Methyl 2-Bromooctanoate: A Deep Dive into Synthesis, Safety, and Future Prospects

Historical Development

Methyl 2-bromooctanoate has an interesting backstory rooted in the search for better intermediates in pharmaceutical and materials research. Chemists from the latter half of the 20th century pushed hard to expand the toolkit for manipulating carbon chains, especially those that could serve as functional platforms for making more intricate molecules. As halogenated esters gained traction, the community found that brominated analogs like methyl 2-bromooctanoate brought reliability and selective reactivity to the table. Organic laboratories, large and small, started including this compound in their standard set of building blocks, with patents for its use in custom syntheses showing up steadily from the 1970s onward. Its journey says a lot about how small tweaks to a molecule—a methyl group, a bromine at the second carbon—can open new doors in organic chemistry.

Product Overview

In the lab, methyl 2-bromooctanoate often comes across as a pale, oily liquid. Its value largely depends on the role it plays in other syntheses—rarely does it appear in the final formulation of pharmaceuticals or advanced materials. The molecule’s structure—a C8 aliphatic chain carrying a bromine atom at the 2-position and topped with a methyl ester—gives it a reactivity profile prized by synthetic chemists. I’ve worked with similar β-bromo esters, and the ease of transforming these into diverse carbon skeletons makes them an everyday staple for advanced organic work. While some suppliers target academic researchers, others tailor the product toward contract manufacturers who need both scale and purity.

Physical & Chemical Properties

Looking at its structure, methyl 2-bromooctanoate clocks in at a molecular weight north of 253 g/mol. At room temperature, it behaves as a clear to slightly yellowish oil, with a faint, sometimes sweet odor—as is typical of many mid-chain esters. Its boiling point hovers in the 240–260°C range, but volatility isn’t a major concern at ambient conditions, since that long aliphatic tail keeps things grounded. The presence of the bromine atom at C2 means greater reactivity than the parent octanoate, especially in nucleophilic substitution or elimination reactions. These properties aren’t just trivia—they shape every aspect of its storage and handling, as even small exposure to moisture can risk slow hydrolysis or decomposition.

Technical Specifications & Labeling

Anyone buying methyl 2-bromooctanoate from a reputable supplier pays close attention to purity certificates. Reputable batches usually report excess of 98% purity, with water content typically under 0.5% and a well-documented breakdown of minor byproducts, which may include unreacted octanoic acid or trace halogenated impurities. Labels follow standard chemical safety conventions, with hazard pictograms for skin and eye irritation. You can count on clear batch numbers—crucial when tracing any unexpected reaction outcome or process hiccup.

Preparation Method

Many organic chemists, myself included, have made methyl 2-bromooctanoate by starting with octanoic acid. Esterification turns it into methyl octanoate before a carefully controlled bromination targets the alpha-position. The go-to method relies on using N-bromosuccinimide (NBS) under light or a radical initiator. This approach delivers high selectivity for the second carbon, thanks to the electron-withdrawing kick from the ester. I’ve seen improvements through the use of phase-transfer catalysts, which speed up bromine transfer at milder temperatures, helping to preserve yield and reduce byproduct formation. Reaction workups matter—a proper aqueous quench, efficient extraction, and gentle purification over silica get you a product clean enough for most applications.

Chemical Reactions & Modifications

Methyl 2-bromooctanoate serves as a platform for all sorts of modifications. The most useful trick up its sleeve is the bromine at C2, which welcomes substitution by nucleophiles—a process essential for making amino acids, alcohols, nitriles, or more elaborate frameworks. In my experience, this intermediate participates cleanly in displacement with alkoxides or amines, which chemists use to dial up molecular complexity. It also responds well to organometallic reagents, providing access to chain-extended products through cross-coupling reactions. The versatility grows when you deprotect or hydrolyze the ester position, which lets you feed these derivatives straight into new synthetic routes.

Synonyms & Product Names

Methyl 2-bromooctanoate hides behind a few alternate names in catalogs and literature. You’ll see it referred to as methyl α-bromooctanoate, methyl 2-bromo-caprylate, or just 2-bromooctanoic acid methyl ester. In chemical registries, you’ll come across unique identifiers for regulatory or trade purposes. Regardless of the name, its core applications track back to the qualities brought by the β-bromo ester group.

