Bromohexane: A Grounded Look at a Unique Chemical Compound
Historical Development
The story of bromohexane traces back to early 20th-century organic chemistry. Chemists, searching for better ways to manipulate hydrocarbons, started using halogenation. Bromohexane, produced by adding bromine to n-hexane, came from these early halogen experiments. Laboratories didn’t have advanced safety gear, so early work involved a fair amount of risk. Researchers soon realized bromohexane’s value as a handy alkylating agent, which meant more labs began exploring and recording its reactivity. By the time organobromides grew popular in the 1950s and 1960s, bromohexane stood out because of its 6-carbon backbone, giving it versatility for further modification. With better distillation techniques arriving in the latter half of the century, chemists could make purer batches, paving the way for research into its applications in pharmaceuticals, agrochemicals, and even materials science.
Product Overview
Bromohexane’s structure — a straight six-carbon chain with a bromine atom at one end — gives it interesting properties. It fits in with other alkyl halides, but it stands out for its balance of reactivity and manageability. It’s not the most reactive bromoalkane, which means chemists can handle it with care, without the immediate risk that comes with smaller, more volatile brominated hydrocarbons. Professionals in synthesis, research, and manufacturing reach for bromohexane when they need to insert a six-carbon chain. In the real world, it shows up as a colorless liquid, giving off an odor that reminds most people in research of solvents or cleaning agents from campus days.
Physical & Chemical Properties
Bromohexane has a formula of C6H13Br and its molar mass clocks in right at 165.08 g/mol. At room temperature, it stays liquid, with a boiling point just above 155°C and a melting point a smidge below -65°C. It doesn’t mix well with water; hydrophobicity keeps it floating or settling at the surface. The compound sits heavier than water, and its vapor is denser than air, so those working with it must ventilate properly. On the chemical side, the carbon-bromine bond gives bromohexane its reputation: the bromine atom works as a good leaving group, which lets all sorts of nucleophiles attack the carbon chain. As someone who’s handled dozens of bromoalkanes, I can say bromohexane’s reactivity is both a blessing and a challenge in the lab. It doesn’t spontaneously combust or decompose unless seriously mishandled, but carelessness leads to unwanted side reactions.
Technical Specifications & Labeling
Manufacturers selling bromohexane for research or industry provide it in amber glass bottles, since it can slowly break down if exposed to too much light. Labels need to include its chemical name, formula, sometimes the CAS number (usually 111-25-1), purity (usually 98% or higher for demanding applications), and any stabilizers used. Labs keep detailed safety data sheets on hand, listing hazards like skin and respiratory irritation, and suppliers include instructions for proper storage and disposal. Shipping has to comply with regional regulations since organobromides meet criteria for hazardous materials in many places. In my experience, technicians double-check bottle seals and records before approving use, not only to track inventory but to minimize chemical exposure.
Preparation Method
The classic route to bromohexane starts with n-hexanol, a common alcohol that’s easy to source. Adding phosphorus tribromide (PBr3) or hydrobromic acid (HBr) converts the alcohol into the bromide. The process, run in a fume hood with cooling, generates bromohexane and side products such as water or phosphorous acids. Modern green chemistry labs lean toward methods that avoid mercury, minimize waste, and favor reagents that can be recycled. For those on a budget, sodium bromide and sulfuric acid give an alternative, and even undergraduate students can safely try this with supervision. From lab to pilot scale, quality checks prevent contamination by unreacted alcohols, water, or leftover acid fumes. Purification involves careful distillation, and purity levels directly affect whether the product goes into research, scale-up, or commercial production.
Chemical Reactions & Modifications
Bromohexane plays a key role in the world of organic synthesis. Its most famous trick: acting as a sturdy alkylating agent. The bromine atom can leave, making way for many different groups to latch on where it used to be. Bromohexane enters SN2 or SN1 substitution reactions, depending on the context, and its six carbons offer a useful building block for longer molecules. In the pharmaceutical sector, I’ve seen bromohexane used for introducing functional diversity. Reacting bromohexane with an amine gives a straight-chain amine; swapping with a thio group lets chemists create thioethers. The nature of the hexyl group lets researchers tweak solubility, hydrophobicity, and chemical stability of different compounds. Those in polymer chemistry use bromohexane to modify backbones or side chains efficiently. In my own experience, success often hinges on reaction temperature, mixing rates, and the cleanliness of the starting reagents — stray water or leftover acid can turn success into a frustrating day cleaning up messes and troubleshooting yields.
