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5-Amino-2,4,6- Triiodisophthaloyl Acid Dichloride

    • Product Name 5-Amino-2,4,6- Triiodisophthaloyl Acid Dichloride
    • Alias 5-Amino-2,4,6-triiodoisophthaloyl chloride
    • Einecs 629-010-9
    • 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

    546348

    Molecular Formula C8H2Cl2I3NO3
    Molecular Weight 626.73 g/mol
    Appearance Pale yellow to light brown powder
    Melting Point Decomposes without a clear melting point
    Purity Typically >98%
    Solubility Insoluble in water; soluble in organic solvents like dichloromethane
    Boiling Point Decomposes before boiling
    Storage Conditions Store in cool, dry place; keep tightly closed under inert gas
    Reactivity Reacts with water to liberate hydrochloric acid
    Functional Groups Acyl chloride, amino, aromatic, triiodo
    Hazard Statements Corrosive; causes severe skin burns and eye damage

    As an accredited 5-Amino-2,4,6- Triiodisophthaloyl Acid Dichloride factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing The 100g bottle of 5-Amino-2,4,6-Triiodisophthaloyl Acid Dichloride arrives in a sealed amber glass bottle with hazard labeling.
    Shipping 5-Amino-2,4,6-Triiodoisophthaloyl Acid Dichloride should be shipped in tightly sealed containers, protected from moisture and light, and placed in secondary containment for added safety. It must be labeled as a hazardous chemical, and transported according to relevant chemical regulations, with all necessary safety documents and material safety data sheets included.
    Storage 5-Amino-2,4,6-Triiodoisophthaloyl Acid Dichloride should be stored in a tightly sealed container under a dry, inert atmosphere, such as nitrogen or argon, in a cool, well-ventilated area away from moisture, heat, and incompatible substances like strong bases and oxidizers. Protect from light and humidity to prevent decomposition and hydrolysis. Label the container clearly and use secondary containment for extra safety.
    Application of 5-Amino-2,4,6- Triiodisophthaloyl Acid Dichloride

    Applications of 5-Amino-2,4,6-Triiodisophthaloyl Acid Dichloride in Industrial Manufacturing

    5-Amino-2,4,6-Triiodisophthaloyl Acid Dichloride is primarily utilized in advanced life-science, medical diagnostics, high-resolution imaging, and specialty polymer sectors. As a direct manufacturer, we supply this compound to downstream users who require high-purity intermediates for the synthesis of high‐performance materials where the introduction of triiodoaromatic functionality and controlled amide/acid chloride reactivity are essential. Below, we have outlined the principal industrial application segments, highlighting relevant compliance systems, formula inclusion levels, integration within the respective production processes, and the finalized goods that incorporate this specialty chemical.

    1. X-ray Contrast Media Intermediate Production

    The high halogenation level and amine functionalization enable downstream manufacturers to synthesize amphiphilic building blocks for advanced X-ray contrast agents. This material enters the process as a key step for iodinated aromatic structures demanded by pharmaceutical imaging. Active QC for halogen content and functional purity is a hallmark of this application.

    Industry compliance standards

    • ICH Q7 API GMP for intermediates
    • USP, Ph. Eur., JP (where used in final API synthesis)
    • 21 CFR Part 211 (if exposed to regulated drug manufacturing)
    • ISO 9001:2015 Quality Management (process control)

    Typical usage ratio

    • Entry concentrations typically range from 0.2–0.35 molar equivalents per halogenated intermediate batch, adjusted for targeted degree of iodination and batch size scale.

    Downstream process integration

    • Chloride-amine condensation phase following activation of carboxylic groups, with subsequent quenching, filtration, and purification before onward coupling in the X-ray contrast agent core synthesis.

    Final product types

    • Iodinated non‐ionic contrast media precursors (e.g., iohexol, iopamidol intermediates)
    • API-grade building blocks for radiology chemicals

    2. Biomedical Imaging Polymer Matrix Synthesis

    5-Amino-2,4,6-Triiodisophthaloyl Acid Dichloride serves as a high-density iodinated monomer in the production of polymer matrices for biomedical imaging. It is especially valued in the copolymerization with PEG/PEI or polysaccharide derivatives, offering precisely controlled iodine incorporation for advanced medical diagnostic platforms.

