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Tetrabromomethane: An In-Depth Commentary

Historical Development

Tetrabromomethane, known by many as carbon tetrabromide, carries a fascinating backstory rooted in laboratory curiosity and early synthetic chemistry. It entered the spotlight during the 19th century, as researchers sought to explore the diverse set of possible halogenated methanes. By swapping bromine for chlorine, pioneers constructed a heavier and denser version of famously dense carbon tetrachloride. Discovery, followed by industrial scale-up, aligned with periods of intense demand for dense, stable compounds in both organic synthesis and practical applications. Having spent years in university organic chemistry labs myself, tetrabromomethane’s place on the shelf was always a little different—labelled with an extra layer of caution, discussed in lectures as both a staple reagent and a material demanding careful handling.

Product Overview

Manufacturers supply tetrabromomethane as a high-purity crystalline solid or in tightly sealed bottles containing chunky white powder. Bulk purchasing supports industries seeking reliable agents for chemical transformations, notably as heavy liquid in mineral separation and advanced organic synthesis. My own experience has shown that shelf life hinges on storage: light and humidity can lead to partial decomposition and color changes. Companies premiumize products with detailed labeling, including purity metrics often topping 98 percent, and flagging strict shelf and shipping requirements. Users downstream frequently include geology labs, research centers, and some sectors in pharma where niche chemical transformations benefit from the properties carbon tetrabromide brings.

Physical and Chemical Properties

Tetrabromomethane pours out as dense, colorless to pale yellow crystalline powder, but fumes never escape careful chemists’ attention. With a molecular weight over 331 g/mol, it defines “heavy” for an organic compound. This material resists dissolving in water, instead favoring non-polar or halogenated solvents. Its melting point sits around 94°C, making transitions from solid to liquid easy enough with a simple warm water bath in the lab. Its high density (above 3.4 g/cm³) lands it as a go-to for dense solution-based mineral sorting. Bromine atoms hug the lone carbon at the center, producing a molecular geometry that stands up to many reactive conditions, short of very strong reductants or high heats.

Technical Specifications & Labeling

Reliable suppliers publish specification sheets with meticulous detail, often noting CAS number 558-13-4, purity thresholds, contaminants such as free bromine content (kept under strict limits), and moisture values. Manufacturers warn of color changes as the first sign of decomposition and always list batch-specific spectroscopic verification data. Labels emphasize secure, cool storage, away from strong light; improper conditions can trigger slow release of bromine, a definite safety concern. For anyone purchasing, every canister or bottle arrives with directions for use, emergency response, and environmental precautions reflecting domestic and international standards. From what I've seen, researchers and industrial users rely on comprehensive Safety Data Sheets to back every shipment; carelessness spells exposure risks no one wants to handle.

Preparation Method

Synthesis rests on direct halogenation, a bold yet simple chemical trick: saturated hydrocarbons bathed in liquid bromine, heated gently, and initiated through radical chain reactions. In classic lab settings, folks have used chloroform or carbon disulfide as the base, bubbling bromine through in presence of a UV lamp or chemical initiator. This method, while reliable, requires fine-tuned temperature and timing to avoid overbromination or noxious byproducts. The heavy byproduct mass complicates purification, and strict fume control keeps bromine’s volatility in check. Labs producing CBr₄ at any significant scale build exhaust systems and invest in up-to-date glassware to keep both product yield and personnel safety in balance.

Chemical Reactions & Modifications

Tetrabromomethane stands ready as a core reactant in several organic processes, especially those demanding a compact and potent source of bromine. Chemists use it for targeted alpha-heteroatom insertions, but its starring role lands in the Appel reaction—where it acts as a halogenation agent to convert alcohols into alkyl bromides. With triphenylphosphine present, it strips water from primary and secondary alcohols with ruthless efficiency. As a chemical modifier, CBr₄ reacts with strong nucleophiles to create a host of brominated organic intermediates used in agrochemical and pharmaceutical synthesis. In my own experience, the tell-tale cloud of white fumes after an Appel reaction using tetrabromomethane always called for patience and ventilation.

