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HS Code |
964303 |
| Chemical Name | N,N'-Methylene Bisacrylamide |
| Cas Number | 110-26-9 |
| Molecular Formula | C7H10N2O2 |
| Molecular Weight | 154.17 g/mol |
| Appearance | White crystalline powder |
| Melting Point | 270-275°C (decomposition) |
| Solubility In Water | Soluble |
| Density | 1.235 g/cm³ |
| Purity | Typically ≥99% |
| Odor | Odorless |
| Ph 1 Solution | 6.0-8.0 |
| Storage Conditions | Keep tightly closed in a cool, dry place |
| Synonyms | MBA; Methylenebisacrylamide |
As an accredited N,N'-Methylene Bisacrylamide factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 100g N,N'-Methylene Bisacrylamide is packaged in a sealed, labeled, white HDPE bottle with a tamper-evident screw cap. |
| Shipping | N,N'-Methylene Bisacrylamide should be shipped in tightly sealed containers, away from light, heat, and moisture. It is typically transported as a solid, with appropriate hazard labeling. Handle with care, using gloves and eye protection. Follow all local, national, and international regulations for transporting chemicals classified as hazardous substances. |
| Storage | N,N'-Methylene Bisacrylamide should be stored in a tightly sealed container, in a cool, dry, well-ventilated area away from heat, light, and incompatible substances such as strong oxidizers. Avoid exposure to moisture and direct sunlight. Use dedicated storage space, labeled appropriately, and keep away from food or drink. Wear suitable protective equipment when handling to prevent contact or inhalation. |
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Purity 99.0%: N,N'-Methylene Bisacrylamide with purity 99.0% is used in polyacrylamide gel electrophoresis, where enhanced resolution and reproducibility of protein separation is achieved. Low viscosity: N,N'-Methylene Bisacrylamide with low viscosity is used in hydrogel synthesis, where it ensures uniform cross-linking and smooth gel formation. Particle size 100 mesh: N,N'-Methylene Bisacrylamide with particle size 100 mesh is used in biomedical scaffolds, where rapid dispersion and homogeneous distribution within polymer matrices are obtained. Melting point 150°C: N,N'-Methylene Bisacrylamide with melting point 150°C is used in thermal curing resins, where stable interlinking and high-temperature resistance are provided. Molecular weight 154.17 g/mol: N,N'-Methylene Bisacrylamide with molecular weight 154.17 g/mol is used in chromatography media, where precise pore size control for molecular separations is enabled. Stability temperature up to 80°C: N,N'-Methylene Bisacrylamide stable up to 80°C is used in aqueous polymerization reactions, where consistent cross-linking efficiency is maintained under moderate heat. High solubility in water: N,N'-Methylene Bisacrylamide with high solubility in water is used in contact lens manufacturing, where transparent and hydrophilic polymer networks are formed. Moisture content ≤0.5%: N,N'-Methylene Bisacrylamide with moisture content ≤0.5% is used in tissue engineering hydrogels, where extended shelf life and minimized hydrolysis risk are realized. Analytical grade: N,N'-Methylene Bisacrylamide of analytical grade is used in laboratory reagent preparations, where high purity and reliable analytical results are guaranteed. |
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N,N'-Methylene Bisacrylamide has found a unique place in lab work and industrial processes because of the way it helps build molecular structures. The chemical, known to many as MBAA or just “bis,” often shows up around research benches, where it makes a quiet impact on the routines of polymer science. After years of hands-on work with acrylic polymers and electrophoresis, it’s clear this compound tends to be less talked about compared to other ingredients, yet it holds a central role, quite literally linking everything together. Its model numbers—like MBAA-99 or MBAA-98, depending on the supplier—mainly reflect purity, which usually ranges from 98% to just above 99%.
