2-Bromopropane: A Close Look at Its Role in Modern Chemistry
Historical Development
Chemistry stands on the shoulders of its pioneers, and 2-bromopropane offers an example of quiet persistence rather than front-page drama. Early references to organobromine compounds pop up in journals from the late 19th and early 20th centuries. Laboratories in Europe and North America learned how to coax halogens onto hydrocarbon scaffolds, but only through cautious trial and error. By the 1950s and 1960s, chemists handled small molecule halides such as 2-bromopropane with routine confidence. This compound stands as a testament to iterative development: only with better purification techniques, gas–liquid chromatography, and reliable supply could brominated propanes leave the bench and serve larger ambitions in synthesis and manufacturing.
Product Overview
2-Bromopropane, or isopropyl bromide, carries the formula C3H7Br. On the surface: it’s a colorless, volatile liquid with a slight sweet odor. Beneath this calm presence, it stashes a feisty bromine atom, ready to jump into molecular swaps. Industrial suppliers offer it as a staple for small-scale application and research—each bottle sealed against moisture, as trace water can degrade its value. It’s not just a random halide. Organic chemists keep it on hand for its direct utility in synthesis, especially for producing branched intermediates and exploring substitution versus elimination reactions.
Physical & Chemical Properties
The boiling point hovers near 59°C, which makes 2-bromopropane easy to distill and separate from less volatile impurities. Its density ranges around 1.31 g/cm3, packing more weight per unit than water. In terms of solubility, it mixes easily with organic solvents and resists dissolving in water—an old-school trick for extracting it from aqueous workups. The molecule leans toward reactivity because of the bromine group, which leaves the carbon framework easily in the presence of nucleophiles. The color and odor serve almost like signatures, though in labs (and especially in bulk storage), the key is controlling exposure: both volatility and reactivity mean this compound disappears fast when left uncapped or near heat.
Technical Specifications & Labeling
Every drum or flask you order comes with a set of strict details: purity percentage, commonly above 98%; the trace content of water, often less than 0.2%; and information about common stabilizers, if any are used to prevent decomposition. Regulatory frameworks such as GHS require hazard pictograms, signal words, and warnings about its flammable and harmful nature. Batch numbers track material all the way to its source. Even container type matters—amber glass limits light-triggered degradation, and vapor-tight caps keep both the user and product safe. Handling instructions appear right next to shipping documents; every label lists not just hazards but fire-fighting measures, spill protocol, and medical guidance on skin or inhalation exposure.
Preparation Method
The textbook approach begins with isopropanol or propan-2-ol as the alcohol. The alcohol reacts with a concentrated source of hydrogen bromide. In smaller lab setups, chemists often bubble dry HBr through a chilled flask containing isopropanol under reflux. As HBr protonates the alcohol, water leaves, and bromide steps in where the hydroxyl group sat, giving freshly minted 2-bromopropane. For higher yields and purity, some prefer phosphorus tribromide (PBr3), bringing more consistent conversions for big-batch synthesis. Between the methods, the choice sometimes boils down to what kind of waste by-products you can tolerate, or how much cost and time the process should demand. Technical refinements over the decades focus on keeping side-products—like isopropyl ether or propene—down to a minimum.
Chemical Reactions & Modifications
2-Bromopropane pulls its weight as both a target and a tool in synthesis. In undergraduate labs, students often use it to demonstrate the difference between SN1 and SN2 reactions—depending on the nucleophile and solvent, the reaction path slides between these regimes. The bromine atom leaves with relative ease, allowing alkylation of nitrogen, sulfur, oxygen or phosphorus nucleophiles. In industry, this property translates to using 2-bromopropane for making branched alkyl derivatives, including pharmaceuticals, fragrances, and quaternary ammonium salts. Basic hydrolysis restores isopropanol; treating it with strong bases can even drive elimination, producing propene—a simple demonstration of underlying reaction principles as well as practical synthesis.
Synonyms & Product Names
Some suppliers list 2-Bromopropane as isopropyl bromide. You may spot “1-methylethyl bromide” and “sec-propyl bromide” as alternatives, depending on the naming tradition favored by chemists or local markets. International patents and regulatory lists may flip between these descriptors, but every laboratory recognizes the CAS number 75-26-3 for official clarity. Product names change from one catalog to another, yet the underlying molecule stays fixed. If you browse reagent suppliers, expect the major players—Sigma-Aldrich, Alfa Aesar, TCI—to assign their own product codes, but the bottle contents remain consistent across the board.
