|
HS Code |
757867 |
| Productname | 2-Amino-5-Bromo-3-Iodopyridine |
| Molecularformula | C5H4BrIN2 |
| Molecularweight | 298.91 g/mol |
| Casnumber | 887593-87-3 |
| Appearance | Light yellow to brown powder |
| Purity | Typically ≥98% |
| Solubility | Soluble in DMSO, ethanol, and methanol |
| Synonyms | 5-Bromo-3-iodo-2-pyridinamine |
| Smiles | NC1=NC=C(Br)C(I)=C1 |
| Inchikey | JUQQNUBYQHWVJB-UHFFFAOYSA-N |
As an accredited 2-Amino-5-Bromo-3-Iodopyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 10g 2-Amino-5-Bromo-3-Iodopyridine is sealed in an amber glass bottle with a tamper-evident cap and chemical label. |
| Shipping | **Shipping Description:** 2-Amino-5-Bromo-3-Iodopyridine is shipped in sealed, moisture-proof containers under ambient temperature conditions. The chemical is classified as a laboratory reagent, handled with care to avoid exposure or contamination. Ensure compliance with all applicable regulations regarding hazardous materials during transportation. Accompany with a safety data sheet (SDS) and proper labeling. |
| Storage | 2-Amino-5-Bromo-3-Iodopyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from direct sunlight, moisture, and incompatible substances such as strong oxidizers. Store at room temperature and avoid extreme temperature fluctuations. Properly label the container and ensure that only authorized, trained personnel have access. Follow all relevant safety and regulatory guidelines. |
| Purity 98%: 2-Amino-5-Bromo-3-Iodopyridine with 98% purity is used in pharmaceutical intermediate synthesis, where high purity ensures reduced side-product formation. Melting Point 210°C: 2-Amino-5-Bromo-3-Iodopyridine with a melting point of 210°C is used in high-temperature organic reactions, where thermal stability supports complex synthesis processes. Molecular Weight 299.93 g/mol: 2-Amino-5-Bromo-3-Iodopyridine with a molecular weight of 299.93 g/mol is used in drug discovery research, where precise molecular mass facilitates accurate formulation. Particle Size <50 μm: 2-Amino-5-Bromo-3-Iodopyridine with particle size less than 50 μm is used in fine chemical manufacturing, where enhanced reactivity and dissolution rate improve process efficiency. Stability Temperature up to 100°C: 2-Amino-5-Bromo-3-Iodopyridine stable up to 100°C is used in catalyst preparation, where maintained integrity at elevated temperature ensures product reliability. Water Content ≤0.5%: 2-Amino-5-Bromo-3-Iodopyridine with water content ≤0.5% is used in moisture-sensitive synthesis, where low water levels prevent hydrolysis and degradation. HPLC Assay ≥99%: 2-Amino-5-Bromo-3-Iodopyridine with HPLC assay ≥99% is used in analytical reference standards, where superior purity allows for exact quantitative analysis. Solubility in DMSO 20 mg/mL: 2-Amino-5-Bromo-3-Iodopyridine with solubility in DMSO at 20 mg/mL is used in biological screening assays, where good solubility enhances sample preparation consistency. Heavy Metal Content <20 ppm: 2-Amino-5-Bromo-3-Iodopyridine with heavy metal content less than 20 ppm is used in electronics materials, where minimal metal contamination is critical for high-performance devices. Storage Stability 24 months: 2-Amino-5-Bromo-3-Iodopyridine with storage stability of 24 months is used in chemical inventory management, where long shelf life ensures sustained supply and usability. |
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2-Amino-5-Bromo-3-Iodopyridine has been part of our chemical lineup for several years. Its importance keeps growing, with ever more chemists and R&D teams approaching us for procurement advice. Chemists rely on unique, highly functionalized heterocycles to enable their synthetic routes. Among halogenated pyridine derivatives, this molecule remains a favorite for both scale-up projects and early discovery research. Its CAS number is 887973-20-4, and our own batch records have tracked fine-tuning of its properties through every campaign.
Through long experience in heterocyclic manufacture, we’ve found that quality control on 2-Amino-5-Bromo-3-Iodopyridine can’t be left to chance. Our routine scrutiny covers everything from trace metals down to minimal organic impurities. Our typical output exceeds 99% purity by HPLC, thanks to rigid process housekeeping and hands-on lot analysis. Each batch runs through careful crystallization, not just for looks, but to assure solid-state consistency and reproducibility in research settings. This sort of reliability matters when our pharmaceutical partners need trouble-free results in their Suzuki or Buchwald-Hartwig couplings.
