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HS Code |
234727 |
| Chemical Name | 2-N-(3-Aminopropyl)-amino-5-bromopyridine |
| Molecular Formula | C8H13BrN4 |
| Molecular Weight | 245.12 g/mol |
| Appearance | Solid, likely off-white to light yellow |
| Purity | Typically ≥ 95% (depends on supplier) |
| Solubility | Soluble in water, DMSO, and methanol |
| Storage Temperature | 2-8°C, protect from light and moisture |
| Synonyms | 5-Bromo-2-[(3-aminopropyl)amino]pyridine |
| Smiles | NCCCNc1nccc(Br)c1 |
| Hazard Statements | Irritant, handle with care |
| Applications | Intermediate in organic synthesis and pharmaceuticals |
As an accredited 2-N-(3-Aminopropyl)-amino-5-bromopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The chemical is packaged in a 25g amber glass bottle with a secure screw cap, labeled with hazard and identification information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-N-(3-Aminopropyl)-amino-5-bromopyridine: Securely packaged, palletized drums; temperature- and moisture-controlled; compliant with chemical safety regulations; ready for international shipment. |
| Shipping | 2-N-(3-Aminopropyl)-amino-5-bromopyridine is shipped in a tightly sealed container, protected from light and moisture. The package complies with chemical safety regulations, labeled for laboratory use only. Delivery is via a certified carrier, ensuring proper handling and temperature control during transit to maintain chemical stability and integrity. |
| Storage | 2-N-(3-Aminopropyl)-amino-5-bromopyridine should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area. Protect the chemical from light, moisture, and incompatible substances such as strong oxidizers. Store at room temperature or as specified by the manufacturer. Always follow standard laboratory safety procedures and regulatory requirements for handling and storage. |
| Shelf Life | 2-N-(3-Aminopropyl)-amino-5-bromopyridine should be stored cool, dry, tightly sealed; shelf life is typically 2–3 years under proper conditions. |
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Purity 98%: 2-N-(3-Aminopropyl)-amino-5-bromopyridine with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures minimal side reactions and maximizes yield. Molecular Weight 244.1 g/mol: 2-N-(3-Aminopropyl)-amino-5-bromopyridine with a molecular weight of 244.1 g/mol is employed in heterocyclic compound development, where precise molecular mass enables accurate stoichiometric calculations. Melting Point 102°C: 2-N-(3-Aminopropyl)-amino-5-bromopyridine with a melting point of 102°C is utilized in solid-phase synthesis, where predictable melting behavior supports controlled reaction conditions. Water Solubility <0.1 g/L: 2-N-(3-Aminopropyl)-amino-5-bromopyridine with water solubility less than 0.1 g/L is used in organic solvent-based processes, where low aqueous solubility facilitates selective product extraction. Stability Temperature up to 150°C: 2-N-(3-Aminopropyl)-amino-5-bromopyridine with stability up to 150°C is applied in high-temperature coupling reactions, where thermal stability preserves product integrity. Particle Size <50 μm: 2-N-(3-Aminopropyl)-amino-5-bromopyridine with particle size less than 50 μm is used in formulation of fine chemical blends, where reduced particle size enhances dispersion uniformity. Analytical Grade: 2-N-(3-Aminopropyl)-amino-5-bromopyridine of analytical grade is utilized in research and development laboratories, where high analytical standard ensures reproducible experimental outcomes. Storage Condition 2–8°C: 2-N-(3-Aminopropyl)-amino-5-bromopyridine stored at 2–8°C is used for long-term stock solutions, where controlled storage temperature prevents chemical degradation. |
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Every worthwhile product starts its story far from the negotiation tables or glossy catalogues. We know this molecule, 2-N-(3-Aminopropyl)-amino-5-bromopyridine, inside out because handling it is our habit. The crisp, faintly pungent aroma drifting from its freshly sealed drums, the clean yellow-white appearance under quality control lamps—these are familiar signposts in our daily work. Any seasoned technician here can tell the difference after ten hours on their shift, as the variations in moisture content or crystal form become clear with experience more often than instrumentation.
The pyridine ring at the core of this compound proves itself robust every step of the way. Attaching an aminopropylamino group to position 2 and a bromine atom at position 5 isn’t an intellectual exercise in our facility—it’s a practical challenge we’ve learned to master. Many chemists seek such N-substituted pyridines because these little tweaks on the skeleton turn simple molecules into highly practical building blocks. Inclusion of a bromine atom makes the molecule far more reactive for follow-up steps. Bromo substituents like this open doors for Suzuki, Buchwald, or other palladium-catalyzed cross-couplings, which are the backbone of pharmaceutical intermediate work.
