1-Bromo-2-Chloroethane: An Expansive Look at Uses, Risks, and Research
Historical Development of 1-Bromo-2-Chloroethane
In the late nineteenth century, halogenated ethanes began catching the attention of laboratory pioneers. 1-Bromo-2-chloroethane emerged from a growing understanding of how subtle tweaks to hydrocarbons could bring dramatic shifts in reactivity. By adjusting the combination of bromine and chlorine atoms in the molecular backbone, early chemists started seeing possibilities for specific reactions not possible with simple ethane. As laboratory glassware improved and new reagents became available, focus shifted to making these compounds reliably, paving a path that made halogenated ethanes increasingly common in organic synthesis and industrial settings. These changes echo the larger trend of chemical manufacturing: one small experimental breakthrough ripples through entire industries. My own experience working with older chemical literature highlights how even modest advances—like a more consistent route to 1-bromo-2-chloroethane—can open doors to a world of downstream products, including pharmaceuticals, agrochemicals, and specialty polymers.
Product Overview
1-Bromo-2-chloroethane sits in the toolkit of chemists who value selectivity and control over reactions, thanks to its two different halogen leaves on a short ethane stem. Its chemical signature appeals to those seeking to introduce both bromine and chlorine into organic frameworks fast. As commerce started scaling up the production of halogenated compounds, 1-bromo-2-chloroethane found a foothold in research labs and manufacturing plants. Its role ranges from an intermediate in making more complex molecules to acting as a solvent or reaction medium in specific syntheses where its blocky nature shuts out unwanted side reactions. Demand in the specialty chemicals industry, especially in pharmaceuticals and novel materials, keeps this compound relevant.
Physical & Chemical Properties
The compound brings together a dense, oily feel with a sharp, slightly sweet chemical odor. It sports a boiling point in the neighborhood of 106–110°C, meaning it won’t evaporate at room temperature but still needs careful storage to avoid losses from slow evaporation or leaks in lab containers. The liquid’s density hovers above water at roughly 1.6 g/cm³, and this heaviness shows itself quickly if you ever spill it: drops sink and disperse slowly in aqueous mixtures. Solubility remains modest in water but much higher in many organic solvents like ether or chloroform. Chemical reactivity focuses on the two halogen atoms—a bromine and a chlorine—each offering different speeds and selectivities when the molecule jumps into reactions. The carbon-bromine bond loves to break first, which lets the compound act as both an alkylating and halogen transfer agent.
Technical Specifications & Labeling
Suppliers who understand the needs of research and industry specify purity grades, water content, and halide impurities. In practice, buyers expect over 98% purity for most applications. Gravimetric and spectrometric methods back up these claims, and regulatory labeling covers hazards like skin and eye contact, inhalation risk, and flammability. Drum and bottle labeling clearly display CAS numbers, hazard pictograms, and emergency procedures—details I find essential on the bench where mistakes happen and clarity makes all the difference. Companies handling ton lots tend to track batch origins carefully, so traceability stays locked in from synthesis to final use.
Preparation Method
The main preparative route starts from ethylene dichloride or vinyl chloride, passing through a substitution sequence with hydrobromic acid or bromine. Reaction control matters; temperature, time, and proportions need tuning to avoid forming dibromoethane or dibromo derivatives, which complicate isolation. Fractional distillation or column chromatography finishes the job, delivering a clear, pungent-smelling liquid. Lab-scale chemists can whip up small batches with strict observance of ventilation and protective equipment because both precursors and the product itself pack considerable risks. In the past, cruder methods brought a lot of byproduct, but more modern routes have sharpened yields and reduced waste.
Chemical Reactions & Modifications
1-Bromo-2-chloroethane plays nicely in nucleophilic substitution reactions, especially as a precursor for molecules that need two different halogen handles for further transformation. Alkoxide anions latch onto the molecule easily, pushing the bromine out and letting chemists build up ethers, esters, or even cyclized compounds. The presence of two distinct halogens lets researchers achieve selective functionalization, handy for multi-step syntheses in medicinal chemistry. In the hands of skillful chemists, selective reduction or elimination can yield chloroethylene or even alkenes with distinct placement of leaving groups. As a participant in Grignard or lithium-halogen exchange reactions, it lends flexibility to the lab without forcing a one-size-fits-all approach.