Synonyms & Product Names

Tetrabromomethane appears under a long list of synonyms in textbooks and supply catalogs. Carbon tetrabromide is most common, flanked by CBr₄ in shorthand. Old literature might mention bromomethane, though that misleads due to confusion with methyl bromide. Overseas suppliers sometimes use “carbonium tetrabromide” or list the compound by its registry numbers, but frontline users lean into recognizable common names. Supply houses selling high-purity versions market under distinct brands or as “Reagent Grade Carbon Tetrabromide.” Those hunting for a supplier often crosscheck these names to avoid picking the wrong halogenated methanes.

Safety & Operational Standards

Daily users uphold a strict regimen of safety procedures surrounding tetrabromomethane, reflecting its toxicity, reactivity, and environmental risks. Direct contact with skin or inhalation of dust can irritate or sensitize; chronic exposure builds up health effects that only manifest months later. Standard laboratory PPE—gloves, goggles, full ventilation—form the minimum line of defense. Industry guidelines from OSHA and similar agencies insist on secure, ventilated storage and seamless chemical waste collection. I’ve witnessed firsthand how strict adherence to these standards in an academic lab setting can mean the difference between an uneventful synthesis and an incident requiring full evacuation and medical attention. Even small-scale academic work with CBr₄ nets frequent spot-checks for leaks, warning sign inspections, and regular training refreshers for all involved.

Application Area

Demand for tetrabromomethane stretches across research, mining, and advanced manufacturing. Geologists value CBr₄’s density, suspending mineral fragments in heavy solutions to quickly sort ore samples. Synthetic chemists reaching for specific alkyl bromides rely on its efficiency in laboratory transformations, while electronics blending and plastics compounding use this compound for specialty polymer modifications—though modern demand shrunk compared to its peak in the 20th century, as safety and environmental legislation became stricter. In my experience as a research chemist, instructions for using CBr₄ usually came with cautionary tales: treat it as a tool with both sharp edges and keen utility.

Research & Development

Recent research has explored alternatives to tetrabromomethane in synthetic chemistry, aiming for similar reactivity with improved safety profiles. The search for greener, more sustainable halogenation agents comes from both regulator pressure and practical demand for safer labs. Studies continue to confirm CBr₄’s unique reactivity with certain substrates, though researchers constantly push new variants and process adjustments to minimize hazardous byproduct formation. Intellectual property filings and patents hint at gradual shifts—using milder conditions, closed vessels, or in situ generation of reactive bromine analogues. Collaboration between academia and industry builds on centuries of accumulated experience, digging for solutions that keep synthesis powerful without the environmental baggage older reagents bring.

Toxicity Research

Scientists have tracked the health risks posed by tetrabromomethane for decades. Animal studies show it affects central nervous systems, kidneys, and liver with acute and chronic exposure, confirming what industrial doctors suspected from early accidents. As someone who saw graduate students recover from mild exposure, I know the importance of medical response and regular monitoring. The chemical’s persistence in the environment, combined with slow release of elemental bromine or decomposition to toxic byproducts, keeps CBr₄ off the “routine” list in many labs. Toxicology research underpins regulatory restrictions and ongoing calls for improved disposal protocols, stricter lab training, and substitution where possible.

Future Prospects

Governments and manufacturers look for replacements, and research into new heavy liquids and safer alternatives takes priority. Environmental regulations drive steady decline in CBr₄’s use outside high-value applications. Future trends point towards reagents offering similar reactivity for key organic transformations with less risk to human health and ecosystems. Companies experiment with closed-loop synthesis, waste reclamation, and new protocols, betting on technology to deliver safety and utility hand in hand. Knowing the sharp edges of tetrabromomethane’s chemical power—and the costs of mishandling it—pushes industry, lawmakers, and educators to plan ahead, keeping science and society in careful balance.




What is Tetrabromomethane used for?

From Heavy Liquid to Lab Essential

Tetrabromomethane doesn’t show up in most headlines. It looks pretty basic on paper—a colorless, heavy liquid. In the real world, though, this chemical ends up in labs, factories, even in geology classrooms. Most folks know it by its other name, carbon tetrabromide, or just CBr4. The stuff can trick people with how dense it feels, thanks to all that bromine packed in a single molecule. Toss a rock or a sample of ore into a bottle of this liquid, and even experienced geologists pause to rethink what floats and what sinks.

