1-Octanethiol: A Deep Dive into Its Past, Properties, and Future
Historical Development
Stepping back in time, 1-Octanethiol did not show up out of nowhere. Chemists tracing the lineage of organosulfur compounds found themselves drawn to thiols because sulfur’s tendency to bond with carbon offers a whole range of chemical quirks. In the early days, researchers investigating smelly molecules found in crude petroleum stumbled across 1-Octanethiol alongside other alkanethiols. By the mid-20th century, as organic synthesis advanced and folks started caring more about building functionalized surfaces for devices and medical tools, 1-Octanethiol went from being another stinky liquid to a compound of growing relevance. People started looking at this molecule as more than just a curiosity, noticing that its straight-chain structure and reactive sulfur made it a solid fit for newer technologies that depend on self-assembled monolayers and surface chemistry.
Product Overview
In the current chemical landscape, 1-Octanethiol sits as a colorless liquid with a potent, often unpleasant odor. It contains an eight-carbon chain ending in a thiol group, which puts it in a rare class of organosulfur compounds. Labs and industry pull it off the shelf not for the smell but for that combative S–H group, which stands ready to react with gold surfaces, metal oxides, or participate in all sorts of organic synthesis. Suppliers bottle 1-Octanethiol tightly, aware that even trace exposure to air can produce fumes best left outside the laboratory.
Physical & Chemical Properties
Peer into a vial of 1-Octanethiol and you’ll see a nearly water-clear liquid that evaporates quickly, with a boiling point touching 194°C and a melting point just above freezing. With a density just under that of water, it doesn’t float or sink so much as hover when poured into other solvents. The strong, skunk-like odor is thanks to that SH group; for all its irritation, this trait signals high volatility and warns users before accidental exposure. Chemically, 1-Octanethiol bends toward nucleophilic reactions, reaching eagerly for electrophilic partners. It resists breaking down under neutral conditions but reacts swiftly with oxidizers or in the presence of strong acids and bases. Despite the unassuming appearance, the reactivity of that end-group turns this molecule into a valuable toolkit item for those who need sulfur’s special touch.
Technical Specifications & Labeling
Manufacturers list CAS number 111-88-6 on every bottle. Product purity generally hovers around 98%, sometimes higher for specialty use in electronics or pharmaceuticals. Labels include hazard pictograms warning against inhalation and skin contact. Storage instructions persistently warn about keeping 1-Octanethiol in tightly closed containers, tucked away from sources of ignition and sunlight, as the volatility and pungency can turn a slip into a full-blown fire drill. Documentation lists boiling point, melting point, flash point (often around 76°C), and solubility (insoluble in water yet mixes well with organic solvents), with reference to recommended personal protective equipment.
Preparation Method
Industrial production usually starts from 1-chlorooctane or octanol, which undergoes nucleophilic substitution with hydrogen sulfide or sodium hydrosulfide, often catalyzed by bases in polar aprotic solvents. The process may produce a mix of linear and branched thiols unless carefully controlled. Smaller labs preparing research quantities tend to prefer hydrosulfide routes for fewer byproducts, using distillation under inert atmosphere to isolate pure 1-Octanethiol. A chemist handling the crude product learns the importance of fume hoods and effective lab ventilation—no one wants an afternoon spoiled by sulfur vapor.
Chemical Reactions & Modifications
The S-H bond on 1-Octanethiol proves especially reactive. On gold or other noble metal surfaces, the thiol end forms robust bonds, letting researchers construct monolayers with tuned electrical or chemical functions. Modifications span from simple oxidation—producing disulfides or sulfonic acids—to more complex alkylations or acylations when building longer molecules. Combining the octanethiol with functionalized alkyl halides extends its reach, sometimes serving as a stepping stone toward polymers or surfactants. Oxidants like hydrogen peroxide convert the thiol to the corresponding sulfonic acid, which changes its behavior in solution and alters its value in catalysis or separation chemistry.
Synonyms & Product Names
Not everyone calls it 1-Octanethiol. Dig through catalogs or databases and synonyms like n-Octyl mercaptan, Octylthiol, or 1-Mercaptooctane pop up. Some suppliers bundle it under system names, including their private labeling, but seasoned chemists always check for the classic CAS 111-88-6 to stay on target.
