Dimethylpropylamine didn’t show up by accident. Long before sophisticated synthesis methods came along, chemists learned to manipulate amines because they could be built into all kinds of useful molecules. Tracking its origins, this compound popped up in research somewhere between the spread of basic amine chemistry in the early 1900s and the post-war boom in industrial organic production. Lab notes from these decades show teams experimenting with secondary and tertiary amines to replace older, less stable chemicals in everything from insecticides to solvents. The spotlight on tertiary amines like dimethylpropylamine came from this push for more targeted, resilient building blocks—and you’ll still find traces of that drive today, especially when manufacturers look to improve process safety or reduce downstream environmental risks. Early patents from industries trying to carve out cheaper, more controllable syntheses helped tie together what we know about the compound’s usefulness, and later studies introduced analytical standards for purity, vapor pressure, and toxicology, setting the foundation for today’s research.
Dimethylpropylamine pops up most often as a colorless liquid with a recognizable fishy odor. Because it’s a tertiary amine, it packs both chemical muscle and versatility, lending itself to roles as an intermediate in synthesis, pH adjustment, and surface treatment. Chemical plants and research labs favor it because it blends solubility in water and organics, doesn’t corrode equipment like harsher amines, and stands up under heat—crucial where reaction margins run tight. Users watch its physical performance, such as its boiling range, vapor behavior, and environmental escape risk, before rolling it out to any large-scale process. It becomes the backbone for resolving charges in the resin and paint world, unlocking more stable dispersions for coatings that last through real-world abuse.
Dimethylpropylamine isn’t just another amine on the shelf. It usually appears as a clear, mobile liquid at room temperature. Its molecular formula, C5H13N, and a molar mass that lands near 87.16 g/mol, keep it light enough for efficient vapor handling but dense enough to avoid flammability headaches some lighter amines bring. Its boiling point sits around 83–85°C, and its melting point drops far below freezing, which means plant engineers don’t need to worry much about storage in typical climates. Log octanol-water partition coefficients hover close to zero, marking middle-of-the-road environmental transport. The nitrogen atom brings in basicity, landing with a pKa of roughly 10.7, letting it grab protons in acid-buffering jobs. Vapor pressure and miscibility levels remain high, so keeping containers sealed and handling under ventilated hoods is standard, especially if the working spaces don’t like odors lingering.
Producers of dimethylpropylamine publish specs that leave little room for guessing. Typical industrial grades call for purity above 98%, ideally with water content less than 0.5% by mass. Color numbers from standard ASTM scales keep out product that might have oxidized during transit. Safety data sheets and container labels print hazard warnings in bold, listing its strong, characteristic odor, potential for eye and skin irritation, and strong recommendation for goggles and gloves in open-air work. Material identifiers, such as CAS number 926-24-1 and UN/NA transport codes, match up with local regulations, keeping supply chain managers and compliance officers in sync. Lot numbers, batch records, and expiry dates stay tied to every drum, since product recalls and downstream tracking weigh increasingly heavy in risk management plans.
To cook up dimethylpropylamine, chemical plants favor alkylation routes—turning out this tertiary amine in reactors charged with dimethylamine and n-propyl halide. Operators run the reaction under pressure in the presence of an organic solvent, throwing in a base like sodium carbonate to catch any stray acids. Post-reaction phases start simple: distillation pulls off the product, leaving behind inorganic salts and by-products. Manufacturers often run secondary purification, such as fractional distillation, if purity targets run higher for pharmaceuticals or electronics. Some plants lean toward catalytic hydrogenation of precursor nitriles, if feedstock economics favor it, but safety plays big—each path gets stress-tested for unwanted side reactions or by-product formation, especially quaternary ammonium salts that mess with downstream specs.
Working with dimethylpropylamine unlocks reaction options. In organic synthesis, it walks into nucleophilic substitution and alkylation jobs, slotting into side chains or building blocks for dyes, agrochemicals, or pharma intermediates. It binds up acids or runs buffer duty in protocols that demand narrow pH control. Labs tap its willingness to be quaternized—reacting with alkyl halides or sulfates to build quaternary ammonium salts, which then hold value in the surfactant or disinfectant trade. Its lone pair sits ready for acylation, working as a partner in peptide synthesis or in the tailoring of advanced polymers. Chemists keep protocols tight, since tertiary amines can oxidize to amine oxides or nitrosamines under imprecise conditions—a major headache in any regulated pipeline.
