2-Bromobutane: Chemistry, Safety, Application, and Future Outlook
Historical Development
Chemists in the late 19th century began exploring halogenated hydrocarbons, eager to expand what organic molecules could do in both the lab and industry. By the early 20th century, researchers tackled the challenge of synthesizing bromoalkanes like 2-bromobutane in bulk, since these compounds could unlock new routes in substitution reactions. The industrial culture of that time prized utility, leading to rapid integration of 2-bromobutane in chemical manufacturing. Over time, it showed its worth beyond academia, helping with improved reactions in pharmaceuticals and advanced materials. Synthetic efficiency improved through iterative trials, learning not just how to make more, but make it cleaner, with fewer impurities. This drive for purity set benchmarks in chemical engineering that still echo through every new batch made today.
Product Overview
2-Bromobutane belongs to a family of alkyl halides, finding important roles thanks to its four-carbon backbone and a single bromine atom attached to the second carbon. The position of bromine makes it chiral, introducing interesting applications in making enantiomerically pure products. With a molecular formula of C4H9Br and a decent market demand, companies stock this reagent across the globe for reliable substitution work. Its chemical reactivity arises not just from the presence of bromine, but also from the specific way it toggles between nucleophilic substitutions and eliminations. Labs and factories rely on 2-bromobutane's predictable outcomes: make an alcohol, tweak a pharmaceutical intermediate, or tailor a new solvent molecule. Flammability, volatility, and distinct odors remind anyone working with it that both opportunities and hazards walk hand in hand.
Physical & Chemical Properties
Pure 2-bromobutane forms a clear, colorless liquid. Pop the cap in any chemical storeroom, and a sweetish, somewhat sharp odor rises up. It boils at around 91-92°C, and it doesn’t hang out long in the cold, freezing at -112°C. Hydrophobic, it refuses to dissolve in water, yet mixes easily with ethanol, ether, and most organic solvents. Density lands at around 1.27 g/cm3, heavier than water—so in a spill, it slips below the surface. Its refractive index sits near 1.439, a number that matters to those measuring purity or setting up reaction monitoring tools. The bromine's bond to carbon makes the molecule reactive for many nucleophilic swapping games, and the secondary structure of the carbon increases selectivity in lab procedures.
Technical Specifications & Labeling
Commercial supply calls for technical accuracy, not mere promises. Purity levels usually exceed 98%, but pharmaceutical or fine chemical uses demand tighter control, sometimes as strict as 99.5%. Most suppliers list content of related impurities, water content below 0.1%, and freedom from hydrolysis byproducts. Labeling doesn’t just stop at names and grade. Strict international standards enforce GHS-compliant hazard symbols, signal words like “Danger”, directions for storage, and full indication of hazard classes. Batch numbers, manufacturer ID, and production dates guarantee traceability—every chemist wants to track issues down to a single container, not guess after an accident. This rigorous documentation builds trust in every bottle, ensuring not just performance but safety.
Preparation Method
Preparation usually follows classic organic teaching: start with 2-butanol and bring hydrobromic acid into play. Reaction between the alcohol and concentrated HBr works reliably, with heat nudging things along. Sometimes, sulfuric acid acts as a catalyst or co-reactant. Water acts as both a friend and foe—too much, and yield crashes. Laboratories often distill crude 2-bromobutane after synthesis to clear out side products. Industrial producers scale this method, using specialized reactors to fine-tune mixing, temperature, and separation. Some have adopted green chemistry tweaks, lowering waste and swapping out dangerous solvents where possible. The drive for cleaner production isn’t just environmental—it serves the bottom line, squeezing more product from each kilogram of starting material.
