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HS Code |
380398 |
| Chemicalname | Crotonaldehyde |
| Casnumber | 123-73-9 |
| Molecularformula | C4H6O |
| Molarmass | 70.09 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Odor | Pungent, suffocating |
| Boilingpoint | 104°C (219°F) |
| Meltingpoint | -76°C (-105°F) |
| Density | 0.846 g/cm3 at 20°C |
| Solubilityinwater | Miscible |
| Flashpoint | 21°C (70°F) |
| Refractiveindex | 1.4177 at 20°C |
As an accredited Crotonaldehyde factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle labeled "Crotonaldehyde, 500 mL," with hazard warnings, tightly sealed cap, and chemical identification and handling instructions. |
| Shipping | Crotonaldehyde should be shipped in tightly sealed containers, away from heat, flames, and incompatible materials such as strong oxidizers. It is classified as a flammable liquid and toxic substance; therefore, shipping must comply with relevant regulations, using appropriate labeling and packaging to prevent leaks, spills, and exposure during transport. |
| Storage | Crotonaldehyde should be stored in a tightly closed, well-sealed container in a cool, dry, and well-ventilated area, away from direct sunlight and sources of ignition. It should be isolated from strong oxidizers, acids, and bases. The storage area must be equipped with proper spill containment and clearly labeled. Avoid contact with incompatible materials to prevent hazardous reactions. |
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Purity 99%: Crotonaldehyde with purity 99% is used in pharmaceutical intermediate synthesis, where it ensures high yield and reduced impurity formation. Boiling Point 104°C: Crotonaldehyde with a boiling point of 104°C is used in agrochemical manufacturing, where its volatility allows efficient removal during downstream processing. Stability Temperature 30°C: Crotonaldehyde with a stability temperature of 30°C is used in resin production, where thermal stability minimizes product degradation. Molecular Weight 70.09 g/mol: Crotonaldehyde with molecular weight 70.09 g/mol is used in flavor and fragrance formulation, where precise molecular mass supports consistent aroma profiles. Reactivity Index High: Crotonaldehyde with high reactivity index is used in coating additive development, where rapid polymerization improves curing times. Viscosity 0.35 mPa·s: Crotonaldehyde with viscosity 0.35 mPa·s is used in rubber accelerator synthesis, where low viscosity facilitates homogeneous mixing. Water Content <0.2%: Crotonaldehyde with water content below 0.2% is used in specialty chemical manufacturing, where low moisture prevents side reactions and improves product stability. Storage Stability 12 Months: Crotonaldehyde with storage stability of 12 months is used in industrial adhesive production, where long-term shelf life assures supply reliability. Color APHA ≤15: Crotonaldehyde with APHA color ≤15 is used in dye precursor processes, where low color index ensures product purity and minimizes discoloration. |
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Most people stroll past the word "Crotonaldehyde" and never give it a thought. I didn’t until I found myself knee-deep in an old factory’s records, tracing the roots of its chemistry. Crotonaldehyde, with the formula C4H6O, comes as a clear, pungent liquid that has quietly carved out a place in countless industrial processes. It may not be a household name, but its fingerprints are on everything from leather to rubber and fuel additives. Its model—sometimes called trans-crotonaldehyde, or simply trans-2-butenal—carries a carbon backbone that encourages all sorts of chemical transformations, making it a versatile little molecule.
Specifications matter in this field. Industrial-grade Crotonaldehyde usually comes with a purity above 98%. Density hovers close to 0.85 g/cm³ at room temperature and it shows a boiling point just over 100°C. Handling this substance in small batch manufacturing has given me a deep respect for its reactivity—and for workers' safety. Anyone who’s worked with it recognizes its sharp scent immediately, so it’s impossible to ignore proper ventilation.
Crotonaldehyde works hard behind the scenes. Its main job is as a chemical intermediate—a raw ingredient that helps manufacturers build more complex compounds. It’s like clay for chemists. In my own career, I've watched Crotonaldehyde tie industries together: a batch leaves a chemical plant, heads to a flavoring company, and reemerges in the scent of artificial vanilla or the taste of butter flavor. The same batch, from another supplier, heads off for a run in pharmaceuticals, helping make drugs to treat infections or reduce pain.
One area where Crotonaldehyde cannot be overlooked is the field of synthetic rubber. By reacting with formaldehyde or other aldehydes, it builds polymers that make tires and hoses more flexible, more resistant to wear and tear. Automotive factories count on that kind of reliability. Leather tannery workers, too, benefit from its ability to cross-link protein chains, resulting in leather that’s tougher and less likely to crack. Even some pesticide and herbicide formulations draw from crotonaldehyde's toolkit.
These diverse uses are possible because Crotonaldehyde brings both reactivity and selectivity—it reacts eagerly with nucleophiles, forming new bonds, but its structure allows manufacturers to steer its behavior. I learned this firsthand when a pricing error sent the wrong isomer to our plant, which is how I discovered that the trans-form worked just right, while the cis-form hardly reacted at all in our setup. This sort of real-world experience gives me a sense of respect for chemists who pioneer new methods with such quirky molecules.