The world of chemistry rarely sticks to one name. Dimethylpropylamine goes by plenty of aliases and trade names, popping up as N,N-Dimethyl-1-propanamine, 1-Propanamine, N,N-dimethyl-, and sometimes just DMPrA. Lists from global registry databases also include its CAS number, 926-24-1, and EPA identifiers for environmental reporting. Bulk suppliers and catalog houses prefer clear labeling for quick reference, especially when shipping between countries or regions with different chemical inventory rules.
People who work around dimethylpropylamine respect its risks. As a volatile, basic amine, it stings eyes, irritates skin, and releases vapor that builds up in enclosed spaces. Safety data sheets point to the need for full-face shields, nitrile gloves, and local exhaust ventilation, especially if loading or dosing takes more than a few minutes. Emergency protocols for spills call for dilute acid scrubs and quick containment; flammable limits and flash points drive rules for outdoor storage and non-sparking tools. Occupational exposure guidelines limit airborne concentrations, and workplaces lean on continuous gas monitoring in larger facilities. Transport rules under DOT and ADR assign it to hazard classes that demand decent secondary containment and clear labeling, no matter if the journey stays local or crosses borders. For chronic exposure, regulatory agencies maintain watch lists for amines in indoor air; studies on metabolic breakdown keep pressure on employers to track both worker health and environmental emissions.
Dimethylpropylamine earns its paycheck across several industries. In chemical manufacturing, it steps up as a synthesis intermediate in making agrochemicals, dye-stuffs, and performance polymers. Water treatment plants depend on its basicity for pH adjustment—especially in places where chlorine treatment runs hot and fast. Paint and coatings manufacturers use it in resin formation and as a neutralizing agent, while the world of pharmaceuticals keeps it in play for building small molecule drugs that demand a tertiary amine anchor. Specialty surfactants and antistatic agents tap into its ability to build up charge density under the right modifications. A handful of fragrance and flavor companies look to it, albeit in tightly regulated, trace quantities as part of complex blends. Waste treatment operations use it as a scrubbing agent, binding up acid gases before venting air back to the environment.
Research teams focus on more than just production scale. Universities and private labs investigate improved catalysts for cleaner synthesis routes, aiming to cut waste and run reactions at milder conditions. Environmental scientists dig into degradation pathways, mapping out how dimethylpropylamine breaks down in soil and water and flagging intermediates for closer toxicity screens. Analytical chemists refine detection methods, from headspace gas chromatography to mass spectrometry, to catch even those low-level leaks no one notices until it’s too late. Pharmaceutical groups seek new therapeutic uses, exploring structures where dimethylpropylamine’s molecular skeleton could boost bioavailability or tweak pharmacokinetics. Material engineers design hybrid polymers linking tertiary amine groups for ion-exchange membranes or transportable specialty resins.
Dimethylpropylamine tests low for acute toxicity compared to harder-hitting industrial amines, but recurring exposure can sensitize or irritate skin and mucous membranes. Studies in rats and rabbits suggest the threshold for systemic toxicity comes in quite high, yet even modest daily exposure brings cumulative risk in high-turnover plants. Chronic inhalation can impact respiratory health, so occupational health teams run frequent monitoring, not just for workers, but also for ambient emissions near fence lines. Early toxicology flagged metabolic byproducts with potential for nitrosamine formation—raising regulatory interest since those break down into carcinogenic species without enough downstream treatment or monitoring. Environmental fate research tracks its breakdown to CO2, amines, and low-weight organics, but incomplete aerobic conditions sometimes leave residues that trouble aquatic life. Calls for greener alternatives and improved degradation keep pressure on innovators shaping next-generation amines.
Growth for dimethylpropylamine hinges on more than tradition. Clean chemistry pushes drive demand for efficient, selective syntheses, preferring amines with low vapor escape and minimal by-product formation. Regulatory rules on VOCs and workplace safety keep R&D teams innovating, searching for modifications that lower both volatility and toxicity. As bio-based feedstocks spread, producers explore renewable sources for both starting materials and energy inputs. Application outlook grows promising as electronics, battery storage, and fine chemical synthesis all turn to tertiary amines with robust performance at mild reaction conditions. The push for circular manufacturing keeps a close eye on both post-use recovery and cradle-to-grave environmental impact, shaping the narrative for every plant, lab, and end user invested in cleaner, more responsible chemistry.