Chemical Reactions & Modifications
2-Bromobutane sparks creativity in any synthetic lab. The molecule’s secondary bromine lets it swing between SN1 and SN2 mechanisms, depending on reaction conditions. Add a strong nucleophile, and the bromine drops away, making room for sulfides, ethers, or substituted carboxylates. Swap the nucleophile, and different functional groups slip in, opening doors for new medicinal scaffolds or industrial additives. Under basic conditions, 2-bromobutane reacts via elimination, forming 2-butene—useful in polymer and specialty chemical synthesis. The molecule’s handedness, its chirality, leads to optical isomers, which matter in synthesizing single-enantiomer drugs. Chemists tweak conditions—temperature, solvent, reactant strength—to coax out a preferred product, minimizing unwanted side reactions that hurt yields.
Synonyms & Product Names
Different markets and generations know this molecule by distinct names. Besides 2-bromobutane, people in the field refer to it as sec-butyl bromide, 2-bromobutan, or even simply “butane bromide” in short-hand. Regulatory databases often record its CAS number for clarity: 78-76-2. With many companies branding their supply, proprietary trade names surface, but the major community trusts the basics. This diversity in naming sometimes causes confusion, but also reveals just how embedded 2-bromobutane has become in supply lines and chemical texts from different continents and decades.
Safety & Operational Standards
Direct experience working with halogenated hydrocarbons like 2-bromobutane warns every hand: handle with respect, or regret follows. Inhalation irritates lungs and throat, with dizziness or headaches showing up if exposure lasts. On the skin, it can burn or cause dermatitis. Liquid splashes threaten eyes, and the compound releases toxic fumes if burned or improperly disposed. Good labs always have PPE within arm’s reach—nitrile gloves, splash goggles, lab coats—and fume hoods running. Regulations from OSHA, REACH, and similar groups enforce safe use, setting permitted exposure limits and guiding spill response. Proper storage means cool, well-ventilated spots, far from open flames. Good transfer techniques and thorough training remain non-negotiable standards if workplace injuries are to stay rare.
Application Area
Real-world uses hook onto 2-bromobutane’s clean entry into substitution and elimination reactions. Pharmaceutical companies lean on it to build intermediates for antihistamines and pain relievers. Agrochemical labs turn to this molecule when crafting new pesticides or herbicide molecules. Organic synthesis courses use it as a teaching tool, showing students the clear fingerprints of SN2 and SN1 routes. Polymer research taps its potential for introducing reactive butyl groups into specialty plastics, giving them new flexibility or resistance properties. Some flavor and fragrance developers test 2-bromobutane-based compounds as starting points for aroma ingredients. The reach is wide not from hype, but from practical chemistry—if you want reliable control in forming carbon-heteroatom bonds, 2-bromobutane helps unlock it.
Research & Development
The frontiers of chemistry move with each new derivative or synthetic process emerging from R&D. Research groups keep probing 2-bromobutane’s structure, chasing enantiomerically pure forms through asymmetric synthesis, or developing catalysts that snatch the bromine away without dangerous byproducts. Pharmaceutical discovery teams experiment with new reactions based on secondary alkyl bromides to build more targeted drugs, and green chemistry advocates chase ways to make or break this molecule with lighter environmental footprints. A growing movement toward biocatalysis and mild conditions pushes for 2-bromobutane’s transformation using enzyme systems, showing the blend between organic tradition and biological innovation. These efforts don’t sit in journals—they spill over into new commercial opportunities, changing what industries can do next.
Toxicity Research
Toxicologists take 2-bromobutane’s effects seriously. Studies in animals and cellular assays have mapped out risks: respiratory irritation, central nervous system depression, and possible long-term organ impact at higher exposures. Absorption through skin or inhalation remains a key danger for workers. Chronic exposure correlates with liver and kidney changes in experimental models. Regulatory reviews inspect every data sheet, adjusting workplace exposure limits as toxicology catches up with new research. Waste handling and environmental release draw scrutiny, since even moderate concentrations could hurt aquatic life. For households, sale restrictions aim to keep this compound away from non-specialist hands, recognizing the gap in chemical literacy between a bench chemist and an average user.
