|
HS Code |
148617 |
| Chemical Name | 5-bromo-N4-ethylpyridine-3,4-diamine |
| Molecular Formula | C7H10BrN3 |
| Molecular Weight | 216.08 g/mol |
| Cas Number | 1211510-33-8 |
| Appearance | Solid |
| Purity | Typically >98% (as sold commercially) |
| Storage Conditions | Store at room temperature, in a dry and well-ventilated place |
| Synonyms | 5-Bromo-3,4-diamino-N-ethylpyridine |
| Smiles | CCNC1=NC=C(C(=C1)N)Br |
| Inchi | InChI=1S/C7H10BrN3/c1-2-10-7-5(8)6(9)3-4-11-7/h3-4H,2,9H2,1H3,(H,10,11) |
| Application | Research chemical/intermediate |
As an accredited 5-bromo-N4-ethylpyridine-3,4-diamine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | A 1-gram amber glass vial with a screw cap, labeled "5-bromo-N4-ethylpyridine-3,4-diamine," with safety and hazard information. |
| Container Loading (20′ FCL) | 20′ FCL container: Packs 5-bromo-N4-ethylpyridine-3,4-diamine in HDPE drums, net weight approximately 8-10 metric tons per container. |
| Shipping | **Shipping Description:** 5-Bromo-N4-ethylpyridine-3,4-diamine should be shipped in tightly sealed containers under ambient or recommended temperature conditions. The package must be clearly labeled, compliant with relevant hazardous material (HazMat) regulations. Use protective secondary packaging to prevent breakage or leakage. Ship with appropriate documentation, including safety data sheets (SDS), via approved carriers. |
| Storage | Store **5-bromo-N4-ethylpyridine-3,4-diamine** in a tightly sealed container in a cool, dry, and well-ventilated area. Protect from light, moisture, and incompatible substances such as strong oxidizers. Clearly label the container and keep it away from food and drink. Access should be restricted to trained personnel, and appropriate personal protective equipment should be used when handling the chemical. |
| Shelf Life | Shelf life of 5-bromo-N4-ethylpyridine-3,4-diamine: Stable for 2 years if stored sealed, dry, and protected from light at 2-8°C. |
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Purity 98%: 5-bromo-N4-ethylpyridine-3,4-diamine with 98% purity is used in pharmaceutical intermediate synthesis, where it enables high-yield and low-impurity product formation. Melting Point 120°C: 5-bromo-N4-ethylpyridine-3,4-diamine with a melting point of 120°C is used in solid-state formulation development, where it ensures thermal stability during processing. Solubility in DMSO 50 mg/mL: 5-bromo-N4-ethylpyridine-3,4-diamine with solubility in DMSO of 50 mg/mL is used in medicinal chemistry assays, where it provides reliable compound dissolution for screening. Molecular Weight 244.07 g/mol: 5-bromo-N4-ethylpyridine-3,4-diamine with a molecular weight of 244.07 g/mol is used in drug design studies, where it facilitates accurate stoichiometric calculations. Residual Water Content <0.5%: 5-bromo-N4-ethylpyridine-3,4-diamine with residual water content less than 0.5% is used in moisture-sensitive reactions, where it maintains reaction integrity and prevents hydrolytic degradation. |
Competitive 5-bromo-N4-ethylpyridine-3,4-diamine prices that fit your budget—flexible terms and customized quotes for every order.
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The world of fine chemicals stays dynamic, constantly branching into specialty areas that tackle modern challenges in pharmaceuticals, materials, and research applications. As a manufacturer, we stand on the ground floor of this process, transforming pure science into practical compounds that open new doors for our clients. One such product is 5-bromo-N4-ethylpyridine-3,4-diamine. This molecule, drawing from the pyridine family yet thoughtfully modified, has caught the attention of both researchers and formulation scientists for good reason. Our hands-on experience in producing this compound gives us a unique perspective on its value, best uses, and differences from the more common building blocks available today.
Let’s talk about why chemists wanted this molecule in the first place. 5-bromo-N4-ethylpyridine-3,4-diamine steps apart from basic pyridine derivatives thanks to selective substitution at the 5-position with a bromine atom and an ethyl group linked to the N4 position. It’s not just a matter of adding bulk or tweaking polarity — these changes significantly influence both reactivity and downstream synthetic flexibility. The bromo group in particular opens doors for Suzuki or Buchwald coupling, which remains standard practice in assembling complex heteroaromatic frameworks. The N4-ethylation moderates hydrogen bonding and imparts a distinct solubility profile, making the compound more approachable in a broader range of solvents.
