Bromobenzene: From the Lab Bench to Modern Chemistry

Historical Development

Bromobenzene traces its roots back to the surge of organic chemistry in the mid-1800s. Early experiments relied on coal tar and basic glassware. Chemists like August Wilhelm von Hofmann studied aromatic compounds, leading to systematic halogenation of benzene derivatives. By the turn of the twentieth century, improved laboratory techniques made the production of pure bromobenzene more reliable and less hazardous. Over time, the compound transitioned from a mere curiosity to a standard tool in organic synthesis. What started as a labor-intensive process slowly grew into essential industrial technology. This evolution reflects not just a change in methods, but in the very mindset of chemical research: shifting from observation to precision, from small scale to mass production, and consistently integrating strict safety protocols.

Product Overview

Bromobenzene represents a fundamental aromatic halide with a single bromine atom bound to a benzene ring. Simple in structure, it supports an array of chemical syntheses in both industrial and academic settings. Its commercial forms range from analytical grade liquids to bulk volumes suited for manufacturing. Recognized largely for its role in Grignard reagent preparation, bromobenzene sees extensive use across pharmaceuticals, dyes, and laboratory research kits. The chemical’s straightforward molecular formula masks its versatility, acting both as a building block and a specialized reactant for more tailored synthesis. Handling this substance demands technical understanding, especially given its reactivity and potential health concerns.

Physical & Chemical Properties

Bromobenzene appears as a colorless to light yellow liquid at ambient temperature. It emits a faint aromatic odor that betrays its volatile nature. With a boiling point of roughly 156°C and a melting point near -30°C, bromobenzene remains stable under common laboratory conditions, but its vapor poses concerns in closed quarters. Measuring at a density of about 1.5 g/cm³, it sinks in water, demonstrating low solubility because the nonpolar benzene ring resists mixing with polar solvents. This liquid catches fire with enough heat, and its combustion yields nasty byproducts like hydrogen bromide. The molecular weight clocks in at 157.01 g/mol. On the chemical side, bromobenzene holds the benzene core largely intact, but the bromine atom opens doors for substitution reactions. Treatments with lithium, magnesium, or metals like iron unlock further synthetic potential.

Technical Specifications & Labeling

Bottles of bromobenzene leave the factory with a series of safeguards and details: purity levels, typical impurity thresholds, and storage guidelines all stamped on the label. Manufacturers frequently test for water content and residue levels below one percent, while spectroscopic analysis checks for any irregularities in aromatic structure. Regulatory compliance marks accompany safety icons that warn of both toxicity and flammability. UN identification codes, batch traceability, and expiration dates give end users a clear idea of handling and shelf life. These technical details rarely attract casual attention, but skipping any of them can introduce risk—either by degrading the product or introducing hidden hazards to a working environment.

Preparation Method

Most modern processes derive bromobenzene by direct bromination of benzene using elemental bromine in the presence of an iron catalyst. Iron filings or iron(III) bromide accelerate the substitution, pushing bromine to replace a hydrogen atom on the six-membered ring. The process generates hydrogen bromide as a byproduct, requiring careful venting and neutralization downstream. Strict temperature control avoids runaway reactions or multi-substituted products, which can muddy the final compound’s purity. Once the reaction completes, a series of extractions and distillations isolates the pure liquid. Older methods involved far more guesswork, often giving mixtures that demanded tedious separation. Today’s process, scaled for industry, balances yield, speed, and safety with ever-increasing efficiency.

Chemical Reactions & Modifications

Bromobenzene acts as more than a static molecule; its bromine atom primes the ring for a slew of synthetic possibilities. In the hands of a skilled chemist, bromobenzene forms Grignard reagents—a springboard into building complex carbon frameworks. Reactions with magnesium in dry ether convert bromobenzene to phenylmagnesium bromide, which then couples with carbonyl compounds. Other metal-halogen exchanges, particularly those using lithium, offer new routes to substituted aromatics. The aromatic ring itself undergoes nitration, sulfonation, and acylation, retaining the bromine’s influence on reaction orientation. Cross-coupling techniques like Suzuki and Heck reactions harness bromobenzene as a key reactant in forging biaryl structures, important in pharmaceutical and material science circles. Today’s chemical industry leans heavily on these advanced routes, pushing the limits of molecular construction.