Safety & Operational Standards
Contact with 1-Octanethiol risks both acute irritation and long-term health problems if handled carelessly. The stench alone drives most people to use double gloves, splash goggles, and, if possible, double-layered lab coats. Unventilated spaces quickly fill with the foul odor, indicating a need for fume hoods or closed transfer systems in industrial settings. OSHA and REACH guidance require clear labeling, training for workers, ready-to-go spill kits, and strict handling protocols. Fire risk climbs when vapors collect near ignition sources, so static control, grounded containers, and routine air quality monitoring stay high on the priority list.
Application Area
Engineers and researchers pull 1-Octanethiol into action for surface modification jobs, especially on gold nanoparticles and microchips. It turns up in biosensor fabrication, offering a simple way to attach single layers of molecules as sensors for toxins or microbes. Electronics and photovoltaic manufacturers value its ability to tune surface energy and create hydrophobic coatings. Some organic synthesis workflows depend on 1-Octanethiol as an activator or reactant in building complex molecules, especially those that benefit from sulfur’s unique chemical profile. Its presence in lubricant additives and specialty surfactants shows up in small but crucial places, often out of the public eye.
Research & Development
1-Octanethiol earns a steady spot in R&D pipelines, mostly for its cooperative chemistries. Chemists at the frontier of nanoengineering rely on its ability to produce uniform, self-assembled monolayers for advanced device fabrication, biosensors, and miniaturized electronic components. Ongoing studies investigate how modified surfaces outperform standard hardware in medical devices, corrosion protection, and even wastewater treatments. In academic research, people tinker with new derivatives of 1-Octanethiol for improved stability, broader functional ranges, or more environmentally friendly breakdown products. As the electronics industry presses for faster chips and more reliable sensors, research around thiol-terminated molecules continues to attract attention and investment.
Toxicity Research
Toxicologists exploring the health effects of 1-Octanethiol flag its low acute toxicity but urge caution due to chronic exposure risks. Even small spills in the lab lead to headaches, eye irritation, and respiratory discomfort, highlighting a need for strong ventilation and limited exposure time. Animal studies suggest moderate oral toxicity, though the body metabolizes it fairly quickly compared to heavier thiols. Researchers remain concerned about the environmental impact, as discharges into waterways may threaten aquatic organisms at low concentrations. Environmental scientists recommend robust waste treatment for emissions of organosulfur compounds, and regulatory agencies push for tighter tracking and control.
Future Prospects
Looking ahead, 1-Octanethiol won’t vanish from lists of essential lab chemicals any time soon. Engineers developing next-generation biosensors, nanomaterials, and smart coatings continue to find new uses for its unique structure. With industry moving toward environmentally safer practices, future efforts will likely focus on making and recycling 1-Octanethiol with lower emissions, higher atom economy, and fewer hazardous byproducts. As artificial intelligence and machine learning accelerate molecular design, researchers expect to discover thiol-based compounds with even better performance. Environmental chemistry points toward the need for green synthesis and better end-of-life management, ensuring that continued use of 1-Octanethiol can support innovation without piling up chemical waste. In the ongoing search for materials that can both perform and protect, this sulfur-tipped molecule keeps its place in the conversation—and the laboratory bottle rack.
1-Octanethiol: More Than Just a Chemical Name
1-Octanethiol doesn’t often make headlines, but those working in labs or involved in materials science bump into its sharp, onion-like scent pretty quickly. This substance, made up of eight carbon atoms and a sulfur group, finds its way into places most people rarely think about. Like a lot of sulfur compounds, it tends to stand out — sometimes because of its strong odor, sometimes because of the impact it has behind the scenes, especially in chemistry research and manufacturing.
Why Chemists Reach for 1-Octanethiol
One of the biggest reasons people rely on 1-Octanethiol comes down to how well it helps create “self-assembled monolayers” on metal surfaces, especially gold. This process sounds high-tech, but in practice it’s a bit like using Velcro: the sulfur part sticks tightly to metal, and the rest of the molecule sticks up, making a neat layer just one molecule thick. In experience, these films go a long way in protecting metal, studying cell behavior, or building sensors. Researchers shaping the tiniest switches and sensors for electronics often start with these monolayers.
