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HS Code |
212476 |
| Chemical Name | 5-Bromopyridine-2,3-diamine |
| Molecular Formula | C5H6BrN3 |
| Molecular Weight | 188.03 g/mol |
| Cas Number | 5423-14-3 |
| Appearance | Light brown to brown solid |
| Melting Point | 160-164°C |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO, slightly soluble in water |
| Smiles | C1=CC(=NC(=C1N)N)Br |
| Inchi | InChI=1S/C5H6BrN3/c6-3-1-2-4(7)9-5(3)8/h1-2H,7-8H2 |
| Synonyms | 2,3-Diamino-5-bromopyridine |
| Storage Conditions | Store at 2-8°C, in a tightly sealed container |
As an accredited 5-Bromopyridine-2,3-diamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 10-gram amber glass bottle with a tightly sealed screw cap, labeled `5-Bromopyridine-2,3-diamine`, and hazard information displayed. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 5-Bromopyridine-2,3-diamine involves securely packing drums or bags, ensuring safe transport and compliance. |
| Shipping | **Shipping Description for 5-Bromopyridine-2,3-diamine:** Ships in tightly sealed containers, protected from moisture and light. Handled as a hazardous chemical—may require labeling as harmful or irritant. Transport complies with relevant chemical safety regulations. Store at room temperature. Ensure documentation for chemical identification accompanies shipment. Use protective packaging to prevent leaks or contamination during transit. |
| Storage | 5-Bromopyridine-2,3-diamine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from incompatible substances such as strong oxidizing agents. Keep the container protected from light and moisture. Store at room temperature, and ensure that proper labeling and chemical safety protocols are followed to prevent accidental exposure or contamination. |
| Shelf Life | 5-Bromopyridine-2,3-diamine should be stored in a cool, dry place; shelf life is typically 2-3 years if unopened. |
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Purity 98%: 5-Bromopyridine-2,3-diamine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and minimal byproduct formation. Melting point 148°C: 5-Bromopyridine-2,3-diamine with a melting point of 148°C is used in high-temperature organic reactions, where it provides consistent thermal stability. Molecular weight 188.01 g/mol: 5-Bromopyridine-2,3-diamine of molecular weight 188.01 g/mol is used in medicinal chemistry research, where accurate mass supports precise compound formulation. Particle size ≤50 µm: 5-Bromopyridine-2,3-diamine with particle size ≤50 µm is used in fine chemical manufacturing, where small particles enhance solubility and reaction efficiency. Solubility in DMSO: 5-Bromopyridine-2,3-diamine soluble in DMSO is used in drug screening assays, where it improves compound delivery in biological systems. Stability temperature up to 80°C: 5-Bromopyridine-2,3-diamine with stability up to 80°C is used in polymer modification processes, where maintained integrity allows for extended processing times. Low moisture content ≤0.5%: 5-Bromopyridine-2,3-diamine with moisture content ≤0.5% is used in catalyst preparation, where low water content prevents catalyst deactivation. |
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In today’s research-driven world of chemical manufacturing, access to versatile compounds can shape a project’s direction and even its success. Among these multifaceted molecules, 5-Bromopyridine-2,3-diamine stands out for its structure and range of application. Many chemists and product developers have called on it for critical steps in drug research, agrochemical discovery, and advanced materials science. Having tested and worked with related pyridine derivatives, I’ve seen the value these intermediates bring to synthetic pathways—not just for what they enable, but for the efficiency and reliability they offer. Companies and research teams that rely on precision reach for building blocks that won’t lock them in or set off unwanted side reactions, and this is where 5-Bromopyridine-2,3-diamine has earned its place.
The molecule’s structure—a pyridine ring carrying both amino groups and a strategically placed bromine atom—means it serves as more than just another aromatic amine. Each substitution gives chemists a handle for further reactions. From my time in the lab, direct substitutions and coupling reactions often benefit from the reactivity of bromo groups. The 5-bromo position resists unwanted migration, making selectivity more manageable and final product yields more reliable. The diamine features, located at the 2 and 3 positions, provide multiple sites for functional group modification, which comes in handy when exploring libraries of related compounds, such as those in pharmaceutical lead optimization or advanced pigment development.
