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HS Code |
870528 |
| Iupac Name | 2-Bromo-5-(hydroxymethyl)pyridine |
| Molecular Formula | C6H6BrNO |
| Molecular Weight | 188.027 g/mol |
| Cas Number | 3430-19-7 |
| Appearance | White to off-white solid |
| Melting Point | 74-76 °C |
| Solubility In Water | Slightly soluble |
| Smiles | C1=CN=C(C=C1CO)Br |
| Inchi | InChI=1S/C6H6BrNO/c7-6-2-1-5(3-9)4-8-6/h1-2,4,9H,3H2 |
| Density | 1.68 g/cm³ (estimated) |
| Storage Conditions | Store at 2-8°C, keep tightly closed |
As an accredited 2-Bromo-5-(hydroxymethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | The 5g quantity of 2-Bromo-5-(hydroxymethyl)pyridine is supplied in a sealed amber glass vial with a secure screw cap. |
| Container Loading (20′ FCL) | 20′ FCL: Securely packed drums or containers, net weight approx. 10–14 MT, moisture and leakage protected, suitable for sea shipment. |
| Shipping | 2-Bromo-5-(hydroxymethyl)pyridine is shipped in tightly sealed containers to prevent moisture ingress and contamination. The packaging complies with relevant chemical transport regulations, ensuring safe handling. It is transported at room temperature, typically labeled as a hazardous material due to possible toxicity, requiring appropriate documentation and safety precautions during transit. |
| Storage | 2-Bromo-5-(hydroxymethyl)pyridine should be stored in a tightly closed container, protected from light and moisture. Keep it at room temperature in a cool, dry, and well-ventilated area, away from incompatible substances such as strong oxidizing agents. Ensure proper labeling, avoid exposure to heat or flame, and follow standard safety protocols for handling hazardous chemicals. |
| Shelf Life | 2-Bromo-5-(hydroxymethyl)pyridine should be stored tightly sealed, protected from light and moisture; typical shelf life is 2 years. |
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Purity 98%: 2-Bromo-5-(hydroxymethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and selectivity in target molecule formation. Melting Point 63–65°C: 2-Bromo-5-(hydroxymethyl)pyridine with a melting point of 63–65°C is used in solid-phase organic reactions, where it enables controlled reactivity and facile purification. Molecular Weight 188.03 g/mol: 2-Bromo-5-(hydroxymethyl)pyridine of molecular weight 188.03 g/mol is used in heterocyclic compound libraries, where it allows precise molecular design and diversity. Stability Temperature up to 120°C: 2-Bromo-5-(hydroxymethyl)pyridine stable up to 120°C is used in high-temperature coupling reactions, where it maintains structural integrity and consistent results. Particle Size <50 μm: 2-Bromo-5-(hydroxymethyl)pyridine with particle size below 50 μm is used in rapid dissolution formulations, where it provides enhanced solubility and homogeneous distribution. |
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2-Bromo-5-(hydroxymethyl)pyridine has worked its way into the lab routines of chemists who demand precision. For years, pyridine derivatives have shaped everything from environmental testing to drug development. I still remember the first time I handled this compound—its pale color and subtle crystalline form stood out from the shelves of similar reagents. What makes this particular molecule important lies not just in its structure, but in the possibilities it unlocks for experimental work and production processes.
2-Bromo-5-(hydroxymethyl)pyridine stands apart from the crowd thanks to the presence of both a bromo group and a reactive alcohol function on the pyridine ring. The positioning of these groups makes it an ideal building block in medicinal chemistry, especially as research teams continue chasing new routes to targeted molecules and analogs for pharmaceutical candidates. In my own experience, its predictable reactivity helps teams cut down on trial-and-error, letting the creative side of chemistry take charge without constant concern about purity variances.
Diving into the details, the molecular formula for 2-Bromo-5-(hydroxymethyl)pyridine is C6H6BrNO. The molecular weight clocks in near 188.03 g/mol, making it easy to handle in milligram to gram scales without tricky adjustment calculations. Purity levels usually exceed 98 percent by HPLC—one of the most reassuring guarantees for researchers focused on reproducibility. Analytical labs often use gas chromatography and NMR to confirm identity, and these standards ensure each bottle matches expectations batch after batch.
That said, not every supplier delivers the same performance. I’ve seen batches where moisture content or minute impurities led to stubborn side products during synthesis, raising costs in both time and materials. Good sourcing pays off. The best 2-Bromo-5-(hydroxymethyl)pyridine I’ve used always arrives as a white to off-white solid, which dissolves cleanly in polar organic solvents. The material doesn’t emit a strong odor, which translates to safer and more comfortable lab conditions.
