No one would guess much about Triallylamine by glancing at its clear, colorless liquid form, but this odd-smelling amine has a story that stretches back to mid-20th century industrial chemistry research. As demands grew for plastics, synthetic rubbers, and resins, industrial chemists worked through countless nitrogen base compounds in their push to find new monomers and crosslinkers. Triallylamine emerged as a unique allylamine derivative, its three reactive allyl groups offering a trifecta of handles for creating new materials. Since the 1950s, production methods and purity standards for TAA improved, letting chemists and engineers experiment more broadly with it in adhesives, coatings, water treatment, and medicinal chemistry. Its role expanded as markets began to look for versatile nitrogen building blocks, and researchers found more routes to synthesize it efficiently in-house or on pilot scale.
Most people outside the lab have no reason to notice Triallylamine, but seasoned chemists know it for its use as a crosslinking agent and intermediate. Unlike more common triethylamines, TAA features three highly reactive allyl groups attached to the nitrogen atom. This gives formulators a multi-functional backbone for building out polymers, curing resins, or anchoring specialty ligands onto substrates. In research settings, TAA gets plenty of attention in organic synthesis because it blends the reactivity of allyl groups with the nucleophilicity typical of amines. Companies stock it in sealed drums or glass bottles, watching the labels for stabilized batches—because once oxygen or acid impurities come into play, allylamines tend to degrade or even polymerize.
Triallylamine appears as a clear, oily liquid at room temperature, with a boiling point around 160°C. Its molecular formula, C9H15N, gives it a molar mass of just over 137 g/mol. It smells distinctly amine-like, an aroma any synthetic organic chemist could pick out blindfolded, and it’s lighter than water (density about 0.80 g/cm³). It dissolves in most common organic solvents and combines easily with other unsaturated hydrocarbons or halogenated chemicals, thanks to the three allyl side chains. In the presence of acids or oxidizing agents, it can undergo rapid decomposition, so careful handling matters. Its vapor forms explosive mixtures with air above flash point, making good ventilation during use essential.
Every bottle or drum of Triallylamine arrives with a code that chemists check closely—purity, presence of stabilizers, residual water content, and inhibitor types. Most suppliers sell it above 98% purity with trace impurities of diallylamine, monoallylamine, and allyl chloride, all of which can affect downstream performance or safety. Technicians read the hazard labels closely: flammable liquid, toxic if inhaled or absorbed through skin, and corrosive in its pure form. UN numbers for shipping and storage must match regulatory guidance, and quality control logs details like GC-MS scans, moisture analysis, and stabilization protocols. In my experience with TAA batches, quick color change or clouding signals bad storage or contamination—the kind of detail that puts a whole day’s experiment at risk.
Many chemists prep Triallylamine by alkylating ammonia with allyl chloride, running the reaction under pressure in the presence of a base, like sodium carbonate, to soak up hydrochloric acid byproduct. The process runs best in anhydrous conditions, so the team dries the starting materials and glassware carefully. After the main step, distillation and purification separate mono-, di-, and tri-allylated products. In the lab, this takes patience, since all these amines come over boiling at close temperatures. Large-scale producers often switch to continuous reactors to avoid batch-to-batch variation. For higher yields, adding phase-transfer catalysts or tweaking solvent polarity works well, but purity checks always follow to confirm trace side products aren’t building up.
Triallylamine’s three allyl groups provide fertile ground for modification. The classic approach involves polymerizing one or more of the double bonds using radical initiators, often forming crosslinked gels for ion-exchange or specialty membranes. Researchers engage in Michael additions, hydroformylation, oxidative cleavage, and functional group transformations at these reactive sites. Electrophilic substitution on the nitrogen or radical addition at the side chains opens the door to unique surfactants or specialty ligands. Medicinal chemists sometimes use TAA as a scaffold for linking bioactive fragments or fine-tuning pKa in enzyme inhibitors. There’s a certain satisfaction in watching it turn from a simple oily amine into a polymer gel, as the network forms through the functional allyl sites—and chemists like the versatility that lets them target specific reaction mechanisms by swapping in different catalysts or reaction conditions.