What often sets MBAA apart is the twin acrylamide groups on either side of a methylene bridge. Those who have poured their share of polyacrylamide gels soon learn this bridge matters. The compound works as a crosslinker, meaning it connects acrylamide chains in three dimensions. When mixed with acrylamide and an initiator, MBAA helps form gels with pores large or small, all depending on how much gets added. More MBAA locks the network down tight; less gives it some give. This isn’t just chemical trivia. In protein electrophoresis, fine-tuning the MBAA ratio defines how well a gel can separate molecules by size. Pore size impacts more than just lab results. A good gel can mean the difference between seeing fuzzy bands and crisp, trustworthy data—something every researcher values.
Anyone who has opened a fresh batch knows MBAA as a white crystalline powder, sometimes showing off faint clumps if the container’s spent too long in humid air. Higher-grade MBAA stays powdery longer, and its purity matters. Impurities, even at the level of a fraction of a percent, start to creep into experimental results. For folks in industrial roles—those developing synthetic hydrogels for agriculture, water treatment, or drug delivery—consistency can mean better performance and less troubleshooting. In the lab, purity affects reactivity, so workers seek grades that minimize the background noise. Some research labs settle for 98% but clinical or pharmaceutical applications rely more on 99+%. Just as gourmet chefs prize their ingredients, chemists start to notice the little things when precision matters.
Specifications go past just numbers on purity—people want to know about solubility, melting point, and stability. MBAA dissolves well in water, which makes cleanup and prep simple but also means it picks up moisture if left carelessly sealed. Its melting point lands just above 150°C, but nobody wants to push it that far: MBAA starts to decompose before actually melting, which can release harmful vapors. Sensible handling and storage become everyday habits. Small things—like keeping the jar cool, dry, and allergy-aware—make for safer and more reliable results in the long haul.
Those with hands-on experience know MBAA first and foremost as a crosslinker for acrylamide gels. In biochemistry classrooms, some stumble through early attempts at pouring gels, learning firsthand the trade-off: too little MBAA and the slab falls apart, too much and proteins run slow or not at all. Experiment after experiment, the ratio of acrylamide to MBAA becomes a thing of preference and necessity. The numbers mean something—usually hovering from 19:1 or 29:1, depending on what’s being separated. Over time, users swear by their own blends and have good reasons for those habits.
Schools and hospitals rely on MBAA-polished gels to keep biomolecular research moving. The accuracy of disease markers, DNA fingerprints, and protein assays can hang on one ingredient behaving as expected. Even outside academic labs, its impact shows up: gel-based water treatment media rely on MBAA for their specific pore structure, needed to filter or hold contaminants. The same backbone, built from crosslinked acrylamide and MBAA, shows up in everything from absorbent diapers to the thin films in some wound dressings. What all these uses share is a need for matrices with just the right flexibility and strength.
Studying alternatives can highlight what makes MBAA different. Some crosslinkers—diamines or other bis-compounds—do the job, yet often change the chemistry in the process. MBAA links polymer chains by radical mechanisms, fitting neatly into acrylamide networks. Other options, like ethylene glycol dimethacrylate (EGDMA), lean toward use with different monomer systems, often favoring organic solvents and less water. Those who swap them out see a change in final gel properties: different crosslinkers lead to different swelling, elasticity, or pore size. One benefit of sticking with MBAA is its reliability in water-based systems. Once dialed in, the chemistry offers a predictability other options fight to match.
Cost comes into play as well. Some alternatives, though interesting, push budgets or bring more complicated handling needs. MBAA offers a cost-effective balance of reactivity and accessibility, which explains its near-universal presence in academic settings. Seen through the lens of experience, users who have tried “fancier” crosslinkers often circle back to MBAA for those classic protocols, mostly because the data compare well across decades and across labs.
