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Acetyl Chloride

    • Product Name Acetyl Chloride
    • Alias Ethanoyl chloride
    • Einecs 201-851-8
    • 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
    Specifications

    HS Code

    626207

    Chemicalname Acetyl Chloride
    Iupacname Ethanoyl chloride
    Chemicalformula C2H3ClO
    Molarmass 78.50 g/mol
    Appearance Colorless to pale yellow liquid
    Odor Strong, pungent, irritating
    Meltingpoint -112 °C
    Boilingpoint 51 °C
    Density 1.104 g/cm³ at 20 °C
    Solubilityinwater Reacts violently
    Vaporpressure 224 mmHg at 20 °C
    Casnumber 75-36-5
    Flashpoint -20 °C (closed cup)
    Refractiveindex 1.389 at 20 °C
    Hazardclass Corrosive

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

    Packing & Storage
    Packing Acetyl Chloride is packaged in a 500 mL amber glass bottle with a tightly sealed cap, labeled with hazard warnings.
    Shipping Acetyl chloride must be shipped as a hazardous material in tightly sealed, corrosion-resistant containers under cool, dry conditions. It should be isolated from water, alcohols, and other incompatible substances. Proper UN labeling (UN 1717), documentation, and compliance with all local, national, and international transport regulations are required.
    Storage Acetyl chloride should be stored in a cool, dry, and well-ventilated area, away from moisture, heat, and direct sunlight. It must be kept in tightly sealed glass containers with non-metallic screw caps, as it reacts violently with water and moisture, releasing corrosive hydrochloric acid fumes. Store separately from bases, acids, oxidizing agents, and alcohols to prevent dangerous reactions.
    Application of Acetyl Chloride

    Purity 99%: Acetyl Chloride with a purity of 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and purity of active compounds.

    Low Moisture Content: Acetyl Chloride with low moisture content is used in acetylation reactions in agrochemical manufacturing, where it minimizes side reactions and improves reaction efficiency.

    Density 1.104 g/cm³: Acetyl Chloride with a density of 1.104 g/cm³ is used in laboratory-scale acetylation processes, where it enables precise volume-based dosing for reproducible results.

    High Reactivity: Acetyl Chloride exhibiting high reactivity is used in polymer modification applications, where it facilitates rapid introduction of acetyl groups for targeted property enhancement.

    Stability Temperature 5–25°C: Acetyl Chloride maintained at a stability temperature of 5–25°C is used in API (active pharmaceutical ingredient) production, where it prevents decomposition and maintains product integrity.

    Volatility: Acetyl Chloride with high volatility is used in organic synthesis for acylation, where it allows efficient removal by evaporation and reduces process residue.

    Colorless Appearance: Acetyl Chloride with a colorless appearance is used in fine chemical manufacture, where it eliminates risk of color contamination in finished products.

    Molecular Weight 78.5 g/mol: Acetyl Chloride with a molecular weight of 78.5 g/mol is used in flavor and fragrance synthesis, where it ensures predictable reactivity and product consistency.

    Corrosivity: Acetyl Chloride with notable corrosivity is used in catalyst preparation, where controlled reactivity assists in activating catalytic sites on carrier materials.

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    Certification & Compliance
    More Introduction

    Acetyl Chloride: Driving Change in Chemical Processes

    Why Acetyl Chloride Matters in Everyday Chemistry

    Acetyl chloride pops up more often in industry conversations than many people assume. This isn't just another chemical moving quietly through laboratory shelves; its sharp, pungent odor and high reactivity with water make it a staple reagent for chemists working with organic compounds. People sometimes overlook this molecule because they confuse it with more benign acetates. But acetyl chloride plays an entirely different game. Its chemical structure, CH3COCl, creates a versatile platform for introducing acetyl groups into bigger molecules—something pharmaceutical and agrochemical manufacturing rely on.

    Having worked with students trying to grasp organic synthesis, I've noticed how quickly their respect grows for this compound after the first run-in with its aggressive nature. Pouring acetyl chloride into a beaker of water doesn’t lead to gentle fizzing; it reacts instantly, releasing hydrochloric acid fumes that sting the nose and the eyes. While this sounds dangerous, this reactivity forms the backbone for so many important chemical reactions. The lab’s need for responsible handling shouldn’t overshadow the value acetyl chloride adds—it can turn a mediocre synthesis route into something efficient, streamlining processes that used to be drawn out and expensive.