Synonyms & Product Names
Chemists rarely stick to one name for long. Bromohexane shows up on shelves and in literature as 1-bromohexane, hexyl bromide, or even n-hexyl bromide. These synonyms all point to the same straight-chain compound, each labeling style preferred depending on the audience. Academic settings stick with “1-bromohexane” for clarity, especially for students trying to match their synthesis work to published research. “Hexyl bromide” finds favor in older technical manuals and some trade catalogs. Suppliers may use product codes, but no matter how it’s marketed, quality beats packaging when researchers or manufacturers are choosing a source.
Safety & Operational Standards
Working with bromohexane takes respect and preparation. Its vapor can irritate the eyes, lungs, and skin, and accidental spills on unprotected skin may cause redness or even mild burns over time. Proper handling includes nitrile gloves, safety glasses, and fume hoods to keep vapor concentrations low. I’ve worked labs where staff ignored these rules, only to regret it after getting drowsy or developing a persistent cough. Guidelines from organizations like OSHA and the European Chemicals Agency define exposure limits and emergency procedures. Storage demands sealed bottles in cool, dry places, away from sources of ignition or reactive metals. Waste handling involves collecting all washings for disposal by licensed companies, since standard drain disposal risks contamination and regulatory fines. new staff or students should always work under supervision for the first few runs and double-check all procedures before logging the work as complete.
Application Area
Bromohexane appears in surprising places. In research and development, chemists use it to build custom molecules for drugs, dyes, and agrochemicals. For pharmaceutical needs, it often serves as a starting block in the synthesis of anesthetics and antiseptics. In crop science, its carbon chain turns up in herbicide intermediates or as a precursor to compounds affecting plant metabolism. Materials scientists look at bromohexane when modifying synthetic polymers and resins, using it to introduce hexyl groups for improving flexibility or solubility. I’ve seen bromohexane’s use extend to flavor and fragrance design, though only after strict purification to keep residues below strict regulatory limits. Electronics researchers modify surfaces or prepare certain liquid crystals using alkyl bromides like bromohexane. Each application brings its own purity demands and safety requirements, shaping what suppliers provide to industry and research clients.
Research & Development
Current research circles around greener methods of production, better handling, and novel applications. Scientists study alternatives to hazardous reagents, like swapping phosphorus tribromide for less toxic catalysts or more sustainable feedstocks. Research teams look at using flow chemistry techniques to reduce waste, improve yields, and scale up processes safely. In the world of drug and polymer discovery, chemists test whether longer alkyl chains like those in bromohexane deliver better biological activity or physical performance than shorter analogues. At academic conferences, presenters share data about bromohexane’s role in molecular scaffolding, custom surfactants, and smart materials that respond to light or heat. Workforce trends push for automation and better robotics to limit direct exposure during hazardous steps. New labeling technology, including QR codes on bottles, supports real-time inventory and document access, helping staff manage compliance and reduce errors.
Toxicity Research
Bromohexane does not belong on the most toxic lists, but it isn’t harmless either. Short-term exposure at high concentrations can cause narcosis, dizziness, and respiratory discomfort. Toxicologists look at how the liver metabolizes bromohexane, often finding its breakdown products aren’t as hazardous as some other organohalogens, but still demand careful tracking. Animal studies suggest repeated skin contact can lead to mild dermatitis, and inhalation over several weeks may cause liver enzyme changes. In real-world workplaces, monitoring air and surface levels remains important particularly in small labs or industrial settings with less advanced ventilation. Accidental ingestion, which almost never happens in modern labs, would call for emergency care. Most seasoned chemists keep up with safety data and emerging research through journals or internal safety bulletins, since new findings can shift best practices. On the regulatory side, agencies keep reviewing limits to reflect updated scientific understanding and practical exposure risks.