Synonyms & Product Names
You’ll find 1-bromo-2-chloroethane on shelf labels as Ethane, 1-bromo-2-chloro-, 1-Chloro-2-bromoethane, and even Bromochloroethane. For those searching older texts, the synonyms just keep coming. CAS Number recognition (107-04-0) goes a long way to avoiding confusion, especially in global commerce where product codes can differ widely. Talking from experience, using synonyms with less experienced researchers can stir up costly mix-ups—sticking to one naming system in the lab logbook cuts those headaches out quickly.
Safety & Operational Standards
Laboratory safety protocols call for extra care with this material, since both vapor and skin exposure can cause irritation or worse. Inhalation risks include headaches and drowsiness, consistent with its volatility and density. Protective nitrile gloves, eye shields, and the best possible ventilation stay front and center. Fire safety matters, too—the compound ignites with a strong enough spark or open flame, and burns with release of corrosive hydrogen halides. Industrial facilities design their handling systems with sensors and containment, relying on spill kits and training refreshers so no one forgets what’s at stake. From my own years in teaching labs, running safety drills with chemicals like this always brings home just how quickly small lapses can snowball.
Application Area
In the real world, 1-bromo-2-chloroethane takes center stage during organic synthesis—turning up in pathways that lead to pharmaceuticals, pesticides, polymers, and specialty coatings. Medicinal chemists use it for introducing halogenated motifs that tweak metabolic behavior or boost molecular stability. Research settings lean on it to build up uncommon structures in probe molecules, while industrial plants see it as a step on the route to fire retardants or plasticizers. Its ability to offer selective alkylation supports those looking for functional group control. That balance of reactivity, selectivity, and manageability keeps it relevant despite competition from newer or less hazardous alternatives.
Research & Development
R&D teams still find new tricks for this molecule, exploring its role in alternative alkylating agents, or testing it against newer, greener solvents. In my own collaborations, we chased analogs for better pharmacokinetics, using its backbone to investigate how different placements of bromine and chlorine affect biological activity. Academic work in reaction mechanism continues to use it as a predictable test case for studying nucleophilic substitutions, elimination dynamics, or chain transfer in polymerization. Analytical chemists fine-tune detection methods in soil and water, keeping pace with new regulations. These efforts collectively drive re-assessment of how the chemical can fit in safer, more sustainable workflows.
Toxicity Research
Toxicologists give 1-bromo-2-chloroethane close scrutiny due to its volatility and halogen content. Inhalation studies and laboratory animal research warn of central nervous system effects, respiratory irritation, and some degree of hepatotoxicity. Skin contact, even brief, causes burns in enough cases for lab safety committees to require gloves every time. Chronic exposure risks include liver and kidney effects, so workplaces install strict monitoring protocols. Environmental fate studies show moderate persistence with the risk of groundwater leaching, raising calls for improved disposal and spill response methods. Discussions with industrial hygienists drive home how rapid communication and awareness can stop small exposures from stacking up into bigger problems across entire teams.
Future Prospects
The landscape for 1-bromo-2-chloroethane will only get rockier as regulators challenge halogenated organics with tighter limits on emissions and exposure. At the same time, the need for finely tuned intermediates in drug manufacture won’t let the molecule vanish overnight. Technology advances in containment, waste treatment, and reaction design can soften the environmental impact. Researchers worldwide test alternative reagents or solvents that mimic the chemical’s utility but dial down its hazards. Having seen progress in green chemistry over two decades, I expect to see this compound eclipsed eventually, but not before new generations squeeze every possible use out of it, weighed against costs to health and ecosystem. Success here relies on combining deep technical know-how with respect for evolving safety and environmental standards.
The Role in Organic Synthesis
1-Bromo-2-chloroethane rarely gets talked about outside of specialty labs, but it plays a quiet yet strong role in organic chemistry. Its real strength shows up as an intermediate. Chemists often rely on it for introducing both bromine and chlorine atoms into carbon frameworks, which brings flexibility to synthetic pathways that others can’t match. The halogen atoms have different reactivity, giving researchers creative freedom when building up complex molecules. For folks working on new pharmaceuticals or specialty chemicals, having a compound that can behave as both a source of bromine and chlorine lets them try out multiple approaches without loading their bench with extra chemicals.