Comparisons help shine a spotlight on Crotonaldehyde’s value. Take acetaldehyde, a close cousin, which is more volatile and pops up in alcoholic fermentation. Unlike acetaldehyde, Crotonaldehyde sticks around longer in industrial processes, since its conjugated double bond offers extra stability. It resists vaporization and doesn’t lose potency when exposed to standard conditions—a huge benefit for anyone running a multi-step chemical synthesis in a large plant. Benzaldehyde, another common aldehyde, smells like almonds and flavors colas, but its aromatic structure won’t let it engage in the same range of chemical reactions. In my time formulating adhesives for bookbinding, Crotonaldehyde always won out over other contenders because it provided better cross-linking with less byproduct waste.
Most importantly, Crotonaldehyde’s structure allows it to serve as a bridge for adding other functional groups. Acetaldehyde can’t pull off the same diversity of reactions, and benzaldehyde tends to get locked into its aromatic cycles. Anyone who has tried to design a coating agent that must last in sun, rain, and chemical exposure will know how valuable that flexibility is. Back in the lab, we ran pilot projects replacing Crotonaldehyde with other intermediates. The results always came up short: coatings either failed in UV light or peeled away under stress. Switching back to Crotonaldehyde restored the product integrity.
Chemical factories have long faced tough safety questions with Crotonaldehyde. Its sharp, irritating smell hints at its power. Prolonged exposure in confined spaces can damage skin and lungs, so keeping ventilation systems maintained is never just a bureaucratic box to tick. I’ve seen shifts split up work in short bursts instead of one long session—it makes a visible difference in worker well-being. Modern regulatory standards set exposure limits that keep people safe. The Occupational Safety and Health Administration (OSHA) and comparable bodies abroad put Crotonaldehyde in a class requiring gloves, goggles, and regular air quality checks.
On the environment front, Crotonaldehyde breaks down in air and water over time, but its toxicity to aquatic life means spills are non-starters. Cleanups, as anyone in the field can confirm, require fast action and careful monitoring. The industry’s decades-long move to closed systems—where the chemicals stay inside pipes from start to finish—reflects this hard-earned wisdom. Newer plants often feature double-walled containment and infrared leak detection specifically because of accidents in decades past.
Finding safer alternatives has always been on my radar. Not every application can swap Crotonaldehyde out: for leather finishing, alternative cross-linkers cost more and sometimes don’t hold up. Still, the push for ‘greener’ chemistry is real, and some startups are working on plant-based intermediates that mimic Crotonaldehyde's strengths but break down faster in the environment. As these new molecules roll out from the pilot phase, it’s worth watching.
Innovation often starts with a question: what could Crotonaldehyde do if we saw it not just as a commodity but as a building block for new materials? For me, it became clear while consulting with a team trying to create bio-based adhesives. They needed a molecule to link together sugars into a tough yet biodegradable plastic. Crotonaldehyde stepped into this role and the resulting bioplastic showed both durability and ease of disposal—perfect for single-use packaging, without the legacy of waste.
Fuel additive developers take Crotonaldehyde’s reactivity and use it to form anti-knock compounds. These boosters help gasoline burn more smoothly, reducing both engine wear and emissions. Here, Crotonaldehyde offers an edge over simpler aldehydes, thanks to its double bond and ability to reinforce molecular chains under extreme engine conditions. Research in this area hasn’t stopped: I met mechanical engineers working on next-generation engines who test fouling and breakdown, and they found Crotonaldehyde-based additives kept combustion chambers cleaner over longer cycles.
Pharmaceutical companies, too, have turned to Crotonaldehyde in synthesizing key components for antivirals and antibiotics. Its structure allows fine-tuning of intermediate drugs—helping ensure a reaction doesn’t stall out midway. In my conversations with pharmaceutical chemists, many point out Crotonaldehyde saved months off development schedules thanks to its predictable performance, especially where higher-molecular-weight intermediates stumbled.
If you trace Crotonaldehyde’s role across decades, you’ll see how it’s followed the arc of industrial progress—always adapting, always squeezed for new advantages. Years ago, Crotonaldehyde came from crude distillation, piggybacking off the butanol and furfural trade. Equipment was simple, volumes were small, and by today’s standards the output was uneven. Now, large plants use continuous reactors and in-line testing, cranking out tons of consistent product. For a time, I worked in a facility rolling out these new reactors. Output shot up, waste dropped, and the environment inside the plant became noticeably safer.
Yet, tradition lingers: small-batch operations in leathercraft or specialty chemicals prefer the hands-on approach. They care less about scale and more about control over reactivity. Sometimes, it’s the local tannery that best appreciates Crotonaldehyde’s knack for customizing surface finishes and textures, rather than the mega-factory chasing economies of scale. My own trips to small-scale plants taught me to respect their detail-oriented approach, even if the global conversation is about bulk production.
