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2-Methyl-3-Ethylpentane: More Than Just Another Alkane

Looking Back: From Early Understanding to Modern Labs

Thinking about how 2-Methyl-3-Ethylpentane first found its way into laboratory glassware leads to a peculiar appreciation of organic chemistry’s steady evolution. Chemists in the twentieth century weren’t handed advanced chromatographs or digital modeling. They pieced structures together with glass columns, simple detectors, and a lot of patience. At that time, decoding branched alkanes took hours over distillation apparatus, and misidentification joined the party more often than anyone wanted to admit. Out of this dogged effort came a sharper understanding of hydrocarbon isomerism—2-Methyl-3-Ethylpentane being a textbook example of how branching swaps around atoms yet evokes big changes in physical behavior. These subtle variations fueled changes in approaches to fuel blending and chemical synthesis, especially as the world shifted from kerosene to gasoline. Many of the gasoline reformulation breakthroughs in the twentieth century can be traced directly to the study of such branched molecules, shifting the balance between performance, safety, and air pollution.

Product Snapshot: What 2-Methyl-3-Ethylpentane Brings to the Table

Most people overlook compounds like 2-Methyl-3-Ethylpentane, whether they spend their days at a refinery, an academic bench, or in product testing. Yet its presence offers technicians and researchers a template for untangling the complexity hidden inside petroleum. Its structure avoids unnecessary flair: a seven-carbon backbone, shaped with one methyl group at the second position and an ethyl group on the third. In routine organic labs, such compounds sometimes appear as standards during chromatographic analysis, ensuring measurements downstream stay precise. Gasoline researchers, particularly those looking at knock resistance, have long turned to branched alkanes like this one to help define the upper reaches of octane performance.

Physical and Chemical Nuances

If you try pouring out 2-Methyl-3-Ethylpentane, you’ll face a clear, colorless liquid. The boiling point lands at a lower number compared to straight-chain heptane. Lower density and higher volatility signal the fingerprints of branching at work, changing everything from evaporation rates to fuel combustion. Ordinary folks might associate this with a pleasant, sweetish hydrocarbon smell, rarely found outside a chemical warehouse. Water shuns it—it’s hydrophobic through and through—and this nonpolarity places it squarely in hydrocarbon territory. Reactivity stays muted in most gentle environments, giving it a reputation for chemical indifference reminiscent of paraffin wax, yet under the right spark, watch out—this is flammable material.

Hands-On Preparation

Synthesis in the lab remains one of those activities where chemists still get a sense of craftsmanship. Creating 2-Methyl-3-Ethylpentane asks for careful alkylation reactions: starting perhaps from lighter alkanes, then relying on Friedel-Crafts chemistry or other catalyzed paths to stitch together the methyl and ethyl appendages onto a pentane skeleton. Industrial-scale processes may look for ways to tune product streams coming out of catalytic crackers or reformers. It rarely gets made on its own for dedicated use, but rather emerges as part of broader hydrocarbon fractions from petroleum. Separating it out then relies on precise distillation and careful quality control, usually handled by experts who balance yield against purity, always hounded by economic and environmental considerations.

Labeling, Synonyms, and Naming Nuances

Anyone who has sorted through bottles on a lab shelf knows confusion over chemical names comes up often. For 2-Methyl-3-Ethylpentane, I’ve encountered synonyms such as 3-Ethyl-2-methylpentane and even less common trivial names, which can lead a novice astray. It enters scientific conversations by its IUPAC designation most reliably, yet research databases, reference books, and supplier catalogs provide a wealth of coded abbreviations and identifiers. This maze underscores why clear labeling—down to the unique CAS number—matters so much for routine safety and research quality, particularly in international trade and regulatory environments where a slip of a name may disrupt an entire supply chain.

Chemical Reactions and Modifications: Not All Hydrocarbons Lie Low

Some might glance at a hydrocarbon and expect little more than dull steadiness, but branching has subtle impacts. 2-Methyl-3-Ethylpentane reacts as an alkane, with strong resistance to acids and bases, yet it combusts cleanly in controlled conditions, transforming into carbon dioxide and water alongside considerable heat. It doesn’t take part in polymerization the way small alkenes do, and under typical lab setups, it won’t join in addition or substitution reactions without some serious coaxing. Subjected to cracking or reforming, its branched structure tends to break more easily under high temperature or catalytic influence, feeding into smaller alkanes or even aromatic compounds. Such reactivity shapes gasoline properties, an area where I’ve experienced plenty of research headaches thanks to the stubborn unpredictability of branched alkane mixtures.

