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Dimethyl 5-Iodoisophthalate

    • Product Name Dimethyl 5-Iodoisophthalate
    • Alias 5-Iodo-1,3-benzenedicarboxylic acid dimethyl ester
    • Einecs 609-187-3
    • 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

    540339

    Productname Dimethyl 5-Iodoisophthalate
    Casnumber 61358-25-6
    Molecularformula C10H9IO4
    Molecularweight 320.08 g/mol
    Appearance White to off-white solid
    Meltingpoint 83-85°C
    Purity Typically ≥98%
    Solubility Slightly soluble in water; soluble in organic solvents such as DMSO, methanol, and acetone
    Boilingpoint No data available (decomposes)
    Density No data available
    Smiles COC(=O)c1cc(I)cc(C(=O)OC)c1
    Inchi InChI=1S/C10H9IO4/c1-14-10(13)7-4-8(11)6-5-9(7)15-2/h4-6H,1-2H3
    Synonyms 5-Iodoisophthalic acid dimethyl ester
    Refractiveindex No data available
    Storagetemperature Store at 2-8°C

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

    Packing & Storage
    Packing Dimethyl 5-Iodoisophthalate is packaged in a 25-gram amber glass bottle with a tamper-evident screw cap and detailed labeling.
    Shipping Dimethyl 5-Iodoisophthalate should be shipped in tightly sealed containers, protected from light and moisture. Handle with appropriate protective equipment and follow relevant hazardous material and international shipping regulations. Label clearly as a chemical substance, and ensure packaging prevents leaks or contamination during transport. Store and ship at room temperature unless specified otherwise.
    Storage Dimethyl 5-Iodoisophthalate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area, away from direct sunlight and incompatible substances such as strong oxidizing agents. Keep the chemical at ambient temperature and protect it from moisture. Ensure storage is secure and clearly labeled, following all local, state, and federal regulations for chemical storage.
    Application of Dimethyl 5-Iodoisophthalate

    Applications of Dimethyl 5-Iodoisophthalate in Industrial Manufacturing

    As a specialized manufacturer of Dimethyl 5-Iodoisophthalate, we consistently supply this unique iodinated aromatic ester to global industrial customers operating at the forefront of advanced materials, pharmaceuticals, and specialty chemicals. Our raw material supports precise downstream formulations under stringent quality and safety requirements. Below, we detail several established and traceable application scenarios, specifying regulatory compliance, technical process details, application-level formulation ratios, and the real end products achieved.

    1. Active Pharmaceutical Ingredient (API) Intermediate Synthesis

    Pharmaceutical manufacturers utilize our material as a halogenated aromatic building block in the synthesis of complex API intermediates, where its iodine atom facilitates selective cross-coupling reactions. This role is critical in high-yield routes for kinase inhibitors and other advanced small molecule drugs under current good manufacturing practices. Downstream chemists value traceability from raw material sourcing through final isolation of intermediates, maintaining batch integrity and regulatory audit readiness throughout the synthesis chain.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • EU GMP Directives for Pharmaceuticals (EudraLex Volume 4)
    • Pharmacopoeia specifications (USP, EP as relevant for APIs in development)
    • FDA 21 CFR Part 211 (as applicable to drug substance intermediates)

    Typical usage ratio

    • Generally 0.1–0.9 molar equivalents relative to principal aromatic starting material; actual dosage tailored based on reaction stoichiometry, desired iodination level, and scale-up studies.

    Downstream process integration

    • Employed during the initial step or first halogenation in multi-step organic synthesis batches; often enters via charge batches under nitrogen, followed by metal-catalyzed coupling or subsequent functionalization. Used prior to key transformation for rapid scale up and downstream purification.

    Final product types

    • N-heterocyclic kinase inhibitor cores
    • Halogenated benzene intermediates for oncology APIs
    • Agrochemical actives for regulated crop protection ingredients
    • Chemical intermediates for late-stage pharmaceutical development

    2. OLED and Electroluminescent Materials Synthesis

    Manufacturers of organic light-emitting diode (OLED) displays and electroluminescent polymers integrate our iodinated aromatic ester into advanced conjugated compounds. The iodo functionality allows introduction of custom substituents via palladium-catalyzed cross-coupling, creating precise molecular scaffolds required for blue-emissive and charge-transport layers in modern display technology. Our product supports these proprietary downstream polymer syntheses under rigorous materials control frameworks.

