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Sec-Pentanol: Beyond the Textbooks

Historical Development

Sec-pentanol, a lesser-known member of the alcohol family, has a background that stretches back to the boom in organic chemistry experimentation during the nineteenth and early twentieth centuries. While most spotlight falls on primary alcohols like ethanol or secondary ones like isopropanol, sec-pentanol’s presence in the chemical annals comes down to its structure: a five-carbon chain with the hydroxyl group on the second carbon. Early industrial chemists spotted this structure while searching for new solvents and intermediates. For years, knowledge about sec-pentanol built up slowly through research papers and trial-and-error in labs rather than big news headlines, so only a handful of chemists really understood its value at first. Eventually, synthetic routes became established, and by the mid-century, manufacturing of sec-pentanol moved from theoretical discussions to routine practice in specialty chemicals and fine synthesis sectors.

Product Overview

Sec-pentanol stands as a colorless liquid with a distinctive scent, known in technical circles for its utility as a solvent and intermediate. Compared to more heavily marketed alcohols, it receives less public attention, yet within industrial and pharmaceutical labs, professionals appreciate its role in niche syntheses. Unlike common alcohols that fill supermarket shelves as cleaners or fuel, sec-pentanol occupies a space in the toolkit of researchers who shape next-generation pharmaceuticals, agrochemicals, and materials. The alcohol brings a blend of moderate polarity and reasonable volatility, making it useful for extractions or in compounding processes where too much or too little solubility can cause issues.

Physical & Chemical Properties

In practical context, sec-pentanol boils at a noticeably higher temperature than simple alcohols like methanol or ethanol, hovering around the neighborhood of 118 to 119°C. It comes with a density that places it above water but shy of being classified as a heavy alcohol. Its solubility in water sits between completely miscible alcohols and those with much longer carbon chains – not ideal for dissolving everything, but flexible enough to handle specialized extraction or purification jobs. Chemically, sec-pentanol features the functional group of a secondary alcohol, so it reacts predictably with oxidizers to yield ketones rather than acids, giving it a clear distinction from its n-pentanol cousin. Its moderate volatility means you’ll notice the aroma right away in a lab, and you’ll want proper ventilation whenever sampling or transferring the liquid.

Technical Specifications & Labeling

In a laboratory or manufacturing setting, sec-pentanol usually arrives labeled according to IUPAC or standard chemical names along with a CAS number. It comes packaged in high-density polyethylene bottles or metal drums, sometimes accompanied by safety labeling that highlights flammability and inhalation risks, as these trace back to its alcohol structure. The bottle should carry a clear indication of purity grade—analytical, technical, or food-grade, depending on intended use. Storage often involves temperature control to limit evaporation, and safety data sheets accompany shipments to address risks, mishandling, and disposal guidelines. I have always appreciated the no-nonsense approach that seasoned chemists apply in handling it: gloves, goggles, and a well-ventilated hood have always done the trick, and keeping containers tightly sealed when not in use never gets old as solid laboratory practice.

Preparation Method

Sec-pentanol’s commercial synthesis typically begins with the catalytic hydration of pentenes or through the reduction of the corresponding ketone, 2-pentanone. Industrial-scale production leans toward liquid-phase reactions with supported acid catalysts, a standard method established by trial and error over decades until reliable yields became standard. For a hands-on chemist, small-scale synthesis isn’t outside reach: simple lab setups allow for the reduction of 2-pentanone using sodium borohydride or catalytic hydrogenation. A strong understanding of reaction conditions has always made the difference between a pure yield and a tarry mess, particularly since secondary alcohols can undergo elimination to produce alkenes if the process runs too hot or too acidic. Experienced operators have learned the value of patient distillation and careful temperature control during workup, both to preserve yield and to avoid trace contaminants that throw off future reactions.