Applications in Pharmaceuticals and Research
I’ve seen graduate students pull out 1-bromo-2-chloroethane during late-night sessions while chasing a tricky alkylation or exchange reaction. Drug discovery often demands non-standard starting points, and this compound answers that call, introducing dual functionalities in a single step. New molecules in cancer or antiviral research benefit from the synthetic shortcuts this compound offers, which can turn long, multi-step procedures into more manageable projects. Scientists at big pharmaceutical companies and academic labs keep it on their chemical shelf for these reasons alone. Its value jumps further in radiolabeling work, especially when paired with isotopes for imaging or metabolism studies, providing a backbone for careful tracking and measurement inside living systems.
The Place in Material Science
People often overlook niche chemicals in the rush to talk about “breakthrough” materials, but some advances in plastics or specialty polymers come straight from humble building blocks like 1-bromo-2-chloroethane. Polymer chemists use this compound to make custom monomers. The halogen pair opens routes to add different side groups onto carbon chains—building plastics with specific mechanical or thermal properties. I remember a small startup in the coatings sector that improved their product’s weather resistance by using a derivative they’d traced back to this exact compound. Its role isn’t flashy, but it feeds into applications with real-world value, from electronics insulation to improved adhesives.
Synthetic Pathways in Agricultural Chemicals
Crop protection often starts with a molecule that lays the groundwork for selective toxicity. 1-Bromo-2-chloroethane has found a niche in the synthesis of key intermediates for herbicides and pesticides. Getting precise halogenation patterns gives these chemical agents their biological effect, and this compound provides that tool. Manufacturers depend on reproducible, scalable reactions—using starting points that are both reactive and predictable. Chemists who work in agrochemical R&D rely on such intermediates, knowing small changes introduced early can give major improvements later, like reduced toxicity to non-target plants and wildlife.
Safety and Handling Considerations
I’ve never handled this material without pausing for a safety check. 1-Bromo-2-chloroethane brings the hazards you’d expect from a haloalkane. It can irritate skin and lungs, and the environmental impact isn’t minor if accidental release occurs—halogenated organics tend to stick around and cause trouble in soil and water. Proper lab ventilation, gloves, and waste collection systems stay non-negotiable. More sustainable methods and safer alternatives belong on the industry’s radar, especially as regulations tighten and environmental scrutiny grows. Training young chemists in safe, respectful handling stays just as important as teaching them reaction mechanisms.
Understanding the Risks
1-Bromo-2-chloroethane serves a purpose in organic chemistry labs and industrial work. Despite its usefulness, the stuff carries some real dangers. It gives off fumes with a biting, sweet-ish smell that can sting your nose if you aren’t careful. You won’t always see it coming, either—this chemical can irritate or even burn the skin, eyes, and lungs. Years ago, in my own lab, I watched a colleague struggle with a painful eye burn after a splash bounced out of a poorly capped vial. That image still pops into my mind every time I roll out the chemical hood and snap on my goggles.
Personal Protection Makes All the Difference
A tiny oversight can mean a trip to the clinic. Splash goggles matter—a regular pair of glasses won’t cut it for this compound. Gloves stand between you and trouble, but not every glove blocks these halogenated compounds. I always reach for nitrile rather than latex, since latex gloves sometimes let solvents slip right through. Lab coats aren’t just a uniform. After a few ruined shirts, I learned it’s easy for droplets to roll off a sleeve and straight onto your skin. Closed shoes wrap it all up, shielding your feet from the worst-case scenario.
Tips for Handling and Storage
I’ve seen people pour volatile solvents straight onto the open bench. A hood protects you from fumes that can inflame your throat and lungs. There’s no sense in risking it. Storage matters, too. I always keep those bottles in well-ventilated, labeled cabinets, away from acids and bases. Taking the cap off for even a minute in open air can flood a small lab with vapor. Learn to work quickly, cap bottles immediately after each use, and check glassware for cracks that might cause leaks or spills under pressure.
Spill and Emergency Know-How
If a spill happens, time turns into the enemy. I used to freeze up in the early days, but now I’ve learned to act fast. Baking soda and cat litter work for some old-school spills, but with 1-bromo-2-chloroethane, I use a lab-ready absorbent pad, then move all other chemicals out of the way. I grab the spill kit before I even uncork the bottle, so I’m not scrambling for it while dangerous liquid sits on the bench. Clean the spot, double-bag the waste, and don’t forget that any splash on clothes means a shower and a change—no exceptions. Wash the area again with soap and water, even after it looks clean.