Staying Safe: Risks and Protective Habits

Anyone handling volatile alkanes knows not to take their safety for granted. 2-Methyl-3-Ethylpentane brings the usual set of flammable liquid warnings. Vapors can catch fire from distant ignition sources, and while the smell gives a useful early warning, not everyone has a nose tuned to hydrocarbon risk. Forget to secure containers properly, and evaporation runs wild, filling workspaces with potentially explosive air. Laboratories and manufacturing setups must stick to well-known standards: grounding containers, using explosion-proof equipment, ensuring adequate ventilation and swift cleanup of spills. Skin contact triggers irritation, while long-term high exposure brings headaches and more severe nervous system effects, as shown in animal studies and industrial accident records. Local and international standards expect users to log handling practices and train staff, making drills, physical barriers, and clearly marked zones part of daily operations rather than an afterthought.

Real-World Applications: Not Just Lab Curiosity

Outside the lab, 2-Methyl-3-Ethylpentane rarely steals headlines, but its impact reaches downstream in several industries. Blending engineers at refineries adjust ratios of branched and unbranched alkanes to fine-tune gasoline for efficiency and pollution standards. High-octane numbers from branched alkanes help engines resist knocking, making combustion smoother and safer, and this work shifts quickly into regulatory frameworks that try to protect both engines and public health. For analytical chemists, this molecule joins the ranks of calibration standards, becoming a silent partner in hundreds of oil assays, forensic cases, and environmental monitoring campaigns. In my experience, tracking its fate in complex petroleum distillates teaches student chemists hands-on lessons fast: real samples rarely match theoretical purity, and mixture behavior defies easy prediction.

Research & Development: Pushing What We Know

Recent years saw renewed interest in branched hydrocarbons as advanced fuels, particularly as climate targets tighten around the globe. Teams look toward isomerization, seeking catalysts that swap user demand from simpler compounds to more complex ones able to deliver lower emissions or greater efficiency. Nanotechnology and advanced computational modeling crack open new insight into how branching influences physical and combustion properties, helping to optimize synthetic pathways. I’ve watched as students and experienced engineers alike wrestle with the challenge of accurately predicting boiling points, emission profiles, or even environmental persistence, hungry for models that trim error margins and cut costs. Patents on improved synthesis or analytic detection signal strong industry interest, with researchers often chasing the twin goals of safety and sustainable production.

Toxicity and Environmental Concerns: Minimizing Harm

Toxicology investigations haven’t placed 2-Methyl-3-Ethylpentane in headlines over acute risk, yet that doesn’t mean it sails under the radar. Inhalation studies in laboratory mammals, along with reviews of hydrocarbon exposure in refinery workers, reflect dose-dependent central nervous system effects and respiratory irritation. Its persistence in the environment remains moderate, typical for mid-weight saturated hydrocarbons: spills can smother aquatic surfaces, restrict oxygen transfer, and stress ecosystems if not contained. Regulatory limits for air emissions, effluent, and workplace exposure grew stricter as science peeled back the links between chronic hydrocarbon exposure and long-term health risks. Removing stray hydrocarbons from water, soil, or air demands real investment in monitoring, cleanup technology, and worker training, especially as laws catch up with what science has revealed.

Looking Forward: Role in the Low-Carbon Transition

The next chapter for 2-Methyl-3-Ethylpentane connects directly to society’s appetite for safer chemicals, higher fuel efficiency, and climate responsibility. Chemical engineers shape fuel stocks to meet ever-changing emission standards, and branched alkanes fill a valued slot in unleaded gasoline formulations, providing needed energy without the worst byproducts of heavier or unsaturated hydrocarbons. Researchers now chase bio-based synthetic methods, searching for pathways that skip petroleum, curb carbon emissions, and still deliver branching that boosts fuel quality. Policy shifts and investment in advanced recycling or isomer-specific catalysis signal intent to keep both performance and safety moving upward. As climate science pushes the field toward more resilient, lower-impact processes, compounds like 2-Methyl-3-Ethylpentane become reminders: even molecules that rarely escape the lab or refinery floor play outsized roles in both the challenges and solutions shaping tomorrow’s chemistry and energy.




What is 2-Methyl-3-Ethylpentane used for?

