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Methyl 2-Iodobenzoate

    • Product Name Methyl 2-Iodobenzoate
    • Alias Methyl o-iodobenzoate
    • Einecs 219-273-1
    • 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

    812946

    Cas Number 610-97-9
    Molecular Formula C8H7IO2
    Molecular Weight 262.05 g/mol
    Iupac Name Methyl 2-iodobenzoate
    Appearance White to off-white solid
    Melting Point 40-43 °C
    Boiling Point 291-292 °C
    Density 1.76 g/cm³
    Solubility Slightly soluble in water; soluble in organic solvents
    Smiles COC(=O)C1=CC=CC=C1I
    Inchi InChI=1S/C8H7IO2/c1-11-8(10)6-4-2-3-5-7(6)9/h2-5H,1H3
    Refractive Index 1.61 (estimated)
    Synonyms 2-Iodobenzoic acid methyl ester
    Pubchem Cid 12222

    As an accredited Methyl 2-Iodobenzoate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Methyl 2-Iodobenzoate, 5 grams, is packaged in a sealed amber glass bottle with tamper-evident cap and clear labeling.
    Shipping Methyl 2-Iodobenzoate is shipped in tightly sealed containers, typically amber glass bottles, to protect it from light and moisture. The package is cushioned and labeled according to hazardous material regulations, ensuring safe transport. Shipments comply with international guidelines for chemicals, including UN identification and safety data sheet (SDS) inclusion.
    Storage Methyl 2-iodobenzoate should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from light and incompatible substances, such as strong oxidizing agents. The storage area should be clearly labeled and designed to prevent moisture ingress. Appropriate safety measures, including secondary containment and access restriction to trained personnel, are recommended to ensure safe handling and storage.
    Application of Methyl 2-Iodobenzoate

    Applications of Methyl 2-Iodobenzoate in Industrial Manufacturing

    Methyl 2-Iodobenzoate serves as a specialized intermediate in targeted chemical production. It supports several advanced sectors, notably in pharmaceuticals, crop protection, specialty material synthesis, and dyes. The following application pathways outline its industrial relevance, compliance parameters, technical utilization, and integration into finished goods manufacturing.

    1. Active Pharmaceutical Ingredient Synthesis

    Pharmaceutical manufacturers incorporate Methyl 2-Iodobenzoate primarily as an iodinated building block in multi-stage synthesis routes for several APIs, including anti-inflammatory, antimicrobial, and anticancer agents. Its iodine moiety facilitates electrophilic aromatic substitution and efficient coupling reactions, contributing to rapid scaffold assembly for heterocyclic drug candidates. Regulatory compliance, precise stoichiometric balance, and end-product purity define this application’s requirements throughout all GMP-governed production steps.

    Industry compliance standards

    • ICH Q7 Good Manufacturing Practice for Active Pharmaceutical Ingredients
    • European Pharmacopoeia (Ph. Eur.) monographs
    • US FDA 21 CFR Part 210/211 cGMP Guidelines
    • USP General Chapters

    Typical usage ratio

    • 0.5–1.2 molar equivalents in key coupling steps, adjusted based on substrate reactivity and process scale.

    Downstream process integration

    • Introduced during early to mid-stage steps as a core intermediate; undergoes halogen exchange or substitution followed by subsequent purification before API isolation.

    Final product types

    • Anti-cancer drug precursors
    • Fluoroquinolone derivatives
    • Aryl iodide-containing anti-inflammatory agents
    • Specialty generic API intermediates

    2. Agrochemical Intermediate

    Agrochemical formulators use this molecule in the development of specific herbicide and fungicide actives. Its orthogonal iodination enables targeted benzoate modifications essential for the synthesis of modern crop protection agents. Production lines demand thorough hazard assessment and environmental controls, with batch ratios tailored to seasonal or geographic chemical resistance patterns.

    Industry compliance standards

    • FAO Specification and Evaluation Guidelines
    • REACH Regulation (EC No 1907/2006)
    • ISO 9001:2015 Quality Systems for Agrochemical Manufacturers
    • OECD Principles of Good Laboratory Practice

    Typical usage ratio

    • 5–10% of total intermediate charge per batch; refined through in-process analytical data and efficacy screening.