Future Prospects
Future demand for 2-bromobutane won’t fade, but will face challenges—from regulatory pressure to develop safer alternatives, to the push for greener production methods. The molecule’s role in synthesizing chiral intermediates gives it a strong foothold, especially as drug and agrochemical makers chase more selective, less wasteful processes. Green chemistry will shape new routes, finding catalysts that work at room temperature, solvents that don’t pollute, and protocols that recycle waste streams. Digital chemistry tools, including machine learning and high-throughput screening, will sharpen our handle on its reactivity and open untapped synthetic shortcuts. Sustainable approaches and responsible use will likely dominate conversations, since a world striving for lower impact and higher safety can’t lean on toxicology blind spots or outdated lab habits. For young chemists facing today’s market, 2-bromobutane is less a relic—more a challenge to innovate better ways for tomorrow’s molecules.
Chemistry That Hits Home: 2-Bromobutane’s Formula Explained
2-Bromobutane brings back memories of working through those dense organic chemistry problems, staring down at a skeletal structure, and trying to make sense of the tiny symbols on the page. Some might have flinched at those chirality problems or reaction mechanisms. The good news? Figuring out the chemical formula doesn’t need to feel so intimidating.
Here’s the truth: the chemical formula for 2-Bromobutane is C4H9Br. With this, you have the basic count of carbons, hydrogens, and a single bromine. That’s all there is, and for a student or professional, recognizing what this formula represents makes all those classroom hours start to pay off.
How the Structure Matters
You might wonder why 2-Bromobutane specifically matters, as opposed to any other kind of bromobutane. Once you dig a bit deeper, the “2-” in its name reveals something interesting about its structure. This tells you that the bromine atom attaches to the second carbon in a straight chain of four carbons. The arrangement matters, not just to a chemist but for anyone who cares about how molecules react, smell, burn, or become fuel, solvent, or even a precursor to more interesting substances.
Bromine is not just any atom; it brings a specific set of chemical properties to the table, compared to, say, chlorine or iodine. The rest of the butane backbone provides the hydrocarbon skeleton, giving the compound its fundamental chemical behavior. Since most textbook reactions end up using compounds just like 2-Bromobutane, getting comfortable with its composition and formula will open doors, whether you’re studying nucleophilic substitution reactions or working in a lab trying to synthesize more complex molecules.
Down-to-Earth Importance
What difference does this formula make outside a classroom? In real work, knowing that formula means you can figure out the molar mass without trouble. C4H9Br gives you enough to quickly calculate how much of each element comes into play during a reaction or a synthesis. If you’re handling hazardous substances, recognizing this kind of formula helps you understand how volatile, reactive, or toxic a liquid might be. This is not just about passing an exam; it’s about safety, efficiency, and smart planning in any laboratory or industrial setting.
With an eye on E-E-A-T, keeping accuracy in scientific details helps everyone, from seasoned professionals to students who just stepped into their first organic lab. Real knowledge, grounded in reliable sources, means fewer mistakes and better science.
Addressing Mistakes and Improving Understanding
Missteps with chemical formulas can throw off an entire project or experiment. Ambiguity breeds confusion, so sticking to the proper formula helps keep everything on track. Suggesting a few memory tricks never hurts: visualize the butane chain, count your hydrogens, and add bromine to the right carbon. Drawing out the compound can make a world of difference, too. Sometimes, educators gloss over this, assuming everyone just “gets it”. But clarity saves time—and expensive reagents.
For those teaching or mentoring others, encouraging the next person to build molecules with models or sketches brings the subject to life. It sticks better than rote memorization. And for those learning on the job, slowing down to double-check that a compound matches the written formula keeps errors from snowballing into real-world hazards.
The Bottom Line
Knowing that 2-Bromobutane’s formula is C4H9Br turns what could seem like a jumble of letters and numbers into something concrete. Understanding the formula, the role of each atom, and the stakes in industry and education doesn’t just make you a better chemist. It reinforces the basic truth that clear foundations make advanced science stronger and more reliable.
