Acetonitrile’s journey traces back to the late 19th century, surfacing as a simple byproduct in the production of acrylonitrile. In those early years, nobody paid much attention to those faint, clear streams of acetonitrile dripping off the end of the distillation column. Chemical producers locked their sights on their primary products, tossing aside this side-stream solvent most years. Over time, researchers started noticing its unique qualities. The rise of modern analytical chemistry during the 1950s drove up demand for higher purity reagents that wouldn’t ruin sensitive chromatography columns. Synthetic chemists, solvent manufacturers, and the pharmaceutical sector started to see the opportunity hidden in those neglected barrels. Eventually, acetonitrile earned a central spot in so many applications—from the toolkit of every analytical lab to the batch reactors making heart medications.
Acetonitrile, known commonly as MeCN, is one of the most versatile, small organic nitriles out there. Its physical form offers a colorless liquid, easy to pour and measure, and it brings that familiar, mild sweet-ether smell into the lab. It’s classified under the nitrile family, packing a cyano group on a two-carbon chain. Despite that intimidating functional group, acetonitrile rarely causes handling headaches for experienced chemists—if the right procedures stay in place. The worldwide production stands around one hundred thousand tons per year, serving as a crucial intermediate for various organic syntheses. People who work with HPLC, battery electrolytes, DNA synthesis, or pharmaceutical extractions recognize this solvent right away. Whether on a flammable liquid drum in an industrial warehouse or a small brown bottle in a research lab’s fridge, acetonitrile’s footprint spans several fields and continents.
Acetonitrile stands out because of its modest boiling point (82 °C), low viscosity, and polar aprotic nature. It mixes well with water, methanol, and most organics, but keeps itself distinct from ethers and nonpolar hydrocarbons. The density holds at about 0.786 g/cm³. Its dielectric constant (approx. 36) makes it an excellent solvent for ions—a big reason it powers HPLC. Electricians and materials scientists value its low freezing point, so winter temperatures rarely slow down its storage or transfer. Acetonitrile resists oxidation under typical lab conditions. Its small size and reactivity let it dissolve polar and non-polar compounds, making it the workhorse for gradient elution in liquid chromatography.
High-purity acetonitrile for HPLC or LC-MS finds itself labeled with UV absorbance parameters, moisture content (as low as 0.05% sometimes), and detailed trace impurity profiles. The product packaging usually features GHS-labeled warnings: “Flammable liquid and vapor,” along with standardized pictograms. Every reputable supplier lists the CAS number (75-05-8), and regulatory compliance with REACH or TSCA usually appears in the fine print. Shipping requirements typically demand UN 1648 classification, amber bottles, and vapor-tight seals to keep light and air away from the product. Technical data sheets usually spell out acidity or alkalinity levels, color index, and residue after evaporation—essential for analysts and manufacturers who can’t afford clogged columns or contaminated batches.
Most acetonitrile produced worldwide comes as a side stream from the commercial production of acrylonitrile via the Sohio process. Propylene, ammonia, and oxygen flow through a fluid-bed reactor, and amid all the complex organic reactions inside, acetonitrile forms in lower concentrations. Afterward, careful distillation or extraction pulls acetonitrile away from a complex chemical soup. Lab-scale techniques, though less common, treat acetamide or ethyl alcohol with dehydrating agents or oxidation catalysts to isolate small batches of MeCN. Few other means rival the cost efficiency of large-scale petrochemical byproduct recovery, so this remains the dominant industrial strategy.
Acetonitrile’s simple structure hides a surprising chemistry. Strong bases attack the methyl group, making it a useful precursor for nucleophilic substitutions or alkylation reactions. Deprotonation forms the acetonitrile anion, which serves as a building block for synthesizing specialty fine chemicals. Photochemical and electrochemical researchers use MeCN as a solvent because its high electrochemical window resists breakdown, allowing them to study redox-active species. Some routes convert acetonitrile to ethylamine (a crop and chemical staple) or hydrolyze it to acetic acid and ammonia under harsh acidic or basic conditions. In peptide coupling reactions, acetonitrile acts as both solvent and facilitator, demonstrating how an unassuming molecule finds itself at the crossroads of modern synthesis.