    Industry compliance standards

    • ISO 13485:2016 (Medical device QMS, where polymer is device component)
    • REACH registered for use in polymer applications in the EU
    • Biocompatibility—ISO 10993 testing (for devices)
    • USP Class VI plastics standards (for contact applications)

    Typical usage ratio

    • Used at 1.5–8 wt% of total monomer charge, fine-tuned for desired X-ray opacity and mechanical properties of the resulting polymer blend.

    Downstream process integration

    • Introduced during co-polymerization in solvent phase, often under nitrogen, before film casting, molding, or extrusion for further fabrication into imaging consumables or device components.

    Final product types

    • X-ray opaque polymer films for catheter tips and guidewires
    • Contrast-enhanced scaffold materials for 3D imaging studies
    • Medical component inserts for surgical visualization

    3. Specialty Polyamide Synthesis for High-Density Functional Materials

    By leveraging its bifunctional amine and acid chloride moieties, downstream processors employ this compound to synthesize triiodinated polyamides and polyimides exhibiting increased density, radiation resistance, and identifiable signatures suitable for demanding industries. Integration occurs in systems requiring both chemical toughness and radiopacity.

    Industry compliance standards

    • ISO 9001:2015 (General QMS for engineering plastics)
    • RoHS Directive (2011/65/EU, for electrical/electronic parts)
    • EN 60216 (for thermal endurance where required)

    Typical usage ratio

    • Incorporated at 0.5–3.5 mol% relative to diamine in condensation reactions, adjusted for target polymer architecture, viscosity, and radiopacity.

    Downstream process integration

    • Added during thermal step-growth polymerization, in conjunction with standard diamine or diacid chloride monomers, governing molecular weight and distribution of iodine atoms in the chain.

    Final product types

    • High-density polyamide pellets for molding or extrusion
    • Polyimide thin films with identifiable iodine markers
    • Resin intermediates for specialty radiation-resistant components

    4. Precursor for Radiopaque Medical Marker Production

    End-users deploy this specialized acid chloride in the functionalization of micro-marker beads and structured inserts designed for visibility under fluoroscopy or CT. The compound allows localized, high iodine loading in biocompatible matrices required for medical intervention marking.

    Industry compliance standards

    • ISO 10993-5 & 10993-11 (Biological evaluation)
    • 21 CFR 820 QSR (US Medical Devices, where integrated into a device)
    • Ph. Eur. 3.2.2 (Medical device materials composition)

    Typical usage ratio

    • Use level ranges from 2–12 wt% in marker bead compositions, titrated to achieve regulatory minimum radiopacity in final assembly.

    Downstream process integration

    • Grafting onto or doping into functionalized silica or polymer microspheres, followed by stabilization, washing, and sterilization prior to integration into device assemblies.

    Final product types

    • Radiopaque beads for injection or vascular placement
    • Fiducial markers for tumor localization
    • Imaging reference insert modules

    5. Synthesis of Reference Standards and Analytical Probes

    Analytical laboratories and reference material producers utilize 5-Amino-2,4,6-Triiodisophthaloyl Acid Dichloride to synthesize well-defined iodinated calibration compounds and tracer molecules for equipment qualification in radiographic and chromatographic techniques.

    Industry compliance standards

    • ISO 17034:2016 (Reference material producers)
    • ISO/IEC 17025 (Accredited testing laboratories)
    • IUPAC purity requirements for analytical standards

    Typical usage ratio

    • Added precisely in molar equivalent based on stoichiometry required for target compound synthesis; custom-scale, often sub-gram to tens of grams per lot.

    Downstream process integration

    • Used as coupling reagent for site-specific iodination or derivatization, typically under controlled anhydrous conditions, with rigorous intermediate testing for identity and purity at each step.

    Final product types

    • Certified radiographic calibration standards
    • Chromatographic markers for iodine quantitation
    • Analytical grade iodinated tracing agents
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