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1,3-Butanediol Diacrylate: Insight into a Versatile Acrylate Monomer

Historical Development

Chemists started exploring ways to modify basic molecules for industrial use back in the early to mid-20th century. The push for flexible, durable polymers created a need for new diacrylate monomers. 1,3-Butanediol diacrylate came about during a period when companies and research labs eagerly sought alternatives to classic materials, especially those with high performance under stress. The molecule fell right into this era of innovation—mainly due to its two acrylate groups and the backbone flexibility imparted by the 1,3-butanediol core. Over the decades, rising demand from adhesives, coatings, and plastics industries helped cement its place in specialty chemical catalogs.

Product Overview

1,3-Butanediol diacrylate offers two reactive acrylate sites tied to a four-carbon chain. This setup delivers more flexibility and impact resistance to a finished polymer than short, stiff linkers. Many suppliers pack it in drums or totes, labeling it for resin and crosslinking use. The diacrylate’s performance benefits include its low viscosity and its rapid curing under UV or electron beam, making it a favorite for light-cured adhesives, inks, and paints. For makers of 3D printing resins or protective topcoats, its unique blend of strength and flexibility spells trouble for older materials struggling to keep up.

Physical & Chemical Properties

This liquid holds a faint, ester-like smell and a colorless to pale yellow appearance. It’s got a density close to 1.03 g/cm³ at room temperature, so it pours smoothly but won't evaporate too fast. It doesn’t boil easily, breaking down before traditional boiling even kicks off, which means you handle it more like a resin than a solvent. Mixes with other acrylates and common solvents without complaint. It stays away from water and doesn’t like open air—exposure makes it polymerize in clumps or films due to those hungry double bonds. Its flash point sits high enough to discourage worry, but people in a lab or factory don't let their guard down.

Technical Specifications & Labeling

Commercial shipments usually carry a minimum purity spec above 95%. Labels show the CAS number 3139-05-7, with stabilizers such as hydroquinone monomethyl ether getting listed in trace amounts to keep things from gelling during transport. Viscosity hovers between 8 and 15 mPa·s at 25°C, which tells coating formulators what sort of flow to expect. In practice, buyers want stable peroxide numbers and clear, impurity-free material. Makers test acidity carefully because small acid build up triggers early gelation. SDS and TDS sheets always come with the drums, laying out PPE, flammability data, and recommended temperature controls during storage.

Preparation Method

Manufacturers typically produce 1,3-butanediol diacrylate using esterification. They combine purified 1,3-butanediol with acrylic acid, usually under nitrogen to block out oxygen. Mix in an acid catalyst—companies stay loyal to sulfuric acid or p-toluenesulfonic acid—and manage heat to coax along the reaction. Water gets sucked out, sometimes in a Dean-Stark trap, until the shift to the diacrylate reaches a stable conversion. After the reaction, washing and vacuum distillation remove acids and leftover acrylate for a product that pours out clean and almost colorless. The addition of polymerization inhibitors staves off any early setting in barrels or pipelines.

Chemical Reactions & Modifications

This molecule welcomes radical polymerization, especially under UV. Each acrylate group reaches out to nearby monomers, locking down dense, crosslinked polymers fast. Add in photoinitiators or peroxide compounds, and you've got a setup that creates structural resins in minutes. Some custom syntheses graft functional molecules onto it or replace a chunk of one acrylate group to tweak flexibility or add hydrophilic branches. Formulators love switching between straight diacrylate, partial esters, or copolymer blends to hit sweet spots for adhesion or toughness. The structure leaves plenty of room for clever side reactions, and that keeps lab folks busy developing new coatings and composites.

Synonyms & Product Names

Chemists know 1,3-butanediol diacrylate by several names: BDDA, 1,3-butanediol, diacrylate, or butylene glycol diacrylate show up in catalogs. Some suppliers market it as Ebecryl 140 or similar trade names aimed at resin makers. The CAS number—3139-05-7—remains a trusted identifier across borders and languages, offering a clear shot through any confusion in a crowded SDS database.

Safety & Operational Standards

Workers handle BDDA with gloves and goggles. In my own time working with acrylates, nobody wanted any of it on skin—prolonged contact leads to burning or dermatitis. Fume hoods run whenever open vessels are involved, because vapors can irritate eyes and lungs. Spills need careful cleanup, since uncured liquid gets sticky and makes a mess that’s tough to scrub out of floors or gear. Safety Data Sheets stress the need to store it out of sunlight and away from acids, bases, or radical initiators. In larger shops, storage drums sit in well-ventilated, temperature-regulated spaces that keep everything dry and hazard labels facing forward.