Synonyms & Product Names

Over the decades, literature and industry catalogues have attached a variety of names to bromobenzene: monobromobenzene, phenyl bromide, and brombenzol all refer to the same chemical backbone. To avoid confusion during procurement or research, suppliers often cross-list these synonyms with standardized CAS numbers (CAS 108-86-1) and compliance codes. This robust naming system ensures traceability and product matching for high-stakes research or quality-driven manufacturing operations. Without clear naming and identification, even the savviest laboratory teams could waste resources chasing incorrect materials, risking both project timelines and research outcomes.

Safety & Operational Standards

Routine lab work with bromobenzene calls for gloves, goggles, and reliable ventilation. Vapors irritate the eyes and upper respiratory tract, causing discomfort or worse with concentrated exposure. Guidelines set by OSHA, NIOSH, and European agencies direct safe exposure limits, emphasizing containment during handling and proper waste disposal. Spills require absorption with inert materials and immediate cleanup. Technicians employ fume hoods to minimize inhalation hazards. Local exhaust systems and well-labeled storage cabinets line up as standard for facilities that stock this reagent. Ignoring these safeguards carries steep consequences: acute exposure brings headaches or malaise, and chronic mishandling could elevate the risk for organ damage.

Application Area

The reach of bromobenzene has grown well beyond its basic origins. Its role in synthesizing pharmaceutical intermediates underpins drug development pipelines worldwide. As a precursor, it helps piece together nonsteroidal anti-inflammatory drugs, sedatives, and antihistamines. Chemical plants use bromobenzene for agrochemical and dye production, capitalizing on its reactivity to introduce tailored aromatic systems. Researchers take it further: using bromobenzene in cross-coupling reactions to build novel organic semiconductors and advanced materials for next-gen electronics. Education plays a smaller but vital role; undergraduates tackle it in safe, guided experiments that set the stage for later, more sophisticated work. The ongoing versatility of bromobenzene keeps it central for anyone designing or building new molecules.

Research & Development

Cutting-edge labs tinker with new catalytic systems to make bromobenzene even more functional. Custom-modified catalysts target greener syntheses or clearer selectivity in chemical transformations. Recent work explores converting bromobenzene to value-added pharmaceuticals using milder, less wasteful conditions. Other efforts explore the use of flow chemistry to enhance safety and throughput during bromination—shifting away from bulky batch reactors and toward continuous processing. Machine learning and computational chemistry help predict how bromobenzene will behave under new conditions, guiding experiments before they ever reach the benchtop. Industry and academia alike keep tailoring both production and modification, chasing lower costs, gentler reactions, and a reduced ecological footprint.

Toxicity Research

Scientists and regulatory groups have mapped the risks of bromobenzene over generations. Acute exposure leads to drowsiness, headaches, or sometimes anemia—especially in poorly ventilated spaces. Animal studies show the compound metabolizes in the liver, forming reactive intermediates that can damage cells. Chronic contact, particularly by inhalation, may irritate the eyes, respiratory tract, and skin, while long-term overexposure threatens liver and kidney function. Early standards grew stricter with more data, pushing exposure limits downward. Regular monitoring and updated material safety data sheets help workers stay proactive. Labs rotate personnel and train newcomers with clear-eyed focus on personal protection.

Future Prospects

Developments in green chemistry hold promise for safer, more sustainable bromobenzene production. Emphasis now lies on minimizing toxic byproducts, finding benign solvents, and recycling catalyst materials wherever possible. Startups and chemical giants alike funnel resources into pilot plants running cleaner processes. On the research front, new cross-coupling paradigms expand what chemists can build starting from this familiar aromatic core. Digital tools make it easier to design entire reaction pathways in silico, trimming both time and risk involved in trial-and-error experimentation. For those of us who grew up with classic glassware and back-of-the-envelope calculations, it feels like the horizon keeps expanding, with bromobenzene’s utility only growing as creativity meets technical finesse.



What is Bromobenzene used for?

Understanding Bromobenzene’s Everyday Role

Bromobenzene doesn’t get flashy headlines. A quick look at its clear, nearly colorless liquid makes it seem boring. But it’s a vital tool on the chemistry bench, particularly for those working in pharmaceuticals, materials research, and education. Many folks may not realize this compound plays a behind-the-scenes part in developing products that touch daily life, from pain medicine to electronics.

