Iodoacetic Acid

    • Product Name: Iodoacetic Acid
    • Alias: IAA
    • Einecs: 200-717-2
    • Mininmum Order: 1 g
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications

    HS Code

    915862

    Chemical Name Iodoacetic acid
    Synonyms IAA, Iodoethanoic acid
    Molecular Formula C2H3IO2
    Molar Mass 185.95 g/mol
    Appearance White to off-white crystalline powder
    Melting Point 82-86°C
    Solubility In Water Soluble
    Cas Number 64-69-7
    Density 2.27 g/cm³
    Pka 3.18
    Hazard Statements Toxic, may cause irritation
    Storage Conditions Store in a cool, dry place, tightly closed

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

    Packing & Storage
    Packing Iodoacetic Acid, 25g, supplied in a tightly sealed amber glass bottle with hazard labeling and safety information, securely packaged.
    Shipping Iodoacetic acid should be shipped in tightly sealed containers made of compatible materials, clearly labeled, and protected from moisture and light. It must be classified and packaged as a hazardous chemical, following all applicable regulations for toxic and corrosive substances. Transport should be carried out by authorized carriers with appropriate documentation.
    Storage Iodoacetic acid should be stored in a tightly sealed container at room temperature, away from light, moisture, and incompatible substances such as strong bases and oxidizing agents. Store in a well-ventilated, dry area designated for corrosive chemicals. Use secondary containment to prevent spills, and clearly label the container, ensuring access is restricted to trained personnel.
    Application of Iodoacetic Acid

    Purity 98%: Iodoacetic Acid with purity 98% is used in protein sequencing workflows, where it ensures selective alkylation of cysteine residues for accurate peptide mapping.

    Molecular weight 185.94 g/mol: Iodoacetic Acid with molecular weight 185.94 g/mol is used in enzyme inhibition studies, where it provides precise inhibition of cysteine proteases during biochemical assays.

    Melting point 82°C: Iodoacetic Acid with a melting point of 82°C is used in research laboratories, where it maintains compound integrity under moderate temperature conditions for reproducible experimental results.

    Stability temperature 25°C: Iodoacetic Acid with a stability temperature of 25°C is used in reagent storage protocols, where it offers prolonged shelf life and maintains reactivity for laboratory applications.

    Particle size <100 μm: Iodoacetic Acid with particle size less than 100 μm is used in formulation processes, where it ensures homogeneous dispersion of active compound in analytical preparations.

    Solubility in water 10 g/L: Iodoacetic Acid with solubility in water of 10 g/L is used in buffer preparation for biochemical assays, where it enables rapid dissolution and consistent reagent concentration.

    Reagent grade: Iodoacetic Acid of reagent grade is used in electrophoresis sample preparation, where it minimizes contamination risk and ensures high sensitivity in protein detection.

    pH stability range 2-8: Iodoacetic Acid with pH stability range 2-8 is used in diagnostic kit manufacturing, where it maintains chemical effectiveness across various assay conditions.

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    Certification & Compliance
    More Introduction

    Iodoacetic Acid: Precision in Chemical Synthesis

    Introduction to Iodoacetic Acid

    Iodoacetic Acid holds a crucial role in synthetic chemistry and several research-driven applications. As manufacturers, we've witnessed how this compound can alter the pathway of biological and organic reactions, supporting ever-evolving needs in academic and industrial environments. Our experience with Iodoacetic Acid stretches back decades, moving from early lab-scale batches to refined, industrial-level production. We've learned to respect the detail in its physical characteristics and the nuances that separate high purity grades from less refined alternatives.

    The Nature of Iodoacetic Acid

    Iodoacetic Acid is an organoiodine compound with the chemical formula C2H3IO2. With its carboxylic acid group and an iodine atom attached to an acetic acid backbone, this white crystalline powder stands out among simple haloacetic acids. Our process control ensures clarity and consistency in its appearance and reactivity profile, allowing researchers and production teams to count on the same performance, batch after batch.

    In the lab, this molecule acts primarily as an alkylating agent. Its reactivity, stemming from the iodine substituent, is both a benefit and a point to handle with expertise. During manufacturing, we watch carefully for moisture content, trace halides, and color impurities. At typical room temperature, it displays notable stability in sealed packaging, but care during weighing and transfer helps avoid exposure risks—the kind that stem from its inherent chemical strength.

    Specifications That Matter

    Our Iodoacetic Acid consistently achieves a purity above 99%. Every batch undergoes volumetric and chromatographic analysis. Trace levels of bromide or chloride counterions come in well below industry thresholds—often not detected in our final test certificates. Melting ranges (typically 98–101°C) stay tight, giving developers and chemists confidence that their reactions won’t suffer from latent contaminants or variable phase transitions.

    Particle size can influence dissolution and reactivity in different setups. Several colleagues noted over the years that slight batch differences matter for critical protein chemistry. In our practice, sieving and controlled crystallization allow us to tailor granulation as needed, although for most biochemistry and organic applications, a fine, flowable powder proves most practical.