    Industry compliance standards

    • ISO 9001 for Quality Management in Electronic Materials
    • RoHS (Restriction of Hazardous Substances) compliance—ensured absence of restricted elements in supplied lots
    • REACH registration for import and manufacturing in the EU
    • Customer-specific purity certificates for trace contaminants, especially halogens and heavy metals

    Typical usage ratio

    • Typically 5–20 mole% in respect to the polyaromatic backbone, depending on the electronic properties desired and degree of cross-linking targeted in the monomer synthesis.

    Downstream process integration

    • Fed during Stille or Suzuki-Miyaura coupling stages to install iodinated moieties onto preformed aromatic rings; integrated as a feedstock in pilot-plant scale monomer functionalization prior to polymerization and casting into films or layers.

    Final product types

    • Phosphorescent emitter molecules for OLED pixels
    • Charge-transport organic semiconductors
    • Thin printable films for flexible display substrates
    • Polymeric blue light emitting materials

    3. Specialty Polymer Modifier for High-Performance Engineering Plastics

    Producers of specialty polymers, such as high glass transition copolyesters and flame-retardant polyesters, use our product as a functional modifying group to introduce high molecular weight aromatic iodides. The resulting resins achieve tailored mechanical and thermal profiles suitable for advanced automotive, aerospace, and electronics parts, supporting innovation in durable lightweight materials with enhanced functional group compatibility and downstream resin processing flexibility.

    Industry compliance standards

    • UL 94 Flammability Standard for Plastics
    • ISO 14001 Environmental Management for Production Sites
    • EU REACH compliance for non-food contact polymer additives
    • IEC 61249 for base materials in electrical insulation and PCB lamination (when relevant to end-use)

    Typical usage ratio

    • Ranges from 0.2–3.5 wt% in the target polymer batch; dosage optimized for mechanical impact and flame retardancy while minimizing processing changes in extrusion or injection molding.

    Downstream process integration

    • Added during monomer feed blending ahead of polycondensation reactions; copolymerized or post-modified in reactive extrusion stages, followed by compounding and pelletizing for customer resin specifications.

    Final product types

    • Modified thermoplastic copolyesters (e.g., PET, PBT blends)
    • High strength engineering plastics for automotive connectors
    • Flame-retardant enclosures and housings for electronics
    • Specialty films and sheets for industrial applications

    4. Custom Ligand and Cross-Coupling Intermediate Production

    Producers of custom specialty chemicals and metal complex ligands employ our iodinated phthalate in precision syntheses, where selective halogen-metal exchange or palladium-catalyzed arylation reactions construct multidentate ligands with defined symmetry and reactivity. The material’s consistent iodine content and controlled ester functionality facilitate high-yield, low residual halide synthesis workflows, supporting both research and scale-up production in fine chemical manufacturing.

    Industry compliance standards

    • ISO 9001:2015 for chemical synthesis process control
    • OECD Guidelines for Testing of Chemicals (where applicable for final complexes)
    • Full traceability in accordance with supplier audit protocols of regulated labs
    • SDS and GHS labeling compliance for international transport and handling

    Typical usage ratio

    • Usually 1.0–1.2 molar equivalents when serving as the limiting reagent in ligand precursor assembly; adjusted upward if incomplete halogenation or side-reaction prevention is required at larger scale.

    Downstream process integration

    • Introduced in the initial halogen-substituent introduction step during organometallic synthesis; directly participates in ligand formation followed by deprotection, metal insertion, or additional functionalization prior to final purification and QC analysis.