Spotlight on a Lesser-Known Hydrocarbon

2-Methyl-3-Ethylpentane sounds like a tongue-twister most folks left behind in chemistry class. Still, this molecule quietly weaves its way through many corners of our daily life, sometimes without much recognition. As someone who’s spent years following industrial and scientific trends, I can say these hydrocarbons are workhorses of the modern world. They’re far more important than their dry, textbook names suggest.

A Core Part of Gasoline

Let’s start with refineries. Gasoline blends don’t come in “pure” form right from crude oil. They’re made up of dozens of different hydrocarbons, and 2-Methyl-3-Ethylpentane is one of the several branching alkanes inside the mix. Branched alkanes like this one help keep car engines running without knocking and stalling. The higher the octane rating in gasoline, the smoother an engine runs, and 2-Methyl-3-Ethylpentane has a high octane value. Refineries chase these molecules because they deliver on fuel efficiency and engine protection.

From my time speaking with engineers in fuel labs, I learned blending isn’t all about theory and paper calculations. They run through countless tests to check burn rates, emissions, and how each compound holds up in different car models. This molecule is in the mix not by accident, but thanks to years of experience and trial-and-error in fuel performance. Its presence helps limit the chance of pre-ignition, a real concern in older engines and hotter climates.

Making Chemistry Happen

Outside the world of fuel, 2-Methyl-3-Ethylpentane pops up in chemical research and manufacturing. Labs often use it to study how hydrocarbons behave, looking for patterns that can guide everything from plastics recycling to next-generation batteries. Organic chemists rely on these small molecules to probe reaction mechanisms or test new catalysts. When synthesizing more complex molecules, small-branched alkanes serve as controls and references.

Industrial chemistry companies invest time and money producing pure samples of this molecule because researchers expect real consistency. I’ve interviewed chemists who nearly obsess over getting the structure right, since impurities can throw off entire experiments. 2-Methyl-3-Ethylpentane brings reliability, and that reliability drives both small discoveries and big industrial processes forward.

Safety and Environmental Considerations

No discussion about hydrocarbons would be complete without touching on health and safety. This molecule, like many in the alkane family, isn’t especially reactive or toxic under normal use. That doesn’t give it a free pass—workers in refineries or labs still wear respirators and handle even routine compounds with care. Petroleumbased hydrocarbons escape into the air during blending and storage, contributing to ground-level ozone and air pollution. I’ve seen firsthand how community advocates and environmental regulators lean on industry to control leaks and emissions. It’s a tough line to walk between energy demands and cleaner air.

Seeking Better Solutions

Every time new fuel standards roll out, chemists face a puzzle: keep engines working, slash emissions, and use resources wisely. Some are exploring bio-based alkanes, others are tweaking refinery processes to leave less waste. We’ve come a long way from pouring lead into gasoline, but the search for cleaner, smarter fuel continues. 2-Methyl-3-Ethylpentane represents a small part of this puzzle. As pressure builds to address climate change and urban pollution, these molecules will either find new, greener roles—or fade as newer technologies take the wheel.

References:
  • Speight, J.G. (2019). The Chemistry and Technology of Petroleum.
  • U.S. Environmental Protection Agency – Gasoline standards.
  • Personal interviews with refinery chemists and fuel engineers.

What is the molecular formula and structure of 2-Methyl-3-Ethylpentane?

Breaking Down the Name

Chemistry never gets far without a solid grip on names. 2-Methyl-3-ethylpentane immediately looks a bit like a riddle – numbers, roots, and groups all at once. Every bit of the name points toward the way carbon and hydrogen atoms link together. Pentane provides a five-carbon backbone. A methyl group, which sports a single carbon and three hydrogens, hangs out at position two. Over at position three, an ethyl group joins in with its two carbons and five hydrogens. By fitting these pieces together, we arrive at a clear map of the molecule.

Counting the Atoms

Tallied properly, the full formula lands at C8H18. There’s no fluff or ambiguity with this count – eight carbons and eighteen hydrogens make up a saturated hydrocarbon. The molecule doesn’t showcase any double or triple bonds. Drawing it out, the base pentane chain stretches from one to five. Dropping extra groups at the right carbons demands care; a slip can morph the structure into a different molecule. I’ve seen plenty of students get thrown by skipping a beat with these side chains.