2-Bromo-5-(hydroxymethyl)pyridine shows its true value as a versatile intermediate in organic synthesis. In my collaborations with pharmaceutical chemistry teams, this compound frequently served as a starting point for further substitutions. The bromine atom almost dares chemists to swap it out for more complex groups, expanding the family of pyridine-based drugs. At the same time, the hydroxymethyl group just begs to participate in etherifications, esterification, or oxidation.
Research into anti-infectives, agrochemicals, and fine chemical manufacturing leans on intermediates like this one for quick iteration. During scale-up runs, I’ve seen process chemists favor this compound thanks to its crystalline structure, which helps with weighing and transfer—reducing mess, errant dust, and lost yield. Its solubility profile means even aqueous extractions don’t strip it away too soon, and its stability at room temperature keeps it ready for bench work whenever new reactions come up.
A walk through most chemical catalogs uncovers dozens of pyridine derivatives, but 2-Bromo-5-(hydroxymethyl)pyridine draws particular attention for the deliberate placement of functional groups. Compounds like 2-bromopyridine lack the extra handle for derivatization, while 5-(hydroxymethyl)pyridine doesn’t offer a good target for halide exchange. The presence of both bromine and alcohol functions opens doors to Suzuki or Buchwald-Hartwig couplings, not just in small library syntheses but also in multi-step commercial processes.
In my own synthetic runs, choosing between this compound and its close cousins usually comes down to flexibility in modifications. If the research hinges on rapid diversification, 2-Bromo-5-(hydroxymethyl)pyridine brings more to the table. The difference might look minor on paper, but the choice can shave days off a medicinal chemistry campaign or make scale-up more predictable. The unique substitution pattern offers more synthetic branching points than either halogenated or simple alcohol pyridines alone.
Consistency in supply sometimes takes a hit, especially with disruptions in raw material markets. Anyone who’s worked in chemical procurement knows that the pain of waiting for a delayed shipment far outweighs the planning effort to maintain a small surplus. In tighter markets, pricing can swing upward—worth remembering for grant writers and project managers trying to stretch a research dollar.
A bigger headache comes with off-spec material. Impurities in halogenated pyridines can quickly poison catalysts or foul up analytical methods. Analytical teams in larger organizations routinely run quality control checks and push for detailed certifications. Smaller buyers don’t always get that luxury, which makes building a relationship with a responsive, transparent supplier one of the most important moves for keeping a research pipeline on schedule.
Daily handling doesn’t throw up too many red flags. The compound doesn’t dust up easily, so accidental inhalation isn’t a big concern compared to lighter, more powdery reagents. Proper gloves, standard lab coats, and a fume hood stay part of the routine, especially if reactions turn volatile. Storage calls for a capped bottle kept cool and dry. I’ve left it on the shelf for months with no signs of decomposition—none of the tell-tale color changes or caking that hint at hydrolysis or slow oxidation.
Waste management deserves a mention. Being a halogenated organic, spent residues usually end up in the halogenated waste stream. My first few reactions with this compound generated small amounts of organic solvent waste, and partnering with a professional disposal service made a difference to environmental compliance and lab safety standards. Environmental health and safety teams keep a close eye on any halogenated compound, so up-to-date documentation on handling and disposal gets priority in every lab notebook and protocol.
2-Bromo-5-(hydroxymethyl)pyridine sits among the unsung heroes that quietly support big advances. Its flexible functional groups turn up in patent literature on everything from kinase inhibitors to agricultural fungicides. I’ve watched research teams use it as an intermediate in route scouting—the early, experimental stages of process development—because it reacts cleanly and makes troubleshooting easier down the line.
Industrial-scale manufacturers have started favoring molecules like this for batch processing, where yield and efficiency drive every decision. In making active pharmaceutical ingredients (APIs), the bromine position gives an entry point for complexity, while the alcohol opens up further transformations. Upstream suppliers and contract manufacturing organizations praise consistent, high-purity lots for cGMP compliance. Quality assurance teams follow up with their own analysis, and repeatability rates make or break commercial viability.
Despite its advantages, not every lab can immediately switch workflows to leverage the dual reactivity here. Pricing sometimes reaches a premium, especially for small buyers without large volume contracts. Off-patent status means more players enter the fray, but competing for the best lots sharpens focus on trusted sources.
Another hurdle shows up in scale-up chemistry—those steps between grams and kilograms. Reactions that run smoothly at a few hundred milligrams might stall out when surface area, agitation, or heat transfer change. To keep yield and purity high, process chemists sometimes need to redesign purification steps or set up new crystallization protocols. My own transition from glassware to pilot plant included several iterations of process control, monitoring side-product formation, and keeping detailed process records in case revalidation was needed.
