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Fluorobenzene: A Down-to-Earth Look at an Unsung Workhorse

Historical Development

Back in the 1800s, organic chemists learned how to slip a fluorine atom onto a simple benzene ring—the birth of fluorobenzene. At the time, synthetic organic chemistry was like the Wild West. Most efforts went to toluene and aniline, but as curiosity about new ring structures grew, chemical pioneers found ways to swap out hydrogens on benzene for all sorts of things, including fluorine. Fluorobenzene didn’t kick off an industrial frenzy but quietly settled into labs and industry circles. Decades before “specialty chemicals” became buzzwords, this compound showed up in reference texts and chemical supply house catalogs. Chemists realized, through repeated experiments and a lot of glassware cleaning, just how useful this molecule could be as a stepping stone, a solvent, or a probe when mapping out how aromatic rings behave with halogen substitution. That quirky blend of being reactive enough for chemistry but safe enough to handle in modest quantities put it in a unique spot throughout the 20th century.

Product Overview

Fluorobenzene often sits in the shadow of flashier chemicals. It comes as a colorless, oily liquid with a faint, characteristic odor. Some people won’t even notice a whiff, but lab veterans recognize it straight away. It’s not considered exotic today, but that unobtrusive profile means it gets plenty of use without much fanfare. It slips into the role of a solvent for a few high-value reactions, shows up as an intermediate on the long path from raw petrochemicals to advanced polymers, and helps researchers probe the effects of fluorine atoms on aromatic systems. The small molecular tweak—just one fluorine replacing a single hydrogen—leads to properties different from both benzene and other aromatic halides, giving it a unique signature.

Physical and Chemical Properties

This compound boils at about 85°C, lower than plain benzene and close enough to toluene to make separation a detail-oriented job. It doesn’t freeze until the temperature drops to -44°C, so storage in ordinary labs or warehouses works for most climates. Its density checks in a little heavier than water, but it won’t sink in an organic mixture. That lone fluorine atom tweaks the electron cloud of the ring, pulling in electrons more than hydrogen but not as aggressively as chlorine. Chemists studying aromatic substitution notice the fluorine directs new groups onto the ring’s meta positions, a trick that can help synthesize multi-substituted aromatics with more precision. It stands up to mild acids and bases and keeps its structure in the face of weak oxidizers, but strong nucleophiles like alkoxides can poke holes in the molecule’s stability.

Technical Specifications and Labeling

Handling a chemical like fluorobenzene means paying attention to safety standards, purity, and accurate labeling. Standard supply bottles list purity by gas chromatography, and concentrations above 99 percent rank as “analytical grade.” Health and safety labels flag the moderate toxicity, potential for irritating the eyes and lungs, and fair flammability risk, matching what you’d expect from a volatile aromatic. Flammability sits at the lower end among aromatic halides, but with the right spark, vapors catch fire. No one uses it without a working fume hood and gloves. Proper labeling spells out the basic first-aid steps for spills and contact, matching the standards from groups like OSHA and GHS. As modern regulations update hazard pictograms, these tags show up on every bottle shipped around the world, which helps cut down on lab mishaps.

Preparation Method

Early research delivered fluorobenzene through brute force: reacting benzene with fluorine itself, in the presence of iron or copper catalysts. This method wasn’t gentle, and safety equipment in the 1930s looked a lot different. More refined routes came along, letting chemists use milder reagents like silver(I) fluoride or by relying on halogen exchange—swapping a chlorine on chlorobenzene for a fluorine in the lab. That approach, known as halex or halide exchange, dropped the danger and opened up scalable, reliable fluorobenzene for bulk applications. Commercial production today follows these improved routes, keeping yields high and byproducts low, a big deal for both environmental standards and the bottom line.

Chemical Reactions and Modifications

Fluorobenzene serves as a versatile building block for making more specialized molecules. The ring resists attack from many nucleophiles, but that fluorine directs further reactions in a predictable way. Chemists interested in synthesizing pharmaceuticals or specialty polymers often use it as a template molecule. Electrophilic aromatic substitution is predictably altered compared with benzene—nitration, sulfonation, or Friedel-Crafts alkylation happen slower, but you get better control over the placement of new groups. A good trick is using fluorobenzene to block or guide the action on the ring, then removing or further modifying the fluorine as needed with other reagents down the road. That unique combination of stability and reactivity means it doesn’t just vanish into a flask and get forgotten—it really can set the stage for making newer, more useful molecules.