Safety & Operational Standards

Labs and pilot plants treat methyl 2-bromooctanoate as a moderate hazard. Like many small halogenated compounds, it poses a risk to skin and eyes—direct contact burns, and inhalation stings the respiratory tract. Personal protective gear, including gloves and splash goggles, becomes routine. My policy always involved dedicated spill kits and good fume hoods, a practice drilled in by stories of minor spills that developed into much larger cleanups. Waste disposal regulations set strict protocols; brominated organic compounds don’t belong down the drain and call for professional hazardous waste collection. Continuous training, up-to-date MSDS sheets, and regular safety drills underpin every successful operation involving this substance.

Application Area

Most methyl 2-bromooctanoate ends up as a stepping stone in making new organics. One of its key uses lands in pharmaceutical R&D, especially during the push to craft unusual amino acid analogs or chain-elongated building blocks for drug candidates. Some specialty polymer sectors pick it up for making functionalized materials, though you won’t see it on the scale of commodity plastics. I’ve watched as fine chemicals and flavor compound developers leverage its pattern—halogenated, easily substitutable esters make clever starting points for tailored molecules. Researchers interested in new surfactants, agrochemical leads, or advanced lubricants keep an eye on intermediates like this to cut time off development cycles.

Research & Development

Innovation with methyl 2-bromooctanoate tracks advances in green chemistry and synthesis routes. Efforts lean toward better atom economy, less toxic solvents, and real-time reaction monitoring. Chemists are diving into continuous-flow systems to improve yields and trim waste—a move mirrored in my own experience swapping hazardous batch processes for streamlined microreactor runs. Companies also invest in finding biocatalytic approaches to bromination that could sidestep wasteful chemical initiators. Academic groups keep pouring into this area, publishing new synthetic mutations and exploring broader substrate scopes, widening the compound’s reach across research frontiers.

Toxicity Research

Toxicology studies show methyl 2-bromooctanoate demands respect. Acute exposure has been shown to irritate eyes and skin, while animal models suggest certain brominated esters, through metabolism, can generate toxic byproducts that may affect the liver and kidneys. Occupational exposure limits stay low, and I’ve seen strict rules around air quality and emergency wash stations in any facility that handles liter-plus quantities. The push for substitution and safe handling comes straight from these studies. Regulatory bodies in Europe and North America track its use, keeping the pressure on manufacturers and end-users to document and minimize exposure.

Future Prospects

Demand for intermediates like methyl 2-bromooctanoate hinges on new areas of discovery chemistry and the drive to build more sustainable, selective syntheses. Researchers remain focused on uncovering bio-based alternatives for feedstocks and greener routes for halogenation. Methyl 2-bromooctanoate serves as both a benchmark and a testbed for new process improvements, including waste reduction and energy efficiency in manufacturing. Looking ahead, improved regulatory guidance and safer production methods could open more niches, especially in pharmaceutical innovation and specialty materials—provided the industry keeps pace with sustainability and safety expectations. The story of methyl 2-bromooctanoate echoes a wider trend: progress in chemistry depends as much on mastering known reagents as inventing entirely new ones. That’s why the sharp focus on efficiency, safety, and environmental impact continues to shape its future.



What is the chemical formula of Methyl 2-Bromooctanoate?

Understanding the Basics

Over the years, plenty of people have asked why the chemical formula of certain compounds matters. Take Methyl 2-Bromooctanoate. Its chemical formula is C9H17BrO2. This simple string of letters and numbers gives away everything a chemist, pharmacist, or researcher needs before even getting close to a beaker. Knowing that methyl part signals an ester, the bromine on the second carbon changes how this molecule interacts with other materials. The octanoate tells us it stems from an eight-carbon chain, a key building block in many applications.

Why Details Like These Matter

No one gets excited seeing C9H17BrO2 on a label, but those 11 characters set boundaries. In drug development, a small shift—like swapping where the bromine lands—can flip how a compound acts in the body. Get the formula wrong, and the entire reaction or experiment fails. In my time as a technician in a small lab, I saw the headaches that pop up when colleagues made assumptions. We wasted days because two methyl esters with similar names had entirely different formulas; one contained iodine instead of bromine. Results looked odd, and some repeat runs got scrapped. Methyl 2-Bromooctanoate, with its unique structure, serves as a cornerstone in chemical synthesis, especially for building more complex molecules that end up in medicines or specialty materials.