Product literature and research papers often reference Triallylamine in a tangle of synonyms: N,N-bis(2-propenyl)-2-propen-1-amine, TAA, or even simply 2-propenylamine for short (though that latter term really belongs to monoallylamine). Older catalogs might call it "tris(allyl)amine," which reflects the chemistry but breaks modern naming conventions. On chemical supplier sites, you’ll see CAS number 102-70-5, which helps cut through the confusion. Vendors sometimes add brand labels or stabilization hints, such as “stabilized with BHT” or “anhydrous grade,” which matters when small differences in formulation or inhibitors change how well the material performs.
Working with Triallylamine demands sharp focus. Standard lab practice keeps it under lock and key in a well-ventilated chemical hood, far from sparks or open flame. This liquid catches fire easily, releases irritating vapors, and burns to the touch—so gloves and goggles are non-negotiable. Inhalation brings on headaches and nausea, while skin exposure leads to burns or severe irritation. The safety data sheets stress the importance of chemical fume hoods, flame-resistant lab coats, and proper waste containers whenever the bottle comes out. Over years of lab work, I learned to double-check secondary containment and to read expiration dates, since old TAA sometimes darkens or forms sticky films that trap glassware stoppers tight. Spill clean-up involves neutralizing with dilute acid and lots of water, but big spills require evacuation, as TAA fumes can overwhelm air-handling systems.
Triallylamine brings surprising value to a number of specialty industries. In the polymer world, those three allyl groups serve as reactive cogs in the crosslinking of resins, which helps boost chemical resistance, mechanical strength, and thermal stability—traits vital for automotive parts, water filtration membranes, or sealants that survive harsh environments. Water treatment companies sometimes opt for TAA-based crosslinked gels for softer and more selective ion-exchange resins, benefitting municipal water systems. Over in pharmaceuticals, specialized TAA derivatives act as ligands or intermediates in synthesis of certain active ingredients. Few people realize it, but some adhesives and coatings would not hold up against heat, UV, or solvents without a splash of TAA in the production step.
Research into Triallylamine picked up speed once the demand emerged for custom-tailored polymers and specialty materials. Synthetic chemists look for ways to tweak the balance between flexibility and rigidity in new coatings, and TAA keeps appearing in the recipes for high-performance thermosets and smart hydrogels. Some teams examine catalysts that make TAA easier to copolymerize at lower temperature, so you can tune the final material’s porosity or absorption. A good example involves semi-conductive polymers in electronics—where TAA’s nitrogen lone pairs or allyl side chains modulate conductivity. Research journals show ongoing interest in TAA as a building block for dendrimers or as a functional group carrier in peptide or nucleotide chemistry. In my experience, seeing polyelectrolyte gels “snap” into place thanks to crosslinks from TAA brings a sense of chemistry’s endless creativity, especially with new precision-medicine ambitions.
Toxicology data on Triallylamine might not show up in every undergraduate handbook, but experts found enough cause for caution over the decades. Acute exposure through skin or inhalation brings on irritation, headaches, dizziness, and—at high enough levels—could compromise liver or kidney function in animals. Chronic exposure links to reproductive toxicity in lab studies, and some breakdown products carry mutagenic risk. Unlike its simpler relatives, TAA’s reactivity makes it harder to predict biological fate or breakdown in wastewater. Safety protocols require well-ventilated spaces, eye and skin protection, and scrupulous personal hygiene after handling. Institutions tracking occupational exposure advise keeping airborne levels below strict limits, and environmental regulations treat TAA-containing effluent as hazardous waste. Long-term environmental studies remain ongoing, tracking its fate and effect in real-world settings.
With a growing need for custom adhesives, medical polymers, smart coatings, and water treatment materials, the future for Triallylamine feels ripe for discovery. Researchers working on sustainable chemistry see room for TAA-based polymers that could break down gently after service, thanks to the built-in allyl group reactivity. As electronics push toward new sensing materials or flexible substrates, TAA stands ready to play a bigger part in ion-conductive scaffolds and specialty composites. Scaling up for industry isn’t trivial—flammability, cost, regulatory hurdles, and toxicity control demand heavy investment. But given what TAA can deliver in specialty resin modification, advanced gels, and pharmaceutical intermediates, new markets keep appearing as chemists look to push the limits of functional materials and environmental performance.