    Putting Acetyl Chloride to Work

    Small-scale users in university labs and massive chemical plants both turn to acetyl chloride for one straightforward reason: it’s remarkably effective at making other chemicals. It shines in acetylation reactions, especially transforming alcohols and amines into acetates and amides. This leads directly to molecules central to everything from painkillers to herbicides. In the pharmaceutical world, acetyl chloride opens doors to more stable and bioactive molecules. For instance, turning a common pain reliever’s raw material into its finished form often uses acetyl chloride in the final acetylation step, ensuring purity and yield.

    Agricultural chemists also lean on this chemical. They need acetyl chloride to help create the active ingredients within crop protection agents. Its speed and selectivity make it hard to replace. In the dye and textile industry, using this compound ensures certain color-fast shades by acetylating dyes so they stick to fabric better.

    Consumer products benefit from its work, though few people outside the industry realize the connections. Think about everyday plastics, fragrances, or flavorings—many owe their properties to intermediates made using acetyl chloride. The supply chain quietly depends on it, which means ensuring a steady, reliable product becomes more urgent as technology pushes for purer, more efficient supply chains.

    Model and Specifications: The Practical Details That Matter

    Among various manufacturers, acetyl chloride tends to arrive at a guaranteed laboratory grade, often listing purity upwards of 99%, and with strict maximum limits on free acids or chlorine. This purity isn’t window dressing. Chemists talk about “spec’d reagents” because only the cleanest form allows for reliable, repeatable reactions. A batch with significant contaminants spells trouble—with unwanted byproducts undermining years of process development work.

    Packaging can be just as important as purity. Smaller glass bottles with tight seals end up in research settings where precision counts, while large-scale operations might receive drums lined with polymer coatings to keep the acid vapor from eating through storage material. This isn’t about marketing flash. Iron, plastic, and even some types of glass fall apart under the persistent attack of acetyl chloride fumes. A stable package preserves product quality and lowers the odds of a costly leak during storage or transit.

    How Acetyl Chloride Compares to Other Acylating Agents

    A graduate student once asked me why anyone would pick acetyl chloride over acetic anhydride or other acyl halides. The answer rarely comes down to just price. Acetyl chloride stands out for a few reasons. It reacts more aggressively with nucleophiles, often driving reactions to completion faster than acetic anhydride, especially in stubborn cases where moisture sneaks into the workspace.

    Its lower boiling point—about 51°C—means it can be driven off easily during purifications or in distillation steps, leaving the desired product behind. On the flip side, this volatility can cause problems for handling and storage, especially in humid areas. Acetic anhydride, with a higher boiling point and less vapor production, seems gentler but sometimes disappoints during tough acetylations. Anyone who’s spent long hours in the lab knows this difference makes or breaks a schedule, especially near deadlines.

    Comparing acetyl chloride and thionyl chloride (SOCl2), for example, highlights a difference in byproducts. Thionyl chloride leaves behind sulfur dioxide and hydrogen chloride, gases that need to be scrubbed or vented safely. Acetyl chloride only generates hydrochloric acid and acetic acid, so the exhaust purification step might be easier to manage. Sometimes, the decision boils down to local regulations about emissions, or simply what a facility’s infrastructure can handle.

    Safety, Experience, and Industry Responsibility

    No commentary about acetyl chloride would be complete without reference to safety and responsible use. The chemical’s pungency alerts anyone in its presence about its power—there’s no silent risk here. Accidents involving acetyl chloride usually come from inattention or improvisation. As someone who’s watched more than one fume hood fog up during a rookie mistake, I can say with certainty: this is not the place for shortcuts.

    Proper training saves both careers and cash in this field. Roll out an acetyl chloride process without the right fume extraction, and corrosion sets in quickly—eat-throughs in lab benches, pitting in steel casework, or ruined ductwork result. At scale, careful design and routine equipment checks anchor a safe, productive facility. Modern chemical plants invest in remote sensors and acid-resistant gaskets to keep a tight lid on leaks, aiming to protect both workers and the surrounding community.

    Waste treatment isn’t a side note, either. Hydrochloric acid released from acetyl chloride reactions can cause serious environmental damage in large amounts. Industry leaders have moved away from old-school dumping or dilution, pushing for neutralization systems that recover valuable byproducts. Some sites recycle the acetic acid produced, closing a loop that makes the whole operation more sustainable.

    Innovation and Access: Looking Beyond Traditional Boundaries

    Chemicals like acetyl chloride don’t just stay in the hands of giant manufacturers. Smaller specialty chemical firms use it to develop custom molecules for medical research, electronic materials, or specialty coatings. The rise of on-demand sourcing and just-in-time inventory turns acetyl chloride into part of a flexible manufacturing ecosystem, matching global demand with new levels of efficiency.

