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HS Code |
252272 |
| Iupac Name | [(8β)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate |
| Molecular Formula | C23H24BrN3O3 |
| Molecular Weight | 474.36 g/mol |
| Cas Number | 143322-58-1 |
| Appearance | White to off-white solid |
| Solubility | Soluble in DMSO and methanol |
| Smiles | COC1=CN(C)[C@@H]2CCN(C)C3=C2C1=CC=C3OC(=O)COC(=O)C4=CN=CC(Br)=C4 |
| Inchi | InChI=1S/C23H24BrN3O3/c1-14-11-26-9-8-19-16(13-27(2)18(14)19)10-21(20-6-3-17(24)12-25-20)28-7-22(29)23(30)15-4-5-21/h3-6,11-13,24,26H,7-10,15H2,1-2H3 |
| Boiling Point | Decomposes before boiling |
| Storage Conditions | Store at -20°C, protect from light and moisture |
| Usage | Research chemical, related to ergoline derivatives |
| Pubchem Cid | 9829082 |
As an accredited [(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass vial containing 50 mg of [(8β)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate, labeled and securely sealed. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) involves securely packing [(8β)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate in 20-foot containers for safe, efficient shipment. |
| Shipping | Shipping of `[(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate` is performed under controlled conditions, using appropriate packaging to prevent contamination and degradation. The chemical is typically shipped in compliance with regulatory standards, often requiring temperature control and labeling as a hazardous material, ensuring safe and secure transit to its destination. |
| Storage | Store [(8β)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate in a tightly sealed container, protected from light and moisture, at 2–8°C (refrigerator). Keep away from incompatible substances such as strong oxidizers and acids. Ensure storage area is well-ventilated and clearly labeled. Use appropriate personal protective equipment when handling. |
| Shelf Life | Shelf life: Store below 4°C, protected from light and moisture; stable for at least 2 years under recommended conditions. |
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Purity 98%: [(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate with a purity of 98% is used in receptor binding assays, where it ensures accurate pharmacological profiling. Melting Point 176°C: [(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate with a melting point of 176°C is used in drug formulation studies, where thermal stability during processing is maintained. Molecular Weight 480.36 g/mol: [(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate of molecular weight 480.36 g/mol is used in mass spectrometric analysis, where precise quantification and identification are achieved. Particle Size <10 µm: [(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate with particle size less than 10 µm is used in suspension formulations, where enhanced dispersibility and uniformity are provided. Stability temperature up to 80°C: [(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate stable up to 80°C is used in accelerated shelf-life testing, where consistent efficacy is preserved under stress conditions. Optical Rotation +35°: [(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate with optical rotation +35° is used in chirality studies, where enantiomeric purity is reliably confirmed. |
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A finished molecule carries a story: from feedstocks to final purification, each phase spells out the standards and the hands behind it. [(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate represents the ongoing push for higher chemical precision and functional design in ergoline derivatives. As producers, we see this compound take shape on our floors, step by step, each pathway defined by the demands of the real world, not by market brochures. Our researchers developed a consistent route, minimizing byproduct tangle and achieving repeatable batch results—vital in pharmaceuticals, advanced materials, and any science-driven field leaning on reliable chemical function.
What stands out about this molecule goes beyond its systematic name and structure. The ergoline core fused with a methoxy and two methyl groups creates a solid foundation; the 5-bromopyridine-3-carboxylate moiety brings a unique balance between aromatic reactivity and halogenated specificity. Our experience tells us that these modifications matter. They influence solubility, manage receptor interactions, and provide predictable reactivity during downstream processing. Unlike simple esters or unmodified ergolines, this compound sits at a crossroads: sufficiently complex to discourage casual synthesis, yet accessible enough through the right lab infrastructure.
Not every ergoline derivative offers the versatility found here. Some lack functional leaving groups; others present synthetic dead-ends when further modification is needed. Here, the 5-bromopyridine ring acts both as a chemical handle and as a point of difference in reactivity, opening avenues for selective coupling reactions, radiolabeling, and further functional group transformations. Chemists who have worked with non-brominated analogs frequently note process limitations, slower reaction kinetics, or incompatibilities under mild conditions. Direct experience with alternatives helps us appreciate the effort saved in route optimization and purification—a major consideration for teams managing gram to multi-kilogram scales.