Everyday Relevance of Structure

A quick glance might spark questions. Why care about the shape of 2-methyl-3-ethylpentane? Real-life chemistry leans hard on structure. Gasoline, for example, benefits from branching in its hydrocarbons. Branched molecules tend to burn more evenly and resist knocking in car engines, keeping transportation running smoothly. The compact, branching pattern in 2-methyl-3-ethylpentane tells us it’ll behave differently from its straight-chain cousin, octane. That’s a small, telling detail that engineers watch closely. The structure isn’t just a classroom puzzle — it’s tied to fuel performance, efficiency, and long-term engine health.

Learning from the Details

Many of us encountered hydrocarbon structures early in our studies. I remember fiddling with model kits, trying to place those stubby methyl and ethyl groups onto a stiff pentane backbone. Those hands-on attempts cemented the lesson: one misplaced carbon changes everything. 2-Methyl-3-ethylpentane isn’t the only branched isomer of octane, but its specific pattern gets a chemist’s attention due to how branching affects boiling point and combustibility.

Branched hydrocarbons like this one often see use in industrial processes beyond fuel. Lubricants, solvents, and specialty chemicals sometimes rely on carefully chosen molecules for specific tasks. The more we know about the structure, the tighter our control over performance.

Improving Understanding and Application

Building comfort with molecular structures goes beyond exams and textbooks. Visualization tools, model kits, and software that allow for the rotation and manipulation of molecules make a real difference in understanding. For professionals and students alike, putting in the time to master these relationships adds clarity when approaching both routine and cutting-edge chemistry.

Clear, structured naming and accurate, hands-on modeling bridge the gap between the lab bench and daily products. The story of 2-methyl-3-ethylpentane circles back to that ongoing lesson: small changes in arrangement drive huge shifts in properties and usefulness. For anyone working with organic molecules, keeping an eye on each group and bond never loses its value.

Is 2-Methyl-3-Ethylpentane hazardous to health or the environment?

What We Know About 2-Methyl-3-Ethylpentane

Few people outside chemical engineering circles talk much about 2-Methyl-3-Ethylpentane. It’s another hydrocarbon that shows up most often as part of the complex mix in gasoline or industrial solvents. Most folks bump into it only through emissions or working environments. It belongs to the family of alkanes, which means it isn't especially reactive, but that doesn’t make it harmless.

Personal Encounters with Hydrocarbons

On the job in an older machine shop, the smell of evaporating hydrocarbons drifts through the air with every wipe-down of machinery. Many of us don’t think about what’s in those fumes, but years in that environment add up. Headaches, dizziness, or mild irritation can crop up after a hectic day. Stories circle about workers who cut corners because “it just smells like gasoline.”

Science sheds light on what happens in our bodies when we breathe these vapors in: hydrocarbons can affect the central nervous system, especially in poorly ventilated rooms. Long-term exposure raises the risk. OSHAs guidance and the experience of countless shop crews point in the same direction: get plenty of airflow, wear protection, and stay informed about what’s swirling in the air.

Environmental Concerns Are Easy to Miss

Environments take the hit from hydrocarbons like 2-Methyl-3-Ethylpentane too. When spilled or leaked, this chemical doesn’t hang out in the soil for long—it evaporates fast. Trouble is, that vapor heads straight for the atmosphere. Out in open air, sunlight can break these molecules down into ground-level ozone. Ozone down here triggers respiratory problems and adds to the mess known as smog.

Wildlife and plants don’t escape untouched. Small leaks from storage tanks may seep into groundwater. Once underground, hydrocarbons can stick around for a long time, making cleanup tough and expensive. My neighbors near an industrial site fought for months over a hydrocarbon plume that led to water well testing, bottled water deliveries, and sleepless nights.

Facts, Not Just Feeling

Little research singles out 2-Methyl-3-Ethylpentane apart from its more notorious hydrocarbon cousins. No headlines warn about it, but chemical safety data sheets say, in plain language, that it can bother eyes and lungs and cause drowsiness. The U.S. Environmental Protection Agency flags volatile organic compounds like this as contributors to urban air pollution. And health agencies don’t mince words about what repeated inhalation can do: long-term effects, ranging from breathing problems to impacts on the nervous system, are well documented for hydrocarbons as a group.

Room for Solutions

Basic steps go a long way. Proper storage and handling cut down on spills and leaks. Regular air checks in workplaces keep exposure down. Switching to less volatile chemicals, where possible, lightens the burden on both workers and the surrounding community. I’ve seen local governments band together with industry to monitor air quality near chemical sites; cooperation can mean faster action and less risk for everyone. If you live or work near facilities that use these sorts of chemicals, ask about their ventilation, storage, and safety protocols.