The Building Block for Pharmaceutical Research

Pharmaceutical labs put bromobenzene to work every day. It’s a key stepping stone for synthesizing more complicated molecules, especially those used as building blocks in drug research. Imagine the painstaking process of creating hundreds of molecules to find just one that might help treat a chronic condition. Chemists need reliable starting points, and bromobenzene’s simple structure and reactive nature make it a popular pick. One job I had involved troubleshooting bottlenecks in drug synthesis. Our team leaned on bromobenzene because of its consistent behavior in reactions that add other groups to the benzene ring, a process called substitution.

Tools for The Organic Chemist

In undergrad chemistry labs, students meet bromobenzene early. It gives straightforward results in classic experiments, especially for teaching how to form carbon-carbon bonds. Suzuki and Grignard reactions use it as a starting material. These techniques let labs turn plain benzene into hundreds of useful chemicals, including ingredients for fragrances, agricultural chemicals, and high-strength plastics. Clear, repeatable results help students build confidence as they learn to think critically about procedures and outcomes.

Industrial Uses Beyond the Lab

Bromobenzene also moves out of small test tubes into industrial vats. Its role as a solvent draws less attention, but solvent quality can make or break an industrial process. Some companies use it during crystallization to help purify new compounds. Manufacturing sectors involved in dyes and flame retardants also call on bromobenzene for initial steps. Its higher density than water lets it act as a marker to test equipment that counts how fast liquids flow through industrial pipes—a trick familiar to many chemical engineers.

Health and Safety Up Front

No two ways about it: bromobenzene brings risks. Breathing in its vapors or getting it on your skin isn’t safe. Lab supervisors drill safety protocols over and over for good reason. Long-term exposure could harm the liver and kidneys. Responsible chemists double-check that fume hoods and gloves are used without fail. Learning to respect chemicals like bromobenzene makes a lasting impression—I remember fixing a spill in my early lab days, gloves slick and eyes stinging, realizing just how much routine safety matters. Regulations call for proper storage and disposal, ensuring this compound doesn’t end up where it shouldn’t.

Improving Safety and Sustainability

Much discussion now focuses on finding greener ways to do the same chemistry. Some researchers aim for alternatives that bring fewer environmental or health risks. Others adjust reaction conditions to use less solvent or make less waste. Support for this kind of work matters. It shows the chemical industry taking practical steps, not just talking, about reducing chemical hazards without sacrificing progress in making medicines or new materials.

Watching for What’s Next

Bromobenzene will likely anchor chemistry labs for years. Every time a student inches closer to a breakthrough or an industrial process goes off without a hitch, it’s clear that small, well-understood molecules like bromobenzene have earned their spot at the workbench. Paying attention to safety and cleaner chemistry can keep this resource available—for good use and with less risk.

What are the safety precautions when handling Bromobenzene?

Why Handling Bromobenzene Demands Caution

Bromobenzene looks simple enough—a colorless to pale yellow liquid, used in labs and industry for making other chemicals. After spending years in research labs, I’ve learned that simple substances often hide real risks under a calm surface. Bromobenzene doesn’t stand out with a strong smell or color, but it carries health hazards if you work too casually around it. Just a splash, a spill, or fumes can turn a routine task into an urgent medical situation.

Personal Protective Equipment: More Than a Formality

Nothing makes exposure to toxic chemicals memorable like the sharp sting of solvent on your bare hand. I still remember ignoring gloves once for “just a minute”—bad choice. Bromobenzene, in particular, absorbs through the skin and can cause everything from irritation to systemic poisoning. That’s why gloves—think nitrile or Viton—should go on before even opening the bottle. A proper lab coat, safety goggles, and closed shoes do more than tick a box; they stop splashes and fumes from finding skin and eyes.

Ventilation Isn’t Optional

Bromobenzene has a low boiling point and sends out vapors even at room temperature. Breathing those vapors never ends well. After meeting enough old-timers who spent years in poorly ventilated labs, I know what chronic chemical exposure can do—dizzy spells, chest pain, headaches. Ventilation in labs means more than cracks in windows. It calls for a well-maintained chemical fume hood, exhaust fans or air exchanges built for handling organic vapor.

Storage Really Does Make a Difference

Leaving containers out on a bench or piling them in a cabinet creates a recipe for broken bottles and leaks. Bromobenzene belongs in flammable liquid storage, far from direct sunlight and heat sources. Use shatter-resistant bottles with clear labeling. I’ve seen more than one costly cleanup follow a small leak that soaked into wood or drywall, which also creates a long-term health hazard.