    Researchers have started to reimagine how acetyl chloride can be made and handled. In some chemical engineering circles, continuous flow reactors are replacing big-batch syntheses. These systems cut down on waste and expose workers to smaller inventories at once, reducing overall risk.

    Efforts to replace or bypass acetyl chloride haven’t caught on in most applications simply because of the efficiency and selectivity it offers. Still, awareness of its hazards spurs ongoing work around personal protective equipment, storage solutions, and smart sensors—industry adaptation at its most practical.

    Regulation, Supply Chain, and Global Considerations

    Any company that handles acetyl chloride faces a raft of regulatory files. Governments recognize its risks. The European Union places it under REACH registration, while the United States closely tracks its shipping and usage for both industrial safety and anti-diversion reasons. These controls shape who gets to use acetyl chloride and under what circumstances.

    Right now, supply chain headaches create more worry than regulation. A hiccup in raw materials or shipping schedules sends ripples through pharmaceuticals and agriculture alike. Keeping a steady supply of acetyl chloride isn’t just about buying enough in advance. It means planning for single-source disruptions, finding backup options, and keeping an eye on global events—from port slowdowns to new trade rules.

    Some facilities have invested in on-site production of acetyl chloride to skirt shipping challenges. This shift lowers logistical headaches but raises new questions about local safety and waste handling. Others sign contracts with regional suppliers rather than international giants, aiming for shorter shipping routes and fresher product.

    Looking Ahead: Acetyl Chloride and a Changing Chemical Industry

    The pace of change in chemical manufacturing pushes those at the front lines to keep adapting. Acetyl chloride, with all its volatility and usefulness, sits at the intersection of demand for precision, safety, and speed. Up-and-coming chemists learn early how it can tighten a synthesis and deliver a purer product—the small moments when a successful transformation saves weeks of work.

    With sustainability climbing the agenda, the bigger question concerns whether new technological approaches can make acetyl chloride not just safer but greener. Some firms attempt bio-based production of related chemicals, but so far, most of the world’s supply remains petrochemical in origin. If one day a biomass feedstock reliably churns out acetyl chloride, entire segments of drug development and agrochemical production could see lower carbon footprints.

    Until then, the realities of production mean process engineers must design systems that keep emissions in check and waste streams responsible. This might mean tougher rules around fume scrubbing, or innovation in reagent recovery. Either way, the presence of acetyl chloride in these discussions speaks to its continuing power over how chemicals get made—and how people keep themselves, and the environment, safe in the process.

    Personal Perspective: Lessons From the Lab

    Having seen trainee chemists meet acetyl chloride for the first time, I remember the mix of nervous excitement and healthy respect. It doesn’t take many attempts before a person recognizes both the speed and the biting odor that flood the senses. Those early lessons stay with people, reminding them not to cut corners with PPE or ventilation.

    I’ve watched colleagues debate which acetylation route works best, calculating what’s on hand versus what can be ordered in on time—and always, acetyl chloride remains a reliable partner for quick, clean conversions. This experience underscores an industry truth: some chemicals, no matter their hazards, persist because their alternatives still can’t measure up.

    From a teaching perspective, acetyl chloride fosters conversations around balance and maturity in the chemical sciences. Its use connects students to a long lineage of experimenters and designers, from the first bench-top syntheses to the robotics-driven mini-reactors found in modern facilities.

    In Practice: Choosing and Using Acetyl Chloride Wisely

    Industry veterans often insist on blending older knowledge with new risk management strategies. For acetyl chloride, that means double-checking inventory controls, running annual safety drills, and backing up core processes with alternate routes—just in case a shipment falls through or a new regulation lands unexpectedly.

    More companies now publish transparency reports about how much acetyl chloride they use, and under what protocols. The push for public trust pushes handlers toward better record keeping and direct communication with surrounding communities. If a plant sits on the edge of a residential area, regular updates and open-door days calm nerves and build relationships.

    People building tomorrow’s supply chains won’t be able to ignore this compound. As demand for precision chemicals grows, acetyl chloride remains a bridge between raw materials and finished goods. Its reliable performance in acetylation brings predictability, while its hazards regularly sharpen the industry’s focus on safe design and strict oversight.

    Potential Solutions and Industry Shifts

    Reducing the risks tied to acetyl chloride doesn’t mean phasing it out, at least not yet. Instead, the field leans into:

    Through all of this, acetyl chloride endures as a linchpin in chemical synthesis. Those who work with it bear a responsibility not just to their process yields, but to safety and environmental stewardship. Every decision about scale, packaging, or method reflects a balance—reminding the industry that progress and caution must walk side by side.