    Downstream process integration

    • Used in pre-formulation stages as the starting iodobenzoate for further alkylation, oxidation, or coupling toward active agrochemical substances.

    Final product types

    • Pre-emergence herbicide intermediates
    • Fungicide scaffolds for cereals and fruits
    • Leaf-surface protective amides
    • Miticide pre-cursors

    3. Organic Synthesis for Specialty Electronics Chemicals

    Manufacturers in the electronics chemical sector utilize Methyl 2-Iodobenzoate within the synthesis of advanced aromatic compounds for use in photoresist agents, OLED precursors, and semiconductor structuring chemicals. Its electrophilic iodine enables cross-coupling reactions under palladium catalysis, allowing tailored aromatic substitution necessary for high-purity end uses. Process lines closely monitor impurity profiles and batch reproducibility, with strict integration into downstream electronics formulation steps.

    Industry compliance standards

    • SEMI C45 Specification for Electronic Grade Intermediates
    • IATF 16949:2016 for Automotive Electronics Supply Chain
    • RoHS Directive (2011/65/EU)
    • REACH SVHC Reporting

    Typical usage ratio

    • 1–3 mol% as a coupling reagent, depending on target aromatic substitution and final product purity requirements.

    Downstream process integration

    • Feeds into Suzuki-Miyaura and Sonogashira coupling lines to produce high-value substituted benzoates or aryl ethers for electronics-grade resins.

    Final product types

    • OLED intermediate compounds
    • Photoresist resin additives
    • Semiconductor surface treatment intermediates
    • Advanced electronic encapsulation materials

    4. Dyes and Pigments Manufacturing

    Dye and pigment producers rely on Methyl 2-Iodobenzoate in the creation of complex, iodinated aromatic dye intermediates. The presence of the iodine atom increases chromophore reactivity, which is crucial for high-color-strength dispersions and lightfast textile dyes. Manufacturing runs necessitate compliance with environmental discharge limits and require precise dosage to balance yield with cost efficiency.

    Industry compliance standards

    • OEKO-TEX Standard 100
    • ISO 14001 Environmental Management for Dye Manufacturing
    • ZDHC (Zero Discharge of Hazardous Chemicals) MRSL v3.1
    • EU REACH Annex XVII Restrictions (Textiles & Dyes)

    Typical usage ratio

    • 0.8–2.5% w/w in combined aromatic substitution stages, adjusted based on required chromophore intensity.

    Downstream process integration

    • Enters azo coupling or condensation units for creation of intense color intermediates before final dye blending and granulation.

    Final product types

    • Textile reactive dyes
    • Specialty pigment dispersions
    • Inkjet printer dye solutions
    • Paper coating pigments

    5. Fine Chemicals and Laboratory Reagents

    Producers of fine chemicals and specialty reagents use Methyl 2-Iodobenzoate as a reference standard and custom synthesis precursor. Its defined structural reactivity aids in the preparation of labeled standards, calibration materials, and specialty ligands for academic and contract research markets. Production runs focus on controlled scale, trace impurity minimization, and full documentation to meet laboratory QA/QC standards.

    Industry compliance standards

    • ISO/IEC 17025 Laboratory Accreditation
    • ACS Reagent Grade Specifications
    • GHS Labeling per OSHA 29 CFR 1910.1200
    • REACH Registration for Laboratory Use

    Typical usage ratio

    • 0.1–1.0 mmol scale for research; up to 10% of reactant mix in pilot fine chemical campaigns.

    Downstream process integration

    • Dosed directly in small-batch synthesis, with immediate conversion to calibration standards or further derivatization for specialty orders.

    Final product types

    • Chemical analytical standards
    • Reference materials for QC/QA labs
    • Specialized aryl iodide ligands
    • Custom research intermediates
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    Certification & Compliance
    More Introduction

    Methyl 2-Iodobenzoate: Precision for Organic Synthesis

    The Substance at the Core of Modern Research

    At our manufacturing facility, the journey of every kilogram of Methyl 2-Iodobenzoate begins with carefully sourced raw materials. Each batch follows a tightly controlled process that allows us to consistently match analytical expectations for this valuable compound. Methyl 2-Iodobenzoate occupies a vital role in chemistry. Laboratories across the globe use it to build complexity from simplicity, and the way it behaves under a chemist's hands separates reliable work from guesswork.