Why Ventilation Matters
A jammed hood or a broken fan invites trouble. Regular maintenance keeps the risk of fumes low. An old filter or a blocked duct can lead to chemical exposure without warning. Keep a log of when maintenance happens. If a room suddenly smells strange or the airflow feels weak, call in a technician before another beaker even comes out. Sometimes, you only get one warning before serious harm happens.
Looking Ahead with Safety Culture
Continuous reminders, like safety meetings and visible signage, help keep mistakes from becoming tragedies. Sharing stories, especially close calls or lessons learned, makes protocols feel personal. Building a culture that pins safety above speed means no shortcut ever wins out over health. The person in the next chair counts on you to follow through—just as you expect from them.
Chemical Formula: C2H4BrCl
Walking into any chemistry lab, 1-Bromo-2-Chloroethane might just smell like another chemical bottle on the shelf. Its chemical formula, C2H4BrCl, describes a two-carbon chain where a bromine and a chlorine atom each take the place of a hydrogen on neighboring carbons. The simplicity of that structure means you won’t confuse it with more complicated organics, but its straightforward makeup also makes it useful in synthetic pathways requiring reliable, predictable reactivity.
Molecular Weight: 143.41 g/mol
Chemists don’t always get excited about a number like 143.41, but the molecular weight of 1-Bromo-2-Chloroethane sits right in a sweet spot. It’s heavy enough for phase separations to be clear and for mass spectrometry to pick out without background clutter. Weighing out compounds in undergraduate labs, I always noticed how the bromine and chlorine atoms add noticeable heft, offering tangible proof that tiny atomic differences can affect a liquid’s presence in your hand. This weight also nudges the boiling point higher than simple chloroethane or bromoethane, which sometimes makes it easier to handle without racing vapors in a warm lab.
Behind the Numbers: Why Formula and Weight Matter
Ask most researchers what matters, and they’ll point to the formula and weight immediately. You need to calculate molar amounts precisely, especially for reactions that hinge on stoichiometry. Get it wrong, and yields plummet or worse, the experiment goes sideways altogether. The difference between C2H4BrCl and a close cousin with, say, two chlorine atoms changes more than just a label—chemical reactivity wiggles in unexpected directions. That unpredictability is why even seasoned chemists triple-check reagent purity, especially for halogenated organics.
Having access to reliable data isn’t just a matter of curiosity. 1-Bromo-2-Chloroethane falls under tightly regulated categories in plenty of countries due to hazardous nature. Improper labeling can lead to accidents or, worse, regulatory headaches. Looking back in my own graduate research days, I remember a mix-up between bromo compounds left a neighbor’s distillation column clogged with tar and more than a hint of exasperation all around; simple as it sounds, knowing the exact formula and weight prevents crises of both safety and productivity.
Broader Impact: Handling and Use
Chemical literacy goes a long way. Safety Data Sheets ask for accuracy at every step. Spill response protocols, proper disposal, and even emergency procedures connect directly to the molecular weight—chemists need this information to estimate volatility, toxicity, and reactivity with water or other lab agents. Missing this fundamental knowledge can turn a routine experiment into a dangerous one.
Reliable supply chains depend on correct labeling. Researchers expect bottles to contain exactly what they say, while regulators hold distributors accountable for accuracy. Errors in basics like the chemical formula or molecular weight can have cascading effects, from botched analytical experiments to contaminated products.
Clear information empowers better decisions, safer workspaces, and higher trust between manufacturers, buyers, and the scientists relying on these chemicals. In a world where one atom can spell the difference between a life-saving medicine and a hazardous byproduct, there’s no room for guesswork. 1-Bromo-2-Chloroethane shows how the basic fundamentals in chemistry set the stage for real action in the lab and beyond.
Getting Serious About Chemical Safety
Working with 1-Bromo-2-Chloroethane calls for more than just following a set of instructions. It demands respect for the risks tied to this compound. The sweet, pungent smell says a lot about its volatile nature, and anyone who has spent time in the lab knows that this isn’t something you leave lying around. I recall the first time I encountered this clear, colorless liquid—an old mentor leaned in and offered a tried-and-true rule: treat every volatile organic with care, lock it down, and keep it out of the sun.