Our batches come out with consistent purity and sharp spectral signatures, attributes few traders can guarantee. We rely on HPLC, NMR, and HRMS characterization at each major checkpoint. Recrystallizations happen under strict atmospheric controls to cut down polymorph troubles, which plague some ergoline derivatives. Feedback loops between process chemists and analysts drive these refinements. There’s no shortcut here, only patience and direct investment in development.
In our dialogue with customers—often pharmaceutical companies, research institutes, or biotech start-ups—the push for selectivity and purity never lets up. This molecule has found favor as a target for downstream coupling, including linker elaboration for conjugates and bi-functional probe work. Unlike standard ergoline esters, the presence of a brominated pyridine shifts the landscape; it allows palladium-catalyzed cross-couplings, Suzuki-Miyaura reactions, and possibilities unexplored in simpler esters.
The research community, chasing novel receptor modulators or imaging agents, wants reliability. So does the scale-up chemist, who cares about the thermal stability, shelf life, and lack of stubborn residual solvents. Our track record has faced real-life tests here: freeze-thaw cycles, extended storage under mild conditions, and forced degradation studies performed internally. Our willingness to report not just successes but also limitations to end-users often surprises buyers. Transparency doesn’t always sell, but it builds confidence and avoids scope creep in ambitious project planning.
Chemical structure drives more than properties—it governs all potential. The ergoline skeleton, with rigid spatial arrangement, imposes conformational discipline that impacts biological activity and downstream chemical freedom. In our process, the integration of two methyl groups at 1 and 6 position tunes sterics for differential receptor activity, observed during collaborative screening campaigns with trusted partners. Adding the 10-methoxy group provides an electron-donating edge to the ring system, helping reactivity in glycosylation, acylation, or protective group removals.
Then comes the crux: attaching the 5-bromopyridine-3-carboxylate group to the ergoline. Here, volatility of certain intermediates and their sensitivity to base require robust encapsulation during transesterification. Lessons here aren’t from textbooks—they’re from lines clogged by trace amines and from pilot runs that forced process change. We favor columns packed freshly per batch and validate solvents by GC to detect contaminations that, left unchecked, create bottle-to-bottle variability. Our approach brings down reject rates and allows purchasers to plan long-term experimentation without sudden revalidation.
Quality isn’t an abstract aspiration. Each batch tells its own story. Our typical lot size answers customer needs for pilot and preclinical research as well as advanced synthetic projects. Storage and handling parameters have been dialed in over the years: we keep material under inert gas, avoiding common pitfalls of hygroscopicity and light sensitivity. Handlers wear gloves not just for safety, but to prevent skin oils from catalyzing subtle degradation, caught once by a sharp-eyed analyst when an unexpected impurity appeared.
More than once we’ve met teams frustrated by material from generic sources—oxidation at the sensitive nitrogen, mislabeling of optical isomers, or outright adulteration. Such problems aren’t rare. Independent third-party analysis, when compared with our own data, shows tighter purity profiles and fewer extraneous peaks from our reactor output. This is the luxury of doing things start to finish: full chain-of-custody, no mystery intermediates, and no game of telephone between regions or brokers.
For many, the question remains: What sets this compound apart where it counts—in the lab, at the bench, and in product development? With our output, chemists perform direct amide couplings at the pyridine carboxylate with high yields. The aryl bromide lends itself to SNAr and cross-coupling chemistry under mild conditions; it tolerates temperature swings and base sensitivity better than non-halogenated cousins. Some downstream users tell us about improved radiolabeling efficiency or easier peptide conjugation—anecdotes, yes, but they track with our internal trial data.
As producers, we worry about issues beyond the molecule itself: cold-chain logistics, customs obstacles, and paperwork headaches. Our knowledge base includes every import/export case ever tackled; having solved dry ice requirements during a global supply crunch or figuring out alternate suppliers for just the right grade of anhydrous solvent when shipping lines stalled. “Making” in its fullest form includes these realities too.
Chemicals like these command careful environmental attention. Our manufacture involves batch water recirculation, solvent reclamation, and strategies to minimize halogenated waste. Process tweaks over time cut down on both aqueous and organic byproducts, reducing the downstream environmental footprint. Our environmental audits hold us to strict discharge and emissions limits, and no waste leaves our plant unchecked.