Working in a research lab, I’ve seen students spend hours cleaning gold slides, pipetting 1-Octanethiol, and watching as thin films slide into place. This step can shape whether an entire experiment works or doesn’t. These films create a surface scientists can “tune” by changing the molecule—making it slippery, sticky, water-loving, or water-hating, all based on tweaks to the chemical recipe.
Beyond the Lab Bench
1-Octanethiol’s value doesn’t stop at the research stage. It also shows up in the world of coatings, helping to keep products free from corrosion or to guide liquid patterns in microfluidic devices. In the realm of nanotechnology, this chemical helps piece together gold nanoparticles for improved medical tests and drug delivery systems. The strong connection it makes with gold lets engineers put together reliable devices, from glucose finger-prick sensors to the test strips used in disease detection.
Some industrial chemists mix it into processes for making specialty chemicals, especially when a project needs the unique properties that only sulfur can bring. It’s even found modest applications in synthesizing flavor ingredients, though only after rigorous purification since nobody wants that intense, questionable aroma in their food.
Potential Concerns and What Workers Do About Them
Sulfur chemicals demand caution. 1-Octanethiol fumes can irritate the nose, throat, and eyes—sometimes badly enough to halt work in a busy lab. Gloves, fume hoods, and careful waste disposal rank up there with goggles. In shared group spaces, workers complain more about the smell than the risk, but both matter. In industrial settings, leaks or spills call for fast action and solid cleanup routines.
Long-term exposure to sulfur compounds raises extra questions. Some worry about effects on air quality inside busy facilities, especially in places without strong ventilation. Companies invest in air monitors and staff training to keep risks down. Regulatory guidance sets hard rules on how much vapor a person can safely breathe. Over the years, safety data and government oversight have sharpened practice.
Improving Applications and Reducing Risks
Making 1-Octanethiol easier to handle and minimizing waste would mark a big win. Some newer research probes how to replace the thiol chemistry with more environmentally friendly options, but for many advanced electronics jobs, few substitutes stick as well to gold. Looking at ways to capture or neutralize its strong odor, labs experiment with filters and closed systems.
With all its quirks and challenges, 1-Octanethiol keeps showing up in places where invention happens. Its standout properties make it a quiet partner in science and manufacturing, shaping new products even as its smell keeps chemists wide awake.
The Structure Behind 1-Octanethiol
1-Octanethiol carries the chemical formula C8H18S. This compound forms by taking an eight-carbon alkane, octane, and replacing one hydrogen from the terminal carbon with a sulfur atom bonded to hydrogen. Chemically, it’s recognized for the functional group –SH, known as the thiol group, attached to the end of a straight-chain hydrocarbon. The structure looks simple at first glance, though its uses and the reasons people research it stretch beyond a few textbook lines.
Why Does This Compound Matter?
I spent years working in academic and industrial labs, sometimes finding myself wrestling with strong-smelling chemicals. 1-Octanethiol is famous for its potent odor, which lingers longer than most people can tolerate. Such aroma gives you a built-in safety signal; you notice spillage before it becomes a bigger problem. On a structural level, the presence of the thiol group changes everything. It transforms what would be a standard oily hydrocarbon into a molecule with distinct reactivity. Sulfur bonds open doors to joining chains, making coatings, and capping gold nanoparticles in research. Nanotechnology circles trust thiols to anchor molecules to metal surfaces because the sulfur atom binds tightly to gold, silver, and other noble metals.
Practical Relevance in Research and Industry
Anyone working with organic synthesis sees the value in simple thiols like 1-Octanethiol. It finds its way into the toolkit for organic chemists who want to make new sulfides and disulfides. Lab notes will often highlight how a thiol group helps produce a molecular handle, allowing further chemical tinkering. Most gold nanoparticle functionalization relies on these sulfur bonds for stability and longevity in diagnostics, cancer research, and sensor development. I remember the day a shipment arrived with octanethiol. We could tell, well before the delivery guy finished unloading, that octanethiol had entered the building. That strong, memorable scent—love it or hate it—also means you typically don’t forget to treat it with respect.
Potential Issues and How to Address Them
Strong-smelling compounds like 1-Octanethiol need strict controls. Prolonged exposure creates both discomfort and risk, especially in poorly ventilated spaces. Safety data sheets stress the importance of fume hoods and personal protective equipment. Gloves and safety goggles should be a habit, not an exception. Storing thiols in sealed bottles, away from acids and oxidizing agents, prevents hazardous reactions. For those disposing of unwanted samples, hazardous waste streams are the only option. Never pour it down the drain—local wastewater regulations specifically mention organosulfur compounds because of their risk and persistence in the environment.