Some might think that all pyridine derivatives coming out of Asia or Europe are interchangeable. Our team has seen just how risky that assumption can be. It’s the subtle details that set one manufacturer’s material apart from others—a point often missed until a downstream reaction stalls or a pilot synthesis fails. Our process skips unnecessary purification steps that degrade the amine, and our iodination protocols minimize polyhalogenated byproducts. This hasn’t always been easy; years ago, we struggled with residual copper levels, which proved troublesome for customers pushing into cross-coupling reactions. We analyzed each variable until we hit the right balance of reactivity and cleanliness, maintaining both yield and selectivity batch after batch. There is no substitute for that level of process knowledge.
What draws so many synthetic teams to this intermediate? The short answer: versatility and reactivity. Few building blocks offer such convenient orthogonality on one ring. With both bromine and iodine on the pyridine core, researchers can plan sequential selective couplings—installing different functional groups on each reactive center. The amino group amplifies this further, providing a handle for urea, amide, or heterocycle construction. In our feedback from pharmaceutical customers, this substrate plays well in fragment-based discovery and library diversification, speeding up the design of kinase inhibitors or CNS actives. Not every pyridine offers such flexibility in combinatorial chemistry.
The largest share of our 2-Amino-5-Bromo-3-Iodopyridine output heads straight to pharma development. In the past two years, demand has risen with the trend toward N-heterocycle-rich drug scaffolds. Academic labs dig deep into this class for target exploration, but scale-up requests usually come from process chemistry teams. They value the well-defined identity and minimal impurity profile, since each new impurity can complicate later purification or toxicology work.
We’ve also noticed growing interest among materials scientists, mainly those experimenting with halogenated pyridines as ligands or monomers. One team even shared data on using this compound for the creation of complex polymers with tunable optoelectronic properties. While this segment remains a fraction of overall volume, it points toward new frontiers for the molecule beyond pharmaceuticals.
Our standard offering of 2-Amino-5-Bromo-3-Iodopyridine comes as a free-flowing, pale crystalline powder, packaged in airtight containers that suit both research bench and pilot plant needs. Content remains stable under dry, ambient storage, thanks to the absence of hygroscopic excipients or diluents. Several partners who previously struggled with caking from offshore sources switched over after noticing our material dissolves predictably in DMF and DMSO. Our focus on crystal habit and drying conditions pays off in user experience, not just on paper product claims.
We run routine checks on particle size and residual solvent content. For certain customers, we offer customized milling or sieving to optimize for specific reactors or automated dispensing systems—a detail we developed after troubleshooting customers’ micronization steps. By staying attentive to users’ feedback, we continue refining how we handle and present this compound, beyond batch-specific tweaks.
Pragmatic handling advice comes from the realities of working with halogenated aminopyridines over the years. While the substance does not pose extreme hazards under usual operating procedures, it still calls for careful housekeeping due to its amine functionality and halogen content. Our technical service group keeps detailed processing notes and provides honest, experience-based support for safe transfer, waste management, and compatibility with common solvents.
We also field a steady stream of requests for reactivity data, both from organic chemists and environmental health safety teams. This direct, real-world knowledge stands apart from the generic, templated responses often served up elsewhere. Our records are built on lessons learned in our own facility, tracked through continual closeout and process review, not hypothetical lab-scale assumptions.
It’s not unusual for customers to try out small amounts from multiple suppliers before settling on a partner. Sooner or later, the same questions resurface: Does it dissolve cleanly? Any residual peaks in NMR? Odd smells or unexpected melting behaviors? Those details can tip the scales on a drug’s synthetic route or on a multi-million dollar library screen. Back when we first introduced this product, the consistency between shipments wasn’t where we wanted it. By making incremental improvements—close monitoring of reaction temperature windows, careful tracking of halide equivalents, targeted column chromatography conditions—we shaped a product that meets real-world needs, not just catalog descriptions.
This material doesn’t just slot into a reaction. It sparks innovation in laboratories that count on revisiting procedures over months of research. Reliable, repeatable material frees chemists to pour their time into meaningful synthesis, not troubleshooting impurities or recalibrating routines. During a recent audit by a domestic life-sciences major, our traceability records and lot-by-lot impurity logs passed inspection with zero comments. Years of data give buyers and process engineers confidence that they’re investing in more than a one-off lot.