A chemist’s lexicon throws several names around, depending on the audience: methyl cyanide, ethanenitrile, cyanomethane, or MeCN among them. In the bulk chemicals world, the short “ACN” label often appears on shipping documents and safety datasheets. Some standardized product names in the chromatographer’s toolbox include “HPLC grade acetonitrile” or “MS-grade acetonitrile,” signaling fitted-for-purpose purity and filtration. Scientific suppliers might tag it under numbers denoting water content or micrograms-per-liter residual metals, catering to precision work in genomics or proteomics.
Working with acetonitrile safely depends on a proper respect for its flammability, volatility, and moderate toxicity. Anyone in a lab or plant should always know the risk of quick ignition—static electricity or sparks around open containers invite disaster. Ventilated hoods, safety goggles, chemical gloves, and knowledge of the emergency eyewash location rise to the top of any training. Inhalation brings nausea or headaches, while large skin exposures cause dryness and even cyanide-like toxic effects under chronic conditions. Late 20th-century accidents taught safety teams the perils of confined spaces and improper waste disposal. International standards keep evolving. OSHA, ACGIH, and ECHA regularly update exposure limits, demanding routine air monitoring and strict waste segregation to keep environmental releases away from groundwater.
Modern chemical labs and factories reach for acetonitrile across a wild variety of tasks. HPLC chemists rarely scan their shelves without spotting several bottles; the solvent’s low viscosity and high polarity support precise separations of pharmaceuticals and natural products. Extractive chemists turn to MeCN for pulling alkaloids or peptides from plant sources and fermentation broths. Lithium-ion battery manufacturers need acetonitrile-based electrolytes for improved cycling and reduced flammability. Organic synthesis experts value MeCN for its stability and ability to dissolve reagent salts and Lewis acids. Environmental researchers analyze pollutants and toxins in food or water supplies using acetonitrile-based sample prep. Even the DNA world depends on acetonitrile during automated solid-phase oligonucleotide synthesis because it cleanly supports coupling and deprotection steps. Every field develops its own shorthand for working with this small, quiet molecule, but the shared value lies in its clarity, miscibility, and reactivity.
A constant stream of research writes the next chapters in acetonitrile’s story. Analytical chemists keep looking for new stationary phases and mobile phase combinations that pair with acetonitrile to tackle tougher separations or faster analyses. Electrochemists deploy acetonitrile as a test-bed for new redox mediators and battery solvents. Synthetic chemists search for ways to functionalize acetonitrile’s simple scaffold into complex building blocks, while pharmaceutical process teams engineer greener recovery modes to reduce production waste. In recent years, efforts ramped up to “recycle” acetonitrile from spent solvents, driven by sudden shortages and market swings from the acrylonitrile sector. Intellectual property filings point toward novel catalysts or process intensification schemes that lower byproduct loads and boost purity.
Acetonitrile hits both sides of the coin: relatively benign in small quantities but carrying serious hazards with careless use. Toxicologists investigated its metabolism in the body, finding it converts to hydrogen cyanide, especially if exposure gets out of hand. Workers exposed to chronic low doses sometimes show subtle neurological or gastrointestinal complaints. High acute doses lead to confusion, seizures, and, in rare cases, fatal respiratory failure. Animal studies helped establish occupational exposure limits—typically 40 ppm for an 8-hour shift—balancing industrial possibilities with basic human safety. Occupational health scientists urge ongoing monitoring and improved detection technology, since early symptoms of overexposure resemble headaches or flu, causing some early cases to slip by unnoticed. Environmental fate studies note that acetonitrile breaks down under sunlight and microbial action, but high local spills could disrupt aquatic systems until full breakdown finishes. These insights keep regulators watchful and safety trainers on their toes.
Looking forward, acetonitrile stands at the center of several growing fields. The rise of genomics and personalized medicine drives the need for even purer, ultra-low residue solvents for DNA sequencing. Battery researchers dig into acetonitrile for next-generation electrolyte formulas supporting longer-range electric cars. HPLC method developers hope new solvent recycling approaches will cut down on environmental waste and cost—two factors getting more attention each budgeting season. Some companies investigate direct synthetic processes from renewable precursors, hoping to break acetonitrile’s dependence on the fluctuating acrylonitrile market. Regulators worldwide focus on exposures and spilled volumes, pushing for automated containment and remote vapor monitoring systems. Each year, the circle widens: more fields, tighter guidelines, smarter use. Acetonitrile may not headline the glossy covers of science magazines, but daily, it powers breakthroughs in pharmaceuticals, environmental control, and materials chemistry—quietly holding its place as both a legacy chemical and a future staple.
