|
HS Code |
449458 |
| Product Name | Methyl 6-Bromonicotinate |
| Cas Number | 20559-55-1 |
| Molecular Formula | C7H6BrNO2 |
| Molecular Weight | 216.03 g/mol |
| Appearance | White to off-white solid |
| Purity | Typically ≥98% |
| Melting Point | 70-74°C |
| Solubility | Soluble in organic solvents such as ethanol, DMSO, and methanol |
| Smiles | COC(=O)c1ccc(Br)nc1 |
| Inchi | InChI=1S/C7H6BrNO2/c1-11-7(10)5-2-3-6(8)9-4-5/h2-4H,1H3 |
As an accredited Methyl 6-Bromonicotinate factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Methyl 6-Bromonicotinate, 5g: Supplied in an amber glass bottle with a secure screw cap, labeled with product details and safety information. |
| Shipping | Methyl 6-Bromonicotinate is shipped in tightly sealed containers to prevent moisture and contamination. It is packed in accordance with regulations for handling hazardous chemicals, often classified under UN hazard classes. Proper labeling and accompanying safety documentation are provided. The product is transported at ambient temperature, away from incompatible substances. |
| Storage | Methyl 6-Bromonicotinate should be stored in a tightly sealed container under cool, dry, and well-ventilated conditions, away from direct sunlight and sources of heat or ignition. Keep it separated from incompatible substances such as strong oxidizers. Store at room temperature or as recommended on the safety data sheet (SDS). Ensure appropriate labeling and access for trained personnel only. |
Applications of Methyl 6-Bromonicotinate in Industrial ManufacturingMethyl 6-Bromonicotinate is a specialized chemical intermediate synthesized in our facilities for advanced sectors. Our production is tightly aligned with the strict parameters, formulation needs, and downstream integration requirements of regulated manufacturing domains. Below, we detail core real-world industrial segments making routine use of this intermediate across value-added processes. 1. Active Pharmaceutical Ingredient Synthesis – Pyridine-Based Drug IntermediatesPharmaceutical manufacturers employ this intermediate for constructing pyridine ring systems in complex drug APIs, notably in the cardiovascular and central nervous system categories. The structure’s bromine functional group supports targeted substitution reactions under controlled conditions, reducing side reactions and improving batch reproducibility. Plant chemists precisely adjust the feed ratio depending on reaction scale, catalyst system, and regulatory submission requirements, targeting minimal residual impurity levels. Customer audits focus on traceability, impurity profiles, and reagent origins before integrating this intermediate into GMP-validated API synthesis lines. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
2. Crop Protection – Synthesis of Agrochemical ActivesAgrochemical companies use this intermediate to manufacture pyridine-derived pesticides, herbicides, and insecticides. The compound delivers controlled reactivity, enabling selective halogenation steps necessary for building bioactive skeletons. During technical-grade pesticide production, our end users rely on clean, spectrum-confirmed batches to minimize downstream waste and support regulatory dossier submissions. Product application teams typically modify ratios based on pesticide specificity and seasonal campaign volumes. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
3. Specialty Materials – Fluorophore and Dye SynthesisSpecialty chemical manufacturers value this compound as a building block in the controlled synthesis of advanced fluorescent dyes and markers, widely applied in biological imaging and analytical chemistry. By leveraging the bromine-activated pyridine core, downstream labs perform regioselective substitutions to fine-tune optical properties while tightly monitoring the purity and residual halogen content of intermediates. Our batches support high-purity requirements and low residual solvent tolerances to fit the precision needs of the specialty materials segment. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
4. Chemical Research Reagents – Fine Chemical and Catalyst DevelopmentChemical and pharmaceutical R&D labs regularly procure this intermediate as a reliable substrate for exploratory synthesis, catalyst discovery, and method validation exercises. The compound’s distinctive bromo-pyridine configuration makes it a favored reference molecule in structure–activity studies and innovative ligand frameworks. Research chemists systematically evaluate batch properties and documentation (full CoA, NMR/HPLC spectra) for reproducibility in new bench-scale reactions, patent work, and publication-grade projects. Industry compliance standards
Typical usage ratio
Downstream process integration
Final product types
|
Competitive Methyl 6-Bromonicotinate prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please call us at +8615371019725 or mail to admin@sinochem-nanjing.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: admin@sinochem-nanjing.com
Flexible payment, competitive price, premium service - Inquire now!
In our chemical plants, the distinct scent and character of methyl 6-bromonicotinate have become familiar. Many years have passed since we made the decision to perfect the production of this specialized nicotinate derivative, and that experience influences every drum that leaves our gate. This molecule, recognized by its brominated pyridine ring, stands apart from standard methyl nicotinates and other halogenated variants. The selective placement of the bromine atom at the 6-position brings unique reactivity and remains indispensable for chemists in search of building blocks that sidestep unwanted side reactions.