    Final product types

    • Bidentate and tridentate ligands for catalysis
    • Cross-coupling intermediates for pharmaceuticals and agrochemicals
    • Catalyst precursors for polymer and fine chemical synthesis
    • Electronics-grade organic metal complexes for advanced materials
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    Certification & Compliance
    More Introduction

    Dimethyl 5-Iodoisophthalate: A Chemical Manufacturer’s Perspective

    Proven Performance from Consistent Synthesis

    Over many years of producing Dimethyl 5-Iodoisophthalate, we’ve seen its role as a specialty intermediate truly expand. Our team has refined the process behind this compound—chemical formula C10H9IO4—to respond to the needs of advanced research and industrial synthesis. The core of its appeal lies in its unique structure: two methyl ester groups paired with an iodine atom at the 5-position. This arrangement sets it apart from the usual isophthalates or iodinated aromatics available elsewhere. We consistently aim for a purity above 98 percent, with moisture and trace impurities tightly controlled batch after batch.

    Reliable performance matters far more than publication claims. In actual practice, every small impurity or moisture wrapper can cause project failures, especially in fine chemicals and active pharmaceutical ingredient development. Our protocols around crystallization, filtration, and drying processes set the stage for unmatched reproducibility. Over the years, users have relied on our material when other sources could not deliver consistent melting points, solubility, or reactivity. We take the extra steps—vacuum oven drying, glassware decontamination, minimized light exposure—to protect the integrity of each package. Batch records and sample archives support full traceability.

    The Value of Iodine Placement in Synthesis

    Dimethyl 5-Iodoisophthalate doesn’t simply fill a catalog entry. For synthetic chemists, introducing an iodine atom to the isophthalate skeleton opens a world of reactivity. The 5-position iodide acts as a versatile handle for cross-coupling, Suzuki, Sonogashira, Buchwald–Hartwig, and more. Most suppliers push a low-purity product, which produces erratic coupling yields and sometimes even catalyst poisoning. We understand from our own collaboration with pharma groups that compromised quality can stop a program in its tracks.

    In comparison, non-iodinated isophthalates offer little leverage for further derivatization. Alternatives like dimethyl 2- or 4-iodoisophthalate bring different sterics or electronics, which shift reactivity and selectivity. The 5-iodo variant allows controlled functionalization remote from both methyl esters, giving access to target molecules that would otherwise require multiple protecting-group manipulations. This is why medicinal chemists and materials scientists come to us repeatedly for this specific product, even as other isomers sit on warehouse shelves for months.

    User Feedback in Academic and Commercial Development

    Having worked closely with both academic groups and commercial R&D chemists, we have witnessed real-world outcomes from both successful and unsuccessful projects based on Dimethyl 5-Iodoisophthalate. In pharmaceutical lead development, it often serves as a critical building block for modifying aromatic systems, which enables rapid exploration of structure-activity relationships. Our customers have shared their anecdotal evidence: those using direct halogenated intermediates with unpredictable byproducts end up repeating more experiments and wasting resources. Those committed to material with documented batch backgrounds, like ours, tend to progress discoveries much faster.

    In advanced material science, our customers use this product as a staple in producing custom monomers for specialty polymers, dyes, liquid crystals, and electronic components. The need for a pure, reactive iodine substituent is central for many of these transformations—both at bench scale and in pilot plant settings. The value really lies beyond simple yield; it shows up in consistent polymerization rates, low color generation, and repeatable functionalization.

    The Role of Purity in Downstream Success

    From a manufacturer’s perspective, purity is not about checklist compliance or checkbox marketing. Impurities in iodinated aromatics can include unreacted starting materials, byproduct halides, colored impurities, or traces of acids from work-up. Even residues below one percent will impact downstream hydrogenation or metal-catalyzed processes. Typical traders claim acceptable levels, but the difference is obvious under real conditions—chromatograms drift, melting points broaden, or products decompose. Every time, our advanced purification steps, including repeated recrystallization and controlled-atmosphere handling, ensure the product behaves predictably under demanding conditions.

    In terms of specifications, our Dimethyl 5-Iodoisophthalate consistently delivers a melting point that aligns with accepted literature values and exhibits high miscibility with standard organic solvents, such as dichloromethane, acetonitrile, and dimethylformamide. For applications involving aromatic couplings, a stringent control over residual water and halide ions can make or break long sequences. The difference shows up not in a data sheet—rather, in the lack of unexplained reaction failures.