Spill Response: Have a Plan

Relying on quick instincts can backfire during a spill. Bromobenzene, like many liquid organics, spreads fast and becomes airborne within seconds. It's smart to stock spill kits with chemical-neutral absorbents and to keep emergency showers and eye wash stations working. Evacuating at the first sign of a substantial spill saves lives and reduces injuries—calling professional responders isn’t overreacting. I’ve watched as poor planning led to a minor spill turning into chaos simply because nobody had practiced a simple procedure.

Medical Attention Isn’t Only for Obvious Symptoms

Not everyone reacts to chemicals the same way. I’ve known people who brushed off mild headaches or skin irritation, only to land in the emergency room by evening. With bromobenzene, even mild symptoms demand a visit to the medical office. Whether through the skin, lungs or mouth, exposure requires immediate flushing and professional assessment. The earlier the treatment, the better the outcome.

Building a Culture of Respect for Hazardous Chemicals

Safe handling starts long before you open a bottle. Training means more than signing off on an SOP—it means understanding exactly how things can go wrong and respecting those possibilities every single day. Encourage a culture where peers double-check gear, call out unsafe habits, and report every near-miss. In every workplace where I’ve seen this kind of attitude, injuries dropped and people got home safe.

Solid Safety Habits Protect Everyone

There’s nothing mysterious about working safely with bromobenzene—it comes down to respect, preparation, and refusing to cut corners. Each habit you build, from double-bagging waste to logging every use, adds up. The real goal isn’t just avoiding disaster, but making sure no one ever gets hurt in the first place.

What is the molecular formula and weight of Bromobenzene?

Getting Specific: The Numbers Behind Bromobenzene

Bromobenzene isn’t some exotic lab chemical reserved only for scientists in white coats. Anyone working with chemistry—even in simple workshops or classrooms—will probably run into it at one point. It’s a benzene ring with a single bromine atom swapped in for a hydrogen. That gives it a molecular formula of C6H5Br. Calculating the molecular weight means adding up the individual weights: carbon (12.01 g/mol), hydrogen (1.008 g/mol), and bromine (79.90 g/mol). Put those together, and the total molecular weight comes out to about 157.01 g/mol.

Why These Details Actually Matter in Real Life

Reading off formulas or weights from a data table can feel disconnected from hands-on chemistry, but knowing these numbers isn’t optional. Take lab safety as a top example. The exact formula and weight tell you how much of a substance you’re handling, help with calculating concentrations, and play a big part in making reactions predictable. One misstep with calculation, and you risk not just a failed experiment but a dangerous situation. I’ve seen more than one young lab partner get burned (sometimes literally) by not double-checking the details of their chemicals.

Beyond the classroom, these numbers start showing up in real applications, like the pharmaceutical and electronics industries. Bromobenzene’s structure makes it a prime candidate for making other useful compounds—essentially, it acts like a building block. In the creation of pharmaceuticals or dyes, efficiency depends on grasping the chemistry on this molecular level. A single error in the amount weighed out can lead to a dropped yield or contaminated product batch. Years ago, I watched a colleague spend a day troubleshooting a faulty synthesis, only to discover it came back to misreading a label’s molecular weight. Small mistakes snowball.

Looking At the Bigger Picture: Beyond Textbook Chemistry

Bromobenzene also brings environmental and safety questions into the spotlight. The more you know about a chemical’s makeup, the better equipped you are to deal with spills or disposal. Authorities in many countries keep close eye on substances like this due to toxicity and flammability risks. Environmental chemists, for example, use exact data like molecular weight and formula when setting rules for waste handling. Lax attitudes put workers, students, and communities at risk. Learning the facts cuts straight through misinformation and exposes reckless shortcuts.

Accurate chemical data has a habit of trickling outward, touching everything from school laboratories to massive production plants. Knowledge gets passed along: students call out instructors when numbers don’t add up, apprentices catch mistakes before scale-ups in industrial settings. A friend of mine, years into his chemical engineering job, told me the difference between a careless and careful company often traces back to the small stuff—like how seriously they treat a label reading C6H5Br, 157.01 g/mol.

There’s a lesson built into each bottle on the shelf: pay attention to the technical details, and you’ll not only keep people safe—you’ll make the science more effective. It doesn’t take much to get off track, but it only takes a little diligence to keep everything running smoothly.