Safety & Operational Standards
Anyone who’s spent time working with 2-bromopropane knows the importance of fresh gloves and a snug fume hood. The compound evaporates at room temperature and the vapors hit fast—causing dizziness, throat irritation, or worse if you outrun ventilation. Both skin and respiratory contact present real hazards. Workplaces must log every transfer, spill, or disposal, treating 2-bromopropane as hazardous waste. Fire isn't far away with a liquid that catches at 20°C. Extinguishing options rely on carbon dioxide, dry powders, or expanded foam. All the while, storing it with strong oxidizers or open flames quickly invites trouble. I remember the sharp tang of a minor fume leak in a student lab: supervisors cleared the area because overexposure, even for a few minutes, can leave you dizzy or lightheaded for an hour. Standardized PPE—goggles, nitrile gloves, flame-retardant coats—make a difference, and compliance with OSHA guidelines along with EU REACH rules forms the backbone of responsible handling.
Application Area
2-Bromopropane’s calling card shows up in specialty synthesis. One story I keep coming back to involves a pharmaceutical scale-up where a quaternary ammonium catalyst needed precise branching—something 2-bromopropane handles with less fuss and more predictable yields than chlorinated relatives. Its role as an alkylating agent extends to dyes, flavors, and various organic intermediates. In the classroom, it’s a favorite for teaching substitution and elimination reactions, giving both clarity and predictability to lab results. Its lower cost compared to more complex halides makes it a go-to resource for developing new reaction methodologies or exploring biocatalytic transformations. In the world of fine chemicals, efficiency often trumps tradition, and those who use 2-bromopropane usually cite yield and selectivity as reasons they return to it year after year.
Research & Development
Research on 2-bromopropane highlights not just its use but the deeper push to cut risks. Many projects focus on green chemistry routes, converting renewable alcohols straight to alkyl bromides under milder conditions. Some academic labs have experimented with ionic liquids or catalyzed, solvent-free syntheses, aiming to remove persistent legacy waste from phosphorus by-products. Analytical work drills down into reaction mechanisms, mapping out intermediate species with NMR and mass spectrometry. Those in surface chemistry keep exploring how brominated hydrocarbons interact with catalysts in nanotechnology and materials design. At the same time, researchers looking into occupational safety conduct air-monitoring studies and demonstrate practical ventilation improvements for minimizing exposure.
Toxicity Research
By the late 1990s, reports from South Korea raised red flags about 2-bromopropane’s health impact. Factory workers faced symptoms ranging from nausea to more chronic reproductive issues—a sobering illustration of real-world risks. Toxicologists later confirmed the substance could harm bone marrow and affect both male and female reproductive organs with sufficient exposure. Animal studies showed dose-dependent toxicity: short-term exposure caused central nervous system depression, and long-term chronic doses led to much more serious problems. As a result, health agencies established tighter workplace exposure limits and called for improved air monitoring. Chemists must respect these boundaries: awareness of 2-bromopropane’s risks should shape every decision from container selection to waste disposal.
Future Prospects
The story of 2-bromopropane isn’t set in stone. Market shifts already push chemists toward greener alternatives, yet no universal replacement matches its performance in all applications. Ongoing studies examine brominated solvents that degrade more rapidly or show less persistence in the environment, while sustainable feedstocks promise to reduce the carbon footprint of halide production. Digital documentation and full-life-cycle analysis cover each batch, driven by regulatory trends and the rising cost of incident management. The hope is that new synthetic routes for 2-bromopropane will rely less on hazardous precursors and that every safety lesson learned finds direct application in lab design and industrial protocols. Continued vigilance and innovation keep this compound useful but safe—a balance every researcher, production manager, and health officer strives to maintain as chemistry moves forward.
2-Bromopropane: Beyond the Letters and Numbers
People in labs and classrooms see a name like “2-Bromopropane” and expect just a formula, but knowing what those formulas mean has real-world value. The formula for 2-Bromopropane comes out as C3H7Br. Underneath those five characters sits a blueprint for how this molecule shapes its own role in science and industry. Some folks might shrug, thinking it’s just another abstraction, but in practice it guides everything from daily safety routines in chem labs to big-picture health policies and industrial synthesis on factory floors. I’ve watched researchers hesitate over bottles with similar names, double-checking labels and paperwork. All those habits stem from the nitty-gritty details in these formulas.