    Application Highlights from Chemical Manufacturing

    Dimethyl 5-Iodoisophthalate’s specialty status is best illustrated by the breadth of its applications. In one case, a global innovator looking to produce a series of π-conjugated polymers repeatedly experienced batch-to-batch variability from standard suppliers. Transitioning to our material eliminated recurring polymerization irregularities, reducing waste and permitting scale-up beyond the gram-to-multigram range with ease. There’s no replacement for that level of reliability in high-value sectors, be it optoelectronics or medical device coatings.

    In pharmaceutical intermediates, this molecule enables direct access to both electron-rich and electron-deficient derivatives via cross-coupling methodology. Competing esters or chlorides lack this flexibility or introduce alternative side reactions. On several occasions, we’ve helped scale up syntheses for complex heterocycles and ring-fused systems with no loss of activity or purity in the final product—results only possible because the starting material maintained its integrity through the entire batch and across reorders.

    Main Differences from Other Isophthalate Products

    Hydrogen, bromine, or chlorine analogs make up the most widely used isophthalate derivatives. Still, each presents its own challenges. Brominated or chlorinated variants suffer from lower reactivity and higher susceptibility to nucleophilic displacement, narrowing their use in modern, palladium-catalyzed chemistry. The weaker carbon-iodine bond in Dimethyl 5-Iodoisophthalate enables cleaner couplings at milder conditions, favoring functional group tolerance and offering shorter synthetic routes—an enormous benefit both in chiral ligand libraries and advanced material scaffolds.

    Compared to mono-functionalized aromatics, the diester backbone in this molecule opens up access not only to core aromatic transformations but also to downstream ester hydrolysis and amidation. One can build either symmetric or highly functionalized derivatives without tedious multistep protection and deprotection. Our customers regularly note the dropped failure rates in their column purifications when switching from competing non-selective iodinated isomers. This feedback validates our efforts: purity, identity, and structural precision save time on both process scale-up and final compound isolation.

    Supporting Quality through Vertical Integration

    Quality at the source remains the best insurance policy. Our site manages every step, sourcing raw isophthalic acid, carrying out the iodination reaction with freshly distilled reagents, and avoiding stockpiling intermediates that degrade under ambient air or humidity. Each vessel, filter, and storage bin is carefully protected from both trace halides and organics, which cannot be routinely monitored by spot checking but appear later in the form of yellowing, decomposition, or sluggish reactivity.

    We avoid outsourcing or breaking the chain of custody, given the risks uncovered many times over in market audits and customer feedback. These experiences taught us that no outside supplier can offer the same level of transparency or process control—it always pays off in the long run, even amid pressure to reduce costs. Our unbroken batch documentation, reserve sampling, and open-door policy for technical audits have built deep trust, especially from recurring clients engaged in regulated industries.

    Operational Lessons from Decades of Production

    Every chemical manufacturer can recount stories about challenges with specialty iodinated compounds. Early on, we saw how sensitive Dimethyl 5-Iodoisophthalate reacts to even a slight rise in trace water during isolation. We reworked our SOPs, switched to inert-atmosphere handling, and upgraded storage to nitrogen-purged containers. These changes all but eliminated the risk of product deterioration over time, ensuring our customers receive fresh, high-purity material every shipment.

    It’s easy to overlook the pain caused by non-obvious contaminants until a scale-up runs off track or a regulated impurity gets flagged by quality control. We’ve invested in in-house HPLC and NMR analysis for both release and stability checks, which pick up subtle signals that less rigorous screening might miss. Based on this data, we gradually implemented smaller batch sizes for rapid turnaround and fresher material, driven not by marketing but by field experience. Many process chemists have come back to us after encountering unanticipated issues from products sourced via brokers or resellers.

    Packaging Choices to Protect Integrity

    Based on repeated consultation with customers, we updated packaging from industrial fiber drums to smaller amber-glass containers with desiccant and tamper-proof seals. For orders supporting pharmaceutical or electronic applications, single-use packs ensure zero cross-contamination. Small packaging protects from air and light degradation and keeps the material in the condition required for demanding bench work. Over-packing for export shipments keeps temperature and humidity swings within tolerance even during multi-week sea freight.