Every time someone in a lab runs a high-performance liquid chromatography (HPLC) test, there’s a good chance acetonitrile does the heavy lifting. Chemists pick it not just for its clear appearance but for how easily it mixes with water and organic solvents. The value of acetonitrile became clear to me working in an analytical lab. Choosing the right solvent saves several hours of troubleshooting, especially in pharmaceutical analysis, where results often decide a drug’s safety. MeCN’s ability to resolve complex mixtures has helped deliver countless clinical breakthroughs.
Besides helping labs break down drug ingredients and impurities, acetonitrile also serves as a starting material in pharmaceutical synthesis. It ends up shaping core parts of medications, building molecules for antidepressants and antibiotics. While the chemical might not grab headlines, its absence would hold back the development of new therapies. Pharmaceuticals depend on trusted materials, and tight global supply—like during the 2008 shortage—forced some companies to delay critical health projects. It’s a reminder that even supporting chemicals behind the scenes can shape what’s possible in public health.
Not all of acetonitrile’s value shows up in medicine. The electronics industry counts on exceptionally pure chemicals, and MeCN stands out here, too. It finds its way into the production of lithium batteries as an electrolyte component, helping energy move efficiently between components. Cleaner energy storage depends on materials science, and any improvement here means longer lifespans for batteries in our everyday devices. As electric vehicles gain ground, finding reliable sources of quality solvents like MeCN will help shape the pace of change on city streets.
Environmental labs rely on acetonitrile to pull pesticides and toxins out of food, soil, and water samples. In food safety, the QuEChERS (Quick, Easy, Cheap, Effective, Rugged, and Safe) method uses this solvent to extract residues from fruits and vegetables. It streamlines analysis, makes food safer, and opens doors for better regulations. My own time working with agricultural products showed how solvent quality changes results—you know a chemical’s impact by how many recall crises it quietly helps avert.
Acetonitrile’s evaporation rate and low toxicity, compared to similar compounds, give it more versatility. It also supports dye and perfume industries, fitting into processes where purity and reaction speed matter. It doesn’t just keep businesses moving; the right chemical helps regulators check what ends up in the market.
In recent years, securing enough acetonitrile has turned tricky. Most of the world’s supply comes as a byproduct from making acrylonitrile, a key material in plastics. That means shifts in plastic demand hit solvent users hard. The aftermath of refinery shutdowns or dips in plastic production, as seen in 2008, ripple out to lab benches and manufacturing floors everywhere.
Handling acetonitrile safely is as important as using it efficiently. Accidental spills risk health and environmental harm. Routine exposure checks, good training, and tighter regulations offer a safety net. Some companies look for ways to recycle spent solvent, reducing both costs and emissions, but that works best when governments support cleaner technologies.
Securing consistent, high-quality supply will call for investment in alternative production routes and better recycling. Shared responsibility—between industry, regulators, and researchers—keeps acetonitrile both useful and safe, preserving its role in progress across science, medicine, and sustainability.
Acetonitrile has become a staple in chemistry labs, often finding its way into analytical work, pharmaceutical research, and even some electronics manufacturing. Sitting in a clear glass bottle, it looks harmless—almost like water. That’s where many mistakes start. Acetonitrile doesn’t announce its dangers. Many of us once figured a chemical in daily use couldn’t cause too much trouble, but experience changes that outlook.
The smallest lapse in real safety practices can have real consequences. Just a splash on a gloved hand or a forgotten open bottle reminds you of its toxic vapor and its flammability. It’s lighter than water but its effects hit hard and fast.
After working in both young and established labs, one pattern stands out: ventilation makes a difference. Even without strong smells, acetonitrile lets off vapors you can’t always sense right away. Fume hoods aren't an unnecessary expense—they protect lungs and keep headaches and dizziness out of your day. Skipping proper airflow sometimes seems easier, especially if a quick process gets rushed. That shortcut usually leads straight to health complaints and sometimes ER trips for the unlucky.