Future Prospects
The outlook for bromohexane hinges on how well industry and research adapt to greener chemistry and stricter safety rules. Regulations grow tighter every year, steering production toward cleaner, more traceable supply chains. Interest in bio-based feedstocks could drive demand for new synthesis pathways that avoid fossil fuels. Research teams working on drug delivery, nanomaterials, and advanced polymers keep exploring the unique effects a six-carbon, bromine-capped chain brings to their projects. Cutting-edge work with flow reactors and automated synthesis might push bromohexane into more specialty roles where precision and efficiency matter most, leaving bulk commodity uses to fade as alternatives emerge. My own experience working with evolving safety standards shows how staff training, equipment investments, and better information sharing turn once-risky chemicals like bromohexane into well-managed tools for new discoveries. Teams who keep pushing for smarter practices stay better prepared for whatever changes come next in the chemical world.
Understanding Bromohexane in Everyday Chemistry
Bromohexane shows up in chemical labs more than most folks might notice. If you ever walked through a research facility, bottles marked “hexyl bromide” often sit on shelves tucked away, ready to start the next reaction. Bromohexane really means a six-carbon chain with a bromine stuck at the end—a simple swap, but one that gives it some interesting punch. Ask any organic chemist, and they’ll point out that this stuff helps build molecules that go well beyond textbooks.
Real Workhorse in Synthesis
In pharmaceuticals, everything starts with building blocks. Bromohexane steps up as one of those—particularly when a chemist wants to tack on a hexyl group (that’s just six carbons in a row) during a reaction. Alkyl bromides like bromohexane react easily with other chemicals. They “plug in” to frameworks for new drugs, turning simple molecules into ones that might end up as antiviral medicines or other treatments. The more you study organic chemistry, the more you see simple halides nudging the science forward.
Back in university labs, we’d use bromohexane to teach students about nucleophilic substitution. Put it next to a strong nucleophile, and the bromine pops off, replaced by whatever’s eager to bond. Watching that shift in a flask gave a real sense of why organic chemistry matters. Reactions like these don’t just stay in the classroom—they roll out into real-world manufacturing.
Industry Applications That Keep Things Moving
Beyond textbooks, bromohexane’s value runs deep in manufacturing. Companies crafting flavors or fragrances can use it as a starting material to build aroma chemicals. Paints, coatings, and plastics all use intermediates based off bromohexane structures. I once visited a specialty chemical plant where a simple halide like this multiplied into a dozen end products, each with a different scent, texture, or property. It’s rare to see the same compound feed so many branches of the chemical industry.
Even electronics rely on similar building blocks. Some flame retardants and specialized lubricants use halogenated chains, and bromohexane fits the bill before modifications add further safety or durability. Though not every device in your pocket or on your desk connects back to bromohexane, a surprising number of components owe their early stages to chemicals in this family.
The Safety Question and Its Solutions
Bromohexane doesn’t just come with opportunity. There’s bite to handling any alkyl bromide. Skin contact causes irritation, and breathing in vapors never helps anyone’s health. My own lab days included thick gloves and good ventilation, following every recorded protocol. Data from organizations like OSHA and the CDC supports what every chemist knows—prolonged exposure harms health. Companies and universities invest in training, fume hoods, and protective equipment. You can’t cut corners here.
Tracking sourcing and disposal also matters. Responsible producers use closed systems to stop accidental releases. Many also recycle leftover chemicals when possible. It’s good practice and makes sense for companies under increasing pressure to tighten compliance. Modern labs also swap out more hazardous reagents when safer options exist, a trend that benefits everyone downstream.
Looking Forward
Bromohexane remains a quiet engine behind plenty of progress. It fits smoothly into scientific advances, industrial production, and educational experiments, while responsible handling and substitution policies help protect both workers and the wider environment. Every bottle carries a story linking curiosity to real-world problem-solving.
Real Concerns with Bromohexane in the Lab and Beyond
Bromohexane might not grab headlines, but anyone who’s handled solvents or specialty chemicals in a lab knows it deserves respect. This compound shows up in research and industrial processes, often as a starting material for organic syntheses. I’ve worked in labs where safety sheets for chemicals like bromohexane stack up tall; the technical data always looks straightforward, but the real-world hazards can run deeper.
Health Hazards: What the Evidence Tells Us
Working with bromohexane means facing several health risks. Exposure can irritate the skin, eyes, nose, and throat, sometimes just from vapor contact. Research points to this chemical being harmful if inhaled, swallowed, or if it comes into contact with skin. Headaches, dizziness, and nausea are pretty common when proper ventilation gets neglected. Chronic exposure risks include damage to the liver, kidneys, or nervous system, especially if someone ignores basic protective measures like gloves and fume hoods.