Synonyms and Product Names

Scan a chemical catalog or academic journal, and you see fluorobenzene show up under a couple of aliases. People call it monofluorobenzene, phenyl fluoride, or just the obvious, fluorobenzene. These aren’t marketing tricks, just historical artifacts born from different traditions in organic nomenclature. Whether you call it by its IUPAC name, its systematic label, or an older common name, the content stays the same. The practical impact comes in academic databases or regulatory filings, where missing a synonym can cost hours or cause shipment delays.

Safety and Operational Standards

Running a process or lab experiment with fluorobenzene isn’t risky if the right precautions stay in place. Anyone who’s spent time in an organic lab knows that keeping these aromatics away from sparks and open flames counts for a lot. Inhalation risk is moderate, so ventilation plays a lead role. Gloves and goggles are standard, but splash incidents are rare with reasonable care. Industry guidelines set occupational exposure limits and recommend action when airborne concentrations edge upward, but day-to-day, careful technique and air circulation rule out most harm. Waste disposal can’t be casual, since aromatic halides resist breaking down in the environment, so collection protocols and incineration in approved facilities avoid long-term contamination. Training workers and lab staff in up-to-date safety standards pays off both in regulatory compliance and in keeping people confident when handling the chemical.

Application Area

Fluorobenzene doesn’t fight for headlines, but it quietly supports plenty of modern technologies. Its main role lands in the chemical industry as a building block for pharmaceutical intermediates, agrochemicals, and advanced materials. Companies synthesize other fluorinated aromatics from it, which show up in drugs, industrial solvents, and high-performance plastics. Research labs use it as an NMR standard for calibrating equipment or to trace reaction mechanisms involving halogenation. A few niche uses turn up in electronics and specialty coatings, where developers care about chemical resistance and precise behavior. Even if demand never matches that of bulk solvents or feedstocks, its unique mix of reactivity, safety, and specialty roles earns it a permanent spot on chemical order sheets around the world.

Research and Development

R&D has never stopped probing what fluorobenzene and its derivatives can offer. In my own research days, I saw how the scientific community values “simple” halogenated aromatics—they help test new catalyst systems, or decode how drugs bind to proteins. Chemoinformatics models keep absorbing more data on its reaction kinetics, toxicity, and substituent effects. Chemical suppliers experiment with greener, more energy-efficient routes for making it, especially as pressure rises to shrink halogenated waste. Academic labs examine fluorobenzene side by side with its heavier relatives like chlorobenzene and bromobenzene, mapping out trends in how halogens tweak physical behavior and electronic properties. For anyone teaching organic chemistry, it makes a reliable case study in fluorine’s subtle but important effects on aromatics.

Toxicity Research

Historical reports and new studies agree on a few things: fluorobenzene can irritate lungs and skin, and at high doses it causes central nervous system symptoms, but acute poisoning isn’t common in occupational settings with good safety habits. Researchers in toxicology show that its volatility poses a greater risk than long-term accumulation, since the body tends to excrete simple aromatic halides. Animal models help fill in the gaps on chronic exposure, with most signaling low bioaccumulation but potential trouble at very high, repeated doses. From a regulatory side, emissions into water or air meet strict caps, given both the persistence of aromatic rings and the environmental caution surrounding fluorinated organics in general. That steady push for safer handling and deeper research into metabolites drives tighter guidelines every decade.

Future Prospects

Fluorobenzene may not launch a revolution, but it keeps finding new jobs. As pharmaceutical companies chase drugs that need fine-tuned chemical properties, fluorinated molecules grab attention. This compound’s reactivity profile, predictable substitution pattern, and ability to serve as a precursor for more complex molecules mean its production isn’t going to disappear. On the energy and environment front, new methods cut down on hazardous byproducts, giving synthetic chemists peace of mind. With ongoing demand for ever-purer specialty chemicals and the pressure to limit waste, advances in catalytic halide exchange and bio-inspired synthetic techniques stand ready to reshape how companies make and use it. Every time industry reaches for new materials with better thermal tolerance, chemical resistance, or pharmacological profiles, that simple little molecule gets called off the bench, once again proving its worth—and forcing the rest of us to pay it a bit more respect.




