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Iodoacetic Acid

    • Product Name Iodoacetic Acid
    • Alias IAA
    • Einecs 201-198-7
    • 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

    590210

    CAS_Number 64-69-7
    Molecular_Formula C2H3IO2
    Molecular_Weight 185.95 g/mol
    Appearance White crystalline solid
    Melting_Point 97-100 °C
    Boiling_Point 255 °C (decomposes)
    Solubility_in_Water Very soluble
    pH 1.5 (10 g/L at 20°C)
    Density 2.29 g/cm³
    Odor Slightly pungent

    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 is supplied in a 100g amber glass bottle, with a tightly sealed cap and safety labeling in accordance with hazardous materials regulations.
    Shipping Iodoacetic Acid should be shipped in tightly sealed containers, protected from light and moisture, in compliance with hazardous chemical regulations. Handle as a toxic substance—avoid exposure, and label clearly as dangerous goods. During transport, use appropriate UN packaging and documentation. Recommended shipping temperature is ambient, but avoid extreme heat or freezing.
    Storage Iodoacetic acid should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and moisture. Keep it tightly sealed in a corrosive-resistant container and segregate from incompatible substances such as strong bases and oxidizing agents. Ensure proper labeling and store in a chemical storage cabinet, following institutional safety guidelines and local regulatory requirements for hazardous chemicals.
    Application of Iodoacetic Acid

    Applications of Iodoacetic Acid in Industrial Manufacturing

    Iodoacetic Acid plays a critical role in several specialized industrial sectors, each requiring stringent compliance with industry guidelines and carefully controlled formulation procedures. As a direct manufacturer, we support downstream users with consistent quality and technical expertise to ensure reliable performance in distinct applications, from biochemical manufacturing to nucleic acid research and pharmaceutical synthesis.

    1. Enzyme Inactivation Reagent for Protein Analysis

    Researchers and contract manufacturers use iodoacetic acid as a reliable sulfhydryl-blocking agent to irreversibly inhibit cysteine residues during protein structural and enzymatic studies. This function is essential for accurate mapping of disulfide bonds and controlling enzymatic activity during protein isolation and proteomics workflows, contributing to reproducible data and ensuring that downstream assays remain uncontaminated by proteolytic degradation.

    Industry compliance standards

    • ISO 9001:2015 Quality Management Systems
    • Good Laboratory Practice (GLP)
    • OECD Guidelines for the Testing of Chemicals
    • FDA 21 CFR Part 211 (pharmaceutical testing)

    Typical usage ratio

    • 0.1 mM to 10 mM in buffer, adjusted based on protein concentration and volume
    • Higher levels may be required for complex mixtures or large-scale batch processing

    Downstream process integration

    • Added post-cell lysis or following initial protein extraction
    • Applied prior to electrophoresis, chromatography, or further protein digestion steps

    Final product types

    • Protein reference standards
    • Enzyme assay kits
    • Proteomics analysis panels
    • Therapeutic protein formulations under research

    2. Synthesis Intermediate for Nucleic Acid Crosslinking Agents

    Manufacturers of molecular biology reagents utilize iodoacetic acid as an alkylating intermediate in the production of compounds designed to crosslink or modify nucleic acids. Its role is specific in preparing activated intermediates for applications in mutagenesis, labeling, and nucleic acid interaction inhibitors, contributing directly to the controlled chemical modification of DNA and RNA during assay or kit formulation.

    Industry compliance standards

    • ISO 13485:2016 (Medical Devices & IVDs)
    • REACH Regulation (EC) No 1907/2006 for chemical safety
    • European Pharmacopoeia 10.0 (for nucleic acid reagents)

    Typical usage ratio

    • 0.5 to 5% w/w relative to other reactants, optimized based on desired crosslinking efficiency
    • Lower end for analytical labeling; higher for functional crosslinkers

    Downstream process integration

    • Introduced during reaction step for nucleic acid derivative synthesis
    • Careful stoichiometric calculation to ensure precise molecular modification

    Final product types

    • DNA crosslinking reagents
    • RNA labeling kits
    • Nucleic acid modification chemicals for molecular biology
    • Site-directed mutagenesis tools

    3. Pharmaceutical API Synthesis: Carboxymethylated Intermediates

    Iodoacetic acid remains essential for producing carboxymethylated pharmaceutical intermediates via nucleophilic substitution, especially in small-molecule API synthesis where controlled introduction of carboxymethyl groups determines the final molecule's pharmacokinetic profile. Pharmaceutical manufacturers require tightly controlled reaction conditions to meet regulatory expectations regarding purity, yield, and traceability throughout multi-stage API synthesis campaigns.