Application Area

In printing and electronics, BDDA delivers flexibility and fast cure that help printed circuits hold their shape under stress. Dental and medical compounders value its low shrinkage during curing—nobody wants a brittle retainer. Paint and coating folks mix it into UV-curing lacquers for wood floors and automotive parts, counting on its impact resistance. Some industries leverage its use in fiber optics and adhesives, especially where long-term clarity and strength cut down on warranty headaches.

Research & Development

R&D teams keep pushing boundaries by testing BDDA copolymers that balance flexibility with heat resistance for newer, more sustainable applications. Over the years, companies blend BDDA with renewable monomers and search for less toxic photoinitiators—not only to cut emissions but to keep their supply chain healthier. In one of my early research projects, blending BDDA with bio-based diols led to a new batch of eco-resins suitable for green packaging and compostable coatings. Nobody wants to stick with a 50-year-old recipe, so even conservative industries keep tabs on lab reports for new ways to mold, print, or cure with this monomer.

Toxicity Research

Long-term studies show BDDA causes irritation on contact, but keeps off the lists of worst offenders for organ toxicity compared to some older acrylates. Still, repeated exposure in unprotected settings raises risks of allergies, especially for handlers. Toxicologists conducted tests that suggest minimal vapor inhalation risk under normal factory conditions, but accidental spills or fires release acrylate fumes that demand swift evacuation. Industry standards keep exposure limits tight and recommend constant ventilation and regular skin checks for workers. Following strict waste disposal routines remains the cleanest way to manage leftover product and protect air and water around plants.

Future Prospects

Expect use of 1,3-butanediol diacrylate to shift as industries chase greener, smarter materials. Labs continue developing copolymers that rely less on fossil-based acrylates by modifying the starting diols. Electronics and automotive sectors push for resins combining flexibility and high-performance, nudging research toward BDDA’s strengths. Some regulators look harder at any acrylates in workplace air or wastewater, fueling a move to safer production or end-of-life recycling. As additive manufacturing and advanced medical devices grow, BDDA remains a molecule researchers return to, because thorough chemistry and real-world toughness rarely fall out of style.



What is 1,3-Butanediol Diacrylate used for?

Getting to Know 1,3-Butanediol Diacrylate

Chemistry class never gave most people a reason to remember compounds like 1,3-Butanediol Diacrylate, but this colorless liquid shows up in more corners of our lives than we think. Most of its work happens behind the scenes, in places like manufacturing floors and laboratories. Having spent a stint working at a plant that made specialty coatings, I learned that this chemical earns its keep by lending strength and staying power to all kinds of products.

Resins, Coatings, and Everyday Strength

Manufacturers like 1,3-Butanediol Diacrylate for making tough, long-lasting materials. Toss it into an acrylate resin and you get something that stands up to scratches and sunlight. The molecule packs two acrylate groups, which means it forms sturdy connections with other chemicals. Paint makers want that kind of cross-linking because it keeps floors and countertops looking fresh even after years of wear. Dental labs use it for the same reason, pulling it into fake teeth or fillings that must resist chewing and chipping.

In printing, it adds crisp definition to inks and printer plates. I’ve met folks who work in 3D printing, and they swear by acrylate-based resins that cure quickly under UV light. Without sturdy monomers like this one, hobbyists and commercial printers would see prints that crumble or fade too soon.

Electronics Are Built to Last with It

Gadgets clog our world, and inside most cases you’ll find parts sealed up with tough synthetics. Circuit boards, for example, sit inside layers of cured resin to keep out water and dust. The ability of 1,3-Butanediol Diacrylate to link up with other chemicals at room temperature means electronic manufacturers keep assembly lines moving without long wait times for glues to cure.

Without these fast-curing and resilient adhesives, makers of smartphones, solar panels, and circuit breakers would spend more time and money fixing cracked or unreliable units than actually building new ones.

Health, Safety, and Environmental Concerns

Chasing durability comes with responsibility. Acrylates, including 1,3-Butanediol Diacrylate, create fumes during processing that can irritate lungs and skin. I still remember the strict controls at my old job: masks, gloves, and big exhaust fans running all day. Workers report skin allergies when exposed too often without protection, and spills can threaten water sources.