The Make-Up: What That Formula Tells Us
Chemical formulas act almost like a signature, showing you exactly what goes into a molecule. With 2-Bromopropane, three carbon atoms joined up with seven hydrogens and a single bromine. This stuff fits under the category of haloalkanes—hydrocarbons with a halogen attached. The “2-” marks where the bromine lands on the propane’s backbone; spot two, not the end. That slight change can swing the molecule’s physical and chemical behavior. A student once told me he didn’t see why it mattered much—a carbon is a carbon, right? But swap the bromine’s position and the way this compound interacts with your body, your environment, and your lab equipment can shift.
Real-World Risks and Practical Experience
Plenty of people outside chemistry circles rarely cross paths with 2-Bromopropane. In workplaces, though, it's a different story. This chemical gets used as a solvent and in certain industrial syntheses. That chemical formula means more than numbers—it tells safety officers how to handle spills and plan emergency response. People working with brominated organics already know the distinct sharp odor, the irritation it can bring, the need for good ventilation. Regulations didn’t just drop from a rulebook out of nowhere; they came from incidents where ignoring raw chemistry put workers at risk. News spread fast after reports of neurological illness among workers exposed to it in adhesive production, pushing changes in how industries protect their staff.
The Importance of Clarity and Shared Knowledge
One thing folks tend to skip over with chemical names is just how close some look and sound. Small changes in formulas mean big differences in hazard level, application, and how you dispose of waste. In teaching, I’ve caught students mixing up 2-Bromopropane with its cousin, 1-Bromopropane, just because the bottle labels look similar and the formulas differ by a single digit. That single switch mattered so much, with some local labs overhauling their inventories after realizing the simple error could lead to improper storage and unsafe conditions. Chemical formulas deserve care, attention, and wide sharing because everyone down the line relies on them—from the chemist wearing gloves to the environmental inspector checking groundwater for contamination.
Supporting Safer and Smarter Work
Clarity in chemical formulas like C3H7Br gives people things they can count on: right safety protocols, targeted research, and wiser policy. Trouble always seems to start with a shortcut—someone treating one similar-sounding substance like its safer twin. Better education using these basics, regular refresher sessions, and a culture of double-checking in the lab or plant floor go a lot further than one-time warnings or printouts taped to the wall. Facts like this—simple, reliable, and scientifically verified—fuel better conversations, smarter uses, and stronger health for people and the places they work.
Everyday Chemistry and Real-World Impact
2-Bromopropane may not be a household name, but it runs behind the scenes in labs and factories across the globe. Tucked into glass bottles or steel drums, this compound shapes several industries—often quietly, sometimes with more controversy than you’d guess from a simple clear liquid.
Punching Above Its Weight in Organic Synthesis
Talk to anyone working with organic chemistry, and you’ll hear about alkyl halides like 2-Bromopropane. It quickly gives up its bromine atom, making it a handy tool for introducing isopropyl groups onto carbon chains. In practice, chemists reach for it when they want to make something stick—building blocks for pharmaceuticals, new dyes for textiles, and specialty solvents. Its ability to act as an alkylating agent brings variety to lab benches and mass production lines. Some familiar examples: intermediates for painkillers or antihistamines, and colorants that give certain plastics their look.
A Quiet Role in Solvent and Cleaning Mixtures
Researchers and factories depend on solvents with just the right performance. 2-Bromopropane makes its way into solvent blends, sometimes excelling as a degreaser or paint remover. Its presence boosts cleaning power where oil and sticky residues need to disappear—electronic parts, metal car components, or optical filters. Anyone who’s spent hours scrubbing caked-on grease appreciates the difference. It often steps in where chlorofluorocarbons are now frowned upon due to environmental rules. Still, safety has become a rising concern, pushing companies to keep a sharp eye on exposure and alternatives.
Pharmaceuticals and Agrochemicals: Small Piece, Big Picture
Drug makers rarely shout about their raw materials, but 2-Bromopropane shows up as a cornerstone for molecules that eventually become part of pills and treatments. Its ability to help stitch together carbon bonds has driven new generations of active ingredients. Agrochemical labs rely on it, too, to shape herbicides and insecticides. Trace it through a supply chain, and you’ll land at fields that produce more food with fewer pests—silent, essential background work for global agriculture.
