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3-Chlorophenol: Looking Deeper at a Chemical’s Past, Present, and Future

Historical Roots and Product Landscape

3-Chlorophenol grew out of early work in organic chemistry, back when scientists tried to understand what happened if you swapped atoms on the benzene ring. Its story, spanning from the crowded chemical plants of the 19th century to today's research labs, reveals how industrial chemistry shapes earthly life. This compound started as an offshoot in the refining process for phenolic products, often turned out as an intermediate during the manufacture of pesticides, antiseptics, and pharmaceuticals. Over time, businesses and environmental chemists succeeded in identifying, isolating, and cataloguing this compound because of its robust reactivity and simple three-point substitution pattern. Its growth in industry reflected serious demand from sectors needing reliable, chemically straightforward building blocks that do their job with no surprises.

Physical and Chemical Qualities

3-Chlorophenol doesn’t draw attention to itself at first glance—it stands as a white to pale yellow solid with a sharp, medicinal odor that escapes easily into the air. It floats somewhere between the simple phenols and heavier chlorinated organics when it comes to volatility and persistence. 3-Chlorophenol melts just below body temperature, and it dissolves in a limited way in water, far better in organic solvents. Its backbone supports simple transformations. The chlorine atom at the meta-position confers a resistance to direct oxidation that chemists use to their advantage. In volatile chemical processes or bench-top reactions, it demonstrates both the stubborn qualities of chlorinated aromatics and the reactivity linked with open phenolic groups.

Technical Specs and Handling Practices

In practical settings, 3-Chlorophenol tends to arrive in tightly sealed containers, designed to limit vapors and protect handlers. Chemists rely on its well-documented boiling and melting points, solubilities, and reactivity guidelines to both anticipate outcomes and avoid surprises. For labeling, standard chemical naming conventions like IUPAC rule, but synonymous trivial names still circulate among those who spent time in legacy institutions before GHS and strict regulatory harmonization. Proper storage calls for cool, dry environments with local exhaust to prevent lingering fumes—old-school chemists remember the sharp, almost nostril-clenching odor and treat it with respect. Workers who spend their days with this material also take care to factor in the modest skin and eye irritancy risks, donning chemical-resistant gloves and splash-proof eyewear long before compliance made that a rule.

Making 3-Chlorophenol: Methods and Chemistry

3-Chlorophenol does not appear spontaneously; industrial routes overwhelmingly harness monochlorination of phenol itself, utilizing chlorine gas or related reagents under tightly controlled temperatures and catalyst conditions. By adjusting mixture acidity and batch timing, manufacturers nudge the reaction toward the meta-isomer, though byproducts including 2- and 4-chlorophenol demand separation steps. Each plant has stories about managing the delicate interplay between yield and impurity profiles. These processes forged the standards that today’s chemicals meet, whether destined for further transformation or as markers in environmental analysis. Researchers explored catalytic hydrogenation, directed ortho-metalation, and even electrophilic substitution on protected phenolic intermediates, but the old process remains dominant by scale and cost.

Expanding Reactions and Creative Modifications

In synthetic chemistry, 3-Chlorophenol plays a flexible but assertive role. Its lone chlorine atom enables classic nucleophilic aromatic substitution when paired with strong bases or when reacting partners pack enough punch—opening doors to ethers, amines, and other aryl derivatives that find their way into agrochemicals and specialized polymer additives. Its phenolic OH group still reacts in esterification, etherification, and even serve as a launching point for more esoteric Suzuki or Buchwald couplings. Some of my old labmates tinkered with diazotization and related modifications, using 3-Chlorophenol as a testbed for just how far you can push traditional aromatic chemistry in the search for new drugs, dyes, and ligands.

Names Across Time

Working chemists know 3-Chlorophenol by a handful of names, often tied to their training or reference texts—m-Chlorophenol, meta-Chlorophenol, and the structurally descriptive 3-hydroxychlorobenzene. Chemical catalogues and older storage cabinets sometimes reveal custom in-house shorthand or legacy tags. No matter what it’s called, its fingerprint infrared spectra and retention times in modern chromatographs guarantee chemists can spot it from mixtures—too many environmental field studies have proven that point.