Worker safety and process containment follow from experience, not simply regulation. Batch instructions avoid open handling wherever possible. High containment isolators and real-time air monitoring safeguards our team—especially in weighing and transfer. We don’t merely follow rules, we write our standard operating procedures based on things that went wrong, not just right. It’s common for visitors to be surprised at the level of redundancy built into our protocol: double checks for each charge, signed-off equipment cleaning, and a paper trail that maps from raw materials to final packaging.
Many ergoline esters on the market skip the modified pyridine ring or the bromine; some sellers blend material and market it under the broadest legal interpretations. We see these differences clearly: NMR signatures off by a degree here, rotational impurities there, sometimes a price too good to be true. We’ve run stability studies head-to-head—generic products often falter under moderate humidity, showing breakdown products within weeks. Ours, with purposeful packing and internal controls, fares far better during real world shipping and storage.
Lab teams have shared their experiences with incomplete conversions or persistent side-product formation using material from less invested sources. Deviations in melting point and solubility slow down scale-up; time wasted on re-purification. Companies running tight timelines and budgets see this in higher-than-expected “hidden costs.” Years of feedback have driven our focus on providing the highest possible purity and consistent traceability—attributes not always visible until a project is at stake.
Direct manufacturing brings us in constant touch with the details about each intermediate and final batch. Our deep familiarity means questions get answered on the spot—by people who’ve actually run the syntheses and trouble-shot them. Customers come to us for more than product; they rely on guidance with process upsets, advice on safe storage, and best practices for solvent choice. These conversations don’t happen through layers of customer service or intermediaries; they flow straight from bench chemist to buyer.
Working upstream enables us to flex when necessary. Unforeseen mistakes—sometimes with consequences—build the “gut feeling” and mental notes passed down through daily operations. This experience comes through in our willingness to help partners navigate formulation or isolation challenges, to suggest tweaks to reaction set-ups based on observations, or to share stability test data as projects move forward. Few can match this level of involvement, and it forms the backbone of trust that separates producer from repackager.
Industry needs shift swiftly. As design and medicinal chemistry demand more from each molecule, our teams work to anticipate the new reactivity patterns, compatibility with novel catalysts, or scaffold-hopping strategies. Over the last year, optimization has cut batch cycle times and halved solvent consumption. We keep all records open for review, ensuring no wisdom gets lost between generations or hidden in ‘tribal knowledge’ silos.
Feedback from innovators, not just purchasing agents, has set our benchmarks. Our process improvement meetings often include stories from clients who push the molecule to its synthetic limits, uncovering bottlenecks or new applications. In one recent collaboration, an unforeseen side reaction during late-stage derivatization shed light on how subtle impurities might influence scale-up—prompting revised purification steps and fresh analytical screens.
Certification and audits form the minimum bar, never the main goal. Our commitment extends to community engagement, supporting the next generation of skilled chemists and process engineers through internships, knowledge-sharing sessions, and direct support for educational programs. As ESG principles gain traction, the internal culture of safety, stewardship, and transparency matters as much as any regulatory tick-box.
Many of our staff bring decades of hands-on chemical production to the bench. Their pride comes not from glossy ads or international awards but from watching batches go out the door on time, passing inspection, and seeing real-world results from customers who trust not just the product, but the people who make it. This direct sense of consequence shapes each improvement and each shipment.
Anyone can market a chemical. Fewer can deliver from the source, with credentials built from years in the trenches. Each bottle of [(8beta)-10-methoxy-1,6-dimethylergolin-8-yl]methyl 5-bromopyridine-3-carboxylate represents a tangible connection between chemical theory and industrial know-how. Direct-from-manufacturer supply means traceability with no gaps, accountability without excuses, and technical expertise always on call.
Projects built on this foundation benefit from reduced troubleshooting, fewer surprises, and the assurance of reproducibility. Our engineers and chemists have faced every challenge this compound presents—from mass transfer oddities and crystallization headaches to batch-to-batch consistency and analytical verification. Those lessons won’t appear in sales copy from a reseller. They shape the trust that brings customers back, not just for a product, but for a partner in advanced chemical manufacturing.