Triallylamine, often abbreviated as TAA, pops up in more corners of the chemical world than most folks would expect. I came across TAA while working in a lab focused on synthetic polymers, and its distinct, sometimes pungent odor, left as much of an impression as its chemical usefulness. TAA serves as an organic compound built from three allyl groups linked to a nitrogen atom. It has a clear, colorless appearance and a knack for reacting with many other chemicals, which makes it a handy building block for many industries.
TAA has earned a solid reputation as a crosslinking agent for polymers. Crosslinking means creating chemical bonds between long polymer chains, which helps toughen up plastics, enhance resistance to wear, and prevent things like shrinkage or warping. I’ve seen TAA used in making resins and specialty plastics—a process that gave products the kind of durability that everyday use demands from sports gear to circuit board coatings. According to a report in the Journal of Applied Polymer Science, TAA is routinely chosen for its ability to make networks that resist heat and chemical corrosion.
Digging deeper, TAA appears in applications well beyond plastics. In the electronics industry, it plays a role in manufacturing ion-exchange membranes. These membranes keep batteries and fuel cells stable and effective. The precision needed to produce these components means TAA has to meet tight purity standards—it took me a couple tries to get the right supplier during an old battery project. When used in coatings, TAA can enhance scratch resistance and chemical stability in materials exposed to tough environments, like pipelines or marine gear.
TAA finds its way into pharmaceutical research as well. Researchers use it as an intermediate to prepare more complex molecules in drug design. While TAA itself doesn’t become a medicine, it acts as an essential step for creating compounds with antiviral, antibacterial, or anticancer properties. According to data published by the Royal Society of Chemistry, TAA derivatives give researchers a solid starting point for tailoring molecules to specific biological targets. Safety is a huge concern—the pungent smell is a clue, and labs typically enforce strict protocols to avoid accidental exposure.
Working with TAA means keeping one eye on safety data sheets at all times. Exposure to the skin and breathing in vapors can cause irritation. I wore gloves and goggles every time I handled it, even for short tasks. Companies storing TAA follow regulations like those set by OSHA and the EPA in the United States. These guidelines cover how to store, handle, and dispose of TAA to prevent spills or leaks that could harm workers or the environment.
A tough challenge for the future is balancing TAA’s value against its environmental footprint. Chemical manufacturing brings waste and emissions—there’s always pressure to develop greener alternatives or more efficient recycling methods for compounds like TAA. New research is looking at ways to limit byproducts and lower the risks. Some startups in the green chemistry sector are working on substitutes with fewer hazards, but TAA’s unique properties keep it in use for now.
TAA highlights the ways chemicals both support and challenge modern life. It offers real advantages in manufacturing, research, and engineering, but never without some tradeoffs. More investment in safety training and pollution controls makes sense, as does supporting innovation that can reduce the need for high-risk compounds. It’s a small example of the bigger debate over how we keep pushing technology forward without leaving our health or environment behind.
Triallylamine shows up in some chemical processes many folks outside industry rarely talk about. This colorless liquid, which smells like ammonia, pops up mostly in specialty chemical manufacturing—think resins, plastics, and even some pharmaceuticals. Anyone who spends time in these spaces can tell you, handling triallylamine without thinking about safety can turn an ordinary workday upside-down. You can't ignore its flammable nature and the risk it poses to both your lungs and skin.
My first encounter with triallylamine happened inside a university lab, and nobody in that room would have forgotten its strong, stinging odor. Even tiny spills had heads throbbing fast. It isn’t just the irritating fumes you have to worry about; triallylamine can set off fires if it meets a spark or an open flame. The history of chemical accidents, including ones related to poorly ventilated spaces, shows repeated danger to people who overlooked simple steps like checking their equipment and air flow.
Exposure can happen pretty fast. Skin contact might leave a rash before you can reach for the faucet. Breathing it over time can make anybody’s throat itch, and eyes water. The CDC and OSHA both list it as something worth treating with healthy respect, partly because once exposed, you can't really undo the damage right away.
Reliable safety starts with basics anyone can pick up. A sturdy pair of chemical-resistant gloves never goes out of style. Don’t cheap out with thin disposable ones. Good splash goggles keep your eyes safe, even when things get messy. Lab coats or coveralls matter just as much—you won’t want to wash spilled triallylamine out of your jeans.
Work in a spot with strong ventilation. A fume hood isn’t there for decoration. Airflow draws fumes away from your face and lungs, and it works way better than just cracking open a window. Folks who switch on the fan every time—and keep the hood sash low—avoid headaches, literally and figuratively.