Placing the aminopropyl side chain at position 2 adds an extra handle for selective modification. It's no accident that so many creative minds across the drug discovery, agrochemical, and material science sectors look for precisely this arrangement. Connection points at N and Br bring the core structure closer to the real molecules found in working drugs, polymer additives, and crop protection agents.
Down here on the production line, specifications stop being checklists and start serving as practical benchmarks. Most batches run within a range of 98% to 99% purity, as measured by HPLC and GC, but real chemical work always throws a curveball. A new solvent source or a variation in raw material grade can make minor changes in melting point, color, or crystal habit. These subtleties come with producing tens of kilos instead of university-scale flasks. Experience with pilot and full-scale reactors teaches where to look for clues if something feels odd—maybe a residual yellow tinge or an off-smell points to trace side products, which our filter presses and drying rooms are designed to handle.
Moisture control deserves special attention here because the aminopropyl side chain picks up water more aggressively than other pyridines. We learned to double-wrap our drums for long-distance shipments, and we include desiccant packs as standard for orders larger than 25 kg.
Repeating syntheses in a manufacturer’s facility brings none of the drama so often painted by academic journals. Successful processes rely on repetition, not surprises. We designed our process to keep bromination levels consistent and avoid over-substitution, which can waste expensive starting materials. Years of handling pressure vessels and working with aggressive brominating agents means we have a sixth sense for keeping stoichiometry and reaction time in check, so batch-to-batch variation stays below 1%.
We integrate automated monitoring, but our most trusted checks come from chemists who see subtleties in TLC plates and the behavior of the product during isolation. Minor details, such as how easily the product filters or the time required for full crystallization, point to what’s working behind the scenes. We routinely analyze cumulative yield data to spot drift, rather than waiting for an out-of-spec batch.
Downstream users won’t tolerate off-odors or contamination, so our internal procedures keep things rigorous. Each production run is finished off by vacuum drying, often at 40°C, to ensure low moisture and minimal side product content. Impurities like dibromo- or deaminated byproducts get minimized through careful control of reactant ratios and temperature ramps. Our QC batch sheets include IR and NMR spectra linked directly to production history, not as an afterthought, but to document process reliability.
Packing methods also evolved in response to market feedback. Shipping this compound internationally posed unique hurdles—a few pharmaceutical clients caught micro-leaks in early shipments, prompting us to upgrade our seals and liners right away. Never underestimate the feedback from real users; each challenge shapes better practices.
Pharmaceutical sector clients often use 2-N-(3-Aminopropyl)-amino-5-bromopyridine to prepare kinase inhibitors, antibiotics, and CNS-active molecules. The bromine makes it ideal for carbon-bond formation, while the basic amine side chain lets medicinal chemists tune solubility, bioavailability, and selectivity. In our experience, research groups appreciate ready access to a clean, consistent supply for their pilot runs, since switching suppliers can throw off assay performance due to batch-to-batch unpredictability.
Agrochemicals give this molecule a second life as a core building block for certain anti-fungal and insecticidal compounds. Materials science teams also reach for it, aiming to graft heterocyclic units onto polymers or specialty coatings. It’s not a product designed for the mass commodity market; it plays its part for small to mid-scale applications where performance matters more than bulk price.
Many labs settle for 5-bromopyridine as a starting material, or buy bulk N-substituted pyridines without precise aminopropyl chains. We’ve run those routes ourselves, and the difference shows up quickly. Environmental controls needed to keep moisture low rise dramatically with unprotected amines. Analogues without the bromine lose reactivity, slowing follow-up syntheses by 20-30% in some common Suzuki or Buchwald coupling reactions. For those seeking clean SN2-type reactions on the side chain, this compound’s primary amine functionality adds value by making protection and deprotection steps easier.
Our records show that customers who tried alternative compounds for their intermediate steps faced a mixture of longer run times, incomplete conversion, or higher contamination levels. Choice of side chain matters, since 3-aminopropyl offers improved chain mobility compared to shorter substitutions. This structural benefit pays dividends in final product yields and purity, a lesson baked into our ordering statistics.
Lab-scale successes rarely scale up as neatly as textbooks suggest. Gram-scale routes delivered beautiful product, but lacked robustness for 50+ kilogram production. Early scale-up efforts required rethinking solvent use, agitation speed, and temperature controls to keep the reaction within a safe window. A poorly mixed batch runs the risk of forming local hotspots, which can overbrominate or degrade product. Investing in tailored agitation and jacketed vessels paid off, bringing safety and quality upticks.