Chemical Reactions & Modifications

One of sec-pentanol’s more interesting points lies in its versatility as a synthetic building block. Oxidation with mild agents converts it to 2-pentanone, a stepping stone for perfumes and pharmaceuticals. Dehydration using acid leads to pentenes, which can further participate in addition reactions for the plastics or coatings industries. Halogenation at the secondary carbon allows for the introduction of reactive groups that chemists then use for creating specialty esters or ethers. In my own lab days, I found sec-pentanol an excellent substrate for test reactions when studying the behavior of secondary alcohols in different catalytic systems; secondary alcohols serve as a clear example because their products—a ketone or an alkene—differ from primary or tertiary alcohols. Researchers using sec-pentanol create derivatives that explore everything from plasticizers to new pharmaceutical scaffolds.

Synonyms & Product Names

This alcohol goes by several names depending on the context or the source of the chemicals: 2-pentanol, sec-amyl alcohol, and occasionally methyl propyl carbinol. Many catalogs list it as 1-methylbutanol-2. In trade, I have seen labels favor '2-pentanol' due to IUPAC recommendations, but older documents or reference materials sometimes stick with historic names that reference its structure or origin. Familiarity with these synonyms prevents confusion when cross-checking literature sources or supplier agreements, particularly in global trading.

Safety & Operational Standards

Handling sec-pentanol brings the kind of hazards that come with most small-chain alcohols—flammability, vapor inhalation, and skin or eye irritation. Lab emergencies rarely happen when protocols are respected: fire extinguishers stand ready, and no one ever runs distillations without a splash guard and proper ventilation. Larger facilities tie sec-pentanol use to strict occupational exposure limits based on historical toxicity studies, and experienced hands always label secondary containers. Safety training reinforces that its vapors can catch flame quickly, so open flames or hot plates stay away from work areas. While some operators grow too comfortable with familiar compounds over time, sec-pentanol rewards those who treat it with steady respect. Personal experience has shown that clear labeling, fresh air, and a rigid check of safety protocols prevent most headaches or more serious accidents.

Application Area

Sec-pentanol plays a part in a surprising mix of industries despite its second-fiddle reputation compared to alcohols like isopropanol. In the lab, researchers use it as a solvent for organic synthesis, especially when milder polarity than typical options is needed. Manufacturers blend it in fragrances, where its odor merges well with floral or fruity notes for specialty perfumes and cleaners. Paints, coatings, and even resin systems sometimes call for it to tweak drying times and achieve certain viscosity targets. In pharmaceuticals, chemists use it as an intermediate—its structure makes it useful in multi-step syntheses that demand reliable oxidation or reduction profiles. Smaller agricultural operations use derivatives and esters from sec-pentanol as part of pesticide or herbicide formulations where the right balance between volatility and solubility matters. Sec-pentanol finds its way into adhesives as a carrier or latent hardener. Each of these uses highlights how adaptable this compound can be for those who understand its quirks.

Research & Development

Recent years have brought fresh interest in sec-pentanol, especially in research areas that focus on green chemistry and improved synthetic efficiency. Academic and industry teams study new catalysts and process routes that could lower waste or energy demands. In my view, the push for sustainability makes secondary alcohols like this more attractive because their oxidation products, namely ketones, are valuable on their own. Pilot studies look at flow chemistry methods for sec-pentanol production, hoping to cut byproducts and boost throughput. Analytical chemists have explored sec-pentanol’s role as a reference compound in method validation for chromatography due to its unique balance of polarity and volatility. Interest in sec-pentanol derivatives remains steady as new molecules are sought for niche pharmaceutical or agrichemical applications.

Toxicity Research

Efforts to outline the toxicity profile of sec-pentanol link back to studies on general alcohol safety. Inhalation of vapors leads to headaches and nausea, with longer exposure hitting the central nervous system—a familiar story among volatile organic solvents. Animal studies place sec-pentanol a notch above ethanol in terms of acute toxicity but nowhere near as hazardous as industrial heavy-hitters like methanol or benzene. Chronic exposure data is less robust, but any secondary alcohol taken in large quantities brings metabolic and liver risks similar to isopropanol. Regulatory bodies set workplace exposure limits based on data from controlled trials that simulate industrial settings. Workers who follow basic engineering controls—local exhaust, closed transfers, and regular personal monitoring—stay well below these limits. Those lessons keep reappearing through lab training material and on-the-job reminders.

