. Follow all safety procedures, using personal protective equipment as recommended in the safety data sheet (SDS).
    Application of 4-(Morpholinomethyl)Aniline

    Applications of 4-(Morpholinomethyl)Aniline in Industrial Manufacturing

    4-(Morpholinomethyl)Aniline serves as a value-added intermediate across several established industrial sectors. Its structure fits demanding synthesis workflows, where precise control over purity, reactivity, and end-use compatibility is essential. Below, we detail primary sectors based on true market adoption, providing application context, regulatory standards, technical ratios, production workflow, and finished product categories.

    1. Synthesis of Agrochemical Active Ingredients

    Major crop protection manufacturers select this compound as a key amine building block during the final stages of active ingredient synthesis, especially for phenylurea and phenylcarbamate herbicides. Its inclusion ensures reliable performance under scalable, multi-ton batch protocols. Formulators adjust concentration based on desired substitution patterns and reaction yield targets, often under tightly controlled pH and solvent conditions to meet industry regulations for purity, residuals, and by-products.

    Industry compliance standards

    • ISO 9001-certified QC protocols for batch reproducibility
    • Good Manufacturing Practice (GMP) for agricultural chemicals
    • REACH Annex IX substance registration and risk assessment
    • OECD Test Guidelines for pesticide raw material screening

    Typical usage ratio

    • 8%–15% by weight relative to total reactants in final condensation or coupling steps; adjusted according to substitution demands and impurity tolerances defined by the target active

    Downstream process integration

    • Integrated as a final amination or alkylation reactant following chlorination or nitro reduction stages, processed via multi-stage stirred-tank reactors under inert gas

    Final product types

    • Herbicide actives (e.g., certain phenylurea derivatives for Pre/Post-emergence control)
    • Fungicide intermediates under custom synthesis
    • Insecticide raw materials with substituted aniline moieties
    • Custom pesticide formulation blocks for large-scale agricultural use

    2. Pharmaceutical Intermediate for Small Molecule Synthesis

    Our material is integrated by pharmaceutical process chemistry groups during the preparation of advanced intermediates for select APIs and laboratory reference standards. The compound’s morpholino group confers increased polarity and hydrogen bond capacity, relevant for final API functionalization. Formulation follows validated cGMP pathways, with batch-level trace analysis and impurity profiling conducted per ICH standards to ensure patient safety and regulatory alignment in finished drug substances.

    Industry compliance standards

    • ICH Q7A Good Manufacturing Practice Guidance for Active Pharmaceutical Ingredients
    • USP/NF and Ph. Eur. monographs for analytical control
    • FDA and EMA registration dossier requirements
    • ISO 13485 support systems where applied

    Typical usage ratio

    • 5%–13% mole equivalent in amide coupling, nucleophilic aromatic substitution, or reductive amination steps executed at 1–10 kg/batch pilot plant scale; variation based on stoichiometry and route-specific impurity thresholds

    Downstream process integration

    • Charged after upstream aryl halogen or nitro precursor formation, reacts under mild or moderately basic conditions, typically in polar aprotic media, followed by workup and chromatographic purification as required for final intermediate isolation

    Final product types

    • Pharmaceutical intermediates for kinase inhibitors
    • Precursors for bactericidal or CNS-active APIs
    • Custom R&D libraries for biotech lead optimization
    • Reference standards used in analytical method validation

    3. Specialty Dye and Pigment Synthesis

    Colorant synthesis specialists incorporate this amine into multi-step production workflows for azo and methine dye intermediates. The compound’s aromatic and polar substituents provide tunable chromophore properties, impacting fastness and shade under various textile and ink systems. Strict control of reaction parameters enables maximum yield and finished dye reproducibility, in line with international environmental and product safety regulations.

    Industry compliance standards

    • OEKO-TEX Standard 100 for restricted substance lists in finished dyes
    • REACH and GHS hazard communication for dye intermediates
    • ZDHC Manufacturing Restricted Substances List (MRSL)
    • ISO 14001 environmental management as required by top-tier pigment users

    Typical usage ratio

    • 9%–20% relative to diazonium counterpart in diazotization and coupling reactions, varied based on chromophore complexity and desired application fastness; ratios optimized after pilot plant trials

    Downstream process integration

    • Metered into coupling vessel immediately after diazotization, under strictly regulated pH and temperature, followed by purification, crystallization, and standardization per customer color panel requirements

    Final product types

    • Synthetic azo dyes for industrial textiles
    • Specialty pigments for inkjet and offset inks
    • Colorant intermediates for plastics compounding
    • Reactive dyes in custom application formulations

    4. Epoxy Curing Agent and Crosslinker in Industrial Coatings

    Epoxy resin formulators use this compound as a latent curing agent or crosslinker to improve coating durability and chemical resistance. Its reactivity and solubility support tailored cure dynamics and minimize blush or film defects, especially in high-solids and waterborne coatings. Usage complies with advanced performance norms for protective and functional coatings applied in automotive, marine, and industrial sectors.

    Industry compliance standards

    • ISO 12944 (Corrosion Protection of Steel Structures by Protective Paint Systems)
    • ASTM D3023 (Polymer Surface Coating Specifications)
    • RoHS (Restriction of Hazardous Substances) for coatings
    • DIN EN 1504-2 compliance for concrete protective coatings in Europe

    Typical usage ratio

    • 2.5%–7.5% by resin weight; tuning depends on epoxy system type, desired crosslink density, and working pot life; evaluated by laboratory cure profile and user-specific application testing

    Downstream process integration

    • Premixed with epoxy prepolymers during formulation blend; introduced during grinding or pre-dispersion, then processed via high-shear mixers or dispersers prior to application or canning

    Final product types

    • Two-component epoxy coating hardeners
    • Industrial floor and anti-corrosive coatings
    • Marine and automotive primer additives
    • Protective sealants for civil engineering structures
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