|
HS Code |
964673 |
| Iupac Name | 3-Bromo-5-methylpyridine |
| Molecular Formula | C6H6BrN |
| Molar Mass | 172.02 g/mol |
| Cas Number | 3430-16-8 |
| Appearance | Colorless to pale yellow liquid |
| Density | 1.482 g/cm³ |
| Boiling Point | 204-206 °C |
| Melting Point | -13 °C |
| Refractive Index | 1.573 |
| Solubility In Water | Slightly soluble |
| Flash Point | 86 °C |
| Smiles | CC1=CC(N=CC1)=Br |
As an accredited 3-Bromo-5-methyl-pyridine 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 3-Bromo-5-methyl-pyridine, sealed with a screw cap, labeled with hazard and product information. |
| Container Loading (20′ FCL) | 20′ FCL container loaded with securely packaged 3-Bromo-5-methyl-pyridine drums, ensuring safe, efficient bulk chemical shipment. |
| Shipping | 3-Bromo-5-methyl-pyridine is shipped in tightly sealed, chemically resistant containers to prevent leaks and contamination. It is transported according to hazardous material regulations, with appropriate labeling. Handling requires gloves and eye protection. The package includes safety documentation and should be stored in a cool, dry place, away from incompatible substances. |
| Storage | 3-Bromo-5-methyl-pyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area away from sources of ignition. Keep it away from incompatible substances such as strong oxidizing agents. Store at room temperature, protecting it from moisture and direct sunlight. Ensure proper labeling and access only to trained personnel, following standard chemical storage protocols. |
| Shelf Life | 3-Bromo-5-methyl-pyridine is stable for at least 2 years when stored tightly sealed, protected from light, moisture, and heat. |
|
Purity 98%: 3-Bromo-5-methyl-pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and product purity. Melting Point 34-37°C: 3-Bromo-5-methyl-pyridine with a melting point of 34-37°C is used in custom organic synthesis, where it facilitates easy handling in processing stages. Molecular Weight 172.03 g/mol: 3-Bromo-5-methyl-pyridine with molecular weight 172.03 g/mol is used in agrochemical development, where it provides consistency in reaction stoichiometry. Stability Temperature up to 60°C: 3-Bromo-5-methyl-pyridine with stability temperature up to 60°C is used in industrial catalytic reactions, where it maintains chemical integrity under process conditions. Particle Size <150 µm: 3-Bromo-5-methyl-pyridine with particle size less than 150 µm is used in formulation of fine chemical blends, where it allows for improved homogeneity and reactivity. |
Competitive 3-Bromo-5-methyl-pyridine prices that fit your budget—flexible terms and customized quotes for every order.
For samples, pricing, or more information, please contact us at +8615371019725 or mail to sales7@boxa-chem.com.
We will respond to you as soon as possible.
Tel: +8615371019725
Email: sales7@boxa-chem.com
Flexible payment, competitive price, premium service - Inquire now!
In modern chemistry, reliable building blocks often determine the difference between wasted effort and a breakthrough discovery. 3-Bromo-5-methyl-pyridine isn’t just another reagent lost in a catalog — it proves its value for anyone pushing boundaries in pharmaceuticals, agrochemicals, and advanced materials. With a molecular formula of C6H6BrN and a balanced structure where the bromo and methyl groups sit on the pyridine ring, this compound shows just how much subtle tweaks can influence chemical behavior.
The bromo group brings more than just mass to the chain. It unlocks new possibilities for selective coupling, Suzuki reactions, and halogen substitution, all practical steps for synthesizing compounds people depend on every day. The methyl group, not to be underestimated, offers more than congestion or minor polarity shifts. From my own lab days, the difference even a single methyl group brings becomes obvious — separating tricky isomers or upping metabolic stability in drug candidates. That’s where 3-Bromo-5-methyl-pyridine steps apart from its simpler relatives, like plain 3-bromopyridine or just methylpyridine.
No one likes uncertainty in the flask or on the production line. Every lot of 3-Bromo-5-methyl-pyridine is meant to deliver clear results, plain and simple. Labs usually see this compound as a slight yellowish liquid with a distinct aromatic smell. Look for purity levels topping 98%, often confirmed with modern HPLC and GC traces. That’s because downstream issues cost time and money; a batch with too many side products drags down reaction yields, messes with purification, and lowers confidence in results. Chemists have long known the headaches of shortcutting on purity, so tight QA makes a world of difference. Rigorous controls during halogen exchange and purification keep essential characteristics stable from one bottle to the next.