    While the modification added cost, it prevented nearly all reported problems with clumping, off-coloration, or residue formation seen in previous years. We encouraged feedback and made yearly improvements based directly on chemists’ observations in their own plants and labs. This two-way communication makes a genuine difference in how reliably the product delivers results—especially when research productivity or regulatory compliance depends on reagent consistency.

    Direct Response to Customer Demands and Supply Chain Security

    Supply chain interruptions, especially for iodine and key reagents, showed us how fragile specialty chemical supply can be. We maintain safety stock of starting materials, hedging against market swings and sudden transportation bottlenecks. This helped us remain a trusted partner when others were unable to fill orders on short notice. We’ve invested in backward integration to maintain secure raw material pipelines—never something an opportunistic trader can replicate.

    Major projects often depend on just-in-time delivery of research-grade intermediates. Our approach—direct shipping from production lines to end-user sites, omitting unnecessary warehousing—reduced time-in-transit and ensured product leaves our facility at peak condition. Chemists working on tight timelines have repeatedly acknowledged the difference it makes in project continuity.

    Collaborative Problem-Solving in the Field

    We rarely simply take orders and ship. As a manufacturer, our technical staff have regular exchanges with project teams about reaction optimization, possible byproduct reduction, and the smallest details of purification and storage. Sharing application notes about successful cross-couplings, sidestepping troublesome solubility issues, or minimizing color carryover from bench to pilot scale all goes hand-in-hand with the product itself.

    Our assistance is grounded in actual data and troubleshooting sessions, not marketing gloss. This collaborative attitude extends to handling returns or reclaiming off-spec lots—fewer than two in five hundred shipments require such attention, but each case provides another chance to learn and further upgrade process controls or packaging.

    Supporting Regulatory and Analytical Demands

    Client feedback, particularly from regulated industries, drives continued improvement in our compliance offerings. Each shipment comes with full batch analysis—melting point, NMR, HPLC, and moisture—all titrated to the needs of the application. For GMP-adjacent requirements, we have added impurity profiling, residual solvent analysis, and COA transparency. These measures reflect both laboratory realities and regulatory scrutiny faced by our end users, without adding bureaucracy for its own sake.

    We field frequent technical questions about identity checks—comparing NMR patterns, interpreting endpoint traces, or troubleshooting chromatographic separations. In each case, our internal team provides explanations, application notes, and method validations, based on the unique characteristics of Dimethyl 5-Iodoisophthalate lacking in generic references.

    Building Trust through Real-World Experience

    No amount of advertising or standard documentation equals a direct line to the people actually making the product. Real progress in chemistry depends on shared experience, lessons learned, and iterative problem-solving. Our history refining this compound, year after year, reflects countless discussions, unplanned setbacks, and surprise insights. Maintaining an in-house team of process chemists allows us to translate lessons from the field directly into practice. New customer requirements spur improvements in both synthetic technique and final packaging, with changes implemented in real time rather than through committee or long review cycles.

    Dimethyl 5-Iodoisophthalate earned its niche because it solves problems that less specialized products cannot touch. Over the years, we’ve earned repeat business not only through purity claims or quick quotes but by being present with both technical know-how and transparent communication. Every successful delivery reflects respect for the end user’s challenge as much as for our internal process controls. At the end of the day, the value gained from working directly with a dedicated manufacturer runs deeper than price—the difference becomes clear in total project outcomes and innovation cycles.

    Looking Ahead: Evolving with Research and Industry Needs

    The pace of chemical innovation continues to accelerate, with increasingly complex targets and more demanding methodologies emerging every year. We rethink old approaches, sourcing new reagents or adopting greener, higher-efficiency protocols. Markets for high-performance materials, next-generation pharmaceuticals, and advanced electronics all present challenges that generic intermediates won’t address. Dimethyl 5-Iodoisophthalate stands out by meeting the intersection of reactivity, purity, and adaptability needed for tomorrow’s chemistry.

    By listening to both successes and the rare failures from our customers, we direct resources where they matter most—upgraded synthesis, improved purification, and responsive customer support. The future of specialty iodinated aromatics belongs to those ready to bridge the gap between lab curiosity and commercial reliability. With each shipment, we strengthen that bridge and grow the foundations that innovation stands on.