Safety and Handling: Facts Over Convenience

Laboratory safety relies on knowing exactly which compound is on hand. Brominated chemicals, like this one, carry their own set of hazards. Bromine can cause skin burns and its fumes irritate the lungs. Mixing up formulas isn’t just a matter of ruined experiments; it risks health and maybe life. Chemical formulas aren’t just details for paperwork. They guide which personal protective equipment to suit up with and whether extra ventilation is needed for the workspace. A 2016 study published by the American Chemical Society highlighted that more than a quarter of lab accidents trace back to confusion about labeling or chemical identification. With Methyl 2-Bromooctanoate, a clear label stating C9H17BrO2 eliminates guesswork. It helps ensure that no matter who walks into the lab, everyone’s reading the same facts.

Value for Researchers and Innovators

People outside the chemistry world might glance past those symbols without a thought, but those formulas drive every decision in a synthetic process. Methyl 2-Bromooctanoate’s formula lays out a map for what reactions are possible. Chemists use it to figure out what might happen if they bring in other reagents or to check compatibility in a larger pathway. The presence of a bromine atom brings reactivity at specific spots in the chain, which often gets leveraged in pharmaceutical research or materials engineering.

Looking Ahead: Education and Diligence

Every new scientist should get used to double-checking formulas before anything else. Modern computer systems help, but human habits of careful verification matter most. During training, I watched mentors check not just formulas but physical features—odor, color, viscosity—so that no step got overlooked. Institutional protocols encourage triple-checking not because folks enjoy paperwork, but because every letter in C9H17BrO2 counts. Respecting this attention to detail keeps innovation safe and on track. Methyl 2-Bromooctanoate stands as one more reminder that accuracy lives at the core of good science.

What are the main applications or uses of Methyl 2-Bromooctanoate?

Getting to Know Methyl 2-Bromooctanoate

Methyl 2-bromooctanoate sits on the shelf as a clear, pale liquid, but its reach stretches much further than a single container. In labs, this compound shows up whenever chemists work with long-chain structures. For anyone who's spent time in a synthetic organic chemistry group, spotting a bottle of methyl 2-bromooctanoate means you’re near a team building molecules for pharmaceuticals, new materials, or pesticides. As anyone working in chemical development can tell you, this sort of reactant helps bridge the gap between raw ingredients and something useful in the real world.

Key Role as a Building Block

The chemical’s main job is as a starting material. Methyl 2-bromooctanoate brings an eight-carbon chain with a bromine atom waiting to react. That bromine’s reactivity opens doors—swap it for another group, couple it with something else, or stretch the chain even longer. In practice, many research projects wouldn’t leave the ground without access to building blocks like this. My own experience in a university synthesis lab taught me that finding the right precursor can save weeks of frustration. With methyl 2-bromooctanoate, you get a shortcut for building more complex molecules.

Pharmaceutical and Agrochemical Synthesis

The labs behind many medicines and crop-protection products lean heavily on simple but reliable molecules. Developing new active ingredients often requires constructing carbon skeletons, tweaking their shapes, or adding a twist by introducing halogen atoms for new biological activity. Methyl 2-bromooctanoate steps in as a favored candidate for these sorts of reactions. Various scientific journals and patent filings show its fingerprints on molecules tested as enzyme inhibitors, anti-inflammatory drug candidates, or experimental insecticides.

One reason methyl 2-bromooctanoate stays popular involves its balancing act: the chain is long enough to mimic fatty acids, yet the bromine allows for advanced customization. Chemists exploit this by reacting it with a wide range of nucleophiles or by swapping the bromine in cross-coupling reactions. For instance, a study cited in the Journal of Medicinal Chemistry outlined pathways for making long-chain amines—core units in antiviral drugs—starting with methyl 2-bromooctanoate.

Specialty and Material Chemistry

Beyond the labs dreaming up new drugs, this molecule finds fans across specialty chemical manufacturing. Polymers sometimes get their start from brominated intermediates. Surfactant developers rely on methyl 2-bromooctanoate to add hydrophobic tails or custom chains with specific functions. My stint at a small materials startup gave me a close look at how a molecule like this could form the backbone of an entirely new plasticizer, with testing that ran from bench scale all the way up to product launch.

The fine chemicals shop floors also tell another story about its use. Catalogs list methyl 2-bromooctanoate as a go-to for constructing flavor and fragrance ingredients, which demand both creative chemistry and strict control over purity. The reproducibility and versatility drive its continued listing in every major chemical supplier’s inventory.

