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HS Code |
561750 |
| Chemical Name | 2-Amino-5-Bromobenzonitrile |
| Cas Number | 3087-12-5 |
| Molecular Formula | C7H5BrN2 |
| Molecular Weight | 197.04 |
| Appearance | Light yellow to beige solid |
| Melting Point | 75-79°C |
| Solubility In Water | Slightly soluble |
| Purity | Typically >98% |
| Synonyms | 5-Bromo-2-cyananiline |
| Smiles | C1=CC(=C(C=C1Br)N)C#N |
| Inchi | InChI=1S/C7H5BrN2/c8-6-2-1-5(4-10)7(9)3-6/h1-3H,9H2 |
| Storage Temperature | Store at room temperature |
As an accredited 2-Amino-5-Bromobenzonitrile factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 2-Amino-5-Bromobenzonitrile is packaged in a 25-gram amber glass bottle with a secure, chemical-resistant screw cap. |
| Shipping | 2-Amino-5-Bromobenzonitrile is shipped in tightly sealed containers, protected from moisture and direct sunlight. It should be handled as a hazardous chemical according to local, state, and international regulations. Ensure appropriate labeling and documentation. Transport with care, using protective equipment and following all safety guidelines for toxic and potentially harmful substances. |
| Storage | 2-Amino-5-Bromobenzonitrile should be stored in a tightly closed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizers. Protect from moisture, light, and heat. Store under inert atmosphere if possible to prevent degradation. Properly label the container and keep it in a designated chemical storage cabinet, following all applicable safety and regulatory guidelines. |
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Purity 98%: 2-Amino-5-Bromobenzonitrile with purity 98% is used in pharmaceutical intermediate synthesis, where high selectivity and minimal byproduct formation are achieved. Melting Point 120°C: 2-Amino-5-Bromobenzonitrile with melting point 120°C is used in fine chemical manufacturing, where predictable thermal behavior supports process safety. Molecular Weight 197.03 g/mol: 2-Amino-5-Bromobenzonitrile with molecular weight 197.03 g/mol is used in agrochemical development, where accurate dosing yields consistent bioactivity. Stability Temperature 25°C: 2-Amino-5-Bromobenzonitrile stable at 25°C is used in chemical storage applications, where material integrity is maintained for extended periods. Particle Size <100 µm: 2-Amino-5-Bromobenzonitrile with particle size <100 µm is used in catalyst formulation processes, where increased surface area enhances reaction efficiency. Solubility in DMSO: 2-Amino-5-Bromobenzonitrile soluble in DMSO is used in biological assay preparation, where uniform dissolution improves experimental reproducibility. Moisture Content <0.5%: 2-Amino-5-Bromobenzonitrile with moisture content <0.5% is used in peptide synthesis, where low residual water minimizes unwanted hydrolysis. |
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Chemistry brings the world some remarkable raw materials, and few play as quiet but powerful a role as 2-Amino-5-Bromobenzonitrile. I know from spending time in both academic and industrial labs that you can always spot the really versatile compounds by how many different subjects are talking about them. This one keeps showing up, tucked into conversations about new pharmaceuticals or popping up in the plans for next-generation agrochemicals. You look at it on paper—a benzene ring with an amino group, a bromine at the five spot, a nitrile too. That small change can shift a whole reaction pathway, opening doors where other compounds hit dead ends.
The formula, C7H5BrN2, might seem unassuming, but there’s a lot of chemistry packed into those atoms. You find it as a white or pale yellow solid, and it melts at a fairly manageable temperature. In the lab, any chemist who’s spent time with aromatic chemistry knows nitriles stick around—they can survive a lot, but with the right tricks, you can coax them into something new. That’s the secret sauce here. The blend of an electron-withdrawing nitrile and a bromine atom with an electron-donating amino group makes this molecule a crossroads. You can see why so many synthetic routes lean on it as a key intermediate.
Let's talk about purity for a minute. Buying off-the-shelf 2-Amino-5-Bromobenzonitrile these days, of course, often means a product that’s at least above 97% pure—sometimes better, if you go for the top shelf. But the game is less about chasing every last trace of impurity and more about picking a grade that works for the job. I’ve seen researchers happy with “good enough” quality for early screening, then spring for ultra-pure batches for scale-up or final work. It makes sense. Trace metals or organic leftovers from the synthesis route don’t just harm yields—they can wreck complex multi-step routes that hinge on predictable reactivity.
