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HS Code |
974957 |
| Productname | 5-Amino-3-Bromobenzonitrile |
| Molecularformula | C7H5BrN2 |
| Molecularweight | 197.04 g/mol |
| Casnumber | 57964-57-7 |
| Appearance | Off-white to light brown solid |
| Meltingpoint | 108-112°C |
| Purity | Typically ≥98% |
| Solubility | Slightly soluble in water; soluble in organic solvents such as DMSO and DMF |
| Smiles | N#Cc1cc(N)cc(Br)c1 |
| Inchi | InChI=1S/C7H5BrN2/c8-6-2-5(4-9)1-7(10)3-6/h1-3H,10H2 |
| Storagetemperature | Store at 2-8°C |
| Synonyms | 3-Bromo-5-aminobenzonitrile |
As an accredited 5-Amino-3-Bromobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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| Shipping | |
| Storage |
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5-Amino-3-Bromobenzonitrile isn’t a household name, but in labs and research centers, it stands out for a good reason. A few years ago, when I first worked on aromatic nitrile compounds, I realized fast how essential molecular precision was for successful reactions. This compound, with its unique mix of an amino group, a bromine atom, and a nitrile moiety on a benzene ring, found uses that many beginners—myself included at the time—couldn’t predict until we saw the results for ourselves.
With its molecular formula of C7H5BrN2, 5-Amino-3-Bromobenzonitrile offers a unique chemical synergy. The amino group improves its reactivity, while the bromine atom adds versatility for further functionalization. In my early projects involving the synthesis of substituted benzenes, specificity mattered more than anything, and this compound’s structure fits right into the chemist’s toolkit. It brings a delicate balance: strong enough for robust reactions, yet selective enough to dodge troublesome side products, which always helped save time and resources in actual lab work.
A good chemical sees use beyond its basic structure, and here’s a story from my own experience. During a project on pharmaceutical intermediates, we needed a nitrile compound that could offer both an active functional group and a reactive halogen position. This compound’s amino group made it suitable for coupling reactions; at the same time, the bromine facilitated Suzuki or Buchwald-Hartwig cross-couplings. That allowed modifications at the core and the periphery, critical steps for synthetic chemists designing biologically active molecules.
Plenty of colleagues jumped on 5-Amino-3-Bromobenzonitrile for similar reasons—particularly the way the amino and bromo groups work together. When aiming to build up diverse benzonitrile derivatives, the combination brings far more options than simpler molecules like just bromo- or amino-benzonitrile. Each functional group opens a door: coupling, reduction, protection, or direct participation in multi-step pathways that lead to commercial products, especially active pharmaceutical ingredients and advanced agrochemicals.
Whenever we acquired 5-Amino-3-Bromobenzonitrile, purity and form always mattered. Most labs prefer materials with purity over 98% to avoid any headaches in downstream applications. In my lab days, even a one percent impurity sometimes meant having to troubleshoot for days. I learned to insist on powders or crystals that show consistent melting points—one trustworthy indicator of purity. If a batch showed a broad or inconsistent melting range, that often signaled problems that would get magnified in scale-up work.
Odor and color can help, too, in quick quality checks. Most of the time, the compound appears as an off-white to light beige crystalline powder. Any darkening or noticeable odors usually suggest decomposition—or contamination from the synthesis or storage process. A few years back, I saw a misguided batch that turned tan and had a stale scent. We traced it to poor storage in a humid corner of the warehouse, and that hard-won lesson stuck with me: quality starts before a single reaction runs.
Much of my appreciation for 5-Amino-3-Bromobenzonitrile came from its real-world adaptability. Medicinal chemists always hunt for scaffolds to build new drug leads, and this molecule steps up with its versatility. I knew fellow researchers who built entire compound libraries off its backbone while screening for kinase inhibitors. The nitrile group offers a handle for further derivatization, while the amino and bromo groups unlock a wide slate of modifications.
Beyond pharmaceuticals, specialty materials research taps into this compound, too. Electronic and optoelectronic sectors, especially organic semiconductors, need intermediates that play well in multi-step syntheses. 5-Amino-3-Bromobenzonitrile brings a balance of reactivity and stability, which suits those needs. The story repeats itself in agrochemicals, where efficient routes to active ingredients decide commercial success. Having a functionalized benzonitrile at hand allows researchers to speed up—or even skip—difficult steps and focus on testing the real-world properties of their candidates.