Meeting Safety and Environmental Expectations

As more companies face scrutiny over chemical safety, handling hazardous brominated intermediates raises concerns. Research groups now look for greener alternatives or improved waste management for by-products. I’ve seen stronger push lately for tighter storage control, better ventilation, and improved training for new lab members dealing with potent reagents like this ester. Transparency about sourcing, disposal plans, and potential exposure risks matters more than ever, helping both regulators and downstream users feel confident.

Pushing Forward: Where Research and Practice Converge

Methyl 2-bromooctanoate stands as more than a mere reagent: its role reflects modern chemistry’s drive for both efficiency and customization. From blockbuster drugs to proprietary polymers, this compound pulls its weight, reminding many in the field that today’s routine substances often sit behind tomorrow’s breakthroughs. As the industry keeps raising the bar for both performance and responsibility, the choices around such building blocks—from sourcing to waste management—will shape the future just as much as the science itself.

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

Why Care About Safe Storage?

People who work with chemicals like Methyl 2-Bromooctanoate know dangers aren’t always obvious. This isn't your everyday household product. It’s a specialty chemical, often used for research, synthesis, or in pharmaceutical labs. Taking chances with safety or ignoring proper storage practises can lead to serious health risks, property loss, or cross-contamination—issues I have seen firsthand in shared lab spaces. Careless mistakes put entire projects and people at risk.

What’s So Tricky About This Compound?

Methyl 2-Bromooctanoate is a clear, colorless to pale yellow liquid, but its outward simplicity hides chemical quirks. It reacts quickly with bases and acids. Spilled on skin, it can cause irritation, maybe even burns. A bit of vapour in the air and indoor air quality drops quickly—respiratory discomfort catches some people off guard. The rules for storing this compound always matter because its risks aren’t limited to the container.

Key Storage Rules

Keep this chemical in tightly closed glass bottles—polyethylene or polypropylene sometimes degrade. The bottle goes on a designated shelf, preferably in a chemical storage cabinet away from heat, sparks, or any source that could cause ignition. One mistake I often see: storing volatile chemicals in open shelving or close to windows. Sunlight speeds up breakdown and can make vapors seep out.

Never keep bottles above eye level. I’ve seen splashes from dropped bottles and the results are never pretty. Temperature control does a lot to keep Methyl 2-Bromooctanoate stable. Always choose a cool, dry space. Some suggest refrigeration, but for short-term storage, a well-ventilated, dry cabinet works well—as long as the temperature stays steady, ideally below 25°C (77°F). Humidity and temperature changes can stress containers, causing leaks.

Safe Handling Practices

Personal experience says gloves, safety goggles, and a lab coat aren’t overkill—they’re the minimum. Spills sting. Disposable gloves like nitrile work best, but never trust one glove for everything. Consider a face shield or fume hood during transfers. I’ve learned to double-check that fume hoods are working by looking for steady airflow, not just assuming the system is running.

Never pipette by mouth. Use manual or electronic pipettors. Clean pipetting equipment after every use to avoid contaminating other chemicals. Even a drop or two can trigger unwanted reactions. Label bottles with date and full name of chemical, including hazard warnings—generic “brominated ester” labels help no one in an emergency.

Dealing with Waste and Emergencies

All waste must go in a pre-labeled, tightly sealed hazardous waste container set aside for halogenated organics. In case of a spill, sand or commercial absorbent granules catch liquid fast. Never use paper towels, since it spreads contamination and can lead to dangerous decomposition. If the spill is large or on skin, get help right away. Wash exposed skin with cold running water, remove contaminated clothing, and let your safety officer know.

Why Follow These Steps?

I’ve watched labs grind to a halt after one careless storage mistake. It's humbling to see a whole bench of research end up in an emergency room or biohazard bag. Smart habits and thoughtful preparation protect more than your own work area—they keep the whole team on track. The science always goes better with that peace of mind.

Is Methyl 2-Bromooctanoate hazardous, and what safety precautions should be taken?

What Kind of Chemical is Methyl 2-Bromooctanoate?

Methyl 2-Bromooctanoate shows up in labs and chemical plants with some regularity, often showing up as a clear or yellowish liquid. The structure puts it in the family of alkyl bromides, a group known for being more hazardous than most folks realize. Handling it without respect for its capabilities can lead to trouble no scientist or technician wants to deal with.