Looking Closely at Safety and Sustainability
Not all uses come without controversy. Chronic exposure brings risks. Workers have suffered nerve damage in poorly ventilated spaces, leading regulators to clamp down on proper use and limit workplace contact. Responsible facilities take air monitoring seriously and train teams on safe handling. Plenty of room for improvement remains in some regions, especially where oversight lags behind scientific evidence. Awareness, flexible ventilation, and protective gear lower the risk. Some manufacturers have already started moving toward greener alternatives, especially in fields like electronics, where customer demand and regulations push hard for safer cleanup chemicals.
Chasing Less Harmful Alternatives
Switching to new solvents takes effort and cash, but rewards stretch far. Research teams experiment with less hazardous compounds that can fill the same roles as 2-Bromopropane. Shareholders, regulators, and employees call for a shift—not just for better worker health but for a clearer environmental conscience. Industry groups, scientific teams, and non-profits play a part, spreading success stories and pushing for change where it’s slow to come. Sometimes, the push for safety starts with a single factory or a dedicated health advocate and then spreads much further.
Knowing the Substance: Why Care Matters
Walk into any chemical storeroom, and you'll notice that every bottle has a story. Some stories come with more caution tape than others. 2-Bromopropane fits into the “watch out” category for good reason. It’s a clear liquid that might give off an ether-like smell, but the real concern lies behind those invisible traces. Breathing in vapors or letting it touch the skin can lead to nasty health effects. So, thinking about safety with this chemical isn’t paranoia; it’s pretty much just self-respect.
The Risks Aren’t Hype—they’re Well-Documented
People handling 2-Bromopropane have reported everything from headaches to much bigger trouble like nervous system issues, bone marrow suppression, fertility problems, and even cancer risk, as the International Agency for Research on Cancer (IARC) references. It’s not just those working in high-volume production—anyone handling even modest amounts gets exposed if care slips. Chronic exposure can sneak up, and that’s not the kind of surprise anyone wants.
Sensible Gear: No Cutting Corners
Lab coats and goggles aren’t fashion statements. They really do keep burns and splashes off your body. The gloves matter, too. Nitrile or neoprene will actually stop breakthrough; not every glove does the trick. Wraparound eye shields stop stray splashes and keep hands away from the face. Good ventilation makes the difference between a safe space and a slow leak into your lungs. Fume hoods pull away vapors, so you’re not standing there breathing in a chemical cloud.
Storage with a Systems Mindset
Chemicals never take a day off. Leave a bottle in the wrong spot, and it’ll let you know. For 2-Bromopropane, keeping it tightly sealed and out of sunlight saves everyone trouble. This liquid plays badly with oxidizers and strong bases, so stack it away from these old rivals. Temperatures should sit cool and steady. Label everything clearly—the last thing anyone wants is a mixing mistake during a busy shift.
Spills: Act Fast, But Don’t Wing It
Even careful hands can knock over a flask at some point. Speed counts, but so does sticking to what’s proven. Clear the area, especially if there’s no fume hood around. Suit up in protective gear before dealing with a puddle. Absorbent pads are handy for the small stuff. Shovel and seal any contaminated material in the right disposal drum. Rinse the spot with water, but only if local safety rules say it’s okay.
Waste Lives on after the Lab
Pouring leftover 2-Bromopropane down the drain is short-sighted and pollutes for the long haul. Chemical waste streams need labeling and containment—no gray areas. Follow local rules, hand it off to certified disposal folks, and keep records clear. If you’re guessing, odds are someone down the line pays for that mistake in groundwater or air quality.
Training and Habits: The Everyday Shield
No technical skill beats simple awareness. Regular safety training helps habits stick and closes knowledge gaps before mistakes grow wings. Knowledge isn’t static; refreshers and honest talk from experienced coworkers make sure nobody gets caught off guard.
Building a Culture Where Safety Isn’t an Afterthought
Places that put safety up front see fewer accidents and more trust. Shortcuts with 2-Bromopropane have too high a price—for health, for the environment, for reputation. Respect for the chemical means respect for everyone who comes in contact with it.
