DMAA popped up on the chemistry scene as the acrylic industry grew legs in the middle of the last century. As research labs looked for ways to improve polymers and hydrogels, DMAA started lifting its weight. Its journey owes a lot to demand for materials that absorb water without falling apart and for modifiers that play nice with water and oil. Acrylic polymers weren’t always the best at flexing with environmental needs. DMAA’s chemical quirks helped engineers and scientists shuffle properties like flexibility and water absorption without heavy trade-offs. Over time, it went from lab curiosity to a staple ingredient in manufacturing that expects more from its plastics, coatings, and gels.
DMAA is widely sold as a colorless, clear liquid. Its job often involves copolymerization, where it links up with other monomers to form polymers that bring something extra to the table—like increased softness or water-compatibility in finished products. Labs, plant managers, and formulators pay close attention to its purity, since trace water or residual stabilizers can mess with how it performs. It can show up in drums or totes, but always needs airtight seals, since moisture causes headaches by starting unwanted reactions or polymerization right in the barrel.
This compound brings a molecular weight of about 99.13 g/mol and has a boiling point in the neighborhood of 214°C. It pours out with a density close to 0.96 g/cm³ at room temperature. Chemists like how easily it dissolves in water, methanol, and other polar solvents, which opens doors for formulating gels, medical coatings, and adhesives. DMAA comes with a faint, fishy smell—hard to miss if you work in a lab long enough. Left uncovered, it doesn't quickly evaporate thanks to its low vapor pressure, but its double bond makes it sensitive to light and air, so storage in dark, cool places isn’t just a suggestion.
Industry standards ask for purity above 99% for most technical and research work. Any supplier worth their salt labels their DMAA to spell out water content, acid numbers, stabilizer type, and potential inhibitor concentrations. Labeled details track lot numbers for traceability, with UN numbers attached to legal shipping—DMAA typically travels under UN 2056, not flirting with dangerous goods categories unless its volume spikes. Technical data sheets will go deeper, noting viscosity, refractive index, and stabilizer profiles, along with safe temperature and light exposure limits during storage.
DMAA often gets synthesized through the reaction of acryloyl chloride with dimethylamine, yielding the amide group that defines its structure. This approach calls for good ventilation and skilled hands, since starting materials aren’t friendly to skin or lungs. Labs doing this on a large scale employ closed reactors, chilling systems, and scrubbers for off-gassing hydrochloric acid. After synthesis, distillation helps remove unreacted precursors. If you ever step into a plant while DMAA is distilling, the focus on temperature control and contamination avoidance speaks volumes about priorities in chemical manufacture.
DMAA stands out in copolymerization. It partners with acrylamide, acrylic acid, or other methacrylic monomers to build polymers that target specific uses, like water-absorbent hydrogels or flexible coatings. Its dimethyl groups boost hydrophilicity and keep finished products from drying out or cracking. DMAA’s reactive vinyl group opens the door for further functionalization—adding quaternary ammonium groups, for instance, enhances antimicrobial properties or boosts ion-exchange capabilities. Labs exploring crosslinked networks often use DMAA to fine-tune the balance between stretchiness and absorbency in their gels.
You’ll find DMAA labeled as N,N-dimethyl-2-propenamide, 2-propenamide, and dimethylacrylamide in technical catalogs. Some supply chains abbreviate it as DMAA, while others rely on brand names with series numbers tied to specific polymer types. Keeping track of synonyms prevents confusion during inventory and purchasing, since similar-sounding compounds can lead to expensive mistakes in production batches.
Working with DMAA means gloves, goggles, and lab coats as baseline protection. Its liquid can irritate eyes, skin, and upper respiratory tract on contact. Health and safety teams usually keep chemical fume hoods humming to keep exposure under control. DMAA in storage requires sealed containers and a dry, well-ventilated area with clear “flammable” labels. Spill response has strict protocols: absorbents and double-bagged waste, all while avoiding discharge into drains. SOPs stress the importance of training on first aid and spill containment, especially for new staff or students.
DMAA holds its ground in industries where polymers need to balance strength and water response. One of its earliest and most successful uses involves hydrogels for soft contact lenses. The comfort factor here links straight back to the way DMAA copolymers hold onto water while staying tough under wear and tear. Medical fields use DMAA-derived gels in wound dressings, where they protect and promote healing by managing moisture. In papermaking, DMAA-modified resins fine-tune paper texture and help control ink absorption. You’ll also see DMAA pop up in adhesives, printing plates, and even hair care products where it helps build body and manage static through better polymer-film formation.
