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HS Code |
499608 |
| Productname | 2-Bromo-5-Chlorobenzyl Alcohol |
| Casnumber | 885521-34-0 |
| Molecularformula | C7H6BrClO |
| Molecularweight | 221.48 g/mol |
| Appearance | White to off-white solid |
| Meltingpoint | 62-66°C |
| Purity | Typically ≥97% |
| Solubility | Soluble in organic solvents such as DMSO and methanol |
| Smiles | OCc1cc(Cl)ccc1Br |
| Inchi | InChI=1S/C7H6BrClO/c8-6-2-1-5(4-10)3-7(6)9/h1-3,10H,4H2 |
| Storageconditions | Store at 2-8°C in a dry, well-ventilated place |
| Synonyms | 2-Bromo-5-chloro-benzylic alcohol |
As an accredited 2-Bromo-5-Chlorobenzyl Alcohol factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
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| Shipping | |
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New molecules don't show up in research labs or production lines by accident. People develop, test, and select them purposefully, building on what works. 2-Bromo-5-Chlorobenzyl Alcohol stands as a well-judged choice for teams aiming for reliable halogenated intermediates in both bench-scale research and larger pharmaceutical or agrochemical pipelines. The presence of bromine and chlorine atoms on the benzyl alcohol backbone opens interesting pathways for synthesis, especially for those chasing finely tuned molecular targets.
For me, hands-on work in organic labs underscored how halogen substituents steer reactivity. In 2-Bromo-5-Chlorobenzyl Alcohol, the position of the bromo and chloro groups at the 2 and 5 locations directly shapes its behavior. I’ve seen colleagues run into bottlenecks using less specialized intermediates. Either they'd get poor yields, or impurities would drown out the product. Swapping in a compound like this one often cleared the road because the positions of the halogens can push reactions where you want them—into unique coupling, substitution, and protection sequences that less sophisticated analogues can hardly match.
The product typically arrives as a white to pale solid, highlighting a purity that keeps downstream problems in check. Recent batches often meet or exceed 98% purity by HPLC analysis, an expectation rather than a label claim, and that’s something synthetic chemists and QA staff both keep a careful eye on. Structural formula: C7H6BrClO. Molecular weight clocks in at about 221.48 g/mol, which matters during scale-up and for those calculating reactant equivalence.
Storage stays simple: cool, dry, sealed away from oxidants. The compound’s melting point usually falls in a tight range between 70°C and 75°C, easing crystallization and purification planning.
My own exposure to benzylic alcohols came first as a student and then while supporting process chemistry teams. Benzyl alcohols as a class often pull extra duty as building blocks, but bringing in chlorine and bromine at precise spots gives room for much more. In medicinal chemistry, tweaking just one position can shift biological activity from weak to potent. 2-Bromo-5-Chlorobenzyl Alcohol lets chemists quickly install versatile groups, push cross-coupling reactions, and shape molecules that show antiviral, antibacterial, or even herbicidal properties.
In one project, we chased a set of derivatives targeting plant protection, and the bromo/chloro setup allowed modification at the 5-position that a plain benzyl alcohol couldn’t touch. Whether developing kinase inhibitors or working on seed coating actives, this compound opens doors. I’ve watched teams in the pharmaceutical sector lean on this product for library synthesis, while others in fine chemicals take it as a linker or a branching point toward larger scaffolds.
People sometimes overlook the gap between research and mass production. I’ve seen pilot plants bog down due to unpredictable intermediates, introducing delays and wasted resources. 2-Bromo-5-Chlorobenzyl Alcohol brings confidence when moving from a few grams in a hood to hundreds of kilos in a reactor. Good suppliers document impurity profiles and batch consistency, because nobody wants their API or active ingredient campaign derailed by a wild-card intermediate.
In pharmaceutical design, selectivity often matters more than anything else. The set-up of halogen groups on this molecule lets research chemists build custom aryl or alkyl derivatives with predictable regioselectivity. This control cuts down on failed experiments and surprise by-products, saving money and weeks of work.
Its use isn’t limited to end-stage drugs or crop additives. Research-scale teams tap this molecule for ligand synthesis, fluorescent probes, and as a partner for metal-catalyzed reactions. The alcohol can be oxidized cleanly, protected as an ether, or used in reductive aminations—so it fits multiple purposes in a sequence, not just a single niche.
Chemists rarely pick an intermediate because it’s new or trendy. It’s about reliability and how well it fits the synthetic plan. Other benzyl alcohols—like unsubstituted ones or those bearing only a single halogen—don’t offer the same reactivity profile. A simple benzyl alcohol works for protecting group chemistry, but falls short during iterative cross-coupling or challenging substitutions. Subtle tweaks, like adding a second halogen, bring new opportunities.
Take 2-Bromobenzyl Alcohol or 5-Chlorobenzyl Alcohol as examples. They each offer one reactive handle, but combining both on the same ring expands where reactions start and finish. Two halogen groups mean more routes for Suzuki or Heck coupling, and the selective activation of one position over another. You get more options, less waste of reagents, and less need for repeated purification.
Real value comes from choosing the best route, not just the most familiar one. The compound's unique set-up often bumps up overall process efficiency—a fact I’ve seen borne out in the yield tallies of multiple research teams.
Nobody wants a mystery substance showing up when a batch of a new drug calls for tight specifications. Routine analysis by NMR, HPLC, and mass spectrometry gives teams the transparency they count on. From a practical perspective, seeing a certificate of analysis for every lot—including impurity signatures and storage guidelines—builds trust between supplier and end user.