    Origin, Purpose, and Daily Production Experience

    Methyl 2-Iodobenzoate does not emerge out of thin air. Our team reacts 2-iodobenzoic acid with select methanol grades using catalysis that balances efficiency and purity. Every step involves temperature checks and crystallization control. A faint yellowish solid often appears, which signals the right transition towards our product's isolation. We oxidize, filter, dry, and then pack in containers that block any moisture or unnecessary light. Early days in synthesis required a lot more trial runs, and we spent hours adjusting timings and solvent ratios until results held steady across batches.

    Chemists and industrial users come to us with a common problem: “We need a reliable methyl ester for coupling reactions and further transformation.” They do not want surprise impurities or low yields due to trace contaminants. One routine check we do in-house involves running proton NMR, keeping the methyl doublet and aromatic proton signals sharp and distinct. If a signal falls out of place, it does not leave our site.

    Distinct Features of Our Methyl 2-Iodobenzoate

    The model we supply emerges as the 98%+ pure methyl ester of 2-iodobenzoic acid. Iodine gives it a heavier molecular weight than many related methyl benzoates. This single difference matters for practical chemistry: the C–I bond proves more reactive in cross-coupling reactions, including Suzuki, Sonogashira, and Stille protocols. The reactivity profile allows chemists to achieve biaryl formation, acetylene attachment, or other arylations with milder conditions compared to bromo- or chloro- derivatives.

    During annual reviews, partners point out that our material dissolves smoothly in common organic solvents like DCM and THF. That sounds routine until a project demands precise stoichiometry at low concentrations. Low solubility can throw off the timing in dropwise additions or create clouding in reactions that involve catalysts. Through regular QC feedback, our approach favors crystallization steps that clean out side-by-products, which would otherwise become stubborn oils or sticky residues.

    Some resellers mix lots or supplement their stock with less stringent material. Operating as the producer, we have the advantage: every label, tracking code, and certificate links straight back to our original run data and raw inventory. This accountability means if someone raises a batch quality question, we resolve it in days, not weeks. Many clients appreciate that peace of mind. They do not want to risk an interrupted synthesis because of a missing spec.

    Practical Applications in Academic and Industrial Synthesis

    Users rely on Methyl 2-Iodobenzoate for carbon-carbon bond formation, especially in building blocks for pharmaceuticals, materials science, and agrochemical research. The methyl ester serves as a masked carboxylic acid, staying intact until later stages. Iodine makes site-selective activation possible, so downstream processes can fine-tune substitution patterns or release the methyl group under gentle saponification. Lab teams value that flexibility, especially when designing synthetic routes to minimize steps and reduce unnecessary protection/deprotection cycles.

    Researchers in medicinal chemistry reach for our product to link aromatic rings, push into new chemical space, or introduce small changes at specific points on a molecule. Scale-up groups in pilot plants approach things differently; they want kilogram lots with identical behavior to what they used on a gram scale.

    Compared to methyl 2-bromobenzoate or methyl 2-chlorobenzoate, the iodine analog offers lower activation barriers in transition-metal catalyzed transformations. That translates into shorter reaction times and higher yields, which lets process engineers save energy and costs. Over time, feedback from end-users led us to optimize our washing and recrystallization cycle to avoid issues found with brine residues or micro-particles that clog filters.

    Handling, Storage, and Transport Experience

    On arrival, Methyl 2-Iodobenzoate presents as pale yellow crystals, sometimes with a faint sweet odor typical of esters. Storage involves keeping material in a dry, dark spot below 30°C. Humidity or bright light slowly degrades the ester, shortening shelf life and darkening the compound. Shipping overseas, we double-seal drums with liners to avoid exposure in transit. Inside our own warehouse, rotating stock and regular visual checks help us pick the oldest lot for each order. We want partners to work with fresh product, not leftovers sitting too long.