Some newcomers ask why not just use plain benzonitrile derivatives. My own work taught me that the fine details matter. 4-Bromobenzonitrile lacks the amino group, which limits its flexibility for nucleophilic substitutions or coupling chemistry. 5-Aminobenzonitrile, on the other hand, misses the bromo group, making it harder to extend the core or diversify substitution.
When both groups come together, the chemistry takes a leap. I remember conversations with synthetic chemists who highlighted that the combined features save weeks in multi-step syntheses. That practical impact can mean more than fancy reaction yields in an academic paper. Time spent troubleshooting or rerouting steps carries a real cost, whether measured in dollars or lost working hours. So, choosing 5-Amino-3-Bromobenzonitrile is less about theoretical appeal and more about making innovation sustainable in fast-paced industries.
Looking at catalogs over the years, it’s clear that not all 5-Amino-3-Bromobenzonitrile is created equal. Sources differ by purity, batch consistency, and storage history. Colleagues I trust always call vendors before placing large orders, asking about recent quality control data, shipping conditions, and even packaging methods. It’s not overkill; it’s a learned response from too many delayed projects caused by poor material quality. Sometimes, buying a slightly pricier grade pays off in reliability and confidence.
Moisture control ranks high, too, especially because the nitrile group doesn’t like water. Labs run into storage issues—lumps, hydrolysis, degraded product—if the material gets exposed. Good vendors know this and use desiccant packing or vacuum-sealed containers. I’ve seen resourceful teams go as far as splitting shipments into small daily-use portions, just to keep the rest in optimum condition. It’s all about keeping surprises to a minimum in the lab.
After participating in both academic and commercial R&D projects, I’ve come to believe that 5-Amino-3-Bromobenzonitrile acts like a backstage enabler in dozens of discoveries. In drug discovery, teams often begin with this building block to develop kinase and protease inhibitors, antibiotics, and inflammation modulators. By using this aromatic nitrile, chemists quickly create analogs and test structure-activity relationships—a process that can turn a promising scaffold into a marketable medicine. Global pharma pipelines—even those focusing on rare diseases—benefit from the molecule’s dual reactivity.
On the material science front, specialty polymers and dyes frequently originate from substituted benzonitriles. With the right tweaks, electronic properties improve, sometimes leading to new classes of sensors, emitters, or photovoltaic materials. During a collaboration last year, I saw an electronics team test a new compound library stemming from 5-Amino-3-Bromobenzonitrile, targeting improvements in charge-carrier mobility and operational stability in organic devices. While not every candidate moved to commercial trials, successes built on this molecule often pushed the envelope of what small aromatic compounds could do.
Agrichemical research also benefits. Synthesis teams constantly search for more effective crop protectants—efficient, easy to produce, and environmentally manageable. The ability to make rapid substitutions on the aromatic core while retaining key safety features helps keep innovation alive and field trials meaningful.
From a practical standpoint, batch scale-up and reproducibility stick out as recurring hurdles. In smaller synthesis runs, 5-Amino-3-Bromobenzonitrile behaves reliably, but certain transformations—like complex cross-couplings—demand careful attention to solvents, catalysts, and purification. I’ve solved unexpected drop-offs in yield by freshly distilling solvents or switching to higher-grade reagents after investigating trace impurities. It’s tedious work but pays off by reducing downstream failures.
Lab safety deserves a mention. Any chemical with a nitrile group requires thoughtful handling. I’ve seen labs implement extra ventilation and specialized glove use. Simple steps—promptly washing skin after accidental contact or ensuring good waste management—make a significant difference in long-term team health. Vendors who provide detailed, up-to-date safety guidelines (without burying them in unreadable documents) win trust and repeat business from research teams like the ones I’ve worked with.
Start with a sample batch. Before ordering a bulk quantity, it helps to validate both supplier and batch by running a pilot reaction. This practice saved me from wasted weeks more than once. If something feels off—a slightly different color, insoluble particles, an unusual smell—it’s better to spot it on a small scale. Sometimes, that’s the only way to maintain research quality and productivity.