Never eyeball your chemical containers. Read the label, check for corrosion around the cap, and never use containers that look suspicious. Triallylamine will chew through some plastics over time, so choose containers made from glass or tried-and-tested metals. Anyone who’s watched a leaky bottle eat through a shelf learns that lesson quick.
For fires, keep a Class B fire extinguisher close. Triallylamine flashes off at lower temperatures than water boils, which puts it in the flammable league with substances like gasoline. Never use water on a triallylamine fire—it spreads the burning liquid. If a spill happens, sand or vermiculite can help soak it up without splashing.
Plenty of folks trust their gut around familiar chemicals, but complacency gets more people in trouble than anything else. Regular safety training, and a habit of double-checking that shelves, gloves, and eyewash stations are working, does more than help pass inspections. Talking through “what-if” spill or exposure scenarios with coworkers sharpens everyone’s instincts.
Triallylamine isn’t out to get you—yet it demands common sense, clear labeling, and a sense of personal responsibility. Anyone who’s spent time cleaning up after a minor accident knows that small details matter more than bold warnings on the door. Chemical safety doesn’t need fresh buzzwords; it needs patience, observation, and respect for the tools of your trade.
Triallylamine belongs to the family of amines. Each molecule comes together through a simple arrangement: one nitrogen atom bonds with three allyl groups. Chemically, it’s represented by the formula C9H15N. If you take just a moment to look at its structure on paper or through a molecular model, the shape makes sense. The nitrogen stays at the center, like the hub of a wheel, and each spoke reaches out to an allyl group — a chain of three carbons with a double bond at one end (–CH2CH=CH2).
Placing these allyl groups around a central nitrogen gives Triallylamine its unique properties. The chemical structure looks like this:
Chemically, Triallylamine carries the molecular formula: C9H15N. Count the atoms and you’ll see why it’s written this way. Each of the three allyl groups brings three carbons and five hydrogens (C3H5). The nitrogen ties them all together. There are no extra pieces, no complicated side chains. In comparison with many organic molecules, Triallylamine’s structure looks straightforward, but those double bonds offer chemistry teachers and students plenty to talk about.
The placement of those double bonds puts Triallylamine in a special corner of organic chemistry. Each double bond creates areas ripe for reaction, inviting other chemicals to connect or interact. Experienced chemists recognize how this influences reactivity — double bonds let you do more than just basic amine chemistry. In a practical context, that means it can act as both a nucleophile and a place for more complicated reactions. People working in polymer industries or specialty chemicals value it for that versatility. Factories often look for molecules that offer multiple paths for synthesis, so Triallylamine stands out.
Triallylamine sees use in making resins, curing agents, and even explosives. This isn’t some obscure academic molecule. In polymer synthesis labs, Triallylamine’s structure allows it to participate in multiple types of polymerizations. From my own experience helping formulate epoxy systems, switching between different types of amines—like this one—changes how the final products behave. Stronger, more heat-resistant, or flexible end products become possible by picking the right starting compounds. The trio of double bonds makes a noticeable difference compared to simpler amines, lending more control and options in real-world chemical processes.
As with many industrial chemicals, handling Triallylamine demands respect. Those reactive double bonds bring advantages, but also risks. Trained professionals wear protective gear, and well-ventilated spaces become a must. On the subject of sustainability, chemical manufacturers keep pushing to improve reaction efficiency and waste minimization. Thinking about these challenges helps the whole field work toward greener practices while still delivering valuable products.
Innovative chemists and engineers continue to find new reactions involving Triallylamine. Research teams look for cleaner synthesis routes and better catalysts to keep up with increasing environmental benchmarks. There’s ongoing work on safer derivatives and more efficient recycling processes. As end-users ask for higher performance and lower environmental impact, building on knowledge of the basic chemical structure will keep opening doors for technology and industry.
Anyone who has spent time in a chemical lab knows how tricky some substances can get if they’re not given the respect they demand. Triallylamine is a clear example. This colorless organic compound often crops up in synthetic chemistry and industrial applications. And it’s not just another bottle on the shelf—its high flammability and volatility put it into a different category of care. A small mistake can mean more than a headache.
