|
HS Code |
819921 |
| Iupac Name | 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- |
| Molecular Formula | C21H20BrF2N2O2S |
| Molecular Weight | 479.37 g/mol |
| Cas Number | 1256584-76-7 |
| Smiles | CC(C#C[C@@H](CN1=CC=CC=N1Br)Cc2cc(F)cc(F)c2)S(=O)(=O)C |
| Inchi | InChI=1S/C21H20BrF2N2O2S/c1-15(21(3,29(4,27)28)9-10-26)14-13-20-19(22)8-7-18(25-20)12-16-5-6-17(23)11-16/h5-8,11,13,15,26H,9,12,14H2,1-4H3/t15-/m0/s1 |
| Purity | Typically ≥98% |
| Appearance | White to off-white solid |
| Storage Temperature | 2-8°C (refrigerated) |
| Solubility | Soluble in DMSO, partially soluble in methanol |
| Optical Activity | Stereochemistry: (αS)-configuration |
| Hazard Statements | May cause skin and eye irritation |
As an accredited 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 1 gram, labeled "2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-… [αS]," with hazard warnings. |
| Container Loading (20′ FCL) | 20′ FCL (Full Container Load) loaded with securely packaged `2-Pyridinemethanamine, 3-bromo…` drums, following chemical safety and segregation standards. |
| Shipping | This chemical, 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)-, is shipped in accordance with all applicable regulations. It is packaged securely in chemical-resistant containers with appropriate labeling, accompanied by a Safety Data Sheet (SDS), and may require temperature control or special handling during transit. |
| Storage | 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- should be stored in a tightly closed container, protected from light and moisture, at 2–8°C (refrigerated). Ensure storage in a well-ventilated, cool, dry place, separate from incompatible substances such as strong oxidizers, acids, or bases. Proper chemical labeling and secondary containment are recommended for safety. |
| Shelf Life | Shelf life: Typically stable for 2–3 years when stored in a cool, dry place, protected from light and moisture. |
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Purity 98%: 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- purity 98% is used in pharmaceutical intermediate synthesis, where it enables high-yield coupling reactions. Molecular weight 471.30 g/mol: 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- molecular weight 471.30 g/mol is used in medicinal chemistry research, where precise molecular profiling improves lead optimization. Melting point 110–112°C: 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- melting point 110–112°C is used in solid-state formulation studies, where thermal stability ensures integrity during processing. Particle size <50 µm: 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- particle size <50 µm is used in fine chemical blending, where uniform dispersion leads to consistent reaction kinetics. Stability temperature up to 60°C: 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- stability temperature up to 60°C is used in storage and transport scenarios, where chemical integrity is maintained under moderate conditions. Optical purity >99% ee: 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- optical purity >99% ee is used in enantioselective synthesis, where high stereochemical fidelity delivers targeted biological activity. |
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On the floor of our chemical synthesis plant, the pursuit of targeted compounds demands both patience and precision. 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- stands out in our portfolio as a product that reflects not just technical complexity, but years of practical experience responding to the needs of advanced research clients. The chiral purity, the specific substitution patterns on the pyridine core, and the deliberate introduction of functional groups – each step adds layers of challenge. Looking at a bottle of this compound, most might see a long chemical name and a batch code. From our perspective, every gram reflects a set of process decisions and a direct response to real-world hurdles in pharmaceutical discovery and chemical development.
To synthesize a molecule like this at meaningful scale, you can't simply follow a textbook. Each aryl bromide addition brings its own reactivity issues, and the bulky, difluoro-phenyl group means not all reagents behave as planned. Over the years, we've adjusted solvent systems, cooling rates, and purification methods to keep each lot consistent not just in purity, but also in optical characteristics. For researchers chasing a project in kinase inhibition, or developers validating SAR (structure-activity relationship) trends, that αS configuration is essential – so our focus remains delivering reliable chiral enrichment in every run.
Batch after batch, we've monitored melting points, LC-MS signals, and enantiomeric excess. The presence of a methylsulfonyl group at the butynyl position increases polarity and also complicates crystallization. Real-time tweaks in temperature controls and column chemistry have kept us ahead of the drift that so many processes experience over repeated synthesis cycles. Years of GC trace comparisons remind us: it takes more than an SOP pulled from early publications to ensure that a kilogram today behaves as predictably as the pilot gram we made in early trials.