Safety, Norms, and Working Standards

Early on, the hazards of phenolic compounds faded into the background—many learned the hard way to treat these materials with respect. 3-Chlorophenol, like its cousins, presents both acute and chronic health risks, particularly by inhalation and skin contact. Modern operational protocols address this threat with fume hoods, proper PPE, spill control kits, and training that drives home what can happen when even a small spill is ignored. Regulatory bodies such as OSHA and the European Chemicals Agency have laid down rules for limits on airborne concentrations and waste disposal. Companies and universities, from urban synth-labs to rural water-testing outfits, check the air, double-bag wastes, and keep meticulous paperwork on all handling events. A generation ago, some might cut corners; today, that attitude means closed doors and lost licenses.

Where 3-Chlorophenol Finds Work

This compound’s utility stretches far. Pesticide researchers used it as a backbone to create agents that protected crops while sometimes stoking environmental debates. Pharmaceutical innovators built antibiotics and analgesics from its scaffold, drawn by the blend of chemical reactivity and biological persistence. Environmental chemists studied it as both an industrial byproduct and a marker of post-combustion waste, tracking its fate in soil and water with high-tech sensors and chromatography. Water-treatment professionals monitored its levels to protect both supply integrity and public health. In the world of dyes and resin additives, 3-Chlorophenol brings a functional group that modulates solubility and makes polymer chains more manageable for niche manufacturing needs. Not every compound sees this level of attention from such a diverse crowd—3-Chlorophenol had to earn it through a mix of chemical performance and (sometimes) regulatory scrutiny.

Pushing the Research Envelope

The questions leftover from years of 3-Chlorophenol use continue: What breaks it down fastest? Which biological systems struggle with it, and which find a way to survive? Researchers have chased answers by developing new catalysts, harnessing genetically modified bacteria, and rethinking treatment processes for industrial effluents. Some chemists look at chlorophenols as templates for “greener” chemistry, reconfiguring them to participate in less hazardous reactions or to be more easily filtered from wastewater. The field keeps evolving, spurred on by funding targeted at environmental cleanup and sustainable syntheses. Graduate students opening lab drawers cluttered with sample vials might notice 3-Chlorophenol popping up in new roles—as reference materials, as part of combinatorial chemical libraries, or as reaction partners in the latest radical chemistry advances.

Understanding Toxicity and Staying Ahead of Risks

Plenty of studies over decades reveal that 3-Chlorophenol brings real toxicity concerns. It irritates skin, eyes, and notably the respiratory tract at low concentrations. Higher doses challenge major organ systems, sometimes overwhelming detoxification processes in animals and humans. No one forgets the landmark animal studies showing liver and kidney stress or the environmental reports connecting lingering contamination to aquatic species decline. Regulators watch for soil and groundwater buildup, linking long-term exposures with developmental risks. Labs track exposure using blood and urine samples, and medical teams prepare for accidental exposures with protocols built on decades of clinical trials and emergency room experiences. People working with this material keep respect front and center—no shortcut is worth the hazard.

Where the Future Might Lead

Research communities and industry panels meet now with a new challenge—keeping necessary, effective chemicals like 3-Chlorophenol in responsible use while cutting down on the risks. Innovations in green chemistry might open alternative pathways to get the same industrial reactivity from non-chlorinated analogues. Bioremediation teams harness new microbes and cleaner energy inputs to break up the persistent footprints of past use. Regulations continue tightening, driving labs and manufacturers to adopt pollution controls, cleaner synthesis, and transparent reporting practices. In advanced materials, designers probe whether modified phenolic frameworks can replace or outperform traditional agents in electronics, plastics, and coatings. As tools for environmental monitoring grow sharper, the margin for error shrinks. 3-Chlorophenol’s long history echoes into every new debate about sustainability, safety, and the honest tension between scientific ambition and responsible stewardship.




What is 3-Chlorophenol used for?

What 3-Chlorophenol Is

3-Chlorophenol is a chemical you find in a lot more places than the name might suggest. It’s a simple phenol—think of a benzene ring, one of the most basic structures in chemistry, with a chlorine atom stuck onto its side. The “3” just tells chemists where that chlorine is attached. At first glance, it looks pretty basic, but its uses make it more important than it might appear on the surface.

Everyday and Industrial Uses

Walk down the cleaning products aisle, and chances are strong some bottles on those shelves started life with 3-Chlorophenol. Companies add it to disinfectants, antiseptics, and preservatives. It helps keep bacteria and fungi from growing in places they aren’t welcomed—think hospital cleaners, personal care products, and industrial solutions. In my own years working in a campus lab, I can’t count how many times I saw chemicals like this listed in the ingredients on bottles under the sink.