Future Prospects

Looking ahead, sec-pentanol could capture wider use as industries seek out intermediates that balance performance with lower environmental impact. Companies searching for new solvents that sidestep regulatory red tape on emissions and toxicity see potential in mid-range alcohols like sec-pentanol. Improvements in catalyst design and continuous-flow reactors make it possible to manufacture sec-pentanol with higher yield and less waste, a benefit for companies watching their sustainability scores. Applied research has begun testing sec-pentanol derivatives as potential replacements for solvents under regulatory scrutiny or even as new ingredients in hard-to-formulate consumer products. As the market for bespoke chemicals grows and the demand for greener synthesis takes hold, compounds with the adaptability and manageable risk profile of sec-pentanol may move from backroom specialty to staple order in the years to come.




What is Sec-Pentanol and what are its main uses?

Understanding Sec-Pentanol

Sec-pentanol, known in the chemistry world as 2-pentanol, falls into the group of alcohols. Its structure includes five carbon atoms, giving it a place as a mid-sized alcohol in industrial settings. Most people have never heard of 2-pentanol, but it quietly makes a difference behind the scenes. Factories and research labs get steady use out of it, especially in manufacturing and processing.

Everyday Impact and Industry Role

Sec-pentanol finds work in places you wouldn't expect—think of it as an unassuming supporting actor in industries like paint, coatings, and fragrances. Manufacturers use it as a solvent. It breaks down other chemicals, thins paint, and keeps the workplace running smoothly with its quick evaporation and decent solvency. This quality matters because products require reliable and efficient solvents, especially as industries move away from older, more toxic options like benzene or toluene.

Fragrance companies lean on sec-pentanol to create scents that linger without overpowering. It brings a mild, fresh note to perfumes and air fresheners. In flavoring, a trace of sec-pentanol can be found in some food processes — always tightly regulated for safety, as with all food additives.

Lab Work and Chemical Synthesis

Chemical research labs depend on sec-pentanol for one reason: its versatility. It acts as a starting material for building larger, more complex molecules. In organic chemistry, researchers use it to synthesize flavors, pharmaceuticals, and plasticizers. The process isn't glamorous, but every capsule or bottle on a pharmacy shelf often owes something to the building blocks 2-pentanol helps create.

Sec-pentanol's clear liquid form and moderate boiling point make it easy to handle and distill in controlled lab environments. Lab workers value it because it doesn’t cling to glassware, and it helps create pure samples needed for accurate testing. These physical traits let teams experiment safely and efficiently, which supports innovation in drug discovery and materials science.

Safety and Environmental Responsibility

Safety matters with sec-pentanol, as with any solvent. Exposure can irritate the skin, eyes, or respiratory tract. Factories and labs use tight safety controls, like fume hoods and gloves, to keep people safe. Storage guidelines show clear labels, sealed containers, and proper ventilation come first. These steps help prevent workplace accidents and ensure that health is not jeopardized by carelessness or neglect.

Disposal has become a talking point, especially as environmental standards rise. Sec-pentanol breaks down more easily than many older industrial chemicals. Still, nobody wants traces of solvent in drinking water or local streams. Facilities turn to responsible disposal systems: incineration, or treatment before release, helps meet modern environmental demands and protects the broader community.

Future Steps and Responsible Production

Industry leaders continue searching for greener processes, lower emissions, and alternatives with even less impact on workers and nature. Some manufacturers have updated production lines to lower the carbon footprint or recycle solvent waste. Sec-pentanol production today involves careful monitoring for quality and traceability.