Anyone who’s scaled up synthesis for industry knows unpredictability kills profit and timelines. 3-Bromo-5-methyl-pyridine saves on that learning curve. The aligned position of the bromine and methyl groups means fewer routes to side-products and cleaner, higher-yield reactions. Medicinal chemists, especially, appreciate the advantage during exploratory synthesis. It’s not about flash or gimmicks — it’s about grinding through library production with tools that simply work. Compare that process to more traditional reagents, which might require extra purification or protecting groups, and you see time savings add up.
Talking to trusted colleagues, performance isn’t about theoretical reactivity alone, either. It’s about how reagents behave over a long day: Isolating intermediates without degrading, storing for weeks without air sensitivity drama, and scaling from grams to kilos without odd batch-to-batch quirks. 3-Bromo-5-methyl-pyridine delivers, season after season, because the chemistry under the hood doesn’t leave you scrambling to patch problems. Shelf stability proves strong enough under standard storage — a cool, dry cabinet, nothing fancy.
The story doesn’t end at synthesis. 3-Bromo-5-methyl-pyridine’s performance stands out in real-world testing — especially during the construction of novel N-heterocycles, a backbone class in many drug molecules. Experienced process chemists note that some more exotic bromo-pyridines bring unpredictable byproducts or sluggish conversion. The methyl group at the 5-position, by contrast, gives just the push needed to dial in selectivity for cross-coupling or directed ortho-metalation. This is especially relevant in agrochemical research, where getting the right steric arrangement makes or breaks a new active ingredient.
Documentation in peer-reviewed publications backs up these experiences. Multiple syntheses of complex molecules have leaned on this compound to introduce halogenated pyridine units with predictable regioselectivity. For chemists looking for solid footing to launch new research or design next-generation products, this reagent’s profile helps sidestep the guesswork that plagues early-stage R&D.
Anyone outside the field might shrug at the difference between bromination at the 2, 3, or 4 position of the pyridine ring. Those in the business know how placement tweaks everything — from electronic behavior to biological properties. 3-Bromo-5-methyl-pyridine pushes reactivity in a controlled, repeatable way. You see fewer byproducts in coupling reactions, less scrambling during metalation, and improved ease at introducing complex fragments on the ring.
Standard bromo-pyridines have their use where ultimate simplicity is best. Still, for anyone needing a blend of reactivity, solubility, and selectivity, this compound proves its worth time and again. In medicinal chemistry, for example, researchers frequently use it for C–N or C–C bond formation, stepping away from more hazardous or less predictable aryl bromides. Using it shortens timelines, lowers cycle counts, and almost always delivers cleaner analytical results.
A decade ago, fine chemicals might have seemed the preserve of bench chemists or graduate students. That story’s different now. 3-Bromo-5-methyl-pyridine supports the manufacture of pharmaceutical intermediates and the synthesis of new crop protection agents alike. Screening campaigns, which demand large libraries of closely related molecules, often start off with pyridine scaffolds just like this one. It’s not just about convenience — regulatory filings or patent protection depend on reliable, reproducible starting materials. If a core reagent falls short, entire projects stall or fail regulatory review.
In my experience, pilot plants hit snags when a supposedly ‘routine’ batch arrives with subtle impurities or off-spec color. With high-purity lots, process engineers avoid weeks of headache. As a result, even small changes in the source or synthesis of raw materials ripple through entire product lines downstream. From a business standpoint, it makes sense to standardize on compounds where the evidence supports decades of reliable use, robust supply, and consistent documentation.
There’s no shortcut to experience in chemical sourcing. Try swapping in a similar aryl bromide for 3-Bromo-5-methyl-pyridine during a scale-up — sometimes it works, sometimes yields or purity drop off a cliff. No amount of theoretical modeling or supplier brochures quite replaces old-fashioned trial and error, so the value of sticking with a trusted scaffold becomes obvious. It’s not a matter of hype but of lived reality. When technical support teams troubleshoot stuck runs or mysterious peaks on the chromatogram, familiar compounds keep problems solvable.
3-Bromo-5-methyl-pyridine’s unique substitution pattern enables more than just academic novelty. Methyl groups at the 5-position influence lipophilicity and electronic distribution, meaning new derivatives show promise in both pharmaceutical and agrochemical screening. A solid body of literature supports its role as a key intermediate for kinase inhibitors, pesticide candidates, and novel fluorophores. This is not some speculative fringe — it’s a backbone of mainstream innovation in labs worldwide.
Day-to-day use calls for practical advice, not theoretical worries. Powdered gloves and well-fitting goggles, sure, but few special storage demands. Expect 3-Bromo-5-methyl-pyridine to hold up well in cool, dry, dark conditions, kept in tightly sealed glass. No reactive headaches with basic lab equipment. Accidental air exposure or brief light won’t trigger runaway degradation, which spares frantic after-hours cleanup or costly disposal. For larger-scale sites, standard stainless steel or glass-lined vessels suffice, reducing infrastructure upgrades or retrofitting costs.
