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HS Code |
988549 |
| Chemical Name | 2-(2-Bromoethyl)pyridine |
| Molecular Formula | C7H8BrN |
| Molecular Weight | 186.05 g/mol |
| Cas Number | 23831-32-5 |
| Appearance | Colorless to pale yellow liquid |
| Boiling Point | 84-85°C at 3 mmHg |
| Density | 1.43 g/cm³ |
| Refractive Index | 1.567 |
| Smiles | Brc1ccccn1CC |
| Purity | Typically ≥97% |
| Storage Conditions | Store at 2-8°C, protected from light and moisture |
| Solubility | Soluble in organic solvents such as dichloromethane, chloroform |
| Melting Point | - |
| Synonyms | 2-(2-Bromoethyl)pyridine, 2-Pyridylethyl bromide |
| Ec Number | 240-027-9 |
As an accredited 2-(2-Bromoethyl)pyridine factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | 2-(2-Bromoethyl)pyridine is supplied in a 25-gram amber glass bottle with a secure screw cap and hazard labeling. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL) for 2-(2-Bromoethyl)pyridine involves securely packing drums/pails to optimize space and ensure safe chemical transport. |
| Shipping | 2-(2-Bromoethyl)pyridine is shipped in tightly sealed containers under ambient conditions, protected from moisture and direct sunlight. Appropriate hazardous material labeling is applied, and transport complies with regulations for corrosive and environmentally hazardous substances. Ensure handling by trained personnel, and provide shipping documentation including safety data and emergency contact information. |
| Storage | 2-(2-Bromoethyl)pyridine should be stored in a tightly sealed container, in a cool, dry, and well-ventilated area, away from sources of ignition, heat, and incompatible substances such as strong oxidizers and acids. Protect from moisture and direct sunlight. Use appropriate chemical storage cabinets, and clearly label containers to prevent accidental misuse. Handle with proper personal protective equipment (PPE). |
| Shelf Life | 2-(2-Bromoethyl)pyridine is stable for at least 2 years when stored tightly sealed, in a cool, dry place, protected from light. |
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Purity 98%: 2-(2-Bromoethyl)pyridine with purity 98% is used in pharmaceutical intermediate synthesis, where it ensures high yield and selectivity in target compound formation. Molecular weight 202.06 g/mol: 2-(2-Bromoethyl)pyridine with molecular weight 202.06 g/mol is used in agrochemical research, where it allows accurate stoichiometric calculations for formulation development. Melting point 38-40°C: 2-(2-Bromoethyl)pyridine with melting point 38-40°C is used in fine chemical manufacturing, where it provides ease of handling during solid-state processing. Stability temperature up to 80°C: 2-(2-Bromoethyl)pyridine with stability temperature up to 80°C is used in chemical reaction optimization, where it maintains reactivity without decomposition under moderate heating. Low water content (<0.5%): 2-(2-Bromoethyl)pyridine with low water content (<0.5%) is used in moisture-sensitive organic synthesis, where it prevents undesired side reactions and product degradation. Density 1.52 g/cm³: 2-(2-Bromoethyl)pyridine with density 1.52 g/cm³ is used in liquid-liquid extraction protocols, where it enables efficient phase separation for downstream purification. Refractive index 1.578: 2-(2-Bromoethyl)pyridine with refractive index 1.578 is used in spectroscopic analysis, where it facilitates accurate purity and concentration measurements. Boiling point 220°C: 2-(2-Bromoethyl)pyridine with boiling point 220°C is used in high-temperature reaction systems, where it sustains chemical stability and minimizes loss by evaporation. |
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Modern chemistry never stands still, and the search for more reliable building blocks keeps growing. Every time I see a product like 2-(2-Bromoethyl)pyridine become available, I think of the long path researchers have taken to bring it to labs and industry floors. Over the years, chemists have turned small molecular tweaks into big advances, and this compound represents another step in that journey.
