|
HS Code |
790878 |
| Chemical Name | 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester |
| Cas Number | 199775-14-7 |
| Molecular Formula | C7H5BrClNO2 |
| Molecular Weight | 250.48 |
| Appearance | Solid |
| Purity | Typically >98% |
| Solubility | Soluble in common organic solvents |
| Smiles | COC(=O)c1cncc(Br)c1Cl |
| Inchi | InChI=1S/C7H5BrClNO2/c1-12-7(11)4-2-3-5(8)6(9)10-4/h2-3H,1H3 |
| Storage Conditions | Store at room temperature, dry and well-sealed |
| Hazard Classification | May cause skin, eye, and respiratory irritation |
| Synonyms | Methyl 5-bromo-2-chloroisonicotinate |
| Usage | Pharmaceutical intermediate |
As an accredited 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 25 grams of 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester, with secure screw cap. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Typically loads 12–14 MT of 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester packed in 25 kg drums. |
| Shipping | The chemical 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester is shipped in tightly sealed containers compliant with chemical safety regulations. It is protected from moisture, heat, and direct sunlight, and labeled according to hazard requirements. Shipping typically uses ground or air transport with appropriate documentation for safe handling and delivery. |
| Storage | Store 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester in a tightly sealed container, in a cool, dry, and well-ventilated place, away from moisture, direct sunlight, and sources of ignition. Keep away from incompatible substances such as strong oxidizing agents. Ensure proper labeling, and access only by trained personnel. Handle in accordance with standard laboratory chemical safety protocols. |
| Shelf Life | Shelf life: Store 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester tightly sealed, protected from light and moisture; stable for 2 years. |
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Purity 98%: 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester with purity 98% is used in pharmaceutical intermediates synthesis, where high purity ensures efficient reaction yield. Molecular weight 264.48 g/mol: 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester with molecular weight 264.48 g/mol is used in medicinal chemistry research, where accurate molecular weight enables precise formulation. Melting point 67-69°C: 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester with melting point 67-69°C is used in solid-state formulation studies, where defined melting behavior aids in process optimization. Particle size <50 µm: 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester with particle size less than 50 µm is used in fine chemical manufacturing, where small particle size enhances dissolution rate. Stability temperature up to 120°C: 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester with stability up to 120°C is used in temperature-controlled reactions, where thermal stability prevents decomposition. Solubility in methanol 25 mg/mL: 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester with solubility in methanol 25 mg/mL is used in analytical method development, where high solubility facilitates sample preparation. HPLC assay ≥99%: 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester with HPLC assay of at least 99% is used in quality control laboratories, where high assay values support product standardization. |
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From the vantage point of a manufacturer who has worked with diverse pyridines for years, certain molecules carve a reputation for themselves based on reactivity, yield, and the type of complexity they unlock for downstream synthesis. 4-Pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester stands out in this category. This compound, recognized in some labs by its shorthand 5-bromo-2-chloro nicotinic acid methyl ester, delivers distinct properties for custom synthetic projects. The combination of bromo and chloro substituents on the pyridine ring is a gateway to subsequent modifications; it provides functional handles for further chemistry—cross-coupling, nucleophilic substitution, and other transformations essential in medicinal, agrochemical, and material science explorations.
We batch every kilogram of this compound from raw material through to finished ester in our ISO-certified facilities. Precise reaction conditions, strict temperature control, and real-time analytics come into play to achieve consistently high purity, typically reaching over 98% (GC/HPLC). This is not a standard methyl pyridine ester with a generic profile—it presents unique synthetic opportunities. The bromine at the 5-position and chlorine at the 2-position set up a distinct regioselective environment that many generic methyl nicotinates or simple pyridine derivatives cannot offer.
There is nothing off-the-shelf about these substituted pyridines. Unlike basic methyl nicotinate, they unlock selective reactivity. As a manufacturer, we have invested in equipment that can handle corrosive reagents and ensure containment during halogenations. This attention to handling both safety and product integrity is based on years of hard lessons and validation runs. Laboratories and companies seeking highly functionalized aromatic intermediates depend on this consistency, whether they run ten-gram discovery batches or multi-tens of kilograms for clinical or pilot production.