Essential Building Block in Organic Synthesis
2-Bromobutane pops up often in discussion among chemists for a reason. Its structure, with a bromine atom attached to a butane backbone, makes it a straight shooter in substitution and elimination reactions. In my years of working with organic compounds, 2-Bromobutane always proved easy to handle and versatile, especially during undergraduate lab sessions. Its ease keeps beginners from making mistakes, and professionals appreciate how it speeds up reaction planning.
Many seasoned researchers reach for 2-Bromobutane when they want to introduce a butyl group into new molecules. Its carbon-bromine bond creates an active site that reacts reliably with a wide range of nucleophiles. This means someone working on pharmaceutical molecules, for example, can count on it when building more complex structures out of simpler pieces. Without reagents like this, labs need extra steps just to get the same result.
Practice Tool for Learning Stereochemistry
2-Bromobutane comes up in countless textbook problems for a reason. Its chiral center gives students a perfect chance to see how molecules can twist in space. It shows both the S and R forms, so you can experience the full picture of stereochemistry, not just read about it. I remember handling it in lab classes, knowing full well that the concepts behind it would come up in every exam. This experience transfers smoothly to real-world careers like drug development, where controlling the exact 3D shape of a molecule can make or break a drug's safety or effectiveness.
Link to Pharmaceuticals and Agrochemicals
Drug and pesticide makers need starting materials that can branch into dozens of directions. 2-Bromobutane serves as one of those waypoints. A chemical manufacturer aiming to produce specific butyl-based active ingredients uses 2-Bromobutane to kick things off. Many antihistamines, pain relievers, and crop-protecting agents contain fragments that come from this class of compounds.
The pharmaceutical industry, always on the lookout for efficient and cost-friendly paths, values reagents that leave as little waste behind as possible. 2-Bromobutane checks that box by reacting in a more predictable way compared to alternatives. Educators and researchers have published practical guides and reaction schemes featuring it, and you find evidence of this in journals covering drug discovery and agricultural chemistry.
Tools for Making New Polymers
Industrial chemists find 2-Bromobutane helpful in tweaking polymer properties. In the push to develop new plastics, rubber, or specialty materials, this compound works as an initiator in some polymerization techniques. You want a trigger to start a chain reaction, and the bromine atom makes that possible. The plastics developed using such methods appear in everything from some adhesives to insulation materials. The push toward recycling and safer plastics has increased interest in precisely the kinds of controlled chemistry that 2-Bromobutane helps make possible.
Laboratory Method Development and Industrial Scale-Up
Labs and pilot plants rely on easy-to-handle reagents for process development. 2-Bromobutane, thanks to its liquid state at room temperature, simplifies mixing and measuring. Its reliability shortens the time between experiment and successful pilot batch, helping companies cut costs and roll out products faster. Technicians and engineers often choose it for troubleshooting new synthetic pathways, especially in projects focused on building new production methods for specialty chemicals.
Responsible Handling and Health Considerations
No one should ignore the risks. 2-Bromobutane releases fumes that can irritate the eyes and lungs, so a good fume hood and gloves always belong in the setup. Regulatory groups recommend careful storage, clear labeling, and proper disposal. Over the years, training sessions in both academic and industrial settings emphasize this. Lab supervisors continually remind teams that even though 2-Bromobutane behaves predictably in reactions, safety always comes first.
Recognizing the Hazards
2-Bromobutane acts fast on the skin, eyes, and lungs. Even a small spill leaves a strong, sweet smell in the air and can irritate your throat. Some folks feel dizzy or light-headed after spending time around open bottles. Once, I knocked over a flask without gloves, and the stinging sensation on my wrist didn’t let up for hours. Skin contact isn’t just a quick annoyance — this compound soaks in, dries out tissues, and can lead to more serious issues like redness or even chemical burns after repeated exposure.