With a molecular weight clocking in near 200 grams per mole, 2-(2-Bromoethyl)pyridine often stands out from the crowd of pyridine derivatives. Its pale yellow to colorless oily appearance gives away its high purity status, which usually sits at or above 98 percent. Melting at near room temperature, typically under 30°C, its liquid state makes transfers and reactions much less frustrating than with sticky solids.
Some may see specifications as dry facts, but in practice, even a single percentage point of impurity can sabotage a whole batch. That’s why consistency in GC purity, stable batch-to-batch color, and clear documentation on moisture levels put this compound a notch above many off-brand bromoethyl alternatives.
2-(2-Bromoethyl)pyridine lands in a sweet spot for synthetic chemists. The bromoethyl side chain opens doors, acting as a reactive handle for coupling, substitution, or Grignard reactions. I remember back in grad school, tracking down an intermediate as flexible as this seemed impossible without running through toxic or sensitive reagents. Now, labs get to work with a single, well-defined molecule that reliably delivers its pyridine core to a huge range of transformations.
From my own experience, this intermediate rarely lets people down in pharmaceutical synthesis. One of its most common uses involves creating custom ligands—those compounds coordinating metals at the heart of complicated catalytic cycles. A clean, mono-brominated pyridine like this enables researchers to attach side groups only where desired, building more precise and efficient catalysts. Anyone who’s ever tried making a phosphine ligand by tedious multi-step synthesis knows the headache of mismatched isomers. With 2-(2-Bromoethyl)pyridine, functionalization happens where you want it, freeing up the workflow for more strategic thinking.
Chemists spoiled for choice have no shortage of pyridine derivatives to try, including 2-bromopyridine, 4-bromomethylpyridine, and a rainbow of alkylated pyridines. Picking the right one isn’t just about what’s available; it’s about reactivity and downstream compatibility. While 2-bromopyridine provides a simpler core, the ethyl chain on 2-(2-Bromoethyl)pyridine introduces a greater reach—fitting for applications demanding a little more distance between the ring and upcoming modifications.
Go for 2-chloroethylpyridine, and you dip into a territory with less leaving group ability and less predictable yields. Opt for a methyl instead of ethyl, and you’ll find sterics or solubility throw a wrench into some coupling reactions. In my own hands, the bromoethyl group quietly improves yields—small advantages that stack up into meaningful time and material savings.
This compound also side-steps some roadblocks inherent in branching or highly substituted analogs. Bulky substituents around the reactive site can slow down desired transformations, especially during N-alkylation or transition metal coupling. 2-(2-Bromoethyl)pyridine’s simple chain keeps those issues in check, giving it the edge for precise modification of complex frameworks. For medicinal chemists, pharmaceutical startups, or anyone scaling up to pilot production, those differences matter. It’s not just bench convenience—it’s project risk, regulatory compliance, and your team’s collective peace of mind.
Drug development leans on predictable intermediates, and this molecule offers exactly that. The pyridine motif shows up in countless approved drugs for its ability to disrupt pathogenic targets and maintain metabolic stability. The bromoethyl “arm” further expands possibilities, creating entry points for click chemistry, amide formation, and rapid library synthesis. Even in my earliest days running combinatorial chemistry screens, having modular intermediates like this sliced weeks off library assembly.
Researchers repeatedly cite the value of selective, high-yielding reactions. Using 2-(2-Bromoethyl)pyridine means spending less on purification and wasting fewer resources on by-product cleanup. No one wants to watch a promising lead evaporate in a haze of column chromatography and rotovap. Straightforward coupling to amines, thiols, and phosphines lets teams focus on SAR (structure-activity relationship) instead of solvent switches or endless pH adjustments.
Some may worry about the bromo group’s reputation as a possible alkylating hazard, but with the right handling, the benefits outweigh routine hazards. Proper ventilation, personal protective equipment, and thoughtful storage keep risks in check, mirroring practices already standard across synthetic chemistry labs worldwide.