Our material, produced at scale with a continuous process we have tested and refined many cycles over, respects tight purity thresholds. Each batch offers a consistent white to off-white crystalline appearance, minimal residual solvents, and a reliable assay above 98 percent. We do not consider matching a certificate of analysis as the only job. Operators check and recheck for off-odors and color impurities, and our chemists fine-tune crystallization and drying conditions to keep oxidative degradation low. Variations in ambient humidity, fluctuations in incoming raw materials, and small changes in reaction heat loads all push us to remain vigilant, since every factor has taught us that process controls make or break this product’s quality.
The formal CAS registry number is a common starting point: 5470-70-2. Still, we know from experience that not every sample from every source performs the same in practice. The methyl ester gives it a volatility and solubility uncommon among many pyridine derivatives. During the filtration and washing stages, care must guarantee tight particle size that does not slow final use downstream. From UV trace analyses to the fine control of moisture content (usually below 0.50 percent), each data point counts. These might look technical, but our flask-to-drum tests confirm what our customers soon notice: a product that dissolves quickly, weighs out as expected, and holds potency from first synthesis to the last granule of the job.
Methyl 6-bromonicotinate serves as a core intermediate for pharmaceuticals, crop protection chemicals, and specialty materials. Our early conversations with process development teams taught us that not just any substituted nicotinate will behave as needed. Without 6-bromo selectivity, synthetic routes stall or fill up with unwanted isomers. Years before automated workflows, our operators learned to spot color changes or nitrogenous odors that might signal a missed endpoint or contamination from other halopyridines. That attention keeps today's streams pure and focused on the 6-bromo regioisomer, which downstream manufacturers rely upon.
In-house trials and customer feedback confirm the value of methyl 6-bromonicotinate in Suzuki-Miyaura and other palladium-catalyzed couplings. Its bromine atom, strong enough for clean reactivity yet not so stubborn as to yield low conversions, hits the sweet spot for C–C, C–N, or even C–O bond-forming steps. The methyl ester opens paths to saponification or amidation without fuss, sidestepping the slow kinetics of bulkier or ethyl counterparts. When we spent time optimizing for laboratory through to multi-kilogram campaigns, common pitfalls appeared—batch-to-batch variability, slow crystallizations, poor filtration. By tightening agitation rates and using proprietary filtration media, our teams shaved hours off cycle times.
Comparison tables come up often—methyl 2-bromonicotinate, ethyl 6-bromonicotinate, plain nicotinic acid, and unhalogenated esters cycle through industry discussions. Yet side-by-side, key distinctions keep methyl 6-bromonicotinate as the favored option once manufacturing goals are declared. The reactivity of the 6-bromo position balances stability during storage and shipping, hampering premature debromination. We tested ethyl 6-bromonicotinate for some time, since its higher boiling point can fit other processing windows, but quickly discovered tradeoffs in solubility profiles and handling in cold weather.
The methyl group, smaller than ethyl or butyl, imparts not only slight lowering of melting points (consistent around 65-67 Celsius) but also easier saponification. It shortens cycle times during ester cleavage and speeds up preparation of downstream amides, acids, or even nitriles. Whether in liquid or solid-phase synthesis routes, the difference for the bench chemist or kilo pilot team appears in both yield and overall speed. From the plant floor, handling methyl 6-bromonicotinate introduces fewer dusting or clumping issues than its more hydrophobic cousins. We make sure the bulk flows evenly and seals tight against ambient moisture—a lesson learned after a few cases of bridged material in earlier years.
Every kilogram we refill contributes to new batch records in pharma-focused and agrochemical labs. The typical user values not having to filter out dimeric pyridines or overbrominated byproducts. Inclusion of bromine in the 6-position—rather than on carbons two or four—maintains cleaner conversion in multi-step sequences and less risk of halogen-labile side chains reacting upstream. Our quality assurance teams monitor retention times and IR spectra with the same care as cleanroom standards, having seen the downstream trouble that even small isomeric impurities can create. Drug substance manufacturers especially highlight this difference when troubleshooting yield losses or erratic reactions with third-party material.
From the start, we noticed that methyl 6-bromonicotinate required tweaks in storage recommendations. It holds its character best in tightly sealed, inert-lined vessels. Open bags in humid months and the product will cake or yellow, which our old records show can accelerate even in short spells. To head off these issues, crews now load all bulk shipments into heavy-wall HDPE or lined fiber drums under low-humidity environments; we fill smaller lots by weight, using desiccants for added insurance. Sensitive to both excess heat and high pH, the material fares best in cool, dark warehouses, and we label every pack with date of fill and recommended storage temperatures.
Transporting it means careful route selection—shorter travel times reduce gradual loss of potency, especially in warm climates. Our logistics group scanned years of shipping data and responded by adjusting insulation and pallet stretch wrap in hotter seasons. The goal is the same: finished goods arrive at the same purity and handling condition across the shipment, whether bound for a local kilo lab or a multinational formulation site.