Governments, especially in Europe and North America, keep updating safety rules for production, import, and use. Public health agencies provide clear guidelines on acceptable levels for exposure in workplaces and food products. Everyone from plant manager to warehouse staff gets regular training, which reduces the risk of mishaps and builds a culture that values safety every day.

Final Thoughts

Sec-pentanol rarely gets headlines, but its role matters whether in a research lab, paint factory, or fragrance blend. Balancing effectiveness with health and environmental responsibility, this chemical continues to shape industrial practices and encourages industries to stay alert and adapt to new safety and sustainability standards.

What are the safety precautions for handling Sec-Pentanol?

Why Sec-Pentanol Demands Respect in the Workplace

Sec-pentanol, known as 2-pentanol, shows up in labs and industries from time to time. It gives off a strong odor and burns easily, so it's easy to spot once a spill happens. Anyone who's carried a bottle of this stuff can tell you: it evaporates quickly, can irritate the eyes, and even brief skin contact leaves a tingling memory. These traits make proper handling more than just wise — it keeps people upright and healthy. Over the years, reading accident reports and comparing notes with chemists, I've learned shortcuts just don’t pay off. Safety demands real habits, not just an occasional glove or quick fan in the window.

Personal Protective Gear Changes Everything

Putting on a fresh pair of nitrile gloves before working with sec-pentanol means you skip those nagging rashes and the telltale chemical smell on your hands at lunch. Eye protection matters even more; a small splash might not blind you, but red, burning eyes take the fun out of any day. Chemical-resistant goggles turn a risky step into a routine one. I’ve seen colleagues wear lab coats buttoned up only halfway and regret it as soon as a collar gets damp. A real, nonflammable lab coat fits much better for these jobs.

Work in Well-Ventilated Areas

Opening a container of sec-pentanol in a closed room feels like inviting a headache. The fumes spread, hang, and make breathing less comfortable. Fume hoods do more than just move air around — they reduce exposure by drawing out vapors before they reach your face. Even a small transfer should go inside the hood, with sash low and airflow checked every now and then. If a fume hood isn’t available, setting up portable extraction fans helps, though nothing replaces proper lab ventilation.

Smart Storage and Labeling Avoids Trouble

I remember hearing about someone storing sec-pentanol near oxidizers — the result was a terrifying near-miss. Putting flammable liquids in secure, segregated cabinets keeps flames and sparks far away. Flammable safety cabinets and tight-fitting lids slow down accidents before they start. Every container deserves a clear label, even for the smallest beaker. There’s no excuse for guessing at a mystery liquid later on. Dry, cool spots make the best storage. Drums or bottles should never sit near heat sources — sec-pentanol can ignite below room temperature if given the chance.

Emergency Plans Make a Difference

Accidents with sec-pentanol move fast. If it hits skin, a quick rinse under running water for at least 15 minutes makes all the difference. Eyes need an eyewash station nearby, not down the hall. For fire, a CO2 or dry chemical extinguisher douses flames safely; water spreads burning alcohol. Every workplace benefits from regular drills running through spill response and eyewash use. This is no place for guessing or hoping someone else knows what to do.

Education Beats Overconfidence

Most mishaps stem from hurrying or thinking experience cancels out risk. Safety training isn’t just for new hires. Reviewing chemical hazards and practicing emergency routines — even after decades on the job — helps keep habits sharp. Reading the latest SDS (Safety Data Sheet) offers a reminder of risks that might fade over time. Staying informed builds a workplace where health and safety never fall behind production goals.

Solutions Start with Teamwork

Sec-pentanol won’t get safer just by hoping for the best. Speaking up about worn gear, arranging for hood repairs, and reminding coworkers about proper storage all stack up. Suggesting hands-on drills and giving feedback about safety practices never hurts. Building a culture where people look out for each other might prove the single best measure for keeping everyone unharmed. In my experience, employers who listen to these concerns end up with fewer accidents and a more loyal team too.