Over years of running halogenation and esterification, we have found that the route selected determines more than just price—it impacts the impurity profile, by-product distribution, and subsequent processability. For the 5-bromo-2-chloro methyl ester, direct halogenation on pyridinecarboxylate scaffolds invites side reactions. Instead, we commonly start from suitably substituted pyridines, then build in the ester later, monitoring every synthetic step.
Batch-to-batch variability remains a key concern in pyridine chemistry, especially in complex substituted cases. Side reactions at the 2-position can lead to unwanted dehalogenation or over-substitution, which in downstream uses translates to purification headaches and yield loss. Automated chromatography is not always practical at scale, so designing for high selectivity from the start pays dividends. By running reactions under inert atmosphere and using in-line HPLC, we have minimized batch deviation, saving clients both time and capital in their campaigns.
Anyone searching for a starting point in heterocyclic synthesis or coupling partners for pharmaceutical building blocks quickly learns the limits of simple methyl nicotinates. The 5-bromo, 2-chloro product plugs directly into Suzuki or Buchwald-Hartwig couplings. Medicinal chemists rely on this product to build libraries of candidate compounds with minimal synthetic overhead. The dual halogenated moiety accelerates lead generation by enabling regioselective functionalization—something that can’t be easily achieved using less-functionalized intermediates.
In the agrochemical sector, crop protection research often looks for high-affinity binding scaffolds; here, symmetrical substitution does not offer the molecular recognition or binding specificity that unique substitution patterns provide. This methyl ester, bearing specific halogens, gives a platform for quick analog generation, enabling discovery teams to scan SARs efficiently without back-and-forth route redesign. Material scientists, while a smaller segment, use these compounds to tune electronic or photophysical behaviors when building organic electronic materials or ligands.
The uniqueness of 4-pyridinecarboxylic acid, 5-bromo-2-chloro-, methyl ester lies in its dual-halogen architecture. Most competitors offer mono-halogenated or non-halogenated pyridines. In day-to-day synthesis, every additional reactive site simplifies route design for our clients. Mono-halogenated analogs rarely give the orthogonal chemistry this product enables. For example, substitution can occur selectively at the 5-bromo or 2-chloro; this dramatically widens the variety of accessible derivatives.
From our experience, unmatched selectivity in coupling means fewer protection-deprotection steps down the line. That saves real money for pharmaceutical clients, both in raw material savings and compliance, since fewer reagents and solvents are consumed and disposed of. Many multi-step synthetic routes can be collapsed into fewer operations if the right starting material, such as our methyl ester, is chosen.
Shelf stability and storage, often glossed over, become crucial at scale. Some methyl nicotinates with sensitive functional groups degrade under even mild humidity or temperature variation. By controlling residual solvents and packaging in inert gas, we provide material that can sit reliably in inventory for months without loss of activity—a key requirement when clients schedule production campaigns.
Every lot carries full analytical documentation, including NMR, HPLC, GC, and where relevant, mass spectrometry confirmation. Decades of technical troubleshooting have taught us that transparency pays back in reduced technical service requests. We keep detailed records tracking back to each starting material lot and personnel responsible for each batch. In the rare case that something fails to meet spec—a reaction deviation, an out-of-range impurity—the material never leaves our gates. Clients get what we use ourselves in downstream chemistry.
Our long-term partners regularly request custom impurity profiles, tailored particle size, or even isotopically labeled material. Having our own facility and a decade-spanning team, we scale these adaptations without passing through intermediaries or juggling multiple paperwork layers. The result is direct dialogue and solutions grounded in real synthetic experience.
Hazard management starts with the right information on hand. Personnel can’t afford surprises with halogenated pyridines, which can be skin and eye irritants. Our product packages come with thorough documentation and handling recommendations. Training operators in correct PPE and procedures takes time, but the payoff is zero reportable incidents over years of operation. We keep emergency spill supplies in dedicated zones and ensure all staff undergo regular upskilling in chemical management.