Many synthetic approaches can start from other halogenated pyridines, but few alternatives provide the same degree of positional selectivity and reactivity. Take 2,6-dihalo- or 3,5-dihalo-pyridines; these molecules miss key handles for functional group divergence that 2-Amino-5-Bromo-3-Iodopyridine delivers. This difference drives more efficient synthetic planning, saving chemists work-arounds and dead-ends.
We’ve worked with teams who attempted to make this intermediate in-house before switching over to our bulk material. We saw their challenges first-hand: unpredictable yields, messy chromatograms, waste streams that stretched disposal budgets. With specialized knowledge in scale-up and halogen handling, we cut down on hazardous reagent use, improved byproduct separation, and brought run-to-run output into a manageable range. The economies of scale and controlled environment produce a consistently better reagent—not just lower cost but a more streamlined workflow at the bench.
Lab managers often call about our repeatability, not just for a single kilo but across years of purchasing. Most customers want to buy once and focus on their chemistry, not product validation. Keeping up this reliability means more than having a list of certifications. We rely on regular team meetings, process audits, and lab-scale pilot reruns so that even rare process drift gets caught early.
Most producers could, in theory, hit high assay content or visual appeal. Our advantage comes from daily engagement and readiness to tune parameters based on feedback, not rigid adherence to a static operating procedure. One long-term partner shared that, after switching to our product, their purification steps run twice as fast and filter plug rates dropped dramatically. Attention to both the obvious and the fine-grained details serves experienced chemists best.
Innovation in the synthetic community never stands still. Our development chemists stay in close touch with leading-edge researchers, offering hands-on support for reaction optimization, scale-up challenges, and analytical questions. Access to the right batch data and extensive application notes puts practical experience behind every shipment. This degree of technical engagement can reduce troubleshooting cycles and expedite timelines for complex projects, whether it’s an early-stage medicinal program or a commercial launch.
Over the years, we’ve seen protocols evolve alongside new catalytic systems. The twin halogens on this pyridine ring react at different rates, allowing chemists to set up sequential functionalizations that other isomers can’t support. Instead of cookbook chemistry, our users can trial new synthetic plans with fewer risk factors because they know their input materials behave as expected. Periodically, specialists from our technical group visit customer sites to observe large-scale runs and gather insights for further improvements.
Every sector has faced disruptions in chemical supply over recent years—regulatory updates, raw material price shifts, logistics hiccups. Our experience is no exception. Maintaining an adequate inventory of such specialized intermediates requires careful forecasting and engagement with trusted raw material partners. We track regulatory status to ensure legal trade, but we also plan ahead to absorb sudden demand bumps, as happens with shifting project priorities in pharma.
Tighter scrutiny over hazardous waste and transport raises new issues, too. Producers with deep process know-how, who invest in cleaner downstream recovery, enable more responsible handling from start to finish. Our investment in sustainable process tweaks—lower solvent usage, improved halogen recycling—feeds back into both cost benefits and environmental targets set by our customers’ procurement teams.
The most enduring lesson we draw from years in this market: open channels make for better-quality chemistry. Regular, detailed feedback from seasoned users, entry-level researchers, and procurement teams helps us learn which batch features matter most—and which slip through the cracks of classic specs. Some customers value visually pristine lots, others chase the sharpest NMR only. We take all this seriously, funneling it back into our planning for the next process update or packing refresh.
Each run strengthens our knowledge on this molecule’s quirks, stability, and reactivity in applied chemistry. Our team keeps a close watch on technical advances, aiming to deliver a product that stays relevant as reaction methods and synthetic targets evolve. Making the right intermediate, in the right way, with open, honest communication—these all fuel better research and faster discovery.
Over the last decade, the expectations from industrial and academic buyers have shifted toward supplier reliability, transparency, and proactive improvement. By tracking and analyzing every run of 2-Amino-5-Bromo-3-Iodopyridine, we stay prepared for the next shift in chemistry trends, regulatory frameworks, or customer requirements. We draw on our historical data to suggest improvements, whether it’s about solvent compatibility, impurity trends, or batch size flexibility. Routine doesn’t rule us; close customer partnerships and a willingness to adapt are at the core of our operation. Keeping this culture alive inspires confidence—so our partners can innovate freely, knowing their critical building blocks are in steady hands.
Many have asked why this intermediate keeps its place in medicinal chemistry and synthesis innovation. It stands out because chemists trust what arrives, and manufacturers know the difference that trust brings in a high-stakes, detail-driven field. That foundation lets researchers build safer, more effective new molecules, with the peace of mind that someone on the supplier side takes their work as seriously as they do.