Outside the cleaning world, 3-Chlorophenol plays a role in making pharmaceuticals and pesticides. Chemists use it as a building block—they stitch it together with other chemicals to make things like herbicides, dyes, and certain medicines. It’s not usually the star ingredient, but it helps manufacturers reach the desired results during synthesis. Its ability to act as a precursor opens up a lot of possibilities for product development—from crop protection chemicals that keep fields free of weeds to agents in making certain diagnostic tests in healthcare.

Health and Environmental Concerns

Not all uses of 3-Chlorophenol come with a bright side. It packs a punch—high exposure causes irritation to skin, eyes, and lungs. The body doesn’t break it down quickly, so it can stick around longer than you’d like if it gets into groundwater or rivers. I once watched a fellow researcher handle a related compound without gloves—she ended up in the student health clinic with a nasty burn and lasting chemical sensitivity. That makes personal protective equipment—goggles, gloves, fume hoods—non-negotiable.

Runoff and improper disposal cause trouble at the community level too. Studies link phenolic compounds like this one to toxic effects in aquatic life, sometimes wiping out fish populations and hampering water quality for years. Certain manufacturing plants in regions without strong environmental oversight have polluted surrounding neighborhoods with phenols. Historically, some local communities have taken the brunt of this pollution, with water tests showing harmful levels even decades after the original spill.

Solutions and Safer Practices

Companies can’t pretend chemicals like 3-Chlorophenol don’t have downsides. It makes a difference to track inventory, train workers thoroughly, and keep strict waste protocols in place. Regular safety drills and real consequences for violating policies send the message that safety isn’t optional. At home, reading product labels and switching to less toxic alternatives where possible keeps exposures down. Some cities offer hazardous household waste days—taking the extra step to drop off old solvents and cleaners protects both people and the environment.

Research keeps pushing for replacements that do the same job with less impact. Green chemistry initiatives encourage manufacturers to rethink entire processes and swap out the toughest ingredients. Until those alternatives become mainstream, knowledge and caution play an outsized role in protecting both people and places from chemicals like 3-Chlorophenol.

Is 3-Chlorophenol hazardous to health?

Everyday Chemicals, Lasting Impact

People do not usually talk about 3-chlorophenol at the dinner table, yet it slips into the world through industries, factories, and sometimes even nearby rivers. This chemical helps in making dyes, drugs, and pesticides. It appears in cleaners and disinfectants, so it finds its way closer than you might think.

The Health Side of the Story

Most folks wonder, “How much exposure truly matters?” A whiff or touch every once in a while doesn’t always make the body shut down, but constant contact tells a different story. Short-term exposure can cause irritation—think itchy or burning skin, watery eyes, trouble breathing if fumes fill the air. Workers in places where this chemical hides in raw form risk headaches, nausea, and coughing. Just smelling that medicinal, musty odor turns most people away, but when it lingers, that’s a red flag.

What scientists worry about most is what happens over months and years. Animal studies show that too much 3-chlorophenol can throw the liver and kidneys into trouble. Some studies report the chemical changes genetic material, raising concerns over mutations and even cancer, although big agencies say solid human evidence remains scarce. The uncertainty doesn’t wipe away real risks—cancer warnings come from experimental data and how similar chemicals act in humans.

Water, Soil, and Real-World Worries

Factories using or producing this chemical can release it into water or soil by accident or through leaks. Once it gets there, 3-chlorophenol does not vanish right away. People who drink or bathe in contaminated water end up exposed through skin or by swallowing a glass of tap water. Farmers sometimes find their crops impacted when the substance moves from soil to roots. Old cleanup stories have taught entire towns just how hard it is to get rid of these pollutants.

Once in the environment, this chemical breaks down, but not fast enough. It clings to soil particles and sticks around in groundwater, winding up in places where kids play or people grow food. Tests show high levels near old waste sites or factory lagoons, and that’s where concerns run highest.

Steps for Protecting Health

No need to sit back powerless. Simple steps block much of the risk. Workers can rely on gloves, tight-fitting goggles, and special ventilation at job sites. Regular safety checks and air quality monitoring keep honest records of what floats in the air. Local water boards keep tabs on pollutants, and anyone living near old industrial zones can demand strong cleanup efforts.