Research labs track DMAA closely as they hunt new materials for biomedicine and electronics. Scientists experiment with new crosslinkers and chain extenders to create hydrogels that swell with more control or show targeted drug release profiles. Others take DMAA into nano-scale projects, embedding drugs or catalysts inside crosslinked matrices for more precise delivery or detection. These R&D efforts lean on DMAA’s established track record in biocompatibility and manageable toxicity, which helps clear regulatory hurdles faster.
Toxicologists have spent years tracking DMAA’s effects. Acute exposure to the neat liquid causes irritation and sometimes sensitization in skin and eyes. Longer term, the risk profile improves—DMAA isn’t mutagenic under most laboratory conditions, and animal studies point to a reasonably safe handling bracket when exposures are kept low. The risk spikes with heated vapors or large spills, which reinforces the need for engineering controls in plants and proper ventilation in labs. Waste handling stresses containment and careful incineration to block environmental release.
DMAA keeps proving itself as demand grows for smarter polymers. In healthcare, it’s paving paths in drug delivery and tissue scaffolding, thanks to its biocompatibility and adaptable network structures. Plant-based and renewable chemistry are making inroads, too, with DMAA building bridges between green monomers and flexible, high-performance materials. Electronics and soft robotics need polymers that flex and bend without breaking—a space where DMAA copolymers already make an impact. Looking ahead, advances in sustainable synthesis and tailored crosslinking could keep DMAA relevant as industries chase better, safer, and greener plastics.
N,N-Dimethylacrylamide, typically abbreviated as DMAA, has been showing up in places people rarely talk about, yet it keeps many modern products working as they should. This chemical holds a strong reputation in the plastics and polymer industries. DMAA brings flexibility and water compatibility to resins that manufacturers shape into films, coatings, and adhesives.
Products made with DMAA tend to stay clear and tough, resisting the yellowing and harsh wear you might see in cheaper plastics. Paints that cling well to a surface and textile finishes that stretch but don’t lose shape often contain a bit of this chemical magic. These features matter when I look around at things built to last longer and keep up with daily use.
A place where DMAA really makes a noticeable difference is water treatment. Water companies want polymers that soak up dirt and particles without gumming up the process. DMAA-based polymers attract water, so filters using them capture tiny bits that slip past other materials. The impact here ripples into homes—drinking water arrives clearer, and fewer chemicals land in our bodies. That’s something I personally value every time I make coffee or run a bath.
In the personal care industry, DMAA stands quietly behind many gels, lotions, and even contact lens solutions. It keeps products smooth and less sticky. That might sound trivial, but anyone who deals with stained shirts from greasy creams or blurry lenses will appreciate how small chemical tweaks can mean big comfort.
DMAA-enhanced polymers improve toner adhesion in printers and help form glossy, strong finishes on magazines and labels. Those vibrant labels that survive a week in the fridge owe a nod to the ingredient list on the back—and, buried among them, to DMAA. In electronics, flexibility is everything. Polymers using DMAA let circuit boards bend instead of break. As demand grows for wearable gadgets and foldable phones, reliable chemicals like DMAA let engineers keep pushing the limits.
Transparency matters whenever chemicals touch so many corners of life. Studies suggest DMAA doesn’t build up in the body, and plant workers follow safety rules set by agencies like OSHA and the EPA. Big accidents stay rare, but spills can happen. At work, anyone handling DMAA uses gloves, goggles, and good ventilation. Those steps come from lessons learned in the past—safety roots itself in experience, not just labels and manuals. I remember a colleague who once brushed off goggle rules and paid with days of eye trouble. Approaching any chemical with care isn't just formality—mistakes hurt real people.
No single ingredient stands alone without questions about the future. DMAA delivers clear benefits, but the urge to cut petroleum-based chemicals grows. Some labs now explore bio-sourced monomers. Regulatory focus pushes for less waste and greener disposal methods. I’ve seen industry events where leaders talk up newer, safer formulas—trials that replace parts of the molecule with plant materials or look for better breakdown in the environment. It’s not easy, but pressure to shape a safer world keeps teams innovating.
DMAA may stay in the background of daily life, but understanding its role reminds us that smart choices in chemistry ripple out. Each new improvement draws from the lessons—and the responsibility—shared by everyone who uses, studies, or lives alongside these modern materials.