The Science Class Connection

I remember seeing carbon tetrabromide back in my university days. Geology labs would fill tanks with the dense liquid to separate minerals. Instead of picking through grit by hand, students would drop a blended sample into the tank. The denser pieces, like zinc or lead ore, sunk right away, making sorting quicker and more accurate. This method, called heavy liquid separation, saved a lot of headaches. Places still use it, especially for academic experiments or small-scale mining research. Anyone working with valuable minerals appreciates how much time and energy this shortcut saves.

Fire Safety Wasn’t Always a Given

Decades ago, people poured carbon tetrabromide in fire extinguishers. It knocks down flames fast, especially electrical fires. Older generations remember the glass-bulb fire grenades filled with this stuff hanging in industrial buildings or workshops. In the past, folks didn’t worry as much about environmental fallout or health hazards. Now, with what’s known about brominated chemicals, the cost seems higher than people first realized. The chemical breaks down into toxic fumes if heated or burned. Most places dropped it from fire safety gear when researchers raised alarms about how those fumes affect both people and the planet.

Modern Chemistry Puts It to Work

Take a trip into organic chemistry labs, and carbon tetrabromide pops up in a different role. Chemists rely on it to add bromine atoms to other molecules. It’s especially handy in the Appel reaction, which turns cheap, common alcohols into more valuable alkyl bromides. These reactions keep drug manufacturers busy since the resulting products serve as building blocks for more complex molecules—some ending up in medicine, others in pesticides or advanced materials. Reliable sources, like peer-reviewed chemistry journals and the United States National Library of Medicine, document these applications.

The Not-So-Simple Side

Digging deeper, safety keeps coming up. Tetrabromomethane can wreak havoc on health, especially if people breathe in fumes or spill it on bare skin. Long exposure may damage organs or affect the nervous system. Today, government agencies demand strict handling precautions. Lab workers lobby for better ventilation and protective gear. Safe disposal means following hazardous waste rules, not just pouring it down the drain.

Looking Beyond Old Habits

The industry can’t rely on this chemical for everything as it did in the past. Cleaner alternatives for heavy liquid separation get better every year. Water-based options, though pricier, pose fewer health risks. Chemists invent more eco-friendly reagents for bromination, which puts some pressure on old standbys like carbon tetrabromide. Standing by the health and safety credentials, experts look for ways to replace risky chemicals altogether.

Pushing for Better Practices

Anyone responsible for science education, industrial safety, or environmental clean-up has a stake in this conversation. Trustworthy information, shared clearly and checked by experts, guides good decision-making. The conversation about tetrabromomethane shows what happens when industry, science, and public health come together to weigh risks, explore new technology, and balance cost against well-being.

Is Tetrabromomethane hazardous to health?

The Reality Behind a Common Industrial Chemical

Bottles of tetrabromomethane line shelves in chemistry labs around the world. Its reputation mostly leans on its job as a flame retardant, a cleaning agent, and sometimes as a solvent. Some folks may know it from handling heavy liquids for mineral separation back in science class. Millions never see it, but the truth of its impact on people’s health deserves a closer look.

Health Hazards That Hide in Plain Sight

I once spent a summer as a lab tech and learned pretty early that not all “routine” chemicals get equal respect. Tetrabromomethane gives off fumes that linger, with a heavy, sweet smell. That smell means danger. The body reacts quickly—dizziness, headache, and nausea come on fast when ventilation slips. Not much air, no protection, and you find out just how fast a chemical can put health at risk.

The numbers back up those dizzy spells. Even short-term exposure leads to central nervous system symptoms—confusion or fainting aren’t rare when someone mishandles this stuff. It heads straight to the brain, and higher doses do worse damage. Panicked visits to emergency rooms reinforce what workers and regulators warn about: tetrabromomethane exposure isn’t just uncomfortable, it’s a real threat.

Long-Term Risks Lurk Beneath the Surface

Take a look at chronic exposure and things get more serious. Studies over the past decade suggest that extended contact can hit the liver and kidneys especially hard. Animal research led scientists to point fingers at this chemical for liver enlargement, kidney problems, and worse. There’s even evidence linking long-term tetrabromomethane exposure to reduced fertility and birth defects in lab animals. The EPA and the European Chemicals Agency recognize these risks, warning industries to use it carefully and in strict limits.