Beyond factories and water pipes, the real driver shows up in policies. Strict handling rules and disposal practices keep accidental spills from ruining more communities. That requires more than just testing once a year. Whenever contamination shows up, removing polluted soil or filtering water costs money, but the trade-off comes with fewer sick children and healthier neighborhoods.

Looking Ahead

Learning about 3-chlorophenol’s hazards means putting knowledge to work. People sharing information with their communities and pressing leaders for better regulations make a difference. Trust comes from action, not empty promises. The right to clean air and clean water should never be up for debate, even in the shadow of a little-known chemical.

What safety precautions should be taken when handling 3-Chlorophenol?

Understanding the Risks Behind 3-Chlorophenol

3-Chlorophenol carries a reputation among lab workers for a quick, sharp stink and the way its toxicity sneaks up if you drop your guard. Working with this chemical, I learned quickly how easy it is to underestimate a bottle with a plain white label. The main dangers lie in its ability to irritate the skin, eyes, and, more seriously, the lungs if vapors escape. Long exposures and spills take these risks to another level, possibly even causing organ damage over time. In my own early days in the lab, I watched a small spill turn a routine session into a scramble for safety showers and eyewash stations.

Personal Protective Choices Matter

For anyone needing hands-on work with 3-Chlorophenol, clothing means more than a standard white coat. Lab experience taught me nitrile gloves hold up much longer against organic solvents than standard latex, which breaks down much faster. A face shield or at least chemical goggles stop splashes reaching your eyes. Over time, I stopped short-changing masks, switching from simple dust masks to proper respirators with organic vapor cartridges—chemical fume hoods truly prove their value here, letting air filtration do its heavy lifting.

Storage: An Ounce of Prevention

Mismanaged storage is one of the fastest ways for a chemical like this to cause trouble. I’ve seen how aging containers and poor labeling spark confusion. 3-Chlorophenol doesn’t do well under direct light or heat, so stashing it in dedicated cabinets for toxics, away from acids and bases, makes all the difference. Always choose glass or HDPE, and keep containers sealed tight—the smell alone is a warning sign if something leaks.

Cleanups: No Shortcuts

Every safety briefing stresses it, but only a live spill burns the lesson into memory. Once, I watched colleagues skip full cleanup and only circle the spot with paper towels. Hours later, headaches and watery eyes spread around the room. To avoid this, I stick with absorbent pads rated for organic chemicals, scooping up every bit for proper disposal. If any doubt exists about air quality, a portable VOC meter offers reassurance—I've borrowed one before and picked up lingering fumes where nobody expected. No matter how careful anyone tries to be, spilling is a fact of life, but half measures should never count as clean.

Handling Emergencies with Confidence

Accidents happen even to people who stay careful. Eyewash stations and showers, if kept free of clutter, mean the gap between discomfort and serious harm stays small. Quick action relies on everyone keeping first-aid materials close at hand, not tucked away in a back office. Safety data sheets belong front and center, not buried in a binder. On one occasion, quick access to documentation and nearby antidotes prevented what could have been a much worse outcome for a colleague exposed to a higher dose.

The Importance of Reliable Training and Culture

A responsible approach demands more than equipment and formal rules. Habits passed from senior staff, along with open conversations about near-misses and lessons learned, have shaped how I work today. It isn’t about just ticking boxes or running drills; it means staying alert every time and encouraging questions, no matter how basic. An environment that values speaking up over saving face can spare everyone a lot of regret.

Looking Forward

3-Chlorophenol poses real risks, but attention to gear, space, cleanup, and habits minimizes harm and anxiety. Seeing the difference between labs that invest in training and those that treat safety as an afterthought convinced me good practices provide freedom to do challenging work without needless fear. Reliable safety steps aren’t luxuries; they create the baseline for getting important research done right.

How should 3-Chlorophenol be stored?

Why Proper Storage Matters for 3-Chlorophenol

Most folks probably haven’t heard much about 3-chlorophenol unless they’ve worked in a lab or maybe dealt with chemical manufacturing or water treatment. As someone who’s handled chemicals firsthand, I can tell you that 3-chlorophenol has a reputation that deserves respect. This compound brings serious health and environmental risks if ignored. Exposure through skin contact or fumes, even in small amounts, can irritate not just your hands or lungs but can ripple out to everyone nearby. A little bit escapes, and suddenly there’s a safety officer knocking on your door, not to mention the potential for a hazardous cleanup. The key to safety always starts in how we store it.