Research from the European Chemicals Agency suggests that proper handling cuts the risks way down. Following rules and switching to processes with less exposure lower the odds of someone getting sick. Companies also focus more on recycling waste and choosing greener methods, though complete safety relies on honest enforcement and regular oversight.

A Path Towards Smarter Use

As new materials push for greener, healthier chemistry, companies are experimenting with plant-based alternatives that do a similar job. Some universities test biosourced acrylates, hoping to keep performance but avoid some of the headaches from traditional petrochemicals. In my view, the future depends on real partnerships between workers, engineers, and regulators—not just profit margins. When everyone at a factory can breathe easy and still deliver products that last, the formula finally works.

What are the safety precautions when handling 1,3-Butanediol Diacrylate?

Understanding the Risks

Anyone who’s worked in a lab or manufacturing floor knows those sharp chemical smells and strong warnings aren’t just for show. 1,3-Butanediol diacrylate brings a few challenges to the table, mixing skin, eye, and respiratory hazards with environmental concerns. Accidentally spilling it on bare skin or getting it in the eyes, even for a moment, can trigger a nasty reaction. Breathing in the vapors or missing an airborne splash could mean burns or irritation. It’s one of those chemicals that doesn't forgive a mistake.

Pay Attention to Personal Protective Equipment

I’ve learned to never underestimate simple gear. A chemical splash in the face once, several years ago, taught me to never skip goggles. For this chemical, don’t just reach for those thin disposable gloves—choose ones rated against acrylates, like nitrile or neoprene. Long sleeves and lab coats cut down on exposed skin, and a decent set of chemical-resistant goggles keeps your eyes clear. In places where splashing could happen, face shields build an extra barrier. Simple acts—double-checking your gloves, washing up right after handling, never eating or drinking near your workbench—go a long way.

Focus on Ventilation and Containment

The importance of fresh air can’t be overstated. If there’s even a hint of vapor when cracking open a bottle, it means the fumes need controlling. Fume hoods or well-designed ventilation systems reduce the risk of irritation or worse. When storing the chemical, keep containers sealed up tight and mark them clearly. Accidents often happen during transfer, so use secondary containers and spill trays. It’s not just about personal safety—these steps protect colleagues and even cleaning staff, who often get overlooked.

Preparation for Spills and Exposure

An emergency eyewash that’s actually tested and clear of clutter matters far more than you think—especially if you ever need it. Know exactly where it sits in the room. Keep neutralizing agents and spill kits nearby. Absorbent pads and proper waste containers prevent an accidental spill from turning into a major event. If contact occurs, flushing with water for a full fifteen minutes sounds like a small eternity, but it can make all the difference. Reporting any accident, even a near-miss, helps curb future risks and creates a stronger safety culture.

Disposal Doesn’t End at the Sink

Once, I saw a new lab worker rinse leftover acrylate straight down the sink. Greener, safer chemistry practices now rank higher than blind convenience. Acrylates can damage water sources and harm aquatic life, so collecting all waste in proper containers and labeling them for hazardous waste pickup protects communities beyond the lab. Quick “out of sight, out of mind” shortcuts almost always come back around—sometimes in fines, sometimes in lost reputation.

Commit to Training and Staying Alert

Complacency shows up just when you think you know everything about your chemical shelf. Annual training isn’t a check-the-box chore—it refreshes muscle memory and teaches about any updated hazards. Reading the material safety data sheet before handling something new, asking questions, and double-checking procedures breaks up the routine and keeps everyone sharper. Working with hazardous chemicals—1,3-Butanediol diacrylate included—relies on more than book knowledge. It leans on habits, shared stories, and lessons learned from those who’ve been there before.

What is the chemical structure and properties of 1,3-Butanediol Diacrylate?

Chemical Structure That Leaves Its Mark

1,3-Butanediol diacrylate—just saying it out loud already hints at a mouthful, but the structure itself stays pretty straight: a four-carbon backbone, hydroxyls at both ends made into acrylate esters. The official formula looks like C10H14O4. What you get here is not some convoluted lattice—this is a chemical with clear handles for further reactions. The two acrylate groups stick out from each end of the butanediol core, like arms ready to grab. That feature supplies outstanding reactivity, something industries latch onto for making tough-as-nails polymers.