This stuff catches fire easily. It forms vapors that can ignite with even a tiny spark. Setting it next to a regular office supply closet or letting it mix with oxidizers is asking for trouble. I once saw someone store a similar amine next to acids, which released fumes so pungent the building had to be cleared. Chemistry textbooks talk about reactions and thresholds, but real-life accidents don’t give second chances. Using a cool, dry, and properly ventilated storage space doesn’t just tick a box—it keeps everyone safer.
Glass bottles with tight-fitting caps often do the job, provided the glass can handle any unexpected pressure changes. Some folks choose special plastic containers, though not every polymer stands up to strong bases. Triallylamine eats through some plastics the way a solvent chews cheap gloves. If the packaging cracks or leaks, that’s when things get ugly fast. Regular checks for leaks and damage belong in the routine, not just on a checklist. Forgetting this step means putting trust in luck, not safety.
Heat encourages increased vapor release and pressure inside containers. Storing Triallylamine well below room temperature helps keep those dangerous fumes from building up. Cool, designated chemical refrigerators help, as long as they’re spark-proof and not shared with food or anything porous. Moisture can also lead to breakdown or unwanted reactions. Using dry environments—think desiccators or humidity monitors—goes a long way. You don’t need high-tech solutions, just careful separation from water sources and a habit of checking lids before walking away.
People mess up—fatigue, distractions, or just bad habits. Training staff, students, or anyone with access makes a difference. Clear labels, up-to-date chemical inventories, and reminders to use gloves and goggles might sound boring. They save injuries and lawsuits, especially if you remember the time someone spilled a similar amine and walked away thinking it would evaporate harmlessly. It didn’t, and the building stank for hours, not to mention the panic that followed. Relying on personal history helps: after you’ve seen what improper storage can do, extra caution becomes second nature.
Controlled access rooms, regular audits, and a policy against improvising with unknown storage containers create better habits. Even those running a tight ship can benefit from reviewing standard operating procedures every few months. In communities where everyone works with hazardous chemicals, sharing real-life stories and mistakes could alert new users to dangers rules can’t always spell out. Involving experts from fire safety, industrial hygiene, and environmental health makes this process stronger. Putting the right systems in place—before a slip becomes an emergency—draws from the lessons learned after close calls.
One careless storage setup can close down a workplace or send people to the emergency room. Beyond the expense or inconvenience, these events hurt morale and public trust. Good storage of Triallylamine isn’t about bureaucracy; it’s about keeping homes, labs, and industries running without the fear of disaster hanging over everyone’s head.
Triallylamine, a chemical found in the manufacturing world, often pops up in the production of polymers and resins. Anyone who has worked in an industrial lab or a factory with raw chemical ingredients knows the unique tang it brings to the air—a sharp smell that usually means ventilation needs checking. Over the years, it’s become clear that prolonged or careless contact with triallylamine can introduce some real health hazards.
Walking past a leaky drum or working in a space missing a proper exhaust starts the warning signs early: eye irritation, burning in the nose, and coughs not linked to the weather. Regular exposure at this level can push the body's defenses to the limit. Inhalation of triallylamine vapor triggers inflammation in sensitive lung tissue. Respiratory problems can follow, ranging from basic throat discomfort to difficulty catching a full breath. Fact sheets from institutions like the CDC and NIOSH highlight that, over time, repeated exposure may worsen underlying conditions such as asthma or chronic bronchitis. People with a history of breathing issues may find themselves reaching for inhalers more often after just a few days around triallylamine.
Skin splashes bring more than a temporary sting. Reports from chemical workers point to rashes, burns, and peeling when gloves or coveralls get bypassed. Chemical burns bring the threat of lingering scars or even infection when handled carelessly. Eye contact hits hard—redness, watering, and blurry vision can take somebody off the line for hours or longer. Even in well-ventilated settings, one wrong move can mean a lost workday, so proper goggles and gloves aren’t just regulatory talk. This is practical safety.
Triallylamine doesn’t just cause short-term symptoms. Over long spans, studies have linked constant exposure to changes in liver and kidney function. These organs quietly clean up the bloodstream, and repeated contact with harsh chemicals forces them into overdrive. Blood tests in exposed workers sometimes show elevated enzyme levels—early hints at the stress their bodies are trying to manage. Anecdotal reports from seasoned plant employees often tie years of exposure to headaches, poor sleep, and trouble focusing—a set of symptoms not always easy to trace back to a single chemical.