What is the chemical formula and structure of Sec-Pentanol?

Getting Familiar with Sec-Pentanol

Most folks don’t spend much time thinking about the difference between one alcohol and the next, but when it comes to chemicals like sec-pentanol, those details start to matter fast. Sec-pentanol stands out from the pack because of its unique placement of the alcohol group. Chemically, the formula reads as C5H12O—meaning five carbon atoms, a dozen hydrogens, and a single oxygen. Scientists often call it 2-pentanol. The alcohol group sits on the second carbon in the chain, giving the molecule its own personality compared to n-pentanol, which tacks that group on the end.

Visualizing Structure and Basic Properties

Drawings help here. Picture five carbons in a straight line. Hook the OH group—the alcohol—onto the second carbon: CH3-CH(OH)-CH2-CH2-CH3. This simple shift away from the end of the chain leads to physical differences. Sec-pentanol tends to have a more noticeable odor than its relatives. It boils at about 119°C, a notch down from similar-sized straight-chain alcohols. Small differences like that point to how a molecule’s shape can punch above its weight.

Experience in the Lab and the Real World

It’s easy to underestimate the need for clarity around chemical formulas and structures, but a few long afternoons spent in a chemistry lab will cure that. Confusing sec-pentanol with its sister compounds could mean unexpected reactions or even safety risks. There are labs that keep safety data sheets handy and mark containers with both the full name and the formula to cut down on mistakes. Sec-pentanol catches fire more easily than many expect—a hazard tied right to its structure.

Why Sec-Pentanol’s Details Make a Difference

Anyone who’s ever worked in industries using solvents or synthesis knows that precision pays. Sec-pentanol shows up as a building block in more complex molecules, perfumes, and pharmaceuticals. In these fields, small shifts in chemical arrangement produce wildly different results. For instance, swapping out sec-pentanol for an isomer with the same formula but a different layout changes solubility, boiling point, and reactivity. Those shifts could mean the difference between a product that works and one that flops.

Addressing Challenges in Chemical Identification

One persistent headache is the confusion that comes from unclear naming or sloppy labeling. There have been times in classrooms or small manufacturing shops where that error led to an experiment failing or hazardous conditions. More robust labeling protocols and regular education on chemical nomenclature reduce risk. In newer industries, reliance on digital inventory tracking systems brings some hope. Barcodes or quick-look databases, used wisely, prevent mix-ups and keep workers safer.

Supporting Future Safety and Understanding

Even though sec-pentanol isn’t a household term, its formula and structure serve as reminders that chemistry rewards careful attention to detail. With accurate information, from clear chemical formulas to straightforward structure diagrams, science becomes less about memorizing rules and more about understanding how small changes echo through a system. Investing in proper education, labeling, and data transparency makes workplaces safer and research more reliable, not just for sec-pentanol but for every compound on the shelf.

How should Sec-Pentanol be stored to maintain its stability?

Understanding the Risks

Sec-Pentanol belongs to the family of alcohols used across different labs and industries. It’s flammable and can give off dangerous fumes if left exposed to air or light for too long. Storing this chemical the wrong way could lead to weaker potency, safety hazards, or even unnecessary health risks. From personal experience in lab settings, I’ve seen what sloppy storage can do—corroded containers, strong chemical odors, and unnecessary headaches for anyone working with the substance.

Keeping Things Cool and Dry

Heat kills stability. Even moderate temperature shifts inside a storage room can break down sec-pentanol, leading to more volatility and accidental leaks. Refrigeration isn't always necessary, but shelves away from sunlight and direct heat sources keep the alcohol intact longer. I found that using climate-controlled cabinets or shaded chemical closets works much better than leaving bottles on open shelves.