Anyone who’s watched an R&D discovery falter during scale-up knows the pain of inconsistent supply or unreliable quality. Cheap, unvetted intermediates may look like a bargain for kilo-scale reactions, but a single contaminant or batch deviation can wipe out a campaign. With 2-(2-Bromoethyl)pyridine, reputable producers ensure batch audit trails, impurity profile disclosure, and reliable access to analytical data. This level of transparency was rare a decade ago—now, it’s non-negotiable for anyone shipping bulk intermediates across borders.
In my own projects, I’ve seen procurement teams pivot to compounds offering this kind of documentation precisely because regulatory environments turn stricter every year. Gone are the days of unlabelled bottles and one-off imports. The move toward tighter specifications and verifiable sources helps everyone—from pharma giants to contract manufacturers—avoid recalls, regulatory headaches, and ethical gray areas.
Because 2-(2-Bromoethyl)pyridine usually stays stable under cool, dry conditions, shelf life no longer becomes a guessing game. Tightly sealed packaging, matched with clear expiration dates, allows precise stock planning for large projects. Waste shrinks, costs drop, and staff get back more time for creative chemistry instead of endless solvent checks.
With sustainability on every industry agenda, intermediates like 2-(2-Bromoethyl)pyridine often attract questions. No single chemical intermediate unlocks all answers for greener chemistry, but making better choices at the supply level does ripple outward. Sourcing this compound from suppliers with traceable raw material chains and greener by-product control means less environmental baggage down the line. Demand for recycled or renewable raw materials is rising, and suppliers who respond build more trust with buyers—something worth encouraging in a field slow to embrace change.
I’ve seen students and industry colleagues alike challenge suppliers to reveal their waste disposal practices and resource sourcing. Such conversations weren’t happening two decades ago. Now, lab managers factor environmental performance into every purchasing decision. A cleaner process for producing 2-(2-Bromoethyl)pyridine—whether that means lower solvent consumption, reduced energy, or safer by-products—translates into a small but growing win for the broader chemical landscape.
Most standard textbooks mention a handful of approaches to prepare functionalized pyridines, but the actual route chosen shapes both cost and performance for end users. 2-(2-Bromoethyl)pyridine often starts life from a straightforward coupling of 2-vinylpyridine, followed by selective bromination. Older methods leaned on hazardous reagents or tedious purification, opening the door to low yields or tricky side-products.
Recent improvements in catalytic halogenation and milder reaction conditions changed the game. There’s much less mess, fewer headaches, and higher selectivity. The cleaner and more predictable approaches now on offer ensure lower levels of unwanted isomers or peroxide formation. Every chemist who’s had a reaction balloon out with side reactions learns quickly why reliable intermediates matter more than a few cents saved per gram.
It surprises many how much difference details in synthesis can make on product shelf life, color stability, or even reactivity. I’ve seen two suppliers offer ostensibly identical 2-(2-Bromoethyl)pyridine but deliver products that behave differently in scale-up or storage. Those invisible corners cut by the supplier become expensive problems downstream. Leaning on trusted partners and asking tough technical questions adds only a little at the start but saves wasted cycles of troubleshooting and rework.
Every organic chemist carries a catalog of “memorable” spills and endless safety briefings in the back of their mind. 2-(2-Bromoethyl)pyridine’s reputation as an alkylating agent means it owns a permanent spot on the “handle with care” list. Consistently tight caps, double containment, and labeled storage bins go a long way toward keeping labs safer. Anyone ignoring skin or respiratory precautions around this class of compounds tempts fate. My own close calls came early—skin contact once led to irritation that lingered for days.
Ventilation, gloves, and eye protection are non-negotiables. Solid spill kits and clear standard operating procedures saved my teams more than once. I’ve watched well-trained interns scatter in panic, and I’ve seen how a calm reminder about PPE and containment transforms emergencies into routine cleanups. Organizational memory—passing along lessons, not just procedures—sticks with teams much longer than endless posted warnings.
For large-scale users, air handling and effluent controls define the difference between a routine shift and a full-scale incident. Investment in closed transfer systems and building-level monitoring rarely shows up in boardroom slides, but every EHS (environment health and safety) professional knows the real savings turn up in avoided incidents and stable insurance costs.