While Crotonaldehyde brings clear benefits, no one in the industry ignores its risks. During my years troubleshooting plant operations, I encountered a recurring problem: people underestimating just how quickly this colorless liquid can irritate eyes, skin, and lungs. Even minimal leaks create air quality problems. After one incident, our plant updated equipment seals and rolled out emergency drills, which helped catch future leaks early.
Waste remains a sore spot. Crotonaldehyde’s high reactivity means any unintended release kicks off side reactions. Those byproducts are hard to treat. Our facility moved to smaller, sealed transfer lines and real-time analytics to keep byproduct levels down. It’s not a perfect solution, but it beats relying on manual checks. Some companies have set up on-site treatment stations, neutralizing Crotonaldehyde using hydrogen peroxide or potassium permanganate before sending water back to municipal systems. These extra layers of handling increase overhead, which makes it tempting for some to cut corners—an old problem that regulators address through surprise audits and hefty penalties.
Regulation has forced the hand of industry leaders. Europe’s REACH framework and the US EPA’s restrictions encourage substitution with safer intermediates. In regions with less oversight, knockoff producers sometimes dump residues, which hurts both local ecosystems and global reputation. The best-run companies see sustainability as a badge worth wearing and invest in community outreach programs, sharing air and water testing data with towns near their facilities. Experiences in these communities have convinced me that open communication is the only real way to build trust, especially where generations have lived alongside chemical plants.
No chemical, no matter how well understood, works by itself. People run the processes, respond to emergencies, and innovate new uses. In all my time with Crotonaldehyde—from research labs to busy plants—I’ve seen how much depends on human skills. The newest automated reactors don’t replace a seasoned operator who catches the faintest change in odor or color. Constant training helps, but so does building a workplace where workers feel they can speak up about strange readings or odd symptoms. Plant managers who make reporting easy, not scary, end up with safer environments.
Sharing expertise also extends outside the plant gates. At several industry conferences, panels on Crotonaldehyde often fill up fast. Newcomers want to learn how to calibrate detectors or swap stories about close calls and clever solutions. Here, experienced hands set the tone, showing the next wave of chemists and operators how to treat this molecule with respect—never fear, but always caution.
Future success with Crotonaldehyde will come from continued research and a willingness to invest in alternatives where possible. Researchers are now exploring catalysts that can steer Crotonaldehyde reactions toward desired products with less waste. Some teams are using enzyme-driven processes, taking cues from biological systems that handle aldehydes gently but efficiently. With the rise of green chemistry, more grants focus on creating pathways to bio-derived Crotonaldehyde, using agricultural byproducts like sugar beets or corn stover as starting material.
Adoption of these cleaner methods won’t be instant. Costs need to drop, and the chemistry must scale up in ways that meet the needs of both mega-factories and local workshops. Yet, incremental shifts happen all the time. Just last year, a plant in the Midwest began integrating a partially renewable Crotonaldehyde feedstock. While still supplementing with traditional sources, they showed that blending approaches can work. Sharing results through open-access journals and industry groups has amplified lessons, speeding up adoption elsewhere.
One promising avenue I've followed closely involves water-based applications. Traditional Crotonaldehyde mixes struggle with stability in water, spurring researchers to develop new derivatives that perform better in environmentally sensitive settings. This sort of upstream investment can make a tangible difference, especially for markets like agriculture, where run-off poses real risks. From my own work with cooperative farming groups, I’ve seen an eagerness to adopt safer formulations if the performance holds up. Bridging needs across fields—be it chemicals, agriculture, or waste reduction—keeps this molecule in the center of experimentation.
Statistics tell one story—volumes shipped, prices per ton, toxicity thresholds—but they don’t capture the full significance of Crotonaldehyde. It’s the combination of versatility, reactivity, and staying power that keeps it relevant as technologies evolve. Behind every figure are lives shaped by its presence, from plant engineers fine-tuning reactors in dense city districts to rural families keeping watch for chemical runoff. The decisions, both small and large, made about sourcing, handling, and disposing of this product matter in the long run.
My experience across different segments of the supply chain impresses one lesson above all: Crotonaldehyde’s impact is as much about human decision-making as it is about its molecular properties. The right choices—rigorous safety, smart innovation, honest communication—turn it from a risky raw material into a force that enables progress. As new challenges rise—climate, waste, health—the story of Crotonaldehyde will keep evolving, shaped by those willing to learn from the past and push into new territory.
Summing up Crotonaldehyde’s place in modern industry isn't about listing technical specs. It’s seen in the ways companies adapt processes to limit waste, the shift towards greener chemistry, and the thousands of skilled workers who manage risk every day. In a field often defined by sweeping regulations and shifting markets, Crotonaldehyde stands out for quietly enabling everything from flexible rubber products to new pharmaceutical compounds. Its differences from other aldehydes aren’t abstract: they're the reason it shows up in so many high-stakes, high-value contexts. As those demands grow more complex, Crotonaldehyde remains central, a testament to chemistry's potential when matched by people’s insight and care.