Is Bromobenzene hazardous to health or the environment?

Why Bromobenzene Draws Scrutiny

Bromobenzene often pops up in chemical manufacturing labs and serves as a building block in organic chemistry. At first glance, this colorless liquid doesn’t sound all that menacing, but science and experience paint a different picture. Inhaling its vapors gives off that unmistakable almond scent, and from working in research labs, I learned to treat such smells as warnings, not quirks. Each time a bottle of bromobenzene shows up in the workplace, it comes with the promise of utility—and a red flag for personal safety.

Health Hazards Rise from Exposure

People who handle bromobenzene without proper safety steps put themselves at risk. Inhaling or touching the liquid can irritate skin, eyes, and internal organs. Exposure in confined spaces may cause dizziness and headaches, and repeated contact starts to worry even the most skilled chemists. Lab accidents rarely get media attention, but the repercussions for workers are real. CDC reports show that bromobenzene can damage the liver and central nervous system if exposure becomes routine. Most ordinary folks don’t cross paths with this chemical, but neglect at the workplace sabotages health and peace of mind for chemists, plant workers, and anyone dealing with production or transport.

Environmental Stakes

Bromobenzene rarely enters waterways or neighborhoods straight from the bottle. The risk grows once it escapes through spills or irresponsible disposal. I’ve seen enough stories about poorly maintained storage tanks and leaks to know that even a small slip can poison fish and stunt aquatic life. Bromobenzene breaks down slowly in the environment. That means contamination lingers, moving through soil, water, and even the air. Plants can absorb residues through their roots, and traces make their way up the food chain. In 2022, studies by environmental groups highlighted the persistence of brominated organics in sediment near chemical plants. This evidence isn’t background noise; it speaks to a pattern where industrial accidents leave lasting scars.

Managing the Dangers

The best labs operate under rules that treat chemicals like bromobenzene with the seriousness they deserve. Regular training, air-tight storage, and proper ventilation cut down exposure and accidents. Personal experience taught me the value of everyday rituals—like gloves, goggles, and regular monitoring—over fancy gear that looks impressive but collects dust. The simple habits stack up to create safer workspaces. OSHA and EPA rules step in as watchdogs, setting limits on how much exposure workers can face in an eight-hour shift and how much waste can leave a facility.

Cleanup rules need teeth. Dumping leftover bromobenzene down the drain may save a few minutes, but it costs communities and ecosystems in the long run. Instead, companies must recycle solvents when possible and destroy residues with approved methods. Investing in safer substitutes pays off for future workers and neighborhoods nearby. Chemists and managers shape the story every day with the choices they make. Clear labels, emergency plans, and transparent reporting create a culture where safety gets attention.

The Value of Informed Handling

Bromobenzene doesn’t belong in kitchens, backyards, or unmarked warehouses. The right approach checks hazards before they snowball. Workers, managers, and regulators help each other out by taking safety reminders seriously. Fact-based choices and ongoing respect for the risks support not only healthy workers but cleaner neighborhoods and stronger ecosystems.

How should Bromobenzene be stored and disposed of?

Bromobenzene Risks Demand Careful Handling

Bromobenzene, a clear liquid used in labs and industry, brings some real risks to the table. Breathing its fumes irritates the airways, and even a little on the skin can cause rashes or burning. With enough exposure, the chemical harms vital organs like the liver and kidneys. For that reason, proper storage and disposal don’t just check a box—they protect people who handle it, folks nearby, and the wider environment.

Keeping Bromobenzene Secure

If you pop the lid on a bottle of this stuff, a strong mothball smell hits fast. That tells you right away that it evaporates quickly. A tight-fitting cap stops vapor leaks and accidental spills. The bottle stands best in a cool room, far from sunlight and heated surfaces. If the liquid gets too warm, pressure builds up in the bottle. I learned early in the lab not to stash chemicals near radiators or windows for this reason; a little laziness can turn into a toxic mess overnight.

Bromobenzene reacts with strong acids, bases, and oxidizing agents. Keeping it away from bleach, nitric acid, and other chemicals with a history of violent reactions avoids dangerous accidents. I’ve seen close calls at research benches where a single misplaced bottle led to hours of emergency cleanup. Flammable storage cabinets, made from metal or flame-resistant plastic, offer the kind of extra safeguard that makes all the difference. These cabinets help slow the spread of fire, buying time for folks to evacuate if something goes wrong.

