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HS Code |
174319 |
| Chemical Name | 2-Amino-3-bromo-5-(trifluoromethyl)pyridine |
| Cas Number | 552311-68-1 |
| Molecular Formula | C6H4BrF3N2 |
| Molecular Weight | 243.01 g/mol |
| Appearance | White to off-white solid |
| Melting Point | 48-52°C |
| Smiles | C1=C(C=NC(=C1N)Br)C(F)(F)F |
| Inchi | InChI=1S/C6H4BrF3N2/c7-4-3(6(8,9)10)1-2-12-5(4)11/h1-2H,(H2,11,12) |
| Storage Conditions | Store at 2-8°C, dry place |
| Solubility | Soluble in DMSO, insoluble in water |
| Pubchem Cid | 21931247 |
| Synonyms | 2-Amino-3-bromo-5-(trifluoromethyl)pyridine; 3-Bromo-5-(trifluoromethyl)pyridin-2-amine |
As an accredited 2-Amino-3-bromo-5-(trifluoromethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 25g bottle of 2-Amino-3-bromo-5-(trifluoromethyl)pyridine arrives in an amber glass vial with a tamper-evident screw cap. |
| Container Loading (20′ FCL) | Container loading (20′ FCL) for 2-Amino-3-bromo-5-(trifluoromethyl)pyridine ensures secure, moisture-proof drum packaging for bulk chemical transport. |
| Shipping | 2-Amino-3-bromo-5-(trifluoromethyl)pyridine is shipped in tightly sealed containers to prevent moisture and contamination. It is classified as a hazardous material and must be handled according to relevant regulations. The substance is typically shipped with appropriate labeling, accompanied by safety documentation, and protected from extreme temperatures and physical damage during transport. |
| Storage | Store 2-Amino-3-bromo-5-(trifluoromethyl)pyridine in a tightly sealed container in a cool, dry, well-ventilated area, away from direct sunlight, moisture, and incompatible substances (such as strong oxidizers or acids). Keep the chemical at ambient temperature and avoid sources of ignition. Follow standard laboratory safety protocols and local regulations for handling and storage of hazardous substances. |
| Shelf Life | 2-Amino-3-bromo-5-(trifluoromethyl)pyridine remains stable for at least 2 years when stored in a cool, dry place. |
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Purity 98%: 2-Amino-3-bromo-5-(trifluoromethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high-yield and reproducible reaction outcomes. Melting Point 75°C: 2-Amino-3-bromo-5-(trifluoromethyl)pyridine with a melting point of 75°C is used in custom organic synthesis, where it enables controlled thermal processing and minimizes decomposition risk. Moisture Content <0.5%: 2-Amino-3-bromo-5-(trifluoromethyl)pyridine with moisture content below 0.5% is used in heterocyclic compound manufacturing, where it prevents unwanted hydrolytic side-reactions. Particle Size <100 μm: 2-Amino-3-bromo-5-(trifluoromethyl)pyridine with particle size under 100 μm is used in fine chemical production, where it allows enhanced mixing and dissolution rates. Stability Temperature up to 120°C: 2-Amino-3-bromo-5-(trifluoromethyl)pyridine with stability temperature up to 120°C is used in high-temperature catalytic coupling, where it maintains molecular integrity and consistent product quality. Molecular Weight 257.01 g/mol: 2-Amino-3-bromo-5-(trifluoromethyl)pyridine of molecular weight 257.01 g/mol is used in drug design research, where accurate mass facilitates precise formulation and structural analysis. |
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Years of crafting and refining heterocyclic compounds have taught us that every molecule we produce tells a story about the challenges and ambitions of chemists in industries around the world. 2-Amino-3-bromo-5-(trifluoromethyl)pyridine stands out among pyridine derivatives. Not just because the structure is a mouthful, but because bringing this compound to a high level of purity and consistency takes real experience at the bench.
Here’s a molecule with a clear signature: a trifluoromethyl group at the 5-position, a bromine at the 3-position, and an amino group at the 2-position of the pyridine ring. The arrangement might sound mundane if you’ve never had to deal with sensitive substituents and spirited reactivity, but this precise architecture is deliberate. Chemists reach for this flavoured pyridine when they need a building block that offers both electron-rich and electron-deficient handles—each group tweaks reactivity and allows for transformations that simpler molecules can never deliver.
We control every step of the synthesis, from reagent choice to crystallization. Many compounds with halogen and trifluoromethyl substitutions struggle with byproduct formation or overbromination, especially during scale-up. Our team spent years troubleshooting side reactions with pyridine substrates, repeatedly running pilot batches, then analyzing impurities by LC-MS and NMR. This work paid off. We routinely achieve assay values at or above 98.5% by HPLC, measured batch after batch, because we make adjustments in real time. We never trust to “batch averages” alone. If a run drifts, we catch it in process and rework or discard, not simply blend. This consistency isn’t marketing—our downstream partners in pharmaceuticals and agrochemicals rely on these guarantees.