Inhaling its vapors over a period of time wears you down. Concentrated fumes cause coughing or choking, but even low levels take a toll. Exposure adds up if you’re careless with ventilation.
Personal Protective Equipment Actually Works
Splash goggles are a must, and not just to tick off a checklist. Regular safety glasses won’t stop a liquid like this from sneaking around the edges. I tried wearing contacts under my goggles once—never again. Tears stung, vision blurred, and I had to rinse out my eyes before getting back to work.
Gloves matter, too. Nitrile or neoprene work best. I hear students asking about latex—big mistake. Latex doesn’t offer enough resistance; the chemical seeps right through, unnoticed at first. Lab coats protect arms and clothes, but chemical aprons help when pouring larger amounts.
The Importance of Proper Ventilation
Fume hoods aren’t just for show. On days the hood fans failed, my throat got scratchy and the whole room felt thick. Poor airflow turns routine jobs into health hazards. Before lifting a flask, I always check the airflow with a strip of tissue to make sure suction still pulls.
Using open containers outside the hood causes trouble—spills become unavoidable, and fumes escape before you realize. Keeping 2-bromobutane capped and inside the hood until transfer reduces that risk by a mile.
Storage and Spill Response
This liquid reacts with strong bases and oxidizers, so I keep it far from cleaning supplies and other chemicals. Non-reactive containers with tight-fitting caps stay on lower shelves to limit damage if they fall. Once, a careless stack on an upper shelf sparked a spill that took hours to clean safely. I learned to check labels twice and avoid mixing storage with unfamiliar reagents.
Small spills clean up with absorbent pads, followed by a wash-down using detergent and water. Large spills should send people straight outside and alert a hazardous materials team. I remember one failed attempt to mop a puddle with paper towels—fumes hit fast and the towels didn’t absorb enough, spreading the liquid. The right gear and know-how made a real difference the next time.
Solutions That Build Good Habits
Proper labeling and keeping up-to-date safety data sheets within arm’s reach help new team members avoid confusion. Training goes further than just reading rules—a real walkthrough sticks better than lectures. New hires shadow someone who handles chemicals safely. Mistakes get fixed before they become habits.
Buddy systems, regular refresher courses, and drills keep safety procedures from fading into the background. Everyone looks out for each other this way. Good habits don’t start with fear; they grow out of experience and sharing what works.
Understanding the Boiling Point
2-Bromobutane boils at about 91 to 92°C under normal atmospheric pressure. Anyone who has ever worked in a college lab or even a high school science room has probably seen the fuss over measuring boiling points. For many, it sounds like a fussy detail, but knowing the precise boiling temperature of a chemical like 2-bromobutane makes a real difference. Distillation labs run smoothly only when you know exactly when your liquid will switch from bubbling gently to vaporizing away.
Why Does Boiling Point Matter in Chemistry?
During my time teaching organic labs, the boiling point was more than a number. It gave students a way to judge purity. Even a few degrees out of range warned us that our 2-bromobutane was mixed up with something else, maybe leftover solvent or water. Experienced chemists and industry workers use these numbers almost daily, since you can’t separate or purify chemicals on a larger scale without understanding these properties first.
There is another piece to this. Safety. Working with flammable or volatile chemicals, people can’t afford to take boiling points lightly. 2-bromobutane sits near the lower end for organic solvents. Leave an open bottle too close to a heat source, and the stuff can start evaporating. In a badly ventilated place, inhaling vapors causes headaches, or worse. Knowing the exact boiling temperature helps us pick the right gear and set up the right extraction or distillation.
What Makes 2-Bromobutane’s Boiling Point Unique?
Chemists look at 2-bromobutane alongside similar types of molecules, like 2-chlorobutane or 1-bromobutane. Replace the bromine atom with a different halogen, or switch the bromine to a different position, and the temperature goes up or down. Heavier atoms like bromine pull up the boiling point due to stronger London dispersion forces, so 2-bromobutane boils higher than its chloro cousin. Hands-on experience shows that these differences make the backbone of chemical separation. Even pharma companies lean hard on these principles while they refine active ingredients from reaction broths.