Understanding the Hazards

3-chlorophenol doesn’t just smell sharp and pungent, it’s toxic. It’s classified as a hazardous substance, and mishandling it can mean health troubles ranging from chemical burns on skin to long-term lung issues. On top of that, spills love to sneak into drains and, eventually, into water supplies. Protecting people, property, and the wider environment starts with choosing the right storage setup.

Real Solutions in the Real World

From my own experience, too many accidents happen because someone took a shortcut with storage. A simple shelf in the corner won’t cut it. 3-chlorophenol demands secure, properly labeled containers. Glass bottles with tight seals hold up better than plastics, which sometimes react or weaken over time. Don’t trust just any container, either—chemicals like this can melt through the wrong material or corrode weak metal. What’s needed: containers made from materials proven to resist phenolic compounds, and sealed well enough so fumes can’t escape.

Look for a dedicated chemical storage area, not just a spot next to cleaning products or food. Ventilation makes a difference, too. Closed rooms trap vapors, which means anyone popping in faces a big risk of inhaling something nasty. Place storage lockers near external walls or in rooms with specialized fume hoods and proper airflow. Don’t underestimate signage, either. Bold, clear warnings prevent confusion—a coworker shouldn’t have to guess what’s inside a dusty brown bottle. Good labels show hazard class, emergency instructions, and the date received. This helps keep tabs on how long it’s been sitting around, reducing surprises from old or leaking containers.

Fires and Spills: Expecting the Unexpected

Over the years, I’ve seen how a missed step can turn a simple oversight into a nightmare. 3-chlorophenol reacts with strong oxidizers and forms flammable vapors around heat or open flames. Nobody thinks a fire will break out until it’s too late—so keep sources of ignition far from the storage zone. Sprinklers and foam extinguishers should sit close by. Steel spill trays under shelves often catch leaks before they reach the ground or drains. Training every staff member, from the new intern to the senior chemist, helps prevent the classic “I didn’t know” excuse that leads to emergencies.

Solutions Start with Small Details

Simple routines like regular inspections catch corrosion before a leak forms. Never store 3-chlorophenol alongside food, acids, or oxidizers—those combinations cook up dangerous reactions. Keep detailed logs: who used it last, what was the condition, did they notice any weird smells or discoloration. In the end, these habits save more than inventory—they protect lives and keep local communities safe. With chemicals like 3-chlorophenol, small steps add up to big results.

Is 3-Chlorophenol soluble in water?

Why Chemists and Environmental Experts Pay Attention to Solubility

Most chemicals we run into at the lab or on the job site come with a small but crucial question: do they mix with water? That question matters a lot for 3-chlorophenol. This compound often shows up in industrial processes, from making pesticides to dealing with wastewater. Once it’s out in the world, where it lands decides if it becomes a headache or just another handled chemical.

The Reality of 3-Chlorophenol in Water

3-Chlorophenol has a single chlorine atom attached to a benzene ring with a hydroxyl group. Its structure doesn't scream “highly soluble,” but it doesn’t stay dry either. At room temperature, about 28 grams of 3-chlorophenol can dissolve in a liter of water. That’s much higher than many other aromatic chemicals that carry a halogen tag. It doesn’t drift along with oil slicks; it can find its way into rivers, lakes, and even tap water under the wrong circumstances.

Importance Beyond the Surface

My background in environmental lab work tells me these numbers shape real-world decisions. Public health and soil cleanup teams both keep a careful eye on anything that dissolves readily in water, especially if the compound is toxic or persistent. Once in water, 3-chlorophenol travels. These mobility concerns mean it can sink into groundwater, ride along with drainage, and slip through soil barriers if not managed right.

The story doesn't end with just numbers or chemistry textbooks. If wastewater, for example, picks up even small amounts of 3-chlorophenol, that water brings the chemical to irrigation systems or aquifers. That pushes up the risk for crops, fish, and any person turning on a tap.

