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HS Code |
386501 |
| Chemical Name | Acetyl Iodide |
| Iupac Name | Iodoethanone |
| Molecular Formula | C2H3IO |
| Molar Mass | 169.95 g/mol |
| Cas Number | 507-02-8 |
| Appearance | Colorless to pale yellow liquid |
| Density | 2.129 g/cm³ |
| Boiling Point | 97-99 °C |
| Melting Point | -84 °C |
| Solubility In Water | Decomposes |
| Refractive Index | 1.610 (20 °C) |
| Vapor Pressure | 55 mmHg (25 °C) |
As an accredited Acetyl Iodide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Acetyl Iodide is packaged in amber glass bottles, 100 mL size, with tamper-evident caps and clear hazard labeling. |
| Shipping | Acetyl iodide should be shipped in tightly sealed, corrosion-resistant containers, protected from moisture and light. It must be clearly labeled, handled as a toxic and corrosive substance, and transported according to regulations for hazardous chemicals. Ensure the package is upright, with proper ventilation, and separated from incompatible materials like oxidizers and bases. |
| Storage | Acetyl iodide should be stored in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. Keep it in tightly sealed glass containers, protected from moisture and incompatible substances such as water, alcohols, and strong bases. Proper chemical storage cabinets, preferably for corrosive or reactive chemicals, are recommended. Clearly label containers and prevent exposure to air. |
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Purity 98%: Acetyl Iodide with purity 98% is used in organic synthesis laboratories, where it ensures high-yield acetylation of alcohols and amines. Boiling Point 105°C: Acetyl Iodide with a boiling point of 105°C is used in acylation reactions, where it allows controlled and efficient reaction conditions. Reagent Grade: Acetyl Iodide of reagent grade is used in pharmaceutical intermediate production, where it facilitates reliable formation of acetylated precursors. Moisture Content <0.2%: Acetyl Iodide with moisture content less than 0.2% is used in moisture-sensitive chemical synthesis, where it prevents undesirable hydrolysis and maintains product integrity. Stability Temperature 0–4°C: Acetyl Iodide stored at a stability temperature of 0–4°C is used in research laboratories, where it offers prolonged shelf life and consistent reactivity. Density 2.1 g/cm³: Acetyl Iodide with density 2.1 g/cm³ is used in analytical chemistry protocols, where it provides precise volumetric measurements for reagent formulation. |
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Acetyl iodide, chemical formula CH3COI, stands out among organoiodides for its strong reactivity and niche usage in organic synthesis. From the manufacturing floor, we recognize that customers from research to scale-up settings depend on this highly sensitive compound for reactions that require a precise introduction of acetyl groups where milder agents cannot deliver the same results. Working with acetyl iodide—often referred to simply as "acetylating agent" in our labs—means keeping careful watch on every batch and molecule, since both its benefits and challenges set it apart from acetic anhydride, acetyl chloride, and other acetyl donors.
The physical properties of acetyl iodide demand respect from all who handle it. Since its boiling point sits comfortably below 115°C and it decomposes in the presence of air or water, the product leaves our facility packed under inert gas in chemically resistant glass. Purity is a central point—where even a touch of hydrolysis can introduce free iodine and acetic acid, pulling the reactivity away from intended synthetic targets. We regularly achieve and monitor purity levels above 98%, using rigorous in-house gas chromatography and titration checks. Laboratory customers and industrial users alike come to us seeking this assurance; only consistent purity enables reproducible results and minimization of byproducts in syntheses.
Production scale differs from bench-top scale. Having supplied both kilo-labs and large-scale campaigns, we understand the need for reliable packaging—a single 50-gram amber glass bottle for research work, multi-liter lots for process chemists, and custom filling options for pilot projects. We adjust fill sizes prudently, avoiding oversized stock that could increase exposure and lead to product degradation (especially problematic with such a sensitive reagent). Our glass packaging always includes PTFE-lined stoppers, minimizing moisture ingress without introducing compatibility issues found with some plastics. For larger requirements, stainless steel and glass ampoules provide safe alternatives.