What is Fluorobenzene used for?

Unpacking a Common Industrial Chemical

Fluorobenzene doesn’t get much attention outside of chemical plants or research labs, but it plays a quiet and important role in a range of industries. If you spend much time around industrial chemists, you hear this substance crop up as a common mention, often tucked into a laundry list of intermediates. Its main job centers on being a building block for bigger, more complicated molecules—many of which end up in things we encounter every day.

Foundation for Pharmaceuticals and New Chemicals

In medicine and drug manufacture, tweaking a molecule’s chemical structure can mean a world of difference for how a drug behaves. Fluorobenzene offers a simple, reliable way to get a fluorine atom onto a molecule’s framework. This little change can help medicines last longer in the body or find their target cells faster. Drugs for cancer and neurological diseases sometimes pull fluorobenzene into the early steps of their development.

Chemists often rely on fluorobenzene to help make other, more exotic, chemical intermediates. It acts as a kind of molecular Lego block, sitting at a point where new pieces get snapped on, or pieces are swapped out. I’ve watched researchers run their hands over reaction plans, picking fluorobenzene for its stability and the way it avoids reacting with side ingredients unless told to.

Role in Agrochemicals and Pesticides

Moving away from medicine, the world of agriculture counts on fluorobenzene for a less obvious reason. Its structure lets it serve as a base for certain herbicides and fungicides. Getting the right chemical properties into pest control agents sometimes calls for that stable, aromatic core. Companies chase higher crop yields but also battle resistant weeds. Here, fluorinated compounds give them one more option to test when older products lose ground.

Material Science and Specialty Polymers

Material scientists lean on chemicals like fluorobenzene for a different set of reasons. Some cutting-edge plastics and advanced coatings use derivatives that come from fluorobenzene’s basic shape. You’ll find these materials in electronics, in components exposed to heat or friction, or anywhere industry wants something tough and chemically brave.

Personal experience in a university chemistry lab taught me how tricky some of these syntheses can get. Simply plugging a fluorine atom onto a benzene ring isn’t easy. Many attempts end up with messy mixtures or useless byproducts. Fluorobenzene shortcuts this hassle, allowing faster progress in creating high-purity samples.

Risks, Handling, and Looking Ahead

Like many industrial chemicals, fluorobenzene brings health and safety concerns. It can irritate skin and eyes, and inhaling it over time affects the nervous system. Responsible chemical handling means gloves, goggles, and good ventilation. Many companies invest in better tracking, ventilation, and training to avoid spills or accidental exposure.

As demand for pharmaceuticals and specialized materials rises, more attention falls on sustainable ways to produce fluorobenzene. Green chemistry teams now focus on better catalysts and cleaner processes. Their hope is to limit waste and use less energy, especially as environmental rules tighten around chemical manufacturing.

Why It Matters

Fluorobenzene often hides behind the curtain, but its presence makes a difference across several major sectors. Whether it’s enabling medical breakthroughs or creating materials that last, it underpins advances that touch daily life—even if few outside science circles notice. Choosing chemicals responsibly and pushing for cleaner production give us an edge in balancing progress with health and safety.

What are the safety precautions when handling Fluorobenzene?

The Real Dangers of Fluorobenzene

Fluorobenzene looks and smells pretty innocuous, but don't let that fool you. This stuff comes from the chemical family used to make pharmaceuticals and pesticides, which means it's strong and potentially harmful. Breathing in the vapor, even in small amounts, can leave you with headaches, dizziness, or nausea. Getting any on your skin might not seem like a big deal at first, but it dries you out fast and can lead to rashes or cracking. Eyes are even more sensitive — any splash needs fast attention.

Protecting Yourself: Lessons from the Lab

I’ve spent years working around all kinds of chemicals, and the number one rule never changes: good personal protective equipment. Don’t cut corners. Always wear well-fitted gloves, a lab coat, and splash-proof goggles. If the job calls for it, use a face shield so you don’t end up with a ruined day because of a stray droplet. If you ever spill any, make sure to use the right chemical-resistant gloves — not the cheap disposable ones. Fluorobenzene can break right through certain glove materials, leaving your skin exposed. The right information about compatibility keeps you a step ahead.