    Experience in Application: Iodoacetic Acid in Biochemistry

    In protein research, Iodoacetic Acid reliably modifies sulfhydryl groups, effectively blocking thiols by carboxymethylation. Many customers, especially those working in electrophoresis and protein sequencing, return to our product for its consistent performance. The acid reacts directly with free cysteine residues, producing a stable, non-reducible derivative that allows large proteins to withstand downstream electrophoresis or mass spectrometry analysis without structural scrambling.

    Some labs favor Iodoacetic Acid over similar alkylating agents because of the milder conditions and clear reaction kinetics. In our own pilot tests, we discovered that buffer selection, pH, and temperature all affect reaction yields—so we advise careful optimization for each experiment. Compared to iodoacetamide, the acid form presents a different solubility profile. Biologists tell us this can simplify purification steps and cut out downstream complications.

    Synthetic Chemistry and Analytical Uses

    In organic synthesis, Iodoacetic Acid unlocks routes to carboxymethylation and other transformations. The iodine atom’s leaving group quality makes it superior for alkylation reactions compared to chloroacetic or bromoacetic acid, especially in cases needing a gentler touch or higher efficiency. Chemists engaged in nucleophilic displacement reactions note the improved yields and fewer byproducts. We’ve also heard from colleagues in analytical chemistry, who rely on Iodoacetic Acid for specialized derivatizations, marking molecules for detection by ultraviolet or mass spectrometry.

    Over time, we compared its performance with bromoacetic and chloroacetic acids side by side. While chloroacetic often appeals for cost reasons, it falls short on reactivity, particularly in harder-to-drive reactions. Substituents and protecting groups can make a world of difference. Iodoacetic Acid, when applied correctly, lets users avoid harsh conditions that would otherwise degrade sensitive reactants.

    Differences from Other Haloacetic Acids

    Our production teams often discuss why Iodoacetic Acid stands apart from other haloacetic acids. The larger, more polarizable iodine atom brings higher reactivity to the molecule. While this requires careful storage and handling—especially to avoid decomposition from improper sealing or direct sunlight—it also brings unique opportunities. Synthetic chemists regularly choose Iodoacetic Acid for challenging alkylations or where side-reactions with chloroacetic or bromoacetic acids are a concern.

    Technical clients sometimes ask about differences in selectivity for biological applications. Through side-by-side in-house experiments, we validated that the acid’s reaction with cysteine proceeds cleaner and with fewer off-target modifications compared to other halogenated acetic acids. The iodide byproduct can be more easily monitored and scavenged, streamlining isolation and cleanup. In our view, the choice hinges on a balance between reactivity, selectivity, and downstream process simplicity.

    Safety and Environmental Considerations

    Years of hands-on manufacturing taught our team that Iodoacetic Acid requires respect for both personal safety and environmental protocols. Our technical crews work in ventilated areas with gloves and face protection. The compound’s toxicity demands thorough training—especially since it can alkylate proteins on skin or mucosal surfaces. We train handling teams to respond quickly in case of spills or accidental contact. Proper storage in tightly sealed, inert containers—away from light and moisture—protects both product quality and worker safety.

    Iodoacetic Acid is not volatile, but accidental release to wastewater or soil can bring hazards to aquatic life. Our facility routes any wash water or filtered particulates through specialized treatment before authorized disposal. Many of our clients express concern for their own lab’s environmental impact. We openly discuss neutralization steps with sodium thiosulfate or other reducing agents that transform the acid’s reactive iodine into harmless iodide ions. Long experience confirms that these practical steps protect both people and downstream ecosystems.

    Packaging and Storage: Practical Observations

    No two chemical facilities maintain exactly the same conditions, so packaging choices matter. Tin-lined or amber glass bottles prove optimal for larger batches, but for frequent or high-volume usage, lined high-density polyethylene containers offer a cost-effective, safe option. We pack in desiccated, inert-atmosphere conditions to guard against hydrolysis or premature degradation. Several years ago, we studied packaging failures and found that even trace exposure to damp conditions triggers color changes and diminishes purity.

    During transport, temperature fluctuations can stress the product and its container. Our logistics teams coordinate with partners for temperature-stable warehousing and rapid delivery to minimize time outside optimal storage. In lengthy projects, repacking into smaller, sealed vials extends shelf life better than repeatedly opening and closing a single large container. These day-to-day lessons feed back into our continuous improvement cycles for product longevity and end-user satisfaction.

    Our Commitment to Integrity and Traceability

    Our entire team operates under a quality mindset that leaves nothing to chance. Each production batch undergoes rigorous in-process checks, from raw iodine and acetic acid feedstocks to the precise additions and reflux conditions at every stage. We retain reference samples and comprehensive data packages for every lot shipped, keeping all records for years beyond industry minimums.