Environmental and Health Considerations

The environmental footprint of 3-chlorophenol depends on how much finds its way into water and how long it sticks around. Bacteria can, under the right conditions, break down some of it, but the process may move slowly—especially if the water is cold or short on oxygen. That lag means 3-chlorophenol can stick around long enough to do harm. Animal studies link this chemical to skin and respiratory irritation, and there’s concern about its breakdown products, some of which can be even more toxic.

Communities living near factories or landfills often worry about small leaks or spills. I’ve spoken with water treatment operators checking for phenolic compounds in daily tests. They know these numbers shape which filtration system to use and how often to check downstream wells. City planners, too, weigh these details when authorizing new industrial projects near protected wetlands or neighborhoods drawing water from shallow aquifers.

Finding Solutions at Source and Downstream

Chemical solubility guides action. Industrial managers can reduce risk by switching to closed-loop processes, so 3-chlorophenol doesn’t escape into the water stream in the first place. Water treatment plants sometimes rely on advanced filtration, like activated carbon, to catch what slips through. My experience shows that vigilance helps, but the gear only works as well as the daily attention given to monitoring and maintenance schedules.

Regulators lay down strict limits on phenolic compounds discharged into waterways. Enforcement only goes so far; many long-term solutions need cooperation from industry, cheerfully funded research into greener alternatives, and support for citizen science to track local water quality. Scientists working on detection methods for trace contamination keep improving how small spills get spotted before they grow into big threats.

The reality is that solubility in water calls for science, sensible management, and honest communication among everyone sharing the same water table.

3-Chlorophenol
3-Chlorophenol
3-Chlorophenol
Names
Preferred IUPAC name 3-Chloranylphenol
Other names m-Chlorophenol
meta-Chlorophenol
3-Hydroxychlorobenzene
3-Chlorohydroxybenzene
Pronunciation /ˌθriːˌklɔːrəˈfiːnɒl/
Identifiers
CAS Number 108-43-0
3D model (JSmol) `3DModel = "3-Chlorophenol" : {"mol":"3-Chlorophenol\nJSmol\n18\n\n C1 = CC(=CC(=C1)Cl)O\n"}
Beilstein Reference 1209221
ChEBI CHEBI:3726
ChEMBL CHEMBL14219
ChemSpider 5209
DrugBank DB02258
ECHA InfoCard 03abf958-41ac-4945-bb80-c40e18368463
EC Number 3.1.1.25
Gmelin Reference Gmelin Reference: **82806**
KEGG C01574
MeSH D021222
PubChem CID 7046
RTECS number SN6475000
UNII NSJ4LU1D5S
UN number UN2021
Properties
Chemical formula C6H5ClO
Molar mass 128.56 g/mol
Appearance Colorless to pale yellow liquid
Odor Phenolic; penetrating
Density 1.306 g/cm³
Solubility in water Moderately soluble
log P 1.95
Vapor pressure 0.47 mmHg (25°C)
Acidity (pKa) 8.39
Basicity (pKb) 15.56
Magnetic susceptibility (χ) -64.0·10⁻⁶ cm³/mol
Refractive index (nD) 1.553
Viscosity 2.38 mPa·s (20 °C)
Dipole moment 1.98 D
Thermochemistry
Std molar entropy (S⦵298) 109.8 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -73.6 kJ/mol
Std enthalpy of combustion (ΔcH⦵298) -3207.3 kJ/mol
Pharmacology
ATC code D08AE01
Hazards
Main hazards Harmful if swallowed, toxic if inhaled, causes skin and eye irritation, harmful to aquatic life.
GHS labelling GHS02, GHS05, GHS06
Pictograms GHS05,GHS06
Signal word Danger
Hazard statements H301 + H311 + H331, H315, H319, H335
Precautionary statements P280, P273, P302+P352, P305+P351+P338, P332+P313, P337+P313, P362+P364
NFPA 704 (fire diamond) 3 2 2
Flash point 79°C
Autoignition temperature 120 °C
Explosive limits 4.7–28%
Lethal dose or concentration LD50 oral rat 695 mg/kg
LD50 (median dose) LD50 (median dose) of 3-Chlorophenol: 420 mg/kg (oral, rat)
NIOSH CN8575000
PEL (Permissible) 5 ppm
REL (Recommended) 0.1 ppm
IDLH (Immediate danger) 50 ppm
Related compounds
Related compounds Phenol
2-Chlorophenol
4-Chlorophenol
2,4-Dichlorophenol
3-Bromophenol
3-Nitrophenol