The safety data sheets put this substance in the “harmful” and even “toxic” category depending on the context. Dermal absorption happens easily because of bromohexane’s oily nature. On lab benches, quick reactions and carelessness often lead to spills, which means a real threat of exposure. Personal experience has taught me that symptoms don’t always appear right away; a headache might creep in later, long after a short fume exposure.
Environmental Impact: Beyond Human Health
Dumping bromohexane down the drain or tossing it in the garbage brings its own set of problems. These halogenated solvents hurt aquatic life and stick around in soil or water longer than many hope. Studies show that chemicals in this family resist breaking down, leading to worries about bioaccumulation and contamination. This makes simple disposal an ongoing problem even for facilities with advanced waste management systems.
Managing the Risks: Safe Handling and Alternative Choices
Getting ahead of bromohexane hazards isn’t rocket science. A few basic habits work wonders: wear chemical-resistant gloves, keep labs well ventilated, and use goggles every time. People sometimes forget that fumes can stay in the air long after use, making air monitoring and exhaust fans critical even for quick experiments.
Training and clear labeling do more than check off items on a safety list. They help everyone remember what’s at stake. In the labs where I’ve worked, formal walkthroughs, spill drills, and easy access to safety showers made a huge difference. No one likes to admit mistakes, but quick reporting and honest reviews of incidents make sure small errors don’t grow into disasters.
Research into greener alternatives keeps moving, though not fast enough for every process. Where possible, replacing bromohexane with less toxic substances adds protection for both workers and environments. Industry needs also drive this shift, especially as regulations tighten and disposal gets more expensive.
The Value of Vigilance and Care
Bromohexane’s hazards don’t just matter to scientists or factory workers. Anyone near a spill or handling its waste faces risks. Staying aware, choosing safer chemicals, and following thoughtful safety routines means protecting more than just the bottom line; it means keeping people and environments healthy for the long haul.
Getting to Know Bromohexane
Bromohexane sounds like a mouthful, but break it down and you’ll spot the “hexane” — that’s a straight chain of six carbons. The “bromo” part? That just means one of the hydrogens has been swapped out for a bromine atom. Put it together, you get C6H13Br.
Putting the Formula to Work
Having spent a few years mixing up reagents at the lab bench, I’ve found that a clear grasp of chemical formulas saves more headaches than the most careful safety goggles. C6H13Br gives you a reusable shortcut: six carbons, thirteen hydrogens, and one bromine. It may not mean much on paper, but in a bottle, it brings both value and risk.
Bromohexane can act as an alkylating agent. In organic synthesis, it’s used to kick-start all kinds of substitutions and reactions. So, understanding its formula goes beyond textbook knowledge. It stops mix-ups, prevents ruined batches, and keeps your reactions predictable. A simple mistake, like grabbing a different haloalkane, throws off entire projects. Lives in research and manufacturing run on these details.
Why the Numbers Matter
Organic chemistry relies on precision. If you misread the formula, it nudges you toward the wrong chemical. A swapped-out halogen or extra carbon flips a reaction on its head. In a pharmaceutical lab, I once witnessed a batch of painkiller candidates scrapped because someone pulled 1-bromopentane instead of 1-bromohexane. The whole week of work went down the drain—and so did the budget for that project.
Beyond research, thinking through safety is vital. Bromine compounds aren’t always friendly to skin or lungs. The right formula helps you scan the right safety data sheet, set up the proper fume hood, and avoid risky spills. Getting this wrong can mean more than just wasted time; it can land someone in the hospital.
Guarding Against Mistakes
Early in my career, I started double-labeling my bottles and updating inventory lists every week. A few minutes of diligence makes all the difference. The industry needs better tracking of inventory, real-time digital logs, and integrated barcoding to cut down on human error. Clear, useful chemical formulas support digital records as much as they support face-to-face work.
Education helps, but so do habits. Making sure everyone from students to senior chemists recognizes how a simple formula like C6H13Br links to molecular behavior, hazard warnings, and experiment design, reduces risk across the board. Printed lists on fume hoods, up-to-date training, and strong supervision ensure folks don’t confuse chemical siblings.