Strong relationships with suppliers frequently pay dividends. Over the years, building real communication—asking specific questions, requesting COAs, sharing feedback—often meant suppliers gave an honest heads up about potential issues or let us know when a purer or freshly produced lot became available. That kind of back-and-forth doesn’t show up on spec sheets but makes a world of difference in smooth, long-term projects.
Demand for reliable, multifunctional building blocks keeps growing. Green chemistry is taking center stage, which means more attention for efficiency, waste reduction, and scalability. 5-Amino-3-Bromobenzonitrile fits these priorities due to its adaptability. By acting as a convergence point in synthetic pathways, it helps teams use fewer steps and less reagent, producing cleaner results and less waste. Scaling up from milligrams to kilograms feels less daunting when the starting material can pull double duty in key reactions.
Quality matters more than ever as regulations tighten and end-user expectations increase. Teams I know value traceable sourcing, lot-to-lot consistency, and the assurance that comes from real technical support behind every batch. Purity isn’t just a number; it translates into product quality, regulatory approval, and—most importantly—patient safety or environmental stewardship down the line.
Some say all aromatic nitriles end up acting the same, but experience shows otherwise. I’ve compared 5-Amino-3-Bromobenzonitrile to related materials in dozens of bench-scale syntheses. Having both a reactive amino group and a strategically placed bromo group opens up chemistries not feasible with mono-functional derivatives. The end result: greater synthetic flexibility and a higher chance of exploring uncharted chemical space. For my grad students, this molecular structure has often meant the difference between slow, single-purpose reactions and whole families of analogs appearing in just a few days.
Researchers working on limited budgets—common in academics—appreciate being able to stretch resources by using a single building block in different directions. Cutting the need for multiple starting materials improves logistics and reduces total spend. In commercial settings, the ability to rapidly pivot synthetic routes based on real-time screening feedback proves invaluable, especially in a world where speed-to-market makes or breaks projects.
From my own years at the bench, I can say that success stories build up through attention to detail. Choosing the right material, keeping it in prime condition, understanding subtle differences among similar compounds—all these small steps add up to progress. 5-Amino-3-Bromobenzonitrile won’t end up in news headlines, but in every team using it to create something new, its value comes through.
Besides its obvious roles in synthesis, it shapes the way research teams think about efficiency and adaptability. By opening the door to creative chemistry, it gives investigators room to chase big ideas while keeping projects grounded in practical, achievable goals. That’s something any lab can benefit from, no matter the final product.
I’ve learned most about 5-Amino-3-Bromobenzonitrile by following what works and asking hard questions after setbacks. In one project, yield drops led us to reassess every batch and reaction parameter. Only after discovering micro-impurities in a supposedly high-grade batch did we switch suppliers, which restored reaction efficiency and consistency. Every experienced chemist I know has a story like this, showing why product choice can’t be left to chance.
Another eye-opener came during a scale-up trial. Handling and weighing required dry-box procedures to avoid caking. Open air exposures changed melting points just enough to alter reaction kinetics. It’s easy to overlook tiny shifts at first, but those who pay attention to such details set themselves apart. Over time, these habits create a culture of rigor and reproducibility, cementing long-term trust with partners and end-users.
Transparent practices around sourcing, testing, and reporting purity help foster credibility. When research teams have direct access to recent analysis data, it saves time and boosts confidence in planning. In my circles, sharing honest feedback with suppliers—about positives and negatives—helped nudge them into tighter quality control. That cooperative loop keeps suppliers attentive and researchers assured that each shipment aligns with expectations.
Traceability now matters as much in specialty chemicals as it does in food or pharmaceuticals. Reliable product data, detailed batch histories, and open communication create a clearer path to meeting regulatory and market demands. That’s especially true as stakeholders—funders, partners, regulators—focus more on supply chain integrity across the scientific world.
5-Amino-3-Bromobenzonitrile stands out as more than an ingredient in a catalog—it’s a tool that allows researchers to stretch the boundaries of what’s possible in both established and emerging fields. Every project that passes through my hands leaves me more convinced that choosing and handling these core materials skillfully makes the real difference between average and exceptional outcomes.
While no single product solves every need, the value comes through in those labs and companies that see it as a foundation for creative problem-solving. For research, development, and innovation teams determined to run smarter and faster, this compound represents an investment in both flexibility and future discoveries. Even after years in the field, seeing what teams can accomplish with the right foundation brings satisfaction and a sense of progress that numbers alone never quite capture.