Looking Forward: Safety and Sustainability
Society depends on researchers, manufacturers, and waste handlers to treat chemicals like 1-Octanethiol with seriousness. Clear labeling and proper ventilation prevent most incidents. Substituting less volatile or less pungent thiols, when possible, helps reduce workplace complaints and exposure. In green chemistry circles, people keep looking for new ways to achieve the functionality of thiols without their signature drawbacks. Industry pushes for sustainable sourcing and cleaner disposal, aiming to shrink the ecological footprint. Community input plays a role, as odor concerns from manufacturing sites often drive tighter monitoring and reporting standards. As research continues, the value of solid chemical knowledge, paired with hands-on safety practices, keeps workers, communities, and the environment safer.
Understanding 1-Octanethiol
1-Octanethiol usually pops up in labs focused on organic chemistry, nanotechnology, or coatings. This clear, oily liquid gives off a strong, unpleasant smell, and for those who’ve handled it, that odor lingers no matter how careful you are. Sitting down to talk storage, I always urge folks to build habits that protect their health, research outcomes, and any shared lab space. Nothing messes up teamwork quicker than a leaking bottle of thiol in the corner. Worse, this stuff reacts with air, sparks, and many common lab chemicals.
Health and Safety Take Priority
Working around 1-Octanethiol means treating it as hazardous, no debate needed. Eyes and lungs can only handle so much—one careless moment leaves hands smelling foul for days. According to the International Agency for Research on Cancer, thiols have a history of irritating skin and eyes, and some people develop chemical sensitivities after repeated exposure. Anyone who values their well-being takes gloves, goggles, and a coat seriously. If spills happen, ventilate the space right away and get rid of anything contaminated. Long-term, even small spills can corrode surfaces or linger in the air.
Best Space and Conditions
You won’t catch experienced chemists keeping 1-Octanethiol on an open shelf. This liquid belongs in an airtight, glass or Teflon-lined bottle with a firm seal, kept inside a metal flammables cabinet. Dark corners keep sunlight away—the compound breaks down if left in direct rays. I once saw an old container left out in the sun at a field site; within weeks, the seals decayed and the bottle leaked out a sharp stink.
Local fire codes demand flammable liquids be separated from acids, oxidizers, and basic solutions. A good storage spot stays dry and cool—anything warmer than room temperature makes vapors build up, and 1-Octanethiol can ignite pretty easily if mixed with air. Keep the bottles off the ground and on spill containment trays for a quick cleanup if leaks happen.
Labeling and Inventory Matters
Rushing through labeling creates a different risk—mixing up bottles or underestimating shelf life. Each bottle should display the name, concentration, date received, and expiration. Lab inventory checklists help prevent forgotten containers from sitting past their prime; degraded 1-Octanethiol produces more vapor and becomes a headache—literally and figuratively. Some universities and factories run mandatory inventory checks every quarter, and for flammable chemicals, nobody complains about overkill.
Safe Handling and Community Training
Even with good storage, a training session beats a thousand warning stickers. Regular drills on spill cleanup, using safety showers, and disposal rules cut down on avoidable accidents. Real stories stick—a friend once described a drop on a glove chewing through to her wrist in minutes. That story left a bigger impression than a list of guidelines. Teaching everyone, not just senior scientists, how to spot problems makes labs and workshops safer for everyone.
Final Thoughts on Responsible Care
Caring for 1-Octanethiol doesn’t stop at the storage door. Old material must go into clearly marked waste cans. Many places partner with certified chemical disposal services, since dumping this down the drain leads to environmental fines and spoiled water systems. Rules come from mistakes made by earlier generations, and a little vigilance means today’s researchers and workers don’t lose time or health to something so easy to avoid.
Sharp Odor, Strong Effects
Working with 1-octanethiol isn’t something people do every day, but in labs and certain industries, it pops up often. This colorless liquid brings a powerful odor reminiscent of rotten eggs — a real stink that sticks around. The smell alone makes folks reach for their gloves, but protecting your nose isn’t enough. This stuff carries health risks that deserve attention, and ignoring safety in its presence has real consequences.
