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HS Code |
491368 |
| ChemicalName | Ethyl Iodoacetate |
| CASNumber | 623-48-3 |
| MolecularFormula | C4H7IO2 |
| MolarMass | 214.00 g/mol |
| Appearance | Clear to pale yellow liquid |
| BoilingPoint | 155-158 °C (at 760 mmHg) |
| MeltingPoint | -30 °C |
| Density | 1.773 g/mL at 25 °C |
| RefractiveIndex | 1.512 |
| Solubility | Insoluble in water; soluble in organic solvents |
| FlashPoint | 60 °C (closed cup) |
| StorageTemperature | 2-8 °C |
| Synonyms | Iodoacetic acid ethyl ester |
| SMILES | CCOC(=O)CI |
| ECNumber | 210-792-0 |
As an accredited Ethyl Iodoacetate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Ethyl Iodoacetate, 100g, is packaged in an amber glass bottle with a secure screw cap, labeled with hazard and handling information. |
| Shipping | Ethyl Iodoacetate should be shipped in tightly sealed containers, protected from light and moisture, and clearly labeled as hazardous. It must be packed in accordance with local, national, and international regulations for hazardous chemicals, typically as a Class 6.1 toxic substance. Shipment should be via approved carriers with proper documentation. |
| Storage | **Ethyl Iodoacetate** should be stored in a tightly closed container, away from light, moisture, and incompatible substances such as strong oxidizers, acids, and bases. Keep it in a cool, dry, and well-ventilated area, preferably in a flammable chemicals cabinet. Ensure secondary containment to prevent leaks and label the storage area clearly to indicate hazardous and potentially toxic properties. |
Applications of Ethyl Iodoacetate in Industrial ManufacturingEthyl iodoacetate serves as a purpose-built intermediate across select industrial sectors where its unique iodoalkyl ester functionality drives targeted synthesis steps. Our direct manufacturing control ensures reliable supply, process homogeneity, and batch reproducibility for sophisticated downstream formulations. Below we detail principal use segments recognized by regulatory, pharmaceutical, and chemical industries. 1. Pharmaceutical Active Ingredient SynthesisPharmaceutical manufacturers rely on ethyl iodoacetate as a specialized alkylating agent when preparing key intermediates for active pharmaceutical ingredients (APIs), particularly within β-lactam antibiotic, peptide inhibitor, and CNS drug synthesis. Its reagent role is defined in chiral amino acid derivatization, S-alkylation of cysteine residues, and as a precursor in constructing heterocyclic scaffolds. Downstream QC must track for residuals according to global pharmacopoeial limits, and validated process steps ensure precise incorporation without cross-contamination in multi-purpose plants. Process engineers calculate exact charge rates based on target conversion yields and batch-scale run parameters, ensuring reaction safety and yield consistency. Industry compliance standards
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2. Peptide & Protein ModificationBiotechnology and peptide synthesis facilities use ethyl iodoacetate in solid-phase and solution-phase modification of thiol-containing peptides and protein fragments. The material enables stable S-carboxyethyl adducts, allowing for site-selective immobilization, crosslinking, or functionalization even under controlled GMP conditions. Stringent QC testing and validated cleaning protocols are required to eliminate carry-over and ensure traceability in high-purity biological products. Industry compliance standards
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3. Agrochemical Intermediate ProductionAgrochemical synthesis plants employ ethyl iodoacetate as a specialized alkylation intermediate for constructing insecticide and fungicide molecules. Adoption fits strictly within facilities designed for halogenated precursor handling, with solvent, temperature, and reaction containment regimes specified by chemical safety regulations. Custom formulation teams monitor the residual ester and in-process impurities to maintain compliance with international regulatory submissions. Industry compliance standards
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4. Fine Chemical and Research Reagent ManufacturingProducers of analytical reagents and fine chemicals incorporate ethyl iodoacetate in catalog reagent lines and customized building block packages for both academic and industrial research. The compound features in selective methylation or carboxyethylation of analytes, as well as in advanced organic synthesis studies where precise functional group transfer is necessary. Packaging, storage, and labeling meet laboratory hazardous material regulations, with handling protocols aimed at stability preservation and purity assurance. Industry compliance standards
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On the factory floor, every batch of Ethyl Iodoacetate carries a set of expectations and a measure of pride. This compound stands out in our line of alkylating agents due to its unique carbon-iodine bond, which shapes how chemists and researchers use it across settings like pharmaceutical development and fine chemical synthesis. We have watched the demand for Ethyl Iodoacetate shift from being a niche reactant to a staple in many labs seeking precise chemical transformations.
