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HS Code |
578301 |
| Chemicalname | Acetyl Iodide |
| Iupacname | Ethanoyl iodide |
| Chemicalformula | C2H3IO |
| Molarmass | 170.95 g/mol |
| Casnumber | 507-02-8 |
| Appearance | Colorless to pale yellow liquid |
| Boilingpoint | 105 °C |
| Meltingpoint | -50 °C |
| Density | 2.29 g/cm³ |
| Refractiveindex | 1.607 |
| Solubilityinwater | Reacts with water |
| Vaporpressure | 30 mmHg (25 °C) |
| Flashpoint | 27 °C |
| Odor | Pungent |
| Stability | Unstable in presence of moisture |
As an accredited Acetyl Iodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of Acetyl Iodide, tightly sealed, labeled with hazard symbols, chemical name, and handling instructions. |
| Shipping | Acetyl Iodide should be shipped in tightly sealed, corrosion-resistant containers under nitrogen or an inert atmosphere. It must be protected from moisture and heat, and transported as a hazardous material according to international regulations (UN1714). Appropriate hazard labels, documentation, and emergency procedures must accompany the shipment to ensure safe handling during transit. |
| Storage | Acetyl iodide should be stored in a tightly sealed, amber glass container under an inert atmosphere, such as nitrogen or argon, to prevent decomposition. Keep it in a cool, dry, and well-ventilated area, away from heat, moisture, light, acids, and bases. Store separately from oxidizing agents and water, as it reacts violently with water, producing toxic and corrosive byproducts. |
Applications of Acetyl Iodide in Industrial ManufacturingAcetyl iodide serves as a specialty raw material in several targeted industrial sectors, with each application requiring strict process management and controlled conditions. As a direct manufacturer, we supply this reagent for processes where precision, purity, and compliance with regulatory standards are critical to final product quality. 1. Active Pharmaceutical Ingredient (API) SynthesisManufacturers use acetyl iodide in iodination and acetylation reactions during multi-step API synthesis, particularly for small molecules containing iodoacetyl functionalities. The reagent functions as a key acetylating and iodinating agent at defined process steps, enabling precise substitution to form molecular scaffolds required for antiviral, antifungal, or anticancer drug intermediates. Consistent quality and accurate delivery rates are essential to minimize byproduct formation and ensure API purity per regulatory standards. Industry compliance standards
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2. Agrochemical Intermediate ManufacturingAcetyl iodide enters the synthesis of iodinated intermediates used in the formulation of selective herbicides and insecticides. Chemical processing requires exact reagent flow control, since over-iodination impacts product selectivity and environmental compatibility. Safe handling and containment procedures ensure the final intermediates are fit for further conversion to registered agrochemical actives. Industry compliance standards
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3. Specialty Aromatic Ester ProductionChemical plants use acetyl iodide for esterification of aromatic hydroxyl compounds, especially when milder acylation reagents fail to achieve full conversion due to substrate specificity. Its unique reactivity profile supports the synthesis of high-purity esters needed in fine fragrance and specialty chemical applications. Stringent emissions control and product isolation practices apply in this segment due to potential iodine volatilization and odor impact. Industry compliance standards
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4. Laboratory-Scale Fine Chemical SynthesisAcetyl iodide supplies academic and research-scale development work, especially for preparing reference standards, introducing iodoacetyl groups, and assessing new synthetic methodologies. Small-lot production often serves R&D projects requiring rapid turnaround and high material purity, supporting robust analytical and analytical method validation protocols. Industry compliance standards
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Acetyl iodide has earned a reputation as a reagent that brings clarity to specific synthetic steps in organic chemistry. In the production halls and laboratories where we prepare this clear, colorless-to-pale-yellow liquid, experience reminds us that seemingly small decisions—choice of solvent, temperature, order of operations—produce a large impact on outcome. Over the decades, we have witnessed acetyl iodide moving from the status of an academic curiosity to a trusted tool for methylation, iodination, and acylation steps in commercial-scale synthesis.
The characteristic sharp, pungent odor of acetyl iodide tells the story of a molecule ready to react. In our facilities, we craft it through direct halogenation of acetic anhydride with iodine, ensuring purity that matches the most demanding research and manufacturing workflows. Each batch faces rigorous impurity and moisture testing. Stability always rides on strict moisture control: any contact with water leads to rapid hydrolysis, so transport and storage systems remain rigorously dry and airtight—no compromise.
Every specification we list has a story. Through experience, 97–99% purity is the minimum required to guarantee reactivity and yield. Acetyl iodide’s boiling point sits at roughly 100–102°C; because of this, standard laboratories require careful containment and deliberate atmospheric controls. Density, around 2.28 g/cm³, doesn’t just fill a line on a datasheet—it dictates how we design pumping, metering, and filling systems, especially for kilo-scale batches.