No conversation about chemical intermediates feels complete without mentioning regulation. The rules keep shifting, from restricted substance lists to tighter tracking of dual-use chemicals. 2-(2-Bromoethyl)pyridine typically presents less regulatory complexity than controlled substances, but robust documentation keeps customs officials and compliance officers happy. As reporting requirements and data retention rules evolve, choosing well-documented supply partners saves more stress than many realize.
I’ve been burned by a missed update or two—shipments held for incomplete paperwork or ambiguous MSDS forms can freeze whole projects in place. Ensuring every jar or drum arrives with up-to-date safety, composition, and handling documents becomes an invisible force multiplier for global programs. Reliable suppliers make the difference, so picking those with a track record for quality control means fewer sleepless nights.
Price matters to buyers at all levels. Graduate students stretch grant budgets; procurement offices weigh cents per gram against downtime risk. Choosing a well-made intermediate like 2-(2-Bromoethyl)pyridine may cost a little more upfront, but anyone responsible for troubleshooting a bad batch knows which side to pick. A single contaminated drum can mean delayed launches, blown budgets, or regulatory headaches that last months.
I admit to occasionally chasing bargains down less-proven paths. Rarely did those gambles pay off. Waste disposal fees, analyst hours, and lost materials add up far faster than the cost difference between suppliers. For managers and teams where staff time comes at a premium, a few dollars’ savings on the catalog price quickly disappear in reruns, equipment decontamination, and morale loss. What counts is predictable performance, not just price tags.
Simple molecules sometimes become the seeds for genuine breakthroughs. The introduction of intermediates like 2-(2-Bromoethyl)pyridine to the commercial landscape means creative thinkers can test bold hypotheses without getting lost in supply or synthesis. In recent years, I’ve watched research speed jump as more labs gain access to reliable, specialty intermediates. Instead of custom-synthesizing every obscure building block, more teams now explore ideas right away, helping discoveries outpace bottlenecks.
The supply of well-characterized compounds also ripples into education. Undergraduate synthesis projects used to follow recipes from decades past; now, courses incorporate novel intermediates and push students to solve problems that matter—creating drug leads, sustainable materials, or new catalysts. That exposure to advanced building blocks accelerates learning and broadens the scope for the next wave of discoveries.
With chemistry so tightly tied to global health, food, and technology advances, every choice at the supply level multiplies downstream. Selecting intermediates like 2-(2-Bromoethyl)pyridine with documented origins and clean production histories shifts the baseline for everyone. I’ve witnessed firsthand how peer pressure among buyers moved supplier standards, resulting in universal benefits: less waste, easier audits, and happier end users.
As the catalogue of reliable, flexible intermediates continues to grow, new horizons open up for both discovery and industry. Experience in research, teaching, and industry keeps reinforcing the same lesson—a well-chosen building block like 2-(2-Bromoethyl)pyridine makes all the difference in outcomes and efficiency. Those who’ve juggled flawed intermediates know exactly how much time and sanity they’d trade for one less variable in the process.
What sets apart truly beneficial chemical intermediates isn’t a single standout feature, but the steady reliability provided during routine use. Open dialogue between chemists, procurement specialists, and suppliers leads to ongoing improvements—more data sharing, tighter specs, and clear documentation. Buyers who proactively ask about sourcing and batch testing, not just purity, nudge suppliers toward even better practices.
In my experience, collaborating with suppliers to improve packaging, address spills, or anticipate new regulatory trends led to smoother projects and happier teams. Informal networks, conference chats, and frank feedback shape today’s commercial standards. By sharing successes (and failures) openly, everyone gets a little smarter and the quality keeps rising.
2-(2-Bromoethyl)pyridine embodies the incremental advances that modern chemistry relies on. A molecule that opens doors, minimizes friction, and streamlines the journey from idea to impact. Whether in a university research group or a global pharmaceutical plant, it stands as a quiet catalyst for better science, safer processes, and more responsible industry practices.