Acetonitrile doesn’t need much to light up. A spark, a loose hotplate, or a static discharge can start trouble. I’ve seen spill kits disappear just when they’re needed most. Fire extinguishers and spill control tools belong within arm’s reach, never stashed in a back closet. Only keep the minimum quantity on the bench. Store the rest in a well-marked, flame-proof cabinet with a tight seal.
An unlabeled bottle creates confusion and risk. Every container deserves a clear, waterproof label with name and hazard warnings—no shortcuts or scribbles. Acetonitrile breaks down over time in sunlight or near heat sources, releasing toxic gases. Keep all supplies in a cool, shaded chemical storage area. Where I worked, one careless placement next to a radiator led to a cleanout and some stern words from safety officers.
Lab coats only go so far. Those handling acetonitrile require splash-resistant goggles, gloves made of nitrile or neoprene, and closed shoes. I learned early that latex gloves don’t stand up to this solvent; switch to proper material or waste time and risk burns. Contamination sneaks onto hands, sleeves, and work surfaces. Frequent glove changes and surface wipes cut down on mistakes.
Experience grows with every shift, but honest training saves more headaches. No new team member ever regrets an extra walk-through of chemical hygiene plans. Regular emergency drills, eyewash station checks, and up-to-date safety data sheets matter more than most people expect—until something goes wrong.
Mistakes happen. Most stories start with a forgotten bottle or a late-night rush. Building a culture where anyone can call out a storage problem—without getting brushed off—protects both newcomers and veterans. Fast response and honest conversations prevent accidents from turning into disasters. It’s not about paranoia. It’s about respect for every person working with or near these bottles. Acetonitrile’s just one bottle among thousands, but it’s never just another clear liquid.
Acetonitrile often pops up in labs, factories, and even classroom experiments. Most people know it as a common solvent, but the shorthand that scientists trust every day is its chemical formula: CH3CN. This simple combination of carbon, hydrogen, and nitrogen speaks volumes about what this compound can do. If you’ve ever wondered why the formula is so important, think of it as the compound’s unique fingerprint. No other chemical lines up its atoms in the same way, so the formula tells chemists exactly what they are dealing with, no guesswork.
Every chemical gets a unique number from the Chemical Abstracts Service, called a CAS number. Acetonitrile’s is 75-05-8. This isn’t some arbitrary code for databases. In my work in a university chemistry storeroom, labeling every bottle correctly with a CAS number meant mistakes could get weeded out before they turned dangerous. If you pull a bottle from a shelf and see that number, you know precisely what’s inside, no matter what language you speak or who packaged it. In a global supply chain, those digits keep chemicals moving safely and legally across borders.
Acetonitrile doesn’t grab headlines like some industrial chemicals, yet it’s crucial in fields from pharmaceuticals to environmental testing. Labs use its unique properties for thin-layer and gas chromatography, helping analysts spot contaminants at extremely low levels. Getting the chemical formula and CAS number wrong could throw off readings, or worse, lead to unsafe mixtures. Years ago, a colleague recounted how a shipment with a mismatched label nearly led to dangerously hot reactions in their plant. The right formula and number helped spot the error before a bad mix happened, saving time, money, and maybe a life.
More imported chemicals flow through ports and warehouses than ever before. Regulators and customs officials lean heavily on CAS numbers. When a shipment arrives for quality control testing, the inspectors look up the CAS number to double-check regulations for that exact substance. If counterfeiters try sneaking in hazardous or inferior materials, mislabeling is a tool of the trade. What helps authorities sort the wheat from the chaff is a correct, verifiable identifier right on the label.
One straightforward improvement would be insisting on electronic registries that connect CAS numbers to shipment records and usage logs, accessible worldwide. Barcode labels and QR codes tied to chemical inventory systems help trace products from source to user. Old habits, like jotting down common names instead of standardized numbers, bring unwanted risk. Encouraging strict record-keeping and training workers to cross-check CAS numbers will prevent costly mix-ups and boost end-user safety.
In the end, the chemical formula CH3CN and the CAS number 75-05-8 are more than just technical jargon. They protect workers, consumers, and even the environment by giving everyone a single, reliable reference point. Whether you’re a chemist running a test, an importer processing a shipment, or a teacher explaining chemical safety, these identifiers help keep science honest and people safe.