We never treat shelf-life as a marketing statistic. Acetyl iodide starts to decompose if left open to air, evolving acetic acid and free iodine. Over time, the subtle vapor pressure increase inside a sealed bottle signals unseen reactions if moisture ever sneaks in. Our product leaves our doors in dark amber glass containers, tightly sealed and purged with an inert gas, because years of shipping and handling mishaps taught us that even small details catch up in the end.
Chemists who know acetyl iodide recognize it as an acylating and iodinating agent with deliberate roles in organic synthesis. From benchtop flask to pilot plant, it’s often introduced to transform alcohols to alkyl iodides through the so-called Appel-type reactions. The in-situ formation of alkyl iodide eliminates the isolation of unstable intermediates, streamlining flows for manufacturers scaling up from grams to tons. Pharmaceutical synthesis, especially for specialty active ingredients with iodinated substructures, benefits from the directness and speed that acetyl iodide brings to the table.
Experience with other reagents—acetic anhydride, acetyl chloride, and phosphorus triiodide—offers useful comparison. Acetyl iodide stands apart for those who require an efficient acyl source that doesn’t flood the system with unwanted side products or excessive acidity. It works cleaner in environments where sensitive functional groups dictate the choice of acylation reagent. In peptide modification and certain aromatics functionalizations, the exact reactivity window of acetyl iodide means fewer protection/deprotection cycles, less purification, and more predictable yields. Real-world chemists rarely appreciate expensive surprises in late-stage synthesis, so superior selectivity counts.
For decades, the main alternatives to acetyl iodide have been acetyl chloride and acetic anhydride. Both play roles in acyl transfer, yet the differences come out in yields, by-product profile, and downstream process difficulty. Acetyl chloride often gives off hydrochloric acid, causing corrosion and requiring extra neutralization and ventilation. Acetic anhydride can be less reactive in some contexts, leading to unreacted starting material—or requiring prolonged heating, risking product degradation. Acetyl iodide, with its more controlled release of iodide and acetyl, often provides a middle path. We’ve found that the material’s reactivity at room temperature can save energy and reduce safety risk compared to harsher chlorination or anhydride chemistry.
Phosphorus triiodide’s reputation in iodination chemistry is well-established, but the handling difficulties—pyrophoricity, highly exothermic reactions—make it unpopular in scale-up except for specialized plant environments. Acetyl iodide provides similar transformations without the strong reducing environment or phosphorus waste stream. No chemist wants to open process vessels and see red phosphorus gums or run into hard-to-dispose halide waste. Where iodine exchange reactions matter, acetyl iodide keeps the process simple.
Safety does not live in back-page footnotes. Any user working with acetyl iodide experiences vapors that can cause serious irritation to skin, eyes, and respiratory system. In our manufacturing rooms, even tiny spills or accidental exposure lead to rapid clean-up and containment under chemical hoods. Time in full PPE and with constant monitoring isn’t only for regulatory compliance—it is the lived reality of chemists who learned that underestimating fume toxicity invites real risk. Technicians and researchers in our plant go through yearly refreshers focused specifically on halide acyl reagents. Our accident records show significant reductions since we adopted double-seal transfer vessels and real-time vapor concentration sensors. Teams know the rules not just because of policy, but because old habits die hard and the consequences for getting complacent have always been steep.
Material compatibility plays an unsung but crucial role in both large and small operations. Acetyl iodide reacts readily with most metals besides glass, Teflon, or coatings designed to resist aggressive halogens. Over time, we retrofitted our plant glassware system with ground glass joints and PTFE gaskets simply because earlier screw-top systems corroded too quickly, releasing iodine vapor and shortening equipment life. Customers in pilot plants who once thought “good enough” materials would last learned firsthand about gasket swelling, sticky residue, and valve failures. Detailed knowledge of compatible materials is an earned edge.
From gram-scale research to multi-ton reactors, the journey with acetyl iodide relies on process consistency. In early years of scale-up, variations in reaction temperature and small trace impurities led to batch failures. Monitoring incoming feedstock and developing our in-house purification improved both reliability and customer trust. Today’s batches undergo in-line NMR and Karl Fischer titrations for water content, all corrected in real time before bottling. It’s not just boxes checked for quality assurance; we remember failed campaigns, reprocessing costs, and lost weekends that propelled us to invest in that technology.
Reactors and transfer lines in our plant feature continuous monitoring for both pressure and vapor composition, because exothermic hydrolysis remains the top uncontrolled hazard. Sticking to process recipes doesn’t guarantee safety if monitoring lags. Each new customer who approaches increased scale receives guidance based on lessons: gradual addition, staged venting, and plenty of inert blanket, all drawn from genuine learnings rather than wishful theory. Trust only flourishes between chemist and supplier when both sides openly exchange process pitfalls.