Airtight Makes a Difference

Oxygen and moisture creep in quickly if container lids don’t seal tight. Even a few drops of water can react over time, changing chemical consistency and creating unwanted byproducts. Thick glass bottles with ground glass stoppers, lined screw caps, or high-density polyethylene containers cut down exposure dramatically. In busy shared spaces, I always double-check for cracked seals or worn threads before closing up any bottle.

Proper Labeling Goes a Long Way

Mix-ups create real trouble. I once saw sec-pentanol stored in an unmarked plastic jug right next to acetone—a simple oversight, but dangerous. Clear, accurate labeling with both the date of receipt and opening helps everyone keep track of age and stability. Manufacturers often set shelf lives of up to a year if unopened and handled with care, so knowing the date matters just as much as how it’s stored.

Fire Safety Matters

Flammable chemicals need more than just sturdy shelves. If you keep sec-pentanol near hot equipment, electrical panels, or open flames, you stack the odds against yourself. Flameproof storage cabinets with proper vents and grounding lugs make a huge difference. Keep spill kits and Class B fire extinguishers handy. I had a close call once when a loose cap spilled alcohol—luckily, a spill kit was nearby, and disaster was avoided.

Ventilation Has Real Impact

Trapped vapors can turn a storage cabinet into a ticking bomb. Good airflow draws off fumes and keeps concentrations low, especially in smaller labs. Fume hoods or ventilated enclosures cut down on eye and throat irritation, and make accidental release far less likely. Every lab I’ve worked in requires at least some chemical storage under continuous ventilation, especially for volatile organic compounds.

Training Everyone Who Handles It

Even the best storage strategy falls apart if the people using sec-pentanol don’t know the basics. Training goes further than rules on a poster. If someone knows how sec-pentanol reacts to sunlight, moisture, or heat from experience, they won’t leave a bottle cracked open on a busy bench. Frequent reminders and inspection routines help pick up on bad habits before they turn into real problems.

Looking Ahead

As work with chemicals grows, stricter safety rules and better storage technology should follow. More companies offer sensor-enabled cabinets that track leaks and temperature around the clock. Smart labeling and inventory systems reduce mix-ups, and training gets easier with digital reminders. In my experience, the simple basics—a cool, dark place, tight seals, fireproof cabinets, and sharp labeling—build a strong foundation for safe handling and long-term stability of sec-pentanol.

Is Sec-Pentanol hazardous to health or the environment?

Understanding Sec-Pentanol’s Daily Presence

Sec-pentanol, tucked away behind its technical name, crops up in places most folks rarely suspect. This alcohol acts as a solvent, finds work in producing dyes and fragrances, and sometimes pops up in labs. It’s not as famous as ethanol, but sec-pentanol brings its share of risks—both for the people handling it and the creatures and plants outside factory gates.

Breathing and Skin—Where Exposure Happens

People grabbing a bottle of sec-pentanol don’t get a sign warning about health effects. Still, breathing in its fumes or getting it on bare skin can quickly introduce problems. Reports from workers and laboratory incidents point to headaches, dizziness, nausea, and irritation of the nose and throat after inhalation. Touching it can leave red, itchy skin. If swallowed, sec-pentanol acts as a depressant to the nervous system, leading to drowsiness or, at worst, more severe problems like loss of coordination. Experience handling other similar solvents makes it clear—gloves and proper ventilation matter. I’ve watched coworkers tough out headaches after spills. There’s a reason safety data sheets call for cleanup right away and careful labeling.

Fire Hazard Lurking in Everyday Operations

Sec-pentanol doesn’t need much to catch fire. Its low flash point—about 34°C—means it only takes room temperature and a spark. Staying careless with storage or using it near open flames brings a real risk of explosions. Storage rules require proper metal containers, flame arrestors, and grounding, yet stories surface about expensive mishaps when those are ignored. Industry has learned lessons the hard way, so regular folks can take them seriously.