Walk through any industrial park, and chances are you’ll find a place relying on dimethylpropylamine. In my early encounters as a chemical plant visitor, I caught the sharp, unmistakable scent even before checking a batch’s paperwork. Anyone spending time in basic chemical production learns quickly that dimethylpropylamine, or DMPA, gets everywhere—from plastics to refineries, from pharmaceuticals to even the surfactants in cleaners.
DMPA stands out as a powerful intermediate. It slots into processes that put food on shelves, run cars, and keep tap water drinkable. Production of agricultural chemicals often draws on this compound. That high-yield wheat or the soybeans in our groceries? Someone probably used a DMPA-based herbicide or pesticide somewhere along the way. Farm output in the modern world often calls for chemicals that can break down weeds without grinding up profits. Here’s where DMPA steps in, forming the backbone of active agents because its basic chemical structure tweaks well for resistance or stability.
Anyone working on coatings or paints has likely brushed up against DMPA. Polyurethane foams, industrial masses, and certain varnishes wouldn’t form as easily without it. In the shop, DMPA helps put the bounce in floors and car seats. Furniture production lines reach for it to improve flexibility and overall texture—something shoppers notice as soon as they sit down.
Beyond big industries, dimethylpropylamine hides in products average folks never think about. Asphalt plants use it to improve the stick and behavior of road surfacing. Oil refineries add small doses to keep machinery humming smoothly. Even the paper industry leans on DMPA in specialty treatments to boost strength so everything from newspapers to packaging stays reliable.
I watched wastewater engineers dosing DMPA-based chemicals to break up stubborn substances clogging treatment plants. Safe drinking water depends on science to clear out the tough stuff. Dimethylpropylamine becomes part of blends that speed up these purification steps. It’s not glamorous work, but my appreciation for the chemistry behind clean water only grew after seeing these applications firsthand.
Any discussion on industrial chemicals leads to hard questions about safety. Dimethylpropylamine doesn’t belong anywhere near skin, eyes, or lungs without precautions. Studies show inhalation or accidental splashes can cause burns, breathing trouble, and headaches. I know plant operators who carry respirators as faithfully as their lunches. To play it safe, companies set up perimeter monitors for leaks and rely on strict personal protection standards.
Regulatory agencies regularly review new health data on DMPA. The Environmental Protection Agency—alongside similar groups outside the US—pushes for safer handling and transparent labelling. Workers learn quickly to treat shipments with respect, not just from trusting guidelines, but by watching how seriously colleagues follow safety checklists.
Keeping an eye on safer alternatives remains a priority for anyone sitting near a processing line. Research groups search for greener, less irritating replacements by building on decades of work in organic chemistry. Yet for now, DMPA remains a staple thanks to its versatility and performance. Honest talk about risks, regular testing programs, and sound workplace policies help keep its use in check—and make sure benefits don’t come at too high a price.
Dimethylpropylamine shows up in a lot of workplaces, especially around chemical plants and manufacturing. You see it used in making rubber, dyes, and a handful of specialty chemicals. It works well in industrial processes, but it doesn’t treat skin, eyes, or lungs kindly. This chemical can give off strong vapors and cause burns. It isn’t something to take lightly. Its smell grabs your nose and lingers. Missing safety steps leaves workers open to real harm.
In my own time around industrial chemicals, nobody wanted a bare hand near this stuff. Chemical-resistant gloves top every list, and not just any gloves. Nitrile or neoprene stands up much better to leaks than plain latex. Protective goggles shield against the inevitable splashes. Full-face shields sometimes come out, especially if pouring or transferring. Working regular shifts in hot conditions, wearing long sleeves and pants, though uncomfortable, always meant fewer regrets at quitting time. Good habits like checking for rips and washing up at breaks help too. Respirators matter as well when fumes pick up in closed spaces. Fit-testing and the right cartridges make a world of difference, and a simple dust mask won’t cut it.
Poor airflow turns low-risk chemicals into a nightmare. Exhaust fans and proper hoods keep vapors in check, protecting anyone in the room. If the job takes place in a tight spot, never underestimate the benefit of opening a second exit. Local ventilation matters, catching fumes before they ever reach your breathing zone. During my first week on a plant floor, I watched a supervisor fan vapors right out of a loading bay with a few well-placed fans. That small step kept our eyes from watering and headaches to a minimum.