Manufacturers and researchers want more than raw materials; they need reliability and performance. Time and again, customers push back against poor lot-to-lot consistency or mysterious contamination. Too many promising syntheses falter due to a bad batch, especially near deadlines. Our plant adopted batch traceability and cross-lot analytics to catch drifts before customers ever notice them. If technical staff see a trend toward lower reactivity or color shift, it prompts immediate root cause investigation instead of waiting for end-use complaints.
In a world where supply chain shocks delay or reshape research, keeping acetyl iodide available depends on real, hard-earned fundamentals: always keep raw iodine in stock, stay ahead of solvent shortages, and train workers who know every nuance of filling and sealing. Reactivity does not forgive shortcuts. Chemists using our acetyl iodide deserve lots that match the last, that pour cleanly, react predictably, and arrive packaged with real-world handling in mind.
Global scrutiny of halogenated reagents and their by-products calls for responsible manufacturing. For acetyl iodide, efficient use of raw iodine, minimized fugitive emissions, and careful waste stream control guide how we run our plant. Our operations focus on maximizing batch atom economy. We recycle spent iodine, recover acetic acid, and scrub vent lines. Not every process provides straightforward waste solutions, but we have found that adopting green chemistry principles at the outset opens new markets while avoiding the headaches of regulatory catch-up. For pharmaceutical partners seeking to keep iodinated impurities and halide levels within specification, working with an upstream supplier who shares these values means fewer surprises and easier regulatory filing.
Regulators continue to tighten discharge limits on iodinated organics, so every batch run involves steps to neutralize and recover excess iodine in a tightly managed water stream. Investing in closed-loop waste management addresses both compliance and operational cost. Years of experience have shown that skimping on recovery comes back as an expensive mistake—it should never be treated as an afterthought to meet minimum codes. Our teams track and optimize every step, reducing batch losses and environmental impact while extracting more value from feedstocks previously written off as waste.
The demand for fluorinated and iodinated building blocks follows a steady rise, driven by specialty pharmaceuticals and agrochemicals. As the world moves toward more targeted therapies and advanced materials, the fine-tuning possible with agents like acetyl iodide cannot be underestimated. Acylation chemistry remains foundational, especially with persistent need for selective, mild conditions. By mastering its quirks and optimizing every handling step, we secure our place as a reliable supplier to scientists on the frontier of industrial, academic, and commercial chemistry.
Many products come and go through trends, but acetyl iodide maintains relevance by offering a balance between reactivity, selectivity, and manageable hazard profile. It complements new techniques including flow chemistry, where predictable response to mixing rates, temperature jumps, and quick quenching are essential. Our own innovation pipeline has seen growing application for this reagent in continuous processing setups, where traditional batch risks—from vapor accumulation to side reactions—are inherently reduced.
Over time, our technical support teams have collected case studies from clients across pharmaceuticals, specialty fine chemicals, and research institutions. Some projects succeed on the first run; most improve through matchmaking between product properties and real process needs. Users report that acetyl iodide’s sharper reactivity profile means shorter reaction times, less heating, and easier work-up of products in otherwise stubborn conversions. The price for skipping controlled addition or failing to keep a moisture barrier, though, reveals itself in lower yield and tough-to-purify batches. Our documentation and advisory support draw from both textbook knowledge and the hands-on lessons our operators learned through error and revision.
Logistics remain just as critical as chemical compatibility. We pack and ship only with specialty-certified carriers trained for hazardous organics, reinforced by our own audits and periodic surprise inspections. Experience taught us that relying too heavily on generic transit partners leads to heartbreak—broken packaging, unexpected delays, and regulatory headaches slow down research and production. Even small investments in better packaging, tamper-evident closures, and tracked shipments pay dividends to customers chasing critical timelines.
Competitors can offer “similar” acyl halides or even generic acetyl iodide made through unchecked routes, but the lived difference comes down to know-how earned through repetition, error, and refinement. Through years where new process hazards, raw material volatility, and shifting customer expectations challenged our status, we doubled down on transparency. Customers expect stability, actionable documentation, and the ability to reach knowledgeable chemists—not boilerplate or fine print.
Acetyl iodide bridges the gap between older, less precise halogenating reagents and new, more sensitive synthetic strategies. Its special balance of speed, selectivity, and controllable hazards makes it dependable for challenging synthetic transformations, whether in industrial or high-end research settings. Those who work with it daily—operators, support staff, customers—know the difference: fewer batch failures, less downtime, and smoother, cleaner processes.
Our efforts follow a simple truth: details matter, and long-term users remember who delivers product matched to real-world, daily needs. Every batch of acetyl iodide reflects lives invested in chemical handling, safe process engineering, and robust operational protocols. We continually upgrade our plant processes and invest in people who understand not just what the product does, but how it fits in the intricate web of modern synthesis.
Feedback from researchers and process engineers—good and bad—shapes our next steps. Whether your need centers on gram-scale experiments or reliable tonnage for manufacturing, our team stands ready to share practical lessons and build success on the back of honest experience.