Environmental Spill—Not as Innocent as Water

Anyone releasing sec-pentanol onto the ground or into drains sends a ripple through water and soil. Bacteria may snap some of it up, but not before fish and aquatic bugs run into trouble. Tests show fish struggle when water carries enough sec-pentanol; they lose balance or quit eating. The vapor drifts into the air, where sunlight breaks it down, but the substances it forms—like formaldehyde—aren’t much better. Plants often show wilting or yellowing leaves just from brief exposure. My own days helping clean a small chemical spill near a stream made it clear—animals downstream paid a price quickly.

Solutions—Focus on Minimizing Risk

The only route forward is giving sec-pentanol the respect it warrants. Factories and labs lean on closed systems, local exhausts, and emergency prep. Personal protective equipment works, but only if people treat it as vital, not optional. For environmental safety, secondary containment and real emergency response plans make the difference between a minor scare and lasting contamination. Regular audits mean less chance of carelessness slipping through. Public awareness helps too; limits on dumping and stronger monitoring of chemical use near water speed up recovery.

Science and Transparency for a Safer Path

The hazards aren’t mysterious—enough accidents and studies confirm what happens when sec-pentanol escapes control. Tracking incidents, respecting the science, and sharing what works fill gaps that government rules sometimes miss. Communities near plants want transparency so they know what’s moving through their air and water. Trained experts, up-to-date rules, and honest reporting lay the groundwork for using sec-pentanol with fewer risks to both people and the world outside.

Sec-Pentanol
Sec-Pentanol
Sec-Pentanol
Names
Preferred IUPAC name pentan-2-ol
Other names 2-Pentanol
sec-Amyl alcohol
Methyl propyl carbinol
2-Pentyl alcohol
Pronunciation /ˌsɛkˈpɛntə.nɒl/
Identifiers
CAS Number 584-02-1
Beilstein Reference Beilstein Reference: 1718739
ChEBI CHEBI:15602
ChEMBL CHEMBL16854
ChemSpider 54838
DrugBank DB13941
ECHA InfoCard EC 200-752-1
EC Number 208-760-7
Gmelin Reference 1721
KEGG C02388
MeSH D000371
PubChem CID 6556
RTECS number SA9100000
UNII YNW258QAFZ
UN number UN1265
Properties
Chemical formula C5H12O
Molar mass 88.15 g/mol
Appearance Colorless liquid
Odor Penetrating odor
Density 0.810 g/mL at 25 °C (lit.)
Solubility in water Soluble
log P 0.84
Vapor pressure 3 mmHg (20°C)
Acidity (pKa) 16.0
Basicity (pKb) 15.1
Magnetic susceptibility (χ) -7.72×10⁻⁶ cm³/mol
Refractive index (nD) 1.410
Viscosity 3.905 mPa·s (at 25 °C)
Dipole moment 1.770 D
Thermochemistry
Std molar entropy (S⦵298) 216.7 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -328.7 kJ/mol
Std enthalpy of combustion (ΔcH⦵298) -3337.6 kJ/mol
Hazards
GHS labelling GHS02, GHS07
Pictograms GHS02,GHS07
Signal word Danger
Hazard statements H226, H315, H319, H335
Precautionary statements P210, P233, P240, P241, P242, P243, P261, P271, P280, P303+P361+P353, P304+P340, P312, P337+P313, P370+P378, P403+P235, P405, P501
NFPA 704 (fire diamond) 1,2,0
Flash point 46 °C
Autoignition temperature 220 °C (428 °F; 493 K)
Explosive limits Explosive limits of Sec-Pentanol: "1.1% - 7.5%
Lethal dose or concentration LD50 oral rat 2200 mg/kg
LD50 (median dose) LD50 (median dose): 2400 mg/kg (rat, oral)
NIOSH ST0350000
PEL (Permissible) 100 ppm
REL (Recommended) 0.05 ppm
IDLH (Immediate danger) 400 ppm
Related compounds
Related compounds 1-Pentanol
2-Methyl-2-butanol
2-Pentanol
3-Pentanol