This particular molecule finds its most significant use as an intermediate. Developers and synthetic chemists have employed it to open up new routes in both small molecule drug candidates and specialty functional materials. In our facility, we often receive direct feedback about bottlenecks customers face. Sometimes, it’s an issue with stability during long-term storage. Sometimes, it’s the difficulty of dissolving the compound into application solvents during scale-up. Listening to these stories, we’ve fine-tuned our drying steps and adapted our bottling to reduce atmospheric moisture ingress, keeping both purity and shelf stability in mind.
Few researchers have time to troubleshoot side product formation when a brominated pyridine like this one is at stake in their own benchwork. Curating our purification steps hasn't just minimized downstream complications; it’s shortened the onboarding process for new users. By ensuring the exclusion of even minor isomeric contaminants, users avoid unexplained bioactivity quirks or lost IR signals. The methylsulfonyl handling sets this apart from simpler analogues – it absorbs moisture, so we've moved from classic desiccator strategies to vacuum-sealed packaging. Details like this determine whether a tool compound becomes a true asset or a daily frustration in discovery workflows.
Chemistry is an industry marked by subtlety, and the differences between our 2-Pyridinemethanamine derivative and related structures highlight the importance of process know-how. On paper, replacing a single fluorine or shifting the butynyl substituent may seem trivial. On the floor, those shifts alter reaction rates, polarity, and even shelf life. Some batches in the past taught us the hard way—unstable intermediates or unexpected salt formation pointed out deficiencies in mixing or pH control—and the fixes grew out of direct operator feedback, not simply theoretical optimization.
Complexity isn’t always a virtue. In this product, additional bromination and the introduction of the highly specific 3,5-difluorophenyl group don’t simply add to the name—they create a unique set of electronic properties which our customers leverage in both binding-site investigations and advanced organic electronic applications. Other manufacturers have called us, seeking insight on managing the transition states involved in these late-stage couplings. Over repeated collaboration with both pharma and academic partners, we have developed internal libraries of reaction snapshots. Each shows the impact of subtle process changes, and we share those learnings wherever possible to raise the standard across the field.
Having worked with researchers not just as buyers but also as collaborators, we understand the high pressure that comes with any discovery project. Your program doesn’t wait for supply chain hiccups, and neither does ours. Over time, we've established a batch-release review process that tracks every lot from material sourcing through exhaustive analytical testing. Each chemical comes with a living file of characterization data, not to satisfy a regulatory checkbox, but because we've seen firsthand the setbacks caused by poorly documented provenance. For this advanced pyridinemethanamine, our staff maintains digital archives of spectra and run logs accessible to collaborators who need to align experimental timelines. This practice narrows the risk of redundancy and surprise in shared projects.
Whether the end-use is high-throughput screening or a deep-dive into SAR around cytokine signaling, consistent reagent quality means fewer missed endpoints. We’ve seen graduate projects hinge on reliable batches, and industrial scale-ups rely on the absence of minor contaminants which might otherwise appear at downstream analytical checkpoints. Over the years, feedback loops with our clients have transformed the structure of our own quality management and encouraged deeper transparency. These relationships matter more than any promotional claim.
Few chemical environments feel the pressure of unpredictable reactivity quite like a commercial plant running specialty amines. With this compound, the interplay between the alkyne and the sulfonyl groups calls for careful equipment calibration. We worked through early production runs marked by coking and material loss. Addressing thermal load, we retooled our reactors and re-routed cold solvent quench protocols to manage exotherms without washing away the product. In practice, these changes cut yield loss and made scale-up truly cost-effective—a saving that flows directly through to our research and industrial clients.
Some of the biggest technical headaches come not from synthesis but from handling logistics. Early on, caking issues in this compound forced us to rethink our drying ovens and vacuum application schedules. The result is not just a cleaner product, but a more manageable one for users working under tight deadlines. We’ve replaced older polyseal threads with lined caps for every container, especially for shipments bound for high-humidity environments. From the first inquiry to final shipment, our engineers remain in direct contact with end users to follow up on performance, appearance, and consistency across lots.