Real-World Impact Beyond the Lab

Some of the people hurt most by hazardous chemicals don’t wear white coats, but coveralls. Factory workers get the brunt, along with waste handlers and cleaning crews. Few workers know the full risks, especially in countries where regulations stay weak. Leaks and spills rarely get reported, and long-term health effects roll out over years. Even regular folks living near some factories might inhale low levels that add up over time, though current science suggests outdoor exposure is less of a concern.

What Helps Keep People Safe

There’s nothing flashy about good ventilation and gloves. Experience in any lab or plant shows that simple steps cut the risks dramatically. Tight storage, air extraction systems that actually work, and real-time gas detection keep the workplace safe. Training goes a long way—teaching people what to look for, what to do if they spill, and how to leave no one in the dark if disaster strikes. Enforcement matters just as much. Companies that flout the law put lives at risk. Governments can raise fines and even shut places down until they follow safety codes.

Better substitutes slowly edge onto the market, though change takes time. As more industries switch out brominated chemicals, the risks to both people and the planet shrink. Until then, honesty about the harms, proper protection, and collective oversight do the job of saving lives.

What is the chemical formula of Tetrabromomethane?

Looking Closer at Tetrabromomethane

Tetrabromomethane sounds like a mouthful, and its formula—CBr4—doesn’t roll off the tongue any easier. Still, this compound brings something more important than pronunciation to the table. As someone who spent time studying organic chemistry, the structure of molecules like CBr4 sticks with you long after the tests end. The name tells you what you're dealing with: one carbon atom, surrounded by four bromine atoms. Pretty straightforward, but the real story is in how it’s made, how it behaves, and why it shows up outside the classroom.

This Formula Packs a Punch

Anyone handling brominated compounds learns quickly that they aren't just bits of trivia for chemists. Tetrabromomethane has heft, both literally and in terms of chemical use. The molecular weight soars above that of its more famous cousin, carbon tetrachloride (CCl4), clocking in at about 331.63 grams per mole. That’s mostly the bromine talking—bromine atoms aren't lightweights. Tetrabromomethane’s high density (about 3.42 g/cm³ at room temperature) turns it into a handy tool if you need to separate minerals or test for halides in a mixture. Not a day-to-day ordeal for most people, but pretty essential in a research or mining setup.

Speaking from a student’s perspective, it really helped me remember the logic of chemical nomenclature. “Tetra” means four, “bromo” points to bromine, and “methane” shows the single carbon core. Teachers love to drill this home because it offers a roadmap for naming almost any organic molecule. It’s not about memorization, but about seeing the logic and pattern.

Tetrabromomethane and Health Concerns

Most people outside a lab probably don’t feel the direct impact of CBr4, but that doesn’t mean ignoring its risks. Brominated chemicals in general can cause health concerns. Some data links them to liver and kidney damage if exposure levels climb, and I know from safety training that even “just a little exposure” is a dangerous game. Inhalation carries particular risk, making proper ventilation and gloves an absolute must.

Combined with its persistence in the environment, CBr4 has made its way onto restricted lists in several countries. I learned early on that careless disposal sends these molecules into water sources, where they stick around. Awareness around responsible handling isn’t just a bureaucratic box to check—it’s a duty to anyone working nearby and everyone downstream.

Industry Uses and Safer Paths Forward

Industries once leaned on tetrabromomethane as a flame retardant and as a component in certain chemical syntheses because of its stability and heavy molecular weight. Times change, and so do rules. Now, alternatives step in more often, mainly because manufacturers and governments take chemical safety seriously.

I’ve seen green chemistry grow from an academic idea to an industry standard. Engineers and researchers look for ways to reduce or replace hazardous chemicals, swapping them out for less threatening options wherever possible. It’s not always easy, or cheap, but the long-term payoff supports safety and environmental health.

Building Trust Through Science

Understanding simple facts—like the formula CBr4 for tetrabromomethane—doesn’t just answer test questions. It’s a reminder that chemistry sits in the real world, shaping how we work, what we build, and how safe we all stay. A single formula, learned well, turns out to hold a lot more weight than it seems.

How should Tetrabromomethane be stored?

Storage Isn’t Just About Putting a Chemical on a Shelf

Tetrabromomethane stands out in a room of chemicals, mostly because it can pack a punch if handled carelessly. Anyone with hands-on experience in a lab learns to treat this compound with plenty of respect. Take it from someone who’s seen corners cut, safety slips up fast if you don’t pay attention to basics. The stuff doesn’t explode on you, but its fumes, leaks, and fire risks can create a mess nobody wants to clean up. So, keeping it safe, stable, and away from curious hands takes real planning—not just a locked cabinet.