Ignoring the risks doesn’t make them go away. A straightforward conversation about the chemicals we use and the habits we keep leads to safer workplaces and cleaner neighborhoods.

What are the storage and handling recommendations for 2-Methyl-3-Ethylpentane?

Understanding the Substance

2-Methyl-3-Ethylpentane shows up in many labs and industrial settings as a colorless, flammable liquid. It comes from the family of alkanes—compounds made up entirely of hydrogen and carbon. The public rarely hears about it, but in chemical plants, solvent stores, and certain research projects, people cross paths with it daily. Handling this chemical correctly means safety, not just for yourself, but also for coworkers and the surrounding environment.

Fire Risk and Safety Measures

This chemical catches fire easily. The flash point lands below room temperature, so vapor in the air can ignite after just a small spark. Forgetting this fact, or letting safety checks slide, easily leads to fire or explosion. The most direct way to manage the risk: keep containers tightly sealed, label them clearly, and remove sources of static or open flames from the storage space.

I’ve seen facilities let things pile up—rags, cardboard boxes, random tools—near their solvent shelves. Not only does this create trip hazards, it makes fighting a fire nearly impossible. Clean and uncluttered storage spaces matter. Ventilation prevents vapor buildup, so install local exhaust if the room feels stuffy. If someone ignores this, the strong oily odor tells them when vapor levels get too high. Trust your senses.

Container Choices and Storage Conditions

Don’t use just any container. Only steel drums or cans designed for flammable liquids work well. Polyethylene sometimes softens after long contact with hydrocarbons like 2-Methyl-3-Ethylpentane. Spilled liquid shouldn’t sit on the floor—use spill trays under drums and keep absorbent material nearby for cleanup.

Drums go on solid, flat shelving down low—not stacked up high or right next to an exit route. Avoid direct sunlight or heat sources, since temperature swings boost the evaporation rate and pressure inside containers. Many companies add fire-rated cabinets so one mistake doesn’t threaten the entire site.

Health Precautions

Breathing in too much vapor leads to dizziness, headaches, or worse symptoms. Basic safety practices offer a shield here: chemical splash goggles, nitrile gloves, and long sleeves keep skin and eyes protected from splashes or drips.

Read the safety data sheet before pulling the first sample. This shouldn’t get tossed aside like a piece of fine print. Anyone handling the solvent must know where eyewash stations and safety showers are located. In smaller spaces—think universities or startups—a disposable respirator might be the extra step needed if air levels creep higher than safety guidelines allow.

Environmental Protection and Disposal

Spills run straight into drains if no controls exist. Block those off ahead of time and track all liquid waste by labeling containers. Send hazardous waste only to approved disposal sites, never down a sink. In some labs I’ve visited, neglecting these steps led to expensive cleanup by environmental agencies.

Good recordkeeping stands as a guardrail for chemical safety. Training refreshers keep everyone ready for the occasional slip or spill, making sure hazards stay contained. These small steps, repeated daily, hold the line between routine work and a full-blown emergency.

Where can I purchase high-purity 2-Methyl-3-Ethylpentane?

Not Just Any Chemical Buy

Shopping for specialty chemicals like 2-Methyl-3-Ethylpentane often takes more than a quick online search. Scientists and engineers working in labs, oil analytics, or materials synthesis know purity separates successful experiments from failed ones. My time working in a university research group taught me to mistrust cheap, gray-market options for chemicals that seem obscure or hard to find. Contaminants can throw entire projects off, waste weeks of work, and drain budgets.

Reputable Chemical Suppliers: Reliability Over Convenience

High-purity grades demand attention to supply chain and storage conditions. Reputable chemical suppliers like Sigma-Aldrich (MilliporeSigma), Thermo Fisher Scientific, Alfa Aesar, and TCI America offer documented purity, origin details, and clear safety data. Each of these companies has a track record across decades, with certifications that global industries rely on. Product batches come with downloadable certificates of analysis that back their quality claims, not just marketing messages.

Ordering from these sources means going through some hurdles, especially if dealing with chemicals less common than solvents like acetone. Most high-grade 2-Methyl-3-Ethylpentane options show up in protected B2B catalogs rather than consumer-facing storefronts. Expect to fill out paperwork about intended use and affiliation, and sometimes, regulatory checks to ensure safe and lawful end use.