    The physical properties—melting point, density, boiling point—match published standards. Each shipment leaves with up-to-date analysis, including GC purity, water content by Karl Fischer, and trace metal analysis. Customers sometimes care as much about elemental halogen content as about organics, since some downstream catalysts can deactivate in the presence of impurities. Detailed feedback reports from frequent partners drive our improvements in product handling and shipment.

    Why Choose Our Material Over Other Options

    Production scale influences cost. Large producers like us control every step, which lets us batch-wise test and scale up or down as project needs evolve. That beats piecemeal purchases from anonymous traders, especially if a project changes direction. Local partners often tell us it’s the follow-through that sets a real manufacturer apart: they receive shipment on the timeline we promise, and every question about batch data has a precise answer.

    Some chemical suppliers offer cheaper variants with visible by-products or noticeable off-odors. Often, these products have unreacted acid or excess methylating agents, which users discover far into their workflow. Our approach focuses on avoiding runner-up material. Instead, up-front investment in purification chops off 90% of synthesis headaches down the line.

    Working with kilo-lot buyers, we learned that switching to our material reduced scaling problems, cutting loss during work-up, and improving filtration rates. In trials with academic partners, early switching from a lab-made batch to our large-scale product cut the number of dropped reactions, allowing more consistent reporting of results for publication.

    Supporting Innovation: Examples from the Field

    In fields like medicinal chemistry, one senior chemist reached out to report that the combination of our Methyl 2-Iodobenzoate and a proprietary palladium catalyst cut their reaction times in half compared to previous material. The result was fewer overnight runs and a more predictable workflow for the entire team. Another client, running a continuous flow process, saw meaningfully improved pumpability and fewer blockages in their transfer lines. These practical outcomes only come from material that ships at the right spec, not from paper descriptions.

    Our technical staff collaborates with academic groups developing novel cross-coupling ligands. Early access to clean Methyl 2-Iodobenzoate lets them focus on chemistry rather than waste time de-gumming or filtering subpar material. At pilot scale, process engineers point to smoother column purification owing to the absence of polymeric by-products. Smoother purification saves time and solvent, and often spells the difference between a pilot batch and a publishable one.

    Some contract manufacturers explained how impurity-free feeds improve downstream hydrogenation steps. With tightly controlled iodine levels and clean spectra, the catalyst life extended batch after batch—something that reduces cost and downtime for both upstream and downstream steps.

    Challenges and Solutions from a Manufacturer’s Perspective

    Manufacturing isn’t just mixing and pouring. In Methyl 2-Iodobenzoate, exothermic stages demand careful monitoring. We record every temperature shift and agitation rate, using thermal imaging to spot inconsistency before it causes problems. Small errors lead to darker product and unwanted side-products. In the early years, we lost entire lots from missing that margin. Now, layered control systems and well-trained operators keep every batch consistent.

    Unwanted water is a recurring challenge. Even low levels of moisture lead to hydrolysis and trace acid formation. We battle humidity at every transfer and switch gloves between steps. Leakage in reagent storage or unreplaced desiccants invite contamination. We worked through procedures for dry transfer and added dew point monitoring to critical rooms. Over time, this cut hydrolysis complaints to almost zero.

    Handling strong acids and halogen reagents means working with risk assessments, PPE, and redundant ventilation. Front-line staff join frequent safety reviews. No matter how many batches precede, every run relies on checklists and peer-crosschecks. This minimizes accidental loss and maintains staff safety, all while preventing surprise shutdowns.

    Local regulations for waste iodine or spent solvent disposal push for ever-better capture and recovery rates. We invested in on-site solvent recycling and run dedicated waste neutralization units for halogenated streams, reducing both our environmental footprint and the probability of off-spec by-products leaving our plant. Downstream, our partners report better results when these residues stay out of their own waste.