Let's Talk Real Storage
Step into most well-run chemical storerooms and you won’t find flammable chemicals mixed in with acids or oxidizers. 1-Bromo-2-Chloroethane sits firmly in the halogenated hydrocarbon family, demanding separation from bases, oxidizers, and any reactive metals. Even a minor spill with the wrong neighbor invites chaos. It just makes sense to keep it on a shelf designed for organohalides, preferably in a cool, air-conditioned space away from all sources of ignition.
Some folks toss around the words “cool and dry.” In practice, this means not storing bottles next to a sunny window or heat source. From my time in research, refrigerators built for chemicals—not the break room kind—deliver the dependability you need for compounds with a strong vapor signature. Ventilated storage lessens the risk of fumes hanging around, which matters if a cap is not sealed tightly. Regular inventory checks and clear labeling make life easier for everyone, from the new guy on shift to the seasoned chemist scrambling for something in the back row.
Facts That Make a Difference
Flash points and vapor pressure charts aren’t decorations—they change how people treat chemicals like 1-Bromo-2-Chloroethane. Its flash point hovers under room temperature, which means even a mild summer afternoon presents real danger. According to the National Institute for Occupational Safety and Health (NIOSH), chronic exposure may lead to health issues ranging from skin irritation to nervous system damage. Each label stands as a reminder: gloves, goggles, and fume hoods aren’t optional. One splash on bare skin, and remorse arrives fast.
Why Policy and Training Matter
It’s tempting to treat storage as an afterthought, but a single misstep can set off alarms, evacuations, or even injuries. Seriously, I’ve seen a cracked cap escalate into a full-on incident. Proper secondary containment, like using trays or bins, catches leaks and keeps accidents minor. Things like chemical spill kits and immediate access to Material Safety Data Sheets (MSDS) build a culture of preparedness. Smart policy stands on the shoulders of these real-world details—the routines that build muscle memory and stop mistakes before they start.
Better Habits, Fewer Errors
Taking shortcuts trips up even experienced teams. Sharing stories about mishaps creates teaching moments that laser-focus everyone’s attention—nothing compares to hearing how a stale, rarely-inspected container warped in storage and almost emptied its contents across the floor. Regular reminders beat complacency; learning from industry bulletins or community alerts reinforces the core message: every bottle is a potent risk if handled carelessly. By blending habit, respect, and open communication, the gap between safety theory and daily practice narrows.
Simple Steps Build Consistent Safety
1-Bromo-2-Chloroethane demands focus. Keeping it secure, tracking its location, sharing safety lessons, and always gearing up with the right equipment—all these habits matter. Labs stay functional and disasters remain only stories when people treat storage not as an afterthought, but as a daily discipline rooted in respect for the chemicals in their care.
1-Bromo-2-Chloroethane: A Closer Look at Its Physical Qualities
1-Bromo-2-chloroethane does not attract the same attention as everyday substances like table salt or gasoline. Even so, it has a collection of physical properties that mean something in both research labs and chemical manufacturing. Stretching my own experience from time spent around chemical stockrooms and bench-scale synthesis, subtle quirks of certain compounds often make or break an experiment. 1-Bromo-2-chloroethane shows clear-cut signals of its own nature from the bottle to the balance scale.
Appearance and Smell Speak Volumes
Most technicians spot it right away: this liquid comes colorless and gives off a pungent, ether-like odor. This smell lingers in the air, warning you to crack a window and get some ventilation. Once, a poorly capped vial made half the lab hustle around in search of the source. It gets into the nose fast — a reminder that safe handling tops the list, even before you pop the cap.
How Heavy, How Runny?
Density tells a lot about a substance. This liquid sits at around 1.60 grams per cubic centimeter — a good chunk heavier than water. Splash some out and it pools right up, pushing water aside. That weight can play tricks on your glassware, especially when pipetting. More than once I’ve seen students expect it to layer on top, only to find it sitting stubbornly beneath.
The viscosity doesn’t stray much from that of simple organic liquids, either. It pours without real resistance, making measurement straightforward if you’re keeping an eye on the scale. As for solubility, water rejects it outright. Drop it in, watch the two separate into layers. Yet, blend it with organic solvents — ether, chloroform, acetone — and you get a clear solution, which makes it an option for some liquid-liquid extractions or syntheses that steer clear of aqueous systems.