Colleagues in academia praise reliable sources of 2-Bromo-5-(hydroxymethyl)pyridine because of its well-documented properties and reproducibility. Published research includes spectral data, typical yields, and common by-products, making literature searches quicker when troubleshooting new routes. In teaching environments, advanced undergrad and graduate students learn the finer points of halide chemistry using well-characterized samples, building familiarity with tools and techniques that will later translate to industry settings.
Quality standards help anchor confidence in the resulting data. Rigorous analytical testing—NMR, mass spectrometry, elemental analysis—backs up research claims. As regulatory oversight grows stricter, documentation supporting every batch entry builds trust with both end users and regulatory agencies. The origin story of each shipment—lot numbers, storage histories, and purity certifications—feeds into batch records reviewed during audits.
Interest grows in green chemistry even for halogenated intermediates. Researchers look at ways to replace toxic solvents, use less energy-intensive conditions, and recover unreacted starting materials. My work with process engineers has shown that even modest improvements in recycling and energy management can make large differences in environmental footprint. Vendors that take extra steps with solvent recovery or adopt renewable energy in production attract a second look.
Sustainable production isn’t just a PR move—it’s a necessity as regulation tightens and customers hold suppliers to higher standards. Questions about carbon footprint and lifecycle management now appear right alongside standard inquiries about lead times and documentation. Chemistry students graduating today show a keen interest in environmentally responsible practices, which means the supply chain gets scrutinized both from a compliance perspective and a values-driven one.
Drawing from my own years in the field, a few strategies help address ongoing hurdles. Sourcing from multiple vetted suppliers—after running side-by-side quality checks—cuts down risk if any one pipeline dries up. Collaborating with analytical labs, especially those that embrace open communication, smooths over any doubts about minor batch variation.
Networking across industry conferences and digital spaces keeps information flowing about advances in safer handling, greener synthesis, and alternate raw materials. Some research groups now open their protocols to wider peer review, letting the broader scientific community weigh in on best practices. In the lab, regular training refreshers ensure everyone stays confident with handling, disposal, and workplace safety.
On the policy side, finding workable middle ground between cost and compliance matters more each year. Engaging early with regulators, auditors, and environmental health professionals helps teams prepare for future changes in reporting and documentation. Building a realistic cost model that accounts for both purchase price and waste disposal gives accounting teams a clearer picture of total outlay.
Years of experience with 2-Bromo-5-(hydroxymethyl)pyridine and similar intermediates have reshaped my view on what matters in a good reagent supplier relationship. Technical transparency, speed of communication, and willingness to update customers after issues mean more than the slickest website or lowest introductory offer. I once flagged an out-of-spec batch to a supplier—they shipped a replacement after county-level weather slowed their delivery, hats off to them for the quick recovery. Stories like that stick with experienced chemists and are passed around as teaching tools.
Teaching and mentoring new lab members, I always point out the little cues: color changes, packaging integrity, and the simplicity of recordkeeping that prevent mistakes later. Lab safety culture, too, relies on collective buy-in for good handling habits—gloves, eye protection, fume hoods, and safe storage never feel like overkill after you’ve seen even a minor spill spiral into a bigger clean-up.
At the end of the day, the value of a compound like 2-Bromo-5-(hydroxymethyl)pyridine comes down to reliability. Chemical research and production move fast, and no one wants to waste time questioning the basics. Trusted products free up mental energy for genuine innovation, deeper dives into new methodologies, and the satisfaction of seeing projects make it from whiteboard to real-world impact. I’ve worked with teams where everyone knew they could count on the quality, and that sense of peace let them focus on better science.
Future demands will only push for more robust, transparent sourcing and handling. Companies willing to share best practices, updates on sustainability initiatives, and clear records can look forward to stronger industry partnerships. New chemists entering the workforce bring fresh perspectives and sharpened ethical standards, enriching an already dynamic field. Staying informed, holding suppliers and colleagues accountable, and keeping an open mind all make a difference, not just for research outcomes but for long-term professional satisfaction.
As new discoveries keep rolling in and the demands on synthetic chemistry grow, attention lands on intermediates that open doors without adding unnecessary risk. In my work supporting pharmaceutical and chemical development, 2-Bromo-5-(hydroxymethyl)pyridine has shown itself to be a linchpin for efficient, flexible synthesis—never flashy, but always steady. It’s the sort of foundation upon which breakthroughs quietly build, one reaction at a time.