Bottom Line
A simple label—C6H13Br—carries weight. It guides chemists, shapes safe practices, and keeps production lines running. Bromohexane looks simple at first glance, but its formula is the start of a long chain of decisions, mistakes, and discoveries. Every good science story starts with the right numbers.
Why Bromohexane Deserves Careful Handling
Bromohexane might sound unfamiliar to folks outside chemical labs, but those who’ve worked with organic synthesis know it’s no lightweight. This clear liquid brings alkyl bromides’ usual traits: flammable, toxic, and quick to evaporate. One spilled flask leaves a sting in your nose and a headache that lingers. Years ago, a friend of mine underestimated its fumes, and his cautionary tale has stuck with me since. Lab safety can look like overkill until something goes wrong once.
Proper Storage Means Fewer Headaches
A crowded workbench or a leaky stopper has no place in responsible chemical storage, especially with bromohexane. This chemical reacts with many materials and vapors can worsen asthma or irritate eyes and skin. My old research group kept each bottle locked in a ventilated poison cabinet, set far from heat or sparks, and always away from direct sunlight. Bromohexane’s flashpoint is low. Any stray flame or even a hot plate nearby raises unnecessary risk.
You never want to find out after an incident that the cap wasn’t tight or the shelf wobbled because a shelf collapse can cause two problems at once: chemical spills and fumes. The right storage avoids both. Local fire codes even require protecting flammable chemicals in locked storage rated for combustibles. These rules aren’t there to slow work down—they save property and lives. I’ve seen fire marshals fine labs for carelessness, and that’s nothing compared to the cost of a hospital trip.
Keep Labeling and Inventory Tight
Nothing beats a clear, permanent label on every flask and bottle. This prevents confusion with lookalike solvents—mixing up bromohexane with hexane might sound harmless, but exposure symptoms and environmental impacts differ sharply. Some colleagues keep digital logs of every substance checked in and out. Discipline pays here: no missing stoppers, no faded labels. I remember a less organized lab where unlabeled samples stacked up. One day an intern unknowingly knocked over an open bottle, and the cleanup left everyone jumpy for weeks.
Ventilation and Personal Safety
Storing bromohexane outside a fume hood quickly spreads its smell and risk. My own nose catches even a cracked seal, so I push for lockers with built-in exhaust fans. Personal protective gear tops the list, especially when opening bottles. Nitrile gloves, a lab coat, and safety goggles turn a risky job into routine.
Disposal and Emergency Planning
A responsible storage plan doesn’t stop at the shelf. You want easy access to spill kits, fire extinguishers, and an eyewash station. Experienced teams train twice a year to stay sharp on what to do if a spill escapes the locker. Waste containers stand labeled and locked, ready for professional disposal. Once, a missed drop led to a call with hazardous waste handlers, reminding us all about the cost of taking shortcuts.
Safe bromohexane storage means treating the substance with the respect it commands. Solid routines, strict labeling, and quality containers keep the workspace clean and the team healthy. No shortcut is worth the aftermath.
Understanding the Risks
Bromohexane belongs to a family of alkyl halides, known for their role in organic synthesis. In any chemical lab, it stands out for its toxicity and possible health hazards. A direct whiff often brings irritation to the nose or throat. Touching it with bare skin leaves a red, itchy spot. Breathing in the fumes for a while makes it hard to focus and may trigger headaches or dizziness. From my own training and time around reagents, careless moments taught painful lessons—health takes front seat, especially with these chemicals.
Choosing the Right Gear
Gloves matter most—I always opt for nitrile rather than latex, since halogenated compounds sneak through thinner materials. A decent lab coat, at least knee-length, shields clothing from splashes. For smells this sharp, a fume hood turns essential, not optional. The memory of working in a warm, cramped room with Bromohexane reminds me: wearing eye protection can't be skipped. A splash to the eye can do lasting harm. Safety glasses work for small jobs, but face shields add better defense in bigger projects or awkward setups.
Spill Response and Clean-Up
Accidents follow any routine. Knocking over a flask or tipping a pipette happens fast, even with steady hands. Sand or a spill pillow, not paper towels, gives better results for liquid messes. Sweeping paper towels over Bromohexane just spreads vapors into the air. I keep a container for hazardous solvent waste close, just for moments like these. No one should ever dump Bromohexane in the sink. Waste contractors need to haul off what’s left, or small leaks end up harming the people who rely on clean water or breathable air.