Our experience making and supplying acetyl iodide has shown that the route to a clean, high-yielding reaction depends on technique and knowledge just as much as the starting materials themselves. Because acetyl iodide reacts rapidly with water to form hydrogen iodide and acetic acid, every stage—from dispensing through reaction addition and workup—calls for a dry, inert atmosphere. In the hands of skilled chemists, the reagent forms esters and amides under milder conditions than acetic anhydride or acetyl chloride, with iodide acting as a superior leaving group. We have seen customers in the pharmaceutical field choose acetyl iodide for challenging acetylations of hindered alcohols or amines, often finding faster rates and higher purity compared to other reagents.
Our technical support team frequently answers questions about best practices for using acetyl iodide. We suggest minimizing headspace exposure, using dry solvents, and maintaining reaction temperatures below the decomposition threshold. We often caution against attempting direct addition to aqueous mixtures, since hydrolysis wastes reagent and can create overpressure in sealed systems from evolved gas or iodine vapor. In our own kitchens, so to speak, we practice what we preach: even small scale operations take care to purge reaction vessels with argon or nitrogen before, during, and after acetyl iodide addition.
For many years, our customers have asked bluntly why use acetyl iodide instead of classic acetyl chloride or acetic anhydride. The answer is simple if you have ever tried acetylating a stubborn phenol, carbohydrate, or secondary amine: iodide’s leaving group ability changes the landscape of the reaction. Acetyl iodide often gives higher conversion and cleaner product, particularly where steric hindrance blocks the approach of less reactive agents. On the flip side, acetyl iodide comes with a shorter shelf life, demands stricter storage, and brings a higher raw material cost due to use of elemental iodine.
In our own plant procedures, we keep the entire line for producing and handling acetyl iodide dry and oxygen free. Even a low-level leak can lead to rapid decomposition and loss of material. Comparing this to acetyl chloride reveals the core tradeoff: the chloride may last longer on the shelf and offer broader handling flexibility, but regiospecific reactions and challenging acetylation chemistry often call for the “overkill” power of the iodide reagent. For reactions that produce pharmaceutical intermediates or customized ester products in short timelines, the benefits in yield and purity often justify the extra handling steps. Success with acetyl iodide comes down to process discipline and an understanding of organohalide behaviors.
We have found most sales to academic laboratories, contract R&D outfits, and pharmaceutical manufacturers developing complex molecules. In recent years, the reagent has played a niche but crucial role in carbohydrate acetylation—the process of introducing protective acetyl groups to sugars, which would otherwise degrade under harsher conditions. The selectivity and speed of acetyl iodide can open up routes that fail with other agents; for example, protected glycosides and unusual amide linkages have been documented in published studies where only the iodide route produced clean enough yields for use as intermediates in multi-step synthesis.
On the industrial side, our own experience with process transfers has shown that acetyl iodide can improve throughput on specific campaigns, shaving time from post-reaction purification steps. This matters when producing clinical trial materials under time pressure—a difference of a single day may mean a lot to the end client. Because of the instability, we work closely with our partners for just-in-time delivery, ensuring the freshest possible reagent for their campaign, and thus minimizing the need to rework or discard precious intermediates due to over-aged stock.
It’s no secret that making acetyl iodide at scale poses significant challenges. We run dry-glass reactors under inert gas—no shortcuts or substitutes. Our plant draws upon rigorously tested iodine sources and acetic anhydride, using distillation and in-line gas scrubbers to contain corrosive off-gassing. Production shifts follow detailed inspection schedules. Over time, we learned that regular cleaning of transfer lines and venting systems cannot be overlooked. Each batch gets a full certificate of analysis, and we log every step taken during synthesis, allowing transparent traceability for regulated customers.
Waste handling deserves special mention. Iodine and its derivatives demand more than routine neutralization; capturing exhaust vapors and treating wash solutions properly helps avoid the environmental disasters of past decades. We work with certified disposal partners when discarding any iodide-bearing waste streams, sealing off possible exposure points for both the environment and the workforce. Year over year, we continue to invest in safer containment and transfer protocols. These choices reflect a greater responsibility than mere compliance—nobody wants a preventable incident or regulatory fine setting back hard-earned business or academic relationships.
We sometimes field questions about why buy this reagent instead of making it on-site. From our side, stability and analytical data form the backbone of our service. In a production environment, the risk of cross-contamination or residual byproducts from hastily prepared reagent runs high. Over the years, we've seen projects delayed by trace water contamination, sloppy distillation, or inadequate containment—troubles which commercial batches sidestep through purpose-built infrastructure and decades of experience.