Creating alkylating agents such as Ethyl Iodoacetate takes more than reading specs or sourcing raw materials. Production runs involve careful temperature control, strict moisture exclusion, and experienced hands to ensure everything reacts as intended. Standing in the reactor room, one sees why the purity of our Ethyl Iodoacetate matters: minute amounts of water or impurities can send yields tumbling and introduce byproducts that haunt downstream users.
We consistently produce Ethyl Iodoacetate in colorless to pale yellow liquid form, using reaction setups that handle iodine's sensitivity to light and moisture. The final product goes through multiple distillations and thorough quality checks. By the time the containers are sealed and sent to customers, every detail has been checked—starting from the assay, tested above 98% by standard methods, to guarantees around minimal residue and specific gravity. A manufacturer with years logged at the reactor knows where shortcuts lead. For Ethyl Iodoacetate, there’s just no substitute for vigilance from start to finish.
There’s a difference between listing specs and living with the consequences. In lab-scale reactions, chemists need to know about how quickly Ethyl Iodoacetate reacts with nucleophiles, which often comes down to the way it’s made and stored. From a supplier’s view, shelf life correlates with both moisture control in production and container sealing at the plant. For products headed into pharmaceutical syntheses or custom peptide work, any side impurities can complicate separations and degrade the quality of the end molecule.
Our regular lot analysis covers boiling point, refractive index, and acid-base titration to confirm ester content, but experience fills in where numbers alone can’t. For instance, repeated feedback from process chemists taught us that batch-to-batch consistency matters more than squeezing another 0.5% purity rating. Users blend our Ethyl Iodoacetate into reactions banking on that reliability; no one enjoys halting scale-up efforts because one drum doesn’t match the last.
Ethyl Iodoacetate finds its way into a surprising range of applications. We’ve talked with researchers using it to introduce an iodoacetate moiety onto amino acids, generating intermediates for pharmaceuticals and custom small molecules. In protein chemistry labs, it helps in modifying cysteine residues for site-selective labeling, exploits made possible by its clean, predictable alkylation ability. We see orders trending upward from companies involved in the next wave of drug targets, where robust building blocks matter in the rush to bring new therapies forward.
Some industrial partners turn to Ethyl Iodoacetate for its role in synthesizing herbicides or insecticides, leveraging the iodo group for subsequent transformations. Its effectiveness in these routes depends on how reliably it delivers: off-target reactivity or contaminants can throw entire campaigns off track. Our own process improvements—moving toward greener reaction solvents and improving waste minimization—come from these real-world demands.
The world of alkyl halides comes packed with options. Ethyl BroMoacetate, Ethyl Chloroacetate, and the methyl analogues all offer different reactivity and safety profiles. Iodoacetate esters like ours react fastest, which is critical for time-sensitive work but demands careful storage to keep degradation at bay. Longer experience has shown that while bromide or chloride versions can sometimes replace the iodide, they rarely match the clean snappiness shaped by iodine’s lower bond strength.
As a bulk producer, we see the full circle—from orders requiring small, research-sized bottles to custom drums filling entire palettes for kilo-scale syntheses. Many partner labs request our Ethyl Iodoacetate over its bromo and chloro cousins for one reason: the rate and selectivity of the reactions support smoother downstream processing. It’s about reducing the cost of corrections and boosting the chances that a process, whether for a drug intermediate or a specialty material, works as intended from the start.
Comparing across options, Ethyl Iodoacetate also introduces less corrosivity against certain reactor linings than the brominated version. Over the years, we’ve worked with maintenance engineers who appreciate that distinction—saving them time and repair costs, especially when running repeated cycles or working at elevated temperatures.
After years of fine-tuning, our Ethyl Iodoacetate comes backed by process controls that matter to chemists who stake their results on specifying even small variables. We analyze every batch for critical parameters, not because a manual demands it, but because repeat production has shown that slight differences upset whole workflows. End users rely on us not just for labeled content, but for the judgment—we know what side products might lurk, and we test for them.
Our facility’s approach rests on a foundation built on regular maintenance, solvent recycling, and operator training. Those sweating in the production area work with Piperidine and Glycol reactants at temperature gradients that make small talk impossible. Here it’s common knowledge that subtle shifts, like the timing of reagent addition or a five-degree deviation on a heating mantle, can alter not only yield but also the stability of the finished compound. Such operational experience informs every specification behind the Ethyl Iodoacetate we send out.
Not every customer works at the same stage of discovery. In academic settings, we receive reports of Ethyl Iodoacetate turning up in mechanistic studies and in enzyme inactivation research. Sometimes, students and junior postdocs call for insight about handling and storage. Based on decades’ practice, we emphasize storing this compound in amber glass, desiccated, in cool rooms, and keeping it away from base vapors—environments that might foster decomposition.