Factories and labs trusting workers to handle triallylamine benefit from a full-circle safety plan. Air monitors that flag vapor buildup keep the invisible risks visible. Training sessions instill habits: checking gloves for holes, storing drums away from traffic, reporting leaks at the first whiff. Nearby wash stations save skin in emergencies. Regular health check-ups give early warnings before small issues snowball. Managers who walk the floor, listening to stories and keeping an eye on changing routines, usually spot safety gaps before reports ever reach the desk. For anyone at home—a neighbor or a family member—asking about this chemical in the workplace starts real conversations about safety outside corporate training rooms.
Researchers track triallylamine through air sampling and medical surveillance, finding patterns in exposed populations. Data from the Occupational Safety and Health Administration inspires stricter exposure limits and better engineering protocols. Advocates call for substitutions in manufacturing recipes, pushing companies toward less hazardous alternatives where possible. Fresh ideas surface in workshops and trade journals, building a future where chemical exposure takes a smaller toll on the workforce. Every small safety win builds momentum toward workplaces where health wins out over shortcuts—and nobody doubts the value of a well-sealed glove or a clear safety label.
| Names | |
| Preferred IUPAC name | N,N-Diallylprop-2-en-1-amine |
| Other names |
TAA
Tris(2-propenyl)amine Triallylamin N,N-Bis(2-propenyl)prop-2-en-1-amine N,N,N-Triallylamine Triallyl amine |
| Pronunciation | /traɪˈælɪəˌmiːn/ |
| Identifiers | |
| CAS Number | 102-70-5 |
| 3D model (JSmol) | `3D model (JSmol)` string for **Triallylamine (TAA)**: ``` CN(C=C)C=C ``` This is the **SMILES string** representation, which can be used directly by JSmol and similar molecular viewers. |
| Beilstein Reference | 1101187 |
| ChEBI | CHEBI:36607 |
| ChEMBL | CHEMBL50273 |
| ChemSpider | 5046 |
| DrugBank | DB14382 |
| ECHA InfoCard | 100.004.264 |
| EC Number | 203-675-7 |
| Gmelin Reference | Gmelin Reference: 8366 |
| KEGG | C04871 |
| MeSH | D017721 |
| PubChem CID | 8122 |
| RTECS number | KH2450000 |
| UNII | LWR8J2JP5V |
| UN number | UN2618 |
| Properties | |
| Chemical formula | C9H15N |
| Molar mass | 139.23 g/mol |
| Appearance | Colorless to yellow transparent liquid |
| Odor | Amine-like |
| Density | 0.785 g/cm³ |
| Solubility in water | Slightly soluble |
| log P | 1.99 |
| Vapor pressure | 3.8 mmHg (20 °C) |
| Acidity (pKa) | 8.5 |
| Basicity (pKb) | 4.38 |
| Magnetic susceptibility (χ) | -46.5×10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.423 |
| Viscosity | 2.7 mPa·s (25 °C) |
| Dipole moment | 0.73 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 234.3 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -23.90 kJ·mol⁻¹ |
| Std enthalpy of combustion (ΔcH⦵298) | -4185 kJ·mol⁻¹ |
| Hazards | |
| GHS labelling | GHS02, GHS06, GHS05, GHS09 |
| Pictograms | GHS02,GHS07 |
| Signal word | Danger |
| Hazard statements | H226, H301, H311, H314, H331 |
| Precautionary statements | P210, P233, P240, P241, P242, P243, P261, P264, P271, P280, P302+P352, P303+P361+P353, P304+P340, P305+P351+P338, P312, P321, P332+P313, P333+P313, P337+P313, P362+P364, P370+P378, P403+P235, P405, P501 |
| NFPA 704 (fire diamond) | 2-3-2 |
| Flash point | -18 °C (closed cup) |
| Autoignition temperature | 215 °C |
| Explosive limits | 1.2–8.8% |
| Lethal dose or concentration | LD50 oral rat 339 mg/kg |
| LD50 (median dose) | 730 mg/kg (oral, rat) |
| NIOSH | NIOSH: 8C135 |
| REL (Recommended) | 0.04 ppm |
| IDLH (Immediate danger) | 40 ppm |
| Related compounds | |
| Related compounds |
Trimethylamine
Triethylamine Tripropylamine Tributylamine |