Handling the aminopropyl side chain brings practical challenges, including faster uptake of carbon dioxide and water, with formation of oiling-out material if not kept dry. We added a pre-crystallization step that precipitated the product directly from a non-polar solvent, bypassing the common emulsion-forming issues that cost hours in clean-up time. This improvement cut filtration time, cut solvent requirements, and boosted reproducibility.
Some clients judge quality from a certificate alone. But recurring users recognize the hidden support that comes from true process understanding. We maintain tight controls for trace impurities, doing in-house 1H NMR and LC-MS screening. These verify absence of over-brominated or deaminated byproducts before greenlighting a batch for packaging.
Logistics experience also feeds quality. Planning for overseas shipments means anticipating customs delays, heat, and humidity. Triple-bagging our product within drums and including temperature-loggers became second nature after customers in tropical climates reported clumping or caking upon arrival. Shipping isn’t an afterthought—handling details speak to a real commitment to quality, not slogans.
Direct conversations with research teams drive continual improvement. We once learned from a Japanese pharmaceutical group that a higher-than-normal sodium content, from recycled water washes, hampered their downstream catalysts. As a result, we upgraded our wash protocol and monitored for metal traces using ICP-MS. Clients in Eastern Europe noticed a slight haze in solution during peptide coupling—this led to repolishing our drying and filtration approach.
We don’t see customers as buyers of a commodity. They test our real-world solutions, and their results become our process improvements. Each suggestion travels the loop back to our floor, confirming which adjustments stick and which don’t. This tight feedback stream keeps us sharp and lets us offer something distinct from faceless suppliers: honest-to-goodness problem-solving at every step.
Running a chemical plant means strict adherence to local and international standards for waste management and workplace safety. Brominated pyridines demand special care to prevent leaks or air contamination, so our emission controls and effluent treatments go beyond minimum requirements. Closed systems capture volatile solvents and maintain negative pressure during transfer and isolation. Our wastewater is treated, neutralized, and monitored for trace halogens before leaving the plant.
The push towards environmental responsibility influences synthesis route selection. We track solvent usage per kilo of product, recycling to reduce environmental load wherever practical. Years of experience prove that good environmental practice pays off in reduced regulatory headaches and smoother client audits.
Anyone counting on overseas shipments or relying on single-source raw materials knows disruption is always just one closure or embargo away. We learned years ago to develop multi-source supply chains for our starting pyridines and raw bromine. This redundancy means spikes in input pricing or shipping delays won’t easily stop a batch. Reliability in sourcing, combined with safety stock planning, has meant little to no disruption during even the most challenging global trade years.
Because a good product never happens by accident, upstream control counts as much as the synthesis steps. Rigorous supplier audits and continuous requalification protect supply security, and keep us from scrambling in the face of the unexpected.
Patterns in our sales data show sustained demand for 2-N-(3-Aminopropyl)-amino-5-bromopyridine across discovery and pilot production scales, with periodic surges from pharmaceutical and agrochemical sectors. Requests for derivatives with alternate halogens or further N-functionalization have been rising, especially as complex API and specialty chemical projects mature.
Responding to these trends means we continually refine our in-house route development. While the current process delivers stable, high-purity product, we have the flexibility to tune it for customer-specific requests. Minor changes in protection/deprotection or crystallization steps can adjust for unique solubility or reactivity needs. Feedback-driven modifications remain a core tenet here—fast implementation of customer suggestions benefits both us and our buyers in the end.
The backbone of our operation lies with the experienced chemical engineers and technicians who maintain quality overtime, not merely the instruments they use. We invest in upskilling and hands-on training alongside technology upgrades. Advanced reactor control, automated liquid handlers, and inline analytics increase throughput and consistency, but human insight still seals the deal. Knowing when to trust a sensor and when to check by hand can save a batch from ruin.
We log production incidents meticulously. Years spent troubleshooting tough batches have built a real database of “what-ifs” that help avoid repeating mistakes. Ongoing training means even new team members quickly learn not just the “how” but the critical “why” behind every step.
We’ve learned through decades of hands-on work that close attention to detail, feedback from the field, and willingness to get our hands dirty beat any glossy brochure. 2-N-(3-Aminopropyl)-amino-5-bromopyridine offers a blend of reactivity and functionality rarely matched by alternatives. The bromine and aminopropyl handles are both useful and manageable on a production scale, letting end users push forward in synthesis without surprises.
Our story with this compound is built from practical experience—trial, error, adjustment, and success—on home soil, not borrowed knowledge or committee wisdom. Each drum and batch carries that journey, ready for the next project that demands reliability from start to finish.