N,N-Dimethylacrylamide, often called DMAA, gets a lot of attention in labs that use specialty polymers or want certain physical properties in their gels. Anyone who has handled this chemical knows it doesn't behave like table salt or the average lab solvent. The Material Safety Data Sheet gives a snapshot, but day-to-day experience says even a small bit of sloppiness can cause problems you don’t want in your workroom.
DMAA isn’t water, and it certainly isn’t something you want splashing on your skin. A bit of it on your hands feels sticky, and the smell from even small spills grabs your attention. Its vapor isn’t pleasant, and I’ve seen new lab workers learn the hard way not to leave containers uncapped. Over time, DMAA can react with oxygen or acids and form compounds that increase the chance of it doing unwanted things—polymerizing in the bottle or releasing vapors you would rather not breathe.
Keep DMAA tightly closed in a spot that stays cool and dry. Temperatures between 2 and 8°C do the trick, which means most labs put it in a refrigerator reserved for chemicals—never in the same fridge as your lunch. Leaving DMAA on a sunny bench or a shelf near radiators makes it spoil faster or even triggers reactions you don’t want. Polymers can start forming inside the bottle, which ruins your supply and puts you at risk for a pressure buildup.
Containers matter, too. Glass or HDPE bottles with solid, chemical-resistant caps keep this chemical from getting out—no aluminum foil or makeshift stoppers. I’ve seen folks decant into smaller bottles, labeling each with the name and the date of transfer. It sounds basic, but that step saves more headaches than you might expect, especially in busy labs with lots of hands in and out of storage.
Humidity is a sneaky enemy. DMAA absorbs water out of the air, and each day it sits open to the room, the more water you end up with in your supply. This isn’t just a purity issue—it messes with your reactions and changes the way your product comes out. Keeping the bottles tightly closed and away from damp spots—in other words, steer clear of fume hoods where condensation forms or sinks where water splashes—is a habit worth building.
Direct sunlight also speeds up breakdown. Any bench space with glass windows nearby turns into a tiny oven and chemical reactor. So, store DMAA in an opaque cabinet or a chemical fridge, with a log showing who takes what and when. That usually helps spot problems before a bad batch ends up in your experiment.
DMAA has a flash point around 95°C, so it’s not harmless. Spills near electrical gear or flame sources spell trouble. Keeping a chemical-resistant spill kit nearby isn’t just overkill—it’s preparedness. In practice, folks use gloves and safety glasses every time, and chemical waste goes straight into the right bin, not down the sink. Even a rinse with DMAA on it finds its way into hazardous waste containers.
In my experience, the surest way to safe storage comes down to training, regular label checks, and a hard rule against quick-fix solutions in the lab. That keeps DMAA—and everyone working with it—safe from the kinds of mistakes that turn a regular workday into an emergency.
Anyone working with N,N-Dimethylacrylamide (DMAA) learns pretty quickly that purity is the line between disaster and reliability. Traces of sodium or volatile organics don’t just ruin results, they can destroy apparatus or build up regulatory troubles nobody wants to face. DMAA serves as a core monomer in water-soluble polymers, hydrogels, and medical materials, and purity can turn safe compounds into real headaches or, worse, stop a project from ever reaching scale-up.
Unlike buzzwords tossed around in marketing, purity specification isn’t just a badge manufacturers stick on bottles. Most DMAA products land at 99% pure or higher. That’s not a coincidence. The difference between 95% and 99.5% doesn’t look big on paper until a trace contaminant tweaks your polymer structure or grabs a regulator’s attention. I’ve seen research groups lose six months and thousands in funding after ignoring “insignificant impurities” lurking in monomer stocks.
For DMAA, users and regulators check for methylacrylic acid, dimethylaniline, aldehydes, and water content. Numbers carry weight: water should stay under 0.1%, and heavy metals need to sit below the part-per-million range. Neglect here means compromised finished products, whether in medical devices or specialty coatings.
Stories from the polymer industry keep leaking out. Poorly purified DMAA can cause stubborn gels or unpredictable viscosity. For medical applications, impurities endanger biocompatibility, ruin consistency, and push FDA approval much farther down the road. Chemists in advanced labs talk about failed batch records caused by bad DMAA. The need for consistency carries through supply chains, driving buyers to grill suppliers about their purification techniques—not just the number stamped on a cert.
