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HS Code |
901454 |
| Productname | 4-Bromoacetylbenzonitrile |
| Casnumber | 39085-42-8 |
| Molecularformula | C9H6BrNO |
| Molecularweight | 224.06 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 133-136 °C |
| Boilingpoint | No data available (decomposes) |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Refractiveindex | No data available |
| Density | No data available |
| Smiles | CC(=O)C1=CC=C(C#N)C=C1Br |
| Inchikey | XVUSHZKMBZKHKW-UHFFFAOYSA-N |
As an accredited 4-Bromoacetylbenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 25-gram amber glass bottle labeled "4-Bromoacetylbenzonitrile," sealed with a screw cap, includes hazard symbols and product details. |
| Shipping | 4-Bromoacetylbenzonitrile is shipped in tightly sealed containers, protected from moisture and light, under ambient temperature conditions. Proper labeling and documentation are included, with all handling and transportation complying with chemical safety regulations. The package should be handled by trained personnel, ensuring safe delivery to laboratories or facilities. |
| Storage | 4-Bromoacetylbenzonitrile should be stored in a tightly sealed container, away from moisture, heat, and direct sunlight. Keep it in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure the storage area is clearly labeled and access is limited to trained personnel. Follow all relevant safety guidelines and regulations. |
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Purity 98%: 4-Bromoacetylbenzonitrile with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield product formation. Melting Point 90–94°C: 4-Bromoacetylbenzonitrile with melting point 90–94°C is used in organic reaction optimization, where it enables reliable crystallization and isolation. Stability Temperature 25°C: 4-Bromoacetylbenzonitrile with stability temperature 25°C is used in ambient storage of chemical libraries, where it maintains compound integrity over time. Particle Size <100 μm: 4-Bromoacetylbenzonitrile with particle size less than 100 μm is used in solid-phase synthesis protocols, where it provides uniform dispersion and reactivity. Molecular Weight 224.04 g/mol: 4-Bromoacetylbenzonitrile with molecular weight 224.04 g/mol is used in fine chemical manufacturing, where it contributes to precise formulation and dosage control. HPLC Purity >98%: 4-Bromoacetylbenzonitrile with HPLC purity greater than 98% is used in analytical reference standards, where it guarantees accurate quantification and validation. Low Moisture Content: 4-Bromoacetylbenzonitrile with low moisture content is used in moisture-sensitive reactions, where it prevents hydrolysis and preserves product quality. Assay 99%: 4-Bromoacetylbenzonitrile with assay 99% is used in custom synthesis of agrochemical intermediates, where it maximizes reaction efficiency and minimizes impurities. |
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In the fast-paced world of chemical research and manufacturing, the search for stable and reliable building blocks feels never-ending. 4-Bromoacetylbenzonitrile stands out thanks to its practical advantages and track record in organic synthesis. This compound, long trusted by bench chemists and commercial producers alike, serves as a backbone for a surprising variety of projects, especially where precision and reproducibility are critical. The molecular formula—C9H6BrNO—gives a hint of the complexity waiting beneath the surface. Its solid form and reliable purity levels mean less second-guessing during downstream reactions, saving time and reducing surprises.
The experience of handling 4-Bromoacetylbenzonitrile starts with its unmistakable white-to-off-white crystalline appearance. Sharp melting points often fall between 97°C and 101°C, signaling strong batch consistency. Reporting purity above 98% has become standard for most modern suppliers, though labs demanding the highest confidence often wave a GC or HPLC certificate over every new bottle. It’s not just about numbers—what matters is watching reactions tick along as scheduled, without unexplained hiccups. Every step, from measuring to dissolving, proceeds predictably. Years on the bench have taught me to appreciate that steadiness; it beats wrestling with mystery side products every time.
The main reason researchers and manufacturers turn to this compound involves its dual functional groups. Placing a bromine atom on a benzene ring, then adding both a nitrile and an acetyl group, creates a highly reactive intermediate ready to dive into all sorts of transformations. Academic teams find it indispensable when exploring new heterocycles, pushing boundaries in medicinal chemistry, or seeking to customize ligands for analytical work. Pharmaceutical companies value it for its versatility in key steps, where trace contamination can break an entire synthesis chain. From simple alkylations to the creation of more elaborate aromatic systems, it gives chemists control over both reactivity and selectivity—two prized traits during any scale-up process.