Ventilation and Air Quality Checks

No matter how careful you are, you can’t see vapor buildup happening. Closed rooms and fume-free hoods don’t mix. Every responsible workplace, from university labs to big chemical factories, puts cash into proper ventilation systems and checks airflow regularly. If your vent hood doesn’t pull hard enough, walk away until it gets fixed — no experiment is worth risking your lungs. Monitoring the air keeps small leaks from flying under the radar.

Don’t Play Fast and Loose with Storage

Fluorobenzene is flammable. You drop a container, splash some on the bench, or get careless around an open flame, and things can go south in seconds. Always seal bottles tightly and store them in approved chemical cabinets, well away from oxidizers and heat sources. Even in smaller labs, check those cabinets a few times a month for leaks or cracked bottles. One forgotten spill or an unnoticed vapor build-up creates a bad memory fast.

Cleanup Isn’t Just "Wipe and Go"

After a spill, grab spill pads and the right containers. Skip the paper towels. Most places have detailed chemical hygiene plans that cover exactly how to clean up — and if they don’t, someone needs to make one. Collect all waste in a dedicated container labeled clearly, since mixing waste can cause bigger headaches.

Staying Ahead with Training

Every year, someone new joins our team, eager but green. Before they ever handle a bottle, they go through hands-on safety drills: learning how to work with spill kits, read chemical labels, and react to hazardous exposures. That knowledge sticks much better than just reading a poster. Good training transforms nervous newcomers into careful, competent colleagues.

Simplicity and Consistency Save Lives

The truth is, solid chemistry practices don’t need to be flashy. Well-chosen protective clothing, clean workspaces, working air systems, and reliable storage add up. It’s the basics, repeated with no shortcuts. Everyone deserves to go home safe at the end of the day — and with stubborn chemicals like fluorobenzene, that mindset really shows its value.

What is the chemical formula of Fluorobenzene?

Understanding Fluorobenzene: More Than Just a Formula

Ask a chemist about fluorobenzene and you’ll hear the formula: C6H5F. Six carbon atoms ring together, five hydrogens hang off like branches, and a single fluorine claims a spot, elbowing out what would have been a sixth hydrogen. That’s all it takes for benzene, an old face in chemistry, to morph into something quite different—just one swap, one fluorine.

Why Fluorine Changes Everything

My own encounter with fluorobenzene was in a research lab, tucked in the corner of an industrial chemistry building. The odor hit sharp and sweet, surprising considering how dangerous benzene, its close relative, is to breathe. With one fluorine, the molecule becomes more stable against breaking down, but it also turns less reactive. That matters in medicine, agriculture, and electronics, where stability and predictability help keep things clean and efficient.

Fluorine packs a punch. Its small size belies how much it can change a chemical’s behavior. Swap out a hydrogen for fluorine, and you get a molecule ready to handle heat or light, less likely to degrade, harder for bacteria to chew up. That’s made fluorobenzene a choice starting point for making drugs or pesticides that need to last—sometimes longer than they should.

Safety, Environment, and Responsibility

Fluorobenzene doesn’t just disappear after it’s made. In factories, each gram needs careful handling. Spills or leaks, even in small amounts, can move fast through soil and water. Regulations across Europe and North America now push companies to capture or neutralize waste, but rules only work when people have training and enough resources to stick to them. My time working with chemical disposal teams showed me how corners get cut to save a few dollars, especially at small or understaffed operations.

Long-lasting chemicals bring long-term consequences. Fluorine-containing compounds build up in places nobody expected: rivers, animal tissue, even breast milk. That’s why researchers push for safer alternatives—green chemistry, fresh thinking on molecule design, and more investment in research. Instead of simply swapping in fluorine to boost performance, labs now look at how molecules break down after being used and what that breakdown means for living things.

Solutions Come from People, Not Just Science

Tough rules and watchdog agencies help, but the biggest difference comes from engineers, plant workers, and researchers who take time to double-check valves, update process manuals, and ask hard questions about waste. I watched colleagues save thousands of liters of water by retooling a cleaning step, with no high-tech gadget or million-dollar grant. Giving people room to try new safety routines or adapt cleaner chemistry can sometimes do more than any single breakthrough.

The Next Chapter for Fluorobenzene

Every new material comes with risks alongside benefits. The chemical formula C6H5F stands for more than atoms locked in a ring—it signals the challenge of balancing progress and safety, using knowledge not just for profit but for protection. If anything, working with molecules like fluorobenzene taught me that even basic chemistry can shape the air we breathe, the water we drink, and the future we leave for others.