Personal Experience: Lessons Learned in the Lab
I remember the first time I found myself on a university bench working with thiols. Our supervisor drilled home the importance of goggles, nitrile gloves, and proper coats. A drop on the bench needed fast cleanup, or the smell would punch its way through the whole wing. It’s not just about comfort. The skin burns and headaches some coworkers reported from sloppy handling spoke for themselves. People tried shortcuts, thinking they’d get lucky for one experiment; nobody stayed lucky for long.
Why Ventilation Isn’t Optional
The safety data sheets call for strong ventilation. After a decade in chemical research, I’ve seen cases where working under a fume hood transformed the experience. Without it, the vapors hit you hard — burning eyes, a scratchy throat, and worse if you aren’t careful. Folks often forget that 1-octanethiol vapors catch fire easily. Open flames or sparks spell trouble, so keeping sources of ignition away from workspaces becomes a habit. From firsthand experience, one forgotten Bunsen burner forced an evacuation and left an impression no one forgot.
Clean-Up Can’t Wait
Spills with 1-octanethiol demand action. I’ve seen people look for paper towels or just fan the air. That’s not enough — this chemical seeps into surfaces and lingers, and the more it spreads, the tougher it gets. The right way means using absorbent materials, sealing them in bags, and reporting the spill every time. Putting off cleanup or skipping the paperwork often leads to more headaches down the line, especially if the residue ends up on someone’s skin.
Protecting the People Doing the Work
Occupational health standards demand respect in workspaces using 1-octanethiol. Employers have to supply enough gloves, goggles, and full-length lab coats. Regular training lets newcomers see why those steps matter. Locking chemicals in secure cabinets cuts down on accidental exposure. Clear labeling and routine inventory checks backstop even the most careful team. One lab I worked in started using color-coded storage for hazardous materials — the visible reminder guided better habits for everyone, whether they knew the chemistry or not.
Health Effects: Taking Symptoms Seriously
Nausea, drowsiness, and shortness of breath can signal real trouble after exposure. It’s easy for new workers to brush off lightheadedness as fatigue, but in my experience, reporting symptoms early led to faster solutions and fewer long-term problems. Emergency showers and eyewash stations need to stay unblocked and ready. In one case, a quick rinse after an accidental splash meant a minor scare instead of a hospital visit.
Simple Steps Make a Difference
Dealing with 1-octanethiol isn’t glamorous, and no one looks forward to its part in research. Yet, every risky encounter offers a reminder — personal protection, strong ventilation, and fast spill response pay off. Good habits turn into safety culture. That’s a better result than any shortcut, every single time.
Pungent, Persistent, and Misunderstood
Anyone who’s spent time in a lab or manufacturing plant probably remembers that rank, sulfur-laced smell when someone’s working with thiols. 1-Octanethiol, an oily liquid made up of carbon, hydrogen, and sulfur, gives off an odor that hangs around long after a bottle has been closed. Odor alone doesn’t always mean a chemical is dangerous, but it does make you wonder about what’s happening in the air and, eventually, inside your lungs or on your skin.
The Health Angle
Working with 1-octanethiol, safety goggles and gloves become second nature. The strong smell isn’t just a warning sign—it actually signals that the substance can irritate your respiratory tract and your eyes, much like getting a lungful of ammonia or sulfur dioxide. Prolonged exposure leaves your throat sore or nose running. If some lands on bare hands, irritation or redness is pretty likely, too.
What about long-term effects? Animal studies have suggested some thiols, when inhaled over time, can impact the liver and kidneys. It’s true that no one’s sounding alarm bells over 1-octanethiol in the same way as with mercury or benzene, but the data isn’t robust. There’s also the risk of accidents—spills or leaks in a busy workspace could lead to higher-than-normal exposure without the right ventilation.
Familiar rules about chemical safety always apply: good ventilation, fume hoods, and regular checks of storage containers. Safety Data Sheets flag 1-octanethiol for potential harm, and anyone who spends time near it should pay attention to respiratory protection and avoid direct skin contact.
Where the Environment Comes In
1-Octanethiol doesn’t just stop at hurting your nose: if it escapes into the environment, the story keeps unfolding. Chemical spills don’t stay put. Water runoff can bring this compound straight into soil and waterways. Nature doesn’t have much patience for organic sulfur compounds—thiyl groups break down slowly, which means soil and groundwater can get contaminated.
