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4-Iodobenzylamine

    • Product Name 4-Iodobenzylamine
    • Alias 4-Iodobenzenemethanamine
    • Einecs 612-219-4
    • 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
    VTB
    Specifications

    HS Code

    621959

    Cas Number 5369-65-3
    Molecular Formula C7H8IN
    Molecular Weight 233.05 g/mol
    Appearance White to off-white solid
    Melting Point 65-69°C
    Density 1.77 g/cm³ (approximate)
    Purity Typically ≥98%
    Solubility Soluble in DMSO, dimethyl formamide; slightly soluble in water
    Synonyms 4-Iodobenzenemethanamine, p-Iodobenzylamine
    Smiles C1=CC(=CC=C1CN)I
    Inchi Key VJNRAUWQFGGFQK-UHFFFAOYSA-N

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

    Packing & Storage
    Packing 4-Iodobenzylamine, 25g: Supplied in an amber glass bottle, tightly sealed with a screw cap, labeled with safety and identification information.
    Shipping 4-Iodobenzylamine is shipped in tightly sealed containers, protected from light, moisture, and incompatible substances. It is transported as a hazardous material in compliance with international regulations, requiring appropriate labeling and documentation. Temperature and handling guidelines must be followed to ensure chemical stability and personnel safety during transit.
    Storage 4-Iodobenzylamine should be stored in a tightly sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizers. Store at room temperature and protect from moisture. Ensure proper labeling and keep away from sources of ignition. Use appropriate chemical storage cabinets and follow all relevant safety regulations for hazardous chemicals.
    Application of 4-Iodobenzylamine

    Applications of 4-Iodobenzylamine in Industrial Manufacturing

    Our production of 4-Iodobenzylamine supplies active downstream manufacturers with a high-purity intermediate tailored for demanding industrial syntheses. The following sections outline real-world applications where this raw material plays an essential role in advanced fine chemical, pharmaceutical, and material manufacturing processes, strictly aligning with relevant compliance and formulation protocols.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    4-Iodobenzylamine functions as a synthesis intermediate for several pharmaceutical actives, primarily in the preparation of benzylamine-derived APIs including selective serotonin receptor antagonists and certain investigational oncology agents. Manufacturers employ it in condensation and substitution reactions, where its iodo group introduces selective reactivity essential for constructing complex molecular scaffolds. Quality assurance teams ensure traceability and impurity profiles meet global regulated market requirements during each production campaign.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice Guidance for APIs
    • US FDA cGMP (21 CFR Parts 210/211)
    • European Pharmacopoeia (EP) standards for intermediates
    • Chinese Pharmacopeia (ChP) quality specifications

    Typical usage ratio

    • Employed at 1.0–2.5 molar equivalents as a limiting or excess reagent, dependent on target molecule and impurity control requirements.

    Downstream process integration

    • Added during protected amine coupling steps or halogen exchange sequences, normally under anhydrous or inert conditions to control side reactions.

    Final product types

    • Bulk pharmaceutical intermediates (e.g., substituted benzylamines)
    • Small-molecule drug candidate ingredients
    • APIs for oncology and CNS treatments

    2. Agrochemical Synthesis Feedstock

    R&D and commercial agricultural chemical producers incorporate 4-Iodobenzylamine in the multi-step synthesis of benzylic pesticide intermediates, particularly for fungicides and plant growth regulation agents. The precise functional group enables site-selective modifications in aromatic ring transformations, supporting consistent batch quality and process scale-up for field applications. Production teams focus on controlled addition and reagent compatibility to minimize process deviations.

    Industry compliance standards

    • OECD Principles of Good Laboratory Practice (GLP)
    • FAO/WHO Specifications for Agricultural Pesticides
    • REACH Registration (EC 1907/2006) for European downstream users
    • ISO 9001 certified quality management systems

    Typical usage ratio

    • Formulations usually use 0.8–1.3 molar equivalents, optimized according to crop safety, active ingredient yield, and regulatory residue limits.

    Downstream process integration

    • Injected during early-stage aromatic amination or halide exchange steps under strictly monitored conditions to reduce byproduct formation.

    Final product types

    • Active pesticide intermediates
    • Fungal growth regulators
    • Plant growth stimulant precursors

    3. Functional Dye and Pigment Intermediate

    The specialty colorant sector utilizes this raw material in the design and synthesis of advanced functional dyes, including those for OLED and organic semiconductor manufacturing. 4-Iodobenzylamine enables the introduction of amine moieties into aromatic backbones, tuning charge mobility and color properties for display technology and technical textile coatings. Manufacturing engineers oversee reaction conditions using this intermediate to achieve required chromatic uniformity and thermal stability in final dispersions.

    Industry compliance standards

    • EN 71-3 (European Toy Safety Standard for colorants)
    • REACH Annex XVII restrictions on halogenated intermediates
    • ISO 9001 certified pigment quality management
    • OEKO-TEX Standard 100 for textile applications

    Typical usage ratio

    • Typically integrated at 0.5–1.8 molar equivalents depending on chromophore design and required functional group density.

    Downstream process integration

    • Added in the condensation or nucleophilic substitution step to generate precursor amines that undergo further coupling into extended conjugated systems.

    Final product types

    • Organic electronic dyes
    • Technical textile colorants
    • Specialty pigment dispersions

    4. Cross-Linking Agent in Polymer Modification

    Manufacturers of specialty polymers and resins use 4-Iodobenzylamine as a functional cross-linking agent, particularly for introducing amine functionality into aromatic or mixed-polymer networks. This provides enhanced mechanical and adhesive properties for coatings, adhesives, and engineered composites. Process chemists fine-tune dosage and feeding sequence to improve cure efficiency and end-use performance under established regulatory environments.

    Industry compliance standards

    • ISO 9001 Quality Management for specialty polymers
    • RoHS Directive (2011/65/EU) on restriction of hazardous substances
    • REACH compliance for industrial polymers
    • UL 94 flammability standards for finished plastics

    Typical usage ratio

    • Usually added at 0.2–1.0% w/w of total polymer mass, optimized for network density and mechanical specifications of the target resin system.

    Downstream process integration

    • Introduced during pre-polymer mixing or melt-compounding, reacting through nucleophilic substitution with compatible monomer units or functionalized chain ends.

    Final product types

    • Cross-linked adhesive resins
    • Functionalized engineering plastics
    • Surface-modified polymer coatings

    5. Custom Fine Chemical Intermediate for Research and Development

    Contract manufacturing organizations (CMOs) and specialty fine chemical producers deploy 4-Iodobenzylamine as an advanced intermediate for structure-activity studies, ligand design, and pilot-scale syntheses of novel compounds under confidential R&D programs. The precise iodo substitution offers unique selectivity in amination, bioconjugation, or radio-labeling techniques, while R&D chemists adjust synthetic routes and analytical protocols to match evolving project requirements.

    Industry compliance standards

    • ISO 17025 Laboratory Accreditation
    • OECD GLP for compound characterization
    • Responsible Care QC protocols
    • Material Safety Data Sheet (MSDS) regulatory documentation

    Typical usage ratio

    • Amount varies from 20 mg to >500 g per batch, proportional to lab scale, screening array, and purity control targets.

    Downstream process integration

    • Charged as a unique building block or labeling agent in solution-phase or solid-phase synthesis workflows, frequently under inert gas and anhydrous conditions.

    Final product types

    • Novel heterocyclic intermediates for patent research
    • Specialty ligands for catalyst screening
    • Radio-labeled compounds for tracer and imaging studies
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