Where Heat Begins and Ends
Boiling at roughly 108–110°C, this compound needs careful attention on a hot plate. Step away and the room could fill with vapors, since its volatility surprises unsuspecting helpers. In the freezer, the liquid starts to harden up at about -66°C. That puts it well into the liquid category at room temperature, letting you store it in simple bottles instead of pressure flasks. The vapor pressure counts, especially in warm rooms, adding risk if you don’t seal it tight or store it cool.
Safety Forces Careful Work
Safety data tells a seasoned handler not to skimp on gloves or goggles. That sharp odor was my first alarm, and skin contact or breathing it in can cause irritation or harm. The density and volatility mean spills spread quickly across benches. I once saw a hurried spill go racing toward the drain, forcing everyone to pause and break out the absorbent pads in a hurry. Fast action rules the day when working with heavy, volatile chemicals like this. A good chemical hood goes a long way toward keeping lungs clear and workspaces clean.
Making Something Useful Out of It
1-Bromo-2-chloroethane gives organic chemists an extra synthetic tool, supplying both a halogen source and a reactive substrate. The compound’s physical traits dictate how to handle and deploy it: heavy, organic-soluble, low-boiling. The bottle’s warning label and the cooling rack tell the real story. If you want to make cleaner, safer, or more efficient use of compounds like this one, pay close attention to these physical markers and store with respect. The chemistry will go smoother, the clean-up will shrink, and the stories about wild smells in the lab will fade away.


| Names | |
| Preferred IUPAC name | 2-Bromo-1-chloroethane |
| Other names |
Ethylene chlorobromide
Ethylene bromochloride Bromochloroethane 2-Chloroethyl bromide |
| Pronunciation | /waɪˈbrəʊməʊ tuː ˈklɔːrəʊˌiːθeɪn/ |
| Identifiers | |
| CAS Number | 107-04-0 |
| Beilstein Reference | 1209220 |
| ChEBI | CHEBI:41261 |
| ChEMBL | CHEMBL15668 |
| ChemSpider | 12177 |
| DrugBank | DB14006 |
| ECHA InfoCard | 03df16ac-c461-4681-b5fc-4b76b6630a89 |
| EC Number | 205-855-6 |
| Gmelin Reference | 9612 |
| KEGG | C19189 |
| MeSH | D001921 |
| PubChem CID | 6377 |
| RTECS number | KH8575000 |
| UNII | 8N4I9A836M |
| UN number | UN2520 |
| Properties | |
| Chemical formula | C2H4BrCl |
| Molar mass | 141.44 g/mol |
| Appearance | Colorless to yellow liquid |
| Odor | Sweet odor |
| Density | 1.353 g/mL at 25 °C (lit.) |
| Solubility in water | slightly soluble |
| log P | 1.83 |
| Vapor pressure | 1.6 kPa (at 20 °C) |
| Acidity (pKa) | 14.3 |
| Basicity (pKb) | 14.98 |
| Magnetic susceptibility (χ) | −7.96×10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.487 |
| Viscosity | 1.326 mPa·s (20 °C) |
| Dipole moment | 2.33 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 137.3 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -49.6 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -526.4 kJ/mol |
| Hazards | |
| GHS labelling | GHS02, GHS07 |
| Pictograms | GHS02, GHS07 |
| Signal word | Warning |
| Hazard statements | H302, H315, H319, H332, H411 |
| Precautionary statements | P210, P261, P301+P312, P305+P351+P338, P405, P501 |
| NFPA 704 (fire diamond) | 1-2-0 |
| Flash point | 43 °C (closed cup) |
| Autoignition temperature | 632°C |
| Explosive limits | Lower: 6.7% ; Upper: 14.4% |
| Lethal dose or concentration | Lethal dose or concentration: "LD50 (oral, rat): 1570 mg/kg |
| LD50 (median dose) | LD50 (median dose): 825 mg/kg (rat, oral) |
| NIOSH | PB6125000 |
| PEL (Permissible) | Not established |
| REL (Recommended) | REL = 1 ppm (5 mg/m³) |
| IDLH (Immediate danger) | 500 ppm |
| Related compounds | |
| Related compounds |
Ethylene dichloride
Ethylene dibromide 1,2-Dibromoethane Chloroethane Bromoethane 1,1-Dichloroethane 1,1-Dibromoethane 2-Bromoethanol 2-Chloroethanol |