    Market and Supply Trends: How Scale Shapes the Product

    Stable global demand for cross-coupling building blocks keeps us vigilant on sourcing and logistics. Raw iodine supply sometimes varies due to regulation or upstream mining interruptions, especially in certain regions. Years ago, price swings interrupted production runs. To overcome this, we built a distributed sourcing plan, drawing from several vetted iodine suppliers scattered across geographies. Local partners help monitor logistics in real-time, adjusting shipments before issues turn critical.

    The market now expects more traceability and compliance with new green chemistry initiatives. Requests for solvent-recovery rates, water-use data, and LC/MS testing arrive every season. Internally, we log batch data on a secure platform, accessible remotely by our analysts. This allows real-time optimization and trace-level impurity mapping. We see a growing expectation among large customers for not just high-purity raw material, but for supporting documentation that tracks every handoff and process variable from start to finish.

    Comparing to Related Compounds

    The switch from bromo or chloro analogs makes sense to synthetic chemists because Methyl 2-Iodobenzoate reacts at lower temperatures and requires less forcing conditions. That translates into cost-saving through milder bases, less aggressive heating, and improved compatibility with sensitive functional groups. Our commitment after several years in production includes confirming that this material works in parallel to the most demanding reactions—ones that fail with inferior aryl halides.

    We avoid generic statements about “fits all” or “tailored” product differentiation. Instead, side-by-side pilot studies run by well-known laboratories show that our batches perform at or above reported literature yields. Teams have shared reaction times and isolated yields comparing a single variable—the source ester—revealing higher reproducibility and fewer outlier failures from our material.

    Technical Support and the Value of Direct Manufacturer Relationships

    Questions do not sit unanswered here. Our technical support staff fields inquiries daily about solubility, compatibility with emerging catalyst systems, and batch-to-batch analysis. Having in-house chemists who know the synthesis and purification means we sort real questions from theoretical ones fast. Once a partner shipped back a drum they suspected of cross-contamination. Running comparative analysis, we pinpointed a rare handling issue at their facility, and our insight let them correct course before more valuable intermediates went to waste.

    Building trust is a slow, cumulative process. Researchers, process engineers, and procurement leads contact the manufacturer directly for updates on lead times or special grade orders. Every year, partners come back with new project-specific demands, such as tighter control on alkali residue or specific limits on trace metals. Instead of passing the request down a chain, we walk it back through our lab and adjust the process accordingly. Being the maker, not the middleman, means complete control over the end product and the ability to respond flexibly and quickly.

    Future Outlook: Sustainable Manufacturing and Innovation

    The push for sustainability won’t wait. Modern labs care about carbon footprint and upstream transparency as much as price and quality. Years ago, few asked for lifecycle data on intermediates. Now, every major order brings requests for energy use stats and alternative solvent approaches. We re-engineered our workflow, shifting from purely petroleum-derived solvents to greener options where possible. Continuous feedback improves how we reclaim waste and avoid off-gas emissions in halogen handling.

    Regulatory shifts impact manufacturing choices daily. As more regions adopt stricter control measures on aryl iodides and related precursors, our compliance team updates documentation and verifies every export matches destination-country expectations. Partners count on us not only to meet immediate analytical needs but to keep their projects moving past regulatory bottlenecks.

    Ambition in research drives demand for higher-purity, specialty grades. We field bespoke requests for low-metal, ultra-low halogen, or high-optical purity variants of common intermediates. Our pipeline includes updated filtration and chromatography processes adapted from pharmaceutical best practices. These investments pay off in client retention and in the steady reputation for reliability and performance.

    Final Thoughts from the Manufacturer

    Long-term relationships depend on more than spot pricing or generic assurance. We learn from every complaint and every successful large-scale run using our Methyl 2-Iodobenzoate. It's these granular lessons that shape each improvement, keeping our material at the level required by top research and commercial teams. More than a label or a spec sheet, it’s the collective labor of process chemists, QA managers, technical support, and logistics coordinators that delivers material ready for the most demanding transformations.

    Anyone can distribute chemicals, but only those who control and improve their process at every step make a long-term difference in research and manufacturing progress. Methyl 2-Iodobenzoate is more than a reagent—it’s our pledge that chemistry at the frontline meets tomorrow’s ambitions and stays grounded in the reliability users deserve.