With a tight melting range and well-characterized appearance, our batches run finely consistent, bearing a pale hue and grain size tailored for laboratory handling. We maintain rigorous standards in water content, purity, and trace metal levels, employing advanced analytical controls after each crystallization batch. As the team responsible for reaction monitoring and quality assurance, we know exactly how each step upstream and downstream affects the end product — and we’re ready to troubleshoot, scale, or adapt as needed to fit clients’ evolving demands.
This molecule continues to find use in medicinal chemistry, where scaffold hopping and fragment elaboration stake claim in new patents and therapies. Many drug-discovery programs require rapid access to intermediates like 5-bromo-N4-ethylpyridine-3,4-diamine. On the bench, our clients deploy it in cross-coupling sequences meant to stitch together diverse aromatic systems. Its dual functionalization pattern — bromine for activation, diamine for tuning hydrogen bonding — unlocks reaction routes that simply aren’t available with unsubstituted pyridine or less elaborate diamines.
Scientists researching kinase inhibitors and other protein–ligand modulators take advantage of both the base-labile ethyl group and the proximity of amine groups, which allows for selectivity against target enzymes. That bromo handle works beautifully in late-stage diversification, a feature that cuts down steps during route scouting. Our technical teams frequently exchange notes with customers on these protocols, optimizing yields and sharing best practices that come straight from the production floor, not marketing decks.
Beyond drug discovery, we watch this compound appear in custom materials, especially in electronic or sensor research labs. The bromine’s presence invites late-stage coupling with sp2 carbons, and the amine functionality lends itself to surface immobilization or polymer extension. This flexibility keeps it in steady demand, especially among university research groups and smaller specialty firms who do not always work from “off-the-shelf” catalogs. Our direct experience with these end-users has shaped the way we package, label, and deliver the product — we don’t ship vague lots or ignore special handling requests.
Years in the business made clear that being just “good enough” doesn’t hold up in this niche. Every lot of 5-bromo-N4-ethylpyridine-3,4-diamine is tracked from raw material to packed drum. We source our starting pyridine rings from upstream partners who agree to full traceability and provide documentation for all critical input materials, down to the carriers and solvents. Purity isn’t a checkbox, it’s our main value proposition: we employ HPLC, GC-MS, and NMR to confirm structure and quantify trace contaminants. There’s no trade-off between efficiency and safety either. Our colleagues on the synthesis line use engineered controls, not just PPE, to maintain consistent working conditions.
Fresh eyes at the reactor catch what automated systems can’t: the faintest color shift, the way a cake filters, the difference in the grind between batches. Our quality teams perform both in-process checks and end-point validation; if something slides outside spec — yield, melting point, or spectral integrity — we review every piece before product heads for packaging. For waste management and regulatory alignment, our compliance officers oversee each disposal procedure and maintain up-to-date documentation for both our own auditing and any required external inspections. These lines of accountability hold our customers’ trust, not just paperwork.
5-bromo-N4-ethylpyridine-3,4-diamine isn’t an everyday commodity. Plenty of pyridine derivatives lack the reactive bromo “handle,” restricting their usefulness for advanced coupling. Other diamines in this class may carry methyl, isopropyl, or bulkier side chains instead of a simple ethyl. The ethyl attachment here offers a sweet spot: not too sterically hindered, not too volatile in downstream chemistry, and it doesn’t invite overalkylation or side reactions common with more reactive alkyl groups. Purified correctly, it avoids the smell and discoloration issues notorious to overhandled pyridines.
From the seat of the reactor, this difference means higher batch consistency and fewer headaches with purification. Our process leads avoid the temperature swings that scorch delicate groups and prevent bromine loss by working under carefully managed atmospheres. Customer chemists mention that competing products often falter in yield or handling after a few months on the shelf. We tackle this by refining stabilization and storing bulk material in inert packaging, which we developed after fielding early feedback from our partners. It isn’t enough to tick off an entry on a catalog. We let our production philosophy — hands-on troubleshooting, careful raw material selection, honest communication about shelf-life and handling — guide each step.
Manufacturing specialty pyridine derivatives isn’t a simple repeat of textbook steps. Lab syntheses and scale-up conditions can surprise even seasoned chemists. Batches of 5-bromo-N4-ethylpyridine-3,4-diamine relied on systematic refinement — from controlling bromination selectivity, to suppressing unwanted side-products, and dealing with the heat sensitivity of the amine groups. The ethylation stage demands careful stoichiometry; too much alkylating agent leads to messy mixtures, too little, and we chase down low yields. The filtration of these batches, too, takes patience: under-vacuum drying can sap away volatile components or produce annoying fines that cloud up final product purity.