Industry Relies on Precision
Look at manufacturers scaling up a chemical process. They need repeatable, precise numbers for each batch. Even a few degrees too high or low can mean product loss or contamination. Poor control means wasted time, money, and raw material. Someone running a pilot plant distillation or trying to optimize energy use won’t trust a ballpark number—they need data measured to the degree. That’s why databases, handbooks, and safety sheets go through so much double checking before printing a boiling point.
Improving Data Quality
Data-sharing networks and digital lab notebooks are making it easier to report up-to-date physical properties. Real-world chemists crowd-source problems and fix errors by sending feedback to journals and chemical suppliers when published boiling points don’t line up with results. Some research groups turn to advanced techniques, like differential scanning calorimetry, to sharpen accuracy. Traceable, transparent methods will keep science moving forward.
Reliable Knowledge Serves More Than Labs
Science thrives on solid information. In my own time mentoring younger students, it’s clear that learning to trust—not just memorize—numbers like the boiling point of 2-bromobutane makes the transition from classroom to professional lab easier. By teaching people to double check, record, and use physical properties thoughtfully, we’re building not just better chemists, but safer, more efficient workplaces.
Understanding the Risks and Why Storage Matters
2-Bromobutane turns up in a lot of college organic chemistry labs and some industrial setups. At a glance, it looks harmless—clear and nearly odorless. But even small mistakes in storage can lead to headaches nobody wants, from damaged glassware to real safety emergencies. People sometimes treat smaller bottles as less risky than big drums, yet mishandling either can mean trouble. This is one of those chemicals best treated with a mix of respect and practicality.
Immediate Hazards of 2-Bromobutane
Spilling this stuff stings nostrils. Let it sit uncapped, and the fumes crawl around the room. Volatile organic compounds like 2-Bromobutane irritate skin and can spark headaches or nausea after breathing fumes. It catches fire if splashed near heat or open flames. The liquid also reacts with strong bases and some oxidizing agents, so keeping it away from bleach or strong cleaners means fewer risks.
Temperature and Light Concerns
I’ve seen more than one bottle start to cloud up or turn yellowish because someone stashed it near a sunny window. Light and temperature swings mess with its stability, which can add impurities and cause leaks. A storage space with room temperature, low light, and good ventilation helps a lot here. In a pinch, a standard flammable storage cabinet fits the bill. A dedicated fridge is overkill unless dealing with huge volumes, but hot rooms or direct sunlight never help this chemical keep its shelf life.
Container Choices: Original Packaging Pays Off
The manufacturer’s bottle earns its price. Sturdy glass or certain types of high-quality plastic seal tight and resist breakdown. 2-Bromobutane loves to work its way through low-grade plastics, which means thin-walled containers can leak or even break. Replacing broken containers invites spills and exposure, so sticking with the original is safer and saves trouble later. Screw caps should close firmly every time. Metal screw tops or corks cause rust and leaks, so those habits don’t help anyone.
Ventilation and Fire Safety
Even in small labs, a simple fume hood pulled down tight stops vapors from moving around. Working next to an open window or fan reduces the chance of breathing in fumes. Class B fire extinguishers and a spill kit within reach pay off if something goes wrong. Cotton lab coats or sturdy chemical aprons and gloves cut down on accidental splashes—even one dribble on uncovered skin causes a burning sensation.
Segregating Incompatible Chemicals
Every bottle ought to sit in a labeled, segregated spot far from acids, strong bases, or oxidizers. I once watched a rookie shove all reagents onto one shelf, then curse weeks later after a small bottle developed pressure and popped its seal. Stack flammables together, with clear dividers if possible, and label them so no one grabs the wrong material. Even seasoned lab workers run through their inventory every month to check for leaks, missing labels, or old containers past their expiration dates. This simple habit has saved me from cleaning up sticky, hazardous messes more than once.