In contrast, some less stable derivatives need excessive handling protocols, adding unnecessary expense and complexity. By sticking to established, robust reagents, companies avoid spikes in operating costs and can focus on results instead of compliance nightmares. For contract research and manufacturing organizations especially, compounds that repeatably meet quality metrics pay dividends through reduced waste and less extensive documentation.
Rising regulatory scrutiny means chemical producers can’t treat environmental and safety compliance as afterthoughts. Clear regulatory data and transparent safety practices distinguish 3-Bromo-5-methyl-pyridine from more exotic or poorly characterized alternatives. Safety data isn’t a formality — it guides ventilation setup, waste management, and the right emergency response plans. This is particularly important for companies preparing to launch new active pharmaceutical ingredients or crop protection products, where every reagent must face scrutiny from authorities worldwide.
Good suppliers demonstrate commitment to thorough documentation, from REACH dossiers to local waste disposal guidelines. My own collaborations with QA professionals have shown most problems stem from poorly tracked starting materials, not exotic process steps. Avoid regulatory gridlock by relying on compounds with well-annotated histories and trusted production pathways.
Plenty of bromo-pyridines crowd the chemical space, each with its own quirks. Some offer higher reactivity but pick up too many side reactions. Others boast lower cost but deliver headaches with inconsistent supply or impurities. The sweet spot with 3-Bromo-5-methyl-pyridine comes from its moderate electronic properties — neither overly reactive nor sluggish, and a balance of steric and electronic effects favoring clean transformations. Years of hands-on use make this balance clear across a range of reaction types, from Suzuki couplings to Buchwald-Hartwig aminations.
Switching to alternatives might shave a penny off up front, but time lost wrangling poor conversions or impure intermediates adds hidden costs. Compound libraries, especially, benefit from a stable, well-characterized core scaffold. This reduces analytical burden and assurance costs over thousands of samples.
Another practical point: derivatives with halogens at other ring positions often bring more regulatory hurdles, especially if historical toxicology data runs thin. Choosing a compound with a clean record speeds up product registration, especially for pharmaceutical and agrochemical launches.
The real world rarely offers perfect runs or zero waste. Labs face unexpected snags — product oils won’t crystallize, a coupling partner misbehaves, or an intermediate decomposes en route to the final target. With 3-Bromo-5-methyl-pyridine, practical experience shows solutions go further than reactivity tables suggest. Switching up bases or solvents, or dialing back catalyst amounts, usually gets things back on track. Instead of re-inventing the wheel, most teams find published protocols align closely with in-house SOPs, meaning troubleshooting takes hours, not weeks.
It’s not about eliminating failure entirely, but about reducing the hidden costs of uncertainty. That’s why successful labs and companies keep dependable reagents on hand for key transformations. Building institutional memory around trusted chemicals translates to smoother onboarding, faster project turnaround, and less staff turnover from burnout.
Pandemics, trade issues, and political shocks have all reminded the chemical world about supply chain fragility. Sourcing raw materials for specialized syntheses never used to occupy much brainspace, but recent disruptions flipped the script. Reliable, well-audited suppliers of 3-Bromo-5-methyl-pyridine now command a premium, simply because they save sleepless nights. Process development groups check for third-party impurity profiling and validated lot histories to avoid nasty surprises on delivery.
Prioritizing raw materials with a vetted supply chain shortens project timelines. Teams no longer get tied down chasing COAs or reverse-engineering upstream synthetic gaps. As projects scale, documented consistency at the early stages makes or breaks commercial launches. Anyone who’s sat through Friday afternoon meetings about unexpected supply hiccups knows the ripple effect a missing or sub-standard intermediate can create.
Facing rising demands in pharmaceutical development, green chemistry, or just keeping factories humming, every raw material pulls more weight than the price tag lets on. 3-Bromo-5-methyl-pyridine holds a small but important niche in this landscape. Its track record for reliability and practical handling makes it a valuable piece of the problem-solving toolkit.
Mentoring younger scientists through their first scale-up runs, I’ve seen how picking the right starting materials shapes both confidence and career outcomes. Standardizing on dependable, well-proven reagents isn’t just safe — it means teams can focus on innovation instead of firefighting. Adapting processes for new regulations, changing targets, or better sustainability often comes down to the simple question: Are the building blocks up to the task? In an age where speed and certainty rule, those sticking to proven standards like 3-Bromo-5-methyl-pyridine set themselves up for fewer sleepless nights, better productivity, and greater trust from clients and regulators alike.