In every real research environment, product longevity comes down to protection against oxygen, light, and moisture. For this compound, we've experimented with amber glass, sealed foil sachets, and nitrogen backfilling. The solution we reached—a low-gas-transfer packaging protocol—took continuous observation of returned samples and failed stability tests. Once we saw a yellowing or off-odor, operators tagged the relevant batches, and our packaging group jumped in. Since shifting to our latest line of inert-sealed glass and humidity indicators, complaint rates dropped and requalification batches have all come back clean. Customers notice the difference, especially in multi-month projects involving repeated sampling.
Transport safety isn't an afterthought. Here, the hazard profile remains moderate compared with other arylamines. Through our experience with international clients, we've standardized our MSDS and labeling practices to balance regulatory compliance with clear, field-readable data. Any container leaving our floor includes QR-coded access to up-to-date documents, reflecting any corrective actions or process tweaks since original batch validation.
Knowledge isn’t static in the specialty chemical space. Regular process audits, hands-on cross-training, and a direct line from our production floor to the analytical lab have all prevented repeat errors. One challenge: as molecules become more complex, published literature covers less of the relevant process detail for scaled-up production. To address this, our operators compile “process journals” for each significant compound above lab scale. Entries track not just yields and impurity profiles, but glovebox tips, unexpected colorimetric changes, and real-world safety notes. Sharing those internally has raised everyone’s confidence as we bring on next-generation analogues or scale up client-customized runs.
Working closely with our client partners, we prioritize the transfer of technical insight, not just API units. When project timelines press, a call with our technical support team usually surfaces solutions rooted in small process choices or simple handling adjustments. Over the last year, several partners have credited accelerated project completion to quick access to such process-traceable insight. Our approach makes sure that critical development steps, from lead discovery through early clinical supplies, don’t stub their toes on “trivial” process details overlooked in standard spec sheets. The human factor is what sets us apart from bulk producers or traders with little connection to the bench realities.
Over the last decade, pressure has grown for sustainable practices in specialty chemical production. The molecule in focus reflects that shift. For example, the installation of the methylsulfonyl group previously involved hazardous solvent streams. Through iterative green chemistry brainstorming with both internal process chemists and outside consultants, we reduced the use of chlorinated solvents and cut energy consumption on that step by one-third. This presented early problems; solvent swaps sometimes produced uncharacterized side products. We invested time in additional pilot batches to map unexpected results. The final process yielded not only a cleaner reaction but substantially less chemical waste, benefiting both our cost base and the wider environment.
Staying compliant means monitoring evolving regulations around controlled substance reporting and export restrictions, especially for highly functionalized amines like this one. Documenting chain-of-custody and compliance activities for audits doesn't simply tick a legal box. Keeping all our production and shipping data synchronized ensures our customers avoid delays—especially important for research projects tied to grant or project deadlines.
As product applications expand, unique challenges arise. Some clients have tried to adapt this compound for materials chemistry, reporting issues around batch photostability. Rather than leaving this as an external issue, we engaged our analytic chemists and modified our lamp exposure testing. Fresh strategies in stabilizer package selection came out of that initiative, feeding solutions back to both internal projects and external partners. When feedback pointed to downstream hydrolysis under aggressive scale-up, we brought in engineering chemists to test alternative neutralization agents and pressure-filtration gear. These process “tweaks” keep clients advancing instead of getting stuck at problem points missed in early R&D.
Every production run, every feedback cycle, feeds a continuous improvement model. Team members keep logbooks full of both successful improvisations and failed tests, and we circulate those case studies during quarterly training. Our partners benefit through improved responsiveness—not just in documented process changes, but in the steady march toward more reliable, greener, and safer products.
The technical journey behind 2-Pyridinemethanamine, 3-bromo-α-[(3,5-difluorophenyl)methyl]-6-[3-methyl-3-(methylsulfonyl)-1-butyn-1-yl]-, (αS)- is more than a matter of molecular substitution or cataloging. Each run connects to actual people—chemists chasing milestones, research leaders balancing deadlines, and operators working through difficult process conditions. The commitments we’ve built into our manufacturing process reflect what we've learned from being on both sides of the bench: that reliable and transparent production isn't just nice to have; it forms an unspoken contract with every experimenter relying on our chemicals.
Focusing on continuous improvement, close technical communication, and direct support, we maintain a clear standard. At every stage—from raw material intake through process journals and all the way to cold-packed shipment—every detail speaks to our ongoing investment in reliability and collaborative progress. Our compound stands apart not because of a flashy marketing campaign, but because of lessons earned and partnerships built over years of challenge, iteration, and mutual respect.