We see this compound in everything from research labs to early-phase drug development. The electron-withdrawing trifluoromethyl group at the 5-position isn’t just for looks—it changes the electron density in the aromatic ring, affecting nucleophilic and electrophilic substitution patterns. The amino group at the 2-position opens sites for acylation, amidation, or Suzuki-type couplings, without too much steric hindrance. The bromine at the 3-position acts as a versatile handle for cross-coupling reactions—all crucial for medicinal chemistry teams chasing new scaffolds.
This molecule supports work on kinase inhibitors, antiviral leads, and experimental pesticides. Researchers tell us that intermediate stability makes scale-up more straightforward than with similar analogs, especially those lacking the electron-poor trifluoromethyl or with halogen atoms at less favorable positions. More than once, we’ve helped a client troubleshoot intermediates by tweaking synthetic routes, only to find that our version of 2-amino-3-bromo-5-(trifluoromethyl)pyridine filled a gap that nothing else did.
In this space, small shifts in substitution patterns can mean big changes in yield, crystallization, and downstream activity. Compare with 2-amino-5-trifluoromethylpyridine, which lacks the bromine. The absence of the bromine limits late-stage functionalization, especially where a direct Suzuki-Miyaura cross-coupling is desired. Or consider the 2-amino-3-chloro-5-(trifluoromethyl)pyridine analog. The chloro group is less reactive than bromo for palladium-catalyzed cross-couplings—most synthetic chemists have learned this lesson the hard way, wasting precious days optimizing conditions with less cooperative leaving groups. Adding a bromo group, as in our product, lightens the load.
These details matter more than most realize. A process route failing at 20-gram scale because a Cl derivative refuses to couple means missed deadlines, lost material, and repeated meetings with process chemists. By using our 2-amino-3-bromo-5-(trifluoromethyl)pyridine, teams can cut out lengthy protection/deprotection cycles or sidestep multiple halogen exchange steps, ultimately pushing more candidates into screening.
Most commercial requests ask about physical form and purity, but lab-scale users care just as much about batch consistency and analytical data. We routinely offer the product as a white or off-white crystalline powder. Moisture content stays below 0.5% by Karl Fischer titration, as verified during QC release. Residual solvents fall within the limits demanded by ICH Q3C guidelines, and we keep a close eye on halogen content, since any deviation can alter downstream reactivity or cause surprise byproducts in bioassays.
Aromatic aminopyridines with halogen and trifluoromethyl substituents always demand careful handling. Our operators wear proper PPE and control airborne particles during weighing and transfer, especially once batches reach kilogram scale. Dust is minimized by controlling humidity and using appropriate dust collection systems, not just fume hoods. We’ve seen firsthand the importance of thorough training; new staff always shadow during their first runs to learn glove technique and bench setup. Safety data is baked into every batch record, not relegated to generic binders.
One important lesson: do not store open samples in humid environments. Even our high-purity batches can hydrolyze at the amino group over months if exposed. Once, a client reported performance drop in an ongoing screen after converting a kilogram from our supply. Investigation showed long-term storage in an office drawer, rather than the suggested sealed, desiccated container. We replaced the material, but it drove home the point. Proper storage keeps quality consistent, and we always include these instructions because too many synthetic efforts falter on overlooked details.
We take pride in direct relationships with end-users. Rather than filtering requests through layers of sales reps, we talk chemistry with customers and troubleshoot their problems. Some researchers want a larger particle size for easier filtration; others need microfine batches for automated dispensing. We adjust crystallization or grinding protocols as needed, not forcing a one-size-fits-all model. Several clients report that our product dissolves more readily in DMF or DMSO compared with competitors, likely owing to tighter control of process impurities and residual water. One pharmaceutical partner shifted their standard process after realizing our version gave sharper chromatographic peaks and improved downstream reaction efficiency.
Feedback isn’t always about performance in the flask. Some teams appreciate our documentation, including analytical certificates that detail every relevant parameter, not just the bare minimum. Years ago, we decided to include NMR, HPLC, and MS spectra as part of every batch package, after hearing frustration from a biotech group who had to chase down suppliers for basic structure confirmation. Our goal is always to make the chemist’s job easier, whether that means troubleshooting a reaction or supplying paperwork for regulatory filings.
People often ask how our 2-amino-3-bromo-5-(trifluoromethyl)pyridine differs from bulk material sourced online. The answer always comes back to attention in both the lab and paperwork. Take, for instance, batches from unknown producers—our analytical team routinely sees differences in trace impurity profiles, even when “purity” numbers look similar on certificates. Impurity carryover can cause subtle but significant shifts in yields or physicochemical properties, especially in demanding applications. Last year, a global life sciences company approached us after repeated failures with a lower-cost alternative. Side products in their process were traced back to unknown contaminants in a cheaper batch. After switching to our product, the process ran as intended, with fewer filtration issues and better isolation.
We always invite technical audits. Visitors can review our documentation, walk the site, inspect equipment, and see our material as it is produced. This keeps us accountable; any recurring issue gets flagged and addressed quickly. No faceless warehouse, no answerless web forms—just chemists, process managers, and quality assurance working alongside each other.