    Some customers requested custom certificate documentation or expanded impurity profiles, and we've invested in advanced chromatography and elemental analysis infrastructure. From handheld FTIR verification to high-resolution mass spec, our labs and operators build confidence in every gram delivered. This attention to detail allows academic labs, pharmaceutical developers, and specialty manufacturers to pursue demanding research with fewer product-induced variables.

    The Role of Technique in Downstream Success

    Every production run tells its own story. Minor fluctuations in source material quality or purification schedules impact the next step in a customer's workflow, whether it’s a critical crosslinking assay or multi-step organic synthesis. Not every manufacturer prioritizes the details behind crystal habit, dusting potential, or bulk density—but we see the difference such factors make in application after application.

    Conversations with experienced users taught us that time saved in purification or troubleshooting often translates into weeks gained on deliverables for complex research projects. Reliable, on-time supply means chemists and biologists focus on results rather than raw material inconsistencies. Our internal testing protocols mimic end-user processes, whether in aqueous buffers for biological alkylation or organic solvents for synthesis, to ensure seamless integration into ongoing research and production.

    Market Demands and Industry Trends

    Research institutions and life science companies require traceable, high-purity materials. Over the years, demand for Iodoacetic Acid has grown as protein analysis and drug discovery fields expanded. Teams working with enzyme inhibitors or site-directed labeling seek single-lot consistency to support reproducible results. We listen closely to these users, seeking ways to boost utility with minimal waste or variability.

    Cost pressures and regulatory changes encourage chemical manufacturers to fine-tune product offerings. As domestic and international regulations on iodine sourcing and chemical purity tighten, we've committed to transparent supply chains. We work with certified suppliers and monitor key intermediates for unexpected byproducts. These behind-the-scenes efforts let our clients navigate compliance hurdles confidently and keep their own product pipelines moving forward.

    Comparisons: Iodoacetic Acid and Similar Reagents

    Chemists sometimes compare Iodoacetic Acid and iodoacetamide. The amide variant tends to be less acidic, dissolving differently and interacting in unique ways with certain proteins. Protein engineers working with sensitive enzymes have pointed out that carboxylic acids, including Iodoacetic Acid, allow easier removal in dialysis or precipitation steps, whereas amides can persist longer in solution and sometimes complicate analysis.

    In synthetic applications, Iodoacetic Acid’s iodine atom offers a better leaving group compared to both chloroacetic and bromoacetic acids, driving faster, more selective reactions. Cost and availability go hand in hand with performance. Iodoacetic Acid carries a higher raw material input price than its lighter halogen cousins, but the value comes in higher yields and fewer problematic side-reactions. We regularly review feedback from pilot trials to balance raw material selection and downstream cost-per-product for our users.

    Responding to Technical Challenges

    Over years working closely with product developers and research chemists, we've become attuned to the hurdles that can arise in alkylation, derivatization, or crosslinking protocols. Solubility in water or buffers can fluctuate slightly with temperature or the presence of certain ions, so our technical support often recommends incremental adjustments. For bioconjugation projects with tight timelines, we can support transition to fresh or specialized packing formats—granular, fine powder, or custom bulk forms—based on results from direct experimental comparisons.

    Some users encounter scale-up challenges moving from small research vials to industrial reactors. Heat management, agitation, and in-line quality control all play larger roles. Our process engineers offer direct consultation on optimizing batch size transitions, based on lab-to-pilot and pilot-to-production experience spanned over several decades. These hands-on insights, earned through real practice, provide value well beyond standard technical data sheets.

    Continuous Improvement: Learning from Collaboration

    Chemistry evolves, and so does our approach to Iodoacetic Acid production. Advances in filtration, crystallization, and impurity capture shifted the baseline for what clients now expect. Our teams attend scientific conferences, visit end-user labs, and host technical webinars to share knowledge and gather feedback. Customer outcomes push us to fine-tune supply chains, production schedules, and quality documentation. Sharing direct results—good or bad—builds partnerships that drive mutual growth, not just transactions.

    A decade ago, most requests centered on basic product supply. Today, clients prefer a collaborative approach, asking for advice on batch documentation, regulatory certifications, and even project-specific stability testing. These broader questions reveal the increasingly complex needs of researchers and manufacturers worldwide. We welcome these conversations and see them as part of our ongoing job in strengthening chemical supply and enabled research.

    Addressing Future Expectations

    The future of Iodoacetic Acid production will demand increased transparency, lower environmental impact, and even tighter quality boundaries. As pressure from environmental regulators and industrial watchdogs grows, our teams already model greener iodine sources and waste treatment systems. Equipment upgrades, process control automation, and expanded traceability all lay groundwork for new expectations in academic and industrial sourcing. We invest strategically so that all downstream users—whether running small-lot biochemistry or ton-scale manufacturing—can depend on reliable, ethical, and responsive supply.

    Looking back over years in this industry, the lessons are clear: close attention to raw material selection, continual investment in people and equipment, and respect for customer outcomes create stronger partnerships and better results. Our daily mission centers on providing Iodoacetic Acid that meets not just a lab spec, but the real-world requirements of every chemist and biologist who relies on it.

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