Years spent in labs teach anyone that handling bisacrylamide demands focus. Like acrylamide itself, MBAA carries toxicity concerns, especially before polymerization. The powder can irritate eyes and skin, so gloves, goggles, and a fume hood are standard operating procedure. There’s no shortcut to safety: several regulatory bodies have flagged unpolymerized acrylamides as neurotoxic. Good ventilation and careful clean-up routines keep trouble at bay. Waste must go to the right channels—no washing down the drain or tossing with regular rubbish. Over time, these habits become second nature, a part of any responsible research operation.
Policies have shifted as the health data have refined. Years back, not everyone knew the risks, but experience and regulation have shaped safer cultures. Educators now spend more time teaching safe prep and disposal. Quality safety data sheets arrive with every shipment, and users pay attention. Product purity intersects with safety: less contamination means fewer unknowns in the workflow.
Disposal stands out as a long-term worry. Pre-polymerized MBAA, like acrylamide, can find its way into water or soil if handled carelessly. Modern labs have moved toward closed-systems and automated gel casting stations to limit exposure. In larger operations, vapor containment and specialty waste channels protect workers and the environment. The hydrogels that result, once formed, pose much less risk because the crosslinking locks up the reactive acrylamide units, but every operator ought to keep in mind the journey from powder to solid matters. Used gels don’t go to general waste bins. Properly marked, sealed containers end up headed to chemical waste processing plants.
Green chemistry trends push for innovative crosslinkers with better degradability and less toxicity. New research continues to look at safer gel chemistry for both people and wildlife. Valuable as MBAA is, the hunt for alternatives grows in importance, especially as large-scale industrial use climbs. Still, for many current applications, MBAA remains the go-to. It’s like the reliable tool in the box—familiar, predictable, and trusted—while the hunt for greener practices goes on.
Any stockroom technician will tell you: proper storage counts. MBAA keeps best in tightly sealed, moisture-proof containers, away from heat and sunlight. That white powder can clump if it draws moisture, making accurate weighing and mixing difficult. A desiccant pouch or even a resealable double bag adds a layer of insurance. For shelf life, MBAA holds up for a year or more when treated right. Old, yellowed MBAA often ends up on the hazardous waste path—another reason to avoid overordering.
Quality control often gets tested by experienced eyes. Long-term researchers develop a sense for the expected look and feel of a good sample. Unusual odors, clumping, or off-color powder often raise a red flag well before paperwork catches up. Reliable suppliers post batch data and lot-specific certificates, often vetted by internal quality teams or third-party labs. Sitting in the middle of a long supply chain, users push for stricter oversight, pressing back on even small consistency changes. This vigilance keeps lab results comparable year after year, across regions and research groups.
Those who’ve poured gallons of acrylamide solutions or spent weeks troubleshooting flawed gels know well how even small mistakes ripple out. A batch of MBAA exposed to humidity during storage can go lumpy, making it hard to weigh the right amount. If the dry powder clings to the scoop or container, you never quite know you’re mixing a repeatable batch. Sometimes, gels don’t set right, bands turn streaky, or proteins don’t run clean—an old, poorly stored bag of crosslinker ends up the hidden culprit.
Every lab hand has a story about “mystery bands” or gels that fall apart with just a touch. More often than not, these go back to expired reagents or ratios that got nudged off by a careless scoop. Keeping logs, double-checking weights, and knowing when a bottle is past its prime saves many hours down the road. Over time, researchers trust themselves to sniff out subtle changes in reagent quality even before the instruments do. These skills don’t come from manuals—they grow from doing, watching, and learning from mistakes.
One trick passed between technicians involves preparing a small test gel with each new batch: if the standard markers run true, the lot passes muster. If not, it’s back to basics. Lessons like these underline how MBAA’s performance hinges on care at every step. Less experienced researchers might blame their pipettes or protocols. Veteran hands look to their chemicals and aren’t afraid to toss a questionable batch.
Maintaining reliability with MBAA involves more than just following a recipe. Labs that run smoothly lean on well-established routines: ordering the right grade for the job, recording storage dates, labeling opened bottles, and watching for signs of aging. Training plays a huge role. Whether onboarding new techs or retraining seasoned pros after a lapse, the work pays off when experiments perform as promised.