What’s at Stake?

You can drink coffee next to most office supplies, but Tetrabromomethane brings a different vibe. Exposure messes with the nervous system and can irritate your lungs. Breathing the vapors can leave you with headaches or worse. Spills mean danger for both people and the environment, since it’s not going to break down easily. If you’ve ever seen regulators walk through a facility with their checklists, you know they’re looking for good practices. Mistakes lead to fines, lost jobs, or emergency room visits.

A Real-World Approach to Storing Tetrabromomethane

Let’s get practical. Most bottles and drums stay safest in a cool room, away from sunlight and heat sources. A climate-controlled space prevents the compound from breaking down over time or producing fumes. Keep it dry—moisture can cause corrosion or equipment damage, and wet floors turn a minor spill into a slip hazard or fire risk.

Ventilation deserves serious attention. Closed airlocks or small storage closets become traps for vapor, especially if there’s a leak. Good airflow—whether from local exhaust fans or a properly-designed fume hood—lets workers breathe easier and reduces the threat of long-term exposure. When investing in upgrades, select storage cabinets with chemical-resistant surfaces and secure locking mechanisms. The extra money spent on rated cabinets pays off if you face a fire or accidental knock-over.

Label Everything—Don’t Assume People Know

Those bold, clear hazard stickers shouldn’t disappear with the first wipe-down. People rotate through teams, and not everyone in a building grew up handling hazardous materials. Labels reduce confusion and save time in an emergency. If you’ve ever seen someone mix up containers or rush through inventory checks, you’ll appreciate how a properly tagged bottle cuts down on mistakes.

Keep Incompatible Materials Apart

Don’t store just anything next to Tetrabromomethane. Acids, bases, and strong oxidizers should stay in a different zone. Accidental mixing can trigger reactions that spoil more than your lunch break. Chemical incompatibility isn’t some hypothetical worry—a tipped shelf or inattentive shift can cause real damage. Regular training and checklists help teams spot risky combinations before trouble starts.

Emergency Planning Isn’t Just for Compliance

I’ve seen the difference between companies that rehearse spill response and those that wing it during a crisis. Eye-wash stations, emergency showers, and spill containment kits should sit close to where the chemical lives. Emergency contacts and procedures need display in plain sight, with a fresh copy for every shift. Response drills matter. Teaching crews how to handle problems calmly can turn a scary moment into a minor inconvenience.

Culture Makes the Biggest Difference

Storing Tetrabromomethane correctly boils down to attitude as much as equipment. If safety culture takes a back seat, even the fanciest cabinets won’t help. Open conversation, good records, and a willingness to learn from close calls keep things running smooth—and everyone goes home healthy.

What are the physical properties of Tetrabromomethane?

Tetrabromomethane, Up Close

Step up to the workbench and grab a bottle marked CBr4. Tetrabromomethane — heavy, with a formula built from one carbon atom holding on to four bromine companions. Each bromine lugs a lot of weight, giving the whole molecule a dense character. Try lifting a container of the crystalline solid. Once, at the university storeroom, I clocked just how unexpectedly heavy it felt: a scoop of what looks like sugar, but nearly five times denser than water. That’s not your average household compound.

Density That Packs a Punch

At room temperature, Tetrabromomethane forms colorless to white crystals. The density hits about 3.4 grams per cubic centimeter. To put it in perspective, that’s lighter than lead but miles heavier than most organic solids. Spill some into a beaker of water, and it sinks straight to the bottom, dragging stray bits of glass or sand down with it if you’re messy. This density has made it a favorite in mineral separation and heavy liquid experiments.

Melting and Boiling Points Fit for Lab Use

Its melting point sits just above body temperature, around 95 degrees Celsius. I’ve watched it go from solid to liquid in a flask just by twisting the heat dial on the hotplate. Some folks use it as a calibration marker in melting point apparatus, since it transitions so crisply. Push the heat further, and Tetrabromomethane boils by the time you hit 189 degrees Celsius. These numbers matter if you’re storing or transporting it — the stuff needs careful handling in a warm warehouse.