It never pays to trust an unmarked drum or an old bottle. Every single container, down to the smallest secondary bottle, deserves a legible label. Clear names and hazard symbols leave no room for doubt. Storage needs attention, too. Dimethylpropylamine doesn’t mix well with acids, oxidizers, or moisture. Locking it in a cool, dry area sounds like common sense, but I’ve seen plenty of folks cut corners by stuffing it into overfilled shelves. Use secondary containment, like trays, to catch leaks and avoid surprises blending underfoot or pooling into corners.
If an accident happens, panic makes everything worse. Close at hand, eyewash stations and showers must actually work — something you learn after a few surprise drills. Keeping an easy-to-find spill kit with absorbent pads and neutralizers saves precious minutes. For skin contact, flush right away with plenty of water. For a splash in the eyes, turn it into a waterfall and call for medical help. Inhaling strong vapors needs a dash outside for real, fresh air. Keeping emergency numbers taped by doors turns a close call into a lesson instead of a trip to the ER.
People remember what they practice. Clear instructions and hands-on safety training stick far better than slideshows or long-winded manuals. Workers who see their bosses wear safety gear without fail pick it up themselves. Respect grows for the process, not just the rules. In my own experience, good training kept incidents rare. Honest conversations about accidents help everyone — not to blame, but to learn. Safety isn’t just about avoiding fines. It’s about sending every worker home in the same shape, or better, than they arrived.
People throw around chemical names like confetti, but there’s something honest about understanding exactly what’s inside those names. Dimethylpropylamine doesn’t just sound technical; its formula, C5H13N, points to how even basics in chemistry can shape the world most folks don’t see. Five carbons, thirteen hydrogens, one nitrogen—for some, that’s just trivia. For others—people who work with solvents, cleaners, or pharmaceuticals—it marks out a source of power and risk, depending on how those atoms bond up and what hands they fall into.
I used to think most chemical formulas belonged on a blackboard, not in regular conversation. A few years back, a friend called me from the shop where he runs automotive maintenance. He heard the name “Dimethylpropylamine” in a product pitch and wanted to know if it would burn a hole in his workbench or his lungs. That got me curious, so I looked at its basic structure. The formula C5H13N isn’t just for science nerds—it tells workers where to hang warning signs, and guides first responders on what to grab when a drum leaks in a warehouse.
Chemicals like Dimethylpropylamine show up in labs, but they don’t stay there. Once manufacturers realize it can help make drugs, resins, or as an additive in other chemical reactions, it starts traveling. The formula C5H13N gives away enough—dimethyl groups stuck on a propylamine chain. That means this molecule is part of the larger alkyl amine family, which acts as both a backbone for synthesis and a hazard under the wrong conditions. In the hands of a chemist, this compound helps shape all kinds of products. In the hands of someone with no training, it’s a recipe for unexpected burns or worse.
I’ve seen some pretty bad chemical confusion in my time. A missed label, a wrong assumption about what goes with what, and suddenly a storage closet turns into a cleanup nightmare. Safety officers look at formulas like C5H13N and instantly think of boiling points, fire risk, and fumes. They teach newcomers to memorize formulas not because it’s tradition, but to save toes and lungs and maybe even lives. That’s not theoretical; it’s practice from repeated experience. Chemists keep formulas like C5H13N at their fingertips so they don’t mix incompatible substances or get surprised by a violent reaction on the workbench.
Better education is the biggest fix. When schools limit chemistry to filling in charts, they leave out all the real-world moments where a formula like C5H13N decides whether a day is ordinary or heads for the ER. Companies can step up, too. Clear labels, safety data sheets written so that mechanics and warehouse workers actually use them—not just scientists—end up stopping more accidents than regulations alone. Even small changes, like giving every worker a cheat sheet of common formulas they might run into, have paid off in the shops and labs I’ve visited.
Dimethylpropylamine’s chemical formula summarizes what could fill an entire textbook: risk, opportunity, the need for respect. Every formula tells a story, and in the right hands, C5H13N isn’t just a combination of elements—it’s a signal for safety, responsibility, and a chance to make routines safer for everyone down the line.
Dimethylpropylamine isn’t your everyday household item—it's a chemical with a sharp smell that can pose serious risks in careless hands. I remember my early days working in a mid-sized plant. One small spill of this stuff left our maintenance team scrambling for hours. Eyes stung, noses burned. After that, I took chemical storage a lot more seriously.