Avoiding headaches starts in production. Reputable vendors rely on vacuum distillation and column purification to kick out trace monomers and metal ions. Chromatography confirms what distillation doesn’t catch. Some companies will run DMAA through a polymerization-depolymerization process just to drag out stubborn organics. Nobody likes the cost, but cutting corners bites you with recalls and regulatory delays later on.
Testing for DMAA purity gets heavy. Buyers demand gas chromatography-mass spectrometry (GC-MS) or high-performance liquid chromatography (HPLC) data for every batch. Certificates should spell out percentages for DMAA itself along with limits on water, sodium, heavy metals, and individual impurities. Labs often run in-house checks before signing off, since public data only goes so far.
Global regulations don’t offer shortcuts. The European Union’s REACH standards and the US FDA sit ready with their own checklists. A certificate of analysis without supporting chromatograms or method details usually gets pushed aside.
One way forward puts more control in the hands of researchers and buyers. Testing incoming DMAA lots avoids finger-pointing when experiments go sideways. Open communication between suppliers, chemists, and quality control departments lowers the risk of bad batches trickling downstream. Spot checks keep everyone honest, and regular audits encourage best practices.
I side with groups that demand regular documentation of procedures, chromatography results, water content, and heavy metal checks from vendors. A close relationship with a supplier, regular feedback, and not shying away from returning materials when purity slips draw better results in the long run. The bottom line: DMAA purity may look like a detail, but it shapes the safety, cost, and pace of every project it touches.
N,N-Dimethylacrylamide has found a place in many industrial and research settings. Its use in polymer development shows up in things ranging from coatings to water treatment formulations. People handling DMAA often wear goggles and gloves, respecting the warnings stamped on packaging, but concerns about its health and environmental impact warrant a closer look.
The data on DMAA draws from toxicology studies and regulatory agencies. DMAA can irritate the skin, eyes, and respiratory tract. Direct contact commonly brings out redness or itchiness, especially after spills or splashes. Inhalation presents more of a concern in industrial environments where vapor or mist lingers. Some people experience headaches or nausea in unventilated rooms.
The real trouble unfolds at chronic exposure or with poor handling. Animal testing shows DMAA has a low order of acute toxicity—meaning outright poisonings are unlikely in standard job uses—but that doesn't clear it from all safety concerns. The chemical can still trigger allergic reactions, and signs point to organ effects if inhaled or absorbed over weeks or months, especially at high concentrations. For years, German and Dutch chemical safety authorities have called DMAA a substance 'under suspicion' for long-term health issues.
DMAA's role doesn't stop at human contact, as accidental releases into local waterways or soil carry downsides. It moves easily in water, doesn't break down fast, and can reach sensitive ecosystems. Aquatic life absorbs chemicals fast, and studies show small creatures—like daphnia or fish eggs—show signs of stress or stunted growth after exposure. While DMAA doesn't rank near the most hazardous compounds released by industry, its persistence means mistakes stick around, especially near chemical manufacturing hubs.
Based on work in university labs and plant settings, practical safety steps matter more than ever. Well-maintained ventilation pulls vapors away before they can drift toward people. Chemical splash goggles and gloves, not just any old gloves but ones rated for acrylamide exposure, keep hands protected. Clean-up kits should be quick to reach, and spill response training keeps incidents from becoming nightmares. Employers can invest in regular air monitoring to spot problems before symptoms show up in staff.
Waste handling needs a careful approach. DMAA runoff never belongs in public drains. Specialized waste collection prevents routine disposal mistakes. Public agencies could support routine inspection and transparent reporting so everyone can track DMAA risks in their community and workplace.
Public health and chemical safety evolve when voices from the floor—researchers, workers, and neighbors—flag concerns early. Nobody expects zero risk from chemicals with active industrial use, but transparency and consistent safety steps help keep risks in check. DMAA deserves the respect shown to many hazardous industrial materials: handle it with awareness, not fear or neglect, and build knowledge out in the open. Regular updates to workplace guidelines, real-time reporting of any medical symptoms linked to exposure, and open datasets on environmental releases grow understanding over time.
In the real world of chemistry workshops and labs, no one chases after a monomer without a good reason. N,N-Dimethylacrylamide, often called DMAA by those who spend enough time around fume hoods, has a structure that lets it play some unique roles in polymer science. Sitting in a graduate research lab myself, I saw DMAA’s characteristics win over researchers: it dissolves in water and mixes with a broad range of other monomers, giving scientists room to experiment.