International Procurement: Challenges and Risks

Global sourcing has made rare chemicals somewhat easier to find, but risks climb when deals stray from established suppliers. In the past, colleagues attempted to buy through no-name web storefronts or international third-party distributors that promise overnight shipping at suspicious discounts. Purity claims, origin, and even chemical identity can’t be confirmed in such cases without dedicated lab equipment. There are stories where untested product batches derailed key research or, worse, introduced hazards to the lab.

Shipping restrictions also come into play. 2-Methyl-3-Ethylpentane belongs to the hydrocarbon family, and falls under regulations for flammable and volatile substances. That affects how it ships, what documentation is needed, and which carriers handle the process. Large-scale buyers usually handle this through dedicated compliance teams, but solo researchers and small labs must double-check all paperwork and import rules before payment.

Why Purity Standards Matter

The difference between laboratory grade and technical grade often defines whether a result will stand up in peer-reviewed research or high-standard manufacturing. Even trace impurities in solvent mixtures can skew chromatography runs or chemical syntheses. As a former chemistry graduate student, I remember supervisors carefully vetting suppliers; a quick impurity — even at parts-per-thousand — meant thousands of dollars lost through failed samples and repeated experiments.

Chemical safety must not get overlooked either. Genuine labels, sealed containers, and clear hazard data protect the people handling the chemical and the environment around them. No highly purified sample is worth the risk of accidental poisoning, fire, or environmental release due to a counterfeit or mishandled delivery.

Addressing Accessibility and Alternatives

It’s valid to note how resource-intensive this process still feels for small labs, educators, or researchers in underfunded institutions. Some collaborative buying networks and academic consortia pool resources to bulk order specialty chemicals, reducing cost and paperwork per lab. For non-lab or industrial applications, users may consider if substitutes or less regulated compounds would work — though that decision always comes after consulting with technical experts, not out of convenience or cost-cutting.

Safe and consistent access to specialty chemicals like 2-Methyl-3-Ethylpentane comes down to working with proven suppliers, checking documentation, and planning for regulatory steps. Saving money or time rarely pays off when precision and safety are on the line.

2-Methyl-3-Ethylpentane
2-Methyl-3-Ethylpentane
2-Methyl-3-Ethylpentane
Names
Preferred IUPAC name 3-Ethyl-2-methylpentane
Other names Diisopropylmethane
Pronunciation /tuː ˈmɛθ.əl θriː ˈɛθ.ɪl ˈpɛn.teɪn/
Identifiers
CAS Number 1071-59-4
Beilstein Reference 1108734
ChEBI CHEBI:131222
ChEMBL CHEMBL158356
ChemSpider 15390
DrugBank DB14109
ECHA InfoCard DTXSID70228574
EC Number 205-254-5
Gmelin Reference 108086
KEGG C11244
MeSH D017890
PubChem CID 12045
RTECS number MK9425000
UNII FS630WLV77
UN number UN1208
Properties
Chemical formula C8H18
Molar mass 100.205 g/mol
Appearance Colorless liquid
Odor gasoline-like
Density 0.703 g/cm³
Solubility in water Insoluble in water
log P 3.83
Vapor pressure 1.4 kPa (at 25 °C)
Acidity (pKa) pKa ≈ 50
Basicity (pKb) Non-basic
Magnetic susceptibility (χ) -74.6·10⁻⁶ cm³/mol
Refractive index (nD) 1.397
Dipole moment 0.13 D
Thermochemistry
Std molar entropy (S⦵298) 389.6 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -204.6 kJ/mol
Std enthalpy of combustion (ΔcH⦵298) -4119.7 kJ/mol
Hazards
GHS labelling GHS02, GHS07
Signal word No signal word
Hazard statements H225, H304, H336, H411
Precautionary statements P210, P233, P240, P241, P242, P243, P261, P271, P273, P301+P310, P303+P361+P353, P304+P340, P331, P370+P378, P403+P235, P501
NFPA 704 (fire diamond) 1-1-0
Flash point Flash point: -18 °C
Autoignition temperature 438 °C
Explosive limits Upper 5.4%, Lower 1%
Lethal dose or concentration Lethal dose or concentration: LD50 (rat, oral): > 2000 mg/kg
LD50 (median dose) LD50 (median dose): Oral rat LD50 > 5000 mg/kg
PEL (Permissible) Not established
REL (Recommended) 0.1 ppm
Related compounds
Related compounds 2-Methylpentane
3-Ethylpentane
2,3-Dimethylpentane
3-Methyl-2-ethylpentane
Hexane