In new chemical entity research, methyl 6-bromonicotinate grants process chemists leeway to introduce a bromine tag at one of the less reactive pyridine carbons. Compared with non-halogenated nicotinates, the bromine allows for routes to fluorinated, aminated, or alkylated analogs using modern palladium or copper cross-coupling reactions. Many projects in heterocyclic API synthesis started with the basics: set up the bromine, build out the core, then remove or replace that handle as the molecule grows.
On the agrochemicals side, the brominated aromatic ring assists in tuning activity or environmental mobility in new herbicidal or fungicidal compounds, often by affording selective refunctionalization through metal-catalyzed chemistry. Years of close cooperation with R&D users taught us that inconsistent batches or minor impurities unwind whole suites of downstream data. As a result, we back up every fresh lot with full traceability and offer supporting impurity profiles alongside the material.
Moving from bench top to several-ton campaigns rarely happens without headaches. Early trial runs produced more off-cuts than saleable product. Over the years, solution lay in never locking ourselves into fixed thinking—adjusting ratios and controlling reagent addition rates created much tidier product and less waste. One memorable round of troubleshooting involved odd black particulates seen in only two of our largest dryers; root cause traced to a slight drift in vacuum level leading to thermal degradation. Correcting that taught us the value of adjoining stable engineering controls with hands-on daily monitoring.
Pushing yield and keeping waste low make a difference over many cycles. Modest improvements—in tightening the control of starting material purity, shifting cooling curve protocols, or upgrading to finer filtration—save costs and improve environmental footprint over hundreds of tons shipped. When small product losses end up on packaging lines, whole campaigns run over-budget. The more we invested in operator training, refining batch documentation, and simple process FMEAs, the lower our annual deviation rates. Some of these changes may not be visible outside our walls, but over time, end users see the impact directly in batch consistency and storability.
Safety never stays static in a working plant. Handling strong bromine donors and pyridine derivatives taught us respect for both acute reactivity and longer-term exposure profiles. Regular air monitoring, review of MSDS guidelines, and respirator fit tests make up routine checks before loading or transferring methyl 6-bromonicotinate. From past issues, we learned to nip static accumulation and accidental exposure scenarios before they escalate. Spill containment, prompt neutralization, and detailed operator drills keep our workplace as safe as possible. Regular lessons drawn from close calls or new regulatory reviews become procedure as quickly as they are recognized.
We also heard the message growing louder each year to support cleaner chemistry. Focus switched to solvent recovery, controlled venting, and energy reduction in distillation. As waste management regulations sharpened, our older incineration practice gave way to closed-loop and licensed offsite handling, making every production step safer and more responsible. Not every customer sees this infrastructure, but it lines up with their own compliance demands. Our in-house personnel developed waste minimization benchmarks—not only for methyl 6-bromonicotinate but across similar halopyridines—which we share with partners seeking to green up their flows as well.
Years in chemical manufacturing set the realities apart from promotional spin. Few molecules teach quite the same combination of chemistry, safety, and process control as methyl 6-bromonicotinate. On the ground, every kilogram passing QA means more than a product order—it reflects hundreds of small adjustments, equipment upgrades, and bench-to-plant translations that keep the supply line moving. Lessons learned from off-spec experiences, unexpected customer needs, and supply chain snarls feed back into next year’s process revisions. No off-the-shelf procedure or single spec sheet carries that kind of background.
Requests still arrive for custom packaging, alternative solvents, or specialized purity levels. Some projects need lowest possible particle size, others seek minimized residual solvents for stricter ICH applications. Each demand circles back to our collaborative approach; we offer evidence of what does or doesn’t work, never shy about sharing pitfalls visible only after years on the job. The dialogue between producer and user sharpens over time, and improvements stack up in real-world results.
What keeps us working at each new batch isn’t a simple pursuit of volume. Quality, delivery, and adaptation to shifting regulatory standards all form core objectives. New demands, like green chemistry mandates or micro-contamination tracking, push processes further. Regular customer audits, surprise regulatory inspections, and even feedback from handlers reshaping the field packaging inform upcoming investments—whether in people, plant, or analytical tech.
In coming years, tighter environmental controls, stricter documentation, and deeper analytical expectations will raise the bar again. Meeting these shifts doesn’t start from a blank slate. Ongoing dialogue with production staff, on-site chemists, and end-user technical leads continues guiding change. From raw bromine handling, through niche pyridine coupling, to the final filled and tested drum, every touchpoint shapes what methyl 6-bromonicotinate stands for in practice—not just as a line in a catalog, but as a compound carrying the weight of years’ expertise.
The evolution of this building block remains a shared story between manufacturer and user. Real results show up not in brochures but in production turnovers, analytical records, and successful downstream syntheses. Standing behind each lot, we remember what went into earning that reliability—batch by batch, day after day.