Safe Storage Habits
Old habits can save mistakes. Every bottle of Bromohexane in my old lab always went inside a flammable liquids cabinet with a lock. Ordinary shelves bring risk if containers crack or tip during a rush. The right label—marked with date and hazard—makes sure everyone on the team stays on the same page. I always checked for fading labels or loose lids, since fumes tend to eat away at weak seals. The stories I’ve heard about surprise leaks underline the need for routine checks. It’s better to catch problems early than deal with a bigger mess later.
Emergency Planning
Preparation makes all the difference. My lab conducted drills every few months, with fire blankets and eyewash stations kept up to date. Anyone in the lab should know how to open the shower and use the eyewash within seconds. Fast reaction saves eyesight and sometimes lives. If someone feels strange after handling Bromohexane, I always insist on a trip to the nurse, even if they act tough. Early treatment fights off bigger health scares. For exposure, medical teams benefit when we relay full details—what and how much got spilled—on the spot.
Reducing Risks with Good Practice
Training new staff in person makes more sense than only handing out printed protocols. Hands-on lessons keep safety simple and stick in memory. Good habits, like careful labeling, measured transfers, and steady storage, shrink both accidents and long-term health troubles. Regular refreshers—lessons shared at team meetings or safety talks—keep everyone on alert. You can’t trust luck to protect yourself, coworkers, and the next person who steps into the lab. Relying on smart precautions and collective experience steers things in a safer direction.
| Names | |
| Preferred IUPAC name | 1-Bromohexane |
| Other names |
1-Bromohexane
Hexyl bromide |
| Pronunciation | /ˌbroʊ.moʊ.ˈhɛk.seɪn/ |
| Identifiers | |
| CAS Number | 111-25-1 |
| Beilstein Reference | 1209223 |
| ChEBI | CHEBI:36426 |
| ChEMBL | CHEMBL15471 |
| ChemSpider | 10987 |
| DrugBank | DB08763 |
| ECHA InfoCard | 100.004.315 |
| EC Number | 203-893-9 |
| Gmelin Reference | 11478 |
| KEGG | C06584 |
| MeSH | D001947 |
| PubChem CID | 8075 |
| RTECS number | EO8575000 |
| UNII | R96P7U2V3V |
| UN number | UN2342 |
| CompTox Dashboard (EPA) | DTXSID2021116 |
| Properties | |
| Chemical formula | C6H13Br |
| Molar mass | 165.10 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Odor | Unpleasant odor |
| Density | 1.177 g/mL |
| Solubility in water | Insoluble in water |
| log P | 3.9 |
| Vapor pressure | 0.6 mmHg (at 25 °C) |
| Acidity (pKa) | pKa ≈ 50 |
| Basicity (pKb) | pKb: 4.52 |
| Magnetic susceptibility (χ) | -62.5 × 10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.451 |
| Viscosity | 2.03 mPa·s (20 °C) |
| Dipole moment | 2.60 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | “354.7 J·mol⁻¹·K⁻¹” |
| Std enthalpy of formation (ΔfH⦵298) | -146.7 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -3898.7 kJ/mol |
| Pharmacology | |
| ATC code | R05CB06 |
| Hazards | |
| GHS labelling | GHS02, GHS07 |
| Pictograms | GHS02,GHS07 |
| Signal word | Warning |
| Hazard statements | H302, H315, H319, H335 |
| Precautionary statements | P210, P261, P280, P301+P312, P305+P351+P338 |
| Flash point | 51 °C |
| Autoignition temperature | 170 °C |
| Explosive limits | Explosive limits: 1.1-6.4% |
| Lethal dose or concentration | LD₅₀ (oral, rat): 2,020 mg/kg |
| LD50 (median dose) | 430 mg/kg (rat, oral) |
| NIOSH | RX8575000 |
| PEL (Permissible) | PEL (Permissible Exposure Limit) for Bromohexane: 5 ppm (skin) |
| REL (Recommended) | 24 months |
| IDLH (Immediate danger) | Not established |
| Related compounds | |
| Related compounds |
Hexane
1-Chlorohexane 1-Iodohexane 1-Fluorohexane |