Purity drives many of the choices people make when sourcing intermediate chemicals like this. From first-hand experience, high-purity compounds lower the risk of side reactions and reduce troubleshooting time down the line. Most laboratories working on sensitive applications, especially those touching regulated industries like pharmaceuticals, demand better than 98% purity levels—not because it’s a marketing claim, but because every extra contaminant costs precious time in column chromatography, failed reactions, or questionable analytical results. 5-Bromopyridine-2,3-diamine is available with these high standards. Lot traceability, consistent melting point, and HPLC or NMR characterization mean fewer unpleasant surprises and greater confidence each time a new shipment arrives. This reliability isn’t just about peace of mind; it reflects a commitment to reproducibility in research and manufacturing. Without it, projects stall or derail, budgets tighten, and credibility takes a hit.
One major draw of this compound comes from its role as a launch point for a wide range of downstream syntheses. Over the years, I’ve seen colleagues use it for constructing complex heterocyclic scaffolds, particularly in medicinal chemistry programs. The pharmaceutical field often uses halogenated pyridines like 5-Bromopyridine-2,3-diamine for bioisosteric replacements or as frameworks for kinase inhibitors, antibiotics, and central nervous system agents. Rational drug design often calls for rapid iteration of small molecule libraries; using robust, well-characterized building blocks speeds up the process and helps maintain consistency from batch to batch.
In agriculture, pyridine derivatives appear in investigations for new herbicides, fungicides, and insecticides. Reliable access to molecules like 5-Bromopyridine-2,3-diamine allows research teams to explore new biological targets. As environmental regulations tighten and resistance patterns change, the pressure grows to deliver safer, more selective agents. Each new idea starts with the right chemical tools, and the unique substitution pattern here lends itself to creative modifications—such as coupling with carbamates, ureas, or sulfonamides.
People often wonder what sets this compound apart from other halogenated pyridines or aromatic diamines. Comparing its structure to something like 2,3-diaminopyridine without the bromine shows a clear difference in reactivity. The bromine changes both the electron density and the physical properties of the molecule—sometimes altering solubility, most noticeably influencing reaction speed in Suzuki or Buchwald-Hartwig couplings. From what I’ve seen in real project work, having the bromo substituent at the 5-position alters the preferred site for further substitution, presenting opportunities for chemoselective modifications that wouldn’t be possible with unsubstituted analogs.
Other halogenated pyridines exist, but each position and each halogen brings a different set of trade-offs. Chlorinated analogs sometimes lack the leaving group ability needed for smooth coupling reactions; iodine’s lower availability and higher cost can make scaling impractical. Fluorinated systems behave differently due to the position’s electron-withdrawing strength, causing downstream reactivity to change. 5-Bromopyridine-2,3-diamine strikes a balance—offering both synthetic accessibility and reliable reactivity.
From a hands-on perspective, 5-Bromopyridine-2,3-diamine is stable under regular laboratory conditions. It usually takes the form of a light solid, with modest sensitivity to moisture. Good storage practices—keeping the container closed in a cool, dry place—prevent unnecessary clumping or decomposition. Comparing this to other sensitive intermediates, it’s forgiving; it does not fume or corrode most standard packaging. Routine handling still requires personal protective equipment, ventilation, and avoidance of contact, particularly because aromatic amines sometimes pose a risk for skin sensitization. Good lab habits matter, as anyone who has dealt with cross-contamination or sample degradation can attest.
Sustainability in fine chemicals means more than just following regulations. Synthetic chemists prefer straightforward, atom-efficient routes with minimal waste. Several commercial processes for producing 5-Bromopyridine-2,3-diamine start from easily sourced precursors, relying on bromination and amination steps that avoid harsh conditions or excess byproducts. My experience in process development shows that clean, high-yielding steps reduce costs and environmental impact. As green chemistry standards grow more important, manufacturers keep refining these methods—sometimes partnering with universities to develop catalytic techniques that cut down on toxic reagents and harsh solvents.
Scalability also plays a significant role. Research work often begins with gram or multi-gram quantities, but pilot and production batches demand kilogram or even ton-scale synthesis. It is reassuring to observe that 5-Bromopyridine-2,3-diamine has made this leap: its synthesis does not require exotic reagents or rare metals, removing major supply chain obstacles. Companies looking to forecast their growth or meet new regulatory standards value this kind of predictable supply. Over the last decade, the specialty chemicals market’s growth has meant more reliable access and more competitive pricing.