Every project leader gets bombarded with choices: Which building block delivers the reliable results we need, without overpaying or complicating the waste stream? Here’s where my direct experience with 4-Bromoacetylbenzonitrile makes the difference. Some labs reach for bromobenzene, but the single functionality limits what you can do in fewer steps. Others try more exotic nitrile- or acetyl- substituted benzenes, hoping for cost savings or faster reactivity. I’ve seen headache after headache—impurities that can’t be tracked, intermediates that refuse to crystallize, and purification nightmares. 4-Bromoacetylbenzonitrile avoids these common pitfalls.
The positioning of the bromine atom on the 4th carbon makes this compound unique. Many alternative molecules stick halogens on other positions. That subtle shift seems minor until a reaction stalls or generates regioisomers that eat up more time in the lab. The structure of 4-Bromoacetylbenzonitrile delivers the kind of predictability that’s hard to find elsewhere. If the project hinges on quick and reliable nucleophilic substitutions or Suzuki couplings, repeats across batches are more likely with this option.
People might think products like this belong mostly in academic labs, but that’s not what I’ve seen. Commercial labs use it when ramping up new pesticides and agrochemical intermediates. Specialty polymer teams rely on the reactivity of its acetyl group for custom cross-linking. Even electronics manufacturers need this exact structure to test new resins meant for precision parts. In all these settings, the shared goal stays the same: build something clean, reproducible, and reliable enough to scale beyond a round-bottom flask.
Showing up in research papers is one metric, but I judge a chemical’s importance by how much time it saves out in the real world. In several projects, using 4-Bromoacetylbenzonitrile meant skipping extra column purification steps or avoiding repeated failures in key couplings. The cost savings over six months add up, not to mention the reduced solvent use. No one wants to repeat the same pilot batch three times because of mystery contaminants—a lesson learned the hard way by research teams across the globe. The compound’s clean reactivity leads to fewer unknowns, making the next step in the process far less stressful.
Any experienced chemist will tell you that the price tag on a reagent is only part of the story. There’s always the risk of inconsistent batch-to-batch quality when searching for cheaper alternatives. With 4-Bromoacetylbenzonitrile, the typical supplier offers full specs up front, and you can actually trust what’s on the label—rare in a market crowded by third-party resellers and obscure sources. Poor-quality reactants lead to wasted time and sometimes months of troubleshooting. I’ve watched labs try to shave costs, only to spend ten times as much fixing their synthetic protocols later on. In a landscape where projects ride on thin margins and tough deadlines, using a product with dependable consistency makes sense every time.
Nobody likes to talk about the dangers in chemistry, but honesty builds better habits. 4-Bromoacetylbenzonitrile requires respect. It’s a strong irritant, and like most reagents containing bromine and nitrile groups, it deserves careful handling. I always reach for good quality gloves and make sure to open containers inside the fume hood. Spills clean up easily without nasty odors, which is a relief compared to nastier relatives. Keeping it dry and capped ensures stability over many months. Whether you work in a lean startup or a sprawling institutional lab, maintaining basic safety discipline around this compound pays off down the road.
Some chemists I know worry about storage issues with trickier halogenated intermediates. 4-Bromoacetylbenzonitrile, in my experience, holds up in ambient conditions—as long as you keep it away from moisture and light. Decomposition isn’t common unless you push the limits, another point in its favor compared to less robust analogues. For bulk users running non-stop syntheses, confidence in storage and shipping saves on time and paperwork. It’s not just about safety for its own sake, but about reducing risk in the bigger picture.
Production trends in the specialty chemicals sector show that demand continues shifting toward reagents that can streamline both workflow and waste management. 4-Bromoacetylbenzonitrile, thanks to its efficiency, lets companies tighten up their synthetic steps, minimize by-products, and often recover more material from each run. Environmental concerns might not drive every research budget, but improved yields and fewer repeated syntheses cut down the use of solvents and energy—a direct savings to the bottom line and the community at large.