Over the years, we adopted trickles of continuous feedback from the floor. Chromatography protocol changes, chelation of trace metals, even the grade of filter papers — every adjustment ties directly to minimizing downtime and maximizing end-use utility for our customers. We abandoned certain solvent systems after seeing the impact these choices had on long-term stability, and we never shy away from investing in new analytical techniques if they promise a tighter spec. Beyond technical work, the training we provide to new technicians holds the rest of the process together. People, not just machines, catch the weird signals in a batch that a spreadsheet misses.
Relationships with end users go much deeper than just receiving an order sheet and shipping a drum. The scientists developing new chemical entities, building materials for electronics, or crafting novel catalysts want more than a supply guarantee. They ask questions that only a manufacturing team steeped in real product history can answer: has this lot had issues with dimerization? Is there any shift in NMR peaks after storage? Which impurities might pop up, and what do they look like in UPLC? We field these questions every week. Sometimes our technical experts cross-check a client’s application test data with our internal batch records, tracing an inconsistency back to a particular piece of starting material.
This back-and-forth lets us learn from our clients, shaping our own process improvements, and also alerts us to shifting priorities in the marketplace. For instance, as regulatory requirements tighten or new green chemistry protocols roll out, our chemists and compliance leads review handling and waste streams with fresh eyes. We push for solvents and reagents with higher recovery rates, and adjust our hazard communication to stay current. Trust, for us, grows from these direct exchanges: when we know how a product performs “in the wild,” we can eliminate annoyances faced by formulation chemists — and we hear about it fast if something doesn’t measure up.
The growing demand for cross-coupling partners and late-stage derivatization intermediates continues to influence how we manage both small and bulk manufacturing runs. More labs want smaller, fresh-packed quantities to reduce exposure and waste. In response, we introduced split-lot packaging, allowing for maximum flexibility while protecting the material from moisture or atmospheric degradation. Some groups require tailored particle sizing for automated synthesis equipment, which prompted us to invest in better grinding and sieving technology. The requests from drug discovery teams for annotated impurity profiles led us to publish added data, going far beyond the minimum required for sales.
We saw issues arise from tricky supply chains and forecasted raw material gaps, particularly around brominating reagents or specific solvents. We tackled these head-on by building deeper inventories of critical inputs and locking in supplier agreements with performance-based penalties. Our experience in chemical sourcing taught us that forward planning and honest communication with partners beats last-minute patchwork fixes. By anticipating logistical pain points, we keep our clients working without pause, no matter the market swings or regulatory hiccups.
No manufacturer escapes new hurdles, whether stemming from raw material shortages, transportation bottlenecks, or shifting safety standards. With 5-bromo-N4-ethylpyridine-3,4-diamine, the greatest challenge remains consistent quality, even as demand shifts or upstream costs wobble. To address this, we built small, scalable process units designed for quick switchover between products. This lets us slot in shorter runs without contamination and respond faster to specialty requests, especially for “off-cycle” needs from longstanding customers.
Waste handling also gets constant attention. By refining our collection, neutralization, and recycling of by-products, we stay in line with national and regional compliance regimes. Our labs now run life-cycle assessments on solvents and reagents, searching for chances to reduce environmental impact without sacrificing output or customer value. In our experience, sharing real numbers with clients about recycled materials earns their confidence — it’s no longer just a “nice to have” message.
Experience in chemical manufacturing teaches that trust is never built through glossy pages or vague promises. Working with 5-bromo-N4-ethylpyridine-3,4-diamine every day, we recognize that clients value consistency, transparency, and technical backup. Unlike traders or bulk distributors, our team tracks every stage from raw input to finished product, learning from each challenge and sharing these lessons with those who depend on our materials’ reliability. Being on the factory floor and speaking with users day in and out gives us the chance to tweak, improve, and stand behind every shipment in a way that catalog stock simply can’t match.
This approach lets us find new efficiencies, push analytical rigor, and invest in machines and people who make a real difference when the unexpected pops up. From basics like clean packaging and customer support to more advanced topics — trace impurity management, handling stability, or collaborative process troubleshooting — it’s this direct, engaged relationship that sets our product apart. In the world of specialty chemicals, real value shows itself when the job is tough, deadlines are tight, and everything rides on the reliability of each component. That’s the environment where experience counts, and that’s where we deliver.