The physical form matters too. A well-separated crystalline powder flows better and stores longer than lumpy, partially fused stuff. Storage isn’t just about shelf life; stable material makes every day easier. I’ve seen teams spend hours breaking up poorly handled powders, only to lose material in the process. Stable packaging, dry conditions, and real transparency about batch analysis save everyone a headache.
You’ll mostly hear about 2-Amino-5-Bromobenzonitrile showing up in the pharmaceutical world. Medicinal chemists love it because the combination of the amino, nitrile, and bromo substituents gives lots of room to customize. Nitriles are famous for helping molecules slip through cell membranes, and the aromatic ring keeps the base structure recognizable to natural systems, which often translates to bioactivity. Molecules derived from this compound end up in projects aimed at cancer, neurological disorders, and anti-infectives. Nobody talks about it as a final drug—rather, it’s a “skeleton key” that lets chemists test many different substitutions on the same backbone.
In agricultural chemistry, the same strengths translate directly. Researchers use it to build small molecules that interact with plant receptors or insect enzymes, aiming at better yield or more targeted pest control. It’s not about spraying 2-Amino-5-Bromobenzonitrile on fields—it’s about using its transformability to build something that works out in the field, holds up in the sun, but breaks down in the soil safely. Good chemical building blocks make it possible to iterate quickly through ideas in the lab, focusing on efficacy and environmental safety.
Laboratories focused on new materials take a similar tack. The bond formation options on this molecule enable connections to things like polymers and dyes. In specialty electronics or optical materials, creating exactly the right connections can mean the difference between success and failure on a product line. I’ve seen research papers that use 2-Amino-5-Bromobenzonitrile to anchor long organic chains, then add properties like electrical conductivity or color-shifting under light. For each field, the appeal isn’t about what this product does on its own, but how many doors it unlocks.
Big catalogs list hundreds of aromatic aminonitriles, and a quick scan makes it easy to think one’s as good as another. Not so. You might trade the bromine for a chlorine or another halogen. That small difference on the ring means a lot to the team working on a new inhibitor for an enzyme or a ligand for a metal complex. Bromine sits in the sweet spot for certain key reactions—big enough to guide selectivity, but less likely to throw off the molecule’s overall behavior compared to something much bulkier.
Switching the position of the bromine, even by a single spot, creates subtle shifts in reactivity. The five-position on the ring puts the bromine just far enough from the amino group that both can participate in different kinds of reactions, giving more options in cross-coupling, nucleophilic substitution, and cyclization cascades. Some will argue for using the 4- or 6- isomer if those fit a targeted scaffold, but for breadth and reliability, the 5-bromo flavor is a frequent favorite.
Purity makes a difference too, especially compared to related compounds that sometimes arrive with higher moisture or trace side products. I saw one project where a cheaper lot seemed “fine” on the specs, but ran into trouble during Suzuki coupling—the trace impurities from incomplete bromination led to extra by-products. That meant more chromatography, more waste, and an annoyed project manager. Having reliable analytical backing on every order prevents these headaches.
No honest commentary skips over safety. Handling aromatic aminonitriles brings some basic but strict rules. Gloves, eye protection, good ventilation. Industrial users often automate or enclose their workflows, minimizing risk of exposure. Many nitriles can irritate lungs or skin with too much contact, and the aromatic structure means it shouldn’t go down the sink or out the window. Waste disposal, both for unused product and by-products, needs real attention, not just “toss it in the bin.” In every serious lab, the colleagues who keep to their safety routines are the ones who stay healthy long-term.
Transportation and storage tighten up these routines. It makes sense—while the raw material itself isn’t especially volatile or flammable, keeping it dry and cool keeps reactions predictable and finished product safe. I always check for up-to-date safety data from suppliers, since the best companies keep this information front and center. It’s not only about compliance; mistakes in chemical handling can set back research and harm people.
There’s something to be said for picking a supplier that stands by the material long after the invoice. In labs where new chemists show up each year, consistent product and clear documentation make mentoring simpler. I’ve watched smart students waste days trying to figure out why yields dropped, only to learn their lot of raw material didn’t match the old batch in granularity or purity. Companies making 2-Amino-5-Bromobenzonitrile with tight lot-to-lot reproducibility solve these problems at the source.
Ethical sourcing means a lot, too. It’s tempting to order from wherever’s cheapest. But as regulations get stricter and traceability matters to customers, the origin of your chemical inputs becomes as important as their spec sheet. Avoiding child labor, paying attention to environmental impact, and respecting local laws isn’t just about avoiding bad headlines—it’s about being part of a supply chain people can trust. I’ve seen projects fall apart because partners couldn’t provide basic documentation; investing in responsible suppliers keeps everyone out of hot water.