Acetonitrile doesn’t make the headlines the way household names like bleach or ammonia do. But step inside a lab or some chemical plants and its smell is hard to miss. It dissolves stuff that water cannot, shows up as a byproduct during acrylonitrile production, and gets loads of use in fields like pharmaceuticals and plastics manufacturing. I’ve watched chemistry students pull out bottles of the clear, sharp-smelling solvent like it’s a harmless tool. Few realize how much risk hides in that little glass container.
Breathe some acetonitrile in, and your throat might feel scratchy, maybe your eyes water. But the real danger kicks in with repeated or heavy exposure. Short-term contact makes folks dizzy, brings out headaches, or irritates the skin. The bigger worry: inside the body, enzymes convert acetonitrile into cyanide—yes, the same poison tied to infamous historical cases. This means long-term or large exposures can kill. Smaller, repeated amounts? They might not bring on symptoms right away, but damage can build, hurting organs and affecting the nervous system.
Years back, I saw a colleague spill some on his arm. He brushed it off, figuring ‘just another chemical.’ The rash and nausea that followed changed his mind for good. There’s no overplaying it: Personal protective equipment isn’t optional here, and anyone handling this chemical in regular settings needs real training, not just a safety sheet signed at orientation.
Acetonitrile doesn’t stay put. Once dumped down drains or vented to the air, it ends up in water, soil, and the atmosphere. The stuff evaporates quickly, so it won’t usually build up in groundwater. Still, fast evaporation just means it spreads differently. In rivers and lakes, even low concentrations stress aquatic life. Fish and bugs won’t always die on the spot, but studies show effects on growth, reproduction, and long-term survival.
I spoke with a local water board technician who said treatment plants are only partly effective against chemicals like this. Some always slip through, so communities relying on surface water can end up with trace amounts in the taps. Over time, low doses in the environment creep up the food chain. Nobody invited this chemical to dinner, but it finds a way.
Common sense says handling acetonitrile demands respect. Stick to certified hood systems, wear gloves and goggles, and train workers with real-life scenarios, not just paper tests. If a spill happens, treat it like the genuine emergency it is—evacuate, ventilate, neutralize, then collect residues as hazardous waste.
Companies can limit risk with better closed-system technology and by switching to solvents with fewer health effects when possible. Regulators like the EPA and OSHA set exposure limits, but rules need teeth. Citizens should have access to transparent data about local emissions and water testing results. Industry pressures often fight stricter regulation, citing costs, but the public bears the long-term health bills when safety corners get cut.
Acetonitrile’s dangers don’t mean fleeing from chemistry or progress. They mean taking responsibility in every part of the chain—from manufacturing to disposal. People’s health and natural ecosystems weigh more than speed or cost savings in any lab or factory ledger.
Anyone who’s spent time in a lab or factory sees how chemical packaging isn’t just about convenience—it’s about regulation, safety, and making the budget work. Acetonitrile, for example, has earned its place as a tough but versatile solvent. Between chromatographers who need pure solvent for HPLC and chemical manufacturers running larger-scale reactions, there’s no single-size solution.
The most common bottle you’ll spot on an analyst’s bench is the one-liter amber glass. Manufacturers, including Sigma-Aldrich, Thermo Fisher, and Honeywell, stick to this size because it lines up with daily routine and proven safe handling for volatile solvents. You get enough for dozens of sample runs without tying up too much money on the shelf. That classic glass bottle also cuts down on potential leaching and keeps light-sensitive chemicals in decent shape.
Move up to the four-liter or gallon jug and you hit the sweet spot for high-throughput workflows, like sample prep or method development. This size still handles pretty well, but now the cost per liter drops. From my own experience, when you’re running a project with lots of method scouting or sample extraction, these big bottles keep things moving without deals with frequent reordering.
There’s also a real demand for 2.5-liter glass or HDPE (high-density polyethylene) bottles. Some vendors gear their products toward customers with middle-range usage. Think of small research groups, or diagnostic companies who need a buffer between stock issues and space constraints.
Once production scales really expand, companies start looking beyond the bench sizes. Factories may bring in 20-liter, 25-liter, or even 200-liter (drum-sized) options. These containers, made of strong HDPE or stainless steel, cut down on packaging waste and lower shipping costs per unit. Bulk packaging works well where whole departments or companies depend on acetonitrile for daily processes, for instance in pharmaceutical synthesis or large-scale purification.