Downsides arise if sourcing veers toward poorly regulated suppliers, where environmental compliance falls through the cracks. Responsible sourcing builds in sustainability from the start. I’ve seen companies audit their supply chains closely, and products like 4-Bromoacetylbenzonitrile become a go-to partly because they’re easier to track. Improved traceability makes regulatory reporting easier and lets buyers support factories that avoid corner-cutting practices. Pressure from customers and regulators for greater transparency only amplifies this shift.
Trying new chemical routes always comes with some risk. Any time I worked through a multi-step synthesis, I wanted intermediates that wouldn’t throw curveballs. In one notable case, needing a reliable aryl bromide pushed me toward 4-Bromoacetylbenzonitrile after two other candidates gave mediocre yields or required expensive purification columns. The switch paid off—my product crystallized in good shape, and the follow-up steps fell into place, saving over a week of work and a lot of stress. Notes from colleagues back up this finding. Teams building small-molecule libraries prefer this compound for the same reasons: flexibility, consistency, and purity. It works as both nucleophile and electrophile in various scenarios, letting you branch out in synthetic planning instead of backing yourself into a corner.
In medicinal chemistry, every failing synthesis delays actual testing and slows down the drug discovery pipeline. Pressure to keep novel candidate compounds flowing keeps teams looking for trusted reagents with broad applicability. 4-Bromoacetylbenzonitrile’s popularity among grad students and contract manufacturers reflects its practicality and reliability. Experienced researchers know they cut more corners in downstream steps if their core intermediates start with high purity. There’s nothing glamorous about choosing the right building block, but projects live or die on choices like these.
Sometimes, the field gets swept up in excitement about new coupling techniques or designer reagents. While innovation keeps chemistry moving forward, it also pays to recognize what already works. 4-Bromoacetylbenzonitrile earns loyalty not through flash, but through solid performance across diverse reaction types. For those teaching undergraduates, demonstrating successful runs and troubleshooting with a forgiving, well-known compound helps students grasp core principles. For industrial chemists, it’s about hitting production targets reliably, supporting both pilot and commercial scale syntheses without adding uncertainty at any stage.
Competition between suppliers can tempt buyers to experiment with alternatives, but reliability often wins out. The incentive to switch shrinks once you’ve seen the savings from avoiding wasted runs. Over the years, I’ve watched seasoned researchers return to this compound over and over—not out of habit, but because scaling up with a trusted intermediate means fewer sleepless nights. In labs where turnover is high and time to train newcomers is short, sticking with consistent, familiar products gets results everyone can count on.
Looking at the big picture, the appeal of 4-Bromoacetylbenzonitrile doesn’t stem from marketing gloss or vague buzzwords. Its record of solid results across academic, pharma, and specialty chemical arenas anchors its growing importance. Down the supply chain, distributors know it means fewer complaints and returns. For project leads managing large teams or multinational operations, the product’s history of quality gives them confidence to focus on innovation and efficiency elsewhere.
It’s easy to overlook such a plain-looking compound for flashier molecules, but anyone responsible for milestones understands the high stakes. With every task—whether a routine substitution or a new route to a functionalized benzonitrile—the right building block preserves resource agility and lets creative thinking shape the rest of the process. In my own experience, teams who standardize around proven reagents like this one save not only on materials, but on time lost navigating unexpected setbacks. Relationships between teams, managers, and external partners also benefit when the basic chemistry just works as intended.
The market keeps shifting, as new molecules join the shelves and synthetic needs continue to evolve. Yet the core values for chemical sourcing—and success—focus on trust, efficiency, and safety. 4-Bromoacetylbenzonitrile supports these priorities by balancing versatility and quality control. Lessons learned from countless synthesis runs, collaborative projects, and hours spent fixing others’ mistakes all point to the same conclusion: some building blocks outperform their competition in ways that truly matter day to day.
For researchers just starting their journey, settling on a tested intermediate simplifies both planning and execution. For experienced chemists, the reduced risk and improved reproducibility align perfectly with the growing expectation for reliable, efficient, and safe practices. In an industry defined by progress, solutions that quietly deliver without fanfare will always have a place at the bench. 4-Bromoacetylbenzonitrile proves that well-designed, well-made compounds still form the backbone of real-world innovation—one clean reaction at a time.