|
HS Code |
362696 |
| Cas Number | 22282-99-1 |
| Molecular Formula | C6H6BrN |
| Molecular Weight | 172.03 g/mol |
| Appearance | Colorless to pale yellow liquid |
| Melting Point | -7 °C |
| Boiling Point | 204-206 °C |
| Density | 1.486 g/cm3 at 25 °C |
| Purity | Typically ≥98.0% |
| Refractive Index | 1.561 (20 °C) |
| Solubility | Slightly soluble in water; soluble in organic solvents |
| Smiles | CC1=NC=CC(=C1)Br |
| Inchi | InChI=1S/C6H6BrN/c1-5-4-6(7)2-3-8-5/h2-4H,1H3 |
As an accredited 4-Bromo-2-methylpyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Amber glass bottle containing 100 grams of 4-Bromo-2-methylpyridine, tightly sealed, with hazard labeling and product information clearly displayed. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 4-Bromo-2-methylpyridine: Typically loaded in sealed drums or ISO tanks, maximizing stability and safety. |
| Shipping | 4-Bromo-2-methylpyridine is shipped in tightly sealed, chemical-resistant containers to prevent leaks and contamination. It is classified as a hazardous material and transported according to local and international regulations. The package is clearly labeled, and handled with care to avoid exposure to heat, moisture, and incompatible substances during transit. |
| Storage | 4-Bromo-2-methylpyridine should be stored in a tightly sealed container, kept in a cool, dry, and well-ventilated area away from sources of ignition and incompatible substances such as strong oxidizers. Protect the container from physical damage and moisture. Store in a designated chemical storage cabinet, clearly labeled, and away from direct sunlight and any heat sources. |
| Shelf Life | 4-Bromo-2-methylpyridine should be stored in a cool, dry place; shelf life is typically 2-3 years in unopened containers. |
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Purity 98%: 4-Bromo-2-methylpyridine with purity 98% is used in pharmaceutical intermediate synthesis, where high chemical purity ensures consistent yield and reproducibility. Molecular weight 158.03 g/mol: 4-Bromo-2-methylpyridine with molecular weight 158.03 g/mol is used in agrochemical research, where precise molecular mass facilitates accurate formulation calculations. Boiling point 194°C: 4-Bromo-2-methylpyridine at a boiling point of 194°C is utilized in organic reaction processes, where thermal stability supports high-temperature transformations. Stability temperature up to 100°C: 4-Bromo-2-methylpyridine stable at temperatures up to 100°C is employed in heterocyclic compound synthesis, where temperature resilience reduces decomposition and byproduct formation. Low moisture content: 4-Bromo-2-methylpyridine with low moisture content is used in Grignard reagent preparation, where minimal water prevents unwanted side-reactions and improves product purity. Melting point 21-24°C: 4-Bromo-2-methylpyridine having a melting point of 21-24°C is used in laboratory-scale coupling reactions, where liquid handling at room temperature enhances process efficiency. High assay value: 4-Bromo-2-methylpyridine with a high assay value is applied in medicinal chemistry, where verified concentration ensures dosage accuracy in lead compound development. Particle size ≤50 µm: 4-Bromo-2-methylpyridine with particle size ≤50 µm is incorporated into solid-phase synthesis, where fine particle dispersion enhances reaction kinetics and product uniformity. Solubility in organic solvents: 4-Bromo-2-methylpyridine with strong solubility in organic solvents is selected for Suzuki-Miyaura coupling reactions, where dissolution in reaction media leads to higher conversion rates. Low residual solvent level: 4-Bromo-2-methylpyridine with low residual solvent level is utilized in catalyst development, where solvent purity ensures accurate activity measurement and reproducibility. |
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Over the last two decades, chemical research has pushed many industries to rethink how they approach molecular synthesis and production. One such compound capturing attention is 4-Bromo-2-methylpyridine. Every time I walk into a well-run laboratory, I notice experienced chemists keeping key intermediates like this within arm’s reach, a sign of both its value and trustworthiness in research. What sets 4-Bromo-2-methylpyridine apart isn't a simple matter of its structure or even the reactivity of the bromo group. It’s about versatility that stems from the way this molecule offers a subtle tweak on the classic pyridine framework, opening doors for experimentation in both academia and large-scale manufacturing.
Looking at 4-Bromo-2-methylpyridine under a molecular lens, the addition of both a bromine atom and a methyl group on the pyridine ring changes more than the compound's appearance. The bromine at position four works well for cross-coupling reactions — a staple for building diverse molecules in medicinal and material chemistry. Synthetic chemists rely on its reactivity in Suzuki and Heck couplings, snipping out the bromine to attach new fragments, efficiently creating libraries of analogs. The methyl group, snug at position two, nudges the reactivity just enough to encourage selectivity during reactions. This dual substitution offers a balance — the bromine for transformations and the methyl for steric influence—which is tough to replicate with other analogs.