Looking at the Real Risks of 2-Bromopropane
2-Bromopropane sometimes pops up in chemical plants and research settings, often as a solvent or an intermediate for making other chemicals. Anyone who’s ever spent time in a lab or worked in manufacturing has probably come across a notice about chemical safety. My own work in a research lab made me familiar with stacks of chemical data sheets. We’d always check the shelf for the telltale orange and black hazard label—2-Bromopropane is no different.
People want to know if this chemical is something to worry about. That makes sense: a few years back, cases from South Korea showed that workers got sick after handling 2-Bromopropane without enough protection. It wasn’t a minor issue. Reports from the late 1990s showed that factory workers exposed to high concentrations suffered nerve damage, reproductive problems, and effects on their blood. These aren’t small side effects. For instance, women exposed long-term sometimes lost their periods. Men showed lowered sperm count. In my experience reviewing chemical safety files, I found that those outcomes quickly got flagged as red-alert health problems.
Understanding How it Affects the Body
The science says that 2-Bromopropane enters the body mostly by breathing it in or absorbing it through the skin. Eyes and skin get irritated during direct contact, which sounds common for a lot of chemicals, but there’s more going on beneath the surface. Breathing in too much of it can mess with nerve cells. According to reviews from organizations like the National Institute for Occupational Safety and Health (NIOSH) and the World Health Organization (WHO), the chemical can impact not just nerves and fertility but also the blood’s ability to make new, healthy cells.
Labs and factories often screen for these health effects in their workers. I remember doctors running nerve tests for anyone exposed to certain solvents, and the rules around 2-Bromopropane reflect that same need for caution. The Centers for Disease Control and Prevention (CDC) and the European Chemicals Agency (ECHA) both say that anyone who spends time working with this compound should keep skin covered and use fume hoods. Employers must stick to safety rules, setting exposure limits in the air. That can be a challenge, especially if machines aren’t ventilated well or workers skip protective gear because it’s hot in the plant.
Preventing Harm Inside and Outside the Lab
In the lab or factory, safety starts before opening a bottle. Training matters. I’ve seen places cut corners on simple things like gloves or goggles, thinking it’ll save money. Those shortcuts come at a real cost if someone gets sick. Updated safety sheets, regular health checks, and easy access to proper gear change the story. Factories using better airflow, personal air monitors, and regular reviews rarely see major incidents.
On a bigger scale, industries can look at alternatives. Some countries banned or tightly restricted 2-Bromopropane after health scares. That can push companies to use less hazardous chemicals—safer for people and often for the environment too. Green chemistry isn’t just a buzzword here; it means fewer workers take those long-term health hits.
More research keeps coming out about the risks. When new evidence shows harm, regulations need to keep up. Transparency helps as well: employers must talk honestly about risks, and health agencies should keep sharing updates from current studies. That saves lives, plain and simple.
Let’s Face It—Chemicals Need Respect
Some folks think a bottle of 2-bromopropane fits just fine on any old shelf. I’ve seen it in university labs, the jug stuck behind dusty solvents someone forgot about after graduation, labels half-peeled. This attitude gets people hurt. 2-Bromopropane doesn’t shout danger with flashing lights, but that doesn’t mean ignoring it is wise. This stuff is flammable and can give off harmful vapors. Inhalation risks, skin contact problems, and the fact that it's a halogenated compound mean you want solid routines in place. Safe storage isn’t about following checklists for the sake of looking professional; it’s about people making it home in one piece.
Think Temperature, Think Light
2-Bromopropane isn’t the most volatile chemical, but it won’t thank you for sunlight or erratic heat. I learned this the hard way after finding a container sweating oil because someone left it in direct sun. Cooler, stable temperatures work best—below 30°C is a good target. Store it away from radiators, windowsills, or places that heat up unpredictably. Sunlight not only bumps up the temperature but can trigger reactions you’d rather avoid. Bulky chemical storage cabinets with sturdy doors and ventilation offer the peace of mind you can’t buy from prayers.
Seal That Lid, Watch That Label
Sometimes I find cans missing their screw-tops, a funnel stuck in the neck for quick pours. Convenience isn’t worth the risk. Keep containers shut tight, with original caps or chemical-resistant lids. Vapors aren’t just an annoyance; repeated exposure to 2-bromopropane can trigger headaches or worse. Fuzzy labels cause mix-ups. Permanent marker fades. Laminated, printed labels with hazard symbols last longer and stop accidents before someone grabs the wrong jar.