For institutions, spending a moderate amount more on high-quality MBAA avoids wasted hours and money on troubleshooting. Some suppliers offer custom pack sizes—those orders help reduce waste and keep reagents fresh. Larger projects might set up automated gel-casting workstations, keeping MBAA exposure down while increasing throughput and reproducibility.
Cross-department sharing of successful protocols helps, too. Labs post their best ratios, not just for the record, but for the next user looking to avoid invented pitfalls. Documentation of wins and losses builds not just trust in the outcome but confidence in the method. Some teams even rotate responsibility for reagent prep, building familiarity and redundancy—lowering the odds that a weak link in the chain throws off a semester’s work.
Industry has picked up on MBAA’s flexibility and reliability. Makers of contact lenses, hygiene products, soil conditioners, and medical dressings depend on the stable, predictable crosslinks MBAA creates. The same physical principles learned in the lab—how much crosslinker to use, how it changes the final product’s toughness or water uptake—carry through to scaled-up production lines.
Farm sectors that use hydrogel-based water-retaining agents for drought-prone soils rely on MBAA crosslinks for predictable swelling. Water treatment plants use polyacrylamide gels to trap contaminants. Medical tech companies produce wound dressings that must hold together under pressure while letting in moist air. All of these industries learn, often the hard way, that cutting corners with MBAA purity or storage shortens product shelf life and increases risk of failure in the field. Periodic quality sweeps, not just of the product but of incoming shipments, protect the entire line. Consumers, rightly, expect high performance—something that starts with good choices at the chemical stockroom.
Sustainability weighs heavy on the field these days. Some chemists look for “greener” crosslinkers—modified polysaccharides, polyvinyl alcohol blends, or naturally derived materials. Each brings its own tradeoffs. Some lack the same mechanical strength, others cost far more. Polysaccharide-based gels decompose safely and draw less regulatory attention, though often at the price of performance in harsh conditions.
Efforts to cut down on acrylamide and MBAA exposure continue apace. Automated mixing stations, sealed reagent kits, and pre-cast gels cut down on worker exposure. Manufacturing plants move toward closed-loop water handling and solvent containment. While complete replacement of MBAA remains a longer-term goal, incremental improvements in procedure and training are making day-to-day work with this chemical safer and a bit more sustainable.
What stands out most after years working with MBAA is the balance it offers. The reliability, the way results align with the literature, the predictability of the chemistry—it all removes variables, letting researchers focus on their science. Comparisons against the growing library of alternatives highlight its effectiveness, especially in tough, high-specificity lab situations.
The simplicity of MBAA’s action—two acrylamide groups on a single bridge—means chemists can model its effects, predict its limitations, and communicate results across borders and decades. While critics point out toxicity risks, the experience-driven precautions help avoid incidents. Researchers who have worked through cycles of improvement, training, and policy changes develop real trust in MBAA’s role, even as they stay open to new innovations and safer replacements. The story of this crosslinker, from student bench to industrial reactor, shows both the power and the challenge of balancing performance and responsibility in modern chemistry.
The next years will likely see new crosslinkers pushing past MBAA in certain areas, maybe relying less on petrochemicals or creating safer, biodegradable backbones. Institutions have started including sustainability criteria among their purchasing guidelines, and researchers enter the field with a sharper awareness of health, water, and waste issues. MBAA still stands as the tested benchmark, the ingredient against which new polymers get measured.
Success stories and failures both steer the field forward. One day, an entirely new standard may emerge, but for now, MBAA links decades of research, serves industries, and keeps labs connected to a deep tradition of reproducible science. The work with this chemical may never make headlines, but for those in the trenches, it’s a quietly pivotal substance—one that shapes both the expected and the yet-to-be-discovered in the world of polymers.