If you stack bottles of dimethylpropylamine on an open shelf, close to sunlight, you’re asking for trouble. The vapor is flammable and will catch fire from a regular spark or, worse, static electricity from a frayed cord. Heat makes those vapors build up faster, and some unlucky worker could get a faceful.
I’ve learned that a locked cabinet in a cool, ventilated room stops most disasters before they start. Local fire codes often echo this advice. Temperature tops the priorities: keep this chemical well below 40℃. Some labs use a dedicated flammable storage fridge, but plenty of industrial sites stick with a heavily vented, steel-lined cabinet with a grounding wire attached.
Any water sneaking into a dimethylpropylamine container spells corrosion and contamination. A friend at a chemical distributor once told me they lost an entire drum just because someone forgot to reseal the lid after decanting. Moisture drifted in, and within days, the product turned cloudy. Always reseal containers tightly after each use and never transfer between drums with a wet funnel.
Labels keep people out of harm’s way. Every jug and drum needs a label with the name, hazards, and emergency info. No cryptic abbreviations, legible in any light. Years ago, my colleague stored dimethylpropylamine next to an acid because he was short on space. It only takes a splash to produce toxic fumes. Always segregate this amine from acids, oxidizers, chlorinated solvents, and food prep areas. It’s more than a rule—it’s how you keep people healthy.
Limit access to those who know the material. Every year, countless warehouse workers open something unfamiliar without glove or goggle. Written training might feel tedious, but nothing beats real-life walkthroughs. I insist on hands-on sessions for new hires, showing the right gloves (nitrile or PVC), goggles, and chemical-resistant aprons. Spill kits should sit in arm’s reach, not locked in a distant cabinet.
Dimethylpropylamine burns fast. Keep stores far from ignition sources: electrical boxes, welding equipment, or open flames. Our local firefighter once drilled with us; he made us check extinguishers (class B or dry chemical) every quarter and mandated vapor alarms for bigger storage rooms. Learn the signs of a leak—smell, discoloration, or hissing. Have emergency showers and eyewash stations on the same floor, just steps from storage. Seconds matter.
Lock away what could harm. Document every transfer and disposal. Invite your local fire marshal for a walkthrough once a year and ask questions. Dimethylpropylamine will always require respect—treating it with careful storage means fewer injuries, less lost product, and a healthier team.
Dimethylpropylamine shows up in places most people never expect. Factories use it in making herbicides, pharmaceuticals, rubber, and plastics. The compound carries a sharp, ammonia-like smell, and workers handling it often wear heavy-duty gloves and respirators. That sharp odor tells its own story: here is a substance not meant for careless exposure.
Anyone who has ever met Dimethylpropylamine up close pays attention. Breathing in its fumes can irritate your nose and throat. A splash on your skin leaves a burning feeling. Hospitals have seen cases of chemical burns from this stuff, and the fluid can damage eyes in a matter of seconds. Swallowing even a little can burn the digestive tract or cause nausea, headaches, or confusion. These aren’t rare outcomes—accidental exposure still happens in many industrial workplaces.
For many chemicals, the story changes with chronic exposure. In animal studies, longer-term inhalation sometimes triggers effects on the liver or nervous system, although the research on humans remains thin. Those gaps matter. Not every workplace invests in proper ventilation or training. Workers without protective gear may face frequent headaches, sore throats, or skin rashes. Some experts suggest a potential risk for more serious health problems, but there’s no long-term data covering large groups of people. Still, any chemical that produces such immediate effects should make us pause and push for more research and tougher safeguards.
Spills can seep into soil or streams, and Dimethylpropylamine doesn’t simply vanish. Fish and aquatic life don’t have much resistance to it. The odor helps warn humans, but wildlife doesn’t have that kind of signal. Researchers have seen insect and plant communities shrivel near spill sites, and even at lower concentrations, water systems become threatened. Most water treatment plants filter out the big threats, but not every system catches small-molecule chemicals with perfect efficiency.
Airborne Dimethylpropylamine also enters the environment through evaporation during manufacturing or application. Wind might carry these tiny amounts far beyond factory gates. Local plants and crops sometimes show signs of stress after being downwind of large-scale operations. Farmers working nearby have raised complaints about eyes watering, coughs, and plants suffering odd brown patches.