Keep It Far From Flames and Sparks
No matter how safe a workspace looks, electronics, heating plates, and even faulty wiring can kick up an unexpected spark. Flammable vapors don’t care about intentions—give them a chance and they’ll ignite. Storage must separate 2-bromopropane from open flames, sparks, and anything that can light up a vapor trail. Chemical storage guidelines recommend a dedicated, spark-free chemical storage cabinet with tight doors and little chance of static buildup. Spark prevention takes little effort and saves a world of headaches.
Think About Who Else Shares the Space
Leaving chemicals within reach of untrained hands is asking for trouble. My old community lab had a strict logbook for every bottle: who took it, what they did, and which bench it visited. Even if working solo, keep a log or at least let others know what’s stored and where. Surprises cause delays in emergencies. If another chemical leaks or spills nearby—say, an oxidizer or strong acid—mixing with 2-bromopropane can make bad situations worse. Segregation in storage pays off.
Ventilation Isn’t Optional
Too many times I’ve watched someone wedge chemicals in a musty closet to “keep them out of sight.” Poor airflow lets vapors pool up. 2-Bromopropane won’t give a forgiving cough if people spend too long in a space without ventilation. Use cabinets with ducted ventilation systems or at least ones set up with vent holes near the top and bottom. A room where the air feels stale risks everyone’s health, not just your own.
Wrap-Up: Attitude Makes All the Difference
Storing 2-bromopropane safely comes down to habits. Lock it up, label it right, separate it from dangers, and let everyone know what’s there. Good storage habits didn’t just come from one mistake—they came from watching what goes wrong when people get careless. That’s not something you want to experience yourself.
| Names | |
| Preferred IUPAC name | 2-Bromopropane |
| Other names |
Isopropyl bromide
2-Propyl bromide 1-Methylethyl bromide |
| Pronunciation | /tuː ˌbroʊməˈproʊpeɪn/ |
| Identifiers | |
| CAS Number | 75-26-3 |
| Beilstein Reference | 1718734 |
| ChEBI | CHEBI:63813 |
| ChEMBL | CHEMBL301765 |
| ChemSpider | 7336 |
| DrugBank | DB14085 |
| ECHA InfoCard | 14af4d23-20a9-476b-8f3e-221ac9aad25e |
| EC Number | 200-864-0 |
| Gmelin Reference | 8085 |
| KEGG | C01734 |
| MeSH | D017225 |
| PubChem CID | 6576 |
| RTECS number | TX9625000 |
| UNII | R3P60KDM7A |
| UN number | UN2344 |
| Properties | |
| Chemical formula | C3H7Br |
| Molar mass | 122.99 g/mol |
| Appearance | Colorless liquid |
| Odor | Sweet odor |
| Density | 1.31 g/mL at 25 °C (lit.) |
| Solubility in water | Slightly soluble |
| log P | 1.764 |
| Vapor pressure | 3.58 kPa (at 20 °C) |
| Acidity (pKa) | 40 |
| Magnetic susceptibility (χ) | -62.4×10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.435 |
| Viscosity | 0.46 mPa·s (20 °C) |
| Dipole moment | 2.05 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | (276.6 J·mol⁻¹·K⁻¹) |
| Std enthalpy of formation (ΔfH⦵298) | -34.7 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -1997 kJ·mol⁻¹ |
| Hazards | |
| GHS labelling | GHS02, GHS07 |
| Pictograms | GHS02, GHS07 |
| Signal word | Warning |
| Hazard statements | H225, H319, H336 |
| Precautionary statements | P210, P280, P305+P351+P338, P337+P313 |
| NFPA 704 (fire diamond) | 1-2-0 |
| Flash point | 10 °C |
| Autoignition temperature | 410 °C |
| Explosive limits | 1.8–8.8% |
| Lethal dose or concentration | LD50 Oral Rat 1,870 mg/kg |
| LD50 (median dose) | LD50 (median dose): Oral-rat LD50: 2800 mg/kg |
| NIOSH | RA1585000 |
| REL (Recommended) | Keep container tightly closed in a dry and well-ventilated place. |
| IDLH (Immediate danger) | 800 ppm |
| Related compounds | |
| Related compounds |
Bromomethane
1-Bromopropane 2-Chloropropane Isopropanol Propane |