Handling halogenated organics asks for extra diligence. I’ve seen a few labs take shortcuts—short-lived time savers that led to costly cleanups or exposure risks. Safe handling protocols, PPE, and well-maintained ventilation are not optional here. The right approach limits hazards, protects staff, and keeps compliance officers off your back.
As environmental standards rise, waste solvent and halogen management become even more critical. I’ve worked with teams adapting new capture and recycling programs, using closed-loop systems where possible. The right chemical gives you control, but only if the supporting practices are just as robust.
Every research project and production run leans on trust and results. Time after time, bottlenecks crop up at the intersection of reliability, safety, and performance. I’ve watched new grads and senior scientists work faster and with more confidence using high-quality intermediates—2-Bromo-5-Chlorobenzyl Alcohol included—because known tools let you focus on the real unknowns: the chemistry you’re trying to unlock.
For teaching new researchers, there’s little substitute for seeing a reaction work as intended. Having material like this on hand means cleaner results and more meaningful troubleshooting. When the starting point is right, the outcome often falls into place with fewer headaches.
No compound operates in a vacuum—every chemical brings a footprint and a set of rules. This intermediate falls under various regional guidelines for handling halogenated aromatics. Regulations can shift, especially around waste management and worker exposure, so the best labs track MSDS updates closely. Working with halogenated compounds sometimes sparks hesitation due to perceptions about environmental risk. Fortunately, batch traceability, safer packaging, and smarter solvent handling keep the risks in check.
Technological growth in green chemistry means fewer emissions and less environmental harm than in years past. The realities of licensing, disposal, and recycling remain, but the right facilities handle such concerns with minimal fuss. Choosing intermediates designed for clean conversion and separations at scale plays into these efforts, cutting waste without slowing down progress.
Economic pressures can steer which intermediates get chosen—even influential pros sometimes pick based on short-term price over long-term value. With specialty compounds like 2-Bromo-5-Chlorobenzyl Alcohol, the discussion goes beyond sticker price. A mediocre substitute might seem frugal, but every failed run, lost day, or quality investigation brings costs in wasted starting materials, staff time, and missed deadlines.
Supply chain reliability also looms large. Juggling multiple suppliers for something as specialized as this invites delays or quality mismatches. From experience, teams hit fewer snags locking in with sources that show dependable lot-to-lot consistency, offer technical support, and keep thorough documentation on file.
Shortages of starting halides or fluctuating shipping timelines can ripple downstream. Seasoned buyers set up contingency planning for critical intermediates. Some labs stock extra reserves, weighing storage costs against the risk of running empty at the wrong moment. Others partner with regional distributors who can bridge supply gaps quickly.
Long-term lab managers know the value of giving new researchers a hands-on feel for reliable, well-understood compounds. A molecule like 2-Bromo-5-Chlorobenzyl Alcohol fits into this tradition. It allows trainees to see the impacts of substitution patterns on reactivity without the unpredictable quirks that come from less pure or inadequately characterized samples.
Workshops and advanced classes use this molecule to teach cross-coupling, protection and deprotection, and structure-activity relationships in medicinal chemistry. As a trainer, I found that being able to point out where a bromine or chlorine can be swapped—without scrambling for cleanup—built my students’ confidence. This builds stronger chemists, capable of innovation rather than just repetition.
Innovation speeds up every year, pushing research chemists and process engineers into faster cycles and higher expectations. Solid, versatile intermediates like 2-Bromo-5-Chlorobenzyl Alcohol support this push in tangible ways. They act as the pivot points around which custom syntheses, new drug candidates, and smart crop protectants turn.
I’ve seen pharmaceutical project leads relax a little when analytical data for a tricky intermediate checks out on the first run. Confidence in a batch means less troubleshooting and more productive hours. Likewise, industrial teams looking to trim waste appreciate the efficient reactivity this compound brings—it lets them get more out of each step, translating to leaner, smarter processes.
As digital tracking and real-time quality monitoring spread across industry, documentation and impurity mapping come standard. It’s no longer enough to simply have a material available; it must arrive with data, traceability, and evidence of sustainable practices.
Challenges remain, especially around halogen management and cost control. In my own project work, cost spikes for brominated aromatics sometimes forced teams to rethink entire synthetic sequences. Collaborative purchasing groups offer leverage for negotiation, while in-house recycling recovers value from spent materials. Many labs now invest in improved analytics to flag even faint impurities or supply inconsistencies, building more resilience into high-value project streams.
Teams working at scale sometimes run into bottlenecks with strict regulatory scrutiny or international shipping complications. Staying updated on changes in classification, labeling, and permissible exposure limits lets production continue without surprise interruptions. Back-up suppliers, strong supplier relationships, and digital inventory tracking round out a best-practice toolkit for minimal downtime.
In fast-paced research and development settings, dependable building blocks stretch budgets and speed up project timelines. This holds true across medicinal chemistry, agricultural innovation, and advanced materials discovery. 2-Bromo-5-Chlorobenzyl Alcohol offers the rare combination of flexibility, control, and proven compatibility with a sweeping range of synthetic targets.
I’ve watched diverse teams—from startup biotechs to established agrochemical producers—choose this intermediate when chasing higher yields, fewer purification steps, and more robust supply chains. Success hinges not only on cutting-edge ideas, but on steady hands and smart selections at every stage. Trustworthy intermediates form the backbone of real progress.
With new challenges and possibilities always arriving, the importance of carefully chosen, high-performing compounds will only grow. Researchers with hands-on experience and a practical mindset seek out products that save time, reduce risk, and keep discovery on track. For many, 2-Bromo-5-Chlorobenzyl Alcohol delivers exactly that.