How should Fluorobenzene be stored?

Why Storage Isn’t Just About Shelf Space

Anytime someone brings fluorobenzene into a workplace, safety has to get more attention than convenience. I remember the day a drum of chemicals arrived at our local lab, and the label read “Flammable—Keep Away From Heat.” Nobody ignores those words, especially not after hearing stories of old labs that caught fire from someone leaving a volatile compound near a radiator. Fluorobenzene isn’t just another bottle on the chemical shelf; it brings its own set of demands.

Room Temperature Isn’t Always Right

Left sitting out, fluorobenzene will evaporate into the air. The smell might even bring you back to high school chemistry, but this isn’t harmless. The compound could irritate eyes and skin and nobody wants to risk breathing it daily. So smart storage starts with a cool, well-ventilated spot, under lock and key. That keeps fumes from building up and people from stumbling onto it by mistake. Good air flow beats headaches, both literally and for insurance paperwork.

Fire Hazards Are Real

Check the flash point: fluorobenzene will ignite at 48°C (about 118°F). In a facility that stores anything flammable, that’s no laughing matter. One mistake—like keeping the container close to a hot lamp or near a heating vent—can spread flames fast. I’ve worked in places where a simple chemical spill, because of poor storage habits, brought in first responders and shut down work for days. Proper storage calls for a flammable liquids cabinet, grounded against static. Metal cans or tightly sealed glass bottles work best. No one reaches for “just any shelf” if they know the risks.

Corrosion and Labels Matter

Fluorobenzene eats at some plastics and rubber. I’ve pulled corroded gaskets off leaky containers and seen how fast a bad seal can turn a safe room into a hazard. Always keep this chemical in approved containers—usually amber glass does the trick. Labels need to stay visible and accurate. I once saw a faded marker scrawl cause confusion with another clear liquid; better to take five minutes for new labels than gamble on a dangerous mix-up.

Why Training Shouldn’t Stop

People get comfortable and forget rules. It happens after a long week or late hours. There was a time I found a new intern moving chemicals without gloves or goggles, not out of recklessness, but because nobody explained the risks again lately. Refreshers save skin and careers. OSHA and national guidelines offer clear steps; too many folks forget to read or share them.

What Works for Handling Spills

Absorbent pads, sand, or vermiculite can help in a pinch. I once watched someone try to mop up a spill using paper towels, only to spread the problem. Special spill kits tucked near storage areas are the right move. Fast cleanup, clear communication, and direct lines to emergency support make a difference. It pays off to practice these routines before facing a real spill.

Better Planning, Fewer Accidents

Good habits cut incidents before they start: clear labeling, a flammable cabinet, regular training. These sound like simple steps, but too often shortcuts lead to reports nobody wants to write. My experience says all chemicals ask for respect, and fluorobenzene ranks near the top for care. Safe storage isn’t about paranoia—it’s about sending everyone home healthy at the end of the day.

What are the potential health effects of exposure to Fluorobenzene?

What Happens With Fluorobenzene Exposure?

Fluorobenzene is a chemical that doesn’t make headlines every day, but it makes its way into labs, manufacturing spaces, and some specialty products. Anyone working around solvents or certain chemical processes might cross paths with it. Folks who haven’t given it much thought may feel it belongs in the distant world of chemical plants, but exposure isn't as far-removed as you'd think. Workers and their families deserve to know what repeated exposure can bring, not just a list of symptoms from a textbook.

Researchers who have handled the stuff describe a sharp, sweet odor and notice at once it gets right into the head through breathing. Inhaling the vapor—especially in places without enough ventilation—can bring dizziness and headaches in a hurry. Sometimes, it's easy to brush off the first symptoms as “one of those days.” Ongoing contact doesn’t just annoy the senses. Over time, fluorobenzene acts as a central nervous system depressant. That spells out possible memory lapses, trouble keeping focus, and tremors that might not go away right after you leave work. Nausea and nose or throat irritation usually kick in early, even with short stints in a poorly-aired room.