Packaging has evolved too. Early runs relied on basic HDPE bottles or drums, but failures in transit taught valuable lessons. We switched to fluorinated containers and reinforced outer packaging for export. Care in sealing and inerting every shipment minimizes any risk from moisture ingress or temperature excursions.
Years of support for pharmaceutical partners shape our perspective. Often, the difference between a successful campaign and one stuck in purification arises from the right intermediate. Medicinal chemists use this methyl ester in heterocyclic ring expansions, cross-coupling, and amide bond formation. Each transformation amplifies the value locked in by the unique halogenation pattern, which cannot be easily replicated by modifying cheaper precursors.
Clients return for scaled batches because we adapt specifications over time—one company recently requested a lot with minimized 3-halogen impurity, which we delivered by optimizing reagent equivalents and refining our purification. Others operate under GMP regulations, so our approach extends to supplying batch-level documentation and following validated cleaning procedures for dedicated lines.
In academic settings, the ester group presents opportunities for selective hydrolysis or transesterification experiments, tracking conversion rates and mechanistic pathways for publication. Even outside pharmaceutical and academic use, in pigment and materials science, this compound gets incorporated into more advanced frameworks, benefiting from enhanced electron-withdrawing properties thanks to the halogens.
COVID-19 and disruptions in global logistics highlighted vulnerabilities in relying solely on outside traders or third-party producers. Our direct control of sourcing, warehousing, and shipping means partners avoid last-minute panic. As the original producer, we adjust batch sizes in real time and maintain buffer stock of key halogenated building blocks.
Mutual trust means sharing forecasts and pipeline signals. We keep surplus capacity during high-demand periods and regularly update our synthetic pathways based on regulatory requirements or changing client needs. Our senior chemists meet monthly not just with marketing, but with client-facing technical teams, to catch issues early and innovate new solutions, such as greener reagents or recycle streams for spent halides.
Price stability comes from decades working with the same upstream raw material suppliers. By owning the risk—and the reward—of sourcing, we offer long-term contracts and volume discounts that traders can’t match, cutting out delays and reprocessing costs. This lets our partners plan resource allocation with confidence, knowing that the product specifications and logistics stay the same from batch to batch.
As synthetic chemists and operators, we see every waste stream and solvent barrel at the plant. Efforts to improve sustainability start on the floor, not the balance sheet. We launched solvent recycling initiatives for every step in the 5-bromo-2-chloro methyl ester process, achieving a 30% reduction in fresh solvent use compared to earlier years. By switching energy-intensive steps to continuous flow and improving reactor insulation, we lowered energy consumption and kept emissions within tightening local regulations.
Halogenated intermediates historically drew deserved scrutiny for their persistence and byproduct formation. Our process development group works with NGOs and regulatory agencies to preempt potential issues long before inspections arrive. By disclosing all degradation products, we support customers preparing their own safety dossiers and environmental assessments.
The future will bring new challenges—possible restrictions on certain halogenated products, customer needs for even cleaner starting materials, or the need for greener synthetic routes. We’re piloting enzymatic and photoredox approaches to heterocyclic halogenation, aiming for even greater process efficiency and lower waste. Every improvement gets shared with our long-term clients, who rely on transparency and quality for their own compliance and innovation.
Over the years, we’ve met too many researchers frustrated by inconsistent quality or slow response from distributors. As the actual manufacturer, we understand what happens on a molecular level—and how that translates to reliability in the lab or plant. Each time a client scales from grams to multi-kilo orders, we see in real time what works and what breaks down, so we continue refining both the product and the process to meet real-world demands.
Our commitment extends beyond the substance itself, into relationships built on problem-solving, direct feedback, and innovation grounded in decades of technical experience. Whether in pharma development, agricultural research, or specialty materials synthesis, this methyl ester remains one of the few building blocks crafted by chemists for chemists, shaped by first-hand understanding of the entire supply chain. We believe in openness, honesty, and continuous improvement, driving better chemistry for every step in our partners’ journeys.