Chemical purity and lot consistency drive trust among users. Analytical methods such as NMR spectroscopy, mass spectrometry, and high-performance liquid chromatography verify both identity and purity for every batch. These practices reflect not only good manufacturing standards but a dedication to science and customer needs. I have worked with suppliers who issue certificates of analysis, and the difference is clear: clear documentation speeds up regulatory filing and lowers the cost of unexpected disruptions. For companies preparing to submit new pharmaceutical candidates or crop protection agents, any deviation in quality demands costly investigation and sometimes repeats of key, time-consuming experiments.
Traceability back to raw materials and process steps provides peace of mind. As supply chains stretch across regions, customers care about ethical sourcing and environmental impact. If a company cannot trace its inventory and account for its raw materials, it risks losing business in regulated markets. This demand for documentation applies not just to big players: small-volume custom synthesis houses face the same requirements when serving biotech startups or public sector labs.
The field’s pace only accelerates. Custom molecules drive discovery, but without reliable intermediates like 5-Bromopyridine-2,3-diamine, innovation slows. In my years of work, I’ve seen promising projects fail for lack of an available or affordable intermediate, or technical teams forced to abandon certain synthetic plans when the building blocks just did not exist at scale or couldn’t be purified to needed specifications.
Experience teaches that availability and support matter nearly as much as a material’s properties. Technical teams benefit from responsive suppliers who provide up-to-date safety information, storage guidelines, and answers for technical troubleshooting. This also extends to questions on downstream use: for example, whether a bromoamine will withstand certain metal-catalyzed couplings, or remain stable through multiple purification steps. Companies who keep the user’s real needs in mind—backed by robust science and customer insight—win long-term confidence.
R&D work never stays still for long. The field of functional materials, particularly for electronics and sensing applications, has started turning to brominated pyridine derivatives for tuning electronic properties and solubility. 5-Bromopyridine-2,3-diamine, with its ready modification points, lets teams try out new ligands and supports for organometallic frameworks. The overlap with life sciences grows, as small molecules inspired by natural or bioactive templates move from lab to clinical trials.
Patents and scientific papers often cite this molecule in new synthesis routes. Researchers who need to access rare or complex heterocycles commonly retrofit existing routes with intermediates like this. The public scientific record supports its value: journals across organic, medicinal, and materials chemistry describe its uses, both as an end product and as a flexible scaffold. What was once considered specialty or niche now stands as a reliable workhorse for many different industries.
No critical intermediate comes without its challenges. One recurring issue is limited data on long-term environmental fate, especially as regulations keep evolving. Similar aromatic amines have raised concerns for aquatic toxicity or persistence in some jurisdictions. Addressing this, companies and researchers can expand studies on degradation pathways and seek greener alternatives for waste disposal. Experience reminds us that designing out hazards early pays dividends in sustainable business and regulatory compliance. If more chemists use analytical monitoring for residues and develop less hazardous synthetic routes, the whole industry benefits.
There’s also the question of cost and access for early-stage researchers and small enterprises. Chemical intermediates with robust demand often drive competition, but spikes in raw material cost or transport disruptions create headaches. More transparent supply chains, vertical integration, or cooperative purchasing groups can help level access. Suppliers investing in local inventory or improved logistics will see stronger partnerships with the R&D world.
Beyond product launches, the presence of well-characterized building blocks changes the landscape for researchers and students. Laboratories teaching synthetic methods benefit from using real-world, relevant compounds in their protocols. I have seen new scientists gain confidence and skill by running successful reactions with reliable starting materials. This affects morale, learning, and willingness to tackle more complex chemistry.
Small and medium-sized companies, including those in emerging markets, also gain access to the innovation ecosystem by obtaining the same high-quality intermediates as their multinational competitors. By leveling the quality playing field, innovation becomes more about the best idea and less about privileged access.
5-Bromopyridine-2,3-diamine sets a high bar as a chemical intermediate that not only meets technical requirements but actually helps shape research and product development outcomes. Through dependable supply, proven quality, and adaptability to demanding contexts, it supports advances across pharmaceuticals, agriculture, materials science, and education. Its select combination of bromine and amine groups brings versatility without sacrificing reliability. The stakes keep growing as customers demand both performance and responsibility.
The future belongs to those who choose and manage their building blocks wisely. Transparency, real customer support, environmental responsibility, and a respect for science can all be found in each vial or drum of 5-Bromopyridine-2,3-diamine—provided the industry’s best practices hold firm. The pathway from the benchtop to the marketplace runs smoother when robust intermediates are available, helping scientists focus on discovery, not on avoidable problems. With compounds like this, ambitious ideas get a fighting chance, and the next big breakthrough comes within reach.