    Industry compliance standards

    • cGMP (Current Good Manufacturing Practice, ICH Q7 guidelines)
    • USP General Chapters & Monographs
    • ICH Q3A/B for impurity profiling
    • Ph. Eur. standards for synthetic drug substances

    Typical usage ratio

    • Stoichiometric to slight excess (1.1–1.3 equivalents), dependent on substrate reactivity
    • Adjusted according to stepwise yield optimization and impurity minimization

    Downstream process integration

    • Charged in solution-phase synthesis during alkylation or acylation steps
    • Serves as a key agent in late-stage or side-chain modification reactions

    Final product types

    • Active pharmaceutical ingredient intermediates
    • Specialty drug building blocks
    • Modified amino acids for peptide drug development
    • Carboxymethylated drug precursors

    4. Biochemical Reagent for Enzyme Kinetics and Mechanism Studies

    Specialty reagent suppliers and industrial laboratories deploy iodoacetic acid to probe active site function in dehydrogenases, kinases, and thiol-dependent enzymes. By selectively blocking cysteine sulfhydryl groups, it enables mechanistic research into catalytic pathways, transition state stabilization, and enzyme inhibition—key considerations for both academic studies and the design of targeted inhibitors in drug discovery workflows.

    Industry compliance standards

    • GLP Certification
    • OECD 407 Guideline for repeated dose toxicity studies (test systems)
    • ISO/IEC 17025:2017 (Testing and calibration laboratories)

    Typical usage ratio

    • 10 μM to 5 mM, titrated to complete thiol inactivation while minimizing off-target modification
    • Optimized for individual enzyme assay composition and substrate concentration

    Downstream process integration

    • Added after initial enzyme isolation or just before kinetic measurements
    • Included in enzyme-substrate reaction mixtures for mechanistic perturbation

    Final product types

    • Enzyme activity assay reagents
    • Biochemical research kits
    • Mechanism of action screening panels
    • Enzyme inhibition profiling tools

    5. Specialty Synthesis for Modification of Amino Acids and Peptides

    Custom synthesis enterprises rely on iodoacetic acid for the targeted carboxymethylation of cysteine in peptides and amino acids, rendering them unreactive for subsequent bioconjugation stages. This transformation underpins the design of modified peptides for peptide mapping, pharmaceutical probes, and protein immobilization technologies, demanding high purity and consistent performance in multi-step solid-phase and solution-phase syntheses.

    Industry compliance standards

    • ISO 9001:2015
    • ICH Q11 for drug substance manufacturing
    • USP & Ph. Eur. for amino acid/peptide reference materials

    Typical usage ratio

    • 1–2 molar equivalents relative to cysteine content
    • Fine-tuned to minimize overalkylation in complex peptide mixtures

    Downstream process integration

    • Employed during or immediately after selective cysteine deprotection
    • Integrated into solid-phase peptide synthesis (SPPS) or solution-phase protocols

    Final product types

    • Carboxymethyl-cysteine peptides
    • Peptide mapping standards
    • Modified peptide probes for analytical chemistry
    • Chemically stabilized peptide APIs and research reagents
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    Certification & Compliance
    More Introduction

    Iodoacetic Acid: A Closer Look from a Manufacturing Perspective

    Understanding Iodoacetic Acid in Practical Terms

    In the world of specialty chemicals, iodoacetic acid stands out for its solid track record and practical function in both research and industry. At our plant, we have spent years refining the process to yield a product that matches the consistent demands of life sciences, synthesis, and sometimes even niche pharmaceutical applications. The chemistry behind iodoacetic acid—formulated as C2H3IO2—has drawn attention not only for its analytical reliability but also for its reactivity, which facilitates specific modifications in biomolecules. The product is often delivered in its pure crystalline form, a solid white powder, and is priced by quality grades, ranging from laboratory-use purity to more highly refined material for industrial synthesis.

    Manufacturing iodoacetic acid comes with its own set of challenges. We rely on precise controls during halogenation and careful monitoring of temperature, as this can overtly affect product purity. Specifications typically include a purity content above 98%, matching what researchers require to ensure consistent performance in sensitive applications like enzyme inhibition or as an alkylating agent in proteomics studies. For reference, our standard production batches undergo GC, HPLC, and NMR verification. Ensuring rigorous analytical testing, we grant full disclosure of the methods used for those who need traceability—this aligns with the expectations of universities, biotech manufacturers, and QA professionals.