Every container deserves a clear, robust label. The best labels include the chemical name, hazard warnings, and emergency info. In my teaching years, I saw new lab students reach for the wrong reagent more times than I care to count. Strong labeling stops confusion before it starts.

Safe Disposal Keeps Harm Out of the Water and Soil

Pouring excess bromobenzene down the drain or throwing it in the regular trash looks easy, but that shortcut poisons water systems and harms wildlife. In the past, lax disposal rules led to places with undrinkable water and blighted land no one wanted. The damage lingers for decades.

The right way means working with a licensed chemical disposal service. These pros use sealed drums and follow rules meant to limit harm at every step. If a facility generates large amounts of waste, rules from agencies like the EPA lay out how to track every drop from the lab to the disposal site. Smaller lots, like those from hobbyists or schools, can often be dropped off at hazardous waste collection events. I remember joining student groups hauling out boxes for one of these pickups—the peace of mind comes from doing it right.

Spills get cleaned up with absorbent pads and plenty of ventilation, then the pads are sealed in a labeled, chemical-resistant bag. No one wants to risk a janitor picking up mystery rags from the trash. Even the gloves used during cleanup need their own bag. Quality disposal isn’t glamorous and takes effort, but it keeps toxic compounds where they belong.

Transparency Builds Trust

Storing and disposing of chemicals like bromobenzene is more than a technical process. It’s about showing respect—to coworkers, to neighbors, to the planet itself. Sharing hazard data openly, following proven protocols, and seeking advice from local experts or regulators pays off. As more people learn and share the best ways to handle these materials, fewer accidents and environmental issues crop up.

Bromobenzene
Bromobenzene
Bromobenzene
Names
Preferred IUPAC name Bromobenzene
Other names Monobromobenzene
Phenyl bromide
Brombenzene
Pronunciation /ˌbrəʊ.moʊˈbɛn.ziːn/
Identifiers
CAS Number 108-86-1
Beilstein Reference 1361166
ChEBI CHEBI:17563
ChEMBL CHEMBL1079
ChemSpider 1026
DrugBank DB04210
ECHA InfoCard 100.027.860
EC Number 601-025-00-5
Gmelin Reference 1360
KEGG C01449
MeSH D001930
PubChem CID 241
RTECS number CY1400000
UNII YOW8V9698H
UN number UN2515
CompTox Dashboard (EPA) DTXSID7020152
Properties
Chemical formula C6H5Br
Molar mass 157.01 g/mol
Appearance Colorless to pale yellow liquid
Odor Aromatic
Density 1.495 g/mL at 25 °C (lit.)
Solubility in water 0.40 g/L (20 °C)
log P 3.3
Vapor pressure 4.18 mmHg (25°C)
Acidity (pKa) ~43
Basicity (pKb) 12.7
Magnetic susceptibility (χ) -81.5·10⁻⁶ cm³/mol
Refractive index (nD) 1.558
Viscosity 0.806 cP (20°C)
Dipole moment 1.72 D
Thermochemistry
Std molar entropy (S⦵298) 87.0 J⋅mol⁻¹⋅K⁻¹
Std enthalpy of formation (ΔfH⦵298) (-7.0) kJ·mol⁻¹
Std enthalpy of combustion (ΔcH⦵298) -3225.9 kJ/mol
Hazards
GHS labelling GHS02, GHS07
Pictograms GHS02,GHS07
Signal word Warning
Hazard statements H226, H315, H319, H335
Precautionary statements P210, P261, P280, P301+P312, P303+P361+P353, P304+P340, P305+P351+P338, P405, P501
NFPA 704 (fire diamond) 2-2-0
Flash point 58°C
Autoignition temperature 503°C
Explosive limits Upper: 5.4%, Lower: 1.4%
Lethal dose or concentration LD50 oral rat 3,140 mg/kg
LD50 (median dose) LD50 (median dose): 3160 mg/kg (oral, rat)
NIOSH CN1400000
PEL (Permissible) Not established
REL (Recommended) 2 ppm
IDLH (Immediate danger) 1000 ppm
Related compounds
Related compounds Benzene
Fluorobenzene
Chlorobenzene
Iodobenzene
Phenol
Nitrobenzene