Green chemistry is another area where real progress is possible. The synthesis of 2-Amino-5-Bromobenzonitrile typically follows either a direct bromination of aminobenzonitrile or a nucleophilic aromatic substitution. Each route generates waste and uses hazardous reagents. The push to streamline these steps by employing more selective catalysts, recycling solvents, and cutting out harsh reagents isn’t just a feel-good trend. It shaves dollars off production costs and makes downstream regulatory approval smoother for pharmaceutical applications. Teams working with newer methodologies, like continuous flow chemistry or greener oxidants, set the stage for safer labs and lower emissions.
What does it take to make the chemical industry both productive and sustainable? I’ve participated in enough workshops and trade fairs to see the central role of proactive investment—whether in equipment, training, or supplier partnerships. 2-Amino-5-Bromobenzonitrile serves as a good example of how these investments pay off in speed, safety, and market responsiveness.
So, what works? Regular training on safe use for everyone, from new lab techs to Principal Investigators. A culture where people stop and report strange odors, leaks, or suspicious containers without the fear of blame. Open conversations with suppliers when quality slips, and keeping real records about product performance tied to the exact batch. Transparent specification sheets, routine batch testing, and open communication between buyer and seller keep small issues from killing timelines.
Labs interested in sustainability start with simple steps, like recovering unused 2-Amino-5-Bromobenzonitrile after a batch process and ensuring old bottles get disposed through the right channels. More advanced outfits work with suppliers to develop greener synthetic routes, sharing the benefits as well as the risk. If a single batch cuts both cost and environmental impact, everyone wins. Collaboration—across companies, between academia and manufacturers, and between buyers and sellers—drives improvement faster than waiting for regulations to force compliance.
Technology helps too. Analytical equipment has come down in price, and even smaller labs now routinely check for trace impurities themselves by NMR or HPLC. This democratization of testing means mistakes get caught early, consistency improves, and feedback loops speed up. With solid data in hand, chemists can push for refinements in the supply chain—better purifications, improved packaging, or tweaks to synthesis that double yields and halve waste.
The online chemical marketplace has made variety and sourcing incredibly fast, but it’s easy to lose sight of the people and practices behind every shipment. Experience teaches us that strong professional relationships yield the best results. Trust matters. When teams know their inputs will arrive on time, match specifications, and come with all documentation, they focus on what matters—making the next new molecule, finishing a project, or teaching new researchers the ropes without unnecessary stress.
If you walk into any chemistry lab today, you’ll find more people focused on applications and impact than ever before. The building blocks they use have to keep pace—not just in reactivity, but in quality, sustainability, and safety. 2-Amino-5-Bromobenzonitrile fits into this new world because it sits at the intersection of tradition and innovation. Its structure and reactivity have powered thousands of research papers and patent filings, while new standards in sourcing and synthesis point toward a more responsible industry.
Chemists and managers alike balance the drive to move fast and get results with the responsibility to do the job safely and ethically. Working with reliable chemical building blocks makes that balancing act a little simpler. Teams coordinate across continents or across a hallway; buyers look for both flexibility and accountability; scientists demand consistency and transparency.
Every purchase and every experiment says something about where the industry’s going. Whether that’s pursuing new medicines, safer food production, or better functional materials, the choices made in the supply chain echo throughout the broader chemical ecosystem. Getting the fundamentals right in products such as 2-Amino-5-Bromobenzonitrile—the quality, documentation, ethical production, and support behind each shipment—builds a strong foundation for discovery and for trust with colleagues and customers.
Some parts of chemistry don’t get flashy headlines. The world runs quieter but deeper for compounds like 2-Amino-5-Bromobenzonitrile, which slip into a hundred exciting projects and emerge transformed into something brand new. Chemists trust these building blocks because they’ve seen what reliable, responsible suppliers can help them achieve. As regulations shift, as customers expect more transparency, and as scientific frontiers move fast, the importance of core ingredients only grows.
Those who work in the field recognize that excellence rarely comes from a single breakthrough. It’s the daily attention to detail, the willingness to test and adapt, and the choice to work with suppliers who align with both technical needs and ethical priorities. With the right partners and proven raw materials, limits fade and possibilities expand. For labs that want to make a difference—whether in healthcare, agriculture, or new technologies—the right foundation starts with the basic chemicals they trust. Out of all the options on the shelf, 2-Amino-5-Bromobenzonitrile stands out not for its flash, but for the quiet, powerful role it plays in moving science forward.