Solubility That Draws a Line

Put Tetrabromomethane in water, and it all but ignores it. The molecules clump together, too heavy and nonpolar to mix. Not so in organic solvents. In my first year lab, we’d dissolve it in chloroform and benzene in seconds — proof that like dissolves like. This makes Tetrabromomethane flexible in synthesis. Chemists lean on these solubility quirks to extract or purify materials, keeping workflows tidy and separation simple.

Appearance and Odor Speak Volumes

Take a close look: clear, shining crystals, with a whiff that rides chemical but not harsh. It doesn’t grab your nose like ammonia or diethyl ether. That low volatility helps — it doesn’t leap into your airspace at room temp, so you can work with it a bit longer, as long as nobody forgets to crack a window.

Stability, Reactivity, and Handling

Tetrabromomethane stashes its energy tight. It doesn't burst into flames or decompose fast under normal conditions, but heat it enough and you’ll smell traces of bromine splitting off, especially under light or in the presence of strong reducing agents. It’s best to use a fume hood, gloves, and common sense. Safety sheets push for storage in amber bottles, away from sunlight. I’ve seen what can happen if someone leaves the cap off: crystals darken and smell sharper, which sends all the right warning signals.

Why These Traits Stick Out

Every one of these physical quirks — from its weight to the stubbornness with water — drives choices in geology, chemistry, and beyond. When I taught introductory mineralogy, I’d pour a tablespoon of this heavy liquid into a dish to sort out tiny stones; nothing brings science to life like watching dense grains hover and sink. Handling Tetrabromomethane calls for practical safety, clear labeling, and respect for both its uses and its risks. That’s how knowledge lasts in the lab and on the job.

Tetrabromomethane
Tetrabromomethane
Names
Preferred IUPAC name Tetrabromomethane
Other names Carbon tetrabromide
Tetrabromocarbon
Bromocarb
Tetra-bromo-methane
Pronunciation /ˌtɛtrəˌbrəʊməˈmiːθeɪn/
Identifiers
CAS Number 558-13-4
Beilstein Reference 1209225
ChEBI CHEBI:47498
ChEMBL CHEMBL25416
ChemSpider 5468
DrugBank DB02933
ECHA InfoCard 100.970.011
EC Number 200-955-8
Gmelin Reference 1171
KEGG C10262
MeSH D002073
PubChem CID 11207
RTECS number PA0350000
UNII YOW8V9698H
UN number UN2516
Properties
Chemical formula CBr4
Molar mass 331.627 g/mol
Appearance White crystalline solid
Odor Odorless
Density 3.42 g/cm³
Solubility in water 0.33 g/100 mL (25 °C)
log P 1.94
Vapor pressure 0.01 mmHg (20°C)
Acidity (pKa) -0.24
Magnetic susceptibility (χ) -68.0·10⁻⁶ cm³/mol
Refractive index (nD) 1.602
Viscosity 2.22 mPa·s (20 °C)
Dipole moment 0 D
Thermochemistry
Std molar entropy (S⦵298) 146.6 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -13.4 kJ/mol
Std enthalpy of combustion (ΔcH⦵298) -707.8 kJ mol⁻¹
Pharmacology
ATC code V09AA03
Hazards
GHS labelling GHS02, GHS07, GHS09
Pictograms GHS06,GHS08,GHS09
Signal word Danger
Hazard statements H302, H315, H319, H335
Precautionary statements P210, P261, P271, P280, P301+P312, P304+P340, P305+P351+P338, P312, P337+P313, P403+P233, P501
Autoignition temperature 185°C
Lethal dose or concentration Lethal dose or concentration (Tetrabromomethane): "LD50 oral rat 2500 mg/kg; LC50 inhalation rat 253 mg/m3/4h; LD50 dermal rabbit >10 g/kg
LD50 (median dose) 4300 mg/kg (rat, oral)
NIOSH WA8575000
PEL (Permissible) PEL (Permissible Exposure Limit) of Tetrabromomethane: "0.1 ppm (1 mg/m3) as an 8-hour TWA (OSHA)
REL (Recommended) 200 mg/m³
IDLH (Immediate danger) 500 ppm
Related compounds
Related compounds Carbon tetrachloride
Methane
Chloroform
Bromoform
Iodoform