The big draw with DMAA centers on its ability to influence solubility and flexibility in finished polymers. Compared to acrylamide, DMAA resists hydrolysis and brings less charge to the party. That might sound technical, but it means products using DMAA become more stable and tolerate tougher conditions—think water treatment flocculants that need to handle shifting pH or medical hydrogels that can’t fall apart on contact with bodily fluids. Real-life trials show the copolymers stay clear, hold up under stress, and keep consistency longer than those built from less robust building blocks.
Lab-scale reactions prove straightforward. DMAA polymerizes easily with the same initiators used for classic acrylic monomers. Scaling up to industrial processes doesn’t call for specialized gear, and production keeps within the usual boundaries for energy use or equipment. That’s important: nobody wants a promising material you need to treat like a bomb just to manufacture it.
One sticking point comes from handling acrylamides in general—concerns over toxicity get tossed around. With DMAA, studies back up its lower toxicity compared to classic acrylamide. That said, safe handling procedures are drilled into anyone working with monomers, and the industry keeps one eye on regulator guidance, covering both worker safety and final product residues.
DMAA shines brightest where control over polymer traits means real commercial impact. Water treatment businesses look for ways to fine-tune flocculants for different climates and effluent profiles. DMAA delivers responsive, adaptable solutions. Medical device specialists turn to DMAA-based hydrogels to design wound dressings, contact lenses, or scaffolds for tissue engineering. One of my lab partners once produced hydrogels with DMAA that held more liquid under pressure, which makes a big difference for eye-care products needing extra comfort and sterility.
Synthetic chemistry rarely sits still. DMAA’s track record shows chemists want materials that can handle real-world problems, not just check off boxes in a spec sheet. In water treatment, DMAA lets engineers reach higher performance without blowing up costs or endangering workers. For biomedical specialists, its properties make it possible to deliver safer, more versatile devices.
Looking down the road, the push for greener, safer materials stands out as the next challenge. Researchers could find inspiration in DMAA’s low toxicity and tailor copolymer structures for recyclability or biodegradability. A future where polymers work harder and pollute less starts with choices like DMAA—monomers that get the job done safely and effectively, without locking us into yesterday’s solutions.
| Names | |
| Preferred IUPAC name | N,N-dimethylprop-2-enamide |
| Other names |
N,N-Dimethyl-2-propenamide N,N-Dimethylacrylamide DMAA Dimethylacrylamide Acrylic acid dimethylamide N,N-Dimethylethyleneamide |
| Pronunciation | /ˌdiːˌɛmˈeɪˌeɪ/ |
| Preferred IUPAC name | N,N-dimethylprop-2-enamide |
| Other names |
N,N-Dimethyl-2-propenamide DMAA N,N-Dimethylacrylamide N,N-Dimethylprop-2-enamide |
| Pronunciation | /ˌdiːˈem.eɪˌdiːˈmɛθ.əl.əˈkrɪl.ə.maɪd/ |
| Identifiers | |
| CAS Number | 2680-03-7 |
| Beilstein Reference | 1209280 |
| ChEBI | CHEBI:34968 |
| ChEMBL | CHEMBL1697837 |
| ChemSpider | 86573 |
| DrugBank | DB14035 |
| ECHA InfoCard | 03a3c4ed-c632-44b8-828c-bd20c9e8255a |
| EC Number | 203-652-6 |
| Gmelin Reference | 83048 |
| KEGG | C06510 |
| MeSH | D003587 |
| PubChem CID | 7488 |
| RTECS number | RR0350000 |
| UNII | XU6248F56T |