With these bulk sizes comes extra responsibility. One spill can turn hazardous fast. Secure closures, pressure relief valves, and certified containers are not optional. Regulatory pressure—from GHS labeling, EPA tracking to proper secondary containment—keeps teams focused on safety and compliance. In the field, nobody hesitates to spend more for packaging that’s fully traceable, batch-stamped, and tamperproof. This focus comes from learned lessons; in my early days, a leaky carboy once created a massive headache, wasted product, and left a lingering tang of solvent in the storage area for weeks after cleanup.
Quality control doesn’t end at the manufacturer. Even after arrival, users must check seals, inspect for cracks, and store containers away from heat or flame. HDPE stands up better in rough environments but can’t match glass for solvent purity. Many warehouses use both options, adjusting their choice according to budget, safety audits, and solvent-grade requirements.
Environmental rules have changed the calculation. Single-use glass once dominated, but recycling efforts—along with pressure to cut hazardous waste—push organizations toward returnable totes, safe-drain systems, and pooling purchases for fewer shipments. Companies ready to meet these standards score points with customers and supply partners alike.
Experienced buyers keep an eye on storage, handling training, and how well packaging matches use rates. By choosing the right size—ranging from small glass bottles for precision work up to industrial drums for manufacturing—organizations get more value, safety, and regulatory peace of mind out of each order.
Names | |
Preferred IUPAC name | Ethanenitrile |
Other names |
Cyanomethane
Methyl cyanide Ethanenitrile Methylnitrile MeCN |
Pronunciation | /əˌsiːtəˈnaɪtraɪl/ |
Identifiers | |
CAS Number | 75-05-8 |
Beilstein Reference | 60714 |
ChEBI | CHEBI:38438 |
ChEMBL | CHEMBL12537 |
ChemSpider | 7338 |
DrugBank | DB13128 |
ECHA InfoCard | 03b9eea5-6d72-4b60-9b6a-4fd74e7a1e6b |
EC Number | 200-835-2 |
Gmelin Reference | 63511 |
KEGG | C01380 |
MeSH | D000223 |
PubChem CID | 6342 |
RTECS number | AL7700000 |
UNII | 3G5A0D9I8A |
UN number | 1094 |
Properties | |
Chemical formula | C2H3N |
Molar mass | 41.05 g/mol |
Appearance | Colorless transparent liquid |
Odor | Ethereal |
Density | 0.786 g/cm³ |
Solubility in water | miscible |
log P | -0.34 |
Vapor pressure | 84 mmHg (20°C) |
Acidity (pKa) | 25 |
Basicity (pKb) | -10.6 |
Magnetic susceptibility (χ) | -10.2×10⁻⁶ cm³/mol |
Refractive index (nD) | 1.344 |
Viscosity | 0.37 mPa·s (at 25°C) |
Dipole moment | 3.92 D |
Thermochemistry | |
Std molar entropy (S⦵298) | 160.7 J·mol⁻¹·K⁻¹ |
Std enthalpy of formation (ΔfH⦵298) | ΔfH⦵298 = +75.0 kJ/mol |
Std enthalpy of combustion (ΔcH⦵298) | -333.6 kJ·mol⁻¹ |
Pharmacology | |
ATC code | Acetonitrile does not have an ATC code |
Hazards | |
GHS labelling | GHS02, GHS07 |
Pictograms | GHS02,GHS07 |
Signal word | Danger |
Precautionary statements | P210, P261, P273, P280, P301+P310, P303+P361+P353, P304+P340, P311, P312, P330, P337+P313, P370+P378, P403+P233, P501 |
NFPA 704 (fire diamond) | 2-3-0 |
Flash point | 6 °C |
Autoignition temperature | 525 °C |
Explosive limits | Explosive limits: 4.4%–16% (in air) |
Lethal dose or concentration | LD50 Oral Rat: 2730 mg/kg |
LD50 (median dose) | LD50 (median dose): 2730 mg/kg (oral, rat) |
NIOSH | K048 |
PEL (Permissible) | 40 ppm |
REL (Recommended) | 1-5 ppm |
IDLH (Immediate danger) | IDHL: 200 ppm |
Related compounds | |
Related compounds |
Acetone
Acetamide Acetic acid Acetaldehyde Propionitrile |