Properties That Shape Everyday Products

Let’s talk about what really puts 1,3-butanediol diacrylate in motion: its properties. It pours out as a clear, colorless, sometimes faintly yellowish liquid, with a slight acrid odor if you get too close. Low viscosity translates to easy mixing and handling. At room temperature, it stays stable, but under ultraviolet light or heat, it cures quickly—those acrylate groups spring into crosslinking, forming hardy networks. This ability to go from liquid to tough polymer brings it right into paints and coatings.

Aside from toughness, the final product takes on chemical resistance. Battery casings, circuit boards, dental applications—acrylates like this one show up in places where a fragile polymer would fail. The refractive index sits at about 1.45 and the boiling point hits over 250°C, keeping the molecule from breaking down easily during industrial processes.

Why 1,3-Butanediol Diacrylate Counts: From Labs to Real Life

Polymer scientists like having flexible building blocks at their disposal. In my hands-on experience with UV-cured inks, using 1,3-butanediol diacrylate felt a bit like adding superglue into the mix—a little bit radically changes the hardness and stickiness of a surface. Think about sports gear, kitchen countertops, or packaging that resists water and scratches. If you check the ingredient list on a long-lasting adhesive, an acrylate like this sits near the top.

There’s a catch. Acrylates come with health and safety baggage. Skin contact can irritate, even cause sensitization. The reactivity helping product quality also calls for careful storage; exposure to light or heat could trigger polymerization too early. In my lab days, we kept these bottles wrapped tight and away from any light. At scale, proper ventilation, gloves, and training aren’t just optional—overexposure to vapors builds up and causes problems with headaches or worse.

Finding Responsible Uses and Solutions

Industrial use of acrylates grows steadily, which begs the question: how to keep people and the environment safe? Regulatory measures in Europe and North America keep an eye on limits for workplace exposure. Biodegradability solutions lag behind preferences for these hard polymers. I’ve seen promising projects looking to replace petroleum-based butanediol with bio-based sources, which could trim down the fossil footprint. Also, innovations in closed-loop systems for handling and curing minimize waste.

Still, switching to alternatives isn’t so easy. For now, best practices rely on smart storage, rigorous handling routines, and up-to-date training so the benefits don’t get overshadowed by hazards. Consulting material safety data sheets becomes routine, and companies seek suppliers with strong reputations for environmental stewardship. Science keeps hunting for that balance—robust materials, healthy workplaces, and less environmental drag.

How should 1,3-Butanediol Diacrylate be stored?

Getting Real about Chemical Storage

If you’ve ever spent time around a resin or adhesives factory, the tang of acrylates becomes familiar. 1,3-Butanediol diacrylate, with its role in specialty coatings and 3D printing resins, brings a different set of worries. Storage is less about just following the rules—it's about keeping folks safe and keeping the budgets tight by avoiding leaks or spoilage. I remember hearing about a rushed shipment that spent too long baking in a summer sun; that day nobody wanted to talk about the cost of waste. So, how do you keep this stuff in line? Start from basics, but don’t ignore the details.

Why Temperature and Light Matter

Heat sneaks up in a busy warehouse. Most acrylates break down if left in the wrong spot for days. 1,3-Butanediol diacrylate can polymerize from sun exposure or high temperatures—and that's when the headaches start. Clumping, hardening, ruined barrels. Quality sinks, production halts, and the accounts team finds a new gray hair or two. Historically, smart facilities store this chemical below 30°C, away from direct light and definitely not beside a space heater. Some shops tuck the drums into insulated rooms or even refrigerate smaller batches destined for research.

Keep Moisture and Air in Check

Humidity brings its own drama. 1,3-Butanediol diacrylate absorbs water from the air, which triggers unwanted reactions and can throw off the science behind high-end coatings or adhesives. Leaky containers don’t just lose product—they risk gumming up safety gear or feeding a mold bloom. Making sure containers seal tightly, and keeping desiccant packs on the shelf, blocks much of this trouble. Open a drum for a sample, and close it right away, even if you plan to use the rest later that week.

Use the Right Containers

Metal drums with inner liners, high-grade plastics, and robust seals often offer the best defense. Not every container will work. Just last year, a local tech startup lost two thousand dollars’ worth of material using thin wall jugs. Over time, 1,3-Butanediol diacrylate creeps through cheap packaging, or worse, reacts with bare metal. Investment in proper containers may sting your quarterly costs, but you only make that mistake once.