Household exposure rarely happens—ordinary folks won’t find this compound sitting under the sink. For industrial users, chemical-resistant gloves, face shields, and airtight ventilation systems give real protection. Emergency teams need clear plans for spills—sand, absorbent materials, and safe disposal keep accidents from becoming disasters. Training employees to spot trouble early saves both worker health and local wildlife.
Government agencies like the Environmental Protection Agency monitor and restrict use, but self-policing carries real weight too. In my area, one chemical plant started sharing their safety procedures with nearby businesses, and everyone benefited. Community meetings and clear labels reduce confusion in case of accidents, and people who know what they’re facing react much quicker.
Living and working near manufacturing brings undeniable risks, but real oversight and upfront investment in safety cut down on accidents. Dimethylpropylamine won’t disappear from industry, so tough rules and honest conversations keep both people and nature out of harm’s way. With every accident we prevent, we learn something practical—simple steps like better ventilation and clear emergency plans tip the scales toward safety, both in the factory and out in the field.
| Names | |
| Preferred IUPAC name | N,2-dimethylpropan-1-amine |
| Other names |
N,N-Dimethyl-1-propanamine
1-Propanamine, N,N-dimethyl- Dimethyl-1-propylamine DMPrA |
| Pronunciation | /daɪˌmɛθɪlˈprəʊpɪləˌmiːn/ |
| Identifiers | |
| CAS Number | 926-41-4 |
| 3D model (JSmol) | `JSmol.loadInline("data:image/png;base64,AAAC...")` (For **Dimethylpropylamine**, the correct JSmol 3D model **string** is:) ``` CSCCN(C)C ``` *(This is the SMILES string representing the connectivity for use in JSmol or similar viewers.)* |
| Beilstein Reference | 1718736 |
| ChEBI | CHEBI:39146 |
| ChEMBL | CHEMBL48937 |
| ChemSpider | 12789 |
| DrugBank | DB11197 |
| ECHA InfoCard | 50-35-1 |
| EC Number | 203-680-9 |
| Gmelin Reference | 7926 |
| KEGG | C06565 |
| MeSH | D001178 |
| PubChem CID | 12043 |
| RTECS number | UB8050000 |
| UNII | A8L9777YF1 |
| UN number | UN2382 |
| CompTox Dashboard (EPA) | DTXSID6020282 |
| Properties | |
| Chemical formula | C5H13N |
| Molar mass | 101.19 g/mol |
| Appearance | Colorless to yellow liquid |
| Odor | Ammonia-like |
| Density | 0.7 g/mL at 25 °C (lit.) |
| Solubility in water | soluble |
| log P | 0.97 |
| Vapor pressure | 4.6 kPa (at 20 °C) |
| Acidity (pKa) | 10.73 |
| Basicity (pKb) | 3.29 |
| Magnetic susceptibility (χ) | -58.3e-6 cm³/mol |
| Refractive index (nD) | 1.393 |
| Viscosity | 0.38 mPa·s (20 °C) |
| Dipole moment | 2.23 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 218.13 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -105.7 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -4267.9 kJ/mol |
| Hazards | |
| GHS labelling | GHS02, GHS05, GHS07 |
| Pictograms | GHS02,GHS05,GHS07 |
| Signal word | Warning |
| Hazard statements | H225, H302, H314, H411 |
| Precautionary statements | P210, P261, P264, P271, P280, P301+P312, P303+P361+P353, P304+P340, P305+P351+P338, P312, P330, P337+P313, P363, P370+P378, P405, P501 |
| NFPA 704 (fire diamond) | 3-3-2-ALPHA |
| Flash point | -12 °C |
| Autoignition temperature | 205 °C (401 °F; 478 K) |
| Explosive limits | 1.1–7.4% |
| Lethal dose or concentration | LD50 oral rat 290 mg/kg |
| LD50 (median dose) | LD50 (median dose): Oral rat LD50 = 235 mg/kg |
| NIOSH | UW2625000 |
| PEL (Permissible) | PEL: 5 ppm (parts per million) |
| REL (Recommended) | 5 ppm |
| IDLH (Immediate danger) | 250 ppm |
| Related compounds | |
| Related compounds |
Trimethylamine
Diethylmethylamine Ethylmethylpropylamine Dipropylamine Dimethylethylamine |