| UN number | UN2264 |
| CompTox Dashboard (EPA) | DTXSID2046934 |
| CAS Number | 2680-03-7 |
| Beilstein Reference | 635871 |
| ChEBI | CHEBI:78205 |
| ChEMBL | CHEMBL15706 |
| ChemSpider | 11089 |
| DrugBank | DB03768 |
| ECHA InfoCard | 03b57e4f-7acf-44e6-bc8c-98a755fe0396 |
| EC Number | 204-826-4 |
| Gmelin Reference | 61655 |
| KEGG | C19197 |
| MeSH | D003585 |
| PubChem CID | 7907 |
| RTECS number | AS3325000 |
| UNII | G9H36886QK |
| UN number | UN2264 |
| CompTox Dashboard (EPA) | DTXSID1022911 |
| Properties | |
| Chemical formula | C5H9NO |
| Molar mass | 99.13 g/mol |
| Appearance | Colorless transparent liquid |
| Odor | Amine-like |
| Density | 0.956 g/cm³ |
| Solubility in water | Miscible |
| log P | -0.77 |
| Vapor pressure | 0.56 mmHg (25°C) |
| Acidity (pKa) | 12.5 |
| Basicity (pKb) | pKb: 3.29 |
| Magnetic susceptibility (χ) | -7.34×10⁻⁶ cm³/mol |
| Refractive index (nD) | 1.4500 |
| Viscosity | 1.439 mPa·s (20℃) |
| Dipole moment | 3.35 D |
| Chemical formula | C5H9NO |
| Molar mass | 99.13 g/mol |
| Appearance | Colorless transparent liquid |
| Odor | Amine-like odor |
| Density | 0.956 g/cm³ |
| Solubility in water | Miscible |
| log P | -0.775 |
| Vapor pressure | 0.43 mmHg (20 °C) |
| Acidity (pKa) | 12.3 |
| Basicity (pKb) | pKb = 8.38 |
| Magnetic susceptibility (χ) | -7.73×10⁻⁷ cm³/mol |
| Refractive index (nD) | 1.450 |
| Viscosity | 1.32 mPa·s (20°C) |
| Dipole moment | 4.37 D |
| Thermochemistry | |
| Std molar entropy (S⦵298) | 225.6 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -161.5 kJ/mol |
| Std enthalpy of combustion (ΔcH⦵298) | -1956 kJ/mol |
| Std molar entropy (S⦵298) | 203.2 J·mol⁻¹·K⁻¹ |
| Std enthalpy of formation (ΔfH⦵298) | -161 kJ·mol⁻¹ |
| Std enthalpy of combustion (ΔcH⦵298) | -1831 kJ·mol⁻¹ |
| Hazards | |
| GHS labelling | GHS02, GHS07 |
| Pictograms | GHS07,GHS05 |
| Signal word | Warning |
| Hazard statements | H319: Causes serious eye irritation. |
| Precautionary statements | P280, P261, P264, P271, P304+P340, P312, P305+P351+P338, P337+P313, P501 |
| Flash point | 78°C |
| Autoignition temperature | 340°C |
| Explosive limits | 2.0%~11.0% |
| Lethal dose or concentration | Rat oral LD50: 2500 mg/kg |
| LD50 (median dose) | LD50 (median dose) of N,N-Dimethylacrylamide (DMAA): "3,200 mg/kg (rat, oral) |
| NIOSH | NIOSH: Not Listed |
| PEL (Permissible) | PEL (Permissible Exposure Limit) for N,N-Dimethylacrylamide (DMAA): Not established |
| REL (Recommended) | 10 ppm |
| IDLH (Immediate danger) | Not established |
| GHS labelling | GHS02, GHS07 |
| Pictograms | GHS07,GHS05 |
| Signal word | Warning |
| Hazard statements | H302, H319, H332 |
| Precautionary statements | P280, P261, P305+P351+P338, P304+P340, P337+P313 |
| NFPA 704 (fire diamond) | 2-2-2-W |
| Flash point | 82°C |
| Autoignition temperature | 340°C |
| Explosive limits | 5.2–14.2% |
| Lethal dose or concentration | LD50 (oral, rat): 2500 mg/kg |
| LD50 (median dose) | LD50 (median dose) of N,N-Dimethylacrylamide (DMAA): 3,160 mg/kg (rat, oral) |
| NIOSH | RN0160000 |
| PEL (Permissible) | PEL (Permissible Exposure Limit) for N,N-Dimethylacrylamide (DMAA) is not specifically established by OSHA. |
| REL (Recommended) | 10 mg/m³ |
| Related compounds | |
| Related compounds |
N,N-Dimethylformamide Acrylamide N-Methylacrylamide N,N-Diethylacrylamide N-Isopropylacrylamide Methacrylamide N,N-Dimethylmethacrylamide |
| Related compounds |
Acrylamide N-Methylacrylamide N,N-Diethylacrylamide N-Isopropylacrylamide N,N-Dimethylformamide N,N-Dimethylmethacrylamide |