Risks of Exposure

A lot of chemical compounds hide their dangers, and this one fits that mold. Skin contact or inhalation of vapors brings significant risk. Brominated chemicals often cause skin and eye irritation, sometimes more severe reactions, and even breathing in a small amount of vapor or mist can irritate the respiratory tract. Those cases of redness, watery eyes, or persistent cough? Lab workers have learned it’s smarter to stay ahead of them than try to treat them after the fact. Chronic exposure brings a new set of problems, including organ damage over a long haul. The American Conference of Governmental Industrial Hygienists (ACGIH) and similar bodies have flagged enough bromine compounds for health effects that nobody should get complacent around this stuff.

Methyl 2-Bromooctanoate also combines flammability risk with toxicity. Spills or splashes near ignition sources create hazards beyond the chemical burns and poisoning. Inhaled vapors can travel, so being in the next room doesn’t guarantee safety if ventilation lacks punch. That’s where most safety slip-ups happen—by underestimating a chemical’s ability to spread trouble fast.

Protective Practices for Handling

Gloves, goggles, lab coats, and a properly functioning fume hood do more than tick boxes during lab inspections. Nitrile gloves work best; latex lets too much slip through. My experience shows most folks reach for goggles, but a face shield adds another layer for those who regularly transfer or pour. Fume hoods need airflow tested every few months, not just once a year. Filters in those hoods clog up with heavy use, bumping exposure back up to risky levels. So many illnesses start when people ignore that little sticker saying “Last checked six months ago.”

Storing methyl 2-Bromooctanoate presents another challenge. No sunlight, low moisture, away from acids and strong bases—it’s not optional. Some chemists keep it under inert gas to handle decomposition or unwanted reactions. Chemical compatibility charts become daily reading if you want to avoid cross-reactions that can turn a simple bottle into a gas hazard. Never store beside common solvents like acetone or alcohol; in emergencies, those combinations lead to headaches or worse.

Emergency Response and Waste Disposal

I’ve seen what happens when cleanup crews try to neutralize chemical spills without knowing the compound’s behavior. Spills demand more than paper towels. Absorbent materials, full protective clothing, and readiness with an eyewash or safety shower prove themselves whenever a bottle tips. That’s not an overreaction—it’s the voice of hard-earned experience. Local and federal regulations dictate how to dispose of this material; anyone dumping it down the drain risks not just their job but the community’s well-being. Professional waste disposal costs money, but it saves far more than it spends.

Building Safety Culture in the Workplace

Some labs rely on posters and binders, but nothing replaces hands-on training and honest discussion. Supervisors and experienced staff owe it to everyone to share cautionary tales and near-misses. Institutions with regular drills and open communication seasons see fewer accidents and less severe outcomes. Respecting chemicals isn’t paranoia—it’s what separates safe labs from stories in the news.

What is the typical purity or assay of commercially available Methyl 2-Bromooctanoate?

Looking at Purity for an Everyday Chemical

Folks who handle organic chemicals probably bump into methyl 2-bromooctanoate sooner or later. This molecule plays a part in making specialty compounds, flavor modifiers, and sometimes pharmaceutical building blocks. Those little numbers for purity—called assay—aren’t trivial details. A chemist’s plans can go south fast with a batch full of extra junk. So, what’s the real deal with methyl 2-bromooctanoate purity in practice?

Packing a Punch: What Purity Levels Mean in Real Labs

Most chemical suppliers, big or small, list methyl 2-bromooctanoate with assay values clustered between 97% and 99%. Those last wiggles—toward 99%—can matter more than most non-chemists imagine. A “97% pure” bottle looks clear and fine to the eye, but ask someone running a sensitive synthetic route: that last two percent of contaminants can clog up reactions or muddy up NMR readings, which wastes time and money. Sigma-Aldrich, TCI, and Alfa Aesar, leaders in the field, all offer methyl 2-bromooctanoate in this range, typically guaranteeing purity with gas chromatography.

Why Does It Never Hit 100%?

Absolute purity is a chimera in the bulk chemical world. Organic synthesis leaves behind byproducts, left-over solvent, and sometimes trace water. The manufacturer can use distillation, recrystallization, and column chromatography—but every step raises the price and lengthens delivery time. Most demand for methyl 2-bromooctanoate lives in labs making grams, not tons, so the industry stops short of pharmaceutical-grade purification. Would I pay double or triple for that extra half percent? Not unless my project really called for squeaky cleanliness.