    Iodoacetic Acid Versus Other Alkylating Agents

    Having worked extensively with both iodoacetic acid and other carboxylic acid derivatives such as chloroacetic acid and bromoacetic acid, the differences become plain not only in reactivity but also in application scope. The iodo- substituent, more reactive toward nucleophiles than its chloro or bromo counterparts, enables more efficient alkylation of thiol groups in proteins. In practical terms, this means fewer side products and faster reaction rates in biochemical experiments requiring covalent protein labeling, especially during the preparation of protein standards or in studies seeking to block enzymatic activity at cysteine residues.

    Chemically, the iodine group’s size and electron-withdrawing effect outpace both chlorine and bromine analogues, driving the product to act more aggressively in nucleophilic substitution reactions. This difference shows up most where precision and reaction time matter, such as in mass spectrometry sample preparation or protein crystallography. On the flip side, the higher reactivity commands respect: improper handling can lead to side reactions and waste. Our experience has taught us that clear, practical instructions on storage and handling—cool, dry, airtight conditions—do more for customer satisfaction than generic statements about “shelf life.”

    Practical Application and Stories from the Floor

    In the early years, a major hurdle involved maintaining stable batches while eliminating trace contaminants that could skew experimental results. Based on direct feedback from analytical chemists, we shifted to smaller, more tightly controlled batch sizes. The switch dramatically cut down on batch-to-batch variability. Our QC team sometimes spends more time troubleshooting impurities—like residual iodine or acetic acid—than on the actual synthesis itself. Such extra steps add to the cost, but we realized customers notice purity fluctuations long before price differences.

    Once, a run of iodoacetic acid generated a slightly yellowish powder, which did not match our standard. We traced the issue to oxygen exposure during drying. Rectifying the airflow and adding a final, inert-gas flush solved the problem. This hands-on experience highlights why manufacturing perspectives matter—there’s a direct line from the production floor to the research bench, and even a detail as small as final drying conditions can ripple through to affect experimental outcomes.

    Feedback loops with biochemists taught us that labeling—simply calling the product “Iodoacetic Acid, 99% min”—is not enough. They wanted to see not just assay results, but also detailed impurity profiles and clear records of the analytical techniques used. Adopting transparent reporting and offering small batch certificates has turned occasional buyers into regular partners, because trust in our processes translates directly to trust in their research.

    Why Purity and Traceability Hold Value for Research and Industry

    From the manufacturer’s side, providing high-purity iodoacetic acid is not just about hitting technical targets. The biotechnological landscape demands full traceability—labs conducting proteomic or enzymatic studies need every lot to stand up to regulatory scrutiny and reproducibility standards. Lot-to-lot consistency supports peer-reviewed publications, patent applications, and entire pipelines for drug discovery or protein sequencing. Mistakes or variability carry costs, not just in dollars, but in wasted time, failed experiments, or even delayed launches for biotech firms. That’s motivation enough for us to invest in robust analytical infrastructure and steady employee training.

    Some years ago, a university-driven structural genomics project reached out about unexplained results in a long-running protein analysis series. Our review of archived batch records, including specific chromatography data and even technician shift notes, helped them track down a source of interference—a trace halogen impurity unique to just one lot. Their ability to retrieve data quickly and align it with their own analytical records underscored the value of transparent documentation. These experiences reinforce our focus on complete traceability and rigorous archiving.

    Efficiency on the Production Line: Health, Safety, and Environmental Commitments

    Handling iodoacetic acid raw materials exposes production staff to potent alkylating agents. Over the years, we have developed protocols that minimize risk yet maintain efficiency. We never cut corners by under-ventilating or reducing PPE standards—even if the process takes longer. Air monitoring, spill containment, and proper disposal procedures come from hard lessons and ongoing risk assessments. We stay attentive to regulatory frameworks and periodically invite outside specialists to review our workplace practices.

    Minimizing waste translates to direct savings. Each batch is carefully weighed and tracked. Missteps that lead to spills or unaccounted-for residues result in paperwork and reprocessing, neither of which help our bottom line. Improving waste reduction often involves simple, low-cost changes: revised decanting techniques, improved seals on storage vessels, and regular calibration of dispensing equipment. These efforts don’t just benefit the environment; they enhance morale on the line when staff see management taking seriously the commitments to safety and sustainability.

    Applications and Trends: From Bench to Industry

    In the market, we see iodoacetic acid in small-volume, high-value streams. Its predominant use in inhibiting enzyme activity during protein isolation, especially in proteomics or mass spectrometry studies, creates demand cycles that are closely linked to research budgets and academic trends. Instruments and protocols change rapidly in this sector, so we try to stay close to our core user base via surveys and direct technical support. This hands-on approach gives us advance warning about shifts, like the move from radioactive to stable isotope-labeled samples, which change both purity requirements and supporting documentation needs.