We have worked closely with research groups moving from proof-of-concept to pilot scale and learned plainly: At small scale, home-cooked acetyl iodide serves for quick tests. Past that, batch-to-batch reproducibility, safety assurances, and supply security all benefit from dedicated manufacturing. Our customers value up-to-date certificates of analysis, tighter control of impurities, and responsive after-sales technical help. Scalability, ironically, often means handing the job back to specialists with both the right glass and a deeper understanding of iodine’s quirks.
Experience teaches that international shipments of acetyl iodide present their own hurdles. Many routes subject shipments to dual-use regulations, hazardous goods checks, and customs inspection. We've learned that an incomplete or inaccurate manifest creates customs delays and material loss. That's why we pack every export in UN-certified containers, clearly labeled, with full supporting documentation. We've shipped to every continent except Antarctica, but only after pre-clearance with customers to prevent regulatory surprises at borders.
More customers now explore acetyl iodide for specialized carbonylation chemistry and as a precursor for further iodo-organic transformations. In each case, rapid feedback from our technical support team helps shape next steps. Sometimes a new customer shows us a research article or patent, then asks, “Can it be done at our scale?” Our in-house chemists supply data on solubility, stability, and compatible reaction conditions. We've even tailored pack volumes to minimize excess waste for these pilot efforts. Our troubleshooting includes product lifespan in different temperatures, advice for cold-chain logistics, and tips for maximizing yield in microgram-quantity operations.
One lesson reinforced in our production lines is that strong adherence to safe handling protocols does not come from paperwork—it's habits and continual training. Each operator on the acetyl iodide line receives specific instruction in the reactivity and risks of iodinated reagents. We supply them with the best PPE, monitor air quality in use zones, and regularly review emergency procedures for spills and pressure surges. Yearly audits review protocols for possible gaps, with direct input from workforce and local safety authorities. Recent upgrades include double-seal transfer lines and enhanced ventilation, based on employee feedback after minor vapor leaks. The safer the working environment, the more reliable the product and the smoother the logistics for the end user.
Even with top-tier manufacturing, shelf life remains a key concern. We label every bottle with a clear fill date and recommend storage under dry nitrogen between 2°C and 8°C. Based on our stability studies, unopened containers retain full utility for up to three months, while partial bottles show clear signs of decomposition after just a week of frequent ambient access. Picture a high-volume lab using a liter per week—they keep cold-storage cabinets near their workstations, and feed lines connect directly to glass reactors, limiting time spent open to air. Through collaboration with such customers, we've refined our packaging and shipping processes to align product turnover with best-practice handling, minimizing risk of over-aged stock and waste.
The legacy of organoiodides includes tales of mishandled waste and chronic exposure. We operate in a new era, where environmental regulators expect more, and customers share that outlook. Our plant’s emission controls have earned positive marks during routine local environmental audits. We ensure every drum of waste enters a closed-loop handling system. We educate downstream users on proper quenching, neutralization, and collection of iodide-bearing residues—because our interest extends beyond sale to final use and disposal. Customers doing scale-up work receive current documentation on waste mitigation, spill response, and compatible neutralizing agents, shaped by both local and international guidelines.
We have seen unique projects flourish thanks to the selectivity and raw power of acetyl iodide—new catalysts, protected building blocks, short-lived intermediates that would never survive harsher chemistry. Research clients have shared their results with us, and we take pride in playing a small role in pushing the limits of known synthesis. Whether we support an academic breakthrough or a new generative process in a big manufacturing campaign, our team brings respect for both the tradition and the future of chemical production. Feedback from our partners influences our continuous push for process refinement and new application notes, so every batch benefits from a living knowledge base within our company.
We believe manufacturing acetyl iodide is never just about filling a bottle and putting it on the truck. It is about supporting the ambitions of chemists who need a sharper tool, ensuring supply lines stay up even through regulatory or logistical interruptions, and keeping both human and environmental safety at the center of every operation. Our investment in both process and people makes us a partner in innovation. We see acetyl iodide not as a commodity, but as a crafted reagent whose true utility emerges from reliable, responsive manufacturing and a willingness to solve problems large and small. Each shipment is a reflection of our commitment to the craftspeople and visionaries transforming raw molecules into tomorrow’s breakthroughs.