Bringing the Facts

Data from the Agency for Toxic Substances and Disease Registry show that animals exposed to moderate or high levels started to lose weight, and researchers found liver and kidney changes. The human body doesn’t shrug off this chemical overnight. Metabolites stick around a while, and the body’s filter organs—liver and kidneys—take the main hit. Longer-term exposure raises red flags for organ health. Worldwide safety guidelines from organizations like OSHA put exposure limits in place, aiming to keep levels far below what damages factory animals. Still, not every workspace takes the same care, and not every worker knows how to get the right information.

I’ve seen firsthand how “just a little solvent” lingers on the mind after the day ends, especially among those not trained to spot chemical symptoms. Teams joke about “lab headaches” as if they’re just the price of the job. No one wears pain or fogginess for long without consequences. Many smaller businesses skip routine air quality checks, believing big symptoms won’t hit their shop. Years later, chronic fatigue and memory problems don’t have neon warning signs that point back to exposure.

Practical Steps Forward

Solutions don’t come easy, but clear air and good habits in the workspace protect more than company profits. Every workplace dealing with fluorobenzene ought to keep updated material safety data sheets where anyone can spot and read them. Proper ventilation isn’t an option—it’s a requirement for any place that handles volatile chemicals. Simple air filters won’t cut it. Closed systems and local exhaust fans set close to the source make a big difference. Don’t let protective gear like gloves and respirators collect dust; regular training and real-world drills save both health and trouble later.

People need the right to ask pointed questions about what they’re breathing and touching, with no corporate jargon to hide real dangers. Health monitoring—blood or urine tests for those who work with solvents regularly—should not be a rare offering. If someone feels “off” at work more often than not, that’s worth a second, even third look. Employers and regulators need to listen instead of brushing off concerns. In communities close to factories and labs, keeping neighbors informed about air testing and potential leaks is not just ethical—it builds trust and keeps everyone a little safer.

Fluorobenzene
Fluorobenzene
Fluorobenzene
Names
Preferred IUPAC name Phenylium fluoride
Other names Monofluorobenzene
Phenyl fluoride
Benzene, fluoro-
1-Fluorobenzene
Pronunciation /ˌfluː.ə.rəʊˈbɛn.ziːn/
Identifiers
CAS Number 462-06-6
3D model (JSmol) `C1=CC=C(C=C1)F`
Beilstein Reference 1209243
ChEBI CHEBI:5079
ChEMBL CHEMBL14224
ChemSpider 5797
DrugBank DB01837
ECHA InfoCard 03bbddc7-3e3b-410b-9c09-b90de7233e01
EC Number EC 203-692-4
Gmelin Reference 143079
KEGG C01370
MeSH D005434
PubChem CID 7964
RTECS number CU1400000
UNII S2A7J0XZU5
UN number UN2386
CompTox Dashboard (EPA) DTXSID3023723
Properties
Chemical formula C6H5F
Molar mass 96.102 g/mol
Appearance Colorless liquid
Odor Aromatic odor
Density 1.02 g/mL at 25 °C (lit.)
Solubility in water 1.0 g/L (20 °C)
log P 2.76
Vapor pressure 9.6 mmHg (20°C)
Acidity (pKa) 31.0
Basicity (pKb) -13.0
Magnetic susceptibility (χ) -74.6·10⁻⁶ cm³/mol
Refractive index (nD) nD 1.460
Viscosity 0.812 mPa·s
Dipole moment 1.60 D
Thermochemistry
Std molar entropy (S⦵298) 111.2 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) −106.2 kJ·mol⁻¹
Std enthalpy of combustion (ΔcH⦵298) -2855.0 kJ·mol⁻¹
Hazards
GHS labelling GHS02, GHS07
Pictograms GHS02,GHS07
Signal word Warning
Hazard statements H226, H332, H312, H315, H319
Precautionary statements P210, P261, P280, P301+P310, P304+P340, P312, P330, P403+P233, P501
Flash point +32 °C
Autoignition temperature 560°C
Explosive limits Explosive limits: 1.1–7.6%
Lethal dose or concentration LD50 oral rat 3000 mg/kg
LD50 (median dose) LD50 (median dose): 300 mg/kg (oral, rat)
NIOSH NIOSH: CU6475000
PEL (Permissible) 1 ppm (8-hour TWA)
REL (Recommended) 1 ppm (8-hour TWA)
IDLH (Immediate danger) 200 ppm
Related compounds
Related compounds Chlorobenzene
Bromobenzene
Iodobenzene
Nitrobenzene
Aniline
Benzene
Toluene