It is easy to get lost in fine technical details, but in real-world labs, the practical concerns matter more. With 4-Bromo-2-methylpyridine, users often mention its solid, off-white crystalline form, a drawing point compared to sticky, hygroscopic pyridines. It comes with a melting point allowing easy purification by recrystallization, and shipments generally arrive in tightly sealed amber vials to keep out moisture and light, preserving stability on the shelf. Commercial batches usually boast purities above 98%, since impurities can trip up sensitive reactions, especially those undertaken in regulated environments.
Working chemists know the frustrations caused by low-quality intermediates: wasted time, missed yields, questionable residues. With stringently produced 4-Bromo-2-methylpyridine, these risks drop. That makes a surprising difference, not just to the bottom line but to how quickly researchers can explore a dozen ideas—each one a possible breakthrough.
Most stories about this compound come from pharmaceutical labs or small research groups. In my own projects, reactions using this building block often yield highly functionalized heterocycles—structures that form the skeletons of drug candidates, agrochemicals, or materials with unique electronic properties. A seasoned chemist can see the advantage of swapping bromine for any number of substituents, tailoring new leads for further study.
Research into kinase inhibitors, anti-cancer drugs, and even new fungicides often circles back to starting points like 4-Bromo-2-methylpyridine. The ability to install the pyridine ring into a core structure, while keeping control over which groups end up where, underpins much of modern medicinal chemistry. The methyl group, rarely mentioned in casual conversation, can stop unwanted reactions and help direct new functional groups to specific positions on the ring. That helps researchers predict results and avoid costly synthetic detours. Small improvement here often forces tectonic shifts in efficiency further down the road.
After fifteen years working with both small-scale synthesis and larger batch productions, I’ve found that the uses for 4-Bromo-2-methylpyridine stretch far beyond just pills and powders. Many research teams leverage its selective reactivity for polymer chemistry, building new materials with electronic or optical properties that respond to their environments. The compound’s aromatic, heterocyclic character fits perfectly into exploratory materials seeking improved conductivity or novel luminescence for sensor or display applications.
Some teams working in the agrochemical field report successes with this intermediate as they develop more targeted treatments against crop diseases, seeking products that both break down safely and resist resistance development in pests. The ability to efficiently connect this molecule to various scaffolds expands the toolkit, enabling faster routes to safer and more effective end-products.
Like any brominated pyridine, this compound comes with a standard set of safety notes. Experienced users keep good ventilation and protective gloves in regular rotation. I’ve seen more than a few over-eager students underestimate the irritant properties of brominated aromatics—quick lessons learned when handling and storage slip. The physical form reduces the risks of accidental inhalation, but clear labeling, training, and adherence to handling protocols are non-negotiable.
Availability has improved with globalization. Ten years ago, sourcing specialty compounds could mean long wait times and paperwork headaches. These days, most reputable suppliers maintain tight standards for traceability and batch documentation. That supports compliance in tightly regulated sectors like pharmaceuticals, where auditability is a daily concern.
Trying to substitute 4-Bromo-2-methylpyridine with alternate pyridines—say, swapping for 2-bromopyridine, or dropping the methyl entirely—usually means adjusting your plans. The absence of the methyl group changes electronic properties across the ring, impacting both reaction rates and selectivity. 2-Bromopyridine, while popular in some protocols, brings a different profile, lacking that fine-tuned control the methyl at position two provides.
Or consider 4-bromopyridine. It offers similar reactivity for coupling, but the lack of a methyl group removes certain directing abilities, so yields and product purity sometimes drop. Each of these analogs has a place in the chemist’s toolbox, but for projects aiming at specific substitution patterns or challenging selectivities, 4-Bromo-2-methylpyridine’s balance of reactivity and steric protection often leads to cleaner solutions, especially in aggregate during multistep syntheses.
Too often, ambitious teams get derailed by problems they didn’t anticipate—batch-to-batch variability among vendors, or mysterious byproducts from side reactions. Truth is, the finer details of the synthetic route can reveal more about your raw materials than a whole book of safety sheets or advertising copy. Over my years policing synthetic failures, pattern recognition matters: reliable sources build trust through documented purity, consistent melting points, and robust customer support.
Many seasoned procurement teams now focus on suppliers with transparent quality control, direct traceability to manufacturing lots, and credible certificates of analysis. This approach, built on evidence and experience, aligns perfectly with the expectations across industries. No chemist wants to compromise a development program with mystery materials; lives—and livelihoods—hang in the balance.