    Beyond life sciences, the compound’s role as a synthetic intermediate in fine chemical manufacturing has created periodic spikes in demand. On occasion, inquiries have arrived for specialty uses in diagnostics or in the synthesis of contrast agents for imaging technology. These projects typically require unique specification adjustments—sometimes finer granulation, sometimes custom blending or solvent-free formulations. We maintain flexibility in batch sizing to accommodate both routine and one-off custom runs without compromising on process verification.

    Complexities in Global Supply, and Responding to Regulatory Pressures

    The regulatory environment defines the operating reality for chemical manufacturers. REACH and other international frameworks put constraints on both raw material sourcing and final product transport. Certifications for shipment across borders often hinge on minute documentation differences or the ability to verify the removal of trace contaminants. Keeping up means ongoing investment in compliance training, legal reviews, and logistics support.

    A few seasons ago, tighter controls on halogenated compounds changed the timing and costs for a series of product exports. Delay in any compliance paperwork can strand product on the dock, potentially spoiling weeks of work and frustrating committed customers. We responded by automating much of the compliance documentation and having live technical staff review each lot file before it leaves our site—no paperwork, no shipment. This policy sometimes creates short-term bottlenecks, but it pays off in long-term credibility with customs and clients alike.

    Newer environmental regulations require us to track the lifecycle of not just our products but all inputs, down to solvents and process aids. Our ongoing move toward “greener” production pathways involves substituting lower-toxicity solvents and scaling down batch emissions. Each modification means more work for development and quality assurance, but the risk of non-compliance is simply too high to ignore. We find that staying ahead of these requirements, even by a few months, prevents disruption and surprises down the line.

    Market Realities: Challenges in Pricing and Availability

    Cost pressures for specialty reagents like iodoacetic acid rarely ease. Raw iodine and acetic acid both fluctuate in price according to global commodity trends, geopolitical issues, and supply chain disruptions. We hedge risks by keeping robust inventory and fostering long-term supplier relationships. Nonetheless, shortages or spikes can affect both our pricing and the timelines we offer downstream. Rather than mask these realities, we prioritize honesty with partners, providing early warnings if deliveries might fall behind and working together on contingency plans.

    In some instances, market shortages have driven customers toward lower-grade sources or unauthorized resellers. The knock-on effects on performance and product safety are real: we have seen cases where poorly characterized or substandard batches led to failed analyses, useless results, and even financial loss when projects had to be restarted. As a manufacturer, we stick to our quality benchmarks, resisting the temptation to cut corners or dilute standards simply to save on cost or time. This stance builds partnerships built on mutual trust and technical respect, which is worth more than a fleeting price advantage.

    Knowledge Gained from Manufacturing Experience

    Producing iodoacetic acid connects chemistry, engineering, quality assurance, and end-user needs in a way that few specialty chemicals do. Continuous improvement is a daily reality, whether tuning crystallization settings, designing more robust packaging, or developing improved analytical protocols for fast turnaround. Years of running batch reactors reveal that walking the floor, talking with operators, and listening to what isn’t working in real time delivers more improvement than any amount of theoretical planning.

    We hold regular review sessions for both successes and mistakes. Operators offer the first warning about a subtle shift in odor, color, or crystallite structure—signs that a parameter has drifted and could impact the final product. Acting swiftly, with clear communication across teams, has prevented full batch losses more than once. Rather than relying solely on final specs, we embed quality checks into each step of the process. Not only do we record every stage, but we also encourage everyone on the team to flag even minor concerns—no hierarchy, no hesitation.

    Final Thoughts: Looking Ahead with Both Tradition and Innovation

    Manufacturing iodoacetic acid has never been a “set and forget” proposition. The compound’s role in rapidly changing fields means we keep one foot in the established processes that assure batch-to-batch reliability, and one eye on new regulation, customer needs, and competitive pressures. Relationships with end users—whether leading biomedical research centers or innovative industrial startups—are built on steady, clear technical support and a willingness to troubleshoot jointly in challenging situations.

    The tools of the trade, from HPLC to mass spec to batch control charts, are only as effective as the people who wield them. We invest in ongoing technical education and back open-door policies for internal discussion. Patterns emerge in customer feedback, and we use those observations to guide both process upgrades and client outreach.

    In sum, iodoacetic acid stands as more than just another carboxylic acid derivative. From a manufacturing perspective, the route from raw material sourcing through final shipment is a complex, sometimes unpredictable process—one best managed by equal parts experience, transparency, and steady teamwork. The best reward: seeing our work advance scientific discovery or industrial innovation, knowing the product’s reliability rested on choices made day in and day out, on the floor and in the lab.