Think Fire and Chemical Safety

This is not water off a duck’s back; acrylates are flammable. Local codes demand storage away from ignition sources, and for good reason. Even a poorly-wired forklift can spell disaster. Signage, fire extinguishers, and grounding straps are not red tape—they’re the reason insurance premiums stay reasonable and staff go home safe. I’ve supervised safety drills, and almost every run proves the point: preparation beats panic.

Handling Spills and Waste

Mistakes happen—somebody bumps a stack, the valve sticks open half a turn, and now there’s acrylate on the floor. Having spill kits with absorbent pads, personal protective gear, and a clear map of exit routes isn’t optional. Fill waste drums promptly and move them to the right disposal point by the end of the shift. Skipping this step invites cross-contamination and surprise inspections that never end with a handshake.

Staff Training Makes the Difference

Fancy gear and detailed plans fall short without a crew who understand why these steps aren’t negotiable. In my experience, regular walk-throughs and open conversations about chemical risks do more to prevent problems than lectures or printed manuals. It’s about consistent habits, not just compliance checklists.

Is 1,3-Butanediol Diacrylate hazardous to health or the environment?

Digging Into the Risks

The name 1,3-Butanediol Diacrylate sounds clinical, but the reality around it leaves no room for formality. This chemical shows up in resins that companies use for coatings, adhesives, and inks. People ask if it brings health or environmental trouble with it. The answer doesn’t come with yes or no, but with facts worth unpacking.

Breathe in a whiff of this substance in a setting that skips proper ventilation, and the body responds. Eyes burn, throats itch, and headaches aren’t far behind. This isn’t a mystery. Decades of workplace health studies point out skin irritation and a higher risk for workers who skip gloves. Allergic skin reactions show up, and the risk isn’t just paperwork hype; plenty of cases land in occupational health research journals. Authorities like the European Chemicals Agency flag it as a skin sensitizer, which places a real onus on users to respect safety protocols.

Long-Term Exposure Can Sneak Up

Casual handling might not bring instant collapse. The real test comes over time. Repeated exposure often brings more than mild irritation. Workers downwind face chronic dermatitis. Experience on factory floors shows that ignoring those small signs leads to days out of work, tough medical bills, and grim discomfort nobody needs.

Respiratory symptoms cannot be swept under the rug. Acrylic-based chemicals like 1,3-Butanediol Diacrylate have a history of causing asthma-like symptoms when inhaled. The pain is real, especially for folks already dealing with allergies or asthma.

What About the Environment?

Chemicals do not vanish down the drain. Water treatment facilities work hard, but they don’t erase every trace. Spill this acrylate-based substance into soil or water, and wildlife pays the toll. Reports from environmental monitoring groups have shown impaired aquatic life when runoff contains reactive acrylates. Fish and invertebrates in affected streams develop problems, sometimes even at low concentrations. The reaction with sunlight makes some acrylates more toxic in water, compounding the risk. This is more than hypothetical: cases in industrial zones across Europe and North America underline the pattern.

Fact-based Responsibility Beats Guesswork

I spent summers working near industrial plants, where unexpected headaches and rashes turned out to be linked to careless chemical handling. Companies that took strict steps to control air where workers moved, provided real training, and switched to less harmful alternatives saw healthier, happier workforces.

Regulators push for substitution—replacing 1,3-Butanediol Diacrylate with safer monomers where possible. Where the swap can’t happen, personal protective equipment gives workers a lifeline. Gloves, face shields, and even local exhaust systems crush risks before they turn into health crises. Training sits at ground zero. People who know what they’re working with make fewer mistakes and catch leaks faster. Frequent monitoring of workplace air and runoff water helps spot trouble early, making problems more manageable.

Tools for tracking spills and managing waste have improved. Companies that keep a tight watch on chemical storage and waste response see fewer incidents. Simple steps—tight lids, regular inspections, and prompt spill cleanups—often prove cheapest in the long run.

Workers, safety staff, environmentalists: each has a stake. Pushing for safer processes, new research, and candid reporting changes the story of chemicals like 1,3-Butanediol Diacrylate from one of hidden danger to accountable growth. At the end of the day, protecting people and planet isn’t red tape—it’s common sense backed by experience and evidence.

1,3-Butanediol Diacrylate