Waste and Cleanup Practices
Extra or old material goes in a sealed, labeled waste bottle, never down the sink. Plenty of people make the sink mistake, then find themselves on the phone with the hazardous materials response team. Neutralize sap spills with absorbent pads meant for organics, then toss everything in a hazardous waste bin. Clean surfaces with isopropanol or plenty of soapy water, tossing dirty towels straight into the waste container.
Safer Storage Means Fewer Problems Down the Line
Simple moves protect people and property. Store 2-Bromobutane out of sunlight, seal containers tight, keep it distant from incompatible chemicals, and review inventory regularly. These practices prevent injuries and cut the risk of environmental contamination. Following clear labeling and good ventilation lowers exposure without fancy gear. The best labs build habits that make safe storage routine, not a guessing game every time someone grabs a bottle off the shelf.


| Names | |
| Preferred IUPAC name | 2-Bromobutane |
| Other names |
sec-Butyl bromide
sec-Butane bromide 2-Butyl bromide Butan-2-yl bromide |
| Pronunciation | /tuːˈbroʊ.moʊ.bjuːˌteɪn/ |
| Identifiers | |
| CAS Number | 78-76-2 |
| Beilstein Reference | 1718731 |
| ChEBI | CHEBI:35686 |
| ChEMBL | CHEMBL153998 |
| ChemSpider | 68295 |
| DrugBank | DB02029 |
| ECHA InfoCard | ECHA InfoCard: 100.004.215 |
| EC Number | 205-118-3 |
| Gmelin Reference | 786 |
| KEGG | C01561 |
| MeSH | D001943 |
| PubChem CID | 6560 |
| RTECS number | EJ9835000 |
| UNII | T4K0R13F0Y |
| UN number | UN2349 |
| CompTox Dashboard (EPA) | `DTXSID5020676` |
| Properties | |
| Chemical formula | C4H9Br |
| Molar mass | 137.02 g/mol |
| Appearance | Colorless liquid |
| Odor | sweet odor |
| Density | 1.262 g/mL at 25 °C (lit.) |
| Solubility in water | Slightly soluble |
| log P | 1.98 |
| Vapor pressure | 3.12 kPa (at 20 °C) |
| Acidity (pKa) | 47 |
| Basicity (pKb) | 2.69 |
| Magnetic susceptibility (χ) | -73.0×10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.437 |
| Viscosity | 0.49 cP (20°C) |
| Dipole moment | 2.00 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | (329.6 J·mol⁻¹·K⁻¹) |
| Std enthalpy of formation (ΔfH⦵298) | -81.2 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -2470.7 kJ/mol |
| Hazards | |
| GHS labelling | GHS02, GHS07 |
| Pictograms | GHS02,GHS07 |
| Signal word | Warning |
| Hazard statements | H225, H315, H319, H335 |
| Precautionary statements | P210, P233, P240, P241, P242, P243, P261, P271, P301+P312, P303+P361+P353, P304+P340, P305+P351+P338, P312, P331, P370+P378, P403+P235, P501 |
| NFPA 704 (fire diamond) | 1-2-0 |
| Flash point | 10 °C |
| Autoignition temperature | 180 °C |
| Explosive limits | 1.6–8.4% |
| Lethal dose or concentration | LD50 oral rat 2730 mg/kg |
| LD50 (median dose) | LD50 (median dose): Oral rat 2730 mg/kg |
| NIOSH | KW0085000 |
| PEL (Permissible) | PEL: 100 ppm |
| REL (Recommended) | 200 ppm |
| IDLH (Immediate danger) | 800 ppm |
| Related compounds | |
| Related compounds |
Butane
1-Bromobutane 2-Chlorobutane 2-Iodobutane sec-Butyl alcohol |