What’s at Stake for Researchers?

If you work in a university lab, you learn quickly that assay isn’t just an abstract number. At 97%, you expect a little trouble—unexpected peaks in GC spectra, off smells, or oily residue after solvent removal. These clues force you to troubleshoot, burning through both sample and graduate student patience. At 99%, things turn smoother: fewer failed reactions, tighter data, and reactions that behave by the book. The science just feels better.

Fact-Checking and Supplier Trust

Quality often traces back to documentation. Reliable suppliers provide not just a number but chromatograms, certificates of analysis, and clear batch tracking. I pay attention to this paperwork because corners get cut when prices get squeezed. One year, a batch from a budget brand ruined a week’s work. Now, I spend a few minutes with the supplier’s PDFs before ordering. The lesson sticks: purity on paper means less stress at the bench.

Moving the Needle: Solutions and Progress

Labs feeling the pinch of less-than-ideal purity can take matters into their own hands. A quick distillation or passing the compound through a short silica column can boost purity into the “high 90s” for most uses. Major institutions are getting better about batch-testing their chemicals, then sharing results internally. This community-based vetting keeps everyone sharper—and suppliers on their toes.

Bottom Line for Scientists

A typical methyl 2-bromooctanoate batch lands between 97% and 99% pure. The space between those numbers can mean failed syntheses or smooth success. No chemist wants to rerun reactions just because of a shortcut in the supply chain. Checking paperwork, spending a bit more for trusted brands, and adding a purification step when necessary takes the sting out of those last few impurities. That’s worth more than a passing glance at an assay percentage.

Methyl 2-Bromooctanoate
Methyl 2-Bromooctanoate
Methyl 2-Bromooctanoate
Names
Preferred IUPAC name Methyl 2-bromooctanoate
Other names Methyl 2-bromooctanoate
2-Bromooctanoic acid methyl ester
Methyl 2-bromo-octanoate
Pronunciation /ˈmɛθɪl tuː ˌbroʊmoʊˈɒktəˌneɪt/
Identifiers
CAS Number 18336-24-2
3D model (JSmol) `C[C@@H](CCCCCCBr)C(=O)OC`
Beilstein Reference 1309286
ChEBI CHEBI:131599
ChEMBL CHEMBL2236723
ChemSpider 14849583
DrugBank DB08308
ECHA InfoCard 100_108_4
EC Number 613-610-0
Gmelin Reference 77493
KEGG C19207
MeSH Chemical Phenomena", "Esters", "Methyl Compounds", "Bromides", "Octanoic Acids
PubChem CID 12362667
RTECS number NL5954000
UNII 45B8C8F9GU
UN number UN2735
CompTox Dashboard (EPA) DTXSID2050433
Properties
Chemical formula C9H17BrO2
Molar mass 251.13 g/mol
Appearance Colorless to pale yellow liquid
Odor sweet
Density 1.183 g/mL
Solubility in water Insoluble
log P 3.7
Acidity (pKa) pKa ≈ 25
Magnetic susceptibility (χ) -63.17e-6 cm³/mol
Refractive index (nD) 1.457
Viscosity 45 cP (20 °C)
Dipole moment 2.20 D
Thermochemistry
Std molar entropy (S⦵298) 527.7 J·mol⁻¹·K⁻¹
Std enthalpy of formation (ΔfH⦵298) -460.7 kJ/mol
Std enthalpy of combustion (ΔcH⦵298) -1562.4 kJ/mol
Pharmacology
ATC code Not assigned
Hazards
Main hazards Harmful if swallowed. Causes skin irritation. Causes serious eye irritation. May cause respiratory irritation.
GHS labelling GHS02, GHS07
Pictograms GHS05,GHS07
Signal word Warning
Hazard statements H302, H315, H319, H335
Precautionary statements P261, P280, P305+P351+P338, P304+P340, P312
Flash point 97.3 °C
LD50 (median dose) LD50 (median dose): 2400 mg/kg (rat, oral)
NIOSH BJ8400000
PEL (Permissible) Not established
REL (Recommended) 50 mg
IDLH (Immediate danger) Not established
Related compounds
Related compounds Methyl octanoate
2-Bromooctanoic acid
Ethyl 2-bromooctanoate
2-Bromononanoic acid
Methyl 2-chlorooctanoate
Methyl 2-bromodecanoate