On the scale-up side, pilot plants run test batches, observing how the reagent fares under varying solvent conditions or under continuous flow. We collect feedback on reaction conversions, chromatic purity, and isolated yield. Often, tweaks to our drying step or even a one-hour adjustment to the reaction hold can improve these outcomes. So, while our baseline product meets high standards, we learn every year how to adapt, because R&D chemists need answers in real time, not just product releases and data sheets.
Manufacturing specialists routinely ask about the environmental effects—what happens to Ethyl Iodoacetate as waste or after use. We acknowledge that as an alkylating agent, it poses both safety and environmental concerns, especially if handled improperly. Production staff train rigorously for spill control and accident prevention, limiting vapors and using containment systems to keep any releases within the plant boundaries.
Over the years, we have replaced more hazardous methods with contained systems and introduced safer loading areas. Spent Ethyl Iodoacetate and wash residues go for incineration under controlled conditions, guided by legislation and practical experience with halogenated esters. While regulations continuously shift, our practices get shaped by hands-on lessons from previous generations of chemists and plant operators: job safety doesn’t just mean gloves and goggles, but understanding fumes, storage compatibility, and the limits of common neutralization methods.
Across borders, regulatory authorities push for tighter control and more transparent supply chains. Our Ethyl Iodoacetate runs through compliance screens—from hazardous shipment labelling to certifications for product quality and batch traceability. Handling export shipments and customs documentation brings new challenges. Sometimes, a three-page document review finds a gap that would delay an order for weeks. We keep product and process documentation clear, so investigators at customs or regulatory audits can track each drum back to its earliest production record.
International partners regularly request documentation around production conditions and storage details. Having switched from handwritten batch logs to electronic tracking, we can quickly produce proof of testing and source provenance. Trust with long-term buyers grows from such transparency, and it takes constant attention to maintain.
We understand Ethyl Iodoacetate beyond just putting bottles on shelves. Our team does more than list products in a catalog—chemists step in to field questions about solvent selection, possible degradation routes, and work-up advice. Years spent troubleshooting reactions taught us that an experienced voice can sometimes solve problems faster than trial and error.
Support often involves discussing alternatives—for instance, examining if a user really needs the cleaning power of a high-grade Ethyl Iodoacetate or if a less-reactive ester fits a more routine task. By understanding reaction tolerances and endpoint requirements, we help minimize waste and avoid unnecessary costs. This kind of collaboration grows out of long relationships, where reliability carries more weight than price.
Manufacturing never stands still. We keep improving Ethyl Iodoacetate production through newer reactor designs, automated metering, and in-line analytical controls. The shift toward continuous processing helps us cut waste and offer more options for custom batch sizes. Plant engineers introduce steps that increase reaction safety, such as nitrogen blanketing and real-time vapor monitoring, to head off incidents before they start.
Upgrades come with challenges; sometimes, a process change aimed at improving throughput means revalidating purity levels or finding better materials for storage drums. We invest in these upgrades not because a brochure demands it, but because the long run supports both business and responsibility. Plant workers, technical staff, and quality controllers meet routinely to review outcomes and share points for improvement. Some changes stem from customer input, others from our own drive to make things safer and more efficient.
Users benefit from understanding what sets high-quality Ethyl Iodoacetate apart. Clear, stable product lets you skip unnecessary re-purification steps, and confirmed batch consistency shaves off delays in synthesis. We stress the value of asking for recent batch data—real manufacturers don’t hesitate to share results because they know the value of every test.
For those new to working with halogenated esters, handling guidance matters. We advise storing containers in tightly closed bottles, using inert gas overlays if long-term storage is needed. Keeping chemicals in cool, dry spaces minimizes the breakdown that leads to acid formation and yellowing. In production, plant teams rotate inventory so nothing sits beyond its optimal shelf life.
Years of steady demand have confirmed Ethyl Iodoacetate’s value—not just for its role as an alkylating agent, but for the reliability it brings into process development. Its application base keeps broadening; research fields that once relied on other acetates start seeking out the faster, more predictable reactions possible with the iodo version.
Partner labs and scale-up groups come back for the same reason: clean chemistry makes for easier separations, fewer failures, and better overall throughput. From the first blend in our mixing tanks to the care spent filling each container, every batch represents accumulated lessons. We believe that a manufacturer’s value shows in the results chemists achieve—not just in what our labels say, but in the real differences seen at the bench, in the pilot plant, and on production lines around the world.