Environmental pressure increasingly shapes chemistry, affecting both workflow and innovation. Green chemistry now delivers more than lip service. Using selective, high-yielding intermediates such as 4-Bromo-2-methylpyridine shrinks waste and avoids unnecessary reagents. Multistep syntheses using poorly-chosen intermediates pile up excess solvents, toxic byproducts, and disposal costs.
Teams sensitive to sustainability turn to intermediates like this to speed up steps and cut out dead-ends. In my own work, I’ve observed process engineers streamline output by starting with a bromo-heterocycle that provides clean reactions under mild conditions. Simultaneously, predictable chemistry lends itself to automation, reproducible output, and compliance with ever-tightening environmental regulations.
The ongoing quest in chemical research always circles back to making synthesis smarter and more sustainable. 4-Bromo-2-methylpyridine underpins a growing family of methods favoring selectivity, efficiency, and modularity. Perhaps the excitement stems from watching new forms of cross-coupling push boundaries, relying on intermediates like this to unearth new types of chemical space. In graduate seminars, journal clubs, and even conference hallways, the next wave of discoveries will certainly lean on accessible, reliable building blocks.
More industries are starting to recognize the value in compounds that seem unremarkable at first glance. Dig beneath the surface, and 4-Bromo-2-methylpyridine proves itself indispensable, especially where intricate patterns on a pyridine core matter more than bulk or glamour. Over the last ten years, advances in process chemistry have brought this and similar intermediates closer to everyday use, slashing costs and removing barriers to entry for smaller firms eager to innovate.
In high-throughput screen settings, speed matters just as much as accuracy. Laboratories aiming to prototype new molecules across drug discovery, material development, or agrochemical design need flexible compounds that can stand up to a broad range of reaction conditions. 4-Bromo-2-methylpyridine regularly finds itself on these shelves.
For teams operating under time pressure, a trusted intermediate becomes more than just another reagent. Its consistent performance gives project managers confidence to commit to aggressive timelines. I’ve seen whole programs pivot on the reliability of a single reaction step, with tight delivery windows and resource constraints threatening to derail progress. With this compound, those stress tests often end in success rather than disappointment, allowing teams to push the boundaries further and faster without constantly troubleshooting reaction inconsistencies.
Despite all the clear advantages, challenges remain in raw material traceability, environmental impact, and long-term product stewardship. Leading practitioners have started to address these with smarter sourcing, deeper supplier partnerships, and transparent data sharing. In my experience, the best outcomes come from open dialogue between end-users and manufacturers, focusing not just on compliance but on practical questions—batch purity, shipment timelines, and the management of unwanted impurities or byproducts.
To address sustainability, more groups have begun to document and reduce waste at every scale, from milligram research reactions up to ton-scale manufacturing. Smart, modular processing relies on clean intermediates such as 4-Bromo-2-methylpyridine because each reagent that behaves as expected helps reduce resource consumption elsewhere in the process. Adopting best practices in packaging, minimizing exposure to the environment, and rethinking the logistics chain all contribute to more sustainable and safer outcomes.
Ongoing training builds a culture of safety and stewardship; personnel who understand the real nature of the reagents they work with spot issues faster and stay ahead of accidents. In my teams, regular workshops and refresher courses keep best practices front of mind, reducing both risk and waste. Sourcing only from suppliers willing to answer technical questions and provide verified supporting data keeps everyone accountable and informed.
The foundation laid by compounds like 4-Bromo-2-methylpyridine gives rise to progress in both routine and revolutionary directions. The modern chemical industry, often pushed by shifts in regulation and sustainability, thrives on inputs that behave predictably across a wide range of applications. The difference between success and a costly rerun can hinge on the choice of a single intermediate—the right fit for both the chemistry at hand and broader project goals.
In the past, difficulties in procurement or handling could shut down promising lines of inquiry before they got off the ground. Improved access, better cataloging, and clearer communication have smoothed the path for newer, smaller players, fostering more competition and creativity across the board. The upshot is a field enriched with possibility, grounded by a sense of responsibility not just for innovation but for the safety and sustainability of daily work.
Experience teaches that the success of a research program often depends more on reliable supply and deep understanding than on abstract molecular innovation alone. 4-Bromo-2-methylpyridine shines in this regard, not because of clever marketing or theory but by the results it delivers in countless applied settings. By sticking to well-characterized, consistently produced intermediates, both academic labs and large-scale manufacturers set themselves up for repeatable, credible results.
For anyone tackling complex new syntheses or navigating tight regulatory environments, few choices offer as much reassurance as a reagent proven by both time and experience. Trusted intermediates like this allow teams to look beyond the occasional hiccup, plan more ambitious projects, and ultimately deliver solutions with real impact. The future of chemistry, shaped by responsible sourcing and data-driven development, will continue to benefit from reliable partners like 4-Bromo-2-methylpyridine—a foundation not just for molecules, but for the people and ideas that bring research out of the lab and into the world.