Small aquatic organisms can pick this up, sometimes leading to toxic effects at relatively low concentrations. Studies on similar sulfur-organic compounds paint a picture of fish kills and dying insects. If that chain reaction starts, bigger animals eating contaminated insects or plants start to feel the effects, too.
Air pollution is another piece. Volatile organic compounds react in sunlight and turn into smog or toxic byproducts. Even if 1-octanethiol seems minor compared to gasoline or industrial solvents, every bit adds to the problem, especially near manufacturing sites.
Solutions and Real-World Responsibility
Addressing these risks goes beyond putting up warning signs. Chemical plants and labs must treat 1-octanethiol spills quickly and store it in tightly-sealed containers in well-ventilated rooms. On a bigger scale, manufacturers should look for alternatives or design procedures that trap and neutralize fumes, cutting down on emissions at the source.
Training workers makes a real difference, too. Anyone handling chemicals should know about protective gear and emergency wash stations—not just where they are, but how to use them when seconds count. A culture that prizes routine monitoring over cost-cutting will keep both people and wildlife out of harm’s way.
Real safety comes from mixing good science with attention to detail: reading data, trusting your nose, and cleaning up before a mistake spreads beyond the lab walls. 1-octanethiol isn’t a household name, but the story it tells is the same old lesson. Respect chemicals, watch the environment, and never ignore a warning sign—even if it’s just a powerful stink.
| Names | |
| Preferred IUPAC name | octane-1-thiol |
| Other names |
Octyl mercaptan
n-Octyl mercaptan n-Octanethiol 1-Mercaptooctane |
| Pronunciation | /ˈoʊk.teɪn.θaɪ.ɒl/ |
| Identifiers | |
| CAS Number | 111-88-6 |
| Beilstein Reference | 1209240 |
| ChEBI | CHEBI:38789 |
| ChEMBL | CHEMBL51593 |
| ChemSpider | 85996 |
| DrugBank | DB02243 |
| ECHA InfoCard | 100.004.550 |
| EC Number | 203-928-6 |
| Gmelin Reference | 82748 |
| KEGG | C01642 |
| MeSH | D008104 |
| PubChem CID | 8125 |
| RTECS number | RG3675000 |
| UNII | K1P7D9M39E |
| UN number | UN 3332 |
| Properties | |
| Chemical formula | C8H18S |
| Molar mass | 146.28 g/mol |
| Appearance | Colorless to yellow liquid |
| Odor | Unpleasant strong mercaptan |
| Density | D=0.842 g/mL at 25 °C(lit.) |
| Solubility in water | Insoluble |
| log P | 4.39 |
| Vapor pressure | 0.07 mmHg (25°C) |
| Acidity (pKa) | 10.5 |
| Basicity (pKb) | pKb = 3.47 |
| Magnetic susceptibility (χ) | -68.0×10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.436 |
| Viscosity | 3.82 mPa·s (20°C) |
| Dipole moment | 1.66 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 395.7 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -222.2 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -5110.7 kJ/mol |
| Hazards | |
| GHS labelling | GHS02, GHS07, GHS08 |
| Pictograms | GHS07,GHS08,GHS09 |
| Signal word | Warning |
| Hazard statements | H226, H302, H311, H315, H317, H331, H400, H410 |
| Precautionary statements | P210, P233, P240, P241, P242, P243, P261, P273, P280, P303+P361+P353, P305+P351+P338, P337+P313, P370+P378, P403+P235, P501 |
| NFPA 704 (fire diamond) | 2-2-0-HS |
| Flash point | 74 °C (closed cup) |
| Autoignition temperature | 215 °C |
| Explosive limits | 1.1% – 6.0% |
| Lethal dose or concentration | LD50 (oral, rat): 820 mg/kg |
| LD50 (median dose) | LD50 (median dose): Oral rat LD50 = 1,290 mg/kg |
| NIOSH | TI0700000 |
| PEL (Permissible) | PEL: 0.5 ppm (skin) |
| REL (Recommended) | 2 ppm |
| IDLH (Immediate danger) | 500 ppm |
| Related compounds | |
| Related compounds |
1-Butanethiol
1-Pentanethiol 1-Hexanethiol 1-Heptanethiol 1-Nonanethiol 1-Decanethiol |