Modern chemical design hinges on access to reliable building blocks. In the race to optimize a new drug or agrochemical lead, being able to quickly derivatize a pyridine ring speeds SAR cycles and eliminates unnecessary delays. The unique arrangement of functional groups in 2-amino-3-bromo-5-(trifluoromethyl)pyridine means chemists can explore a diverse set of transformations: Suzuki coupling at the bromine, amidation at the amino, or targeted modifications at the ring. No need for disconnection strategies that waste precious starting materials or produce hard-to-separate byproducts.
In academic labs, students have used our material for transition metal-catalyzed C–N bond formation, as well as in heterocycle construction via cyclocondensation. Reports from several university groups highlight improved reactivity with our product compared to similar compounds with different substitution patterns. Pharmaceutical customers often use our compound in creating fragment libraries focused on fluorinated scaffolds, since trifluoromethyl groups play a key role in tuning metabolic stability and bioavailability.
Working at the bench isn’t glamorous, and every synthesis throws a few surprises. Over time, we’ve found that focusing on data improves not just our yields, but our customer relationships. For each lot, analytical instruments double-check the spectrum: sharp singlets in NMR, clear mass peaks, and consistent integration in HPLC trace. By tracking shifts in these readouts over dozens of batches, we spot small drifts early, often before they affect reactivity.
Our QC chemists meet regularly to review records, linking problems to specific steps or reagents. For instance, we once detected a persistent side-product after a supplier changed the grade of an upstream brominating agent. Identifying the shift, tracing it back, and updating our supplier list made a bigger impact than any single process modification. Sharing these real-world examples builds trust, internally and externally.
True security in procurement comes from stable supply and open communication. No one benefits from holding up a development team because a crucial compound is backordered. We maintain buffer stock and scale batches in anticipation of seasonal fluctuations in demand. If a run needs to move from grams to kilograms, we support clients with documentation, batch records, and, if needed, custom packaging. Pharmaceutical teams appreciate that full traceability and regulatory documentation are part of every shipment, not exceptions for “VIP customers.”
Each consignment leaves our facility in sealed, inert-gas-flushed containers. Every batch passes through documented sampling, reserve retention, and full analytical confirmation before delivery. If a customer reports an issue, the same batch reserve is analyzed by both our team and, if requested, a third-party lab. Transparency pushes our staff to higher standards and gives our customers real peace of mind.
As the pressures on research teams and production chemists intensify, the need for responsive, robust suppliers grows. We know that a single sluggish step in a multistep synthesis can spell trouble, and that’s why real batches, with real batch records and analytical support, form the backbone of everything we supply. The users of our 2-amino-3-bromo-5-(trifluoromethyl)pyridine aren’t just buying a chemical; they’re seeking a partner in research—a team able to troubleshoot, adapt, and deliver without fuss.
Whether it’s scaling up for pilot plant trials or shipping fresh material to a research lab on a tight deadline, our approach stays rooted in years of hands-on experience. We’ve learned, sometimes the hard way, that success comes from collaboration, transparency, and a relentless focus on quality—qualities that matter far more than technical jargon or brochure-speak.
Continuous improvement drives our operations. Quarterly reviews pull in feedback from all corners—lab staff, quality teams, and customers—each pushing us to fine-tune process steps or documentation. Sometimes, improvements come from the shop floor: a technician’s suggestion to swap out a filter media or a chemist’s insight on adjusting the rate of addition for a cleaner reaction. Sometimes, changes are customer-driven, such as special packaging or batch documentation for regulatory review. We treat each request as a new opportunity to refine both product and service.
Partnership with labs, universities, and industrial users means we’re always updating our knowledge about new applications, process tweaks, and regulatory expectations. Staying nimble helps us meet the evolving needs of the synthesis community, whether that’s improving analytical capabilities, expanding documentation, or developing better storage logistics.
Sustainability isn’t just a buzzword in our facility. Every decision about process conditions, solvent recovery, and waste minimization gets reviewed by our safety and environmental team. Where possible, we redesign synthetic steps to reduce hazardous byproducts and recover solvents—one reason our local regulators have given us high marks during inspections. Regular audits keep our environmental impact in check and ensure that every batch, from conception to shipping, meets not only the requirements of our customers but also the standards of our community.
As global regulations grow tighter, especially in pharmaceuticals and crop science, our documentation and internal controls allow customer teams to navigate audits smoothly. We support them with full traceability, detailed impurity profiling, and responsive communication in the face of changing guidelines.
2-Amino-3-bromo-5-(trifluoromethyl)pyridine stands apart, not only as a tool in the chemist’s kit but as a product carrying the hard work and discipline of every person involved in its creation. Our hands-on approach, persistent troubleshooting, and direct relationships with users ensure that each shipment supports research and production goals—not just with promises, but with data and action. As chemistry advances and new challenges appear, we remain committed to supplying material that combines technical reliability with a sense of partnership and responsibility. Every gram reflects our experience, attention to detail, and respect for the users who trust us to support their breakthroughs.